Abstract: The use of hexahydrophthalimide compounds of the formula (I) is described as plasticizers for molding compositions, in particular polyvinyl chloride, in which R is alkyl, cycloalkyl, or cycloalkylalkyl, where the two last named moieties can be unsubstituted or alkyl-substituted, and the moiety R has at least 6 carbon atoms.

Abstract: Selected cyclohexane-1,3- and -1,4-dicarboxylic acid esters are described, as is their use as plasticizers in plastics and their preparation by hydrogenation of the corresponding isophthalic or terephthalic esters by bringing one or more of these isophthalic or terephthalic esters into contact with a hydrogen-containing gas in the presence of a catalyst which comprises, as active metal, at least one metal of the 8th transition group of the Periodic Table on its own or together with at least one metal of the 1st or 7th transition group of the Periodic Table, applied to a support, which comprises using a support having micropores.

Abstract: A process for producing plasticizers in which a phthalic acid having the CAS Nos. 111381-89-6, 111381-90-9, 111381-91-0, 68515-44-6, 68515-45-7 and 3648-20-7, the formed plasticizers and a method of increasing the plasticity of a plastic product.

Abstract: Polysiloxane sols preparable by subjecting (1) in a first stage (A) a silicon compound of the general formula I: (ZoL-)mSi(H)n(R)p??(I), which is free of carbamate groups and where o is an integer from 1 to 5; m is 0, 1, 2 or 3; n is an integer from 1 to 4; p is 0, 1 , 2 or 3; Z is a reactive functional group, excluding carbamate group; L is an at least divalent, linking, organic group; H is a hydrolyzable, monovalent, organic group or hydrolyzable atom; R is a nonhydrolyzable, monovalent, organic group; to partial hydrolysis and condensation in the presence (B) of at least one crosslinking agent, and then subjecting (2) in a further stage, the reaction mixture (1) to complete hydrolysis and condensation with (C) a hydrolyzable, carbamate-functional silicon compound of the general formula II: {[HR1N—(O)C—O—]rL-}sSi(H)t(R)u??(II) where R1 is a hydrogen atom or group R; r is an integer from 1 to 5; s is 1, 2 or 3; t is 1, 2 or 3; u 0, 1 or 2; and their use as coating materials, adhesives, and sealing c

Abstract: The present invention relates to a process for the preparation of aliphatic, cycloaliphatic, araliphatic and aromatic mono- and oligoisocyanates by phosgenation of the corresponding primary amines at atmospheric pressure, which comprises a) introducing a catalytic amount of a monoisocyanate (isocyanate a) into an inert solvent together with phosgene; b) adding the primary amine, and c) reacting the resulting reaction mixture with phosgene.

Abstract: The mixture described is a mixture of isomeric nonanol diesters of a dicarboxylic acid, selected from the class consisting of a mixture of diesters of adipic acid in the 1H NMR spectrum of which, observed in CDCl3, the ratio of the area under the resonance signals at chemical shifts in the range from 1.0 to 2.0 ppm with respect to TMS to the area under the resonance signals at chemical shifts in the range from 0.5 to 1.0 ppm with respect to TMS is from 1.20 to 5.00 and a mixture of diesters of phthalic acid, in the 1H NMR spectrum of which, observed in CDCl3, the ratio of the area under the resonance signals at chemical shifts in the range from 1.1 to 3.0 ppm with respect to TMS to the area under the resonance signals at chemical shifts in the range from 0.5 to 1.1 ppm with respect to TMS is from 1.00 to 4.00.

Abstract: A process for hydrogenating benzenepolycarboxylic acids or a derivatives thereof by bringing one or more benzenepolycarboxylic acids or derivatives thereof into contact with a hydrogen-containing gas is carried out in the presence of a catalyst containing macropores. The catalyst contains, as an active metal, at least one metal of transition group VIII of the Periodic Table alone or together with at least one metal of transition group I or VII of the Periodic Table. Except that hydrogenation of dimethyl terephthalate using a catalyst containing ruthenium as active metal, either alone or together with at least one metal of transition group I, VII or VIII of the Periodic Table, applied to a support having a mean pore diameter of at least 50 nm and a BET surface are of at most 30 m2/g, where the active metal is present in an amount of from 0.01 to 30% by weight, based on the total weight of the catalyst, and the ratio of the surface areas of the active metal and the catalyst support is less than 0.

Abstract: A process for hydrogenating a benzenepolycarboxylic acid or a derivative thereof or a mixture of two or more thereof by bringing the benzenepolycarboxylic acid or the derivative thereof or the mixture of two or more thereof into contact with a hydrogen-containing gas is carried out in the presence of a catalyst which comprises as active metal at least one metal of transition group VIII of the Periodic Table alone or together with at least one metal of transition group I or VII of the periodic table applied to a support which contains macropores with the proviso that if dimethyl terephthalate is hydrogenated, the hydrogenation using a catalyst which comprises as active metal ruthenium either alone or together with at least one metal of transition group I, VII or VIII of the Periodic Table applied to a support, where the support has a mean pore diameter of at least 50 nm and a BET surface area of at most 30 m2/g and the amount of the active metal is from 0.

Abstract: Monoacetals of aromatic 1,2-diketones are manufactured by reacting the corresponding 1,2-diketones, in an organic solvent, with an acid ester (R.sup.1).sub.n X as alkylating agent and an alcoholate (R.sup.2 O).sub.m Me, where R.sup.1 and R.sup.2 are identical or different hydrocarbon radicals of 1 to 12 carbon atoms, which may or may not be substituted, n and m are integers from 1 to 3, X is a monobasic, dibasic or tribasic acid radical and Me is a metal of main groups 1 to 3 of the periodic table of the elements. The resulting diketone monoacetals are particularly suitable for use as photoinitiators in photopolymerizable compositions.

Abstract: Aminosulfonylcarboxylic acids and their manufacture from diamines and chlorosulfonylcarboxylic acids.

Abstract: Aminosulfonylcarboxylic acids and their manufacture from diamines and chlorosulfonylcarboxylic acids.