Cosmetic

By integrating silicone polyurethane, an oil-soluble film-forming agent, and volatile oil in specific ratios, the cosmetic formulation achieves enhanced drying speed, uniformity, and durability, overcoming the challenges of maintaining shape and flexibility in eyelash cosmetics.

JP2025005436APending Publication Date: 2025-01-16KOSE CORPORATION

Patent Information

Application Number
JP2024103427
Authority / Receiving Office
JP · JP
Patent Type
Applications
Current Assignee / Owner
Priority Date
2023-06-27
Filing Date
2024-06-26
Publication Date
2025-01-16

AI Technical Summary

Technical Problem

Existing makeup technologies struggle to balance the need for a coating film that is both tough enough to maintain shape and flexible enough to withstand movement, while also ensuring uniformity, adhesion, and rapid drying, particularly in eyelash cosmetics.

Method used

Incorporating a specific silicone polyurethane, an oil-soluble film-forming agent, and a volatile oil into the cosmetic formulation, with precise mass ratios and components, to enhance the properties of the coating film.

Benefits of technology

The solution results in a cosmetic with improved drying speed, uniformity, makeup durability, and adhesion, addressing the limitations of previous technologies.

✦ Generated by Eureka AI based on patent content.

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Patent Text Reader

Abstract

To provide a cosmetic containing a specific silicone polyurethane, oil-soluble film-forming agent, and volatile oil, thereby exhibiting superior makeup endurance, uniformity of the coating layer, superior adhesion, and rapid drying of the coating layer.SOLUTION: The present invention relates to a cosmetic containing following components (A)-(C): a silicone polyurethane with a structural unit (1) based on a specific isocyanate compound, a structural unit (2) based on a specific dimethiconol, and a structural unit (3) based on a specific alkylene glycol, (B) an oil-soluble film-forming agent, and (C) a volatile oil.SELECTED DRAWING: None
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Description

[Technical field]

[0001] The present invention relates to a cosmetic preparation. [Background technology]

[0002] It is important for makeup products to maintain the finish they have immediately after application. To achieve long-lasting makeup, film-forming agents are often blended, and the coating properties must be both tough and flexible, as the products are used on moving areas such as the face and lips. For example, in the case of eye makeup cosmetics such as mascara, not only is a high level of toughness required for the coating film to fix the shape, etc. on the surfaces of the eyelids, eyelashes, and eyebrows, but flexibility is also required since they are exposed to blinking and movement more than 10,000 times a day. To date, various technical developments have been made for these products. In particular, in the case of mascara, for example, a cosmetic for eyelashes has been developed that contains a film-forming silicone compound, an organically modified clay mineral compound, a hydrophilic surfactant, and an aprotic polar solvent, and has a water content of 0.5% by mass or less, thereby providing curl retention, water resistance, and being easy to remove with warm water (see Patent Document 1). Also, a mascara has been developed that provides a makeup effect with good staying power over time, by using a mascara product that contains an aqueous medium and a film-forming polyurethane in the form of solid particles dispersed in the aqueous medium, has a viscosity in a specific range at a specific temperature and a specific shear rate, has a reservoir containing a wax-free composition, and has a sealing means with an applicator (see Patent Document 2). [Prior art documents] [Patent documents]

[0003] [Patent Document 1] JP 2017-132732 A [Patent Document 2] JP 2000-178137 A DISCLOSURE OF THEINVENTION [Problem to be solved by the invention]

[0004] However, in the technology of Patent Document 1, when trying to maintain the shape retention, i.e., curl retention and water resistance, the coating film formed is inflexible, and the coating film tends to crack over time. In addition, in the technology of Patent Document 2, the coating film is easily removed with water, especially warm water, and when an oil-soluble film former is added to this technology to improve water resistance, it is difficult to mix with water-dispersible polyurethane, and the film formation tends to be uneven. Therefore, it has been difficult to develop a cosmetic for eyelashes that satisfies high standards of coating film uniformity, adhesion, and drying speed. Therefore, the objective of the present invention is to develop a cosmetic that is excellent in all of the following: cosmetic durability, coating film uniformity, adhesion, and drying speed. [Means for solving the problem]

[0005] As a result of extensive research, the present inventors discovered that by containing a specific silicone polyurethane, an oil-soluble film-forming agent, and a volatile oil, a cosmetic composition can be obtained that exhibits excellent cosmetic durability, uniformity of the coating film, good adhesion, and drying speed of the coating film, and thus completed the present invention.

[0006] That is, the present invention provides: [1] The following components: (A) to (C); (A) The following formula (1) OCN-R 1 -NCO (1) (In the formula, R 1 represents an alkylene group having 2 to 9 carbon atoms. A structural unit based on an isocyanate compound represented by the formula: The following formula (2) [ka] (In the formula, n represents an integer of 1 to 100.) A structural unit based on dimethiconol represented by the formula: The following formula (3) H.O.R. 2 -OH (3) (In the formula, R 2 represents a linear or branched alkylene group having 2 to 9 carbon atoms which may have an ether bond. and a silicone polyurethane having a structural unit based on an alkylene glycol represented by the formula: (B) Oil-soluble film-forming agent (C) Volatile Oil The present invention relates to a cosmetic composition comprising the above-mentioned compound. [2] The present invention further relates to the cosmetic composition according to the above item [1], wherein the component (B) contains (B-1) a silicone-based resin. [3] The present invention further relates to the cosmetic preparation according to any one of the above [1] and [2], in which the mass ratio (B-1) / (B) of the component (B-1) to the component (B) is 0.3 to 1.0. [4] The cosmetic preparation according to any one of the above [1] and [2], wherein the content mass ratio (A) / (B) of the component (A) to the component (B) is 0.01 to 2.5. [5] The present invention relates to the cosmetic preparation according to either of the above [1] or [2], wherein the content of the component (A) is 0.1 to 10% by mass. [6] The present invention relates to the cosmetic preparation according to either [1] or [3] above, wherein the content of the component (B) is 1 to 25 mass %. [7] The present invention further relates to a cosmetic preparation according to either of the above [1] or [2], which contains component (D) a wax. [8] The present invention further relates to a cosmetic preparation according to either of the above [1] or [2], which contains a dextrin fatty acid ester as component (E). [9] Furthermore, the present invention relates to the cosmetic composition according to either of the above [1] or [2], wherein the cosmetic composition is an oil-based cosmetic composition or a water-in-oil cosmetic composition.

[10] Furthermore, the present invention relates to the cosmetic according to any one of [1] and [2] above, wherein the cosmetic is an eye makeup cosmetic.

[11] Furthermore, the present invention relates to the cosmetic composition according to either of the above [1] or [2], which is a hair cosmetic composition. Effect of the Invention

[0007] According to the present invention, it is possible to provide a cosmetic composition which is excellent in the drying speed of the coating film, the uniformity of the coating film, the cosmetic durability, and the adhesion. [Brief description of the drawings]

[0008] [Figure 1] This is a reference image taken from above after dissolving a part of Example 2 (Production Example 3 of component (A) + component (B) + component (C)) and a part of Comparative Example 1 (No. 5 raw material in Table 1 + component (B) + component (C)) at 90°C and cooling to room temperature. DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS

[0009] The present invention will be described in detail below. In this specification, the symbol "to" means a range including the numerical values ​​before and after it.

[0010] The silicone polyurethane of component (A) used in the present invention is represented by the following formula (1): OCN-R 1 -NCO (1) (In the formula, R 1 represents an alkylene group having 2 to 9 carbon atoms. A structural unit based on an isocyanate compound represented by the formula (hereinafter sometimes referred to as "isocyanate compound (1)"): The following formula (2) [ka] (In the formula, n represents an integer of 1 to 100.) A structural unit based on dimethiconol (hereinafter sometimes referred to as "dimethiconol (2)") represented by the formula: The following formula (3) H.O.R. 2 -OH (3) (In the formula, R2 represents a linear or branched alkylene group having 2 to 9 carbon atoms which may have an ether bond. and a structural unit based on an alkylene glycol represented by the following formula (hereinafter sometimes referred to as “alkylene glycol (3)”).

[0011] The component (A) used in the present invention has excellent compatibility with oils and can form a silicone polyurethane gel. The component (A) used in the present invention forms multiple ring-shaped clusters (clusters) by associating with each other at the hydrophilic parts in the molecule based on the alkylene glycol (3), and also exhibits a hydrophilic group associative thickening mechanism by contacting the oil with the hydrophobic parts in the molecule based on the isocyanate compound (1) and dimethiconol (2). It is presumed that the component (A) is gelled by finely taking three-dimensional structures based on this mechanism, and that the hydrophobic parts in the molecule impart flexibility and oil solubility, and that the polar groups in the hydrophilic parts in the molecule interact with each other to impart gelling power and restoring power. The component (A) used in the present invention is not water-soluble and separates from water when 5% silicone polyurethane and 95% water are heated to 80°C and stirred. Gelling oils include hydrocarbon oils, ester oils, oils and fats, silicone oils, fluorine-based oils, etc., regardless of the origin of the oil, such as animal oil, vegetable oil, or synthetic oil. Among these, silicone oils and hydrocarbon oils are preferred because they are highly compatible, form a gel with high elasticity and recovery, and further harden to produce a film with excellent flexibility and strength. Specifically, silicone oils include dimethylpolysiloxane, cyclomethicone, methylphenylpolysiloxane, diphenylpolysiloxane, methyltrimethicone, caprylylmethicone, trifluoropropylcyclotetrasiloxane, trifluoropropylcyclopentasiloxane, etc., and hydrocarbon oils include liquid paraffin, squalane, polybutene, polyisobutylene, undecane, tridecane, isododecane, (C13-15) alkanes, etc., and these can be used alone or in combination.

[0012] The structural unit of the component (A) used in the present invention is represented by the following formula (1): OCN-R 1 -NCO (1) In R 1 represents an alkylene group having 2 to 9 carbon atoms, which may be linear or branched, but is preferably linear. Examples of the alkylene group having 2 to 9 carbon atoms include ethylene, n-propylene, n-butylene, n-pentylene, and n-hexylene, and examples of the isocyanate compound represented by the above formula (1) include 1,4-tetramethylene diisocyanate, 1,5-pentamethylene diisocyanate, and 1,6-hexamethylene diisocyanate. Among these, 1,6-hexamethylene diisocyanate represented by the following formula (4) is preferred from the viewpoints of the elasticity and recovery of the gel formed and the flexibility of the film. [ka]

[0013] The structural unit of the component (A) used in the present invention is represented by the following formula (2): [ka] In dimethiconol represented by the formula: n is an integer of 1 to 100, and from the viewpoints of elasticity and recovery of the gel formed, flexibility of the film, etc., n is preferably 25 to 75, more preferably 40 to 75. The weight average molecular weight is not particularly limited, but from the viewpoints of elasticity and recovery of the gel formed, flexibility of the film, etc., it is preferably 1500 to 15000, more preferably 4000 to 11000, and even more preferably 6000 to 11000. In this specification, the weight average molecular weight means a value measured by gel permeation chromatography (GPC) (polystyrene equivalent value).

[0014] The structural unit of the component (A) used in the present invention is represented by the following formula (3): H.O.R. 2 -OH (3) In the alkylene glycol represented by the formula: 2represents a linear or branched alkylene group having 2 to 9 carbon atoms which may have an ether bond, and specific examples thereof include ethylene glycol, propylene glycol, 1,3-butylene glycol, 1,4-butylene glycol, diethylene glycol, triethylene glycol, dipropylene glycol, tripropylene glycol, etc. Among these, ethylene glycol represented by the following formula (5) is preferred from the viewpoints of the elasticity and recovery of the gel formed and the flexibility of the film. [ka]

[0015] The method for producing component (A) used in the present invention is not particularly limited, but examples thereof include a method in which an isocyanate compound (1) is reacted with dimethiconol (2) to obtain a polyurethane prepolymer represented by the following formula (6) (hereinafter sometimes referred to as "polyurethane prepolymer (6)"), and then this polyurethane prepolymer (6) is subjected to a polyaddition reaction with an alkylene glycol (3). [ka] In the above formula, R 1 and n are as defined above, R 1 represents an alkylene group having 2 to 9 carbon atoms, and n represents an integer of 1 to 100. In addition, m represents an integer of 1 to 7, and from the viewpoints of the elasticity and recovery of the formed gel and the flexibility of the film, it is preferably 1 to 3, and more preferably 1 or 2.

[0016] In reacting the isocyanate compound (1) with the dimethiconol (2) to obtain the polyurethane prepolymer (6), the molar ratio of the dimethiconol (2) to the isocyanate compound (1) (dimethiconol (2) / isocyanate compound (1)) is preferably 0.5 to 0.875, more preferably 0.5 to 0.75, and further preferably 0.5 to 0.67, from the viewpoints of the elasticity and recovery of the gel formed and the flexibility of the film. The weight average molecular weight of the urethane prepolymer is preferably 2,000 to 30,000, more preferably 4,000 to 20,000, and further preferably 4,000 to 15,000.

[0017] The component (A) used in the present invention represented by the following formula (7) is obtained by polymerizing the above polyurethane prepolymer (6) with alkylene glycol (3). The weight average molecular weight is preferably 10,000 to 300,000, more preferably 20,000 to 200,000, and even more preferably 30,000 to 100,000, from the viewpoints of the elasticity and recovery of the gel formed and the flexibility of the film. When the weight average molecular weight of the silicone polyurethane is less than 100,000, the molar ratio of dimethiconol (2) to alkylene glycol (3) (dimethiconol (2) / alkylene glycol (3)) is preferably 4 or less, more preferably 2 or less, and even more preferably 1 or less. On the other hand, when the weight average molecular weight of the silicone polyurethane is 100,000 or more, the molar ratio (dimethiconol (2) / alkylene glycol (3)) is preferably 6 or less, more preferably 4 or less, and even more preferably 2 or less, and the lower limit is preferably 1 or more. The most preferable combination of the weight average molecular weight and the molar ratio is a weight average molecular weight of 30,000 to 100,000, and a molar ratio of dimethiconol (2) to alkylene glycol (3) (dimethiconol (2) / alkylene glycol (3)) of 0.3 to 0.7. [ka] In the above formula, R 1 , R 2, n and m have the same meanings as above. r represents an integer of 1 to 3, preferably 1 or 2, and more preferably 1. s represents an integer of 1 to 50, preferably 2 to 10, and more preferably 5 to 10.

[0018] A preferred embodiment of the component (A) used in the present invention is exemplified by one represented by the following formula (8). [ka]

[0019] The component (A) used in the present invention can also be obtained by polymerizing an isocyanate compound (1), dimethiconol (2), and an alkylene glycol (3), followed by reaction with an alcohol. The alcohol is used to terminate the reaction, and is not particularly limited, but is preferably an alcohol having 2 to 10 carbon atoms, more preferably 2 carbon atoms. In this case, the molar ratio of each component may be the same as above.

[0020] The component (A) used in the present invention is, for example, Bis-Hydroxyethoxypropyl Dimethicone / Glycol / HDI Copolymer, as its INCI (International Nomenclature for Cosmetic ingredients) name, but is not particularly limited thereto.

[0021] As a method for producing the component (A), the silicone polyurethane gel can be obtained by polymerizing the silicone polyurethane in an oil agent or by mixing the silicone polyurethane and the oil agent in advance. For example, in the oil agent, an isocyanate compound (1) is reacted with a dimethiconol (2) to obtain a polyurethane prepolymer (6), and then the polyurethane prepolymer (6) is subjected to a polyaddition reaction with an alkylene glycol (3) to obtain a silicone polyurethane gel. The oil agent may be the component (C) described later or the gelling oil agent described above. Alternatively, a silicone polyurethane gel can be obtained by uniformly mixing dimethiconol (2) and alkylene glycol (3), and then adding an isocyanate compound (1) to cause a reaction.

[0022] The content of the component (A) used in the present invention as a solid content is not particularly limited, and is preferably 0.1 mass% (hereinafter simply abbreviated as %) or more, more preferably 0.3% or more, and even more preferably 1.0% based on the total amount of the cosmetic. Also, it is preferably 10% or less, more preferably 8%, and even more preferably 6% or less. Also, it is preferably 0.1 to 10%, more preferably 0.3 to 8%, and even more preferably 1.0 to 6%. This range is more preferable because it provides better coating film uniformity, cosmetic durability, and adhesion.

[0023] The oil-soluble film-forming agent of component (B) used in the present invention is soluble or dispersible in an oil agent to form a film. Here, forming a film means that a solution in which the resin is dissolved at 40% in a volatile solvent in which the resin is soluble is applied to a glass plate with a 400 μm thick applicator, and a continuous film is formed after drying at room temperature for 24 hours. The oil-soluble film-forming agent of component (B) used in the present invention is not particularly limited as long as it is one that can be used in ordinary cosmetics, and any one can be used. The component (B) oil-soluble film-forming agent is not particularly limited, but may be, for example, trimethylsiloxysilicate, polymethylsilsesquioxane, acrylic-silicone graft copolymer, silicone resin such as fluorine-modified silicone resin (hereinafter referred to as (B-1)), polyvinyl resin such as alkyl acrylate / vinyl acetate resin, alkyl acrylate / styrene resin, polyvinyl isobutyl ether, polybutene, polyisobutylene, rosin acid resin such as rosin modified phenol resin, rosin ester (e.g., hydrogenated rosin acid pentaerythrityl, etc.), hydrogenated abietic acid resin such as hydrogenated glyceryl abietic acid, candelilla resin, carnauba extract, etc., and one or more of these oil-soluble resins may be used. Among them, one or more of the silicone resins (B-1) are preferably selected. Furthermore, it is preferable for ease of handling that the solution or dispersion is diluted with a solvent, or that the solution or dispersion is obtained by mixing in advance. As the solvent for diluting or dispersing the component (B), one or more selected from dimethicone, octamethylcyclotetrasiloxane, decamethylcyclopentasiloxane, hydrogenated polyisobutene, and isododecane are preferable, and volatile dimethicone and isododecane are more preferable. In addition, volatile means that the flash point is 35 to 90°C. Commercially available products dissolved in these volatile oils can also be used.

[0024] Commercially available products of the component (B) oil-soluble film-forming agent in the present invention include, for example, (B-1) silicone resins, such as trimethylsiloxysilicate, Silicon X-21-5250 (50% decamethylcyclopentasiloxane solution), Silicon X-21-5250L (50% volatile dimethicone solution), KF-7312T (60% methyltrimethicone solution), KF-7312J (50% decamethylcyclopentasiloxane solution), KF-7312K (60% dimethicone solution), KF-9021 (50 % decamethylcyclopentasiloxane solution), KF-9021L (50% volatile dimethicone solution) (all manufactured by Shin-Etsu Chemical Co., Ltd.), BY11-018 (30% solid content cyclopentasiloxane solution, manufactured by Toray Dow Corning Co., Ltd.), SS4267 (35% dimethicone solution), SILSOFT74 (75% isododecane solution) (manufactured by Momentive Performance Materials Japan Co., Ltd.), SR-1000 (100% solid content: manufactured by Momentive Performance Materials Co., Ltd.), etc. Examples of polymethylsilsesquioxane include SILFORM FLEXIBLE RESIN (100% solid content) (manufactured by Momentive Performance Materials Japan Co., Ltd.), BELSIL PMS MK POWDER SILICONE RESIN (100% solid content) (Asahi Kasei Wacker Silicone), etc. Examples of the acrylic-silicone graft copolymer include (acrylates / dimethicone) copolymer, (acrylates / stearyl acrylate / dimethicone methacrylate) copolymer, (acrylates / ethylhexyl acrylate / dimethicone methacrylate) copolymer, (acrylates / behenyl acrylate / dimethicone methacrylate) copolymer, etc. Commercially available products include KP-540, KP541, KP-545L, KP-550, KP-545, KP-562, KP-561P (manufactured by Shin-Etsu Chemical Co., Ltd.), etc. Examples of silicone-based resins such as fluorine-modified silicone resins include XS66-B8226 (solid content 50%, solvent: cyclopentasiloxane, manufactured by Momentive Performance Materials, Inc.), etc. In addition, the other resin may be one extracted from a natural product or one synthesized, and is not particularly limited as long as it is a polymer that forms a film.Specifically, as the extract from a natural product, ester resins include Candelilla resin E-1, E-2 (manufactured by Nippon Natural Products Co., Ltd.), TOWAX-1B4 (manufactured by Toa Kasei Co., Ltd.), Ester Gum HP (manufactured by Arakawa Chemical Industries Co., Ltd.), Pine Crystal KE-311 (manufactured by Arakawa Chemical Industries Co., Ltd.), etc.

[0025] The content of component (B) in the present invention is not particularly limited, and is preferably 1% or more, more preferably 2% or more, and even more preferably 3% or more, based on the total amount of the cosmetic. It is also preferably 25% or less, and more preferably 20% or less. It is also preferably 1 to 25%, more preferably 2 to 20%, and even more preferably 3 to 15%. This range is more preferable because it provides better drying speed of the coating film, uniformity of the coating film, and cosmetic durability. The mass ratio (B-1) / (B) of the component (B-1) in the component (B) is not particularly limited, but the lower limit is preferably 0.1 or more, more preferably 0.2 or more, and even more preferably 0.3 or more. The upper limit is 1.0 or less. The range is preferably 0.1 to 1.0, more preferably 0.2 to 1.0, and even more preferably 0.3 to 1.0. This range is more preferable because it provides better drying speed and uniformity of the coating film.

[0026] In the present invention, the mass ratio (A) / (B) of component (A) to component (B) is not particularly limited, but is preferably 0.01 or more, more preferably 0.05 or more, and even more preferably 0.1 or more. It is preferably 2.5 or less, more preferably 1.0 or less, and even more preferably 0.8 or less. It is preferably 0.01 to 2.5, more preferably 0.05 to 1.0, and even more preferably 0.1 to 0.8. This range is preferable in terms of excellent coating film uniformity, cosmetic durability, and coating film uniformity.

[0027] The component (C) volatile oil used in the present invention is an oil agent that is volatile at 20°C and normal pressure. Here, volatile means that the boiling point at normal pressure (1 atm) is 260°C or less. The component (C) volatile oil is not particularly limited, but examples thereof include volatile silicone oil, volatile hydrocarbon oil, volatile polar solvent, etc., and one or more of these can be used. Among these, silicone oil and hydrocarbon oil are preferred from the viewpoint of the drying speed of the coating film, and hydrocarbon oil is more preferred.

[0028] The volatile silicone oil of component (C) used in the present invention is not particularly limited, but examples thereof include dimethylpolysiloxane, methyltrimethicone, octamethylcyclotetrasiloxane, decamethylcyclopentasiloxane, dodecamethylcyclohexasiloxane, etc., which are generally used in cosmetics. Commercially available products include DC345 FLUID, SH245 FLUID (manufactured by Toray Dow Corning Co., Ltd.), KF-995, TMF1.5, Silicone KF-96L-1.5CS, KF-96L-2CS (all manufactured by Shin-Etsu Chemical Co., Ltd.), BELSIL DM 1 PLUS (manufactured by Wacker Chemical Corporation), etc. These volatile silicone oils may be used alone or in combination of two or more. As the volatile silicone oil, those with a boiling point of less than 200°C are preferred in terms of drying speed, and for example, methyltrimethicone and dimethicone are preferably used.

[0029] The volatile hydrocarbon oil, component (C), used in the present invention is not particularly limited, but examples thereof include paraffinic hydrocarbon oils such as n-heptane, n-decane, n-undecane, and n-dodecane; and isoparaffinic hydrocarbon oils such as isodecane, isododecane, and hydrogenated polyisobutene. These may be used alone or in combination of two or more. Commercially available products include MARUKAZOL R (Maruzen Petrochemical Co., Ltd.), CETIOL (registered trademark) ULTIMATE (BASF Japan Ltd.), ARLAMOL HD (Croda Japan), IP Solvent 1620, IP Solvent 2028 (all manufactured by Idemitsu Petrochemical Co., Ltd.), DEDRAFLOW 5 (CIT), PERMETHYL 99A (PRESPERS), AEC Isododecane (A and E Connock (Perfumery and Cosmetics) Ltd.), Creasil ID CG (CIT Sarl), Fancol ID (Elementis Specialties), Orister IDD (Orient Stars LLC), Permethyl 99A (Presperse Corp), ISODODECANE (IMCD INEOS Oligomers), and Ritacane ID (Rita Corporation). Among these, from the viewpoints of smooth spreading and an appropriate film-forming rate of the cosmetic film, one or more types selected from the group consisting of isododecane and undecane / tridecane are preferred, and it is even more preferred that the volatile hydrocarbon oil is isododecane. Examples of the volatile polar solvent include ethyl acetate, butyl acetate, propylene carbonate, acetone, and butanol.

[0030] The content of component (C) in the present invention is not particularly limited, and is preferably 10% or more, more preferably 15% or more, and even more preferably 20% or more, based on the total amount of the cosmetic. It is also preferably 80% or less, more preferably 70% or less, and even more preferably 65% ​​or less. It is also preferably 10 to 80%, more preferably 15 to 70%, and even more preferably 20 to 65%. This range is more preferable because it provides a superior drying speed of the coating film.

[0031] The cosmetic of the present invention may further contain a wax component (D). Any wax that is normally used in cosmetic compositions may be used. For example, waxes such as hydrocarbon wax, ester wax, oils and fats, silicone wax, etc. include hydrocarbon waxes such as paraffin wax, ceresin wax, montan wax, microcrystalline wax, synthetic wax, ethylene-propylene copolymer, polyethylene wax, Fischer-Tropsch wax, ozokerite wax, hydrogenated microcrystalline wax, (ethylene / propylene) copolymer, etc., ester waxes such as candelilla wax, carnauba wax, beeswax, rice wax, sunflower wax, jojoba ester, shea butter, cacao butter, coconut oil, hardened coconut oil, mango butter, Japan wax kernel oil, hardened oil, rice bran wax, beeswax, etc., and further silicone waxes such as (eicosene / vinylpyrrolidone) copolymer, long-chain alkoxy-modified silicone, long-chain alkyl-modified silicone (e.g., stearyl dimethicone, etc.), etc., and one or more of these may be used.

[0032] Among these, from the viewpoints of cosmetic durability and adhesion, one or more selected from the group consisting of polyethylene wax, paraffin wax, microcrystalline wax, Fischer-Tropsch wax, candelilla wax, carnauba wax, shea butter, beeswax, (ethylene / propylene) copolymer, and stearyl dimethicone are more preferred, and one or more selected from the group consisting of polyethylene wax, paraffin wax, microcrystalline wax, candelilla wax, carnauba wax, shea butter, beeswax, and stearyl dimethicone are even more preferred.

[0033] The content of component (D) in the present invention is not particularly limited, and is preferably 0.1% or more, more preferably 0.3% or more, and even more preferably 0.5% or more, based on the total amount of the cosmetic. It is also preferably 15% or less, more preferably 12% or less, and even more preferably 10% or less. It is also preferably 0.1 to 15%, more preferably 0.3 to 12%, and even more preferably 0.5 to 10. This range is more preferable because it provides better drying speed, cosmetic durability, and adhesion of the coating film.

[0034] The cosmetic of the present invention may further contain a component (E) dextrin fatty acid ester. Component (E) is an ester of a fatty acid and dextrin. In the present invention, the fatty acid may be a linear or branched, saturated or unsaturated fatty acid. The fatty acid is not particularly limited, but the number of carbon atoms of the fatty acid is preferably 8 to 22, more preferably 12 to 18, and even more preferably 14 to 18. Examples of such fatty acids include, but are not particularly limited to, ethylhexanoic acid, caprylic acid, capric acid, lauric acid, myristic acid, palmitic acid, stearic acid, isostearic acid, oleic acid, linoleic acid, linolenic acid, behenic acid, etc., and one or more of these may be used. Examples of dextrin fatty acid esters include dextrin myristate, dextrin palmitate, dextrin (palmitate / 2-ethylhexanoate), dextrin stearate, dextrin isostearate, and dextrin oleate, and one or more of these can be used. In addition, it is preferable that the proportion of branched fatty acids in the fatty acids substituted on the dextrin is less than 50%. This is more preferable because it provides better coating uniformity.

[0035] The dextrin fatty acid ester of component (E) in the present invention is preferably an ester of a fatty acid having 8 to 22 carbon atoms with dextrin, more preferably one or more selected from the group consisting of dextrin myristate, dextrin palmitate, and (palmitic acid / 2-ethylhexanoic acid) dextrin, and dextrin isostearate, even more preferably one or two selected from the group consisting of dextrin myristate and dextrin palmitate, and most preferably dextrin palmitate.

[0036] The content of component (E) in the present invention is not particularly limited, and is preferably 0.1% or more, more preferably 0.5% or more, and even more preferably 1.0% or more, based on the total amount of the cosmetic. It is also preferably 5.0% or less, more preferably 4.5% or less, and even more preferably 4.0% or less. It is also preferably 0.1 to 5.0%, more preferably 0.5 to 4.5%, and even more preferably 1.0 to 4.0%. This range is more preferable because it provides better uniformity of the coating film.

[0037] The cosmetic of the present invention may contain components used in ordinary cosmetic preparations as necessary, within the scope of not impairing the effects of the present invention, such as polymers other than component (A), oily components other than components (B), (C), (D), and (E), surfactants, aqueous components, UV absorbers, moisturizers, antioxidants, anti-fading agents, preservatives, medicinal ingredients, stabilizers, pigments, fragrances, etc.

[0038] The cosmetic preparation of the present invention can be produced by a conventional method, for example, by heating components (A), (B), (C), and, if necessary, components (D), (E), and optional components to a temperature equal to or higher than the melting point of component (A) (e.g., 90°C), and then mixing them.

[0039] The cosmetic of the present invention is not particularly limited in its formulation or application site, and can be used to produce cosmetics in various formulations, such as liquid, emulsion, cream, solid, paste, gel, powder, press, multi-layer, mousse, spray, or stick form, and can also be used to produce cosmetics intended for various application sites, such as makeup cosmetics, skin care cosmetics, hair cosmetics, antiperspirants, or UV protection cosmetics. The cosmetic can be an oil-based type, oil-in-water type, water-in-oil type, or a multiphase emulsion type that is a combination of these, but from the viewpoints of cosmetic durability, uniformity of the coating film, etc., oil-based and water-in-oil types are preferred, and oil-based cosmetics are particularly preferred.

[0040] The cosmetic product of the present invention is not limited as a cosmetic item, and examples thereof include basic cosmetics such as lotion, milky lotion, beauty essence, pack, all-in-one gel, cream, body milk, oil cleansing, cleansing cream, and sunscreen, hair cosmetics such as styling water and hair wax, and makeup cosmetics such as mascara, lip gloss, lipstick, eyeshadow, eyeliner, foundation, face color, concealer, makeup base, and body tattoo. Although not particularly limited, the cosmetic product can be preferably used for eye makeup cosmetics such as mascara, eyelash base, mascara overcoat, eyeliner, and eyebrow, or for the purpose of applying to hair, such as mascara, eyelash base, mascara overcoat, eyebrow, and hair cosmetics.

[0041] The present invention can also have the following configuration.

[12] The cosmetic preparation according to the above item [3], wherein the mass ratio (A) / (B) of the component (A) to the component (B) is 0.01 to 2.5.

[13] The cosmetic preparation according to the above item

[12] , wherein the content of the component (A) is 0.1 to 10 mass %.

[14] The cosmetic preparation according to any one of

[12] and

[13] above, wherein the content of the component (B) is 1 to 25 mass %.

[15] The present invention further relates to the cosmetic preparation according to any one of

[12] to

[14] above, which further contains a component (D) wax.

[16] The present invention further relates to the cosmetic preparation according to any one of the above

[12] to

[15] , which further contains a dextrin fatty acid ester as a component (E).

[17] The present invention further relates to the cosmetic composition according to any one of the above

[12] to

[16] , wherein the cosmetic composition is an oil-based cosmetic composition or a water-in-oil cosmetic composition.

[18] The present invention further relates to the cosmetic composition according to any one of

[12] to

[16] above, which is a hair cosmetic composition.

[0042] The present invention will be described in more detail below with reference to examples, but the present invention is not limited to these examples.

[0043] [Production Example 1 of Component (A)] (Containing Component (C) Dimethicone (2cs)) A 3 L three-neck flask was charged with 201 parts of dimethiconol (molecular weight approximately 2000, quantitative value based on terminal hydroxyl value; weight average molecular weight approximately 4000), 30 parts of dimethicone (2cs), and 33 parts of hexamethylene diisocyanate, and mixed uniformly. While controlling the temperature at 70° C., 0.025 parts of dibutyltin dilaurate was added, and after stirring for 2 hours, 6 parts of ethylene glycol was added. After the addition was completed, the mixture was stirred at 70° C. for 16 hours, and then 0.5 parts of ethanol and 40 parts of dimethicone (2cs) were added to complete the reaction. The weight average molecular weight of the silicone polyurethane in the obtained silicone polyurethane gel was 38,000 as determined by GPC measurement (polystyrene equivalent).

[0044] [Production Example 2 of Component (A)] (Containing Component (C) Dimethicone (2cs)) A 3 L three-neck flask was charged with 214 parts of dimethiconol (molecular weight approximately 5000, quantitative value based on terminal hydroxyl value; weight average molecular weight approximately 11000), 30 parts of dimethicone (2cs), and 20 parts of hexamethylene diisocyanate, and mixed uniformly. While controlling the temperature at 70° C., 0.025 parts of dibutyltin dilaurate was added, and after stirring for 2 hours, 6 parts of ethylene glycol was added. After the addition was completed, the mixture was stirred at 70° C. for 16 hours, and then 0.5 parts of ethanol and 40 parts of dimethicone (2cs) were added to complete the reaction. The weight average molecular weight of the silicone polyurethane in the obtained silicone polyurethane gel was 29,446 as determined by GPC (polystyrene equivalent).

[0045] [Production Example 3 of Component (A)] (Containing Component (C) Dimethicone (2cs)) A 3 L three-neck flask was charged with 212 parts of dimethiconol (molecular weight approximately 5000, quantitative value based on terminal hydroxyl value; weight average molecular weight approximately 11000), 30 parts of dimethicone (2cs), and 21 parts of hexamethylene diisocyanate, and mixed uniformly. While controlling the temperature at 70° C., 70 parts of dibutyltin dilaurate was added, and after stirring for 2 hours, 6 parts of ethylene glycol was added. After the addition was completed, the mixture was stirred at 70° C. for 16 hours, and then 0.5 parts of ethanol and 40 parts of cyclomethicone were added to complete the reaction. The weight average molecular weight of the silicone polyurethane in the obtained silicone polyurethane gel was 63,793 as determined by GPC measurement (polystyrene equivalent).

[0046] [Production Example 4 of Component (A)] (Containing Component (C) Dimethicone (6cs)) A 3 L three-neck flask was charged with 214 parts of dimethiconol (molecular weight approximately 5000, quantitative value based on terminal hydroxyl value; weight average molecular weight approximately 11000), 30 parts of dimethicone (6cs), and 20 parts of hexamethylene diisocyanate, and mixed uniformly. While controlling the temperature at 70° C., 0.025 parts of dibutyltin dilaurate was added, and after stirring for 2 hours, 6 parts of ethylene glycol was added. After the addition was completed, the mixture was stirred at 70° C. for 16 hours, and then 0.5 parts of ethanol and 40 parts of dimethicone (6cs) were added to complete the reaction. The weight average molecular weight of the silicone polyurethane in the obtained silicone polyurethane gel was 57,419 as determined by GPC measurement (polystyrene equivalent).

[0047] [Production Example 5 of Component (A)] (Containing Component (C) Dimethicone (2cs)) A 3 L three-neck flask was charged with 220 parts of dimethiconol (molecular weight approximately 3000, quantitative value based on terminal hydroxyl value; weight average molecular weight approximately 6000), 30 parts of dimethicone (2cs), and 18 parts of hexamethylene diisocyanate, and mixed uniformly. While controlling the temperature at 70° C., 0.025 parts of dibutyltin dilaurate was added, and after stirring for 2 hours, 2 parts of ethylene glycol was added. After the addition was completed, the mixture was stirred at 70° C. for 16 hours, and then 0.5 parts of ethanol and 40 parts of dimethicone (2cs) were added to complete the reaction. The weight average molecular weight of the silicone polyurethane in the obtained silicone polyurethane gel was 299,825 as determined by GPC measurement (polystyrene equivalent).

[0048] [Comparative Manufacturing Example 1 of Component (A)] (Containing Component (C) Dimethicone (2cs)) A 3 L three-neck flask was charged with 345 parts of dimethiconol (molecular weight approximately 5000, quantitative value based on terminal hydroxyl value. Weight average molecular weight approximately 11000), 345 parts of polyethylene glycol (molecular weight approximately 4000, quantitative value based on terminal hydroxyl value. Weight average molecular weight approximately 6000), 30 parts of dimethicone (2cs), and 20 parts of hexamethylene diisocyanate, and mixed uniformly. While controlling the temperature at 70° C., 0.025 parts of dibutyltin dilaurate was added, and after stirring at 70° C. for 16 hours, 0.5 parts of ethanol and 40 parts of dimethicone (2cs) were added to complete the reaction. The weight average molecular weight of the silicone polyurethane in the obtained silicone polyurethane gel was 60,000 as determined by GPC measurement (polystyrene equivalent).

[0049] Examples 1 to 22 and Comparative Examples 1 to 5: Oil-based and water-in-oil eyelash cosmetics Oil-based and water-in-oil eyelash cosmetics having the formulations shown in Tables 1 to 3 were prepared by the manufacturing method described below, and (a) the drying speed of the coating film, (b) the uniformity of the coating film, (c) the cosmetic durability, and (d) the adhesion were evaluated by the evaluation methods described below. The results are also shown in Tables 1 to 3.

[0050] [Table 1] *1: Leopearl KL2 (manufactured by Chiba Flour Mills) *2: TOWAX-1F6 (manufactured by Toa Kasei Co., Ltd.) *3: ISODODECANE (manufactured by INEOS Oligomers) *5: SR1000 (Momentive Performance Materials Japan) *10: J-Lecithin CL (Lecithin CLO) (manufactured by J-Oil Mills) *11: Hi-Filler K-5 (Matsumura Sangyo Co., Ltd.) *12: AEROSIL 380S (manufactured by Nippon Aerosil Co., Ltd.)

[0051] [Table 2] *4: BELSIL DM 1 PLUS (Asahi Kasei Wacker Silicone) *6: SILFORM FLEXIBLE RESIN (manufactured by Momentive Performance Materials Japan) *7: KP-550 (40% solids, isododecane solvent) (manufactured by Shin-Etsu Chemical Co., Ltd.) *8: Estergum HP (manufactured by Arakawa Chemical Industries, Ltd.)

[0052] [Table 3] *9:CITHROL DPHS-SO-(JP) (manufactured by Croda Japan)

[0053] (Manufacturing method) (Contains only the ingredients with the listed No.) A. Heat ingredients (1) to (9) to 100°C and mix uniformly. Components (10)-(17) and uniformly dispersed components (20)-(25) are added to the BA and uniformly dispersed at room temperature, after which components (18) and (19) are added and mixed last. CB was filled into a container equipped with an applicator (nylon brush) to obtain oil-based and water-in-oil type eyelash cosmetics.

[0054] <Evaluation method> Each sample was evaluated and judged for the following evaluation items (a) to (d) by the following methods. <Evaluation items> (a) Drying speed of the coating (b) Uniformity of coating film (C) Makeup retention (D) Adhesion

[0055] For the evaluation items (i) to (iv), a use test was conducted for each sample by a panel of 10 cosmetic evaluation specialists, who each evaluated and scored the sample on a 6-7 scale using the absolute evaluation criteria below. The average score of each sample given by all panelists was then calculated, and the sample was judged according to the 5-stage judgment criteria below.

[0056] (Evaluation items and evaluation criteria) The following evaluation items were evaluated by the following methods. Evaluation item (a): The drying speed of the coating was measured by applying each sample to the skin or hair, and then measuring the time it took for the sample to disappear when lightly touched with a finger. The drying speed was evaluated according to the following criteria. (Judgment): (Evaluation criteria) 6: Dries in less than a minute 5: Dries in 1 minute or more but less than 2 minutes 4: Dries in 2 to 3 minutes 3: Dries in 3 minutes or more but less than 4 minutes 2: Dry in 4 minutes or more but less than 5 minutes 1: It takes more than 5 minutes to dry (5-level rating scale) (Judgment): (Average score) AA: Over 5.5 points: Best A: More than 5 points, 5.5 points or less: Very good B: 3.5 points or more and 5 points or less: Good C: More than 2 points and 3.5 points or less: slightly poor D: 2 points or less: Defective

[0057] Evaluation item (b): Regarding the uniformity of the coating, each sample was applied to the skin or hair and visually evaluated to see whether the sample was uneven or lumpy. (Absolute evaluation criteria) (Score):(Evaluation) 6: Very good, no unevenness or lumps 5: Good, no unevenness or lumps 4: Good, with no unevenness or lumps 3: Neither 2: Somewhat uneven and lumpy, poor quality 1: Bad, uneven and lumpy 0: Very uneven and lumpy, poor quality (5-level rating scale) (Judgment): (Average score) AA: Over 5.5 points: Best A: More than 5 points, 5.5 points or less: Very good B: 3.5 points or more and 5 points or less: Good C: More than 2 points and 3.5 points or less: slightly poor D: 2 points or less: Defective FIG. 1 shows an image of a part of Example 2 (a mixture of component (A) Production Example 3 + (C) isododecane*3 + (B) trimethylsiloxysilicate*5) dissolved, and a similar image of a part of Comparative Example 1. By improving the dispersibility of components (A) to (C), the uniformity of the coating film tends to increase.

[0058] Evaluation item (c): Regarding makeup durability, each sample was applied to the skin or hair, and the extent to which the coating film had changed six hours later was visually evaluated in comparison to immediately after application. (Absolute evaluation criteria) (Score):(Evaluation) 6: The shape and makeup film are well maintained 5: The shape and cosmetic film are well maintained 4: Fairly good 3: Neither 2: The shape and makeup film are not maintained well. 1: The shape and makeup film are not maintained well. 0: The shape and makeup film are not maintained very well. (5-level rating scale) (Judgment): (Average score) AA: Over 5.5 points: Best A: More than 5 points, 5.5 points or less: Very good B: 3.5 points or more and 5 points or less: Good C: More than 2 points and 3.5 points or less: slightly poor D: 2 points or less: Defective

[0059] Evaluation item (ii): Adhesion was evaluated visually after applying each sample to the skin or hair. In particular, in the case of hair cosmetics, the samples were applied to hair and the effect of increasing volume due to adhesion was evaluated visually. (Absolute evaluation criteria) (Score):(Evaluation) 6: Very good adhesion 5: It's okay to stick 4: Some adhesion is good 3: Neither 2: Slightly poor adhesion 1: Poor adhesion 0: Very poor adhesion (5-level rating scale) (Judgment): (Average score) AA: Over 5.5 points: Best A: More than 5 points, 5.5 points or less: Very good B: 3.5 points or more and 5 points or less: Good C: More than 2 points and 3.5 points or less: slightly poor D: 2 points or less: Defective

[0060] As is clear from the results in Table 1, the oil-based eyelash cosmetics of Examples 1 to 18 and Examples 20 to 22 of the present invention and the water-in-oil eyelash cosmetics of Example 19 were excellent in drying speed of the coating film, uniformity of the coating film, cosmetic durability, and adhesion. On the other hand, Comparative Example 1, which contained a (hydrogenated polybutadiene / glycol / HDI) copolymer instead of component (A), did not provide satisfactory quality in terms of the drying speed of the coating film, the uniformity of the coating film, and cosmetic durability. Comparative Example 2, which did not contain component (A), did not provide satisfactory quality in terms of coating film uniformity, cosmetic durability, and adhesion. Comparative Example 3, which contained Comparative Production Example 1 instead of component (A), did not provide satisfactory quality in terms of coating film uniformity, cosmetic durability, and drying speed. Comparative Example 4, which did not contain component (B), did not provide satisfactory quality in terms of drying speed of the coating film, uniformity of the coating film, cosmetic durability, and adhesion. Comparative Example 5, which did not contain component (C), did not provide satisfactory quality in terms of drying speed of the coating film, uniformity of the coating film, cosmetic durability, and adhesion.

[0061] Example 23: Oil-based mascara (Component) (%) (1) Candelilla wax *13 3 (2) Beeswax 2 (3) Carnauba wax *2 2 (4) Polyethylene wax 1 (5) Polymethylsilsesquioxane *6 2 (6) Trimethylsiloxysilicate *5 10 (7) Dextrin isostearate *15 2 (8) Candelilla wax extract *16 1 (9) Silicone polyurethane gel composition of Production Example 1 of component (A) (30% 2CS solvent) 5 (10) Dimethiconol 2 (11) Dextrin palmitate *14 4 (12) Isododecane remaining (13) Silica anhydride *12 1.5 (14) Black iron oxide 2 (15) Carmine 2 (16) Rayon fiber (fiber diameter 7D, fiber length 2mm) 2 (17) Nylon fiber (fiber diameter 4T, fiber length 2mm) 0.5 (18) Polypropylene fiber (fiber diameter 5.6D, fiber length 2 mm) 0.5 *13: Refined Candelilla Wax SR-3 (manufactured by Nippon Natural Products) *14: Leopearl TL2 (manufactured by Chiba Flour Mills) *15: Unifilma HVY (manufactured by Chiba Flour Mills) *16: Candelilla resin E-1 (manufactured by Nippon Natural Products Co., Ltd.)

[0062] (Manufacturing method) A. Heat ingredients (1) to (12) to 100°C and mix uniformly. Components (13) to (18) are added to the BA and dispersed uniformly at room temperature. The CB is filled into a container with an applicator (nylon brush) to make the product.

[0063] The oil-based mascara of the present invention was excellent in drying speed, uniformity, cosmetic durability and adhesion.

[0064] Example 24: Oil-based eyeliner (Component) (%) (1) Isododecane *3 remaining (2) Silicone polyurethane gel composition of Production Example 3 of component (A) (30% 2CS solvent) 4 (3) Candelilla wax *13 3 (4) Paraffin 1 (5) Trimethylsiloxysilicate *5 12 (6) (Acrylates / Dimethicone) Copolymer *7 (Solids content 40% isododecane solution) 8 (7) Dextrin palmitate *1 2 (8) Sorbitan sesquioleate 0.5 (9) Lecithin *10 0.3 (10) Disteardimonium hectorite *17 3 (11) Propylene carbonate 0.5 (12) Black iron oxide 10 (13) Carbon black 5 (14) Silylated anhydrous silica*18 1 (15) Titanium Mica 3 (16) Titanium oxide coated glass powder *19 2 *17: BENTONE 38V BC (manufactured by Elementis) *18: AEROSIL R972 (manufactured by Nippon Aerosil Co., Ltd.) *19: Metashine MT1080RR (manufactured by Nippon Sheet Glass Co., Ltd.)

[0065] (Manufacturing method) A. Heat ingredients (1) to (11) to 100°C and mix uniformly. Add components (12) to (16) in BA and disperse uniformly at room temperature. The CB is filled into containers to produce the product.

[0066] The oil-based eyeliner of the present invention was excellent in drying speed, uniformity, cosmetic durability and adhesion.

[0067] Example 25: Oily eyebrows (Component) (%) (1) Isododecane *3 remaining (2) Silicone polyurethane gel composition of Production Example 2 of component (A) (30% 2CS solvent) 3 (3) Carnauba wax *2 2 (4) Microcrystalline wax 1 (5) Stearyl dimethicone *20 1 (6) Trimethylsiloxysilicate *5 3 (7) Polymethylsilsesquioxane *6 2 (8) Hydrogenated glyceryl abietic acid *21 2 (9) Dextrin isostearate*15 0.5 (10) Dextrin palmitate *14 3 (11) Disteardimonium hectorite *17 3 (12) Propylene carbonate 0.5 (13) Black iron oxide 3 (14) Red iron oxide 1 (15) Yellow iron oxide 2 (16) Titanium dioxide 0.5 (17) Talc *11 5 (18) Methyl methacrylate crosspolymer *22 1 (19) Silica 1 (20) Cellulose 1 *20: 2503 Cosmetic Wax (Dow Corning Toray Co., Ltd.) *21: Pine Crystal KE-311 (manufactured by Arakawa Chemical Industries) *22: Ganz Pearl GM-2800 (manufactured by Aica Kogyo Co., Ltd.)

[0068] (Manufacturing method) A. Heat ingredients (1) to (12) to 100°C and mix uniformly. Add components (13) to (20) in BA and disperse uniformly at room temperature. The CB is filled into containers to produce the product.

[0069] The oily eyebrow product of the present invention was excellent in drying speed, uniformity, cosmetic durability, and adhesion.

[0070] Example 26: Oil-based mascara base (Component) (%) (1) Isododecane *3 remaining (2) Silicone polyurethane gel composition of Production Example 5 of component (A) (30% 2CS solvent) 6 (3) Dimethicone *4 2 (4) Carnauba wax *2 0.5 (5) Dextrin palmitate *1 3 (6) Quaternium-18 Hectorite *23 3 (7) Propylene carbonate 0.5 (8) Trimethylsiloxysilicate *5 7 (9) Polymethylsilsesquioxane *6 4 (10) Hydrogenated glyceryl abietic acid *21 2 (11) Fumed silica *12 1 *23: Sumecton SAN-P (Kunimine Industries)

[0071] (Manufacturing method) A. Heat ingredients (1) to (10) to 100°C and mix uniformly. Add component (11) to the BA and disperse uniformly at room temperature. The CB is filled into a container with an applicator (nylon brush) to make the product.

[0072] The oil-based mascara base of the present invention was excellent in drying speed, uniformity, makeup durability and adhesion of the coating.

[0073] Example 27: Water-in-oil BB cream (Can be used as a sunscreen, primer, foundation, concealer and lotion) A water-in-oil BB cream was prepared according to the composition and manufacturing method shown below. (Component) (%) (1) Isododecane *3 4 (2) Undecane / Tridecane 4 (3) Lauryl PEG-9 Polydimethylsiloxyethyl Dimethicone 0.8 (4) PEG-9 Polydimethylsiloxyethyl Dimethicone 0.4 (5) Sorbitan sesquiisostearate 0.6 (6) Neopentyl glycol diethylhexanoate 10 (7) Octyl palmitate 3 (8) Silicone polyurethane gel composition of Production Example 4 of component (A) (30% 6CS solvent) 2 (9) (Acrylates / Dimethicone) Copolymer *7 (Solids content 40% isododecane solution) 2 (10) Titanium dioxide treated with 3% disodium N-stearoyl-L-glutamate (average particle size 270 nm) 9 (11) Fine particle titanium dioxide (average particle diameter 35 nm) treated with 3% aluminum hydroxide, 5.5% hydrated silica, and 3% zinc laurate 7 (12) Pigment-grade titanium dioxide treated with 3% zinc laurate (Average particle size 250nm) 1 (13) Black iron oxide treated with 2Na stearoyl glutamate 3% 0.2 (14) Red iron oxide treated with 2Na stearoyl glutamate 3% 0.3 (15) Yellow iron oxide treated with 2Na stearoyl glutamate 3% 0.6 (16) Hydrogenated lecithin *24 0.5 (17) Dimethyl distearyl ammonium hectorite 1.5 (18) Benzyl dimethylstearyl ammonium hectorite 0.6 (19) Polyglyceryl-6 polyricinoleate (HLB 3.3) 2 (20) Ethylhexyl methoxycinnamate 6 (21) 2-(4-Diethylamino-2-hydroxybenzoyl)benzoic acid hexyl ester 2 (22) Spherical silica *26 5 (23) Titanium mica (average particle size 15 μm) 5 (24) Talc*11 5 (25) Remaining purified water (26) Ethanol 5 (27) Tripropylene glycol 10 (28) 1,3-Butylene glycol 10 *24: Resinol S-10E (manufactured by Nikko Chemicals)

[0074] (Manufacturing method) A: Heat ingredients (6) to (8) to 80°C and mix and dissolve uniformly. B: Components (10) to (16) and a portion of components (3) to (5) are added to A, and the mixture is mixed and dispersed uniformly using a roll mill. C: A portion of the components (3) to (5), a portion of the components (1) and (2), and the components (17) to (19) are uniformly mixed and dispersed in a roll mill. D: To B, add C, the remaining components (1) and (2), the remaining components (3) to (5), component (9), and components (22) to (24) and mix uniformly, then add components (20) and (21) which have been heated and dissolved. E: Add components (25) to (28) to D and emulsify using a disperser mixer at 2000 rpm at room temperature for 5 minutes. F: E was filled into a tube container to obtain a water-in-oil BB cream.

[0075] The water-in-oil BB cream of Example 27 obtained in the above manner had excellent drying speed, uniformity, cosmetic durability, and adhesion.

[0076] Example 28: Water-in-oil two-layer shaking foundation A water-in-oil two-layer shaking foundation was prepared according to the composition and manufacturing method described below. (Component) (%) (1) Isododecane *3 6 (2) Hydrogenated polyisobutene 6 (3) Lauryl PEG-9 Polydimethylsiloxyethyl Dimethicone 0.6 (4) PEG-9 Polydimethylsiloxyethyl Dimethicone 0.4 (5) Polyglyceryl-6 polyricinoleate (HLB 3.3) 2 (6) Olive fruit oil 0.1 (7) Rosa canina fruit oil 0.1 (8) Jojoba oil 0.1 (9) Sesame seed oil 0.1 (10) Rosemary Leaf Extract 0.1 (11) Lavender oil 0.1 (12) Propylene glycol dicaprylate 3 (13) (Acrylates / Dimethicone) Copolymer *7 (Solids content 40% in isododecane) 2 (14) Titanium dioxide treated with 3% disodium N-stearoyl-L-glutamate (average particle size 270 nm) 9 (15) Fine particle titanium dioxide (average particle diameter 35 nm) treated with 3% aluminum hydroxide, 5.5% hydrated silica, and 3% zinc laurate 7 (16) Pigment-grade titanium dioxide (average particle size 250 nm) treated with 3% zinc laurate 1 (17) Black iron oxide 0.2 (18) Red iron oxide 0.3 (19) Yellow iron oxide 0.6 (20) Shea butter 0.5 (21) Polyglyceryl-3 distearate 0.6 (22) Silicone polyurethane gel composition of Production Example 4 of component (A) (30% 6CS solvent) 2 (23) Benzyl dimethylstearyl ammonium hectorite 0.6 (24) Dimethyl distearyl ammonium hectorite 1.5 (25) Ethylhexyl methoxycinnamate 6 (26) Spherical Silica 5 (27) Titanium mica (average particle size 15 μm) 5 (28) Talc*11 5 (29) Remaining purified water (30) Ethanol 5 (31) Tripropylene glycol 10 (32) 1,3-Butylene glycol 10 (17), (18), and (19) may be metal oxides treated with zinc stearate, sodium dilauroyl glutamate lysine, methylpolysiloxane, hydrogenpolysiloxane triethoxycaprylylsilane, or aminopropyltriethoxysilane.

[0077] (Manufacturing method) A: Heat ingredients (6)-(12), (20), (21), and (22) to 80°C and mix and dissolve uniformly. B: Components (14) to (19) and a portion of components (3) to (5) are added to A, and the mixture is mixed and dispersed uniformly using a roll mill. C: A portion of components (1) and (2), a portion of components (3) to (5), and components (23) to (24) are uniformly mixed and dispersed. D: To B, add C, the remaining components (1) and (2), the remaining components (3) through (5), component (13), and components (25) through (28), and mix and disperse uniformly. E: Add components (29) to (32) to D and emulsify using a disperser mixer at 2000 rpm at room temperature for 5 minutes. F: E was filled into a bottle container to obtain a water-in-oil type two-layer shaking foundation.

[0078] The water-in-oil two-layer shaking foundation of Example 28 obtained as described above was excellent in the drying speed of the coating film, the uniformity of the coating film, the cosmetic durability and the adhesion.

[0079] Example 29: Water-in-oil type sunscreen cosmetic A water-in-oil sunscreen was prepared according to the composition and manufacturing method shown below. (Component) (%) (1) Isododecane *3 6 (2) Hydrogenated polyisobutene 6 (3) Alkyl benzoate (C12-15) 5 (4) Lauryl PEG-9 Polydimethylsiloxyethyl Dimethicone 1.2 (5) PEG-9 Polydimethylsiloxyethyl Dimethicone 0.8 (6) Polyglyceryl-3 distearate 1 (7) Olive fruit oil 0.1 (8) Rosa canina fruit oil 0.1 (9) Jojoba oil 0.1 (10) Sesame seed oil 0.1 (11) Rosemary Leaf Extract 0.1 (12) Propylene glycol dicaprylate 3 (13) (Acrylates / Dimethicone) Copolymer *7 (Solids content 40% isododecane solution) 2 (14) (Vinyl dimethicone / methicone silsesquioxane) crosspolymer *25 2 (15) Fine particle titanium dioxide (average particle diameter 35 nm) treated with 3% aluminum hydroxide, 5.5% hydrated silica, and 3% zinc laurate 10 (16) Shea butter 0.5 (17) Silicone polyurethane gel composition of Production Example 4 of component (A) (30% 6CS solvent) 2 (18) Ethylhexyl methoxycinnamate 6 (19) Cetyl dimethicone 1 (20) Spherical Silica 5 (21) Titanium mica (average particle size 15 μm) 5 (22) Talc*11 5 (23) Remaining purified water (24) Ethanol 5 (25) Tripropylene glycol 10 (26) 1,3-Butylene glycol 10 *25: KSP-100 / average particle size: 5μm / non-porous (manufactured by Shin-Etsu Chemical Co., Ltd.) (15) may be a metal oxide treated with zinc stearate, sodium dilauroyl glutamate lysine, methylpolysiloxane, hydrogenpolysiloxane triethoxycaprylylsilane, or aminopropyltriethoxysilane.

[0080] (Manufacturing method) A: Heat ingredients (7)-(12), (16), and (17) to 80°C and mix and dissolve uniformly. B: Component (15) and a portion of components (4) to (6) are added to A and mixed and dispersed uniformly using a media disperser. C: Add components (1) through (3), the remaining components (4) through (6), components (13), (14), and components (18) through (22) to B and mix and disperse uniformly. D: Add ingredients (23) to (26) to C and emulsify using a disperser mixer at 2000 rpm at room temperature for 5 minutes. E:D was filled into a bottle container to obtain a water-in-oil sunscreen.

[0081] The water-in-oil sunscreen of Example 29 obtained as described above had excellent drying speed, uniformity, cosmetic durability and adhesion.

[0082] Example 30: Water-in-oil mascara cosmetic A water-in-oil mascara cosmetic was prepared using the composition and production method described below. (composition) (%) (1) Isododecane *3 12 (2) Hydrogenated polyisobutene 20 (3) Lauryl PEG-9 Polydimethylsiloxyethyl Dimethicone 0.1 (4) PEG-9 Polydimethylsiloxyethyl Dimethicone 0.2 (5) Polyglyceryl-3 distearate 0.2 (6) Almond oil 0.1 (7) Peach kernel oil 0.1 (8) Safflower oil 0.1 (9) Sesame seed oil 0.1 (10) Camellia seed oil 0.1 (11) Tocopherol 0.0001 (12) Decamethyltetrasiloxane 3 (13) Trimethylsiloxysilicate *5 8 (14) (Ethylene / propylene) copolymer 0.5 (15) Silicone polyurethane gel composition of Production Example 3 of component (A) (30% 2CS solvent) 4 (16) Black iron oxide 10.0 (17) Red iron oxide 0.2 (18) Yellow iron oxide 0.6 (19) Shea butter 0.5 (20) Microcrystalline wax 3 (21) Dextrin palmitate*1 1 (22) Dextrin isostearate*15 0.5 (23) Candelilla Wax *13 0.5 (24) Carnauba wax *2 4 (25) Dimethyl distearyl ammonium hectorite *17 1.5 (26) Benzyl dimethylstearyl ammonium hectorite 0.6 (27) Propylene carbonate 0.3 (28) Polyglyceryl-6 polyricinoleate (HLB 3.3) 2 (29) Spherical Silica 5 (30) Nylon-12 *26 5 (31) Talc*11 5 (32) Remaining purified water (33) Ethanol 1 (34) Tripropylene glycol 0.2 (35) 1.3-Butylene glycol 0.5 (36) Methylparaben 0.1 *26: Orgasol 2002D / average particle size 20μm / porous (manufactured by Atofina Japan) (15), (16), and (17) may be metal oxides treated with zinc stearate, sodium dilauroyl glutamate lysine, methylpolysiloxane, hydrogenpolysiloxane triethoxycaprylylsilane, or aminopropyltriethoxysilane.

[0083] (Manufacturing method) A: Heat components (14), (15), (19)-(24), and a portion of (2)-(5) to 90°C and mix and dissolve uniformly. B: A portion of components (3)-(5), components (4)-(12), and components (16)-(18) are added to A, and the mixture is uniformly mixed and dispersed using a hot roll mill. C: Components (25) to (28) and a portion of component (2) are uniformly mixed and dispersed in a roll mill. D: Add C, the remaining components (1), (2) through (5), component (13), and components (29) through (31) to B and mix and disperse uniformly. E: Add components (32) to (36) to D and emulsify using a disperser mixer at 2000 rpm at room temperature for 5 minutes. F: E was filled into a container equipped with an applicator to obtain a water-in-oil mascara cosmetic.

[0084] The water-in-oil mascara cosmetic of Example 30 obtained as described above was excellent in the drying speed of the coating film, the uniformity of the coating film, cosmetic durability and adhesion.

[0085] Example 31: Oil-in-water emulsion foundation (Component) (%) (1) Titanium dioxide treated with 2% triethoxycaprylylsilane (average particle size 0.27 μm) 2 (2) Dimethylpolysiloxane 7% treated silica-coated titanium dioxide (average particle size 35 nm) 5 (3) Glyceryl triethylhexanoate 2.5 (4) Dimethylpolysiloxane (25°C, kinematic viscosity 20CS) 2.5 (5) Squalane 2 (6) Diethylamino hydroxybenzoyl hexyl benzoate 1.5 (7) 2-Ethylhexyl p-methoxycinnamate 5 (8) Behenyl alcohol 1.0 (9) Sucrose fatty acid ester 1.0 (10) Stearic acid 1.5 (11) Glyceryl monostearate 0.2 (12) Polyoxyethylene sorbitan oleate (20E.O.) 0.5 (13) Silicone polyurethane gel composition of Production Example 4 of component (A) (30% 6CS solution) 2 (14) (Acrylates / Dimethicone) Copolymer*7 (Solids content 40% isododecane solution) 0.6 (15) (Sodium acrylate / sodium acryloyldimethyltaurate) copolymer*27 1 (16) Triethanolamine 1 (17) Lecithin*100.5% treated titanium dioxide (average particle size 250 nm) 5 (18) Yellow iron oxide 1.2 (19) Red iron oxide 0.8 (20) Black iron oxide 0.4 (21) Talc*11 2 (22) Methyl parahydroxybenzoate 0.1 (23) 1,3-Butylene glycol 3 (24) Dipropylene glycol (DPG) 10 (25) Remaining purified water *27:SIMLGEL EG (manufactured by SEPPIC)

[0086] (Manufacturing method) A. Disperse ingredients (1) to (4) using a roller mill. B. Heat ingredients (5) to (14) to 70°C, add A and mix uniformly. C. Disperse components (17) to (23) in a roller mill, and then add components (15), (16), (24), and (25) and mix uniformly. Gradually add B to EC and emulsify at 70°C, cool to 35°C, degas, and fill into containers to produce the product.

[0087] The oil-in-water emulsion foundation thus obtained was excellent in drying speed, uniformity, cosmetic durability and adhesion.

[0088] Example 32: Oil-in-water emulsion mascara (Component) (%) (1) Isododecane *3 3 (2) Trimethylsiloxysilicate *5 1.5 (3) Silicone polyurethane gel composition of Production Example 4 (30% 6CS solvent) 3 (4) Candelilla wax *13 3 (5) Carnauba wax *2 2 (6) Beeswax 3 (7) Stearic acid 1.5 (8) Myristic acid 0.5 (9) Hydrogenated glyceryl abietic acid *21 1 (10) Sorbitan sesquioleate 0.3 (11) Polyoxyethylene sorbitan monooleate (20E.O.) 1 (12) Black iron oxide 4 (13) Carmine 1.5 (14) Remaining purified water (15) Polyvinyl alcohol 1 (16) Ethanol 1 (17) 1,3-Butylene glycol 1 (18) EDTA-2Na 0.1 (19) Sodium dehydroacetate 0.1 (20) Methyl parahydroxybenzoate 0.2 (21) Phenoxyethanol 0.3 (22) Sodium hyaluronate 0.1 (23) Tocopherol 0.1 (24) (Acrylates / Ethylhexyl acrylate) Copolymer* 29 10 (25) (Acrylates / VA) copolymer *30 3 (26) Polyvinyl acetate *31 2 *29: Daitosol 5000SJ (50% solids by mass, solvent: water) (manufactured by Daido Chemical Industry Co., Ltd.) *30: Vinisole 2140L (43% solids by mass, solvent: water) (manufactured by Daido Chemical Industry Co., Ltd.) *31: Vinybran GV-5651 (40% solids by mass, solvent: water) (manufactured by Nissin Chemical Industry Co., Ltd.)

[0089] (Manufacturing method) A. Heat ingredients (1) to (11) to 100°C and mix uniformly. Add components (12) and (13) to BA and disperse uniformly at 80°C. C. Uniformly disperse ingredients (14) to (26) at 80°C. Add C to DB and emulsify at 80℃. The CD is cooled to room temperature and filled into a container with an applicator (nylon brush) to make the product.

[0090] The oil-in-water emulsion mascara of the present invention was excellent in drying speed, uniformity, cosmetic durability and adhesion.

[0091] Example 33: Oily solid lipstick (Component) (%) (1) Isododecane *3 4 (2) Trimethylsiloxysilicate *5 1.5 (3) Silicone polyurethane gel composition of Production Example 3 (30% 2CS solvent) (4) Candelilla wax *13 2 (5) (Ethylene / propylene) copolymer 4 (6) Polyethylene wax 4 (7) Tridecyl trimellitate *32 5 (8) Triethylhexanoin *33 10 (9) Diisostearyl malate *34 5 (10) Diglyceryl triisostearate *35 balance (11) Tridecyl isononanoate *36 3 (12) Hydrogenated polyisobutene 2 (13) Dimer dilinoleic acid (phytosteryl / isostearyl / cetyl / stearyl / behenyl) *37 3 (14) Vaseline 3 (15) Diphenyl dimethicone *38 5 (16) Silylated Silica 1 (17) (Vinyl dimethicone / methicone silsesquioxane) crosspolymer *39 3 (18) Red No. 202 0.5 (19) Yellow No. 4 0.6 (20) Titanium dioxide 1.1 (21) Black iron oxide 0.15 *32:LIPONATE TDTM (manufactured by LIPO CHEMICALS) *33: MYRITOL GTEH (manufactured by BASF) *34: Himalate DIS (manufactured by Koyu Alcohol Co., Ltd.) *35: Cosmol 43V (manufactured by Nisshin Oillio Co., Ltd.) *36: Salakos 913 (manufactured by Nisshin Oillio Co., Ltd.) *37: PLANDOOL-S (manufactured by Nippon Fine Chemicals) *38: KF-54 (manufactured by Shin-Etsu Chemical Co., Ltd.) *39:KSP-102 (Shin-Etsu Chemical Co., Ltd.)

[0092] (Manufacturing method) A. Heat ingredients (1) to (15) to 100°C and mix uniformly. 0.08 Components (16) to (21) are added to BA, and mixed and dispersed uniformly while cooling using a roll mill. C: B is melted at 110°C, poured into a mold container, and then cooled. D: Load C into the container.

[0093] The oily solid lipstick of the present invention was excellent in drying speed of the coating film, uniformity of the coating film, cosmetic durability and adhesion.

Claims

1. The following components (A) to (C): (A) Formula (1) below OCN-R 1 -NCO (1) (In the formula, R 1 represents an alkylene group having 2 to 9 carbon atoms. A structural unit based on an isocyanate compound represented by the formula: The following formula (2) 【Chemistry 1】 (wherein n represents an integer of 1 to 100). A structural unit based on dimethiconol represented by the formula: The following formula (3) HO-R 2 -OH (3) (In the formula, R 2 represents a linear or branched alkylene group having 2 to 9 carbon atoms which may have an ether bond. and a silicone polyurethane having a structural unit based on an alkylene glycol represented by the formula: (B) Oil-soluble film-forming agent (C) Volatile oil A cosmetic preparation comprising:

2. 2. The cosmetic according to claim 1, wherein the component (B) contains (B-1) a silicone-based resin.

3. 3. The cosmetic preparation according to claim 2, wherein the mass ratio (B-1) / (B) of the component (B-1) to the component (B) is 0.3 to 1.

0.

4. 3. The cosmetic preparation according to claim 1, wherein the mass ratio (A) / (B) of the component (A) to the component (B) is 0.01 to 2.

5.

5. 3. The cosmetic preparation according to claim 1, wherein the content of the component (A) is 0.1 to 10% by mass.

6. 3. The cosmetic preparation according to claim 1, wherein the content of the component (B) is 1 to 25% by mass.

7. 3. The cosmetic preparation according to claim 1, further comprising a component (D) a wax.

8. 3. The cosmetic preparation according to claim 1, further comprising a dextrin fatty acid ester as component (E).

9. The cosmetic according to claim 1 or 2, which is selected from the group consisting of oil-based cosmetics and water-in-oil cosmetics.

10. 3. The cosmetic according to claim 1, which is an eye makeup cosmetic.

11. 3. The cosmetic according to claim 1, which is a hair cosmetic.

Citation Information

Patent Citations

  • Mascara product having polyurethane

    JP2000178137A

  • Eyelashes cosmetics

    JP2017132732A

Cited By

  • Water-in-oil emulsion cosmetic

    WO2026088587A1