Preparation of an amino-functional polyorganosiloxane emulsion
US-2024335800-A1 · Oct 10, 2024 · US
US9757313B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9757313-B2 |
| Application number | US-21225308-A |
| Country | US |
| Kind code | B2 |
| Filing date | Sep 17, 2008 |
| Priority date | Sep 24, 2007 |
| Publication date | Sep 12, 2017 |
| Grant date | Sep 12, 2017 |
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A cosmetic or dermatological compositions of oil-in-water emulsion type, including, in a physiologically acceptable medium, at least gemini surfactant of formula (I): in which R 1 and R 3 denote, independently of one another, an alkyl radical containing from 1 to 25 carbon atoms; R 2 denotes a spacer consisting of a linear or branched alkylene chain containing from 1 to 12 carbon atoms; X and Y denote, independently of one another, a group —(C 2 H 4 O) a —(C 3 H 6 O) b Z; n ranges from 1 to 10, in combination with an effective amount of at least one semi-crystalline polymer which is solid at ambient temperature and which has a melting point below 70° C., said polymer having a number-average molecular mass greater than or equal to 2000, said emulsion having a proportion of fatty phase of greater than 10% by weight relative to the total weight of the composition and including more than 40% by weight of non-volatile oil(s) relative to the weight of the fatty phase.
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The invention claimed is: 1. A cosmetic or dermatological composition of oil-in-water type comprising, in a physiologically acceptable medium, at least one gemini surfactant of formula (I): in which: R 1 and R 3 denote, independently of one another, an alkyl radical containing from 1 to 25 carbon atoms; R 2 denotes a spacer consisting of a linear or branched alkylene chain containing from 1 to 12 carbon atoms; X and Y denote, independently of one another, a —(C 2 H 4 O) a —(C 3 H 6 O) b Z group where: Z denotes a hydrogen atom or a radical —CH 2 —COOM, —SO 3 M, —P(O)(OM) 2 , —C 2 H 4 —SO 3 M, —C 3 H 6 —SO 3 M, or —CH 2 (CHOH) 4 CH 2 OH, where M, M′ represent H or an alkali metal ion, an alkaline earth metal ion, an ammonium ion or alkanolammonium ion, a ranges from 0 to 15, b ranges from 0 to 10, and the sum of a +b ranges from 1 to 25; and n ranges from 1 to 10, in combination with an effective amount of at least one semi-crystalline homopolymer which is solid at ambient temperature and which has a melting point of below 70° C., comprising: a) a polymeric backbone, and b) at least one crystallizable organic side chain, said homopolymer having a number-average molecular mass greater than or equal to 2000, and said semi-crystalline homopolymer resulting from the polymerization of only monomers comprising a crystallizable chain, selected from the group consisting of C14-C24 alkyl (meth)acrylates, said composition having a proportion of fatty phase greater than 10% by weight relative to a total weight of said composition and comprising more than 40% by weight of non-volatile oil(s) relative to a total weight of the fatty phase, wherein the gemini surfactant is present at a content ranging from 0.01% to 5% by weight, relative to a total weight of the composition. 2. The composition according to claim 1 , wherein each of the groups R 1 —CO— and R 3 —CO— denotes a coconut fatty acid residue. 3. The composition according to claim 1 , wherein, for the gemini surfactant of formula (I), for each of the radicals X and Y, the sum of a and b has a mean value ranging from 10 to 20. 4. The composition according to claim 1 , wherein, for the gemini surfactant of formula (I), Y is the group —SO 3 M where M is an alkali metal ion. 5. The composition according to claim 1 , wherein, for the gemini surfactant of formula (I), n is equal to 1. 6. The composition according to claim 1 , wherein the surfactant of formula (I) has the following structure: 7. The composition according to claim 1 , wherein the gemini surfactant is mixed with (a) a glyceryl ester of a C 6 -C 22 fatty acid, (b) a glycerol diester of a C 6 -C 22 fatty acid and of citric acid, and (c) a C 10 -C 30 fatty alcohol. 8. The composition according to claim 1 , wherein the gemini surfactant is present at a content ranging from 0.2% to 1.5% by weight relative to a total weight of the composition. 9. The composition according to claim 1 , wherein the polymer has a number-average molecular mass ranging from 3000 to 500,000. 10. The composition according to claim 1 , wherein the polymer is soluble in the fatty phase to at least 1% by weight at a temperature above its melting point. 11. The composition according to claim 1 , wherein the polymer has a melting point Tm such that 30° C.≦Tm<50° C. 12. The composition according to claim 1 , containing at least one organic UV screen. 13. A cosmetic method for making up and/or for the non therapeutic care of keratin materials, comprising at least a step of applying to keratin materials a composition according to claim 1 . 14. The composition according to claim 4 , wherein M is a sodium ion. 15. The composition according to claim 1 , wherein the gemini surfactant is present at a content ranging from 0.1% to 3% by weight, relative to a total weight of the composition.
Emulsions · CPC title
Derivatives containing from 2 to 10 oxyalkylene groups · CPC title
Topical preparations for affording protection against sunlight or other radiation; Topical sun tanning preparations · CPC title
Homopolymers or copolymers of esters, e.g. (meth)acrylic acid esters; Compositions of derivatives of such polymers · CPC title
Preparations for care of the skin · CPC title
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