IP Library Granted Patent US 7,790,701
Granted Patent B2
US 7,790,701 · App. 11/788,114 · Granted Sep 7, 2010

Silicon-based tocopherol derivatives

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Quick Facts
Patent No.
US 7,790,701
App. No.
11/788,114
Granted
Sep 7, 2010
Kind
B2
Abstract

Silicon-based tocopherol derivatives are provided, as well as methods for making the same, in which the derivatives have a tocopherol molecule having a silicon-based group. The derivatives are useful in cosmetic compositions, have antioxidant properties, enhance solubility and compatibility in cosmetic formulations having silicon-based materials within the compositions.

Claims (22)

1. A silicon-based tocopherol derivative represented by the formula V and by the formula VI, wherein the structure of formula (V) is:

wherein n=0 or 1, wherein each of R 1 , R 2 and R 3 are selected from hydrogen and CH 3 and at least one of R 1 , R 2 and R 3 is CH 3 ;

R 4 is (CH 2 CH 2 CH 2 CH(CH 3 )) 3 CH 3 , or (CH 2 CH 2 CH═C(CH 3 )) 3 CH 3 ; and each R 5 group is independently selected to be a straight or branched chain group of from one to 10 carbon atoms selected from the group consisting of alkyl, alkenyl, alkoxy, alkenoxy, silyl, siloxy, alkylsilyl, alkenylsilyl, alkylsiloxy and alkenylsiloxy or a straight or branched chain silicone polymer which may have one or more oxygen molecules in the chain; and the structure of formula VI is:

wherein R 1 , R 2 and R 3 are independently selected from hydrogen, —CH 3 , —Si(R 6 ) p , —OSi(R 5 ) p , —R 5 Si(R 5 ) p , and —R 5 OSi(R 5 ) p , wherein at least one of R 1 , R 2 and R 3 is —Si(R 6 ) p , —OSi(R 5 ) p , —R 5 Si(R 5 ) p or —R 5 OSi(R 5 ) p , and p is 3;

R 4 is (CH 2 CH 2 CH 2 CH(CH 3 )) 3 CH 3 or (CH 2 CH 2 CH═C(CH 3 )) 3 CH 3 ; each R 5 group is independently selected to be either R 6 or, a substituted or unsubstituted, saturated or unsaturated, methyl group; and

each R 6 group is independently selected to be hydrogen or a straight or branched chain group of from two to 10 carbon atoms selected from the group consisting of alkyl, alkenyl, alkoxy, alkenoxy, silyl, siloxy, alkylsilyl, alkenylsilyl, alkylsiloxy and alkenylsiloxy or a straight or branched chain silicone polymer which may have one or more oxygen molecules in the chain.

2. The silicon-based tocopherol derivative according to claim 1 , wherein the compound remains chemically stable until exposed to hydrolysis upon application to the skin wherein the tocopherols which act as antioxidants are liberated.

3. The silicon-based tocopherol derivative according to claim 1 , wherein the derivative is selected from the group consisting of 3-(DL-tocopheroloxypropyl)heptamethyltrisiloxane, 3-(DL-tocopheroloxy)heptamethyltrisiloxane, DL-tocopheroloxypropyltriethoxysilane, and DL-tocopheroloxypropyl-terminated polydimethylsiloxane.

4. The silicon-based tocopherol derivative according to claim 1 , wherein the derivative is selected from the group consisting of 5-bis(trimethylsiloxy)methylsilylpropyl-7-methyl-α-tocopherol and 5-methyl-7-bis(trimethylsiloxy)methylsilylpropyl-α-tocopherol.

5. A cosmetic composition comprising:

a cosmetic base formulation, and

at least one silicon-based tocopherol derivative represented by the formula V and by the formula VI, wherein:

the structure of formula (V) is:

wherein n=0 or 1, wherein each of R 1 , R 2 and R 3 are selected from hydrogen and CH 3 and at least one of R 1 , R 2 and R 3 is CH 3 ;

R 4 is (CH 2 CH 2 CH 2 CH(CH 3 )) 3 CH 3 , or (CH 2 CH 2 CH═C(CH 3 )) 3 CH 3 ; and each R 5 group is independently selected to be a straight or branched chain group of from one to 10 carbon atoms selected from the group consisting of alkyl, alkenyl, alkoxy, alkenoxy, silyl, siloxy, alkylsilyl, alkenylsilyl, alkylsiloxy and alkenylsiloxy or a straight or branched chain silicone polymer which may have one or more oxygen molecules in the chain; and the structure of formula VI is:

wherein R 1 , R 2 and R 3 are independently selected from hydrogen, —CH 3 , —Si(R 6 ) p , —OSi(R 5 ) p , —R 5 Si(R 5 ) p , and —R 5 OSi(R 5 ) p , wherein at least one of R 1 , R 2 and R 3 is —Si(R 6 ) p , —OSi(R 5 ) p , —R 5 Si(R 5 ) p or —R 5 OSi(R 5 ) p , and p is 3;

R 4 is (CH 2 CH 2 CH 2 CH(CH 3 )) 3 CH 3 or (CH 2 CH 2 CH═C(CH 3 )) 3 CH 3 ; each R 5 group is independently selected to be either R 6 or, a substituted or unsubstituted, saturated or unsaturated, methyl group; and

each R 6 group is independently selected to be hydrogen or a straight or branched chain group of from two to 10 carbon atoms selected from the group consisting of alkyl, alkenyl, alkoxy, alkenoxy, silyl, siloxy, alkylsilyl, alkenylsilyl, alkylsiloxy and alkenylsiloxy or a straight or branched chain silicone polymer which may have one or more oxygen molecules in the chain.

6. The cosmetic composition according to claim 5 , wherein the silicon-based tocopherol is selected from the group consisting of 3-(DL-tocopheroloxypropyl)heptamethyltrisiloxane, 3-(DL-tocopheroloxy)heptamethyltrisiloxane, DL-tocopheroloxypropyltriethoxysilane, and DL-tocopheroloxypropyl-terminated polydimethylsiloxane.

7. The cosmetic formulation according to claim 5 , wherein the formulation is selected from the group consisting of creams, lotions, sunscreens, lipsticks, cream eyeshadows, blush, antiaging creams, sunburn creams, self-tanning lotions, foundation and hair cosmetics.

8. The cosmetic formulation according to claim 5 , wherein the cosmetic base formulation comprises a silicone polymer or a silane-based compound.

9. The cosmetic composition according to claim 5 , wherein the silicon-based tocopherol derivative is selected from the group consisting of 5-bis(trimethylsiloxy)methylsilylpropyl-7-methyl-α-tocopherol and 5-methyl-7-bis(trimethylsiloxy)methylsilylpropyl-α-tocopherol.

Assignments (9)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 22, 2024
From: GELEST TECHNOLOGIES, INC.
To: GELEST, INC.
Reel/Frame 068467/0243 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 10, 2022
From: GELEST TECHNOLOGIES, INC.
To: GELEST, INC.
Reel/Frame 058668/0350 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 28, 2021
From: GELEST TECHNOLOGIES, INC.
To: GELEST, INC.
Reel/Frame 058595/0701 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 7, 2021
From: GELEST TECHNOLOGIES, INC.
To: GELEST, INC.
Reel/Frame 056272/0183 →
RELEASE OF SECURITY INTEREST Recorded Oct 1, 2020
From: ANTARES CAPITAL LP
To: GELEST BIOSYSTEMS, LLC; GELEST, INC.; GELEST TECHNOLOGIES, INC.
Reel/Frame 053946/0556 →
RELEASE OF SECURITY INTEREST Recorded Jun 24, 2019
From: WELLS FARGO BANK, NATIONAL ASSOCIATION
To: GELEST TECHNOLOGIES, INC.; GELEST, INC.; GELEST BIOSYSTEMS, LLC
Reel/Frame 049567/0194 →
PATENT SECURITY AGREEMENT Recorded Jun 21, 2019
From: GELEST, INC.; GELEST TECHNOLOGIES, INC.; GELEST BIOSYSTEMS, LLC
To: ANTARES CAPITAL LP
Reel/Frame 049557/0526 →
SECURITY INTEREST Recorded Aug 14, 2017
From: GELEST, INC.; GELEST TECHNOLOGIES, INC.; GELEST BIOSYSTEMS, LLC
To: WELLS FARGO BANK, NATIONAL ASSOCIATION
Reel/Frame 043540/0963 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 13, 2007
From: ARKLES, BARRY C.; PAN, YOULIN; HOLLENBERG, JANE C.
To: GELEST TECHNOLOGIES, INC.
Reel/Frame 019554/0390 →