JP2021004212A - Emulsion cosmetic - Google Patents

Abstract

To provide an emulsion cosmetic that has low viscosity while enabling skin pores to be corrected.SOLUTION: An emulsion cosmetic composed of an aqueous phase and an oil phase contains (A) silicate, (B) a quaternary ammonium salt type cationic surfactant, and (C) an elastomer, the content of the aqueous phase being 58-70 mass% relative to the total amount of the emulsion cosmetic.SELECTED DRAWING: None

Description

The present invention relates to a low-viscosity emulsified cosmetic capable of correcting pores in the skin.

Conventionally, a water-in-oil emulsified composition having an oil phase as an outer phase and an aqueous phase as an inner phase efficiently applies oil-soluble active ingredients such as emollient oil, oil-soluble chemicals, and ultraviolet absorbers on the skin. It is a formulation suitable for external use on the skin, and is widely used in the cosmetics field for skin care creams, emulsions, hair care creams, and the like.

However, in water-in-oil emulsified cosmetics, the oil constituting the outer phase is gelled, water droplets are immobilized, and the frequency of collision between particles is often reduced to stabilize the oil, which inevitably increases the viscosity. It could be expensive. Therefore, it is said that it is difficult to achieve both low viscosity and stabilization in water-in-oil emulsified cosmetics, and it is difficult to improve stability over time, elongation at the time of application, and good usability at the same time. It was.

As a low-viscosity and stable water-in-oil emulsified cosmetic, for example, Patent Document 1 describes polyoxyethylene hydrogenated castor oil, monoglycerin fatty acid ester or polyglycerin fatty acid ester, branched higher alcohol, and liquid ester oil. W / O type emulsion composition containing the above-mentioned.

Further, Patent Document 2 describes an oil containing an organically modified clay mineral and a hydrophobic silica in a specific amount in a specific amount and further containing a non-polar hydrocarbon oil in a specific ratio, a silicone-based surfactant, and an aqueous phase. A water-in-oil emulsified cosmetic having a low viscosity and excellent stability that can withstand the blending of polar oils by blending the ingredients in a specific amount is described.

Traditionally, many women have longed for clean skin, but there have been no cosmetics that can make bare skin look beautiful, especially cosmetics such as milky lotion, which is a basic cosmetic. In order to make the bare skin look beautiful, it is necessary to add an elastomer that can adjust the texture and correct pores to the cosmetics.

As cosmetics to which an elastomer is added, a water-in-oil emulsified skin external preparation containing an organopolysiloxane elastomer spherical powder, silicone oil, an organically modified clay mineral, and a lipophilic surfactant (Patent Documents). 3 and 4) are mentioned.

JP-A-2018-095588 Japanese Unexamined Patent Publication No. 2014-172853 Japanese Unexamined Patent Publication No. 10-109917 Japanese Unexamined Patent Publication No. 10-109918

The water-in-oil emulsified skin external preparations described in Patent Documents 3 and 4 have a high viscosity because they contain an elastomer, and their properties are creamy or gel-like. For example, when an elastomer is added to a low-viscosity water-in-oil emulsified cosmetic described in Patent Document 2, the viscosity increases and the product becomes creamy. That is, it is difficult to realize a low-viscosity emulsified cosmetic by adding an elastomer effective for correcting skin pores.

The present invention has been made in view of the above problems, and an object of the present invention is to provide an emulsified cosmetic having a low viscosity while being able to correct pores in the skin.

The emulsified cosmetic of the present invention
(A) Silicate and
(B) Quaternary ammonium salt type cationic surfactant,
(C) Elastomer and
An emulsified cosmetic containing an aqueous phase and an oil phase.
The aqueous phase is 58 to 70% by mass based on the total amount of emulsified cosmetics.

The silicate (A) is preferably aluminum magnesium silicate.

(B) The quaternary ammonium salt-type cationic surfactant is preferably disstearyldimethylammonium chloride.

The elastomer (C) is preferably a non-emulsifying silicone elastomer.
The non-emulsifying silicone elastomer is preferably a (dimethicone / phenylvinyldimethicone) crosspolymer.

The content of the elastomer (C) is preferably 0.05 to 1.5% by mass with respect to the total amount of the emulsified cosmetics.

The emulsified cosmetic of the present invention may further contain a silicone surfactant having a (D) HLB value of 8 or less.

The emulsified cosmetic of the present invention preferably has a viscosity of 13000 mPa · s or less.

The emulsified cosmetic of the present invention is preferably a water-in-oil type.

The emulsified cosmetic of the present invention is the emulsified cosmetic of the present invention.
(A) Silicate and
(B) Quaternary ammonium salt type cationic surfactant,
(C) Elastomer and
An emulsified cosmetic containing an aqueous phase and an oil phase.
Since the aqueous phase is 58 to 70% by mass with respect to the total amount of the emulsified cosmetic, it is possible to obtain a low-viscosity emulsified cosmetic while being able to correct the pores of the skin.

Hereinafter, the present invention will be described in detail.
The emulsified cosmetic of the present invention (hereinafter, also simply referred to as cosmetic) is
(A) Silicate and
(B) Quaternary ammonium salt type cationic surfactant,
(C) Elastomer and
An emulsified cosmetic containing an aqueous phase and an oil phase.
The aqueous phase is 58 to 70% by mass based on the total amount of emulsified cosmetics.
Here, (A) silicate is contained in the aqueous phase, (B) a quaternary ammonium salt type cationic surfactant, (C) an elastomer, and (D) a silicone surfactant described later are contained in the oil phase.
Each component will be described in detail.

[Aquatic phase]
(A) Silicate (A) As the silicate, aluminum magnesium silicate, calcium aluminum silicate, sodium aluminum silicate, sodium lithium magnesium silicate, aluminum silicate, magnesium silicate, sodium silicate, silicate. Examples thereof include lithium and calcium silicate, and aluminum magnesium silicate is preferable from the viewpoint of dispersion stability of (A). The aluminum magnesium silicate is more preferably a colloidal hydrous silicate.
These aluminosilicates may be used alone or in combination of two or more.
Examples of commercially available products of aluminum magnesium silicate include "Smecton SA".

In the aqueous phase, in addition to (A) silicate, water (ion-exchanged water, purified water, natural water, etc.) or an aqueous solvent, as well as those that can be usually used for cosmetics, impair the stability of the cosmetics. It can be blended in a range that does not exist.

Typically, lower alcohols, polyhydric alcohols and the like can be blended.
Examples of the lower alcohol include ethanol, methanol, propanol, isopropanol, butanol, isobutanol, t-butanol and the like.
Examples of the polyhydric alcohol include divalent alcohols (eg, ethylene glycol, propylene glycol, trimethylene glycol, 1,2-butylene glycol, 1,3-butylene glycol, tetramethylene glycol, 2,3-butylene glycol, and the like. Pentamethylene glycol, 2-butene-1,4-diol, hexylene glycol, octylene glycol, etc.; trivalent alcohol (eg, glycerin, trimethylolpropane, etc.); tetravalent alcohol (eg, 1,2,6) -Pentaerythritol such as hexanetriol); pentavalent alcohol (eg, xylitol, etc.); hexavalent alcohol (eg, sorbitol, mannitol, etc.); polyhydric alcohol polymer (eg, diethylene glycol, dipropylene glycol, triethylene glycol, etc.) , Polypropylene glycol, tetraethylene glycol, diglycerin, polyethylene glycol, triglycerin, tetraglycerin, polyglycerin, etc.; divalent alcohol alkyl ethers (eg, ethylene glycol monomethyl ether, ethylene glycol monoethyl ether, ethylene glycol monobutyl ether) , Ethylene glycol monophenyl ether (phenoxyethanol), ethylene glycol monohexyl ether, ethylene glycol mono2-methylhexyl ether, ethylene glycol isoamyl ether, ethylene glycol benzyl ether, ethylene glycol isopropyl ether, ethylene glycol dimethyl ether, ethylene glycol diethyl ether, ethylene Glycoldibutyl ether, etc.); Dihydric alcohol alkyl ethers (eg, diethylene glycol monomethyl ether, diethylene glycol monoethyl ether, diethylene glycol monobutyl ether, diethylene glycol dimethyl ether, diethylene glycol diethyl ether, diethylene glycol butyl ether, diethylene glycol methyl ethyl ether, triethylene glycol monomethyl ether, tri) Ethylene glycol monoethyl ether, propylene glycol monomethyl ether, propylene glycol monoethyl ether, propylene glycol monobutyl ether, propylene glycol isopropyl ether, dipropylene glycol methyl ether, dipropylene glycol ethyl A Tel, dipropylene glycol butyl ether, etc.); dihydric alcohol ether esters (eg, ethylene glycol monomethyl ether acetate, ethylene glycol monoethyl ether acetate, ethylene glycol monobutyl ether acetate, ethylene glycol monophenyl ether acetate, ethylene glycol diazibate, ethylene Glycerol dissuccinate, diethylene glycol monoethyl ether acetate, diethylene glycol monobutyl ether acetate, propylene glycol monomethyl ether acetate, propylene glycol monoethyl ether acetate, propylene glycol monopropyl ether acetate, propylene glycol monophenyl ether acetate, etc.); glycerin monoalkyl ether ( For example, xyl alcohol, ceracyl alcohol, batyl alcohol, etc.); Sugar alcohol (eg, sorbitol, martitol, maltotriose, mannitol, sucrose, erythritol, glucose, fructose, starch-degrading sugar, maltose, xylitol, starch-degrading, etc. (Reduced alcohol, etc.); Glysolid; Tetrahydrofurfuryl alcohol; POE-tetrahydrofurfuryl alcohol, POP-butyl ether; POP / POE-butyl ether; Tripolyoxypropylene glycerin ether; POP-glycerin ether; POP-glycerin ether phosphoric acid; Examples thereof include POP / POE-pentaneerythritol ether and polyglycerin.

In the present invention, the blending amount of the aqueous phase with respect to the total amount of the emulsified cosmetic is 58 to 70% by mass. When the blending amount of the aqueous phase is 58% by mass or more, the viscosity can be made low, and the usability can be made good, and when it is 70% by mass or less, it is sufficiently stable. You can get sex. The blending amount of the aqueous phase with respect to the total amount of the emulsified cosmetic is preferably 59 to 68% by mass, more preferably 60 to 66% by mass.

[Oil phase]
(B) Quaternary ammonium salt type cationic surfactant
As the quaternary ammonium salt-type cationic surfactant, disstearyldimethylammonium chloride is preferably mentioned from the viewpoint of emulsion stability (storage stability). Other quaternary ammonium salt-type cationic surfactants include, for example, dodecyltrimethylammonium chloride, myristyltrimethylammonium chloride, cetyltrimethylammonium chloride, stearyltrimethylammonium chloride, araquiltrimethylammonium chloride, behenyltrimethylammonium chloride, and myristyldimethyl. Ethylammonium chloride, cetyldimethylethylammonium chloride, stearyldimethylethylammonium chloride, araquildimethylethylammonium chloride, behenyldimethylethylammonium chloride, myristyldiethylammonium chloride, cetyldiethylmethylammonium chloride, stearyldiethylmethylammonium chloride, araquildiethyl Methylammonium chloride, behenyldiethylmethylammonium chloride, benzyldimethylmyristylammonium chloride, benzyldimethylcetylammonium chloride, benzyldimethylstearylammonium chloride, benzyldimethylbehenylammonium chloride, besylmethylethylcetylammonium chloride, benzylmethylethylstearylammonium chloride, di Examples thereof include behenyldihydroxyethylammonium chloride and the equivalent bromide, as well as dipalmitylpropyl ethylammonium methyl sulfate and the like.
These quaternary ammonium salt-type cationic surfactants may be used alone or in combination of two or more.

(C) Elastomer The (C) elastomer is preferably a silicone elastomer, and examples thereof include a silicone elastomer (organopolysiloxane). The silicone elastomer includes, for example, a crosslinked silicone (crosslinked organopolysiloxane) in which a silicone polymer is three-dimensionally crosslinked. The silicone elastomer is more preferably a non-emulsifying silicone elastomer. The non-emulsifying silicone elastomer refers to a silicone elastomer whose crosslinked portion or main chain is not modified with a polyoxyalkylene group. In particular, the non-emulsifying silicone elastomer is preferably composed of a hydrophobic portion (does not have a hydrophilic portion). When an emulsified silicone elastomer having a polyoxyalkylene group is added, stickiness like a surfactant is generated, and the smoothness when applying the cosmetic to the skin tends to be lost. On the other hand, when a non-emulsifying silicone elastomer is used, it is possible to suppress stickiness and obtain smoothness (smoothness) when applied to the skin.

Examples of silicone elastomers include dimethicone crosspolymer, (dimethicone / vinyl dimethicone) crosspolymer, (dimethicone / phenylvinyldimethicone) crosspolymer, (vinyldimethicone / lauryldimethicone) crosspolymer, (laurylpolydimethylsiloxyethyl dimethicone / bis- Examples thereof include vinyl dimethicone) crosspolymer, alkyl (C30-45) cetearyl dimethicone crosspolymer, and cetearyl dimethicone crosspolymer. Of these, a (dimethicone / phenylvinyldimethicone) crosspolymer is more preferable from the viewpoint of non-cohesiveness of the silicone elastomer and correction of skin pores.

As the elastomer, for example, a commercially available product can be used. The commercially available product may be a mixture of a silicone elastomer and an oily component. The oily component contained in this commercially available product is not particularly limited as long as it is applicable to the skin. For example, examples of commercially available products containing silicone elastomers include KSG-18A, KSG-16, KSG-15AP (all manufactured by Shinetsu Silicone Co., Ltd.), and elastomer blend DC9045 (manufactured by Toray Dow Corning Co., Ltd.).

The content of the elastomer is preferably 0.05 to 1.5% by mass, more preferably 0.2 to 1.2% by mass, and further 0.5 to 0.5% by mass with respect to the total amount of the emulsified cosmetic. It is desirable that it is 1.0% by mass. When the content of the silicone elastomer is 0.05% by mass or more with respect to the total amount of the emulsified cosmetic, a higher pore correction effect can be obtained. Further, when the content of the silicone elastomer is 1.5% by mass or less with respect to the total amount of the emulsified cosmetic, the silicone elastomer can be dispersed more stably.

(D) Silicone surfactant having an HLB value of 8 or less In the cosmetic of the present invention, a silicone surfactant having an HLB (Hydrophile-Lipohile Balance) value of 8 or less calculated by using the Griffin method is further used for the oil phase. It may be included. The silicone surfactant is preferably a polyether-modified silicone surfactant. As the polyether-modified silicone surfactant, for example, a polyether-modified silicone in which a polyoxyalkylene group such as polyoxyethylene (POE) or polyoxypropylene (POP) is introduced into the silicone skeleton can be used. Of these, it is particularly preferable that the silicone surfactant has a silicone chain (siloxane chain) as a main chain and a hydrophilic group having a polyether group as a side chain. It is more preferable that the silicone surfactant has a pendant type (comb type) structure in which a plurality of polyoxyalkylene groups (polyether chains) are introduced into the silicone chain as side chains. When the silicone surfactant has a pendant type structure, the dispersion stability of the silicone elastomer can be further enhanced.

As the silicone surfactant having an HLB value of 8 or less, for example, a polyoxyethylene methylpolysiloxane copolymer, a cetyldimethicone copolyol, or the like can be used. Examples of commercially available polyoxyethylene methyl polysiloxane copolymers include polyethylene glycol (PEG) -3 dimethicone (silicone KF-6015, Shinetsu Chemical Industry Co., Ltd.) and PEG-9 methyl ether dimethicone (silicone KF-6016, Shinetsu). Chemical Industry Co., Ltd.), PEG-10 dimethicone (silicone 6015, KF-6017, KF-6017P, KF-6043, Shinetsu Chemical Industry Co., Ltd.), cetyl PEG / PPG10 / 1 dimethicone (silicone KF-6048, Shinetsu Chemical Industry Co., Ltd.), etc. Can be mentioned.

The content of the silicone surfactant is preferably 0.3 to 5% by mass, more preferably 0.5 to 4% by mass, and 0.8 to 3% by mass with respect to the total amount of the emulsified cosmetic. And more preferable. When the content of the silicone surfactant is 0.3% by mass or more, the dispersibility of the silicone elastomer can be further ensured. Further, when the content of the silicone surfactant is 5% by mass or less, the emulsification stability can be further improved.

(Other oil phase components)
The oil phase of the emulsified cosmetic of the present invention is not particularly limited as long as it is an oily component that can be usually blended in cosmetics. For example, silicone oil, synthetic ester oil, hydrocarbon oil, higher fatty acid, higher alcohol. , Oils and fats, waxes and the like.

Examples of the silicone oil include chain polysiloxanes such as dimethylpolysiloxane, methylphenylpolysiloxane, and methylhydrogenpolysiloxane; cyclic polysiloxanes such as decamethylpolysiloxane, dodecamethylpolysiloxane, and tetramethyltetrahydrogenpolysiloxane; 3 Examples thereof include silicone resin and silicone rubber forming a dimensional network structure.

Synthetic ester oils include isopropyl myristate, cetyl octanoate, octyldodecyl myristate, isopropyl palmitate, butyl stearate, hexyl laurate, myristyl myristate, decyl oleate, hexyldecyl dimethyloctanoate, cetyl lactate, myristyl lactate. , Lanolin acetate, Isocetyl stearate, Isocetyl isostearate, Cholesteryl 12-hydroxystearyl, Ethylene glycol di-2-ethylhexylate, Dipentaerythritol fatty acid ester, N-alkylglycol monoisostearate, Neopentyl glycol dicaprate, Appleic acid Diisostearyl, glycerin di-2-heptylundecanoate, trimethylolpropane tri-2-ethylhexylate, trimethylolpropane triisostearate, pentanerythritol tetra-2-ethylhexylate, glycerin tri-2-ethylhexylate, triisostearate Methylolpropane, cetyl 2-ethylhexanoate, 2-ethylhexyl palmitate, glycerin trimyristate, glyceride tri-2-heptylundecanoate, methyl ester of castor oil fatty acid, oleic acid oil, acetoglyceride, 2-heptylun palmitate Decyl, diisobutyl adipate, N-lauroyl-L-glutamic acid-2-octyldodecyl ester, di-2-heptylundecyl adipate, ethyllaurate, di-2-ethylhexyl sebatate, 2-hexyldecyl myristate, palmitin Examples thereof include 2-hexyldecyl acid, 2-hexyldecyl adipate, diisopropyl sebatate, 2-ethylhexyl succinate, ethyl acetate, butyl acetate, amyl acetate, triethyl citrate, and crotamitone (C ₁₃ H ₁₇ NO).

Examples of the hydrocarbon oil include liquid paraffin, ozokerite, squalene, pristane, paraffin, ceresin, squalene, petrolatum, microcrystalline wax and the like.

Higher fatty acids include lauric acid, myristic acid, palmitic acid, stearic acid, behenic (behenic acid) acid, oleic acid, 12-hydroxystearic acid, undecylenic acid, tollic acid, isostearic acid, linoleic acid, linoleic acid, and eicosapentaenoic acid. (EPA), docosahexaenoic acid (DHA) and the like are exemplified.

Higher alcohols include linear alcohols such as lauryl alcohol, cetyl alcohol, stearyl alcohol, behenyl alcohol, myristyl alcohol, oleyl alcohol, and cetostearyl alcohol; monostearyl glycerin ether (bacyl alcohol), 2-decyltetradecinol, lanolin alcohol, etc. Examples thereof include branched alcohols such as cholesterol, phytosterol, hexyldodecanol, isostearyl alcohol, and octyldodecanol.

Fats and oils include avocado oil, camellia oil, evening primrose oil, turtle oil, macadamia nut oil, corn oil, mink oil, olive oil, rapeseed oil, egg yolk oil, sesame oil, persic oil, wheat germ oil, southern ka oil, castor oil, and flaxseed oil. , Saflower oil, cotton seed oil, eno oil, soybean oil, peanut oil, tea seed oil, kaya oil, rice bran oil, cinnamon oil, Japanese coconut oil, jojoba oil, germ oil, triglycerin, glycerin trioctanoate, triisopalmitic acid Liquid fats and oils such as glycerin; cacao butter, coconut oil, horse fat, hardened coconut oil, palm oil, beef fat, sheep fat, hardened beef fat, palm kernel oil, pork fat, beef bone fat, mokuro kernel oil, hardened oil, cow legs Examples thereof include solid fats and oils such as fats, mokuro, and hardened coconut oil.

Examples of waxes include honey wax, candelilla wax, cotton wax, carnauba wax, baby wax, squid wax, whale wax, montan wax, nukarou, lanolin, capoc wax, lanolin acetate, liquid lanolin, sugar cane, lanolin fatty acid isopropyl, hexyl laurate, reduced lanolin, jojo Examples thereof include barrow, hard lanolin, cellac wax, POE lanolin alcohol ether, POE lanolin alcohol acetate, POE cholesterol ether, lanolin fatty acid polyethylene glycol, and POE hydrogenated lanolin alcohol ether.

Further, the emulsified cosmetic of the present invention preferably has a viscosity of 13000 mPa · s or less, more preferably 2500 to 12000 mPa · s, and further preferably 3000 to 11000 mPa · s. When the viscosity is 13000 mPa · s or less, the elongation at the time of application is light and a good usability can be obtained. On the other hand, when it is 2500 mPa · s or more, sufficient stability can be obtained. The viscosity of the emulsified cosmetic of the present invention is the viscosity measured under the conditions shown in Examples.

The emulsified cosmetic of the present invention is preferably a water-in-oil type because the components (A) to (C) can be efficiently spread on the skin.

The emulsified cosmetic of the present invention includes other optional additive components usually used in cosmetics as long as the effects of the present invention are not impaired, such as surfactants, metal ion sequestering agents, powder components, sugars, amino acids, and organic substances. Amines, pH adjusters, UV absorbers, skin nutrients, vitamins, antioxidants, antioxidants, fragrances and the like can be appropriately added as needed.

The emulsified cosmetic of the present invention can be prepared by a conventional method, and the emulsifying method is not particularly limited. For example, the aqueous phase and the oil phase are each heated to about 70 ° C., the heated aqueous phase is gradually added to the oil phase, emulsified by an emulsifier, and then allowed to cool to room temperature. However, it is not limited to this.

The emulsified cosmetic of the present invention can be widely applied to cosmetics. For example, in addition to emulsions, products such as sun care cosmetics (sunscreen, sun oil, after-sun lotion, etc.), makeup bases, emulsified foundations, etc. Can be mentioned.

Hereinafter, the present invention will be described in more detail with reference to Examples, but the present invention is not limited to these Examples. In addition, the blending amount in the following examples and the like shows mass% unless otherwise specified.
Cosmetics were prepared by a conventional method according to the formulations listed in Tables 1 and 2 below. The physical characteristics (viscosity, emulsified particle size) of the prepared cosmetics were measured as follows. In addition, storage stability and pore correction were evaluated as follows.

(viscosity)
The viscosity of the cosmetic was measured at 30 ° C. with a BL type viscometer (manufactured by VS-A type Shibaura System) under rotor No. 3, 12 rpm, and 1 minute measurement conditions.

(Emulsified particle size)
The particle size of the emulsified particles in the cosmetics of Examples and Comparative Examples was measured using ZETASIZER (registered trademark) Nano ZS90 (manufactured by Malvern).

(Storage stability)
After storing the prepared cosmetics in a constant temperature bath at 50 ° C., the condition was observed and evaluated according to the following criteria.
A: No change after 1 month B: Creamed after 1 month C: Creamed after 2 weeks D: Creamed immediately after preparation

(Pore correction effect)
Five panels conducted an actual use test in which the cosmetics of Examples and Comparative Examples were applied to the face, and evaluated according to the following criteria.
A: 4 to 5 people who felt the correction effect after application B: 1 to 3 people who felt the correction effect after application C: 0 people who felt the correction effect after application Table 1 with the evaluation results And 2 show.

As shown in Table 1, Examples 1 to 4 in which the amount of the aqueous phase blended with respect to the total amount of the emulsified cosmetics was 58 to 70% by mass had good storage stability and a sufficient pore correction effect. On the other hand, Comparative Example 1 did not become a milky lotion, and Comparative Example 2 did not have sufficient storage stability.
Further, as shown in Table 2, Comparative Example 3 containing no elastomer does not have sufficient storage stability and pore correction effect, contains a large amount of elastomer, and contains 57 aqueous phases with respect to the total amount of emulsified cosmetics. In Comparative Example 4 by mass%, the dosage form could not be cream. On the other hand, in Examples 2 and 5 in which the content of the silicone elastomer was in the range of 0.05 to 1.5 mass with respect to the total amount of the emulsified cosmetic, a high pore correction effect was obtained while maintaining the storage stability. ..

Claims (9)

(A) Silicate and
(B) Quaternary ammonium salt type cationic surfactant,
(C) Elastomer and
An emulsified cosmetic containing an aqueous phase and an oil phase.
An emulsified cosmetic having an aqueous phase of 58 to 70% by mass based on the total amount of the emulsified cosmetic. The emulsified cosmetic according to claim 1, wherein the silicate (A) is magnesium aluminum silicate. The emulsified cosmetic according to claim 1 or 2, wherein the (B) quaternary ammonium salt-type cationic surfactant is distearyldimethylammonium chloride. The emulsified cosmetic according to claim 1, 2 or 3, wherein the (C) elastomer is a non-emulsifying silicone elastomer. The emulsified cosmetic according to claim 4, wherein the non-emulsifying silicone elastomer is a (dimethicone / phenylvinyldimethicone) crosspolymer. The emulsified cosmetic according to any one of claims 1 to 5, wherein the content of the elastomer (C) is 0.05 to 1.5% by mass with respect to the total amount of the emulsified cosmetic. (D) The emulsified cosmetic according to any one of claims 1 to 6, further comprising a silicone surfactant having an HLB value of 8 or less. The emulsified cosmetic according to any one of claims 1 to 7, which has a viscosity of 13000 mPa · s or less. The emulsified cosmetic according to any one of claims 1 to 8, which is a water-in-oil type.