• 专利附录
  • 专利说明
  • 权利要求
  • 类似技术
  • 同族专利
  • 引用文献
  • 法律状态
  • 优先权
    • 专利摘要:
    Process for improving the sensory and / or aesthetic properties of an oil-in-water topical emulsion (E0), characterized in that an effective amount of a hydrocarbon mixture (M1) is incorporated therein saturated cyclic or acyclic, linear or branched of which at least 95% by weight comprise from fifteen to nineteen carbon atoms; new solar emulsion its use as skin protector.
    公开号:FR3060322A1
    申请号:FR1662650
    申请日:2016-12-16
    公开日:2018-06-22
    发明作者:Sophie Cambos；Florence Clemenceau；Emmanuelle Merat；Cecile Taillebois；Sabrina Mizael；Corinne Stoltz；Nelly Michel；Benjamin Swoboda
    申请人:Societe dExploitation de Produits pour les Industries Chimiques SEPPIC SA；Total Marketing Services SA；
    IPC主号:
    专利说明:

    Holder (s): COMPANY OF OPERATION OF PRODUCTS FOR THE CHEMICAL INDUSTRIES SEPPIC Limited company, TOTAL MARKETING SERVICES Limited company.
    Extension request (s)
    Agent (s): AIR LIQUIDE.
    54) PROCESS FOR IMPROVING SENSORY PROPERTIES OF OIL-IN-WATER EMULSIONS.
    (5 /) Process for improving the sensory and / or aesthetic properties of an emulsion for topical use (E o ) of the oil-in-water type, characterized in that an effective amount of a mixture is incorporated therein ( M ·,) of cyclic or acyclic, linear or branched saturated hydrocarbons of which at least 95% by mass contain from fifteen to nineteen carbon atoms; new solar emulsion its use as a skin protector.
    FR 3 060 322 - A1
    The subject of the invention is a new process for improving the sensory and aesthetic properties of an oil-in-water type emulsion on human skin.
    A large number of cosmetic formulations for topical application are intended to protect the skin, the mucous membranes and the scalp, from external and environmental aggressions and stresses. For example, the consumer is looking for formulations to be applied to the skin which will protect it from the harmful and unsightly effects of prolonged exposure to ultraviolet radiation from the sun, or which will prevent against alterations to the integrity of his skin following an increasingly frequent exposure to pollutants present in atmospheres, and more particularly urban atmospheres.
    To meet these demands aimed at maintaining and / or restoring the integrity of the skin in the face of identified external elements or natural aging, the cosmetics and dermocosmetics industries have developed new specific ingredients in recent decades to improve the performance required by consumers.
    On the other hand, the consumer is also awaiting the sensory and aesthetic properties provided by the cosmetic and dermocosmetic compositions, which gives him both feelings of well-being during and after application to the skin, and also an identification with an external aspect of the cosmetic or dermocosmetic formulation, referring to a quality criterion. Thus, consumers are looking for cosmetic or dermocosmetic compositions whose strong consistency which is called "richness" is often associated with a feeling of skin comfort during and after application to the skin. This feeling of comfort is reinforced when the step of spreading the cosmetic or dermo-cosmetic composition is easy, namely when its duration is reduced or more precisely is not prolonged following resistances on the skin during said spreading and / or when the consumer has to apply a high shearing force to the skin, also resulting in a higher speed of application to spreading and / or by the application of a force of higher intensity during the said spreading phase.
    In specific cases, such as for example those of cosmetic or dermocosmetic formulations intended for the prevention against the undesired effects (rednesses, erythemas and burns) of the ultraviolet rays of the sun on the skin or those of the creams intended for the anti-inflammatory treatments and anti-rheumatic drugs by the local route, comprising for example ibuprofen, camphor, diclofenac or clove essences, which are characterized by implementation difficulties during spreading, it has been observed that consumers are less rigorous in the implementation of the procedures for applying said protection or care products. They therefore often apply too little product and / or at a frequency that is not sustained enough and this results in less protection of the skin than that provided for in the instructions and / or on the packaging.
    Thus, to encourage better and more frequent application of these formulations for the prevention and protection of the skin, it is important that said formulations have pleasant sensory properties and can spread over the skin in a homogeneous, rapid manner and without involving too high an application intensity.
    On the other hand, consumers are looking for cosmetic or dermocosmetic formulations which do not alter the external appearance of the skin, for example by leaving an oily residue in the form of a light film and, conversely, a cosmetic or dermocosmetic formulation giving a matte appearance to the skin will be preferred and sought after.
    Finally, the external appearance of the cosmetic or dermocosmetic formulation can constitute a proven choice and attraction criterion for its use by the consumer. Thus, a cosmetic or dermocosmetic formulation having a heterogeneous external appearance, revealing a slight layer of yellowish oil on the surface after storage will not be considered attractive whereas, on the contrary, a homogeneous cosmetic or dermocosmetic formulation after prolonged storage and having an appearance shiny will be considered attractive because it reflects a quality exterior image.
    Taking into account all these requirements, the person skilled in the art can only note that a large number of protection and care products, such as for example sun protection products or topical treatment of inflammations, which show great effectiveness, cause however, greasy and unpleasant sensations when they are spread over the skin, said spreading having to be carried out over a relatively long period and requiring a more intense speed of application.
    These protection and care formulations can be in the form of an oil-in-water type emulsion in order to be able to provide a more pleasant sensation by bringing an aqueous phase into contact with the skin, but the surface-active or polymeric emulsifying agents. necessary to maintain the stability of said oil-in-water emulsion can also contribute to discomfort during application by imparting a feeling of heaviness to the emulsion during and after its application to the skin.
    An alternative may consist in the development of an emulsion of the water-in-oil type, which is stabilized by thickening of the oily phase by the use in particular of waxes and linear fatty alcohols whose hydrocarbon chain comprises from 14 to 22 carbon atoms. Silicone elastomers are also used to stabilize such a water-in-oil type emulsion, but said silicone elastomers also involve a deterioration of the sensory properties of the skin thus treated by the application of said emulsion. In addition, the use of these silicone elastomers as stabilizers for water-in-oil sun emulsions modifies in certain cases the solubility of the sunscreens used which can then precipitate in the bottle during storage.
    To avoid being confronted with the drawbacks mentioned above both for water-in-oil type emulsions and for oil-in-water type emulsions, the formulator must develop an emulsion having improved spreading properties , then allowing the consumer to apply the emulsion to his skin, without being confronted with frictional forces contrary to the movement established by the applicator and then slows down said application and / or requires a spreading speed more important.
    European patent application published under the number EP 2 644 188 A1 of oil-in-water type emulsions having improved spreading properties on the skin comprising a combination of at least one crosslinked and non-emulsifying silicone resin, minus a polyvinyl alcohol, a thickener of the polyacrylamide type, an oil chosen from the group consisting of vegetable oils of the triglyceride type, waxes, ethoxylated fatty alcohols, fatty acid esters, fatty acids, fatty alcohols , silicone oils and perfluorinated oils.
    2 The international application published under the number WO 2011/065771 discloses and teaches that the spreading and the softness obtained during the application of a water-in-oil-in-water emulsion, prepared from a water-in-oil type emulsion comprising an emulsifier based on silicone, emulsifier of di-polyhydroxyalkylate type, a mineral thickener of hectorite type, and a polar oil.
    These solutions of the state of the art describe an improvement in the spreading properties of an emulsion by using silicone compounds and other surfactants for which those skilled in the art are looking for an alternative in an approach that takes into account. of sustainable development, and more particularly in an approach of using ingredients that do not emit and / or the manufacture of which does not involve volatile organic compounds (VOC) and / or the use of biodegradable ingredients according to standards current regulations and / or use ingredients of plant origin and no longer fossil.
    Some of the desired aesthetic properties, such as for example those intended to impart a matte appearance to the skin, are achieved by the use in the cosmetic formulation of polymers considered to be plastics and therefore for which an alternative to obtaining a matt effect on the skin is sought.
    More specifically, silicone derivatives, such as chemical substances and compositions from the polysiloxane family, are known to provide improved sensory properties to oil-in-water emulsions and in particular in terms of ease of spreading and limitation of residues. lipids on the skin after application. However, the environmental characteristics associated with these ingredients have necessitated the search for substitutes which provide similar sensory properties while having environmental characteristics in accordance with the regulations in force and to come, and in conformity with the requirements of the consumers in the matter. A partially satisfactory alternative has been demonstrated, by the use of alkane compositions comprising large amounts of cyclo-alkanes to prepare cosmetic emulsions in water; said mixtures of alkanes having satisfactory properties of biodegradability and satisfactory sensory properties but considered to be perfectible.
    Consequently, there is a need to develop cosmetic or dermocosmetic formulations which have improved sensory properties, in particular which provide a feeling of richness and which is easy to spread on the skin, and which have improved aesthetic characteristics and / or attractive, for example, characterized by an improved shiny appearance and giving the skin a mat and non-shiny appearance.
    The inventors therefore sought to develop a new solution for improving the sensory and aesthetic properties of an oil-in-water type emulsion for topical use, not necessarily employing silicone derivatives, but using chemical compositions of vegetable and / or biodegradable origins.
    This is why, according to a first aspect, the subject of the invention is a method for improving the sensory and / or aesthetic properties of an emulsion (E o ) of the oil-in-water type, characterized in that one incorporates into said oil-in-water type emulsion (E o ), an effective amount of a mixture (IVf) of cyclic or acyclic, linear or branched saturated hydrocarbons of which at least 95% by mass contains from fifteen to nineteen carbon atoms.
    By “sensory properties” of an (E o ) oil-in-water, we mean, within the meaning of the present invention, the sensations experienced and observed by a user who applies the oil type emulsion (E) to the skin. in water resulting from said process above: and which correspond to physico-chemical and / or rheological characteristics of said emulsion (E).
    By "aesthetic properties" is meant in the sense of the present invention visual characteristics associated with the emulsion for use (E) oil-in-water as such and also associated with the condition of the skin after application of said emulsion for topical use (E) oil-in-water.
    By effective quantity, we mean, in the definition of the process as defined above, a quantity such that the emulsion for topical use (E) of oil-in-water type resulting from said process above: shows an average value d '' at least three measurements of the variation in the friction coefficient, as a function of the application velocity between 1 radian.s ' 1 and 4 radian.s' 1 , less than or equal to 10% of the value initially measured for a application velocity on the skin equal to 1 radian.s'1; said coefficients of friction being recorded during each of the measurements by means of a DHR2 rheometer (TA Instrument) equipped with a Peltier plane type support on which a plexiglass surface is placed on which the emulsion to be tested is deposited .
    By emulsion (E o ) of the oil-in-water type, the meaning of the present invention is emulsions comprising for 100% by mass:
    - from 95% to 50%, more particularly from 90% to 70% of a cosmetically acceptable aqueous phase (A o ),
    - from 5% to 50%, more particularly from 10% to 30% of an fatty phase (G o ), said fatty phase (G o ) comprising for 100% of its mass, from 1% to 12%, more particularly from 2% to 8% of at least one oil-in-water type surfactant and from 88% to 99%, more particularly from 92% to 98% of at least one oil and / or a wax.
    By “oil” present in the fatty phase (G o ) of the emulsion (E o ) of the oil-in-water type as defined above, is meant within the meaning of the present invention the chemical substances or mixtures of chemical substances insoluble in water, and having a liquid appearance at a temperature of 25 ° C.
    By “wax” present in the fatty phase (G o ) of the oil-in water type emulsion (E o ) as defined above, is meant within the meaning of the present invention the chemical substances or mixtures of chemical substances insoluble in water, and having a solid appearance at a temperature of 45 ° C.
    By “oil-in-water type surfactant” present in the fatty phase (G o ) of the topical oil-in-water emulsion (E o ) as defined above, is meant in the sense of the present invention , the chemical substance or the mixture of chemical substances which makes it possible to stabilize the droplets of said fatty phase (G o ) in dispersion in the continuous phase (A o ).
    As oil-in-water type surfactant present in the fatty phase (G °) of the oil-in-water type emulsion (E o ) as defined above, there may be mentioned for example:
    - Polysorbates resulting from the ethoxylation reaction between a molar equivalent of sorbitan esters and between 5 and 20 molar equivalents of ethylene oxide, and more particularly between a molar equivalent of sorbitan laurate, or of sorbitan palmitate , or sorbitan stearate, or sorbitan isostearate, or sorbitan oleate, and between 5 and 20 molar equivalents of ethylene oxide;
    - The products resulting from the ethoxylation reaction between a molar equivalent of a fatty acid, such as for example palmitic acid, myristic acid, lauric acid, stearic acid, isostearic acid, oleic acid, and between 5 to 40 molar equivalents of ethylene oxide;
    - The products resulting from the esterification reaction between a fatty acid, such as for example palmitic acid, myristic acid, lauric acid, stearic acid, isostearic acid, oleic acid, arachidic acid, behenic acid and between 4 to 20 molar equivalents, more particularly between 3 to 10 molar equivalents of glycerol;
    The cosmetically acceptable expression used in the definition of the aqueous phase (A o ) of the oil-in-water emulsion, means, according to the directive of the Council of the European Economic Community N ° 76/768 / EEC of 27 July 1976 modified by Directive No. 93/35 / EEC of June 14, 1993, any substance or preparation intended to be in contact with the various parts of the human body (epidermis, hair and capillary system, nails, lips and genitals) or with teeth and oral mucosa exclusively and mainly for cleaning, perfuming, modifying their appearance and / or correcting body odors and / or protecting or maintaining them in good condition. A cosmetically acceptable medium of these compositions which are the subject of the invention may conventionally contain water, one or more cosmetically acceptable organic solvents, a mixture of water and one or more organic solvents. The cosmetically acceptable solvents can more particularly be chosen from polyhydric alcohols such as for example glycerol, diglycerol, glycerol oligomers, ethylene glycol, propylene glycol, hexylene glycol, diethylene glycol, xylitol, erythritol, sorbitol, or water-soluble alcohols.
    According to a particular mode of the process as defined above, by effective quantity of said mixture (IVf), a mass proportion of 1% to 25% of the oil-in-water emulsion is designated, very particularly from 5% to 20%.
    The expression for topical use used in the definition of the process as defined above, means that the said composition is applied by application to the skin, the hair, the scalp or the mucous membranes, whether it is a direct application in the case of a cosmetic, dermocosmetic, dermopharmaceutical or pharmaceutical composition or of an indirect application for example in the case of a body hygiene product in the form of a textile or paper wipe or of sanitary products intended for be in contact with the skin or mucous membranes.
    By “linear alkanes” present in the mixture (IVf) used in the process which is the subject of the present invention, and comprising from fifteen to nineteen carbon atoms, are denoted more particularly within the meaning of the present invention the elements chosen from the group consisting of pentadecane, hexadecane, heptadecane, octadecane and nonadecane.
    By “branched alkanes” present in the mixture (IVf) used in the process which is the subject of the present invention, and comprising from fifteen to nineteen carbon atoms, is meant more particularly within the meaning of the present invention the elements chosen from the group consisting of 2-methyl tetradecane (or isopentadecane), 2methyl pentadecane (or isohexadecane), 2-methyl hexadecane (or isoheptadecane), 2methyl heptadecane (or isooctadecane) and 2-methyl octadecane (or isononecane).
    By cyclo-alkanes present in the mixture (IVf) used in the process which is the subject of the present invention, and comprising from 15 to 19 carbon atoms, is meant more particularly within the meaning of the present invention saturated hydrocarbons comprising at least one saturated cyclic hydrocarbon group optionally substituted by one or more linear or branched alkyl radicals.
    According to a particular aspect, the invention relates to a process as defined above, characterized in that said mixture (IVf) comprises per 100% of its mass:
    - A proportion by mass of branched alkanes greater than or equal to 80% and less than or equal to 100%, and more particularly greater than or equal to 90% by mass;
    - A mass proportion of linear alkanes greater than or equal to 0% and less than or equal to 15%, and more particularly less than or equal to 10% by mass;
    - A mass proportion of cyclo-alkanes greater than or equal to 0% and less than or equal to 5%, and more particularly less than or equal to 1% by mass, and in that from 95% by mass to 100% by mass of said cyclic or acyclic hydrocarbons , linear or branched, contain from fifteen to nineteen carbon atoms and in that up to 5% by mass of said cyclic, acyclic, linear or branched hydrocarbons contain less than fifteen carbon atoms or more than nineteen carbon atoms .
    According to a more particular aspect, the invention relates to a process as defined above, in which the mixture (IVf) is a mixture of saturated hydrocarbons marketed under the brand name Emogreen ™ L15 comprising for 100% of its mass:
    i) 3.7% of linear alkanes having from fifteen to nineteen carbon atoms, ii) 96% of iso-alkanes comprising from fifteen to nineteen carbon atoms, and iii) 0.3% of cyclo -alkanes having from fifteen to nineteen carbon atoms.
    According to another more particular aspect, the invention relates to a process as defined above, characterized in that said mixture (MQ comprises per 100% of its mass:
    - A proportion by mass of branched alkanes greater than or equal to 40% and less than or equal to 100%, and more particularly greater than or equal to 50% by mass,
    - A mass proportion of linear alkanes greater than or equal to 0% and less than or equal to 20%, and more particularly less than or equal to 15% by mass
    - A mass proportion of cycloalkanes greater than or equal to 0% and less than or equal to 40% and more particularly less than or equal to 35% by mass, and in that 100% by mass of said cyclic or acyclic hydrocarbons, linear or branched, comprise from fifteen to nineteen carbon atoms.
    According to a very particular aspect, the invention relates to a process as defined above, in which the mixture (IVf) is a mixture of saturated hydrocarbons marketed under the brand name Emosmart ™ L19, comprising for 100% of its mass :
    i) 13.20% by mass of linear alkanes having from 15 to 19 carbon atoms, ii) 55.00% by mass of iso-alkanes having from 15 to 19 carbon atoms, and iii) 31.80% of cyclo -alkanes having from 15 to 19 carbon atoms.
    According to another particular aspect, the invention relates to the process as defined above for which the sensory properties are the spreading properties of said emulsion for topical use (E o ).
    By “spreading properties on the skin”, is meant in the sense of the present invention, the capacity for the oil-in-water emulsion object of the present invention to be spread on the surface of the skin in a thin layer and so as to cover a large area of the skin while remaining sufficiently concentrated to fulfill the mission assigned to it by its composition, such as for example protecting the skin against the consequences of prolonged exposure to ultraviolet radiation from the sun if the oil-in-water emulsion contains organic and / or inorganic sunscreens. The properties of spreading on the skin of an oil-in-water type emulsion, namely the ease or difficulty of spreading on the human skin of said emulsion, can be evaluated by the use of different methods, such as for example the methods allowing the measurement of the values of the flow threshold, and / or the measurement of the rheo-fluidification index, and / or the measurement of the coefficient of friction and / or the measurement of the variation of the coefficient of friction as a function of the speed of said spreading.
    According to another particular aspect, the invention relates to the method as defined above for which the sensory properties are the properties of consistency and richness of said emulsion for topical use (E o ). By richness of said emulsion for topical use (E o ), is meant in the sense of the present invention the sensation provided by the application to the skin of an emulsion for topical use (E o ), as defined above, which characterized by a compact non-fluid or non-flowing consistency if subjected to the sole force of gravity, and a presence of the emulsion during spreading on the skin significantly greater in comparison with the spreading of water; by "presence", the person skilled in the art therefore means a sensory perception devoid of an aqueous character.
    According to another particular aspect, the subject of the invention is the method as defined above for which the aesthetic property is the gloss of the emulsion for topical use (E o ) of the oil-in-water type resulting from said method above. By brightness, is meant in the sense of the present invention, the ability of the emulsion to reflect incident rays from a light source of the visible spectrum with a given reflection efficiency.
    According to another particular aspect, the invention relates to the process as defined above for which the aesthetic property is the matt appearance of the skin observed after the application to the skin of an emulsion for topical use (E o ) of oil-in-water type resulting from said process above. By matt appearance of the skin is meant in the sense of the present invention, the ability of the skin to absorb a given proportion of incident rays coming from a light source of the visible spectrum, said capacity being related to the thickness and the nature of the residual emulsion film remaining on the skin after its application.
    The subject of the invention is also an emulsion of oil-in-water type (E) comprising for 100% of its mass:
    - From 50% to 90% by mass, more particularly from 60% to 90% by mass and even more particularly from 70% to 90% by mass of a cosmetically acceptable aqueous phase (A),
    - From 10% to 50% by mass, more particularly from 10% to 40% by mass and even more particularly from 10% to 30% by mass of an fatty phase (G) comprising for 100% of its mass:
    - From 10% to 50% by mass, more particularly from 15% to 40% by mass of a mixture (MJ of cyclic or acyclic, linear or branched saturated hydrocarbons among which at least 95% by mass comprises from fifteen to nineteen atoms of carbon;
    - From 0.5% to 15% by mass, more particularly from 1% to 10% by mass of at least one surfactant of the oil-in-water type,
    - From 5% to 30% by mass, more particularly from 15% to 30% by mass of at least one agent for protection against ultraviolet radiation from the sun,
    - From 0% to 80% by mass, more particularly from 0% to 60% by mass of at least one oil and / or a wax, it being understood that such an oil and / or such a wax does not meet the definition of said mixture (MJ.
    By fatty phase (G) is meant in the sense of the present invention, a fatty substance or a mixture of fatty substances insoluble in water and / or in mixtures of water and polar solvents. Such a "fatty phase" can include oils and / or waxes.
    Among the constituent elements of the fatty phase, one can cite:
    - Oils of animal origin, such as squalene or squalane;
    - vegetable oils, such as phytosqualane, sweet almond oil, coconut oil, castor oil, jojoba oil, olive oil, rapeseed oil, l peanut oil, sunflower oil, wheat germ oil, corn germ oil, soybean oil, cottonseed oil, alfalfa oil, poppy, pumpkin oil, evening primrose oil, millet oil, barley oil, rye oil, safflower oil, bancoulier oil, passionflower, hazelnut oil, palm oil, shea butter, apricot kernel oil, calophyllum oil, sysymbrium oil, avocado oil, oil calendula, sesame oil, meadowsweet oil, Macadamia kiwi oil, borage oil, blackcurrant seed oil, coffee oil, pistachio oil, peach kernel oil, raspberry seed oil, strawberry seed oil, melon oil, blueberry seed oil, argan oil, e x oily extract of plum, pomegranate oil, papaya oil, coconut milk oil, oils from flowers or vegetables;
    - Ethoxylated vegetable oils;
    - Synthetic oils such as fatty acid esters such as butyl myristate, propyl myristate, cetyl myristate, isopropyl palmitate, butyl stearate, hexadecyl stearate, isopropyl stearate , octyl stearate, isocetyl stearate, dodecyl oleate, hexyl laurate, propylene glycol dicaprylate, esters derived from lanolic acid, such as isopropyl lanolate, isocetyl lanolate , monoglycerides, diglycerides and triglycerides of fatty acids such as glycerol triheptanoate, alkylbenzoates, hydrogenated oils, polyalphaolefins, polyolefins such as polyisobutene, hydrogenated polydecene or hydrogenated polyisobutene, marketed in France by the company Ets B. Rossow et Cie under the name PARLEAM POLYSYNLANE ™, cited in: Michel and Irene Ash; Thesaurus of Chemical Products, Chemical Publishing Co, Inc. 1986 Volume I, page 211 (ISBN 0 7131 3603 0);
    - Silicone oils such as dimethylpolysiloxanes, methylphenylpolysiloxanes, silicones modified by amines, silicones modified by fatty acids, silicones modified by alcohols, silicones modified by alcohols and fatty acids, silicones modified by polyether groups, modified epoxy silicones, silicones modified by fluorinated groups, cyclic silicones and silicones modified by alkyl groups.
    - Waxes like beeswax, carnauba wax, candelilla wax, ouricoury wax, Japanese wax, cork fiber wax, sugar cane wax, jojoba wax, blackcurrant flower wax, narcissus flower wax, orange blossom wax, orange wax, rice wax, paraffin waxes, lignite waxes, microcrystalline waxes, dewax lanolin; ozokerite; polyethylene wax, silicone waxes; vegetable waxes; fatty alcohols and fatty acids solid at room temperature; solid glycerides at room temperature.
    By “oil-in-water type surfactant” present in the fatty phase (G) of the oil-in-water type emulsion (E) as defined above, a chemical substance or the mixture of chemical substance which allows stabilize the droplets of the fatty phase (G) dispersed in the continuous phase (A). We can quote for example:
    - Polysorbates resulting from the ethoxylation reaction between a molar equivalent of sorbitan esters and between 5 and 20 molar equivalents of ethylene oxide, and more particularly between a molar equivalent of sorbitan laurate, or of sorbitan palmitate , or sorbitan stearate, or sorbitan isostearate, or sorbitan oleate, and between 5 and 20 molar equivalents of ethylene oxide;
    - The products resulting from the ethoxylation reaction between a molar equivalent of a fatty acid, such as for example palmitic acid, myristic acid, lauric acid, stearic acid, isostearic acid, oleic acid, and between 5 to 40 molar equivalents of ethylene oxide;
    - The products resulting from the esterification reaction between a fatty acid, such as for example palmitic acid, myristic acid, lauric acid, stearic acid, isostearic acid, oleic acid, arachidic acid, behenic acid and between 4 to 20 molar equivalents, more particularly between 3 to 10 molar equivalents of glycerol;
    A cosmetically acceptable aqueous phase (A) included in the oil-in-water emulsion (E) as defined above may conventionally contain one or more cosmetically acceptable organic solvents, a mixture of water and one or more cosmetically acceptable organic solvents. The cosmetically acceptable solvents can more particularly be chosen from polyhydric alcohols such as for example glycerol, diglycerol, triglycerol, glycerol oligomers, xylitol, erythritol, sorbitol, methyl-2-propanediol-1,3 ; alkoxylated polyhydric alcohols; glycols, such as butylene glycol, hexylene glycol, caprylyl glycol or 1,2octanediol, pentylene glycol or 1,2-pentanediol, monopropylene glycol, dipropylene glycol, isoprene glycol, butyldiglycol, polyethylene glycols whose molecular weight is between 200g.mol-1 and 8000g.mol-1; or water-soluble alcohols such as, for example, ethanol, isopropanol or butanol.
    By agent for protection against ultraviolet radiation from the sun, is meant in particular in the definition of the oil-in-water type emulsion (E) which is the subject of this patent application, pigments, organic solar filters and filters. inorganic solar.
    As pigments used as a protective agent against ultraviolet radiation from the sun, there are for example titanium dioxide, brown iron oxides, yellow iron oxides, black iron oxides, or red iron oxides or else white or colored pearlescent pigments such as Mica-Titanium.
    As organic sun filters used as a protective agent against ultraviolet radiation from the sun, there are for example:
    - Those of the family of benzoic acid derivatives such as paraaminobenzoic acids (PABA), in particular the monoglycerol esters of PABA, the ethyl esters of Ν, Ν-propoxy PABA, the ethyl esters of Ν, Ν-diethoxy PABA, Ν, Ν-dimethyl PABA ethyl esters, Ν, Ν-dimethyl PABA methyl esters, Ν, Ν-dimethyl PABA butyl esters;
    - Those of the family of anthranilic acid derivatives such as homomenthyl-Nacetyl anthranilate;
    - Those of the family of salicylic acid derivatives such as amyl salicylate, homomenthyl salicylate, ethylhexyl salicylate, phenyl salicylate, benzyl salicylate, p-isopropanolphenyl salicylate;
    - Those of the family of cinnamic acid derivatives such as ethylhexyl cinnamate, ethyl-4-isopropyl cinnamate, methyl-2,5-diisopropyl cinnamate, p-methoxypropyl cinnamate, cinnamate of p-methoxyisopropyl, pmethoxyisoamyl cinnamate, p-methoxyoctyl cinnamate (p-methoxy 2ethylhexyl cinnamate), p-methoxy 2-ethoxyethyl cinnamate, pmethoxycyclohexyl cinnamate, ethyl-a-cyano cinnamate p-phenyl, 2-ethylhexyl cinnamate □ a-cyano-p-phenyl, glyceryl diparamethoxy cinnamate mono-2-ethylhexanoyl;
    - Those of the family of benzophenone derivatives such as 2,4-dihydroxy benzophenone, 2,2'-dihydroxy 4-methoxy benzophenone, 2,2 ', 4,4'-tetrahydroxy benzophenone, 2-hydroxy 4 -methoxy benzophenone, 2-hydroxy 4-methoxy 4'-methyl benzophenone, 2-hydroxy 4-methoxy benzophenone-5-sulfonate, 4-phenyl benzophenone, 2-ethylhexyl 4'-phenyl benzophenone-2-carboxylate, 2-hydroxy 4-noctyloxy benzophenone, 4-hydroxy 3-carboxy benzophenone; 3- (4'-methylbenzylidene) d, l-camphor, 3- (benzylidene) -d, l-camphor, benzalkonium methosulfate camphor; urocanic acid, ethyl urocanate;
    -These from the family of derivatives of sulfonic acid such as 2-phenyl benzimidazole-5-sulfonic acid and its salts; the family of triazine derivatives such as hydroxyphenyl triazine, ethylhexyloxyhydroxyphenyl-4-methoxyphenyltriazine, 2,4,6trianillino- (p-carbo-2'-ethylhexyl-1'-oxy) 1,3,5-triazine , 4,4 - ((6 - (((1,1-dimethylethyl) amino) carbonyl) phenyl) amino) -1,3,5-triazine-2,4-diyl diimino) bis- (2-ethylhexyl) benzoic acid ester, 2-phenyl-5-methyl benzoxazole, 2,2'-hydroxy-5-methylphenyl benzotriazole, 2- (2'-hydroxy-5'-t-octylphenyl) benzotriazole, 2 - (2'-hydroxy-5'-methyphenyl) benzotriazole; dibenzazine; dianisoylmethane, 4-methoxy-4-t-butylbenzoylmethane; 5- (3,3-dimethyl-2-norbornylidene) -3-pentan-2-one; 2- (4-diethylamino 2-hydroxy benzoyl) benzoic acid hexyl ester, 2,4-bis {[4- (2-ethylhexyloxy) -2-hydroxy] phenyl} -6- (4methoxy phenyl) 1,3, 5-triazine, 2,4,6-tris [4- (2-ethylhexyloxycarbonyl) anilino] -1,3,53060322 triazine, 2-ethylhexyl dimethoxybenzylidene dioxoimidazolidine propionate, the family of diphenylacrylate derivatives such as 2-ethylhexyl- 2-cyano-3,3-diphenyl-2-propenoate, ethyl-2-cyano-3,3-diphenyl-2-propenoate;
    - Those of the polysiloxane family such as benzylidene siloxane malonate.
    As inorganic solar filters used as a protective agent against ultraviolet radiation from the sun, there are for example: titanium oxides, zinc oxides, cerium oxide, zirconium oxide, iron oxides yellow, red or black, chromium oxides. These mineral screens can be micronized or not, have undergone or not surface treatments and may be presented in the form of aqueous or oily pre-dispersions.
    According to a particular aspect, the subject of the invention is an oil-in-water emulsion for topical use (E) as defined above, in which the agent for protection against ultraviolet radiation from the sun is chosen from the elements of group consisting of titanium dioxide, 2,4-dihydroxy benzophenone, 2- (4-diethylamino-2-hydroxybenzoyl) benzoic acid hexyl ester, 2,4-bis {[4- (2-ethylhexyloxy) -2- hydroxy] phenyl} -6- (4methoxyphenyl) -1,3,5-triazine, 2,4,6-tris [4- (2-ethylhexyloxy carbonyl) anilino] -1,3,5triazine and 2-ethylhexyl dimethoxy benzylidene dioxoimidazolidine propionate.
    According to a particular aspect, the invention relates to an oil-in-water emulsion (E) as defined above, characterized in that said mixture (IVf) comprises per 100% of its mass:
    - A proportion by mass of branched alkanes greater than or equal to 80% and less than or equal to 100%, and more particularly greater than or equal to 90% by mass;
    - A mass proportion of linear alkanes greater than or equal to 0% and less than or equal to 15%, and more particularly less than or equal to 10% by mass,
    A proportion by weight of cycloalkanes greater than or equal to 0% and less than or equal to 5%, and more particularly less than or equal to 1% by mass, in that from 95% by mass to 100% by mass of said cyclic or acyclic hydrocarbons, linear or branched, contain from fifteen to nineteen carbon atoms and in that up to 5% by mass of said cyclic, acyclic, linear or branched hydrocarbons contain less than fifteen carbon atoms or more than nineteen carbon atoms.
    According to this particular aspect, said mixture (Mi) is more particularly a mixture of saturated hydrocarbons marketed under the brand name Emogreen ™ L15 comprising for 100% of its mass:
    i) 3.7% of linear alkanes having from fifteen to nineteen carbon atoms, ii) 96% of iso-alkanes comprising from fifteen to nineteen carbon atoms, and iii) 0.3% of cyclo -alkanes having from fifteen to nineteen carbon atoms.
    According to another more particular aspect, the oil-in-water type emulsion (E) as defined above, is characterized in that said mixture (Mfi comprises for 100% of its mass:
    - A proportion by mass of branched alkanes greater than or equal to 40% and less than or equal to 100%, and more particularly greater than or equal to 50% by mass,
    - A mass proportion of linear alkanes greater than or equal to 0% and less than or equal to 20%, and more particularly less than or equal to 15% by mass
    - A mass proportion of cycloalkanes greater than or equal to 0% and less than or equal to 40% and more particularly less than or equal to 35% by mass, and in that 100% by mass of said cyclic or acyclic hydrocarbons, linear or branched, comprise from fifteen to nineteen carbon atoms.
    According to this particular aspect, the mixture (Mfi is more particularly a mixture of saturated hydrocarbons marketed under the brand name Emosmart ™ L19, comprising for 100% of its mass:
    i) 13.20% by mass of linear alkanes having from 15 to 19 carbon atoms, ii) 55.00% by mass of iso-alkanes having from 15 to 19 carbon atoms, and iii) 31.80% of cyclo -alkanes having from 15 to 19 carbon atoms.
    The emulsion (E) as defined above can comprise one or more adjuvants such as:
    - Thickening or gelling agents, for example polyelectrolyte type polymers, linear or branched or crosslinked, such as the homopolymer of partially or fully salified acrylic acid, the homopolymer of partially or fully salified methacrylic acid, homopolymer of 2-methyl - [(1-oxo-2propenyl) amino] -1-propanesulfonic acid (AMPS) partially or fully salified, copolymers of acrylic acid and AMPS, copolymers of acrylamide and AMPS, copolymers of vinylpyrolidone and AMPS, copolymers of AMPS and (2-hydroxyethyl acrylate), copolymers of AMPS and (2hydroxyethyl) methacrylate, copolymers of AMPS and hydroxyethylacrylamide, copolymers of AMPS and Ν, Ν-dimethyl acrylamide, copolymers of AMPS and tris (hydroxymethyl) acrylamido methane (THAM), copolymers of acid acrylic or meth acrylic and (2-hydroxyethyl acrylate), copolymers of acrylic or methacrylic acid and (2-hydroxy ethyl) methacrylate, copolymers of acrylic or methacrylic acid and hydroxyethylacrylamide, copolymers of acrylic or methacrylic acid and THAM, copolymers of acrylic or methacrylic acid and N, Ndimethyl acrylamide, terpolymers of acrylic or methacrylic acid, AMPS and acrylate of (2 -hydroxy ethyl), terpolymers of acrylic or methacrylic acid, AMPS and (2-hydroxyethyl) methacrylate, terpolymers of acrylic or methacrylic acid, AMPS and THAM, terpolymers acrylic or methacrylic acid, AMPS and Ν, Ν-dimethyl acrylamide, terpolymers of acrylic or methacrylic acid, AMPS and acrylamide, copolymers of acrylic acid or methacrylic acid and alkyl acrylates whose carbon chain comprises between four and thirty carbon atoms and more particularly between ten and thirty carbon atoms, AMPS and alkyl acrylate copolymers whose carbon chain comprises between four and thirty atoms of carbon and more particularly between ten and thirty carbon atoms, the linear, branched or crosslinked terpolymers of at least one monomer having a strong, free, partially salified or fully salified acid function, with at least one neutral monomer, and at least a monomer of formula (VIII):
    CH 2 = C (R'3) -C (= O) - [CH2-CH2-O] n-R ' 4 (VIII) in which R' 3 represents a hydrogen atom or a methyl radical, R ' 4 represents a linear or branched alkyl radical containing from eight to thirty carbon atoms and n represents a number greater than or equal to one and less than or equal to fifty; The polymers of the polyelectrolyte type, linear or branched or crosslinked which can be combined with the oil-in-water emulsion object of the present invention, can be in the form of a solution, an aqueous suspension, d a water-in-oil emulsion, an oil-in-water emulsion, a powder, for example the products sold under the names SIMULGEL ™ EG, SIMULGEL ™ EPG, SEPIGEL ™ 305, SIMULGEL ™ 600, SIMULGEL ™ NS, SIMULGEL ™ INS 100, SIMULGEL ™ FL, SIMULGEL ™ A, SIMULGEL ™ SMS 88, SEPINOV ™ EMT 10, SEPIPLUS ™ 400, SEPIPLUS ™ 265, SEPIPLUS ™ S, SEPIMAX ™ Zen, ARISTOFLEX ™ AVC, ARISTOFLEX ™ AVS, NOVEMER ™ EC-1, NOVEMER ™ EC 2,
    ARISTOFLEX ™ HMB, COSMEDIA ™ SP, FLOCARE ™ ET 25, FLOCARE ™ ET 75,
    FLOCARE ™ ET 26, FLOCARE ™ ET 30, FLOCARE ™ ET 58, FLOCARE ™ PSD 30,
    VISCOLAM ™ AT 64, VISCOLAM ™ AT 100; polysaccharides consisting only of oses, such as glucans or homopolymers of glucose, glucomannoglucans, xyloglycans, galactomannans whose degree of substitution (DS) of Dgalactose units on the main chain of D-mannose is between 0 and 1 , and more particularly between 1 and 0.25, like the galactomannans from cassia gum (DS = 1/5), locust bean gum (DS = 1/4), tara gum (DS = 1 / 3), guar gum (DS = 1/2), fenugreek gum (DS = 1); polysaccharides consisting of derivatives of oses, such as sulphated galactans and more particularly carrageenans and agar, uronanes and more particularly algines, alginates and pectins, heteropolymers of oses and uronic acids and more particularly xanthan gum, gellan gum, arabic gum and karaya gum exudates, glucosaminoglycans; cellulose, cellulose derivatives such as methylcellulose, ethyl cellulose, hydroxypropyl cellulose, silicates, starch, hydrophilic starch derivatives, polyurethanes;
    - Film-forming compounds,
    - Hydrotropic agents,
    - Plasticizing agents,
    - Opacifying and / or pearlescent agents, such as sodium or magnesium palmitate, stearate or hydroxy stearate, ethylene or polyethylene glycol monostearates or distearate, fatty alcohols, homopolymers and copolymers of styrene such as the styrene acrylate copolymer sold under the name MONTOPOL ™ OP1 by the company SEPPIC.
    - Texturing agents such as lauroyl lysine sold under the name AMINOHOPE ™ LL by the company AJINOMOTO, octenyl starch succinate sold under the name DRYFLO ™ by the company NATIONAL STARCH, myristyl polyglucoside sold by SEPPIC under name MONTANOV ™ 14, cellulose fibers, cotton fibers, chitosan fibers, talc, sericite, mica;
    - Superfatting agents,
    - sequestering agents,
    - Chelating agents,
    - Non-ionic surfactants such as the ethoxylated derivatives of fatty alcohols containing from 8 to 12 carbon atoms, the ethoxylated derivatives of fatty acids containing from 8 to 12 carbon atoms; ethoxylated derivatives of fatty esters having from 8 to 12 carbon atoms; ethoxylated derivatives of monoglycerides containing from 8 to 12 carbon atoms; the alkylpolyglycosides of formula (II):
    R 2 -O- (S) y -H (II) in which y represents a decimal number between 1 and 5, S represents the remainder of a reducing sugar and R 2 represents a linear or branched, saturated or unsaturated alkyl radical , having 5 to 16 carbon atoms, preferably 8 to 14 carbon atoms, or a mixture of compounds of formula (II), for example caprylyl capryl glucosides, sold in particular under the brand name ORAMIX ™ CG 110, decylglucoside, sold in particular under the brand name ORAMIX ™ NS 10;
    - Antioxidant agents, such as EDTA and its salts, citric acid, tartaric acid, oxalic acid, BHA (butylhydroxyanisol), BHT (butylhydroxytoluene), tocopherol derivatives such as acetate tocopherol, mixtures of antioxidant compounds such as DISSOLVINE GL 47S (INCI name: Tetrasodium Glutamate Diacetate);
    - Perfumes,
    - Preservatives,
    - Conditioners,
    - Active ingredients intended to provide a treating action with respect to the skin or the hair, such as vitamins and their derivatives, in particular their esters, such as retinol (vitamin A) and its esters (retinyl palmitate for example) , ascorbic acid (vitamin C) and its esters, the sugar derivatives of ascorbic acid (such as ascorbyl glucoside), tocopherol (vitamin E) and its esters (such as tocopherol acetate), vitamins B3 or B10 (niacinamide and its derivatives); compounds showing a soothing action, in particular SEPICALM ™ S, allantoin and bisabolol; anti-inflammatory agents; compounds showing a hydrating action such as urea, hydroxyureas, glycerolglucoside, diglycerolglucoside, polyglycerylglucosides; plant extracts rich in polyphenols such as grape extracts, pine extracts, wine extracts, olive extracts; compounds showing a slimming or lipolytic action such as caffeine or its derivatives, ADIPOSLIM ™, ADIPOLESS ™, fucoxanthin; N-acylated proteins; N-acylated peptides such as MATRIXIL ™; N-acylated amino acids; partial hydrolysates of N-acylated proteins; amino acids; peptides; total protein hydrolysates; soy extracts, for example Raffermine ™; wheat extracts, for example TENSINE ™ or GLIADINE ™; plant extracts, such as plant extracts rich in tannins, plant extracts rich in isoflavones or plant extracts rich in terpenes; extracts of freshwater or marine algae; extracts of marine plants; marine extracts in general such as corals; essential waxes; bacterial extracts; ceramides; phospholipids; compounds showing an antimicrobial action or a purifying action, such as LIPACIDE ™ C8G, LIPACIDE ™ UG, SEPICONTROL ™ A5; OCTOPIROX ™ or SENSIVA ™ SC50; compounds showing an energizing or stimulating property such as PHYSIOGENYL ™, panthenol and its derivatives such as SEPICAP ™ MP; antiaging active ingredients like SEPILIFT ™ DPHP, LIPACIDE ™ PVB, SEPMNOL ™, SEPMTAL ™, MANOLIVA ™, PHYTO-AGE ™, TIMECODE ™; SURVICODE ™; anti-photo aging active ingredients; protective agents for the integrity of the dermo-epidermal junction; active ingredients increasing the synthesis of components of the extracellular matrix such as collagen, elastins, glycosaminoglycans; active agents favorably acting on chemical cellular communication such as cytokines or physical ones such as integrins; active ingredients that create a feeling of "warming" on the skin, such as activators of skin microcirculation (such as nicotinic acid derivatives) or products that create a feeling of "freshness" on the skin (such as menthol and derivatives) ; active ingredients improving skin microcirculation, for example veinotonics; draining active ingredients; decongestant active ingredients such as extracts of ginko biloba, ivy, horse chestnut, bamboo, ruscus, small holly, centalla asiatica, fucus, rosemary, willow; agents for tanning or browning the skin, such as for example dihydroxyacetone (DHA), erythrulose, mesotartaric aldehyde, glutaraldehyde, glyceraldehyde, alloxane, ninhydrin, plant extracts such as, for example, extracts red woods of the genus Pterocarpus and of the genus Baphia such as Pteropcarpus santalinus, Pterocarpus osun, Pterocarpus soyauxii, Pterocarpus erinaceus, Pterocarpus indicus or Baphia nitida as those described in European patent application EP 0 971 683 ;; agents known for their facilitating and / or accelerating action on the tanning and / or browning of human skin, and / or for their coloring action on human skin, such as, for example, caratenoids (and more particularly beta carotene and gamma carotene), the product marketed under the brand name "Carrot oil" (INCI name: Daucus Carota, helianthus annuus Sunflower oil) by the company Provital, which contains carotenoids, vitamin E and vitamin K ; tyrosine and / or its derivatives, known for their effect on the acceleration of the tanning of human skin in association with exposure to ultraviolet radiation, such as for example the product marketed under the brand name "SunTan Accelerator ™" by the company Provital which contains tyrosine and riboflavins (vitamin B), the tyrosine and tyrosinase complex marketed under the brand name "Zymo Tan Complex" by the company Zymo Line, the product marketed under the brand name MelanoBronze ™ (INCI name: Acetyl Tyrosine, Monk's pepper extract (Vitex Agnus-castus)) by the company Mibelle which contains acetyl tyrosine, product marketed under the brand name Unipertan VEG-24/242/2002 (INCI name: butylene glycol and Acetyl Tyrosine and hydrolyzed vegetable protein and Adenosine triphosphate) by the company UNIPEX, the product marketed under the brand name "Try-Excell ™" (INCI name: Oleoyl Tyrosine and Luffa Cylin drica (Seed) Oil and Oleic acid) by the company Sederma which contains extracts of pumpkin seeds (or Loofah oil), the product marketed under the brand name "Actibronze ™" (INCI name: hydrolyzed wheat protein and acetyl tyrosine and copper gluconate) by the company Alban Muller, the product marketed under the brand name Tyrostan ™ (INCI name: potassium caproyl tyrosine) by the company Synerga, the product marketed under the brand name Tyrosinol (INCI name: Sorbitan Isostearate, glyceryl oleate, caproyl Tyrosine) by the company Synerga, the product marketed under the brand name InstaBronze ™ (name INCI: Dihydroxyacetone and acetyl tyrosine and copper gluconate) marketed by the company Alban Muller, the product marketed under the brand name Tyrosilane ( INCI: methylsilanol and acetyl tyrosine) by the company Exymol; peptides known for their activation effect of melanogenesis such as for example the product marketed under the brand name Bronzing SF Peptide powder (INCI name: Dextran and Octapeptide-5) by the company Infinitec Activos, the product marketed under the name Melitane brand (INCI name: Glycerin and Aqua and Dextran and Acetyl hexapeptide1) including acetyl hexapeptide-1 known for its agonist action of alpha-MSH, the product marketed under the brand name Melatimes Solutions ™ (INCI name: Butylene glycol, Palmitoyl Tripeptide-40) by the company LIPOTEC, sugars and sugar derivatives such as for example the product marketed under the brand name Tanositol ™ (INCI name: inositol) by the company Provital, the product marketed under the name brand Thalitan ™ (or Phycosaccharide ™ AG) by the company CODIF international (INCI name: Aqua and hydrolyzed algin (Laminaria Digitata) and magnesium sulfate and manganese sulfate) contains ant an oligosaccharide of marine origin (guluronic acid and mannuronic acid chelated with magnesium and manganese ions), the product marketed under the brand name Melactiva ™ (INCI name: Maltodextrin, Mucuna Pruriens Seed extract) by the company Alban Muller, compounds rich in flavonoids such as for example the product marketed under the brand name "Biotanning" (INCI name: Hydrolyzed citrus Aurantium dulcis fruit extract) by the company Silab and known to be rich in lemon flavonoids (hesperidin type);
    - Mineral fillers or pigments, such as titanium dioxide, brown iron oxides, yellow iron oxides, black iron oxides, or red iron oxides or even white or colored pearlescent pigments such as Mica-Titanium.
    - Particles providing a visual effect or intended for the encapsulation of active ingredients,
    - Exfoliating particles,
    - Optical brighteners,
    - Insect repellants.
    The oil-in-water emulsion (E) as defined above can be packaged in a bottle, in a device of the pump bottle type, in pressurized form in an aerosol device, in a device provided with a perforated wall like a grid. or in a device fitted with a ball applicator (called roll-on).
    The invention also relates to the use of an emulsion of the oil-in-water type for topical use (E) as defined above for the protection of human skin against the unsightly effects of exposure to ultra- purple of the sun, and more particularly against redness.
    The subject of the invention is finally an emulsion an emulsion of oil-in-water type (E) comprising for 100% of its mass:
    - From 50% to 90% by mass, more particularly from 60% to 90% by mass and even more particularly from 70% to 90% by mass of a cosmetically acceptable aqueous phase (A),
    - From 10% to 50% by mass, more particularly from 10% to 40% by mass and even more particularly from 10% to 30% by mass of an fatty phase (G) comprising for 100% of its mass:
    - From 10% to 50% by mass, more particularly from 15% to 40% by mass of a mixture (MJ of cyclic or acyclic, linear or branched saturated hydrocarbons among which at least 95% by mass comprises from fifteen to nineteen atoms of carbon;
    - From 0.5% to 15% by mass, more particularly from 1% to 10% by mass of at least one surfactant of the oil-in-water type,
    - From 5% to 30% by mass, more particularly from 15% to 30% by mass of at least one agent for protection against ultraviolet radiation from the sun,
    - From 0% to 80% by mass, more particularly from 0% to 60% by mass of at least one oil and / or a wax, it being understood that such an oil and / or such a wax does not meet the definition of said mixture (Mi), for use in a method of therapeutic treatment intended to prevent and / or treat diseases of the human skin linked to exposure to ultraviolet radiation from the sun, more particularly burns, sunburns, erythema, skin cancer.
    The following examples illustrate the invention without, however, limiting it.
    Preparation of oil-in-water emulsions according to the invention, comprising a mixture (Mfl, and of comparative oil-in-water emulsions.
    Four oil-in-water emulsions according to the invention are prepared, denoted (E ^ to (E 4 ), the mass proportions of their constituents of which are given in Table 1, and six comparative oil-in-water emulsions denoted (Ffl to (F 5 ) whose mass proportions of their constituents are indicated in Table 2 below. The common preparation process for the oil-in-water emulsions according to the invention and for the comparative oil-in-water emulsions, is the following:
    - The oily mixture to be tested is poured into a beaker, at a temperature of 20 ° C., then optionally a possible second oil is gradually dispersed with mechanical stirring at 80 rpm;
    - The required amount of the thickening agent SEPINOV ™ EMT 10 is then added thereto with mechanical stirring at 80 revolutions / minute and at 20 ° C;
    - The aqueous phase comprising water and Oramix ™ NS10 is prepared by mixing in a beaker, at a temperature of 20 ° C.,
    - The mixture then obtained is cooled with stirring of the deflocculating type at 1500 revolutions per minute for twenty minutes, then drained to obtain the desired oil-in-water emulsion.
    Emulsion (Ei) (E 2 ) (Es) (E 4 ) Fat phase Sepinov ™ EMT10 (1) 2% 2% 2% 2% Emosmart ™ L19 (2 15% 0% 12% 3% Emogreen ™ L15 (3) 0% 15% 3% 12% Aqueous phase Water Qs. 100% Qs. 100% Qs. 100% Qs. 100% Oramix ™ NS 10 (4) 0.3% 0.3% 0.3% 0.3%
    Table 1 (1) (Sepinov ™ EMT10): Thickening agent (INCI name: hydroxyethyl acrylate / acryloyldimethyltaurate acrylate copolymer), (2) (Emosmart ™ L19): Mixture of saturated cyclic or acyclic, linear or branched hydrocarbons comprising for 100% of its mass:
    i) 13.20% by mass of linear alkanes having from 15 to 19 carbon atoms, ii) 55.00% by mass of iso-alkanes having from 15 to 19 carbon atoms, iii) 31.80% of cyclo alkanes having from 15 to 19 carbon atoms;
    (3) (Emogreen ™ L15): Mixture comprising for 100% of its mass:
    i) 3.7% of linear alkanes containing from 15 to 19 carbon atoms, ii) 96% of iso-alkanes comprising from 15 to 19 carbon atoms, iii) 0.3% of cyclo-alkanes comprising 15 to 19 carbon atoms;
    (4) (Oramix ™ NS10): solubilizing foaming agent (INCI name capryloyl / capryl glucoside).
    Emulsion (Fi) (F 2 ) (F 3 ) (F 4 ) (F 5 ) Fat phase Sepinov ™ EMT10 2% 2% 2% 2% 2% Isohexadecane 15% 0% 0% 0% 0% DC 345 (S) 0% 15% 0% 0% 0% DC 245 (6) 0% 0% 15% 0% 0% Emosmart ™ L15 (7) 0% 0% 0% 15% 0% Emosmart ™ V21 (8) 0% 0% 0% 0% 15% Aqueous phase Water Qs. 100% Qs. 100% Qs. 100% Qs. 100% Qs. 100% Oramix ™ NS10 0.3% 0.3% 0.3% 0.3% 0.3%
    Table 2 (5) (DC 345): Emollient agent used in cosmetics for the sensory properties which it provides and more particularly the ease of spreading which it confers on the emulsion containing it (INCI name cyclopentasiloxane &cyclohexasiloxane);
    (6) (DC 245): Emollient agent used in cosmetics for the sensory properties which it provides and more particularly the ease of spreading which it confers on the emulsion containing it; (INCI name INCI name cyclopentasiloxane) (7) (Emosmart ™ L15): Mixture comprising for 100% of its mass:
    i) 9.26% by mass of linear alkanes having from 13 to 15 carbon atoms, ii) 39.06% by mass of iso-alkanes having from 13 to 15 carbon atoms, iii) 51.68% of cyclo alkanes having from 13 to 15 carbon atoms;
    (8) (Emosmart ™ V21): Mixture comprising for 100% of its mass:
    i) 15.99% by mass of linear alkanes containing from 18 to 21 carbon atoms, ii) 59.90% by mass of iso-alkanes comprising from 18 to 21 carbon atoms, iii) 24.11% of cyclo alkanes having from 18 to 21 carbon atoms.
    Evaluation of the spreading properties of an oil-in-water emulsion according to the invention and of comparative oil-in-water emulsions
    Principle of the method
    The spreading properties of an oil-in-water emulsion are evaluated by the variation of an average of measurements of the value of the coefficient of friction of said emulsion, carried out using a rheometer of the DHR2 type (of Texas Instrument), for different spreading speeds.
    Principle of measurement
    It is a question of characterizing each emulsion tested by an average value of 3 measured values of the coefficient of friction, in normal force, for a velocity of 1 radian.s ' 1 and 4 radian.s' 1 , then to calculate the percentage evolution for the average obtained at each of the two speeds.
    Material and apparatus
    The measurements are carried out using a DHR2 rheometer (TA Instrument) equipped with the "Tribo Ring on Plate" type accessory on which a plexiglass surface is placed on which the emulsion to be tested is deposited.
    Procedure
    - We deposit, using a calibrated spreader, a quantity of the emulsion to be tested such that it forms a thickness of 90 micrometers on the plan.
    - After depositing the sample, put its calibrated thickness in contact with the “Tribo Ring on Plate” geometry, and apply a normal force of 2 N and a fixed velocity gradient that can be set to a value between 0, 01 and 15 radian.s' 1 .
    - We measure the maximum normal friction force undergone by the Peltier plane during the rotation of the geometry.
    Expression of results
    For each emulsion tested, and for each measurement carried out of the value of the maximum normal friction force, the friction coefficient (Cf) is calculated as follows:
    Cf = (maximum normal force friction value) / (normal force applied value)
    For each emulsion tested, we consider the values obtained during 3 statistically significant measurements, for a velocity set at 1 radian.s ' 1 and for a velocity set at 4 radian.s' 1 , and for each of the emulsions tested, we calculate the average value of the values of the coefficients of friction thus experimentally obtained noted Cfm1 for a velocity fixed at 1 radian.s ' 1 and Cfm4 for a velocity fixed at 4 radian.s' 1 .
    We then calculate the variation (denoted ACf) between the average value of the coefficient of friction obtained for a velocity of 1 radian.s' 1 and the average value of the coefficient of friction obtained for a velocity of for a velocity set at 4 radian.s ' 1 as follows:
    Acf - (Cf m i - Cf m 4) / (Cf m i) x 100
    Results
    The results obtained are reported in Table 3 below.
    Emulsion (Ei) (Fi) (F 2 ) (F 3 ) -6.8% + 18.2% + 17.5% + 14.5%
    Table 3
    Results analysis
    The results recorded in table 3 clearly show that the variation of the means of the friction coefficients, between a spread at a velocity of 1 radian.s ' 1 and a velocity of 4 radian.s' 1 for the emulsion (Ei) according to the invention is less than a value of 10% (-6.8%) while the comparative emulsions (F 2 ) and (F 3 ), comprising silicone oils known to impart an improvement in spreading to the emulsions who understand it, show a variation in the coefficient of friction greater than 15% between spreading at a velocity of 1 radian.s ' 1 and a velocity of 4 radian.s' 1 .
    These results thus show an improvement in the ease of spreading the emulsions according to the invention compared with emulsions comprising emollient agents known to provide ease of spreading in emulsions comprising it.
    The variation in the means of the friction coefficients, between spreading at a velocity of 1 radian.s ' 1 and a velocity of 4 radian.s' 1 for the comparative emulsion (FJ, comprising isohexadecane, ie an iso-paraffin comprising 16 carbon atoms, shows a value of 18.2%, that is to say a lower performance and a lesser ease of spreading for the emulsions comprising this iso-paraffin comprising 16 carbon atoms than for the emulsions according to the invention.
    Finally, the negative variation in the mean of the coefficients of friction, between a velocity of 1 radian.s ' 1 and a velocity of 4 radian.s' 1 , shows an additional technical benefit, namely obtaining a lower average value of the coefficient of friction for a low velocity, ie a possibility of spreading the emulsion according to the invention more easily on the skin.
    Evaluation of the sensory properties of oil-in-water emulsions according to the invention and of comparative oil-in-water emulsions
    Principle of the method
    Thirteen duly trained and qualified panelists evaluated the criteria of sensation of richness of shine of the skin and shine of the emulsion of oil-in-water emulsions according to the invention and of comparative oil-in-water emulsions, taking as reference base an emulsion known by the person skilled in the art as constituting an emulsion for which the richness criterion is recognized by all of the panelists, as well as a comparison reference to be surpassed in order to realize the technical problem posed.
    Procedure
    The operating mode implemented comprises 5 steps which are as follows:
    - Step 1 control and evaluation of the appearance and odor of the oil-in-water emulsion tested,
    - Step 2: handling: evaluation of the ease of grasping, and observation of a possible shooting aspect,
    - Step 3: spreading the emulsion tested on the skin by circular application to the surface of the skin, at the same speed for 10 turns, and collection of the sensations perceived at the end of the 10 th turn,
    - Step 4: further spreading of the tested emulsion on the skin always by applying the same circular movement until the absence of emulsion film is observed on the skin and collection of the perceived sensations,
    - Step 5: collection of the sensations perceived after 1 minute after the end of the spreading.
    This procedure is carried out at a temperature of 20 ° C.
    Expression of results
    For each emulsion tested, and for each sensory criterion evaluated, each panelist indicates whether said tested emulsion provides an improved sensation compared to the reference emulsion. All of the evaluations are collected and the data are processed statistically so as to determine the significance of any difference, improvement or deterioration, between the sensation perceived for the emulsion tested and the reference emulsion.
    Results
    Feeling of wealth criterion
    - Reference emulsion: emulsion (F 4 ).
    The emulsions according to the invention (E ^ and (E 3 ), as well as the comparative emulsions (F 2 ) and (F 5 ) are evaluated according to the protocol defined above and the results obtained are recorded in Table 4 below. The improvement in the feeling of richness compared to (F 4 ) is noted> (F 4 ) and the deterioration in the feeling of richness compared to (F 4 ) is noted <(F 4 ) at each moment of the spreading process.
    Emulsion (Ei) (Es) (F 2 ) (F 5 ) Step 1: Visual assessment > (F 4 ) > (F 4 ) <(F 4 ) <(F 4 ) Step 2: Gripping assessment > (F 4 ) > (F 4 ) <(F 4 ) <(F 4 ) Step 3: Evaluation after the first 10 rounds > (F 4 ) > (F 4 ) <(F 4 ) <(F 4 ) Step 4: Evaluation after penetration > (F 4 ) > (F 4 ) <(F 4 ) <(F 4 ) Step 5: Evaluation 1 minute after end of spreading > (F 4 ) > (F 4 ) <(F 4 ) <(F 4 )
    Table 4
    Skin gloss criterion
    - Reference emulsion: emulsion (F 4 );
    The emulsions according to the invention (E ^ and (E 3 ), as well as the comparative emulsions (F 2 ) and (F 5 ) are evaluated according to the protocol defined above and the results obtained are recorded in Table 5 below. The increase in the brightness of the skin compared to (F 4 ) is noted> (F 4 ) and its decrease noted <(F 4 ).
    Emulsion (Ei) (Es) (Fs) (F 5 ) Step 5: Evaluation 1 minute after end of spreading <(F 4 ) <(F 4 ) > (F 4 ) > (F 4 )
    Table 5
    Emulsion gloss criterion
    The emulsions according to the invention (E ^ and (E 3 ), as well as the comparative emulsions (F 2 ) and (F 5 ) are evaluated according to the protocol defined above and the results obtained are recorded in Table 5 below. The increase in the gloss of the emulsion compared to (F 4 ) is noted> (F 4 ) and its decrease noted <(F 4 ).
    Emulsion (Ei) (Es) (F 2 ) (F 6 ) Step 1: Visual assessment > (F 4 ) > (F 4 ) <(F 4 ) <(F 4 )
    Table 6
    Results analysis
    The results obtained show the improvement of the sensory and aesthetic properties thanks to the process according to the invention.
    Illustrative formulas
    Solar emulsion
    Ingredients % (mass) Polyacrylate Crosspolymer-6 (SEPIMAX ™ ZEN) 0.90% Glycerin 1.50% Aqua Qsp 100% Easynov ™ 3.00% EMOGREEN ™ L15 12.00% Sepicide ™ HB 1.00% Fragrance 0.30% Titanium Dioxide And Alumina And Stearic Acid 10.00%
    High UV protection solar fluid
    Ingredients % (mass) Montanov ™ 82 2.00% C12-15 Alkyl Benzoate 17.00% Octocrylene 6.00% Ethylhexyl Methoxycinnamate 6.00% Bis-Ethylhexylphenol Methoxyphenyl triazine 3.00% Emogreen ™ L19 3.00% Tocopherol 0.05% Polyacrylate Crosspolymer-6 (SEPIMAX ™ ZEN) 0.25% Cyclopentasiloxane 5.00% Titanium Dioxide And Isohexadecane And Triethylhexanoin AndAluminum Stearate And Alumina And Polyhydroxystearic Acid 5.40% Aqua Qsp 100% Methylene Bis-Benzotriazolyl Tetramethylbutylphenol 10.00% Citric Acid QspH 5.5
    Aquaxyl ™ 3.00% Phenoxyethanol Ethylhexylglycerin 1.00% Fragrance 0.20%
    High UV protection solar fluid
    Ingredients % (mass) Montanov ™ 82 2.00% C12-15 Alkyl Benzoate 17.00% Octocrylene 6.00% Ethylhexyl Methoxycinnamate 6.00% 2-ethylhexyl dimethoxybenzylidene dioxoimidazolidine propionate 3.00% Emogreen ™ L15 3.00% Tocopherol 0.05% Polyacrylate Crosspolymer-6 (SEPIMAX ™ ZEN) 0.25% Cyclopentasiloxane 5.00% Titanium Dioxide And Isohexadecane And Triethylhexanoin AndAluminum Stearate And Alumina And Polyhydroxystearic Acid 5.40% Aqua Qsp 100% Methylene Bis-Benzotriazolyl Tetramethylbutylphenol 10.00% Citric Acid QspH 5.5 Aquaxyl ™ 3.00% Phenoxyethanol Ethylhexylglycerin 1.00% Fragrance 0.20%
    Hair balm
    Ingredients % (mass) Aqua Qsp 100% Glycerin 1.50% Propanediol 1.50% Polyacrylate Crosspolymer-6 (SEPIMAX ™ ZEN) 1.50% Cera Alba 2.00% Copernica Cerifera 1.00% Butyrospermum parkii 2.00%
    Prunus amygdalus dulcis 4.00% Simmondsia chinensis seed oil 6.00% Emogreen ™ L15 3.00% Montanov ™ 202 2.50% Cetearyl Alcohol 3.00% Aquaxyl ™ 3.00% Tocopherol & Helianthus annuus seed oil 0.10% Benzyl alcohol & Dehydroacetic acid 0.70% Citrus aurantium peel oil 0.20% Sodium chloride 1.00% Sodium Hydroxide QspH 5.5
    SEPIMAX ™ Zen (Polyacrylate Crosspolymer-6) is a thickening and stabilizing anionic polymer, sold by the company SEPPIC
    EASYNOV ™ (Octyldodecanol & Octydodecyl Xyloside & PEG-30 Dipolyhydroxystearate) is a water-in-oil emulsifier, sold by the company SEPPIC
    SOLAGUM ™ AX (Acacia Senegal Gum and Xanthan Gum) is a thickening and stabilizing polymer of natural origin, sold by the company SEPPIC.
    Montanov ™ 82 (Cetearyl Alcohol & Cocoglucoside) is an emulsifying agent of the oil-in-water type, sold by the company SEPPIC
    AQUAXYL ™ (Xylitylglucoside and Anhydroxylitol and Xylitol) is a moisturizing active agent sold by the company SEPPIC.
    SEPICIDE ™ HB (Phenoxyethanol & Methylparaben & Ethylparaben & Propylparaben & Butylparaben) is a preservative composition marketed by the company SEPPIC. “Citrus Waterfall” perfume concentrate is marketed by the company Mane
    Montanov ™ 202 (Arachidyl Alcohol (and) Behenyl Alcohol. (And) Arachidyl Glucoside) is an emulsifier of oil-in-water type, sold by the company SEPPIC
    权利要求:
    Claims (12)
    [1" id="c-fr-0001]
    1. Method for improving the sensory and / or aesthetic properties of an emulsion for topical use (E o ) of the oil-in-water type, characterized in that an effective amount of a mixture (Mfi d 'saturated cyclic or acyclic, linear or branched hydrocarbons of which at least 95% by mass contain from fifteen to nineteen carbon atoms.
    [2" id="c-fr-0002]
    2. method as defined in claim 1, characterized in that said mixture (Mfi comprises for 100% of its mass:
    - A mass proportion of branched alkanes greater than or equal to 80% and less than or equal to 100%;
    - A mass proportion of linear alkanes greater than or equal to 0% and less than or equal to 15%;
    - A mass proportion of cycloalkanes greater than or equal to 0% and less than or equal to 5%, in that from 95% by mass to 100% by mass of said cyclic or acyclic hydrocarbons, linear or branched, comprise from fifteen to nineteen carbon atoms, and in that up to 5% by mass of said cyclic, acyclic, linear or branched hydrocarbons contain less than fifteen carbon atoms or more than nineteen carbon atoms.
    [3" id="c-fr-0003]
    3. Method as defined in claim 1, characterized in that said mixture (Mfi comprises for 100% of its mass:
    - A proportion by mass of branched alkanes greater than or equal to 40% and less than or equal to 100%, and more particularly greater than or equal to 50% by mass,
    - A mass proportion of linear alkanes greater than or equal to 0% and less than or equal to 20%, and more particularly less than or equal to 15% by mass
    - A mass proportion of cycloalkanes greater than or equal to 0% and less than or equal to 40% and more particularly less than or equal to 35% by mass, and in that 100% by mass of said cyclic or acyclic hydrocarbons, linear or branched, comprise from fifteen to nineteen carbon atoms.
    [4" id="c-fr-0004]
    4. Method as defined in any one of claims 1 to 3, characterized in that the sensory properties are the spreading properties of said emulsion for topical use (E o ).
    i
    [5" id="c-fr-0005]
    5. Method as defined in any one of claims 1 to 3, characterized in that the sensory properties are the properties of consistency and richness of said emulsion for topical use (E o ).
    [6" id="c-fr-0006]
    6. Method as defined in any one of claims 1 to 3, characterized in that the aesthetic property is the brightness of said emulsion for topical use (E o ).
    [7" id="c-fr-0007]
    7. Method as defined in any one of claims 1 to 3, characterized in that the aesthetic property is the matt appearance of the skin observed after the application to the skin of said emulsion for topical use (E o ).
    [8" id="c-fr-0008]
    8. Emulsion for topical use of oil-in-water type (E) comprising for 100% of its mass:
    - From 50% to 90% by mass, of a cosmetically acceptable aqueous phase (A),
    - From 10% to 50% by mass, of an oily phase (G) comprising for 100% of its mass:
    - From 10% to 50% by mass, more particularly from 15% to 40% by mass of a mixture (MJ of cyclic or acyclic, linear or branched saturated hydrocarbons among which at least 95% by mass comprises from fifteen to nineteen atoms of carbon;
    - From 0.5% to 15% by mass, of at least one oil-in-water type surfactant,
    - From 5% to 30% by mass, of at least one agent for protection against ultraviolet radiation from the sun,
    - From 0% to 80% by mass, of at least one oil and / or a wax, it being understood that such an oil and / or such a wax does not meet the definition of said mixture (MJ.
    [9" id="c-fr-0009]
    9. Oil-in-water emulsion for topical use (E) as defined in claim 8, characterized in that the agent for protection against ultraviolet radiation from the sun is chosen from the elements of the group consisting of titanium, 2,4-dihydroxy benzophenone, 2- (4-diethylamino-2-hydroxybenzoyl) benzoic acid hexyl ester, 2,4bis {[4- (2-ethylhexyloxy) -2-hydroxy] phenyl} -6- (4-methoxyphenyl) -1,3,5-triazine, 2,4,63060322 tris [4- (2-ethylhexyloxy carbonyl) anilino] -1,3,5-triazine and 2-ethylhexyl dimethoxy benzylidene dioxoimidazolidine propionate.
    [10" id="c-fr-0010]
    10. Oil-in-water emulsion (E) as defined in any one of claims 8 or 9, characterized in that said mixture (IVh) comprises for 100% of its mass:
    - A mass proportion of branched alkanes greater than or equal to 80% and less than or equal to 100%,
    - A mass proportion of linear alkanes greater than or equal to 0% and less than or equal to 15%,
    - A mass proportion of cycloalkanes greater than or equal to 0% and less than or equal to 5%, in that from 95% by mass to 100% by mass of said cyclic or acyclic hydrocarbons, linear or branched, comprise from fifteen to nineteen carbon atoms and in that up to 5% by mass of said cyclic, acyclic, linear or branched hydrocarbons contain less than fifteen carbon atoms or more than nineteen carbon atoms.
    [11" id="c-fr-0011]
    11. Oil-in-water emulsion (E) as defined in any one of claims 8 or 9, characterized in that said mixture (MO comprises for 100% of its mass:
    - A proportion by mass of branched alkanes greater than or equal to 40% and less than or equal to 100%, and more particularly greater than or equal to 50% by mass,
    - A mass proportion of linear alkanes greater than or equal to 0% and less than or equal to 20%, and more particularly less than or equal to 15% by mass
    - A mass proportion of cycloalkanes greater than or equal to 0% and less than or equal to 40% and more particularly less than or equal to 35% by mass, and in that 100% by mass of said cyclic or acyclic hydrocarbons, linear or branched, comprise from fifteen to nineteen carbon atoms.
    [12" id="c-fr-0012]
    12. Emulsion for topical use of oil-in-water type (E) comprising for 100% of its mass:
    - From 50% to 90% by mass, of a cosmetically acceptable aqueous phase (A),
    - From 10% to 50% by mass, of an oily phase (G) comprising for 100% of its mass:
    - From 10% to 50% by mass, more particularly from 15% to 40% by mass of a mixture (MJ of cyclic or acyclic saturated hydrocarbons, linear or branched from
    5 which at least 95% by mass contains from fifteen to nineteen carbon atoms;
    - From 0.5% to 15% by mass, of at least one oil-in-water type surfactant,
    - From 5% to 30% by mass, of at least one agent for protection against ultraviolet radiation from the sun,
    - From 0% to 80% by mass, of at least one oil and / or one wax, it being understood that such an oil and / or such a wax does not meet the definition of said mixture (MJ, for its use in a therapeutic treatment method intended to prevent and / or treat diseases of the human skin linked to exposure to ultraviolet radiation from the sun, more particularly burns, sunburns, erythemas, skin cancers.
    类似技术:
    公开号 | 公开日 | 专利标题
    EP2983792B1|2017-05-03|Novel oil-in-water emulsions with a high aqueous phase content, liquid consistencies and storage stability
    EP3554462A1|2019-10-23|Method for improving the sensorial properties of oil-in-water emulsions
    EP3285719B1|2019-08-28|Novel cosmetic emulsions provided in foam form, method for obtaining same and cosmetic use thereof
    WO2015078893A1|2015-06-04|Composition of alkyl polyglucosides and fatty esters of cationic amino acids
    EP3261727B1|2019-07-03|Obtaining an extract from brown algae gametophytes, and use of said extract as a cosmetic anti-aging active principle
    EP3280427A1|2018-02-14|Method for culturing cells of acrochaetium moniliforme red algae, method for obtaining an extract of the biomass thereof, and use of same in cosmetics
    EP3661478B1|2021-05-05|Novel surfactant composition, production method thereof, and use of same as an emulsifier for the production of topical oil-in-water emulsions
    FR3074686B1|2019-11-15|NEW GLYCERYL POLYRHAMNOSIDES, PROCESS FOR THEIR PREPARATION AND COSMETIC AND / OR PHARMACEUTICAL COMPOSITION COMPRISING THE SAME
    EP3723720B1|2022-01-05|New polyol polyrhamnosides, process for the preparation thereof, and cosmetic and/or pharmaceutical composition comprising same
    FR3094212A1|2020-10-02|Alkane and ester-based compositions which are stable on temperature storage, their use as emollients and emulsions comprising them
    FR3060321A1|2018-06-22|PROCESS FOR IMPROVING THE SENSORY PROPERTIES OF OIL-IN-WATER EMULSIONS TO REDUCE THE STICK EFFECT OF SAID OIL-IN-WATER EMULSIONS BASED ON GLYCERIN
    FR3034988A1|2016-10-21|NOVEL COSMETIC EMULSIONS PRESENTED IN THE FORM OF FOAM, PROCESS FOR OBTAINING THEM AND USE THEREOF IN COSMETICS
    FR3104161A1|2021-06-11|Inverse latex for cosmetic composition comprising a particular sequestering agent and a polyelectrolyte combining strong acid function and weak acid function
    WO2021116000A1|2021-06-17|Inverse latex for a cosmetic composition comprising a specific chelating agent and a polyelectrolyte combining a strong acid function and a neutral function
    FR3104157A1|2021-06-11|Inverse latex for cosmetic composition combining a particular sequestering agent and a polyelectrolyte comprising a weak acid function
    FR3099700A1|2021-02-12|Composition for anhydrous topical use in the form of a dispersed phase based on at least one short diol in a continuous fatty phase
    FR3074687A1|2019-06-14|NOVEL ALKYL POLYRHAMNOSIDES, PROCESS FOR THEIR PREPARATION AND COSMETIC AND / OR PHARMACEUTICAL COMPOSITION COMPRISING THE SAME
    FR3029410A1|2016-06-10|USE OF 1,3-BUTANEDIOL ESTERS AND N-ACYL DERIVATIVES OF AMINO ACIDS AS A BROWNING AND / OR TANNING AGENT OF HUMAN SKIN
    FR3027519A1|2016-04-29|USE OF ISOSORBID ESTERS AND N-ACYL DERIVATIVES OF AMINO ACIDS AS A BROWNING AND / OR TANNING AGENT FOR HUMAN SKIN
    同族专利:
    公开号 | 公开日
    EP3554462A1|2019-10-23|
    BR112019012282A2|2019-11-19|
    US20220071861A1|2022-03-10|
    KR20190113770A|2019-10-08|
    FR3060322B1|2020-01-03|
    CN110461299A|2019-11-15|
    AU2017374588A1|2019-07-11|
    US20200093713A1|2020-03-26|
    WO2018109354A1|2018-06-21|
    JP2020505320A|2020-02-20|
    引用文献:
    公开号 | 申请日 | 公开日 | 申请人 | 专利标题
    WO2008155060A2|2007-06-19|2008-12-24|Cognis Ip Management Gmbh|Hydrocarbon mixtures and use thereof|
    FR2761595B1|1997-04-04|1999-09-17|Oreal|COMPOSITIONS COMPRISING SANTALINES, SANTARUBINS FOR ARTIFICIAL COLORING OF THE SKIN AND USES THEREOF|
    AT371434T|2003-03-27|2007-09-15|Dow Corning|COMPOSITIONS WITH DELAYED RELEASE|
    WO2006094642A1|2005-03-04|2006-09-14|Cognis Ip Management Gmbh|Emollients and cosmetic compositions based on special branched hydrocarbons|
    JP5622359B2|2006-02-10|2014-11-12|デユポン・テイト・アンド・ライル・バイオ・プロダクツ・カンパニー・エルエルシー|Bio-derived 1,3-propanediol and its conjugated esters as natural non-irritating solvents for biomass-derived extracts, fragrance concentrates, and oils|
    US8679556B2|2006-09-22|2014-03-25|Societe Industrielle Limousine D'application Biologique |Process for obtaining an active ingredient with an immediate tensor effect on the skin, active ingredient and compositions|
    KR101655346B1|2009-11-27|2016-09-08|아모레퍼시픽|Cosmetic composition stabilized higher oily part|
    JP6071123B2|2012-02-10|2017-02-01|株式会社 資生堂|Oil-in-water emulsified skin cosmetic|CN113164784A|2018-12-19|2021-07-23|Lvmh研究公司|Oil-in-water type emulsion cosmetic with ultraviolet protection effect|
    FR3094212B1|2019-03-28|2021-04-09|Soc Dexploitation De Produits Pour Les Industries Chimiques Seppic|Alkane and ester-based compositions stable on temperature storage, their use as emollients and emulsions comprising them|
    EP3795134A1|2019-09-19|2021-03-24|Société d'Exploitation de Produits pour les Industries Chimiques SEPPIC|Perfuming compositions, stable and having good spraying properties|
    法律状态:
    2017-12-21| PLFP| Fee payment|Year of fee payment: 2 |
    2018-06-22| PLSC| Publication of the preliminary search report|Effective date: 20180622 |
    2018-12-20| PLFP| Fee payment|Year of fee payment: 3 |
    2019-12-19| PLFP| Fee payment|Year of fee payment: 4 |
    2020-12-23| PLFP| Fee payment|Year of fee payment: 5 |
    2021-12-24| PLFP| Fee payment|Year of fee payment: 6 |
    优先权:
    申请号 | 申请日 | 专利标题
    FR1662650|2016-12-16|
    FR1662650A|FR3060322B1|2016-12-16|2016-12-16|PROCESS FOR IMPROVING SENSORY PROPERTIES OF OIL-IN-WATER EMULSIONS|FR1662650A| FR3060322B1|2016-12-16|2016-12-16|PROCESS FOR IMPROVING SENSORY PROPERTIES OF OIL-IN-WATER EMULSIONS|
    EP17822400.2A| EP3554462A1|2016-12-16|2017-12-12|Method for improving the sensorial properties of oil-in-water emulsions|
    JP2019531316A| JP2020505320A|2016-12-16|2017-12-12|Method for improving sensory characteristics of oil-in-water emulsion|
    KR1020197019274A| KR20190113770A|2016-12-16|2017-12-12|Method for improving the sensory properties of oil-in-water emulsion|
    CN201780084471.7A| CN110461299A|2016-12-16|2017-12-12|Improve the method for the organoleptic attribute of oil-in-water emulsion|
    AU2017374588A| AU2017374588A1|2016-12-16|2017-12-12|Method for improving the sensorial properties of oil-in-water emulsions|
    US16/470,395| US20200093713A1|2016-12-16|2017-12-12|Method for improving the sensorial properties of oil-in-water emulsions|
    PCT/FR2017/053508| WO2018109354A1|2016-12-16|2017-12-12|Method for improving the sensorial properties of oil-in-water emulsions|
    BR112019012282-6A| BR112019012282A2|2016-12-16|2017-12-12|method for enhancing sensory properties of oil-in-water emulsions|
    US17/455,757| US20220071861A1|2016-12-16|2021-11-19|Method for improving the sensorial properties of oil-in-water emulsions|
    [返回顶部]