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:
May. 04, 2021

Filed:

Nov. 13, 2019
Applicant:

Inolex Investment Corporation, Wilmington, DE (US);

Inventors:

Rocco V. Burgo, Mullica Hill, NJ (US);

Michael E. Wright, Hurricane, UT (US);

Gary B. Mosser, Tabernacle, NJ (US);

Michael J. Fevola, Belle Mead, NJ (US);

Assignee:

INOLEX INVESTMENT CORPORATION, Wilmington, DE (US);

Attorney:
Primary Examiner:
Int. Cl.
CPC ...
C07C 29/04 (2006.01); C07C 31/20 (2006.01); C07C 29/80 (2006.01); B01J 23/06 (2006.01); B01J 37/08 (2006.01); B01J 21/04 (2006.01); C11D 3/20 (2006.01); C07C 1/24 (2006.01); C07C 29/48 (2006.01); C07C 11/02 (2006.01); C07C 11/107 (2006.01); C07B 41/02 (2006.01); C07B 63/00 (2006.01); A61L 2/18 (2006.01); A01N 31/02 (2006.01); A61K 8/34 (2006.01); A61Q 5/00 (2006.01); A61Q 11/00 (2006.01); A61Q 19/00 (2006.01); C11D 3/48 (2006.01);
U.S. Cl.
CPC ...
C07C 29/04 (2013.01); B01J 21/04 (2013.01); B01J 23/06 (2013.01); B01J 37/08 (2013.01); C07C 1/24 (2013.01); C07C 11/02 (2013.01); C07C 11/107 (2013.01); C07C 29/48 (2013.01); C07C 29/80 (2013.01); C07C 31/20 (2013.01); C11D 3/2044 (2013.01); A01N 31/02 (2013.01); A61K 8/345 (2013.01); A61L 2/18 (2013.01); A61Q 5/00 (2013.01); A61Q 11/00 (2013.01); A61Q 19/00 (2013.01); B01J 2523/27 (2013.01); B01J 2523/31 (2013.01); C07B 41/02 (2013.01); C07B 63/00 (2013.01); C07C 2521/04 (2013.01); C11D 3/48 (2013.01);
Abstract

A process is incorporated herein for the synthesis of bio-1,2-alkanediols, comprising: providing a bio-alkene having a carbon chain of about 5 to about 20 carbon atoms and a bio-1-alkene regioselectivity of at least about 80%, at least about 92% and/or at least about 95%; and converting the bio-alkene to a bio-1,2-alkanediol having a carbon chain length of about 5 to about 20 carbon atoms. Methods for treating catalysts which may be incorporated in the process for the synthesis of bio-1,2-alkanediols are also included herein. Such bio-1,2-alkanediols are used in compositions and products alone as antimicrobial materials, or with existing bio-compounds and/or antimicrobials, preservatives, alternative preservation systems and/or hurdle technology components. The bio-1,2-alkanediols incorporate a natural and bio-based pathway for antimicrobial effects in various compositions such as cosmetic, pharmaceutical, industrial and household products.


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