WO2003045337A2 - Cosmetic raw material, cosmetic product, and method for manufacturing a cosmetic product - Google Patents

Cosmetic raw material, cosmetic product, and method for manufacturing a cosmetic product Download PDF

Info

Publication number
WO2003045337A2
WO2003045337A2 PCT/JP2002/012400 JP0212400W WO03045337A2 WO 2003045337 A2 WO2003045337 A2 WO 2003045337A2 JP 0212400 W JP0212400 W JP 0212400W WO 03045337 A2 WO03045337 A2 WO 03045337A2
Authority
WO
WIPO (PCT)
Prior art keywords
group
groups
cosmetic
raw material
carbon atoms
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Ceased
Application number
PCT/JP2002/012400
Other languages
French (fr)
Other versions
WO2003045337A3 (en
Inventor
Haruhiko Furukawa
Yoshitsugu Morita
Takayuki Aso
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
DuPont Toray Specialty Materials KK
Original Assignee
Dow Corning Toray Silicone Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Dow Corning Toray Silicone Co Ltd filed Critical Dow Corning Toray Silicone Co Ltd
Priority to US10/496,022 priority Critical patent/US7488492B2/en
Priority to EP02791950A priority patent/EP1448154B1/en
Priority to AU2002361070A priority patent/AU2002361070A1/en
Priority to DE60222579T priority patent/DE60222579T2/en
Publication of WO2003045337A2 publication Critical patent/WO2003045337A2/en
Publication of WO2003045337A3 publication Critical patent/WO2003045337A3/en
Anticipated expiration legal-status Critical
Ceased legal-status Critical Current

Links

Classifications

    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q19/00—Preparations for care of the skin
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00—Cosmetics or similar toiletry preparations
    • A61K8/02—Cosmetics or similar toiletry preparations characterised by special physical form
    • A61K8/04—Dispersions; Emulsions
    • A61K8/046—Aerosols; Foams
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00—Cosmetics or similar toiletry preparations
    • A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/33—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
    • A61K8/37—Esters of carboxylic acids
    • A61K8/375—Esters of carboxylic acids the alcohol moiety containing more than one hydroxy group
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00—Cosmetics or similar toiletry preparations
    • A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
    • A61K8/91—Graft copolymers
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K2800/00—Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
    • A61K2800/40—Chemical, physico-chemical or functional or structural properties of particular ingredients
    • A61K2800/54—Polymers characterized by specific structures/properties
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q1/00—Make-up preparations; Body powders; Preparations for removing make-up
    • A61Q1/02—Preparations containing skin colorants, e.g. pigments
    • A61Q1/04—Preparations containing skin colorants, e.g. pigments for lips
    • A61Q1/06—Lipsticks
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q1/00—Make-up preparations; Body powders; Preparations for removing make-up
    • A61Q1/02—Preparations containing skin colorants, e.g. pigments
    • A61Q1/10—Preparations containing skin colorants, e.g. pigments for eyes, e.g. eyeliner, mascara
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q3/00—Manicure or pedicure preparations
    • A61Q3/02—Nail coatings
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q5/00—Preparations for care of the hair
    • A61Q5/02—Preparations for cleaning the hair
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q5/00—Preparations for care of the hair
    • A61Q5/06—Preparations for styling the hair, e.g. by temporary shaping or colouring
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q5/00—Preparations for care of the hair
    • A61Q5/12—Preparations containing hair conditioners

Definitions

  • the present invention relates to a cosmetic raw material, a cosmetic product, and a method for manufacturing a cosmetic product. Specifically, it relates to a cosmetic raw material exhibiting superior compounding stability in cosmetic products and capable of imparting excellent feel on application and surface protective properties to cosmetic products, to a cosmetic product obtained by compounding with the cosmetic raw material, and to a method for manufacturing the cosmetic product.
  • Cosmetic where used herein includes the application to the body for purposes other than beautifying, such as administering of materials to skin.
  • vinyl co-polymers of radical polymerizable monomers and organopolysiloxanes containing radical polymerizable groups have been known to be used as cosmetic raw materials.
  • Japanese Patent Application Publication No. Hei 5-000924 offers a base oil for a hair dressing agent consisting of a vinyl polymer obtained by polymerizing methacrylic acid and tertiary butyl acrylate with a dimethylpolysiloxane oligomer containing methacrylic groups. While this vinyl co-polymer does give water repellent properties and slip to cosmetic products, its compatibility with other cosmetic raw materials is low, and its compounding stability is inferior.
  • the inventors arrived at the present invention as a result of in-depth investigations aimed at overcoming the above-described problems. Namely, it is an object of the present invention to provide a cosmetic raw material exhibiting superior compounding stability in cosmetic products and capable of imparting excellent feel on application and surface protective properties to cosmetic products, a cosmetic product exhibiting superior adhesion to the hair and skin obtained by compounding with said cosmetic raw material, and a method for manufacturing the cosmetic product.
  • the present invention relates to a cosmetic raw material using a vinyl polymer containing carbosiloxane dendritic structures and fluorinated organic groups as its main or most important ingredient, a cosmetic product obtained by compounding with the cosmetic raw material, preferably by combining it with other raw materials or other cosmetic ingredients and a method for manufacturing the cosmetic product, in which the cosmetic raw material is mixed with other cosmetic ingredients or other raw materials.
  • the vinyl polymer used in the cosmetic raw material of the present invention is characterized by containing carbosiloxane dendritic structures and fluorinated organic groups. Structures, in which vinylic polymerized units constitute the backbone and carbosiloxane dendritic structures along with fluorinated organic groups are attached in side chains, are particularly preferable.
  • the carbosiloxane dendritic structures are high molecular structures obtained by regular high-degree branching from a single silicon atom. Structures represented by the formula(I):
  • Z is a divalent organic group exemplified by alkylene, arylene, aralkylene, ester-containing divalent organic groups, ether-containing divalent organic groups, ketone-containing divalent organic groups, and amide-containing divalent organic groups.
  • organic groups represented by the following formulas are preferable.
  • R 9 is an alkylene group with 1 to 10 carbon atoms exemplified by methylene, ethylene, propylene, and butylene.
  • R 10 is an alkyl group with 1 to 10 carbon atoms exemplified by methyl, ethyl, propyl, and butyl.
  • methyl is preferable.
  • R 1 ' is an alkylene group with 1 to 10 carbon atoms exemplified by methylene, ethylene, propylene, and butylene.
  • ethylene is preferable.
  • the subscript «d» is an integer of 0 to 4, and «e» is 0 or 1.
  • R 1 is an aryl or alkyl group with 1 to 10 carbon atoms, with alkyl groups exemplified by methyl, ethyl, propyl, butyl, pentyl, isopropyl, isobutyl, cyclopentyl, and cyclohexyl groups, and aryl groups exemplified by phenyl and naphthyl groups. Among the above, methyl and phenyl are preferable, and methyl is particularly preferable.
  • X 1 is a silylalkyl group represented by the following formula( ⁇ ) :
  • R 1 is the same as above.
  • R 2 is an alkylene group with 2 to 10 carbon atoms exemplified by ethylene, propylene, butylene, hexylene, and other linear alkylene groups; methylmethylene, methylethylene, 1-methylpentylene, 1,4-dimethylbutylene, and other branched alkylene groups.
  • ethylene, methylethylene, hexylene, 1- methylpentylene, and 1,4-dimethylbutylene are preferable.
  • R 3 is an alkyl group with 1 to 10 carbon atoms exemplified by methyl, ethyl, propyl, butyl, and isopropyl.
  • X l+1 is a group selected from the group comprising hydrogen atoms, aryl groups and alkyl groups with 1 to 10 carbon atoms, and the above-mentioned silylalkyl groups X 1 , with the alkyl and aryl groups exemplified by the same groups as the above-described R 1 .
  • the superscript «i» is an integer of 1 to 10 indicating the generation of the silylalkyl group, starting in each carbosiloxane dendritic structure with a value of 1 for the X 1 group in the formula(I), and «a'» is an integer of 0 to 3.
  • Groups represented by the formula: -(CH 2 ) x -(CF 2 ) y -R 13 are suggested as examples of fluoroalkyl groups obtained by substituting fluorine atoms for the hydrogen atoms of alkyl groups.
  • the subscript «x» is 0, 1, 2, or 3 and «y» is an integer of 1 to 20.
  • R 13 is an atom or group selected from a hydrogen atom, a fluorine atom, -CH(CF 3 ) 2 - or -CF(CF 3 ) 2 .
  • Such fluorine-substituted alkyl groups are exemplified by linear or branched polyfluoroalkyl or perfluoroalkyl groups represented by the formulas shown below.
  • fluoroalkyloxyfluoroalkylene groups obtained by substituting fluorine atoms for the hydrogen atoms of alkyloxyalkylene groups.
  • the subscript «m» is 0 or 1
  • «n» is 0, 1, 2, 3, 4, or 5
  • R 14 is a fluorine atom or CF 3 .
  • fluoroalkyloxyfluoroalkylene groups are exemplified by perfluoroalkyloxyfluoroalkylene groups represented by the formulas shown below.
  • Fluoroalkyl groups in general, and fluoroalkyl groups with 1 to 14 carbon atoms in particular, are preferable among such fluorinated organic groups from the standpoint of improving the oil repellency and skin-oil resistance of the cosmetic raw material of the present invention.
  • fluoroalkyl groups with 1 to 5 carbon atoms, and, more specifically, groups such as -CH 2 CF 3 are preferable when it is desirable to reduce stickiness.
  • the number average molecular weight of the vinyl polymer used in the present invention should preferably be between 3,000 and 2,000,000, and, even more preferably, between 5,000 and 800,000.
  • the polymer can be used in various forms, for example, in liquid, rubber, paste, solid, or powder form. When compounding in a cosmetic product, it is preferable to use it in powder form or in the form of a suspension or solution prepared by dissolving in a solvent.
  • This type of vinyl polymer is obtained by adding, if desired or necessary, (B) a vinyl monomer that does not have fluorinated organic groups in the molecule to (A) a vinyl monomer containing fluorinated organic groups in the molecule and (C) a carbosiloxane dendrimer containing radical polymerizable organic groups represented by the general formula(lTi): wherein Y is a radical polymerizable organic group and R 1 and X 1 are the same as above and subjecting them to co-polymerization.
  • R is a hydrogen atom or methyl group
  • R is a fluorinated organic group exemplified by the above-described fluoroalkyl and fluoroalkyloxyfluoroalkylene groups.
  • CH 2 CCH 3 COO-CF 3
  • CH 2 CCH 3 COO-C 2 F 5
  • CH 2 CCH 3 COO- nC 3 F 7
  • CH 2 CCH 3 COO-CF (CF 3 ) 2 .
  • CH 2 CCH 3 COO- nC 4 F 9
  • CH 2 CCH 3 COO-CF 2 CF(CF 3 ) 2 .
  • CH 2 CCH 3 COO- nCsFj i
  • CH 2 CCH 3 COO- nC 6 F 13 .
  • CH 2 CCH 3 COO- nC 8 F 17
  • CH 2 CCH 3 COO-CH 2 CF 3 .
  • CH 2 CCH 3 COO-CH(CF 3 ) 2 .
  • CH 2 CCH 3 COO-CH 2 CH(CF 3 ) 2
  • CH 2 CCH 3 COO-CH 2 (CF 2 ) 2 F.
  • CH 2 CCH 3 COO-CH 2 (CF 2 ) 3 F
  • CH 2 CCH 3 COO-CH 2 (CF 2 ) 4 F.
  • CH 2 CCH 3 COO-CH 2 (CF 2 ) 6 F
  • CH 2 CCH 3 COO-CH 2 (CF 2 ) 8 F.
  • CH 2 CCH 3 COO-CH 2 CH 2 CF 3
  • CH 2 CCH 3 COO-CH 2 CH 2 (CF 2 ) 2 F.
  • CH 2 CCH 3 COO-CH 2 CH 2 (CF 2 ) 3 F
  • CH 2 CCH 3 COO-CH 2 CH 2 (CF 2 ) 4 F.
  • CH 2 CCH 3 COO-CH 2 CH 2 (CF 2 ) 6 F
  • CH 2 CCH 3 COO-CH 2 CH 2 (CF 2 ) 8 F.
  • CH 2 CCH 3 COO-CH 2 CH 2 (CF 2 ) 10 F
  • CH 2 CCH 3 COO-CH 2 CH 2 (CF 2 ) 12 F.
  • CH 2 CCH 3 COO-CH 2 CH 2 (CF 2 ) 14 F
  • CH 2 CCH 3 COO-CH 2 CH 2 (CF 2 ) 16 F.
  • CH 2 CCH 3 COO-CH 2 CH 2 CH 2 (CF 2 ) 2 H
  • CH 2 CCH 3 COO-CH 2 (CF 2 ) 4 H.
  • CH 2 CCH 3 COO-CH 2 CH 2 CF(CF 3 )- [OCF 2 CF(CF 3 )] 2 -OC 3 F 7 .
  • CH 2 CCH 3 COO-CH 2 CH 2 CF 2 CF 2 - [OCF 2 CF(CF 3 )] z -OC 3 F 7 .
  • CH 2 CHCOO-CF 3 .
  • CH 2 CHCOO-C 2 F 5 .
  • CH 2 CHCOO-nC 3 F 7 .
  • CH 2 CHCOO-CF(CF 3 ) 2 .
  • CH 2 CHCOO-nC 4 F 9.
  • CH 2 CHCOO- CF 2 CF(CF 3 ) 2 .
  • CH 2 CHCOO-nC 5 F ⁇ .
  • CH 2 CHCOO- nC 6 F 13.
  • CH 2 CHCOO- nC 8 F 17.
  • CH 2 CHCOO-CH 2 CF 3 .
  • CH 2 CHCOO-CH(CF 3 ) 2.
  • CH 2 CHCOO-CH 2 CH(CF 3 ) 2 .
  • CH 2 CHCOO-CH 2 (CF 2 ) 2 F.
  • CH 2 CHCOO-CH 2 (CF 2 ) 3 F .
  • CH 2 CHCOO-CH 2 (CF 2 ) 4 F.
  • CH 2 CHCOO-CH 2 (CF 2 ) 6 F.
  • CH 2 CHCOO-CH 2 (CF 2 ) 8 F .
  • CH 2 CHCOO-CH 2 CH 2 CF 3 .
  • CH 2 CHCOO-CH 2 CH 2 (CF 2 ) 2 F.
  • CH 2 CHCOO-CH 2 CH 2 (CF 2 ) 3 F.
  • CH 2 CHCOO-CH 2 CH 2 (CF 2 ) 4 F.
  • CH 2 CHCOO-CH 2 CH 2 (CF 2 ) 6 F .
  • CH 2 CHCOO-CH 2 CH 2 (CF 2 ) 8 F.
  • CH 2 CHCOO-CH 2 CH 2 (CF 2 ) 10 F .
  • CH 2 CHCOO-CH 2 CH 2 (CF 2 ), 2 F.
  • CH 2 CHCOO-CH 2 CH 2 (CF 2 ) M F .
  • CH 2 CHCOO-CH 2 CH 2 (CF 2 ) ⁇ 6 F.
  • CH 2 CHCOO-CH 2 CH 2 CH 2 CF 3.
  • CH 2 CHCOO-CH 2 CH 2 CH 2 (CF 2 ) 2 F.
  • CH 2 CHCOO-CH 2 CH 2 CH 2 (CF) 2 H.
  • CH 2 CHCOO-CH 2 (CF 2 ) 4 H.
  • CH 2 CHCOO-CH 2 CH 2 (CF 2 ) 3 H.
  • CH 2 CHCOO-CH 2 CH 2 CF(CF 3 )-[OCF 2 CF(CF 3 )] z -OC 3 F 7 .
  • CH 2 CHCOO-CH 2 CH 2 CF 2 CF 2 -[OCF 2 CF(CF 3 )] z -OC 3 F 7 .
  • vinyl polymers represented by the formulas shown below are preferable.
  • CH 2 CHCOO-CH 2 CH 2 (CF 2 ) 6 F .
  • CH 2 CHCOO-CH 2 CH 2 (CF 2 ) 8 F.
  • CH 2 CCH 3 COO-CH 2 CH 2 (CF 2 ) 6 F .
  • CH 2 CCH 3 COO-CH 2 CH 2 (CF 2 ) 8 F.
  • CH 2 CHCOO-CH 2 CF 3 .
  • CH 2 CCH 3 COO-CH 2 CF 3
  • Vinyl polymers represented by the formulas shown below are particularly preferable.
  • CH 2 CHCOO-CH 2 CF 3 .
  • CH 2 CCH 3 COO-CH 2 CF 3.
  • the vinyl monomers (B) that do not contain fluorinated organic groups in the molecule may be any monomers having radical polymerizable vinyl groups, which are exemplified, for instance, by methyl acrylate, methyl methacrylate, ethyl acrylate, ethyl methacrylate, n- propyl acrylate, w-propyl methacrylate, isopropyl acrylate, isopropyl methacrylate, and other lower alkyl acrylates or methacrylates; glycidyl acrylate, glycidyl methacrylate; n- butyl acrylate, w-butyl methacrylate, isobutyl acrylate, isobutyl methacrylate, tert-butyl acrylate, tert-butyl methacrylate, «-hexyl acrylate, w-hexyl methacrylate, w-hexyl acrylate, w-
  • vinyl monomers (B) polyfunctional vinyl monomers, which are exemplified, for instance, by trimethylolpropane triacrylate, trimethylolpropane trimethacrylate, pentaerythritol triacrylate, pentaerythritol trimethacrylate, ethylene glycol diacrylate, ethylene glycol dimethacrylate, tetraethylene glycol diacrylate, tetraethylene glycol dimethacrylate, polyethylene glycol diacrylate, polyethylene glycol dimethacrylate, 1,4-butanediol diacrylate, 1,4-butanediol dimethacrylate, 1,6-hexanediol diacrylate, 1,6-hexanediol dimethacrylate, neopentyl glycol diacrylate, neopentyl glycol dimethacrylate, trimethylolpropane trioxyethyl acryl
  • the weight ratio of component (A) to component (B) should be within the range of from 0.1:99.9 to 100:0, and, preferably, within the range of from 1:99 to 100:0.
  • the carbosiloxane dendrimer (C) is represented by the general formula(i ⁇ ), indicated above.
  • Y is a radical polymerizable organic group, the type of which is not subject to any special limitations so long as this is an organic group capable of undergoing a radical addition reaction.
  • Acryl and methacryl-containing organic groups, alkenylaryl-containing organic groups, or alkenyl groups with 2 to 10 carbon atoms represented by the general formulas shown below are suggested as specific examples.
  • R 4 and R 6 are hydrogen atoms or methyl groups
  • R 5 and R are alkylene groups with 1 to 10 carbon atoms
  • R 7 is an alkyl group with 1 to 10 carbon atoms.
  • the subscript «b» is an integer of 0 to 4
  • «c» is 0 or 1.
  • Carbosiloxane dendrimers of this component with a generation number of 2 are represented by the general formula:
  • Carbosiloxane dendrimers of this component with a generation number of 3 are represented by the general formula:
  • Component (C) is exemplified by carbosiloxane dendrimers represented by the average composition formulas shown below.
  • CH 2 CH-Si ⁇ OSi-C 2 H 4 -Si-(OSi-CH 3 ) 3 ⁇ c
  • the carbosiloxane dendrimers of component (C) can be prepared using the preparation method for branched siloxane/silalkylene copolymers described in EP1055674. For example, they can be prepared by subjecting alkenyl-containing organic silicon compounds and silicon compounds containing silicon-bonded hydrogen atoms represented by the general formula:
  • the co-polymerization ratio of component (C), in terms of its weight ratio with respect to the total of component (A) and component (B), should be in the range of from 0.1 :99.9 to 99.9:0.1, preferably, in the range of from 1:99 to 99:1, and, even more preferably, in the range of from 5:95 to 95:5.
  • the vinyl polymers used in the present invention are prepared by co-polymerizing the above-described component (A), component (B), and component (C) or by polymerizing component (A) and component (C).
  • Radical polymerization and ion polymerization can be used as the polymerization methods, with radical polymerization being preferable and solution polymerization being especially suitable.
  • Solution polymerization is carried out by reacting the above-described components in a solvent in the presence of a radical initiator for 3 to 20 hours at a temperature of 50 to 150°C.
  • Solvents used at such time are exemplified by hexane, octane, decane, cyclohexane, and other aliphatic hydrocarbons; benzene, toluene, xylene, and other aromatic hydrocarbons; diethyl ether, dibutyl ether, tetrahydrofuran, dioxane, and other ethers; acetone, methyl ethyl ketone, methyl isobutyl ketone, diisobutyl ketone, and other ketones; methyl acetate, ethyl acetate, butyl acetate, isobutyl acetate, and other esters; methanol, ethanol, isopropyl alcohol, butanol, and other alcohols; octamethylcyclotetrasiloxane, decamethylcyclopentasiloxane, hexamethyldisiloxane, octa
  • the radical initiators are publicly known conventional compounds used for radical polymerization, specifically exemplified by 2,2'-azobis(isobutyronitrile), 2,2'-azobis(2- methylbutyronitrile), 2,2'-azobis(2,4-dimethylvaleronitrile), and other azobis compounds; benzoyl peroxide, lauroyl peroxide, tert-butyl peroxybenzoate, tert-butyl peroxy-2- ethylhexanoate, and other organic peroxides.
  • the radical initiators can be used singly or in combination as two or more initiators mixed together.
  • the amount of the radical initiator is preferably in the range of from 0.1 to 5 parts by weight per 100 parts by weight of the total of the above-described component (A) to component (C).
  • chain transfer agents can be added during polymerization.
  • Specific example of the chain transfer agents include 2-mercaptoethanol, butylmercaptan, «-dodecylmercaptan, 3- mercaptopropyltrimethoxysilane, mercaptopropyl-containing polydimethylsiloxanes, and other mercapto compounds; methylene chloride, chloroform, carbon tetrachloride, butyl bromide, 3-chloropropyltrimethoxysilane, and other halogen compounds.
  • amino groups can be introduced in the side chains of the vinyl polymer by using, as part of component (B), vinyl monomers containing amino groups, such as dimethyl aminoethyl acrylate, dimethyl aminoethyl methacrylate, diethyl aminoethyl acrylate, and diethyl aminoethyl methacrylate, and then performing modification with potassium monochloroacetate, ammonium monochloroacetate, aminomethylpropanol salt of monochloroacetic acid, triethanolamine salt of monobromoacetic acid, sodium monochloropropionate, and other alkali metal salts of halogenated fatty acids; otherwise, carboxylic acid groups can be introduced in the side chains of the vinyl polymer by using, as part of component (B), vinyl monomers containing carboxylic acids, such as acrylic acid, methacrylic acid, it
  • the cosmetic raw material of the present invention uses the above-described vinyl polymer containing carbosiloxane dendritic structures and fluorinated organic groups as its main or most important ingredient. Solutions or dispersions obtained by adding liquids selected from the group comprising silicone oil, organic oil, alcohol, and water to the vinyl polymer are suggested as examples of such materials.
  • the viscosity of such a solution or dispersion at 25°C is preferably in the range of from 10 to 1,000,000,000 mPa-s, and, even more preferably, in particular, from the standpoint of improving the feel of the cosmetic product, in the range of from 100 to 500,000,000 mPa-s.
  • the concentration of the vinyl polymer in the dispersion or solution is typically in the range of from 0.1 wt% to 95 wt%, and, preferably, in the range of from 1 wt% to 85 wt%. Furthermore, to make compounding and handling easier, it should preferably be in the range of from 5 wt% to 75 wt%.
  • silicone oils include, for instance, dimethylpolysiloxane having both ends of the molecular chain blocked by trimethylsiloxy groups, dimethylsiloxane/methylphenylsiloxane copolymer having both ends of the molecular chain blocked by trimethylsiloxy groups, dimethylsiloxane/methyl(3,3,3- trifluoropropyl)siloxane copolymer having both ends of the molecular chain blocked by trimethylsiloxy groups, and other linear non-reactive silicone oils, as well as cyclic compounds such as hexamethylcyclotrisiloxane, octamethylcyclotetrasiloxane, decamethylcyclopentasiloxane, and dodecamethylcyclohexasiloxane.
  • non-reactive silicone oils one may use modified polysiloxanes having polyether, amino, silanol, and other functional groups in the side chains or at
  • organic oils include, for instance, liquid paraffin, isoparaffin, hexyl laurate, isopropyl myristate, myristyl myristate, cetyl myristate, 2-octyldodecyl myristate, isopropyl palmitate, 2-ethylhexyl palmitate, butyl stearate, decyl oleate, 2-octyldodecyl oleate, myristyl lactate, cetyl lactate, lanolin acetate, stearyl alcohol, oleyl alcohol, avocado oil, almond oil, olive oil, cacao butter, jojoba oil, sesame oil, soybean oil, Camellia oil, squalane, persic oil, castor oil, mink oil, cottonseed oil, coconut oil, egg yolk oil, beef tallow, pork fat, polypropylene glycol monooleate, neopentyl glycol-2-
  • alcohols used in cosmetic raw materials may be utilized, methanol, ethanol, butanol, isopropyl alcohol, and other lower alcohols are preferable.
  • the vinyl polymer solution or suspension used in the cosmetic raw material of the present invention can be easily prepared by mixing silicone oil, organic oil, alcohol, or water with the vinyl polymer.
  • these liquids may be present during the polymerization of the vinyl polymer. In this case, it may be necessary to completely eliminate their odor by removing all residual unreacted vinyl monomers by subjecting the solution or dispersion to heat treatment under normal or reduced pressure.
  • pigments such as iron oxide and particles of inorganic oxides, such as titanium oxide, silicon oxide, mica, talc, etc., which are allowed to be used as cosmetic ingredients in cosmetic materials, can be compounded or combined with the solutions and dispersions.
  • surfactants may be added in order to improve the dispersibility of the vinyl polymer.
  • Such surfactants are exemplified by hexylbenzenesulfonic acid, octylbenzenesulfonic acid, decylbenzenesulfonic acid, dodecylbenzensulfonic acid, cetylbenzenesulfonic acid, myristylbenzenesulfonic acid, and their sodium salts and other anionic surfactants; octyltrimethylammonium hydroxide, dodecyltrimethylammonium hydroxide, hexadecyltrimethylarnmonium hydroxide, octyldimethylbenzylammonium hydroxide, decyldimethylbenzylammonium hydroxide, dioctadecyldimethylammonium hydroxide, tallow trimethylammonium hydroxide, coconut oil trimethylammonium
  • the average particle size of the vinyl polymer is preferably in the range of from 0.001 to 100 ⁇ m, and, even more preferably, in the range of from 0.01 to 50 ⁇ m. This is due to the fact that if the average particle size falls outside the indicated ranges, the feel produced on application by cosmetic products compounded with the polymer, and, in particular, finger and skin feel, as well as its spreadability, tend to be insufficient.
  • the cosmetic raw material of the present invention as described above is characterized by exhibiting superior stability in cosmetic products, imparting excellent feel on application and surface protective properties to cosmetic products, and, furthermore, improving their water repellency and oil repellency.
  • it when used in skin cosmetics, it has the advantage of superior water repellency, gas and moisture permeability, as well as the advantage of being unlikely to cause an unnatural, sticky skinfeel while imparting a clean and neat sensation, and, when used as a hair cosmetic material, has the advantage of imparting water repellency and hair-setting properties.
  • the cosmetic raw material of the present invention is suitable for use as a raw material for skin cosmetics and hair cosmetics.
  • the cosmetic product of the present invention is prepared by adding the above-mentioned cosmetic raw material and consists of the cosmetic raw material of the present invention and other cosmetic ingredients or raw materials.
  • the type etc. of the cosmetic product of the present invention so long as it is normally called a cosmetic product or cosmetic material.
  • skin cosmetic materials are exemplified by soaps, body shampoos, facial cleansing creams, and other cleansing cosmetic products; skin lotion, creams, cosmetic milk, packs, and other basic cosmetic products; face powders, foundations, and other base makeup cosmetic products, lipstick, cheek rouge, eye shadow, eyeliner, mascara, and other cosmetic products for the care of the eyes and eyebrows; nail polish, and other nail cosmetic products; depilating agents, shaving lotions, anti-perspirants and deodorants, sunburn preventives, and other special cosmetic products; perfumes, eau de cologne, and other scented cosmetic products.
  • the forms, in which the cosmetic product is used are exemplified by water base liquid formulations, oil base liquid formulations, milk formulations, creme formulations, foam formulations, semi-solid formulations, solid formulations, and powders.
  • the product can be atomized in spray form.
  • cosmetic raw materials forming part of the cosmetic product of the present invention are exemplified, for instance, by avocado oil, almond oil, olive oil, cacao butter, beef tallow, sesame oil, wheat germ oil, safflower oil, shea butter, turtle oil, camellia oil, persic oil, castor oil, rapeseed oil, macadamia nut oil, mink oil, egg yolk oil, Japanese wax, coconut oil, hydrogenated oil, and other oils and fats; orange roughy oil, camauba wax, candelilla wax, whale wax, jojoba oil, montan wax, beeswax, lanolin, and other waxes; liquid paraffin, Vaseline, paraffin, ceresin, microcrystalline wax, squalane, and other hydrocarbons; lauric acid, myristic acid, palmitic acid, stearic acid, oleic acid, behenic acid, undecylenic acid, oxystearic acid, linoleic acid, lanolinic
  • cured silicone particles can be also combined with the cosmetic product of the present invention.
  • Particles of resin-like cured silicone and rubber-like cured silicone are suggested as the above-mentioned cured silicone particles.
  • Resin-like cured silicone particles give a clean feel to the hair and skin while rubber-like cured product particles give an elastic feel to the skin.
  • Resin-like cured silicone particles are prepared by subjecting hydrolyzable silanes or their partial hydrolyzates to hydrolysis and condensation.
  • Rubber-like cured silicone particles are prepared by cross-linking cross-linkable silicone rubber compositions and then grinding the product into powder, or by dispersing cross- linkable silicone rubber compositions in a solvent such as water, etc., cross-linking it, and removing the solvent.
  • Water base suspensions of cured silicone rubber particles are preferable from the standpoint of the ease of compounding.
  • suggested techniques include dispersing rubber-like cured silicone particles in water using surface active agents etc. or dispersing cross-linkable silicone rubber compositions in water and then cross-linking them.
  • the amount of the added particles should be sufficient to make their content in the cosmetic product fall the range of from 0.1 to 99 wt%, and, more preferably, from 0.2 to 85 wt%.
  • the cosmetic raw material is also very useful in applications where it may be applied to skin in the form of a topical application, for example a patch, which may be used to deposit or apply a component to the skin.
  • suitable uses include the use as or in conjunction with a patch to apply cosmetic, or even active ingredients to the skin or via the skin to the body.
  • patches are known and have been described in the art together with ways of making and applying them, including for example EP 667382, in which ways of using materials as pressure sensitive adhesives for use as or in conjunction with patches have also been described.
  • the cosmetic raw material could be used for similar purposes, either alone or in conjunction with other suitable ingredients, which have been described in the art.
  • the cosmetic products of the present invention can be prepared by uniformly mixing the above-described cosmetic raw material of the present invention with other cosmetic raw materials.
  • Various mixers and kneaders commonly used in the preparation of cosmetic products can be utilized as mixing means.
  • Such equipment is exemplified, for instance, by Homo-Mixers, paddle mixers, Henschel mixers, Homo-Dispersers, colloid mixers, propeller agitators, Homogenizers, inline type continuous emulsifiers, ultrasonic emulsifiers, and vacuum kneaders.
  • viscosity refers to values obtained at 25°C.
  • evaluation of the characteristics of the cosmetic raw materials was carried out in accordance with the methods described below.
  • a vinyl polymer film on its surface was obtained by drying at room temperature to remove the solvent. A drop of water was placed on the surface of the coating film and the contact angle of the water drop was measured. An automatic contact angle meter (from Kyowa Interface Science Co., Ltd.) was used for measurement.
  • the glass transition temperature was measured using a differential scanning calorimeter (DSC).
  • a dispersion of the vinyl polymer containing 20 wt% of nonvolatile matter (hereinafter referred to as "cosmetic raw material (A)") was prepared by adding 80g cyclic dimethyl silicone (5-mer) to 20g of the thus obtained vinyl polymer having carbosiloxane dendritic structures and fluorinated organic groups. Its characteristics are listed in Table 1.
  • a dispersion of the vinyl polymer containing 20 wt% of nonvolatile matter (hereinafter referred to as "cosmetic raw material (C)") was prepared by adding 80g cyclic dimethyl silicone (5-mer) to 20g of the thus obtained vinyl polymer having carbosiloxane dendritic structures and fluorinated organic groups. Its characteristics are listed in Table 1.
  • a dispersion of the vinyl polymer containing 20 wt% of nonvolatile matter (hereinafter referred to as "cosmetic raw material (D)") was prepared by further adding 74.72g ethanol. Its characteristics are listed in Table 1.
  • a dispersion of the vinyl polymer containing 20 wt% of nonvolatile matter (hereinafter refe ⁇ ed to as "cosmetic raw material (E)") was prepared by adding 80g cyclic dimethyl silicone (5-mer) to 20g of the thus obtained vinyl polymer having carbosiloxane dendritic structures. Its characteristics are listed in Table 1.
  • the isopropyl alcohol solution of the vinyl polymer was subjected to 30-min. heat treatment at 140°C at a reduced pressure of 10 mm Hg to remove the isopropyl alcohol and unreacted monomer.
  • 3.68g triethanolamine was added thereto.
  • a dispersion of the vinyl polymer containing 20 wt% of nonvolatile matter (hereinafter refe ⁇ ed to as "cosmetic raw material (F)") was prepared by further adding 74.72g ethanol. Its characteristics are listed in Table 1.
  • an oil base liquid lipstick was prepared by further adding 0.1 parts by weight of an anti-oxidant, 0.1 parts by weight of fragrance, 2.0 parts by weight of silicone- treated titanium oxide, 2 parts by weight of Red No. 201, 1 part by weight of Red No. 202, and 3 parts by weight of Yellow No. 4 aluminum lake, uniformly mixing the ingredients, deaerating the mixture, and filling a container with it.
  • the thus obtained lipstick was evaluated in accordance with the methods described below. The results are shown in Table 2.
  • the results of the evaluation were represented in the following manner: cases, in which 8 to 10 people reported that the lipstick was easily spreadable, non-sticky, and produced a moisturized skinfeel, were designated as o, those, in which 4 to 7 people reported the same, were designated as ⁇ , and those, in which 3 or fewer people reported the same, were designated as x.
  • a group of 10 panelists applied the mascara to the eyelashes and evaluated its curling properties.
  • the results of the evaluation were represented in the following manner: cases, in which 8 to 10 people reported that the mascara exhibited curling properties, were designated as o, those, in which 4 to 7 people reported the same, were designated as ⁇ , and those, in which 3 or fewer people reported the same, were designated as x.
  • the results of the evaluation were represented in the following manner: cases, in which 8 to 10 people reported presence of remainders of mascara, were designated as o, those, in which 4 to 7 people reported the same, were designated as ⁇ , and those, in which 3 or fewer people reported the same, were designated as x.
  • a nail polish was prepared by uniformly mixing 40 parts by weight of cosmetic raw material (A), 15 parts by weight of nitrocellulose, 10 parts by weight of acetyl tributyl citrate, 2 parts by weight of camphor, 5 parts by weight of ethyl acetate, 10 parts by weight of butyl acetate, 16 parts by weight of toluene, 1 part by weight of organic bentonite, and 1 part by weight of pigment, and then filling a container with the mixture.
  • the thus obtained nail polish was evaluated in accordance with the methods described below. The results were listed in Table 4.
  • the results of the evaluation were represented in the following manner: cases, in which 8 to 10 people reported that the nail polish was easily spreadable and provided excellent smoothness, were designated as o, those, in which 4 to 7 people reported the same, were designated as ⁇ , and those, in which 3 or fewer people reported the same, were designated as x.
  • a skin cream cosmetic material was prepared by putting 15 parts by weight of cosmetic raw material (A), 2 parts by weight of silicone-treated titanium oxide powder, 10 parts by weight of octyl j9-methoxycinnamate, 12 parts by weight of a dimethylpolysiloxane with a viscosity of 20 mPa-s having both ends of the molecular chain blocked by trimethylsiloxy groups, 3 parts by weight of polyoxyethylene (40-mol adduct) hydrogenated castor oil, 60 parts by weight of squalane, 5 parts by weight of glycerin, 3 parts by weight of beeswax, a small amount of antiseptic, a small amount of fragrance, and an suitable amount of purified water in a Henschel mixer and stirring the ingredients for 10 minutes at 1500 rpm.
  • cosmetic raw material A
  • 2 parts by weight of silicone-treated titanium oxide powder 10 parts by weight of octyl j9-methoxycinnamate
  • the results of the evaluation were represented in the following manner: cases, in which 8 to 10 people reported that the cosmetic material was easily spreadable, did not produce an unpleasant sensation and produced an excellent skin feel, were designated as o, those, in which 4 to 7 people reported the same, were designated as ⁇ , and those, in which 3 or fewer people reported the same, were designated as x.
  • a group of 10 panelists applied the cream to the wrists, spreading and rubbing it in thoroughly with fingers, and performed work indoors for 8 hours at a temperature of 28 to 32°C and a humidity of 60% or higher. Subsequently, the presence/absence of remainders of adhered cream was evaluated after bending the wrists 50 times.
  • the results of the evaluation were represented in the following manner: cases, in which 8 to 10 people reported that there was some cream left, were designated as O, those, in which 4 to 7 people reported the same, were designated as ⁇ , and those, in which 3 or fewer people reported the same, were designated as x.
  • a shampoo was prepared by mixing 20 parts by weight of the disodium salt of sulfosuccinic acid monoester, 2 parts by weight of lauroyl diethanolamide, 5 parts by weight of cosmetic raw material (C), 0.2 parts by weight of fragrance, 0.1 parts by weight of antiseptic, 72.5 parts by weight of purified water, and a trace amount of colorant and filling a container with the mixture.
  • the thus obtained shampoo was evaluated in accordance with the methods described below. The results are shown in Table 6.
  • An aerosol hair spray was prepared by mixing 100 parts by weight of cosmetic raw material (D), 50 parts by weight of ethanol, and 35 parts by weight of liquefied petroleum gas under cooling conditions. The thus obtained hair spray was evaluated in accordance with the methods described below. The results are shown in Table 7.

Landscapes

  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Animal Behavior & Ethology (AREA)
  • Birds (AREA)
  • Epidemiology (AREA)
  • Emergency Medicine (AREA)
  • Dermatology (AREA)
  • Chemical & Material Sciences (AREA)
  • Dispersion Chemistry (AREA)
  • Cosmetics (AREA)
  • Compositions Of Macromolecular Compounds (AREA)
  • Silicon Polymers (AREA)

Abstract

A cosmetic raw material using a vinyl polymer containing carbosiloxane dendritic structures and fluorinated organic group as the main or most important ingredient, a cosmetic product obtained by compounding with the cosmetic raw material, and a method for manufacturing a cosmetic product, in which said cosmetic raw material is mixed with other cosmetic raw materials. The cosmetic raw material exhibits superior compounding stability in cosmetic products and capable of imparting excellent feel and surface protective properties to cosmetic products. The cosmetic product exhibits superior adhesion to the hair and skin.

Description

I
DESCRIPTION
Cosmetic raw material, cosmetic product, and method for manufacturing a cosmetic product
[0001]
The present invention relates to a cosmetic raw material, a cosmetic product, and a method for manufacturing a cosmetic product. Specifically, it relates to a cosmetic raw material exhibiting superior compounding stability in cosmetic products and capable of imparting excellent feel on application and surface protective properties to cosmetic products, to a cosmetic product obtained by compounding with the cosmetic raw material, and to a method for manufacturing the cosmetic product. Cosmetic where used herein includes the application to the body for purposes other than beautifying, such as administering of materials to skin.
[0002]
In the past, vinyl co-polymers of radical polymerizable monomers and organopolysiloxanes containing radical polymerizable groups have been known to be used as cosmetic raw materials. For instance, Japanese Patent Application Publication No. Hei 5-000924 offers a base oil for a hair dressing agent consisting of a vinyl polymer obtained by polymerizing methacrylic acid and tertiary butyl acrylate with a dimethylpolysiloxane oligomer containing methacrylic groups. While this vinyl co-polymer does give water repellent properties and slip to cosmetic products, its compatibility with other cosmetic raw materials is low, and its compounding stability is inferior. In addition, as a result of insufficient adhesion to the hair and skin, it easily washes off and has inferior surface protective properties. A cosmetic raw material using a vinyl polymer with carbosiloxane dendritic structures in side chains as its main ingredient has been proposed with a view to solve such problems (see EP 963751). However, the water repellency, oil repellency, skin- oil resistance, and adhesion to the hair and skin of such a vinyl polymer are still not completely satisfactory.
[0003] The inventors arrived at the present invention as a result of in-depth investigations aimed at overcoming the above-described problems. Namely, it is an object of the present invention to provide a cosmetic raw material exhibiting superior compounding stability in cosmetic products and capable of imparting excellent feel on application and surface protective properties to cosmetic products, a cosmetic product exhibiting superior adhesion to the hair and skin obtained by compounding with said cosmetic raw material, and a method for manufacturing the cosmetic product.
[0004] The present invention relates to a cosmetic raw material using a vinyl polymer containing carbosiloxane dendritic structures and fluorinated organic groups as its main or most important ingredient, a cosmetic product obtained by compounding with the cosmetic raw material, preferably by combining it with other raw materials or other cosmetic ingredients and a method for manufacturing the cosmetic product, in which the cosmetic raw material is mixed with other cosmetic ingredients or other raw materials.
[0005]
First of all, explanations are provided regarding the cosmetic raw material of the present invention. The vinyl polymer used in the cosmetic raw material of the present invention is characterized by containing carbosiloxane dendritic structures and fluorinated organic groups. Structures, in which vinylic polymerized units constitute the backbone and carbosiloxane dendritic structures along with fluorinated organic groups are attached in side chains, are particularly preferable. In this invention, the carbosiloxane dendritic structures are high molecular structures obtained by regular high-degree branching from a single silicon atom. Structures represented by the formula(I):
Figure imgf000003_0001
are suggested as a specific example (see EP1055674). In the formula(I), Z is a divalent organic group exemplified by alkylene, arylene, aralkylene, ester-containing divalent organic groups, ether-containing divalent organic groups, ketone-containing divalent organic groups, and amide-containing divalent organic groups. Among the above, organic groups represented by the following formulas are preferable.
Figure imgf000004_0001
where R9 is an alkylene group with 1 to 10 carbon atoms exemplified by methylene, ethylene, propylene, and butylene. Among the above, methylene and propylene are preferable. R10 is an alkyl group with 1 to 10 carbon atoms exemplified by methyl, ethyl, propyl, and butyl. Among the above, methyl is preferable. R1 ' is an alkylene group with 1 to 10 carbon atoms exemplified by methylene, ethylene, propylene, and butylene. Among the above, ethylene is preferable. The subscript «d» is an integer of 0 to 4, and «e» is 0 or 1. In the formula(I), the subscript «p» is 0 or 1. R1 is an aryl or alkyl group with 1 to 10 carbon atoms, with alkyl groups exemplified by methyl, ethyl, propyl, butyl, pentyl, isopropyl, isobutyl, cyclopentyl, and cyclohexyl groups, and aryl groups exemplified by phenyl and naphthyl groups. Among the above, methyl and phenyl are preferable, and methyl is particularly preferable. X1 is a silylalkyl group represented by the following formula(π) :
Figure imgf000004_0002
In the formula(π), R1 is the same as above. R2 is an alkylene group with 2 to 10 carbon atoms exemplified by ethylene, propylene, butylene, hexylene, and other linear alkylene groups; methylmethylene, methylethylene, 1-methylpentylene, 1,4-dimethylbutylene, and other branched alkylene groups. Among the above, ethylene, methylethylene, hexylene, 1- methylpentylene, and 1,4-dimethylbutylene are preferable. R3 is an alkyl group with 1 to 10 carbon atoms exemplified by methyl, ethyl, propyl, butyl, and isopropyl. Xl+1 is a group selected from the group comprising hydrogen atoms, aryl groups and alkyl groups with 1 to 10 carbon atoms, and the above-mentioned silylalkyl groups X1, with the alkyl and aryl groups exemplified by the same groups as the above-described R1. The superscript «i» is an integer of 1 to 10 indicating the generation of the silylalkyl group, starting in each carbosiloxane dendritic structure with a value of 1 for the X1 group in the formula(I), and «a'» is an integer of 0 to 3.
[0006] On the other hand, groups obtained by substituting fluorine atoms for some or all of the hydrogen atoms of methyl, ethyl, propyl, isopropyl, butyl, isobutyl, tert-butyl, pentyl, neopentyl, hexyl, cyclohexyl, heptyl, octyl, nonyl, decyl, undecyl, dodecyl, tridecyl, tetradecyl, hexadecyl, octadecyl, and other alkyl groups with 1 to 20 carbon atoms, as well as alkyloxyalkylene groups with 6 to 22 carbon atoms, are suggested as the fluorinated organic groups.
[0007]
Groups represented by the formula: -(CH2)x-(CF2)y-R13 are suggested as examples of fluoroalkyl groups obtained by substituting fluorine atoms for the hydrogen atoms of alkyl groups. In the formula, the subscript «x» is 0, 1, 2, or 3 and «y» is an integer of 1 to 20. R13 is an atom or group selected from a hydrogen atom, a fluorine atom, -CH(CF3)2- or -CF(CF3)2. Such fluorine-substituted alkyl groups are exemplified by linear or branched polyfluoroalkyl or perfluoroalkyl groups represented by the formulas shown below. -CF3, -C2F5, -nC3F7, -CF(CF3)2, -nC4F9, -CF2CF(CF3)2, -nC5F„, -nC6F13, -nC8F17, -CH2CF3, -CH(CF3)2, -CH2CH(CF3)2, -CH2(CF2)2F, -CH2(CF2)3F, -CH2(CF2)4F, -CH2(CF2)6F, -CH2(CF2)8F, -CH2CH2CF3, -CH2CH2(CF2)2F, -CH2CH2(CF2)3F, -CH2CH2(CF2)4F, -CH2CH2(CF2)6F, -CH2CH2(CF2)8F, -CH2CH2(CF2)10F, -CH2CH2(CF2)12F, -CH2CH2(CF2)14F, -CH2CH2(CF2)16F, -CH2CH2CH2CF3, -CH2CH2CH2(CF2)2F, -CH2CH2CH2(CF2)2H, -CH2(CF2)4H, and -CH2CH2(CF2)3H.
[0008] Groups represented by the general formula
-CH2CH2-(CF2)m-CFR14-[OCF2CF(CF3)]n-OC3F7 are suggested as fluoroalkyloxyfluoroalkylene groups obtained by substituting fluorine atoms for the hydrogen atoms of alkyloxyalkylene groups. In the formula, the subscript «m» is 0 or 1, «n» is 0, 1, 2, 3, 4, or 5, and R14 is a fluorine atom or CF3. Such fluoroalkyloxyfluoroalkylene groups are exemplified by perfluoroalkyloxyfluoroalkylene groups represented by the formulas shown below. -CH2CH2CF(CF3)-[OCF2CF(CF3)]n-OC3F7, -CH2CH2CF2CF2-[OCF2CF(CF3)]n-OC3F7.
[0009]
Fluoroalkyl groups in general, and fluoroalkyl groups with 1 to 14 carbon atoms in particular, are preferable among such fluorinated organic groups from the standpoint of improving the oil repellency and skin-oil resistance of the cosmetic raw material of the present invention. In addition, fluoroalkyl groups with 1 to 5 carbon atoms, and, more specifically, groups such as -CH2CF3, are preferable when it is desirable to reduce stickiness.
[0010]
To make compounding easier, the number average molecular weight of the vinyl polymer used in the present invention should preferably be between 3,000 and 2,000,000, and, even more preferably, between 5,000 and 800,000. In addition, the polymer can be used in various forms, for example, in liquid, rubber, paste, solid, or powder form. When compounding in a cosmetic product, it is preferable to use it in powder form or in the form of a suspension or solution prepared by dissolving in a solvent.
[0011]
This type of vinyl polymer is obtained by adding, if desired or necessary, (B) a vinyl monomer that does not have fluorinated organic groups in the molecule to (A) a vinyl monomer containing fluorinated organic groups in the molecule and (C) a carbosiloxane dendrimer containing radical polymerizable organic groups represented by the general formula(lTi):
Figure imgf000007_0001
wherein Y is a radical polymerizable organic group and R1 and X1 are the same as above and subjecting them to co-polymerization.
[0012] The vinyl monomers (A) containing fluorinated organic groups in the molecule are preferably monomers represented by the general formula: CH2=CR15COORf. In the formula, R is a hydrogen atom or methyl group, R is a fluorinated organic group exemplified by the above-described fluoroalkyl and fluoroalkyloxyfluoroalkylene groups.
Compounds represented by the formulas shown below are suggested as specific examples of Component (A). In the formulas shown below, «z» is an integer of 1 to 4.
CH2=CCH3COO-CF3 CH2=CCH3COO-C2F5 CH2=CCH3COO- nC3F7
CH2=CCH3COO-CF (CF3)2. CH2=CCH3COO- nC4F9
CH2=CCH3COO-CF 2 CF(CF3)2. CH2=CCH3COO- nCsFj i
CH2=CCH3COO- nC6F13. CH2=CCH3COO- nC8F17 CH2=CCH3COO-CH2CF3. CH2=CCH3COO-CH(CF3)2. CH2=CCH3COO-CH2CH(CF3)2
CH2=CCH3COO-CH2 (CF2)2F.
CH2=CCH3COO-CH2(CF2) 3F CH2=CCH3COO-CH2 (CF2)4F.
CH2=CCH3COO-CH2(CF2) 6F CH2=CCH3COO-CH2 (CF2)8F.
CH2=CCH3COO-CH2CH2CF3 CH2=CCH3COO-CH2CH2 (CF2)2F. CH2=CCH3COO-CH2CH2 (CF2)3F CH2=CCH3COO-CH2CH2 (CF2)4F.
CH2=CCH3COO-CH2CH2 (CF2)6F CH2=CCH3COO-CH2CH2 (CF2)8F.
CH2=CCH3COO-CH2CH2 (CF2)10F CH2=CCH3COO-CH2CH2 (CF2)12F.
CH2=CCH3COO-CH2CH2 (CF2)14F CH2=CCH3COO-CH2CH2 (CF2)16F.
CH2=CCH3COO-CH2CH2CH2CF3 CH2=CCH3COO-CH2CH2CH2 (CF2)2F. CH2=CCH3COO-CH2CH2CH2 (CF2 )2H CH2=CCH3COO-CH2 (CF2)4H.
CH2=CCH3COO-CH2CH2(CF2 )3H
CH2=CCH3COO-CH2CH2CF(CF3 )- [OCF2 CF(CF3 )]2 -OC3 F7.
CH2=CCH3COO-CH2CH2CF2CF2 - [OCF2 CF(CF3 )]z -OC3 F7. CH2=CHCOO-CF3. CH2=CHCOO-C2 F5. CH2=CHCOO-nC3F7. CH2=CHCOO-CF(CF3)2.
CH2=CHCOO-nC4F9. CH2=CHCOO- CF2CF(CF3)2. CH2=CHCOO-nC5Fπ.
CH2=CHCOO- nC6F13. CH2=CHCOO- nC8F17. CH2=CHCOO-CH2CF3.
CH2=CHCOO-CH(CF3)2. CH2=CHCOO-CH2CH(CF3)2. CH2=CHCOO-CH2(CF2)2F. CH2=CHCOO-CH2 (CF2)3 F. CH2=CHCOO-CH2(CF2)4 F. CH2=CHCOO-CH2(CF2)6F.
CH2=CHCOO-CH2 (CF2)8 F. CH2=CHCOO-CH2CH2CF3.
CH2=CHCOO-CH2CH2 (CF2)2F.
CH2=CHCOO-CH2CH2 (CF2)3F. CH2=CHCOO-CH2CH2 (CF2)4F.
CH2=CHCOO-CH2CH2 (CF2)6F. CH2=CHCOO-CH2CH2 (CF2)8F. CH2=CHCOO-CH2CH2(CF2)10F. CH2=CHCOO-CH2CH2 (CF2),2F.
CH2=CHCOO-CH2CH2 (CF2)MF. CH2=CHCOO-CH2CH2 (CF2)ι6F.
CH2=CHCOO-CH2CH2CH2CF3. CH2=CHCOO-CH2CH2 CH2 (CF2)2F.
CH2=CHCOO-CH2CH2CH2 (CF)2H. CH2=CHCOO-CH2(CF2)4H.
CH2=CHCOO-CH2CH2(CF2) 3H. CH2=CHCOO-CH2CH2CF(CF3)-[OCF2 CF(CF3 )]z -OC3 F7.
CH2=CHCOO-CH2CH2CF2CF2-[OCF2 CF(CF3 )]z -OC3 F7.
Among the above, vinyl polymers represented by the formulas shown below are preferable.
CH2=CHCOO-CH2CH2 (CF2)6F. CH2=CHCOO-CH2CH2 (CF2)8F.
CH2=CCH3COO-CH2CH2 (CF2)6 F. CH2=CCH3COO-CH2CH2 (CF2)8 F. CH2=CHCOO-CH2CF3. CH2=CCH3COO-CH2CF3
Vinyl polymers represented by the formulas shown below are particularly preferable.
CH2=CHCOO-CH2CF3. CH2=CCH3COO-CH2CF3.
[0013] The vinyl monomers (B) that do not contain fluorinated organic groups in the molecule may be any monomers having radical polymerizable vinyl groups, which are exemplified, for instance, by methyl acrylate, methyl methacrylate, ethyl acrylate, ethyl methacrylate, n- propyl acrylate, w-propyl methacrylate, isopropyl acrylate, isopropyl methacrylate, and other lower alkyl acrylates or methacrylates; glycidyl acrylate, glycidyl methacrylate; n- butyl acrylate, w-butyl methacrylate, isobutyl acrylate, isobutyl methacrylate, tert-butyl acrylate, tert-butyl methacrylate, «-hexyl acrylate, w-hexyl methacrylate, w-hexyl acrylate, n-hexyl methacrylate, cyclohexyl acrylate, cyclohexyl methacrylate, 2-ethylhexyl acrylate, 2-ethylhexyl methacrylate, octyl acrylate, octyl methacrylate, lauryl acrylate, lauryl methacrylate, stearyl acrylate, stearyl methacrylate, and other higher acrylates and methacrylates; vinyl acetate, vinyl propionate, and other lower fatty acid vinyl esters; vinyl butyrate, vinyl caproate, vinyl 2-ethylhexanoate, vinyl laurate, vinyl stearate, and other higher fatty acid esters; styrene, vinyltoluene, benzyl acrylate, benzyl methacrylate, phenoxyethyl acrylate, phenoxyethyl methacrylate, vinyl pyrrolidone, and other aromatic vinyl monomers; dimethyl aminoethyl acrylate, dimethyl aminoethyl methacrylate, diethyl aminoethyl acrylate, diethyl aminoethyl methacrylate, and other amino-containing vinyl monomers; acrylamide, methacrylamide, N-methylol acrylamide, N-methylol methacrylamide, N-methoxymethyl acrylamide, N-methoxymethyl methacrylamide, isobutoxymethoxyacrylamide, isobutoxymethoxymethacrylamide, N,N-dimethyl acrylamide, N,N-dimethyl methacrylamide, and other amide-containing vinyl monomers; hydroxyethyl acrylate, hydroxyethyl methacrylate, acrylic acid hydroxypropyl alcohol, methacrylic acid hydroxypropyl alcohol, and other hydroxyl-containing vinyl monomers; acrylic acid, methacrylic acid, itaconic acid, crotonic acid, fumaric acid, maleic acid, and other carboxylic acid-containing vinyl monomers; tetrahydrofurfuryl acrylate, tetrahydrofurfuryl methacrylate, butoxyethyl acrylate, butoxyethyl methacrylate, ethoxydiethylene glycol acrylate, ethoxydiethylene glycol methacrylate, polyethylene glycol acrylate, polyethylene glycol methacrylate, polypropylene glycol monoacrylate, polypropylene glycol monomethacrylate, hydroxybutyl vinyl ether, cetyl vinyl ether, 2- ethylhexyl vinyl ether, and other ether bond-containing vinyl monomers; acryloxypropyltrimethoxysilane, methacryloxypropyltrimethoxysilane, polydimethylsiloxanes containing acryl or methacryl groups at the one of the terminal ends, polydimethylsiloxanes containing alkenylaryl groups at the one of the terminal ends, and other unsaturated group-containing silicone compounds; butadiene; vinyl chloride; vinylidene chloride; acrylonitrile, methacrylonitrile; dibutyl fumarate; maleic anhydride; dodecyl succinic anhydride; acryl glycidyl ether, methacryl glycidyl ether, 3,4- epoxycyclohexylmethyl acrylate, 3,4-epoxycyclohexylmethyl methacrylate; alkali metal salts, ammonium salts, and organic amine salts of acrylic acid, methacrylic acid, itaconic acid, crotonic acid, fumaric acid, maleic acid, and other radical polymerizable unsaturated carboxylic acids, radical polymerizable unsaturated monomers containing sulfonic acid groups such as styrenesulfonic acid as well as their alkali metal salts, ammonium salts, and organic amine salts; quaternary ammonium salts derived from acrylic acid or methacrylic acid such as 2-hydroxy-3-methacryloxypropyl trimethylammonium chloride, methacrylic acid esters of a tertiary amine-containing alcohol such as methacrylic acid diethylamine ester and their quaternary ammonium salts.
[0014] In addition, it is also possible to use as vinyl monomers (B) polyfunctional vinyl monomers, which are exemplified, for instance, by trimethylolpropane triacrylate, trimethylolpropane trimethacrylate, pentaerythritol triacrylate, pentaerythritol trimethacrylate, ethylene glycol diacrylate, ethylene glycol dimethacrylate, tetraethylene glycol diacrylate, tetraethylene glycol dimethacrylate, polyethylene glycol diacrylate, polyethylene glycol dimethacrylate, 1,4-butanediol diacrylate, 1,4-butanediol dimethacrylate, 1,6-hexanediol diacrylate, 1,6-hexanediol dimethacrylate, neopentyl glycol diacrylate, neopentyl glycol dimethacrylate, trimethylolpropane trioxyethyl acrylate, trimethylolpropane trioxyethyl methacrylate, tris(2-hydroxyethyl)isocyanurate diacrylate, tris(2-hydroxyethyl)isocyanurate dimethacrylate, tris(2-hydroxyethyl)isocyanurate triacrylate, tris(2-hydroxyethyl)isocyanurate trimethacrylate, polydimethylsiloxane having both ends of the molecular chain blocked by alkenylaryl groups, and other unsaturated group-containing silicone compounds.
[0015] As concerns the above-mentioned ratio, in which component (A) and component (B) are co-polymerized, the weight ratio of component (A) to component (B) should be within the range of from 0.1:99.9 to 100:0, and, preferably, within the range of from 1:99 to 100:0.
[0016] The carbosiloxane dendrimer (C) is represented by the general formula(iπ), indicated above. In that formula(πT), Y is a radical polymerizable organic group, the type of which is not subject to any special limitations so long as this is an organic group capable of undergoing a radical addition reaction. Acryl and methacryl-containing organic groups, alkenylaryl-containing organic groups, or alkenyl groups with 2 to 10 carbon atoms represented by the general formulas shown below are suggested as specific examples.
Figure imgf000010_0001
Figure imgf000011_0001
In the formulas, R4 and R6 are hydrogen atoms or methyl groups, R5 and R are alkylene groups with 1 to 10 carbon atoms, and R7 is an alkyl group with 1 to 10 carbon atoms. The subscript «b» is an integer of 0 to 4, and «c» is 0 or 1. Acryloxymethyl, 3-acryloxypropyl, methacryloxymethyl, 3-methacryloxypropyl, 4-vinylphenyl, 3-vinylphenyl, 4-(2- propenyl)phenyl, 3-(2-propenyl)phenyl, 2-(4-vinylphenyl)ethyl, 2-(3-vinylphenyl)ethyl, vinyl, allyl, methallyl, and 5-hexenyl are suggested as examples of such radical polymerizable organic groups. The superscript «i» in the formula(II), which is an integer of 1 to 10, is the generation number of said silylalkyl group, in other words, the number of times the silylalkyl group is repeated. Thus, the carbosiloxane dendrimer of this component with a generation number of 1 is represented by the general formula:
Figure imgf000011_0002
(wherein Y, R , R , and R are the same as above, and R is a hydrogen atom or the same as R1 described above. The subscript «a'» is an integer of 0 to 3, the average total of «a!» per molecule being 0 to 7). Carbosiloxane dendrimers of this component with a generation number of 2 are represented by the general formula:
Figure imgf000011_0003
(wherein Y, R , R , R , and R are the same as above, and the subscripts «a » and «a » are integers of 0 to 3, the average total of «al» and «a2» per molecule being 0 to 25). Carbosiloxane dendrimers of this component with a generation number of 3 are represented by the general formula:
Figure imgf000012_0001
(wherein Y, R1, R2, R3, and R12 are the same as above and the subscripts «a'», «a2», and «a » are integers of 0 to 3, the average total of «a », «a », and «a » per molecule being 0 to 79).
[0017]
Component (C) is exemplified by carbosiloxane dendrimers represented by the average composition formulas shown below.
Figure imgf000013_0001
Figure imgf000014_0001
CH, CH3
CH2=CH-Si {OSi-C2H4-Si-(OSi-CH3)3}c
CH2 CH3 CH, CH,
CH2=CH-Si {OSi-C2H4-Si-(OSi-H) ' 33]J 3
CH CH,
[0018]
The carbosiloxane dendrimers of component (C) can be prepared using the preparation method for branched siloxane/silalkylene copolymers described in EP1055674. For example, they can be prepared by subjecting alkenyl-containing organic silicon compounds and silicon compounds containing silicon-bonded hydrogen atoms represented by the general formula:
Figure imgf000015_0001
(where R1 and Y are the same as above) to a hydrosilation reaction. For instance, 3- methacryloxypropyl tris(dimethylsiloxy)silane, 3-acryloxypropyl tris(dimethylsiloxy)silane, and 4-vinylphenyl tris(dimethylsiloxy)silane are used as the silicon compounds represented by the formula above. Vinyltris(trimethylsiloxy)silane, vinyltris(dimethylphenylsiloxy)silane, and 5-hexenyltris(trimethylsiloxy)silane are used as the alkenyl-containing organic silicon compounds. In addition, it is preferable to conduct the hydrosilation reaction in the presence of a transition metal catalyst, such as chloroplatinic acid and platinum/vinylsiloxane complex.
[0019]
The co-polymerization ratio of component (C), in terms of its weight ratio with respect to the total of component (A) and component (B), should be in the range of from 0.1 :99.9 to 99.9:0.1, preferably, in the range of from 1:99 to 99:1, and, even more preferably, in the range of from 5:95 to 95:5.
[0020] The vinyl polymers used in the present invention are prepared by co-polymerizing the above-described component (A), component (B), and component (C) or by polymerizing component (A) and component (C). Radical polymerization and ion polymerization can be used as the polymerization methods, with radical polymerization being preferable and solution polymerization being especially suitable. Solution polymerization is carried out by reacting the above-described components in a solvent in the presence of a radical initiator for 3 to 20 hours at a temperature of 50 to 150°C. Solvents used at such time are exemplified by hexane, octane, decane, cyclohexane, and other aliphatic hydrocarbons; benzene, toluene, xylene, and other aromatic hydrocarbons; diethyl ether, dibutyl ether, tetrahydrofuran, dioxane, and other ethers; acetone, methyl ethyl ketone, methyl isobutyl ketone, diisobutyl ketone, and other ketones; methyl acetate, ethyl acetate, butyl acetate, isobutyl acetate, and other esters; methanol, ethanol, isopropyl alcohol, butanol, and other alcohols; octamethylcyclotetrasiloxane, decamethylcyclopentasiloxane, hexamethyldisiloxane, octamethyltrisiloxane, and other organosiloxane oligomers. The radical initiators are publicly known conventional compounds used for radical polymerization, specifically exemplified by 2,2'-azobis(isobutyronitrile), 2,2'-azobis(2- methylbutyronitrile), 2,2'-azobis(2,4-dimethylvaleronitrile), and other azobis compounds; benzoyl peroxide, lauroyl peroxide, tert-butyl peroxybenzoate, tert-butyl peroxy-2- ethylhexanoate, and other organic peroxides. The radical initiators can be used singly or in combination as two or more initiators mixed together. The amount of the radical initiator is preferably in the range of from 0.1 to 5 parts by weight per 100 parts by weight of the total of the above-described component (A) to component (C). In addition, chain transfer agents can be added during polymerization. Specific example of the chain transfer agents include 2-mercaptoethanol, butylmercaptan, «-dodecylmercaptan, 3- mercaptopropyltrimethoxysilane, mercaptopropyl-containing polydimethylsiloxanes, and other mercapto compounds; methylene chloride, chloroform, carbon tetrachloride, butyl bromide, 3-chloropropyltrimethoxysilane, and other halogen compounds. In addition, after polymerization, it is preferable to remove residual unreacted vinyl monomers by treating the polymer under reduced pressure and heating.
[0021]
In addition, in order to further improve the adherence or adhesion of the vinyl polymer to the skin and hair, as well as impart it with suitable properties for easy washability after application, amino groups can be introduced in the side chains of the vinyl polymer by using, as part of component (B), vinyl monomers containing amino groups, such as dimethyl aminoethyl acrylate, dimethyl aminoethyl methacrylate, diethyl aminoethyl acrylate, and diethyl aminoethyl methacrylate, and then performing modification with potassium monochloroacetate, ammonium monochloroacetate, aminomethylpropanol salt of monochloroacetic acid, triethanolamine salt of monobromoacetic acid, sodium monochloropropionate, and other alkali metal salts of halogenated fatty acids; otherwise, carboxylic acid groups can be introduced in the side chains of the vinyl polymer by using, as part of component (B), vinyl monomers containing carboxylic acids, such as acrylic acid, methacrylic acid, itaconic acid, crotonic acid, fumaric acid, and maleic acid, etc., and then neutralizing the product with triethylamine, diethylamine, triethanolamine, and other amines.
[0022]
The cosmetic raw material of the present invention uses the above-described vinyl polymer containing carbosiloxane dendritic structures and fluorinated organic groups as its main or most important ingredient. Solutions or dispersions obtained by adding liquids selected from the group comprising silicone oil, organic oil, alcohol, and water to the vinyl polymer are suggested as examples of such materials. The viscosity of such a solution or dispersion at 25°C is preferably in the range of from 10 to 1,000,000,000 mPa-s, and, even more preferably, in particular, from the standpoint of improving the feel of the cosmetic product, in the range of from 100 to 500,000,000 mPa-s. In addition, the concentration of the vinyl polymer in the dispersion or solution is typically in the range of from 0.1 wt% to 95 wt%, and, preferably, in the range of from 1 wt% to 85 wt%. Furthermore, to make compounding and handling easier, it should preferably be in the range of from 5 wt% to 75 wt%.
[0023] Examples of the silicone oils include, for instance, dimethylpolysiloxane having both ends of the molecular chain blocked by trimethylsiloxy groups, dimethylsiloxane/methylphenylsiloxane copolymer having both ends of the molecular chain blocked by trimethylsiloxy groups, dimethylsiloxane/methyl(3,3,3- trifluoropropyl)siloxane copolymer having both ends of the molecular chain blocked by trimethylsiloxy groups, and other linear non-reactive silicone oils, as well as cyclic compounds such as hexamethylcyclotrisiloxane, octamethylcyclotetrasiloxane, decamethylcyclopentasiloxane, and dodecamethylcyclohexasiloxane. In addition to the above-mentioned non-reactive silicone oils, one may use modified polysiloxanes having polyether, amino, silanol, and other functional groups in the side chains or at the terminal ends of the molecular chain.
[0024] Examples of the organic oils include, for instance, liquid paraffin, isoparaffin, hexyl laurate, isopropyl myristate, myristyl myristate, cetyl myristate, 2-octyldodecyl myristate, isopropyl palmitate, 2-ethylhexyl palmitate, butyl stearate, decyl oleate, 2-octyldodecyl oleate, myristyl lactate, cetyl lactate, lanolin acetate, stearyl alcohol, oleyl alcohol, avocado oil, almond oil, olive oil, cacao butter, jojoba oil, sesame oil, soybean oil, Camellia oil, squalane, persic oil, castor oil, mink oil, cottonseed oil, coconut oil, egg yolk oil, beef tallow, pork fat, polypropylene glycol monooleate, neopentyl glycol-2-ethylhexanoate, and other glycol ether oils; isostearic acid triglyceride, coconut oil fatty acid triglyceride, and other polyhydric alcohol ester oils; polyoxyethylene lauryl ether, polyoxypropylene cetyl ether, and other polyoxyalkylene ether oils.
[0025]
Although any alcohols used in cosmetic raw materials may be utilized, methanol, ethanol, butanol, isopropyl alcohol, and other lower alcohols are preferable.
[0026]
The vinyl polymer solution or suspension used in the cosmetic raw material of the present invention can be easily prepared by mixing silicone oil, organic oil, alcohol, or water with the vinyl polymer. In addition, these liquids may be present during the polymerization of the vinyl polymer. In this case, it may be necessary to completely eliminate their odor by removing all residual unreacted vinyl monomers by subjecting the solution or dispersion to heat treatment under normal or reduced pressure. Moreover, pigments such as iron oxide and particles of inorganic oxides, such as titanium oxide, silicon oxide, mica, talc, etc., which are allowed to be used as cosmetic ingredients in cosmetic materials, can be compounded or combined with the solutions and dispersions. In addition, in case of dispersions, surfactants may be added in order to improve the dispersibility of the vinyl polymer. Such surfactants are exemplified by hexylbenzenesulfonic acid, octylbenzenesulfonic acid, decylbenzenesulfonic acid, dodecylbenzensulfonic acid, cetylbenzenesulfonic acid, myristylbenzenesulfonic acid, and their sodium salts and other anionic surfactants; octyltrimethylammonium hydroxide, dodecyltrimethylammonium hydroxide, hexadecyltrimethylarnmonium hydroxide, octyldimethylbenzylammonium hydroxide, decyldimethylbenzylammonium hydroxide, dioctadecyldimethylammonium hydroxide, tallow trimethylammonium hydroxide, coconut oil trimethylammonium hydroxide, and other cationic surfactants; nonionic surfactants based on polyoxyalkylene alkyl ethers, polyoxyalkylene alkyl phenols, polyoxyalkylene alkyl esters, polyoxyalkylene sorbitan esters, polyesters and ethylene oxide adducts of polyethylene glycol, polypropylene glycol, and diethylene glycol trimethylnonanol; as well as mixtures of two or more of the above surfactants. In such dispersions, the average particle size of the vinyl polymer is preferably in the range of from 0.001 to 100 μm, and, even more preferably, in the range of from 0.01 to 50 μm. This is due to the fact that if the average particle size falls outside the indicated ranges, the feel produced on application by cosmetic products compounded with the polymer, and, in particular, finger and skin feel, as well as its spreadability, tend to be insufficient.
[0027]
The cosmetic raw material of the present invention as described above is characterized by exhibiting superior stability in cosmetic products, imparting excellent feel on application and surface protective properties to cosmetic products, and, furthermore, improving their water repellency and oil repellency. In particular, when used in skin cosmetics, it has the advantage of superior water repellency, gas and moisture permeability, as well as the advantage of being unlikely to cause an unnatural, sticky skinfeel while imparting a clean and neat sensation, and, when used as a hair cosmetic material, has the advantage of imparting water repellency and hair-setting properties. In addition, because of its superior skin-oil resistance, it is characterized by significantly improving adhesion to the skin and hair. Thus, the cosmetic raw material of the present invention is suitable for use as a raw material for skin cosmetics and hair cosmetics.
[0028]
Next, explanations are provided regarding the cosmetic product of the present invention. In a preferred aspect of the invention, the cosmetic product of the present invention is prepared by adding the above-mentioned cosmetic raw material and consists of the cosmetic raw material of the present invention and other cosmetic ingredients or raw materials. There are no limitations concerning the type etc. of the cosmetic product of the present invention so long as it is normally called a cosmetic product or cosmetic material. Specifically, skin cosmetic materials, for instance, are exemplified by soaps, body shampoos, facial cleansing creams, and other cleansing cosmetic products; skin lotion, creams, cosmetic milk, packs, and other basic cosmetic products; face powders, foundations, and other base makeup cosmetic products, lipstick, cheek rouge, eye shadow, eyeliner, mascara, and other cosmetic products for the care of the eyes and eyebrows; nail polish, and other nail cosmetic products; depilating agents, shaving lotions, anti-perspirants and deodorants, sunburn preventives, and other special cosmetic products; perfumes, eau de cologne, and other scented cosmetic products. In addition, shampoos, hair rinses, hair treatments, permanent wave agents, hair dressing agents, hair-growing agents, hair tonics, hair dyes, etc. are suggested as hair cosmetic materials. Furthermore, toothpastes and bathing agents are suggested as other cosmetic products. The forms, in which the cosmetic product is used, are exemplified by water base liquid formulations, oil base liquid formulations, milk formulations, creme formulations, foam formulations, semi-solid formulations, solid formulations, and powders. In addition, the product can be atomized in spray form.
[0029]
Other cosmetic raw materials forming part of the cosmetic product of the present invention are exemplified, for instance, by avocado oil, almond oil, olive oil, cacao butter, beef tallow, sesame oil, wheat germ oil, safflower oil, shea butter, turtle oil, camellia oil, persic oil, castor oil, rapeseed oil, macadamia nut oil, mink oil, egg yolk oil, Japanese wax, coconut oil, hydrogenated oil, and other oils and fats; orange roughy oil, camauba wax, candelilla wax, whale wax, jojoba oil, montan wax, beeswax, lanolin, and other waxes; liquid paraffin, Vaseline, paraffin, ceresin, microcrystalline wax, squalane, and other hydrocarbons; lauric acid, myristic acid, palmitic acid, stearic acid, oleic acid, behenic acid, undecylenic acid, oxystearic acid, linoleic acid, lanolinic acid, synthetic fatty acids, and other higher fatty acids; ethyl alcohol, isopropyl alcohol, lauryl alcohol, cetyl alcohol, cetostearyl alcohol, stearyl alcohol, oleyl alcohol, behenyl alcohol, lanolin alcohol, hydrogenated lanolin alcohol, hexyl decanol, octyl dodecanol, isostearyl alcohol, and other alcohols; cholesterol, dihydrocholesterol, phytosterols, and other sterols; ethyl linoleate, isopropyl myristate, lanolin fatty acid isopropyl ester, hexyl laurate, myristyl myristate, cetyl myristate, octyl dodecyl myristate, decyl oleate, octyl dodecyl oleate, hexyl decyl dimethyloctanoate, glyceryl tri(caprylate/carprate), propylene glycol dioleate, glyceryl triisostearate, glyceryl triisooctanoate, cetyl lactate, myristyl lactate, diisostearyl maleate, and other fatty acid esters; glycerin, propylene glycol, 1,3-butylene glycol, polyethylene glycol, sodium d,l-pyrrolidonecarboxylate, sodium lactate, sorbitol, sodium hyaluronate, and other humectants; higher fatty acid soaps, sulfuric acid ester salts derived from higher alcohols, N-acyl glutamic acid salts, phosphoric acid ester salts, and other anionic surfactants; cationic surfactants; betaine, amino acid, imidazoline, lecithin-based, and other amphoteric surfactants; polyhydric alcohol ester-based, ethylene oxide condensation-type, and other nonionic surfactants, and other surfactants; iron oxides and other colored pigments; zinc oxides, titanium oxides, zirconium oxides, and other white pigments; mica, talc, cericite, and other skin-colored pigments; dimethylpolysiloxane, methylphenylpolysiloxane, octamethyltetracyclosiloxane, decamethylcyclopentasiloxane, polyether-modified silicone oils, amino-modified silicone oils, trimethylsilicic acid, and other silicone-based materials; purified water; carrageenan, alginic acid, alginic acid salts, gum arabic, traganth gum, pectin, agar-agar, casein, starch, xanthan gum, polyvinyl alcohol, polyvinyl pyrrolidine, poly(meth)acrylic acid and its salts, poly(meth)acrylic acid esters and their derivatives, polyethylene glycol, vinyl acetate resins, and other high molecular compounds; and, furthermore, thickening agents, gelling agents, anti-ageing agents, antistatic agents, pigment-moisturizing agents, dispersing agents, anti-fading agents, anti- precipitation agents, anti-sagging agents, UV absorbers, antibacterial agents, anti- inflammation agents, antiperspirants, antiseptics, perfumes, anti-oxidants, pH adjusting agents, aerosol agents, and cosmetic treatment components.
[0030]
In addition, cured silicone particles can be also combined with the cosmetic product of the present invention. Particles of resin-like cured silicone and rubber-like cured silicone are suggested as the above-mentioned cured silicone particles. Resin-like cured silicone particles give a clean feel to the hair and skin while rubber-like cured product particles give an elastic feel to the skin. Resin-like cured silicone particles are prepared by subjecting hydrolyzable silanes or their partial hydrolyzates to hydrolysis and condensation. Rubber-like cured silicone particles are prepared by cross-linking cross-linkable silicone rubber compositions and then grinding the product into powder, or by dispersing cross- linkable silicone rubber compositions in a solvent such as water, etc., cross-linking it, and removing the solvent. Water base suspensions of cured silicone rubber particles are preferable from the standpoint of the ease of compounding. As far as methods of manufacture are concerned, suggested techniques include dispersing rubber-like cured silicone particles in water using surface active agents etc. or dispersing cross-linkable silicone rubber compositions in water and then cross-linking them. In addition, the amount of the added particles should be sufficient to make their content in the cosmetic product fall the range of from 0.1 to 99 wt%, and, more preferably, from 0.2 to 85 wt%.
[0031]
Because of the particularly good adherence to skin, the cosmetic raw material is also very useful in applications where it may be applied to skin in the form of a topical application, for example a patch, which may be used to deposit or apply a component to the skin. Examples of suitable uses include the use as or in conjunction with a patch to apply cosmetic, or even active ingredients to the skin or via the skin to the body. Such patches are known and have been described in the art together with ways of making and applying them, including for example EP 667382, in which ways of using materials as pressure sensitive adhesives for use as or in conjunction with patches have also been described. The cosmetic raw material could be used for similar purposes, either alone or in conjunction with other suitable ingredients, which have been described in the art. The cosmetic products of the present invention can be prepared by uniformly mixing the above-described cosmetic raw material of the present invention with other cosmetic raw materials. Various mixers and kneaders commonly used in the preparation of cosmetic products can be utilized as mixing means. Such equipment is exemplified, for instance, by Homo-Mixers, paddle mixers, Henschel mixers, Homo-Dispersers, colloid mixers, propeller agitators, Homogenizers, inline type continuous emulsifiers, ultrasonic emulsifiers, and vacuum kneaders.
[0032]
[Application Examples]
Hereinbelow, the present invention is explained in detail by referring to application examples. In the examples, the word "viscosity" refers to values obtained at 25°C. In addition, the evaluation of the characteristics of the cosmetic raw materials was carried out in accordance with the methods described below.
[0033]
[Characteristics Of Cosmetic Raw Materials] • Water repellency
After coating the cosmetic raw material on a glass plate, a vinyl polymer film on its surface was obtained by drying at room temperature to remove the solvent. A drop of water was placed on the surface of the coating film and the contact angle of the water drop was measured. An automatic contact angle meter (from Kyowa Interface Science Co., Ltd.) was used for measurement.
• Skin-oil resistance
50 ml squalane was placed in a 100-ml beaker, whereupon a vinyl polymer film obtained in the same manner as described above was immersed therein overnight and subsequently subjected to visual assessment of changes in its external appearance. Cases, in which no changes were noted were designated as O, and cases, in which the coating film was swollen were designated as x.
• Glass transition temperature
The glass transition temperature was measured using a differential scanning calorimeter (DSC).
• Tactile sensation produced by coating films After coating the cosmetic raw material on a glass plate, a vinyl polymer film on its surface was obtained by drying at room temperature to remove the solvent. The tactile sensation produced by the surface of the coating film was evaluated by finger touch.
[0034] [Application Example 1]
43g methyl methacrylate, 17g H-butyl acrylate, lOg fluorinated organic group-containing vinyl monomer (1) represented by the formula:
Figure imgf000023_0001
30g carbosiloxane dendrimer represented by the formula:
Figure imgf000024_0001
1.5g 2,2'-azobis-2-methylbutyronitrile (from Otsuka Chemical Co., Ltd.), and lOOg toluene were placed in a 300-ml 4-necked flask fitted with an agitator, a temperature gauge, and a reflux tube and stirred for 6 hours under heating at 70 to 80°C in a nitrogen atmosphere. After stirring, the product of the reaction was analyzed using gas chromatography, which showed that a vinyl polymer had been obtained at a polymer conversion ratio of 97%. The toluene solution of the vinyl polymer was subjected to 30-min. heat treatment at 140°C at a reduced pressure of 10 mm Hg to remove the toluene and unreacted monomer. A dispersion of the vinyl polymer containing 20 wt% of nonvolatile matter (hereinafter referred to as "cosmetic raw material (A)") was prepared by adding 80g cyclic dimethyl silicone (5-mer) to 20g of the thus obtained vinyl polymer having carbosiloxane dendritic structures and fluorinated organic groups. Its characteristics are listed in Table 1.
[0035]
[Application Example 2] 23 g methyl methacrylate, 17g «-butyl acrylate, 30g fluorinated organic group-containing vinyl monomer (1) used in Application Example 1, 30g carbosiloxane dendrimer used in Application Example 1, 1.5g 2,2'-azobis-2-methylbutyronitrile (from Otsuka Chemical Co. Ltd.), and lOOg toluene were placed in a 300-ml 4-necked flask fitted with an agitator, a temperature gauge, and a reflux tube and stirred for 6 hours under heating at 70 to 80°C in a nitrogen atmosphere. After stirring, the product of the reaction was analyzed using gas chromatography, which showed that a vinyl polymer had been obtained at a polymer conversion ratio of 96%. The toluene solution of the vinyl polymer was subjected to 30- min. heat treatment at 140°C at a reduced pressure of 10 mm Hg to remove the toluene and unreacted monomer. A dispersion of the vinyl polymer containing 20 wt% of nonvolatile matter (hereinafter referred to as "cosmetic raw material (B)") was prepared by adding 80g cyclic dimethyl silicone (5-mer) to 20g of the thus obtained vinyl polymer having carbosiloxane dendritic structures and fluorinated organic groups. Its characteristics are listed in Table 1. [0036]
[Application Example 3]
43g methyl methacrylate, 17g w-butyl acrylate, lOg fluorinated organic group-containing vinyl monomer (2) represented by the formula:
Figure imgf000025_0001
30g carbosiloxane dendrimer used in Application Example 1, 1.5g 2,2'-azobis-2- methylbutyronitrile (from Otsuka Chemical Co., Ltd.), and lOOg toluene were placed in a 300-ml 4-necked flask fitted with an agitator, a temperature gauge, and a reflux tube and stiπed for 6 hours under heating at 70 to 80°C in a nitrogen atmosphere. After stirring, the product of the reaction was analyzed using gas chromatography, which showed that a vinyl polymer had been obtained at a polymer conversion ratio of 96%. The toluene solution of the vinyl polymer was subjected to 30-min. heat treatment at 140°C at a reduced pressure of 10 mm Hg to remove the toluene and unreacted monomer. A dispersion of the vinyl polymer containing 20 wt% of nonvolatile matter (hereinafter referred to as "cosmetic raw material (C)") was prepared by adding 80g cyclic dimethyl silicone (5-mer) to 20g of the thus obtained vinyl polymer having carbosiloxane dendritic structures and fluorinated organic groups. Its characteristics are listed in Table 1.
[0037]
[Application Example 4] 43g methyl methacrylate, 17g w-butyl acrylate, 15g methacrylic acid, lOg fluorinated organic group-containing vinyl monomer (1) used in Application Example 1, 15g carbosiloxane dendrimer used in Application Example 1, 1.5g 2,2'-azobis-2- methylbutyronitrile (from Otsuka Chemical Co., Ltd.), and lOOg isopropyl alcohol were placed in a 300-ml 4-necked flask fitted with an agitator, a temperature gauge, and a reflux tube and stirred for 6 hours under heating at 70 to 80°C in a nitrogen atmosphere. After stirring, the product of the reaction was analyzed using gas chromatography, which showed that a vinyl polymer had been obtained at a polymer conversion ratio of 95%. The isopropyl alcohol solution of the vinyl polymer was subjected to 30-min. heat treatment at 140°C at a reduced pressure of 10 mm Hg to remove the isopropyl alcohol and unreacted monomer. After adding 20g ethanol to 20g of the thus obtained vinyl polymer having carbosiloxane dendritic structures and fluorinated organic groups and making a dispersion, 3.68g triethanolamine was added thereto. Subsequently, a dispersion of the vinyl polymer containing 20 wt% of nonvolatile matter (hereinafter referred to as "cosmetic raw material (D)") was prepared by further adding 74.72g ethanol. Its characteristics are listed in Table 1.
[0038] [Comparative Example 1]
53g methyl methacrylate, 17g «-butyl acrylate, 30g carbosiloxane dendrimer used in Application Example 1, 1.5g 2,2'-azobis-2-methylbutyronitrile (from Otsuka Chemical Co., Ltd.), and lOOg toluene were placed in a 300-ml 4-necked flask fitted with an agitator, a temperature gauge, and a reflux tube and stirred for 6 hours under heating at 70 to 80°C in a nitrogen atmosphere. After stirring, the product of the reaction was analyzed using gas chromatography, which showed that a vinyl polymer had been obtained at a polymer conversion ratio of 97%. The toluene solution of the vinyl polymer was subjected to 30- min. heat treatment at 140°C at a reduced pressure of 10 mm Hg to remove the toluene and unreacted monomer. A dispersion of the vinyl polymer containing 20 wt% of nonvolatile matter (hereinafter refeπed to as "cosmetic raw material (E)") was prepared by adding 80g cyclic dimethyl silicone (5-mer) to 20g of the thus obtained vinyl polymer having carbosiloxane dendritic structures. Its characteristics are listed in Table 1.
[0039] [Comparative Example 2]
53g methyl methacrylate, 17g w-butyl acrylate, 15g methacrylic acid, 15g carbosiloxane dendrimer used in Application Example 1, 1.5g 2,2'-azobis-2-methylbutyronitrile (from Otsuka Chemical Co., Ltd.), and lOOg isopropyl alcohol were placed in a 300-ml 4-necked flask fitted with an agitator, a temperature gauge, and a reflux tube and stirred for 6 hours under heating at 70 to 80°C in a nitrogen atmosphere. After stirring, the product of the reaction was analyzed using gas chromatography, which showed that a vinyl polymer had been obtained at a polymer conversion ratio of 95%. The isopropyl alcohol solution of the vinyl polymer was subjected to 30-min. heat treatment at 140°C at a reduced pressure of 10 mm Hg to remove the isopropyl alcohol and unreacted monomer. After adding 20g ethanol to 20g of the thus obtained vinyl polymer having carbosiloxane dendritic structures and making a dispersion, 3.68g triethanolamine was added thereto. Subsequently, a dispersion of the vinyl polymer containing 20 wt% of nonvolatile matter (hereinafter refeπed to as "cosmetic raw material (F)") was prepared by further adding 74.72g ethanol. Its characteristics are listed in Table 1.
[0040]
[Table 1]
Figure imgf000027_0001
[0041]
[Application Example 5] <Lipstick>
55 parts by weight of cosmetic raw material (A), 20 parts by weight of a dimethylpolysiloxane with a viscosity of 2 mPa-s having both ends of the molecular chain blocked by trimethylsiloxy groups, 5 parts by weight of liquid lanolin, 3.8 parts by weight of castor oil, and 8 parts by weight of glyceryl triisostearate were mixed under heating at 85°C. After that, an oil base liquid lipstick was prepared by further adding 0.1 parts by weight of an anti-oxidant, 0.1 parts by weight of fragrance, 2.0 parts by weight of silicone- treated titanium oxide, 2 parts by weight of Red No. 201, 1 part by weight of Red No. 202, and 3 parts by weight of Yellow No. 4 aluminum lake, uniformly mixing the ingredients, deaerating the mixture, and filling a container with it. The thus obtained lipstick was evaluated in accordance with the methods described below. The results are shown in Table 2.
In addition, no changes in the external appearance of the lipstick were noted after allowing it to stand for 3 months at room temperature, which confirmed the excellent compounding stability of the cosmetic raw material of the present invention.
• Feel on application
A group of 10 panelists applied the lipstick to the lips and evaluated its spreadability, stickiness, and moisturizing feel produced. The results of the evaluation were represented in the following manner: cases, in which 8 to 10 people reported that the lipstick was easily spreadable, non-sticky, and produced a moisturized skinfeel, were designated as o, those, in which 4 to 7 people reported the same, were designated as Δ, and those, in which 3 or fewer people reported the same, were designated as x.
• Color transfer
After applying the lipstick to the lips, a group of 10 panelists pressed a piece of tissue paper to the lips for 5 seconds and evaluated the presence/absence of color transfer. The results of the evaluation were represented in the following manner: cases, in which 8 to 10 people reported that no traces of the lipstick were noticed on the tissue paper, were designated as o, those, in which 4 to 7 people reported the same, were designated as Δ, and those, in which 3 or fewer people reported the same, were designated as x.
• Long-term adhesion A group of 10 panelists applied the lipstick to the lips and performed work indoors for 8 hours at a temperature of 28 to 32°C and a humidity of 60% or higher, whereupon the presence/absence of remainders of lipstick on the lips was confirmed by finger touch. The results of the evaluation were represented in the following manner: cases, in which 8 to 10 people reported remainders of adhered lipstick, were designated as o, those, in which 4 to 7 people reported the same, were designated as Δ, and those, in which 3 or fewer people reported the same, were designated as x.
[0042]
[Application Example 6]
<Lipstick>
With the exception of using cosmetic raw material (B) instead of cosmetic raw material
(A) in Application Example 5, an oil base liquid lipstick was prepared in the same manner as in Application Example 5. The resultant lipstick was evaluated in the same manner as in Application Example 5, and the results were also listed in Table 2.
In addition, no changes in the external appearance of the lipstick were noted after allowing it to stand for 3 months at room temperature, which confirmed the excellent compounding stability of the cosmetic raw material of the present invention.
[0043]
[Comparative Example 3]
<Lipstick>
With the exception of using cosmetic raw material (E) instead of cosmetic raw material (A) in Application Example 5, an oil base liquid lipstick was prepared in the same manner as in
Application Example 5. The resultant lipstick was evaluated in the same manner as in
Application Example 5, and the results were also listed in Table 2.
[0044] [Table 2]
Application Example 5 Application Example 6 Comparative Example 3
Spreadability O O O
Stickiness O o o
Moisturized sensation o o o
Color transfer o o o
Long-term adhesion o O x
[0045] [Application Example 7] <Mascara>
62 parts by weight of cosmetic raw material (B), 15 parts by weight of a dextrin fatty acid ester and 4.5 parts by weight of low-boiling isoparaffin were added to 51 parts of isoparaffin under heating to prepare a dispersion, which was then mixed with 2 parts by weight of hydrophobic treated silicic anhydride, 1.5 parts by weight of organic bentonite, 7 parts by weight of black iron oxide powder, and 10 parts by weight of mica. Mascara was prepared by filling a container with the mixture. The thus obtained mascara was evaluated in accordance with the methods described below. The results were listed in Table 3. In addition, no changes in the external appearance of the mascara were noted after allowing it to stand for 3 months at room temperature, which confirmed the excellent compounding stability of the cosmetic raw material of the present invention.
• Feel on application A group of 10 panelists applied the mascara to the eyelashes and evaluated its spreadability. The results of the evaluation were represented in the following manner: cases, in which 8 to 10 people reported that the mascara was easily spreadable, were designated as o, those, in which 4 to 7 people reported the same, were designated as Δ, and those, in which 3 or fewer people reported the same, were designated as x.
• Curling properties
A group of 10 panelists applied the mascara to the eyelashes and evaluated its curling properties. The results of the evaluation were represented in the following manner: cases, in which 8 to 10 people reported that the mascara exhibited curling properties, were designated as o, those, in which 4 to 7 people reported the same, were designated as Δ, and those, in which 3 or fewer people reported the same, were designated as x.
• Long-term adhesion
A group of 10 panelists applied the mascara to the eyelashes and performed work indoors for 8 hours at a temperature of 28 to 32°C and a humidity of 60% or higher, whereupon the presence/absence of remainders of mascara was confirmed by finger touch. The results of the evaluation were represented in the following manner: cases, in which 8 to 10 people reported presence of remainders of mascara, were designated as o, those, in which 4 to 7 people reported the same, were designated as Δ, and those, in which 3 or fewer people reported the same, were designated as x.
[0046] [Comparative Example 4] <Mascara>
With the exception of using cosmetic raw material (E) instead of cosmetic raw material (B) in Application Example 7, mascara was prepared in the same manner as in Application Example 7. The resultant mascara was evaluated in the same manner as in Application Example 7, and the results were also listed in Table 3.
[0047] [Table 3]
Application Example 7 Comparative Example 4
Spreadability O o
Curling properties O o
Long-term adhesion o X
[0048]
[Application Example 8]
<Nail Polish>
A nail polish was prepared by uniformly mixing 40 parts by weight of cosmetic raw material (A), 15 parts by weight of nitrocellulose, 10 parts by weight of acetyl tributyl citrate, 2 parts by weight of camphor, 5 parts by weight of ethyl acetate, 10 parts by weight of butyl acetate, 16 parts by weight of toluene, 1 part by weight of organic bentonite, and 1 part by weight of pigment, and then filling a container with the mixture. The thus obtained nail polish was evaluated in accordance with the methods described below. The results were listed in Table 4.
In addition, no changes in the external appearance of the nail polish were noted after allowing it to stand for 3 months at room temperature, which confirmed the excellent compounding stability of the cosmetic raw material of the present invention. • Feel on application
A group of 10 panelists applied the nail polish to the fingernails and evaluated its spreadability and the smoothness of the film formed after drying. The results of the evaluation were represented in the following manner: cases, in which 8 to 10 people reported that the nail polish was easily spreadable and provided excellent smoothness, were designated as o, those, in which 4 to 7 people reported the same, were designated as Δ, and those, in which 3 or fewer people reported the same, were designated as x.
• Long-term adhesion A group of 10 panelists applied the nail polish to the fingernails and performed work indoors for 8 hours at a temperature of 28 to 32°C and a humidity of 60% or higher, whereupon the amount of remaimng adhered nail polish was evaluated by visual inspection. The results of the evaluation were represented in the following manner: cases, in which 8 to 10 people reported that the condition of the residual nail polish was the same as immediately upon application, were designated as o, those, in which 4 to 7 people reported the same, were designated as Δ, and those, in which 3 or fewer people reported the same, were designated as x.
• Water repellency The nail polish was applied to the fingernails of 10 panelists and dried, whereupon drops of water were placed on the fingernails and water repellency was evaluated based on the extent to which the water drops could stick to or were repelled by the surface. The results of the evaluation were represented in the following manner: cases, in which 8 to 10 people reported that the water drops were repelled by the nail polish, were designated as O, those, in which 4 to 7 people reported the same, were designated as Δ, and those, in which 3 or fewer people reported the same, were designated as x.
[0049]
[Application Example 9] <Nail Polish>
With the exception of using cosmetic raw material (C) instead of cosmetic raw material (A) in Application Example 8, a nail polish was prepared in the same manner as in Application Example 8. The resultant nail polish was evaluated in the same manner as in Application Example 8, and the results were also listed in Table 4.
[0050] [Comparative Example 5] <Nail Polish>
With the exception of using cosmetic raw material (E) instead of cosmetic raw material (A) in Application Example 8, a nail polish was prepared in the same manner as in Application Example 8. The resultant nail polish was evaluated in the same manner as in Application Example 8, and the results were also listed in Table 4.
[0051] [Table 4]
Application Example 8 Application Example 9 Comparative Example 5
Spreadability O O O
Coating film smoothness O o o
Long-term adhesion o O x
Water repellency o O Δ
[0052]
[Application Example 10]
<Skin Cream-Type Cosmetic Product>
A skin cream cosmetic material was prepared by putting 15 parts by weight of cosmetic raw material (A), 2 parts by weight of silicone-treated titanium oxide powder, 10 parts by weight of octyl j9-methoxycinnamate, 12 parts by weight of a dimethylpolysiloxane with a viscosity of 20 mPa-s having both ends of the molecular chain blocked by trimethylsiloxy groups, 3 parts by weight of polyoxyethylene (40-mol adduct) hydrogenated castor oil, 60 parts by weight of squalane, 5 parts by weight of glycerin, 3 parts by weight of beeswax, a small amount of antiseptic, a small amount of fragrance, and an suitable amount of purified water in a Henschel mixer and stirring the ingredients for 10 minutes at 1500 rpm. The thus obtained cosmetic material was evaluated in accordance with the methods described below. The results were listed in Table 5. In addition, no changes in the external appearance of the skin cream-type cosmetic material were noted after allowing it to stand for 3 months at room temperature, which confirmed the excellent compounding stability of the cosmetic raw material of the present invention.
• Feel on application
A group of 10 panelists applied the cream to the back of the hands and evaluated its spreadability and skin feel. The results of the evaluation were represented in the following manner: cases, in which 8 to 10 people reported that the cosmetic material was easily spreadable, did not produce an unpleasant sensation and produced an excellent skin feel, were designated as o, those, in which 4 to 7 people reported the same, were designated as Δ, and those, in which 3 or fewer people reported the same, were designated as x.
• Long-term adhesion
A group of 10 panelists applied the cream to the wrists, spreading and rubbing it in thoroughly with fingers, and performed work indoors for 8 hours at a temperature of 28 to 32°C and a humidity of 60% or higher. Subsequently, the presence/absence of remainders of adhered cream was evaluated after bending the wrists 50 times. The results of the evaluation were represented in the following manner: cases, in which 8 to 10 people reported that there was some cream left, were designated as O, those, in which 4 to 7 people reported the same, were designated as Δ, and those, in which 3 or fewer people reported the same, were designated as x.
• Water repellency
After applying and thoroughly spreading the cream on the backs of the hands of 10 panelists, the panelists washed hands with liquid soap and wiped them with a towel. After that, water drops were applied to the backs of the hands and water repellency was evaluated based on the extent to which the water drops could stick to or were repelled by the surface. The results of the evaluation were represented in the following manner: cases, in which 8 to 10 people reported that the water drops were repelled, were designated as O, those, in which 4 to 7 people reported the same, were designated as Δ, and those, in which 3 or fewer people reported the same, were designated as x.
[0053] [Comparative Example 6] <Skin Cream-Type Cosmetic Product>
With the exception of using cosmetic raw material (E) instead of 15 parts by weight of cosmetic raw material (A) in Application Example 10, a skin cream-type cosmetic material was prepared in the same manner as in Application Example 10. The cream-type cosmetic material was evaluated in the same manner as in Application Example 10, and the results were also listed in Table 5.
[0054] [Table 5]
Application Example 10 Comparative Example 6
Spreadability O Δ
Skin feel O O
Long-term adhesion O x
Water repellency O Δ
[0055]
[Application Example 11] <Shampoo>
A shampoo was prepared by mixing 20 parts by weight of the disodium salt of sulfosuccinic acid monoester, 2 parts by weight of lauroyl diethanolamide, 5 parts by weight of cosmetic raw material (C), 0.2 parts by weight of fragrance, 0.1 parts by weight of antiseptic, 72.5 parts by weight of purified water, and a trace amount of colorant and filling a container with the mixture. The thus obtained shampoo was evaluated in accordance with the methods described below. The results are shown in Table 6.
• Post-washing assessment
The gloss and luster of hair was visually evaluated by 10 panelists after washing the hair with the shampoo and drying it. The results of the evaluation were represented in the following manner: cases, in which 8 to 10 people reported that the hair was glossy and lustrous, were designated as o, those, in which 4 to 7 people reported the same, were designated as Δ, and those, in which 3 or fewer people reported the same, were designated as x. • Long-term adhesion
The presence/absence of residual shampoo was evaluated by 10 panelists by finger touch after washing the hair with the shampoo and drying it. The results of the evaluation were represented in the following manner: cases, in which 8 to 10 people reported presence of residual adhered shampoo, were designated as O, those, in which 4 to 7 people reported the same, were designated as Δ, and those, in which 3 or fewer people reported the same, were designated as x.
• Water repellency
After washing the hair with the shampoo and drying it, 10 panelists evaluated water repellency by spraying water drops on the hair and assessing how well the water drops were repelled by the hair. The results of the evaluation were represented in the following manner: cases, in which 8 to 10 people reported good water repellency, were designated as o, those, in which 4 to 7 people reported the same, were designated as Δ, and those, in which 3 or fewer people reported the same, were designated as x.
[0056]
[Comparative Example 7] <Shampoo>
With the exception of using 5 parts by weight of cosmetic raw material (E) instead of cosmetic raw material (C) in Application Example 11 , a shampoo was prepared in the same manner as in Application Example 11. The shampoo was evaluated in the same manner as in Application Example 11, and the results were also listed in Table 6.
[0057] [Table 6]
Application Example 11 Comparative Example 7
Gloss and luster after washing hair O O
Long-term adhesion O X
Water repellency o Δ [0058]
[Application Example 12] <Hair Spray>
An aerosol hair spray was prepared by mixing 100 parts by weight of cosmetic raw material (D), 50 parts by weight of ethanol, and 35 parts by weight of liquefied petroleum gas under cooling conditions. The thus obtained hair spray was evaluated in accordance with the methods described below. The results are shown in Table 7.
• Hair gloss and luster 10 panelists had their hair sprayed with the hair spray and styled. After setting, the gloss and luster of the hair were visually evaluated. The results of the evaluation were represented in the following manner: cases, in which 8 to 10 people reported that the hair was glossy and lustrous, were designated as O, those, in which 4 to 7 people reported the same, were designated as Δ, and those, in which 3 or fewer people reported the same, were designated as x.
• Hair set retention properties
After curling the hair, it was treated with the hair spray. After wearing a wet towel for 5 minutes, 10 panelists evaluated curl retention. The results of the evaluation were represented in the following manner: cases, in which 8 to 10 people reported curl retention, were designated as o, those, in which 4 to 7 people reported the same, were designated as Δ, and those, in which 3 or fewer people reported the same, were designated as x.
• Long-term adhesion 10 panelists had their hair sprayed with the hair spray and styled, and, after setting, performed work indoors for 8 hours at a temperature of 28 to 32°C and a humidity of 60% or higher. Subsequently, the presence/absence of residual hair spray was confirmed by finger touch. The results of the evaluation were represented in the following manner: cases, in which 8 to 10 people reported presence of adhered hair spray, were designated as o, those, in which 4 to 7 people reported the same, were designated as Δ, and those, in which 3 or fewer people reported the same, were designated as x.
[0059] [Comparative Example 8] <Hair Spray>
With the exception of using cosmetic raw material (F) instead of cosmetic raw material (D) in Application Example 12, a hair spray was prepared in the same manner as in Application Example 12. The hair spray was evaluated in the same manner as in Application Example 12, and the results were also listed in Table 7.
[0060] [Table 7]
Application Example 12 Comparative Example 8
Hair gloss and luster O o
Hair set retention properties O
Long-term adhesion o

Claims

1. A cosmetic raw material, wherein a vinyl polymer containing carbosiloxane dendritic structures and fluorinated organic groups is used as the main or most important ingredient.
2. The cosmetic raw material according to Claim 1, wherein the carbosiloxane dendritic structures are groups represented by the formula(I):
Figure imgf000039_0001
wherein Z is a divalent organic group, «p» is 0 or 1, R1 is an aryl or alkyl group with 1 to 10 carbon atoms and X1 is a silylalkyl group represented by the following formula(π):
Figure imgf000039_0002
wherein R1 is the same as above, R2 is an alkylene group with 2 to 10 carbon atoms, R3 is an alkyl group with 1 to 10 carbon atoms, and X1+1 is a group selected from the group comprising hydrogen atoms, aryl groups and alkyl groups with up to 10 carbon atoms, and silylalkyl groups X1, wherein superscript «i» is an integer of 1 to 10 indicating the generation of the silylalkyl group starting in each carbosiloxane dendritic structure with a value of 1 for the X1 group in the formula(ι), and the subscript «a'» is an integer of 0 to 3
3. The cosmetic raw material according to Claim 2, wherein the vinyl polymer is a copolymer of: (A) vinyl monomers containing fluorinated organic groups in the molecule,
(B) optionally vinyl monomers that do not have fluorinated organic groups in the molecule, and (C) carbosiloxane dendrimers, having radical polymerizable organic groups, represented by the general formula(rfl):
Figure imgf000040_0001
wherein Y is a radical polymerizable organic group, R , 11 : i-s an aryl or alkyl group with 1 to 10 carbon atoms, and X1 is a silylalkyl group represented by the following formula(π)
Figure imgf000040_0002
wherein R is the same as above, R is an alkylene group with 2 to 10 carbon atoms, R is an alkyl group with 1 to 10 carbon atoms, and X1+1 is a group selected from the group comprising hydrogen atoms, aryl groups and alkyl groups with 1 to 10 carbon atoms, and the above-mentioned silylalkyl groups X1, wherein superscript «i» is an integer of 1 to 10 indicating the generation of said silylalkyl group, starting in each carbosiloxane dendritic structure with a value of 1 for the X1 group in the formula(rπ), and the subscript «a'» is an integer of 0 to 3, said vinyl polymer having a co-polymerization ratio of component (A) to component (B) of 0.1 to 100 : 99.9 to 0 wt%, and a co-polymerization ratio of the total of component (A) and component (B) to component (C) of 0.1 to 99.9 : 99.9 to 0.1 wt%.
4. The cosmetic raw material according to Claim 3, wherein the radical polymerizable organic group Y in component (C) is a group selected from the group comprising organic groups containing acrylic or methacrylic groups represented by the general formula:
Figure imgf000040_0003
wherein R is a hydrogen atom or methyl, and R is an alkylene group with 1 to 10 carbon atoms or
Figure imgf000041_0001
wherein R and R are as defined above, organic groups containing alkenylaryl groups represented by the general formula:
Figure imgf000041_0002
wherein R6 is a hydrogen atom or methyl, R7 is an alkyl group with 1 to 10 carbon atoms, R8 is an alkylene group with 1 to 10 carbon atoms, «b» is an integer of 0 to 4, and «c» is 0 or 1, and alkenyl groups with 2 to 10 carbon atoms.
5. The cosmetic raw material according to Claim 1, which is a solution or dispersion comprising the vinyl polymer containing carbosiloxane dendritic structures and fluorinated organic groups, and a liquid selected from the group comprising silicone oil, organic oil, alcohol, and water.
6. A cosmetic product obtained by compounding with the cosmetic raw material according to any one of Claims 1 to 5.
7. A cosmetic product according to Claim 6, which is intended for topical application to skin.
8. A method for manufacturing a cosmetic product, in which a cosmetic raw material according to any one of Claims 1 to 5 is mixed with other raw materials.
PCT/JP2002/012400 2001-11-28 2002-11-27 Cosmetic raw material, cosmetic product, and method for manufacturing a cosmetic product Ceased WO2003045337A2 (en)

Priority Applications (4)

Application Number Priority Date Filing Date Title
US10/496,022 US7488492B2 (en) 2001-11-28 2002-11-27 Cosmetic raw material cosmetic product and method for manufacturing a cosmetic product
EP02791950A EP1448154B1 (en) 2001-11-28 2002-11-27 Cosmetic raw material, cosmetic product, and method for manufacturing a cosmetic product
AU2002361070A AU2002361070A1 (en) 2001-11-28 2002-11-27 Cosmetic raw material, cosmetic product, and method for manufacturing a cosmetic product
DE60222579T DE60222579T2 (en) 2001-11-28 2002-11-27 COSMETIC STARTING PRODUCT, COSMETIC COMPOSITION AND METHOD FOR PRODUCING A COSMETIC COMPOSITION

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
JP2001361948 2001-11-28
JP2001-361948 2001-11-28
JP2002054679A JP4693330B2 (en) 2001-11-28 2002-02-28 Cosmetic raw materials, cosmetics and methods for producing cosmetics
JP2002-54679 2002-02-28

Publications (2)

Publication Number Publication Date
WO2003045337A2 true WO2003045337A2 (en) 2003-06-05
WO2003045337A3 WO2003045337A3 (en) 2004-02-19

Family

ID=26624727

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/JP2002/012400 Ceased WO2003045337A2 (en) 2001-11-28 2002-11-27 Cosmetic raw material, cosmetic product, and method for manufacturing a cosmetic product

Country Status (7)

Country Link
US (1) US7488492B2 (en)
EP (1) EP1448154B1 (en)
JP (1) JP4693330B2 (en)
AT (1) ATE373463T1 (en)
AU (1) AU2002361070A1 (en)
DE (1) DE60222579T2 (en)
WO (1) WO2003045337A2 (en)

Cited By (77)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2867974A1 (en) * 2004-03-26 2005-09-30 Oreal DETERGENT COSMETIC COMPOSITION COMPRISING A PERIPHERAL FATTY DENDRIFER, A SURFACTANT AND A COSMETIC AGENT, AND USES THEREOF
WO2005092275A1 (en) * 2004-03-26 2005-10-06 L'oreal Cosmetic composition comprising a dendritic polymer with peripheral fatty chains, a surfactant and a cosmetic agent, and uses thereof
WO2006058793A1 (en) * 2004-12-03 2006-06-08 L'oréal Cosmetic composition comprising a vinyl polymer containing at least one carbosiloxane dendrimer-based unit
FR2878738A1 (en) * 2004-12-03 2006-06-09 Oreal COSMETIC COMPOSITION COMPRISING A VINYL POLYMER HAVING AT LEAST ONE DERIVE DERIVATIVE OF CARBOSILOXANE DENDRIMER.
EP1862162A1 (en) * 2006-05-31 2007-12-05 L'Oréal Cosmetic composition comprising a vinyl polymer and an olefin copolymer
WO2009080960A3 (en) * 2007-12-05 2009-12-17 L'oreal Cosmetic make-up and/or care method using a siloxane resin and a film-forming polymer
FR2935269A1 (en) * 2008-09-04 2010-03-05 Oreal COSMETIC COMPOSITION COMPRISING A POLYMER WITH A DENDRIMERIC CARBOSILOXANE MOTIF.
WO2010063964A2 (en) 2008-12-02 2010-06-10 L'oreal Cosmetic composition for making-up and/or caring for keratin materials and make-up method
WO2011051323A2 (en) 2009-10-29 2011-05-05 L'oreal Makeup and/or care composition containing pigments coated with a fluoro compound and a vinyl polymer containing a carbosiloxane dendrimer-based unit
CN102056588A (en) * 2008-06-11 2011-05-11 花王株式会社 Cosmetic
WO2011073294A1 (en) 2009-12-18 2011-06-23 L'oreal Cosmetic composition comprising a supramolecular compound capable of establishing hydrogen bonds, and a particular additional ingredient
WO2011147696A1 (en) 2010-05-26 2011-12-01 L'oreal Cosmetic composition comprising an oil and a polymer both bearing a hydrogen-bond-generating joining group, and cosmetic treatment process
WO2011148328A2 (en) 2010-05-26 2011-12-01 L'oreal Cosmetic process for making-up and/or caring for the skin and/or the lips
WO2011147697A1 (en) 2010-05-26 2011-12-01 L'oreal Cosmetic composition comprising a polysiloxane and a polymer both bearing a hydrogen-bond-generating joining group, and cosmetic treatment process
WO2012001173A1 (en) 2010-07-02 2012-01-05 L'oreal Method of filling skin imperfections
WO2012027144A1 (en) 2010-08-23 2012-03-01 Dow Corning Corporation Emulsions containing saccharide siloxane copolymer emulsifiers and methods for their preparation and use
WO2012027145A1 (en) 2010-08-23 2012-03-01 Dow Corning Corporation Emulsions containing saccharide siloxane copolymer emulsifiers and methods for their preparation and use
WO2012027143A1 (en) 2010-08-23 2012-03-01 Dow Corning Corporation Saccharide siloxane copolymers and methods for their preparation and use
WO2012131083A1 (en) 2011-04-01 2012-10-04 L'oreal Composition comprising perlite and a polymer bearing a carbosiloxane dendrimer-based unit
WO2012143344A1 (en) 2011-04-22 2012-10-26 L'oreal Compositions containing a polymer with a carbosiloxane dendrimer unit and a large amount of monoalcohol
US20130046028A1 (en) * 2010-04-29 2013-02-21 Dow Corning Toray Co., Ltd. Cosmetic Raw Material
WO2014083175A1 (en) 2012-11-30 2014-06-05 L'oreal Cosmetic water-in-oil emulsion, in particular packaged in aerosol form, comprising at least one vinyl polymer containing at least one carbosiloxane dendrimer-based unit, at least one olefin copolymer and at least one antiperspirant active agent
WO2014087183A1 (en) 2012-12-04 2014-06-12 L'oreal Solid powdery cosmetic composition
WO2014154701A2 (en) 2013-03-25 2014-10-02 L'oreal Lipstick composition in emulsion form comprising a particular film-forming polymer and treatment process employing same
US8871229B2 (en) 2012-02-28 2014-10-28 L'oreal Cosmetic composition for long-wearing properties
US9000051B2 (en) 2010-05-26 2015-04-07 L'oreal Cosmetic composition based on a supramolecular polymer and an absorbent filler
WO2015092632A2 (en) 2013-12-20 2015-06-25 L'oreal Cosmetic composition comprising a polymer bearing a carbosiloxane dendrimer unit and expanded polymer particles
WO2016030842A1 (en) 2014-08-28 2016-03-03 L'oreal Gel-type cosmetic composition with improved staying power
WO2016030840A1 (en) 2014-08-28 2016-03-03 L'oreal Readily removable gel-type cosmetic composition
WO2016030837A1 (en) 2014-08-28 2016-03-03 L'oreal Non-tacky gel-type cosmetic composition with improved wear property
WO2016083387A1 (en) 2014-11-24 2016-06-02 L'oreal Synthetic phyllosilicate in powder form as a mattifying and/or application homogenising agent
WO2016083385A1 (en) 2014-11-24 2016-06-02 L'oreal Hydroalcoholic or aqueous gel of synthetic phyllosilicates as a thickening, mattifying and/or application homogenising agent
WO2016096627A1 (en) 2014-12-18 2016-06-23 L'oreal Composition comprising polymer particles, a hydrocarbon-based oil and a silicone resin, and process using the same
WO2017050782A1 (en) 2015-09-25 2017-03-30 L'oreal Assembly for packaging and applying a liquid cosmetic product
WO2017050992A1 (en) 2015-09-25 2017-03-30 L'oreal Liquid cosmetic composition comprising a high non-volatile oil content and lip treatment process
WO2017050958A1 (en) 2015-09-25 2017-03-30 L'oreal Liquid cosmetic composition comprising a high non-volatile oil content and a non-ionic silicone surfactant, and lip treatment process
WO2017167669A1 (en) 2016-03-31 2017-10-05 L'oreal Device for applying a composition in the form of an emulsion comprising a film-forming agent and non-volatile oils
WO2017167667A1 (en) 2016-03-31 2017-10-05 L'oreal Aqueous emulsion comprising a silicone-based dendritic polymer, a silicone gum and a semi-crystalline polymer or a wax and treatment of the lips
WO2017167668A1 (en) 2016-03-31 2017-10-05 L'oreal Device for packaging and applying an emulsion comprising a film-forming agent and non-volatile oils and composition
WO2018122014A1 (en) 2016-12-29 2018-07-05 L'oreal Superhydrophobic cosmetic composition in aerosol form
WO2018228783A1 (en) 2017-06-15 2018-12-20 L'oreal Water-in-oil emulsion based on non-thickening, non-interference fillers, on a nonvolatile oil, on a hydrophobic film-forming polymer, on and emulsifying silicone elastomer and on pigments
EP3578160A1 (en) 2015-12-17 2019-12-11 L'oreal Composition of gel/gel type based on hydrophobic coated pigments and a glycol compound
FR3088201A1 (en) 2018-11-13 2020-05-15 L'oreal COMPOSITION COMPRISING POLYMER PARTICLES, A VOLATILE HYDROCARBON OIL, A FILM-FORMING SILICONE VINYL POLYMER, A PHENYLATED SILICONE NON-VOLATILE OIL
WO2020176281A1 (en) 2019-02-28 2020-09-03 L'oreal Skin perfecting cosmetic compositions and methods of use
WO2021132734A1 (en) 2019-12-24 2021-07-01 L'oreal Composition comprising spherical hydrophobic silica aerogel and silicone polymer
KR20210150441A (en) * 2019-04-01 2021-12-10 다우 도레이 캄파니 리미티드 Copolymer having carbosiloxane dendrimer structure and composition containing same, cosmetic raw material, film former and cosmetic
FR3111556A1 (en) 2020-06-18 2021-12-24 L'oreal Composition comprising polymer particles, a volatile hydrocarbon-based oil, a film-forming silicone vinyl polymer, a coconut oil
WO2022026282A1 (en) 2020-07-31 2022-02-03 L'oreal Skin tightening cosmetic compositions and methods of use
FR3114026A1 (en) 2020-09-16 2022-03-18 L'oreal SKIN PERFECTION COSMETIC COMPOSITIONS and METHODS OF USE
FR3117833A1 (en) 2020-12-21 2022-06-24 L'oreal Three-step makeup process comprising on the one hand a basic amino acid and on the other hand an acid dye and kit
FR3117832A1 (en) 2020-12-21 2022-06-24 L'oreal Two-step makeup process comprising on the one hand an amino acid and on the other hand an acid dye and kit
WO2022146701A1 (en) 2020-12-29 2022-07-07 L'oreal Skin perfecting cosmetic compositions and methods of use
WO2022146700A1 (en) 2020-12-29 2022-07-07 L'oreal Skin perfecting compositions and methods of use
FR3120196A1 (en) 2021-03-01 2022-09-02 L'oreal SKIN PERFECTION COSMETIC COMPOSITIONS AND METHODS OF USE
WO2022199974A1 (en) 2021-03-26 2022-09-29 L'oreal Emulsion with neutralized water-soluble screening agent, nonvolatile nonphenylated silicone oil, film-forming polymer and linear polyoxyalkylenated polydimethylmethylsiloxane emulsifier
FR3121600A1 (en) 2021-04-08 2022-10-14 L'oreal SKIN PERFECTION COSMETIC COMPOSITIONS AND METHODS OF USE
WO2023275500A1 (en) 2021-07-02 2023-01-05 L V M H Recherche Cosmetic make-up composition
WO2023094277A1 (en) 2021-11-26 2023-06-01 L'oreal Cosmetic water-in-oil emulsion comprising a specific water-soluble uv screening agent, a base, a volatile oil, a hydrophobic film-forming polymer, a polyoxyalkylenated linear polydimethylmethylsiloxane and a vitamin b3
WO2023118530A1 (en) 2021-12-23 2023-06-29 L'oreal Cosmetic composition comprising a polyhydroxyalkanoate copolymer bearing a(n) (un)saturated hydrocarbon-based chain and a silicone polymer
US11696880B2 (en) 2019-12-31 2023-07-11 L'oreal Skin tightening compositions and methods of use
WO2023208802A1 (en) 2022-04-28 2023-11-02 L'oreal Makeup processes using a polyphenol and at least one polyglycerol compound, and compositions for performing the process
WO2023208806A1 (en) 2022-04-28 2023-11-02 L'oreal Makeup process with the application of a composition comprising a polyphenol and a polyoxyalkylenated compound, and a dyestuff, followed by the application of an anhydrous or emulsified composition
FR3134988A1 (en) 2022-04-28 2023-11-03 L'oreal Make-up process with the application of a composition comprising a polyphenol and a polyoxyalkylenated and/or polyglycerolated compound, and a coloring material then application of a composition in the form of an emulsion
FR3134989A1 (en) 2022-04-28 2023-11-03 L'oreal Makeup process with the application of a composition comprising a polyphenol and a polyoxyalkylene compound, and a coloring material then application of an anhydrous composition
FR3152122A3 (en) 2023-08-17 2025-02-21 L'oreal COMPOSITION IN THE FORM OF A WATER-IN-OIL EMULSION AND ASSOCIATED PROCESSES
FR3152982A1 (en) 2023-09-20 2025-03-21 L'oreal Solid composition in powder form comprising a film-forming polymer in the solid state.
FR3152981A1 (en) 2023-09-20 2025-03-21 L'oreal Process for preparing a cosmetic composition comprising a powdery phase and a film-forming polymer solubilized in a volatile solvent; pigment formulation.
FR3154006A1 (en) 2023-10-16 2025-04-18 L'oreal Low water W/O emulsion comprising a hydrophobic film-forming polymer, a linear silicone polyol, hyaluronic acid, vitamin B3 and a xanthic base
FR3154317A3 (en) 2023-10-18 2025-04-25 L'oreal EMULSION COMPOSITIONS CONTAINING A CARBOSILOXANE DENDRIMER COMPOUND AND A WATER-BASED FILM FORMER
FR3156036A1 (en) 2023-11-30 2025-06-06 L'oreal INVERT LIQUID EMULSION WITH A FILM-FORMING SILICONE POLYMER, OPTIONALLY A TITANIUM DIOXIDE-BASED PIGMENT AND BORON NITRIDE PARTICLES
WO2025132142A1 (en) 2023-12-20 2025-06-26 L'oreal Invert emulsion comprising pullulan, an apolar hydrocarbon-based oil, a silicone film-forming polymer and a dyestuff, and makeup process
FR3158227A1 (en) 2024-01-17 2025-07-18 L'oreal Cosmetic water-in-oil emulsion comprising a volatile oil, a hydrophobic film-forming polymer, a polyoxyalkylenated linear polydimethylmethylsiloxane and a vitamin B3.
WO2026008495A1 (en) 2024-07-02 2026-01-08 L V M H Recherche Glossy, transfer-resistant anhydrous composition
WO2026008482A1 (en) 2024-07-02 2026-01-08 L V M H Recherche Glossy, solid, anhydrous, transfer-free composition
WO2026008483A1 (en) 2024-07-02 2026-01-08 L V M H Recherche Glossy anhydrous non-transfer liquid composition
FR3164120A1 (en) 2024-07-02 2026-01-09 L V M H Recherche Glossy, transfer-proof formula
WO2026082628A1 (en) 2024-10-18 2026-04-23 L'oreal Composition comprising a polyester and a lipophilic silicone polymer

Families Citing this family (30)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1545434B1 (en) * 2002-07-23 2009-12-02 E-L Management Corp. Transfer resistant cosmetic
TW200505493A (en) * 2003-05-26 2005-02-16 Shiseido Co Ltd Emulsified composition for hair
EP1907068B1 (en) 2005-06-21 2011-09-07 Dow Corning Toray Co., Ltd. Gelling agent comprising a modified organopolysiloxane
US8034891B2 (en) 2006-05-19 2011-10-11 Dow Corning Toray Company, Ltd. Polyether-modified organopolysiloxane, diorganopolysiloxane-polyether block copolymer, their production methods, and cosmetic preparation
JP5383035B2 (en) 2007-12-27 2014-01-08 東レ・ダウコーニング株式会社 Process for producing amino acid-modified organopolysiloxane emulsion
JP5389821B2 (en) * 2007-12-28 2014-01-15 ロレアル Cosmetic composition containing a polar modified wax and a tackifier
JP5666773B2 (en) * 2008-12-16 2015-02-12 株式会社 資生堂 Cosmetics
CN102686646B (en) * 2009-12-24 2015-08-19 道康宁东丽株式会社 Surface treatment agent for powder used in cosmetics and cosmetics containing powder treated with the surface treatment agent
CN102665668B (en) * 2009-12-24 2014-10-22 道康宁东丽株式会社 Copolymer having carbosiloxane dendrimer structure, and composition and cosmetic containing the same
JP5046405B2 (en) * 2010-03-05 2012-10-10 信越化学工業株式会社 Fluorine-containing organopolysiloxane composition and method for producing the same
JP5624455B2 (en) 2010-12-24 2014-11-12 東レ・ダウコーニング株式会社 Polysiloxane-N, N-dihydrocarbylene sugar-modified multiblock copolymer and method for producing the same
JP2012136587A (en) 2010-12-24 2012-07-19 Dow Corning Toray Co Ltd Polysiloxane-hydrocarbylene aminohydrocarbylene multiblock copolymer and method for producing the same
JP5833821B2 (en) * 2010-12-28 2015-12-16 東レ・ダウコーニング株式会社 Additive for coating agent and coating agent containing the same
JP5976456B2 (en) * 2012-08-22 2016-08-23 花王株式会社 Cosmetics
JP6092545B2 (en) * 2012-08-22 2017-03-08 東レ・ダウコーニング株式会社 Copolymer having carbosiloxane dendrimer structure and hydrophilic group and use thereof
JP5797618B2 (en) 2012-08-22 2015-10-21 東レ・ダウコーニング株式会社 Copolymer having carbosiloxane dendrimer structure, and composition and cosmetic containing the same
WO2015097110A1 (en) * 2013-12-23 2015-07-02 L'oreal Solid composition with a vinyl polymer bearing a carbosiloxane dendrimer unit, volatile hydrocarbon-based oils and solid fatty alcohol, and treatment process
WO2015097103A1 (en) * 2013-12-23 2015-07-02 L'oreal Solid composition with a vinyl polymer bearing a carbosiloxane dendrimer unit and two incompatible phenyl silicone oils, and treatment process
CA2940203C (en) * 2014-04-25 2019-08-06 Novartis Ag Carbosiloxane vinylic monomers
JP6192632B2 (en) * 2014-12-11 2017-09-06 株式会社 資生堂 Cosmetics
EP3646850A4 (en) * 2017-06-28 2021-03-31 Dow Toray Co., Ltd. FILM MAKERS FOR COSMETICS AND COSMETICS WITH IT
WO2019003897A1 (en) * 2017-06-28 2019-01-03 東レ・ダウコーニング株式会社 Copolymer having carbosiloxane dendrimer structure and acidic group, composition containing same, and cosmetic
JP6875256B2 (en) * 2017-11-10 2021-05-19 信越化学工業株式会社 How to make cosmetics
CN113164793B (en) * 2018-12-12 2024-05-17 陶氏环球技术有限责任公司 Polymer blends for personal care formulations
WO2022093497A1 (en) 2020-10-28 2022-05-05 Dow Silicones Corporation Silicon -(meth)acrylate copolymer and methods for its preparation and use in personal care compositions
WO2022108856A1 (en) * 2020-11-17 2022-05-27 Dow Global Technologies Llc Fixative polymer for hair styling
EP4265657A4 (en) * 2020-12-21 2024-11-27 Dow Toray Co., Ltd. Radical copolymer composition, production method therefor, and cosmetic or cosmetic ingredient containing radical copolymer composition
EP4265652A4 (en) * 2020-12-21 2024-12-11 Dow Toray Co., Ltd. Monomer composition and method for producing same, and cosmetic or cosmetic raw material including monomer composition
KR20250003711A (en) 2022-04-13 2025-01-07 다우 글로벌 테크놀로지스 엘엘씨 Silicone-vinyl ester functional compounds and their preparation methods and uses in personal care compositions
KR20250116679A (en) * 2022-11-30 2025-08-01 다우 도레이 캄파니 리미티드 Molded solid particles composed of thermoplastic copolymers and a method for producing the same, and a cosmetic comprising the same

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0835091A4 (en) * 1995-06-26 1999-08-04 Revlon Consumer Prod Corp Glossy transfer resistant cosmetic compositions
US6280748B1 (en) * 1998-06-12 2001-08-28 Dow Corning Toray Silicone, Ltd. Cosmetic raw material cosmetic product and method for manufacturing cosmetic products
JP4493746B2 (en) * 1998-11-30 2010-06-30 東レ・ダウコーニング株式会社 Coating material
JP2001139413A (en) * 1999-11-10 2001-05-22 Daikin Ind Ltd Cosmetic powder treated with fluorocopolymer
US6342209B1 (en) * 2000-05-04 2002-01-29 Revlon Consumer Products Corporation Cosmetic compositions containing film forming polymers plasticized with esters and malic acid
AU2002211435A1 (en) * 2000-10-05 2002-04-15 Societe L'oreal S.A. Concordantly uv-photoprotecting and artificial tanning compositions

Cited By (103)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2005092275A1 (en) * 2004-03-26 2005-10-06 L'oreal Cosmetic composition comprising a dendritic polymer with peripheral fatty chains, a surfactant and a cosmetic agent, and uses thereof
FR2867974A1 (en) * 2004-03-26 2005-09-30 Oreal DETERGENT COSMETIC COMPOSITION COMPRISING A PERIPHERAL FATTY DENDRIFER, A SURFACTANT AND A COSMETIC AGENT, AND USES THEREOF
WO2006058793A1 (en) * 2004-12-03 2006-06-08 L'oréal Cosmetic composition comprising a vinyl polymer containing at least one carbosiloxane dendrimer-based unit
FR2878738A1 (en) * 2004-12-03 2006-06-09 Oreal COSMETIC COMPOSITION COMPRISING A VINYL POLYMER HAVING AT LEAST ONE DERIVE DERIVATIVE OF CARBOSILOXANE DENDRIMER.
EP1862162A1 (en) * 2006-05-31 2007-12-05 L'Oréal Cosmetic composition comprising a vinyl polymer and an olefin copolymer
FR2901698A1 (en) * 2006-05-31 2007-12-07 Oreal COSMETIC COMPOSITION COMPRISING VINYL POLYMER AND OLEFIN COPOLYME
US8828372B2 (en) 2006-05-31 2014-09-09 L'oreal Cosmetic composition comprising at least one vinyl polymer and at least one olefin copolymer
WO2009080960A3 (en) * 2007-12-05 2009-12-17 L'oreal Cosmetic make-up and/or care method using a siloxane resin and a film-forming polymer
CN102056588A (en) * 2008-06-11 2011-05-11 花王株式会社 Cosmetic
CN102056588B (en) * 2008-06-11 2013-11-06 花王株式会社 Cosmetic
US8541009B2 (en) 2008-06-11 2013-09-24 Kao Corporation Cosmetic
WO2010026538A1 (en) * 2008-09-04 2010-03-11 L'oreal Cosmetic composition containing a polymer comprising a carbosiloxane dendrimer unit
US10905640B2 (en) 2008-09-04 2021-02-02 L'oreal Cosmetic composition containing a polymer comprising a carbosiloxane dendrimer unit
US10646421B2 (en) 2008-09-04 2020-05-12 L'oreal Cosmetic composition containing a polymer comprising a carbosiloxane dendrimer unit
FR2935269A1 (en) * 2008-09-04 2010-03-05 Oreal COSMETIC COMPOSITION COMPRISING A POLYMER WITH A DENDRIMERIC CARBOSILOXANE MOTIF.
WO2010063964A2 (en) 2008-12-02 2010-06-10 L'oreal Cosmetic composition for making-up and/or caring for keratin materials and make-up method
WO2010063965A2 (en) 2008-12-02 2010-06-10 L'oreal Cosmetic composition for making-up and/or caring for keratin material and make-up method
WO2011051323A2 (en) 2009-10-29 2011-05-05 L'oreal Makeup and/or care composition containing pigments coated with a fluoro compound and a vinyl polymer containing a carbosiloxane dendrimer-based unit
WO2011073294A1 (en) 2009-12-18 2011-06-23 L'oreal Cosmetic composition comprising a supramolecular compound capable of establishing hydrogen bonds, and a particular additional ingredient
US20130046028A1 (en) * 2010-04-29 2013-02-21 Dow Corning Toray Co., Ltd. Cosmetic Raw Material
WO2011147697A1 (en) 2010-05-26 2011-12-01 L'oreal Cosmetic composition comprising a polysiloxane and a polymer both bearing a hydrogen-bond-generating joining group, and cosmetic treatment process
US9000051B2 (en) 2010-05-26 2015-04-07 L'oreal Cosmetic composition based on a supramolecular polymer and an absorbent filler
WO2011148328A2 (en) 2010-05-26 2011-12-01 L'oreal Cosmetic process for making-up and/or caring for the skin and/or the lips
US10335361B2 (en) 2010-05-26 2019-07-02 L'oreal Cosmetic process for making-up and/or caring for the skin and/or the lips
WO2011147696A1 (en) 2010-05-26 2011-12-01 L'oreal Cosmetic composition comprising an oil and a polymer both bearing a hydrogen-bond-generating joining group, and cosmetic treatment process
WO2012001173A1 (en) 2010-07-02 2012-01-05 L'oreal Method of filling skin imperfections
WO2012027143A1 (en) 2010-08-23 2012-03-01 Dow Corning Corporation Saccharide siloxane copolymers and methods for their preparation and use
WO2012027145A1 (en) 2010-08-23 2012-03-01 Dow Corning Corporation Emulsions containing saccharide siloxane copolymer emulsifiers and methods for their preparation and use
WO2012027144A1 (en) 2010-08-23 2012-03-01 Dow Corning Corporation Emulsions containing saccharide siloxane copolymer emulsifiers and methods for their preparation and use
WO2012131083A1 (en) 2011-04-01 2012-10-04 L'oreal Composition comprising perlite and a polymer bearing a carbosiloxane dendrimer-based unit
WO2012143344A1 (en) 2011-04-22 2012-10-26 L'oreal Compositions containing a polymer with a carbosiloxane dendrimer unit and a large amount of monoalcohol
US8871229B2 (en) 2012-02-28 2014-10-28 L'oreal Cosmetic composition for long-wearing properties
WO2014083175A1 (en) 2012-11-30 2014-06-05 L'oreal Cosmetic water-in-oil emulsion, in particular packaged in aerosol form, comprising at least one vinyl polymer containing at least one carbosiloxane dendrimer-based unit, at least one olefin copolymer and at least one antiperspirant active agent
US10660827B2 (en) 2012-12-04 2020-05-26 L'oreal Solid powdery cosmetic composition
WO2014087183A1 (en) 2012-12-04 2014-06-12 L'oreal Solid powdery cosmetic composition
EP3593863A1 (en) 2013-03-25 2020-01-15 L'oreal Lipstick composition in emulsion form comprising a particular film-forming polymer and treatment process employing same
WO2014154701A2 (en) 2013-03-25 2014-10-02 L'oreal Lipstick composition in emulsion form comprising a particular film-forming polymer and treatment process employing same
WO2015092632A2 (en) 2013-12-20 2015-06-25 L'oreal Cosmetic composition comprising a polymer bearing a carbosiloxane dendrimer unit and expanded polymer particles
WO2016030842A1 (en) 2014-08-28 2016-03-03 L'oreal Gel-type cosmetic composition with improved staying power
WO2016030840A1 (en) 2014-08-28 2016-03-03 L'oreal Readily removable gel-type cosmetic composition
WO2016030837A1 (en) 2014-08-28 2016-03-03 L'oreal Non-tacky gel-type cosmetic composition with improved wear property
WO2016083385A1 (en) 2014-11-24 2016-06-02 L'oreal Hydroalcoholic or aqueous gel of synthetic phyllosilicates as a thickening, mattifying and/or application homogenising agent
WO2016083387A1 (en) 2014-11-24 2016-06-02 L'oreal Synthetic phyllosilicate in powder form as a mattifying and/or application homogenising agent
WO2016096627A1 (en) 2014-12-18 2016-06-23 L'oreal Composition comprising polymer particles, a hydrocarbon-based oil and a silicone resin, and process using the same
WO2017050782A1 (en) 2015-09-25 2017-03-30 L'oreal Assembly for packaging and applying a liquid cosmetic product
WO2017050992A1 (en) 2015-09-25 2017-03-30 L'oreal Liquid cosmetic composition comprising a high non-volatile oil content and lip treatment process
WO2017050958A1 (en) 2015-09-25 2017-03-30 L'oreal Liquid cosmetic composition comprising a high non-volatile oil content and a non-ionic silicone surfactant, and lip treatment process
EP3578160A1 (en) 2015-12-17 2019-12-11 L'oreal Composition of gel/gel type based on hydrophobic coated pigments and a glycol compound
WO2017167668A1 (en) 2016-03-31 2017-10-05 L'oreal Device for packaging and applying an emulsion comprising a film-forming agent and non-volatile oils and composition
WO2017167669A1 (en) 2016-03-31 2017-10-05 L'oreal Device for applying a composition in the form of an emulsion comprising a film-forming agent and non-volatile oils
WO2017167667A1 (en) 2016-03-31 2017-10-05 L'oreal Aqueous emulsion comprising a silicone-based dendritic polymer, a silicone gum and a semi-crystalline polymer or a wax and treatment of the lips
WO2018122014A1 (en) 2016-12-29 2018-07-05 L'oreal Superhydrophobic cosmetic composition in aerosol form
WO2018228783A1 (en) 2017-06-15 2018-12-20 L'oreal Water-in-oil emulsion based on non-thickening, non-interference fillers, on a nonvolatile oil, on a hydrophobic film-forming polymer, on and emulsifying silicone elastomer and on pigments
FR3088201A1 (en) 2018-11-13 2020-05-15 L'oreal COMPOSITION COMPRISING POLYMER PARTICLES, A VOLATILE HYDROCARBON OIL, A FILM-FORMING SILICONE VINYL POLYMER, A PHENYLATED SILICONE NON-VOLATILE OIL
WO2020176281A1 (en) 2019-02-28 2020-09-03 L'oreal Skin perfecting cosmetic compositions and methods of use
KR20210150441A (en) * 2019-04-01 2021-12-10 다우 도레이 캄파니 리미티드 Copolymer having carbosiloxane dendrimer structure and composition containing same, cosmetic raw material, film former and cosmetic
EP3950727A4 (en) * 2019-04-01 2022-12-07 Dow Toray Co., Ltd. COPOLYMER HAVING CARBOSILOXANE DENDRIME STRUCTURE, AND COMPOSITION, COSMETIC INGREDIENT, COATING FORMING AGENT AND COSMETIC PRODUCT CONTAINING THE SAME
KR102908051B1 (en) 2019-04-01 2026-01-07 다우 도레이 캄파니 리미티드 Copolymer having a carbosiloxane dendrimer structure and composition containing the same, cosmetic raw material, film-forming agent and cosmetic
WO2021132734A1 (en) 2019-12-24 2021-07-01 L'oreal Composition comprising spherical hydrophobic silica aerogel and silicone polymer
US11696880B2 (en) 2019-12-31 2023-07-11 L'oreal Skin tightening compositions and methods of use
FR3111556A1 (en) 2020-06-18 2021-12-24 L'oreal Composition comprising polymer particles, a volatile hydrocarbon-based oil, a film-forming silicone vinyl polymer, a coconut oil
WO2022026282A1 (en) 2020-07-31 2022-02-03 L'oreal Skin tightening cosmetic compositions and methods of use
FR3114026A1 (en) 2020-09-16 2022-03-18 L'oreal SKIN PERFECTION COSMETIC COMPOSITIONS and METHODS OF USE
FR3117832A1 (en) 2020-12-21 2022-06-24 L'oreal Two-step makeup process comprising on the one hand an amino acid and on the other hand an acid dye and kit
FR3117833A1 (en) 2020-12-21 2022-06-24 L'oreal Three-step makeup process comprising on the one hand a basic amino acid and on the other hand an acid dye and kit
WO2022146700A1 (en) 2020-12-29 2022-07-07 L'oreal Skin perfecting compositions and methods of use
WO2022146701A1 (en) 2020-12-29 2022-07-07 L'oreal Skin perfecting cosmetic compositions and methods of use
FR3120196A1 (en) 2021-03-01 2022-09-02 L'oreal SKIN PERFECTION COSMETIC COMPOSITIONS AND METHODS OF USE
WO2022199974A1 (en) 2021-03-26 2022-09-29 L'oreal Emulsion with neutralized water-soluble screening agent, nonvolatile nonphenylated silicone oil, film-forming polymer and linear polyoxyalkylenated polydimethylmethylsiloxane emulsifier
FR3121044A1 (en) 2021-03-26 2022-09-30 L'oreal Emulsion with neutralized water-soluble filter, non-volatile non-phenyl silicone oil, film-forming polymer and linear polyoxyalkylenated polydimethylmethylsiloxane emulsifier
FR3121600A1 (en) 2021-04-08 2022-10-14 L'oreal SKIN PERFECTION COSMETIC COMPOSITIONS AND METHODS OF USE
WO2023275500A1 (en) 2021-07-02 2023-01-05 L V M H Recherche Cosmetic make-up composition
FR3124730A1 (en) 2021-07-02 2023-01-06 L V M H Recherche Makeup cosmetic composition
FR3129598A1 (en) 2021-11-26 2023-06-02 L'oreal Cosmetic water-in-oil emulsion comprising a particular water-soluble UV filter, a base, a volatile oil, a hydrophobic film-forming polymer, a polyoxyalkylenated linear polydimethylmethylsiloxane and a vitamin B3.
WO2023094277A1 (en) 2021-11-26 2023-06-01 L'oreal Cosmetic water-in-oil emulsion comprising a specific water-soluble uv screening agent, a base, a volatile oil, a hydrophobic film-forming polymer, a polyoxyalkylenated linear polydimethylmethylsiloxane and a vitamin b3
WO2023118530A1 (en) 2021-12-23 2023-06-29 L'oreal Cosmetic composition comprising a polyhydroxyalkanoate copolymer bearing a(n) (un)saturated hydrocarbon-based chain and a silicone polymer
FR3131205A1 (en) 2021-12-23 2023-06-30 L'oreal Cosmetic composition comprising a polyhydroxyalkanoate copolymer with an (un)saturated hydrocarbon chain, and a silicone polymer
FR3134989A1 (en) 2022-04-28 2023-11-03 L'oreal Makeup process with the application of a composition comprising a polyphenol and a polyoxyalkylene compound, and a coloring material then application of an anhydrous composition
FR3134988A1 (en) 2022-04-28 2023-11-03 L'oreal Make-up process with the application of a composition comprising a polyphenol and a polyoxyalkylenated and/or polyglycerolated compound, and a coloring material then application of a composition in the form of an emulsion
WO2023208806A1 (en) 2022-04-28 2023-11-02 L'oreal Makeup process with the application of a composition comprising a polyphenol and a polyoxyalkylenated compound, and a dyestuff, followed by the application of an anhydrous or emulsified composition
WO2023208802A1 (en) 2022-04-28 2023-11-02 L'oreal Makeup processes using a polyphenol and at least one polyglycerol compound, and compositions for performing the process
FR3152122A3 (en) 2023-08-17 2025-02-21 L'oreal COMPOSITION IN THE FORM OF A WATER-IN-OIL EMULSION AND ASSOCIATED PROCESSES
FR3152982A1 (en) 2023-09-20 2025-03-21 L'oreal Solid composition in powder form comprising a film-forming polymer in the solid state.
FR3152981A1 (en) 2023-09-20 2025-03-21 L'oreal Process for preparing a cosmetic composition comprising a powdery phase and a film-forming polymer solubilized in a volatile solvent; pigment formulation.
WO2025061352A1 (en) 2023-09-20 2025-03-27 L'oreal Process for preparing a cosmetic composition comprising a pulverulent phase and a film-forming polymer solubilized in a volatile solvent; and pigment formulation.
WO2025061338A1 (en) 2023-09-20 2025-03-27 L'oreal Solid composition in powder form comprising a film-forming polymer in the solid state
FR3154006A1 (en) 2023-10-16 2025-04-18 L'oreal Low water W/O emulsion comprising a hydrophobic film-forming polymer, a linear silicone polyol, hyaluronic acid, vitamin B3 and a xanthic base
WO2025082655A1 (en) 2023-10-16 2025-04-24 L'oreal Low water content w/o emulsion comprising a hydrophobic film-forming polymer, a linear silicone polyol, hyaluronic acid, a vitamin b3 and a xanthine base
FR3154317A3 (en) 2023-10-18 2025-04-25 L'oreal EMULSION COMPOSITIONS CONTAINING A CARBOSILOXANE DENDRIMER COMPOUND AND A WATER-BASED FILM FORMER
FR3156036A1 (en) 2023-11-30 2025-06-06 L'oreal INVERT LIQUID EMULSION WITH A FILM-FORMING SILICONE POLYMER, OPTIONALLY A TITANIUM DIOXIDE-BASED PIGMENT AND BORON NITRIDE PARTICLES
WO2025132142A1 (en) 2023-12-20 2025-06-26 L'oreal Invert emulsion comprising pullulan, an apolar hydrocarbon-based oil, a silicone film-forming polymer and a dyestuff, and makeup process
FR3157183A1 (en) 2023-12-20 2025-06-27 L'oreal INVERSE EMULSION COMPRISING PULLULAN, AN APOLAR HYDROCARBON OIL, A SILICONE FILMLOGEN POLYMER, A COLORING MATERIAL AND MAKE-UP PROCESS
FR3158227A1 (en) 2024-01-17 2025-07-18 L'oreal Cosmetic water-in-oil emulsion comprising a volatile oil, a hydrophobic film-forming polymer, a polyoxyalkylenated linear polydimethylmethylsiloxane and a vitamin B3.
WO2025153358A1 (en) 2024-01-17 2025-07-24 L'oreal Cosmetic water-in-oil emulsion comprising a volatile oil, a hydrophobic film-forming polymer, a polyoxyalkylenated linear polydimethylmethylsiloxane and a vitamin b3
WO2026008482A1 (en) 2024-07-02 2026-01-08 L V M H Recherche Glossy, solid, anhydrous, transfer-free composition
WO2026008495A1 (en) 2024-07-02 2026-01-08 L V M H Recherche Glossy, transfer-resistant anhydrous composition
WO2026008483A1 (en) 2024-07-02 2026-01-08 L V M H Recherche Glossy anhydrous non-transfer liquid composition
FR3164121A1 (en) 2024-07-02 2026-01-09 L V M H Recherche Glossy, non-transfer anhydrous composition
FR3164119A1 (en) 2024-07-02 2026-01-09 L V M H Recherche Glossy, non-transferable, solid, anhydrous composition
FR3164120A1 (en) 2024-07-02 2026-01-09 L V M H Recherche Glossy, transfer-proof formula
FR3164118A1 (en) 2024-07-02 2026-01-09 L V M H Recherche Glossy, non-transferable, anhydrous liquid composition
WO2026082628A1 (en) 2024-10-18 2026-04-23 L'oreal Composition comprising a polyester and a lipophilic silicone polymer
FR3167545A1 (en) 2024-10-18 2026-04-24 L'oreal Composition comprising a polyester and a lipophilic silicone polymer

Also Published As

Publication number Publication date
JP2003226611A (en) 2003-08-12
JP4693330B2 (en) 2011-06-01
US7488492B2 (en) 2009-02-10
ATE373463T1 (en) 2007-10-15
EP1448154A2 (en) 2004-08-25
DE60222579T2 (en) 2008-06-12
AU2002361070A8 (en) 2003-06-10
AU2002361070A1 (en) 2003-06-10
WO2003045337A3 (en) 2004-02-19
EP1448154B1 (en) 2007-09-19
DE60222579D1 (en) 2007-10-31
US20050008597A1 (en) 2005-01-13

Similar Documents

Publication Publication Date Title
US7488492B2 (en) Cosmetic raw material cosmetic product and method for manufacturing a cosmetic product
JP4009382B2 (en) Cosmetic raw materials, cosmetics and methods for producing cosmetics
US6280748B1 (en) Cosmetic raw material cosmetic product and method for manufacturing cosmetic products
JP4229548B2 (en) Cosmetics and method for producing cosmetics
CN103079538B (en) Cosmetics for hair containing co-modified organopolysiloxane
KR102689624B1 (en) Film forming agents for cosmetics and cosmetics containing the same
CN104136002B (en) Personal care composition containing ionic organosilicon and film forming agent
JP5725709B2 (en) Acrylate-crosslinked silicone copolymer network.
EP2328949B1 (en) Silicone-organic hybrid emulsions in personal care applications
JP5669388B2 (en) Cosmetic composition utilizing a network of acrylate cross-linked silicone copolymers
CN104606075B (en) Copolymer resin powder, preparation method and cosmetics based on organosilicon
JPH10512233A (en) Polymers in cosmetics and body care products
KR20150047521A (en) Copolymer having carbosiloxane dendrimer structure and composition and cosmetic containing the same
CN108884226B (en) Composition comprising organosiloxane nanolatex and preparation of organosiloxane nanolatex
EP2231753A1 (en) Method of producing amino acid-modified organopolysiloxane emulsions
JP7257147B2 (en) Crosslinked polyorganosiloxane and personal care compositions containing same
JP4152534B2 (en) Cosmetics and method for producing the same
CN111902127A (en) Composition for caring for and/or making up keratin materials

Legal Events

Date Code Title Description
AK Designated states

Kind code of ref document: A2

Designated state(s): AE AG AL AM AT AU AZ BA BB BG BR BY BZ CA CH CN CO CR CU CZ DE DK DM DZ EC EE ES FI GB GD GE GH GM HR HU ID IL IN IS KE KG KP KR KZ LC LK LR LS LT LU LV MA MD MG MK MN MW MX MZ NO NZ OM PH PL PT RO RU SD SE SG SI SK SL TJ TM TN TR TT TZ UA UG US UZ VC VN YU ZA ZM ZW

AL Designated countries for regional patents

Kind code of ref document: A2

Designated state(s): GH GM KE LS MW MZ SD SL SZ TZ UG ZM ZW AM AZ BY KG KZ MD RU TJ TM AT BE BG CH CY CZ DE DK EE ES FI FR GB GR IE IT LU MC NL PT SE SK TR BF BJ CF CG CI CM GA GN GQ GW ML MR NE SN TD TG

121 Ep: the epo has been informed by wipo that ep was designated in this application
DFPE Request for preliminary examination filed prior to expiration of 19th month from priority date (pct application filed before 20040101)
WWE Wipo information: entry into national phase

Ref document number: 10496022

Country of ref document: US

WWE Wipo information: entry into national phase

Ref document number: 2002791950

Country of ref document: EP

WWP Wipo information: published in national office

Ref document number: 2002791950

Country of ref document: EP

WWG Wipo information: grant in national office

Ref document number: 2002791950

Country of ref document: EP