EP1916991A1 - Cosmetically used cross-linked methyl methacrylate-copolymer - Google Patents

Abstract

The invention relates to cosmetic preparations containing at least one type of polymer A comprising polymerisable methyl methacrylate, methacrylic acid, acrylic acid and possibly at least one type of compound possibly provided with at least two double radically polymerisable, oleofinically unsaturated bonds and possibly with other oleofinically unsaturated compounds on the condition that the methacrylic acid weight amount is at least equal to the acrylic acid weight amount.

Description

Crosslinked methyl methacrylate copolymers for cosmetic applications

description

The present invention relates to cosmetic preparations containing at least one polymer A, the methyl methacrylate, b) methacrylic acid, c) acrylic acid, d) optionally at least one compound having at least two radically polymerizable, olefinically unsaturated double bonds and optionally further olefinic contains polymerized unsaturated compounds, with the Maßga- be that the amount by weight of component b) is at least equal to the amount by weight of component c).

State of the art

Stricter environmental regulations and growing ecological awareness increasingly demand ever lower levels of volatile organic compounds (VOCs) in cosmetic aerosol formulations such as aerosol hairsprays.

The VOC content in hair sprays is essentially determined by the non-aqueous solvents and the blowing agents. Therefore, instead of nonaqueous solvents, water is currently used as the solvent. However, this replacement of organic solvents brings with it some problems.

For example, formulations of the film-forming polymers known from the prior art which fulfill corresponding VOC requirements can not be sprayed or can be sprayed only after further dilution and are thus only conditionally suitable for use in hairsprays. Polymer films which are produced from such preparations do not have the necessary mechanical quality and therefore insufficient firming effect and poor hold for the hair.

WO 03/062288 and WO 03/061615 describe aqueous hair setting compositions containing an effective amount of a rheology modifying hair fixative associative polymer of an acid monomer and an associative monomer. As hydrophobic associative monomers, long-chain esters of (meth) acrylic acid are preferred. The polymers may contain other monomers and crosslinkers.

EP-A 0 184 785 describes an aqueous copolymer dispersion of 50-60% by weight of ethyl acrylate, 30-40% by weight of methacrylic acid, 5-15% by weight of acrylic acid and 0.02-0.04% by weight. % of a polyunsaturated copolymerizable monomer having a solids content of 5 to 30 wt .-%, which is suitable for thickening aqueous systems, in particular of hydrogen peroxide preparations, such as those used as developer formulations for oxidation hair dye and hair bleach. WO 95/05402 describes hair cosmetic preparations which comprise aqueous copolymer dispersions obtainable by copolymerization of 40 to 99% by weight of one or more water-insoluble, monoethylenically unsaturated monomers and 1 to 60% by weight of one or more water-soluble, monoethyl unsaturated monomers. Optionally, 0 to 30 wt .-% of one or more multiply ethylenically unsaturated monomers can be used.

DE 2 330 957 describes grafted and crosslinked cationic copolymers which are obtained by copolymerization of a) at least one cosmetic monomer, b) dimethylaminoethyl methacrylate, c) polyethylene glycol and d) a polyunsaturated crosslinking agent.

No. 4,543,249 describes non-aerosol compositions consisting of 1-10% by weight of a copolymer of 70-90% by weight of methyl methacrylate and 10-30% by weight of methacrylic acid, the carboxyl groups of the polymer being too 50 to 100% are neutralized with a water-soluble base and the polymer are dissolved in 65-99% ethanol.

DE-A 4327514 describes a fine, rapidly water-soluble polymer powder, composed of 30-99% by weight of units of alkali metal or preferably ammonium salts of (meth) acrylic acid, which may optionally be partially replaced by units of free (meth) acrylic acid, and 0.1-5% by weight of crosslinking monomer units and optionally up to 69.9% by weight of units of hydrophilic comonomers.

Task and solution

An object of the present invention was to provide polymers for cosmetic, in particular hair cosmetic preparations, which are well formulated as pump or aerosol spray in solvents or solvent mixtures with an increased water content, the formulations are well sprayable in the form of small uniform droplets and during and after Application as little as possible tend to foam and then formed films are not sticky and have good mechanical properties. In addition to the good compatibility with the usual cosmetic ingredients, the polymers applied to the hair should dry quickly and give the hair good consolidation and longer hold even in high humidity, have good washability and as optically clear VOC-55 aerosols (ie with a VOC - content of not more than 55% by weight). Furthermore, the treated hair should have good tactile properties such as a good touch.

These objects were surprisingly achieved by cosmetic preparations comprising at least one polymer A, which a) methyl methacrylate, b) methacrylic acid, c) acrylic acid, d) optionally at least one compound having at least two free-radically polymerizable, olefinically unsaturated double bonds and e) optionally further copolymerized olefinically unsaturated compounds, with the proviso that the amount by weight of the component b) at least equal to the amount by weight of component c).

In the context of the present invention, the term alkyl includes straight-chain and branched alkyl groups. Suitable short-chain alkyl groups are, for example, straight-chain or branched preferably C _r C ₆ alkyl and particularly preferably C ₄ - alkyl groups. These include in particular methyl, ethyl, propyl, isopropyl, n-butyl, 2-butyl, sec-butyl, tert-butyl, n-pentyl, 2-pentyl, 2-methylbutyl, 3-methylbutyl, 1, 2-dimethylpropyl , 1, 1-dimethylpropyl, 2,2-dimethylpropyl, 1-ethylpropyl, n-hexyl, 2-hexyl, 2-methylpentyl, 3-methylpentyl, 4-methylpentyl, 1, 2-dimethylbutyl, 1, 3-dimethylbutyl, 2 , 3-Dimethylbutyl, 1, 1-dimethylbutyl, 2,2-dimethylbutyl, 3,3-dimethylbutyl, 1,1,2-trimethylpropyl, 1,2,2-trimethylpropyl, 1-ethylbutyl, 2-ethylbutyl, 1 Ethyl 2-methylpropyl, n-heptyl, 2-heptyl, 3-heptyl, 2-ethylpentyl, 1-propylbutyl, octyl, etc.

Suitable longer-chain C ₈ -C ₃₀ -alkyl or C ₈ -C ₃₀ -alkenyl groups are straight-chain and branched alkyl or alkenyl groups. These are preferably predominantly linear alkyl radicals, as they also occur in natural or synthetic fatty acids and fatty alcohols and oxo alcohols, which may optionally be additionally mono-, di- or polyunsaturated. These include, for example, n-hexyl, n-heptyl, n-octyl, n-nonyl, n-decyl, n-undecyl, n-dodecyl ), n-tridecyl, n-tetradecyl, n-pentadecyl, n-hexadecyl, n-heptadecyl, n-octadecyl, n-nonadecyl etc. Cycloalkyl is preferably C ₅ -C ₈ -cycloalkyl, such as cyclopentyl, cyclohexyl, cycloheptyl or cyclooctyl.

The term heterocycloalkyl in the context of the present invention comprises saturated, cycloaliphatic groups having generally 4 to 7, preferably 5 or 6 ring atoms, in which 1 or 2 of the ring carbon atoms are replaced by heteroatoms selected from the elements oxygen, nitrogen and sulfur, and the optionally substituted, wherein in the case of a substitution, these heterocycloaliphatic groups 1, 2 or 3, preferably 1 or 2, particularly preferably 1 substituent selected from alkyl, aryl, COOR, COO M ⁺ and NE ¹ E ² , preferably alkyl, can carry. Exemplary of such heterocycloaliphatic groups are pyrrolidinyl, piperidinyl, 2,2,6,6-tetramethylpiperidinyl, imidazolidinyl, pyrazolidinyl, oxazo lidinyl, morpholidinyl, thiazolidinyl, isothiazolidinyl, isoxazolidinyl, piperazinyl, tetrahydrothiophenyl, tetrahydrofuranyl, tetrahydropyranyl, dioxanyl. Aryl includes unsubstituted and substituted aryl groups and is preferably phenyl, ToIyI, XyIyI, mesityl, naphthyl, fluorenyl, anthracenyl, phenanthrenyl, naphthacenyl and in particular phenyl, ToIyI, XyIyI or mesityl.

Substituted aryl radicals preferably have 1, 2, 3, 4 or 5, in particular 1, 2 or 3 substituents selected from alkyl, alkoxy, carboxyl, carboxylate, trifluoromethyl, - SO ₃ H, sulfonate, NE ¹ E ² , alkylene NE ¹ E ² , nitro, cyano or halogen. Hetaryl preferably represents pyrrolyl, pyrazolyl, imidazolyl, indolyl, carbazolyl, pyridyl, quinolinyl, acridinyl, pyridazinyl, pyrimidinyl or pyrazinyl.

Arylalkyl represents groups which contain both alkyl and aryl radicals, these arylalkyl groups being linked either via the aryl or via the alkyl radical to the compound carrying them.

Preferably contains polymer A, based on the total amount of components a) to e), 50-85, more preferably 65-80 and most preferably 70-80 wt .-% methyl methacrylate a) in copolymerized form.

Preferably contains polymer A, based on the total amount of components a) to e), preferably 1-30, more preferably 5-25 and most preferably 10-20 wt .-% of methacrylic acid b) in copolymerized form. The methacrylic acid can be present both in the form of the free acid and in the form of a cosmetically acceptable salt.

Cosmetically acceptable salts are, for example, the alkali metal or ammonium salts of methacrylic acid.

Preferably contains polymer A, based on the total amount of components a) to e), preferably 1-20, more preferably 3-15 and most preferably 5-10 wt .-% acrylic acid c) copolymerized. The acrylic acid can be present both in the form of the free acid and in the form of a cosmetically acceptable salt. Cosmetically acceptable salts are, for example, the alkali metal or ammonium salts of acrylic acid.

Optionally, polymer A contains at least one further compound d) copolymerized with at least two free-radically polymerizable, olefinically unsaturated double bonds. Preferably, the amount of this copolymerized component d), based on the total amount of components a) to e), 0-5, more preferably 0-4 and most preferably 0.5-3 wt .-%.

If appropriate, polymer A comprises further olefinically unsaturated compounds e) in copolymerized form. The amount of these at least one copolymerized component d) is preferably, based on the total amount of components a) to e), 0-30, particularly preferably 0-20 and very particularly preferably 0-14.5 wt .-%. Component d)

Component d) are compounds having at least two free-radically polymerizable, olefinically unsaturated double bonds per molecule. Such compounds are commonly referred to as crosslinkers. Free-radically polymerizable olefinically unsaturated double bonds are, for example, alkenyl groups which formally form by detachment of an H atom from an alkene. These include vinyl (-CH = CH ₂ ), 1-propenyl (-CH = CH-CH ₃ ), 2-propenyl or allyl (-CH ₂ -CH = CH ₂ ), 1-butenyl (-CH = CH-) CH ₂ -CH ₃ ) etc.

Also alkylidene groups, ie groups which are linked to a carbon atom of a molecule by a double bond, belong to the free-radically polymerizable, olefinically unsaturated double bonds (for example ethylidene: = CHCH ₃ ).

Suitable components d) are, for example, acrylic esters, methacrylic esters, allyl ethers or vinyl ethers of at least dihydric alcohols. The OH groups of the underlying alcohols may be completely or partially etherified or esterified; However, the components d) contain at least two olefinically unsaturated groups.

Examples of the underlying alcohols are dihydric alcohols such as 1, 2-ethanediol, 1, 2-propanediol, 1, 3-propanediol, 1, 2-butanediol, 1, 3-butanediol, 2,3-butanediol, 1, 4-butanediol , But-2-ene-1, 4-diol, 1, 2-pentanediol, 1, 5-pentanediol, 1, 2-hexanediol, 1, 6-hexanediol, 1, 10-decanediol, 1, 2-dodecanediol, 1 , 12-dodecanediol, neopentyl glycol, 3-methylpentan-1, 5-diol, 2,5-dimethyl-1,3-hexanediol, 2,2,4-trimethyl-1,3-pentanediol, 1,2-cyclohexanediol, 1 , 4-Cyclohexanediol, 1,4-bis (hydroxymethyl) cyclohexane, hydroxypivanic acid neopentyl glycol monoester, 2,2-bis (4-hydroxyphenyl) propane, 2,2-bis [4- (2-hydroxypropyl) phenyl] propane , Diethylene glycol, triethylene glycol, tetraethylene glycol, dipropylene glycol, tripropylene glycol, tetrapropylene glycol, 3-thio-pentane-1, 5-diol, and polyethylene glycols, polypropylene glycols and polytetrahydrofurans having molecular weights of 200 to 10,000.

In addition to the homopolymers of ethylene oxide or propylene oxide, it is also possible to use block copolymers of ethylene oxide or propylene oxide or copolymers which contain incorporation of ethylene oxide and propylene oxide groups. Examples of underlying alcohols having more than two OH groups are trimethylolpropane, glycerol, pentaerythritol, 1,2,5-pentanetriol, 1, 2,6-hexanetriol, triethoxycyanuric acid, sorbitan, sugars such as sucrose, glucose, mannose. Of course, the polyhydric alcohols can also be used after reaction with ethylene oxide or propylene oxide as the corresponding ethoxylates or propoxylates. The polyhydric alcohols can also be first converted by reaction with epichlorohydrin in the corresponding glycidyl ether.

Further suitable components d) are the vinyl esters or the esters of monohydric, unsaturated alcohols with ethylenically unsaturated C ₃ - to C ₆ -carboxylic acids, for example example, acrylic acid, methacrylic acid, itaconic acid, maleic acid or fumaric acid. Examples of such alcohols are allyl alcohol, 1-buten-3-ol, 5-hexen-1-ol, 1-octen-3-ol, 9-decen-1-ol, dicyclopentenyl alcohol, 10-undecen-1-ol, cinnamyl alcohol , Citronellol, crotyl alcohol or cis-θ-octadecen-i-ol. However, it is also possible to esterify the monohydric, unsaturated alcohols with polybasic carboxylic acids, for example malonic acid, tartaric acid, trimellitic acid, phthalic acid, terephthalic acid, citric acid or succinic acid.

Further suitable components d) are esters of unsaturated carboxylic acids with the polyhydric alcohols described above, for example oleic acid, crotonic acid, cinnamic acid or 10-undecenoic acid.

Also suitable as components d) are straight-chain or branched, linear or cyclic, aliphatic or aromatic hydrocarbons which have at least two double bonds which may not be conjugated to aliphatic hydrocarbons, e.g. Divinylbenzene, divinyltoluene, 1, 7-octadiene, 1, 9-decadiene, 4-vinyl-1-cyclohexene, trivinylcyclohexane or polybutadienes having molecular weights of 200 to 20,000.

Other suitable components d) are the acrylamides, methacrylamides and N-allylamines of at least dihydric amines. Such amines are, for example, 1,2-diaminomethane, 1,2-diaminoethane, 1,3-diaminopropane, 1,4-diaminobutane, 1,6-diaminohexane, 1,12-dodecanediamine, piperazine, diethylenetriamine or isophoronediamine. Also suitable are the amides of allylamine and unsaturated carboxylic acids such as acrylic acid, methacrylic acid, itaconic acid, maleic acid, or at least dibasic carboxylic acids, as described above.

Further, triallylamine and triallylmonoalkylammonium salts, e.g. Triallylmethylam- ammonium chloride or methyl sulfate, as components d) suitable.

Also suitable are N-vinyl compounds of urea derivatives, at least difunctional amides, cyanurates or urethanes, for example of urea, ethyleneurea, propyleneurea or tartaramide, e.g. N, N'-divinylethyleneurea or N, N'-divinylpropyleneurea. Also suitable are alkylenebisacrylamides such as methylenebisacrylamide and N, N '- (2,2-) butane and i.i'-bis- ^ S'-vinylbenzimidazolite ^ -on-J-i-butane.

Other suitable components d) are, for example, alkylene glycol di (meth) acrylates such as ethylene glycol diacrylate, ethylene glycol dimethacrylate, tetraethylene glycol acrylate, tetraethylene glycol dimethacrylate, diethylene glycol acrylate, diethylene glycol methacrylate, vinyl acrylate, allyl acrylate, allyl methacrylate, divinyldioxane, pentaerythritallyl ethers and mixtures of these components d).

Further suitable components d) are divinyldioxane, tetraallylsilane or tetravinylsilane. Particular preference is given to using components d) which are, for example, methylenebisacrylamide, triallylamine and triallylalkylammonium salts, divinylimidazole, pentaerythritol triallyl ether, N, N'-divinylethyleneurea, reaction products of polyhydric alcohols with acrylic acid or methacrylic acid, methacrylic acid esters and acrylic esters of polyalkylene oxides or polyhydric alcohols Ethylene oxide and / or propylene oxide and / or epichlorohydrin have been implemented.

Very particularly preferred as components d) are allyl methacrylate, pentaerythritol triallyl ether, methylenebisacrylamide, N, N'-divinylethyleneurea, triallylamine and triallyl monoalkylammonium salts, and acrylic esters of glycol, butanediol, trimethylolpropane or glycerol or acrylic esters of with ethylene oxide and / or Epichlorohydrin reacted glycol, butanediol, trimethylolpropane or glycerol.

Of course, it is also possible to use mixtures of the abovementioned compounds. Component d) is preferably soluble in the reaction medium. If the solubility of component d) in the reaction medium is low, it can be dissolved in a monomer or in a monomer mixture or else be metered in dissolved in a solvent which mixes with the reaction medium. Particularly preferred are those components d) which are soluble in the monomer mixture.

The components d), based on the total amount of the components a) to e) in amounts of 0 to 5 wt .-%, preferably 0 to 4 wt .-%, most preferably 0.1 to 3 wt .-% and in particular from 0.5 to 3 wt .-% used.

Component e)

Suitable components (e) are in general all radically polymerisable, olefinically unsaturated compounds which are different from components a) to d) and can be copolymerized with components a) to d).

Preferred components e) are e1) of b) and c) various anionic and anionogenic compounds e2) of a) various esters of (meth) acrylic acid e3) of e4) various amide group-containing compounds, e4) (meth) acrylamides, e5) cationogenic monomers , e6) cationic monomers

e1) of b) and c) various anionic and anionogenic compounds In the context of the present invention, an anionogenic compound is understood as meaning a compound which can be converted into the corresponding anionic form by deprotonation with customary, preferably cosmetically acceptable organic or inorganic bases. Components e1) are olefinically unsaturated, free-radically polymerizable carboxylic, sulfonic or phosphonic acids and their organic and inorganic salts.

Examples of preferred sulfonic acids are 2-acrylamido-2-methylpropanesulfonic acid (AMPS), styrenesulfonic acid, vinylsulfonic acid and salts thereof. Examples of preferred phosphonic acids are vinylphosphonic acid, 2-acrylamido-2-methylpropanephosphonic acid, allylphosphonic acid and salts thereof.

Component e1) is preferably selected from the group of olefinically unsaturated, free-radically polymerizable carboxylic acids and their organic and inorganic salts. The carboxylic acids may be monocarboxylic acids, dicarboxylic acids, carboxylic anhydrides or half esters of dicarboxylic acids.

Component e1) is particularly preferably selected from the group consisting of ethacrylic acid, alpha-chloroacrylic acid, crotonic acid, maleic acid, maleic anhydride, itaconic acid, citraconic acid, mesaconic acid, glutaconic acid, aconitic acid, fumaric acid, half esters of olefinically unsaturated dicarboxylic acids having 4 to 10, preferably 4 to 6 C atoms and their salts. e2) of a) various esters of (meth) acrylic acid

Component e2) is for example selected from the group consisting of ethyl (meth) acrylate, n-propyl (meth) acrylate, i-propyl (meth) acrylate, n-butyl (meth) acrylate, tert-butyl (meth) acrylate, i-butyl (meth) acrylate, sec-butyl (meth) acrylate, 2-pentyl (meth) acrylate, 3-pentyl (meth) acrylate, isopentyl (meth) acrylate, neopentyl (meth) acrylate, n- Octyl (meth) acrylate, 1, 1,3,3-tetramethylbutyl (meth) acrylate, ethylhexyl (meth) acrylate, n-nonyl (meth) acrylate, n-decyl (meth) acrylate, n-undecyl (meth) acrylate, tridecyl (meth) acrylate, myristyl (meth) acrylate, pentadecyl (meth) acrylate, PaI methyl (meth) acrylate, heptadecyl (meth) acrylate, nonadecyl (meth) acrylate, Arrachi- nyl (meth) acrylate, behenyl (meth) acrylate, lignocerenyl (meth) acrylate, cerotinyl (meth) acrylate, melissinyl (meth) acrylate, palmitoleinyl (meth) acrylate, o-leyl (meth) acrylate, linolyl (meth) acrylate, linolenyl (meth) acrylate , Stearyl (meth) acrylate, lauryl (meth) acrylate, phenoxyethyl (meth) acrylate, 4-t-butylcyclohexyl acrylate, cyclohexyl (meth) acrylate, ureido (meth) ac rylate, tetrahydrofurfuryl (meth) acrylate and mixtures thereof.

Component e2) may also be selected from esters of (meth) acrylic acid with alkanediols. For example, these are 2-hydroxyethyl (meth) acrylate, 2-hydroxyethyl methacrylate, 2-hydroxypropyl (meth) acrylate, 3-hydroxypropyl (meth) acrylate, 3-hydroxybutyl (meth) acrylate, 4-hydroxybutyl (meth) acrylate, 6-hydroxyhexyl (meth) acrylate, 3-hydroxy-2-ethylhexyl (meth) acrylate, neopentylglycol mono (meth) acrylate, 1,5-pentanediol mono (meth) acrylate and 1,6-hexanediol mono (meth) acrylate. Preferred (meth) acrylates are C ₂ -C ₀ -, more preferably C ₂ -C ₈ - and especially C ₂ -C ₄ - alkyl (meth) acrylates. Component e) can also be a mixture of methacrylates and acrylates. e3) of e4) various amide group-containing compounds

The amide group-containing compounds e3) are preferably selected from compounds other than e4) of the general formula VI

wherein R ^{1 is} a group of formula CH ₂ = CR ⁴ - with R ⁴ = H or dC ₄ alkyl and R ² and R ^{3 are} independently H, alkyl, cycloalkyl, heterocycloalkyl, aryl or hetaryl or R ² and R ³ together with the nitrogen atom to which they are attached represent a five- to eight-membered nitrogen heterocycle or R ^{2 represents} a group of the formula CH ₂ = CR ⁴ - and R ¹ and R ³ independently of one another represent H, alkyl , Cycloalkyl, heterocycloalkyl, aryl or hetaryl or R ¹ and R ³ together with the amide group to which they are attached represent a lactam having 5 to 8 ring atoms.

Preferred as component e3) are N-vinyllactams. Suitable components e3) are unsubstituted N-vinyllactams and N-vinyllactam derivatives which contain, for example, one or more C ₁ -C ₆ -alkyl substituents, such as methyl, ethyl, n-propyl, isopropyl, n-butyl, sec-butyl, tert. Butyl, etc., may have. These include, for example, N-vinylpyrrolidone, N-vinylpiperidone, N-vinylcaprolactam, N-vinyl-5-methyl-2-pyrrolidone, N-vinyl-5-ethyl-2-pyrrolidone, N-vinyl-6-methyl-2-piperidone , N-vinyl-6-ethyl-2-piperidone, N-vinyl-7-methyl-2-caprolactam, N-vinyl-7-ethyl-2-caprolactam, etc., and mixtures thereof. Preferred components e3) are those for which in formula VI R ^{2 is} CH ₂ = CH- and R ¹ and R ³ together with the amide group to which they are attached represent a lactam having 5 ring atoms.

Particular preference is given to using N-vinylpyrrolidone, N-vinylcaprolactam, N-vinylformamide, acrylamide or mixtures thereof, with N-vinylpyrrolidone being the most preferred. e4) (meth) acrylamides

Suitable components e4) are the amides of (meth) acrylic acid which are different from e5) and e6). Such amides are, for example, (meth) acrylamide, N-methyl (meth) acrylamide, N-ethyl (meth) acrylamide, Nn-propyl (meth) acrylamide, N-propyl (meth) acrylamide, N- (n-butyl) methacrylamide, N- (sec-butyl) methacrylamide, N- (tert-butyl) methacrylamide, N- (n-pentyl) (meth) acrylamide, N- (n-hexyl) (meth) acrylamide, N- (n-heptyl) (meth) acrylamide, N- (n-octyl) (meth) acrylamide, N- (t-octyl) (meth) acrylamide N- (1,1,3,3-tetramethylbutyl) ( nneth) acrylamide, N-ethylhexyl (meth) acrylamide, N- (n-nonyl) (meth) acrylamide _J N- (n-decyl) (meth) acrylamide _J N- (n-undecyl) (meth) acrylannide _J N- Tridecyl (meth) acrylannide, N-myristyl (meth) acrylannide, N-pentadecyl (meth) acrylamide, N-palmityl (meth) acrylannide, N-heptadecyl (meth) acrylamide, N-nonadecyl (meth) acrylamide, N-arrachinyl ( meth) acrylamide, N-behenyl (meth) acrylamide, N-lignocerenyl (meth) acrylannide, N-cerotinyl (meth) acrylamide, N-

Melissinyl (meth) acrylamide, N-palmitoleinyl (meth) acrylannide, N-oleyl (meth) acrylamide, N-linolyl (meth) acrylamide, N-linolenyl (meth) acrylamide, N-stearyl (meth) acrylamide, N-lauryl ( meth) acrylamide.

Suitable components e4) are furthermore 2-hydroxyethylacrylamide, 2-hydroxyethylmethacrylamide, 2-hydroxyethylethacrylamide, 2-hydroxypropylacrylamide, 2-hydroxypropylmethacrylannide, 3-hydroxypropylacrylamide, 3-hydroxypropylmethacrylamide, 3-hydroxybutylacrylamide, 3-hydroxybutylmethacrylamide, 4-hydroxybutylacrylamide, 4-hydroxybutylmethacrylamide, 6-hydroxyhexylacrylamide, 6-hydroxyhexylmethacrylannide, 3-hydroxy-2-ethylhexylacrylamide and 3-hydroxy-2-ethylhexylmethacrylamide.

e5) and e6) cationogenic and cationic monomers

The components e5) and e6) are monomers which contain at least one cationogenic and / or cationic group per molecule. A cationogenic group is understood as meaning a structural element which can be converted into the corresponding cationic form by protonation or quaternization. The cationogenic or cationic groups are preferably nitrogen-containing groups, such as primary, secondary and tertiary amino groups, and quaternary ammonium groups. Preferably, the nitrogen-containing groups are tertiary amino groups.

The components e5) and e6) are preferably used in an uncharged form for the polymerization. However, it is also suitable for use in charged form.

Charged cationic groups can be generated, for example, from the amine nitrogen atoms by protonation, for example with monohydric or polybasic carboxylic acids, such as lactic acid or tartaric acid, or mineral acids, such as phosphoric acid, sulfuric acid and hydrochloric acid. Preferably, the components e5) and e6) is selected from

Esters of .alpha.,. Beta.-olefinically unsaturated mono- and dicarboxylic acids with amino-alcohols, which may be mono- or dialkylated on the amine nitrogen, Amides of α, β-olefinically unsaturated mono- and dicarboxylic acids with diamines which have at least one primary or secondary amino group, N, N-diallylamine,

N, N-diallyl-N-alkylamines and their derivatives, - vinyl- and allyl-substituted nitrogen heterocycles,

- vinyl- and allyl-substituted heteroaromatic compounds and mixtures thereof.

Also suitable as components e5) and e6) are the esters of α, β-olefinically unsaturated mono- and dicarboxylic acids with aminoalcohols. Preferred amino alcohols are C ₂ -C ₂ -amino alcohols which are mono- or -dialkylated on the amine nitrogen CrC ₈ . As the acid component of these esters are z. For example, acrylic acid, methacrylic acid, fumaric acid, maleic acid, itaconic acid, crotonic acid, maleic anhydride, monobutyl maleate and mixtures thereof. Preference is given to using acrylic acid, methacrylic acid and mixtures thereof.

Particularly preferred as components e5) and e6) are N-methylaminoethyl (meth) acrylate, N-ethylaminoethyl (meth) acrylate, N- (n-propyl) aminoethyl (meth) acrylate, N- (n-butyl) aminoethyl (meth) acrylate, N- (tert-butyl) aminoethyl (meth) acrylate, N, N-dimethylaminomethyl (meth) acrylate, N ₁ N-dimethylaminoethyl (meth) acrylate, N, N-diethylaminoethyl (meth) acrylate, N ₁ N-

Dimethylaminopropyl (meth) acrylate, N, N-diethylaminopropyl (meth) acrylate, and N ₁ N- dimethylaminocyclohexyl (meth) acrylate.

In particular, the components e5) and e6) used are N- (tert-butyl) aminoethyl acrylate and N- (tert-butyl) aminoethyl methacrylate. Suitable components e5) and e6) are furthermore the amides of the abovementioned α, β-olefinically unsaturated mono- and dicarboxylic acids with diamines which have at least one primary or secondary amino group.

Preferred are diamines having a tertiary and a primary or secondary amino group. Preference is given as components e5) and e6) to N- [2- (dimethylamino) ethyl] acrylamide, N- [2- (dimethylamino) ethyl] methacrylamide, N- [3- (dimethylamino) propyl] acrylamide, N- [3-] (dimethylamino) propyl] methacrylamide, N- [4- (dimethylamino) butyl] acrylamide, N- [4- (dimethylamino) butyl] methacrylamide, N- [2- (diethylamino) ethyl] acrylamide, N- [4- (4- (dimethylamino) ethyl] acrylamide). dimethylamino) cyclohexyl] acrylamide and N- [4- (dimethylamino) cyclohexyl] methacrylamide. Particular preference is given to using N- [3- (dimethylamino) propyl] acrylamide and / or N- [3- (dimethylamino) propyl] methacrylamide. Suitable components e5) and e6) are furthermore N, N-diallylamines and N, N-diallyl-N-alkylamines and their acid addition salts. Alkyl is preferably C 1 -C ₂₄ -alkyl. Preference is given to N, N-diallyl-N-methylamine.

Suitable components e5) and e6) are also vinyl- and allyl-substituted nitrogen heterocycles, such as N-vinylimidazole, N-vinylimidazole derivatives, for. N-vinyl-2-methylimidazole, vinyl- and allyl-substituted heteroaromatic compounds such as 2- and 4-vinylpyridine, 2- and 4-allylpyridine, and the salts thereof.

Suitable components e5) and e6) are N-vinylimidazoles of the formula VII, wherein R ¹ to R ³ is hydrogen, C _r C ₄ alkyl or phenyl

Examples of compounds of general formula VII are shown in Table 1 below:

Table 1

Me = methyl; Ph = phenyl

The components e5) and e6) are particularly preferably selected from N- (tert-butylamino) ethyl (meth) acrylate, N, N-dimethylaminoethyl (meth) acrylate, N- [3- (dimethylamino) propyl] (meth) acrylamide , Vinylimidazole and mixtures thereof. If the polymers A according to the invention contain copolymerized components d3) and / or d4), they contain at least 0.1% by weight, preferably at least 1% by weight, more preferably at least 2% by weight and in particular at least 3% by weight. % and at most 30 wt .-%, preferably at most 20 wt .-%, more preferably at most 15 wt .-% and in particular at most 10 wt .-% of the components d3) and / or d4), based on the total weight of the components used a ) to d).

The charged cationic groups can be generated from the amine nitrogens by quaternization with so-called alkylating agents. Examples of suitable alkylating agents are C 1 -C ₄ -alkyl halides or sulfates, such as ethyl chloride, ethyl bromide, methyl chloride, methyl bromide, dimethyl sulfate and diethyl sulfate. Quaternization can generally be carried out both before and after the polymerization.

Also suitable as component e) are vinyl acetate, vinyl propionate, vinyl butyrate, ethylene, propylene, isobutylene, butadiene, styrene, α-methylstyrene, acrylonitrile, methacrylonitrile, vinyl chloride, vinylidene chloride, vinyl fluoride, vinylidene fluoride and mixtures thereof. The components e) may also contain silicone-containing structural elements.

Preparation of the polymers A according to the invention

The preparation of the polymers A according to the invention can e.g. by solution, precipitation, suspension or emulsion polymerization. Such methods are known in principle to the person skilled in the art.

Preference is given to the preparation by solution polymerization. It is preferred to prepare the polymers A by free-radical solution polymerization.

Preferred solvents for the polymerization are alcoholic or alcoholic / aqueous solvents such as ethanol and mixtures of ethanol with water and / or further alcohols such as methanol, n-propanol, isopropanol, n-butanol, sec-butanol, tert-butanol, n-hexanol and cyclohexanol and glycols such as ethylene glycol, propylene glycol and butylene glycol, and the methyl or ethyl ether of the dihydric Alcohols such as diethylene glycol, triethylene glycol, polyethylene glycols with number average molecular weights up to about 3000, glycerol and dioxane.

The polymerization in alcohol, for example in ethanol or in an alcohol / water mixture, for example in an ethanol / water mixture, is particularly preferred. The polymerization temperatures are preferably in a range of about 30 to 14O ⁰ C, more preferably 40 to 12O ⁰ C. The polymerization is usually carried out under atmospheric pressure, but it may also take place under reduced or elevated pressure. A suitable pressure range is between 1 and 5 bar.

Initiators For copolymerization, the monomers can be polymerized by means of radical-forming initiators.

As initiators for the radical polymerization, the peroxo and / or azo compounds customary for this purpose can be used, for example alkali metal or ammonium peroxydisulfates, diacetyl peroxide, dibenzoyl peroxide, succinyl peroxide, di-tert-butyl peroxide, tert-butyl perbenzoate, tert. Butyl perpivalate, tert-butyl peroxy-2-ethylhexanoate, tert-butyl permalate, cumene hydroperoxide, diisopropyl peroxidicarbamate, bis (o-toluoyl) peroxide, didecanoyl peroxide, dioctanoyl peroxide, dilauroyl peroxide, tert-butyl perisobutyrate, tert-butyl peracetate, di- tert-amyl peroxide, tert-butyl hydroperoxide, azobisisobutyronitrile, ^2,2'-azobis (2-amidinopropane) hydrochloride (Wako V-50 ^®), 2,2 ^1-azobis [2- (2-imidazolin-2-yl) propane] (Wako VA-061 ^®), 2,2'-azobis (2-methylbutyronitrile) (Wako V-59 ^®), dimethyl 2,2'-azobis (2-methyl propionate) (Wako V-601 ^®) , 2 _J 2'-azobis (2,4-dimethylvaleronitrile) _J i.i'-azobis-O-cyclohexanecarbonitrile), 4,4'-azobis (4-cyanovaleric acid) or 2- (carbamoylazo) iso butyronitrile.

Also suitable are initiator mixtures or redox initiator systems, such as. As ascorbic acid / iron (II) sulfate / sodium peroxodisulfate, tert-butyl hydroperoxide / sodium disulfite, tert-butyl hydroperoxide / sodium hydroxymethanesulfinate, H ₂ O ₂ ZCu ¹ , H ₂ O ₂ / ascorbic acid.

Suitable oxidizing agents for redox initiator systems are essentially the abovementioned peroxides. Suitable reducing agents may be sulfur compounds having a low oxidation state, such as alkali metal sulfites, for example potassium and / or sodium sulfite, alkali hydrogen sulfites, for example potassium and / or sodium hydrogen sulfite, alkali metal metabisulfites, for example potassium and / or sodium metabisulfite, formaldehyde sulfoxylates, for example potassium and / or sodium formaldehyde. sulfoxylate, alkali metal salts, especially potassium and / or sodium salts of aliphatic sulfinic acids and alkali metal hydrogensulfides, for example potassium and / or sodium hydrogensulfide, salts of polyvalent metals, such as iron (II) sulfate, iron (II)

Ammonium sulfate, iron (II) phosphate, endiols, such as dihydroxymaleic acid, benzoin and / or ascorbic acid, and reducing saccharides, such as sorbose, glucose, fructose and / or dihydroxyacetone. It may also be advantageous to use mixtures of water-soluble and less or not water-soluble initiators.

Suitable initiators are described in Chapters 20 and 21 of Macromolecules, Vol. 2, 2nd ed., H.G. Elias, Plenum Press, 1984, New York, incorporated herein by reference. Further, suitable photoinitiators are described in S.P. Pappas, J. Rad. Cur., Juicy 1987, p. 6, which is incorporated herein by reference.

The initiators are usually used in amounts of up to 10, preferably 0.02 to 5 wt .-%, based on the monomers to be polymerized. K value

The K value of the polymers is in the range from 15 to 120, preferably from 25 to 75 and more preferably from 25 to 55. Most preferred are K values in the range from 25 to 45 (determination according to Fikentscher, Cellulose Chemistry, Vol , Pp. 58-64 (1932)). Options for adjusting the K value of polymers to a value in a desired value range are known to the person skilled in the art. For example, these are the polymerization temperature, the amount of initiator or the use of chain transfer agents (regulators).

Chain Transfer Reagents To adjust the molecular weight, the polymerization can be carried out in the presence of at least one chain transfer agent. As a chain transfer agent, the usual, known in the art compounds such. B. sulfur compounds, for. For example, mercaptoethanol, 2-ethylhexyl thioglycolate, thioglycolic acid, alkanethiols, cysteine, acetylcysteine and Tribromchlormethan or other compounds that act Rule on the molecular weight of the resulting polymers are used.

The regulators are usually used in amounts of from 0.1 to 5% by weight, in particular from 0.25 to 2% by weight, based on the monomers to be polymerized. Usually, the regulators are added together with the monomers of the polymerization. polymerization

In order to obtain as pure as possible polymers A with a low residual monomer content, at least one postpolymerization step can follow the polymerization (main polymerization). The post-polymerization can be carried out in the presence of the same or a different initiator system as the main polymerization. The postpolymerization is preferably carried out at least at the same, preferably at a higher temperature than the main polymerization. If desired, the reaction mixture can be used after the polymerization or between the first and the second polymer. merisationsschritt be subjected to stripping with steam or a steam distillation.

The copolymerization is carried out by the usual techniques of solution polymerization, e.g. after the so-called batch polymerization, in which the monomers and, if appropriate, polymerization regulator and initiator are initially introduced in a solvent and heated to the polymerization temperature. The reaction mixture is preferably stirred at the polymerization temperature until the conversion of the monomers is more than 99.9%. If appropriate, the addition of the initiators in these processes can also take place only after the polymerization temperature has been reached.

Further process variants are feed methods which are preferably used. In this case, some or all of the reactants are added in whole or in part, batchwise or continuously, together or in separate feeds to a reaction mixture. Thus, for example, to a mixture of the monomers and a solvent at the polymerization temperature within a given time optionally a solution of the polymerization and an initiator solution continuously or batchwise. It. However, it is also possible to meter in a mixture of initiator and optionally regulator of the heated to polymerization temperature template. Another variant is to give the initiator below or at the polymerization temperature in the template and, if a regulator is to be used, only the regulator or a solution of the regulator after reaching the polymerization temperature within a given period of time to supply the reaction mixture.

The organic solvent used in the preparation of the polymers can by conventional, known in the art, for. B. by distillation at reduced pressure can be removed. The mixtures formed during the polymerization can be subjected to a physical or chemical aftertreatment following the polymerization process. Such processes are, for example, the known processes for reducing the residual monomer, for example the aftertreatment by addition of polymerization initiators or mixtures of several polymerization initiators at suitable temperatures or heating of the polymerization solution to temperatures above the polymerization temperature, aftertreatment of the polymer solution by means of steam or stripping with nitrogen or treating the reaction mixture with oxidizing or reducing reagents, adsorption processes such as the adsorption of impurities on selected media such as activated carbon or ultrafiltration. The known work-up steps may also be followed, for example suitable dry processes such as spray, freeze or drum drying or agglomeration processes subsequent to the drying. The low-residue mixtures obtained by the process according to the invention can also be marketed directly. Powdered polymers have the advantage of better shelf life, easier transportation and usually show a lower propensity for microbial attack.

Neutralization The polymers A according to the invention can be partially or completely neutralized. In particular, for the use of the polymers in hair cosmetic preparations, a partial or complete neutralization is advantageous. In preferred embodiments, the polymers are for example at least 10, preferably at least 30, more preferably at least 40, more preferably at least 50, most preferably at least 70 and in particular at least 95% neutralized.

In a most preferred embodiment, the polymers are at least 99% neutralized. Most preferably, the neutralization is at least 100%. The neutralization can take place during or after the polymerization.

It is furthermore advantageous if the neutralizing agent is added in more than equivalent amount, an equivalent amount being understood to mean the amount which is at least required in order to neutralize all neutralizable groups of the polymers. The neutralization can be done with, for example

a mono-, di- or trialkanolamine having 2 to 5 carbon atoms in the alkanol radical, which is optionally present in etherified form, for example mono-, di- and triethanolamine, mono-, di- and tri-n-propanolamine, mono-, di-, Di- and tri-isopropanolamine, 2-amino-2-methylpropanol and di (2-methoxyethyl) amine, - an alkanediolamine having 2 to 5 carbon atoms, for example 2-amino-2-methylpropane-1, 3-diol and 2-amino 2-ethyl-propane-1,3-diol, or

a primary, secondary or tertiary alkylamine having a total of 5 to 10 carbon atoms, for example N, N-diethylpropylamine or 3-diethylamino-1-propylamine.

Suitable alkali metal hydroxides for neutralization are, in particular, sodium hydroxide or potassium hydroxide and also ammonium hydroxide.

Often, good neutralization results are obtained with 2-amino-2-methylpropanol, triisopropanolamine, 2-amino-2-ethylpropane-1,3-diol, N, N-dimethylaminoethanol or 3-diethylamino-1-propylamine.

In a preferred embodiment of the invention, amines containing hydroxy groups for neutralization are selected from the group consisting of N ₁ N-

Dimethylethanolamine, N-methyldiethanolamine, triethanolamine, 2-amino-2-methyl-propanol and mixtures thereof. In this case, secondary or tertiary amino-bearing alkanolamines can show advantageous effects.

To neutralize the polymers in the preparations and compositions according to the invention, in particular amino-containing silicone polymers are suitable. Suitable silicone polymers comprising amino groups, for example, the silicone block copolymers of the aminopolyalkylene WO 97/32917, the products Silsoft ^® A-843 (dimethicone bisamino hydroxypropyl copolyol) and Silsoft ^® A-858 (trimethylsilyl A- modimethicone copolymer) (both Fa. Witco) , Furthermore, the neutralization polymers of EP-A 1 035 144 and in particular the silicone-containing neutralization polymers according to claim 12 of EP-A 1 035 144 are also suitable.

To increase the storage stability of the polymer solutions, it is advantageous to partially neutralize the polymers following the preparation. Particularly advantageous is a neutralization immediately after the polymerization in the range of 10 to 20 mol%, based on the total amount of acid groups.

Cosmetic preparations

The term VOC is known to the person skilled in the art. VOCs are organic chemical compounds which boil at atmospheric pressure in a range of up to approx. 260 ^° C. and thus can enter the ambient air in gaseous form. Volatile organic compounds include many solvents and blowing agents.

The polymers A described are outstandingly suitable for the production of cosmetic, in particular skin and / or hair cosmetic preparations. They serve, for example, as a polymeric film former. They can be used universally in a wide variety of cosmetic, preferably hair cosmetic preparations and formulated and compatible with the usual components.

The polymers A are advantageous for the production of elastic hairstyles with simultaneous strong consolidation (even at high humidity). The po- A polymers are distinguished by good propellant gas compatibility, good solubility in aqueous / alcoholic solvent mixtures, in particular by their suitability for use as optically clear low-VOC formulations and by good washability and combability without flaking effect. In addition, they improve hair treated with them in terms of its sensory properties such as grip, volume, handleability etc. Hairspray formulations based on the polymers A according to the invention are characterized by good sprayability and good rheological properties and extremely low tackiness of the resulting films. The cosmetic, preferably hair cosmetic preparations according to the invention containing the polymer A do not tend to foam after application. In addition to good compatibility with the usual cosmetic ingredients, the applied polymers A dry quickly.

Cosmetically Acceptable Carrier B) The cosmetic preparations according to the invention are preferably aqueous preparations which contain at least 10, preferably at least 20 and particularly preferably at least 30% by weight of water. The cosmetic preparations according to the invention preferably contain at most 80, preferably at most 55,% by weight of volatile organic constituents. In addition to water and the polymers A, the cosmetic preparations according to the invention furthermore have at least one cosmetically acceptable carrier B) which is selected from i) water-miscible organic solvents, preferably C ₂ -C ₄ -

Alkanols, in particular ethanol, ii) oils, fats, waxes, iii) of ii) various esters of C ₆ -C ₃₀ monocarboxylic acids with mono-, di- or trihydric alcohols, iv) saturated acyclic and cyclic hydrocarbons, v) fatty acids, vi) fatty alcohols, vii) propellants (propellant gases) and viii) mixtures thereof.

Suitable carriers B and further active ingredients and additives which are advantageously to be used are described in detail below.

Suitable cosmetically and pharmaceutically acceptable oil or fat components B) are described in Karl-Heinz Schrader, Fundamentals and formulations of cosmetics, 2nd edition, Verlag Hüthig, Heidelberg, pp. 319-355, to which reference is made here. The preparations according to the invention may comprise, for example, an oil or fat component B) which is selected from: hydrocarbons of low polarity, such as mineral oils; linear saturated hydrocarbons, preferably with more than 8 C Atoms such as tetradecane, hexadecane, octadecane, etc .; cyclic hydrocarbons, such as decahydronaphthalene; branched hydrocarbons; animal and vegetable oils; To grow; Wax esters; Petroleum jelly; Esters, preferably esters of fatty acids, such as. Examples are the esters of C 1 -C ₂₄ -monoalcohols with C 1 -C ₂₂ -monocarboxylic acids, such as isopropyl isostearate, n-propyl myristate, isopropyl myristate, n-propyl palmitate, isopropyl palmitate, hexacosanyl palmitate, octacosanyl palmitate, triacontanyl palmitate, dicron acontanyl palmitate, tetratriacontanyl palmitate, Hexancosanyl stearate, octacosanyl stearate, triacontanyl stearate, dotriacontanyl stearate, tetratriacontanyl stearate; Salicylates, such as d-Cio-salicylates, z. Octyl salicylate; Benzoate esters, such as C ₁ -C ₅ -alkyl benzoates, benzyl benzoate; other cosmetic esters, such as fatty acid triglycerides, propylene glycol monolaurate, polyethylene glycol monolaurate, C ₁ -C 8 -alkyl lactates, etc., and mixtures thereof.

Suitable silicone oils B) are z. As linear polydimethylsiloxanes, poly (methylphenylsiloxanes), cyclic siloxanes and mixtures thereof. The number average molecular weight of the polydimethylsiloxanes and poly (methylphenylsiloxanes) is preferably in a range from about 1000 to 150000 g / mol. Preferred cyclic siloxanes have 4- to 8-membered rings. Suitable cyclic siloxanes are, for. B. under the name cyclomethicone commercially available.

Preferred oil or fat components B) are selected from paraffin and paraffin oils; Petroleum jelly; natural fats and oils such as castor oil, soybean oil, peanut oil, olive oil, sunflower oil, sesame oil, avocado oil, cocoa butter, almond oil, peach kernel oil, castor oil, cod liver oil, lard, spermaceti, sperm oil, wheat germ oil, macadamia nut oil, evening primrose oil, jojoba oil; Fatty alcohols, such as lauryl alcohol, myristyl alcohol, cetyl alcohol, stearyl alcohol, oleyl alcohol, cetyl alcohol; Fatty acids such as myristic acid, stearic acid, palmitic acid, oleic acid, linoleic acid, linolenic acid and various saturated, unsaturated and substituted fatty acids; Waxes such as beeswax, carnauba wax, candililla wax, spermaceti and mixtures of the aforementioned oil or fat components.

Suitable hydrophilic carriers B) are selected from water, 1-, 2- or polyhydric alcohols having preferably 1 to 8 carbon atoms, such as ethanol, n-propanol, isopropanol, propylene glycol, glycerol, sorbitol, etc.

The cosmetic preparations according to the invention may be skin-cosmetic, hair-cosmetic or dermatological, hygienic or pharmaceutical preparations. Because of their film-forming and flexible properties, the polymers A described above are suitable, in particular, as additives for hair and skin cosmetics.

Preferably, the formulations according to the invention containing the polymers A are in the form of a spray, gel, foam, an ointment, cream, emulsion, suspension. sion, lotion, milk or paste. If desired, liposomes or microspheres can also be used.

The cosmetic compositions according to the invention preferably comprise at least one polymer A as defined above, at least one carrier B as defined above and at least one different constituent, which is preferably selected from cosmetically active ingredients, emulsifiers, surfactants, preservatives, perfume oils, thickeners, hair polymers, hair and skin conditioners, graft polymers, water-soluble or dispersible silicone-containing polymers, light stabilizers, bleaching agents, gelling agents, conditioners, colorants, tinting agents, tanning agents, dyes, pigments, bodying agents, moisturizers, backfats, collagen, protein hydrolysates, lipids, antioxidants, defoamers, antistatic agents, Emollients and plasticizers.

The preparations according to the invention preferably have a pH of from 2.0 to 9.3. Particularly preferred is the pH range between 4 and 8. As additional co-solvents may be organic solvents or a mixture of solvents having a boiling point below 400 ⁰ C in an amount of 0.1 to 15 wt.%, Preferably from 1 to 10 % By weight. Particularly suitable as additional co-solvents are unbranched or branched hydrocarbons such as pentane, hexane, isopentane and cyclic hydrocarbons such as cyclopentane and cyclohexane. Further, particularly preferred water-soluble solvents are glycerol, ethylene glycol and propylene glycol in an amount of up to 30% by weight.

In a preferred embodiment of the invention, the preparations according to the invention have a proportion of volatile organic components of at most 80% by weight, preferably at most 55% by weight and in particular at most 35% by weight. A preferred article are thus cosmetic, preferably hair cosmetic preparations that comply with the Iow VOC standard, ie VOC 80 or VOC 55 standard.

Preference is given to the use of the polymers A, in particular in hair spray preparations which comprise the following constituents: partially or completely neutralized polymer A according to the invention;

- Water;

- cosmetically customary organic solvents such as, for example, ethanol, isopropanol and dimethoxymethane, but also acetone, n-propanol, n-butanol, 2-methoxypropan-1-ol, n-pentane, n-hexane, cyclohexane, n-heptane, n - octane or dichloromethane or mixtures thereof;

cosmetically customary propellant, for example n-propane, isopropane, n-butane, i-butane, 2,2-dimethylbutane, n-pentane, isopentane, dimethyl ether, difluoroethane, fluorotrichloromethane, dichlorodifluoromethane or dichlorotetrafluoroethane, HFC-152A (1,1-difluoroethane), HFC-134a (1,1,2,2-tetrafluoroethane), N ₂ , N ₂ O and CO or mixtures thereof.

To neutralize the polymers A according to the invention and to adjust the pH of the cosmetic, preferably hair cosmetic preparations, alkanolamines are advantageously used. Examples (INCI) are aminomethylpropanol, diethanolamines, diisopropanolamines, ethanolamines, methylethanolamines, N-lauryldiethanolamines, triethanolamines, triisoproanolamines, etc. It is possible to use both alkanolamines carrying primary amino groups and secondary amino groups. In addition, alkali hydroxides (e.g., NaOH, preferably KOH) and other bases may be used for neutralization (e.g., histidine, arginine, lysine or ethylenediamine, diethylenetriamine, melamine, benzoguanamine). All of the bases given may be used alone or in admixture with other bases to neutralize acidic cosmetic products. In a preferred embodiment of the invention, amines containing hydroxy groups for neutralization are selected from the group consisting of N, N-dimethylethanolamine, N-methyldiethanolamine, triethanolamine, 2-amino-2-methylpropanol and mixtures thereof.

In this case, secondary or tertiary amino groups bearing alkanolamines can show advantageous effects.

Accordingly, an object of the present invention is aqueous cosmetic, preferably skin and / or hair cosmetic preparations which, in addition to the at least one polymer A and the carrier B, have at least one active substance or additive selected from the group consisting of viscosity-modifying substances, hair-care substances, hair-setting substances, silicone compounds, light stabilizers, fats, oils, waxes, preservatives, pigments, soluble dyes, particulate matter, and surfactants.

Hair cosmetic formulations according to the invention contain in a preferred embodiment

i) 0.05 to 20% by weight of at least one polymer A, ii) 20 to 99.95% by weight of water and / or alcohol, iii) 0 to 50% by weight of at least one propellant gas, iv) 0 to 5% by weight of at least one emulsifier, v) 0 to 3% by weight of at least one thickener, and vi) up to 25% by weight of further constituents.

Under alcohol are all of the aforementioned, customary in cosmetics alcohols to understand z. For example, ethanol, isopropanol, n-propanol. Propellant (propellant gases)

As propellants (propellants) come from said compounds, especially the hydrocarbons, in particular propane, n-butane, n-pentane and mixtures thereof and dimethyl ether and difluoroethane for use. Optionally, one or more of said chlorinated hydrocarbons are used in blowing agent mixtures, but only in small amounts, for example up to 20 wt .-%, based on the blowing agent mixture.

The cosmetic, preferably hair cosmetic preparations according to the invention are also particularly suitable for pump spray preparations without the addition of propellants or else for aerosol sprays with customary compressed gases such as nitrogen, compressed air or carbon dioxide as propellant.

For example, a standard aqueous aerosol spray formulation includes the following ingredients: ■ 100% neutralized polymer A

^■ Alcohol

■ Water

Dimethyl ether and / or propane / n-butane and / or propane / isobutane,

In this case, the total amount of the volatile organic components is preferably at most 80, more preferably at most 55 wt .-% of the preparation.

The cosmetic, preferably hair cosmetic preparations according to the invention preferably comprise at least one polymer A according to the invention, at least one cosmetically acceptable carrier B as defined above and at least one further active ingredient or additive which is selected from cosmetically active ingredients, emulsifiers, surfactants, preservatives , Perfume oils, thickeners, hair polymers, hair conditioners, graft polymers, water-soluble or dispersible silicone-containing polymers, light stabilizers, bleaches, gelling agents, conditioners, colorants, tinting agents, tanning agents, dyes, pigments, bodying agents, moisturizers, backfats, collagen, egg white hydrolysates, lipids, antioxidants Defoamers, antistatic agents, emollients, lanolin components, protein hydrolysates and plasticizers.

Other polymers

For the targeted adjustment of the properties of cosmetic, preferably hair-cosmetic preparations, it is often advantageous to use the polymers of the invention in admixture with other (hair) cosmetically customary polymers.

In a further preferred embodiment, the agent according to the invention contains 0.01 to 15% by weight, preferably 0.5 to 10% by weight, of at least one further synthetic thetic or natural nonionic, preferably a film-forming polymer. Natural polymers are also understood to mean chemically modified polymers of natural origin. Film-forming polymers are polymers which, when used in 0.01 to 5% strength aqueous, alcoholic or aqueous-alcoholic solution, are able to deposit a polymer film on the hair.

As such other conventional polymers are, for example, anionic, cationic, amphoteric, zwitterionic and neutral polymers.

Examples of such other polymers are

Copolymers of ethyl acrylate and methacrylic acid - copolymers of N-tert-butylacrylamide, ethyl acrylate and acrylic acid

polyvinylpyrrolidones

- Polyvinylcaprolactams

- Polyurethanes

Copolymers of acrylic acid, methyl methacrylate, octylacrylamide, butylaminoethyl methacrylate and hydroxypropyl methacrylate,

Copolymers of vinyl acetate and crotonic acid and / or (vinyl) neodecanoate, copolymers of vinyl acetate and / or vinyl propionate and N-vinylpyrrolidone,

carboxy-functional copolymers of vinylpyrrolidone, t-butyl acrylate, methacrylic acid, copolymers of tert-butyl acrylate, methacrylic acid and dimethicone copolyol.

Surprisingly, it has been found that cosmetic and preferably hair cosmetic preparations containing the polymers A in combination with other polymers have unexpected properties. The cosmetic and preferably hair cosmetic preparations according to the invention are superior to the preparations of the prior art, in particular with regard to the totality of their cosmetic properties.

Copolymers of ethyl acrylate and methacrylic acid (INCI name: Acrylates Copo- lymer), are available, for example, as commercial products Luviflex Soft ^® (BASF).

Copolymers of N-tert-butylacrylamide, ethyl acrylate and acrylic acid (INCI designation voltage: Acrγlates / Acrγlamide copolymer) are available for example as commercial products Ultrahold ^® strand, Ultrahold 8 ^® (BASF).

Polyvinylpyrrolidones (INCI name: PVP) are available for example under the trade names Luviskol ^® K, Luviskol ^® K30 (BASF) and PVP K ^® (ISP).

Polyvinylcaprolactams (INCI: Polyvinylcaprolactams) are for example available under the trade name Luviskol Plus ^® (BASF). Polyurethanes (INCI: Polyurethane-1) are for example available under the trade name Luviset ^® PUR.

Copolymers of acrylic acid, methyl methacrylate, octyl acrylamide, Butylaminoethylmethylacrylat, hydroxypropyl methacrylate (INCI: Octylacrylamide / Acrylates / Butylaminoethyl Methacrylate Copolymer) are known for example under the trade name Amphomer ^® 28-4910 and Amphomer ^® LV-71 (National Starch).

Copolymers of vinyl acetate and crotonic acid (INCI: VA / crotonates / copolymer) are available for example under the trade name Luviset ^® CA 66 (BASF), Resyn ^® 28-1310 (National Starch), Gafset ^® (GAF) or Aristoflex ^® A (Celanese) , Copolymers of vinyl acetate, crotonic acid and (vinyl) neodecanoate (INCI:

VA / Crotonates / Neodecanoate Copolymer) are available for example under the trade name Resyn ^® 28-2930 (National Starch) and Luviset ^® CAN (BASF).

Copolymers of vinyl acetate and N-vinylpyrrolidone (INCI: PVP / VA) are available for example under the trade name Luviskol VA ^® (BASF), and PVP / VA (ISP). Carboxy-functional copolymers of vinylpyrrolidone, t-butyl acrylate, methacrylic acid are available for example, under the trade name Luviskol ^® VBM (BASF).

Copolymers of tert-butyl acrylate, methacrylic acid and dimethicone copolyol are available for example, under the trade name Luviflex Silk ^® (BASF).

Suitable anionic polymers are homopolymers and copolymers of acrylic acid and methacrylic acid or salts thereof, copolymers of acrylic acid and acrylamide and salts thereof, sodium salts of polyhydroxycarboxylic acids, copolymers of acrylic acid and methacrylic acid with, for example, hydrophobic monomers, for example C ₄ - acrylic acid alkyl esters C ₃₀ -alkyl (meth) C ₄ -C ₃₀ - alkyl vinyl ester, C ₄ -C ₃₀ -alkyl and hyaluronic acid, and further, under the trade names Amerhold ^® DR-25, Ultrahold ^®, Luviset ^® PUR, Acronal ^® Acudyne ^{®, ®} Lovocryl, Versatyl ^®, Amphomer ^® (28-4910, LV-71), Placise ^® L53, Gantrez ^® ES 425, Advantage Plus ^®, Omnirez ^® 2000, Resyn ^® 28-1310, Resyn ^® 28-2930, balance ^® (0/55) Acudyne 255 ^®, Aristoflex ^® A or Eastman AQ ^® known polymers.

Furthermore, for example, the group comprising the polymers suitable Balance CR ^® (National Starch), Balance ^® 47 (National Starch; octylacrylamide / acrylates / butylaminoethyl methacrylate copolymer), Aquaflex ^® FX 64 (ISP; isobutylene / ethylmaleimide / hydroxyethyl thylmaleimid copolymer) Aquaflex ^® SF-40 (ISP / National Starch; VP / vinyl caprolactam / DMAPA acrylates copolymer), Alliance ^® LT-120 (ISP / Rohm &Haas; acrylates / C1-2 succinate / hydroxyacrylate copolymer) Aquarez ^® HS (Eastman, polyester-1). And the polymers under the trade names Diaformer ^® suitable Z-400 (Clariant; methacryloylethylbetaine / methacrylate copolymer), Diaformer ^® Z-711 (Clariant; methacrylates loylethyl N-oxide / methacrylate copolymer), Diaformer ^® Z-712 (Clariant ; methacryloylethyl N-oxide / methacrylate copolymer), Omnirez ^® 2000 (ISP; monoethyl ester of polyvinyl poly (methyl vinyl ether / maleic acid in ethanol), Amphomer ^® HC (National Starch; acrylate / octylacrylamide copolymer), Amphomer ^® 28-4910 (National Starch; octylacrylamide / acrylate / butylaminoethyl methacrylate copolymer), Advantage ^® HC 37 (ISP; terpolymer of vinylcaprolactam / vinylpyrrolidone / dimethylaminoethyl methacrylate), Advantage ^® LC55 and LC80 or LC A and LC e, Advantage ^® Plus (ISP; VA / butyl ma- leate / isobornyl acrylates copolymer), Aculyne ^® 258 (Rohm &Haas; acrylate / hydroxy - ester acrylate copolymer), Luviset ^® PUR (BASF, polyurethane-1), Eastman ^® AQ 48 (Eastman), Styleze ^® CC-10 (ISP, VP / DMAPA Acrylates copolymer), Styleze ^® 2000 (ISP; VP / Acrylates / lauryl Methacrylate copolymer), DynamX ^® (National Starch; Polyu- Rethane-14 AMP-Acrylates copolymer), Resyn ^® XP (National Starch; Acrylates / octylacrylamide copolymer), Fixomer ^® A-30 (Ondeo Nalco, polymethacrylic acid (and) acrylamidomethylpropane sulfonic acid), Fixate G-100 ^® (Noveon; AMP-Acrylates / allyl Methacrylate C opolymer).

Suitable polymers are also copolymers of (meth) acrylic acid and polyether acrylates, wherein the polyether chain is terminated with a C ₈ -C ₃₀ -alkyl radical. These include, for example, acrylate / beheneth-25-methacrylate copolymers, which are available under the name Aculyn ^® (Rohm + Haas). Particularly suitable polymers are also copolymers of t-butyl acrylate, ethyl acrylate, methacrylic acid (for example, Luvimer ^® 100P, Luvimer ^® Pro55) and copolymers of ethyl acrylate and methacrylic acid (for example, Luvimer ^® MAE).

Also suitable are crosslinked polymers of acrylic acid, as available under the INCI name Carbomer. Such crosslinked homopolymers of acrylic acid are commercially available for example as Carbopol ^® (Noveon). Also hydrophobically modified crosslinked polyacrylate polymers, such as Carbopol ^® Ultrez 21 (Noveon) are preferred. Such other polymers can also be used for the rheology modification of the preparations, ie as thickeners.

Also suitable as additional polymers are water-soluble or water-dispersible polyesters, polyureas, polyurethanes, polyurethaneureas, maleic anhydride copolymers optionally reacted with alcohols or anionic polysiloxanes.

Further suitable polymers for use with the polymers A are e.g. also cationic and cationogenic polymers. These include, for example

Copolymers of N-vinylpyrrolidone / N-vinylimidazolium salts (for example, available under the trade names Luviquat ^® FC, Luviquat ^® HM, Luviquat ^® MS, Luviquat ^® Care, Luviquat ^® Ultra Care (BASF),

Copolymers of N-vinylcaprolactam / N-vinylpyrrolidone / N-vinylimidazolium salts (for example, available under the trade name Lu viquat ^® Hold), Copolymers of N-vinylpyrrolidone / dimethylaminoethyl methacrylate, quaternized with diethyl sulfate Siert (for example, available under the trade name Luvi- quat ^® PQ 11),

Copolymers of vinylpyrrolidone, methacrylamide, vinylimidazole (Luviset ^® Clear) - cationic cellulose derivatives (Polyquaternium-4 and -10),

Acrylamide copolymers (Polyquaternium-7),

Guar hydroxypropyl trimethyl ammonium chloride (INCI: hydroxypropyl guar hydroxypropyl trimonium chlorides),

Polyethyleneimines and their salts, polyvinylamines and their salts,

Polymers based on dimethyldiallylammonium chloride (Merquat ^®), polymers which are formed by reaction of polyvinylpyrrolidone with quaternary ammonium compounds (Gafquat ^®),

Hydroxyethylcellulose with cationic groups (Polymer ^® JR) and - cationic polymers based on plants, for example guar polymers, such as the Jaguar brands from the company Rhodia.

As a further hair cosmetics polymers and neutral polymers are suitable as

Polyvinylpyrrolidones, copolymers of N-vinylpyrrolidone and vinyl acetate and / or vinyl propionate,

Polysiloxanes, polyvinylcaprolactams and copolymers with N-vinylpyrrolidone,

Cellulose derivatives, polyaspartic acid salts and derivatives,

Polyamides, e.g. based on itaconic acid and aliphatic diamines, as described in DE-A-43 33 238,

Among the above-mentioned types of polymers include those known under the trade name Luviskol ^® (K, VA, Plus), PVP K, PVP / VA, Advantage ^® HC, Luviflex ^® Swing, Kollicoat IR ^®, _H2 OLD EP ^® -1.

Also suitable as further polymers are biopolymers, ie polymers which are obtained from naturally renewable raw materials and are composed of natural monomer building blocks, for example cellulose derivatives, chitin, chitosan, DNA, hyaluronic acid and RNA derivatives. Suitable mixing partners for the polymers according to the invention are also zwitterionic polymers, as disclosed, for example, in German patent applications DE 39 29 973, DE 21 50 557, DE 28 17 369 and DE 37 08 451, and also methacrylic ethyl betaine / methacrylate copolymers which are disclosed in US Pat the name Amersette® ^® (A- Amerchol), are commercially available or copolymers of hydroxyethyl methacrylate, methyl methacrylate, N, N-dimethylaminoethyl methacrylate and acrylic acid (Jordapon ^®). Other suitable polymers include betainic polymers such as Yukaformer (R205, SM) and diaformer.

Suitable mixture partners suitable polymers are also nonionic, siloxane-containing, water soluble or dispersible polymers, for example, polyether siloxanes, such as Tegopren ^® (Goldschmidt) or Belsil ^® (Wacker).

Cosmetic and / or dermatologically active agents

Suitable cosmetically and / or dermatologically active agents are, for. As coloring agents, skin and hair pigmentation agents, tinting agents, tanning agents, bleach, keratin-hardening substances, antimicrobial agents, light filtering agents, repellent, hyperemic substances, keratolytic and keratoplastic substances, antidandruff, antiphlogistics, keratinizing substances, antioxidant or as Radical scavengers active substances, skin-moisturizing or moisturizing substances, moisturizing agents, anti-erythematous or anti-allergic active substances and mixtures thereof.

Preferred cosmetic care agents and active ingredients are AHA acids, fruit acids, ceramides, phytantriol, collagen, vitamins and provitamins, for example vitamin A, E and C, retinol, bisabolol and panthenol. A particularly preferred cosmetic care substance in the inventive preparations is panthenol, which is commercially available for example, as D-Panthenol USP ^®, D-Panthenol 50 P ^®, D-Panthenol 75 W ^®, D, L-Panthenol 50 W ^®.

Artificial skin tanning agents that are suitable for tanning the skin without natural or artificial irradiation with UV rays, z. Dihydroxyacetone, alloxan and walnut shell extract. Suitable keratin-hardening substances are as a rule active substances, as are also used in antiperspirants, such as, for example, Potassium aluminum sulfate, aluminum hydroxychloride, aluminum lactate, etc.

Antimicrobial agents are used to destroy microorganisms or to inhibit their growth and thus serve both as a preservative and as a deodorizing substance, which reduces the formation or intensity of body odor. These include, for example, conventional preservatives known to the person skilled in the art, such as p-hydroxybenzoic acid esters, imidazolidinyl urea, formaldehyde, sorbic acid, benzoic acid, salicylic acid, etc. Such substances having a deodorizing action are, for example, Zinc ricinoleate, triclosan, undecylenic acid alkylolamides, citric acid triethyl ester, chlorhexidine, etc. The preparations according to the invention contain preferably from 0.01 to 5, particularly preferably from 0.05 to 1,% by weight of at least one preservative. Suitable further preservatives are those listed in the International Cosmetic Ingredient Dictionary and Handbook, 9th edition with the function "Preservatives" Fabrics, eg. Phenoxyethanol, benzylparaben, butylparaben, ethylparaben, isobutylparaben, isopropylparaben, methylparaben, propylparaben, iodopropynylbutylcarbamate, methyldibromoglutaronitrile, DMDM hydantoin.

UV filters

The preparations according to the invention may in one embodiment contain oil-soluble and / or water-soluble UVA and / or UVB filters.

The total amount of the filter substances is preferably from 0.01 to 10% by weight or from 0.1 to 5% by weight, particularly preferably from 0.2 to 2% by weight, based on the total weight of the preparations.

The majority of sunscreens in the human epidermis preparations are composed of compounds which absorb UV light in the UV-B range. For example, the proportion of UV-A absorbers to be used according to the invention is from 10 to 90% by weight, preferably from 20 to 50% by weight, based on the total amount of UV-B and UV-A absorbing substances.

The UVB filters may be oil-soluble or water-soluble. Advantageous UVB filter substances are, for example: i) benzimidazole sulphonic acid derivatives, e.g. 2-phenylbenzimidazole-5-sulfonic acid and its salts; ii) benzotriazole derivatives such as e.g. 2,2'-methylene-bis- (6- (2H-benzotriazol-2-yl) -4-

(1,1,3,3-tetramethylbutyl) phenol); iii) 4-aminobenzoic acid derivatives, preferably (2- ethylhexyl) 4- (dimethylamino) benzoate, 4- (dimethylamino) benzoic acid amyl ester; iv) esters of benzalmalonic acid, preferably di (2-ethylhexyl) 4-methoxybenzalmalonate; v) esters of cinnamic acid, preferably 4-methoxycinnamic acid (2-ethylhexyl) ester, 4-

methoxycinnamate; vi) derivatives of benzophenone, preferably 2-hydroxy-4-methoxybenzophenone, 2-hydroxy-4-methoxy-4'-methylbenzophenone, 2,2'-dihydroxy-4-methoxybenzophenone; vii) methylidene camphor derivatives, preferably 4-methylbenzylidene camphor, benzylidene camphor; viii) triazine derivatives, preferably 4,4 ^l, 4 "- (1,3,5-triazine-2,4,6-triylimino) tris benzoic acid tris (2-ethylhexyl) [INCI: Diethylhexyl Butamido triazines UVA -

Sorb® HEB (Sigma 3V)] and 2,4,6-tris [anilino (p-carbo-2 ^l -ethyl-1 ^l -hexyloxy)] - l

, 3,5-triazine [INCI: Octyl Triazone, Uvinul ^® T 150 (BASF)].

Water-soluble UVB filter substances which are advantageously to be used are, for example, sulfonic acid derivatives of 3-benzylidene camphor, such as, for example, 4- (2-oxo-3-bomylidenemethyl) benzenesulfonic acid, 2-methyl-5- (2-oxo-3-bomylidenemethyl ) sulfonic acid and its salts. Advantageously to be used UVA filters are, for example:

1-phenylenedimethine camphorsulfonic acid derivatives, e.g. 3,3 '- (1,4-phenylenedimethine) bis- (7,7-dimethyl-2-oxobicyclo [2.2.1] heptane-1-methamsulfonic acid and its salts

- 1, 3,5-triazine derivatives such as 2,4-bis {[(2-ethylhexyloxy) -2-hydroxy) -phenyl} -6- (4-methoxyphenyl) -l, 3,5) -triazine (eg Tinosorb ^® S (Ciba))

- Dibenzoylmethanderivate, preferably 4-isopropyldibenzoylmethane, 4- (tert-butyl) -4'-nnethoxydibenzoylnnethan - benzoxazole derivatives, for example, the 2,4-bis [4- [5- (1, 1-dimethyl-propyl) benzoxazole -2-yl] phenylimino] -6 - [(2-ethylexyl) imino] -1, 3,5- triazine (CAS No. 288254-1 6-0, Uvasorb K2A ^® (3V Sigma).)

- Hydroxybenzophenones, for example the 2- (4'-diethylamino-2 ¹ -hydoxybenzoyl) - benzoate (also: aminobenzophenone) (Uvinul A Plus ^® (BASF))

Furthermore, according to the invention, it may be advantageous to provide preparations with further UVA and / or UVB filters, for example certain salicylic acid derivatives such as 4-isopropylbenzyl salicylate, 2-ethylhexyl salicylate, octyl salicylate, homo-menthyl salicylate. The total amount of salicylic acid derivatives in the cosmetic preparations is advantageously selected from the range of 0.1 to 15.0, preferably 0.3 to 10.0,% by weight, based on the total weight of the preparations. A further accordance with the invention to be used advantageously sunscreen is ethylhexyl-2-cyano-3,3-diphenylacrylate (octocrylene, Uvinul ^® N 539 (BASF)).

The following table provides, by way of example, a number of light protection filters suitable for use in the preparations according to the invention:

Suitable UV light protection filters with the CAS no. 113010-52-9 are commercially available for example under the name Uvinul® ^® P 25th

Polymeric or polymer-bound filter substances can also be used according to the invention.

Metal oxides such as titanium dioxide or zinc oxide can also be advantageously used to protect against harmful solar radiation. Their effect is based essentially on reflection, scattering and absorption of harmful UV radiation and depends essentially on the primary particle size of the metal oxides. The cosmetic preparations according to the invention may advantageously also comprise inorganic pigments based on metal oxides and / or other sparingly soluble or insoluble metal compounds selected from the group of the oxides of zinc (ZnO), iron (eg Fe ₂ O ₃ ), zirconium (ZrO ₂ ) , Silicon (SiO ₂ ), manganese (eg MnO), aluminum (Al ₂ O ₃ ), cerium (eg Ce ₂ O ₃ ), mixed oxides of the corresponding metals and mixtures of such oxides. Particular preference is given to pigments based on ZnO.

The inorganic pigments may be present in coated form, i. that they are superficially treated. This surface treatment can be, for example, that the pigments are provided in a manner known per se, as described in DE-A-33 14 742, with a thin hydrophobic layer.

Suitable sunscreens for use in the preparations according to the invention are the compounds mentioned in EP-A 1 084 696 in paragraphs [0036] to [0053], to which reference is made in full at this point. Suitable for use according to the invention are all UV photoprotective filters, which are mentioned in Appendix 7 (to § 3b) of the German Cosmetics Regulation under "Ultraviolet filters for cosmetic products".

The list of said UV light protection filters which can be used in the preparations according to the invention is not exhaustive.

thickener

Suitable thickening agents are mentioned in "Cosmetics and hygiene from head to toe", ed. W. Umbach, 3rd edition, Wiley-VCH, 2004, pages 235-236, to which reference is made at this point in their entirety.

Consistency regulators make it possible to adjust the desired viscosity of, for example, shampoos. Thickeners, which increase the viscosity of surfactant micelles or swell the water phase, have chemically very different classes of substances.

Suitable thickeners for the preparations according to the invention are, for example, crosslinked polyacrylic acids and their derivatives, polysaccharides such as Xanthan gum, guar guar, agar, alginates or tyloses, cellulose derivatives, e.g. As carboxymethylcellulose or hydroxycarboxymethylcellulose, also higher molecular weight polyethylene glycol mono- and diesters of fatty acids, fatty alcohols, monoglycerides and fatty acids, polyvinyl alcohol and polyvinylpyrrolidone. Suitable thickeners are available commercially under the trade name Carbopol ^® (Noveon), Ultrez ^® (Noveon), Luvigel ^® EM (BASF), Capigel ^® 98 (Seppic), Synthalens ^® (Sigma), Aculyn ^® (Rohm and Haas) as Aculyn ^® 22 (copolymer of acrylates and methacrylic acid with stearyl (20 EO units)) and Aculyn ^® 28 (copolymer of acrylates and Methacrylsäureethoxilaten with behenyl (25 EO units)).

Further suitable thickeners are, for example, Aerosil types (hydrophilic silicic acids), polyacrylamides, polyvinyl alcohol and polyvinylpyrrolidone, surfactants such as ethoxylated fatty acid glycerides, esters of fatty acids with polyols such as pentaerythritol or trimethylolpropane, fatty alcohol ethoxylates with restricted homolog distribution or alkyl oligoglucosides and electrolytes such as common salt and ammonium chloride ,

Particularly preferred thickening agents for the preparation of gels are ^® Ultrez 21, Aculyn ^® 28, Luvigel EM ^® and Capigel ^® 98th

In particular in the case of more highly concentrated shampoo formulations, substances which reduce the viscosity of the formulation, such as, for example, can be added to regulate the consistency. As propylene glycol or glycerol. These substances have little influence on the product properties.

Gelling agent If the use of gelling agents is desired for the preparations according to the invention, then it is possible to use all gel formers customary in cosmetics. These include slightly crosslinked polyacrylic acid, for example carbomer (INCI), cellulose derivatives, eg hydroxypropylcellulose, hydroxyethylcellulose, cationically modified celluloses, polysaccharides, eg xanthum gum, caprylic / capric triglycerides, sodium acrylate copolymer, polyquaternium-32 (and) paraffin liquidum (INCI ), Sodium Acrylates Copolymer (and) Paraffin Liquidum (and) PPG-1 Trideceth-6, Acrylamidopropyl Trimonium Chloride / Acrylamide Copolymer, Steareth-1 O Allyl Ether Acrylate Copolymer, Polyquaternium-37 (and) Paraffin Liquidum (and) PPG -1 Trideceth-6, Polyquaternium 37 (and) Propylene Glycols Dicaprate Dicaprylate (and) PPG-1 Trideceth-6, Polyquaternium-7, Polyquaternium-44. emulsifiers

Suitable emulsifiers are, for example, nonionic surfactants from at least one of the following groups: addition products of from 2 to 30 moles of ethylene oxide and / or from 0 to 5 moles of propylene oxide onto linear fatty alcohols containing from 8 to 22 carbon atoms, to fatty acids containing from 12 to 22 carbon atoms Atoms and alkylphenols having 8 to 15 carbon atoms in the alkyl group; o C12 / 18 fatty acid mono- and diesters of addition products of 1 to 30 moles of ethylene oxide with glycerol; o Glycerol mono- and diesters and sorbitan mono- and diesters of saturated and unsaturated fatty acids having 6 to 22 carbon atoms and their ethylene oxide addition products; o alkyl mono- and oligoglycosides having 8 to 22 carbon atoms in the alkyl radical and their ethoxylated analogs; o addition products of 15 to 60 moles of ethylene oxide with castor oil and / or hydrogenated castor oil; Polyol and in particular polyglycerol esters, such as, for example, polyglycerol polyricinoleate, polyglycerol poly-12-hydroxy stearate or polyglycerol dimerate. Also suitable are mixtures of compounds of several of these classes of substances; o addition products of 2 to 15 moles of ethylene oxide with castor oil and / or hydrogenated castor oil; o partial esters based on linear, branched, unsaturated or saturated C _6/22 fatty acids, ricinoleic acid and 12-hydroxystearic acid and glycerol, polyglycerol, pentaerythritol, dipentaerythritol, sugar alcohols

(eg sorbitol), alkylglucosides (eg methylglucoside, butylglucoside, laurylglucoside) as well as polyglucosides (eg cellulose); o mono-, di- and trialkyl phosphates and mono-, di- and / or tri-PEG-alkyl phosphates and their salts; o wool wax alcohols; o polysiloxane-polyalkyl-polyether copolymers or corresponding derivatives; Mixed esters of pentaerythritol, fatty acids, citric acid and fatty alcohol according to DE-PS 1165574 and / or mixed esters of fatty acids having 6 to 22 carbon atoms, methylglycose and polyols, preferably glycerol or polyglycerol and o polyalkylene glycols.

The addition products of ethylene oxide and / or of propylene oxide to fatty alcohols, fatty acids, alkylphenols, glycerol mono- and diesters and sorbitan mono- and diesters of fatty acids or castor oil are known, commercially available products. These are homolog mixtures whose mean Al koxylie- degree of the ratio of the amounts of ethylene oxide and / or propylene oxide and substrate, with which the addition reaction is carried out corresponds. C ₂ to C ₈ fatty acid monoesters and diesters of addition products of ethylene oxide onto glycerol rin are known from DE-PS 2024051 as refatting agents for cosmetic preparations. C ₈ to C ₈ alkyl mono- and oligoglycosides, their preparation and their use are known from the prior art. They are prepared in particular by reacting glucose or oligosaccharides with primary alcohols having 8 to 18 carbon atoms. With respect to the glycoside ester, it is true that both monoglycosides in which a cyclic sugar residue is glycosidically linked to the fatty alcohol and oligomeric glycosides having a degree of oligomerization of preferably about 8 are suitable. The degree of oligomerization is a statistical mean, which is based on a homolog distribution typical for such technical products.

Furthermore, zwitterionic surfactants can be used as emulsifiers. Zwitterionic surfactants are surface-active compounds which carry at least one quaternary ammonium group and at least one carboxylate and / or one sulfonate group in the molecule. Particularly suitable zwitterionic surfactants are the so-called betaines, such as the N-alkyl-N, N-dimethylammonium glycinates, for example the Kokosalkyldimethylammoniumglyci- nat, N-acylaminopropyl-N, N-dimethylammoniumglycinate, for example, the Kokosa- cylaminopropyldimethylammoniumglycinat, and 2-alkyl-3-carboxylmethyl -3- hydroxyethylimidazolines having in each case 8 to 18 carbon atoms in the alkyl or acyl group and Kokosacylaminoethylhydroxyethylcarboxy methylglycinat.

Particularly preferred is the fatty acid amide derivative known under the CTFA name Cocamidopropyl Betaine. Also suitable emulsifiers are ampholytic surfactants. Ampholytic surfactants are surface-active compounds which, in addition to a C to C alkyl- _{8 8} -alkyl or -acyl group in the molecule contain at least one free amino group and at least one -COOH and / or -SO ₃ H group and to form internal Salts are capable. Examples of suitable ampholytic surfactants are N-alkylglycines, N-alkylpropionic acids, N-

Alkylaminobutyric, N-Alkyliminodipropionsäuren, N-hydroxyethyl-N-alkylamidopropylglycines, N-alkyltaurines, N-alkylsarcosines, 2-Alkylaminopropionsäuren and Alkylaminoessigsäuren each having about 8 to 18 carbon atoms in the alkyl group. Particularly preferred ampholytic surfactants are N-cocoalkylaminopropionate, cocoacylaminoethyl aminopropionate and C ₂ to C ₈ acyl sarcosine. In addition to the ampholytic, quaternary emulsifiers are also suitable, with those of the esterquat type, preferably methyl-quaternized difatty acid triethanolamine ester salts, being particularly preferred.

antioxidants

An additional content of the antioxidant preparations may be advantageous. According to the invention, all antioxidants suitable or used for cosmetic applications can be used as antioxidants. Advantageously, the antioxidants are selected from the group consisting of amino acids (eg glycine, histidine, tyrosine, tryptophan) and their derivatives, imidazoles (eg urocanic acid) and their derivatives, peptides such as D, L-camosine, D-camosine, L-camosine and their derivatives (eg anserine), carotenoids, carotenes (eg α-carotene, β-carotene, γ-lycopene) and their derivatives, chlorogenic acid and its derivatives, lipoic acid and its derivatives (eg dihydrolipoic acid), aurothioglucose, propylthiouracil and other thiols (eg Thioredoxin, glutathione, cysteine, cystine, cystamine and their glycosyl, N-acetyl, methyl, ethyl, propyl, amyl, butyl and lauryl, palmitoyl, oleyl, γ-linoleyl, chlorine lesteryl and glyceryl esters) and their salts, dilaurylthiodipropionate, distearylthiodipropionate, thiodipropionic acid and derivatives thereof (esters, ethers, peptides, lipids, nucleotides, nucleosides and salts) and sulfoximine compounds (eg buthionine sulfoximines, homocysteinsulfoximine, buthione sulfo ne, penta, hexa, heptathionine sulfoxi- min) in very low tolerated dosages (eg pmol to μmol / kg), furthermore (metal) chelators (eg α-hydroxyfatty acids, palmitic acid, phytic acid, lactoferrin), α-hydroxy acids (z. Citric acid, lactic acid, malic acid), humic acid, bile acid, bile extracts, bilirubin, biliverdin, EDTA, EGTA and their derivatives, unsaturated fatty acids and their derivatives (eg γ-linolenic acid, linoleic acid, oleic acid), folic acid and its derivatives, furfurylidene sorbitol and its derivatives Derivatives, ubiquinone and ubiquinol and their derivatives, vitamin C and derivatives (eg ascorbyl palmitate, Mg ascorbyl phosphate, ascorbyl acetate), tocopherols and derivatives (eg vitamin E acetate), vitamin A and derivatives (vitamin A palmitate) and coniferyl benzoate of Benzoin, rutinic acid and derivatives thereof, α-glycosyl rutin, ferulic acid, furfurylidenglucitol, carnosine, butylhydroxytoluene, butylhydroxyanisole, nordihydroguaiacetic acid, nordihydroguaiaretic acid, trihydroxybutyrophenone, uric acid and its derivatives, mannose and its derivatives, zinc and its derivatives (eg ZnO , ZnSO ₄ ) selenium and its derivatives (eg selenium methionine), stilbenes and their derivatives (eg stilbene oxide, trans-style benoxi d) and the inventively suitable derivatives (salts, esters, ethers, sugars, nucleotides, nucleosides, peptides and lipids) of these active substances.

The amount of the aforementioned antioxidants (one or more compounds) in the preparations is preferably 0.001 to 30 wt .-%, particularly preferably 0.05 to 20 wt .-%, in particular 0.1 to 10 wt .-%, based on the total weight of

Preparation.

If vitamin E and / or its derivatives are the antioxidant (s), it is advantageous to use them in concentrations of 0.001 to 10% by weight, based on the

Total weight of the preparation to provide.

If vitamin A, or vitamin A derivatives, or carotenes or derivatives thereof are the antioxidant or antioxidants, it is advantageous to provide them in concentrations of from 0.001 to 10% by weight, based on the total weight of the preparation.

perfume oils

The cosmetic, preferably hair cosmetic preparations may contain perfume oils. As perfume oils, for example, mixtures of natural and synthetic fragrances may be mentioned. Natural fragrances are extracts of flowers (lily, lavender, rose, jasmine, neroli, ylang-ylang), stems and leaves (geranium, patchuli, petitgrain), fruits (anise, coriander, caraway, juniper), fruit peel

(Bergamot, lemon, orange), roots (macis, angelica, celery, cardamom, costus, iris, calmus), woods (pine, sandal, guaiac, cedar, rosewood), herbs and grasses (tarragon, lemongrass, Sage, thyme), needles and twigs (spruce, fir, pine, pines), resins and balsams (galbanum, elemi, benzoin, myrrh, olibanum, opoponax). Furthermore, animal raw materials come into question, such as civet and Castoreum. Typical synthetic fragrance compounds are ester type products, ethers, aldehydes, ketones, alcohols and hydrocarbons. Fragrance compounds of the ester type are, for example, benzyl acetate, phenoxyethyl isobutyrate, 4-tert-butylcyclohexyl acetate, linalyl acetate, dimethylbenzylcarbinyl acetate, phenylethyl acetate, linalyl benzoate, benzylformate, ethylmethylphenylglycinate, allylcyclohexylpropionate, styrallylpropionate and benzylsalicylate. The ethers include, for example, benzyl ethyl ether, to the aldehydes, for example, the linear alkanals having 8 to 18 carbon atoms, citral, citronellal, citronellyloxyacetaldehyde, cyclamen aldehyde, hydroxycitronel IaI, lilial and bourgeonate, to the ketones such as the ionones, cc-lsomethylionen and Me - Thylcedrylketon to the alcohols anethof, citronellol, eugenol, isoeugenol, geraniol, linalool, phenylethyl alcohol and terioneol, the hydrocarbons include mainly the terpenes and balsams. Preferably, however, mixtures of different fragrances are used, which together produce an attractive fragrance. Essential oils of lower volatility, which are usually used as aroma components, are suitable as perfume oils, for example sage oil, chamomile oil, clove oil, oil, mint oil, cinnamon oil, lime blossom oil, juniper berry oil, vetiver oil, oliban oil, galbanum oil, labolanum oil and lavandin oil. Preferably, bergamot oil, dihydromyrcenol, lilial, lyral, citronellol, phenylethyl alcohol, a-hexylcinnamaldehyde, geraniol, benzylacetone, cyclamen aldehyde, linalool, Boisambrene Forte, Ambroxan, indole, hedione, sandelice, citron oil, tangerine oil, orange oil, allylamyl glycolate, cyclohexane tallow, lavandin oil, muscat sage oil, β-damascone, geranium oil bourbon, cyclohexyl salicylate, Vertofix Coeur, Iso-E-Super, fixolide NP, evernyl, iraldeine gamma, phenylacetic acid, geranyl acetate, benzyl acetate, rose oxide, romillate, irotyl and floramate used alone or in mixtures.

superfatting

Superfatting agents which can be used are substances such as lanolin and lecithin, as well as polyethoxylated or acylated lanolin and lecithin derivatives, polyol fatty acid esters, monoglycerides and fatty acid alkanolamides, the latter also serving as foam stabilizers.

silicone compounds

In one embodiment, the preparations according to the invention contain as hair-care additive at least one silicone compound in an amount of preferably 0.01 to 15 wt.%, Particularly preferably from 0.1 to 5 wt.%. The silicone compounds include volatile and non-volatile silicones and agent-soluble and insoluble silicones. In one embodiment, it is high molecular weight silicones having a viscosity of 1,000 to 2,000,000 cSt at 25 ° C, preferably 10,000 to 1,800,000 or 100,000 to 1,500,000. The silicone compounds include polyalkyl and polyaryl siloxanes, especially with methyl, ethyl, propyl, phenyl, methylphenyl and phenylmethyl groups. Preference is given to polydimethylsiloxanes, polyethylsiloxanes, polymethylphenylsiloxanes. Shiny, arylated silicones with a refractive index of at least 1.46, or at least 1. 52 are also preferred. The silicone compounds include, in particular, the substances with the INCI names cyclomethicone, dimethicone, dimethiconol, dimethicone copolyol, phenyl trimethicone, amodimethicone, trimethylsilylamodimethicone, stearyl siloxysilicate, polymethylsilsesquioxane, dimethicone crosspolymer. Also suitable are silicone resins and silicone elastomers, which are highly crosslinked siloxanes.

Preferred silicones are cyclic dimethylsiloxanes, linear polydimethylsiloxanes, block polymers of polydimethylsiloxane and polyethylene oxide and / or polypropylene oxide, polydimethylsiloxanes having terminal or pendant polyethylene oxide or polypropylene oxide radicals, hydroxyl-terminated polydimethylsiloxanes, phenyl-substituted polydimethylsiloxanes, silicone emulsions, silicone elastomers, silicone waxes, silicone gums and amino-substituted silicones (CTFA: amodimethicone).

hair conditioners

In one embodiment, the preparations according to the invention contain from 0.01 to 20, preferably from 0.05 to 10, particularly preferably from 0.1 to 5,% by weight of at least one conditioning agent. Conditioning agents which are preferred according to the invention are, for example, all compounds which are described in the International Cosmetic Ingredient Dictionary and Handbook (Volume 4, editors: RC Pepe, JA Wenninger, GN McEwen, The Cosmetic, Dental and Fragrance Association, 9th edition, 2002) under Section 4 are listed under the headings Hair Conditioning Agents, Humectants, Skin Conditioning Agents, Skin Conditioning Agents Emollient, Skin Conditioning Agents Humectant, Skin- Conditioning Agents-Miscellaneous, Skin Conditioning Agents-Occlusive and Skin Protectants, and others all compounds listed in EP-A 934 956 (S.11-13) under "water-soluble conditioning agent" and "oil-soluble conditioning agent". Further advantageous conditioning agents are, for example, the compounds designated as polyquaternium according to INCI ( in particular Polyquaternium-1 to Polyquaternium-56).

Suitable conditioning agents include, for example, polymeric quaternary ammonium compounds, cationic cellulose derivatives, chitosan derivatives and polysaccharides.

The conditioning agent is preferably selected from betaine, panthenol, panthenyl ether, sorbitol, protein hydrolysates, plant extracts; A-B block copolymers of alkyl acrylates and alkyl methacrylates; A-B block copolymers of alkyl methacrylates and acrylonitrile; A-B-A block copolymers of lactide and ethylene oxide; A-B-A block copolymers of caprolactone and ethylene oxide; A-B-C block copolymers of alkylene or alkadiene compounds, styrene and alkyl methacrylates; A-B-C block copolymers of acrylic acid, styrene and alkyl methacrylates, star-shaped block copolymers, hyperbranched polymers, dendrimers, intrinsically electrically conductive 3,4-polyethylenedioxythiophenes and intrinsically electrically conductive polyanilines.

Further inventively advantageous conditioning agents represent cellulose derivatives and quaternized guar gum derivatives, in particular guar hydroxypropylammonium (eg Jaguar Excel ^®, Jaguar C 162 ^® (Rhodia), CAS 65497-29-2, CAS 39421-75-5).

And nonionic poly-N-vinylpyrrolidone / polyvinyl acetate copolymers (eg Lu viskol ^® VA 64 (BASF)), anionic acrylate copolymers (eg Luviflex Soft ^® (BASF)), and / or amphoteric amide / acrylate / methacrylate copolymers (for example Amphomer.RTM ^® (National Starch)) can be used advantageously according to the invention as conditioners.

Hydrotropes In order to improve the flow behavior, it is also possible to use hydrotropes, such as, for example, ethanol, isopropyl alcohol, or polyols. Polyols contemplated herein preferably have from 2 to 15 carbon atoms and at least two hydroxyl groups. Typical examples are

glycerol; Alkylene glycols such as ethylene glycol, diethylene glycol, propylene glycol, butylene glycol, hexylene glycol, and polyethylene glycols having an average molecular weight of 100 to 1000 daltons; technical oligoglycerine mixtures having an intrinsic degree of condensation of 1.5 to 10, such as technical grade diglycerin mixtures having a diglycerol content of

40 to 50% by weight;

Methylol compounds, in particular trimethylolethane, trimethylolpropane, trimethylolbutane, pentaerythritol and dipentaerythritol;

Niedrigalkylglucoside, in particular those having 1 to 8 carbons in the alkyl radical, such as methyl and Butylglucosid;

Sugar alcohols having 5 to 12 carbon atoms, such as sorbitol or mannitol;

Sugars having 5 to 12 carbon atoms, such as glucose or sucrose; - Aminosugars, such as glucamine.

oils, fats and waxes

The cosmetic, preferably hair cosmetic preparations according to the invention may also contain oils, fats or waxes. Such is advantageously selected from the group of lecithins and fatty acid triglycerides, namely the triglycerol esters of saturated and / or unsaturated, branched and / or unbranched alkanecarboxylic acids having a chain length of 8 to 24, in particular 12 to 18, carbon atoms. The fatty acid triglycerides can be selected, for example, advantageously from the group of synthetic, semisynthetic and natural oils, such as olive oil, sunflower oil, soybean oil, peanut oil, rapeseed oil, almond oil, palm oil, coconut oil, castor oil, wheat germ oil, grape seed oil, thistle oil, evening primrose oil, macadamia nut oil and such more. Other polar oil components can be selected from the group of esters of saturated and / or unsaturated, branched and / or unbranched alkanecarboxylic acids having a chain length of 3 to 30 carbon atoms and saturated and / or unsaturated, branched and / or unbranched alcohols a chain length of 3 to 30 carbon atoms and from the group of esters of aromatic carboxylic acids and saturated and / or unsaturated, branched and / or unbranched alcohols having a chain length of 3 to 30 carbon atoms. Such ester oils can then advantageously be selected from the group isopropyl myristate, isopropyl palmitate, isopropyl stearate, isopropyl ether, n-butyl stearate, n-hexyl laurate, n-decyl oleate, isooctyl stearate, isononyl stearate, isononyl isononanoate, 2-ethylhexyl palmitate, 2-ethylhexyl laurate, 2-hexyldecyl stearate, 2-octyl dodecyl palmitate, oleyl oleate, oleyl erucate, erucyl oleate, erucyl erucate dicaprylyl carbonate (Cetiol CC) and cocoglycerides (Myritol 331), butylene glycol dicaprylate / dicaprate and dibutyl adipate as well as synthetic, semi-synthetic and natural mixtures of such esters, such as jojoba oil.

Furthermore, one or more olefin components can advantageously be selected from the group of branched and unbranched hydrocarbons and waxes, the SiI-konöle, the dialkyl ethers, the group of saturated or unsaturated, branched or unbranched alcohols.

Any mixtures of such oil and wax components are also advantageous to use in the context of the present invention. It may also be advantageous, if appropriate, to use waxes, for example cetyl palmitate, as the sole lipid component of the oil phase.

According to the invention, the olefin component is advantageously selected from the group consisting of 2-ethylhexyl isostearate, octyldodecanol, isotridecyl isononanoate, isoeicosane, 2-ethylhexyl cocoate, C12-15-alkyl benzoate, caprylic capric acid triglyceride, dicaprylyl ether. Advantageous according to the invention are mixtures of C 12-15 -alkyl benzoate and 2-

Ethylhexyl isostearate, mixtures of C12-15 alkyl benzoate and isotridecyl isononanoate and mixtures of C12-15 alkyl benzoate, 2-ethylhexyl isostearate and isotridecyl isononanoate. Particular preference according to the invention is given to using fatty acid triglycerides, in particular soybean oil and / or almond oil, as oils having a polarity of from 5 to 50 mN / m.

Furthermore, the oil phase can advantageously be selected from the group of Guerbet alcohols. These are liquid even at low temperatures and cause practically no skin irritation. Advantageously, they can be used as greasing, overfatting and also moisturizing ingredients in cosmetic compositions. The use of Guerbet alcohols in cosmetics is known per se.

According to the invention preferred Guerbet alcohols are (commercially available, for example as lsofol ^® 12 (Condea)) 2-butyloctanol and 2-hexyl decanol (for example commercially available as iso- fol ^® 16 (Condea)). Mixtures of Guerbet alcohols according to the invention are also advantageously usable according to the invention, for example mixtures of 2-butyloctanol and 2-hexyldecanol (commercially available, for example, as Isofol 14 (Condea)). Any mixtures of such oil and wax components are also advantageous to use in the context of the present invention. Among the polyolefins, polydecenes are the preferred substances. Fat and / or wax components which can advantageously be used according to the invention can be selected from the group of vegetable waxes, animal waxes, mineral waxes and petrochemical waxes. Candelilla wax, carnauba wax, Japan wax, Esparto grass wax, cork wax, guaruma wax, rice germ oil wax, sugarcane wax, berry wax, ouricury wax, montan wax, jojoba wax, shea butter, beeswax, shellac wax, spermaceti, lanolin (wool wax), crepe wax, ceresin are advantageous, for example , Ozokerite (ground wax), paraffin waxes and micro-waxes. Further advantageous fat and / or wax components are chemically modified waxes and synthetic waxes such as Syncrowax ^® (glyceryl tribehenate), and Syncrowax ^® AW 1 C (C _8-36 fatty acid) as well as Montanesterwachse, sasol, hydrogenated jojoba , synthetic or modified beeswaxes (z. B. dimethicone copolyol beeswax and / or C _3O-5 -alkyl beeswax), cetyl ricinoleates leate such as Tegosoft ^® CR, polyalkylene waxes, polyethylene glycol waxes, but also chemically modified fats such. Hydrogenated vegetable oils (for example hydrogenated castor oil and / or hydrogenated coconut fat glycerides), triglycerides such as hydrogenated soy glyceride, trihydroxystearin, fatty acids, fatty acid esters and glycol kolester such as C ₂ o- ₄ o-alkyl stearate, C ₂ o- ₄ o-Alkylhydroxystearoylstearat and / or glycol montanate. Other advantageous compounds are certain organosilicon compounds which have similar physical properties to the abovementioned fatty and / or wax components, for example stearoxytrimethylsilane. According to the invention, the fat and / or wax components can be used both individually and as a mixture in the compositions.

Any mixtures of such oil and wax components are also advantageous to use in the context of the present invention.

The oil phase is selected from the group 2-ethylhexyl advantageous Octyldo- decanol, isotridecyl isononanoate, butylene glycol dicaprylate / dicaprate, 2-ethylhexyl cocoate, C _2- i ₅ alkyl benzoate, caprylic-capric acid triglyceride, dicaprylyl ether. Particularly advantageous are mixtures of octyldodecanol, caprylic-capric acid triglyceride, dicaprylyl ether, dicaprylyl carbonate, cocoglycerides, or mixtures of C _2-15 alkyl benzoate and 2-ethylhexyl isostearate, mixtures of C ₂ i ₅ alkyl benzoate and butylene glycol dicaprylate / dicaprate and mixtures from Ci _2- i ₅ alkyl benzoate, 2-ethylhexyl isostearate and Isotridecylisononanoat.

Of the hydrocarbons, paraffin oil, cycloparaffin, squalane, squalene, hydrogenated polyisobutene or polydecene are to be used advantageously in the context of the present invention. The oil component is also advantageously selected from the group of phospholipids. As according to the invention advantageous paraffin oil according to the invention can Mercury ^® Weissoel Pharma 40 from Merkur Vaseline, Shell Ondina ^® 917, Shell Ondina ^® 927, Shell Oil 4222, Shell Ondina ^® 933 from Shell & DEA OiI, Pioneer ^® 6301 S, Pioneer ^® 2071 (Hansen & Rosenthal) can be used.

Suitable cosmetically acceptable oil and fat components are described in Karl-Heinz Schrader, Grundlagen und Rezepturen der Kosmetika, 2nd edition, Verlag Hüthig, Heidelberg, pp. 319-355, to which reference is hereby made in its entirety.

The content of oils, fats and waxes is at most 30, preferably 20, more preferably at most 10% by weight, based on the total weight of the composition. pigments

In one embodiment, the preparations according to the invention contain at least one pigment. These may be colored pigments which give color effects to the product mass or the hair or they may be glossy effect pigments which give the product mass or the hair gloss effects. The color or gloss effects on the hair are preferably temporary, i. they remain on the hair until the next hair wash and can be removed by washing the hair with regular shampoos.

The pigments are present in undissolved form in the product composition and may be present in an amount of from 0.01 to 25% by weight, particularly preferably from 5 to 15% by weight. The preferred particle size is 1 to 200 .mu.m, in particular 3 to 150 .mu.m, particularly preferably 10 to 100 .mu.m. The pigments are practically insoluble colorants in the application medium and may be inorganic or organic. Also inorganic-organic mixed pigments are possible. Preference is given to inorganic pigments. The advantage of inorganic pigments is their excellent light, weather and temperature resistance. The inorganic pigments may be of natural origin, for example made of chalk, ocher, umber, green soil, terraced terraza or graphite. The pigments may be white pigments, e.g. Titanium dioxide or zinc oxide to form black pigments, e.g. Iron oxide black, colored pigments such as e.g. Ultramarine or iron oxide red, to luster pigments, metallic effect pigments, pearlescent pigments, as well as fluorescent or Phosphoreszenzpigmente, preferably wherein at least one pigment is a colored, non-white pigment.

Suitable are metal oxides, hydroxides and oxide hydrates, mixed phase pigments, sulfur-containing silicates, metal sulfides, complex metal cyanides, metal sulfates,

Chromates and molybdate as well as the metals themselves (bronze pigments). Titanium dioxide (Cl 77891), black iron oxide (Cl 77499), yellow iron oxide (Cl 77492), red and brown iron oxide (Cl 77491), manganese violet (Cl 77742), ultramarines (sodium aluminum sulfosilicates, Cl 77007, Pigment Blue 29 ), Chromium oxide hydrate (C177289), iron blue (Ferric Ferro-Cyanide, CI7751 0), Carmine (Cochineal).

Particular preference is given to pearlescent and color pigments based on mica or mica which are coated with a metal oxide or a metal oxychloride, such as titanium dioxide or bismuth chloride, and optionally other coloring substances, such as iron oxides, iron blue, ultramarines, carmines, etc. tion of the layer thickness can be determined. Such pigments are marketed under the trade names Rona ^®, Colorona® ^{®, ®} and Dichrona® Timiron ^® from Merck, Germany.

Organic pigments include, for example, the natural pigments sepia, cambogia, bone charcoal, Kasseler brown, indigo, chlorophyll and other plant pigments. Synthetic organic pigments are, for example, azo pigments, anthraquinoids, Indigoids, dioxazine, quinacridone, phthalocyanine, isoindolinone, perylene and perinone, metal complex, alkali blue and diketopyrrolopyrrole pigments.

In one embodiment, the preparations according to the invention contain from 0.01 to 10, particularly preferably from 0.05 to 5,% by weight of at least one particulate substance. Suitable substances are e.g. Substances which are solid at room temperature (25 ° C) and in the form of particles. Suitable examples are silica, silicates, aluminates, clays, mica, salts, in particular inorganic metal salts, metal oxides, e.g. Titanium dioxide, minerals and polymer particles.

The particles are present in the agent undissolved, preferably stably dispersed form and can be deposited in solid form after application to the application surface and evaporation of the solvent.

Preferred particulates are silica (silica gel, silica) and metal salts, especially inorganic metal salts, with silica being particularly preferred. Metal salts are e.g. Alkali or alkaline earth halides such as sodium chloride or potassium chloride; Alkali or alkaline earth sulfates such as sodium sulfate or magnesium sulfate.

Suitable repellent agents are compounds capable of preventing or repelling certain animals, particularly insects, from humans. This includes z. B. 2-ethyl-1, 3-hexanediol, N, N-diethyl-m-toluamide, etc.

Suitable hyperemic substances which stimulate the perfusion of the skin are, for. Essential oils such as mountain pine, lavender, rosemary, juniper berry, horse chestnut extract, birch leaf extract, hay flower extract, ethyl acetate, camphor, menthol, peppermint oil, rosemary extract, eucalyptus oil, etc.

Suitable keratolytic and keratoplastic substances are for. As salicylic acid, calcium thioglycolate, thioglycolic acid and its salts, sulfur, etc. Suitable anti-dandruff agents are, for. Sulfur, polyethylene glycol sorbitan monooleate, sulfuricinol polyethoxylate, zinc pyrithione, aluminum pyrithione, etc.

Suitable anti-inflammatory drugs that counteract skin irritation, z. Allantoin, bisabolol, dragosantol, chamomile extract, panthenol, etc.

Dosage Form

The preparations according to the invention can be sprayed in a preferred embodiment, for example as an aerosol or pump spray preparation.

The preparations according to the invention can be used in various forms, for example as lotion, as non-aerosol spray lotion, which is used by means of a mechanical device for spraying, as aerosol spray which is sprayed by means of a blowing agent, as aerosol foam or as non Aerosol foam, which in combination with a suitable mechanical Device for foaming the composition is present, as a hair cream, as a hair wax, as a gel, as a liquid gel, as a sprayable gel or as a foam gel.

A use in the form of a thickened with a conventional thickener lotion is possible. In one embodiment, the agent according to the invention is in the form of a gel, in the form of a viscous lotion or in the form of a spray gel, which is sprayed with a mechanical device, and contains at least one of the abovementioned thickening agents in an amount of preferably 0.05 to 10 , particularly preferably from 0.1 to 2 wt.% And has a viscosity of at least 250 mPas. The viscosity of the gel is preferably from 500 to 50,000 mPas, more preferably from 1,000 to 15,000 mPas at 25 ° C.

In another embodiment, the preparation according to the invention is in the form of an O / W emulsion, a W / O emulsion or a microemulsion and contains at least one of the abovementioned oils or waxes emulsified in water and at least one cosmetically customary surfactant.

In a preferred embodiment, the preparation according to the invention is in the form of a spray product, either in combination with a mechanical pump spray device or in combination with at least one of the aforementioned blowing agents. A preferred aerosol spray additionally contains propellant in such an amount that the total amount of the volatile organic components does not exceed 80, in particular 55% by weight of the preparation and is filled in a pressure vessel.

A non-aerosol hair spray is sprayed by means of a suitable mechanically operated spray device. Mechanical spraying devices are to be understood as meaning devices which enable the spraying of a composition without the use of a propellant. As a suitable mechanical spraying device, for example, a spray pump or provided with a spray valve elastic container in which the cosmetic preparation of the invention is filled under pressure, wherein the elastic container expands and from the means due to the contraction of the elastic container when the spray valve is opened continuously is used.

In a further embodiment, the preparation according to the invention is in the form of a foamable product (mousse) in combination with a device for foaming, contains at least one customary foaming substance known for this purpose, for example at least one foam-forming surfactant or at least one foam-forming polymer. Foaming devices are to be understood as meaning devices which enable the foaming of a liquid with or without the use of a blowing agent. As a suitable mechanical foaming device, for example, a commercially available pump foamer or an aerosol Foam head can be used. The product is either in combination with a mechanical Pumpschäumvorrichtung (pump foam) or in combination with at least one propellant (aerosol foam) in an amount of preferably 1 to 20, in particular from 2 to 10 wt.%, Before. Propellants are, for example, selected from propane, butane, dimethyl ether and fluorinated hydrocarbons.

An object of the invention is thus a cosmetic, preferably hair cosmetic preparation in the form of a spray product, wherein the preparation either in combination with a mechanical Pumpsprühvorrichtung or in combination with at least one blowing agent selected from the group consisting of propane, butane, dimethyl ether, fluorinated hydrocarbons and mixtures thereof.

The agent is foamed immediately before use and incorporated as a foam in the hair and can then be rinsed or left without rinsing in the hair.

A preferred formulation for aerosol hair foams according to the invention contains i) from 0.1 to 10% by weight of at least one polymer A, ii) from 55 to 99.8% by weight of water and alcohol, iii) from 5 to 20% by weight of a blowing agent, iv) 0.1 to 5 wt .-% of an emulsifier, v) 0 to 10 wt .-% further constituents, wherein the total amount of VOC is at most 80 and preferably 55 wt .-%.

As emulsifiers all emulsifiers commonly used in hair foams can be used. Suitable emulsifiers may be nonionic, cationic or anionic or amphoteric. Examples of nonionic emulsifiers (INCI nomenclature) are Laurethe, z. B. Laureth-4; Cetethe, z. Cetheth-1, polyethylene glycol cetyl ether; Cetearethe, z. Cethethreeth-25, polyglycol fatty acid glycerides, hydroxylated lecithin, lactyl esters of fatty acids, alkylpolyglycosides.

Examples of cationic emulsifiers are cetyldimethyl-2-hydroxyethylammonium dihydrogenphosphate, cetyltrimonium chloride, cetyltrimmonium bromide, cocotrimonium methylsulfate, quaternium-1 to x (INCI).

Anionic emulsifiers may, for example, be selected from the group of alkyl sulfates, alkyl ether sulfates, alkyl sulfonates, alkylarlylsulfonates, alkyl succinates, alkylsulfosuccinates, N-alkoylsarcosinates, acyltaurates, acylisothionates, alkylphosphates, alkyletherphosphates, alkylethercarboxylates, alpha-olefinsulphonates, especially the alkali and alkaline earth metal salts, e.g. As sodium, potassium, magnesium, calcium, and ammonium and triethanolamine salts. The alkyl ether sulfates, alkyl ether phosphates and Alkyl ether carboxylates can have between 1 to 10 ethylene oxide or propylene oxide units, preferably 1 to 3 ethylene oxide units in the molecule.

A preparation suitable for styling gels according to the invention can be composed, for example, as follows: i) 0.1 to 10% by weight of polymer A, ii) 80 to 99.85% by weight of water and alcohol, iii) 0 to 3% by weight .-%, preferably 0.05 to 2 wt .-%, of a gelling agent, iv) 0 to 20 wt .-% further constituents. wherein the total amount of VOC is at most 80 and preferably 55 wt .-%.

In the preparation of gels based on the polymers A, it is possible to use customary gel formers, for example in order to adjust special rheological or other performance properties of the gels. As gel formers, all gel formers customary in cosmetics can be used. These include slightly crosslinked polyacrylic acid, for example carbomer (INCI), cellulose derivatives, eg. Hydroxypropyl cellulose, hydroxyethyl cellulose, cationic modified celluloses, polysaccharides, e.g. Xanthan gum, caprylic / capric triglyceride, sodium acrylate copolymers, polyquaternium-32 (and) paraffinum liquidum (INCI), sodium acrylate copolymers (and) paraffin liquidum (and) PPG-1 trideceth-6, acrylamidopropyltrimonium chloride / Acrylamide Copolymers, Steareth-10 Allyl Ether Acrylate Copolymers, Polyquatemium-37 (and) Paraffinum Liquidum (and) PPG-1 Trideceth-6, Polyquaternium 37 (and) Propylene Glycol Dicaprate Dicaprylate (and) PPG-1 Trideceth-6, Polyquaternium 7, Polyquaternium-44. As a gelling agent suitable cross-linked homopolymers of acrylic acid are available commercially for example under the name Carbopol ^® (Noveon). Also hydrophobically modified crosslinked polyacrylate polymers, such as Carbopol ^® Ultrez 21 (Noveon) are preferred. Further examples of anionic polymers suitable as gelling agents are copolymers of acrylic acid and acrylamide and their salts; Sodium salts of polyhydroxycarboxylic acids, water-soluble or water-dispersible polyesters, polyurethanes and polyureas. Particularly suitable polymers are copolymers of (meth) acrylic acid and polyether acrylates, wherein the polyether chain is terminated with a C ₈ -C ₃₀ -alkyl radical. These include z. As acrylate / Beheneth ^ ö-methacrylate copolymers, which are commercially available as Aculyn ^® (Rohm and Haas).

In a further embodiment, the preparation according to the invention is in the form of a hair wax, ie it has a waxy consistency and contains at least one of the abovementioned waxes in an amount of preferably 0.5 to 30% by weight and optionally other water-insoluble substances. The waxy consistency is preferably characterized in that the needle penetration number (unit of measurement 0.1 mm, test weight 100 g, test duration 5 s, test temperature 25 ° C, according to DIN 51 579) is greater than or equal to 10, more preferably greater than or equal to 20 and that the solidification point of the product is preferably greater than or equal to 30 ° C and less than or equal to 70 ⁰ C, more preferably in the range of 40 to 55 ° C. Suitable waxes and water-insoluble substances are, in particular, emulsifiers with an HLB value below 7, silicone oils, silicone waxes, waxes (2.B.

Wax acids, wax esters, and in particular natural waxes such as beeswax, carnauba wax, etc.), fatty alcohols, fatty acids, fatty acid esters or hydrophilic waxes such as e.g. high molecular weight polyethylene glycols having a molecular weight of 800 to 20,000, preferably from 2,000 to 10,000 g / mol. If the cosmetic, preferably hair cosmetic preparation according to the invention is in the form of a hair lotion, it is present as a substantially non-viscous or slightly viscous, flowable solution, dispersion or emulsion containing at least 10% by weight, preferably 20 to 95% by weight. a cosmetically acceptable alcohol. As alcohols, it is possible in particular to use the lower alcohols having 1 to 4 C atoms, which are customarily used for cosmetic purposes, e.g. Ethanol and isopropanol are used.

If the hair cosmetic preparation according to the invention is in the form of a hair cream, it is preferably in the form of an emulsion and either additionally contains viscosity-imparting ingredients in an amount of from 0.1 to 10% by weight, or the required viscosity and creamy consistency are obtained by micelle formation of suitable emulsifiers, fatty acids, fatty alcohols, waxes, etc. in the usual manner.

The novel polymers A can be used as conditioning agents in cosmetic preparations. The novel polymers A can preferably be used in shampoo formulations as setting and / or conditioning agents. Preferred shampoo formulations comprise i) from 0.05 to 10% by weight of at least one polymer A, ii) from 25 to 94.95% by weight of water, iii) from 5 to 50% by weight of surfactants, iv) from 0 to 5% by weight. % of a further conditioning agent, v) 0 to 10% by weight of further cosmetic constituents.

In the shampoo formulations all anionic, neutral, amphoteric or cationic surfactants commonly used in shampoos can be used. Suitable anionic surfactants are, for example, alkyl sulfates, alkyl ether sulfates, alkyl sulfonates, alkyl aryl sulfonates, alkyl succinates, alkyl sulfosuccinates, N-alkoyl sarcosinates, acyl taurates, acyl isothionates, alkyl phosphates, alkyl ether phosphates, alkyl ether carboxylates, alpha-olefin sulfonates, in particular the alkali metal and alkaline earth metal salts, eg. As sodium, potassium, magnesium, calcium, and ammonium and Triethanolamine salts. The alkyl ether sulfates, alkyl ether phosphates and alkyl ether carboxylates can have between 1 to 10 ethylene oxide or propylene oxide units, preferably 1 to 3 ethylene oxide units in the molecule.

For example, sodium lauryl sulfate, ammonium lauryl sulfate, sodium lauryl ether sulfate, ammonium lauryl ether sulfate, sodium lauryl sarcosinate, sodium oleyl succinate, ammonium lauryl sulfosuccinate, sodium dodecylbenzenesulfonate, triethanolamine dodecylbenzenesulfonate are suitable.

Suitable amphoteric surfactants are, for example, alkylbetaines, alkylamidopropylbetaines, alkylsulfobetaines, alkylglycinates, alkylcarboxyglycinates, alkylamphoacetates or -propionates, alkylamphodiacetates or -dipropionates.

For example, cocodimethylsulfopropyl betaine, lauryl betaine, cocamidopropyl betaine or sodium cocamphopropionate can be used.

Suitable nonionic surfactants are, for example, the reaction products of aliphatic alcohols or alkylphenols having 6 to 20 C atoms in the alkyl chain, which may be linear or branched, with ethylene oxide and / or propylene oxide. The amount of alkylene oxide is about 6 to 60 moles per mole of alcohol. Also suitable are alkylamine oxides, mono- or dialkylalkanolamides, fatty acid esters of polyethylene glycols, alkylpolyglycosides or sorbitan ether esters.

In addition, the shampoo formulations may contain conventional cationic surfactants, such as. B. quaternary ammonium compounds, for example Cetyltrimethylammoni- umchlorid.

Conventional conditioning agents in combination with the polymers A can be used in the shampoo formulations to achieve certain effects. These include, for example, the abovementioned cationic polymers with the name polyquaternium according to INCI, in particular copolymers of vinylpyrrolidone /

N-vinylimidazolium salts (Luviquat ^® FC, Luviquat ^® HM, Luviquat ^® MS, Luviquat ^® Care, Luviquat ^® Ultra Care), copolymers of N-

Vinylpyrrolidone / dimethylaminoethyl methacrylate, quaternized with diethyl sulfate (Luviquat ^® PQ 11), copolymers of N-vinylcaprolactam / N-vinylpyrrolidone / N-vinylimidazolium salts (Luviquat Hold ^®); cationic cellulose derivatives (polyquaternium-4 and -10), acrylamide copolymers (polyquaternium-7). Furthermore, protein hydrolysates can be used, as well as conditioning substances based on silicone compounds, for example polyalkylsiloxanes, polyarylsiloxanes, polyarylalkylsiloxanes, polyethersiloxanes or silicone resins. Other suitable silicone compounds are dimethicone copolyols (CTFA) and amino-functional silicone compounds such as amodimethicones (CTFA). Furthermore, cationic guar derivatives such as guar hydroxypropyltrimonium chloride (INCI) can be used. measurement methods

Determination of the K value

The K values are measured according to Fikentscher, Cellulose Chemistry, Vol. 13, pages 58 to 64 (1932) at 25 ° C. in ethanol or N-methylpyrrolidone (NMP) solution and represent a measure of the molecular weight. The ethanol or NMP solutions of the polymers each contain 1 g of polymer A in 100 ml of solution.

In the case where the polymers are present in the form of aqueous dispersions, depending on the polymer content of the dispersion, appropriate amounts of the dispersion are made up to 100 ml with ethanol so that the concentration is 1 g in 100 ml.

The K value is measured in a Micro Ubbelohde capillary type M Ic from Schott.

Determine droplet size distribution (TGV) using Malvern ^® scattered light analysis

The droplet size distribution was determined using particle system for detecting liquid aerosols "Malvern ^® Master Sizer X" (Malvern Instruments Inc., Southborough MA, USA).

Measuring principle: The measuring system is based on the method of laser light diffraction on the particle, which is suitable not only for spray analysis (aerosols, pump sprays) but also for the size determination of solids, suspensions and emulsions in the size range from 0.1 μm to 2000 μm.

A particle collective (= droplet) is illuminated by a laser. At each droplet, part of the incident laser light is scattered. This light is received at a multi-element detector and the associated light energy distribution is determined. From these data, the corresponding particle distribution is calculated via the evaluation software.

Procedure: The aerosols were sprayed at a distance of 29.5 cm to the laser beam. The spray cone entered at right angles to the laser beam.

The aerosol cans were fixed to a fixed fixture before each measurement, thus ensuring that all the aerosols to be tested were measured at exactly the same distance. Before the actual particle measurement, a "background measurement" was performed, eliminating the effects of dust and other contaminants in the measurement area.

Subsequently, the aerosol was sprayed into the test room. The total particle volume was recorded and evaluated over a test period of 2 s.

Evaluation:

The evaluation contains a tabular representation over 32 class widths from 0.5μm to 2000μm and additionally a graphic representation of the particle size distribution. Since the spraying tests are approximately evenly distributed, the mean diameter is given as "Mean Diameter" D (v, 0.5), which indicates that 50% of the total measured particle volume is below this value.

In the case of sprayable aerosol systems in the cosmetic sector, this value is in the range from 30 μm to 80 μm, depending on the polymer content, valve and spray head geometry, solvent ratio and propellant gas quantities.

Determination of consolidation (flexural strength):

The consolidation of polymeric film formers was physically measured by measuring the bending stiffness of thin hair strands (each about 3 g and 24 cm in length) in addition to subjective assessment (hand test). For this purpose, the weighed, dry strands of hair were immersed in the 3.0% by weight polymer solution (solvent: ethanol / water 55:45 w / w), whereby a uniform wetting of the beads by immersing and removing three times and then pressing between filter paper Hair strand and distribution of the polymer solution was ensured. The excess film former solution was then stripped between the thumb and forefinger and the strands of hair were hand-formed into strands to give a round cross-section. At 20 ° C and 65% relative humidity was dried overnight in a climate room. The tests were carried out in a climatic chamber at 20 ° C and 65% relative humidity by means of a tensile / pressure tester. The lock of hair was placed symmetrically at the ends on two cylindrical rollers of the sample holder. Right in the middle of the strand was now bent from above with a rounded stamp about 40 mm (breaking the polymer film). The required force (Fmax) was determined with a load cell (50 N). In this case, a measured value represents the arithmetic mean of the individual measurements on 5 to 10 equally treated

Hasrstähnen dar. The values thus determined were compared to those of a commercially available comparative polymer (Amphomer ^® LV-71) and expressed in%. Determination of leachability:

An analogous to the determination of the setting polymer treated hair tress was in an approximately 37 ° C warm Texapon ^® NSO - overall solution (6ml of Texapon ^® NSO (28%) in 11 hot water) for about 15 seconds by δmaliges immersing and squeezing to wash. The hair strand was then rinsed and treated again in the same way. Thereafter, the strand of hair was well-expressed on filter paper and allowed to dry overnight. The dry strand of hair was screwed in and examined for residues.

Determination of curl retention

Basic recipe: (aerosol hairspray)

5% by weight of active substance polymer to be tested (100% neutral with AMP)

15% by weight of ethanol 40% by weight of water 40% by weight of dimethyl ether.

For the determination of curl retention hair strands of about 2 g in weight and 15.5 cm in length and from middle brown, Caucasian human hair were used.

Treatment of the hair strands: The strands of hair were washed twice with an aqueous Texapon ^® NSO solution. Subsequently, the hair strands were rinsed with warm water until no more foam was visible and rinsed with deionized water, combed and placed on filter paper to dry.

To prepare a water wave, the hair strands are placed for 15 minutes to swell in a solution of ethanol and water (1: 1).

The lock of hair was carefully combed before curling preparation. With a rubber band, the strand of hair was attached to the plexiglass rod. It was then combed and wound spirally. With a cotton cloth and rubber band, the lock was firmly fixed and dried overnight at 70 ° C. The cooled Curl Retention Strands were carefully opened and stripped off the plexiglass rod without deforming the water wave. From a distance of 15 cm was sprayed from the above-prepared aerosol hair spray 1, 8g evenly on the curl. The curl was turned evenly. In a horizontal position, the curls were dried for 1 h at room temperature. After drying, the beads were fixed in a holder. With the aid of a scale, the initial length of the curls was read at the beginning and the length extension during the wet climate storage was tracked. After 5h storage at 25 ° C and 90% RH in the climatic chamber the length of the curl was read again and the curl retention was calculated according to the following equation:

L - U curl retention in% = * 100

L - L ₀

L = length of the hair (15.5 cm) L ₀ = length of the hair curl after drying L ₁ = length of hair lock after climate treatment The mean value from the 5 individual measurements was given as curl retention.

Determination of stickiness

A clear, 20% strength by weight ethanolic or ethanolic / aqueous solution of the polymer to be characterized was first prepared. In order to obtain a clear solution, it was sometimes necessary to neutralize the polymer. From the ethanolic or ethanolic / aqueous solution, a film of the polymer was then applied to a glass plate using a doctor blade (120 μm gap width). This rectangular glass plate had a length of about 20 cm and a width of about 6.5 m. The polymer film applied thereon each had a length of about 16 to 18 cm and a width of about 5.5 cm.

The film was then dried in the air for about 10 hours and then stored in a climatic chamber at 20 ^° C. and 80% relative humidity for a further 12 hours.

Under these conditions, then in the climatic chamber on a round rubber stamp (diameter 400 mm, Shore A hardness 60 ± 5) located plastic carbon tape (eg Pelikan ^® 2060, 50 mm wide) with a force of about 250 N. pressed onto the polymer film for 10 seconds.

The amount of black pigment adhered to the polymer film after removal of the stamp corresponds to the stickiness of the film. There was a visual assessment of the black color of the film. The rating scale ranges from 0 to 5, with 0 not sticky and 5 very sticky.

Determination of the appearance of the aerosol formulation

The preparation of 5 wt .-% of the respective polymer neutralized with AMP,

40% by weight of DME, 15% by weight of ethanol and 40% by weight of water were transformed into a transesterified filled glass aerosol container. Subsequently, the clarity of the resulting liquid / gas mixture was visually evaluated.

Examples

The following examples illustrate the invention without being limited thereto. The percentages are by weight unless otherwise specified.

Used abbreviations:

MAS methacrylic acid

AS acrylic acid

MMA methyl methacrylate

Laromer® ^® BDDA butanediol

Laromer® ^® TPGDA tripropylene

Demineralized water desalinated water

Preparation of Comparative Example 1 (V1)

With stirring at 20 ^° C., the following feeds were prepared: Feed 1

111 g MMA

37.5 g of AS

100g ethanol Inlet 2

1, 5 g Wako ^® V 59 50 g of ethanol

At 20 ° C, a mixture of 150 g of ethanol, 15 wt .-% of the total amount of feed 1 and 15 wt .-% of the total amount of feed 2 were prepared. The mixture was heated to 78 ° C under normal pressure. While maintaining the polymerization temperature, feeds 1 and 2 were started after reaching 78 ° C. Feed 1 was added within 3 hours and feed 2 within 4 hours with a constant feed stream. After the end of Feed 2, the reaction mixture a further 2 h at 78 ° C was maintained and then cooled to room temperature (about 20 ⁰ C).

Preparation of Comparative Example 2 (V2)

In a 2-liter polymerization vessel with stirrer and heating and cooling devices were at a temperature of 20 to 25 ⁰ C.

400 g of deionized water

0.6 g of a 15% strength by weight aqueous solution of sodium lauryl sulfate in deionized water

Introduced 35 g of feed Il (see below) and heated to 45 ° C with stirring and nitrogen atmosphere. After reaching this temperature, feed I was added within 5 minutes. The mixture was then heated to 80 ⁰ C and added while stirring and maintaining the reaction temperature feed Il within 2.5 hours with constant feed streams. After the feeds, the reaction mixture was stirred for a further hour at 80 ⁰ C and then cooled to 60 °. While maintaining the temperature of 60 °, feed IM was added. It was then cooled to 35 ° C and while maintaining the reaction temperature feed IV was added.

Feed I:

6 g of 7% strength by weight aqueous solution of sodium persulfate in deionized water

Feed Il is an aqueous monomer emulsion prepared from:

Production Feed Il

To the initially charged deionized water was added with stirring the total amount of the 15% by weight aqueous solution of sodium lauryl sulfate. To the homogeneous solution, which was still stirred, were added in the order given the appropriate amounts of methyl methacrylate, Tween ™ 80, methacrylic acid and n-dodecylmercaptan.

Intake

Preparation of Comparative Example 3 (V3)

While stirring at 20 ^° C., the following feeds were made: Feed 1

207 g MMA

69g MAS

5.5 g Laromer® ^® BDDA

2 g of mercaptoethanol

200g ethanol Inlet 2

7 g of Wako ^® V 59

50 g of ethanol

At 20 ° C, a mixture of 300g ethanol, 15 wt .-% of the total amount of feed 1 and 15 wt .-% of the total amount of feed 2 was prepared. The mixture was heated to 78 ° C under normal pressure. While maintaining the polymerization temperature, feed 1 and feed 2 were started after reaching 78 ° C. Feed 1 was added within 3 hours and feed 2 within 4 hours with a constant feed stream. After the end of the feed 2, the reaction mixture was kept for a further 2 h at 78 ° C and then cooled to room temperature (about 20 ⁰ C).

Preparation Example 1

While stirring at 20 ° C, the following feeds were prepared

Feed 1 m g MMA

22.5 g MAS

15 g AS

100g ethanol

Inlet 2

1, 5 g Wako V 59 ^®

50 g of ethanol

At 20 ⁰ C a mixture of 150 g of ethanol, 15 wt .-% of the total amount of feed were prepared 2 the total amount of feed 1, and 15 wt .-%. The mixture was heated to 78 ° C under normal pressure. While maintaining the polymerization temperature, feed 1 and feed 2 were started after reaching the 78 ° C. Feed 1 was added within 3 hours and feed 2 within 4 hours with a constant feed stream. After the end of feed 2, the reaction mixture was kept at 78 ° C. for a further 2 h and then cooled to room temperature (about 20 ° C.).

Production Example 2

With stirring at 20 ^° C., the following feeds were prepared: Feed 1

114 g MMA 23g MAS

15.4 g of AS

1, 54 g Laromer ^{0 8} TPGDA

100g ethanol

Inlet 2

2.25 g Wako V 59 ^®

50 g of ethanol

At 20 ° C, a mixture of 150 g of ethanol, 15 wt .-% of the total amount of feed 1 and 15 wt .-% of the total amount of feed 2 was prepared. The mixture was heated to 78 ° C under normal pressure. While maintaining the polymerization temperature, feed 1 and feed 2 were started after reaching 78 ° C. Feed 1 was added within 3 hours and feed 2 within 4 hours with a constant feed stream. After the end of the feed 2, the reaction mixture was kept for a further 2 h at 78 ° C and then cooled to room temperature (about 20 ⁰ C).

Production Example 3

With stirring at 20 ° C, the following feeds were prepared:

Inlet 1

120 g MMA

15 g MAS

15 g AS

175g ethanol

Inlet 2

3 g of sodium peroxodisulfate

75 g of water

At 20 ° C, a mixture of 100 g of ethanol, 15 wt .-% of the total amount of feed 1 and 15 wt .-% of the total amount of feed 2 was prepared. The mixture was heated to 78 ° C under normal pressure. While maintaining the polymerization temperature, feed 1 and feed 2 were started after reaching 78 ° C. Feed 1 was metered in within 3 h and feed 2 within 4 h with constant feed stream. After the end of feed 2, the reaction mixture was kept at 78 ° C. for a further 2 h and then cooled to room temperature (about 20 ° C.). Production Example 4

In a 2-liter polymerization vessel with stirrer and heating and cooling devices were at a temperature of 20 to 25 ° C.

350 g of deionized water

0.8 g of a 15% by weight aqueous solution of sodium lauryl sulfate in deionized water

Introduced 35 g of feed Il (see below) and heated to 45 ° C with stirring and nitrogen atmosphere. After reaching this temperature, feed I was added within 5 minutes. The mixture was then heated to 80 ⁰ C and added while stirring and maintaining the reaction temperature feed Il within 2.5 hours with constant feed streams. After the feeds, the reaction mixture was stirred for a further hour at 80 ⁰ C and then cooled to 60 °. While maintaining the temperature of 60 °, feed IM was added. It was then cooled to 35 ° C and while maintaining the reaction temperature feed IV was added.

Feed I:

5.5 g of 7% strength by weight aqueous solution of sodium persulfate in deionized water

Feed Il is an aqueous monomer emulsion prepared from:

Production Feed Il

The total amount of the 15% strength by weight aqueous solution of sodium lauryl sulfate is added to the initially introduced deionized water with stirring. To the homogeneous solution, which was further stirred, were added in the order given the appropriate amounts of methyl methacrylate, Tween ™ 80, methacrylic acid, acrylic acid and n-dodecylmercaptan. Intake

Preparation Example 5

In a 2-liter polymerization vessel with stirrer and heating and cooling devices were at a temperature of 20 to 25 ° C.

submitted and heated to 45 ° C with stirring and nitrogen atmosphere. After reaching this temperature, feed I was added within 5 minutes. The mixture was then heated to 80 ⁰ C and added while stirring and maintaining the reaction temperature feed Il within 2.5 hours with constant feed streams. After the feeds, the reaction mixture was stirred for a further hour at 80 ⁰ C and then cooled to 60 °. While maintaining the temperature of 60 °, feed IM was added. It was then cooled to 35 ° C and while maintaining the reaction temperature feed IV was added.

Feed I:

5.5 g of 7% strength by weight aqueous solution of sodium persulfate in deionized water

Feed Il was an aqueous monomer emulsion prepared from:

Production Feed Il

To the initially charged deionized water was added with stirring the total amount of the 15% by weight aqueous solution of sodium lauryl sulfate. To the homogeneous solution, which was further stirred, the corresponding quantities of methyl acrylic acid and n-dodecyl mercaptan were in the order given methacrylate, Laromer BDDA ^®, Tween ™ 80, re methacrylic added.

Intake

Preparation Example 6

With stirring at 20 ^° C., the following feeds were prepared: Feed 1

225 g MMA

60 g MAS

15 g AS 350 g of ethanol

Inlet 2

7.5 g Wako ^® V 50 150 g deionised water

At 20 ° C., a mixture of 200 g of ethanol, 15% by weight of the total amount of feed 1 and 15% by weight of the total amount of feed 2 were prepared. The mixture was heated to 78 ° C under normal pressure. While maintaining the polymerization temperature, the feeds 1 and 2 were started after reaching 78 ° C. Feed 1 was added within 3 hours and feed 2 within 4 hours with a constant feed stream. After the end of Feed 2, the reaction mixture a further 2 h at 78 ° C was maintained and then cooled to room temperature (about 20 ⁰ C).

Production Example 7

With stirring at 20 ° C, the following feeds were prepared:

Inlet 1

240 g MMA

30 g MAS

30g AS

350 g of ethanol

Inlet 2

4.5 g Wako V 50 ^®

150 g of deionised water

At 20 ⁰ C a mixture of 200 g of ethanol, 15 wt .-% of the total amount of feed were prepared 2 the total amount of feed 1, and 15 wt .-%. The mixture was heated to 78 ° C under normal pressure. While maintaining the polymerization temperature, the feeds 1 and 2 were started after reaching 78 ° C. Feed 1 was added within 3 hours and feed 2 within 4 hours with a constant feed stream. After the end of Feed 2, the reaction mixture a further 2 h at 78 ° C was maintained and then cooled to room temperature (about 20 ⁰ C). Application properties

* Determination of the setting relative [%] to the standard Amphomer.RTM ^® LV71 ** VOC55 Aerosol:

5% of the respective polymer completely neutralized with AMP, 40% DME,

15% ethanol, 40% water; spray:

Spray head: Kosmos .020D vortex .018 "21-6443-20 (Precision Valve), valve: DPV 33876 (Precision Valve) II) Application examples

Unless stated otherwise, all the acid group-containing polymers used are 100% neutralized with AMP. "Water ad 100" means that the remaining amount of water necessary to reach a total amount of 100% by weight is added to the respective preparation The quantities% are% by weight, unless otherwise specified The abbreviation "q.s." means "quantum satis", ie adding as much of an ingredient as is necessary to achieve a desired effect The indication (solid) indicates that the amount of polymer used is calculated on the basis of the solids content, provided the polymer is in solution ,

Example 1a:

VOC 55 aerosol hair spray

[%]

Polymer from Example No. 1 (solid) 5.00

Dimethyl ether 40.00 ethanol 15.00

Water ad 100

other additives: silicone, perfume, defoamer, UV absorber

The example can be repeated in each case with the polymers 2-7 according to the invention. In each case, a VOC 55 aerosol hair spray with good properties is obtained.

Example 1 b:

VOC 55 aerosol hair spray

Polymer of Example no. 1 (solid) 3.00 Balance ^® 0/55 (Messrs. National Starch) 2.00

Dimethyl ether 40.00

Ethanol 15.00 Water ad 100

other additives: silicone, perfume, defoamer, UV absorber

The example can be repeated in each case with the polymers 2-7 according to the invention. In each case, a VOC 55 aerosol hair spray with good properties is obtained.

Example 1c:

VOC 55 aerosol hair spray

Polymer of Example no. 1 (solid) 3.00 Acudyne ^® 180 (Messrs. Rohm & Haas) 1, 00

Dimethyl ether 40.00

Ethanol 15.00

Water ad 100

other additives: silicone, perfume, defoamer, UV absorber

The example can be repeated in each case with the polymers 2-7 according to the invention. In each case, a VOC 55 aerosol hair spray with good properties is obtained.

Example 1d:

VOC 55 aerosol hair spray [%]

Polymer from Example No. 1 (solid) 3.00

Amphomer.RTM ^® LV 71 (Messrs. National Starch) 2.00

Dimethyl ether 40.00

Ethanol 15.00 water ad 100

other additives: silicone, perfume, defoamer, UV absorber The example can be repeated in each case with the polymers 2-7 according to the invention. In each case, a VOC 55 aerosol hair spray with good properties is obtained.

Example 1e:

VOC 55 aerosol hair spray

Polymer of Example no. 1 (solid) 3.00 Acudyne ^® DHR (Messrs. Rohm & Haas) 1, 00

Dimethyl ether 40.00

Ethanol 15.00

Water ad 100

other additives: silicone, perfume, defoamer, UV absorber

The example can be repeated in each case with the polymers 2-7 according to the invention. In each case, a VOC 55 aerosol hair spray with good properties is obtained.

Example 1e:

VOC 55 aerosol hair spray [%]

Polymer from Example No. 1 (solid) 3.00

^Eastman® AQ 48 (Eastman-Kodak) 2.00

Dimethyl ether 40.00

Ethanol 15.00 water ad 100

other additives: silicone, perfume, defoamer, UV absorber

The example can be repeated in each case with the polymers 2-7 according to the invention. In each case, a VOC 55 aerosol hair spray with good properties is obtained.

Example 1f: VOC 55 aerosol hair spray

Polymer from Example No. 1 (solid) 3.00

Resyn ^® 28-2930 (Messrs. National Starch) 2.00 Dimethyl ether 40.00

Ethanol 15.00

Water ad 100

other additives: silicone, perfume, defoamer, UV absorber

The example can be repeated in each case with the polymers 2-7 according to the invention. In each case, a VOC 55 aerosol hair spray with good properties is obtained.

Example 1g:

VOC 55 aerosol hair spray

[%] Polymer from Example No. 1 (solid) 3.00

^Balance® 47 (National Starch) 2.00

Dimethyl ether 40.00

Ethanol 15.00

Water ad 100

other additives: silicone, perfume, defoamer, UV absorber

The example can be repeated in each case with the polymers 2-7 according to the invention. In each case, a VOC 55 aerosol hair spray with good properties is obtained.

Example 1 h:

VOC 55 aerosol hair spray

Polymer from Example No. 1 (solid) 3.00

Aquaflex ^® SF-40 (Fa. ISP) 1, 00

Dimethyl ether 40.00 ethanol 15.00 Water ad 100

other additives: silicone, perfume, defoamer, UV absorber

The example can be repeated in each case with the polymers 2-7 according to the invention. In each case, a VOC 55 aerosol hair spray with good properties is obtained.

Example 1 i:

VOC 55 aerosol hair spray

Polymer of Example no. 1 (solid) 3.00 DynamX ^® (Fa. ISP) 1, 00

Dimethyl ether 40.00

Ethanol 15.00

Water ad 100

other additives: silicone, perfume, defoamer, UV absorber

The example can be repeated in each case with the polymers 2-7 according to the invention. In each case, a VOC 55 aerosol hair spray with good properties is obtained.

Example 2a:

VOC 55 aerosol hair spray [%]

Polymer from Example No. 1 (solid) 5.00

Dimethyl ether 35.00

Propane / butane 5.00

Ethanol 15.00 water ad 100

other additives: silicone, perfume, defoamer, UV absorber The example can be repeated in each case with the polymers 2-7 according to the invention. In each case, a VOC 55 aerosol hair spray with good properties is obtained.

Example 2b:

VOC 55 aerosol hair spray

Polymer of Example no. 1 (solid) 3.00 Balance ^® 0/55 (Messrs. National Starch) 2.00

Dimethyl ether 35.00

Propane / butane 5.00

Ethanol 15.00

Water ad 100

other additives: silicone, perfume, defoamer, UV absorber

The example can be repeated in each case with the polymers 2-7 according to the invention. In each case, a VOC 55 aerosol hair spray with good properties is obtained.

Example 2c:

VOC 55 aerosol hair spray

Polymer from Example No. 1 (solid) 3.00

Acudyne ^® 180 (Messrs. Rohm & Haas) 1, 00

Dimethyl ether 40.00 ethanol 15.00

Water ad 100

other additives: silicone, perfume, defoamer, UV absorber

The example can be repeated in each case with the polymers 2-7 according to the invention. In each case, a VOC 55 aerosol hair spray with good properties is obtained.

Example 2d: VOC 55 aerosol hair spray

[%]

Polymer of Example no. 1 (solid) 3.00 Amphomer ^® LV 71 (Messrs. National Starch) 2.00

Dimethyl ether 35.00

Propane / butane 5.00

Ethanol 15.00

Water ad 100

other additives: silicone, perfume, defoamer, UV absorber

The example can be repeated in each case with the polymers 2-7 according to the invention. In each case, a VOC 55 aerosol hair spray with good properties is obtained.

Example 2e:

VOC 55 aerosol hair spray

Polymer from Example No. 1 (solid) 3.00

Acudyne ^® DHR (Messrs. Rohm & Haas) 1, 00

Dimethyl ether 35.00 propane / butane 5.00

Ethanol 15.00

Water ad 100

other additives: silicone, perfume, defoamer, UV absorber

The example can be repeated in each case with the polymers 2-7 according to the invention. In each case, a VOC 55 aerosol hair spray with good properties is obtained.

Example 2e:

VOC 55 aerosol hair spray

[%] Polymer from Example No. 1 (solid) 3.00 ^Eastman® AQ 48 (Eastman-Kodak) 2.00

Dimethyl ether 35.00

Propane / butane 5.00

Ethanol 15.00 water ad 100

other additives: silicone, perfume, defoamer, UV absorber

The example can be repeated in each case with the polymers 2-7 according to the invention. In each case, a VOC 55 aerosol hair spray with good properties is obtained.

Example 2f:

VOC 55 aerosol hair spray

Polymer from Example No. 1 (solid) 3.00

Resyn ^® 28-2930 (Messrs. National Starch) 2.00 Dimethyl ether 35.00

Propane / butane 5.00

Ethanol 15.00

Water ad 100

other additives: silicone, perfume, defoamer, UV absorber

The example can be repeated in each case with the polymers 2-7 according to the invention. In each case, a VOC 55 aerosol hair spray with good properties is obtained.

Example 2g:

VOC 55 aerosol hair spray [%]

Polymer from Example No. 1 (solid) 3.00

^Balance® 47 (National Starch) 2.00

Dimethyl ether 35.00

Propane / butane 5.00 ethanol 15.00 Water ad 100

other additives: silicone, perfume, defoamer, UV absorber

The example can be repeated in each case with the polymers 2-7 according to the invention. In each case, a VOC 55 aerosol hair spray with good properties is obtained.

Example 2h:

VOC 55 aerosol hair spray

Polymer of Example no. 1 (solid) 3.00 Aquaflex ^® SF-40 (Fa. ISP) 1, 00

Dimethyl ether 35.00

Propane / butane 5.00

Ethanol 15.00

Water ad 100

other additives: silicone, perfume, defoamer, UV absorber

The example can be repeated in each case with the polymers 2-7 according to the invention. In each case, a VOC 55 aerosol hair spray with good properties is obtained.

Example 2i:

VOC 55 aerosol hair spray

Polymer from Example No. 1 (solid) 3.00

DynamX ^® (Fa. ISP) 1, 00

Dimethyl ether 35.00 propane / butane 5.00

Ethanol 15.00

Water ad 100

other additives: silicone, perfume, defoamer, UV absorber The example can be repeated in each case with the polymers 2-7 according to the invention. In each case, a VOC 55 aerosol hair spray with good properties is obtained.

Example 3a:

Aerosol hair spray with fluorocarbon propellants

[%] Polymer from Example No. 1 (solid) 5.00

Ethanol abs. ad 100

HFC 152A 40.00

other additives: silicone, perfume, defoamer, UV absorber

The example can be repeated in each case with the polymers 2-7 according to the invention. In each case, an aerosol hair spray with good properties is obtained.

Example 3b:

VOC 55 aerosol hair spray

Polymer of Example no. 1 (solid) 3.00 Balance ^® 0/55 (Messrs. National Starch) 2.00

Ethanol abs. ad 100

HFC 152A 40.00

other additives: silicone, perfume, defoamer, UV absorber

The example can be repeated in each case with the polymers 2-7 according to the invention. In each case, an aerosol hair spray with good properties is obtained.

Example 3c:

VOC 55 aerosol hair spray

Polymer of Example no. 1 (solid) 3.00 Acudyne ^® 180 (Messrs. Rohm & Haas) 1, 00 Ethanol abs. ad 100

HFC 152A 40.00

other additives: silicone, perfume, defoamer, UV absorber

The example can be repeated in each case with the polymers 2-7 according to the invention. In each case, an aerosol hair spray with good properties is obtained.

Example 3d:

VOC 55 aerosol hair spray

Polymer of Example no. 1 (solid) 3.00 Amphomer ^® LV 71 (Messrs. National Starch) 2.00

Ethanol abs. ad 100

HFC 152A 40.00

other additives: silicone, perfume, defoamer, UV absorber

The example can be repeated in each case with the polymers 2-7 according to the invention. In each case, an aerosol hair spray with good properties is obtained.

Example 3e:

VOC 55 aerosol hair spray

Polymer of Example no. 1 (solid) 3.00 Acudyne ^® DHR (Messrs. Rohm & Haas) 1, 00

Ethanol abs. ad 100

HFC 152A 40.00

other additives: silicone, perfume, defoamer, UV absorber

The example can be repeated in each case with the polymers 2-7 according to the invention. In each case, an aerosol hair spray with good properties is obtained.

Example 3e: VOC 55 aerosol hair spray

[%]

Polymer from Example # 1 (solid) 3.00 ^Eastman® AQ 48 (Eastman-Kodak) 2.00

Ethanol abs. ad 100

HFC 152A 40.00

other additives: silicone, perfume, defoamer, UV absorber

The example can be repeated in each case with the polymers 2-7 according to the invention. In each case, an aerosol hair spray with good properties is obtained.

Example 3f:

VOC 55 aerosol hair spray

Polymer of Example no. 1 (solid) 3.00 Resyn ^® 28-2930 (Messrs. National Starch) 2.00

Ethanol abs. ad 100

HFC 152A 40.00

other additives: silicone, perfume, defoamer, UV absorber

The example can be repeated in each case with the polymers 2-7 according to the invention. In each case, an aerosol hair spray with good properties is obtained.

Example 3g:

VOC 55 aerosol hair spray

Polymer of Example no. 1 (solid) 3.00 Balance ^® 47 (Messrs. National Starch) 2.00

Ethanol abs. ad 100

HFC 152A 40.00

other additives: silicone, perfume, defoamer, UV absorber The example can be repeated in each case with the polymers 2-7 according to the invention. In each case, an aerosol hair spray with good properties is obtained.

Example 3h:

VOC 55 aerosol hair spray

Polymer of Example no. 1 (solid) 3.00 Aquaflex ^® SF-40 (Fa. ISP) 1, 00

Ethanol abs. ad 100

HFC 152A 40.00

other additives: silicone, perfume, defoamer, UV absorber

The example can be repeated in each case with the polymers 2-7 according to the invention. In each case, an aerosol hair spray with good properties is obtained.

Example 3i:

VOC 55 aerosol hair spray

Polymer of Example no. 1 (solid) 3.00 DynamX ^® (Fa. ISP) 1, 00

Ethanol abs. ad 100

HFC 152A 40.00

other additives: silicone, perfume, defoamer, UV absorber

The example can be repeated in each case with the polymers 2-7 according to the invention. In each case, an aerosol hair spray with good properties is obtained.

Example 4:

Aerosol hair spray with fluorocarbon propellants

Polymer from Example No. 1 (solid) 5.00 Dest. Water ad 100 HFC 152A 10.00

Dimethyl ether 30.00

Ethanol abs. 30.00

other additives: silicone, perfume, defoamer, UV absorber

The example can be repeated in each case with the polymers 1-11 and 13-15. In each case, an aerosol hair spray with good properties is obtained.

Example 5:

VOC 55 aerosol hair spray

Polymer of Example no. 1 (solid) 3.00 Ultrahold ^® strand (solid, Fa. BASF) 1, 00

Dimethyl ether 40.00

Ethanol 15.00

+ AMP to pH 8.3

Water ad 100

further addition: silicone, perfume, defoamer

The example can be repeated in each case with the polymers 2-7 according to the invention. In each case, a VOC 55 aerosol hair spray with good properties is obtained.

Example 6:

VOC 55 aerosol hair spray [%]

Polymer from Example No. 1 (solid) 3.00

Luvimer ^® Pro55 (solid, Fa. BASF) 1, 00

Dimethyl ether 40.00

Ethanol 15.00 water ad 100

further addition: silicone, perfume, defoamer The example can be repeated in each case with the polymers 2-7 according to the invention. In each case, a VOC 55 aerosol hair spray with good properties is obtained.

Example 7:

VOC 55 aerosol hair spray

Polymer of Example no. 1 (solid) 3.00 Luvimer ^® polyurethane (solid, Fa. BASF) 1, 00

Dimethyl ether 40.00

Ethanol 15.00

Water ad 100

further addition: silicone, perfume, defoamer

The example can be repeated in each case with the polymers 2-7 according to the invention. In each case, a VOC 55 aerosol hair spray with good properties is obtained.

Example 8:

VOC 55 aerosol hair spray

[%] Polymer from Example No. 1 (solid) 3.00

Resyn ^® 28-2930 (solid, Messrs. National Starch) 1, 00

Dimethyl ether 40.00

Ethanol 15.00

Water ad 100

further addition: silicone, perfume, defoamer

The example can be repeated in each case with the polymers 2-7 according to the invention. A VOC 55 aerosol hairspray with good properties is also obtained.

Example 9:

VOC 55 aerosol hair spray [%] Polymer from Example No. 1 (solid) 2.00

Stepanhold ^{® R-1} *} (Fa. Stepan Chemical Co.) 1 00

Dimethyl ether 40.00

Ethanol 15.00

+ AMP to pH 8.3

Water ad 100

further addition: silicone, perfume, defoamer

^*} Stepanhold ^® R-1 = poly (vinylpyrrolidone / ethyl methacrylate / methacrylic acid)

The example can be repeated in each case with the polymers 2-7 according to the invention. In each case, a VOC 55 aerosol hair spray with good properties is obtained.

Example 10:

VOC 55 hand pump spray

[%] Polymer from Example No. 1 (solid) 7.00

Ethanol 55.00

Water ad 100

further addition: silicone, perfume, defoamer

The example can be repeated in each case with the polymers 2-7 according to the invention. In each case a VOC 55 hand pump spray with good properties is obtained.

Example 11:

VOC 80 aerosol hair spray

[%]

Polymer from Example No. 1 (solid) 12.00

Dimethyl ether 40.00

Ethanol 40.00

Water ad 100

further addition: silicone, perfume, defoamer The example can be repeated in each case with the polymers 2-7 according to the invention. In each case, a VOC 80 aerosol hairspray with good properties is obtained.

Example 11:

Aqueous hand pump spray [%]

Polymer from Example No. 1 (solid) 4.00

Luviset ^® Clear ^*) (solid) 1, 00 water ad 100

further addition: water-soluble silicone, perfume, defoamer. ^η Luviset ^® Clear: poly (vinylpyrrolidone / methacrylamide / vinylimidazole), BASF Fa.

The example can be repeated in each case with the polymers 2-7 according to the invention. In each case, an aqueous hand pump spray with good properties is obtained.

Example 12:

Aqueous / ethanolic solid solution [%]

Polymer from Example No. 1 (solid) 7.00 dist. Water ad 100

Ethanol 52.00

further addition: silicone, perfume, defoamer

The example can be repeated in each case with the polymers 2-7 according to the invention. In each case a Festiger solution with good properties is obtained.

Example 13:

Ethanolic solid solution [%]

Polymer from Example No. 1 (solid) 7.0 ethanol ad 100

further addition: silicone, perfume, defoamer ...

The example can be repeated in each case with the polymers 2-7 according to the invention. In each case a Festiger solution with good properties is obtained. Example 14:

Hair gel with Aculyn 28: [%] Phase 1:

Polymer from Example No. 1 (solid) 6.00

Aminomethylpropanol (38% solution) 1, 0

Water, dist. ad 50

further additive: preservative, soluble ethoxylated silicone, perfume ...

Phase 2:

Aculyn 28 (1% aqueous suspension) 50.00

production:

Phases 1 and 2 are weighed and homogenized separately. Then phase 2 is slowly stirred into phase 1. It forms a substantially clear, stable gel.

The example can be repeated in each case with the polymers 2-7 according to the invention. Each hair gel is obtained with Aculyn 28 with good properties.

Example 15:

Hair Gel with Hydroxyethylcellulose: [%] Phase 1:

Polymer from Example No. 1 (solid) 6.00 water, dist. ad 50

further addition: preservative, soluble ethoxylated silicone, perfume

Phase 2: Natrosol HR 250 (5% solution) 50.00

Hydroxyethylcellulose (Hercules)

production: Phases 1 and 2 are weighed and homogenized separately. Then phase 2 is slowly stirred into phase 1. It forms a substantially clear, stable gel.

The example can be repeated in each case with the polymers 2-7 according to the invention. In each case, a hair gel with hydroxyethyl cellulose having good properties is obtained.

Example 16:

Foam conditioner [%]

Polymer from Example No. 1 (solid) 0.50

Cremophor ^® A 25 (Ceteareth 25 / BASF Fa.) 0.20

Comperlan® ^® KD (Coamide DEA / Fa. Henkel) 0.10 propane / butane 10.00

further addition: perfume, preservative

Water ad 100

Preparation: Weigh out and dissolve with stirring. Fill up and add propellant gas.

The example can be repeated in each case with the polymers 2-7 according to the invention. In each case, a foam conditioner with good properties is obtained.

Example 17:

Conditioner shampoo: [%]

A) Texapon ^® NSO 28 Henkel)% ig (sodium laureth sulfate / Fa. 50.00 Comperlan ^® KS (Coamid DEA / Fa. Henkel) 1, 00

Polymer from Example No. 1 (solid) 3.00 q. s. perfume oil

B) water 44.5 sodium chloride 1, 5 q. s. preservative

production: Phases 1 and 2 are weighed and homogenized separately. Then phase 2 is slowly stirred into phase 1. It forms a substantially clear, stable gel.

The example can be repeated in each case with the polymers 2-7 according to the invention. It will receive a conditioner shampoo with good properties.

Example 18:

Standard O / W cream:

oil phase: [%] CTFA name

Cremophor ^® A6 3.5 Ceteareth-6 (and) Stearyl Alcohol

Cremophor ^® A25 3.5 Ceteareth-25

Glycerol monostearate s.e. 2.5 glyceryl stearate

Paraffin oil 7.5 Paraffin OiI

Cetyl Alcohol 2.5 Cetyl Alcohol

Luvitol ^® EHO 3.2 Cetearyl octanoate

Vitamin E acetate 1, 0 tocopheryl acetate

Nip-Nip 0.1 methyl and propyl 4-hydroxybenzoates

(7: 3)

Water phase:

Polymer from Example No. 1 (solid) 0.6 water 77.0

1, 2-Propylene glycol 1, 5 Propylene glycol Germall II 0.1 imidazolidinyl urea

production:

The oil and water phases are weighed separately and homogenized at a temperature of about 80 ⁰ C. Then, the water phase is slowly stirred into the oil phase and slowly cooled to room temperature while stirring.

The example can be repeated in each case with the polymers 2-7 according to the invention. In each case a standard O / W cream with good properties is obtained. Example 19: Liquid Makeup

A

1, 70 glyceryl stearate

1, 70 cetyl alcohol

1, 70 Ceteareth-6

1, 70 Ceteareth-25

5.20 caprylic / capric triglyceride

5.20 mineral oil

B q.s. preservative

4.30 g propylene glycol

2.50 polymer from Example 1 (solid) ad 100 dist. water

C q.s. perfume oil

D

2.00 iron oxide

12.00 titanium dioxide

production:

Heat Phase A and Phase B separately to 80 ° C. Then mix phase B in phase A with a stirrer. Allow to cool to 40 ° C and add Phase C and Phase D. Homogenize repeatedly.

The example can be repeated in each case with the polymers 2-7 according to the invention. There will be a liquid makeup with good properties.

Example 20: oil-free makeup

A

0.35 Veegum

5.00 butylene glycol

0.15 xanthan gum B

34.0 dist. Water q.s. preservative

0.2 polysorbate-20

1, 6 Tetrahydroxypropylethylenediamin

C

1, 0 silica

2.0 nylon 12th

4.15 mica

6.0 Titanium Dioxide

1, 85 iron oxide

D

4.0 stearic acid

1, 5 glyceryl stearate

7.0 Benzyl laurate

5.0 Isoeicosan q.s. preservative

e

0.5 panthenol

0.1 imidazolidinyl urea

5.0 Polymer from Example 1 (solid)

production:

Coat phase A with butylene glycol, add to phase B and mix well. Heat phase AB to 75 ° C. Pulverize phase C feedstocks, add to phase AB and homogenize well. Mix the starting materials of phase D, heat to 80 ° C and add to phase ABC. Mix for a while until everything is homogenous. Transfer everything to a vessel with a propeller mixer. Mix phase E starting materials, add to phase ABCD and mix well.

The example can be repeated in each case with the polymers 2-7 according to the invention. There will be an oil-free makeup with good properties.

Example 21: Shimmering gel

A 32.6 dist. water

0.1 disodium EDTA

25.0 Natrosol (4% aqueous solution)

0.3 preservative

B

0.5 dist. water

0.5 triethanolamine

C

2.0 polymer from Example 1 (solid) ad 100 dist. water

1, 0 Polyquaternium-46 (20% aqueous solution)

5.0 iron oxide

D

15.0 dist. water

1, 0 D-panthenol 50 P (panthenol and propylene glycol)

production:

Using a propeller mixer, mix the starting materials of phase A well in the order listed. Then add phase B to phase A. Stir slowly until everything is homogeneous. Homogenise Phase C well until the pigments are well dispersed. Add phase C and phase D to phase AB and mix well.

The example can be repeated in each case with the polymers 2-7 according to the invention. In each case, a shimmering gel with good properties is obtained.

Example 22: Sunscreen Gel

Phase A

1, 00 hydrogenated castor oil-PEG-40

8.00 Octyl Methoxycinnamate (Uvinul ^® MC 80)

5.00 Octocrylene (Uvinul ^® N 539)

0.80 Octyl Triazone (Uvinul ^® T 150)

2.00 Butyl Methoxydibenzoylmethane (BMBM Uvinul ^®)

2.00 tocopheryl acetate qs perfume oil Phase B

2.50 polymer from Example 1 (solid) ad 100 dist. water

0.30 acrylate / Cio ₃ oAlkylacrylat copolymer

0.20 carbomer

5.00 glycerol

0.20 disodium EDTA q.s. preservative

62.80 dist. water

Phase C

0.20 sodium hydroxide

Preparation: Mix the components of phase A. Swell phase B and stir in phase A with homogenization. Neutralize with Phase C and homogenize again.

The example can be repeated in each case with the polymers 2-7 according to the invention. In each case a sunscreen gel with good properties is obtained.

Example 23: Sunscreen emulsion with TiO ₂ and ZnO ₂

Phase A

6.00 hydrogenated castor oil PEG-7

2.00 PEG-45 / dodecyl glycol copolymer

3.00 isopropyl myristate

8.00 jojoba oil (Buxus chinensis)

4.00 Octyl Methoxycinnamate (Uvinul ^® MC 80)

2.00 4-Methylbenzylidene Camphor (Uvinul ^® MBC 95)

3.00 titanium dioxide, dimethicone

1, 00 Dimethicone

5.00 zinc oxide, dimethicone

Phase B

2.0 polymer from Example 1 (solid) ad 100 dist. water

0.20 disodium EDTA

5.00 glycerin qs preservative 50.80 dist. water

Phase C q.s. perfume oil

production:

Heat phases A and B separately to approx. 85 ° C. Stir phase B into phase A and homogenize. Cool to about 40 ° C, add phase C and briefly homogenize again.

The example can be repeated in each case with the polymers 2-7 according to the invention. In each case, a sunscreen emulsion with TiO ₂ and ZnO ₂ with good properties is obtained.

Example 24: Sunscreen Lotion

Phase A

6.00 Octyl Methoxycinnamate (Uvinul ^® MC 80) 2.50 4-Methylbenzylidene Camphor (Uvinul ^® MBC 95)

1, 00 Octyl Triazone (Uvinul ^® T 150)

2.00 Butyl Methoxydibenzoylmethane (BMBM Uvinul ^®)

2.00 PVP / hexadecene copolymer

5.00 PPG-3 myristyl ether 0.50 dimethicone

0.10 BHT, ascorbyl palmitate, citric acid, glyceryl stearate, propylene glycol

2.00 cetyl alcohol

2.00 potassium cetyl phosphate

Phase B

0.50 polymer of Example 1 (solid) ad 100 dist. water

5.00 propylene glycol 0.20 disodium EDTA q.s. preservative

63.92 dist. water

Phase C 5.00 mineral oil 0.20 carbomer

Phase D

0.08 sodium hydroxide

Phase E q.s. perfume oil

production:

Heat phases A and B separately to approx. 80 ° C. Stir phase B into phase A while homogenizing, after-homogenize shortly. Stir phase C, stir in phase AB, neutralize with phase D and posthumogenize. Cool to about 40 ° C, add phase E, homogenize again.

The example can be repeated in each case with the polymers 2-7 according to the invention. In each case, a sunscreen lotion with good properties is obtained.

Example 25: Peelable Face Mask

Phase A

57.10 dist. water

6.00 polyvinyl alcohol 5.00 propylene glycol

Phase B

20.00 alcohol

4.00 PEG-32 q.s perfume oil

Phase C

5.00 Polyquaternium-44

0.50 polymer of Example 1 (solid) ad 100 dist. water

0.20 allantoin

production: Heat phase A to at least 90 ° C and stir until dissolved. Dissolve phase B at 50 ° C and stir into phase A. At approx. 35 ° C, compensate for the loss of ethanol. Add phase C and stir.

The example can be repeated in each case with the polymers 2-7 according to the invention. In each case, a peelable face mask with good properties is obtained.

Example 26: Face Mask

Phase A

3.00 Ceteareth-6

1, 50 Ceteareth-25

5.00 Cetearyl alcohol

6.00 Cetearyl octanoate

6.00 mineral oil

0.20 bisabolol

3.00 glyceryl stearate

Phase B

2,00 propylene glycol

5,00 Panthenol

2.50 polymer from Example 1 (solid) ad 100 dist. Water q.s. preservative

53.80 dist. water

Phase C q.s. perfume oil

0.50 tocopheryl acetate

production:

Heat phase A and B separately to approx. 80 ° C. Stir phase B into phase A while homogenizing, shortly after homogenizing. Cool to about 40 ° C, add phase C, homogenize again.

The example can be repeated in each case with the polymers 2-7 according to the invention. In each case a face mask with good properties is obtained. Example 27: Body Lotion Foam

Phase A

1, 50 Ceteareth-25

1, 50 Ceteareth-6

4.00 Cetearyl alcohol

10.00 Cetearyl octanoate

1, 00 Dimethicone

Phase B

0.50 polymer of Example 1 (solid) ad 100 dist. water

2,00 Panthenol

2.50 g propylene glycol q.s. preservative

74.50 dist. water

Phase C q.s. perfume oil

production:

Heat phases A and B separately to approx. 80 ° C. Stir phase B into phase A and homogenize. Cool to about 40 ° C, add phase C and briefly homogenize again. Bottling: 90% active ingredient and 10% propane / butane at 3.5 bar (20 ⁰ C).

The example can be repeated in each case with the polymers 2-7 according to the invention. In each case, a body lotion foam having good properties is obtained.

Example 28: Toner for dry and sensitive skin

Phase A

2.50 hydrogenated castor oil PEG-40 q.s. perfume oil

0.40 bisabolol

Phase B

3.00 glycerol 1, 00 hydroxyethyl cetyldimonium phosphate

5.00 Witch hazel (Hamamelis Virginiana) distillate

0.50 panthenol

0.1 polymer of Example 1 (solid) ad 100 dist. Water q.s. preservative

87.60 dist. water

production:

Clear phase A clearly. Stir phase B into phase A.

The example can be repeated in each case with the polymers 2-7 according to the invention. In each case, a toner for dry and sensitive skin with good properties is obtained.

Example 29: Face wash paste with peeling effect

Phase A

58.00 dist. water

2.50 polymer from Example 1 (solid) ad 100 dist. water

1.50 carbomer q.s. preservative

Phase B q.s. perfume oil

7.00 Potassium Cocoyl Hydrolyzed Protein

4.00 Cocamidopropyl betaine

Phase C

1, 50 triethanolamine

Phase D

13.00 polyethylene (Luwax ^® A)

production:

Let phase A swell. Clear phase B clearly. Stir phase B into phase A. Neutralize with Phase C. Then stir in phase D. The example can be repeated in each case with the polymers 2-7 according to the invention. In each case, a facial scrubbing paste with peeling effect with good properties is obtained.

Example 30: Facial soap

Phase A

25.0 potassium cocoate

20.0 Disodium Cocoamphodiacetate

2.0 Lauramide DEA

1, 0 glycol stearate

0.50 polymer of Example 1 (solid) ad 100 dist. water

50.0 dist. Water q.s. citric acid

Phase B q.s. Preservatives q.s. perfume oil

production:

Heat phase A to 70 ^° C. while stirring until everything is homogeneous, adjust the pH to 7.0 7.5 with citric acid, allow to cool to 50 ^° C. and add phase B.

The example can be repeated in each case with the polymers 2-7 according to the invention. It will receive a facial soap with good properties.

Example 31: Facial cleansing milk, type O / W

Phase A

1, 50 Ceteareth-6

1, 50 Ceteareth-25

2.00 glyceryl stearate

2.00 cetyl alcohol

10.00 mineral oil

Phase B S

5.00 g propylene glycol q.s. preservative

1, 0 polymer of Example 1 (solid) ad 100 dist. Water 62.30 dist. water

Phase C

0.20 carbomer

10.00 Cetearyl octanoate

Phase D

0.40 tetrahydroxypropylethylenedi

Phase E q.s. perfume oil

0.10 bisabolol

production:

Heat phases A and B separately to approx. 80 ° C. Stir phase B into phase A while homogenizing, after-homogenize shortly. Stir phase C, stir in phase AB, neutralize with phase D and posthumogenize. Cool to about 40 ° C, add phase E, homogenize again.

The example can be repeated in each case with the polymers 2-7 according to the invention. In each case, a facial cleansing milk type O / W with good properties is obtained.

Example 32: Peeling cream, type O / W

Phase A

3.00 Ceteareth-6

1, 50 Ceteareth-25

3.00 glyceryl stearate 5.00 cetearyl alcohol, sodium cetearyl sulphate

6.00 Cetearyl octanoate

6.00 mineral oil

0.20 bisabolol

Phase B 2,00 propylene glycol

0.10 disodium EDTA

0.50 polymer of Example 1 (solid) ad 100 dist. Water q.s. preservative

59.70 dist. water

Phase C

0.50 tocopheryl acetate q.s. perfume oil

Phase D

10.00 polyethylene

production:

Heat phases A and B separately to approx. 80 ° C. Stir phase B into phase A and homogenize. Cool to about 40 ° C, add phase C and briefly homogenize again. Then stir in phase D.

The example can be repeated in each case with the polymers 2-7 according to the invention. In each case a scrub cream type O / W with good properties is obtained.

Example 33: Shaving cream

6.00 Ceteareth-25

5.00 Poloxamer 407

52.00 dist. water

1, 00 triethanolamine

5.00 propylene glycol

1.00 lanolin-PEG-75

1, 0 polymer of Example 1 (solid) ad 100 dist. Water q.s. Preservatives q.s. perfume oil

25.00 Sodium Laureth Sulfate

production: Weigh everything together, then stir until dissolved. Filling: 90 parts of active substance and 10 parts of propane / butane mixture 25:75.

The example can be repeated in each case with the polymers 2-7 according to the invention. In each case, a shaving foam with good properties is obtained.

Example 34: After Shave Balm

Phase A

0.25 acrylate / Cio-3o alkyl acrylate copolymer

1, 50 tocopheryl acetate

0.20 bisabolol

10.00 caprylic / capric triglyceride q.s. perfume oil

1, 00 hydrogenated castor oil-PEG-40

Phase B

1, 00 panthenol

15.00 alcohol

5.00 glycerol

0.05 hydroxyethylcellulose

0.50 polymer of Example 1 (solid) ad 100 dist. water

64.00 dist. water

Phase C

0.08 sodium hydroxide

production:

Mix the components of phase A. Stir phase B into phase A while homogenizing, after-homogenize shortly. Neutralize with Phase C and homogenize again.

The example can be repeated in each case with the polymers 2-7 according to the invention. In each case an aftershave balm with good properties is obtained.

Example 35: Body Care Cream Phase A

2.00 ceteareth-6

2.00 Ceteareth-25

2.00 Cetearyl alcohol

3.00 glyceryl stearate SE

5.00 mineral oil

4.00 jojoba oil (Buxus chinensis)

3.00 Cetearyl octanoate

1, 00 Dimethicone

3.00 mineral oil, lanolin alcohol

Phase B

5.00 propylene glycol

0,50 Veegum

1, 00 panthenol

1, 70 polymer from Example 1 (solid) ad 100 dist. water

6.00 Polyquaternium-44 (10% aqueous solution) q.s. preservative

54.00 dist. water

Phase C q.s. perfume oil

production:

Heat phases A and B separately to approx. 80 ° C. Homogenize phase B. Stir phase B into phase A while homogenizing, after-homogenize shortly. Cool to about 40 ° C, add phase C and briefly homogenize again.

The example can be repeated in each case with the polymers 2-7 according to the invention. It will receive a personal care cream with good properties.

Example 36: Toothpaste

Phase A 34.79 dist. Water 0.50 Polymer from Example 1 (solid) ad 100 dist. Water 0.30 preservative 20.00 glycerol

0.76 sodium monofluorophosphate

Phase B

1, 20 Sodium carboxymethylcellulose €

Phase C

0.80 aromatic oil

0.06 saccharin

0.10 preservative

0.05 bisabolol

1, 00 panthenol

0.50 tocopheryl acetate

2.80 silica

1, 00 sodium lauryl sulfate

7,90 Dicalcium phosphate, anhydrous

25.29 dicalcium phosphate dihydrate

0.45 titanium dioxide

production:

Solve phase A. Place phase B in phase A and dissolve. Add phase C and allow to stir under vacuum at RT for approx. 45 min.

The example can be repeated in each case with the polymers 2-7 according to the invention. In each case a toothpaste with good properties is obtained.

Example 37: Mouthwash

Phase A

2.00 aromatic oil

4.00 hydrogenated castor oil PEG-40

1, 00 Bisabolol

30.00 alcohol

Phase B

0.20 saccharin

5.00 Glycerin qs Preservative 5.00 Poloxamer 407 0.50 polymer of Example 1 (solid) ad 100 dist. water

production:

Separate phase A and phase B separately. Stir phase B into phase A.

The example can be repeated in each case with the polymers 2-7 according to the invention. In each case, a mouthwash with good properties is obtained.

Example 38: Denture adhesive

Phase A 0.20 bisabolol

1, 00 beta carotene q.s. aromatic oil

20.00 Cetearyl octanoate

5.00 silica 33.80 mineral oil

Phase B

1, 0 polymer of Example 1 (solid) ad 100 dist. Water 35.00 PVP (20% solution in water)

production:

Mix phase A well. Stir phase B into phase A.

The example can be repeated in each case with the polymers 2-7 according to the invention. In each case, a denture adhesive with good properties is obtained.

Example 39: Skin Care Cream, Type O / W

Phase A

8.00 Cetearyl alcohol

2.00 Ceteareth-6 2.00 Ceteareth-25 1ι

10.00 mineral oil

5.00 Cetearyl octanoate

5.00 Dimethicon

Phase B

0.50 polymer of Example 1 (solid) ad 100 dist. water

2,00 panthenol, propylene glycol q.s. preservative

Phase C q.s. perfume oil

production:

Heat phase A and B separately to approx. 80 ° C. Stir phase B into phase A while homogenizing, shortly after homogenizing. Cool to about 40 ° C, add phase C, homogenize again.

The example can be repeated in each case with the polymers 2-7 according to the invention. In each case a skin care cream, type O / W with good properties is obtained.

Example 40: Skin Care Cream, Type W / O

Phase A

6.00 hydrogenated castor oil PEG-7

8.00 Cetearyl octanoate

5.00 isopropyl myristate

15.00 mineral oil

2.00 PEG-45 / dodecyl glycol copolymer

0.50 magnesium stearate

0.50 aluminum stearate

Phase B

3.00 glycerol

0.60 polymer from Example 1 (solid) ad 100 dist. water

0.70 magnesium sulfate

2,00 Panthenol qs preservative

Phase C

1, 00 tocopherol 5.00 tocopheryl acetate q.s. perfume oil

production:

Heat phases A and B separately to approx. 80 ° C. Stir phase B into phase A and homogenize. Cool to about 40 ° C, add phase C and briefly homogenize again.

The example can be repeated in each case with the polymers 2-7 according to the invention. In each case a skin care cream, type W / O with good properties is obtained.

Example 41: Lip care cream

Phase A

10.00 Cetearyl octanoate

5.00 polybutene

Phase B

0.10 carbomer

Phase C

2.00 ceteareth-6

2.00 Ceteareth-25

2.00 glyceryl stearate

2.00 cetyl alcohol

1, 00 Dimethicone

1, 00 Benzophenone-3

0.20 bisabolol

6.00 mineral oil

Phase D

1, 50 polymer from Example 1 (solid) ad 100 dist. water

3,00 Panthenol 3,00 propylene glycol qs preservative

Phase E 0.10 triethanolamine

Phase F

0.50 tocopheryl acetate

0.10 tocopherol q.s. perfume oil

production:

Clear phase A clearly. Add phase B and homogenize. Add phase C and melt at 80 ° C. Heat phase D to 80 ° C. Add phase D to phase ABC and homogenize. Cool to about 40 ° C, add phase E and phase F, homogenize again.

The example can be repeated in each case with the polymers 2-7 according to the invention. It will each receive a lip balm with good properties.

Example 42: shower gel

50.00 Sodium Laureth Sulfate, Magnesium Laureth Sulfate, Sodium Laureth-δ Sulfate, Magnesium Laureth-δ

1, 00 Cocoamide DEA

0.8 polymer from Example 1 (solid) ad 100 dist. water

2.00 Sodium Laureth Sulfate, Glycol Distearate, Cocamide MEA, Laureth-10 q.s. Preservatives q.s. perfume oil

2.00 sodium chloride

Preparation: Weigh all components together and stir until dissolved.

The example can be repeated in each case with the polymers 2-7 according to the invention. It will receive a shower gel with good properties.

Example 43: shower gel 30.00 Sodium Laureth Sulfate

6.00 Sodium Cocoamphodiacetate

6.00 Cocamidopropyl betaine 3.00 Sodium Laureth Sulfate, Glycol Distearate, Cocamide MEA, Laureth-10

7.70 Polyquaternium-44

0.2 polymer from Example 1 (solid) ad 100 dist. water

1, 00 Panthenol q.s. Preservatives q.s. Perfume oil q.s. citric acid

0.50 sodium chloride

production:

Weigh and solve the components of phase A. Adjust the pH to 6 to 7.

The example can be repeated in each case with the polymers 2-7 according to the invention. It will receive a shower gel with good properties.

Example 44: Clear shower gel

40.00 Sodium Laureth Sulfate

5.00 decylglucoside

5.00 cocamidopropyl betaine

0.50 polyquaternium-10

2.00 polymer from Example 1 (solid) ad 100 dist. water

1, 00 Panthenol q.s. Perfume oil q.s. Preservatives q.s. citric acid

2.00 sodium chloride

production:

Weigh in the components of phase A and dissolve clearly. The example can be repeated in each case with the polymers 2-7 according to the invention. It will receive a clear shower gel with good properties.

Example 45: shower bath

A

40.00 Sodium Laureth Sulfate

5.00 Sodium Ci ₂ -i ₅ Pareth-15 Sulfonates

5.00 decylglucoside q.s. perfume oil

0.10 phytantriol

B

0.1 guar hydroxypropyltrimonium chloride

2.00 polymer from Example 1 (solid) ad 100 dist. water

1, 00 Panthenol q.s. preservative

1, 00 Laureth-3 q.s. citric acid

2.00 sodium chloride

production:

Mix the components of phase A. Add the components of phase B one after the other and mix. Adjust the pH to 6 to 7.

The example can be repeated in each case with the polymers 2-7 according to the invention. There will be a shower room with good features.

Example 46: Liquid Soap

A

43,26 dist. Water 0.34 aminomethylpropanol

3.40 Poly (ethyl acrylate / methacrylic acid) (Luviflex Soft ^®, Fa. BASF)

B

40,00 Sodium Laureth Sulfate 10,00 Cocamidopropylbetaine 0.2 polymer from Example 1 (solid) ad 100 dist. Water qs perfume oil qs preservative

2.00 sodium chloride

production:

Weigh in the components of phase A and dissolve clearly. Add the components of phase B one after the other and mix.

The example can be repeated in each case with the polymers 2-7 according to the invention. In each case, a liquid soap with good properties is obtained.

Example 47: Liquid Footbath

A

1, 00 nonoxynol-14

0.10 bisabolol

1, 00 pine oil (Pinus Sylvestris)

B

5.00 PEG-8

1, 50 polymer from Example 1 (solid) ad 100 dist. water

0.50 triclosan

30.00 Sodium Laureth Sulfate

3.00 Polyquaternium-16 q.s. C l. 19 140 + C. 1. 42 051

production:

Solubilize phase A. Mix phase B.

The example can be repeated in each case with the polymers 2-7 according to the invention. In each case, a liquid foot bath with good properties is obtained.

Example 48: Refreshing gel

A 0.60 carbomer 45.40 dist. water

B

0.50 bisabolol 0.50 farnesol q.s. perfume oil

5.00 PEG-40 Hydrogenated Castor OiI

0.50 polymer of Example 1 (solid) ad 100 dist. Water 1, 00 Tetrahydroxypropylethylendiamin

1, 50 menthol

43.00 Alcohol q.s. C.I. 74 180, Direct Blue 86

production:

Let phase A swell. Solve phase B. Stir phase B into phase A.

The example can be repeated in each case with the polymers 2-7 according to the invention. It will receive a refreshing gel with good properties.

Example 49: Roll-on antiperspirant

A

0.40 hydroxyethylcellulose

50.00 dist. water

B

25.00 alcohol

0.10 bisabolol

0.30 farnesol

2.00 PEG-40 Hydrogenated Castor OiI q.s. perfume oil

C

5.00 aluminum chlorohydrate

3.00 propylene glycol

3.00 Dimethicone copolyol

3.00 Polyquaternium-16

1, 50 polymer from Example 1 (solid) ad 100 dist. water

production:

Let phase A swell. Solve phase B and C separately. Stir phase A and B into phase C.

The example can be repeated in each case with the polymers 2-7 according to the invention. In each case a roll-on antiperspirant with good properties is obtained.

Example 50: Transparent Deodorant Stick

5.00 sodium stearate

0.50 triclosan

3.00 Ceteareth-25

20.00 glycerol

0.50 polymer of Example 1 (solid) ad 100 dist. Water q.s. perfume oil

60.00 propylene glycol

0.20 bisabolol

production:

Weigh phase A, melt and homogenize. Then pour into the mold.

The example can be repeated in each case with the polymers 2-7 according to the invention. In each case, a transparent deodorant stick with good properties is obtained.

Example 51: Water-soluble bath oil

15.00 Cetearyl octanoate

15.00 caprylic / capric triglyceride

1, 00 panthenol, propylene glycol

0.10 bisabolol

2.00 tocopheryl acetate

2.00 Retinyl palmitate 0.10 tocopherol

37.00 PEG-7-glyceryl-cocoate

0.4 polymer from Example 1 (solid) ad 100 dist. Water q.s. perfume oil

23.60 PEG-40 Hydrogenated Castor OiI

production:

Mix and stir until everything is clear.

The example can be repeated in each case with the polymers 2-7 according to the invention. In each case, a water-soluble bath oil with good properties is obtained.

Example 52: Day Care Aerosol

A

4.00 ethylhexyl methoxycinnamate

1, 50 octocrylene

9.00 caprylic / capric triglyceride

5.00 Simmondsia Chinensis (Jojoba) Seed OiI

1, 50 cyclomethicone

3.00 Hydrogenated Coco-Glycerides

1, 00 PVP / hexadecene copolymer

1, 00 Ceteareth-6, stearyl alcohol

B

5.00 zinc oxide

C

2.00 Ceteareth-25

1, 20 panthenol

0.20 Sodium Ascorbyl Phosphate

0.30 imidazolidinyl urea

0.10 Disodium EDTA

1, 50 polymer from Example 1 (solid) ad 100 dist. water

D 0.50 tocopheryl acetate

0.20 bisabolol

0.33 caprylic / capric triglyceride, retinol q.s. perfume oil

production:

Heat phase A to 80 ° C. Clear phase A clearly. Incorporate phase B and homogenize. Add phase C, heat to 80 ° C., melt and homogenize. Cool with stirring to about 40 ° C, add phase D and briefly homogenize. 90% of active ingredient solution: fill 10% propane / butane with 3,5 bar (20 ⁰ C).

The example can be repeated in each case with the polymers 2-7 according to the invention. In each case, a day care aerosol with good properties is obtained.

Example 53: Moisturizer

A

3.001 Vitis Vinifera (Grape) Seed OiI

1, 00 cyclopentasiloxane, cyclohexasiloxane

1, 50 cyclomethicone

2.00 Soybean (Glycine Soy) OiI 2.00 Ethylhexyl Methoxycinnamate

1, 00 Uvinul ^® A Pius

1, 00 Hydrogenated lecithin

1, 00 cholesterol

2.00 PEG-40 Hydrogenated Castor OiI 5.00 Cetearyl octanoate

5.00 caprylic / capric triglyceride

B

3.00 Caprylic / capric triglyceride, acrylate copolymer

C

2.50 polymer from Example 1 (solid) ad 100 dist. water

0.50 cocotrimonium methsulfate 2.00 panthenol, propylene glycol 3.00 glycerol

0.10 disodium EDTA

D 0.30 perfume oil

0.30 DMDM Hydantoin

1, 00 tocopheryl acetate

2.00 tocopherol

production:

Heat phase A to 80 ° C. Stir phase B into phase A. Heat phase C to approx. 80 ° C. and stir in phase A + B while homogenizing. Cool with stirring to about 40 ° C, add phase D and briefly homogenize.

The example can be repeated in each case with the polymers 2-7 according to the invention. A moisturizer with good properties is obtained in each case.

Example 54: Aerosol hair foam

A

2.00 cocotrimonium methsulfate

0.20 perfume oil

B

1, 60 polymer of Example 1 (solid) ad 100 dist. water

0.50 Poly (ethyl acrylate / methacrylic acid) (Luviflex Soft ^®)

0.10 aminomethylpropanol

0.20 Ceteareth-25

0.20 trimethylsilylamodimethicone, trideceth-10, cetrimonium chloride

0.10 PEG-25 PABA

0.20 hydroxyethylcellulose

0.20 PEG-8

0.20 Panthenol

15.00 alcohol

C

10.00 propane / butane 3.5 bar (20 ^° C.) production:

Mix phases A and B and fill with propellant.

The example can be repeated in each case with the polymers 2-7 according to the invention. In each case, an aerosol hair foam with good properties is obtained.

Example 55: pump mousse

A

2.00 cocotrimonium methosulfate q.s. perfume oil

C

7.00 Polyquaternium-46 (10% aqueous solution)

2.50 polymer from Example 1 (solid) ad 100 dist. Water 0.50 PEG-8

1, 00 Panthenol q.s. preservative

0.20 PEG-25 PABA (ethoxylated p-aminobenzoic acid)

production:

Mix the components of phase A. Add the components of phase B one after the other and dissolve clearly.

The example can be repeated in each case with the polymers 2-7 according to the invention. In each case a pump mousse with good properties is obtained.

Example 56: Aerosol foam

3.0 polymer from Example 1 (solid) ad 100 dist. water

5.00 PVP / VA copolymer (40% aqueous solution)

0.50 hydroxyethyl cetyldimonium phosphate

0.20 Ceteareth-25 0.40 Perfume oil PC 910.781 / Cremophor qs preservative

10.00 propane / butane 3.5 bar (20 ^° C.)

production:

Weigh everything together, stir until dissolved, then bottling.

The example can be repeated in each case with the polymers 2-7 according to the invention. In each case, an aerosol foam with good properties is obtained.

Example 57: Color Styling Mousse

A

2.00 cocotrimonium methosulfate q.s. perfume oil

B

6.50 polymer from Example 1 (solid) ad 100 dist. water

0.50 acrylate copolymer (Luvimer ^® 100 P, Fa. BASF)

0.10 aminomethylpropanol

0.20 Ceteareth-25

0.20 Panthenol

0.20 hydroxyethylcellulose

10,00 alcohol

0.08 Cl. 12245, Basic Red 76

0.05 Cl. 42510, Basic Violet 14

C

10.00 propane / butane 3.5 bar (20 ^° C.)

production:

Weigh everything together, stir until dissolved, then bottling. Only suitable for dark blond and brown hair!

The example can be repeated in each case with the polymers 2-7 according to the invention. In each case, a color styling mousse with good properties is obtained. Example 58: Pumped Hair Foam

A

1, 50 cocotrimonium methosulfate q.s. perfume oil

B

2.00 polymer from Example 1 (solid) ad 100 dist. water

C

0.46 aminomethylpropanol

4.00 PEG / PPG-25/25 dimethicone / acrylate copolymer q.s. preservative

production:

Mix phase A. Stir phase B into phase A. Add phase C and stir until dissolved.

The example can be repeated in each case with the polymers 2-7 according to the invention. It is obtained in each case a Pumphaarschaum with good properties.

Example 59: Aquawax

10 polymer from Example 1 (solid) ad 100 dist. Water q.s. Perfume oil q.s. hydrogenated castor oil PEG-40

0.10 diethyl phthalate

0.10 Cetearγlethylhexanoate

0.10 PEG-7 glyceryl cocoate

0.10 preservative

2.00 caprylic / capric triglyceride, acrylate copolymer

production:

Mix and homogenize everything. Stir for 15 minutes. The example can be repeated in each case with the polymers 2-7 according to the invention. In each case an aqua wax with good properties is obtained.

Example 60: Rinse-off Conditioner and Repair Treatment

A

0.20 Cetearyloctanoate

0.10 phytantriol

2.00 hydrogenated castor oil PEG-40

B q.s. perfume oil

2.00 cocotrimonium methosulfate

C ad 100 dist. water

D

2.00 Polyquaternium-16 (20% aqueous solution) 1, 0 Polymer from Example 1 (solid)

1, 00 dimethicone copolyol q.s. preservative

10,00 alcohol q.s. citric acid

production:

Mix phases A and B separately. Stir phase C into phase B.

The example can be repeated in each case with the polymers 2-7 according to the invention. In each case a rinse-off conditioner and repair treatment with good properties is obtained.

Example 61: hair conditioner

A

2.00 ceteareth-6, stearyl alcohol

1, 00 Ceteareth-25

6.00 Cetearyl alcohol

6.00 Cetearγ-octanoate 0.30 phytantriol

B

1, 0 polymer of Example 1 (solid) ad 100 dist. water

0.70 guar hydroxypropyltrimonium chloride

5.00 propylene glycol

2,00 Panthenol

0.30 imidazolidinyl urea

C

2,00 Cosi SiIk Soluble

0.20 perfume

0.50 phenoxyethanol

production:

Heat phases A and B separately to approx. 80 ° C. Homogenize phase B.

The example can be repeated in each case with the polymers 2-7 according to the invention. In each case a hair cure with good properties is obtained.

Example 62: Hair cocktail

A

0.40 acrylates / Cio ₃ oAlkyl acrylate crosspolymer

2.00 Dimethicon

3.00 cyclomethicone, dimethiconol

2.00 Phenyltrimethicone 2.00 Amodimethicone, Cetrimonium Chloride, Trideceth-10

0.50 dimethicone copolyol

1.00 macadamia nut oil (Ternifolia)

0.50 tocopheryl acetate

1, 00 PEG-40 Hydrogenated Castor OiI q.s. perfume oil

B

0.3 polymer of Example 1 (solid) ad 100 dist. Water 0.46 aminomethylpropanol 4.00 PEG / PPG-25/25 dimethicone / acrylate copolymer

production:

Mix the components of phase A. Solve phase B. Stir phase B into phase A while homogenizing.

The example can be repeated in each case with the polymers 2-7 according to the invention. In each case a hair cocktail with good properties is obtained.

Example 63: Perm

Well solution

A

0.20 cocamidopropyl betaine

0.20 polysorbate 20

1, 55 polymer from Example 1 (solid) ad 100 dist. water

0.20 disodium EDTA

0.20 hydroxyethylcellulose

B

8.00 thioglycolic acid

C

11, 00 ammonium hydroxide

D

5.00 ammonium carbonate

production:

Weigh in the components of phase A and dissolve clearly. Stir phase B into phase A.

The example can be repeated in each case with the polymers 2-7 according to the invention. In each case, a well solution with good properties is obtained.

Example 64: Fixation: A

1, 00 PEG-40 Hydrogenated Castor OiI

0.20 perfume oil ad 100 dist. water

B

0.20 cocamidopropyl betaine

0.20 Ceteareth-25 2.5 Polymer from Example 1 (solid) q.s. preservative

C

2.30 hydrogen peroxide

D q.s. phosphoric acid

production:

Solubilize phase A. Add the components of phase B one after the other and dissolve clearly.

The example can be repeated in each case with the polymers 2-7 according to the invention. In each case, a fixation with good properties is obtained.

Example 65: dark brown permanent hair color (oxidation hair color)

A

0.20 sodium sulfite

0.05 disodium EDTA

0.20 p-phenylenediamine

0.30 resorcinol

0.20 4-amino-2-hydroxytoluene

0.10m aminophenol

1, 50 oleyl alcohol

4.50 propylene glycol

2.30 Sodium C ₁₂ - ₁₅ Pareth-15 Sulfonates

20.00 oleic acid ad 100 dist. water B

1, 0 polymer from Example 1 (solid)

13.70 ammonium hydroxide 6.00 i-propanol q.s. Perfume

production:

Solubilize phase A. Add the components of phase B one after the other and mix.

The example can be repeated in each case with the polymers 2-7 according to the invention. In each case, a dark brown permanent hair color (oxidation hair color) having good properties is obtained.

Example 66: Developer emulsion (pH 3 -4)

3.00 hexadecyl alcohol

1, 0 polymer of Example 1 (solid) ad 100 dist. water

1, 00 Ceteareth-20

1, 00 sodium C ₁₂ - ₁₅ pareth-15 sulfonates

6.00 hydrogen peroxide

0.50 phosphoric acid

0.01 acetanilide

production:

Add the components one after the other and mix.

The example can be repeated in each case with the polymers 2-7 according to the invention. In each case, a developer emulsion (pH 3 - 4) having good properties is obtained.

Example 67: light brown semi-permanent hair color

10.00 cocodiethanolamide

4.00 sodium dodecylbenzylsulfonate, 50% 1, 0 polymer from Example 1 (solid) ad 100 dist. water

6.00 C _9- i ₁ Pareth-3

2.50 sodium lauryl sulfate

0.40 2-nitro-p-phenylenediamine

0.20 HC Red No.3

0.20 HC Yellow No.2

production:

Add the components one after the other and mix.

The example can be repeated in each case with the polymers 2-7 according to the invention. In each case, a light brown semi-permanent hair color with good properties is obtained.

Example 68: shampoo

30.00 Sodium Laureth Sulfate

6.00 Sodium Cocoamphoacetate

6.00 Cocamidopropyl betaine

3.00 Sodium Laureth Sulfate, Glycol Distearate, Cocamide

MEA, Laureth-10

1, 0 polymer from Example 1 (solid)

2.00 Dimethicon q.s. Perfume q.s. Preservative q.s. citric acid

1, 00 sodium chloride ad 100 dist. water

production:

Weigh in and release components. Adjust pH to 6 to 7.

The example can be repeated in each case with the polymers 2-7 according to the invention. In each case a shampoo with good properties is obtained.

Example 69: shampoo

30.00 Sodium Laureth Sulfate 6.00 Sodium Cocoamphoacetate

6.00 Cocamidopropyl betaine

3.00 Sodium Laureth Sulfate, Glycol

Distearates, Cocamide MEA, Laureth-10

1, 0 polymer from Example 1 (solid)

2.00 Amodimethicone q.s. Perfume q.s. Preservative q.s. citric acid

1, 00 sodium chloride ad 100 dist. water

production:

Weigh in and release components. Adjust pH to 6 to 7.

The example can be repeated in each case with the polymers 2-7 according to the invention. In each case a shampoo with good properties is obtained.

Example 70: Shampoo

40.00 Sodium Laureth Sulfate

10.00 Cocamidopropyl betaine

3.00 Sodium Laureth Sulfate, Glycol

Distearates, Cocamide MEA, Laureth-10

1, 0 polymer from Example 1 (solid)

2.00 Dow Corning 3052 q.s. Perfume q.s. Preservative q.s. citric acid

2.00 Cocamido DEA ad 100 dist. water

production:

Weigh in and release components. Adjust pH to 6 to 7.

The example can be repeated in each case with the polymers 2-7 according to the invention. In each case a shampoo with good properties is obtained. Example 71: Anti-dandruff shampoo

40.00 Sodium Laureth Sulfate

10.00 Cocamidopropyl betaine

10.00 Disodium Laureth Sulfosuccinate

2.50 Sodium Laureth Sulfate, Glycol Distearate, Cocamide MEA, Laureth-10

1, 0 polymer from Example 1 (solid)

0.50 Climbazole q.s. Perfume q.s. preservative

0.50 sodium chloride ad 100 dist. water

Production: weigh in and release components. Adjust pH to 6 to 7.

The example can be repeated in each case with the polymers 2-7 according to the invention. In each case an anti-dandruff shampoo with good properties is obtained.

Example 72: shampoo

25.00 Sodium Laureth Sulfate

5.00 Cocamidopropyl betaine 2.50 Sodium Laureth Sulfate, Glycol Distearate, Cocamide MEA, Laureth-10

1, 0 Polymer from Example 1 (solid) q.s. Perfume q.s. preservative

2.00 Cocamido DEA ad 100 dist. water

production:

Weigh in and release components. Adjust pH to 6 to 7.

The example can be repeated in each case with the polymers 2-7 according to the invention. In each case a shampoo with good properties is obtained. Example 73: shampoo

20.00 Ammonium Laureth Sulfate

15.00 Ammonium Lauryl Sulfate

5.00 cocamidopropyl betaine

2.50 Sodium Laureth Sulfate, Glycol Distearate. Cocamide

MEA, Laureth-10

1, 0 Polymer from Example 1 (solid) q.s. Perfume q.s. preservative

0.50 sodium chloride ad 100 dist. water

production:

Weigh in and release components. Adjust pH to 6 to 7.

The example can be repeated in each case with the polymers 2-7 according to the invention. In each case a shampoo with good properties is obtained.

Example 74: Clear shower gel

40.00 Sodium Laureth Sulfate

5.00 decylglucoside

5.00 cocamidopropyl betaine

1, 0 polymer from Example 1 (solid)

1, 00 Panthenol q.s. Perfume q.s. Preservative q.s. citric acid

2.00 sodium chloride ad 100 dist. water

production:

Weigh in and release components. Adjust pH to 6 to 7.

The example can be repeated in each case with the polymers 2-7 according to the invention. It will receive a clear shower gel with good properties. Example 75: Shampoo

12,00 Sodium Laureth Sulfate

1, 50 decylglucoside 2.50 cocamidopropyl betaine

5.00 Coco-Glucoside Glyceryl Oleate

2.00 Sodium Laureth Sulfate, Glycol Distearate. Cocamide MEA, Laureth-10

1, 0 Polymer from Example 1 (solid) q.s. Preservative q.s. Sunset Yellow C.I. 15 985 q.s. Perfume

1, 00 sodium chloride ad 100 dist. water

production:

Weigh in and release components. Adjust pH to 6 to 7.

The example can be repeated in each case with the polymers 2-7 according to the invention. In each case a shampoo with good properties is obtained.

Example 76: Shampoo

A

40.00 Sodium Laureth Sulfate

5.00 Sodium Ci ₂ -i ₅ Pareth-15 Sulfonates

5.00 decylglucoside q.s. Perfume

0.10 phytantriol

B

1, 0 polymer of Example 1 (solid) ad 100 dist. water

1, 00 Panthenol q.s. preservative

1, 00 Laureth-3 q.s. citric acid

2.00 sodium chloride production:

Weigh and solve phase A components. Adjust pH to 6 to 7. Add phase B and mix.

The example can be repeated in each case with the polymers 2-7 according to the invention. In each case a shampoo with good properties is obtained.

Claims

124Patentansprüche

1. Cosmetic preparation containing at least one polymer A, which contains a) methyl methacrylate, b) methacrylic acid, c) acrylic acid, d) if desired at least one compound having at least two free-radically polymerizable, olefinically unsaturated double bonds and e) optionally further copolymerized olefinically unsaturated compounds, with the proviso that the amount by weight of component b) is at least equal to the amount by weight of component c).

2. Cosmetic preparation according to claim 1, wherein polymer A a) 50-85 wt .-% methyl methacrylate, b) 1-30 wt .-% methacrylic acid, c) 1-20 wt .-% acrylic acid, d) 0-5 Wt .-% of at least one compound having at least two radic kaiisch polymerizable olefinically unsaturated double bonds e) 0-30 wt .-% of further olefinically unsaturated compounds in copolymerized form, with the proviso that, calculated as wt .-%, the amount of Component b) is at least equal to the amount of component c) and that the amounts of components a) to e) add up to 100 wt .-%.

3. Cosmetic preparation according to claims 1 or 2, wherein polymer A a) 65-80 wt .-% methyl methacrylate, b) 5-25 wt .-% methacrylic acid, c) 3-15 wt .-% acrylic acid, d) 0-4 wt .-% of at least one compound having at least two radically polymerizable, olefinically unsaturated double bonds e) 0-20 wt .-% of further olefinically unsaturated compounds in copolymerized form.

4. Cosmetic preparation according to one of claims 1 to 3, wherein polymer A a) 70-80 wt .-% methyl methacrylate, b) 10-20 wt .-% methacrylic acid, c) 5-10 wt .-% acrylic acid, 125 d) 0.5-3 wt .-% of at least one compound having at least two free-radically polymerizable, olefinically unsaturated double bonds, e) 0-14.5 wt .-% of further olefinically unsaturated compounds in copolymerized form.

5. Cosmetic preparation according to one of claims 1 to 4, wherein the weight ratio of b) to c) at least 1, 2: 1.

6. Cosmetic preparation according to one of claims 1 to 5, wherein polymer

A has a K value in the range of 25 to 45.

7. Cosmetic preparation according to one of claims 1 to 6, wherein the proportion of volatile organic components is at most 55 wt .-%, based on the cosmetic preparation.

8. Cosmetic preparation according to one of claims 1 to 7, wherein the preparation further comprises at least one cosmetically acceptable carrier B), which is selected from i) water-miscible organic solvents, preferably C ₂ -

C ₎ alkanols, particularly preferably ethanol, ii) oils, fats, waxes, iii) of ii) various esters of C ₆ -C ₃₀ monocarboxylic acids with mono-, di- or trihydric alcohols, iv) saturated acyclic and cyclic hydrocarbons, v) fatty acids, vi) fatty alcohols, vii) propellants (propellant gases) and viii) mixtures thereof.

A cosmetic preparation according to any one of claims 1 to 8 in the form of a spray product, wherein the preparation is either in combination with a mechanical pump spray device or in combination with at least one propellant selected from the group consisting of propane, butane, dimethyl ether, fluorinated hydrocarbons and mixtures thereof is present.

10. A polymer as defined in any one of claims 1 to 8.

11. Use of polymer A according to claim 10 in cosmetic preparations.