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EP3215114A1 - Coloration capillaire oxydante - Google Patents

Coloration capillaire oxydante

Info

Publication number
EP3215114A1
EP3215114A1 EP15775007.6A EP15775007A EP3215114A1 EP 3215114 A1 EP3215114 A1 EP 3215114A1 EP 15775007 A EP15775007 A EP 15775007A EP 3215114 A1 EP3215114 A1 EP 3215114A1
Authority
EP
European Patent Office
Prior art keywords
agent
dye
hair dye
oxidative hair
hair
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Withdrawn
Application number
EP15775007.6A
Other languages
German (de)
English (en)
Inventor
Akira Matsutani
Masaki Kawai
Shoji Machida
Shoko NAGAFUCHI
Koji Takada
Hiroaki Fukuda
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Henkel AG and Co KGaA
Original Assignee
Henkel AG and Co KGaA
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Henkel AG and Co KGaA filed Critical Henkel AG and Co KGaA
Publication of EP3215114A1 publication Critical patent/EP3215114A1/fr
Withdrawn legal-status Critical Current

Links

Classifications

    • 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
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00—Cosmetics or similar toiletry preparations
    • A61K8/02—Cosmetics or similar toiletry preparations characterised by special physical form
    • A61K8/04—Dispersions; Emulsions
    • A61K8/042—Gels
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00—Cosmetics or similar toiletry preparations
    • A61K8/02—Cosmetics or similar toiletry preparations characterised by special physical form
    • A61K8/04—Dispersions; Emulsions
    • A61K8/06—Emulsions
    • 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
    • A61K8/40—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing nitrogen
    • A61K8/44—Aminocarboxylic acids or derivatives thereof, e.g. aminocarboxylic acids containing sulfur; Salts; Esters or N-acylated 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
    • A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/46—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing sulfur
    • A61K8/463—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing sulfur containing sulfuric acid derivatives, e.g. sodium lauryl sulfate
    • 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
    • A61K8/604—Alkylpolyglycosides; Derivatives thereof, e.g. esters
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K2800/00—Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
    • A61K2800/40—Chemical, physico-chemical or functional or structural properties of particular ingredients
    • A61K2800/59—Mixtures
    • A61K2800/596—Mixtures of surface active compounds

Definitions

  • the present invention relates to an oxidative hair dye capable of sufficiently dyeing hair and particularly white hair, capable of suppressing any dropping of the oxidative hair dye during application thereof to the hair, capable of also suppressing any dropping of the oxidative hair dye from the hair even during the leaving time, and also excellent in the storage stability.
  • a hair dye that is, a so-called two-agent hair dye is used as a dye for hair, wherein the hair dye comprises a first agent comprising an alkaline agent and a second agent comprising an oxidation agent and wherein the first agent and the second agent are mixed immediately before the use of the hair dye (Patent Documents 1 to 4).
  • the hair dye comprises a first agent comprising an alkaline agent and a second agent comprising an oxidation agent and wherein the first agent and the second agent are mixed immediately before the use of the hair dye
  • Patent Documents 1 to 4 In order to sufficiently dye hair, in particular white hair, with the two-agent hair dye, it is necessary to blend a large amount of the oxidation dye in the first agent. The two-agent hair dye can thereby sufficiently dye the hair.
  • the presence of the large amount of oxidation dye in the hair dye may cause an interaction between the oxidation dye and an additive such as a surfactant or a polymer. This interaction leads to some problems such as that the viscos
  • the oxidation dye when the oxidation dye is added in the hair dye in high concentration, an interaction may be generated between the additive such as a surfactant or a polymer, and the oxidation dye. This interaction may cause a decrease of the viscosity of the hair dye and precipitation of sediments in the hair dye over time. As a result, the storage stability may be degraded which is the performance required as an oxidative hair dye. It is also required that the oxidative hair dye should stay on the hair and cause no dropping thereof during the application thereof to the hair.
  • An object of the present invention is to provide an oxidative hair dye excellent in the storage stability since the hair dye is stable over time even when an oxidation dye is blended in the first agent thereof in high concentration, capable of suppressing any dropping of the oxidative hair dye from the hair during the application thereof and during the leaving time after the application thereof, and capable of sufficiently dyeing the hair, in particular white hair.
  • An oxidative hair dye which is used by mixing a first agent comprising an alkaline agent and a second agent comprising an oxidation agent, wherein the first agent comprises 1 to 20% by mass of an oxidation dye based on an overall mass of the first agent, wherein the first agent comprises at least one anionic surfactant, at least one ampholytic surfactant, and at least one alkyl glucoside-type nonionic surfactant, and wherein the oxidative hair dye is in a gel form or an emulsion form.
  • the oxidative hair dye of the present invention hair and particularly white hair can sufficiently be dyed, any dropping of the oxidative hair dye from the hair can be suppressed when the oxidative hair dye is applied to the hair, and any dropping of the oxidative hair dye from the hair can be suppressed even during the leaving time.
  • the first agent is stable over time and the oxidative hair dye of the present invention is therefore excellent in the storage stability.
  • the oxidative hair dye of the present invention comprises a first agent comprising an alkaline agent and a second agent comprising an oxidation agent.
  • the oxidative hair dye of the present invention is a multi-agent oxidative hair dye and is used by mixing at least the first agent and the second agent.
  • the first agent further comprises an oxidation dye in addition to the alkaline agent.
  • the first agent further comprises at least one anionic surfactant, at least one ampholytic surfactant, and at least one alkyl glucoside-type nonionic surfactant.
  • Oxidation dyes are classified into dye intermediates and couplers.
  • the oxidation dye preferably comprises a dye intermediate. These oxidation dyes may be used alone or in combination of two or more of them.
  • the dye intermediates include p-phenylenediamine, toluene-2,5-diamine, N-phenyl-p-phenylenediamine, 4,4'-diaminodiphenylamine, p-aminophenol, o-aminophenol, p-methylaminophenol, N,N-bis(2-hydroxyethyl)-p-phenylenediamine, 2-hydroxyethyl-p-phenylenediamine, o-chlor-p-phenylenediamine, 4-amino-m-cresol, 2-amino-4-hydroxyethylaminoanisole, 2,4-diaminophenol, and the salts thereof.
  • the salts may be hydrochloride salts and sulfate salts.
  • One type of the above may be comprised alone, or two or more types thereof may be comprised in combination as the dye intermediate.
  • the coupler develops its color by bonding with a dye intermediate.
  • the couplers include resorcin, 5-amino-o-cresol, m-aminophenol, 5-(2-hydroxyethylamino)-2-methylphenol, m-phenylenediamine, 2,4-diaminophenoxyethanol, toluene-3,4-diamine, 2,6-diaminopyridine, diphenylamine, N,N-diethyl-m-aminophenol, phenylmethylpyrazolone, and the salts thereof.
  • the salts may be hydrochloride salts and sulfate salts.
  • One type of the above may be comprised alone, or two or more types thereof may be comprised in combination as the coupler.
  • the content of the oxidation dye in the first agent is from 1 to 20% by mass, preferably from 2 to 15% by mass, and more preferably from 3 to 10% by mass, based on an overall mass of the first agent.
  • the hair dyeing property further increases.
  • the content of the oxidation dye in the first agent is equal to or smaller than the upper limit value, the first agent can be established as a stable agent.
  • the oxidation dye may comprise an oxidation dye in the form of a salt. It is said that the oxidation dye in the form of a salt tends to cause problems such as degradation of the storage stability. According to the present invention, however, even when the first agent comprises the oxidation dye in the form of a salt, the oxidative hair dye of the present invention can achieve excellent storage stability.
  • the first agent may further comprise a direct dye.
  • the direct dyes include a nitro dye, an acidic dye, a disperse dye, an HC dye, and a basic dye.
  • the nitro dyes include paranitroorthophenylenediamine, nitroparaphenylenediamine, paranitrometaphenylenediamine sulphate, 2-amino-5-nitrophenol, and picramic acid.
  • the acidic dyes include Blue No. 1 and Acid Orange 7.
  • examples of the disperse dyes include Disperse Violet 1, Disperse Blue 1, and Disperse Black 9.
  • the HC dyes include HC Red 1 and HC Yellow 2.
  • the basic dyes include Basic Blue 99, Basic Brown 16, and Basic Yellow 87.
  • the first agent comprises at least one anionic surfactant, at least one ampholytic surfactant, and at least one alkyl glucoside-type nonionic surfactant.
  • anionic surfactants include a salt of higher fatty acid, a salt of an alkyl sulphuric acid ester, a salt of an alkyl phosphoric acid ester, a salt of an alkyl ether sulfate ester, a salt of an alkyl ether phosphateester, an alkyl ether carboxylate salt, N-acylmethyltauline salt, an alkylsulphosuccinic acid, acyllactate salt, N-acylsarcosine salt, N-acylglutamate salt, and N-acylmethylalanine salt.
  • a salt of an alkyl sulphuric acid ester and a salt of an alkyl ether sulphate ester are preferable.
  • the salt of alkyl sulphuric acid ester is not particularly limited, and the salt thereof comprises an alkyl group of preferably 10 to 22 carbons, and more preferably 10 to 16 carbons.
  • the salt of alkyl ether sulphate ester is not particularly limited, and the salt thereof comprise an alkyl group based on a linear primary alcohol, a linear secondary alcohol, or a branched-chain alcohol of preferably 10 to 20 carbons and more preferably 12 to 14 carbons, and an alkylene oxide group of the salt has an average additional molar number of preferably 0.5 to 5, more preferably 0.5 to 4 and further more preferably 1 to 3.
  • the alkylene oxide may be, for example, ethylene oxide and propylene oxide.
  • the salt thereof is preferably an alkaline metal salt, and examples thereof include a sodium salt and a potassium salt.
  • the use of the anionic surfactant is preferable, from the viewpoint of the foaming property and the stability of the agent.
  • anionic surfactants may be used alone or in combination of two or more of them.
  • the content of the anionic surfactant in the first agent is preferably from 0.1 to 50% by mass, and more preferably from 1 to 20% by mass based on the overall mass of the first agent, from the viewpoint of the foaming property and the stability of the agent.
  • ampholytic surfactants examples include carbobetaine-based, amidebetaine-based, sulfobetaine-based, hydroxysulfobetaine-based, amidesulfobetaine-based, phosphobetaine-based and imidazolinium-based surfactants, each of which comprises an alkyl group, an alkenyl group, or an acyl group, comprising 8 to 24 carbons.
  • the carbobetaine-based surfactants and the sulfobetaine-based surfactants are preferable, from the viewpoint of viscosity.
  • ampholytic surfactants incelude amidopropylbetaine laurate, cocamidopropyl betaine, lauryldimethylaminoacetic acid betaine, and laurylhydroxysulfobetaine. These ampholytic surfactants may be used alone or in combination of two or more of them.
  • the content of the ampholytic surfactant in the first agent is preferably from 0.1 to 50% by mass, and more preferably from 1 to 20% by mass based on the overall mass of the first agent, from the view point of acquiring a proper viscosity.
  • alkyl glucoside-type nonionic surfactants examples include octyl glucodie, nonyl glucoside, decyl glucoside, octyl thioglucoside, lauryl glucoside, and coconut oil alkyl glucoside.
  • the alkyl glucoside-type nonionic surfactant is preferably a C 6 to C 20 -alkyl glucoside, more preferably a C 6 to C 15 -alkyl glucoside, and further more preferably a C 6 to C 12 -alkyl glucoside.
  • the use of these alkyl glucoside-type nonionic surfactants is preferable, from the viewpoint of the foaming property.
  • alkyl glucoside-type nonionic surfactants may be used alone or in combination of two or more of them.
  • the content of the alkyl glucoside-type nonionic surfactant is preferably from 0.1 to 10% by mass, and more preferably from 0.5 to 5% by mass based on the overall mass of the first agent, from the view point of the stability of the agent.
  • the oxidative hair dye of the present invention because the first agent comprises at least one anionic surfactant, at least one ampholytic surfactant, and at least one alkyl glucoside-type nonionic surfactant, the oxidative hair dye comprising the first agent and the second agent can be beaten to be in the form of foam after the oxidative hair dye is applied to the hair.
  • the oxidative hair dye can be caused to evenly adhere to the hair by foaming the oxidative hair dye like shampooing. Therefore, it is possible to make no unevenness of the dyeing hardly occur in the hair after the dyeing.
  • the total content of the surfactants in the first agent is preferably from 5.0 to 50% by mass, and more preferably from 10 to 30% by mass based on the overall mass of the first agent, taking into consideration the dropping and the foaming.
  • the mass ratio of the anionic surfactant and the ampholytic surfactant in the first agent is preferably from 1:3 to 3:1, and more preferably from 1:2 to 2:1.
  • the mass ratio of the anionic surfactant and the ampholytic surfactant in the first agent is within the above range, the oxidative hair dye is excellent particularly in the hair dyeing property and the viscosity can be obtained with which the oxidative hair dye is easily applied.
  • the first agent comprises an alkaline agent.
  • the alkaline agent is not particularly limited. Any conventionally known alkaline agent is usable as the alkaline agent.
  • the alkaline agent may be an inorganic alkaline agent or an organic alkaline agent. These o alkaline agents may be used alone or in combination of two or more of them.
  • alkaline agent examples include ammonia, sodium hydroxide, potassium hydroxide, ammonium carbonate, ammonium bicarbonate, sodium carbonate, isopropanolamine, monoethanolamine, diethanolamine, triethanolamine, and 2-amino-2-methyl-1-propanol.
  • the content of the alkaline agent in the first agent is not particularly limited, and this content can be properly adjusted taking into consideration a desired dyeing property and the like.
  • the content of the alkaline agent in the first agent is preferably from 0.01 to 20% by mass, more preferably from 1 to 15% by mass, and further more preferably from 3 to 10% by mass, based on the overall mass of the first agent.
  • the content of the alkaline agent is equal to or larger than the lower limit value, the dyeing property is particularly enhanced.
  • the content of the alkaline agent is equal to or smaller than the upper limit value, skin stimulation is reduced.
  • the first agent further comprises a reducing agent in addition to the alkaline agent and the oxidation dye.
  • the addition of the reducing agent can suppress development of the color of the oxidation dye when the first agent is exposed to atmosphere.
  • the reducing agents include N-acetyl-L-cysteine, L-ascorbic acid, sodium sulfite, sodium pyrosulfite, thioglycolic acid, and the salts thereof. These reducing agents may be used alone or in combination of two or more of them.
  • the content of the reducing agent in the first agent is preferably from 0 to 2% by mass, and more preferably from 0.01 to 1% by mass based on the overall mass of the first agent, from the viewpoint of improvement of the storage stability.
  • the present invention it is possible to blend other components, which may generally be added to a hair dye, in the first agent, if necessary.
  • the other components which may be added thereto include water soluble cationic polymers such as cationized cellulose and derivatives thereof, cationic starch, cationized guar gum and derivatives thereof, diallyl quarternary ammonium salt/acrylamide copolymer, vinylimidazolium trichloride/vinylpyrolidone copolymer, hydroxyethyl cellulose/dimethyldiallyl ammonium chloride copolymer, vinylpyrolidone/quarternarized dimethylaminoethylmethacrylate copolymer, polyvinylpyrolidone/alkylaminoacrylate copolymer, polyvinylpyrolidone/alkylamino acrylate/vinylcaprolactam copolymer, and vinylpyrolidone/methacrylamidopropyl trimethyl ammonium chloride cop
  • the second agent comprises an oxidation agent.
  • the oxidation agent is not particularly limited, and any conventionally known oxidation agent is usable. These oxidation agents may be used alone or in combination of two or more of them.
  • the oxidation agents are not particularly limited, and examples thereof include hydrogen peroxide, urea hydrogen peroxide, persulfate, perborate, percarbonate, bromate, and periodate.
  • the oxidation agent is preferably hydrogen peroxide, from the view point of further enhancement of the dyeing property.
  • the content of the oxidation agent in the second agent may be properly adjusted.
  • the content of the oxidation agent in the second agent is preferably from 0.01 to 12% by mass, and more preferably from 0.1 to 6% by mass based on the overall mass of the second agent, from the viewpoint of improvement of the dyeing property.
  • the second agent may comprise an anionic polymer as a thickening polymer.
  • the oxidative hair dye of the present invention has more preferable viscosity when the second agent is mixed with the first agent, and there tends to be no dropping of the oxidative hair dye.
  • the anionic polymers include alkyl acrylate/alkyl methacrylate/polyoxyethylenestearyl ether copolymer, alkyl acrylate/polyoxyethylenebeheneth ether methacrylate copolymer, alkyl acrylate/polyoxyethylenecetyl ether itaconate copolymer, and alkyl acrylate/polyoxyethylenestearyl ether methacrylate cross polymer.
  • the content of the anionic polymer in the second agent may be properly adjusted taking into consideration the viscosity and the nature of the oxidative hair dye.
  • the content of the anionic polymer in the second agent is preferably from 0 to 7% by mass, and more preferably from 0.3 to 5.0% by mass based on the overall mass of the second agent.
  • the content of the anionic polymer in the second agent is equal to or larger than the lower limit value, there tends to be no dropping of the oxidative hair dye during the application thereof and during the leaving time.
  • the content of the anionic polymer in the second agent is equal to or smaller than the upper limit value, application of the oxidative hair dye becomes easy for the overall hair and there tends to be no uneven dyeing.
  • the second agent has pH of preferably 2 to 5, and more preferably 2 to 4 at 25°C.
  • the hair dyeing property of the oxidative hair dye, which is used by mixing the first agent and the second agent is excellent.
  • the mass ratio of the first agent and the second agent is not particularly limited.
  • the mass ratio of the first agent and the second agent in the oxidative hair dye of the present invention (the first agent:the second agent) is preferably from 1:10 to 10:1, more preferably from 1:5 to 5:1, further more preferably from 1:4 to 3:1, and particularly more preferably from 1:3 to 2:1, from the viewpoint of the hair dyeing property.
  • the first agent and the second agent are each in a liquid form or a gel form.
  • the first agent and the second agent are each in a liquid form or a gel form, any uneven mixing can be suppressed when these agents are mixed with each other.
  • the oxidative hair dye of the present invention which is used by mixing the first agent and the second agent, is in a gel form or an emulsion form. Because the oxidative hair dye of the present invention has a proper viscosity, there tends to be no dropping thereof when the oxidative hair dye is applied to the hair, and application thereof becomes easy for the overall hair. Preferably, the oxidative hair dye of the present invention can be applied to the hair to be spread over the overall hair, concurrently being foamed. Forming the oxidative hair dye on the hair, which is applied to the hair, can cause the oxidative hair dye to evenly be supplied to each hair.
  • the foaming is executed in a manner of shampooing and the oxidative hair dye can be caused to sufficiently cling to the hair.
  • the foamed oxidative hair dye tends to generate no dropping thereof during the leaving time.
  • the hair can be dyed with a small use amount of oxidative hair dye, and therefore, the hair can economically be dyed.
  • the oxidative hair dye of the present invention which is used by mixing the first agent and the second agent, has a viscosity of preferably 100 to 2000 mPa.s, more preferably 200 to 1000 mPa.s, and further more preferably 350 to 1000 mPa.s at 25°C.
  • a viscosity of the oxidative hair dye is equal to or higher than the lower limit value, there tends to be no dropping thereof during the application thereof and during the leaving time.
  • the viscosity of the oxidative hair dye is equal to or lower than the higher limit value, application of the oxidative hair dye to the hair becomes further easy and the oxidative hair dye can be evenly supplied to each hair.
  • the oxidative hair dye of the present invention which is used by mixing the first agent and the second agent, has pH of preferably 7 to 12, and more preferably 8 to 11 at 25°C. When the oxidative hair dye has pH in this range, the hair dyeing property is excellent.
  • the oxidative hair dye of the present invention may be applied to dry hair or hair after washed with water and towel-dried, and the hair applied therewith may be left as it is for a predetermined time period, or the oxidative hair dye may be foamed on the hair and the hair may be left for a predetermine time period. After the predetermined time period elapses, the oxidative hair dye is washed with water from the hair and the hair is dried.
  • the time period from the application of the oxidative hair dye to the hair to the foaming thereof is preferably equal to or shorter than 10 minutes, more preferably equal to or shorter than five minutes, and further more preferably equal to or shorter than three minutes from the viewpoint of prevention of any dropping thereof.
  • the leaving time, which was the time from the foaming of the oxidative hair dye to the dyeing of the hair is preferably five minutes or longer and more preferably 10 minutes or longer, and the time is preferably 60 minutes or shorter and more preferably 40 minutes or shorter, from the viewpoint of the hair dyeing effect. After the hair dyeing sufficiently progresses, the oxidative hair dye is removed from the hair by washing.
  • oxidative hair dyes were each prepared, wherein each of oxidative hair dyes comprises the first agent and the second agent having the composition shown in Table 1.
  • the viscosity was measured for each of the oxidative hair dyes by means of the following method.
  • the first agent and the second agent were weighed to be 50 g in total at mixing ratio of 1:1 in a cylinder-shaped glass sample tube having the size of a diameter of 35 mm ⁇ a height of 78 mm, the lid of the tube was closed, the first agent and the second agent were mixed with each other to be a sufficiently mixed, and the obtained mixture was used.
  • the mixture was dipped in a constant temperature bath at 25°C for 30 minutes and the mixture was thereafter taken out of the constant temperature bath.
  • the viscosity of the mixture at 25°C was measured by means of a B-type viscosity meter (TVB-10M manufactured by Toki Sangyo Co., Ltd.) using a No. 3 rotor for one minute at 30 rpm and, when the viscosity was equal to or lower than 400 mPa.s, the viscosity was measured using a No. 2 rotor for one minute at 30 rpm. The result was presented in a value. The measurement was executed for three times and the average value of the obtained values was employed.
  • a B-type viscosity meter (TVB-10M manufactured by Toki Sangyo Co., Ltd.) using a No. 3 rotor for one minute at 30 rpm and, when the viscosity was equal to or lower than 400 mPa.s, the viscosity was measured using a No. 2 rotor for one minute at 30 rpm.
  • the result was presented in a value. The measurement was executed for three times and the
  • the following evaluation sessions were executed for each of the oxidative hair dyes prepared in the Examples and Comparative Examples.
  • the evaluation sessions were executed by five professional panelists and the evaluation was determined according to the following determination criteria. When the evaluation of the five professional panelists was split into two, the evaluation supported by the majority was employed and, when the evaluation was split into three, the test and the evaluation were again executed. Table 1 shows the results.
  • oxidative hair dye was used for the evaluation as that obtained by mixing 10 g of a first agent and 10 g of a second agent to be evenly mixed with each other. The evaluation was executed using a human head. The hair was firstly washed with a shampoo and the moisture of the hair was sufficiently swabbed using a towel. Then, the oxidative hair dye obtained in each of the Examples or Comparative Examples was applied to the hair. The five professional panelists determined dropping evaluation of the oxidative hair dye during the application thereof according to the following determination criteria. ⁇ Determination Criteria for Dropping during Application> A: There was no dropping at all. B: Liquid pools were generated but there was no dropping. C: There was a very small amount of dropping. D: There was dropping to obstruct the application.
  • Comparative Examples 1 to 7 wherein first agents each did not comprise any one of the anionic surfactant, the ampholytic surfactant and the alkyl glucoside-type nonionic surfactant, dissatisfactory results were obtained for the organoleptic evaluation sessions and the object of the present invention could not be achieved.
  • first agents each did not comprise any one of the anionic surfactant, the ampholytic surfactant and the alkyl glucoside-type nonionic surfactant
  • dissatisfactory results were obtained for the organoleptic evaluation sessions and the object of the present invention could not be achieved.
  • Example 1 (417 mPa.s)
  • Example 3 (609 mPa.s)
  • Example 8 (388 mPa.s)
  • Example 13 510 mPa.s
  • Comparative Examples 1, 3, and 7 the viscosities thereof were lower than 100 mPa.s and there was dropping and the application was obstructed.

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Abstract

La présente invention concerne un colorant capillaire oxydant utilisé en mélangeant un premier agent comprenant un agent alcalin et un second agent comprenant un agent d'oxydation. Ledit premier agent comporte 1 à 20 % en masse d'un colorant d'oxydation sur la base d'une masse totale du premier agent. En outre, ledit premier agent comprend au moins un tensioactif anionique, au moins un agent tensioactif ampholytique, et au moins un tensioactif non ionique de type glucoside d'alkyle, et le colorant capillaire par oxydation est sous forme de gel ou d'émulsion.
EP15775007.6A 2014-11-05 2015-09-10 Coloration capillaire oxydante Withdrawn EP3215114A1 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP2014225326A JP6636243B2 (ja) 2014-11-05 2014-11-05 酸化染毛剤
PCT/JP2015/004616 WO2016072040A1 (fr) 2014-11-05 2015-09-10 Coloration capillaire oxydante

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EP3215114A1 true EP3215114A1 (fr) 2017-09-13

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EP15775007.6A Withdrawn EP3215114A1 (fr) 2014-11-05 2015-09-10 Coloration capillaire oxydante

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EP (1) EP3215114A1 (fr)
JP (1) JP6636243B2 (fr)
WO (1) WO2016072040A1 (fr)

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JP7692592B2 (ja) * 2021-02-19 2025-06-16 株式会社アリミノ 酸性染毛料組成物

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DE10132915A1 (de) * 2001-07-06 2003-01-30 Wella Ag Oxidationshaarfärbemittel
DE102009027485A1 (de) * 2009-07-06 2011-01-13 Henkel Ag & Co. Kgaa Schaumförmige Färbemittel
EP2277499A1 (fr) * 2009-07-22 2011-01-26 KPSS-Kao Professional Salon Services GmbH Procédé de nivellement de couleur de cheveux
JP2011088867A (ja) * 2009-10-26 2011-05-06 Daicel Chemical Industries Ltd 二剤式染毛剤
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