Dye composition for regenerated collagen fibers

Abstract

To provide a dyeing agent composition for a regenerated collagen fiber using a dye and excellent in fastness of the regenerated collagen fiber.SOLUTION: A dye composition for regenerated collagen fibers, which is used by mixing at least a first agent and a second agent at the time of use, wherein the first agent contains a specific oxidation dye intermediate (A), an alkali agent, and water, the second agent contains hydrogen peroxide and water, and the regenerated collagen fibers include modified regenerated collagen fibers containing a specific compound (B).SELECTED DRAWING: None

Description

[Technical Field]

[0001] The present invention relates to a dye composition for use on regenerated collagen fibers. [Background technology]

[0002] Regenerated collagen fiber, a protein fiber, is suitable for use as a raw material for artificial hair because its properties are similar to those of human hair. Fibers used as raw materials for artificial hair must have high aesthetic qualities, such as color development and texture.

[0003] Protein fibers are generally colored by a dyeing method in which the protein fibers are immersed in an aqueous dye solution maintained at 70 to 100°C. For example, Patent Document 1 describes a dyeing method in which wool is immersed in an aqueous dye solution containing enzymes and the like to improve dye leveling, and then boiled at 100° C. for 60 minutes. Patent Document 2 describes a method for dyeing protein fibers such as wool, cashmere, and silk threads at a temperature of 70 to 90°C, which is lower than conventional dyeing temperatures, by using a specific treating agent. The example also discloses an example in which wool is treated with a specific treating agent and then dyed at a dyeing temperature of 85°C. [Prior art documents] [Patent documents]

[0004] [Patent Document 1] Japanese Patent Application Publication No. 2-216282 [Patent Document 2] Japanese Patent Application Publication No. 7-126988 Summary of the Invention [Problem to be solved by the invention]

[0005] In conventional general dyeing methods for protein fibers, such as those disclosed in Patent Documents 1 and 2, even when special treatment agents are used, the dye cannot be sufficiently absorbed unless treatment is performed at a high temperature exceeding 70° C. Furthermore, when regenerated collagen fibers are dyed using a dyeing method that requires high-temperature conditions exceeding 70° C., there is a problem in that the regenerated collagen fibers shrink.

[0006] In order to solve the above problems, the inventors attempted to dye regenerated collagen fibers at temperatures below 70°C. However, when the dyeing temperature was low, the chemical reaction between the regenerated collagen fibers and the dye became insufficient, resulting in a problem of reduced dye fastness.

[0007] Therefore, the only practical method for coloring regenerated collagen fibers is to disperse a pigment such as carbon black in the solution spinning process of the regenerated collagen fibers. However, with coloring methods using pigments, the range of colors that can be colored is limited to achromatic colors such as black and gray, as well as chromatic colors such as red, yellow, blue, and purple, but it is difficult to produce vivid colors such as deep black.

[0008] Therefore, the present invention relates to a dye composition for regenerated collagen fibers that uses a dye and provides excellent fastness to the regenerated collagen fibers. [Means for solving the problem]

[0009] The present inventors have discovered that a dye composition for regenerated collagen fibers, including specific modified regenerated collagen fibers, which uses a specific oxidative dye intermediate, can solve the above-mentioned problems. That is, the present invention relates to the following. [1] A dye composition for regenerated collagen fibers, which comprises a mixture of at least a first agent and a second agent, the first agent contains an oxidation dye intermediate (A) containing one or more selected from the group consisting of the following components (A1) and (A2), an alkaline agent, and water; the second agent contains hydrogen peroxide and water, The regenerated collagen fibers include modified regenerated collagen fibers containing one or more compounds (B) selected from the group consisting of the following components (B1) and (B2): Dyeing composition for regenerated collagen fibers.

[0010] (A1) One or more couplers selected from the group consisting of couplers (A1-1) having a benzene ring, electron-donating groups at the 1st and 3rd positions on the benzene ring, and hydrogen atoms at the 4th and 6th positions; couplers (A1-2) having a pyridine ring, electron-donating groups at the 2nd and 6th positions on the pyridine ring, and hydrogen atoms at the 3rd and 5th positions; and couplers (A1-3) represented by the following general formula (A13):

[0011] [ka]

[0012] (In formula (A13), R 11 is -O-(CH2) n R is a divalent group represented by -O- (n is a number of 2 or more and 10 or less). 12 , R 14 , R 22 and R 24 is an electron-donating group, and R 15 and R 25 is a hydrogen atom. R 13 , R 16 , R 23 and R 26 are each independently a hydrogen atom, an alkyl group, or an electron-donating group.

[0013] (A2) One or more couplers other than the component (A1), selected from the group consisting of couplers (A2-1) having a benzene ring, electron-donating groups at the 1st and 2nd positions on the benzene ring, and hydrogen atoms at two or more of the 3rd to 6th positions, and couplers (A2-2) having a pyridine ring, electron-donating groups at the 2nd and 3rd positions on the pyridine ring, and hydrogen atoms at two or more of the 4th to 6th positions.

[0014] (B1) Benzoic acid or its salts (B2) A copolymer containing a structural unit derived from an unsaturated monomer having a carboxy group and a structural unit derived from an aromatic vinyl compound, the copolymer having an acid value of 100 mgKOH / g or more and a weight average molecular weight of 1500 or more and 15000 or less, or a salt thereof.

[0015] [2] A method for dyeing regenerated collagen fibers, comprising: The dyeing method includes the following steps (I) and (II) in this order: The regenerated collagen fibers include modified regenerated collagen fibers containing one or more compounds (B) selected from the group consisting of the component (B1) and the component (B2). A method for dyeing regenerated collagen fibers.

[0016] Process (I) A step of mixing at least the first agent and the second agent to prepare a dye composition for regenerated collagen fibers. Here, the first agent contains the oxidative dye intermediate (A) containing one or more selected from the group consisting of the component (A1) and the component (A2), an alkaline agent, and water, and the second agent contains hydrogen peroxide and water. Process (II) applying the regenerated collagen fiber dye composition to the regenerated collagen fiber;

[0017] [3] Colored modified regenerated collagen fiber containing the following component (A0) and component (B): (A0) A reaction product of the oxidation dye intermediate (A) containing one or more components selected from the group consisting of the component (A1) and the component (A2). (B) one or more compounds selected from the group consisting of the following components (B1) and (B2): (B1) Benzoic acid or its salts (B2) A copolymer containing a structural unit derived from an unsaturated monomer having a carboxy group and a structural unit derived from an aromatic vinyl compound, the copolymer having an acid value of 100 mgKOH / g or more and a weight average molecular weight of 1500 or more and 15000 or less, or a salt thereof. [4] A headwear product comprising the colored modified regenerated collagen fiber described in [3]. [Effects of the Invention]

[0018] According to the present invention, a dye composition for regenerated collagen fibers, which uses a dye and has excellent fastness for specific modified regenerated collagen fibers, can be provided. DETAILED DESCRIPTION OF THE INVENTION

[0019] [Definition] As used herein, "excellent dyeability of regenerated collagen fibers" means that there is a large change in color of regenerated collagen fibers before and after dyeing with a dye composition for regenerated collagen fibers. Furthermore, "fastness" means that there is little change in color of the dyed regenerated collagen fibers after washing with water, a detergent, etc. The dyeability and fastness can be specifically evaluated by the methods described in the examples.

[0020] [Dyeing composition for regenerated collagen fibers] The dye composition for regenerated collagen fibers of the present invention is a dye composition for regenerated collagen fibers that uses a mixture of at least a first agent and a second agent, the first agent contains an oxidation dye intermediate (A) containing one or more selected from the group consisting of the following components (A1) and (A2), an alkaline agent, and water; the second agent contains hydrogen peroxide and water, The regenerated collagen fibers include modified regenerated collagen fibers containing one or more compounds (B) selected from the group consisting of the following components (B1) and (B2):

[0021] (A1) One or more couplers selected from the group consisting of couplers (A1-1) having a benzene ring, electron-donating groups at the 1st and 3rd positions on the benzene ring, and hydrogen atoms at the 4th and 6th positions; couplers (A1-2) having a pyridine ring, electron-donating groups at the 2nd and 6th positions on the pyridine ring, and hydrogen atoms at the 3rd and 5th positions; and couplers (A1-3) represented by the following general formula (A13):

[0022] [ka]

[0023] (In formula (A13), R 11 is -O-(CH2) n R is a divalent group represented by -O- (n is a number of 2 or more and 10 or less). 12 , R 14 , R 22 and R 24 is an electron-donating group, and R 15 and R 25 is a hydrogen atom. R 13 , R 16 , R 23 and R 26 are each independently a hydrogen atom, an alkyl group, or an electron-donating group.

[0024] (A2) One or more couplers other than the component (A1), selected from the group consisting of couplers (A2-1) having a benzene ring, electron-donating groups at the 1st and 2nd positions on the benzene ring, and hydrogen atoms at two or more of the 3rd to 6th positions, and couplers (A2-2) having a pyridine ring, electron-donating groups at the 2nd and 3rd positions on the pyridine ring, and hydrogen atoms at two or more of the 4th to 6th positions.

[0025] (B1) Benzoic acid or its salts (B2) A copolymer containing a structural unit derived from an unsaturated monomer having a carboxy group and a structural unit derived from an aromatic vinyl compound, the copolymer having an acid value of 100 mgKOH / g or more and a weight average molecular weight of 1500 or more and 15000 or less, or a salt thereof.

[0026] In the following description, the dye composition for regenerated collagen fibers may be simply referred to as the "composition (of the present invention)." Since the composition of the present invention has the above-mentioned structure, even if it is a staining composition using a dye, it has excellent fastness for the specific modified regenerated collagen fibers.

[0027] The reason why the composition of the present invention exhibits the above-mentioned effects is not clear, but is presumed to be as follows. The composition of the present invention is a dye composition prepared by mixing a first agent containing an alkaline agent with a second agent containing hydrogen peroxide. The first agent contains, as a dye precursor, one or more specific oxidation dye intermediates selected from the group consisting of the above-mentioned components (A1) and (A2). The oxidative dye intermediate is a low-molecular-weight compound, and when a dye composition containing the oxidative dye intermediate is applied to regenerated collagen fibers, it easily penetrates into the fibers. The penetration of the oxidative dye intermediate into the fibers is promoted by the alkaline agent contained in the first agent. After penetrating into the fibers, the oxidative dye intermediate reacts with its couplers or with its precursor due to the action of hydrogen peroxide contained in the second agent to form a reaction product, which develops color and exhibits dyeability. Here, the oxidation dye intermediate (A1) used in the present invention is a coupler having a specific structure, and due to this structure, component (A1) easily forms a reaction product of a trimer or higher. Similarly, the coupler of component (A2) also easily forms a reaction product of a dimer or higher due to its specific structure. Therefore, when one or more oxidation dye intermediates selected from the group consisting of components (A1) and (A2) are used, high-molecular-weight reaction products are easily produced inside the fiber, which is thought to improve fastness.

[0028] Furthermore, the regenerated collagen fibers to be dyed with the composition of the present invention include modified regenerated collagen fibers (hereinafter simply referred to as "modified regenerated collagen fibers") containing one or more compounds (B) selected from the group consisting of the aforementioned components (B1) and (B2). Compound (B) acts as a modifier for the regenerated collagen fibers. Inside the modified regenerated collagen fibers, the structural moiety derived from compound (B) interacts with the specific oxidative dye intermediate and its reaction product, which is thought to facilitate retention of the oxidative dye intermediate and its reaction product inside the fibers without heat treatment, thereby further improving fastness. The mechanism of action of the present invention is not limited to the above.

[0029] <First agent> The first agent contains an oxidation dye intermediate (A) containing one or more members selected from the group consisting of the following components (A1) and (A2), an alkali agent, and water. (A1) One or more couplers selected from the group consisting of couplers (A1-1) having a benzene ring, electron-donating groups at the 1st and 3rd positions on the benzene ring, and hydrogen atoms at the 4th and 6th positions; couplers (A1-2) having a pyridine ring, electron-donating groups at the 2nd and 6th positions on the pyridine ring, and hydrogen atoms at the 3rd and 5th positions; and couplers (A1-3) represented by the following general formula (A13):

[0030] [ka]

[0031] (In formula (A13), R 11 is -O-(CH2) n R is a divalent group represented by -O- (n is a number of 2 or more and 10 or less). 12 , R 14 , R 22 and R 24 is an electron-donating group, and R 15 and R 25 is a hydrogen atom. R 13 , R 16 , R 23 and R 26 are each independently a hydrogen atom, an alkyl group, or an electron-donating group.

[0032] (A2) One or more couplers other than the component (A1), selected from the group consisting of couplers (A2-1) having a benzene ring, electron-donating groups at the 1st and 2nd positions on the benzene ring, and hydrogen atoms at two or more of the 3rd to 6th positions, and couplers (A2-2) having a pyridine ring, electron-donating groups at the 2nd and 3rd positions on the pyridine ring, and hydrogen atoms at two or more of the 4th to 6th positions.

[0033] (Oxidation dye intermediate (A)) The oxidation dye intermediate (A) contains one or more members selected from the group consisting of the following components (A1) and (A2): (A1) One or more couplers selected from the group consisting of couplers (A1-1) having a benzene ring, electron-donating groups at the 1st and 3rd positions on the benzene ring, and hydrogen atoms at the 4th and 6th positions; couplers (A1-2) having a pyridine ring, electron-donating groups at the 2nd and 6th positions on the pyridine ring, and hydrogen atoms at the 3rd and 5th positions; and couplers (A1-3) represented by the following general formula (A13):

[0034] [ka]

[0035] (In formula (A13), R 11 is -O-(CH2) n R is a divalent group represented by -O- (n is a number of 2 or more and 10 or less). 12 , R 14 , R 22 and R 24 is an electron-donating group, and R 15 and R 25 is a hydrogen atom. R 13 , R 16 , R 23 and R 26 are each independently a hydrogen atom, an alkyl group, or an electron-donating group.

[0036] (A2) One or more couplers other than the component (A1), selected from the group consisting of couplers (A2-1) having a benzene ring, electron-donating groups at the 1st and 2nd positions on the benzene ring, and hydrogen atoms at two or more of the 3rd to 6th positions, and couplers (A2-2) having a pyridine ring, electron-donating groups at the 2nd and 3rd positions on the pyridine ring, and hydrogen atoms at two or more of the 4th to 6th positions.

[0037] In this specification, the term "coupler" does not include compounds having a catechin structure. The "catechin structure" used here specifically refers to a structure represented by the following general formula (I):

[0038] [ka]

[0039] (In the formula, R A and R B are each independently a hydrogen atom or a hydroxy group. C is a hydrogen atom or an acyl group, and R D is a hydrogen atom or a ring-containing group. R C The acyl group in the formula (II) is preferably a group represented by the following formula (II), and R D The ring structure-containing group in the formula (III) is preferably a group represented by the following formula (III).

[0040] [ka]

[0041] [ka]

[0042] (In the above formula, * indicates a bond. R A ~R C is the same as above.)

[0043] [Component (A1)] Component (A1) is one or more selected from the group consisting of couplers (A1-1) having a benzene ring, electron-donating groups at the 1- and 3-positions on the benzene ring, and hydrogen atoms at the 4- and 6-positions, couplers (A1-2) having a pyridine ring, electron-donating groups at the 2- and 6-positions on the pyridine ring, and hydrogen atoms at the 3- and 5-positions, and couplers (A1-3) represented by the following general formula (A13): Couplers (A1-1) to (A1-3) may be in the form of a salt, and the type of salt is not particularly limited.

[0044] [ka]

[0045] (In formula (A13), R11 is -O-(CH2) n R is a divalent group represented by -O- (n is a number of 2 or more and 10 or less). 12 , R 14 , R 22 and R 24 is an electron-donating group, and R 15 and R 25 is a hydrogen atom. R 13 , R 16 , R 23 and R 26 are each independently a hydrogen atom, an alkyl group, or an electron-donating group.

[0046] Examples of the electron-donating group in component (A1) include a hydroxy group, a hydroxyalkyl group, an alkoxy group, a hydroxyalkoxy group, a primary to tertiary amino group, an alkylamino group, and an aromatic hydrocarbon ring structure.

[0047] <Coupler (A1-1)> The coupler (A1-1) preferably includes a compound represented by the following general formula (A11) or a salt thereof.

[0048] [ka] (In formula (A11), R 1 is an electron donating group attached to the carbon atom at position 1, R 2 is a hydrogen atom, alkyl group or electron donating group bonded to the carbon atom at the 2nd position, R 3 is an electron donating group attached to the 3-carbon atom, R 4 is a hydrogen atom, an alkyl group, or an electron-donating group bonded to the carbon atom at the 5-position. 2 and R 3 may be bonded to each other to form a hydrocarbon ring structure having aromaticity.

[0049] The electron-donating group in general formula (A11) preferably includes at least one selected from the group consisting of a hydroxy group, a hydroxyalkyl group, an alkoxy group, a hydroxyalkoxy group, a primary to tertiary amino group, an alkylamino group, and a hydrocarbon ring structure having aromaticity, more preferably includes at least one selected from the group consisting of a hydroxy group, a hydroxyalkyl group having from 2 to 8 carbon atoms, an alkoxy group having from 1 to 8 carbon atoms, a hydroxyalkoxy group having from 2 to 8 carbon atoms, a primary amino group (-NH2), and an alkylamino group having from 1 to 8 carbon atoms, and even more preferably includes at least one selected from the group consisting of a hydroxy group and a primary amino group (-NH2). The alkyl group preferably includes an alkyl group having 1 to 8 carbon atoms, more preferably an alkyl group having 1 to 3 carbon atoms, and even more preferably a methyl group. The aromatic hydrocarbon ring structure is represented by R 2 and R 3 are bonded to each other to form an aromatic hydrocarbon ring structure, the ring structure preferably includes an aromatic hydrocarbon ring structure having 5 to 8 ring carbon atoms, more preferably includes an aromatic hydrocarbon ring structure having 5 to 6 ring carbon atoms, and even more preferably includes an aromatic hydrocarbon ring structure having 6 ring carbon atoms.

[0050] In the general formula (A11), R 1 is preferably a hydroxy group or a primary amino group (-NH). 2 is preferably a hydrogen atom or a methyl group, R 3 is preferably a hydroxy group or a primary amino group (-NH). 2 and R 3 are bonded to each other to form an aromatic hydrocarbon ring structure with 6 ring carbon atoms. 4 is preferably a hydrogen atom or a methyl group, more preferably a hydrogen atom.

[0051] Specific examples of the compound represented by the general formula (A11) include one or more compounds selected from the group consisting of meta-aminophenol, resorcinol, meta-phenylenediamine, 2-methylresorcinol, 1-naphthol, and salts thereof, and preferably include one or more compounds selected from the group consisting of meta-aminophenol, resorcinol, 2-methylresorcinol, 1-naphthol, and salts thereof.

[0052] <Coupler (A1-2)> The coupler (A1-2) preferably includes a compound represented by the following general formula (A12) or a salt thereof.

[0053] [ka]

[0054] (In formula (A12), R 5 is an electron donating group attached to the 2nd carbon atom, R 6 represents a hydrogen atom, an alkyl group, or an electron-donating group bonded to the 4-carbon atom; R 7 is an electron-donating group attached to the 6-carbon atom.)

[0055] The electron-donating group in general formula (A12) preferably includes one or more selected from the group consisting of a hydroxy group, a hydroxyalkyl group, an alkoxy group, a hydroxyalkoxy group, a primary to tertiary amino group, and an alkylamino group, more preferably includes one or more selected from the group consisting of a hydroxy group, a hydroxyalkyl group having from 2 to 8 carbon atoms, an alkoxy group having from 1 to 8 carbon atoms, a hydroxyalkoxy group having from 2 to 8 carbon atoms, a primary amino group (-NH2), and an alkylamino group having from 1 to 8 carbon atoms, and even more preferably includes one or more selected from the group consisting of a hydroxy group and a primary amino group (-NH2). The alkyl group preferably includes an alkyl group having 1 to 8 carbon atoms, more preferably an alkyl group having 1 to 3 carbon atoms, and even more preferably a methyl group.

[0056] In the general formula (A12), R 5is preferably a hydroxy group or a primary amino group (—NH), and R 6 is preferably a hydrogen atom or a methyl group. 7 is preferably a primary amino group (-NH2). Specific examples of the compound represented by the general formula (A12) include 2,6-diaminopyridine and salts thereof.

[0057] <Coupler (A1-3)> The coupler (A1-3) preferably includes a compound represented by the following general formula (A13) or a salt thereof.

[0058] [ka]

[0059] (In formula (A13), R 11 is -O-(CH2) n R is a divalent group represented by -O- (n is a number of 2 or more and 10 or less). 12 , R 14 , R 22 and R 24 is an electron-donating group, and R 15 and R 25 is a hydrogen atom. R 13 , R 16 , R 23 and R 26 are each independently a hydrogen atom, an alkyl group, or an electron-donating group. The electron-donating group, the alkyl group, and preferred embodiments thereof in formula (A13) are the same as those in formula (A12).

[0060] In general formula (A13), R 11 In the formula, n is preferably 2 or more and 8 or less, and more preferably 2 or more and 4 or less. R 12 , R 14 , R 22 and R 24 The electron donating group in R preferably comprises a hydroxy group or a primary amino group (-NH), more preferably a primary amino group (-NH).13 , R 16 , R 23 and R 26 preferably contains a hydrogen atom or a methyl group, and more preferably is a hydrogen atom. Specific examples of the coupler represented by the general formula (A13) include 1,3-bis(2,4-diaminophenoxy)propane and salts thereof.

[0061] As the component (A1), one or more members selected from the group consisting of the couplers (A1-1), (A1-2), and (A1-3) can be used. Among the above, component (A1) preferably contains one or more compounds selected from the group consisting of compounds represented by general formula (A11), compounds represented by general formula (A12), compounds represented by general formula (A13), and salts thereof, more preferably contains one or more compounds selected from the group consisting of meta-aminophenol, resorcinol, meta-phenylenediamine, 2-methylresorcinol, 1-naphthol, 2,6-diaminopyridine, 1,3-bis(2,4-diaminophenoxy)propane, and salts thereof, and even more preferably contains one or more compounds selected from the group consisting of meta-aminophenol, resorcinol, 2-methylresorcinol, 1-naphthol, and salts thereof.

[0062] [Ingredient (A2)] Component (A2) is a coupler other than component (A1), and is at least one selected from the group consisting of couplers (A2-1) having a benzene ring, electron-donating groups at the 1- and 2-positions on the benzene ring, and hydrogen atoms at two or more of the 3- to 6-positions, and couplers (A2-2) having a pyridine ring, electron-donating groups at the 2- and 3-positions on the pyridine ring, and hydrogen atoms at two or more of the 4- to 6-positions.

[0063] 《Coupler (A2-1)》 The coupler (A2-1) preferably includes a compound represented by the following general formula (A21) or a salt thereof, excluding couplers corresponding to the above component (A1).

[0064] [ka]

[0065] (In formula (A21), R 31 is an electron donating group attached to the carbon atom at position 1, R 32 is an electron donating group attached to the 2nd carbon atom, R 33 ~R 36 are hydrogen atoms, alkyl groups, or electron-donating groups bonded to the 3-, 4-, 5-, and 6-position carbons, respectively. 33 ~R 36 At least two of these are hydrogen atoms.)

[0066] The electron-donating group in general formula (A21) preferably includes one or more selected from the group consisting of a hydroxy group, a hydroxyalkyl group, an alkoxy group, a hydroxyalkoxy group, a primary to tertiary amino group, and an alkylamino group, more preferably includes one or more selected from the group consisting of a hydroxy group, a hydroxyalkyl group having from 2 to 8 carbon atoms, an alkoxy group having from 1 to 8 carbon atoms, a hydroxyalkoxy group having from 2 to 8 carbon atoms, a primary amino group (-NH2), and an alkylamino group having from 1 to 8 carbon atoms, and even more preferably includes one or more selected from the group consisting of a hydroxy group, a hydroxyalkoxy group having from 2 to 8 carbon atoms, and a primary amino group (-NH2). The alkyl group preferably includes an alkyl group having 1 to 8 carbon atoms, more preferably includes an alkyl group having 1 to 3 carbon atoms, and further preferably includes a methyl group.

[0067] In general formula (A21), R 31 is preferably a hydroxy group, a hydroxyalkoxy group having from 2 to 8 carbon atoms, or a primary amino group (-NH), and more preferably a hydroxy group, a hydroxyethoxy group, or a primary amino group (-NH). 32 is preferably a hydroxy group or a primary amino group (-NH2), more preferably a primary amino group (-NH2).

[0068] Specific examples of the compound represented by general formula (A21) include ortho-aminophenol, 2,4-diaminophenoxyethanol, and salts thereof.

[0069] 《Coupler (A2-2)》 The coupler (A2-2) preferably includes a compound represented by the following general formula (A22) or a salt thereof.

[0070] [ka]

[0071] (In formula (A22), R 37 is an electron donating group attached to the 2nd carbon atom, R 38 is an electron donating group attached to the 3-carbon atom. 39 ~R 41 are hydrogen atoms, alkyl groups, or electron-donating groups bonded to the 4-, 5-, and 6-position carbons, respectively. 39 ~R 41 At least two of these are hydrogen atoms.)

[0072] The electron-donating group, the alkyl group, and preferred embodiments thereof in formula (A22) are the same as those in formula (A21).

[0073] In the general formula (A22), R 37 is preferably a hydroxy group or a primary amino group (—NH), and R 38 is preferably a hydroxy group or a primary amino group (-NH), more preferably a primary amino group (-NH). 39 ~R 41 are each independently preferably a hydrogen atom or a methyl group, more preferably R 39 ~R 41 All of these are hydrogen atoms. Specific examples of the compound represented by the general formula (A22) include 2,3-diaminopyridine, 2-amino-3-hydroxypyridine, and salts thereof.

[0074] As the component (A2), one or more members selected from the group consisting of the above couplers (A2-1) and (A2-2) can be used. Among the above, component (A2) preferably contains a coupler (A2-1), and more preferably contains one or more selected from the group consisting of ortho-aminophenol, 2,4-diaminophenoxyethanol, and salts thereof.

[0075] Among the above, from the viewpoint of compatibility, the oxidation dye intermediate (A) preferably contains component (A1), and more preferably contains one or more selected from the group consisting of meta-aminophenol, resorcinol, meta-phenylenediamine, 2-methylresorcinol, 1-naphthol, 2,6-diaminopyridine, 1,3-bis(2,4-diaminophenoxy)propane, and salts thereof. The oxidation dye intermediate (A) preferably contains a coupler (A1-1), more preferably one or more selected from the group consisting of meta-aminophenol, resorcinol, 2-methylresorcinol, and 1-naphthol.

[0076] From the viewpoint of improving dyeability and fastness, the total content of components (A1) and (A2) in the oxidation dye intermediate (A) is preferably 30% by mass or more, more preferably 40% by mass or more, and 100% by mass or less. Furthermore, when the oxidation dye intermediate (A) contains another oxidation dye intermediate (for example, a precursor of component (A3) described below), the total content of components (A1) and (A2) in the oxidation dye intermediate (A) may be, for example, 90% by mass or less, 80% by mass or less, 70% by mass or less, or 60% by mass or less.

[0077] From the viewpoint of improving dyeability and fastness, the content of component (A1) in the oxidation dye intermediate (A) is preferably 30% by mass or more, more preferably 40% by mass or more, and 100% by mass or less. The content of component (A1) in the oxidation dye intermediate (A) may be, for example, 90% by mass or less, 80% by mass or less, 70% by mass or less, or 60% by mass or less.

[0078] (Component (A3): Precursor) From the viewpoint of further improving dyeability and fastness, the oxidation dye intermediate (A) preferably further contains component (A3): precursor as an oxidation dye intermediate other than the components (A1) and (A2). The precursor can be any compound known as a precursor of an oxidation dye intermediate, without any limitation, and examples thereof include paraphenylenediamine, toluene-2,5-diamine, orthochloroparaphenylenediamine, N-phenylparaphenylenediamine, N,N-bis(hydroxyethyl)paraphenylenediamine, 3-methyl-4-aminophenol, 2-hydroxyethylparaphenylenediamine, paraaminophenol, paramethylaminophenol, 4-amino-metacresol, and salts thereof.

[0079] Among the above, from the viewpoint of further improving fastness when used in combination with the couplers of components (A1) and (A2), component (A3) preferably includes one or more members selected from the group consisting of toluene-2,5-diamine, para-aminophenol, 4-amino-metacresol, 1-hydroxyethyl-4,5-diaminopyrazole, and salts thereof.

[0080] When the oxidation dye intermediate (A) contains component (A3), the content of component (A3) in the oxidation dye intermediate (A) is preferably 20% by mass or more, more preferably 30% by mass or more, even more preferably 40% by mass or more, and is preferably 70% by mass or less, more preferably 65% ​​by mass or less, and even more preferably 60% by mass or less, from the viewpoint of further improving dyeability and fastness. When the oxidation dye intermediate (A) contains component (A3), the content of component (A3) in the oxidation dye intermediate (A) is preferably 20% by mass or more and 70% by mass or less, more preferably 30% by mass or more and 65% by mass or less, and even more preferably 40% by mass or more and 60% by mass or less.

[0081] The oxidation dye intermediate (A) may further contain a coupler other than the components (A1) and (A2). However, from the viewpoint of further improving dyeability and fastness, the total content of the components (A1) to (A3) in the oxidation dye intermediate (A) is preferably 70% by mass or more, more preferably 80% by mass or more, even more preferably 90% by mass or more, still more preferably 95% by mass or more, and even more preferably 98% by mass or more, but not more than 100% by mass. That is, the content of couplers other than the components (A1) and (A2) in the oxidation dye intermediate (A) is preferably 30% by mass or less, more preferably 20% by mass or less, even more preferably 10% by mass or less, still more preferably 5% by mass or less, and even more preferably 2% by mass or less, and may be 0% by mass.

[0082] From the viewpoint of further improving dyeability and fastness, the molecular weight of the oxidation dye intermediate (A) is, as a non-dissociated type, preferably 95 or more, more preferably 100 or more, and even more preferably 105 or more, and from the viewpoint of efficiently penetrating into the interior of the fiber to further improve dyeability, the molecular weight of the oxidation dye intermediate (A) is, as a non-dissociated type, preferably 500 or less, more preferably 300 or less, and even more preferably 200 or less. The molecular weight of the oxidation dye intermediate (A) is, as a non-dissociated type, preferably 95 or more and 500 or less, more preferably 100 or more and 300 or less, and even more preferably 105 or more and 200 or less. The molecular weight of the oxidative dye intermediate (A) refers to the molecular weight of each oxidative dye intermediate in the oxidative dye intermediate (A), and it is preferable that the undissociated molecular weights of the components (A1), (A2), and (A3) are all within the above range. Furthermore, the undissociated molecular weight of the oxidative dye intermediate (A) refers to the molecular weight of the oxidative dye intermediate (A) in a non-ionic state, even when the oxidative dye intermediate (A) is a salt, and does not include the molecular weight of the counter ion. This also includes cases where the oxidative dye intermediate (A) has an onium group such as a quaternary ammonium group, and in such cases, the counter ion is similarly not included in the molecular weight.

[0083] (Alkaline agent) The alkaline agent used in the first agent may be either an inorganic alkaline agent or an organic alkaline agent. Examples of the alkaline agent include ammonia; alkanolamines such as mono-, di-, or trimethanolamine, and mono-, di-, or triethanolamine; alkylamines such as methylamine, dimethylamine, ethylamine, diethylamine, N-methylethylamine, propylamine, and butylamine; aralkylamines such as benzylamine; and inorganic alkali compounds such as sodium hydroxide and potassium hydroxide, and one or more of these can be used. From the viewpoint of water solubility, the number of carbon atoms in the alkanolamine, alkylamine, or aralkylamine is preferably 10 or less, and more preferably 8 or less. Among the above, from the viewpoint of efficiently penetrating the oxidation dye intermediate (A) into the interior of the fiber to further improve dyeability and fastness, the alkaline agent preferably contains one or more selected from the group consisting of ammonia, alkanolamine, alkylamine, aralkylamine, sodium hydroxide, and potassium hydroxide, and more preferably contains one or more selected from the group consisting of ammonia and alkanolamine.

[0084] (water) The water used in the first agent is not particularly limited, and for example, ion-exchanged water, pure water, distilled water, etc. can be used.

[0085] (Other ingredients) In addition to the above ingredients, the first agent may contain antioxidants, fragrances, preservatives, thickeners, pH adjusters, surfactants, texture improvers, and the like.

[0086] (Content) The content of each component in the first agent is preferably within the following ranges. From the viewpoint of improving dyeability, the content of component (A) in the first pack is preferably 0.01% by mass or more, more preferably 0.02% by mass or more, even more preferably 0.05% by mass or more, still more preferably 0.1% by mass or more, still more preferably 0.2% by mass or more, still more preferably 0.3% by mass or more, and still more preferably 0.5% by mass or more, and from the viewpoint of improving formulation stability, it is preferably 5.0% by mass or less, more preferably 3.0% by mass or less, and still more preferably 2.0% by mass or less. The content of component (A) in the first pack is preferably 0.01% by mass or more and 5.0% by mass or less, more preferably 0.02% by mass or more and 3.0% by mass or less, still more preferably 0.05% by mass or more and 3.0% by mass or less, still more preferably 0.1% by mass or more and 3.0% by mass or less, still more preferably 0.2% by mass or more and 3.0% by mass or less, still more preferably 0.3% by mass or more and 3.0% by mass or less, and still more preferably 0.5% by mass or more and 2.0% by mass or less.

[0087] From the viewpoint of improving dyeability, the total content of component (A1) and component (A2) in the first agent is preferably 0.01% by mass or more, more preferably 0.02% by mass or more, even more preferably 0.05% by mass or more, still more preferably 0.1% by mass or more, still more preferably 0.2% by mass or more, and still more preferably 0.25% by mass or more, and from the viewpoint of improving formulation stability, it is preferably 5.0% by mass or less, more preferably 3.0% by mass or less, even more preferably 2.0% by mass or less, still more preferably 1.5% by mass or less, and still more preferably 1.0% by mass or less. The total content of component (A1) and component (A2) in the first agent is preferably 0.01% by mass or more and 5.0% by mass or less, more preferably 0.02% by mass or more and 3.0% by mass or less, even more preferably 0.05% by mass or more and 2.0% by mass or less, still more preferably 0.1% by mass or more and 1.5% by mass or less, still more preferably 0.2% by mass or more and 1.5% by mass or less, and still more preferably 0.25% by mass or more and 1.0% by mass or less.

[0088] From the viewpoint of improving dyeability and fastness, the content of the alkaline agent in the first agent is preferably 0.01% by mass or more, more preferably 0.1% by mass or more, even more preferably 0.5% by mass or more, and even more preferably 1.0% by mass or more. From the viewpoint of maintaining constant reactivity, it is preferably 10% by mass or less, more preferably 7.5% by mass or less, and even more preferably 5.0% by mass or less. The content of the alkaline agent in the first agent is preferably 0.01% by mass or more and 10% by mass or less, more preferably 0.1% by mass or more and 7.5% by mass or less, even more preferably 0.5% by mass or more and 7.5% by mass or less, and even more preferably 1.0% by mass or more and 5.0% by mass or less. The content of the alkaline agent herein means an effective amount of the alkaline agent.

[0089] The content of water in the first agent is preferably 70% by mass or more, more preferably 80% by mass or more, even more preferably 85% by mass or more, and preferably 99.98% by mass or less, from the viewpoint of improving the solubility of the oxidation dye intermediate (A) and the alkaline agent, and from the viewpoint of improving the ease of handling when mixed with the second agent. The content of water in the first agent may be the balance of the oxidation dye intermediate (A) and the alkaline agent.

[0090] (pH) From the viewpoint of improving dyeability and fastness, the pH of the first agent is preferably 6 or higher, more preferably 8 or higher, and even more preferably 10 or higher. From the viewpoint of maintaining constant reactivity, the pH is preferably 12.0 or lower, more preferably 11.5 or lower, and even more preferably 11.0 or lower. The pH of the first agent is preferably 6 or higher and 12.0 or lower, more preferably 8 or higher and 11.5 or lower, and even more preferably 10 or higher and 11.0 or lower. The pH can be measured at 25°C by the method described in the Examples.

[0091] (Dosage form, manufacturing method) The dosage form of the first agent is not particularly limited, and can be liquid, paste, cream, gel, foam, spray, wax, or other dosage form depending on the product form, with liquid being preferred. The method for producing the first agent is not particularly limited, and it can be produced by mixing the components by any method. The first agent of this embodiment can be preferably obtained by mixing a medium (e.g., water) with the dye and other components under heating (e.g., 60 to 80°C) to uniformly dissolve or disperse the dye and other components, and then adding an alkaline agent at room temperature and mixing uniformly.

[0092] <Second agent> The second agent contains hydrogen peroxide and water. From the viewpoint of improving dyeability and fastness, the content of hydrogen peroxide in the second agent is preferably 0.1% by mass or more, more preferably 0.5% by mass or more, and even more preferably 1.0% by mass or more, and from the viewpoint of suppressing damage to the fibers, it is preferably 10% by mass or less, more preferably 8.0% by mass or less. The content of hydrogen peroxide in the second agent is preferably 0.1% by mass or more and 10% by mass or less, more preferably 0.5% by mass or more and 10% by mass or less, and even more preferably 1.0% by mass or more and 8.0% by mass or less. From the viewpoint of ease of handling, hydrogen peroxide is preferably blended in the form of an aqueous solution. In this specification, the content of hydrogen peroxide in the second agent means an effective amount of hydrogen peroxide.

[0093] (water) The water used in the second agent is not particularly limited, and for example, ion-exchanged water, pure water, distilled water, etc. can be used. From the viewpoint of improving the ease of handling when mixed with the first agent, the water content in the second agent is preferably 70% by mass or more, more preferably 80% by mass or more, even more preferably 85% by mass or more, and is preferably 99.9% by mass or less. The content of water in the second agent comprises the remainder of the hydrogen peroxide.

[0094] (Other ingredients) In addition to the above ingredients, the second agent may contain antioxidants, fragrances, preservatives, thickeners, pH adjusters, surfactants, texture improvers, and the like.

[0095] (pH) The pH of the second agent is preferably 2.5 or higher, more preferably 3.0 or higher, and is preferably 6 or lower, more preferably 5 or lower, and even more preferably 4 or lower. The pH of the second agent is preferably 2.5 or higher and 6 or lower, more preferably 2.5 or higher and 5 or lower, and even more preferably 3.0 or higher and 4 or lower. The pH can be measured at 25°C by the method described in the Examples.

[0096] (Dosage form, manufacturing method) The dosage form of the second agent is not particularly limited, and can be liquid, paste, cream, gel, foam, spray, wax, or other dosage form depending on the product form, with liquid being preferred. The first and second agents may be in the same or different dosage forms, but from the viewpoint of ease of handling during use, it is preferable that they be in the same dosage form. The method for producing the second agent is not particularly limited, and examples include a method of mixing the components by any method. The second agent of this embodiment can be preferably obtained by mixing a medium (e.g., water) and other components under heating (e.g., 60 to 80°C) to dissolve them uniformly, and then adding hydrogen peroxide at room temperature and mixing them uniformly.

[0097] The composition of the present invention is used by mixing at least the first agent and the second agent. The mixing may be carried out at the time of use, or a mixture that has been mixed in advance may be used, but it is preferable to mix them at the time of use. Note that the composition of the present invention may be used by mixing at least the first agent and the second agent, and may further include, for example, a third agent or more containing other components. The mixing ratio of the first agent to the second agent varies depending on the concentrations of the oxidative dye intermediate (A) and alkaline agent in the first agent and the hydrogen peroxide in the second agent, but the first agent:second agent (mass ratio) is preferably in the range of 1:0.1 to 1:10, more preferably 1:0.2 to 1:5, and even more preferably 1:0.5 to 1:3. After mixing the first and second agents, the pH may be further adjusted before use. The pH at 25°C is preferably 3.0 or higher, more preferably 3.5 or higher, and even more preferably 4.0 or higher. From the viewpoint of suppressing damage to fibers, the pH is preferably 7.5 or lower, more preferably 7.0 or lower, and even more preferably 6.5 or lower. The pH of the composition after mixing the first and second agents is preferably 3.0 or higher and 7.5 or lower, more preferably 3.5 or higher and 7.0 or lower, and even more preferably 4.0 or higher and 6.5 or lower, at 25°C.

[0098] Furthermore, the mass ratio [{(A1) + (A2)} / hydrogen peroxide] of the total content of the oxidative dye intermediates (Components (A1) and (A2)) in the first agent to the hydrogen peroxide in the second agent is preferably 0.001 or more, more preferably 0.005 or more, even more preferably 0.01 or more, and even more preferably 0.03 or more, from the viewpoint of suppressing damage to fibers caused by hydrogen peroxide. Furthermore, from the viewpoint of improving dyeability and fastness, it is preferably 50 or less, more preferably 20 or less, even more preferably 5 or less, even more preferably 1.0 or less, and even more preferably 0.5 or less. That is, the mass ratio [{(A1) + (A2)} / hydrogen peroxide] is preferably 0.001 or more and 50 or less, more preferably 0.005 or more and 20 or less, even more preferably 0.01 or more and 5 or less, even more preferably 0.03 or more and 1.0 or less, and even more preferably 0.03 or more and 0.5 or less. The mass of hydrogen peroxide refers to the amount of active ingredient.

[0099] (Content) The content of each component in the dye composition for regenerated collagen fibers obtained by mixing at least the first agent and the second agent is preferably within the following range. From the viewpoint of improving dyeability, the content of component (A) or a reaction product of component (A) in the composition is preferably 0.005% by mass or more, more preferably 0.01% by mass or more, even more preferably 0.02% by mass or more, still more preferably 0.03% by mass or more, still more preferably 0.05% by mass or more, still more preferably 0.1% by mass or more, and still more preferably 0.2% by mass or more, and from the viewpoint of improving formulation stability, it is preferably 3.0% by mass or less, more preferably 2.0% by mass or less, and even more preferably 1.0% by mass or less. The content of component (A) or a reaction product of component (A) in the composition is preferably 0.005% by mass or more and 3.0% by mass or less, more preferably 0.01% by mass or more and 3.0% by mass or less, even more preferably 0.02% by mass or more and 3.0% by mass or less, still more preferably 0.03% by mass or more and 2.0% by mass or less, even more preferably 0.05% by mass or more and 2.0% by mass or less, still more preferably 0.1% by mass or more and 2.0% by mass or less, and still more preferably 0.2% by mass or more and 1.0% by mass or less.

[0100] From the viewpoint of improving dyeability and fastness, the content of the alkaline agent in the composition is preferably 0.005% by mass or more, more preferably 0.01% by mass or more, even more preferably 0.1% by mass or more, still more preferably 0.5% by mass or more, and even more preferably 1.0% by mass or more. Furthermore, from the viewpoint of maintaining constant reactivity, the content is preferably 5.0% by mass or less, more preferably 3.5% by mass or less, and even more preferably 2.5% by mass or less. The content of the alkaline agent in the composition is preferably 0.005% by mass or more and 5.0% by mass or less, more preferably 0.01% by mass or more and 3.5% by mass or less, even more preferably 0.1% by mass or more and 3.5% by mass or less, still more preferably 0.5% by mass or more and 3.5% by mass or less, and even more preferably 1.0% by mass or more and 2.5% by mass or less.

[0101] From the viewpoint of suppressing damage to fibers, the content of hydrogen peroxide in the composition is preferably 5.0% by mass or less, more preferably 4.0% by mass or less, even more preferably 3.5% by mass or less, still more preferably 2.5% by mass or less, still more preferably 1.0% by mass or less, still more preferably 0.1% by mass or less, still more preferably 0.01% by mass or less, and still more preferably none.

[0102] The water content in the composition is preferably 70% by mass or more, more preferably 80% by mass or more, even more preferably 85% by mass or more, and preferably 99.9% by mass or less.

[0103] <Modified regenerated collagen fiber> The regenerated collagen fibers to be dyed with the dye composition of the present invention include modified regenerated collagen fibers containing one or more compounds (B) selected from the group consisting of the following components (B1) and (B2): (B1) Benzoic acid or its salts (B2) A copolymer containing a structural unit derived from an unsaturated monomer having a carboxy group and a structural unit derived from an aromatic vinyl compound, the copolymer having an acid value of 100 mgKOH / g or more and a weight average molecular weight of 1500 or more and 15000 or less, or a salt thereof.

[0104] (Compound (B)) Compound (B) is one or more compounds selected from the group consisting of component (B1) and component (B2), and is a modifier for regenerated collagen fibers. The regenerated collagen fibers to be modified by compound (B) will be described later.

[0105] [Component (B1)] Component (B1) is benzoic acid or a salt thereof. When component (B1) is a salt, examples thereof include alkali metal salts such as sodium salts and potassium salts. Specific examples of component (B1) include one or more selected from the group consisting of benzoic acid, sodium benzoate, and potassium benzoate, and preferably include one or more selected from the group consisting of benzoic acid and sodium benzoate.

[0106] [Component (B2)] Component (B2) is a copolymer containing structural units derived from an unsaturated monomer having a carboxy group and structural units derived from an aromatic vinyl compound, and is a copolymer or a salt thereof having an acid value of 100 mgKOH / g or more and a weight average molecular weight of 1,500 or more and 15,000 or less.

[0107] In component (B2), the structural unit derived from an unsaturated monomer having a carboxy group may be derived from an unsaturated monocarboxylic acid, an unsaturated dicarboxylic acid, or a combination thereof. Specific examples of the unsaturated monomer having a carboxy group include unsaturated monocarboxylic acids and unsaturated dicarboxylic acids. Examples of unsaturated monocarboxylic acids include acrylic acid, methacrylic acid, crotonic acid, oleic acid, and cyclopentenylacetic acid, and examples of unsaturated dicarboxylic acids include maleic acid, fumaric acid, citraconic acid, mesaconic acid, itaconic acid, and methylene succinic acid. Alternatively, an unsaturated dicarboxylic acid anhydride may be used as the unsaturated monomer having a carboxy group, and may be converted into an acid form by hydrolysis with an alkali, etc. Examples of unsaturated dicarboxylic acid anhydrides include maleic anhydride and citraconic anhydride. The unsaturated monomers having a carboxy group can be used alone or in combination of two or more kinds.

[0108] The structural unit derived from an aromatic vinyl compound in component (B2) is not particularly limited as long as it is derived from an aromatic compound substituted with at least a vinyl group. Specific examples of aromatic vinyl compounds include styrene, α-methylstyrene, p-methylstyrene, 3-vinyltoluene, dimethylstyrene, ethylvinylbenzene, chloromethylstyrene, vinylnaphthalene, and vinylanthracene. The aromatic vinyl compounds can be used alone or in combination of two or more kinds.

[0109] In component (B2), the bonding state of the monomers that give rise to each structural unit may be block bonding, random bonding, or a combination thereof.

[0110] Component (B2) may contain structural units other than the above unsaturated monomers. Examples of other structural units include, but are not limited to, structural units derived from unsaturated aliphatic hydrocarbon compounds, such as linear, branched, or cyclic unsaturated aliphatic hydrocarbon compounds. Examples of the linear or branched unsaturated aliphatic hydrocarbon compound include propylene, isobutylene, diisobutylene, triisobutylene, tripropylene, and tetrapropylene. Examples of the cyclic unsaturated aliphatic hydrocarbon compound include cyclopentene, cyclohexene, and cyclooctene. The structural units derived from the unsaturated aliphatic hydrocarbon compound may include one or more types.

[0111] A suitable embodiment of component (B2) is, for example, a copolymer containing structural units derived from one or more selected from the group consisting of unsaturated monocarboxylic acids and unsaturated dicarboxylic acids, and structural units derived from an aromatic vinyl compound. Specific examples of the component (B2), from the viewpoint of further improving dyeability and fastness when dyeing with the dye composition of the present invention, preferably include one or more selected from the group consisting of styrene-maleic acid copolymer, styrene-acrylic acid copolymer, styrene-methacrylic acid copolymer, vinylbenzoic acid-maleic acid copolymer, vinylbenzoic acid-acrylic acid copolymer, vinylbenzoic acid-methacrylic acid copolymer, and styrene-4-vinylbenzoic acid copolymer, and more preferably include a styrene-maleic acid copolymer.

[0112] In component (B2), the molar ratio (u1 / u2) of the structural unit (u1) derived from the unsaturated monomer having a carboxy group to the structural unit (u2) derived from the aromatic vinyl compound monomer is preferably 1 / 5 to 5 / 1, more preferably 1 / 3 to 3 / 1, and even more preferably 1 / 2 to 2 / 1.

[0113] The acid value of component (B2) is 100 mgKOH / g or more, and from the viewpoint of further improving dyeability and fastness when dyed with the dye composition of the present invention, it is preferably 200 mgKOH / g or more, more preferably 300 mgKOH / g or more, even more preferably 400 mgKOH / g or more, and preferably 1000 mgKOH / g or less, more preferably 800 mgKOH / g or less, even more preferably 600 mgKOH / g or less. The acid value of component (B2) is preferably 100 mgKOH / g or more and 1000 mgKOH / g or less, more preferably 200 mgKOH / g or more and 800 mgKOH / g or less, even more preferably 200 mgKOH / g or more and 600 mgKOH / g or less, still more preferably 300 mgKOH / g or more and 600 mgKOH / g or less, still more preferably 400 mgKOH / g or more and 600 mgKOH / g or less. Here, the acid value is the number of mg of potassium hydroxide required to neutralize 1 g of sample.

[0114] Specific examples of component (B2) having an acid value within the above range include the following compounds. Styrene-maleic acid copolymer (Styrene / maleic acid (molar ratio) = 1 / 1) 475mgKOH / g Styrene-maleic acid copolymer (Styrene / maleic acid (molar ratio) = 2 / 1) 355mgKOH / g Styrene-maleic acid copolymer (Styrene / maleic acid (molar ratio) = 3 / 1) 285mgKOH / g

[0115] Component (B2) has a weight-average molecular weight of 1,500 or more and 15,000 or less, and from the viewpoint of further improving dyeability and fastness when dyed with the dye composition of the present invention, it is preferably 3,000 or more, more preferably 5,000 or more, even more preferably 6,000 or more, and preferably 10,000 or less, more preferably 9,500 or less, even more preferably 9,000 or less. The weight-average molecular weight of component (B2) is preferably 1,500 or more and 10,000 or less, more preferably 3,000 or more and 10,000 or less, even more preferably 5,000 or more and 9,500 or less, and even more preferably 6,000 or more and 9,000 or less. The weight-average molecular weight of component (B2) may also be preferably 3,000 or more and 15,000 or less, more preferably 5,000 or more and 15,000 or less, even more preferably 6,000 or more and 10,000 or less. In this specification, the term "weight average molecular weight" refers to the weight average molecular weight in terms of polystyrene measured by gel permeation chromatography (GPC), and specifically can be measured by the method described in the examples.

[0116] The compound (B) can be used alone or in combination of two or more. Among the above, from the viewpoint of further improving dyeability and fastness when dyeing with the dye composition of the present invention, the compound (B) preferably contains one or more selected from the group consisting of benzoic acid, sodium benzoate, and a styrene-maleic acid copolymer, and more preferably contains a styrene-maleic acid copolymer.

[0117] (Content of Compound (B)) From the viewpoint of further improving dyeability and fastness when dyed using the dye composition of the present invention, the content of compound (B) in the modified regenerated collagen fiber is preferably 0.1% by mass or more, more preferably 0.5% by mass or more, even more preferably 1.0% by mass or more, even more preferably 3.0% by mass or more, even more preferably 5.0% by mass or more, even more preferably 10% by mass or more, even more preferably 15% by mass or more, even more preferably 20% by mass or more, and is preferably 70% by mass or less, more preferably 65% ​​by mass or less, even more preferably 60% by mass or less, even more preferably 55% by mass or less, even more preferably 50% by mass or less, even more preferably 45% by mass or less, and even more preferably 40% by mass or less. The content of compound (B) in the modified regenerated collagen fiber is preferably 0.1% by mass or more and 70% by mass or less, more preferably 0.5% by mass or more and 65% by mass or less, even more preferably 1.0% by mass or more and 60% by mass or less, even more preferably 3.0% by mass or more and 55% by mass or less, even more preferably 5.0% by mass or more and 50% by mass or less, even more preferably 10% by mass or more and 45% by mass or less, even more preferably 15% by mass or more and 40% by mass or less, and even more preferably 20% by mass or more and 40% by mass or less.

[0118] When the modified regenerated collagen fibers contain component (B1) as compound (B), the content of component (B1) in the modified regenerated collagen fibers means the content converted into benzoic acid.

[0119] The content of component (B) in modified regenerated collagen fibers can be measured by the following method. First, an appropriate solvent that does not decompose component (B) and can dissolve the regenerated collagen fibers is selected, and the fibers are dissolved and extracted. Then, after appropriately diluting the extracted solution, the peak area of ​​a chromatogram plotted at an absorption wavelength suitable for quantifying component (B) is measured using HPLC / UV or GPC / UV, and the content of component (B) is calculated from the peak area. Specifically, the content of component (B) in modified regenerated collagen fibers can be measured by the method described in the Examples.

[0120] The dye composition of the present invention may be configured such that the mass ratio [(B) / (A)] of the compound (B) in the fiber for head accessories to the oxidation dye intermediate (A) in the dye composition is controlled. For example, the mass ratio [(B) / (A)] of the compound (B) in the fiber for head accessories to the oxidation dye intermediate (A) in the dye composition is preferably 3 or more, more preferably 5 or more, and even more preferably 10 or more, from the viewpoints of the blendability of the oxidation dye intermediate (A) and the storage stability and dye levelness of the dye composition, and from the viewpoints of dyeability and dye levelness, is preferably 4000 or less, more preferably 2000 or less, even more preferably 1000 or less, even more preferably 500 or less, even more preferably 200 or less, still more preferably 100 or less, and even more preferably 50 or less. That is, the mass ratio [(B) / (A)] is preferably 3 or more and 4000 or less, more preferably 3 or more and 2000 or less, even more preferably 3 or more and 1000 or less, even more preferably 5 or more and 500 or less, even more preferably 10 or more and 200 or less, even more preferably 20 or more and 100 or less, and even more preferably 20 or more and 50 or less.

[0121] (Component (C): Polyvalent metal, its salt, or its complex) In order to firmly coordinate the compound (B) inside the fiber and further improve dyeability and fastness when dyed with the dye composition of the present invention, the modified regenerated collagen fiber preferably further contains a polyvalent metal, a salt thereof, or a complex thereof as component (C) in addition to the compound (B). Component (C) also acts as a modifier for the regenerated collagen fiber. Examples of component (C) include one or more polyvalent metals selected from the group consisting of calcium, magnesium, strontium, barium, zinc, chromium, aluminum, titanium, zirconium, tin, lead, antimony, iron, and copper, or salts or complexes thereof, which may be used alone or in combination of two or more. Among the above, from the viewpoint of improving water resistance and further improving dyeability and fastness when dyeing with the dye composition of the present invention, component (C) preferably contains one or more polyvalent metals selected from the group consisting of aluminum, zirconium, and titanium, or a salt or complex thereof, and more preferably contains aluminum, or a salt or complex thereof.

[0122] When the modified regenerated collagen fibers contain component (C), the content of component (C) in the modified regenerated collagen fibers is, in terms of metal element content, preferably 0.1% by mass or more, more preferably 0.5% by mass or more, even more preferably 1.0% by mass or more, even more preferably 2% by mass or more, and preferably 40% by mass or less, more preferably 30% by mass or less, even more preferably 20% by mass or less, and even more preferably 10% by mass or less, from the viewpoint of improving water resistance and further improving dyeability and fastness when dyed with the dye composition of the present invention. The content of component (C) in the modified regenerated collagen fibers is, in terms of metal element content, preferably 0.1% by mass or more and 40% by mass or less, more preferably 0.5% by mass or more and 30% by mass or less, even more preferably 1.0% by mass or more and 20% by mass or less, and even more preferably 2% by mass or more and 10% by mass or less. The amount of component (C) in the modified regenerated collagen fibers is quantified, for example, as follows: The modified regenerated collagen fibers are incinerated, alkali-fused, and dissolved in acid to prepare a solution. This solution is then appropriately diluted to prepare a measurement sample, and the metal elements are quantified using an ICP atomic emission spectrometer. The amounts of the metal elements can be measured specifically by the methods described in the Examples.

[0123] In the dye composition of the present invention, the mass ratio [(C) / (A)] of the component (C) in the fiber for head accessories to the oxidation dye intermediate (A) in the dye composition may be controlled. For example, the mass ratio [(C) / (A)] of component (C) in the fiber for head accessories to the oxidation dye intermediate (A) in the dye composition is preferably 0.3 or more, more preferably 0.5 or more, even more preferably 1.0 or more, and still more preferably 2 or more, from the viewpoints of the blendability of the oxidation dye intermediate (A) and the storage stability and level dyeing ability of the dye composition, and from the viewpoints of dyeability and level dyeing ability, is preferably 500 or less, more preferably 200 or less, even more preferably 100 or less, still more preferably 50 or less, still more preferably 20 or less, and still more preferably 10 or less. That is, the mass ratio [(C) / (A)] is preferably 0.3 or more and 500 or less, more preferably 0.3 or more and 200 or less, even more preferably 0.5 or more and 200 or less, still more preferably 0.5 or more and 100 or less, still more preferably 1.0 or more and 50 or less, still more preferably 2 or more and 20 or less, and still more preferably 2 or more and 10 or less.

[0124] (Method for manufacturing modified regenerated collagen fiber) The regenerated collagen fibers that are the raw material for modified regenerated collagen fibers do not need to be 100% collagen, and may contain natural or synthetic polymers or additives to improve quality. Furthermore, they may be post-processed regenerated collagen fibers. The preferred form of regenerated collagen fibers is filament. Filaments are generally taken out from bobbins or boxes.

[0125] Suitable regenerated collagen fibers are artificially produced fibers made from collagen-derived polymers and oligomers. Regenerated collagen fibers are typically produced by using a solubilized collagen raw material as a spinning dope, discharging this from a spinning nozzle into a coagulation bath to form fibers, and then drying the fibrous collagen in the final step. Regenerated collagen fibers before the drying step (hereinafter also referred to as "undried regenerated collagen fibers") can be produced by conventionally known methods. For example, undried regenerated collagen fibers can be obtained by discharging an aqueous collagen solution obtained by solubilizing insoluble collagen fibers made from the split hides of livestock animals through a spinning nozzle or slit, immersing the aqueous solution in an inorganic salt solution, and then recovering the fibers without drying. This method will be specifically described below.

[0126] The preferred collagen raw material for producing regenerated collagen fibers is split skin. Split skins are obtained from fresh split skins obtained by slaughtering livestock animals such as cows, or from salted raw hides. These split skins are mostly composed of insoluble collagen fibers, but they are used after removing the fleshy part that usually adheres to them in a mesh-like form, and removing the salt used to prevent spoilage and deterioration.

[0127] These insoluble collagen fibers contain impurities such as lipids (e.g., glycerides, phospholipids, and free fatty acids), glycoproteins, and proteins other than collagen (e.g., albumin). These impurities have a significant effect on spinning stability, quality (e.g., luster and strength / elongation), odor, and other factors during fiberization. Therefore, it is preferable to remove these impurities in advance by, for example, soaking in lime to hydrolyze the fat in the insoluble collagen fibers and loosen the collagen fibers, and then subjecting them to conventional leather treatments such as acid / alkali treatment, enzyme treatment, and solvent treatment.

[0128] The insoluble collagen thus treated is then subjected to a solubilization treatment to cleave the cross-linked peptide moieties. As a method for such solubilization, a commonly used known alkali solubilization method, an enzyme solubilization method, etc., can be used. Furthermore, the alkali solubilization method and the enzyme solubilization method may be used in combination.

[0129] When the alkali solubilization method is applied, it is preferable to neutralize with an acid such as hydrochloric acid. Note that, as an improved version of the conventional alkali solubilization method, for example, the method described in JP-B-46-15033 may be used.

[0130] The enzymatic solubilization method has the advantage of being able to obtain solubilized collagen with a uniform molecular weight, and is a method that can be suitably employed in the present invention. Examples of such enzymatic solubilization methods that can be employed include those described in Japanese Patent Publication Nos. 43-25829 and 43-27513.

[0131] If the collagen that has been solubilized in this way is further subjected to operations such as pH adjustment, salting out, water washing, and solvent treatment, it is possible to obtain regenerated collagen fibers with excellent quality, and therefore it is preferable to perform these treatments.

[0132] Solubilized collagen is dissolved in an acid such as hydrochloric acid, acetic acid, or lactic acid to obtain a collagen aqueous solution having a pH of 2 to 4.5 and a collagen concentration of 1% by mass or more, preferably 2% by mass or more, and 15% by mass or less, preferably 10% by mass or less. The collagen aqueous solution may be degassed under reduced pressure while stirring, or filtered to remove water-insoluble fine particles. Furthermore, the collagen aqueous solution may contain appropriate amounts of additives, such as stabilizers and water-soluble polymers, for purposes such as improving mechanical strength, water resistance, heat resistance, gloss, spinnability, coloration prevention, and preservative properties.

[0133] The collagen aqueous solution is extruded through a spinning nozzle or a slit, for example, and immersed in an inorganic salt aqueous solution to obtain undried regenerated collagen fibers. Examples of the inorganic salt aqueous solution include aqueous solutions of water-soluble inorganic salts such as sodium sulfate, sodium chloride, and ammonium sulfate. Typically, the concentration of the inorganic salt in these inorganic salt aqueous solutions is adjusted to 10 to 40% by mass. The pH of the inorganic salt aqueous solution is preferably 2 or higher, more preferably 4 or higher, and preferably 13 or lower, more preferably 12 or lower. To adjust the pH, for example, metal salts such as sodium borate and sodium acetate, hydrochloric acid, boric acid, acetic acid, and sodium hydroxide can be used. When the pH of the inorganic salt aqueous solution is within the above range, the collagen peptide bonds are less susceptible to hydrolysis, making it easier to obtain the desired fibers. The temperature of the inorganic salt aqueous solution is not particularly limited, but is generally desirably 35°C or lower, since this prevents denaturation of soluble collagen, prevents a decrease in the strength of the spun fibers, and facilitates the production of stable threads. The lower limit of the temperature of the inorganic salt aqueous solution is not particularly limited, but can generally be adjusted appropriately depending on the solubility of the inorganic salt.

[0134] The undried regenerated collagen fibers may be pretreated (crosslinked) by immersing them in an epoxy compound or a solution thereof. The amount of the epoxy compound is preferably at least 0.1 equivalent, more preferably at least 0.5 equivalent, and even more preferably at least 1 equivalent, relative to the amount of amino groups in the regenerated collagen fibers that can react with the epoxy groups of the epoxy compound, as measured by amino acid analysis, and is preferably at most 500 equivalents, more preferably at most 100 equivalents, and even more preferably at most 50 equivalents. Having the amount of the epoxy compound within this range not only ensures a sufficient water-insolubilizing effect on the regenerated collagen fibers, but is also favorable from an industrial handleability and environmental standpoint.

[0135] The epoxy compound is used as is or dissolved in various solvents. Examples of solvents include water; alcohols such as methyl alcohol, ethyl alcohol, and isopropanol; ethers such as tetrahydrofuran and dioxane; halogenated organic solvents such as dichloromethane, chloroform, and carbon tetrachloride; and neutral organic solvents such as dimethylformamide (DMF) and dimethyl sulfoxide (DMSO). These solvents may be used alone or in combination of two or more. When water is used as the solvent, an aqueous solution of an inorganic salt such as sodium sulfate, sodium chloride, or ammonium sulfate may be used as needed. Typically, the concentration of the inorganic salt in the aqueous solution is adjusted to 10 to 40% by mass. The pH of the aqueous solution may be adjusted with, for example, a metal salt such as sodium borate or sodium acetate, or hydrochloric acid, boric acid, acetic acid, or sodium hydroxide. In this case, the pH of the aqueous solution is preferably 6 or higher, more preferably 8 or higher, from the viewpoint of not slowing down the reaction between the epoxy groups of the epoxy compound and the amino groups of collagen and ensuring sufficient insolubilization in water. Furthermore, since the pH of an aqueous solution of an inorganic salt tends to decrease over time, a buffer may be used if necessary.

[0136] The temperature during treatment of undried regenerated collagen fibers with an epoxy compound is preferably 50°C or lower, from the viewpoints of preventing denaturation of the regenerated collagen fibers, preventing a decrease in the strength of the resulting fibers, and facilitating stable production of threads.

[0137] [Treatment with a fiber treatment agent containing component (C)] Here, the modified regenerated collagen fiber used in the present invention preferably contains the above-mentioned component (C) from the viewpoint of improving water resistance, and in producing the modified regenerated collagen fiber, it is preferable to treat the undried regenerated collagen fiber obtained by the above-mentioned method by the following method. First, undried regenerated collagen fibers are immersed in a fiber treatment agent containing component (C). The fiber treatment agent containing component (C) is preferably an aqueous solution containing a polyvalent metal salt or polyvalent metal complex corresponding to component (C). The polyvalent metal salt or polyvalent metal complex preferably contains an aluminum salt or aluminum complex, more preferably contains an aluminum salt. The aluminum salt is preferably basic aluminum chloride or basic aluminum sulfate represented by the following formula: Al(OH) n Cl 3-n , or Al2(OH) 2n (SO4) 3-n [In the formula, n is 0.5 to 2.5] Specific examples of the aluminum salt include aluminum sulfate, aluminum chloride, and alum, and these can be used alone or in combination of two or more.

[0138] The content of the polyvalent metal salt and polyvalent metal complex in the fiber treatment agent is preferably 0.3 mass % or more and 5 mass % or less in terms of polyvalent metal oxide (aluminum oxide when the polyvalent metal is aluminum).

[0139] In order to prevent the polyvalent metal salt or polyvalent metal complex from being rapidly absorbed into the undried regenerated collagen fibers and causing uneven concentration, inorganic salts such as sodium chloride, sodium sulfate, and potassium chloride may be added to the fiber treatment agent as appropriate.

[0140] The pH of the fiber treatment agent at 25°C is preferably in the range of 2.5 or more and 5 or less, and can be adjusted using, for example, hydrochloric acid, sulfuric acid, acetic acid, sodium hydroxide, sodium carbonate, etc. A pH of 2.5 or more can suppress denaturation of the collagen structure, while a pH of 5 or less reduces the risk of precipitation of polyvalent metal salts or polyvalent metal complexes. It is preferable to initially adjust the pH to 2.2 or more and 3.5 or less to allow the aqueous solution of the polyvalent metal salt or polyvalent metal complex to sufficiently penetrate into the undried regenerated collagen fibers, and then add, for example, sodium hydroxide, sodium carbonate, etc. to adjust the pH to 3.5 or more and 5 or less to complete the treatment. When a highly basic polyvalent metal salt or polyvalent metal complex is used, only an initial pH adjustment of 2.5 or more and 5 or less is sufficient.

[0141] When treating with a fiber treatment agent containing component (C), the bath ratio of undried regenerated collagen fibers to the fiber treatment agent (dry mass of undried regenerated collagen fibers:mass of the fiber treatment agent) is preferably 1:2 to 1:500, more preferably 1:3 to 1:250, even more preferably 1:5 to 1:100, and even more preferably 1:20 to 1:50, when the mass of fibers after conditioning at 20°C and a relative humidity of 65% for 24 hours is taken as the dry mass.

[0142] The temperature during treatment with the fiber treatment agent containing component (C) (liquid temperature of the fiber treatment agent) is not particularly limited, but is preferably 5°C or higher, more preferably 10°C or higher, and is preferably 50°C or lower, more preferably 45°C or lower.

[0143] The treatment time (immersion time) with the fiber treatment agent containing component (C) is preferably 15 minutes or more, more preferably 30 minutes or more, even more preferably 1 hour or more, and even more preferably 3 hours or more, and is preferably 48 hours or less, more preferably 33 hours or less, and even more preferably 20 hours or less.

[0144] After treating the undried regenerated collagen fibers with an epoxy compound and / or the fiber treatment agent, the fibers may be washed with water, for example, by washing with running water for 10 minutes to 4 hours.

[0145] [Treatment with a fiber treatment agent containing component (B)] Regenerated collagen fibers, or undried regenerated collagen fibers obtained by treatment with a fiber treatment agent containing component (C), are treated with a fiber treatment agent containing component (B) to obtain modified regenerated collagen fibers that can be dyed with the dye composition of the present invention.

[0146] From the viewpoint of improving penetration into fibers and improving treatment effects, the content of component (B) in the fiber treatment agent is preferably 0.3% by mass or more, more preferably 0.5% by mass or more, even more preferably 1.0% by mass or more, still more preferably 2.5% by mass or more, still more preferably 3.0% by mass or more, and preferably 60% by mass or less, more preferably 40% by mass or less, and even more preferably 35% by mass or less. The content of component (B) in the fiber treatment agent is preferably 0.3% by mass or more and 60% by mass or less, more preferably 0.5% by mass or more and 60% by mass or less, even more preferably 1.0% by mass or more and 40% by mass or less, still more preferably 2.5% by mass or more and 40% by mass or less, and still more preferably 3.0% by mass or more and 35% by mass or less.

[0147] When component (B1) is used as component (B), the content of component (B1) in the fiber treatment agent, converted into benzoic acid, is even more preferably 5% by mass or more, even more preferably 10% by mass or more, even more preferably 15% by mass or more, even more preferably 20% by mass or more, and even more preferably 30% by mass or less, from the viewpoint of improving penetration into fibers and improving the treatment effect. When component (B1) is used as component (B), the content of component (B1) in the fiber treatment agent, calculated as benzoic acid, is preferably 0.3% by mass or more and 60% by mass or less, more preferably 0.5% by mass or more and 60% by mass or less, even more preferably 1.0% by mass or more and 40% by mass or less, still more preferably 2.5% by mass or more and 40% by mass or less, still more preferably 3.0% by mass or more and 35% by mass or less, still more preferably 5% by mass or more and 30% by mass or less, still more preferably 10% by mass or more and 30% by mass or less, still more preferably 15% by mass or more and 30% by mass or less, and still more preferably 20% by mass or more and 30% by mass or less.

[0148] When component (B2) is used as component (B), the content of component (B2) in the fiber treatment agent is more preferably 4% by mass or more, and more preferably 30% by mass or less, more preferably 20% by mass or less, more preferably 10% by mass or less, and more preferably 5% by mass or less, from the viewpoint of improving penetration into fibers and improving treatment effects. When component (B2) is used as component (B), the content of component (B2) in the fiber treatment agent is preferably 0.3% by mass to 60% by mass, more preferably 0.5% by mass to 60% by mass, even more preferably 1.0% by mass to 40% by mass, even more preferably 2.5% by mass to 40% by mass, even more preferably 3.0% by mass to 35% by mass, even more preferably 4% by mass to 30% by mass, even more preferably 4% by mass to 20% by mass, even more preferably 4.0% by mass to 10% by mass, and even more preferably 4% by mass to 5% by mass.

[0149] The fiber treating agent containing component (B) preferably further contains a pH adjuster. The pH adjuster is not particularly limited as long as it can adjust the pH to the desired level, and examples thereof include alkalis such as sodium hydroxide and potassium hydroxide, and acids such as phosphoric acid, sulfuric acid and hydrochloric acid.

[0150] The fiber treating agent containing component (B) further contains water. The water content in the fiber treating agent is preferably 40% by mass or more, more preferably 50% by mass or more, even more preferably 60% by mass or more, and even more preferably 70% by mass or more, and is preferably 99.7% by mass or less.

[0151] The pH of the fiber treatment agent containing component (B) at 25°C is preferably 3.0 or higher, more preferably 3.5 or higher, and even more preferably 4.0 or higher, from the viewpoint of suppressing damage to the fiber, and is preferably 7.5 or lower, more preferably 7.0 or lower, and even more preferably 6.5 or lower, from the viewpoint of suppressing damage to the fiber. The pH of the fiber treatment agent containing component (B) at 25°C is preferably 3.0 or higher and 7.5 or lower, more preferably 3.5 or higher and 7.0 or lower, and even more preferably 4.0 or higher and 6.5 or lower. The pH can be measured by the method described in the Examples.

[0152] Treatment with a fiber treatment agent containing component (B) can be carried out by immersing the regenerated collagen fibers, or undried regenerated collagen fibers obtained by treatment with a fiber treatment agent containing component (C), in the fiber treatment agent containing component (B).

[0153] When treating with a fiber treatment agent containing component (B), the bath ratio of regenerated collagen fibers or undried regenerated collagen fibers to the fiber treatment agent (dry mass of regenerated collagen fibers or undried regenerated collagen fibers:mass of the fiber treatment agent), when the mass of fibers after conditioning at 20°C and a relative humidity of 65% for 24 hours is taken as the dry mass, is preferably 1:2 to 1:500, more preferably 1:3 to 1:250, even more preferably 1:5 to 1:100, and even more preferably 1:20 to 1:50.

[0154] The temperature during treatment with a fiber treatment agent containing component (B) (the temperature of the fiber treatment agent) is preferably 20°C or higher, more preferably 25°C or higher, and even more preferably 30°C or higher, from the viewpoint of improving penetration into fibers, and from the viewpoint of suppressing damage to fibers, it is preferably less than 100°C, more preferably 90°C or lower, even more preferably 80°C or lower, still more preferably 70°C or lower, and even more preferably 60°C or lower. The temperature during treatment with a fiber treatment agent containing component (B) (the temperature of the fiber treatment agent) is preferably 20°C or higher and lower than 100°C, more preferably 20°C or higher and 90°C or lower, even more preferably 25°C or higher and 80°C or lower, still more preferably 25°C or higher and 70°C or lower, and even more preferably 30°C or higher and 60°C or lower. When treating with a heated fiber treatment agent, the regenerated collagen fibers or undried regenerated collagen fibers may be immersed in the heated fiber treatment agent, or the regenerated collagen fibers or undried regenerated collagen fibers may be immersed in a cold fiber treatment agent and then the fiber treatment agent may be heated.

[0155] The treatment time (immersion time) with the fiber treatment agent containing component (B) is preferably 15 minutes or more, more preferably 30 minutes or more, even more preferably 1 hour or more, and even more preferably 3 hours or more from the viewpoint of improving the treatment effect, and is preferably 48 hours or less, more preferably 33 hours or less, and even more preferably 20 hours or less from the viewpoint of suppressing damage to the fiber. The treatment time (immersion time) with the fiber treatment agent containing component (B) is preferably 15 minutes to 48 hours, more preferably 30 minutes to 33 hours, even more preferably 1 hour to 20 hours, and even more preferably 3 hours to 20 hours.

[0156] Treatment with the fiber treatment agent containing component (B) is preferably carried out in an environment in which evaporation of water is suppressed. Specific means for suppressing evaporation of water include covering the container of the fiber treatment agent in which the fibers are immersed with a film-like substance, cap, lid, or the like made of a material that is impermeable to water vapor.

[0157] After treatment with the fiber treatment agent, the resulting modified regenerated collagen fibers are preferably washed with water, for example, by washing with running water for 10 minutes to 4 hours.

[0158] When component (B2) is used as component (B), the treatment with the fiber treatment agent containing component (B2) may be carried out two or more times. Specifically, it is preferable to carry out the following steps (1) and (2) in this order two or more times. (1) A step of immersing regenerated collagen fibers or undried regenerated collagen fibers obtained by treatment with a fiber treatment agent containing component (C) in a fiber treatment agent containing component (B2). (2) A step of removing the fibers immersed in the fiber treatment agent in (1) and rinsing them with water.

[0159] From the viewpoint of improving the treatment effect, the treatment conditions for the first treatment and the second and subsequent treatments are more preferably within the following ranges, with the other points remaining the same as above. In the first treatment, the pH at 25°C of the fiber treatment agent used in step (1) is preferably 4.5 or higher, more preferably 5.0 or higher, and is preferably 7.5 or lower, more preferably 7.0 or lower, and even more preferably 6.5 or lower, from the viewpoints of improving penetration into the fiber and suppressing damage to the fiber. In the first treatment, the pH at 25°C of the fiber treatment agent used in step (1) is preferably 4.5 or higher and 7.5 or lower, more preferably 5.0 or higher and 7.0 or lower, and even more preferably 5.0 or higher and 6.5 or lower. In the first treatment, the treatment time (immersion time) in step (1) is preferably 3 hours or more, more preferably 4 hours or more, and even more preferably 6 hours or more from the viewpoint of improving the treatment effect, and is preferably 48 hours or less, more preferably 33 hours or less, and even more preferably 20 hours or less from the viewpoint of suppressing damage to the fiber. In the first treatment, the treatment time (immersion time) in step (1) is preferably 3 hours or more and 48 hours or less, more preferably 4 hours or more and 33 hours or less, and even more preferably 6 hours or more and 20 hours or less.

[0160] In the second or subsequent treatments, the pH at 25°C of the fiber treatment agent used in step (1) is preferably 3.0 or higher, more preferably 3.5 or higher, and is preferably 6.0 or lower, more preferably 5.5 or lower, even more preferably 5.0 or lower, and still more preferably less than 4.5, from the viewpoint of improving the treatment effect. In the second or subsequent treatments, the pH at 25°C of the fiber treatment agent used in step (1) is preferably 3.0 or higher and 6.0 or lower, more preferably 3.0 or higher and 5.5 or lower, even more preferably 3.5 or higher and 5.0 or lower, and still more preferably 3.5 or higher and lower than 4.5. In the second or subsequent treatments, the treatment time (immersion time) in step (1) is preferably 15 minutes or more, more preferably 30 minutes or more, from the viewpoint of improving the treatment effect, and is preferably 5 hours or less, more preferably 3 hours or less, and even more preferably 2 hours or less, from the viewpoint of suppressing damage to the fibers. In the second or subsequent treatments, the treatment time (immersion time) in step (1) is preferably 15 minutes or more and 5 hours or less, more preferably 15 minutes or more and 3 hours or less, and even more preferably 30 minutes or more and 2 hours or less.

[0161] The number of treatments with the fiber treatment agent containing component (B2) is preferably 2 to 5 times, more preferably 2 to 3 times, from the viewpoint of improving the treatment effect and productivity. After the above treatment, the resulting modified regenerated collagen fibers are preferably dried. The drying temperature is preferably 40°C or higher, more preferably 50°C or higher, from the viewpoint of improving the drying rate, and is preferably 100°C or lower, more preferably 80°C or lower, from the viewpoint of suppressing damage to the fibers. The drying time is preferably 15 minutes or longer, more preferably 30 minutes or longer, and from the viewpoint of suppressing damage to the fibers, is preferably 48 hours or shorter, more preferably 33 hours or shorter, and even more preferably 20 hours or shorter.

[0162] By carrying out the above modification treatment, component (B) penetrates into the regenerated collagen fibers. Furthermore, when treatment is carried out with a fiber treatment agent containing component (C), component (B) is strongly coordinated to the polyvalent metal in the fibers. When modified regenerated collagen fibers are dyed using the dye composition of the present invention, the oxidation dye intermediate (A) and its reaction products interact with components (B) and (C) and are more likely to remain within the modified regenerated collagen fibers, which is thought to further improve fastness.

[0163] The regenerated collagen fibers to be dyed with the dye composition of the present invention may be fibers that contain at least a portion of the modified regenerated collagen fibers, or may be fibers consisting solely of modified regenerated collagen fibers. From the viewpoint of further improving fastness, the regenerated collagen fibers to be dyed with the dye composition of the present invention are preferably fibers consisting solely of modified regenerated collagen fibers.

[0164] [Dyeing method] The present invention provides a method for dyeing regenerated collagen fibers, comprising the steps of: The dyeing method includes the following steps (I) and (II) in this order: The regenerated collagen fibers include modified regenerated collagen fibers containing one or more compounds (B) selected from the group consisting of the following components (B1) and (B2): A method for dyeing regenerated collagen fibers is provided.

[0165] Process (I) A step of mixing at least the first agent and the second agent to prepare a dye composition for regenerated collagen fibers. Here, the first agent contains an oxidation dye intermediate (A) containing one or more selected from the group consisting of the following components (A1) and (A2), an alkaline agent, and water, and the second agent contains hydrogen peroxide and water. Process (II) applying the regenerated collagen fiber dye composition to the regenerated collagen fiber;

[0166] (A1) One or more couplers selected from the group consisting of couplers (A1-1) having a benzene ring, electron-donating groups at the 1st and 3rd positions on the benzene ring, and hydrogen atoms at the 4th and 6th positions; couplers (A1-2) having a pyridine ring, electron-donating groups at the 2nd and 6th positions on the pyridine ring, and hydrogen atoms at the 3rd and 5th positions; and couplers (A1-3) represented by the following general formula (A13):

[0167] [ka]

[0168] (In formula (A13), R 11 is -O-(CH2) n R is a divalent group represented by -O- (n is a number of 2 or more and 10 or less). 12 , R 14 , R 22 and R 24 is an electron-donating group, and R 15 and R 25 is a hydrogen atom. R 13 , R 16 , R 23 and R 26 are each independently a hydrogen atom, an alkyl group, or an electron-donating group.

[0169] (A2) One or more couplers other than the component (A1), selected from the group consisting of couplers (A2-1) having a benzene ring, electron-donating groups at the 1st and 2nd positions on the benzene ring, and hydrogen atoms at two or more of the 3rd to 6th positions, and couplers (A2-2) having a pyridine ring, electron-donating groups at the 2nd and 3rd positions on the pyridine ring, and hydrogen atoms at two or more of the 4th to 6th positions.

[0170] (B1) Benzoic acid or its salts (B2) A copolymer containing a structural unit derived from an unsaturated monomer having a carboxy group and a structural unit derived from an aromatic vinyl compound, the copolymer having an acid value of 100 mgKOH / g or more and a weight average molecular weight of 1500 or more and 15000 or less, or a salt thereof.

[0171] In the following description, the method for dyeing regenerated collagen fibers will also be simply referred to as the "dyeing method of the present invention."

[0172] <Process (I)> In step (I), at least the first agent and the second agent are mixed to prepare a dye composition for regenerated collagen fibers. Here, the first agent contains an oxidation dye intermediate (A) containing one or more selected from the group consisting of the following components (A1) and (A2), an alkaline agent, and water, and the second agent contains hydrogen peroxide and water. (A1) One or more couplers selected from the group consisting of couplers having a benzene ring, electron donating groups at the 1st and 3rd positions on the benzene ring, and hydrogen atoms at the 4th and 6th positions, and couplers having a pyridine ring, electron donating groups at the 2nd and 6th positions on the pyridine ring, and hydrogen atoms at the 3rd and 5th positions (A2) One or more couplers selected from the group consisting of couplers having a benzene ring, electron-donating groups at the 1st and 2nd positions on the benzene ring, and hydrogen atoms at two or more of the 3rd to 6th positions, and couplers having a pyridine ring, electron-donating groups at the 2nd and 3rd positions on the pyridine ring, and hydrogen atoms at two or more of the 4th to 6th positions

[0173] The first and second agents, their mixing ratios, and preferred embodiments are the same as those described for the dye composition for regenerated collagen fibers.

[0174] <Process (II)> In step (II), the regenerated collagen fiber dye composition is applied to the regenerated collagen fibers, which include modified regenerated collagen fibers containing one or more compounds (B) selected from the group consisting of the following components (B1) and (B2):

[0175] (B1) Benzoic acid or its salts (B2) A copolymer containing a structural unit derived from an unsaturated monomer having a carboxy group and a structural unit derived from an aromatic vinyl compound, the copolymer having an acid value of 100 mgKOH / g or more and a weight average molecular weight of 1500 or more and 15000 or less, or a salt thereof.

[0176] The modified regenerated collagen fibers and compound (B) and their preferred embodiments are the same as those described above.

[0177] The method for applying the dye composition for regenerated collagen fibers to regenerated collagen fibers may be any method that can bring the dye composition into contact with the regenerated collagen fibers, and examples thereof include a method of applying the composition to regenerated collagen fibers in a dry or wet state, and a method of immersing regenerated collagen fibers in the composition. Among the above, the method of applying the dye composition to regenerated collagen fibers in a dry state is preferred. From the viewpoint of a balance between dyeability, fastness, and economy, the amount of dye composition applied to the regenerated collagen fibers is preferably a bath ratio (dry mass of regenerated collagen fibers:mass of dye composition) of 1:0.2 to 1:500, where the mass of the fibers after conditioning at 20°C and a relative humidity of 65% for 24 hours is taken as the dry mass. When the dye composition is applied to the regenerated collagen fibers, the amount of the dye composition applied to the regenerated collagen fibers, from the viewpoint of a balance between dyeability and economic efficiency, is preferably 1:0.2 to 1:200, even more preferably 1:0.2 to 1:100, even more preferably 1:0.2 to 1:50, even more preferably 1:0.2 to 1:20, even more preferably 1:0.5 to 1:10, even more preferably 1:0.5 to 1:5, and even more preferably 1:0.8 to 1:3. When the regenerated collagen fibers are immersed in the dye composition, the bath ratio (dry mass of the regenerated collagen fibers:mass of the dye composition) is more preferably 1:2 to 1:500, even more preferably 1:3 to 1:250, even more preferably 1:5 to 1:100, even more preferably 1:10 to 1:50, and even more preferably 1:10 to 1:20.

[0178] In step (II), the dyeing conditions for the fiber for headwear may be set using the mass ratio [(B) / (A)] of the compound (B) in the fiber for headwear to the oxidative dye intermediate (A) in the dye composition as an index. Specifically, for example, step (II) may be carried out under conditions such that the mass ratio [(B) / (A)] of the compound (B) in the fiber for headwear to the oxidative dye intermediate (A) in the dye composition is preferably 3 or more, more preferably 5 or more, and even more preferably 10 or more, from the viewpoints of the compatibility of the oxidative dye intermediate (A) and the storage stability and level dyeing ability of the dye composition; and further, from the viewpoints of dyeability and level dyeing ability, it is preferably 4000 or less, more preferably 2000 or less, even more preferably 1000 or less, even more preferably 500 or less, even more preferably 200 or less, even more preferably 100 or less, even more preferably 50 or less. That is, the mass ratio [(B) / (A)] is preferably 3 or more and 4000 or less, more preferably 3 or more and 2000 or less, even more preferably 3 or more and 1000 or less, still more preferably 5 or more and 500 or less, still more preferably 10 or more and 200 or less, still more preferably 20 or more and 100 or less, and still more preferably 20 or more and 50 or less. Furthermore, the dyeing conditions for the fiber for headwear can be set using the mass ratio [(C) / (A)] of component (C) in the fiber for headwear to the oxidation dye intermediate (A) in the dye composition as an index. Specifically, for example, from the viewpoints of the compatibility of the oxidation dye intermediate (A) and the storage stability and level dyeing ability of the dye composition, the mass ratio [(C) / (A)] of component (C) in the fiber for headwear to the oxidation dye intermediate (A) in the dye composition is preferably 0.3 or more, more preferably 0.5 or more, even more preferably 1.0 or more, and still more preferably 2 or more; and from the viewpoints of dyeability and level dyeing ability, step (II) can be performed under conditions such that the mass ratio is preferably 500 or less, more preferably 200 or less, even more preferably 100 or less, still more preferably 50 or less, even more preferably 20 or less, and still more preferably 10 or less. That is, the mass ratio [(C) / (A)] is preferably 0.3 or more and 500 or less, more preferably 0.3 or more and 200 or less, even more preferably 0.5 or more and 200 or less, still more preferably 0.5 or more and 100 or less, still more preferably 1.0 or more and 50 or less, still more preferably 2 or more and 20 or less, and still more preferably 2 or more and 10 or less.

[0179] In step (II), when the dye composition is applied to the regenerated collagen fibers, the application time is preferably 10 seconds or more, more preferably 20 seconds or more, from the viewpoint of further improving dyeability and fastness, and is preferably 10 minutes or less, more preferably 5 minutes or less, from the viewpoint of improving productivity. The application time when the dye composition is applied to the regenerated collagen fibers is preferably 10 seconds or more and 10 minutes or less, more preferably 20 seconds or more and 5 minutes or less. In step (II), it is preferable to further carry out a step of leaving the dye composition after it has been applied to the regenerated collagen fibers. The leaving time is preferably 1 minute or more, more preferably 3 minutes or more, and even more preferably 5 minutes or more, from the viewpoint of further improving dyeability and fastness, and is preferably 1 hour or less, more preferably 30 minutes or less, from the viewpoint of improving productivity. The leaving time after applying the dye composition to the regenerated collagen fibers is preferably 1 minute or more and 1 hour or less, more preferably 3 minutes or more and 30 minutes or less, and even more preferably 5 minutes or more and 30 minutes or less.

[0180] When regenerated collagen fibers are immersed in the dye composition, the immersion time is preferably 10 seconds or more, more preferably 30 seconds or more, from the viewpoint of further improving dyeability and fastness, and is preferably 3 hours or less, more preferably 2 hours or less, and even more preferably 1 hour or less, from the viewpoint of improving productivity. When regenerated collagen fibers are immersed in the dye composition, the immersion time is preferably 10 seconds or more and 3 hours or less, more preferably 10 seconds or more and 2 hours or less, and even more preferably 30 seconds or more and 1 hour or less.

[0181] The temperature at which step (II) is carried out is not particularly limited, but from the viewpoint of improving the handleability of the dye composition and suppressing thermal shrinkage of the regenerated collagen fibers, it is preferably 40°C or lower, more preferably 35°C or lower. From the viewpoint of further improving dyeability and fastness, it is preferably 5°C or higher, more preferably 10°C or higher. The temperature at which the dye composition is applied to the regenerated collagen fibers is preferably 5°C or higher and 40°C or lower, more preferably 10°C or higher and 35°C or lower.

[0182] (Rinse process) The dyeing method of the present invention preferably includes a step of rinsing the dye composition applied to the regenerated collagen fibers after step (II) (hereinafter simply referred to as the "rinsing step"). The rinsing step is carried out, for example, by rinsing the dye composition applied to the regenerated collagen fibers with water. The temperature of the water is not particularly limited, but warm water at 35 to 45°C is preferred.

[0183] (drying process) The dyeing method of the present invention preferably includes a step of drying the regenerated collagen fibers (hereinafter also simply referred to as a "drying step") after applying the dye composition to the regenerated collagen fibers, or after the rinsing step, if any. The step of drying the regenerated collagen fibers is a step of reducing the moisture content of the regenerated collagen fibers, and includes, for example, towel drying, drying with a hairdryer (cold air or hot air), air drying, and a combination of two or more of these drying treatments to actively reduce the moisture content of the regenerated collagen fibers.

[0184] [Colored modified regenerated collagen fiber] The present invention further provides colored modified regenerated collagen fibers containing the following component (A0) and component (B): (A0) A reaction product of an oxidation dye intermediate (A) containing one or more components selected from the group consisting of the following components (A1) and (A2): (A1) One or more couplers selected from the group consisting of couplers (A1-1) having a benzene ring, electron-donating groups at the 1st and 3rd positions on the benzene ring, and hydrogen atoms at the 4th and 6th positions; couplers (A1-2) having a pyridine ring, electron-donating groups at the 2nd and 6th positions on the pyridine ring, and hydrogen atoms at the 3rd and 5th positions; and couplers (A1-3) represented by the following general formula (A13):

[0185] [ka]

[0186] (In formula (A13), R 11 is -O-(CH2) n R is a divalent group represented by -O- (n is a number of 2 or more and 10 or less). 12 , R 14 , R 22 and R 24 is an electron-donating group, and R 15 and R 25 is a hydrogen atom. R 13 , R 16 , R 23 and R 26are each independently a hydrogen atom, an alkyl group, or an electron-donating group.

[0187] (A2) One or more couplers other than the component (A1), selected from the group consisting of couplers (A2-1) having a benzene ring, electron-donating groups at the 1st and 2nd positions on the benzene ring, and hydrogen atoms at two or more of the 3rd to 6th positions, and couplers (A2-2) having a pyridine ring, electron-donating groups at the 2nd and 3rd positions on the pyridine ring, and hydrogen atoms at two or more of the 4th to 6th positions. (B) one or more compounds selected from the group consisting of the following components (B1) and (B2): (B1) Benzoic acid or its salts (B2) A copolymer containing a structural unit derived from an unsaturated monomer having a carboxy group and a structural unit derived from an aromatic vinyl compound, the copolymer having an acid value of 100 mgKOH / g or more and a weight average molecular weight of 1500 or more and 15000 or less, or a salt thereof.

[0188] The colored modified regenerated collagen fibers are modified regenerated collagen fibers that have been modified with the component (B) and then colored with the component (A0). From the viewpoint of further improving dyeability and fastness, the colored modified regenerated collagen fibers preferably further contain the component (C): a polyvalent metal, or a salt or complex thereof.

[0189] The colored modified regenerated collagen fibers can be obtained by preferably preparing modified regenerated collagen fibers containing one or more compounds (B) selected from the group consisting of component (B1) and component (B2) using the method described above, and then applying the dye composition for regenerated collagen fibers to the modified regenerated collagen fibers to dye them. The modified regenerated collagen fibers can preferably be dyed using the dyeing method of the present invention.

[0190] The colored modified regenerated collagen fiber of the present invention preferably has a controlled mass ratio [(B) / (A)] of the compound (B) in the fiber for headwear products to the oxidation dye intermediate (A) in the dye composition. That is, the mass ratio [(B) / (A)] of the compound (B) in the fiber for head accessories to the oxidation dye intermediate (A) in the dye composition is preferably 3 or more, more preferably 5 or more, and even more preferably 10 or more, from the viewpoints of the blendability of the oxidation dye intermediate (A) and the storage stability and dye levelness of the dye composition, and from the viewpoints of dyeability and dye levelness, is preferably 4000 or less, more preferably 2000 or less, even more preferably 1000 or less, even more preferably 500 or less, even more preferably 200 or less, still more preferably 100 or less, and even more preferably 50 or less. That is, the mass ratio [(B) / (A)] is preferably 3 or more and 4000 or less, more preferably 3 or more and 2000 or less, even more preferably 3 or more and 1000 or less, even more preferably 5 or more and 500 or less, still more preferably 10 or more and 200 or less, still more preferably 20 or more and 100 or less, and even more preferably 20 or more and 50 or less.

[0191] Furthermore, the colored modified regenerated collagen fiber of the present invention preferably has a controlled mass ratio [(C) / (A)] of component (C) in the fiber for headwear products to the oxidation dye intermediate (A) in the dye composition. That is, the mass ratio [(C) / (A)] of the component (C) in the fiber for head accessories to the oxidation dye intermediate (A) in the dye composition is preferably 0.3 or more, more preferably 0.5 or more, even more preferably 1.0 or more, and still more preferably 2 or more, from the viewpoints of the blendability of the oxidation dye intermediate (A) and the storage stability and dye levelness of the dye composition, and from the viewpoints of dyeability and dye levelness, is preferably 500 or less, more preferably 200 or less, even more preferably 100 or less, still more preferably 50 or less, still more preferably 20 or less, and still more preferably 10 or less. That is, the mass ratio [(C) / (A)] is preferably 0.3 or more and 500 or less, more preferably 0.3 or more and 200 or less, even more preferably 0.5 or more and 200 or less, still more preferably 0.5 or more and 100 or less, still more preferably 1.0 or more and 50 or less, still more preferably 2 or more and 20 or less, and still more preferably 2 or more and 10 or less.

[0192] [Fibers for headdress products, headdress products] The present invention further provides fibers for head accessories comprising the colored modified regenerated collagen fibers, and head accessories comprising the fibers. The colored modified regenerated collagen fibers can be suitably used as fibers for head accessories. In this specification, "head accessories" refers to, for example, hair wigs, hairpieces, weaving, hair extensions, braided hair, hair accessories, doll hair, etc. Furthermore, "fibers for head accessories" refers to fibers used in the above-mentioned head accessories. In this application, fibers for head accessories also include human hair. The head accessory product may contain at least a portion of colored modified regenerated collagen fibers, and may also contain colored regenerated collagen fibers and human hair.

[0193] With respect to the above-mentioned embodiments, the present invention discloses the following. <1> A dye composition for regenerated collagen fibers, which is a mixture of at least a first agent and a second agent, The first agent is An oxidation dye intermediate (A) comprising one or more components selected from the group consisting of the following components (A1) and (A2): (A1) One or more couplers selected from the group consisting of couplers (A1-1) having a benzene ring, electron-donating groups at the 1st and 3rd positions on the benzene ring, and hydrogen atoms at the 4th and 6th positions; couplers (A1-2) having a pyridine ring, electron-donating groups at the 2nd and 6th positions on the pyridine ring, and hydrogen atoms at the 3rd and 5th positions; and couplers (A1-3) represented by the following general formula (A13): [ka] (In formula (A13), R 11 is -O-(CH2) n R is a divalent group represented by -O- (n is a number of 2 or more and 10 or less). 12 , R 14 , R 22 and R 24 is an electron-donating group, and R 15 and R 25 is a hydrogen atom. R 13 , R 16 , R23 and R 26 are each independently a hydrogen atom, an alkyl group, or an electron-donating group. (A2) one or more couplers other than the component (A1), selected from the group consisting of couplers (A2-1) having a benzene ring, electron-donating groups at the 1- and 2-positions on the benzene ring, and hydrogen atoms at two or more of the 3- to 6-positions, and couplers (A2-2) having a pyridine ring, electron-donating groups at the 2- and 3-positions on the pyridine ring, and hydrogen atoms at two or more of the 4- to 6-positions, Contains an alkaline agent and water, the second agent contains hydrogen peroxide and water, The regenerated collagen fibers contain one or more compounds (B) selected from the group consisting of the following components (B1) and (B2): (B1) Benzoic acid or its salts (B2) A copolymer containing a structural unit derived from an unsaturated monomer having a carboxy group and a structural unit derived from an aromatic vinyl compound, the copolymer having an acid value of 100 mgKOH / g or more and a weight average molecular weight of 1500 or more and 15000 or less, or a salt thereof; A dye composition for regenerated collagen fibers, comprising modified regenerated collagen fibers containing the above. <2> The coupler (A1-1) preferably contains a compound represented by the following general formula (A11) or a salt thereof: <1> A dye composition for regenerated collagen fibers. [ka] (In formula (A11), R 1 is an electron donating group attached to the carbon atom at position 1, R 2 is a hydrogen atom, alkyl group or electron donating group bonded to the carbon atom at the 2nd position, R 3 is an electron donating group attached to the 3-carbon atom, R 4 is a hydrogen atom, an alkyl group, or an electron-donating group bonded to the carbon atom at the 5-position. 2 and R 3 may be bonded to each other to form a hydrocarbon ring structure having aromaticity. <3> The electron-donating group in general formula (A11) preferably includes one or more selected from the group consisting of a hydroxy group, a hydroxyalkyl group, an alkoxy group, a hydroxyalkoxy group, a primary to tertiary amino group, an alkylamino group, and a hydrocarbon ring structure having aromaticity, more preferably includes one or more selected from the group consisting of a hydroxy group, a hydroxyalkyl group having from 2 to 8 carbon atoms, an alkoxy group having from 1 to 8 carbon atoms, a hydroxyalkoxy group having from 2 to 8 carbon atoms, a primary amino group (-NH2), and an alkylamino group having from 1 to 8 carbon atoms, and even more preferably includes one or more selected from the group consisting of a hydroxy group and a primary amino group (-NH2); The alkyl group preferably contains an alkyl group having 1 to 8 carbon atoms, more preferably an alkyl group having 1 to 3 carbon atoms, and even more preferably a methyl group; The aromatic hydrocarbon ring structure is represented by R 2 and R 3 are bonded to each other to form an aromatic hydrocarbon ring structure, the ring structure preferably contains an aromatic hydrocarbon ring structure having 5 to 8 ring carbon atoms, more preferably contains an aromatic hydrocarbon ring structure having 5 to 6 ring carbon atoms, and even more preferably contains an aromatic hydrocarbon ring structure having 6 ring carbon atoms, <2> A dye composition for regenerated collagen fibers. <4> In the general formula (A11), R 1 is preferably a hydroxy group or a primary amino group (—NH), and R 2 is preferably a hydrogen atom or a methyl group, and R 3 is preferably a hydroxy group or a primary amino group (-NH), or R 2 and R 3 are bonded to each other to form an aromatic hydrocarbon ring structure having six ring carbon atoms, and R 4 is preferably a hydrogen atom or a methyl group, more preferably a hydrogen atom; <2> or <3> A dye composition for regenerated collagen fibers. <5> The compound represented by the general formula (A11) is at least one selected from the group consisting of meta-aminophenol, resorcinol, meta-phenylenediamine, 2-methylresorcinol, 1-naphthol, and salts thereof, and preferably at least one selected from the group consisting of meta-aminophenol, resorcinol, 2-methylresorcinol, 1-naphthol, and salts thereof. <2> ~ <4> Any one of the above dye compositions for regenerated collagen fibers. <6> The coupler (A1-2) preferably contains a compound represented by the following general formula (A12) or a salt thereof: <1> ~ <5> Any one of the above dye compositions for regenerated collagen fibers. [ka] (In formula (A12), R 5 is an electron donating group attached to the 2nd carbon atom, R 6 represents a hydrogen atom, an alkyl group, or an electron-donating group bonded to the 4-carbon atom; R 7 is an electron-donating group attached to the 6-carbon atom.) <7> The electron-donating group in general formula (A12) preferably includes one or more selected from the group consisting of a hydroxy group, a hydroxyalkyl group, an alkoxy group, a hydroxyalkoxy group, a primary to tertiary amino group, and an alkylamino group, more preferably includes one or more selected from the group consisting of a hydroxy group, a hydroxyalkyl group having from 2 to 8 carbon atoms, an alkoxy group having from 1 to 8 carbon atoms, a hydroxyalkoxy group having from 2 to 8 carbon atoms, a primary amino group (-NH2), and an alkylamino group having from 1 to 8 carbon atoms, and even more preferably includes one or more selected from the group consisting of a hydroxy group and a primary amino group (-NH2); The alkyl group preferably contains an alkyl group having 1 to 8 carbon atoms, more preferably contains an alkyl group having 1 to 3 carbon atoms, and even more preferably contains a methyl group. <6> A dye composition for regenerated collagen fibers. <8> In the general formula (A12), R 5 is preferably a hydroxy group or a primary amino group (—NH), and R 6is preferably a hydrogen atom or a methyl group, and R 7 is preferably a primary amino group (—NH), <6> or <7> A dye composition for regenerated collagen fibers. <9> The compound represented by the general formula (A12) contains 2,6-diaminopyridine or a salt thereof. <6> ~ <8> Any one of the above dye compositions for regenerated collagen fibers. <10> In the general formula (A13), R 11 In the formula, n is preferably 2 or more and 8 or less, more preferably 2 or more and 4 or less, R 12 , R 14 , R 22 and R 24 The electron donating group in preferably comprises a hydroxy group or a primary amino group (-NH), more preferably a primary amino group (-NH), R 13 , R 16 , R 23 and R 26 preferably contains a hydrogen atom or a methyl group, more preferably a hydrogen atom; <1> ~ <9> Any one of the above dye compositions for regenerated collagen fibers.

[0194] <11> the coupler represented by general formula (A13) contains 1,3-bis(2,4-diaminophenoxy)propane or a salt thereof; <1> ~ <10> Any one of the above dye compositions for regenerated collagen fibers. <12> The component (A1) preferably contains one or more selected from the group consisting of meta-aminophenol, resorcinol, meta-phenylenediamine, 2-methylresorcinol, 1-naphthol, 2,6-diaminopyridine, 1,3-bis(2,4-diaminophenoxy)propane, and salts thereof, and more preferably contains one or more selected from the group consisting of meta-aminophenol, resorcinol, 2-methylresorcinol, 1-naphthol, and salts thereof. <1> ~ <11> Any one of the above dye compositions for regenerated collagen fibers. <13> The coupler (A2-1) preferably contains a compound represented by the following general formula (A21) or a salt thereof (however, couplers corresponding to the component (A1) are excluded): <1> ~ <12> Any one of the above dye compositions for regenerated collagen fibers. [ka] (In formula (A21), R 31 is an electron donating group attached to the carbon atom at position 1, R 32 is an electron donating group attached to the 2nd carbon atom, R 33 ~R 36 are hydrogen atoms, alkyl groups, or electron-donating groups bonded to the 3-, 4-, 5-, and 6-position carbons, respectively. 33 ~R 36 At least two of these are hydrogen atoms.) <14> The electron-donating group in general formula (A21) preferably includes one or more selected from the group consisting of a hydroxy group, a hydroxyalkyl group, an alkoxy group, a hydroxyalkoxy group, a primary to tertiary amino group, and an alkylamino group, more preferably includes one or more selected from the group consisting of a hydroxy group, a hydroxyalkyl group having from 2 to 8 carbon atoms, an alkoxy group having from 1 to 8 carbon atoms, a hydroxyalkoxy group having from 2 to 8 carbon atoms, a primary amino group (-NH2), and an alkylamino group having from 1 to 8 carbon atoms, and even more preferably includes one or more selected from the group consisting of a hydroxy group, a hydroxyalkoxy group having from 2 to 8 carbon atoms, and a primary amino group (-NH2); The alkyl group preferably contains an alkyl group having 1 to 8 carbon atoms, more preferably contains an alkyl group having 1 to 3 carbon atoms, and even more preferably contains a methyl group. <13> A dye composition for regenerated collagen fibers. <15> In the general formula (A21), R 31 is preferably a hydroxy group, a hydroxyalkoxy group having from 2 to 8 carbon atoms, or a primary amino group (-NH), more preferably a hydroxy group, a hydroxyethoxy group, or a primary amino group (-NH); R 32is preferably a hydroxy group or a primary amino group (-NH), more preferably a primary amino group (-NH), <13> or <14> A dye composition for regenerated collagen fibers. <16> The compound represented by the general formula (A21) contains one or more selected from the group consisting of ortho-aminophenol, 2,4-diaminophenoxyethanol, and salts thereof. <13> ~ <15> Any one of the above dye compositions for regenerated collagen fibers. <17> The coupler (A2-2) preferably contains a compound represented by the following general formula (A22) or a salt thereof: <1> ~ <16> Any one of the above dye compositions for regenerated collagen fibers. [ka] (In formula (A22), R 37 is an electron donating group attached to the 2nd carbon atom, R 38 is an electron donating group attached to the 3-carbon atom. 39 ~R 41 are hydrogen atoms, alkyl groups, or electron-donating groups bonded to the 4-, 5-, and 6-position carbons, respectively. 39 ~R 41 At least two of these are hydrogen atoms.) <18> In the general formula (A22), R 37 is preferably a hydroxy group or a primary amino group (—NH), and R 38 is preferably a hydroxy group or a primary amino group (-NH), more preferably a primary amino group (-NH), and R 39 ~R 41 are each independently preferably a hydrogen atom or a methyl group, more preferably R 39 ~R 41 are all hydrogen atoms, <17> A dye composition for regenerated collagen fibers. <19> The compound represented by the general formula (A22) includes 2,3-diaminopyridine, 2-amino-3-hydroxypyridine, or a salt thereof. <17> or <18> A dye composition for regenerated collagen fibers. <20> The component (A2) preferably contains a coupler (A2-1), more preferably one or more selected from the group consisting of ortho-aminophenol, 2,4-diaminophenoxyethanol, and salts thereof. <1> ~ <19> Any one of the above dye compositions for regenerated collagen fibers.

[0195] <21> The oxidation dye intermediate (A) preferably contains a component (A1), and more preferably contains one or more selected from the group consisting of meta-aminophenol, resorcinol, meta-phenylenediamine, 2-methylresorcinol, 1-naphthol, 2,6-diaminopyridine, 1,3-bis(2,4-diaminophenoxy)propane, and salts thereof. <1> ~ <20> Any one of the above dye compositions for regenerated collagen fibers. <22> The oxidation dye intermediate (A) preferably contains a coupler (A1-1), more preferably contains one or more selected from the group consisting of meta-aminophenol, resorcinol, 2-methylresorcinol, 1-naphthol, and salts thereof. <1> ~ <20> Any one of the above dye compositions for regenerated collagen fibers. <23> The total content of the component (A1) and the component (A2) in the oxidation dye intermediate (A) is preferably 30% by mass or more, more preferably 40% by mass or more, and may be 100% by mass or less, 90% by mass or less, 80% by mass or less, 70% by mass or less, or 60% by mass or less. <1> ~ <22> Any one of the above dye compositions for regenerated collagen fibers. <24> The content of the component (A1) in the oxidation dye intermediate (A) is preferably 30% by mass or more, more preferably 40% by mass or more, and may be 100% by mass or less, 90% by mass or less, 80% by mass or less, 70% by mass or less, or 60% by mass or less. <1> ~ <23> Any one of the above dye compositions for regenerated collagen fibers. <25> the oxidation dye intermediate (A) further contains a component (A3): a precursor, and the precursor contains at least one selected from the group consisting of paraphenylenediamine, toluene-2,5-diamine, orthochloroparaphenylenediamine, N-phenylparaphenylenediamine, N,N-bis(hydroxyethyl)paraphenylenediamine, 3-methyl-4-aminophenol, 2-hydroxyethylparaphenylenediamine, paraaminophenol, paramethylaminophenol, 4-amino-metacresol, and salts thereof, preferably at least one selected from the group consisting of toluene-2,5-diamine, paraaminophenol, 4-amino-metacresol, 1-hydroxyethyl-4,5-diaminopyrazole, and salts thereof; <1> ~ <24> Any one of the above dye compositions for regenerated collagen fibers. <26> The content of the component (A3) in the oxidation dye intermediate (A) is preferably 20% by mass or more and 70% by mass or less, more preferably 30% by mass or more and 65% by mass or less, and even more preferably 40% by mass or more and 60% by mass or less. <25> A dye composition for regenerated collagen fibers. <27> The content of couplers other than the components (A1) and (A2) in the oxidation dye intermediate (A) is preferably 30% by mass or less, more preferably 20% by mass or less, even more preferably 10% by mass or less, still more preferably 5% by mass or less, and even more preferably 2% by mass or less, and may be 0% by mass. <1> ~ <26> Any one of the above dye compositions for regenerated collagen fibers. <28> The molecular weight of the oxidation dye intermediate (A) is preferably 95 or more and 500 or less, more preferably 100 or more and 300 or less, and even more preferably 105 or more and 200 or less, as a non-dissociated type. <1> ~ <27> Any one of the above dye compositions for regenerated collagen fibers. <29> The alkaline agent preferably contains one or more selected from the group consisting of ammonia, alkanolamine, alkylamine, aralkylamine, sodium hydroxide, and potassium hydroxide, and more preferably contains one or more selected from the group consisting of ammonia and alkanolamine. <1> ~ <28> Any one of the above dye compositions for regenerated collagen fibers. <30> The content of component (A) in the first agent is preferably 0.01% by mass or more and 5.0% by mass or less, more preferably 0.02% by mass or more and 3.0% by mass or less, even more preferably 0.05% by mass or more and 3.0% by mass or less, still more preferably 0.1% by mass or more and 3.0% by mass or less, still more preferably 0.2% by mass or more and 3.0% by mass or less, still more preferably 0.3% by mass or more and 3.0% by mass or less, and still more preferably 0.5% by mass or more and 2.0% by mass or less, <1> ~ <29> Any one of the above dye compositions for regenerated collagen fibers.

[0196] <31> The total content of component (A1) and component (A2) in the first agent is preferably 0.01% by mass or more and 5.0% by mass or less, more preferably 0.02% by mass or more and 3.0% by mass or less, even more preferably 0.05% by mass or more and 2.0% by mass or less, still more preferably 0.1% by mass or more and 1.5% by mass or less, still more preferably 0.2% by mass or more and 1.5% by mass or less, and still more preferably 0.25% by mass or more and 1.0% by mass or less. <1> ~ <30> Any one of the above dye compositions for regenerated collagen fibers. <32> The content of the alkaline agent in the first agent is preferably 0.01% by mass or more and 10% by mass or less, more preferably 0.1% by mass or more and 7.5% by mass or less, even more preferably 0.5% by mass or more and 7.5% by mass or less, and still more preferably 1.0% by mass or more and 5.0% by mass or less. <1> ~ <31> Any one of the above dye compositions for regenerated collagen fibers. <33> The content of water in the first agent is preferably 70% by mass or more, more preferably 80% by mass or more, even more preferably 85% by mass or more, and is preferably 99.98% by mass or less. <1> ~ <32> Any one of the above dye compositions for regenerated collagen fibers. <34> The pH of the first agent is preferably 6 or more and 12.0 or less, more preferably 8 or more and 11.5 or less, and even more preferably 10 or more and 11.0 or less. <1> ~ <33> Any one of the above dye compositions for regenerated collagen fibers. <35> The dosage form of the first agent is liquid, paste, cream, gel, foam, spray, or wax, preferably liquid. <1> ~ <34> Any one of the above dye compositions for regenerated collagen fibers. <36> The content of hydrogen peroxide in the second agent is preferably 0.1% by mass or more and 10% by mass or less, more preferably 0.5% by mass or more and 10% by mass or less, and even more preferably 1.0% by mass or more and 8.0% by mass or less. <1> ~ <35> Any one of the above dye compositions for regenerated collagen fibers. <37> The pH of the second agent is preferably 2.5 or more and 6 or less, more preferably 2.5 or more and 5 or less, and even more preferably 3.0 or more and 4 or less. <1> ~ <36> Any one of the above dye compositions for regenerated collagen fibers. <38> The dosage form of the second agent is liquid, paste, cream, gel, foam, spray, or wax, and is preferably liquid. <1> ~ <37> Any one of the above dye compositions for regenerated collagen fibers. <39> The mixing ratio of the first agent to the second agent (mass ratio) is preferably in the range of 1:0.1 to 1:10, more preferably 1:0.2 to 1:5, and even more preferably 1:0.5 to 1:3. <1> ~ <38> Any one of the above dye compositions for regenerated collagen fibers. <40> the pH of the composition after mixing the first agent and the second agent is preferably 3.0 or more and 7.5 or less, more preferably 3.5 or more and 7.0 or less, and even more preferably 4.0 or more and 6.5 or less at 25°C; <1> ~ <39> Any one of the above dye compositions for regenerated collagen fibers.

[0197] <41> The content of component (A) or a reaction product of component (A) in the dye composition is preferably 0.005% by mass or more and 3.0% by mass or less, more preferably 0.01% by mass or more and 3.0% by mass or less, even more preferably 0.02% by mass or more and 3.0% by mass or less, still more preferably 0.03% by mass or more and 2.0% by mass or less, still more preferably 0.05% by mass or more and 2.0% by mass or less, still more preferably 0.1% by mass or more and 2.0% by mass or less, and still more preferably 0.2% by mass or more and 1.0% by mass or less, <1> ~ <40> Any one of the above dye compositions for regenerated collagen fibers. <42> The content of the alkaline agent in the dye composition is preferably 0.005% by mass or more and 5.0% by mass or less, more preferably 0.01% by mass or more and 3.5% by mass or less, even more preferably 0.1% by mass or more and 3.5% by mass or less, still more preferably 0.5% by mass or more and 3.5% by mass or less, and still more preferably 1.0% by mass or more and 2.5% by mass or less, <1> ~ <41> Any one of the above dye compositions for regenerated collagen fibers. <43> The content of water in the dye composition is preferably 70% by mass or more, more preferably 80% by mass or more, even more preferably 85% by mass or more, and is preferably 99.9% by mass or less. <1> ~ <42> Any one of the above dye compositions for regenerated collagen fibers. <44> The component (B1) contains one or more selected from the group consisting of benzoic acid, sodium benzoate, and potassium benzoate, and preferably contains one or more selected from the group consisting of benzoic acid and sodium benzoate. <1> ~ <43> Any one of the above dye compositions for regenerated collagen fibers. <45> the component (B2) comprises a copolymer containing structural units derived from one or more selected from the group consisting of unsaturated monocarboxylic acids and unsaturated dicarboxylic acids, and structural units derived from an aromatic vinyl compound, preferably one or more selected from the group consisting of styrene-maleic acid copolymer, styrene-acrylic acid copolymer, styrene-methacrylic acid copolymer, vinylbenzoic acid-maleic acid copolymer, vinylbenzoic acid-acrylic acid copolymer, vinylbenzoic acid-methacrylic acid copolymer, and styrene-4-vinylbenzoic acid copolymer, more preferably a styrene-maleic acid copolymer; <1> ~ <44> Any one of the above dye compositions for regenerated collagen fibers. <46> In the component (B2), the molar ratio (u1 / u2) of the structural unit (u1) derived from the unsaturated monomer having a carboxy group to the structural unit (u2) derived from the aromatic vinyl compound monomer is preferably 1 / 5 to 5 / 1, more preferably 1 / 3 to 3 / 1, and even more preferably 1 / 2 to 2 / 1. <1> ~ <45> Any one of the above dye compositions for regenerated collagen fibers. <47> The acid value of the component (B2) is preferably 100 mgKOH / g or more and 1000 mgKOH / g or less, more preferably 200 mgKOH / g or more and 800 mgKOH / g or less, even more preferably 200 mgKOH / g or more and 600 mgKOH / g or less, still more preferably 300 mgKOH / g or more and 600 mgKOH / g or less, and still more preferably 400 mgKOH / g or more and 600 mgKOH / g or less. <1> ~ <46> Any one of the above dye compositions for regenerated collagen fibers. <48> The weight average molecular weight of the component (B2) is preferably 3,000 or more and 15,000 or less, more preferably 5,000 or more and 15,000 or less, even more preferably 6,000 or more and 15,000 or less, and still more preferably 6,000 or more and 10,000 or less. <1> ~ <47> Any one of the above dye compositions for regenerated collagen fibers. <49> The compound (B) preferably contains one or more selected from the group consisting of benzoic acid, sodium benzoate, and a styrene-maleic acid copolymer, and more preferably contains a styrene-maleic acid copolymer. <1> ~ <48> Any one of the above dye compositions for regenerated collagen fibers. <50> The content of compound (B) in the modified regenerated collagen fibers is preferably 0.1% by mass or more and 70% by mass or less, more preferably 0.5% by mass or more and 65% by mass or less, even more preferably 1.0% by mass or more and 60% by mass or less, still more preferably 3.0% by mass or more and 55% by mass or less, even more preferably 5.0% by mass or more and 50% by mass or less, still more preferably 10% by mass or more and 45% by mass or less, still more preferably 15% by mass or more and 40% by mass or less, and still more preferably 20% by mass or more and 40% by mass or less, <1> ~ <49> Any one of the above dye compositions for regenerated collagen fibers.

[0198] <51> The modified regenerated collagen fibers further contain a polyvalent metal, a salt thereof, or a complex thereof as component (C). <1> ~ <50> Any one of the above dye compositions for regenerated collagen fibers. <52> The component (C) contains one or more polyvalent metals selected from the group consisting of calcium, magnesium, strontium, barium, zinc, chromium, aluminum, titanium, zirconium, tin, lead, antimony, iron, and copper, or salts thereof, or complexes thereof, preferably one or more polyvalent metals selected from the group consisting of aluminum, zirconium, and titanium, or salts thereof, or complexes thereof, and more preferably aluminum, or salts thereof, or complexes thereof; <1> ~ <51> Any one of the above dye compositions for regenerated collagen fibers. <53> The content of component (C) in the modified regenerated collagen fibers is preferably 0.1% by mass or more and 40% by mass or less, more preferably 0.5% by mass or more and 30% by mass or less, even more preferably 1.0% by mass or more and 20% by mass or less, and even more preferably 2% by mass or more and 10% by mass or less, in terms of the amount of metal elements. <1> ~ <52> Any one of the above dye compositions for regenerated collagen fibers. <54> A method for dyeing regenerated collagen fibers, comprising: The regenerated collagen fibers contain one or more compounds (B) selected from the group consisting of the following components (B1) and (B2): (B1) Benzoic acid or its salts (B2) A copolymer containing a structural unit derived from an unsaturated monomer having a carboxy group and a structural unit derived from an aromatic vinyl compound, the copolymer having an acid value of 100 mgKOH / g or more and a weight average molecular weight of 1500 or more and 15000 or less, or a salt thereof; The modified regenerated collagen fiber contains The present invention provides a method for dyeing regenerated collagen fibers, which comprises the following steps (I) and (II) in this order: Step (I): Mixing at least the first agent and the second agent to prepare a dye composition for regenerated collagen fibers. Here, the first agent is An oxidation dye intermediate (A) comprising one or more components selected from the group consisting of the following components (A1) and (A2): (A1) One or more couplers selected from the group consisting of couplers (A1-1) having a benzene ring, electron-donating groups at the 1st and 3rd positions on the benzene ring, and hydrogen atoms at the 4th and 6th positions; couplers (A1-2) having a pyridine ring, electron-donating groups at the 2nd and 6th positions on the pyridine ring, and hydrogen atoms at the 3rd and 5th positions; and couplers (A1-3) represented by the following general formula (A13): [ka] (In formula (A13), R 11 is -O-(CH2) n R is a divalent group represented by -O- (n is a number of 2 or more and 10 or less). 12 , R 14 , R 22 and R 24 is an electron-donating group, and R 15 and R 25 is a hydrogen atom. R 13 , R 16 , R 23 and R 26are each independently a hydrogen atom, an alkyl group, or an electron-donating group. (A2) one or more couplers other than the component (A1), selected from the group consisting of couplers (A2-1) having a benzene ring, electron-donating groups at the 1- and 2-positions on the benzene ring, and hydrogen atoms at two or more of the 3- to 6-positions, and couplers (A2-2) having a pyridine ring, electron-donating groups at the 2- and 3-positions on the pyridine ring, and hydrogen atoms at two or more of the 4- to 6-positions, Contains an alkaline agent and water, The second agent contains hydrogen peroxide and water. Step (II): Applying the regenerated collagen fiber dye composition to the regenerated collagen fiber. <55> In the step (II), the method of applying the dye composition to the regenerated collagen fibers includes a method of applying the composition to the regenerated collagen fibers in a dry or wet state, or a method of immersing the regenerated collagen fibers in the composition, and preferably includes a method of applying the composition to the regenerated collagen fibers in a dry state, or a method of immersing the regenerated collagen fibers in a dry state. <54> Dyeing method. <56> In the step (II), the amount of the dye composition applied to the regenerated collagen fibers is preferably 1:0.2 to 1:500 in terms of bath ratio (dry mass of regenerated collagen fibers:mass of dye composition), when the mass of the fibers after conditioning for 24 hours at 20°C and a relative humidity of 65% is taken as the dry mass. <54> or <55> Dyeing method. <57> In the step (II), when the dye composition is applied to the regenerated collagen fibers, the amount of the dye composition applied to the regenerated collagen fibers, when the mass of the fibers after conditioning at 20°C and a relative humidity of 65% for 24 hours is taken as the dry mass, is preferably 1:0.2 to 1:200 in terms of the bath ratio (dry mass of regenerated collagen fibers:mass of dye composition), still more preferably 1:0.2 to 1:100, still more preferably 1:0.2 to 1:50, still more preferably 1:0.2 to 1:20, more preferably 1:0.5 to 1:10, still more preferably 1:0.5 to 1:5, and still more preferably 1:0.8 to 1:3. <56> Dyeing method. <58> In the step (II), when the regenerated collagen fibers are immersed in the dye composition, the bath ratio (dry mass of regenerated collagen fibers:mass of dye composition) is more preferably 1:2 to 1:500, even more preferably 1:3 to 1:250, still more preferably 1:5 to 1:100, still more preferably 1:10 to 1:50, and still more preferably 1:10 to 1:20, when the mass of the fibers after conditioning at 20°C and a relative humidity of 65% for 24 hours is taken as the dry mass. <56> Dyeing method. <59> In the step (II), when the dye composition is applied to the regenerated collagen fibers, the application time is preferably 10 seconds or more and 10 minutes or less, more preferably 20 seconds or more and 5 minutes or less. <55> ~ <58> One of the following dyeing methods. <60> In the step (II), after the dye composition is applied to the regenerated collagen fibers, a step of leaving the composition to stand is further carried out, and the leaving time is preferably 1 minute or more and 1 hour or less, more preferably 3 minutes or more and 30 minutes or less, and even more preferably 5 minutes or more and 30 minutes or less. <55> ~ <57> , <59> One of the following dyeing methods.

[0199] <61> In the step (II), when the regenerated collagen fibers are immersed in the dye composition, the immersion time is preferably from 10 seconds to 3 hours, more preferably from 10 seconds to 2 hours, and even more preferably from 30 seconds to 1 hour. <55> , <56> , <58> One of the following dyeing methods. <62> In the step (II), the temperature at which the dye composition is applied to the regenerated collagen fibers is preferably 5°C or higher and 40°C or lower, more preferably 10°C or higher and 35°C or lower. <54> ~ <61> One of the following dyeing methods. <63> After carrying out the step (II), a step of rinsing the dye composition applied to the regenerated collagen fibers is included. <54> ~ <62> One of the following dyeing methods. <64> a step of drying the regenerated collagen fibers after applying the dye composition to the regenerated collagen fibers, and after performing a rinsing step, if any; <54> ~ <63> One of the following dyeing methods. <65> A colored modified regenerated collagen fiber containing the following component (A0) and component (B): (A0) A reaction product of an oxidation dye intermediate (A) containing one or more components selected from the group consisting of the following components (A1) and (A2): (A1) One or more couplers selected from the group consisting of couplers (A1-1) having a benzene ring, electron-donating groups at the 1st and 3rd positions on the benzene ring, and hydrogen atoms at the 4th and 6th positions; couplers (A1-2) having a pyridine ring, electron-donating groups at the 2nd and 6th positions on the pyridine ring, and hydrogen atoms at the 3rd and 5th positions; and couplers (A1-3) represented by the following general formula (A13): [ka] (In formula (A13), R 11 is -O-(CH2) n R is a divalent group represented by -O- (n is a number of 2 or more and 10 or less). 12 , R 14 , R 22 and R 24 is an electron-donating group, and R 15 and R 25 is a hydrogen atom. R 13 , R 16 , R 23 and R 26are each independently a hydrogen atom, an alkyl group, or an electron-donating group. (A2) One or more couplers other than the component (A1), selected from the group consisting of couplers (A2-1) having a benzene ring, electron-donating groups at the 1st and 2nd positions on the benzene ring, and hydrogen atoms at two or more of the 3rd to 6th positions, and couplers (A2-2) having a pyridine ring, electron-donating groups at the 2nd and 3rd positions on the pyridine ring, and hydrogen atoms at two or more of the 4th to 6th positions. (B) one or more compounds selected from the group consisting of the following components (B1) and (B2): (B1) Benzoic acid or its salts (B2) A copolymer containing a structural unit derived from an unsaturated monomer having a carboxy group and a structural unit derived from an aromatic vinyl compound, the copolymer having an acid value of 100 mgKOH / g or more and a weight average molecular weight of 1500 or more and 15000 or less, or a salt thereof. <66> The colored modified regenerated collagen fiber further contains the component (C): a polyvalent metal, a salt thereof, or a complex thereof. <65> Colored modified regenerated collagen fiber. <67> <65> or <66> A fiber for headwear products, comprising colored modified regenerated collagen fiber. <68> <65> or <66> A headwear product comprising colored modified regenerated collagen fibers. <69> The headwear product is a hair wig, a hairpiece, a weaving, a hair extension, a braided hair, a hair accessory, or a doll hair. <67> Fibers for head accessories, or <68> Head ornament products.

[0200] <70> A dye composition for regenerated collagen fibers, which is a mixture of at least a first agent and a second agent, the first agent contains one or more oxidation dye intermediates (A) selected from meta-aminophenol, resorcinol, meta-phenylenediamine, 2-methylresorcinol, 1-naphthol, 2,6-diaminopyridine, 1,3-bis(2,4-diaminophenoxy)propane, and salts thereof, an alkali agent, and water; the second agent contains hydrogen peroxide and water, The regenerated collagen fibers include modified regenerated collagen fibers containing one or more compounds (B) selected from the group consisting of the following components (B1) and (B2): Dyeing composition for regenerated collagen fibers. (B1) Benzoic acid or its salts (B2) A styrene-maleic acid copolymer or a salt thereof having an acid value of 200 mgKOH / g or more and 600 mgKOH / g or less and a weight average molecular weight of 3,000 or more and 15,000 or less.

[0201] <71> A method for dyeing regenerated collagen fibers, comprising: The method includes the following steps (I) and (II) in this order: The regenerated collagen fibers include modified regenerated collagen fibers containing one or more compounds (B) selected from the group consisting of the following components (B1) and (B2): A method for dyeing regenerated collagen fibers. Step (I): Mixing at least the first agent and the second agent to prepare a dye composition for regenerated collagen fibers. wherein the first agent contains one or more oxidation dye intermediates (A) selected from meta-aminophenol, resorcinol, meta-phenylenediamine, 2-methylresorcinol, 1-naphthol, 2,6-diaminopyridine, 1,3-bis(2,4-diaminophenoxy)propane, and salts thereof, an alkali agent, and water; The second agent contains hydrogen peroxide and water. Step (II): Applying the regenerated collagen fiber dye composition to the regenerated collagen fiber. (B1) Benzoic acid or its salts (B2) A styrene-maleic acid copolymer or a salt thereof having an acid value of 200 mgKOH / g or more and 600 mgKOH / g or less and a weight average molecular weight of 3,000 or more and 15,000 or less.

[0202] <72> A colored modified regenerated collagen fiber containing the following component (A0) and component (B): A colored modified regenerated collagen fiber obtained by dyeing a modified regenerated collagen fiber containing component (B) using a dye composition prepared by mixing at least a first agent containing an oxidation dye intermediate (A), an alkaline agent, and water, and a second agent containing hydrogen peroxide and water. (A0) Reaction products of one or more oxidation dye intermediates (A) selected from meta-aminophenol, resorcinol, meta-phenylenediamine, 2-methylresorcinol, 1-naphthol, 2,6-diaminopyridine, 1,3-bis(2,4-diaminophenoxy)propane, and salts thereof. (B) one or more compounds selected from the group consisting of the following components (B1) and (B2): (B1) Benzoic acid or its salts (B2) A styrene-maleic acid copolymer or a salt thereof having an acid value of 200 mgKOH / g or more and 600 mgKOH / g or less and a weight average molecular weight of 3,000 or more and 15,000 or less.

[0203] <73> The modified regenerated collagen fiber contains, as component (B2), a styrene-maleic acid copolymer or a salt thereof having an acid value of 200 mgKOH / g or more and 600 mgKOH / g or less and a weight-average molecular weight of 6,000 or more and 15,000 or less. <70> A dye composition comprising the compound <71> or <72> Colored modified regenerated collagen fiber. <74> The modified regenerated collagen fiber contains, as component (B2), a styrene-maleic acid copolymer or a salt thereof having an acid value of 400 mgKOH / g or more and 600 mgKOH / g or less and a weight-average molecular weight of 6,000 or more and 10,000 or less. <70> or <73> A dye composition comprising the compound <71> or <73> or <72> or <73> Colored modified regenerated collagen fiber.

[0204] <75> the mass ratio [{(A1) + (A2)} / hydrogen peroxide] of the total content of the oxidative dye intermediate (A) in the first agent to the hydrogen peroxide in the second agent is 0.03 or more and 1.0 or less; <70> and <73> ~ <74> Any one of the dye compositions <71> and <73> ~ <74> One of the following dyeing methods. <76> The content of compound (B) in the modified regenerated collagen fiber is 20% by mass or more and 40% by mass or less. <70> and <73> ~ <75> any one of the dye compositions <71> and <73> ~ <75> Any one of the staining methods, or <72> ~ <75> Any one of the colored modified regenerated collagen fibers. <77> the mass ratio [(B) / (A)] of the compound (B) in the fiber for headwear to the oxidation dye intermediate (A) in the dye composition is 20 or more and 100 or less; <70> and <73> ~ <76> any one of the dye compositions <71> and <73> ~ <76> Any one of the staining methods, or <72> ~ <76> Any one of the colored modified regenerated collagen fibers.

[0205] <78> The modified regenerated collagen fibers contain aluminum or a salt or complex thereof as component (C). <70> and <73> ~ <77> Any one of the dye compositions <71> and <73> ~ <77> Any one of the staining methods, or <72> ~ <77> Any one of the colored modified regenerated collagen fibers. <79> The content of component (C) in the modified regenerated collagen fiber is 2.0% by mass or more and 10% by mass or less in terms of the amount of metal element, the dye composition of <78>, the dyeing method of <78>, or the colored modified regenerated collagen fiber of <78>. <80> The mass ratio [(C) / (A)] of component (C) in the fiber for headgear products to the oxidation dye intermediate (A) in the dye composition is 2 or more and 20 or less, the dye composition of <78> or <79>, the dyeing method of <78> or <79>, or the colored modified regenerated collagen fiber of <78> or <79>.

[0206] <81> A headgear product containing the colored modified regenerated collagen fiber of any one of <72> to <80>.

Examples

[0207] Hereinafter, the present invention will be described by way of examples, but the present invention is not limited to the scope of the examples. In this example, various measurements and evaluations were performed by the following methods.

[0208] <pH measurement> The pH at 25 °C was measured using a pH meter (F-72, manufactured by Horiba, Ltd.).

[0209] <Quantification of benzoic acid in the modified regenerated collagen fiber> In this specification, the quantification of benzoic acid contained in the modified regenerated collagen fiber B1 obtained in Production Example 2 was performed by the following method. · Reagents 6N hydrochloric acid: Titrant for volumetric analysis, manufactured by Kanto Chemical Co., Inc. Sodium acetate: Special grade, manufactured by Fujifilm Wako Pure Chemical Corporation Acetic acid: Special grade, manufactured by Fujifilm Wako Pure Chemical Corporation [[ID=4,1]]Acetonitrile: For LC / MS, manufactured by Kanto Chemical Co., Inc. Sodium benzoate: Special grade, manufactured by Fujifilm Wako Pure Chemical Corporation Ultra-pure water: Milli-Q water produced by an ultra-pure water production apparatus, manufactured by Millipore [[ID=4,7]]· Quantification method The sample (modified regenerated collagen fiber B1) was conditioned at 20°C and 65% relative humidity for 24 hours, then finely chopped. Approximately 10 mg of the sample was precisely weighed, and 3 mL of 6N hydrochloric acid was added. The mixture was then heated and dissolved at 50°C for 15 hours. After cooling, the mixture was filtered to prepare the sample solution. Separately, sodium benzoate was dissolved in the mobile phase to prepare a benzoic acid concentration of 0.1 to 100 μg / mL. This was used as the standard solution for constructing the calibration curve. Liquid chromatography (HPLC) measurements were performed using the sample solution and the standard solution, and the amount of benzoic acid was calculated from the ratio of the peak area of ​​the sample solution to that of the standard solution. Measurement conditions Detector: UV-visible spectrophotometer Measurement wavelength: 230nm Column: A stainless steel tube having an inner diameter of 21 mm and a length of 150 mm was packed with 5 μm octadecylsilanized silica gel for liquid chromatography. Column temperature: constant temperature around 40°C Mobile phase: Approximately 0.68 g of sodium acetate and 0.91 g of acetic acid were dissolved in 750 mL of ultrapure water, and then 250 mL of acetonitrile was added and mixed. ·HPLC / UV conditions Device: UltiMate 3000 system (Thermo Fisher Scientific) Column: L column 2 ODS 5 μm 2.1 × 150 mm (Chemicals Evaluation and Research Institute, Japan) Column temperature: 40℃ Mobile phase: 20 mM ammonium acetate, 25% acetonitrile buffer Analysis time: 10 minutes Detector: DAD (Diode Array Detector) Detection wavelength: 230 nm Flow rate: 0.3 mL / min (isocratic elution) Injection volume: 10μL

[0210] <Weight average molecular weight of styrene-maleic acid copolymer> In this specification, the weight average molecular weight of the styrene-maleic acid copolymer was measured under the following conditions, and the weight average molecular weight was calculated in terms of polystyrene. (1) Reagents Ultrapure water: Milli-Q ultrapure water production system, manufactured by Millipore Dimethylformamide (DMF): Special grade, manufactured by Kanto Chemical Co., Ltd. Lithium bromide monohydrate (LiBr): Special grade, manufactured by Kanto Chemical Co., Ltd. Phosphoric acid: Special grade, manufactured by Sigma-Aldrich (2) Sample pretreatment method Approximately 50 mg of sample was precisely weighed, 0.5 mL of ultrapure water was added, and 10 mL of the mobile phase described below was added to dissolve the solution, which was then filtered to prepare a sample solution. (3) Measurement Using the sample solution and the standard solution, gel permeation chromatography (GPC) measurement was carried out under the following conditions to determine the weight average molecular weight in terms of polystyrene. ·Flow rate: 1mL / min Mobile phase: 60 mM phosphoric acid, 50 mM LiBr in DMF Column: TSKgel α (Alpha) column (Tosoh Corporation) Detector: RI (Differential Refractive Index Detector)

[0211] <Quantitative determination of styrene-maleic acid copolymer in modified regenerated collagen fibers> In this specification, the amount of styrene-maleic acid copolymer in the modified regenerated collagen fiber B2 obtained in Production Example 3 was determined by the following method. (1) Reagents 1 mol / L sodium hydroxide solution: for volumetric analysis, manufactured by Fujifilm Wako Pure Chemical Industries, Ltd. Ultrapure water: Milli-Q ultrapure water production system, manufactured by Millipore Dimethylformamide (DMF): Special grade, manufactured by Kanto Chemical Co., Ltd. Lithium bromide monohydrate (LiBr): Special grade, manufactured by Kanto Chemical Co., Ltd. Phosphoric acid: Special grade, manufactured by Sigma-Aldrich (2) Sample solution The sample (modified regenerated collagen fiber B2) was conditioned at 20°C and 65% relative humidity for 24 hours, then finely chopped, and approximately 50 mg was precisely weighed out. 10 mL of a 1 mol / L aqueous solution of sodium hydroxide was added, and the mixture was heated and dissolved at 50°C for 3 hours. The pH of the solution was adjusted to 4.7-5.3, and the freeze-dried sample was diluted with 0.5 mL of ultrapure water and 9.5 mL of the mobile phase described below. The diluted solution was then filtered to prepare the sample solution. (3) Preparation of calibration curve solution Separately, styrene-maleic acid copolymer was dissolved in the mobile phase described below to prepare a non-dissociated styrene-maleic acid copolymer with a concentration of 0.25 to 5.0 mg / mL, which was used as a standard solution for drawing a calibration curve. (4) Measurement Using the sample solution and the standard solution, gel permeation chromatography (GPC) measurements were performed under the following conditions to determine the peak areas of the sample solution and the standard solution. A calibration curve was also created based on the peak area of ​​the standard solution. ·Flow rate: 0.8mL / min Mobile phase: 60 mM phosphoric acid, 50 mM LiBr in DMF Column: TSKgel α (Alpha) column (Tosoh Corporation) Detector: UV-visible spectroscopic detector ·Measurement wavelength: 267nm (5) Calculation of the amount of styrene-maleic acid copolymer The amount of styrene-maleic acid copolymer per fiber mass was calculated using a calibration curve created based on the peak area derived from the styrene-maleic acid copolymer contained in the modified regenerated collagen fiber.

[0212] <Quantitative determination of aluminum in modified regenerated collagen fibers> In this specification, the quantitative determination of aluminum in the modified regenerated collagen fibers was carried out by the following method. (1) Reagents Sulfuric acid: for precision analysis, manufactured by Fujifilm Wako Pure Chemical Industries, Ltd. Hydrochloric acid: for metal analysis, manufactured by Kanto Chemical Co., Ltd. Sodium carbonate: Special grade, manufactured by Fujifilm Wako Pure Chemical Industries, Ltd. Boric acid: Special grade, manufactured by Fujifilm Wako Pure Chemical Industries, Ltd. Aluminum standard solution: 1000 mg / L for atomic absorption analysis, manufactured by Kanto Chemical Co., Ltd. Ultrapure water: Milli-Q ultrapure water production system, manufactured by Millipore (2) Sample pretreatment method The modified regenerated collagen fiber bundle was hung in a dryer (SOFW-450SB, AS ONE Corporation) set to 60°C, a 250g weight was attached to the bottom end of the fiber bundle, and the fiber was dried for 1 hour under tension. The fiber was then removed from the dryer and conditioned at 20°C and 65% relative humidity for 24 hours. 0.1 g of sample (modified regenerated collagen fiber) was precisely weighed into a platinum crucible and heated until no more white smoke was emitted. After adding several drops of sulfuric acid, the mixture was heated again until no more white smoke was emitted and thoroughly incinerated in an electric furnace at 550°C. 1 g of an alkaline flux (sodium carbonate:boric acid = 1:0.4) was then added and the mixture was melted in an electric furnace at 950°C. A watch glass was placed over the sample, and 5 mL of ultrapure water and hydrochloric acid (6 mol / L) were added. The mixture was heated and dissolved on a hot plate at 70-80°C. After cooling, the solution was adjusted to a constant volume of 50 mL with ultrapure water and used as the measurement solution. (3) Preparation of calibration curve solution Using an aluminum standard solution (1000 mg / L), calibration curve solutions of 0.1 to 20 mg / L were prepared. An alkali flux and hydrochloric acid were added to each solution so that the concentrations were the same as those of the measurement solutions. (4) Measurement Using the prepared measurement solution, each element was measured under the following conditions using an ICP emission spectrometer. Analytical equipment: iCAP6500Duo (Thermo Fisher Scientific) ·Wavelength: Al 396.152nm RF power: 1150W Coolant gas flow rate: 12L / min Nebulizer flow rate: 0.70L / min Auxiliary gas: 0.5L / min Pump flow rate: 50 rpm

[0213] Manufacturing Example 1 (Manufacturing of regenerated collagen fiber C0) Cowhide split hide was solubilized with alkali according to standard methods to prepare a spinning dope, which was then extruded from a spinning nozzle into a coagulation bath to produce regenerated collagen fibers. The regenerated collagen fibers were immersed in 30 parts by mass of an aqueous solution containing 5.0% by mass of aluminum sulfate 14-18 hydrate, 0.65% by mass of citric acid monohydrate, and 1.3% by mass of sodium hydroxide (component (C))) at 30°C with circulation, with the dry mass being the fiber mass after conditioning at 20°C and 65% relative humidity for 24 hours. A 5% aqueous solution of sodium hydroxide was then added in portions over approximately 1 to 5 hours to adjust the final pH of the solution to 4.5 to 5.0 after 5 hours. The fibers were then left in the solution for another 3 hours and thoroughly washed with water to obtain regenerated collagen fibers C0.

[0214] Production Example 2 (Production of Modified Regenerated Collagen Fiber B1) The regenerated collagen fiber C0 obtained in Production Example 1 was treated according to the following procedure to obtain modified regenerated collagen fiber B1. (Step 1) Ten 30 cm long fiber bundles (amount that would have a mass of 1.5 g when dried at 60°C for 1 hour and then left at 20°C and 65% RH for 12 hours) were prepared from regenerated collagen fiber C0 for each example and comparative example. (Step 2) Component (B1), benzoic acid (Wako Special Grade Reagent, manufactured by Fujifilm Wako Pure Chemical Industries, Ltd., molecular weight: 122), was dissolved in water, and the pH was adjusted to 6.0 with a pH adjuster (sodium hydroxide) to prepare a fiber treatment agent containing 25.4% by mass of benzoic acid. The fiber bundles were immersed in a volume of fiber treatment agent such that the bath ratio (mass of fiber bundle after drying in step 1: mass of fiber treatment agent) was 1:30, using a separate container for each bundle, and the opening of each container was sealed. (Step 3) The container was immersed in a water bath (TBS221FA, Toyo Seisakusho Co., Ltd.) set at 40°C and left to stand for 5 minutes, and after the liquid temperature in the container was raised to 40°C, the container was removed from the water bath. (Step 4) The container containing the fiber bundle was placed on a stirring rotor (VMR-5R, AS ONE Corporation) installed in a dryer (SOFW-450SB, AS ONE Corporation) set at 40°C, and the container was rotated at a rotation speed of 80 rpm while being heated and stirred for 3 hours. (Step 5) The container containing the fiber bundle was removed from the dryer and returned to room temperature, after which the fiber bundle was taken out of the container, rinsed with running tap water at 30°C for 30 seconds, and the flow of the fibers was adjusted with a comb. (Step 6) Each fiber bundle was hung in a dryer set at 60°C, and a 250g weight was attached to the bottom end of each fiber bundle, followed by drying for 1 hour with tension applied to the entire fiber. (Step 7) The fiber bundle was removed from the dryer, allowed to cool to room temperature, and the weight was removed.

[0215] The content of benzoic acid in the modified regenerated collagen fiber B1 produced in Production Example 2 above was 27.3 mass % as benzoic acid, and the content of aluminum was 5.7 mass %.

[0216] Production Example 3 (Production of Modified Regenerated Collagen Fiber B2) The regenerated collagen fiber C0 obtained in Production Example 1 was treated according to the following procedure to obtain modified regenerated collagen fiber B2. (Step 1) Ten 30 cm long fiber bundles (amount that would have a mass of 1.5 g when dried at 60°C for 1 hour and then left at 20°C and 65% RH for 12 hours) were prepared from regenerated collagen fiber C0 for each example. First, using the B2a agent shown in Table 1, the following (Procedure 2) to (Procedure 5) were carried out. Agents B2a and B2b shown in Table 1 were prepared by blending and mixing the components listed in Table 1 using styrene-maleic acid copolymer (XIRAN1000HNa, manufactured by Polyscope, weight average molecular weight (Mw): 9195, acid value: 475 mg KOH / g, styrene / maleic acid molar ratio: 1 / 1) as component (B2). (Step 2) The fiber bundles prepared in (Procedure 1) were immersed in an amount of B2a agent such that the bath ratio (mass of fiber bundle after drying in Procedure 1: mass of B2a agent) was 1:30, using a separate container for each bundle, and the opening of each container was sealed. (Step 3) The container was immersed in a water bath (TBS221FA, Toyo Seisakusho Co., Ltd.) set at 40°C and left to stand for 5 minutes, and after the liquid temperature in the container was raised to 40°C, the container was removed from the water bath. (Step 4) The container containing the fiber bundle was placed on a stirring rotor (VMR-5R, AS ONE Corporation) installed in a dryer (SOFW-450SB, AS ONE Corporation) set at 40°C, and the container was rotated at a rotation speed of 80 rpm while being heated and stirred for 6 hours. (Step 5) The container containing the fiber bundle was removed from the dryer and returned to room temperature, after which the fiber bundle was taken out of the container, rinsed with running tap water at 30°C for 30 seconds, and the fiber flow was adjusted with a comb. (Step 6) The fiber bundle obtained in (Procedure 5) was subjected to (Procedure 2) to (Procedure 5) again, using the agent B2b shown in Table 1 instead of the agent B2a. However, the heating and stirring time in (Procedure 4) was set to 1 hour. (Step 7) The fiber bundles obtained in (Step 6) were hung one by one in a dryer set at 60°C, and a 250 g weight was attached to the bottom end of each fiber bundle, followed by drying for 1 hour with tension applied to the entire fiber. (Step 8) The fiber bundle was removed from the dryer, allowed to cool to room temperature, and the weight was removed.

[0217] [Table 1]

[0218] The blending amounts (mass %) shown in Table 1 are all amounts of active ingredients. The modified regenerated collagen fiber B2 produced in Production Example 3 above had a styrene-maleic acid copolymer content of 31.4 mass % and an aluminum content of 5.5 mass %.

[0219] Examples 1 to 3 and Comparative Example 1 (Preparation of dye composition for regenerated collagen fibers) The components shown in "First Agent" in Table 2 were blended in the blending ratios shown in Table 2 and mixed until uniform to prepare the first agent. Similarly, the components shown in "Second Agent" in Table 2 were blended in the blending ratios shown in Table 2 and mixed until uniform to prepare a second agent. Next, the first agent and the second agent were mixed in the mass ratio shown in Table 2 to prepare a dye composition for regenerated collagen fibers.

[0220] Examples 4 to 8 and Comparative Examples 2 to 5 (Evaluation of dye compositions for regenerated collagen fibers) The dyeing properties and fastness of the dye compositions obtained by the above method were evaluated by the following methods. The results are shown in Table 2.

[0221] <Dyeability (color difference before and after dyeing ΔE * ab)> A fiber bundle having a length of 10 cm and a mass of 1 g was prepared using the modified regenerated collagen fibers shown in Table 2. The fiber bundle was washed with plain shampoo having the following composition, then rinsed with warm water at 40°C, and thoroughly dried with a dryer. The hue (L0 * ,a0 * ,b0 * ) was measured using a color difference meter (CR-400, Konica Minolta, Inc.). * ,a0 * ,b0 * The values ​​were measured at six points per fiber bundle and the average value was calculated. Next, 2 g of a dye composition prepared by mixing the first and second agents shown in Table 2 in the ratios shown in Table 2 was applied to the fiber bundle, and the fiber bundle was placed in a glass petri dish, the opening of which was covered with aluminum foil, and the fiber bundle was left floating in a water bath (TBS221FA, Toyo Seisakusho Co., Ltd.) set to 30°C for 30 minutes. After leaving the fiber bundle for 30 minutes, the fiber bundle was rinsed with 40°C warm water for 30 seconds to wash away the dye composition, and the fiber bundle was lathered with a plain shampoo of the following composition for 15 seconds and then rinsed with 40°C warm water for 15 seconds, this operation being repeated twice. Next, a plain conditioner of the following composition was applied for 15 seconds, followed by rinsing with 40°C warm water for 15 seconds, and the fiber bundle was thoroughly dried with cold air from a dryer. The dried fiber bundle (dyed fiber bundle) was measured for hue (L1 * ,a1 * ,b1 * ) was measured. The color difference ΔE before and after dyeing of the fiber bundle is calculated using the following formula: * ab1 was calculated and is shown in Table 2. ΔE * A larger ab1 value means higher staining.

[0222] ΔE * ab1=〔(L1 * -L0 * ) 2 +(a1 * -a0 * ) 2 +(b1 * -b0 * ) 2 〕 1 / 2

[0223] (Plain shampoo composition) Ingredients (mass %) Polyoxyethylene (2) lauryl ether sodium sulfate (*1) 15.5 Lauric acid diethanolamide (*2) 1.5 edetic acid tetrasodium salt 0.3 Sodium benzoate 1.43 Refined water residue Total 100.0 *1: 57.4% by mass of Emar 227 (manufactured by Kao Corporation, active ingredient 27% by mass) *2: Aminone L-02 (Kao Corporation)

[0224] (Plain conditioner composition) Ingredients (mass %) Trimethylstearylammonium chloride (*1) 1.01 Distearyldimethylammonium chloride (*2) 2.0 Propylene glycol 5.0 Cetyl alcohol (*3) 2.0 Isopropyl alcohol 0.4 Methyl parahydroxybenzoate(*4) 0.1 Refined water residue Total 100.0 *1: 3.6% by mass of Kotamin 86W (manufactured by Kao Corporation, active ingredient 28% by mass) *2: 2.7% by mass of Kotamin D86P (manufactured by Kao Corporation, active ingredient 75% by mass) *3: Kalcol 6870 (Kao Corporation) *4: Mekkinsu M (manufactured by Ueno Pharmaceutical Co., Ltd.)

[0225] <Fastness (resistance to fading after washing)> The dyed fiber bundle obtained in the above-mentioned "dyeability" evaluation was used as the "fiber bundle before washing." The fiber bundle before washing was immersed in a container containing 15 g of a solution prepared by diluting the plain shampoo 10 times with purified water, and the container containing the fiber bundle was placed on a stirring rotor (VMR-5R, AS ONE Corporation) installed in a dryer (SOFW-450SB, AS ONE Corporation) set to 40°C. The container was rotated at a rotation speed of 80 rpm, and heated and stirred for 90 minutes. The container containing the fiber bundle was removed from the dryer and returned to room temperature. The fiber bundle was then removed from the container, rinsed with running water (tap water) at 40°C for 30 seconds, and thoroughly dried with cold air from a dryer. The hue (L2 * ,a2 * ,b2 *) was measured. The color difference ΔE before and after cleaning of the fiber bundle is calculated using the following formula: * ab2 was calculated and shown in Table 2. ΔE * The smaller the value of ab2, the smaller the color change due to washing.

[0226] ΔE * ab2=〔(L1 * -L2 * ) 2 +(a1 * -a2 * ) 2 +(b1 * -b2 * ) 2 〕 1 / 2

[0227] Dyeability ΔE before washing * When ab1 is small, the color difference ΔE before and after washing * It was found that ab2 was measured to be small. Therefore, in the present invention, in order to evaluate robustness more accurately, we decided to evaluate robustness using D obtained by the following formula as an index. The smaller the value of D, the higher the robustness.

[0228] D=(ΔE * ab2 / ΔE * ab1) × 100

[0229] The blending amounts (mass %) shown in Table 2 are all amounts of active ingredients.

[0230] [Table 2]

[0231] Table 2 shows that the dye composition of the present invention has better fastness to specific modified regenerated collagen fibers than the dye composition of Comparative Example 1, which uses an oxidative dye intermediate that does not contain either component (A1) or (A2).

[0232] The effects of the present invention can also be achieved by using the modified regenerated collagen fibers shown in Formulation Example 1. Prescription example 1 The regenerated collagen fiber C0 obtained in Production Example 1 was treated in the same manner as in Production Example 3, using XIRAN3000HNa (weight average molecular weight (Mw): 13803, acid value: 285 mg KOH / g, styrene / maleic acid molar ratio: 3 / 1, manufactured by Polyscope) instead of XIRAN1000HNa (manufactured by Polyscope), to obtain modified regenerated collagen fiber X3. Next, the modified regenerated collagen fibers X3 are treated using the treatment composition shown in Table 1 in the same procedure as shown in (Fiber treatment).

[0233] The effects of the present invention can also be achieved by using the dye compositions shown in Formulation Examples 2 and 3.

[0234] [Table 3] [Industrial Applicability]

[0235] According to the present invention, a dye composition for regenerated collagen fibers, which uses a dye and has excellent fastness for specific modified regenerated collagen fibers, can be provided.

Claims

1. A dye composition for regenerated collagen fibers, which comprises a mixture of at least a first agent and a second agent, the first agent contains an oxidation dye intermediate (A) containing one or more selected from the group consisting of the following components (A1) and (A2), an alkali agent, and water; the second agent contains hydrogen peroxide and water, The regenerated collagen fiber comprises a modified regenerated collagen fiber containing one or more compounds (B) selected from the group consisting of the following components (B1) and (B2): Dyeing composition for regenerated collagen fibers. (A1) One or more couplers selected from the group consisting of couplers (A1-1) having a benzene ring, electron-donating groups at the 1st and 3rd positions on the benzene ring, and hydrogen atoms at the 4th and 6th positions; couplers (A1-2) having a pyridine ring, electron-donating groups at the 2nd and 6th positions on the pyridine ring, and hydrogen atoms at the 3rd and 5th positions; and couplers (A1-3) represented by the following general formula (A13): 【Chemistry 1】 (In formula (A13), R １１ is -O-(CH ２ ) ｎ R is a divalent group represented by —O— (n is a number of 2 or more and 10 or less). １２ , R １４ , R ２２ and R ２４ is an electron donating group, R １５ and R ２５ is a hydrogen atom. １３ , R １６ , R ２３ and R ２６ are each independently a hydrogen atom, an alkyl group, or an electron-donating group. (A2) One or more couplers other than the component (A1), selected from the group consisting of couplers (A2-1) having a benzene ring, electron-donating groups at the 1- and 2-positions on the benzene ring, and hydrogen atoms at two or more of the 3- to 6-positions, and couplers (A2-2) having a pyridine ring, electron-donating groups at the 2- and 3-positions on the pyridine ring, and hydrogen atoms at two or more of the 4- to 6-positions. (B1) Benzoic acid or its salt (B2) A copolymer containing a structural unit derived from an unsaturated monomer having a carboxy group and a structural unit derived from an aromatic vinyl compound, the copolymer having an acid value of 100 mgKOH / g or more and a weight average molecular weight of 1,500 or more and 15,000 or less, or a salt thereof.

2. The dye composition for regenerated collagen fibers according to claim 1 , wherein the oxidation dye intermediate (A) comprises the component (A1).

3. 3. The dye composition for regenerated collagen fibers according to claim 1, wherein the component (A1) comprises one or more members selected from the group consisting of meta-aminophenol, resorcinol, meta-phenylenediamine, 2-methylresorcinol, 1-naphthol, 2,6-diaminopyridine, and 1,3-bis(2,4-diaminophenoxy)propane.

4. 4. The dye composition for regenerated collagen fibers according to claim 3, wherein the component (A1) comprises one or more members selected from the group consisting of meta-aminophenol, resorcinol, 2-methylresorcinol, and 1-naphthol.

5. the oxidation dye intermediate (A) further contains a precursor as component (A3), 3. The dye composition for regenerated collagen fibers according to claim 1, wherein the precursor comprises one or more members selected from the group consisting of toluene-2,5-diamine, paraaminophenol, 4-amino-metacresol, 1-hydroxyethyl-4,5-diaminopyrazole, and salts thereof.

6. 3. The dye composition for regenerated collagen fibers according to claim 1, wherein the component (B2) comprises a styrene-maleic acid copolymer.

7. A method for dyeing regenerated collagen fibers, comprising: The method includes the following steps (I) and (II) in this order: The regenerated collagen fiber comprises a modified regenerated collagen fiber containing one or more compounds (B) selected from the group consisting of the following components (B1) and (B2): Method for dyeing regenerated collagen fibers. Process (I) A step of mixing at least the first agent and the second agent to prepare a dye composition for regenerated collagen fibers. Here, the first agent contains an oxidation dye intermediate (A) containing one or more selected from the group consisting of the following components (A1) and (A2), an alkaline agent, and water, and the second agent contains hydrogen peroxide and water. Process (II) applying the regenerated collagen fiber dye composition to the regenerated collagen fiber; (A1) One or more couplers selected from the group consisting of couplers (A1-1) having a benzene ring, electron-donating groups at the 1st and 3rd positions on the benzene ring, and hydrogen atoms at the 4th and 6th positions; couplers (A1-2) having a pyridine ring, electron-donating groups at the 2nd and 6th positions on the pyridine ring, and hydrogen atoms at the 3rd and 5th positions; and couplers (A1-3) represented by the following general formula (A13): 【Chemistry 2】 (In formula (A13), R １１ is -O-(CH ２ ) ｎ R is a divalent group represented by —O— (n is a number of 2 or more and 10 or less). １２ , R １４ , R ２２ and R ２４ is an electron donating group, R １５ and R ２５ is a hydrogen atom. １３ , R １６ , R ２３ and R ２６ are each independently a hydrogen atom, an alkyl group, or an electron-donating group. (A2) One or more couplers other than the component (A1), selected from the group consisting of couplers (A2-1) having a benzene ring, electron-donating groups at the 1- and 2-positions on the benzene ring, and hydrogen atoms at two or more of the 3- to 6-positions, and couplers (A2-2) having a pyridine ring, electron-donating groups at the 2- and 3-positions on the pyridine ring, and hydrogen atoms at two or more of the 4- to 6-positions. (B1) Benzoic acid or its salt (B2) A copolymer containing a structural unit derived from an unsaturated monomer having a carboxy group and a structural unit derived from an aromatic vinyl compound, the copolymer having an acid value of 100 mgKOH / g or more and a weight average molecular weight of 1,500 or more and 15,000 or less, or a salt thereof.

8. A colored modified regenerated collagen fiber containing the following component (A0) and component (B): (A0) A reaction product of an oxidation dye intermediate (A) containing at least one selected from the group consisting of the following components (A1) and (A2): (A1) One or more couplers selected from the group consisting of couplers (A1-1) having a benzene ring, electron-donating groups at the 1st and 3rd positions on the benzene ring, and hydrogen atoms at the 4th and 6th positions; couplers (A1-2) having a pyridine ring, electron-donating groups at the 2nd and 6th positions on the pyridine ring, and hydrogen atoms at the 3rd and 5th positions; and couplers (A1-3) represented by the following general formula (A13): 【Transformation 3】 (In formula (A13), R １１ is -O-(CH ２ ) ｎ R is a divalent group represented by —O— (n is a number of 2 or more and 10 or less). １２ , R １４ , R ２２ and R ２４ is an electron donating group, R １５ and R ２５ is a hydrogen atom. １３ , R １６ , R ２３ and R ２６ are each independently a hydrogen atom, an alkyl group, or an electron-donating group. (A2) One or more couplers other than the component (A1), selected from the group consisting of couplers (A2-1) having a benzene ring, electron-donating groups at the 1- and 2-positions on the benzene ring, and hydrogen atoms at two or more of the 3- to 6-positions, and couplers (A2-2) having a pyridine ring, electron-donating groups at the 2- and 3-positions on the pyridine ring, and hydrogen atoms at two or more of the 4- to 6-positions. (B) One or more compounds selected from the group consisting of the following components (B1) and (B2): (B1) Benzoic acid or its salt (B2) A copolymer containing a structural unit derived from an unsaturated monomer having a carboxy group and a structural unit derived from an aromatic vinyl compound, the copolymer having an acid value of 100 mgKOH / g or more and a weight average molecular weight of 1,500 or more and 15,000 or less, or a salt thereof.

9. A headwear product comprising the colored modified regenerated collagen fiber according to claim 8.

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