FR2882927A1 - Compositions cosmetiques solaires - Google Patents
Compositions cosmetiques solaires Download PDFInfo
- Publication number
- FR2882927A1 FR2882927A1 FR0502362A FR0502362A FR2882927A1 FR 2882927 A1 FR2882927 A1 FR 2882927A1 FR 0502362 A FR0502362 A FR 0502362A FR 0502362 A FR0502362 A FR 0502362A FR 2882927 A1 FR2882927 A1 FR 2882927A1
- Authority
- FR
- France
- Prior art keywords
- composition according
- composition
- derivatives
- ethylhexyl
- agent
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 54
- 239000002537 cosmetic Substances 0.000 title claims abstract description 20
- 239000003795 chemical substances by application Substances 0.000 title claims abstract description 18
- 230000005855 radiation Effects 0.000 title claims abstract description 18
- 239000002904 solvent Substances 0.000 title claims abstract description 15
- YBGZDTIWKVFICR-JLHYYAGUSA-N Octyl 4-methoxycinnamic acid Chemical compound CCCCC(CC)COC(=O)\C=C\C1=CC=C(OC)C=C1 YBGZDTIWKVFICR-JLHYYAGUSA-N 0.000 title claims abstract description 8
- 210000004209 hair Anatomy 0.000 title description 3
- 239000007787 solid Substances 0.000 claims abstract description 15
- 230000003711 photoprotective effect Effects 0.000 claims description 15
- 239000000839 emulsion Substances 0.000 claims description 10
- 239000000049 pigment Substances 0.000 claims description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 6
- -1 2-5 ethylhexyl-p-methoxycinnamate Chemical compound 0.000 claims description 5
- DXGLGDHPHMLXJC-UHFFFAOYSA-N oxybenzone Chemical compound OC1=CC(OC)=CC=C1C(=O)C1=CC=CC=C1 DXGLGDHPHMLXJC-UHFFFAOYSA-N 0.000 claims description 5
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 claims description 4
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N iron oxide Inorganic materials [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 claims description 3
- 229910044991 metal oxide Inorganic materials 0.000 claims description 3
- 150000004706 metal oxides Chemical class 0.000 claims description 3
- RVTZCBVAJQQJTK-UHFFFAOYSA-N oxygen(2-);zirconium(4+) Chemical class [O-2].[O-2].[Zr+4] RVTZCBVAJQQJTK-UHFFFAOYSA-N 0.000 claims description 3
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims description 3
- 229910001928 zirconium oxide Inorganic materials 0.000 claims description 3
- DSSYKIVIOFKYAU-XCBNKYQSSA-N (R)-camphor Chemical class C1C[C@@]2(C)C(=O)C[C@@H]1C2(C)C DSSYKIVIOFKYAU-XCBNKYQSSA-N 0.000 claims description 2
- ALYNCZNDIQEVRV-UHFFFAOYSA-N 4-aminobenzoic acid Chemical class NC1=CC=C(C(O)=O)C=C1 ALYNCZNDIQEVRV-UHFFFAOYSA-N 0.000 claims description 2
- 150000008366 benzophenones Chemical class 0.000 claims description 2
- 230000000903 blocking effect Effects 0.000 claims description 2
- NZZIMKJIVMHWJC-UHFFFAOYSA-N dibenzoylmethane Chemical class C=1C=CC=CC=1C(=O)CC(=O)C1=CC=CC=C1 NZZIMKJIVMHWJC-UHFFFAOYSA-N 0.000 claims description 2
- 238000009792 diffusion process Methods 0.000 claims description 2
- 150000003918 triazines Chemical class 0.000 claims description 2
- HEOCBCNFKCOKBX-UHFFFAOYSA-N 4,7,7-trimethyl-2-[(4-methylphenyl)methylidene]bicyclo[2.2.1]heptan-3-one Chemical compound C1=CC(C)=CC=C1C=C1C(=O)C2(C)CCC1C2(C)C HEOCBCNFKCOKBX-UHFFFAOYSA-N 0.000 claims 1
- 229910052684 Cerium Inorganic materials 0.000 claims 1
- GWXLDORMOJMVQZ-UHFFFAOYSA-N cerium Chemical compound [Ce] GWXLDORMOJMVQZ-UHFFFAOYSA-N 0.000 claims 1
- 235000013980 iron oxide Nutrition 0.000 claims 1
- VBMVTYDPPZVILR-UHFFFAOYSA-N iron(2+);oxygen(2-) Chemical class [O-2].[Fe+2] VBMVTYDPPZVILR-UHFFFAOYSA-N 0.000 claims 1
- SOQBVABWOPYFQZ-UHFFFAOYSA-N oxygen(2-);titanium(4+) Chemical class [O-2].[O-2].[Ti+4] SOQBVABWOPYFQZ-UHFFFAOYSA-N 0.000 claims 1
- 235000014692 zinc oxide Nutrition 0.000 claims 1
- RNWHGQJWIACOKP-UHFFFAOYSA-N zinc;oxygen(2-) Chemical class [O-2].[Zn+2] RNWHGQJWIACOKP-UHFFFAOYSA-N 0.000 claims 1
- 229910052721 tungsten Inorganic materials 0.000 description 10
- 210000003491 skin Anatomy 0.000 description 8
- 239000003921 oil Substances 0.000 description 6
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 5
- 239000004904 UV filter Substances 0.000 description 4
- RXKJFZQQPQGTFL-UHFFFAOYSA-N dihydroxyacetone Chemical compound OCC(=O)CO RXKJFZQQPQGTFL-UHFFFAOYSA-N 0.000 description 4
- 239000006185 dispersion Substances 0.000 description 4
- LXCFILQKKLGQFO-UHFFFAOYSA-N p-hydroxybenzoic acid methyl ester Natural products COC(=O)C1=CC=C(O)C=C1 LXCFILQKKLGQFO-UHFFFAOYSA-N 0.000 description 4
- 239000012071 phase Substances 0.000 description 4
- QELSKZZBTMNZEB-UHFFFAOYSA-N propylparaben Chemical compound CCCOC(=O)C1=CC=C(O)C=C1 QELSKZZBTMNZEB-UHFFFAOYSA-N 0.000 description 4
- 239000000725 suspension Substances 0.000 description 4
- 229920002125 Sokalan® Polymers 0.000 description 3
- 239000002304 perfume Substances 0.000 description 3
- 230000004224 protection Effects 0.000 description 3
- 238000005063 solubilization Methods 0.000 description 3
- 230000007928 solubilization Effects 0.000 description 3
- 239000001993 wax Substances 0.000 description 3
- ZAKOWWREFLAJOT-CEFNRUSXSA-N D-alpha-tocopherylacetate Chemical compound CC(=O)OC1=C(C)C(C)=C2O[C@@](CCC[C@H](C)CCC[C@H](C)CCCC(C)C)(C)CCC2=C1C ZAKOWWREFLAJOT-CEFNRUSXSA-N 0.000 description 2
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
- 241001465754 Metazoa Species 0.000 description 2
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 2
- 239000002671 adjuvant Substances 0.000 description 2
- 229960001631 carbomer Drugs 0.000 description 2
- 229910000420 cerium oxide Inorganic materials 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 239000006071 cream Substances 0.000 description 2
- ZAKOWWREFLAJOT-UHFFFAOYSA-N d-alpha-Tocopheryl acetate Natural products CC(=O)OC1=C(C)C(C)=C2OC(CCCC(C)CCCC(C)CCCC(C)C)(C)CCC2=C1C ZAKOWWREFLAJOT-UHFFFAOYSA-N 0.000 description 2
- 235000014113 dietary fatty acids Nutrition 0.000 description 2
- 229940120503 dihydroxyacetone Drugs 0.000 description 2
- 229940008099 dimethicone Drugs 0.000 description 2
- 239000004205 dimethyl polysiloxane Substances 0.000 description 2
- 235000013870 dimethyl polysiloxane Nutrition 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 210000002615 epidermis Anatomy 0.000 description 2
- 239000000194 fatty acid Substances 0.000 description 2
- 229930195729 fatty acid Natural products 0.000 description 2
- 238000009472 formulation Methods 0.000 description 2
- FOYKKGHVWRFIBD-UHFFFAOYSA-N gamma-tocopherol acetate Natural products CC(=O)OC1=C(C)C(C)=C2OC(CCCC(C)CCCC(C)CCCC(C)C)(C)CCC2=C1 FOYKKGHVWRFIBD-UHFFFAOYSA-N 0.000 description 2
- 239000000499 gel Substances 0.000 description 2
- BXWNKGSJHAJOGX-UHFFFAOYSA-N hexadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCO BXWNKGSJHAJOGX-UHFFFAOYSA-N 0.000 description 2
- 229910052500 inorganic mineral Inorganic materials 0.000 description 2
- 235000010270 methyl p-hydroxybenzoate Nutrition 0.000 description 2
- 239000004292 methyl p-hydroxybenzoate Substances 0.000 description 2
- 229960002216 methylparaben Drugs 0.000 description 2
- 239000011707 mineral Substances 0.000 description 2
- DNIAPMSPPWPWGF-UHFFFAOYSA-N monopropylene glycol Natural products CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 2
- 239000003960 organic solvent Substances 0.000 description 2
- BMMGVYCKOGBVEV-UHFFFAOYSA-N oxo(oxoceriooxy)cerium Chemical compound [Ce]=O.O=[Ce]=O BMMGVYCKOGBVEV-UHFFFAOYSA-N 0.000 description 2
- 229960001173 oxybenzone Drugs 0.000 description 2
- 229960005323 phenoxyethanol Drugs 0.000 description 2
- 229920000435 poly(dimethylsiloxane) Polymers 0.000 description 2
- 235000010232 propyl p-hydroxybenzoate Nutrition 0.000 description 2
- 239000004405 propyl p-hydroxybenzoate Substances 0.000 description 2
- 229960003415 propylparaben Drugs 0.000 description 2
- 230000003381 solubilizing effect Effects 0.000 description 2
- 230000000475 sunscreen effect Effects 0.000 description 2
- 239000000516 sunscreening agent Substances 0.000 description 2
- 239000002562 thickening agent Substances 0.000 description 2
- 235000013311 vegetables Nutrition 0.000 description 2
- FIDRAVVQGKNYQK-UHFFFAOYSA-N 1,2,3,4-tetrahydrotriazine Chemical compound C1NNNC=C1 FIDRAVVQGKNYQK-UHFFFAOYSA-N 0.000 description 1
- VBICKXHEKHSIBG-UHFFFAOYSA-N 1-monostearoylglycerol Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC(O)CO VBICKXHEKHSIBG-UHFFFAOYSA-N 0.000 description 1
- ABEXEQSGABRUHS-UHFFFAOYSA-N 16-methylheptadecyl 16-methylheptadecanoate Chemical compound CC(C)CCCCCCCCCCCCCCCOC(=O)CCCCCCCCCCCCCCC(C)C ABEXEQSGABRUHS-UHFFFAOYSA-N 0.000 description 1
- MEINCZCLWIPDPV-UHFFFAOYSA-N 2-[bis(2-hydroxyethyl)amino]ethanol;4-phenyl-1h-benzimidazole-2-sulfonic acid Chemical compound OCCN(CCO)CCO.C1=CC=C2NC(S(=O)(=O)O)=NC2=C1C1=CC=CC=C1 MEINCZCLWIPDPV-UHFFFAOYSA-N 0.000 description 1
- TYYHDKOVFSVWON-UHFFFAOYSA-N 2-butyl-2-methoxy-1,3-diphenylpropane-1,3-dione Chemical compound C=1C=CC=CC=1C(=O)C(OC)(CCCC)C(=O)C1=CC=CC=C1 TYYHDKOVFSVWON-UHFFFAOYSA-N 0.000 description 1
- JGUMTYWKIBJSTN-UHFFFAOYSA-N 2-ethylhexyl 4-[[4,6-bis[4-(2-ethylhexoxycarbonyl)anilino]-1,3,5-triazin-2-yl]amino]benzoate Chemical compound C1=CC(C(=O)OCC(CC)CCCC)=CC=C1NC1=NC(NC=2C=CC(=CC=2)C(=O)OCC(CC)CCCC)=NC(NC=2C=CC(=CC=2)C(=O)OCC(CC)CCCC)=N1 JGUMTYWKIBJSTN-UHFFFAOYSA-N 0.000 description 1
- QCDWFXQBSFUVSP-UHFFFAOYSA-N 2-phenoxyethanol Chemical compound OCCOC1=CC=CC=C1 QCDWFXQBSFUVSP-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N Acrylic acid Chemical compound OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- 244000007835 Cyamopsis tetragonoloba Species 0.000 description 1
- SNPLKNRPJHDVJA-ZETCQYMHSA-N D-panthenol Chemical compound OCC(C)(C)[C@@H](O)C(=O)NCCCO SNPLKNRPJHDVJA-ZETCQYMHSA-N 0.000 description 1
- 239000003109 Disodium ethylene diamine tetraacetate Substances 0.000 description 1
- 206010015150 Erythema Diseases 0.000 description 1
- 229920001479 Hydroxyethyl methyl cellulose Polymers 0.000 description 1
- 206010020751 Hypersensitivity Diseases 0.000 description 1
- 239000004909 Moisturizer Substances 0.000 description 1
- CAHKINHBCWCHCF-UHFFFAOYSA-N N-acetyltyrosine Chemical compound CC(=O)NC(C(O)=O)CC1=CC=C(O)C=C1 CAHKINHBCWCHCF-UHFFFAOYSA-N 0.000 description 1
- 239000005662 Paraffin oil Substances 0.000 description 1
- 206010063493 Premature ageing Diseases 0.000 description 1
- 208000032038 Premature aging Diseases 0.000 description 1
- 239000007983 Tris buffer Substances 0.000 description 1
- IOJXOCNVUFGVDG-UHFFFAOYSA-M [OH-].[K+].C1(=CC=CC=C1)C1=CC=CC=2N=C(NC=21)S(=O)(=O)O Chemical compound [OH-].[K+].C1(=CC=CC=C1)C1=CC=CC=2N=C(NC=21)S(=O)(=O)O IOJXOCNVUFGVDG-UHFFFAOYSA-M 0.000 description 1
- 239000002535 acidifier Substances 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 150000001336 alkenes Chemical class 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- CEGOLXSVJUTHNZ-UHFFFAOYSA-K aluminium tristearate Chemical compound [Al+3].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O CEGOLXSVJUTHNZ-UHFFFAOYSA-K 0.000 description 1
- 229940063655 aluminum stearate Drugs 0.000 description 1
- 125000002490 anilino group Chemical group [H]N(*)C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 239000008346 aqueous phase Substances 0.000 description 1
- 229960005193 avobenzone Drugs 0.000 description 1
- 239000002610 basifying agent Substances 0.000 description 1
- 150000001277 beta hydroxy acids Chemical class 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 235000010980 cellulose Nutrition 0.000 description 1
- 229960000541 cetyl alcohol Drugs 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 230000018109 developmental process Effects 0.000 description 1
- XXJWXESWEXIICW-UHFFFAOYSA-N diethylene glycol monoethyl ether Chemical compound CCOCCOCCO XXJWXESWEXIICW-UHFFFAOYSA-N 0.000 description 1
- 235000019301 disodium ethylene diamine tetraacetate Nutrition 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- XJFGDLJQUJQUEI-UHFFFAOYSA-N dodecyl decanoate dodecyl octanoate Chemical compound CCCCCCCCCCCCOC(=O)CCCCCCC.CCCCCCCCCCCCOC(=O)CCCCCCCCC XJFGDLJQUJQUEI-UHFFFAOYSA-N 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 239000003974 emollient agent Substances 0.000 description 1
- HEOCBCNFKCOKBX-SDNWHVSQSA-N enzacamene Chemical compound C1=CC(C)=CC=C1\C=C/1C(=O)C2(C)CCC\1C2(C)C HEOCBCNFKCOKBX-SDNWHVSQSA-N 0.000 description 1
- 231100000321 erythema Toxicity 0.000 description 1
- 210000004709 eyebrow Anatomy 0.000 description 1
- 210000000720 eyelash Anatomy 0.000 description 1
- 239000003925 fat Substances 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 150000002191 fatty alcohols Chemical class 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 239000006260 foam Substances 0.000 description 1
- 239000003205 fragrance Substances 0.000 description 1
- 235000011187 glycerol Nutrition 0.000 description 1
- 229940074046 glyceryl laurate Drugs 0.000 description 1
- 229940075529 glyceryl stearate Drugs 0.000 description 1
- 229920013818 hydroxypropyl guar gum Polymers 0.000 description 1
- 239000001866 hydroxypropyl methyl cellulose Substances 0.000 description 1
- UFVKGYZPFZQRLF-UHFFFAOYSA-N hydroxypropyl methyl cellulose Chemical compound OC1C(O)C(OC)OC(CO)C1OC1C(O)C(O)C(OC2C(C(O)C(OC3C(C(O)C(O)C(CO)O3)O)C(CO)O2)O)C(CO)O1 UFVKGYZPFZQRLF-UHFFFAOYSA-N 0.000 description 1
- 235000010979 hydroxypropyl methyl cellulose Nutrition 0.000 description 1
- 229920003088 hydroxypropyl methyl cellulose Polymers 0.000 description 1
- 230000001939 inductive effect Effects 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 229940060384 isostearyl isostearate Drugs 0.000 description 1
- 239000004922 lacquer Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000006210 lotion Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 235000013336 milk Nutrition 0.000 description 1
- 239000008267 milk Substances 0.000 description 1
- 210000004080 milk Anatomy 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 235000010446 mineral oil Nutrition 0.000 description 1
- 230000001333 moisturizer Effects 0.000 description 1
- VAMFXQBUQXONLZ-UHFFFAOYSA-N n-alpha-eicosene Natural products CCCCCCCCCCCCCCCCCCC=C VAMFXQBUQXONLZ-UHFFFAOYSA-N 0.000 description 1
- WWZKQHOCKIZLMA-UHFFFAOYSA-N octanoic acid Chemical compound CCCCCCCC(O)=O WWZKQHOCKIZLMA-UHFFFAOYSA-N 0.000 description 1
- IIGMITQLXAGZTL-UHFFFAOYSA-N octyl octadecanoate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCCCCCCCC IIGMITQLXAGZTL-UHFFFAOYSA-N 0.000 description 1
- 239000003605 opacifier Substances 0.000 description 1
- 229940101267 panthenol Drugs 0.000 description 1
- 235000020957 pantothenol Nutrition 0.000 description 1
- 239000011619 pantothenol Substances 0.000 description 1
- 235000011837 pasties Nutrition 0.000 description 1
- 235000019271 petrolatum Nutrition 0.000 description 1
- 231100000760 phototoxic Toxicity 0.000 description 1
- 229940048845 polyglyceryl-3 diisostearate Drugs 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 229920005862 polyol Polymers 0.000 description 1
- 150000003077 polyols Chemical class 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- RMGVATURDVPNOZ-UHFFFAOYSA-M potassium;hexadecyl hydrogen phosphate Chemical compound [K+].CCCCCCCCCCCCCCCCOP(O)([O-])=O RMGVATURDVPNOZ-UHFFFAOYSA-M 0.000 description 1
- UEJWQQOFBFKFTB-UHFFFAOYSA-M potassium;propane-1,2-diol;hydroxide Chemical compound [OH-].[K+].CC(O)CO UEJWQQOFBFKFTB-UHFFFAOYSA-M 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- 239000011164 primary particle Substances 0.000 description 1
- 239000003380 propellant Substances 0.000 description 1
- WCQDGRGDJWBPJX-UHFFFAOYSA-N propyl 4-hydroxybenzoate;sodium Chemical compound [Na].[Na].CCCOC(=O)C1=CC=C(O)C=C1 WCQDGRGDJWBPJX-UHFFFAOYSA-N 0.000 description 1
- 238000012216 screening Methods 0.000 description 1
- 230000037307 sensitive skin Effects 0.000 description 1
- 239000003352 sequestering agent Substances 0.000 description 1
- 239000002453 shampoo Substances 0.000 description 1
- 229920002545 silicone oil Polymers 0.000 description 1
- 231100000075 skin burn Toxicity 0.000 description 1
- 230000037380 skin damage Effects 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 230000000699 topical effect Effects 0.000 description 1
- LADGBHLMCUINGV-UHFFFAOYSA-N tricaprin Chemical compound CCCCCCCCCC(=O)OCC(OC(=O)CCCCCCCCC)COC(=O)CCCCCCCCC LADGBHLMCUINGV-UHFFFAOYSA-N 0.000 description 1
- UUJLHYCIMQOUKC-UHFFFAOYSA-N trimethyl-[oxo(trimethylsilylperoxy)silyl]peroxysilane Chemical compound C[Si](C)(C)OO[Si](=O)OO[Si](C)(C)C UUJLHYCIMQOUKC-UHFFFAOYSA-N 0.000 description 1
- 125000001493 tyrosinyl group Chemical class [H]OC1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])C([H])(N([H])[H])C(*)=O 0.000 description 1
- 229940088594 vitamin Drugs 0.000 description 1
- 239000011782 vitamin Substances 0.000 description 1
- 235000013343 vitamin Nutrition 0.000 description 1
- 229930003231 vitamin Natural products 0.000 description 1
- 239000007762 w/o emulsion Substances 0.000 description 1
- 230000037303 wrinkles Effects 0.000 description 1
- 239000000230 xanthan gum Substances 0.000 description 1
- 229920001285 xanthan gum Polymers 0.000 description 1
- 235000010493 xanthan gum Nutrition 0.000 description 1
- 229940082509 xanthan gum Drugs 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/33—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
- A61K8/37—Esters of carboxylic acids
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/33—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
- A61K8/35—Ketones, e.g. benzophenone
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/49—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds
- A61K8/494—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds with more than one nitrogen as the only hetero atom
- A61K8/4966—Triazines or their condensed derivatives
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q17/00—Barrier preparations; Preparations brought into direct contact with the skin for affording protection against external influences, e.g. sunlight, X-rays or other harmful rays, corrosive materials, bacteria or insect stings
- A61Q17/04—Topical preparations for affording protection against sunlight or other radiation; Topical sun tanning preparations
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Birds (AREA)
- Epidemiology (AREA)
- Emergency Medicine (AREA)
- Dermatology (AREA)
- Cosmetics (AREA)
Abstract
Description
Claims (1)
- 8 REVENDICATIONS1. Base cosmétique comprenant au moins un premier filtre des rayonnements UV-A et/ou UV-B, lipophile, solide et un agent solubilisant le 2-5 éthylhexyl-p-méthoxycinnamate et un agent photoprotecteur.2. Composition selon la revendication 1 caractérisée en ce que l'agent photoprotecteur est choisi parmi les pigments et les nanopigments d'oxydes métalliques, éventuellement enrobés, capables de bloquer physiquement, par diffusion et/ou réflexion, le rayonnement UV.3. Composition selon l'une quelconque des revendications précédentes,, caractérisée en ce que les pigments et/ou les nanopigments sont choisis parmi les oxydes de titane, les oxydes de zinc, les oxydes de fer, les oxydes de zirconium, les oxydes de cérium et les mélanges de ceux-ci.4. Composition cosmétique comprenant une base cosmétique selon les revendications 1 ou 2 et un support cosmétiquement acceptable.5. Composition selon l'une quelconque des revendications précédentes, caractérisée en ce que le premier filtre des rayonnements UV-A et/ou UV-B, lipophile, solide est choisi parmi la 2,4,6-tris-[p-(2'-éthylhexyl-l'oxycarbonyl)-anilino]-1,3,5-triazine, le 4-(t-butyl)-4'-méthoxy-dibenzoylméthane, la 2-hydroxy-4-méthoxy-benzophénone et le 3-(4'méthylbenzylidène)-camphre.6. Composition selon l'une quelconque des revendications précédentes,, caractérisée en ce que le premier filtre des rayonnements UV-A et/ou UV-B, lipophile, solide est présent en une proportion allant de 0,5 à 10 0/0 en poids par rapport au poids total de la composition.7. Composition selon l'une quelconque des revendications précédentes, caractérisée en ce que le 2-éthylhexyl-p-méthoxycinnamate est présent en une proportion allant de 0,5 à :30 % en poids par rapport au poids total de la composition, de préférence de 1 à 10 %.8. Composition selon selon l'une quelconque des revendications précédentes,caractérisée en ce que l'agent photoprotecteur est présent en une proportion allant de 0,5 à 30 % en poids par rapport au poids total de la composition, de préférence de 1 à 8 %.9. Composition selon l'une quelconque des revendications 35 précédentes, caractérisée en ce que le support cosmétiquement acceptable se présente sous la forme d'une émulsion de type huile-dans-eau ou eau-danshuile.10. Composition selon l'une quelconque des revendications 2 à 7, caractérisée en ce qu'elle comprend en outre au moins un second filtre choisi parmi les filtres organiques, actifs dans l'UV-A et/ou l'UV-B, hydrophiles ou lipophiles.11. Composition selon la revendication 10, caractérisée en ce que le second filtre est choisi parmi les dérivés salicyliques, les dérivés du camphre, les dérivés de la triazine, les dérivés de la benzophénone, les lo dérivés du dibenzoylméthane, les dérivés de p,f3-diphénylacrylate, les dérivés de l'acide p-aminobenzoïque et les mélanges de ceux-ci.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR0502362A FR2882927B1 (fr) | 2005-03-09 | 2005-03-09 | Compositions cosmetiques solaires |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR0502362A FR2882927B1 (fr) | 2005-03-09 | 2005-03-09 | Compositions cosmetiques solaires |
Publications (2)
Publication Number | Publication Date |
---|---|
FR2882927A1 true FR2882927A1 (fr) | 2006-09-15 |
FR2882927B1 FR2882927B1 (fr) | 2009-07-03 |
Family
ID=35429523
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
FR0502362A Active FR2882927B1 (fr) | 2005-03-09 | 2005-03-09 | Compositions cosmetiques solaires |
Country Status (1)
Country | Link |
---|---|
FR (1) | FR2882927B1 (fr) |
Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5827508A (en) * | 1996-09-27 | 1998-10-27 | The Procter & Gamble Company | Stable photoprotective compositions |
FR2779959A1 (fr) * | 1998-06-18 | 1999-12-24 | Oreal | Compositions cosmetiques photoprotectrices contenant un benzazole n-substitue, un derive d'acide cinnamique et un filtre organique uv-a hydrosoluble |
FR2795318A1 (fr) * | 1999-06-25 | 2000-12-29 | Jean Noel Thorel | Procede de photostabilisation du 4-(ter.butyl) 4'-methoxy dibenzoylmethane et compositions filtrantes anti-solaires |
US6280712B1 (en) * | 1997-08-29 | 2001-08-28 | Cognis Deutschland Gmbh | Sun screen agents |
WO2002017874A1 (fr) * | 2000-08-29 | 2002-03-07 | Ciba Specialty Chemicals Holding Inc. | Compositions antisolaires contenant des derives triazine et des derives triazole |
-
2005
- 2005-03-09 FR FR0502362A patent/FR2882927B1/fr active Active
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5827508A (en) * | 1996-09-27 | 1998-10-27 | The Procter & Gamble Company | Stable photoprotective compositions |
US6280712B1 (en) * | 1997-08-29 | 2001-08-28 | Cognis Deutschland Gmbh | Sun screen agents |
FR2779959A1 (fr) * | 1998-06-18 | 1999-12-24 | Oreal | Compositions cosmetiques photoprotectrices contenant un benzazole n-substitue, un derive d'acide cinnamique et un filtre organique uv-a hydrosoluble |
FR2795318A1 (fr) * | 1999-06-25 | 2000-12-29 | Jean Noel Thorel | Procede de photostabilisation du 4-(ter.butyl) 4'-methoxy dibenzoylmethane et compositions filtrantes anti-solaires |
WO2002017874A1 (fr) * | 2000-08-29 | 2002-03-07 | Ciba Specialty Chemicals Holding Inc. | Compositions antisolaires contenant des derives triazine et des derives triazole |
Also Published As
Publication number | Publication date |
---|---|
FR2882927B1 (fr) | 2009-07-03 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
EP0685222B2 (fr) | Compositions cosmétiques photoprotectrices et utilisations | |
EP0685225B1 (fr) | Compositions cosmétiques antisolaires et utilisations | |
EP0689828B2 (fr) | Compositions cosmétiques antisolaires comprenant de la 2,4,6-tris(p-(2'-éthylhexyl-1'-oxycarbonyl)anilino)-1,3,5-triazine et du malate de dioctyle et utilisations | |
EP0685223B1 (fr) | Compositions cosmétiques anti-UV et utilisations | |
CA2150772C (fr) | Compositions cosmetiques photoprotectrices a base d'un melange synergetique de filtres et de nanopigments et utilisations | |
FR2758982A1 (fr) | Emulsions eau-dans-huile a base de deux emulsionnants particuliers et apllications cosmetiques | |
FR2720632A1 (fr) | Compositions cosmétiques photoprotectrices contenant un système filtrant les rayons UV et des polymères particuliers et utilisations. | |
CA2150774C (fr) | Compositions cosmetiques photoprotectrices a base d'un melange synergetique de filtres et utilisations | |
WO1995000111A1 (fr) | Compositions cosmetiques filtrantes contenant un agent hydrophile comportant au moins un radical acide sulfonique | |
EP1002523B1 (fr) | Compositions cosmétiques photoprotectrices | |
FR2800991A1 (fr) | Procede de photostabilisation de butylmethoxydibenzoylmethane et utilisation dans des compositions cosmetiques anti-solaires | |
EP0860165B1 (fr) | Compositions cosmétiques pour la photoprotection de la peau et/ou des cheveux à base d'un mélange synergique de filtres | |
EP0865271B2 (fr) | Utilisation de l' alpha-cyano-béta, béta-diphénylacrylate de 2-éthylhexyle en vue d' améliorer la stabilité à la lumière du p-méthyl benzylidène camphre | |
EP0766959B1 (fr) | Compositions cosmétique photoprotectrices contenant des nanopigments de Tio2 et un acylaminoacide | |
FR2768337A1 (fr) | Emulsions triples du type e/h/e contenant un systeme photoprotecteur capable de filtrer les rayons uv; leurs utilisations en cosmetique | |
EP0813857A1 (fr) | Nouveau procédé de préparation de compositions uv-filtrantes, compositions susceptibles d'être obtenues par ce procédé et applications | |
FR2765104A1 (fr) | Compositions cosmetiques et utilisations pour la protection contres les rayonnements uv-a et uv-b | |
EP0835094B1 (fr) | Compositions cosmetiques filtrantes contenant un dibenzoylmethane, un beta'-diphenylacrylate d'alkyle et une silicone benzotriazole | |
FR2795319A1 (fr) | Procede de photostabilisation du 4-(ter.butyl) 4'-methoxy dibenzoylmethane et compositions filtrantes anti-solaires | |
FR2882927A1 (fr) | Compositions cosmetiques solaires | |
EP1150649B1 (fr) | Compositions cosmetiques pour la photoprotection de la peau et/ou des cheveux contenant un derive silicone de benzotriazole et une bis-resorcinyl triazine | |
FR2768730A1 (fr) | Procede de photostabilisation du 4-(ter.butyl) 4'-methoxy dibenzoylmethane, compositions filtrantes ainsi obtenues et leurs utilisations | |
FR2795318A1 (fr) | Procede de photostabilisation du 4-(ter.butyl) 4'-methoxy dibenzoylmethane et compositions filtrantes anti-solaires | |
FR2779956A1 (fr) | Compositions cosmetiques photoprotectrices contenant un benzazole n-substitue, un derive de dibenzoylmethane et un filtre organique uv-b liquide | |
FR2774586A3 (fr) | Compositions cosmetiques photoprotectrices contenant une association de filtres avec un emulsionnant naturel |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
PLFP | Fee payment |
Year of fee payment: 12 |
|
PLFP | Fee payment |
Year of fee payment: 13 |
|
PLFP | Fee payment |
Year of fee payment: 14 |
|
PLFP | Fee payment |
Year of fee payment: 16 |
|
PLFP | Fee payment |
Year of fee payment: 17 |
|
PLFP | Fee payment |
Year of fee payment: 18 |
|
PLFP | Fee payment |
Year of fee payment: 19 |
|
AU | Other action affecting the ownership or exploitation of an industrial property right |
Effective date: 20231016 |
|
CL | Concession to grant licences |
Name of requester: NAOS, FR Effective date: 20231016 Name of requester: NAOS INSTITUTE OF LIFE SCIENCE, FR Effective date: 20231016 |
|
PLFP | Fee payment |
Year of fee payment: 20 |