Basf Aktiengesellschaft

Basf Se Corporation

Peter Spang

Peter Neumann

Hubert Trauth

Gerhard Wagenblast

Werner Bertleff

Alexander Aumueller

Richard Baur

Dietmar Posselt

Marc Walter

Harald Schwahn

Andreas Daiss

Helmut Meffert

Stefan Hirsch

Frank-Olaf Mähling

Michael Kerber

Andreas Bauder

Guenter Matzke

Marcos Gomez

Irene Trötsch-Schaller

Erich K Fehr

Stephan Hoffmann

Siegfried Willert

Matthias Frohberger

Peter SCHÄFFLER

Incorporation of crosslinked polyvinylpyrrolidone in a specific particle composition as a disintegrant in compact particulate laundry detergents or cleaning products, such a particle composition and the compact particulate laundry detergents themselves, a process for preparing such a compact particulate laundry detergents or cleaning products, and a process for preparing specific particle compositions.

Use of cross-linked polyvinylpyrrolidone as a disintegrant in compact, particulate detergents and cleaning agents

The particle size of popcorn polymers is established during the popcorn polymerization by a process in which reaction mixtures forming popcorn polymers and comprising monoethylenically unsaturated monomers and a crosslinking agent are polymerized in the absence of oxygen and polymerization initiators at up to 200&deg; C. and in which the popcorn polymerization is carried out as a precipitation polymerization in water or in the absence of a solvent and the particle size of the popcorn polymers is controlled in the range from 1 &mgr;m to 10 mm by passing an inert gas stream into the reaction mixture, and popcorn polymers having a mean particle diameter of from >400 &mgr;m to 1500 &mgr;m are used as beverage clarifiers, antidiarrheal drugs and disintegration accelerators for tablets.

Method for adjusting the particle size of popcorn polymers during popcorn polymerization

Heterocyclic amidine derivatives of the general formula I ##STR1## in which the variables R.sup.1 are the same or different and denote hydrogen, C.sub.1 -C.sub.4 -alkyl, C.sub.1 -C.sub.4 -alkoxy, hydroxyl or chlorine,

Heterocyclic amidine derivatives

The preparation of 2-cyano-3,3-diarylacrylates I ##STR1## (in which Ar.sup.1 and Ar.sup.2 are aromatic radicals and R is an aliphatic radical having from 3 to 30 carbon atoms) by reacting a 2-cyano-3,3-diarylacrylate II ##STR2## (in which R.sup.1 is methyl or ethyl) with an alcohol III

Process for the preparation of 2-cyano-3,3-diarylacrylates

Compounds of the general formula (I) ##STR1## where R.sup.1 and R.sup.2 are each H, Cl, alkyl, alkoxy, substituted or unsubstituted phenyl or phenylalkyl, R.sup.3 and R.sup.4 are each H, alkyl, oxaalkyl, alkoxy, oxaalkoxy, substituted or unsubstituted phenyl, phenylalkyl, phenoxy, phenylalkoxy, alkylcarbonylamino, benzoylamino, alkanoyloxy or benzoyloxy, n is 1 or 2 and R.sup.5 is -- when n is 1-alkyl, hydroxyalkyl, cycloalkyl, alkenyl, oxaalkyl, phenylalkyl or ##STR2## or -- when n is 2-akylene, cycloalkylene, alkenylene, oxaalkylene or ##STR3## where m is from 2 to 4, R.sup.6 is alkyl, alkenyl, cycloalkyl, phenylalkyl, substituted or unsubstituted phenyl or naphthyl, and R.sup.7 is alkylene, alkenylene, cycloalkylene, substituted or unsubstituted phenylene, naphthylene, diphenylene, ##STR4## are effective light stabilizers for organic materials, in particular for polymers.

N-substituted benzimidazole-2-carboxanilides

Benzimidazolecarboxanilides of the formula (I) ##STR1## where R.sup.1 and R.sup.2 are each H, Cl, alkyl, alkoxy, unsubstituted or alkyl-- or alkoxy-substituted phenyl or phenylalkyl, R.sup.3 and R.sup.4 are each H, uninterrupted or --O-- interrupted alkyl or alkoxy, unsubstituted or alkyl-- or alkoxy-substituted phenyl, phenylalkyl, phenoxy, phenylalkoxy, hydroxyalkyl, hydroxyalkoxy, alkylcarbonylamino, alkanoyloxy, benzoylamino or benzoyloxy, X is alkylene, n is 1 or 2 and where--if n is 1--R.sup.5 is Cl, --OR.sup.6 or --NR.sup.4 R.sup.8 or--if n is 2--R.sup.5 is --O--R.sup.12 --O-- or --N(R.sup.9)--R.sup.13 --N(R.sup.9 --where R.sup.6 is H, unsubstituted, OH-- or alkanoyloxy-substituted alkyl whose carbon chain may be interrupted by --O-- or --N(R.sup.9)--, cycloalkyl, alkenyl, phenylalkyl, phenoxyethyl, hydroxy alkyl, phenylhydroxyalkyl or glycidyl, R.sup.7 and R.sup.8 are H, alkyl, cycloalkyl, phenyl, naphthyl, alkenyl, phenylalkyl, hydroxyalkyl or --NR.sup.7 R.sup.8, a saturated 5- or 6-membered heterocycle, R.sup.9 is alkyl, cycloalkyl, alkenyl, phenyl, naphthyl or phenylalkyl, R.sup.12 is alkylene, alkenylene, cyclohexylene, oxaalkylene and R.sup.13 is alkylene, oxaalkylene, diphenylenemethane or dicyclohexylenemethane or --N(R.sup.9)--R.sup.13 --N(R.sup.9)- is piperazinylene, are excellent light stabilizers for organic materials such as polymers and coating binders.

Benzimidazole-2-carboxanilides

Benzimidazolecarboxanilides of the formula (I) ##STR1## where R.sup.1 and R.sup.2 are each H, Cl, alkyl, alkoxy, unsubstitued or alkyl- or alkoxy-substituted phenyl or phenylalkyl, R.sup.3 and R.sup.4 are each H, uninterrupted or --O-- interrupted alkyl or alkoxy, unsubstituted or alkyl- or alkoxy-substituted phenyl, phenylalkyl, phenoxy, phenylalkoxy hydroxyalkyl, hydroxyalkoxy, alkylcarbonylamino, alkanoyloxy, benzoylamino or benzoyloxy, X is alkylene, n is 1 or 2 and where--if n is 1--R.sup.5 is Cl, --OR.sup.6 or --NR.sup.7 R.sup.8 or--if n is 2--R.sup.5 is --O--R.sup.12 --O-- or --N(R.sup.9)--R.sup.13 --N(R.sup.9)-- where R.sup.6 is H, unsubstituted, OH-- or alkanoyloxy-substituted alkyl whose carbon chain may be interrupted by --O-- or --N(R.sup.9)--, cycloalkyl, alkenyl, phenylalkyl, phenoxyethyl, hydroxy alkyl, phenylhydroxyalkyl or glycidyl, R.sup.7 and R.sup.8 are H, alkyl, cycloalkyl, phenyl, naphthyl, alkenyl, phenylalkyl, hydroxyalkyl or --NR.sup.7 R.sup.8, a saturated 5- or 6- membered heterocycle, R.sup.9 is alkyl, cycloalkyl, alkenyl, phenyl, naphthyl or phenylalkyl, R.sup.12 is alkylene, alkenylene, cyclohexylene, oxaalkylene and R.sup.13 is alkylene, oxaalkylene, diphenylenemethane or dicyclohexylenemethane or --N(R.sup.9)--R.sup.13 --N(R.sup.9)-- is piperazinylene, are excellent light stabilizers for organic materials such as polymers and coating binders.

Benzimidazolecarboxanilides of the formula (I) ##STR1## where R.sup.1 and R.sup.2 independently of one another are each hydrogen, chlorine, bromine, alkyl, alkoxy, unsubstituted or alkyl-substituted or alkoxy-substituted phenyl or phenylalkyl, R.sup.3 and R.sup.4 independently of one another are each hydrogen, alkyl, alkyl which is interrupted by one or more oxygen atoms, alkoxy, alkoxy which is interrupted by one or more oxygen atoms, unsubstituted or alkyl-substituted or alkoxy-substituted phenyl, phenylalkoxy, alkanoylamino, benzoylamino, alkanoyloxy or benzoyloxy, n is 0, 1, 2, 3, 4 or 5, X is oxygen, ##STR2## R.sup.5 is hydrogen, alkyl, phenylalkyl, cyanomethyl, aminoethyl, hydroxyethyl, alkylcarbonyl or benzoyl, R.sup.6 is hydrogen, alkyl, phenylalkyl or phennyl and m is from 2 to 8, and the acid addition salts and hydrates of these compounds are stabilizers for organic material, in particular for plastics, such as polyethylene, polypropylene and polyamide.

2,6-polyalkylpiperidine-substituted benzimidazole-2-carboxanilides and

A mixture for stabilizing polyurethanes contains

Mixture for stabilizing polyurethanes

Photostabilized polymers, including polyurethanes and plastics coatings, contain as photostabilizer one or more compounds of the formula ##STR1## or a novel imidazole-2-carboxanilide of the formula ##STR2##

Growing community of inventors

St. Ingbert, Germany

Peter Spang