JP5258394B2 - Cosmetics - Google Patents

Description

  The present invention relates to a cosmetic excellent in feel.

  An oil-in-water emulsified cosmetic with a transparent appearance is produced by using a high-pressure emulsifier, for example, to make a fine emulsion having an average particle size of emulsified particles of 0.2 μm or less (for example, Patent Document 1, Patent Document 2). However, refined emulsions obtained by the high pressure emulsification method generally have a viscosity as low as several tens of mPa · s, and their applications are limited.

A gel-like emulsion having a relatively high viscosity includes a method of thickening a fine emulsion obtained by the above-described high-pressure emulsification method with a water-soluble polymer (Patent Document 3 and the like), an oily component containing solid fat, and water. Is produced by a method (e.g., Patent Document 4) of emulsifying the composition with a hydrophilic surfactant using a high-pressure emulsification method. The cosmetics obtained by these methods have a transparent appearance and have excellent performance, but in terms of usability such as spread, richness and penetration when applied, and touch. There was a need for even better ones.
JP 63-126543 A JP-A-4-48925 JP 2001-342113 A JP 2002-087931 A

  The object of the present invention is a cosmetic that has a high viscosity and a white turbid appearance, has good usability such as spreading, richness and penetration when applied, and excellent feel such as elasticity after application. Is to provide a fee.

  The inventor combined a specific O / W type (oil-in-water type) emulsion with an aqueous solution containing a cationic water-soluble polymer, while having a high-viscosity and cloudy cream-like appearance, It has been found that a cosmetic can be obtained which has good usability such as spreading, richness and penetrating feeling at the time of application, and excellent feel such as elasticity after application.

The present invention includes the following components (A) and (B):
(A) O / W type emulsion containing an oily component containing liquid oil and solid fat as emulsified particles, and the average particle size of the emulsified particles is 0.2 μm or less,
(B) an aqueous solution containing a cationic water-soluble polymer,
Component (A) is a continuous phase, component (B) forms an isolated phase and is phase-separated, viscosity at 25 ° C. is 10000 mPa · s or more, and light transmittance at 550 nm is less than 30% It provides cosmetics that are.

  The cosmetic of the present invention has a high-viscosity and cloudy cream-like appearance, but has good usability such as spreading, richness, and penetrating feeling at the time of application, and excellent feel such as elasticity after application. Is.

  The cosmetic of the present invention contains the components (A) and (B), (C) an oily component containing liquid oil and solid fat as emulsified particles, and the average particle size of the emulsified particles is It is produced by mixing an O / W emulsion having a size of 0.2 μm or less and (D) an aqueous solution containing a cationic water-soluble polymer.

  The fine emulsion (C) and the aqueous solution (D) before mixing are transparent (transmittance of 75% or more), but when the emulsion (C) and the aqueous solution (D) are mixed, the former is a continuous phase. On the other hand, the latter forms an isolated phase, phase-separates and exhibits a cloudy appearance, while maintaining a high viscosity state.

  In a general emulsion having an average particle diameter of 0.2 μm or more, light is scattered by emulsion particle droplets having a size equal to or larger than the wavelength of visible light, and a white turbid appearance is exhibited. However, in the cosmetic of the present invention, the fine average particle size of the emulsified particles is maintained, and the white turbid appearance is formed by coalescence of the emulsified particles obtained by mixing the emulsion (C) and the aqueous solution (D). It is not caused by the large diameter. The cause of the white turbidity of the cosmetic of the present invention is that the particle size corresponding to the island portion of the so-called sea-island type phase separation structure formed by the component (B) is equal to or larger than the wavelength of visible light. Therefore, the light is scattered and a cloudy appearance is exhibited. In general emulsions, the emulsion particles can usually be observed with an optical microscope, but the emulsion particles of the cosmetic of the present invention cannot be observed with an optical microscope. The phase separation state and emulsified particles of the cosmetic of the present invention can be confirmed by observing with an electron microscope. The electron micrograph shows an isolated phase (sea-island type phase-separated structure) consisting of a continuous phase containing fine emulsified particles (sea part of the sea-island type phase-separated structure) and an aqueous solution containing cationic water-soluble polymer. Is observed).

  Usually, the water-soluble polymer is used as a thickener for increasing the viscosity of the cosmetic. However, since the water-soluble polymer is present in the isolated phase in the cosmetic of the present invention, it does not function to increase the viscosity of the cosmetic. Therefore, the high viscosity of the emulsion forming the continuous phase is a factor in the high viscosity of the cosmetic of the present invention. On the other hand, in order to increase the viscosity of cosmetics, generally a large amount of water-soluble polymer is blended. In this case, stickiness and luster due to the water-soluble polymer become problems, but the cosmetic of the present invention does not have such a problem and can give a good feeling of elasticity after application with the water-soluble polymer. As described above, the cosmetic of the present invention has a creamy appearance with high viscosity and white turbidity, but has an internal structure that is clearly different from that of conventional general emulsions, and provides good usability and feel. Inferred.

  In addition, when an emulsion (C) and an aqueous solution (D) are mixed, some movement of water and / or an aqueous medium arises between both. Therefore, component (A) and emulsion (C), component (B) and aqueous solution (D) are not exactly the same. However, the main composition of the component (A) is the same as that of the emulsion (C), and the main composition of the component (B) is the same as that of the aqueous solution (D). Then, the emulsion (C) and aqueous solution (D) as a composition to mix are demonstrated.

The O / W type emulsion (C) contains oily components including liquid oil and solid fat as emulsified particles.
The liquid oil used here is an oily component that is liquid at 25 ° C., for example, hydrocarbon oils such as liquid paraffin, squalane, n-octane, n-heptane, cyclohexane; dioctyl ether, ethylene glycol monolauryl ether, ethylene Ether oils such as glycol dioctyl ether and glycerol monooleyl ether; octyldodecyl myristate, isopropyl palmitate, butyl stearate, myristyl myristate, isopropyl myristate, di-2-ethylhexyl adipate, diisopropyl sebacate, neopentyl dicaprate Ester oil such as glycol and tricaproine; saturated higher alcohol such as isostearyl alcohol and octyldodecanol; unsaturated such as oleyl alcohol and lanolin alcohol Secondary alcohols: Higher fatty acids such as eicosenoic acid, isomyristic acid and capric acid; Higher fatty acid amides such as lauroyl laurylamine and lauric acid butyramide; Fats and oils such as olive oil, soybean oil and cottonseed oil; Dimethylpolysiloxane, cyclic dimethylpolysiloxane, methyl Silicone oils such as phenylpolysiloxane, amino-modified silicone, epoxy-modified silicone, carboxy-modified silicone, alcohol-modified silicone, alkyl-modified silicone, polyether-modified silicone, and fluorine-modified silicone; perfluoroalkylethyl phosphate, perfluoroalkylpolyoxyethylene Fluorine-based oils such as phosphoric acid, perfluoropolyether, polytetrafluoroethylene and the like can be mentioned.

  In particular, liquid paraffin, squalane, isopropyl palmitate, neopentyl glycol dicaprate, ethylene glycol monolauryl ether, perfluoropolyether, and dimethylpolysiloxane are preferred.

Solid fat is a solid or semi-solid (paste-like) oil component at 25 ° C., and examples thereof include aliphatic alcohols, fatty acids, and aliphatic amide derivatives.
As the aliphatic alcohol, a saturated aliphatic alcohol having 12 to 24 carbon atoms such as lauryl alcohol, myristyl alcohol, cetanol, stearyl alcohol, and behenyl alcohol is preferable. The fatty acid is preferably a saturated fatty acid having 12 to 24 carbon atoms such as lauric acid, myristic acid, palmitic acid, stearic acid, and behenic acid. Aliphatic amide derivatives include natural ceramides of type I to type VI, N- (2-hydroxy-3-hexadecyloxypropyl) -N-2-hydroxyethylhexadecanamide, N- (2-hydroxy-3) -Ceramides such as -hexadecyloxypropyl) -N-2-hydroxyethyldecanamide and the like and the like are preferable. Further, sterols such as cholesterol, cholesterol sulfate, polyoxyethylene cholesterol, stigmasterol, ergosterol and the like can also be used.

  One or more oily components can be used, and the emulsion (C) is preferably contained in an amount of 0.1 to 80% by mass (hereinafter simply referred to as%), particularly 1 to 70%.

  In producing the emulsion (C), it is preferable to use a cationic surfactant. Furthermore, in addition to the cationic surfactant, an amphoteric surfactant and a nonionic surfactant of HLB9 or higher can be used. These hydrophilic surfactants preferably have an alkyl or alkenyl group having 10 to 24 carbon atoms, particularly 12 to 18 carbon atoms, as a hydrophobic group.

  Examples of the cationic surfactant include alkyl quaternary ammonium salts such as long chain alkyltrimethylammonium salts and dilong chain alkyldimethylammonium salts, and alkylamine salts. More specifically, for example, lauryl trimethyl ammonium chloride, cetyl trimethyl ammonium chloride, cetyl trimethyl ammonium bromide, stearyl trimethyl ammonium chloride, stearyl trimethyl ammonium bromide, lauryl trimethyl ammonium bromide, dialkyl dimethyl ammonium chloride, dicetyl dimethyl chloride Ammonium, distearyldimethylammonium chloride, dicocoyldimethylammonium chloride, myristyldimethylbenzylammonium chloride, stearyldimethylbenzylammonium chloride, ethyl sulfate lanolin fatty acid aminopropylethyldimethylammonium, ethyl sulfate lanolin fatty acid aminoethyltriethylammonium, ethyl sulfate lanolin fatty acid amino Ethyl diethyl methyl ammonium, Eth Lanolin sulfate fatty acid aminoethyltrimethylammonium sulfate, ethylsulfate lanolin fatty acid aminopropyltriethylammonium, methylsulfate lanolin fatty acidaminoethyltrimethylammonium, methylsulfate lanolin fatty acidaminopropylethyldimethylammonium, ethylsulfate isoalkanoic acid (C14-C20) aminopropylethyldimethylammonium Isoalkanoic acid ethyl sulfate (C18-C22) aminopropylethyldimethylammonium ethylsulfate, aminopropylethyldimethylammonium isostearate, aminopropylethyldimethylammonium isononate, alkyltrimethylammonium saccharin, N- (hexadecyloxyhydroxypropyl) -N-hydroxyethyl hexadecanamide Organic acid salts. Of these, organic acid salts of lauryltrimethylammonium chloride, cetyltrimethylammonium chloride, stearyltrimethylammonium chloride, and N- (hexadecyloxyhydroxypropyl) -N-hydroxyethylhexadecanamide are preferable. Here, organic acids used in the organic acid salt of N- (hexadecyloxyhydroxypropyl) -N-hydroxyethylhexadecanamide include monoacids such as formic acid, acetic acid, propionic acid, butyric acid, isobutyric acid, and valeric acid. Carboxylic acids; Dicarboxylic acids such as succinic acid, phthalic acid, fumaric acid, oxalic acid, malonic acid and glutaric acid; oxycarboxylic acids such as glycolic acid, citric acid, lactic acid, pyruvic acid, malic acid and tartaric acid; glutamic acid and aspartic acid A weak acid whose ionization degree is defined as being significantly smaller than 1 is preferable, and succinic acid, lactic acid, and glutamic acid are preferable.

  Examples of amphoteric surfactants include 2-undecyl-N, N- (hydroxyethylcarboxymethyl) -2-imidazoline sodium, 2-cocoyl-2-imidazolinium hydroxide-1-carboxyethyloxy disodium salt, and the like. Imidazoline-based amphoteric surfactants; 2-heptadecyl-N-carboxymethyl-N-hydroxyethylimidazolinium betaine, lauryldimethylaminoacetic acid betaine, alkylbetaines, amide betaines, sulfobetaines and other betaine-based amphoteric surfactants; N -Amino acid type amphoteric surfactants such as lauroylglycine, N-lauroyl β-alanine, and N-stearoyl β-alanine.

  In order to give a stable emulsification system, the nonionic surfactant is preferably HLB 9 or more, particularly HLB 10 to 17, more preferably HLB 12 to 17. Here, HLB is an index indicating a hydrophilic-lipophilic balance and is defined by the following equation by Oda and Teramura et al.

  Examples of such nonionic surfactants include polyoxyethylene alkyl ether, polyoxyethylene alkenyl ether, polyoxyethylene alkyl phenyl ether, polyoxyethylene hydrogenated castor oil, polyoxyethylene glycerin fatty acid ester, polyoxyethylene sorbitan. Examples include fatty acid esters, polyoxyethylene sorbite fatty acid esters, higher fatty acid sucrose esters, polyglycerin fatty acid esters, polyglycerin alkyl ethers, and alkyl glucoside surfactants.

  Two or more kinds of surfactants may be used, and 0.05 to 30%, particularly 0.05 to 10%, is preferably contained in the emulsion (C).

  Moreover, it is preferable to contain 5 to 99.85% of water in emulsion (C), especially 10 to 98.9%.

Moreover, it is preferable to contain an aqueous solvent in addition to water. As the aqueous solvent, water-soluble alcohols are preferable from the viewpoint of lowering the surface tension of the aqueous phase. Examples of water-soluble alcohols include methyl alcohol, ethyl alcohol, propyl alcohol, isopropyl alcohol, ethylene glycol, propylene glycol, 1,3-butylene glycol, glycerin, sorbitol, mannitol, diethylene glycol, dipropylene glycol, polyethylene glycol (molecular weight: 400 to 20000 ), Sorbitan, sorbitol, maltose, maltotriose and the like.
It is preferable to contain 0.2 to 66%, particularly 1 to 40% of these water-soluble alcohols in the emulsion (C). In addition, water-soluble components such as chelating agents, pH adjusters, preservatives, thickeners, medicinal components, and plant components can be appropriately contained.

  The average particle diameter of the emulsified particles in the emulsion (C) has a size of 0.2 μm or less, for example, 0.01 to 0.2 μm. The average particle size is preferably 0.02 to 0.1 μm. The average particle size is measured by a laser diffraction / scattering method.

Such a finely emulsified O / W type emulsion is, for example, a high-pressure emulsification method, that is, an oily component together with a surfactant and water at a high shearing force, for example, 10 ⁴ s ⁻¹ or more, preferably 10 ⁴ to 10 ^8. It can be produced by emulsification with an emulsifier (for example, a high-pressure homogenizer) capable of obtaining a shear rate of s ⁻¹ , particularly preferably 10 ⁷ to 10 ⁸ s ⁻¹ , or an emulsifier using ultrasonic waves. It can also be produced by utilizing interfacial chemical characteristics such as those prepared by raising the temperature of the system once above the solubilization limit temperature of the system and then cooling it.

When emulsifying with a high-pressure homogenizer, it is preferable to carry out at 10 ⁵ s ^-1 or more, preferably 10 ⁷ to 10 ⁸ s ^-1 at 20 ° C. Such a high shearing force can be obtained by using a high-pressure emulsifier such as a film mix (manufactured by Tokushu Kika Co., Ltd.), a clear mix (manufactured by M Technique Co., Ltd.), a microfluidizer (manufactured by Microfluidics), or DeBEE2000 (BEE (Made by International Co., Ltd.) etc.

For example, a finely emulsified emulsion can be obtained by setting the injection pressure to a range of 300 to 3000 kg / cm ² and a temperature of 5 to 50 ° C. However, the above operating conditions such as pressure and temperature vary depending on the specifications of the apparatus and are not particularly limited. Moreover, the emulsion which has the fine emulsion particle | grains of a desired particle diameter can also be obtained by performing the same high shearing force process to the preliminary | backup emulsion obtained by the normal emulsification method. Moreover, you may perform this high shearing force process repeatedly as needed. Further, an emulsion having a high concentration of the oil component can be produced and then diluted with water or an aqueous medium to obtain an emulsion having a desired concentration.

The emulsion (C) preferably has a viscosity at 25 ° C. of 10,000 mPa · s or more, particularly 20000 to 1000000 mPa · s, in order to ensure the stability of the cosmetic.
In the present invention, the viscosity is measured by using a Brookfield type (B type) rotational viscometer, using rotor Nos. 1 to 4 at 100,000 mPa · s or less, under the measurement conditions of a rotational speed of 6 r / min for 1 minute, At 100,000 mPa · s or higher, a helipath stand is used in combination, and T-shaped bar / spindles No. TA to TE, rotation speed 5 r / min, measurement is performed for 1 minute.

On the other hand, the cationic water-soluble polymer used in the aqueous solution (D) may be either a synthetic polymer or a natural polymer.
Examples of the cationic water-soluble polymer include cationized cellulose, cationic starch, cationized cod gum, cationized guar gum, diallyl quaternary ammonium salt homopolymer, diallyl quaternary ammonium salt / acrylamide copolymer, polyglycol polyamine Condensate, vinyl imidazolium trichloride / vinyl pyrrolidone copolymer, hydroxyethyl cellulose / dimethyl diallylammonium chloride copolymer, vinyl pyrrolidone / quaternized dimethylaminoethyl methacrylate copolymer, vinyl pyrrolidone / alkylamino acrylate copolymer, Vinylpyrrolidone / alkylaminoacrylate / vinylcaprolactam copolymer, vinylpyrrolidone / methacrylamidopropyltrimethylammonium chloride copolymer, alkyl Acrylamide / acrylate / alkylaminoalkylacrylamide / polyethylene glycol methacrylate copolymer, adipic acid / dimethylaminohydroxypropylethylenetriamine copolymer (Cartaretin manufactured by Sandos, USA), JP-A-53-139734, JP-A-60 And cationic polymers described in JP-36407.

The cationic water-soluble polymer preferably has a weight average molecular weight of 10,000 or more, particularly 100,000 to 10,000,000 for the formation of a phase separation structure.
The concentration of the cationic water-soluble polymer contained in the aqueous solution (D) is preferably 0.01 to 10%, particularly 0.05 to 1%, because the feel of the cosmetic is improved.

  The cationic water-soluble polymer is dissolved in water or an aqueous solvent and used as an aqueous solution. Examples of the aqueous solvent include water-soluble alcohols such as methyl alcohol, ethyl alcohol, propyl alcohol, isopropyl alcohol, ethylene glycol, propylene glycol, 1,3-butylene glycol, glycerin, sorbitol, and mannitol. , Diethylene glycol, dipropylene glycol, polyethylene glycol (molecular weight 400 to 10000), sorbitan, sorbitol, maltose, maltotriose and the like, and a mixed solution of these with water may be used.

  In the aqueous solution (D), it is preferable that the aqueous solvent is contained in an amount of 0.01 to 40%, particularly 0.05 to 10% because the feel of the cosmetic is improved. Moreover, it is preferable to contain 99.9-60 mass% of water.

  In addition to the above-mentioned components, it is produced by appropriately containing components used in ordinary cosmetics, such as humectants, powders, fragrances, pigments, ultraviolet absorbers, preservatives, whitening agents, plant extracts and the like.

  The cosmetic of the present invention can be produced by mixing the emulsion (C) and the aqueous solution (D), and the mass ratio when mixing these is (C) :( D) = 60. : 40 to 99: 1, particularly 75:25 to 95: 5, and the ratio of the emulsion (C) is preferably large.

  The composition thus obtained contains an oil component containing component (A) liquid oil and solid fat as emulsified particles, and the O / W type emulsion having an average particle size of the emulsified particles of 0.2 μm or less, In the continuous phase, the aqueous solution containing the component (B) cationic water-soluble polymer forms an isolated phase and is phase-separated. And the external appearance becomes cloudy and the state with a high viscosity is maintained.

  The cosmetic of the present invention has a viscosity at 25 ° C. of 10,000 mPa · s or more, preferably 20000 to 1000000 mPa · s. The viscosity is measured in the same manner as described above.

  The cosmetic of the present invention has a white turbid appearance with a light transmittance of less than 30%, preferably 5% or less at a cell length of 10 mm and 550 nm. The light transmittance is measured with an ultraviolet-visible absorptiometer.

Production Example 1 (Production of emulsion)
Each composition shown in Table 1 was pre-emulsified at 80 ° C. with propeller agitation (200 r / min), and then a high-pressure emulsifier, Microfluidizer (manufactured by Microfluidics) was used, and the injection pressure was 2100 kgf / cm ² The number of times indicated in the item “Pass number” in Table 1 was processed to produce O / W type emulsions C-1 to C-3. In addition, O / W type emulsion C-4 does not perform high-pressure emulsification operation only by preliminary emulsification.
About the obtained O / W type emulsion, the average particle diameter of oil droplets was measured by adjusting a sample by a conventional method using a dynamic light scattering particle size distribution measuring device LB-500 (manufactured by Horiba Seisakusho). . The particle size refers to the arithmetic average diameter. Moreover, the viscosity of the obtained O / W type | mold emulsion was measured at 25 degreeC using the B-type viscosity meter (made by Toki Sangyo). The results are also shown in Table 1.

Production Example 2 (Production of polymer solution)
Polymer solutions D-1 to D-5 having the compositions shown in Table 2 were prepared.
Using a B type (analog type) viscometer manufactured by Toki Sangyo Co., Ltd. or a digital viscometer capable of measuring the same as this, using various types of cylindrical rotors, the viscosity of the resulting polymer solution is determined in a conventional manner Measured at 25 ° C. The results are also shown in Table 2.

Examples 1-12, Comparative Examples 1-12
The emulsion (C) in Table 1 and the solution (D) in Table 2 were mixed at a mass ratio shown in Tables 3 and 4 by propeller stirring (200 r / min) to produce a cosmetic. About the obtained cosmetics, the viscosity in 25 degreeC was measured and the external appearance, the light transmittance, and the phase-separation structure were evaluated. Moreover, the usability at the time of application | coating and the firmness after application | coating were evaluated. The results are shown in Table 3 and Table 4 together.

(Evaluation method)
(1) Viscosity:
Use a B type (analog type) viscometer manufactured by Toki Sangyo or a digital viscometer capable of measuring the same, and if the viscosity is 100,000 mPa · s or less, use various types of cylindrical rotors. Was 100,000 mPa · s or more, various T-shaped spindles and lifting devices were used in combination, and measurement was performed at 25 ° C. by a conventional method.

(2) Appearance:
The appearance of the cosmetic immediately after production was visually observed.

(3) Light transmittance:
The light transmittance at a wavelength of 550 nm (cell length: 10 mm) was measured at 25 ° C. using an ultraviolet-visible absorptiometer UV-160 (manufactured by Shimadzu Corporation).

(4) Phase separation structure:
The presence or absence of a sea-island structure (O / W type emulsion was the sea and the polymer solution was the island) by phase separation was confirmed by electron microscope observation using the freeze fracture method. The case where the sea-island structure by phase separation could be confirmed was indicated as “◯”, and the case where it was not possible was indicated as “X”.

(5) Usability during application and elasticity after application:
10 female panelists use cleansing foams to apply cosmetics to their faces and apply usability (spreading, richness, penetration) when applied, and firmness after application. evaluated. In addition, about the firmness after application | coating, it waited for 3 minutes after completion | finish of application | coating, and judged the firmness of an application part by the feeling when touching a face with a hand. The evaluation was carried out by the following five-stage evaluation, and the average of 10 persons was obtained.
5: Good.
4: Slightly good.
3: Neither.
2: Slightly bad.
1: Bad.

Comparative Example 13
All components of the composition shown in Table 5 (all components corresponding to the composition when 80 parts of the emulsion (C-2) in Table 1 and 20 parts of the solution (D-4) in Table 2 were mixed) After pre-emulsification with propeller stirring (200 r / min), makeup is performed using a high-pressure emulsifier, Microfluidizer (manufactured by Microfluidics Co., Ltd.) under a spraying pressure of 2100 kgf / cm ² for 5 times. The material was manufactured.
About the obtained cosmetics, the viscosity at 25 ° C. is measured in the same manner as in Examples 1 to 12, the appearance, the light transmittance, the phase separation structure are evaluated, and the usability at the time of application and the feeling of elasticity after application are evaluated. evaluated. The results are shown together with 5.

Claims (7)

The following components (A) and (B):
(A) O / W type emulsion containing an oily component containing liquid oil and solid fat as emulsified particles, and the average particle size of the emulsified particles is 0.2 μm or less,
(B) 300,000 average molecular weight selected from cationized cellulose, cationized tara gum, cationized guar gum and N, N-dimethylaminoethyl diethyl methacrylate sulfate / N, N-dimethylacrylamide / polymethacrylate glycol glycol An aqueous solution containing ˜1560,000 cationic water-soluble polymers,
Component (A) is a continuous phase, component (B) forms an isolated phase and is phase-separated, viscosity at 25 ° C. is 10000 mPa · s or more, and light transmittance at 550 nm is less than 30% Cosmetics that are. (C) O / W emulsion containing an oily component containing liquid oil and solid fat as emulsified particles, and the average particle size of the emulsified particles is 0.2 μm or less, and (D) cationized cellulose, cationized Cationic water-soluble high average molecular weight of 300,000 to 1,560,000 selected from cod gum, cationized guar gum and N, N-dimethylaminoethyl diethyl methacrylate methacrylate / N, N-dimethylacrylamide / polymethacrylate glycol dimethacrylate copolymer An aqueous solution containing molecules,
The cosmetic according to claim 1, which is produced by mixing.   The cosmetic according to claim 2, wherein the mass ratio of the emulsion (C) and the solution (D) is (C) :( D) = 60: 40 to 99: 1.   The cosmetic according to claim 2 or 3, wherein the emulsion (C) has a viscosity at 25 ° C of 10,000 mPa · s or more.   The cosmetic according to any one of claims 2 to 4, wherein the emulsion (C) is a fine emulsified O / W emulsion produced by a high-pressure emulsification method.   The emulsion (C) is a fine emulsion O / W emulsion produced by a high-pressure emulsification method from a preliminary emulsion containing water, a cationic surfactant, a liquid oil and a solid fat. Cosmetics given in any 1 paragraph. The cosmetic according to any one of claims 2 to 6, wherein the concentration of the cationic water-soluble polymer contained in the solution (D) is 0.01 to 10% by mass.