Abstract: Process for the manufacture of diglycidylesters of &agr;,&agr;′-branched dicarboxylic acids, comprising (a) the reaction of the &agr;,&agr;′-branched dicarboxylic acid with a halo substituted monoepoxide such as an epihalohydrin, in a 1.1-20 acid equivalent ratio relative to the &agr;,&agr;′-branched aliphatic dicarboxylic acid, optionally in the presence of water and water-miscible solvent, and in the presence of a catalyst in an amount of at most 45 mol % of the acid equivalent amount of the &agr;,&agr;′-branched aliphatic dicarboxylic acid, at a temperature in the range of from 30 to 110° C., during a period in the range of from 0.5 to 2.5 hr, (b) addition of alkali metal hydroxide or alkali metal alkanolate up to an acid equivalent ratio as to the &agr;,&agr;′-branched aliphatic dicarboxylic acid in the range of from 0.9:1 to 1.2:1, and reaction at a temperature of from 0 to 80° C.

Abstract: Carboxyl functional polyester resins obtainable by reaction of: a) at least a compound of the formula  wherein a≧1, and wherein R1 and R2 each may represent an alkyl group having from 1 to 4 carbon atoms or wherein R1 and R2 may form together with the group —CH—(CH2)x—CH˜ a cycloalkyl group and preferably 1,4-cyclohexane dicarboxylic acid (A1), mixed with smaller molar amounts of monoglycidyl esters of &agr;,&agr;-branched carboxyl acids containing from 5 to 19 carbon atoms in the acid moiety (A2), and b) at least one compound B comprising one primary- or secondary hydroxyl group and one tertiary aliphatic carboxyl group, and c) optionally one diol compound C, and d) optionally a dihydroxymonocarboxylic acid compound D, and e) optionally a trihydroxyalkane (E1) or tetrahydroxyalkane (E2), the molar ratio of compounds A1:(C+A2):B:D:E1:E2, being, (X+Y+1):Y:2:X:Q:P, wherein X ranges from 0 to 8, Y ranges from 1 to 8, Q ranges from 0 to 3 and w

Abstract: Linear, tertiary carboxyl functional polyester resins are obtained by reaction of (a) at least one 1,4-dicarboxylcyclohexane (A), optionally mixed with a minor weight fraction of an alkane dicarboxylic acid containing in the range of from 8 to 16 carbons atoms (A′), (b) at least one dihydroxymonocarboxylic acid compound (B) containing a tertiary aliphatic carboxyl group and two aliphatic hydroxyl groups, (c) optionally, one diol compound (C) containing two aliphatic hydroxyl groups, each independently being a primary or a secondary hydroxyl group, and (d) optionally, a compound (D′) containing one monofunctional primary or secondary hydroxyl group and/or a compound (D″) containing one primary or secondary hydroxyl group and one tertiary aliphatic carboxyl group, the molar ratio of the compounds (A+A′):B:C:D′:D″ being X+Y+1:Y:X:M:N wherein M+N is in the range of from 0 to 2, wherein X ranges from 2 to 8, and Y ranges from [2−(M+N)&rsq