Slurry dispersion, cosmetic, and method for producing the same
The use of a slurry-like dispersion with trimethylsiloxysilicic acid, hydrophobically treated pigments, and a liquid oil agent in cosmetics addresses the issue of pigment dispersibility and color unevenness, resulting in improved stability and aesthetic properties.
Patent Information
- Application Number
- JP2022561911
- Authority / Receiving Office
- JP · JP
- Patent Type
- Patents
- Current Assignee / Owner
- Priority Date
- 2020-11-13
- Filing Date
- 2021-11-08
- Publication Date
- 2025-06-03
- Estimated Expiration
- 2041-11-08
AI Technical Summary
Existing cosmetics face challenges with pigment dispersibility, leading to color unevenness and reduced aesthetic properties, while increasing surfactant levels can compromise usability.
A slurry-like dispersion containing trimethylsiloxysilicic acid or its derivatives, hydrophobically treated colored pigments, and an oil agent liquid at 25°C, which improves pigment dispersibility and adhesion without compromising usability.
The solution enhances pigment dispersibility, preventing color unevenness and improving the temporal stability and aesthetic properties of cosmetics, while maintaining a light touch and good spreadability.
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Abstract
Description
Technical Field
[0001] The present invention relates to a slurry dispersion, a cosmetic, and a method for producing the same, which contain trimethylsiloxysilicic acid.
Background Art
[0002] Generally, in cosmetics, trimethylsiloxysilicic acid is used as a film-forming agent and is blended for the purpose of improving the makeup retention of cosmetics. Patent Document 1 discloses trimethylsiloxysilicic acid having a modified group such as a polyether group, a polyglycerin group, or silicone. However, although research has been conducted on the makeup retention effect such as oil resistance, no research has been conducted on the dispersibility of coloring pigments.
[0003] On the other hand, Patent Document 2 discloses a technique for improving the finish after application by blending trimethylsiloxysilicic acid in makeup cosmetics (Patent Document 2). However, the trimethylsiloxysilicic acid used here is for the purpose of improving the finish after application, and no research has been conducted on improving the color separation or dispersibility of coloring pigments. In makeup cosmetics such as foundation, usability, spreadability, and adhesion when applied to the skin are required, while high aesthetic properties such as no color separation or color unevenness are also desired.
Prior Art Documents
Patent Documents
[0004]
Patent Document 1
Patent Document 2
Summary of the Invention
Problems to be Solved by the Invention
[0005] The present invention has been made in view of the above circumstances, and by being incorporated into cosmetics, it has a good feel (light touch), good spreadability (elongation), excellent adhesion, and improved pigment dispersibility, thereby suppressing color unevenness. An object of the present invention is to provide a slurry-like dispersion, a cosmetic containing the same, and a method for producing the same.
Means for Solving the Problems
[0006] In cosmetics that are formulated with pigments for coloring, the pigments aggregate, and color separation phenomena such as sedimentation and separation occur, deteriorating the temporal stability of the cosmetics, losing aesthetic properties, and reducing the commercial value, which can be a problem in some cases. Also, if the amount of surfactants or the like is increased to prevent pigment aggregation and improve dispersibility, problems may occur in terms of usability, such as a heavy and sticky feel, and it is difficult to simultaneously satisfy usability and dispersibility. Such phenomena are particularly prominent in emulsion-type cosmetics such as cream foundations and liquid foundations, which are base makeup. In addition, in these base makeup products, compared to point makeup, the application area is wider, so furthermore, spreadability such as good elongation and the adhesion of the cosmetics to the skin are also emphasized.
[0007] As a result of intensive studies to achieve the above object, the present inventors have found that the above problems can be solved by using a slurry-like dispersion containing (A) one or more selected from trimethylsiloxysilicic acid and its derivatives, (B) a hydrophobically treated colored pigment, and (C) an oil agent that is liquid at 25°C, and have thus arrived at the present invention.
[0008] Therefore, the present invention provides the following inventions. 1. A slurry-like dispersion containing (A) one or more selected from trimethylsiloxysilicic acid and its derivatives, (B) a hydrophobically treated colored pigment, and (C) an oil agent that is liquid at 25°C 2. The slurry dispersion according to claim 1, wherein the content of component (A) is 0.1 to 10% by mass, the content of component (B) is 20 to 89.9% by mass, and the content of component (C) is 10 to 40% by mass. 3. The slurry dispersion according to claim 1 or 2, wherein component (C) is an oil agent selected from hydrocarbons and esters that are liquid at 25°C. 4. The slurry dispersion according to any one of claims 1 to 3, wherein the mass ratio (A) / (B) of component (A) to component (B) is 0.005 to 0.05. 5. A cosmetic containing 1 to 30% by mass of the slurry dispersion according to any one of claims 1 to 4. 6. The cosmetic according to claim 5, wherein the cosmetic is a water-in-oil emulsion cosmetic and contains 1.5% by mass or less of (D) an organically modified clay mineral. 7. The cosmetic according to claim 6, wherein the content of component (D) is 0.1 to 0.8% by mass in the whole cosmetic. 8. Step (I) of preparing a slurry dispersion by mixing one or more selected from (A) trimethylsiloxysilicic acid and its derivatives, (B) a hydrophobically treated coloring pigment, and (C) an oil agent that is liquid at 25°C, mixing the obtained slurry dispersion with an oil phase component, and mixing an aqueous phase component with the obtained mixture II-1, or mixing an oil phase component and an aqueous phase component, and mixing the slurry dispersion with the obtained mixture II-2 A method for producing a water-in-oil emulsion cosmetic having the above steps.
Advantages of the Invention
[0009] The present invention can provide a slurry dispersion that, when formulated in a cosmetic, has a good usability (light touch), good spreadability (elongation), excellent adhesion, and improved pigment dispersibility, thereby suppressing color unevenness, a cosmetic containing the same, and a method for producing the same.
Embodiments for Carrying Out the Invention
[0010] The present invention will be described in detail below. In the present invention, the names of ingredients may be described in cosmetic labeling names or International Nomenclature of Cosmetic Ingredients (INCI).
[0011] I. Slurry-like Dispersion The slurry dispersion of the present invention is a slurry dispersion containing (A) one or more members selected from trimethylsiloxysilicate and its derivatives, (B) a hydrophobically treated color pigment, and (C) an oil agent that is liquid at 25°C.
[0012] [Component (A)] Component (A) of the present invention is one or more selected from trimethylsiloxysilicate and its derivatives, and may be used alone or in combination of two or more. Component (A) improves the dispersibility of the hydrophobically treated color pigment of component (B) in the cosmetic preparation and inhibits color separation, thereby preventing deterioration of the stability over time of the cosmetic preparation and loss of aesthetics.
[0013] Trimethylsiloxysilicate (INCI) is not limited to any compound used in ordinary cosmetics. It is a compound with a crosslinked structure with a siloxane structure as the main skeleton, and has the average composition formula [(CH 3 ) 3 SiO 1 / 2 ] a [SiO 2 ] b (wherein a is 1 to 3, and b is 0.5 to 8) is preferable. 3 ) 3 SiO 1 / 2 ] a (CH 3 Derivatives of trimethylsiloxysilicate in which a portion of the silsesquioxane is substituted with polyoxyalkyl ether, glycerin, or dimethylpolysiloxane can be used. When a derivative of trimethylsiloxysilicate is used, the dispersibility may be good, but the feeling of use may be heavy. When a good feeling of use (lightness) is desired, trimethylsiloxysilicate is preferred.
[0014] The weight average molecular weight of component (A) is preferably from 1,000 to 20,000, more preferably from 1,000 to 10,000, and still more preferably from 1,000 to 3,000, for the purpose of improving the dispersibility of the pigment. In the present invention, the weight average molecular weight is a value determined by GPC (gel permeation chromatography) analysis using polystyrene as a standard substance under the following conditions. [Measurement conditions] Developing solvent: Tetrahydrofuran (THF) Flow rate: 0.6 mL / min Detector: Differential refractive index detector (RI) Column: TSK Guardcolumn SuperH-H TSKgel SuperHM-N (6.0 mm I.D. × 15 cm × 1) TSKgel SuperH2500 (6.0 mm I.D. × 15 cm × 1) (All are manufactured by Tosoh Corporation) Column temperature: 40°C Sample injection volume: 50 μL (THF solution with a concentration of 0.3 mass%)
[0015] The property of component (A) may be liquid, gum-like, paste-like, solid, etc. at 25°C, but liquid is preferred from the viewpoint of the effect of improving color unevenness. Further, component (A) may be used in the form of a solution or dispersion diluted with a solvent from the viewpoint of handling during compounding. As the solvent for dilution, one or more selected from dimethylpolysiloxane, decamethylcyclopentasiloxane, and isododecane are preferred. As commercially available products, KF-7312J (a mixture solution of 50% by mass of decamethylcyclopentasiloxane + 50% by mass of trimethylsiloxysilicic acid), KF-7312K (a mixture solution of 40% by mass of dimethicone (6cs) + 60% by mass of trimethylsiloxysilicic acid), KF-9021 (a mixture solution of 50% by mass of decamethylcyclopentasiloxane + 50% by mass of trimethylsiloxysilicic acid), X-21-5249 (a mixture solution of 50% of decamethylcyclopentasiloxane + 50% of trimethylsiloxysilicic acid), X-21-5595 (a mixture of 40% by mass of isododecane + 60% by mass of trimethylsiloxysilicic acid), etc. (all manufactured by Shin-Etsu Chemical Co., Ltd.) can be used. Specific examples of the liquid include X-21-5250 (a mixture solution of 50% of decamethylcyclopentasiloxane + 50% of trimethylsiloxysilicic acid), X-21-5250L (a mixture solution of 50% by mass of dimethicone (6cs) + 50% by mass of trimethylsiloxysilicic acid), X-21-5616 (a mixture solution of 50% by mass of isododecane + 50% by mass of trimethylsiloxysilicic acid), etc.
[0016] In the present invention, component (A) avoids the aggregation of the hydrophobized coloring pigment and suppresses color separation, but in addition to component (A), when a dispersant or emulsifier generally used in cosmetics, that is, a silicone-modified acrylic polymer, an alkyl polyether-modified silicone, etc. is used alone, the effect may not be exhibited. Since component (A) of the present invention has little influence on emulsification, it is preferably used in both oil-in-water type cosmetics and water-in-oil type cosmetics, but oil-in-water type cosmetics are preferred in terms of adhesion.
[0017] The content of component (A) is preferably 0.1 to 10% by mass, more preferably 0.5 to 5% by mass, and even more preferably 0.8 to 2.5% by mass in the slurry-like dispersion. If it is less than 0.1% by mass, sufficient dispersibility may not be obtained, and if it exceeds 10% by mass, the viscosity of the slurry-like dispersion may increase.
[0018] [Component (B)] Component (B) of the present invention is a hydrophobized coloring pigment and can be used alone or in combination of two or more. The coloring pigment of the hydrophobized coloring pigment according to the present invention is not particularly limited as long as it is a pigment usually used for coloring cosmetics, and includes iron oxide red, iron oxide yellow, titanium oxide white, iron oxide black, red lead, red ocher, yellow ocher, manganese violet, cobalt violet, chromium hydroxide, chromium oxide, cobalt oxide, cobalt titanate, iron oxide-doped titanium oxide, iron titanate, (titanium / titanium oxide) fired product, (Li / cobalt) titanate, cobalt titanate, titanium nitride, iron hydroxide, inorganic brown pigments such as γ-iron oxide, inorganic yellow pigments such as loess, lake pigments obtained by lake-forming tar-based dyes, lake pigments obtained by lake-forming natural pigments, and other colored pigments. Any of them can be used.
[0019] In addition, the shape of the pigment according to the present invention may be any shape such as spherical, substantially spherical, rod-shaped, spindle-shaped, petal-shaped, strip-shaped, irregular-shaped, etc., and there is no particular limitation on its geometric aspect as long as it can impart color to cosmetics. Also, from the viewpoint of hiding power, a pigment having a particle diameter, that is, an average particle diameter in the range of 150 to 600 nm is preferable. The average particle diameter in the present invention refers to a value obtained by analyzing an image taken by TEM (transmission electron microscope) based on the number. If it is less than 150 nm, the hiding power is low, so the coloring efficiency of the cosmetics may be reduced, and if it is larger than 600 nm, the usability may deteriorate.
[0020] Furthermore, the pigment according to the present invention may be partially or entirely surface-treated with an inorganic compound such as alumina, aluminum hydroxide, silica, or hydrous silica.
[0021] The hydrophobic treatment refers to subjecting the coloring pigment to a surface treatment with a hydrophobic treatment agent. The surface hydrophobic treatment agent for the coloring pigment according to the present invention is not particularly limited as long as it can impart hydrophobicity, and examples thereof include silicone treatment agents, waxes, paraffins, organic fluorine compounds such as perfluoroalkyl and phosphates, surfactants, amino acids such as N-acylglutamic acid, and metal soaps such as aluminum stearate and magnesium myristate. A silicone treatment agent is preferred.
[0022] Examples of the silicone treatment agent include silanes or silylating agents such as caprylyl silane (manufactured by Shin-Etsu Chemical Co., Ltd.: AES-3083) and trimethoxysilyl dimethicone, silicones such as dimethyl silicone (manufactured by Shin-Etsu Chemical Co., Ltd.: KF-96A series), methyl hydrogen type polysiloxane (manufactured by Shin-Etsu Chemical Co., Ltd.: KF-99P, KF-9901, etc.), silicone branched type silicone treatment agents (manufactured by Shin-Etsu Chemical Co., Ltd.: KF-9908, KF-9909, etc.), and silicone compounds such as acrylic silicone (manufactured by Shin-Etsu Chemical Co., Ltd.: KP-574, KP-541). Among them, the silicone powder treatment agent described in Japanese Patent No. 3912961 is preferably used, and triethoxysilyl ethyl polydimethylsiloxyethyl hexyl dimethicone, which is a dimethyl polysiloxane having a triethoxysilyl group, a polydimethylsiloxyethyl group, and a hexyl group in the side chain (manufactured by Shin-Etsu Chemical Co., Ltd.: KF-9909), etc., can be effectively used from the viewpoint of exhibiting high affinity even when the dispersion medium for dispersing the highly hydrophobic treated coloring pigment according to the present invention has a mixed composition such as silicone and hydrocarbon. Further, the above surface hydrophobic treatment agent can be used alone or in combination of two or more.
[0023] In the present invention, the method of surface-treating a coloring pigment with a hydrophobizing agent is not particularly limited and can be carried out by known methods. The surface treatment method can be broadly classified into a dry method and a wet method. As the dry method, for example, any stirrer, grinder, mixer, disperser, etc., such as a Henschel mixer, ball mill, jet mill, kneader, planetary mixer, sand mill, attritor, ribbon blender, disperser mixer, homomixer, etc., can be used to mix / contact the coloring pigment used in the present invention with the hydrophobizing agent for treatment. At this time, treatment may be carried out while applying energy such as heating, mechanochemical mechanical force, and superheated steam. Further, after sufficiently mixing or contacting the coloring pigment and the hydrophobizing agent, energy such as heating, mechanochemical mechanical force, and superheated steam may be separately applied for treatment. Or when mixing or contacting the hydrophobizing agent with the coloring pigment, for the purpose of improving the dispersion efficiency of the hydrophobizing agent, the hydrophobizing agent may be previously dissolved or dispersed in an arbitrary amount of water, solvent or supercritical fluid, and means such as spraying this on the coloring pigment may be used. As the wet method, it is possible to disperse, mix or contact the coloring pigment and the hydrophobizing agent in water, solvent or supercritical fluid, then evaporate the solvent, and further apply energy such as heating, mechanochemical mechanical force or superheated steam for treatment.
[0024] Specific examples of the colored pigment subjected to the hydrophobized surface treatment include the KTP-09 series, particularly KTP-09W, 09R, 09Y, 09B, etc. (manufactured by Shin-Etsu Chemical Co., Ltd.).
[0025] The content of the component (B) is preferably 20 to 89.9% by mass, more preferably 30 to 85% by mass, and even more preferably 70 to 85% by mass in the slurry-like dispersion. If it is less than 20% by mass, the coloring power may be insufficient, and if it exceeds 90% by mass, the aggregation of the coloring pigments may become strong.
[0026] In the slurry-like dispersion, the mass ratio (A) / (B) of component (A) to component (B) is preferably from 0.005 to 0.05, more preferably from 0.01 to 0.03. By setting the above range to 0.005 to 0.05, the dispersion effect of component (A) on component (B) can be obtained more effectively.
[0027] [Component (C)] Component (C) is an oil agent that is liquid at 25°C and can be used alone or in combination of two or more. The oil agent that is liquid at 25°C is not particularly limited as long as it is used in ordinary cosmetics. For example, vegetable oils such as jojoba oil and olive oil, animal oils such as liquid lanolin, linear or branched hydrocarbons such as liquid paraffin, light isoparaffin, fluid isoparaffin, squalane, and squalene, esters such as alcohol fatty acid esters and polyhydric alcohol fatty acid esters, and silicones such as dimethylpolysiloxane, dimethylcyclopolysiloxane, and methylphenylpolysiloxane can be used.
[0028] Among these, low-viscosity hydrocarbons, silicones, esters, etc. are preferred. More specifically, as the hydrocarbon, isododecane, dodecane, liquid paraffin, squalane, (C13-15) alkane are preferred, and as the ester, isotridecyl isononanoate, isononyl isononanoate, ethylhexyl palmitate, triethylhexanoin, cetyl ethylhexanoate, hexyl laurate, glyceryl tri(caprylate / caprate) are preferred. As the silicone, dimethylpolysiloxane, decamethylcyclopentasiloxane, diphenylsiloxyphenyltrimethicone, methyltrimethicone, etc. with a viscosity of 50 mm 2 / s or less at 25°C are preferred.
[0029] The content of component (C) is preferably 10 to 40% by mass, more preferably 15 to 35% by mass, and even more preferably 15 to 25% by mass in the slurry-like dispersion. If it is less than 10% by mass, there is a risk that wetting to component (B) may be insufficient, and if it exceeds 40% by mass, there is a risk that the fibrillation force may be insufficient. In particular, when dispersing with a three-roll mill, 15 to 30% by mass is preferable, and 15 to 25% by mass is even more preferable.
[0030] In addition, the oily agent that is liquid at 25 °C and used as component (C), for the purpose of adjusting the feel of use and imparting emolliency, etc. to the cosmetic as long as it satisfies the content of the slurry-like dispersion shown in the present invention for preparing the slurry-like dispersion, can be separately blended into the cosmetic as other optional components described later as a liquid oily component.
[0031] Component (C) of the present invention greatly affects the stability and feel of use of the cosmetic. When the ratio of silicone in component (C) is large, it is preferable in terms of compatibility with component (A), wettability to component (B), swelling property of component (D) described later, and compatibility with other components, but it is difficult to obtain an adhesion feeling. By reducing the ratio of silicone in component (C), an adhesion feeling can be obtained, but the above-mentioned compatibility, wettability, and swelling property decrease, and color unevenness is likely to occur. In addition, good dispersibility can be obtained by the production method of the present invention described later. When an adhesion feeling is desired, the ratio of non-silicone in component (C) is preferably 30% by mass or more, more preferably 50% by mass or more, even more preferably 80% by mass or more, and most preferably 100% by mass. The blending amount of silicone is preferably 15% by mass or less, more preferably 6% by mass or less, even more preferably 1% by mass or less, and most preferably not blended, and it is possible to achieve both an adhesion feeling and suppression of color unevenness.
[0032] [Optional Components] The slurry-like dispersion of the present invention may contain a film-forming agent, powder, ultraviolet scattering agent, ultraviolet absorber, oily agent that is not liquid, and component (D) described later. From the viewpoints of pigment dispersibility and suppression of the decrease in the concentration of component (A), Minute ( A) 、It is preferably composed of only component (B) and component (C).
[0033] [Method for producing a slurry-like dispersion] The method for producing the slurry-like dispersion of the present invention comprises a step (I) of mixing at least one selected from (A) trimethylsiloxysilicic acid and its derivatives, (B) a hydrophobized coloring pigment, and (C) an oily agent that is liquid at 25°C to prepare a slurry-like dispersion.
[0034] When preparing the slurry-like dispersion according to the present invention, there are no particular limitations on the method and apparatus, and it can be carried out by known methods. For example, any stirrer, grinder, mixer, disperser, etc., such as a Henschel mixer, ball mill, kneader, planetary mixer, ribbon blender, disperser mixer, homomixer, roll mill, etc., can be used. In particular, from the viewpoint of mixing efficiency, it is preferable to use a three-roll mill for mixing and stirring. The stirring and mixing temperature is not particularly limited, and 20°C to 105°C is preferable, and room temperature is particularly more preferable.
[0035] II. Cosmetics The cosmetics of the present invention contain 1 to 30% by mass of the above slurry-like dispersion in the cosmetics, more preferably 4 to 25% by mass, and even more preferably 10 to 25% by mass. The cosmetics may be water-in-oil type emulsified cosmetics or oil-in-water type emulsified cosmetics, but water-in-oil type emulsified cosmetics are preferable from the viewpoint of adhesion, and examples include milk-like, cream-like, stick-like, solid-like, etc. Specific cosmetics include makeup bases, concealers, liquid foundations, cream foundations, solid foundations, blushes, eyeshadows, mascaras, eyeliners, eyebrows, lipsticks, etc. made by blending the above cosmetic components, and sunscreen emulsions and sunscreen creams containing hydrophobized coloring pigments, etc. Among these, in particular, foundations, makeup bases, and sunscreens containing multiple types of coloring pigments for the purpose of applying to the skin are preferable.
[0036] [Component (D)] In the case of the cosmetic of the present invention, particularly in the case of an oil-in-water type emulsified cosmetic, it is preferable to blend the component (D) an organically modified clay mineral from the viewpoint of improving the pigment dispersion stability (suppressing color separation). The organically modified clay mineral can be used alone or in combination of two or more. The organically modified clay mineral is not particularly limited as long as it is used in ordinary cosmetics. For example, cationically modified clay minerals substituted with quaternary ammonium ions can be mentioned. Specifically, layered clay minerals such as bentonite, laponite, hectorite, montmorillonite, and magnesium aluminum silicate are treated with a quaternary ammonium salt type cationic surfactant so that the sodium ions between the layers of the layered clay mineral are replaced with quaternary ammonium ions, and cationically modified clay minerals can be used.
[0037] More specifically, dimethyldistearylammonium hectorite, dimethyldistearylammonium bentonite, benzyldimethylstearylammonium hectorite, etc. are preferable, and dimethyldistearylammonium hectorite is more preferable. Also, as commercially available products, Benton 38, Benton 38VCG, Benton 27 (manufactured by Elementis), etc. can be mentioned.
[0038] The content of the component (D) is preferably 1.5% by mass or less as the amount in the whole cosmetic. That is, the component (D) does not necessarily have to be blended within the range where the effects of the present invention are exhibited. However, when it is desired to have excellent adhesion to the skin and form a uniform thin film on the skin, 1.5% by mass or less (0 to 1.5% by mass) in the whole cosmetic is preferable, and 0.1 to 0.8% by mass is more preferable. From the viewpoint of suppressing the influence on the usability due to the component (D), 0.4% by mass or less is preferable. Even when the component (D) is not blended, good dispersibility can be obtained in the case of the slurry-like dispersion of the present invention. When blended in an amount exceeding 1.5% by mass, the film quality formed on the skin may become non-uniform, or the stability of the cosmetic over time in terms of quality may deteriorate.
[0039] Various optional components used in ordinary cosmetics can be blended in the cosmetic of the present invention.
[0040] As other optional components, for example, (1) an oil agent, (2) a compound having an alcoholic hydroxyl group, (3) a surfactant, (4) a powder, (5) a composition comprising a crosslinked organopolysiloxane and an oil agent that is liquid at room temperature, (6) a film-forming agent, (7) an antiperspirant, (8) an antibacterial agent, and (9) other additives may be included. These can be used alone or in appropriate combinations of two or more kinds.
[0041] (1) Oil-based component The oil-based component may be solid, semi-solid, or liquid. For example, natural animal and vegetable oils and fats and semi-synthetic oils, hydrocarbon oils, higher fatty acids, higher alcohols, esters, etc., silicone other than the above organosiloxane which is an essential component for the expression of the effects of the present invention, and fluorine-based oil agents can be used.
[0042] · Solid oil-based component In the present invention, when it is desired to solidify the cosmetic, it is preferable to blend wax, hydrocarbon, ester, higher alcohol, and higher fatty acid that are solid at 25°C. The oil-based component that is solid at 25°C preferably has a melting point of 40°C or higher, more preferably 60 to 110°C, and examples include wax, hydrocarbon, ester, higher alcohol, and higher fatty acid. There is no particular limitation as long as it is a raw material that can be usually blended in cosmetics. Specifically, vegetable waxes such as carnauba wax, candelilla wax, rice wax, and wood wax, animal waxes such as beeswax and whale wax, hydrocarbon waxes such as solid paraffin, polyethylene, ceresin, ozokerite, and microcrystalline wax, higher alcohols such as stearyl alcohol, behenyl alcohol, and cetyl alcohol, fatty acids such as stearic acid and behenic acid, and silicone waxes such as acrylic-silicone graft or block copolymer acrylic silicone resins (manufactured by Shin-Etsu Chemical Co., Ltd.: acrylic-silicone graft copolymer: KP-561P, 562P, etc.), or derivatives thereof can be mentioned, and it is preferable to be one or more selected from these.
[0043] · Natural animal and vegetable oils and fats and semi-synthetic oils Examples of natural animal and plant oils and semi-synthetic oils include squalane, squalene, avocado oil, linseed oil, almond oil, eno oil, olive oil, cocoa butter, kapok wax, kaya oil, carnauba wax, candelilla wax, refined candelilla wax, kounin oil, wheat germ oil, sesame oil, rice germ oil, rice bran oil, sugarcane wax, camellia oil, safflower oil, shea butter, sinagiri oil, cinnamon oil, jojoba wax, soybean oil, tea seed oil, camellia japonica oil, evening primrose oil, corn oil, rapeseed oil, Japan cedar oil, rice bran wax, germ oil, persic oil, palm oil, palm kernel oil, castor oil, sunflower oil, grape oil, bayberry wax, jojoba oil, macadamia nut oil, meadowfoam oil, cottonseed oil, cotton wax, candelilla wax, candelilla wax kernel oil, montan wax, coconut oil, peanut oil and other natural plant oils, as well as spermaceti wax, shellac wax, cod liver oil, beef tallow, beef foot tallow, beef bone fat, whale wax, turtle oil, lard, horse fat, beeswax, mink oil, mutton fat, lanolin, egg yolk oil and other natural animal oils (including those derived from insects), hydrogenated castor oil, methyl ester of castor oil fatty acid, hydrogenated palm oil, glyceride of fatty acid of triolein, hydrogenated beef tallow, hydrogenated oil, liquid lanolin, reduced lanolin, lanolin alcohol, hard lanolin, lanolin acetate, lanolin acetate alcohol, isopropyl lanolin fatty acid, polyoxyethylene lanolin alcohol ether, polyoxyethylene lanolin alcohol acetate, polyethylene glycol lanolin fatty acid, polyoxyethylene hydrogenated lanolin alcohol ether and other semi-synthetic oils.
[0044] In addition, among the ultraviolet absorbers described below, when they are liquid at 25°C, for example, ethylhexyl methoxycinnamate, octyl salicylate, octocrylene, etc. can be formulated into cosmetics as the above non-silicones.
[0045] (2) Compounds having an alcoholic hydroxyl group Examples of compounds having an alcoholic hydroxyl group include ethanol, isopropanol and other lower alcohols preferably having 2 to 5 carbon atoms, sugar alcohols such as sorbitol and maltose, and sterols such as cholesterol, sitosterol, phytosterol and lanosterol.
[0046] (3) Surfactant Surfactants include nonionic, anionic, cationic, and amphoteric surfactants, but are not particularly limited, and any surfactant can be used as long as it is used in ordinary cosmetics. Among these surfactants, partially crosslinked polyether-modified silicone, partially crosslinked polyglycerin-modified silicone, linear or branched polyoxyethylene-modified organopolysiloxane, linear or branched polyoxyethylene polyoxypropylene-modified organopolysiloxane, linear or branched polyoxyethylene-alkyl co-modified organopolysiloxane, linear or branched polyoxyethylene polyoxypropylene-alkyl co-modified organopolysiloxane, linear or branched polyglycerin-modified organopolysiloxane, and linear or branched polyglycerin-alkyl co-modified organopolysiloxane are preferred. In these surfactants, the content of the hydrophilic polyoxyethylene group, polyoxyethylene polyoxypropylene group, or polyglycerin residue preferably accounts for 10 to 70% by mass in the molecule. Further, when using partially crosslinked polyether-modified silicone or partially crosslinked polyglycerin-modified silicone, in a composition composed of the crosslinked organopolysiloxane and a liquid oil agent at room temperature, the crosslinked organopolysiloxane preferably swells containing the liquid oil agent of its own weight or more with respect to the liquid oil. As the liquid oil agent, liquid silicone, hydrocarbon oil, ester oil, natural animal and vegetable oil, semi-synthetic oil, etc. in the optional component oil agent, fluorine-based oil can be used. For example, 0.65 to 100 mm 2Low-viscosity silicone at 25°C, hydrocarbon oils such as liquid paraffin, squalane, isododecane, and isohexadecane, glyceride oils such as trioctanoin, ester oils such as isotridecyl isononanoate, N-acylglutamic acid ester, and lauroyl sarcosine ester, and natural animal and vegetable oils such as macadamia nut oil can be mentioned. Specific examples include those manufactured by Shin-Etsu Chemical Co., Ltd.: KSG-210, 240, 310, 320, 330, 340, 320Z, 350Z, 710, 810, 820, 830, 840, 820Z, 850Z, etc. Specific examples of surfactants that are not cross-linked organopolysiloxanes include those manufactured by Shin-Etsu Chemical Co., Ltd.: KF-6011, 6013, 6043, 6017, 6028, 6038, 6048, 6100, 6104, 6105, 6106, etc. In any case, the blending amount of the surfactant is preferably 0.1 to 20% by mass of the total cosmetics. If it is 0.1% by mass or more, the functions of dispersion and emulsification can be sufficiently achieved, and if it is 20% by mass or less, it is preferable because there is no risk that the cosmetics will have a sticky feeling when used. The HLB of the surfactant is not limited, but is preferably 2 to 14.5 for the purpose of maintaining the water resistance of the cosmetics.
[0047] (4) Powders As powders, in addition to the hydrophobically treated coloring pigments, inorganic powders, metal powders, organic powders, inorganic-organic composite powders, etc. can be mentioned. Specifically, it is as follows. However, the above component (B) is excluded.
[0048] · Inorganic powders Examples of the inorganic powder include fine particles composed of zirconium oxide, zinc oxide, cerium oxide, magnesium oxide, barium sulfate, calcium sulfate, magnesium sulfate, calcium carbonate, magnesium carbonate, talc, cleaved talc, mica, kaolin, sericite, muscovite, synthetic mica, phlogopite, red mica, biotite, lithium mica, silicic acid, silicon dioxide, fumed silica, hydrated silicon dioxide, aluminum silicate, magnesium silicate, aluminum magnesium silicate, calcium silicate, barium silicate, strontium silicate, metal tungstate, hydroxyapatite, vermiculite, hydrillaite, bentonite, montmorillonite, hectorite, zeolite, ceramics, dicalcium phosphate, alumina, aluminum hydroxide, boron nitride, boron boride, glass, etc. Examples of the inorganic colored pearl pigment include pearl pigments such as titanium oxide-coated mica, bismuth oxychloride, titanium oxide-coated bismuth oxychloride, titanium oxide-coated talc, fish scale foil, titanium oxide-coated colored mica, etc.
[0049] · Metal powder Examples of the metal powder include metal fine particles composed of, for example, aluminum, copper, stainless steel, silver, etc.
[0050] · Organic powder Examples of the organic powder include powders composed of silicone, polyamide, polyacrylic acid / acrylic acid ester, polyester, polyethylene, polypropylene, polystyrene, styrene / acrylic acid copolymer, divinylbenzene / styrene copolymer, polyurethane, vinyl resin, urea resin, melamine resin, benzoguanamine, polymethylbenzoguanamine, tetrafluoroethylene, polymethyl methacrylate (e.g., polymethyl acrylate, etc.), cellulose, silk, nylon, phenol resin, epoxy resin, polycarbonate, etc. In particular, examples of silicone include silicone resin particles (specific examples include KMP-590, 591, 592, etc. manufactured by Shin-Etsu Chemical Co., Ltd.) and silicone resin-coated silicone rubber powders (specific examples include KSP-100, 101, 102, 105, 300, 411, 441, etc. manufactured by Shin-Etsu Chemical Co., Ltd.). Also, metal soaps, etc. are included, and specific examples include powders composed of zinc stearate, aluminum stearate, calcium stearate, magnesium stearate, zinc myristate, magnesium myristate, zinc cetyl phosphate, calcium cetyl phosphate, sodium zinc cetyl phosphate, etc. Furthermore, organic dyes, etc. are included, and specific examples include tar dyes such as Red No. 3, Red No. 104, Red No. 106, Red No. 201, Red No. 202, Red No. 204, Red No. 205, Red No. 220, Red No. 226, Red No. 227, Red No. 228, Red No. 230, Red No. 401, Red No. 505, Yellow No. 4, Yellow No. 5, Yellow No. 202, Yellow No. 203, Yellow No. 204, Yellow No. 401, Blue No. 1, Blue No. 2, Blue No. 201, Blue No. 404, Green No. 3, Green No. 201, Green No. 204, Green No. 205, Orange No. 201, Orange No. 203, Orange No. 204, Orange No. 206, Orange No. 207, etc., and natural dyes such as carminic acid, laccaic acid, carthamin, brazilein, crocin, etc.
[0051] ·Inorganic-organic composite powder Examples of the inorganic-organic composite powder include composite powders in which the surface of the inorganic powder is coated with an organic powder by a publicly known and commonly used method.
[0052] In addition, as the powder described above, those with a treated particle surface can also be used. Further, the surface treatment agent preferably can impart hydrophobicity from the viewpoint of the water resistance of the cosmetic, and the treatment agent for imparting this hydrophobicity is not particularly limited, and examples thereof include silicone treatment agents, waxes, paraffins, organic fluorine compounds such as perfluoroalkyl and phosphates, surfactants, amino acids such as N-acylglutamic acid, and metal soaps such as aluminum stearate and magnesium myristate. More preferably, it is a silicone treatment agent, and examples thereof include caprylyl silane (manufactured by Shin-Etsu Chemical Co., Ltd.: AES-3083), or silanes or silylating agents such as trimethoxysilyl dimethicone, dimethyl silicone (manufactured by Shin-Etsu Chemical Co., Ltd.: KF-96A series), methyl hydrogen type polysiloxane (manufactured by Shin-Etsu Chemical Co., Ltd.: KF-99P, KF-9901, etc.), silicone branched type silicone treatment agents (manufactured by Shin-Etsu Chemical Co., Ltd.: KF-9908, KF-9909, etc.), acrylic silicone (manufactured by Shin-Etsu Chemical Co., Ltd.: KP-574, KP-541), and the like. Furthermore, the above surface hydrophobizing treatment agent may be used alone or in combination of two or more.
[0053] (5) Composition comprising a crosslinked organopolysiloxane and an oil agent that is liquid at room temperature In the composition comprising a crosslinked organopolysiloxane and an oil agent that is liquid at room temperature, the crosslinked organopolysiloxane preferably swells by containing the liquid oil agent having a weight equal to or more than its own weight with respect to the liquid oil. As the liquid silicone, hydrocarbon oil, ester oil, natural animal and vegetable oil, semi-synthetic oil, etc., fluorine-based oil in the optional component oil agent can be used. For example, 0.65 to 100 mm 2Low-viscosity silicone at / s(25°C), hydrocarbon oils such as liquid paraffin, squalane, isododecane, and isohexadecane, glyceride oils such as trioctanoin, ester oils such as isotridecyl isononanoate, N-acylglutamic acid ester, and lauroyl sarcosine ester, and natural animal and vegetable oils such as macadamia nut oil can be mentioned. The (5) component is a compound that does not have a polyether or polyglycerin structure in its molecular structure, different from the (3) component according to the present invention. Specific examples include those manufactured by Shin-Etsu Chemical Co., Ltd.: KSG series (trade name), particularly, KSG-15, 16, 016F, 19, 41, 42, 43, 44, 042Z, 045Z, etc.
[0054] (6) Film-forming agent The film-forming agent is mainly formulated for the purpose of further maintaining the effect persistence of the cosmetic. Although not particularly limited, it is preferably a silicone-based composition from the viewpoint of imparting water repellency. Specifically, trimethylsiloxysilicic acid, acrylic-silicone film-forming agent, silicone-modified norbornene, silicone-modified pullulan, etc. can be used. The said film-forming agent may be dissolved in a liquid oil agent at room temperature in advance and then formulated into the cosmetic. As the said liquid oil agent, liquid silicone, hydrocarbon, ester, natural animal and vegetable oil, semi-synthetic oil, fluorine-based oil, etc. in the oil agent of optional components can be used. For example, 0.65~100mm 2 Low-viscosity silicone at / s(25°C), hydrocarbon oils such as liquid paraffin, squalane, isododecane, and isohexadecane, glyceride oils such as trioctanoin, ester oils such as isotridecyl isononanoate, N-acylglutamic acid ester, and lauroyl sarcosine ester, and natural animal and vegetable oils such as macadamia nut oil can be mentioned. Further, specific examples thereof include KF-7312J, which is a silicone-dissolved product of trimethylsiloxysilicic acid, KP-545 and KP-549, which are silicone-dissolved products of acrylic-silicone film-forming agents, NBN-30-ID, which is an isododecane-dissolved product of silicone-modified norbornene, TSPL-30-ID, which is an isododecane-dissolved product of silicone-modified pullulan, and TSPL-30-D5, which is a silicone-dissolved product, all manufactured by Shin-Etsu Chemical Co., Ltd.
[0055] (7) Antiperspirant When the cosmetic according to the present invention is a deodorant agent, an antiperspirant can be optionally blended. The antiperspirant is not particularly limited as long as it is a component that suppresses the generation of sweat by astringing the skin, and general-purpose components can be widely used. For example, chlorhydroxyaluminum, aluminum chloride, allantoin chlorhydroxyaluminum, allantoin aluminum salt, tannic acid, potassium aluminum sulfate, zinc oxide, zinc paraphenolsulfonate, burnt alum, tetrachloro(Al / zirconium) hydrate, trichlorohexaglycine(Al / zirconium), etc. can be mentioned. In particular, as a component that exhibits a high effect, preferably, it is an antiperspirant active ingredient selected from the group consisting of aluminum halides, hydroxyaluminum halides, and complexes or mixtures thereof with zirconyl oxyhalide and zirconyl hydroxyhalide. These antiperspirants can be dissolved in water and blended, or the powder can be directly blended into the formulation and used. Commercially available products can also be used as the antiperspirant. The commercially available products used may be in the form of a mixed raw material with other components. The content of the antiperspirant is not particularly limited and can be appropriately changed according to the blending amounts of other components. For the purpose of obtaining a deodorant agent with excellent antiperspirant effect and for the purpose of obtaining a deodorant agent with reduced irritation to the skin, its content is preferably in the range of 0.001 to 30% by mass, more preferably in the range of 0.01 to 20% by mass, based on the total amount of the deodorant agent.
[0056] (8) Antibacterial agent As long as the antibacterial agent can obtain an anti-odor effect by suppressing the growth of the resident bacteria on the skin that produce the causative substances of body odor, there is no particular limitation. For example, antibacterial agents such as triclosan, benzalkonium chloride, benzethonium chloride, chlorhexidine hydrochloride, chlorhexidine gluconate, halocarban, and isomethylphenol are generally used. Also, it may be blended with essential oils or extracts derived from Chinese herbal medicines such as green tea dry distillation extract, which have antibacterial properties. Examples of antibacterial agents with anti-odor effects derived from Chinese herbal medicines include green tea extract, lavender extract, safflower extract, turmeric extract, large-leaf magnolia bark extract, sea wormwood extract, aloe vera extract, clara root extract, sasakusa leaf extract, garlic extract, witch hazel extract, black tea extract, sage leaf extract, sansho extract, ginger root extract, zephyr lily root extract, ivy extract, houttuynia cordata extract, peach fruit extract, peach leaf extract, peppermint leaf extract, cnidium officinale extract, eucalyptus leaf extract, castor bean seed coat extract, jujube extract, polygala tenuifolia extract, etc. The plant extracts may be used alone or in combination of two or more.
[0057] (9) Other additives Examples of other additives include oil-soluble gelling agents, ultraviolet absorption and scattering agents, moisturizers, preservatives, fragrances, salts, antioxidants, pH adjusters, chelating agents, cooling agents, anti-inflammatory agents, skin beautifying ingredients (whitening agents, cell activators, roughness improvers, blood circulation promoters, skin astringents, anti-seborrheic agents, etc.), vitamins, amino acids, nucleic acids, hormones, inclusion compounds, etc.
[0058] · Oil-soluble gelling agent Examples of the oil-soluble gelling agent include metal soaps such as aluminum stearate, magnesium stearate, and zinc myristate; amino acid derivatives such as N-lauroyl-L-glutamic acid and α,γ-di-n-butylamine; dextrin fatty acid esters such as dextrin palmitate, dextrin stearate, and dextrin palmitate 2-ethylhexanoate; sucrose fatty acid esters such as sucrose palmitate and sucrose stearate; fructooligosaccharide fatty acid esters such as fructooligosaccharide stearate and fructooligosaccharide 2-ethylhexanoate; and benzylidene derivatives of sorbitol such as monobenzylidene sorbitol and dibenzylidene sorbitol.
[0059] · Ultraviolet absorption and scattering agent In the present invention, when a cosmetic is desired to have an ultraviolet shielding effect, it is preferable to incorporate an ultraviolet absorber.
[0060] The ultraviolet absorber is not particularly limited as long as it is a raw material that can be usually formulated in cosmetics. Specifically, homomethyl salicylate, octocrylene, t-butyl methoxydibenzoylmethane, 4-(2-β-glucopyranosyloxy)propoxy-2-hydroxybenzophenone, octyl salicylate, diethylamino hydroxybenzoyl hexyl benzoate, oxybenzone-6, oxybenzone-9, oxybenzone-1, polysilicone-15, 1-(3,4-dimethoxyphenyl)-4,4-dimethyl-1,3-pentanedione, octyl dimethoxybenzylidene dioxoimidazolidine propionate, oxybenzone-2, terephthalylidene dicamphor sulfonic acid, 2,4,6-tris[4-(2-ethylhexyloxycarbonyl)anilino]-1,3,5-triazine, methyl trimethoxycinnamate bis(trimethylsiloxy)silyl isopentyl, droxmetrizole trisiloxane, 2-ethylhexyl p-dimethylaminobenzoate, isopropyl p-methoxycinnamate, ethylhexyl methoxycinnamate, bis-ethylhexyloxyphenol methoxyphenyl triazine, oxybenzone-3, oxybenzone-4, oxybenzone-5, phenylbenzimidazole sulfonic acid, methylene bisbenzotriazolyl tetramethylbutylphenol, etc. can be mentioned. Further, it is possible to use a UVA absorber (for example, diethylamino hydroxybenzoyl hexyl benzoate, etc.) and a UVB absorber (for example, ethylhexyl methoxycinnamate, etc.) in combination, and it is also possible to arbitrarily combine them.
[0061] Among these, if it is one or more organic ultraviolet absorbers selected from ethylhexyl methoxycinnamate, diethylamino hydroxybenzoyl hexyl benzoate, octyl salicylate, polysilicone-15, t-butyl methoxydibenzoylmethane, oxybenzone, methylene bisbenzotriazolyl tetramethylbutylphenol, bis-ethylhexyloxyphenol methoxyphenyl triazine and octocrylene, it is particularly preferable from the viewpoint of compatibility with oil agents.
[0062] Examples of the ultraviolet light scattering agent include particles that absorb and scatter ultraviolet light, such as fine particle titanium oxide, fine particle iron-containing titanium oxide, fine particle zinc oxide, fine particle cerium oxide, and their composites. It is also possible to use a dispersion in which these particles that absorb and scatter ultraviolet light are dispersed in an oil agent in advance. As the oil agent, a fluorine-based oil can be used, such as liquid silicone, hydrocarbon oil, ester oil, natural animal and vegetable oil, semi-synthetic oil, etc. in an oil agent of optional components. For example, 0.65~100mm 2 / s (25 °C) low-viscosity silicone, hydrocarbon oils such as liquid paraffin, squalane, isododecane, isohexadecane, glyceride oils such as trioctanoin, ester oils such as isotridecyl isononanoate, N-acylglutamic acid ester, lauroyl sarcosine ester, and natural animal and vegetable oils such as macadamia nut oil can be mentioned. Specific examples of the dispersion in which particles that absorb and scatter ultraviolet light are dispersed in an oil agent in advance include: SPD series (trade name) manufactured by Shin-Etsu Chemical Co., Ltd., particularly SPD-T5, Z5, T6, Z6, T7, etc.
[0063] · Humectant Examples of the humectant include glycerin, sorbitol, propylene glycol, dipropylene glycol, 1,3-butylene glycol, pentylene glycol, glucose, xylitol, maltitol, polyethylene glycol, hyaluronic acid, chondroitin sulfate, pyrrolidone carboxylate, polyoxyethylene methyl glucoside, polyoxypropylene methyl glucoside, egg yolk lecithin, soybean lecithin, phosphatidylcholine, phosphatidylethanolamine, phosphatidylserine, phosphatidylglycerol, phosphatidylinositol, sphingomyelin lipid, etc.
[0064] · Preservative Examples of preservatives include alkyl para - hydroxybenzoates, benzoic acid, sodium benzoate, sorbic acid, potassium sorbate, phenoxyethanol, etc. Examples of antibacterial agents include benzoic acid, salicylic acid, phenol, sorbic acid, alkyl para - hydroxybenzoates, parachlorometacresol, hexachlorophene, trichlorocarbanilide, photosensitizers, phenoxyethanol, etc.
[0065] · Fragrance Fragrances include natural fragrances and synthetic fragrances. Natural fragrances include plant - based fragrances separated from flowers, leaves, woods, fruit peels, etc.; animal - based fragrances such as musk and civet. Synthetic fragrances include hydrocarbons such as monoterpenes, alcohols such as aliphatic alcohols and aromatic alcohols, aldehydes such as terpene aldehydes and aromatic aldehydes, ketones such as alicyclic ketones, esters such as terpene - based esters, lactones, phenols, oxides, nitrogen - containing compounds, acetals, etc.
[0066] · Salts Salts include inorganic salts, organic acid salts, amine salts, and amino acid salts. Examples of inorganic salts include sodium salts, potassium salts, magnesium salts, calcium salts, aluminum salts, zirconium salts, zinc salts, etc. of inorganic acids such as hydrochloric acid, sulfuric acid, carbonic acid, nitric acid, etc.; examples of organic acid salts include salts of organic acids such as acetic acid, dehydroacetic acid, citric acid, malic acid, succinic acid, ascorbic acid, stearic acid, etc.; examples of amine salts and amino acid salts include salts of amines such as triethanolamine and salts of amino acids such as glutamic acid. In addition, other salts such as hyaluronic acid, chondroitin sulfate, aluminum zirconium glycine complex, and further, acid - alkali neutralization salts used in cosmetic formulations can also be used.
[0067] · Antioxidants The antioxidant is not particularly limited, and examples thereof include carotenoids, ascorbic acid and its salts, ascorbyl stearate, tocopheryl acetate, tocopherol, p-t-butylphenol, butylhydroxyanisole, dibutylhydroxytoluene, phytic acid, ferulic acid, thiotaurine, hypotaurine, sulfite, erythorbic acid and its salts, chlorogenic acid, epicatechin, epigallocatechin, epigallocatechin gallate, apigenin, kaempferol, myricetin, quercetin, etc. The antioxidant may be used alone or in combination of two or more kinds.
[0068] ·pH adjuster Examples of the pH adjuster include lactic acid, citric acid, glycolic acid, succinic acid, tartaric acid, dl-malic acid, potassium carbonate, sodium hydrogen carbonate, ammonium hydrogen carbonate, etc.
[0069] ·Chelating agent Examples of the chelating agent include alanine, sodium edetate, sodium polyphosphate, sodium metaphosphate, phosphoric acid, etc.
[0070] ·Cooling agent Examples of the cooling agent include L-menthol, camphor, etc.
[0071] ·Anti-inflammatory agent Examples of the anti-inflammatory agent include allantoin, glycyrrhizic acid and its salts, glycyrrhetinic acid and stearyl glycyrrhetinate, tranexamic acid, azulene, etc.
[0072] ·Ingredient for beautifying skin As beauty ingredients, there are whitening agents such as placenta extract, arbutin, glutathione, and extract of Saxifraga stolonifera, cell activators such as royal jelly, photosensitizer, cholesterol derivatives, and extract of calf blood; skin roughness improvers, wareninyl nonanoate, benzyl nicotinate, β-butoxyethyl nicotinate, capsaicin, gingerol, cantharidin, ichthyol, caffeine, tannic acid, α-borneol, tocopherol nicotinate, inositol hexanicotinate, cyclandelate, cinnarizine, tolazoline, acetylcholine, verapamil, cephalanthin, γ-oryzanol, etc. as blood circulation accelerators, zinc oxide, tannic acid, etc. as skin astringents, sulfur, tiopronin, etc. as anti-seborrheic agents, etc.
[0073] · Vitamins Vitamins include vitamin A oils, retinol, retinol acetate, retinol palmitate, etc. as vitamin A group, riboflavin, riboflavin butyrate, flavin adenine nucleotide, etc. as vitamin B2 group, pyridoxine hydrochloride, pyridoxine dioctanoate, pyridoxine tripalmitate, etc. as vitamin B6 group, vitamin B12 and its derivatives, vitamin B15 and its derivatives, etc. as vitamin B group, L-ascorbic acid, L-ascorbic acid dipalmitate, L-ascorbic acid-2-sodium sulfate, L-ascorbic acid phosphate diester dipotassium, etc. as vitamin C group, ergocalciferol, cholecalciferol, etc. as vitamin D group, α-tocopherol, β-tocopherol, γ-tocopherol, dl-α-tocopherol acetate, dl-α-tocopherol nicotinate, dl-α-tocopherol succinate, etc. as vitamin E group; nicotinic acid, benzyl nicotinate, nicotinamide, etc. as nicotinic acid group, vitamin H, vitamin P, calcium pantothenate, D-pantothenyl alcohol, pantothenyl ethyl ether, acetyl pantothenyl ethyl ether, etc. as pantothenic acid group, biotin, etc.
[0074] · Amino acids Examples of amino acids include glycine, valine, leucine, isoleucine, serine, threonine, phenylalanine, arginine, lysine, aspartic acid, glutamic acid, cystine, cysteine, methionine, tryptophan and the like.
[0075] · Nucleic acid Examples of nucleic acids include deoxyribonucleic acid and the like.
[0076] · Hormone Examples of hormones include estradiol, ethenyl estradiol and the like.
[0077] · Inclusion compound Examples of inclusion compounds include cyclodextrin and the like.
[0078] [Method for producing cosmetics] Examples of the method for producing the cosmetics of the present invention include those having the following steps. (A) Step (I) of preparing a slurry-like dispersion by mixing one or more selected from trimethylsiloxysilicic acid and its derivatives, (B) a hydrophobized coloring pigment, and (C) an oily agent that is liquid at 25°C. Step (II-1) of mixing the obtained slurry-like dispersion with an oil phase component and then mixing an aqueous phase component with the obtained mixture II-1, or Step (II-2) of mixing an oil phase component and an aqueous phase component and then mixing the slurry-like dispersion with the obtained mixture II-2 A method for producing an oil-in-water type emulsified cosmetic having these steps.
[0079] As described above, by having step (I) of preparing a slurry-like dispersion in advance, the dispersibility of component (B) can be improved, and color separation after step II-1 or II-2 can be more suppressed.
[0080] In addition, the oil-phase component in the present invention refers to a component that constitutes a continuous phase, which is a medium (outer phase) in which emulsion particles are dispersed in the resulting water-in-oil type emulsified cosmetic, and excludes components in the form of a slurry-like dispersion. Further, an emulsifier that is blended for the purpose of emulsification and is dissolved or dispersed in an oily component is also regarded as an oil-phase component. On the other hand, the water-phase component refers to a component that constitutes a dispersed phase serving as emulsion particles (inner phase).
[0081] In the steps (II-1) and (II-2) above, in addition to the step (I) of preparing the slurry-like dispersion, the mixing device and the like include stirrers such as paddles, propellers, and mixers. The mixing temperature is not particularly limited, and 20 to 105°C is preferable, and room temperature is more preferable. As the steps (II-1) and (II-2), when the oil-phase component is 5 to 50% by mass, (II-1) is preferable from the viewpoint of the ease of transferring the water phase, and when the oil-phase component is 10 to 80% by mass, (II-2) is preferable from the viewpoint of the viscosity during emulsification. When it is desired to reduce the influence of the components of the cosmetic on the slurry-like dispersion, (II-2) is preferable.
Examples
[0082] Hereinafter, production examples, examples, and comparative examples will be shown to specifically illustrate the present invention, but the present invention is not limited to the following examples. In the following examples, unless otherwise specified, “%” of the composition indicates mass %, the ratio indicates mass ratio, the content is the blending amount of the described blended product, the ratio of the non-silicone that is liquid at 25°C in the component (C), the content of the components (A) to (C) in the slurry-like dispersion, and (A) / (B) is the ratio of pure components.
[0083] · Production Example of Trimethylsiloxysilicic Acid Derivative of Component (A) The trimethylsiloxysilicic acid derivatives (Production Examples 1 and 2) used in the cosmetic of the present invention were produced as follows.
[0084] [Production Example 1] Production Method of Glycerin-Modified Trimethylsiloxysilicic Acid / Isododecane: 60% Solids Solution 1,300 g of a 50% isododecane solution of a powdery hydrosilyl group-containing organosilicon resin represented by the average compositional formula (A1) (weight average molecular weight 4,480, hydrogen gas generation amount: 8.0 mL / g), 30.7 g of glycerin monoallyl ether represented by the formula (A2), 1,300 g of 2-propanol, and 0.7 g of a 0.5% solution of chloroplatinic acid in 2-propanol were charged into a reactor and reacted by heating at 100 °C for 6 hours. Thereafter, the solvent was distilled off by heating under reduced pressure. Further, after adding 325 g of ethanol, 6.5 g of a 5% aqueous sodium hydroxide solution was added to hydrolyze unreacted hydrosilyl groups, and then 0.8 g of concentrated hydrochloric acid was added for neutralization. After neutralization, 195 g of a 0.01 N hydrochloric acid aqueous solution was added to hydrolyze the allyl ether groups of unreacted polyoxyalkylene, and it was neutralized with 3.3 g of 5% aqueous sodium bicarbonate solution. The reaction product was heated under reduced pressure to distill off the solvent, and filtration was performed to obtain an isododecane solution of an organic group-modified organosilicon resin represented by the average compositional formula (A3). Average compositional formula (A1): (Me 3 SiO 1 / 2 ) 27.8 (HMe 2 SiO 1 / 2 ) 1.6 (SiO 2 ) 35.3 Formula (A2): CH 2 =CH-CH 2 -O-(CH 2 CH(OH)CH 2 O)-H Average compositional formula (A3): (Me 3 SiO 1 / 2 ) 27.8 (R 2 Me 2 SiO 1 / 2 ) 1.6 (SiO 4 / 2 ) 35.3 R 2 =-CH 2 -CH 2 -CH 2 -O-(CH 2 CH(OH)CH 2 O)-H
[0085] [Production Example 2] Method for producing polyether-modified trimethylsiloxysilicic acid / isododecane: 60% solids solution 1,000 g of a 50% isododecane solution of a powdery hydrogen silyl group-containing organosilicon resin (weight average molecular weight 4,210, hydrogen gas generation amount: 6.9 mL / g) represented by the average composition formula (A4), 69.1 g of polyoxyalkylene represented by the formula (A5), 1,000 g of 2-propanol, and 0.5 g of a 0.5% 2-propanol solution of chloroplatinic acid were charged into a reactor and reacted by heating at 80°C for 6 hours. Then, the solvent was distilled off by heating under reduced pressure. Further, after adding 250 g of ethanol, 5.0 g of a 5% aqueous sodium hydroxide solution was added to hydrolyze the unreacted hydrogen silyl groups, and then 0.6 g of concentrated hydrochloric acid was added for neutralization. After neutralization, 150 g of a 0.01N hydrochloric acid aqueous solution was added to hydrolyze the allyl ether groups of the unreacted polyoxyalkylene, and it was neutralized with 2.6 g of 5% aqueous sodium bicarbonate solution. The reaction product was heated under reduced pressure to distill off the solvent, and filtration was performed to obtain a 60% isododecane solution of an organic group-modified organosilicon resin represented by the average composition formula (A6). The isododecane solution of the obtained organic group-modified organosilicon resin was heated to 120 - 130°C under reduced pressure to remove isododecane, and the resulting product was a solid powder. Also, the HLB value of the product was 1.1. Average composition formula (A4): (Me 3 SiO 1 / 2 ) 25.4 (HMe 2 SiO 1 / 2 ) 1.3 (SiO 2 ) 34.3 Formula (A5): CH 2 =CH-CH 2 -O-(C 2 H 4 O) 3 -CH 3 Average composition formula (A6): (Me 3 SiO 1 / 2 ) 25.4 (R 2 Me 2 SiO 1 / 2 ) 1.3 (SiO 2) 34.3 R 2 =-CH 2 -CH 2 -CH 2 -O-(C 2 H 4 O) 3 -CH 3
[0086] The present invention will be specifically described below by giving formulation examples of Examples and Comparative Examples related to cosmetics, but the present invention is not limited to these Examples.
[0087] [Examples 1 to 9, Comparative Examples 1 to 10] Water-in-oil (W / O) foundation Regarding Examples 5 to 9, a water-in-oil (W / O) foundation was prepared according to the following production method using the trimethylsiloxysilicate derivatives obtained in Production Examples 1 and 2. The compositions of Examples 1 to 9 and Comparative Examples 1 to 10 are shown in Tables 1 to 4.
[0088] [Table 1] (Note 1) Manufactured by Shin-Etsu Chemical Co., Ltd.: KSG-210 (Mixture of 70 - 80% dimethylpolysiloxane + 20 - 30% crosslinked polyether-modified silicone) (Note 2) Manufactured by Shin-Etsu Chemical Co., Ltd.: KSG-15 (Mixture of 90 - 96% decamethylcyclopentasiloxane + 4 - 10% crosslinked dimethylpolysiloxane) (Note 3) Manufactured by Shin-Etsu Chemical Co., Ltd.: KF-6048 (Note 4) Manufactured by Shin-Etsu Chemical Co., Ltd.: KSP-101 (Note 5) Manufactured by Shin-Etsu Chemical Co., Ltd.: KF-7312K (Mixture of 40% dimethylpolysiloxane (6cs) + 60% trimethylsiloxysilicate) (Note 6) Manufactured by Shin-Etsu Chemical Co., Ltd.: KP-578 (Note 7) Manufactured by Shin-Etsu Chemical Co., Ltd.: KTP-09W, R, Y, B (KF-9909-treated colored inorganic pigments, W: white, R: red, Y: yellow, B: black)
[0089] (Manufacturing method) Components 1 to 7 were mixed uniformly (preparation of the oil phase component). To this, components 15 to 18 were gently added after being uniformly mixed (preparation of the aqueous phase component), and stirred to form an emulsion. Separately, components 8 to 14 were subjected to roller treatment (preparation of the slurry-like dispersion), and added to and mixed with the aforementioned emulsion. This was filled into a predetermined container to obtain a foundation.
[0090]
Table 2
[0091]
Table 3
[0092] The notes for Tables 2 and 3 are as follows. (Note 1) Manufactured by Shin-Etsu Chemical Co., Ltd.: KSG-310 (Mixture of 65 - 75% mineral oil + 25 - 35% crosslinked alkyl polyether-modified silicone) (Note 2) Manufactured by Shin-Etsu Chemical Co., Ltd.: KSG-41A (Mixture of 70 - 80% mineral oil + 20 - 30% crosslinked alkyl-modified silicone) (Note 3) Manufactured by Shin-Etsu Chemical Co., Ltd.: KF-6048 (Note 4) Manufactured by Shin-Etsu Chemical Co., Ltd.: KSP-101 (Note 5) Manufactured by Shin-Etsu Chemical Co., Ltd.: X-21-5595 (Mixture of 40% isododecane + 60% trimethylsiloxysilicic acid) (Note 6) Manufactured by Shin-Etsu Chemical Co., Ltd.: X-21-5616 (Mixture of 40% isododecane + 60% trimethylsiloxysilicic acid) (Note 7) Manufactured by Shin-Etsu Chemical Co., Ltd.: KP-578 (Note 8) Manufactured by Shin-Etsu Chemical Co., Ltd.: KF-6038 (Note 9) Manufactured by Shin-Etsu Chemical Co., Ltd.: KF-6105 (Note 10) Manufactured by Shin-Etsu Chemical Co., Ltd.: KF-6106 (Note 11) Manufactured by Shin-Etsu Chemical Co., Ltd.: KTP-09W, R, Y, B (KF-9909 treated colored inorganic pigment, W: white, R: red, Y: yellow, B: black)
[0093] (Manufacturing method) Components 1 to 8 were mixed uniformly (preparation of the oil phase component). To this, components 23 to 26 were uniformly mixed and then gently added (preparation of the aqueous phase component), and stirred to form an emulsion. Separately, components 9 to 22 were roller-treated (preparation of the slurry-like dispersion) and added to and mixed with the aforementioned emulsion. This was filled into a predetermined container to obtain a foundation.
[0094]
Table 4
[0095] (Manufacturing method) Components 1 to 6 were mixed uniformly (preparation of the oil phase component). Separately, components 7 to 13 were roller-treated (preparation of the slurry-like dispersion). This slurry-like dispersion was added to the previous oil phase component and uniformly mixed. Further, components 14 to 17 prepared separately (preparation of the aqueous phase component) were gently added thereto and stirred to form an emulsion. It was added to and mixed with the aforementioned emulsion. This was filled into a predetermined container to obtain a foundation.
[0096] Regarding the obtained water-in-oil (W / O) type foundation, a usage test was conducted by 10 female professional panelists on (1) usability (good feel; light feel), (2) spreadability (good elongation), (3) adhesion, and (4) pigment dispersibility, and evaluated according to the following evaluation criteria. The evaluation results of Examples 1 to 9 and Comparative Examples 1 to 10 are also shown in the table.
[0097] (Evaluation Criteria) 5 points: Very good (1), (2), (3), no color separation (4) 4 points: Good (1), (2), (3), almost no color separation (4) 3 points: Ordinary (1), (2), (3), slightly color separation (4) 2 points: Slightly poor (1), (2), (3), color separation (4) 1 point: Poor (1), (2), (3), very color separation (4) And for the obtained average score, it was judged with ○× according to the following criteria. (Judgment of Average Score) The obtained average score is 4.5 points or more ◎ The obtained average score is 3.5 points or more and less than 4.5 points ○ The obtained average score is 2.5 points or more and less than 3.5 points △ The obtained average score is 1.5 points or more and less than 2.5 points × The obtained average score is less than 1.5 points ×× ◎, ○, △ or above are considered qualified.
[0098] As is clear from the above results, the foundations of Examples 1 to 9 were demonstrated to suppress color separation while maintaining good usability and spreadability compared to Comparative Examples 1 to 10. When trying to obtain adhesion, color separation is likely to occur due to polar oil, but it was confirmed that the present invention suppresses the occurrence of color separation. Furthermore, it was effective when component (B) was a dispersion in which components (A) and (C) were dispersed in advance. In addition, although the blending of component (D) is effective in suppressing the occurrence of color separation, it was found that the blending amount of component (D) can be reduced by the present invention to improve the usability.
[0099] [Example 10] Foundation (water-in-oil emulsion cosmetic) A foundation was prepared according to the formulation shown in Table 5.
[0100] [Table 5] (Note 1) Manufactured by Shin-Etsu Chemical Co., Ltd.: KSG-320 (Mixture of 70 - 80% isododecane + 20 - 30% crosslinked alkyl polyether-modified silicone) (Note 2) Manufactured by Shin-Etsu Chemical Co., Ltd.: KSG-42A (Mixture of 75 - 85% isododecane + 15 - 25% crosslinked alkyl-modified silicone) (Note 3) Manufactured by Shin-Etsu Chemical Co., Ltd.: KF-6048 (Note 4) Manufactured by Shin-Etsu Chemical Co., Ltd.: KF-56A (Note 5) Manufactured by Shin-Etsu Chemical Co., Ltd.: X-21-5595 (Mixture of 40% isododecane + 60% trimethylsiloxysilicic acid) (Note 6) Manufactured by Shin-Etsu Chemical Co., Ltd.: TMF-1.5 (Note 7) Manufactured by Shin-Etsu Chemical Co., Ltd.: X-21-5616 (Mixture of 40% isododecane + 60% trimethylsiloxysilicic acid) (Note 8) Manufactured by Shin-Etsu Chemical Co., Ltd.: KTP-09W, R, Y, B (KF-9909-treated colored inorganic pigment, W: white, R: red, Y: yellow, B: black) (Manufacturing method) A: Components 1 - 9 were uniformly mixed (preparation of oil phase components). B: Components 16 - 21 were uniformly mixed (preparation of aqueous phase components). C: Components 10 - 15 were uniformly mixed and roll-treated (preparation of slurry-like dispersion). D: B was gradually added to A and emulsified, and then C was added to obtain a foundation. The foundation obtained as described above was found to have light spreadability, a smooth texture without stickiness, and excellent pigment dispersibility.
[0101] [Example 11] Makeup base (water-in-oil emulsion cosmetic) Using the formulation shown in Table 6, a makeup base was prepared.
[0102] [Table 6] (Note 1) Manufactured by Shin-Etsu Chemical Co., Ltd.: KSG-830 (Mixture of 75 - 85% isododecane + 15 - 25% crosslinked alkyl polyglycerin-modified silicone) (Note 2) Manufactured by Shin-Etsu Chemical Co., Ltd.: KSG-42A (Mixture of 75 - 85% isododecane + 15 - 25% crosslinked alkyl-modified silicone) (Note 3) Manufactured by Shin-Etsu Chemical Co., Ltd.: KF-6105 (Note 4) Manufactured by Shin-Etsu Chemical Co., Ltd.: SPD-T7 (Note 5) Manufactured by Shin-Etsu Chemical Co., Ltd.: SPD-Z5 (Note 6) Manufactured by Shin-Etsu Chemical Co., Ltd.: X-21-5595 (Mixture of 40% isododecane + 60% trimethylsiloxysilicic acid) (Note 7) Manufactured by Shin-Etsu Chemical Co., Ltd.: AES-3083 treatment (Manufacturing method) A: Components 1 - 8 were uniformly mixed (preparation of the oil phase component). B: Components 15 - 20 were uniformly mixed (preparation of the aqueous phase component). C: Components 9 - 14 were uniformly mixed and roll-treated (preparation of the slurry-like dispersion). D: B was gradually added to A and emulsified, and then C was added to obtain the makeup base. It was found that the makeup base obtained as described above had slight spreading and elongation, was smooth and non-greasy, and had excellent pigment dispersibility.
[0103] [Example 12] Foundation (water-in-oil emulsion cosmetic) Using the formulation shown in Table 7, a foundation was prepared.
[0104] [Table 7] (Note 1) Manufactured by Shin-Etsu Chemical Co., Ltd.: KSG-18A (Mixture of 80 - 90% diphenylsiloxyphenyltrimethicone + 10 - 20% crosslinked phenyl-modified silicone) (Note 2) Manufactured by Shin-Etsu Chemical Co., Ltd.: KF-6038 (Note 3) Manufactured by Shin-Etsu Chemical Co., Ltd.: KSP-300 (Note 4) Manufactured by Shin-Etsu Chemical Co., Ltd.: KP-561P (Note 5) Manufactured by Shin-Etsu Chemical Co., Ltd.: KP-550 (Solution of 60% isododecane + 40% acrylic silicone-based graft copolymer) (Note 6) Manufactured by Shin-Etsu Chemical Co., Ltd.: X-21-5595 (Mixture of 40% isododecane + 60% trimethylsiloxysilicic acid) (Note 7) Manufactured by Shin-Etsu Chemical Co., Ltd.: AES-3083 treatment (Manufacturing method) A: Components 1 - 8 were uniformly mixed at 90°C (preparation of oil phase components). B: Components 18 - 23 were uniformly mixed at 85°C (preparation of aqueous phase components). C: Components 9 - 17 were uniformly mixed and treated with a homomixer (preparation of slurry-like dispersion). D: At 85°C, B was slowly added to A and emulsified, and then C was added to obtain a solid foundation.
[0105] The solid foundation obtained as described above was found to have a light spread, be smooth and non-sticky, and have excellent pigment dispersibility.
[0106] [Example 13] Water-in-oil type mascara A water-in-oil type mascara was prepared with the formulation shown in Table 8.
[0107]
Table 8
[0108] The water-in-oil type mascara obtained as described above was found to have low spreadability, be smooth and non-sticky, and have excellent pigment dispersibility.
[0109] [Example 14] Water-in-oil type foundation A water-in-oil type foundation was prepared according to the formulation shown in Table 9.
[0110] [Table 9] (Note 1) Manufactured by Shin-Etsu Chemical Co., Ltd.: KSG-320Z (Mixture of 70 - 80% isododecane + 20 - 30% crosslinked alkyl polyether-modified silicone) (Note 2) Manufactured by Shin-Etsu Chemical Co., Ltd.: KSG-042Z (Mixture of 75 - 85% isododecane + 15 - 25% crosslinked alkyl-modified silicone) (Note 3) Manufactured by Shin-Etsu Chemical Co., Ltd.: KF-6048 (Note 4) Manufactured by Shin-Etsu Chemical Co., Ltd.: KF-6038 (Note 5) Manufactured by Shin-Etsu Chemical Co., Ltd.: KF-7312K (Mixture of 40% dimethylpolysiloxane (6 cs) + 60% trimethylsiloxysilicic acid) (Note 6) Manufactured by Shin-Etsu Chemical Co., Ltd.: KTP-09W, R, Y, B (KF-9909 treated colored inorganic pigments, W: white, R: red, Y: yellow, B: black) (Manufacturing method) A: Components 1 to 10 were uniformly mixed (preparation of oil phase component). B: Components 17 to 22 were uniformly mixed (preparation of aqueous phase component). C: Components 11 to 16 were uniformly mixed and roll-treated (preparation of slurry-like dispersion). D: C was added to A and uniformly mixed, then B was gradually added and emulsified to obtain a foundation.
[0111] It was found that the foundation obtained as described above has a light spreading property, is smooth and non-greasy, and also has excellent pigment dispersibility.
[0112] Note that the present invention is not limited to the above embodiments. The above embodiments are examples, and any configuration that has a substantially identical structure to the technical idea described in the claims of the present invention and exhibits the same operational effects is included in the technical scope of the present invention.
Claims
1. One or more selected from (A) trimethylsiloxysilicic acid and its derivatives, (B) a hydrophobized colored pigment, and (C) an oil agent that is liquid at 25°C A slurry-like dispersion containing the above components, wherein the content of component (A) is 0.1 to 10% by mass, the content of component (B) is 20 to 89.9% by mass, and the content of component (C) is 10 to 35% by mass.
2. The slurry-like dispersion according to Claim 1, wherein the mass ratio (A) / (B) of component (A) to component (B) is 0.005 to 0.
05.
3. One or more selected from (A) trimethylsiloxysilicic acid and its derivatives, (B) a hydrophobized colored pigment, and (C) an oil agent that is liquid at 25°C A slurry-like dispersion composed only of the above components.
4. One or more selected from (A) trimethylsiloxysilicic acid and its derivatives, (B) a hydrophobized colored pigment, and (C) an oil agent that is liquid at 25°C A cosmetic containing 1 to 30% by mass of the slurry-like dispersion, and (D) an organically modified clay mineral in an amount of 1.5% by mass or less.
5. The cosmetic according to Claim 4, wherein the slurry-like dispersion has a content of component (A) of 0.1 to 10% by mass, a content of component (B) of 20 to 89.9% by mass, and a content of component (C) of 10 to 40% by mass.
6. The cosmetic according to Claim 4 or 5, wherein component (C) is an oil agent that is liquid at 25°C and is selected from hydrocarbons and esters.
7. The cosmetic according to any one of Claims 4 to 6, wherein the mass ratio (A) / (B) of component (A) to component (B) is 0.005 to 0.
05.
8. The cosmetic according to any one of Claims 4 to 7, wherein the content of component (D) is 0.1 to 0.8% by mass in the whole cosmetic.
9. Step (I) of mixing one or more selected from (A) trimethylsiloxysilicic acid and its derivatives, (B) a hydrophobized colored pigment, and (C) an oil agent that is liquid at 25°C and selected from hydrocarbons and esters to prepare a slurry-like dispersion, Step (II-1) of mixing the obtained slurry-like dispersion with an oil phase component and then mixing an aqueous phase component into the obtained mixture II-1 A method for producing an oil-in-water type emulsified cosmetic having the above steps.
10. Step (I) of mixing one or more selected from (A) trimethylsiloxysilicic acid and its derivatives, (B) a hydrophobized colored pigment, and (C) an oil agent that is liquid at 25°C to prepare a slurry-like dispersion, A step (II-2) of mixing an oil phase component and an aqueous phase component, and mixing a slurry-like dispersion with the obtained mixture II-2 A method for producing an oil-in-water type emulsified cosmetic having the same.
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