Henkel Kommanditgesellschaft Auf Aktien

Brigitte Hase

Bernd Wegemund

Joachim Galinke

Herbert Fischer

Wolfgang Gress

Ulrich Eicken

Norbert Stork

Hinrich Moller

Ulrich Zeidler

Christian Hase

Hans-Christoph Wilk

Horst-Juergen Krause

William E Fristad

Klaus Schumann

Paul Birnbrich

Manfred Gorzinski

Klaus-Dieter Wisotzki

Harald Frommelius

Gunther Konrad

Horst-Jurgen Krause

Konard Engelskirchen

Heinz-Guenter Schulte

Flow controllers for powder lacquers

Poly-N-acylalkyleneimines corresponding to the following formula ##STR1## are used as an oxidatively crosslinking constituent in paints. In formula (I), R--CO represents the acyl radical of a mono- or polyunsaturated, aliphatic C.sub.16-22 carboxylic acid or a mixture of such radicals, R'--CO represents the acyl radical of a C.sub.1-22 carboxylic acid or a mixture of such radicals and x and y represent the percentages by weight of the particular polymer units, x assuming values of 20 to 100% and preferably 20 to 95% and y assuming values of 80 to 0% and preferably 80 to 5%. The indices m and n independently of one another may assume the value 2 or 3.

New paint binders

Water-dilutable binder mixtures based on alkyd resins and poly-n-acyl

Coating process

Paint binders

This invention concerns polyiminoethers of general formula (I) in which A is an aliphatic, aromatic or araliphatic group containing 4 to 40 carbon atoms and n free valencies at various carbon atoms, x may assume values of 0 to 40, n has a value of 2, 3 or 4, Z is either a direct bond or the group CR.sup.5 R.sup.6, the substituents R.sup.1 to R.sup.6 independently of one another are H, alkyl or aryl containing up 8 carbon atoms, the substituent R.sup.7 is hydrogen, methyl or ethyl and Q is a phenylene group, which may be substituted by one or two methyl groups, or the group --CHR--M--, where R is selected from the group consisting of H, alkyl or alkenyl and M is selected from the group consisting of alkylene, alkenylene, arylene and alkarylene, and the parts R and M of the molecule independently of one another contain 0 to 12 carbon atoms and, in addition, may be substituted by a C.sub.1-3 alkoxy group. These compounds are made from polyisocyanates of formula A(NCO).sub.n and cyclic monoiminoethers containing hydroxyl groups and are suitable for subsequent processing to polymers.

Cyclic oligoiminoethers

Crosslinked polymers and process for their production

Liquid preparations for cleaning hard surfaces based on anionic surfactants either individually or in combination with nonionic surfactants or amphoteric surfactants, or nonionic surfactants either individually or in combination with cationic surfactants, solubilizers and, optionally, builders, dyes, perfumes and preservatives, containing an addition of polymers, namely cellulose ethers.

Liquid preparations for cleaning hard surfaces

N-substituted polyglycidyl urazole compounds of the general formula ##STR1## in which the radicals R represent a glycidyl radical corresponding to the following general formula ##STR2## wherein R.sub.1 represents hydrogen or an alkyl radical containing from 1 to 4 carbon atoms, or two of the radicals R represent a glycidyl radical of general formula II while the remaining radical R is a radical Z, other than said glycidyl radical, containing carbon, hydrogen and, optionally, heteroatoms, are useful in the treatment of various forms of leukemia.

N-substituted polyglycidyl urazole compounds, processes for their

Diglycidyl-substituted pteridine compounds of the general formula: ##STR1## wherein n is the whole number 1 or 2, R.sub.2 and R.sub.2 are the same or different, and are either hydrogen, a hydrocarbon radical, or together form a 5- or 6-membered carbocyclic or heterocyclic ring; processes for their preparation; and compositions and methods for their use as cytostatic agents.

Diglycidyl-pteridine compounds

New cytostatic compounds based on isocyanuric acid derivatives having 2 or 3 epoxide group containing substituents on ring nitrogen atoms, of which at least one differs from a glycidyl, having the formula ##STR1## wherein Oxiranyl is the same or different and has the formula ##STR2## wherein R.sub.1, R.sub.2 and R.sub.3 are the same or different and members selected from the group consisting of hydrogen, alkyl, haloalkyl, hydroxyalkyl and alkoxyalkyl and n in an integer from 1 to 8, with the proviso that if n is 1 in all oxiranyl groups, at least one of R.sub.1 or R.sub.3 is other than hydrogen, and R is a member selected from the group consisting of oxiranyl as defined above, hydrogen, alkyl, alkenyl, hydrocarbon aryl, hydrocarbon aralkyl, hydrocarbon alkaryl, cycloalkyl, and cycloalkenyl, optionally containing substituents. When R.sub.1, R.sub.2 and/or R.sub.3 denote alkyl or substituted alkyl in the oxiranyl radical, the alkyl radicals preferably have from 1 to 4 carbon atoms. The total number of carbon atoms in one oxiranyl radical should not be more than 10. The preparation of these compounds by introducing oxiranyl groups of Formula II and the radical R in known manner into the isocyanuric acid ring is also claimed.

Therapeutic compositions with a cytostatic action containing isocyanuric

Water-in-oil emulsions containing from 2 to 20% by weight of polymeric emulsifiers comprising statistical copolymers composed of units of the general formulae ##STR1## in the molar ratio of (I) to (II) of 2:1 to 20:1; wherein X is hydrogen or methyl, R.sub.1 is alkyl having 6 to 24 carbon atoms and R.sub.2 is ##STR2## 20 to 75% by weight of water; and the remainder to 100% by weight of conventional oily substances used in cosmetic emulsions.

Cosmetic emulsions containing copolymers of

Water-in-oil emulsions containing from 2 to 20% by weight of polymeric emulsifiers comprising statistical copolymers composed of units of the general formulae ##STR1## in the molar ratio of (I) to (II) of 2:1 to 20:1, wherein X is hydrogen or methyl, R.sub.1 is alkyl having 6 to 24 carbon atoms, and R.sub.2 is --CH.sub.2 --CH.sub.2 --OH, --CH.sub.2 --CH(OH)--CH.sub.3,--CH.sub.2 --CH(OH)--CH.sub.2 OH or --CH.sub.2 --CH.sub.2 --O--CH.sub.2 --CH.sub.2 --OH; 20 to 75% by weight of water; and the remainder to 100% by weight of conventional oily substances used in cosmetic emulsions.

Cosmetic emulsions containing copolymers of alkyl (meth) acrylates and

Water-in-oil emulsions containing from 2% to 20% by weight of polymeric emulsifiers comprising statistical copolymers composed of units of the general formulae ##STR1## in the molar ratio of (I) to (II) of 2:1 to 20:1, wherein X is hydrogen or methyl, R.sub.1 is alkyl having 6 to 24 carbon atoms, and R.sub.2 is --NH--CH.sub.2 OH, --NH--CH.sub.2 CH.sub.2 OH, or --N(CH.sub.2 CH.sub.2 OH).sub.2 ; 20 to 75% by weight of water; and the remainder to 100% by weight of conventional oily substances used in cosmetic emulsions.

Cosmetic emulsions containing copolymers of alkyl(meth)acrylates and

The method of activating aqueous solutions of percompounds utilizing N-acylated uracils and benzouracils as activators; solid activated compositions comprising solid percompounds and N-acylated uracils and benzouracils as activators; and novel diacylated uracils and benzouracils.

Growing community of inventors

Erkrath, Germany

Brigitte Hase