IP Library Granted Patent US 11,767,278
Granted Patent B2
US 11,767,278 · App. 17/340,952 · Granted Sep 26, 2023

Plant extract compositions for forming protective coatings

Inventors: Ronald C. Bakus, II (Santa Barbara, CA); Louis Perez (Santa Barbara, CA); Camille Mol (Santa Barbara, CA); James Rogers (Santa Barbara, CA); Gabriel Rodriguez (Goleta, CA)
Assignee: Apeel Technology, Inc.
C07C29/132B01D11/0288C07C29/17C07C51/00C07C51/09C07C51/36C07C51/367C07C51/377C07C63/00C07C67/03C07C67/08C07C67/475C07D303/38C08G63/06C08J11/14C08J11/24A23B7/16A23L3/3454A23V2002/00B01D11/0284C08G63/00C08J2391/06C09D5/00C09D167/00C09D167/04
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Quick Facts
Patent No.
US 11,767,278
App. No.
17/340,952
Granted
Sep 26, 2023
Kind
B2
Abstract

Described herein are methods of preparing cutin-derived monomers, oligomers, or combinations thereof from cutin-containing plant matter. The methods can include heating the cutin-derived plant matter in a solvent at elevated temperature and pressure. In some preferred embodiments, the methods can be carried out without the use of additional acidic or basic species.

Claims (35)

1. A method of preparing a composition comprising monomers, oligomers, or both derived from cutin, the method comprising:

combining cutin-containing plant matter with a solvent to yield a mixture, wherein the solvent comprises a nucleophilic solvent, and has a boiling point at a first temperature at a first pressure of one atmosphere; and

increasing the temperature of the mixture to a second temperature and the pressure of the mixture to a second pressure to yield a composition comprising monomers, oligomers, or both derived from cutin, wherein the second temperature is greater than the first temperature and the second pressure is greater than one atmosphere, and wherein the monomers, oligomers, or both comprise esters.

2. The method of claim 1 , wherein the solvent comprises ethanol and the monomers, oligomers, or both comprise ethyl esters.

3. The method of claim 1 , wherein the solvent comprises methanol and the monomers, oligomers, or both comprise methyl esters.

4. The method of claim 1 , wherein the solvent comprises glycerol and the monomers, oligomers, or both comprise glyceryl esters.

5. The method of claim 1 , wherein the second pressure is sufficiently high to maintain at least a portion of the solvent in a liquid phase at the second temperature.

6. The method of claim 1 , wherein the monomers, oligomers, or both comprise one or more compounds of Formula I:

wherein:

R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , R 7 , R 8 , R 9 , and R 10 are each independently —H, —OR 13 , —NR 13 R 14 , —SR 13 , halogen, —C 1 -C 6 alkyl, —C 1 -C 6 alkenyl, —C 1 -C 6 alkynyl, —C 3 -C 7 cycloalkyl, aryl, or 5- to 10-membered ring heteroaryl, wherein each alkyl, alkenyl, alkynyl, cycloalkyl, aryl, or heteroaryl is optionally substituted with —OR 13 , —NR 13 R 14 , —SR 13 , or halogen;

R 13 and R 14 are each independently —H, —C 1 -C 6 alkyl, —C 1 -C 6 alkenyl, or —C 1 -C 6 alkynyl;

R 11 is —H, -glyceryl, —C 1 -C 6 alkyl, —C 1 -C 6 alkenyl, —C 1 -C 6 alkynyl, —C 3 -C 7 cycloalkyl, aryl, or 5- to 10-membered ring heteroaryl, wherein each alkyl, alkenyl, alkynyl, cycloalkyl, aryl, or heteroaryl is optionally substituted with —OR 13 , —NR 13 R 14 , —SR 13 , or halogen;

R 12 is —OH, —H, —C 1 -C 6 alkyl, —C 1 -C 6 alkenyl, —C 1 -C 6 alkynyl, —C 3 -C 7 cycloalkyl, aryl, or 5- to 10-membered ring heteroaryl, wherein each alkyl, alkenyl, alkynyl, cycloalkyl, aryl, or heteroaryl is optionally substituted with —OR 13 , —NR 13 R 14 , —SR 13 , halogen, —COOH, or —COOR 11 ; and

m, n, and o are each independently an integer in the range of 0 to 30, and 0≤m+n+o≤30.

7. The method of claim 1 , wherein the mixture is substantially free of added acid or base.

8. The method of claim 1 , further comprising chemically modifying at least some of the esters.

9. The method of claim 8 , wherein the chemically modifying comprises transesterifying.

10. A method of preparing a composition comprising monomers, oligomers, or both derived from cutin, the method comprising:

combining cutin-containing plant matter with a solvent to yield a mixture, wherein the solvent comprises a nucleophilic solvent, and has a boiling point at a first temperature at a first pressure of one atmosphere;

increasing the temperature of the mixture to a second temperature and the pressure of the mixture to a second pressure to yield a composition comprising monomers, oligomers, or both derived from cutin, wherein the second temperature is greater than the first temperature, the second pressure is greater than one atmosphere, and the monomers, oligomers, or both comprise esters; and

chemically modifying at least some of the monomers, oligomers, or both.

11. The method of claim 10 , wherein the solvent comprises water, ethanol, methanol, or glycerol.

12. The method of claim 10 , wherein the solvent comprises water, and the monomers, oligomers, or both comprise fatty acid monomers, oligomers of the fatty acid monomers, or both.

13. The method of claim 12 , wherein the second pressure is sufficiently high to maintain at least a portion of the water in a liquid phase at the second temperature.

14. The method of claim 13 , wherein the second temperature is at least 393 K.

15. The method of claim 12 , wherein the chemically modifying comprises chemically modifying at least some of the fatty acid monomers, oligomers of the fatty acid monomers, or both.

16. The method of claim 15 , wherein the chemically modifying comprises esterifying at least some of the fatty acid monomers, oligomers of the fatty acid monomers, or both.

17. The method of claim 10 , wherein the monomers, oligomers, or both comprise one or more compounds of Formula I:

wherein:

R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , R 7 , R 8 , R 9 , and R 10 are each independently —H, —OR 13 , —NR 13 R 14 , —SR 13 , halogen, —C 1 -C 6 alkyl, —C 1 -C 6 alkenyl, —C 1 -C 6 alkynyl, —C 3 -C 7 cycloalkyl, aryl, or 5- to 10-membered ring heteroaryl, wherein each alkyl, alkenyl, alkynyl, cycloalkyl, aryl, or heteroaryl is optionally substituted with —OR 13 , —NR 13 R 14 , —SR 13 , or halogen;

R 13 and R 14 are each independently —H, —C 1 -C 6 alkyl, —C 1 -C 6 alkenyl, or —C 1 -C 6 alkynyl;

R 11 is —H, -glyceryl, —C 1 -C 6 alkyl, —C 1 -C 6 alkenyl, —C 1 -C 6 alkynyl, —C 3 -C 7 cycloalkyl, aryl, or 5- to 10-membered ring heteroaryl, wherein each alkyl, alkenyl, alkynyl, cycloalkyl, aryl, or heteroaryl is optionally substituted with —OR 13 , —NR 13 R 14 , —SR 13 , or halogen;

R 12 is —OH, —H, —C 1 -C 6 alkyl, —C 1 -C 6 alkenyl, —C 1 -C 6 alkynyl, —C 3 -C 7 cycloalkyl, aryl, or 5- to 10-membered ring heteroaryl, wherein each alkyl, alkenyl, alkynyl, cycloalkyl, aryl, or heteroaryl is optionally substituted with —OR 13 , —NR 13 R 14 , —SR 13 , halogen, —COOH, or —COOR 11 ; and

m, n, and o are each independently an integer in the range of 0 to 30, and 0≤m+n+o≤30.

18. The method of claim 10 , wherein the mixture is substantially free of added acid or base.

Assignments (3)
TERMINATION AND RELEASE OF INTELLECTUAL PROPERTY SECURITY AGREEMENT AT REEL/FRAME NO. 60562/0503 Recorded Dec 15, 2023
From: SLR INVESTMENT CORP., AS AGENT
To: APEEL TECHNOLOGY, INC.
Reel/Frame 066045/0001 →
SECURITY INTEREST Recorded Jul 1, 2022
From: APEEL TECHNOLOGY, INC.
To: SLR INVESTMENT CORP., AS COLLATERAL AGENT
Reel/Frame 060562/0503 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 16, 2021
From: BAKUS, RONALD C, II; PEREZ, LOUIS; MOL, CAMILLE; ROGERS, JAMES; RODRIGUEZ, GABRIEL
To: APEEL TECHNOLOGY, INC.
Reel/Frame 056569/0161 →
Continuity (6)
Continuation 16692807 · Nov 22, 2019
Continuation 15943553 · Apr 2, 2018
Continuation 15680541 · Aug 18, 2017
Continuation PCTUS2016065917 · Dec 9, 2016
Provisional Application 62265726 · Dec 10, 2015
Related Publication 20210291074A1 · Sep 23, 2021