WO2013065486A1 - Cosmetic composition - Google Patents

Cosmetic composition Download PDF

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Publication number
WO2013065486A1
WO2013065486A1 PCT/JP2012/076832 JP2012076832W WO2013065486A1 WO 2013065486 A1 WO2013065486 A1 WO 2013065486A1 JP 2012076832 W JP2012076832 W JP 2012076832W WO 2013065486 A1 WO2013065486 A1 WO 2013065486A1
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WIPO (PCT)
Prior art keywords
mono
cosmetic composition
weight
polyglycerin
silicone oil
Prior art date
Application number
PCT/JP2012/076832
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French (fr)
Japanese (ja)
Inventor
前原徹也
坂西裕一
Original Assignee
株式会社ダイセル
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Priority claimed from JP2011240901A external-priority patent/JP2013095713A/en
Priority claimed from JP2011240902A external-priority patent/JP5886599B2/en
Application filed by 株式会社ダイセル filed Critical 株式会社ダイセル
Publication of WO2013065486A1 publication Critical patent/WO2013065486A1/en

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    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/33Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
    • A61K8/37Esters of carboxylic acids
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/33Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
    • A61K8/39Derivatives containing from 2 to 10 oxyalkylene groups
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/72Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
    • A61K8/84Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions otherwise than those involving only carbon-carbon unsaturated bonds
    • A61K8/89Polysiloxanes
    • A61K8/891Polysiloxanes saturated, e.g. dimethicone, phenyl trimethicone, C24-C28 methicone or stearyl dimethicone
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q1/00Make-up preparations; Body powders; Preparations for removing make-up
    • A61Q1/14Preparations for removing make-up

Definitions

  • the present invention relates to a lotion type cosmetic composition.
  • lotion-type cosmetic compositions for example, cleansing lotions and the like
  • water usually about 70 to 90% by weight of the total amount of the cosmetic composition
  • oily component usually about 70 to 90% by weight of the total amount of the cosmetic composition
  • surfactant a blend of ingredients was provided.
  • cleansing lotions are required to have excellent detergency that can be used for washing highly hydrophobic cosmetics such as waterproof mascara.
  • cleansing lotions that do not contain oily ingredients that cause stickiness have been provided.
  • a cleansing lotion that does not contain an oil component has no stickiness and a refreshing feeling of use, but the cleaning power is reduced.
  • the amount of the surfactant is increased in order to improve the detergency, not only the stickiness peculiar to the surfactant is generated, but also the skin irritation becomes strong and may cause inflammation. For this reason, it is difficult to combine detergency, usability, and safety.
  • silicone oil is easily adapted to cosmetics when applied to the skin surface, and has a characteristic characteristic of oily components that allows the cosmetics to quickly rise from the skin surface, but does not feel sticky like other oily components. Therefore, development of a cosmetic composition having a non-stickiness and an excellent detergency, in which silicone oil is blended as an oil component has been performed.
  • silicone oil is extremely difficult to solubilize in water and mixes with water, it has an opaque appearance and impairs aesthetics.Therefore, it has sufficient detergency for highly hydrophobic cosmetics such as waterproof mascara. It has been difficult to prepare a lotion-type cosmetic composition containing an amount of silicone oil that is sufficient to exhibit the above.
  • Patent Document 1 As a method for solubilizing silicone oil without increasing the amount of surfactant, a method using an alcohol such as ethanol as a solubilizing aid together with a surfactant is known (Patent Document 1).
  • alcohols with high solubilizing power for example, ethanol
  • an object of the present invention is to provide a lotion-type transparent cosmetic composition having no stickiness, excellent usability, and excellent detergency.
  • a low-irritant lotion-type cosmetic composition that can significantly improve the solubility of silicone oil in water, contains silicone oil, water, and the surfactant, and contains 80% by weight or more of the water.
  • the cosmetic composition contains a silicone oil that does not have a sticky feeling peculiar to an oily component as an oily component, so that the cosmetic composition has a high hydrophobicity such as a waterproof mascara.
  • Silicone with excellent detergency, no stickiness and excellent usability Yl is contained within a stable O / W type micelle by surfactant, it is highly dispersed to form a microemulsion in water, since the dispersion state is maintained, was found to have a transparent appearance.
  • the present invention has been completed based on these findings.
  • the present invention is a cosmetic composition containing mono- or polyglycerin alkyl or alkenyl ether (a1) and / or mono- or polyglycerin fatty acid ester (a2), silicone oil (b), and water (c).
  • the cosmetic composition is characterized in that the water content is 80% by weight or more of the total amount of the cosmetic composition.
  • R 1 represents a linear or branched alkyl group or alkenyl group having 8 to 22 carbon atoms which may have a hydroxyl group.
  • N 1 represents the average degree of polymerization of glycerin, 1 to 10.
  • the mono- or polyglycerin monoalkyl or alkenyl ether represented by the formula (1) is preferred, and the HLB value is preferably 8.0 to 12.0.
  • R 2 represents a linear or branched aliphatic hydrocarbon group having 8 to 22 carbon atoms which may have a hydroxyl group.
  • N 2 represents the average degree of polymerization of glycerin, 1 to 10)
  • a compound having an HLB value of 9.0 to 15.0 is preferred.
  • the content of the mono- or polyglycerin alkyl or alkenyl ether (a1), silicone oil (b), and water (c) relative to the total amount of the cosmetic composition is: The following range is preferable.
  • the content of the mono- or polyglycerin fatty acid ester (a2), silicone oil (b), and water (c) relative to the total amount of the cosmetic composition The following range is preferable.
  • mono or polyglycerol alkyl or alkenyl ether (a1) and mono or polyglycerol fatty acid ester (a2) mono or polyglycerol alkyl or alkenyl ether (a1), mono or polyglycerol fatty acid ester (a2), silicone oil, And as content with respect to the cosmetics composition whole quantity of water, it is preferable that it is the following range.
  • the cosmetic composition according to the present invention contains, as an oil component, a silicone oil that does not have a sticky feeling peculiar to an oil component, so that it is excellent for highly hydrophobic cosmetics such as a waterproof mascara. While having power, it has an excellent feeling of use without stickiness. Then, the silicone oil forms a stable micelle by the surface active action of hypoallergenic mono- or polyglyceryl alkyl or alkenyl ether and / or mono- or polyglycerin fatty acid ester, and is highly dispersed in water to form a microemulsion. Therefore, it has a transparent appearance and is excellent in safety. That is, the cosmetic composition according to the present invention can be suitably used as a cleansing lotion having an excellent appearance and an excellent detergency, safety and usability.
  • the cosmetic composition of the present invention uses a mono- or polyglycerin alkyl or alkenyl ether (a1) and / or a mono- or polyglycerin fatty acid ester (a2) that is low in irritation and excellent in safety as a surfactant.
  • Examples of the mono- or polyglycerin alkyl or alkenyl ether (a1) include monoglycerin monoalkyl or alkenyl ether, monoglycerin dialkyl or alkenyl ether, polyglycerin monoalkyl or alkenyl ether, and polyglycerin dialkyl or alkenyl ether.
  • mono- or polyglycerin monoalkyl or alkenyl ether represented by the following formula (1) is preferable in that it has excellent power (solubilization power) for solubilizing highly hydrophobic silicone oil in water.
  • R 1 represents a linear or branched alkyl group or alkenyl group having 8 to 22 carbon atoms which may have a hydroxyl group.
  • n 1 represents an average degree of polymerization of glycerin and is 1 to 10.
  • C 3 H 6 O 2 in parentheses in the formula (1) has both structures represented by the following formulas (3) and (4).
  • R 1 represents a linear or branched alkyl group or alkenyl group having 8 to 22 carbon atoms which may have a hydroxyl group.
  • Examples of the linear alkyl group having 8 to 22 carbon atoms include n-octyl, n-nonyl, n-decyl, n-undecyl, n-lauryl, n-tridecyl, n-tetradecyl, n-pentadecyl, n- Examples include palmityl, n-heptadecyl, n-stearyl, n-nonadecyl, n-eicosyl, n-heneicosyl, n-docosyl group and the like.
  • linear alkenyl group having 8 to 22 carbon atoms examples include n-octenyl, n-nonenyl, n-decenyl, n-undecenyl, n-dodecenyl, n-tridecenyl, n-tetradecenyl, n-pentadecenyl, n- Examples include hexadecenyl, n-heptadecenyl, n-eylidyl, n-oleyl, n-nonadecenyl, n-gadoleyl, n-eicosenyl, n-heneicosenyl, n-docosenyl and the like.
  • linear alkyl group or alkenyl group having 8 to 22 carbon atoms and having a hydroxyl group one or more hydrogen atoms of the linear alkyl group or alkenyl group having 8 to 22 carbon atoms are substituted with a hydroxyl group.
  • the group can be mentioned.
  • Examples of the branched alkyl group having 8 to 22 carbon atoms include isooctyl, s-octyl, t-octyl, isononyl, s-nonyl, t-nonyl, isodecyl, s-decyl, t-decyl, isoundecyl, s- Undecyl, t-undecyl, isolauryl, s-lauryl, t-lauryl, isotridecyl, s-tridecyl, t-tridecyl, isotetradecyl, s-tetradecyl, t-tetradecyl, isopentadecyl, s-pentadecyl, t-pentadecyl, Isopalmityl, 2-hexyldecyl, s-palmityl, t-palmity
  • Examples of the branched alkenyl group having 8 to 22 carbon atoms include isooctenyl, s-octenyl, t-octenyl, isononenyl, s-nonenyl, t-nonenyl, isodecenyl, s-decenyl, t-decenyl, isoundecenyl, s- Undecenyl, t-undecenyl, isododecenyl, s-dodecenyl, t-dodecenyl, isotridecenyl, s-tridecenyl, t-tridecenyl, isotetradecenyl, s-tetradecenyl, t-tetradecenyl, isopentadecenyl, s-pentadecenyl, t-pentadecenyl, is
  • branched alkyl group or alkenyl group having 8 to 22 carbon atoms having a hydroxyl group one or more hydrogen atoms of the branched alkyl group or alkenyl group having 8 to 22 carbon atoms is substituted with a hydroxyl group.
  • the group can be mentioned.
  • R 1 is a straight chain having 8 to 22 carbon atoms because it has high water solubility and excellent solubilizing power of silicone oil.
  • a linear or branched alkyl group is preferable, and a linear alkyl group having 8 to 22 carbon atoms (particularly 12 to 14 carbon atoms) such as an n-lauryl group or an n-myristyl group is particularly preferable.
  • n 1 represents an average degree of polymerization of glycerin, and is, for example, 1 to 10, preferably 1 to 5, particularly preferably 1 to 3.
  • the value of n 1 is less than 1, the hydrophobicity increases and the water solubilizing power tends to decrease.
  • n 1 exceeds 10, hydrophilicity tends to increase and solubilizing power to silicone oil tends to decrease.
  • the production method of the mono- or polyglycerin monoalkyl or alkenyl ether (a1) represented by the above formula (1) is not particularly limited.
  • a basic catalyst A method in which glycidol is added and reacted so that the abundance ratio (molar ratio) of the alcohol and glycidol is a specific value; a method in which an ⁇ -olefin epoxide is reacted with mono- or polyglycerin; in the presence of an acid catalyst or an alkali catalyst And a method of opening a ring of alkyl glycidyl ether using mono- or polyglycerin.
  • the HLB value of the mono- or polyglycerin alkyl or alkenyl ether (a1) in the present invention is, for example, 8.0 to 12.0, preferably 9.0 to 11.0, particularly preferably 9.5 or more, 11.0. Is less than.
  • the HLB value is below the above range, the hydrophobicity becomes too high, and mono- or polyglycerin alkyl or alkenyl ether dissolves only in silicone oil, and it tends to be difficult to dissolve in water, making it difficult to form a microemulsion. Tend to be.
  • the HLB value exceeds the above range, the hydrophilicity becomes too high, mono- or polyglycerin alkyl or alkenyl ether is dissolved only in water, and it tends to be difficult to dissolve in silicone oil. It tends to be difficult.
  • the HLB value can be decreased by increasing the number of carbon atoms of the alkyl group or alkenyl group, and can be increased by increasing the degree of polymerization of polyglycerol. Therefore, the HLB value can be adjusted by controlling the above molecular structure.
  • Preferred examples of the mono- or polyglycerin alkyl or alkenyl ether (a1) in the present invention include monoglycerin monolauryl ether (HLB value: 8.5), diglycerin monolauryl ether (HLB value: 10.6), triglycerin. And monomyristyl ether (HLB value: 11.0). These can be used alone or in combination of two or more.
  • the cosmetic composition of the present invention uses a mono- or polyglycerin alkyl or alkenyl ether (a1) and / or a mono- or polyglycerin fatty acid ester (a2) that is low in irritation and excellent in safety as a surfactant.
  • the mono- or polyglycerin fatty acid ester (a2) is represented by the following formula (2).
  • R 2 represents a linear or branched aliphatic hydrocarbon group having 8 to 22 carbon atoms which may have a hydroxyl group.
  • n 2 represents the average degree of polymerization of glycerin and is 1 to 10.
  • C 3 H 6 O 2 in parentheses in the formula (2) has both structures represented by the following formulas (5) and (6).
  • R 2 represents a linear or branched aliphatic hydrocarbon group having 8 to 22 carbon atoms which may have a hydroxyl group.
  • Examples of the linear aliphatic hydrocarbon group having 8 to 22 carbon atoms include n-octyl, n-nonyl, n-decyl, n-undecyl, n-lauryl, n-tridecyl, n-tetradecyl, and n-pentadecyl.
  • C 8-22 straight chain alkyl groups such as n-palmityl, n-heptadecyl, n-stearyl, n-nonadecyl, n-eicosyl, n-heneicosyl, n-docosyl; n-octenyl, n-nonenyl, n- Decenyl, n-undecenyl, n-dodecenyl, n-tridecenyl, n-tetradecenyl, n-pentadecenyl, n-hexadecenyl, n-heptadecenyl, n-elaidyl, n-oleyl, n-nonadecenyl, n-gadoleyl, n-eicosenyl, Examples thereof include C 8-22 straight chain alkenyl groups such as n-heneicosenyl and n-
  • linear aliphatic hydrocarbon group having 8 to 22 carbon atoms and having a hydroxyl group one or more hydrogen atoms of the above linear aliphatic hydrocarbon group having 8 to 22 carbon atoms are substituted with a hydroxyl group.
  • the group can be mentioned.
  • Examples of the branched aliphatic hydrocarbon group having 8 to 22 carbon atoms include isooctyl, s-octyl, t-octyl, isononyl, s-nonyl, t-nonyl, isodecyl, s-decyl, t-decyl, and isoundecyl.
  • branched aliphatic hydrocarbon group having 8 to 22 carbon atoms and having a hydroxyl group one or more hydrogen atoms of the branched aliphatic hydrocarbon group having 8 to 22 carbon atoms are substituted with a hydroxyl group.
  • the group can be mentioned.
  • R 2 in the formula (2) is a linear or branched group having 8 to 22 carbon atoms, particularly in terms of the excellent solubilizing power of silicone oil.
  • a chain alkyl group is preferable, and a linear alkyl group having 8 to 22 carbon atoms (particularly 12 to 14 carbon atoms) such as an n-lauryl group and an n-myristyl group is particularly preferable.
  • n 2 represents the average degree of polymerization of glycerin, and is, for example, 1 to 10, preferably 1 to 5, and particularly preferably 1 to 3.
  • the value of n 2 is less than 1, the hydrophobicity increases and the water solubilizing power tends to decrease.
  • n 2 exceeds 10, hydrophilicity tends to increase and solubilizing power to silicone oil tends to decrease.
  • the HLB value of the mono- or polyglycerin fatty acid ester (a2) in the present invention is, for example, 9.0 to 15.0, preferably 9.0 to 13.0, and particularly preferably 9.0 to 12.0.
  • the HLB value is less than the above range, the hydrophobicity becomes too high, and the mono- or polyglycerin fatty acid ester tends to dissolve only in the silicone oil, making it difficult to dissolve in water.
  • the HLB value exceeds the above range, the hydrophilicity becomes too high, and the mono- or polyglycerin fatty acid ester tends to be soluble only in water and difficult to dissolve in silicone oil.
  • the HLB value can be increased by increasing the number of carbon atoms of the fatty acid residue, and can be increased by increasing the polymerization degree of the polyglycerol. Therefore, the HLB value can be adjusted by controlling the above molecular structure.
  • Preferred examples of the mono- or polyglycerin fatty acid ester (a2) in the present invention include diglycerin monolaurate and diglycerin monomyristate. These can be used alone or in combination of two or more.
  • the trade name “Poem DL-100” diglycerin monolaurate, HLB: 9.4, manufactured by Riken Vitamin Co., Ltd.
  • the trade name “Poem DM-100” diglycerin monomyristate
  • Commercial products such as rate, HLB: 10.1, manufactured by Riken Vitamin Co., Ltd. can be preferably used.
  • the silicone oil (b) of the present invention may be at least a polysiloxane having a main chain composed of a siloxane bond, and may have a substituent at the end of the main chain and / or the side chain.
  • the main chain may form a ring.
  • Silicone oil (b) includes straight silicone oil and modified silicone oil.
  • the straight silicone oil is a polysiloxane whose main chain is composed of a siloxane bond, and when it has a substituent, the substituent is a methyl group and / or a phenyl group, and has no substituent other than a methyl group and a phenyl group. .
  • the bonding position of the substituent in the straight silicone oil is not particularly limited, and both ends of the main chain (both ends type: represented by the following formula (7)) or one end (one end type: represented by the following formula (8) May be present on the side chain (side chain type: represented by the following formula (9)), and has a substituent on the side chain and both ends.
  • the side chain and both terminal types: represented by the following formula (10) may further have a substituent on the side chain and one terminal (side chain and one terminal type: the following formula (11) )). All side chains and terminals may be substituted with methyl groups (represented by the following formula (12)).
  • the compounds represented by the following formulas (9) to (11) may be any of random copolymers, alternating copolymers, block copolymers and the like.
  • X 1 , X 2 and X 3 in the above formula are a hydrogen atom or a phenyl group, and m and n are integers of 1 or more. X 1 , X 2 and X 3 may be the same or different. m and n may also be the same or different.
  • the straight silicone oil include all side chains, dimethyl silicone having a terminal methyl group, and cyclic dimethyl silicone in which the dimethyl silicone forms a ring, methyl phenyl having a phenyl group in a part of the side chain.
  • examples thereof include silicone and methyl hydrogen silicone in which a part of the side chain is hydrogen.
  • cyclopentasiloxane, diphenylsiloxyphenyl trimethicone and the like are preferable because they have excellent detergency and less stickiness.
  • the modified silicone oil is a polysiloxane whose main chain is composed of a siloxane bond, and has a substituent other than a methyl group and a phenyl group.
  • the bonding position of the substituent in the modified silicone oil is not particularly limited, and both ends of the main chain (both ends type: represented by the following formula (13)) or one end (one end type: the following formula (14) May be present in the side chain (side chain type: represented by the following formula (15)), and has a substituent on the side chain and at both ends.
  • a side chain and both terminal types: represented by the following formula (16)) and may further have a substituent on the side chain and one terminal (side chain and one terminal type: the following formula ( 17)).
  • the compounds represented by the following formulas (15) to (17) may be any of random copolymers, alternating copolymers, block copolymers and the like.
  • X 4 , X 5 and X 6 are substituents (other than methyl group and phenyl group), and m ′ and n ′ are integers of 1 or more.
  • X 4 , X 5 and X 6 may be the same or different.
  • m ′ and n ′ may also be the same or different.
  • Examples of the substituent other than the methyl group and the phenyl group in X 4 , X 5 and X 6 in the above formula include, for example, an alkyl group having 2 or more carbon atoms, an aralkyl group, an epoxy group, a fluorine atom, an amino group, a carboxyl group, Examples include aliphatic hydroxyl groups (alcoholic hydroxyl groups), aromatic hydroxyl groups other than phenyl groups (phenolic hydroxyl groups), (meth) acryloyl group-containing substituents, substituents containing polyether chains, and the like.
  • modified silicone oil in the present invention among them, a modified silicone oil having an alkyl group having 2 or more carbon atoms as a substituent is preferable in that it can further improve the detergency.
  • Modified silicone oils having 18 to 18 linear or branched alkyl groups (for example, lauryl group, cetyl group, etc.) in the side chain are preferred.
  • commercial names such as “SS-3408” (caprylylmethicone, manufactured by Toray Dow Corning) and “2502 Cosmetic Fluid” (cetyl dimethicone, manufactured by Toray Dow Corning) are commercially available. The product can be suitably used.
  • silicone oil in the present invention for example, trade name “KF-995” (cyclopentasiloxane, manufactured by Shin-Etsu Silicone Co., Ltd.), trade name “KF-56A” (diphenylsiloxyphenyl trimethicone, manufactured by Shin-Etsu Silicone Co., Ltd.) ), Etc., trade names such as “SS-3408” (caprylyl methicone, manufactured by Toray Dow Corning Co., Ltd.), “2502 Cosmetic Fluid” (cetyl dimethicone, manufactured by Toray Dow Corning Co., Ltd.), etc.
  • a side chain type alkyl-modified silicone oil or the like can be preferably used. These can be used alone or in combination of two or more.
  • the cosmetic composition of the present invention comprises a mono- or polyglycerin alkyl or alkenyl ether (a1) and / or a mono- or polyglycerin fatty acid ester (a2), a silicone oil (b), and water (c).
  • the water content is 80.0% by weight or more of the total amount of the cosmetic composition.
  • the mono- or polyglycerin fatty acid ester (a2) when the mono- or polyglycerin fatty acid ester (a2) is not used and the mono- or polyglycerin alkyl or alkenyl ether (a1) is used, It is 80.0% by weight or more of the total amount of the composition, preferably about 86.0 to 93.0% by weight. When the amount of water is less than the above range, it becomes difficult to use as a lotion type.
  • the amount of water (c) is 80.0% of the total amount of the cosmetic composition.
  • % For example, about 80.0 to 98.0% by weight, preferably about 85.5 to 94.5% by weight, and particularly preferably about 87.0 to 92.0% by weight. If the blending amount of water (c) exceeds the above range, the solubilizing power becomes insufficient, the transparency of the cosmetic composition tends to decrease, and the cleaning power tends to decrease. On the other hand, if the blending amount of water (c) is below the above range, the blending amount of the mono- or polyglycerin fatty acid ester (a2) is relatively increased, which is not only uneconomical, but also has a sticky feeling and skin irritation. There is a tendency that the feeling of use and safety decrease.
  • the blending amount of the mono- or polyglycerin alkyl or alkenyl ether (a1) is, for example, the total amount of the cosmetic composition It is 5.5 wt% or more and less than 9.0 wt%, preferably about 6.0 to 8.5 wt%, particularly preferably about 6.5 to 8.5 wt%. If the blending amount of mono- or polyglycerin alkyl or alkenyl ether is less than the above range, the solubilizing power is insufficient and the transparency of the cosmetic composition tends to be lowered.
  • the blending amount of mono- or polyglycerin alkyl or alkenyl ether exceeds the above range, not only is it uneconomical, but also stickiness and skin irritation increase, so that the feeling of use and safety tend to decrease.
  • the blending amount of the mono- or polyglycerin fatty acid ester (a2) is, for example, 1.0 to 10.0% by weight of the total amount of the cosmetic composition.
  • % Preferably about 3.0 to 7.5% by weight, particularly preferably about 4.5 to 7.5% by weight, and most preferably about 5.5 to 7.5% by weight.
  • the solubilizing power tends to be insufficient and the transparency of the cosmetic composition tends to be lowered.
  • blend it becomes difficult to mix
  • blend a sufficient quantity of oil-based component in order to ensure detergency, and there exists a tendency for detergency to fall.
  • the total amount of the cosmetic composition is 1.5% by weight or more and less than 5.0% by weight, preferably about 2.0 to 4.5% by weight, particularly preferably about 2.0 to 3.5% by weight. . If the blending amount of the silicone oil is below the above range, the detergency tends to decrease. On the other hand, when the blending amount of the silicone oil exceeds the above range, solubilization becomes difficult, and the transparency of the cosmetic composition tends to decrease. Also, the cleaning power tends to decrease.
  • the amount of the silicone oil (b) is, for example, the total amount of the cosmetic composition About 1.0 to 10.0% by weight, preferably about 2.5 to 7.0% by weight, particularly preferably about 3.5 to 5.5% by weight, most preferably 3.5 to 4.5% by weight Degree.
  • the blending amount of the silicone oil (b) is below the above range, the detergency tends to decrease.
  • the compounding quantity of silicone oil (b) exceeds the said range, solubilization will become difficult and there exists a tendency for the transparency of the composition for cosmetics to fall. Also, the cleaning power tends to decrease.
  • the amount of water (c) when using mono- or polyglycerin alkyl or alkenyl ether (a1) and mono- or polyglycerin fatty acid ester (a2) is the total amount of the cosmetic composition. Of 80.0% by weight or more, preferably about 80.0 to 90.0% by weight. When the amount of water is less than the above range, it becomes difficult to use as a lotion type.
  • the total amount of the mono- or polyglycerin alkyl or alkenyl ether (a1) and mono- or polyglycerin fatty acid ester (a2) used in the cosmetic composition of the present invention is, for example, 5 of the total amount of the cosmetic composition. It is about 0.0% by weight or more and less than 10.0% by weight, preferably about 5.5 to 9.5% by weight, particularly preferably about 6.0 to 9.0% by weight. If the blending amount of mono- or polyglycerin alkyl or alkenyl ether and mono- or polyglycerin fatty acid ester is below the above range, the solubilizing power tends to be insufficient and the transparency of the cosmetic composition tends to be lowered.
  • the amount of the silicone oil (b) when the mono- or polyglycerin alkyl or alkenyl ether (a1) and the mono- or polyglycerin fatty acid ester (a2) are used is, for example, cosmetics It is 1.0% by weight or more and less than 6.0% by weight, preferably about 2.0 to 5.0% by weight, particularly preferably about 3.0 to 4.0% by weight of the total amount of the composition for use. If the blending amount of the silicone oil is below the above range, the detergency tends to decrease. On the other hand, when the blending amount of the silicone oil exceeds the above range, solubilization becomes difficult, and the transparency of the cosmetic composition tends to decrease. Also, the cleaning power tends to decrease.
  • the cosmetic composition according to the present invention includes: Other additives such as amphoteric surfactants and nonionic surfactants may be blended. By blending these, the skin feel can be improved.
  • amphoteric surfactant is not particularly limited as long as it is used in a normal cosmetic composition, and examples thereof include carbobetaine-based active agents, amide betaine-based active agents, sulfobetaine-based active agents, Examples include betaine activators, imidazolium betaine activators, amine oxide activators, and the like.
  • the nonionic surfactant is not particularly limited as long as it is used in ordinary cosmetic compositions.
  • polyoxyethylene fatty acid ester polyoxyethylene hydrogenated castor oil, polyoxyethylene sorbitan Fatty acid ester, C 8-12 fatty acid monoglyceride, glycerin monoalkyl ether, polyoxyethylene alkyl ether, polyoxyethylene polyoxypropylene glycol, coconut oil fatty acid diethanolamide, C 6-24 fatty acid diethanolamide, C 6-24 fatty acid monoethanol
  • Examples thereof include amides and alkyl saccharide surfactants.
  • the cosmetic composition according to the present invention further includes components used in normal cosmetic compositions, for example, viscosity modifiers such as anionic, nonionic, and cationic polymers; moisturizing components such as polyols.
  • viscosity modifiers such as anionic, nonionic, and cationic polymers
  • moisturizing components such as polyols.
  • Oily components such as squalane, jojoba oil, olive oil, higher alcohols, lanolin, and esters; amides, foaming agents, preservatives, water-soluble polymers, pH adjusters, UV absorbers, pearling agents, antioxidants, and fragrances , Pigments and the like can be appropriately blended within a range not impairing the effects of the present invention.
  • the cosmetic composition of the present invention comprises the mono- or polyglycerin alkyl or alkenyl ether (a1) and / or mono- or polyglycerin fatty acid ester (a2), silicone oil (b), water (c) (for example, distilled water). , Purified water, industrial purified water, deionized water, and the like), and other additives as necessary.
  • the maximum particle size of micelles contained in the cosmetic composition of the present invention is, for example, 1 ⁇ m or less, preferably 500 nm or less, particularly preferably 100 nm or less.
  • the maximum particle size of the micelle can be measured using, for example, a nanotrack particle size analyzer.
  • the cosmetic composition according to the present invention contains silicone oil as an oil component, it has excellent detergency for highly hydrophobic cosmetics (for example, waterproof mascara, lipstick, foundation, etc.). Have. In addition, silicone oil does not have a sticky feeling peculiar to oily components, so it is excellent in use feeling. Further, the above mono- or polyglycerin alkyl or alkenyl ether and mono- or polyglycerin fatty acid ester used as a surfactant are hypoallergenic and have excellent solubilizing power. It is possible to form a lotion-type cosmetic composition having low irritation, high safety and transparency.
  • the cosmetic composition according to the present invention has excellent detergency, usability, safety, and beautiful appearance, and thus is useful as, for example, a cleansing lotion, a lotion, and the like.
  • the cosmetic composition according to the present invention when used as a cleansing lotion, for example, for use in wiping cosmetics (for example, cosmetics with high hydrophobicity such as waterproof mascara) contained in cotton or the like. It can be preferably used.
  • the skin after use is not sticky and does not need to be washed away. Therefore, it can be used even in the absence of water and can be used very easily.
  • Example A cosmetic composition was produced by a conventional method using the blending compositions (% by weight) shown in Tables 1 and 2 below, and the transparency and detergency were evaluated by the following methods.
  • the cosmetic composition according to the present invention contains, as an oily component, a silicone oil that does not have a sticky feeling peculiar to an oily component, so that it is an excellent cleaning agent for highly hydrophobic cosmetics such as a waterproof mascara. While having power, it has an excellent feeling of use without stickiness. Then, the silicone oil forms a stable micelle by the surface-active action of a hypoallergenic mono- or polyglycerin alkyl or alkenyl ether, or mono- or polyglycerin fatty acid ester, and is highly dispersed in water to form a microemulsion. Therefore, it has a transparent appearance and is excellent in safety. That is, the cosmetic composition according to the present invention can be suitably used as a cleansing lotion having excellent appearance and excellent detergency, safety and usability.

Abstract

This cosmetic composition contains a mono- or poly-glycerin alkyl or alkenyl ether (a1), and/or a mono or poly-glycerin fatty acid ester (a2), a silicone oil (b), and water (c), and is characterized in that the amount of water contained therein constitutes 80 wt% or more of the cosmetic composition. The mono- or poly-glycerin alkyl or alkenyl ether (a1) is preferably a mono- or poly-glycerin monoalkyl or alkenyl ether represented by formula (1). R1O-(C3H6O2)n1-H (1). (In the formula, R1 represents a C8-22 straight-chain or branched alkyl group or alkenyl group which may have a hydroxyl group. n1 represents the average degree of polymerization of the glycerin, and is 1-10.)

Description

化粧料用組成物Cosmetic composition
 本発明は、ローションタイプの化粧料用組成物に関する。 The present invention relates to a lotion type cosmetic composition.
 従来、ローションタイプの化粧料用組成物(例えば、クレンジングローション等)は、主に水分(通常、化粧料用組成物全量の70~90重量%程度配合)、油性成分、及び界面活性剤の3成分を配合したものが提供されていた。しかし、近年、消費者の間では、油性成分特有のべたつきが嫌われる傾向がある。その一方で、クレンジングローションには、ウォータープルーフ性マスカラ等の疎水性の高い化粧料の洗浄に使用することができる優れた洗浄力が求められている。 Conventionally, lotion-type cosmetic compositions (for example, cleansing lotions and the like) are mainly composed of water (usually about 70 to 90% by weight of the total amount of the cosmetic composition), an oily component, and a surfactant. A blend of ingredients was provided. However, in recent years, there is a tendency for consumers to dislike the stickiness peculiar to oil components. On the other hand, cleansing lotions are required to have excellent detergency that can be used for washing highly hydrophobic cosmetics such as waterproof mascara.
 化粧料用組成物のべたつきを解消する方法として、べたつきの原因となる油性成分を含有しないクレンジングローションが提供されるようになった。油性成分を含有しないクレンジングローションは、べたつきが無くさっぱりした使用感を有するが、洗浄力が低下する。洗浄力を向上させるために界面活性剤を増量すると、界面活性剤特有のべたつきが生じるだけでなく、皮膚刺激性が強まり炎症等を引き起こす恐れがある。そのため、洗浄力、使用感、及び安全性を兼ね備えることが困難であった。 As a method of eliminating the stickiness of cosmetic compositions, cleansing lotions that do not contain oily ingredients that cause stickiness have been provided. A cleansing lotion that does not contain an oil component has no stickiness and a refreshing feeling of use, but the cleaning power is reduced. When the amount of the surfactant is increased in order to improve the detergency, not only the stickiness peculiar to the surfactant is generated, but also the skin irritation becomes strong and may cause inflammation. For this reason, it is difficult to combine detergency, usability, and safety.
 一方で、シリコーンオイルは皮膚表面に塗布すると化粧料と容易に馴染み、化粧料を皮膚表面から速やかに浮き上がらせるという油性成分特有の性質は有するが、他の油性成分のようなべたつき感は無い。そこで、油性成分としてシリコーンオイルを配合した、べたつきが無く洗浄力に優れる化粧料用組成物の開発が行われていた。しかし、シリコーンオイルは水への可溶化が極めて困難であり、水と混合すると不透明の外観を呈し美観を損なうことから、ウォータープルーフ性マスカラ等の疎水性の高い化粧料に対して十分な洗浄力を発揮できる程度の量のシリコーンオイルを含有するローションタイプの化粧料用組成物を調製することは困難であった。 On the other hand, silicone oil is easily adapted to cosmetics when applied to the skin surface, and has a characteristic characteristic of oily components that allows the cosmetics to quickly rise from the skin surface, but does not feel sticky like other oily components. Therefore, development of a cosmetic composition having a non-stickiness and an excellent detergency, in which silicone oil is blended as an oil component has been performed. However, since silicone oil is extremely difficult to solubilize in water and mixes with water, it has an opaque appearance and impairs aesthetics.Therefore, it has sufficient detergency for highly hydrophobic cosmetics such as waterproof mascara. It has been difficult to prepare a lotion-type cosmetic composition containing an amount of silicone oil that is sufficient to exhibit the above.
 界面活性剤を増量することなくシリコーンオイルを可溶化する方法としては、界面活性剤と共にエタノールなどのアルコールを可溶化補助剤として使用する方法が知られている(特許文献1)。しかし、可溶化力の高いアルコール(例えば、エタノール)は刺激性が強いため、化粧料のへの配合には適さず、低刺激性のアルコール(例えば、1,3-ブチレングリコール等の多価アルコール)は自己組織化阻害能を生じミセルを形成しにくくするためやはり化粧料への配合には適さなかった。 As a method for solubilizing silicone oil without increasing the amount of surfactant, a method using an alcohol such as ethanol as a solubilizing aid together with a surfactant is known (Patent Document 1). However, alcohols with high solubilizing power (for example, ethanol) are highly irritating, so they are not suitable for blending into cosmetics. ) Is not suitable for blending into cosmetics because it has the ability to inhibit self-assembly and makes it difficult to form micelles.
特開2003-226617号公報JP 2003-226617 A
 従って、本発明の目的は、べたつきが無く使用感に優れ、且つ優れた洗浄力を有するローションタイプの透明化粧料用組成物を提供することにある。 Therefore, an object of the present invention is to provide a lotion-type transparent cosmetic composition having no stickiness, excellent usability, and excellent detergency.
 本発明者等は、上記課題を解決するため鋭意検討した結果、シリコーンオイルに特定の構造を有する低刺激性のモノ若しくはポリグリセリンアルキル又はアルケニルエーテル及び/又はモノ若しくはポリグリセリン脂肪酸エステルを添加すると、シリコーンオイルの水に対する溶解性を著しく向上させることができ、シリコーンオイルと水と前記界面活性剤を含有し、且つ前記水を80重量%以上含有する、低刺激性のローションタイプの化粧料用組成物を形成することができること、前記化粧料用組成物は、油性成分特有のべたつき感を有さないシリコーンオイルを油性成分として含有するため、ウォータープルーフ性マスカラ等の疎水性の高い化粧料に対して優れた洗浄力を有しつつ、べたつきが無く使用感が優れ、且つ、シリコーンオイルが界面活性剤によって安定なO/W型ミセル内部に包含され、水中に高分散されてマイクロエマルションを形成し、該分散状態が維持されるので、透明の外観を有することを見いだした。本発明はこれらの知見に基づいて完成させたものである。 As a result of intensive studies to solve the above problems, the present inventors have added hypoallergenic mono- or polyglycerin alkyl or alkenyl ether and / or mono- or polyglycerin fatty acid ester having a specific structure to the silicone oil. A low-irritant lotion-type cosmetic composition that can significantly improve the solubility of silicone oil in water, contains silicone oil, water, and the surfactant, and contains 80% by weight or more of the water. The cosmetic composition contains a silicone oil that does not have a sticky feeling peculiar to an oily component as an oily component, so that the cosmetic composition has a high hydrophobicity such as a waterproof mascara. Silicone with excellent detergency, no stickiness and excellent usability Yl is contained within a stable O / W type micelle by surfactant, it is highly dispersed to form a microemulsion in water, since the dispersion state is maintained, was found to have a transparent appearance. The present invention has been completed based on these findings.
 すなわち、本発明は、モノ若しくはポリグリセリンアルキル又はアルケニルエーテル(a1)及び/又はモノ若しくはポリグリセリン脂肪酸エステル(a2)、シリコーンオイル(b)、及び水(c)を含有する化粧料用組成物で、前記水の含有量が化粧料用組成物全量の80重量%以上であることを特徴とする化粧料用組成物を提供する。 That is, the present invention is a cosmetic composition containing mono- or polyglycerin alkyl or alkenyl ether (a1) and / or mono- or polyglycerin fatty acid ester (a2), silicone oil (b), and water (c). The cosmetic composition is characterized in that the water content is 80% by weight or more of the total amount of the cosmetic composition.
 前記モノ若しくはポリグリセリンアルキル又はアルケニルエーテル(a1)としては、下記式(1)
    R1O-(C362)n1-H       (1)
(式中、R1はヒドロキシル基を有していてもよい炭素数8~22の直鎖状若しくは分岐鎖状アルキル基又はアルケニル基を示す。n1はグリセリンの平均重合度を示し、1~10である)
で表されるモノ若しくはポリグリセリンモノアルキル又はアルケニルエーテルが好ましく、HLB値が8.0~12.0であることが好ましい。
As the mono- or polyglycerin alkyl or alkenyl ether (a1), the following formula (1)
R 1 O— (C 3 H 6 O 2 ) n 1 —H (1)
(In the formula, R 1 represents a linear or branched alkyl group or alkenyl group having 8 to 22 carbon atoms which may have a hydroxyl group. N 1 represents the average degree of polymerization of glycerin, 1 to 10)
The mono- or polyglycerin monoalkyl or alkenyl ether represented by the formula (1) is preferred, and the HLB value is preferably 8.0 to 12.0.
 前記モノ若しくはポリグリセリン脂肪酸エステル(a2)としては、下記式(2)
    R2C(=O)O-(C362)n2-H    (2)
(式中、R2はヒドロキシル基を有していてもよい炭素数8~22の直鎖状又は分岐鎖状脂肪族炭化水素基を示す。n2はグリセリンの平均重合度を示し、1~10である)
で表され、HLB値が9.0~15.0である化合物が好ましい。
As said mono- or polyglycerin fatty acid ester (a2), following formula (2)
R 2 C (═O) O— (C 3 H 6 O 2 ) n 2 —H (2)
(In the formula, R 2 represents a linear or branched aliphatic hydrocarbon group having 8 to 22 carbon atoms which may have a hydroxyl group. N 2 represents the average degree of polymerization of glycerin, 1 to 10)
And a compound having an HLB value of 9.0 to 15.0 is preferred.
 モノ若しくはポリグリセリン脂肪酸エステル(a2)を用いない場合、モノ若しくはポリグリセリンアルキル又はアルケニルエーテル(a1)、シリコーンオイル(b)、及び水(c)の化粧料用組成物全量に対する含有量としては、下記範囲であることが好ましい。
 モノ若しくはポリグリセリンアルキル又はアルケニルエーテル(a1):5.5重量%以上、9.0重量%未満
 シリコーンオイル(b):1.5重量%以上、5.0重量%未満
 水(c):86~93重量%
When the mono- or polyglycerin fatty acid ester (a2) is not used, the content of the mono- or polyglycerin alkyl or alkenyl ether (a1), silicone oil (b), and water (c) relative to the total amount of the cosmetic composition is: The following range is preferable.
Mono- or polyglycerin alkyl or alkenyl ether (a1): 5.5% by weight or more and less than 9.0% by weight Silicone oil (b): 1.5% by weight or more and less than 5.0% by weight Water (c): 86 ~ 93% by weight
 モノ若しくはポリグリセリンアルキル又はアルケニルエーテル(a1)を用いない場合、前記モノ若しくはポリグリセリン脂肪酸エステル(a2)、シリコーンオイル(b)、及び水(c)の化粧料用組成物全量に対する含有量としては、下記範囲であることが好ましい。
 モノ若しくはポリグリセリン脂肪酸エステル(a2):1.0~10.0重量%
 シリコーンオイル(b):1.0~10.0重量%
 水(c):80.0~98.0重量%
When the mono- or polyglycerin alkyl or alkenyl ether (a1) is not used, the content of the mono- or polyglycerin fatty acid ester (a2), silicone oil (b), and water (c) relative to the total amount of the cosmetic composition The following range is preferable.
Mono or polyglycerol fatty acid ester (a2): 1.0 to 10.0% by weight
Silicone oil (b): 1.0 to 10.0% by weight
Water (c): 80.0 to 98.0% by weight
 モノ若しくはポリグリセリンアルキル又はアルケニルエーテル(a1)及びモノ若しくはポリグリセリン脂肪酸エステル(a2)を用いる場合、モノ若しくはポリグリセリンアルキル又はアルケニルエーテル(a1)、モノ若しくはポリグリセリン脂肪酸エステル(a2)、シリコーンオイル、及び水の化粧料用組成物全量に対する含有量としては、下記範囲であることが好ましい。
 モノ若しくはポリグリセリンアルキル又はアルケニルエーテル(a1)及びモノ若しくはポリグリセリン脂肪酸エステル(a2):5.0重量%以上、10.0重量%未満
 シリコーンオイル(b):1.0重量%以上、6.0重量%未満
 水(c):80.0重量%以上
When using mono or polyglycerol alkyl or alkenyl ether (a1) and mono or polyglycerol fatty acid ester (a2), mono or polyglycerol alkyl or alkenyl ether (a1), mono or polyglycerol fatty acid ester (a2), silicone oil, And as content with respect to the cosmetics composition whole quantity of water, it is preferable that it is the following range.
Mono- or polyglycerin alkyl or alkenyl ether (a1) and mono- or polyglycerin fatty acid ester (a2): 5.0% by weight or more and less than 10.0% by weight Silicone oil (b): 1.0% by weight or more, 6. Less than 0% by weight Water (c): 80.0% by weight or more
 本発明に係る化粧料用組成物は、油性成分として、油性成分特有のべたつき感を有さないシリコーンオイルを含有するため、ウォータープルーフ性マスカラ等の疎水性の高い化粧料に対して優れた洗浄力を有しつつ、べたつきの無い優れた使用感を有する。そして、低刺激性のモノ若しくはポリグリセリンアルキル又はアルケニルエーテル及び/又はモノ若しくはポリグリセリン脂肪酸エステルの界面活性作用により前記シリコーンオイルが安定なミセルを形成して水中に高分散され、マイクロエマルションを形成することができるので、透明の外観を有し、且つ、安全性に優れる。すなわち、発明に係る化粧料用組成物は、外観に優れ、洗浄力、安全性及び使用感に優れたクレンジングローションとして好適に使用することができる。 The cosmetic composition according to the present invention contains, as an oil component, a silicone oil that does not have a sticky feeling peculiar to an oil component, so that it is excellent for highly hydrophobic cosmetics such as a waterproof mascara. While having power, it has an excellent feeling of use without stickiness. Then, the silicone oil forms a stable micelle by the surface active action of hypoallergenic mono- or polyglyceryl alkyl or alkenyl ether and / or mono- or polyglycerin fatty acid ester, and is highly dispersed in water to form a microemulsion. Therefore, it has a transparent appearance and is excellent in safety. That is, the cosmetic composition according to the present invention can be suitably used as a cleansing lotion having an excellent appearance and an excellent detergency, safety and usability.
 [モノ若しくはポリグリセリンアルキル又はアルケニルエーテル(a1)]
 本発明の化粧料用組成物は、界面活性剤として刺激性が低く安全性に優れるモノ若しくはポリグリセリンアルキル又はアルケニルエーテル(a1)及び/又はモノ若しくはポリグリセリン脂肪酸エステル(a2)を使用する。モノ若しくはポリグリセリンアルキル又はアルケニルエーテル(a1)としては、モノグリセリンモノアルキル又はアルケニルエーテル、モノグリセリンジアルキル又はアルケニルエーテル、ポリグリセリンモノアルキル又はアルケニルエーテル、及びポリグリセリンジアルキル又はアルケニルエーテル等を挙げることができる。
[Mono or polyglycerin alkyl or alkenyl ether (a1)]
The cosmetic composition of the present invention uses a mono- or polyglycerin alkyl or alkenyl ether (a1) and / or a mono- or polyglycerin fatty acid ester (a2) that is low in irritation and excellent in safety as a surfactant. Examples of the mono- or polyglycerin alkyl or alkenyl ether (a1) include monoglycerin monoalkyl or alkenyl ether, monoglycerin dialkyl or alkenyl ether, polyglycerin monoalkyl or alkenyl ether, and polyglycerin dialkyl or alkenyl ether. .
 本発明においては、なかでも、下記式(1)表されるモノ若しくはポリグリセリンモノアルキル又はアルケニルエーテルが、疎水性の強いシリコーンオイルを水へ可溶化する力(可溶化力)に優れる点で好ましい。式(1)中、R1はヒドロキシル基を有していてもよい炭素数8~22の直鎖状若しくは分岐鎖状アルキル基又はアルケニル基を示す。n1はグリセリンの平均重合度を示し、1~10である。
    R1O-(C362)n1-H       (1)
In the present invention, among them, mono- or polyglycerin monoalkyl or alkenyl ether represented by the following formula (1) is preferable in that it has excellent power (solubilization power) for solubilizing highly hydrophobic silicone oil in water. . In the formula (1), R 1 represents a linear or branched alkyl group or alkenyl group having 8 to 22 carbon atoms which may have a hydroxyl group. n 1 represents an average degree of polymerization of glycerin and is 1 to 10.
R 1 O— (C 3 H 6 O 2 ) n 1 —H (1)
 式(1)の括弧内のC362は、下記式(3)及び(4)で示される両方の構造を有する。
  -CH2-CHOH-CH2O-    (3)
  -CH(CH2OH)CH2O-    (4)
C 3 H 6 O 2 in parentheses in the formula (1) has both structures represented by the following formulas (3) and (4).
—CH 2 —CHOH—CH 2 O— (3)
—CH (CH 2 OH) CH 2 O— (4)
 式(1)中、R1はヒドロキシル基を有していてもよい炭素数8~22の直鎖状若しくは分岐鎖状アルキル基又はアルケニル基を示す。炭素数8~22の直鎖状アルキル基としては、例えば、n-オクチル、n-ノニル、n-デシル、n-ウンデシル、n-ラウリル、n-トリデシル、n-テトラデシル、n-ペンタデシル、n-パルミチル、n-ヘプタデシル、n-ステアリル、n-ノナデシル、n-エイコシル、n-ヘンエイコシル、n-ドコシル基等を挙げることができる。炭素数8~22の直鎖状アルケニル基としては、例えば、n-オクテニル、n-ノネニル、n-デセニル、n-ウンデセニル、n-ドデセニル、n-トリデセニル、n-テトラデセニル、n-ペンタデセニル、n-ヘキサデセニル、n-ヘプタデセニル、n-エライジル、n-オレイル、n-ノナデセニル、n-ガドレイル、n-エイコセニル、n-ヘンエイコセニル、n-ドコセニル基等を挙げることができる。 In the formula (1), R 1 represents a linear or branched alkyl group or alkenyl group having 8 to 22 carbon atoms which may have a hydroxyl group. Examples of the linear alkyl group having 8 to 22 carbon atoms include n-octyl, n-nonyl, n-decyl, n-undecyl, n-lauryl, n-tridecyl, n-tetradecyl, n-pentadecyl, n- Examples include palmityl, n-heptadecyl, n-stearyl, n-nonadecyl, n-eicosyl, n-heneicosyl, n-docosyl group and the like. Examples of the linear alkenyl group having 8 to 22 carbon atoms include n-octenyl, n-nonenyl, n-decenyl, n-undecenyl, n-dodecenyl, n-tridecenyl, n-tetradecenyl, n-pentadecenyl, n- Examples include hexadecenyl, n-heptadecenyl, n-eylidyl, n-oleyl, n-nonadecenyl, n-gadoleyl, n-eicosenyl, n-heneicosenyl, n-docosenyl and the like.
 ヒドロキシル基を有する炭素数8~22の直鎖状アルキル基又はアルケニル基としては、上記炭素数8~22の直鎖状アルキル基又はアルケニル基の1個以上の水素原子がヒドロキシル基で置換された基を挙げることができる。 As the linear alkyl group or alkenyl group having 8 to 22 carbon atoms and having a hydroxyl group, one or more hydrogen atoms of the linear alkyl group or alkenyl group having 8 to 22 carbon atoms are substituted with a hydroxyl group. The group can be mentioned.
 炭素数8~22の分岐鎖状アルキル基としては、例えば、イソオクチル、s-オクチル、t-オクチル、イソノニル、s-ノニル、t-ノニル、イソデシル、s-デシル、t-デシル、イソウンデシル、s-ウンデシル、t-ウンデシル、イソラウリル、s-ラウリル、t-ラウリル、イソトリデシル、s-トリデシル、t-トリデシル、イソテトラデシル、s-テトラデシル、t-テトラデシル、イソペンタデシル、s-ペンタデシル、t-ペンタデシル、イソパルミチル、2-ヘキシルデシル、s-パルミチル、t-パルミチル、イソヘプタデシル、s-ヘプタデシル、t-ヘプタデシル、イソステアリル、s-ステアリル、t-ステアリル、イソノナデシル、s-ノナデシル、t-ノナデシル、2-オクチルラウリル、イソエイコシル、s-エイコシル、t-エイコシル、イソヘンエイコシル、s-ヘンエイコシル、t-ヘンエイコシル、イソドコシル、s-ドコシル、t-ドコシル基等を挙げることができる。炭素数8~22の分岐鎖状アルケニル基としては、例えば、イソオクテニル、s-オクテニル、t-オクテニル、イソノネニル、s-ノネニル、t-ノネニル、イソデセニル、s-デセニル、t-デセニル、イソウンデセニル、s-ウンデセニル、t-ウンデセニル、イソドデセニル、s-ドデセニル、t-ドデセニル、イソトリデセニル、s-トリデセニル、t-トリデセニル、イソテトラデセニル、s-テトラデセニル、t-テトラデセニル、イソペンタデセニル、s-ペンタデセニル、t-ペンタデセニル、イソヘキサデセニル、s-ヘキサデセニル、t-ヘキサデセニル、イソヘプタデセニル、s-ヘプタデセニル、t-ヘプタデセニル、イソオレイル、s-オレイル、t-オレイル、イソノナデセニル、s-ノナデセニル、t-ノナデセニル、イソエイコセニル、s-エイコセニル、t-エイコセニル、イソヘンエイコセニル、s-ヘンエイコセニル、t-ヘンエイコセニル、イソドコセニル、s-ドコセニル、t-ドコセニル基等を挙げることができる。 Examples of the branched alkyl group having 8 to 22 carbon atoms include isooctyl, s-octyl, t-octyl, isononyl, s-nonyl, t-nonyl, isodecyl, s-decyl, t-decyl, isoundecyl, s- Undecyl, t-undecyl, isolauryl, s-lauryl, t-lauryl, isotridecyl, s-tridecyl, t-tridecyl, isotetradecyl, s-tetradecyl, t-tetradecyl, isopentadecyl, s-pentadecyl, t-pentadecyl, Isopalmityl, 2-hexyldecyl, s-palmityl, t-palmityl, isoheptadecyl, s-heptadecyl, t-heptadecyl, isostearyl, s-stearyl, t-stearyl, isononadecyl, s-nonadecyl, t-nonadecyl, 2-octyllauryl , Isoeikoshi , S- eicosyl, t-eicosyl, iso Heng eicosyl, s- heneicosyl, t-heneicosyl, Isodokoshiru, s- docosyl, t-docosyl group and the like. Examples of the branched alkenyl group having 8 to 22 carbon atoms include isooctenyl, s-octenyl, t-octenyl, isononenyl, s-nonenyl, t-nonenyl, isodecenyl, s-decenyl, t-decenyl, isoundecenyl, s- Undecenyl, t-undecenyl, isododecenyl, s-dodecenyl, t-dodecenyl, isotridecenyl, s-tridecenyl, t-tridecenyl, isotetradecenyl, s-tetradecenyl, t-tetradecenyl, isopentadecenyl, s-pentadecenyl, t-pentadecenyl, isohexadecenyl, s-hexadecenyl, t-hexadecenyl, isoheptadecenyl, s-heptadecenyl, t-heptadecenyl, isooleyl, s-oleyl, t-oleyl, isononadecenyl, s-nonadecenyl, t- No Decenyl, Isoeikoseniru, s- eicosenyl, t-eicosenyl, iso Heng Eiko cell alkenyl, s- heneicosenyl, t-heneicosenyl, Isodokoseniru, s- docosenyl, may be mentioned t-docosenyl group.
 ヒドロキシル基を有する炭素数8~22の分岐鎖状アルキル基又はアルケニル基としては、上記炭素数8~22の分岐鎖状アルキル基又はアルケニル基の1個以上の水素原子がヒドロキシル基で置換された基を挙げることができる。 As the branched alkyl group or alkenyl group having 8 to 22 carbon atoms having a hydroxyl group, one or more hydrogen atoms of the branched alkyl group or alkenyl group having 8 to 22 carbon atoms is substituted with a hydroxyl group. The group can be mentioned.
 式(1)で表されるモノ若しくはポリグリセリンモノアルキル又はアルケニルエーテルとしては、なかでも、水溶性が高く、シリコーンオイルの可溶化力に優れる点で、R1が、炭素数8~22の直鎖状若しくは分岐鎖状アルキル基であることが好ましく、特に、n-ラウリル基、n-ミリスチル基等の炭素数8~22(特に炭素数12~14)の直鎖状アルキル基が好ましい。 As the mono- or polyglycerin monoalkyl or alkenyl ether represented by the formula (1), R 1 is a straight chain having 8 to 22 carbon atoms because it has high water solubility and excellent solubilizing power of silicone oil. A linear or branched alkyl group is preferable, and a linear alkyl group having 8 to 22 carbon atoms (particularly 12 to 14 carbon atoms) such as an n-lauryl group or an n-myristyl group is particularly preferable.
 式(1)中、n1はグリセリンの平均重合度を示し、例えば1~10、好ましくは1~5、特に好ましくは1~3である。n1の値が1を下回ると疎水性が高まり、水に対する可溶化力が低下する傾向がある。一方、n1の値が10を上回ると親水性が高まり、シリコーンオイルに対する可溶化力が低下する傾向がある。 In the formula (1), n 1 represents an average degree of polymerization of glycerin, and is, for example, 1 to 10, preferably 1 to 5, particularly preferably 1 to 3. When the value of n 1 is less than 1, the hydrophobicity increases and the water solubilizing power tends to decrease. On the other hand, when the value of n 1 exceeds 10, hydrophilicity tends to increase and solubilizing power to silicone oil tends to decrease.
 上記式(1)で表されるモノ若しくはポリグリセリンモノアルキル又はアルケニルエーテル(a1)の製造方法としては、特に限定されるものではないが、例えば、塩基性触媒の存在下、脂肪族アルコールに、該アルコールとグリシドールの存在比(モル比)が特定の値となるようにグリシドールを添加して反応させる方法;モノ若しくはポリグリセリンにα-オレフィンエポキシドを反応させる方法;酸触媒もしくはアルカリ触媒の存在下でアルキルグリシジルエーテルを、モノ若しくはポリグリセリンを用いて開環させる方法等が挙げられる。 The production method of the mono- or polyglycerin monoalkyl or alkenyl ether (a1) represented by the above formula (1) is not particularly limited. For example, in the presence of a basic catalyst, A method in which glycidol is added and reacted so that the abundance ratio (molar ratio) of the alcohol and glycidol is a specific value; a method in which an α-olefin epoxide is reacted with mono- or polyglycerin; in the presence of an acid catalyst or an alkali catalyst And a method of opening a ring of alkyl glycidyl ether using mono- or polyglycerin.
 本発明におけるモノ若しくはポリグリセリンアルキル又はアルケニルエーテル(a1)のHLB値としては、例えば8.0~12.0、好ましくは9.0~11.0、特に好ましくは9.5以上、11.0未満である。HLB値が上記範囲を下回ると、疎水性が高くなりすぎ、モノ若しくはポリグリセリンアルキル又はアルケニルエーテルがシリコーンオイルにのみ溶解し、水への溶解が困難となる傾向があり、マイクロエマルションの形成が困難となる傾向がある。一方、HLB値が上記範囲を上回ると親水性が高くなりすぎ、モノ若しくはポリグリセリンアルキル又はアルケニルエーテルが水にのみ溶解し、シリコーンオイルへの溶解が困難となる傾向があり、マイクロエマルションの形成が困難となる傾向がある。HLB値は、例えば、アルキル基又はアルケニル基の炭素数を多くすることでHLB値を下げ、またポリグリセリンの重合度を上げるとHLB値を上げることができる。そのため、以上の分子構造を制御することによりHLB値を調整することができる。 The HLB value of the mono- or polyglycerin alkyl or alkenyl ether (a1) in the present invention is, for example, 8.0 to 12.0, preferably 9.0 to 11.0, particularly preferably 9.5 or more, 11.0. Is less than. When the HLB value is below the above range, the hydrophobicity becomes too high, and mono- or polyglycerin alkyl or alkenyl ether dissolves only in silicone oil, and it tends to be difficult to dissolve in water, making it difficult to form a microemulsion. Tend to be. On the other hand, when the HLB value exceeds the above range, the hydrophilicity becomes too high, mono- or polyglycerin alkyl or alkenyl ether is dissolved only in water, and it tends to be difficult to dissolve in silicone oil. It tends to be difficult. For example, the HLB value can be decreased by increasing the number of carbon atoms of the alkyl group or alkenyl group, and can be increased by increasing the degree of polymerization of polyglycerol. Therefore, the HLB value can be adjusted by controlling the above molecular structure.
 本発明におけるモノ若しくはポリグリセリンアルキル又はアルケニルエーテル(a1)の好ましい例としては、モノグリセリンモノラウリルエーテル(HLB値:8.5)、ジグリセリンモノラウリルエーテル(HLB値:10.6)、トリグリセリンモノミリスチルエーテル(HLB値:11.0)等を挙げることができる。これらは単独で、又は2種以上を組み合わせて使用することができる。 Preferred examples of the mono- or polyglycerin alkyl or alkenyl ether (a1) in the present invention include monoglycerin monolauryl ether (HLB value: 8.5), diglycerin monolauryl ether (HLB value: 10.6), triglycerin. And monomyristyl ether (HLB value: 11.0). These can be used alone or in combination of two or more.
 [モノ若しくはポリグリセリン脂肪酸エステル(a2)]
 本発明の化粧料用組成物は、界面活性剤として刺激性が低く安全性に優れるモノ若しくはポリグリセリンアルキル又はアルケニルエーテル(a1)及び/又はモノ若しくはポリグリセリン脂肪酸エステル(a2)を使用する。前記モノ若しくはポリグリセリン脂肪酸エステル(a2)は、下記式(2)表される。式(2)中、R2はヒドロキシル基を有していてもよい炭素数8~22の直鎖状又は分岐鎖状脂肪族炭化水素基を示す。n2はグリセリンの平均重合度を示し、1~10である。
    R2C(=O)O-(C362)n2-H    (2)
[Mono or polyglycerol fatty acid ester (a2)]
The cosmetic composition of the present invention uses a mono- or polyglycerin alkyl or alkenyl ether (a1) and / or a mono- or polyglycerin fatty acid ester (a2) that is low in irritation and excellent in safety as a surfactant. The mono- or polyglycerin fatty acid ester (a2) is represented by the following formula (2). In the formula (2), R 2 represents a linear or branched aliphatic hydrocarbon group having 8 to 22 carbon atoms which may have a hydroxyl group. n 2 represents the average degree of polymerization of glycerin and is 1 to 10.
R 2 C (═O) O— (C 3 H 6 O 2 ) n 2 —H (2)
 式(2)の括弧内のC362は、下記式(5)及び(6)で示される両方の構造を有する。
  -CH2-CHOH-CH2O-    (5)
  -CH(CH2OH)CH2O-    (6)
C 3 H 6 O 2 in parentheses in the formula (2) has both structures represented by the following formulas (5) and (6).
—CH 2 —CHOH—CH 2 O— (5)
—CH (CH 2 OH) CH 2 O— (6)
 式(2)中、R2はヒドロキシル基を有していてもよい炭素数8~22の直鎖状又は分岐鎖状脂肪族炭化水素基を示す。炭素数8~22の直鎖状脂肪族炭化水素基としては、例えば、n-オクチル、n-ノニル、n-デシル、n-ウンデシル、n-ラウリル、n-トリデシル、n-テトラデシル、n-ペンタデシル、n-パルミチル、n-ヘプタデシル、n-ステアリル、n-ノナデシル、n-エイコシル、n-ヘンエイコシル、n-ドコシル基等のC8-22直鎖アルキル基;n-オクテニル、n-ノネニル、n-デセニル、n-ウンデセニル、n-ドデセニル、n-トリデセニル、n-テトラデセニル、n-ペンタデセニル、n-ヘキサデセニル、n-ヘプタデセニル、n-エライジル、n-オレイル、n-ノナデセニル、n-ガドレイル、n-エイコセニル、n-ヘンエイコセニル、n-ドコセニル基等のC8-22直鎖アルケニル基等を挙げることができる。 In the formula (2), R 2 represents a linear or branched aliphatic hydrocarbon group having 8 to 22 carbon atoms which may have a hydroxyl group. Examples of the linear aliphatic hydrocarbon group having 8 to 22 carbon atoms include n-octyl, n-nonyl, n-decyl, n-undecyl, n-lauryl, n-tridecyl, n-tetradecyl, and n-pentadecyl. C 8-22 straight chain alkyl groups such as n-palmityl, n-heptadecyl, n-stearyl, n-nonadecyl, n-eicosyl, n-heneicosyl, n-docosyl; n-octenyl, n-nonenyl, n- Decenyl, n-undecenyl, n-dodecenyl, n-tridecenyl, n-tetradecenyl, n-pentadecenyl, n-hexadecenyl, n-heptadecenyl, n-elaidyl, n-oleyl, n-nonadecenyl, n-gadoleyl, n-eicosenyl, Examples thereof include C 8-22 straight chain alkenyl groups such as n-heneicosenyl and n-docosenyl groups.
 ヒドロキシル基を有する炭素数8~22の直鎖状脂肪族炭化水素基としては、上記炭素数8~22の直鎖状脂肪族炭化水素基の1個以上の水素原子がヒドロキシル基で置換された基を挙げることができる。 As the linear aliphatic hydrocarbon group having 8 to 22 carbon atoms and having a hydroxyl group, one or more hydrogen atoms of the above linear aliphatic hydrocarbon group having 8 to 22 carbon atoms are substituted with a hydroxyl group. The group can be mentioned.
 炭素数8~22の分岐鎖状脂肪族炭化水素基としては、例えば、イソオクチル、s-オクチル、t-オクチル、イソノニル、s-ノニル、t-ノニル、イソデシル、s-デシル、t-デシル、イソウンデシル、s-ウンデシル、t-ウンデシル、イソラウリル、s-ラウリル、t-ラウリル、イソトリデシル、s-トリデシル、t-トリデシル、イソテトラデシル、s-テトラデシル、t-テトラデシル、イソペンタデシル、s-ペンタデシル、t-ペンタデシル、イソパルミチル、2-ヘキシルデシル、s-パルミチル、t-パルミチル、イソヘプタデシル、s-ヘプタデシル、t-ヘプタデシル、イソステアリル、s-ステアリル、t-ステアリル、イソノナデシル、s-ノナデシル、t-ノナデシル、2-オクチルラウリル、イソエイコシル、s-エイコシル、t-エイコシル、イソヘンエイコシル、s-ヘンエイコシル、t-ヘンエイコシル、イソドコシル、s-ドコシル、t-ドコシル基等のC8-22分岐アルキル基;イソオクテニル、s-オクテニル、t-オクテニル、イソノネニル、s-ノネニル、t-ノネニル、イソデセニル、s-デセニル、t-デセニル、イソウンデセニル、s-ウンデセニル、t-ウンデセニル、イソドデセニル、s-ドデセニル、t-ドデセニル、イソトリデセニル、s-トリデセニル、t-トリデセニル、イソテトラデセニル、s-テトラデセニル、t-テトラデセニル、イソペンタデセニル、s-ペンタデセニル、t-ペンタデセニル、イソヘキサデセニル、s-ヘキサデセニル、t-ヘキサデセニル、イソヘプタデセニル、s-ヘプタデセニル、t-ヘプタデセニル、イソオレイル、s-オレイル、t-オレイル、イソノナデセニル、s-ノナデセニル、t-ノナデセニル、イソエイコセニル、s-エイコセニル、t-エイコセニル、イソヘンエイコセニル、s-ヘンエイコセニル、t-ヘンエイコセニル、イソドコセニル、s-ドコセニル、t-ドコセニル基等のC8-22分岐アルケニル基等を挙げることができる。 Examples of the branched aliphatic hydrocarbon group having 8 to 22 carbon atoms include isooctyl, s-octyl, t-octyl, isononyl, s-nonyl, t-nonyl, isodecyl, s-decyl, t-decyl, and isoundecyl. , S-undecyl, t-undecyl, isolauryl, s-lauryl, t-lauryl, isotridecyl, s-tridecyl, t-tridecyl, isotetradecyl, s-tetradecyl, t-tetradecyl, isopentadecyl, s-pentadecyl, t -Pentadecyl, isopalmityl, 2-hexyldecyl, s-palmityl, t-palmityl, isoheptadecyl, s-heptadecyl, t-heptadecyl, isostearyl, s-stearyl, t-stearyl, isononadecyl, s-nonadecyl, t-nonadecyl, 2 -Octyl lauryl, iso ray Sill, s- eicosyl, t-eicosyl, iso Heng eicosyl, s- heneicosyl, t-heneicosyl, Isodokoshiru, s- docosyl, C 8-22 branched alkyl group such as t-docosyl group; isooctenyl, s- octenyl, t -Octenyl, isononenyl, s-nonenyl, t-nonenyl, isodecenyl, s-decenyl, t-decenyl, isoundecenyl, s-undecenyl, t-undecenyl, isododecenyl, s-dodecenyl, t-dodecenyl, isotridecenyl, s-tridecenyl, t -Tridecenyl, isotetradecenyl, s-tetradecenyl, t-tetradecenyl, isopentadecenyl, s-pentadecenyl, t-pentadecenyl, isohexadecenyl, s-hexadecenyl, t-hexadecenyl, isoheptadecenyl , S-heptade Senyl, t-heptadecenyl, isooleyl, s-oleyl, t-oleyl, isononadecenyl, s-nonadecenyl, t-nonadecenyl, isoeicosenyl, s-eicosenyl, t-eicosenyl, isoheneicosenyl, s-heneicosenyl, t-henecocenyl, Examples thereof include C 8-22 branched alkenyl groups such as isodocosenyl, s-docosenyl, and t-docosenyl groups.
 ヒドロキシル基を有する炭素数8~22の分岐鎖状脂肪族炭化水素基としては、上記炭素数8~22の分岐鎖状脂肪族炭化水素基の1個以上の水素原子がヒドロキシル基で置換された基を挙げることができる。 As the branched aliphatic hydrocarbon group having 8 to 22 carbon atoms and having a hydroxyl group, one or more hydrogen atoms of the branched aliphatic hydrocarbon group having 8 to 22 carbon atoms are substituted with a hydroxyl group. The group can be mentioned.
 本発明のモノ若しくはポリグリセリン脂肪酸エステル(a2)としては、なかでも、シリコーンオイルの可溶化力に優れる点で、式(2)中のR2が、炭素数8~22の直鎖状又は分岐鎖状アルキル基であることが好ましく、特に、特に、n-ラウリル基、n-ミリスチル基等の炭素数8~22(特に炭素数12~14)の直鎖状アルキル基であることが好ましい。 As the mono- or polyglycerin fatty acid ester (a2) of the present invention, R 2 in the formula (2) is a linear or branched group having 8 to 22 carbon atoms, particularly in terms of the excellent solubilizing power of silicone oil. A chain alkyl group is preferable, and a linear alkyl group having 8 to 22 carbon atoms (particularly 12 to 14 carbon atoms) such as an n-lauryl group and an n-myristyl group is particularly preferable.
 式(2)中、n2はグリセリンの平均重合度を示し、例えば1~10、好ましくは1~5、特に好ましくは1~3である。n2の値が1を下回ると疎水性が高まり、水に対する可溶化力が低下する傾向がある。一方、n2の値が10を上回ると親水性が高まり、シリコーンオイルに対する可溶化力が低下する傾向がある。 In the formula (2), n 2 represents the average degree of polymerization of glycerin, and is, for example, 1 to 10, preferably 1 to 5, and particularly preferably 1 to 3. When the value of n 2 is less than 1, the hydrophobicity increases and the water solubilizing power tends to decrease. On the other hand, when the value of n 2 exceeds 10, hydrophilicity tends to increase and solubilizing power to silicone oil tends to decrease.
 本発明におけるモノ若しくはポリグリセリン脂肪酸エステル(a2)のHLB値としては、例えば9.0~15.0、好ましくは9.0~13.0、特に好ましくは9.0~12.0である。HLB値が上記範囲を下回ると、疎水性が高くなりすぎ、モノ若しくはポリグリセリン脂肪酸エステルがシリコーンオイルにのみ溶解し、水への溶解が困難となる傾向がある。一方、HLB値が上記範囲を上回ると、親水性が高くなりすぎ、モノ若しくはポリグリセリン脂肪酸エステルが水にのみ可溶し、シリコーンオイルへの溶解が困難となる傾向がある。HLB値は、例えば、脂肪酸残基の炭素数を多くすることでHLB値を下げ、またポリグリセリンの重合度を上げるとHLB値を上げることができる。そのため、以上の分子構造を制御することによりHLB値を調整することができる。 The HLB value of the mono- or polyglycerin fatty acid ester (a2) in the present invention is, for example, 9.0 to 15.0, preferably 9.0 to 13.0, and particularly preferably 9.0 to 12.0. When the HLB value is less than the above range, the hydrophobicity becomes too high, and the mono- or polyglycerin fatty acid ester tends to dissolve only in the silicone oil, making it difficult to dissolve in water. On the other hand, when the HLB value exceeds the above range, the hydrophilicity becomes too high, and the mono- or polyglycerin fatty acid ester tends to be soluble only in water and difficult to dissolve in silicone oil. For example, the HLB value can be increased by increasing the number of carbon atoms of the fatty acid residue, and can be increased by increasing the polymerization degree of the polyglycerol. Therefore, the HLB value can be adjusted by controlling the above molecular structure.
 本発明におけるモノ若しくはポリグリセリン脂肪酸エステル(a2)の好ましい例としては、ジグリセリンモノラウレート、ジグリセリンモノミリステート等を挙げることができる。これらは単独で、又は2種以上を組み合わせて使用することができる。 Preferred examples of the mono- or polyglycerin fatty acid ester (a2) in the present invention include diglycerin monolaurate and diglycerin monomyristate. These can be used alone or in combination of two or more.
 本発明においては、例えば、商品名「ポエム DL-100」(ジグリセリンモノラウレート、HLB:9.4、理研ビタミン(株)製)、商品名「ポエム DM-100」(ジグリセリンモノミリスチレート、HLB:10.1、理研ビタミン(株)製)等の市販品を好適に使用することができる。 In the present invention, for example, the trade name “Poem DL-100” (diglycerin monolaurate, HLB: 9.4, manufactured by Riken Vitamin Co., Ltd.), the trade name “Poem DM-100” (diglycerin monomyristate). Commercial products such as rate, HLB: 10.1, manufactured by Riken Vitamin Co., Ltd. can be preferably used.
 [シリコーンオイル(b)]
 本発明のシリコーンオイル(b)としては、少なくとも、主鎖がシロキサン結合からなるポリシロキサンであればよく、主鎖の末端及び/又は側鎖に置換基を有していてもよい。また、前記主鎖は、環を形成していてもよい。シリコーンオイル(b)には、ストレートシリコーンオイル及び変性シリコーンオイルが含まれる。
[Silicone oil (b)]
The silicone oil (b) of the present invention may be at least a polysiloxane having a main chain composed of a siloxane bond, and may have a substituent at the end of the main chain and / or the side chain. The main chain may form a ring. Silicone oil (b) includes straight silicone oil and modified silicone oil.
 前記ストレートシリコーンオイルは、主鎖がシロキサン結合からなるポリシロキサンであり、置換基を有する場合、置換基はメチル基及び/又はフェニル基であり、メチル基、フェニル基以外の置換基は有さない。 The straight silicone oil is a polysiloxane whose main chain is composed of a siloxane bond, and when it has a substituent, the substituent is a methyl group and / or a phenyl group, and has no substituent other than a methyl group and a phenyl group. .
 ストレートシリコーンオイルにおける置換基の結合位置は特に限定されず、主鎖の両末端(両末端型:下記式(7)で表される)又は片末端(片末端型:下記式(8)で表される)に有していてもよいし、側鎖(側鎖型:下記式(9)で表される)に有していてもよく、側鎖及び両末端に置換基を有していてもよく(側鎖及び両末端型:下記式(10)で表される)、さらに、側鎖及び片末端に置換基を有していてもよい(側鎖及び片末端型:下記式(11)で表される)。全ての側鎖及び末端がメチル基で置換されていてもよい(下記式(12)で表される)。下記式(9)~(11)で表される化合物は、ランダム共重合体、交互共重合体、ブロック共重合体等の何れであってもよい。 The bonding position of the substituent in the straight silicone oil is not particularly limited, and both ends of the main chain (both ends type: represented by the following formula (7)) or one end (one end type: represented by the following formula (8) May be present on the side chain (side chain type: represented by the following formula (9)), and has a substituent on the side chain and both ends. In addition, the side chain and both terminal types: represented by the following formula (10) may further have a substituent on the side chain and one terminal (side chain and one terminal type: the following formula (11) )). All side chains and terminals may be substituted with methyl groups (represented by the following formula (12)). The compounds represented by the following formulas (9) to (11) may be any of random copolymers, alternating copolymers, block copolymers and the like.
Figure JPOXMLDOC01-appb-C000001
Figure JPOXMLDOC01-appb-C000001
 上記式中のX1、X2、X3は水素原子又はフェニル基であり、m、nは、1以上の整数である。X1、X2、X3は、それぞれ同一であってもよく異なっていてもよい。m、nもまた、同一であってもよく異なっていてもよい。 X 1 , X 2 and X 3 in the above formula are a hydrogen atom or a phenyl group, and m and n are integers of 1 or more. X 1 , X 2 and X 3 may be the same or different. m and n may also be the same or different.
 ストレートシリコーンオイルの具体例としては、全ての側鎖、末端がメチル基からなるジメチルシリコーン、及び前記ジメチルシリコーンが環を形成して成る環状ジメチルシリコーン、側鎖の一部にフェニル基を含むメチルフェニルシリコーン、側鎖の一部が水素であるメチルハイドロジェンシリコーン等を挙げることができる。本発明においては、なかでも、シクロペンタシロキサン、ジフェニルシロキシフェニルトリメチコン等が、優れた洗浄力を有しつつ、より一層べたつき感が少ない点で好ましく、例えば、商品名「FK-995」(シクロペンタシロキサン、信越シリコーン(株)製)、商品名「KF-56A」(ジフェニルシロキシフェニルトリメチコン、信越シリコーン(株)製)等の市販品を好適に使用することができる。 Specific examples of the straight silicone oil include all side chains, dimethyl silicone having a terminal methyl group, and cyclic dimethyl silicone in which the dimethyl silicone forms a ring, methyl phenyl having a phenyl group in a part of the side chain. Examples thereof include silicone and methyl hydrogen silicone in which a part of the side chain is hydrogen. In the present invention, among them, cyclopentasiloxane, diphenylsiloxyphenyl trimethicone and the like are preferable because they have excellent detergency and less stickiness. For example, the trade name “FK-995” (cyclohexane) Commercially available products such as pentasiloxane, manufactured by Shin-Etsu Silicone Co., Ltd., and trade name “KF-56A” (diphenylsiloxyphenyl trimethicone, manufactured by Shin-Etsu Silicone Co., Ltd.) can be suitably used.
 変性シリコーンオイルは、主鎖がシロキサン結合からなるポリシロキサンであり、メチル基、フェニル基以外の置換基を有するものである。変性シリコーンオイルにおける前記置換基の結合位置は特に限定されず、主鎖の両末端(両末端型:下記式(13)で表される)又は片末端(片末端型:下記式(14)で表される)に有していてもよいし、側鎖(側鎖型:下記式(15)で表される)に有していてもよく、側鎖及び両末端に置換基を有していてもよく(側鎖及び両末端型:下記式(16)で表される)、さらに、側鎖及び片末端に置換基を有していてもよい(側鎖及び片末端型:下記式(17)で表される)。下記式(15)~(17)で表される化合物は、ランダム共重合体、交互共重合体、ブロック共重合体等の何れであってもよい。 The modified silicone oil is a polysiloxane whose main chain is composed of a siloxane bond, and has a substituent other than a methyl group and a phenyl group. The bonding position of the substituent in the modified silicone oil is not particularly limited, and both ends of the main chain (both ends type: represented by the following formula (13)) or one end (one end type: the following formula (14) May be present in the side chain (side chain type: represented by the following formula (15)), and has a substituent on the side chain and at both ends. (A side chain and both terminal types: represented by the following formula (16)), and may further have a substituent on the side chain and one terminal (side chain and one terminal type: the following formula ( 17)). The compounds represented by the following formulas (15) to (17) may be any of random copolymers, alternating copolymers, block copolymers and the like.
Figure JPOXMLDOC01-appb-C000002
Figure JPOXMLDOC01-appb-C000002
 上記式中のX4、X5、X6は置換基(メチル基、フェニル基以外)であり、m'、n'は、1以上の整数である。X4、X5、X6は、それぞれ同一であってもよく異なっていてもよい。m'、n'もまた、同一であってもよく異なっていてもよい。 In the above formula, X 4 , X 5 and X 6 are substituents (other than methyl group and phenyl group), and m ′ and n ′ are integers of 1 or more. X 4 , X 5 and X 6 may be the same or different. m ′ and n ′ may also be the same or different.
 上記式中のX4、X5、X6におけるメチル基、フェニル基以外の置換基としては、例えば、炭素数2以上のアルキル基、アラルキル基、エポキシ基、フッ素原子、アミノ基、カルボキシル基、脂肪族ヒドロキシル基(アルコール性水酸基)、フェニル基以外の芳香族ヒドロキシル基(フェノール性水酸基)、(メタ)アクリロイル基含有の置換基、ポリエーテル鎖を含有する置換基等を挙げることができる。 Examples of the substituent other than the methyl group and the phenyl group in X 4 , X 5 and X 6 in the above formula include, for example, an alkyl group having 2 or more carbon atoms, an aralkyl group, an epoxy group, a fluorine atom, an amino group, a carboxyl group, Examples include aliphatic hydroxyl groups (alcoholic hydroxyl groups), aromatic hydroxyl groups other than phenyl groups (phenolic hydroxyl groups), (meth) acryloyl group-containing substituents, substituents containing polyether chains, and the like.
 本発明における変性シリコーンオイルとしては、なかでも、置換基として炭素数2以上のアルキル基を有する変性シリコーンオイルが、洗浄力をより向上させることができる点で好ましく、特に、置換基として炭素数8~18の直鎖状若しくは分岐鎖状アルキル基(例えば、ラウリル基、セチル基等)を側鎖に有する変性シリコーンオイルが好ましい。本発明においては、例えば、商品名「SS-3408」(カプリリルメチコン、東レ・ダウコーニング(株)製)、「2502 Cosmetic Fluid」(セチルジメチコン、東レ・ダウコーニング(株)製)等の市販品を好適に使用することができる。 As the modified silicone oil in the present invention, among them, a modified silicone oil having an alkyl group having 2 or more carbon atoms as a substituent is preferable in that it can further improve the detergency. Modified silicone oils having 18 to 18 linear or branched alkyl groups (for example, lauryl group, cetyl group, etc.) in the side chain are preferred. In the present invention, for example, commercial names such as “SS-3408” (caprylylmethicone, manufactured by Toray Dow Corning) and “2502 Cosmetic Fluid” (cetyl dimethicone, manufactured by Toray Dow Corning) are commercially available. The product can be suitably used.
 本発明におけるシリコーンオイルとしては、例えば、商品名「KF-995」(シクロペンタシロキサン、信越シリコーン(株)製)、商品名「KF-56A」(ジフェニルシロキシフェニルトリメチコン、信越シリコーン(株)製)等のストレートシリコーンオイルや、商品名「SS-3408」(カプリリルメチコン、東レ・ダウコーニング(株)製)、「2502 Cosmetic Fluid」(セチルジメチコン、東レ・ダウコーニング(株)製)等の側鎖型アルキル変性シリコーンオイル等を好適に使用することができる。これらは単独で、又は2種以上を組み合わせて使用することができる。 As the silicone oil in the present invention, for example, trade name “KF-995” (cyclopentasiloxane, manufactured by Shin-Etsu Silicone Co., Ltd.), trade name “KF-56A” (diphenylsiloxyphenyl trimethicone, manufactured by Shin-Etsu Silicone Co., Ltd.) ), Etc., trade names such as “SS-3408” (caprylyl methicone, manufactured by Toray Dow Corning Co., Ltd.), “2502 Cosmetic Fluid” (cetyl dimethicone, manufactured by Toray Dow Corning Co., Ltd.), etc. A side chain type alkyl-modified silicone oil or the like can be preferably used. These can be used alone or in combination of two or more.
 [化粧料用組成物]
 本発明の化粧料用組成物は、モノ若しくはポリグリセリンアルキル又はアルケニルエーテル(a1)及び/又はモノ若しくはポリグリセリン脂肪酸エステル(a2)、シリコーンオイル(b)、及び水(c)を含有する化粧料用組成物で、前記水の含有量が化粧料用組成物全量の80.0重量%以上であることを特徴とする。
[Cosmetic composition]
The cosmetic composition of the present invention comprises a mono- or polyglycerin alkyl or alkenyl ether (a1) and / or a mono- or polyglycerin fatty acid ester (a2), a silicone oil (b), and water (c). The water content is 80.0% by weight or more of the total amount of the cosmetic composition.
 本発明の化粧料用組成物において、モノ若しくはポリグリセリン脂肪酸エステル(a2)を用いず、モノ若しくはポリグリセリンアルキル又はアルケニルエーテル(a1)を用いる場合の水(c)の配合量は、化粧料用組成物全量の80.0重量%以上であり、好ましくは86.0~93.0重量%程度である。水の配合量が上記範囲を下回ると、ローションタイプとしての使用が困難となる。
 また、モノ若しくはポリグリセリンアルキル又はアルケニルエーテル(a1)を用いず、モノ若しくはポリグリセリン脂肪酸エステル(a2)を用いる場合の水(c)の配合量は、化粧料用組成物全量の80.0重量%以上であり、例えば80.0~98.0重量%程度、好ましくは85.5~94.5重量%程度、特に好ましくは87.0~92.0重量%程度である。水(c)の配合量が上記範囲を上回ると、可溶化力が不十分となり化粧料用組成物の透明性が低下し、洗浄力が低下する傾向がある。一方、水(c)の配合量が上記範囲を下回ると、モノ若しくはポリグリセリン脂肪酸エステル(a2)の配合量が相対的に増加するため、不経済であるばかりでなく、べたつき感及び皮膚刺激性が増加し、使用感及び安全性が低下する傾向がある。
In the cosmetic composition of the present invention, when the mono- or polyglycerin fatty acid ester (a2) is not used and the mono- or polyglycerin alkyl or alkenyl ether (a1) is used, It is 80.0% by weight or more of the total amount of the composition, preferably about 86.0 to 93.0% by weight. When the amount of water is less than the above range, it becomes difficult to use as a lotion type.
In addition, when mono or polyglycerin alkyl or alkenyl ether (a1) is not used and mono or polyglycerin fatty acid ester (a2) is used, the amount of water (c) is 80.0% of the total amount of the cosmetic composition. %, For example, about 80.0 to 98.0% by weight, preferably about 85.5 to 94.5% by weight, and particularly preferably about 87.0 to 92.0% by weight. If the blending amount of water (c) exceeds the above range, the solubilizing power becomes insufficient, the transparency of the cosmetic composition tends to decrease, and the cleaning power tends to decrease. On the other hand, if the blending amount of water (c) is below the above range, the blending amount of the mono- or polyglycerin fatty acid ester (a2) is relatively increased, which is not only uneconomical, but also has a sticky feeling and skin irritation. There is a tendency that the feeling of use and safety decrease.
 本発明の化粧料用組成物において、モノ若しくはポリグリセリン脂肪酸エステル(a2)を用いない場合、モノ若しくはポリグリセリンアルキル又はアルケニルエーテル(a1)の配合量としては、例えば、化粧料用組成物全量の5.5重量%以上、9.0重量%未満、好ましくは6.0~8.5重量%程度、特に好ましくは6.5~8.5重量%程度である。モノ若しくはポリグリセリンアルキル又はアルケニルエーテルの配合量が上記範囲を下回ると、可溶化力が不十分となり化粧料用組成物の透明性が低下する傾向がある。また、洗浄力を確保するために十分な量の油性成分を配合することが困難となり、洗浄力が低下する傾向がある。一方、モノ若しくはポリグリセリンアルキル又はアルケニルエーテルの配合量が上記範囲を上回ると、不経済であるばかりでなく、べたつき感及び皮膚刺激性が増加するため、使用感及び安全性が低下する傾向がある。
 また、モノ若しくはポリグリセリンアルキル又はアルケニルエーテル(a1)を用いない場合、モノ若しくはポリグリセリン脂肪酸エステル(a2)の配合量としては、例えば、化粧料用組成物全量の1.0~10.0重量%程度、好ましくは3.0~7.5重量%程度、特に好ましくは4.5~7.5重量%程度、最も好ましくは5.5~7.5重量%程度である。モノ若しくはポリグリセリン脂肪酸エステル(a2)の配合量が上記範囲を下回ると、可溶化力が不十分となり化粧料用組成物の透明性が低下する傾向がある。また、洗浄力を確保するために十分な量の油性成分を配合することが困難となり、洗浄力が低下する傾向がある。一方、モノ若しくはポリグリセリン脂肪酸エステル(a2)の配合量が上記範囲を上回ると、不経済であるばかりでなく、べたつき感及び皮膚刺激性が増加し、使用感及び安全性が低下する傾向がある。
When the mono- or polyglycerin fatty acid ester (a2) is not used in the cosmetic composition of the present invention, the blending amount of the mono- or polyglycerin alkyl or alkenyl ether (a1) is, for example, the total amount of the cosmetic composition It is 5.5 wt% or more and less than 9.0 wt%, preferably about 6.0 to 8.5 wt%, particularly preferably about 6.5 to 8.5 wt%. If the blending amount of mono- or polyglycerin alkyl or alkenyl ether is less than the above range, the solubilizing power is insufficient and the transparency of the cosmetic composition tends to be lowered. Moreover, it becomes difficult to mix | blend a sufficient quantity of oil-based component in order to ensure detergency, and there exists a tendency for detergency to fall. On the other hand, when the blending amount of mono- or polyglycerin alkyl or alkenyl ether exceeds the above range, not only is it uneconomical, but also stickiness and skin irritation increase, so that the feeling of use and safety tend to decrease. .
When the mono- or polyglycerin alkyl or alkenyl ether (a1) is not used, the blending amount of the mono- or polyglycerin fatty acid ester (a2) is, for example, 1.0 to 10.0% by weight of the total amount of the cosmetic composition. %, Preferably about 3.0 to 7.5% by weight, particularly preferably about 4.5 to 7.5% by weight, and most preferably about 5.5 to 7.5% by weight. When the blending amount of the mono- or polyglycerin fatty acid ester (a2) is less than the above range, the solubilizing power tends to be insufficient and the transparency of the cosmetic composition tends to be lowered. Moreover, it becomes difficult to mix | blend a sufficient quantity of oil-based component in order to ensure detergency, and there exists a tendency for detergency to fall. On the other hand, when the blending amount of the mono- or polyglycerin fatty acid ester (a2) exceeds the above range, not only is it uneconomical, but also stickiness and skin irritation increase, and the feeling of use and safety tend to decrease. .
 本発明の化粧料用組成物において、モノ若しくはポリグリセリン脂肪酸エステル(a2)を用いず、モノ若しくはポリグリセリンアルキル又はアルケニルエーテル(a1)を用いる場合のシリコーンオイル(b)の配合量としては、例えば、化粧料用組成物全量の1.5重量%以上、5.0重量%未満、好ましくは2.0~4.5重量%程度、特に好ましくは2.0~3.5重量%程度である。シリコーンオイルの配合量が上記範囲を下回ると、洗浄力が低下する傾向がある。一方、シリコーンオイルの配合量が上記範囲を上回ると、可溶化が困難となり、化粧料用組成物の透明性が低下する傾向がある。また、洗浄力も低下する傾向がある。
 また、モノ若しくはポリグリセリンアルキル又はアルケニルエーテル(a1)を用いず、モノ若しくはポリグリセリン脂肪酸エステル(a2)を用いる場合のシリコーンオイル(b)の配合量としては、例えば、化粧料用組成物全量の1.0~10.0重量%程度、好ましくは2.5~7.0重量%程度、特に好ましくは3.5~5.5重量%程度、最も好ましくは3.5~4.5重量%程度である。シリコーンオイル(b)の配合量が上記範囲を下回ると、洗浄力が低下する傾向がある。一方、シリコーンオイル(b)の配合量が上記範囲を上回ると、可溶化が困難となり、化粧料用組成物の透明性が低下する傾向がある。また、洗浄力も低下する傾向がある。
In the cosmetic composition of the present invention, when the mono- or polyglycerin fatty acid ester (a2) is not used and the mono- or polyglycerin alkyl or alkenyl ether (a1) is used, The total amount of the cosmetic composition is 1.5% by weight or more and less than 5.0% by weight, preferably about 2.0 to 4.5% by weight, particularly preferably about 2.0 to 3.5% by weight. . If the blending amount of the silicone oil is below the above range, the detergency tends to decrease. On the other hand, when the blending amount of the silicone oil exceeds the above range, solubilization becomes difficult, and the transparency of the cosmetic composition tends to decrease. Also, the cleaning power tends to decrease.
In addition, when the mono- or polyglycerin alkyl or alkenyl ether (a1) is not used and the mono- or polyglycerin fatty acid ester (a2) is used, the amount of the silicone oil (b) is, for example, the total amount of the cosmetic composition About 1.0 to 10.0% by weight, preferably about 2.5 to 7.0% by weight, particularly preferably about 3.5 to 5.5% by weight, most preferably 3.5 to 4.5% by weight Degree. When the blending amount of the silicone oil (b) is below the above range, the detergency tends to decrease. On the other hand, when the compounding quantity of silicone oil (b) exceeds the said range, solubilization will become difficult and there exists a tendency for the transparency of the composition for cosmetics to fall. Also, the cleaning power tends to decrease.
 本発明の化粧料用組成物において、モノ若しくはポリグリセリンアルキル又はアルケニルエーテル(a1)及びモノ若しくはポリグリセリン脂肪酸エステル(a2)を用いる場合の水(c)の配合量は、化粧料用組成物全量の80.0重量%以上であり、好ましくは80.0~90.0重量%程度である。水の配合量が上記範囲を下回ると、ローションタイプとしての使用が困難となる。 In the cosmetic composition of the present invention, the amount of water (c) when using mono- or polyglycerin alkyl or alkenyl ether (a1) and mono- or polyglycerin fatty acid ester (a2) is the total amount of the cosmetic composition. Of 80.0% by weight or more, preferably about 80.0 to 90.0% by weight. When the amount of water is less than the above range, it becomes difficult to use as a lotion type.
 本発明の化粧料用組成物においてモノ若しくはポリグリセリンアルキル又はアルケニルエーテル(a1)及びモノ若しくはポリグリセリン脂肪酸エステル(a2)を用いる場合の総配合量としては、例えば、化粧料用組成物全量の5.0重量%以上、10.0重量%未満、好ましくは5.5~9.5重量%程度、特に好ましくは6.0~9.0重量%程度である。モノ若しくはポリグリセリンアルキル又はアルケニルエーテル及びモノ若しくはポリグリセリン脂肪酸エステルの配合量が上記範囲を下回ると、可溶化力が不十分となり化粧料用組成物の透明性が低下する傾向がある。また、洗浄力を確保するために十分な量の油性成分を配合することが困難となり、洗浄力が低下する傾向がある。一方、モノ若しくはポリグリセリンアルキル又はアルケニルエーテル及びモノ若しくはポリグリセリン脂肪酸エステルの配合量が上記範囲を上回ると、不経済であるばかりでなく、べたつき感及び皮膚刺激性が増加するため、使用感及び安全性が低下する傾向がある。 The total amount of the mono- or polyglycerin alkyl or alkenyl ether (a1) and mono- or polyglycerin fatty acid ester (a2) used in the cosmetic composition of the present invention is, for example, 5 of the total amount of the cosmetic composition. It is about 0.0% by weight or more and less than 10.0% by weight, preferably about 5.5 to 9.5% by weight, particularly preferably about 6.0 to 9.0% by weight. If the blending amount of mono- or polyglycerin alkyl or alkenyl ether and mono- or polyglycerin fatty acid ester is below the above range, the solubilizing power tends to be insufficient and the transparency of the cosmetic composition tends to be lowered. Moreover, it becomes difficult to mix | blend a sufficient quantity of oil-based component in order to ensure detergency, and there exists a tendency for detergency to fall. On the other hand, when the amount of mono- or polyglycerin alkyl or alkenyl ether and mono- or polyglycerin fatty acid ester exceeds the above range, not only is it uneconomical, but also stickiness and skin irritation increase. Tend to decrease.
 本発明の化粧料用組成物において、モノ若しくはポリグリセリンアルキル又はアルケニルエーテル(a1)及びモノ若しくはポリグリセリン脂肪酸エステル(a2)を用いる場合のシリコーンオイル(b)の配合量としては、例えば、化粧料用組成物全量の1.0重量%以上、6.0重量%未満、好ましくは2.0~5.0重量%程度、特に好ましくは3.0~4.0重量%程度である。シリコーンオイルの配合量が上記範囲を下回ると、洗浄力が低下する傾向がある。一方、シリコーンオイルの配合量が上記範囲を上回ると、可溶化が困難となり、化粧料用組成物の透明性が低下する傾向がある。また、洗浄力も低下する傾向がある。 In the cosmetic composition of the present invention, the amount of the silicone oil (b) when the mono- or polyglycerin alkyl or alkenyl ether (a1) and the mono- or polyglycerin fatty acid ester (a2) are used is, for example, cosmetics It is 1.0% by weight or more and less than 6.0% by weight, preferably about 2.0 to 5.0% by weight, particularly preferably about 3.0 to 4.0% by weight of the total amount of the composition for use. If the blending amount of the silicone oil is below the above range, the detergency tends to decrease. On the other hand, when the blending amount of the silicone oil exceeds the above range, solubilization becomes difficult, and the transparency of the cosmetic composition tends to decrease. Also, the cleaning power tends to decrease.
 本発明に係る化粧料用組成物には、モノ若しくはポリグリセリンアルキル又はアルケニルエーテル(a1)及び/又はモノ若しくはポリグリセリン脂肪酸エステル(a2)、シリコーンオイル(b)、及び水(c)以外に、他の添加物、例えば、両性界面活性剤、非イオン性界面活性剤を配合してもよい。これらを配合することにより、肌感触を向上させることができる。 In addition to mono- or polyglycerin alkyl or alkenyl ether (a1) and / or mono- or polyglycerin fatty acid ester (a2), silicone oil (b), and water (c), the cosmetic composition according to the present invention includes: Other additives such as amphoteric surfactants and nonionic surfactants may be blended. By blending these, the skin feel can be improved.
 両性界面活性剤としては、通常の化粧料用組成物に用いられるものであれば特に制限されることがなく、例えば、カルボベタイン系活性剤、アミドベタイン系活性剤、スルホベタイン系活性剤、ホスホベタイン系活性剤、イミダゾリウムベタイン系活性剤、アミンオキサイド系活性剤等を挙げることができる。 The amphoteric surfactant is not particularly limited as long as it is used in a normal cosmetic composition, and examples thereof include carbobetaine-based active agents, amide betaine-based active agents, sulfobetaine-based active agents, Examples include betaine activators, imidazolium betaine activators, amine oxide activators, and the like.
 非イオン性界面活性剤としては、通常の化粧料用組成物に用いられるものであれば特に制限されることがなく、例えば、ポリオキシエチレン脂肪酸エステル、ポリオキシエチレン硬化ヒマシ油、ポリオキシエチレンソルビタン脂肪酸エステル、C8-12脂肪酸モノグリセリド、グリセリンモノアルキルエーテル、ポリオキシエチレンアルキルエーテル、ポリオキシエチレンポリオキシプロピレングリコール、ヤシ油脂肪酸ジエタノールアミド、C6-24脂肪酸ジエタノールアミド、C6-24脂肪酸モノエタノールアミド、アルキルサッカライド系界面活性剤等を挙げることができる。 The nonionic surfactant is not particularly limited as long as it is used in ordinary cosmetic compositions. For example, polyoxyethylene fatty acid ester, polyoxyethylene hydrogenated castor oil, polyoxyethylene sorbitan Fatty acid ester, C 8-12 fatty acid monoglyceride, glycerin monoalkyl ether, polyoxyethylene alkyl ether, polyoxyethylene polyoxypropylene glycol, coconut oil fatty acid diethanolamide, C 6-24 fatty acid diethanolamide, C 6-24 fatty acid monoethanol Examples thereof include amides and alkyl saccharide surfactants.
 本発明に係る化粧料用組成物には、更にまた、通常の化粧料用組成物に用いられる成分、例えば、アニオン性、ノニオン性、カチオン性ポリマー等の粘度調整剤;ポリオール類等の保湿成分;スクワラン、ホホバ油、オリーブ油、高級アルコール、ラノリン、エステル等の油性成分;アミド、増泡剤、防腐剤、水溶性高分子、pH調整剤、紫外線吸収剤、パール化剤、酸化防止剤、香料、色素等を、本発明の効果を損なわない範囲で適宜配合することができる。 The cosmetic composition according to the present invention further includes components used in normal cosmetic compositions, for example, viscosity modifiers such as anionic, nonionic, and cationic polymers; moisturizing components such as polyols. Oily components such as squalane, jojoba oil, olive oil, higher alcohols, lanolin, and esters; amides, foaming agents, preservatives, water-soluble polymers, pH adjusters, UV absorbers, pearling agents, antioxidants, and fragrances , Pigments and the like can be appropriately blended within a range not impairing the effects of the present invention.
 本発明の化粧料用組成物は、上記モノ若しくはポリグリセリンアルキル又はアルケニルエーテル(a1)及び/又はモノ若しくはポリグリセリン脂肪酸エステル(a2)、シリコーンオイル(b)、水(c)(例えば、蒸留水、精製水、工業用精製水、脱イオン水等)、及び必要に応じて他の添加物を混合、撹拌することにより製造することができる。 The cosmetic composition of the present invention comprises the mono- or polyglycerin alkyl or alkenyl ether (a1) and / or mono- or polyglycerin fatty acid ester (a2), silicone oil (b), water (c) (for example, distilled water). , Purified water, industrial purified water, deionized water, and the like), and other additives as necessary.
 本発明の化粧料用組成物では、モノ若しくはポリグリセリンアルキル又はアルケニルエーテル(a1)及び/又はモノ若しくはポリグリセリン脂肪酸エステル(a2)の界面活性作用により、シリコーンオイルを高含有し、粒度が極めて小さいミセルが形成され、シリコーンオイルが水中に高分散されるため[=水中油型(O/W型)マイクロエマルションを形成するため]、透明性を有し外観が美しい化粧料用組成物が得られる。 The cosmetic composition of the present invention contains a high amount of silicone oil and a very small particle size due to the surfactant activity of mono- or polyglycerin alkyl or alkenyl ether (a1) and / or mono- or polyglycerin fatty acid ester (a2). Since micelles are formed and silicone oil is highly dispersed in water [= to form an oil-in-water (O / W) microemulsion], a cosmetic composition having transparency and a beautiful appearance is obtained. .
 本発明の化粧料用組成物中に含有するミセルの最大粒度としては、例えば、1μm以下、好ましくは500nm以下、特に好ましくは100nm以下である。尚、前記ミセルの最大粒度は、例えばナノトラック粒度分析計を使用して測定することができる。 The maximum particle size of micelles contained in the cosmetic composition of the present invention is, for example, 1 μm or less, preferably 500 nm or less, particularly preferably 100 nm or less. The maximum particle size of the micelle can be measured using, for example, a nanotrack particle size analyzer.
 また、本発明に係る化粧料用組成物は、油性成分としてシリコーンオイルを含有するため、疎水性の高い化粧料(例えば、ウォータープルーフ性マスカラ、口紅、ファンデーション等)に対して優れた洗浄力を有する。その上、シリコーンオイルは油性成分特有のべたつき感がないため、使用感にも優れる。更に、界面活性剤として使用する上記モノ若しくはポリグリセリンアルキル又はアルケニルエーテル及びモノ若しくはポリグリセリン脂肪酸エステルは、低刺激性であり、その上、可溶化力に優れるため、少量の使用でシリコーンオイルを水に可溶化することができ、低刺激性で安全性が高く、透明性を有するローションタイプの化粧料用組成物を形成することができる。本発明に係る化粧料用組成物は優れた洗浄力、使用感、安全性、及び美しい外観を兼ね備えるため、例えば、クレンジングローション、化粧水等として有用である。 In addition, since the cosmetic composition according to the present invention contains silicone oil as an oil component, it has excellent detergency for highly hydrophobic cosmetics (for example, waterproof mascara, lipstick, foundation, etc.). Have. In addition, silicone oil does not have a sticky feeling peculiar to oily components, so it is excellent in use feeling. Further, the above mono- or polyglycerin alkyl or alkenyl ether and mono- or polyglycerin fatty acid ester used as a surfactant are hypoallergenic and have excellent solubilizing power. It is possible to form a lotion-type cosmetic composition having low irritation, high safety and transparency. The cosmetic composition according to the present invention has excellent detergency, usability, safety, and beautiful appearance, and thus is useful as, for example, a cleansing lotion, a lotion, and the like.
 特に、本発明に係る化粧料用組成物をクレンジングローションとして使用する場合、例えば、コットン等に含ませて化粧料(例えば、ウォータープルーフ性マスカラ等の疎水性の高い化粧料)を拭き取る用途等に好適に使用することができる。使用後の肌はべたつき感が無く、洗い流す必要がない。そのため、水が無いところでも使用することができ、非常に手軽に使用可能である。 In particular, when the cosmetic composition according to the present invention is used as a cleansing lotion, for example, for use in wiping cosmetics (for example, cosmetics with high hydrophobicity such as waterproof mascara) contained in cotton or the like. It can be preferably used. The skin after use is not sticky and does not need to be washed away. Therefore, it can be used even in the absence of water and can be used very easily.
 以下、実施例により本発明をより具体的に説明するが、本発明はこれらの実施例により限定されるものではない。 Hereinafter, the present invention will be described more specifically with reference to examples, but the present invention is not limited to these examples.
 実施例
 下記表1及び2に示す配合組成(重量%)により化粧料用組成物を常法により製造し、透明性、及び洗浄力を下記方法で評価した。
Example A cosmetic composition was produced by a conventional method using the blending compositions (% by weight) shown in Tables 1 and 2 below, and the transparency and detergency were evaluated by the following methods.
 [透明性]
 実施例で得られた各化粧料用組成物の粒度分布をナノトラック粒度分析計(商品名「UPA-EX150/UPA-EX-250」、日機装株式会社製)を使用して測定し、透明性を下記基準に従って評価した。
 評価基準
 ○:最大粒度が100nm以下
 △:最大粒度が100nmを超え、10μm未満
 ×:最大粒度が10μm以上
[transparency]
The particle size distribution of each cosmetic composition obtained in the examples was measured using a nanotrack particle size analyzer (trade name “UPA-EX150 / UPA-EX-250”, manufactured by Nikkiso Co., Ltd.), and the transparency Were evaluated according to the following criteria.
Evaluation criteria ○: Maximum particle size is 100 nm or less △: Maximum particle size exceeds 100 nm and less than 10 μm ×: Maximum particle size is 10 μm or more
 [洗浄力]
 上腕部にマスカラ(商品名「ボリューム エクスプレス ターボ ブースト N ウォータープルーフ(ブラック)」、メイベリン ニューヨーク製)0.1gを塗布し、30分間、ドライヤーを使用して乾燥させた。
 実施例で得られた各化粧料用組成物 2mLをコットンに染み込ませ、上腕部に塗布したマスカラに1分間馴染ませた後、5回拭き取り、マスカラの落ち度合いから洗浄力を下記基準に従って評価した。
 評価基準
 ○:完全に落ちた
 △:ほぼ落ちた
 ×:落ちが不十分であった
[Detergency]
Mascara (trade name “Volume Express Turbo Boost N Waterproof (Black)”, manufactured by Maybelline New York) 0.1 g was applied to the upper arm and dried using a dryer for 30 minutes.
Each cosmetic composition 2 mL obtained in the Examples was soaked in cotton and allowed to acclimate to the mascara applied to the upper arm for 1 minute, then wiped off 5 times, and the detergency was evaluated from the degree of mascara drop according to the following criteria. .
Evaluation criteria ○: Completely dropped △: Almost dropped ×: Drop was insufficient
 上記結果を下記表1及び2にまとめて示す。
Figure JPOXMLDOC01-appb-T000003
The above results are summarized in Tables 1 and 2 below.
Figure JPOXMLDOC01-appb-T000003
Figure JPOXMLDOC01-appb-T000004
Figure JPOXMLDOC01-appb-T000004
 本発明に係る化粧料用組成物は、油性成分として、油性成分特有のべたつき感を有さないシリコーンオイルを含有するため、ウォータープルーフ性マスカラ等の疎水性の高い化粧料に対して優れた洗浄力を有しつつ、べたつきの無い優れた使用感を有する。そして、低刺激性のモノ若しくはポリグリセリンアルキル又はアルケニルエーテル、又はモノ若しくはポリグリセリン脂肪酸エステルの界面活性作用により前記シリコーンオイルが安定なミセルを形成して水中に高分散され、マイクロエマルションを形成することができるので、透明の外観を有し、且つ、安全性に優れる。すなわち、発明に係る化粧料用組成物は、外観に優れ、洗浄力、安全性及び使用感に優れたクレンジングローションとして好適に使用することができる。 The cosmetic composition according to the present invention contains, as an oily component, a silicone oil that does not have a sticky feeling peculiar to an oily component, so that it is an excellent cleaning agent for highly hydrophobic cosmetics such as a waterproof mascara. While having power, it has an excellent feeling of use without stickiness. Then, the silicone oil forms a stable micelle by the surface-active action of a hypoallergenic mono- or polyglycerin alkyl or alkenyl ether, or mono- or polyglycerin fatty acid ester, and is highly dispersed in water to form a microemulsion. Therefore, it has a transparent appearance and is excellent in safety. That is, the cosmetic composition according to the present invention can be suitably used as a cleansing lotion having excellent appearance and excellent detergency, safety and usability.

Claims (7)

  1.  モノ若しくはポリグリセリンアルキル又はアルケニルエーテル(a1)及び/又はモノ若しくはポリグリセリン脂肪酸エステル(a2)、シリコーンオイル(b)、及び水(c)を含有する化粧料用組成物で、前記水の含有量が化粧料用組成物全量の80重量%以上であることを特徴とする化粧料用組成物。 A cosmetic composition containing mono- or polyglycerin alkyl or alkenyl ether (a1) and / or mono- or polyglycerin fatty acid ester (a2), silicone oil (b), and water (c), the water content Is a cosmetic composition, characterized in that is 80% by weight or more of the total amount of the cosmetic composition.
  2.  モノ若しくはポリグリセリンアルキル又はアルケニルエーテル(a1)が、下記式(1)
        R1O-(C362)n1-H       (1)
    (式中、R1はヒドロキシル基を有していてもよい炭素数8~22の直鎖状若しくは分岐鎖状アルキル基又はアルケニル基を示す。n1はグリセリンの平均重合度を示し、1~10である)
    で表されるモノ若しくはポリグリセリンモノアルキル又はアルケニルエーテルである請求項1に記載の化粧料用組成物。
    Mono- or polyglycerin alkyl or alkenyl ether (a1) is represented by the following formula (1)
    R 1 O— (C 3 H 6 O 2 ) n 1 —H (1)
    (In the formula, R 1 represents a linear or branched alkyl group or alkenyl group having 8 to 22 carbon atoms which may have a hydroxyl group. N 1 represents the average degree of polymerization of glycerol and 1 to 10)
    The cosmetic composition according to claim 1, which is a mono- or polyglycerin monoalkyl or alkenyl ether represented by the formula:
  3.  モノ若しくはポリグリセリンアルキル又はアルケニルエーテル(a1)のHLB値が8.0~12.0である請求項1又は2に記載の化粧料用組成物。 The cosmetic composition according to claim 1 or 2, wherein the mono- or polyglycerin alkyl or alkenyl ether (a1) has an HLB value of 8.0 to 12.0.
  4.  モノ若しくはポリグリセリン脂肪酸エステル(a2)が、下記式(2)
        R2C(=O)O-(C362)n2-H    (2)
    (式中、R2はヒドロキシル基を有していてもよい炭素数8~22の直鎖状又は分岐鎖状脂肪族炭化水素基を示す。n2はグリセリンの平均重合度を示し、1~10である)
    で表され、HLB値が9.0~15.0である化合物である請求項1に記載の化粧料用組成物。
    Mono- or polyglycerin fatty acid ester (a2) is represented by the following formula (2)
    R 2 C (═O) O— (C 3 H 6 O 2 ) n 2 —H (2)
    (In the formula, R 2 represents a linear or branched aliphatic hydrocarbon group having 8 to 22 carbon atoms which may have a hydroxyl group. N 2 represents the average degree of polymerization of glycerin, 1 to 10)
    The cosmetic composition according to claim 1, wherein the cosmetic composition is a compound having an HLB value of 9.0 to 15.0.
  5.  モノ若しくはポリグリセリン脂肪酸エステル(a2)を用いない場合、モノ若しくはポリグリセリンアルキル又はアルケニルエーテル(a1)、シリコーンオイル(b)、及び水(c)の化粧料用組成物全量に対する含有量が下記範囲である請求項1~3の何れかの項に記載の化粧料用組成物。
     モノ若しくはポリグリセリンアルキル又はアルケニルエーテル(a1):5.5重量%以上、9.0重量%未満
     シリコーンオイル(b):1.5重量%以上、5.0重量%未満
     水(c):86.0~93.0重量%
    When the mono- or polyglycerin fatty acid ester (a2) is not used, the content of the mono- or polyglycerin alkyl or alkenyl ether (a1), silicone oil (b), and water (c) with respect to the total amount of the cosmetic composition is in the following range. The cosmetic composition according to any one of claims 1 to 3, wherein
    Mono- or polyglycerin alkyl or alkenyl ether (a1): 5.5% by weight or more and less than 9.0% by weight Silicone oil (b): 1.5% by weight or more and less than 5.0% by weight Water (c): 86 0.0 to 93.0% by weight
  6.  モノ若しくはポリグリセリンアルキル又はアルケニルエーテル(a1)を用いない場合、モノ若しくはポリグリセリン脂肪酸エステル(a2)、シリコーンオイル、及び水の化粧料用組成物全量に対する含有量が下記範囲である請求項1又は4に記載の化粧料用組成物。
     モノ若しくはポリグリセリン脂肪酸エステル(a2):1.0~10.0重量%
     シリコーンオイル(b):1.0~10.0重量%
     水(c):80.0~98.0重量%
    When mono- or polyglycerin alkyl or alkenyl ether (a1) is not used, the content of mono- or polyglycerin fatty acid ester (a2), silicone oil, and water relative to the total amount of the cosmetic composition is in the following range: 4. The cosmetic composition according to 4.
    Mono or polyglycerol fatty acid ester (a2): 1.0 to 10.0% by weight
    Silicone oil (b): 1.0 to 10.0% by weight
    Water (c): 80.0 to 98.0% by weight
  7.  モノ若しくはポリグリセリンアルキル又はアルケニルエーテル(a1)及びモノ若しくはポリグリセリン脂肪酸エステル(a2)を用いる場合、モノ若しくはポリグリセリンアルキル又はアルケニルエーテル(a1)、モノ若しくはポリグリセリン脂肪酸エステル(a2)、シリコーンオイル、及び水の化粧料用組成物全量に対する含有量が下記範囲である請求項1~4の何れかの項に記載の化粧料用組成物。
     モノ若しくはポリグリセリンアルキル又はアルケニルエーテル(a1)及びモノ若しくはポリグリセリン脂肪酸エステル(a2):5.0重量%以上、10.0重量%未満
     シリコーンオイル(b):1.0重量%以上、6.0重量%未満
     水(c):80.0重量%以上
    When using mono or polyglycerol alkyl or alkenyl ether (a1) and mono or polyglycerol fatty acid ester (a2), mono or polyglycerol alkyl or alkenyl ether (a1), mono or polyglycerol fatty acid ester (a2), silicone oil, The cosmetic composition according to any one of claims 1 to 4, wherein the content of water and water relative to the total amount of the cosmetic composition is in the following range.
    Mono- or polyglycerin alkyl or alkenyl ether (a1) and mono- or polyglycerin fatty acid ester (a2): 5.0% by weight or more and less than 10.0% by weight Silicone oil (b): 1.0% by weight or more, 6. Less than 0% by weight Water (c): 80.0% by weight or more
PCT/JP2012/076832 2011-11-02 2012-10-17 Cosmetic composition WO2013065486A1 (en)

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JPS4829140B1 (en) * 1969-10-31 1973-09-07
JP2003267842A (en) * 2002-03-13 2003-09-25 Kao Corp Hair cosmetic
JP2005336089A (en) * 2004-05-26 2005-12-08 Kao Corp Multilayered cosmetic
JP2006347900A (en) * 2005-06-13 2006-12-28 Taiyo Kagaku Co Ltd Cleansing cosmetic
JP2007009167A (en) * 2005-05-30 2007-01-18 Riken Vitamin Co Ltd Surfactant composition and its manufacturing method, and detergent composition comprising the same
JP2007146029A (en) * 2005-11-29 2007-06-14 Lion Corp Detergent composition
JP2009227583A (en) * 2008-03-19 2009-10-08 Daicel Chem Ind Ltd Polyglycerol alkyl ether type nonionic surfactant
JP2010138113A (en) * 2008-12-11 2010-06-24 Kao Corp Skin preparation for external use
WO2011040256A1 (en) * 2009-09-30 2011-04-07 ダイセル化学工業株式会社 Gel-like composition
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JPS4829140B1 (en) * 1969-10-31 1973-09-07
JP2003267842A (en) * 2002-03-13 2003-09-25 Kao Corp Hair cosmetic
JP2005336089A (en) * 2004-05-26 2005-12-08 Kao Corp Multilayered cosmetic
JP2007009167A (en) * 2005-05-30 2007-01-18 Riken Vitamin Co Ltd Surfactant composition and its manufacturing method, and detergent composition comprising the same
JP2006347900A (en) * 2005-06-13 2006-12-28 Taiyo Kagaku Co Ltd Cleansing cosmetic
JP2007146029A (en) * 2005-11-29 2007-06-14 Lion Corp Detergent composition
JP2009227583A (en) * 2008-03-19 2009-10-08 Daicel Chem Ind Ltd Polyglycerol alkyl ether type nonionic surfactant
JP2010138113A (en) * 2008-12-11 2010-06-24 Kao Corp Skin preparation for external use
WO2011040256A1 (en) * 2009-09-30 2011-04-07 ダイセル化学工業株式会社 Gel-like composition
JP2011126805A (en) * 2009-12-16 2011-06-30 Mandom Corp Aqueous cleansing cosmetic

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