The patent badge is an abbreviated version of the USPTO patent document. The patent badge does contain a link to the full patent document.

The patent badge is an abbreviated version of the USPTO patent document. The patent badge covers the following: Patent number, Date patent was issued, Date patent was filed, Title of the patent, Applicant, Inventor, Assignee, Attorney firm, Primary examiner, Assistant examiner, CPCs, and Abstract. The patent badge does contain a link to the full patent document (in Adobe Acrobat format, aka pdf). To download or print any patent click here.

Date of Patent:
Feb. 21, 2017

Filed:

Sep. 08, 2015
Applicant:

Stepan Company, Northfield, IL (US);

Inventors:

Dave R Allen, Chicago, IL (US);

Marcos Alonso, Chicago, IL (US);

Randal J Bernhardt, Antioch, IL (US);

Aaron Brown, Chicago, IL (US);

Kelly Buchek, Hoffman Estates, IL (US);

Sangeeta Ganguly-Mink, Chicago, IL (US);

Brian Holland, Deerfield, IL (US);

Gary Luebke, Chicago, IL (US);

Renee Luka, Park Ridge, IL (US);

Andrew D. Malec, Irvine, CA (US);

Ronald A Masters, Glenview, IL (US);

Dennis S Murphy, Libertyville, IL (US);

Irene Shapiro, Buffalo Grove, IL (US);

Patti Skelton, Winder, GA (US);

Brian Sook, Lawrenceville, GA (US);

Michael R Terry, Gurnee, IL (US);

Gregory Wallace, Chicago, IL (US);

Laura Lee Whitlock, Highland Park, IL (US);

Michael Wiester, Chicago, IL (US);

Patrick Shane Wolfe, Palatine, IL (US);

Lena Titievsky, Chicago, IL (US);

Assignee:

Stepan Company, Northfield, IL (US);

Attorney:
Primary Examiner:
Int. Cl.
CPC ...
C11D 3/32 (2006.01); C07C 233/09 (2006.01); A01N 25/02 (2006.01); A01N 25/04 (2006.01); A01N 25/30 (2006.01); A01N 33/12 (2006.01); A01N 37/18 (2006.01); A01N 37/44 (2006.01); A01N 41/04 (2006.01); A61K 8/41 (2006.01); A61K 8/42 (2006.01); A61K 8/44 (2006.01); A61K 8/46 (2006.01); A61K 8/92 (2006.01); A61Q 5/12 (2006.01); A61Q 19/10 (2006.01); A62D 1/02 (2006.01); B01F 17/00 (2006.01); C07C 69/533 (2006.01); C07C 69/593 (2006.01); C07C 209/12 (2006.01); C07C 211/21 (2006.01); C07C 219/08 (2006.01); C07C 231/12 (2006.01); C07C 237/16 (2006.01); C07C 303/18 (2006.01); C08G 65/26 (2006.01); C08K 5/01 (2006.01); C08K 5/20 (2006.01); C09K 8/00 (2006.01); C09K 15/28 (2006.01); C11C 3/00 (2006.01); C11C 3/08 (2006.01); C11D 1/00 (2006.01); C11D 1/04 (2006.01); C11D 1/28 (2006.01); C11D 1/62 (2006.01); C11D 1/65 (2006.01); C11D 1/74 (2006.01); C11D 1/83 (2006.01); C11D 1/90 (2006.01); C11D 1/92 (2006.01); C11D 1/94 (2006.01); C11D 3/48 (2006.01); A61Q 5/02 (2006.01); C07C 233/20 (2006.01); C07C 233/38 (2006.01); C07C 309/15 (2006.01); C07D 233/24 (2006.01); C09D 7/02 (2006.01); C09K 8/54 (2006.01); C11D 1/66 (2006.01);
U.S. Cl.
CPC ...
C07C 233/09 (2013.01); A01N 25/02 (2013.01); A01N 25/04 (2013.01); A01N 25/30 (2013.01); A01N 33/12 (2013.01); A01N 37/18 (2013.01); A01N 37/44 (2013.01); A01N 41/04 (2013.01); A61K 8/416 (2013.01); A61K 8/42 (2013.01); A61K 8/44 (2013.01); A61K 8/466 (2013.01); A61K 8/92 (2013.01); A61Q 5/02 (2013.01); A61Q 5/12 (2013.01); A61Q 19/10 (2013.01); A62D 1/0071 (2013.01); B01F 17/0028 (2013.01); B01F 17/0057 (2013.01); C07C 69/533 (2013.01); C07C 69/593 (2013.01); C07C 209/12 (2013.01); C07C 211/21 (2013.01); C07C 219/08 (2013.01); C07C 231/12 (2013.01); C07C 233/20 (2013.01); C07C 233/38 (2013.01); C07C 237/16 (2013.01); C07C 303/18 (2013.01); C07C 309/15 (2013.01); C07D 233/24 (2013.01); C08G 65/2615 (2013.01); C08K 5/01 (2013.01); C08K 5/20 (2013.01); C09D 7/02 (2013.01); C09K 8/00 (2013.01); C09K 8/54 (2013.01); C09K 15/28 (2013.01); C11C 3/00 (2013.01); C11C 3/08 (2013.01); C11D 1/002 (2013.01); C11D 1/04 (2013.01); C11D 1/28 (2013.01); C11D 1/62 (2013.01); C11D 1/652 (2013.01); C11D 1/66 (2013.01); C11D 1/74 (2013.01); C11D 1/83 (2013.01); C11D 1/90 (2013.01); C11D 1/92 (2013.01); C11D 1/94 (2013.01); C11D 3/48 (2013.01);
Abstract

Fatty amide compositions and their derivatives are disclosed. The fatty amides comprise a reaction product of a metathesis-derived C-Cmonounsaturated acid, octadecene-1,18-dioic acid, or their ester derivatives with a primary or secondary amine. Derivatives made by reducing, quaternizing, sulfonating, alkoxylating, sulfating, and sulfitating the fatty amide are also included. The amine reactant can be diethylenetriamine or (2-aminoethyl)ethanolamine, which provide imidazoline amides or esters, respectively. In one aspect, the ester derivative of the C-Cmonounsaturated acid or octadecene-1,18-dioic acid is a lower alkyl ester. 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. The compositions are valuable for cleaners, fabric treatment, hair conditioning, personal care, antimicrobial compositions, agricultural uses, and oil field applications.


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