DK160227B - Means for simultaneous dyeing by way of toning, washing and conditioning of human hair - Google Patents
Means for simultaneous dyeing by way of toning, washing and conditioning of human hair Download PDFInfo
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- DK160227B DK160227B DK335381A DK335381A DK160227B DK 160227 B DK160227 B DK 160227B DK 335381 A DK335381 A DK 335381A DK 335381 A DK335381 A DK 335381A DK 160227 B DK160227 B DK 160227B
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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
- A61K8/30—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
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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
- A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
- A61K8/73—Polysaccharides
- A61K8/731—Cellulose; Quaternized cellulose derivatives
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- 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
- A61Q5/02—Preparations for cleaning the hair
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- 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
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- 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
- A61Q5/12—Preparations containing hair conditioners
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- 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
- A61K2800/54—Polymers characterized by specific structures/properties
- A61K2800/542—Polymers characterized by specific structures/properties characterized by the charge
- A61K2800/5426—Polymers characterized by specific structures/properties characterized by the charge cationic
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- 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
Abstract
Description
DK 160227 BDK 160227 B
Opfindelsen angår et middel på basis af oxidationsfarvestoffer til farvning henholdsvis toning, vask og konditionering af menneskehår omfattende et oxidationsfarvemiddel, som indeholder sædvanlige oxidationsfarvestoffer og kosmetiske hjælpemid-5 ler.The invention relates to an oxidation dye-based agent for dyeing, toning, washing and conditioning human hair, respectively, comprising an oxidizing dye containing usual oxidation dyes and cosmetic aids.
Det er kendt, at det ved hjælp af oxidat ionsfarvestoffer farvede henholdsvis tonede hår uden en speciel efterbehandling ikke er glansfuldt, er hårdt at føle på og kun vanskeligt kan 10 redes igennem. For at afhjælpe disse mangler er det allerede blevet anbefalet i en efterfølgende særskilt behandling med skylning på basis af kationiske produkter, at bibringe det ved hjælp af hårfarvemidler på basis af oxidationsfarvestoffer farvede henholdsvis tonede og særskilt vaskede hår, den tid-15 ligere eksisterende glans, fyldighed og evne til let at kunne redes igennem. I den tyske patentansøgning P 26 51 749.7 blev det allerede foreslået at reducere disse nødvendige 3-trin af hårbehandl i ng, farvn i ng/ton ing, vask og kond i tioner i ng t i 1 2-trin. Til dette formål blev håret først behandlet med et 20 specielt hårfarvemiddel indeholdende et oxidationsfarvemiddel, en kation i sk polymer og et an i on i sk tensid af sul fattypen og derpå med en speciel shampoo, som indeholder mindst et anio-nisk tensid og fortrinsvis yderligere en kationisk polymer.It is known that, with the aid of oxidation dyes, colored and tinted hairs without a special finishing treatment are not glossy, hard to feel and only difficult to penetrate. To remedy these deficiencies, it has already been recommended in a subsequent separate treatment with rinsing based on cationic products to impart, by means of hair dyes based on oxidation dyes, tinted and separately washed hair, the previously existing gloss, fullness and ability to be easily traced. In German patent application P 26 51 749.7, it was already proposed to reduce these necessary 3 steps of hair treatment in ng, dye in ng / ton ing, washing and cond inions in ng t in 1 2 steps. For this purpose, the hair was first treated with a special hair dye containing an oxidizing dye, a cation in so-called polymer and an in-on so-called surfactant of the sulphate type and then with a special shampoo containing at least one anionic surfactant and preferably further a cationic polymer.
25 Det har nu vist sig, at f arvn ingen henholdsvig toningen og konditioneringen af menneskehår kan gennemføres i én arbejdsgang med et middel, som består af en blanding af et oxidationsfarvemiddel, som indeholder sædvanlige oxidationsfarvestoffer og kosmetiske hjælpemidler, og er ejendommelig ved det i 30 krav l's kendetegnende del anførte.It has now been found that no corresponding toning and conditioning of human hair can be accomplished in one operation with an agent consisting of a mixture of an oxidizing dye containing the usual oxidation dyes and cosmetic aids, and is peculiar to it. Claim 1 of the Characteristic Part.
Ved de ifølge opfindelsen anvendte sædvanlige oxidationsfarvestoffer drejer det sig om aromatiske forbindelser, som ved hjælp af oxidationsmidler kan kondenseres til de egentligt 35 farvende forbindelser. Herved skelner man mellem fremkalder stofferne såsom, f.eks. p-phenylendiamin, p-toluylendiamin, o-phenylendiamin, o-toluylendiamin, p-aminophenol, p-aminodi-The usual oxidation dyes used according to the invention are aromatic compounds which can be condensed by means of oxidants to the actual coloring compounds. Hereby one distinguishes between developing substances such as, e.g. p-phenylenediamine, p-toluylenediamine, o-phenylenediamine, o-toluylenediamine, p-aminophenol, p-aminodiamine
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2 ! i phenylamin, o-aminophenol, 2,3,5,6-tetraaminopyrimidin, 4-a- minopyrazolonderivater, heterocykli ske hydrazoner og koblingskomponenterne, såsom f.eks. resorcin, 2-methyl resorcin, α-naphthol, 2,7-dihydroxynaphthalin, pyrocatecol, hydroquinon, 5 1,5-dihydroxynaphthalin, m-phenylendiamin og derivater heraf, m-aminopheny1, m-toluylendiamin, 2,4-diaminoanisoT, 2,6-di-aminopyri din. i2! in phenylamine, o-aminophenol, 2,3,5,6-tetraaminopyrimidine, 4-aminopyrazolone derivatives, heterocyclic hydrazones and the coupling components such as e.g. resorcin, 2-methyl resorcin, α-naphthol, 2,7-dihydroxynaphthaline, pyrocatecol, hydroquinone, 1,5-dihydroxynaphthalin, m-phenylenediamine and derivatives thereof, m-aminophenyl, m-toluylenediamine, 2,4-diaminoanisoT , 6-di-aminopyri. in
De farvende præparaters koncentration af kobler-fremkalder-10 kombination udgør 0,02 - 5 vægt%. !The concentration of the coupler-developer-10 combination of the staining compositions is 0.02 to 5% by weight. !
De sædvanlige kosmetiske hjælpestoffer, der skal anvendes i forbindelse med opfindelsen, tjener i første række til at bringe midlet på en velegnet form, som f.eks. creme, emulsion, 15 gel eller eventuelt en simpel opløsning. Som sådanne yderligere bestanddele skal f.eks. nævnes befugtnings- eller emulgeringsmidler af den anioniske eller ikke-ionogene type, såsom al kyl benzensulfater, fedtsyrealkanolamider, additionsprodukter af ethylenoxid og fedtalkoholer, fortykkelsesmidler såsom 20 methylcellulose, stivelse, højere fedtalkoholer, paraffinolie, fedtsyrer. Disse tilsætningsstoffer anvendes i det til disse formål sædvanlige mængder, således f.eks. befugtnings- og emulgeringsmidler i koncentrationer fra 0,5 - 30 vægt% og fortykkelsesmidler i koncentrationer fra 0,1 - 25 vægt%, i hvert 25 tilfælde beregnet på præparatets samlede vægt. Til de kosmetiske hjælpemidler hører desuden parfumeolier og hårplejemidler, såsom pantothensyre og cholesterol.The usual cosmetic auxiliaries to be used in connection with the invention primarily serve to bring the agent into a suitable form, such as e.g. cream, emulsion, 15 gel or optionally a simple solution. As such additional components, e.g. wetting or emulsifying agents of the anionic or nonionic type such as alkyl benzene sulphates, fatty acid alkanolamides, ethylene oxide and fatty alcohol additives, thickeners such as methyl cellulose, starch, higher fatty alcohols, paraffin oil, fatty acids are mentioned. These additives are used in the usual amounts for these purposes, e.g. wetting and emulsifying agents at concentrations from 0.5 to 30% by weight and thickeners at concentrations from 0.1 to 25% by weight, in each 25 cases based on the total weight of the composition. The cosmetic aids also include perfume oils and hair care products such as pantothenic acid and cholesterol.
Egnede anioniske tensider af sulfattypen er svovlsyremonoe-30 esterne af primære alkoholer (f.eks. af kokosfedtalkoholer, talgfedtalkoholer eller oleylal kohol) og sådanne sekundære alkoholer. Yderligere egner sig sulfaterede fedtsyrealkanolamider, fedtsyremonoglycerider eller reaktionsprodukter af 1 - 4 mol ethylenoxid med primære eller sekundære fedtalkoholer 35 eller alkylphenoler.Suitable sulphate-type anionic surfactants are the sulfuric acid monoesters of primary alcohols (e.g., of coconut fatty alcohols, sebum fatty alcohols or oleylal alcohols) and such secondary alcohols. Furthermore, sulfated fatty acid alkanolamides, fatty acid monoglycerides or reaction products of 1-4 moles of ethylene oxide with primary or secondary fatty alcohols or alkyl phenols are suitable.
Blandt de anioniske tensider er fedtalkoholethersulfaterne af særlig betydning, specielt sådanne med den almene formel 3Among the anionic surfactants, the fatty alcohol ether sulfates are of particular importance, especially those of the general formula 3
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R-(CH2CH20)nCH2CH20S03Me, hvori R betegner en alkylgruppe med 10-16 carbonatomer, n er et tal fra 1 til 3, og Me er en saltdannende base.R - (CH 2 CH 2 O) nCH 2 CH 2 SO 3 Me, wherein R represents an alkyl group of 10-16 carbon atoms, n is a number from 1 to 3, and Me is a salt-forming base.
5 De anioniske tensider kan foreligge i form af deres natrium-, kalium- og ammoniumsalte samt som opløselige salte af organiske baser, såsom mono-, di- eller triethanolamin. De indgår i midlerne ifølge opfindelsen i en mængde på 1-25 vægt% beregnet på midlets samlede vægt.The anionic surfactants may be in the form of their sodium, potassium and ammonium salts as well as soluble salts of organic bases such as mono-, di- or triethanolamine. They are included in the compositions of the invention in an amount of 1-25% by weight based on the total weight of the composition.
1010
De amfotere eller zwitterioniske tensider, der skal anvendes i midlet ifølge opfindelsen, indeholder i molekylet såvel sure grupper, såsom f.eks. carboxyl-, sulfo-, svovl syrehalvestere-, phosphon- eller phosphorsyredelestergrupper, som basisk grup-15 pe, såsom f.eks. amino-, imino- eller ammoniumgrupper. Zwitterioniske forbindelser med en 4 gange substitueret, det vil sige kvaternær ammoniumgruppe, betegnes som betainer, når de i molekylet også har en kovalent bundet syregruppe, og den positive og negative ladning er udlignet intramolekylært. I videre 20 betydning omfatter klassen af betainer også de tilsvarende substituerede kvaternære phosphonium- og tertiære sulfonium-forbindelser. De overfladeaktive betainer har ved nitrogenatomet i almindelighed en højmolekylær alifatisk hydrocarbongrup-pe med hydrofob karakter og to lavere alkylgrupper med 1-3 25 carbonatomer, som kan være substitueret med én eller to hydro-xygrupper eller kan være forbundet med hinanden direkte eller via et heteroatom. Den vandopløseliggørende carboxylat-, sul-fonat- eller sulfatgruppe er forbundet med aminonitrogenet via den fjerde substituent, som for det meste består af en kort-30 kædet alifatisk gruppe, som eventuelt har en dobbeltbinding eller en hydroxylgruppe. Som tensider egner sig også sådanne sulfonatbetainer, ved hvilke den anioniske, vandopløseliggørende gruppe er bundet direkte til den langkædede hydrofobe hydrocarbongruppe, der er ansvarlig for kapilarvirkningen.The amphoteric or zwitterionic surfactants to be used in the composition of the invention contain in the molecule both acidic groups such as e.g. carboxylic, sulfo, sulfuric acid half-esters, phosphonic or phosphoric acid ester groups such as basic groups, such as e.g. amino, imino or ammonium groups. Zwitterionic compounds having a 4-fold substituted, i.e., quaternary ammonium group, are referred to as betaines when in the molecule they also have a covalently bonded acid group and the positive and negative charges are offset intramolecularly. In a further sense, the class of betaine also includes the corresponding substituted quaternary phosphonium and tertiary sulfonium compounds. The surfactant betaines generally have at the nitrogen atom a high molecular weight aliphatic hydrocarbon group of hydrophobic character and two lower alkyl groups of 1-3 carbon atoms which may be substituted by one or two hydroxy groups or may be linked directly or via a heteroatom . The water-solubilizing carboxylate, sulfonate or sulfate group is connected to the amino nitrogen via the fourth substituent, which is mostly a short-chain aliphatic group optionally having a double bond or a hydroxyl group. Also suitable as surfactants are such sulfonate betaines in which the anionic water-solubilizing group is directly linked to the long-chain hydrophobic hydrocarbon group responsible for the capillary action.
35 Sådanne sulfobetainer kan f.eks. fås af de af Cg-C2o-a-°lefi-ner med SO3 fremstillelige sultoner og en tertiær amin med tre kortkædede alifatiske grupper. Typiske eksempler på sådan- 4Such sulfobetaines may e.g. are obtained from the Cg-C20-a-° lefins with SO3-produced sultones and a tertiary amine with three short-chain aliphatic groups. Typical examples of such 4
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ne overfladeaktive betainer er f.eks. forbindelserne 3-(N-he-xadecyl-N,N-di methyl-ammonium)-propansul fonat, 3-(N-tal gal kyl-N,N-di methyl ammon i um)-2-hydroxypropansu1 fonat, 3-(N-hexade- cyl-N,N-bi s-(2-hydroxyethy1)-ammoni um)-2-hydroxypropy1-sulfat, i 5 3-{N-kokosalkyl-N,N-bis(2,3-dihydroxypropyl)-ammon ium)propan-sulfonat, N-tetradecyl-N,N-dimethylammoniumacetat, N-hexade-cyl-N,N-bis-(2,3-di hydroxypropy1)-ammoniumacetat.ne surfactant betaine is e.g. compounds 3- (N-hexadecyl-N, N-di-methyl-ammonium) -propanesulfonate, 3- (N-number gal-N, N-di-methyl-ammonium) -2-hydroxypropane sulfonate, 3- (N-hexadecyl-N, N-bi s- (2-hydroxyethyl) ammonium) -2-hydroxypropyl sulfate, in 3- {N-cocoalkyl-N, N-bis (2,3-dihydroxypropyl) ) -ammonium propane sulfonate, N-tetradecyl-N, N-dimethylammonium acetate, N-hexadecyl-N, N-bis (2,3-di hydroxypropyl) -ammonium acetate.
Disse overfladeaktive betainer kan f.eks. fremstilles ved at 10 man omsætter den tertiære amin med den hydrofobe, langkædede alifatiske hydrocarbongruppe og de to lavere alkyl- eller hy-droxyalkylgrupper med kvaterniseringsmidler, såsom f.eks.These surfactant betainees can e.g. is prepared by reacting the tertiary amine with the hydrophobic, long chain aliphatic hydrocarbon group and the two lower alkyl or hydroxyalkyl groups with quaternizing agents such as e.g.
3-chlor-2-hydroxypropannatri umsulfonat, 3-chlor-2-hydroxypro-pylnatriumsulfat, natriumchloracetat eller propansul ton, bu-15 tansulton eller carbylsulfat. De amfotere tensider indgår i midlerne ifølge opfindelsen i en mængde på 1-5 vægt%, beregnet på midlets samlede vægt. Forholdet af anioniske tensider til amfotere tensider kan i midlerne ifølge opfindelsen ligge i intervallet fra 5:1 til 1:1.3-chloro-2-hydroxypropane sodium sulfonate, 3-chloro-2-hydroxypropyl sodium sulfate, sodium chloroacetate or propanesulton, butsultultone or carbyl sulfate. The amphoteric surfactants are included in the compositions of the invention in an amount of 1-5% by weight, based on the total weight of the composition. The ratio of anionic surfactants to amphoteric surfactants may in the compositions of the invention range from 5: 1 to 1: 1.
2020
Ved kationiske polymerer, som anvendes i midlerne ifølge opfindelsen drejer det sig om produkter af forskellig opbygning, som er fælles om nærværelsen af en række kvaternære nitrogenatomer. De kvaternære celluloseetherderivater, som er beskre-25 vet i fransk patentskrift nr. 1.492.597, har herved vist sig at være en særligt egnet produktgruppe. Forbindelserne kan fremstilles ifølge den der beskrevne fremgangsmåde ved for-ethring og kvaternisering, idet den nødvendige omsætning kan gennemføres i vilkårlig rækkefølge eller også samtidigt. Det 30 drejer sig f.eks. om forbindelser, som dannes ved omsætning af hydroxyethylcellulose med reaktionsproduktet af 0,7 mol epi-chlorhydrin og 0,7 mol trimethylamin pr. substitueret anhydro-glucoseenhed. Som handelsprodukter, der falder ind under denne gruppe af kvaternære celluloseetherderivater, skal nævnes 35 IR 400, IR 30 M og IR 125 (handelsnavne for af Union Carbide® leverede produkter). Blandt de kvaternære cel!ulosederivater har produktet IR 400 særlig betydning, idet det giver de bed- 5In the case of cationic polymers used in the compositions of the invention, these are products of different structure which are common to the presence of a number of quaternary nitrogen atoms. The quaternary cellulose ether derivatives disclosed in French Patent Specification No. 1,492,597 have hereby been found to be a particularly suitable product group. The compounds can be prepared according to the process described by etherification and quaternization, the necessary reaction being carried out in any order or at the same time. It is about e.g. on compounds formed by reaction of hydroxyethyl cellulose with the reaction product of 0.7 mole of epichlorohydrin and 0.7 mole of trimethylamine per liter. substituted anhydro glucose unit. As trading products falling under this group of quaternary cellulose ether derivatives, mention should be made of 35 IR 400, IR 30 M and IR 125 (trade names for Union Carbide® products supplied). Among the quaternary cellulose derivatives, the product IR 400 is of particular importance as it provides the bed
DK 160227 BDK 160227 B
ste egenskaber med henblik på let gennemredning af håret, glans og fyldighed af det behandlede hår.properties for easy penetration of the hair, shine and fullness of the treated hair.
Yderligere egnede kationiske polymerer til anvendelse i mid-5 lerne ifølge opfindelsen er polymerisater med ringstruktur af den almene formelFurther suitable cationic polymers for use in the agents of the invention are polymerizers of ring structure of the general formula
A BA B
ν' · / \ ch2 fa I ^R*ν '· / \ ch2 fa I ^ R *
R C CR C C
---*C / ^CH9----- * C /
15 ^ CT2 J15 ^ CT2 J
således som disse er beskrevet nærmere i det amerikanske patentskrift nr. 3.288.770. Desuden kan principielt anvendes 20 alle andre kendte kvaterniserede polymerisater, således som disse f.eks. er beskrevet nærmere i tysk patentansøgning nr. P 25 21 960, tysk patentansøgning nr. P 26 29 922 og amerikansk patentskrift nr. 4.175.572.as these are described in greater detail in U.S. Patent No. 3,288,770. In addition, in principle, all other known quaternized polymerisates such as these, e.g. are described in greater detail in German Patent Application No. P 25 21 960, German Patent Application No. P 26 29 922 and US Patent No. 4,175,572.
25 De kationiske polymerer anvendes i midlerne ifølge opfindelsen i en mængde på 0,5 - 4 vægt% beregnet på midlets samlede vægt.The cationic polymers are used in the compositions of the invention in an amount of 0.5 to 4% by weight based on the total weight of the agent.
Fremstillingen af midlet ifølge opfindelsen sker på sædvanlig måde ved indarbejdning af farvestofkomponenterne i en bærer i 30 creme-, emulsion- eller gelform, som består af en blanding af aniontensid, amfotert tensid, kationisk polymer og yderligere nødvendige befugtnings-, emulgerings-, fortykkelsesmidler, hårplejemidler, duftstoffer og vand. Såfremt opnåelsen af en ønsket farvetone kræver, at der også anvendes direkte farven-35 de farvestoffer, indarbejdes disse ligeledes med oxidationsfarvestofkomponenterne i bæreren.The preparation of the agent according to the invention is carried out in the usual manner by incorporating the dye components into a carrier in cream, emulsion or gel form consisting of a mixture of anionic surfactant, amphoteric surfactant, cationic polymer and further necessary wetting, emulsifying, thickening agents. hair care products, fragrances and water. If the attainment of a desired tint requires that directly dyed dyes are also used, these are also incorporated with the oxidation dye components in the carrier.
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66
SS
Den oxidative kobling, det vil sige fremkaldelsen af farven, foretages hensigtsmæssigt ved hjælp af kemiske oxidationsmidler. Som sådanne kommer specielt hydrogenperoxid og dets additionsprodukter med urinstof, melamin og natriumborat samt 5 blandinger af sådanne hydrogenperoxid-additionsforbindelser med kaliumperoxiddisulfat i betragtning.The oxidative coupling, i.e. the development of the color, is conveniently made by chemical oxidizing agents. As such, especially hydrogen peroxide and its addition products with urea, melamine and sodium borate as well as 5 mixtures of such hydrogen peroxide addition compounds with potassium peroxide disulfate are considered.
Til behandlingen af håret til samtidig farvn i ng/toning, vask og konditionering blandes det af bærerbasis og farvestofkom-10 ponenter bestående præparat umiddelbart før anvendelsen med ét af de nævnte oxidationsmidler. Anvendelsen af midlet ifølge opfindelsen kan, uafhængigt af om det drejer sig om en opløsning, en emulsion, en creme eller en gel, ske i svagt sur, neutral eller specielt alkalisk miljø ved en pH-værdi fra 8 15 til 10. Anvendelsestemperaturen ligger derved i området fra 15°c til 40°C. Efter en indvirkningstid på 10 til 45 minutter frembringes der med vand et skum i håret, og dette skylles derpå omhyggeligt. Håret er efter denne 1-trins behandling blevet farvet henholdsvis tonet i den ønskede farvetone, og 20 det er let at gennemrede håret i fugtig tilstand, og efter tørring er håret glansfuldt og fyldigt og behageligt at føle på. Fordelen ved anvendelsen af midlet ifølge opfindelsen består i, at man i ét enkelt behandlingstrin opnår at håret farves henholdsvis tones, vaskes, gøres let at rede igennem og 25 kan behandles i den sædvanlige glansfulde, bløde, fyldige tilstand.For the treatment of the hair for simultaneous staining in ng / toning, washing and conditioning, the composition of carrier and dye components is blended immediately prior to use with one of said oxidizing agents. The use of the composition according to the invention, regardless of whether it is a solution, an emulsion, a cream or a gel, can be effected in a slightly acidic, neutral or especially alkaline environment at a pH of from 8 to 10. The application temperature is thereby in the range of 15 ° C to 40 ° C. After an action of 10 to 45 minutes, a foam is produced with water in the hair, which is then rinsed carefully. After this one-step treatment, the hair has been dyed or tinted in the desired tint, respectively, and it is easy to permeate the hair in a moist state, and after drying the hair is glossy and full and comfortable to feel. The advantage of using the agent according to the invention consists in the fact that in a single treatment step, the hair is dyed or tinted, washed, made easy to clean and can be treated in the usual glossy, soft, full condition.
De efterfølgende eksempler skal belyse den foreliggende opfindelse nærmere.The following examples will illustrate the present invention in more detail.
30 3530 35
. DK 160227 B. DK 160227 B
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Eksempler 1. Hårfarvemiddel: Middelblond: Vasker og konditionerer samtidigt 5Examples 1. Hair dye: Medium blonde: Wash and condition simultaneously 5
Fedtalkohol Ci2~18 10,5 vægtdeleFatty alcohol Ci2 ~ 18 10.5 parts by weight
Natriumlaurylethersulfat 6,0 "Sodium lauryl ether sulfate 6.0 "
Kokosalkyl-dimethylammoniumbetain 3,0 "Coconutalkyl dimethylammonium betaine 3.0 "
Polymer IR 400 (Union Carbide®) 1,0 " 10 a-Naphthol 0,04 " 1,3-bi s-(2,4-diaminophenoxy)-propan 0,01 "Polymer IR 400 (Union Carbide®) 1.0 "10 α-Naphthol 0.04" 1,3-bi s- (2,4-diaminophenoxy) propane 0.01 "
Resorcin 0,15 " p-Toluy1endiaminsu1fat 0,21 "Resorcin 0.15 "p-Toluylenediamine sulfate 0.21"
Trilon® BS (ethylendiamintetraeddikesyre) 0,20 " 15 Natriumsulfit 1,00 "Trilon® BS (Ethylenediaminetetraacetic Acid) 0.20 "Sodium Sulfite 1.00"
Ammoniak 25%'ig 6,00 "Ammonia 25% 6.00 "
Vand 72,89 __ 20 vægtdele af den ovennævnte blanding blev umiddelbart før 20 anvendelsen blandet med 20 vægtdele 6%'ig hydrogenperoxid-opløsning. Blandingen blev anbragt på lyseblondt hår. Efter en indvirkningstid på 30 minutter blev der fremkaldt skum med en ringe mængde vand og derpå skyllet omhyggeligt. Efter behandlingen var hårets farve middelblond, og det kunne let gennem-25 redes i fugtig tilstand. Efter tørringen havde håret en silkeagtig glans og et tiltalende blødt og fyldigt greb.Water 72.89 20 20 parts by weight of the above mixture was mixed immediately before use with 20 parts by weight of 6% hydrogen peroxide solution. The mixture was applied to light blonde hair. After a 30 minute action, foam with a small amount of water was developed and then rinsed carefully. After treatment, the color of the hair was medium blonde and could easily be moisturized. After drying, the hair had a silky shine and an appealing soft and full grip.
30 3530 35
DK 160227 BDK 160227 B
8 2. Hårtoningsmiddel; Gyldent kobberfarvet; Vasker og konditionerer samtidig8 2. Hair toning agent; Golden copper color; Wash and condition at the same time
Fedtalkohol £\2-\s 10,5 vægtdele 5 Natriumkokosalkylethersulfat 5,0 " N-tetradecyl-N,N-dimethylammoniumacetat 3,0 "10.5 parts by weight of sodium cocosalkyl ether sulfate 5.0 "N-tetradecyl-N, N-dimethylammonium acetate 3.0"
Polymer IR 400 1,0 " 2,4,5,6-tetraaminopyrimidinsulfatmonohydrat 0,30 " 2-methylresorcin 0,075 " 10 2,7-dihydroxynaphthalin 0,075 " m-aminophenol 0,01 "Polymer IR 400 1.0 "2,4,5,6-tetraaminopyrimidine sulfate monohydrate 0.30" 2-methylresorcin 0.075 "2,7-dihydroxynaphthaline 0.075" m-aminophenol 0.01 "
Resorcin 0,05 " p-toluylendiaminsulfat 0,10 *' p-aminophenolhydrochlorid 0,15 " 15 Tri Ion® BS 0,20Resorcin 0.05 "p-toluylenediamine sulfate 0.10 * 'p-aminophenol hydrochloride 0.15" Tri Ion® BS 0.20
Natriumsulfit 1,00 "1.00 "sodium sulfite
Ammoniak 25%*ig 6,00 "Ammonia 25% * 6.00 "
Vand 72,54 *'_ 20 20 vægtdele af ovennævnte blanding blev umiddelbart før anven delsen blandet med 20 vægtdele 6%'ig hydrogenperoxidopløsning. Blandingen blev anbragt på lysebrunt hår. Efter 20 minutters indvirkningstid blev blandingen bragt til at skumme i håret med en ringe mængde vand, hvorefter håret blev skyllet grun-25 digt. Efter behandlingen var håret tonet gyldent kobberfarvet, og det var let at rede igennem i fugtig tilstand. Efter tørringen havde håret en silkeagtig glans og et blødt fyldigt greb.Water 72.54 * 20 parts by weight of the above mixture were mixed immediately before use with 20 parts by weight of 6% hydrogen peroxide solution. The mixture was applied to light brown hair. After 20 minutes of action, the mixture was made to foam in the hair with a small amount of water, after which the hair was rinsed thoroughly. After treatment, the hair was tinted golden copper and it was easy to brush through in a moist condition. After drying, the hair had a silky shine and a soft full grip.
30 3530 35
Claims (6)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE19803031535 DE3031535A1 (en) | 1980-08-21 | 1980-08-21 | MEDIUM FOR SIMULTANEOUS COLORING OR TOENING, WASHING AND CONDITIONING HUMAN HAIR |
DE3031535 | 1980-08-21 |
Publications (3)
Publication Number | Publication Date |
---|---|
DK335381A DK335381A (en) | 1982-02-22 |
DK160227B true DK160227B (en) | 1991-02-18 |
DK160227C DK160227C (en) | 1991-07-22 |
Family
ID=6110100
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
DK335381A DK160227C (en) | 1980-08-21 | 1981-07-27 | Means for simultaneous dyeing by way of toning, washing and conditioning of human hair |
Country Status (7)
Country | Link |
---|---|
EP (1) | EP0046543B1 (en) |
JP (1) | JPS5770812A (en) |
AT (1) | ATE13011T1 (en) |
DE (2) | DE3031535A1 (en) |
DK (1) | DK160227C (en) |
FI (1) | FI76926C (en) |
NO (1) | NO155086C (en) |
Families Citing this family (15)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE4120361C3 (en) * | 1991-06-20 | 1998-05-20 | Goldwell Gmbh | Hair dye |
US5393305A (en) * | 1993-08-26 | 1995-02-28 | Bristol-Myers Squibb Company | Two-part aqueous composition for coloring hair, which forms a gel on mixing of the two parts |
JP3816122B2 (en) * | 1993-12-27 | 2006-08-30 | 株式会社資生堂 | Mixed hair dye composition and method for use |
DE4421032A1 (en) * | 1994-06-16 | 1995-12-21 | Henkel Kgaa | Oxidation hair dye in gel form |
FR2721207A1 (en) * | 1994-06-21 | 1995-12-22 | Oreal | Oxidation tincture of keratinous fibers based on 2- (B-hydroxyethyl) paraphenylenediamine of 2-methylresorcin and resorcinol, and use. |
PL195678B1 (en) | 1998-03-06 | 2007-10-31 | Oreal | Method of and cationic amphophilic polymer containing compositions for oxidisingly dyeing creatine fibre |
JP2003530334A (en) * | 2000-04-07 | 2003-10-14 | ザ、プロクター、エンド、ギャンブル、カンパニー | Hair coloring and conditioning compositions |
JP4312980B2 (en) | 2001-12-26 | 2009-08-12 | 花王株式会社 | Hair dye composition |
US6758867B2 (en) * | 2001-12-28 | 2004-07-06 | Unilever Home & Personal Care Usa, Division Of Conopco, Inc. | Gradual permanent coloring of hair using dye intermediates in a shampoo base |
US6726729B2 (en) | 2001-12-28 | 2004-04-27 | Unilever Home & Personal Care Usa, Division Of Conopco, Inc. | Gradual permanent coloring of hair using dye intermediates in a shampoo base |
US6709468B2 (en) | 2002-03-07 | 2004-03-23 | Unilever Home & Personal Care Usa | Gradual permanent coloring of hair using dye intermediates in alkaline water which contains quaternary ammonium compounds |
US6736860B2 (en) | 2002-03-12 | 2004-05-18 | Unilever Home & Personal Care Usa Division Of Conopco, Inc. | Gradual permanent coloring of hair using dye intermediates dissolved in alkaline water with fatty alcohol |
DE102004046222A1 (en) * | 2004-09-22 | 2006-03-23 | Henkel Kgaa | Hair treating agent, useful for the treatment of keratin fibers and improvement of the combing bareness and/or handling of human hair, comprises a keratin-reducing substance |
DE102005014686A1 (en) * | 2005-03-29 | 2006-10-12 | Henkel Kgaa | Oxidation colorant with 1,5- and / or 2,7-dihydroxynaphthalene and at least one further coupler |
DE102018209894A1 (en) * | 2018-06-19 | 2019-12-19 | Henkel Ag & Co. Kgaa | Oxidative hair lightening or hair dye with improved application properties |
Family Cites Families (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB1394353A (en) * | 1972-06-29 | 1975-05-14 | Gillette Co | Hair treating composition |
CA1018893A (en) * | 1972-12-11 | 1977-10-11 | Roger C. Birkofer | Mild thickened shampoo compositions with conditioning properties |
CA1022075A (en) * | 1973-05-17 | 1977-12-06 | Earl L. Richardson | Shampoo formulations comprising a quaternary nitrogen containing cellulose polymer |
LU72592A1 (en) * | 1975-05-28 | 1977-02-10 | ||
DE2549293C2 (en) * | 1975-11-04 | 1985-05-30 | Henkel KGaA, 4000 Düsseldorf | Preparations for reducing the damage to hair during bleaching and dyeing |
NL7612554A (en) * | 1975-11-13 | 1977-05-17 | Oreal | METHOD OF DYING HAIR. |
FR2382233A1 (en) * | 1977-03-02 | 1978-09-29 | Oreal | NEW COSMETIC COMPOSITIONS FOR HAIR AND APPLICATION METHOD |
FR2402446A1 (en) * | 1977-09-07 | 1979-04-06 | Oreal | Hair dyeing compsn. contg. specified cationic polymer - fatty acid, alkali, benzyl alcohol and oxidn. dye |
FR2470596A1 (en) * | 1979-11-28 | 1981-06-12 | Oreal | COMPOSITION FOR THE TREATMENT OF KERATIN FIBERS BASED ON AMPHOTERIC POLYMERS AND CATIONIC POLYMERS |
-
1980
- 1980-08-21 DE DE19803031535 patent/DE3031535A1/en active Granted
-
1981
- 1981-07-27 DK DK335381A patent/DK160227C/en not_active IP Right Cessation
- 1981-07-27 NO NO812564A patent/NO155086C/en unknown
- 1981-07-27 FI FI812344A patent/FI76926C/en not_active IP Right Cessation
- 1981-08-13 DE DE8181106306T patent/DE3170286D1/en not_active Expired
- 1981-08-13 AT AT81106306T patent/ATE13011T1/en not_active IP Right Cessation
- 1981-08-13 EP EP81106306A patent/EP0046543B1/en not_active Expired
- 1981-08-20 JP JP56129477A patent/JPS5770812A/en active Granted
Also Published As
Publication number | Publication date |
---|---|
DK160227C (en) | 1991-07-22 |
EP0046543B1 (en) | 1985-05-02 |
DE3031535C2 (en) | 1987-10-15 |
ATE13011T1 (en) | 1985-05-15 |
FI76926C (en) | 1989-01-10 |
FI76926B (en) | 1988-09-30 |
NO812564L (en) | 1982-02-22 |
EP0046543A2 (en) | 1982-03-03 |
DE3031535A1 (en) | 1982-04-08 |
EP0046543A3 (en) | 1982-06-02 |
NO155086B (en) | 1986-11-03 |
JPS5770812A (en) | 1982-05-01 |
DK335381A (en) | 1982-02-22 |
DE3170286D1 (en) | 1985-06-05 |
NO155086C (en) | 1987-02-11 |
FI812344L (en) | 1982-02-22 |
JPH0422884B2 (en) | 1992-04-20 |
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Legal Events
Date | Code | Title | Description |
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PBP | Patent lapsed |