Fiber treatment agent composition

A fiber treatment composition with a self-crosslinking compound and additional components forms a durable coating on hair, addressing the issue of dull color and friction by enhancing color darkness and reducing surface friction.

JP2025131791APending Publication Date: 2025-09-09KAO CORP
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Patent Information

Application Number
JP2025096923
Authority / Receiving Office
JP · JP
Patent Type
Applications
Current Assignee / Owner
Priority Date
2019-12-23
Filing Date
2025-06-10
Publication Date
2025-09-09

AI Technical Summary

Technical Problem

Existing hair treatment methods, such as those described in Patent Document 1, do not sufficiently improve color saturation and maintain the appearance of damaged hair, leading to issues like dullness and increased friction.

Method used

A fiber treatment composition comprising a self-crosslinking compound, non-volatile silicone, polyhydric alcohol polymer, fatty acid ester, and acrylic resin, along with a color deepening agent, is applied to the hair surface and dried without rinsing, forming a thick coating that enhances color darkness and reduces friction.

Benefits of technology

The composition effectively darkens the hair color and reduces friction, maintaining the effect even after multiple washes by forming a durable, thick coating on the hair surface.

✦ Generated by Eureka AI based on patent content.

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Abstract

To provide a fiber treatment agent composition which can make the color of a fiber surface such as hair appear deeper, and can maintain this effect even when hair is repeatedly washed after treatment.SOLUTION: A fiber treatment agent composition comprising the following components (A) and (B), wherein a content of the component (A) is 0.05 mass% or more and 5.0 mass% or less, a content of the component (B) is 0.05 mass% or more and 10.0 mass% or less, and a mass ratio (B) / (A) of the component (B) to the component (A) is 3 or more and 10 or less. (A): one or more self-crosslinking compounds selected from the group consisting of an epoxyaminosilane copolymer and an alkoxysilyl group-containing alkylamine. (B): a color deepening agent comprising polyquaternium-37.SELECTED DRAWING: None
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Description

[Technical Field]

[0001] The present invention relates to a fiber treatment composition. [Background technology]

[0002] In recent years, in addition to chemical treatments such as hair coloring and perms, it has become a habit, especially among young women. Hair styling using heat from hair irons, hair dryers, etc. can cause hair to dry out, especially at the ends. Damage to hair is becoming more serious. Hair damage causes the hair surface to become hydrophilic and friction to increase. As a result, problems such as tangled ends and difficulty running your fingers through your hair when styling occur. As a result of the formation of cavities inside the hair, light is diffused, making the hair appear whitish and unhealthy. This causes the problem that

[0003] As a technology for improving the color of damaged hair, Patent Document 1 discloses a method for improving the color of damaged hair by using an amino group or a quaternary Washing and conditioning hair with shampoo containing water-insoluble modified silicone containing ammonium groups Treatment with conditioner will brighten up the original color of hair that has become dull due to damage. It is disclosed that the color appears brighter and the color saturation is increased. [Prior art documents] [Patent documents]

[0004] [Patent Document 1] Japanese Patent Application Laid-Open No. 2006-206585 Summary of the Invention [Problem to be solved by the invention]

[0005] However, the technology described in Patent Document 1 does not improve color saturation sufficiently, and the color saturation of damaged hair is not improved sufficiently. This technology was not satisfactory as an appearance improvement technique.

[0006] Therefore, the present invention is capable of treating fibers such as hair to make the color of the fiber surface appear darker. Moreover, this effect can be maintained even if the hair is washed repeatedly after treatment. The present invention relates to a fiber treatment composition. [Means for solving the problem]

[0007] As a result of intensive research, the present inventors have found that a specific self-crosslinking compound can be formed on the surface of a fiber. The above problem can be solved by using a component that can increase the thickness of the coating to be applied. This finding led to the completion of the present invention.

[0008] The present invention comprises the following components (A) and (B), and the content of component (A) is 0.05 mass% or more and 5.0 mass% or less. % or less, the content of component (B) is 0.05% by mass or more and 10.0% by mass or less, and the ratio of component (B) to component (A) The present invention provides a fiber treatment composition having a mass ratio (B) / (A) of 150 or less. (A) Self-crosslinking compound (B) Non-volatile silicone, polyhydric alcohol polymer, fatty acid ester and acrylic resin one or more color deepening agents selected from the group consisting of (excluding those corresponding to component (A))

[0009] The present invention also provides a method for treating a fiber by applying the fiber treatment composition to the surface of a fiber and then drying the composition without rinsing it off. A method for treating fibers is provided.

[0010] Furthermore, the present invention provides a method for producing a fiber by applying a composition containing the following component (A) to a fiber surface and then drying the composition: Instead, a composition containing the following component (B) is applied to the area to be treated, and the composition is allowed to dry without rinsing. A method for treating fibers is provided. (A) Self-crosslinking compound (B) Non-volatile silicone, polyhydric alcohol polymer, fatty acid ester and acrylic resin one or more color deepening agents selected from the group consisting of (excluding those corresponding to component (A))

[0011] Furthermore, the present invention provides a method for producing a fiber by applying a composition containing the following component (B) to a fiber surface and then drying the composition: Instead, a composition containing the following component (A) is applied to the area to be treated, and the composition is allowed to dry without rinsing. A method for treating fibers is provided. (A) Self-crosslinking compound (B) Non-volatile silicone, polyhydric alcohol polymer, fatty acid ester and acrylic resin one or more color deepening agents selected from the group consisting of (excluding those corresponding to component (A)) [Effects of the Invention]

[0012] The fiber treatment composition of the present invention can make the color of the surface of fibers such as hair appear darker. DETAILED DESCRIPTION OF THE INVENTION

[0013] [Component (A): Self-crosslinking compound] Examples of the self-crosslinking compound of component (A) include the following components (A1) to (A3). (A1) Alkoxysilyl group-containing silicone (A2) Alkoxysilyl group-containing acrylate compound (A3) Alkoxysilyl group-containing alkylamine

[0014] Components (A1) to (A3) are all alkoxysilyl groups -SiR 1 n (OR 2 ) 3-n [In the formula, R 1 and R 2 each independently represents a monovalent hydrocarbon group, and n represents a number from 0 to 2. It has.

[0015] The alkoxysilyl group-containing silicone of component (A1) is a silicone in which the alkoxysilyl group is an organosilyl group. It is bonded to a polysiloxane residue.

[0016] In this case, the organopolysiloxane residue contains an amino group, and more preferably contains an amino group and Component (A1) specifically includes the following epoxyaminosilanes: copolymer, (amodimethicone / morpholinomethylsilsesquioxane) copolymer. Of these, epoxy amino silane copolymers are preferred.

[0017] The epoxy amino silane copolymer is a reaction product of the following compounds (a) to (d): (a) Polysiloxanes containing at least two oxiranyl or oxetanyl groups (b) Polyethers containing at least two oxiranyl or oxetanyl groups (c) Aminopropyltrialkoxysilane (d) Compounds selected from the group consisting of the following primary and secondary amines: Primary amines: methylamine, ethylamine, propyleneamine, ethanolamine, Isopropylamine, butylamine, isobutylamine, hexylamine, dodecylamine amine, oleylamine, aniline, aminopropyltrimethylsilane, aminopropyltrimethylsilane Ethylsilane, aminomorpholine, aminopropyldiethylamine, benzylamine, Butylamine, 3-amino-9-ethylcarbazole, 1-aminoheptafluorohexane, 2,2,3 ,3,4,4,5,5,6,6,7,7,8,8,8-Pentadecafluoro-1-octanamine Secondary amines: methylethylamine, methyloctadecylamine, diethanolamine , dibenzylamine, dihexylamine, dicyclohexylamine, piperidine, pyrrolidin Phthalimide, polymer amine

[0018] <Compounds (a), (b)> The compound (a) is a polysiloxane containing at least two oxiranyl or oxetanyl groups. Examples of suitable oxanes include those represented by the following general formula (1):

[0019] [ka]

[0020] [wherein R has an oxiranyl group or an oxetanyl group at the terminal, and may contain a heteroatom] represents a hydrocarbon group having 1 to 6 carbon atoms, and x represents a number from 1 to 1000.

[0021] Compound (b) is a polyethylene containing at least two oxiranyl or oxetanyl groups. Examples of such ethers include those represented by the following general formula (2):

[0022] [ka]

[0023] [wherein R has the same meaning as above, y is 1 to 100, z is 0 to 100, and y+z is 1 to 20] Indicates a number that is 0.]

[0024] In the general formulas (1) and (2), the heteroatom that R may contain is preferably an oxygen atom. R can be an oxiranylmethyl group (glycidyl group), an oxiranylmethoxy group (glycidyl group), or glycidyloxy group), oxiranylmethoxypropyl group (glycidyloxypropyl group), Oxetanylmethyl group, oxetanylmethoxy group, oxetanylmethoxypropyl group, 3-ethoxy Among them, heteroacids having an oxiranyl group are preferred. A hydrocarbon group having 1 to 4 carbon atoms which may contain a nitrogen atom is preferred, and an oxiranylmethyl group (a group Glycidyloxy group), oxiranylmethoxy group (glycidyloxy group), oxiranylmethoxy Propyl groups (glycidyloxypropyl groups) are more preferred. .

[0025] <Compound (c)> Compound (c) is an aminopropyltrialkoxysilane. The oxy group may have 1 to 6 carbon atoms, and may further have 2 to 4 carbon atoms, or may further have 3 carbon atoms. The compound (c) is preferably an amino group, and is particularly preferably an isopropoxy group. Propyltrimethoxysilane, aminopropyltriethoxysilane, aminopropyltri Propoxysilane, aminopropyltriisopropoxysilane, aminopropyltributyrate tert-butoxysilane, aminopropyltri-tert-butoxysilane, among which aminopropyltri-tert-butoxysilane The compound (c) may be any one of them alone or in combination of two or more. The above can be used in combination.

[0026] <Compound (d)> Compound (d) is a compound selected from the group consisting of the following primary and secondary amines: . Primary amines: methylamine, ethylamine, propyleneamine, ethanolamine, Isopropylamine, butylamine, isobutylamine, hexylamine, dodecylamine amine, oleylamine, aniline, aminopropyltrimethylsilane, aminopropyltrimethylsilane Ethylsilane, aminomorpholine, aminoethyldimethylamine, aminoethyldiethyl Amines, aminoethyl dibutylamine, aminopropyl dimethylamine, aminopropyl Diethylamine, aminopropyldibutylamine, benzylamine, naphthylamine, 3- Amino-9-ethylcarbazole, 1-aminoheptafluorohexane, 2,2,3,3,4,4,5,5,6,6,7 ,7,8,8,8-Pentadecafluoro-1-octanamine Secondary amines: methylethylamine, methyloctadecylamine, diethanolamine , dibenzylamine, dihexylamine, dicyclohexylamine, piperidine, pyrolyl Diphthalimide, polymer amine

[0027] Of these, primary amines are preferred, and aminopropyldiethylamine, aminopropyldiethylamine, At least one selected from the group consisting of propyl dimethylamine and aminopropyl dibutylamine The compound (d) may be used alone or in combination of two or more. can.

[0028] The reaction of compounds (a) to (d) can be carried out, for example, by refluxing in a solvent such as isopropanol for a certain period of time. Here, the oxiranyl or oxetanyl groups of the compounds (a) and (b) The molar ratio of compound (c) to amino groups is preferably 1 or more, more preferably 1.1 or more, and even more preferably 1.2 or more. It is preferably 1.2 or more, and is preferably 4 or less, more preferably 3.9 or less, and even more preferably Preferably, it is 3.8 or less.

[0029] Among the components (A1), the epoxy aminosilane copolymer is INCI Polysilicone-29. Silsoft CLX-E (manufactured by Momentive Performance Materials; active ingredient: 1 5% by mass, including dipropylene glycol and water). As for the (amodimethicone / morpholinomethylsilsesquioxane) copolymer, Bels Examples include il ADM 6300 and 8301 (manufactured by Asahi Kasei Wacker Co., Ltd.).

[0030] The alkoxysilyl group-containing acrylate compound of component (A2) is an alkoxysilyl group-containing acrylate compound It is a compound bonded to a group represented by the following general formula (3).

[0031] [ka]

[0032] [In the formula, R 3 represents a hydrogen atom or a methyl group, and R 4 is a divalent saturated hydrocarbon group having 1 to 6 carbon atoms indicates.]

[0033] R in general formula (3) 4 As the alkyl group, those having 2 to 4 carbon atoms are preferred, and among them, trimethyl The component (A2) is preferably a 3-methacryloxypropylmethyldimethoxysilane. (KBM-502; Shin-Etsu Chemical Co., Ltd.), 3-methacryloxypropyltrimethoxysilane (KBM -503; Shin-Etsu Chemical Co., Ltd.), 3-methacryloxypropylmethyldiethoxysilane (KBE-50 2; Shin-Etsu Chemical Co., Ltd.), 3-methacryloxypropyltriethoxysilane (KBE-503; Shin-Etsu Chemical Co., Ltd.), Chemical Industry Co., Ltd.), 3-acryloxypropyltrimethoxysilane (KBM-5103; Shin-Etsu Chemical Co., Ltd.), Examples of suitable silane coupling agents include those manufactured by Epson Corporation.

[0034] The alkoxysilyl group-containing alkylamine of component (A3) is an alkylamine in which the alkoxysilyl group is It is a compound bonded to a group represented by general formula (4).

[0035] [ka]

[0036] [In the formula, R 5 and R 6 represents a hydrocarbon group which may be substituted with a hydrogen atom or an amino group. or they may together form an alkylidene group, R 7 is a divalent carbon atom with 1 to 6 carbon atoms represents a hydrocarbon group.

[0037] R in general formula (4) 7 As the alkyl group, those having 2 to 4 carbon atoms are preferred, and among them, trimethyl The component (A3) is preferably an N-2-(aminoethyl)-3-aminopropylmethyldiphenylamine. Methoxysilane (KBM-602; Shin-Etsu Chemical Co., Ltd.), N-2-(aminoethyl)-3-aminopropyl Trimethoxysilane (KBM-603; Shin-Etsu Chemical Co., Ltd.), 3-aminopropyltrimethoxysilane Lan (KBM-903; Shin-Etsu Chemical Co., Ltd.), 3-aminopropyltriethoxysilane (KBE-903; Shin-Etsu Chemical Co., Ltd.), 3-triethoxysilyl-N-(1,3-dimethyl-butylidene)propylamine (KBE-9103P; Shin-Etsu Chemical Co., Ltd.), N-phenyl-3-aminopropyltrimethoxysilane (KBM-573; Shin-Etsu Chemical Co., Ltd.), N-(vinylbenzyl)-2-aminoethyl-3-aminopropyl and the hydrochloride salt of methyltrimethoxysilane (KBM-575; manufactured by Shin-Etsu Chemical Co., Ltd.). -Aminopropyl-triethoxysilane, 3-aminopropylmethyldiethoxysilane, N-(2 -aminoethyl)-3-aminopropyltriethoxysilane, 3-(2-aminoethylamino)propanol Pyrmethyldiethoxysilane and the like are preferred.

[0038] The content of component (A) in the fiber treatment composition of the present invention is such that it has excellent film-forming properties and From the viewpoint of the development of the accompanying darkening effect on the fiber surface, the content is 0.05 mass % or more, preferably 0.1 % by mass or more, more preferably 0.2% by mass or more, and even more preferably 0.25% by mass or more. Furthermore, it is 5.0% by mass or less, preferably 3.0% by mass or less, and more preferably 1.0% by mass or less. , and more preferably 0.5 mass % or less.

[0039] [Component (B): Color deepening agent] Component (B) is a non-volatile silicone, a polyhydric alcohol polymer, a fatty acid ester, and an acrylic acid. The component (A) is one or more color deepening agents selected from the group consisting of acrylic resins. The self-crosslinking compound is excluded from component (B). By increasing the thickness of the coating formed on the fiber surface, the color of the fiber surface appears darker. It is a component that can

[0040] Non-volatile silicones include dimethylpolysiloxane, amino-modified polysiloxane, Phenyl-modified polysiloxane, polyglycerin-modified polysiloxane, silicone resin, Acrylic-modified polysiloxane, alkyl-modified polysiloxane, methacrylic-modified polysiloxane carboxyl-modified polysiloxane, aminopolyether-modified polysiloxane, oxalyl-modified polysiloxane Sazoline-modified polysiloxane, polyether-modified polysiloxane, fluorine-modified polysiloxane San, mercapto-modified polysiloxane, hydrogen-modified polysiloxane, aralkyl Modified polysiloxane, epoxy modified polysiloxane, hydroxy modified polysiloxane, etc. Among them, oxazoline-modified polysiloxane is preferred, and polysilicone-9 is preferred. is more preferred.

[0041] Examples of polyhydric alcohol polymers include diethylene glycol, dipropylene glycol, Polyethylene glycol, polypropylene glycol, tetraethylene glycol, diglyceride Phosphorus, polyethylene glycol, triglycerin, tetraglycerin, polyglycerin, etc. Examples include:

[0042] Fatty acid esters include lauric acid esters, myristic acid esters, and palmitic acid esters. Esters, oleates, phthalates, adipates, caprylates ester, capric acid ester, behenic acid ester, methacrylic acid ester, ethylhexyl The alcohol component in these fatty acid esters is , methanol, ethanol, propanol, butanol, pentanol, hexanol, Heptanol, octanol, decanol, 2-ethylhexanol, lauryl alcohol Myristyl alcohol, cetyl alcohol, stearyl alcohol, isostearyl Alcohol, Oleyl Alcohol, Behenyl Alcohol, Isopropyl Alcohol, Isopropyl Monohydric alcohols such as isobutyl alcohol and isodecyl alcohol; ethylene glycol, Propylene glycol, butylene glycol, diethylene glycol, triethylene glycol Dihydric alcohols such as ethanol; glycerin, trimethylolpropane, triethanolamine Trihydric alcohols such as pentaerythritol, diglycerin, xylose, sorbitan tetrahydric alcohols such as xylitol, triglyceride, glucose, fructose, etc.; pentahydric alcohols such as xylitol, triglyceride, glucose, fructose, etc. Hexahydric alcohols such as sorbitol, malbitol, tetraglycerin, etc.; more than 6 Polyglycerol with hydroxyl groups; disaccharides such as sucrose, trehalose, and lactose; maltodextrin Examples include trisaccharides such as triose.

[0043] Examples of the acrylic resin include polymers containing a repeating unit represented by the following general formula (5): can be.

[0044] [ka]

[0045] [In the formula, R 8 represents a hydrogen atom, a methyl group, or an ethyl group, and X 1 represents an oxygen atom or an imino group. And X 1 When is an oxygen atom, -Y 1 -X 2 is a hydrogen atom, and is an alkyl group with 1 to 24 carbon atoms. alkyl group, isobornyl group, -(CH2) p -N(R 9 )2, -(CH2) p -N + (R 9 )3, -(CH2) p -OR 9 , -C(CH3)2-N(R 9 )2 or -C(CH3)2-OR 9 (p is a number between 1 and 3. and R 9 represents a hydrogen atom or an alkyl group having 1 to 4 carbon atoms), or Y 1 represents a group consisting of an oxyethylene group and / or an oxypropylene group, and X 2 Water represents a hydrogen atom, a methyl group, or an ethyl group, and X 1If is NH, then Y 1 is a compound with 1 to 3 carbon atoms represents the following divalent saturated hydrocarbon group, and X 2 -N(R 9 )2(R 9 indicates the same as above) . ]

[0046] Such acrylic resins include poly(methacryloyloxyethyltrimethylanthracene) and poly(methacryloyloxyethyltrimethylanthracene). ammonium chloride) (INCI name: Polyquaternium-37, e.g., BASF Cosmedium Lutragel 300), vinylpyrrolidone-N,N-dimethylaminoethyl methacrylate copolymer Polyquaternium-11 (INCI name: Polyquaternium-11, e.g., Gafcut 734, manufactured by ISP) Fukat 755N, Gaffcut 755N-O), Acrylates / C 1-18 Alkyl acrylates / C 1- 8 Alkyl acrylamide copolymer (e.g., Goo Chemical Industry Co., Ltd., Plussize L-9909B) ; 2-amino-2-methyl-1-propyl alcohol neutralization product of the polymer).

[0047] Among these components (B), polysilicone-9, polyquaternium-37, polyethylene glycol Recall is preferred.

[0048] The content of component (B) in the fiber treatment composition of the present invention is such that an excellent color deepening effect is exhibited. From the viewpoint of the present invention, the content of the hydroxybenzoates is 0.05% by mass or more, preferably 0.5% by mass or more, and more preferably 1.0% by mass or more. % by mass or more, and more preferably 1.5% by mass or more. In addition, excellent film forming properties and the resulting fiber From the viewpoint of achieving a darkening effect on the fiber surface, the content is 10.0 mass % or less, and preferably 7.0 mass % It is preferably 5.0% by mass or less, more preferably 2.5% by mass or less.

[0049] The mass ratio (B) / (A) of the component (B) to the component (A) in the fiber treatment composition of the present invention is preferably From the viewpoint of excellent film forming properties and the accompanying darkening effect, it is preferably 150 or less. is 100 or less, more preferably 10 or less, and from the viewpoint of exhibiting an excellent color deepening effect, It is preferably 0.05 or more, and more preferably 3 or more.

[0050] [Component (C): Micelle formation inhibitor] Among the components (A), the aforementioned epoxy amino silane copolymers such as Polysilicone-29 are hydrophobic. As a result of the polysiloxane moiety and the hydrophilic polyether moiety, the micelle formation ability is improved. Therefore, the compound has the characteristic of forming molecular aggregates (micelles) in water. When used in combination with an agent (component (C)) that inhibits the micelle formation ability, it is possible to impart hydrophobicity to the fibers and This can further improve the friction-reducing effect and the durability of these effects.

[0051] Examples of the micelle formation inhibitor of component (C) include the following (C1) to (C3). (C1): The hydrogen bond term of the Hansen solubility parameter is 10.0 MPa 1 / 2 Over 15.8MPa 1 / 2 Below Certain organic compounds (excluding those falling under (C3)) (C2): Ethanol, triethylene glycol, pentylene glycol, methylpropional a compound selected from diethanolamine, diethanolamine, and N-methyldiethanolamine (C3): Organic salt

[0052] In the present invention, the hydrogen bond term of the Hansen Solubility Parameter is Software based on "Parameters: A User's Handbook," CRC Press, Boca Raton FL, 2007 The calculation was performed at 25°C in the DIY program using the HSPiP 4th Edition 4.1.07 package. δ H (MPa 1 / 2 ) (energy term due to intermolecular hydrogen bonds).

[0053] The hydrogen bond term of the Hansen solubility parameter of component (C1) is 10.0 MPa. 1 / 2 Over 15.8M Pa 1 / 2 The organic compounds having the following carbon atoms are straight-chain or branched-chain alkyl Aliphatic alcohols, aromatic alcohols, and ether alcohols with a group and one or more hydroxyl groups N-alkylpyrrolidone, acyclic ester, alkylamine which may have a hydroxyl group, etc. Examples include organic compounds.

[0054] Below, the hydrogen bond term of Hansen's solubility parameter is 10.0 MPa. 1 / 2 Over 15.8MPa 1 / 2 Below The following are specific examples of compounds. The values ​​in parentheses in each example are the water content calculated using the method described above. It is a prime bond term. -Aliphatic alkyl groups having 2 to 8 carbon atoms, either linear or branched, and one or more hydroxyl groups Examples of alcohols: 1-propanol (14.7), 2-propanol (14.3), 1-butanol (1 Lower alkanols such as 2-butanol (12.4), hexylene glycol (15.0), Polyhydric alcohols such as octanediol (14.5) and decanediol (12.8) Examples of aromatic alcohols: benzyl alcohol (12.4), cinnamyl alcohol (10.9) ), phenethyl alcohol (11.4), p-anisyl alcohol (12.1), p-methylbenzyl Alcohol (11.2), phenoxyethanol (12.2), 2-benzyloxyethanol (10 .8), 2-phenyl-1-propanol (10.2) Examples of ether alcohols: ethylene glycol monoethyl ether (15.7), ethylene glycol monoethyl ether (15.8), Diethylene glycol monobutyl ether (13.0), diethylene glycol monomethyl ether ( 13.1), Diethylene glycol monoethyl ether (11.9), Diethylene glycol mono Butyl Ether (11.7), Ethylhexyl Glyceryl Ether (13.1) Example of N-alkylpyrrolidone: N-(2-hydroxyethyl)-2-pyrrolidone (13.5) Examples of acyclic esters: ethyl lactate (14.4), butyl lactate (11.9) Examples of alkylamines that may have a hydroxyl group: methylamine (13.0), ethylamine ( 10.2), N,N-dimethylmonoethanolamine (13.1), aminomethylpropanol (14.4) )

[0055] Among these, from the viewpoint of expressing the micelle formation inhibition ability, Hansen solubility parameter The hydrogen bond term is 15.5 MPa 1 / 2 Preferably, it is 15.0 MPa or less. 1 / 2 Less than or equal to Preferably, 13.0 MPa 1 / 2 More preferably, it is 12.5 MPa or less. 1 / 2 which is further From the same viewpoint, 10.5 MPa is more preferable. 1 / 2 Preferably, it is 11.0 MPa or more. 1 / 2 End More preferably, it is 11.5 MPa. 1 / 2 More preferably, it is 12.0 MPa or more. 1 / 2End Among these, aromatic alcohols and ether alcohols are preferred. Preferably, benzyl alcohol (12.4), phenethyl alcohol (11.4), phenoxyethanol at least one selected from 2-benzyloxyethanol (12.2) and 2-benzyloxyethanol (10.8); More preferable.

[0056] Among the components (C), (C2) ethanol, triethylene glycol, pentylene glycol, Selected from methylpropanediol, diethanolamine, and N-methyldiethanolamine The compound has a hydrogen bond term in the Hansen solubility parameter of 15.8 MPa. 1 / 2 More than These compounds have the ability to inhibit micelle formation.

[0057] Among the components (C), the organic salts of (C3) include guanidine salts having a guanidinium group, arginine salts, and the like. At least one selected from guanidine salts is preferred. Guanidine hydrochloride, guanidine nitrate, guanidine phosphate, guanidine thiocyanate, guanidine Guanidine carbonate, guanidine acetate, guanidine sulfate, guanidine sulfamate, amine At least one selected from the group consisting of aminoguanidine hydrochloride and aminoguanidine sulfate is included. For example, arginine salts include arginine hydrochloride, arginine nitrate, and arginine phosphate. salt, arginine thiocyanate, arginine carbonate, arginine acetate, arginine sulfate Arginine Glutamate, Arginine Sulfamate, Arginine Glutamate, and Arginine Aspartate At least one selected from the group consisting of hydroxybenzoates and hydroxybenzoates is preferred.

[0058] Component (C) can be used either alone or in combination of two or more. For example, benzyl alcohol and phenethyl alcohol are used in combination from (C1). Or, benzyl alcohol from (C1) and ethanol from (C2) are selected and used in combination. In order to improve the feeling of use, the ratio of (C1) to (C2) in component (C) can be The total amount is preferably 90% by mass or more, more preferably 95% by mass or more, and even more preferably 98% by mass or more. It is preferable that the content is substantially 100% by mass, and even more preferable that the content is substantially 100% by mass.

[0059] More specifically, the micelle formation of the epoxy aminosilane copolymer of component (A) is This suppresses the adhesion to fibers, providing sufficient hydrophobicity and low friction effects in a short time. Moreover, in order to maintain these effects for a long period after treatment, component (C) is ethanol. alcohol, benzyl alcohol, triethylene glycol, pentylene glycol, methyl propane Propanediol, phenoxyethanol, ethyl lactate, diethanolamine, guanidine At least one selected from the group consisting of ethanol, benzyl alcohol, phenoxyethanol, and the like is preferred. At least one selected from the group consisting of diethanol, ethyl lactate, diethanolamine, and guanidine salts One of these is more preferred, and is selected from ethanol, benzyl alcohol, and phenoxyethanol. It is more preferable to use at least one of the following.

[0060] The content of component (C) in the fiber treatment composition of the present invention is determined based on the hydrophobicity imparting effect on fibers. From the viewpoint of achieving a satisfactory result and maintaining the low friction effect for a long period of time, the content is preferably 5.0 mass % or more, more preferably Preferably 6.0% by mass or more, more preferably 7.0% by mass or more, even more preferably 10.0% by mass or more, The content is preferably 12.0% by mass or more, more preferably 15.0% by mass or more, and the storage stability is also good. From the viewpoint of increasing the content, it is preferably 96.8% by mass or less, more preferably 95.0% by mass or less, and even more preferably Preferably 90.0% by mass or less, more preferably 80.0% by mass or less, and even more preferably 70.0% by mass or less. The content is preferably 60.0 mass % or less, and more preferably 60.0 mass % or less.

[0061] In addition, the mass ratio of component (C) to the epoxyaminosilane copolymer (C) / epoxyamino From the viewpoint of fully exerting the micelle formation inhibiting effect, the silane copolymer preferably contains 1 or more more preferably 5 or more, even more preferably 6 or more, and even more preferably 7 or more, From the viewpoint of enhancing storage stability, the molecular weight is preferably 2000 or less, more preferably 1000 or less, and even more preferably 1000 or less. It is preferably 500 or less, and even more preferably 200 or less.

[0062] 〔water〕 The fiber treatment composition of the present invention preferably contains water as a solvent. The content of water in the agent composition is preferably 10 mass % from the viewpoint of facilitating application to fibers. % or more, more preferably 15% by mass or more, and even more preferably 20% by mass or more. From the viewpoint of facilitating subsequent drying of the fibers, the amount is preferably 90% by mass or less, more preferably 85% by mass or less. % or less, and more preferably 80% by mass or less.

[0063] [pH, pH adjuster] The pH of the fiber treatment composition of the present invention is adjusted to the tri- or tri-basic range of the component (A). From the viewpoint of increasing the reaction rate of the alkoxysilane moiety, the following ranges are preferred. When the pharmaceutical composition is in the acidic range, the pH is preferably 1 or more, more preferably 1.5 or more, and even more preferably 1.5 or more. Preferably, it is 2 or more, preferably 5 or less, more preferably 4.0 or less, and even more preferably In addition, when the fiber treatment composition of the present invention is in the basic region, it is preferable that It is preferably 7 or more, more preferably 7.5 or more, even more preferably 8.0 or more, and more preferably 11 or more. The fiber treatment composition of the present invention has a viscosity of 1000 MPa or less, more preferably 10.5 or less, and even more preferably 10 or less. In order to adjust the pH to the above range, the fiber treatment composition of the present invention contains an appropriate pH adjuster. As a pH adjuster, alkaline agents such as monoethanolamine and isoethanolamine can be used. Alkalis such as propanolamine, 2-amino-2-methylpropanol, and 2-aminobutanol alkanediamines such as 1,3-propanediamine or their salts; carbonates Guanidine, sodium carbonate, potassium carbonate, sodium bicarbonate, potassium bicarbonate, etc. and hydroxides such as sodium hydroxide and potassium hydroxide. In addition, examples of acidic agents include inorganic acids such as hydrochloric acid and phosphoric acid, hydrochlorides such as monoethanolamine hydrochloride, and phosphates. Phosphates such as monopotassium dihydrogen phosphate and disodium monohydrogen phosphate, lactic acid, malic acid, succinic acid Organic acids such as carboxylic acids can be used.

[0064] [Optional ingredients] In addition to the above components, the fiber treatment composition of the present invention may contain other components that are typically found in fiber treatment compositions. It can contain ingredients as needed, such as anti-dandruff agents, vitamins, and disinfectants. Anti-inflammatory agents, preservatives, chelating agents, moisturizing agents, dyes, pigments, and other coloring agents, extracts, pearlizing agents Agents; Fragrances; UV absorbers; Antioxidants; Photocatalysts; Shea butter; Rose water; Sunflower oil; Examples include range oil, eucalyptus oil, surfactants, etc. Photocatalysts include titanium dioxide, Metal oxides such as tungsten, 8-hydroxyquinoline, 7-cyano-2-naphthol, 8-quino Aromatic hydroxy compounds such as linoleic acid-1-oxide, other sulfonated pyrene compounds, nium salts, diazomethane derivatives, bissulfone derivatives, disulfonate derivatives, nitrobenzene sulfonate derivatives, sulfonate ester derivatives, sulfonate esters of N-hydroxyimides Examples of surfactants include cationic surfactants and anionic surfactants. Any of surfactants, amphoteric surfactants and nonionic surfactants can be used. Examples of the surfactant include alkylamine salts and alkyl quaternary ammonium salts. The anionic surfactants include alkyl sulfonates, alkyl carboxylates, and alkyl esters. alkyl ether sulfonates, alkyl ether carboxylates, etc., and amphoteric surfactants The antibacterial agents include imidazoline, carbobetaine, amidobetaine, sulfobetaine, and hydrobetaine. Examples of nonionic surfactants include hydroxysulfobetaine and amidosulfobetaine. Examples include glycerin fatty acid esters, sorbitan fatty acid esters, and sucrose fatty acid esters. esters, polyoxyethylene alkyl ethers, polyoxyethylene alkyl phenes Nyl ether, polyoxyethylene-polyoxypropylene alkyl ether, polyoxyethylene Examples include ethers such as diethylene polyoxypropylene alkyl phenyl ether. can be done.

[0065] Specifically, polyols such as propylene glycol and glycerin are used for moisturizing purposes. The content of these components in the fiber treatment composition of the present invention is preferably It is preferably 20% by mass or less, more preferably 10% by mass or less, and even more preferably 5% by mass or less. In addition, the amount of the photocatalyst in the fiber treatment composition of the present invention is set to a level that maintains the storage stability of the cosmetic. From the viewpoint of maintaining the above-mentioned content, it is preferably 2% by mass or less, more preferably 1% by mass or less, and even more preferably The content of the fiber treatment agent of the present invention is 0.1% by weight or less, and more preferably substantially 0% by weight. The amount of surfactant in the composition is preferably 2% or less from the viewpoint of maintaining the durability of the effect. % by mass or less, more preferably 1% by mass or less, even more preferably 0.1% by weight or less, and even more preferably Or it is substantially 0 mass %.

[0066] [Dosage form, etc.] The fiber treatment composition of the present invention may be in the form of, for example, a liquid, emulsion, cream, gel, or paint. It can be made into paste, mousse, aerosol, etc., but it is important to increase the drying speed and form a coating. From the viewpoint of facilitating the formation, the product must be in the form of a liquid, gel, paste, mousse, or aerosol. In the case of making it into an aerosol, the content of each component and the fiber treatment described above are preferably The pH of the agent composition is the content in the concentrate, ie, the pH of the concentrate, excluding the propellant.

[0067] [Fiber to be treated] Fibers to be treated with the fiber treatment composition of the present invention include keratin fibers such as hair. Examples include textile products such as fibers, cloth, and clothing, but hair is preferred.

[0068] [How to use] The fiber treatment composition of the present invention can be applied to fibers and then washed off, but does not wash off. It may be used by applying it to the fabric and then drying it without rinsing it off. It is preferable to use the above in order to further exhibit the effects of the present invention.

[0069] The amount of the fiber treatment composition of the present invention applied to the fiber is determined by the liquor ratio (fiber treatment The mass of the agent composition / the mass of the fiber is preferably 0.001 or more, more preferably 0.005 or more, It is preferably 0.01 or more, and is preferably 100 or less, more preferably 10 or less, and even more preferably Preferably it is 1 or less.

[0070] Furthermore, in the present invention, the composition containing component (A) is applied to the surface of a fiber and then dried. a composition containing component (B) is applied to the area to be treated, and then the composition is dried without rinsing. Alternatively, a composition containing component (B) can be applied to the surface of a fiber. Then, without drying, a composition containing component (A) is applied to the area to be treated, and the composition is left to stand for 1 hour without rinsing. The fiber treatment can also be carried out by drying the fiber.

[0071] In these cases, the content of component (A) in the composition containing component (A), component (B) The content of component (B) in the composition containing the above-mentioned fiber treatment composition of the present invention is The content of component (A) or component (B) in these compositions can be the same as that in the above. The fiber may contain water as a solvent and may further contain component (C) and other components. The amounts of these compositions to be applied may be the same as the liquor ratios described above.

[0072] With respect to the above-described embodiment, further preferred aspects of the present invention will be disclosed below.

[0073] <1> It contains the following components (A) and (B), and the content of component (A) is 0.05 mass% or more and 5.0 mass% or less. The content of component (B) is 0.05% by mass or more and 10.0% by mass or less, and the mass ratio of component (B) to component (A) is (B) / A fiber treatment composition in which (A) is 150 or less. (A) Self-crosslinking compound (B) Non-volatile silicone, polyhydric alcohol polymer, fatty acid ester and acrylic resin one or more color deepening agents selected from the group consisting of (excluding those corresponding to component (A))

[0074] <2> The fiber treatment composition according to <1>, wherein the component (A) is preferably one or more selected from the group consisting of the following components (A1) to (A3): (A1) Alkoxysilyl group-containing silicone (A2) Alkoxysilyl group-containing acrylate compound (A3) Alkoxysilyl group-containing alkylamine

[0075] <3> Component (A1) preferably comprises an alkoxysilyl group -SiR 1 n (OR 2 ) 3-n [In the formula, R 1 and R 2 each independently represents a monovalent hydrocarbon group, and n represents a number from 0 to 2. is a silicone bonded to an organopolysiloxane residue <2> The fiber treatment agent composition according to Finished product.

[0076] <4> Component (A1) is preferably an epoxyaminosilane which is a reaction product of the following compounds (a) to (d): It is a copolymer <3> The fiber treatment composition according to claim 1. (a) Polysiloxanes containing at least two oxiranyl or oxetanyl groups (b) Polyethers containing at least two oxiranyl or oxetanyl groups (c) Aminopropyltrialkoxysilane (d) Compounds selected from the group consisting of the following primary and secondary amines: Primary amines: methylamine, ethylamine, propyleneamine, ethanolamine, Isopropylamine, butylamine, isobutylamine, hexylamine, dodecylamine amine, oleylamine, aniline, aminopropyltrimethylsilane, aminopropyltrimethylsilane Ethylsilane, aminomorpholine, aminopropyldiethylamine, benzylamine, Butylamine, 3-amino-9-ethylcarbazole, 1-aminoheptafluorohexane, 2,2,3 ,3,4,4,5,5,6,6,7,7,8,8,8-Pentadecafluoro-1-octanamine Secondary amines: methylethylamine, methyloctadecylamine, diethanolamine , dibenzylamine, dihexylamine, dicyclohexylamine, piperidine, pyrolyl Diphthalimide, polymer amine

[0077] <5> The compound (a) is preferably represented by the following general formula (1): <4> Fiber treatment according to Agent composition.

[0078] [ka]

[0079] [wherein R has an oxiranyl group or an oxetanyl group at the terminal, and may contain a heteroatom] represents a hydrocarbon group having 1 to 6 carbon atoms, and x represents a number from 1 to 1000.

[0080] <6> The compound (b) is preferably represented by the following general formula (2): <4> or <5> Described in A fiber treatment composition.

[0081] [ka]

[0082] [wherein R has the same meaning as above, y is 1 to 100, z is 0 to 100, and y+z is 1 to 20] Indicates a number that is 0.]

[0083] <7> The compound (c) is preferably aminopropyltrimethoxysilane, aminopropyltriethoxysilane, Triisopropoxysilane, Aminopropyltripropoxysilane, Aminopropyltriisopropoxysilane Silane, aminopropyl tributoxysilane and aminopropyl tri-tert-butoxysilane At least one species selected from the group consisting of orchids <4> ~ <6> described in any one of the following items A fiber treatment composition.

[0084] <8> Compound (d) is preferably a primary amine, more preferably aminopropyldiethylamine. aminopropyl dimethylamine and aminopropyl dibutylamine At most one species <4> ~ <7> The fiber treatment composition according to any one of the preceding claims.

[0085] <9> Component (A1) is preferably polysilicone-29 <4> ~ <8> Any one of the following items The fiber treatment composition described above.

[0086] <10> Component (A1) is preferably (amodimethicone / morpholinomethylsilsesquioxane) copolymer. It is a polymer <3> The fiber treatment composition according to claim 1.

[0087] <11> Component (A2) is preferably an alkoxysilyl group -SiR 1 n (OR 2 ) 3-n [In the formula, R 1 and R 2each independently represents a monovalent hydrocarbon group, and n represents a number from 0 to 2. is represented by the following general formula (3)

[0088] [ka]

[0089] [In the formula, R 3 represents a hydrogen atom or a methyl group, and R 4 is a divalent saturated hydrocarbon group having 1 to 6 carbon atoms indicates.] is a compound bonded to a group represented by <2> The fiber treatment composition according to claim 1.

[0090] <12> Component (A2) is preferably 3-methacryloxypropylmethyldimethoxysilane, 3-methacryloxypropylmethyldimethoxysilane. Acryloxypropyltrimethoxysilane, 3-methacryloxypropylmethyldiethoxysilane silane, 3-methacryloxypropyltriethoxysilane and 3-acryloxypropyltrimethoxysilane A silane coupling agent selected from the group consisting of silanes <11> Fiber treatment according to Agent composition.

[0091] <13> Component (A3) is preferably an alkoxysilyl group -SiR 1 n (OR 2 ) 3-n [In the formula, R 1 and R 2 each independently represents a monovalent hydrocarbon group, and n represents a number from 0 to 2. is represented by the following general formula (4)

[0092] [ka]

[0093] [In the formula, R 5 and R 6represents a hydrocarbon group which may be substituted with a hydrogen atom or an amino group. or they may together form an alkylidene group, R 7 is a divalent carbon atom with 1 to 6 carbon atoms represents a hydrocarbon group. is a compound bonded to a group represented by <2> The fiber treatment composition according to claim 1.

[0094] <14> Component (A3) is preferably N-2-(aminoethyl)-3-aminopropylmethyldimethoxysilane N-2-(aminoethyl)-3-aminopropyltrimethoxysilane, 3-aminopropyltrimethoxysilane Methoxysilane, 3-aminopropyltriethoxysilane, 3-triethoxysilyl-N-(1,3- Dimethyl-butylidene)propylamine, N-phenyl-3-aminopropyltrimethoxysilane N-(vinylbenzyl)-2-aminoethyl-3-aminopropyltrimethoxysilane hydrochloride At least one selected from the group consisting of, more preferably, 3-aminopropyl-triethoxy Silane, 3-aminopropylmethyldiethoxysilane, N-(2-aminoethyl)-3-aminopropyl Propyltriethoxysilane and 3-(2-aminoethylamino)propylmethyldiethoxysilane At least one selected from the group consisting of <13> The fiber treatment composition according to claim 1.

[0095] <15> The content of component (A) is preferably 0.1% by mass or more, more preferably 0.2% by mass or more, and further It is preferably 0.25% by mass or more, and more preferably 3.0% by mass or less, and more preferably 1.0% by mass or less. % by mass or less, more preferably 0.5% by mass or less <1> ~ <14> described in any one of the following items A fiber treatment composition.

[0096] <16> Component (B) is preferably dimethylpolysiloxane, amino-modified polysiloxane, phenyl modified polysiloxane, polyglycerin modified polysiloxane, silicone resin, acrylic alkyl-modified polysiloxane, alkyl-modified polysiloxane, methacrylic-modified polysiloxane, Carboxyl-modified polysiloxane, aminopolyether-modified polysiloxane, oxazolidinyl Polyether-modified polysiloxane, fluorine-modified polysiloxane, Mercapto-modified polysiloxane, hydrogen-modified polysiloxane, aralkyl-modified polysiloxane polysiloxane, epoxy-modified polysiloxane, and hydroxy-modified polysiloxane. At least one non-volatile silicone <1> ~ <15> The fiber according to any one of claims 1 to 5 Fiber treatment composition.

[0097] <17> Component (B) is preferably diethylene glycol, dipropylene glycol, triethylene glycol Glycol, Polypropylene Glycol, Tetraethylene Glycol, Diglycerin, Polyethylene Glycol polyethylene glycol, triglycerin, tetraglycerin and polyglycerin At least one polyhydric alcohol polymer <1> ~ <15> described in any one of the following items A fiber treatment composition.

[0098] <18> Component (B) is preferably a lauric acid ester, a myristate ester, a palmitate ester, or Ester, oleate, phthalate, adipate, caprylate esters, capric acid esters, behenic acid esters, methacrylic acid esters and ethylhexyl At least one fatty acid ester selected from the group consisting of carboxylic acid esters <1> ~ <15> Noi The fiber treatment composition according to any one of the above.

[0099] <19> The alcohol component in the fatty acid ester is preferably methanol, ethanol, or Panol, butanol, pentanol, hexanol, heptanol, octanol, decanol Canol, 2-ethylhexanol, lauryl alcohol, myristyl alcohol, ethyl alcohol, stearyl alcohol, isostearyl alcohol, oleyl alcohol behenyl alcohol, isopropyl alcohol, isobutyl alcohol, isodecyl Alcohol, ethylene glycol, propylene glycol, butylene glycol, diethylene ethylene glycol, triethylene glycol, glycerin, trimethylolpropane, tri Ethanolamine, pentaerythritol, diglycerin, xylose, sorbitan, Citrate, triglyceride, glucose, fructose, sorbitol, malbitol, tetraglyceride Glycerin, polyglycerol with more than six hydroxyl groups, sucrose, trehalose, lactose and maltotriose. <18> The fiber treatment agent according to composition.

[0100] <20> The component (B) is preferably a polymer containing a repeating unit represented by the following general formula (5): <15> The fiber treatment composition according to any one of the preceding claims.

[0101] [ka]

[0102] [In the formula, R 8 represents a hydrogen atom, a methyl group, or an ethyl group, and X 1 represents an oxygen atom or an imino group. And X1 When is an oxygen atom, -Y 1 -X 2 is a hydrogen atom, and is an alkyl group with 1 to 24 carbon atoms. alkyl group, isobornyl group, -(CH2) p -N(R 9 )2, -(CH2) p -N + (R 9 )3, -(CH2) p -OR 9 , -C(CH3)2-N(R 9 )2 or -C(CH3)2-OR 9 (p is a number between 1 and 3. and R 9 represents a hydrogen atom or an alkyl group having 1 to 4 carbon atoms), or Y 1 represents a group consisting of an oxyethylene group and / or an oxypropylene group, and X 2 Water represents a hydrogen atom, a methyl group, or an ethyl group, and X 1 If is NH, then Y 1 is a compound with 1 to 3 carbon atoms represents the following divalent saturated hydrocarbon group, and X 2 -N(R 9 )2(R 9 indicates the same as above) . ]

[0103] <21> Component (B) is preferably poly(methacryloyloxyethyltrimethylammonium chloride). Polyquaternium-37 (INCI name: Polyquaternium-37), vinylpyrrolidone·N,N-dimethylamino Diethyl methacrylic acid copolymer diethyl sulfate (INCI name: Polyquaternium-11) and acrylic acid copolymer Rates / C 1-18 Alkyl acrylates / C 1-8 Select from alkyl acrylamide copolymers At least one species is revealed <20> The fiber treatment composition according to claim 1.

[0104] <22> Component (B) is preferably polysilicone-9, polyquaternium-37 and polyethylene glycol. At least one species selected from the group <1> ~ <21> The fiber processing method according to any one of claims 1 to 4, Pharmacological composition.

[0105] <23> The content of component (B) is preferably 0.5% by mass or more, more preferably 1.0% by mass or more, and further It is preferably 1.5% by mass or more, and is preferably 7.0% by mass or less, and more preferably 5.0% by mass or less. % by mass or less, more preferably 2.5% by mass or less <1> ~ <22> described in any one of the following items A fiber treatment composition.

[0106] <24> the mass ratio (B) / (A) of component (B) to component (A) is 150 or less, preferably 100 or less; More preferably, it is 10 or less, and also preferably 0.05 or more, more preferably 3 or more. <1> ~ <23> The fiber treatment composition according to any one of the preceding claims.

[0107] <25> Preferably, at least one micelle formation inhibitor selected from the following (C1) to (C3) is further included: Contains <4> ~ <9> The fiber treatment composition according to any one of the preceding claims. (C1): The hydrogen bond term of the Hansen solubility parameter is 10.0 MPa 1 / 2 Over 15.8MPa 1 / 2 Below Certain organic compounds (excluding those falling under (C3)) (C2): Ethanol, triethylene glycol, pentylene glycol, methylpropional a compound selected from diethanolamine, diethanolamine, and N-methyldiethanolamine (C3): Organic salt

[0108] <26> Component (C1) is preferably 1-propanol, 2-propanol, 1-butanol, 2-butanol alcohol, hexylene glycol, octanediol, decanediol, benzyl alcohol , cinnamyl alcohol, phenethyl alcohol, p-anisyl alcohol, p-methylbenzyl alcohol Diethyl alcohol, phenoxyethanol, 2-benzyloxyethanol, 2-phenyl-1- Propanol, ethylene glycol monoethyl ether, ethylene glycol monobutyl Ether, Diethylene Glycol Monomethyl Ether, Diethylene Glycol Monoethyl Ether, Diethylene Glycol Monobutyl Ether, Ethylhexyl Glyceryl Ether N-(2-hydroxyethyl)-2-pyrrolidone, ethyl lactate, butyl lactate, methylamine, Selected from ethylamine, N,N-dimethylmonoethanolamine and aminomethylpropanol More preferably, benzyl alcohol, phenethyl alcohol, At least one selected from phenoxyethanol and 2-benzyloxyethanol R <25> The fiber treatment composition according to claim 1.

[0109] <27> Component (C3) is preferably a guanidine salt having a guanidinium group and an arginine salt. At least one selected from the group consisting of guanidine hydrochloride, guanidine nitrate, and guanidine nitrate is preferred. Guanidine phosphate, guanidine thiocyanate, guanidine carbonate, guanidine acetate, guanidine Aminoguanidine sulfate, guanidine sulfamate, aminoguanidine hydrochloride, aminoguanidine Arginine sulfate, arginine hydrochloride, arginine nitrate, arginine phosphate, arginine thiosulfate Cyanate, arginine carbonate, arginine acetate, arginine sulfate, arginine sulfate arginine glutamate, arginine aspartate, At least one of the following <25> The fiber treatment composition according to claim 1.

[0110] <28> The total amount of (C1) and (C2) in component (C) is preferably 90% by mass or more, more preferably 95% by mass or more. More preferably, it is 98% by mass or more, and even more preferably, it is substantially 100% by mass. <25> ~ <27> The fiber treatment composition according to any one of the preceding claims.

[0111] <29> The content of component (C) is preferably 5.0% by mass or more, more preferably 6.0% by mass or more, and further Preferably 7.0% by mass or more, more preferably 10.0% by mass or more, and even more preferably 12.0% by mass It is more preferably 15.0 mass % or more, and more preferably 96.8 mass % or less, and even more preferably Preferably 95.0% by mass or less, more preferably 90.0% by mass or less, and even more preferably 80.0% by mass or less. More preferably, the content is 70.0% by mass or less, and even more preferably, 60.0% by mass or less. <25> <28> The fiber treatment composition according to any one of the above items.

[0112] <30> Mass ratio of component (C) to epoxyaminosilane copolymer (C) / epoxyaminosilane The copolymer preferably has 1 or more, more preferably 5 or more, even more preferably 6 or more, More preferably, it is 7 or more, and also preferably 2000 or less, more preferably 1000 or less, and further preferably Preferably, it is 500 or less, and more preferably, it is 200 or less. <25> ~ <29> Any one of the following items The fiber treatment composition described above.

[0113] <31> The pH is preferably 1 or more, more preferably 1.5 or more, and even more preferably 2 or more, Preferably it is 5 or less, more preferably 4.0 or less, and even more preferably 3.5 or less. <1> <30> The fiber treatment composition according to any one of the above items.

[0114] <32> The pH is preferably 7 or higher, more preferably 7.5 or higher, and even more preferably 8.0 or higher; Preferably it is 11 or less, more preferably 10.5 or less, and even more preferably 10 or less. <1> <30> The fiber treatment composition according to any one of the above items.

[0115] <33> <1> ~ <32> After applying the fiber treatment composition according to any one of the above to the surface of a fiber, the fiber treatment composition is washed off. A textile treatment method that dries textiles without drying.

[0116] <34> The amount of fiber treatment composition applied to the fiber is determined by the liquor ratio (fiber treatment composition The mass of the fiber / mass of the fiber is preferably 0.001 or more, more preferably 0.005 or more, and even more preferably It is preferably 0.01 or more, and is preferably 100 or less, more preferably 10 or less, and even more preferably is less than or equal to 1 <33> The fiber treatment method according to claim 1.

[0117] <35> A composition containing the following component (A) is applied to the surface of a fiber, and then the applied portion is left without drying. A textile treatment method comprising applying a composition containing the following component (B) to textiles and then drying the textiles without rinsing. (A) Self-crosslinking compound (B) Non-volatile silicone, polyhydric alcohol polymer, fatty acid ester and acrylic resin one or more color deepening agents selected from the group consisting of (excluding those corresponding to component (A))

[0118] <36> A composition containing the following component (B) is applied to the surface of a fiber, and then the applied portion is left to dry. A textile treatment method comprising applying a composition containing the following component (A) to textiles and then drying the textiles without rinsing them off. (A) Self-crosslinking compound (B) Non-volatile silicone, polyhydric alcohol polymer, fatty acid ester and acrylic resin one or more color deepening agents selected from the group consisting of (excluding those corresponding to component (A))

[0119] <37> It contains the following components (A) and (B), and the content of component (A) is 0.25 mass% or more and 0.5 mass% or less. A fiber treatment composition having a content of component (B) of 1.5% by mass or more and 2.5% by mass or less. (A) Polysilicone-29 (B) Polysilicone-9

[0120] <38> It contains the following components (A) and (B), and the content of component (A) is 0.25 mass% or more and 0.5 mass% or less. A fiber treatment composition having a content of component (B) of 1.5% by mass or more and 2.5% by mass or less. (A) Polysilicone-29 (B) Polyquaternium-37

[0121] <39> It contains the following components (A) and (B), and the content of component (A) is 0.25 mass% or more and 0.5 mass% or less. A fiber treatment composition having a content of component (B) of 1.5% by mass or more and 2.5% by mass or less. (A) Polysilicone-29 (B) Polyethylene glycol [Example]

[0122] Examples 1 to 16, Comparative Examples 1 to 7 Aqueous solutions having the compositions shown in Tables 1 to 3 were prepared, and the film-forming properties of these solutions and their application to hair were evaluated. The darkening effect and durability of the coating were evaluated.

[0123] (Preparation method for each aqueous solution) In a 200 mL beaker containing a stirrer, measure out the specified amounts of purified water and each component listed in Table 1. Stir and mix for at least 30 minutes using a stirring rod until the aqueous solution becomes homogeneous.

[0124] (Film-forming property evaluation method) Drop 300 μL of each solution onto a glass slide and dry it in an oven set at 90°C for 30 minutes. After that, leave it at room temperature for about 10 minutes, and then check whether a film has formed by visual and sensory evaluation. A dry, smooth film that is not sticky and does not stick to the hands is rated as "5: Very good", and a non-sticky film is rated as "6: Very good". A dry film that is smooth and does not stick to the hands is rated as "4: Good," and a dry film that is slightly sticky is rated as "3: Average." A film that is partially dry is rated as "2: Poor," a film that is mostly dry is rated as "1: Good," a film that is partially dry is rated as "2: Poor," and a film that is mostly dry is rated as "1: Poor." The results were rated on a 5-point scale, with the rating being "very bad."

[0125] (Darkening effect evaluation method) All the hair samples used for evaluation were healthy Caucasian hair (3.0g) with tresses and powder bleach (GOLDWELL Damaged hair that had been treated once with TOPCHIC was used. Each solution shown in Tables 1 to 3 was applied evenly to the wet tresses after rinsing with water at a bath ratio of 0.2. (A separate trace was used for each solution) and then completely dried with a hair dryer without rinsing. After that, wash with the plain shampoo shown below and dry. This process was repeated a total of three times.

[0126] Plain shampoo (pH 6.9) composition (mass%) Polyoxyethylene lauryl ether sodium sulfate (Emar 170J, manufactured by Kao Corporation, active ingredient 70% by mass) 13.0 Coconut oil fatty acid monoethanolamide (Amizol CME, manufactured by Kawaken Fine Chemicals Co., Ltd.) 0.6 Coconut oil fatty acid amidopropyl carbobetaine (Amphitol 55AB, manufactured by Kao Corporation, active ingredient 30% by mass) 1.41 Citric acid pH adjustment amount Sodium benzoate 0.3 Remaining purified water

[0127] For each tress after powder bleaching, a color difference meter was used before and after treatment with the aqueous solution. The Lab value, a color index, was measured. The color difference meter used was the Konica Minolta CR-400. Set the temperature to 80℃ and use a straightening iron for 5 strokes at a speed of 3 seconds per stroke. The measurement was performed with the surface straight. The measured L value was used to compare the The larger the negative difference (ΔL) in the L value after treatment, the greater the darkening effect, and ΔL of 2.5 or more is considered to be "5: Very high", ΔL less than 2.5 and 1.5 or more is "4: High", ΔL less than 1.5 and 1.0 or more is " 3: Normal, ΔL less than 1.0 and 0.5 or more is "2: Low", ΔL less than 0.5 is "1: Very Low" " and rated on a 5-point scale.

[0128] (Method for evaluating film durability) All the hair samples used for evaluation were 1.0 g tresses of healthy Japanese hair. Wet the tresses with water and towel-dried them, then apply each of the solutions shown in Table 1 or 2 at a bath ratio of 0.01 to the hair. 3 and then dried completely using a hairdryer without rinsing. The hair was washed once with shampoo and then completely dried using a hair dryer. Sensory evaluation was performed on the tresses before and after shampooing and when they were dried, and the difference in texture was compared. If the feel remains the same even after shampooing and there is no tangling from the middle to the ends of the hair, then it is rated as "A". Those that felt a slight grip were rated "B", and those that felt a grip were rated "C".

[0129] [Table 1]

[0130] [Table 2]

[0131] [Table 3]

[0132] Formulation example 1 (leave-in fabric treatment gel; pH 3.5) (mass %; all active ingredients) Epoxy Amino Silane Copolymer (Silsoft CLX-E, manufactured by Momentive, active ingredient 15% by mass) 3.0 Ethanol 30.0 Poly(methacryloyloxyethyltrimethylammonium chloride) (Cosmedia Ultra Gel 300 (BASF) 1.00 Lactic acid pH adjustment amount Water remainder (*10) *10: Contains water and dipropylene glycol derived from Silsoft CLX-E

[0133] Formulation Example 2 (Leave-in fabric treatment lotion; pH 3.5) (% by mass; all active ingredients) 3-Acryloxypropyltrimethoxysilane (KBM-5103; Shin-Etsu Chemical Co., Ltd.) 3.0 Ethanol 30.0 Poly(methacryloyloxyethyltrimethylammonium chloride) (Cosmedia Ultra Gel 300 (BASF) 0.50 Lactic acid pH adjustment Water Remnants

Claims

1. Contains the following components (A) and (B): The content of component (A) is 0.05% by mass or more and 5.0% by mass or less, The content of component (B) is 0.05% by mass or more and 10.0% by mass or less, the mass ratio (B) / (A) of the component (B) to the component (A) is 3 or more and 10 or less; Fiber treatment composition. (A) one or more self-crosslinking compounds selected from the group consisting of the following components (A1) and (A3): (A1) An epoxyaminosilane copolymer which is a reaction product of the following compounds (a) to (d): (a) A polysiloxane having at least two oxiranyl or oxetanyl groups, represented by the following general formula (1): 【Chemical 1】 [In the formula, R represents a hydrocarbon group having 1 to 6 carbon atoms and an oxiranyl group or an oxetanyl group at its terminal, which may contain a heterooxygen atom, and x represents a number from 1 to 1,000.] (b) A polyether having at least two oxiranyl or oxetanyl groups, represented by the following general formula (2): 【Chemistry 2】 [In the formula, R has the same meaning as above, y is a number from 1 to 100, z is a number from 0 to 100, and y+z is a number from 1 to 200.] (c) Aminopropyltrialkoxysilane (d) aminopropyldiethylamine (A3) Alkoxysilyl group-containing alkylamine (B) A color deepening agent containing polyquaternium-37

2. The fiber treatment composition according to claim 1 , which has a pH of 1 or more and 5 or less, or 7 or more and 11 or less.

3. 3. The fiber treatment composition according to claim 1, wherein component (A1) is polysilicone-29.

4. The fiber treatment composition according to any one of claims 1 to 3, further comprising, as component (C), at least one micelle formation inhibitor selected from ethanol, hexylene glycol, and dipropylene glycol.

5. The fiber treatment composition according to claim 4, wherein the content of the micelle formation inhibitor is 5.0% by mass or more and 96.8% by mass or less.

6. A method for treating fibers, comprising applying the fiber treating composition according to any one of claims 1 to 5 to a surface of a fiber and then drying the same without rinsing it off.

Citation Information

Patent Citations

  • Hair coloring composition for providing a film on keratin fibers

    EP3281623A1

  • Method for enhancing chroma of hair

    JP2006206585A