WO1991003229A1 - Preparations pour soins capillaires - Google Patents

Preparations pour soins capillaires Download PDF

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Publication number
WO1991003229A1
WO1991003229A1 PCT/EP1990/001444 EP9001444W WO9103229A1 WO 1991003229 A1 WO1991003229 A1 WO 1991003229A1 EP 9001444 W EP9001444 W EP 9001444W WO 9103229 A1 WO9103229 A1 WO 9103229A1
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WO
WIPO (PCT)
Prior art keywords
hair
preparations according
monomers
group
groups
Prior art date
Application number
PCT/EP1990/001444
Other languages
German (de)
English (en)
Inventor
Reinhard Müller
Klaus-Dieter Wisotzki
Karl Giede
Jutta Bernike
Horst Höffkes
Kurt Seidel
Iduna Matzik
Dieter Schrader
Adolf Klenk
Kurt Dahmen
Helmut Klimmek
Original Assignee
Henkel Kommanditgesellschaft Auf Aktien
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 Kommanditgesellschaft Auf Aktien filed Critical Henkel Kommanditgesellschaft Auf Aktien
Publication of WO1991003229A1 publication Critical patent/WO1991003229A1/fr

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Classifications

    • 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
    • A61K8/81—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
    • A61K8/8141—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides or nitriles thereof; Compositions of derivatives of such polymers
    • A61K8/8158—Homopolymers or copolymers of amides or imides, e.g. (meth) acrylamide; Compositions of derivatives of such polymers
    • 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

Definitions

  • the invention relates to preparations for hair treatment which contain zwitterionic polymers.
  • Polymeric compounds are frequently used as active ingredients that improve hair properties.
  • Cationic polymers such as, for example, the cellulose derivatives known from the American patents US 3,816,616 and US 3,472,840, can significantly improve wet combability, but only achieve unsatisfactory hair-setting and hair-stabilizing effects.
  • zwitterionic polymers which contain anionic groups, usually carboxyl groups, and quaternary ammonium groups in the molecule in hair treatment compositions.
  • DE-OS 21 50 557 describes the use of polymers of zwitterionic monomers in hair fixatives.
  • DE-OS 28 17 369 also disclosed the use of copolymers of dimethylaminoethyl methacrylate, acrylic acid and methyl methacrylate in hair fixatives and shampoos.
  • zwitterionic polymers known for hair treatment and hair setting agents have the disadvantage, in particular in formulations with anionic surfactants, that the hair-activating and hair-setting properties are gradually lost in the course of longer storage times. It was therefore proposed in DE-OS 37 08 451, zwitterionic polymers consisting of 30-70% monomers with quaternary ammonium groups, 10-30% monomeric olefinically unsaturated carboxylic acids, 10-30% monomeric olefinically unsaturated carboxylic acid esters and 0-40% monomers with tertiary amino groups to use. These polymers are well tolerated with anionic and cationic surfactants and show good hair-activating and hair-stabilizing properties.
  • Suitable polymers are thus available to achieve the desired effects on the hair, but these are composed of at least 3 or 4 monomers. There is therefore still a need for polymers which, with comparable properties, have a less complex structure, ie can be prepared from a smaller number of different monomers.
  • the invention thus relates to aqueous preparations for hair treatment containing zwitterionic polymers, characterized in that the zwitterionic polymers essentially consist of one another
  • R 1 -CH CR 2 -CO-Z- (C n H 2n ) -N (+) R 3 R 4 R 5 A (-) (I) in which R 1 and R 2 independently of one another represent hydrogen or a Methyl group and R 3 , R 4 and R 5 independently of one another for alkyl groups with 1 to 4 carbon atoms, Z an NH group or an oxygen atom, n an integer from 2 to 5 and A (-) the anion of an organic or inorganic Acid is and
  • R 6 -CH CR 7 -COOH (II) in which R 6 and R 7 are independently hydrogen or methyl groups.
  • Suitable starting monomers are e.g. B. dimethylaminoethyl acrylamide, dimethylaminoethyl methacrylamide, dimethylaminopropyl acrylamide, dimethylaminopropyl methacrylamide and diethylaminoethyl acrylamide if Z represents an NH group or dimethylaminoethyl acrylate, dimethylaminoethyl methacrylate and diethylaminoethyl acrylate if Z is an oxygen atom.
  • the monomers mentioned are prepared by known processes, such as those described in, for. B. in US-PS 3 878 247, DE-PS 28 19 735, DE-PS 28 36 520, DE-PS 34 02 599 or CH-PS 464 891 are described.
  • the monomers containing a tertiary amino group are then quaternized in a known manner, methyl chloride, dimethyl sulfate or diethyl sulfate being particularly suitable as alkylating reagents.
  • the quaternization reaction can be carried out in aqueous solution or in the solvent. Suitable methods are e.g. B. in DE-OS 3330326, DE-OS 2537378 or DE-OS 3244274 described.
  • Monomers of the formula (I) which are derivatives of acrylamide or methacrylamide are advantageously used. Also preferred are those monomers which contain halide, methoxysulfate or ethoxysulfate ions as counterions. Monomers of the formula (I) in which R 3 , R 4 and R 5 are methyl groups are also preferred.
  • Acrylamidopropyltrimethylammonium chloride is a very particularly preferred monomer of formula (I).
  • Acrylic acid, methacrylic acid, crotonic acid and 2-methyl-crotonic acid are suitable as monomeric carboxylic acids of formula (II).
  • the zwitterionic polymers according to the invention are prepared from monomers of the formulas (I) and (II) by polymerization processes known per se.
  • the polymerization can take place in either an aqueous or aqueous-alcoholic solution. Alcohols with 1 to 4 carbon atoms, preferably isopropanol, are used as alcohols, which simultaneously serve as polymerization regulators. However, other components can also be added to the monomer solution as regulators, e.g. B. formic acid or mercaptans such as thioethanol and thioglycolic acid.
  • the polymerization is initiated with the help of radical-forming substances. For this purpose, redox systems and / or thermally decomposing radical formers of the type of azo compounds, such as.
  • B azoisobutyronitrile, azo-bis (cyanopentanoic acid) or azo-bis (amidinopropane) dihydrochloride can be used.
  • redox systems such.
  • the polymerization can be carried out isothermally or under adiabatic conditions, the temperature range for the course of the reaction being able to fluctuate between 20 and 200 ° C. depending on the concentration ratios as a result of the heat of polymerization being released, and the reaction may have to be carried out under the excess pressure which arises.
  • the reaction temperature is preferably between 20 and 100.degree.
  • the pH during the copolymerization can vary within a wide range. Polymerization is advantageously carried out at low pH values; however, pH values above the neutral point are also possible.
  • an aqueous base e.g. As sodium hydroxide solution, potassium hydroxide solution or ammonia, adjusted to a pH between 5 and 10, preferably 6 to 8. Further information on the polymerization process can be found in the examples.
  • Polymers in which the monomers of the formula (I) were in excess of the monomers of the formula (II) have proven to be particularly effective. It is therefore preferred according to the invention to use those polymers which consist of monomers of the formula (I) and the monomers of the formula (II) in a molar ratio of from 60:40 to 95: 5, in particular from 75:25 to 95: 5 .
  • the zwitterionic polymers mentioned are preferably present in the preparations according to the invention in amounts of 0.1 to 10% by weight, based on the entire preparation.
  • the wet combability-improving effect of the polymers is very great even at low concentrations; the hair-activating and hair-setting effects, in contrast, are observed in most cases only at concentrations above about 1% by weight. It is therefore particularly preferred to use the polymers in amounts of about 1 to 5% by weight.
  • the zwitterionic polymers according to the invention are preferably used in aqueous preparations containing surface-active compounds.
  • Anionic, zwitterionic, amphoteric and / or nonionic surfactants are preferred as surface-active compounds.
  • Suitable anionic surfactants in hair treatment compositions according to the invention are all anionic surface-active substances suitable for use on the human body. These are characterized by a water-solubilizing, anionic group such as. B. a carboxylate, sulfate, sulfonate or phosphate group and a lipophilic alkyl group with about 10 to 22 carbon atoms.
  • the molecule can contain glycol or polyglycol ether groups, ester, ether and amide groups and hydroxyl groups.
  • suitable anionic surfactants are the sodium, potassium and ammonium and the mono-, di- and trialkanolammonium salts with 2 or 3 carbon atoms in the alkanol group, from
  • Preferred anionic surfactants are alkyl sulfate and alkyl polyglycol ether sulfates with 10 to 18 carbon atoms in the alkyl group and up to 12 glycol ether groups in the molecule.
  • Zwitterionic surfactants are surface-active compounds that contain at least one quaternary ammonium group and at least one -COO (-) - or -SO 3 (-) - group in the molecule.
  • Particularly suitable zwitterionic surfactants are the so-called betaines such as the N-alkyl-N, N-dimethylammonium glycinate, for example the coconut alkyl-N, N-dimethylammonium glycinate, N-acyl-aminopropyl-N, N-dimethylammonium glycinate, for example the cocoacylaminopropyl N, N-dimethylammonium glycinate, and 2-alkyl3-carboxylmethyl-3-hydroxyethyl-imidazolines each having 8 to 18 carbon atoms in the alkyl or acyl group, as well as the cocoacylaminoethylhydroxyethylcarboxymethylglycinate.
  • Amphoteric surfactants are surface-active compounds which, in addition to a C 8 -C 18 alkyl or acyl group, contain at least one free amino group and at least one --COOH or -SO 3 H group in the molecule and are capable of forming internal salts are.
  • amphoteric surfactants are N-alkylglycine, N-alkylaminopropionic acid, N-alkylaminobutyric acid, N-alkyliminodipropionic acid, N-hydroxyethyl-N-alkylamidopropylglycine, N-alkyltaurine, N-alkyl sarcosine, 2-alkyl aminopropionic acids and alkylaminoacetic acids each having about 8 to 18 carbon atoms in the alkyl group.
  • Nonionic surfactants are, above all, the addition products of 2 to 20 moles of ethylene oxide with preferably linear alcohols with 12 to 18 C atoms, with alkylphenols with 8 to 15 C atoms in the alkyl group, with fatty acids with 12 to 18 C atoms, with fatty acid partial glycerides , on fatty acid sorbitan partial esters, on fatty acid alkanolamides and on methyl glucoside fatty acid esters.
  • Other suitable nonionic surfactants are alkyl (oligo) glucosides, alkylamine oxide surfactants and fatty acid alkanolamides.
  • Cationic surfactants can also be present in the preparations according to the invention if they are combined with the other components, e.g. anionic surfactants are compatible.
  • Such cationic surfactants are e.g. B. from DE-OS 3442175 known.
  • the preparations according to the invention preferably contain surface-active compounds in amounts of 0.1 to 40% by weight, based on the entire preparation.
  • the zwitterionic polymers according to the invention are suitable as a setting and hair-activating component in all common aqueous preparations for cleaning and care of the hair.
  • Such preparations can e.g. B. hair shampoos, hair rinsing agents, hair setting agents, hair blow agents and aqueous colorants, permanent waving agents or permanent wave fixing agents.
  • the aqueous preparations for cleaning and maintaining the hair according to the invention can therefore contain, in addition to the obligatory zwitterionic polymers, all auxiliaries and additives customary for the particular application.
  • cationic surfactants especially surface-active quaternary ammonium salts, fatty alcohols with 12 to 22 carbon atoms, fatty acid partial glycerides, cosmetic oil and fat components and water-soluble polymers with thickening effect.
  • cationic surfactants especially surface-active quaternary ammonium salts, fatty alcohols with 12 to 22 carbon atoms, fatty acid partial glycerides, cosmetic oil and fat components and water-soluble polymers with thickening effect.
  • hair fixers and blow dryers these are e.g. B. also cationic surfactants, cationic, nonionic or anionic polymers and lower alcohols.
  • Hair dyes contain direct dyes or oxidation dye precursors, anionic or non-ionic surfactants, ammonia or alkanolamines and possibly antioxidants.
  • Permanent wave fixatives contain an oxidizing agent, e.g. B. H 2 O 2 , H 2 O 2 addition compounds or potassium bromate, and anionic or nonionic sur
  • the preparations according to the invention preferably have a pH of 4 to 10, in particular 5 to 9.
  • the rinse is in the form of a cloudy solution.
  • the wet combability of hair treated with this conditioner was very good; hair stress or static electricity was not observed. 2.2. Hair conditioner No.2
  • the rinse is in the form of a cloudy solution.
  • the wet combability of hair treated with this conditioner was very good.
  • the rinse is in the form of an almost clear solution.
  • the wet combability of hair treated with this conditioner was very good.
  • the wet combability of the hair shampooed with this preparation was excellent.
  • Texapon (R) K14 S spec. 15.0 sulfosuccinic acid half- esters based on a C 12-14 alkyl polyglycol (3 EO) ether, disodium salt (40%
  • n-alkyl (C 12-14 ), (50% active substance) (HORIZON)
  • the shampoo is clear and colorless. When the hair was treated with this shampoo, it received an excellent finish.
  • This clear shampoo was particularly characterized by an excellent conditioning effect with good cleaning performance.

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  • Life Sciences & Earth Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Birds (AREA)
  • Epidemiology (AREA)
  • Cosmetics (AREA)

Abstract

Des préparations aqueuses pour soins capillaires renfermant des polymérisats de zwitterion et composées essentiellement de A) monomères contenant des groupes ammonium quaternaires de formule générale (I): R1-CH=CR2-CO-Z-(CnH2n)-N(+)R3R4R5 A(-), où R1 et R2 représentent indépendamment hydrogène ou un groupe méthyle et R3, R4 et R5 représentent indépendamment des groupes alkyle avec 1 à 4 atomes de carbone, Z représente un groupe NH ou un atome d'oxygène, n est un entier compris entre 2 et 5 et A(-) est un anion d'un acide organique ou inorganique, et B) d'acides carboxyliques monomères de formule générale (II): R6-CH=CR7-COOH, où R6 et R7 représentent indépendamment hydrogène ou des groupes méthyle, permettent de raviver les cheveux et de fixer la coiffure. Des cheveux mouillés traités avec ces préparations se coiffent aussi aisément que ceux traités avec des rinçages cationiques.
PCT/EP1990/001444 1989-09-08 1990-08-30 Preparations pour soins capillaires WO1991003229A1 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DEP3929973.2 1989-09-08
DE19893929973 DE3929973A1 (de) 1989-09-08 1989-09-08 Haarpflegemittel

Publications (1)

Publication Number Publication Date
WO1991003229A1 true WO1991003229A1 (fr) 1991-03-21

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Application Number Title Priority Date Filing Date
PCT/EP1990/001444 WO1991003229A1 (fr) 1989-09-08 1990-08-30 Preparations pour soins capillaires

Country Status (6)

Country Link
EP (1) EP0490982A1 (fr)
JP (1) JPH05500220A (fr)
CA (1) CA2066226A1 (fr)
DD (1) DD297554A5 (fr)
DE (1) DE3929973A1 (fr)
WO (1) WO1991003229A1 (fr)

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1993005756A1 (fr) * 1991-09-25 1993-04-01 Henkel Kommanditgesellschaft Auf Aktien Preparations pour le traitement des cheveux
WO1994001076A1 (fr) * 1992-07-03 1994-01-20 Henkel Kommanditgesellschaft Auf Aktien Agent de traitement capillaire
WO1994001077A1 (fr) * 1992-07-03 1994-01-20 Henkel Kommanditgesellschaft Auf Aktien Agents de traitement capillaire
US5631003A (en) * 1991-09-25 1997-05-20 Henkel Kommanditgesellschaft Auf Aktien Hair treatment prepartation
US6555101B1 (en) * 1992-09-29 2003-04-29 Henkel Kommanditgesellschaft Auf Aktien Hair aftertreatment preparations
US6555100B1 (en) 1997-12-31 2003-04-29 L'ORéAL S.A. Compositions for treating keratinous materials containing a combination of a zwitterion polymer and a water insoluble non-volatile silicon
US7553338B2 (en) 2004-09-16 2009-06-30 Henkel Kgaa Color-modifying compositions containing a moringa plant seed protein and methods of treating keratin fibers therewith

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FR2833832B1 (fr) † 2001-12-21 2005-08-05 Oreal Composition pour la teinture d'oxydation des fibres keratiniques comprenant un acide ether carboxylique oxyalkylene, un tensioactif non-ionique et un polymere particulier
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DE102007045974A1 (de) 2007-09-25 2009-04-09 Henkel Ag & Co. Kgaa Biotin und Kieselsäure gegen Haaralterung
DE102007046628A1 (de) 2007-09-27 2009-04-02 Henkel Ag & Co. Kgaa Haarfärbeverfahren mit oxidativer Vorbehandlung
DE102007048140A1 (de) 2007-10-05 2009-04-09 Henkel Ag & Co. Kgaa Oxidative Haarbehandlung mit verringerter Haarschädigung
DE102007050767B4 (de) 2007-10-22 2013-10-02 Henkel Ag & Co. Kgaa Mund- und Zahnpflege- und reinigungsmittel, enthaltend 2- und/oder 3- und/oder 4-Piperidon und Verwendung dieser Piperidone
DE102007053952A1 (de) 2007-11-09 2009-05-14 Henkel Ag & Co. Kgaa Mittel enthaltend Esterverbindung mit Wachsalkoholkomponente
DE102008038138A1 (de) 2008-08-18 2010-02-25 Henkel Ag & Co. Kgaa Farbige Haarbehandlungsmittel
DE102007053950A1 (de) 2007-11-09 2009-05-14 Henkel Ag & Co. Kgaa Mittel mit Bioflavonoid
DE102008014368A1 (de) 2008-03-17 2009-10-08 Henkel Ag & Co. Kgaa Haarbehandlungsmittel mit Tilirosid und Vitamin B
DE102007054708A1 (de) 2007-11-14 2009-05-20 Henkel Ag & Co. Kgaa Haarbehandlungsmittel mit Litchi-Extrakt und Imidazolderivaten
DE102007054706A1 (de) 2007-11-14 2009-05-20 Henkel Ag & Co. Kgaa Haarbehandlungsmittel mit Litchi Extrakt und Taurin
DE102007056934A1 (de) 2007-11-23 2009-05-28 Henkel Ag & Co. Kgaa Oxidationsfärbemittel zur Färbung keratinhaltiger Fasern mit Luftsauerstoff als einzigem Oxidationsmittel
DE102008034386A1 (de) 2007-11-23 2009-07-30 Henkel Ag & Co. Kgaa Proteinhydrolysate und deren Derivate sowie Mittel, enthaltend diese
DE102007056935A1 (de) 2007-11-23 2009-05-28 Henkel Ag & Co. Kgaa Zweikomponenten Aerosolhaarfarbe
DE102007060528A1 (de) 2007-12-13 2009-06-18 Henkel Ag & Co. Kgaa Haarkonditionierende Mittel mit Imidazolinen und ausgewählten Siliconen und/oder kosmetischen Ölen
DE102007060532A1 (de) 2007-12-13 2009-09-17 Henkel Ag & Co. Kgaa Haarkonditionierende Mittel mit kationischen Verbindungen und ausgewählten Siliconen und/oder kosmetischen Ölen
DE102007060530A1 (de) 2007-12-13 2009-09-17 Henkel Ag & Co. Kgaa Haarkonditionierende Mittel mit kationischen Behenylverbindungen und ausgewählten Siliconen und/oder kosmetischen Ölen
DE102009009004A1 (de) 2008-02-18 2009-09-17 Seaquist Perfect Dispensing Gmbh Abgabevorrichtung mit einem kosmetischen Fluid
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DE102008012068A1 (de) 2008-02-29 2009-09-10 Henkel Ag & Co. Kgaa Haarbehandlungsmittel mit Cranberry-Extrakt
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DE102008019340A1 (de) 2008-04-16 2009-10-22 Henkel Ag & Co. Kgaa Haarbehandlungsmittel mit Cloudberry-Fruchtextrakt
DE102008031701A1 (de) 2008-07-04 2010-01-07 Henkel Ag & Co. Kgaa Haarkonditionierende Mittel mit Imidazolinen
DE102008031749A1 (de) 2008-07-04 2010-01-07 Henkel Ag & Co. Kgaa Haarkonditionierende Mittel mit Imidazolinen
DE102008031726A1 (de) 2008-07-04 2010-01-07 Henkel Ag & Co. Kgaa Haarkonditionierende Mittel mit Imidazolinen
DE102008031748A1 (de) 2008-07-04 2010-01-07 Henkel Ag & Co. Kgaa Haarkonditionierende Mittel mit Imidazolinen
DE102008031700A1 (de) 2008-07-04 2010-01-07 Henkel Ag & Co. Kgaa Haarkonditionierende Mittel mit Imidazolinen
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DE102008031702A1 (de) 2008-07-04 2010-01-07 Henkel Ag & Co. Kgaa Haarkonditionierende Mittel mit Imidazolinen
DE102008032208A1 (de) 2008-07-09 2010-01-14 Henkel Ag & Co. Kgaa Oxidationsfärbemittel mit basischer Aminosäure, Ammoniumsulfat und Alkanolaminen
DE102008032179A1 (de) 2008-07-09 2010-01-21 Henkel Ag & Co. Kgaa Rinse-off-Produkte mit Benefit-Wirkung auf die Haut
DE102008034388A1 (de) 2008-07-23 2010-01-28 Henkel Ag & Co. Kgaa Tensidhaltige Zusammensetzung mit spezieller Emulgatormischung
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DE102008036952A1 (de) 2008-08-08 2009-06-10 Henkel Ag & Co. Kgaa Blondiermittel mit Mischungsindikation
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DE102008046178A1 (de) 2008-09-06 2010-03-11 Henkel Ag & Co. Kgaa Kosmetische Zusammensetzung enthaltend ein Öl aus den Früchten, insbesondere den Kernen von Pflanzen der Ordnung Rosales
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DE102008063280A1 (de) 2008-12-29 2010-07-01 Henkel Ag & Co. Kgaa Wellmittel mit Aloe Vera
DE102009026775A1 (de) 2009-06-05 2010-12-09 Henkel Ag & Co. Kgaa Tensidhaltiges kosmetisches Reinigungsmittel mit Gelee Royale
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DE102009028443A1 (de) 2009-08-11 2010-06-10 Henkel Ag & Co. Kgaa Tensidhaltiges kosmetisches Haarreinigungsmittel mit Pentaclethra Macroloba Seed Oil
DE102009029183A1 (de) 2009-09-03 2011-03-10 Henkel Ag & Co. Kgaa Dauerwellsystem
DE102009044920A1 (de) 2009-09-23 2011-04-07 Henkel Ag & Co. Kgaa Verwendung bestimmter Aminosäuren in Färbemitteln keratinischer Fasern zur Farbintensivierung
DE102009045176A1 (de) 2009-09-30 2011-04-07 Henkel Ag & Co. Kgaa Wärmeunterstützende reduktive Entfärbung keratinhaltiger Fasern
DE102009045606A1 (de) 2009-10-13 2011-04-14 Henkel Ag & Co. Kgaa Sensitives Haarreinigungsmittel
DE102009045605A1 (de) 2009-10-13 2011-04-14 Henkel Ag & Co. Kgaa Versprühbares Haarreinigungsmittel
DE102010001360A1 (de) 2009-11-18 2011-05-19 Henkel Ag & Co. Kgaa Schaumförmige Färbemittel
WO2011061144A2 (fr) 2009-11-20 2011-05-26 Basf Se Utilisation de bêta-(1,3)-bêta-(1,4)-glucane ayant une masse moléculaire moyenne de 5 000 à 150 000 da pour augmentation de synthèse du collagène
DE102010002558A1 (de) 2009-11-20 2011-06-01 Symrise Ag Verwendung physiologischer Kühlwirkstoffe und Mittel enthaltend solche Wirkstoffe
DE102009054833A1 (de) 2009-12-17 2011-06-22 Henkel AG & Co. KGaA, 40589 Antibakterielle und bleichende Mund- und Zahnpflege- und -reinigungsmittel II
US8673275B2 (en) 2010-03-02 2014-03-18 Basf Se Block copolymers and their use
EP2542206B1 (fr) 2010-03-02 2015-05-13 Basf Se Copolymères en bloc et leurs utilisations
DE102010029976A1 (de) 2010-06-11 2011-12-15 Henkel Ag & Co. Kgaa Im wesentlichen Ammoniak freie Wellmittel
DE102010063518A1 (de) 2010-12-20 2012-06-21 Henkel Ag & Co. Kgaa Verfahren und Zusammensetzungen zur Glättung keratinhaltiger Fasern
DE102010055817A1 (de) 2010-12-23 2012-06-28 Henkel Ag & Co. Kgaa Treibmittelhaltige verschäumbare kosmetische Zusammensetzung zur Haut- und Körperpflege
EP3378313A1 (fr) 2011-03-23 2018-09-26 Basf Se Compositions contenant composés polymères ioniques comportant des groupes imidazolium
DE102011076852A1 (de) 2011-06-01 2012-12-06 Henkel Kgaa Im wesentlichen Ammoniak freie Wellmittel mit Cystein
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DE102016225377B4 (de) 2016-12-19 2022-04-28 Henkel Ag & Co. Kgaa Cremeförmiges Haarfärbemittel II
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CA3067664A1 (fr) 2017-06-26 2019-01-03 Basf Se Alcoxylation d'hydroxyacides
JP7231617B2 (ja) 2017-08-31 2023-03-01 ビーエーエスエフ ソシエタス・ヨーロピア 生理学的冷涼活性成分の使用、及びそのような活性成分を含む組成物
DE102018209894A1 (de) 2018-06-19 2019-12-19 Henkel Ag & Co. Kgaa Oxidatives Haaraufhell- oder Haarfärbemittel mit verbesserten Anwendungseigenschaften
DE102018209891A1 (de) 2018-06-19 2019-12-19 Henkel Ag & Co. Kgaa Oxidatives Haaraufhell- oder Haarfärbemittel aus Kaltherstellung für Level 2-Colorationen

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0047714A2 (fr) * 1980-09-05 1982-03-17 Ciba-Geigy Ag Mélanges de sels d'ammonium quaternaires, polymères, haut-moléculaires acryliques et de détergents, leur préparation et utilisation en formulations cosmétiques
GB2104091A (en) * 1981-07-17 1983-03-02 Kao Corp Detergent composition
EP0217274A2 (fr) * 1985-09-30 1987-04-08 Kao Corporation Composition cosmétique pour les cheveux
EP0283817A2 (fr) * 1987-03-16 1988-09-28 Henkel Kommanditgesellschaft auf Aktien Polymères zwittérioniques et leur utilisation dans des compositions de traitement de la chevelure

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CH645653A5 (de) * 1980-08-01 1984-10-15 Ciba Geigy Ag Quaternaere, copolymere, hochmolekulare ammoniumsalze auf acrylbasis, deren herstellung und verwendung als aktive komponente in kosmetischen mitteln.

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0047714A2 (fr) * 1980-09-05 1982-03-17 Ciba-Geigy Ag Mélanges de sels d'ammonium quaternaires, polymères, haut-moléculaires acryliques et de détergents, leur préparation et utilisation en formulations cosmétiques
GB2104091A (en) * 1981-07-17 1983-03-02 Kao Corp Detergent composition
EP0217274A2 (fr) * 1985-09-30 1987-04-08 Kao Corporation Composition cosmétique pour les cheveux
EP0283817A2 (fr) * 1987-03-16 1988-09-28 Henkel Kommanditgesellschaft auf Aktien Polymères zwittérioniques et leur utilisation dans des compositions de traitement de la chevelure

Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1993005756A1 (fr) * 1991-09-25 1993-04-01 Henkel Kommanditgesellschaft Auf Aktien Preparations pour le traitement des cheveux
EP0535447A1 (fr) * 1991-09-25 1993-04-07 Henkel KGaA Compositions pour le traitement des cheveux
US5631003A (en) * 1991-09-25 1997-05-20 Henkel Kommanditgesellschaft Auf Aktien Hair treatment prepartation
WO1994001076A1 (fr) * 1992-07-03 1994-01-20 Henkel Kommanditgesellschaft Auf Aktien Agent de traitement capillaire
WO1994001077A1 (fr) * 1992-07-03 1994-01-20 Henkel Kommanditgesellschaft Auf Aktien Agents de traitement capillaire
US6555101B1 (en) * 1992-09-29 2003-04-29 Henkel Kommanditgesellschaft Auf Aktien Hair aftertreatment preparations
US6555100B1 (en) 1997-12-31 2003-04-29 L'ORéAL S.A. Compositions for treating keratinous materials containing a combination of a zwitterion polymer and a water insoluble non-volatile silicon
EP0966248B2 (fr) † 1997-12-31 2008-04-02 L'oreal Compositions pour le traitement des matieres keratiniques contenant l'association d'un polymere zwitterionique et d'une silicone non-volatile et insoluble dans l'eau
US7553338B2 (en) 2004-09-16 2009-06-30 Henkel Kgaa Color-modifying compositions containing a moringa plant seed protein and methods of treating keratin fibers therewith

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JPH05500220A (ja) 1993-01-21
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CA2066226A1 (fr) 1991-03-09
DD297554A5 (de) 1992-01-16

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