WO2017094625A1 - Hair cosmetic - Google Patents

Hair cosmetic Download PDF

Info

Publication number
WO2017094625A1
WO2017094625A1 PCT/JP2016/085039 JP2016085039W WO2017094625A1 WO 2017094625 A1 WO2017094625 A1 WO 2017094625A1 JP 2016085039 W JP2016085039 W JP 2016085039W WO 2017094625 A1 WO2017094625 A1 WO 2017094625A1
Authority
WO
WIPO (PCT)
Prior art keywords
hair
acid
group
mass
component
Prior art date
Application number
PCT/JP2016/085039
Other languages
French (fr)
Japanese (ja)
Inventor
晶子 松藤
健介 青柳
Original Assignee
花王株式会社
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by 花王株式会社 filed Critical 花王株式会社
Priority to SG11201804615SA priority Critical patent/SG11201804615SA/en
Publication of WO2017094625A1 publication Critical patent/WO2017094625A1/en

Links

Classifications

    • 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
    • A61K8/72Cosmetics 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
    • A61K8/891Polysiloxanes saturated, e.g. dimethicone, phenyl trimethicone, C24-C28 methicone or stearyl dimethicone
    • A61K8/894Polysiloxanes saturated, e.g. dimethicone, phenyl trimethicone, C24-C28 methicone or stearyl dimethicone modified by a polyoxyalkylene group, e.g. cetyl dimethicone copolyol
    • 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 cosmetic that is washed off after being applied to hair.
  • Patent Documents 1 and 2 disclose a hair conditioner that is excellent in touch and that contains a cationic surfactant, a higher alcohol, an oil and fat, silicone, and the like.
  • Patent Document 2 discloses a hair conditioning composition in which volatile silicone M3T (methyltrimethicone), a nonvolatile silicone derivative and a cationic surfactant are combined.
  • Patent Document 3 discloses an optically transparent hair treatment agent containing a hydrophobic silicone compound and a hydrophilic silicone compound, as well as various active agents and polymers.
  • Patent Document 1 JP-A-6-172131 (Patent Document 2) JP-A-2006-265205 (Patent Document 3) JP-T 2008-520614
  • the present invention provides a hair cosmetic containing components (A) to (D) and water, which is used after being applied to hair and washed away.
  • the present invention also provides a hair treatment method in which the above-described hair cosmetic is applied to the hair and washed away with water.
  • hair damage caused by hair sets using heat such as hair irons and hair dryers which has become a habit mainly among young women, has become serious. It is known that hair damage is accompanied by the loss of 18-MEA (18-methyleicosanoic acid), which is a fatty acid covering the hair surface, and causes increased surface friction as the hair surface becomes hydrophilic. Damaged and hydrophilized hair not only loses its smoothness but also becomes difficult to dry after shampooing, and it takes a long time to dry with a dryer or the like, which is a physical burden. In addition, wet damaged hair tends to get entangled, and the catches that occur during drying of the dryer add to the accumulation of further damage and the psychological burden on the consumer.
  • 18-MEA 18-methyleicosanoic acid
  • the present invention makes it easy to disperse each piece of wet hair, regardless of the type of cationic surfactant contained, by washing it after applying it to the hair after shampooing.
  • the present invention relates to a hair cosmetic that can be dried over time and has excellent smoothness during rinsing.
  • “Hair dispersal” is important as a factor to increase the drying speed of hair after washing. That is, when the hair is dispersed, the contact area with the towel increases when the towel is dried, and moisture of the hair is absorbed quickly by the towel, and when the dryer is dried (even during natural drying), the contact area with the air is increased. Will increase and the moisture of the hair will evaporate quickly.
  • the present inventors have used an amino-polyether co-modified silicone having a specific structure and a volatile silicone in combination to produce an adhesive component on the hair. It has been found that the amount of adsorption is reduced and the bulky adhesive component hardly adheres to the hair. As a result, the present inventors have found that the adhesiveness of each hair can be weakened, wet hair after treatment becomes extremely easy to disperse, and the drying speed can be dramatically improved without tangling.
  • Component (A) Cationic surfactant
  • cationic surfactant of component (A) include (i) alkyltrimethylammonium salt, (ii) alkoxyalkyltrimethylammonium salt, (iii) dialkyldimethylammonium salt, (iv) alkyldimethylamine and salts thereof, ( v) alkoxyalkyldimethylamine and its salt, (vi) alkylamidoalkyldimethylamine and its salt, and the like.
  • alkyltrimethylammonium salt examples include those represented by the following general formula (1).
  • R 1 represents an alkyl group having 12 to 22 carbon atoms
  • X ⁇ represents a halide ion such as a chloride ion or a bromide ion; a methosulphate ion, an ethosulphate ion, a methosphosphate ion, an ethosphosphate ion. , Methocarbonate ions and the like.
  • cetyltrimethylammonium chloride stearyltrimethylammonium chloride, behenyltrimethylammonium chloride, behenyltrimethylammonium methosulfate and the like.
  • alkoxyalkyltrimethylammonium salt examples include those represented by the following general formula (2).
  • R 2 O—R 3 —N + (CH 3 ) 3 X ⁇ (2)
  • R 3 represents an ethylene group or a propylene group optionally substituted by a hydroxy group
  • X ⁇ represents a halogen such as a chloride ion or a bromide ion.
  • Compound ion; methosulphate ion, ethosulphate ion, methosphosphate ion, ethosphosphate ion, methcarbonate ion, etc.
  • Specific examples include stearoxypropyltrimethylammonium chloride, stearoxyethyltrimethylammonium chloride, stearoxyhydroxypropyltrimethylammonium chloride, and the like.
  • dialkyldimethylammonium salt examples include those represented by the following general formula (3).
  • R 4 independently represents an alkyl group having 12 to 22 carbon atoms or a benzyl group, and X ⁇ represents a halide ion such as a chloride ion or a bromide ion; a methosulphate ion, an ethosulphate ion, or a methophos ion.
  • ions include fate ions, ethophosphate ions, methocarbonate ions, and the like.
  • Specific examples include distearyl dimethyl ammonium chloride.
  • alkyldimethylamine and its salt Alkyldimethylamine reacts with an acid to form a quaternary ammonium salt, which becomes a surfactant. Therefore, alkyldimethylamine and its salt are defined here as a cationic surfactant. Moreover, the content is converted by the mass of alkyldimethylamine. Examples of alkyldimethylamine and salts thereof include those represented by the following general formula (4) and salts thereof. R 5 —N (CH 3 ) 2 (4) [Wherein R 5 represents an alkyl group having 12 to 22 carbon atoms. ]
  • Examples of the salt include salts with organic acids or inorganic acids.
  • Examples of the organic acid include monocarboxylic acids such as acetic acid and propionic acid; dicarboxylic acids such as malonic acid, succinic acid, glutaric acid, adipic acid, maleic acid, fumaric acid, and phthalic acid; polycarboxylic acids such as polyglutamic acid; Examples thereof include hydroxycarboxylic acids such as glycolic acid, lactic acid, hydroxyacrylic acid, glyceric acid, malic acid, tartaric acid and citric acid; acidic amino acids such as glutamic acid and aspartic acid.
  • Examples of the inorganic acid include hydrochloric acid, sulfuric acid, phosphoric acid and the like.
  • organic acids are preferable, dicarboxylic acids, hydroxycarboxylic acids, and acidic amino acids are preferable.
  • dicarboxylic acids maleic acid and succinic acid are more preferable.
  • hydroxycarboxylic acid glycolic acid, lactic acid, and malic acid are more preferable.
  • acidic amino acid glutamic acid is more preferable.
  • alkyldimethylamine and salts thereof include N, N-dimethylbehenylamine, N, N-dimethylstearylamine, and organic acid salts thereof.
  • N, N-dimethylbehenylamine lactate, N, N-dimethylstearylamine glycolate and the like are preferred.
  • alkoxyalkyldimethylamine and salts thereof Alkoxyalkyldimethylamine reacts with an acid to form a quaternary ammonium salt, which becomes a surfactant. Accordingly, alkoxyalkyldimethylamine and its salts are defined herein as cationic surfactants. Moreover, the content is converted with the mass of alkoxyalkyl dimethylamine. Examples of the alkoxyalkyldimethylamine and salts thereof include those represented by the following general formula (5) and salts thereof. R 6 —O—R 7 —N (CH 3 ) 2 (5) [Wherein R 6 represents an alkyl group having 12 to 22 carbon atoms, and R 7 represents an ethylene group or a propylene group. ]
  • Examples of the salt include salts with organic acids or inorganic acids.
  • Examples of the organic acid include monocarboxylic acids such as acetic acid and propionic acid; dicarboxylic acids such as malonic acid, succinic acid, glutaric acid, adipic acid, maleic acid, fumaric acid, and phthalic acid; polycarboxylic acids such as polyglutamic acid; Examples thereof include hydroxycarboxylic acids such as glycolic acid, lactic acid, hydroxyacrylic acid, glyceric acid, malic acid, tartaric acid and citric acid; acidic amino acids such as glutamic acid and aspartic acid.
  • Examples of the inorganic acid include hydrochloric acid, sulfuric acid, phosphoric acid and the like.
  • organic acids are preferable, dicarboxylic acids, hydroxycarboxylic acids, and acidic amino acids are preferable.
  • dicarboxylic acids maleic acid and succinic acid are more preferable.
  • hydroxycarboxylic acid glycolic acid, lactic acid, and malic acid are more preferable.
  • acidic amino acid glutamic acid is more preferable.
  • alkoxyalkyldimethylamines and salts thereof include N, N-dimethyl-3-hexadecyloxypropylamine, N, N-dimethyl-3-octadecyloxypropylamine and organic acid salts thereof, N N, N-dimethyl-3-hexadecyloxypropylamine lactate and N, N-dimethyl-3-octadecyloxypropylamine glycolate are preferred.
  • alkylamidoalkyldimethylamine and its salt Alkylamidoalkyldimethylamine reacts with an acid to form a quaternary ammonium salt to become a surfactant. Therefore, herein, alkylamidoalkyldimethylamine and salts thereof are defined as cationic surfactants. Moreover, the content is converted with the mass of alkylamide alkyl dimethylamine. Examples of the alkylamidoalkyldimethylamine and salts thereof include those represented by the following general formula (6) and salts thereof.
  • R 8 CONH— (CH 2 ) m —N (CH 3 ) 2 (6) [Wherein R 8 represents an alkyl group having 12 to 22 carbon atoms, and m represents a number of 2 to 4. ]
  • R 8 is preferably an alkyl group having 14 to 22 carbon atoms, and preferably an alkyl group having 16 to 20 carbon atoms, from the viewpoint of smoothness during rinsing and difficulty in entanglement during drying of the dryer. Those are more preferred.
  • the salt include salts with organic acids or inorganic acids.
  • Examples of the organic acid include monocarboxylic acids such as acetic acid and propionic acid; dicarboxylic acids such as malonic acid, succinic acid, glutaric acid, adipic acid, maleic acid, fumaric acid, and phthalic acid; polycarboxylic acids such as polyglutamic acid; Examples thereof include hydroxycarboxylic acids such as glycolic acid, lactic acid, hydroxyacrylic acid, glyceric acid, malic acid, tartaric acid and citric acid; acidic amino acids such as glutamic acid and aspartic acid.
  • Examples of the inorganic acid include hydrochloric acid, sulfuric acid, phosphoric acid and the like.
  • organic acids are preferable, dicarboxylic acids, hydroxycarboxylic acids, and acidic amino acids are preferable.
  • dicarboxylic acids maleic acid and succinic acid are more preferable.
  • hydroxycarboxylic acid glycolic acid, lactic acid, and malic acid are more preferable.
  • acidic amino acid glutamic acid is more preferable.
  • alkylamidoalkyldimethylamine and salts thereof include N- (3- (dimethylamino) propyl) docosanamide and salts thereof, and N- (3- (dimethylamino) propyl) stearamide and salts thereof.
  • alkyltrimethylammonium salt (i) alkyltrimethylammonium salt, (ii) alkoxyalkyltrimethylammonium salt, (v) alkoxyalkyldimethylamine and salt thereof, (vi) alkylamidoalkyldimethylamine and salt thereof are preferable, and dried.
  • alkoxyalkyldimethylamine and its salt (v) alkoxyalkyldimethylamine and its salt, and (vi) alkylamidoalkyldimethylamine and its salt are preferable.
  • N, N-dimethyl-3-hexadecyloxypropylamine and its salts are considered from the viewpoints of smoothness during rinsing, ease of hair bundling, difficulty in entanglement during dryer drying, and speed of drying.
  • N, N-dimethyl-3-octadecyloxypropylamine and its salt, N- (3- (dimethylamino) propyl) docosanamide and its salt, N- (3- (dimethylamino) propyl) stearamide and its salt are preferable .
  • Component (A) cationic surfactant can be used alone or in combination of two or more.
  • the content of the component (A) in the hair cosmetic composition of the present invention is preferably 0.1% by mass or more, more preferably 0.5% by mass or more, and still more preferably 0.75% from the viewpoint of smoothness when using a conditioner and appropriate quick drying performance. It is preferably 10% by mass or less, more preferably 8% by mass or less, still more preferably 6% by mass or less, still more preferably 4% by mass or less, and further preferably 3% by mass or less.
  • Component (B) Higher alcohol
  • the higher alcohol of component (B) may be linear and branched, or saturated and unsaturated aliphatic alcohols, and the carbon number thereof is preferably 10 or more, more preferably 14 or more, and still more preferably 16 In addition, it is preferably 22 or less, more preferably 20 or less, and still more preferably 18 or less.
  • Specific examples include lauryl alcohol, myristyl alcohol, cetyl alcohol, stearyl alcohol, aralkyl alcohol, hexyl decanol, isostearyl alcohol, oleyl alcohol, 2-octyldodecanol and the like. Of these, stearyl alcohol, cetyl alcohol, and myristyl alcohol are preferred. These higher alcohols can be used alone or in combination of two or more.
  • the content of the component (B) in the hair cosmetic composition of the present invention is preferably 1% by mass or more, more preferably 2% by mass or more, and further preferably 3% from the viewpoint of smoothness from application to rinsing and after drying. From the viewpoint of quick drying performance, stickiness control after drying, and adjustment to an easy-to-use viscosity, it is preferably 10% by mass or less, more preferably 8% by mass or less, and even more preferably 7% by mass or less. More preferably, it is 6 mass% or less.
  • Component (C) Silicone having polyoxyalkylene side chain and aminoalkyl side chain
  • Examples of the silicone having a polyoxyalkylene side chain and an aminoalkyl side chain as component (C) include those represented by the following general formula (7).
  • R 9 represents a divalent hydrocarbon group having 1 to 6 carbon atoms
  • R 10 represents a substituent having an amino group or an ammonium group represented by —R 11 Z.
  • R 11 represents a divalent hydrocarbon group having 1 to 6 carbon atoms
  • Z represents —NR 12 2 , —NR 12 (CH 2 ) c NR 12 2
  • —NR 12 (CH 2 ) c NR 12 represents a monovalent group selected from the group consisting of C ⁇ O (R 13 )
  • R 12 represents a hydrogen atom or a hydrocarbon group having 1 to 4 carbon atoms
  • R 13 represents a hydrocarbon having 1 to 4 carbon atoms.
  • C represents an integer of 2 to 6
  • R 14 represents a hydrocarbon group having 1 to 4 carbon atoms or a trimethylsilyl group.
  • R 9 is a divalent hydrocarbon group having 2 to 4 carbon atoms
  • R 10 is —R 11 —NH 2
  • R 11 is a divalent hydrocarbon group having 2 to 4 carbon atoms
  • R 12 and It is preferable that each R 14 is independently a methyl group or an ethyl group.
  • the viscosity at 25 ° C. of component (C), a single one hair wet very loose and easy to improve the finger combability, yet from the viewpoint of the excellent in smoothness during rinsing preferably 4000 mm 2 / s or less, more preferably 3000 mm 2 / s or less, further preferably 2000 mm 2 / s or less, more preferably 1000 mm 2 / s or less, more preferably 800 mm 2 / s or less, and preferably 100 mm 2 / s or more. More preferably, it is 200 mm 2 / s or more.
  • the viscosity at 25 ° C was measured using a capillary viscometer, and the time for a certain volume of liquid to flow through the capillary of the viscometer at 25 ° C and 1013.25 hPa was measured. Is calculated using The capillary viscometer is generally of a type such as Ubbelohde or Canon-Fenske.
  • Viscosity (mm 2 / s) Outflow time (seconds) x Viscometer constant
  • component (C) examples include ABIL SOFT AF100 (Evonik Industry Co., Ltd .: viscosity 400 mm 2 / s), X-22-3939A (Shin-Etsu Chemical Co., Ltd .: viscosity 2,800 mm 2 / s), Silsense A21 (Lubrisol) (Manufactured by company: viscosity 250 mm 2 / s).
  • the silicone having a polyoxyalkylene side chain and an aminoalkyl side chain can be used alone or in combination of two or more.
  • the content of the component (C) in the hair cosmetic composition of the present invention is preferably 0.05% by mass or more, more preferably 0.1%, from the viewpoint of easily spreading wet hair, preventing tangling, and drying the hair in a short time. % By mass or more, more preferably 0.2% by mass or more, more preferably 0.3% by mass or more.
  • the viscosity is preferably 5% by mass or less, more preferably 4% by mass or less, still more preferably 3% by mass or less, and further preferably 2.5% by mass or less.
  • Component (D): Volatile silicone As the volatile silicone of component (D), one or more selected from the group consisting of linear and cyclic silicone oils having a boiling point of 260 ° C. or lower under 1013.25 hPa can be used. Further, from the viewpoint of stability during storage, the boiling point under 1013.25 hPa is preferably 35 ° C. or higher.
  • chain volatile silicone examples include chain silicones represented by the following formula (8) or the following general formula (9), and examples of the cyclic volatile silicone include those represented by the following general formula (10). And cyclic silicone.
  • methyltrimethicone represented by the formula (8) is preferable from the viewpoint of making each wet hair very easy to disperse, improving finger passage, and excellent smoothness during rinsing. .
  • the volatile silicone of component (D) can be used alone or in combination of two or more.
  • the content of the component (D) in the hair cosmetic composition of the present invention is preferably 0.05% by mass or more, more preferably 0.1%, from the viewpoint of making it easy to disperse wet hair, preventing tangling, and drying the hair in a short time. It is preferably 10% by mass or less, more preferably 0.5% by mass or more, and from the viewpoint of ease of hair dispersion, speed of drying, suppression of squeezing during rinsing, and suppression of stickiness after drying. More preferably, it is 8 mass% or less, More preferably, it is 6 mass% or less, More preferably, it is 4 mass% or less, More preferably, it is 3 mass% or less, More preferably, it is 2 mass% or less.
  • the mass ratio (C) / (D) of component (C) to component (D) allows the conditioning component to be evenly adsorbed to the entire hair surface and weakens the adhesiveness of each hair. From the viewpoint of making the later wet hair very easy to disperse and dramatically improving the drying speed without entanglement, it is preferably 0.01 or more, more preferably 0.05 or more, further preferably 0.08 or more, more preferably 0.1 or more, still more preferably. Is 0.2 or more, preferably 5 or less, more preferably 4 or less, still more preferably 3 or less, still more preferably 2 or less, still more preferably 1 or less, still more preferably 0.8 or less.
  • the hair cosmetic composition of the present invention contains water as a medium. Water is the remaining amount of components (A) to (D) and other components.
  • the hair cosmetic of the present invention may further contain other components generally used in hair cosmetics depending on the purpose.
  • Antidandruff agent pH adjuster; vitamin agent; bactericidal agent; anti-inflammatory agent; antiseptic agent; chelating agent; moisturizer such as panthenol; colorant such as dye and pigment; Polar solvent extract, protein obtained from shells or pearls having a pearl layer or hydrolyzate thereof, protein obtained from silk or hydrolyzate thereof, protein-containing extract obtained from legume seeds, ginseng extract, Extracts such as rice germ extract, hibamata extract, camellia extract, aloe extract, moon peach leaf extract, chlorella extract; pearl powder such as mica titanium; refreshing agent such as menthol: fragrance; pigment; UV absorption Agents; antioxidants; and other components described in ENCYCLOPEDIA OF SHAMPOO INGREDIENTS (MICELLE PRESS).
  • the pH of the hair cosmetic composition of the present invention is preferably 2.0 or more, more preferably 2.5 or more, and preferably 7.5 or less, more preferably 6.5 or less, and further preferably 5.5 or less.
  • the pH of the hair cosmetic refers to a value at 25 ° C. when diluted 20 times by weight with water.
  • the hair cosmetic composition of the present invention is used after being applied to the hair and washed away, and examples thereof include those used in the bathroom such as hair rinse, hair conditioner, hair treatment, hair pack and the like.
  • the hair cosmetic composition of the present invention is applied to the hair and then washed away with water. Thereby, it is excellent in the smoothness at the time of a rinse, and makes it easy to disperse each wet hair one by one, it is good to pass through a finger without entanglement, and hair can be dried in a short time.
  • a hair cosmetic comprising components (A) to (D) and water, which is used after being applied to hair and washed away.
  • Component (A) is preferably alkyltrimethylammonium salt, alkoxyalkyltrimethylammonium salt, dialkyldimethylammonium salt, alkyldimethylamine and its salt, alkoxyalkyldimethylamine and its salt, and alkylamidoalkyldimethylamine and its Hair cosmetic according to ⁇ 1>, which is one or more compounds selected from the group consisting of salts.
  • the content of component (A) is preferably 0.1% by mass or more, more preferably 0.5% by mass or more, still more preferably 0.75% by mass or more, and preferably 10% by mass or less, more preferably 8% by mass.
  • the hair cosmetic composition according to ⁇ 1> or ⁇ 2> which is not more than mass%, more preferably not more than 6 mass%, still more preferably not more than 4 mass%, still more preferably not more than 3 mass%.
  • Component (B) is preferably 10 or more carbon atoms, more preferably 14 or more carbon atoms, still more preferably 16 or more carbon atoms, and preferably 22 or less carbon atoms, more preferably 20 or less carbon atoms,
  • the content of component (B) is preferably 1% by mass or more, more preferably 2% by mass or more, still more preferably 3% by mass or more, and preferably 10% by mass or less, more preferably 8% by mass.
  • ⁇ 6> The hair cosmetic according to any one of ⁇ 1> to ⁇ 5>, wherein the component (C) is preferably represented by the following general formula (7).
  • R 9 represents a divalent hydrocarbon group having 1 to 6 carbon atoms
  • R 10 represents a substituent having an amino group or an ammonium group represented by —R 11 Z.
  • R 11 represents a divalent hydrocarbon group having 1 to 6 carbon atoms
  • Z represents —NR 12 2 , —NR 12 (CH 2 ) c NR 12 2
  • —NR 12 (CH 2 ) c NR 12 represents a monovalent group selected from the group consisting of C ⁇ O (R 13 )
  • R 12 represents a hydrogen atom or a hydrocarbon group having 1 to 4 carbon atoms
  • R 13 represents a hydrocarbon having 1 to 4 carbon atoms.
  • C represents an integer of 2 to 6
  • R 14 represents a hydrocarbon group having 1 to 4 carbon atoms or a trimethylsilyl group.
  • the viscosity of component (C) at 25 ° C. is preferably 4000 mm 2 / s or less, more preferably 3000 mm 2 / s or less, still more preferably 2000 mm 2 / s or less, more preferably 1000 mm 2 / s or less,
  • the content of component (C) is preferably 0.05% by mass or more, more preferably 0.1% by mass or more, still more preferably 0.2% by mass or more, further preferably 0.3% by mass or more, and preferably 5%.
  • Component (D) is preferably one or more selected from the group consisting of linear and cyclic silicone oils having a boiling point of 260 ° C. or lower under 1013.25 hPa ⁇ 1> to ⁇ 8>
  • the hair cosmetic composition according to any one of the above.
  • Component (D) preferably comprises a chain silicone represented by formula (8), a chain silicone represented by formula (9), and a cyclic silicone represented by formula (10) Hair cosmetic according to ⁇ 9>, which is one or more volatile silicones selected from the group.
  • the content of component (D) is preferably 0.05% by mass or more, more preferably 0.1% by mass or more, still more preferably 0.5% by mass or more, and preferably 10% by mass or less, more preferably 8% by mass.
  • ⁇ 1> to ⁇ 10> which is not more than mass%, more preferably not more than 6 mass%, still more preferably not more than 4 mass%, still more preferably not more than 3 mass%, still more preferably not more than 2 mass%.
  • the mass ratio (C) / (D) of the component (C) to the component (D) is preferably 0.01 or more, more preferably 0.05 or more, still more preferably 0.08 or more, still more preferably 0.1 or more, and still more preferably. It is 0.2 or more, preferably 5 or less, more preferably 4 or less, further preferably 3 or less, further preferably 2 or less, still more preferably 1 or less, and further preferably 0.8 or less.
  • ⁇ 1> to ⁇ 11> The hair cosmetic composition according to any one of the above.
  • the pH at 25 ° C. when diluted 20 times by mass with water is preferably 2.0 or more, more preferably 2.5 or more, preferably 7.5 or less, more preferably 6.5 or less, and even more preferably 5.5 or less.
  • ⁇ 14> A hair treatment method in which the hair cosmetic composition according to any one of ⁇ 1> to ⁇ 13> is applied to hair and washed away with water.

Landscapes

  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Birds (AREA)
  • Epidemiology (AREA)
  • Dermatology (AREA)
  • Emergency Medicine (AREA)
  • Cosmetics (AREA)
  • Compositions Of Macromolecular Compounds (AREA)

Abstract

A hair cosmetic which contains components (A)-(D) and water, and is used by being applied to hair and then rinsed away. (A) a cation surfactant, (B) a higher alcohol, (C) a silicone having a polyoxyalkylene side chain and an amino alkyl side chain, and (D) a volatile silicone.

Description

毛髪化粧料Hair cosmetics
 本発明は、毛髪に適用した後、洗い流すタイプの毛髪化粧料に関する。 The present invention relates to a hair cosmetic that is washed off after being applied to hair.
 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1~2には、カチオン界面活性剤、高級アルコール、油脂、シリコーン等を配合した、感触に優れるヘアコンディショナーが開示されている。 The type of hair cosmetics to be washed away, such as hair rinses and hair conditioners, used after shampooing the hair, is based on cationic surfactants and higher alcohols, and provides a smooth and moist feel to the hair to condition the surface of the hair. It is aimed. For example, Patent Documents 1 and 2 disclose a hair conditioner that is excellent in touch and that contains a cationic surfactant, a higher alcohol, an oil and fat, silicone, and the like.
 特許文献2には、揮発性シリコーンであるM3T(メチルトリメチコン)、不揮発性シリコーン誘導体及びカチオン界面活性剤を組み合わせた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 in which volatile silicone M3T (methyltrimethicone), a nonvolatile silicone derivative and a cationic surfactant are combined.
 また特許文献3には、疎水性シリコーン化合物と親水性シリコーン化合物、並びに各種活性剤やポリマー類を含有し、光学的に透明な毛髪トリートメント剤が開示されている。 Patent Document 3 discloses an optically transparent hair treatment agent containing a hydrophobic silicone compound and a hydrophilic silicone compound, as well as various active agents and polymers.
    (特許文献1)特開平6-172131号公報
    (特許文献2)特開2006-265205号公報
    (特許文献3)特表2008-520614号公報
(Patent Document 1) JP-A-6-172131 (Patent Document 2) JP-A-2006-265205 (Patent Document 3) JP-T 2008-520614
 本発明は、成分(A)~(D)及び水を含有する、毛髪に適用した後洗い流して使用される毛髪化粧料を提供するものである。
 (A) カチオン界面活性剤
 (B) 高級アルコール
 (C) ポリオキシアルキレン側鎖及びアミノアルキル側鎖を有するシリコーン
 (D) 揮発性シリコーン
The present invention provides a hair cosmetic containing components (A) to (D) and water, which is used after being applied to hair and washed away.
(A) Cationic surfactant (B) Higher alcohol (C) Silicone having polyoxyalkylene side chain and aminoalkyl side chain (D) Volatile silicone
 また本発明は、上記の毛髪化粧料を毛髪に塗布し、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-described hair cosmetic is applied to the hair and washed away with water.
発明の詳細な説明Detailed Description of the Invention
 近年、ヘアカラー、パーマ等の化学施術に加え、若年層の女性を中心に習慣化してきているヘアアイロン、ドライヤー等の熱を利用したヘアセットなどによる毛髪のダメージが深刻化している。毛髪ダメージは、毛髪表面を覆う脂肪酸である18-MEA(18-メチルエイコサン酸)の喪失を伴い、毛髪表面の親水化と共に、表面摩擦の増大を引き起こすことが知られている。ダメージを受けて親水化した毛髪は、滑らかさが失われるだけでなく、洗髪した後に乾きにくくなり、ドライヤーなどによる乾燥に長時間要することとなり、体力的負担になっている。また、濡れているダメージ毛は絡まりやすく、ドライヤー乾燥中に生じるひっかかりは更なるダメージの蓄積と消費者の心理的負担になっている。 In recent years, in addition to chemical treatments such as hair coloring and perm, hair damage caused by hair sets using heat such as hair irons and hair dryers, which has become a habit mainly among young women, has become serious. It is known that hair damage is accompanied by the loss of 18-MEA (18-methyleicosanoic acid), which is a fatty acid covering the hair surface, and causes increased surface friction as the hair surface becomes hydrophilic. Damaged and hydrophilized hair not only loses its smoothness but also becomes difficult to dry after shampooing, and it takes a long time to dry with a dryer or the like, which is a physical burden. In addition, wet damaged hair tends to get entangled, and the catches that occur during drying of the dryer add to the accumulation of further damage and the psychological burden on the consumer.
 しかしながら、従来の毛髪処理剤は、毛髪に滑らかさやしっとり感を付与するために、シリコーン類や油剤類を毛髪上に残留させているが、これらが粘着性を有するため毛髪1本1本がばらけることを阻害し、洗髪後の髪を乾かすのに時間がかかるという問題があった。 However, conventional hair treatment agents leave silicones and oils on the hair in order to give the hair a smooth and moist feeling. However, since these have stickiness, each hair is separated. There is a problem that it takes time to dry the hair after washing.
 したがって本発明は、シャンプー洗髪後に髪に適用した後洗い流すことにより、含有するカチオン界面活性剤の種類によらず、濡れた髪1本1本を極めてばらけやすくして、絡まりなく、髪を短時間で乾燥させることができ、しかもすすぎ時の滑らかさに優れる毛髪化粧料に関する。 Therefore, the present invention makes it easy to disperse each piece of wet hair, regardless of the type of cationic surfactant contained, by washing it after applying it to the hair after shampooing. The present invention relates to a hair cosmetic that can be dried over time and has excellent smoothness during rinsing.
 なお、前述の特許文献2には、ヘアコンディショニング組成物を毛髪に塗布した後の乾燥が速いことが記載されている。しかし、当該文献に具体的に開示された乾きの速いヘアコンディショニング組成物は洗い流さないタイプのみであり、当該発明における「塗布後の乾燥が速い」という効果も、ヘアコンディショニング組成物自体の乾燥が速いということである。したがって、当該文献には、毛髪に塗布後、洗い流して十分に濡れた毛髪から、水が乾燥する速さに関してはまったく示唆されていない。 In addition, the above-mentioned patent document 2 describes that drying after applying a hair conditioning composition to hair is quick. However, the fast-drying hair conditioning composition specifically disclosed in the literature is only a type that does not wash away, and the effect of “fast drying after application” in the present invention is also fast drying of the hair conditioning composition itself. That's what it means. Therefore, this document does not suggest at all the speed with which water is dried from hair that has been applied to the hair and then washed away and sufficiently wet.
 洗髪後の髪の乾燥速度を高める因子としては、「髪のばらけ」が重要である。すなわち、髪がばらけることによって、タオルドライ時にはタオルとの接触面積が増大して髪の水分がタオルに速く吸収されることになり、またドライヤー乾燥時には(自然乾燥時にも)空気との接触面積が増大して髪の水分が速く蒸散することになる。 “Hair dispersal” is important as a factor to increase the drying speed of hair after washing. That is, when the hair is dispersed, the contact area with the towel increases when the towel is dried, and moisture of the hair is absorbed quickly by the towel, and when the dryer is dried (even during natural drying), the contact area with the air is increased. Will increase and the moisture of the hair will evaporate quickly.
 本発明者らは、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、特定構造のアミノ・ポリエーテル共変性シリコーンと揮発性シリコーンを併用することによって、毛髪上の粘着成分吸着量が少なくなり、かつ嵩高い粘着成分が毛髪に付着し難くなることを見出した。そしてその結果として、毛髪1本1本の粘着性を弱めることができ、処理後の濡れ髪が極めてばらけやすくなり、絡まりなく乾燥速度を飛躍的に向上させることができることを見出した。 In the hair cosmetics of the type to be used after shampooing, such as hair rinse, hair conditioner, etc., the present inventors have used an amino-polyether co-modified silicone having a specific structure and a volatile silicone in combination to produce an adhesive component on the hair. It has been found that the amount of adsorption is reduced and the bulky adhesive component hardly adheres to the hair. As a result, the present inventors have found that the adhesiveness of each hair can be weakened, wet hair after treatment becomes extremely easy to disperse, and the drying speed can be dramatically improved without tangling.
〔成分(A):カチオン界面活性剤〕
 成分(A)のカチオン界面活性剤としては、例えば、(i)アルキルトリメチルアンモニウム塩、(ii)アルコキシアルキルトリメチルアンモニウム塩、(iii)ジアルキルジメチルアンモニウム塩、(iv)アルキルジメチルアミン及びその塩、(v)アルコキシアルキルジメチルアミン及びその塩、(vi)アルキルアミドアルキルジメチルアミン及びその塩等が挙げられる。
[Component (A): Cationic surfactant]
Examples of the cationic surfactant of component (A) include (i) alkyltrimethylammonium salt, (ii) alkoxyalkyltrimethylammonium salt, (iii) dialkyldimethylammonium salt, (iv) alkyldimethylamine and salts thereof, ( v) alkoxyalkyldimethylamine and its salt, (vi) alkylamidoalkyldimethylamine and its salt, and the like.
(i)アルキルトリメチルアンモニウム塩
 アルキルトリメチルアンモニウム塩としては、例えば下記一般式(1)で表されるものが挙げられる。
  R1-N+(CH3)3  X-    (1)
〔式中、R1は炭素数12~22のアルキル基を示し、X-は塩化物イオン、臭化物イオン等のハロゲン化物イオン;メトサルフェートイオン、エトサルフェートイオン、メトフォスフェートイオン、エトフォスフェートイオン、メトカーボナートイオン等を示す。〕
(I) Alkyltrimethylammonium salt Examples of the alkyltrimethylammonium salt include those represented by the following general formula (1).
R 1 -N + (CH 3) 3 X - (1)
[Wherein R 1 represents an alkyl group having 12 to 22 carbon atoms, and X represents a halide ion such as a chloride ion or a bromide ion; a methosulphate ion, an ethosulphate ion, a methosphosphate ion, an ethosphosphate ion. , Methocarbonate ions and the like. ]
 具体的には、セチルトリメチルアンモニウムクロリド、ステアリルトリメチルアンモニウムクロリド、ベヘニルトリメチルアンモニウムクロリド、ベヘニルトリメチルアンモニウムメトサルフェート等が挙げられる。 Specific examples include cetyltrimethylammonium chloride, stearyltrimethylammonium chloride, behenyltrimethylammonium chloride, behenyltrimethylammonium methosulfate and the like.
(ii)アルコキシアルキルトリメチルアンモニウム塩
 アルコキシアルキルトリメチルアンモニウム塩としては、例えば下記一般式(2)で表されるものが挙げられる。
  R2-O-R3-N+(CH3)3  X-    (2)
〔式中、R2は炭素数12~22のアルキル基を示し、R3はヒドロキシ基が置換していてもよいエチレン基又はプロピレン基を示し、X-は塩化物イオン、臭化物イオン等のハロゲン化物イオン;メトサルフェートイオン、エトサルフェートイオン、メトフォスフェートイオン、エトフォスフェートイオン、メトカーボナートイオン等を示す。〕
(Ii) Alkoxyalkyltrimethylammonium salt Examples of the alkoxyalkyltrimethylammonium salt include those represented by the following general formula (2).
R 2 —O—R 3 —N + (CH 3 ) 3 X (2)
[Wherein R 2 represents an alkyl group having 12 to 22 carbon atoms, R 3 represents an ethylene group or a propylene group optionally substituted by a hydroxy group, and X represents a halogen such as a chloride ion or a bromide ion. Compound ion; methosulphate ion, ethosulphate ion, methosphosphate ion, ethosphosphate ion, methcarbonate ion, etc. ]
 具体的には、ステアロキシプロピルトリメチルアンモニウムクロリド、ステアロキシエチルトリメチルアンモニウムクロリド、ステアロキシヒドロキシプロピルトリメチルアンモニウムクロリド等が挙げられる。 Specific examples include stearoxypropyltrimethylammonium chloride, stearoxyethyltrimethylammonium chloride, stearoxyhydroxypropyltrimethylammonium chloride, and the like.
(iii)ジアルキルジメチルアンモニウム塩
 ジアルキルジメチルアンモニウム塩としては、例えば下記一般式(3)で表されるものが挙げられる。
  (R4)2+(CH3)2  X-    (3)
〔式中、R4はそれぞれ独立して炭素数12~22のアルキル基又はベンジル基を示し、X-は塩化物イオン、臭化物イオン等のハロゲン化物イオン;メトサルフェートイオン、エトサルフェートイオン、メトフォスフェートイオン、エトフォスフェートイオン、メトカーボナートイオン等を示す。〕
(Iii) Dialkyldimethylammonium salt Examples of the dialkyldimethylammonium salt include those represented by the following general formula (3).
(R 4) 2 N + ( CH 3) 2 X - (3)
[Wherein, R 4 independently represents an alkyl group having 12 to 22 carbon atoms or a benzyl group, and X represents a halide ion such as a chloride ion or a bromide ion; a methosulphate ion, an ethosulphate ion, or a methophos ion. Examples of such ions include fate ions, ethophosphate ions, methocarbonate ions, and the like. ]
 具体的には、ジステアリルジメチルアンモニウムクロリド等が挙げられる。 Specific examples include distearyl dimethyl ammonium chloride.
(iv)アルキルジメチルアミン及びその塩
 アルキルジメチルアミンは、酸と反応して4級アンモニウム塩となり、界面活性剤となる。したがって、ここでは、アルキルジメチルアミン及びその塩をカチオン界面活性剤と定義する。また、その含有量は、アルキルジメチルアミンの質量で換算する。アルキルジメチルアミン及びその塩としては、例えば下記一般式(4)で表されるもの及びその塩が挙げられる。
  R5-N(CH3)2    (4)
〔式中、R5は炭素数12~22のアルキル基を示す。〕
(Iv) Alkyldimethylamine and its salt Alkyldimethylamine reacts with an acid to form a quaternary ammonium salt, which becomes a surfactant. Therefore, alkyldimethylamine and its salt are defined here as a cationic surfactant. Moreover, the content is converted by the mass of alkyldimethylamine. Examples of alkyldimethylamine and salts thereof include those represented by the following general formula (4) and salts thereof.
R 5 —N (CH 3 ) 2 (4)
[Wherein R 5 represents an alkyl group having 12 to 22 carbon atoms. ]
 塩としては、有機酸又は無機酸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;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;ポリグルタミン酸等のポリカルボン酸;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;グルタミン酸、アスパラギン酸等の酸性アミノ酸等が挙げられる。無機酸としては、例えば、塩酸、硫酸、リン酸等が挙げられる。これらの中で、有機酸が好ましく、ジカルボン酸、ヒドロキシカルボン酸、酸性アミノ酸が好ましく、ジカルボン酸としてはマレイン酸、コハク酸がより好ましい。ヒドロキシカルボン酸としてはグリコール酸、乳酸、リンゴ酸がより好ましい。酸性アミノ酸としてはグルタミン酸がより好ましい。 Examples of the salt include salts with organic acids or inorganic acids. Examples of the organic acid include monocarboxylic acids such as acetic acid and propionic acid; dicarboxylic acids such as malonic acid, succinic acid, glutaric acid, adipic acid, maleic acid, fumaric acid, and phthalic acid; polycarboxylic acids such as polyglutamic acid; Examples thereof include hydroxycarboxylic acids such as glycolic acid, lactic acid, hydroxyacrylic acid, glyceric acid, malic acid, tartaric acid and citric acid; acidic amino acids such as glutamic acid and aspartic acid. Examples of the inorganic acid include hydrochloric acid, sulfuric acid, phosphoric acid and the like. Among these, organic acids are preferable, dicarboxylic acids, hydroxycarboxylic acids, and acidic amino acids are preferable. As the dicarboxylic acids, maleic acid and succinic acid are more preferable. As the hydroxycarboxylic acid, glycolic acid, lactic acid, and malic acid are more preferable. As the acidic amino acid, glutamic acid is more preferable.
 具体的なアルキルジメチルアミン及びその塩としては、N,N-ジメチルベヘニルアミン、N,N-ジメチルステアリルアミン及びそれらの有機酸塩が挙げられ、N,N-ジメチルベヘニルアミンの乳酸塩、N,N-ジメチルステアリルアミンのグリコール酸塩などが好ましい。 Specific examples of alkyldimethylamine and salts thereof include N, N-dimethylbehenylamine, N, N-dimethylstearylamine, and organic acid salts thereof. N, N-dimethylbehenylamine lactate, N, N-dimethylstearylamine glycolate and the like are preferred.
(v)アルコキシアルキルジメチルアミン及びその塩
 アルコキシアルキルジメチルアミンは、酸と反応して4級アンモニウム塩となり、界面活性剤となる。したがって、ここでは、アルコキシアルキルジメチルアミン及びその塩をカチオン界面活性剤と定義する。また、その含有量は、アルコキシアルキルジメチルアミンの質量で換算する。アルコキシアルキルジメチルアミン及びその塩としては、例えば下記一般式(5)で表されるもの及びその塩が挙げられる。
  R6-O-R7-N(CH3)2    (5)
〔式中、R6は炭素素数12~22のアルキル基を示し、R7はエチレン基又はプロピレン基を示す。〕
(V) Alkoxyalkyldimethylamine and salts thereof Alkoxyalkyldimethylamine reacts with an acid to form a quaternary ammonium salt, which becomes a surfactant. Accordingly, alkoxyalkyldimethylamine and its salts are defined herein as cationic surfactants. Moreover, the content is converted with the mass of alkoxyalkyl dimethylamine. Examples of the alkoxyalkyldimethylamine and salts thereof include those represented by the following general formula (5) and salts thereof.
R 6 —O—R 7 —N (CH 3 ) 2 (5)
[Wherein R 6 represents an alkyl group having 12 to 22 carbon atoms, and R 7 represents an ethylene group or a propylene group. ]
 塩としては、有機酸又は無機酸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;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;ポリグルタミン酸等のポリカルボン酸;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;グルタミン酸、アスパラギン酸等の酸性アミノ酸等が挙げられる。無機酸としては、例えば、塩酸、硫酸、リン酸等が挙げられる。これらの中で、有機酸が好ましく、ジカルボン酸、ヒドロキシカルボン酸、酸性アミノ酸が好ましく、ジカルボン酸としてはマレイン酸、コハク酸がより好ましい。ヒドロキシカルボン酸としてはグリコール酸、乳酸、リンゴ酸がより好ましい。酸性アミノ酸としてはグルタミン酸がより好ましい。 Examples of the salt include salts with organic acids or inorganic acids. Examples of the organic acid include monocarboxylic acids such as acetic acid and propionic acid; dicarboxylic acids such as malonic acid, succinic acid, glutaric acid, adipic acid, maleic acid, fumaric acid, and phthalic acid; polycarboxylic acids such as polyglutamic acid; Examples thereof include hydroxycarboxylic acids such as glycolic acid, lactic acid, hydroxyacrylic acid, glyceric acid, malic acid, tartaric acid and citric acid; acidic amino acids such as glutamic acid and aspartic acid. Examples of the inorganic acid include hydrochloric acid, sulfuric acid, phosphoric acid and the like. Among these, organic acids are preferable, dicarboxylic acids, hydroxycarboxylic acids, and acidic amino acids are preferable. As the dicarboxylic acids, maleic acid and succinic acid are more preferable. As the hydroxycarboxylic acid, glycolic acid, lactic acid, and malic acid are more preferable. As the acidic amino acid, glutamic acid is more preferable.
 具体的なアルコキシアルキルジメチルアミン及びその塩としては、N,N-ジメチル-3-ヘキサデシルオキシプロピルアミン、N,N-ジメチル-3-オクタデシルオキシプロピルアミン及びそれらの有機酸塩が挙げられ、N,N-ジメチル-3-ヘキサデシルオキシプロピルアミンの乳酸塩、N,N-ジメチル-3-オクタデシルオキシプロピルアミンのグリコール酸塩が好ましい。 Specific alkoxyalkyldimethylamines and salts thereof include N, N-dimethyl-3-hexadecyloxypropylamine, N, N-dimethyl-3-octadecyloxypropylamine and organic acid salts thereof, N N, N-dimethyl-3-hexadecyloxypropylamine lactate and N, N-dimethyl-3-octadecyloxypropylamine glycolate are preferred.
(vi)アルキルアミドアルキルジメチルアミン及びその塩
 アルキルアミドアルキルジメチルアミンは、酸と反応して4級アンモニウム塩となり、界面活性剤となる。したがって、ここでは、アルキルアミドアルキルジメチルアミン及びその塩をカチオン界面活性剤と定義する。また、その含有量は、アルキルアミドアルキルジメチルアミンの質量で換算する。アルキルアミドアルキルジメチルアミン及びその塩としては、例えば下記一般式(6)で表されるもの及びその塩が挙げられる。
  R8-CONH-(CH2)m-N(CH3)2    (6)
〔式中、R8は炭素数12~22のアルキル基を示し、mは2~4の数を示す。〕
(vi) Alkylamidoalkyldimethylamine and its salt Alkylamidoalkyldimethylamine reacts with an acid to form a quaternary ammonium salt to become a surfactant. Therefore, herein, alkylamidoalkyldimethylamine and salts thereof are defined as cationic surfactants. Moreover, the content is converted with the mass of alkylamide alkyl dimethylamine. Examples of the alkylamidoalkyldimethylamine and salts thereof include those represented by the following general formula (6) and salts thereof.
R 8 —CONH— (CH 2 ) m —N (CH 3 ) 2 (6)
[Wherein R 8 represents an alkyl group having 12 to 22 carbon atoms, and m represents a number of 2 to 4. ]
 これらの中で、R8が、すすぎ時の滑らかさ、ドライヤー乾燥中の絡まりにくさの観点から、炭素数14~22のアルキル基であるものが好ましく、炭素数16~20のアルキル基であるものがより好ましい。
 塩としては、有機酸又は無機酸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;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;ポリグルタミン酸等のポリカルボン酸;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;グルタミン酸、アスパラギン酸等の酸性アミノ酸等が挙げられる。無機酸としては、例えば、塩酸、硫酸、リン酸等が挙げられる。これらの中で、有機酸が好ましく、ジカルボン酸、ヒドロキシカルボン酸、酸性アミノ酸が好ましく、ジカルボン酸としてはマレイン酸、コハク酸がより好ましい。ヒドロキシカルボン酸としてはグリコール酸、乳酸、リンゴ酸がより好ましい。酸性アミノ酸としてはグルタミン酸がより好ましい。
Among these, R 8 is preferably an alkyl group having 14 to 22 carbon atoms, and preferably an alkyl group having 16 to 20 carbon atoms, from the viewpoint of smoothness during rinsing and difficulty in entanglement during drying of the dryer. Those are more preferred.
Examples of the salt include salts with organic acids or inorganic acids. Examples of the organic acid include monocarboxylic acids such as acetic acid and propionic acid; dicarboxylic acids such as malonic acid, succinic acid, glutaric acid, adipic acid, maleic acid, fumaric acid, and phthalic acid; polycarboxylic acids such as polyglutamic acid; Examples thereof include hydroxycarboxylic acids such as glycolic acid, lactic acid, hydroxyacrylic acid, glyceric acid, malic acid, tartaric acid and citric acid; acidic amino acids such as glutamic acid and aspartic acid. Examples of the inorganic acid include hydrochloric acid, sulfuric acid, phosphoric acid and the like. Among these, organic acids are preferable, dicarboxylic acids, hydroxycarboxylic acids, and acidic amino acids are preferable. As the dicarboxylic acids, maleic acid and succinic acid are more preferable. As the hydroxycarboxylic acid, glycolic acid, lactic acid, and malic acid are more preferable. As the acidic amino acid, glutamic acid is more preferable.
 具体的なアルキルアミドアルキルジメチルアミン及びその塩としては、N-(3-(ジメチルアミノ)プロピル)ドコサナミド及びその塩、N-(3-(ジメチルアミノ)プロピル)ステアラミド及びその塩が挙げられる。 Specific examples of the alkylamidoalkyldimethylamine and salts thereof include N- (3- (dimethylamino) propyl) docosanamide and salts thereof, and N- (3- (dimethylamino) propyl) stearamide and salts thereof.
 これらの中で、(i)アルキルトリメチルアンモニウム塩、(ii)アルコキシアルキルトリメチルアンモニウム塩、(v)アルコキシアルキルジメチルアミン及びその塩、(vi)アルキルアミドアルキルジメチルアミン及びその塩が好ましく、乾燥したと感じるまでの時間の短さの観点から、(v)アルコキシアルキルジメチルアミン及びその塩、(vi)アルキルアミドアルキルジメチルアミン及びその塩が好ましい。更には、すすぎ時の滑らかさ、毛束のばらけやすさ、ドライヤー乾燥中の絡まりにくさ、及び乾燥の速さの観点から、N,N-ジメチル-3-ヘキサデシルオキシプロピルアミン及びその塩、N,N-ジメチル-3-オクタデシルオキシプロピルアミン及びその塩、N-(3-(ジメチルアミノ)プロピル)ドコサナミド及びその塩、N-(3-(ジメチルアミノ)プロピル)ステアラミド及びその塩が好ましい。 Among these, (i) alkyltrimethylammonium salt, (ii) alkoxyalkyltrimethylammonium salt, (v) alkoxyalkyldimethylamine and salt thereof, (vi) alkylamidoalkyldimethylamine and salt thereof are preferable, and dried. From the viewpoint of short time to feel, (v) alkoxyalkyldimethylamine and its salt, and (vi) alkylamidoalkyldimethylamine and its salt are preferable. Furthermore, N, N-dimethyl-3-hexadecyloxypropylamine and its salts are considered from the viewpoints of smoothness during rinsing, ease of hair bundling, difficulty in entanglement during dryer drying, and speed of drying. N, N-dimethyl-3-octadecyloxypropylamine and its salt, N- (3- (dimethylamino) propyl) docosanamide and its salt, N- (3- (dimethylamino) propyl) stearamide and its salt are preferable .
 成分(A)のカチオン界面活性剤は、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。本発明の毛髪化粧料における成分(A)の含有量は、コンディショナー使用時の滑らかさと適切な速乾性能の観点から、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0.75質量%以上であり、また、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、更に好ましくは4質量%以下、更に好ましくは3質量%以下である。 Component (A) cationic surfactant can be used alone or in combination of two or more. The content of the component (A) in the hair cosmetic composition of the present invention is preferably 0.1% by mass or more, more preferably 0.5% by mass or more, and still more preferably 0.75% from the viewpoint of smoothness when using a conditioner and appropriate quick drying performance. It is preferably 10% by mass or less, more preferably 8% by mass or less, still more preferably 6% by mass or less, still more preferably 4% by mass or less, and further preferably 3% by mass or less.
〔成分(B):高級アルコール〕
 成分(B)の高級アルコールとしては、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、その炭素数は、好ましくは10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、また、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。具体的に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。これらのうち、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い。これらの高級アルコールは、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。
[Component (B): Higher alcohol]
The higher alcohol of component (B) may be linear and branched, or saturated and unsaturated aliphatic alcohols, and the carbon number thereof is preferably 10 or more, more preferably 14 or more, and still more preferably 16 In addition, it is preferably 22 or less, more preferably 20 or less, and still more preferably 18 or less. Specific examples include lauryl alcohol, myristyl alcohol, cetyl alcohol, stearyl alcohol, aralkyl alcohol, hexyl decanol, isostearyl alcohol, oleyl alcohol, 2-octyldodecanol and the like. Of these, stearyl alcohol, cetyl alcohol, and myristyl alcohol are preferred. These higher alcohols can be used alone or in combination of two or more.
 本発明の毛髪化粧料における成分(B)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、好ましくは1質量%以上、より好ましくは2質量%以上、更に好ましくは3質量%以上であり、また、速乾性能、乾燥後のべたつき抑制、及び使いやすい粘度に調整する観点から、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7質量%以下、更に好ましくは6質量%以下である。 The content of the component (B) in the hair cosmetic composition of the present invention is preferably 1% by mass or more, more preferably 2% by mass or more, and further preferably 3% from the viewpoint of smoothness from application to rinsing and after drying. From the viewpoint of quick drying performance, stickiness control after drying, and adjustment to an easy-to-use viscosity, it is preferably 10% by mass or less, more preferably 8% by mass or less, and even more preferably 7% by mass or less. More preferably, it is 6 mass% or less.
〔成分(C):ポリオキシアルキレン側鎖及びアミノアルキル側鎖を有するシリコーン〕
 成分(C)のポリオキシアルキレン側鎖及びアミノアルキル側鎖を有するシリコーンとしては、例えば、下記一般式(7)で表されるものが挙げられる。
[Component (C): Silicone having polyoxyalkylene side chain and aminoalkyl side chain]
Examples of the silicone having a polyoxyalkylene side chain and an aminoalkyl side chain as component (C) include those represented by the following general formula (7).
Figure JPOXMLDOC01-appb-C000003
Figure JPOXMLDOC01-appb-C000003
〔式中、rは1~50の整数、sは1~50の整数、tは1~50の整数、aは0~50の整数、bは0~50を示し(aとbとが同時に0になることはない)、カッコ内の各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。R9は炭素数1~6の2価の炭化水素基を示し、R10は-R11Zで表されるアミノ基又はアンモニウム基を有する置換基を示す。ここで、R11は炭素数1~6の2価の炭化水素基を示し、Zは-NR12 2、-NR12(CH2)cNR12 2、及び-NR12(CH2)cNR12C=O(R13)からなる群より選ばれる1価の基を示し、R12は水素原子又は炭素数1~4の炭化水素基を示し、R13は炭素数1~4の炭化水素基を示し、cは2~6の整数を示し、R14は炭素数1~4の炭化水素基又はトリメチルシリル基を示す。〕 [Wherein, r is an integer of 1 to 50, s is an integer of 1 to 50, t is an integer of 1 to 50, a is an integer of 0 to 50, b is 0 to 50 (a and b are simultaneously (It is never 0), and the bonding order of the structural units in the parenthesis is not limited, and the bonding form may be block or random. R 9 represents a divalent hydrocarbon group having 1 to 6 carbon atoms, and R 10 represents a substituent having an amino group or an ammonium group represented by —R 11 Z. Here, R 11 represents a divalent hydrocarbon group having 1 to 6 carbon atoms, and Z represents —NR 12 2 , —NR 12 (CH 2 ) c NR 12 2 , and —NR 12 (CH 2 ) c NR 12 represents a monovalent group selected from the group consisting of C═O (R 13 ), R 12 represents a hydrogen atom or a hydrocarbon group having 1 to 4 carbon atoms, and R 13 represents a hydrocarbon having 1 to 4 carbon atoms. C represents an integer of 2 to 6, and R 14 represents a hydrocarbon group having 1 to 4 carbon atoms or a trimethylsilyl group. ]
 これらの中で、R9が炭素数2~4の2価の炭化水素基、R10が-R11-NH2、R11が炭素数2~4の2価の炭化水素基、R12及びR14が各々独立にメチル基又はエチル基であるものが好ましい。 Among these, R 9 is a divalent hydrocarbon group having 2 to 4 carbon atoms, R 10 is —R 11 —NH 2 , R 11 is a divalent hydrocarbon group having 2 to 4 carbon atoms, R 12 and It is preferable that each R 14 is independently a methyl group or an ethyl group.
 成分(C)の25℃における粘度は、濡れた髪1本1本を極めてばらけやすくし、指通りを向上させ、しかもすすぎ時の滑らかさに優れるものとする観点から、好ましくは4000mm2/s以下、より好ましくは3000mm2/s以下、更に好ましくは2000mm2/s以下、更に好ましくは1000mm2/s以下、更に好ましくは800mm2/s以下であり、また、好ましくは100mm2/s以上、より好ましくは200mm2/s以上である。 The viscosity at 25 ° C. of component (C), a single one hair wet very loose and easy to improve the finger combability, yet from the viewpoint of the excellent in smoothness during rinsing, preferably 4000 mm 2 / s or less, more preferably 3000 mm 2 / s or less, further preferably 2000 mm 2 / s or less, more preferably 1000 mm 2 / s or less, more preferably 800 mm 2 / s or less, and preferably 100 mm 2 / s or more. More preferably, it is 200 mm 2 / s or more.
 なお、25℃での粘度は、毛細管式粘度計を使って、一定容量の液体が25℃、1013.25hPa下で粘度計の毛細管を流れる時間を測定し、この流出時間と粘度計定数から次式を用いて算出される。毛細管式粘度計は、一般にウベローデやキャノン-フェンスケなどの型式が用いられる。 The viscosity at 25 ° C was measured using a capillary viscometer, and the time for a certain volume of liquid to flow through the capillary of the viscometer at 25 ° C and 1013.25 hPa was measured. Is calculated using The capillary viscometer is generally of a type such as Ubbelohde or Canon-Fenske.
<粘度の算出方法>
  粘度(mm2/s)=流出時間(秒)×粘度計定数
<Viscosity calculation method>
Viscosity (mm 2 / s) = Outflow time (seconds) x Viscometer constant
 成分(C)の具体例としては、ABIL SOFT AF100(エヴォニック インダストリー社製:粘度400mm2/s)、X-22-3939A(信越化学工業社製:粘度2,800mm2/s)、Silsense A21(ルブリゾール社製:粘度250mm2/s)等が挙げられる。 Specific examples of component (C) include ABIL SOFT AF100 (Evonik Industry Co., Ltd .: viscosity 400 mm 2 / s), X-22-3939A (Shin-Etsu Chemical Co., Ltd .: viscosity 2,800 mm 2 / s), Silsense A21 (Lubrisol) (Manufactured by company: viscosity 250 mm 2 / s).
 成分(C)のポリオキシアルキレン側鎖及びアミノアルキル側鎖を有するシリコーンは、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。本発明の毛髪化粧料における成分(C)の含有量は、濡れた髪をばらけやすくして、絡まりなく、髪を短時間で乾燥させる観点から、好ましくは0.05質量%以上、より好ましくは0.1質量%以上、更に好ましくは0.2質量%以上、更に好ましくは0.3質量%以上であり、また、すすぎ時の滑らかさ、乾燥中の絡まりにくさ、速乾性能、乾燥後のべたつき抑制、及び使いやすい粘度への調整の観点から、好ましくは5質量%以下、より好ましくは4質量%以下、更に好ましくは3質量%以下、更に好ましくは2.5質量%以下である。 As the component (C), the silicone having a polyoxyalkylene side chain and an aminoalkyl side chain can be used alone or in combination of two or more. The content of the component (C) in the hair cosmetic composition of the present invention is preferably 0.05% by mass or more, more preferably 0.1%, from the viewpoint of easily spreading wet hair, preventing tangling, and drying the hair in a short time. % By mass or more, more preferably 0.2% by mass or more, more preferably 0.3% by mass or more. Also, smoothness during rinsing, difficulty in entanglement during drying, quick drying performance, suppression of stickiness after drying, and ease of use From the viewpoint of adjusting the viscosity, it is preferably 5% by mass or less, more preferably 4% by mass or less, still more preferably 3% by mass or less, and further preferably 2.5% by mass or less.
〔成分(D):揮発性シリコーン〕
 成分(D)の揮発性シリコーンとしては、1013.25hPa下における沸点が260℃以下の鎖状及び環状のシリコーン油からなる群より選択される1種又は2種以上を用いることができる。また、保存時の安定性の観点から1013.25hPa下における沸点が35℃以上であることが好ましい。
[Component (D): Volatile silicone]
As the volatile silicone of component (D), one or more selected from the group consisting of linear and cyclic silicone oils having a boiling point of 260 ° C. or lower under 1013.25 hPa can be used. Further, from the viewpoint of stability during storage, the boiling point under 1013.25 hPa is preferably 35 ° C. or higher.
 鎖状の揮発性シリコーンとしては、例えば下記式(8)又は下記一般式(9)で表される鎖状シリコーンが挙げられ、環状の揮発性シリコーンとしては、例えば下記一般式(10)で表される環状シリコーンが挙げられる。 Examples of the chain volatile silicone include chain silicones represented by the following formula (8) or the following general formula (9), and examples of the cyclic volatile silicone include those represented by the following general formula (10). And cyclic silicone.
Figure JPOXMLDOC01-appb-C000004
Figure JPOXMLDOC01-appb-C000004
Figure JPOXMLDOC01-appb-C000005
Figure JPOXMLDOC01-appb-C000005
Figure JPOXMLDOC01-appb-C000006
Figure JPOXMLDOC01-appb-C000006
 このうち、濡れた髪1本1本を極めてばらけやすくし、指通りを向上させ、しかもすすぎ時の滑らかさに優れるものとする観点から、式(8)で表されるメチルトリメチコンが好ましい。 Among these, methyltrimethicone represented by the formula (8) is preferable from the viewpoint of making each wet hair very easy to disperse, improving finger passage, and excellent smoothness during rinsing. .
 成分(D)の揮発性シリコーンは、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。本発明の毛髪化粧料における成分(D)の含有量は、濡れた髪をばらけやすくして、絡まりなく、髪を短時間で乾燥させる観点から、好ましくは0.05質量%以上、より好ましくは0.1質量%以上、更に好ましくは0.5質量%以上であり、また、毛髪のばらけやすさ、乾燥の速さ、すすぎ時のきしみ抑制、及び乾燥後のべたつき抑制の観点から、好ましくは10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、更に好ましくは4質量%以下、更に好ましくは3質量%以下、更に好ましくは2質量%以下である。 The volatile silicone of component (D) can be used alone or in combination of two or more. The content of the component (D) in the hair cosmetic composition of the present invention is preferably 0.05% by mass or more, more preferably 0.1%, from the viewpoint of making it easy to disperse wet hair, preventing tangling, and drying the hair in a short time. It is preferably 10% by mass or less, more preferably 0.5% by mass or more, and from the viewpoint of ease of hair dispersion, speed of drying, suppression of squeezing during rinsing, and suppression of stickiness after drying. More preferably, it is 8 mass% or less, More preferably, it is 6 mass% or less, More preferably, it is 4 mass% or less, More preferably, it is 3 mass% or less, More preferably, it is 2 mass% or less.
 また、成分(D)に対する成分(C)の質量比(C)/(D)は、コンディショニング成分を毛髪表面全体に均一に吸着させ、毛髪1本1本の粘着性を弱めることができ、処理後の濡れ髪を極めてばらけやすくして、絡まりなく乾燥速度を飛躍的に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0.08以上、更に好ましくは0.1以上、更に好ましくは0.2以上であり、また、好ましくは5以下、より好ましくは4以下、更に好ましくは3以下、更に好ましくは2以下、更に好ましくは1以下、更に好ましくは0.8以下である。 In addition, the mass ratio (C) / (D) of component (C) to component (D) allows the conditioning component to be evenly adsorbed to the entire hair surface and weakens the adhesiveness of each hair. From the viewpoint of making the later wet hair very easy to disperse and dramatically improving the drying speed without entanglement, it is preferably 0.01 or more, more preferably 0.05 or more, further preferably 0.08 or more, more preferably 0.1 or more, still more preferably. Is 0.2 or more, preferably 5 or less, more preferably 4 or less, still more preferably 3 or less, still more preferably 2 or less, still more preferably 1 or less, still more preferably 0.8 or less.
〔水〕
 本発明の毛髪化粧料は、媒体として水を含有する。水は、成分(A)~(D)及びその他の成分の残量となる。
〔water〕
The hair cosmetic composition of the present invention contains water as a medium. Water is the remaining amount of components (A) to (D) and other components.
〔その他の任意成分〕
 本発明の毛髪化粧料には更に、毛髪化粧料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、ジメチルポリシロキサン、環状シリコーン、アミノ変性シリコーン、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(C)及び(D)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、イソステアリル酸、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、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、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 hair cosmetic of the present invention may further contain other components generally used in hair cosmetics depending on the purpose. For example, dimethylpolysiloxane, cyclic silicone, amino modified 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, Silicones other than components (C) and (D) such as alkyl-modified silicone; polymer compounds such as cationized 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, sucrose fatty acid ester, polyglycerin alkyl Nonionic surfactants such as ethers, fatty acid alkanolamides, alkylglycosides; hydrocarbons such as squalene, squalane, liquid paraffin, liquid isoparaffin, cycloparaffin; glycerides such as castor oil, cocoa oil, mink oil, avocado oil, olive oil Waxes such as beeswax, spermaceti, lanolin, carnauba wax; isopropyl palmitate, isopropyl myristate, octyldodecyl myristate, hexyl laurate, cetyl lactate, propylene glycol monostearate, oleyl oleate, hexadecyl 2-ethylhexanoate , Esters such as isononyl isononanoate, tridecyl isononanoate; capric acid, lauric acid, myristic acid, palmitic acid, stearic acid, behenic acid, oleic acid, coconut oil fatty acid, lanoli Higher fatty acids such as difatty acid, isostearyl acid and isopalmitic acid; oils such as isostearyl glyceryl ether and polyoxypropylene butyl ether; ethanol, 1-propanol, 2-propanol, butanol, ethylene glycol, propylene glycol, benzyl alcohol, phenoxyethanol Alcohols such as 2-benzyloxyethanol, methyl carbitol, ethyl carbitol, propyl carbitol, butyl carbitol, triethylene glycol monoethyl ether, triethylene glycol monobutyl ether, glycerin; zinc pyrithione, benzalkonium chloride, etc. Antidandruff agent; pH adjuster; vitamin agent; bactericidal agent; anti-inflammatory agent; antiseptic agent; chelating agent; moisturizer such as panthenol; colorant such as dye and pigment; Polar solvent extract, protein obtained from shells or pearls having a pearl layer or hydrolyzate thereof, protein obtained from silk or hydrolyzate thereof, protein-containing extract obtained from legume seeds, ginseng extract, Extracts such as rice germ extract, hibamata extract, camellia extract, aloe extract, moon peach leaf extract, chlorella extract; pearl powder such as mica titanium; refreshing agent such as menthol: fragrance; pigment; UV absorption Agents; antioxidants; and other components described in ENCYCLOPEDIA OF SHAMPOO INGREDIENTS (MICELLE PRESS).
〔pH〕
 本発明の毛髪化粧料のpHは、2.0以上が好ましく、更には2.5以上が好ましく、また7.5以下が好ましく、更には6.5以下、更には5.5以下が好ましい。なお、本発明において、毛髪化粧料のpHは、水で20質量倍希釈したときの25℃における値をいう。
[PH]
The pH of the hair cosmetic composition of the present invention is preferably 2.0 or more, more preferably 2.5 or more, and preferably 7.5 or less, more preferably 6.5 or less, and further preferably 5.5 or less. In the present invention, the pH of the hair cosmetic refers to a value at 25 ° C. when diluted 20 times by weight with water.
 また本発明の毛髪化粧料は、髪に適用後、洗い流して使用されるものであり、例えば、ヘアリンス、ヘアコンディショナー、ヘアトリートメント、ヘアパック等の浴室内で使用されるものが挙げられる。 Further, the hair cosmetic composition of the present invention is used after being applied to the hair and washed away, and examples thereof include those used in the bathroom such as hair rinse, hair conditioner, hair treatment, hair pack and the like.
 本発明の毛髪化粧料を用いて髪のコンディショニング処理を行うには、本発明の毛髪化粧料を髪に塗布した後、水で洗い流せばよい。これにより、すすぎ時の滑らかさに優れ、かつ濡れた髪1本1本を極めてばらけやすくして、絡まりなく指通り良く、髪を短時間で乾燥させることができる。 In order to condition the hair using the hair cosmetic composition of the present invention, the hair cosmetic composition of the present invention is applied to the hair and then washed away with water. Thereby, it is excellent in the smoothness at the time of a rinse, and makes it easy to disperse each wet hair one by one, it is good to pass through a finger without entanglement, and hair can be dried in a short time.
 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 respect to the embodiments described above, preferred embodiments of the present invention will be further disclosed below.
<1> 成分(A)~(D)及び水を含有する、毛髪に適用した後洗い流して使用される毛髪化粧料。
 (A) カチオン界面活性剤
 (B) 高級アルコール
 (C) ポリオキシアルキレン側鎖及びアミノアルキル側鎖を有するシリコーン
 (D) 揮発性シリコーン
<1> A hair cosmetic comprising components (A) to (D) and water, which is used after being applied to hair and washed away.
(A) Cationic surfactant (B) Higher alcohol (C) Silicone having polyoxyalkylene side chain and aminoalkyl side chain (D) Volatile silicone
<2> 成分(A)が、好ましくはアルキルトリメチルアンモニウム塩、アルコキシアルキルトリメチルアンモニウム塩、ジアルキルジメチルアンモニウム塩、アルキルジメチルアミン及びその塩、アルコキシアルキルジメチルアミン及びその塩、並びにアルキルアミドアルキルジメチルアミン及びその塩からなる群より選ばれる1種又は2種以上の化合物である<1>に記載の毛髪化粧料。 <2> Component (A) is preferably alkyltrimethylammonium salt, alkoxyalkyltrimethylammonium salt, dialkyldimethylammonium salt, alkyldimethylamine and its salt, alkoxyalkyldimethylamine and its salt, and alkylamidoalkyldimethylamine and its Hair cosmetic according to <1>, which is one or more compounds selected from the group consisting of salts.
<3> 成分(A)の含有量が、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0.75質量%以上であり、また、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、更に好ましくは4質量%以下、更に好ましくは3質量%以下である<1>又は<2>に記載の毛髪化粧料。 <3> The content of component (A) is preferably 0.1% by mass or more, more preferably 0.5% by mass or more, still more preferably 0.75% by mass or more, and preferably 10% by mass or less, more preferably 8% by mass. The hair cosmetic composition according to <1> or <2>, which is not more than mass%, more preferably not more than 6 mass%, still more preferably not more than 4 mass%, still more preferably not more than 3 mass%.
<4> 成分(B)が、好ましくは炭素数10以上、より好ましくは炭素数14以上、更に好ましくは炭素数16以上の、また、好ましくは炭素数22以下、より好ましくは炭素数20以下、更に好ましくは炭素数18以下の、直鎖又は分岐鎖の飽和又は不飽和の脂肪族アルコールである<1>~<3>のいずれか1項に記載の毛髪化粧料。 <4> Component (B) is preferably 10 or more carbon atoms, more preferably 14 or more carbon atoms, still more preferably 16 or more carbon atoms, and preferably 22 or less carbon atoms, more preferably 20 or less carbon atoms, The hair cosmetic according to any one of <1> to <3>, which is more preferably a linear or branched saturated or unsaturated aliphatic alcohol having 18 or less carbon atoms.
<5> 成分(B)の含有量が、好ましくは1質量%以上、より好ましくは2質量%以上、更に好ましくは3質量%以上であり、また、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7質量%以下、更に好ましくは6質量%以下である<1>~<4>のいずれか1項に記載の毛髪化粧料。 <5> The content of component (B) is preferably 1% by mass or more, more preferably 2% by mass or more, still more preferably 3% by mass or more, and preferably 10% by mass or less, more preferably 8% by mass. The hair cosmetic according to any one of <1> to <4>, which is not more than mass%, more preferably not more than 7 mass%, still more preferably not more than 6 mass%.
<6> 成分(C)が、好ましくは下記一般式(7)で表されるものである<1>~<5>のいずれか1項に記載の毛髪化粧料。 <6> The hair cosmetic according to any one of <1> to <5>, wherein the component (C) is preferably represented by the following general formula (7).
Figure JPOXMLDOC01-appb-C000007
Figure JPOXMLDOC01-appb-C000007
〔式中、rは1~50の整数、sは1~50の整数、tは1~50の整数、aは0~50の整数、bは0~50を示し(aとbとが同時に0になることはない)、カッコ内の各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。R9は炭素数1~6の2価の炭化水素基を示し、R10は-R11Zで表されるアミノ基又はアンモニウム基を有する置換基を示す。ここで、R11は炭素数1~6の2価の炭化水素基を示し、Zは-NR12 2、-NR12(CH2)cNR12 2、及び-NR12(CH2)cNR12C=O(R13)からなる群より選ばれる1価の基を示し、R12は水素原子又は炭素数1~4の炭化水素基を示し、R13は炭素数1~4の炭化水素基を示し、cは2~6の整数を示し、R14は炭素数1~4の炭化水素基又はトリメチルシリル基を示す。〕 [Wherein, r is an integer of 1 to 50, s is an integer of 1 to 50, t is an integer of 1 to 50, a is an integer of 0 to 50, b is 0 to 50 (a and b are simultaneously (It is never 0), and the bonding order of the structural units in the parenthesis is not limited, and the bonding form may be block or random. R 9 represents a divalent hydrocarbon group having 1 to 6 carbon atoms, and R 10 represents a substituent having an amino group or an ammonium group represented by —R 11 Z. Here, R 11 represents a divalent hydrocarbon group having 1 to 6 carbon atoms, and Z represents —NR 12 2 , —NR 12 (CH 2 ) c NR 12 2 , and —NR 12 (CH 2 ) c NR 12 represents a monovalent group selected from the group consisting of C═O (R 13 ), R 12 represents a hydrogen atom or a hydrocarbon group having 1 to 4 carbon atoms, and R 13 represents a hydrocarbon having 1 to 4 carbon atoms. C represents an integer of 2 to 6, and R 14 represents a hydrocarbon group having 1 to 4 carbon atoms or a trimethylsilyl group. ]
<7> 成分(C)の25℃における粘度が、好ましくは4000mm2/s以下、より好ましくは3000mm2/s以下、更に好ましくは2000mm2/s以下、更に好ましくは1000mm2/s以下、更に好ましくは800mm2/s以下であり、また、好ましくは100mm2/s以上、より好ましくは200mm2/s以上であるである<1>~<6>のいずれか1項に記載の毛髪化粧料。 <7> The viscosity of component (C) at 25 ° C. is preferably 4000 mm 2 / s or less, more preferably 3000 mm 2 / s or less, still more preferably 2000 mm 2 / s or less, more preferably 1000 mm 2 / s or less, The hair cosmetic according to any one of <1> to <6>, which is preferably 800 mm 2 / s or less, preferably 100 mm 2 / s or more, more preferably 200 mm 2 / s or more. .
<8> 成分(C)の含有量が、好ましくは0.05質量%以上、より好ましくは0.1質量%以上、更に好ましくは0.2質量%以上、更に好ましくは0.3質量%以上であり、また、好ましくは5質量%以下、より好ましくは4質量%以下、更に好ましくは3質量%以下、更に好ましくは2.5質量%以下である<1>~<7>のいずれか1項に記載の毛髪化粧料。 <8> The content of component (C) is preferably 0.05% by mass or more, more preferably 0.1% by mass or more, still more preferably 0.2% by mass or more, further preferably 0.3% by mass or more, and preferably 5%. The hair cosmetic composition according to any one of <1> to <7>, which is not more than mass%, more preferably not more than 4 mass%, still more preferably not more than 3 mass%, still more preferably not more than 2.5 mass%.
<9> 成分(D)が、好ましくは1013.25hPa下における沸点が260℃以下の鎖状及び環状のシリコーン油からなる群より選択される1種又は2種以上である<1>~<8>のいずれか1項に記載の毛髪化粧料。 <9> Component (D) is preferably one or more selected from the group consisting of linear and cyclic silicone oils having a boiling point of 260 ° C. or lower under 1013.25 hPa <1> to <8> The hair cosmetic composition according to any one of the above.
<10> 成分(D)が、好ましくは式(8)で表される鎖状シリコーン、一般式(9)で表される鎖状シリコーン、及び一般式(10)で表される環状シリコーンからなる群より選ばれる1種又は2種以上の揮発性シリコーンである<9>に記載の毛髪化粧料。 <10> Component (D) preferably comprises a chain silicone represented by formula (8), a chain silicone represented by formula (9), and a cyclic silicone represented by formula (10) Hair cosmetic according to <9>, which is one or more volatile silicones selected from the group.
Figure JPOXMLDOC01-appb-C000008
Figure JPOXMLDOC01-appb-C000008
Figure JPOXMLDOC01-appb-C000009
Figure JPOXMLDOC01-appb-C000009
Figure JPOXMLDOC01-appb-C000010
Figure JPOXMLDOC01-appb-C000010
<11> 成分(D)の含有量が、好ましくは0.05質量%以上、より好ましくは0.1質量%以上、更に好ましくは0.5質量%以上であり、また、好ましくは10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、更に好ましくは4質量%以下、更に好ましくは3質量%以下、更に好ましくは2質量%以下である<1>~<10>のいずれか1項に記載の毛髪化粧料。 <11> The content of component (D) is preferably 0.05% by mass or more, more preferably 0.1% by mass or more, still more preferably 0.5% by mass or more, and preferably 10% by mass or less, more preferably 8% by mass. <1> to <10>, which is not more than mass%, more preferably not more than 6 mass%, still more preferably not more than 4 mass%, still more preferably not more than 3 mass%, still more preferably not more than 2 mass%. The hair cosmetic composition described.
<12> 成分(D)に対する成分(C)の質量比(C)/(D)が、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0.08以上、更に好ましくは0.1以上、更に好ましくは0.2以上であり、また、好ましくは5以下、より好ましくは4以下、更に好ましくは3以下、更に好ましくは2以下、更に好ましくは1以下、更に好ましくは0.8以下である<1>~<11>のいずれか1項に記載の毛髪化粧料。 <12> The mass ratio (C) / (D) of the component (C) to the component (D) is preferably 0.01 or more, more preferably 0.05 or more, still more preferably 0.08 or more, still more preferably 0.1 or more, and still more preferably. It is 0.2 or more, preferably 5 or less, more preferably 4 or less, further preferably 3 or less, further preferably 2 or less, still more preferably 1 or less, and further preferably 0.8 or less. <1> to <11> The hair cosmetic composition according to any one of the above.
<13> 水で20質量倍希釈したときの25℃におけるpHが、好ましくは2.0以上、より好ましくは2.5以上であり、また好ましくは7.5以下、より好ましくは6.5以下、更に好ましくは5.5以下である<1>~<12>のいずれか1項に記載の毛髪化粧料。 <13> The pH at 25 ° C. when diluted 20 times by mass with water is preferably 2.0 or more, more preferably 2.5 or more, preferably 7.5 or less, more preferably 6.5 or less, and even more preferably 5.5 or less. The hair cosmetic according to any one of <1> to <12>.
<14> <1>~<13>のいずれか1項に記載の毛髪化粧料を毛髪に塗布し、水で洗い流す毛髪処理方法。 <14> A hair treatment method in which the hair cosmetic composition according to any one of <1> to <13> is applied to hair and washed away with water.
実施例1~11及び比較例1~3
 表1に示すヘアコンディショナーを調製し、以下の方法及び基準にしたがって、官能評価及び乾燥の速さの測定を行った。
Examples 1 to 11 and Comparative Examples 1 to 3
Hair conditioners shown in Table 1 were prepared, and sensory evaluation and drying speed were measured according to the following methods and standards.
(評価用トレスの作製方法)
 長さ40cm、乾燥時重量20gの毛髪を用いて作製した日本人毛トレスに対し、市販のブリーチ剤(花王社製、泡カラーハイブリーチ)でブリーチ処理(毛髪の5質量倍のブリーチ剤を塗布し、30分間室温で処理)を2回行い、プレーンシャンプーで2回洗浄処理したものを以下の評価に用いた。
 プレーンシャンプー(pH7.0)の組成は以下のとおりである。
25%ポリオキシエチレン(2.5)ラウリルエーテル硫酸ナトリウム塩 62質量%
ラウリン酸ジエタノールアミド                2.3質量%
エデト酸二ナトリウム                    0.15質量%
安息香酸ナトリウム                     0.5質量%
塩化ナトリウム                       0.8質量%
75%リン酸                          適量
香料、メチルパラベン                     微量
精製水                            残量
 合計                           100質量%
(Production method of evaluation tress)
Japanese hair tresses made with hair 40cm long and 20g dry weight are bleached with a commercial bleaching agent (Kao Co., Ltd., Bubble Color Hybrid) and 5 times the mass of hair is applied. And treated for 30 minutes at room temperature) and washed twice with plain shampoo was used for the following evaluation.
The composition of plain shampoo (pH 7.0) is as follows.
25% polyoxyethylene (2.5) lauryl ether sulfate sodium salt 62% by mass
Lauric acid diethanolamide 2.3% by mass
Edetate disodium 0.15% by mass
Sodium benzoate 0.5% by mass
Sodium chloride 0.8 mass%
75% phosphoric acid appropriate amount fragrance, methylparaben trace amount purified water remaining amount total 100% by mass
(官能評価)
「すすぎ時の滑らかさ」
 上記方法で作製した評価用トレスをプレーンシャンプーで洗浄後、軽く水気を取り、表1に記載のコンディショナー1gを塗布し、水道水ですすいだ際の「滑らかさ」について研究員5名で官能評価を実施した。評価は以下の5段階で行い、5名の合計点を算出した。
 5:とても滑らか
 4:滑らか
 3:どちらともいえない
 2:あまり滑らかでない
 1:滑らかでない
(sensory evaluation)
"Smoothness when rinsing"
After washing the evaluation tress made by the above method with a plain shampoo, lightly drain it, apply 1g of the conditioner shown in Table 1, and perform sensory evaluation with 5 researchers on the "smoothness" when rinsed with tap water. Carried out. Evaluation was performed in the following five stages, and the total score of five people was calculated.
5: Very smooth 4: Smooth 3: Not good 2: Not very smooth 1: Not smooth
「毛束のばらけやすさ」
 上記「すすぎ時の滑らかさ」の評価後、当該評価に用いたトレスの含水量が10gとなるように調整した。次いでトレスの上下に、ペーパータオル(大王製紙社製、エリエールプロワイプ)、アクリル板、錘(アクリル板と錘の総重量1.3kg)を順に乗せ、余分な水分を除去した。そのトレスに指を通したときの毛束のほぐれやすさ、小さい毛束の出来やすさを「毛束のばらけやすさ」とし、研究員5名で官能評価を実施した。評価は以下の5段階で行い、5名の合計点を算出した。
 5:とてもばらけやすい
 4:ばらけやすい
 3:どちらともいえない
 2:ややばらけにくい
 1:ばらけにくい
“Ease of hair bundles”
After the evaluation of the “smoothness during rinsing”, the moisture content of the tress used for the evaluation was adjusted to 10 g. Next, a paper towel (manufactured by Daio Paper Co., Ltd., Eliere Pro Wipe), an acrylic plate, and a weight (total weight of acrylic plate and weight 1.3 kg) were placed on the top and bottom of the tres in this order to remove excess water. The ease of loosening of the hair bundle when the finger was passed through the tress and the ease of producing a small hair bundle was defined as “Ease of dispersal of the hair bundle”, and sensory evaluation was conducted by five researchers. Evaluation was performed in the following five stages, and the total score of five people was calculated.
5: Very easy to disperse 4: Easy to disperse 3: Not to say 2: Slightly difficult to disperse 1: Difficult to disperse
「ドライヤー乾燥中の絡まりにくさ」
 上記「毛束のばらけやすさ」の評価後、当該評価に用いたトレスを下向きに設置し、ドライヤー(National社製、TURBODRY1300)の吹き出し口から毛髪トレスの毛髪中心部までの距離が25cmで、温風が約45°斜め上から当たるようにドライヤーを固定した。次いで、4秒に1回ずつトレスに指を通しながらドライヤー乾燥を行った。この際、完全に乾燥するまでの「絡まりにくさ」について研究員5名で官能評価を行った。評価は以下の5段階で行い、5名の合計点を算出した。
 5:絡まらない
 4:ほとんど絡まらない
 3:どちらでもない
 2:やや絡まりやすい
 1:絡まりやすい
"Difficult to get tangled during dryer drying"
After evaluating the above “Ease of dispersal of hair bundles”, install the tresses used for the evaluation downward, and the distance from the outlet of the dryer (National, TURBODRY1300) to the hair center of the hair tress is 25 cm. The dryer was fixed so that the warm air hits from about 45 ° diagonally. Next, the dryer was dried once every 4 seconds while passing the finger through the tress. At this time, sensory evaluation was performed by five researchers on “hardness of entanglement” until it was completely dried. Evaluation was performed in the following five stages, and the total score of five people was calculated.
5: Not entangled 4: Almost entangled 3: Neither of them 2: Slightly entangled 1: Slightly entangled
(乾燥の速さ)
 前記方法で作製した評価用トレスをプレーンシャンプーで洗浄後、軽く水気を取り、表1に記載のコンディショナー1gを塗布した後、水道水ですすぎ、60秒間自然排水した後、トレスの上に、ペーパータオル(大王製紙社製、エリエールプロワイプ)、アクリル板、錘(アクリル板と錘の総重量1.3kg)を順に乗せ、余分な水分を除去した。
 この毛髪トレスを下向きに設置し、ドライヤー(Tescom社製、Nobby NB2501)の吹き出し口から毛髪トレスの毛髪中心部までの距離が45cmになるようにドライヤー(弱温風モード:600W)を固定した。次いで、4秒に1回ずつ指を通しながらドライヤー乾燥を行った。この際、ドライヤー乾燥開始から、毛髪が完全に乾いたと研究員が判断できるまでの時間(秒)を計測した。この操作及び計測を3回繰り返し、その平均値を速乾性評価とした。
(Speed of drying)
After washing the evaluation tress made by the above method with a plain shampoo, lightly drain it, apply 1g of the conditioner shown in Table 1, rinse with tap water, let it drain naturally for 60 seconds, and then place a paper towel on the tress. (Daiou Paper Co., Ltd., Erière Pro Wipe), acrylic plate, weight (total weight of acrylic plate and weight 1.3 kg) were placed in order to remove excess water.
This hair tress was placed face down, and the dryer (low warm air mode: 600 W) was fixed so that the distance from the outlet of the dryer (manufactured by Tescom, Nobby NB2501) to the hair center of the hair tress was 45 cm. Next, the dryer was dried while passing a finger once every 4 seconds. At this time, the time (seconds) from the start of drying the dryer until the researcher was able to determine that the hair was completely dried was measured. This operation and measurement were repeated three times, and the average value was used for quick drying evaluation.
Figure JPOXMLDOC01-appb-T000011
Figure JPOXMLDOC01-appb-T000011
*1:ファーミンDM-E80(花王社製)
*2:NIKKOLアミドアミンMPS(日本サーファクタント工業社製)
*3:アミデットAPA-22(花王スペイン社製)
*4:コータミン2285E-(E)(花王社製)
*5:コータミン60W(花王社製)
*6:カルコール8098(花王社製)
*7:カルコール6098(花王社製)
*8:ABIL SOFT AF100(エヴォニック インダストリー社製;粘度400mm2/s)
*9:Silsense A21(ルブリゾール社製;粘度250mm2/s)
*10:XS65-C0032(モメンティブ・パフォーマンス・マテリアルズ・ジャパン合同会社)
*11:TMF-1.5(信越化学工業社製;沸点191℃)
*12:シリコーンSH245FLUID(東レ・ダウコーニング社製;沸点205℃)
* 1: Farmin DM-E80 (manufactured by Kao Corporation)
* 2: NIKKOL Amidoamine MPS (manufactured by Nippon Surfactant Kogyo Co., Ltd.)
* 3: Amidet APA-22 (Kao Spain)
* 4: Cotamine 2285E- (E) (Kao Corporation)
* 5: Cotamin 60W (Kao Corporation)
* 6: Calcoal 8098 (Kao Corporation)
* 7: Calcoal 6098 (Kao Corporation)
* 8: ABIL SOFT AF100 (Evonik Industry Co., Ltd .; viscosity 400mm 2 / s)
* 9: Silsense A21 (manufactured by Lubrizol; viscosity 250mm 2 / s)
* 10: XS65-C0032 (Momentive Performance Materials Japan GK)
* 11: TMF-1.5 (manufactured by Shin-Etsu Chemical Co., Ltd .; boiling point 191 ° C)
* 12: Silicone SH245FLUID (manufactured by Dow Corning Toray; boiling point 205 ° C)

Claims (7)

  1.  成分(A)~(D)及び水を含有する、毛髪に適用した後洗い流して使用される毛髪化粧料。
     (A) カチオン界面活性剤
     (B) 高級アルコール
     (C) ポリオキシアルキレン側鎖及びアミノアルキル側鎖を有するシリコーン
     (D) 揮発性シリコーン
    A hair cosmetic comprising components (A) to (D) and water, which is used after being applied to hair and washed away.
    (A) Cationic surfactant (B) Higher alcohol (C) Silicone having polyoxyalkylene side chain and aminoalkyl side chain (D) Volatile silicone
  2.  成分(D)に対する成分(C)の質量比(C)/(D)が0.01以上5以下である請求項1に記載の毛髪化粧料。 The hair cosmetic according to claim 1, wherein the mass ratio (C) / (D) of the component (C) to the component (D) is 0.01 or more and 5 or less.
  3.  成分(C)の25℃における粘度が4000mm2/s以下である請求項1又は2に記載の毛髪化粧料。 The hair cosmetic composition according to claim 1 or 2, wherein the viscosity of component (C) at 25 ° C is 4000 mm 2 / s or less.
  4.  成分(D)が、1013.25hPa下における沸点が260℃以下の鎖状及び環状のシリコーン油からなる群より選択される1種又は2種以上である請求項1~3のいずれか1項に記載の毛髪化粧料。 The component (D) is one or more selected from the group consisting of linear and cyclic silicone oils having a boiling point of 260 ° C or lower under 1013.25 hPa. Hair cosmetics.
  5.  成分(C)が、下記一般式(7)で表されるものである請求項1~4のいずれか1項に記載の毛髪化粧料。
    Figure JPOXMLDOC01-appb-C000001
    〔式中、rは1~50の整数、sは1~50の整数、tは1~50の整数、aは0~50の整数、bは0~50を示し(aとbとが同時に0になることはない)、カッコ内の各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。R9は炭素数1~6の2価の炭化水素基を示し、R10は-R11Zで表されるアミノ基又はアンモニウム基を有する置換基を示す。ここで、R11は炭素数1~6の2価の炭化水素基を示し、Zは-NR12 2、-NR12(CH2)cNR12 2、及び-NR12(CH2)cNR12C=O(R13)からなる群より選ばれる1価の基を示し、R12は水素原子又は炭素数1~4の炭化水素基を示し、R13は炭素数1~4の炭化水素基を示し、cは2~6の整数を示し、R14は炭素数1~4の炭化水素基又はトリメチルシリル基を示す。〕
    The hair cosmetic composition according to any one of claims 1 to 4, wherein the component (C) is represented by the following general formula (7).
    Figure JPOXMLDOC01-appb-C000001
    [Wherein, r is an integer of 1 to 50, s is an integer of 1 to 50, t is an integer of 1 to 50, a is an integer of 0 to 50, b is 0 to 50 (a and b are simultaneously (It is never 0), and the bonding order of the structural units in the parenthesis is not limited, and the bonding form may be block or random. R 9 represents a divalent hydrocarbon group having 1 to 6 carbon atoms, and R 10 represents a substituent having an amino group or an ammonium group represented by —R 11 Z. Here, R 11 represents a divalent hydrocarbon group having 1 to 6 carbon atoms, and Z represents —NR 12 2 , —NR 12 (CH 2 ) c NR 12 2 , and —NR 12 (CH 2 ) c NR 12 represents a monovalent group selected from the group consisting of C═O (R 13 ), R 12 represents a hydrogen atom or a hydrocarbon group having 1 to 4 carbon atoms, and R 13 represents a hydrocarbon having 1 to 4 carbon atoms. C represents an integer of 2 to 6, and R 14 represents a hydrocarbon group having 1 to 4 carbon atoms or a trimethylsilyl group. ]
  6.  成分(D)が、式(8)で表される鎖状シリコーン、一般式(9)で表される鎖状シリコーン、及び一般式(10)で表される環状シリコーンからなる群より選ばれる1種又は2種以上の揮発性シリコーンである請求項1~5のいずれか1項に記載の毛髪化粧料。
    Figure JPOXMLDOC01-appb-C000002
    The component (D) is selected from the group consisting of a chain silicone represented by the formula (8), a chain silicone represented by the general formula (9), and a cyclic silicone represented by the general formula (10) The hair cosmetic composition according to any one of claims 1 to 5, which is a seed or two or more volatile silicones.
    Figure JPOXMLDOC01-appb-C000002
  7.  請求項1~6のいずれか1項に記載の毛髪化粧料を毛髪に塗布し、水で洗い流す毛髪処理方法。 A hair treatment method in which the hair cosmetic composition according to any one of claims 1 to 6 is applied to hair and rinsed with water.
PCT/JP2016/085039 2015-12-02 2016-11-25 Hair cosmetic WO2017094625A1 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
SG11201804615SA SG11201804615SA (en) 2015-12-02 2016-11-25 Hair cosmetic

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP2015235684 2015-12-02
JP2015-235684 2015-12-02

Publications (1)

Publication Number Publication Date
WO2017094625A1 true WO2017094625A1 (en) 2017-06-08

Family

ID=58796647

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/JP2016/085039 WO2017094625A1 (en) 2015-12-02 2016-11-25 Hair cosmetic

Country Status (4)

Country Link
JP (1) JP6186065B2 (en)
SG (1) SG11201804615SA (en)
TW (1) TWI735485B (en)
WO (1) WO2017094625A1 (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2019031143A1 (en) * 2017-08-10 2019-02-14 花王株式会社 Hair cosmetic
WO2020008812A1 (en) * 2018-07-02 2020-01-09 花王株式会社 Hair cosmetic

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2024070386A1 (en) * 2022-09-29 2024-04-04 花王株式会社 Hair treatment agent or head decoration product fiber treatment agent

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2006265205A (en) * 2005-03-25 2006-10-05 Kose Corp Hair conditioning composition
JP2014073970A (en) * 2012-10-02 2014-04-24 Asahi Kasei Chemicals Corp Hair treatment agent

Family Cites Families (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2906201B2 (en) * 1992-12-09 1999-06-14 花王株式会社 Hair cosmetics
EP1817001A1 (en) * 2004-11-24 2007-08-15 Wella Aktiengesellschaft Hair treatment agent
JP4719575B2 (en) * 2006-01-13 2011-07-06 花王株式会社 Hair cosmetic and method for producing the same
JP5189807B2 (en) * 2006-08-23 2013-04-24 花王株式会社 Aqueous hair cosmetics
JP5758071B2 (en) * 2009-11-03 2015-08-05 株式会社ミルボン Hairdressing fee
US20120276035A1 (en) * 2011-04-29 2012-11-01 Kenra Professional, Llc Composition for Reducing the Time Needed to Dry Wet Hair
US10716747B2 (en) * 2012-11-01 2020-07-21 Henkel IP & Holding GmbH Serum for reducing the time needed to dry wet hair

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2006265205A (en) * 2005-03-25 2006-10-05 Kose Corp Hair conditioning composition
JP2014073970A (en) * 2012-10-02 2014-04-24 Asahi Kasei Chemicals Corp Hair treatment agent

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2019031143A1 (en) * 2017-08-10 2019-02-14 花王株式会社 Hair cosmetic
JP2019034928A (en) * 2017-08-10 2019-03-07 花王株式会社 Hair cosmetic
WO2020008812A1 (en) * 2018-07-02 2020-01-09 花王株式会社 Hair cosmetic
JP2020007296A (en) * 2018-07-02 2020-01-16 花王株式会社 Hair cosmetic
JP7358080B2 (en) 2018-07-02 2023-10-10 花王株式会社 hair cosmetics

Also Published As

Publication number Publication date
JP6186065B2 (en) 2017-08-23
SG11201804615SA (en) 2018-06-28
TWI735485B (en) 2021-08-11
JP2017105760A (en) 2017-06-15
TW201728322A (en) 2017-08-16

Similar Documents

Publication Publication Date Title
KR101196280B1 (en) Hair cosmetics
TWI736624B (en) Hair treatment agent
JP4185467B2 (en) Hair cosmetics
JP4210614B2 (en) Hair cosmetics
WO2004047777A1 (en) Cosmetic hair preparation
JP2017210413A (en) Hair treatment agent
JP6186065B2 (en) Hair cosmetics
JP4422508B2 (en) Hair cosmetics
TWI673064B (en) Hair cosmetic
JP4926371B2 (en) Hair cosmetics
JP2017019748A (en) Hair cosmetic
JP6301642B2 (en) Hair cosmetics
JP6896381B2 (en) Hair cosmetics
JP2016121091A (en) Hair cosmetic
JP2005272377A (en) Hair cosmetic
JP6490449B2 (en) Hair cosmetics
JP6718705B2 (en) Hair cosmetics
TWI827617B (en) hair cosmetics
JP6718706B2 (en) Hair cosmetics
TW201601771A (en) Hair cosmetic composition
JP6345034B2 (en) Hair treatment method
JP2005272390A (en) Hair cosmetic
JP2005272379A (en) Hair cosmetic
JP2005272391A (en) Hair cosmetic

Legal Events

Date Code Title Description
121 Ep: the epo has been informed by wipo that ep was designated in this application

Ref document number: 16870562

Country of ref document: EP

Kind code of ref document: A1

WWE Wipo information: entry into national phase

Ref document number: 11201804615S

Country of ref document: SG

NENP Non-entry into the national phase

Ref country code: DE

122 Ep: pct application non-entry in european phase

Ref document number: 16870562

Country of ref document: EP

Kind code of ref document: A1