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WO2018186138A1 - Composition cosmétique, produit cosmétique et agent filmogène - Google Patents

Composition cosmétique, produit cosmétique et agent filmogène Download PDF

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Publication number
WO2018186138A1
WO2018186138A1 PCT/JP2018/010181 JP2018010181W WO2018186138A1 WO 2018186138 A1 WO2018186138 A1 WO 2018186138A1 JP 2018010181 W JP2018010181 W JP 2018010181W WO 2018186138 A1 WO2018186138 A1 WO 2018186138A1
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Prior art keywords
component
cosmetic
hair
weight
water
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Ceased
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PCT/JP2018/010181
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English (en)
Japanese (ja)
Inventor
常仁 杉浦
康枝 神崎
堀　誠司
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DuPont Toray Specialty Materials KK
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Dow Corning Toray Co Ltd
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    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F220/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride ester, amide, imide or nitrile thereof
    • C08F220/02—Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
    • C08F220/10—Esters
    • C08F220/34—Esters containing nitrogen, e.g. N,N-dimethylaminoethyl (meth)acrylate
    • C08F220/343—Esters containing nitrogen, e.g. N,N-dimethylaminoethyl (meth)acrylate in the form of urethane links
    • C08F220/346—Esters containing nitrogen, e.g. N,N-dimethylaminoethyl (meth)acrylate in the form of urethane links and further oxygen
    • 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
    • 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
    • A61K8/40—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing nitrogen
    • A61K8/41—Amines
    • 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
    • A61K8/84—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions otherwise than those involving only carbon-carbon unsaturated bonds
    • A61K8/89—Polysiloxanes
    • A61K8/895—Polysiloxanes containing silicon bound to unsaturated aliphatic groups, e.g. vinyl dimethicone
    • 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
    • A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q5/00—Preparations for care of the hair
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F2/00—Processes of polymerisation
    • C08F2/12—Polymerisation in non-solvents
    • C08F2/16—Aqueous medium
    • C08F2/22—Emulsion polymerisation
    • C08F2/24—Emulsion polymerisation with the aid of emulsifying agents
    • C08F2/28—Emulsion polymerisation with the aid of emulsifying agents cationic
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F230/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and containing phosphorus, selenium, tellurium or a metal
    • C08F230/04—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and containing phosphorus, selenium, tellurium or a metal containing a metal
    • C08F230/08—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and containing phosphorus, selenium, tellurium or a metal containing a metal containing silicon
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L33/00—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides or nitriles thereof; Compositions of derivatives of such polymers
    • C08L33/04—Homopolymers or copolymers of esters
    • C08L33/06—Homopolymers or copolymers of esters of esters containing only carbon, hydrogen and oxygen, which oxygen atoms are present only as part of the carboxyl radical
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L43/00—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and containing boron, silicon, phosphorus, selenium, tellurium or a metal; Compositions of derivatives of such polymers
    • C08L43/04—Homopolymers or copolymers of monomers containing silicon
    • D—TEXTILES; PAPER
    • D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M13/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
    • D06M13/322—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing nitrogen
    • D06M13/46—Compounds containing quaternary nitrogen atoms
    • D06M13/463—Compounds containing quaternary nitrogen atoms derived from monoamines
    • D—TEXTILES; PAPER
    • D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M15/00—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
    • D06M15/19—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
    • D06M15/21—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • D06M15/263—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds of unsaturated carboxylic acids; Salts or esters thereof

Definitions

  • the present invention relates to a film-forming agent, a cosmetic composition using the same, and a cosmetic having the same.
  • water-in-oil emulsions can generally impart physical properties that can enhance water resistance and durability, and thus have been used in a wide range of skincare products from sunscreen products.
  • a technology to form a coating film using a vinyl polymer having a carbosiloxane dendrimer structure in the side chain has been developed.
  • a cosmetic coating film can be formed, water resistance and sebum resistance.
  • makeup durability such as friction resistance.
  • oil-soluble film forming agents can be highly blended, water-in-oil skin cosmetics having a vinyl polymer having a carbosiloxane dendrimer structure in the side chain as an oil phase have been developed.
  • the present applicant uses an oil in emulsion particles by using a polymer emulsion obtained by emulsion polymerization of a vinyl monomer having a carbosiloxane dendrimer structure in the side chain in an aqueous phase. It has been found that a high molecular weight vinyl polymer can be formed in the phase, and a film forming agent using the vinyl polymer and a cosmetic composition using the same have been proposed (Patent Document 5). However, when the vinyl polymer obtained by the emulsion polymerization is applied to a cosmetic for hair use or as a film-forming agent for fibers including hair, the film-forming function or affinity with other components, etc. Left room for further improvement.
  • the present inventors use a polymer emulsion obtained by emulsion polymerization of a vinyl-based monomer having a carbosiloxane dendrimer structure in the side chain in an aqueous phase as a hair cosmetic or a film-forming agent for fibers including hair.
  • the above vinyl polymer has been found to have insufficient performance and affinity with other components.
  • cationic surfactants such as quaternary ammonium salts are widely used, but the above vinyl polymers and the like particularly leave room for improvement in affinity with cationic surfactants.
  • the film-forming property or the like cannot be sufficiently exhibited as compared with cosmetics using an anionic surfactant or the like.
  • the present invention has been made to solve the above-described problems, and even when used for cosmetics for hair or a film-forming agent for fibers including hair, excellent film-forming properties, feeling of use, and stability of blending. It is an object of the present invention to provide a cosmetic or film-forming agent using a vinyl polymer having a carbosiloxane dendrimer structure in the side chain, which can realize the properties.
  • component (A) at least one vinyl polymer having at least one carbosiloxane dendrimer structure in the side chain 100 parts by weight (B) cationic surfactant 0.1 to 30 parts by weight (X) water
  • a cosmetic composition or film-forming agent in which at least emulsified particles composed of component (A) and component (B) are in the aqueous phase, and the weight average molecular weight of component (A) is at least 80,000. Is achieved.
  • said component (A) is (A1) an unsaturated monomer having a carbosiloxane dendrimer structure having an organic group capable of radical polymerization; (A2) A monomer having a radical polymerizable vinyl group (B), which is different from the component (a1), and (Y) a cationic surfactant in the aqueous phase in the presence of a water-soluble azo radical initiator.
  • the vinyl polymer obtained by copolymerization is preferably used, and the above-described problems can be suitably solved.
  • the cosmetic composition or film forming agent of the present invention has a carbosiloxane dendrimer structure in an aqueous phase by an emulsion polymerization reaction using a cationic surfactant, preferably (Y) a water-soluble azo radical initiator. Since a vinyl polymer emulsion having a side chain is formed, a high molecular weight vinyl polymer can be formed in the oil phase in the emulsion particles, and it can be stably incorporated into a system containing a cationic surfactant. And there exists an advantage that a usability
  • the film-forming agent of the present invention and the cosmetic composition using the same are easy to design a polymer, have a feeling of use and a smooth finish, water resistance, sebum resistance, makeup durability, friction resistance, flexibility, Excellent uniformity and hair adhesion.
  • the blending amount of the carbosiloxane dendrimer can be easily adjusted, and the emulsion particle size can be finely adjusted, so that the stability of the emulsion is high.
  • the cosmetic composition or film-forming agent of the present invention comprises (A) at least one vinyl polymer having at least one carbosiloxane dendrimer structure in the side chain 100 parts by weight (B) a cationic surfactant 0.1 to 30 parts by weight Part (X) Water A composition comprising at least Here, the vinyl polymer as the component (A) is preferably a vinyl polymer obtained by an emulsion polymerization reaction using (B ′) a surfactant, and (B ′) one or more surfactants. It is preferable to be a cationic surfactant or a combination of a cationic surfactant and a nonionic surfactant.
  • the vinyl polymer as component (A) is subjected to an emulsion polymerization reaction in the presence of a cationic surfactant, it is particularly preferable to use (Y) a water-soluble azo radical initiator. Details will be described below.
  • the component (A) of the present invention has at least one vinyl polymer having a side chain having at least one carbosiloxane dendrimer structure (hereinafter sometimes referred to as “vinyl polymer”).
  • the component (a1) is a carbosiloxane dendrimer structure.
  • the component (a1) is preferably an unsaturated monomer having a carbosiloxane dendrimer structure represented by the formula (1).
  • L i + 1 represents a hydrogen atom, an alkyl group having 1 to 10 carbon atoms, an aryl group or an aralkyl group, and when i ⁇ c, the silylalkyl group And a i is an integer from 0 to 3) ⁇ .
  • the carbosiloxane dendrimer structure is a chemical structure highly branched radially from one silicon atom, and i indicating the total number of layers of the silylalkyl group indicates the degree of branching. For example, when the total number of layers i is 1 and L i + 1 is, for example, a methyl group, the carbosiloxane dendrimer structure means the following structure. (Wherein, Z, p, R 1 and R 2 are the same as above, and a 1 is an integer of 0 to 3)
  • said a, a 1 and a 2 are 0, and especially the following are preferable as said carbosiloxane dendrimer structure. (Wherein Z and R 2 are the same as above) (Wherein Z and R 2 are the same as above)
  • the unsaturation-containing group of the component (a1) is not limited as long as it has unsaturation capable of radical polymerization, and examples thereof include a vinyl group, an allyl group, and a (meth) acryl group.
  • the component (a1) is preferably an acrylic acid ester monomer or a methacrylic acid ester monomer having the above carbosiloxane dendrimer structure.
  • a particularly preferable unsaturated monomer is represented by the following structure.
  • the unsaturated monomer is an unsaturated monomer bonded to a silicon atom (Si) through — (Z) p— or —Z— in the carbosiloxane dendrimer structure described above.
  • R 4 is a hydrogen atom or a methyl group, and R 5 is an alkylene group having 1 to 10 carbon atoms), or (Wherein, R 4 and R 5 are the same as defined above), and an acrylic group or methacryl group-containing organic group.
  • the component (a2) constituting the component (A) is an unsaturated monomer different from the component (a1), and may be any monomer having a radical polymerizable vinyl group. Etc. are not particularly limited. More specifically, it is a vinyl monomer having no carbosiloxane dendrimer structure in the molecule.
  • vinyl monomers there are monomers that are starting materials of organic resins generally referred to as vinyl resins, specifically, methyl (meth) acrylate, (meth) acrylic acid.
  • Lower alkyl (meth) acrylates such as ethyl, n-propyl (meth) acrylate, isopropyl (meth) acrylate; glycidyl (meth) acrylate; n-butyl (meth) acrylate, isobutyl (meth) acrylate, ( Tert-butyl (meth) acrylate, n-hexyl (meth) acrylate, cyclohexyl (meth) acrylate, 2-ethylhexyl (meth) acrylate, octyl (meth) acrylate, lauryl (meth) acrylate, (meth) Higher (meth) acrylates such as stearyl acrylate; lower fatty acid vinyls such as vinyl acetate and
  • Aromatic vinyl monomers such as (meth) acrylamide, N-methylol (meth) acrylamide, N-methoxymethyl (meth) acrylamide, isobutoxymethoxy (meth) acrylamide, N, N-dimethyl (meth) acrylamide Group-containing vinyl monomers; hydroxyl group-containing vinyl monomers such as 2-hydroxyethyl (meth) acrylate, 2-hydroxybutyl (meth) acrylate, 2-hydroxypropyl (meth) acrylate: trifluoropropyl (meth) Fluorine-containing vinyl monomers such as acrylate, perfluorobutylethyl (meth) acrylate, and perfluorooctylethyl (meth) acrylate; epoxy groups such as glycidyl (meth) acrylate and 3,4 epoxycyclohexylmethyl (meth) acrylate Vinyl monomers; (meth) acrylic acid, itaconic acid, crotonic acid,
  • Ether type vinyl monomer (meth) acryloxypropyltrimethoxysilane, polydimethylsiloxane containing (meth) acrylic group at one end (branched or straight chain), styryl group at one end Unsaturated group-containing silicone compounds such as polydimethylsiloxane; butadiene; vinyl chloride; vinylidene chloride; (meth) acrylonitrile; dibutyl fumarate; maleic anhydride; dodecyl succinic anhydride; (meth) acryl glycidyl ether: (meta ) Radical polymerizable unsaturated carboxylic acid alkali metal salt, ammonium salt, organic amine salt such as acrylic acid, itaconic acid, crotonic acid, fumaric acid, maleic acid; radical polymerizable having sulfonic acid group such as styrene sulfonic acid Unsaturated monomers, and their alkali metal salts, ammo Um
  • Polyfunctional vinyl monomers can also be used.
  • trimethylolpropane tri (meth) acrylate, pentaerythritol tri (meth) acrylate, ethylene glycol di (meth) acrylate, tetraethylene glycol di (meth) acrylate Polyethylene glycol di (meth) acrylate, 1,4-butanediol di (meth) acrylate, 1,6-hexanediol di (meth) acrylate, neopentyl glycol di (meth) acrylate, trimethylolpropane trioxyethyl (meta ) Acrylate, tris (2-hydroxyethyl) isocyanurate di (meth) acrylate, tris (2-hydroxyethyl) isocyanurate tri (meth) acrylate, ethylene oxide of bisphenol A or Di (meth) acrylates of diols of adducts of lopyrene oxides, di (meth)
  • an organic silicon compound having a vinyl radical polymerizable unsaturated group and a hydrolyzable group can also be used.
  • the radical polymerizable group include (meth) acryloxy group-containing organic groups, (meth) acrylamide group-containing organic groups, styryl group-containing organic groups, alkenyl groups having 2 to 10 carbon atoms, vinyloxy groups, and aryloxy groups. Is mentioned.
  • the component (a1) is preferably 45% to 60% by weight based on the total monomer units.
  • the method for producing a cosmetic composition used in the present invention includes the following components (A) and (B): (A) (a1) an unsaturated monomer having a carbosiloxane dendrimer structure having an organic group capable of radical polymerization; (A2) A monomer having a radically polymerizable vinyl group (B ′) different from the component (a1) (B ′) A surfactant containing a cationic surfactant (where component (B) is component (A) 100)
  • the range satisfying the relationship of 0.1 to 30 parts by weight with respect to parts by weight) is obtained by copolymerization in the aqueous phase.
  • the weight ratio of component (A) to component (B ′) is preferably 0.1 to 10 parts by weight with respect to 100 parts by weight of component (A). .
  • JP-A-11-1530 JP-A-2000-63225, JP-A-2001-192424, JP-A-2014-40512, etc. Can be produced according to the production method described in 1. above.
  • Component (B ′) is a surfactant used for emulsion polymerization of the vinyl polymer as component (A), and is an ionic surfactant (anionic surfactant, cationic surfactant, amphoteric surfactant, Polar surfactants) and nonionic surfactants containing a cationic surfactant are used.
  • ionic surfactant anionic surfactant, cationic surfactant, amphoteric surfactant, Polar surfactants
  • nonionic surfactants containing a cationic surfactant are used.
  • One type of surfactant or a combination of two or more types can also be used.
  • the reactive surfactant which has a radical polymerization group can also be used for this component (B ').
  • the component (B ′) when an anionic surfactant or the like is used as the component (B ′), the blending stability and film-forming property in the system containing the cationic surfactant that is the object of the present invention may be impaired.
  • the component (B ′) preferably contains a cationic surfactant and does not contain other ionic surfactants.
  • the cationic surfactant or the cationic surfactant and the nonionic surfactant Combinations are particularly preferred. These surfactants are the same as those exemplified later, but it is particularly preferable that a cationic surfactant of a quaternary ammonium salt be included. Specific types of these surfactants will be described later.
  • the component (A) of the present invention 0.01 to 20 parts by weight of a radical polymerization initiator is added to 100 parts by weight of the mixture of the component (a1) and the component (a2), and the component (B ′) It is obtained by preparing an emulsified dispersion (cosmetic composition) in an aqueous medium containing water and subjecting it to emulsion polymerization (copolymerization) to give a water-dispersed vinyl copolymer.
  • the emulsion particles of the vinyl copolymer thus obtained have a structure having a hydrophilic group on the outer periphery thereof. Therefore, even in oil-in-water cosmetics and water-in-oil cosmetics, the emulsion particles of the vinyl copolymer should be blended on the water phase side. Is possible.
  • the component (a1), the component (a2) and the radical polymerization initiator may be emulsified and dispersed together, or the radical polymerization initiator may be added after emulsifying and dispersing in advance.
  • the radical polymerization initiator is not particularly limited as long as it is a radical polymerization initiator usually used for emulsion polymerization of vinyl polymers.
  • inorganic peroxides such as potassium persulfate, sodium persulfate, and ammonium persulfate
  • water-soluble peroxides such as organic peroxides such as t-butyl peroxymaleic acid, succinic acid peroxide, and t-butyl hydroperoxide.
  • the component (A) of the present invention is preferably subjected to an emulsion polymerization reaction with a cationic surfactant or a combination of a cationic surfactant and a nonionic surfactant.
  • the radical polymerization initiator is preferably (Y) a water-soluble azo radical initiator, and the vinyl polymer in which the weight average molecular weight of the component (A) is at least 80,000 without inhibiting the polymerization reaction. Can be easily synthesized.
  • the component (Y) may be entirely consumed by the emulsion polymerization reaction, and a small amount of the unreacted component (Y) in the emulsified particles or the aqueous phase of the component (A) constituting the cosmetic or film-forming agent. May remain.
  • a cosmetic or film-forming agent is included in a preferred embodiment of the present invention as having one of the compositional characteristics of component (A) emulsion-polymerized using component (Y).
  • the blending amount of the radical polymerization initiator is in the range of 0.01 to 20 parts by weight, and in the range of 0.1 to 10 parts by weight with respect to the total of 100 parts by weight of the component (a1) and the component (a2). It is preferable that
  • the emulsified dispersion is prepared using a normal emulsifying apparatus such as a colloid mill or a homogenizer.
  • the polymerization is performed for about 2 to 12 hours by heating the reaction system to 50 to 90 ° C. in advance. At this time, polymerization may be performed while dropping the emulsified dispersion, or polymerization may be performed after the emulsified dispersion is charged all at once.
  • the weight average molecular weight of the vinyl polymer having a carbosiloxane dendrimer structure as the component (A) used in the present invention is at least 80,000 or more from the viewpoint of the strength and performance of the film forming agent and ease of blending. More preferably, they are 160,000 or more, 240,000 or more, More preferably, it is 500,000 or more. Further, the upper limit of the weight average molecular weight may be 80,000,000 or less, preferably 40,000,000 or less, more preferably 10,000,000 or 8,000,000 or less.
  • the property may be any of liquid, gum, paste, solid, etc. at room temperature, but is preferably solid from the viewpoint of the durability of the resulting cosmetic film. From the viewpoint of compoundability, it is preferable to use a solution or dispersion diluted with a solvent.
  • component (A) can be used, and it is contained in the total composition in an amount of 0.1 to 15% by weight, preferably 0.5 to 10% by weight.
  • the blending amount of component (A) is less than the lower limit, film-forming properties on keratin such as hair, persistence and feel may be insufficient, When the upper limit is exceeded, the film feeling becomes too strong, and the touch such as fingering may be deteriorated.
  • a surfactant is used according to its application.
  • a surfactant used for emulsification in a cosmetic component (B) a cationic surfactant, and optionally (B1) a nonionic surfactant can be mainly used.
  • other ionic surfactants anionic surfactants, amphoteric surfactants, semipolar surfactants
  • polymer emulsifiers may be blended.
  • anionic surfactants anionic surfactants, amphoteric surfactants, semipolar surfactants
  • the cationic surfactant is an essential component of the cosmetic composition or film-forming agent of the present invention, and may be an emulsifier of a monomer component in the emulsion polymerization described above. It may be a detergent component. Particularly, in the case of a film forming agent for use in hair cosmetics and fiber treatment agents, a cationic surfactant is often used.
  • the component (A) of the present invention is preferably a cationic surfactant. It is obtained by an emulsion polymerization reaction in the presence of an agent, and has a feature that its feeling of use, blending stability and film-forming property are not impaired.
  • Such component (B) is preferably a cationic surfactant of a quaternary ammonium salt, and is represented by the general formula [R 1 4 N] + .X ⁇ (wherein at least one of the four R 1 is Represents an alkyl group having 8 to 28 carbon atoms, an alkenyl group having 8 to 28 carbon atoms, or an acrylamide-containing group having 8 to 28 carbon atoms, the remainder being a benzyl group or an alkyl group having 1 to 5 carbon atoms; Is preferably a halogen ion or an organic anion).
  • X- is preferably a chloride ion (Cl ⁇ ) or a bromide ion (Br ⁇ ), but is not limited thereto.
  • cationic surfactant as component (B) include alkyltrimethylammonium chloride, stearyltrimethylammonium chloride, lauryltrimethylammonium chloride, cetyltrimethylammonium chloride, tallow alkyltrimethylammonium chloride, behenyltrimethylammonium chloride, bromide.
  • Stearyltrimethylammonium behenyltrimethylammonium bromide, distearyldimethylammonium chloride, dicocoyldimethylammonium chloride, dioctyldimethylammonium chloride, di (POE) oleylmethylammonium chloride (2EO), benzalkonium chloride, alkylbenzalkonium chloride, Alkyldimethylbenzalkonium chloride, benzethonium chloride, stearyldimethylbenzylammonium chloride, Norin-derived quaternary ammonium salt, diethylaminoethylamide stearate, dimethylaminopropylamide stearate, amidopropyldimethylhydroxypropylammonium chloride, stearoylcholaminoformylmethylpyridinium chloride, cetylpyridinium chloride, tall oil alkylbenzylhydroxyethylimidazo Examples include linium and benzyl
  • the cosmetic composition of the present invention preferably further contains (B1) a nonionic surfactant.
  • nonionic surfactants include polyoxyalkylene ethers, polyoxyalkylene alkyl ethers, polyoxyalkylene fatty acid esters, polyoxyalkylene fatty acid diesters, polyoxyalkylene resin acid esters, polyoxyalkylene (cured) Castor oils, polyoxyalkylene alkyl phenols, polyoxyalkylene alkyl phenyl ethers, polyoxyalkylene phenyl phenyl ethers, polyoxyalkylene alkyl esters, polyoxyalkylene alkyl esters, sorbitan fatty acid esters, polyoxyalkylene sorbitan alkyl esters , Polyoxyalkylene sorbitan fatty acid esters, polyoxyalkylene sorbit fatty acid esters, polyoxyalkyl N-glycerin fatty acid esters, polyglycerin alkyl ethers, polyglycerin
  • polyoxyalkylene-modified silicone, polyglyceryl-modified silicone, glyceryl-modified silicone, and sugar alcohol-modified silicone are preferably those in which alkyl branch, linear silicone branch, siloxane dendrimer branch, etc. are applied at the same time as the hydrophilic group.
  • alkyl branch, linear silicone branch, siloxane dendrimer branch, etc. are applied at the same time as the hydrophilic group.
  • polyglyceryl-based nonionic surfactants such as polyglyceryl monolaurate (polyglyceryl-6 laurate, polyglyceryl-10 laurate), polyglyceryl monostearate (polyglyceryl-10 stearate) are selected. You may do it.
  • the cationic surfactant as component (B) is a quaternary ammonium salt derived from methacrylic acid, from the viewpoint of emulsion polymerization reactivity, (B1-1) reactive nonionic surfactant It is particularly preferable to use in combination.
  • the reactive nonionic surfactant has a radical polymerization group such as an alkenyl group or a (meth) acryl group having a linear or branched structure, and the hydrophilic group is made of ethylene oxide, propylene oxide or butylene oxide. However, only ethylene oxide may be used, or ethylene oxide and propylene oxide or butylene oxide may be used in combination.
  • the cloud point is preferably 50 ° C or higher, more preferably 70 ° C or higher, and further 80 ° C or higher. preferable. If the cloud point is less than 50 ° C., the emulsifying ability of the nonionic surfactant is impaired, and a problem may occur in the stability of the emulsion obtained by emulsifying the monomer during radical polymerization, and a uniform emulsion may not be obtained.
  • amphoteric surfactants include N-acylamidopropyl-N, N-dimethylammoniobetaines, N-acylamidopropyl-N, N'-dimethyl-N'- ⁇ -hydroxypropylammonio
  • Imidazoline-type amphoteric surfactants alkylbetaine-type amphoteric surfactants such as lauryldimethylaminoacetic acid betaine and myristylbetaine; palm oil fatty acid amidopropyldimethylaminoacetic acid betaine, palm kernel fatty acid amidopropyldimethylaminoacetic acid betaine, beef tallow fatty acid amidopropyl Dimethylaminoacetic acid betaine, hardened beef tallow fatty acid amidopropyl dimethylaminoacetic acid betaine, lauric acid amidopropyl dimethylaminoacetic acid betaine, myristic acid amidopropyl dimethylaminoacetic acid betaine, palmitic acid amido Amidobetaine amphoteric surfactants such as pyrdimethylaminoacetic acid betaine, amidopropyl stearate dimethylaminoacetic acid betaine, oleic acid amidopropyldimethylamino
  • the semipolar surfactant examples include alkylamine oxide type surfactants, alkylamine oxides, alkylamidoamine oxides, alkylhydroxyamine oxides, and the like.
  • Alkoxyethyldihydroxyethylamine oxide and the like are preferably used.
  • the amount of the component (B) surfactant used is preferably 0.1 to 30 parts by weight, more preferably 0.1 to 10 parts by weight with respect to 100 parts by weight of the component (A). If it exceeds 30 parts by weight, the performance of the component (A) may be insufficient. On the other hand, if the amount is less than 0.1 part by weight, the component (A) cannot be stably emulsified.
  • the blending amount thereof is preferably 0.1 to 30 parts by weight with respect to 100 parts by weight of the component (A). More preferably, it is 0.1 to 10 parts by weight. If it exceeds 30 parts by weight, the performance of the component (A) may be insufficient. On the other hand, if the amount is less than 0.1 part by weight, the component (A) cannot be stably emulsified.
  • a part of polymer emulsifier overlaps the function and kind of (c2) hydrophilic thickener mentioned later.
  • the weight average molecular weight of the polymer emulsifier used is preferably 40,000 to 3,000,000, more preferably 300,000 to 2,750,000, and more preferably 2,000,000 to 2,500,000.
  • an anionic polymer for example, as stearoxy PG hydroxyethyl cellulose sulfonate Na (INCI: SODIUM STEARROXY PG-HYDROXYETHYLCELLULOSE SULFONATE) (Poise 310 (Kao Corporation)), etc.
  • commercially available products such as carrageenan and locust bean gum.
  • alkyl acrylate, alkyl methacrylate, polyoxyethylene (20) stearyl ether copolymer (INCI: ACRYLATES / STEARTH-20 METHACRYLATE COPOLYMER), alkyl acrylate / methacrylic acid Alkyl acid polyoxyethylene (25) lauryl ether copolymer (INCI: ACRYLATES / LAURETH-25 METHACRYLATE COPOLYMER), alkyl acrylate, alkyl methacrylate, polyoxyethylene (25) behenyl ether copolymer (INCI: ACRYLATES / BEHENETH-25 METHACRYLATE COPOLYMER), acrylic acid / methacrylic acid RUKYL copolymer (INCI: ACRYLATES / C10-30, ALKYL, ACRYLATE CROSSPOLYMER), acrylic acid / neodecanoic acid vinyl copolymer (INCI:
  • polymers include Aculine 88, Aculin 22, Aculin 28, Aculin 38 (above, Dow Chemical Japan), Carbopol ETD2020, Carbopol Ultrez 21, Carbopol Ultrez 20, PEMULEN TR-1, PEMULEN TR- Commercially available products such as 2 (above, Lubrizol Advanced Materials), STRUCTURE 2001, STRUCTURE XL, and STRUCTURE CEL (Akzo Nobel) can be used. *
  • nonionic polymers examples include hydroxyethyl cellulose, hydroxypropyl methylcellulose, hydroxypropyl guar gum, polyvinyl pyrrolidone, polyethylene glycol and the like. These weight average molecular weights are preferably 40,000 to 3,000,000, more preferably 300,000 to 2,750,000, and even more preferably 2,000,000 to 2,500,000.
  • Alcox series (Meisei Chemical Industry Co., Ltd., polyethylene glycol): Alcox E30 (weight average molecular weight 300,000 to 500,000), Alcox E-45 (weight average molecular weight 600,000 to 800,000) ), Alcox E-60 (weight average molecular weight 1 million to 1.2 million), Alcox E-75 (weight average molecular weight 2 million to 2.5 million), Alcox E-100 (weight average molecular weight 2.5 million to 3 million); Metrows series (Shin-Etsu Chemical Co., Ltd., hydroxypropyl methylcellulose): Metrows 60SH-10000 (weight average molecular weight 380,000); Jaguar HP series (Rhodia, hydroxypropyl guar gum), Jaguar HP8, HP105, HP-120 (all weight) Use a commercial product with an average molecular weight of 2,200,000) It can be. *
  • amphoteric polymers examples include copolymers of dimethyldiallylammonium chloride, acrylic acid and acrylamide (trade names: Marquat Plus 3330, 3331; manufactured by Nihon Lubrizol).
  • the component (A) is preferably emulsified using the component (B), and optionally further the component (B1), so that at least the component (A).
  • the volume average particle diameter (measured by a laser diffraction scattering method or the like) of the component (A) after emulsification in this cosmetic composition is preferably 500 nm or less, and more preferably 300 nm or less.
  • the component (A) is emulsified with the component (B) it becomes 50% by weight or more, preferably 70% by weight or more of the oil phase in the emulsified particles.
  • the obtained cosmetic composition can be used as a cosmetic raw material composition, an oil-in-water cosmetic composition, and a water-in-oil cosmetic composition. Furthermore, although it can be used as a raw material composition of a cosmetic together with other components, the oil-in-water cosmetic exhibits the characteristics as the cosmetic composition of the present invention.
  • Component (X) is water and is not particularly limited as long as it is generally used in cosmetics, quasi drugs, and pharmaceuticals.
  • purified water such as distilled water or ion exchange water, physiological saline, phosphate buffered aqueous solution, or the like can be used.
  • the content of the component (X) in the composition in the cosmetic composition is at least 50 parts, 70 parts, or 100 parts, more preferably 100 parts by weight of the component (A) from the viewpoint of emulsion formation. 200 parts are preferable.
  • the upper limit for the same reason, it is 2000 parts, 1500 parts, or 1200 parts, preferably 1000 parts, and more preferably 900 parts.
  • composition of the present invention containing a film forming agent is preferably used as a cosmetic composition, and is preferably used in a cosmetic using them. Moreover, in cosmetics, it can be used as skin cosmetics and / or hair cosmetics. In particular, it is suitable for use as a hair cosmetic or skin cosmetic comprising the above cosmetic composition and component (C) a cosmetically acceptable medium.
  • the component (C) cosmetically acceptable medium used in the present invention includes the following components (c0) to (c4) or not limited to these, volatile or non-volatile, carbon-based, hydrocarbon-based, Fluoro and / or silicone oils and / or solvents of mineral, animal, vegetable or synthetic origin; fatty substances which are solid at room temperature, in particular waxes, pasty fatty substances and gums; water; hydrophilic organic solvents Dyes; polymers; vitamins, thickeners, gelling agents, trace elements, softeners, sequestering agents, fragrances, acidifying or basifying agents, preservatives, sunscreen agents, surfactants, antioxidants There are those containing at least one component selected from agents, hair removal inhibitors, antidandruff agents, sprays, ceramides, film-forming aids, or mixtures thereof.
  • the cosmetic composition of the present invention uses a cationic surfactant as a surfactant, from the viewpoint of stability at the time of emulsion, a cationic surfactant or cation used for a hair cosmetic or a fiber treatment agent is used. Excellent compatibility with functional polymers and blending stability. Therefore, it is desirable to mix the cosmetic composition of the present invention in a cosmetic or film-forming agent dosage form containing a cationic surfactant or cationic polymers.
  • Component (c0) used in the present invention is an alcohol, and includes a lower alcohol and a higher alcohol.
  • aliphatic alcohols and polyhydric alcohols having 1 to 9 carbon atoms can be preferably used.
  • the higher alcohol is, for example, a higher alcohol having 10 to 30 carbon atoms.
  • the higher alcohol is a saturated or unsaturated monohydric aliphatic alcohol, and the hydrocarbon group portion may be either linear or branched, but is more preferably linear. preferable.
  • Examples of the higher alcohol having 10 to 30 carbon atoms include lauryl alcohol, myristyl alcohol, palmityl alcohol, stearyl alcohol, behenyl alcohol, hexadecyl alcohol, oleyl alcohol, isostearyl alcohol, hexyldodecanol, octyldodecanol, cetostearyl.
  • Examples include alcohol, 2-decyltetradecinol, cholesterol, sitosterol, phytosterol, lanosterol, lanolin alcohol, hydrogenated lanolin alcohol, and the like.
  • a higher alcohol having a melting point of 40 to 80 ° C. alone, or to combine a plurality of higher alcohols so that the melting point is 40 to 70 ° C.
  • Such higher alcohols are particularly useful as a base for hair cosmetics because they form an aggregate called ⁇ -gel together with a surfactant to increase the viscosity of the preparation and stabilize the emulsion. is there.
  • the component (c1) used in the present invention includes an oil-soluble ultraviolet absorber and a water-soluble ultraviolet absorber.
  • oil-soluble ultraviolet absorbers include 2-methoxyhexyl paramethoxycinnamate (Ubinal MC80; manufactured by BASF), 2,4,6 tris [4- (2-ethylhexyloxycarbonyl) anilino] -1,3, 5-triazine (Ubinal T150; manufactured by BASF), 4-tert-butyl-4′-methoxydibenzoylmethane (parasol 1789; manufactured by DSM Nutrition Japan), octocrylene (parasol 340; manufactured by DSM Nutrition Japan), dimethoxybenzylidene dioxoimidazolidinepropionic acid 2-ethylhexyl (soft shade DH; manufactured by Ajinomoto Co.), diethylaminohydroxybenzoyl benzoic acid hexyl ester (ubibinal plus;
  • the water-soluble ultraviolet absorber examples include phenylbenzimidazole sulfonic acid, 3,4,5-trimethoxycinnamic acid N-2- (2-hydroxyethoxy) ethylamino, 4-methoxycinnamic acid N-2- (2- Hydroxyethoxy) ethylamide, sodium 2-hydroxy-4-methoxy-5-sulfoxonium benzophenone. It is preferable from the viewpoint of the ultraviolet absorption effect that one or more of such ultraviolet absorbers are combined.
  • the content of the ultraviolet absorber is in the range of 0.1 to 30% by weight in the total composition of the cosmetic, preferably in the range of 0.5 to 25% by weight, and further 1 to 20% by weight. The range of is good.
  • the stability is further improved by further blending the component (c2) hydrophilic thickener in addition to the essential components (A) and (B) in the composition.
  • the hydrophilic thickener used in the present invention is not particularly limited as long as it is used in cosmetics.
  • natural water-soluble polymer semi-synthetic water-soluble polymer, synthetic water-soluble polymer And inorganic water-soluble polymers.
  • the hydrophilic thickener may be a cationic water-soluble polymer such as cationized guar gum, and in the cosmetic composition of the present invention, it is particularly excellent in blending stability and conditioning effect, and is suitable for foaming and foaming.
  • it is excellent in touch, excellent in washing characteristics, and can provide smooth finger-feeling without squeaky feeling when wet after hair washing and when dry.
  • Some of these components may overlap in function and type with the polymer emulsifier.
  • examples of natural water-soluble polymers include gum arabic, gum tragacanth, galactan, guar gum, carob gum, caraya gum, carrageenan, pectin, agar, quince seed (malmello), algae colloid (gypsum extract), starch (rice, Corn, potato, wheat), plant polymers such as glycyrrhizic acid; microbial polymers such as xanthan gum, dextran, succinoglucan, and bullulan; animal polymers such as collagen, casein, albumin, and gelatin.
  • semi-synthetic water-soluble polymers include starch polymers such as carboxymethyl starch and methylhydroxypropyl starch; methylcellulose, nitrocellulose, ethylcellulose, methylhydroxypropylcellulose, hydroxyethylcellulose, sodium cellulose sulfate, hydroxypropylcellulose, carboxy Cellulose polymers such as sodium methylcellulose (CMC), crystalline cellulose and cellulose powder; and alginic acid polymers such as sodium alginate and propylene glycol alginate.
  • starch polymers such as carboxymethyl starch and methylhydroxypropyl starch
  • Cellulose polymers such as sodium methylcellulose (CMC), crystalline cellulose and cellulose powder
  • alginic acid polymers such as sodium alginate and propylene glycol alginate.
  • Examples of synthetic water-soluble polymers include vinyl polymers such as polyvinyl alcohol, polyvinyl methyl ether, polyvinyl pyrrolidone, and carboxyvinyl polymer (carbomer); polyoxyethylene polymers such as polyethylene glycol (molecular weights 1500, 4000, and 6000). Molecule: Polyoxyethylene polyoxypropylene copolymer copolymer polymer; sodium polyacrylate, polyethyl acrylate, polyacrylamide, acrylic acid / alkyl methacrylate copolymer (trade name “Pemulene TR-1”), etc. Acrylic polymer; polyethyleneimine, cationic polymer and the like.
  • Examples of the inorganic water-soluble polymer include bentonite, AlMg silicate (trade name “Begum”), laponite, hectorite, and silicic anhydride.
  • the acrylic polymer may be a homopolymer having a monomer selected from methacrylic acid, acrylic acid, methacrylate, acrylate, methacrylamide, and acrylamide, or a copolymer containing two or more of these monomers.
  • Carboxyvinyl polymer (Syntalene K, L; Wako Pure Chemical Industries, Ltd.), alkyl-modified carboxyvinyl polymer (PEMULEN TR-1, TR-2; Lubrizol), polyacrylamide (SEPIGL 305) sold by SEPPIC, (Nacryacrylate / acryloyldimethyltaurine Na) copolymer (SIMULGEL EG), (Hydroxyethyl acrylate / acryloyldimethyltaurine Na) copolymer (SIMULGEL FL, SI ULGEL NS, SEPIPLUS S, SEPINOV EMT 10), (acrylamide / ammonium acrylate) copolymer (SEPIPLUS 265), polyacrylates over 13 (SEPIPLUS 400), and the like.
  • One or more acrylic acid polymers selected from these can be used.
  • the preparation is stable even in a small amount, and the anti-shrinking effect at the time of application, It is preferable from the viewpoint of improving the feeling of use.
  • cationic water-soluble polymer examples include quaternary nitrogen-modified polysaccharides (for example, cation-modified cellulose, cation-modified hydroxyethyl cellulose, cation-modified guar gum, cation-modified locust bean gum, cation-modified starch), dimethyl chloride.
  • quaternary nitrogen-modified polysaccharides for example, cation-modified cellulose, cation-modified hydroxyethyl cellulose, cation-modified guar gum, cation-modified locust bean gum, cation-modified starch
  • dimethyl chloride for example, quaternary nitrogen-modified polysaccharides (for example, cation-modified cellulose, cation-modified hydroxyethyl cellulose, cation-modified guar gum, cation-modified locust bean gum, cation-modified starch), dimethyl chloride.
  • Diallylammonium derivatives for example, dimethyldiallylammonium chloride / acrylamide copolymer, polydimethylmethylenepiperidinium chloride, etc.
  • vinylpyrrolidone derivatives for example, vinylpyrrolidone / dimethylaminoethyl methacrylate copolymer salt, vinylpyrrolidone / methacrylamide
  • Propyltrimethylammonium chloride copolymer vinylpyrrolidone / methylvinylimidazolium chloride copolymer, etc.
  • methacrylic acid derivatives eg, methacryloyl ethyl
  • the blending amount of the hydrophilic thickener in the cosmetic of the present invention is preferably 0.1 to 5% by weight, more preferably 0.3 to 1.5% by weight, and still more preferably in the total composition of the cosmetic. Is 0.5 to 1% by weight. If the blending amount is less than 0.1% by weight, the stabilizing effect due to the addition may not be obtained. If the blending amount exceeds 5% by weight, it may become sticky or feel heavy during application.
  • the component (c3) inorganic powder used in the present invention includes pigments and UV protection agents.
  • pigments include colored pigments and extender pigments.
  • colored pigments include pigment grade titanium oxide, zinc oxide, aluminum oxide, barium sulfate, calcium carbonate, iron oxide, and carbon black.
  • extender pigments include talc, mica, and sericite.
  • the particle size is not particularly limited, but is preferably smaller than the emulsion particles in the cosmetic.
  • the ultraviolet protective agent has a particle size of less than 0.3 ⁇ m, and includes hydrophobized zinc oxide and / or hydrophobized titanium oxide.
  • the particle diameter is a volume-based average particle diameter measured using a laser diffraction particle size distribution analyzer using an organic solvent such as ethanol as a solvent. These are used to add shades to the cosmetics themselves or to reflect ultraviolet light.
  • component (c3) can be used, and it is contained in an amount of 0.1 to 25% by weight, preferably 2.0 to 10% by weight, based on the total composition of the cosmetic. If it is less than 0.1% by weight, the finish is not smooth, and if it exceeds 30% by weight, the feeling of use becomes worse.
  • the cosmetic of the present invention can contain powders used in ordinary cosmetics, and have a spherical shape, a plate shape, a needle shape, or the like;
  • the particle structure such as porous or nonporous can be used without particular limitation.
  • powders that are hydrophobic themselves include nylon powder, polymethyl methacrylate, acrylonitrile-methacrylic acid copolymer powder, vinylidene chloride-methacrylic acid copolymer powder, polyethylene powder, polystyrene powder, and organopolysiloxane.
  • powders that are not hydrophobic include, for example, titanium oxide, koji, ultramarine blue, red rose, yellow iron oxide, black iron oxide, zinc oxide, aluminum oxide, silicon dioxide, magnesium oxide, zirconium oxide, magnesium carbonate, and calcium carbonate.
  • a known hydrophobizing agent and a known hydrophobizing method may be used.
  • the surface treatment agent include fluorine compounds such as perfluoroalkyl phosphate ester and perfluoroalkylalkoxysilane, methyl hydrogen polysiloxane, cyclic silicone, one- or both-end trialkoxy group-modified organopolysiloxane, and the like.
  • fluorine compounds such as perfluoroalkyl phosphate ester and perfluoroalkylalkoxysilane, methyl hydrogen polysiloxane, cyclic silicone, one- or both-end trialkoxy group-modified organopolysiloxane, and the like.
  • silicone compounds include silicone compounds, metal soaps such as aluminum stearate and zinc stearate, and amino acid compounds such as lauroyllysine.
  • any silane-based treating agent may be used as long as it reacts with the inorganic fine powder to hydrophobize the surface thereof.
  • the surface of the inorganic fine powder is trimethylsilyl group, dimethylsilyl group
  • silane-based treatment agent capable of imparting a trimethylsilyl group examples include trimethylchlorosilane and hexamethyldisilane
  • examples of the silane-based treatment agent capable of imparting a dimethylsilyl group include dimethyldichlorosilane, dimethyldimethoxysilane, and polydimethylsilazane.
  • examples of the silane-based treatment agent that can impart a monomethylsilyl group include methyltrichlorosilane, methyltrimethoxysilane, octylsilane, and perfluoroalkylsilane.
  • ⁇ - (2-aminoethyl) aminopropyltrimethoxysilane ⁇ -methacryloxypropyltrimethoxysilane, ⁇ -glycidoxypropyltrimethoxysilane, vinyltriacetoxysilane, ⁇ -mercaptopropylmethyldimethoxysilane
  • a silane coupling agent having an organic functional group such as can be used.
  • methylhydrogenpolysiloxane treatment silicone resin treatment, silicone gum treatment, acrylic silicone treatment, organosiloxane treatment such as fluorinated silicone treatment, metal soap treatment such as zinc stearate treatment, perfluoro Fluorine compound treatment such as alkyl phosphate ester salt, perfluoropolyether treatment, amino acid treatment such as N-lauroyl-L-lysine treatment, oil agent treatment such as squalane treatment, acrylic treatment such as alkyl acrylate treatment, etc.
  • the surface treatment amount is not limited, but is preferably 0.5 to 20% by weight, more preferably 2 to 8% by weight based on the original powder.
  • the polyether-modified silicone of the optional component (c4) that can be used in the present invention may partially overlap with the nonionic surfactant according to the function in the cosmetic or cosmetic composition.
  • dimethylpolysiloxane is bonded with a polyoxyalkylene group, preferably a polyoxyethylene group or poly (oxyethylene oxypropylene), and has various bonding positions, HLB, and viscosity.
  • bonding position the side chain, one end, and both ends of the silicone chain are known.
  • a silicone chain and a polyoxyalkylene chain are bonded to the main chain in a block form. In the present invention, any bond position is used, but a side chain type or block type is preferred.
  • the HLB value of the polyether-modified silicone is defined by the Griffin method, and when used for a W / O-based cosmetic, a value of 1 to 6, particularly 2 to 5 is preferable. Further, when used for O / W cosmetics, those having a relatively high HLB of 7 to 13 are preferred.
  • the viscosity is preferably 20 to 100,000 mm2 / s at 25 ° C., more preferably 50 to 50,000 mm2 / s. Here, the viscosity was measured with a B-type viscometer.
  • the viscosity value (mPa ⁇ s) measured for 1 minute under the condition of 3 rotors and 12 rpm (1,000 mm2 / s or more and less than 10,000 mm2 / s) is directly read as kinematic viscosity (mm2 / s).
  • component (c4) polyether-modified silicone examples include SH-3771M (HLB13, viscosity 300 mm2 / s, Toray Dow Corning), SH-3775M (HLB5, viscosity 1600 mm2 / s, Toray Dow Corning) FZ-2233 (HLB3, viscosity 5000 mm2 / s, Toray Dow Corning), ES-5612 ⁇ Formation Aid (HLB4, viscosity 1000 mm2 / s, Toray Dow Corning), ES-5300 Formation Aid (HLB3, viscosity 1900 mm2 / s) s, Toray Dow Corning), ES-5600 Silicon Glycerol Emulsifier (HLB2, viscosity 3000mm2 / s, Toray Dow Corning), BY25-339 (HLB8) 5.
  • One or more of these polyether-modified silicones can be used, and are contained in the total composition in an amount of 0.1 to 6% by weight, preferably 0.3 to 2.4% by weight.
  • polar oil is liquid at 25 ° C.
  • the liquid state has fluidity, and includes a cream form and a paste form.
  • the polar oil is not particularly limited as long as it is used in ordinary cosmetics, but those having a solubility parameter (SP value) of 19 or more, particularly 19 to 23 are preferable.
  • nonpolar oil those having a solubility parameter (SP value) of less than 19, particularly 12 to 16, are preferable.
  • the SP value can be obtained by various methods. In the present invention, according to the method of Fedors (“POLYMER HANDBOOK 4th” by J. BRANDRUP, JHON WILEY & SONS, INC, issued in 1999), parameters shown in VII 685 to 686 are used. It is obtained by using.
  • Oils are one of the base materials for hair cosmetics, and in addition to the above higher alcohols, hydrocarbon oils (fatty acid ester oils, higher fatty acids, oils and fats, fluorinated oils are typical, and the components of the present invention ( Since it exhibits excellent compatibility and dispersibility with respect to A), it can be stably blended in the cosmetic composition of the present invention, can supplement the effects of the component (A), and can reinforce the specific effects of each. .
  • hydrocarbon oils examples include liquid paraffin, light liquid isoparaffin, heavy liquid isoparaffin, petrolatum, n-paraffin, isoparaffin, isododecane, isohexadecane, polyisobutylene, hydrogenated polyisobutylene, polybutene, ozokerite, ceresin, and microcrystalline wax.
  • paraffin wax polyethylene wax, polyethylene / polypropylene wax, squalane, squalene, pristane, polyisoprene and the like.
  • fatty acid ester oils include hexyldecyl octoate, cetyl octanoate, isopropyl myristate, isopropyl palmitate, butyl stearate, hexyl laurate, myristyl myristate, oleyl oleate, decyl oleate, octyldodecyl myristate, Hexyldecyl dimethyloctanoate, cetyl lactate, myristyl lactate, diethyl phthalate, dibutyl phthalate, lanolin acetate, ethylene glycol monostearate, propylene glycol monostearate, propylene glycol dioleate, glyceryl monostearate, glyceryl monooleate, Glyceryl tri-2-ethylhexanoate, trimethylolpropane tri-2-ethylhexanoate,
  • higher fatty acids examples include lauric acid, myristic acid, palmitic acid, stearic acid, behenic acid, undecylenic acid, oleic acid, linoleic acid, linolenic acid, arachidonic acid, eicosapentaenoic acid (EPA), docosahexaenoic acid (DHA), Examples include isostearic acid and 12-hydroxystearic acid.
  • a silicone oil agent and a non-silicone oil agent may be used in combination.
  • it retains the moisture of the hair and moisturizes the hair cosmetic composition of the present invention to moisturize the hair (also called “moist touch”)
  • a smooth feel can be imparted and the stability of the cosmetic over time is not impaired.
  • cosmetics containing hydrocarbon oils and / or fatty acid ester oils and silicone oils apply these moisturizing ingredients (hydrocarbon oils and / or fatty acid ester oils) in a more stable and uniform state on the skin or hair. Therefore, the moisturizing effect of the moisturizing component on the skin is improved.
  • cosmetics containing silicone oils together with non-silicone oils should give a smoother and moist feel. There is an advantage that can be.
  • fats and oils natural animal and vegetable oils and semi-synthetic fats and oils, such as avocado oil, linseed oil, almond oil, ibotarou, eno oil, olive oil, cacao butter, kapok wax, kaya oil, carnauba wax, liver oil, candelilla wax, beef tallow, hardened beef tallow , Kyonin oil, whale wax, hydrogenated oil, wheat germ oil, sesame oil, rice germ oil, rice bran oil, sugarcane wax, sasanqua oil, safflower oil, shea butter, cinnamon oil, cinnamon oil, jojo barrow, olive squalane, shellac wax, Turtle oil, soybean oil, tea seed oil, camellia oil, evening primrose oil, corn oil, lard, rapeseed oil, Japanese kiri oil, nukarou, germ oil, horse fat, persic oil, palm oil, palm kernel oil, castor oil, Hydrogenated castor oil, castor oil fatty acid methyl ester, sunflower
  • fluorinated oil examples include perfluoropolyether, perfluorodecalin, and perfluorooctane.
  • One or more of these oil agents can be used, and are contained in an amount of 0.1 to 30% by weight, preferably 0.5 to 10% by weight, based on the total composition of the cosmetic. If it is less than 0.1% by weight, a sufficient effect corresponding to the purpose of blending the oil cannot be obtained, and if it exceeds 30% by weight, the film-forming property of the cosmetic is not good even if the component (A) is used. Sufficient and easy to break up makeup.
  • hydrophilic fine particles optionally used in the cosmetic of the present invention may be treated with one or more materials and may be surface-coated with a hydrophilic substance.
  • hydrophilic treatment materials include hydrophilic polymers, cellulose, agar, deoxyribonucleic acid, lecithin, surfactants, inorganic materials such as polyacrylic acid, silica, alumina, or zirconia, preferably multiple processes or treatments. It is used for imparting hydrophilicity to fine particles through the process.
  • Hydrophilic fine particles can take any shape (spherical, rod-like, needle-like, plate-like, irregular shape, flake-like, spindle-like, etc.) and any state (smog, fine particles, pigment, etc.). Any particle structure (porous or non-porous) can be taken.
  • the hydrophilic fine particles may be inorganic powder or organic powder, surfactant metal salt fine particles, colored pigment, pearl pigment, metal powder pigment.
  • Examples of hydrophilic fine particles include silica hydrate, zinc oxide, titanium dioxide, cerium oxide, zirconium dioxide, aluminum hydroxide, sodium metaphosphate, and cellulose. Preferably, zinc oxide or titanium dioxide or cerium oxide is used.
  • hydrophilic fine particles have a sun blocking effect or a reflection effect, and can protect the skin from UV.
  • the content of hydrophilic fine particles in the emulsion is 0.10 to 70% by weight, preferably 0.20 to 50% by weight, more preferably 0.30 to 30% by weight.
  • hydrophilic fine particles examples include Cosmeserve WP-40W (Dainippon Kasei Co., Ltd.), FINEX-50W (Sakai Chemical Industry Co., Ltd.), FINEX-30W (Sakai Chemical Industry Co., Ltd.), ST-455WS (Titanium Industry Co., Ltd.) Company), ST-495M (Titanium Industry Co., Ltd.), TTO-S-1 (Ishihara Sangyo Co., Ltd.), TTO-S-3 (Ishihara Sangyo Co., Ltd.), TTO-V-3 (Ishihara Sangyo Co., Ltd.), MT -There are 150W (Taika Corporation), MT-100AQ (Taika Corporation), and MT-100WP (Taika Corporation).
  • the cosmetics of the present invention are usually used in cosmetics, for example, other oily substances, pigments, antioxidants, fragrances, dyes, preservatives, thickeners, pH adjusters, blood circulation
  • An accelerator, a cooling agent, an antiperspirant, a disinfectant, a skin activator, a moisturizer, a refreshing agent and the like can be contained within a qualitative and quantitative range that does not impair the object and effect of the present invention.
  • the types of cosmetics and the forms of the preparations are not particularly limited, and skin care products such as skin care products, antiperspirant products, deodorant products, makeup products, UV protection products, eyelash cosmetic products, Hair cosmetic products such as hair cleaning products, hair styling products, hair coloring products, hair nourishing products, hair rinse products, hair conditioner products, hair treatment products, etc .; hair cosmetic products such as bath cosmetics.
  • the form is not particularly limited, but is in the form of solution, emulsion, cream, solid, semi-solid, paste, gel, powder, multilayer, mousse, water-in-oil or oil-in-water. Any emulsified composition (emulsion composition) may be used.
  • the external preparation is applied to human skin, nails, hair, and the like.
  • a pharmaceutical active ingredient can be blended and used for treatment of various diseases.
  • Cosmetics are also applied to human skin, nails, hair, etc., but are used for cosmetic purposes. Even if it is used as an “external preparation”, it is actually used in the same usage and dosage as cosmetics. Therefore, in the cosmetics in this application, it describes as including such an external preparation as cosmetics. Examples thereof include antiperspirants, skin cleansers, skin external preparations, hair cleansers, hair external preparations and the like.
  • Examples of the use of the external preparation as a drug include, but are not limited to, hair growth agents, hair growth agents, analgesics, bactericides, anti-inflammatory agents, refreshing agents, and skin antiaging agents.
  • the cosmetic composition according to the present invention contains the component (A), a film excellent in water repellency and excellent in durability and sebum durability can be formed on the skin or hair.
  • the cosmetic composition of the present invention since the cosmetic composition of the present invention has a form emulsified with a cationic surfactant, it forms a film that is blended particularly in hair cosmetics compared to a dosage form emulsified with an anionic surfactant. It has excellent blending stability with components and can form a stable film over a long period of time. As a result, it is possible to improve the retainability (hair setting power), volume feeling, and unity feeling of hair and the like, and there is an advantage that styling property and shape retainability can be improved particularly under high humidity.
  • the present invention can also be used as a film forming agent in addition to cosmetic compositions and cosmetics.
  • the film can be used in any field as long as the film is required to have a water-repellent effect, an oil-repellent effect, uniformity, strength, and a rubbing system.
  • it can also be used as an agent for imparting a water repellent effect to a coating composition or fiber, or a treatment agent for inorganic or organic materials.
  • the film forming agent of the present invention can be used in an aqueous environment, it is very easy to handle.
  • the film-forming agent according to the present invention in particular, the component (A) (B) cationic surfactant and (Y) water-soluble azo radical initiator.
  • the film-forming agent containing a vinyl polymer has excellent blending stability with a cationic compounding component such as a cationic surfactant, and the film-forming property and feeling of use are not impaired. It can also be suitably used as a film forming agent for industrial use used as a treating agent.
  • the viscosity is a measured value at 25 ° C.
  • the part representing the blending amount in the table and the like means part by weight
  • % representing the content means weight%.
  • a contact angle meter (DSA Mk2) manufactured by KRUSS was used. (Evaluation of sebum resistance) This was performed in the same manner as the water resistance evaluation, except that the contact angle was measured using artificial sebum instead of water droplets. (Weight average molecular weight) The weight average molecular weight in terms of polystyrene was measured by gel permeation chromatography using tetrahydrofuran as a solvent.
  • Example 1 (Monomer emulsification) An emulsifier (polyoxyethylene tridecyl ether / ethylene oxide unit (EO) 15 mol adduct: 0.50 parts by weight, 30% by weight aqueous solution of cetyltrimethylammonium chloride: 1.93 parts by weight) was measured in beaker 1, Exchange water: 54.07 parts by weight was added and stirred to obtain an aqueous solution.
  • EO polyoxyethylene tridecyl ether / ethylene oxide unit
  • Example 2 (Monomer emulsification) A monomer emulsion was obtained in the same manner as in Example 1 except that the raw materials mixed in the beakers 1 and 2 were changed as follows.
  • the mixture of beaker 2 was added to beaker 1 and stirred for 3 to 10 minutes until uniform, and then passed three times with a homogenizer at a pressure of 300 to 400 Kg / cm 2 to obtain a milky white monomer emulsion having an average particle diameter of 174 nm. It was. (Radical polymerization) A separable flask was charged with 1/3 amount of the above monomer emulsion, heated to 65 ° C. while stirring, and after reaching 65 ° C., the remaining 2/3 amount of monomer emulsion and 0.40 weight were obtained.
  • emulsifier polyoxyethylene tridecyl ether / ethylene oxide unit (EO) 15 mol adduct: 0.50 parts by weight, 30% aqueous solution of cetyltrimethylammonium chloride: 1.93 parts by weight, ion-exchanged water: 54.12 parts by weight was added and stirred to obtain an aqueous solution.
  • emulsifier polyoxyethylene tridecyl ether / ethylene oxide unit (EO) 15 mol adduct: 0.50 parts by weight
  • 30% aqueous solution of cetyltrimethylammonium chloride 1.93 parts by weight
  • ion-exchanged water 54.12 parts by weight
  • the mixture of beaker 2 was added to beaker 1 and stirred for 3 to 10 minutes until uniform, and then passed three times with a homogenizer at a pressure of 300 to 400 Kg / cm 2 to obtain a milky white monomer emulsion having an average particle size of 158 nm. It was. (Radical polymerization)
  • the raw materials charged into the separable flask were changed as follows, and 1/3 of the obtained monomer emulsion was charged and heated to 70 ° C. with stirring. After reaching 70 ° C., the remaining 2/3 amount of the resulting monomer emulsion and 0.25 parts by weight of 2,2′-azobis (2-methylpropionamidine) dihydrochloride were prepared with ion-exchanged water.
  • Aqueous solution 12.51 parts by weight were gradually added dropwise and reacted at 70 ° C. for 2 hours, then heated to 80 ° C. and reacted at 80 ° C. for 3 hours. (result) After the reaction, there was no smell of methyl methacrylate or butyl acrylate.
  • the completed emulsion had an average particle size of 116 nm and a non-volatile content of approximately 25%, confirming that the reaction was complete.
  • a contact angle value was measured as an index for measuring film physical properties.
  • the contact angle is small, the contact area between the film and water or sebum increases, which causes a weakening of the film such as swelling.
  • the contact angle is high, the contact area is small and the influence on the film is small.
  • a high contact angle value means that the water resistance and sebum resistance properties are highly durable. Inevitably, the friction resistance and the adhesion (sustainability) on the hair are also high.
  • Examples 1 and 2 and Synthesis Example 1 show a contact angle of 100 ° or more in water contact angle, and a sufficiently high value in artificial sebum. Since Comparative Example 1 does not contain a carbosiloxane dendrimer component, it is very weak in water resistance and sebum resistance characteristics. Comparative Example 2 contains a carbosiloxane dendrimer component and is excellent in water resistance and sebum resistance properties. However, since the emulsifier is anionic, it reacts with the cationic component contained in the hair preparation and blending stability is impaired.
  • Example 6 is an Example obtained using the cosmetic composition of Synthesis Example 1 synthesized using a nonionic surfactant and the cationic surfactant (B phase).
  • a hair mist of a type (leave-on) that does not wash away with the composition (parts by weight) shown in the following table was prepared by the following production method.
  • the blending stability was evaluated by the following method and shown in the same table.
  • Neo Sol Acryo * 8 Narco Sensomer CI-50 Warm Phase A to 80 ° C. to completely dissolve.
  • Examples 7 and 8 according to the present invention are excellent in the blending stability of the cosmetic composition and excellent in the feel of hair mist, film formation and water repellency on the hair.
  • Comparative Examples 4 and 6 having no dendrimer structure the blending stability was not impaired, but film formation, water repellency and feel on the hair were not improved or insufficient.
  • Comparative Example 5 containing no cationic surfactant the blending stability of the polymer was insufficient, and a stable formulation could not be realized.
  • composition (wt%) Phase A Cetearyl alcohol 3 Cetearyl alcohol, behentrimonium chloride * 1 5.5 Silicone oil mixture * 2 3 Phase B Water residue EDTA-2Na 0.1 Polyquaternium-10 0.5 Behentrimonium sulfate 2 Phase C Panthenol 0.3 Glycerin 5 Piroctone olamine (bactericidal agent) 0.5 Aminosilicone emulsion * 33 Phase D 12 Preservative appropriate amount13. Perfume appropriate amount14.
  • Example 1 Cosmetic composition of Example 1 4 * 1 Crocro Incroquat Behenyl TMC-25 * 2 DOW CORNING (R) CB-3046 FLUID made by Toray Dow Corning * 3 DOW CORNING (R) CE-8411 SMOOTH PLUS EMULSION made by Toray Dow Corning (Production method) Heat Phase A to 80 ° C. Heat Phase B to 80 ° C and dissolve completely. While stirring Phase B, slowly add Phase A and emulsify. Cool to below 50 ° C and add Phase C and D ingredients. Stir until everything is uniform.
  • Example 2 Cosmetic composition of Example 2 10 * 1 Solubilisant LRI manufactured by Sensient Cosmetic Technologies * 2 DOW CORNING (R) CE-7080 SMART STYLE manufactured by Toray Dow Corning * 3 XIAMETER (R) OFX-0193 FLUID manufactured by Toray Dow Corning (Production method) Warm Phase A to 65 ° C. Add Phase B to 1 above and mix. Cool to room temperature. Add Phase C to 3 above and mix.
  • composition (wt%) Phase A Emulsifier premix * 1 4 Cetyl alcohol 2 Dialkyl malate (C12,13) 0.5 Phase B Shea fat 1.5 Black currant seed oil 1 Argan oil 0.5 Phase C Water Residual cetrimonium chloride 1 Phase D Preservative Appropriate amount of active ingredient mixture for hair * 21 Aminosilicone emulsion * 32 Perfume Appropriate amount Cosmetic composition of Synthesis Example 1 4 * 1 Evipon HC manufactured by Eigenmann & Veronelli * 2 Solair's HAIRSPHERE AG * 3 DOW CORNING (R) CE-8411 SMOOTH PLUS EMULSION made by Toray Dow Corning (Production method) 1.
  • composition (wt%) Phase A Water residue EDTA-2Na 0.1 Panthenol 0.5 PG (Cosmetic label) 5 PEG / PPG-8 / 3 lauric acid 1.5 Laurylmethylgluces-10 hydroxypropyldimonium chloride 1.5 Cetrimonium chloride 2 Water, BG, glycosphingolipid * 1 0.3 Silicone wax * 2 2 Phase B 10. Aminosilicone emulsion * 3 3 Phase C 11. Perfume appropriate amount 12. Preservative appropriate amount13.
  • composition (wt%) Phase A Cetyl alcohol 3 Stearyl alcohol 3 Behentrimonium chloride 1 Shea fat 1 Phase B Polyquaternium-67 0.2 PEG-45M (Cosmetic label) 0.05 Aminosilicone emulsion * 11.75 Hydroxyethyl cellulose 1 Panthenol 0.2 Linseed oil 0.2 Apricot kernel oil 0.2 Perfume Appropriate amount of water Residual preservative Appropriate amount of glycerin 5 Phase C Cosmetic composition of Example 2 6 * 1 DOW CORNING (R) CE-8411 SMOOTH PLUS EMULSION (Production method) Warm Phase A to 80 ° C. Warm Phase B to 80 ° C. While stirring Phase B, add Phase A and emulsify. Cool to room temperature. Add Phase C and mix until uniform.
  • composition (wt%) Phase A Behentrimonium chloride 2 Cetearyl alcohol 5 Water residue Phase B Silicone oil * 1 2 High polymerization silicone oil * 22 Amino-modified silicone * 3 1 Phase C Preservative Suitable amount perfume Suitable amount Cosmetic composition of Synthesis Example 1 5 * 1 XIAMETER (R) PMX-200 SILICONE FLUID 350CS manufactured by Toray Dow Corning * 2 XIAMETER (R) PMX-1503 FLUID manufactured by Toray Dow Corning * 3 DOW CORNING (R) AP-8087 FLUID made by Toray Dow Corning (Production method) Warm Phase A to 80 ° C. While stirring Phase A, add Phase B and emulsify. Cool 2 while stirring. Add Phase C and stir until uniform.
  • Example 7 Cleansing Conditioner] (Composition) (wt%) Phase A Water residual behentrimonium chloride 2 Cetearyl alcohol 5 Phase B Hydroxypropyl starch phosphate * 1 2 Phase C Highly polymerized silicone emulsion * 23.33 Preservative appropriate amount bactericidal agent (Piroctone olamine) 0.3 Phase D Emulsifier premix * 3 1 Cosmetic composition of Example 1 3 Phase E 10. Citric acid 50% aqueous solution * 1 Structure XL from National Starch & Chemical Company * 2 DOW CORNING (R) HMW 2220 NON-IONIC EMULSION manufactured by Toray Dow Corning * 3 Genagen 3SB manufactured by Clariant (Production method) Warm Phase A to 85 ° C. Slowly add Phase B to 1 above and mix until uniform. Cool to 40 ° C or lower with stirring. Add Phase C while stirring 3 above. Add Phase D while slowly stirring 4 above. Add Phase E so that the pH is 4.5-5.0.
  • Example 2 Cosmetic composition of Example 2 3 * 1 Jaguar C13-S manufactured by Rhodia * 2 DOW CORNING (R) CE-1689 SMOOTHING EMULSION made by Toray Dow Corning * 3 DOW CORNING (R) HMW 2220 NON-IONIC EMULSION manufactured by Toray Dow Corning * 4 Soothing Milk manufactured by Solabia (Production method) Warm Phase A to 80 ° C. Warm Phase B to 80 ° C. Add Phase A while stirring Phase B. Cool to 45 ° C or lower with stirring. Add Phase C to 4 above and stir until uniform. Add Phase D to 5 above and stir until uniform.
  • composition (wt%) Phase A Hydroxyethyl cellulose 1.5 EDTA-4Na 0.1 Water residue Phase B Cetearyl alcohol 2 Stearamidopropyldimethylamine 1 Phase C Silicone quaternary ammonium salt emulsion * 1 2.3 Amino-modified silicone emulsion * 2 1.8 Preservative appropriate amount Cosmetic composition 2 of Synthesis Example 1 * 1 DOW CORNING (R) 5-7113 SILICONE QUAT MICROEMULSION made by Toray Dow Corning * 2 DOW CORNING (R) CE-8411 SMOOTH PLUS EMULSION made by Toray Dow Corning (Production method) Warm Phase A to 75 ° C. Add Phase B while stirring Phase A. Cool until below 40 ° C. Add Phase C and mix.
  • the present invention is used as a film-forming agent in cosmetic compositions and cosmetics containing a cationic surfactant and a base material, but is not limited thereto, and can be used in other applications and products. That is, it can be used not only in the field, but in applications where the film is required to have a water repellency effect, an oil repellency effect, uniformity, strength, rub resistance and flexibility. In particular, it is also used as a surface active agent including a cationic surfactant or a base material, a water repellent effect imparting agent for fibers, fabrics, woven fabrics, or the like, or a processing agent or protective agent for inorganic materials / organic materials. Moreover, since the film-forming agent of the present invention can be used in an aqueous environment, it is used as a main agent or additive in an aqueous composition.

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Abstract

[Problème] La présente invention vise à fournir un produit cosmétique, ou un agent filmogène, qui, même lorsqu'il est utilisé en tant que produit cosmétique pour utilisation sur les cheveux, ou un agent filmogène pour utilisation sur des fibres comprenant des cheveux, peut atteindre d'excellentes propriétés de formation de film, facilité d'utilisation et stabilité de formulation, et qui utilise un polymère vinylique ayant une structure de dendrimère carbosiloxane dans la chaîne latérale. [Solution] La présente invention concerne une composition cosmétique ou un agent filmogène qui est une composition qui contient (A) 100 parties en poids d'au moins un polymère vinylique ayant au moins une structure de dendrimère de carbosiloxane dans une chaîne latérale, (B) 0,1 à 30 parties en poids d'un tensioactif cationique, et (X) de l'eau, des particules émulsifiées formées à partir d'au moins le composant (A) et le composant (B) étant dans une phase aqueuse, et le poids moléculaire moyen en poids du composant (A) étant d'au moins 80 000.
PCT/JP2018/010181 2017-04-06 2018-03-15 Composition cosmétique, produit cosmétique et agent filmogène Ceased WO2018186138A1 (fr)

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WO2020142474A1 (fr) 2018-12-31 2020-07-09 Dow Silicones Corporation Composé d'organosilicium ramifié à fonction acrylate, son procédé de préparation et copolymère formé avec celui-ci
WO2020142441A1 (fr) 2018-12-31 2020-07-09 Dow Silicones Corporation Composé organosilicié ramifié, procédé pour sa préparation et copolymère formé avec celui-ci
WO2020142370A1 (fr) 2018-12-31 2020-07-09 Dow Silicones Corporation Composé d'organosilicium ramifié, son procédé de préparation et copolymère formé avec celui-ci
WO2020142388A1 (fr) 2018-12-31 2020-07-09 Dow Silicones Corporation Composition, procédé de préparation d'un copolymère, et procédés et utilisations finales associés
EP3967291A1 (fr) * 2020-09-15 2022-03-16 Unilever Global IP Ltd Composition capillaire
US20220175653A1 (en) * 2019-04-18 2022-06-09 Dow Global Technologies Llc An aminosiloxane/alkyl silane blend
WO2024113195A1 (fr) 2022-11-30 2024-06-06 Dow Toray Co., Ltd. Particule solide de copolymère à fonction organosilicium, son procédé de fabrication, et produit cosmétique comprenant ladite particule solide
US12215198B2 (en) 2018-12-31 2025-02-04 Dow Silicones Corporation Branched organosilicon compound, method of preparing same, and compositions comprising same
US12215117B2 (en) 2018-12-31 2025-02-04 Dow Silicones Corporation Method of preparing acryloxy-functional organosilicon compounds
US12269833B2 (en) 2018-12-31 2025-04-08 Dow Silicones Corporation Branched organosilicon compound, method of preparing same, and compositions comprising same

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JP2011149017A (ja) * 2009-12-24 2011-08-04 Dow Corning Toray Co Ltd カルボシロキサンデンドリマー構造を有する共重合体、並びに、それを含む組成物及び化粧料
JP2014114270A (ja) * 2012-10-03 2014-06-26 Kose Corp 毛髪化粧料
WO2017061090A1 (fr) * 2015-10-09 2017-04-13 東レ・ダウコーニング株式会社 Agent filmogène, et composition cosmétique et produit cosmétique utilisant celui-ci

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JP2001192424A (ja) * 1999-10-29 2001-07-17 Dow Corning Toray Silicone Co Ltd シリコーングラフトビニル系共重合体エマルジョン組成物
JP2011149017A (ja) * 2009-12-24 2011-08-04 Dow Corning Toray Co Ltd カルボシロキサンデンドリマー構造を有する共重合体、並びに、それを含む組成物及び化粧料
JP2014114270A (ja) * 2012-10-03 2014-06-26 Kose Corp 毛髪化粧料
WO2017061090A1 (fr) * 2015-10-09 2017-04-13 東レ・ダウコーニング株式会社 Agent filmogène, et composition cosmétique et produit cosmétique utilisant celui-ci

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US11820846B2 (en) 2018-12-31 2023-11-21 Dow Silicones Corporation Composition, method of preparing copolymer, and methods and end uses thereof
US12269833B2 (en) 2018-12-31 2025-04-08 Dow Silicones Corporation Branched organosilicon compound, method of preparing same, and compositions comprising same
WO2020142370A1 (fr) 2018-12-31 2020-07-09 Dow Silicones Corporation Composé d'organosilicium ramifié, son procédé de préparation et copolymère formé avec celui-ci
WO2020142388A1 (fr) 2018-12-31 2020-07-09 Dow Silicones Corporation Composition, procédé de préparation d'un copolymère, et procédés et utilisations finales associés
US12398270B2 (en) 2018-12-31 2025-08-26 Dow Silicones Corporation Acrylate-functional branched organosilicon compound, method of preparing same, and copolymer formed therewith
US12338259B2 (en) 2018-12-31 2025-06-24 Dow Silicones Corporation Branched organosilicon compound, method of preparing same, and copolymer formed therewith
US12215198B2 (en) 2018-12-31 2025-02-04 Dow Silicones Corporation Branched organosilicon compound, method of preparing same, and compositions comprising same
US12371535B2 (en) 2018-12-31 2025-07-29 Dow Silicones Corporation Branched organosilicon compound, method of preparing same, and copolymer formed therewith
WO2020142441A1 (fr) 2018-12-31 2020-07-09 Dow Silicones Corporation Composé organosilicié ramifié, procédé pour sa préparation et copolymère formé avec celui-ci
US12215117B2 (en) 2018-12-31 2025-02-04 Dow Silicones Corporation Method of preparing acryloxy-functional organosilicon compounds
WO2020142474A1 (fr) 2018-12-31 2020-07-09 Dow Silicones Corporation Composé d'organosilicium ramifié à fonction acrylate, son procédé de préparation et copolymère formé avec celui-ci
US20220175653A1 (en) * 2019-04-18 2022-06-09 Dow Global Technologies Llc An aminosiloxane/alkyl silane blend
EP3967291A1 (fr) * 2020-09-15 2022-03-16 Unilever Global IP Ltd Composition capillaire
WO2024113195A1 (fr) 2022-11-30 2024-06-06 Dow Toray Co., Ltd. Particule solide de copolymère à fonction organosilicium, son procédé de fabrication, et produit cosmétique comprenant ladite particule solide

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