Henkel Corporation

Amine salts, especially acetate salts prepared by neutralization of a fatty amine with acetic acid, are useflil as flotation agents (collectors), corrosion inhibitors, and lubricants (3,8). Amine acetates are commercially available from a number of suppHers Akzo Chemicals Inc. (Armac) (73) Henkel Corporation (formerly General Mills) (Alamac) (74) Jetco Chemicals Inc. (The Procter Gamble Company) (fet Amine) (75) Sherex (Adogen) (76) and Tom ah Products (Exxon Chemical Company) (Tomah) (77). 

Quantum Surfactants, Technical Bulletin 119, Henkel Corporation, Cincinnati, Ohio, May 1989. 

Lanolin alcohols are obtained by saponification of purified wool grease, a mixture of high molecular esters that is recovered in wool (qv) scouring. Ethoxylation of purified lanolin alcohols yields a full series of lipophilic and hydrophilic nonionic emulsifiers whose largest use is in cosmetic preparations. Manufacturers include Amerchol, Croda, ICI, Henkel Corporation, Westbrook Lanolin, Witco, and Pulcra, SA. 

Current address Coatings and Inks Division, Henkel Corporation, 300 Brookside Avenue,... 

Gruber B, Weese K, Mueller HP, Hill K, Behr A, Tucker J, Hoagland S (1992) W01991US0005214 Henkel Corporation Zucker Aktiengesellschaft Uelzen-Braunschweig Behr A, Urschey M (2003) J Mol Catal A 197 101-113... 

Azelaic Acid. This acid is produces by the Emery Group of Henkel Corporation in Cincinnati. Ohm. in mullimilfion kg quantities. The process that is currently used is based on (he o/onolysis of oleic acid (from grease or tallow followed by the decomposition of the ozunide with oxygen. 

Henkel Technologies Henkel Corporation Dial Corporation Dail International, Inc. 

There are commercially available fatty acids suitable for use in CLA production. For example, Henkel Corporation (106) sells a series of fat products including those shown in Table 2. However, none of the products listed in Table 2 would be preferred as starting materials for CLA production for reasons that will be discussed. 

A block copolymer of Henkel Corporation of Germany [(dodecyl oxide)-(ethylene oxide)3-(propylene oxide)g],... 

Henkel Corporation), and a co-surfactant for the carrier molecule (decyl alcohol, Sigma Chemical). The aqueous phase was slowly added to the oil phase under intense shear provided by a stator-type homo-genizer. All emulsions had similar internal droplet size and size distributions as analyzed by a Horiba CAPA 500 particle size... 

Guar and Derivatives Oilfield Applications Henkel Corporation Houston, TX, 1986. 

Materials. VEC was prepared by the catalyzed addition of CO2 to 3,4-epoxy-l-butene using conditions typical of that used industrially [77], then purified by vacuum distillation. Other raw materials were used as received without any additional purification. Mixed xylenes, vinyl acetate (VA), butyl acrylate (BA), butyl methacrylate (BMA), methyl methacrylate (MMA), styrene (St), and t-butyl hydroperoxide were obtained from Aldrich Chemical Company. Lupersol 575 (t-amyl peroxy (2-ethylhexanoate)) was supplied by Elf Atochem. Vazo 67 (2,2 -azobis(2-methylbutyronitrile)) was obtained from DuPont Chemical Company. Vinyl pivalate (NE05), vinyl 2-ethylhexanoate (V2EH), Tergitol NP-40 (non-ionic surfactant) and QP-300 (hydroxy ethyl cellulose) were obtained from Union Carbide Coq)oration. Aerosol OT-75 (surfactant) was obtained from Cytec. Sodium formaldehyde sulfoxylate was obtained from Henkel Corporation. Ethyl 3-ethoxy propionate (EEP), propylene glycol monomethyl ether (PM) and PM acetate (PM Ac) are Eastman Chemical Company products. 

Henkel Corporation, International Patent Application, PCT/US92/04962,1993. 

Henkel Corporation, Emery Group (use of tallow, preparation and testing of soaps, polymers, and lubricants) ... 

Rick Fay ter, senior research director at Henkel Corporation, Emery Group, notes, "Observing the Partners for Terrific Science program, I was heartened by the teachers spirit of innovation, enthusiasm, and dedication. 

S. M. Dershem, D. B. Patterson, and J. A. Osuna, Jr. Maleimide compounds in liquid form. US Patent 7102 015, assigned to Henkel Corporation (Rocky Hill, CT), September 5, 2006. 

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