Cosmetic composition comprising hydrophilic antioxidants and thiopyridinone compounds
AssigneeL'oreal
InventorsNicholas David STEBBINS, David CHAN
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Abstract
The instant disclosure relates to cosmetic compositions comprising: (i) compounds of Thiopyridinone type; (ii) one or more hydrophilic antioxidants; and wherein the compound of thiopyridinone type and the one or more hydrophilic antioxydants are present in the composition in amounts sufficient to produce stability of (i) and (ii).
Claims19
A cosmetic composition comprising:
- i) at least one compound selected from compounds of formula (I) and tautomer of formula (I′) herein below or their salts;
- and their optical isomers, racemates, and/or solvates such as hydrates, alone or as a mixture:
- In which Formulas (I) and (I′):
- R1 denotes a radical chosen from:
- a) a hydrogen atom;
- b) a saturated linear C1-C10 or branched C3-C10 alkyl group optionally substituted with one or more groups, which may be identical or different, chosen from:
- i)—O—R3
- ii)—S—R3;
- R2 denotes a radical chosen from:
- a) a hydrogen atom;
- b) a saturated hydrocarbonated group linear C1-C12 or branched C3-C12 or cyclic C3-C8, optionally substituted with one or more groups, which may be identical or different, chosen from:
- i)—O—R3
- ii)—S—R3;
- iii)—C(O)—O—R3;
- iv) a C5-C12 aryl group optionally substituted with one or more hydroxyls and/or with one or more C1-C8 alkoxy radicals;
- c) a C5-C12 aryl group optionally substituted with one or more hydroxyls and/or with one or more C1-C8 alkoxy radicals
- R3 denotes a radical chosen from:
- a) a hydrogen atom;
- b) a saturated linear C1-C10 or branched C3-C10 alkyl group;
- ii) one or more hydrophilic antioxidants.
The composition of claim 11, wherein the ii) one or more ascorbic acid and its derivatives is present from about 0.1 to about 20 wt. %, based on the total weight of the cosmetic composition.
A cosmetic composition comprising:
- i) from about 0.01 to about 10 wt. % of at least one compound selected from compounds of formula (I) and tautomer of formula (I′) herein below or their salts;
- and their optical isomers, racemates, and/or solvates such as hydrates, alone or as a mixture:
- In which Formulas (I) and (I′):
- R1 denotes a radical chosen from:
- a) a hydrogen atom;
- b) a saturated linear C1-C10 or branched C3-C10 alkyl group optionally substituted with one or more groups, which may be identical or different, chosen from:
- i)—O—R3
- ii)—S—R3;
- R2 denotes a radical chosen from:
- a) a hydrogen atom;
- b) a saturated hydrocarbonated group linear C1-C12 or branched C3-C12 or cyclic C3-C8, optionally substituted with one or more groups, which may be identical or different, chosen from:
- i)—O—R3
- ii)—S—R3
- iii)—C(O)—O—R3;
- iv) a C5-C12 aryl group optionally substituted with one or more hydroxyls and/or with one or more C1-C8 alkoxy radicals;
- c) a C5-C12 aryl group optionally substituted with one or more hydroxyls and/or with one or more C1-C8 alkoxy radicals
- R3 denotes a radical chosen from:
- a) a hydrogen atom;
- b) a saturated linear C1-C10 or branched C3-C10 alkyl group;
- ii) from about 0.1 to about 20 wt. % of one or more hydrophilic antioxidant;
- and
- iii) a cosmetic suitable carrier;
- wherein the i) compound of thiopyridininone type and the ii) one or more hydrophilic antioxidants are present in the composition in amounts sufficient to produce stability of i) and ii);
- and
- wherein the weight percentages are based on the total weight of the cosmetic composition.
A method for stabilizing compound of thiopyridininone type and hydrophilic antioxidant when both present in a composition, in an amount sufficient to produce stability of compound of thiopyridininone type and hydrophilic antioxidant.
Dependencies are inferred from the claim text.