FR3130598A1 - Cosmetic or dermatological composition comprising a merocyanine and di-t-butyl pentaerythrityl tetra hydroxycinnamate - Google Patents

Abstract

Cosmetic or dermatological composition comprising a merocyanine and di-t-butyl pentaerythrityl tetra hydroxycinnamate The present invention relates to a composition, in particular a cosmetic or dermatological composition, comprising: a) at least one merocyanine corresponding to the following formula (3), as well as their isomeric geometric forms, including E/E or E/Z: [Formula 3] where: A is –O- or –NH; R is a C1-C22 alkyl group, a C2-C22 alkenyl group, a C2-C22 alkinyl group, a C3-C22 cycloalkyl group or a C3-C22 cycloalkenyl group, said groups possibly being interrupted by one or more O; and b) di-t-butyl pentaerythrityl tetra hydroxycinnamate. The present invention also relates to a non-therapeutic cosmetic process for caring for and/or making up a keratin material comprising the application to the surface of said keratin material of at least one composition as defined above.

Description

Cosmetic or dermatological composition comprising a merocyanine and di-t-butyl pentaerythrityl tetra hydroxycinnamate

The present invention relates to a cosmetic or dermatological composition comprising at least one merocyanine of formula (3) which will be defined in detail below and di-t-butyl pentaerythrityl tetra hydroxycinnamate.

The present invention also relates to a non-therapeutic cosmetic process for caring for and/or making up a keratin material comprising the application to the surface of said keratin material of at least one composition according to the invention as defined above. .

It also relates to a non-therapeutic cosmetic process for limiting the darkening of the skin and/or improving the color and/or the uniformity of the complexion comprising the application to the surface of the keratin material of at least one composition such as previously defined.

It also relates to a non-therapeutic cosmetic process for preventing and/or treating the signs of aging of a keratin material comprising the application to the surface of the keratin material of at least one composition as defined above.

It is known that radiation with a wavelength between 280 nm and 400 nm allows the human epidermis to be tanned and that radiation with a wavelength between 280 and 320 nm, known as UV-rays B are detrimental to the development of the natural tan. Exposure is also likely to induce an alteration of the biomechanical properties of the epidermis which results in the appearance of wrinkles leading to premature aging of the skin.

It is also known that UV-A rays with wavelengths between 320 and 400 nm penetrate deeper into the skin than UV-B rays. UV-A rays cause immediate and persistent darkening of the skin. Daily exposure to UVA rays, even of short duration, under normal conditions can lead to a breakdown of collagen fibers and elastin which results in a modification of the micro-relief of the skin, the appearance of wrinkles and a irregular pigmentation (brown spots, uneven skin tone).

Protection against UVA and UVB radiation is therefore necessary. An effective photo-protection product must protect against both UVA and UVB radiation.

Many photo-protective compositions have been proposed to date to remedy the effects induced by UVA and/or UVB radiation. They generally contain organic UV filters and/or inorganic UV filters which function according to their own chemical nature and according to their own properties by absorption, reflection, or diffusion of UV radiation. They generally contain mixtures of fat-soluble organic filters and/or water-soluble UV filters combined with metal oxide pigments such as titanium dioxide or zinc oxide.

Numerous cosmetic compositions intended to limit the darkening of the skin, to improve the color and the homogeneity of the complexion have been proposed to date. It is well known in the field of sunscreen products that such compositions can be obtained by using UV filters, and in particular UVB filters. Certain compositions may also contain UVA filters. This filtering system must cover UVB protection in order to limit and control the neo-synthesis of melanin favoring global pigmentation, but must also cover UVA protection in order to limit and control the oxidation of already existing melanin leading to darkening of skin color.

However, it is extremely difficult to find a composition containing a particular combination of UV filters which would be specially adapted to the photo-protection of the skin and particularly to an improvement in the quality of the skin both in terms of color and of its mechanical properties of elasticity.

Advantageously, this improvement is particularly sought after on skin that is already pigmented with the aim of not increasing either the pigmentary melanin load or the structure of the melanin already present within the skin.

In fact, the majority of organic UV filters consist of aromatic compounds that absorb in the wavelength range between 280 and 370 nm. In addition to their filtering power against solar radiation, the desired photo-protection compounds must also have good cosmetic properties, good solubility in the usual solvents and in particular in fatty substances such as oils or in water, as well as good photo-stability alone or in combination with other UV filters. They must also be colorless or at least present a cosmetically acceptable color for the consumer.

One of the main disadvantages known to date of these compositions is that these filtering systems have insufficient effectiveness against UV radiation and particularly against long UVA radiation with wavelengths beyond 370 nm in order to control pigmentation. photo-induced and its evolution by a UV filtering system on the entire UV spectrum.

Among all the compounds which have been recommended for this effect, an interesting family of UV filters has been proposed which consists of carbonaceous merocyanine derivatives which is described in patent US4195999, application WO2004/006878 and document IP COM Journal 4 ( 4), 16 No. IPCOM000011179D published on 04/03/2004. These compounds have very good filtration properties in long UVA rays but have a poorly satisfactory solubility in the usual solvents, both in the aqueous phase and in the fatty phase, and an unsatisfactory photostability for certain merocyanins.

With the aim of seeking other merocyanines having better solubility in the usual solvents and better photostability, application WO2013/011094 has proposed merocyanines comprising polar groups consisting of hydroxyl and ether functions which show a good long UVA filtration efficiency. However, the photostability of these particular merocyanins is not yet fully satisfactory, when used alone or in combination with other filters.

There therefore remains the need to improve the photostability of these merocyanins in photo-protective formulations, whether these are dissolved in the aqueous phase and/or in the fatty phase, while obtaining good cosmeticity.

The Applicant has discovered, surprisingly, that by using pentaerythrityl di-t-butyl tetrahydroxycinnamate, it is possible to significantly improve the photostability of these merocyanins both in an aqueous phase and in a fatty phase. This discovery is the basis of the present invention.

Thus, in accordance with one of the objects of the present invention, a cosmetic or dermatological composition is now proposed comprising at least one merocyanine of formula (3) which will be defined in detail below and tetra hydroxycinnamate di-t -butyl pentaerythrityl.

In addition, it also subsidizes the need to improve the photostability of merocyanins in the presence of organic filters such as, for example, dibenzoylmethane derivatives. Indeed, the addition of additional screening agents, in particular of dibenzoylmethane derivatives, can destabilize the compositions comprising a merocyanine.

Dibenzoylmethane derivatives, and in particular 4-ter-butyl-4'-methoxydibenzoyl methane, constitute a family of particularly effective UV-A screening agents which have a high intrinsic absorption power. These dibenzoylmethane derivatives, which are now products well known per se as active filters in UV-A, are described in particular in French patent applications FR-A-2326405 and FR-A-2440933, as well as in application European Patent EP-A-0114607; 4-ter-butyl-4′-methoxydibenzoyl methane is moreover currently offered for sale under the trade name “PARSOL 1789®” by the company DSM NUTRITIONAL PRODUCTS.

However, it has been observed that the combinations of merocyanine derivatives with dibenzoylmethane derivatives have the disadvantage of being particularly photo-unstable with regard to ultraviolet radiation (especially UV-A). These particular combinations of UV filters degrade more or less rapidly under the action of UV radiation; this degradation being particularly significant for the merocyanine derivatives. Thus, this substantial lack of photochemical stability of the combination of merocyanine derivatives with dibenzoylmethane derivatives against the ultraviolet radiation to which this combination is by nature intended to be subjected, does not make it possible to guarantee constant protection during prolonged exposure to the sun, so that repeated applications at regular and close time intervals must be carried out by the user to obtain effective and lasting protection of the skin against UV rays.

There is therefore also a real need to photostabilize the combination of merocyanine derivatives with dibenzoylmethane derivatives with respect to UV radiation, in order to guarantee constant protection during prolonged sun exposure with respect to UV-A radiation. .

The Applicant has surprisingly discovered that by using di-t-butyl pentaerythrityl tetra hydroxycinnamate, it is possible to significantly improve the photostability of these merocyanins in an aqueous phase or in a fatty phase even in the presence of organic UV filters. additional, in particular dibenzoylmethane derivatives.

The Applicant has also discovered that the use of di-t-butyl pentaerythrityl tetrahydroxycinnamate made it possible to obtain good cosmeticity of the composition comprising the merocyanins, the latter being in particular non-greasy and non-sticky.

The present invention also relates to a non-therapeutic cosmetic process for caring for and/or making up a keratin material comprising the application to the surface of said keratin material of at least one composition according to the invention as defined above. .

It also relates to a non-therapeutic cosmetic process for limiting the darkening of the skin and/or improving the color and/or the uniformity of the complexion comprising the application to the surface of the keratin material of at least one composition such as previously defined.

It also relates to a non-therapeutic cosmetic process for preventing and/or treating the signs of aging of a keratin material comprising the application to the surface of the keratin material of at least one composition as defined above.

The present invention also relates to the use of di-t-butyl pentaerythrityl tetra hydroxycinnamate for photostabilizing a merocyanine of formula (3) as defined below, alone or in the presence of an additional screening agent, in particular in the presence of a or more derivatives of dibenzoyl methane such as 4-ter-butyl-4'-methoxydibenzoyl methane.

Other characteristics, aspects and advantages of the invention will appear on reading the detailed description which follows.

The composition according to the invention is intended for topical application and therefore contains a physiologically acceptable medium. Here, the term “physiologically acceptable medium” means a medium compatible with keratin materials.

In the context of the present invention, the term “keratin material” is understood to mean in particular the skin, the scalp, the keratin fibers such as the eyelashes, the eyebrows, the hair, and the body hair, the nails, the mucous membranes such as the lips , and more particularly the skin and the mucous membranes (body, face, eye contour, eyelids, lips, preferably body, face and lips).

In what follows, and unless otherwise indicated, the limits of a domain of values are included in this domain, in particular in the expressions “included between” and “ranging from … to …”.

Furthermore, the expressions “at least one” and “at least” used in the present description are respectively equivalent to the expressions “one or more” and “greater than or equal”.

By "preventing" or "prevention" is meant according to the invention the fact of reducing the risk of occurrence or of slowing down the occurrence of a given phenomenon, namely, according to the present invention, the signs of aging of a material keratin.

By the expressions “optionally substituted” and “substituted or unsubstituted”, it is meant that the radical or group can be optionally substituted by one or more hydroxy; amino group -NR1R2, such that R1 and R2 represent, independently of one another, hydrogen atoms or C1-C3 alkyl radicals; carboxylic group –COOH, carbonyl, or C1-C4 alkyl.

MEROCYANINS

According to the present invention, a family of merocyanines corresponding to the following formula (3) as well as their isomeric geometric forms, in particular E/E- or E/Z-, will be used:
[Formula 3]
in which :
A is –O- or –NH;
R is a C ₁ -C ₂₂ alkyl group, a C ₂ -C ₂₂ alkenyl group, a C ₂ -C ₂₂ alkinyl group, a C ₃ -C ₂₂ cycloalkyl group or a C ₃ -C ₂₂ cycloalkenyl , said groups possibly being interrupted by one or more O.

The merocyanine compounds of the invention may be in their E/E-, E/Z- isomeric geometric forms:
[form 3]

The even more preferred compounds of formula (3) are those where:
A is -O-; R is a C ₁ -C ₂₂ alkyl, which can be interrupted by one or more O.

Among the compounds of formula (3), use will be made more particularly of those chosen from the following group as well as their isomeric geometric forms, in particular E/E-, E/Z-: 14
ethyl (2Z)-cyano{3-[(3-methoxypropyl)amino]cyclohex-2-en-1-ylidene}ethanoate 15
(2Z)-2-cyano-N-(3-methoxypropyl)-2-{3-[(3-methoxypropyl)amino]cyclohex-2-en-1-ylidene}ethanamide 25
2-ethoxyethyl (2Z)-cyano{3-[(3-methoxypropyl)amino]cyclohex-2-en-1-ylidene}ethanoate 27
2-methylpropyl (2Z)-cyano{3-[(3-methoxypropyl)amino]cyclohex-2-en-1-ylidene}ethanoate 29

2-butoxyethyl (2Z)-cyano{3-[(3-methoxypropyl)amino]cyclohex-2-en-1-ylidene}ethanoate 31

3-methoxypropyl (2Z)-cyano{3-[(3-methoxypropyl)amino]cyclohex-2-en-1-ylidene}ethanoate
37
3-ethoxypropyl (2Z)-cyano{3-[(3-methoxypropyl)amino]cyclohex-2-en-1-ylidene}ethanoate

According to a more particularly preferred embodiment of the invention, the compound 2-ethoxyethyl (2Z)-cyano{3-[(3-methoxypropyl)-amino]cyclohex-2-en-1-ylidene}ethanoate (25) will be used in its geometric configuration E/E and/or E/Z.

The E/Z shape has the following structure:
[form 25]

The E/E form has the following structure:
[form 25bis]

The screening merocyanins in accordance with the invention may be present in the compositions according to the invention in a concentration ranging from 0.1% to 15% by weight, and preferably from 0.2% to 10% by weight and even better from 0.5% to 5% by weight relative to the total weight of the composition.

The compounds of formula (3), which form a carbocyclic ring containing 6 carbon atoms, can be prepared according to the protocols described in Pat. Appl. WO 2007/071582, in IP.com Journal (2009), 9(5A), 29-30 IPCOM000182396D under the title “Process for producing 3-amino-2-cyclohexan-1-ylidene compounds” and in US-A-4,749,643 on col, 13, line 66 – col. 14, line 57 and references cited therein.

In particular, the compounds of formula (3), such as the compound 2-ethoxyethyl (2Z)-cyano{3-[(3-methoxypropyl)-amino]cyclohex-2-en-1-ylidene}ethanoate (25) can be synthesized according to the synthetic scheme described in the publication by B. Winkler et al., Tetrahedron Letters, 55 (2014) 1749-1751, which is entitled “A cyclic merocyanine UV-A absorber: mechanism of formation and crystal structure” , and represented below, for the compounds of formula (3):
[form 4]
And more particularly for compound 25 described in Table 1:
[form 5]
DI-T-BUTYL PENTAERYTHRITYL TETRA HYDROXYCINNAMATE

The composition in accordance with the invention comprises di-t-butyl pentaerythrityl tetra hydroxycinnamate.

Di-t-butyl pentaerythrityl tetra hydroxycinnamate or tetra-di-t-butyl hydroxyhydrocinnamate pentaerythrityl is a compound, which is part of the family of cinnamic acids and their derivatives, whose CAS number is 6683-19-8.

By way of example, mention may be made of the di-t-butyl pentaerythrityl tetrahydroxycinnamate compound marketed by the company BASF under the name Tinogard ^TT® .

Preferably, a composition according to the invention comprises from 0.01% to 2.5% by weight, preferably from 0.05% to 1.5% by weight, more preferably from 0.1% to 0.3% by weight of di-t-butyl pentaerythrityl tetrahydroxycinnamate compound, relative to the total weight of the composition.

COMPOUNDS DERIVED FROM DIBENZOYLMETHANE

According to a particular embodiment, the composition according to the present invention also comprises one or more dibenzoylmethane derivatives chosen from those of the following formula and/or mixtures thereof:
[form 6]

in which :
R1, R4, R5 and R6 represent, independently of each other, a hydrogen atom; a hydroxy radical; an alkyl radical, linear or branched, C1-C4; or an alkoxy radical, linear or branched, C1-C4; And
R2 and R3 represent, independently of each other, a hydrogen atom; a hydroxy radical; an alkyl radical, linear or branched, C1-C4; an alkoxy radical, linear or branched, C1-C4; or form with the 2 carbon atoms of the C-R2 and C-R3 covalent bonds a 5- or 6-membered heterocycle optionally substituted by a hydrocarbon chain, linear or branched, C1-C4.

When R2 and R3 form a heterocycle with the 2 carbon atoms of the covalent bonds C-R2 and C-R3, preferably they form a 5-membered aromatic heterocycle, more preferably a furan ring.

Preferably, R2 and R3 represent, independently of each other, a hydrogen atom; a hydroxy radical; an alkyl radical, linear or branched, C1-C4; an alkoxy radical, linear or branched, C1-C4.

According to a preferred embodiment of the invention, the compound(s) derived from dibenzoylmethane are chosen, alone or as a mixture, from 2-methyldibenzoylmethane, 4-methyldibenzoylmethane, 4-isopropyldibenzoylmethane, 4-tert-butyldibenzoylmethane, 2 ,4-dimethyldibenzoylmethane, 2,5-dimethyldibenzoylmethane, 4,4'-diisopropyldibenzoylmethane, 4,4'-dimethoxydibenzoylmethane, 4-tert-butyl-4'-methoxydibenzoylmethane, 2-methyl-5-isopropyl-4 '-methoxydibenzoylmethane, 2-methyl-5-tert-butyl-4'-methoxydi-benzoylmethane, 2,4-dimethyl-4'-methoxydibenzoylmethane, 2,6-dimethyl-4-tert-butyl-4'- methoxydibenzoylmethane, 1-(4-tert-butylphenyl)-3-(2-hydroxyphenyl)propane-1,3-dione, 1-(4-methoxy-1-benzofuran-5-yl)-3-phenylpropane-1 ,3-dione; preferably chosen, alone or as a mixture, from 4-tert-butyl-4'-methoxydibenzoylmethane and/or 4-isopropyldibenzoylmethane; preferably chosen from 4-tert-butyl-4'-methoxydibenzoylmethane.

By way of example, 4-isopropyldibenzoylmethane is sold under the name "EUSOLEX 9020" by the company MERCK, and 4-tert-butyl-4'-methoxydibenzoylmethane or butyl methoxy dibenzoylmethane, of formula:
[form 7]

is sold under the name “PARSOL 1789” by the company DSM Nutritional Products.

Also by way of example, 1-(4-methoxy-1-benzofuran-5-yl)-3-phenylpropane-1,3-dione, of formula:
[form 8]
.

According to a particularly preferred embodiment, the composition in accordance with the invention comprises 4-tert-butyl-4'-methoxydibenzoylmethane (INCI name: butyl methoxy dibenzoylmethane).

When they are present, the content of the compound(s) derived from dibenzoylmethane is between 0.1 and 15% by weight, preferably between 0.2 and 10% by weight, more preferably between 0.3 and 5% by weight. , relative to the total weight of the composition.

ADDITIONAL ACRYLIC POLYMER

According to a particular embodiment of the invention, the composition comprises at least one polymer comprising monomer units of formulas (A) and (B) defined below:
[form A] [form B]

in which :
R1, independently of one another, is chosen from alkyl or alkylene radicals, and
at least 60% by weight of the R1 groups are radicals chosen from stearyl and behenyl radicals, the percentage by weight relating to the sum of all the R1 groups present in the polymer, and
the weight ratio of the sum of all hydroxyethyl acrylate units to the sum of all acrylate units carrying the R1 group ranges from 1:30 to 1:1,
and the sum of the total of units A and B is at least 95% by weight of the total weight of the polymer.

Preferably, R1 consists of alkyl radicals, preferably of C16-C22 alkyl radicals, and more preferably of stearyl radicals (at C18) or behenyl radicals (at C22).

Preferably, at least 70% by weight of the R1 groups are stearyl or behenyl radicals, preferably at least 80% by weight, more preferably at least 90% by weight.

According to a preferred embodiment, all the R1 groups are behenyl radicals.

According to another preferred embodiment, all the R1 groups are stearyl radicals.

Preferably, said weight ratio ranges from 1:15 to 1:1, preferably ranges from 1:10 to 1:4.

Advantageously, the polymer units present in the polymer consist of the units (A) and (B) described previously.

The polymer has a number-average molecular weight Mn ranging from 2000 to 9000 g/mol, preferably ranging from 5000 to 9000 g/mol. The number-average molecular weight can be measured with the gel permeation chromatography method, for example according to the method described in the example below.

Preferably, the polymer has a melting temperature ranging from 40°C to 70°C, and preferentially ranging from 45°C to 67°C. The melting temperature is measured by differential scanning calorimetry (or DSC: Differential Scanning Calorimetry), for example according to the method described in the example below.

According to a first embodiment, when the polymer is such that at least 60% by weight of the R1 groups are stearyl radicals, then the polymer preferably has a melting point ranging from 40 to 60° C., and preferentially ranging from 45 to 55°C.

According to a second embodiment, when the polymer is such that at least 60% by weight of the R1 groups are behenyl radicals, then the polymer has a melting point ranging from 60° C. to 70° C., and preferably ranging from 63°C to 67°C.

The polymer used according to the invention can be prepared by polymerization of monomer of formula
CH2=CH-COO-R1, R1 having the meaning described above, and 2-hydroxyethyl acrylate.

The polymerization can be carried out according to known methods, such as polymerization in solution or in emulsion.

The polymerization is for example described in document US 2007/0264204.

The acrylic polymer(s) as defined above may be present in the composition according to the invention in an active material content ranging from 0.05 to 10% by weight, relative to the total weight of the composition, preferably ranging from 0 1 to 5% by weight and better still ranging from 0.2 to 3% by weight.

FAT PHASE

The composition in accordance with the invention may comprise at least one fatty phase.

For the purposes of the invention, the term "fatty phase" means a phase comprising at least one fatty substance, in particular liquid, solid or pasty, and all the liposoluble and lipophilic ingredients used for the formulation of the compositions of the invention.

According to a particular embodiment, the composition according to the invention comprises at least one oil.

By oil is meant any fatty substance in liquid form at room temperature (20 – 25°C) and at atmospheric pressure (760 mm Hg).

The fatty phase may in particular comprise at least one volatile or non-volatile hydrocarbon-based oil and/or a volatile and or non-volatile silicone oil and/or a volatile and or non-volatile fluorinated oil.

Within the meaning of the present invention, the term “silicone oil” means an oil comprising at least one silicon atom, and in particular at least one Si—O group.

The term "hydrocarbon oil" means an oil containing mainly hydrogen and carbon atoms and optionally one or more heteroatoms, in particular nitrogen and oxygen. Thus these oils may in particular contain one or more carboxy, ester, ether or hydroxy functions.

The term "fluorinated oil" means an oil comprising at least one fluorine atom.

By “volatile oil” is meant, within the meaning of the invention, an oil capable of evaporating on contact with the skin or the keratin fiber in less than one hour, at ambient temperature and atmospheric pressure. The volatile oil or oils of the invention are volatile cosmetic oils, liquid at room temperature, having a non-zero vapor pressure, at room temperature and atmospheric pressure, ranging in particular from 0.13 Pa to 40,000 Pa (10 ^{- 3} to 300 mm Hg), in particular ranging from 1.3 Pa to 13,000 Pa (0.01 to 100 mm Hg), and more particularly ranging from 1.3 Pa to 1300 Pa (0.01 to 10 mm of Hg).

By "non-volatile oil" is meant an oil remaining on the skin or the keratin fiber at room temperature and atmospheric pressure for at least several hours and having in particular a vapor pressure of less than 10 ^-3 mm Hg (0.13 Pa) .

Hydrocarbon oils

The composition in accordance with the invention may comprise at least one ester of a C2-C22 di or tricarboxylic acid and of C1-C24 alcohols.

The C ₂ -C ₂₂ di or tricarboxylic acids are chosen in particular from citric acid, malic acid, malonic acid, succinic, adipic, maleic, fumaric, tartaric or isocitric acid and mixtures thereof. Preferably the acids are citric acid and adipic acid, and even more preferably it is citric acid.

C1-C24 alcohols are not oxyalkylenated. They can be aliphatic, cyclic or aromatic, having 1 to 24 carbon atoms. They are chosen in particular from phenol, benzyl alcohol, lauryl alcohol, myristyl alcohol, cetyl alcohol, stearyl alcohol, methanol, ethanol, propanol, n-butanol, t -butanol, pentanol, hexanol. Preferably, the alcohol or alcohols are C1-C6 and can be chosen from methanol, ethanol, propanol, n-butanol, t-butanol, pentanol, hexanol, and even more preferentially they are it's ethanol.

The ester(s) of C2-C22 di or tricarboxylic acid and of C1-C24 alcohols can be mono- or poly-esterified.

By monoesterified is meant that only one of the two or three carboxylic acid functions is esterified. By polyesterified is meant that at least two carboxylic acid functions are esterified.

The di or tricarboxylic acid can be esterified by several different alcohols. Preferably, it is esterified with a single alcohol.

According to a particular embodiment of the invention, the composition comprises at least one ester of a C3-C22 tricarboxylic acid and of C1-C24, preferably C1-C6, alcohols. This or these esters can be mono-, di- or tri-esterified.

By mono-esterified is meant that only one of the three carboxylic acid functions is esterified. By di-esterified is meant that two carboxylic acid functions out of the three are esterified. By tri-esterified is meant that the three carboxylic acid functions are esterified.

According to a particular embodiment of the invention, the ester(s) of C3-C22 tricarboxylic acid and of C1-C6 alcohols are tri-esterified.

According to a particular embodiment of the invention, the ester(s) of C3-C22 tricarboxylic acid and of C1-C6 alcohols are chosen from the compounds of formula (9) below:
(R ₁ O-CO)CH ₂ -C(R)(OC-OR ₂ )-CH ₂ (OC-OR ₃ )
in which :
R1, R2 and R3 represent, independently of each other, a hydrogen atom or a monovalent, saturated or unsaturated, aliphatic, cyclic or aromatic hydrocarbon group having from 1 to 6 carbon atoms;
R represents a hydrogen atom or a hydroxyl radical.

According to a preferred embodiment, R1, R2 and R3 represent, independently of each other, a hydrogen atom or an alkyl radical, linear or branched, substituted or unsubstituted, preferably unsubstituted, C1-C6, and particular a radical chosen from methyl, ethyl, propyl, n-butyl, t-butyl, pentyl, hexyl radicals. Preferably, R1, R2 and R3 are chosen independently of each other from a hydrogen atom and the methyl, ethyl, propyl, n-butyl and t-butyl radicals.

According to a preferred embodiment of the invention, the radicals R1, R2 and R3 are identical and are chosen from C1-C6 alkyl radicals, preferably C1-C4 alkyl radicals, and even more preferably they are ethyl radicals. .

According to a preferred embodiment of the invention, R represents a hydroxyl radical.

According to a particular embodiment of the invention, the ester of tricarboxylic acid and C1-C6 alcohols has the following formula:
[Formula 10]

As an example of a C3-C22 tricarboxylic acid ester and C1-C6 alcohols of formula (10) and INCI name TRIETHYL CITRATE, mention will be made of that which is marketed under the name CITROFOL AI EXTRA by the company JUNGBUNZLAUER.

As non-volatile hydrocarbon-based oils which can be used according to the invention, mention may also be made of:
(i) hydrocarbon oils of vegetable origin such as triesters of glycerides which are generally triesters of fatty acids and of glycerol whose fatty acids can have chain lengths varying from C ₄ to C ₂₄ , the latter possibly be linear or branched, saturated or unsaturated; these oils are in particular wheat germ, sunflower, grapeseed, sesame, corn, apricot, castor, shea, avocado, olive, soybean oil, sweet almond, palm, rapeseed, cotton, hazelnut, macadamia, jojoba, alfalfa, poppy, pumpkin, sesame, squash, rapeseed, blackcurrant, evening primrose, millet, barley, quinoa, rye, safflower, bankoulier, passionflower, muscat rose; or alternatively caprylic/capric acid triglycerides such as those sold by the company Stéarineries Dubois or those sold under the names Miglyol 810®, 812® and 818® by the company Dynamit Nobel;
(ii) synthetic ethers having 10 to 40 carbon atoms;
(iii) linear or branched hydrocarbons, of mineral or synthetic origin such as petroleum jelly, polydecenes, hydrogenated polyisobutene such as parleam, squalane, and mixtures thereof;
(iv) synthetic esters such as oils of formula RCOOR' in which R represents the residue of a linear or branched fatty acid containing from 1 to 40 carbon atoms and R' represents a hydrocarbon chain in particular branched containing from 1 to 40 carbon atoms provided that R + R' is ≥ 10, such as Purcellin's oil (cetostearyl octanoate), isopropyl myristate, isopropyl palmitate, benzoate of C ₁₂ -C alcohols ₁₅ as the product sold under the trade name "Finsolv TN®" or "Witconol TN®" by the company WITCO or "TEGOSOFT TN ®" by the company EVONIK GOLDSCHMIDT, 2-ethylphenyl benzoate as the commercial product sold under the name “X-TEND 226®” by ISP Company, Isopropyl Lanolate, Hexyl Laurate, Diisopropyl Adipate, Isononyl Isononanoate, Oleyl Erucate, 2-Ethyl Palmitate -hexyl, isostearyl isostearate, diisopropyl sebacate such as the product sold under the name "Dub Dis" by the company Stearinerie Dubois, octanoates, decanoates or ricinoleates of alcohols or polyalcohols such as propylene dioctanoate glycol; hydroxylated esters such as isostearyl lactate, di-isostearyl malate; and pentaerythritol esters; citrates or tartrates such as linear C ₁₂ -C ₁₃ di-alkyl tartrates such as those sold under the name COSMACOL ETI® by the company ENICHEM AUGUSTA INDUSTRIALE as well as linear C ₁₄ -C ₁₅ di-alkyl tartrates such as than those sold under the name COSMACOL ETL® by the same company; acetates;
(v) fatty alcohols which are liquid at room temperature with a branched and/or unsaturated carbon chain having from 12 to 26 carbon atoms such as octyl dodecanol, isostearyl alcohol, oleyl alcohol, 2-hexyldecanol, 2- butyloctanol, 2-undecylpentadecanol;
(vi) higher C12-C22 fatty acids, such as oleic acid, linoleic acid, linolenic acid;
(vii) carbonates such as dicaprylyl carbonate such as the product sold under the name “Cetiol CC®” by the company Cognis;
and their mixtures.

Among the non-volatile hydrocarbon-based oils which can be used according to the invention, preference will be given more particularly to glyceride triesters and in particular the triglycerides of caprylic/capric acids, synthetic esters and in particular diisopropyl adipate, diisopropyl sebacate, isopropyl palmitate, dicaprylyl carbonate, isononyl isononanoate, oleyl erucate, C ₁₂ -C ₁₅ alcohol benzoate, 2-ethylphenyl benzoate and fatty alcohols, in particular octyldodecanol. Preferably, the non-volatile hydrocarbon oils are chosen from diisopropyl adipate, diisopropyl sebacate, isopropyl palmitate, dicaprylyl carbonate.

As volatile hydrocarbon-based oils that can be used according to the invention, mention may in particular be made of hydrocarbon-based oils having from 8 to 16 carbon atoms, and in particular branched C alkanes₈-VS₁₆like C isoalkanes₈-VS₁₆of petroleum origin (also called isoparaffins) such as isododecane (also called 2,2,4,4,6-pentamethylheptane), isodecane, isohexadecane, the oils sold under the trade names Isopars or Permetyls, the C-branched esters₈-VS₁₆, iso-hexyl neopentanoate, and mixtures thereof.

Mention may also be made of the alkanes described in the patent applications of the company Cognis WO 2007/068371, or WO2008/155059 (mixtures of distinct alkanes and different from at least one carbon). These alkanes are obtained from fatty alcohols, themselves obtained from copra or palm oil. mention may be made of the mixtures of n-undecane (C ₁₁ ) and n-tridecane (C ₁₃ ) obtained in examples 1 and 2 of application WO2008/155059 from the company Cognis. Mention may also be made of n-dodecane (C ₁₂ ) and n-tetradecane (C ₁₄ ) sold by Sasol respectively under the references PARAFOL 12-97 and PARAFOL 14-97®, as well as their mixtures.

Other volatile hydrocarbon-based oils such as petroleum distillates, in particular those sold under the name Shell Solt® by the company SHELL, can also be used. According to one embodiment, the volatile solvent is chosen from volatile hydrocarbon oils having from 8 to 16 carbon atoms and their mixtures.

Silicone oils

The non-volatile silicone oils can be chosen in particular from non-volatile polydimethylsiloxanes (PDMS), polydimethylsiloxanes comprising alkyl or alkoxy groups, pendent and/or at the end of the silicone chain, groups each having from 2 to 24 carbon atoms, silicones phenyl such as phenyl trimethicones, phenyl dimethicones, phenyl trimethylsiloxy diphenylsiloxanes, diphenyl dimethicones, diphenyl methyldiphenyl trisiloxanes, 2-phenylethyl trimethylsiloxysilicates.

As volatile silicone oils, mention may be made, for example, of volatile linear or cyclic silicone oils, in particular those having a
viscosity ≤ 8 centistokes (8 10 ^-6 m ² /s), and having in particular from 2 to 7 silicon atoms, these silicones optionally comprising alkyl or alkoxy groups having from 1 to 10 carbon atoms. As volatile silicone oil which can be used in the invention, mention may in particular be made of octamethyl cyclotetrasiloxane, decamethyl cyclopentasiloxane, dodecamethyl cyclohexasiloxane, heptamethyl hexyltrisiloxane, heptamethyloctyl trisiloxane, hexamethyl disiloxane, octamethyl trisiloxane, decamethyl tetrasiloxane, dodecamethyl pentasiloxane and mixtures thereof.

A fatty phase according to the invention may also comprise, mixed with or dissolved in oil, other fatty substances.

Another fatty substance which may be present in the fatty phase may be, for example:
- a fatty acid chosen from fatty acids comprising from 8 to 30 carbon atoms, such as stearic acid, lauric acid, palmitic acid and oleic acid;
- a wax chosen from waxes such as lanolin, beeswax, carnauba or candelilla wax, rice bran wax, paraffin or lignite waxes or microcrystalline waxes, ceresin or ozokerite , synthetic waxes such as polyethylene waxes, Fischer-Tropsch waxes;
- a gum chosen from silicone gums (dimethiconol),
- a pasty compound, such as polymeric or non-polymeric silicone compounds, esters of an oligomeric glycerol, arachidyl propionate, fatty acid triglycerides and their derivatives,
- and mixtures thereof.

Preferably, the overall fatty phase, including all the lipophilic substances other than the lipophilic screening agents of the composition capable of being dissolved in this same phase, represents from 5 to 95% by weight, and preferably from 10 to 80% by weight. weight relative to the total weight of the composition.

AQUEOUS PHASE

The composition in accordance with the invention may comprise at least one aqueous phase.

The aqueous phase contains water, and optionally other water-soluble or water-miscible organic solvents.

An aqueous phase suitable for the invention may comprise, for example, water chosen from natural spring water, such as water from La Roche-Posay, water from Vittel, water from Saint Gervais Mont Blanc, or Vichy waters, or a floral water.

According to a particular form of the invention, the overall aqueous phase, including all the hydrophilic substances of the composition capable of being dissolved in this same phase, represents from 1 to 99% by weight, and preferably from 10 to 80% by weight. weight relative to the total weight of the composition.

ADDITIVES

Additional UV filters

The compositions according to the invention may also contain one or more complementary UV filters chosen from hydrophilic, lipophilic or insoluble organic UV filters and/or one or more mineral pigments. Preferably, it will consist of at least one hydrophilic, lipophilic or insoluble organic UV filter.

By "hydrophilic UV filter" is meant any cosmetic or dermatological organic or inorganic compound filtering UV radiation capable of being completely dissolved in the molecular state in a liquid aqueous phase or else of being dissolved in colloidal form (for example in the form micellar) in a liquid aqueous phase.

By "lipophilic filter" is meant any cosmetic or dermatological organic or inorganic compound filtering UV radiation capable of being completely dissolved in the molecular state in a liquid fatty phase or else of being dissolved in colloidal form (for example in micellar form ) in a liquid fatty phase.

By "insoluble UV filter" is meant any cosmetic or dermatological organic or inorganic compound filtering UV radiation having a solubility in water of less than 0.5% by weight and a solubility of less than 0.5% by weight in most organic solvents such as paraffin oil, fatty alcohol benzoates and fatty acid triglycerides, for example Miglyol 812® marketed by the company DYNAMIT NOBEL. This solubility, achieved at 70°C, is defined as the quantity of product in solution in the solvent at equilibrium with an excess of solid in suspension after returning to ambient temperature. It can easily be assessed in the laboratory.

The complementary organic UV screening agents are chosen in particular from cinnamic compounds; anthranilate compounds; salicylic compounds, benzylidenecamphor compounds; benzophenone compounds; β,β-diphenylacrylate compounds; triazine compounds; benzotriazole compounds; benzalmalonate compounds, in particular those cited in US Pat. No. 5,624,663; benzimidazole derivatives; imidazoline compounds; bis-benzoazolyl compounds as described in patents EP669323 and US 2,463,264; p-aminobenzoic compounds (PABA); methylene bis-(hydroxyphenyl benzotriazole) compounds as described in applications US5,237,071, US 5,166,355, GB2303549, DE 197 26 184 and EP893119; benzoxazole compounds as described in patent applications EP0832642, EP1027883, EP1300137 and DE10162844; screening polymers and screening silicones such as those described in particular in application WO-93/04665; dimers derived from α-alkylstyrene such as those described in patent application DE19855649; 4,4-diarylbutadiene compounds as described in applications EP0967200, DE19746654, DE19755649, EP-A-1008586, EP1133980 and EP133981 and mixtures thereof.

Examples of organic photoprotective agents include those designated below by their INCI name.

Cinnamic compounds:
Ethylhexyl Methoxycinnamate sold in particular under the trade name PARSOL MCX ® by DSM Nutritial Products
Isopropyl Methoxycinnamate
Isoamyl p-Methoxycinnamate sold under the trade name NEO HELIOPAN E 1000 ® by Symrise
DEA Methoxycinnamate,
Diisopropyl Methylcinnamate,
Glyceryl Ethylhexanoate Dimethoxycinnamate.

Para-aminobenzoic compounds :
PABA,
Ethyl PABA,
Ethyl Dihydroxypropyl PABA,
Ethylhexyl Dimethyl PABA sold in particular under the name "ESCALOL 507®" by ISP,
Glyceryl PABA,
PEG-25 PABA sold under the name "UVINUL P 25®" by BASF.

Salicylic compounds:
Homosalate sold under the name "Eusolex HMS®" by Rona/EM Industries,
Ethylhexyl Salicylate sold under the name “NEO HELIOPAN OS®” by Symrise,
Dipropylene glycol Salicylate sold under the name "DIPSAL ®" by SCHER,
TEA Salicylate, sold under the name “NEO HELIOPAN TS®” by Symrise.

Compounds β , β - diphenylacrylate :
Octocrylene sold in particular under the trade name "UVINUL N 539®" by BASF,
Etocrylene, sold in particular under the trade name “UVINUL N 35®” by BASF.

Benzophenone compounds:
Benzophenone-1 sold under the trade name “UVINUL 400®” by BASF,
Benzophenone-2 sold under the trade name “UVINUL D 50®” by BASF,
Benzophenone-3 or Oxybenzone, sold under the trade name “UVINUL M 40®” by BASF,
Benzophenone-4 sold under the trade name “UVINUL MS 40®” by BASF,
Benzophenone-5,
Benzophenone-6 sold under the trade name “Helisorb 11®” by Norquay,
Benzophenone-8 sold under the trade name “Spectra-Sorb UV-24®” by American Cyanamid,
Benzophenone-9 sold under the trade name “UVINUL DS 49®” by BASF,
Benzophenone-12,
n-hexyl 2-(4-diethylamino-2-hydroxybenzoyl)-benzoate sold under the trade name "UVINUL A Plus ®" or in a mixture with octylmethoxycinnamate under the trade name "UVINUL A Plus B®" by the company BASF ,
1,1'-(1,4-piperazinediyl)bis[1-[2-[4-(diethylamino)-2-hydroxybenzoyl]phenyl]-methanone (CAS 919803-06-8) as described in application WO2007/ 071584; this compound being advantageously used in micronized form (average size of 0.02 to 2 μm) which can be obtained for example according to the micronization process described in applications GB-A-2 303 549 and EP-A-893119 and in particular in the form of aqueous dispersion.

Benzylidene Camphor Compounds :
3-Benzylidene camphor manufactured under the name “MEXORYL SD®” by CHIMEX,
4-Methylbenzylidene camphor sold under the name “EUSOLEX 6300®” by MERCK,
Benzylidene Camphor Sulfonic Acid manufactured under the name “MEXORYL SL®” by CHIMEX,
Camphor Benzalkonium Methosulfate manufactured under the name “MEXORYL SO®” by CHIMEX,
Terephthalylidene Dicamphor Sulfonic Acid manufactured under the name “MEXORYL SX®” by CHIMEX,
Polyacrylamidomethyl Benzylidene Camphor manufactured under the name “MEXORYL SW®” by CHIMEX.

Compounds phenyl benzimidazole :
Phenylbenzimidazole Sulfonic Acid sold in particular under the trade name “EUSOLEX 232®” by MERCK.

Bis- benzoazolyl compounds :
Disodium Phenyl Dibenzimidazole Tetra-sulfonate sold under the trade name “NEO HELIOPAN AP®” by Haarmann and REIMER.

Compounds phenyl benzotriazole :
Drometrizole Trisiloxane sold under the name “Silatrizole®” by RHODIA CHIMIE.

Methylene bis-( compounds hydroxyphenyl benzotriazole ):
Methylene bis-Benzotriazolyl Tetramethylbutylphenol, in particular in solid form such as the product sold under the trade name "MIXXIM BB/100 ®" by FAIRMOUNT CHEMICAL or in the form of an aqueous dispersion of micronized particles having an average particle size which varies from 0.01 to 5 μm and more preferably from 0.01 to 2 μm and more particularly from 0.020 to 2 μm with at least one alkylpolyglycoside surfactant of structure C_notH_2n+1O(C₆H₁₀O₅)_xH in which n is an integer from 8 to 16 and x is the average degree of polymerization of the unit (C₆H₁₀O₅) and varies from 1.4 to 1.6 as described in patent GB-A-2 303 549 in particular sold under the trade name "TINOSORB M®" by BASF or in the form of an aqueous dispersion of micronized particles having an average size of the particles which varies from 0.02 to 2 μm and more preferentially from 0.01 to 1.5 μm and more particularly from 0.02 to 1 μm in the presence of at least one mono-(C₈-VS₂₀) polyglycerol alkyl ester having a degree of glycerol polymerization of at least 5 such as the aqueous dispersions described in application WO2009/063392.

Triazine compounds:
- 3,3'-(1,4-Phenylene)bis(5,6-diphenyl-1,2,4-triazine), INCI name Phenylene Bis-Diphenyl triazine, with the following chemical formula:
[form 11]

- Bis-Ethylhexyloxyphenol Methoxyphenyl Triazine sold under the trade name “TINOSORB S®” by BASF,
- Ethylhexyl Triazone sold in particular under the trade name “UVINUL T 150®” by BASF,
- Diethylhexyl Butamido Triazone sold under the trade name "UVASORB HEB ®" by SIGMA 3V,
- 2,4,6-tris-(4'-amino dineopentyl benzalmalonate)-s-triazine,
- 2,4,6-tris-(4'-amino benzalmalonate diisobutyl)-s-triazine,
- 2,4-bis-(4'-aminobenzoate of n-butyl)-6-(aminopropyltrisiloxane)-s-triazine,
- 2,4-bis-(4'-aminobenzalmalonate of dineopentyl)-6-(4'-aminobenzoate of n-butyl)-s-triazine,
- symmetrical triazine filters substituted with naphthalenyl groups or polyphenyl groups described in patent US6,225,467, application WO2004/085412 (see compounds 6 and 9) or the document "Symmetrical Triazine Derivatives" IP.COM IPCOM000031257 Journal, INC WEST HENRIETTA, NY, US (September 20, 2004) in particular 2,4,6-tris(di-phenyl)-triazine and 2,4,6-tris(ter-phenyl)-triazine which is included in the patent applications WO06/035000, WO06/034982, WO06/034991, WO06/035007, WO2006/034992, WO2006/034985, these compounds being advantageously used in micronized form (average particle size from 0.02 to 3 μm) obtainable for example according to the micronization process described in applications GB-A-2 303 549 and EP-A-893119 and in particular in aqueous dispersion form,
- triazine silicones substituted with two aminobenzoate groups as described in patent EP0841341, in particular 2,4-bis-(n-butyl 4'-aminobenzalmalonate)-6-[(3-{1,3,3,3- tetramethyl-1-[(trimethylsilyloxy]disiloxanyl}propyl)amino]-s-triazine.

Anthranil compounds :
Menthyl anthranilate sold under the trade name "NEO HELIOPAN MA®" by Symrise.

Imidazoline compounds:
Ethylhexyl Dimethoxybenzylidene Dioxoimidazoline Propionate.

Benzalmalonate compounds :
Polyorganosiloxane with benzalmalonate functions such as Polysilicone-15 sold under the trade name “PARSOL SLX®” by HOFFMANN LA ROCHE.

4,4-diarylbutadiene compounds:
-1,1-dicarboxy (2,2'-dimethyl-propyl)-4,4-diphenylbutadiene.

Benzoxazole compounds :
2,4-bis-[5-1(dimethylpropyl)benzoxazol-2-yl-(4-phenyl)-imino]-6-(2-ethylhexyl)-imino-1,3,5-triazine sold as 'Uvasorb K2A® by Sigma 3V.

The preferred organic filters are chosen from:
Ethylhexyl Methoxycinnamate,
Ethylhexyl Salicylate,
Homosalate,
Octocrylene,
Phenylbenzimidazole Sulphonic Acid,
Benzophenone-3,
Benzophenone-4,
Benzophenone-5,
n-hexyl 2-(4-diethylamino-2-hydroxybenzoyl)-benzoate,
4-Methylbenzylidene camphor,
Terephthalylidene Dicamphor Sulfonic Acid,
Disodium Phenyl Dibenzimidazole Tetra-sulfonate,
Methylene bis-Benzotriazolyl Tetramethylbutylphenol,
Bis-Ethylhexyloxyphenol Methoxyphenyl Triazine
Ethylhexyl Triazone,
Diethylhexyl Butamido Triazone,
2,4,6-tris-(4'-amino dineopentyl benzalmalonate)-s-triazine,
2,4,6-tris-(diisobutyl 4'-amino benzalmalonate)-s-triazine,
2,4-bis-(n-butyl 4'-aminobenzoate)-6-(aminopropyltrisiloxane)-s-triazine,
2,4-Bis-(Dineopentyl 4'-aminobenzalmalonate)-6-(n-Butyl 4'-aminobenzoate)-s-triazine,
2,4-bis-(n-butyl 4'-aminobenzalmalonate)-6-[(3-{1,3,3,3-tetramethyl-1-[(trimethylsilyloxy]disiloxanyl}propyl)amino]-s-triazine,
2,4,6-tris-(di-phenyl)-triazine,
2,4,6-tris-(ter-phenyl)-triazine
Drometrizole Trisiloxane,
Polysilicon-15,
1,1-dicarboxy (2,2'-dimethyl-propyl)-4,4-diphenylbutadiene,
2,4-bis-[5-1(dimethylpropyl)benzoxazol-2-yl-(4-phenyl)-imino]-6-(2-ethylhexyl)-imino-1,3,5-triazine,
and their mixtures.

The particularly preferred organic screening agents are chosen from:
Ethylhexyl Salicylate,
Homosalate,
Octocrylene,
n-hexyl 2-(4-diethylamino-2-hydroxybenzoyl)-benzoate,
Terephthalylidene Dicamphor Sulfonic Acid,
Bis-Ethylhexyloxyphenol Methoxyphenyl Triazine,
Ethylhexyl Triazone,
Diethylhexyl Butamido Triazone,
2,4-bis-(n-butyl 4'-aminobenzalmalonate)-6-[(3-{1,3,3,3-tetramethyl-1-[(trimethylsilyloxy]disiloxanyl}propyl)amino]-s-triazine,
Drometrizole Trisiloxane,
and their mixtures.

The inorganic UV filters used in accordance with the present invention are metal oxide pigments. More preferably, the inorganic UV screening agents of the invention are metal oxide particles having an average elementary particle size less than or equal to 0.5 μm, more preferably between 0.005 and 0.5 μm and even more preferably between 0.01 and 0.2 μm, even better between 0.01 and 0.1 μm, and more particularly between 0.015 and 0.05 μm.

They can be chosen in particular from titanium, zinc, iron, zirconium and cerium oxides or mixtures thereof.

Such coated or uncoated metal oxide pigments are described in particular in patent application EP-A-0 518 773. As commercial pigments, mention may be made of the products sold by the companies SACHTLEBEN PIGMENTS, TAYCA, MERCK AND DEGUSSA .

Metal oxide pigments can be coated or uncoated.

Coated pigments are pigments which have undergone one or more surface treatments of a chemical, electronic, mechanochemical and/or mechanical nature with compounds such as amino acids, beeswax, fatty acids, fatty alcohols, anionic surfactants, lecithins, sodium, potassium, zinc, iron or aluminum salts of fatty acids, metal alkoxides (titanium or aluminum), polyethylene, silicones, proteins (collagen, elastin) , alkanolamines, silicon oxides, metal oxides or sodium hexametaphosphate.

The coated pigments are more particularly coated titanium oxides:
- silica such as the "SUNVEIL®" product from IKEDA,
- silica and iron oxide such as the "SUNVEIL F®" product from IKEDA,
- silica and alumina such as the products "MICROTITANIUM DIOXIDE MT 500 SA®" and "MICROTITANIUM DIOXIDE MT 100 SA" from the company TAYCA, "TIOVEIL" from the company TIOXIDE,
- alumina such as the products "TIPAQUE TTO-55 (B)®" and "TIPAQUE TTO-55 (A)®" from ISHIHARA, and "UVT 14/4" from SACHTLEBEN PIGMENTS,
- alumina and aluminum stearate such as the products "MICROTITANIUM DIOXIDE MT 100 T®, MT 100 TX®, MT 100 Z®, MT-01®" from the company TAYCA, the products "Solaveil CT-10 W ®" and "Solaveil CT 100®" from UNIQEMA and the product "Eusolex T-AVO®" from MERCK,
- silica, alumina and alginic acid such as the product "MT-100 AQ®" from the company TAYCA,
- alumina and aluminum laurate such as the product "MICROTITANIUM DIOXIDE MT 100 S®" from the company TAYCA,
- iron oxide and iron stearate such as the product "MICROTITANIUM DIOXIDE MT 100 F®" from the company TAYCA,
- zinc oxide and zinc stearate such as the product "BR 351®" from the company TAYCA,
- silica and alumina and treated with a silicone such as the products "MICROTITANIUM DIOXIDE MT 600 SAS®", "MICROTITANIUM DIOXIDE MT 500 SAS®" or "MICROTITANIUM DIOXIDE MT 100 SAS®" from the company TAYCA,
- silica, alumina, aluminum stearate and treated with a silicone such as the product "STT-30-DS®" from TITAN KOGYO,
- silica and treated with a silicone such as the product "UV-TITAN X 195®" from the company SACHTLEBEN PIGMENTS,
- alumina and treated with a silicone such as the products "TIPAQUE TTO-55 (S)®" from ISHIHARA, or "UV TITAN M 262®" from SACHTLEBEN PIGMENTS,
- triethanolamine such as the product "STT-65-S" from TITAN KOGYO,
- stearic acid such as the product "TIPAQUE TTO-55 (C)®" from ISHIHARA,
- sodium hexametaphosphate such as the product "MICROTITANIUM DIOXIDE MT 150 W®" from the company TAYCA.
- TiO ₂ treated with octyl trimethyl silane sold under the trade name "T 805®" by the company DEGUSSA SILICES,
- TiO ₂ treated with a polydimethylsiloxane sold under the trade name "70250 Cardre UF TiO2SI3®" by the company CARDRE,
- anatase/rutile TiO ₂ treated with a polydimethylhydrogensiloxane sold under the trade name "MICRO TITANIUM DIOXIDE USP GRADE HYDROPHOBIC®" by the company COLOR TECHNIQUES,
- TiO ₂ coated with triethylhexanoin, aluminum stearate, alumina sold under the trade name Solaveil CT-200-LQ-(WD) from CRODA,
- TiO ₂ coated with aluminum stearate, alumina and silicone sold under the trade name Solaveil CT-12W-LQ- (WD from CRODA),
- the TiO ₂ coated with lauroyl lysine sold by Daito Kasei Kogyo under the name LL 5 Titanium Dioxyde CR 50,
- TiO ₂ coated with C9-15 fluoroalcohol phosphate and aluminum hydroxide sold by Daito Kasei Kogyo under the name PFX-5 TiO2 CR-50.

Mention may also be made of TiO ₂ pigments doped with at least one transition metal such as iron, zinc, manganese and more particularly manganese. Preferably, said doped pigments are in the form of an oily dispersion. The oil present in the oily dispersion is preferably chosen from triglycerides, including those of capric/caprylic acids. The oily dispersion of titanium oxide particles may additionally comprise one or more dispersing agents such as, for example, a sorbitan ester such as sorbitan isostearate, a polyoxyalkylenated fatty acid and glycerol ester such as TRI-PPG3 MYRISTYLETHER CITRATE and POLYGLYCERYL-3 POLYRICINOLEATE. Preferably, the oily dispersion of titanium oxide particles comprises at least one dispersing agent chosen from polyoxyalkylenated fatty acid and glycerol esters. Mention may be made more particularly of the oily dispersion of particles of TiO ₂ doped with manganese in the triglyceride of capric/caprylic acid in the presence of TRI-PPG-3 MYRISTYLETHER CITRATE and POLYGLYCERYL-3-POLYRICINOLEATE and SORBITAN ISOSTERATE with the INCI name: TITANIUM DIOXIDE (and) TRI-PPG-3 MYRISTYLETHER CITRATE (and) POLYGLYCERYL-3 RICINOLEATE (and) SORBITAN ISOSTEARATE like the product sold under the trade name OPTISOL TD50 ® by the company CRODA.

The uncoated titanium oxide pigments are for example sold by the company TAYCA under the trade names "MICROTITANIUM DIOXIDE MT 500 B" or "MICROTITANIUM DIOXIDE MT600 B®", by the company DEGUSSA under the name "P 25", by the company WACKHER under the name "Transparent titanium oxide PW®", by the company MIYOSHI KASEI under the name "UFTR®", by the company TOMEN under the name "ITS®" and by the company TIOXIDE under the name "TIOVEIL AQ ".

Uncoated zinc oxide pigments are, for example:
- those marketed under the name "Z-cote" by the company Sunsmart;
- those marketed under the name "Nanox®" by the company Elementis;
- those marketed under the name "Nanogard WCD 2025®" by the company Nanophase Technologies.

Examples of coated zinc oxide pigments are:
- those marketed under the name "Oxide zinc CS-5®" by the company Toshibi (ZnO coated with polymethylhydrogensiloxane);
- those marketed under the name "Nanogard Zinc Oxide FN®" by the company Nanophase Technologies (dispersed at 40% in Finsolv TN®, C12-C15 alcohol benzoate);
- those marketed under the name "DAITOPERSION Zn-30®" and "DAITOPERSION Zn-50®" by the company Daito (dispersions in cyclopolymethylsiloxane/oxyethylenated polydimethylsiloxane, containing 30% or 50% of zinc oxides coated with silica and polymethylhydrogensiloxane);
- those marketed under the name “NFD Ultrafine ZnO®” by the company Daikin (ZnO coated with perfluoroalkyl phosphate and copolymer based on perfluoroalkylethyl in dispersion in cyclopentasiloxane);
- those marketed under the name "SPD-Z1®" by the company Shin-Etsu (ZnO coated with silicone-grafted acrylic polymer, dispersed in cyclodimethylsiloxane);
- those marketed under the name “Escalol Z100®” by the company ISP (ZnO treated with alumina and dispersed in the ethylhexyl methoxycinnamate/PVP-hexadecene/methicone copolymer mixture);
- those marketed under the name "Fuji ZnO-SMS-10®" by the company Fuji Pigment (ZnO coated with silica and polymethylsilsesquioxane);
- those marketed under the name "Nanox Gel TN®" by the company Elementis (ZnO dispersed at 55% in C12-C15 alcohol benzoate with polycondensate of hydroxystearic acid).

The uncoated cerium oxide pigments can be, for example, those sold under the name “COLLOIDAL CERIUM OXIDE®” by the company RHONE POULENC.

Uncoated iron oxide pigments are for example sold by the company ARNAUD under the names "NANOGARD WCD 2002® (FE 45B®)", "NANOGARD IRON FE 45 BL AQ", "NANOGARD FE 45R AQ®, "NANOGARD WCD 2006 ® (FE 45R®)", or by the company MITSUBISHI under the name "TY-220®".

The coated iron oxide pigments are for example sold by the company ARNAUD under the names "NANOGARD WCD 2008 (FE 45B FN)®", "NANOGARD WCD 2009® (FE 45B 556®)", "NANOGARD FE 45 BL 345 ®", "NANOGARD FE 45 BL®", or by the company BASF under the name "OXIDE DE FER TRANSPARENT®".

Mention may also be made of mixtures of metal oxides, in particular titanium dioxide and cerium dioxide, including the equal weight mixture of silica-coated titanium dioxide and cerium dioxide, sold by the company IKEDA under the name "SUNVEIL A ®", as well as the mixture of titanium dioxide and zinc dioxide coated with alumina, silica and silicone such as the product "M 261®" sold by the company SACHTLEBEN PIGMENTS or coated with alumina, silica and of glycerin such as the product "M 211®" sold by the company SACHTLEBEN PIGMENTS.

According to the invention, titanium oxide pigments, coated or uncoated, are particularly preferred.

The additional UV screening agents according to the invention may be present in the composition according to the invention at a content ranging from 0.1% to 60% by weight, and in particular from 5% to 30% by weight relative to the total weight of the composition.

Other additives

The composition in accordance with the present invention may also comprise conventional cosmetic adjuvants chosen in particular from organic solvents, ionic or nonionic thickeners, softeners, humectants, opacifiers, stabilizers, emollients, silicones, anti-aging agents. - mousse, perfumes, preservatives, anionic, cationic, non-ionic, zwitterionic or amphoteric surfactants, active ingredients, fillers, polymers, propellants, alkalizing or acidifying agents or any other ingredient usually used in cosmetics and/or dermatological.

Among the organic solvents, mention may be made of short-chain monoalcohols, for example C ₁ -C ₄ , such as ethanol and isopropanol, short-chain C ₂ -C ₈ polyols, such as glycerin, diols such as caprylyl glycol, pentanediol-1,2, propanediol, butanediol, glycols and glycol ethers such as ethylene glycol, propylene glycol, butylene glycol, hexylene glycol, dipropylene glycol or diethylene glycol, 2-ethoxyethanol, diethylene glycol monomethyl ether, triethylene glycol monomethyl ether, sorbitol, and mixtures thereof.

According to a preferred embodiment, it is possible to use more particularly ethanol, propylene glycol, glycerin, and their mixtures.

As thickeners, mention may be made of carboxyvinyl polymers such as Carbopols® (Carbomers) and Pemulen such as Pemulen TR1® and Pemulen TR2® (acrylate/C10-C30-alkylacrylate copolymer); polyacrylamides such as for example the cross-linked copolymers sold under the names Sepigel 305® (CTFA name: polyacrylamide/C ₁₃ - ₁₄ isoparaffin/Laureth 7) or Simulgel 600 (CTFA name: acrylamide/sodium acryloyldimethyltaurate copolymer/isohexadecane/polysorbate 80) by the Seppic; polymers and copolymers of 2-acrylamido 2-methylpropane sulfonic acid, optionally crosslinked and/or neutralized, such as poly(2-acrylamido 2-methylpropane sulfonic acid) marketed by the company Hoechst under the trade name “Hostacerin ^AMPS® ” ( CTFA name: ammonium polyacryloyldimethyl taurate or SIMULGEL 800® sold by the company SEPPIC (CTFA name: sodium polyacryolyldimethyl taurate / polysorbate 80 / sorbitan oleate); copolymers of 2-acrylamido-2-methylpropane sulphonic acid and hydroxyethyl acrylate such as SIMULGEL NS® and SEPINOV EMT 10® marketed by the company SEPPIC; cellulose derivatives such as hydroxyethylcellulose; polysaccharides and in particular gums such as xanthan gum; water-soluble or water-dispersible silicone derivatives such as acrylic silicones, silicones polyethers and cationic silicones and mixtures thereof.

Among the acidifying agents, mention may be made, by way of example, of mineral or organic acids such as hydrochloric acid, orthophosphoric acid, sulfuric acid, carboxylic acids such as acetic acid, tartaric acid, citric acid, lactic acid, sulphonic acids.

Among the basifying agents, mention may be made, by way of example, of aqueous ammonia, alkaline carbonates, alkanolamines such as mono-, di- and triethanolamines as well as their derivatives, sodium or potassium hydroxides.

Preferably, the cosmetic composition comprises one or more basifying agents chosen from alkanolamines, in particular triethanolamine, and sodium hydroxide.

Among the active agents for the care of keratin materials such as the skin, the lips, the scalp, the hair, the eyelashes or the nails, mention may be made, for example, of vitamins and their derivatives or precursors, alone or in mixtures; antioxidants; anti-radical agents; anti-pollutant agents; self-tanning agents; anti-glycation agents; soothing agents; deodorant agents; essential oils ; NO-synthase inhibitors; agents stimulating the synthesis of dermal or epidermal macromolecules and/or preventing their degradation; agents stimulating the proliferation of fibroblasts; agents stimulating the proliferation of keratinocytes; muscle relaxants; cooling agents; tensioning agents; matting agents; depigmenting agents; pro-pigmenting agents; keratolytic agents; desquamating agents; moisturizing agents; anti-inflammatory agents; anti-microbial agents; slimming agents; agents acting on the energy metabolism of cells; insect repellents; substance P or CRGP antagonists; anti-hair loss agents; anti-wrinkle agents; anti-aging agents.

The person skilled in the art will choose the said active ingredient(s) according to the desired effect on the skin, the hair, the eyelashes, the eyebrows, the nails.

Of course, those skilled in the art will take care to choose the optional additional compound(s) mentioned above and/or their quantities in such a way that the advantageous properties inherently attached to the compositions in accordance with the invention are not, or substantially not, altered by the addition(s) envisaged.

DOSAGE FORMS

The compositions in accordance with the invention can be aqueous or anhydrous.

When the compositions are aqueous, they contain at least one aqueous phase.

They can then be in purely aqueous form, that is to say they comprise a quantity of fatty phase of less than 10% by weight, preferably less than 5% by weight, and even more preferably less than 2% by weight relative to the total weight of the composition. Advantageously, the composition in accordance with the invention is essentially aqueous, that is to say it is free of fatty phase.

The compositions according to the invention can also be in the form of an emulsion, simple or complex (O/W, W/O, O/W/O or W/O/W), such as a cream, a milk or of a gel cream.

In the case where the composition in accordance with the invention is aqueous, and it is possible to measure its pH, the latter is generally between 3 and 12 approximately, preferably between 5 and 9 approximately, and even more particularly 5.5 to 8.

The compositions can also be in anhydrous form, such as for example in the form of an oil, a glycolic solution or an alcoholic solution. The term "anhydrous composition" means a composition containing less than 1% by weight of water, or even less than 0.5% of water, and in particular free of water, the water not being added during the preparation of the composition but corresponding to the residual water provided by the mixed ingredients. They may optionally be packaged in an aerosol and come in the form of a foam or a spray.

In the case of compositions in the form of oil-in-water or water-in-oil emulsions, the emulsification processes that can be used are of the paddle or propeller, rotor-stator and HHP type.

To obtain stable emulsions with a low polymer content (oil/polymer ratio >25), it is possible to make the dispersion in the concentrated phase then to dilute the dispersion with the rest of the aqueous phase.

It is also possible, by HHP (between 50 and 800 bars), to obtain stable dispersions with drop sizes down to 100 nm.

The emulsions generally contain at least one emulsifier chosen from amphoteric, anionic, cationic or nonionic emulsifiers, used alone or as a mixture. The emulsifiers are chosen appropriately according to the emulsion to be obtained (W/O or O/W).

As an example of W/O emulsifying surfactants, mention may be made of alkyl esters or ethers of sorbitan, glycerol, polyol, glycerol or sugars; silicone surfactants such as dimethicone copolyols such as the mixture of cyclomethicone and dimethicone copolyol, sold under the name "DC 5225 C®" by the company Dow Corning, and alkyl-dimethicone copolyols such as Laurylmethicone copolyol sold under the name " Dow Corning 5200 Formulation Aid" by the Dow Corning Company; cetyl dimethicone copolyol such as the product sold under the name Abil EM 90R® by the company Goldschmidt and the mixture of cetyl dimethicone copolyol, polyglycerol isostearate (4 moles) and hexyl laurate sold under the name ABIL WE O9 ® by Goldschmidt. One or more co-emulsifiers can also be added thereto, which, advantageously, can be chosen from the group comprising polyol alkyl esters.

Mention may also be made of non-silicone emulsifying surfactants, in particular alkyl esters or ethers of sorbitan, glycerol, polyol or sugars.

As polyol alkyl esters, mention may in particular be made of polyethylene glycol esters such as PEG-30 Dipolyhydroxystearate such as the product marketed under the name Arlacel P135® by the company ICI.

As glycerol and/or sorbitan esters, mention may be made, for example, of polyglycerol isostearate, such as the product marketed under the name Isolan GI 34® by the company Goldschmidt; sorbitan isostearate, such as the product marketed under the name Arlacel 987® by the company ICI; sorbitan isostearate and glycerol, such as the product marketed under the name Arlacel 986® by the company ICI, and mixtures thereof.

For O/W emulsions, mention may be made, for example, as nonionic emulsifying surfactants of polyoxyalkylenated (more particularly polyoxyethylenated and/or polyoxypropylene) fatty acid and glycerol esters; oxyalkylenated sorbitan fatty acid esters; polyoxyalkylenated fatty acid esters (in particular polyoxyethylenated and/or polyoxypropylene) optionally in combination with a fatty acid and glycerol ester, such as the PEG-100 Stearate/Glyceryl Stearate mixture marketed for example by the company ICI under the name Arlacel 165; oxyalkylenated (oxyethylenated and/or oxypropylene) fatty alcohol ethers; sugar esters such as sucrose stearate; fatty alcohol and sugar ethers, in particular alkylpolyglucosides (APG) such as decylglucoside and laurylglucoside marketed for example by the company Henkel under the respective names Plantaren 2000® and Plantaren 1200®, cetostearylglucoside optionally mixed with cetostearyl alcohol, marketed for example under the name Montanov 68® by the company Seppic, under the name Tegocare CG90® by the company Goldschmidt and under the name Emulgade KE3302® by the company Henkel, as well as arachidyl glucoside, for example under the form of the mixture of arachidic and behenic alcohols and of arachidylglucoside marketed under the name Montanov 202® by the company Seppic. According to a particular embodiment of the invention, the mixture of the alkylpolyglucoside as defined above with the corresponding fatty alcohol can be in the form of a self-emulsifying composition, as described for example in document WO- A-92/06778.

When it is an emulsion, the aqueous phase thereof may comprise a nonionic vesicular dispersion prepared according to known methods (Bangham, Standish and Watkins. J. Mol. Biol. 13, 238 (1965), FR 2 315 991 and FR 2 416 008).

The compositions according to the invention find their application in a large number of treatments, in particular cosmetic, of the skin, the lips and the hair, including the scalp, in particular for the protection and/or the care of the skin, the lips and/or the hair, and/or for making up the skin and/or the lips.

Another object of the present invention consists of the use of the compositions according to the invention as defined above for the manufacture of products for the cosmetic treatment of the skin, lips, nails, hair, eyelashes, eyebrows and/or the scalp, in particular care products, sun protection products and make-up products.

The cosmetic compositions according to the invention can for example be used as a make-up product.

Another object of the present invention consists of a non-therapeutic cosmetic process for caring for and/or making up a keratin material, consisting in applying to the surface of said keratin material at least one composition according to the invention as defined above. -above.

Another subject of the invention consists of the use of di-t-butyl pentaerythrityl tetra hydroxycinnamate for photostabilizing a merocyanine of formula (3) as defined above.

Another subject of the invention consists of the use of di-t-butyl pentaerythrityl tetra hydroxycinnamate for photostabilizing a merocyanine of formula (3) as defined above in the presence of one or more dibenzoyl methane derivatives, preferably in the presence of 4-(ter.-butyl)4'-methoxy dibenzoylmethane.

The cosmetic compositions according to the invention can for example be used as care and/or sunscreen products for the face and/or the body of liquid to semi-liquid consistency, such as milks, more or less unctuous creams, gel-creams, pastes. They may optionally be packaged in an aerosol and come in the form of a foam or a spray.

The compositions according to the invention in the form of vaporizable fluid lotions in accordance with the invention are applied to the skin or the hair in the form of fine particles by means of pressurization devices. The devices in accordance with the invention are well known to those skilled in the art and include non-aerosol pumps or “atomizers”, aerosol containers comprising a propellant as well as aerosol pumps using compressed air as propellant. The latter are described in US patents 4,077,441 and US 4,850,517.

The compositions packaged as an aerosol in accordance with the invention generally contain conventional propellants such as, for example, the hydrofluorinated compounds dichlorodifluoromethane, difluoroethane, dimethyl ether, isobutane, n-butane, propane, trichlorofluoromethane. They are preferably present in amounts ranging from 15 to 50% by weight relative to the total weight of the composition.

TOGETHER

According to another aspect, the invention also relates to a cosmetic assembly comprising:
i) a receptacle delimiting one or more compartment(s), said receptacle being closed by a closing element and possibly not being sealed; And
ii) a make-up and/or care composition in accordance with the invention placed inside said compartment(s).

The container can for example be in the form of a pot or a box.

The closure element may be in the form of a lid comprising a mounted cap that can be moved by translation or by pivoting relative to the container housing the said make-up and/or care composition(s).

EXAMPLES

The following examples serve to illustrate the invention without however being limiting.

Example A1: Preparation of Compound (14)
[form 14]

122.23 grams of 3-[(3-methoxypropyl)amino]-2-cyclohexen-1-one are alkylated with dimethyl sulfate or alternatively with diethyl sulfate and treated with 75.45 grams of ethyl cyanoacetate in approximately equimolar proportions in the presence of a base and optionally of a solvent.

The base/solvent combinations shown in the following table are used. Example Base Solvent Example A1.1 DBU (1,8-diazabicyclo[5.4.0]undec-7-ene) dimethylacetamide Example A1.2 Triethylamine isopropanol Example A1.3 3-methoxypropylamine isopropanol Example A1.4 3-methoxypropylamine tert-amyl alcohol Example A1.5 3-methoxypropylamine toluene Example A1.6 3-methoxypropylamine dimethylformamide Example A1.7 3-methoxypropylamine solvent free Example A1.8 N-morpholine isopropanol

The completion of the alkylation reaction can be monitored for example by methods such as TLC, GC or HPLC.

162.30 grams of compound (14) are obtained in the form of a brown oil.

After crystallization, the product is obtained in the form of yellowish crystals.

Melting point: 92.7°C.

Example A2: Preparation of Compound (15)
[form 15]

101.00 grams of 3-[(3-methoxypropyl)amino]-2-cyclohexen-1-one is alkylated with dimethyl sulfate or alternatively with diethyl sulfate and treated with 86.00 grams of 2-cyano-N-(3- methoxy-propyl)-acetamide in approximately equimolar proportions in the presence of a base and optionally of a solvent.

The base/solvent combinations shown in the following table are used.
Example
Base
Solvent Example A2.1 DBU (1,8-diazabicyclo[5.4.0]undec-7-ene) dimethylacetamide Example A2.2 Triethylamine isopropanol Example A2.3 3-methoxypropylamine isopropanol Example A2.4 3-methoxypropylamine tert-amyl alcohol Example A2.5 3-methoxypropylamine toluene Example A2.6 3-methoxypropylamine dimethylformamide Example A2.7 3-methoxypropylamine solvent free

The crude product (15) is obtained as a dark brown oil.

After chromatography on a silica gel column (eluent: toluene/methanol 99/1), 81.8 grams of product are obtained in the form of yellowish crystals.

Melting point: 84.7-85.3°C.

Example A3: Preparation of Compound (27)
[form 27]

13.09 grams of 3-[(3-methoxypropyl)amino]-2-cyclohexen-1-one are alkylated with dimethyl sulfate or alternatively with diethyl sulfate and treated with 10.12 grams of isobutyl cyanoacetate in the presence of a base and optionally a solvent.

The base/solvent combinations shown in the following table are used. Example Base Solvent Example A3.1 DBU (1,8-diazabicyclo[5.4.0]undec-7-ene) dimethylacetamide Example A3.2 Triethylamine isopropanol Example A3.3 3-methoxypropylamine isopropanol Example A3.4 N-methylmorpholine tert-amyl alcohol Example A3.5 3-methoxypropylamine toluene Example A3.6 3-methoxypropylamine dimethylformamide Example A3.7 3-methoxypropylamine solvent free

15.97 grams of crude product (27) are obtained as a dark brown oil.

After chromatography on a silica gel column (eluent: toluene/acetone), 13.46 grams of product are obtained in the form of yellowish crystals.

Melting point: 96.3°C.

Example A4: Preparation of Compound (25)
[form 25]

148.4 grams of 3-[(3-methoxypropyl)amino]-2-cyclohexen-1-one is alkylated with dimethyl sulfate or alternatively with diethyl sulfate and treated with 130.00 grams of 2-ethoxyethyl cyanoacetate in the presence of an organic base and a solvent.

The base/solvent combinations indicated in the table below are used. Example Base Solvent Example A4.1 DBU (1,8-diazabicyclo[5.4.0]undec-7-ene) dimethylacetamide Example A4.2 Triethylamine isopropanol Example A4.3 3-methoxypropylamine isopropanol Example A4.4 N-methylmorpholine tert-amyl alcohol Example A4.5 3-methoxypropylamine toluene Example A4.6 3-methoxypropylamine dimethylformamide Example A4.7 3-methoxypropylamine solvent free

Example of preparation of acrylic polymers:

Molecular weight determination by gel permeation chromatography (GPC):

The sample is prepared by carrying out a solution of the polymer at 10 mg/ml in tetrahydrofuran. The sample is placed in an oven at 54°C for 10 minutes and then in an oscillating shaker for 60 minutes to aid dissolution. After visual inspection, the sample appears completely dissolved in the solvent.

The prepared sample was analyzed using two 300 x 7.5 mm polypore columns (manufactured by Agilent Technologies, a Waters 2695 chromatography system, tetrahydrofuran mobile phase and refractive index detection. The sample was filtered on a filter Nylon 0.45 µm before being injected into the liquid chromatograph The standards used for the calibration are the Easi Vial narrow polystyrene (PS) standards from Agilent Technologies.

Polystyrene standards ranging from 2,520,000 to 162 Daltons were used for calibration.

The system is equipped with a PSS SECcurity 1260 RI detector. The polystyrene calibration curve was used to determine the average molecular weight. The recording of the diagrams and the determination of the various molecular weights was made by the program Win GPC Unichrom 81.

Determination of melting point by differential scanning calorimetry (or DSC):

This method describes the general procedure for determining the melting point of polymers by differential scanning calorimetry. This method is based on ASTM E791 and ASTM D 34182 and DSC calibration is performed according to ASTM E 9672.

Acrylate copolymer behenyl / 2-hydroxyethyl acrylate (Polymer 1):

In a 4-necked flask equipped with a side blade stirrer, internal thermometer, two funnels, a reflux condenser, and an extension for two other necks, 175 g behenyl acrylate, 25 g acrylate of 2 -hydroxyethyl and 0.4 g of 2,2'-azobis(2-methylbutyronitrile (Akzo Nobel) were added for 60 minutes at 80°C in 40 g of isopropanol with stirring after removing oxygen from the system at the using a nitrogen purge for 20 minutes.The mixture was stirred at 80°C for 3 hours.Then the solvent was removed by vacuum distillation,then 1g of dilauryl peroxide was added and the reaction was continued for 60 minutes at 110° C. The step was repeated. The mixture was then cooled to 90° C. and a jet of deionized water was added followed by stirring. The water was removed by vacuum distillation.

Molecular weight: Mn = 7300 g/mol, Mw = 21000, Mw/Mn = 2.8

Melting point: 65°C

Stearyl acrylate / 2-hydroxyethyl acrylate copolymer (Polymer 2):

In a 4-necked flask equipped with a side-blade stirrer, internal thermometer, two funnels, reflux condenser, and extension for two other necks, 155 g stearyl acrylate, 45 g acrylate of 2 -hydroxyethyl and 0.4 g of 2,2'-azobis(2-methylbutyronitrile (Akzo Nobel) were added for 90 minutes at 80°C in 50 g of isopropanol with stirring after removing oxygen from the system at the using a nitrogen purge for 20 minutes.The mixture was stirred at 80°C for 3 hours.Then the solvent was removed by vacuum distillation,then 1g of dilauryl peroxide was added and the reaction was continued for 60 minutes at 125° C. The step was repeated. The mixture was then cooled to 90° C. and a jet of deionized water was added followed by stirring. The water was removed by vacuum distillation.

Molecular weight: Mn = 7500 g/mol, Mw = 19000, Mw/Mn = 2.6

Melting point: 49°C

Examples of formulations

Comparative Examples 1 and 2

Compositions 1 and 2 are prepared from the ingredients indicated in the table below, the amounts of which are expressed as % by weight of raw material (MP) relative to the total weight of the composition. Phase Ingredients Composition 1 (Excluding invention) Composition 2 (Invention) A1 WATER QSP 100 QSP 100 A1 Conservatives QS QS A1 TRISODIUM ETHYLENEDIAMINE DISUCCINATE 0.3 0.3 A1 PEG-8 4 4 A1 DIPROPYLENE GLYCOL 4 4 A1 ACRYLATES COPOLYMER
Carbopol Aqua SF1 by Lubrizol 2 2 A2 TRIETHANOLAMINE QS pH 6.7 QS pH 6.7 A3 TEREPHTHALYLIDENE DICAMPHOR SULFONIC ACID
Mexoryl SX by Noveal 1 1 B BUTYL METHOXYDIBENZOYLMETHANE
Parsol 1789 from DSM Nutritional products 2 2 B PENTAERYTHRITYL TETRA-DI-T-BUTYL HYDROXYHYDROCINNAMATE
BASF Tinogard TT - 0.1 B ETHYLHEXYL SALICYLATE
Symrise Neo Heliopan OS 5 5 B ETHYLHEXYL TRIAZONE
Uvinul T150 from BASF 5 5 B DROMETRIZOLE TRISILOXANE
Mexoryl XL from Noveal 2 2 B DIETHYLAMINO HYDROXYBENZOYL HEXYL BENZOATE
Uvinul A+ from BASF 1 1 B BIS-ETHYLHEXYLOXYPHENOL METHOXYPHENYL TRIAZINE
BASF Tinosorb S 4.5 4.5 B DIISOPROPYL SEBACATE
Dub Dis by Sterinerie Dubois 8 8 B DIISOPROPYL ADIPATE
Dub Dipa by Stearine Dubois 4 4 B C12-22 ALKYL ACRYLATE/HYDROXYETHYLACRYLATE COPOLYMER
(polymer 1 synthesized previously) 2.5 2.5 B Compound 25 1 1 VS ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER
Lubrizol Pemulen TR1 0.15 0.15 VS SODIUM POLYACRYLATE
BASF Cosmedia SP 0.2 0.2 D WATER 10 10 E SILICA 1 1 E ALUMINUM STARCH OCTENYLSUCCINATE 2 2 F ALCOHOL DENAT. 5 5

Method of preparation of the compositions:

Phase A1 is prepared by mixing all the ingredients, then phase A2 is added for neutralization and formation of the gel. This is followed by the addition of phase A3. All of this preparation of phase, which will be called A in the following, is carried out by heating to 65°C and stirring with blades (50 revolutions/min).

Phase B is prepared by mixing all the ingredients by heating to 80°C with magnetic stirring until a clear and homogeneous phase is obtained.

The emulsification is carried out by dispersing phase B in phase A at 65° C. and with vigorous stirring (blades at 80 revolutions/min and turbine at 11,000 revolutions/min) for 5 minutes. An oil-in-water emulsion is obtained. The temperature of the mixture is then gradually reduced to return to ambient temperature while maintaining the same agitation until the end. Around 55°C, phase C thickeners are added (5 minutes), then phase D (5 minutes) and phase E fillers from 35°C. Finally, the alcohol of phase E is added once the mixture has returned to room temperature.

Results :

Once prepared, compositions 1 and 2 are each spread on 6 Europlast brand PMMA plates at a rate of 2.0 to 2.1 mg/cm² (which corresponds to between 16 and 17 mg over 8 cm²). 3 of the 6 plates are then exposed under a Suntest (HERAEUS) with a UV dose of 43.2 J/cm² at a temperature of 40° C. while the others are kept at the same temperature in the dark.

After irradiation, the residual contents of 2-ethoxyethyl 2-cyano{3-[(3-methoxypropyl)amino]-cyclohex-2-en-1-ylidene}ethanoate in each of the 6 plates are measured by standard chromatography methods. HPLC.

The residual fraction after irradiation expressed in % corresponds to the ratio of the average of the residual contents of the ingredient contained on the 3 plates having been exposed compared to the average of the residual contents of the 3 plates not having been exposed for the same composition .

The results obtained are collated in the table below. Residual fraction
after irradiation Membership 1
(Excluding invention) Membership 2
(Invention) 2-Ethoxyethyl 2-cyano{3-[(3-methoxypropyl)-amino]cyclohex-2-en-1-ylidene}-ethanoate
(compound 25) 69%±0.8% 76% ± 0.5%

These results show that composition 2 according to the invention has a residual fraction of merocyanine compound substantially higher than that of comparative composition 1, which shows that in the presence of di-t-butyl pentaerythrityl tetra hydroxycinnamate, the merocyanine compound has better photostability against UV radiation.

Claims (18)

Cosmetic or dermatological composition comprising:
a) at least one merocyanine corresponding to the following formula (3), as well as their isomeric geometric forms, in particular E/E or E/Z:
[Formula 3]

in which :
A is –O- or –NH;
R is a C ₁ -C ₂₂ alkyl group, a C ₂ -C ₂₂ alkenyl group, a C ₂ -C ₂₂ alkinyl group, a C ₃ -C ₂₂ cycloalkyl group or a C ₃ -C ₂₂ cycloalkenyl group, said groups possibly being interrupted by one or more O; And
b) di-t-butyl pentaerythrityl tetra hydroxycinnamate. Composition according to Claim 1, in which the merocyanines of formula (3) are chosen from the following compounds, as well as their isomeric geometric forms, in particular E/E or E/Z: 14
ethyl (2Z)-cyano{3-[(3-methoxypropyl)amino]cyclohex-2-en-1-ylidene}ethanoate 15
(2Z)-2-cyano-N-(3-methoxypropyl)-2-{3-[(3-methoxypropyl)amino]cyclohex-2-en-1-ylidene}ethanamide 25
2-ethoxyethyl (2Z)-cyano{3-[(3-methoxypropyl)amino]cyclohex-2-en-1-ylidene}ethanoate 27
2-methylpropyl (2Z)-cyano{3-[(3-methoxypropyl)amino]cyclohex-2-en-1-ylidene}ethanoate 29

2-butoxyethyl (2Z)-cyano{3-[(3-methoxypropyl)amino]cyclohex-2-en-1-ylidene}ethanoate 31

3-methoxypropyl (2Z)-cyano{3-[(3-methoxypropyl)amino]cyclohex-2-en-1-ylidene}ethanoate
37
3-ethoxypropyl (2Z)-cyano{3-[(3-methoxypropyl)amino]cyclohex-2-en-1-ylidene}ethanoate Composition according to either of Claims 1 and 2, in which the merocyanine of formula (3) is 2-ethoxyethyl (2Z)-cyano{3-[(3-methoxypropyl)amino]cyclohex-2-en-1-ylidene }ethanoate (25) in its E/Z geometric configuration with the following structure:
[form 25]

and/or in its geometric configuration E/E with the following structure:
[form 25bis]
Composition according to any one of Claims 1 to 3, in which the di-t-butyl pentaerythrityl tetrahydroxycinnamate is present in a content ranging from 0.01% to 2.5% by weight, preferably from 0.05% to 1.5% by weight, more preferably from 0.1% to 0.3% by weight relative to the total weight of the composition. Composition according to any one of Claims 1 to 4, comprising at least one polymer comprising monomeric units of formulas (A) and (B):
[form A] [form B]

in which :
R1, independently of one another, is chosen from alkyl or alkylene radicals, and
at least 60% by weight of the R1 groups are radicals chosen from stearyl and behenyl radicals, the percentage by weight relating to the sum of all the R1 groups present in the polymer, and
the weight ratio of the sum of all the hydroxyethyl acrylate units to the sum of all the acrylate units carrying the group R1 ranges from 1:30 to 1:1;
and the sum of the total of units A and B is at least 95% by weight of the total weight of the polymer,
the polymer having a number average molecular weight Mn ranging from 2000 to 9000 g/mol. Composition according to Claim 5, in which the additional polymer R1 consists of an alkyl radical, preferably of a C16-C22 alkyl radical, and more preferably of a behenyl or stearyl radical. Composition according to either of Claims 5 and 6, in which in the additional polymer at least 70% by weight of the R1 groups are behenyl or stearyl radicals, preferably at least 80% by weight, more preferably at least 90% by weight . Composition according to any one of Claims 5 to 7, in which in the additional polymer all the R1 groups are stearyl or behenyl radicals. Composition according to any one of Claims 5 to 8, in which, in the additional polymer, the said weight ratio ranges from 1:15 to 1:1, preferably ranges from 1:10 to 1:4. Composition according to any one of Claims 5 to 9, in which the additional polymer has a number-average molecular weight Mn ranging from 5000 to 9000 g/mol. Composition according to any one of Claims 5 to 10, in which the additional polymer has a melting point ranging from 40°C to 70°C, and preferably ranging from 45°C to 67°C. Composition according to any one of Claims 5 to 11, in which in the additional polymer at least 60% by weight of the R1 groups are stearyl radicals, and the said additional polymer has a melting point ranging from 40 to 60°C, and preferably ranging from 45 to 55°C. Composition according to any one of Claims 5 to 12, in which in the additional polymer at least 60% by weight of the R1 groups are behenyl radicals, and the said additional polymer has a melting point ranging from 60°C to 70°C, and preferably ranging from 63°C to 67°C. Composition according to any one of claims 1 to 13 further comprising one or more additional UV screening agents, preferably
one or more compounds derived from dibenzoylmethane chosen from those of the following formula, and/or mixtures thereof:
[form 6]

in which :
R ₁ , R ₄ , R ₅ and R ₆ represent, independently of each other, a hydrogen atom; a hydroxy radical; an alkyl radical, linear or branched, C ₁ -C ₄ ; or a C ₁ -C ₄ alkoxy radical, linear or branched; And
R ₂ and R ₃ represent, independently of each other, a hydrogen atom; a hydroxy radical; an alkyl radical, linear or branched, C ₁ -C ₄ ; a C ₁ -C ₄ alkoxy radical, linear or branched; or form with the 2 carbon atoms of the covalent bonds CR ₂ and CR ₃ a 5- or 6-membered heterocycle optionally substituted by a hydrocarbon chain, linear or branched, C ₁ -C ₄ . Composition according to Claim 14, in which the dibenzoylmethane derivative(s) are chosen from 2-methyldibenzoylmethane, 4-methyldibenzoylmethane, 4-isopropyldibenzoylmethane, 4-tert-butyldibenzoylmethane, 2,4-dimethyldibenzoylmethane, 2,5- dimethyldibenzoylmethane, 4,4'-diisopropyldibenzoylmethane, 4,4'-dimethoxydibenzoylmethane, 4-tert-butyl-4'-methoxydibenzoyl-methane, 2-methyl-5-isopropyl-4'-methoxydibenzoylmethane, 2-methyl -5-tert-butyl-4'-methoxydi-benzoylmethane, 2,4-dimethyl-4'-methoxydibenzoylmethane, 2,6-dimethyl-4-tert-butyl-4'-methoxy-dibenzoylmethane, 1-( 4-tert-Butylphenyl)-3-(2-hydroxyphenyl)-propane-1,3-dione, 1-(4-methoxy-1-benzofuran-5-yl)-3-phenyl-propane-1,3- dione; preferably chosen, alone or as a mixture, from 4-tert-butyl-4'-methoxydibenzoylmethane and/or 4-isopropyldibenzoylmethane; preferably chosen from 4-tert-butyl-4'-methoxydibenzoylmethane. Composition according to any one of claims 1 to 15 comprising 4-tert-butyl-4'-methoxydibenzoylmethane. Non-therapeutic cosmetic process for caring for and/or making up a keratin material comprising the application to the surface of the said keratin material of at least one composition as defined in any one of Claims 1 to 16. Use of di-t-butyl pentaerythrityl tetra hydroxycinnamate for photostabilizing a merocyanine as defined in any one of claims 1 to 3.