JP4731382B2 - Water-in-oil emulsified cosmetic - Google Patents

Description

  The present invention blends a resin with good adhesion to the skin and excellent gas permeability, so that excellent adhesion, makeup durability, no burden on the skin, and smooth stretch spread. The present invention relates to a water-in-oil emulsified cosmetic having excellent stability over time.

Water-in-oil emulsified cosmetics are superior in water resistance and sweat resistance compared to oil-in-water emulsified cosmetics, and are used in various cosmetics and are becoming mainstream in recent years. However, water-in-oil emulsified cosmetics have an oily component in the outer layer, so they have a smooth touch and spread, and you can expect a moist feeling and emollient effect, but they feel oily and sticky. There was a defect, and a refreshing feel could not be obtained. In addition, makeup persistence may be reduced because it easily mixes with sebum secreted over time.
Therefore, a technique for improving the sustainability and storage stability of the cosmetic effect by blending volatile silicone oil or silicone resin has been studied (for example, see Patent Document 1). In addition, there is a technique for improving the stability and feeling of use of a perfluoro organic compound by using a fluorine-based polymer as a perfluoro organic compound having sebum resistance and oil resistance (see, for example, Patent Document 2). Furthermore, a technique for improving the sun protection effect while reducing secondary adhesion using a volatile component, an organically modified clay mineral, a spherical resin powder, and a film forming agent has been studied (for example, see Patent Document 3).

JP-A-7-309714 JP-A-8-59448 Japanese Patent Laid-Open No. 9-255543

  Since cosmetics including water-in-oil emulsified cosmetics have movement in the application part, it is important that the cosmetic film does not follow the movement and does not move (run) or collapse. In addition, since water-in-oil emulsified cosmetics contain a wide variety of components depending on the purpose, compatibility with other components is also an important factor. In water-in-oil emulsified cosmetics, many studies have been made on the blending of adhesiveness, water resistance, and oil resistance resin, but there are not many studies on resins having air permeability. Therefore, although the resin itself has water resistance and oil resistance, when it is blended in cosmetics, the cosmetic durability may not be improved as expected. Therefore, it has higher breathability, has excellent skin adhesion and makeup sustainability, has no sense of burden on the skin, can smoothly spread and form a uniform and thin makeup coating, and has good stability over time. Development of water-in-oil emulsified cosmetics has been desired.

  In view of such circumstances, the present inventors have intensively studied, and as a result, have a bulky structure in order to provide more space in the molecular structure of a silicone resin that has been considered to have high gas permeability and is highly safe. By introducing a specific amount of monomer, a cosmetic component having excellent makeup durability and no burden on the skin by blending a resin component with further improved compatibility with the cosmetic component and gas permeability It came to embody.

That is, the present invention provides the following components (A) to (D);
(A) 55-65 mass% of monomer (a) shown by the following general formula (1)

(In the formula, R ¹ is H or CH ₃ , and p is an integer of 2 to 6)
Monomer (b) represented by the following general formula (2): 20 to 30% by mass

(In the formula, R ² is H or CH ₃ , and R ³ is an alkyl group having 1 to 5 carbon atoms or a phenyl group.)
As a monomer (c), acrylic acid and / or methacrylic acid 15-20 mass%
Water-in-oil containing a siloxy group-containing (meth) acrylic acid copolymer (B), a volatile silicone (C) and a silicone surfactant having a polyoxyethylene chain of 10 or less HLB. The present invention relates to a type emulsified cosmetic.

  The present invention relates to a water-in-oil emulsified cosmetic having excellent adhesion to the skin, makeup persistence, no feeling of burden on the skin, smooth spreading, and excellent stability over time. .

Hereinafter, the present invention will be described in detail.
The monomer (a) constituting the siloxy group-containing (meth) acrylic acid copolymer of component (A) used in the oil-in-water emulsion cosmetic of the present invention is a component that imparts gas permeability to the copolymer It has been conventionally used for a contact lens material, and its structure is represented by the following general formula (1).

(In the formula, R ¹ is H or CH ₃ , and p is an integer of 2 to 6)

  Preferable examples of the monomer (a) include tris (trimethylsiloxy) silylpropyl methacrylate, tris (trimethylsiloxy) silylpropyl acrylate, tris (trimethylsiloxy) silylhexyl methacrylate and the like, and particularly tris (trimethylsiloxy) silylpropyl. Methacrylate is preferred. The monomer (a) is not particularly limited, and various commercially available products can be used.

  The monomer (b) is a component that imparts appropriate hardness and flexibility to the copolymer and compatibility with other cosmetic ingredients, and its structure is represented by the following general formula (2).

(In the formula, R ² is H or CH ₃ , and R ³ is an alkyl group having 1 to 5 carbon atoms or a phenyl group.)

  Preferable examples of the monomer (b) include methyl methacrylate, ethyl methacrylate, phenyl acrylate and the like, and methyl methacrylate is particularly preferable. The monomer (b) is not particularly limited, and various commercially available products can be used.

  The monomer (c) is acrylic acid and / or methacrylic acid, and is a component for improving the film-forming property of the copolymer and imparting hydrophilicity. In the copolymer of the component (A), cosmetics are used. In view of solubility in the oil for use as a material, methacrylic acid is preferred.

  Component (A), a siloxy group-containing (meth) acrylic acid copolymer, is charged with these monomers in the amount of (a) 55 to 65% by mass (hereinafter simply referred to as “%”), (b). It is obtained by adding 20 to 30% and (c) 15 to 20% and copolymerizing. In addition to the above monomers (a) to (c), a monomer copolymerizable with (meth) acrylic acid ester is optionally added within the range not impairing gas permeability and film-forming properties. It may be polymerized.

  Examples of the polymerization method for component (A) include a solution polymerization method in which each monomer is dissolved in a solvent, a polymerization initiator is added, and the mixture is heated and stirred in a nitrogen atmosphere. Solvents used in the polymerization method include alcohols such as methanol, ethanol, propanol and butanol, ketones such as acetone, methyl ethyl ketone and diethyl ketone, esters such as ethyl acetate and butyl acetate, aromatic solvents such as benzene, toluene and xylene. These may be used by appropriately mixing them. The polymerization reaction can be usually carried out within a temperature range of 50 to 180 ° C., preferably 60 to 120 ° C., and can be completed in about 5 to 15 hours under these conditions.

  In the present invention, as a preferred embodiment of the method for producing a siloxy group-containing (meth) acrylic acid copolymer, first, tris (trimethylsiloxy) silylpropyl methacrylate, methacrylic acid and methyl methacrylate, butyl acetate, ethyl acetate Then, a solvent such as isopropanol and a polymerization initiator such as 2,2′-azobisisobutyronitrile are placed in a reaction vessel such as a flask, and dissolved oxygen in the reaction vessel is removed by nitrogen gas bubbling or the like and sealed. Next, there is a method in which the reaction vessel is transferred into a constant temperature bath and polymerization is performed for about 15 hours while stirring at about 60 ° C.

  The siloxy group-containing (meth) acrylic acid copolymer produced in this way has a weight average molecular weight in terms of polystyrene in GPC of about 3,000 to about 200,000, particularly about 5,000 to about 100,000. It is preferably in the range of 000, and preferably has a glass transition temperature in the range of -30 to + 60 ° C.

  Examples of such a siloxy group-containing (meth) acrylic acid copolymer of component (A) include those having a structure represented by the following chemical formula (3).

(Here, x in the formula is an integer of 35 to 50, y is 20 to 30 integer, z is an integer of 30 to 40, ^{R 4} is a group represented by the following chemical formula (4).)

In the water-in-oil emulsified cosmetic of the present invention, the amount of the component (A) siloxy group-containing (meth) acrylic acid copolymer is not particularly limited, but is 0.1 to 30%, more preferably 1. ~ 15%. Within this range, it is possible to obtain a water-in-oil emulsified cosmetic excellent in good adhesion, makeup sustainability, no feeling of burden on the skin, and smooth stretch spread.
As a method for blending the siloxy group-containing (meth) acrylic acid copolymer of component (A) into a water-in-oil emulsified cosmetic, for the convenience of handling, an oil agent blended into the cosmetic, for example, decamethylcyclo It is desirable to use it by pre-dissolving in an oil agent such as silicone oil such as pentasiloxane, dimethylpolysiloxane and methylphenylpolysiloxane, isopropyl alcohol, ethyl alcohol and light liquid isoparaffin.

As the volatile silicone of component (B) used in the present invention, any volatile silicone that is usually used in cosmetics can be used. For example, dimethyl having a viscosity at 25 ° C. of 2 mm ² / s or less. Examples thereof include polysiloxane, methyltrimethicone, octamethylcyclotetrasiloxane, decamethylcyclopentasiloxane, dodecamethylcyclohexasiloxane and the like.

  The volatile silicone component (B) used in the present invention is preferably blended in an amount of 5 to 60%, more preferably 10 to 40%, in the water-in-oil emulsified cosmetic of the present invention. If it is used within this range, a refreshing feel and smooth usability can be obtained.

  The silicone surfactant having a polyoxyethylene chain having a component (C) HLB of 10 or less used in the present invention is a silicone-based polyoxyalkylene-modified organopolysiloxane, long-chain alkyl-containing polyoxyalkylene-modified organopolysiloxane, or the like. Surfactant is mentioned. For example, examples of the polyoxyalkylene-modified organopolysiloxane include those having the structures shown below. Commercially available products include ABIL EM97 (manufactured by Goldschmidt), SH-3772C, SH3775C (manufactured by Toray Dow Corning), KF-6012, KF-6015, KF-6016, KF-6017 (manufactured by Shin-Etsu Chemical Co., Ltd.) and the like can be suitably used.

[Wherein R ² represents an alkyl group having 1 to 5 carbon atoms or a phenyl group. R ³ represents —Q ¹ —O— (C ₂ H ₄ O) _h — (C ₃ H ₆ O) _i —R ⁴ (where Q ¹ represents a divalent hydrocarbon group having 1 to 5 carbon atoms. R ⁴ represents a hydrogen atom, an alkyl group having 1 to 5 carbon atoms, or an acetyl group, h is an integer of 1 to 50, and i is an integer of 0 to 50.) G ¹ and G ² are May be the same or different and each represents R ² or R ³ . j represents an integer of 0 to 150, and k represents an integer of 0 to 50. However, when k = 0, at least one of G ¹ and G ² is R ³ . ]

  Examples of the long-chain alkyl-containing polyoxyalkylene-modified organopolysiloxane include those having the structure shown below, and as a commercially available product, ABIL EM90 (manufactured by Goldschmidt) is particularly preferably used.

[Wherein, R ⁵ represents an alkyl group having 1 to ⁵ carbon atoms or a phenyl group. R ⁷ is represented by —Q ² —O— (C ₂ H ₄ O) _c — (C ₃ H ₆ O) _d —R ⁹ , and Q ² represents a divalent hydrocarbon group having 1 to 5 carbon atoms. R ⁹ represents a hydrogen atom, an alkyl group having 1 to 5 carbon atoms, or an acetyl group. c is an integer of 1-50, d is an integer of 0-50. R ⁶ is represented by — (C ₃ H ₆ O) _e —R ¹⁰ , e is an integer of 0 to 5, and R ¹⁰ is a hydrocarbon group of 6 to 16. l is an integer of 5 to 150, m is an integer of 5 to 40, and n is an integer of 2 to 40. ]

  The silicone-based surfactant having a polyoxyethylene chain having a component (C) HLB of 10 or less used in the present invention is incorporated in the water-in-oil emulsified cosmetic of the present invention in an amount of 0.5 to 10%, more preferably. Is preferably 1 to 6%. If it is used within this range, a sufficiently stable emulsification effect can be obtained without feeling the stickiness peculiar to the emulsifier. These silicone surfactants having a polyoxyethylene chain having an HLB of 10 or less can be used alone or in combination of two or more as required.

  In the present invention, in order to further improve the stability of the water-in-oil emulsified cosmetic of the present invention, it is preferable to blend an oil gelling agent of component (D). As the oil gelling agent, one or more selected from organically modified clay minerals, fumed hydrophobic silica, dextrin fatty acid ester, and fructooligosaccharide fatty acid ester can be used.

  The organically modified clay mineral is obtained by organically modifying a water-swellable clay mineral with dimethyl distearyl ammonium chloride and bromide, dimethylbenzyl stearyl ammonium chloride, bromide, or the like. The water-swellable clay mineral is a kind of colloidal hydrous aluminum silicate having a three-layer structure, specifically, natural or synthetic montmorillonite groups such as montmorillonite, laponite and hectorite, and sodium silicic mica, sodium or lithium. Synthetic mica known by the name of teniolite. As the water-swellable clay mineral, montmorillonite and hectorite are particularly preferable. Examples of commercially available products include Benton 27 and Benton 38 (made by Elementis). The amount to be blended for improving stability is 0.2 to 3%, more preferably 0.4 to 2%. If it is this range, sufficient effect will be acquired.

  The fumed hydrophobized silica is fine silica having a particle size of 5 to 50 nm, and its surface is hydrophobized with a treating agent such as dimethyldichlorosilane or dimethylpolysiloxane. Specifically, AEROSIL R-972, R-974, R976-S, RX-300 (manufactured by Nippon Aerosil Co., Ltd.), CAB-O-SIL TS-530 (manufactured by Cabot Corp.) and the like can be exemplified. The amount added for improving the stability is 0.2 to 5%, more preferably 0.4 to 3%. If it is this range, sufficient effect will be acquired.

  The dextrin fatty acid ester is an oil-soluble one having a carbon number of 8 to 24 (preferably 14 to 18) and a saturated or unsaturated fatty acid having an average polymerization degree of 10 to 50 (preferably 20 to 30). It is an ester compound with dextrin. Specific examples include dextrin palmitate, dextrin palmitate / 2-ethylhexanoate, dextrin stearate, dextrin palmitate / dextrin stearate, dextrin oleate, dextrin isopalmitate, dextrin isostearate, etc. Or 2 or more types can be used. Examples of commercially available products include dextrin palmitate (Leopard KL, Leopard TL) and palmitic acid / 2-ethylhexanoic acid dextrin (Leopard TT) (both manufactured by Chiba Flour Mills). The amount added for improving stability is 0.2 to 5%, more preferably 0.4 to 3%. If it is this range, sufficient effect will be acquired.

  Specific examples of fructooligosaccharide fatty acid esters include those described in JP-A-3-197409 and JP-A-2002-193732. An ester compound of a linear or branched saturated or unsaturated fatty acid having 8 to 32 carbon atoms and a fructooligosaccharide, and the average molecular weight of the fructooligosaccharide is preferably in the range of 300 to 10,000. The above can be used. Examples of commercially available products include Leo Pearl ISK (manufactured by Chiba Flour Mills). The amount added for improving the stability is 0.2 to 5%, more preferably 0.4 to 3%. If it is this range, sufficient effect will be acquired.

  The water-in-oil emulsified cosmetic of the present invention contains water in addition to the above components. In the water-in-oil emulsified cosmetic of the present invention, the amount of water is preferably 5 to 60%, more preferably 10 to 40%.

  In the cosmetic of the present invention, components that are usually used in cosmetics can be blended in addition to the essential components as long as the effects of the present invention are not hindered.

  The powder component is not particularly limited by the shape of a plate, spindle, needle, etc., particle size, particle structure such as porous, non-porous, etc., inorganic powders, glitter powders, organic Examples thereof include powders, pigment powders, and composite powders. Specifically, conch, ultramarine, bengara, yellow iron oxide, black iron oxide, titanium oxide, zinc oxide, aluminum oxide, cerium oxide, magnesium oxide, zirconium oxide, magnesium carbonate, calcium carbonate, chromium oxide, chromium hydroxide, Carbon black, anhydrous silicic acid, aluminum silicate, magnesium silicate, magnesium aluminum silicate, mica, synthetic mica, synthetic sericite, sericite, talc, kaolin, silicon carbide, barium sulfate, bentonite, smectite, boron nitride, etc. Inorganic powders, bismuth oxychloride, titanium mica, iron oxide coated mica, iron oxide mica titanium, organic pigment coated mica titanium, aluminum powder and other glittering powders, organic tar pigments, organic pigment lake pigments, etc. Dye powders, fine titanium oxide coated mica titanium, fine Zinc oxide coated mica titanium, barium sulfate coated mica titanium, titanium oxide containing silicon dioxide, zinc oxide containing silicon dioxide and other composite powders, magnesium stearate, zinc stearate, N-acyl lysine, spherical nylon powder, spherical polystyrene powder, Examples include spherical polymethacrylic sanmethyl powder, spherical silicone resin powder, polyethylene terephthalate / aluminum / epoxy laminated powder, polyethylene terephthalate / polyolefin laminated film powder, polyethylene terephthalate / polymethyl methacrylate laminated film powder, and the like. The above can be used. These powders may be used alone or in combination of two or more, and the surface is treated with an oil agent, a silicone compound, a fluorine compound, a metal soap, a surfactant, an amino acid compound. Alternatively, a water-soluble polymer treatment or the like may be applied.

  As the oil component, in addition to component (B), hydrocarbon oils such as light liquid isoparaffin, polybutene, liquid paraffin, squalane and isoparaffin, liquid oils such as liquid lanolin, ester oil, monoglyceride oil, diglyceride oil and triglyceride oil, paramethoxy UV absorbers such as 2-ethylhexyl cinnamate, semi-solid oils such as petrolatum and lanolin, paraffin wax, ceresin wax, microcrystalline wax, Fischer-Tropsch wax, polyethylene wax, polyethylene polypropylene copolymer, candelilla wax, carnauba wax, beads Solid oils such as wax, mole, and montan wax, oil-soluble resin components such as rosin acid pentaerythritol, N-lauroyl-L-glutamate di (phytostearyl, Non-volatile as an amino acid oil such as -octyldodecyl), N-lauroyl-L-glutamate di (cholesteryl / behenyl / octyldodecyl), N-lauroyl-L-glutamate di (cholesteryl / octyldodecyl), etc. In dimethylpolysiloxane, methylphenylpolysiloxane, dimethyldiphenylpolysiloxane, methoxyphenylpolysiloxane, methylhydrogenpolysiloxane, fluorine-based oils such as perfluoropolyether, trifluoropropyl octtetrasiloxane, trifluoropropyl cyclopentasiloxane And higher fatty acids such as stearic acid. The oil component is blended for the purpose of imparting emollient properties, realizing various usability, and protecting against ultraviolet rays.

  Examples of the surfactant include an anionic surfactant, a cationic surfactant, a nonionic surfactant other than the component (C), and an amphoteric surfactant. Specifically, anionic surfactants include fatty acid soaps, ether carboxylic acids and salts thereof, carboxylates such as condensation of amino acids and fatty acids, alkyl sulfonic acids, alkene sulfonates, sulfonates of fatty acid esters, fatty acids Amide sulfonates, sulfonates of alkyl sulfonates and their formalin condensates, alkyl sulfates, secondary higher alcohol sulfates, alkyl and aliether sulfates, sulfates of fatty acid esters, fatty acids Examples thereof include sulfate salts of alkylolamide, sulfate salts such as funnel oil, alkyl phosphates, ether phosphates, alkyl allyl ether phosphates, and amide phosphates. Nonionic surfactants include sorbitan fatty acid esters, polyoxyethylene sorbitan fatty acid esters, glycerin fatty acid esters, polyglycerin fatty acid esters, ethylene oxide derivatives of glycerin fatty acid esters, propylene glycol fatty acid esters, ethylene oxide derivatives of propylene glycol fatty acid esters. , Polyethylene glycol fatty acid ester, sucrose ester, polyoxyethylene alkyl ether, polyoxypropylene alkyl ether, polyoxyethylene alkylphenyl ether, polyoxyethylene castor oil derivative, polyoxyethylene hydrogenated castor oil derivative, polyoxyethylene phytostanol ether , Polyoxyethylene phytosterol ether, polyoxyethylene cholestanol ether Polyoxyethylene cholesteryl ether. Examples of amphoteric surfactants include lecithin.

  Other components include metal soaps for adjusting the feel, amino acid compounds, partially crosslinked organopolysiloxanes, and water-soluble polymers such as methylcellulose, hydroxymethylcellulose, alkyl-modified carboxyvinyl polymers, and carboxyvinyl polymers for the purpose of adjusting the feel in water. , Agar, locust bean gum, gellan gum, high methoxy pectin, low methoxy pectin, sclerotium gum, xanthan gum, guar gum, carrageenan, water-swelling clay minerals, other antioxidants, vitamins A, B6, B12, C, E Beauty ingredients such as vitamins and derivatives thereof, rosemary extract, chamomile extract, carrot extract, assembly extract, catechin, catechin derivative, licorice extract, Sakuhakuhi extract, hop extract, etc. Humectants such as gen, hyaluronic acid, hyaluronic acid derivatives, trehalose, aloe extract, refreshing agents such as menthol, camphor, sorbitol, ethanol, 1,3-butanediol, propylene glycol, dipropylene glycol, glycerin, diglycerin, etc. A polyhydric alcohol, a fragrance | flavor, etc. can be mix | blended.

  Examples of the water-in-oil emulsified cosmetic of the present invention include sunscreen cosmetics, foundations, base cosmetics, controls, eye colors, mascaras, lipsticks, eye colors, emulsions, cosmetics, creams and the like. Among them, eye color, sunscreen cosmetics, foundations, base cosmetics, milky lotions, creams have significant effects in terms of smoothness and ease of use because of the large movement and application area. Appears and is preferred. The properties may be any of liquid, emulsion, paste, cream, and solid.

  EXAMPLES Next, although an Example is given and this invention is demonstrated in detail, this invention is not limited to this.

Synthesis Example 1: Siloxy group-containing methacrylic acid copolymer solution 1
In a 500 mL flask, 55 parts of tris (trimethylsiloxy) silylpropyl methacrylate, 15 parts of methacrylic acid, 30 parts of methyl methacrylate, 110 parts of butyl acetate, 70 parts of ethyl acetate, 30 parts of isopropanol, 2,2'-azobisisobutyro 0.5 parts of nitrile was charged, and nitrogen gas was bubbled to remove dissolved oxygen and sealed. The reaction vessel was transferred to a thermostat and polymerization was carried out for 15 hours while stirring at 60 ° C. After completion of the polymerization, solvent substitution was performed on dimethylpolysiloxane (SH200C-6cs manufactured by Toray Dow Silicone Co., Ltd.) to obtain a siloxy group-containing methacrylic acid copolymer solution 1 (solid content concentration 20%).

Synthesis Example 2: Siloxy group-containing methacrylic acid copolymer solution 2
A 500 mL flask is charged with 60 parts of tris (trimethylsiloxy) silylpropyl methacrylate, 20 parts of methacrylic acid, 20 parts of methyl methacrylate, 100 parts of butyl acetate, 100 parts of ethyl acetate, 30 parts of isopropanol, and 1 part of dicumyl peroxide as a solvent. Nitrogen gas was bubbled to remove oxygen and sealed. The reaction vessel was transferred into a thermostat and polymerization was carried out over 6 hours while stirring at 60 ° C. After completion of the polymerization, the solvent was replaced with decamethylcyclopentasiloxane to obtain a siloxy group-containing methacrylic acid copolymer solution 2 (solid content concentration 20%).

Synthesis Example 3: Siloxy group-containing (meth) acrylic acid copolymer solution 3
In a 500 mL flask, 60 parts of tris (trimethylsiloxy) silylpropyl methacrylate as monomer components, 15 parts of methacrylic acid, 25 parts of methyl methacrylate, 110 parts of butyl acetate, 70 parts of ethyl acetate, 30 parts of isopropanol as a solvent, reaction initiator 2,2'-azobisisobutyronitrile 0.5 parts was charged. In order to remove dissolved oxygen, the flask was bubbled with nitrogen gas and sealed. The reaction vessel was transferred to a thermostat and polymerization was carried out for 15 hours while stirring at 60 ° C. After completion of the polymerization, the solvent was replaced with butyl acetate to obtain an acetic acid solution (solid content concentration 20%) of a siloxy group-containing (meth) acrylic acid copolymer solution. This siloxy group-containing (meth) acrylic acid copolymer had a structure represented by x = 45, y = 25, z = 30 in the chemical formula (3). The number average molecular weight in terms of polystyrene in GPC of this polymer was about 20,000.

Synthesis Comparative Example 1: Siloxy group-containing methacrylic acid copolymer solution 4
A 500 mL flask is charged with 50 parts of tris (dimethylsiloxy) silylpropyl methacrylate, 50 parts of methyl methacrylate, 110 parts of butyl acetate, 70 parts of ethyl acetate, 30 parts of isopropanol, and 0.5 part of dicumyl peroxide as a solvent to remove dissolved oxygen. For this purpose, nitrogen gas was bubbled and sealed. The reaction vessel was transferred into a constant temperature bath, and polymerization was carried out over 8 hours while stirring at 50 ° C. After completion of the polymerization, the solvent was replaced with decamethylcyclopentasiloxane to obtain a siloxy group-containing methacrylic acid copolymer solution 4 (solid content concentration 20%).

Examples 1 to 5 and Comparative Examples 1 to 4: Eye color Eye colors of the prescription shown in Table 1 were prepared by the following production method, adhesion to the skin, makeup persistence, no burden on the skin, Table 1 shows the results of evaluating smooth usability and stability over time.

(Note 1) BY11-018 (Toray Dow Corning) (solid content 30%)
(Note 2) DC593 (Toray Dow Corning) (solid content 33%)
(Note 3) ABIL EM-90 (HLB = 4.5) (Gold Schmidt)
(Note 4) SH3771M (HLB = 13) (Toray Dow Corning)
(Note 5) SA-Titanium CR50 (80%) (manufactured by Miyoshi Kasei)
(Note 6) SA-talc K-5μ (manufactured by Miyoshi Kasei)
(Note 7) SA-Timilon Splendid Gold (manufactured by Miyoshi Kasei)
(Production method)
A: Components 1 to 18 are mixed uniformly with a homomixer.
B: Components 19 to 25 were uniformly dissolved and mixed, then added to A, emulsified, defoamed, and then filled into a resin container with an applicator to obtain an eye color.

(Evaluation methods)
Regarding “adhesion to skin”, “make-up sustainability”, “no burden on skin”, and “smooth stretch and spread”, each eye color sample was tested by 20 specialist panels. Each person gave a rating based on the following absolute evaluation and assigned a score. The average value was calculated from the total score of all the panel members for each sample, and the determination was made according to the following four-step criteria. In addition, about "makeup sustainability", a normal life was asked and the state of makeup after 3 hours was evaluated.

“Adhesion to the skin”, “Makeup sustainability”, “No burden on skin”, “Smooth stretch and spread”
(Absolute evaluation criteria)
(Score): (Evaluation)
6: Very good 5: Good 4: Somewhat good 3: Normal 2: Somewhat bad 1: Bad 0: Very bad

(4 step criteria)
(Average score): (Judgment)
More than 5 points: Very good (◎)
Over 3 points and under 5 points: Good (○)
More than 1 point and 3 points or less: Somewhat bad (△)
1 point or less: Defect (x)

“Stability over time” was stored in a constant temperature bath at 40 ° C. for 1 month, and the change in appearance (texture, presence / absence of separation) was evaluated and evaluated according to the following criteria.
(Judgment)
A: No change in appearance.
○: slight change in appearance (slightly bad but no separation)
Δ: Appearance changed to some extent (smooth texture and separation tendency).
X: There is a large change in appearance (separation).

As is apparent from the results in Table 1, the eye color of the present invention has excellent adhesion to the skin and makeup sustainability, has no sense of burden on the skin, has a smooth spread, and has excellent temporal stability. It was a water-in-oil emulsified cosmetic.
On the other hand, Comparative Example 1 using a copolymer that does not contain methacrylic acid as a constituent component of the monomer in place of the siloxy group-containing (meth) acrylic acid copolymer of component (A) is particularly close to the skin. It was inferior in the property, makeup persistence, and temporal stability. Comparative Example 2 using trimethylsiloxysilicic acid in place of component (A) was inferior because it was not satisfactory in terms of adhesion, makeup durability, and burden on skin. Comparative Example 3 in which trimethylsiloxysilicic acid was used instead of component (A) and non-volatile silicone oil was used instead of volatile silicone oil was not satisfactory in terms of adhesion, makeup durability, and stability over time. . Comparative Example 4 using the HLB13 silicone surfactant was not satisfactory in terms of smooth elongation and stability over time.

Example 6: Lipstick (liquid)
(Ingredient) (%)
1. Dextrin palmitate (Note 8) 5
2. Glyceryl tri-2-ethylhexanoate 5
3. Propylene glycol dicaprate 5
4). Decamethylcyclopentasiloxane 30
5. Liquid lanolin 10
6). Siloxy group-containing methacrylic acid copolymer solution 2 20
7). Silicone-based surface activity (HLB = 4.5) (Note 9) 2.5
8). Red number 226 2
9. Yellow iron oxide 0.5
10. Black iron oxide 0.1
11. Silicone-treated iron oxide-coated mica titanium (Note 10) 5
12 Spherical silica powder (average particle size 10 μm) 2
13. Antioxidant (tocopherol acetate) 0.5
14 Preservative (phenoxyethanol) 0.3
15. Purified water remaining amount 16. Ethyl alcohol 3
17. Diglycerin 0.5
18. Locust bean gum 0.1
(Note 8) Leo Pearl KL (Chiba Flour Mills)
(Note 9) Silicon KF-6017 (manufactured by Shin-Etsu Chemical Co., Ltd.)
(Note 10) SA-Timilon Super Kuru Gold (manufactured by Miyoshi Kasei)

(Production method)
A: Components 1 to 3 are heated and dissolved at 90 ° C., then components 4 to 14 are added thereto, and uniformly dispersed with a homomixer.
B: Components 15 to 18 are uniformly dissolved, then added to A and emulsified.
C: After defoaming B, the container was filled into a lipstick.
The lipstick of Example 6 obtained as described above has good adhesion to the lips, excellent makeup sustainability, no sense of burden on the skin, has a smooth spread, and has excellent stability over time. It was a cosmetic.

Example 7: Sunscreen cosmetic (milky liquid)
(Ingredient) (%)
1. 2-methoxyhexyl paramethoxycinnamate 5
2. Siloxy group-containing methacrylic acid copolymer solution 1 30
3. Decamethylcyclopentasiloxane 20
4). Silicone-based surfactant (Note 3) 3
5. Silicone-treated fine particle titanium oxide (Note 11) 5
6). Silicone-treated fine particle zinc oxide (Note 12) 5
7). Organically modified clay mineral (Note 13) 0.5
8). Organically modified clay mineral (Note 14) 0.5
9. Silicone-treated silica (Note 15) 2
10. Purified water remaining amount 11. Ethyl alcohol 5
12 Glycerin 1
13. Xanthan gum 0.1
14 Perfume appropriate amount (Note 11) SI-TTO-S-1 LHC (6%)
(Note 12) SI-UFZO-350 LHC (3%)
(Note 13) Benton 27 (made by Elementis)
(Note 14) Benton 38 (Made by Elementis)
(Note 15) SA-SB-300 (7%)

(Production method)
A: Components 1 to 9 are uniformly dispersed and mixed with a homomixer.
B: Components 10 to 14 are mixed uniformly.
C: A and B were emulsified and filled into a container to obtain a sunscreen cosmetic.
The sunscreen cosmetic of Example 7 obtained as described above is excellent in adhesion to the skin and makeup sustainability (long-lasting sunscreen effect lasts long), has no burden on the skin, and smoothly stretches. The cosmetic was broad and excellent in stability over time.

Example 8: Eyebrow (stick shape)
(Ingredient) (%)
1. Ceresin wax 10
2. Polyethylene wax 3
3. Partially cross-linked organopolysiloxane (Note 16) 1
4). Methylphenylpolysiloxane 3
5. Dimethylpolysiloxane (10 mm ² / s) 2
6). Decamethylcyclopentasiloxane 20
7). Siloxy group-containing methacrylic acid copolymer solution 1 10
8). Silicone-based surfactant (Note 3) 3
9. Silicone surfactant (Note 9) 1
10. Spherical polymethacrylic sanmethyl powder (average diameter 10 μm) 5
11. Silicone-treated mica (Note 17) 5
12 Silicone-treated titanium oxide (Note 5) 1
13. Silicone-treated Bengala (Note 18) 0.3
14 Silicone-treated yellow iron oxide (Note 19) 1
15. Silicone-treated black iron oxide (Note 20) 0.5
16. Smoke-like hydrophobized silica (Note 21) 1
17. Antioxidant (rosemary extract) 0.3
18. Vitamin A oil 0.5
19. Purified water remaining 20.1,3-butylene thiocol 5
21. Alkyl-modified carboxyvinyl polymer (Note 22) 0.3
22. Triethanolamine 0.1
23. Perfume appropriate amount (Note 16) Silicon KSG-15 (manufactured by Shin-Etsu Chemical Co., Ltd.)
(Note 17) SA Excel Mica JP-1 (manufactured by Miyoshi Kasei Co., Ltd.)
(Note 18) SA-Bengara Cloisonne (80%) (manufactured by Miyoshi Kasei)
(Note 19) SA-yellow lemon (80%) (manufactured by Miyoshi Kasei Co., Ltd.)
(Note 20) SA-Black BL-100 (100%) (manufactured by Miyoshi Kasei Co., Ltd.)
(Note 21) CAB-O-SIL TS-530 (Cabot Corporation)
(Note 22) Carbopole 1342 (manufactured by Goodrich)

(Production method)
A: Components 1 to 9 are uniformly dissolved at 100 ° C.
B: Components 10 to 18 are added to A and dispersed uniformly with a despa mixer.
C: Components 19 to 23 are mixed uniformly and brought to 80 ° C.
D: C is added to B, emulsified with a Despera mixer, and defoamed. It was poured into a stick mold at a filling temperature of 80 ° C., cooled and solidified to obtain an eyebrow.
The stick-shaped eyebrow of Example 8 has excellent adhesion to the skin and long-lasting makeup, has no sense of strain on the skin, has a smooth spread, and is stable over time (separated so that the oil oozes out over time). It was also a good cosmetic (without the phenomenon of “sweat” coming).

Example 9: Foundation (liquid)
(Ingredient) (%)
1. Isotridecyl isononanoate 5
2. Di-2-ethylhexanoic acid neopentyl glycol 5
3. Inulin stearate (Note 23) 1
4). Methyl trifluoropropylcyclopolysiloxane 3
5. Decamethylcyclopentasiloxane 20
6). Siloxy group-containing methacrylic acid copolymer solution 2 20
7). Silicone-based surface activity (HLB = 4.5) (Note 24) 3
8). Polyglycerin-modified silicone (HLB = 4.5) (Note 25) 2
9. Organically modified clay mineral (Note 13) 0.5
10. Organically modified clay mineral (Note 14) 0.5
11. Silicone-treated fine particle titanium oxide (Note 11) 5
12 Silicone-treated fine particle zinc oxide (Note 12) 5
13. Silicone-treated mica (Note 17) 3
14 Silicone-treated titanium oxide (Note 5) 5
15. Silicone-treated Bengala (Note 19) 0.3
16. Silicone-treated yellow iron oxide (Note 19) 1.5
17. Silicone-treated black iron oxide (Note 20) 0.2
18. Silicone powder (Note 26) 2
19. Purified water remaining amount 20. Ethyl alcohol 10
21.1,3-butylene glycol 3
22. Xanthan gum 0.1
23. Preservative (phenoxyethanol) 0.3
24. Fragrance 0.2
(Note 23) Leo Pearl ISK (manufactured by Chiba Flour Mills)
(Note 24) KF-6028P (manufactured by Shin-Etsu Chemical Co., Ltd.)
(Note 25) KF-6105 (manufactured by Shin-Etsu Chemical Co., Ltd.)
(Note 26) KSP-100 (manufactured by Shin-Etsu Chemical Co., Ltd.)

(Production method)
A: Components 1 to 3 are dissolved at 90 ° C., then components 4 to 18 are added and uniformly dispersed and mixed with a despa mixer.
B: Components 19 to 24 are mixed uniformly.
C: A and B were emulsified and filled into a container to obtain a foundation.
The foundation of Example 9 obtained as described above has high adhesion to the skin, excellent makeup sustainability, no burden on the skin, smooth extension spread, and excellent stability over time. It was a cosmetic.

Example 10: Cream (ingredient) (%)
1. Decamethylcyclopentasiloxane 20
2. Low viscosity methylpolysiloxane (Note 27) 3
3. Low viscosity methylpolysiloxane (Note 28) 2
4). Silicone surface activity of HLB 10 or less (Note 2) 3
5. Partially cross-linked organopolysiloxane (Note 16) 2
6). Methyl trifluoropropylcyclopolysiloxane 3
7). Siloxy group-containing methacrylic acid copolymer solution 1 10
8). Methyl paraoxybenzoate 0.2
9. Fragrance 0.1
10. Purified water remaining amount 11. Glycerin 1
12 Sodium chloride 1
13.1,3-Butylene glycol 15
14 Marine collagen extract 0.5
(Note 27) KF-96A / 6cs (Shin-Etsu Chemical Co., Ltd.)
(Note 28) KF-96A / 10cs (manufactured by Shin-Etsu Chemical)

(Production method)
A: Components 1 to 7 are uniformly dispersed and mixed with a homomixer.
B: Components 8 to 14 are mixed uniformly.
C: A and B were emulsified and filled into a container to obtain a cream.
The cream of Example 10 obtained as described above has a high adhesion to the skin (strong moist feeling), excellent makeup sustainability (long-term moisturizing persists), and no burden on the skin. It was a cosmetic with a smooth spread and excellent stability over time.

Example 11: Eye color (component) (%)
1. Siloxy group-containing methacrylic acid copolymer solution 3 30
2. Silicone surfactant (Note 3) 3.5
3. Decamethylcyclopentasiloxane 14.5
4). Propylene glycol dicaprate 2
5. Dimethylpolysiloxane (6 mm ² / s) 1
6). Silicone-treated titanium oxide (Note 5) 1
7). Red 226 0.3
8). Bengala 0.2
9. Blue 404 No.0.1
10. Black iron oxide 0.1
11. Silicone-treated talc (Note 6) 2.3
12 Silicone-treated mica titanium (Note 7) 3
13. Spherical nylon powder (average particle size 15 μm) 2
14 Purified water remaining amount 15. Ethyl alcohol 7
16. Glycerin 3
17. Marine collagen extract 0.1
18. Rosemary extract 0.1
19. Preservative (phenoxyethanol) 0.1
20. Fragrance 0.1

(Production method)
A: Components 1 to 13 are mixed uniformly with a homomixer.
B: Components 14 to 20 were uniformly dissolved and mixed, then added to A, emulsified, defoamed, and then filled into a resin container with an applicator to obtain an eye color.
The eye color of Example 11 obtained as described above was excellent in adhesion to the skin and makeup persistence, had no burden on the skin, had a smooth spread, and was excellent in stability over time. It was a water-in-oil emulsified cosmetic.

Claims (3)

The following components (A) to (C);
(A) 55-65 mass% of monomer (a) shown by the following general formula (1)
(In the formula, R ¹ is H or CH ₃ , and p is an integer of 2 to 6)
Monomer (b) represented by the following general formula (2): 20 to 30% by mass
(In the formula, R ² is H or CH ₃ , and R ³ is an alkyl group having 1 to 5 carbon atoms or a phenyl group.)
As a monomer (c), acrylic acid and / or methacrylic acid 15-20 mass%
And a siloxy group-containing (meth) acrylic acid copolymer (B) volatile silicone (C) and a silicone surfactant having a polyoxyethylene chain having an HLB of 10 or less. A water-in-oil emulsified cosmetic.   The water-in-oil emulsified cosmetic according to claim 1, wherein the monomer (b) in the component (A) is methyl methacrylate and the monomer (c) is methacrylic acid.   Further, as component (D), one or more oil gelling agents selected from organically modified clay minerals, fumed hydrophobized silica, dextrin fatty acid esters, and fructooligosaccharide fatty acid esters are blended. 3. A water-in-oil emulsified cosmetic according to 1 or 2.