WO2001078661A2 - Aerosol foam for treating hair - Google Patents
Aerosol foam for treating hair Download PDFInfo
- Publication number
- WO2001078661A2 WO2001078661A2 PCT/EP2001/003799 EP0103799W WO0178661A2 WO 2001078661 A2 WO2001078661 A2 WO 2001078661A2 EP 0103799 W EP0103799 W EP 0103799W WO 0178661 A2 WO0178661 A2 WO 0178661A2
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- WO
- WIPO (PCT)
- Prior art keywords
- aerosol
- aerosol foam
- hair
- foam according
- cationic
- Prior art date
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Classifications
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/02—Cosmetics or similar toiletry preparations characterised by special physical form
- A61K8/04—Dispersions; Emulsions
- A61K8/046—Aerosols; Foams
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
- A61K8/81—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
- A61K8/817—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a single or double bond to nitrogen or by a heterocyclic ring containing nitrogen; Compositions or derivatives of such polymers, e.g. vinylimidazol, vinylcaprolactame, allylamines (Polyquaternium 6)
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
- A61K8/81—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
- A61K8/817—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a single or double bond to nitrogen or by a heterocyclic ring containing nitrogen; Compositions or derivatives of such polymers, e.g. vinylimidazol, vinylcaprolactame, allylamines (Polyquaternium 6)
- A61K8/8182—Copolymers of vinyl-pyrrolidones. Compositions of derivatives of such polymers
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
- A61K8/84—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions otherwise than those involving only carbon-carbon unsaturated bonds
- A61K8/89—Polysiloxanes
- A61K8/891—Polysiloxanes saturated, e.g. dimethicone, phenyl trimethicone, C24-C28 methicone or stearyl dimethicone
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q5/00—Preparations for care of the hair
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K2800/00—Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
- A61K2800/40—Chemical, physico-chemical or functional or structural properties of particular ingredients
- A61K2800/54—Polymers characterized by specific structures/properties
- A61K2800/542—Polymers characterized by specific structures/properties characterized by the charge
- A61K2800/5426—Polymers characterized by specific structures/properties characterized by the charge cationic
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K2800/00—Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
- A61K2800/40—Chemical, physico-chemical or functional or structural properties of particular ingredients
- A61K2800/54—Polymers characterized by specific structures/properties
- A61K2800/542—Polymers characterized by specific structures/properties characterized by the charge
- A61K2800/5428—Polymers characterized by specific structures/properties characterized by the charge amphoteric or zwitterionic
Definitions
- the invention relates to an aerosol foam for hair treatment containing at least one cationic, amphoteric or zwitterionic polymer, at least one surfactant, at least one defoamer, an aqueous or aqueous-alcoholic solvent system and at least one aerosol propellant.
- the defoamer is preferably a silicone antifoam emulsion which contains physiologically indifferent active components based on polydimethylsiloxane / silica.
- Aerosol foams for hair treatment are known and generally consist of hair-setting or hair-care substances, foaming agents and propellant gases and a suitable water-based solvent base.
- Various demands are placed on the quality of such aerosol foams, which can be roughly divided into two groups.
- One group of quality requirements relates to the quality of the foam, ie the nature of the foam. These include, for example, the fine or coarse pores, the compactness, the temporal stability of the foam, the incorporability and distributability on the hair, etc.
- the second group of quality requirements relates to the effects that the foam has on the hair after incorporation into the hair , ie the hair care properties such as, for example, the handle of the hair when wet and dry, the combability, the strengthening, the stress on the hair, etc.
- the problem with the optimization of aerosol foams is that although the addition of special active ingredients can improve some quality requirements, for example the foam quality, this is bought with a deterioration in other quality requirements, for example the hair-care properties.
- the object was therefore to improve the foam quality of aerosol foams for hair treatment, the hair care properties not being impaired at the same time, but ideally also being improved.
- the subject of the invention is therefore an aerosol foam for hair treatment containing
- the polymer (A) is contained in the agent according to the invention preferably in an amount of 0.01 to 20, particularly preferably from 0.02 to 10, very particularly preferably from 0.1 to 5 percent by weight.
- Suitable polymers (A) are those which, owing to cationic or cationizable groups, in particular primary, secondary, tertiary or preferably quaternary amine groups, have a substantivity to human hair.
- Suitable polymers (A) are selected from polymers with cationic or cationizable groups, polymeric silicone compounds with cationic or cationizable groups and cationically derivatized proteins or protein hydrolyzates.
- the suitable cationic polymers are hair-setting and / or hair-conditioning polymers.
- Suitable polymers of component (A) preferably contain quaternary amine groups.
- the cationic polymers can be homo- or copolymers, the quaternary nitrogen groups being contained either in the polymer chain or preferably as a substituent on one or more of the monomers.
- the monomers containing ammonium groups can be copolymerized with non-cationic monomers.
- Suitable cationic monomers are unsaturated, free-radically polymerizable compounds which carry at least one cationic group, in particular ammonium-substituted vinyl monomers such as, for example, trialkylmethacryloxyalkylammonium, trialkylacryloxyalkylammonium, dialkyldiallylammonium and quaternary vinylammonium monomers containing cyclic, cationic nitrogenous substances Groups such as pyridinium, imidazolium or quaternary pyrrolidones, for example alkylvinylimidazolium, alkylvinylpyridinium, or alylvinylpyrrolidone salts.
- the alkyl groups of these monomers are preferably lower alkyl groups such as, for example, Cl to C7 alkyl groups, particularly preferably Cl to C3 alkyl groups.
- the monomers containing ammonium groups can be copolymerized with non-cationic monomers.
- Suitable non-cationic comonomers are, for example, acrylamide, methacrylamide, alkyl and dialkyl acrylamide, alkyl and dialkyl methacrylamide, alkyl acrylate, alkyl methacrylate, vinyl caprolactone, vinyl caprolactam, vinyl pyrrolidone, vinyl ester, e.g. Vinyl acetate, vinyl alcohol, propylene glycol or ethylene glycol, the alkyl groups of these monomers preferably being Cl to C7 alkyl groups, particularly preferably Cl to C3 alkyl groups.
- Suitable polymers with quaternary amine groups are, for example, the polymers described in the CTFA Cosmetic Ingredient Dictionary under the names Polyquaternium, such as dimethyldiallylammonium chloride / acrylic acid copolymer (Polyquaternium-22), methylvinylimidazolium chloride / vinylpyrrolidone copolymer (Polyquaternium-16) or quaternized vinylpyramethyl-acrylate / vinylpyramethyl-copolymerized Polyquaternium-11) and quaternary silicone polymers or oligomers such as silicone polymers with quaternary end groups (Quaternium-80).
- Polyquaternium such as dimethyldiallylammonium chloride / acrylic acid copolymer (Polyquaternium-22), methylvinylimidazolium chloride / vinylpyrrolidone copolymer (Polyquaternium-16) or quaternized vinylpyramethyl-acrylate / vinylpyramethyl-copolymerized Polyquaternium-11
- Other cationic polymers include those from BASF,
- Gaffix VC 713 sold terpolymer of vinyl pyrrolidone, dimethylaminoethyl methacrylate and vinyl caprolactam and that from Gaf under the
- Suitable cationic polymers derived from natural polymers are cationic derivatives of polysaccharides, for example cationic derivatives of cellulose, starch or guar. Chitosan and chitosan derivatives are also suitable.
- Cationic polysaccharides have the general formula (I)
- G is an anhydroglucose residue, e.g. starch or cellulose anhydroglucose;
- B is a divalent Linking group, for example alkylene, oxyalkylene, polyoxyalkylene or hydroxyalkylene;
- R a , R b and R c are independently of one another alkyl, aryl, alkylaryl, arylalkyl, alkoxyalkyl or alkoxyaryl each having up to 18 C atoms, the total number of C atoms in R a , R b and R c preferably being a maximum of 20 is;
- X is a common counter anion, for example a halogen, acetate, phosphate, nitrate or alkyl sulfate, preferably a chloride.
- a cationic cellulose is sold under the name Polymer JR by Amerchol and has the INCI name Polyquaternium-10.
- Another cationic cellulose has the INCI name Polyquaternium-24 and is sold under the trade name Polymer LM-200 by
- a suitable cationic guar derivative is sold under the trade name Jaguar R and has the INCI name guar hydroxypropyltrimonium chloride.
- Particularly preferred cationic substances are chitosan, chitosan salts and chitosan derivatives.
- the chitosans to be used according to the invention are completely or partially deacetylated chitins.
- the production of chitosan is preferably based on the chitin contained in the shell remains of crustaceans, which is available in large quantities as a cheap and natural raw material.
- the molecular weight of the chitosan can be distributed over a broad spectrum, for example from 20,000 to about 5 million g / mol.
- a low molecular weight chitosan with a molecular weight of 30,000 to 70,000 g / mol is suitable.
- the molecular weight is preferably above 100,000 g / mol, particularly preferably from 200,000 to 700,000 g / mol.
- the degree of deacetylation is preferably 10 to 99%, particularly preferably 60 to 99%.
- a suitable chitosan is, for example, from the company Kyowa Oil & Fat, Japan, under the trade name
- Flonac distributed. It has a molecular weight of 300,000 to 700,000 g / mol and is 70 to 80% deacetylated.
- a preferred chitosan salt is chitosonium pyrrolidone carboxylate, which is sold, for example, under the name Kytamer PC by Amerchol, USA.
- the chitosan contained has a molecular weight of approx. 200,000 to 300,000 g / mol and is 70 to 85% deacetylated.
- Quaternized, alkylated or hydroxyalkylated derivatives, for example hydroxyethyl, hydroxypropyl or hydroxybutyl chitosan, are suitable as chitosan derivatives.
- the chitosans or chitosan derivatives are preferably in neutralized or partially neutralized form.
- the degree of neutralization for the chitosan or the chitosan derivative is preferably at least 50%, particularly preferably between 70 and 100%, based on the number of "free base groups.
- Tion medium as Neutralisa- principle all cosmetically compatible inorganic or organic acids can be used such as formic acid , Tartaric acid, malic acid, lactic acid, citric acid, pyrrolidone carboxylic acid, hydrochloric acid and others, of which pyrrolidone carboxylic acid is particularly preferred.
- Preferred polymers are those which have sufficient solubility in aqueous or aqueous-alcoholic solvent systems in order to be able to medium in completely dissolved form.
- the cationic charge density is preferably 1 to 7 meq / g.
- Suitable cationic silicone compounds preferably have either at least one amino group or at least one ammonium group.
- Suitable silicone polymers with amino groups are known under the INCI name Amodimethicone. These are polydimethylsiloxanes with aminoalkyl groups. The aminoalkyl groups can be side or terminal.
- Suitable aminosilicones are those of the general formula (II)
- R 1 , R 2 , R 7 and R 8 are independently the same or different and are Cl- to CIO-alkyl, phenyl, hydroxy, hydrogen, Cl- to ClO-alkoxy or acetoxy, preferably C1-C4-alkyl, particularly preferred Methyl;
- R 3 and R 9 are independently the same or different and are - (CH 2 ) a -NH 2 with a equal to 1 to 6, Cl to CIO alkyl, phenyl, hydroxy, hydrogen, Cl to ClO alkoxy or acetoxy , preferably C1-C4-alkyl, particularly preferably methyl;
- R 4 , R 5 and R 6 are independently the same or different and are hydrogen, Cl- to C20-hydrocarbon, which can contain O and N atoms, preferably Cl- to CIO-alkyl or phenyl, particularly preferably Cl- bis C4 alkyl, especially methyl;
- Q is -A-NR ⁇ R 11 , or -AN + R 10 R 1X R 12 where A is a divalent Cl to C20 alkylene linking group, which can also contain 0 and N atoms and OH groups, and R 10 , R 11 and R 12 are independently the same or different and are hydrogen, Cl to C22 hydrocarbon, preferably Cl to C-4 alkyl or Phenyl mean.
- Preferred radicals for Q are
- R 13 is a Cl to C22 alkyl radical, which may also have OH groups.
- X represents a number between 1 and 10,000, preferably between 1 and 1,000;
- Y represents a number between 1 and 500, preferably between 1 and 50.
- the molecular weight of the aminosilicones is preferably between 500 and 100,000.
- the amine content (meq / g) is preferably in the range from 0.05 to 2.3, particularly preferably from 0.1 to 0.5.
- Suitable silicone polymers with two terminal quaternary ammonium groups are known under the INCI name Quaternium-80. These are dimethylsiloxanes with two terminal aminoalkyl groups. Suitable quaternary aminosilicones are those of the general formula (III)
- R 13 is a Cl to C22 alkyl radical, which may also have OH groups;
- R 1 , R 2 , R 4 and R 5 have the same meaning as given above for formula (II) and are preferably methyl;
- R 14 , R 15 and R 16 independently of one another are C 1 to C 22 alkyl radicals which may contain hydroxyl groups and where preferably at least one of the radicals has at least 10 C atoms and the remaining radicals have 1 to 4 C atoms;
- n is a number from 0 to 200, preferably 10 to 100.
- Such diquaternary polydimethylsiloxanes are sold by GOLDSCHMIDT / Germany under the trade names Abil ® Quat 3270, 3272 and 3274.
- cationic, hair-care compounds are cationically modified protein derivatives or cationically modified protein hydrolyzates and are known, for example, under the INCI names lauryldimonium hydroxypropyl hydrolyzed wheat protein, lauryldimonium hydroxypropyl hydrolyzed casein, lauryldimonium hydroxypropyl hydrolyzed collagen, lauryldimonium hydroxypropyl, and lauryldimonium hydroxypropyl , Lauryidimonium hydroxypropyl or hydroxypropyltrimonium Hydrolyzed Soy protein Hydrolyzed Wheat, hydroxypropyltrimonium Hydrolyzed casein, hydroxypropyltrimonium Hydrolyz "ed collagen, hydroxypropyltrimonium Hydrolyzed keratin, hydroxypropyltrimonium Hydrolyzed Rice Bran protein, hydroxypropyltrimonium Hydrolyzed Silk, hydroxypropyltrimonium Hydrolyzed Soy protein, Hydro
- Suitable cationically derivatized protein hydrolyzates are mixtures of substances which are obtained, for example, by reacting alkaline, acidic or enzymatically hydrolyzed proteins with glycidyltrialkylammonium salts or 3-halo-2-hydroxypropyltrialkylammonium salts can be obtained.
- Proteins that serve as starting materials for the protein hydrolyzates can be of both vegetable and animal origin. Common starting materials are, for example, keratin, collagen, elastin, soy protein, rice protein, milk protein,
- the hydrolysis produces mixtures of substances with molecular weights in the range from approximately 100 to approximately 50,000. Usual average molecular weights are in the range from about 500 to about 1000.
- the cationically derivatized protein hydrolyzates advantageously contain one or two long C8 to C22 alkyl chains and correspondingly two or a short Cl to C4 alkyl chain. Compounds containing a long alkyl chain are preferred.
- Suitable amphoteric polymers are those which, in addition to cationic or cationizable basic groups, in particular primary, secondary, tertiary or quaternary amine groups, contain anionic or anionizable acidic groups as further functional groups.
- Examples of these are copolymers formed from alkyl acrylamide (in particular octylacrylamide), alkylaminoalkyl methacrylate (in particular t-butylaminoethyl methacrylate) and two or more monomers consisting of acrylic acid, methacrylic acid or their esters (INCI name: octylacrylamides / acrylates / butylaminoethyl) Methacrylate copolymer), such as
- amphomer ® LV-71 from NATIONAL STARCH, USA.
- Further suitable amphoteric polymers are copolymers which are formed from at least one first type of monomer which has quaternary amine groups and at least one second type of monomer which has acid groups.
- copolymers examples include copolymers of acrylic acid, methyl acrylate and methacrylamidopropyltrimethylammonium chloride (INCI name: Polyquaternium-47), as are marketed, for example, by the company Calgon under the trade name Merquat "2001, copolymers of acrylamidopropyltrimethylammonium chloride and acrylates, as are used, for example, by the Stockhausen company are available under the trade name W 37194 or copolymers of acrylamide, acrylamidopropyltrimethylammonium chloride, 2-amidopropylacrylamide sulfonate and dirnethylaminopropylamine (INCI name: Polyquaternium-43), such as those from Societe Francaise
- Bozequat 4000 Polymers with monomers bearing betaine groups, such as e.g. Copolymers of methacryloylethylbetaine and two or more monomers of acrylic acid or their simple esters, known under the INCI name Methacryloyl Ethyl Betaine / Acrylates Copolymer.
- the surfactant (B) is contained in the agent according to the invention preferably in an amount of 0.01 to 15, particularly preferably 0.05 to 10 percent by weight.
- Suitable surfactants have emulsifying, solubilizing, foam-forming or foam-enhancing properties and are preferably nonionic.
- non-ionic surfactants are suitable for the hair treatment composition according to the invention if they have an HLB value of at most 20, preferably from 5 to 18.
- Ethoxylated surfactants are preferred, the number of ethylene oxide units being between 1 and 1000, preferably between 1 and 300, particularly preferably between 1 and 15.
- Fatty acid glyceride ethoxylates, fatty alcohol ethoxylates, fatty amine ethoxylates, fatty acid alkanolamide ethoxylates and fatty acid ester ethoxylates each with 1 to 50 ethylene oxide units are preferred.
- suitable fatty alcohol ethoxylates are oxyethylated lauryl, tetradecyl, cetyl, oleyl or stearyl alcohol, which can be used alone or in a mixture, and fatty alcohols of oxyethylated lanolin or oxyethylated lanolin.
- the ethoxylated fatty alcohols which are marketed under the type name Dehydol by Henkel or under the type name Brij ® by ICI Surfactants, are also suitable for the hair treatment composition according to the invention.
- diglyceride ethoxylates such as that from ICI are particularly worth mentioning
- nonionic surfactants sold under the name Rewoderm ® LI.
- Preferred nonionic surfactants are ethoxylated FettTexrezuckerester, in particular ethoxylated sorbitan fatty acid esters known as polysorbates, but not ethoxylated surfactants, such as the FettTexrezuckerester, sold by ICI Surfactants under the trade name Tween and Arlacel ®, as well as the alkyl polyglycosides, of the company
- the defoamer (C) is preferably present in the aerosol hair foam according to the invention in an amount of 0.001 to 0.5, particularly preferably 0.005 to 0.1% by weight.
- Non-organic defoamers are preferred, especially those based on physiologically indifferent active components such as polydimethylsiloxane / silica. Such active ingredients are known under the
- Simethicone This is a mixture of dimethicones (polydimethylsiloxanes) with an average chain length of 200 to 350 dimethylsiloxane units and hydrated silica. They can be used in the form of silicone antifoam emulsions. These are aqueous emulsions of simethicones.
- the agent according to the invention is confectioned in an aqueous or in an aqueous-alcoholic medium with preferably at least 10 percent by weight of water. kidney.
- the solvent system is preferably contained in an amount of 50 to 98, particularly preferably 75 to 95 percent by weight.
- the lower alcohols with 1 to 4 carbon atoms usually used for cosmetic purposes, such as ethanol and isopropanol, can be included as alcohols.
- the agent according to the invention can be present in a pH range from 2.0 to 9.5. The pH range between 3.5 and 8 is particularly preferred.
- Organic solvents or a mixture of solvents with a boiling point below 400 ° C. can be present as additional co-solvents in an amount of 0.1 to 15, preferably 1 to 10 percent by weight.
- Unbranched or branched hydrocarbons such as pentane, hexane, isopentane and cyclic hydrocarbons such as cyclopentane and cyclohexane are particularly suitable as additional co-solvents.
- Other particularly preferred water-soluble solvents are glycerol, ethylene glycol and propylene glycol.
- the blowing agent (E) is preferably present in the aerosol hair foam according to the invention in an amount of 1 to 20, particularly preferably 2 to 10 percent by weight.
- blowing agents are, for example, lower alkanes, such as n-butane, i-butane, propane, butane, or also their mixtures, and also dimethyl ether or fluorocarbons such as F 152a (1,1-difluoroethane) or F 134 (tetrafluoroethane) and further suitable at the pressures under consideration gaseous blowing agents, such as N 2 , N 2 0 and C0 2, as well as mixtures of the blowing agents mentioned above.
- the agent according to the invention additionally contains 0.01 to 15 percent by weight, preferably 0.5 to 10 percent by weight, of at least one synthetic or natural nonionic film-forming polymer.
- Particularly preferred are those polymers which have sufficient solubility in water or water / alcohol mixtures to be present in the agent according to the invention in completely dissolved form.
- film-forming polymers are understood to mean those polymers which, when used in 0.01 to 5% aqueous, alcoholic or aqueous-alcoholic solution, are able to deposit a polymer film on the hair.
- Suitable synthetic, nonionic film-forming, hair-fixing polymers are homopolymers or copolymers which are composed of at least one of the following monomers: vinylpyrrolidone, vinylcaprolactam, vinyl esters such as e.g. Vinyl acetate, vinyl alcohol, acrylamide, methacrylamide, alkyl and dialkylacrylamide, alkyl and dialkyl methacrylamide, alkyl acrylate, alkyl methacrylate, propylene glycol or ethylene glycol, the alkyl groups of these monomers preferably Cl to C7 alkyl groups, particularly preferably Cl to bis C3 are alkyl groups.
- Homopolymers of vinyl caprolactam, vinyl pyrrolidone or N-vinyl formamide are suitable, for example.
- Other suitable synthetic film-forming, non-ionic, hair-fixing polymers are, for example, copolymers of vinyl pyrrolidone and vinyl acetate, terpolymers of vinyl pyrrolidone, vinyl acetate and vinyl propionate, polyacrylamides, for example under the trade names Akypomine "P 191 sold by the company CHEM-Y, Emmerich or Sepigel ® 305 by the company SEPPIC; polyvinyl alcohols, for example, under the
- Suitable natural film-forming polymers are e.g. Cellulose derivatives, e.g. Hydroxypropyl cellulose with a molecular weight of 30,000 to 50,000 g / mol, which is sold, for example, under the trade name Nisso Sl ® by Lehmann & Voss, Hamburg.
- the agent according to the invention can furthermore contain the additional ingredients customary for hair treatment agents, for example perfume oils in an amount of 0.01 to 0.5 percent by weight; Opacifiers, such as ethylene glycol distearate, in an amount of about 0.2 to 5.0 percent by weight; Preservatives such as parabens in an amount of 0.01 to 1.0 percent by weight; Buffer substances such as sodium citrate or sodium phosphate in an amount of 0.1 to 1.0 percent by weight; Care substances, such as plant and herbal extracts, protein and silk hydrolyzates, lanolin derivatives, in an amount of 0.1 to 5 percent by weight; physiologically compatible silicone derivatives, such as volatile or non-volatile silicone oils or highly molecular siloxane polymers in an amount of 0.05 to 20% by weight; Light stabilizers, antioxidants, radical scavengers, antidandruff agents, in an amount of about 0.01 to 2% by weight; direct hair dyes, hair dyes that are developed oxidatively, oxidizing agents, reducing agents,
- the aerosol foam according to the invention is filled in a pressure-resistant aerosol packaging which is provided with an aerosol foam head.
- a foam forms which can be worked into the hair particularly easily and which breaks down particularly quickly when it is worked into the hair.
- the cosmetic agent according to the invention is applied by applying and incorporating it in an amount sufficient to achieve the desired hair-care or hair-fixing effect on damp, towel-dried hair and leaving it in the hair without rinsing. Then the hairstyle can be shaped in the usual way or the hair can be inserted and finally blow-dried. But it is also possible to use the product directly on dry hair.
- a foam that breaks down very quickly on the hair can be obtained.
- the care properties are not impaired by the very small amount used (for example 0.01-0.5% by weight) but even improved, especially the wet grip, the combability, the dry grip and the strain on dry hair.
- the mixture of active ingredients was filled in a ratio of 92: 8 with propane / n-butane 4.8 bar as propellant in an aerosol can with a foam valve.
- Pattern 1E has an improved foam quality compared to pattern IV, the foam breaks down faster and is less stable and compact.
- the hair treated with pattern 1E has a better grip on damp hair than the hair treated with pattern IV.
- the hair feels lighter and less greasy.
- the hair treated with sample 1E has better combability than the hair treated with sample IV.
- the hair treated with pattern 1E has a better grip on dry hair than the hair treated with pattern IV.
- the hair feels lighter and less oily.
- the hair treated with sample 1E has a lower load than the hair treated with sample IV.
- the mixture of active ingredients was filled in a ratio of 94: 6 with propane / n-butane 4.8 bar as propellant in an aerosol can with a foam valve.
- the mixture of active ingredients was filled in a ratio of 92: 8 with propane / n-butane 4.8 bar as propellant in an aerosol can with a foam valve.
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Abstract
Description
Beschreibung description
Aerosolschäum zur HaarbehandlungAerosol foam for hair treatment
Gegenstand der Erfindung ist ein Aerosolschaum zur Haarbehandlung mit einem Gehalt an mindestens einem kationischen, amphoteren oder zwitterionischen Polymer, mindestens einem Tensid, mindestens einem Entschäumer, einem wässrigen oder wässrig-alkoholischen Lösungs- mittelsystem und mindestens einem Aerosol-Treibmittel. Bei dem Entschäumer handelt es sich vorzugsweise um eine Silicon-Antischaumemulsion, welche physiologisch indifferente Wirkkomponenten auf Basis von Polydi- methylsiloxan/Silica enthält.The invention relates to an aerosol foam for hair treatment containing at least one cationic, amphoteric or zwitterionic polymer, at least one surfactant, at least one defoamer, an aqueous or aqueous-alcoholic solvent system and at least one aerosol propellant. The defoamer is preferably a silicone antifoam emulsion which contains physiologically indifferent active components based on polydimethylsiloxane / silica.
Aerosolschäume zur Haarbehandlung sind bekannt und bestehen in der Regel aus haarfestigenden oder haarpflegenden Substanzen, Schaumbildnern und Treibgasen sowie einer geeigneten wasserhaltigen Lösungsmittelbasis. An die Qualität von derartigen Aerosolschäumen werden verschiedene Anforderungen gestellt, die grob in zwei Gruppen aufgeteilt werden können. Die eine Gruppe von Qualitätsanforderungen betrifft die Schaumqualität, d.h. die Beschaffenheit des Schaumes. Hierzu gehören etwa die Fein- oder Grobporigkeit, die Kompaktheit, die zeitliche, Stabilität des Schaumes, die Einarbeitbarkeit und Verteilbarkeit auf dem Haar etc.. Die zweite Gruppe von Qualitätsanforderungen betrifft die Wirkungen, die der Schaum nach Einarbeitung in das Haar auf dem Haar hervorruft, d.h. die haarpflegenden Eigenschaften wie z.B. der Griff des Haares im feuchten und trockenen Zustand, die Kämmbarkeit, die Festigung, die Belastung des Haares etc.. Bei der Optimierung von Aerosolschäumen besteht das Problem, dass zwar durch Zusatz spezieller Wirkstoffe eine Verbesserung einiger Qualitätsanforderungen, bei- spielsweise der Schaumqualität, erreicht werden kann, dies aber mit einer Verschlechterung anderer Qualitätsanforderungen, beispielsweise der haarpflegenden Eigenschaften, erkauft wird. Es bestand daher die Aufgabe, die Schaumqualität von Aerosolschäumen zur Haarbehand- lung zu verbessern, wobei gleichzeitig die haarpflegenden Eigenschaften nicht beeinträchtigt werden sondern idealerweise sogar ebenfalls verbessert werden.Aerosol foams for hair treatment are known and generally consist of hair-setting or hair-care substances, foaming agents and propellant gases and a suitable water-based solvent base. Various demands are placed on the quality of such aerosol foams, which can be roughly divided into two groups. One group of quality requirements relates to the quality of the foam, ie the nature of the foam. These include, for example, the fine or coarse pores, the compactness, the temporal stability of the foam, the incorporability and distributability on the hair, etc. The second group of quality requirements relates to the effects that the foam has on the hair after incorporation into the hair , ie the hair care properties such as, for example, the handle of the hair when wet and dry, the combability, the strengthening, the stress on the hair, etc. The problem with the optimization of aerosol foams is that although the addition of special active ingredients can improve some quality requirements, for example the foam quality, this is bought with a deterioration in other quality requirements, for example the hair-care properties. The object was therefore to improve the foam quality of aerosol foams for hair treatment, the hair care properties not being impaired at the same time, but ideally also being improved.
Es wurde nun gefunden, dass die Einarbeitbarkeit einer gut schäumenden und gut haarpflegenden Basis in das Haar erleichtert wird, wenn der Basis Entschäumer zugesetzt werden, welche ein schnelles Zusammenbrechen des Schaumes auf dem Haar fördern. Gleichzeitig werden die haarpflegenden Eigenschaften der Basis nicht verschlech- tert, sondern insbesondere bei Verwendung von Entschäumern auf Basis von Polydimethylsiloxan/Silica sogar noch weiter verbessert.It has now been found that the incorporation of a good lathering and hair-care base into the hair is facilitated if defoamers are added to the base, which promote rapid breakdown of the foam on the hair. At the same time, the hair care properties of the base are not deteriorated, but are even further improved, especially when using defoamers based on polydimethylsiloxane / silica.
Gegenstand der -Erfindung ist daher ein Aerosolschaum zur Haarbehandlung mit einem Gehalt anThe subject of the invention is therefore an aerosol foam for hair treatment containing
(A) mindestens einem kationischen, amphoteren oder zwitterionischen Polymer,(A) at least one cationic, amphoteric or zwitterionic polymer,
(B) mindestens einem Tensid,(B) at least one surfactant,
(C) mindestens einem Entschäumer, (D) einem wässrigen oder einem wässrig-alkoholischen Lösungsmittelsystem und (E) mindestens einem Aerosol-Treibmittel . Polymer (A )(C) at least one defoamer, (D) an aqueous or an aqueous-alcoholic solvent system and (E) at least one aerosol propellant. Polymer (A)
Das Polymer (A) ist in dem erfindungsgemäßen Mittel vorzugsweise in einer Menge von 0,01 bis 20, besonders bevorzugt von 0,02 bis 10, ganz besonders bevorzugt von 0,1 bis 5 Gewichtsprozent enthalten.The polymer (A) is contained in the agent according to the invention preferably in an amount of 0.01 to 20, particularly preferably from 0.02 to 10, very particularly preferably from 0.1 to 5 percent by weight.
Geeignete Polymere (A) sind solche, die auf Grund von kationischen oder kationisierbaren Gruppen, insbesondere primären, sekundären, tertiären oder vorzugsweise quaternären Amingruppen eine Substantivität zu menschlichem Haar aufweisen. Geeignete Polymere (A) sind ausgewählt aus Polymeren mit kationischen oder kationisierbaren Gruppen, polymeren Silikonverbindungen mit kationischen oder kationisierbaren Gruppen und kationisch derivatisierten Proteinen oder Protein- hydrolysaten. Bei den geeigneten kationaktiven Polymeren handelt es sich um haarfestigende und/oder um haar- konditionierende Polymere. Geeignete Polymere der Komponente (A) enthalten vorzugsweise quaternäre Amingruppen. Die kationischen Polymere können Homo- oder Copolymere sein, wobei die quaternären Stickstoffgruppen entweder in der Polymerkette oder vorzugsweise als Substituent- an einem oder mehreren der Monomeren enthalten sind. Die Ammoniumgruppen enthaltenden Monomere können mit nicht kationischen Monomeren copolymerisiert sein. Geeignete kationische Monomere sind ungesättigte, radikalisch polymerisierbare Verbindungen, welche mindestens eine kationische Gruppe tragen, insbesondere ammonium-substituierte Vinylmono- mere wie zum Beispiel Trialkylmethacryloxyalkylammo- nium, Trialkylacryloxyalkylammonium, Dialkyldiallyl- ammonium und quaternäre Vinylammoniummonomere mit cyclischen, kationische Stickstoffe enthaltenden Gruppen wie Pyridinium, Imidazolium oder quaternäre Pyrrolidone, z.B. Alkylvinylimidazolium, Alkylvinyl- pyridinium, oder Alyklvinylpyrrolidon Salze. Die Alkylgruppen dieser Monomere sind vorzugsweise niedere Alkylgruppen wie zum Beispiel Cl- bis C7-Alkylgruppen, besonders bevorzugt Cl- bis C3 -Alkylgruppen .Suitable polymers (A) are those which, owing to cationic or cationizable groups, in particular primary, secondary, tertiary or preferably quaternary amine groups, have a substantivity to human hair. Suitable polymers (A) are selected from polymers with cationic or cationizable groups, polymeric silicone compounds with cationic or cationizable groups and cationically derivatized proteins or protein hydrolyzates. The suitable cationic polymers are hair-setting and / or hair-conditioning polymers. Suitable polymers of component (A) preferably contain quaternary amine groups. The cationic polymers can be homo- or copolymers, the quaternary nitrogen groups being contained either in the polymer chain or preferably as a substituent on one or more of the monomers. The monomers containing ammonium groups can be copolymerized with non-cationic monomers. Suitable cationic monomers are unsaturated, free-radically polymerizable compounds which carry at least one cationic group, in particular ammonium-substituted vinyl monomers such as, for example, trialkylmethacryloxyalkylammonium, trialkylacryloxyalkylammonium, dialkyldiallylammonium and quaternary vinylammonium monomers containing cyclic, cationic nitrogenous substances Groups such as pyridinium, imidazolium or quaternary pyrrolidones, for example alkylvinylimidazolium, alkylvinylpyridinium, or alylvinylpyrrolidone salts. The alkyl groups of these monomers are preferably lower alkyl groups such as, for example, Cl to C7 alkyl groups, particularly preferably Cl to C3 alkyl groups.
Die Ammoniumgruppen enthaltenden Monomere können mit nicht-kationischen Monomeren copolymerisiert sein. Geeignete nicht-kationische Comonomere sind beispielsweise Acrylamid, Methacrylamid, Alkyl- und Dialkyl- acrylamid, Alkyl- und Dialkylmethacrylamid, Alkylacry- lat, Alkylmethacrylat , Vinylcaprolacton, Vinylcaprolac- tam, Vinylpyrrolidon, Vinylester, z.B. Vinylacetat, Vinylalkohol, Propylenglykol oder Ethylenglykol, wobei die Alkylgruppen dieser Monomere vorzugsweise Cl- bis C7-Alkylgruppen, besonders bevorzugt Cl- bis C3-Alkyl- gruppen sind.The monomers containing ammonium groups can be copolymerized with non-cationic monomers. Suitable non-cationic comonomers are, for example, acrylamide, methacrylamide, alkyl and dialkyl acrylamide, alkyl and dialkyl methacrylamide, alkyl acrylate, alkyl methacrylate, vinyl caprolactone, vinyl caprolactam, vinyl pyrrolidone, vinyl ester, e.g. Vinyl acetate, vinyl alcohol, propylene glycol or ethylene glycol, the alkyl groups of these monomers preferably being Cl to C7 alkyl groups, particularly preferably Cl to C3 alkyl groups.
Geeignete Polymere mit quaternären Amingruppen sind beispielsweise die im CTFA Cosmetic Ingredient Dictionary unter den Bezeichnungen Polyquaternium beschriebenen Polymere wie Dimethyldiallylammonium- chlorid/Acrylsäure Copolymer (Polyquaternium-22) , Methylvinylimidazoliumchlorid/Vinylpyrrolidon Copolymer (Polyquaternium-16) oder qüaternisiertes Vinylpyrroli- don/Dimethylaminoethylmethacrylat Copolymer (Polyquaternium-11) sowie quaternäre Silikonpolymere bzw. -oligomere wie beispielsweise Silikonpolymere mit quaternären Endgruppen (Quaternium-80) .Suitable polymers with quaternary amine groups are, for example, the polymers described in the CTFA Cosmetic Ingredient Dictionary under the names Polyquaternium, such as dimethyldiallylammonium chloride / acrylic acid copolymer (Polyquaternium-22), methylvinylimidazolium chloride / vinylpyrrolidone copolymer (Polyquaternium-16) or quaternized vinylpyramethyl-acrylate / vinylpyramethyl-copolymerized Polyquaternium-11) and quaternary silicone polymers or oligomers such as silicone polymers with quaternary end groups (Quaternium-80).
Von den kationischen Polymeren, die in dem erfindungs- gemäßen Mittel enthalten sein können, ist zum Beispiel Vinylpyrrolidon/Dimethylaminoethylmethacrylat Metho- sulfat Copolymer, das unter den Handelsbezeichnungen Gafquat® 755 N und Gafquat® 734 von der Firma Gaf Co., USA vertrieben wird und von denen das Gafquat® 734 besonders bevorzugt ist, geeignet. Weitere kationische Polymere sind beispielsweise das von der Firma BASF,Of the cationic polymers that can be contained in the agent according to the invention, for example vinylpyrrolidone / dimethylaminoethyl methacrylate is metho- sulfate copolymer available under the trade names Gafquat ® 755 N and Gafquat ® 734 Co., USA is sold by Gaf and of which the Gafquat ® 734 is particularly preferred suitable. Other cationic polymers include those from BASF,
Deutschland unter dem Handelsnamen LUVIQUAT® HM 550 vertriebene Copolymer aus Polyvinylpyrrolidon und Imidazoliminmethochlorid, das von der Firma Calgon/USA unter dem Handelsnamen Merquat" 280 vertriebene Copoly- mer aus Dimethyldiallylammoniumchlorid und Acrylsäure oder das Terpolymer Merquat Plus 3300 aus Dimethyldiallylammoniumchlorid, Natriumacrylat und Acrylamid, das von der Firma ISP/USA unter dem HandelsnamenGermany's copolymer of polyvinylpyrrolidone and imidazolimine methochloride sold under the trade name LUVIQUAT ® HM 550, the copolymer of dimethyldiallylammonium chloride and acrylic acid sold by the company Calgon / USA under the trade name Merquat "280 or the terpolymer Merquat Plus 3300 made of dimethyldiallylammonium chloride, sodium acrylate from the company ISP / USA under the trade name
Gaffix VC 713 vertriebene Terpolymer aus Vinyl- pyrrolidon, Dimethylaminoethylmethacrylat und Vinyl- caprolactam und das von der Firma Gaf unter demGaffix VC 713 sold terpolymer of vinyl pyrrolidone, dimethylaminoethyl methacrylate and vinyl caprolactam and that from Gaf under the
Handelsnamen Gafquat " HS 100 vertriebene Vinylpyrro- lidon/MethacrylamidopropyltrimethylammoniumchloridTrade names Gafquat "HS 100 vinylpyrrolidone / methacrylamidopropyltrimethylammonium chloride sold
Copolymer.Copolymer.
Geeignete kationische Polymere, die von natürlichen Polymeren abgeleitet sind, sind kationische Derivate von Polysacchariden, beispielsweise kationische Derivate von Cellulose, Stärke oder Guar. Geeignet sind^ weiterhin Chitosan und Chitosanderivate . Kationische Polysaccharide haben die allgemeine Formel (I)Suitable cationic polymers derived from natural polymers are cationic derivatives of polysaccharides, for example cationic derivatives of cellulose, starch or guar. Chitosan and chitosan derivatives are also suitable. Cationic polysaccharides have the general formula (I)
G-0-B-N+RaRbR° X" (I)G-0-BN + R a R b R ° X " (I)
G ist ein Anhydroglucoserest, beispielsweise Stärkeoder Celluloseanhydroglucose; B ist eine divalente Verbindungsgruppe, beispielsweise Alkylen, Oxyalkylen, Polyoxyalkylen oder Hydroxyalkylen;G is an anhydroglucose residue, e.g. starch or cellulose anhydroglucose; B is a divalent Linking group, for example alkylene, oxyalkylene, polyoxyalkylene or hydroxyalkylene;
Ra, Rb und Rc sind unabhängig voneinander Alkyl, Aryl, Alkylaryl, Arylalkyl, Alkoxyalkyl oder Alkoxyaryl mit jeweils bis zu 18 C-Atomen, wobei die Gesamtzahl der C- Atome in Ra, Rb und Rc vorzugsweise maximal 20 ist; X ist ein übliches Gegenanion, beispielsweise ein Halogen, Acetat, Phosphat, Nitrat oder Alkylsulfat, vorzugsweise ein Chlorid.R a , R b and R c are independently of one another alkyl, aryl, alkylaryl, arylalkyl, alkoxyalkyl or alkoxyaryl each having up to 18 C atoms, the total number of C atoms in R a , R b and R c preferably being a maximum of 20 is; X is a common counter anion, for example a halogen, acetate, phosphate, nitrate or alkyl sulfate, preferably a chloride.
Eine kationische Cellulose wird unter der Bezeichnung Polymer JR von Amerchol vertrieben und hat die INCI- Bezeichnung Polyquaternium-10. Eine weitere kationische Cellulose trägt die INCI -Bezeichnung Polyquaternium-24 und wird unter dem Handelsnamen Polymer LM-200 vonA cationic cellulose is sold under the name Polymer JR by Amerchol and has the INCI name Polyquaternium-10. Another cationic cellulose has the INCI name Polyquaternium-24 and is sold under the trade name Polymer LM-200 by
Amerchol vertrieben. Ein geeignetes kationisches Guar- derivat wird unter der Handelsbezeichnung Jaguar R vertrieben und hat die INCI-Bezeichnung Guar Hydroxy- propyltrimonium Chloride .Amerchol expelled. A suitable cationic guar derivative is sold under the trade name Jaguar R and has the INCI name guar hydroxypropyltrimonium chloride.
Besonders bevorzugte kationaktive Stoffe sind Chitosan, Chitosansalze und Chitosan-Derivate . Bei den erfindungsgemäß einzusetzenden Chitosanen handelt es sich um vollständig oder partiell deacetylierte Chitine. Zur Herstellung von Chitosan geht man vorzugsweise von dem in den Schalenresten von Krustentieren enthaltenem Chitin aus, welches als billiger und natürlicher Rohstoff in großen Mengen zur Verfügung steht. Das Molekulargewicht des Chitosans kann über ein breites Spektrum verteilt sein, beispielsweise von 20.000 bis ca. 5 Millionen g/mol . Geeignet ist beispielsweise ein niedermolekulares Chitosan mit einem Molekulargewicht von 30.000 bis 70.000 g/mol. Vorzugsweise liegt das Molekulargewicht jedoch über 100.000 g/mol, besonders bevorzugt von 200.000 bis 700.000 g/mol. Der Deacety- lierungsgrad beträgt vorzugsweise 10 bis 99%, besonders bevorzugt 60 bis 99%.Particularly preferred cationic substances are chitosan, chitosan salts and chitosan derivatives. The chitosans to be used according to the invention are completely or partially deacetylated chitins. The production of chitosan is preferably based on the chitin contained in the shell remains of crustaceans, which is available in large quantities as a cheap and natural raw material. The molecular weight of the chitosan can be distributed over a broad spectrum, for example from 20,000 to about 5 million g / mol. For example, a low molecular weight chitosan with a molecular weight of 30,000 to 70,000 g / mol is suitable. However, the molecular weight is preferably above 100,000 g / mol, particularly preferably from 200,000 to 700,000 g / mol. The degree of deacetylation is preferably 10 to 99%, particularly preferably 60 to 99%.
Ein geeignetes Chitosan wird beispielsweise von der Firma Kyowa Oil&Fat, Japan, unter dem HandelsnamenA suitable chitosan is, for example, from the company Kyowa Oil & Fat, Japan, under the trade name
Flonac vertrieben. Es hat ein Molekulargewicht von 300.000 bis 700.000 g/mol und ist zu 70 bis 80% ent- acetyliert. Ein bevorzugtes Chitosansalz ist Chitoso- niumpyrrolidoncarboxylat, welches beispielsweise unter der Bezeichnung Kytamer PC von der Firma Amerchol, USA, vertrieben wird. Das enthaltene Chitosan hat ein Molekulargewicht von ca. 200.000 bis 300.000 g/mol und ist zu 70 bis 85% entacetyliert . Als Chitosanderivate kommen quaternierte, alkylierte oder hydroxyalkylierte Derivate, beispielsweise Hydroxyethyl- , Hydroxypropyl- oder Hydroxybutylchitosan in Betracht .Flonac distributed. It has a molecular weight of 300,000 to 700,000 g / mol and is 70 to 80% deacetylated. A preferred chitosan salt is chitosonium pyrrolidone carboxylate, which is sold, for example, under the name Kytamer PC by Amerchol, USA. The chitosan contained has a molecular weight of approx. 200,000 to 300,000 g / mol and is 70 to 85% deacetylated. Quaternized, alkylated or hydroxyalkylated derivatives, for example hydroxyethyl, hydroxypropyl or hydroxybutyl chitosan, are suitable as chitosan derivatives.
Die Chitosane oder Chitosanderivate liegen vorzugsweise in neutralisierter oder partiell neutralisierter Form vor. Der Neutralisationsgrad für das Chitosan oder das Chitosanderivat liegt vorzugsweise bei mindestens 50%, besonders bevorzugt zwischen 70 und 100%, bezogen auf die Anzahl der "freien Basengruppen. Als Neutralisa- tionsmittel können prinzipiell alle kosmetisch verträglichen anorganischen oder organischen Säuren verwendet werden wie beispielsweise Ameisensäure, Weinsäure, Äpfelsäure, Milchsäure, Zitronensäure, Pyrrolidon- carbonsäure, Salzsäure u.a., von denen die Pyrrolidon- carbonsäure besonders bevorzugt ist.The chitosans or chitosan derivatives are preferably in neutralized or partially neutralized form. The degree of neutralization for the chitosan or the chitosan derivative is preferably at least 50%, particularly preferably between 70 and 100%, based on the number of "free base groups. Tion medium as Neutralisa- principle, all cosmetically compatible inorganic or organic acids can be used such as formic acid , Tartaric acid, malic acid, lactic acid, citric acid, pyrrolidone carboxylic acid, hydrochloric acid and others, of which pyrrolidone carboxylic acid is particularly preferred.
Bevorzugt sind solche Polymere, die eine ausreichende Löslichkeit in wässrigen oder wässrig-alkoholischen Lösungsmittelsystemen besitzen, um in dem erfindungsge- mäßen Mittel in vollständig gelöster Form vorzuliegen. Die kationische Ladungsdichte beträgt vorzugsweise 1 bis 7 meq/g.Preferred polymers are those which have sufficient solubility in aqueous or aqueous-alcoholic solvent systems in order to be able to medium in completely dissolved form. The cationic charge density is preferably 1 to 7 meq / g.
Geeignete kationaktive Silikonverbindungen weisen vorzugsweise entweder mindestens eine Aminogruppe oder mindestens eine Ammoniumgruppe auf. Geeignete Silikonpolymere mit Aminogruppen sind unter der INCI -Bezeichnung Amodimethicone bekannt. Hierbei handelt es sich um Polydimethylsiloxane mit Aminoalkylgruppen. Die Amino- alkylgruppen können Seiten- oder endständig sein. Geeignete Aminosilikone sind solche der allgemeinen Formel (II)Suitable cationic silicone compounds preferably have either at least one amino group or at least one ammonium group. Suitable silicone polymers with amino groups are known under the INCI name Amodimethicone. These are polydimethylsiloxanes with aminoalkyl groups. The aminoalkyl groups can be side or terminal. Suitable aminosilicones are those of the general formula (II)
R^ Si- (OSiR4R5)x- (OSiR6Q)y-OSiR7R8R9 (II)R ^ Si- (OSiR 4 R 5 ) x- (OSiR 6 Q) y-OSiR 7 R 8 R 9 (II)
R1, R2, R7 und R8 sind unabhängig voneinander gleich oder verschieden und bedeuten Cl- bis CIO -Alkyl, Phenyl, Hydroxy, Wasserstoff, Cl- bis ClO-Alkoxy oder Acetoxy, vorzugsweise C1-C4 -Alkyl, besonders bevorzugt Methyl ;R 1 , R 2 , R 7 and R 8 are independently the same or different and are Cl- to CIO-alkyl, phenyl, hydroxy, hydrogen, Cl- to ClO-alkoxy or acetoxy, preferably C1-C4-alkyl, particularly preferred Methyl;
R3 und R9 sind unabhängig voneinander gleich oder verschieden und bedeuten -(CH2)a-NH2 mit a gleich 1 bis 6, Cl- bis CIO -Alkyl, Phenyl, Hydroxy, Wasserstoff, Cl- bis ClO-Alkoxy oder Acetoxy, vorzugsweise C1-C4 -Alkyl, besonders bevorzugt Methyl ;R 3 and R 9 are independently the same or different and are - (CH 2 ) a -NH 2 with a equal to 1 to 6, Cl to CIO alkyl, phenyl, hydroxy, hydrogen, Cl to ClO alkoxy or acetoxy , preferably C1-C4-alkyl, particularly preferably methyl;
R4, R5 und R6 sind unabhängig voneinander gleich oder verschieden und bedeuten Wasserstoff, Cl- bis C20- Kohlenwasserstoff , welcher O- und N-Atome enthalten kann, vorzugsweise Cl- bis CIO-Alkyl oder Phenyl, besonders bevorzugt Cl- bis C4 -Alkyl, insbesondere Methyl;R 4 , R 5 and R 6 are independently the same or different and are hydrogen, Cl- to C20-hydrocarbon, which can contain O and N atoms, preferably Cl- to CIO-alkyl or phenyl, particularly preferably Cl- bis C4 alkyl, especially methyl;
Q bedeutet -A-NR^R11, oder -A-N+R10R1XR12 wobei A für eine divalente Cl- bis C20-Alkylenverbindungsgruppe steht, welche auch 0- und N-Atome sowie OH-Gruppen enthalten kann, und R10, R11 und R12 unabhängig voneinander gleich oder verschieden sind und Wasserstoff, Cl- bis C22- Kohlenwasserstoff , vorzugsweise Cl- bis C-4-Alkyl oder Phenyl bedeuten. Bevorzugte Reste für Q sindQ is -A-NR ^ R 11 , or -AN + R 10 R 1X R 12 where A is a divalent Cl to C20 alkylene linking group, which can also contain 0 and N atoms and OH groups, and R 10 , R 11 and R 12 are independently the same or different and are hydrogen, Cl to C22 hydrocarbon, preferably Cl to C-4 alkyl or Phenyl mean. Preferred radicals for Q are
- (CH2) 3-NH2 , - (CH2) 3NHCH2CH2NH2 , - (CH2) 3OCH2CHOHCH2NH2 und- (CH 2 ) 3 -NH 2 , - (CH 2 ) 3 NHCH 2 CH 2 NH 2 , - (CH 2 ) 3 OCH 2 CHOHCH 2 NH 2 and
- (CH2)3N(CH2CH2OH)2, -(CH2)3-NH3 + und- (CH 2 ) 3 N (CH 2 CH 2 OH) 2 , - (CH 2 ) 3 -NH 3 + and
- (CH2)3OCH2CHOHCH2N+(CH3)2R13, wobei R13 ein Cl- bis C22- Alkylrest ist, der auch OH-Gruppen aufweisen kann. X bedeutet eine Zahl zwischen 1 und 10.000, vorzugsweise zwischen 1 und 1.000;- (CH 2 ) 3 OCH 2 CHOHCH 2 N + (CH 3 ) 2 R 13 , where R 13 is a Cl to C22 alkyl radical, which may also have OH groups. X represents a number between 1 and 10,000, preferably between 1 and 1,000;
Y bedeutet eine Zahl zwischen 1 und 500, vorzugsweise zwischen 1 und 50.Y represents a number between 1 and 500, preferably between 1 and 50.
Das Molekulargewicht der Aminosilikone liegt vorzugsweise zwischen 500 und 100.000. Der Aminanteil (meq/g) liegt vorzugsweise im Bereich von 0,05 bis 2,3, besonders bevorzugt von 0,1 bis 0,5.The molecular weight of the aminosilicones is preferably between 500 and 100,000. The amine content (meq / g) is preferably in the range from 0.05 to 2.3, particularly preferably from 0.1 to 0.5.
Geeignete Silikonpolymere mit zwei endständigen quaternären Ammoniumgruppen sind unter der INCI-Bezeichnung Quaternium-80 bekannt. Hierbei handelt es sich um Di- methylsiloxane mit zwei endständigen Aminoalkylgruppen . Geeignete quaternäre Aminosilikone sind solche der allgemeinen Formel (III)Suitable silicone polymers with two terminal quaternary ammonium groups are known under the INCI name Quaternium-80. These are dimethylsiloxanes with two terminal aminoalkyl groups. Suitable quaternary aminosilicones are those of the general formula (III)
R1 R15R16N+ _A_ s iRlR2 _ ( os i R4R5 ) n_ os i RlR2 _A_N+R14R15R16 2 χ- ( J J J ) R 1 R 15 R 16 N + _ A _ s iR l R 2 _ (os i R 4 R 5 ) n _ os i R l R 2 _ A _ N + R 14 R 15 R 16 2 χ - (YYY)
A hat die gleiche Bedeutung wie oben bei Formel (II) angegeben und ist vorzugsweiseA has the same meaning as given above for formula (II) and is preferred
- (CH2)3OCH2CHOHCH2N+(CH3)2R13, wobei R13 ein Cl- bis C22- Alkylrest ist, der auch OH-Gruppen aufweisen kann; R1, R2, R4 und R5 haben die gleiche Bedeutung wie oben bei Formel (II) angegeben und sind vorzugsweise Methyl; R14, R15, und R16 bedeuten unabhängig voneinander Cl-bis C22-Alkylreste, welche Hydroxygruppen enthalten können und wobei vorzugsweise mindestens einer der Reste mindestens 10 C-Atome aufweist und die übrigen Reste 1 bis 4 C-Atome aufweisen; n ist eine Zahl von 0 bis 200, vorzugsweise 10 bis 100.- (CH 2 ) 3 OCH 2 CHOHCH 2 N + (CH 3 ) 2 R 13 , where R 13 is a Cl to C22 alkyl radical, which may also have OH groups; R 1 , R 2 , R 4 and R 5 have the same meaning as given above for formula (II) and are preferably methyl; R 14 , R 15 and R 16 independently of one another are C 1 to C 22 alkyl radicals which may contain hydroxyl groups and where preferably at least one of the radicals has at least 10 C atoms and the remaining radicals have 1 to 4 C atoms; n is a number from 0 to 200, preferably 10 to 100.
Derartige diquaternäre Polydimethylsiloxane werden von der Firma GOLDSCHMIDT/Deutschland unter den Handels- namen Abil® Quat 3270, 3272 und 3274 vertrieben.Such diquaternary polydimethylsiloxanes are sold by GOLDSCHMIDT / Germany under the trade names Abil ® Quat 3270, 3272 and 3274.
Weitere geeignete kationaktive, haarpflegende Verbindungen sind kationisch modifizierte Proteinderivate oder kationisch modifizierte Proteinhydrolysate und sind beispielsweise bekannt unter den INCI-Bezeich- nungen Lauryldimonium Hydroxypropyl Hydrolyzed Wheat Protein, Lauryldimonium Hydroxypropyl Hydrolyzed Casein, Lauryldimonium Hydroxypropyl Hydrolyzed Collagen, Lauryldimonium Hydroxypropyl Hydrolyzed Keratin, Lauryldimonium Hydroxypropyl Hydrolyzed Silk, Lauryldimonium Hydroxypropyl Hydrolyzed Soy Protein oder Hydroxypropyltrimonium Hydrolyzed Wheat, Hydroxypropyltrimonium Hydrolyzed Casein, Hydroxypropyltrimonium Hydrolyz"ed Collagen, Hydroxypropyltrimonium Hydrolyzed Keratin, Hydroxypropyltrimonium Hydrolyzed Rice Bran Protein, Hydroxypropyltrimonium Hydrolyzed Silk, Hydroxypropyltrimonium Hydrolyzed Soy Protein, Hydroxypropyltrimonium Hydrolyzed Vegetable Protein.Further suitable cationic, hair-care compounds are cationically modified protein derivatives or cationically modified protein hydrolyzates and are known, for example, under the INCI names lauryldimonium hydroxypropyl hydrolyzed wheat protein, lauryldimonium hydroxypropyl hydrolyzed casein, lauryldimonium hydroxypropyl hydrolyzed collagen, lauryldimonium hydroxypropyl, and lauryldimonium hydroxypropyl , Lauryidimonium hydroxypropyl or hydroxypropyltrimonium Hydrolyzed Soy protein Hydrolyzed Wheat, hydroxypropyltrimonium Hydrolyzed casein, hydroxypropyltrimonium Hydrolyz "ed collagen, hydroxypropyltrimonium Hydrolyzed keratin, hydroxypropyltrimonium Hydrolyzed Rice Bran protein, hydroxypropyltrimonium Hydrolyzed Silk, hydroxypropyltrimonium Hydrolyzed Soy protein, Hydrolyzed Vegetable protein hydroxypropyltrimonium.
Geeignete kationisch derivatisierte Proteinhydrolysate sind Substanzmischungen, die beispielsweise durch Umsetzung von alkalisch, sauer oder enzymatisch hydro- lysierten Proteinen mit Glycidyltrialkylammoniumsalzen oder 3-Halo-2-hydroxypropyltrialkylammoniumsalzen erhalten werden können. Proteine, die als Ausgangs- Stoffe für die Proteinhydrolysate dienen, können sowohl pflanzlicher als auch tierischer Herkunft sein. Übliche Ausgangsstoffe sind beispielsweise Keratin, Collagen, Elastin, Sojaprotein, Reisprotein, Milchprotein,Suitable cationically derivatized protein hydrolyzates are mixtures of substances which are obtained, for example, by reacting alkaline, acidic or enzymatically hydrolyzed proteins with glycidyltrialkylammonium salts or 3-halo-2-hydroxypropyltrialkylammonium salts can be obtained. Proteins that serve as starting materials for the protein hydrolyzates can be of both vegetable and animal origin. Common starting materials are, for example, keratin, collagen, elastin, soy protein, rice protein, milk protein,
Weizenprotein, Seidenprotein oder Mandelprotein. Durch die Hydrolyse entstehen Stoffmischungen mit Molmassen im Bereich von ca. 100 bis ca. 50.000. Übliche mittlere Molmassen liegen im Bereich von etwa 500 bis etwa 1000. Vorteilhafterweise enthalten die kationisch derivati- sierten Proteinhydrolysate eine oder zwei lange C8- bis C22-Alkylketten und entsprechend zwei oder eine kurze Cl- bis C4-Alkylketten. Verbindungen, die eine lange Alkylkette enthalten, sind bevorzugt.Wheat protein, silk protein or almond protein. The hydrolysis produces mixtures of substances with molecular weights in the range from approximately 100 to approximately 50,000. Usual average molecular weights are in the range from about 500 to about 1000. The cationically derivatized protein hydrolyzates advantageously contain one or two long C8 to C22 alkyl chains and correspondingly two or a short Cl to C4 alkyl chain. Compounds containing a long alkyl chain are preferred.
Geeignete amphotere Polymere sind solche, welche neben kationischen oder kationisierbaren basischen Gruppen, insbesondere primären, sekundären, tertiären oder quaternären Amingruppen, als weitere funktioneile Gruppen anionische oder anionisierbare saure Gruppen enthalten. Beispiele hierfür sind Copolymere gebildet aus Alkylacrylamid (insbesondere Octylacrylamid) , Alkylaminoalkylmethacrylat (insbesondere t-Butylamino- ethylmethacryla-t) und zwei oder mehr Monomeren beste- hend aus Acrylsäure, Methacrylsäure oder deren Ester (INCI -Bezeichnung: Octylacrylamide/Acrylates/Butyl- aminoethyl Methacrylate Copolymer) , wie sie zumSuitable amphoteric polymers are those which, in addition to cationic or cationizable basic groups, in particular primary, secondary, tertiary or quaternary amine groups, contain anionic or anionizable acidic groups as further functional groups. Examples of these are copolymers formed from alkyl acrylamide (in particular octylacrylamide), alkylaminoalkyl methacrylate (in particular t-butylaminoethyl methacrylate) and two or more monomers consisting of acrylic acid, methacrylic acid or their esters (INCI name: octylacrylamides / acrylates / butylaminoethyl) Methacrylate copolymer), such as
Beispiel unter dem Handelsnamen Amphomer oderExample under the trade name Amphomer or
Amphomer® LV-71 der Firma NATIONAL STARCH, USA erhält- lieh sind. Weitere geeignete amphotere Polymere sind Copolymere, welche gebildet sind aus mindestens einer ersten Monomerart, welche quaternäre Amingruppen aufweist und mindestens einer zweiten Monomerart, welche Säuregruppen aufweist. Beispiele für derartige Copoly- mere sind Copolymere von Acrylsäure, Methylacrylat und Methacrylamidopropyltrimethylammoniumchlorid ( INCI- Bezeichnung: Polyquaternium-47) , wie sie beispielsweise von der Firma Calgon unter der Handelsbezeichnung Merquat" 2001 vertrieben werden, Copolymere aus Acryl- amidopropyltrimethylammoniumchlorid und Acrylaten, wie sie beispielsweise von der Firma Stockhausen unter der Handelsbezeichnung W 37194 erhältlich sind oder Copolymere aus Acrylamid, Acrylamidopropyltrimethylammonium- chlorid, 2-Amidopropylacrylamidsulfonat und Dirnethyl- aminopropylamin (INCI-Bezeichnung: Polyquaternium-43) , wie sie beispielsweise von der Firma Societe FrancaiseAmphomer ® LV-71 from NATIONAL STARCH, USA. Further suitable amphoteric polymers are copolymers which are formed from at least one first type of monomer which has quaternary amine groups and at least one second type of monomer which has acid groups. Examples of such copoly mers are copolymers of acrylic acid, methyl acrylate and methacrylamidopropyltrimethylammonium chloride (INCI name: Polyquaternium-47), as are marketed, for example, by the company Calgon under the trade name Merquat "2001, copolymers of acrylamidopropyltrimethylammonium chloride and acrylates, as are used, for example, by the Stockhausen company are available under the trade name W 37194 or copolymers of acrylamide, acrylamidopropyltrimethylammonium chloride, 2-amidopropylacrylamide sulfonate and dirnethylaminopropylamine (INCI name: Polyquaternium-43), such as those from Societe Francaise
Hoechst unter der Handelsbezeichnung Bozequat 4000 vertrieben werden. Geeignet sind auch Polymere mit Betaingruppen tragenden Monomeren wie z.B. Copolymere aus Methacryloylethylbetain und zwei oder mehr Monomeren von Acrylsäure oder deren einfachen Estern, bekannt unter der INCI-Bezeichnung Methacryloyl Ethyl Betaine/ Acrylates Copolymer.Hoechst are sold under the trade name Bozequat 4000. Polymers with monomers bearing betaine groups, such as e.g. Copolymers of methacryloylethylbetaine and two or more monomers of acrylic acid or their simple esters, known under the INCI name Methacryloyl Ethyl Betaine / Acrylates Copolymer.
Tensid (V,)Surfactant (V,)
Das Tensid (B) ist in dem erfindungsgemäßen Mittel vorzugsweise in einer Menge von 0,01 bis 15, besonders bevorzugt von 0,05 bis 10 Gewichtsprozent enthalten. Geeignete Tenside haben emulgierende, lösungsvermittelnde, schaumbildende oder schaumverstärkende Eigenschaften und sind vorzugsweise nichtionisch. Generell läßt sich sagen, dass nicht-ionische Tenside für das erfindungsgemäße Haarbehandlungsmittel geeignet sind, wenn sie einen HLB-Wert von maximal 20, vorzugsweise von 5 bis 18 aufweisen. Bevorzugt sind dabei ethoxylierte Tenside, wobei die Anzahl der Ethylenoxid-Einheiten zwischen 1 bis 1000, bevorzugt zwischen 1 bis 300, besonders bevorzugt zwischen 1 und 15 liegt. Bevorzugt werden Fettsäure- glyceridethoxylate, Fettalkoholethoxylate, Fettamin- ethoxylate, Fettsäurealkanolamidethoxylate und Fett- säureesterethoxylate mit jeweils 1 bis 50 Ethylenoxid- einheiten. Beispiele für geeignete Fettalkoholethoxylate sind oxethylierter Lauryl-, Tetradecyl-, Cetyl-, Oleyl- oder Stearylalkohol, die allein oder im Gemisch eingesetzt werden können, sowie Fettalkohole von oxethy- liertem Lanolin oder oxethyliertes Lanolin. Auch die ethoxylierten Fettalkohole, die unter der Typenbezeich- nung Dehydol von der Firma Henkel oder unter der Typen- bezeichnung Brij® von der Firma ICI Surfactants vertrieben werden, sind für das erfindungsgemäße Haarbehandlungsmittel geeignet.The surfactant (B) is contained in the agent according to the invention preferably in an amount of 0.01 to 15, particularly preferably 0.05 to 10 percent by weight. Suitable surfactants have emulsifying, solubilizing, foam-forming or foam-enhancing properties and are preferably nonionic. In general, it can be said that non-ionic surfactants are suitable for the hair treatment composition according to the invention if they have an HLB value of at most 20, preferably from 5 to 18. Ethoxylated surfactants are preferred, the number of ethylene oxide units being between 1 and 1000, preferably between 1 and 300, particularly preferably between 1 and 15. Fatty acid glyceride ethoxylates, fatty alcohol ethoxylates, fatty amine ethoxylates, fatty acid alkanolamide ethoxylates and fatty acid ester ethoxylates each with 1 to 50 ethylene oxide units are preferred. Examples of suitable fatty alcohol ethoxylates are oxyethylated lauryl, tetradecyl, cetyl, oleyl or stearyl alcohol, which can be used alone or in a mixture, and fatty alcohols of oxyethylated lanolin or oxyethylated lanolin. The ethoxylated fatty alcohols, which are marketed under the type name Dehydol by Henkel or under the type name Brij ® by ICI Surfactants, are also suitable for the hair treatment composition according to the invention.
Unter den Fettsäureesterethoxylaten sind vor allem Diglyceridethoxylate zu nennen wie das von der ICIAmong the fatty acid ester ethoxylates, diglyceride ethoxylates such as that from ICI are particularly worth mentioning
Surfactants unter dem Handelnamen Arlatone G vertriebene, mit 25 Ethylenoxid-Einheiten ethoxylierte Rizinusöl mit dem INCI-Namen PEG-25 Hydrogenated Castor Oil, das von der BASF unter dem Handelnamen Cremophor El vertriebene, mit 35 Ethylenoxid-Einheiten ethoxylierte Rizinusöl mit dem INCI-Namen PEG-35 Castor Oil, das von der BASF unter dem Handelsnamen Cremophor® RH 410 vertriebene, mit 40 Ethylenoxid-Einheiten ethoxylierte, hydrierte Rizinusöl mit dem INCI-Namen PEG-40 Hydro- genated Castor Oil, und die von der Firma WitcoSurfactants sold under the trade name Arlatone G, castor oil with the INCI name PEG-25 Hydrogenated Castor Oil, ethoxylated with 25 ethylene oxide units, and castor oil with the INCI name sold by BASF under the trade name Cremophor El, with 35 ethylene oxide units PEG-35 Castor Oil, marketed by BASF under the trade name Cremophor ® RH 410, with 40 ethylene oxide units, ethoxylated hydrogenated castor oil with the INCI name PEG-40 hydro- genated Castor Oil, and from Witco
Surfactants unter dem Namen Rewoderm® LI vertriebenen Rohstoffe zu nennen. Bevorzugte nicht-ionische Tenside sind ethoxylierte Fettsäurezuckerester, insbesondere ethoxylierte Sorbitanfettsäureester, die als Polysorbate bekannt sind, aber auch nicht ethoxylierte Tenside, wie die Fettsäurezuckerester, die von der Firma ICI Surfactants unter dem Handelsnamen Tween und Arlacel® vertrieben werden sowie die Alkylpolyglycoside, die von der FirmaTo name surfactants sold under the name Rewoderm ® LI. Preferred nonionic surfactants are ethoxylated Fettsäurezuckerester, in particular ethoxylated sorbitan fatty acid esters known as polysorbates, but not ethoxylated surfactants, such as the Fettsäurezuckerester, sold by ICI Surfactants under the trade name Tween and Arlacel ®, as well as the alkyl polyglycosides, of the company
Henkel unter dem Handelsnamen Plantaren ® oder Planta- care oder von der Firma Seppic unter dem Handelsnamen Oramix vertrieben werden.Henkel under the trade name Plantaren ® or Plantacare or by the company Seppic under the trade name Oramix.
Entschäumer (C)Defoamer (C)
Der Entschäumer (C) ist in dem erfindungsgemäßen Aersol- haarschaum vorzugsweise in einer Menge von 0,001 bis 0,5, besonders bevorzugt von 0,005 bis 0,1 Gew.% enthalten. Bevorzugt werden nicht-organische Entschäumer, insbesondere solche auf Basis von physiologisch indifferenten Wirkkomponenten wie Polydimethylsiloxan/ Silica. Derartige Wirkstoffe sind bekannt unter derThe defoamer (C) is preferably present in the aerosol hair foam according to the invention in an amount of 0.001 to 0.5, particularly preferably 0.005 to 0.1% by weight. Non-organic defoamers are preferred, especially those based on physiologically indifferent active components such as polydimethylsiloxane / silica. Such active ingredients are known under the
Bezeichnung Simethicone. Hierbei handelt es sich um eine Mischung von Dimethiconen (Polydimethylsiloxanen) einer mittleren Kettenlänge von 200 bis 350 Dimethylsiloxan- einheiten und hydratisiertem Silica. Sie können einge- setzt werden in Form von Silicon-Antischaumemulsionen. Hierbei handelt es sich um wässrige Emulsionen von Simethiconen.Name Simethicone. This is a mixture of dimethicones (polydimethylsiloxanes) with an average chain length of 200 to 350 dimethylsiloxane units and hydrated silica. They can be used in the form of silicone antifoam emulsions. These are aqueous emulsions of simethicones.
Iiösungsmit.t.p.l.fiystem (D)Iiösungsmit.t.p.l.fiystem (D)
Das erfindungsgemäße Mittel wird in einem wässrigen oder in einem wässrig-alkoholischen Medium mit vorzugsweise mindestens 10 Gewichtsprozent Wasser konfektio- niert . Das Lösungsmittelsystem ist vorzugsweise in einer Menge von 50 bis 98, besonders bevorzugt von 75 bis 95 Gewichtsprozent enthalten. Als Alkohole können insbesondere die für kosmetische Zwecke üblicherweise verwendeten niederen Alkohole mit 1 bis 4 Kohlenstoff- atomen wie zum Beispiel Ethanol und Isopropanol enthalten sein. Das erfindungsgemäße Mittel kann in einem pH- Bereich von 2,0 bis 9,5 vorliegen. Besonders bevorzugt ist der pH-Bereich zwischen 3,5 und 8.The agent according to the invention is confectioned in an aqueous or in an aqueous-alcoholic medium with preferably at least 10 percent by weight of water. kidney. The solvent system is preferably contained in an amount of 50 to 98, particularly preferably 75 to 95 percent by weight. In particular, the lower alcohols with 1 to 4 carbon atoms usually used for cosmetic purposes, such as ethanol and isopropanol, can be included as alcohols. The agent according to the invention can be present in a pH range from 2.0 to 9.5. The pH range between 3.5 and 8 is particularly preferred.
Als zusätzliche Co-Solventien können organische Lösungsmittel oder ein Gemisch aus Lösungsmitteln mit einem Siedepunkt unter 400°C in einer Menge von 0,1 bis 15, bevorzugt von 1 bis 10 Gewichtsprozent enthalten sein. Besonders geeignet als zusätzliche Co-Solventien sind unverzweigte oder verzweigte Kohlenwasserstoffe wie Pentan, Hexan, Isopentan und cyclische Kohlenwasserstoffe wie Cyclopentan und Cyclohexan. Weitere, besonders bevorzugte wasserlösliche Lösungsmittel sind Glycerin, Ethylenglykol und Propylenglykol .Organic solvents or a mixture of solvents with a boiling point below 400 ° C. can be present as additional co-solvents in an amount of 0.1 to 15, preferably 1 to 10 percent by weight. Unbranched or branched hydrocarbons such as pentane, hexane, isopentane and cyclic hydrocarbons such as cyclopentane and cyclohexane are particularly suitable as additional co-solvents. Other particularly preferred water-soluble solvents are glycerol, ethylene glycol and propylene glycol.
Trei mittel [ElTrei medium [El
Das Treibmittel- (E) ist in dem erfindungsgemäßen Aersolhaarschaum vorzugsweise in einer Menge von 1 bis 20, besonders bevorzugt von- 2 bis 10 Gewichtsprozent enthalten. Als Treibmittel sind beispielsweise niedere Alkane, wie zum Beispiel n-Butan, i-Butan, Propan, Butan, oder auch deren Gemische sowie Dimethylether oder Fluorkohlenwasserstoffe wie F 152a (1, 1-Difluor- ethan) oder F 134 (Tetrafluorethan) sowie ferner bei den in Betracht kommenden Drücken gasförmig vorliegende Treibmittel, wie beispielsweise N2, N20 und C02 sowie Gemische der vorstehend genannten Treibmittel geeignet . In einer weiteren, bevorzugten Ausführungsform enthält das erfindungsgemäße Mittel zusätzlich 0,01 bis 15 Gewichtsprozent, vorzugsweise 0,5 bis 10 Gewichtspro- zent mindestens eines synthetischen oder natürlichen nichtionischen filmbildenden Polymers. Bevorzugt sind insbesondere solche Polymere, die eine ausreichende Löslichkeit in Wasser oder Wasser/Alkohol-Gemischen besitzen, um in dem erfindungsgemäßen Mittel in voll- ständig gelöster Form vorzuliegen. Unter filmbildenden Polymeren werden erfindungsgemäß solche Polymere verstanden, die bei Anwendung in 0,01 bis 5%-iger wässriger, alkoholischer oder wässrig-alkoholischer Lösung in der Lage sind, auf dem Haar einen Polymerfilm abzuscheiden.The blowing agent (E) is preferably present in the aerosol hair foam according to the invention in an amount of 1 to 20, particularly preferably 2 to 10 percent by weight. As blowing agents are, for example, lower alkanes, such as n-butane, i-butane, propane, butane, or also their mixtures, and also dimethyl ether or fluorocarbons such as F 152a (1,1-difluoroethane) or F 134 (tetrafluoroethane) and further suitable at the pressures under consideration gaseous blowing agents, such as N 2 , N 2 0 and C0 2, as well as mixtures of the blowing agents mentioned above. In a further preferred embodiment, the agent according to the invention additionally contains 0.01 to 15 percent by weight, preferably 0.5 to 10 percent by weight, of at least one synthetic or natural nonionic film-forming polymer. Particularly preferred are those polymers which have sufficient solubility in water or water / alcohol mixtures to be present in the agent according to the invention in completely dissolved form. According to the invention, film-forming polymers are understood to mean those polymers which, when used in 0.01 to 5% aqueous, alcoholic or aqueous-alcoholic solution, are able to deposit a polymer film on the hair.
Geeignete synthetische, nichtionische filmbildende, haarfestigende Polymere sind Homo- oder Copolymere, die aus mindestens einem der folgenden Monomere aufgebaut sind: Vinylpyrrolidon, Vinylcaprolactam, Vinylester wie z.B. Vinylacetat, Vinylalkohol, Acrylamid, Methacryl- amid, Alkyl- und Dialkylacrylamid, Alkyl- und Dialkyl- methacrylamid, Alkylacrylat , Alkylmethacrylat , Propy- lenglykol oder _Ethylenglykol , wobei die Alkylgruppen dieser Monomere vorzugsweise Cl- bis C7-Alkylgruppen, besonders bevorzugt Cl- bis C3 -Alkylgruppen sind.Suitable synthetic, nonionic film-forming, hair-fixing polymers are homopolymers or copolymers which are composed of at least one of the following monomers: vinylpyrrolidone, vinylcaprolactam, vinyl esters such as e.g. Vinyl acetate, vinyl alcohol, acrylamide, methacrylamide, alkyl and dialkylacrylamide, alkyl and dialkyl methacrylamide, alkyl acrylate, alkyl methacrylate, propylene glycol or ethylene glycol, the alkyl groups of these monomers preferably Cl to C7 alkyl groups, particularly preferably Cl to bis C3 are alkyl groups.
Geeignet sind z.B. Homopolymere des Vinylcaprolactams, des Vinylpyrrolidons oder des N-Vinylformamids . Weitere geeignete synthetische filmbildende, nicht-ionische, haarfestigende Polymere sind z.B. Copolymerisate aus Vinylpyrrolidon und Vinylacetat, Terpolymere aus Vinylpyrrolidon, Vinylacetat und Vinylpropionat , Polyacryl- amide, die beispielsweise unter den Handelsbezeichnungen Akypomine" P 191 von der Firma CHEM-Y, Emmerich, oder Sepigel® 305 von der Firma Seppic vertrieben werden; Polyvinylalkohole, die beispielsweise unter denHomopolymers of vinyl caprolactam, vinyl pyrrolidone or N-vinyl formamide are suitable, for example. Other suitable synthetic film-forming, non-ionic, hair-fixing polymers are, for example, copolymers of vinyl pyrrolidone and vinyl acetate, terpolymers of vinyl pyrrolidone, vinyl acetate and vinyl propionate, polyacrylamides, for example under the trade names Akypomine "P 191 sold by the company CHEM-Y, Emmerich or Sepigel ® 305 by the company SEPPIC; polyvinyl alcohols, for example, under the
Handelsbezeichnungen Elvanol von Du Pont oder Vinol® 523/540 von der Firma Air Products vertrieben werden sowie Polyethylenglykol/Polypropylenglykol-Copolymere, die beispielsweise unter den Handelsbezeichnungen Ucon® der Union Carbide vertrieben werden. Besonders bevorzugt sind Polyvinylpyrrolidon und Copolymere von Vinyl- pyrrolidon und nichtionischen Comoneren, beispielsweise Polyvinylpyrrolidon/Vinylacetat Copolymere .Trade names Elvanol from Du Pont or Vinol ® 523/540 from Air Products are sold, as well as polyethylene glycol / polypropylene glycol copolymers, which are sold, for example, under the trade names Ucon ® from Union Carbide. Polyvinylpyrrolidone and copolymers of vinylpyrrolidone and nonionic comoners, for example polyvinylpyrrolidone / vinyl acetate copolymers, are particularly preferred.
Geeignete natürliche filmbildende Polymere sind z.B. Cellulosederivate, z.B. Hydroxypropylcellulose mit einem Molekulargewicht von 30.000 bis 50.000 g/mol, welche beispielsweise unter der Handelsbezeichnung Nisso Sl ® von der Firma Lehmann & Voss, Hamburg, vertrieben wird.Suitable natural film-forming polymers are e.g. Cellulose derivatives, e.g. Hydroxypropyl cellulose with a molecular weight of 30,000 to 50,000 g / mol, which is sold, for example, under the trade name Nisso Sl ® by Lehmann & Voss, Hamburg.
Das erfindungsgemäße Mittel kann darüber hinaus die für Haarbehandlungsmittel üblichen Zusatzbestandteile enthalten, zum Beispiel Parfümöle in einer Menge von 0,01 bis 0,5 Gewichtsprozent; Trübungsmittel, wie zum Beispiel Ethylenglykoldistearat , in einer Menge von etwa 0,2 bis 5,0 Gewichtsprozent; Konservierungsmittel wie zum Beispiel Parabene in einer Menge von 0,01 bis 1,0 Gewichtsprozent; Puffersubstanzen, wie beispielsweise Natriumeitrat oder Natriumphosphat, in einer Menge von 0,1 bis 1,0 Gewichtsprozent; Pflegestoffe, wie zum Beispiel Pflanzen- und Kräuterextrakte, Protein- und Seidenhydrolysate, Lanolinderivate, in einer Menge von 0,1 bis 5 Gewichtsprozent; physiologisch verträgliche Silikonderivate, wie zum Beispiel flüchtige oder nicht- flüchtige Silikonöle oder hoch- molekulare Siloxanpolymere in einer Menge von 0,05 bis 20 Gew.%; Lichtschutzmittel, Antioxidantien, Radikalfänger, Antischuppenwirkstoffe, in einer Menge von etwa 0,01 bis 2 Gew.%; direktziehende Haarfarbstoffe, Haar- farbstoffe, die oxidativ entwickelt werden, Oxidations- mittel, Reduktionsmittel, Glanzgeber, Vitamine, Weichmacher, Kämmbarkeitsverbesserer und rückfettende Agenzien.The agent according to the invention can furthermore contain the additional ingredients customary for hair treatment agents, for example perfume oils in an amount of 0.01 to 0.5 percent by weight; Opacifiers, such as ethylene glycol distearate, in an amount of about 0.2 to 5.0 percent by weight; Preservatives such as parabens in an amount of 0.01 to 1.0 percent by weight; Buffer substances such as sodium citrate or sodium phosphate in an amount of 0.1 to 1.0 percent by weight; Care substances, such as plant and herbal extracts, protein and silk hydrolyzates, lanolin derivatives, in an amount of 0.1 to 5 percent by weight; physiologically compatible silicone derivatives, such as volatile or non-volatile silicone oils or highly molecular siloxane polymers in an amount of 0.05 to 20% by weight; Light stabilizers, antioxidants, radical scavengers, antidandruff agents, in an amount of about 0.01 to 2% by weight; direct hair dyes, hair dyes that are developed oxidatively, oxidizing agents, reducing agents, shine generators, vitamins, plasticizers, combability improvers and moisturizing agents.
Der erfindungsgemäße Aerosolschaum wird in einer druckfesten Aerosolverpackung abgefüllt, welche mit einem Aersolschaumkopf versehen wird. Beim Ausbringen aus dieser Aerosolverpackung bildet sich ein Schaum, welcher besonders leicht in das Haar eingearbeitet werden kann und der besonders schnell beim Einarbeiten auf dem Haar zusammenbricht .The aerosol foam according to the invention is filled in a pressure-resistant aerosol packaging which is provided with an aerosol foam head. When this aerosol packaging is applied, a foam forms which can be worked into the hair particularly easily and which breaks down particularly quickly when it is worked into the hair.
Das erfindungsgemäße kosmetische Mittel wird angewendet, indem es in einer zur Erzielung des gewünschten haarpflegenden oder haarfestigenden Effektes ausreichenden Menge auf feuchtes, handtuchtrockenes Haar aufgetragen und eingearbeitet wird und ohne Ausspülen im Haar belassen wird. Anschließend kann die Frisur in üblicher Weise -geformt werden bzw. können die Haare eingelegt und zum Schluß trocken gefönt werden. Es ist aber auch möglich, das Mittel direkt auf trockenem Haar' anzuwenden .The cosmetic agent according to the invention is applied by applying and incorporating it in an amount sufficient to achieve the desired hair-care or hair-fixing effect on damp, towel-dried hair and leaving it in the hair without rinsing. Then the hairstyle can be shaped in the usual way or the hair can be inserted and finally blow-dried. But it is also possible to use the product directly on dry hair.
Durch den Zusatz eines Entschäumers auf Basis von Poly- dimethylsiloxan/Silica (Simethicone) zu Aerosol-Haarschaumformulierungen kann ein auf dem Haar sehr schnell zusammenbrechender Schaum erhalten werden. Durch die sehr geringe Einsatzmenge (z.B. 0,01 - 0,5 Gew.%) werden die Pflege-Eigenschaften nicht beeinträchtigt sondern sogar verbessert, insbesondere der Griff feucht, die Kämmbarkeit, der Griff trocken und die Belastung des trockenen Haares.By adding a defoamer based on poly-dimethylsiloxane / silica (Simethicone) to aerosol hair foam formulations, a foam that breaks down very quickly on the hair can be obtained. The care properties are not impaired by the very small amount used (for example 0.01-0.5% by weight) but even improved, especially the wet grip, the combability, the dry grip and the strain on dry hair.
Die nachfolgenden Beispiele sollen den Gegenstand der Erfindung näher erläutern.The following examples are intended to explain the subject matter of the invention in more detail.
BeispieleExamples
Beispiel 1: Aerosol-Haarschaum:Example 1: Aerosol Hair Foam:
Die Wirkstoffmischung wurde im Verhältnis 92 : 8 mit Propan/n-Butan 4.8 bar als Treibmittel in einer Aerosoldose mit Schaumventil abgefüllt.The mixture of active ingredients was filled in a ratio of 92: 8 with propane / n-butane 4.8 bar as propellant in an aerosol can with a foam valve.
In Halbseitenversuchen wurde jeweils eine Hälfte der Haare von Testpersonen mit dem erfindungsgemäßen Aerosol-Schaum E und die andere Hälfte der Haare mit dem nicht erfindungsgemäßen Vergleichsschaum V behandelt. Die behandelten Haare wurden durch ausgebildete Friseurfachkräfte sensorisch beurteilt. Dabei wurden die folgenden Beurteilungen erhalten: Muster 1E weist gegenüber Muster IV eine verbesserte Schaumqualität auf, der Schaum bricht schneller zusammen und ist weniger stabil und kompakt.In half-side trials, half of the hair of test persons was treated with the aerosol foam E according to the invention and the other half of the hair with the comparison foam V not according to the invention. The treated hair was sensory assessed by trained hairdressers. The following assessments were obtained: Pattern 1E has an improved foam quality compared to pattern IV, the foam breaks down faster and is less stable and compact.
Die mit Muster 1E behandelten Haare haben einen besseren Griff des feuchten Haares als die mit Muster IV behandelten Haare. Die Haare fühlen sich leichter und weniger schmierig an.The hair treated with pattern 1E has a better grip on damp hair than the hair treated with pattern IV. The hair feels lighter and less greasy.
Die mit Muster 1E behandelten Haare weisen eine bessere Kämmbarkeit auf als die mit Muster IV behandelten Haare . Die mit Muster 1E behandelten Haare haben einen besseren Griff des trockenen Haares als die mit Muster IV behandelten Haare. Die Haare fühlen sich leichter und weniger ölig an.The hair treated with sample 1E has better combability than the hair treated with sample IV. The hair treated with pattern 1E has a better grip on dry hair than the hair treated with pattern IV. The hair feels lighter and less oily.
Die mit Muster 1E behandelten Haare weisen eine geringere Belastung auf als die mit Muster IV behandelten Haare .The hair treated with sample 1E has a lower load than the hair treated with sample IV.
Beispiel 2Example 2
Die Wirkstoffmischung wurde im Verhältnis 92:8 mit Propan/n-Butan 4.8 bar als Treibmittel in einer Aerosoldose mit Schaumventil abgefüllt. Beispiel 3The mixture of active ingredients was filled in a ratio of 92: 8 with propane / n-butane 4.8 bar as propellant in an aerosol can with a foam valve. Example 3
Die Wirkstoffmischung wurde im Verhältnis 94:6 mit Propan/n-Butan 4.8 bar als Treibmittel in einer Aerosoldose mit Schaumventil abgefüllt.The mixture of active ingredients was filled in a ratio of 94: 6 with propane / n-butane 4.8 bar as propellant in an aerosol can with a foam valve.
Beispiel 4Example 4
1( wässrige Lösung von PEG-200 Hydrogenated Glyceryl Palmate und PEG-7 Glyceryl Cocoat 1 ( aqueous solution of PEG-200 Hydrogenated Glyceryl Palmate and PEG-7 Glyceryl Cocoat
Die Wirkstoffmischung wurde im Verhältnis 92 : 8 mit Propan/n-Butan 4.8 bar als Treibmittel in einer Aerosoldose mit Schaumventil abgefüllt. The mixture of active ingredients was filled in a ratio of 92: 8 with propane / n-butane 4.8 bar as propellant in an aerosol can with a foam valve.
Claims
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
AU63833/01A AU6383301A (en) | 2000-04-18 | 2001-04-04 | Aerosol foam for treating hair |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE2000119128 DE10019128A1 (en) | 2000-04-18 | 2000-04-18 | Aerosol foam for hair treatment |
DE10019128.2 | 2000-04-18 |
Publications (2)
Publication Number | Publication Date |
---|---|
WO2001078661A2 true WO2001078661A2 (en) | 2001-10-25 |
WO2001078661A3 WO2001078661A3 (en) | 2002-03-14 |
Family
ID=7639136
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/EP2001/003799 WO2001078661A2 (en) | 2000-04-18 | 2001-04-04 | Aerosol foam for treating hair |
Country Status (4)
Country | Link |
---|---|
JP (1) | JP2001302468A (en) |
AU (1) | AU6383301A (en) |
DE (1) | DE10019128A1 (en) |
WO (1) | WO2001078661A2 (en) |
Cited By (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2834514A1 (en) * | 2002-01-10 | 2003-07-11 | Oreal | Aerosol device useful for hair styling includes a film-forming polymer dissolved or finely dispersed in a water-in-oil emulsion containing a silicone emulsifier |
EP1391192A1 (en) * | 2002-08-12 | 2004-02-25 | Beiersdorf Aktiengesellschaft | Cosmetic post-foaming preparations |
DE102004041294A1 (en) * | 2004-08-25 | 2006-03-09 | Beiersdorf Ag | Hair fixing agent also imparting care includes 2 or 3 cationic polymers of different weight average molecular weight ranges, a nonionic polymer and a surfactant |
WO2007001843A1 (en) * | 2005-06-20 | 2007-01-04 | The Procter & Gamble Company | A product release system to atomize compositions containing hair-conditioning ingredients |
WO2007002048A1 (en) * | 2005-06-20 | 2007-01-04 | The Procter & Gamble Company | A product release system for atomizing cosmetic hair compositions containing cationic polymers |
WO2007002045A1 (en) * | 2005-06-20 | 2007-01-04 | The Procter & Gamble Company | Product release system to atomize polymer-containing cosmetic hair compositions |
WO2006131401A3 (en) * | 2005-06-10 | 2007-03-15 | Galderma Sa | Controlled release of a drug through skin on the basis of a topical composition comprising a drug, a film-forming silicone and at least one volatile solvent |
US10603261B2 (en) | 2014-12-19 | 2020-03-31 | The Procter And Gamble Company | Composition for enhancing hair fiber properties |
US11129780B2 (en) | 2016-01-29 | 2021-09-28 | The Procter And Gamble Company | Composition for enhancing hair fiber properties |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE10321373A1 (en) * | 2003-05-13 | 2004-12-02 | Beiersdorf Ag | Sprayable polymer-containing preparation for hair styling when the spray hits a hairstyle surface and forms an unstable and rapidly disintegrating foam |
KR20090120014A (en) | 2003-12-12 | 2009-11-23 | 바이엘 크롭사이언스 아게 | Synergistic insecticidal mixture |
Family Cites Families (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE4343378C1 (en) * | 1993-12-18 | 1995-03-30 | Kao Corp Gmbh | Hair care composition |
US5599532A (en) * | 1994-08-12 | 1997-02-04 | Chesebrough-Pond's Usa Co., Division Of Conopco, Inc. | Sprayable hair treatment composition |
JPH10226627A (en) * | 1997-02-18 | 1998-08-25 | Kao Corp | Foam hair cosmetic |
DE19825961B4 (en) * | 1998-06-10 | 2006-04-27 | Kpss-Kao Professional Salon Services Gmbh | Aerosol foam composition for conditioning human hair |
GB9822419D0 (en) * | 1998-10-14 | 1998-12-09 | Unilever Plc | Hair styling composition |
-
2000
- 2000-04-18 DE DE2000119128 patent/DE10019128A1/en not_active Withdrawn
- 2000-04-21 JP JP2000121097A patent/JP2001302468A/en active Pending
-
2001
- 2001-04-04 AU AU63833/01A patent/AU6383301A/en not_active Abandoned
- 2001-04-04 WO PCT/EP2001/003799 patent/WO2001078661A2/en active Application Filing
Cited By (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2834514A1 (en) * | 2002-01-10 | 2003-07-11 | Oreal | Aerosol device useful for hair styling includes a film-forming polymer dissolved or finely dispersed in a water-in-oil emulsion containing a silicone emulsifier |
EP1391192A1 (en) * | 2002-08-12 | 2004-02-25 | Beiersdorf Aktiengesellschaft | Cosmetic post-foaming preparations |
DE102004041294A1 (en) * | 2004-08-25 | 2006-03-09 | Beiersdorf Ag | Hair fixing agent also imparting care includes 2 or 3 cationic polymers of different weight average molecular weight ranges, a nonionic polymer and a surfactant |
WO2006131401A3 (en) * | 2005-06-10 | 2007-03-15 | Galderma Sa | Controlled release of a drug through skin on the basis of a topical composition comprising a drug, a film-forming silicone and at least one volatile solvent |
AU2006256860B2 (en) * | 2005-06-10 | 2012-04-19 | Galderma S.A. | Controlled release of a drug through skin on the basis of a topical composition comprising a drug, a film-forming silicone and at least one volatile solvent |
WO2007001843A1 (en) * | 2005-06-20 | 2007-01-04 | The Procter & Gamble Company | A product release system to atomize compositions containing hair-conditioning ingredients |
WO2007002048A1 (en) * | 2005-06-20 | 2007-01-04 | The Procter & Gamble Company | A product release system for atomizing cosmetic hair compositions containing cationic polymers |
WO2007002045A1 (en) * | 2005-06-20 | 2007-01-04 | The Procter & Gamble Company | Product release system to atomize polymer-containing cosmetic hair compositions |
US10603261B2 (en) | 2014-12-19 | 2020-03-31 | The Procter And Gamble Company | Composition for enhancing hair fiber properties |
US11129780B2 (en) | 2016-01-29 | 2021-09-28 | The Procter And Gamble Company | Composition for enhancing hair fiber properties |
US11986542B2 (en) | 2016-01-29 | 2024-05-21 | The Procter & Gamble Company | Composition for enhancing hair fiber properties |
Also Published As
Publication number | Publication date |
---|---|
DE10019128A1 (en) | 2001-11-15 |
AU6383301A (en) | 2001-10-30 |
WO2001078661A3 (en) | 2002-03-14 |
JP2001302468A (en) | 2001-10-31 |
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