IP Library Granted Patent US 6,962,692
Granted Patent B2
US 6,962,692 · App. 10/385,833 · Granted Nov 8, 2005

Photostabilizers, UV absorbers, and methods of photostabilizing a sunscreen composition

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 6,962,692
App. No.
10/385,833
Granted
Nov 8, 2005
Kind
B2
Abstract

Polymers and compounds including a diphenylmethylene or a 9H-fluorene moiety; and sunscreen compositions including a mixture of a photoactive compound and any one of the foregoing derivatives are disclosed herein. Also disclosed are methods for stabilizing a sunscreen composition by the addition of one or more of the foregoing derivatives, methods of filtering out ultra-violet light from a substrate by the use of one or more such derivatives, and methods for terminating a polymerization reaction by the addition of derivatives of diphenylmethylene and/or 9H-fluorene. Synergistic combinations of the polymer with (1) diesters or polyesters of a naphthalene dicarboxylic acid, or (2) oxybenzone enhance the photostability of sunscreen compositions containing a photodegradable sunscreen active compound, such as avobenzone.

Claims (41)

1. A sunscreen composition, comprising a mixture of a photoactive compound; about 0.1% to about 15% by weight of a compound selected from the group consisting of compounds of formula (IX), compounds of formula (X), and combinations thereof:

wherein R 19 , R 20 , R 21 , R 24 , R 25 , R 26 , R 29 , R 30 , R 31 , and R 32 are the same or different and are selected from the group consisting of C 1 -C 30 alkyl, C 3 -C 8 cycloalkyl, substituted alkyl, substituted cycloalkyl, ester, aryl, heteroaryl, heterocycloalkyl, substituted aryl, substituted heteroaryl, substituted heterocycloalkyl, and amino; R 17 and R 23 are the same or different and are selected from the group consisting of C 1 -C 30 alkyl, C 3 -C 8 cycloalkyl, substituted alkyl, substituted cycloa 1 kyl, ester, aryl, heteroaryl, heterocycloalkyl, substituted aryl, substituted heteroaryl, substituted heterocycloalkyl, cyano, and amino; R 18 and R 22 are the same or different and are selected from the group consisting of substituted diphenylmethylene, unsubstitilted diphenylmethylene, substituted 9H-fluorene, and unsubstituted 9H-fluorene; t and u are each in the range of 1 to 100; s is in the range of 0 to 100; and a, b, c, and d are each in the range of 0 to 4; and about 2% to about 15% by weight of a diester or polyester of naphthalene dicarboxylic acid selected from the group consisting of compounds of formula (VII), formula (VIII), and combinations thereof:

wherein R 13 and R 14 are the same or different and selected from the group consisting of C 1 -C 22 alkyl groups, diols having the structure HO—R 15 —OH, and polyglycols having the structure HO—R 16 —(—O—R 15 —) n —OH; wherein each R 15 and R 16 is the same or different and selected from the group consisting of C 1 -C 6 straight or branched chain alkyl groups; and wherein m and n are each in a range of 1 to 100 and p is in a range of 0 to 100.

2. The composition of claim 1 , wherein R 19 , R 20 and R 21 are selected from the group consisting of C 1 -C 15 branched chain alkyls.

3. The composition of claim 1 , wherein R 17 and R 23 are the same and are cyano and R 18 and R 22 are the same and are diphenylmethylene.

4. The composition of claim 1 , wherein the composition includes one or more compounds of formula (IX) or (X) or a combination of (IX) and (X) in a weight ratio to one or more compounds of formula (VII) or (VIII) or a combination of (VII) and (VIII) in the range of 0.02 to 5.0.

5. The composition of claim 4 , wherein said weight ratio is in the range of 0.02 to 1.5.

6. The composition of claim 5 , wherein said weight ratio is in the range of 0.05 to 1.0.

7. The composition of claim 6 , wherein said weight ratio is in the range of 0.1 to 0.75.

8. The composition of claim 1 , including an effective amount of a photoactive compound selected from the group consisting of p-aminobenzoic acid and salts and derivatives thereof; anthranilate and derivatives thereof; dibenzoylmethane and derivatives thereof; salicylate and derivatives thereof; cinnamic acid and derivatives thereof; dihydroxycinnamic acid and derivatives thereof; camphor and salts and derivatives thereof; trihydroxycinnamic acid and derivatives thereof; dibenzalacetone naphtholsulfonate and salts and derivatives thereof; benzalacetophenone naphtholsulfonate and salts and derivatives thereof; dihydroxy-naphthoic acid and salts thereof; o-hydroxydiphenyldisulfonate and salts and derivatives thereof; p-hydroxydiphenyldisulfonate and salts and derivatives thereof; coumarin and derivatives thereof; diazole derivatives; quinine derivatives and salts thereof; quinoline derivatives; hydroxy-substituted benzophenone derivatives; methoxy-substituted benzophenone derivatives; uric acid derivatives; vilouric acid derivatives; tannic acid and derivatives thereof; hydroquinone; benzophenone derivatives; 1,3,5-triazine derivatives; phenyldibenzimidazole tetrasulfonate and salts and derivatives thereof; terephthalylidene dicamphor sulfonic acid and salts and derivatives thereof; methylene bis-benzotriazolyl tetramethylbutylphenol and salts and derivatives thereof; bis-ethylhexyloxyphenol methoxyphenyl triazine and salts and derivatives thereof; diethylamino hydroxybenzoly hexyl benzoate and salts and derivatives thereof; and combinations of the foregoing.

9. The composition of claim 8 , wherein the photoactive compound is a dibenzoylmethane derivative.

10. The composition of claim 9 , wherein the dibenzoylmethane derivative is selected from the group consisting of 2-methyldibenzoylmetane; 4-methyldibenzoylmethane; 4-isopropyldibenzoylmethane; 4-tert-methlydibenzoylmethane; 2,4-dimethyldibenzoylmethane; 2,5-dimethyldibenzoylmethane; 4,4-diisopropyldibenzoylmethane; 4,4′-dimethoxydibenzoylmethane, 4-tert-butyl-4′-methyoxydibenzoylmethane; 2-methyl-5-isopropyl-4′-methyoxydibenzoylmethane; 2-methyl-5-tert-butyl-4′-methyoxydibenzoylmethane; 2,4-dimethyl-4′-methyoxydibenzoylmethane; 2,6-dimethyl-4-tert-butyl-4-′-methyoxydibenzoylmethane, and combinations thereof.

11. The composition of claim 1 , comprising a diester of formula (VIII) wherein R 1 and R 2 are 2-ethylhexane and p is 0.

12. A method of protecting human skin from ultraviolet radiation comprising topically applying to said skin, in a cosmetically acceptable carrier, the composition of claim 1 .

13. The method of claim 12 , wherein R 19 , R 20 and R 21 are selected from the group consisting of C 1 -C 15 branched chain alkyls.

14. The method of claim 12 , wherein R 17 and R 23 are the same and are cyano; R 18 and R 22 are the same and are diphenylmethylene; R 20 is C 4 H 8 ; t=1; R 19 and R 21 are C 3 H 9 ; and s=1-5.

15. The method of claim 12 , wherein the composition includes one or more compounds of formula (IX) or (X) or a combination of (IX) and (X) in a weight ratio to one or more compounds of formula (VII) or (VIII) or a combination of (VII) and (VIII) in the range of 0.02 to 5.0.

16. The method of claim 15 , wherein said weight ratio is in the range of 0.02 to 1.5.

17. The method of claim 12 , wherein the composition includes a photoactive compound selected from the group consisting of p-aminobenzoic acid and salts and derivatives thereof; anthranilate and derivatives thereof; dibenxoylmethane and derivatives thereof; salicylate and derivatives thereof; cinnamic acid and derivatives thereof; dihydroxycinnamic acid and derivatives thereof; camphor and salts and derivatives thereof; trihydroxycinnamic acid and derivatives thereof; dibenzalacetone naphtholsulfonate and salts and derivatives thereof; benzalacetophenone naphtholsulfonate and salts and derivatives thereof; dihydroxy-naphthoic acid and salts thereof; o-hydroxydiphenyldisulfonate and salts and derivatives thereof; p-hyroxydiphenyldisulfonate and salts and derivatives thereof; coumarin and derivatives thereof; diazole derivatives; quinine derivatives and salts thereof; quinoline derivatives; hydroxy-substituted benzophenone derivatives; methoxy-substituted benzophenone derivatives; uric acid derivatives; vilouric acid derivatives; tannic acid and derivatives thereof; hydroquinone; benzophenone derivatives; 1,3,5-triazine derivatives; phenyldibenzimidazole tetrasulfonate and salts and derivatives thereof; terephthalylidene dicamphor sulfonic acid and salts and derivatives thereof; methylene bis-benzotriazolyl tetramethylbutylphenol and salts and derivatives thereof; bis-ethylhexyloxyphenol methoxyphenyl triazine and salts and derivatives thereof; diethylamino hydroxybenzoyl hexyl benzoate and salts and derivatives thereof; and combinations of the foregoing.

18. The method of claim 17 , wherein the composition includes a dibenzoylmethane derivative.

19. A method of protecting human skin from ultraviolet radiation comprising topically applying to said skin, a composition comprising about 0.1% to about 25% by weight of a compound selected from the group consisting of compounds of formula (IX), compounds of formula (X), and combinations thereof:

wherein, R 19 , R 20 , R 21 , R 24 , R 25 , R 26 , R 29 , R 30 , R 31 , and R 32 are the same or different and are selected from the group consisting of C 1 -C 30 alkyl, C 3 -C 8 cycloalkyl, substituted alkyl, substituted cycloalkyl, ester, aryl, heteroaryl, heterocycloalkyl, substituted aryl, substituted heteroaryl, substituted heterocycloalkyl, and amino; R 17 and R 23 are the same or different and are selected from the group consisting of C 1 -C 30 alkyl, C 3 -C 8 cycloalkyl, substituted alkyl, substituted cycloalkyl, ester, aryl, heteroaryl, heterocycloalkyl, substituted aryl, substituted heteroaryl, substituted beterocycloalkyl, cyano, and amino; R 18 and R 22 are the same or different and are selected from the group consisting of substituted diphenylmethylene, unsubstituted diphenylmethylene, substituted 9H-fluorene, and unsubstituted 9H-fluorene; t and u are each in the range of 1 to 100; s is in the range of 0 to 100; and a, b, c, and d are each in the range of 0 to 4.

20. A sunscreen composition, comprising a mixture of a photoactive compound; about 0.1% to about 15% by weight of a compound selected from the group consisting of compounds of formula (IX), compounds of formula (X), and combinations thereof:

wherein, R 19 , R 20 , R 21 , R 24 , R 25 , R 26 , R 29 , R 30 , R 31 , and R 32 are the same or different and are selected from the group consisting of C 1 -C 30 alkyl, C 3 -C 8 cycloalkyl, substituted alkyl, substituted cycloalkyl, ester, aryl, heteroaryl, heterocycloalkyl, substituted aryl, substituted heteroaryl, substituted heterocycloalkyl, and amino; R 17 and R 23 are the same or different and are selected from the group consisting of C 1 -C 30 alkyl, C 3 -C 8 cycloalkyl, substituted alkyl, substituted cycloalkyl, ester, aryl, heteroaryl, heterocycloalkyl, substituted aryl, substituted heteroaryl, substituted heterocycloalkyl, cyano, and amino; R 18 and R 22 are the same or different and are selected from the group consisting of substituted diphenylmethylene, unsubstituted diphenylmethylene, substituted 9H-fluorene, and unsubstituted 9H-fluorene; t and u are each in the range of 1 to 100; s is in the range of 0 to 100; and a, b, c, and d are each in the range of 0 to 4; and about 0.5% to about 15% of oxybenzone.

21. The composition of claim 20 , wherein R 19 , R 20 and R 21 are selected from the group consisting of C 1 -C 15 branched chain alkyls.

22. The composition of claim 20 , wherein R 17 and R 23 are the same and are cyano and R 18 and R 22 are the same and are diphenylmethylene.

23. The composition of claim 20 , wherein the composition includes one or more compounds of formula (IX) or (X) or a combination of (IX) and (X) in a weight ratio to oxybenzone in the range of 0.025 to 5.0.

24. The composition of claim 23 , wherein said weight ratio is in the range of 0.03 to 1.5.

25. The composition of claim 24 , wherein said weight ratio is in the range of 0.05 to 1.0.

26. The composition of claim 25 , wherein said weight ratio is in the range of 0.1 to 0.75.

27. The composition of claim 20 , including an effective amount of a photoactive compound selected from the group consisting of p-aminobenzoic acid and salts and derivatives thereof; anthranilate and derivatives thereof; dibenzoylmethane and derivatives thereof; salicylate and derivatives thereof; cinnamic acid and derivatives thereof; dihydroxycinnamic acid and derivatives thereof; camphor and salts and derivatives thereof; trihydroxycinnamic acid and derivatives thereof; dibenzalacetone naphtholsulfonate and salts and derivatives thereof; benzalacetophenone naphtholsulfonate and salts and derivatives thereof, dihydroxy-naphthoic acid and salts thereof; o-hydroxydiphenyldisulfonate and salts and derivatives thereof; p-hydroxydiphenyldisulfonate and salts and derivatives thereof; coumarin and derivatives thereof, diazole derivatives; quinine derivatives and salts thereof; quinoline derivatives; hydroxy-substituted beazophenone derivatives; methoxy-substituted benzophenone derivatives; uric acid derivatives; vilouric acid derivatives; tannic acid and derivatives thereof; hydroquinone; benzophenone derivatives; 1,3,5-triazine derivatives; phenyldibenzimidazole tetrasulfonate and salts and derivatives thereof; terephthalylidene dicamphor sulfonic acid and salts and derivatives thereof; methylene bis-benzotriazolyl tetramethylbutylphenol and salts and derivatives thereof; bis-ethylhexyloxyphenol methoxyphenyl triazine and salts and derivatives thereof; diethylamino hydroxybenzoyl hexyl benzoate and salts and derivatives thereof; and combinations of the foregoing.

28. The composition of claim 27 , wherein the photoactive compound is a dibenzoylmethane derivative.

29. The composition of claim 28 , wherein the dibenzoylmethane derivative is selected from the group consisting of 2-methyldibenzoylmethane; 4-methyldibenzoylmethane; 4-isopropyldibenzoylmethane; 4-tert-butyldibenzoylmethane; 2,4-dimelhyldibenzoyhnethane; 2,5-dimethyldibenzoylmethane; 4,4′-diisopropyldibenzoylmethane; 4,4′-dimethoxydibenzoylmethane; 4-tert-butyl-4′-methoxydibenzoylmethane; 2-methyl-5-isopropyl-4′-methoxydibenzoylmethane; 2-methyl-5-tert-butyl-4′-methoxydibenzoylmethane; 2,4-dimethyl-4′-methoxydibenzoylmethane; 2,6-dimethyl-4-tert-butyl-4′-methoxydibenzoylmethane, and combinations thereof.

30. A method ofprotecting human skin from ultraviolet radiation comprising topically applying to said skin, in a cosmetically acceptable carrier, the composition of claim 20 .

31. The method of claim 30 , wherein R 19 , R 20 and R 21 are selected from the group consisting of C 1 -C 15 branched chain alkyls.

32. The method of claim 30 , wherein R 17 and R 23 are the same and are cyano and R 18 and R 22 are the same and are diphenylmethylene.

33. The method of claim 30 , wherein the composition includes one or more compounds of formula (IX) or (X) or a combination of (IX) and (X) in a weight ratio to the weight of oxybenzone in the range of 0.025 to 5.0.

34. The method of claim 33 , wherein said weight ratio is in the range of 0.03 to 1.5.

35. The method of claim 30 , wherein the composition includes a photoactive compound selected from the group consisting of p-aminobenzoic acid and salts and derivatives thereof; anthranilate and derivatives thereof; dibenzoylmethane and derivatives thereof; salicylate and derivatives thereof; cinnamic acid and derivatives thereof; dihydroxycinnamic acid and derivatives thereof; camphor and salts and derivatives thereof; trihydroxycinnamic acid and derivatives thereof; dibenzalacetone naphtholsulfonate and salts and derivatives thereof; benzalacetophenone naphtholsulfonate and salts and derivatives thereof; dihydroxy-naphthoic acid and salts thereof; o-hydroxydiphenyldisulfonate and salts and derivatives thereof; p-hydroxydiphenyldisulfonate and salts and derivatives thereof; coumarin and derivatives thereof; diazole derivatives; quinine derivatives and salts thereof; quinoline derivatives; hydroxy-substituted benzophenone derivatives; methoxy-substituted benzophenone derivatives; uric acid derivatives; vilouric acid derivatives; tannic acid and derivatives thereof; hydroquinone; benzophenone derivatives; 1,3,5-triazine derivatives; phenyldibenzimidazole tetrasulfonate and salts and derivatives thereof; terephthalylidene dicamphor sulfonic acid and salts and derivatives thereof; methylene bis-benzotriazolyl tetramethylbutylphenol and salts and derivatives thereof; bis-ethylhexyloxyphenol methoxyphenyl triazine and salts and derivatives thereof; diethylamino hydroxybenzoyl hexyl benzoate and salts and derivatives thereof; and combinations of the foregoing.

36. The method of claim 35 , wherein the composition includes a dibenzoylmethane derivative.

37. A compound having the following structure:

Assignments (13)
THIRD AMENDED AND RESTATED INTELLECTUAL PROPERTY SECURITY AGREEMENT Recorded Dec 20, 2024
From: THE HALLSTAR COMPANY; HALLSTAR INNOVATIONS CORP.; HALLSTAR BEAUTY AND PERSONAL CARE INNOVATIONS COMPANY; UNIPLEX COMPANY
To: BANK OF AMERICA, N.A., AS ADMINISTRATIVE AGENT
Reel/Frame 069747/0045 →
THIRD AMENDED AND RESTATED INTELLECTUAL PROPERTY SECURITY AGREEMENT Recorded Nov 3, 2023
From: THE HALLSTAR COMPANY; HALLSTAR INNOVATIONS CORP.; HALLSTAR BEAUTY AND PERSONAL CARE INNOVATIONS COMPANY; UNIPLEX COMPANY
To: BANK OF AMERICA, N.A., AS ADMINISTRATIVE AGENT
Reel/Frame 065448/0262 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 28, 2018
From: HALLSTAR INNOVATIONS CORP.
To: HALLSTAR BEAUTY AND PERSONAL CARE INNOVATIONS COMPANY
Reel/Frame 046977/0359 →
SECOND AMENDED AND RESTATED INTELLECTUAL PROPERTY SECURITY AGREEMENT Recorded Nov 25, 2014
From: HALLSTAR INNOVATIONS CORP.
To: BANK OF AMERICA, N.A., AS AGENT
Reel/Frame 034468/0854 →
AMENDED AND RESTATED INTELLECTUAL PROPERTY SECURITY AGREEMENT Recorded Feb 21, 2012
From: HALLSTAR INNOVATIONS CORP.
To: BANK OF AMERICA, N.A., AS AGENT
Reel/Frame 027742/0917 →
SECURITY INTEREST Recorded Oct 16, 2008
From: HALLSTAR INNOVATIONS CORP.
To: LASALLE BANK NATIONAL ASSOCIATION, AS AGENT
Reel/Frame 021709/0286 →
INTELLECTUAL PROPERTY RELEASE Recorded Oct 14, 2008
From: LASALLE BANK NATIONAL ASSOCIATION, AS AGENT
To: HALLSTAR INNOVATIONS CORP.
Reel/Frame 021669/0701 →
CHANGE OF NAME Recorded May 14, 2007
From: CPH INNOVATIONS CORP.
To: HALLSTAR INNOVATIONS CORP.
Reel/Frame 019287/0001 →
SECURITY AGREEMENT Recorded Jan 25, 2006
From: CPH INNOVATIONS CORP.
To: LASALLE BANK NATIONAL ASSOCIATION, AS AGENT
Reel/Frame 017207/0546 →
CORRECTED COVER SHEET TO CORRECT ASSIGNEE NAME, PREVIOUSLY RECORDED AT REEL/FRAME 014788/0189 (ASSIGNMENT OF ASSIGNOR'S INTEREST) Recorded Apr 6, 2005
From: C.P. HALL COMPANY, THE
To: CPH INNOVATIONS CORP.
Reel/Frame 016427/0459 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 8, 2004
From: CPH INNOVATIONS CORP.
To: LASALLE BANK NATIONAL ASSOCIATION
Reel/Frame 015246/0708 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 29, 2004
From: THE C.P. HALL COMPANY
To: CPH INNOVATIONS CORPORATION
Reel/Frame 014788/0189 →
SECURITY AGREEMENT Recorded Jan 2, 2004
From: C.P. HALL COMPANY, THE
To: LASALLE BANK NATIONAL ASSOCIATION
Reel/Frame 014227/0316 →