FR2901475A1 - Coloring of dark skin comprises application of a cosmetic composition useful e.g. as auto-bronzing composition, an anti-ring product, dye corrector, comprising a soluble coloring system comprising a natural coloring agent - Google Patents

Abstract

Coloring of dark skin comprises application of a cosmetic composition comprising a soluble coloring system comprising a natural coloring agent in a medium, where the composition has a viscosity higher than 100 centipoises and a covering strength i.e. defined by a contrast ratio of less than 80.

Description

containing as described in patent applications WO 94/15580, WO

  96/36309, WO 96/33690, WO 96/36323, FR-A-2754708. However, these conventional cosmetic compositions do not give complete satisfaction when applied to dark skin. Thus, their high content of filler, such as talc and kaolin, and pigments, such as TiO 2 for example, has the effect of providing on this type of makeup support, a greyish effect, or ashen, which for obvious aesthetic reasons is particularly undesirable. However, it is clear that the decrease in the amount of filler and / or pigment that could be beneficial in terms of brightness of makeup may also be detrimental to the coverage sought parallel to hide the dyschromia for example. In addition, the color effect provided by this type of conventional composition is likely to change over time and in particular to become inhomogeneous in response to secretion of sebum and / or sweat.

  As a result, there remains to date a need for a makeup composition particularly for dark skin, which provides this type of skin a good color homogeneity and satisfactory behavior over time. The document EP 1 433 460 proposes a make-up composition more particularly intended for dark skin, associating with coloring agents reflective particles but for the purpose of providing this type of skin with a lightening effect and therefore distinct from that sought according to the invention. . More specifically, the present invention relates according to one of its aspects, a method of making a dark skin comprising applying to said skin a composition comprising in a physiologically acceptable medium at least one direct coloring system in the state soluble composition, said composition having a viscosity greater than 100 centipoise, and a hiding power, defined by the Contrast Ratio, less than 80. The present invention also aims according to another of its aspects, a method of making a dark skin comprising application to said skin of a composition comprising in a physiologically acceptable medium at least one direct dyeing agent in the soluble state, said composition having a hiding power defined by the Contrast Ratio, less than 80, and a pH greater than 5.

  For the purposes of the present invention, the term "dark skin" means skin whose average lightness L * measured on the forehead, cheekbones and chin in the CIE 1976 color space is less than 55. Saturation C * for example between 10 and 30, especially between 12 and 28. The hue angle values h can be between, for example, about 38 and about 54. Clarity values L * may be less than or equal to 50, or even 45 or 40 for the darker skins, while being able to remain, for most skins, greater than 30. Dark skins are encountered for example among the populations African, African American, Hispanic American, Indian and North African.

  These skins can still be classified on the basis of their reactivity to the effects of solar radiation according to the scale proposed by FITZPATRICK. According to this scale, the different existing ethnic skins can be distinguished according to the following types: Type Reactivity of the skin Origin I Burns always, never bronze Celtic II Burns always, little bronze Germanic III Burns moderately, progressively bronze European IV Burns slightly, bronze very easily Mediterranean V Burns rarely, intensely bronze Middle East - South American VI Never burns, strongly pigmented African The dark skin which is more particularly the subject of the present invention belong to types IV to VI. According to an advantageous embodiment, the compositions considered according to the invention provide a variation of negative clarity AL ranging from -20 to -1 and a variation of saturation AC * ranging from 0.5 to 20 when applied to the zone. B11 + a contrast map as defined in the document EP 1 433 462. This map has 3 times five areas respectively having for colorimetric coordinates, to 15% or even 12.5%, better to 10%, or even to within 7.5%, or even within 5%, for L * and h, and to 25%, better to 20%, even better 15%, or even 10%, or even 5%, for C *, first zone (B1 +): L * = 36.7 C * = 19.81 h = 47.34; second zone (B1): L * = 38.43 C * = 21.76 h = 46, 51, - third zone (B12): L * = 35.66 C * = 19.78 h = 46.32, - fourth zone (B12 +): L * = 32.98 C * = 17.29 h = 44, 64, 5 - fifth zone () OX): L * = 29.63 C * = 15.06 h = 40.34, -second zone (B12): L * = 35.66 C * = 19.78 h = 46.32, - third zone (Cl l): L * = 38.73 C * = 21.94 h = 50.18, - fourth zone (C10): L * = 42.19 C * = 24.18 h = 51.94, first zone (D6): L * = 54.08 C * = 26.70 h = 57.35, - second zone (Cl l): L * 5 = 38.73 C * = 21.94 h = 50, 18, 15 - third zone (D8): L * = 47.94 C * = 26.18 h = 56.82, - fourth zone (D7): L * = 51.79 C * = 27.21 h = 57 , 09, - fifth zone (D5): L * = 57.61 C * = 26.22 h = 55.09, The measurements of the trichromatic coordinates of the composition, L *, C * and h 20 are carried out with a spectrocolorimeter MINOLTA brand, reference CM3700d, in reflection mode, specular included, small opening SAV 5 mm. A composition film is deposited using the BRAVE INSTRUMENTS thermostatically controlled automatic film applicator and a BRAVE INSTRUMENTS calibrated spreader, film thickness: 20 m, on a clear transparent IMPEGA photocopier film. It is allowed to dry for 10 minutes at 37 ° C. in an oven, and this film is superimposed on the contrast card. The color difference between the contrast card through the transparent film and the contrast card is measured through the film thus covered with composition. A = (contrast card + cream film on the transparent film) ù (contrast card with the transparent film). - first zone (C9): L * = 45.04 C * = 25.18 h = 53.27, 10 - fifth zone (C8): L * = 48.06 C * = 25.97 h = 53.09 COVERING POWER Advantageously, the cosmetic compositions according to the invention are characterized by a covering power, defined by the Contrast Ratio, of less than 80, in particular less than or equal to 50.

  This hiding power can be measured by the following method. The measurement is carried out on a film of composition spread on an Erichsen contrast card, type 24/5, presenting a black background and a white background. In the case of a stick, the composition is premixed so as to obtain a viscous paste.

  In the case of a powder, 50 parts by weight of the powder are kneaded with 50 parts by weight of dimethicone (DC 200 Fluid 5CST of DOX CORNING) so as to obtain a viscous paste. The film is spread with a thickness of 50 m on and the trichromatic coordinates (X, Y, Z) are measured using a CM-2002 or CR-3700 colorimeter.

  Similar spreads are made on two other contrast cards and three measurements are made on each card. The average corresponding to these nine measurements is then calculated. The hiding power is equal to 100 x Yn / Yb where Yn is the average value of Y on a black background and Yb is the average value of Y on a white background.

  The higher the value of the report, the higher the hiding power.

  DIRECT COLORING SYSTEM The term "direct coloring system" designates a coloring agent or mixture of coloring agents which, as soon as they come into contact with the make-up support, generally the skin, instantaneously provide an associated coloring effect. Are thus excluded from this definition, the compounds that exert a self-tanning action on human skin in the image of derivatives having a ketone group such as hydroxymethylketones and in particular dihydroxyacetone (DHA) and also methylglyoxane. Indeed, as opposed to the direct dyeing system according to the invention, these compounds cause a non-immediate color effect. The inventors have thus found, unexpectedly, that the use of a direct dyeing system as defined above in a soluble form makes it possible to obtain a homogenizing and radiant result in terms of make-up that is not dull nor ashen. Moreover, the use of such a system makes it possible to substantially increase the makeup behavior over time, in particular in terms of resistance to sweat and / or sebum. Thus, the cosmetic compositions considered according to the invention make it possible to impart to dark skin a coloration having a very good resistance and which advantageously distinguishes itself from the more superficial and evolving colorations, provided by conventional makeup compositions and which are generally formulated Essentially from dispersed pigments. The coloring agent (s) forming the direct dyeing system considered in the context of the present invention may be present in a content ranging from 0.001 to 5%, especially from 0.01 to 3%, and more particularly from 0.025 to 1% by weight relative to the total weight of the composition. The direct dyeing system may comprise at least 30% by weight, in particular at least 50% by weight, in particular at least 65% by weight, more particularly at least 70% by weight, or even at least 75% by weight and more. particularly at least 90% by weight of all the coloring agents present in the composition. According to a particular embodiment, this direct dyeing system comprises all the dyes of said composition. As previously stated, the direct staining system is in a solubilized state within the composition as opposed to conventional formulations in which the coloring agents are essentially formulated in a dispersed state. The coloring agents forming the direct dyeing system can therefore be liposoluble or water-soluble. Advantageously, they are water-soluble. The coloring agents of the direct dyeing system may be synthetic or natural. It can be organic or mineral dyes. Liposoluble, synthetic or natural dyes are, for example, DC Red 17, DC Red 21, DC Red 27, DC Green 6, DC Yellow 11, DC Violet 2, DC Orange 5, red Sudan, carotenes (3-carotene, lycopene), xanthophylls (capsanthin, capsorubin, lutein), palm oil, Sudan brown, quinoline yellow, annatto, curcumin. Examples of these are FDC Red 4, DC Red 6, DC Red 22, DC Red 28, DC Red 30, DC Red 33, DC Orange 4, DC Yellow 5, DC Yellow 6, DC Yellow 8, FDC Green 3, DC Green 5, FDC Blue 1, betanin (beet), carmine, copper chlorophyllin, methylene blue, anthocyanins (enocianin, black carrot, hibiscus, elderberry), caramel, riboflavin.The dyes can be further selected from juglone, lawsone, fermented soybean extracts, algae, mushrooms, microorganisms.Salt Flavyliu m unsubstituted in position 3 such as for example those described in patent EP 1 172 091, extracts of Gesneria Fulgens, Blechum Procerum, Saxifraga and pigments that can be obtained by extraction with an organic or hydro-organic solvent; a micromycete culture medium of the Monascus monascus type.

  In a particular embodiment, the direct dyeing system comprises at least one natural coloring agent, especially as defined above, in particular water-soluble.

  The composition may further comprise dispersed pigments and / or nacres provided that they do not affect the expected properties of the composition. Advantageously, these insoluble coloring agents may be present in a proportion of less than 8% by weight, more particularly less than 5% and especially less than 3% by weight relative to the total weight of the composition. By way of non-limiting illustration of the inorganic pigments, mention may be made more particularly of yellow, red and brown metal oxides, for instance iron oxides. As metal powders, mention may be made of copper powder. The pigments used in the context of the present invention may be used either in their raw form or in a pretreated form, in particular on their surface.

  As representative of these surface treatments, mention may be made in particular of treating the pigment with a hydrophobic and oleofuge agent of the perfluoroalkyl phosphate derivative type as described in patent EP 1 086 683. As an illustration of the pigments which are more particularly suitable for the the invention may especially be mentioned brown iron oxide and yellow iron, coated with perfluoroalkyl phosphate and alumina-treated titanium oxide, coated with perfluoroalkyl phosphate, such as in particular the pigment pastes sold under the trade names YELLOW IRON OXIDE COVAFLUOR, PF5 YELLOW 601 (yellow) and PF5 R516L (red) by the company DAITO, under the trade names FA50DRF, FA50DYF, FA65DF and FA65DBF by the company KOBO. By "nacres", it is necessary to include colored particles of any shape, iridescent or not, in particular produced by certain shellfish in their shell or else synthesized and which exhibit a color effect by optical interference. The nacres may be chosen from pearlescent pigments such as iron oxide-coated titanium mica, bismuth oxychloride-coated mica, titanium mica coated with chromium oxide, titanium mica coated with an organic dye. especially of the aforementioned type as well as pearlescent pigments based on bismuth oxychloride. It may also be mica particles on the surface of which are superimposed at least two successive layers of metal oxides and / or organic dyestuffs. The nacres may more particularly have a color or a yellow, pink, red, bronze, orange, brown, gold and / or coppery reflection. As an illustration of nacres that can be used in the context of the present invention, mention may be made especially of gold-colored nacres sold especially by ENGELHARD under the name Brillant gold 212G (Timica), Gold 222C (Cloisonne), Sparkle gold (Timica), Gold 4504 (Chromalite) and Monarch gold 233X (Cloisonne); bronze nacres sold especially by the company Merck under the name Bronze Fine (17384) (Colorona) and Bronze (17353) (Colorona) and by Engelhard under the name Super Bronze (Cloisonne); orange nacres sold especially by the company Engelhard under the name Orange 363C (Cloisonne) and Orange MCR 101 (Cosmica) and by the company Merck under the name Passion Orange (Colorona) and Matte Orange (17449) (Microna); brown-colored pearlescent agents marketed by Engelhard under the name Nu-antique copper 340XB (Cloisonne) and Brown CL4509 (Chromalite); nacres with a copper sheen sold especially by Engelhard under the name Copper 340A (Timica); the nacres with a red glint sold especially by MERCK under the name Sienna fine (17386) (Colorona); yellow-colored pearlescent agents marketed by ENGELHARD under the name Yellow (4502) (Chromalite); the red-colored pearlescent agents with a gold glint sold especially by ENGELHARD under the name Sunstone G012 (Gemtone); pink nacres sold especially by Engelhard under the name Tan opal G005 (Gemtone); the black nacres with gold reflection sold by the company Engelhard under the name Nu antique bronze 240 AB (Timica), the blue nacres sold especially by the company Merck under the name Matte Blue (17433) (Microna), the white nacres with reflection silver sold in particular by the company Merck under the name Xirona Silver and the golden-green orange-colored mother-of-pearl marketed by Merck under the name Indian summer (Xirona) and their mixtures. The compositions according to the invention may also comprise, as additional coloring agent, one or more compounds which exert a self-tanning action on human skin, in the image of derivatives having a ketone group such as hydroxymethylketones and in particular dihydroxyacetone ( DHA) and also methylglyoxane.

  PHYSIOLOGICALLY ACCEPTABLE MEDIUM "Physiologically acceptable medium" means a non-toxic medium that can be applied to the skin of human beings. The physiologically acceptable medium is generally adapted to the nature of the skin on which the composition is to be applied as well as to the form in which the composition is intended to be packaged, in particular fluid at ambient temperature and at atmospheric pressure.

  As stated above, the compositions of the invention are more particularly compositions intended for the make-up of the skin and in particular of the skin of the face. It can thus be basic compositions and / or foundation type.

  They can be solid or liquid and are advantageously formulated in a fluid form. Thus they may be in an anhydrous form or in the form of a gel, direct emulsion, inverse or multiple associating at least one aqueous phase and at least one fatty phase.

  As previously stated, they advantageously have a viscosity greater than 100 centipoise, in particular greater than or equal to 300 centipoises. This viscosity can be measured by the following method. The measurement is carried out using a Rheomat RM 180 type viscometer. The product is poured into the cup adapted to the mobile used, depending on the fluidity of the product. The viscosity is measured after 10 minutes of rotation, at a speed of 75 seconds, and at room temperature.

  Aqueous Phase The compositions according to the invention may comprise at least one aqueous medium, constituting an aqueous phase, which can form the continuous phase of the composition in question. The aqueous phase can consist essentially of water. It may also comprise a mixture of water and water-miscible organic solvent (miscibility in water greater than 50% by weight at 25 ° C.) such as lower monoalcohols having from 1 to 5 carbon atoms such as ethanol, isopropanol, glycols having 2 to 8 carbon atoms such as propylene glycol, ethylene glycol, 1,3-butylene glycol, dipropylene glycol, C3-C4 ketones, and aldehydes in C2-C4. According to a particular embodiment, the lower monoalcohol type solvent in the context of the present invention may represent from 1 to 70%, and preferably from 2 to 50% by weight of the composition used in the claimed process. As an example of a monoalcohol suitable for carrying out the invention, mention may be made of saturated hydrocarbon compounds comprising a single hydroxyl function and comprising from 2 to 15 carbon atoms, in particular from 4 to 12 carbon atoms. .

  By way of example of a monoalcohol that is suitable for the invention, mention may be made, in a nonlimiting manner, of ethanol, propanol, isopropanol, butanol, pentanol, propanol, hexanol, heptanol octanol, decanol and dodecanol. The term "polyhydroxylated solvent" is intended to cover any hydrocarbon compound comprising at least two hydroxyl functions and comprising from 4 to 40 carbon atoms, in particular from 6 to 36 carbon atoms, in particular from 8 to 32 carbon atoms, in particular from 16 to 28 carbon atoms, and more particularly from 18 to 24 carbon atoms. The hydrocarbon chains may, where appropriate, be interrupted by the presence of at least one heteroatom, and in particular an oxygen atom. The polyol suitable for the implementation of the present invention may be, in particular, selected from linear, branched, cyclic or polycyclic alcohols, saturated or unsaturated. Thus, the polyol may be selected for example from a diol, a triol, a tetraol, or a pentaol, or an ester thereof. The polyol may be a diol, or an ester thereof, for example chosen from a fatty alcohol dimer, a mono- or poly-glycerol, a C 2 -C 4 mono- or poly-alkylene glycol, 1,4 butanediol, and pentaerythritol. By way of example of a diol which may also be suitable for carrying out the invention, non-exhaustive examples include butanediol, pentanediol, propanediol, hexanediol, hexylene glycol, heptanediol and the like. , octanediol, nonanediol, decanediol, 1-decanediol, dodecanediol, tridecanediol, tetradecanediol, pentadecanediol, hexadecanediol, nonadecanediol, octadecenediol, cyclohexanediol, 1,1'-oxydipropanediol diglycerol, erythritol, pentaerythritol, xylitol, sorbitol, phytantriol (3,7,11,15-tetramethyl-1,2,3-trihydroxyhexadecane) ethylene glycol, xylene glycol and their isomers. Particularly suitable as a mixture is a mixture based at least on ethanol and propylene glycol or dipropylene glycol or butylene glycol. The aqueous phase (water and optionally the water-miscible organic solvent (s)) can be present at a content ranging from 1% to 99% by weight, in particular ranging from 3% by weight. % to 80% by weight, and in particular ranging from 5% to 60%, by weight relative to the total weight of the composition in question.

  Grime phase The composition according to the invention may comprise a fatty phase and in particular at least one fatty substance which is liquid at room temperature (25 ° C.) and / or a fatty substance which is solid at ambient temperature, such as waxes, pasty fatty substances, gums and their mixtures. The fatty phase may further contain lipophilic organic solvents. The composition may for example have a continuous fat phase, which may contain less than 5% water, especially less than 1% water relative to its total weight and in particular be in anhydrous form. The fatty phase of the composition according to the invention may in particular comprise, as liquid fatty substance, at least one volatile or non-volatile oil or a mixture thereof. For the purposes of the invention, the term "volatile oil" means any oil capable of evaporating on contact with the skin in less than one hour at ambient temperature and atmospheric pressure. The volatile oils of the invention are volatile cosmetic oils, which are liquid at room temperature, having a non-zero vapor pressure, at ambient temperature and atmospheric pressure, in particular from 0.01 to 300 mmHg (1.33 Pa at 40,000 Pa) and preferably greater than 0.3 mm Hg (30 Pa). By "non-volatile oil" is meant an oil remaining on the skin at room temperature and atmospheric pressure for at least several hours and having in particular a vapor pressure of less than 0.01 mmHg (1.33 Pa). These volatile or non-volatile oils may be hydrocarbon oils, silicone oils, or mixtures thereof. The term "hydrocarbon-based oil" means an oil containing mainly hydrogen and carbon atoms and optionally oxygen, nitrogen, sulfur and phosphorus atoms. The volatile hydrocarbon-based oils may be chosen from hydrocarbon-based oils containing from 8 to 16 carbon atoms, and especially C 8 -C 16 branched alkanes such as C 8 -C 16 isoalkanes of petroleum origin (also called isoparaffins), such as isododecane. (also known as 2,2,4,4,6-pentamethylheptane), isodecane, isohexadecane, and for example the oils sold under the trade names Isopars 30 or permetyls, branched Cg-C16 esters such as as isohexyl neopentanoate, and mixtures thereof. Other volatile hydrocarbon oils such as petroleum distillates, especially those sold under the name Shell Solt by Shell, can also be used. As volatile oils, it is also possible to use volatile silicones, for example volatile linear or cyclic silicone oils, in particular those having a viscosity of 8 centistokes (8 × 10 -6 m 2 / s), and having in particular from 2 to 7 silicon atoms, these silicones optionally having alkyl or alkoxy groups having from 1 to 10 carbon atoms. As volatile silicone oil that can be used in the invention, there may be mentioned in particular octamethylcyclotetrasiloxane, decamethylcyclopentasiloxane, dodecamethylcyclohexasiloxane, heptamethylhexyltrisiloxane, heptamethyloctyltrisiloxane, hexamethylisiloxane, octamethyltrisiloxane and decamethyl tetrasiloxane, dodecamethylpentasiloxane and mixtures thereof. The volatile oil may be present in a composition according to the invention at a content ranging from 0.1 to 98% by weight, especially from 1% to 65% by weight, and in particular from 2% to 50% by weight. relative to the total weight of the composition.

  The non-volatile oils may in particular be chosen from non-volatile fluorinated hydrocarbon oils and / or silicone oils. Non-volatile hydrocarbon oils that may especially be mentioned include: - hydrocarbon-based oils of animal origin, - hydrocarbon-based oils of plant origin, such as triglycerides consisting of esters of fatty acids and of glycerol, the fatty acids of which may have chain lengths varied from C4 to C24, the latter being linear or branched, saturated or unsaturated; these oils include wheat germ, sunflower, grape seed, sesame, maize, apricot, castor, shea, avocado, olive, soya, sweet almond oil , palm, rapeseed, cotton, hazelnut, macadamia, jojoba, alfalfa, poppy, pumpkin, sesame, pumpkin, rapeseed, blackcurrant, evening primrose, millet, barley quinoa, rye, safflower, bancoulier, passionflower, muscat rose; shea butter; or alternatively caprylic / capric acid triglycerides, such as those sold by Stéarineries Dubois or those sold under the names Miglyol 810, 812 and 818 by the company Dynamit Nobel, synthetic ethers having from 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, and mixtures thereof; synthetic esters, such as oils of formula R1000R2 in which R1 represents the residue of a linear or branched fatty acid containing from 1 to 40 carbon atoms and R 2 represents a particularly branched hydrocarbon-based chain containing from 1 to 40 carbon atoms, provided that R 1 + R 2 is 10, for example oil of purcellin (cetostearyl octanoate), isopropyl myristate, isopropyl palmitate, C12-C15 alcohol benzoates, hexyl laurate, diisopropyl adipate, isononyl isononanoate, 2-ethylhexyl palmitate, isostearyl isostearate, heptanoates, octanoates, decanoates or ricinoleates of alcohols or polyalcohols such as propylene glycol dioctanoate; hydroxylated esters such as isostearyl lactate, diisostearyl malate; polyol esters and pentaerythritol esters, branched-chain and / or unsaturated carbon-chain liquid fatty alcohols having from 12 to 26 carbon atoms, such as octyl dodecanol, isostearyl alcohol and oleic alcohol, 2-hexyldecanol, 2-butyloctanol, 2-undecylpentadecanol, - higher fatty acids such as oleic acid, linoleic acid, linolenic acid and mixtures thereof.

  The non-volatile silicone oils that may be used in the composition according to the invention may be non-volatile polydimethylsiloxanes (PDMS), polydimethylsiloxanes comprising alkyl or alkoxy groups, during and / or at the end of the silicone chain, groups each having from 2 to 24 carbon atoms, phenyl silicones such as phenyl trimethicones, phenyl dimethicones, phenyl trimethylsiloxy diphenylsiloxanes, diphenyl dimethicones, diphenyl methyldiphenyl trisiloxanes, 2-phenylethyl trimethylsiloxysilicates. The non-volatile oils may be present in a composition according to the invention in a content ranging from 0.01 to 90% by weight, especially from 0.1 to 85% by weight, and in particular from 1% to 70% by weight. , relative to the total weight of the composition.

  More generally, the liquid fatty substance may be present in a proportion of 0.01 to 90% by weight and especially 0.1 to 85% by weight, relative to the weight of the fatty phase. Regarding the solid fat at room temperature and at atmospheric pressure, it may be chosen from waxes, pasty fatty substances, gums and mixtures thereof. This solid fatty substance may be present in a proportion of from 0.01 to 50%, especially from 0.1 to 40% and in particular from 0.2 to 30% by weight, relative to the total weight of the fatty phase. Thus, a composition according to the invention may comprise at least one pasty fat compound at room temperature. For the purposes of the invention, the term "pasty fatty substance" means fatty substances having a melting point ranging from 20 ° to 55 ° C., preferably 25 ° to 45 ° C., and / or a viscosity at 40 ° C. ranging from 0.1 ° C. at 40 Pa.s (1 to 400 poises), preferably 0.5 to 25 Pa.s, measured with Contraves TV or Rhéomat 80, equipped with a mobile rotating at 60 Hz. The person skilled in the art can choose the mobile device for measuring viscosity, among mobile MS-r3 and MS-r4, on the basis of his general knowledge, so as to be able to measure the pasty compound tested. Preferably, these fatty substances are hydrocarbon compounds, optionally of polymeric type; they can also be chosen from silicone compounds; they may also be in the form of a mixture of hydrocarbon compounds and / or silicone. In the case of a mixture of different pasty fatty substances, use is preferably made of hydrocarbon-based pasty compounds (mainly containing carbon and hydrogen atoms and optionally ester groups), in majority proportion. Among the pasty compounds which may be used in a composition according to the invention, mention may be made of lanolins and lanolin derivatives, such as acetylated lanolines, oxypropylenated lanolins or isopropyl lanolate, having a viscosity of 18 to 21%. Pa.s, preferably 19 to 20, 5 Pa.s, and / or a melting point of 30 to 55 C and mixtures thereof. It is also possible to use esters of fatty acids or alcohols, in particular those having 20 to 65 carbon atoms (melting point of about 20 to 35 ° C. and / or viscosity at 40 ° C. of from 0.1 at 40 Pa. $) such as tri-isostearyl citrate or cetyl citrate; arachidyl propionate; vinyl polylaurate; esters of cholesterol such as triglycerides of plant origin such as hydrogenated vegetable oils, viscous polyesters such as poly (12-hydroxystearic acid) and mixtures thereof. As vegetable triglyceride, hydrogenated castor oil derivatives such as Rheox's "THIXINR" can be used.

  Mention may also be made of silicone pasty fatty substances such as polydimethylsiloxanes (PDMS) of high molecular weight and in particular those having pendent chains of the alkyl or alkoxy type having from 8 to 24 carbon atoms, and a melting point of 20- C, such as stearyl dimethicones, especially those sold by Dow Corning under the trade names DC2503 and DC25514, and mixtures thereof. The pasty fatty substance may be present in a composition according to the invention in a content ranging from 0.01 to 50% by weight, preferably ranging from 0.1 to 45% by weight, and better still ranging from 0.2% to 30% by weight, relative to the total weight of said composition. The composition according to the invention may further comprise a wax. The wax may be solid at room temperature (25 ° C.), with reversible solid / liquid state change, having a melting point greater than 30 ° C., up to 200 ° C., a hardness greater than 0.5 MPa, and having the solid state an anisotropic crystalline organization. It can be hydrocarbon, fluorinated and / or silicone and be of animal, vegetable, mineral or synthetic origin. It may be chosen for example from beeswax, carnauba wax, candellila wax, paraffin waxes, hydrogenated castor oil, silicone waxes, microcrystalline waxes, and mixtures thereof. In particular, the wax may be present in the form of a wax-in-water emulsion. The wax may be present in a composition according to the invention in a content ranging from 0.01% to 50% by weight, in particular from 0.1% to 30% by weight, and especially from 0.2% to 20% by weight. by weight, relative to the total weight of the composition.

  Surfactants The composition may further contain emulsifying surfactants present in particular in a proportion ranging from 0.1 to 30% by weight, and better still from 5% to 15% by weight, relative to the total weight of the composition. These surfactants may be chosen from anionic or nonionic surfactants. Reference can be made to "Encyclopedia of Chemical Technology, KIRK-OTHMER", volume 22, p.333-432, 3rd edition, 1979, WILEY, for the definition of the properties and functions (emulsifier) of surfactants, in particular .347-377 of this reference, for anionic and nonionic surfactants. The surfactants preferably used in the composition of the foundation type according to the invention are chosen: - from the nonionic surfactants: fatty acids, fatty alcohols, polyethoxylated or polyglycerolated fatty alcohols such as polyethoxylated stearyl or cetylstearyl alcohols, sucrose fatty acid esters, alkyl glucose esters, in particular polyoxyethylenated C1-C6 alkyl glucose fatty esters, and mixtures thereof; - among the anionic surfactants: C16-C30 fatty acids neutralized by the amines, ammonia or alkaline salts, and mixtures thereof. - Among the silicone surfactants chosen from the compounds of the following general formula (I): ## STR1 ## in which: R 1 and R 4, which may be identical or different, represent a hydrogen atom or a linear or branched alkyl radical; C1-C30 or a phenyl radical, R2, which are identical or different, represent - (CxH2x) - (OC2H4) a- (OC3H6) b-20 OR3, - R3, which may be identical or different, are chosen from a hydrogen atom; a linear or branched alkyl radical having from 1 to 12 carbon atoms, an acyl radical, linear or branched having from 2 to 12 carbon atoms, n varies from 1 to 1000, 25 - p varies from 30, - a varies from 50, - b varies from 50, - xvariedel to 5. The number average molecular weight of this silicone emulsifier is generally greater than or equal to 15,000 and preferably from 20,000 to 40,000.

  A first family of polyalkyl polyether siloxanes which are particularly suitable for the compositions according to the invention is that of the compounds corresponding to formula (I) above for which the radicals R 1 and R 4 are identical and all represent methyl radicals and the radical R 3 represents hydrogen.

  By way of example of a silicone emulsifier belonging to this family, mention may be made of the oxyethylenated oxypropylenated poly (ethylene / methyl siloxane) (EO / OP 18/18) for which n is 396 and p is 4, with a number of molecular weight greater than 30,000 (CTFA name: Cyclomethi-cone 90% dimethicone copolyol 10%) sold under the trade name "Si-licone Q2-3225C" by Dow Corning.

  In the above definition and in the following text, OE represents one mole of ethylene oxide and OP represents one mole of propylene oxide. A second family of polyalkyl polyether siloxanes particularly suitable for the compositions according to the invention is that of the compounds corresponding to the formula (I) above for which the radicals RI are all methyl radicals and the radicals R4 are all lauryl radicals. A particularly preferred silicone emulsifier of this second family is the oxyethylenated oxypropylenated poly (meth / yl) / (18/18) poly (methyl / ethyl) siloxane for which n is 35 and p is 3, with a number of molecular weight greater than 25,000 (CTFA name: 91% Lauryl-Methicone Copolyol, Isostearyl Alcohol 9%) sold under the trade name "DC Q2-5200" by the company Dow Corning.

  A particularly preferred silicone emulsifier for the compositions according to the invention is an oxyalkylene silicone substituted in linear structure, substituted at both ends of the main chain by oxyalkylene groups connected to the Si atoms via a grouping. hydrocarbon. More particularly, a silicone corresponding to the following general formula (II) will be chosen: ## STR2 ## in which: R = - (CH 2) s O- (C 2 H 4 O) t (C 3 H 6 O) uR 1 where: R 1 represents H, CH 3 or CH 2 CH 3, s is an integer ranging from 1 to 5, t varies from 1 to 100, u varies from 0 to 50, the units (C2H40) and (C3H60) being randomly distributed or in blocks,

  or - the radicals R 2 represent a C 1 -C 3 alkyl radical or a phenyl radical, - 5 <m <300,

  Preferably, the substituted oxyalkylenated silicone used according to the present invention has the general formula (II) for which all the radicals R 2 are methyl radicals and: - svade 2 to 4, - t is from 3 to 100, - m ranges from 50 to 200.

  More preferably, the average molecular weight of R is from 800 to 2600.

  Preferably, the weight ratio of C2H40 units to C3H60 units is from 100: 10 to 20:80. Advantageously, this ratio is approximately 42/58.

  More preferably, R 1 is methyl. Even more preferably, the emulsion according to the invention comprises the oxyalkylenated silicone with the following formula: ## STR2 ## in which: m = 100, - R = (CH2) 3-O- (C2H40) x- (C3H60) y-CH3, where t is from 3 to 100, u is from 1 to 50, the weight ratio of the number of C2H40 to the number of C3H60 being about 42/58, the average molecular weight of R ranging from 800 to 1000.

  Among the commercial products which may contain all or part of the oxyalkylenated silicones which may be used according to the invention as emulsifiers, mention may be made in particular of those sold under the names "Abil EM 97" by Gold-schmidt or " KF 6009 "," X22-4350 "," X22-4349 "or" KF 6008 "by Shin Etsu Company.

  The polyalkyl polyether siloxane emulsifier as defined above is used according to the invention in a preferential proportion ranging from 0.1 to 30% and more particularly from 0.5 to 10% by weight relative to the total weight of the emulsion.

  Film-forming polymer The composition according to the invention may comprise, in addition, at least one film-forming polymer. According to the present invention, the term "film-forming polymer" means a polymer capable of forming on its own or in the presence of an auxiliary film-forming agent, a continuous and adherent film on the skin. A film-forming polymer capable of forming a hydrophobic film, that is to say a polymer whose film has a solubility in water at 25 ° C. of less than 1% by weight, is preferably used.

  The film-forming polymer may in particular be at least one polymer chosen from the group comprising: water-soluble film-forming polymers; aqueous dispersions of particles of film-forming, water-dispersible polymers, also called "latices"; in this case, the composition should comprise an aqueous phase, liposoluble film-forming polymers, lipodispersible film-forming polymers in the form of nonaqueous dispersions of polymer particles, preferably dispersions of polymeric particles, optionally stabilized on their surface. by at least one stabilizing agent, in one or more silicone and / or hydrocarbon oils; these non-aqueous dispersions are still called "NAD". The film-forming polymer may be present in a composition according to the invention in a solids content ranging from 0.01% to 20% by weight relative to the total weight of the composition and in particular from 0.5% to 10% by weight. weight. Among the film-forming polymers that may be used according to the invention, mention may be made of synthetic polymers, of radical type or of polycondensate type, polymers of natural origin, and their mixtures. By radical-forming film-forming polymer is meant a polymer obtained by polymerization of unsaturated monomers, especially ethylenic monomers, each monomer being capable of homopolymerizing (unlike polycondensates). The radical-type film-forming polymers may in particular be vinyl polymers or copolymers, in particular acrylic polymers. As the aqueous dispersion of film-forming polymer, it is possible to use the acrylic dispersions sold under the names NEOCRYL XK-90, NEOCRYL A-1070, NEOCRYL A-1090, NEOCRYL BT-62, NEOCRYL A-1079 and NEOCRYL A-523 by the company AVECIA-NEORESINS, DOW LATEX 432 by the company DOW CHEMICAL, DAITOSOL 5000 AD by the company DAITO KASEY KOGYO; or else the aqueous polyurethane dispersions sold under the names 30 NEOREZ R-981, NEOREZ R-974 by the company AVECIA-NEORESINS, the AVALURE UR-405, AVALURE UR-410, AVALURE UR-425, AVALURE UR-450, SANCURE 875, SANCURE 861, SANCURE 878, SANCURE 2060 by the company GOODRICH, IMPRANIL 85 by the company BAYER, AQUAMERE H-1511 by the company HYDROMER. Examples of water-soluble film-forming polymers that may be mentioned include anionic, cationic, amphoteric or non-ionic proteins, chitin or chitosan polymers, cellulose polymers, acrylic polymers or copolymers, vinyl polymers and the original polymers. natural, possibly modified, and mixtures thereof. The film-forming polymer may also be present in the form of particles, surface-stabilized, dispersed in the liquid fatty phase. Dispersions of film-forming polymer in the liquid fatty phase, in the presence of stabilizing agents, are described in particular in documents EP-A-749746, EP-A-923928 and EP-A-930060. Liposoluble film-forming polymers that can be used in the invention also include polyalkylenes and especially copolymers of C2-C20 alkenes, such as polybutene, and alkylcelluloses with a linear or branched alkyl radical, whether or not saturated with C1 to C8, such as ethylcellulose and propylcellulose, copolymers of vinylpyrrolidone (VP) and in particular copolymers of vinylpyrrolidone and of C2 to C40 and better still of C3 to C20 alkene. By way of example of a copolymer of VP which may be used in the invention, mention may be made of the copolymer of VP / vinyl acetate, VP / ethyl methacrylate, polyvinylpyrrolidone (PVP) butylated, VP / ethyl methacrylate / methacrylic acid, VP / eicosene, VP / hexadecene, VP / triacontene, VP / styrene, VP / acrylic acid / lauryl methacrylate.

  The composition according to the invention may further comprise an auxiliary film-forming agent promoting the formation of a film with the film-forming polymer. Such a film-forming agent may be chosen from all the compounds known to those skilled in the art as being capable of fulfilling the desired function, and in particular be chosen from plasticizers and coalescing agents.

  CHARGE Of course, it remains possible to introduce into the composition according to the invention one or more conventional fillers provided that they are used in an amount such that they do not affect the aesthetic effect sought by the compositions considered according to the invention. invention, that is to say do not overly give a greyish appearance to the makeup skin when it is coated with a composition according to the invention. The man of the art is able, by his knowledge, to make this adjustment.

  These fillers can be mineral or organic of any form, platelet, spherical or oblong, regardless of the crystallographic form (for example sheet, cubic, hexagonal, orthorhombic, etc.). Mention may be made of talc, mica, silica, kaolin, polyamide (nylon) powders (Orgasol from Atochem), poly-13-alanine and polyethylene, tetrafluoroethylene polymer powders (Teflon e), lauroyl-lysine, starch, boron nitride, polymeric hollow microspheres such as those of polyvinylidene chloride / acrylonitrile such as Expancel (Nobel Industrie), copolymers of acrylic acid (Polytrap Dow Corning) or polymethyl methacrylate (Wackherr's Covabead), silicone resin microbeads (eg Toshiba's Tospearls), elastomeric polyorganosiloxane particles, precipitated calcium carbonate, magnesium carbonate and magnesium carbonate, hydroxyapatite, hollow silica microspheres (Silica Beads from Maprecos), glass or ceramic microcapsules, metal soaps derived from organic carboxylic acids having 8 to 22 carbon atoms, preferably from 12 to 18 carbon atoms, for example zinc, magnesium or lithium stearate, zinc laurate, magnesium myristate and mixtures thereof. In this case, the compositions according to the invention may contain less than 15% or even less than 5% by weight filler, or may be free under load. It may be advantageous to favor the choice of transparent fillers, such as fumed silica, polymethyl methacrylate (PMMA). The composition considered according to the invention is generally in the form of a makeup base composition, a foundation especially to be applied to the face or neck, a concealer product, a concealer complexion, tinted cream or makeup base for the face or a make-up composition for the body. The composition according to the invention may be in the form of a fluid, for example pasty or liquid. It may be in the form of a soft paste, an ointment, a solid or fluid cream ointment. For example, it may be an oil-in-water, water-in-oil or multiple emulsion, a solid emulsion, especially of water-in-oil type, a gel that is in particular anhydrous, solid or flexible and even in two-phase form.

  It can also be in solid form, for example powdery, compacted or cast or stick form. The invention will be better understood on reading the detailed description which follows, non-limiting examples of implementation thereof.

  EXAMPLES Example 1: Colored oil-in-water emulsion-type cosmetic composition - Dialkyl tartrate (C14-15 linear) mixture, cetylstearyl alcohol, lauryl alcohol, oxyethylene (25 OE), oxypropylene (2) (COSMACOL PSE from SASOL) 1.500 Mixture mono / glyceryl distearate / polyethylene stearate 2,000glycol (100 OE) (UNIQUEMA ARLACEL 165 FL) Stearyl alcohol (95% C18) (COGNIS LANETTE 18) 1,000 Cyclohexa dimethylsiloxane (Dow Corning 246 FLUID 7,500 Dow Corning) Isoparaffin Hydrogenated (6-8 moles of isobuthylene) (PARLEAM 2,500 of NOF CORPORATION) - Butyl P-hydroxybenzoate (distributed by UENO FINE CHEMICALS) Protected 2-ethyl hexyl 0,150 - 4-methoxycinnamate (DSM NUTRITIONAL PRODUCTS PARSOL MCX) 1,000 B1 - Water 52,500 - Methyl hydroxybenzoate (distributed by NIPA) 0.250 - Chlorphenesin (from DENK (MERCK)) 0.250 B2 - Water 16.350 - Di-sodium salt of tartrazine (CI: 19140) (LCW 08005 FD and C YELLOW 5 ( SENSIENT) 0.255 - Salt of i-sodic bright yellow FCF (CI: 15985) (37001 FD & C YELLOW N 6 from UNIVAR) 0.302 -Salt di-sodium bright green FCF (CI: 42053) (06503 FD & C GREEN 3 from LCW (SENSITIVE) ) 0.035 - Di-sodium salt of acid fuchsin D (CI: 17200) (LCW SENSIENT K7057 D and C RED 33) 0.158 C - Water 1,000 - Chlorhexidine digluconate in solution (chlorhexidine digluconate 20% solution BP / PH. EUR. of SCHUTZ DISHMAN BIOTECH) 0,250 D - Water 9,750 - Sodium hyaluronate (MW: 1,100,000) powder (CRYSTALHYAL from SOLIANCE) E - Corn starch esterified with octenylsuccinic anhydride, aluminum salt (DRY FLO PLUS (28-1160 ) (EUROPE) from NATIONAL STARCH)

  Procedure: Weigh A in a 400 ml beaker which is placed in a water bath at 75 C until complete dissolution.

  The various constituents of the B1 phase are weighed in the main beaker (800 ml) and B2 phase in a 250 ml beaker and are then placed in a 75 C water bath until complete dissolution. When the 2 phases are well dissolved B2 is added in B1 with magnetic stirring. Phase D (gel) is prepared in parallel with Raynerie.

  The emulsion is at 75 ° C. For this, the fatty phase A is poured into the aqueous phase B, increasing as the stirring speed increases to 1500 rpm. There must always be a little vortex. The mechanical stirring is maintained for 10 minutes. The temperature is then lowered to 45 ° C., and phase C is added (stirring for 5 minutes), then phase D (stirring for 5 minutes), then phase E (stirring for 10 minutes). 0,250 3,000 This staining base makes it possible to obtain on the dark skin a neutral brown hue. The measured hiding power (Contrast Ratio) with this staining base is 24.23 and its viscosity is 346 centipoise.

  EXAMPLE 2 Colored Oil-in-Water Emulsion Cosmetic Composition A-Dialkyl Tartrate (Linear C14-15) Mix, Cetylstearyl Alcohol, 1,500 Oxyethylene Lauryl Lauryl (25 OE) Oxypropylene (2) (COSMACOL PSE from SASOL) - Mixture mono / glyceryl distearate / polyethylene glycol stearate (100 OE) (UNIQUEMA ARLACEL 165 FL) 2,000 - stearyl alcohol (95% C18) (COGNIS LANETTE 18) 1,000 - Cyclohexa dimethylsiloxane (DOW CORNING 246 FLUID from Dow Corning) Hydrogenated 7,500 - isoparaffin (6-8 moles of isobuthylene) (NOF CORPORATION PARLEAM) 2,500 - Butyl P-hydroxybenzoate (distributed by UENO FINE 0,150 - CHEMICALS) Protected 2-ethyl hexyl 4-methoxycinnamate (DSM NUTRITIONAL PARSOL MCX) PRODUCTS) 1,000 B1 - Water 52,500 - Methyl hydroxybenzoate (distributed by NIPA) 0,250 - Chlorphenesin (from DENK (MERCK)) 0,250 B2 - Water 16,129 - Di-sodium salt of culvert SX (CI: 14700) (07004 FD and C RED 4 of LCW (SENSIENT)) 0.385 - Salt di-s bright yellow FCF (CI: 15985) (UNIVAR 37001 FD & C YELLOW N 6) 0.500 - Bright green di-sodium salt FCF (CI: 42053) (06503 FD & C GREEN 3 from LCW (SENSIENT) 0.048 D-sodium salt of acid fuchsin D (CI: 17200) (LCW SENSIENT K7057 D and C RED 33) 0.038 C - Water 1.000 - Chlorhexidine digluconate in solution (chlorhexidine digluconate 20% solution BP / PH. EUR. of SCHUTZ DISHMAN BIOTECH) 0,250 D - Water 9,750 - Sodium hyaluronate (MW: 1,100,000) powder (CRYSTALHYAL of SOLIANCE) 0,250 E - Corn starch esterified with octenylsuccinic anhydride, salt 3,000 of aluminum (DRY FLO PLUS (28 The procedure is the same as that of Example 1. This coloring base makes it possible to obtain on a dark skin a red-brown hue. The measured hiding power (Contrast Ratio) with this staining base 5 is 25.5 and its viscosity is 490 centipoise. EXAMPLE 3 Colored Oil-in-Water Emulsion Cosmetic Composition Based on Natural Dyes A - Dialkyl Tartrate Mix (C14-15 Linear), Cetearyl Alcohol, 1,500 Lauryl Oxygen (25 OE) Oxypropylene (2) (COSMACOL PSE) of SASOL) - Mono / glyceryl distearate / polyethylene glycol stearate (100 0E) blend (UNIQUEMA ARLACEL 165 FL) 2,000 - Stearyl alcohol (95% C18) (COGNIS LANETTE 18) 1,000 - Cyclohexa dimethylsiloxane (DOW CORNING 246) DOW CORNING FLUID) 7,500 - Isoparaffin (6-8 moles of isobuthylene) hydrogenated (PARLEAM of NOF CORPORATION) 2,500 - Butyl P-hydroxybenzoate (distributed by UENO FINE 0,150 - CHEMICALS) Protected 2-ethyl hexyl 4-methoxycinnamate ( PARSOL MCX from DSM NUTRITIONAL PRODUCTS) 1,000 B1 - Water 50,000 - Methyl hydroxybenzoate (distributed by NIPA) 0,2505 - Chlorphenesin (from DENK (MERCK)) 0,250 B2 - Water 3,615 - Beetroot extract (Beetroot juice P-WS (4) / 96) of LCW (SENSIENT) 1 3,760 - Beta Carotene Extract (B-Carotene 10% P-WS) from LCW (SENSIENT) 2,190 - LCW (SENSIENT) Copper Chlorophyllin Sodium (97/3) Sodium Salt) 0.035 C - Water 1,000 - Digluconate chlorhexidine solution (chlorhexidine digluconate 20% solution BP / PH. EUR. of SCHUTZ DISHMAN BIOTECH) 0.250 D Water 9,750 - Sodium hyaluronate (MW: 1,100,000) powder (CRYSTALHYAL from SOLIANCE) 0,250 E-Corn starch esterified with octenylsuccinic anhydride, 3,000 aluminum salt (DRY FLO PLUS (28- 1160) (EUROPE) by NATIONAL STARCH) The procedure is the same as that of Example 1. This staining base makes it possible to obtain on a dark skin a tanned hue.

  EXAMPLE 4 Composition of the Foundation Type in the Form of a Solid Al-Cire Candelilla Purified Emulsion (NC 1630 by CERA RICA NODA) 1,800 - Hydrocarbon Mineral Wax (C20 / C60) (Ozokerite wax SP 1020 P from STRAL & PITSCH) 1,200 - Propyl p-hydroxybenzoate (NIPA (CLARIANT)) 0.300 -Poly methylcetyl dimethyl methylsiloxane oxyethylene (20/75/5 ù viscosity: 3000 CST) (Abil EM 90 from GOLDSCHMIDT (DEGUSSA)) 2,000 - Isononanoate isotridecyl (Crodamol TN (J) (ES02976) from CRODA)) 9,000 - Polyglycerol isso-stearate (4 moles) (Isolan GI 34 from GOLDSCHMIDT 1,500 DEGUSSA) A2 -Dodecandiol ethers (2.2 moles) and polyethylene glycol (45 0E) (Elfacos ST 9 from AKZO NOBEL) 4,000 A3 - Cyclopentadimethylsiloxane (DOW CORNING 245 DOW CORNING fluid) 28,625 - Mixture of polydimethylsiloxane oxyethyloxypropylene (18 EO / 18OOP), Cyclopentadimethylsiloxane and water (10/88/2 ) (DOW CORNING 5225C DOW CORNING AID formulation) 2,000 A4 - Silica Micro-beads (SB15) MIYOSHI KASEI) 9,000 - Hydrophobic fumed silica (Aerosil R 972 from LCW (SENSIENT)) 0.500 - Hollow microspheres of poly methyl methacrylate (particle size: 10 to 12 microns) (Covabead LH 85 from LCW (SENSIENT)) 3,000 B1 - Water 23,125 Methyl (NIPA) -P-hydroxybenzoate 0.400 - Chlorphenesin (from DENK (MERCK)) 0.300 - Phenoxy-2 ethanol (from SEPPIC) 0.500 - Magnesium sulphate, 7 H2O (from MERCK) 1,000 - Glycerol ( Croderol GV 9000) (from CRODA) 5,000 - 1,3-butylene glycol 3,000 B2 - Water 3,000 - Di-sodium salt of tartrazine (CI: 19140) (LCW 08005 FD and C Yellow 5 (SENSIENT)) 0.255 -Sel di -Sodic bright yellow FCF (CI: 15985) (UNIVAR 37001 FD & Yellow N) 0.302 - Bright green di-sodium salt FCF (CI: 42053) (06503 FD & Green 3 from LCW (SENSIENT)) 0.035 - Salt di-sodium of acid fuchsin D (CI: 17200) (K7057 D and C Red 33) (LCW (SENSIENT) 0,158 Procedure: The Al phase is weighed in a skillet and melted until the clarity of the mel angel. This is stirred in the turbine and the temperature of the oil bath is lowered to about 80 C. The A2 phase is added.

  The pigments of phase A3 are wetted with the oils and then milled with the three-roll mill in three passes. The ground material is incorporated with stirring in the mixture (Al + A2) slightly cooled (temperature below 80 C). The pigment paste is left stirring for about 30 minutes. When the mixture (Al + A2 + A3) is stabilized at a temperature of 68 ° C., the phases A4 and then A5 are introduced. The mechanical homogenization is maintained for 10 minutes. In parallel, the aqueous phase B is prepared in a 400 ml beaker at a temperature of 68 ° C. The emulsion is carried out at 67 ° C. with stirring by slowly pouring the aqueous phase into the fatty phase. Stirring is maintained for 10 minutes. The emulsion is then poured at 68 ° C. and then put in an oven at 20 ° C. for 24 hours.

  This product makes it possible to obtain on a dark skin a neutral brown hue. EXAMPLE 5 Cosmetic Composition of the Water-in-Oil Emulsion Type A-Polydimethylsiloxane Oxypropylene Oxypropylene Blend (18 EO / 18 OP), Cyclopentadimethylsiloxane and Water (10/88/2) (DOW CORNING 5225C DOW CORNING FORMULATION AID) 10,000 - Cyclopentadimethylsiloxane (DOW CORNING 245 DOW CORNING fluid) 12,500 B - Sodium Chloride 2,000 Water 36,500 C - Sorghum extract 10,000 - Propylene glycol (MONOPROPYLENE GLYCOL CODEX from INNOVENE) 14,000 - Dipropylene Glycol (DIPROPYLENE GLYCOL from INNOVENE) 10,000 20 D - Ethanol 5,000

  Procedure: The emulsion is cold. Phase A is weighed into a 400 ml beaker and then stirred with Moritz. Phases B, C and D are weighed separately. The emulsion is carried out at room temperature by slowly pouring the aqueous phase B into the fatty phase A and increasing the stirring. Stirring is maintained for 10 minutes, and phase C is added (stirring for 5 minutes) followed by phase D (stirring for 10 minutes). This product makes it possible to obtain on a dark skin a red brown hue. The measured hiding power (Contrast Ratio) with this staining base is 8.82 and its viscosity is 1950 centipoise.

Claims (20)

  A method of making a dark skin comprising applying to said skin a composition comprising in a physiologically acceptable medium at least one direct coloring system in the soluble state, said composition also having a viscosity greater than 100. centipoise and a hiding power, defined by the Contrast Ratio, less than 80.   2. Dark-skin makeup process comprising the application to said skin of a composition comprising in a physiologically acceptable medium at least one direct coloring system in the soluble state, said composition having a hiding power, defined by the Contrast Ratio, less than 80 and a pH greater than 5.   3. Method according to any one of the preceding claims, wherein the composition has a viscosity greater than 100 centipoise, especially greater than 300 centipoise.   4. Method according to any one of the preceding claims, wherein said composition has a hiding power, defined by the Contrast Ratio, less than 80, in particular less than or equal to 50.   5. Method according to any one of the preceding claims wherein the direct dyeing system is formed of water soluble (s), or liposoluble (s) dyeing agent (s) or a mixture thereof.   6. Method according to any one of claims 1 to 5, wherein said direct dyeing system comprises at least one dye selected from DC Red 17, DC Red 21, DC Red 27, DC Green 6, DC Yellow 11, DC Violet 2, DC Orange 5, Sudan Red, Carotenes, Xanthophylls, Palm Oil, Sudan Brown, Quinoline Yellow, Annatto, Curcumin, FDC Red 4, DC Red 6, DC Red 22, DC Red 28, DC Red 30, DC Red 33, DC Orange 4, DC Yellow 5, DC Yellow 6, DC Yellow 8, FDC Green 3, DC Green 5, FDC Blue 1, betamine, carmine, cupric chlorophyllin, methylene blue, anthocyanins, riboflavin, juglone, lawsone, caramel, fermented soybean extracts, seaweed, mushrooms , microorganisms, unsubstituted Flavylium salts at position 3, extracts of Gesneria Fulgens, Blechum Procerum, Saxifraga and pigments likely to be obtained by extraction with a soil organic or hydro-organic medium of a monascus monascus micromycetes culture medium.   The method of any one of the preceding claims, wherein said direct dyeing system comprises at least one natural coloring agent.   8. Process according to any one of the preceding claims, in which the composition comprises from 0.001 to 5%, especially from 0.01 to 3% and in particular from 0.025 to 1% by weight of coloring agent (s) forming the direct color system.   9. Method according to any one of the preceding claims, characterized in that said composition provides a variation of negative clarity AL ranging from -20 to -1 and a saturation variation AC * ranging from 0.5 to 20.   The method of any one of the preceding claims, wherein said composition comprises at least one fatty phase.   11. A process according to any one of the preceding claims, wherein said composition comprises at least one aqueous phase.   The process of any one of claims 1 to 10, wherein said composition is anhydrous.   13. The method according to claim 10, 11 or 12, wherein said fatty phase contains at least one fatty substance that is liquid at ambient temperature and at atmospheric pressure and / or at least one fatty substance that is solid at ambient temperature and at atmospheric pressure.   14. The method of claim 13, wherein said fat body liquid at room temperature and at atmospheric pressure comprises at least one volatile or non-volatile oil or a mixture thereof. 25   15. The method of claim 13 or 14, wherein said solid body at room temperature and atmospheric pressure is selected from waxes, pasty fatty substances, gums and mixtures thereof.   The process of any of the preceding claims, wherein said composition comprises less than 15% by weight filler (s). 30   17. A method according to any one of the preceding claims, wherein said composition further comprises at least pigments and / or nacres in the dispersed state.   18. A method according to any one of the preceding claims, wherein said composition is in a fluid form of liquid type, paste, direct or inverse emulsion, or gel.   19. The process as claimed in any one of claims 1 to 17, wherein said composition is in a solid form, in particular a compact, pulverulent or cast form or in the form of a stick.   20. A method according to any one of the preceding claims, wherein said composition is in the form of a foundation to be applied to the face or neck, a concealer, a concealer complexion , a tinted cream, or a facial makeup base or a body makeup composition.