WO2016047665A1 - Hair dye and hair dyeing method - Google Patents
Hair dye and hair dyeing method Download PDFInfo
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- WO2016047665A1 WO2016047665A1 PCT/JP2015/076872 JP2015076872W WO2016047665A1 WO 2016047665 A1 WO2016047665 A1 WO 2016047665A1 JP 2015076872 W JP2015076872 W JP 2015076872W WO 2016047665 A1 WO2016047665 A1 WO 2016047665A1
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- 0 *C1[C@](O)OC(*)[C@]2(*)C1C2 Chemical compound *C1[C@](O)OC(*)[C@]2(*)C1C2 0.000 description 3
Classifications
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/96—Cosmetics or similar toiletry preparations characterised by the composition containing materials, or derivatives thereof of undetermined constitution
- A61K8/97—Cosmetics or similar toiletry preparations characterised by the composition containing materials, or derivatives thereof of undetermined constitution from algae, fungi, lichens or plants; from derivatives thereof
- A61K8/9783—Angiosperms [Magnoliophyta]
- A61K8/9789—Magnoliopsida [dicotyledons]
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/19—Cosmetics or similar toiletry preparations characterised by the composition containing inorganic ingredients
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/19—Cosmetics or similar toiletry preparations characterised by the composition containing inorganic ingredients
- A61K8/23—Sulfur; Selenium; Tellurium; Compounds thereof
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/33—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
- A61K8/34—Alcohols
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/33—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
- A61K8/35—Ketones, e.g. benzophenone
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/33—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
- A61K8/36—Carboxylic acids; Salts or anhydrides thereof
- A61K8/368—Carboxylic acids; Salts or anhydrides thereof with carboxyl groups directly bound to carbon atoms of aromatic rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/60—Sugars; Derivatives thereof
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/96—Cosmetics or similar toiletry preparations characterised by the composition containing materials, or derivatives thereof of undetermined constitution
- A61K8/97—Cosmetics or similar toiletry preparations characterised by the composition containing materials, or derivatives thereof of undetermined constitution from algae, fungi, lichens or plants; from derivatives thereof
- A61K8/9783—Angiosperms [Magnoliophyta]
- A61K8/9794—Liliopsida [monocotyledons]
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q5/00—Preparations for care of the hair
- A61Q5/10—Preparations for permanently dyeing the hair
Definitions
- the present invention relates to a hair dye and a hair dyeing method having good hair dyeing properties and little skin coloring.
- Oxidative dyes are mainly composed of paraphenylenediamines and paraaminophenols that are oxidized by hydrogen peroxide and become active reaction intermediates. The activated reaction intermediate then reacts with the dye coupler molecule in the hair and turns into a shampoo resistant dye.
- Patent Document 1 discloses a two-component hair dye composition comprising a first agent and a second agent, wherein the first agent is selected from the group consisting of (i) gallic acid and its derivatives. And / or (ii) one or more selected from the group consisting of salicylic acid and derivatives thereof, the second agent comprises an iron salt, and at least one of the first agent and the second agent.
- compositions containing urea are described.
- Patent Document 2 includes (a) a first agent that contains a substance that reacts with iron and develops color, an ultraviolet absorber having a 2-hydroxybenzophenone skeleton, and (b) a second agent that contains an iron salt.
- a hair dye containing in combination is described.
- Patent Document 3 discloses (A) at least one phenolic compound selected from gallic acid, tannic acid, salicylic acid and derivatives thereof, pyrogallol, catechol and hematein, and a surfactant as a cleaning active ingredient.
- a hair dye composition comprising a shampoo solution containing a first agent and a rinse solution containing (B) a polyvalent metal salt and a cationic surfactant as a second agent is described.
- Patent Document 4 discloses a hair treatment agent comprising a first agent containing an alkaline agent and a second agent containing an oxidizing agent, wherein the hair contains polyoxyalkylene methyl glucoside. Hair treatment agents for depigmenting agents or oxidative hair dyes are described. Further, Patent Document 5 describes a composition for compounding a stain remover containing alcohols, and polyoxypropylene methyl glucoside is described as an example of alcohols.
- JP 2008-273869 A JP2011-126845A Japanese Patent Laid-Open No. 4-164017 JP 2011-57627 A JP 2001-226241 A
- Oxidative dyes can cause hair damage and contact dermatitis.
- the oxidation dye since the oxidation dye remains in the human body for a long time, it may become a mutagenic or carcinogenic substance.
- Ionic dyes sometimes called semi-permanent dyes, do not damage hair, but can cause skin coloration during hair dyeing.
- ionic dyes may flow down from the hair after 4 to 10 shampoo operations.
- Temporary dyes do not damage the hair and can wash off the skin coloring, but only one shampoo operation is possible. May flow out of the hair.
- Patent Documents 1 to 3 describe metal hair dyes using iron salts, but do not describe skin coloring.
- it aims at preventing the damage of hair and giving the excellent fingering property and gloss to the hair after treatment, and it is limited to an oxidation hair dye as a hair dye.
- Patent Document 5 relates to a composition for compounding a stain remover, not a hair dye. That is, the composition of patent document 5 is for removing the oxidation dye or ionic dye colored on the skin, and does not prevent skin coloring of the hair dye.
- hair dyes there is a problem that skin coloring tends to occur when trying to improve hair coloring, and hair coloring becomes low when trying to suppress skin coloring.
- This invention made it the subject which should be solved to provide the hair dye and hair dyeing method with favorable hair dyeing property and little skin coloring.
- the present inventors have found that the first agent containing a substance that develops color by reacting with iron and the hair dye containing the second agent containing an iron salt, all of the first agent. It has been found that the above-mentioned problems can be solved by blending methyl glucoside having a hydrophilic group of 0.1% by mass to 12% by mass with respect to the mass into the first agent, and the present invention has been completed.
- X 1 to X 4 each independently represent a single bond or a hydrophilic group, provided that at least one of X 1 to X 4 represents a hydrophilic group.
- the hair dye according to (1), wherein the hydrophilic group is a polyoxyalkylene group.
- the hair dye according to (1) or (2), wherein the compound represented by the formula 1 is a compound represented by the following formula 1A.
- each A independently represents an ethylene group or a propylene group.
- a, b, c and d each independently represent an integer of 0 or more, provided that the sum of a, b, c and d is an integer of 5 to 30.
- the compound represented by Formula 1 is polyoxyethylene methyl glucoside having an addition mole number of polyoxyethylene of 10 to 20, or polyoxypropylene methyl glucoside having an addition mole number of polyoxypropylene of 10 to 20.
- the hair dye according to any one of (1) to (3).
- Substances that react with iron and develop color are tannic acid, salicylic acid and salicylic acid derivatives, pyrogallol, gallic acid and its derivatives, pentaploid, logwood, hematein, catechol, phthalic acid, eugenol, isoeugenol, nicotinic acid Amide, dehydroacetic acid, pyridoxine, ellagic acid, kojic acid, maltol, ferulic acid, hinokitiol, turmeric extract, curcumin, ougon extract, onion extract, quercetin, rutin, hesperetin, hesperidin, fresh coffee bean extract, caffeic acid, chlorogenic acid , Tea extract, catechin, epicatechin, shikon extract, shiso extract, shisonin, grape leaf extract, butto extract, enocyanin, lacainate, lac, cochineal, carminic acid, elderberry, red cabbage, mura Kiimo, tamarind,
- the substance that develops color by reacting with iron is a combination of tannic acid and salicylic acid or a salicylic acid derivative, or a combination of pyrogallol and gallic acid or a derivative thereof.
- the first agent includes a combination of tannic acid and salicylic acid or a salicylic acid derivative, or a combination of pyrogallol and gallic acid or a derivative thereof as a substance that develops color by reacting with iron, and is represented by Formula 1.
- the iron salt is at least one selected from the group consisting of ferrous sulfate, ferrous chloride, ferrous acetate, ferric sulfate, ferric hydrochloride and ferric acetate.
- a hair dyeing method comprising applying the hair dye according to any one of (1) to (12) to hair.
- hair dye and hair dyeing method of the present invention skin coloring can be reduced while maintaining good hair dyeing properties.
- a numerical range indicated by using “to” indicates a range including the numerical values described before and after “to” as the minimum value and the maximum value, respectively.
- the hair dye of the present invention comprises a substance that develops color by reacting with iron, and a first agent comprising 0.1% by mass to 12% by mass of the compound represented by formula 1 with respect to the total mass of the first agent; It is a two-component hair dye containing a combination of a second agent containing an iron salt.
- a first agent comprising 0.1% by mass to 12% by mass of the compound represented by formula 1 with respect to the total mass of the first agent
- It is a two-component hair dye containing a combination of a second agent containing an iron salt.
- the first agent contains 0.1% by mass to 12% by mass of the compound represented by the following formula 1 with respect to the total mass of the first agent.
- X 1 to X 4 each independently represent a single bond or a hydrophilic group, provided that at least one of X 1 to X 4 represents a hydrophilic group.
- the hydrophilic group represented by X 1 to X 4 is a divalent hydrophilic group, and the type thereof is not particularly limited, but a nonionic hydrophilic group is preferable.
- the nonionic hydrophilic group include a polyoxyalkylene group.
- the number of carbon atoms in the above alkylene is not particularly limited, but is preferably 1 to 5, more preferably 2 to 4, and particularly preferably 2 or 3.
- the polyoxyalkylene group include a polyoxyethylene group, a polyoxypropylene group, a polyoxyethylene-polyoxypropylene group, a polyoxyethylene-polyoxypropylene-oxybutylene group, and the like. Among these, a polyoxyethylene group is preferable from the viewpoint of good hair dyeability and suppression of skin coloring.
- the compound represented by the formula 1 is preferably a compound represented by the following formula 1A.
- each A independently represents an ethylene group or a propylene group.
- a, b, c and d each independently represent an integer of 0 or more.
- the added mole number of polyoxyalkylene is an integer of 5 to 30, preferably an integer of 5 to 25, and more preferably an integer of 10 to 20.
- Particularly preferred examples of the compound represented by Formula 1 include polyoxyethylene methylglucoside having a polyoxyethylene addition mole number of 10 to 20 (for example, 10 or 20), or polyoxypropylene addition mole number of 10 to Polyoxypropylene methyl glucoside that is 20 (eg 10 or 20).
- Macbiobride® MG-10E Polyoxyethylene methyl glucoside macbiobroide (registered trademark) MG-20E having an addition mole number of polyoxyethylene of 10: Polyoxyethylene methyl glucoside macbiobroide (registered trademark) MG-10P having a polyoxyethylene addition mole number of 10: Polyoxypropylene methylglucoside macbiobroide (registered trademark) MG-20P in which the number of moles of polyoxypropylene added is 10: Polyoxypropylene methylglucoside having an addition mole number of polyoxypropylene of 20.
- AO represents a random copolymer of ethylene oxide and propylene oxide
- BO represents butylene oxide
- the compound represented by Formula 1 one type of compound may be used, or two or more types of compounds may be used in combination.
- the content of the compound represented by Formula 1 is 0.1% by mass to 12% by mass with respect to the total mass of the first agent, and preferably 0.2% by mass to 10% by mass. % To 5% by mass is more preferable, and 2% to 3% by mass is most preferable.
- the total content is preferably within the above range.
- an organic compound or plant extract that develops color by reacting with iron can be used as the substance that develops color by reacting with iron used in the present invention.
- substances that develop color by reacting with iron include tannic acid, salicylic acid and salicylic acid derivatives, pyrogallol, gallic acid and its derivatives, pentaploid, logwood, hematein, catechol, phthalic acid, eugenol, isoeugenol, nicotinamide , Dehydroacetic acid, pyridoxine, ellagic acid, kojic acid, maltol, ferulic acid, hinokitiol, turmeric extract, curcumin, ougon extract, onion extract, quercetin, rutin, hesperetin, hesperidin, raw coffee bean extract, caffeic acid, chlorogenic acid, Cha extract, catechin, epicatechin, shikon extract, perilla extract, shisonin, grape leaf extract, butter extract, enocyanin,
- more preferable is at least one selected from tannic acid, salicylic acid and derivatives thereof, pyrogallol, and gallic acid and derivatives thereof.
- the substance that develops color by reacting with iron is particularly preferably a combination of tannic acid and salicylic acid or a salicylic acid derivative, or a combination of pyrogallol and gallic acid or a derivative thereof.
- Examples of derivatives of gallic acid include alkyl esters of gallic acid, and examples of alkyl esters of gallic acid include linear or branched alkyl esters having 1 to 10 carbon atoms, preferably 2 to 5 carbon atoms. Can be mentioned. For example, ethyl gallate, propyl gallate, isoamyl gallate and the like are included.
- Gallic acid or a derivative thereof may be chemically synthesized by a known method or may be isolated from a plant. What further added chemical synthesis to what was isolated from the plant may be used. Moreover, you may use the extract containing the gallic acid obtained from a plant, or its derivative (s) as it is.
- gallic acid derived from leguminous plant cod gallic acid derived from pentaploid which occurs in urchinaceae, or extracts containing them can be used.
- derivatives obtained by chemically esterifying those gallic acids can also be used.
- Salicylic acid derivatives include salicylic acid esters and salts.
- the salicylic acid salt include alkali metal salts of salicylic acid. Specific examples include sodium salicylate.
- Examples of the salicylic acid ester include methyl salicylate and ethyl salicylate.
- the substance that reacts with iron and develops color one kind of compound may be used, or two or more kinds of compounds may be used in combination.
- the content of the substance that develops color by reacting with iron is preferably 0.5% by mass to 10% by mass, and preferably 0.5% by mass to 6% by mass with respect to the total mass of the first agent. More preferred.
- the total content is preferably within the above range.
- the first agent may further contain an ultraviolet absorber having a 2-hydroxybenzophenone skeleton.
- an ultraviolet absorber having a 2-hydroxybenzophenone skeleton a compound having a 2-hydroxybenzophenone skeleton represented by the following general formula (2) can be preferably used.
- X and Y each independently represent a hydroxyl group, an alkoxy group having 1 to 16 carbon atoms, an alkyl group having 1 to 16 carbon atoms, a sulfo group, a carboxyl group, or a halogen atom.
- P is an integer of 1 to 4)
- Q represents an integer of 0 to 5)
- ultraviolet absorber having a 2-hydroxybenzophenone skeleton examples include oxybenzone-1 (2,4-dihydroxybenzophenone), oxybenzone-3 (2-hydroxy-4-methoxybenphenone), and oxybenzone-4 (2-hydroxybenzone-4).
- a compound having a ClogP of 1 or more and 7 or less is preferably used as the ultraviolet absorber having a 2-hydroxybenzophenone skeleton.
- a compound having ClogP of 1 or more and 7 or less By using a compound having ClogP of 1 or more and 7 or less, a particularly good staining effect can be achieved. The reason for this is presumed that by using a compound having a ClogP of 1 or more and 7 or less, this compound also penetrates into the hair, forms an iron chelate in the hair, and contributes to dyeing.
- LogP is a parameter representing hydrophobicity and represents a partition coefficient between water and octanol. With the recent development of computational chemistry, the value of logP can be obtained by calculation on a computer, and this value is called ClopP.
- the structure and ClogP of typical compounds among ultraviolet absorbers having a 2-hydroxybenzophenone skeleton are described below.
- the amount used in the case of using an ultraviolet absorber having a 2-hydroxybenzophenone skeleton is not particularly limited, but is preferably 0.5% by mass to 10% by mass with respect to the total mass of the first agent, and 1% by mass. More preferably, it is ⁇ 6% by mass.
- the total content is preferably within the above range.
- the first agent may further contain 0.5% by mass to 10% by mass of an ammonium salt based on the total mass of the first agent.
- ammonium salts include ammonium bicarbonate, ammonium sulfate, ammonium acetate, ammonium chloride, ammonium carbonate, ammonium nitrate, ammonium perchlorate, and the like. These may be used alone or in combination of two or more. You may use together.
- ammonium hydrogen carbonate can be used.
- the content thereof is not particularly limited, but is preferably 0.5% by mass to 10% by mass, and more preferably 1% by mass to 5% by mass.
- the total content is preferably within the above range.
- the first agent may further contain 1% by mass to 12% by mass, more preferably 1% by mass to 5% by mass, based on the total mass of the first agent.
- benzil alcohol By containing benzil alcohol, it is possible to swell the cuticle and improve the hair dyeing property.
- Benzyl alcohol can be used as a solvent.
- the first agent may further contain an antioxidant.
- an antioxidant what can be used for a normal hair dye can be used, and sulfite, bisulfite, thiosulfate, ascorbic acid, thioglycolic acid, cysteine, mercapto compound, etc. are mentioned.
- Specific examples of the antioxidant include sodium sulfite, L-ascorbic acid and its salt, thioglycolic acid and its salt, L-cysteine and its salt, and N-acetyl-L-cysteine and its salt. It is done. Among these, sodium sulfite is preferable because it not only contributes to the stabilization of the dye precursor, but also improves the hair dyeing power. Any one antioxidant may be used alone, or two or more antioxidants may be used in combination.
- the antioxidant when used, its content is not particularly limited, but it is preferably 0.5% by mass to 10% by mass and preferably 1% by mass to 6% by mass with respect to the total mass of the first agent. More preferably. When using 2 or more types of antioxidant, it is preferable that total content becomes the said range.
- a compound represented by the formula 1 which includes a combination, polyoxyethylene methyl glucoside having an addition mole number of polyoxyethylene of 10 or 20, or polyoxypropylene methyl glucoside having an addition mole number of polyoxypropylene of 10 or 20
- an oxybenzene-4, oxybenzene-3 or oxybenzene-1 as an ultraviolet absorber having a 2-hydroxybenzophenone skeleton, and 0.5 wt% to 10 wt% with respect to the total weight of the first agent
- ammonium hydrogen carbonate 1% by mass relative to the total mass of the first agent Further comprising a 12 weight percent benzyl alcohol, can be mentioned may further comprise sodium sulfite as an antioxidant.
- the second agent in the hair dye of the present invention contains an iron salt.
- the iron salt used in the present invention is not particularly limited as long as it can exhibit a hair dyeing action, but in general, ferrous sulfate, ferrous chloride, ferrous acetate, ferric sulfate, chloride Of these, ferric sulfate or ferric chloride can be used. Ferric sulfate, ferric acetate and the like can be used.
- the amount of iron salt used is not particularly limited as long as the effect of the present invention is obtained, but it is preferably 0.5 to 10% by mass, preferably 1 to 6% by mass with respect to the total mass of the second agent. .
- the second agent may further contain the antioxidant described in the first agent in addition to the iron salt. More preferably, the second agent contains at least one selected from L-ascorbic acid and salts thereof among the antioxidants. Examples of the salt of L-ascorbic acid include sodium L-ascorbate and calcium L-ascorbate. In the second agent, any one of the antioxidants may be used alone, or two or more may be used in combination. When the second agent contains an antioxidant, the content thereof is not particularly limited, but may be 0.5% by mass to 10% by mass with respect to the total mass of the second agent, and may be 1% by mass to 6%. It is more preferable to contain by mass.
- various components may be added to the first agent and / or the second agent.
- Other components include bases, surfactants, solvents, pH adjusters, wetting agents, thickeners, preservatives, fats and oils, organic acids, fragrances, metal odor masking agents, colorants, and the like. It is done.
- components that are used in ordinary cosmetics and the like within a range not impairing the object of the present invention such as hair restoration agents, anti-dandruff agents, antibacterial agents, softeners, moisturizers, active oxygen removers, anti-oxidants, Microbial agents, silicones, minerals, hydrolyzed proteins, peptides, and amino acids can be appropriately blended. The content of these other components can be appropriately set within the range where the effects of the present invention are exhibited.
- Examples of the base include higher alcohols, hydrocarbons, fatty acid esters, vegetable oils, fatty acids and the like.
- the surfactant polyoxyethylene alkyl ether, polyoxyethylene, polyoxypropylene alkyl ether, glycerin fatty acid ester, polyglycerin fatty acid ester, polyethylene glycol fatty acid ester, polyoxyethylene alkyl ether phosphoric acid and its salt, alkyl glucoside, Examples thereof include N-acyl amino acid salts, alkyl ether carboxylates, alkyl sulfates, polyoxyethylene alkyl ether sulfates, sulfonates, alkyl ammonium salts, and alkylamidopropyl betaines.
- the solvent examples include water, ethanol, isopropyl alcohol, benzyl alcohol, 1,3-butylene glycol, 2-methyl-2,4-pentanediol, glycerin, propylene glycol and the like.
- the pH adjuster ammonia, ammonium carbonate, potassium hydroxide, sodium hydroxide, monoethanolamine, isopropanolamine, hydrochloric acid and the like can be used.
- wetting agent examples include propylene glycol, glycerin, sorbitol, sodium pyrrolidone carboxylate, amino acids, vegetable oils and the like.
- thickener examples include xanthan gum, acrylic acid / alkyl methacrylate copolymer, polyethylene glycol, and hydroxyethyl cellulose. Of these, xanthan gum is preferably used as one of the preferred thickeners.
- Xanthan gum is a polysaccharide obtained by fermenting carbohydrates using Xanthomonas sp.
- the hair dye of the present invention contains a first agent and a second agent.
- the ratio of the first agent to the second agent (first agent: second agent) is preferably in the range of 1: 0.5 to 1: 2 by mass ratio, and is 1: 0.8 to 1: 1.2. The range is more preferable, and 1: 1 is more preferable.
- the pH of the first agent is preferably pH 5 to 10, more preferably pH 6 to 9.
- the pH of the second agent is preferably pH 2-6, more preferably pH 3-5.
- the dosage form of the first agent and the second agent is not particularly limited.
- it can be a cream, liquid, gel, emulsion, spray, aerosol type or the like.
- the aerosol type is preferable.
- the dosage form of the first agent and the dosage form of the second agent may be the same or different.
- the 1st agent and the 2nd agent can further contain a publicly known ingredient required for formulation which can be chosen according to the kind of each dosage form.
- an aerosol-type dosage form is manufactured by filling a pressure-resistant container with a first agent or a second agent and a compressed gas, a surfactant, a thickener and / or a liquefied gas in an anaerobic atmosphere. can do.
- the compressed gas used here is preferably nitrogen, carbonic acid, argon or the like.
- Other dosage forms can also be prepared according to known methods.
- the hair coloring method of the present invention includes applying a hair dye containing the first agent and the second agent of the present invention to hair.
- a hair dye containing the first agent and the second agent of the present invention to hair.
- the matter mentioned above is applicable as it is. Examples of hair include scalp hair.
- a method for applying to the hair there is a method in which the first agent is applied to the hair and allowed to stand for a certain period of time, and then the second agent is applied to the hair and left to stand for a certain period of time to wash away the first and second agents. Can be mentioned. Further, as another method for applying to the hair, there may be mentioned a method in which the first agent and the second agent are simultaneously applied to the hair, left for a certain period of time, and the first agent and the second agent are washed away.
- the application to hair can be performed according to a known method. Specifically, it may be applied directly to the hair or may be applied to the hair using a tool such as a hand or a brush. From the viewpoint of preventing the agent from splashing and dripping, it is more preferable to apply it to the hair using a gloved hand.
- the time for leaving the first agent and the second agent can be set as appropriate. Moreover, what is necessary is just to use a well-known method for the method of washing away the 1st agent and the 2nd agent.
- the amount of hair dye applied can be appropriately set. For example, it is preferable to apply about 30 g to 70 g of the first agent and about 30 g to 70 g of the second agent to hair having a length of about 20 cm. Further, it is more preferable to apply about 40 g to 60 g of the first agent and about 40 g to 60 g of the second agent. As an example, 50 g of the first agent and 50 g of the second agent can be applied.
- the 1st agent of the composition shown in the following Table 1 and the 2nd agent of the composition shown in the following Table 2 were manufactured by a conventional method.
- surface about each compound shows the mass% with respect to each total mass of the 1st agent or the 2nd agent.
- the appropriate amount of sodium hydroxide in Table 1 means the amount necessary to adjust to pH 7.
- the hair bundle that was dyed was measured with a CR200 color difference meter manufactured by Minolta, and evaluated based on the following criteria from the ⁇ L value with the original white hair before dyeing.
- the ⁇ L value is the difference between values measured with a color difference meter for the hair bundle before dyeing and the hair bundle after dyeing.
- the first agent of Examples and Comparative Examples was thinly applied in a circular area with a diameter of 1 cm on the inner side of the forearm of the paneler, allowed to stand for 20 minutes, then the second agent was applied again, allowed to stand for 10 minutes, and then rinsed with warm water. . Furthermore, after lightly rubbing with a finger for 1 minute using a shampoo and washing away with warm water, the degree of dyeing on the skin was evaluated according to the following criteria. A: There is almost no background dirt B: There is little background dirt C: There is background dirt
- the hair bundle dyed by the above-mentioned hair dyeing method is measured with a CR200 type color difference meter manufactured by Minolta, and the color difference ( ⁇ E value). From the evaluation, the following criteria were used.
- the ⁇ E value is a difference between values measured with a color difference meter between a product stored at 4 ° C. and a product aged at 50 ° C. for one month. A: ⁇ E ⁇ 2 (mostly no difference is visible) B: 2 ⁇ E ⁇ 4 (a slight difference can be visually observed) C: 4 ⁇ ⁇ E (a difference can be visually confirmed)
- the hair dye and hair dyeing method of the present invention can be used as a hair dye excellent in safety, hair dyeability and storage stability, and having little skin coloring.
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- Cosmetics (AREA)
Abstract
The purpose of the present invention is to provide a hair dye, which has good hair dyeing properties and minimizes the coloring of skin, and a hair dyeing method. The present invention provides a hair dye containing: a first agent that contains a substance that provides coloring by reacting with iron, and a compound represented by formula 1 comprising 0.1 mass% to 12 mass% of the total mass of the first agent; and a second agent that contains an iron salt. In the formula, X1 to X4 each independently represent a single bond or a hydrophilic group, with at least one of X1 to X4 representing a hydrophilic group.
Description
本発明は、染毛性が良くかつ皮膚着色の少ない染毛剤及び染毛方法に関する。
The present invention relates to a hair dye and a hair dyeing method having good hair dyeing properties and little skin coloring.
染毛剤は、一般的に、酸化染料、イオン染料、一時染料、及びその他の染料の4種類に分けられる。
現在最も広く用いられている酸化染料は、永久染料と呼ばれることもある。酸化染料は、過酸化水素によって酸化されて活性な反応中間体となるパラフェニレンジアミン類やパラアミノフェノール類を主原料として構成されている。活性化された反応中間体はその後に毛髪内で染料カップラー分子と反応し、耐シャンプー性の染料に変化する。 Hair dyes are generally divided into four types: oxidation dyes, ionic dyes, temporary dyes, and other dyes.
The most widely used oxidation dyes at present are sometimes called permanent dyes. Oxidative dyes are mainly composed of paraphenylenediamines and paraaminophenols that are oxidized by hydrogen peroxide and become active reaction intermediates. The activated reaction intermediate then reacts with the dye coupler molecule in the hair and turns into a shampoo resistant dye.
現在最も広く用いられている酸化染料は、永久染料と呼ばれることもある。酸化染料は、過酸化水素によって酸化されて活性な反応中間体となるパラフェニレンジアミン類やパラアミノフェノール類を主原料として構成されている。活性化された反応中間体はその後に毛髪内で染料カップラー分子と反応し、耐シャンプー性の染料に変化する。 Hair dyes are generally divided into four types: oxidation dyes, ionic dyes, temporary dyes, and other dyes.
The most widely used oxidation dyes at present are sometimes called permanent dyes. Oxidative dyes are mainly composed of paraphenylenediamines and paraaminophenols that are oxidized by hydrogen peroxide and become active reaction intermediates. The activated reaction intermediate then reacts with the dye coupler molecule in the hair and turns into a shampoo resistant dye.
上記のその他の染料としては、鉄塩を利用した金属染毛剤(非酸化型染毛剤)が提案されている。例えば、特許文献1には、第1剤及び第2剤からなる二剤式染毛剤組成物であって、第1剤が、(i)没食子酸及びその誘導体からなる群から選ばれる1以上、及び/又は、(ii)サリチル酸及びその誘導体からなる群より選ばれる1以上を含んでなり、第2剤が、鉄塩を含んでなり、かつ、第1剤及び第2剤のうち少なくとも一方が、尿素を含んでいる組成物が記載されている。特許文献2には、(a)鉄と反応して発色する物質と、2-ヒドロキシベンゾフェノン骨格を有する紫外線吸収剤とを含有する第1剤、及び(b)鉄塩を含有する第2剤を組み合わせて含む染毛剤が記載されている。さらに特許文献3には、(A)没食子酸、タンニン酸、サリチル酸及びこれらの誘導体、ピロガロール、カテコール並びにヘマテインの中から選ばれた少なくとも1種のフェノール系化合物と、洗浄活性成分としての界面活性剤とを含有するシャンプー液を第一剤とし、(B)多価金属塩と、カチオン系界面活性剤とを含有するリンス液を第二剤として成る染毛剤組成物が記載されている。
As other dyes described above, metal hair dyes (non-oxidative hair dyes) using iron salts have been proposed. For example, Patent Document 1 discloses a two-component hair dye composition comprising a first agent and a second agent, wherein the first agent is selected from the group consisting of (i) gallic acid and its derivatives. And / or (ii) one or more selected from the group consisting of salicylic acid and derivatives thereof, the second agent comprises an iron salt, and at least one of the first agent and the second agent However, compositions containing urea are described. Patent Document 2 includes (a) a first agent that contains a substance that reacts with iron and develops color, an ultraviolet absorber having a 2-hydroxybenzophenone skeleton, and (b) a second agent that contains an iron salt. A hair dye containing in combination is described. Further, Patent Document 3 discloses (A) at least one phenolic compound selected from gallic acid, tannic acid, salicylic acid and derivatives thereof, pyrogallol, catechol and hematein, and a surfactant as a cleaning active ingredient. A hair dye composition comprising a shampoo solution containing a first agent and a rinse solution containing (B) a polyvalent metal salt and a cationic surfactant as a second agent is described.
一方、特許文献4には、アルカリ剤を含有する第1剤と、酸化剤を含有する第2剤とからなる毛髪処理剤であって、ポリオキシアルキレンメチルグルコシドを含有することを特徴とする毛髪脱色剤用又は酸化染毛剤用の毛髪処理剤が記載されている。また、特許文献5には、アルコール類を含有することを特徴とするステインリムーバー配合用組成物が記載されており、アルコール類の一例として、ポリオキシプロピレンメチルグルコシドが記載されている。
On the other hand, Patent Document 4 discloses a hair treatment agent comprising a first agent containing an alkaline agent and a second agent containing an oxidizing agent, wherein the hair contains polyoxyalkylene methyl glucoside. Hair treatment agents for depigmenting agents or oxidative hair dyes are described. Further, Patent Document 5 describes a composition for compounding a stain remover containing alcohols, and polyoxypropylene methyl glucoside is described as an example of alcohols.
酸化染料は、毛髪の損傷や接触性皮膚炎を引き起こすことがある。また、酸化染料は、長期にわたり人体に残留するため、変異原性または発ガン性物質になる可能性がある。イオン染料は半永久染料と呼ばれることもあり、毛髪を損傷させることはないが、染毛の際、皮膚着色を引き起こす可能性がある。その他、イオン染料は、4~10回のシャンプー操作で毛髪から流れ落ちてしまうことがあり、一時染料は、毛髪を損傷させることもなく、皮膚着色も洗い流しが可能であるが、1回のシャンプー操作で毛髪から流れ落ちてしまうことがある。
Oxidative dyes can cause hair damage and contact dermatitis. In addition, since the oxidation dye remains in the human body for a long time, it may become a mutagenic or carcinogenic substance. Ionic dyes, sometimes called semi-permanent dyes, do not damage hair, but can cause skin coloration during hair dyeing. In addition, ionic dyes may flow down from the hair after 4 to 10 shampoo operations. Temporary dyes do not damage the hair and can wash off the skin coloring, but only one shampoo operation is possible. May flow out of the hair.
特許文献1~3には鉄塩を利用した金属染毛剤が記載されているが、皮膚着色については記載がない。特許文献4においては、毛髪の損傷を防止して施術後の毛髪に優れた指どおり性と、艶を付与することを目的とするものであり、染毛剤としては酸化染毛剤に限定されている。また、特許文献5はステインリムーバー配合用組成物に関するものであり、染毛剤に関するものではない。即ち、特許文献5の組成物は、皮膚に着色した酸化染料又はイオン染料を除去するためのものであり、染毛剤の皮膚着色を予防するものではない。染毛剤においては、染毛性を高めようとすると皮膚着色が起りやすくなり、皮膚着色を抑えようとすると染毛性が低くなってしまうという問題がある。本発明は、染毛性が良くかつ皮膚着色の少ない染毛剤及び染毛方法を提供することを解決すべき課題とした。
Patent Documents 1 to 3 describe metal hair dyes using iron salts, but do not describe skin coloring. In patent document 4, it aims at preventing the damage of hair and giving the excellent fingering property and gloss to the hair after treatment, and it is limited to an oxidation hair dye as a hair dye. ing. Patent Document 5 relates to a composition for compounding a stain remover, not a hair dye. That is, the composition of patent document 5 is for removing the oxidation dye or ionic dye colored on the skin, and does not prevent skin coloring of the hair dye. In hair dyes, there is a problem that skin coloring tends to occur when trying to improve hair coloring, and hair coloring becomes low when trying to suppress skin coloring. This invention made it the subject which should be solved to provide the hair dye and hair dyeing method with favorable hair dyeing property and little skin coloring.
本発明者らは上記課題を解決するために鋭意検討した結果、鉄と反応して発色する物質含む第1剤、及び鉄塩を含む第2剤を含む染毛剤において、第1剤の全質量に対して0.1質量%~12質量%の親水性基を有するメチルグルコシドを第1剤に配合することによって、上記課題を解決できることを見出し、本発明を完成するに至った。
As a result of intensive studies to solve the above problems, the present inventors have found that the first agent containing a substance that develops color by reacting with iron and the hair dye containing the second agent containing an iron salt, all of the first agent. It has been found that the above-mentioned problems can be solved by blending methyl glucoside having a hydrophilic group of 0.1% by mass to 12% by mass with respect to the mass into the first agent, and the present invention has been completed.
即ち、本発明によれば、以下の発明が提供される。
(1)鉄と反応して発色する物質、及び第1剤の全質量に対して0.1質量%~12質量%の下記式1で示される化合物を含む第1剤;並びに
鉄塩を含む第2剤;
を含む染毛剤。
式中、X1~X4はそれぞれ独立に単結合又は親水性基を示し、但し、X1~X4のうち少なくとも1以上は親水性基を示す。
(2)親水性基が、ポリオキシアルキレン基である、(1)に記載の染毛剤。
(3)式1で示される化合物が、下記式1Aで示される化合物である、(1)又は(2)に記載の染毛剤。
式中、Aはそれぞれ独立に、エチレン基又はプロピレン基を示す。a、b、c及びdはそれぞれ独立に0以上の整数を示し、但し、a、b、c及びdの合計は5~30の整数である。
(4)式1で示される化合物が、ポリオキシエチレンの付加モル数が10~20であるポリオキシエチレンメチルグルコシド、あるいはポリオキシプロピレンの付加モル数が10~20であるポリオキシプロピレンメチルグルコシドである、(1)から(3)の何れかに記載の染毛剤。
(5)上記の鉄と反応して発色する物質が、タンニン酸、サリチル酸及びサリチル酸誘導体、ピロガロール、没食子酸およびその誘導体、五倍子、ログウッド、ヘマテイン、カテコール、フタル酸、オイゲノール、イソオイゲノール、ニコチン酸アミド、デヒドロ酢酸、ピリドキシン、エラグ酸、コウジ酸、マルトール、フェルラ酸、ヒノキチオール、ウコンエキス、クルクミン、オウゴンエキス、タマネギエキス、クエルセチン、ルチン、ヘスペレチン、ヘスペリジン、生コーヒー豆抽出物、カフェー酸、クロロゲン酸、チャエキス、カテキン、エピカテキン、シコンエキス、シソエキス、シソニン、ブドウ葉エキス、ブトウエキス、エノシアニン、ラッカイン酸、ラック、コチニール、カルミン酸、エルダーベリー、アカキャベツ、ムラサキイモ、タマリンド、コウリャン、アピゲニニジン、及びルテオリニジンからなる群から選択される少なくとも1種以上である、(1)から(4)の何れかに記載の染毛剤。
(6)上記の鉄と反応して発色する物質が、タンニン酸と、サリチル酸又はサリチル酸誘導体との組み合わせ、又はピロガロールと、没食子酸又はその誘導体との組み合わせである、(1)から(5)の何れかに記載の染毛剤。
(7) 上記第1剤が、2-ヒドロキシベンゾフェノン骨格を有する紫外線吸収剤を更に含む、(1)から(6)の何れかに記載の染毛剤。
(8) 上記第1剤が、第1剤の全質量に対して0.5質量%~10質量%のアンモニウム塩を更に含む、(1)から(7)の何れかに記載の染毛剤。
(9) 上記第1剤が、第1剤の全質量に対して1質量%~12質量%のベンジルアルコールを更に含む、(1)から(8)の何れかに記載の染毛剤。
(10) 上記第1剤が、酸化防止剤を更に含む、(1)から(9)の何れかに記載の染毛剤。
(11)上記第1剤が、鉄と反応して発色する物質として、タンニン酸と、サリチル酸又はサリチル酸誘導体との組み合わせ、又はピロガロールと、没食子酸又はその誘導体との組み合わせを含み、式1で示される化合物として、ポリオキシエチレンの付加モル数が10又は20であるポリオキシエチレンメチルグルコシド、あるいはポリオキシプロピレンの付加モル数が10又は20であるポリオキシプロピレンメチルグルコシドを含み、2-ヒドロキシベンゾフェノン骨格を有する紫外線吸収剤としてオキシベンゼン-4、オキシベンゼン-3又はオキシベンゼン-1を含み、第1剤の全質量に対して0.5質量%~10質量%の炭酸水素アンモニウムを更に含み、第1剤の全質量に対して1質量%~12質量%のベンジルアルコールを更に含み、酸化防止剤として亜硫酸ナトリウムを更に含む、(1)から(10)の何れかに記載の染毛剤。
(12)上記鉄塩が、硫酸第一鉄、塩化第一鉄、酢酸第一鉄、硫酸第二鉄、塩酸第二鉄及び酢酸第二鉄からなる群より選ばれる少なくとも1種である、(1)から(11)の何れかに記載の染毛剤。
(13) (1)から(12)の何れかに記載の染毛剤を毛髪に付与することを含む毛髪の染毛方法。 That is, according to the present invention, the following inventions are provided.
(1) a substance that develops color by reacting with iron, and a first agent containing 0.1% by mass to 12% by mass of a compound represented by the following formula 1 with respect to the total mass of the first agent; and an iron salt Second agent;
Hair dye containing.
In the formula, X 1 to X 4 each independently represent a single bond or a hydrophilic group, provided that at least one of X 1 to X 4 represents a hydrophilic group.
(2) The hair dye according to (1), wherein the hydrophilic group is a polyoxyalkylene group.
(3) The hair dye according to (1) or (2), wherein the compound represented by the formula 1 is a compound represented by the following formula 1A.
In the formula, each A independently represents an ethylene group or a propylene group. a, b, c and d each independently represent an integer of 0 or more, provided that the sum of a, b, c and d is an integer of 5 to 30.
(4) The compound represented by Formula 1 is polyoxyethylene methyl glucoside having an addition mole number of polyoxyethylene of 10 to 20, or polyoxypropylene methyl glucoside having an addition mole number of polyoxypropylene of 10 to 20. The hair dye according to any one of (1) to (3).
(5) Substances that react with iron and develop color are tannic acid, salicylic acid and salicylic acid derivatives, pyrogallol, gallic acid and its derivatives, pentaploid, logwood, hematein, catechol, phthalic acid, eugenol, isoeugenol, nicotinic acid Amide, dehydroacetic acid, pyridoxine, ellagic acid, kojic acid, maltol, ferulic acid, hinokitiol, turmeric extract, curcumin, ougon extract, onion extract, quercetin, rutin, hesperetin, hesperidin, fresh coffee bean extract, caffeic acid, chlorogenic acid , Tea extract, catechin, epicatechin, shikon extract, shiso extract, shisonin, grape leaf extract, butto extract, enocyanin, lacainate, lac, cochineal, carminic acid, elderberry, red cabbage, mura Kiimo, tamarind, sorghum, Apigeninijin, and at least one member selected from the group consisting of Ruteorinijin, hair dye according to any one of (4) (1).
(6) The substance that develops color by reacting with iron is a combination of tannic acid and salicylic acid or a salicylic acid derivative, or a combination of pyrogallol and gallic acid or a derivative thereof. The hair dye according to any one of the above.
(7) The hair dye according to any one of (1) to (6), wherein the first agent further contains an ultraviolet absorber having a 2-hydroxybenzophenone skeleton.
(8) The hair dye according to any one of (1) to (7), wherein the first agent further contains 0.5% by mass to 10% by mass of an ammonium salt based on the total mass of the first agent. .
(9) The hair dye according to any one of (1) to (8), wherein the first agent further contains 1% by mass to 12% by mass of benzyl alcohol with respect to the total mass of the first agent.
(10) The hair dye according to any one of (1) to (9), wherein the first agent further contains an antioxidant.
(11) The first agent includes a combination of tannic acid and salicylic acid or a salicylic acid derivative, or a combination of pyrogallol and gallic acid or a derivative thereof as a substance that develops color by reacting with iron, and is represented by Formula 1. And a polyhydroxyethylene methyl glucoside having an addition mole number of polyoxyethylene of 10 or 20, or a polyoxypropylene methyl glucoside having an addition mole number of polyoxypropylene of 10 or 20, and a 2-hydroxybenzophenone skeleton Oxybenzene-4, oxybenzene-3 or oxybenzene-1 as an ultraviolet absorber having the following content: 0.5 wt% to 10 wt% ammonium hydrogen carbonate based on the total weight of the first agent, 1% by mass to 12% by mass of benzyl alcohol based on the total mass of one agent To include further includes sodium sulfite as an antioxidant, hair dye according to any one of (1) to (10).
(12) The iron salt is at least one selected from the group consisting of ferrous sulfate, ferrous chloride, ferrous acetate, ferric sulfate, ferric hydrochloride and ferric acetate. The hair dye according to any one of 1) to 11).
(13) A hair dyeing method comprising applying the hair dye according to any one of (1) to (12) to hair.
(1)鉄と反応して発色する物質、及び第1剤の全質量に対して0.1質量%~12質量%の下記式1で示される化合物を含む第1剤;並びに
鉄塩を含む第2剤;
を含む染毛剤。
(2)親水性基が、ポリオキシアルキレン基である、(1)に記載の染毛剤。
(3)式1で示される化合物が、下記式1Aで示される化合物である、(1)又は(2)に記載の染毛剤。
(4)式1で示される化合物が、ポリオキシエチレンの付加モル数が10~20であるポリオキシエチレンメチルグルコシド、あるいはポリオキシプロピレンの付加モル数が10~20であるポリオキシプロピレンメチルグルコシドである、(1)から(3)の何れかに記載の染毛剤。
(5)上記の鉄と反応して発色する物質が、タンニン酸、サリチル酸及びサリチル酸誘導体、ピロガロール、没食子酸およびその誘導体、五倍子、ログウッド、ヘマテイン、カテコール、フタル酸、オイゲノール、イソオイゲノール、ニコチン酸アミド、デヒドロ酢酸、ピリドキシン、エラグ酸、コウジ酸、マルトール、フェルラ酸、ヒノキチオール、ウコンエキス、クルクミン、オウゴンエキス、タマネギエキス、クエルセチン、ルチン、ヘスペレチン、ヘスペリジン、生コーヒー豆抽出物、カフェー酸、クロロゲン酸、チャエキス、カテキン、エピカテキン、シコンエキス、シソエキス、シソニン、ブドウ葉エキス、ブトウエキス、エノシアニン、ラッカイン酸、ラック、コチニール、カルミン酸、エルダーベリー、アカキャベツ、ムラサキイモ、タマリンド、コウリャン、アピゲニニジン、及びルテオリニジンからなる群から選択される少なくとも1種以上である、(1)から(4)の何れかに記載の染毛剤。
(6)上記の鉄と反応して発色する物質が、タンニン酸と、サリチル酸又はサリチル酸誘導体との組み合わせ、又はピロガロールと、没食子酸又はその誘導体との組み合わせである、(1)から(5)の何れかに記載の染毛剤。
(7) 上記第1剤が、2-ヒドロキシベンゾフェノン骨格を有する紫外線吸収剤を更に含む、(1)から(6)の何れかに記載の染毛剤。
(8) 上記第1剤が、第1剤の全質量に対して0.5質量%~10質量%のアンモニウム塩を更に含む、(1)から(7)の何れかに記載の染毛剤。
(9) 上記第1剤が、第1剤の全質量に対して1質量%~12質量%のベンジルアルコールを更に含む、(1)から(8)の何れかに記載の染毛剤。
(10) 上記第1剤が、酸化防止剤を更に含む、(1)から(9)の何れかに記載の染毛剤。
(11)上記第1剤が、鉄と反応して発色する物質として、タンニン酸と、サリチル酸又はサリチル酸誘導体との組み合わせ、又はピロガロールと、没食子酸又はその誘導体との組み合わせを含み、式1で示される化合物として、ポリオキシエチレンの付加モル数が10又は20であるポリオキシエチレンメチルグルコシド、あるいはポリオキシプロピレンの付加モル数が10又は20であるポリオキシプロピレンメチルグルコシドを含み、2-ヒドロキシベンゾフェノン骨格を有する紫外線吸収剤としてオキシベンゼン-4、オキシベンゼン-3又はオキシベンゼン-1を含み、第1剤の全質量に対して0.5質量%~10質量%の炭酸水素アンモニウムを更に含み、第1剤の全質量に対して1質量%~12質量%のベンジルアルコールを更に含み、酸化防止剤として亜硫酸ナトリウムを更に含む、(1)から(10)の何れかに記載の染毛剤。
(12)上記鉄塩が、硫酸第一鉄、塩化第一鉄、酢酸第一鉄、硫酸第二鉄、塩酸第二鉄及び酢酸第二鉄からなる群より選ばれる少なくとも1種である、(1)から(11)の何れかに記載の染毛剤。
(13) (1)から(12)の何れかに記載の染毛剤を毛髪に付与することを含む毛髪の染毛方法。 That is, according to the present invention, the following inventions are provided.
(1) a substance that develops color by reacting with iron, and a first agent containing 0.1% by mass to 12% by mass of a compound represented by the following formula 1 with respect to the total mass of the first agent; and an iron salt Second agent;
Hair dye containing.
(2) The hair dye according to (1), wherein the hydrophilic group is a polyoxyalkylene group.
(3) The hair dye according to (1) or (2), wherein the compound represented by the formula 1 is a compound represented by the following formula 1A.
(4) The compound represented by Formula 1 is polyoxyethylene methyl glucoside having an addition mole number of polyoxyethylene of 10 to 20, or polyoxypropylene methyl glucoside having an addition mole number of polyoxypropylene of 10 to 20. The hair dye according to any one of (1) to (3).
(5) Substances that react with iron and develop color are tannic acid, salicylic acid and salicylic acid derivatives, pyrogallol, gallic acid and its derivatives, pentaploid, logwood, hematein, catechol, phthalic acid, eugenol, isoeugenol, nicotinic acid Amide, dehydroacetic acid, pyridoxine, ellagic acid, kojic acid, maltol, ferulic acid, hinokitiol, turmeric extract, curcumin, ougon extract, onion extract, quercetin, rutin, hesperetin, hesperidin, fresh coffee bean extract, caffeic acid, chlorogenic acid , Tea extract, catechin, epicatechin, shikon extract, shiso extract, shisonin, grape leaf extract, butto extract, enocyanin, lacainate, lac, cochineal, carminic acid, elderberry, red cabbage, mura Kiimo, tamarind, sorghum, Apigeninijin, and at least one member selected from the group consisting of Ruteorinijin, hair dye according to any one of (4) (1).
(6) The substance that develops color by reacting with iron is a combination of tannic acid and salicylic acid or a salicylic acid derivative, or a combination of pyrogallol and gallic acid or a derivative thereof. The hair dye according to any one of the above.
(7) The hair dye according to any one of (1) to (6), wherein the first agent further contains an ultraviolet absorber having a 2-hydroxybenzophenone skeleton.
(8) The hair dye according to any one of (1) to (7), wherein the first agent further contains 0.5% by mass to 10% by mass of an ammonium salt based on the total mass of the first agent. .
(9) The hair dye according to any one of (1) to (8), wherein the first agent further contains 1% by mass to 12% by mass of benzyl alcohol with respect to the total mass of the first agent.
(10) The hair dye according to any one of (1) to (9), wherein the first agent further contains an antioxidant.
(11) The first agent includes a combination of tannic acid and salicylic acid or a salicylic acid derivative, or a combination of pyrogallol and gallic acid or a derivative thereof as a substance that develops color by reacting with iron, and is represented by Formula 1. And a polyhydroxyethylene methyl glucoside having an addition mole number of polyoxyethylene of 10 or 20, or a polyoxypropylene methyl glucoside having an addition mole number of polyoxypropylene of 10 or 20, and a 2-hydroxybenzophenone skeleton Oxybenzene-4, oxybenzene-3 or oxybenzene-1 as an ultraviolet absorber having the following content: 0.5 wt% to 10 wt% ammonium hydrogen carbonate based on the total weight of the first agent, 1% by mass to 12% by mass of benzyl alcohol based on the total mass of one agent To include further includes sodium sulfite as an antioxidant, hair dye according to any one of (1) to (10).
(12) The iron salt is at least one selected from the group consisting of ferrous sulfate, ferrous chloride, ferrous acetate, ferric sulfate, ferric hydrochloride and ferric acetate. The hair dye according to any one of 1) to 11).
(13) A hair dyeing method comprising applying the hair dye according to any one of (1) to (12) to hair.
本発明の染毛剤及び染毛方法によれば、良好な染毛性を維持したまま、皮膚着色を低減することができる。
According to the hair dye and hair dyeing method of the present invention, skin coloring can be reduced while maintaining good hair dyeing properties.
以下、本発明の実施の形態について詳細に説明する。本明細書において「~」を用いて示された数値範囲は、「~」の前後に記載される数値をそれぞれ最小値及び最大値として含む範囲を示す。
Hereinafter, embodiments of the present invention will be described in detail. In the present specification, a numerical range indicated by using “to” indicates a range including the numerical values described before and after “to” as the minimum value and the maximum value, respectively.
[染毛剤]
本発明の染毛剤は、鉄と反応して発色する物質、及び第1剤の全質量に対して0.1質量%~12質量%の式1で示される化合物を含む第1剤;並びに鉄塩を含む第2剤を組み合わせて含む2剤式の染毛剤である。本発明においては、第1剤に、式1で示される化合物を添加することによって、良好な染毛性と皮膚着色の抑制とを同時に達成することが可能になった。 [Hair dye]
The hair dye of the present invention comprises a substance that develops color by reacting with iron, and a first agent comprising 0.1% by mass to 12% by mass of the compound represented by formula 1 with respect to the total mass of the first agent; It is a two-component hair dye containing a combination of a second agent containing an iron salt. In the present invention, by adding the compound represented by Formula 1 to the first agent, it has become possible to simultaneously achieve good hair dyeing properties and suppression of skin coloring.
本発明の染毛剤は、鉄と反応して発色する物質、及び第1剤の全質量に対して0.1質量%~12質量%の式1で示される化合物を含む第1剤;並びに鉄塩を含む第2剤を組み合わせて含む2剤式の染毛剤である。本発明においては、第1剤に、式1で示される化合物を添加することによって、良好な染毛性と皮膚着色の抑制とを同時に達成することが可能になった。 [Hair dye]
The hair dye of the present invention comprises a substance that develops color by reacting with iron, and a first agent comprising 0.1% by mass to 12% by mass of the compound represented by formula 1 with respect to the total mass of the first agent; It is a two-component hair dye containing a combination of a second agent containing an iron salt. In the present invention, by adding the compound represented by Formula 1 to the first agent, it has become possible to simultaneously achieve good hair dyeing properties and suppression of skin coloring.
<第1剤>
第1剤は、第1剤の全質量に対して0.1質量%~12質量%の下記式1で示される化合物を含む。
式中、X1~X4はそれぞれ独立に単結合又は親水性基を示し、但し、X1~X4のうち少なくとも1以上は親水性基を示す。
<First Agent>
The first agent contains 0.1% by mass to 12% by mass of the compound represented by the following formula 1 with respect to the total mass of the first agent.
In the formula, X 1 to X 4 each independently represent a single bond or a hydrophilic group, provided that at least one of X 1 to X 4 represents a hydrophilic group.
第1剤は、第1剤の全質量に対して0.1質量%~12質量%の下記式1で示される化合物を含む。
The first agent contains 0.1% by mass to 12% by mass of the compound represented by the following formula 1 with respect to the total mass of the first agent.
X1~X4が示す親水性基は、2価の親水性基であり、その種類は特に限定されないが、ノニオン性親水性基が好ましい。ノニオン性親水性基としては、ポリオキシアルキレン基などが挙げられる。上記アルキレン中の炭素原子数は特に限定されないが、好ましくは1~5であり、より好ましくは2~4であり、特に好ましくは2又は3である。ポリオキシアルキレン基としては、例えば、ポリオキシエチレン基、ポリオキシプロピレレ基、ポリオキシエチレン-ポリオキシプロピレン基、ポリオキシエチレン-ポリオキシプロピレン-オキシブチレン基などが挙げられる。上記の中でも、良好な染毛性と皮膚着色の抑制の観点から、ポリオキシエチレン基が好ましい。
The hydrophilic group represented by X 1 to X 4 is a divalent hydrophilic group, and the type thereof is not particularly limited, but a nonionic hydrophilic group is preferable. Examples of the nonionic hydrophilic group include a polyoxyalkylene group. The number of carbon atoms in the above alkylene is not particularly limited, but is preferably 1 to 5, more preferably 2 to 4, and particularly preferably 2 or 3. Examples of the polyoxyalkylene group include a polyoxyethylene group, a polyoxypropylene group, a polyoxyethylene-polyoxypropylene group, a polyoxyethylene-polyoxypropylene-oxybutylene group, and the like. Among these, a polyoxyethylene group is preferable from the viewpoint of good hair dyeability and suppression of skin coloring.
式1で示される化合物としては、好ましくは下記式1Aで示される化合物である。
式中、Aはそれぞれ独立に、エチレン基又はプロピレン基を示す。a、b、c及びdはそれぞれ独立に0以上の整数を示す。但し、ポリオキシアルキレンの付加モル数(a+b+c+dの合計)は5~30の整数であり、5~25の整数が好ましく、10~20の整数がより好ましい。
The compound represented by the formula 1 is preferably a compound represented by the following formula 1A.
In the formula, each A independently represents an ethylene group or a propylene group. a, b, c and d each independently represent an integer of 0 or more. However, the added mole number of polyoxyalkylene (total of a + b + c + d) is an integer of 5 to 30, preferably an integer of 5 to 25, and more preferably an integer of 10 to 20.
式1で示される化合物の特に好ましい例としては、ポリオキシエチレンの付加モル数が10~20(例えば、10又は20)であるポリオキシエチレンメチルグルコシド、あるいはポリオキシプロピレンの付加モル数が10~20(例えば、10又は20)であるポリオキシプロピレンメチルグルコシドである。
Particularly preferred examples of the compound represented by Formula 1 include polyoxyethylene methylglucoside having a polyoxyethylene addition mole number of 10 to 20 (for example, 10 or 20), or polyoxypropylene addition mole number of 10 to Polyoxypropylene methyl glucoside that is 20 (eg 10 or 20).
式1で示される化合物としては、例えば、以下の日油株式会社製市販品を使用することができる。
マクビオブライド(登録商標)MG-10E:
ポリオキシエチレンの付加モル数が10であるポリオキシエチレンメチルグルコシド
マクビオブライド(登録商標)MG-20E:
ポリオキシエチレンの付加モル数が10であるポリオキシエチレンメチルグルコシド
マクビオブライド(登録商標)MG-10P:
ポリオキシプロピレンの付加モル数が10であるポリオキシプロピレンメチルグルコシド
マクビオブライド(登録商標)MG-20P:
ポリオキシプロピレンの付加モル数が20であるポリオキシプロピレンメチルグルコシド As the compound represented by Formula 1, for example, the following commercial products manufactured by NOF Corporation can be used.
Macbiobride® MG-10E:
Polyoxyethylene methyl glucoside macbiobroide (registered trademark) MG-20E having an addition mole number of polyoxyethylene of 10:
Polyoxyethylene methyl glucoside macbiobroide (registered trademark) MG-10P having a polyoxyethylene addition mole number of 10:
Polyoxypropylene methylglucoside macbiobroide (registered trademark) MG-20P in which the number of moles of polyoxypropylene added is 10:
Polyoxypropylene methylglucoside having an addition mole number of polyoxypropylene of 20.
マクビオブライド(登録商標)MG-10E:
ポリオキシエチレンの付加モル数が10であるポリオキシエチレンメチルグルコシド
マクビオブライド(登録商標)MG-20E:
ポリオキシエチレンの付加モル数が10であるポリオキシエチレンメチルグルコシド
マクビオブライド(登録商標)MG-10P:
ポリオキシプロピレンの付加モル数が10であるポリオキシプロピレンメチルグルコシド
マクビオブライド(登録商標)MG-20P:
ポリオキシプロピレンの付加モル数が20であるポリオキシプロピレンメチルグルコシド As the compound represented by Formula 1, for example, the following commercial products manufactured by NOF Corporation can be used.
Macbiobride® MG-10E:
Polyoxyethylene methyl glucoside macbiobroide (registered trademark) MG-20E having an addition mole number of polyoxyethylene of 10:
Polyoxyethylene methyl glucoside macbiobroide (registered trademark) MG-10P having a polyoxyethylene addition mole number of 10:
Polyoxypropylene methylglucoside macbiobroide (registered trademark) MG-20P in which the number of moles of polyoxypropylene added is 10:
Polyoxypropylene methylglucoside having an addition mole number of polyoxypropylene of 20.
ウィルブライト(登録商標)MG-2070:
AOはエチレンオキシドとプロピレンオキシドのランダム共重合体を示し、BOはブチレンオキシドを示す。
Wilbright (R) MG-2070:
AO represents a random copolymer of ethylene oxide and propylene oxide, and BO represents butylene oxide.
式1で示される化合物は1種類の化合物を使用してもよいし、2種類以上の化合物を併用してもよい。
式1で示される化合物の含有量は、第1剤の全質量に対して0.1質量%~12質量%であり、0.2質量%~10質量%であることが好ましく0.5質量%~5質量%であることがより好ましく、2質量%~3質量%であることが最も好ましい。2種類以上の式1で示される化合物を併用する場合には、合計の含有量が上記範囲になることが好ましい。式1で示される化合物の含有量を上記範囲とすることによって、良好な染毛性と皮膚着色の抑制を同時に達成することが可能になり、さらに染毛剤の高い保存安定性を達成することができる。 As the compound represented by Formula 1, one type of compound may be used, or two or more types of compounds may be used in combination.
The content of the compound represented by Formula 1 is 0.1% by mass to 12% by mass with respect to the total mass of the first agent, and preferably 0.2% by mass to 10% by mass. % To 5% by mass is more preferable, and 2% to 3% by mass is most preferable. When two or more compounds represented by Formula 1 are used in combination, the total content is preferably within the above range. By setting the content of the compound represented by Formula 1 within the above range, it becomes possible to achieve good hair dyeing properties and suppression of skin coloring at the same time, and further achieve high storage stability of the hair dye. Can do.
式1で示される化合物の含有量は、第1剤の全質量に対して0.1質量%~12質量%であり、0.2質量%~10質量%であることが好ましく0.5質量%~5質量%であることがより好ましく、2質量%~3質量%であることが最も好ましい。2種類以上の式1で示される化合物を併用する場合には、合計の含有量が上記範囲になることが好ましい。式1で示される化合物の含有量を上記範囲とすることによって、良好な染毛性と皮膚着色の抑制を同時に達成することが可能になり、さらに染毛剤の高い保存安定性を達成することができる。 As the compound represented by Formula 1, one type of compound may be used, or two or more types of compounds may be used in combination.
The content of the compound represented by Formula 1 is 0.1% by mass to 12% by mass with respect to the total mass of the first agent, and preferably 0.2% by mass to 10% by mass. % To 5% by mass is more preferable, and 2% to 3% by mass is most preferable. When two or more compounds represented by Formula 1 are used in combination, the total content is preferably within the above range. By setting the content of the compound represented by Formula 1 within the above range, it becomes possible to achieve good hair dyeing properties and suppression of skin coloring at the same time, and further achieve high storage stability of the hair dye. Can do.
本発明で用いる鉄と反応して発色する物質としては、鉄と反応して発色する有機化合物又は植物抽出物を使用することができる。鉄と反応して発色する物質の具体例としては、タンニン酸、サリチル酸及びサリチル酸誘導体、ピロガロール、没食子酸およびその誘導体、五倍子、ログウッド、ヘマテイン、カテコール、フタル酸、オイゲノール、イソオイゲノール、ニコチン酸アミド、デヒドロ酢酸、ピリドキシン、エラグ酸、コウジ酸、マルトール、フェルラ酸、ヒノキチオール、ウコンエキス、クルクミン、オウゴンエキス、タマネギエキス、クエルセチン、ルチン、ヘスペレチン、ヘスペリジン、生コーヒー豆抽出物、カフェー酸、クロロゲン酸、チャエキス、カテキン、エピカテキン、シコンエキス、シソエキス、シソニン、ブドウ葉エキス、ブトウエキス、エノシアニン、ラッカイン酸、ラック、コチニール、カルミン酸、エルダーベリー、アカキャベツ、ムラサキイモ、タマリンド、コウリャン、アピゲニニジン、及びルテオリニジンから選択される少なくとも1種以上を挙げることができるが、これらに限定されるものではない。上記の中でもより好ましくは、タンニン酸、サリチル酸およびその誘導体、ピロガロール、並びに没食子酸およびその誘導体から選択される1種以上である。鉄と反応して発色する物質としては、タンニン酸と、サリチル酸又はサリチル酸誘導体との組み合わせ、又はピロガロールと、没食子酸又はその誘導体との組み合わせが特に好ましい。
As the substance that develops color by reacting with iron used in the present invention, an organic compound or plant extract that develops color by reacting with iron can be used. Specific examples of substances that develop color by reacting with iron include tannic acid, salicylic acid and salicylic acid derivatives, pyrogallol, gallic acid and its derivatives, pentaploid, logwood, hematein, catechol, phthalic acid, eugenol, isoeugenol, nicotinamide , Dehydroacetic acid, pyridoxine, ellagic acid, kojic acid, maltol, ferulic acid, hinokitiol, turmeric extract, curcumin, ougon extract, onion extract, quercetin, rutin, hesperetin, hesperidin, raw coffee bean extract, caffeic acid, chlorogenic acid, Cha extract, catechin, epicatechin, shikon extract, perilla extract, shisonin, grape leaf extract, butter extract, enocyanin, lacainate, lac, cochineal, carminic acid, elderberry, red cabbage, mu Sakiimo, tamarind, sorghum, Apigeninijin, and can include at least one or more selected from Ruteorinijin, but is not limited thereto. Among these, more preferable is at least one selected from tannic acid, salicylic acid and derivatives thereof, pyrogallol, and gallic acid and derivatives thereof. The substance that develops color by reacting with iron is particularly preferably a combination of tannic acid and salicylic acid or a salicylic acid derivative, or a combination of pyrogallol and gallic acid or a derivative thereof.
没食子酸の誘導体としては、例えば、没食子酸のアルキルエステルが挙げられ、没食子酸のアルキルエステルとしては、例えば、炭素数1~10、好ましくは2~5の直鎖状又は分岐状のアルキルエステルが挙げられる。例えば、没食子酸エチル、没食子酸プロピル、没食子酸イソアミルなどが含まれる。没食子酸又はその誘導体は、公知の方法により化学合成したものでもよく、植物から単離したものでもよい。植物から単離したものに更に化学合成を加えたものでもよい。また、植物から得られる没食子酸又はその誘導体を含有するエキスをそのまま用いてもよい。例えば、マメ科植物タラ由来の没食子酸やウルシ科ヌルデに発生する五倍子由来の没食子酸又はそれらを含有するエキスなどを用いることができる。またそれらの没食子酸を化学的にエステル化して得られた誘導体を用いることもできる。サリチル酸の誘導体としては、サリチル酸のエステルや塩が含まれる。サリチル酸の塩としては、サリチル酸のアルカリ金属塩が挙げられる。具体的にはサリチル酸ナトリウムが挙げられる。またサリチル酸のエステルとしては、サリチル酸メチル、サリチル酸エチルなどが挙げられる。
Examples of derivatives of gallic acid include alkyl esters of gallic acid, and examples of alkyl esters of gallic acid include linear or branched alkyl esters having 1 to 10 carbon atoms, preferably 2 to 5 carbon atoms. Can be mentioned. For example, ethyl gallate, propyl gallate, isoamyl gallate and the like are included. Gallic acid or a derivative thereof may be chemically synthesized by a known method or may be isolated from a plant. What further added chemical synthesis to what was isolated from the plant may be used. Moreover, you may use the extract containing the gallic acid obtained from a plant, or its derivative (s) as it is. For example, gallic acid derived from leguminous plant cod, gallic acid derived from pentaploid which occurs in urchinaceae, or extracts containing them can be used. In addition, derivatives obtained by chemically esterifying those gallic acids can also be used. Salicylic acid derivatives include salicylic acid esters and salts. Examples of the salicylic acid salt include alkali metal salts of salicylic acid. Specific examples include sodium salicylate. Examples of the salicylic acid ester include methyl salicylate and ethyl salicylate.
鉄と反応して発色する物質は1種類の化合物を使用してもよいし、2種類以上の化合物を併用してもよい。
鉄と反応して発色する物質の含有量は、第1剤の全質量に対して0.5質量%~10質量%であることが好ましく、0.5質量%~6質量%であることがより好ましい。鉄と反応して発色する物質を2種類以上使用する場合には、合計の含有量が上記範囲になることが好ましい。鉄と反応して発色する物質の含有量を上記範囲とすることによって、良好な染毛性を達成することが可能になる。 As the substance that reacts with iron and develops color, one kind of compound may be used, or two or more kinds of compounds may be used in combination.
The content of the substance that develops color by reacting with iron is preferably 0.5% by mass to 10% by mass, and preferably 0.5% by mass to 6% by mass with respect to the total mass of the first agent. More preferred. When two or more kinds of substances that react with iron and develop color are used, the total content is preferably within the above range. By setting the content of the substance that develops color by reacting with iron within the above range, it is possible to achieve good hair dyeing properties.
鉄と反応して発色する物質の含有量は、第1剤の全質量に対して0.5質量%~10質量%であることが好ましく、0.5質量%~6質量%であることがより好ましい。鉄と反応して発色する物質を2種類以上使用する場合には、合計の含有量が上記範囲になることが好ましい。鉄と反応して発色する物質の含有量を上記範囲とすることによって、良好な染毛性を達成することが可能になる。 As the substance that reacts with iron and develops color, one kind of compound may be used, or two or more kinds of compounds may be used in combination.
The content of the substance that develops color by reacting with iron is preferably 0.5% by mass to 10% by mass, and preferably 0.5% by mass to 6% by mass with respect to the total mass of the first agent. More preferred. When two or more kinds of substances that react with iron and develop color are used, the total content is preferably within the above range. By setting the content of the substance that develops color by reacting with iron within the above range, it is possible to achieve good hair dyeing properties.
本発明において好ましくは、第1剤は、2-ヒドロキシベンゾフェノン骨格を有する紫外線吸収剤を更に含んでいてもよい。
2-ヒドロキシベンゾフェノン骨格を有する紫外線吸収剤としては、好ましくは、以下の一般式(2)で示される2-ヒドロキシベンゾフェノン骨格を有する化合物を使用することができる。 In the present invention, preferably, the first agent may further contain an ultraviolet absorber having a 2-hydroxybenzophenone skeleton.
As the ultraviolet absorber having a 2-hydroxybenzophenone skeleton, a compound having a 2-hydroxybenzophenone skeleton represented by the following general formula (2) can be preferably used.
2-ヒドロキシベンゾフェノン骨格を有する紫外線吸収剤としては、好ましくは、以下の一般式(2)で示される2-ヒドロキシベンゾフェノン骨格を有する化合物を使用することができる。 In the present invention, preferably, the first agent may further contain an ultraviolet absorber having a 2-hydroxybenzophenone skeleton.
As the ultraviolet absorber having a 2-hydroxybenzophenone skeleton, a compound having a 2-hydroxybenzophenone skeleton represented by the following general formula (2) can be preferably used.
2-ヒドロキシベンゾフェノン骨格を有する紫外線吸収剤の具体例としては、オキシベンゾン-1(2,4-ジヒドロキシベンゾフェノン)、オキシベンゾン-3(2-ヒドロキシ-4-メトキシベンフェノン)、オキシベンゾン-4(2-ヒドロキシ-4-メトキシベンゾフェノンスルホン酸)、オキシベンゾン-6(2,2’‐ジヒドロキシ‐4,4’‐ジメトキシベンゾフェノン)、テトラヒドロキシベンゾフェノン、オキシベンゾン-9(2,2’‐ジヒドロキシ‐4,4’‐ジメトキシベンゾフェノンジスルホン酸)、4-エトキシ-2-ヒドロキシベンフェノン、4-(2-エチルヘキシルオキシ)-2-ヒドロキシベンフェノン、5-アミノ-2-ヒドロキシベンゾフェノン、4-アミノ-2-ヒドロキシベンゾフェノン、4’-アミノ-2-ヒドロキシベンゾフェノン、2-ヒドロキシ-5-クロロベンゾフェノン、2-ヒドロキシ-3、5-ジクロロベンゾフェノン、3’,5-ジクロロ-2-ヒドロキシ-ベンゾフェノン、2-ヒドロキシ-4’-メチルベンゾフェノン、2-ヒドロキシ-4’-メトキシベンフェノン、2-ヒドロキシ-5-メチルベンフェノン、2-ヒドロキシ-4’-メチルベンフェノン、2-ヒドロキシ-3-tert-ブチルベンフェノンなどが挙げられるが、これらに限定されるものではない。上記の中でもより好ましくは、オキシベンゾン-1、オキシベンゾン-3、又はオキシベンゾン-4であり、特に好ましくはオキシベンゾン-4である。
Specific examples of the ultraviolet absorber having a 2-hydroxybenzophenone skeleton include oxybenzone-1 (2,4-dihydroxybenzophenone), oxybenzone-3 (2-hydroxy-4-methoxybenphenone), and oxybenzone-4 (2-hydroxybenzone-4). -4-methoxybenzophenonesulfonic acid), oxybenzone-6 (2,2'-dihydroxy-4,4'-dimethoxybenzophenone), tetrahydroxybenzophenone, oxybenzone-9 (2,2'-dihydroxy-4,4'-dimethoxy) Benzophenone disulfonic acid), 4-ethoxy-2-hydroxybenphenone, 4- (2-ethylhexyloxy) -2-hydroxybenphenone, 5-amino-2-hydroxybenzophenone, 4-amino-2-hydroxybenzophenone, '-Amino-2-hydroxybenzophenone, 2-hydroxy-5-chlorobenzophenone, 2-hydroxy-3, 5-dichlorobenzophenone, 3', 5-dichloro-2-hydroxy-benzophenone, 2-hydroxy-4'-methyl Examples include benzophenone, 2-hydroxy-4′-methoxybenphenone, 2-hydroxy-5-methylbenphenone, 2-hydroxy-4′-methylbenphenone, 2-hydroxy-3-tert-butylbenphenone, and the like. However, it is not limited to these. Among these, oxybenzone-1, oxybenzone-3, or oxybenzone-4 is more preferable, and oxybenzone-4 is particularly preferable.
2-ヒドロキシベンゾフェノン骨格を有する紫外線吸収剤としては、ClogPが1以上7以下である化合物を用いることが好ましい。ClogPが1以上7以下である化合物を用いることにより、特に良好な染色効果を達成することができる。その理由としては、ClogPが1以上7以下である化合物を用いることにより、本化合物も髪に浸透し、髪中で鉄キレートを形成し、染色に対して寄与するものと推定される。なお、logPは、疎水性を表すパラメーターで、水とオクタノールの分配係数を示す。近年の計算化学の発展により、コンピューター上において計算によりlogPの値を求めることができるようになり、その値のことをClopPと言う。
2-ヒドロキシベンゾフェノン骨格を有する紫外線吸収剤のうちの代表的な化合物の構造及びClogPを以下に記載する。 As the ultraviolet absorber having a 2-hydroxybenzophenone skeleton, a compound having a ClogP of 1 or more and 7 or less is preferably used. By using a compound having ClogP of 1 or more and 7 or less, a particularly good staining effect can be achieved. The reason for this is presumed that by using a compound having a ClogP of 1 or more and 7 or less, this compound also penetrates into the hair, forms an iron chelate in the hair, and contributes to dyeing. LogP is a parameter representing hydrophobicity and represents a partition coefficient between water and octanol. With the recent development of computational chemistry, the value of logP can be obtained by calculation on a computer, and this value is called ClopP.
The structure and ClogP of typical compounds among ultraviolet absorbers having a 2-hydroxybenzophenone skeleton are described below.
2-ヒドロキシベンゾフェノン骨格を有する紫外線吸収剤のうちの代表的な化合物の構造及びClogPを以下に記載する。 As the ultraviolet absorber having a 2-hydroxybenzophenone skeleton, a compound having a ClogP of 1 or more and 7 or less is preferably used. By using a compound having ClogP of 1 or more and 7 or less, a particularly good staining effect can be achieved. The reason for this is presumed that by using a compound having a ClogP of 1 or more and 7 or less, this compound also penetrates into the hair, forms an iron chelate in the hair, and contributes to dyeing. LogP is a parameter representing hydrophobicity and represents a partition coefficient between water and octanol. With the recent development of computational chemistry, the value of logP can be obtained by calculation on a computer, and this value is called ClopP.
The structure and ClogP of typical compounds among ultraviolet absorbers having a 2-hydroxybenzophenone skeleton are described below.
2-ヒドロキシベンゾフェノン骨格を有する紫外線吸収剤を使用する場合における使用量は特に限定されないが、第1剤の全質量に対して0.5質量%~10質量%であることが好ましく、1質量%~6質量%であることがより好ましい。2-ヒドロキシベンゾフェノン骨格を有する紫外線吸収剤を2種類以上使用する場合には、合計の含有量が上記範囲になることが好ましい。
The amount used in the case of using an ultraviolet absorber having a 2-hydroxybenzophenone skeleton is not particularly limited, but is preferably 0.5% by mass to 10% by mass with respect to the total mass of the first agent, and 1% by mass. More preferably, it is ˜6% by mass. When two or more kinds of ultraviolet absorbers having a 2-hydroxybenzophenone skeleton are used, the total content is preferably within the above range.
本発明において好ましくは、第1剤は、第1剤の全質量に対して0.5質量%~10質量%のアンモニウム塩を更に含んでいてもよい。
アンモニウム塩としては、具体的に炭酸水素アンモニウム、硫酸アンモニウム、酢酸アンモニウム、塩化アンモニウム、炭酸アンモニウム、硝酸アンモニウム、過塩素酸アンモニウム等が挙げられ、これらは1種単独で使用してもよく、2種以上を併用してもよい。特に好ましくは、炭酸水素アンモニウムを使用することができる。
アンモニウム塩を使用する場合、その含有量は特に限定されないが、0.5質量%~10質量%であることが好ましく、1質量%~5質量%であることがより好ましい。アンモニウム塩を2種類以上使用する場合には、合計の含有量が上記範囲になることが好ましい。 In the present invention, preferably, the first agent may further contain 0.5% by mass to 10% by mass of an ammonium salt based on the total mass of the first agent.
Specific examples of ammonium salts include ammonium bicarbonate, ammonium sulfate, ammonium acetate, ammonium chloride, ammonium carbonate, ammonium nitrate, ammonium perchlorate, and the like. These may be used alone or in combination of two or more. You may use together. Particularly preferably, ammonium hydrogen carbonate can be used.
When the ammonium salt is used, the content thereof is not particularly limited, but is preferably 0.5% by mass to 10% by mass, and more preferably 1% by mass to 5% by mass. When two or more kinds of ammonium salts are used, the total content is preferably within the above range.
アンモニウム塩としては、具体的に炭酸水素アンモニウム、硫酸アンモニウム、酢酸アンモニウム、塩化アンモニウム、炭酸アンモニウム、硝酸アンモニウム、過塩素酸アンモニウム等が挙げられ、これらは1種単独で使用してもよく、2種以上を併用してもよい。特に好ましくは、炭酸水素アンモニウムを使用することができる。
アンモニウム塩を使用する場合、その含有量は特に限定されないが、0.5質量%~10質量%であることが好ましく、1質量%~5質量%であることがより好ましい。アンモニウム塩を2種類以上使用する場合には、合計の含有量が上記範囲になることが好ましい。 In the present invention, preferably, the first agent may further contain 0.5% by mass to 10% by mass of an ammonium salt based on the total mass of the first agent.
Specific examples of ammonium salts include ammonium bicarbonate, ammonium sulfate, ammonium acetate, ammonium chloride, ammonium carbonate, ammonium nitrate, ammonium perchlorate, and the like. These may be used alone or in combination of two or more. You may use together. Particularly preferably, ammonium hydrogen carbonate can be used.
When the ammonium salt is used, the content thereof is not particularly limited, but is preferably 0.5% by mass to 10% by mass, and more preferably 1% by mass to 5% by mass. When two or more kinds of ammonium salts are used, the total content is preferably within the above range.
本発明において好ましくは、第1剤は、第1剤の全質量に対して1質量%~12質量%、より好ましくは1質量%~5質量%のベンジルアルコールを更に含んでいてもよい。ベンンジルアルコールを含むことで、キューティクルを膨潤させ、染毛性を向上させることができる。ベンジルアルコールは溶剤として使用することができる。
In the present invention, preferably, the first agent may further contain 1% by mass to 12% by mass, more preferably 1% by mass to 5% by mass, based on the total mass of the first agent. By containing benzil alcohol, it is possible to swell the cuticle and improve the hair dyeing property. Benzyl alcohol can be used as a solvent.
本発明において好ましくは、第1剤は、酸化防止剤を更に含んでいてもよい。
酸化防止剤としては、通常の染毛剤に使用できるものを用いることができ、亜硫酸塩、亜硫酸水素塩、チオ硫酸塩、アスコルビン酸類、チオグリコール酸類、システイン類、メルカプト化合物等が挙げられる。酸化防止剤として、具体的には、亜硫酸ナトリウム、L-アスコルビン酸及びその塩、チオグリコール酸及びその塩、L-システイン及びその塩、N-アセチル-L-システイン及びその塩が好ましいものとして挙げられる。中でも、亜硫酸ナトリウムは、染料前駆物質の安定化に寄与するだけでなく、染毛力をも向上させるため好ましい。酸化防止剤は、いずれかを1種単独で使用してもよく、2種以上を併用してもよい。 In the present invention, preferably, the first agent may further contain an antioxidant.
As antioxidant, what can be used for a normal hair dye can be used, and sulfite, bisulfite, thiosulfate, ascorbic acid, thioglycolic acid, cysteine, mercapto compound, etc. are mentioned. Specific examples of the antioxidant include sodium sulfite, L-ascorbic acid and its salt, thioglycolic acid and its salt, L-cysteine and its salt, and N-acetyl-L-cysteine and its salt. It is done. Among these, sodium sulfite is preferable because it not only contributes to the stabilization of the dye precursor, but also improves the hair dyeing power. Any one antioxidant may be used alone, or two or more antioxidants may be used in combination.
酸化防止剤としては、通常の染毛剤に使用できるものを用いることができ、亜硫酸塩、亜硫酸水素塩、チオ硫酸塩、アスコルビン酸類、チオグリコール酸類、システイン類、メルカプト化合物等が挙げられる。酸化防止剤として、具体的には、亜硫酸ナトリウム、L-アスコルビン酸及びその塩、チオグリコール酸及びその塩、L-システイン及びその塩、N-アセチル-L-システイン及びその塩が好ましいものとして挙げられる。中でも、亜硫酸ナトリウムは、染料前駆物質の安定化に寄与するだけでなく、染毛力をも向上させるため好ましい。酸化防止剤は、いずれかを1種単独で使用してもよく、2種以上を併用してもよい。 In the present invention, preferably, the first agent may further contain an antioxidant.
As antioxidant, what can be used for a normal hair dye can be used, and sulfite, bisulfite, thiosulfate, ascorbic acid, thioglycolic acid, cysteine, mercapto compound, etc. are mentioned. Specific examples of the antioxidant include sodium sulfite, L-ascorbic acid and its salt, thioglycolic acid and its salt, L-cysteine and its salt, and N-acetyl-L-cysteine and its salt. It is done. Among these, sodium sulfite is preferable because it not only contributes to the stabilization of the dye precursor, but also improves the hair dyeing power. Any one antioxidant may be used alone, or two or more antioxidants may be used in combination.
酸化防止剤を使用する場合、その含有量は特に限定されないが、第1剤の全質量に対して、0.5質量%~10質量%含有することが好ましく、1質量%~6質量%含有することがより好ましい。酸化防止剤を2種類以上使用する場合には、合計の含有量が上記範囲になることが好ましい。
When the antioxidant is used, its content is not particularly limited, but it is preferably 0.5% by mass to 10% by mass and preferably 1% by mass to 6% by mass with respect to the total mass of the first agent. More preferably. When using 2 or more types of antioxidant, it is preferable that total content becomes the said range.
本発明の染毛剤における第1剤の特に好ましい例としては、鉄と反応して発色する物質として、タンニン酸と、サリチル酸又はサリチル酸誘導体との組み合わせ、又はピロガロールと、没食子酸又はその誘導体との組み合わせを含み、式1で示される化合物として、ポリオキシエチレンの付加モル数が10又は20であるポリオキシエチレンメチルグルコシド、あるいはポリオキシプロピレンの付加モル数が10又は20であるポリオキシプロピレンメチルグルコシドを含み、2-ヒドロキシベンゾフェノン骨格を有する紫外線吸収剤としてオキシベンゼン-4、オキシベンゼン-3又はオキシベンゼン-1を含み、第1剤の全質量に対して0.5質量%~10質量%の炭酸水素アンモニウムを更に含み、第1剤の全質量に対して1質量%~12質量%のベンジルアルコールを更に含み、酸化防止剤として亜硫酸ナトリウムを更に含む場合を挙げることができる。
As a particularly preferred example of the first agent in the hair dye of the present invention, a substance that develops color by reacting with iron, a combination of tannic acid and salicylic acid or a salicylic acid derivative, or pyrogallol and gallic acid or a derivative thereof As a compound represented by the formula 1, which includes a combination, polyoxyethylene methyl glucoside having an addition mole number of polyoxyethylene of 10 or 20, or polyoxypropylene methyl glucoside having an addition mole number of polyoxypropylene of 10 or 20 And an oxybenzene-4, oxybenzene-3 or oxybenzene-1 as an ultraviolet absorber having a 2-hydroxybenzophenone skeleton, and 0.5 wt% to 10 wt% with respect to the total weight of the first agent Further containing ammonium hydrogen carbonate, 1% by mass relative to the total mass of the first agent Further comprising a 12 weight percent benzyl alcohol, can be mentioned may further comprise sodium sulfite as an antioxidant.
<第2剤>
本発明の染毛剤における第2剤は、鉄塩を含む。
本発明で用いる鉄塩としては、染毛作用を発揮できるものであれば特に限定されないが、一般的には、硫酸第一鉄、塩化第一鉄、酢酸第一鉄、硫酸第二鉄、塩化第二鉄、酢酸第二鉄などを使用することができる、上記の中でも好ましくは、硫酸第一鉄、又は塩化第二鉄である。
鉄塩の使用量は、本発明の効果が得られる限り特に限定されないが、好ましくは第2剤の全質量に対して0.5~10質量%であり、好ましくは1~6質量%である。 <Second agent>
The second agent in the hair dye of the present invention contains an iron salt.
The iron salt used in the present invention is not particularly limited as long as it can exhibit a hair dyeing action, but in general, ferrous sulfate, ferrous chloride, ferrous acetate, ferric sulfate, chloride Of these, ferric sulfate or ferric chloride can be used. Ferric sulfate, ferric acetate and the like can be used.
The amount of iron salt used is not particularly limited as long as the effect of the present invention is obtained, but it is preferably 0.5 to 10% by mass, preferably 1 to 6% by mass with respect to the total mass of the second agent. .
本発明の染毛剤における第2剤は、鉄塩を含む。
本発明で用いる鉄塩としては、染毛作用を発揮できるものであれば特に限定されないが、一般的には、硫酸第一鉄、塩化第一鉄、酢酸第一鉄、硫酸第二鉄、塩化第二鉄、酢酸第二鉄などを使用することができる、上記の中でも好ましくは、硫酸第一鉄、又は塩化第二鉄である。
鉄塩の使用量は、本発明の効果が得られる限り特に限定されないが、好ましくは第2剤の全質量に対して0.5~10質量%であり、好ましくは1~6質量%である。 <Second agent>
The second agent in the hair dye of the present invention contains an iron salt.
The iron salt used in the present invention is not particularly limited as long as it can exhibit a hair dyeing action, but in general, ferrous sulfate, ferrous chloride, ferrous acetate, ferric sulfate, chloride Of these, ferric sulfate or ferric chloride can be used. Ferric sulfate, ferric acetate and the like can be used.
The amount of iron salt used is not particularly limited as long as the effect of the present invention is obtained, but it is preferably 0.5 to 10% by mass, preferably 1 to 6% by mass with respect to the total mass of the second agent. .
第2剤は、鉄塩の他に、第1剤で説明した酸化防止剤をさらに含んでいてもよい。
第2剤においては、酸化防止剤のうち、L-アスコルビン酸及びその塩から選択される1種以上を含有することがより好ましい。L-アスコルビン酸の塩としては、L-アスコルビン酸ナトリウム、L-アスコルビン酸カルシウム等が挙げられる。
第2剤において、酸化防止剤は、いずれかを1種単独で使用してもよく、2種以上を併用してもよい。
第2剤が酸化防止剤を含む場合、その含有量は特に限定されないが、第2剤の全質量に対して、0.5質量%~10質量%含有してもよく、1質量%~6質量%含有することがより好ましい。 The second agent may further contain the antioxidant described in the first agent in addition to the iron salt.
More preferably, the second agent contains at least one selected from L-ascorbic acid and salts thereof among the antioxidants. Examples of the salt of L-ascorbic acid include sodium L-ascorbate and calcium L-ascorbate.
In the second agent, any one of the antioxidants may be used alone, or two or more may be used in combination.
When the second agent contains an antioxidant, the content thereof is not particularly limited, but may be 0.5% by mass to 10% by mass with respect to the total mass of the second agent, and may be 1% by mass to 6%. It is more preferable to contain by mass.
第2剤においては、酸化防止剤のうち、L-アスコルビン酸及びその塩から選択される1種以上を含有することがより好ましい。L-アスコルビン酸の塩としては、L-アスコルビン酸ナトリウム、L-アスコルビン酸カルシウム等が挙げられる。
第2剤において、酸化防止剤は、いずれかを1種単独で使用してもよく、2種以上を併用してもよい。
第2剤が酸化防止剤を含む場合、その含有量は特に限定されないが、第2剤の全質量に対して、0.5質量%~10質量%含有してもよく、1質量%~6質量%含有することがより好ましい。 The second agent may further contain the antioxidant described in the first agent in addition to the iron salt.
More preferably, the second agent contains at least one selected from L-ascorbic acid and salts thereof among the antioxidants. Examples of the salt of L-ascorbic acid include sodium L-ascorbate and calcium L-ascorbate.
In the second agent, any one of the antioxidants may be used alone, or two or more may be used in combination.
When the second agent contains an antioxidant, the content thereof is not particularly limited, but may be 0.5% by mass to 10% by mass with respect to the total mass of the second agent, and may be 1% by mass to 6%. It is more preferable to contain by mass.
<他の成分>
第1剤及び/又は第2剤には、上記各成分に加えて各種の成分を加えてもよい。
他の成分としては、基剤、界面活性剤、溶剤、pH調整剤、湿潤剤、増粘剤、防腐剤、油脂類、有機酸、香料、金属臭のマスキング剤、着色剤、等などが挙げられる。また、他の成分としては、本発明の目的を損なわない範囲で通常の化粧品等に用いられる成分、例えば、育毛養毛剤、フケ防止剤、抗菌剤、柔軟剤、保湿剤、活性酸素除去剤、抗微生物剤、シリコーン、ミネラル、加水分解タンパク、ペプチド、アミノ酸類を適宜配合することもできる。これらの他の成分の含有量は、本発明の効果を奏する範囲内で適宜設定することができる。 <Other ingredients>
In addition to the above components, various components may be added to the first agent and / or the second agent.
Other components include bases, surfactants, solvents, pH adjusters, wetting agents, thickeners, preservatives, fats and oils, organic acids, fragrances, metal odor masking agents, colorants, and the like. It is done. In addition, as other components, components that are used in ordinary cosmetics and the like within a range not impairing the object of the present invention, such as hair restoration agents, anti-dandruff agents, antibacterial agents, softeners, moisturizers, active oxygen removers, anti-oxidants, Microbial agents, silicones, minerals, hydrolyzed proteins, peptides, and amino acids can be appropriately blended. The content of these other components can be appropriately set within the range where the effects of the present invention are exhibited.
第1剤及び/又は第2剤には、上記各成分に加えて各種の成分を加えてもよい。
他の成分としては、基剤、界面活性剤、溶剤、pH調整剤、湿潤剤、増粘剤、防腐剤、油脂類、有機酸、香料、金属臭のマスキング剤、着色剤、等などが挙げられる。また、他の成分としては、本発明の目的を損なわない範囲で通常の化粧品等に用いられる成分、例えば、育毛養毛剤、フケ防止剤、抗菌剤、柔軟剤、保湿剤、活性酸素除去剤、抗微生物剤、シリコーン、ミネラル、加水分解タンパク、ペプチド、アミノ酸類を適宜配合することもできる。これらの他の成分の含有量は、本発明の効果を奏する範囲内で適宜設定することができる。 <Other ingredients>
In addition to the above components, various components may be added to the first agent and / or the second agent.
Other components include bases, surfactants, solvents, pH adjusters, wetting agents, thickeners, preservatives, fats and oils, organic acids, fragrances, metal odor masking agents, colorants, and the like. It is done. In addition, as other components, components that are used in ordinary cosmetics and the like within a range not impairing the object of the present invention, such as hair restoration agents, anti-dandruff agents, antibacterial agents, softeners, moisturizers, active oxygen removers, anti-oxidants, Microbial agents, silicones, minerals, hydrolyzed proteins, peptides, and amino acids can be appropriately blended. The content of these other components can be appropriately set within the range where the effects of the present invention are exhibited.
基剤としては、高級アルコール類、炭化水素、脂肪酸エステル、植物油、脂肪酸等を挙げることができる。
界面活性剤としては、ポリオキシエチレンアルキルエーテル、ポリオキシエチレン、ポリオキシプロピレンアルキルエーテル、グリセリン脂肪酸エステル、ポリグリセリン脂肪酸エステル、ポリエチレングリコール脂肪酸エステル、ポリオキシエチレンアルキルエーテルリン酸及びその塩、アルキルグルコシド、N-アシルアミノ酸塩、アルキルエーテルカルボン酸塩、アルキル硫酸塩、ポリオキシエチレンアルキルエーテル硫酸塩、スルホン酸塩、アルキルアンモニウム塩、アルキルアミドプロピルベタイン等を挙げることができる。 Examples of the base include higher alcohols, hydrocarbons, fatty acid esters, vegetable oils, fatty acids and the like.
As the surfactant, polyoxyethylene alkyl ether, polyoxyethylene, polyoxypropylene alkyl ether, glycerin fatty acid ester, polyglycerin fatty acid ester, polyethylene glycol fatty acid ester, polyoxyethylene alkyl ether phosphoric acid and its salt, alkyl glucoside, Examples thereof include N-acyl amino acid salts, alkyl ether carboxylates, alkyl sulfates, polyoxyethylene alkyl ether sulfates, sulfonates, alkyl ammonium salts, and alkylamidopropyl betaines.
界面活性剤としては、ポリオキシエチレンアルキルエーテル、ポリオキシエチレン、ポリオキシプロピレンアルキルエーテル、グリセリン脂肪酸エステル、ポリグリセリン脂肪酸エステル、ポリエチレングリコール脂肪酸エステル、ポリオキシエチレンアルキルエーテルリン酸及びその塩、アルキルグルコシド、N-アシルアミノ酸塩、アルキルエーテルカルボン酸塩、アルキル硫酸塩、ポリオキシエチレンアルキルエーテル硫酸塩、スルホン酸塩、アルキルアンモニウム塩、アルキルアミドプロピルベタイン等を挙げることができる。 Examples of the base include higher alcohols, hydrocarbons, fatty acid esters, vegetable oils, fatty acids and the like.
As the surfactant, polyoxyethylene alkyl ether, polyoxyethylene, polyoxypropylene alkyl ether, glycerin fatty acid ester, polyglycerin fatty acid ester, polyethylene glycol fatty acid ester, polyoxyethylene alkyl ether phosphoric acid and its salt, alkyl glucoside, Examples thereof include N-acyl amino acid salts, alkyl ether carboxylates, alkyl sulfates, polyoxyethylene alkyl ether sulfates, sulfonates, alkyl ammonium salts, and alkylamidopropyl betaines.
溶剤としては、水、エタノール、イソプロピルアルコール、ベンジルアルコール、1,3-ブチレングリコール、2-メチル-2,4-ペンタンジオール、グリセリン、プロピレングリコール等を挙げることができる。
pH調整剤としては、アンモニア、炭酸アンモニウム、水酸化カリウム、水酸化ナトリウム、モノエタノールアミン、イソプロパノールアミン、塩酸等を用いることができる。 Examples of the solvent include water, ethanol, isopropyl alcohol, benzyl alcohol, 1,3-butylene glycol, 2-methyl-2,4-pentanediol, glycerin, propylene glycol and the like.
As the pH adjuster, ammonia, ammonium carbonate, potassium hydroxide, sodium hydroxide, monoethanolamine, isopropanolamine, hydrochloric acid and the like can be used.
pH調整剤としては、アンモニア、炭酸アンモニウム、水酸化カリウム、水酸化ナトリウム、モノエタノールアミン、イソプロパノールアミン、塩酸等を用いることができる。 Examples of the solvent include water, ethanol, isopropyl alcohol, benzyl alcohol, 1,3-butylene glycol, 2-methyl-2,4-pentanediol, glycerin, propylene glycol and the like.
As the pH adjuster, ammonia, ammonium carbonate, potassium hydroxide, sodium hydroxide, monoethanolamine, isopropanolamine, hydrochloric acid and the like can be used.
湿潤剤としては、プロピレングリコール、グリセリン、ソルビトール、ピロリドンカルボン酸ナトリウム、アミノ酸、植物油等を挙げることができる。
増粘剤としては、例えば、キサンタンガム、アクリル酸・メタクリル酸アルキル共重合体、ポリエチレングリコール、ヒドロキシエチルセルロース等を挙げることができる。中でも、好適な増粘剤の一つとして、キサンタンガムを用いることが好ましい。キサンタンガムは、キサントモナス属菌を用いて炭水化物を醗酵させて得られた多糖類である。 Examples of the wetting agent include propylene glycol, glycerin, sorbitol, sodium pyrrolidone carboxylate, amino acids, vegetable oils and the like.
Examples of the thickener include xanthan gum, acrylic acid / alkyl methacrylate copolymer, polyethylene glycol, and hydroxyethyl cellulose. Of these, xanthan gum is preferably used as one of the preferred thickeners. Xanthan gum is a polysaccharide obtained by fermenting carbohydrates using Xanthomonas sp.
増粘剤としては、例えば、キサンタンガム、アクリル酸・メタクリル酸アルキル共重合体、ポリエチレングリコール、ヒドロキシエチルセルロース等を挙げることができる。中でも、好適な増粘剤の一つとして、キサンタンガムを用いることが好ましい。キサンタンガムは、キサントモナス属菌を用いて炭水化物を醗酵させて得られた多糖類である。 Examples of the wetting agent include propylene glycol, glycerin, sorbitol, sodium pyrrolidone carboxylate, amino acids, vegetable oils and the like.
Examples of the thickener include xanthan gum, acrylic acid / alkyl methacrylate copolymer, polyethylene glycol, and hydroxyethyl cellulose. Of these, xanthan gum is preferably used as one of the preferred thickeners. Xanthan gum is a polysaccharide obtained by fermenting carbohydrates using Xanthomonas sp.
<染毛剤の構成>
本発明の染毛剤は、第1剤及び第2剤を含むものである。
第1剤と第2剤との割合(第1剤:第2剤)は、質量比で1:0.5~1:2の範囲が好ましく、1:0.8~1:1.2の範囲がより好ましく、1:1がさらに好ましい。
第1剤のpHは、好ましくはpH5~10であり、より好ましくはpH6~9である。
第2剤のpHは、好ましくはpH2~6であり、より好ましくはpH3~5である。 <Composition of hair dye>
The hair dye of the present invention contains a first agent and a second agent.
The ratio of the first agent to the second agent (first agent: second agent) is preferably in the range of 1: 0.5 to 1: 2 by mass ratio, and is 1: 0.8 to 1: 1.2. The range is more preferable, and 1: 1 is more preferable.
The pH of the first agent is preferably pH 5 to 10, more preferably pH 6 to 9.
The pH of the second agent is preferably pH 2-6, more preferably pH 3-5.
本発明の染毛剤は、第1剤及び第2剤を含むものである。
第1剤と第2剤との割合(第1剤:第2剤)は、質量比で1:0.5~1:2の範囲が好ましく、1:0.8~1:1.2の範囲がより好ましく、1:1がさらに好ましい。
第1剤のpHは、好ましくはpH5~10であり、より好ましくはpH6~9である。
第2剤のpHは、好ましくはpH2~6であり、より好ましくはpH3~5である。 <Composition of hair dye>
The hair dye of the present invention contains a first agent and a second agent.
The ratio of the first agent to the second agent (first agent: second agent) is preferably in the range of 1: 0.5 to 1: 2 by mass ratio, and is 1: 0.8 to 1: 1.2. The range is more preferable, and 1: 1 is more preferable.
The pH of the first agent is preferably pH 5 to 10, more preferably pH 6 to 9.
The pH of the second agent is preferably pH 2-6, more preferably pH 3-5.
第1剤及び第2剤の剤型は、特に制限されない。例えば、クリーム、液体、ゲル、エマルション、スプレー剤、エアゾール型等とすることができる。中でも、エアゾール型が好ましい。なお、第1剤の剤型と第2剤の剤型とは、同一であっても、異なっていてもよい。
第1剤及び第2剤は、各剤型の種類に従い選択できる製剤化に必要な公知の成分をさらに含有することができる。 The dosage form of the first agent and the second agent is not particularly limited. For example, it can be a cream, liquid, gel, emulsion, spray, aerosol type or the like. Of these, the aerosol type is preferable. The dosage form of the first agent and the dosage form of the second agent may be the same or different.
The 1st agent and the 2nd agent can further contain a publicly known ingredient required for formulation which can be chosen according to the kind of each dosage form.
第1剤及び第2剤は、各剤型の種類に従い選択できる製剤化に必要な公知の成分をさらに含有することができる。 The dosage form of the first agent and the second agent is not particularly limited. For example, it can be a cream, liquid, gel, emulsion, spray, aerosol type or the like. Of these, the aerosol type is preferable. The dosage form of the first agent and the dosage form of the second agent may be the same or different.
The 1st agent and the 2nd agent can further contain a publicly known ingredient required for formulation which can be chosen according to the kind of each dosage form.
製剤化に必要な公知の成分としては、剤型の種類ごとに適宜設定すればよい。
エアゾール型剤型を例に挙げれば、第1剤又は第2剤と、圧縮ガス、界面活性剤、増粘剤及び/又は液化ガス等とを、嫌気雰囲気下で耐圧容器に充填することにより製造することができる。なお、ここで用いられる圧縮ガスとしては、窒素、炭酸、アルゴンなどが好ましい。その他の剤型についても、公知の方法に従い調製することができる。 What is necessary is just to set suitably as a well-known component required for formulation for every kind of dosage form.
Taking an aerosol-type dosage form as an example, it is manufactured by filling a pressure-resistant container with a first agent or a second agent and a compressed gas, a surfactant, a thickener and / or a liquefied gas in an anaerobic atmosphere. can do. The compressed gas used here is preferably nitrogen, carbonic acid, argon or the like. Other dosage forms can also be prepared according to known methods.
エアゾール型剤型を例に挙げれば、第1剤又は第2剤と、圧縮ガス、界面活性剤、増粘剤及び/又は液化ガス等とを、嫌気雰囲気下で耐圧容器に充填することにより製造することができる。なお、ここで用いられる圧縮ガスとしては、窒素、炭酸、アルゴンなどが好ましい。その他の剤型についても、公知の方法に従い調製することができる。 What is necessary is just to set suitably as a well-known component required for formulation for every kind of dosage form.
Taking an aerosol-type dosage form as an example, it is manufactured by filling a pressure-resistant container with a first agent or a second agent and a compressed gas, a surfactant, a thickener and / or a liquefied gas in an anaerobic atmosphere. can do. The compressed gas used here is preferably nitrogen, carbonic acid, argon or the like. Other dosage forms can also be prepared according to known methods.
[染毛方法]
本発明の毛髪の染毛方法は、本発明の第1剤と第2剤とを含む染毛剤を毛髪に付与することを含む。なお、第1剤及び第2剤については、前述した事項をそのまま適用することができる。
毛髪としては、特に頭髪が挙げられる。 [Hair dyeing method]
The hair coloring method of the present invention includes applying a hair dye containing the first agent and the second agent of the present invention to hair. In addition, about the 1st agent and the 2nd agent, the matter mentioned above is applicable as it is.
Examples of hair include scalp hair.
本発明の毛髪の染毛方法は、本発明の第1剤と第2剤とを含む染毛剤を毛髪に付与することを含む。なお、第1剤及び第2剤については、前述した事項をそのまま適用することができる。
毛髪としては、特に頭髪が挙げられる。 [Hair dyeing method]
The hair coloring method of the present invention includes applying a hair dye containing the first agent and the second agent of the present invention to hair. In addition, about the 1st agent and the 2nd agent, the matter mentioned above is applicable as it is.
Examples of hair include scalp hair.
毛髪に付与する方法としては、第1剤を毛髪に付与し、一定時間放置し、その後第2剤を毛髪に付与し、一定時間放置し、上記第1剤及び上記第2剤を洗い流す方法が挙げられる。また、毛髪に付与する別の方法としては、第1剤及び第2剤を同時に毛髪に付与し、一定時間放置し、上記第1剤及び上記第2剤を洗い流す方法が挙げられる。
As a method for applying to the hair, there is a method in which the first agent is applied to the hair and allowed to stand for a certain period of time, and then the second agent is applied to the hair and left to stand for a certain period of time to wash away the first and second agents. Can be mentioned. Further, as another method for applying to the hair, there may be mentioned a method in which the first agent and the second agent are simultaneously applied to the hair, left for a certain period of time, and the first agent and the second agent are washed away.
毛髪への付与は、公知の方法に従い行うことができる。具体的には、直接毛髪に付与してもよく、手又はブラシなどの道具を使って毛髪に塗布してもよい。剤の飛び散りや液ダレを防止する観点から、手袋をした手を用いて毛髪に塗布することがより好ましい。
第1剤及び第2剤を放置する時間は適宜設定することができる。また、第1剤及び第2剤を洗い流す方法は、公知の方法を用いればよい。 The application to hair can be performed according to a known method. Specifically, it may be applied directly to the hair or may be applied to the hair using a tool such as a hand or a brush. From the viewpoint of preventing the agent from splashing and dripping, it is more preferable to apply it to the hair using a gloved hand.
The time for leaving the first agent and the second agent can be set as appropriate. Moreover, what is necessary is just to use a well-known method for the method of washing away the 1st agent and the 2nd agent.
第1剤及び第2剤を放置する時間は適宜設定することができる。また、第1剤及び第2剤を洗い流す方法は、公知の方法を用いればよい。 The application to hair can be performed according to a known method. Specifically, it may be applied directly to the hair or may be applied to the hair using a tool such as a hand or a brush. From the viewpoint of preventing the agent from splashing and dripping, it is more preferable to apply it to the hair using a gloved hand.
The time for leaving the first agent and the second agent can be set as appropriate. Moreover, what is necessary is just to use a well-known method for the method of washing away the 1st agent and the 2nd agent.
染毛剤の付与量としては、適宜設定することができる。例えば、長さ20センチ程度の頭髪に、第1剤を30g~70g程度、第2剤を30g~70g程度付与することが好ましい。また、第1剤を40g~60g程度、第2剤を40g~60g程度付与することがさらに好ましく、一例としては、第1剤を50g及び第2剤を50g付与することができる。
The amount of hair dye applied can be appropriately set. For example, it is preferable to apply about 30 g to 70 g of the first agent and about 30 g to 70 g of the second agent to hair having a length of about 20 cm. Further, it is more preferable to apply about 40 g to 60 g of the first agent and about 40 g to 60 g of the second agent. As an example, 50 g of the first agent and 50 g of the second agent can be applied.
以下に、本発明の実施例を挙げて本発明をさらに具体的に説明する。なお、以下の実施例に示される材料、使用量、割合、処理内容、処理手順等は、本発明の趣旨を逸脱しない限り適宜変更することができる。したがって、本発明の範囲は以下に示す具体例により限定的に解釈されるべきものではない。
Hereinafter, the present invention will be described in more detail with reference to examples of the present invention. In addition, the material, usage-amount, ratio, processing content, processing procedure, etc. which are shown in the following Examples can be changed suitably unless it deviates from the meaning of this invention. Therefore, the scope of the present invention should not be construed as being limited by the specific examples shown below.
(染毛剤の調製)
下記の表1に示す組成の第1剤、及び下記の表2に示す組成の第2剤を常法により製造した。各化合物についての表中の数値は、第1剤又第2剤のそれぞれの全質量に対する質量%を示す。なお、表1中の水酸化ナトリウムにおける適量は、pH7に調整するのに必要な量を意味する。 (Preparation of hair dye)
The 1st agent of the composition shown in the following Table 1 and the 2nd agent of the composition shown in the following Table 2 were manufactured by a conventional method. The numerical value in the table | surface about each compound shows the mass% with respect to each total mass of the 1st agent or the 2nd agent. The appropriate amount of sodium hydroxide in Table 1 means the amount necessary to adjust to pH 7.
下記の表1に示す組成の第1剤、及び下記の表2に示す組成の第2剤を常法により製造した。各化合物についての表中の数値は、第1剤又第2剤のそれぞれの全質量に対する質量%を示す。なお、表1中の水酸化ナトリウムにおける適量は、pH7に調整するのに必要な量を意味する。 (Preparation of hair dye)
The 1st agent of the composition shown in the following Table 1 and the 2nd agent of the composition shown in the following Table 2 were manufactured by a conventional method. The numerical value in the table | surface about each compound shows the mass% with respect to each total mass of the 1st agent or the 2nd agent. The appropriate amount of sodium hydroxide in Table 1 means the amount necessary to adjust to pH 7.
(染毛方法)
長さ約10センチの白髪(品番:BS-C、ビューラックス社製)毛束1gに、第1剤各2gを塗布し、均一にのばした後、20分間放置後、第2剤各2gを塗布し、均一にのばした後、10分間放置した。その後、シャンプー及びリンス処理し、ドライヤーで毛束を乾燥させた。 (Hair dyeing method)
Apply 1g each of the first agent to 1g of white hair (product number: BS-C, manufactured by Beaulux) about 10 cm long, spread it uniformly, leave it for 20 minutes, and then 2g each of the second agent Was applied, spread evenly, and allowed to stand for 10 minutes. Thereafter, shampooing and rinsing were performed, and the hair bundle was dried with a dryer.
長さ約10センチの白髪(品番:BS-C、ビューラックス社製)毛束1gに、第1剤各2gを塗布し、均一にのばした後、20分間放置後、第2剤各2gを塗布し、均一にのばした後、10分間放置した。その後、シャンプー及びリンス処理し、ドライヤーで毛束を乾燥させた。 (Hair dyeing method)
Apply 1g each of the first agent to 1g of white hair (product number: BS-C, manufactured by Beaulux) about 10 cm long, spread it uniformly, leave it for 20 minutes, and then 2g each of the second agent Was applied, spread evenly, and allowed to stand for 10 minutes. Thereafter, shampooing and rinsing were performed, and the hair bundle was dried with a dryer.
(染毛性の評価)
染毛した毛束をミノルタ社製のCR200型色彩色差計で測色し、染毛前の元の白髪とのΔL値から、下記基準で評価した。なお、ΔL値とは、染毛前の毛束と染毛後の毛束について、色彩色差計で測定した値の差のことである。
A:ΔL値≦25(染毛力が非常に強い)
B:25<ΔL値≦30(染毛力が強い)
C:30<ΔL値(染毛力が弱い) (Evaluation of hair dyeing properties)
The hair bundle that was dyed was measured with a CR200 color difference meter manufactured by Minolta, and evaluated based on the following criteria from the ΔL value with the original white hair before dyeing. The ΔL value is the difference between values measured with a color difference meter for the hair bundle before dyeing and the hair bundle after dyeing.
A: ΔL value ≦ 25 (the hair dyeing power is very strong)
B: 25 <ΔL value ≦ 30 (strong hair dyeing power)
C: 30 <ΔL value (weak hair dyeing power)
染毛した毛束をミノルタ社製のCR200型色彩色差計で測色し、染毛前の元の白髪とのΔL値から、下記基準で評価した。なお、ΔL値とは、染毛前の毛束と染毛後の毛束について、色彩色差計で測定した値の差のことである。
A:ΔL値≦25(染毛力が非常に強い)
B:25<ΔL値≦30(染毛力が強い)
C:30<ΔL値(染毛力が弱い) (Evaluation of hair dyeing properties)
The hair bundle that was dyed was measured with a CR200 color difference meter manufactured by Minolta, and evaluated based on the following criteria from the ΔL value with the original white hair before dyeing. The ΔL value is the difference between values measured with a color difference meter for the hair bundle before dyeing and the hair bundle after dyeing.
A: ΔL value ≦ 25 (the hair dyeing power is very strong)
B: 25 <ΔL value ≦ 30 (strong hair dyeing power)
C: 30 <ΔL value (weak hair dyeing power)
(皮膚着色性の評価)
実施例及び比較例の第1剤をパネラーの前腕内側に直径1cmの円状範囲に薄く塗り、20分間放置した後、第2剤を重ねて塗布し、10分間放置した後、温水で洗い流した。さらにシャンプーを使用して1分間指で軽くこすり、温水で洗い流した後、皮膚への染着の度合いを下記の基準により評価した。
A:地肌汚れが殆どない
B:地肌汚れが少ない
C:地肌汚れがある (Evaluation of skin color)
The first agent of Examples and Comparative Examples was thinly applied in a circular area with a diameter of 1 cm on the inner side of the forearm of the paneler, allowed to stand for 20 minutes, then the second agent was applied again, allowed to stand for 10 minutes, and then rinsed with warm water. . Furthermore, after lightly rubbing with a finger for 1 minute using a shampoo and washing away with warm water, the degree of dyeing on the skin was evaluated according to the following criteria.
A: There is almost no background dirt B: There is little background dirt C: There is background dirt
実施例及び比較例の第1剤をパネラーの前腕内側に直径1cmの円状範囲に薄く塗り、20分間放置した後、第2剤を重ねて塗布し、10分間放置した後、温水で洗い流した。さらにシャンプーを使用して1分間指で軽くこすり、温水で洗い流した後、皮膚への染着の度合いを下記の基準により評価した。
A:地肌汚れが殆どない
B:地肌汚れが少ない
C:地肌汚れがある (Evaluation of skin color)
The first agent of Examples and Comparative Examples was thinly applied in a circular area with a diameter of 1 cm on the inner side of the forearm of the paneler, allowed to stand for 20 minutes, then the second agent was applied again, allowed to stand for 10 minutes, and then rinsed with warm water. . Furthermore, after lightly rubbing with a finger for 1 minute using a shampoo and washing away with warm water, the degree of dyeing on the skin was evaluated according to the following criteria.
A: There is almost no background dirt B: There is little background dirt C: There is background dirt
(保存安定性の評価)
4℃で1ヵ月保管品と、50℃で1ヵ月経時品を用い、上記染毛方法で染毛した毛束をミノルタ社製のCR200型色彩色差計で測色し、その色差(ΔE値)から、下記基準で評価した。なお、ΔE値とは、4℃保管品と50℃で1カ月経時品とについて、色彩色差計で測定した値の差のことである。
A:ΔE≦2(目視で殆ど差がわからない)
B:2<ΔE<4(目視で若干差がわかる)
C:4≦ΔE(目視で差がわかる) (Evaluation of storage stability)
Using a product stored for 1 month at 4 ° C. and a product aged for 1 month at 50 ° C., the hair bundle dyed by the above-mentioned hair dyeing method is measured with a CR200 type color difference meter manufactured by Minolta, and the color difference (ΔE value). From the evaluation, the following criteria were used. The ΔE value is a difference between values measured with a color difference meter between a product stored at 4 ° C. and a product aged at 50 ° C. for one month.
A: ΔE ≦ 2 (mostly no difference is visible)
B: 2 <ΔE <4 (a slight difference can be visually observed)
C: 4 ≦ ΔE (a difference can be visually confirmed)
4℃で1ヵ月保管品と、50℃で1ヵ月経時品を用い、上記染毛方法で染毛した毛束をミノルタ社製のCR200型色彩色差計で測色し、その色差(ΔE値)から、下記基準で評価した。なお、ΔE値とは、4℃保管品と50℃で1カ月経時品とについて、色彩色差計で測定した値の差のことである。
A:ΔE≦2(目視で殆ど差がわからない)
B:2<ΔE<4(目視で若干差がわかる)
C:4≦ΔE(目視で差がわかる) (Evaluation of storage stability)
Using a product stored for 1 month at 4 ° C. and a product aged for 1 month at 50 ° C., the hair bundle dyed by the above-mentioned hair dyeing method is measured with a CR200 type color difference meter manufactured by Minolta, and the color difference (ΔE value). From the evaluation, the following criteria were used. The ΔE value is a difference between values measured with a color difference meter between a product stored at 4 ° C. and a product aged at 50 ° C. for one month.
A: ΔE ≦ 2 (mostly no difference is visible)
B: 2 <ΔE <4 (a slight difference can be visually observed)
C: 4 ≦ ΔE (a difference can be visually confirmed)
上記の評価の結果を表1に記載する。
実施例1~8の染毛剤を用いた場合には、染毛性及び皮膚着色性はA又はBであり共に良好であった。一方、親水性基を有するメチルグルコシド誘導体を使用しない比較例1、3及び4では皮膚着色性の評価がCであり、実施例より劣っている。また、ベタインを使用した比較例2においては染毛性の評価がCであり、実施例より劣っている。また、実施例1~8の染毛剤は、保存安定性の評価が全てAであり優れていた。 The results of the above evaluation are listed in Table 1.
When the hair dyes of Examples 1 to 8 were used, the hair dyeability and skin colorability were either A or B, both being good. On the other hand, in Comparative Examples 1, 3 and 4 in which a methylglucoside derivative having a hydrophilic group is not used, the evaluation of skin colorability is C, which is inferior to the examples. Moreover, in the comparative example 2 which uses betaine, evaluation of hair dyeing property is C, and is inferior to an Example. In addition, the hair dyes of Examples 1 to 8 were all excellent in storage stability evaluation A.
実施例1~8の染毛剤を用いた場合には、染毛性及び皮膚着色性はA又はBであり共に良好であった。一方、親水性基を有するメチルグルコシド誘導体を使用しない比較例1、3及び4では皮膚着色性の評価がCであり、実施例より劣っている。また、ベタインを使用した比較例2においては染毛性の評価がCであり、実施例より劣っている。また、実施例1~8の染毛剤は、保存安定性の評価が全てAであり優れていた。 The results of the above evaluation are listed in Table 1.
When the hair dyes of Examples 1 to 8 were used, the hair dyeability and skin colorability were either A or B, both being good. On the other hand, in Comparative Examples 1, 3 and 4 in which a methylglucoside derivative having a hydrophilic group is not used, the evaluation of skin colorability is C, which is inferior to the examples. Moreover, in the comparative example 2 which uses betaine, evaluation of hair dyeing property is C, and is inferior to an Example. In addition, the hair dyes of Examples 1 to 8 were all excellent in storage stability evaluation A.
本発明の染毛剤及び染毛方法は、安全性、染毛性及び保存安定性に優れ、かつ皮膚着色が少ない染毛剤として利用可能である。
The hair dye and hair dyeing method of the present invention can be used as a hair dye excellent in safety, hair dyeability and storage stability, and having little skin coloring.
Claims (13)
- 鉄と反応して発色する物質、及び第1剤の全質量に対して0.1質量%~12質量%の下記式1で示される化合物を含む第1剤;並びに
鉄塩を含む第2剤;
を含む染毛剤。
Hair dye containing.
- 親水性基が、ポリオキシアルキレン基である、請求項1に記載の染毛剤。 The hair dye according to claim 1, wherein the hydrophilic group is a polyoxyalkylene group.
- 式1で示される化合物が、下記式1Aで示される化合物である、請求項1又は2に記載の染毛剤。
- 式1で示される化合物が、ポリオキシエチレンの付加モル数が10~20であるポリオキシエチレンメチルグルコシド、あるいはポリオキシプロピレンの付加モル数が10~20であるポリオキシプロピレンメチルグルコシドである、請求項1から3の何れか一項に記載の染毛剤。 The compound represented by Formula 1 is polyoxyethylene methyl glucoside having an addition mole number of polyoxyethylene of 10 to 20, or polyoxypropylene methyl glucoside having an addition mole number of polyoxypropylene of 10 to 20. Item 4. The hair dye according to any one of Items 1 to 3.
- 鉄と反応して発色する物質が、タンニン酸、サリチル酸及びサリチル酸誘導体、ピロガロール、没食子酸およびその誘導体、五倍子、ログウッド、ヘマテイン、カテコール、フタル酸、オイゲノール、イソオイゲノール、ニコチン酸アミド、デヒドロ酢酸、ピリドキシン、エラグ酸、コウジ酸、マルトール、フェルラ酸、ヒノキチオール、ウコンエキス、クルクミン、オウゴンエキス、タマネギエキス、クエルセチン、ルチン、ヘスペレチン、ヘスペリジン、生コーヒー豆抽出物、カフェー酸、クロロゲン酸、チャエキス、カテキン、エピカテキン、シコンエキス、シソエキス、シソニン、ブドウ葉エキス、ブトウエキス、エノシアニン、ラッカイン酸、ラック、コチニール、カルミン酸、エルダーベリー、アカキャベツ、ムラサキイモ、タマリンド、コウリャン、アピゲニニジン、及びルテオリニジンからなる群から選択される少なくとも1種以上である、請求項1から4の何れか一項に記載の染毛剤。 Substances that develop color by reacting with iron are tannic acid, salicylic acid and salicylic acid derivatives, pyrogallol, gallic acid and its derivatives, pentaploid, logwood, hematein, catechol, phthalic acid, eugenol, isoeugenol, nicotinamide, dehydroacetic acid, Pyridoxine, ellagic acid, kojic acid, maltol, ferulic acid, hinokitiol, turmeric extract, curcumin, ogon extract, onion extract, quercetin, rutin, hesperetin, hesperidin, raw coffee bean extract, caffeic acid, chlorogenic acid, cha extract, catechin, Epicatechin, Shikon extract, Perilla extract, Shisonin, Grape leaf extract, Butou extract, Enocyanin, Lacinate, Lac, Cochineal, Carminic acid, Elderberry, Red cabbage, Murasaki potato, Ta Lind, sorghum, Apigeninijin, and at least one member selected from the group consisting of Ruteorinijin, hair dye according to any one of claims 1 to 4.
- 鉄と反応して発色する物質が、タンニン酸と、サリチル酸又はサリチル酸誘導体との組み合わせ、又はピロガロールと、没食子酸又はその誘導体との組み合わせである、請求項1から5の何れか一項に記載の染毛剤。 The substance that develops color by reacting with iron is a combination of tannic acid and salicylic acid or a salicylic acid derivative, or a combination of pyrogallol and gallic acid or a derivative thereof according to any one of claims 1 to 5. Hair dye.
- 第1剤が、2-ヒドロキシベンゾフェノン骨格を有する紫外線吸収剤を更に含む、請求項1から6の何れか一項に記載の染毛剤。 The hair dye according to any one of claims 1 to 6, wherein the first agent further comprises an ultraviolet absorber having a 2-hydroxybenzophenone skeleton.
- 第1剤が、第1剤の全質量に対して0.5質量%~10質量%のアンモニウム塩を更に含む、請求項1から7の何れか一項に記載の染毛剤。 The hair dye according to any one of claims 1 to 7, wherein the first agent further comprises 0.5% by mass to 10% by mass of an ammonium salt based on the total mass of the first agent.
- 第1剤が、第1剤の全質量に対して1質量%~12質量%のベンジルアルコールを更に含む、請求項1から8の何れか一項に記載の染毛剤。 The hair dye according to any one of claims 1 to 8, wherein the first agent further comprises 1% by mass to 12% by mass of benzyl alcohol based on the total mass of the first agent.
- 第1剤が、酸化防止剤を更に含む、請求項1から9の何れか一項に記載の染毛剤。 The hair dye according to any one of claims 1 to 9, wherein the first agent further comprises an antioxidant.
- 第1剤が、鉄と反応して発色する物質として、タンニン酸と、サリチル酸又はサリチル酸誘導体との組み合わせ、又はピロガロールと、没食子酸又はその誘導体との組み合わせを含み、式1で示される化合物として、ポリオキシエチレンの付加モル数が10又は20であるポリオキシエチレンメチルグルコシド、あるいはポリオキシプロピレンの付加モル数が10又は20であるポリオキシプロピレンメチルグルコシドを含み、2-ヒドロキシベンゾフェノン骨格を有する紫外線吸収剤としてオキシベンゼン-4、オキシベンゼン-3又はオキシベンゼン-1を含み、第1剤の全質量に対して0.5質量%~10質量%の炭酸水素アンモニウムを更に含み、第1剤の全質量に対して1質量%~12質量%のベンジルアルコールを更に含み、酸化防止剤として亜硫酸ナトリウムを更に含む、請求項1から10の何れか一項に記載の染毛剤。 The first agent includes a combination of tannic acid and salicylic acid or a salicylic acid derivative, or a combination of pyrogallol and gallic acid or a derivative thereof as a substance that develops color by reacting with iron. UV absorption having a 2-hydroxybenzophenone skeleton, comprising polyoxyethylene methyl glucoside having an addition mole number of polyoxyethylene of 10 or 20, or polyoxypropylene methyl glucoside having an addition mole number of polyoxypropylene of 10 or 20 Oxybenzene-4, oxybenzene-3 or oxybenzene-1 as an agent, further containing 0.5% by mass to 10% by mass of ammonium hydrogen carbonate with respect to the total mass of the first agent, Further containing 1% by mass to 12% by mass of benzyl alcohol based on the mass, and an acid Further comprising, hair dye according to any one of claims 1 10 sodium sulphite as inhibitor.
- 鉄塩が、硫酸第一鉄、塩化第一鉄、酢酸第一鉄、硫酸第二鉄、塩酸第二鉄及び酢酸第二鉄からなる群より選ばれる少なくとも1種である、請求項1から11の何れか一項に記載の染毛剤。 The iron salt is at least one selected from the group consisting of ferrous sulfate, ferrous chloride, ferrous acetate, ferric sulfate, ferric hydrochloride, and ferric acetate. The hair dye as described in any one of these.
- 請求項1から12の何れか一項に記載の染毛剤を毛髪に付与することを含む毛髪の染毛方法。 A hair dyeing method comprising applying the hair dye according to any one of claims 1 to 12 to hair.
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JP2020083823A (en) * | 2018-11-27 | 2020-06-04 | タカラベルモント株式会社 | Hair treatment agent for dyeing or decolorization |
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JP2012171946A (en) * | 2011-02-24 | 2012-09-10 | Seiwa Kasei Co Ltd | Treatment method for hair |
WO2014002670A1 (en) * | 2012-06-27 | 2014-01-03 | 富士フイルム株式会社 | Hair-dye composition |
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- 2014-09-26 JP JP2014196343A patent/JP2016069280A/en active Pending
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JPH07309732A (en) * | 1994-05-17 | 1995-11-28 | Hoyu Co Ltd | Aerosol type hair dye |
JP2001226241A (en) * | 2001-04-26 | 2001-08-21 | Sanei Kagaku Kk | Composition for blending with stain remover and stain remover |
JP2011057627A (en) * | 2009-09-11 | 2011-03-24 | Mandom Corp | Hair-treating agent |
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JP2020083823A (en) * | 2018-11-27 | 2020-06-04 | タカラベルモント株式会社 | Hair treatment agent for dyeing or decolorization |
JP7125752B2 (en) | 2018-11-27 | 2022-08-25 | タカラベルモント株式会社 | Hair treatment agent for dyeing or bleaching |
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