Abstract: A cleaning formulation is formulated from an ethoxylated alcohol or nonionic at 15-50%, an ethoxylated amine at 10-50%, an anionic at 5-50%, a non-water soluble solvent at 0.5-15%, a water and organic soluble solvent at 1-25%, an optional acrylate based polymer, optional dyes and perfumes, and the remainder water.

Abstract: A cleaning formulation is formulated from an ethoxylated alcohol or nonionic at 15-50%, an ethoxylated amine at 10-50%, an anionic at 5-50%, a non-water soluble solvent at 0.5-15%, a water and organic soluble solvent at 1-25%, an optional acrylate based polymer, optional dyes and perfumes, and the remainder water.

Abstract: The present invention relates to quaternary ammonium compounds and formulations thereof useful as cleaning compositions, antistatic compounds, fabric softeners, hair conditioners, skin conditioners, paper deinking and ink floatation, agents, and the like.

Abstract: A composition comprising: (a) a compound of the following structural formula: wherein each of R* and R** is independently a linear, branched or cyclic alkylene group containing 2 to 12 carbon atoms, wherein no two nitrogen atoms are separated by fewer than 2 carbon atoms; each of A1, A2, A3, A4, and A5 is independently a straight or branched alkylene containing 2 to 4 carbon atoms; each of R1, R2, R3, R4, and R5 is independently —H or RAC(O)— wherein RA is straight or branched alkyl or alkenyl containing 7 to 21 carbon atoms and 0 to 4 carbon-carbon double bonds; provided that at least one of R1, R2, R3, R4, or R5 is RAC(O)—; each of Q1, Q2 and Q3 is independently —H, —CH3, —C2H5, —C3H7, —C4H5, benzyl, —CH2COOH, or —CH2COOA−; or, if R* is a —CH2CH2— group, Q1 and Q3 together or Q1 and Q2 together may be a —CH2CH2— group to form a six-membered piperazine ring; or, if R** is a —CH2CH2— group,

Abstract: The present invention is directed to polyamines represented by the following general structure: ##STR1## where R is an organic group, R' is H or CH.sub.3, andx=0-3Tri, tetra, penta, and hexa amines, accordingly, are disclosed.The method for making the novel polyamines comprises a multi-step reaction that commences in step (a) with the cyanoethylation of a primary amine, R--NH.sub.2, with acrylonitrile under cyanoethylation conditions to form an aminonitrile of the structure R--NH--CH.sub.2 --CH.sub.2 --CN. The aminonitrile in step (b) is methylated by reaction with formic acid and formaldehyde under Leuckart reaction conditions to form a monomethyl aminonitrile of the structure R--N(CH.sub.3)--CH.sub.2 --CH.sub.2 --CN. The monomethyl aminonitrile then in step (c) is reduced, preferably by hydrogenation under hydrogenation conditions, to form a monomethyl diamine of the structure R--N(CH.sub.3)--CH.sub.2 --CH.sub.2 --CH.sub.2 --NH.sub.2.