WO2024070386A1 - Hair treatment agent or head decoration product fiber treatment agent - Google Patents

Hair treatment agent or head decoration product fiber treatment agent Download PDF

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Publication number
WO2024070386A1
WO2024070386A1 PCT/JP2023/030870 JP2023030870W WO2024070386A1 WO 2024070386 A1 WO2024070386 A1 WO 2024070386A1 JP 2023030870 W JP2023030870 W JP 2023030870W WO 2024070386 A1 WO2024070386 A1 WO 2024070386A1
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Prior art keywords
treatment agent
mass
hair
component
less
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PCT/JP2023/030870
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French (fr)
Japanese (ja)
Inventor
早弥 古田
英輔 三好
崇 神田
優太 坂井
卓也 上原
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花王株式会社
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Publication of WO2024070386A1 publication Critical patent/WO2024070386A1/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
    • A61K8/34Alcohols
    • 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
    • A61K8/40Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing nitrogen
    • 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
    • A61K8/40Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing nitrogen
    • A61K8/41Amines
    • 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
    • A61K8/40Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing nitrogen
    • A61K8/42Amides
    • 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
    • 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
    • A61K8/896Polysiloxanes containing atoms other than silicon, carbon, oxygen and hydrogen, e.g. dimethicone copolyol phosphate
    • A61K8/898Polysiloxanes containing atoms other than silicon, carbon, oxygen and hydrogen, e.g. dimethicone copolyol phosphate containing nitrogen, e.g. amodimethicone, trimethyl silyl amodimethicone or dimethicone propyl PG-betaine
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q5/00Preparations for care of the hair
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q5/00Preparations for care of the hair
    • A61Q5/12Preparations containing hair conditioners

Definitions

  • the present invention relates to a hair treatment agent or a fiber treatment agent for head accessories such as wigs and extensions, and is preferably a rinse-off type hair cosmetic product such as a hair rinse, hair conditioner, hair treatment, or hair pack that is used after shampooing.
  • Hair cosmetics that are used after shampooing such as hair rinses and hair conditioners, contain cationic surfactants and higher alcohols as main ingredients and are intended to improve the condition of the hair surface by making the hair smooth and moisturized.
  • Patent Documents 1 to 3 disclose hair cosmetics that contain cationic surfactants, higher alcohols, silicones, etc. and give hair a pleasant feel.
  • Patent Document 1 discloses a hair cosmetic that combines a specific hydroxylamine, a quaternary ammonium salt, a higher alcohol, an amino group-containing silicone derivative selected from several options, and a methylpolysiloxane, giving hair a soft, moist finish without stickiness, and providing excellent finger-combability and softness when rinsing.
  • Patent Document 2 discloses a hair conditioning composition that combines two types of silicone that do not contain amino groups with a silicone that does contain amino groups, and mixes this with a gel matrix that contains a quaternary ammonium salt type cationic surfactant and a high melting point aliphatic compound, thereby providing improved conditioning effects such as a smooth feel and reduced friction.
  • Patent Document 3 discloses a hair cosmetic composition that contains a quaternary ammonium salt cationic surfactant, a higher alcohol, a phosphate group-containing silicone compound, and an amino-modified silicone compound, and that has good emulsion stability, is excellent in maintaining the smoothness and manageability of hair, and is not sticky.
  • Patent Document 1 Japanese Patent No. 5992257 (Patent Document 2) Japanese Patent Publication No. 2007-522226 (Patent Document 3) Japanese Patent Publication No. 2016-210686
  • the present invention provides a hair treatment agent or a fiber treatment agent for a head accessory product, which contains one or more components selected from the following components (A) to (C), as well as components (D) and (E), and the total content of components (D) and (E) is 1% by mass or more and 15% by mass or less.
  • A One or more cationic surfactants selected from the group consisting of ether amines or their salts, amido amines or their salts, and mono-long-chain alkyl quaternary ammonium salts having an alkyl group with 18 or more carbon atoms.
  • the present invention also provides a hair treatment method in which the above-mentioned hair treatment agent or fiber treatment agent for head accessories is applied to dyed hair or fibers for head accessories and then rinsed off with water.
  • Patent Documents 1 to 3 the hair cosmetics described in these documents are said to improve or sustain the feel and manageability of dry hair after finishing, and the hair cosmetic described in Patent Document 1 is said to be excellent in terms of runnability and softness when rinsing.
  • these conventional hair cosmetics were unable to maintain the smooth feel and lack of tangles in the wet state after repeated washing of treated hair.
  • the present invention relates to a hair treatment agent or a fiber treatment agent for head accessories that can maintain the lack of squeaky feeling and tangling in a wet state even after the treated hair or fiber for head accessories has been repeatedly washed.
  • the present invention also relates to a hair treatment agent or a fiber treatment agent for head accessories that has a good feel when used (non-sticky) and formulation stability.
  • the inventors have discovered that by using two specific cationic surfactants, a higher alcohol, and two specific silicones in a hair treatment agent or a fiber treatment agent for head accessories, preferably a hair cosmetic product such as a hair rinse or hair conditioner that is used after shampooing and is rinsed off, the treated hair or fiber for head accessories can be made to retain its smooth, tangle-free feel when wet. They have also discovered that the feel of use (non-stickiness) and formulation stability of the hair treatment agent or fiber treatment agent for head accessories are good.
  • the hair treatment agent or fiber treatment agent for head accessories of the present invention can maintain the absence of squeaky feeling or tangles in a wet state even after the treated hair or fiber for head accessories has been repeatedly washed, and the hair treatment agent or fiber treatment agent for head accessories also has excellent feel when used (non-sticky) and formulation stability.
  • the hair treatment agent of the present invention and the fiber treatment agent for head ornament products may be collectively referred to as the "treatment agent”.
  • hair primarily refers to hair on the head, and also includes hair used for head decoration products.
  • headwear product refers to, for example, hair wigs, hairpieces, weaving, hair extensions, braided hair, hair accessories, doll hair, and the like.
  • fiber for head accessories refers to a fiber used in the head accessories.
  • the treatment agent of the present invention is applied to hair or fibers for head accessories, and among these, hair is more preferred.
  • the fibers for head ornament products to which the treatment agent of the present invention is applied may be either naturally derived fibers or synthetic fibers, but naturally derived fibers are preferred.
  • Naturally derived fibers refer to fibers collected from natural animals and plants, or fibers artificially manufactured using polymers and oligomers such as proteins and polysaccharides derived from keratin, collagen, casein, soybeans, peanuts, corn, silk waste, silk protein (e.g., silk fibroin), etc. as raw materials.
  • fibers artificially manufactured using polymers and oligomers such as proteins and polysaccharides derived from animal hair, human hair, or proteins and polysaccharides derived from keratin, collagen, casein, soybeans, peanuts, corn, silk waste, silk protein (e.g., silk fibroin), etc. as raw materials are preferred, regenerated protein fibers derived from proteins derived from keratin, collagen, casein, soybean protein, peanut protein, corn protein, silk protein (e.g., silk fibroin), etc. as raw materials are more preferred, regenerated protein fibers such as regenerated collagen fibers derived from collagen as raw materials, regenerated silk fibers derived from silk fibroin as raw materials, etc.
  • polymers and oligomers such as proteins and polysaccharides derived from animal hair, human hair, or proteins and polysaccharides derived from keratin, collagen, casein, soybeans, peanuts, corn, silk waste, silk protein (e.g., silk fibroin), etc. as
  • Regenerated collagen fibers are even more preferred, and regenerated collagen fibers are even more preferred.
  • Regenerated collagen fibers can be produced by known techniques.
  • the composition of regenerated collagen fibers does not need to be 100% collagen, and may contain natural polymers, synthetic polymers, additives, etc. for quality improvement.
  • regenerated collagen fibers may be post-processed or post-treated.
  • the regenerated collagen fibers are preferably in the form of filaments. Filaments are generally taken out from bobbins or boxes. In addition, filaments coming out of the drying process in the manufacturing process of regenerated collagen fibers can also be used directly.
  • the synthetic fiber may be a fiber containing a synthetic resin as a main component.
  • the synthetic resin is preferably a thermoplastic resin, more preferably one or more selected from the group consisting of polyester resin, polyamide resin, polyimide resin, polyamideimide resin, vinyl chloride resin, polycarbonate resin, polyphenylene sulfide resin, and modacrylic resin (copolymer of acrylonitrile and vinyl chloride).
  • main component means a component whose content in the synthetic fiber is preferably 50% by mass or more, more preferably 60% by mass or more, even more preferably 70% by mass or more, even more preferably 80% by mass or more, and even more preferably 90% by mass or more, but not more than 100% by mass.
  • the synthetic fibers may further contain various components such as flame retardants, flame retardant assistants, light or heat stabilizers, fluorescent agents, antioxidants, antistatic agents, and ultraviolet absorbers, as long as the effects of the present invention are not impaired.
  • component (A) is preferably one or more selected from the group consisting of etheramines or salts thereof, and amidoamines or salts thereof, and more preferably a cationic surfactant containing an etheramine or a salt thereof.
  • the ether amine may be a compound represented by the following general formula (1).
  • R 1 represents a linear or branched alkyl or alkenyl group having 6 to 24 carbon atoms
  • R 2 and R 3 may be the same or different, and represent an alkyl group having 1 to 6 carbon atoms or -(A 1 O) m H
  • a 1 represents an alkylene group having 2 to 4 carbon atoms
  • m represents a number from 1 to 6
  • a 1 Os may be the same or different, and the arrangement is arbitrary
  • Y represents a hydrogen atom or a hydroxyl group.
  • etheramines or salts thereof include N,N-dimethyl-3-hexadecyloxypropylamine or salts thereof, N,N-dimethyl-3-octadecyloxypropylamine or salts thereof, hexadecyloxy(2-hydroxypropyl)dimethylamine or salts thereof, octadecyloxy(2-hydroxypropyl)dimethylamine or salts thereof, etc.
  • N,N-dimethyl-3-octadecyloxypropylamine or salts thereof, and octadecyloxy(2-hydroxypropyl)dimethylamine or salts thereof are more preferred.
  • amidoamine is a compound represented by the following general formula (2):
  • R 4 represents a linear or branched alkyl group having 17 to 21 carbon atoms
  • two R 5 represent the same alkyl group having 1 to 4 carbon atoms
  • n represents a number from 2 to 4.
  • amidoamines or their salts include dimethylaminoethyl stearate or its salts, dimethylaminopropyl stearate or its salts, diethylaminoethyl stearate or its salts, diethylaminopropyl stearate or its salts, dipropylaminoethyl stearate or its salts, dipropylaminopropyl stearate or its salts, dimethylaminopropyl stearate or its salts, dimethylaminopropyl stearate or its salts, diethyl ....
  • dimethylaminopropyl stearate or its salts diethylaminoethyl stearate or its salts, dimethylaminopropyl stearate or its salts, diethylaminopropyl stearate or its salts, dimethylaminopropyl stearate or its salts, diethylaminopropyl stearate or its salts, dimethylaminopropyl stearate or its salts, diethylaminopropyl stearate or its salts.
  • the salts of ether amines and amido amines include salts with organic or inorganic acids.
  • inorganic acids include salts with hydrochloric acid, sulfuric acid, phosphoric acid, and the like.
  • organic acids include salts with monocarboxylic acids such as acetic acid and propionic acid; salts with dicarboxylic acids such as malonic acid, succinic acid, glutaric acid, adipic acid, maleic acid, fumaric acid, and phthalic acid; salts with polycarboxylic acids such as polyglutamic acid; salts with hydroxycarboxylic acids such as glycolic acid, lactic acid, hydroxyacrylic acid, glyceric acid, malic acid, tartaric acid, and citric acid; and salts with acidic amino acids such as glutamic acid and aspartic acid.
  • salts with hydrochloric acid are more preferred as inorganic acid salts.
  • organic acid salts include salts with dicarboxylic acids, hydroxycarboxylic acids, and acidic amino acids.
  • salts with dicarboxylic acids include salts with maleic acid and succinic acid.
  • salts with hydroxycarboxylic acids include salts with glycolic acid, lactic acid, and malic acid.
  • salts with acidic amino acids include salts with glutamic acid.
  • Examples of mono-long chain alkyl quaternary ammonium salts with an alkyl group having 18 or more carbon atoms include compounds represented by the following general formula (3).
  • R 6 represents a saturated or unsaturated, linear or branched alkyl group having 18 to 22 carbon atoms
  • R 10 represents a saturated or unsaturated, linear or branched alkyl chain having 18 to 21 carbon atoms, and a represents an integer of 1 to 4
  • R 7 , R 8 and R 9 independently represent an alkyl group having 1 to 4 carbon atoms or a hydroxylalkyl group having 1 to 4 carbon atoms
  • X - represents a chloride ion, a bromide ion, a methosulfate ion or an ethosulfate ion.
  • Suitable examples of mono-long chain alkyl quaternary ammonium salts having an alkyl group with 18 or more carbon atoms include steartrimonium chloride, steartrimonium bromide, steartrimonium methosulfate, behentrimonium chloride, behentrimonium methosulfate, behenamidopropyltrimonium chloride, behenamidopropyltrimonium methosulfate, behenamidopropyl ethyldimonium ethosulfate, behenamidopropyl PG dimonium chloride, etc.
  • Component (A) may be used alone or in combination of two or more kinds.
  • the content of component (A) in the treatment agent of the present invention is preferably 1% by mass or more, more preferably 1.5% by mass or more, even more preferably 2% by mass or more, from the viewpoint of maintaining the absence of squeaky feeling and tangling in a wet state, improving the feeling of use of the treatment agent (non-stickiness) and the formulation stability of the treatment agent, and is preferably 10% by mass or less, more preferably 5% by mass or less, even more preferably 3% by mass or less, from the viewpoint of the feeling of use and stability of the treatment agent.
  • the specific range of the content of component (A) in the treatment agent of the present invention is preferably 1 to 10% by mass, more preferably 1.5 to 5% by mass, even more preferably 2 to 3% by mass.
  • Component (B) Mono-long chain alkyl quaternary ammonium salt having an alkyl group of 16 or less carbon atoms
  • the alkyl group of the mono long-chain alkyl quaternary ammonium salt of component (B) preferably has from 12 to 16 carbon atoms, more preferably from 14 to 16 carbon atoms, and even more preferably an alkyl group having 16 carbon atoms.
  • Specific examples of component (B) include cetrimonium chloride, cetrimonium bromide, cetrimonium methosulfate, etc., with cetrimonium chloride being preferred.
  • the content of component (B) in the treatment agent of the present invention is 0.1% by mass or more, preferably 0.2% by mass or more, and more preferably 0.3% by mass or more, from the viewpoint of maintaining the absence of squeaky feeling and tangling in a wet state. Also, the content of component (B) in the treatment agent of the present invention is 2.8% by mass or less, preferably 2.5% by mass or less, and more preferably 2.3% by mass or less, from the viewpoint of the stability of the treatment agent.
  • the specific range of the content of component (B) in the treatment agent of the present invention is 0.1 to 2.8% by mass, preferably 0.2 to 2.5% by mass or more, and more preferably 0.3 to 2.3% by mass.
  • the total content of components (A) and (B) in the treatment agent of the present invention is preferably 1.1% by mass or more, more preferably 1.7% by mass or more, even more preferably 2.3% by mass or more, from the viewpoint of maintaining the absence of squeaky feeling and tangling in a wet state and improving the feel of the treatment agent (non-stickiness) and the formulation stability, and is preferably 12.8% by mass or less, more preferably 7.5% by mass or less, even more preferably 5.3% by mass or less.
  • the specific range of the total content of components (A) and (B) in the treatment agent of the present invention is preferably 1.1 to 12.8% by mass, more preferably 1.7 to 7.5% by mass, even more preferably 2.3 to 5.3% by mass.
  • the mass ratio (B)/(A) of component (B) to component (A) is preferably 0.01 or more, more preferably 0.05 or more, even more preferably 0.1 or more, from the viewpoint of maintaining the absence of squeaky feeling and tangling in a wet state and improving the feeling of use of the treatment agent (non-stickiness) and the formulation stability, and is preferably 1.2 or less, more preferably 1.1 or less, even more preferably 1.0 or less, and even more preferably 0.5 or less.
  • the specific range of the mass ratio (B)/(A) of component (B) to component (A) is preferably 0.01 to 1.2, more preferably 0.05 to 1.1, even more preferably 0.1 to 1.0, and even more preferably 0.1 to 0.5.
  • the mass ratio (B)/(A) is preferably in the range of 0.1 to 0.17.
  • the higher alcohol of component (C) may be either a linear or branched, saturated or unsaturated aliphatic alcohol, preferably a linear or branched saturated aliphatic alcohol, more preferably a linear saturated aliphatic alcohol.
  • the number of carbon atoms of the higher alcohol of component (C) is preferably 12 or more, more preferably 14 or more, even more preferably 16 or more, and is preferably 22 or less, more preferably 20 or less, even more preferably 18 or less.
  • the specific range of the number of carbon atoms of the higher alcohol of component (C) is preferably 12 to 22, more preferably 14 to 20, even more preferably 16 to 18.
  • component (C) examples include lauryl alcohol, myristyl alcohol, cetyl alcohol, stearyl alcohol, arachyl alcohol, hexyldecanol, isostearyl alcohol, oleyl alcohol, and 2-octyldodecanol.
  • stearyl alcohol, cetyl alcohol, and myristyl alcohol are preferred, stearyl alcohol and cetyl alcohol are more preferred, and stearyl alcohol is even more preferred.
  • These components (C) can be used alone or in combination of two or more.
  • the content of component (C) in the treatment agent of the present invention is 1% by mass or more, preferably 3% by mass or more, and more preferably 5% by mass or more, from the viewpoint of the stability of the treatment agent. Also, the content of component (C) in the treatment agent of the present invention is 15% by mass or less, preferably 12% by mass or less, and more preferably 10% by mass or less, from the viewpoint of smoothness from application to rinsing and after drying.
  • the specific range of the content of component (C) in the treatment agent of the present invention is 1 to 15% by mass, preferably 3 to 12% by mass, and more preferably 5 to 10% by mass or more.
  • Component (D) One or more modified silicones selected from the group consisting of amino-modified silicones and aminopolyether-modified silicones]
  • the amino-modified silicone will also be referred to as “component (D1)”
  • the amino polyether-modified silicone will also be referred to as “component (D2).”
  • the amino-modified silicone refers to a silicone that has an amino group and does not have a polyether structure.
  • An example of the component (D1) is an amino-modified silicone represented by the following general formula (4).
  • R 10 each independently represents a methyl group or a hydroxy group
  • R 11 each independently represents an alkyl group having 1 to 30 carbon atoms, a hydroxy group, or R 12.
  • R 12 represents a monovalent group represented by -R 13 -Z 1 (R 13 represents a single bond or a divalent hydrocarbon group having 1 to 20 carbon atoms, and Z 1 represents a primary to tertiary amino group-containing group or an ammonium group-containing group).
  • a represents a number of 0 to 3,000
  • b represents a number of 1 to 3,000.
  • R 10 is preferably a methyl group
  • R 11 is preferably a methyl group or R 12 .
  • R13 is preferably a divalent hydrocarbon group having 1 to 20 carbon atoms, more preferably a divalent saturated hydrocarbon group having 1 to 20 carbon atoms, even more preferably a linear or branched divalent saturated hydrocarbon group having 1 to 6 carbon atoms, still more preferably a methylene group, ethylene group, trimethylene group, propylene group, tetramethylene group, or hexamethylene group, and even more preferably a trimethylene group or propylene group.
  • Z 1 is preferably an amino group-containing group represented by -N(R 14 ) 2 , -NR 14 (CH 2 ) c N(R 15 ) 2 , or -NR 14 (CH 2 ) c N(R 15 )CO-R 16.
  • R 14 and R 15 each independently represent a hydrogen atom or an alkyl group having 1 to 3 carbon atoms, preferably a hydrogen atom or a methyl group.
  • R 16 represents an alkyl group having 1 to 3 carbon atoms.
  • c represents a number of 1 to 6, preferably a number of 2 to 4.
  • R 12 is preferably --(CH 2 ) 3 --NH 2 , --(CH 2 ) 3 --N(CH 3 ) 2 , --(CH 2 ) 3 --NH--(CH 2 ) 2 --NH 2 , or --(CH 2 ) 2 --NH--(CH 2 ) 2 --N(CH 3 ) 2 , and more preferably --(CH 2 ) 3 --NH 2 or --(CH 2 ) 3 --NH--(CH 2 ) 2 --NH 2 .
  • the amino-modified silicone represented by general formula (4) is preferably one or more selected from the group consisting of amodimethicone, aminopropyl dimethicone, bis(aminopropyl) dimethicone, and bis(cetearyl) amodimethicone, and more preferably a compound represented by any of the following general formulas (4a) to (4d).
  • Component (D1) may be used alone or in combination of two or more. From the viewpoint of smoothness from application to rinsing and after drying, component (D1) is more preferably an amino-modified silicone (amodimethicone) represented by the above general formula (4a).
  • the kinetic viscosity of component (D1) at 25°C is preferably at least 20 mm 2 /s, more preferably at least 100 mm 2 /s, even more preferably at least 500 mm 2 /s, and is preferably at most 10,000 mm 2 /s, more preferably at most 5,000 mm 2 /s, even more preferably at most 2,000 mm 2 /s.
  • the specific range of the kinetic viscosity of component (D1) at 25°C is preferably 20 to 10,000 mm 2 /s, more preferably 100 to 5,000 mm 2 /s, even more preferably 500 to 2,000 mm 2 /s.
  • the kinetic viscosity of component (D1) is a value measured at 25°C in accordance with the "Method for measuring viscosity of liquids" specified in JIS Z8803:2011 or ASTM D 445-46T, and can be measured, for example, using an Ubbelohde viscometer.
  • amino-modified silicones can also be used as component (D1).
  • an amino-modified silicone (amodimethicone) represented by general formula (4a) is "Silicone SF 8457 C” manufactured by Dow-Toray.
  • aminopolyether-modified silicone means a silicone having an amino group and a polyether structure.
  • the polyether structure in component (D2) is preferably a polyoxyalkylene group from the viewpoint of smoothness from application through rinsing and after drying.
  • the ratio Si/AO is preferably 0.05 or more, more preferably 0.1 or more, even more preferably 0.3 or more, still more preferably 0.5 or more, still more preferably 0.7 or more, and is preferably 3.0 or less, more preferably 2.8 or less, still more preferably 2.6 or less, and still more preferably 2.4 or less.
  • the specific range of the ratio Si/AO in component (D2) is preferably 0.05 to 3.0, more preferably 0.1 to 2.8, even more preferably 0.3 to 2.8, still more preferably 0.5 to 2.6, and still more preferably 0.7 to 2.4.
  • the Si/AO ratio can be calculated from the integral value of hydrogen atoms bonded to silicon and H of hydrocarbon groups, and the integral value of H of oxyalkylene groups, measured by 1 H-NMR measurement.
  • the nitrogen content of component (D2) is preferably 0.1% by mass or more, more preferably 0.2% by mass or more, even more preferably 0.5% by mass or more, still more preferably 1.0% by mass or more, and preferably 2.5% by mass or less, more preferably 2.0% by mass or less, even more preferably 1.8% by mass or less, and even more preferably 1.5% by mass or less.
  • the specific range of the nitrogen content of component (D2) is preferably 0.1 to 2.5% by mass, more preferably 0.2 to 2.0% by mass, even more preferably 0.5 to 1.8% by mass, and even more preferably 1.0 to 1.5% by mass.
  • the nitrogen content of component (D2) is a value measured in accordance with the potentiometric titration method specified in JIS K0113:2005.
  • Component (D2) is preferably an aminopolyether-modified silicone represented by the following general formula (5):
  • R 17 represents a hydrogen atom or a monovalent hydrocarbon group having 1 to 6 carbon atoms.
  • R 18 represents R 17 or E.
  • E represents a monovalent group represented by -R 19 -Z 2 (R 19 represents a single bond or a divalent hydrocarbon group having 1 to 20 carbon atoms, and Z 2 represents a primary to tertiary amino group-containing group or an ammonium group-containing group).
  • W represents a divalent saturated hydrocarbon group having 1 to 6 carbon atoms.
  • d is a number of 2 or more
  • e is a number of 1 or more
  • f is a number of 2 or more and 100 or less
  • g is a number of 1 or more.
  • x is a number of 2 or more and 10 or less.
  • the structural units in the parentheses may be bonded in any order, and may be bonded in a block or random form.
  • f C x H 2x O may be the same or different.
  • multiple R 17 , R 18 , E, and W may be the same or different.
  • component (D2) is an aminopolyether-modified silicone represented by general formula (5)
  • the Si/AO is represented by (d+e+1)/f.
  • R 17 is preferably a hydrogen atom, an alkyl group having 1 to 6 carbon atoms, or a phenyl group, more preferably a methyl group or an ethyl group, and even more preferably a methyl group.
  • R 19 is preferably a divalent hydrocarbon group having 1 to 20 carbon atoms, more preferably a divalent saturated hydrocarbon group having 1 to 20 carbon atoms, even more preferably a linear or branched divalent saturated hydrocarbon group having 1 to 6 carbon atoms, still more preferably a methylene group, ethylene group, trimethylene group, propylene group, tetramethylene group, or hexamethylene group, and even more preferably a trimethylene group or propylene group.
  • Z 2 is preferably an amino group-containing group represented by -N(R 20 ) 2 , -NR 20 (CH 2 ) h N(R 20 ) 2 , or -NR 20 (CH 2 ) h N(R 21 )CO-R 22.
  • R 20 and R 21 each independently represent a hydrogen atom or an alkyl group having 1 to 3 carbon atoms, and are preferably a hydrogen atom or a methyl group.
  • R 22 represents an alkyl group having 1 to 3 carbon atoms.
  • h represents a number of 1 to 6, and is preferably a number of 2 to 4.
  • preferred E groups are -( CH2 ) 3 - NH2 , -( CH2 ) 3 -N( CH3 ) 2 , -( CH2 ) 3 -NH-( CH2 ) 2 -NH2, or -( CH2 ) 2 -NH-( CH2 ) 2 -N( CH3 ) 2 , and more preferably -( CH2 ) 3 -NH-( CH2 ) 2 - NH2 .
  • W is preferably an ethylene group, a propylene group, a trimethylene group, an n-butylene group (a tetramethylene group) or an i-butylene group, and more preferably an n-butylene group or an i - butylene group.
  • the i- butylene group referred to here includes --CH( CH3 ) CH2CH2-- , --CH2CH ( CH3 ) CH2-- , and --CH2CH2CH ( CH3 )--.
  • d is preferably a number between 2 and 1000, more preferably between 2 and 100.
  • e is preferably a number between 1 and 50, f is preferably a number between 4 and 50, more preferably between 10 and 18, and
  • g is preferably a number between 1 and 100.
  • x is preferably a number from 2 to 6, more preferably from 2 to 4.
  • Component (D2) is more preferably an aminopolyether-modified silicone represented by the following general formula (5a):
  • the kinetic viscosity of component (D2) at 25°C is preferably at least 5,000 mm 2 /s, more preferably at least 20,000 mm 2 /s, even more preferably at least 40,000 mm 2 /s, and is preferably at most 200,000 mm 2 /s, more preferably at most 150,000 mm 2 /s, even more preferably at most 100,000 mm 2 /s.
  • the specific range of the kinetic viscosity of component (D2) at 25°C is preferably 5,000 to 200,000 mm 2 /s, more preferably 20,000 to 150,000 mm 2 /s, even more preferably 40,000 to 100,000 mm 2 /s.
  • the kinematic viscosity of component (D2) can be measured in the same manner as for component (D1).
  • aminopolyether-modified silicones can also be used as component (D2).
  • Component (D) may be used alone or in combination of two or more types.
  • component (D) is preferably one or more selected from the group consisting of the amino-modified silicone represented by general formula (4) and the amino polyether-modified silicone represented by general formula (5), more preferably one or more selected from the group consisting of the amino-modified silicone represented by general formula (4a) and the amino polyether-modified silicone represented by general formula (5a), and even more preferably the amino-modified silicone represented by general formula (4a).
  • the content of component (D) in the treatment agent of the present invention is preferably 0.1% by mass or more, more preferably 0.4% by mass or more, even more preferably 0.8% by mass or more, and is preferably 10% by mass or less, more preferably 7% by mass or less, even more preferably 5% by mass or less, from the viewpoint of improving smoothness from application to rinsing and after drying, and maintaining the lack of squeaky feeling and tangling in a wet state.
  • the specific range of the content of component (D) in the treatment agent of the present invention is preferably 0.1 to 10% by mass, more preferably 0.4 to 7% by mass, even more preferably 0.8 to 5% by mass.
  • the dimethicone component (E) is preferably low volatility, and from this viewpoint, the kinematic viscosity at 25°C is preferably 500 mm2/s or more, more preferably 1,000 mm2 /s or more, even more preferably 5,000 mm2/s or more, even more preferably 10,000 mm2 /s or more, even more preferably 30,000 mm2 /s or more, even more preferably 50,000 mm2 /s or more, and preferably 1,000,000 mm2 /s or less, more preferably 50,000 mm2 /s or less, even more preferably 300,000 mm2 /s or less, and even more preferably 200,000 mm2 /s or less.
  • the kinetic viscosity of dimethicone in component (E) at 25°C is preferably 500 to 1,000,000 mm2 /s, more preferably 1,000 to 500,000 mm2 /s, even more preferably 5,000 to 300,000 mm2 /s, still more preferably 10,000 to 200,000 mm2 /s, still more preferably 30,000 to 200,000 mm2 /s, and even more preferably 50,000 to 200,000 mm2 /s.
  • the viscosity is taken as the viscosity of the mixture.
  • the kinetic viscosity of component (E) is a value measured at 25°C according to the "Method for measuring viscosity of liquids" specified in JIS Z8803:2011 or in accordance with ASTM D 445-46T, and can be measured, for example, using an Ubbelohde viscometer.
  • dimethicone examples include Silicone KHS-3 (dynamic viscosity 100,000 to 150,000 mm2 /s (25°C)) and Silicone KHS-9 (dynamic viscosity 5,000 to 25,000 mm2 /s (25°C)) (both manufactured by Shin-Etsu Chemical Co., Ltd.).
  • the content of component (E) in the treatment agent of the present invention is preferably 0.1% by mass or more, more preferably 1% by mass or more, even more preferably 2% by mass or more, and is preferably 10% by mass or less, more preferably 8% by mass or less, even more preferably 6% by mass or less, from the viewpoint of improving smoothness from application to rinsing and after drying, and maintaining a lack of squeaky feeling and tangling in a wet state.
  • the specific range of the content of component (E) in the treatment agent of the present invention is preferably 0.1 to 10% by mass, more preferably 1 to 8% by mass, even more preferably 2 to 6% by mass.
  • the treatment agent of the present invention may contain at least one of components (D) and (E), but it is preferable to contain both components (D) and (E).
  • the total content of components (D) and (E) is 1% by mass or more, preferably 2% by mass or more, more preferably 3% by mass or more, even more preferably 5% by mass or more, and 15% by mass or less, preferably 12% by mass or less, more preferably 10% by mass or less, even more preferably 8% by mass or less, from the viewpoint of improving smoothness from application to rinsing and after drying, and maintaining the lack of squeaky feeling and tangling in a wet state.
  • the specific range of the total content of components (D) and (E) is 1 to 15% by mass, preferably 1 to 12% by mass, more preferably 1 to 10% by mass, even more preferably 2 to 10% by mass, even more preferably 3 to 10% by mass, even more preferably 5 to 8% by mass or more.
  • the mass ratio (E)/(D) of component (E) to component (D) is preferably 0.1 or more, more preferably 1 or more, even more preferably 2 or more, and even more preferably 3.5 or more, and is preferably 15 or less, more preferably 10 or less, and even more preferably 7 or less, from the viewpoint of improving smoothness from application to rinsing and after drying, and maintaining the lack of squeaky feeling and tangling in a wet state.
  • the specific range of the mass ratio (E)/(D) of component (E) to component (D) is preferably 0.1 to 15, more preferably 1 to 10, even more preferably 2 to 7, and even more preferably 3.5 to 7.
  • the treatment agent of the present invention preferably further contains an organic acid or a salt thereof.
  • the organic acid or the salt thereof functions as an internal modifying component for hair or fibers for head accessories, and can provide smoother combing properties.
  • the organic acid includes carboxylic acid compounds, preferably compounds having a molecular weight of 500 or less, more preferably 200 or less.
  • Carboxylic acid compounds include, for example, aliphatic monocarboxylic acids having 4 or less carbon atoms, such as acetic acid, propionic acid, butanoic acid, etc.; aromatic monocarboxylic acids, such as benzoic acid; aliphatic dicarboxylic acids, such as malonic acid, succinic acid, glutaric acid, adipic acid, maleic acid, fumaric acid, etc.; aromatic dicarboxylic acids, such as phthalic acid, isophthalic acid, etc.; polycarboxylic acids, such as polyglutamic acid; hydroxycarboxylic acids, such as lactic acid, malic acid, glycolic acid, hydroxyacrylic acid, glyceric acid, tartaric acid, citric acid, etc.; acidic amino acids, such as glutamic acid, aspartic acid, etc. Any of these can be used alone or in combination of two or more.
  • succinic acid lactic acid, malic acid and glycolic acid
  • succinic acid lactic acid
  • malic acid and lactic acid it is preferably one or more selected from the group consisting of succinic acid, lactic acid, malic acid and glycolic acid, more preferably one or more selected from the group consisting of succinic acid, malic acid and lactic acid, and even more preferably one or more selected from malic acid and lactic acid.
  • the organic acid may be at least partially in the form of an organic acid salt when blended.
  • an alkali metal salt or alkaline metal salt of the organic acid is preferred, an alkali metal salt is more preferred, one or more selected from the group consisting of sodium salts and potassium salts is even more preferred, and a sodium salt is even more preferred.
  • the proportion of organic acid salts in the total amount of organic acids and organic acid salts is preferably 50% by mass or less, more preferably 20% by mass or less, and even more preferably 5% by mass or less, and may be 0% by mass.
  • the proportion of organic acid salts referred to here is calculated by converting the amount of organic acid salts into the amount of organic acid.
  • the content of the organic acid in the treatment agent of the present invention is preferably 0.1% by mass or more, more preferably 0.5% by mass or more, even more preferably 1% by mass or more, and preferably 5% by mass or less, more preferably 3% by mass or less, even more preferably 2% by mass or less.
  • the specific range of the content of the organic acid in the treatment agent of the present invention is preferably 0.1 to 5% by mass, more preferably 0.5 to 3% by mass, even more preferably 1 to 2% by mass.
  • the treatment agent of the present invention preferably further contains an aromatic alcohol.
  • the aromatic alcohol is used from the viewpoint of promoting the penetration of the organic acid, which functions as an internal modifying component of the hair or the fiber for head ornament products, into the inside of the hair or the fiber for head ornament products, and examples thereof include benzyl alcohol, phenoxyethanol, and 2-benzyloxyethanol. Any of these may be used alone or in combination of two or more kinds.
  • the content of aromatic alcohol in the treatment agent of the present invention is preferably 0.01% by mass or more, more preferably 0.05% by mass or more, even more preferably 0.1% by mass or more, from the viewpoint of promoting the penetration of organic acid into the interior of hair or fibers for head accessories, and is preferably 2% by mass or less, more preferably 1% by mass or less, even more preferably 0.5% by mass or less.
  • the specific range of the content of aromatic alcohol in the treatment agent of the present invention is preferably 0.01 to 2% by mass, more preferably 0.05 to 1% by mass, even more preferably 0.1 to 0.5% by mass.
  • the treatment agent of the present invention may contain an appropriate cationic surfactant other than components (A) and (B) from the viewpoints of imparting a suitable viscosity as a hair treatment agent or a fiber treatment agent for head ornament products and improving the feeling of use.
  • the content of the cationic surfactant other than components (A) and (B) in the treatment agent is preferably 1% by mass or less, more preferably 0.5% by mass or less, even more preferably 0.1% by mass or less, and even more preferably the treatment agent is substantially free of cationic surfactants other than components (A) and (B).
  • the treatment agent of the present invention contains the cationic surfactants of components (A) and (B), if an excessive amount of anionic surfactant is added, the cationic surfactant and the anionic surfactant may form aggregates. Therefore, the content of the anionic surfactant in the treatment agent is preferably 0.5 mass% or less, more preferably 0.1 mass% or less, even more preferably 0.05 mass% or less, and even more preferably substantially free of anionic surfactant.
  • the treatment agent of the present invention contains water as a medium.
  • the water constitutes the balance of components (A) to (E) and other components.
  • the treatment agent of the present invention may further contain other components generally used in hair cosmetics or fiber treatment agents for head accessories, depending on the purpose.
  • silicones other than components (D) and (E) such as cyclic silicone, dimethiconol, polyether-modified silicone, polyglycidol-modified silicone, methylphenylpolysiloxane, fatty acid-modified silicone, alcohol-modified silicone, alkoxy-modified silicone, epoxy-modified silicone, fluorine-modified silicone, and alkyl-modified silicone; polymeric compounds, such as cationic cellulose, hydroxyalkyl cellulose, and highly polymerized polyethylene oxide; polyoxyethylene alkyl ether, polyoxyethylene sorbitan fatty acid ester, glycerin mono fatty acid ester, polyglycerin fatty acid ester, polyoxyethylene hydrogenated castor oil, and sucrose.
  • Nonionic surfactants such as fatty acid esters, polyglycerol alkyl ethers, fatty acid alkanolamides, and alkyl glycosides; hydrocarbons such as squalene, squalane, liquid paraffin, liquid isoparaffin, and cycloparaffin; glycerides such as castor oil, cocoa oil, mink oil, avocado oil, and olive oil; waxes such as beeswax, spermaceti, lanolin, and carnauba wax; esters such as isopropyl palmitate, isopropyl myristate, octyldodecyl myristate, hexyl laurate, cetyl lactate, propylene glycol monostearate, oleyl oleate, hexadecyl 2-ethylhexanoate, isononyl isononanoate, and tridecyl isononanoate.
  • oils such as isostearyl glyceryl ether and polyoxypropylene butyl ether; alcohols such as ethanol, 1-propanol, 2-propanol, butanol, ethylene glycol, propylene glycol, methyl carbitol, ethyl carbitol, propyl carbitol, butyl carbitol, triethylene glycol monoethyl ether, triethylene glycol monobutyl ether, and glycerin; antibacterial agents such as zinc pyrithione and benzalkonium chloride.
  • oils such as isostearyl glyceryl ether and polyoxypropylene butyl ether
  • alcohols such as ethanol, 1-propanol, 2-propanol, butanol, ethylene glycol, propylene glycol, methyl carbitol, ethyl carbitol, propyl carbitol, butyl carbitol, triethylene glycol monoethyl ether
  • ingredients that may be used include dandruff agents; pH adjusters; vitamins; disinfectants; anti-inflammatory agents; preservatives; chelating agents; moisturizers such as panthenol; colorants such as dyes and pigments; extracts such as polar solvent extracts of eucalyptus, proteins or hydrolysates thereof obtained from shells or pearls having nacre, proteins or hydrolysates thereof obtained from silk, protein-containing extracts obtained from the seeds of legumes, ginseng extract, rice germ extract, hibamata extract, camellia extract, aloe extract, shell ginger leaf extract, and chlorella extract; pearl powders such as titanium mica; cooling agents such as menthol; fragrances; pigments; ultraviolet absorbers; antioxidants; and other ingredients listed in the Encyclopedia of Shampoo Ingredients (MICELLE PRESS).
  • dandruff agents pH adjusters
  • vitamins disinfectants
  • anti-inflammatory agents such as panthenol
  • colorants such as dyes and pigments
  • extracts such as polar solvent extracts of
  • the pH of the treatment agent of the present invention is preferably 2.0 or more, more preferably 2.5 or more, and is preferably 7.5 or less, more preferably 6.5 or less, and even more preferably 5.5 or less.
  • the specific range of the pH of the treatment agent of the present invention is preferably 2.0 to 7.5, more preferably 2.5 to 6.5, and even more preferably 2.5 to 5.5.
  • the pH of the treatment agent refers to the value at 25°C when diluted 20 times by mass with water. The above pH can be measured using a pH meter.
  • the viscosity of the treatment agent of the present invention is preferably in the range of 500 mPa ⁇ s to 100,000 mPa ⁇ s from the viewpoint of maintaining the absence of squeaky feeling and tangling in a wet state. From the viewpoint of applicability to hair or fibers for head ornament products and prevention of dripping from hands, hair, or fibers for head ornament products, it is preferably 1,000 mPa ⁇ s or more, more preferably 5,000 mPa ⁇ s or more, and even more preferably 10,000 mPa ⁇ s or more.
  • the viscosity of the treatment agent of the present invention is preferably 50,000 mPa ⁇ s or less, more preferably 40,000 mPa ⁇ s or less, and even more preferably 30,000 mPa ⁇ s or less.
  • the specific range of the viscosity of the treatment agent of the present invention is preferably 500 to 100,000 mPa ⁇ s, more preferably 1,000 to 50,000 mPa ⁇ s, even more preferably 5,000 to 40,000 mPa ⁇ s, and even more preferably 10,000 to 30,000 mPa ⁇ s.
  • the viscosity is measured at 30° C. using a Brookfield viscometer or a BM type viscometer.
  • the rotor and rotation speed used during measurement are selected according to the viscosity of the treatment agent, and appropriate conditions are selected in accordance with the manual or the like.
  • the treatment agent of the present invention can be suitably used as an in-bath agent (a type that is applied to hair or fibers for head ornament products and then washed off) such as a pre-shampoo treatment, shampoo, hair rinse, hair conditioner, hair treatment, hair pack, or after-shampoo treatment; or an out-bath agent (a type that is applied to hair or fibers for head ornament products and then not washed off) such as a non-aerosol foam, aerosol foam, hair gel, hair mousse, hair mist, hair lotion, hair oil, or styling agent.
  • an in-bath agent a type that is applied to hair or fibers for head ornament products and then washed off
  • an out-bath agent a type that is applied to hair or fibers for head ornament products and then not washed off
  • an in-bath agent (a type that is applied to hair or fibers for head ornament products and then washed off) is preferred.
  • the hair or fibers for head ornament products to be treated is not particularly limited, but the agent can be suitably used for hair or fibers for head ornament products after dyeing treatment such as hair coloring.
  • conditioning of hair or fibers for head accessories can be performed by applying the treatment agent of the present invention to the hair or fibers for head accessories and then rinsing it off with water. This allows the treated hair or fibers for head accessories to maintain their lack of squeaky feeling and tangles in a wet state even after repeated washing.
  • a hair treatment agent or a fiber treatment agent for a head accessory product comprising one or more components selected from the following components (A) to (C), as well as components (D) and (E), wherein the total content of components (D) and (E) is 1% by mass or more and 15% by mass or less.
  • a cationic surfactants selected from the group consisting of ether amines or their salts, amido amines or their salts, and mono-long-chain alkyl quaternary ammonium salts having an alkyl group with 18 or more carbon atoms.
  • etheramine is preferably a compound represented by the following general formula (1):
  • R 1 represents a linear or branched alkyl or alkenyl group having 6 to 24 carbon atoms
  • R 2 and R 3 may be the same or different, and represent an alkyl group having 1 to 6 carbon atoms or -(A 1 O) m H
  • a 1 represents an alkylene group having 2 to 4 carbon atoms
  • m represents a number from 1 to 6
  • a 1 Os may be the same or different, and the arrangement is arbitrary
  • Y represents a hydrogen atom or a hydroxyl group.
  • etheramine or its salt is preferably one or more selected from N,N-dimethyl-3-hexadecyloxypropylamine or its salt, N,N-dimethyl-3-octadecyloxypropylamine or its salt, hexadecyloxy(2-hydroxypropyl)dimethylamine or its salt, and octadecyloxy(2-hydroxypropyl)dimethylamine or its salt, more preferably one or more selected from N,N-dimethyl-3-octadecyloxypropylamine or its salt, and octadecyloxy(2-hydroxypropyl)dimethylamine or its salt.
  • a hair treatment agent or a fiber treatment agent for head accessories according to any one of ⁇ 1> to ⁇ 3>, wherein the amidoamine is preferably a compound represented by the following general formula (2):
  • R 4 represents a linear or branched alkyl group having 17 to 21 carbon atoms
  • two R 5 represent the same alkyl group having 1 to 4 carbon atoms
  • n represents a number from 2 to 4.
  • the amidoamine or its salt is preferably one or more selected from dimethylaminoethylamide stearate or its salt, dimethylaminopropylamide stearate or its salt, diethylaminoethylamide stearate or its salt, diethylaminopropylamide stearate or its salt, dipropylaminoethylamide stearate or its salt, dipropylaminopropylamide stearate or its salt, dimethylaminopropylamide behenate or its salt, and diethylaminopropylamide behenate or its salt, more preferably one or more selected from dimethylaminopropylamide stearate or its salt, diethylaminoethylamide stearate or its salt, dimethylaminopropylamide behenate or its salt, and diethylaminopropylamide behenate or its salt, more preferably one or more selected from dimethylaminopropylamide
  • a hair treatment agent or a fiber treatment agent for head accessories according to any one of ⁇ 1> to ⁇ 5>, wherein the mono-long-chain alkyl quaternary ammonium salt having an alkyl group having 18 or more carbon atoms is preferably a compound represented by the following general formula (3):
  • R 6 represents a saturated or unsaturated, linear or branched alkyl group having 18 to 22 carbon atoms
  • R 10 represents a saturated or unsaturated, linear or branched alkyl chain having 18 to 21 carbon atoms, and a represents an integer of 1 to 4
  • R 7 , R 8 and R 9 independently represent an alkyl group having 1 to 4 carbon atoms or a hydroxylalkyl group having 1 to 4 carbon atoms
  • X - represents a chloride ion, a bromide ion, a methosulfate ion or an ethosulfate ion.
  • a hair treatment agent or a fiber treatment agent for head accessories according to any one of ⁇ 1> to ⁇ 6>, wherein the mono long-chain alkyl quaternary ammonium salt having an alkyl group having 18 or more carbon atoms is preferably one or more selected from steartrimonium chloride, steartrimonium bromide, steartrimonium methosulfate, behentrimonium chloride, behentrimonium methosulfate, behenamidopropyltrimonium chloride, behenamidopropyltrimonium methosulfate, behenamidopropyl ethyldimonium ethosulfate, and behenamidopropyl PG-dimonium chloride.
  • a hair treatment agent or a fiber treatment agent for head accessories according to any one of ⁇ 1> to ⁇ 7>, in which the content of component (A) is preferably 1 to 10 mass%, more preferably 1.5 to 5 mass%, and even more preferably 2 to 3 mass%.
  • the hair treatment agent or fiber treatment agent for head accessories according to any one of ⁇ 1> to ⁇ 8>, wherein the alkyl group of the mono-long-chain alkyl quaternary ammonium salt of component (B) preferably has 12 to 16 carbon atoms, more preferably has 14 to 16 carbon atoms, and even more preferably has 16 carbon atoms.
  • component (B) is preferably one or more selected from cetrimonium chloride, cetrimonium bromide, and cetrimonium methosulfate, more preferably cetrimonium chloride.
  • a hair treatment agent or a fiber treatment agent for head accessories according to any one of ⁇ 1> to ⁇ 10>, wherein the content of component (B) is preferably 0.2 to 2.5 mass% or more, more preferably 0.3 to 2.3 mass%.
  • a hair treatment agent or a fiber treatment agent for head accessories according to any one of ⁇ 1> to ⁇ 11>, wherein the total content of components (A) and (B) is preferably 1.1 to 12.8% by mass, more preferably 1.7 to 7.5% by mass, and even more preferably 2.3 to 5.3% by mass.
  • the hair treatment agent or fiber treatment agent for head accessories according to any one of ⁇ 1> to ⁇ 12>, wherein the mass ratio (B)/(A) of component (B) to component (A) is preferably 0.01 to 1.2, more preferably 0.05 to 1.1, even more preferably 0.1 to 1.0, and even more preferably 0.1 to 0.5.
  • ⁇ 14> The hair treatment agent or fiber treatment agent for head accessories according to any one of ⁇ 1> to ⁇ 13>, wherein the carbon number of the higher alcohol of component (C) is preferably 12 to 22, more preferably 14 to 20, and even more preferably 16 to 18.
  • component (C) is preferably at least one selected from lauryl alcohol, myristyl alcohol, cetyl alcohol, stearyl alcohol, arachyl alcohol, hexyldecanol, isostearyl alcohol, oleyl alcohol, and 2-octyldodecanol, more preferably at least one selected from stearyl alcohol, cetyl alcohol, and myristyl alcohol, more preferably at least one selected from stearyl alcohol and cetyl alcohol, and even more preferably stearyl alcohol.
  • a hair treatment agent or a fiber treatment agent for head accessories according to any one of ⁇ 1> to ⁇ 15>, in which the content of component (C) is preferably 3 to 12 mass%, more preferably 5 to 10 mass% or more.
  • a hair treatment agent or a fiber treatment agent for head accessories according to any one of ⁇ 1> to ⁇ 16>, wherein the amino-modified silicone of component (D) is preferably represented by the following general formula (4):
  • R 10 each independently represents a methyl group or a hydroxy group
  • R 11 each independently represents an alkyl group having 1 to 30 carbon atoms, a hydroxy group, or R 12.
  • R 12 represents a monovalent group represented by -R 13 -Z 1 (R 13 represents a single bond or a divalent hydrocarbon group having 1 to 20 carbon atoms, and Z 1 represents a primary to tertiary amino group-containing group or an ammonium group-containing group).
  • a represents a number of 0 to 3,000
  • b represents a number of 1 to 3,000.
  • the amino-modified silicone represented by the general formula (4) is preferably one or more selected from the group consisting of amodimethicone, aminopropyl dimethicone, bis(aminopropyl) dimethicone, and bis(cetearyl) amodimethicone, more preferably a compound represented by any one of the following general formulas (4a) to (4d), and even more preferably an amino-modified silicone (amodimethicone) represented by the following general formula (4a).
  • the hair treatment agent or fiber treatment agent for head ornament products according to any one of ⁇ 1> to ⁇ 18>, wherein the specific range of the kinetic viscosity of the amino-modified silicone of component (D) at 25°C is preferably 20 to 10,000 mm2/s, more preferably 100 to 5,000 mm2 /s, and even more preferably 500 to 2,000 mm2 /s.
  • a hair treatment agent or a fiber treatment agent for head accessories according to any one of ⁇ 1> to ⁇ 19>, wherein the amino polyether-modified silicone of component (D) is preferably represented by the following general formula (5):
  • R 17 represents a hydrogen atom or a monovalent hydrocarbon group having 1 to 6 carbon atoms.
  • R 18 represents R 17 or E.
  • E represents a monovalent group represented by -R 19 -Z 2 (R 19 represents a single bond or a divalent hydrocarbon group having 1 to 20 carbon atoms, and Z 2 represents a primary to tertiary amino group-containing group or an ammonium group-containing group).
  • W represents a divalent saturated hydrocarbon group having 1 to 6 carbon atoms.
  • d is a number of 2 or more
  • e is a number of 1 or more
  • f is a number of 2 or more and 100 or less
  • g is a number of 1 or more.
  • x is a number of 2 or more and 10 or less.
  • the structural units in the parentheses may be bonded in any order, and may be bonded in a block or random form.
  • f C x H 2x O may be the same or different.
  • multiple R 17 , R 18 , E, and W may be the same or different.
  • ⁇ 22> The hair treatment agent or fiber treatment agent for head accessories according to any one of ⁇ 1> to ⁇ 21>, wherein the amino polyether-modified silicone of component (D) has a kinetic viscosity at 25°C of preferably 5,000 to 200,000 mm2 /s, more preferably 20,000 to 150,000 mm2 /s, and even more preferably 40,000 to 100,000 mm2 /s.
  • ⁇ 23> The hair treatment agent or fiber treatment agent for head accessories according to any one of ⁇ 1> to ⁇ 22>, wherein the content of component (D) is preferably 0.1 to 10 mass%, more preferably 0.4 to 7 mass%, and even more preferably 0.8 to 5 mass%.
  • a hair treatment agent or a fiber treatment agent for head ornament products according to any one of ⁇ 1> to ⁇ 23>, wherein the kinetic viscosity of the dimethicone component (E) at 25°C is preferably 500 to 1,000,000 mm2 /s, more preferably 1,000 to 500,000 mm2 /s, even more preferably 5,000 to 300,000 mm2 /s, still more preferably 10,000 to 200,000 mm2 /s, still more preferably 30,000 to 200,000 mm2 /s, and even more preferably 50,000 to 200,000 mm2/s.
  • the dimethicone component (E) at 25°C is preferably 500 to 1,000,000 mm2 /s, more preferably 1,000 to 500,000 mm2 /s, even more preferably 5,000 to 300,000 mm2 /s, still more preferably 10,000 to 200,000 mm2 /s, still more preferably 30,000 to 200,000 mm2 /s, and even more preferably 50,000 to 200,000 mm2/s.
  • ⁇ 25> The hair treatment agent or fiber treatment agent for head accessories according to any one of ⁇ 1> to ⁇ 24>, wherein the content of component (E) is preferably 0.1 to 10 mass%, more preferably 1 to 8 mass%, and even more preferably 2 to 6 mass%.
  • a hair treatment agent or a fiber treatment agent for a head accessory according to any one of ⁇ 1> to ⁇ 25>, preferably containing component (D) and component (E).
  • the hair treatment agent or fiber treatment agent for head accessories according to any one of ⁇ 1> to ⁇ 26>, wherein the total content of components (D) and (E) is preferably 1 to 12 mass%, more preferably 1 to 10 mass%, even more preferably 2 to 10 mass%, even more preferably 3 to 10 mass%, and even more preferably 5 to 8 mass% or more.
  • ⁇ 28> The hair treatment agent or fiber treatment agent for head accessories according to any one of ⁇ 1> to ⁇ 27>, wherein the mass ratio (E)/(D) of component (E) to component (D) is preferably 0.1 to 15, more preferably 1 to 10, even more preferably 2 to 7, and even more preferably 3.5 to 7.
  • a hair treatment agent or a fiber treatment agent for a head accessory product comprising one or more selected from the following components (A) to (C), as well as components (D) and (E), wherein the total content of components (D) and (E) is 1 to 10 mass%.
  • R 1 represents a linear or branched alkyl or alkenyl group having 6 to 24 carbon atoms
  • R 2 and R 3 may be the same or different, and represent an alkyl group having 1 to 6 carbon atoms or -(A 1 O) m H
  • a 1 represents an alkylene group having 2 to 4 carbon atoms
  • m represents a number from 1 to 6
  • a 1 Os may be the same or different, and the arrangement is arbitrary
  • Y represents a hydrogen atom or a hydroxyl group.
  • R 4 represents a linear or branched alkyl group having 17 to 21 carbon atoms
  • two R 5 represent the same alkyl group having 1 to 4 carbon atoms
  • n represents a number from 2 to 4.
  • R 6 represents a saturated or unsaturated, linear or branched alkyl group having 18 to 22 carbon atoms
  • R 10 represents a saturated or unsaturated, linear or branched alkyl chain having 18 to 21 carbon atoms, and a represents an integer of 1 to 4
  • R 7 , R 8 and R 9 independently represent an alkyl group having 1 to 4 carbon atoms or a hydroxylalkyl group having 1 to 4 carbon atoms
  • X - represents a chloride ion, a bromide ion, a methosulfate ion or an ethosulfate ion.
  • B 0.1 to 2.5% by mass of mono-long chain alkyl quaternary ammonium salt having an alkyl group with 16 carbon atoms
  • C Linear or branched chain saturated aliphatic alcohols having
  • a hair treatment agent or a fiber treatment agent for a head accessory product comprising one or more selected from the following components (A) to (C), as well as components (D) and (E), wherein the total content of components (D) and (E) is 1 to 10 mass%.
  • R 1 represents a linear or branched alkyl or alkenyl group having 6 to 24 carbon atoms
  • R 2 and R 3 may be the same or different, and represent an alkyl group having 1 to 6 carbon atoms or -(A 1 O) m H
  • a 1 represents an alkylene group having 2 to 4 carbon atoms
  • m represents a number from 1 to 6
  • a 1 Os may be the same or different, and the arrangement is arbitrary
  • Y represents a hydrogen atom or a hydroxyl group.
  • B 0.1 to 2.5% by mass of mono-long chain alkyl quaternary ammonium salt having an alkyl group with 16 carbon atoms
  • C Linear or branched chain saturated aliphatic alcohols having 12 to 22 carbon atoms: 5 to 10% by mass
  • D One or more modified silicones selected from the group consisting of amino-modified silicones represented by any one of the general formulas (1a) to (1d): (E) Dimethicone having
  • a hair treatment agent or a fiber treatment agent for a head accessory according to any one of ⁇ 29> to ⁇ 31>, wherein the mass ratio (B)/(A) of component (B) to component (A) is in the range of either 0.1 to 0.17 or 0.1 to 0.5.
  • the hair treatment agent or fiber treatment agent for head accessories according to any one of ⁇ 1> to ⁇ 32>, further comprising an organic acid or a salt thereof, the organic acid being preferably a carboxylic acid compound, more preferably a compound having a molecular weight of 500 or less, more preferably 200 or less, and even more preferably one or more selected from aliphatic monocarboxylic acids, aromatic monocarboxylic acids, aliphatic dicarboxylic acids, aromatic dicarboxylic acids, polycarboxylic acids, hydroxycarboxylic acids, and acidic amino acids.
  • the organic acid being preferably a carboxylic acid compound, more preferably a compound having a molecular weight of 500 or less, more preferably 200 or less, and even more preferably one or more selected from aliphatic monocarboxylic acids, aromatic monocarboxylic acids, aliphatic dicarboxylic acids, aromatic dicarboxylic acids, polycarboxylic acids, hydroxycarboxylic acids, and acidic amino
  • the organic acid is preferably at least one selected from the group consisting of acetic acid, propionic acid, butanoic acid, benzoic acid, malonic acid, succinic acid, glutaric acid, adipic acid, maleic acid, fumaric acid, phthalic acid, isophthalic acid, polyglutamic acid, lactic acid, malic acid, glycolic acid, hydroxyacrylic acid, glyceric acid, tartaric acid, citric acid, glutamic acid, and aspartic acid, more preferably at least one selected from the group consisting of succinic acid, lactic acid, malic acid, and glycolic acid, even more preferably at least one selected from the group consisting of succinic acid, malic acid, and lactic acid, and even more preferably at least one selected from malic acid and lactic acid.
  • the organic acid is preferably at least one selected from the group consisting of acetic acid, propionic acid, butanoic acid, benzoic acid, malonic acid, succinic acid, glut
  • the salt of the organic acid is preferably an alkali metal salt or alkaline metal salt of the organic acid, more preferably an alkali metal salt, more preferably at least one selected from the group consisting of sodium salts and potassium salts, and even more preferably a sodium salt.
  • the hair treatment agent or fiber treatment agent for head accessories according to any one of ⁇ 33> to ⁇ 35>, wherein the proportion of the organic acid salt in the total amount of the organic acid and the organic acid salt is preferably 50% by mass or less, more preferably 20% by mass or less, and even more preferably 5% by mass or less, calculated as the organic acid equivalent, and may be 0% by mass.
  • the hair treatment agent or fiber treatment agent for head accessories according to any one of ⁇ 1> to ⁇ 36>, further comprising an aromatic alcohol, preferably at least one selected from the group consisting of benzyl alcohol, phenoxyethanol, and 2-benzyloxyethanol.
  • the hair treatment agent or fiber treatment agent for head accessories according to ⁇ 37> wherein the content of the aromatic alcohol is preferably 0.01 to 2 mass%, more preferably 0.05 to 1 mass%, and even more preferably 0.1 to 0.5 mass%.
  • the hair treatment agent or fiber treatment agent for head accessories according to any one of ⁇ 1> to ⁇ 38>, wherein the content of cationic surfactants other than component (A) and component (B) is preferably 1 mass% or less, more preferably 0.5 mass% or less, even more preferably 0.1 mass% or less, and even more preferably 0 mass%.
  • the hair treatment agent or fiber treatment agent for head accessories according to any one of ⁇ 1> to ⁇ 39>, wherein the content of the anionic surfactant is preferably 0.5% by mass or less, more preferably 0.1% by mass or less, even more preferably 0.05% by mass or less, and even more preferably 0% by mass.
  • the hair treatment agent or fiber treatment agent for head accessories according to any one of ⁇ 1> to ⁇ 40>, having a pH of preferably 2.0 to 7.5, more preferably 2.5 to 6.5, and even more preferably 2.5 to 5.5.
  • ⁇ 42> The hair treatment agent or fiber treatment agent for head accessories according to any one of ⁇ 1> to ⁇ 41>, having a viscosity of preferably 500 to 100,000 mPa ⁇ s, more preferably 1,000 to 50,000 mPa ⁇ s, even more preferably 5,000 to 40,000 mPa ⁇ s, and even more preferably 10,000 to 30,000 mPa ⁇ s.
  • the hair treatment agent or fiber treatment agent for head accessories according to any one of ⁇ 1> to ⁇ 42>, which is preferably applied to hair or fibers for head accessories and then rinsed off before use.
  • the hair treatment agent or fiber treatment agent for head accessories according to any one of ⁇ 1> to ⁇ 43>, which is preferably used on dyed hair or fibers for head accessories.
  • a method for treating hair or fibers for head accessories comprising applying the hair treatment agent or fiber treatment agent for head accessories described in any one of ⁇ 1> to ⁇ 44> to dyed hair or fibers for head accessories, and rinsing the hair or fibers for head accessories with water.
  • Examples 1 to 19 and Comparative Examples 1 to 8 The hair conditioners shown in Tables 5 and 6 were prepared by the following manufacturing method, and the appearance was observed or the viscosity was measured, and the durability of the conditioning effect (combing force) on wet hair after the first wash and after the third wash was evaluated according to the following methods and criteria.
  • the contents shown in the tables are the active amounts.
  • Hair conditioners were prepared in the following manner using the components in the amounts shown in Tables 5 and 6. To obtain a total volume of 500 mL of hair conditioner, each component was mixed in an amount 5 times (mL) the amount shown in the table. In a 500 mL beaker containing water, cetrimonium chloride (component (B)) or steartrimonium chloride (component (B')), and lactic acid (40% of the total amount) were added and heated and stirred at 56 ° C. Next, a cationic surfactant (component (A) or (A')), a higher alcohol (component (C)), and benzyl alcohol were mixed in advance, and the oily phase obtained by dissolving at 76 ° C.
  • component (B)) cetrimonium chloride
  • component (B') steartrimonium chloride
  • lactic acid 50% of the total amount
  • the viscosity (30°C) of the hair conditioners shown in Tables 5 and 6 was measured using a B-type viscometer (manufactured by Toki Sangyo Co., Ltd., TVB-10) with a spindle of "TC", at 10 rpm, and for 1 minute when the viscosity was 10,000 mPa s or more, and using a BM-type viscometer (manufactured by Toki Sangyo Co., Ltd., TV-10) with a rotor of "No. 3", at 12 rpm, and for 1 minute when the viscosity was less than 10,000 mPa s.
  • a hair coloring agent (liquid 1 shown in Table 2 and liquid 2 shown in Table 3 were mixed at a ratio of 1:1.5) was applied to 30 g of Japanese hair tresses in a bath ratio of 1:1, left for 5 minutes, and then washed off.
  • the combing force when combing 30 times with a brush at a constant speed (once per second) was measured using the dynamic combing force method (Suzuki et al.; J. Soc. Cosmet. Chem. Japan. Vol. 27, No.1, pp. 11-13, 1993), and the average of the 30 measured values (maximum value) was calculated and used as an index for evaluating the durability of the conditioning effect.

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Abstract

The present invention provides a hair treatment agent or a head decoration product fiber treatment agent that can provide a continued lack of tangling and feeling of squeakiness in a wet state, even after repeated washing of the post-treatment hair or fibers. In other words, the present invention provides a hair treatment agent or a head decoration product fiber treatment agent containing ingredients (A)-(C), and one or more selected from among ingredients (D) and (E), wherein the total content of ingredients (D) and (E) is 1-15 mass%. (A) A cationic surfactant selected from among ether amines or salts thereof, amido amines or salts thereof, and mono long-chain alkyl quaternary ammonium salts that have an alkyl group having a carbon number of 18 or greater (B) A mono long-chain alkyl quaternary ammonium salt having a not-greater-than C16 alkyl group, 0.1-2.8 mass% (C) A higher alcohol, 1-15 mass% (D) A modified silicone selected from among amino-modified silicones and aminopolyether-modified silicones (E) Dimethicone

Description

毛髪処理剤又は頭飾製品用繊維処理剤Hair treatment agents or fiber treatment agents for head accessories
 本発明は、毛髪処理剤、又はかつら、エクステンション等の頭飾製品用繊維処理剤に関し、好適にはシャンプー洗髪後に使用される、ヘアリンス、ヘアコンディショナー、ヘアトリートメント、ヘアパック等の洗い流すタイプの毛髪化粧料に関する。 The present invention relates to a hair treatment agent or a fiber treatment agent for head accessories such as wigs and extensions, and is preferably a rinse-off type hair cosmetic product such as a hair rinse, hair conditioner, hair treatment, or hair pack that is used after shampooing.
 シャンプー洗髪後に用いられる、ヘアリンス、ヘアコンディショナー等の洗い流すタイプの毛髪化粧料は、カチオン界面活性剤や高級アルコールを主成分とし、毛髪に滑らかさやしっとり感を付与して毛髪の表面状態を整えることを目的としている。例えば、特許文献1~3には、カチオン界面活性剤、高級アルコール、シリコーン等を配合した、毛髪に好ましい感触を与える毛髪化粧料が開示されている。 Hair cosmetics that are used after shampooing, such as hair rinses and hair conditioners, contain cationic surfactants and higher alcohols as main ingredients and are intended to improve the condition of the hair surface by making the hair smooth and moisturized. For example, Patent Documents 1 to 3 disclose hair cosmetics that contain cationic surfactants, higher alcohols, silicones, etc. and give hair a pleasant feel.
 特許文献1では、特定のヒドロキシアミン、第4級アンモニウム塩、高級アルコール、数種の選択肢から選ばれるアミノ基含有シリコーン誘導体、及びメチルポリシロキサンを組み合わせた、毛髪にべたつきを与えることなく柔らかでしっとりした仕上がりを与え、すすぎ時の指通りと柔らかさに優れる毛髪化粧料が開示されている。 Patent Document 1 discloses a hair cosmetic that combines a specific hydroxylamine, a quaternary ammonium salt, a higher alcohol, an amino group-containing silicone derivative selected from several options, and a methylpolysiloxane, giving hair a soft, moist finish without stickiness, and providing excellent finger-combability and softness when rinsing.
 特許文献2では、アミノ基を含まない2種のシリコーンとアミノ基を含むシリコーンを併用し、第4級アンモニウム塩型カチオン界面活性剤と高融点脂肪族化合物を含むゲルマトリックスと混合してなる、滑らかな感触及び低減された摩擦などの改善されたコンディショニング効果を与えるヘアコンディショニング組成物が開示されている。 Patent Document 2 discloses a hair conditioning composition that combines two types of silicone that do not contain amino groups with a silicone that does contain amino groups, and mixes this with a gel matrix that contains a quaternary ammonium salt type cationic surfactant and a high melting point aliphatic compound, thereby providing improved conditioning effects such as a smooth feel and reduced friction.
 特許文献3では、第4級アンモニウム塩型カチオン性界面活性剤、高級アルコール、リン酸基含有シリコーン化合物及びアミノ変性シリコーン化合物を含有する、乳化安定性が良好で、毛髪のすべり感やまとまり感の持続に優れ、かつべたつき感が少ない毛髪化粧料が開示されている。 Patent Document 3 discloses a hair cosmetic composition that contains a quaternary ammonium salt cationic surfactant, a higher alcohol, a phosphate group-containing silicone compound, and an amino-modified silicone compound, and that has good emulsion stability, is excellent in maintaining the smoothness and manageability of hair, and is not sticky.
    (特許文献1)特許第5992257号公報
    (特許文献2)特表2007-522226号公報
    (特許文献3)特開2016-210686号公報
(Patent Document 1) Japanese Patent No. 5992257 (Patent Document 2) Japanese Patent Publication No. 2007-522226 (Patent Document 3) Japanese Patent Publication No. 2016-210686
 本発明は、次の成分(A)~(C)、並びに成分(D)及び成分(E)から選択される1種以上を含有し、成分(D)及び成分(E)の合計含有量が1質量%以上15質量%以下である、毛髪処理剤又は頭飾製品用繊維処理剤を提供するものである。
 (A) エーテルアミン又はその塩、アミドアミン又はその塩、及び炭素数18以上のアルキル基を有するモノ長鎖アルキル第4級アンモニウム塩からなる群より選ばれる1種以上のカチオン界面活性剤
 (B) 炭素数16以下のアルキル基を有するモノ長鎖アルキル第4級アンモニウム塩 0.1質量%以上2.8質量%以下
 (C) 高級アルコール 1質量%以上15質量%以下
 (D) アミノ変性シリコーン及びアミノポリエーテル変性シリコーンからなる群より選ばれる1種以上の変性シリコーン
 (E) ジメチコン
The present invention provides a hair treatment agent or a fiber treatment agent for a head accessory product, which contains one or more components selected from the following components (A) to (C), as well as components (D) and (E), and the total content of components (D) and (E) is 1% by mass or more and 15% by mass or less.
(A) One or more cationic surfactants selected from the group consisting of ether amines or their salts, amido amines or their salts, and mono-long-chain alkyl quaternary ammonium salts having an alkyl group with 18 or more carbon atoms. (B) Mono-long-chain alkyl quaternary ammonium salts having an alkyl group with 16 or less carbon atoms, 0.1% by mass or more and 2.8% by mass or less. (C) Higher alcohol, 1% by mass or more and 15% by mass or less. (D) One or more modified silicones selected from the group consisting of amino-modified silicones and aminopolyether-modified silicones. (E) Dimethicone.
 また本発明は、上記の毛髪処理剤又は頭飾製品用繊維処理剤を染色後の毛髪又は頭飾製品用繊維に塗布し、水で洗い流す毛髪処理方法を提供するものである。 The present invention also provides a hair treatment method in which the above-mentioned hair treatment agent or fiber treatment agent for head accessories is applied to dyed hair or fibers for head accessories and then rinsed off with water.
 特許文献1~3の記載によれば、これら文献に記載の毛髪化粧料は、仕上がり後の乾いた髪の感触やまとまり感の向上あるいは持続性に優れるものとされ、また特許文献1に記載の毛髪化粧料はすすぎ時の指通りと柔らかさに優れるものとされている。しかし、これら従来の毛髪化粧料では、処理後の毛髪を繰り返し洗髪した後、濡れた状態でのきしみ感や絡まりのなさを持続させることはできなかった。 According to Patent Documents 1 to 3, the hair cosmetics described in these documents are said to improve or sustain the feel and manageability of dry hair after finishing, and the hair cosmetic described in Patent Document 1 is said to be excellent in terms of runnability and softness when rinsing. However, these conventional hair cosmetics were unable to maintain the smooth feel and lack of tangles in the wet state after repeated washing of treated hair.
 したがって、本発明は、処理後の毛髪又は頭飾製品用繊維を繰り返し洗浄した後においても、濡れた状態でのきしみ感や絡まりのなさを持続させることができる毛髪処理剤又は頭飾製品用繊維処理剤に関する。また、使用感(べたつきのなさ)及び製剤安定性も良好な毛髪処理剤又は頭飾製品用繊維処理剤に関する。 Therefore, the present invention relates to a hair treatment agent or a fiber treatment agent for head accessories that can maintain the lack of squeaky feeling and tangling in a wet state even after the treated hair or fiber for head accessories has been repeatedly washed. The present invention also relates to a hair treatment agent or a fiber treatment agent for head accessories that has a good feel when used (non-sticky) and formulation stability.
 本発明者らは、毛髪処理剤又は頭飾製品用繊維処理剤、好適にはヘアリンス、ヘアコンディショナー等、シャンプー後に使用される洗い流すタイプの毛髪化粧料において、特定の2種のカチオン界面活性剤、高級アルコール、及び特定の2種のシリコーンを併用することにより、処理後の毛髪又は頭飾製品用繊維の濡れた状態でのきしみ感や絡まりのなさを持続させられることを見出した。また、毛髪処理剤又は頭飾製品用繊維処理剤の使用感(べたつきのなさ)及び製剤安定性も良好であることを見出した。 The inventors have discovered that by using two specific cationic surfactants, a higher alcohol, and two specific silicones in a hair treatment agent or a fiber treatment agent for head accessories, preferably a hair cosmetic product such as a hair rinse or hair conditioner that is used after shampooing and is rinsed off, the treated hair or fiber for head accessories can be made to retain its smooth, tangle-free feel when wet. They have also discovered that the feel of use (non-stickiness) and formulation stability of the hair treatment agent or fiber treatment agent for head accessories are good.
 本発明の毛髪処理剤又は頭飾製品用繊維処理剤は、処理後の毛髪又は頭飾製品用繊維を繰り返し洗浄した後においても、濡れた状態でのきしみ感や絡まりのなさを持続させることができ、また、毛髪処理剤又は頭飾製品用繊維処理剤の使用感(べたつきのなさ)及び製剤安定性にも優れる。 The hair treatment agent or fiber treatment agent for head accessories of the present invention can maintain the absence of squeaky feeling or tangles in a wet state even after the treated hair or fiber for head accessories has been repeatedly washed, and the hair treatment agent or fiber treatment agent for head accessories also has excellent feel when used (non-sticky) and formulation stability.
発明の詳細な説明Detailed Description of the Invention
 [定義]
 本明細書において、本発明の毛髪処理剤と頭飾製品用繊維処理剤とをまとめて「処理剤」ということがある。
 本明細書において、「毛髪」とは、主として頭髪を意味し、頭飾製品に用いられる毛髪も包含する。
 本明細書において、「頭飾製品」とは、例えば、ヘアーウィッグ、かつら、ウィービング、ヘアーエクステンション、ブレードヘアー、ヘアーアクセサリー、ドールヘアー等を意味する。
 本明細書において、「頭飾製品用繊維」とは、前記頭飾製品に用いられる繊維を意味する。
[Definition]
In this specification, the hair treatment agent of the present invention and the fiber treatment agent for head ornament products may be collectively referred to as the "treatment agent".
In this specification, "hair" primarily refers to hair on the head, and also includes hair used for head decoration products.
In this specification, the term "headwear product" refers to, for example, hair wigs, hairpieces, weaving, hair extensions, braided hair, hair accessories, doll hair, and the like.
In this specification, the term "fiber for head accessories" refers to a fiber used in the head accessories.
 <毛髪又は頭飾製品用繊維>
 本発明の処理剤の適用対象は、毛髪又は頭飾製品用繊維である。これらの中でも、毛髪がより好ましい。
 本発明の処理剤の適用対象となる頭飾製品用繊維としては、天然由来繊維、合成繊維のいずれでもよいが、天然由来繊維が好ましい。天然由来繊維とは、天然の動植物から採取した繊維、もしくはケラチン、コラーゲン、カゼイン、大豆、落花生、トウモロコシ、絹屑、絹蛋白質(例えば絹フィブロイン)等由来の蛋白質や多糖類等のポリマーやオリゴマーを原料として人工的に製造された繊維をいう。これらのうち、獣毛、人毛、又はケラチン、コラーゲン、カゼイン、大豆、落花生、トウモロコシ、絹屑、絹蛋白質(例えば絹フィブロイン)等由来の蛋白質や多糖類等のポリマーやオリゴマーを原料として人工的に製造された繊維が好ましく、ケラチン、コラーゲン、カゼイン、大豆蛋白質、落花生蛋白質、トウモロコシ蛋白質、絹蛋白質(例えば絹フィブロイン)等由来の蛋白質を原料とする再生蛋白質繊維がより好ましく、コラーゲンを原料とする再生コラーゲン繊維、絹フィブロインを原料とする再生絹繊維等の再生蛋白質繊維が更に好ましく、再生コラーゲン繊維がより更に好ましい。
 再生コラーゲン繊維は、公知の技術で製造することができる。再生コラーゲン繊維の組成はコラーゲン100%である必要はなく、品質改良のための天然ポリマー、合成ポリマー、添加剤等が含まれていてもよい。更には、再生コラーゲン繊維は後加工又は後処理されたものであってもよい。再生コラーゲン繊維の形態としては、フィラメントが好ましい。フィラメントは、一般にボビン巻きした状態のものや箱詰めした状態のものから取り出される。また、再生コラーゲン繊維の製造工程で乾燥工程から出てきたフィラメントを直接利用することもできる。
<Fibers for hair and head accessories>
The treatment agent of the present invention is applied to hair or fibers for head accessories, and among these, hair is more preferred.
The fibers for head ornament products to which the treatment agent of the present invention is applied may be either naturally derived fibers or synthetic fibers, but naturally derived fibers are preferred. Naturally derived fibers refer to fibers collected from natural animals and plants, or fibers artificially manufactured using polymers and oligomers such as proteins and polysaccharides derived from keratin, collagen, casein, soybeans, peanuts, corn, silk waste, silk protein (e.g., silk fibroin), etc. as raw materials. Among these, fibers artificially manufactured using polymers and oligomers such as proteins and polysaccharides derived from animal hair, human hair, or proteins and polysaccharides derived from keratin, collagen, casein, soybeans, peanuts, corn, silk waste, silk protein (e.g., silk fibroin), etc. as raw materials are preferred, regenerated protein fibers derived from proteins derived from keratin, collagen, casein, soybean protein, peanut protein, corn protein, silk protein (e.g., silk fibroin), etc. as raw materials are more preferred, regenerated protein fibers such as regenerated collagen fibers derived from collagen as raw materials, regenerated silk fibers derived from silk fibroin as raw materials, etc. are even more preferred, and regenerated collagen fibers are even more preferred.
Regenerated collagen fibers can be produced by known techniques. The composition of regenerated collagen fibers does not need to be 100% collagen, and may contain natural polymers, synthetic polymers, additives, etc. for quality improvement. Furthermore, regenerated collagen fibers may be post-processed or post-treated. The regenerated collagen fibers are preferably in the form of filaments. Filaments are generally taken out from bobbins or boxes. In addition, filaments coming out of the drying process in the manufacturing process of regenerated collagen fibers can also be used directly.
 合成繊維としては、合成樹脂を主成分として含む繊維が挙げられる。合成繊維の製造容易性の観点、及び頭髪に近い風合いを得る観点から、該合成樹脂は、好ましくは熱可塑性樹脂であり、より好ましくはポリエステル樹脂、ポリアミド樹脂、ポリイミド樹脂、ポリアミドイミド樹脂、塩化ビニル樹脂、ポリカーボネート樹脂、ポリフェニレンスルフィド樹脂、及びモダアクリル樹脂(アクリロニトリルと塩化ビニルの共重合体)からなる群より選ばれる1種以上である。ここでいう「主成分」とは、合成繊維中の含有量が、好ましくは50質量%以上、より好ましくは60質量%以上、更に好ましくは70質量%以上、より更に好ましくは80質量%以上、より更に好ましくは90質量%以上であって、100質量%以下の成分を意味する。
 合成繊維は、上記合成樹脂以外に、本発明の効果を阻害しない範囲で、更に難燃剤、難燃助剤、光又は熱安定剤、蛍光剤、酸化防止剤、静電防止剤、紫外線吸収剤等の各種成分を含有することができる。
The synthetic fiber may be a fiber containing a synthetic resin as a main component. From the viewpoint of ease of production of the synthetic fiber and of obtaining a texture similar to that of hair, the synthetic resin is preferably a thermoplastic resin, more preferably one or more selected from the group consisting of polyester resin, polyamide resin, polyimide resin, polyamideimide resin, vinyl chloride resin, polycarbonate resin, polyphenylene sulfide resin, and modacrylic resin (copolymer of acrylonitrile and vinyl chloride). The term "main component" as used herein means a component whose content in the synthetic fiber is preferably 50% by mass or more, more preferably 60% by mass or more, even more preferably 70% by mass or more, even more preferably 80% by mass or more, and even more preferably 90% by mass or more, but not more than 100% by mass.
In addition to the above synthetic resins, the synthetic fibers may further contain various components such as flame retardants, flame retardant assistants, light or heat stabilizers, fluorescent agents, antioxidants, antistatic agents, and ultraviolet absorbers, as long as the effects of the present invention are not impaired.
 〔成分(A):エーテルアミン又はその塩、アミドアミン又はその塩、及び炭素数18以上のアルキル基を有するモノ長鎖アルキル第4級アンモニウム塩からなる群より選ばれる1種以上のカチオン界面活性剤〕 [Component (A): One or more cationic surfactants selected from the group consisting of ether amines or their salts, amido amines or their salts, and mono-long-chain alkyl quaternary ammonium salts having an alkyl group with 18 or more carbon atoms]
 成分(A)は、濡れた状態でのきしみ感や絡まりのなさを持続させ、処理剤の使用感(べたつきのなさ)及び製剤安定性を向上させる観点から、好ましくはエーテルアミン又はその塩、及びアミドアミン又はその塩からなる群より選ばれる1種以上であり、より好ましくはエーテルアミン又はその塩を含むカチオン界面活性剤である。
 エーテルアミンとしては、下記一般式(1)で表される化合物が挙げられる。
From the viewpoints of maintaining the freedom from squeaky feeling and tangling in a wet state and improving the feel of the treatment agent in use (freedom from stickiness) and the formulation stability, component (A) is preferably one or more selected from the group consisting of etheramines or salts thereof, and amidoamines or salts thereof, and more preferably a cationic surfactant containing an etheramine or a salt thereof.
The ether amine may be a compound represented by the following general formula (1).
Figure JPOXMLDOC01-appb-C000001
Figure JPOXMLDOC01-appb-C000001
 〔式中、R1は、炭素数6~24の直鎖又は分岐鎖のアルキル基又はアルケニル基を示し、R2及びR3は、同一でも異なってもよく、炭素数1~6のアルキル基又は-(A1O)H(A1は炭素数2~4のアルキレン基を示し、mは1~6の数を示し、m個のA1Oは同一でも異なってもよく、その配列は任意である)を示す。Yは水素原子又は水酸基を示す。〕 [In the formula, R 1 represents a linear or branched alkyl or alkenyl group having 6 to 24 carbon atoms, R 2 and R 3 may be the same or different, and represent an alkyl group having 1 to 6 carbon atoms or -(A 1 O) m H (A 1 represents an alkylene group having 2 to 4 carbon atoms, m represents a number from 1 to 6, m A 1 Os may be the same or different, and the arrangement is arbitrary), and Y represents a hydrogen atom or a hydroxyl group.]
 エーテルアミン又はその塩の好ましい具体例としては、N,N-ジメチル-3-ヘキサデシルオキシプロピルアミン又はその塩、N,N-ジメチル-3-オクタデシルオキシプロピルアミン又はその塩、ヘキサデシルオキシ(2-ヒドロキシプロピル)ジメチルアミン又はその塩、オクタデシルオキシ(2-ヒドロキシプロピル)ジメチルアミン又はその塩等が挙げられる。なかでも、N,N-ジメチル-3-オクタデシルオキシプロピルアミン又はその塩、オクタデシルオキシ(2-ヒドロキシプロピル)ジメチルアミン又はその塩がより好ましい。 Specific preferred examples of etheramines or salts thereof include N,N-dimethyl-3-hexadecyloxypropylamine or salts thereof, N,N-dimethyl-3-octadecyloxypropylamine or salts thereof, hexadecyloxy(2-hydroxypropyl)dimethylamine or salts thereof, octadecyloxy(2-hydroxypropyl)dimethylamine or salts thereof, etc. Among these, N,N-dimethyl-3-octadecyloxypropylamine or salts thereof, and octadecyloxy(2-hydroxypropyl)dimethylamine or salts thereof are more preferred.
 アミドアミンとしては、下記一般式(2)で表される化合物が挙げられる。 An example of an amidoamine is a compound represented by the following general formula (2):
Figure JPOXMLDOC01-appb-C000002
Figure JPOXMLDOC01-appb-C000002
 〔式中、R4は炭素数17~21の直鎖又は分岐鎖のアルキル基を示し、2個のR5は同一の炭素数1~4のアルキル基を示し、nは2~4の数を示す。〕 [In the formula, R 4 represents a linear or branched alkyl group having 17 to 21 carbon atoms, two R 5 represent the same alkyl group having 1 to 4 carbon atoms, and n represents a number from 2 to 4.]
 アミドアミン又はその塩の好ましい具体例としては、ステアリン酸ジメチルアミノエチルアミド又はその塩、ステアリン酸ジメチルアミノプロピルアミド又はその塩、ステアリン酸ジエチルアミノエチルアミド又はその塩、ステアリン酸ジエチルアミノプロピルアミド又はその塩、ステアリン酸ジプロピルアミノエチルアミド又はその塩、ステアリン酸ジプロピルアミノプロピルアミド又はその塩、ベヘン酸ジメチルアミノプロピルアミド又はその塩、ベヘン酸ジエチルアミノプロピルアミド又はその塩等が挙げられる。なかでも、ステアリン酸ジメチルアミノプロピルアミド又はその塩、ステアリン酸ジエチルアミノエチルアミド又はその塩、ベヘン酸ジメチルアミノプロピルアミド又はその塩、ベヘン酸ジエチルアミノプロピルアミド又はその塩がより好ましい。 Specific preferred examples of amidoamines or their salts include dimethylaminoethyl stearate or its salts, dimethylaminopropyl stearate or its salts, diethylaminoethyl stearate or its salts, diethylaminopropyl stearate or its salts, dipropylaminoethyl stearate or its salts, dipropylaminopropyl stearate or its salts, dimethylaminopropyl stearate or its salts, dimethylaminopropyl stearate or its salts, diethyl .... Of these, dimethylaminopropyl stearate or its salts, diethylaminoethyl stearate or its salts, dimethylaminopropyl stearate or its salts, diethylaminopropyl stearate or its salts, dimethylaminopropyl stearate or its salts, diethylaminopropyl stearate or its salts, dimethylaminopropyl stearate or its salts, diethylaminopropyl stearate or its salts.
 エーテルアミン、アミドアミンの塩としては、有機酸又は無機酸による塩が挙げられる。無機酸としては、例えば、塩酸、硫酸、リン酸等による塩が挙げられる。有機酸としては、例えば、酢酸、プロピオン酸等のモノカルボン酸による塩;マロン酸、コハク酸、グルタル酸、アジピン酸、マレイン酸、フマル酸、フタル酸等のジカルボン酸による塩;ポリグルタミン酸等のポリカルボン酸による塩;グリコール酸、乳酸、ヒドロキシアクリル酸、グリセリン酸、リンゴ酸、酒石酸、クエン酸等のヒドロキシカルボン酸による塩;グルタミン酸、アスパラギン酸等の酸性アミノ酸による塩等が挙げられる。なかでも、無機酸塩としては塩酸による塩がより好ましい。有機酸塩としては、ジカルボン酸、ヒドロキシカルボン酸、酸性アミノ酸による塩が好ましい。ジカルボン酸による塩としては、マレイン酸、コハク酸による塩がより好ましい。ヒドロキシカルボン酸による塩としては、グリコール酸、乳酸、リンゴ酸による塩がより好ましい。酸性アミノ酸による塩としては、グルタミン酸による塩がより好ましい。 The salts of ether amines and amido amines include salts with organic or inorganic acids. Examples of inorganic acids include salts with hydrochloric acid, sulfuric acid, phosphoric acid, and the like. Examples of organic acids include salts with monocarboxylic acids such as acetic acid and propionic acid; salts with dicarboxylic acids such as malonic acid, succinic acid, glutaric acid, adipic acid, maleic acid, fumaric acid, and phthalic acid; salts with polycarboxylic acids such as polyglutamic acid; salts with hydroxycarboxylic acids such as glycolic acid, lactic acid, hydroxyacrylic acid, glyceric acid, malic acid, tartaric acid, and citric acid; and salts with acidic amino acids such as glutamic acid and aspartic acid. Among these, salts with hydrochloric acid are more preferred as inorganic acid salts. Examples of organic acid salts include salts with dicarboxylic acids, hydroxycarboxylic acids, and acidic amino acids. Examples of salts with dicarboxylic acids include salts with maleic acid and succinic acid. Examples of salts with hydroxycarboxylic acids include salts with glycolic acid, lactic acid, and malic acid. Examples of salts with acidic amino acids include salts with glutamic acid.
 炭素数18以上のアルキル基を有するモノ長鎖アルキル第4級アンモニウム塩としては、下記一般式(3)で表される化合物が挙げられる。  Examples of mono-long chain alkyl quaternary ammonium salts with an alkyl group having 18 or more carbon atoms include compounds represented by the following general formula (3).
Figure JPOXMLDOC01-appb-C000003
Figure JPOXMLDOC01-appb-C000003
 〔式中、R6は炭素数18~22の飽和若しくは不飽和の直鎖若しくは分岐鎖のアルキル基、R10-CO-NH-(CH2)a-又はR10-CO-O-(CH2)a-(R10は炭素数18~21の飽和又は不飽和の直鎖又は分岐鎖のアルキル鎖を示し、aは1~4の整数を示す)を示し、R7、R8及びR9は独立して、炭素数1~4のアルキル基、炭素数1~4のヒドロキシルアルキル基を示し、X-は塩化物イオン、臭化物イオン、メトサルフェートイオン又はエトサルフェートイオンを示す。〕 [In the formula, R 6 represents a saturated or unsaturated, linear or branched alkyl group having 18 to 22 carbon atoms, R 10 -CO-NH-(CH 2 ) a - or R 10 -CO-O-(CH 2 ) a - (R 10 represents a saturated or unsaturated, linear or branched alkyl chain having 18 to 21 carbon atoms, and a represents an integer of 1 to 4), R 7 , R 8 and R 9 independently represent an alkyl group having 1 to 4 carbon atoms or a hydroxylalkyl group having 1 to 4 carbon atoms, and X - represents a chloride ion, a bromide ion, a methosulfate ion or an ethosulfate ion.]
 好適な炭素数18以上のアルキル基を有するモノ長鎖アルキル第4級アンモニウム塩としては、例えば、ステアルトリモニウムクロリド、ステアルトリモニウムブロミド、ステアルトリモニウムメトサルフェート、ベヘントリモニウムクロリド、ベヘントリモニウムメトサルフェート、ベヘナミドプロピルトリモニウムクロリド、ベヘナミドプロピルトリモニウムメトサルフェート、べヘナミドプロピルエチルジモニウムエトサルフェート、ベヘナミドプロピルPGジモニウムクロリド等が挙げられる。 Suitable examples of mono-long chain alkyl quaternary ammonium salts having an alkyl group with 18 or more carbon atoms include steartrimonium chloride, steartrimonium bromide, steartrimonium methosulfate, behentrimonium chloride, behentrimonium methosulfate, behenamidopropyltrimonium chloride, behenamidopropyltrimonium methosulfate, behenamidopropyl ethyldimonium ethosulfate, behenamidopropyl PG dimonium chloride, etc.
 成分(A)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。本発明の処理剤中における成分(A)の含有量は、濡れた状態でのきしみ感や絡まりのなさを持続させ、処理剤の使用感(べたつきのなさ)及び製剤安定性を向上させる観点から、処理剤の使用感と安定性の観点から、好ましくは1質量%以上、より好ましくは1.5質量%以上、更に好ましくは2質量%以上であり、好ましくは10質量%以下、より好ましくは5質量%以下、更に好ましくは3質量%以下である。そして、本発明の処理剤中における成分(A)の含有量の具体的範囲は、好ましくは1~10質量%、より好ましくは1.5~5質量%、更に好ましくは2~3質量%である。 Component (A) may be used alone or in combination of two or more kinds. The content of component (A) in the treatment agent of the present invention is preferably 1% by mass or more, more preferably 1.5% by mass or more, even more preferably 2% by mass or more, from the viewpoint of maintaining the absence of squeaky feeling and tangling in a wet state, improving the feeling of use of the treatment agent (non-stickiness) and the formulation stability of the treatment agent, and is preferably 10% by mass or less, more preferably 5% by mass or less, even more preferably 3% by mass or less, from the viewpoint of the feeling of use and stability of the treatment agent. The specific range of the content of component (A) in the treatment agent of the present invention is preferably 1 to 10% by mass, more preferably 1.5 to 5% by mass, even more preferably 2 to 3% by mass.
 〔成分(B):炭素数16以下のアルキル基を有するモノ長鎖アルキル第4級アンモニウム塩〕
 成分(B)のモノ長鎖アルキル第4級アンモニウム塩のアルキル基は、濡れた状態でのきしみ感や絡まりのなさを持続させる観点から、炭素数12以上16以下であるものが好ましく、炭素数14以上16以下であるものがより好ましく、炭素数16のアルキル基であるものが更に好ましい。成分(B)の具体例としては、セトリモニウムクロリド、セトリモニウムブロミド、セトリモニウムメトサルフェート等が挙げられ、セトリモニウムクロリドが好ましい。
[Component (B): Mono-long chain alkyl quaternary ammonium salt having an alkyl group of 16 or less carbon atoms]
From the viewpoint of maintaining the absence of squeaky feeling and tangling in a wet state, the alkyl group of the mono long-chain alkyl quaternary ammonium salt of component (B) preferably has from 12 to 16 carbon atoms, more preferably from 14 to 16 carbon atoms, and even more preferably an alkyl group having 16 carbon atoms. Specific examples of component (B) include cetrimonium chloride, cetrimonium bromide, cetrimonium methosulfate, etc., with cetrimonium chloride being preferred.
 本発明の処理剤中における成分(B)の含有量は、濡れた状態でのきしみ感や絡まりのなさを持続させる観点から、0.1質量%以上であって、好ましくは0.2質量%以上、より好ましくは0.3質量%以上である。また、本発明の処理剤中における成分(B)の含有量は、処理剤の安定性の観点から、2.8質量%以下であって、好ましくは2.5質量%以下、より好ましくは2.3質量%以下である。そして、本発明の処理剤中における成分(B)の含有量の具体的範囲は、0.1~2.8質量%であって、好ましくは0.2~2.5質量%以上、より好ましくは0.3~2.3質量%である。 The content of component (B) in the treatment agent of the present invention is 0.1% by mass or more, preferably 0.2% by mass or more, and more preferably 0.3% by mass or more, from the viewpoint of maintaining the absence of squeaky feeling and tangling in a wet state. Also, the content of component (B) in the treatment agent of the present invention is 2.8% by mass or less, preferably 2.5% by mass or less, and more preferably 2.3% by mass or less, from the viewpoint of the stability of the treatment agent. The specific range of the content of component (B) in the treatment agent of the present invention is 0.1 to 2.8% by mass, preferably 0.2 to 2.5% by mass or more, and more preferably 0.3 to 2.3% by mass.
 本発明の処理剤中における成分(A)及び(B)の合計含有量は、濡れた状態でのきしみ感や絡まりのなさを持続させ、処理剤の使用感(べたつきのなさ)及び製剤安定性を向上させる観点から、好ましくは1.1質量%以上、より好ましくは1.7質量%以上、更に好ましくは2.3質量%以上であり、好ましくは12.8質量%以下、より好ましくは7.5質量%以下、更に好ましくは5.3質量%以下である。そして、本発明の処理剤中における成分(A)及び(B)の合計含有量の具体的範囲は、好ましくは1.1~12.8質量%、より好ましくは1.7~7.5質量%、更に好ましくは2.3~5.3質量%である。 The total content of components (A) and (B) in the treatment agent of the present invention is preferably 1.1% by mass or more, more preferably 1.7% by mass or more, even more preferably 2.3% by mass or more, from the viewpoint of maintaining the absence of squeaky feeling and tangling in a wet state and improving the feel of the treatment agent (non-stickiness) and the formulation stability, and is preferably 12.8% by mass or less, more preferably 7.5% by mass or less, even more preferably 5.3% by mass or less. The specific range of the total content of components (A) and (B) in the treatment agent of the present invention is preferably 1.1 to 12.8% by mass, more preferably 1.7 to 7.5% by mass, even more preferably 2.3 to 5.3% by mass.
 成分(A)に対する成分(B)の質量比(B)/(A)は、濡れた状態でのきしみ感や絡まりのなさを持続させ、処理剤の使用感(べたつきのなさ)及び製剤安定性を向上させる観点から、好ましくは0.01以上、より好ましくは0.05以上、更に好ましくは0.1以上であり、好ましくは1.2以下、より好ましくは1.1以下、更に好ましくは1.0以下、より更に好ましくは0.5以下である。そして、成分(A)に対する成分(B)の質量比(B)/(A)の具体的範囲は、好ましくは0.01~1.2、より好ましくは0.05~1.1、更に好ましくは0.1~1.0、より更に好ましくは0.1~0.5である。一方、毛髪又は頭飾製品用繊維への塗布性の向上、手や毛髪、頭飾製品用繊維からの垂れ落ちを防止する観点からは、質量比(B)/(A)は0.1~0.17の範囲が好ましい。 The mass ratio (B)/(A) of component (B) to component (A) is preferably 0.01 or more, more preferably 0.05 or more, even more preferably 0.1 or more, from the viewpoint of maintaining the absence of squeaky feeling and tangling in a wet state and improving the feeling of use of the treatment agent (non-stickiness) and the formulation stability, and is preferably 1.2 or less, more preferably 1.1 or less, even more preferably 1.0 or less, and even more preferably 0.5 or less. The specific range of the mass ratio (B)/(A) of component (B) to component (A) is preferably 0.01 to 1.2, more preferably 0.05 to 1.1, even more preferably 0.1 to 1.0, and even more preferably 0.1 to 0.5. On the other hand, from the viewpoint of improving the applicability to hair or fibers for head ornament products and preventing dripping from hands, hair, or fibers for head ornament products, the mass ratio (B)/(A) is preferably in the range of 0.1 to 0.17.
 〔成分(C):高級アルコール〕
 成分(C)の高級アルコールとしては、濡れた状態でのきしみ感や絡まりのなさを持続させ、製剤安定性を向上させる観点から、直鎖及び分岐鎖、また飽和及び不飽和のいずれの脂肪族アルコールでもよく、好ましくは直鎖又は分岐鎖の飽和脂肪族アルコールであり、より好ましくは直鎖飽和脂肪族アルコールである。成分(C)の高級アルコールの炭素数は、好ましくは12以上、より好ましくは14以上、更に好ましくは16以上であり、好ましくは22以下、より好ましくは20以下、更に好ましくは18以下である。そして、成分(C)の高級アルコールの炭素数の具体的範囲は、好ましくは12~22、より好ましくは14~20、更に好ましくは16~18である。
[Component (C): Higher alcohol]
From the viewpoint of maintaining the absence of squeaky feeling and tangling in a wet state and improving the formulation stability, the higher alcohol of component (C) may be either a linear or branched, saturated or unsaturated aliphatic alcohol, preferably a linear or branched saturated aliphatic alcohol, more preferably a linear saturated aliphatic alcohol. The number of carbon atoms of the higher alcohol of component (C) is preferably 12 or more, more preferably 14 or more, even more preferably 16 or more, and is preferably 22 or less, more preferably 20 or less, even more preferably 18 or less. The specific range of the number of carbon atoms of the higher alcohol of component (C) is preferably 12 to 22, more preferably 14 to 20, even more preferably 16 to 18.
 具体的には、成分(C)としては、ラウリルアルコール、ミリスチルアルコール、セチルアルコール、ステアリルアルコール、アラキルアルコール、ヘキシルデカノール、イソステアリルアルコール、オレイルアルコール、2-オクチルドデカノール等が挙げられる。なかでも、ステアリルアルコール、セチルアルコール、ミリスチルアルコールが好ましく、ステアリルアルコール、セチルアルコールがより好ましく、ステアリルアルコールが更に好ましい。これらの成分(C)は、いずれか1種を単独で、又は2種以上を組み合わせて使用することができる。 Specific examples of component (C) include lauryl alcohol, myristyl alcohol, cetyl alcohol, stearyl alcohol, arachyl alcohol, hexyldecanol, isostearyl alcohol, oleyl alcohol, and 2-octyldodecanol. Among these, stearyl alcohol, cetyl alcohol, and myristyl alcohol are preferred, stearyl alcohol and cetyl alcohol are more preferred, and stearyl alcohol is even more preferred. These components (C) can be used alone or in combination of two or more.
 本発明の処理剤中における成分(C)の含有量は、処理剤の安定性の観点から、1質量%以上であって、好ましくは3質量%以上、より好ましくは5質量%以上である。また、本発明の処理剤中における成分(C)の含有量は、塗布からすすぎ時及び乾燥後にかけての滑らかさの観点から、15質量%以下であって、好ましくは12質量%以下、より好ましくは10質量%以下である。そして、本発明の処理剤中における成分(C)の含有量の具体的範囲は、1~15質量%であって、好ましくは3~12質量%、より好ましくは5~10質量%以上である。 The content of component (C) in the treatment agent of the present invention is 1% by mass or more, preferably 3% by mass or more, and more preferably 5% by mass or more, from the viewpoint of the stability of the treatment agent. Also, the content of component (C) in the treatment agent of the present invention is 15% by mass or less, preferably 12% by mass or less, and more preferably 10% by mass or less, from the viewpoint of smoothness from application to rinsing and after drying. The specific range of the content of component (C) in the treatment agent of the present invention is 1 to 15% by mass, preferably 3 to 12% by mass, and more preferably 5 to 10% by mass or more.
 〔成分(D):アミノ変性シリコーン及びアミノポリエーテル変性シリコーンからなる群より選ばれる1種以上の変性シリコーン〕
 以下、アミノ変性シリコーンを「成分(D1)」、アミノポリエーテル変性シリコーンを「成分(D2)」とも表記する。
[Component (D): One or more modified silicones selected from the group consisting of amino-modified silicones and aminopolyether-modified silicones]
Hereinafter, the amino-modified silicone will also be referred to as "component (D1)" and the amino polyether-modified silicone will also be referred to as "component (D2)."
 <成分(D1):アミノ変性シリコーン>
 本明細書においてアミノ変性シリコーンとは、アミノ基を有し、かつポリエーテル構造を有さないシリコーンを意味する。成分(D1)としては、例えば下記一般式(4)で表されるアミノ変性シリコーンが挙げられる。
<Component (D1): Amino-modified silicone>
In this specification, the amino-modified silicone refers to a silicone that has an amino group and does not have a polyether structure. An example of the component (D1) is an amino-modified silicone represented by the following general formula (4).
Figure JPOXMLDOC01-appb-C000004
Figure JPOXMLDOC01-appb-C000004
 〔式中、R10はそれぞれ独立に、メチル基又はヒドロキシ基を示し、R11はそれぞれ独立に、炭素数1以上30以下のアルキル基、ヒドロキシ基、又はR12を示す。R12は-R13-Z1(R13は単結合、又は炭素数1以上20以下の2価の炭化水素基を示し、Z1は1~3級アミノ基含有基又はアンモニウム基含有基を示す)で表される1価の基を示す。aは0以上3000以下、bは1以上3000以下の数を示す。〕 [In the formula, R 10 each independently represents a methyl group or a hydroxy group, and R 11 each independently represents an alkyl group having 1 to 30 carbon atoms, a hydroxy group, or R 12. R 12 represents a monovalent group represented by -R 13 -Z 1 (R 13 represents a single bond or a divalent hydrocarbon group having 1 to 20 carbon atoms, and Z 1 represents a primary to tertiary amino group-containing group or an ammonium group-containing group). a represents a number of 0 to 3,000, and b represents a number of 1 to 3,000.]
 一般式(4)において、R10は好ましくはメチル基であり、R11は好ましくはメチル基又はR12である。 In formula (4), R 10 is preferably a methyl group, and R 11 is preferably a methyl group or R 12 .
 R13は、好ましくは炭素数1以上20以下の2価の炭化水素基、より好ましくは炭素数1以上20以下の2価の飽和炭化水素基、更に好ましくは炭素数1以上6以下の直鎖又は分岐鎖の2価の飽和炭化水素基、より更に好ましくはメチレン基、エチレン基、トリメチレン基、プロピレン基、テトラメチレン基、又はヘキサメチレン基、より更に好ましくはトリメチレン基又はプロピレン基である。 R13 is preferably a divalent hydrocarbon group having 1 to 20 carbon atoms, more preferably a divalent saturated hydrocarbon group having 1 to 20 carbon atoms, even more preferably a linear or branched divalent saturated hydrocarbon group having 1 to 6 carbon atoms, still more preferably a methylene group, ethylene group, trimethylene group, propylene group, tetramethylene group, or hexamethylene group, and even more preferably a trimethylene group or propylene group.
 Z1は、-N(R14)2、-NR14(CH2)cN(R15)2、又は-NR14(CH2)cN(R15)CO-R16で示されるアミノ基含有基であることが好ましい。ここで、R14及びR15はそれぞれ独立に水素原子又は炭素数1以上3以下のアルキル基を示し、好ましくは水素原子又はメチル基である。R16は炭素数1以上3以下のアルキル基を示す。cは1以上6以下の数を示し、好ましくは2以上4以下の数である。 Z 1 is preferably an amino group-containing group represented by -N(R 14 ) 2 , -NR 14 (CH 2 ) c N(R 15 ) 2 , or -NR 14 (CH 2 ) c N(R 15 )CO-R 16. Here, R 14 and R 15 each independently represent a hydrogen atom or an alkyl group having 1 to 3 carbon atoms, preferably a hydrogen atom or a methyl group. R 16 represents an alkyl group having 1 to 3 carbon atoms. c represents a number of 1 to 6, preferably a number of 2 to 4.
 一般式(4)において、R12は、好ましくは-(CH2)3-NH2、-(CH2)3-N(CH3)2、-(CH2)3-NH-(CH2)2-NH2、又は-(CH2)2-NH-(CH2)2-N(CH3)2であり、より好ましくは-(CH2)3-NH2又は-(CH2)3-NH-(CH2)2-NH2である。 In general formula (4), R 12 is preferably --(CH 2 ) 3 --NH 2 , --(CH 2 ) 3 --N(CH 3 ) 2 , --(CH 2 ) 3 --NH--(CH 2 ) 2 --NH 2 , or --(CH 2 ) 2 --NH--(CH 2 ) 2 --N(CH 3 ) 2 , and more preferably --(CH 2 ) 3 --NH 2 or --(CH 2 ) 3 --NH--(CH 2 ) 2 --NH 2 .
 一般式(4)で表されるアミノ変性シリコーンとしては、アモジメチコン、アミノプロピルジメチコン、ビス(アミノプロピル)ジメチコン、及びビス(セテアリル)アモジメチコンからなる群より選ばれる1種以上が好ましく、下記一般式(4a)~(4d)のいずれかで表される化合物がより好ましい。 The amino-modified silicone represented by general formula (4) is preferably one or more selected from the group consisting of amodimethicone, aminopropyl dimethicone, bis(aminopropyl) dimethicone, and bis(cetearyl) amodimethicone, and more preferably a compound represented by any of the following general formulas (4a) to (4d).
Figure JPOXMLDOC01-appb-C000005
 
Figure JPOXMLDOC01-appb-C000005
 
 〔式中、a、b、c及びR13は、前記と同じ意味を示す。〕
 成分(D1)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。塗布からすすぎ時及び乾燥後にかけての滑らかさの観点から、成分(D1)としては、上記一般式(4a)で表されるアミノ変性シリコーン(アモジメチコン)がより好ましい。
(In the formula, a, b, c and R 13 have the same meanings as defined above.)
Component (D1) may be used alone or in combination of two or more. From the viewpoint of smoothness from application to rinsing and after drying, component (D1) is more preferably an amino-modified silicone (amodimethicone) represented by the above general formula (4a).
 成分(D1)の25℃における動粘度は、塗布からすすぎ時及び乾燥後にかけての滑らかさの観点から、好ましくは20mm2/s以上、より好ましくは100mm2/s以上、更に好ましくは500mm2/s以上であり、好ましくは10,000mm2/s以下、より好ましくは5,000mm2/s以下、更に好ましくは2,000mm2/s以下である。そして、成分(D1)の25℃における動粘度の具体的範囲は、好ましくは20~10,000mm2/s、より好ましくは100~5,000mm2/s、更に好ましくは500~2,000mm2/sである。
 成分(D1)の動粘度は、25℃において、JIS Z8803:2011に規定されている“液体の粘度測定方法”、又はASTM D 445-46Tに準拠して測定される値であり、例えば、ウベローデ粘度計を用いて測定できる。
From the viewpoint of smoothness from application through rinsing and after drying, the kinetic viscosity of component (D1) at 25°C is preferably at least 20 mm 2 /s, more preferably at least 100 mm 2 /s, even more preferably at least 500 mm 2 /s, and is preferably at most 10,000 mm 2 /s, more preferably at most 5,000 mm 2 /s, even more preferably at most 2,000 mm 2 /s. The specific range of the kinetic viscosity of component (D1) at 25°C is preferably 20 to 10,000 mm 2 /s, more preferably 100 to 5,000 mm 2 /s, even more preferably 500 to 2,000 mm 2 /s.
The kinetic viscosity of component (D1) is a value measured at 25°C in accordance with the "Method for measuring viscosity of liquids" specified in JIS Z8803:2011 or ASTM D 445-46T, and can be measured, for example, using an Ubbelohde viscometer.
 成分(D1)として、市販のアミノ変性シリコーンを用いることもできる。例えば、一般式(4a)で表されるアミノ変性シリコーン(アモジメチコン)として、ダウ・東レ社製の「シリコーン SF 8457 C」等が挙げられる。 Commercially available amino-modified silicones can also be used as component (D1). For example, an amino-modified silicone (amodimethicone) represented by general formula (4a) is "Silicone SF 8457 C" manufactured by Dow-Toray.
 <成分(D2):アミノポリエーテル変性シリコーン>
 本明細書において、アミノポリエーテル変性シリコーンとは、アミノ基とポリエーテル構造とを有するシリコーンを意味する。
 成分(D2)におけるポリエーテル構造は、塗布からすすぎ時及び乾燥後にかけての滑らかさの観点から、好ましくはポリオキシアルキレン基である。
<Component (D2): Aminopolyether-modified silicone>
In this specification, aminopolyether-modified silicone means a silicone having an amino group and a polyether structure.
The polyether structure in component (D2) is preferably a polyoxyalkylene group from the viewpoint of smoothness from application through rinsing and after drying.
 塗布からすすぎ時及び乾燥後にかけての滑らかさの観点から、成分(D2)中のケイ素原子のモル数をSi、アルキレンオキシドの平均付加モル数をAOとした場合、その比率Si/AOは、好ましくは0.05以上、より好ましくは0.1以上、更に好ましくは0.3以上、より更に好ましくは0.5以上、より更に好ましくは0.7以上であり、好ましくは3.0以下、より好ましくは2.8以下、更に好ましくは2.6以下、より更に好ましくは2.4以下である。そして、成分(D2)における比率Si/AOの具体的範囲は、好ましくは0.05~3.0、より好ましくは0.1~2.8、更に好ましくは0.3~2.8、より更に好ましくは0.5~2.6、より更に好ましくは0.7~2.4である。
 Si/AOの比は、1H-NMR測定により測定される、ケイ素に結合した水素原子及び炭化水素基のHの積分値と、オキシアルキレン基のHの積分値とから算出できる。
From the viewpoint of smoothness from application to rinsing and after drying, where the number of moles of silicon atoms in component (D2) is Si and the average number of moles of alkylene oxide added is AO, the ratio Si/AO is preferably 0.05 or more, more preferably 0.1 or more, even more preferably 0.3 or more, still more preferably 0.5 or more, still more preferably 0.7 or more, and is preferably 3.0 or less, more preferably 2.8 or less, still more preferably 2.6 or less, and still more preferably 2.4 or less. The specific range of the ratio Si/AO in component (D2) is preferably 0.05 to 3.0, more preferably 0.1 to 2.8, even more preferably 0.3 to 2.8, still more preferably 0.5 to 2.6, and still more preferably 0.7 to 2.4.
The Si/AO ratio can be calculated from the integral value of hydrogen atoms bonded to silicon and H of hydrocarbon groups, and the integral value of H of oxyalkylene groups, measured by 1 H-NMR measurement.
 成分(D2)は、塗布からすすぎ時及び乾燥後にかけての滑らかさの観点から、窒素含有率が、好ましくは0.1質量%以上、より好ましくは0.2質量%以上、更に好ましくは0.5質量%以上、より更に好ましくは1.0質量%以上であり、好ましくは2.5質量%以下、より好ましくは2.0質量%以下、更に好ましくは1.8質量%以下、より更に好ましくは1.5質量%以下である。そして、成分(D2)の窒素含有率の具体的範囲は、好ましくは0.1~2.5質量%、より好ましくは0.2~2.0質量%、更に好ましくは0.5~1.8質量%、より更に好ましくは1.0~1.5質量%である。成分(D2)の窒素含有率は、JIS K0113:2005に規定されている電位差滴定方法に準拠して測定される値である。 From the viewpoint of smoothness from application to rinsing and after drying, the nitrogen content of component (D2) is preferably 0.1% by mass or more, more preferably 0.2% by mass or more, even more preferably 0.5% by mass or more, still more preferably 1.0% by mass or more, and preferably 2.5% by mass or less, more preferably 2.0% by mass or less, even more preferably 1.8% by mass or less, and even more preferably 1.5% by mass or less. The specific range of the nitrogen content of component (D2) is preferably 0.1 to 2.5% by mass, more preferably 0.2 to 2.0% by mass, even more preferably 0.5 to 1.8% by mass, and even more preferably 1.0 to 1.5% by mass. The nitrogen content of component (D2) is a value measured in accordance with the potentiometric titration method specified in JIS K0113:2005.
 成分(D2)は、好ましくは下記一般式(5)で表されるアミノポリエーテル変性シリコーンである。 Component (D2) is preferably an aminopolyether-modified silicone represented by the following general formula (5):
Figure JPOXMLDOC01-appb-C000006
Figure JPOXMLDOC01-appb-C000006
 〔式(5)中、R17は水素原子又は炭素数1以上6以下の1価の炭化水素基を示す。R18はR17又はEを示す。Eは-R19-Z2(R19は単結合、又は炭素数1以上20以下の2価の炭化水素基を示し、Z2は1~3級アミノ基含有基又はアンモニウム基含有基を示す)で表される1価の基を示す。Wは炭素数1以上6以下の2価の飽和炭化水素基を示す。
 dは2以上の数、eは1以上の数、fは2以上100以下の数、gは1以上の数を示す。xは2以上10以下の数を示す。括弧内の構造単位同士の結合順序は問わず、結合形態はブロック状でもランダム状でもよい。f個のCx2xOは、同一でも異なっていてもよい。また、複数個のR17、R18、E及びWは同一でも異なっていてもよい。〕
[In formula (5), R 17 represents a hydrogen atom or a monovalent hydrocarbon group having 1 to 6 carbon atoms. R 18 represents R 17 or E. E represents a monovalent group represented by -R 19 -Z 2 (R 19 represents a single bond or a divalent hydrocarbon group having 1 to 20 carbon atoms, and Z 2 represents a primary to tertiary amino group-containing group or an ammonium group-containing group). W represents a divalent saturated hydrocarbon group having 1 to 6 carbon atoms.
d is a number of 2 or more, e is a number of 1 or more, f is a number of 2 or more and 100 or less, and g is a number of 1 or more. x is a number of 2 or more and 10 or less. The structural units in the parentheses may be bonded in any order, and may be bonded in a block or random form. f C x H 2x O may be the same or different. In addition, multiple R 17 , R 18 , E, and W may be the same or different.
 なお、成分(D2)が一般式(5)で表されるアミノポリエーテル変性シリコーンである場合、前記Si/AOは、(d+e+1)/fで表される。 When component (D2) is an aminopolyether-modified silicone represented by general formula (5), the Si/AO is represented by (d+e+1)/f.
 一般式(5)において、R17は、好ましくは水素原子、炭素数1以上6以下のアルキル基、又はフェニル基、より好ましくはメチル基又はエチル基、更に好ましくはメチル基である。 In formula (5), R 17 is preferably a hydrogen atom, an alkyl group having 1 to 6 carbon atoms, or a phenyl group, more preferably a methyl group or an ethyl group, and even more preferably a methyl group.
 R19は、好ましくは炭素数1以上20以下の2価の炭化水素基、より好ましくは炭素数1以上20以下の2価の飽和炭化水素基、更に好ましくは炭素数1以上6以下の直鎖又は分岐鎖の2価の飽和炭化水素基、より更に好ましくはメチレン基、エチレン基、トリメチレン基、プロピレン基、テトラメチレン基、又はヘキサメチレン基、より更に好ましくはトリメチレン基又はプロピレン基である。 R 19 is preferably a divalent hydrocarbon group having 1 to 20 carbon atoms, more preferably a divalent saturated hydrocarbon group having 1 to 20 carbon atoms, even more preferably a linear or branched divalent saturated hydrocarbon group having 1 to 6 carbon atoms, still more preferably a methylene group, ethylene group, trimethylene group, propylene group, tetramethylene group, or hexamethylene group, and even more preferably a trimethylene group or propylene group.
 Z2は、-N(R20)2、-NR20(CH2)hN(R20)2、又は-NR20(CH2)hN(R21)CO-R22で示されるアミノ基含有基であることが好ましい。ここで、R20及びR21は、それぞれ独立に水素原子又は炭素数1以上3以下のアルキル基を示し、好ましくは水素原子又はメチル基である。R22は炭素数1以上3以下のアルキル基を示す。hは1以上6以下の数を示し、好ましくは2以上4以下の数である。 Z 2 is preferably an amino group-containing group represented by -N(R 20 ) 2 , -NR 20 (CH 2 ) h N(R 20 ) 2 , or -NR 20 (CH 2 ) h N(R 21 )CO-R 22. Here, R 20 and R 21 each independently represent a hydrogen atom or an alkyl group having 1 to 3 carbon atoms, and are preferably a hydrogen atom or a methyl group. R 22 represents an alkyl group having 1 to 3 carbon atoms. h represents a number of 1 to 6, and is preferably a number of 2 to 4.
 一般式(5)において、好ましいE基は、-(CH2)3-NH2、-(CH2)3-N(CH3)2、-(CH2)3-NH-(CH2)2-NH2、又は-(CH2)2-NH-(CH2)2-N(CH3)2であり、より好ましくは、-(CH2)3-NH-(CH2)2-NH2である。 In general formula (5), preferred E groups are -( CH2 ) 3 - NH2 , -( CH2 ) 3 -N( CH3 ) 2 , -( CH2 ) 3 -NH-( CH2 ) 2 -NH2, or -( CH2 ) 2 -NH-( CH2 ) 2 -N( CH3 ) 2 , and more preferably -( CH2 ) 3 -NH-( CH2 ) 2 - NH2 .
 一般式(5)において、Wは、エチレン基、プロピレン基、トリメチレン基、n-ブチレン基(テトラメチレン基)又はi-ブチレン基が好ましく、n-ブチレン基又はi-ブチレン基がより好ましい。ここでいうi-ブチレン基には、-CH(CH3)CH2CH2-、-CH2CH(CH3)CH2-、及び-CH2CH2CH(CH3)-が含まれる。 In formula (5), W is preferably an ethylene group, a propylene group, a trimethylene group, an n-butylene group (a tetramethylene group) or an i-butylene group, and more preferably an n-butylene group or an i - butylene group. The i- butylene group referred to here includes --CH( CH3 ) CH2CH2-- , --CH2CH ( CH3 ) CH2-- , and --CH2CH2CH ( CH3 )--.
 一般式(5)において、dは好ましくは2以上1000以下の数、より好ましくは2以上100以下の数である。eは好ましくは1以上50以下の数であり、fは好ましくは4以上50以下の数、より好ましくは10以上18以下の数であり、gは好ましくは1以上100以下の数である。 In general formula (5), d is preferably a number between 2 and 1000, more preferably between 2 and 100. e is preferably a number between 1 and 50, f is preferably a number between 4 and 50, more preferably between 10 and 18, and g is preferably a number between 1 and 100.
 一般式(5)において、xは、好ましくは2以上6以下、より好ましくは2以上4以下の数である。 In general formula (5), x is preferably a number from 2 to 6, more preferably from 2 to 4.
 成分(D2)は、より好ましくは下記一般式(5a)で表されるアミノポリエーテル変性シリコーンである。 Component (D2) is more preferably an aminopolyether-modified silicone represented by the following general formula (5a):
Figure JPOXMLDOC01-appb-C000007
Figure JPOXMLDOC01-appb-C000007
 〔式(5a)中、d~gは前記と同じ意味を示す。〕 [In formula (5a), d to g have the same meanings as above.]
 成分(D2)の25℃における動粘度は、塗布からすすぎ時及び乾燥後にかけての滑らかさの観点から、好ましくは5,000mm2/s以上、より好ましくは20,000mm2/s以上、更に好ましくは40,000mm2/s以上であり、好ましくは200,000mm2/s以下、より好ましくは150,000mm2/s以下、更に好ましくは100,000mm2/s以下である。そして、成分(D2)の25℃における動粘度の具体的範囲は、好ましくは5,000~200,000mm2/s、より好ましくは20,000~150,000mm2/s、更に好ましくは40,000~100,000mm2/sである。
 成分(D2)の動粘度は、成分(D1)と同様の方法で測定できる。
From the viewpoint of smoothness from application through rinsing and after drying, the kinetic viscosity of component (D2) at 25°C is preferably at least 5,000 mm 2 /s, more preferably at least 20,000 mm 2 /s, even more preferably at least 40,000 mm 2 /s, and is preferably at most 200,000 mm 2 /s, more preferably at most 150,000 mm 2 /s, even more preferably at most 100,000 mm 2 /s. The specific range of the kinetic viscosity of component (D2) at 25°C is preferably 5,000 to 200,000 mm 2 /s, more preferably 20,000 to 150,000 mm 2 /s, even more preferably 40,000 to 100,000 mm 2 /s.
The kinematic viscosity of component (D2) can be measured in the same manner as for component (D1).
 成分(D2)として、市販のアミノポリエーテル変性シリコーンを用いることもできる。例えば、一般式(5a)で表されるアミノポリエーテル変性シリコーンとして、ダウ・東レ社製の「DOWSIL SS-3588 FLUID」((ビスイソブチルPEG-15/アモジメチコン)コポリマー、Si/AO=2.39、窒素含有率:1.0質量%、有効成分量:71.5質量%)、「DOWSIL SILSTYLE 104」((ビスイソブチルPEG-14/アモジメチコン)コポリマー、窒素含有率:1.2質量%、Si/AO=2.46)、「DOWSIL SILSTYLE 201」((ビスイソブチルPEG-14/アモジメチコン)コポリマー、窒素含有率:1.2質量%、Si/AO=0.80)等が挙げられる。 Commercially available aminopolyether-modified silicones can also be used as component (D2). For example, examples of aminopolyether-modified silicones represented by general formula (5a) include "DOWSIL SS-3588 FLUID" (bisisobutyl PEG-15/amodimethicone copolymer, Si/AO=2.39, nitrogen content: 1.0% by mass, active ingredient content: 71.5% by mass), "DOWSIL SILSTYLE 104" (bisisobutyl PEG-14/amodimethicone copolymer, nitrogen content: 1.2% by mass, Si/AO=2.46), and "DOWSIL SILSTYLE 201" (bisisobutyl PEG-14/amodimethicone copolymer, nitrogen content: 1.2% by mass, Si/AO=0.80), all manufactured by Dow-Toray.
 成分(D)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。
 上記の中でも、成分(D)としては、塗布からすすぎ時及び乾燥後にかけての滑らかさを向上させ、濡れた状態でのきしみ感や絡まりのなさを持続させる観点から、好ましくは、前記一般式(4)で表されるアミノ変性シリコーン及び前記一般式(5)で表されるアミノポリエーテル変性シリコーンからなる群より選ばれる1種以上であり、より好ましくは、前記一般式(4a)で表されるアミノ変性シリコーン及び前記一般式(5a)で表されるアミノポリエーテル変性シリコーンからなる群より選ばれる1種以上であり、更に好ましくは前記一般式(4a)で表されるアミノ変性シリコーンである。
Component (D) may be used alone or in combination of two or more types.
Among the above, from the viewpoints of improving the smoothness from application to rinsing and after drying, and maintaining the absence of squeaky feeling and tangling in a wet state, component (D) is preferably one or more selected from the group consisting of the amino-modified silicone represented by general formula (4) and the amino polyether-modified silicone represented by general formula (5), more preferably one or more selected from the group consisting of the amino-modified silicone represented by general formula (4a) and the amino polyether-modified silicone represented by general formula (5a), and even more preferably the amino-modified silicone represented by general formula (4a).
 本発明の処理剤中における成分(D)の含有量は、塗布からすすぎ時及び乾燥後にかけての滑らかさの向上、濡れた状態でのきしみ感や絡まりのなさを持続させる観点から、好ましくは0.1質量%以上、より好ましくは0.4質量%以上、更に好ましくは0.8質量%以上であり、好ましくは10質量%以下、より好ましくは7質量%以下、更に好ましくは5質量%以下である。そして、本発明の処理剤中における成分(D)の含有量の具体的範囲は、好ましくは0.1~10質量%、より好ましくは0.4~7質量%、更に好ましくは0.8~5質量%である。 The content of component (D) in the treatment agent of the present invention is preferably 0.1% by mass or more, more preferably 0.4% by mass or more, even more preferably 0.8% by mass or more, and is preferably 10% by mass or less, more preferably 7% by mass or less, even more preferably 5% by mass or less, from the viewpoint of improving smoothness from application to rinsing and after drying, and maintaining the lack of squeaky feeling and tangling in a wet state. The specific range of the content of component (D) in the treatment agent of the present invention is preferably 0.1 to 10% by mass, more preferably 0.4 to 7% by mass, even more preferably 0.8 to 5% by mass.
 〔成分(E):ジメチコン〕
 成分(E)のジメチコンとしては、低揮発性であることが好ましく、その観点から、25℃における動粘度は、好ましくは500mm2/s以上、より好ましくは1,000mm2/s以上、更に好ましくは5,000mm2/s以上、より更に好ましくは1万mm2/s以上、より更に好ましくは3万mm2/s以上、より更に好ましくは5万mm2/s以上であり、好ましくは100万mm2/s以下、より好ましくは50万mm2/s以下、更に好ましくは30万mm2/s以下、より更に好ましくは20万mm2/s以下である。そして、成分(E)のジメチコンの25℃における動粘度は、好ましくは500~100万mm2/s、より好ましくは1,000~50万mm2/s、更に好ましくは5,000~30万mm2/s、より更に好ましくは1万~20万mm2/s、より更に好ましくは3万~20万mm2/s、より更に好ましくは5万~20万mm2/sである。なお、動粘度の異なる2種以上のジメチコンを用いた場合は、それら混合物としての粘度とする。
 成分(E)の動粘度は、25℃において、JIS Z8803:2011に規定されている“液体の粘度測定方法”、又はASTM D 445-46Tに準拠して測定される値であり、例えば、ウベローデ粘度計を用いて測定できる。
[Ingredient (E): Dimethicone]
The dimethicone component (E) is preferably low volatility, and from this viewpoint, the kinematic viscosity at 25°C is preferably 500 mm2/s or more, more preferably 1,000 mm2 /s or more, even more preferably 5,000 mm2/s or more, even more preferably 10,000 mm2 /s or more, even more preferably 30,000 mm2 /s or more, even more preferably 50,000 mm2 /s or more, and preferably 1,000,000 mm2 /s or less, more preferably 50,000 mm2 /s or less, even more preferably 300,000 mm2 /s or less, and even more preferably 200,000 mm2 /s or less. The kinetic viscosity of dimethicone in component (E) at 25°C is preferably 500 to 1,000,000 mm2 /s, more preferably 1,000 to 500,000 mm2 /s, even more preferably 5,000 to 300,000 mm2 /s, still more preferably 10,000 to 200,000 mm2 /s, still more preferably 30,000 to 200,000 mm2 /s, and even more preferably 50,000 to 200,000 mm2 /s. When two or more types of dimethicone with different kinetic viscosities are used, the viscosity is taken as the viscosity of the mixture.
The kinetic viscosity of component (E) is a value measured at 25°C according to the "Method for measuring viscosity of liquids" specified in JIS Z8803:2011 or in accordance with ASTM D 445-46T, and can be measured, for example, using an Ubbelohde viscometer.
 成分(E)として、市販のアミノ変性シリコーンを用いることもできる。例えば、ジメチコンとして、シリコーン KHS-3(動粘度10万~15万mm2/s(25℃))、シリコーン KHS-9(動粘度5000~25000mm2/s(25℃))(いずれも信越化学工業社製)等が挙げられる。 Commercially available amino-modified silicones can also be used as component (E). Examples of dimethicone include Silicone KHS-3 (dynamic viscosity 100,000 to 150,000 mm2 /s (25°C)) and Silicone KHS-9 (dynamic viscosity 5,000 to 25,000 mm2 /s (25°C)) (both manufactured by Shin-Etsu Chemical Co., Ltd.).
 本発明の処理剤中における成分(E)の含有量は、塗布からすすぎ時及び乾燥後にかけての滑らかさを向上させ、濡れた状態でのきしみ感や絡まりのなさを持続させる観点から、好ましくは0.1質量%以上、より好ましくは1質量%以上、更に好ましくは2質量%以上であり、好ましくは10質量%以下、より好ましくは8質量%以下、更に好ましくは6質量%以下である。そして、本発明の処理剤中における成分(E)の含有量の具体的範囲は、好ましくは0.1~10質量%、より好ましくは1~8質量%、更に好ましくは2~6質量%である。 The content of component (E) in the treatment agent of the present invention is preferably 0.1% by mass or more, more preferably 1% by mass or more, even more preferably 2% by mass or more, and is preferably 10% by mass or less, more preferably 8% by mass or less, even more preferably 6% by mass or less, from the viewpoint of improving smoothness from application to rinsing and after drying, and maintaining a lack of squeaky feeling and tangling in a wet state. The specific range of the content of component (E) in the treatment agent of the present invention is preferably 0.1 to 10% by mass, more preferably 1 to 8% by mass, even more preferably 2 to 6% by mass.
 本発明の処理剤において、成分(D)及び成分(E)はいずれか1種以上を含有すればよいが、成分(D)及び成分(E)の双方を含有することが好ましい。成分(D)及び(E)の合計含有量は、塗布からすすぎ時及び乾燥後にかけての滑らかさを向上させ、濡れた状態でのきしみ感や絡まりのなさを持続させる観点から、1質量%以上であって、好ましくは2質量%以上、より好ましくは3質量%以上、更に好ましくは5質量%以上であり、15質量%以下であって、好ましくは12質量%以下、より好ましくは10質量%以下、更に好ましくは8質量%以下である。そして、成分(D)及び(E)の合計含有量の具体的範囲は、1~15質量%であって、好ましくは1~12質量%、より好ましくは1~10質量%、更に好ましくは2~10質量%、より更に好ましくは3~10質量%、より更に好ましくは5~8質量%以上である。 The treatment agent of the present invention may contain at least one of components (D) and (E), but it is preferable to contain both components (D) and (E). The total content of components (D) and (E) is 1% by mass or more, preferably 2% by mass or more, more preferably 3% by mass or more, even more preferably 5% by mass or more, and 15% by mass or less, preferably 12% by mass or less, more preferably 10% by mass or less, even more preferably 8% by mass or less, from the viewpoint of improving smoothness from application to rinsing and after drying, and maintaining the lack of squeaky feeling and tangling in a wet state. The specific range of the total content of components (D) and (E) is 1 to 15% by mass, preferably 1 to 12% by mass, more preferably 1 to 10% by mass, even more preferably 2 to 10% by mass, even more preferably 3 to 10% by mass, even more preferably 5 to 8% by mass or more.
 成分(D)に対する成分(E)の質量比(E)/(D)は、塗布からすすぎ時及び乾燥後にかけての滑らかさを向上させ、濡れた状態でのきしみ感や絡まりのなさを持続させる観点から、好ましくは0.1以上、より好ましくは1以上、更に好ましくは2以上、より更に好ましくは3.5以上であり、好ましくは15以下、より好ましくは10以下、更に好ましくは7以下である。そして、成分(D)に対する成分(E)の質量比(E)/(D)の具体的範囲は、好ましくは0.1~15、より好ましくは1~10、更に好ましくは2~7、より更に好ましくは3.5~7である。 The mass ratio (E)/(D) of component (E) to component (D) is preferably 0.1 or more, more preferably 1 or more, even more preferably 2 or more, and even more preferably 3.5 or more, and is preferably 15 or less, more preferably 10 or less, and even more preferably 7 or less, from the viewpoint of improving smoothness from application to rinsing and after drying, and maintaining the lack of squeaky feeling and tangling in a wet state. The specific range of the mass ratio (E)/(D) of component (E) to component (D) is preferably 0.1 to 15, more preferably 1 to 10, even more preferably 2 to 7, and even more preferably 3.5 to 7.
 〔有機酸又はその塩〕
 本発明の処理剤には、更に有機酸又はその塩を含有することが好ましい。有機酸又はその塩は毛髪又は頭飾製品用繊維の内部改質成分として機能し、より滑らかな櫛通り性を得ることができる。有機酸としては、カルボン酸系化合物が挙げられ、好ましくは分子量が500以下、より好ましくは200以下の化合物である。
[Organic acid or its salt]
The treatment agent of the present invention preferably further contains an organic acid or a salt thereof. The organic acid or the salt thereof functions as an internal modifying component for hair or fibers for head accessories, and can provide smoother combing properties. The organic acid includes carboxylic acid compounds, preferably compounds having a molecular weight of 500 or less, more preferably 200 or less.
 カルボン酸系化合物としては、例えば、酢酸、プロピオン酸、ブタン酸等の炭素数4以下の脂肪族モノカルボン酸;安息香酸等の芳香族モノカルボン酸;マロン酸、コハク酸、グルタル酸、アジピン酸、マレイン酸、フマル酸等の脂肪族ジカルボン酸;フタル酸、イソフタル酸等の芳香族ジカルボン酸;ポリグルタミン酸等のポリカルボン酸;乳酸、リンゴ酸、グリコール酸、ヒドロキシアクリル酸、グリセリン酸、酒石酸、クエン酸等のヒドロキシカルボン酸;グルタミン酸、アスパラギン酸等の酸性アミノ酸などが挙げられ、これらのいずれかを単独で、又は2種以上を組み合わせて使用することができる。 Carboxylic acid compounds include, for example, aliphatic monocarboxylic acids having 4 or less carbon atoms, such as acetic acid, propionic acid, butanoic acid, etc.; aromatic monocarboxylic acids, such as benzoic acid; aliphatic dicarboxylic acids, such as malonic acid, succinic acid, glutaric acid, adipic acid, maleic acid, fumaric acid, etc.; aromatic dicarboxylic acids, such as phthalic acid, isophthalic acid, etc.; polycarboxylic acids, such as polyglutamic acid; hydroxycarboxylic acids, such as lactic acid, malic acid, glycolic acid, hydroxyacrylic acid, glyceric acid, tartaric acid, citric acid, etc.; acidic amino acids, such as glutamic acid, aspartic acid, etc. Any of these can be used alone or in combination of two or more.
 塗布からすすぎ時及び乾燥後にかけての滑らかさの観点から、好ましくはコハク酸、乳酸、リンゴ酸及びグリコール酸からなる群より選ばれる1種以上、より好ましくはコハク酸、リンゴ酸及び乳酸からなる群より選ばれる1種以上、更に好ましくはリンゴ酸及び乳酸から選ばれる1種以上である。 From the viewpoint of smoothness from application to rinsing and after drying, it is preferably one or more selected from the group consisting of succinic acid, lactic acid, malic acid and glycolic acid, more preferably one or more selected from the group consisting of succinic acid, malic acid and lactic acid, and even more preferably one or more selected from malic acid and lactic acid.
 なお有機酸は、配合時には、少なくとも一部が有機酸塩の状態であってもよい。有機酸の塩としては、毛髪化粧料に用いる場合の安全性の観点、及び入手容易性の観点から、有機酸のアルカリ金属塩又はアルカリ金属塩が好ましく、アルカリ金属塩がより好ましく、ナトリウム塩及びカリウム塩からなる群より選ばれる1種以上が更に好ましく、ナトリウム塩がより更に好ましい。 The organic acid may be at least partially in the form of an organic acid salt when blended. As the salt of the organic acid, from the viewpoint of safety when used in hair cosmetics and from the viewpoint of easy availability, an alkali metal salt or alkaline metal salt of the organic acid is preferred, an alkali metal salt is more preferred, one or more selected from the group consisting of sodium salts and potassium salts is even more preferred, and a sodium salt is even more preferred.
 有機酸及び有機酸塩の総量中における有機酸塩の割合は、くし通り性向上の観点から、好ましくは50質量%以下、より好ましくは20質量%以下、更に好ましくは5質量%以下であり、0質量%であってもよい。なお、ここでいう有機酸塩の割合は、有機酸塩量を有機酸量に換算して計算する。 From the viewpoint of improving combability, the proportion of organic acid salts in the total amount of organic acids and organic acid salts is preferably 50% by mass or less, more preferably 20% by mass or less, and even more preferably 5% by mass or less, and may be 0% by mass. The proportion of organic acid salts referred to here is calculated by converting the amount of organic acid salts into the amount of organic acid.
 本発明の処理剤中における有機酸の含有量は、くし通り性向上の観点から、好ましくは0.1質量%以上、より好ましくは0.5質量%以上、更に好ましくは1質量%以上であり、好ましくは5質量%以下、より好ましくは3質量%以下、更に好ましくは2質量%以下である。そして、本発明の処理剤中における有機酸の含有量の具体的範囲は、好ましくは0.1~5質量%、より好ましくは0.5~3質量%、更に好ましくは1~2質量%である。 From the viewpoint of improving combability, the content of the organic acid in the treatment agent of the present invention is preferably 0.1% by mass or more, more preferably 0.5% by mass or more, even more preferably 1% by mass or more, and preferably 5% by mass or less, more preferably 3% by mass or less, even more preferably 2% by mass or less. The specific range of the content of the organic acid in the treatment agent of the present invention is preferably 0.1 to 5% by mass, more preferably 0.5 to 3% by mass, even more preferably 1 to 2% by mass.
 〔芳香族アルコール〕
 本発明の処理剤には、更に芳香族アルコールを含有することが好ましい。芳香族アルコールは、毛髪又は頭飾製品用繊維の内部改質成分として機能する有機酸の毛髪又は頭飾製品用繊維の内部への浸透を促進する観点から使用され、例えば、ベンジルアルコール、フェノキシエタノール、2-ベンジルオキシエタノールが挙げられる。これらはいずれかを単独で又は2種類以上を組み合わせて使用することができる。
[Aromatic alcohol]
The treatment agent of the present invention preferably further contains an aromatic alcohol. The aromatic alcohol is used from the viewpoint of promoting the penetration of the organic acid, which functions as an internal modifying component of the hair or the fiber for head ornament products, into the inside of the hair or the fiber for head ornament products, and examples thereof include benzyl alcohol, phenoxyethanol, and 2-benzyloxyethanol. Any of these may be used alone or in combination of two or more kinds.
 本発明の処理剤中における芳香族アルコールの含有量は、有機酸の毛髪又は頭飾製品用繊維の内部への浸透を促進する観点から、好ましくは0.01質量%以上、より好ましくは0.05質量%以上、更に好ましくは0.1質量%以上であり、好ましくは2質量%以下、より好ましくは1質量%以下、更に好ましくは0.5質量%以下である。そして、本発明の処理剤中における芳香族アルコールの含有量の具体的範囲は、好ましくは0.01~2質量%、より好ましくは0.05~1質量%、更に好ましくは0.1~0.5質量%である。 The content of aromatic alcohol in the treatment agent of the present invention is preferably 0.01% by mass or more, more preferably 0.05% by mass or more, even more preferably 0.1% by mass or more, from the viewpoint of promoting the penetration of organic acid into the interior of hair or fibers for head accessories, and is preferably 2% by mass or less, more preferably 1% by mass or less, even more preferably 0.5% by mass or less. The specific range of the content of aromatic alcohol in the treatment agent of the present invention is preferably 0.01 to 2% by mass, more preferably 0.05 to 1% by mass, even more preferably 0.1 to 0.5% by mass.
 〔成分(A)及び成分(B)以外のカチオン界面活性剤〕
 本発明の処理剤には、毛髪処理剤又は頭飾製品用繊維処理剤として好適な粘度とし、使用感を向上させる観点から、成分(A)及び成分(B)以外のカチオン界面活性剤を適宜含有させることができる。ただし、濡れた状態でのきしみ感や絡まりのなさを持続させる観点からは、処理剤中における成分(A)及び成分(B)以外のカチオン界面活性剤の含有量は、1質量%以下が好ましく、0.5質量%以下がより好ましく、0.1質量%以下が更に好ましく、成分(A)及び成分(B)以外のカチオン界面活性剤を実質的に含有しないことがより更に好ましい。
[Cationic surfactants other than components (A) and (B)]
The treatment agent of the present invention may contain an appropriate cationic surfactant other than components (A) and (B) from the viewpoints of imparting a suitable viscosity as a hair treatment agent or a fiber treatment agent for head ornament products and improving the feeling of use. However, from the viewpoints of maintaining the feeling of squeaking and lack of tangling in a wet state, the content of the cationic surfactant other than components (A) and (B) in the treatment agent is preferably 1% by mass or less, more preferably 0.5% by mass or less, even more preferably 0.1% by mass or less, and even more preferably the treatment agent is substantially free of cationic surfactants other than components (A) and (B).
 〔アニオン界面活性剤〕
 本発明の処理剤には、成分(A)及び(B)のカチオン界面活性剤を含有しているため、過剰にアニオン界面活性剤を配合した場合には、カチオン界面活性剤とアニオン界面活性剤とが凝集物を形成してしまう可能性がある。このため、処理剤中におけるアニオン界面活性剤の含有量は、0.5質量%以下が好ましく、0.1質量%以下がより好ましく、0.05質量%以下が更に好ましく、アニオン界面活性剤を実質的に含有しないことがより更に好ましい。
[Anionic Surfactants]
Since the treatment agent of the present invention contains the cationic surfactants of components (A) and (B), if an excessive amount of anionic surfactant is added, the cationic surfactant and the anionic surfactant may form aggregates. Therefore, the content of the anionic surfactant in the treatment agent is preferably 0.5 mass% or less, more preferably 0.1 mass% or less, even more preferably 0.05 mass% or less, and even more preferably substantially free of anionic surfactant.
 〔水〕
 本発明の処理剤は、媒体として水を含有する。水は、成分(A)~(E)及びその他の成分の残量となる。
〔water〕
The treatment agent of the present invention contains water as a medium. The water constitutes the balance of components (A) to (E) and other components.
 〔その他の任意成分〕
 本発明の処理剤には、更に、毛髪化粧料又は頭飾製品用繊維処理剤に一般に使用されるその他の成分を、目的に応じて配合することができる。例えば、環状シリコーン、ジメチコノール、ポリエーテル変性シリコーン、ポリグリシドール変性シリコーン、メチルフェニルポリシロキサン、脂肪酸変性シリコーン、アルコール変性シリコーン、アルコキシ変性シリコーン、エポキシ変性シリコーン、フッ素変性シリコーン、アルキル変性シリコーン等の成分(D)及び(E)以外のシリコーン類;カチオン化セルロース、ヒドロキシアルキルセルロース、高重合ポリエチレンオキサイド等の高分子化合物;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ソルビタン脂肪酸エステル、グリセリンモノ脂肪酸エステル、ポリグリセリン脂肪酸エステル、ポリオキシエチレン硬化ヒマシ油、ショ糖脂肪酸エステル、ポリグリセリンアルキルエーテル、脂肪酸アルカノールアミド、アルキルグリコシド等の非イオン界面活性剤;スクワレン、スクワラン、流動パラフィン、流動イソパラフィン、シクロパラフィン等の炭化水素;ヒマシ油、カカオ油、ミンク油、アボカド油、オリーブ油等のグリセリド類;ミツロウ、鯨ロウ、ラノリン、カルナウバロウ等のロウ類;パルミチン酸イソプロピル、ミリスチン酸イソプロピル、ミリスチン酸オクチルドデシル、ラウリン酸ヘキシル、乳酸セチル、モノステアリン酸プロピレングリコール、オレイン酸オレイル、2-エチルヘキサン酸ヘキサデシル、イソノナン酸イソノニル、イソノナン酸トリデシル等のエステル;カプリン酸、ラウリン酸、ミリスチン酸、パルミチン酸、ステアリン酸、ベヘニン酸、オレイン酸、ヤシ油脂肪酸、ラノリン脂肪酸、イソステアリン酸、イソパルミチン酸等の高級脂肪酸;イソステアリルグリセリルエーテル、ポリオキシプロピレンブチルエーテルなどの油剤;エタノール、1-プロパノール、2-プロパノール、ブタノール、エチレングリコール、プロピレングリコール、メチルカルビトール、エチルカルビトール、プロピルカルビトール、ブチルカルビトール、トリエチレングリコールモノエチルエーテル、トリエチレングリコールモノブチルエーテル、グリセリン等のアルコール類;ジンクピリチオン、塩化ベンザルコニウム等の抗フケ剤;pH調整剤;ビタミン剤;殺菌剤;抗炎症剤;防腐剤;キレート剤;パンテノール等の保湿剤;染料、顔料等の着色剤;ユーカリの極性溶媒抽出物、真珠層を有する貝殻又は真珠から得られる蛋白質又はその加水分解物、シルクから得られる蛋白質又はその加水分解物、マメ科植物の種子から得られる蛋白含有抽出物、オタネニンジン抽出物、米胚芽抽出物、ヒバマタ抽出物、ツバキ抽出物、アロエ抽出物、月桃葉抽出物、クロレラ抽出物等のエキス類;雲母チタン等のパール粉体;メントール等の清涼剤:香料;色素;紫外線吸収剤;酸化防止剤;その他エンサイクロペディア・オブ・シャンプー・イングリーディエンツ(ENCYCLOPEDIA OF SHAMPOO INGREDIENTS (MICELLE PRESS))に記載されている成分等が挙げられる。
[Other optional ingredients]
The treatment agent of the present invention may further contain other components generally used in hair cosmetics or fiber treatment agents for head accessories, depending on the purpose. For example, silicones other than components (D) and (E), such as cyclic silicone, dimethiconol, polyether-modified silicone, polyglycidol-modified silicone, methylphenylpolysiloxane, fatty acid-modified silicone, alcohol-modified silicone, alkoxy-modified silicone, epoxy-modified silicone, fluorine-modified silicone, and alkyl-modified silicone; polymeric compounds, such as cationic cellulose, hydroxyalkyl cellulose, and highly polymerized polyethylene oxide; polyoxyethylene alkyl ether, polyoxyethylene sorbitan fatty acid ester, glycerin mono fatty acid ester, polyglycerin fatty acid ester, polyoxyethylene hydrogenated castor oil, and sucrose. Nonionic surfactants such as fatty acid esters, polyglycerol alkyl ethers, fatty acid alkanolamides, and alkyl glycosides; hydrocarbons such as squalene, squalane, liquid paraffin, liquid isoparaffin, and cycloparaffin; glycerides such as castor oil, cocoa oil, mink oil, avocado oil, and olive oil; waxes such as beeswax, spermaceti, lanolin, and carnauba wax; esters such as isopropyl palmitate, isopropyl myristate, octyldodecyl myristate, hexyl laurate, cetyl lactate, propylene glycol monostearate, oleyl oleate, hexadecyl 2-ethylhexanoate, isononyl isononanoate, and tridecyl isononanoate. higher fatty acids such as capric acid, lauric acid, myristic acid, palmitic acid, stearic acid, behenic acid, oleic acid, coconut oil fatty acid, lanolin fatty acid, isostearic acid, and isopalmitic acid; oils such as isostearyl glyceryl ether and polyoxypropylene butyl ether; alcohols such as ethanol, 1-propanol, 2-propanol, butanol, ethylene glycol, propylene glycol, methyl carbitol, ethyl carbitol, propyl carbitol, butyl carbitol, triethylene glycol monoethyl ether, triethylene glycol monobutyl ether, and glycerin; antibacterial agents such as zinc pyrithione and benzalkonium chloride. Examples of ingredients that may be used include dandruff agents; pH adjusters; vitamins; disinfectants; anti-inflammatory agents; preservatives; chelating agents; moisturizers such as panthenol; colorants such as dyes and pigments; extracts such as polar solvent extracts of eucalyptus, proteins or hydrolysates thereof obtained from shells or pearls having nacre, proteins or hydrolysates thereof obtained from silk, protein-containing extracts obtained from the seeds of legumes, ginseng extract, rice germ extract, hibamata extract, camellia extract, aloe extract, shell ginger leaf extract, and chlorella extract; pearl powders such as titanium mica; cooling agents such as menthol; fragrances; pigments; ultraviolet absorbers; antioxidants; and other ingredients listed in the Encyclopedia of Shampoo Ingredients (MICELLE PRESS).
 〔pH〕
 本発明の処理剤のpHは、2.0以上が好ましく、更には2.5以上が好ましく、7.5以下が好ましく、更には6.5以下、より更には5.5以下が好ましい。そして、本発明の処理剤のpHの具体的範囲は、2.0~7.5、更には2.5~6.5、より更には2.5~5.5が好ましい。なお、本発明において、処理剤のpHは、水で20質量倍希釈したときの25℃における値をいう。上記pHは、pHメーターを用いて測定することができる。
[pH]
The pH of the treatment agent of the present invention is preferably 2.0 or more, more preferably 2.5 or more, and is preferably 7.5 or less, more preferably 6.5 or less, and even more preferably 5.5 or less. The specific range of the pH of the treatment agent of the present invention is preferably 2.0 to 7.5, more preferably 2.5 to 6.5, and even more preferably 2.5 to 5.5. In the present invention, the pH of the treatment agent refers to the value at 25°C when diluted 20 times by mass with water. The above pH can be measured using a pH meter.
 〔粘度〕
 本発明の処理剤の粘度は、濡れた状態でのきしみ感や絡まりのなさを持続させる観点から、500mPa・s以上10万mPa・s以下の範囲が好ましい。毛髪又は頭飾製品用繊維への塗布性、手や髪、頭飾製品用繊維からの垂れ落ち防止の観点から、好ましくは1,000mPa・s以上、より好ましくは5,000mPa・s以上、更に好ましくは10,000mPa・s以上である。また、本発明の処理剤の粘度は、髪又は頭飾製品用繊維への塗り伸ばしやすさの観点から、好ましくは50,000mPa・s以下、より好ましくは40,000mPa・s以下、更に好ましくは30,000mPa・s以下である。そして、本発明の処理剤の粘度の具体的範囲は、好ましくは500~10万mPa・s、より好ましくは1,000~50,000mPa・s、更に好ましくは5,000~40,000mPa・s、より更に好ましくは10,000~30,000mPa・sである。ここで、本発明において粘度は、30℃においてB型粘度計又はBM型粘度計を用いて測定する。また、測定時に使用するローターや回転数は、処理剤の粘度に応じてマニュアル等に従い、適切な条件を選択する。
〔viscosity〕
The viscosity of the treatment agent of the present invention is preferably in the range of 500 mPa·s to 100,000 mPa·s from the viewpoint of maintaining the absence of squeaky feeling and tangling in a wet state. From the viewpoint of applicability to hair or fibers for head ornament products and prevention of dripping from hands, hair, or fibers for head ornament products, it is preferably 1,000 mPa·s or more, more preferably 5,000 mPa·s or more, and even more preferably 10,000 mPa·s or more. In addition, from the viewpoint of ease of spreading on hair or fibers for head ornament products, the viscosity of the treatment agent of the present invention is preferably 50,000 mPa·s or less, more preferably 40,000 mPa·s or less, and even more preferably 30,000 mPa·s or less. The specific range of the viscosity of the treatment agent of the present invention is preferably 500 to 100,000 mPa·s, more preferably 1,000 to 50,000 mPa·s, even more preferably 5,000 to 40,000 mPa·s, and even more preferably 10,000 to 30,000 mPa·s. Here, in the present invention, the viscosity is measured at 30° C. using a Brookfield viscometer or a BM type viscometer. In addition, the rotor and rotation speed used during measurement are selected according to the viscosity of the treatment agent, and appropriate conditions are selected in accordance with the manual or the like.
 〔処理剤の形態、毛髪又は頭飾製品用繊維の処理方法〕
 本発明の処理剤は、プレシャンプートリートメント、シャンプー、ヘアリンス、ヘアコンディショナー、ヘアトリートメント、ヘアパック、アフターシャンプートリートメント等のインバス剤(毛髪又は頭飾製品用繊維に適用した後に洗い流すタイプ);ノンエアゾールフォーム、エアゾールフォーム、ヘアジェル、ヘアムース、ヘアミスト、ヘアローション、ヘアオイル、スタイリング剤等のアウトバス剤(毛髪又は頭飾製品用繊維に適用した後に洗い流さないタイプ)などに好適に用いることができる。なかでも、インバス剤(毛髪又は頭飾製品用繊維に適用した後に洗い流すタイプ)が好ましい。処理対象の毛髪又は頭飾製品用繊維は、特に限定されるものではないが、ヘアカラー等の染色処理後の毛髪又は頭飾製品用繊維に対して好適に使用することができる。
[Form of treatment agent, treatment method for hair or fibers for head accessories]
The treatment agent of the present invention can be suitably used as an in-bath agent (a type that is applied to hair or fibers for head ornament products and then washed off) such as a pre-shampoo treatment, shampoo, hair rinse, hair conditioner, hair treatment, hair pack, or after-shampoo treatment; or an out-bath agent (a type that is applied to hair or fibers for head ornament products and then not washed off) such as a non-aerosol foam, aerosol foam, hair gel, hair mousse, hair mist, hair lotion, hair oil, or styling agent. Among these, an in-bath agent (a type that is applied to hair or fibers for head ornament products and then washed off) is preferred. The hair or fibers for head ornament products to be treated is not particularly limited, but the agent can be suitably used for hair or fibers for head ornament products after dyeing treatment such as hair coloring.
 本発明の処理剤がインバス剤の場合、毛髪又は頭飾製品用繊維のコンディショニング処理を行うには、本発明の処理剤を毛髪又は頭飾製品用繊維に塗布した後、水で洗い流せばよい。これにより、処理後の毛髪又は頭飾製品用繊維を繰り返し洗浄した後においても、濡れた状態でのきしみ感や絡まりのなさを持続させることができる。 When the treatment agent of the present invention is an in-bath agent, conditioning of hair or fibers for head accessories can be performed by applying the treatment agent of the present invention to the hair or fibers for head accessories and then rinsing it off with water. This allows the treated hair or fibers for head accessories to maintain their lack of squeaky feeling and tangles in a wet state even after repeated washing.
 以上、述べた実施形態に関し、以下に本発明の好ましい態様を更に開示する。 With regard to the above-described embodiment, further preferred aspects of the present invention are disclosed below.
 <1>次の成分(A)~(C)、並びに成分(D)及び成分(E)から選択される1種以上を含有し、成分(D)及び成分(E)の合計含有量が1質量%以上15質量%以下である、毛髪処理剤又は頭飾製品用繊維処理剤。
 (A) エーテルアミン又はその塩、アミドアミン又はその塩、及び炭素数18以上のアルキル基を有するモノ長鎖アルキル第4級アンモニウム塩からなる群より選ばれる1種以上のカチオン界面活性剤
 (B) 炭素数16以下のアルキル基を有するモノ長鎖アルキル第4級アンモニウム塩 0.1質量%以上2.8質量%以下
 (C) 高級アルコール 1質量%以上15質量%以下
 (D) アミノ変性シリコーン及びアミノポリエーテル変性シリコーンからなる群より選ばれる1種以上の変性シリコーン
 (E) ジメチコン
<1> A hair treatment agent or a fiber treatment agent for a head accessory product, comprising one or more components selected from the following components (A) to (C), as well as components (D) and (E), wherein the total content of components (D) and (E) is 1% by mass or more and 15% by mass or less.
(A) One or more cationic surfactants selected from the group consisting of ether amines or their salts, amido amines or their salts, and mono-long-chain alkyl quaternary ammonium salts having an alkyl group with 18 or more carbon atoms. (B) Mono-long-chain alkyl quaternary ammonium salts having an alkyl group with 16 or less carbon atoms, 0.1% by mass or more and 2.8% by mass or less. (C) Higher alcohol, 1% by mass or more and 15% by mass or less. (D) One or more modified silicones selected from the group consisting of amino-modified silicones and aminopolyether-modified silicones. (E) Dimethicone.
 <2>エーテルアミンが、好ましくは下記一般式(1)で表される化合物である、<1>に記載の毛髪処理剤又は頭飾製品用繊維処理剤。 <2> The hair treatment agent or fiber treatment agent for head accessories according to <1>, wherein the etheramine is preferably a compound represented by the following general formula (1):
Figure JPOXMLDOC01-appb-C000008
Figure JPOXMLDOC01-appb-C000008
 〔式中、R1は、炭素数6~24の直鎖又は分岐鎖のアルキル基又はアルケニル基を示し、R2及びR3は、同一でも異なってもよく、炭素数1~6のアルキル基又は-(A1O)H(A1は炭素数2~4のアルキレン基を示し、mは1~6の数を示し、m個のA1Oは同一でも異なってもよく、その配列は任意である)を示す。Yは水素原子又は水酸基を示す。〕 [In the formula, R 1 represents a linear or branched alkyl or alkenyl group having 6 to 24 carbon atoms, R 2 and R 3 may be the same or different, and represent an alkyl group having 1 to 6 carbon atoms or -(A 1 O) m H (A 1 represents an alkylene group having 2 to 4 carbon atoms, m represents a number from 1 to 6, m A 1 Os may be the same or different, and the arrangement is arbitrary), and Y represents a hydrogen atom or a hydroxyl group.]
 <3>エーテルアミン又はその塩が、好ましくはN,N-ジメチル-3-ヘキサデシルオキシプロピルアミン又はその塩、N,N-ジメチル-3-オクタデシルオキシプロピルアミン又はその塩、ヘキサデシルオキシ(2-ヒドロキシプロピル)ジメチルアミン又はその塩、及びオクタデシルオキシ(2-ヒドロキシプロピル)ジメチルアミン又はその塩から選ばれる1種以上、より好ましくはN,N-ジメチル-3-オクタデシルオキシプロピルアミン又はその塩、及びオクタデシルオキシ(2-ヒドロキシプロピル)ジメチルアミン又はその塩から選ばれる1種以上である、<1>又は<2>に記載の毛髪処理剤又は頭飾製品用繊維処理剤。 <3> The hair treatment agent or fiber treatment agent for head accessories according to <1> or <2>, wherein the etheramine or its salt is preferably one or more selected from N,N-dimethyl-3-hexadecyloxypropylamine or its salt, N,N-dimethyl-3-octadecyloxypropylamine or its salt, hexadecyloxy(2-hydroxypropyl)dimethylamine or its salt, and octadecyloxy(2-hydroxypropyl)dimethylamine or its salt, more preferably one or more selected from N,N-dimethyl-3-octadecyloxypropylamine or its salt, and octadecyloxy(2-hydroxypropyl)dimethylamine or its salt.
 <4>アミドアミンが、好ましくは下記一般式(2)で表される化合物である、<1>~<3>のいずれか1項に記載の毛髪処理剤又は頭飾製品用繊維処理剤。 <4> A hair treatment agent or a fiber treatment agent for head accessories according to any one of <1> to <3>, wherein the amidoamine is preferably a compound represented by the following general formula (2):
Figure JPOXMLDOC01-appb-C000009
Figure JPOXMLDOC01-appb-C000009
 〔式中、R4は炭素数17~21の直鎖又は分岐鎖のアルキル基を示し、2個のR5は同一の炭素数1~4のアルキル基を示し、nは2~4の数を示す。〕 [In the formula, R 4 represents a linear or branched alkyl group having 17 to 21 carbon atoms, two R 5 represent the same alkyl group having 1 to 4 carbon atoms, and n represents a number from 2 to 4.]
 <5>アミドアミン又はその塩が、好ましくはステアリン酸ジメチルアミノエチルアミド又はその塩、ステアリン酸ジメチルアミノプロピルアミド又はその塩、ステアリン酸ジエチルアミノエチルアミド又はその塩、ステアリン酸ジエチルアミノプロピルアミド又はその塩、ステアリン酸ジプロピルアミノエチルアミド又はその塩、ステアリン酸ジプロピルアミノプロピルアミド又はその塩、ベヘン酸ジメチルアミノプロピルアミド又はその塩、及びベヘン酸ジエチルアミノプロピルアミド又はその塩から選ばれる1種以上、より好ましくはステアリン酸ジメチルアミノプロピルアミド又はその塩、ステアリン酸ジエチルアミノエチルアミド又はその塩、ベヘン酸ジメチルアミノプロピルアミド又はその塩、及びベヘン酸ジエチルアミノプロピルアミド又はその塩であるから選ばれる1種以上である、<1>~<4>のいずれか1項に記載の毛髪処理剤又は頭飾製品用繊維処理剤。 <5> The hair treatment agent or fiber treatment agent for head accessories according to any one of <1> to <4>, wherein the amidoamine or its salt is preferably one or more selected from dimethylaminoethylamide stearate or its salt, dimethylaminopropylamide stearate or its salt, diethylaminoethylamide stearate or its salt, diethylaminopropylamide stearate or its salt, dipropylaminoethylamide stearate or its salt, dipropylaminopropylamide stearate or its salt, dimethylaminopropylamide behenate or its salt, and diethylaminopropylamide behenate or its salt, more preferably one or more selected from dimethylaminopropylamide stearate or its salt, diethylaminoethylamide stearate or its salt, dimethylaminopropylamide behenate or its salt, and diethylaminopropylamide behenate or its salt.
 <6>炭素数18以上のアルキル基を有するモノ長鎖アルキル第4級アンモニウム塩が、好ましくは下記一般式(3)で表される化合物である、<1>~<5>のいずれか1項に記載の毛髪処理剤又は頭飾製品用繊維処理剤。 <6> A hair treatment agent or a fiber treatment agent for head accessories according to any one of <1> to <5>, wherein the mono-long-chain alkyl quaternary ammonium salt having an alkyl group having 18 or more carbon atoms is preferably a compound represented by the following general formula (3):
Figure JPOXMLDOC01-appb-C000010
Figure JPOXMLDOC01-appb-C000010
 〔式中、R6は炭素数18~22の飽和若しくは不飽和の直鎖若しくは分岐鎖のアルキル基、R10-CO-NH-(CH2)a-又はR10-CO-O-(CH2)a-(R10は炭素数18~21の飽和又は不飽和の直鎖又は分岐鎖のアルキル鎖を示し、aは1~4の整数を示す)を示し、R7、R8及びR9は独立して、炭素数1~4のアルキル基、炭素数1~4のヒドロキシルアルキル基を示し、X-は塩化物イオン、臭化物イオン、メトサルフェートイオン又はエトサルフェートイオンを示す。〕 [In the formula, R 6 represents a saturated or unsaturated, linear or branched alkyl group having 18 to 22 carbon atoms, R 10 -CO-NH-(CH 2 ) a - or R 10 -CO-O-(CH 2 ) a - (R 10 represents a saturated or unsaturated, linear or branched alkyl chain having 18 to 21 carbon atoms, and a represents an integer of 1 to 4), R 7 , R 8 and R 9 independently represent an alkyl group having 1 to 4 carbon atoms or a hydroxylalkyl group having 1 to 4 carbon atoms, and X - represents a chloride ion, a bromide ion, a methosulfate ion or an ethosulfate ion.]
 <7>炭素数18以上のアルキル基を有するモノ長鎖アルキル第4級アンモニウム塩が、好ましくはステアルトリモニウムクロリド、ステアルトリモニウムブロミド、ステアルトリモニウムメトサルフェート、ベヘントリモニウムクロリド、ベヘントリモニウムメトサルフェート、ベヘナミドプロピルトリモニウムクロリド、ベヘナミドプロピルトリモニウムメトサルフェート、ベヘナミドプロピルエチルジモニウムエトサルフェート、及びベヘナミドプロピルPGジモニウムクロリドから選ばれる1種以上である、<1>~<6>のいずれか1項に記載の毛髪処理剤又は頭飾製品用繊維処理剤。 <7> A hair treatment agent or a fiber treatment agent for head accessories according to any one of <1> to <6>, wherein the mono long-chain alkyl quaternary ammonium salt having an alkyl group having 18 or more carbon atoms is preferably one or more selected from steartrimonium chloride, steartrimonium bromide, steartrimonium methosulfate, behentrimonium chloride, behentrimonium methosulfate, behenamidopropyltrimonium chloride, behenamidopropyltrimonium methosulfate, behenamidopropyl ethyldimonium ethosulfate, and behenamidopropyl PG-dimonium chloride.
 <8>成分(A)の含有量が、好ましくは1~10質量%、より好ましくは1.5~5質量%、更に好ましくは2~3質量%である、<1>~<7>のいずれか1項に記載の毛髪処理剤又は頭飾製品用繊維処理剤。 <8> A hair treatment agent or a fiber treatment agent for head accessories according to any one of <1> to <7>, in which the content of component (A) is preferably 1 to 10 mass%, more preferably 1.5 to 5 mass%, and even more preferably 2 to 3 mass%.
 <9>成分(B)のモノ長鎖アルキル第4級アンモニウム塩のアルキル基が、好ましくは炭素数12以上16以下であるもの、より好ましくは炭素数14以上16以下であるもの、更に好ましくは炭素数16であるものである、<1>~<8>のいずれか1項に記載の毛髪処理剤又は頭飾製品用繊維処理剤。 <9> The hair treatment agent or fiber treatment agent for head accessories according to any one of <1> to <8>, wherein the alkyl group of the mono-long-chain alkyl quaternary ammonium salt of component (B) preferably has 12 to 16 carbon atoms, more preferably has 14 to 16 carbon atoms, and even more preferably has 16 carbon atoms.
 <10>成分(B)が、好ましくはセトリモニウムクロリド、セトリモニウムブロミド、及びセトリモニウムメトサルフェートから選ばれる1種以上、より好ましくはセトリモニウムクロリドである、<1>~<9>のいずれか1項に記載の毛髪処理剤又は頭飾製品用繊維処理剤。 <10> A hair treatment agent or a fiber treatment agent for head accessories according to any one of <1> to <9>, wherein component (B) is preferably one or more selected from cetrimonium chloride, cetrimonium bromide, and cetrimonium methosulfate, more preferably cetrimonium chloride.
 <11>成分(B)の含有量が、好ましくは0.2~2.5質量%以上、より好ましくは0.3~2.3質量%である、<1>~<10>のいずれか1項に記載の毛髪処理剤又は頭飾製品用繊維処理剤。 <11> A hair treatment agent or a fiber treatment agent for head accessories according to any one of <1> to <10>, wherein the content of component (B) is preferably 0.2 to 2.5 mass% or more, more preferably 0.3 to 2.3 mass%.
 <12>成分(A)及び(B)の合計含有量が、好ましくは1.1~12.8質量%、より好ましくは1.7~7.5質量%、更に好ましくは2.3~5.3質量%である、<1>~<11>のいずれか1項に記載の毛髪処理剤又は頭飾製品用繊維処理剤。 <12> A hair treatment agent or a fiber treatment agent for head accessories according to any one of <1> to <11>, wherein the total content of components (A) and (B) is preferably 1.1 to 12.8% by mass, more preferably 1.7 to 7.5% by mass, and even more preferably 2.3 to 5.3% by mass.
 <13>成分(A)に対する成分(B)の質量比(B)/(A)が、好ましくは0.01~1.2、より好ましくは0.05~1.1、更に好ましくは0.1~1.0、より更に好ましくは0.1~0.5である、<1>~<12>のいずれか1項に記載の毛髪処理剤又は頭飾製品用繊維処理剤。 <13> The hair treatment agent or fiber treatment agent for head accessories according to any one of <1> to <12>, wherein the mass ratio (B)/(A) of component (B) to component (A) is preferably 0.01 to 1.2, more preferably 0.05 to 1.1, even more preferably 0.1 to 1.0, and even more preferably 0.1 to 0.5.
 <14>成分(C)の高級アルコールの炭素数が、好ましくは12~22、より好ましくは14~20、更に好ましくは16~18である、<1>~<13>のいずれか1項に記載の毛髪処理剤又は頭飾製品用繊維処理剤。 <14> The hair treatment agent or fiber treatment agent for head accessories according to any one of <1> to <13>, wherein the carbon number of the higher alcohol of component (C) is preferably 12 to 22, more preferably 14 to 20, and even more preferably 16 to 18.
 <15>成分(C)が、好ましくはラウリルアルコール、ミリスチルアルコール、セチルアルコール、ステアリルアルコール、アラキルアルコール、ヘキシルデカノール、イソステアリルアルコール、オレイルアルコール、及び2-オクチルドデカノールから選ばれる1種以上、より好ましくはステアリルアルコール、セチルアルコール、及びミリスチルアルコールから選ばれる1種以上、より好ましくはステアリルアルコール、及びセチルアルコールから選ばれる1種以上、更に好ましくはステアリルアルコールである、<1>~<14>のいずれか1項に記載の毛髪処理剤又は頭飾製品用繊維処理剤。 <15> A hair treatment agent or a fiber treatment agent for head accessories according to any one of <1> to <14>, wherein component (C) is preferably at least one selected from lauryl alcohol, myristyl alcohol, cetyl alcohol, stearyl alcohol, arachyl alcohol, hexyldecanol, isostearyl alcohol, oleyl alcohol, and 2-octyldodecanol, more preferably at least one selected from stearyl alcohol, cetyl alcohol, and myristyl alcohol, more preferably at least one selected from stearyl alcohol and cetyl alcohol, and even more preferably stearyl alcohol.
 <16>成分(C)の含有量が、好ましくは3~12質量%、より好ましくは5~10質量%以上である、<1>~<15>のいずれか1項に記載の毛髪処理剤又は頭飾製品用繊維処理剤。 <16> A hair treatment agent or a fiber treatment agent for head accessories according to any one of <1> to <15>, in which the content of component (C) is preferably 3 to 12 mass%, more preferably 5 to 10 mass% or more.
 <17>成分(D)のアミノ変性シリコーンが、好ましくは下記一般式(4)で表される、<1>~<16>のいずれか1項に記載の毛髪処理剤又は頭飾製品用繊維処理剤。 <17> A hair treatment agent or a fiber treatment agent for head accessories according to any one of <1> to <16>, wherein the amino-modified silicone of component (D) is preferably represented by the following general formula (4):
Figure JPOXMLDOC01-appb-C000011
Figure JPOXMLDOC01-appb-C000011
 〔式中、R10はそれぞれ独立に、メチル基又はヒドロキシ基を示し、R11はそれぞれ独立に、炭素数1以上30以下のアルキル基、ヒドロキシ基、又はR12を示す。R12は-R13-Z1(R13は単結合、又は炭素数1以上20以下の2価の炭化水素基を示し、Z1は1~3級アミノ基含有基又はアンモニウム基含有基を示す)で表される1価の基を示す。aは0以上3000以下、bは1以上3000以下の数を示す。〕 [In the formula, R 10 each independently represents a methyl group or a hydroxy group, and R 11 each independently represents an alkyl group having 1 to 30 carbon atoms, a hydroxy group, or R 12. R 12 represents a monovalent group represented by -R 13 -Z 1 (R 13 represents a single bond or a divalent hydrocarbon group having 1 to 20 carbon atoms, and Z 1 represents a primary to tertiary amino group-containing group or an ammonium group-containing group). a represents a number of 0 to 3,000, and b represents a number of 1 to 3,000.]
 <18>一般式(4)で表されるアミノ変性シリコーンが、好ましくはアモジメチコン、アミノプロピルジメチコン、ビス(アミノプロピル)ジメチコン、及びビス(セテアリル)アモジメチコンからなる群より選ばれる1種以上、より好ましくは下記一般式(4a)~(4d)のいずれかで表される化合物であり、更に好ましくは下記一般式(4a)で表されるアミノ変性シリコーン(アモジメチコン)である、<17>に記載の毛髪処理剤又は頭飾製品用繊維処理剤。 <18> The hair treatment agent or fiber treatment agent for head accessories according to <17>, wherein the amino-modified silicone represented by the general formula (4) is preferably one or more selected from the group consisting of amodimethicone, aminopropyl dimethicone, bis(aminopropyl) dimethicone, and bis(cetearyl) amodimethicone, more preferably a compound represented by any one of the following general formulas (4a) to (4d), and even more preferably an amino-modified silicone (amodimethicone) represented by the following general formula (4a).
Figure JPOXMLDOC01-appb-C000012
Figure JPOXMLDOC01-appb-C000012
 〔式中、a、b、c及びR13は、前記と同じ意味を示す。〕 (In the formula, a, b, c and R 13 have the same meanings as defined above.)
 <19>成分(D)のアミノ変性シリコーンの25℃における動粘度の具体的範囲が、好ましくは20~10,000mm2/s、より好ましくは100~5,000mm2/s、更に好ましくは500~2,000mm2/sである、<1>~<18>のいずれか1項に記載の毛髪処理剤又は頭飾製品用繊維処理剤。 <19> The hair treatment agent or fiber treatment agent for head ornament products according to any one of <1> to <18>, wherein the specific range of the kinetic viscosity of the amino-modified silicone of component (D) at 25°C is preferably 20 to 10,000 mm2/s, more preferably 100 to 5,000 mm2 /s, and even more preferably 500 to 2,000 mm2 /s.
 <20>成分(D)のアミノポリエーテル変性シリコーンが、好ましくは下記一般式(5)で表される、<1>~<19>のいずれか1項に記載の毛髪処理剤又は頭飾製品用繊維処理剤。 <20> A hair treatment agent or a fiber treatment agent for head accessories according to any one of <1> to <19>, wherein the amino polyether-modified silicone of component (D) is preferably represented by the following general formula (5):
Figure JPOXMLDOC01-appb-C000013
Figure JPOXMLDOC01-appb-C000013
 〔式(5)中、R17は水素原子又は炭素数1以上6以下の1価の炭化水素基を示す。R18はR17又はEを示す。Eは-R19-Z2(R19は単結合、又は炭素数1以上20以下の2価の炭化水素基を示し、Z2は1~3級アミノ基含有基又はアンモニウム基含有基を示す)で表される1価の基を示す。Wは炭素数1以上6以下の2価の飽和炭化水素基を示す。
 dは2以上の数、eは1以上の数、fは2以上100以下の数、gは1以上の数を示す。xは2以上10以下の数を示す。括弧内の構造単位同士の結合順序は問わず、結合形態はブロック状でもランダム状でもよい。f個のCx2xOは同一でも異なっていてもよい。また、複数個のR17、R18、E及びWは同一でも異なっていてもよい。〕
[In formula (5), R 17 represents a hydrogen atom or a monovalent hydrocarbon group having 1 to 6 carbon atoms. R 18 represents R 17 or E. E represents a monovalent group represented by -R 19 -Z 2 (R 19 represents a single bond or a divalent hydrocarbon group having 1 to 20 carbon atoms, and Z 2 represents a primary to tertiary amino group-containing group or an ammonium group-containing group). W represents a divalent saturated hydrocarbon group having 1 to 6 carbon atoms.
d is a number of 2 or more, e is a number of 1 or more, f is a number of 2 or more and 100 or less, and g is a number of 1 or more. x is a number of 2 or more and 10 or less. The structural units in the parentheses may be bonded in any order, and may be bonded in a block or random form. f C x H 2x O may be the same or different. In addition, multiple R 17 , R 18 , E, and W may be the same or different.
 <21>成分(D)のアミノポリエーテル変性シリコーンが、より好ましくは下記一般式(5a)で表される、<20>に記載の毛髪処理剤又は頭飾製品用繊維処理剤。 <21> The hair treatment agent or fiber treatment agent for head accessories according to <20>, wherein the amino polyether-modified silicone of component (D) is more preferably represented by the following general formula (5a):
Figure JPOXMLDOC01-appb-C000014
Figure JPOXMLDOC01-appb-C000014
 〔式(5a)中、d~gは前記と同じ意味を示す。〕 [In formula (5a), d to g have the same meanings as above.]
 <22>成分(D)のアミノポリエーテル変性シリコーンの25℃における動粘度が、好ましくは5,000~200,000mm2/s、より好ましくは20,000~150,000mm2/s、更に好ましくは40,000~100,000mm2/sである、<1>~<21>のいずれか1項に記載の毛髪処理剤又は頭飾製品用繊維処理剤。 <22> The hair treatment agent or fiber treatment agent for head accessories according to any one of <1> to <21>, wherein the amino polyether-modified silicone of component (D) has a kinetic viscosity at 25°C of preferably 5,000 to 200,000 mm2 /s, more preferably 20,000 to 150,000 mm2 /s, and even more preferably 40,000 to 100,000 mm2 /s.
 <23>成分(D)の含有量が、好ましくは0.1~10質量%、より好ましくは0.4~7質量%、更に好ましくは0.8~5質量%である、<1>~<22>のいずれか1項に記載の毛髪処理剤又は頭飾製品用繊維処理剤。 <23> The hair treatment agent or fiber treatment agent for head accessories according to any one of <1> to <22>, wherein the content of component (D) is preferably 0.1 to 10 mass%, more preferably 0.4 to 7 mass%, and even more preferably 0.8 to 5 mass%.
 <24>成分(E)のジメチコンの25℃における動粘度が、好ましくは500~100万mm2/s、より好ましくは1,000~50万mm2/s、更に好ましくは5,000~30万mm2/s、より更に好ましくは1万~20万mm2/s、より更に好ましくは3万~20万mm2/s、より更に好ましくは5万~20万mm2/sである、<1>~<23>のいずれか1項に記載の毛髪処理剤又は頭飾製品用繊維処理剤。 <24> A hair treatment agent or a fiber treatment agent for head ornament products according to any one of <1> to <23>, wherein the kinetic viscosity of the dimethicone component (E) at 25°C is preferably 500 to 1,000,000 mm2 /s, more preferably 1,000 to 500,000 mm2 /s, even more preferably 5,000 to 300,000 mm2 /s, still more preferably 10,000 to 200,000 mm2 /s, still more preferably 30,000 to 200,000 mm2 /s, and even more preferably 50,000 to 200,000 mm2/s.
 <25>成分(E)の含有量が、好ましくは0.1~10質量%、より好ましくは1~8質量%、更に好ましくは2~6質量%である、<1>~<24>のいずれか1項に記載の毛髪処理剤又は頭飾製品用繊維処理剤。 <25> The hair treatment agent or fiber treatment agent for head accessories according to any one of <1> to <24>, wherein the content of component (E) is preferably 0.1 to 10 mass%, more preferably 1 to 8 mass%, and even more preferably 2 to 6 mass%.
 <26>好ましくは成分(D)及び成分(E)を含有する、<1>~<25>のいずれか1項に記載の毛髪処理剤又は頭飾製品用繊維処理剤。 <26> A hair treatment agent or a fiber treatment agent for a head accessory according to any one of <1> to <25>, preferably containing component (D) and component (E).
 <27>成分(D)及び(E)の合計含有量が、好ましくは1~12質量%、より好ましくは1~10質量%、更に好ましくは2~10質量%、より更に好ましくは3~10質量%、より更に好ましくは5~8質量%以上である、<1>~<26>のいずれか1項に記載の毛髪処理剤又は頭飾製品用繊維処理剤。 <27> The hair treatment agent or fiber treatment agent for head accessories according to any one of <1> to <26>, wherein the total content of components (D) and (E) is preferably 1 to 12 mass%, more preferably 1 to 10 mass%, even more preferably 2 to 10 mass%, even more preferably 3 to 10 mass%, and even more preferably 5 to 8 mass% or more.
 <28>成分(D)に対する成分(E)の質量比(E)/(D)が、好ましくは0.1~15、より好ましくは1~10、更に好ましくは2~7、より更に好ましくは3.5~7である、<1>~<27>のいずれか1項に記載の毛髪処理剤又は頭飾製品用繊維処理剤。 <28> The hair treatment agent or fiber treatment agent for head accessories according to any one of <1> to <27>, wherein the mass ratio (E)/(D) of component (E) to component (D) is preferably 0.1 to 15, more preferably 1 to 10, even more preferably 2 to 7, and even more preferably 3.5 to 7.
 <29>次の成分(A)~(C)、並びに成分(D)及び成分(E)から選択される1種以上を含有し、成分(D)及び成分(E)の合計含有量が1~10質量%である、毛髪処理剤又は頭飾製品用繊維処理剤。
 (A) 一般式(1)で表されるエーテルアミン又はその塩、一般式(2)で表されるアミドアミン又はその塩、及び一般式(3)で表される炭素数18以上のアルキル基を有するモノ長鎖アルキル第4級アンモニウム塩からなる群より選ばれる1種以上のカチオン界面活性剤 1~5質量%
<29> A hair treatment agent or a fiber treatment agent for a head accessory product, comprising one or more selected from the following components (A) to (C), as well as components (D) and (E), wherein the total content of components (D) and (E) is 1 to 10 mass%.
(A) 1 to 5% by mass of one or more cationic surfactants selected from the group consisting of ether amines represented by general formula (1) or salts thereof, amido amines represented by general formula (2) or salts thereof, and mono-long-chain alkyl quaternary ammonium salts having an alkyl group having 18 or more carbon atoms represented by general formula (3).
Figure JPOXMLDOC01-appb-C000015
Figure JPOXMLDOC01-appb-C000015
 〔式中、R1は、炭素数6~24の直鎖又は分岐鎖のアルキル基又はアルケニル基を示し、R2及びR3は、同一でも異なってもよく、炭素数1~6のアルキル基又は-(A1O)H(A1は炭素数2~4のアルキレン基を示し、mは1~6の数を示し、m個のA1Oは同一でも異なってもよく、その配列は任意である)を示す。Yは水素原子又は水酸基を示す。〕 [In the formula, R 1 represents a linear or branched alkyl or alkenyl group having 6 to 24 carbon atoms, R 2 and R 3 may be the same or different, and represent an alkyl group having 1 to 6 carbon atoms or -(A 1 O) m H (A 1 represents an alkylene group having 2 to 4 carbon atoms, m represents a number from 1 to 6, m A 1 Os may be the same or different, and the arrangement is arbitrary), and Y represents a hydrogen atom or a hydroxyl group.]
Figure JPOXMLDOC01-appb-C000016
Figure JPOXMLDOC01-appb-C000016
 〔式中、R4は炭素数17~21の直鎖又は分岐鎖のアルキル基を示し、2個のR5は同一の炭素数1~4のアルキル基を示し、nは2~4の数を示す。〕 [In the formula, R 4 represents a linear or branched alkyl group having 17 to 21 carbon atoms, two R 5 represent the same alkyl group having 1 to 4 carbon atoms, and n represents a number from 2 to 4.]
Figure JPOXMLDOC01-appb-C000017
Figure JPOXMLDOC01-appb-C000017
 〔式中、R6は炭素数18~22の飽和若しくは不飽和の直鎖若しくは分岐鎖のアルキル基、R10-CO-NH-(CH2)a-又はR10-CO-O-(CH2)a-(R10は炭素数18~21の飽和又は不飽和の直鎖又は分岐鎖のアルキル鎖を示し、aは1~4の整数を示す)を示し、R7、R8及びR9は独立して、炭素数1~4のアルキル基、炭素数1~4のヒドロキシルアルキル基を示し、X-は塩化物イオン、臭化物イオン、メトサルフェートイオン又はエトサルフェートイオンを示す。〕
 (B) 炭素数16のアルキル基を有するモノ長鎖アルキル第4級アンモニウム塩 0.1~2.5質量%
 (C) 炭素数12~22の直鎖又は分岐鎖の飽和脂肪族アルコール 5~10質量%
 (D) アミノ変性シリコーン及びアミノポリエーテル変性シリコーンからなる群より選ばれる1種以上の変性シリコーン
 (E) ジメチコン
[In the formula, R 6 represents a saturated or unsaturated, linear or branched alkyl group having 18 to 22 carbon atoms, R 10 -CO-NH-(CH 2 ) a - or R 10 -CO-O-(CH 2 ) a - (R 10 represents a saturated or unsaturated, linear or branched alkyl chain having 18 to 21 carbon atoms, and a represents an integer of 1 to 4), R 7 , R 8 and R 9 independently represent an alkyl group having 1 to 4 carbon atoms or a hydroxylalkyl group having 1 to 4 carbon atoms, and X - represents a chloride ion, a bromide ion, a methosulfate ion or an ethosulfate ion.]
(B) 0.1 to 2.5% by mass of mono-long chain alkyl quaternary ammonium salt having an alkyl group with 16 carbon atoms
(C) Linear or branched chain saturated aliphatic alcohols having 12 to 22 carbon atoms: 5 to 10% by mass
(D) One or more modified silicones selected from the group consisting of amino-modified silicones and aminopolyether-modified silicones. (E) Dimethicone.
 <30>次の成分(A)~(C)、並びに成分(D)及び成分(E)から選択される1種以上を含有し、成分(D)及び成分(E)の合計含有量が1~10質量%である、毛髪処理剤又は頭飾製品用繊維処理剤。
 (A) 一般式(1)で表されるエーテルアミン又はその塩からなる群より選ばれる1種以上のカチオン界面活性剤 1~5質量%
<30> A hair treatment agent or a fiber treatment agent for a head accessory product, comprising one or more selected from the following components (A) to (C), as well as components (D) and (E), wherein the total content of components (D) and (E) is 1 to 10 mass%.
(A) 1 to 5% by mass of one or more cationic surfactants selected from the group consisting of ether amines represented by general formula (1) or salts thereof
Figure JPOXMLDOC01-appb-C000018
Figure JPOXMLDOC01-appb-C000018
 〔式中、R1は、炭素数6~24の直鎖又は分岐鎖のアルキル基又はアルケニル基を示し、R2及びR3は、同一でも異なってもよく、炭素数1~6のアルキル基又は-(A1O)H(A1は炭素数2~4のアルキレン基を示し、mは1~6の数を示し、m個のA1Oは同一でも異なってもよく、その配列は任意である)を示す。Yは水素原子又は水酸基を示す。〕
 (B) 炭素数16のアルキル基を有するモノ長鎖アルキル第4級アンモニウム塩 0.1~2.5質量%
 (C) 炭素数12~22の直鎖又は分岐鎖の飽和脂肪族アルコール 5~10質量%
 (D) 一般式(1a)~(1d)のいずれかで表されるアミノ変性シリコーンからなる群より選ばれる1種以上の変性シリコーン
 (E) 25℃における動粘度が5,000~20万mm2/sであるジメチコン
[In the formula, R 1 represents a linear or branched alkyl or alkenyl group having 6 to 24 carbon atoms, R 2 and R 3 may be the same or different, and represent an alkyl group having 1 to 6 carbon atoms or -(A 1 O) m H (A 1 represents an alkylene group having 2 to 4 carbon atoms, m represents a number from 1 to 6, m A 1 Os may be the same or different, and the arrangement is arbitrary), and Y represents a hydrogen atom or a hydroxyl group.]
(B) 0.1 to 2.5% by mass of mono-long chain alkyl quaternary ammonium salt having an alkyl group with 16 carbon atoms
(C) Linear or branched chain saturated aliphatic alcohols having 12 to 22 carbon atoms: 5 to 10% by mass
(D) One or more modified silicones selected from the group consisting of amino-modified silicones represented by any one of the general formulas (1a) to (1d): (E) Dimethicone having a kinetic viscosity at 25°C of 5,000 to 200,000 mm2 /s.
 <31>成分(D)に対する成分(E)の質量比(E)/(D)が、3.5以上7以下である、<29>又は<30>に記載の毛髪処理剤又は頭飾製品用繊維処理剤。 <31> A hair treatment agent or a fiber treatment agent for head accessories according to <29> or <30>, in which the mass ratio (E)/(D) of component (E) to component (D) is 3.5 or more and 7 or less.
 <32>成分(A)に対する成分(B)の質量比(B)/(A)が、0.1~0.17及び0.1~0.5のいずれかの範囲である、<29>~<31>のいずれか1項に記載の毛髪処理剤又は頭飾製品用繊維処理剤。 <32> A hair treatment agent or a fiber treatment agent for a head accessory according to any one of <29> to <31>, wherein the mass ratio (B)/(A) of component (B) to component (A) is in the range of either 0.1 to 0.17 or 0.1 to 0.5.
 <33>好ましくは、更に有機酸又はその塩を含有し、有機酸が、好ましくはカルボン酸系化合物、より好ましくは分子量が500以下、より好ましくは200以下の化合物、更に好ましくは脂肪族モノカルボン酸、芳香族モノカルボン酸、脂肪族ジカルボン酸、芳香族ジカルボン酸、ポリカルボン酸、ヒドロキシカルボン酸、及び酸性アミノ酸から選ばれる1種以上である、<1>~<32>のいずれか1項に記載の毛髪処理剤又は頭飾製品用繊維処理剤。 <33> The hair treatment agent or fiber treatment agent for head accessories according to any one of <1> to <32>, further comprising an organic acid or a salt thereof, the organic acid being preferably a carboxylic acid compound, more preferably a compound having a molecular weight of 500 or less, more preferably 200 or less, and even more preferably one or more selected from aliphatic monocarboxylic acids, aromatic monocarboxylic acids, aliphatic dicarboxylic acids, aromatic dicarboxylic acids, polycarboxylic acids, hydroxycarboxylic acids, and acidic amino acids.
 <34>有機酸が、好ましくは酢酸、プロピオン酸、ブタン酸、安息香酸、マロン酸、コハク酸、グルタル酸、アジピン酸、マレイン酸、フマル酸、フタル酸、イソフタル酸、ポリグルタミン酸、乳酸、リンゴ酸、グリコール酸、ヒドロキシアクリル酸、グリセリン酸、酒石酸、クエン酸、グルタミン酸、及びアスパラギン酸からなる群より選ばれる1種以上、より好ましくはコハク酸、乳酸、リンゴ酸及びグリコール酸からなる群より選ばれる1種以上、更に好ましくはコハク酸、リンゴ酸及び乳酸からなる群より選ばれる1種以上、より更に好ましくはリンゴ酸及び乳酸から選ばれる1種以上である、<33>に記載の毛髪処理剤又は頭飾製品用繊維処理剤。 <34> The hair treatment agent or fiber treatment agent for head accessories according to <33>, wherein the organic acid is preferably at least one selected from the group consisting of acetic acid, propionic acid, butanoic acid, benzoic acid, malonic acid, succinic acid, glutaric acid, adipic acid, maleic acid, fumaric acid, phthalic acid, isophthalic acid, polyglutamic acid, lactic acid, malic acid, glycolic acid, hydroxyacrylic acid, glyceric acid, tartaric acid, citric acid, glutamic acid, and aspartic acid, more preferably at least one selected from the group consisting of succinic acid, lactic acid, malic acid, and glycolic acid, even more preferably at least one selected from the group consisting of succinic acid, malic acid, and lactic acid, and even more preferably at least one selected from malic acid and lactic acid.
 <35>有機酸の塩が、好ましくは有機酸のアルカリ金属塩又はアルカリ金属塩、より好ましくはアルカリ金属塩、より好ましくはナトリウム塩及びカリウム塩からなる群より選ばれる1種以上、更に好ましくはナトリウム塩である、<33>又は<34>に記載の毛髪処理剤又は頭飾製品用繊維処理剤。 <35> The hair treatment agent or fiber treatment agent for head accessories according to <33> or <34>, wherein the salt of the organic acid is preferably an alkali metal salt or alkaline metal salt of the organic acid, more preferably an alkali metal salt, more preferably at least one selected from the group consisting of sodium salts and potassium salts, and even more preferably a sodium salt.
 <36>有機酸及び有機酸塩の総量中における有機酸塩の割合が、有機酸換算量として、好ましくは50質量%以下、より好ましくは20質量%以下、更に好ましくは5質量%以下であり、0質量%であってもよい、<33>~<35>のいずれか1項に記載の毛髪処理剤又は頭飾製品用繊維処理剤。 <36> The hair treatment agent or fiber treatment agent for head accessories according to any one of <33> to <35>, wherein the proportion of the organic acid salt in the total amount of the organic acid and the organic acid salt is preferably 50% by mass or less, more preferably 20% by mass or less, and even more preferably 5% by mass or less, calculated as the organic acid equivalent, and may be 0% by mass.
 <37>好ましくは、更に芳香族アルコールを含有し、芳香族アルコールが、好ましくはベンジルアルコール、フェノキシエタノール、及び2-ベンジルオキシエタノールからなる群より選ばれる1種以上である、<1>~<36>のいずれか1項に記載の毛髪処理剤又は頭飾製品用繊維処理剤。 <37> The hair treatment agent or fiber treatment agent for head accessories according to any one of <1> to <36>, further comprising an aromatic alcohol, preferably at least one selected from the group consisting of benzyl alcohol, phenoxyethanol, and 2-benzyloxyethanol.
 <38>芳香族アルコールの含有量が、好ましくは0.01~2質量%、より好ましくは0.05~1質量%、更に好ましくは0.1~0.5質量%である、<37>に記載の毛髪処理剤又は頭飾製品用繊維処理剤。 <38> The hair treatment agent or fiber treatment agent for head accessories according to <37>, wherein the content of the aromatic alcohol is preferably 0.01 to 2 mass%, more preferably 0.05 to 1 mass%, and even more preferably 0.1 to 0.5 mass%.
 <39>成分(A)及び成分(B)以外のカチオン界面活性剤の含有量が、好ましくは1質量%以下、より好ましくは0.5質量%以下、更に好ましくは0.1質量%以下、より更に好ましくは0質量%である、<1>~<38>のいずれか1項に記載の毛髪処理剤又は頭飾製品用繊維処理剤。 <39> The hair treatment agent or fiber treatment agent for head accessories according to any one of <1> to <38>, wherein the content of cationic surfactants other than component (A) and component (B) is preferably 1 mass% or less, more preferably 0.5 mass% or less, even more preferably 0.1 mass% or less, and even more preferably 0 mass%.
 <40>アニオン界面活性剤の含有量が、好ましくは0.5質量%以下、より好ましくは0.1質量%以下、更に好ましくは0.05質量%以下、より更に好ましくは0質量%である、<1>~<39>のいずれか1項に記載の毛髪処理剤又は頭飾製品用繊維処理剤。 <40> The hair treatment agent or fiber treatment agent for head accessories according to any one of <1> to <39>, wherein the content of the anionic surfactant is preferably 0.5% by mass or less, more preferably 0.1% by mass or less, even more preferably 0.05% by mass or less, and even more preferably 0% by mass.
 <41>pHが、好ましくは2.0~7.5、より好ましくは2.5~6.5、更に好ましくは2.5~5.5である、<1>~<40>のいずれか1項に記載の毛髪処理剤又は頭飾製品用繊維処理剤。 <41> The hair treatment agent or fiber treatment agent for head accessories according to any one of <1> to <40>, having a pH of preferably 2.0 to 7.5, more preferably 2.5 to 6.5, and even more preferably 2.5 to 5.5.
 <42>粘度が、好ましくは500~10万mPa・s、より好ましくは1,000~50,000mPa・s、更に好ましくは5,000~40,000mPa・s、より更に好ましくは10,000~30,000mPa・sである、<1>~<41>のいずれか1項に記載の毛髪処理剤又は頭飾製品用繊維処理剤。 <42> The hair treatment agent or fiber treatment agent for head accessories according to any one of <1> to <41>, having a viscosity of preferably 500 to 100,000 mPa·s, more preferably 1,000 to 50,000 mPa·s, even more preferably 5,000 to 40,000 mPa·s, and even more preferably 10,000 to 30,000 mPa·s.
 <43>好ましくは、毛髪又は頭飾製品用繊維に適用した後に洗い流して使用されるものである、<1>~<42>のいずれか1項に記載の毛髪処理剤又は頭飾製品用繊維処理剤。 <43> The hair treatment agent or fiber treatment agent for head accessories according to any one of <1> to <42>, which is preferably applied to hair or fibers for head accessories and then rinsed off before use.
 <44>好ましくは、染色後の毛髪又は頭飾製品用繊維に使用されるものである、<1>~<43>のいずれか1項に記載の毛髪処理剤又は頭飾製品用繊維処理剤。 <44> The hair treatment agent or fiber treatment agent for head accessories according to any one of <1> to <43>, which is preferably used on dyed hair or fibers for head accessories.
 <45><1>~<44>のいずれか1項に記載の毛髪処理剤又は頭飾製品用繊維処理剤を染色後の毛髪又は頭飾製品用繊維に塗布し、水で洗い流す毛髪又は頭飾製品用繊維の処理方法。 <45> A method for treating hair or fibers for head accessories, comprising applying the hair treatment agent or fiber treatment agent for head accessories described in any one of <1> to <44> to dyed hair or fibers for head accessories, and rinsing the hair or fibers for head accessories with water.
 [実施例1~19及び比較例1~8]
 表5~6に示すヘアコンディショナーを下記製造方法にて調製し、以下の方法及び基準に従って、外観観察又は粘度の測定、並びに初回洗浄後及び3回洗浄後における濡れ髪でのコンディショニング効果(コーミングフォース)の持続性の評価を行った。なお、表に記載の含有量は、アクティブ量である。
[Examples 1 to 19 and Comparative Examples 1 to 8]
The hair conditioners shown in Tables 5 and 6 were prepared by the following manufacturing method, and the appearance was observed or the viscosity was measured, and the durability of the conditioning effect (combing force) on wet hair after the first wash and after the third wash was evaluated according to the following methods and criteria. The contents shown in the tables are the active amounts.
 (製造方法)
 表5~6に記載した含有量の各成分を用いて、以下の手順でヘアコンディショナーを調製した。なお、総量500mLのヘアコンディショナーを得るため、各成分は表中の含有量の数値の5倍量(mL)として配合した。
 水を入れた500mLビーカーに、セトリモニウムクロリド(成分(B))又はステアルトリモニウムクロリド(成分(B'))、及び乳酸(全体量のうちの40%)を添加し、56℃で加熱攪拌した。次に、カチオン界面活性剤(成分(A)又は(A'))、高級アルコール(成分(C))、ベンジルアルコールを予め混合し、76℃で溶解させて得られた油性相を添加して、56℃で10分攪拌した。10分攪拌後に加熱を終了し、空冷を開始した。空冷後、各表に記載のシリコーン(成分(D)及び(E))、並びにリンゴ酸と残りの乳酸を添加し、液温が40℃以下になるまで攪拌しながら冷却し、500mLのヘアコンディショナーを得た。
(Production method)
Hair conditioners were prepared in the following manner using the components in the amounts shown in Tables 5 and 6. To obtain a total volume of 500 mL of hair conditioner, each component was mixed in an amount 5 times (mL) the amount shown in the table.
In a 500 mL beaker containing water, cetrimonium chloride (component (B)) or steartrimonium chloride (component (B')), and lactic acid (40% of the total amount) were added and heated and stirred at 56 ° C. Next, a cationic surfactant (component (A) or (A')), a higher alcohol (component (C)), and benzyl alcohol were mixed in advance, and the oily phase obtained by dissolving at 76 ° C. was added and stirred at 56 ° C. for 10 minutes. After stirring for 10 minutes, heating was stopped and air cooling was started. After air cooling, silicones (components (D) and (E)) as shown in each table, as well as malic acid and the remaining lactic acid were added, and the mixture was cooled with stirring until the liquid temperature reached 40 ° C. or less, to obtain 500 mL of hair conditioner.
 (外観評価)
 表5~6に示すヘアコンディショナーを室温で24時間静置し、分離の有無を目視観察した。表中、分離がなく安定であるものを「〇」、分離が認められるものを「×」と表示した。
(Appearance Evaluation)
The hair conditioners shown in Tables 5 and 6 were left to stand at room temperature for 24 hours and visually observed for the presence or absence of separation. In the tables, those that were stable without separation were marked with "O", and those that separated were marked with "X".
 (粘度の測定)
 表5~6に示すヘアコンディショナーの粘度(30℃)は、粘度が10000mPa・s以上の場合には、B型粘度計(東機産業社製、TVB-10)を用い、スピンドル「T-C」、10rpm、1分の条件、粘度が10000mPa・s未満の場合には、BM型粘度計(東機産業社製、TV-10)を用い、ローター「No.3」、12rpm、1分の条件で測定した。
(Viscosity Measurement)
The viscosity (30°C) of the hair conditioners shown in Tables 5 and 6 was measured using a B-type viscometer (manufactured by Toki Sangyo Co., Ltd., TVB-10) with a spindle of "TC", at 10 rpm, and for 1 minute when the viscosity was 10,000 mPa s or more, and using a BM-type viscometer (manufactured by Toki Sangyo Co., Ltd., TV-10) with a rotor of "No. 3", at 12 rpm, and for 1 minute when the viscosity was less than 10,000 mPa s.
 (乾燥後のべたつきのなさの評価)
 ・評価手順
  1.30g日本人トレスを表1に示すプレーンシャンプーで洗髪し、15.0g含水させる。
  2.表5~6に示すヘアコンディショナーを各1mL塗布し、手でなじませて30秒放置した後、15秒すすぐ。
  3.タオルドライ、ドライヤー乾燥の後、5名の専門パネラーで下記に示す評価基準を用いて評価を行い、乾燥後のべたつきのなさを評価した。
(Evaluation of non-stickiness after drying)
Evaluation Procedure 1. Wash 30 g of Japanese tresses with the plain shampoo shown in Table 1, and allow it to absorb 15.0 g of water.
2. Apply 1 mL of each of the hair conditioners shown in Tables 5 and 6, massage with your hands, leave for 30 seconds, and then rinse for 15 seconds.
3. After towel drying and drying with a hair dryer, five expert panelists evaluated the lack of stickiness after drying using the following evaluation criteria.
 〔評価基準〕
  1点:べたつく
  2点:ややべたつく
  3点:どちらともいえない
  4点:あまりべたつかない
  5点:べたつかない
〔Evaluation criteria〕
1 point: Sticky 2 points: Slightly sticky 3 points: Neither sticky nor sticky 4 points: Not very sticky 5 points: Not sticky
 (初回洗浄後の濡れ髪でのコンディショニング効果の持続性の評価方法)
 ・前処理
 30g日本人毛トレスに対し、ヘアカラー剤(表2に示す1液、表3に示す2液を1液:2液=1:1.5で混合して使用)を浴比1:1で塗布し、5分間放置した後、洗い流した。
(Method for evaluating the durability of conditioning effect on wet hair after the first wash)
Pretreatment: A hair coloring agent (liquid 1 shown in Table 2 and liquid 2 shown in Table 3 were mixed at a ratio of 1:1.5) was applied to 30 g of Japanese hair tresses in a bath ratio of 1:1, left for 5 minutes, and then washed off.
 ・評価手順
  1.上記前処理後の30g日本人毛トレスを表1に示すプレーンシャンプーで洗髪した後すすぎ、15.0g含水させた。
  2.表5~6に示すヘアコンディショナーを各1mL塗布し、手でなじませて30秒放置した後、15秒すすいだ。
  3.タオルドライ、ドライヤー乾燥の後、表1に示すプレーンシャンプー1mLで表裏20回ずつこすって30秒間洗髪した後、15秒間すすいだ。その後、表4に示すプレーンリンス1mLを30秒間なじませ、15秒間すすいだ。
  4.ブラシでトレスの絡まりを完全に梳いてから、含水量を15gに調節した。
  5.一定の速度(1秒に1回)にて、ブラシで30回コーミングしたときのコーミングフォースを、ダイナミックコーミングフォース法(鈴木ら; J. Soc. Cosmet. Chem. Japan. Vol. 27, No.1, P11-13, 1993)により測定し、30回の測定値(最大値)の平均を求めて、コンディショニング効果の持続性の評価の指標とした。コーミングフォースの値が小さいほど櫛通りが良く、滑らかであることを示している。
Evaluation Procedure 1. After the above pretreatment, 30 g of Japanese hair tress was washed with the plain shampoo shown in Table 1, rinsed, and allowed to absorb 15.0 g of water.
2. 1 mL of each of the hair conditioners shown in Tables 5 and 6 was applied, massaged into the hair with the hands, left on for 30 seconds, and then rinsed for 15 seconds.
3. After towel drying and drying with a hair dryer, the hair was washed for 30 seconds by rubbing the front and back 20 times with 1 mL of plain shampoo shown in Table 1, and then rinsed for 15 seconds. Then, 1 mL of plain rinse shown in Table 4 was applied for 30 seconds, and rinsed for 15 seconds.
4. The tresses were thoroughly detangled with a brush and then the moisture content was adjusted to 15g.
5. The combing force when combing 30 times with a brush at a constant speed (once per second) was measured using the dynamic combing force method (Suzuki et al.; J. Soc. Cosmet. Chem. Japan. Vol. 27, No.1, pp. 11-13, 1993), and the average of the 30 measured values (maximum value) was calculated and used as an index for evaluating the durability of the conditioning effect. The smaller the combing force value, the easier and smoother the combing process.
 (3回洗浄後の濡れ髪でのコンディショニング効果の持続性の評価方法)
 評価手順の3.を計3回繰り返した以外、上記「処理直後の濡れ髪でのコンディショニング効果の持続性の評価方法」と同様にしてコーミングフォースを測定し、評価を行った。
(Method for evaluating durability of conditioning effect on wet hair after three washes)
The combing force was measured and the evaluation was performed in the same manner as in the above "Method of evaluating the durability of conditioning effect on wet hair immediately after treatment", except that step 3 of the evaluation procedure was repeated a total of three times.
 なお、上記手順2のヘアコンディショナーとして表4に示すプレーンリンスを使用した場合のトレスのコーミングフォースを参考例として各表に記載した。 In addition, the combing force of tresses when using the plain rinse shown in Table 4 as the hair conditioner in step 2 above is listed in each table as a reference example.
Figure JPOXMLDOC01-appb-T000019
 
Figure JPOXMLDOC01-appb-T000019
 
Figure JPOXMLDOC01-appb-T000020
 
Figure JPOXMLDOC01-appb-T000020
 
Figure JPOXMLDOC01-appb-T000021
 
Figure JPOXMLDOC01-appb-T000021
 
Figure JPOXMLDOC01-appb-T000022
 
Figure JPOXMLDOC01-appb-T000022
 
Figure JPOXMLDOC01-appb-T000023
 
Figure JPOXMLDOC01-appb-T000023
 
Figure JPOXMLDOC01-appb-T000024
Figure JPOXMLDOC01-appb-T000024
  *1:ファーミンDM-E80、花王社製
  *2:アミデットAPA22、花王スペイン社製
  *3:コータミン2285E、花王社製
  *4:カワソフトEP59S、川研ファインケミカル社製
  *5:コータミン60W、花王社製
  *6:コータミン86W、花王社製
  *7:カルコール8098、花王社製
  *8:シリコーンSF 8457 C、ダウ・東レ社製
  *9:シリコーン KHS-3、信越化学工業社製
  *10:シリコーン KHS-9、信越化学工業社製
 
 
*1: Farmin DM-E80, manufactured by Kao Corporation *2: Amidet APA22, manufactured by Kao Spain S.A. *3: Coatamin 2285E, manufactured by Kao Corporation *4: Kawasoft EP59S, manufactured by Kawaken Fine Chemicals S.A. *5: Coatamin 60W, manufactured by Kao Corporation *6: Coatamin 86W, manufactured by Kao Corporation *7: Kalcol 8098, manufactured by Kao Corporation *8: Silicone SF 8457 C, manufactured by Dow Toray Co., Ltd. *9: Silicone KHS-3, manufactured by Shin-Etsu Chemical Co., Ltd. *10: Silicone KHS-9, manufactured by Shin-Etsu Chemical Co., Ltd.

Claims (10)

  1.  次の成分(A)~(C)、並びに成分(D)及び成分(E)から選択される1種以上を含有し、成分(D)及び成分(E)の合計含有量が1質量%以上15質量%以下である、毛髪処理剤又は頭飾製品用繊維処理剤。
     (A) エーテルアミン又はその塩、アミドアミン又はその塩、及び炭素数18以上のアルキル基を有するモノ長鎖アルキル第4級アンモニウム塩からなる群より選ばれる1種以上のカチオン界面活性剤
     (B) 炭素数16以下のアルキル基を有するモノ長鎖アルキル第4級アンモニウム塩 0.1質量%以上2.8質量%以下
     (C) 高級アルコール 1質量%以上15質量%以下
     (D) アミノ変性シリコーン及びアミノポリエーテル変性シリコーンからなる群より選ばれる1種以上の変性シリコーン
     (E) ジメチコン
    A hair treatment agent or a fiber treatment agent for a head accessory product, comprising one or more components selected from the following components (A) to (C), as well as components (D) and (E), wherein the total content of components (D) and (E) is 1% by mass or more and 15% by mass or less.
    (A) One or more cationic surfactants selected from the group consisting of ether amines or their salts, amido amines or their salts, and mono-long-chain alkyl quaternary ammonium salts having an alkyl group with 18 or more carbon atoms. (B) Mono-long-chain alkyl quaternary ammonium salts having an alkyl group with 16 or less carbon atoms, 0.1% by mass or more and 2.8% by mass or less. (C) Higher alcohol, 1% by mass or more and 15% by mass or less. (D) One or more modified silicones selected from the group consisting of amino-modified silicones and aminopolyether-modified silicones. (E) Dimethicone.
  2.  成分(D)及び(E)の合計含有量が1質量%以上10質量%以下である、請求項1に記載の毛髪処理剤又は頭飾製品用繊維処理剤。 The hair treatment agent or fiber treatment agent for head accessories according to claim 1, wherein the total content of components (D) and (E) is 1% by mass or more and 10% by mass or less.
  3.  成分(A)に対する成分(B)の質量比(B)/(A)が0.01以上1.2以下である、請求項1又は2に記載の毛髪処理剤又は頭飾製品用繊維処理剤。 The hair treatment agent or fiber treatment agent for head accessories according to claim 1 or 2, in which the mass ratio (B)/(A) of component (B) to component (A) is 0.01 or more and 1.2 or less.
  4.  成分(D)及び成分(E)を含有する、請求項1~3のいずれか1項に記載の毛髪処理剤又は頭飾製品用繊維処理剤。 The hair treatment agent or fiber treatment agent for head accessories according to any one of claims 1 to 3, containing component (D) and component (E).
  5.  成分(D)に対する成分(E)の質量比(E)/(D)が0.1以上15.0以下である、請求項1~4のいずれか1項に記載の毛髪処理剤又は頭飾製品用繊維処理剤。 The hair treatment agent or fiber treatment agent for head accessories according to any one of claims 1 to 4, wherein the mass ratio (E)/(D) of component (E) to component (D) is 0.1 or more and 15.0 or less.
  6.  成分(B)が、炭素数12以上16以下のアルキル基を有するモノ長鎖アルキル第4級アンモニウム塩である、請求項1~5のいずれか1項に記載の毛髪処理剤又は頭飾製品用繊維処理剤。 The hair treatment agent or fiber treatment agent for head accessories according to any one of claims 1 to 5, wherein component (B) is a mono-long-chain alkyl quaternary ammonium salt having an alkyl group having 12 to 16 carbon atoms.
  7.  成分(B)の含有量が0.3質量%以上2.3質量%以下である、請求項1~6のいずれか1項に記載の毛髪処理剤又は頭飾製品用繊維処理剤。 The hair treatment agent or fiber treatment agent for head accessories according to any one of claims 1 to 6, wherein the content of component (B) is 0.3% by mass or more and 2.3% by mass or less.
  8.  成分(E)が、25℃における動粘度が3万mm2/s以上20万mm2/s以下のジメチコンである、請求項1~7のいずれか1項に記載の毛髪処理剤又は頭飾製品用繊維処理剤。 8. The hair treatment agent or fiber treatment agent for head ornament products according to any one of claims 1 to 7, wherein component (E) is dimethicone having a kinetic viscosity at 25°C of 30,000 mm 2 /s or more and 200,000 mm 2 /s or less.
  9.  染色後の毛髪又は頭飾製品用繊維に使用されるものである請求項1~8のいずれか1項に記載の毛髪処理剤又は頭飾製品用繊維処理剤。 The hair treatment agent or fiber treatment agent for head accessories according to any one of claims 1 to 8, which is used on dyed hair or fibers for head accessories.
  10.  請求項1~8のいずれか1項に記載の毛髪処理剤又は頭飾製品用繊維処理剤を染色後の毛髪又は頭飾製品用繊維に塗布し、水で洗い流す毛髪又は頭飾製品用繊維の処理方法。 A method for treating hair or fibers for head accessories, comprising applying the hair treatment agent or fiber treatment agent for head accessories described in any one of claims 1 to 8 to dyed hair or fibers for head accessories, and rinsing the hair or fibers for head accessories with water.
PCT/JP2023/030870 2022-09-29 2023-08-28 Hair treatment agent or head decoration product fiber treatment agent WO2024070386A1 (en)

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Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2005187400A (en) * 2003-12-25 2005-07-14 Lion Corp Hair cosmetic for preventing cuticle from peeling off
JP2016216432A (en) * 2015-05-26 2016-12-22 花王株式会社 Hair cosmetic
JP2017105760A (en) * 2015-12-02 2017-06-15 花王株式会社 Hair Cosmetics

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2005187400A (en) * 2003-12-25 2005-07-14 Lion Corp Hair cosmetic for preventing cuticle from peeling off
JP2016216432A (en) * 2015-05-26 2016-12-22 花王株式会社 Hair cosmetic
JP2017105760A (en) * 2015-12-02 2017-06-15 花王株式会社 Hair Cosmetics

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