IP Library Granted Patent US 8,399,389
Granted Patent B2
US 8,399,389 · App. 13/587,120 · Granted Mar 19, 2013

Food-grade lubricant compositions comprising estolide compounds

Inventors: Jakob Bredsguard (Irvine, CA); Jeremy Forest (Tustin, CA); Travis Thompson (Anaheim, CA)
Assignee: Biosynthetic Technologies, LLC
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 8,399,389
App. No.
13/587,120
Granted
Mar 19, 2013
Kind
B2
Abstract

Provided herein are compositions comprising at least one estolide compound of formula: in which n is an integer equal to or greater than 0; m is an integer equal to or greater than 1; R 1 , independently for each occurrence, is selected from optionally substituted alkyl that is saturated or unsaturated, and branched or unbranched; R 2 is selected from hydrogen and optionally substituted alkyl that is saturated or unsaturated, and branched or unbranched; and R 3 and R 4 , independently for each occurrence, are selected from optionally substituted alkyl that is saturated or unsaturated, and branched or unbranched. Also provided are uses of the compositions described herein.

Claims (37)

1. A method of lubricating food service equipment, comprising contacting at least a portion of the food service equipment with a food-grade lubricant composition comprising at least one estolide compound selected from compounds of Formula I:

wherein

x is, independently for each occurrence, an integer selected from 0 to 20;

y is, independently for each occurrence, an integer selected from 0 to 20;

n is an integer greater than or equal to 0;

R 1 is an optionally substituted alkyl that is saturated or unsaturated, and branched or unbranched; and

R 2 is an optionally substituted alkyl that is saturated or unsaturated, and branched or unbranched,

wherein each fatty acid chain residue of said at least one estolide compound is independently optionally substituted.

2. The method according to claim 1 , wherein

x is, independently for each occurrence, an integer selected from 1 to 10;

y is, independently for each occurrence, an integer selected from 1 to 10;

n is an integer selected from 0 to 8;

R 1 is an optionally substituted C 1 to C 22 alkyl that is saturated or unsaturated, and branched or unbranched; and

R 2 is an optionally substituted C 1 to C 22 alkyl that is saturated or unsaturated, and branched or unbranched,

wherein each fatty acid chain residue is unsubstituted.

3. The method according to claim 2 , wherein

x+y is, independently for each chain, an integer selected from 13 to 15; and

n is an integer selected from 0 to 6.

4. The method according to claim 3 , wherein x is, independently for each occurrence, an integer selected from 7 and 8.

5. The method according to claim 3 , wherein y is, independently for each occurrence, an integer selected from 7 and 8.

6. The method according to claim 1 , wherein R 2 is an unsubstituted alkyl that is saturated or unsaturated, and branched or unbranched.

7. The method according to claim 6 , wherein R 2 is an unsubstituted C 1 to C 20 alkyl that is saturated or unsaturated and branched or unbranched.

8. The method according to claim 7 , wherein R 2 is selected from methyl, ethyl, propyl, butyl, pentyl, hexyl, heptyl, octyl, nonyl, decanyl, undecanyl, dodecanyl, tridecanyl, tetradecanyl, pentadecanyl, hexadecanyl, heptadecanyl, octadecanyl, nonadecanyl, and icosanyl, which are saturated or unsaturated and branched or unbranched.

9. The method according to claim 7 , wherein R 2 is an unsubstituted C 6 to C 12 alkyl that is saturated and branched.

10. The method according to claim 1 , wherein R 1 is an unsubstituted alkyl that is saturated or unsaturated, and branched or unbranched.

11. The method according to claim 10 , wherein R 1 is an unsubstituted C 1 to C 20 alkyl that is saturated or unsaturated, and branched or unbranched.

12. The method according to claim 11 , wherein R 1 is selected from methyl, ethyl, propyl, butyl, pentyl, hexyl, heptyl, octyl, nonyl, decanyl, undecanyl, dodecanyl, tridecanyl, tetradecanyl, pentadecanyl, hexadecanyl, heptadecanyl, octadecanyl, nonadecanyl, and icosanyl, which are saturated or unsaturated and branched or unbranched.

13. The method according to claim 11 , wherein R 1 is an unsubstituted C 7 to C 17 alkyl that is unbranched and saturated or unsaturated.

14. The method according to claim 13 , wherein R 1 is saturated.

15. The method according to claim 1 , wherein said food-grade lubricant composition has an EN selected from an integer or fraction of an integer that is equal to or less than 2, wherein EN is the average number of estolide linkages in compounds according to Formula I.

16. The method according to claim 15 , wherein said at least one estolide compound has a kinematic viscosity equal to or less than 55 cSt when measured at 40° C.

17. The method according to claim 16 , wherein said at least one estolide compound has a pour point equal to or lower than −25° C.

18. The method according to claim 1 , wherein said food-grade lubricant composition further comprises at least one polyalphaolefin.

19. The method according to claim 18 , wherein the at least one polyaphaolefin is selected from one or more of PAO2, PAO4, PAO6, PAO8, PAO9, PAO10, PAO40, or PAO100.

20. The method according to claim 1 , wherein said food-grade lubricant composition further comprises at least one antioxidant.

21. The method according to claim 20 , wherein the at least antioxidant is selected from one or more of an amine antioxidant, a phenolic antioxidant, or an organometallic antioxidant.

22. The method according to claim 1 , wherein said food-grade lubricant composition further comprises at least one of a separation preventer, a stability enhancer, a surfactant, a biocide, a corrosion inhibitor, an abrasion inhibitor, a viscosity index improver, a pour point depressant, a dispersant, or an antifoaming agent.

Assignments (8)
ASSIGNMENT OF SECURITY INTEREST Recorded Mar 23, 2018
From: BP TECHNOLOGY VENTURES INC.
To: BIOSYN HOLDINGS, LLC
Reel/Frame 045688/0600 →
ASSIGNMENT OF SECURITY INTEREST Recorded Mar 23, 2018
From: EVONIK CORPORATION
To: BIOSYN HOLDINGS, LLC
Reel/Frame 045860/0547 →
ASSIGNMENT OF SECURITY INTEREST Recorded Mar 23, 2018
From: EVONIK OIL ADDITIVES USA, INC.
To: BIOSYN HOLDINGS, LLC
Reel/Frame 045684/0293 →
RELEASE OF SECURITY INTEREST Recorded Feb 13, 2018
From: SILICON VALLEY BANK
To: BIOSYNTHETIC TECHNOLOGIES, LLC
Reel/Frame 044916/0936 →
SECURITY INTEREST Recorded Jan 30, 2018
From: BIOSYNTHETIC TECHNOLOGIES, LLC
To: BP TECHNOLOGY VENTURES INC.
Reel/Frame 045196/0587 →
SECURITY INTEREST Recorded Mar 18, 2016
From: BIOSYNTHETIC TECHNOLOGIES, LLC
To: EVONIK OIL ADDITIVES USA, INC.
Reel/Frame 038146/0859 →
SECURITY INTEREST Recorded Nov 30, 2015
From: BIOSYNTHETIC TECHNOLOGIES, LLC
To: EVONIK CORPORATION
Reel/Frame 037162/0364 →
SECURITY INTEREST Recorded Dec 20, 2014
From: BIOSYNTHETIC TECHNOLOGIES, LLC
To: SILICON VALLEY BANK
Reel/Frame 034562/0322 →
Continuity (5)
Continuation 13531923 · Jun 25, 2012
Continuation 13404903 · Feb 24, 2012
Provisional Application 61498499 · Jun 17, 2011
Provisional Application 61569046 · Dec 9, 2011
Related Publication 20130023454A1 · Jan 24, 2013