Basf Aktiengesellschaft

Basfaktiengesellschaft

Franz Frosch

Axel Sanner

Horst Westenfelder

Hans-Juergen Raubenheimer

Hans-Ulrich Wekel

Harald Meyer

Christian Schade

Friedrich Vogel

Hans J Richter

Walter Denzinger

Knut Oppenlaender

Birgit Potthoff-Karl

Karl Stork

Hans-Helmut Goertz

Paul Naegele

Ferdinand Straub

Karin Sperling-Vietmeier

Brigette Wegner

The use of copolymers obtainable by the radically initiated polymerization of A) 50 to 99.9 wt % of an olefinically unsaturated C3 to C5 monocarboxylic acid, an olefinically unsaturated C4 to C8 dicarboxylic acid or its anhydride, or a mixture of such carboxylic acids or carboxylic acid anhydrides with B) 0.1 to 50 wt % of one or more long-chained compounds with isolated multiple C&#x2014;C bonds from the group (1) mono or polyunsaturated C8 to C30 monocarboxylic acids which may have additional hydroxyl groups and their alkaline metal and earth alkaline metal salts, alkyl esters, amides, sorbitane esters, glycerin esters and polyglycerin esters, (2) mono or polyunsaturated aliphatic Ca to C30 amines, (3) mono or polyunsaturated C8 to C30 alcohols and esters thereof with saturated Cl to C4 monocarboxylic acids, (4) to (C8 to C30 alkyl) vinyl ether which may incorporate up to 25 alkylene oxide units, and (5) final and medium-position Ci3 to C30 alkenes; C) 0 to 49.9 wt % of other copolymerizable monomers, and D) 0 to 10 wt % of one or more compounds with at least two olefinically unsaturated groups in the molecule as cross-linking agents, as thickening or dispersing agents, especially in cosmetic and pharmaceutical preparations.

Use of copolymers of carboxylic acids and long-chain compounds with isolated C-C multiple bonds as thickeners or dispersants

Copolymers of carboxylic acids and quaternary ammonium compounds and the use thereof as thickeners of dispersants

Stabilization of copolymers of maleic acid or maleic anhydride and vinyl

Copolymers which contain a) from 2 to 50 mol % of vinyl alkyl ethers having 3 to 30 carbon atoms in the molecule, b) from 10 to 88 mol % of monoethylenically unsaturated dicarboxylic anhydrides and c) from 10 to 88 mol % of dialkyl esters of monoethylenically unsaturated dicarboxylic acids as typical monomer units in polymerized form are prepared by copolymerizing the monomers a), b) and c) at from 40.degree. to 180.degree. C. in the presence of free radical initiators and are used as film-forming resins in hair sprays and, in the form of the alkali metal, ammonium or alkaline earth metal salts, as thickeners for aqueous systems, such as cosmetic and pharmaceutical formulations, textile print pastes, liquid detergents and cleaning agents.

Copolymers based on vinyl ethers and monoethylenically unsaturated

A terpolymer suitable for use as a film former in hair setting compositions is obtainable by free radical polymerization of 10%-24% by weight of N-vinylpyrrolidone, 46%-74% by weight of tert-butyl acrylate or methacrylate and 16%-30% by weight of acrylic or methacrylic acid, whose carboxyl groups may be partially or completely neutralized with an organic amine, ammonia or a basic alkali metal compound and which has a K value of from 25 to 65.

Terpolymers, use thereof in hair setting compositions for increased

Copolymers of monoalkyl maleates or maleic acid and salts thereof and vinyl alkyl ethers are prepared by free radical copolymerization of maleic anhydride and vinyl alkyl ethers and subsequent reaction with an alkanol or water and optionally metal hydroxides and/or oxides in a process wherein at every stage of the polymerization the vinyl alkyl ether component is present in excess in the reaction mixture, the free radical copolymerization is carried out in acetone and the acetone is removed by distillation during or after the esterification or hydrolysis, which comprises using a peroxyester of a carboxylic acid of 8 or more carbon atoms as polymerization initiator. The copolymers obtained are used in cosmetic preparations.

Preparation of copolymers of monoalkyl maleates or maleic acid and salts

Copolymers selectively hydrogenated on the olefinic double bond and composed of

Use of selectively hydrogenated styrene/butadiene copolymers in cosmetic

Mixtures of polyglycerol fatty esters obtainable by partial esterification of a polyglycerol mixture consisting of

Use of mixtures of polyglycerol fatty esters as emulsifiers in cosmetic

Copolymers of monoalkyl maleates and vinyl alkyl ethers are prepared by free radical copolymerization of maleic anhydride and a vinyl alkyl ether followed by reaction with an alkanol, by a process in which the vinyl alkyl ether component is present in excess in the reaction mixture in each phase of the polymerization, the free radical copolymerization is carried out in acetone and the acetone is removed by distillation during or after ester formation at up to 70.degree. C.

Preparation of copolymers of monoalkyl maleates and vinyl alkyl ethers

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Bad Durkheim, Germany

Franz Frosch