Patent classifications
C07C211/63
SUPER-COOLING RELEASE MATERIAL AND METHOD FOR PRODUCING SAME
A supercooling release material, which releases a supercooled state of a cold storage material including one or more types of alkylammonium halide aqueous solutions that generate a hydrate by being cooled to a hydrate generation temperature or lower, includes: an alkylammonium ion included in the cold storage material; and a metal halide ion which has, as a constituent element, a halogen element included in the cold storage material. The supercooled state of the cold storage material can be reliably released by using the supercooling release material having such a configuration.
SUPER-COOLING RELEASE MATERIAL AND METHOD FOR PRODUCING SAME
A supercooling release material, which releases a supercooled state of a cold storage material including one or more types of alkylammonium halide aqueous solutions that generate a hydrate by being cooled to a hydrate generation temperature or lower, includes: an alkylammonium ion included in the cold storage material; and a metal halide ion which has, as a constituent element, a halogen element included in the cold storage material. The supercooled state of the cold storage material can be reliably released by using the supercooling release material having such a configuration.
SYNTHESIS OF MOLECULAR SIEVE SSZ-63
A method is disclosed for synthesizing molecular sieve SSZ-63 using 1-(decahydronaphthalen-2-yl)-1-methylpyrrolidinium cations as a structure directing agent.
Fatty amines, amidoamines, and their derivatives from natural oil metathesis
Fatty amine compositions made from a metathesis-derived C10-C17 monounsaturated acid, octadecene-1,18-dioic acid, or their ester derivatives are disclosed. In another aspect, fatty amidoamines made by reacting a metathesis-derived C10-C17 monounsaturated acid, octadecene-1,18-dioic acid, or their ester derivatives with an aminoalkyl-substituted tertiary amine are disclosed. The fatty amines or amidoamines are advantageously sulfonated, sulfitated, oxidized, or reduced. In other aspects, the ester derivative is a modified triglyceride made by self-metathesis of a natural oil or an unsaturated triglyceride made by cross-metathesis of a natural oil with an olefin.
Fatty amines, amidoamines, and their derivatives from natural oil metathesis
Fatty amine compositions made from a metathesis-derived C10-C17 monounsaturated acid, octadecene-1,18-dioic acid, or their ester derivatives are disclosed. In another aspect, fatty amidoamines made by reacting a metathesis-derived C10-C17 monounsaturated acid, octadecene-1,18-dioic acid, or their ester derivatives with an aminoalkyl-substituted tertiary amine are disclosed. The fatty amines or amidoamines are advantageously sulfonated, sulfitated, oxidized, or reduced. In other aspects, the ester derivative is a modified triglyceride made by self-metathesis of a natural oil or an unsaturated triglyceride made by cross-metathesis of a natural oil with an olefin.
CATIONIC CARBOHYDRATE POLYMERS FOR FABRIC CARE
A fabric care composition comprising a modified carbohydrate polymer having quaternary ammonium groups having at least one C.sub.8-C.sub.22 alkyl or alkenyl group. The modified carbohydrate polymer has a weight-average molecular weight of at least 500,000.
CATIONIC CARBOHYDRATE POLYMERS FOR FABRIC CARE
A fabric care composition comprising a modified carbohydrate polymer having quaternary ammonium groups having at least one C.sub.8-C.sub.22 alkyl or alkenyl group. The modified carbohydrate polymer has a weight-average molecular weight of at least 500,000.
METHOD FOR PREPARING AMINES FROM CARBONYL COMPOUNDS BY TRANSAMINASE REACTION UNDER SALT PRECIPITATION
Described herein is a method for preparing an amino salt compound, the method including: i) providing a carbonyl compound; ii) reacting the carbonyl compound provided according to (i) in the presence of a transaminase with ii-a) at least one primary amine; and ii-b) at least one carboxylic acid; thereby obtaining a mixture including an at least partially crystallized amino salt compound including a cation and a carboxylate anion based on the at least one carboxylic acid added according to (ii-b). Also described herein is an amino salt compound obtained or obtainable by the method and to the amino salt compound, and a composition including a) an amine of general formula (IIa); and b) at least one carboxylic acid of general formula (III).
METHOD FOR PREPARING AMINES FROM CARBONYL COMPOUNDS BY TRANSAMINASE REACTION UNDER SALT PRECIPITATION
Described herein is a method for preparing an amino salt compound, the method including: i) providing a carbonyl compound; ii) reacting the carbonyl compound provided according to (i) in the presence of a transaminase with ii-a) at least one primary amine; and ii-b) at least one carboxylic acid; thereby obtaining a mixture including an at least partially crystallized amino salt compound including a cation and a carboxylate anion based on the at least one carboxylic acid added according to (ii-b). Also described herein is an amino salt compound obtained or obtainable by the method and to the amino salt compound, and a composition including a) an amine of general formula (IIa); and b) at least one carboxylic acid of general formula (III).
CARBONIC ACID ADDUCTS
The present invention relates to a carbonic acid adduct (CAA) comprising carbonic acid, at least one amine, and optionally at least one salt, said adduct being producible by a method comprising the following steps: a) providing a solution (A) comprising dissolved CO.sub.2; optionally b) dissolving a base (BA) not corresponding to the amine (AM) in the solution (A) so as to obtain the solution (A1); c) dissolving the at least one amine (AM) in the solution (A) or (A1) so as to obtain the solution (B); d) freezing the solution obtained after completion of step c); and e) storing the solution frozen in step d) at −100 to 0° C. for no longer than 4 days. The content of CO.sub.2 in the solution that is subjected to step c) is at least 6 g/l. The invention also relates to a method for producing the carbonic acid adduct (CAA), a pharmaceutical preparation (PP) comprising the carbonic acid adduct (CAA), and methods for the production thereof and use of the carbonic acid adduct (CAA) or the pharmaceutical preparation (PP) in therapy for a range of indications.