JP2008120732A - Emulsified cosmetic - Google Patents

Abstract

<P>PROBLEM TO BE SOLVED: To provide an easily coatable emulsified cosmetic having good stability with time, and excellent skin care effects and slimming effects. <P>SOLUTION: The emulsified cosmetic contains (A) a polyether-modified silicone, (B) an oil solution, (C) a water-soluble polymer thickener, (D) Hemerocallis citrina or an extract thereof and (E) water. <P>COPYRIGHT: (C)2008,JPO&INPIT

Description

  The present invention relates to an emulsified cosmetic excellent in skin care effect and slimming effect.

  Obesity is a result of excessive intake energy relative to energy consumed, which accumulates as neutral fat in white fat cells. Obesity with a large accumulation of visceral fat has been pointed out to be related to pathological conditions such as insulin resistance and arteriosclerosis, and obesity with a large accumulation of subcutaneous fat is large regardless of gender from the viewpoint of beauty. It is a problem.

Conventionally, in order to reduce excess fat on the face and body and maintain a firm body, in addition to various exercises and dietary restrictions, cosmetics such as massage gels and creams that promote metabolism in the body have been used. . For such cosmetics, caffeine, a plant extract having a lipolysis-promoting action (Patent Document 1), and the like are used for the purpose of promoting the decomposition of fat and obtaining a slimming effect.
However, none of them has a sufficient effect, and a cosmetic having a more slimming effect has been desired.

In addition, since such cosmetics are applied and used over a wide range of the body, there is no need for dripping or the like, easy to take in the hands, easy to apply to the skin, and easy to massage.
Japanese Patent Laid-Open No. 2005-60366

  An object of the present invention is to provide a cosmetic that is easy to apply and excellent in skin care effect and slimming effect.

  By using a combination of a polyether-modified silicone, an oil agent and a water-soluble polymer thickener and a specific plant or an extract thereof, the present inventors have good stability over time, easy application, and skin care effects. And it discovered that the emulsified cosmetics excellent in the slimming effect were obtained, and completed this invention.

The present invention includes the following components (A), (B), (C), (D) and (E):
(A) polyether-modified silicone,
(B) oil agent,
(C) a water-soluble polymer thickener,
(D) Yellow flower vegetables or an extract thereof,
(E) An emulsified cosmetic containing water is provided.

  The emulsified cosmetic of the present invention has good stability over time, good spread, easy application to the skin, and excellent skin care and slimming effects.

  Examples of the polyether-modified silicone of component (A) used in the present invention include those represented by the following general formulas (1) to (3).

[Wherein R ¹ represents an alkyl group having 1 to 5 carbon atoms or a phenyl group, and R ² represents the formula — (CH ₂ ) _r —O— (C ₂ H ₄ O) _s — (C ₃ H ₆ O) _t— R ⁵ (R ⁵ is a hydrogen atom or an alkyl group having 1 to 5 carbon atoms, r is a number of 1 to 5, s is a number of 1 to 50, and t is a number of 0 to 30). , R ³ and R ⁴ represent the same group as any one of R ¹ or R ² , p represents a number of 5 to 300, and q represents a number of 1 to 50. However, not all of R ¹ are phenyl groups.

[Wherein R ¹ , R ² , p and q represent the same meaning as described above, R ⁶ represents an alkyl group having 2 to 20 carbon atoms, and R ⁷ and R ⁸ represent R ¹ , R ² or R ⁶ . The same group as any one is shown, and u shows the number of 1-30. However, not all of R ¹ are phenyl groups.

[Wherein R ⁹ represents an alkyl group having 1 to 4 carbon atoms, and R ¹⁰ represents the formula —Q ¹ —O— (C ₂ H ₄ O) _x — (C ₃ H ₆ O) _y R ¹⁴ (Q ¹ Is a hydrocarbon group having 1 to 4 carbon atoms, R ¹⁴ is a hydrogen atom, an alkyl group or acetyl group having 1 to 4 carbon atoms, x is an integer of 1 or more, and y is an integer of 0 or more. R ¹¹ represents a group represented by the formula —Q ² —OR ¹⁵ (Q ² is a hydrocarbon group having 1 to 4 carbon atoms, R ¹⁵ is a hydrocarbon group having 8 to 30 carbon atoms), and R ¹² and R ¹³ are R ⁹ , R ¹⁰ or R ¹¹ represents the same group, α is an integer of 0 or more, β and γ are integers of 1 or more.

  The polyether-modified silicones represented by the general formulas (1) to (3) have a branched structure in the silicone main chain or are co-modified with a functional group other than the polyether without departing from the purpose. May be.

  Examples of the compound represented by the general formula (1) include KF-6017 (manufactured by Shin-Etsu Chemical Co., Ltd.), SH-3772C (manufactured by Toray Dow Corning), and the like. The compound represented by the general formula (2) is referred to as alkyl polyether-modified silicone, and examples thereof include KF-6038 (manufactured by Shin-Etsu Chemical Co., Ltd.), Avil WE-09 (manufactured by Goldschmidt), and the like. The compound represented by the general formula (3) is a polyoxyalkylene alkyl ether co-modified organopolysiloxane, which is easily produced by, for example, co-modifying methyl hydrogen polysiloxane with polyoxyalkylene allyl ether and allyl alkyl ether. be able to.

In addition, as the component (A), a partially crosslinked polyether-modified silicone can be used. Such partially crosslinked polyether-modified silicone is obtained by addition polymerization of an organohydrogenpolysiloxane and an aliphatic unsaturated group-containing compound, and is described in JP-A-4-72932, JP-A-5-40320, and the like. What is done is illustrated. The partially crosslinked polyether-modified organopolysiloxane polymer has the following general formula (4):
R ¹⁶ _a R ¹⁷ _b H _c SiO _{(4-abc) / 2} (4)

[Wherein R ¹⁶ represents an alkyl group, aryl group, aralkyl group or halogenated hydrocarbon group which may have a substituent having 1 to 18 carbon atoms, and R ¹⁷ represents a formula —C _n H _2n O ( C ₂ H ₄ O) _d (C ₃ H ₆ O) _e R ¹⁸ (R ¹⁸ is a hydrogen atom, a saturated aliphatic hydrocarbon group having 1 to 10 carbon atoms, or —C (O) —R ¹⁹ (R ¹⁹ is carbon D represents an integer of 2 to 200, e is an integer of 0 to 200, d + e is an integer of 3 to 200, and n is an integer of 2 to 6, respectively. A) represents 1 ≦ a ≦ 2.5, b represents 0.001 ≦ b ≦ 1, and c represents 0.001 ≦ c ≦ 1.
And / or general formula (5)
R ¹⁶ _f H _g SiO _{(4-fg) / 2} (5)

[Wherein R ¹⁶ represents the same meaning as described above, f represents 1.0 ≦ f ≦ 3.0, and g represents 0.001 ≦ g ≦ 1.5, respectively]
An organohydrogenpolysiloxane represented by the general formula (a)
C _m H _2m-1 O (C ₂ H ₄ O) _h (C ₃ H ₆ O) _i C _m H _2m-1 (a)

[Wherein, h is an integer of 2 to 200, i is an integer of 0 to 200, h + i is an integer of 3 to 200, and m is 2 to 6]
And / or the general formula (b)
R ¹⁶ _j R ²⁰ _k SiO _{(4-jk) / 2} (b)

[Wherein R ¹⁶ represents the same meaning as described above, R ²⁰ represents a C 2-10 monovalent hydrocarbon group having an aliphatic unsaturated group at its terminal, j is 1 ≦ j ≦ 3, k is 0.001 ≦ k ≦ 1.5 respectively]
In the combination with the organopolysiloxane represented by the formula (4) and / or a polymer having the component represented by the general formula (a) as an essential raw material.

  As the component (A), an alkyl polyether-modified silicone is particularly preferable, and a partially crosslinked alkyl polyether-modified silicone is particularly preferable because of its superior stability over time and applicability to the skin.

  One or more kinds of the polyether-modified silicone as the component (A) can be used, and 0.5 to 15% by mass, particularly 1 to 10% by mass in the total composition is preferable for stability over time and to the skin. It is preferable because it is more excellent in coating properties.

The oil agent of component (B) used in the present invention is not particularly limited as long as it is used in ordinary emulsified cosmetics. For example, hydrocarbon oils, animal and vegetable oils, ester oils, higher fatty acids, higher alcohols, silicone oils. , Phospholipids, sphingosine derivatives and the like.
Of these, hydrocarbon oils such as liquid paraffin and squalane; silicone oils such as dimethylpolysiloxane are preferred.

  One or more kinds of the oil agent of component (B) can be used, and it is preferable to contain 0.5 to 20% by mass in the whole composition because of excellent skin care effect, and particularly 2 to 10% by mass. It is preferable because the stability over time is more excellent.

  The water-soluble polymer thickener of component (C) used in the present invention is not particularly limited as long as it is used in ordinary emulsified cosmetics. For example, vinyl polymers, cellulose polymers, xanthan gum, Carrageenan, gelatin, hyaluronic acid, tuberose polysaccharide and the like.

  Examples of the vinyl polymer include carboxyvinyl polymer, alkyl acrylate copolymer, acrylic acid / alkyl methacrylate copolymer, polyacrylic acid, polyvinyl alcohol, polyvinyl pyrrolidone, and salts thereof.

  Among these, as the acrylic acid-based (co) polymer, for example, carbopol (Noveon), synthalene (3Vsigma), PEMULEN (Noveon) and the like can be used.

  Examples of the cellulose polymer include methyl cellulose, hydroxyethyl cellulose, hydroxyethyl methyl cellulose, hydroxypropyl cellulose, hydroxypropyl methyl cellulose, carboxymethyl cellulose sodium, methyl hydroxypropyl cellulose, and the like.

Further, as the component (C), a cationic cross-linked copolymer can be used, and at least one of a cationic group-containing vinyl monomer (hereinafter referred to as monomer (c ₁ )) and an amide group-containing vinyl. At least one monomer (hereinafter referred to as monomer (c ₂ )) and at least a cross-linkable vinyl monomer (hereinafter referred to as monomer (c ₃ )) having two or more vinyl groups in the molecule. A cationic cross-linked copolymer obtained by radical polymerization of one kind can be suitably used.

As the monomer (c ₁ ), (meth) acrylic acid esters or (meth) acrylamides having a dialkylamino group, styrenes having a dialkylamino group, vinylpyridines, N-vinyl heterocyclic compounds, amino groups And a monomeric acid neutralized product or a quaternary ammonium salt, a diallyl-type quaternary ammonium salt, and the like.
Among these, dimethylaminoethyl (meth) acrylate, diethylaminoethyl (meth) acrylate, dimethylaminopropyl (meth) acrylamide, quaternary ammonium salt quaternized with quaternizing agent of diethylaminopropyl (meth) acrylamide, or dimethyl Diallylammonium chloride and the like are preferable.

  Examples of the acid for obtaining the acid neutralized product include hydrochloric acid, sulfuric acid, acetic acid, citric acid, succinic acid, adipic acid, sulfamic acid, and the like. Preferred quaternizing agents for obtaining a quaternary ammonium salt Examples thereof include alkyl halides such as methyl chloride and methyl iodide, diethyl sulfate, and di-n-propyl sulfate.

As the monomer (c ₂ ), the general formula (6) or (7)

(Wherein R ²¹ represents a hydrogen atom or a methyl group, and R ²² and R ²³ are the same or different and each represents a hydrogen atom or a linear or branched alkyl group or alkenyl group having 1 to 4 carbon atoms, R ²² and R ²³ together represent — (CH ₂ ) _n — (n is an integer of 3 to 6) or — (CH ₂ ) ₂ —O— (CH ₂ ) ₂ —, and the adjacent nitrogen atom is Forming a ring containing)

(Wherein R ²¹ represents the same meaning as described above, and A ¹ represents — (CH ₂ ) _m — (m represents an integer of 2 to 5)).
The monomer represented by these is mentioned.

  Specifically, N-methyl (meth) acrylamide, N, N-dimethyl (meth) acrylamide, N, N-diethyl (meth) acrylamide, Nn-propyl (meth) acrylamide, Nt-butylacrylamide, N- (meth) acryloylmorpholine, N-vinyl piperidone, N-vinyl pyrrolidone and the like can be mentioned. Among these, a feeling of use is preferable when N, N-disubstituted acrylamide is used, and N, N-dimethyl (meth) acrylamide, N, N-diethyl (meth) acrylamide and the like are more preferable.

Examples of the monomer (c ₃ ) include (meth) acrylic acid esters of polyhydric alcohols or unsaturated alcohols, acrylamides, divinyl compounds, polyallyl compounds, and the like. Of these, ethylene glycol di (meth) acrylate, polyethylene glycol di (meth) acrylate, pentaerythritol tetra (meth) acrylate, allyl etherified pentaerythritol, vinyl (meth) acrylate, allyl (meth) acrylate, and the like are preferable. .

A preferable blending ratio of the monomer (c ₁ ) and the monomer (c ₂ ) is 2/98 to 98/2, more preferably 3 in terms of a molar ratio of (c ₁ ) / (c ₂ ). / 97 to 60/40. It is preferable for the molar ratio to be within this range, since both the properties of thixotropy and the retention of viscosity at a low share rate are adequately exhibited. When the blending ratio of the monomer (c ₁ ) is excessive from the range shown here, the tendency to lack thixotropic properties. Moreover, when the blending ratio of the monomer (c ₂ ) is excessive from the range shown here, the viscosity at the low shear rate tends to be low.

The ratio of the monomer (c ₃ ) is preferably 0.0002 to 2 in terms of molar ratio with respect to the total amount of monomers, particularly preferably 0.0002 to 1, and more preferably 0.0002 to 0.4. When the ratio of the monomer (c ₃ ) is within the above range, the hydrogel formed from the resulting copolymer has a sufficient viscosity, and the hydrogel feels soft and slippery.

  The cationic cross-linked copolymer may contain other vinyl monomers copolymerizable with one or more of the above-mentioned three types of vinyl monomers as essential constituent units. it can. Examples of other vinyl monomers include (meth) acrylic acid alkyl esters such as methyl (meth) acrylate and ethyl (meth) acrylate; anionic group-containing monomers such as acrylic acid and methacrylic acid; N- ( And betaines such as 3-sulfopropyl) -N-acryloyloxyethyl-N, N-dimethylammonium betaine and N-carboxymethyl-N-methacryloyloxyethyl-N, N-dimethylammonium betaine.

  Such a cationic cross-linked copolymer can be produced, for example, according to the method described in JP-A-2005-170800.

  One or more polymer thickeners of component (C) can be used, and 0.05 to 3% by mass, particularly 0.1 to 2% by mass in the total composition is applied to the skin. It is preferable because of its good properties and excellent temporal stability.

  Ingredients (D) yellow rape are Helicocarpus licorice (Hemerocallis plicata Stepf (Chugakudai Dictionary, edited by Shanghai Science and Technology Publishers and Shogakukan, Volume 1, Shogakukan Co., Ltd., 1985, p114)), Honkanzo (Hemerocallis fulva L. (Chokuyaku Daiten Dictionary, edited by Shanghai Science and Technology Publishers and Shogakukan, Volume 1, Shogakukan Co., Ltd., 1985, p378)), Yabukanzo (Hemerocalis fulva L. Technical Publishing Company and Shogakukan, Vol. 1, Shogakukan Co., Ltd., 1985, p381, p539)), Hemeralis flava L. (Chokuyaku Daiten Dictionary, Shanghai Science and Technology Publishing Company and Shogakukan, Vol. 1) , Shogakukan Co., Ltd., 1985, p378, p539 )), Hemerocallis minor Mill. (Chukayaku Dictionary, edited by Shanghai Science and Technology Publishers and Shogakukan, Volume 1, Shogakukan Co., Ltd., 1985, p378, p539)) and related plants A generic term for plant flowers and buds.

  In the present invention, “yellow flower vegetables” includes all of these series of plants. It is preferable to use the yellow rape vegetables that are distributed in the market as they are or dried (also known as gold needle vegetables). In addition, drying can apply the method normally used for drying of a plant, for example, any of a sun, a wind, a heating, or freeze-drying may be sufficient.

  As the yellow flower vegetable extract used in the present invention, the above-mentioned "yellow flower vegetable" is extracted at room temperature or under heating, and a solvent extract obtained by preparing it, a diluted solution thereof, a concentrated solution thereof or a dried product thereof. Can be mentioned.

  In the present invention, examples of the method for extracting yellow flower vegetables extract include immersion, decoction, leaching, reflux extraction, supercritical extraction, ultrasonic extraction, and microwave extraction.

  As the extraction solvent used for extracting the yellow flower vegetable extract, either a polar solvent or a nonpolar solvent can be used, and these can be used in combination.

  Examples of polar solvents include water, alcohols, ketones, and nonpolar solvents such as esters, chain and cyclic ethers, polyethers, hydrocarbons, aromatic hydrocarbons, pyridines, Examples include critical carbon dioxide, fats and oils, waxes, and other oils.

  Examples of alcohols include methanol, ethanol, propanol, butanol, propylene glycol, butylene glycol and the like. Examples of ketones include acetone and methyl ethyl ketone. Examples of the esters include methyl acetate and ethyl acetate. Examples of chain and cyclic ethers include tetrahydrofuran and diethyl ether. Examples of polyethers include polyethylene glycol. Examples of hydrocarbons include hexane, cyclohexane, petroleum ether, and the like. Examples of aromatic hydrocarbons include benzene and toluene.

  Among these, it is preferable to use water or an alcohol alone or a water-alcohol mixture, more preferably a water-alcohol mixture, and particularly preferably a water-methanol or water-ethanol mixture. In the case of a water-alcohol mixture, the mixing ratio (V / V) of alcohol to the mixture is preferably 0 to 80%, more preferably 0 to 60%.

  Although the usage-amount of an extraction solvent changes also with the kind of solvent, Preferably it is 1-100 mass parts with respect to 1 mass part of dried yellow vegetables, More preferably, it is 5-20 mass parts.

  Moreover, extraction temperature is 5-70 degreeC, Preferably it is 5-50 degreeC, More preferably, it is 10-40 degreeC. The extraction time is 1 hour to 30 days, preferably 7 to 14 days.

  The yellow rape extract can be used after extraction / preparation as a liquid or diluted, but the extract liquid is concentrated under reduced pressure, freeze concentrated or membrane concentrated, wind, heated or lyophilized, concentrated, It may be prepared and used in a paste or dry product (powder).

  Moreover, it is preferable to use what the inactive impurities removed from the said yellow flower vegetable extract by well-known techniques, such as liquid-liquid distribution, solid-liquid distribution, a filtration membrane, activated carbon, adsorption resin, an ion exchange resin. Furthermore, you may use, after performing processes, such as a deodorizing and a decoloring, as needed.

  The component (D) yellow rape or extract thereof is contained in the total composition in an amount of 0.005 to 5% by mass, particularly 0.05 to 2% by mass in terms of dry matter, to maintain the effect of the present invention. However, it is preferable because it is more stable.

  The component (E) water used in the present invention imparts product applicability, moderate refreshment and stability, and is contained in the total composition in an amount of 57 to 98 mass%, particularly 76 to 96 mass%. preferable.

  The emulsified cosmetic of the present invention can further contain (F) an oil gelling agent, and can further improve the temporal stability. Examples of the oil gelling agent include fatty acid dextrins such as dextrin palmitate, dextrin myristate, and dextrin stearate, and dextrin palmitate is particularly preferable.

  The oil gelling agent of component (F) is preferably contained in the total composition in an amount of 0.01 to 1% by mass because it is excellent in feeling of use and stability, and particularly 0.1 to 0.4% by mass. Is preferable because it is more excellent in use feeling and stability.

  The emulsified cosmetic of the present invention can further contain (G) caffeine or a salt thereof, and can further enhance the skin care effect and the slimming effect.

  As caffeine or a salt thereof, a commercially available one may be used, but it is extracted from a plant having a high caffeine content such as coffee beans, green tea leaves, oolong tea, black tea and mate tea by the above or a known extraction method, It may be a plant extract or a synthetic product obtained by preparation. Moreover, you may use the said plant or its extract as a caffeine supply source. The caffeine may be a dry product, a liquid or a paste.

  Examples of caffeine salts include mineral acid salts such as hydrochloric acid and sulfuric acid, and organic acid salts such as acetic acid and citric acid.

  Component (G) caffeine or a salt thereof is contained in the total composition in an amount of 0.01 to 2% by mass, particularly 0.05 to 0.5% by mass, while maintaining the effects of the present invention. It is preferable because of its superiority.

The emulsified cosmetic of the present invention can further contain (H) menthol, and can feel a squeaky feeling.
Menthol is preferably contained in the whole composition in an amount of 0.005 to 1% by mass from the viewpoint that a feeling of squeezing can be felt, and in particular, 0.05 to 0.3% by mass of menthol is squeezed and refreshing. This is preferable because it is more stable.

  In addition to the above components, the emulsified cosmetic of the present invention is a component used in ordinary emulsified cosmetics, such as preservatives, ultraviolet absorbers, antioxidants, sequestering agents, dyes, inorganic pigments, and polymer powders. , Perfume and the like.

The emulsified cosmetic of the present invention can be produced by a usual method.
The emulsified cosmetic of the present invention is particularly preferably in the form of a milk or cream having a viscosity at 25 ° C. of 10,000 to 100,000 mPa · s.

Production Example 1 (Manufacture of yellow flower vegetable extract)
400 g of 50% (v / v) ethanol-water mixed solution was added to 40 g of yellow flower vegetables (Shinwa Bussan Co., Ltd.), extracted for 7 days at room temperature (20-30 ° C.), and then filtered to obtain 340 mL of an extract. The solvent was distilled off from this extract under reduced pressure to obtain 18.4 g of a dried product.

Examples 1-14, Comparative Examples 1-4
Emulsified cosmetics having the compositions shown in Tables 1 and 2 were produced and evaluated for stability over time, applicability to the skin, skin care effect and skin tightening effect. The results are shown in Table 1 and Table 2 together. In addition, the commercially available caffeine (Wako Pure Chemical Industries Ltd.) was used.

(Production method)
A polyether-modified silicone and an oil agent are dispersed at room temperature, further heated, and mixed by stirring to prepare an oil phase. When an oil gelling agent is added, it is added to the heated oil phase. The aqueous phase obtained by dispersing the water-soluble polymer thickener in purified water is sufficiently stirred while being slowly added to the oil phase. After uniformly emulsifying, it is cooled and other ingredients are added at room temperature. At this time, when caffeine and / or menthol are contained, these are also added. Furthermore, a yellow flower vegetable extract solution was added and mixed to obtain an emulsified cosmetic.

(Evaluation methods)
(1) Stability over time:
After each emulsified cosmetic was stored at 50 ° C. for 30 days, its appearance was visually evaluated according to the following criteria.
3: No change is observed, uniform and stable.
2: Some change is recognized.
1: Changes such as separation are observed.

(2) Applicability to skin:
Three special panels evaluated each of the emulsified cosmetics comprehensively for ease of stretching and ease of massaging when a certain amount was applied to the inner side of the forearm, and judged in the following five stages. The results are shown as average values.
5: Very good.
4: Good.
3: Neither can be said.
2: Slightly bad.
1: Bad.

(3) Skin care effect:
Emulsified cosmetic material 0.2 g is uniformly applied in a circle having a diameter of 3 cm on the inner side of the forearm, washed with water and dried 1 hour after the application. The skin conductance after washing and drying was measured with a Corneometer CM825PC (COLOGNE). From the amount of change from the skin conductance before the treatment (Δ skin conductance), the skin care effect was evaluated according to the following criteria. The larger this value, the higher the skin care effect.
4: The skin conductance value is extremely increased (Δ skin conductance ≧ 15).
3: Increased skin conductance value (15> Δ skin conductance ≧ 5).
2: Skin conductance value slightly increased (5> Δ skin conductance ≧ 2).
1: Skin conductance value does not change (2> Δ skin conductance).

(4) Skin tightening effect:
The emphasis effect when each emulsified cosmetic was applied to the calf for 1 month was comprehensively evaluated by 5 specialist panels, and judged according to the following 4 levels. The results are shown as average values.
4: A strong effect is strongly felt.
3: Feels the squeezing effect.
2: Feels a slight effect.
1: There was no squeezing effect.

Example 15
An emulsified cosmetic having the following composition was produced. About the obtained emulsified cosmetics, it carried out similarly to Examples 1-14, and time-dependent stability, the applicability | paintability to skin, a skin care effect, and the skin tightening effect were evaluated. As a result, the stability over time: 3, the application property to the skin: 4.7, the skin care effect: 4, and the skin tightening effect: 3.6.

(composition)
(1) Crosslinked alkyl polyether-modified silicone (KSG310, manufactured by Shin-Etsu Silicone) 5.0 (mass%)
(2) Cross-linked methylpolysiloxane (KSG15, manufactured by Shin-Etsu Silicone) 2.0
(3) Silicone (10cs) 3.0
(4) Liquid paraffin 4.0
(5) Polyglyceryl monoisostearate (Cosmol 41V, manufactured by Nisshin Oilio Co., Ltd.) 0.5
(6) Ethanol 3.0
(7) Menthol 0.1
(8) Dextrin palmitate 0.1
(9) Cationic crosslinked polymer (Sofcare KG-301P, manufactured by Kao Corporation) 0.4
(10) Yellow Flower Vegetable Extract (Production Example 1) 0.5
(11) Caffeine 0.2
(12) Methylparaben 0.2
(13) Purified water balance (14) Perfume appropriate amount

(Production method)
The aqueous phase in which the component (9) is dispersed in the component (13) is added to the oil phase in which the components (1) to (5) and (8) are dispersed at room temperature and further heated and mixed with stirring. To do. After uniformly emulsifying, cool and add components (6), (7) and (12) mixed at room temperature, and add and mix components (10), (11) and (14) Thus, an emulsified cosmetic was obtained.

Claims (4)

The following components (A), (B), (C), (D) and (E):
(A) polyether-modified silicone,
(B) oil agent,
(C) a water-soluble polymer thickener,
(D) Yellow flower vegetables or an extract thereof,
(E) An emulsified cosmetic containing water.   The emulsified cosmetic according to claim 1, further comprising (F) an oil gelling agent.   The emulsified cosmetic according to claim 1 or 2, further comprising (G) caffeine or a salt thereof.   The emulsified cosmetic according to any one of claims 1 to 3, further comprising (H) menthol.