FR3130131A1 - DISPERSION COMPRISING A POLYMERIC PARTICLE, A STABILIZING AGENT WITH A CYCLOALKYL GROUP, AN OIL, AND A POLYOL, PROCESS FOR THE TREATMENT OF KERATIN MATERIALS USING THE DISPERSION - Google Patents

Abstract

Title: DISPERSION COMPRISING A POLYMERIC PARTICLE, A STABILIZING AGENT WITH A CYCLOALKYL GROUP, AN OIL, AND A POLYOL, PROCESS FOR THE TREATMENT OF KERATIN MATERIALS IMPLEMENTING THE DISPERSION The present invention relates to a dispersion (A) comprising at least two particles i) consisting of polymer of ethylenic monomers, ii) at least one stabilizing agent comprising at least one (C3-C12)cycloalkyl group, iii) at least one hydrocarbon fatty substance which is liquid at 20°C and 1 atmosphere, iv) at least one polyol liquid at 20°C and 1 atmosphere and optionally v) water. The invention also relates to a process for treating keratin materials, in particular human materials such as the skin, the eyelashes, the eyebrows, implementing the application to said materials of at least one dispersion (A); a process for preparing the dispersion (A), the process for preparing the dispersion (A), the polymeric material (C). The dispersion (A), and the process for treating keratin materials as defined above, make it possible in particular to obtain a treatment of said materials, a filling of irregularities such as wrinkles or fine lines in the skin.

Description

DISPERSION COMPRISING A POLYMERIC PARTICLE, A STABILIZING AGENT WITH A CYCLOALKYL GROUP, AN OIL, AND A POLYOL, PROCESS FOR THE TREATMENT OF KERATIN MATERIALS USING THE DISPERSION

The present invention relates to a dispersion (A) comprising at least two particles i) consisting of polymer of ethylenic monomers, ii) at least one stabilizing agent comprising at least one (C ₃ -C ₁₂ )cycloalkyl group, iii) at least one hydrocarbon fatty liquid at 20°C and 1 atmosphere, iv) at least one polyol liquid at 20°C and 1 atmosphere and optionally v) water. A subject of the invention is also a method for treating keratin materials, in particular human materials such as the skin, the eyelashes, the eyebrows, implementing the application to said materials of at least one dispersion (A); a process for preparing the dispersion (A), the process for preparing the dispersion (A), the polymeric material (C).

During the aging process, different signs appear on the skin, very characteristic of this aging, resulting in particular in a modification of the structure and functions of the skin. The main clinical signs of skin aging are in particular the appearance of fine lines and/or deep wrinkles, which increase with age.

It is known to treat these signs of aging by using anti-aging cosmetic compositions containing one or more anti-aging active agents. However, these active agents have the drawback of only being effective for the treatment of wrinkles and/or fine lines after repeated applications. However, it is increasingly sought to obtain an immediate effect from the active agents used, leading rapidly to a smoothing of wrinkles and fine lines and/or to the disappearance of signs of fatigue.

It can also be sought to mask skin imperfections perceived as unsightly. By way of illustration of these imperfections, mention may in particular be made of skin irregularities linked to helioderma, acne scars, spots or signs of aging such as wrinkles, fine lines, dilated pores and hyperkeratinization. The masking of these expected skin imperfections can be a masking of surface irregularities by making the appearance of the skin smoother and more homogeneous.

Cosmetic products often require the use of a film-forming polymer to obtain a deposit of the product on keratin materials with good cosmetic properties. In particular, it is necessary for the film-forming deposit to have good hold, in particular for the deposit not to transfer on contact with fingers, clothing, as well as good hold in contact with water, in particular rain. or during the shower or even that the deposit is insensitive to perspiration or to sebum, as well as to the fatty substances of food, in particular food fatty substances such as oils.

It is known to use dispersions of polymer particles in organic media such as hydrocarbon oils. The polymers are used in particular as a film-forming agent in make-up products such as mascaras, eyeliners, eye shadows or lipsticks. Document EP 0 749 747 describes in the examples dispersions in hydrocarbon oils (paraffin oil, isododecane) of acrylic polymers stabilized with polystyrene/copoly(ethylene-propylene) diblock copolymers. The film obtained after application of the dispersion to the skin is not very shiny. Document FR 1 362 795 also describes the use of a dispersion of surface-stabilized polymer particles containing hydrocarbon oils for making up the lips and eyelashes. Document WO 2010/046229 describes dispersions in isododecane of stabilized acrylic polymers. Document FR 1 362 795 describes the use of a dispersion of surface-stabilized polymer particles containing hydrocarbon oils for making up the lips and eyelashes.

In the field of dyeing keratin materials, it is known to dye keratin fibers by different techniques using direct dyes for non-permanent dyes or dye precursors for permanent dyes, or by pigments in particular when they are It is about making up keratin fibers such as eyelashes and eyebrows. However, the hold of dyes and pigments, particularly against external aggressions, water, sebum and oils, is not always satisfactory over time.

For example, document FR 3 029 786 is concerned with dispersions for making up polymer particles stabilized by at least one stabilizing agent which is a C ₈ alkyl (meth)acrylate homopolymer or a copolymer of (meth) C ₈ alkyl (2-ethylhexyl) acrylate and C ₁ -C ₄ alkyl (meth)acrylate. These dispersions are not always satisfactory in terms of resistance to fatty substances, to sebum, which can be a hindrance to their use in making up the lips, for example. In addition, these dispersions may have a feel that is considered too “sticky” after application to keratin materials and that may be prohibitive for certain applications such as making up the lips or the eyelashes.

It is therefore advantageous to provide a process for treating keratin materials such as the skin which is easy to apply, which can mask imperfections of said skin, fill in wrinkles and/or fine lines, and even mask scars, by application of a composition optionally comprising one or more cosmetic active agents such as UV filters or anti-aging active agents such as anti-wrinkle agents, without having to require injections into the dermis or epidermis (for example with collagen or hyaluronic acid). It would also be of interest for the cosmetic composition to be stable for obvious storage reasons.

In addition, users are demanding aqueous galenics, containing as few volatile compounds as possible. Environmental issues also lead to reducing the use of volatile compounds as much as possible. Thus, one of the aims of the present invention is to provide a composition with a reduced content of volatile compounds. Another object is to provide a film-forming composition containing an aqueous phase opening the way to a wider formulation field. It is also desired to put as little surfactant as possible, or even not to put any, in the cosmetic composition for reasons related to the environment but also to avoid in the long run potentially altering the keratin materials. It is therefore increasingly sought after by users of cosmetic compositions with little or no surfactant in products intended to be applied to keratin materials.

Also, it would be of interest to provide an emulsifying composition, which is capable of forming a stable emulsion in the presence of water of the hydrogel type with a very small amount (<5% by weight relative to the total weight of the composition ) even in the absence of surfactant, in particular nonionic and/or ethoxylated, which are of petrochemical origin.

A hydrogel is a gel in which the swelling agent is mostly water. The matrix of a hydrogel is generally a network of polymers which are insoluble in water and capable of swelling substantially in the presence of a large quantity of water or of aqueous composition. Hydrogels based on polymers of the poly(acrylic acid) polymer type are used, for example, in beauty masks with the aim of moisturizing the skin, restoring its elasticity or as anti-aging ( Journal of Materials Science: Materials in Medicine , S. Mitura et al 31:50, pp. 1-14 (2020), https://doi.org/10.1007/s10856-020-06390-w). For beauty masks, sticky hydrogels in the presence of crosslinkers are used in particular (see for example WO 2014/077519 A1, FR 2 924 615). Acrylate-based hydrogels, on the other hand, are widely applied in personal care products to absorb fluids as they can to keep moisture away from the skin, promoting skin health, preventing diaper rash and provide comfort ( Journal of Materials Science: Materials in Medicine , S. Mitura et al. 31:50 (2020)).

Another object of the present invention is to provide a composition for treating keratin materials, in particular the skin, preferably human skin, and more preferably the skin of the face, adhesive and if possible non-sticky, exhibiting good resistance to - resists external aggressions, and over time, does not disgorge, resistant to sweat, sebum, insensitive to oils such as edible oils. In addition, the composition may comprise cosmetic active agents such as those for obtaining a tightening effect on the skin, body, face and hair care, Ultra-Violet (UV) protection, face make-up, lips, and eyelashes, eyebrows, and hair. Said composition may be intended in particular for caring for and/or making up, in particular for the face and/or the neck.

It is also sought to obtain polymeric materials which, once applied to the substrate, have properties of elastic, flexible, comfortable mechanical resistance, which do not generate discomfort on application or over time, such as sensations of tightness, dryness, and which can conform to the surface, or even fill in the irregularities or imperfections of the surface of the substrate such as wrinkles, fine lines, scars, etc. and which is not sticky. It would also be interesting if said materials could be sufficiently affine with the substrate so that they do not detach from the substrate easily and that they could nevertheless, if sufficient force is exerted with the hand, be removed for example with a fingernail. , without it being painful. It is very difficult to find materials that have this good substrate adhesion/support withdrawal compromise, especially when the support is flexible and has imperfections such as skin.

These technical problems have been solved by the use of a dispersion (A) in particular in the form of a hydrogel, for the treatment of keratin materials, in particular α) keratin fibers in particular human such as the eyelashes, and eyebrows or β ) human skin, in particular of the face, in which the dispersion (A) comprises:
i) at least two particle(s) of different chemical structures consisting of polymer(s) obtained by polymerization of monomers chosen from ethylenic monomers of:
a ₁ ) (C ₁ -C ₄ )(alkyl)acrylate of (C ₁ -C ₄ )alkyl whose (C ₁ -C ₄ )alkyl group(s) are optionally substituted by one or more group(s) chosen from hydroxy , and (di)(C ₁ -C ₄ )(alkyl)amino ,
a ₂ ) poly[oxy(C ₁ -C ₄ )alkylene] (C ₁ -C ₄ )(alkyl)acrylate,
a ₃ ) ethylenic monomers comprising one or more groups chosen from carboxy, anhydride, phosphoric acid, and sulphonic acid;
it being understood that each particle results from the polymerization of one or more ethylenic monomer(s) a ₃ ); And
ii) one or more polymeric stabilizing agent(s) chosen from:
d) ethylenic polymers of monomers of (C ₁ -C ₆ )(alkyl)acrylate of (C ₃ -C ₁₂ )cycloalkyl, preferably ethylenic homopolymers of (C ₁ -C ₆ )(alkyl)acrylate of (C ₃ -C ₁₂ )cycloalkyl, more preferentially the ethylenic homopolymers of (meth)acrylate of (C ₃ -C ₁₂ )cycloalkyl; And
e) copolymers of ethylenic monomers of:
e ₁ ) (C ₁ -C ₆ )(alkyl)acrylate (C ₃ -C ₁₂ )cycloalkyl, and
e ₂ ) (C ₁ -C ₄ )(alkyl)acrylate of (C ₁ -C ₄ )alkyl, preferably the copolymers of (meth)acrylate of (C ₃ -C ₁₂ )cycloalkyl and (meth)acrylate of (C ₁ -C ₄ )alkyl; And
iii) one or more liquid fat(s) at 20°C and 1 atmosphere, preferably volatile hydrocarbon(s); And
iv) one or more polyol(s) liquid(s) at 20°C and 1 atmosphere; And
v) optionally water; And
vi) optionally one or more cosmetic active ingredient(s) different from iii) and from iv), chosen from f) dyes, g) pigments; h) active ingredients for caring for keratin materials, in particular the skin, in particular antioxidants and moisturizers other than iv), i) UV filters (A) and/or (B), or j) mixtures of f) to i).

More particularly, the subject of the invention relates to the use of the dispersion (A) as defined above for the treatment of keratin materials, in particular α) keratin fibers, in particular human fibers such as the hair, eyelashes, eyebrows, and/ or the shaping of keratin fibers such as hair, or for the treatment of β) human skin, in particular of the face, preferably for filling in skin imperfections such as wrinkles and fine lines or scars while making up said keratin materials, or for filling in skin imperfections such as wrinkles and fine lines or scars while providing care for said keratin materials, such as moisturizing the skin.

A subject of the invention is also the dispersion (A) as defined previously, as well as a process for treating keratin materials, preferably α) keratin fibers, in particular human fibers such as the hair, the eyelashes, eyebrows or β) the human skin, in particular of the face, for filling in skin imperfections such as wrinkles and fine lines or scars, comprising the application to said materials of a dispersion (A), as defined previously.

The invention also relates to a method for preparing the dispersion (A) as defined previously, and after evaporation of the water v) if present in the medium and of the fatty substances iii), the polymeric material (C) obtained by said process.

A subject of the invention is also a kit or device comprising several compartments comprising the ingredients i) to iv), optionally v) and vi) as defined previously.

A subject of the invention is also a composition, preferably cosmetic, comprising the dispersion (A) as defined previously, the process for applying said composition to keratin materials.

A subject of the invention is also a process for treating keratin materials, preferably α) keratin fibres, in particular human ones, such as the hair, eyelashes, eyebrows or β) human skin, in particular of the face, in particular of the lips, comprising the application to said materials of at least one dispersion (A), as defined previously.

A subject of the invention is also the use of a dispersion (A) as defined above for the treatment of keratin materials, in particular α) keratin fibers, in particular human fibers such as eyelashes, eyebrows or β) human skin in particular of the lips, comprising the application to said materials of at least one dispersion (A), for filling in skin imperfections such as wrinkles and fine lines or scars, for skin care and/or for making up the skin.

The dispersions (A) of the invention, in particular the hydrogels, are stable. Furthermore, after application of the dispersions (A) to the keratin materials, the material obtained (C) is film-forming, adheres to said materials. In addition, active ingredients such as pigments are not altered in terms of color when filling in imperfections, wrinkles, fine lines or scars.

Thus the dispersion (A) according to the invention is applied to the skin with the aim of obtaining an effect of filling in the imperfections of the keratinous materials, in particular of the skin of the face, and the polymeric material (C) which results from the application of the dispersion (A) to said materials after evaporation of the fatty substance(s) iii) and of the water v) if present, is film-forming and adhesive to the said keratin materials. Mention may in particular be made of applications in the field of make-up (lipstick, mascara, filling in wrinkles, fine lines, and masking of imperfections).

The dispersion (A), and the process for treating keratin materials as defined above, make it possible to obtain a treatment of said materials that is resistant in particular to shampoos, sebum, sweat, and/or water, but also to fatty substances in particular food such as oils. In addition, the dispersion is easy to implement in compositions, in particular cosmetic compositions, is easy to manufacture and remains stable over time. Indeed, the dispersion (A) in accordance with the present invention makes it possible to obtain deposits of polymeric materials (C) on said keratinous materials (substrate) which are highly resistant to external aggressions, in particular to sebum and fatty substances which are found in food, in particular liquid fatty substances such as vegetable oils and in particular olive oil. It appears that the make-up produced with at least one dispersion (A), in particular lip make-up, is particularly resistant to external attacks such as liquid fatty substances, in particular vs. vegetable oils such as olive oil. In addition, the makeups obtained with the dispersions (A) are very aesthetic. These dispersions of polymer particles are found at a high dry matter content in the hydrocarbon-based liquid fatty substance(s) iii), which makes them easy to formulate.

Furthermore, the polymeric materials (C) of the invention obtained after application to the substrate and evaporation of the solvents [water v) and/or fatty substances iii)] of the dispersion (A) are flexible and conform to the surface, significantly reduce or even fill in the surface irregularities and imperfections of said substrate, in particular flexible, in particular the skin, such as filling in wrinkles, fine lines, scars and other skin imperfections. The polymeric materials of the invention have a good affinity with the substrate, do not detach from the substrate easily but sufficiently so that they can be removed, if necessary.

Within the meaning of the present invention, and unless a different indication is given:
- A "alkyl radicalis a saturated hydrocarbon group at C₁-VS₈, linear or branched, especially in C₁-VS_6,preferably in C₁-VS₄such as methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl and t-butyl;
- a stem "( VS ₉ -VS ₂₂ )alkylis a saturated hydrocarbon group at C₉-VS₂₂, especially in C₁₀-VS_{20 ,}preferentially in VS₁₂-VS₁₈, more preferably in VS₁₂-VS_{16 ,}linear or branched, preferably linear, such as lauryl (C₁₂), myristyl (C₁₄), hexadecyl (C₁₆), stearyl (C₁₈), arachidyl (C₂₀), behenyl (C₂₂); more specifically(VS ₉ -VS ₁₈ )alkyl isa saturated hydrocarbon group at C₉-VS₁₈linear or branched preferably linear;
- A "radical alkyleneis a divalent saturated hydrocarbon group at C₁-VS₈, linear or branched, especially in C₁-VS_6,preferably in C₁-VS₄such as methylene, ethylene, or propylene;
- by "(di)(C ₁ -VS ₄ )(alkyl)amino» means an amino radical -NH₂; a radical (C₁-VS₄)alkylamino such as methylamino ethylamino; a radical di(C₁-VS₄) alkylamino such as dimethylamino, diethylamino preferably dimethylamino;
- a stem "cycloalkyl» is a saturated cyclic hydrocarbon group comprising from 1 to 3 rings, preferably 2 rings, and comprising from 3 to 12 carbon atoms, preferably between 5 and 10 carbon atoms, such as cyclopentyl, cyclohexyl, cycloheptyl, norbornyl, or isobornyle the cycloalkyl radical being able to be substituted by one or more groups (C₁-VS₄)alkyl such as methyl, preferably the cycloalkyl radical is an isobornyl group.
- a stem "cyclic» is a cyclic hydrocarbon group, saturated or unsaturated, aromatic or non-aromatic, comprising from 1 to 3 rings, preferably 1 ring, and comprising from 3 to 10 carbon atoms such as cyclohexyl or phenyl;
- a stem "aryl» is an aromatic unsaturated cyclic radical, comprising from 6 to 12 carbon atoms, mono or bicyclic, fused or not, preferably the aryl group comprises 1 ring and 6 carbon atoms such as phenyl;
- a stem "aryloxy» is an aryl-oxy radicaliearyl-O- with aryl as previously defined, preferably phenoxy;
- a stem "aryl (VS ₁ -VS ₄ ) there vs oxyis an aryl-(C₁-VS₄)alkyl-O-, preferably benzoxy;
- by "materials keratinous» is particularly meant the skin (keratinized epithelium) and the human keratin fibers such as the hair, the eyelashes, eyebrows, and body hair, preferentially the hair, the eyebrows and the eyelashes, even more preferentially the eyelashes and eyebrows;
- by monomer “soluble“, is meant in the present description any monomer whose polymer, in particular the homopolymer, is soluble, at 5% by weight, at 20° C., and at atmospheric pressure in the liquid hydrocarbon medium consisting of liquid hydrocarbon fatty substance(s) ( s) iii) dispersal. The polymer, in particular the homopolymer, is completely dissolved in the liquid carbonaceous medium, visually at 20°C i.e. there is no visual note of deposit, nor precipitate, nor agglomerate, nor insoluble sediment;
- by monomer “insoluble", means any monomer whose polymer, in particular the homopolymer, is not in soluble form, that is to say completely dissolved at a concentration greater than 5% by weight at room temperature (20 ° C) in said medium liquid hydrocarbon consisting of iii) liquid hydrocarbon fatty substance(s). However, the so-called insoluble monomers can, as monomers, be soluble in the liquid hydrocarbon medium consisting of liquid hydrocarbon fatty substance(s) iii) of the dispersion, it being understood that they become insoluble after polymerization.
- by "homopolymer of ethylenic monomers“means a polymer resulting from the polymerization of identical monomers;
- by "copolymer of ethylenic monomers“means a polymer resulting from the polymerization of different monomers, in particular at least 2 different monomers. Preferably, the ethylenic copolymer of the invention is derived from 2 or 3 different monomers, more preferably derived from 2 different monomers;
- by "ethylenic monomer» means an organic compound comprising one or more unsaturations of the >C=C< types, conjugated or not, capable of polymerizing;
- by "ethylenic polymer“means a copolymer of ethylenic monomers or a homopolymer of ethylenic monomers;
- by "(meth)acrylate", respectively "(meth)acrylic», means acrylate or methacrylate, respectively acrylic or methacrylic;
- by "particle(s) of different chemical structure» particles in which at least one of the monomers constituting them is different and/or in which the monomers constituting them are identical and the proportions of the monomers are different; a copolymer and a homopolymer thus constitute particles of different chemical structure; a copolymer of x% of monomer X and y% of monomer Y is different from a copolymer of z% of monomer X and t% of monomer Y if z is different from x and t is different from y; within the meaning of the present invention, "particle(s) of different chemical structure" And "particle(s) of different chemical compositionare equivalent;
- by" fat bodyis meant an organic compound that is immiscible in water at ordinary room temperature (25°C) and at atmospheric pressure (760 mm Hg) (solubility less than 5% and preferably 1% even more preferably at 0.1%). They have in their structure at least one hydrocarbon chain comprising at least 6 carbon atoms or a sequence of at least two siloxane groups. In addition, fatty substances are generally soluble in organic solvents under the same temperature and pressure conditions, such as, for example, ethanol, ether, petroleum jelly or decamethyl cyclopentasiloxane. These fatty substances are neither polyoxyethylenated nor polyglycerolated. They are different from fatty acids because salified fatty acids constitute soaps that are generally soluble in aqueous media;
- by fat body "liquidis meant in particular a fatty substance that is liquid at 25° C. and 1 atmosphere, preferably said fatty substance has a viscosity less than or equal to 7000 centipoise at 20° C.;
- by fat body "hydrocarbon» means a fatty substance which comprises at least 50% by weight, in particular from 50 to 100% by weight, for example from 60 to 99% by weight, or even from 65 to 95% by weight, or even from 70 to 90% by weight, relative to the total weight of said fatty substance, of carbon compound, having an overall solubility parameter according to HANSEN's solubility space of less than or equal to 20 (MPa)1/2, or of a mixture of such compounds ;
- The global solubility parameter δ according to the HANSEN solubility space is defined in the article "Solubility parameter values" by Grulke, in the work "Polymer Handbook" 3^thedition, Chapter VII, pages 519-559 by the relation δ = ( d_D ²+d_P ²+d_H ²)^1/2in which: - d_Dcharacterizes the LONDON dispersion forces resulting from the formation of dipoles induced during molecular shocks, - d_Pcharacterizes the DEBYE interaction forces between permanent dipoles, - d_Hcharacterizes the specific interaction forces (type hydrogen bonds, acid/base, donor/acceptor, etc.); The definition of solvents in the three-dimensional solubility space according to HANSEN is described in the article by HANSEN: "The three dimensional solubility parameters" J. Paint Technol. 39, 105 (1967);
- by "oil» means a fatty substance that is liquid at room temperature at room temperature (25°C) and atmospheric pressure;
- by "hydrocarbon oilmeans an oil formed essentially, or even consisting, of carbon and hydrogen atoms, and possibly of oxygen and nitrogen atoms, and not containing any silicon or fluorine atoms. It may contain hydroxy, ester, ether, carboxylic acid, amine and/or amide groups;
- by "volatile oilmeans an oil (or non-aqueous medium) capable of evaporating on contact with keratin materials, in particular the skin, in less than an hour, at ambient temperature and atmospheric pressure. The volatile oil is a volatile cosmetic oil, liquid at ambient temperature, having in particular a non-zero vapor pressure, at ambient temperature and at atmospheric pressure, in particular, having a vapor pressure ranging from 0.13 Pa to 40,000 Pa (10^-3to 300 mm Hg), and preferably ranging from 1.3 Pa to 13,000 Pa (0.01 to 100 mm Hg), and preferably ranging from 1.3 Pa to 1300 Pa (0.01 to 10 mm Hg) ;
- by "non-volatile oil“, means an oil having a vapor pressure of less than 0.13 Pa at room temperature and atmospheric pressure;
- by "silicone oil“means an oil comprising at least one silicon atom, and in particular at least one Si—O group. Silicone oil can be volatile or non-volatile;
- by "dispersing agentis meant a compound which makes it possible to protect the dispersed particles against their agglomeration or flocculation. This dispersing agent can be a surfactant, an oligomer, a polymer or a mixture of several of them, bearing one or more functionalities having a strong affinity for the surface of the particles to be dispersed; in particular, they can cling physically or chemically to the surface of the pigments. These dispersing agents also have at least one functional group that is compatible or soluble in the continuous medium. Said agent can be charged, it can be anionic, cationic, zwitterionic or neutral;
- by "pigment", we mean all the pigments bringing color to keratin materials, of synthetic or natural origin, the solubility of the pigments in water at 25 ° C and at atmospheric pressure (760 mm Hg) is less than 0.05% by weight, and preferably less than 0.01%;
- by "lacquermeans dyes adsorbed on insoluble particles, the resulting assembly remaining insoluble during use. The inorganic substrates on which the dyes are adsorbed are for example alumina, silica, calcium and sodium borosilicate or calcium and aluminum borosilicate, and aluminum. Among the organic dyes, mention may be made of cochineal carmine
- by "dyes» we mean oxidation dyes, and direct dyes used to color material fibers, in particular human fibers such as skin or hair.
- by dispersion or compositionanhydrous“means a dispersion or composition containing less than 2% by weight of water, or even less than 0.5% of water, and in particular free of water; where appropriate, such small amounts of water can in particular be supplied by ingredients of the composition which can contain residual amounts thereof;
- by "special effect pigmentsmeans pigments that generally create a colored appearance (characterized by a certain shade, a certain liveliness and a certain clarity) that is not uniform and changes according to the conditions of observation (light, temperature, viewing angles). observation…). They are thereby opposed to colored pigments which provide a uniform opaque, semi-transparent or transparent classic shade; And
- by "sub-micron"or in English"sub micronic» means pigments whose particle size has been micronized by the micronization method and whose average particle size is less than one micronmeter (μm), in particular between 0.1 and 0.9 μm, and preferably between 0.2 and 0.6 μm.
- The radical "aryl" Or "heteroaryl» or the aryl or heteroaryl part of a radical may be substituted by at least one substituent carried by a carbon atom, chosen from:
* a C alkyl radical₁-VS₆, preferably in C₁-VS₄, optionally substituted by one or more radicals chosen from hydroxyl, C-alkoxy₁-VS₂,(poly)-hydroxyalkoxy-C₂-VS₄, acylamino, amino substituted by two alkyl radicals, identical or different, in C₁-VS₄, optionally bearing at least one hydroxyl group or, the two radicals being able to form, with the nitrogen atom to which they are attached, a heterocycle comprising from 5 to 7 members, preferably from 5 or 6 members, optionally saturated or unsaturated substituted optionally comprising another heteroatom identical to or different from nitrogen;
* halogen;
* hydroxyl;
* C-alkoxy₁-VS₂;
* (poly)-hydroxyalkoxy C₂-VS₄;
*amino;
* an amino radical substituted by one or two alkyl radicals, identical or different, in C₁-VS₆optionally carrying at least one hydroxyl group,
* acylamino (-NR-C(O)-R') in which the radical R is a hydrogen atom, an alkyl radical in C₁-VS₄optionally carrying at least one hydroxyl group and the radical R' is a C alkyl radical₁-VS₂;
* carbamoyl ((R)₂N-C(O)-) in which the radicals R, identical or not, represent a hydrogen atom, an alkyl radical in C₁-VS₄optionally carrying at least one hydroxyl group;
* alkylsulfonylamino (R’-S(O)₂-N(R)-) in which the radical R represents a hydrogen atom, an alkyl radical in C₁-VS₄optionally carrying at least one hydroxyl group and the radical R' represents a C alkyl radical₁-VS₄, a phenyl radical;
* an aminosulfonyl radical ((R)₂N-S(O)₂-) in which the radicals R, identical or not, represent a hydrogen atom, an alkyl radical in C₁-VS₄optionally carrying at least one hydroxyl group;
* carboxylic in acid or salified form (preferably with an alkali metal or an ammonium, substituted or not);
* cyano;
* nitro or nitroso;
* polyhaloalkyl, preferably trifluoromethyl;
* the cyclic or heterocyclic part of a non-aromatic radical may be substituted by at least one substituent chosen from the groups: a) hydroxyl; b) C-alkoxy₁-VS₄, C-(poly)hydroxyalkoxy₂-VS₄; c) C-alkyl₁-VS₄;
* alkylcarbonylamino (R-C(O)-N(R')-) in which the radical R' is a hydrogen atom, an alkyl radical in C₁-VS₄optionally carrying at least one hydroxyl group and the radical R is a C alkyl radical₁-VS₂, amino optionally substituted by one or two identical or different C alkyl groups₁-VS₄themselves optionally bearing at least one hydroxyl group, said alkyl radicals being able to form, with the nitrogen atom to which they are attached, a heterocycle comprising from 5 to 7 members, saturated or unsaturated optionally substituted optionally comprising at least one other heteroatom different or not from nitrogen;
* alkylcarbonyloxy (R-C(O)-O-) in which the radical R is an alkyl radical in C₁-VS₄, amino group optionally substituted by one or two identical or different C alkyl groups₁-VS₄themselves optionally bearing at least one hydroxyl group, said alkyl radicals being able to form, with the nitrogen atom to which they are attached, a heterocycle comprising from 5 to 7 members, saturated or unsaturated optionally substituted optionally comprising at least one other heteroatom different or not from nitrogen;
* alkoxycarbonyl (R-G-C(O)-) in which the radical R is a C alkoxy radical₁-VS₄, G is an oxygen atom, or an amino group optionally substituted by a C-alkyl group₁-VS₄itself optionally bearing at least one hydroxyl group, said alkyl radical being able to form with the nitrogen atom to which they are attached, a heterocycle comprising from 5 to 7 membered, saturated or unsaturated optionally substituted optionally comprising at least one other heteroatom different or not from nitrogen;
- a cyclic or heterocyclic radical, or a non-aromatic part of an aryl or heteroaryl radical, can also be substituted by one or more oxo groups;
- a hydrocarbon chain is unsaturated when it contains one or more double bonds and/or one or more triple bonds;
- by "aryl“means a mono or polycyclic carbon group, condensed or not, comprising from 6 to 22 carbon atoms, and of which at least one ring is aromatic; preferentially the aryl radical is a phenyl, biphenyl, naphthyl, indenyl, anthracenyl, or tetrahydronaphthyl;
- by "heteroaryl"means a mono or polycyclic group, condensed or not, optionally cationic, comprising from 5 to 22 members, from 1 to 6 heteroatoms chosen from nitrogen, oxygen, sulfur and selenium atoms, and of which at least one ring is aromatic; preferably a heteroaryl radical is chosen from acridinyl, benzimidazolyl, benzobistriazolyl, benzopyrazolyl, benzopyridazinyl, benzoquinolyl, benzothiazolyl, benzotriazolyl, benzoxazolyl, pyridinyl, tetrazolyl, dihydrothiazolyl, imidazopyridinyl, imidazolyl, indolyl, isoquinolyl, naphthoimidazoly le, naphthooxazolyl, naphthopyrazolyl, oxadiazolyl, oxazolyl, oxazolopyridyl , phenazinyl, phenooxazolyl, pyrazinyl, pyrazolyl, pyrilyl, pyrazoyltriazyl, pyridyl, pyridinoimidazolyl, pyrrolyl, quinolyl, tetrazolyl, thiadiazolyl, thiazolyl, thiazolopyridinyl, thiazoylimidazolyl, thiopyrylyl, triazolyl, xanthylyl and its salt of ammonium;
- by "heterocyclic"means a radical which may contain one or more aromatic unsaturations, or non-aromatic, mono or polycyclic, condensed or not, containing from 5 to 22 members, comprising from 1 to 6 heteroatoms chosen from nitrogen, oxygen , and sulfur;
- by "heterocycloalkyl“means a saturated heterocyclic radical such as morpholinyl, piperazinyl, piperidinyl;
- by“salt of organic or mineral acidmore particularly means the salts chosen from a salt derived from a halogen acid such as i) hydrochloric acid HCl, ii) hydrobromic acid HBr, iii) sulfuric acid H₂N/A₄, iv) alkylsulfonic acids: Alk-S(O)₂OH such as methylsulfonic acid and ethylsulfonic acid; v) arylsulphonic acids: Ar-S(O)₂OH such as benzene sulfonic acid and toluene sulfonic acid; optionally hydroxylated carboxylic acids vi) such as citric acid; vii) succinic acid; viii) tartaric acid; ix) lactic acid, x) acetic acid CH₃C(O)OH; xi) alkoxysulfinic acids: Alk-O-S(O)OH such as methoxysulfinic acid and ethoxysulfinic acid; xii) aryloxysulfinic acids such as tolueneoxysulfinic acid and phenoxysulfinic acid; xiii) phosphoric acid H₃PO₄; xiv) triflic acid CF₃N/A₃H and xv) tetrafluoroboric acid HBF_4,more preferably theorganic or mineral acid saltsare chosen from salts of halogenated acids such as HCl and HBr, and optionally hydroxylated carboxylic acids such as vi) such as citric acid; vii) succinic acid; viii) tartaric acid; ix) lactic acid, x) acetic acid CH₃C(O)OH;
- by "anionic counterion» means an anion or an anionic group derived from an organic or mineral acid salt counterbalancing the charge of the molecule in question; more particularly the anionic counter-ion is chosen from i) halides such as chloride, bromide; ii) nitrates; iii) sulfonates including C₁-VS₆alkylsulphonates: Alk-S(O)₂O^-such as methylsulfonate or mesylate and ethylsulfonate; iv) arylsulphonates: Ar-S(O)₂O^-such as benzenesulfonate and toluenesulfonate or tosylate; v) citrate; vi) succinate; vii) tartrate; viii) lactate; ix) alkyl sulphates: Alk-O-S(O)O^-such as methysulfate and ethyl sulfate; x) arylsulphates: Ar-O-S(O)O^-such as benzene sulfate and toluene sulfate; xi) alkoxy sulphates: Alk-O-S(O)₂O^-such as methoxy sulfate and ethoxy sulfate; xii) aryloxy sulfates: Ar-O-S(O)₂O^-, xiii) phosphates O=P(OH)₂-O^- _,O=P(O^-)₂-OH O=P(O^-)₃, HO-[P(O)(O)^-)]_w-P(O)(O)^-)₂with w being an integer; xiv) acetate; xv) triflate; and xvi) borates such as tetrafluoroborate, xvii) disulfate disulfate (O=)₂N(O^-)₂or SO₄ ^2-and monosulphate HSO₄ ^-; the anionic counterion, derived from organic or mineral acid salt, ensures the electroneutrality of the molecule so it is understood that when the anion comprises several anionic charges then the same anion can be used for the electroneutrality of several cationic groups in the same molecule or else can be used for the electroneutrality of several molecules; for example a molecule that contains two cationic groups can contain either two anionic counter ions"monocharged"or either contains an anionic counterion"bicharged» such that (O=)₂N(O^-)₂ or O=P(O^-)₂-OH ;
- moreover, the addition salts that can be used in the context of the invention are chosen in particular from addition salts with a cosmetically acceptable base such as basifying agents as defined below such as alkali metal hydroxides such as soda, potash, ammonia, amines or alkanolamines;
- the expression "at least one» is equivalent to «one or more» ; And
- the limits of a domain of values are included in this domain, in particular in the expressions “between" And "from …
To …» ; And
the phrase "inclusivefor a range of concentrations means that the limits of the range are part of the defined interval.
- by "skinis meant within the meaning of the present invention the skin of the body and of the scalp, in particular the skin of the face, the neck and the hands.
- by« mature skinAccording to the invention, we mean in particular the skin of people who are at least 40 years old.
- by "very mature skinAccording to the invention, we mean in particular the skin of people who are at least 50 years old, in particular at least 60 years old, or even 65 years old.
- by "wrinkled» we mean a skin fold or static furrow visible to the eye which can be the result of the aging of keratin materials, in particular the skin, which can be caused by exposure or overexposure to UVA and UVB rays, smoke in particular from cigarettes, pollution air, hormonal decrease in estrogen, oxidative stress or not, or decrease in fat mass. Wrinkles can be on the face or on the body, preferably on the face. We can cite a) frontal wrinkles (transverse on the forehead), b) lion's wrinkles (between the eyebrows or the glabella, vertical between the two eyebrows), c) crow's feet wrinkles (peri-orbital wrinkles , outer corner of the eyes towards the ears), d) bitterness wrinkles (jugomental or labiomental groove, wrinkles located between the corners of the mouth to the chin), e) nasolabial folds (wrinkles vertical from the wings of the nose to the corners of the mouth), f) perioral wrinkles, or e) other facial wrinkles different from a) to f). Particularly the width of the groove is between 2.5 and 3 mm, the depth of the groove is preferably between 0.6 mm and 1 mm, and preferably the angle of the groove is between 20° and 40°, particularly between 30° and 40°.
- by "fine lines» we mean small wrinkles i.e. whose width of the furrow is particularly between 0.5 and 1 mm, preferably the depth of the furrow is between 0.4 and 1 mm, more particularly between 0.5 and 0.8 mm, even more particularly between 0.6 and 0.8 mm, and preferably the angle of the groove is between 10° and 40°, particularly between 20° and 30°.
- by "scar» we mean the part visible to the eye of a lesion resulting from the repair of the skin following an injury, a cut, burn, or incision for example.
- by "filling»means the visual reduction in the depth of the furrow or scar greater than or equal to 30%, preferably greater than or equal to 50%.
- by "oxidative stresswe mean all the damage caused by an increase in oxygen free radicals in a subject.

Dispersion (A)

The dispersion (A) of the invention comprises i) at least two polymeric particles of different chemical composition, preferably stabilized at the surface by ii) at least one stabilizing agent in a preferably anhydrous medium, further containing iii) at least one fatty liquid at 20°C and 1 hydrocarbon atmosphere, preferably volatile, iv) at least one polyol liquid at 20°C and 1 atmosphere, preferably chosen from (C ₂ -C ₆ )alkane-diol and (C ₂ -C ₆ )alkane-triol such as glycerol, and it may additionally contain v) water and optionally one or more cosmetic active ingredient(s) vi) different from iii) and iv) chosen from ingredients f) to j) as previously defined.
Dispersion (A) thus comprises i) at least two particle(s) of different chemical structure consisting of polymer(s) obtained by polymerization of monomers chosen from ethylenic monomers of:
a ₁ ) (C ₁ -C ₄ )(alkyl)acrylate of (C ₁ -C ₄ )alkyl whose (C ₁ -C ₄ )alkyl group(s) are optionally substituted by one or more groups chosen from hydroxy, (di )( ((C ₁ -C ₄ )alkyl)amino;
a ₂ ) poly[oxy(C ₁ -C ₄ )alkylene] (C ₁ -C ₄ )(alkyl)acrylate,
a ₃ ) ethylenic monomers comprising one or more carboxy, anhydride, phosphoric acid, sulphonic acid groups;
it being understood that each particle results from the polymerization of one or more ethylenic monomer(s) a ₃ ).

According to a particular form of the invention, the dispersion (A) comprises at least one particle i1) consisting of copolymer derived from monomers a ₁ ) and/or a ₂ ) and a ₃ ) and at least one particle i2) of chemical composition different from i1) chosen from a copolymer derived from monomers a ₁ ) and/or a ₂ ) and a ₃ ), a copolymer derived from monomers a ₃ ), a homopolymer derived from monomers a ₃ ).
According to a particular form of the invention, the dispersion (A) according to the invention comprises i) at least two particle(s) of different chemical composition comprising one or more polymer(s) chosen from:
a) copolymers of ethylenic monomers of:
a ₁ ) (C ₁ -C ₄ )(alkyl)acrylate of (C ₁ -C ₄ )alkyl whose (C ₁ -C ₄ )alkyl group(s) are optionally substituted by one or more groups chosen from hydroxy, (di )(C ₁ -C ₄ )(alkyl)amino; and or
a ₂ ) poly[oxy(C ₁ -C ₄ )alkylene] (C ₁ -C ₄ )(alkyl)acrylate, and
a ₃ ) ethylenic monomers comprising one or more carboxy, anhydride, phosphoric acid, sulphonic acid groups;
Or
b) mixtures of:
b ₁ ) at least one copolymer of ethylenic monomers of:
a ₁ ) (C ₁ -C ₄ )(alkyl)acrylate of (C ₁ -C ₄ )alkyl whose (C ₁ -C ₄ )alkyl group(s) are optionally substituted by one or more groups chosen from hydroxy, (di )(C ₁ -C ₄ )(alkyl)amino; and or
a ₂ ) poly[oxy(C ₁ -C ₄ )alkylene] (C ₁ -C ₄ )(alkyl)acrylate, and
a ₃ ) ethylenic monomers comprising one or more carboxy, anhydride, phosphoric acid, sulphonic acid groups; And
b ₂ ) at least one polymer of ethylenic monomers comprising one or more carboxy, anhydride, phosphoric acid, sulphonic acid groups

In order to obtain the dispersion (A), it is proposed to polymerize specific monomers capable of forming the particles i) in the presence of a polymeric random stabilizing agent ii) in at least one liquid fatty substance at 20°C and 1 atmosphere preferably volatile hydrocarbon iii) and optionally iv) at least one polyol which is liquid at 20°C and 1 atmosphere, preferably chosen from (C ₂ -C ₆ )alkane-diol and (C ₂ -C ₆ )alkane-triol such as glycerol and v) optionally water.

According to a particular embodiment of the invention, the dispersion (A) is such that the particles i) consist of i several copolymers derived from monomers a ₁ ), and/or a ₂ ) and a ₃ ) a) of chemical composition different or of mixtures of copolymers b ₁ ) with at least one polymer b ₂ ), as defined above, and ii) of one or more polymeric stabilizing agent(s) derived from polymer d) and/or from copolymers e) as defined above, and iv) one or more polyol(s) liquid(s) at 20°C and 1 atmosphere, preferably chosen from (C ₂ -C ₆ )alkane-diol and (C ₂ - C ₆ )alkane-triol such as glycerol, said dispersion possibly also comprising one or more cosmetic active agent(s) vi) as defined previously.

The dispersions (A) according to the invention consist of particles i), generally spherical, and ii) of at least one stabilizing agent, in a mixture iii) of hydrocarbon-based liquid fatty substance(s), v) optionally of water, in the presence iv) of at least one polyol which is liquid at 20°C and 1 atmosphere, preferably chosen from (C ₂ -C ₆ )alkane-diol and (C ₂ -C ₆ )alkane-triol such as glycerol, said dispersion possibly also comprising one or more cosmetic active ingredient(s) vi) as defined above.

According to another particular embodiment of the invention, the dispersion (A) is such that the particles i) consist of several copolymers derived from monomers a ₁ ), and/or a ₂ ) and a ₃ ) a) of chemical composition different or of mixtures of copolymers b ₁ ) with at least one polymer b ₂ ), as defined above, and ii) of one or more polymeric stabilizing agent(s) derived from polymer d) and/or from copolymers e) as defined above, and iv) one or more polyol(s) liquid(s) at 20°C and 1 atmosphere, preferably chosen from (C ₂ -C ₆ )alkane-diol and (C ₂ - C ₆ )alkane-triol such as glycerol, as well as v) water, said dispersion possibly further comprising one or more cosmetic active ingredient(s) vi) as defined previously.

The stabilizing agent(s) ii) is (are) particularly in the dispersion (A) in an amount of between 0.01% and 30% by weight relative to the total weight of the dispersion (A), more particularly between 0.1 % and 20% by weight, preferably between 0.5 and 10% by weight, more preferably between 0.6 and 8%, in particular between 0.7% and 4.5% by weight relative to the total weight of said dispersion (AT).

According to a particular embodiment of the invention, the amount of stabilizing agent(s) ii) is between 0.05% and 30% by weight relative to the total weight of said composition (A) without v) water , preferably between 0.2% and 20% by weight, especially between 2% and 15% by weight, more preferably between 2% and 10, especially between 2.5 and 5% by weight relative to the total weight of said dispersion (A) without v) water.

According to a particular embodiment of the invention, the amount of stabilizing agent(s) ii) is between 0.01% and 20% by weight relative to the total weight of said composition (A) comprising water, preferably between 0.1% and 15% by weight, especially between 0.9% and 10% more preferably between 1% and 5% especially between 2 and 3.5% relative to the total weight of said dispersion (A) comprising v) water.

According to a particular embodiment of the invention ii) the stabilizing agent(s) is found in an amount of between 5% and 40% by weight relative to the total weight of the ingredients i) + ii), more particularly between 8% and 30 % by weight, preferably between 9% and 20% by weight relative to the total weight of ingredients i) + ii).

Preferably, the constituent monomers of the particles i) are chosen from monomers which are insoluble in the liquid hydrocarbon-based medium consisting of iii) hydrocarbon-based liquid fatty substance(s). The insoluble monomers represent in particular 80% to 100% by weight, preferably 90% to 100% by weight, more preferably 95% to 100% by weight, even more preferably 100% by weight, of the total weight of the monomers forming the particles ( s).

Polymer particles i)
According to a particular embodiment of the invention, the particles i) of the dispersion (A) is (are) made up of at least two, preferably two polymer(s) chosen from a) the copolymers of ethylenic monomers of:
a ₁ ) (C ₁ -C ₄ )(alkyl)acrylate of (C ₁ -C ₄ )alkyl whose (C ₁ -C ₄ )alkyl group(s) are optionally substituted by one or more groups chosen from hydroxy, (di )( ((C ₁ -C ₄ )alkyl)amino; and/or
a ₂ ) poly[oxy(C ₁ -C ₄ )alkylene] (C ₁ -C ₄ )(alkyl)acrylate, and
a ₃ ) ethylenic monomers comprising one or more carboxy, anhydride, phosphoric acid, sulphonic acid groups
According to another particular embodiment of the invention, the particles i) of the dispersion (A) consist(s) of several polymer(s) chosen from
b ₁ ) at least one copolymer of ethylenic monomers of:
a ₁ ) (C ₁ -C ₄ )(alkyl)acrylate of (C ₁ -C ₄ )alkyl whose (C ₁ -C ₄ )alkyl group(s) are optionally substituted by one or more groups chosen from hydroxy, (di )( ((C ₁ -C ₄ )alkyl)amino; and/or
a ₂ ) poly[oxy(C ₁ -C ₄ )alkylene] (C ₁ -C ₄ )(alkyl)acrylate, and
a ₃ ) ethylenic monomers comprising one or more carboxy, anhydride, phosphoric acid, sulphonic acid groups; And
b ₂ ) at least one polymer of ethylenic monomers comprising one or more carboxy, anhydride, phosphoric acid or sulphonic acid groups.

Preferably, the ethylenic monomers comprising one or more carboxy, anhydride, phosphoric acid, sulphonic acid a ₃ ) groups are chosen from ethylenic monomers comprising one or more carboxy groups, more preferably (C ₁ -C ₄ )(alkyl)acrylic acids such as (meth)acrylic acid, in particular acrylic acid.

Preferably, the ethylenic monomers of (C ₁ -C ₄ )(alkyl)acrylate of (C ₁ -C ₄ )alkyl denote (meth)acrylate of (C ₁ -C ₄ )alkyl such as (meth)acrylate of ethyl or methyl (meth)acrylate, in particular methyl acrylate and ethyl acrylate.

Preferably, the (C ₁ -C ₄ )(alkyl)acrylate (C ₁ -C ₄ )alkyl ethylenic monomers in which the (C ₁ -C ₄ )alkyl group(s) are substituted by one or more groups chosen from hydroxy , (di)((C ₁ -C ₄ )alkyl)amino are chosen from ethylenic monomers of (C ₁ -C ₄ )(alkyl)acrylate (C ₁ -C ₄ )alkyl substituted by a hydroxy group or by a group (di)((C ₁ -C ₄ )alkyl)amino.According to one embodiment, the ethylenic monomers of (C ₁ -C ₄ )(alkyl)acrylate of (C ₁ -C ₄ )alkyl whose (C ₁ -C ₄ )alkyl groups are substituted by one or more hydroxy groups, are substituted by a hydroxy group such as 2-hydroxyethyl (meth)acrylate, in particular 2-hydroxyethyl acrylate (HEA).
According to another embodiment, the ethylenic monomers of (C ₁ -C ₄ )(alkyl)acrylate of (C ₁ -C ₄ )alkyl whose (C ₁ -C ₄ )alkyl group or groups are substituted by one or more (di)((C ₁ -C ₄ )alkyl)amino groups, are substituted by a di(C ₁ -C ₄ )alkyl)amino group such as a dimethylamino group such as 3-(dimethylamino)propyl (meth)acrylate , 2-(dimethylamino)ethyl (meth)acrylate.

According to a particular embodiment of the invention, the particles i) of the dispersion (A) contain particles A1 consisting of copolymers of ethylenic monomers:
a ₁ ) (C ₁ -C ₄ )(alkyl)acrylate of (C ₁ -C ₄ )alkyl whose (C ₁ -C ₄ )alkyl group(s) are optionally substituted by one or more groups chosen from hydroxy, (di )((C ₁ -C ₄ )alkyl)amino; and or
a ₂ ) poly[oxy(C ₁ -C ₄ )alkylene] (C ₁ -C ₄ )(alkyl)acrylate, and
a ₃ ) ethylenic monomers comprising one or more carboxy, anhydride, phosphoric acid, sulphonic acid groups,
preferably consisting of copolymers of ethylenic monomers a ₁ ) and a ₃ ), or a ₂ ) and a ₃ ), more preferably a ₁ ) and a ₃ ).

According to a particular embodiment of the invention, the particles i) of the dispersion (A) contain particles A′1 consisting of copolymers of ethylenic monomers a′ ₁ ) (C ₁ -C ₄ )(alkyl) acrylate of ( C ₁ -C ₄ )alkyl and a ₃ ) ethylenic monomers comprising one or more carboxy, anhydride, phosphoric acid, sulfonic acid,

According to another particular embodiment of the invention, the particles i) of the dispersion (A) contain particles A′2 consisting of copolymers of ethylenic monomers a′′ ₁ ) (C ₁ -C ₄ )(alkyl) acrylate of (C ₁ -C ₄ )alkyl substituted by one or more groups chosen from hydroxy, (di)((C ₁ -C ₄ )alkyl)amino, preferably substituted by a hydroxy group such as 2-hydroxyethylacrylate (HEA) and a ₃ ) ethylenic monomers comprising one or more carboxy, anhydride, phosphoric acid, sulphonic acid groups.

According to a preferred embodiment, the particles i) of the dispersion (A) contain particles A'1 and particles A'2 as described previously and more preferably the particles i) of the dispersion (A) are a mixture of particles A'1 and A'2 , in particular in a mass ratio (mass of particles A'1 /mass of particles A'2 ) of between 0.3 and 3, more particularly between 0.5 and 2.8, again more preferably between 0.6 and 2.

According to another particular embodiment of the invention, the particles i) of the dispersion (A) consist(s) of a mixture of b ₁ ) at least one copolymer of ethylenic monomers of a ₁ ) and/ or a ₂ ) and a ₃ ) as described previously and b ₂ ) at least one polymer of ethylenic monomers comprising one or more carboxy, anhydride, phosphoric acid or sulphonic acid groups.

According to another particular embodiment of the invention, the particles i) of the dispersion (A) consist(s) of a mixture of b ₁ ) at least one copolymer of ethylenic monomers of a ₁ ) and a ₃ ) as described previously and from b ₂ ) at least one polymer of ethylenic monomers comprising one or more carboxy, anhydride, phosphoric acid or sulphonic acid groups.

According to a particular form of the invention, b ₂ ) denotes a homopolymer of ethylenic monomers comprising one or more carboxy, or anhydride, or phosphoric acid or sulphonic acid groups, preferably comprising a carboxy group, more preferably of acid (meth) acrylic and even more preferably acrylic acid.

. The particles i) can be crosslinked or uncrosslinked.
According to one embodiment of the invention, the particles i) contain ethylenic copolymers A'1 resulting from the polymerization of monomer of formula (I) with ethylenic monomers comprising one or more carboxy, anhydride, phosphoric acid, sulfonic acid a ₃ ).

: Formula (I) in which:
- R representing a hydrogen atom or a (C ₁ -C ₄ )alkyl group such as methyl, and
- R′ representing a (C ₁ -C ₄ )alkyl group such as methyl or ethyl, preferably C ₁ -C ₄ alkyl acrylate such as methyl acrylate.

According to a particular embodiment of the invention, the (C ₁ -C ₄ )(alkyl)acrylate (C ₁ -C ₄ )alkyl monomers denote the C ₁ -C ₄ alkyl (meth)acrylate monomers preferably chosen from methyl (meth)acrylate, ethyl (meth)acrylate, n-propyl (meth)acrylate, isopropyl (meth)acrylate, n-butyl (meth)acrylate, ( isobutyl meth)acrylate, tert-butyl (meth)acrylate and more preferably chosen from methyl (meth)acrylate, ethyl (meth)acrylate.

and even more preferably chosen from methyl acrylate and ethyl acrylate.

According to an advantageous embodiment of the invention, the dispersion (A) comprises from 60% to 99% by weight, in particular from 70% to 99% by weight, preferably from 80% to 95% by weight, in particular from 85% to 93% by weight of monomers constituting the particles i) relative to the total weight of polymers contained in said dispersion (A).

Preferably, the monomers capable of forming the particles i) are chosen from monomers which are insoluble in the hydrocarbon-based liquid fatty substance(s) iii) of the dispersion (A).

The insoluble monomers preferably represent from 80 to 100% by weight, more preferably from 90 to 100% by weight, even more preferably from 95% to 100% by weight and even more particularly 100% by weight, of the total weight of the monomers forming particles i).

Ethylene monomers with acid or anhydride function:

The particles i) comprise ethylenic polymers comprising or being constituted by ethylenic monomers a ₃ ) comprising one or more carboxy, anhydride, phosphoric acid or sulphonic acid groups.

More particularly, the ethylenic monomers a ₃ ) comprising one or more carboxy, anhydride, phosphoric acid or sulphonic acid groups are chosen from (1) , (2) , (3) and (4) :
(1) R ¹ (R ² )C=C(R ³ )-Acid with R ¹ , R ² and R ³ representing a hydrogen atom or a CO ₂ H, H ₂ PO ₄ , or SO ₃ H group, and Acid representing a carboxy, phosphoric acid, sulphonic acid, preferably carboxy group, as well as its salts of organic or mineral bases such as alkalis or alkaline-earths, such as C(O)ONa or C(O)OK, preferably (1) represents (5) H ₂ C=C(R)-C(O)-OH with R representing a hydrogen atom, or a (C ₁ -C ₄ ) alkyl group such as methyl, as well as its salts organic or inorganic bases such as alkalis or alkaline-earth metals, such as Na or K;
(2) H ₂ C=C(R)-C(O)-N(R')-Alk-Acid with R and R', which are identical or different, represent a hydrogen atom, or a group (C ₁ -C ₄ ) alkyl; Alk represents a (C ₁ -C ₆ )alkylene group optionally substituted by at least one group chosen from Acid as defined above and hydroxy; and Acid is as defined previously, preferably carboxy or sulphonic acid as well as their salts of organic or inorganic bases such as alkali metals or alkaline-earth metals such as C(O)ONa or C(O)OK;
(3) Ar-(R ^a )C=C(R ^b )-R ^c with R ^a , R ^b and R ^c , identical or different, representing a hydrogen atom or a (C ₁ -C ₄ )alkyl group , and Ar represents an aryl group, preferably benzyl, optionally substituted by at least one CO ₂ H, H ₂ PO ₄ or SO ₃ H acid group, preferably substituted by a CO ₂ H or SO ₃ H group, as well as its salts of organic or mineral bases such as alkali metals or alkaline-earth metals, such as C(O)ONa or C(O)OK;
(4) Maleic anhydride of formula (4a) and (4b): Formulas (4b) and (4b) in which R _a , R _b and R _c , identical or different, representing a hydrogen atom or a (C ₁ -C ₄ )alkyl group, preferably R _a , R _b , and R _c represent a hydrogen atom. Preferably, an ethylenically unsaturated anhydride monomer of the invention is of formula (4b) and more preferably is maleic anhydride; And
more particularly the ethylenic monomer a ₃ ) comprising one or more carboxy, anhydride, phosphoric acid or sulphonic acid groups is chosen from (1) and (4) , in particular (5) and more particularly (5) and even more preferentially the acrylic acid.

According to another particular embodiment of the invention, the polymer constituting the particles i) andA'1and/or b₁) is an ethylenic acrylate copolymer resulting from the polymerization:
- at least one monomer a₁) of formula(I)as defined above, preferably C-alkyl acrylate₁-VS₄such as methyl acrylate, ethyl acrylate; And
- at least one monomer a₃) of formula(5)as previously defined as well as its salts of organic or mineral bases such as alkaline or alkaline-earth metals such as Na or K.

According to this embodiment, the amount of acrylic acid varies from 0.01% to 30% by weight relative to the total weight of the copolymer A'1 or b ₁ ), preferably between 0.1% to 20% by weight relative to the weight of the polymer(s) of the particles i More particularly A'1 or b ₁ ), is in particular a copolymer resulting from the copolymerization of acrylic acid with one or more alkyl (meth)acrylate monomers in C ₁ -C ₄ in particular chosen from methyl (meth)acrylate and ethyl (meth)acrylate.

According to another preferred embodiment of the invention, the polymer constituting the particles i) and in particularA'1and/or b₁) is an ethylenic acrylate copolymer resulting from the polymerization:
- at least two monomers a₁) different formula(I)as previously defined, preferably C-alkyl (meth)acrylate₁-VS₄such as methyl (meth)acrylate, ethyl (meth)acrylate; And
- a monomer a₃) of formula(5)as previously defined as well as its salts of organic or mineral bases such as alkalis or alkaline earth metals such as Na or K, preferably acrylic acid. Even more preferentiallyA'1and/or b₁) is derived from the polymerization of methyl acrylate, ethyl acrylate, and acrylic acid.

Preferably, the ethylenic monomer a ₃ ) comprising one or more carboxy, anhydride, phosphoric acid or sulphonic acid groups is a (C ₁ -C ₄ )(alkyl)acrylic acid, more particularly A'1 and/or b ₁ ) is ( are) copolymers of (meth)acrylate of (C ₁ -C ₄ )alkyl and of (meth)acrylic acid.

According to one embodiment, the ethylenic monomer a ₃ ) comprising one or more carboxy, anhydride, phosphoric acid or sulphonic acid groups is chosen from crotonic acid, maleic anhydride, itaconic acid, fumaric acid, maleic acid, styrenesulfonic acid, vinylbenzoic acid, vinylphosphoric acid, acrylic acid, methacrylic acid, acrylamidopropanesulfonic acid, acrylamidoglycolic acid, and their salts, even more preferentially the ethylenic monomer comprising one or more carboxy, anhydride, phosphoric acid, sulfonic acid groups represents acrylic acid and its salts.

According to one embodiment of the invention, the dispersion comprises at least 2 different types of particles, preferably 2 to 5 types of particles, more preferably two different types of particles.

According to one embodiment of the invention, the dispersion comprises at least 2 types of particles i) different, preferably 2 types of particles which are copolymers of different chemical structure derived from monomers a ₁ ) and/or a ₂ ) and a ₃ ), in particular which are copolymers of different chemical structure obtained by polymerization of monomers a ₁ ) and a ₃ ).

According to this embodiment, the different particles i) preferably comprise ethylenic copolymers ( IA ) of:
a'' ₁ ) (C ₁ -C ₄ )(alkyl)acrylate (C ₁ -C ₄ )alkyl in which the (C ₁ -C ₄ )alkyl group(s) are substituted by one or more groups chosen from hydroxy, ( di)( ((C ₁ -C ₄ )alkyl)amino, preferably hydroxy and/or
a ₂ ) poly[oxy(C ₁ -C ₄ )alkylene] (C ₁ -C ₄ )(alkyl)acrylate, and
a ₃ ) ethylenic monomers comprising one or more carboxy, anhydride, phosphoric acid, sulphonic acid, preferably carboxy groups; preferably ethylenic copolymers of _a''1 ) and _a3 ).

More particularly, the ethylenic monomers a ₃ ) comprising one or more carboxy, anhydride, phosphoric acid or sulphonic acid groups are chosen from (1) , (2) , (3) and (4) as defined above and denote in particular (5 ) as well as its salts of organic or mineral bases such as alkalis or alkaline-earth metals such as Na or K .

According to this particular embodiment of the invention, the particles i) different, preferably comprise i) ethylenic copolymers(I'A)from polymerization:
- To'''₁) of at least one monomer of formula(I') H ₂ C=C(R)-C(O)-O-R''Formula(I')in which :
-Rrepresenting a hydrogen atom or group (C₁-VS₄)alkyl such as methyl, and
-R''representing a group (C₁-VS₄)alkyl substituted by one or more hydroxy groups, (preferably the alkyl group is substituted at the end of the chain by a hydroxy group), such as hydroxymethyl or 2-hydroxyethyl, preferably (I') represents (meth)acrylate hydroxy-C₁-VS₄such as hydroxyethyl acrylate; And
- a3’’) of at least one monomer of formula(5)as previously defined as well as its salts of organic or mineral bases such as alkali or alkaline-earth such as Na or K, preferably acrylic acid.

According to yet another particular embodiment of the invention, the different particle(s) i) preferably comprise an ethylenic copolymer(IB)from polymerization:
- To₂’’) of at least one monomer of formula(I') H ₂ C=C(R)-C(O)-O-[ALK-O] _p -R'Formula(I'')in which :
-Rrepresenting a hydrogen atom or group (C₁-VS₄)alkyl such as methyl, and
-R'representing a group (C₁-VS₄)alkyl such as methyl or ethyl, preferably C-alkyl acrylate₁-VS₄such as methyl acrylate.
-ALKrepresents a group (C₁-VS₆) alkylene optionally substituted by at least one group chosen from Acid as defined above and hydroxy, preferably ALK represents a group (C₁-VS₄) alkylene such as ethylene, propylene, butylene, isobutylene, more preferably ALK represents an ethylene group;
- p represents an integer greater than or equal to 1, preferably less than or equal to 100; And
- a3’’) of at least one monomer of formula(5)as previously defined as well as its salts of organic or mineral bases such as alkali or alkaline-earth such as Na or K, preferably acrylic acid.

According to this embodiment, the different particle(s) i) preferably comprise ethylenic copolymers(IC)from the polymerization of:
To'''₁) monomers (C₁-VS₄(C) )(alkyl)acrylate₁-VS₄) alkyl preferably of formula(I)previously defined; and/or of
To₂) monomers (C₁-VS₄poly[oxy(C) )(alkyl)acrylate₁-VS₄)alkylene], and
To₃) ethylenic monomers comprising one or more carboxy, anhydride, phosphoric acid, sulphonic acid groups, preferably chosen from (1),(2),(3), And(4)as defined previously, more particularly of formula(5)as well as its salts of organic or mineral bases such as alkalis or alkaline earth metals such as Na or K and even more preferably acrylic acid,
preferably ethylene copolymers(IC)from the polymerization of monomers a’’’₁) and has₃), the a’’’ monomers₁) preferably denoting C-alkyl (meth)acrylates₁-VS₄in particular ethyl (meth)acrylate, methyl (meth)acrylate, more preferably methyl acrylate, ethyl acrylate.
More preferentially, the copolymers(IC) are derived from the polymerization of several a’’’ monomers₁) different and of monomers a₃), even more preferably ethyl (meth)acrylate with methyl (meth)acrylate and monomers a₃), more particularly methyl acrylate with ethyl acrylate and monomers a₃).

According to another embodiment of the invention, the dispersion comprises at least 2 different types of particles, preferably 2 different types of particles which are chosen from copolymers obtained by polymerization of monomers a ₁ ) and a ₃ ) as defined above , and b ₂ ) polymers of ethylenic monomers comprising one or more carboxy, anhydride, phosphoric acid, sulphonic acid, preferably carboxy, groups.
According to this embodiment, the copolymers are preferably chosen from the copolymers (IC) as described above .
The polymers of ethylenic monomers b ₂ ) preferably designate the homopolymers (ID), more preferably a homopolymer of monomers chosen from ( 1) , (2) , (3) and (4) as defined previously, more particularly of monomers of formula (5) as well as its salts of organic or inorganic bases such as alkali metals or alkaline-earth metals such as Na or K and even more preferentially of acrylic acid.

The polymer particle(s) i), of the dispersion (A) has (have) preferably a number-average size of greater than 50 nm.

The final size of the particles i) of structure (ID) included in the dispersion (A) is preferably greater than 50 nm. In particular a number-average size ranging from 50 nm and 600 nm; more particularly ranging from 100 nm to 500 nm, even more particularly ranging from 150 nm to 400 nm.

The final size of the particles i) of structure (IA) , (IB) , (IC) or (IE) included in the dispersion (A) is preferably greater than 100 nm. In particular a number-average size ranging from 100 nm and 100 mm; more particularly ranging from 500 nm to 10 mm.

The average particle size is determined by conventional methods known to those skilled in the art. A MALVERN model NanoZS laser particle sizer (particularly well suited to submicronic dispersions) is used to measure the size distribution of these samples. The operating principle of this type of device is based on dynamic light scattering (DLS), also called quasi-elastic light scattering (QELS) or photon correlation spectroscopy (PCS). It is also possible to determine the particle size by transmission microscopy

The sample is pipetted into a single-use plastic tank (4 transparent sides, 1 cm side and 4 mL capacity) placed in the measuring cell. The data are analyzed on the basis of a cumulant method which leads to a unimodal particle size distribution characterized by an average diameter in intensity d(nm) and a polydispersity factor in sizes Q. The results can also be expressed in the form of data statistics such as D10; D50 (median), D90 and mode.

Other granulometry techniques make it possible to obtain this type of information, such as analysis of individual particle tracking (Nanoparticle Tracking Analysis, NTA), laser diffraction (DL), acoustic extinction spectroscopy (AES) , Doppler velocimetry by spatial filter or image analysis.

The stabilizing agent(s) ii)

The dispersion (A) according to the invention also comprises one or more stabilizing agents ii). Preferably only one type of stabilizer ii) is used in the invention.

According to another particular embodiment of the invention, the stabilizer(s) ii) are chosen from d) ethylenic polymers of (C ₁ -C ₆ )(alkyl)acrylate (C ₃ -C ₁₂ )cycloalkyl monomers, preferably ethylenic homopolymers of (C ₁ -C ₆ )(alkyl)acrylate (C ₃ -C ₁₂ )cycloalkyl monomers, more preferably homopolymers of (meth)acrylate (C ₃ -C ₁₂ )cycloalkyl; more particularly ethylenic homopolymers resulting from the polymerization of monomers of formula: H ₂ C=C(R)-C(O)-O-R'' with R as defined previously, and R'' representing a group (C ₅ -C ₁₀ )cycloalkyl such as norbornyl, or isobornyl, preferably isobornyl.

More particularly, the stabilizing agent(s) ii) consists of ethylenic polymers chosen from ethylenic homopolymers d) resulting from the polymerization of monomers of the following formula:
[Chem. 3]

H2C=C(R)-C(O)-O-R’’’

with R representing a hydrogen atom or a (C ₁ -C ₄ )alkyl group such as methyl, and R''' representing a (C ₅ -C ₁₀ )cycloalkyl group such as norbornyl, or isobornyl, preferably isobornyl.

According to a particular embodiment of the invention, the stabilizing agent(s) ii) are chosen from e) copolymers of ethylenic monomers of (C ₁ -C ₆ )(alkyl) cycloalkyl acrylate (C ₃ -C ₁₂ ), and e2) (C ₁ -C ₄ )(alkyl)acrylate (C ₁ -C ₄ )alkyl, preferably copolymers of (meth)acrylate (C ₃ -C ₁₂ ) cycloalkyl and (meth) (C ₁ -C ₄ )alkyl acrylate.

According to another embodiment, the stabilizing agent(s) ii) are chosen from e′) the ethylenic copolymers of e1) (C ₁ -C ₆ )(alkyl) cycloalkyl acrylate (C ₃ -C ₁₂ ), and of e2 ) (C ₁ -C ₄ )(alkyl)acrylate (C ₁ -C ₄ )alkyl, preferably the copolymers e'1) of (meth)acrylate of (C ₃ -C ₁₂ ) cycloalkyl and e'2) (C ₁ -C ₄ )alkyl (meth)acrylate.

More particularly, the stabilizing agent(s) ii) are chosen from ethylenic copolymers e) of monomers of formula (IV) and of monomers of formula (III) : Formulas (III) and (IV) in which
- R , identical or different, representing a hydrogen atom or a (C ₁ -C ₄ )alkyl group such as methyl;
- Identical or different R′ representing a (C ₁ -C ₄ )alkyl group such as methyl or ethyl; And
- R'' representing a (C ₅ -C ₁₀ )cycloalkyl group such as norbornyl, or isobornyl, preferably isobornyl.

According to another particular embodiment of the invention , R'' represents a (C ₅ -C ₁₀ )cycloalkyl group such as norbornyl, or isobornyl, preferably isobornyl

According to a particular embodiment, the stabilizing agent(s) ii) of the invention consists of ethylenic copolymers e) chosen from e) copolymers of monomers e ₁ ) (C ₁ -C ₆ (C ₃ -C ₁₂ )cycloalkyl (alkyl)acrylate, in particular of formula (IV) and the monomers e ₂ ) of formula (III) as defined above.

According to another particular embodiment, the stabilizing agent(s) ii) of the invention consists of ethylenic copolymers d) chosen from copolymers of (C ₁ -C ₆ )(alkyl) (C ₃ -C ₁₂ )cycloalkyl acrylate in particular of formula (IV) .

According to another particular embodiment, the stabilizing agent(s) ii) of the invention is (are) constituted by ethylenic homopolymers d) chosen from homopolymers of monomers (C ₁ -C ₆ )(alkyl ) (C ₃ -C ₁₂ )cycloalkyl acrylate in particular of formula (IV) .

More particularly, the stabilizing agent(s) ii) of the invention consist(s) of ethylenic copolymers e) chosen from e'1) norbornyl (meth)acrylate, or isobornyl (meth)acrylate preferably isobornyl (meth)acrylate and methyl (meth)acrylate or ethyl (meth)acrylate.

According to another embodiment, the stabilizing agent(s) ii) are chosen from ethylenic copolymers e) resulting from the polymerization e1) of a monomer of formula (IV) as defined previously and e2) two different monomers of formula (III ) as previously defined.

Preferably, the stabilizing agent(s) ii) are chosen from copolymers resulting from the polymerization of e1) 1 monomer of formula (IV) as defined above, in particular chosen from isobornyl (meth)acrylates and e2) from 2 monomers different from formula (III) as defined above in particular different C ₁ -C ₄ alkyl (meth)acrylates preferably chosen from methyl acrylate and ethyl acrylate.

In particular, the stabilizing agent ii) is chosen from d) homopolymers of (C ₁ -C ₆ )(alkyl)acrylate (C ₃ -C ₁₂ )cycloalkyl monomers; and e) the random copolymers of e1) (C ₁ -C ₆ )(alkyl)acrylate of (C ₃ -C ₁₂ )cycloalkyl and e2) (C ₁ -C ₄ )(alkyl)acrylate of (C ₁ -C ₄ ) alkyl with a weight ratio e1/e2 greater than 4. Advantageously, said weight ratio ranges from 4.5 to 19. More advantageously, said weight ratio e1/e2 ranges from 5 to 15, more preferably said weight ratio ranges from 5, 5 to 14.

More particularly, the stabilizing agent ii) is a polymer chosen from d') the homopolymer of isobornyl (meth)acrylate and e) the random copolymers e1') of isobornyl (meth)acrylate and of e2') of C _{1 -C} 4 alkyl (meth)acrylate preferably present in a weight ratio of isobornyl (meth)acrylate/C ₁ -C ₄ alkyl (meth)acrylate (e1'/e2') greater _than 4. Advantageously, said weight ratio e1'/e2' ranges from 4.5 to 19. Advantageously, said weight ratio e1'/e2' ranges from 5 to 15, more preferably said weight ratio e1'/e2' ranges from 5, 5 to 14.

The stabilizing agent(s) ii) as defined above preferably comprise 80% to 100% by weight of monomer soluble in liquid hydrocarbon fatty substances iii), in particular from 85% to 95% by weight of soluble monomer, alone or as a mixture, relative to the total weight of monomers of the stabilizing agent(s). The stabilizing (co)polymer(s) ii) particularly comprises between 0% and 20% by weight, in particular between 5% and 15% by weight of monomer insoluble in hydrocarbon liquid fatty substances iii) , alone or as a mixture relative to the total weight of monomers of the stabilizing agent(s).

Preferably, the stabilizing agent(s) ii) and the particle(s) i) exhibit(s) a number-average molecular weight (Mn) of between 1,000 and 1,000,000 g/mol, in particular between 5,000 and 500 000 g/mol and even better between 10,000 and 300,000 g/mol.

The dispersion (A) according to the invention is ultimately formed of polymer particles, of fairly large diameter , i.e. preferably greater than 50 nm, and leads to deposits of compounds (C), film-forming, and resistant to fatty substances at room temperature. (25°C), and particularly interesting for make-up and/or hair applications.

According to a particular embodiment of the invention, the dispersion (A) comprises from 5% to 40% by weight, in particular 7% to 20%, in particular from 8% to 15% by weight, preferably from 9% to 13 % by weight of monomers (C ₁ -C ₆ )(alkyl)acrylate of (C ₃ -C ₁₂ )cycloalkyl d) or e1), relative to the total weight of polymers contained in said dispersion.

The liquid hydrocarbon fatty substance(s) iii)

The dispersion of polymer particles (A) according to the invention also comprises iii) one or more hydrocarbon-based liquid fatty substances in which said particles are dispersed.

According to a particular embodiment, the hydrocarbon-based liquid fatty substance(s) iii) of the invention is (are) chosen from hydrocarbons, in particular alkanes, oils of animal origin, oils of plant origin, glycerides or fluorinated oils of synthetic origin, fatty alcohols, fatty acid and/or fatty alcohol esters, non-silicone waxes, silicones; in particular the liquid hydrocarbon fatty substance(s) are preferably volatile hydrocarbon oils or are a mixture of different volatile oils, more particularly isododecane .

The liquid hydrocarbon fatty substances iii) are chosen in particular from C ₆ -C ₁₆ hydrocarbons or having more than 16 carbon atoms up to 50 carbon atoms, preferably between C ₆ and C ₁₆ , and in particular alkanes, oils of animal origin, oils of vegetable origin, glycerides, fatty alcohols, fatty acid and/or fatty alcohol esters, silicones.

It is recalled that within the meaning of the invention, alcohols, fatty acid esters more particularly have one or more hydrocarbon groups, linear or branched, saturated or unsaturated, comprising 6 to 50 carbon atoms, optionally substituted, in particular by one or more hydroxyl groups (in particular 1 to 4). If they are unsaturated, these compounds can comprise one to three carbon-carbon double bonds, conjugated or not.

As regards the C ₆ -C ₁₆ alkanes, the latter are linear, branched, possibly cyclic. By way of example, mention may be made of hexane, decane, undecane, dodecane, tridecane, isoparaffins such as isohexadecane, isodecane isododecane, and their mixtures such as the combination of undecane and tridecane, for example CETIOL UT®, or mixtures of C ₉ -C ₁₂ alkanes, preferably of natural origin, in particular linear or branched C ₉ -C ₁₂ alkanes. This latter mixture is in particular known under the INCI name C ₉ -C ₁₂ ALCANE E511470, CAS 68608-12-8, VEGELIGHT SILK® marketed by BioSynthIs. This biodegradable, volatile oil mixture obtained from coconut oil (viscosity is 0.9-1.1 cSt (40°C) and a flash point at 65°C).

The linear or branched hydrocarbons with more than 16 carbon atoms can be chosen from paraffin oils, petroleum jelly, petroleum jelly, polydecenes, hydrogenated polyisobutene such as Parléam.

Among the liquid hydrocarbon fatty substances iii) having an overall solubility parameter according to the HANSEN solubility space of less than or equal to 20 (MPa) ^1/2 , mention may be made of oils, which can be chosen from natural or synthetic oils , hydrocarbons, , optionally branched, alone or as a mixture.

According to a very advantageous embodiment, the dispersion (A) according to the invention comprises one or more liquid fatty substances which is (are) one or more hydrocarbon oil(s). The hydrocarbon oil(s) may be volatile or non-volatile.

According to a preferred embodiment of the invention, the hydrocarbon-based liquid fatty substance(s) are hydrocarbon-based oils which are volatile or are a mixture of different volatile oils .

According to a preferred embodiment of the invention, the fatty substance(s) are hydrocarbon oils, linear or branched, which are volatile, chosen in particular from undecane, dodecane, isododecane, tridecane, and their mixture of different oils. , volatiles preferably comprising isododecane in the mixture, or a mixture of undecane and tridecane

According to another particular embodiment, the liquid fatty substance(s) c) are a mixture of a volatile hydrocarbon-based oil and a non-volatile hydrocarbon-based oil, the mixture of which preferably comprises dodecane or isododecane as volatile oil.

According to another advantageous embodiment of the invention, the liquid hydrocarbon fatty substance(s) of the invention is (are) a mixture of non-volatile oil(s) and oil( s) volatile(s) preferably the mixture comprises as volatile oil undecane, dodecane, isododecane, tridecane, more preferably isododecane. As a volatile and non-volatile oil mixture, mention may be made of the mixture of isododecane and isononyl isononanoate.

More preferably when the fatty substance(s) are a mixture of volatile and non-volatile oil, the quantity of volatile oil is greater than the quantity of non-volatile oil

According to another particular embodiment, the liquid hydrocarbon fatty substance(s) iii) are a mixture of a volatile oil and a non-volatile oil such as an isododecane/octyldodecanol mixture or an isododecane/isononyl isononanoate mixture.

The hydrocarbon oil can be chosen from:
hydrocarbon oils having from 8 to 14 carbon atoms, and in particular:
- C branched alkanes₈-VS₁₄like C isoalkanes₈-VS₁₄of petroleum origin (also called isoparaffins) such as isododecane (also called 2,2,4,4,6-pentamethylheptane), isodecane, and for example the oils sold under the trade names of Isopars' or Permetyls ,
- linear alkanes, for example such as n-dodecane (C₁₂) and n-tetradecane (C₁₄) sold by Sasol respectively under the references PARAFOL 12-97 and PARAFOL 14-97,as well as their mixtures, the undecane-tridecane mixture, mixtures of n-undecane (C₁₁) and n-tridecane (C₁₃) obtained in Examples 1 and 2 of application WO 2008/155059 from Cognis, and mixtures thereof.
- hydrocarbon oils of plant origin such as triglycerides consisting of esters of fatty acids and glycerol, the fatty acids of which may have chain lengths varying from C₄to C₂₄, the latter possibly being linear or branched, saturated or unsaturated; these oils are in particular triglycerides of heptanoic acid or of octanoic acid, or even wheat germ, sunflower, grape seed, sesame, corn, apricot, castor, shea, avocado, olive, soy, sweet almond, palm, rapeseed, cotton, hazelnut, macadamia, jojoba, alfalfa, poppy, pumpkin, sesame, squash, rapeseed, blackcurrant, evening primrose, millet, barley, quinoa, rye, safflower, bancoulier, passionflower, muscat rose; shea butter; or caprylic/capric acid triglycerides such as those sold by Stéarineries Dubois or those sold under the names Miglyol 810^®, 812^®and 818^®,
- synthetic ethers having 10 to 40 carbon atoms;
- linear or branched hydrocarbons, of mineral or synthetic origin such as petroleum jelly, polydecenes, hydrogenated polyisobutene such as Parleam ®, squalane, paraffin oils, and mixtures thereof,
- esters such as oils of formula R¹C(O)-O-R² in which R¹represents the residue of a linear or branched fatty acid containing from 1 to 40 carbon atoms and R² represents a hydrocarbon chain in particular branched containing from 1 to 40 carbon atoms provided that R¹+R² either greater than or equal to 10, such as Purcellin's oil (cetostearyl octanoate), isopropyl myristate, isopropyl palmitate, C alcohol benzoates₁₂to C₁₅, hexyl laurate, diisopropyl adipate, isononyl isononanoate, 2-ethyl-hexyl palmitate, isostearyl isostearate, 2-hexyl-decyl laurate, 2- octyl-decyl, 2-octyl-dodecyl myristate, heptanoates, octanoates, decanoates or ricinoleates of alcohols or polyalcohols such as propylene glycol dioctanoate; hydroxylated esters such as isostearyl lactate, di-isostearyl malate, 2-octyl-dodecyl lactate; polyol esters and pentaerythritol esters, more preferably linear or branched C fatty acid esters₈-VS₁₀and C fatty alcohol₁₂-VS₁₈linear or branched alone or mixed with alkanes resulting from the hydrogenation / complete reduction of fatty acids from Cocos Nucifera (Coconut) oil, particularly dodecane or mixtures of cococaprylate / caprate with dodecane, mention may be made of those with the INCI name coconut alkanes (and) Coco-caprylate/caprate marketed under the name VEGELIGHT 1212LC® by Grant Industries.
- fatty alcohols that 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, oleic alcohol, 2-hexyldecanol, 2-butyloctanol, and 2-undecylpentadecanol.

Dispersion (A) in addition to the liquid hydrocarbon fatty substance, may comprise a silicone oil. If silicone oil is in the dispersion (A), preferably it is in an amount which does not exceed 10% by weight relative to the weight of the dispersion (A), more particularly in an amount less than 5% and more preferably 2%.

In particular, the dispersion (A) comprises at least one hydrocarbon-based liquid fatty substance iii) chosen from:
- vegetable oils formed by esters of fatty acids and polyols, in particular triglycerides, such as sunflower, sesame or rapeseed, macadamia, soybean oil, sweet almond oil, calophyllum, palm, grapeseed, corn, arara, cotton, apricot, avocado, jojoba, olive or cereal germ;
- linear, branched or cyclic esters, having more than 6 carbon atoms, in particular 6 to 30 carbon atoms; and in particular isononyl isononanoate;
and more particularly the esters of formula R ^d -C(O)-OR ^e in which R ^d represents the residue of a higher fatty acid comprising from 7 to 19 carbon atoms and R ^e represents a hydrocarbon chain comprising from 3 to 20 carbon atoms, such as palmitates, adipates, myristates and benzoates, especially diisopropyl adipate and isopropyl myristate;
- hydrocarbons and in particular linear, branched and/or cyclic alkanes, volatile or non-volatile, such as C ₅ -C ₆₀ isoparaffins, possibly volatile such as isododecane, Parleam (hydrogenated polyisobutene), isohexadecane, cyclohexane, or 'ISOPARs'; or paraffin oils, petroleum jelly, or hydrogenated polyisobutylene; especially isododecane,
- ethers having 6 to 30 carbon atoms;
- aliphatic fatty monoalcohols having 6 to 30 carbon atoms, the hydrocarbon chain not comprising any substitution group, such as oleic alcohol, decanol, dodecanol, octadecanol, octyldodecanol and linoleic alcohol; in particular octyldodecanol;
- polyols having 6 to 30 carbon atoms, such as hexylene glycol; And
- mixtures thereof, such as the combination of undecane and tridecane such as CETIOL UT®, preferably isododecane, or mixtures of linear or branched C ₈ -C ₁₀ fatty acid esters and fatty alcohol in C ₁₂ -C ₁₈ and alkanes from the hydrogenation / complete reduction of mixtures of fatty acids from Cocos Nucifera (Coconut) oil, in particular dodecane such as mixtures of cococaprylate / caprate and dodecane , mention may be made of those with the INCI name coconut alkanes (and) Coco-caprylate/caprate marketed under the name VEGELIGHT 1212LC® by Grant Industries; or mixtures of C ₉ -C ₁₂ alkanes, whose chains comprise from 9 to 12 carbon atoms, preferably linear or branched alkanes, C ₉ -C ₁₂ in particular comprising dodecane, mention may be made of the mixture oil with INCI name C9-12 ALKANE, VEGELIGHT SILK® marketed by BioSynthIs.
.

Advantageously, the liquid hydrocarbon fatty substance(s) of the invention are apolar, i.e. formed solely from carbon and hydrogen atoms.

Preferably, the dispersion (A) comprises at least one liquid hydrocarbon fatty substance iii) apolar, preferably chosen from:
- linear or branched C ₈ -C ₃₀ alkanes, in particular C ₁₀ -C ₂₀ , more particularly C ₁₀ -C ₁₆ alkanes, volatile or non-volatile; preferably volatile
- cyclic, non-aromatic, C ₅ -C ₁₂ alkanes; volatile or non-volatile; preferably volatile, and
- their mixtures.

The hydrocarbon-based liquid fatty substance(s) are preferably chosen from hydrocarbon-based oils having from 8 to 16 carbon atoms, in particular having from 10 to 14 carbon atoms, preferably volatile, more particularly the apolar oils, described above.

Among the branched C ₈ -C ₁₆ alkanes, in particular C ₁₀ -C ₁₄ suitable as liquid hydrocarbon fatty substances iii) in the dispersion of the invention, mention may be made of:
- isoalkanes of petroleum origin (also called isoparaffins) such as isododecane (also called 2,2,4,4,6-pentamethylheptane), isodecane and for example the oils sold under the trade names of Isopars' or from Permetlys;
- linear alkanes, for example such as 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, the mixture undecane-tridecane, mixtures of n-undecane (C ₁₁ ) and n-tridecane (C ₁₃ ) from Cognis, and mixtures thereof.

Preferably, the liquid hydrocarbon fatty substance(s) iii) of the invention are apolar, more particularly isododecane.

According to another advantageous embodiment of the invention, the liquid hydrocarbon fatty substance(s) are a mixture of volatile oils or a mixture of one or more non-volatile oil(s) and volatile oil(s). (s) preferably the mixture comprises isododecane or an oil mixture in particular of undecane and tridecane as volatile oil and isononyl isononanoate and/or octyldodecanol as non-volatile oil.

Preferably, the liquid hydrocarbon fatty substance(s) iii) are present in the dispersion of the invention in an amount of between 1% and 25% by weight, more preferably between 2.5% and 20% by weight, even more preferably between 4% and 15% and preferably between 10 and 11.2% by weight relative to the total weight of said dispersion (A) with water v).

According to a particular embodiment of the invention, the liquid hydrocarbon fatty substance(s) iii) are found in the dispersion of the invention in an amount of between 1.5% and 30% by weight, more preferably between 4% and 20% by weight, even more preferably between 8 and 15% especially between 12% and 13% by weight relative to the total weight of said dispersion (A) free of water.

According to a particular embodiment of the invention, the ratio by weight of the sum of the ingredients [i) + ii)] / iii) is less than or equal to 3, more particularly [i) + ii]] / iii) the ratio mass is between 1 and 2.5, even more particularly is between 1.5 and 2.4, preferably between 1.7 and 2.2.

The polyol(s) iv)

The dispersion (A) of the invention also comprises one or more polyol(s) which are liquid(s) at 20° C. and 1 atmosphere.

By “ polyol ” is meant a compound that is liquid at 20° C. and 1 atmosphere, comprising at least 2 hydroxy groups, preferably between 2 and 10 hydroxy (OH) groups, and comprising at least one carbon atom. In particular, the polyol(s) of the invention is (are) chosen from compounds comprising at least 2 OH groups, preferably between 2 and 8 OH groups, more preferably 2 or 3 OH groups, even more preferably 3 OH groups and comprising a hydrocarbon chain, linear or branched, cyclic or acyclic, saturated or unsaturated, comprising from 1 to 10 carbon atoms, in particular between 2 and 8 carbon atoms.

More particularly the polyol(s) of the invention has (have) a molecular weight of between 50 g/mol and 300 g/mol, more particularly between 80 g/mol and 150 g/mol.

According to a particular embodiment of the invention, the polyol(s) iv) is (are) chosen from:
- hydrocarbon compounds (C ₂ -C ₆ )alkane-diol and
- (C ₂ -C ₆ )alkane-triol such as glycerol and butane triols, and pentane triols, and hexane triols such as hexane-1,2,6-triol.

Preferably, the polyol(s) iv) is (are) chosen from hydrocarbon compounds (C ₂ -C ₆ )alkane-triols such as glycerol.

According to a particular embodiment of the invention, the dispersion (A) comprises one or more polyol(s) iv) in an amount greater than or equal to 5% by weight and less than 95% by weight relative to the total weight of the water-free dispersion, particularly the amount of polyol(s) present in the dispersion is between 10% and 90% by weight relative to the total weight of the water-free dispersion, more particularly between 25% and 90% by weight, more particularly between 35% and 90% by weight, relative to the total weight of the dispersion (A) free of water and even more preferably between 50% and 70%.

According to another particular embodiment of the invention, the dispersion (A) comprises one or more polyol(s) in an amount greater than or equal to 15% by weight and less than 90% by weight relative to the total weight of the dispersion with water, particularly the amount of polyol(s) in the dispersion is between 20% and 85% by weight relative to the total weight of the dispersion with water, more particularly between 25% and 80% by weight , more particularly between 40% and 60% by weight, relative to the total weight of the dispersion (A) with water.

Possibly some water v)

According to a particular embodiment of the invention, the dispersion (A) in particular the hydrogel comprises water v) in particular in an amount of between 5% and 40% by weight relative to the total weight of the dispersion, plus particularly between 7% and 35% by weight, preferably between 10.8% and 26.0% by weight, relative to the total weight of the dispersion (A).

According to a particular embodiment of the invention, the ratio by weight of the hydrocarbon liquid(s) fatty substance(s) iii)/water v) is between 0.1 and 5, more particularly between 0.2 and 1, preferably between 0.3 and 0.7, more preferably between 0.4 and 0.6.

The water suitable for the invention can be tap water, distilled water, spring water, floral water, such as blueberry water and/or mineral water such as VITTEL water, LUCAS water or LA ROCHE POSAY water and/or thermal water.

Dispersion (A) may further comprise one or more water-miscible solvents.

By “ water-miscible solvent ” according to the present invention, is meant a compound that is liquid at room temperature and miscible with water (miscibility in water greater than 50% by weight at 25° C. and atmospheric pressure).

The water-miscible solvents that can be used in the dispersion (A) of the invention can also be volatile.

Among the water-miscible solvents that can be used in the composition or dispersion (A) according to the invention, mention may be made in particular of lower monoalcohols having from 2 to 5 carbon atoms such as ethanol and isopropanol,

The water can also comprise any water-soluble or water-dispersible compound compatible with an aqueous phase, such as additional film-forming polymers, surfactants and mixtures thereof.

By “ surfactant ” is meant a “ surfactant ” or “ surfactant ” which is a compound capable of modifying the surface tension between two surfaces, surfactants are amphiphilic molecules, ie which have two parts of different polarity, one lipophilic and apolar and the other hydrophilic and polar. Surfactants can be nonionic, anionic, amphoteric, cationic or nonionic active.

According to a preferred embodiment of the invention, the dispersion (A) of the invention does not comprise more than 3% by weight of surfactants relative to the total weight of the dispersion, preferably not more than 2% by weight of surfactants per relative to the total weight of the dispersion, more particularly not more than 1% by weight of surfactants relative to the total weight of the dispersion, even more preferably the dispersion (A) does not comprise more than 0.5% by weight of surfactants per relative to the total weight of the dispersion, even better the mixture (A) does not comprise any surfactant.

Optionally one or more cosmetic active ingredients vi)

According to a particular embodiment of the invention, the dispersion of the invention (A) comprises one or more cosmetic active ingredient(s) vi) different from iii) and from iv), chosen from f) dyes, g) pigments; h) active ingredients for caring for keratin materials and i) UV (A) and/or UV (B) screening agents as well as m) mixtures thereof.

According to a preferred embodiment of the present invention, the cosmetic active ingredient(s) of the invention is (are) chosen from g) pigments.

According to a particular embodiment of the present invention, the cosmetic active ingredient(s) of the invention is (are) chosen from h) active ingredients for the care of keratin materials, preferably active ingredients for the care of the skin in particular antioxidants or moisturizers in particular polar different from iv).

By “ moisturizer ” is meant a compound which fixes water, which allows the hydration of keratin materials, making it possible to prevent and/or fight more effectively against the signs of skin dryness. On the other hand, the term "moisturizing" does not cover substances having only an emollient effect, such as petroleum jelly and vegetable or silicone oils, which are compounds which deposit an occlusive lipid film on the skin preventing the evaporation of the water.

In particular, the dispersion (A) comprises one or more moisturizers different from iv), which are hygroscopic substances which cause rehydration of the skin by uptake of atmospheric water and by retention of water in keratin materials, in particular the skin .

Mention may be made, as moisturizers, of the constituents of the NMF (Natural Moisturizing Factor), which are compounds of small water-soluble molecules with high hygroscopic power playing a moisturizing role.

The NMF mainly consists of a) amino acids (preferably in an amount by weight of between 50% and 80% such as 65%), b) of organic acids (preferably in an amount by weight of between 10 and 30% such as 21%) including pyrrolidone carboxylic acid, c) ions (anions or cations, in an amount by weight between 3 and 10% such as 8%), d) urea (in an amount by weight between 1% and 6 % such as 4%) and e) of sugars (in quantity by weight between 1% and 4% such as 2%, it being understood that the % being relative to the total weight of a) + b) + c) + d) + e) ).

Mention may in particular be made of organic acids and preferably (poly)hydroxylated carboxylic acids and their salts.

According to a particular embodiment of the invention, the ingredient(s) vi) are chosen from (poly)hydroxylated carboxylic acids. More particularly, carboxylic acids are (poly)hydroxylated hydrocarbon compounds comprising from 2 to 20 carbon atoms, saturated or unsaturated, cyclic or acyclic, comprising one or more carboxy or carboxylate groups, and one or more hydroxy groups, and optionally comprising a or more heteroatoms such as nitrogen.

Among the (poly)hydroxylated carboxylic acids, mention may in particular be made of lactic acid and the lactate of an alkaline salt such as sodium [72-17-3], optionally unsaturated (C ₁ -C ₂₀ ) carboxylic acids such as linoleic acid [60-33-3], heteroarylcarboxylic acids such as pyrrolidonecarboxylic acid, in particular 2-pyrrolidinone-5-carboxylic acid (PCA) [98-79-3],

The solid organic (poly)hydroxy compound(s) at 20°C and at one atmosphere vi) are organic polyols different from polyols having from 4 to 8 carbon atoms, miscible with water as defined above.

According to another particular embodiment of the invention, the ingredient(s) vi) are chosen from amino acids, in particular chosen from alanine, arginine, aspartic acid, citrulline, glutamic acid, urocanic acid, glycine, histidine, leucine, lysine, ornithine, phenylalanine, proline, serine, threonine, tryptophan, tyrosine, valine, and their salts and mixtures thereof. Glycine and serine are preferred.

According to another variant of the invention, the ingredient(s) vi) are chosen from GAG glycosaminoglycans and their sulfates. These include: hyaluronic acid or hyaluronan (HA), heparan sulfate (HS), heparin (HP), chondroitin, chondroitin sulfate (CS), chondroitin 4-sulfate or chondroitin sulfate A (CSA ), chondroitin 6-sulfate or chondroitin sulfate C (CSC), dermatan sulfate or chondroitin sulfate B (CSB), keratan sulfate (KS) which differs from other glycosaminoglycans by the presence of galactose instead of uronic acid , and dextran sulphate. Mention may also be made of chitosan. Hyaluronic acid and its sodium salt are preferred.

Another category of moisturizers according to the invention consists of urea [57-13-6] and derivatives such as hydroxyalkyl ureas in particular of general formula (VII) :

[Chem. 7]
R ₁ R ₂ NC(O)-NR ₃ R ₄ (VII)
Formula (VII) in which R ₁ , R ₂ , R ₃ and R ₄ each independently represent a hydrogen atom, a C ₁ -C ₄ alkyl group or a C ₂ -C ₆ hydroxyalkyl group which may contain from 1 to 5 hydroxyl groups, at least one of the radicals R ₁ -R ₄ representing a hydroxyalkyl group, and their salts, solvates such as hydrates and optical isomers.

Among the salts, mention may be made of the salts of mineral acids, such as sulfuric acid, hydrochloric acid, hydrobromic acid, hydriodic acid, phosphoric acid, boric acid. Mention may also be made of the salts of organic acids, which may comprise one or more carboxylic, sulphonic or phosphonic acid groups. They can be linear, branched or cyclic aliphatic acids or even aromatic acids. These acids may additionally comprise one or more heteroatoms chosen from O and N, for example in the form of hydroxyl groups. Mention may in particular be made of propionic acid, acetic acid, terephthalic acid, citric acid and tartaric acid.

By solvate is meant a stoichiometric mixture of said compound in question with one or more molecules of water or organic solvent, such a mixture being derived from the synthesis of said compound.

More particularly, the ingredient(s) vi) according to the invention consists of the acid

According to yet another particular embodiment of the present patent application, the cosmetic active ingredient(s) vi) of the invention is (are) chosen from i) antioxidants.

By " antioxidant " or AOX, we mean a natural or synthetic compound that decreases, slows down, or prevents the oxidation of other chemical substances in contact with it (see for example Antioxidants, C. Kröhnke et al. Ullmann's Encyclopedia of Industrial Chemistry Wiley -VCH Verlag GmbH & Co. KGaA, Weinheim 10.1002/14356007.a03_091.pub2, ISBN: 9783527306732| DOI: 10.1002/14356007 (2015)).

According to yet another particular embodiment of the present patent application, the cosmetic active ingredient(s) vi) of the invention is (are) chosen from i) UV(A) filters and/or UV(B) and their mixture.

According to a particular embodiment of the invention, the dispersion (A) comprises iv) one or more cosmetic active agents chosen from pigments.

The pigment(s) represent more particularly from 0.5 to 40% by weight of the total weight of the dispersion (A), and preferably from 1 to 20% by weight.

The pigments are solid, white or colored particles, naturally insoluble in the liquid hydrophilic and lipophilic phases usually used in cosmetics or rendered insoluble by formulation in the form of a lacquer, where appropriate. More particularly, the pigments are little or not soluble in aqueous-alcoholic media.

The pigments which can be used are in particular chosen from the organic and/or inorganic pigments known in the art, in particular those which are described in the encyclopedia of chemical technology by Kirk-Othmer and in the encyclopedia of industrial chemistry by Ullmann. Mention may in particular be made, as pigments, of organic and inorganic pigments such as those defined and described in Ullmann's Encyclopedia of Industrial Chemistry "Pigment organics", 2005 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim 10.1002/14356007.a20 371 and ibid, "Pigments, Inorganic, 1. General” 2009 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim10.1002/14356007.a20_243.pub3

These pigments can be in the form of powder or pigment paste. They can be coated or uncoated.

The pigments can for example be chosen from mineral pigments, organic pigments, lakes, special effect pigments such as nacres or glitter, and mixtures thereof.

The pigment can be an inorganic pigment. By mineral pigment, we mean any pigment that meets the definition of the Ullmann encyclopedia in the chapter inorganic pigment. Mention may be made, among the mineral pigments useful in the present invention, of iron or chromium oxides, manganese violet, ultramarine blue, chromium hydrate, ferric blue and titanium oxide.

The pigment may be an organic pigment.

By organic pigment, we mean any pigment that meets the definition of the Ullmann encyclopedia in the organic pigment chapter.

The organic pigment can in particular be chosen from nitroso, nitro, azo, xanthene, quinoline, anthraquinone, phthalocyanine, compounds of metal complex type, isoindolinone, isoindoline, quinacridone, perinone, perylene, diketopyrrolopyrrole, thioindigo, dioxazine, triphenylmethane, quinophthalone.

More preferably, the active ingredient(s) vi) of the invention are chosen from:
- organic and mineral or inorganic pigments,
- special effect pigments such as fluorescent, thermochromic, photochromic pigments, nacres, coated or uncoated, in the form of powder or pigment paste, lacquers, glitter or mixtures thereof;
- said pigments can be dispersed in the product using a dispersing agent and the pigments can be surface-treated with an organic agent;
in particular, the cosmetic active ingredient(s) iv) is (are) chosen from:
- the organic pigments nitroso, nitro, azo, xanthene, quinoline, anthraquinone, phthalocyanine, of metal complex type, isoindolinone, isoindoline, quinacridone, perinone, perylene, diketopyrrolopyrrole, thioindigo, dioxazine, triphenylmethane, quinophthalone;
- white or colored organic pigments which are chosen from carmine, carbon black, aniline black, azo yellow, quinacridone, phthalocyanine blue, sorghum red, blue pigments codified in the Color Index under the BLUE 1 LAKE Cl 42090, 69800, 69825, 73000, 74100, 74160 pigment references, the yellow pigments coded in the Color Index under the Cl references 11680, 11710, 15985, 19140, 20040, 21100, 21108, 47000 , 47005, the green pigments codified in the Color Index under the references Cl 61565, 61570, 74260, orange pigments codified in the Color Index under the references CI 11725, 15510, 45370, 71105, red pigments codified in the Color Index under the references CI 12085 ,12120,12370,12420,12490,14700,15525,15580,15620,15630,15800,15850,15865,15880,17200,26100,45380,45410, 58000, 73360, 73915, 75470, pigments obtained by oxidative polymerization of indole or phenolic derivatives;
- mineral pigments or inorganic pigments chosen iron or chromium oxides, manganese violet, ultramarine blue, chromium hydrate, ferric blue and titanium oxide;
preferably, the cosmetic active ingredient(s) iv) is (are) chosen from carbon black, iron oxides, in particular red, brown or black, and micas coated with iron oxide, triarylmethane pigments, in particular blue and violet, such as BLUE 1 LAKE, azo pigments, in particular red, such as D&C RED 7 alkali metal salt of lithol red such as the calcium salt of lithol red B, more preferably the pigment(s) used are chosen from red iron oxides and azo pigments, in particular red ones, such as D&C RED 7, more preferably red iron oxides

According to a particular embodiment of the invention, the quantity of pigments varies from 0.5% up to 40%, and preferably from 1 to 20% relative to the weight of the dispersion (A) comprising them.

Optionally one or more cross-linking agent(s) vii)

According to a particular embodiment of the invention, the dispersion (A) of the invention comprises vii) one or more crosslinking agents.

• Areprésente un groupe (hétéro)aryle éventuellement substitué ou (hétéro)cycloalkyle éventuellement substitué, de préférence A représente un groupe phényle ;
• R ⁸ , identique ou différent, représente un atome d’hydrogène ou un groupe (C₁-C₈)alkyle, linéaire ou ramifié, éventuellement substitué, de préférence en C₁-C₆tel que méthyle ;
• X ¹ etX ² ,identiques ou différents, représentent un hétéroatome choisi parmi oxygène, soufre et amino N(R’’) avec R’’ étant un atome d’hydrogène ou un groupe (C₁-C₆)alkyle, linéaire ou ramifié; de préférence X¹= O ou NH, et X²= O ; et plus particulièrement X¹= X²= un atome d’oxygène,;
• Wreprésente : i) soit un groupeAtel que défini précédemment en particulier un groupe hétéroaryle à 5 ou 6 chainons tel que pyridinyle ou hétérocycloalkyle comprenant au moins un atome d’oxygène à de 5 à 8 chainons tel que tétrahydrofuryle, pipérazynyle ou hexahydrofuro[3,2-b]furanyle, ii) soit un groupe *-A-(CR ⁹ R ¹⁰ ) _x -A-*lorsque w vaut 2, avecAtel que défini précédemment,R ⁹ etR ¹⁰ , identique ou différents représentant un atome d’hydrogène ou un groupe (C₁-C₆)alkyle tel que méthyle, de préférence R⁹et R¹⁰= H,xreprésente un entier compris inclusivement entre 0 et 10, de préférence x = 1 et * représente le point d’attache aux groupes -X¹-C(X²)-C(=CH₂)-R⁸; iii) soit une chaine hydrocarbonée, linéaire ou ramifiée, polyvalente, de préférence di ou trivalente, saturée ou insaturée, de préférence saturée, éventuellement substituée de préférence par un groupe hydroxy, éventuellement interrompue par un ou plusieurs hétéroatomes tels que O, et comprenant de 1 à 20 atomes de carbone ;
• preprésente 0 ou 1;
• uetwreprésentent un entier compris inclusivement entre 2 et 10, plus particulièrement entre 2 et 5, tel que u = 2 et w = 2 ou 3.

De préférence le ou les réticulants sont de formule(VII), plus particulièrementWreprésente une chaine hydrocarbonée linéaire polyvalente saturée, éventuellement interrompue par un ou plusieurs atomes d’oxygène, comprenant de 1 à 20 atomes de carbone et w = 2 ou ou w = 3,.According to a particular embodiment of the invention, the crosslinking agent(s) is (are) chosen from the monomers of formula(VI)And(VII)next : (IV) (VII) Formulas(VI)And(VII)in which :

• A represents an optionally substituted (hetero)aryl or optionally substituted (hetero)cycloalkyl group, preferably A represents a phenyl group;
• R ⁸ , identical or different, represents a hydrogen atom or a (C ₁ -C ₈ )alkyl group, linear or branched, optionally substituted, preferably C ₁ -C ₆ such as methyl;
• X ¹ AndX ² ,identical or different, represent a heteroatom chosen from oxygen, sulfur and amino N(R'') with R'' being a hydrogen atom or a group (C₁-VS₆)alkyl, linear or branched; preferably x¹= O or NH, and X²= O ; and more particularly X¹=X²= an oxygen atom;
• W represents: i) either a group A as defined above, in particular a 5- or 6-membered heteroaryl group such as pyridinyl or heterocycloalkyl comprising at least one 5- to 8-membered oxygen atom such as tetrahydrofuryl, piperazynyl or hexahydrofuro[ 3,2- b ]furanyl, ii) or a group *- A- (CR ⁹ R ¹⁰ ) _x -A-* when w is 2, with A as defined previously, R ⁹ and R ¹⁰ , identical or different representing a hydrogen atom or a (C ₁ -C ₆ )alkyl group such as methyl, preferably R ⁹ and R ¹⁰ = H, x represents an integer comprised inclusively between 0 and 10, preferably x = 1 and * represents the point of attachment to the -X ¹ -C(X ² )-C(=CH ₂ )-R ⁸ groups; iii) either a hydrocarbon chain, linear or branched, polyvalent, preferably di or trivalent, saturated or unsaturated, preferably saturated, optionally substituted, preferably by a hydroxy group, optionally interrupted by one or more heteroatoms such as O, and comprising 1 to 20 carbon atoms;
• p represents 0 or 1 ;
• u and w represent an integer comprised inclusively between 2 and 10, more particularly between 2 and 5, such that u = 2 and w = 2 or 3.

Preferably, the crosslinker(s) are of the formula(VII), more particularlyWrepresents a saturated polyvalent linear hydrocarbon chain, optionally interrupted by one or more oxygen atoms, comprising from 1 to 20 carbon atoms and w = 2 or or w = 3,.

According to a preferred variant of the invention, the monomers of formula (VI) and (VII) are chosen from the compounds of the following table, as well as their optical and geometric isomers, their tautomers and acid or base salts, mineral or organic:

Name Abbreviation Structure Styrene/divinyl benzene (DVB) (VI ₁ ) Diisopropyl benzene (DIB) (VI ₂ ) 1,3-phenylene diacrylamide;
1,4-phenylene diacrylamide (VII ₁ ) N , N'- 1,3-phenylenebis(2-methyl-2-propenamide);
N , N'- 1,4-phenylenebis(2-methyl-2-propenamide) (VII ₂ ) 3,5-bisacrylamido-benzoic acid with R'' identical and equal to H; and 3,5-bismethylacrylamido-benzoic acid with R'' identical and equal to CH ₃ (VII ₃ )
R'' = H or (C ₁ -C ₄ )alkyl such as CH ₃ 2,6-bisacryloylamidopyridine with R'' identical and equal to H;
2,6-bismethylacryloyl-amidopyridine with R'' identical and equal to CH ₃ (VII ₄ )
R'' = H or (C ₁ -C ₄ )alkyl such as CH ₃ 1,4-diacryloylpiperazine with R'' identical and equal to H;
1,4-dimethylacryloylpiperazine with R'' identical and equal to CH ₃ (PAD) (VII ₅ )
R'' = H or (C ₁ -C ₄ )alkyl such as CH ₃ Di Ethylene Glycol Di Acrylate (n=2)
Diethylene Glycol Di Methacrylate (n=2)
n is an integer greater than or equal to 1 and preferably between 1 and 10 and preferably between 2 and 4 and preferably 2 (DEGDA)
(DEGDMA)
(VII ₆ )
R'' = H or (C ₁ -C ₄ )alkyl such as CH ₃ Ethylene glycol dimethacrylate with R'' identical and equal to CH ₃ (EGDMA); Ethylene glycol diacrylate with R'' identical and equal to H (EGDA)
(EGDMA)
(VII' ₆ )
R'' = H or (C ₁ -C ₄ )alkyl such as CH ₃ Tetramethylene dimethacrylate with R'' identical and equal to CH ₃ ; Tetramethylene diacrylate with R'' identical and equal to H (TDMA)
(VII ₇ )
R'' = H or (C ₁ -C ₄ )alkyl such as CH ₃ Hexamethylene dimethacrylate with R'' identical and equal to CH ₃ and Hexamethylene diacrylate with R'' identical and equal to H (VII ₈ )
R'' = H or (C ₁ -C ₄ )alkyl such as CH ₃ Anhydroerythritoldimethacrylate with R'' identical and equal to CH ₃ and Anhydroerythritoldiacrylate with R'' identical and equal to H (VII ₉ )
R'' = H or (C ₁ -C ₄ )alkyl such as CH ₃ 1,4;3,6-dianhydro-p-sorbitol-2,5-dimethacrylate with R'' identical and equal to CH ₃ ; 1,4;3,6-dianhydro-p-sorbitol-2,5-diacrylate with R'' identical and equal to H (VII ₁₀ )
R'' = H or (C ₁ -C ₄ )alkyl such as CH ₃ Isoproplenebis(1,4-phenylene)-dimethacrylate with R'' identical and equal to CH ₃ ; Isoproplenebis(1,4-phenylene)-diacrylate R'' identical and equal to H
(VII ₁₁ )
R'' = H or (C ₁ -C ₄ )alkyl such as CH ₃ 2,2-bis(Hydroxymethyl)butanol trimethacrylate with R'' identical and equal to CH ₃ (TRIM); 2,2-bis(Hydroxymethyl)butanol triacrylate R'' identical and equal to H (TRIMS)
(VII ₁₂ )
R'' = H or (C ₁ -C ₄ )alkyl such as CH ₃ Pentaerythritol triacrylate with R'' identical and equal to H; Pentaerythritol trimethacrylate with R'' identical and equal to CH ₃ (VII ₁₃ )
R'' = H or (C ₁ -C ₄ )alkyl such as CH ₃ Pentaerythritol tetraacrylate with R'' identical and equal to H (PETRA); Pentaerythritol tetramethacrylate with R'' identical and equal to CH ₃ (PETRA) (VII ₁₄ )
R'' = H or (C ₁ -C ₄ )alkyl such as CH ₃ N,O -bismethacryloyl-ethanolamine with R _c equal to ethylene and R'' identical and equal to CH ₃
(NOBE) (VII ₁₅ )
R _c = (C ₁ -C ₆ )alkylene such as ethylene
R'' = H (C ₁ -C ₄ )alkyl such as CH ₃ N,N'- methylene-bis-acrylamide with R _c =CH ₂ (MDAA); Or
N,N -1,2-ethanediylbis(2-methyl-2-propenamide)
N , N'- ethylene-bis-acrylamide with R _c =CH ₂ -CH ₂ ;
N , N'- butylene-bis-acrylamide with R _c =CH ₂ -CH ₂ -CH ₂ -CH ₂ ;
N , N'- hexylene-bis-acrylamide with R _c = _CH2 - _CH2 - _CH2 - _CH2 - _CH2 - _CH2 (MDAA)
(VII ₁₂ )
R _c = (C ₁ -C ₆ )alkylene
R'' = H or (C ₁ -C ₄ )alkyl such as CH ₃ In particular, the crosslinkers of the invention are chosen from(VII ₆ )such as(VII' ₆ ), (VII ₇ )And(VII ₈ ),such as Ethylene Glycol Diacrylate; Tetra(ethylene glycol) diacrylate, and diethylene glycol diacrylate (DEGDA), preferably DEGDA.

According to another particular embodiment of the invention, the crosslinking agent(s) is (are) chosen from homopolymers or copolymers derived from monomers of formula(VI)And(VII)as previously defined; preferably the homopolymers and copolymers resulting from monomer of formula(VII), more preferably withWrepresenting a C alkyl group₁-VS₁₀divalent and w = 2 or in C₁-VS₁₀trivalent and w = 3, said alkyl groups being optionally interrupted by one or more heteroatoms such as O, more preferably C-alkyl₁-VS₈divalent and w = 2. In particular homopolymers and copolymers derived from monomers chosen from(VII ₆ )such as(VII' ₆ ) , (VII ₇ )And(VII ₈ )such as THE Poly(Ethylene Glycol) Diacrylate such as Acrylate-PEG3500-Acrylate marketed by Aldrich JKA4048 and Multi arm Poly(Ethylene Glycol) Acrylate such as 4 arm-PEG10K-Acrylate marketed by Aldrich JKA7068; N,N'-Methylenebisacrylamide

Preferably, the crosslinker(s) of the invention are chosen from(VII ₆ ) )such as(VII' ₆ ),(VII ₇ )And(VII ₈ ),such as ethylene glycol diacrylate; diethylene glycol diacrylate; tetra(ethylene glycol) diacrylate; THE poly(ethylene glycol) diacrylate such as acrylate-PEG3500-acrylate; poly(ethylene glycol) multiarm acrylate; and the N,N'-methylenebisacrylamide; more preferably ethylene glycol diacrylate.
Optionally one or more neutralizers viii),

According to one embodiment, the dispersion (A) or the composition (B) used in the preparation of the dispersion (A) comprises at least one neutralizer viii) chosen in particular from organic or inorganic, preferably inorganic, alkaline agents, in particular hydroxides of alkali or alkaline-earth metals such as sodium or potassium hydroxide.

By “ neutralizing ” is meant any compound making it possible to neutralize the pH at a pH close to neutral pH, ie 7. To do this, an organic or inorganic acid, or an alkaline agent (also called a base), as defined below, can be used. after, in particular the hydroxides of alkali or alkaline-earth metals such as sodium or potassium hydroxide or of transition metals such as zinc.

More particularly, the neutralizer is added to composition (B) until the pH of said composition is obtained from 5 to 8, in particular 6.5 to 7.5 such as 7.

The inorganic (or inorganic) alkaline agent(s) are preferably chosen from ammonia, alkaline carbonates or bicarbonates such as sodium or potassium carbonates and sodium or potassium bicarbonates, sodium or potassium hydroxides or their mixtures.

According to one embodiment of the invention, the alkaline agent(s) are basic amino acids such as, for example, lysine or arginine. According to an advantageous embodiment of the invention, the alkaline agent(s) are organic amines, i.e. they contain at least one substituted (secondary or tertiary amine) or unsubstituted (primary amine) amine group.

The organic alkaline agent(s) are more preferably chosen from organic amines whose pK _b at 25° C. is less than 12, and preferably less than 10, even more advantageously less than 6. If the alkaline agent(s) comprise several groups amaine, this is the pK _b corresponding to the highest basicity function.

As hybrid compounds, mention may be made of the salts of the amines mentioned above with acids as defined above such as carbonic acid, hydrochloric acid.

• West un radical divalent alkylène en C₁-C₆éventuellement substitué par un groupement hydroxyle ou un radical alkyle en C₁-C₆, et/ou éventuellement interrompu par un ou plusieurs hétéroatomes tels que l’oxygène ou NR^u;
• R ^x ,R ^y ,R ^z R ^t etR ^u , identiques ou différents, représentent un atome d'hydrogène, un radical alkyle en C₁-C₆ou hydroxyalkyle en C₁-C₆, aminoalkyle en C₁-C₆.

The organic alkaline agent(s) are, for example, chosen from alkanolamines, oxyethylenated and/or oxypropylene ethylenediamines, amino acids and the compounds of formula (VIII) below:
(VIII)
Formula (VIII) in which:

• W is a divalent C ₁ -C ₆ alkylene radical optionally substituted by a hydroxyl group or a C ₁ -C ₆ alkyl radical, and/or optionally interrupted by one or more heteroatoms such as oxygen or NR ^u ;
• R ^x , R ^y , R ^z R ^t and R ^u , which are identical or different, represent a hydrogen atom, a C ₁ -C ₆ alkyl radical or a C ₁ -C ₆ hydroxyalkyl radical, a C ₁ -C ₆ aminoalkyl radical .

Mention may be made, by way of example of such amines, of 1,3 diaminopropane, 1,3 diamino 2 propanol, spermine, spermidine.

By “alkanolamine” is meant an organic amine comprising a primary, secondary or tertiary amine function, and one or more linear or branched C ₁ -C ₈ alkyl groups carrying one or more hydroxyl radicals.

Suitable in particular for carrying out the invention are alkanolamines such as mono-, di- or tri-alkanolamines, comprising one to three C ₁ -C ₄ hydroxyalkyl radicals, identical or not.

Among compounds of this type, mention may be made of monoethanolamine, diethanolamine, triethanolamine, monoisopropanolamine, diisopropanolamine, N-dimethylaminoethanolamine, 2-amino-2-methyl-1-propanol, triisopropanolamine, 2-amino -2-methyl-1,3-propanediol, 3-amino-1,2-propanediol, 3-dimethylamino-1,2-propanediol, tris-hydroxymethylaminomethane.

More particularly, the amino acids that can be used are of natural or synthetic origin, in their L, D or racemic form and comprise at least one acid function chosen more particularly from carboxylic, sulphonic, phosphonic or phosphoric acid functions. Amino acids can be in neutral or ionic form. As amino acids that can be used in the present invention, mention may in particular be made of aspartic acid, glutamic acid, alanine, arginine, ornithine, citrulline, asparagine, carnitine, cysteine , glutamine, glycine, histidine, lysine, isoleucine, leucine, methionine, N-phenylalanine, proline, serine, taurine, threonine, tryptophan, tyrosine and valine.

More particularly, the neutralizer(s) of the invention are chosen from:
* alkaline agents chosen in particular from mineral or inorganic alkaline agents such as LiOH, NaOH, KOH, Ca(OH) ₂ , NH ₄ OH or Zn(OH) ₂ ; And
* organic alkaline agents such as (C ₁ -C ₈ )alkylamines containing primary, secondary or tertiary amine group(s), in particular triethylamine or butylamine, or (C ₁ -C ₈ )alkylamines containing group(s) primary, secondary or tertiary comprising one or more nitrogen or oxygen atoms and/or comprising one or more hydroxy groups; mention may in particular be made of 2-amino-2-methylpropanol, triethanolamine and 2-dimethylamino-2-propanol. Mention may also be made of lysine or 3-(dimethylamino)propylamine.

Optionally one or more radical initiators ix)

• de type I dans laquelle les composés photoactifs vont entrainer, sous irradiation, une coupure unimoléculaire de la liaison covalente pour conduire à un composé radical libre également symbolisé par un “point”, et
• de type II dans laquelle les composés photoactifs sous irradiation, vont conduire à une réaction bimoléculaire dans lequel l’état excité des composés photoactifs intéragissent avec une seconde molécule (ou co-initateur) pour générer des radicaux libres.

According to a particular embodiment of the invention, the process for preparing the dispersion (A) and the material (C) uses one or more radical initiators.
By "radical initiator" is meant in particular the initiators of free radicals generated by thermal means or from light sources (see for exampleMacromol. Rapid Common. Christian Decker,23, 1067–1093 (2002);Encyclopedia of Polymer Science and Technology, “free radical photopolymerization” http://onlinelibrary.wiley.com/doi/10.1002/0471440264.pst490/pdf;ibid,
"light-curing, cationic",
http://onlinelibrary.wiley.com/doi/10.1002/0471440264.pst491/pdf;Macromol. Symp. 143 , 45-63 (1999)). These photoactive compounds are not chemical oxidizing agents such as peroxides including hydrogen peroxide or hydrogen peroxide generating systems. Two large families are to be distinguished:

• type I in which the photoactive compounds will cause, under irradiation, a unimolecular cleavage of the covalent bond to lead to a free radical compound also symbolized by a “dot”, and
• type II in which the photoactive compounds under irradiation will lead to a bimolecular reaction in which the excited state of the photoactive compounds interact with a second molecule (or co-initiator) to generate free radicals.

• R ₁ ,R ₂ ,R ₃ , etR ₄ , identiques ou différents, représentent un atome d’hydrogène ou un groupe (C₁-C₈)alkyle, linéaire ou ramifié, éventuellement substitué, (C₁-C₈)alkoxy, linéaire ou ramifié ; aryle éventuellement substitué tel que phényle ;

ou alors R₁et R₂et/ou R₃et R₄forment ensemble avec les atome de carbone qui les portent un (hétéro)cycloalkyle éventuellement substitué comprenant de 3 à 7 chainons, particulièrement (C₃-C₆)cycloalkyle tel que cyclohexyle ;
de préférenceR ₁ ,R ₂ ,R ₃ , etR ₄ , identiques ou différents, représentent un atome d’hydrogène ou un groupe (C₁-C₆)alkyle, linéaire ou ramifié ;
xety, identiques ou différents, représentent un entier compris inclusivement entre 0 et 6, de préférence x et y =0 ;

• R, etR’identiques ou différents, de préférence identiques, représentent i) un radical EA ou EA’ tels que définis ci-après, ou un groupe choisi ii) parmi (C₁-C₈)alkyle, linéaire ou ramifié, éventuellement substitué, iii) aryle éventuellement substitué, iv) aryl((C₁-C₈)alkyle éventuellement substitué,

ou alors R avec R₁et/ou R’ avec R₃forment ensemble avec l’atome de carbone qui les portent un groupe C(X¹) et R₂ et R₄étant tels que définis précédemment ou R₂ et R₄, identiques ou différents, représentent un groupeR ₅ -(X ² ) _w -dans lequel w vaut 0 ou 1, R₅représente un atome d’hydrogène, un groupe (C₁-C₈)alkyle, linéaire ou ramifié, un groupe (hétéro)aryle éventuellement substitué tel que phényle ou un groupe (hétéro)cycloalkyle éventuellement substitué notamment par une groupe (C₁-C₆)alkyle tel que cyclohexyle éventuellement substitué par une groupe (C₁-C₆)alkyle et X²est tel que défini ci après ;

• EAetEA’, identiques ou différents, de préférence identiques, représentent un groupe électroattracteur, de préférence électroattracteur par effet mésomère -M, tel que cyano,-C(X ¹ )-X ² -R _a , phosh(on)ate, sulf(on)ate, nitro, ou nitroso ; plus particulièrement EA = EA’ = CN ;
• X _a , identiques ou différents, représentent un hétéroatome choisi parmi oxygène et soufre, un groupe -C(O)-O- ou –O-C(O)-, un groupe -O-C(O)-O- ou –O-C(O)-O- ; de préférence X_areprésentent un atome d’oxygène ;

X ¹ , etX ² , identiques ou différents, représentant un hétéroatome choisi parmi oxygène, soufre et amino N(R’’) avec R’’ étant un atome d’hydrogène ou un groupe (C₁-C₆)alkyle, linéaire ou ramifié ; de préférence X¹et X²représentent un atome d’oxygène ; (C) (D) (E) (F) Formules(C),(D),(E)ou(F)dans lesquelles :

• Rreprésente un groupe choisi parmi :

i) (C₁-C₁₀)alkyle, éventuellement substitué, de préférence par un ou plusieurs atomes ou groupes choisis parmi halogène, hydroxy, (C₁-C₁₀)alkoxy, (hétéro)cycloalkyle comprenant entre 5 et 10 chainons tel que morpholinyle, et amino R_aR_bN- avec R_a, R_b, identiques ou différents, représentant un atome d’hydrogène ou une groupe (C₁-C₁₀)alkyle ou alors R_aet R_bforment ensemble avec l’atome d’azote qui les portent un groupe hétéroaryle ou hétérocycloalkyle tel que morpholino ;
ii) (C₁-C₁₀)alkoxy éventuellement substitué, de préférence par les mêmes substituants que pour i) (C₁-C₁₀)alkyle ;
iii) hydroxy ;
iv) (hétéro)aryle éventuellement substitué tel que phényle éventuellement substitué de formule(C’)
avecR’ ¹ , R’ ² , R’ ³ ,identiques ou différents, étant tels que définis pourR ¹ ,R ² ,R ³ et
représentant le point d’attache au reste de la molécule ;
v) (hétéro)cycloalkyle éventuellement substitué de préférence par un groupe hydroxy ou un groupe (C₁-C₁₀)alkyle;
vi) R⁴-(X)_n-C(X)-(X)_n’- avec R⁴représentant un groupe (C₁-C₁₀)alkyle éventuellement substitué, (hétéro)aryle éventuellement substitué tel que phényle éventuellement substitué de formule(C’), (hétéro)cycloalkyle éventuellement substitué, n et n’, identiques ou différents, vallant 0 ou 1;
vii) R_cR_dP(X)- avec R_creprésentant un groupe (C₁-C₁₀)alkyle éventuellement substitué, ou (hétéro)aryle éventuellement substitué, et R_dreprésentant un groupe (hétéro)aryle éventuellement substitué ;
viii) ou alors R¹avec R en ortho du groupe C(X)-R ou R’’ et R’’¹en ortho du groupe R’-Y⁺-R’’ forment ensemble avec les atomes qui les portent un (hétéro)cycle fusionné au phényle ou (hétéro)aryle fusionné au phényle éventuellement substitué notamment sur partie non aromatique par un ou plusieurs groupes oxo, ou thiooxo ; de préférence R¹avec R en ortho du groupe C(X)-R forment ensemble avec les atomes qui les portent et le cycle phényle fusionné un groupe anthraquinone(G) : (G)

• R ¹ ,R ² ouR ³ , identiques ou différents, représentent un i) atome d’hydrogène, ii) d’halogène tel que chlore, iii) un groupe (C₁-C₁₀)alkyle éventuellement substitué, iv) (C₁-C₁₀)alkoxy éventuellement substitué notamment par un groupe hydroxy, v) (hétéro)aryle éventuellement substitué, vi) (hétéro)cycloalkyle éventuellement substitué, vii) carboxy, viii) cyano, ix) nitro, x) nitroso, xi) -S(O)_p-OM avec p valant 1 ou 2, M représentant un atome d’hydrogène, un métal alcalin ou alcalino-terreux, xii) R⁴R⁵N- ; xiii) R⁴-(X)_n-C(X)-(X)_n’- avec R⁴, n et n’ tels que définis précédemment, R⁵est tel que défini pour R⁴ou alors R⁴et R⁵forment ensemble avec l’atome d’azote qui les portent un hétérocycloalkyle ou hétéroaryle éventuellement substitué tel que morpholino , identiques ou différents, vallant 0 ou 1, xiv) hydroxy, ou xv) thiol ;
• R’’ ¹ ,R’’ ² ouR’’ ³ , identiques ou différents, sont tels que définis pourR ¹ ,R ² ,R ³ , de préférence sont choisi parmi l’atome d’hydrogène ou R⁴-Y– avec R⁴étant tel que défini précédemment et de préférence un groupe phényle ;
• ou alorsRetR ¹ contigus,forment ensemble avec les atomes de carbone qui les portent un groupe (hétéro)cycloalkyle éventuellement insaturé et éventuellement substitué, de préférence cycloalkyle éventuellement substitué et en particulier par un ou plusieurs groupe oxo et/ou éventuellement fusionné par un groupe aryle tel que benzo ;
• ou alors deux substituants contigusR ¹ ,R ² et/ouR’ ¹ ,R’ ² forment ensemble un groupe dérivé d’anydryde maléique tel que –C(X)-X-C(X)– ;
• X, identique ou différent, représente un atome d’oxygène, de soufre ou un groupe NR⁵avec R⁵tel que défini précédemment, de préférence représentant un atome d’hydrogène ou un groupe (C₁-C₁₀)alkyle ; plus particulièrement X représente un atome d’oxygène ;
• Yest tel que défini pourX, de préférenceYreprésente un atome de soufre ;
• Métalreprésente un métal de transition tel que le fer ou chrome, de préférence Fe, ledit métal pouvant être cationique auquel cas l’initiateur de formule (D) comprend un nombre de contre-ion anioniqueAn ^- tel que défini précédemment, permettant d’atteindre l’électroneutralité de la molécule ;
• LetL’, identiques ou différents, représentant un ligand de métal de transition de préférence choisi parmi les donneurs d’électrons suivants C(X) avec X tel que défini précédemment, cyano CN, (C₁-C₆)alcènyle, (hétéro)aryle éventuellement substitué tel que bipyridinyle, amines telles que les amines R⁴R⁵R⁶N avec R⁴et R⁵tels que définis précédemment et R⁶représentant un atome d’hydrogène, ou un groupe tel que défini pour R⁴, phosphine R⁴R⁵R⁶P telle que les tri(hétéro)arylphosphine, (hétéro)cycloalkyle étant de préférence insaturé tel que cyclopentadiène, carbène comme les carbène d’arduengo,
• qreprésentant un entier compris inclusivement entre 1 et 6, permettant d’atteindre la stabilité du complexe métallique i.e. de façon à obtenir un nombre d’électron autour du Métal égal à 16 ou 18 électrons (on parle également de sphère de coordination à 16 ou 18 électrons), ;
• R’etR’’,identiques ou différents, représentent un groupe (hétéro)aryle éventuellement substitué ;
• An ^- représente un contre ion anionique tel que défini précédemment de préférence choisi parmi (Hal)₆P^-,ou (Hal)₆Sb^-,avec Hal, identiques ou différents, représentant un atome d’halogène tel que le fluor ; et
• R ^a ,R ^b ,R ^c ouR ^d , identiques ou différents, représentent un atome d’hydrogène ou un groupe (C₁-C₁₀)alkyle.

More particularly, the radical initiators are chosen from the compounds of formula(AT),(B),(VS),(D),(E), (W), as well as their organic or mineral acid salts, their optical, geometric and tautomeric isomers and their solvates such as hydrates:
(AT) (B) Formulas(AT)Or(B)in which :

• R ₁ , R ₂ , R ₃ , and R ₄ , which are identical or different, represent a hydrogen atom or a (C ₁ -C ₈ )alkyl group, linear or branched, optionally substituted, (C ₁ -C ₈ )alkoxy , linear or branched; optionally substituted aryl such as phenyl;

or else R₁and R₂and/or R₃and R₄form together with the carbon atoms which carry them an optionally substituted (hetero)cycloalkyl comprising from 3 to 7 members, particularly (C₃-VS₆)cycloalkyl such as cyclohexyl;
preferablyR ₁ ,R ₂ ,R ₃ , AndR ₄ , identical or different, represent a hydrogen atom or a group (C₁-VS₆) alkyl, linear or branched;
xAndthere, which are identical or different, represent an integer comprised inclusively between 0 and 6, preferably x and y=0;

• R , and R' which are identical or different, preferably identical, represent i) an EA or EA' radical as defined below, or a group chosen ii) from (C ₁ -C ₈ )alkyl, linear or branched, optionally substituted, iii) optionally substituted aryl, iv) optionally substituted aryl((C ₁ -C ₈ )alkyl,

or else R with R₁and/or R’ with R₃form together with the carbon atom that carries them a group C(X¹) and R₂ and R₄being as defined previously or R₂ and R₄, identical or different, represent a groupR ₅ -(X ² ) _w -where w is 0 or 1, R₅represents a hydrogen atom, a group (C₁-VS₈)alkyl, linear or branched, an optionally substituted (hetero)aryl group such as phenyl or an optionally substituted (hetero)cycloalkyl group, in particular by a group (C₁-VS₆)alkyl such as cyclohexyl optionally substituted by a group (C₁-VS₆)alkyl and X²is as defined below;

• EA and EA' , which are identical or different, preferably identical, represent an electron-withdrawing group, preferably an electron-withdrawing group through the -M mesomeric effect, such as cyano, -C(X ¹ )-X ² -R _a , phosh(on)ate, sulf(on)ate, nitro, or nitroso; more particularly EA=EA′=CN;
• X _a , which are identical or different, represent a heteroatom chosen from oxygen and sulphur, a group -C(O)-O- or -OC(O)-, a group -OC(O)-O- or -OC(O) -O-; preferably X _a represents an oxygen atom;

X ¹ , AndX ² , identical or different, representing a heteroatom chosen from oxygen, sulfur and amino N(R'') with R'' being a hydrogen atom or a group (C₁-VS₆) alkyl, linear or branched; preferably x¹and X²represent an oxygen atom; (VS) (D) (E) (F) Formulas(VS),(D),(E)Or(F)in which :

• R represents a group chosen from:

i) (C₁-VS₁₀) alkyl, optionally substituted, preferably by one or more atoms or groups chosen from halogen, hydroxy, (C₁-VS₁₀)alkoxy, (hetero)cycloalkyl comprising between 5 and 10 members such as morpholinyl, and amino R_ToR_bN- with R_To, R_b, identical or different, representing a hydrogen atom or a group (C₁-VS₁₀)alkyl or R_Toand R_bform together with the nitrogen atom which bears them a heteroaryl or heterocycloalkyl group such as morpholino;
ii) (C₁-VS₁₀)alkoxy optionally substituted, preferably by the same substituents as for i) (C₁-VS₁₀)alkyl;
iii) hydroxy;
iv) optionally substituted (hetero)aryl such as optionally substituted phenyl of formula(VS')
withR' ¹ , R' ² , R' ³ ,identical or different, being as defined forR ¹ ,R ² ,R ³ And
representing the point of attachment to the rest of the molecule;
v) (hetero)cycloalkyl optionally substituted preferably by a hydroxy group or a group (C₁-VS₁₀)alkyl;
(vi) R⁴-(X)_not-C(X)-(X)_not'- with R⁴representing a group (C₁-VS₁₀) optionally substituted alkyl, optionally substituted (hetero)aryl such as optionally substituted phenyl of formula(VS'), optionally substituted (hetero)cycloalkyl, n and n', identical or different, being 0 or 1;
vii) R_vsR_dP(X)- with R_vsrepresenting a group (C₁-VS₁₀)optionally substituted alkyl, or (hetero)aryl optionally substituted, and R_drepresenting an optionally substituted (hetero)aryl group;
viii) or else R¹with R in ortho of the group C(X)-R or R'' and R''¹in ortho of the R’-Y group⁺-R'' form together with the atoms which carry them a (hetero)cycle fused to the phenyl or (hetero)aryl fused to the phenyl optionally substituted in particular on the non-aromatic part by one or more oxo or thiooxo groups; preferably R¹with R ortho to the group C(X)-R form together with the atoms which carry them and the fused phenyl ring an anthraquinone group(G): (G)

• R ¹ ,R ² OrR ³ , identical or different, represent a i) hydrogen atom, ii) of halogen such as chlorine, iii) a group (C₁-VS₁₀) optionally substituted alkyl, iv) (C₁-VS₁₀)alkoxy optionally substituted in particular by a hydroxy group, v) (hetero)aryl optionally substituted, vi) (hetero)cycloalkyl optionally substituted, vii) carboxy, viii) cyano, ix) nitro, x) nitroso, xi) -S(O )_p-OM with p equal to 1 or 2, M representing a hydrogen atom, an alkali or alkaline-earth metal, xii) R⁴R⁵NOT- ; xiii) R⁴-(X)_not-C(X)-(X)_not'- with R⁴, n and n’ as previously defined, R⁵is as defined for R⁴or else R⁴and R⁵form together with the nitrogen atom which carries them an optionally substituted heterocycloalkyl or heteroaryl such as morpholino, identical or different, being 0 or 1, xiv) hydroxy, or xv) thiol;
• R'' ¹ , R'' ² or R'' ³ , identical or different, are as defined for R ¹ , R ² , R ³ , preferably are chosen from the hydrogen atom or R ⁴ -Y– with R ⁴ being as defined previously and preferably a phenyl group;
• orRAndR ¹ contiguous,form together with the carbon atoms which bear them an optionally unsaturated and optionally substituted (hetero)cycloalkyl group, preferably cycloalkyl optionally substituted and in particular by one or more oxo groups and/or optionally fused by an aryl group such as benzo;
• or two substituents contiguousR ¹ ,R ² and orR' ¹ ,R' ² together form a group derived from maleic anhydride such as –C(X)-X-C(X)–;
• X , which is identical or different, represents an oxygen or sulfur atom or an NR ⁵ group with R ⁵ as defined previously, preferably representing a hydrogen atom or a (C ₁ -C ₁₀ )alkyl group; more particularly X represents an oxygen atom;
• Y is as defined for X , preferably Y represents a sulfur atom;
• Metal represents a transition metal such as iron or chromium, preferably Fe, said metal possibly being cationic in which case the initiator of formula (D) comprises a number of anionic counter-ion An ^- as defined previously, making it possible to achieve the electroneutrality of the molecule;
• IAndI', identical or different, representing a transition metal ligand preferably chosen from the following electron donors C(X) with X as defined above, cyano CN, (C₁-VS₆)alkenyl, optionally substituted (hetero)aryl such as bipyridinyl, amines such as amines R⁴R⁵R⁶N with R⁴and R⁵as previously defined and R⁶representing a hydrogen atom, or a group as defined for R⁴, phosphine R⁴R⁵R⁶P such as tri(hetero)arylphosphine, (hetero)cycloalkyl preferably being unsaturated such as cyclopentadiene, carbene such as arduengo carbene,
• q representing an integer comprised inclusively between 1 and 6, making it possible to achieve the stability of the metal complex, i.e. so as to obtain a number of electrons around the Metal equal to 16 or 18 electrons (one also speaks of a coordination sphere with 16 or 18 electrons), ;
• R' and R'', identical or different, represent an optionally substituted (hetero)aryl group;
• An ⁻ represents an anionic counter ion as defined previously preferably chosen from (Hal) ₆ P ^−, or (Hal) ₆ Sb ^−, with Hal, identical or different, representing a halogen atom such as fluorine; And
• R ^a , R ^b , R ^c or R ^d , which are identical or different, represent a hydrogen atom or a (C ₁ -C ₁₀ )alkyl group.

We can also cite as radical initiators ix) photoactive coloring compounds called " photosensitizing dyes " such as ethyl eosin, eosin Y, fluorescein, rose bengal, methylene blue, erythrosine, phloxime, thionine , riboflavin, and methylene green.
According to a particular embodiment of the invention, a combination of initiator compounds is used.

According to a particularly advantageous embodiment of the invention, the free radical initiator(s) ix) useful for the polymerization are of formula (A) or (B) as defined previously. More particularly, the radical initiator(s) ix) are of formula (A) .

According to another particular embodiment of the invention, the radical initiator(s) ix) useful for the polymerization are of formula(B)as defined above, preferably with Xa representing a group O, R with R₁and R' with R₃form together with the carbon atom which bears them an oxo group and R₂ and R₄, represent a groupR ₅ -(O) _w -where w is 1, R₅representing an optionally substituted (hetero)aryl group such as phenyl or an optionally substituted (hetero)cycloalkyl group in particular by a group (C₁-VS₆)alkyl such as cyclohexyl optionally substituted by a group (C₁-VS₆)alkyl.
According to another embodiment, the radical initiator(s) ix) useful for the polymerization are of formula(B)as defined above, preferably with Xa representing an oxygen atom,R ₁ ,R ₂ ,R ₃ , AndR ₄ , identical or different, represent a hydrogen atom or a group (C₁-VS₈) alkyl, linear or preferably linear branched such as methyl, ethyl, n-butyl andR, AndR'identical or different represent a radical (C₁-VS₈) alkyl, linear or branched, preferably linear,

According to a particular embodiment of the invention, the radical initiator ix) is AIBN (azo-bisisobutyronitrile). This initiator or initiator generates free radicals i) under the influence of heat at a temperature greater than or equal to 45°C, preferably at a temperature greater than or equal to 55°C more particularly at 60°C; and/or ii) photochemically.

According to another particular embodiment of the invention, the radical initiator ix) is ABDV (2,2'-azo-bis-(2,4-dimethylvaleronitrile)). The latter allows it to be used under thermally “softer” polymerization conditions.

Preferably when ABDV is used, the polymerization process is carried out at a temperature greater than or equal to 28°C, preferably at a temperature greater than or equal to 35°C, such as 40°C.

As initiators that can be used in the context of the present invention, mention may also be made of alkali metal or alkaline earth metal persulfates such as potassium persulfate.

The polymerization is preferentially carried out in the presence of initiators ix) chosen from peroxide initiators, azo initiators, oxidation-reduction (redox) couples, and photochemical initiators.

Mention may in particular be made more preferably of the initiators ix) chosen from:
- peroxides in particular chosen from tert-Butyl peroxy-2-ethylhexanoate: Trigonox 21S; 2,5-dimethyl-2,5-di(2-ethylhexanoylperoxy)hexane: Trigonox 141; tert-butyl peroxypivalate: Trigonox 25C75 from AkzoNobel, or alkali or alkaline earth metal persulfate such as potassium persulfate (KPS); Or
- azo compounds in particular chosen from AIBN: azobisisobutyronitrile; V50: 2,2'-azo-bis(2-amidinopropane) dihydrohalide such as dihydrochloride.
Preferably the polymerization is carried out at a temperature between 40°C and 110°C, more particularly between 60°C and 100°C such as 90°C.

Preparation method of dispersion (A) and material (C)

Without this being limiting, in general, the dispersion according to the invention can be prepared in the following way:
- The polymerization is carried out in " dispersion " by precipitation of the polymer particles i) during formation, with protection of the particles formed with one or more stabilizing agents ii) as defined previously, preferably a single type of stabilizing agent ii) chosen from d) and e) as defined previously.
According to one embodiment of the invention, the method of the invention comprises the following successive steps:
- In a ^1st step:
the stabilizing polymer (or stabilizing agent ii)) is prepared by mixing the monomer or monomers constituting the stabilizing polymer d), or e) as defined previously with one or more radical initiators ix), in a medium called synthesis medium, and by polymerizing these monomers, the synthesis medium preferably comprises iii) one or more liquid fatty substance(s) as defined above; then, to the stabilizing polymer ii) thus formed, the monomers constituting a first family of particles i) are added, in particular the monomers a ₁ ) and/or a ₂ ), and a ₃ ), preferably a ₁ ) and a ₃ ), plus preferably a''' ₁ ) and a ₃ ) as defined previously, and the polymerization of these monomers is carried out by the presence of radical initiator(s) ix); Then
- In a ^2nd step, a composition (B) containing:
A ) monomers such as:
A1) a mixture of monomers (M) containing:
- monomers a ₁ ) as defined previously, preferably (C ₁ -C ₄ )(alkyl)acrylate of (C ₁ -C ₄ )alkyl whose group(s) (C ₁ -C ₄ )alkyl are substituted by a hydroxy such as the monomers of formula (I′) as defined above, more preferably 2-hydroxyethyl acrylate;
- and/or monomers a ₂ ) as defined previously and
- monomers a ₃ ) as defined previously, preferably of formula (5) such as (meth)acrylic acids, preferably acrylic acid;
said mixture (M) preferably containing only monomers a ₁ ) and a ₃ );
Or
A2) monomers a ₃ ) as defined above, preferably of formula (5) and more particularly acrylic acid;
said composition (B) additionally containing
B ) one or more radical initiators ix) in particular alkali metal or alkaline earth metal persulfate(s) such as potassium persulfate,
C) optionally one or more polyols iv) liquid(s) at 20°C and 1 atmosphere as defined above, preferably chosen from (C ₂ -C ₆ )alkane-diol and (C ₂ - C ₆ )alkane-triol such as glycerol and/or water v),
D) optionally one or more crosslinkers vii) as defined above, chosen in particular from (VII ₆ ) , (VII' ₆ ), (VII ₇ ) and (VII ₈ ), such as Ethylene Glycol Diacrylate, Tetra(ethylene glycol) diacrylate , and diethylene glycol diacrylate (DEGDA), preferably DEGDA ,
E) optionally one or more neutralizers viii) chosen in particular from organic or inorganic alkaline agents, preferably inorganic such as sodium hydroxide or potassium hydroxide,
possibly water v),
it being understood that composition (B) contains C) and/or water v), this composition (B) is added to the medium obtained in the preceding step, the polymerization of these monomers being preferably carried out with stirring and preferably with heating for a duration comprised particularly between 1 minute and 1 day, more particularly between 30 minutes and 10 hours, such as 7 h at a temperature below 100° C. and above 70° C. such as 90° C.; then the medium is left to return to room temperature; Then
optionally when the composition (B) does not contain polyol is added during the ^1st step or during a ^3rd step in the middle one or more polyol (s) liquid (s) at 20 ° C and 1 atmosphere iv) as defined above, preferably chosen from (C ₂ -C ₆ )alkane-diol and (C ₂ -C ₆ )alkane-triol such as glycerol.
It is therefore understood that said process comprises at least one step implementing at least one polyol iv) as defined previously, either in the ^1st step, or in the ^2nd step, or in the ^3rd step.

According to one embodiment, composition (B) preferably comprises A + B + D and optionally C and/or E and water v);
According to a particular embodiment, composition (B) comprises: A + B + C + D + E and water v).
According to a particular embodiment, composition (B) comprises A + B + C + D + E and does not contain water v).

In particular, the synthesis medium of the ^1st stage is apolar and volatile organic preferably chosen from alkanes such as heptane, cyclohexane, Cetiol UT or the mixture of C ₉ -C ₁₂ alkanes, preferably of natural origin, in particular linear or branched C ₉ -C ₁₂ alkanes. This latter mixture is in particular known under the INCI name C ₉ -C ₁₂ ALCANE E511470, CAS 68608-12-8, VEGELIGHT SILK® marketed by BioSynthIs, or isododecane, preferably isododecane;
or a mixture of:
- an apolar solvent as defined above, in particular isododecane;
- a polar solvent chosen in particular from esters such as (C ₁ -C ₄ ) alkoxide (C ₁ -C ₄ ) alkyl, for example ethyl acetate;
when the synthesis of the ^1st step is complete, the additional solvent is removed and a mixture i) and ii) is obtained in the liquid fatty substance;
When the synthesis medium of stage 1 is a liquid hydrocarbon-based fatty substance iii) volatile, the polymerization can be carried out directly in said oil which therefore also acts as a synthesis solvent.
According to a particular form of the invention, the synthesis medium of the ^1st stage is a mixture of liquid fatty substances such as iii) and in particular isododecane with an additional solvent chosen in particular from esters with a hydrocarbon or branched aliphatic chain, having from 3 to 8 carbon atoms in total, such as ethyl acetate, methyl acetate, propyl acetate, n-butyl acetate and in particular ethyl acetate, said additional solvent being chosen to have a boiling point lower than that of the liquid fatty substance. When the synthesis of the stabilizers ii) and of the particles i) of step 1 is complete, the additional solvent is removed and a mixture i) and ii) is obtained in the liquid fatty substance.
The monomers are preferably present in the synthesis medium of the ^1st stage, before polymerization, in a proportion of 15% to 45% by weight. All of the monomers can be present in the solvent before the start of the reaction, or part of the monomers can be added as the polymerization reaction progresses.
The polymerization is preferably carried out at a temperature ranging from 70° C. to 110° C. and at atmospheric pressure.
In the event of the presence of cosmetic active ingredient(s) vi) chosen from f) to j) as defined above in dispersion (A), it(s) may be added during the first stage; according to another variant, the said cosmetic active ingredient(s) vi) is (are) added during the ^2nd stage or after the ^2nd stage; according to another variant, the said cosmetic active agent(s) vi) is (are) added during the 3 ^rd step or after the 3 ^rd step, preferably during the 3 ^rd step; if the active agent(s) are soluble in water, they are preferably found in composition (B) if said composition (B) as defined above contains water v).
According to one embodiment, composition (B) contains A1) a mixture of monomers (M) containing:
- monomers a ₁ ) as defined previously, preferably (C ₁ -C ₄ )(alkyl)acrylate of (C ₁ -C ₄ )alkyl whose group(s) (C ₁ -C ₄ )alkyl are substituted by a hydroxy such as the monomers of formula (I′) as defined above, more preferably 2-hydroxyethyl acrylate;
- and/or monomers a ₂ ) as defined previously
- and monomers a ₃ ) as defined above, preferably of formula (5) such as (meth)acrylic acids, preferably acrylic acid;
said mixture (M) preferably containing only monomers a ₁ ), preferably chosen from the monomers of formula (I′), more preferably 2-hydroxyethyl(meth)acrylate, and monomers a ₃ ) preferably chosen from the monomers of formula (I′) more preferably acrylic acid.
According to one embodiment, composition (B) contains A2) monomers a ₃ ) as defined above, preferably of formula (5) and more particularly acrylic acid.

The stabilizer ii) is preferably present in the mixture before polymerization of the monomers of the polymer of the particles i). However, it is also possible to add it continuously, in particular when the monomers of the particles i) are also continuously added.

It is possible to use from 0.1% to 50% by weight, particularly from 0.3 to 30% by weight, more particularly from 0.5% to 10% by weight of the stabilizing agent(s) relative to the total weight of monomers put implemented (stabilizing agents ii) + polymer particles i)), and preferably from 0.9% to 6.3% by weight, relative to the total weight of monomers used.

The dispersion of polymer particles (A) advantageously comprises from 8% to 40% by weight of dry matter, relative to the total weight of said dispersion, and preferably from 15% to 30% by weight relative to the total weight of said dispersion.

The composition according to the invention preferably comprises a content of dry matter (or active ingredient) of particle polymers i) + dispersant polymers ii) ranging from 5% to 60% by weight, relative to the total weight of the dispersion (A ), and preferably ranging from 8% to 40% by weight, in particular 15% to 30% by weight, relative to the total weight of the dispersion (A).

In a particular method of preparation, the random stabilizing polymer ii) is prepared in a first step. This stabilizing polymer is soluble in an apolar organic solvent of the alkane type such as isododecane.

Then, the at least two particles of different chemical composition i) are synthesized sequentially in the presence of the stabilizing polymer ii).

The stabilizing polymer ii) can be prepared by radical polymerization optionally in the presence of polymerization initiator vi) as defined previously.

According to one form of the invention, the particles i1) resulting from the polymerization of monomers a ₁ ) and/or a ₂ ), and a ₃ ), preferably a ₁ ) and a ₃ ), more preferably a''' ₁ ) and a ₃ ) in the first stage, then the particles i2) resulting from the polymerization of a mixture of monomers a ₁ ) and/or a ₂ ), and a ₃ ) different from that used are prepared. work for i1), or of monomers a ₃ ) as defined previously.

The dispersions (A) according to the invention are therefore ultimately formed of polymeric particles, of fairly large diameter (preferably greater than 50 nm), and will lead to film-forming deposits, and resistant to fatty substances at the observation temperature. (25°C).

In addition, said dispersion being in an oily medium and possibly containing water v), it becomes easy to formulate it in cosmetic compositions based on an oily medium commonly used in cosmetics, in particular in the fatty phases of emulsions, but also in the aqueous phases of emulsions to make it possible to solubilize the water-soluble or hydrophilic active agents.

According to a particular embodiment of the invention, the method is carried out according to the following 3 steps:

For the preparation of these new dispersions, the following process can also be implemented:

The polymeric material (C)

A subject of the invention is also a polymeric material (C), obtained by evaporation of the water v) - if present in the medium - and of the liquid fatty substance(s) iii) of the dispersion (A) as defined above.

According to a particular embodiment of the invention, the material (C) comprises one or more polyol(s) in an amount greater than or equal to 5% by weight and less than 95% by weight relative to the total weight of the material, particularly the amount of polyol(s) is between 10% and 90% by weight relative to the total weight of the material, more particularly between 20% and 85% by weight, more particularly between 30% and 80% by weight, relative to the total material weight (C).

Process for treating keratin materials from the dispersion (A):

According to an advantageous variant of the invention, the process of the invention is a process for the treatment of keratinous fibres, in particular human, preferably the hair, which implements the application to said fibers of at least one dispersion (A) such than previously defined.

According to a particular embodiment of the invention, the process for treating keratin materials is a treatment of the skin and/or the eyelashes, eyebrows implementing the application to the skin and/or the eyelashes, eyebrows the dispersion (A ) as defined above, followed by a step of drying in the open air or else dried using conventional devices used in cosmetics such as a hair dryer or a heating lamp, preferably in the open air.

According to a particular embodiment of the invention, the process for treating keratin materials is a process for making up the skin and/or the eyelashes, eyebrows implementing a step of applying the dispersion (A) optionally comprising at least one cosmetic active vi) chosen from ingredients f) to j) as defined previously, in particular chosen from pigments g), and active ingredients for the skin h) in particular moisturizers different from iv) and/or antioxidants, preferably moisturizers, and optionally comprising at least one neutralizer viii) as defined previously.

The dispersion (A) according to the invention or the compositions, in particular cosmetic compositions containing it, may also comprise a cosmetic additive chosen from perfumes, preservatives, fillers, waxes, vitamins, ceramides, polymers other than i) and ii) and thickeners.

Preferably, the process for treating keratin materials of the invention comprises the application of the dispersion (A) to the keratin materials, followed by drying in the open air.

According to an advantageous variant, the polymeric material (C) is obtained directly on the substrate, in particular on the keratin materials, in particular the skin once the water, the solvent or solvents, and liquid fatty substances of the dispersion (A). , evaporated in the open air or using a suitable device such as a device promoting evaporation by an influx of air and/or heat such as a hair dryer,

According to an advantageous variant, the dispersion (A) once applied to the keratin materials, in particular the skin, is left to dry for at least 30 seconds, particularly between 1 minute and 30 minutes, more particularly between 5 minutes and 10 minutes.

According to another advantageous variant, the dispersion (A) is applied using a spatula, in particular without stirring the dispersion beforehand, until the surface is filled and flattened with said spatula, the excess is mechanically removed using said spatula, followed by a drying step or left to dry in the open air as defined above.

According to a particular embodiment of the invention, the method implements an additional step of removing the polymeric material (C) by scraping, in particular with the fingernail of one hand, the surface of the part treated with the dispersion (A) during the 1 ^st or 2 ^nd stage, then by removing said polymeric material (C) like a film between the thumb and the index finger.

The dispersion (A) according to the invention finds an application for the care of the skin and/or the lips.

The invention is further illustrated in the following examples.
EXAMPLES

The dispersions (A) of examples 1 to 6 (invention) were produced in 2 stages, the first stage being that of the process for preparing example 4 of international application WO 2015/091513.

Step 1 : Preparation of the oily dispersion comprising particles i) and stabilizer ii) prepared from Acrylic Acid, Methyl Acrylate, Ethyl Acrylate, and Isobornyl Acrylate in the isododecane.

The oily dispersions (step 1 of table 1) used in examples 1 to 6, and 1' to 6' below were produced according to the method of preparation of example 4 of international application WO 2015/091513 by putting uses the following raw materials:
For the synthesis of the stabilizer ii): Reagents Mass (g) Isobornyl Acrylate 315.2 Methyl Acrylate 12.5 Ethyl Acrylate 12.5 Trigonox 21S 3.4 Isododecane / AcOEt (60/40) 900

At the end of the synthesis of the stabilizer, the medium is diluted with 900 g of an isododecane/ethyl acetate mixture 60/40 by weight.

For the synthesis of particles i): Reagents Mass (g) Methyl Acrylate 145 Ethyl Acrylate 934 Acrylic Acid 157 Trigonox 21S 12.36 Isododecane / AcOEt (60/40) 1236

At the end of the synthesis, a stripping of 3L of isododecane is then carried out to eliminate the ethyl acetate.

A dispersion is thus prepared containing particles i1) at 10% by weight of Acrylic Acid, 10% by weight of Methyl Acrylate, 60% by weight of Ethyl Acrylate and 20% by weight of Acrylate d 'Isobornyl in isododecane.

The dry extract is about 50% w.
The mass ratio between the particles and the Stab
2nd step :

Preparation of composition B) for the preparation of particles i2)

Sodium hydroxide in the form of pellets is dissolved in water with magnetic stirring (250 rpm). The reaction is exothermic and is controlled using an ice bath.

The monomer(s) are then added little by little with stirring while cooling.

Finally, the polymerization initiator and the crosslinker, if any, are introduced. The mixture is homogenized with the SPEED MIXER 3500 RPM for 2 minutes twice.
A total of 6 aqueous compositions B1, B2, B3, B4, B5 and B6 were prepared. Reagents Aqueous phase B1 Aqueous phase B2 Aqueous phase B3 Aqueous phase B4 Aqueous phase B5 Aqueous phase B6 Acrylic acid 29.41 19.35 10.05 2.00 10.3 29.67 2-Hydroxyethyl acrylate - - 10.05 18.00 10.3 - Sodium hydroxide 12.25 9.18 4.26 0.83 4.29 12.36 Di ethylene glycol diacrylate (DEGDA) 0.88 2.58 2.18 1.76 - - Potassium Persulfate (KPS) 1.1 0.74 0.61 0.49 0.63 1.11 Neutralization molar % / acrylic acid 75 85 75 75 75 75 Molar % crosslinking / monomer(s) 1.0 4.5 4.5 4.5 4.5 1.0 %molar Initiator / monomer(s) 1.0 1.0 1.0 1.0 1.0 1.0 Water Qsp 100 Qsp 100 Qsp 100 Qsp 100 Qsp 100 Qsp 100 Data in g per 100 g of composition unless otherwise indicated (% by weight)

Addition of composition (B) to the dispersion obtained in step 1

Phases B1 to B6 are added to the dispersion obtained in stage 1 at a rate of 60% by weight for 40% by weight of dispersion obtained in stage 1, with stirring at ambient temperature (25° C.). The stirred mixture obtained is heated for a period of several hours (approximately 7 h) at 90°C. The medium is left to return to room temperature.

Step 3 : Addition of polyol

For Examples 1 to 6, the polyol (glycerol) is added to the medium obtained in step 2 according to the amounts indicated below; the tests correspond to a quantity of polyol (glycerol) of 70% by weight once the film is dry.

Example 1 2 3 4 5 6 % by weight of polyol (glycerol) added to the mixture obtained in step 2
50.1 46.1 45.1 44 44.4 49.9

For the compositions of examples 1′ to 6′ (outside the invention), an equivalent quantity of water is added (instead of the polyol).

The mass composition of each of examples 1 to 6 of dispersions (A) is as follows: Preparation steps Ingredients Ex 1 Ex 2 Ex 3 Ex 4 Ex 5 Ex 6 Step 1 Preparation of the oily dispersion Isobornyl acrylate 1.9 2.1 2.1 2.2 2.1 1.9 Methyl acrylate 1.0 1.1 1.1 1.1 1.1 1.0 Ethyl acrylate 6.0 6.5 6.6 6.8 6.7 6.1 Acrylic acid 1.0 1.1 1, 1 1.1 1.1 1.0 Isododecane 10.0 10.8 11.0 11.2 11.1 10.0 2nd step
Preparation of the aqueous phase preparation B 2-hydroxyethyl acrylate - - 3.3 6.1 3.4 - Acrylic acid 8.8 6.2 3.3 0.7 3.4 8.9 Sodium hydroxide 3.7 3.0 1.4 0.3 1.4 3.7 Potassium persulfate 0.3 0.2 0.2 0.2 0.2 0.3 Di(ethylene glycol) diacrylate 0.3 0.8 0.7 0.6 - - Water 16.9 22.0 24.0 25.9 24.8 17.1 Step 3
Addition of polyol Glycerol 50.1 46.1 45.1 44.0 44.4 49.9 The mass composition of each of the comparative examples 1′ to 6′ (outside the invention) is as follows: Preparation steps Ingredients Ex 1' Ex 2' Ex 3' Ex 4' Ex 5' Ex 6' Step 1 Preparation of the oily dispersion Isobornyl acrylate 1.9 2.1 2.1 2.2 2.1 1.9 Methyl acrylate 1.0 1.1 1.1 1.1 1.1 1.0 Ethyl acrylate 6.0 6.5 6.6 6.8 6.7 6.1 Acrylic acid 1.0 1.1 1, 1 1.1 1.1 1.0 Isododecane 10.0 10.8 11.0 11.2 11.1 10.0 2nd step
Preparation of the aqueous phase preparation B 2-hydroxyethyl acrylate - - 3.3 6.1 3.4 - Acrylic acid 8.8 6.2 3.3 0.7 3.4 8.9 Sodium hydroxide 3.7 3.0 1.4 0.3 1.4 3.7 Potassium persulfate 0.3 0.2 0.2 0.2 0.2 0.3 Di(ethylene glycol) diacrylate 0.3 0.8 0.7 0.6 - - Water 16.9 22.0 24.0 25.9 24.8 17.1 Step 3
Adding water Water 50.1 46.1 45.1 44.0 44.4 49.9

The dispersions (A) according to the invention of compositions B1 to B6 and the dispersions outside the invention of B′1 to B′6 are then applied to a substrate.
The chosen substrate is Bioskin® (reference K520 bioskin plate # 10-04-smooth and flight surf thickness 2 mm). On the latter, an incision is made using a scalpel to create an artificial wrinkle. A wet film of each of the compositions 1 to 6, respectively 1' to 6', and 100 μm is deposited on the support with a film puller. It is left to air dry at room temperature for at least 12 hours and the thickness of the film is measured by OCT (optical coherence tomography Ganymede from Thorlabs) at the place where the incision (wrinkle) is the deepest (according to the z-axis).

The results are in Table 7.

Examples
Invention with polyol
Film removal* Comparative examples without polyol
Film removal*
1

11%

1'
78%

2
19%
2' 78%
3
18%
3' 83%
4
25%
4' 78%
5
16%
5' 80%
6
13%
6' 78% * relative to the deepest part of the incision.

It was observed from the loss measurements with respect to the Z axis that there is an average shrinkage of 20% of the film at the surface of the incision for compositions 1 to 6 of the invention comprising a polyol such as glycerol against 80% for the compositions outside the invention 1′ to 6′ in which the polyol has been substituted with water. Significant and lasting filling of the incision by the compositions of Examples 1 to 6 is thus observed.

Claims (22)

Dispersion (A), which includes:
i) at least two particle(s) of different chemical structures consisting of polymer(s) obtained by polymerization of monomers chosen from ethylenic monomers of:
a ₁ ) (C ₁ -C ₄ )(alkyl)acrylate (C ₁ -C ₄ )alkyl whose (C ₁ -C ₄ )alkyl group(s) are optionally substituted by one or more group(s) chosen from hydroxy , and (di)(C ₁ -C ₄ )(alkyl)amino ,
a ₂ ) poly[oxy(C ₁ -C ₄ )alkylene] (C ₁ -C ₄ )(alkyl)acrylate,
a ₃ ) ethylenic monomers comprising one or more groups chosen from carboxy, anhydride, phosphoric acid, and sulphonic acid;
it being understood that each particle results from the polymerization of one or more ethylenic monomer(s) a ₃ ); And
ii) one or more polymeric stabilizing agent(s) chosen from:
d) ethylenic polymers of monomers of (C ₁ -C ₆ )(alkyl)acrylate of (C ₃ -C ₁₂ )cycloalkyl, preferably ethylenic homopolymers of (C ₁ -C ₆ )(alkyl)acrylate of (C ₃ -C ₁₂ )cycloalkyl, more preferentially the ethylenic homopolymers of (meth)acrylate of (C ₃ -C ₁₂ )cycloalkyl; And
e) copolymers of ethylenic monomers of:
e ₁ ) (C ₁ -C ₆ )(alkyl)acrylate (C ₃ -C ₁₂ )cycloalkyl, and
e ₂ ) (C ₁ -C ₄ )(alkyl)acrylate of (C ₁ -C ₄ )alkyl, preferably copolymers of (meth)acrylate of (C ₃ -C ₁₂ )cycloalkyl and (meth)acrylate of (C ₁ -C ₄ )alkyl; And
iii) one or more liquid fat(s) at 20°C and 1 atmosphere, preferably volatile hydrocarbon(s); And
iv) one or more polyol(s) liquid(s) at 20°C and 1 atmosphere; And
v) optionally water; And
vi) optionally one or more cosmetic active ingredient(s) different from iii) and from iv), chosen from f) dyes, g) pigments; h) active ingredients for the care of keratin materials, in particular the skin, in particular antioxidants and moisturizers other than iv), i) UV filters (A) and/or (B), or j) mixtures of f) to i). Dispersion (A), according to the preceding claim, which comprises at least one particle i1) consisting of copolymer derived from monomers a ₁ ) and/or a ₂ ) and a ₃ ) and at least one particle i2) of chemical composition different from i1) chosen from a copolymer derived from monomers a ₁ ) and/or a ₂ ) and a ₃ ), a copolymer derived from monomers a ₃ ), a homopolymer derived from monomers a ₃ ). Dispersion (A), according to any one of the preceding claims, which comprises at least two particle(s) of different chemical structures i) containing the particles A1 consisting of copolymers of ethylenic monomers:
a ₁ ) (C ₁ -C ₄ )(alkyl)acrylate of (C ₁ -C ₄ )alkyl whose (C ₁ -C ₄ )alkyl group(s) are optionally substituted by one or more groups chosen from hydroxy, (di )((C ₁ -C ₄ )alkyl)amino; and or
a ₂ ) poly[oxy(C ₁ -C ₄ )alkylene] (C ₁ -C ₄ )(alkyl)acrylate, and
a ₃ ) ethylenic monomers comprising one or more carboxy, anhydride, phosphoric acid, sulphonic acid groups,
preferably consisting of copolymers of ethylenic monomers a ₁ ) and a ₃ ), or a ₂ ) and a ₃ ), more preferably a ₁ ) and a ₃ ). Dispersion (A), according to any one of the preceding claims, which comprises at least two particle(s) of different chemical structures i) containing particles A'1 consisting of copolymers of ethylenic monomers a' ₁ )(C ₁ -C ₄ )( (C ₁ -C ₄ )alkyl alkyl)acrylate and a ₃ ) ethylenic monomers comprising one or more carboxy, anhydride, phosphoric acid, sulfonic acid, and/or
containing particles A'2 consisting of copolymers of ethylenic monomers a'' ₁ ) (C ₁ -C ₄ )(alkyl)acrylate of (C ₁ -C ₄ )alkyl substituted by one or more groups chosen from hydroxy, (di) ((C ₁ -C ₄ )alkyl)amino, preferably substituted by a hydroxy group such as 2-hydroxyethylacrylate (HEA) and a ₃ ) ethylenic monomers comprising one or more carboxy, anhydride, phosphoric acid or sulphonic acid groups;
preferably, the particles i) of the dispersion (A) and more preferably the particles i) of the dispersion (A) are a mixture of particles A'1 and A'2 , in particular in a mass ratio (mass of particles A '1 / mass of particles A'2 ) between 0.3 and 3, more particularly between 0.5 and 2.8, even more preferably between 0.6 and 2. Dispersion (A), according to any one of the preceding claims, in which the polymer(s) constituting the particles i) is (are) chosen from ethylenic copolymers resulting from the polymerization of monomer of formula (I) with ethylenic monomers comprising one or more carboxy, anhydride, phosphoric acid, sulphonic acid groups a ₃ ):
H ₂ C=C(R)-C(O)-O-R' (I)
Formula (I) in which:
- R representing a hydrogen atom or a (C ₁ -C ₄ )alkyl group such as methyl, and
- R' representing a (C ₁ -C ₄ )alkyl group such as methyl or ethyl,
preferably the compound(s) of formula (I) is (are) chosen from C ₁ -C ₄ alkyl (meth)acrylates such as methyl (meth)acrylate, (meth) ethyl acrylate, n-propyl (meth)acrylate, isopropyl (meth)acrylate, n-butyl (meth)acrylate, or tert-butyl (meth)acrylate; more preferably chosen from methyl (meth)acrylate, ethyl (meth)acrylate, even more preferably the compound(s) of formula (I) represent(s) a C ₁ -C ₄ alkyl acrylate such as methyl acrylate. Dispersion (A), according to any one of the claims, in which the ethylenic monomers a ₃ ) comprising one or more carboxy, anhydride, phosphoric acid or sulphonic acid groups are chosen from (1) , (2) , (3) , and ( 4) :
(1) R ¹ (R ² )C=C(R ³ )-Acid with R ¹ , R ² and R ³ representing a hydrogen atom or a CO ₂ H, H ₂ PO ₄ , or SO ₃ H group, and Acid representing a carboxy, phosphoric acid, sulphonic acid, preferably carboxy, group, more particularly (1) represents (5) H ₂ C=C(R)-C(O)-OH with R representing a hydrogen atom, or a (C ₁ -C ₄ ) alkyl group such as methyl;
(2) H ₂ C=C(R)-C(O)-N(R')-Alk-Acid with R and R', which are identical or different, represent a hydrogen atom, or a group (C ₁ -C ₄ ) alkyl; Alk represents a (C ₁ -C ₆ )alkylene group optionally substituted by at least one group chosen from Acid as defined previously and hydroxy; and Acid is as defined above, preferably carboxy or sulphonic acid;
(3) Ar-(R ^a )C=C(R ^b )-R ^c with R ^a , R ^b and R ^c , identical or different, representing a hydrogen atom or a (C ₁ -C ₄ )alkyl group , and Ar represents an aryl group, preferably benzyl, optionally substituted by at least one CO ₂ H, H ₂ PO ₄ or SO ₃ H acid group, preferably substituted by a CO ₂ H or SO ₃ H group,
(4) Maleic anhydride of formula (4a) and (4b):

Formulas (4b) and (4b) in which R _a , R _b and R _c , identical or different, representing a hydrogen atom or a (C ₁ -C ₄ )alkyl group, preferably R _a , R _b , and R _c represent a hydrogen atom; preferably an ethylenically unsaturated anhydride monomer of the invention is of formula (4b) and more preferably is maleic anhydride; And
more particularly b ₁ ) is chosen from (1) and (4) , in particular (1) and more particularly (5) . Dispersion (A), according to any one of the preceding claims, in which the polymer(s) constituting the particles i) and A'1 and/or b ₁ ) is an ethylenic acrylate copolymer resulting from the polymerization:
- at least one monomer a ₁ ) of formula (I) as defined in claim 6, preferably C ₁ -C ₄ alkyl acrylate such as methyl acrylate, ethyl acrylate; And
- at least one monomer a ₃ ) of formula (5) as well as its salts of organic or mineral bases such as alkali metals or alkaline-earth metals such as Na or K. Dispersion (A), according to any one of the preceding claims, in which the polymer(s) constituting the particles i) is (are) chosen from:
*ethylene copolymers(I'A)resulting from the polymerization:
- a1’’) of at least one monomer of formula(I')
H ₂ C=C(R)-C(O)-O-R''
Formula(I')in which :
-Rrepresenting a hydrogen atom or group (C₁-VS₄)alkyl such as methyl, and
-R''representing a group (C₁-VS₄)alkyl substituted by one or more hydroxy groups (preferably the alkyl group is substituted at the end of the chain by a hydroxy group), such as hydroxymethyl or 2-hydroxyethyl, preferably(I')represents (meth)acrylate hydroxy(C₁-VS₄)alkyl such as hydroxyethyl acrylate; And
- a3’’) of at least one monomer of formula(5)as defined in the preceding claim; or
*ethylene copolymers(I'B)resulting from the polymerization:
- a2’’) of at least one monomer of formula
(I') H ₂ C=C(R)-C(O)-O-[ALK-O] _p -R'
Formula(I'')in which :
-Rrepresenting a hydrogen atom or group (C₁-VS₄)alkyl such as methyl, and
-R'representing a group (C₁-VS₄) alkyl such as methyl or ethyl;
-ALKrepresents a group (C₁-VS₆) alkylene optionally substituted with at least one group chosen from Acid as defined above and hydroxy;
-prepresents an integer greater than or equal to 1, preferably less than or equal to 100; And
- a3’’) of at least one monomer of formula(5)as previously defined; or
*ethylene copolymers(I'C)resulting from the polymerization:
- To'''₁) of monomers (C₁-VS₄(C) )(alkyl)acrylate₁-VS₄) alkyl preferably of formula(I)previously defined and or
- To₂) of monomers (C₁-VS₄poly[oxy(C)(alkyl)acrylate₁-VS₄)alkylene], and
- To₃) of ethylenic monomers comprising one or more carboxy, anhydride, phosphoric acid, sulphonic acid groups, preferably chosen from (1),(2),(3), And(4)as defined in claim 7, more particularly of formula(5)as defined previously and even more preferentially acrylic acid. Dispersion (A), according to any one of the preceding claims, in which the stabilizing agent(s) ii), is (are) chosen from:
d) ethylenic polymers of monomers of (C ₁ -C ₆ )(alkyl)acrylate of (C ₃ -C ₁₂ )cycloalkyl, preferably ethylenic homopolymers of monomers of (C ₁ -C ₆ )(alkyl)acrylate of ( C ₃ -C ₁₂ )cycloalkyl, more preferably (C ₃ -C ₁₂ )cycloalkyl (meth)acrylate homopolymers; more particularly the ethylenic homopolymers resulting from the polymerization of monomers of formula:
H ₂ C=C(R)-C(O)-O-R''
with R representing a hydrogen atom or a (C ₁ -C ₄ )alkyl group such as methyl, and R'' representing a (C ₅ -C ₁₀ )cycloalkyl group such as norbornyl, or isobornyl, preferably isobornyl. Dispersion (A), according to any one of Claims 1 to 9, in which the stabilizing agent(s) ii), is (are) chosen from:
e) copolymers of ethylenic monomers of e ₁ ) (C ₁ -C ₆ )(alkyl) cycloalkyl acrylate (C ₃ -C ₁₂ ), and of e ₂ ) (C ₁ -C ₄ )(alkyl) acrylate (C ₁ -C ₄ )alkyl, preferably copolymers of (C ₃ -C ₁₂ )cycloalkyl (meth)acrylate and (C ₁ -C ₄ )alkyl (meth)acrylate; preferably chosen from ethylenic copolymers e) of monomers of formula (IV) and of monomers of formula (III) :
H ₂ C=C(R)-C(O)-O-R' (III) and H ₂ C=C(R)-C(O)-O-R'' (IV)
Formulas (III) and (IV) in which
- R , identical or different, representing a hydrogen atom or a (C ₁ -C ₄ )alkyl group such as methyl,
- identical or different R' representing a (C ₁ -C ₄ )alkyl group such as methyl or ethyl, and
- R'' representing a (C ₅ -C ₁₀ )cycloalkyl group such as norbornyl, or isobornyl, preferably isobornyl; preferably R'' represents a (C ₅ -C ₁₀ )cycloalkyl group such as norbornyl, or isobornyl, preferably isobornyl;
or
d) ethylenic copolymers chosen from copolymers of (C ₁ -C ₆ )(alkyl)acrylate (C ₃ -C ₁₂ )cycloalkyl monomers in particular of formula (IV) . Dispersion (A), according to any one of the preceding claims, in which the hydrocarbon-based liquid fatty substance(s) iii) is (are) chosen from:
hydrocarbons, in particular alkanes, oils of animal origin, oils of vegetable origin, glycerides or fluorinated oils of synthetic origin, fatty alcohols, fatty acid and/or fatty alcohol esters, silicones; in particular the liquid hydrocarbon fatty substance(s) are linear or branched hydrocarbon oils, which are volatile, chosen in particular from undecane, dodecane, isododecane, tridecane, their mixture of different, volatile oils preferably comprising isododecane in the mixture, or a mixture of undecane and tridecane or else a mixture of non-volatile oil(s) and volatile oil(s) preferably the mixture comprises as volatile oil the undecane, dodecane, isododecane, tridecane, more preferably isododecane, as a volatile and non-volatile oil mixture, mention may be made of the mixture of isododecane and isononyl isononanoate. Dispersion (A), according to any one of the preceding claims, in which the hydrocarbon-based liquid fatty substance(s) iii) is (are) chosen from:
non-polar oils, i.e. formed solely from carbon and hydrogen atoms, preferably the dispersion (A) comprises at least one non-polar hydrocarbon-based liquid fatty substance iii), preferably chosen from:
- linear or branched C ₈ -C ₃₀ alkanes, in particular C ₁₀ -C ₂₀ , more particularly C ₁₀ -C ₁₆ alkanes, volatile or non-volatile; preferably volatile
- cyclic, non-aromatic, C ₅ -C ₁₂ alkanes; volatile or non-volatile; preferably volatile, and
- their mixtures;
preferably iii) is (are) chosen from hydrocarbon oils having from 8 to 16 carbon atoms, in particular having from 10 to 14 carbon atoms, preferably volatile, more particularly the apolar oils, described above; among the branched C ₈ -C ₁₆ alkanes, in particular C ₁₀ -C ₁₄ suitable as liquid hydrocarbon fatty substances iii) in the dispersion, mention may be made of:
- isoalkanes of petroleum origin such as isododecane;
- linear alkanes, such as undecane (C ₁₁ ), n-dodecane (C ₁₂ ), n-tridecane (C ₁₃ ) and n-tetradecane (C ₁₄ ), as well as their mixtures, the undecane-tridecane mixture, mixtures of n-undecane (C ₁₁ ) and n-tridecane (C ₁₃ );
preferentially, the liquid hydrocarbon fatty substance(s) iii) are apolar, more particularly isododecane, or the liquid hydrocarbon fatty substance(s) iii) are a mixture of volatile oils or a mixture of one or more oil(s) non-volatile(s) and volatile oil(s) preferably the mixture comprises isododecane or a mixture of oils, in particular of undecane and tridecane as volatile oil and isononyl isononanoate and/or octyldodecanol as a non-volatile oil. Dispersion (A), according to any one of the preceding claims, in which the hydrocarbon liquid fatty substance(s) iii) is (are) present in the dispersion:
in an amount of between 1% and 25% by weight, more preferably between 2.5% and 20% by weight, even more preferably between 4% and 15% such as 10% by weight relative to the total weight of said dispersion ( A) with water v); or
in an amount of between 1.5% and 30% by weight, more preferably between 4% and 20% by weight, even more preferably between 8 and 15%, especially between 12% and 13% by weight relative to the total weight of said dispersion (A) free of water; in particular the ratio by weight of the sum of the ingredients [i) + ii)] / iii) is less than or equal to 3, more particularly [i) + ii]] / iii) the ratio by mass is between 1 and 2, 5, even more particularly is between 1.5 and 2.4, preferably between 1.7 and 2.2. Dispersion (A), according to any one of the preceding claims, in which the polyol(s) iv) has (have) a molecular weight of between 50 g/mol and 300 g/mol, more particularly between 80 g/mol and 150 g/mol;
preferably the polyol(s) iv) is (are) chosen from:
- (C ₂ -C ₆ )alkane-diol hydrocarbon compounds; And
- (C ₂ -C ₆ )alkane-triol such as glycerol and butane triols, and pentane triols, and hexane triols such as hexane-1,2,6-triol;
more preferably, the polyol(s) iv) is (are) chosen from hydrocarbon compounds (C ₂ -C ₆ )alkane-triols such as glycerol. Dispersion (A), according to any one of the preceding claims, in which comprising one or more crosslinking agent(s) iv), in particular chosen from the monomers of formula(V)And(VI)next : (V) (VI) Formulas(V)And(VI)in which :

• A represents an optionally substituted (hetero)aryl or optionally substituted (hetero)cycloalkyl group, preferably A represents a phenyl group;
• R ⁸ , identical or different, represents a hydrogen atom or a (C ₁ -C ₈ )alkyl group, linear or branched, optionally substituted, preferably C ₁ -C ₆ such as methyl;
• X ¹ AndX ² ,identical or different, represent a heteroatom chosen from oxygen, sulfur and amino N(R'') with R'' being a hydrogen atom or a group (C₁-VS₆)alkyl, linear or branched; preferably x¹= O or NH, and X²= O ; and more particularly X¹=X²= an oxygen atom, or elseX ¹ forms a bond;
• W represents: i) either a group A as defined above, in particular a 5- or 6-membered heteroaryl group such as pyridinyl or heterocycloalkyl comprising at least one 5- to 8-membered oxygen atom such as tetrahydrofuryl, piperazynyl or hexahydrofuro[ 3,2- b ]furanyl, ii) or a group *- A- (CR ⁹ R ¹⁰ ) _x -A-* when w is 2, with A as defined previously, R ⁹ and R ¹⁰ , identical or different representing a hydrogen atom or a (C ₁ -C ₆ )alkyl group such as methyl, preferably R ⁹ and R ¹⁰ = H, x represents an integer comprised inclusively between 0 and 10, preferably x = 1 and * represents the point of attachment to the -X ¹ -C(X ² )-C(=CH ₂ )-R ⁸ groups; iii) either a hydrocarbon chain, linear or branched, polyvalent, preferably di or trivalent, saturated or unsaturated, preferably saturated, optionally substituted, preferably by a hydroxy group, optionally interrupted by one or more heteroatoms such as O, and comprising 1 to 20 carbon atoms;
• p is 0 or 1;
• u and w represent an integer comprised inclusively between 2 and 10, more particularly between 2 and 5, such that u=2 and w=2 or 3;

preferably, the monomers of formula(V)And(VI)are chosen from the compounds in the following table, as well as their optical and geometric isomers, their tautomers and acid or base, inorganic or organic salts: Name Structure Styrene/divinyl benzene ( _V1 ) Diisopropyl benzene ( _V2 ) 1,3-phenylene diacrylamide;
1,4-phenylene diacrylamide (VI ₁ ) N , N'- 1,3-phenylenebis(2-methyl-2-propenamide);
N , N'- 1,4-phenylenebis(2-methyl-2-propenamide) (VI ₂ ) 3,5-bisacrylamido-benzoic acid with R'' identical and equal to H; and 3,5-bismethylacrylamido-benzoic acid with R'' identical and equal to CH ₃ (VI ₃ )
R'' = H or (C ₁ -C ₄ )alky such as CH ₃ 2,6-bisacryloyl-amidopyridine with R'' identical and equal to H;
2,6-bismethylacryloyl-amidopyridine with R'' identical and equal to CH ₃ (VI ₄ )
R'' = H or (C ₁ -C ₄ )alkyl such as CH ₃ 1,4-diacryloylpiperazine with R'' identical and equal to H; 1,4-dimethylacryloyl-piperazine with R'' identical and equal to CH ₃ (VI ₅ )
R'' = H or (C ₁ -C ₄ )alkyl such as CH ₃ Di Ethylene Glycol Di Acrylate (n=2)
Diethylene Glycol Di Methacrylate (n=2)
n is an integer greater than or equal to 1 and preferably between 1 and 10 and preferably between 2 and 4 and preferably 2

(VII ₆ )
R'' = H or (C ₁ -C ₄ )alkyl such as CH ₃ Ethylene glycol dimethacrylate with R'' identical and equal to CH ₃ (EGDMA); Ethylene glycol diacrylate with R'' identical and equal to H (VI ₆ )
R'' = H or (C ₁ -C ₄ ) such as CH ₃ Tetramethylene dimethacrylate with R'' identical and equal to CH ₃ ; Tetramethylene diacrylate with R'' identical and equal to H (VI ₇ )
R'' = H or (C ₁ -C ₄ )alkyl such as CH ₃ Hexamethylene dimethacrylate with R'' identical and equal to CH ₃ and Hexamethylene diacrylate with R'' identical and equal to H (VI ₈ )
R'' = H or (C ₁ -C ₄ )alkyl such as CH ₃ Anhydroerythritoldimethacrylate with R'' identical and equal to CH ₃ and Anhydroerythritoldiacrylate with R'' identical and equal to H (VI ₉ )
R'' = H or (C ₁ -C ₄ )alkyl such as CH ₃ 1,4;3,6-dianhydro-p-sorbitol-2,5-dimethacrylate with R'' identical and equal to CH ₃ ; 1,4;3,6-dianhydro-p-sorbitol-2,5-diacrylate with R'' identical and equal to H (VI ₁₀ )
R'' = H or (C ₁ -C ₄ )alkyl such as CH ₃ Isoproplenebis(1,4-phenylene)-dimethacrylate with R'' identical and equal to CH ₃ ; Isoproplenebis(1,4-phenylene)-diacrylate R'' identical and equal to H
(VI ₁₁ )
R'' = H or (C ₁ -C ₄ )alkyl such as CH ₃ 2,2-bis(Hydroxymethyl)butanol trimethacrylate with R'' identical and equal to CH ₃ (TRIM); 2,2-bis(Hydroxymethyl)butanol triacrylate R'' identical and equal to H
(VI ₁₂ )
R'' = H or (C ₁ -C ₄ )alkyl such as CH ₃ Pentaerythritol triacrylate with R'' identical and equal to H; Pentaerythritol trimethacrylate with R'' identical and equal to CH ₃ (VI ₁₃ )
R'' = H or (C ₁ -C ₄ )alkyl such as CH ₃ Pentaerythritol tetraacrylate with R'' identical and equal to H (PETRA); Pentaerythritol tetramethacrylate with R'' identical and equal to CH ₃ (VI ₁₄ )
R'' = H or (C ₁ -C ₄ )alkyl such as CH ₃ N,O -bismethacryloyl-ethanolamine with R _c equal to ethylene and R'' identical and equal to CH ₃
(VI ₁₅ )
R _c = (C ₁ -C ₆ )alkylene such as ethylene
R'' = H (C ₁ -C ₄ )alkyl such as CH ₃ N,N'- methylene-bis-acrylamide with R _c =CH ₂ (MDAA); Or
N,N -1,2-ethanediylbis(2-methyl-2-propenamide)
N , N'- ethylene-bis-acrylamide with R _c =CH ₂ -CH ₂ ;
N , N'- butylene-bis-acrylamide with R _c =CH ₂ -CH ₂ -CH ₂ -CH ₂ ;
N , N'- hexylene-bis-acrylamide with R _c = _CH2 - _CH2 - _CH2 - _CH2 - _CH2 - _CH2
(VI ₁₂ )
R _c = (C ₁ -C ₆ )alkylene
R'' = H or (C ₁ -C ₄ )alkyl such as CH ₃ In particular, the crosslinkers of the invention are chosen from(VII ₆ )such as(VII' ₆ ), (VII ₇ )And(VII ₈ ),such as Ethylene Glycol Diacrylate; Tetra(ethylene glycol) diacrylate, and diethylene glycol diacrylate (DEGDA), preferably DEGDA. Dispersion (A), according to any one of the preceding claims, in which the quantity of water v) is between 5% and 40% by weight relative to the total weight of the dispersion, more particularly between 7% and 35% by weight, preferably between 10.8% and 26.0% by weight, relative to the total weight of the dispersion (A). Dispersion (A), according to any one of Claims 1 to 15, in which the said dispersion does not comprise more than 3% by weight of surfactants with respect to the total weight of the dispersion, preferably not more than 2% by weight of surfactants with respect to the total weight of the dispersion, more particularly not more than 1% by weight of surfactants relative to the total weight of the dispersion, even more preferably the composition does not comprise more than 0.5% by weight of surfactants relative to the total weight of the dispersion, even better the mixture does not comprise a surfactant. Dispersion (A), according to any one of the preceding claims, which comprises one or more cosmetic active ingredient(s) vi) chosen from:
- organic and mineral or inorganic pigments,
- special effect pigments such as fluorescent, thermochromic, photochromic pigments, nacres, coated or uncoated, in the form of powder or pigment paste, lacquers, glitter or mixtures thereof;
- said pigments can be dispersed in the product using a dispersing agent and the pigments can be surface-treated with an organic agent;
in particular, the cosmetic active ingredient(s) iv) is (are) chosen from:
- the organic pigments nitroso, nitro, azo, xanthene, quinoline, anthraquinone, phthalocyanine, of metal complex type, isoindolinone, isoindoline, quinacridone, perinone, perylene, diketopyrrolopyrrole, thioindigo, dioxazine, triphenylmethane, quinophthalone;
- white or colored organic pigments which are chosen from carmine, carbon black, aniline black, azo yellow, quinacridone, phthalocyanine blue, sorghum red, blue pigments codified in the Color Index under the BLUE 1 LAKE Cl 42090, 69800, 69825, 73000, 74100, 74160 pigment references, the yellow pigments coded in the Color Index under the Cl references 11680, 11710, 15985, 19140, 20040, 21100, 21108, 47000 , 47005, the green pigments codified in the Color Index under the references Cl 61565, 61570, 74260, orange pigments codified in the Color Index under the references CI 11725, 15510, 45370, 71105, red pigments codified in the Color Index under the references CI 12085 ,12120,12370,12420,12490,14700,15525,15580,15620,15630,15800,15850,15865,15880,17200,26100,45380,45410, 58000, 73360, 73915, 75470, pigments obtained by oxidative polymerization of indole or phenolic derivatives;
- mineral pigments or inorganic pigments chosen iron or chromium oxides, manganese violet, ultramarine blue, chromium hydrate, ferric blue and titanium oxide;
preferably, the cosmetic active ingredient(s) iv) is (are) chosen from carbon black, iron oxides, in particular red, brown or black, and micas coated with iron oxide, triarylmethane pigments, in particular blue and violet, such as BLUE 1 LAKE, azo pigments, in particular red, such as D&C RED 7 alkali metal salt of lithol red such as the calcium salt of lithol red B, more preferably the pigment(s) used are chosen from red iron oxides and azo pigments, in particular red ones, such as D&C RED 7, more preferably red iron oxides. Process for the preparation of the dispersion (A) as defined in any one of the preceding claims, comprising the following successive steps:
- In a ^1st step: the stabilizing polymer (or stabilizing agent ii)) is prepared by mixing the monomer(s) constituting the stabilizing polymer d), or e) as defined in claims 1, 9 or 10 with one or more radical initiators ix), in a solvent called a synthetic solvent, and by polymerizing these monomers, preferably the synthetic solvent comprises iii) one or more liquid fatty substances as defined in Claims 1 , 11 or 12; then is added to the stabilizing polymer ii) thus formed, the monomers constituting a first family of particles i) in particular the monomers a ₁ ) and/or a ₂ ), and a ₃ ), preferably a ₁ ) and a ₃ ), plus preferably a''' ₁ ) and a ₃ ) as defined in any one of claims 1 to 8, and the polymerization of these monomers is carried out by the presence of radical initiator(s) ix); Then
- In a ^2nd step, the composition (B) containing:
A ) monomers chosen from:
A1) a mixture of monomers (M) containing:
- monomers a ₁ ) as defined previously, preferably (C ₁ -C ₄ )(alkyl)acrylate of (C ₁ -C ₄ )alkyl whose group(s) (C ₁ -C ₄ )alkyl are substituted by a hydroxy such as the monomers of formula (I') as defined in claim 8, more preferably 2-hydroxyethyl acrylate;
- and/or monomers a ₂ ) as defined previously
- and monomers a ₃ ) as defined above, preferably of formula (5) such as (meth)acrylic acids, preferably acrylic acid;
said mixture (M) preferably containing only monomers a ₁ ) and a ₃ )
Or
A2) monomers a ₃ ) as defined above, preferably of formula (5) and more particularly acrylic acid;
said composition (B) additionally containing
B) one or more radical initiators ix) in particular alkali metal or alkaline earth metal persulfate(s) such as potassium persulfate,
C) optionally one or more polyols iv) liquid(s) at 20°C and 1 atmosphere as defined in claim 1 or 15, preferably chosen from (C ₂ -C ₆ )alkane-diol and (C ₂ -C ₆ )alkane-triol such as glycerol,
D) optionally one or more cross-linking agents vii) as defined in claim 16, in particular chosen from (VII ₆ ) , (VII' ₆ ), (VII ₇ ) and (VII ₈ ), such as Ethylene Glycol Diacrylate, Tetra(ethylene glycol) diacrylate, and diethylene glycol diacrylate (DEGDA), preferably DEGDA,
E ) optionally one or more neutralizers viii) chosen in particular from organic or inorganic alkaline agents, preferably inorganic such as sodium hydroxide or potassium hydroxide, and
possibly water v),
it being understood that the composition (B) contains C) and/or water v), preferably the aqueous composition (B) comprises: A + B + C + D + E and water v);
the composition (B) is added to the medium obtained in the ^1st step, the polymerization of these monomers being preferably carried out with stirring and preferably with heating for a period particularly between 1 minute and 1 day, more particularly between 30 minutes and 10 hours, such as 7 hours at a temperature below 100°C and above 70°C, such as 90°C; then the medium is left to return to ambient temperature; Then
- if composition (B) does not comprise polyol(s) iv) as defined above, one or more polyol(s) is added to the medium in the ^1st step or in a ^3rd step s) liquid(s) at 20°C and 1 atmosphere iv) as defined in claim 1 or 15, preferably chosen from (C ₂ -C ₆ )alkane-diol and (C ₂ - C ₆ )alkane-triol such as glycerol;
when the synthesis of the stabilizers ii) and of the particles i) is complete, the additional solvent is removed and a mixture i) and ii) is obtained in the liquid fatty substance;
in the event of the presence of cosmetic active ingredient(s) vi) chosen from f) to j) as defined in any one of claims 1, or 19 in the dispersion (A), it (s) can be added during the first stage; according to another variant, the said cosmetic active ingredient(s) vi) is (are) added during the ^2nd stage or after the ^2nd stage; according to another variant, the said cosmetic active ingredient(s) vi) is (are) added during the 3 ^rd step; if the active agent or agents are soluble in water, they are preferably found in the aqueous composition (B) as defined above. Process for treating keratin materials, preferably α) keratin fibres, in particular human ones, such as eyelashes, eyebrows or β) human skin, in particular the lips, comprising the application to said materials of at least one dispersion (A), as defined in any one of claims 1 to 18. Use of a dispersion (A) as defined in any one of Claims 1 to 18 for the treatment of human skin, in particular of the face, preferably for filling in skin imperfections such as wrinkles and fine lines or scars by making up said keratin materials, or for filling in skin imperfections such as wrinkles and fine lines or scars while providing care for said keratin materials, such as moisturizing the skin. Polymeric material (C) obtainable by evaporation of water v) and fatty substance(s) iii) liquid(s) at 20°C and 1 atmosphere, of dispersion (A) as defined in any of claims 1 to 18, preferably the material (C) comprises one or more polyol(s) in an amount greater than or equal to 5% by weight and less than 95% by weight relative to the total weight of the material (C), particularly the amount of polyol(s) is between 10% and 90% by weight relative to the total weight of the material, more particularly between 20% and 80% by weight, more particularly between 30% and 70% by weight, relative to the total material weight (C).