C07C211/14

PROCESS FOR MANUFACTURING ETHYLENEAMINE COMPOUNDS

Process for manufacturing ethyleneamine compounds selected from the group of ethyleneamines and hydroxyethylethyleneamines wherein the process comprises two reaction sequences.

PROCESS FOR MANUFACTURING ETHYLENEAMINE COMPOUNDS

Process for manufacturing ethyleneamine compounds selected from the group of ethyleneamines and hydroxyethylethyleneamines wherein the process comprises two reaction sequences.

Complexes and Ligands
20220025254 · 2022-01-27 ·

The present application provides ligands and fluorescent or luminescent complexes comprising these ligands.

Complexes and Ligands
20220025254 · 2022-01-27 ·

The present application provides ligands and fluorescent or luminescent complexes comprising these ligands.

Twin tail amine compounds and their zwitterionic derivatives

A compound of general formula (I) or (II), wherein R.sub.n and R.sub.m independently represent a C.sub.3-C.sub.27 aliphatic group, R.sub.1 to R.sub.4, which may be the same or different at each occurrence, represent hydrogen or a C.sub.1-C.sub.8 alkyl group, X.sub.1 and X.sub.2, which may be the same or different at each occurrence, represent a linear or branched divalent hydrocarbon radical with 1 to 24 carbon atoms which can be optionally substituted and/or interrupted by one or more heteroatoms or heteroatom containing groups, and R.sub.5 and R.sub.6, which may be the same or different at each occurrence, represent a group selected from —O.sup.−, -Alk-CH(OH)—CH.sub.2—SO.sub.3— and -Alk-CO.sub.2— wherein Alk represents an alkylene group. ##STR00001##

Twin tail amine compounds and their zwitterionic derivatives

A compound of general formula (I) or (II), wherein R.sub.n and R.sub.m independently represent a C.sub.3-C.sub.27 aliphatic group, R.sub.1 to R.sub.4, which may be the same or different at each occurrence, represent hydrogen or a C.sub.1-C.sub.8 alkyl group, X.sub.1 and X.sub.2, which may be the same or different at each occurrence, represent a linear or branched divalent hydrocarbon radical with 1 to 24 carbon atoms which can be optionally substituted and/or interrupted by one or more heteroatoms or heteroatom containing groups, and R.sub.5 and R.sub.6, which may be the same or different at each occurrence, represent a group selected from —O.sup.−, -Alk-CH(OH)—CH.sub.2—SO.sub.3— and -Alk-CO.sub.2— wherein Alk represents an alkylene group. ##STR00001##

TRIAMINE SOLIDIFICATION USING DIACIDS
20210352894 · 2021-11-18 ·

Stable, solid triamine compositions are disclosed. The pressed, cast, extruded or other solid compositions are suitable for antimicrobial, sanitizing and disinfectant applications. Ready-to-use solutions are obtained by dissolving the solid triamine compositions with water and the methods of use thereof are particularly suitable for cleaning, disinfecting, sanitizing, rinsing and/or lubricating. Beneficially, the solid triamine compositions are at least partially neutralized, allowing activity of 90% and greater of the biocidal triamine, and provide at least substantially similar or superior performance and micro efficacy to liquid formulations.

TRIAMINE SOLIDIFICATION USING DIACIDS
20210352894 · 2021-11-18 ·

Stable, solid triamine compositions are disclosed. The pressed, cast, extruded or other solid compositions are suitable for antimicrobial, sanitizing and disinfectant applications. Ready-to-use solutions are obtained by dissolving the solid triamine compositions with water and the methods of use thereof are particularly suitable for cleaning, disinfecting, sanitizing, rinsing and/or lubricating. Beneficially, the solid triamine compositions are at least partially neutralized, allowing activity of 90% and greater of the biocidal triamine, and provide at least substantially similar or superior performance and micro efficacy to liquid formulations.

TRIAMINE SOLIDIFICATION USING DIACIDS
20210352894 · 2021-11-18 ·

Stable, solid triamine compositions are disclosed. The pressed, cast, extruded or other solid compositions are suitable for antimicrobial, sanitizing and disinfectant applications. Ready-to-use solutions are obtained by dissolving the solid triamine compositions with water and the methods of use thereof are particularly suitable for cleaning, disinfecting, sanitizing, rinsing and/or lubricating. Beneficially, the solid triamine compositions are at least partially neutralized, allowing activity of 90% and greater of the biocidal triamine, and provide at least substantially similar or superior performance and micro efficacy to liquid formulations.

Process for making higher ethylene amines

Urea derivatives, methods for preparing ethylene amines, and methods of polymer manufacturing are provided. An exemplary method for preparing ethylene amines with n ethylene units and n+1 amine groups wherein n is at least 4, or urea derivatives of said ethylene amines, includes reacting an ethanolamine-functional compound, an amine-functional compound, and a carbon oxide delivering agent, wherein the ethanolamine-functional compound is of the formula HO—(C2H4-NH-)qH, q is at least 1, the amine-functional compound is of the formula H2N—(C2H4-NH-)rH, r is at least 1, the sum q+r is at least 4 and wherein optionally one or more of the ethanol-amine functional compound or amine-functional compound are at least partly used as their cyclic carbamate derivative, or linear or cyclic urea derivative.