WO2013072155A2 - Produit de soins capillaires contenant des acides aminés et des silicones cationiques - Google Patents
Produit de soins capillaires contenant des acides aminés et des silicones cationiques Download PDFInfo
- Publication number
- WO2013072155A2 WO2013072155A2 PCT/EP2012/070660 EP2012070660W WO2013072155A2 WO 2013072155 A2 WO2013072155 A2 WO 2013072155A2 EP 2012070660 W EP2012070660 W EP 2012070660W WO 2013072155 A2 WO2013072155 A2 WO 2013072155A2
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- acid
- silicone quaternium
- polyquaternium
- cationic
- quaternium
- Prior art date
Links
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
- A61K8/84—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions otherwise than those involving only carbon-carbon unsaturated bonds
- A61K8/89—Polysiloxanes
- A61K8/896—Polysiloxanes containing atoms other than silicon, carbon, oxygen and hydrogen, e.g. dimethicone copolyol phosphate
- A61K8/898—Polysiloxanes containing atoms other than silicon, carbon, oxygen and hydrogen, e.g. dimethicone copolyol phosphate containing nitrogen, e.g. amodimethicone, trimethyl silyl amodimethicone or dimethicone propyl PG-betaine
-
- 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
- A61K8/40—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
- A61K8/442—Aminocarboxylic acids or derivatives thereof, e.g. aminocarboxylic acids containing sulfur; Salts; Esters or N-acylated derivatives thereof substituted by amido group(s)
-
- 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
- A61K8/466—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing sulfur containing sulfonic acid derivatives; Salts
-
- 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
- A61Q5/004—Preparations used to protect coloured hair
-
- 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
-
- 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
-
- 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
Definitions
- Hair treatment compositions in the context of the present invention are, for example, hair shampoos, hair conditioners, conditioning shampoos, hair conditioners, hair treatments, hair packs, hair tonics, hair dye shampoos or combinations thereof.
- the hair conditioning compositions such as hair conditioners, hair treatments, hair wraps, hair oils and lotions both as leave-on, so as on the hair until the next hair wash remaining products, as well as rinse-off, so few seconds to a few hours after Application again rinsed products, understood by the hair treatment compositions according to the invention.
- aryl or alkaryl radical for example phenyl or benzyl
- the cationic and / or amphoteric polymers may be homopolymers or copolymers or polymers based on natural polymers, wherein the quaternary nitrogen groups are contained either in the polymer chain or preferably as a substituent on one or more of the monomers.
- the ammonium group-containing monomers may be copolymerized with non-cationic monomers.
- Suitable cationic monomers are unsaturated, radically polymerizable compounds which carry at least one cationic group, in particular ammonium-substituted vinyl monomers such as, for example, trialkylmethacryloxyalkylammonium, trialkylacryloxyalkylammonium, dialkyldiallylammonium and quaternary
- R is a methyl group
- R 2 , R 3 and R 4 are methyl groups
- m is 2.
- Cationic, ie quaternized celluloses are available on the market with varying degrees of substitution, cationic charge density, nitrogen content and molecular weights.
- Polyquaternium-67 is commercially available under the designations SL ® polymer or polymer ® SK (Amerchol) is. Under the trade designation Mirustyle CP ® of the company. Croda another most preferred cellulose is available. This is a trimonium and cocodimonium hydroxyethylcellulose as derivatized cellulose with the INCI name Polyquaternium-72. Polyquaternium-72 can be used pre-dissolved both in solid form and already in aqueous solution.
- honey for example the commercial product Honeyquat ® 50,
- R 8 and R 9 are independently hydrogen or methyl groups.
- R 0 and R independently of one another are hydrogen or methyl groups and R 2 is a hydrogen atom or a (Cp to C 8 ) alkyl group.
- Amphoteric polymers based on a comonomer (Mono4) which are very particularly preferably used according to the invention are terpolymers of diallyldimethylammonium chloride, acrylamide and acrylic acid. These copolymers are marketed ® under the INCI name Polyquaternium-39, among others, with the trade name Merquat Plus 3330 (Nalco).
- radicals R are each independently a saturated or unsaturated, linear or branched hydrocarbon radical having a chain length of 8 to 30 carbon atoms and A is a physiologically acceptable anion, and / or
- Preferred ingredients of group c) are stearamidopropyldimethylamines and / or distearoylethyl hydroxyethylmonium methosulfates and / or dicocoyl hydroxyethylmonium methosulfates and / or dipalmitoylethyl dimonium chlorides and / or quaternium-27 and / or quaternium-91 and / or behenoyl PG -trimonium chlorides. Most preferably, it is further preferred to select at least two, more preferably at least three ingredients of this group. In these mixtures, it is most preferred for one of the two or three compounds to be stearamidopropyldimethylamine. It is most preferred, if further as an optional cationic ammonium compound cetyltrimethylammonium chloride or
- Behenyltrimethylammonium chloride is added.
- the dimethicones (Sil) are present in the compositions according to the invention in amounts of from 0.01 to 10% by weight, preferably from 0.01 to 8% by weight, particularly preferably from 0.1 to 7.5% by weight and in particular from 0.1 to 5 wt.% Based on the total composition.
- silicone compounds Dimethiconole (Si8) understood.
- the dimethiconols according to the invention can be both linear and branched as well as cyclic or cyclic and branched. Linear dimethiconols can be represented by the following structural formula (Si8-1):
- the dimethiconols (Si8) are present in the compositions according to the invention in amounts of from 0.01 to 10% by weight, preferably from 0.01 to 8% by weight, particularly preferably from 0.1 to 7.5% by weight and in particular from 0.1 to 5% by weight of dimethiconol based on the composition.
- Q according to formula (Si-2) is most preferably a polar amino-functional radical of formula - CH 2 CH 2 CH 2 NH 2 CH 2 CH 2 NH 2 .
- silicones are referred to as trimethylsilylamodimethicones according to the INCI declaration and are available, for example, under the name Q2-7224 (manufacturer: Dow Corning, a stabilized trimethylsilylamodimethicone).
- Alpha-sulfofatty acid methyl esters of fatty acids having 8 to 30 carbon atoms are alpha-sulfofatty acids having 8 to 30 carbon atoms.
- Examples of compounds of the formula (Tkat1) are lauryltrimethylammonium chloride, cetyltrimethylammonium chloride, cetyltrimethylammonium bromide, cetyltrimethylammonium methosulfate, dicetyldimethylammonium chloride, tricetylmethylammonium chloride, stearyltrimethylammonium chloride, distearyldimethylammonium chloride, lauryldimethylbenzylammonium chloride, behenyltrimethylammonium bromide, behenyltrimethylammonium bromide, behenyltrimethylammonium methosulfate.
- Decanols, octanols, dodecadienol, decadienol, oleyl alcohol, eruca alcohol, ricinoleic alcohol, stearyl alcohol, isostearyl alcohol, cetyl alcohol, lauryl alcohol, myristyl alcohol, arachidyl alcohol, caprylic alcohol, capric alcohol, linoleyl alcohol, linolenyl alcohol and behenyl alcohol are, for example, decanol, octanolol, dodecadienol, decadienol , as well as their Guerbet alcohols, this list should have exemplary and non-limiting character.
- Another subject of the invention is therefore a method for hair treatment, in which a hair treatment composition according to claim 1 is applied to the hair and is rinsed by the hair after a contact time.
- Coco Betaine 0.5 0.5 0.5 0.5 0.5 0.5 0.5 0.5 0.5 0.5 0.5 0.5 0.5 0.5 0.5 0.5 0.5 0.5 0.5 0.5 0.5 0.5 0.5 0.5
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Birds (AREA)
- Epidemiology (AREA)
- Dermatology (AREA)
- Cosmetics (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Abstract
L'invention concerne un produit de traitement capillaire contenant des acides aminés et des silicones cationiques. L'invention vise à réduire les effets secondaires dus aux actions de l'environnement et aux traitements capillaires oxydants et tensioactifs, de préférence déjà dès le traitement capillaire oxydant et tensioactif, mais également après le traitement capillaire oxydant et tensioactif, sans pour autant nuire à l'efficacité du cosmétique oxydant ou tensioactif, en particulier en termes d'intensité de la couleur, de solidité de la couleur, de pouvoir éclaircissant ou d'effet d'ondulation, ainsi qu'à empêcher le regraissage des fibres kératiniques et la multiplication de la formation de pellicules.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE102011086636.1 | 2011-11-18 | ||
DE201110086636 DE102011086636A1 (de) | 2011-11-18 | 2011-11-18 | Haarpflegemittel mit Aminosäuren und kationischen Silikonen |
Publications (2)
Publication Number | Publication Date |
---|---|
WO2013072155A2 true WO2013072155A2 (fr) | 2013-05-23 |
WO2013072155A3 WO2013072155A3 (fr) | 2014-04-03 |
Family
ID=47049166
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/EP2012/070660 WO2013072155A2 (fr) | 2011-11-18 | 2012-10-18 | Produit de soins capillaires contenant des acides aminés et des silicones cationiques |
Country Status (2)
Country | Link |
---|---|
DE (1) | DE102011086636A1 (fr) |
WO (1) | WO2013072155A2 (fr) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2013075892A3 (fr) * | 2011-11-23 | 2014-09-04 | Henkel Ag & Co. Kgaa | Produits de conditionnement capillaire |
EP2708263A3 (fr) * | 2012-09-13 | 2015-07-15 | Henkel AG&Co. KGAA | Produit de soin capillaire doté d'acides aminés sélectionnés et/ou d'oligopeptides sélectionnés et de tensioactifs cationiques végétaux sélectionnés |
US10982050B2 (en) * | 2019-04-25 | 2021-04-20 | Wuhan China Star Optoelectronics Semiconductor Display Technology Co., Ltd. | Sealing composite material, preparation method, and application thereof |
Family Cites Families (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6495498B2 (en) * | 1999-05-27 | 2002-12-17 | Johnson & Johnson Consumer Companies, Inc. | Detergent compositions with enhanced depositing, conditioning and softness capabilities |
WO2001001949A1 (fr) * | 1999-07-01 | 2001-01-11 | Johnson And Johnson Consumer Companies, Inc. | Compositions de nettoyage |
ITMI20070555A1 (it) * | 2007-03-21 | 2007-06-20 | Giuliani Spa | Composizione provvista di attivita' di inibizione sulla 5 alfa-reduttasi |
EP2005942A1 (fr) * | 2007-06-11 | 2008-12-24 | GIULIANI S.p.A. | Composition cosmétique pour le traitement de canities |
DE102009027964A1 (de) * | 2009-07-23 | 2011-01-27 | Henkel Ag & Co. Kgaa | Haarkonditionierende Mittel mit ausgewählten kationischen Siliconen und Dimethicon |
DE102009054493A1 (de) * | 2009-12-10 | 2011-06-16 | Henkel Ag & Co. Kgaa | Schonende Haarbehandlungsmittel zur Farbveränderung |
DE102010030654A1 (de) * | 2010-06-29 | 2011-01-05 | Lr Health And Beauty Systems Gmbh | Kosmetische Zusammensetzung auf der Basis von Aloe vera und deren Verwendung |
-
2011
- 2011-11-18 DE DE201110086636 patent/DE102011086636A1/de not_active Withdrawn
-
2012
- 2012-10-18 WO PCT/EP2012/070660 patent/WO2013072155A2/fr active Application Filing
Non-Patent Citations (1)
Title |
---|
"International Cosmetic Ingredient Dictionary and Handbook", 1997, THE COSMETIC, TOILETRY, AND FRAGRANCE ASSOCIATION |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2013075892A3 (fr) * | 2011-11-23 | 2014-09-04 | Henkel Ag & Co. Kgaa | Produits de conditionnement capillaire |
EP2708263A3 (fr) * | 2012-09-13 | 2015-07-15 | Henkel AG&Co. KGAA | Produit de soin capillaire doté d'acides aminés sélectionnés et/ou d'oligopeptides sélectionnés et de tensioactifs cationiques végétaux sélectionnés |
US10982050B2 (en) * | 2019-04-25 | 2021-04-20 | Wuhan China Star Optoelectronics Semiconductor Display Technology Co., Ltd. | Sealing composite material, preparation method, and application thereof |
Also Published As
Publication number | Publication date |
---|---|
WO2013072155A3 (fr) | 2014-04-03 |
DE102011086636A1 (de) | 2013-05-23 |
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