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
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
  • C08G18/00—Polymeric products of isocyanates or isothiocyanates
  • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
  • C08G18/08—Processes
  • C08G18/0804—Manufacture of polymers containing ionic or ionogenic groups
  • C08G18/0819—Manufacture of polymers containing ionic or ionogenic groups containing anionic or anionogenic groups
  • C08G18/0823—Manufacture of polymers containing ionic or ionogenic groups containing anionic or anionogenic groups containing carboxylate salt groups or groups forming them
• • 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
  • A61K8/87—Polyurethanes
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
  • A61Q19/00—Preparations for care of the skin
• • 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
  • A61Q5/06—Preparations for styling the hair, e.g. by temporary shaping or colouring
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
  • C08G18/00—Polymeric products of isocyanates or isothiocyanates
  • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
  • C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
  • C08G18/30—Low-molecular-weight compounds
  • C08G18/32—Polyhydroxy compounds; Polyamines; Hydroxyamines
  • C08G18/3271—Hydroxyamines
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
  • C08G18/00—Polymeric products of isocyanates or isothiocyanates
  • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
  • C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
  • C08G18/30—Low-molecular-weight compounds
  • C08G18/34—Carboxylic acids; Esters thereof with monohydroxyl compounds
  • C08G18/348—Hydroxycarboxylic acids
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
  • C08G18/00—Polymeric products of isocyanates or isothiocyanates
  • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
  • C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
  • C08G18/40—High-molecular-weight compounds
  • C08G18/58—Epoxy resins

Definitions

• the invention relates to a cosmetic or personal care composition
• a cosmetic or personal care composition comprising a polymer which polymer comprises oxazolidon groups.
• cosmetic and personal care compositions include hair spray compositions, mousses, gels, lotions, tonics, shampoos, conditioners, rinses, hand and body lotions, facial moisturizers, sunscreens, anti-acne preparations, topical analgesics, mascara's, eyeliners, blush, liquid lip color, nail polish and foundations.
• a hair care product for example must meet a variety of requirements including exhibiting fine spray pattern, good film formation, good holding power, prolonged curl retention, low stickiness, lack of powdering or flaking, being clear, transparent and glossy and easy to remove upon washing the hair with shampoo or soap. Lately it has become especially desirable to provide a high level of style retention, or strong hold, from a hair care product.
• hair styling polymers also indicated by hair styling polymers.
• known hair styling polymers include copolymers of vinyl acetate and crotonic acid, copolymers of methyl vinyl ether and maleic anhydride, copolymers of acrylic acid or metacrylic acid with other monomers, polyurethanes, N-vinylpirrolidone and silicone polymers.
• polymers suitable for use in cosmetic compositions are polymers comprising oxazolidon groups in the main chain of the polymer. Such compositions show a good balance of properties, especially a high level of style retention is obtained as styling polymer in hair care compositions.
• the polymers comprising oxazolidon groups in the main chain show a good adhesion to skin and hair.
• the polymers comprising oxazolidon groups in the main chain are also suitable to be used as film formers in mascara, lip color, nail polish etc.
• the oxazolidon groups may further be present as side groups or in the side chains of the polymer.
• the oxazolidon group is suitably formed by the reaction of an epoxide and an isocyanate group.
• Such a polymer may suitably be formed from a reaction mixture comprising at least one epoxide functional compound and at least one isocyanate functional compound.
• the epoxide functional compound may contain one or more of epoxy, i.e. ⁇ , ⁇ -oxirane groups. It is preferred that the functionality of the epoxide functional compound is from 2 to 10, more preferably 2 to 4, and most preferably 2 to 3. Lower functionalities are preferred because they give rise to less highly branched polymers. Preferably diepoxides are used, which give rise to linear polymers when reacted with a diisocyanate.
• Monoepoxides may be used as chain stoppers.
• polyepoxides usefully employed herein are those represented by the general structure
• X is the residue of an active hydrogen-containing moiety after removal of said active hydrogen
• R′ is an organic mono- or polyradical and n is at least 1. n is preferably from 2 to 4 more preferably from 2 to 3.
• epoxide functional compounds are advantageously prepared by reacting a compound having a plurality of groups containing active hydrogen atoms with a halogen-containing oxirane such as epichlorohydrin or epibromohydrin.
• the group X is advantageously —O—, —NH—,
• R 2 is inertly substituted lower alkyl or phenyl.
• the group X is —O— and the epoxide functional compound is one prepared in the reaction of a polyhydroxyl containing compound with a halogenated oxirane as discussed hereinbefore.
• compounds according to structure I include epoxy terminated polyethylene glycol, epoxy terminated polypropylene glycol and epoxy terminated polytetrahydrofuran. Further suitable examples include diepoxides resulting from the reaction between epichorohydrin and ethylene glycole, diethylene glycol, neopentylglycol, respectively butane diol.
• epoxide functional compounds include epoxy-terminated derivatives of bisphenols, such as are represented by the structure (II)
• each A is independently a lower alkylene group such as methylene, ethylene, isopropylidine and the like, —O—, —S—,
• each B is as defined by A, and/or —OCH 2 CHOHCH 2 O—
• each R 5 is independently hydrogen, halogen or lower alkyl
• m is a number from 0 to 30, preferably 0 to 10 and more preferably 0.1 to 3.
• derivatives of the materials represented by structure (II) in which one or more of the positions on the group A is substituted with an inert substituent such as halogen, aryl, alkyl and the like are also useful herein.
• Suitable such epoxides include the commercially available resinous reaction products of an epihalohydrin with the diverse bisphenols and halogenated bisphenols, particularly the reaction products of an epihalohydrin with bisphenol A or bisphenol F or halogenated derivatives thereof.
• epoxy phenol novolac resins and epoxy cresol novolac resins which can be represented by the structure (III)
• n is for example a number from 0-20 and each R 3 is independently hydrogen, halogen, lower alkyl, aryl or aralkyl.
• aliphatic epoxy resins prepared in reaction of cycloolefins with peracetic acid, as well as diglycidyl ethers of cyclic dicarboxylic acids.
• isocyanate functional compounds preferably polyisocyanates, most preferably diisocyanates are used.
• Polyisocyanates which may be employed include aromatic, aliphatic and cycloaliphatic polyisocyanates and combinations thereof.
• diisocyanates such as m-phenylene diisocyanate, tolylene-2,4-diisocyanate, tolylene-2,6-diisocyanate, xylenediisocyanate, tetramethylxylene diisocyanate, isophorone diisocyanate, diphenyl methane diisocyanate, hydrogenated diphenyl methane diisocyanate, hydrogenated xylene diisocyanate, hexamethylene-1,6-diisocyanate, cyclohexane-1,4-diisocyanate, hexahydrotolylene diisocyanate (and isomers), naphthalene-1,5-diisocyanate, 1-methoxyphenyl-2,4-diisocyanate, diphenylmethane-4,4′-diisocyanate, 4,4′-biphenylene diisocyanate, 3,3′-d
• isocyanates are tolylene-2,4-diisocyanate, tolylene-2,6-diisocyanate, isophorone diisocyanate, diphenyl methane diisocyanate, hydrogenated diphenyl methane diisocyanate, hexamethylene-1,6-diisocyanate.
• a suitable process for the formation of oxazolidon groups is disclosed in U.S. Pat. No. 4,658,007.
• a process is disclosed wherein an epoxy functional compound and an isocyanate functional compound are reacted in the presence of an organo-antimony iodide catalyst.
• an organo-antimony iodide catalyst In general a reaction temperature between 80 and 180° C. is suitable.
• other catalysts such as secondary and tertiary amines, halide salts of amines, carboxylate anions, zinc chloride, ferric chloride, lithium chloride, lithium bromide or its complex with tributyl phosphineoxide can be used.
• the reaction may be carried out neat, but may also be carried out in the presence of a solvent.
• the relative proportions of the epoxy functional compound or the isocyanate functional compound employed, will control to a large extend the characteristics of the resulting oxazolidon polymer.
• Either the epoxy functional compound or the isocyanate functional compound can be used in excess.
• the use of an excess of an epoxy functional compound will result in the formation of epoxide terminated oxazolidon polymers.
• the use of an excess of an isocyanate functional compound will result in the formation of isocyanate terminated oxazolidon polymers.
• the molecular weight of the oxazolidon group comprising polymer will among other factors be determined by the epoxy:isocyante ratio.
• the number average molecular weight may be between 500 and 1.000.000, preferably between 1000 and 100.000 and most preferably between 1000 and 20.000.
• the oxazolidon group comprising polymer further comprises compounds to be incorporated in the oxazolidon group-comprising polymer, for example hydroxyl functional compounds and/or amine functional compounds.
• the oxazolidon group comprising polymer further comprises at least one hydroxyl functional compound and/or at least one amine functional compound.
• the polymer is formed in a process wherein in the first step the epoxy functional compound and the isocyanate functional compound are reacted to form a polyoxazolidon group containing polymer precursor and wherein in one or more further steps the polymer precursor is reacted with at least one of the further compounds, preferably at least one hydroxyl functional compound and or at least one amine functional compound. In this way the reaction condition for the formation of the oxazolidon groups can be better adapted.
• isocyanate terminated oxazolidon group comprising polymers it is possible to use hydroxyl and/or amine functional compounds as the further compounds.
• epoxy terminated oxazolidon group comprising polymers it is very well possible to use amine functional compounds as the further compounds.
• hydroxyl functional compounds monomeric or polymeric alcohols, diols or polyols may be used.
• Examples of monomeric alcohols include n-alkyl alcohols like methanol, ethanol propanol etc.
• polymeric alcohols include monomethoxy polyethylene glycol, monomethoxy polypropyleneglycol.
• Examples of monomeric diols include ethylene glycol, diethylene glycol, triethhylene glycol, propylene glycol, dipropylene glycol, propanediol, butanediol, neopentyl glycol, cyclohexanediol, cyclohexanedimethylol, bisfenol A, hydrogenated bisfenol A.
• polymeric diols examples include polyethylene gycol, polypropylene gycol, polytetrahydrofuran, polymethyl tetrahydrofuran, polybutadiene diol, hydrogenated polybutadiene diol, polyacrylate diol, aromatic or aliphatic polyester diol, ethoxylated bisfenol A at which de degree of ethoxylation is between 2 and 40, hydrogenated ethoxylated bisfenol A, polysiloxane diol and polycarbonate diol.
• monomeric polyols examples include trimethylol propane, trimethylol ethane, pentaerithritol.
• polymeric poyols examples include poly hydroxyl functional polyesters, polyacrylates, polysiloxanes.
• amine functional compounds monomeric or polymeric monoamine, diamine and polyamine compounds may be used.
• the amines may be primary or secondary amines.
• Examples include ethylamine, diethylamine, triethylamine, butane diamine, hexane diamine, isophorone diamine, amine functional polyethers, amine functional polytetrahydrofuran, amine functional polysiloxane.
• Preferred hydroxy functional compounds include amino alcohols. This is because these compounds provide improved water compatibility or solubility.
• suitable amino alcohols are 2-aminoethanol, 2-(N-methylamino) ethanol, 3-aminopropanol, 4-aminobutanol, 1-ethylaminobutan-2-ol, 2-amino-2-methyl-1-propanol, 4-methyl-4-aminopentan-2-ol etc.
• hydroxy or amine functional compounds include compounds having at least one ionogenic or ionic group per molecule, for example dimethyl di(2-hydroxyethyl)ammonium chloride or diethyl di(2-hydroxyethyl)ammonium chloride. More preferred hydroxy or amine functional compounds include compounds having at least one aniogenic or anionic group per molecule, for example compounds having carboxylate and/or sulfonate groups. This is because these compounds provide even further improved water compatibility or solubility. Particular preference is given to dimethylolpropanoic acid and mixtures comprising it.
• n and n independently of one another are an integer from 1 to 8, in particular from 1 to 6, and M is Li, Na or K.
• N—(C 1 -C 6 alkyl)diethanol amines such as for example methyl diethanol amine.
• cationic polymers may be obtained. These polymers are very suitable to be used in hair conditioners.
• suitable polymers are the polymers, used in cosmetic applications and comprising urethane groups, in which polymers at least an oxazolidon group has replaced a part of the urethane groups.
• the invention therefore also relates to a polymer comprising the reaction product of an isocyanate functional oxazolidon polymer and an amino alcohol.
• the invention also relates to a polymer comprising an oxazolidon group and a residue of an hydroxy and/or amino functional compound having at least one ionogenic or ionic group per molecule preferably at least one anionogenic or anionic group per molecule.
• the preparation of the cosmetic compositions according to the present invention is known to the skilled person.
• the amount of polymer in the composition will depend on its application and can easily be determined.
• additional components may be employed in cosmetic and personal care compositions according to the present invention.
• the additional components used in a particular composition will depend on kind of composition and its intended use and can therefore be selected by the skilled person. Examples of suitable additional components include
• compositions according to the invention may comprise water, alcohols, preferably ethanol, and dimethylether.
• composition according to the invention is a hair care composition.
• the invention also relates to a container comprising the composition according to the invention.
• the composition is brought into the market in all kind of containers, so that the consumer is able to store and use the composition.
• Suitable containers are for example bottles and pots, but also spray cans and siphons if for example the composition is a hair care composition.
• VOC was made by mixing: 10% polyoxazolidone-, -2 or -3 of example 1-3 55% ethanol 35% dimethylether
• a hair spray formulation with 80% VOC was made by mixing: 5% polyoxazolidone-1, -2 or -3 of example 1-3 45% ethanol 35% dimethylether 15% water
• a pump hair spray formulation with 55% VOC was made by mixing:
• the above-mentioned hairspray formulations are applied to a glass plates and the resulting films were tested for the following four criteria: Appearance, tackiness, smoothness and ease of washout with a surfactant solution.

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• Health & Medical Sciences (AREA)
• Chemical & Material Sciences (AREA)
• Life Sciences & Earth Sciences (AREA)
• Public Health (AREA)
• Animal Behavior & Ethology (AREA)
• Medicinal Chemistry (AREA)
• Polymers & Plastics (AREA)
• Organic Chemistry (AREA)
• Veterinary Medicine (AREA)
• General Health & Medical Sciences (AREA)
• Chemical Kinetics & Catalysis (AREA)
• Birds (AREA)
• Epidemiology (AREA)
• Manufacturing & Machinery (AREA)
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• Dermatology (AREA)
• Cosmetics (AREA)
• Polyurethanes Or Polyureas (AREA)

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• 2005
  • 2005-11-25 EP EP05077672A patent/EP1818044A1/de not_active Withdrawn
• 2006
  • 2006-11-27 CN CN2006800440467A patent/CN101312709B/zh not_active Expired - Fee Related
  • 2006-11-27 US US12/089,477 patent/US20080267898A1/en not_active Abandoned
  • 2006-11-27 EP EP06818850A patent/EP1951192B1/de not_active Not-in-force
  • 2006-11-27 JP JP2008541656A patent/JP5020965B2/ja not_active Expired - Fee Related
  • 2006-11-27 WO PCT/EP2006/011359 patent/WO2007060006A1/en active Application Filing
• 2008
  • 2008-05-23 KR KR1020087012314A patent/KR101343727B1/ko active IP Right Grant
• 2011
  • 2011-07-14 US US13/183,302 patent/US8268298B2/en not_active Expired - Fee Related

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