JP4154084B2 - ４，４−ジアリールブタジエンのｕｖフィルター、サンスクリーン含有化粧品及び製剤としての使用、４，４−ジアリールブタジエン及び製剤 - Google Patents
４，４−ジアリールブタジエンのｕｖフィルター、サンスクリーン含有化粧品及び製剤としての使用、４，４−ジアリールブタジエン及び製剤 Download PDFInfo
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- JP4154084B2 JP4154084B2 JP18225499A JP18225499A JP4154084B2 JP 4154084 B2 JP4154084 B2 JP 4154084B2 JP 18225499 A JP18225499 A JP 18225499A JP 18225499 A JP18225499 A JP 18225499A JP 4154084 B2 JP4154084 B2 JP 4154084B2
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- Prior art keywords
- alkylene
- hydrogen
- alkyl
- formula
- formulations
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- 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.)
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- 239000000203 mixture Substances 0.000 title claims abstract description 34
- 239000002537 cosmetic Substances 0.000 title claims description 28
- 239000000516 sunscreening agent Substances 0.000 title claims description 25
- 230000000475 sunscreen effect Effects 0.000 title claims description 20
- 238000009472 formulation Methods 0.000 title claims description 19
- 239000004904 UV filter Substances 0.000 title claims description 8
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 38
- 150000001993 dienes Chemical class 0.000 claims abstract description 9
- 150000001875 compounds Chemical class 0.000 claims description 40
- 239000001257 hydrogen Substances 0.000 claims description 37
- 150000002431 hydrogen Chemical class 0.000 claims description 26
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 9
- 210000003491 skin Anatomy 0.000 claims description 8
- 238000010521 absorption reaction Methods 0.000 claims description 3
- 210000002615 epidermis Anatomy 0.000 claims description 3
- 238000002360 preparation method Methods 0.000 claims description 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 2
- 125000003161 (C1-C6) alkylene group Chemical group 0.000 claims 1
- 239000012963 UV stabilizer Substances 0.000 claims 1
- 239000000825 pharmaceutical preparation Substances 0.000 claims 1
- 125000001424 substituent group Chemical group 0.000 abstract description 10
- 229910052794 bromium Inorganic materials 0.000 abstract description 9
- 229910052801 chlorine Inorganic materials 0.000 abstract description 9
- 125000003118 aryl group Chemical group 0.000 abstract description 8
- 125000000217 alkyl group Chemical group 0.000 abstract description 7
- 229910052740 iodine Inorganic materials 0.000 abstract description 7
- 125000003342 alkenyl group Chemical group 0.000 abstract description 6
- QGZKDVFQNNGYKY-UHFFFAOYSA-O ammonium group Chemical group [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 abstract description 6
- 229910052760 oxygen Inorganic materials 0.000 abstract description 6
- 150000007942 carboxylates Chemical class 0.000 abstract description 5
- 125000001072 heteroaryl group Chemical group 0.000 abstract description 5
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 abstract description 5
- 125000002252 acyl group Chemical group 0.000 abstract description 3
- 125000000392 cycloalkenyl group Chemical group 0.000 abstract description 3
- 125000000753 cycloalkyl group Chemical group 0.000 abstract description 3
- 101100134922 Gallus gallus COR5 gene Proteins 0.000 abstract 1
- 101100134925 Gallus gallus COR6 gene Proteins 0.000 abstract 1
- -1 diphenyl acrylate Chemical compound 0.000 description 68
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 26
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 19
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 18
- DNIAPMSPPWPWGF-UHFFFAOYSA-N propylene glycol Substances CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 16
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 15
- HQKMJHAJHXVSDF-UHFFFAOYSA-L magnesium stearate Chemical compound [Mg+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O HQKMJHAJHXVSDF-UHFFFAOYSA-L 0.000 description 14
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 12
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 10
- 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 description 10
- 239000004359 castor oil Substances 0.000 description 10
- 235000019438 castor oil Nutrition 0.000 description 10
- LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 10
- ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 10
- 229960001679 octinoxate Drugs 0.000 description 10
- 239000000126 substance Substances 0.000 description 10
- 238000006243 chemical reaction Methods 0.000 description 9
- 229920001577 copolymer Polymers 0.000 description 9
- 239000004408 titanium dioxide Substances 0.000 description 9
- HEOCBCNFKCOKBX-RELGSGGGSA-N (1s,2e,4r)-4,7,7-trimethyl-2-[(4-methylphenyl)methylidene]bicyclo[2.2.1]heptan-3-one Chemical compound C1=CC(C)=CC=C1\C=C/1C(=O)[C@]2(C)CC[C@H]\1C2(C)C HEOCBCNFKCOKBX-RELGSGGGSA-N 0.000 description 8
- 239000000460 chlorine Substances 0.000 description 8
- 229960004697 enzacamene Drugs 0.000 description 8
- 229940119170 jojoba wax Drugs 0.000 description 8
- LXCFILQKKLGQFO-UHFFFAOYSA-N methylparaben Chemical compound COC(=O)C1=CC=C(O)C=C1 LXCFILQKKLGQFO-UHFFFAOYSA-N 0.000 description 8
- QELSKZZBTMNZEB-UHFFFAOYSA-N propylparaben Chemical compound CCCOC(=O)C1=CC=C(O)C=C1 QELSKZZBTMNZEB-UHFFFAOYSA-N 0.000 description 8
- 125000004432 carbon atom Chemical group C* 0.000 description 7
- 229940125904 compound 1 Drugs 0.000 description 7
- BEPAFCGSDWSTEL-UHFFFAOYSA-N dimethyl malonate Chemical compound COC(=O)CC(=O)OC BEPAFCGSDWSTEL-UHFFFAOYSA-N 0.000 description 7
- 239000000839 emulsion Substances 0.000 description 7
- 235000019359 magnesium stearate Nutrition 0.000 description 7
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 7
- 230000005855 radiation Effects 0.000 description 7
- 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 6
- KCXVZYZYPLLWCC-UHFFFAOYSA-N EDTA Chemical compound OC(=O)CN(CC(O)=O)CCN(CC(O)=O)CC(O)=O KCXVZYZYPLLWCC-UHFFFAOYSA-N 0.000 description 6
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 6
- 125000003545 alkoxy group Chemical group 0.000 description 6
- 239000003054 catalyst Substances 0.000 description 6
- 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 6
- 150000002148 esters Chemical class 0.000 description 6
- 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 6
- 239000000499 gel Substances 0.000 description 6
- XUGNVMKQXJXZCD-UHFFFAOYSA-N isopropyl palmitate Chemical compound CCCCCCCCCCCCCCCC(=O)OC(C)C XUGNVMKQXJXZCD-UHFFFAOYSA-N 0.000 description 6
- 239000002480 mineral oil Substances 0.000 description 6
- 235000010446 mineral oil Nutrition 0.000 description 6
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 6
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 6
- 125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 6
- 239000002904 solvent Substances 0.000 description 6
- 239000008346 aqueous phase Substances 0.000 description 5
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 5
- 239000003205 fragrance Substances 0.000 description 5
- 239000011521 glass Substances 0.000 description 5
- 125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 5
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 5
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 5
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 5
- 235000019341 magnesium sulphate Nutrition 0.000 description 5
- 239000000178 monomer Substances 0.000 description 5
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 5
- 239000003921 oil Substances 0.000 description 5
- 239000000243 solution Substances 0.000 description 5
- LADGBHLMCUINGV-UHFFFAOYSA-N tricaprin Chemical compound CCCCCCCCCC(=O)OCC(OC(=O)CCCCCCCCC)COC(=O)CCCCCCCCC LADGBHLMCUINGV-UHFFFAOYSA-N 0.000 description 5
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 4
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical group N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
- 239000003109 Disodium ethylene diamine tetraacetate Substances 0.000 description 4
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 4
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 4
- NQRYJNQNLNOLGT-UHFFFAOYSA-N Piperidine Chemical compound C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 description 4
- 239000006071 cream Substances 0.000 description 4
- 125000004663 dialkyl amino group Chemical group 0.000 description 4
- 235000014113 dietary fatty acids Nutrition 0.000 description 4
- 229940008099 dimethicone Drugs 0.000 description 4
- 239000004205 dimethyl polysiloxane Substances 0.000 description 4
- 235000013870 dimethyl polysiloxane Nutrition 0.000 description 4
- 235000019301 disodium ethylene diamine tetraacetate Nutrition 0.000 description 4
- 239000000194 fatty acid Substances 0.000 description 4
- 229930195729 fatty acid Natural products 0.000 description 4
- 150000004665 fatty acids Chemical class 0.000 description 4
- ZCTXEAQXZGPWFG-UHFFFAOYSA-N imidurea Chemical compound O=C1NC(=O)N(CO)C1NC(=O)NCNC(=O)NC1C(=O)NC(=O)N1CO ZCTXEAQXZGPWFG-UHFFFAOYSA-N 0.000 description 4
- 239000006210 lotion Substances 0.000 description 4
- 239000004292 methyl p-hydroxybenzoate Substances 0.000 description 4
- 235000010270 methyl p-hydroxybenzoate Nutrition 0.000 description 4
- 229960002216 methylparaben Drugs 0.000 description 4
- 125000000740 n-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 4
- 125000001971 neopentyl group Chemical group [H]C([*])([H])C(C([H])([H])[H])(C([H])([H])[H])C([H])([H])[H] 0.000 description 4
- 229940060184 oil ingredients Drugs 0.000 description 4
- 239000008194 pharmaceutical composition Substances 0.000 description 4
- 229920000435 poly(dimethylsiloxane) Polymers 0.000 description 4
- 239000004405 propyl p-hydroxybenzoate Substances 0.000 description 4
- 235000010232 propyl p-hydroxybenzoate Nutrition 0.000 description 4
- 229960003415 propylparaben Drugs 0.000 description 4
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 4
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 4
- 125000001973 tert-pentyl group Chemical group [H]C([H])([H])C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 4
- 239000001993 wax Substances 0.000 description 4
- 239000008096 xylene Substances 0.000 description 4
- VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical group CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 description 3
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- 239000004354 Hydroxyethyl cellulose Substances 0.000 description 3
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
- 125000002947 alkylene group Chemical class 0.000 description 3
- 239000002585 base Substances 0.000 description 3
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- 239000000975 dye Substances 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 3
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- 125000001972 isopentyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])C([H])([H])* 0.000 description 3
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- 150000003839 salts Chemical class 0.000 description 3
- 125000003548 sec-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 3
- 238000005809 transesterification reaction Methods 0.000 description 3
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- 125000005918 1,2-dimethylbutyl group Chemical group 0.000 description 2
- 125000004973 1-butenyl group Chemical group C(=CCC)* 0.000 description 2
- 125000006218 1-ethylbutyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C([H])([H])[H] 0.000 description 2
- 125000006039 1-hexenyl group Chemical group 0.000 description 2
- 125000004806 1-methylethylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 2
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- 125000004974 2-butenyl group Chemical group C(C=CC)* 0.000 description 2
- 125000006176 2-ethylbutyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(C([H])([H])*)C([H])([H])C([H])([H])[H] 0.000 description 2
- 125000006040 2-hexenyl group Chemical group 0.000 description 2
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- 125000006027 3-methyl-1-butenyl group Chemical group 0.000 description 2
- 125000003542 3-methylbutan-2-yl group Chemical group [H]C([H])([H])C([H])(*)C([H])(C([H])([H])[H])C([H])([H])[H] 0.000 description 2
- 125000005917 3-methylpentyl group Chemical group 0.000 description 2
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- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 2
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- 201000004624 Dermatitis Diseases 0.000 description 2
- ROSDSFDQCJNGOL-UHFFFAOYSA-N Dimethylamine Chemical compound CNC ROSDSFDQCJNGOL-UHFFFAOYSA-N 0.000 description 2
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- YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical compound C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 description 2
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- 208000000453 Skin Neoplasms Diseases 0.000 description 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 2
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- 229910052783 alkali metal Inorganic materials 0.000 description 2
- 125000005210 alkyl ammonium group Chemical group 0.000 description 2
- IYABWNGZIDDRAK-UHFFFAOYSA-N allene Chemical group C=C=C IYABWNGZIDDRAK-UHFFFAOYSA-N 0.000 description 2
- 230000007815 allergy Effects 0.000 description 2
- UBNYRXMKIIGMKK-RMKNXTFCSA-N amiloxate Chemical compound COC1=CC=C(\C=C\C(=O)OCCC(C)C)C=C1 UBNYRXMKIIGMKK-RMKNXTFCSA-N 0.000 description 2
- 230000000035 biogenic effect Effects 0.000 description 2
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 2
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- 230000006378 damage Effects 0.000 description 2
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- 150000002367 halogens Chemical class 0.000 description 2
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- 125000004491 isohexyl group Chemical group C(CCC(C)C)* 0.000 description 2
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- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 2
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- 125000001624 naphthyl group Chemical group 0.000 description 2
- 229910052757 nitrogen Inorganic materials 0.000 description 2
- 125000003538 pentan-3-yl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])C([H])([H])[H] 0.000 description 2
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- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 2
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Classifications
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- 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
- A61K8/46—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing sulfur
- A61K8/466—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing sulfur containing sulfonic acid derivatives; Salts
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- 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
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- 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
- A61K8/40—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing nitrogen
- A61K8/42—Amides
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
- A61P17/16—Emollients or protectives, e.g. against radiation
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- 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
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C233/00—Carboxylic acid amides
- C07C233/01—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms
- C07C233/34—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by amino groups
- C07C233/35—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by amino groups with the substituted hydrocarbon radical bound to the nitrogen atom of the carboxamide group by an acyclic carbon atom
- C07C233/40—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by amino groups with the substituted hydrocarbon radical bound to the nitrogen atom of the carboxamide group by an acyclic carbon atom having the carbon atom of the carboxamide group bound to an acyclic carbon atom of a carbon skeleton containing six-membered aromatic rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C309/00—Sulfonic acids; Halides, esters, or anhydrides thereof
- C07C309/01—Sulfonic acids
- C07C309/28—Sulfonic acids having sulfo groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton
- C07C309/57—Sulfonic acids having sulfo groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton containing carboxyl groups bound to the carbon skeleton
- C07C309/58—Carboxylic acid groups or esters thereof
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C309/00—Sulfonic acids; Halides, esters, or anhydrides thereof
- C07C309/01—Sulfonic acids
- C07C309/28—Sulfonic acids having sulfo groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton
- C07C309/57—Sulfonic acids having sulfo groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton containing carboxyl groups bound to the carbon skeleton
- C07C309/59—Nitrogen analogues of carboxyl groups
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C69/00—Esters of carboxylic acids; Esters of carbonic or haloformic acids
- C07C69/612—Esters of carboxylic acids having a carboxyl group bound to an acyclic carbon atom and having a six-membered aromatic ring in the acid moiety
- C07C69/618—Esters of carboxylic acids having a carboxyl group bound to an acyclic carbon atom and having a six-membered aromatic ring in the acid moiety having unsaturation outside the six-membered aromatic ring
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C69/00—Esters of carboxylic acids; Esters of carbonic or haloformic acids
- C07C69/66—Esters of carboxylic acids having esterified carboxylic groups bound to acyclic carbon atoms and having any of the groups OH, O—metal, —CHO, keto, ether, acyloxy, groups, groups, or in the acid moiety
- C07C69/73—Esters of carboxylic acids having esterified carboxylic groups bound to acyclic carbon atoms and having any of the groups OH, O—metal, —CHO, keto, ether, acyloxy, groups, groups, or in the acid moiety of unsaturated acids
- C07C69/738—Esters of keto-carboxylic acids or aldehydo-carboxylic acids
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K2800/00—Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
- A61K2800/40—Chemical, physico-chemical or functional or structural properties of particular ingredients
- A61K2800/52—Stabilizers
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- Organic Chemistry (AREA)
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Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19828463.2 | 1998-06-26 | ||
| DE19828463A DE19828463A1 (de) | 1998-06-26 | 1998-06-26 | 4,4-Diarylbutadiene als wasserlösliche photostabile UV-Filter für kosmetische und pharmazeutische Zubereitungen |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2000044452A JP2000044452A (ja) | 2000-02-15 |
| JP2000044452A5 JP2000044452A5 (enExample) | 2006-06-22 |
| JP4154084B2 true JP4154084B2 (ja) | 2008-09-24 |
Family
ID=7872072
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP18225499A Expired - Fee Related JP4154084B2 (ja) | 1998-06-26 | 1999-06-28 | ４，４−ジアリールブタジエンのｕｖフィルター、サンスクリーン含有化粧品及び製剤としての使用、４，４−ジアリールブタジエン及び製剤 |
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| Country | Link |
|---|---|
| US (2) | US6093385A (enExample) |
| EP (1) | EP0967200B1 (enExample) |
| JP (1) | JP4154084B2 (enExample) |
| CN (1) | CN1250207C (enExample) |
| AT (1) | ATE216694T1 (enExample) |
| AU (1) | AU757965B2 (enExample) |
| BR (1) | BR9902569A (enExample) |
| DE (2) | DE19828463A1 (enExample) |
| ES (1) | ES2177170T3 (enExample) |
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| WO2022136110A1 (fr) | 2020-12-23 | 2022-06-30 | L'oreal | Composition cosmétique comprenant des particules polymériques à base de fonctions acétoacétates |
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| FR3117854B1 (fr) | 2020-12-23 | 2024-03-15 | Oreal | Composition cosmétique comprenant des particules polymériques à base de fonctions acétoacétates |
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| FR3130596A1 (fr) | 2021-12-17 | 2023-06-23 | L'oreal | Composition cosmétique et/ou dermatologique comprenant au moins une mérocyanine et au moins de l’acide ascorbique et/ou l’un de ses dérivés |
| FR3130565B1 (fr) | 2021-12-20 | 2025-02-28 | Oreal | Utilisation de particules d’oxycarbonate de bismuth pour la filtration des rayonnements ultra-violets |
| FR3130606B1 (fr) | 2021-12-21 | 2025-10-24 | Oreal | Composition cosmétique comprenant un composé cellulosique particulaire, des particules d’aérogel de silice hydrophobe, et une cire d’origine végétale |
| FR3130608B1 (fr) | 2021-12-21 | 2023-11-24 | Oreal | Composition cosmétique comprenant un composé cellulosique particulaire, des particules d’aérogel de silice hydrophobe, un polymère semi-cristallin et une cire d’origine végétale |
| FR3130605B1 (fr) | 2021-12-21 | 2023-11-24 | Oreal | Composition cosmétique comprenant un composé cellulosique particulaire, des particules d’aérogel de silice hydrophobe, et un polymère semi-cristallin |
| FR3131529B1 (fr) | 2021-12-31 | 2025-04-18 | Oreal | Kit de personnalisation d’une composition cosmétique |
| FR3132637B1 (fr) | 2022-02-15 | 2025-05-02 | Oreal | Composition cosmétique ou dermatologique comprenant une mérocyanine et un complexe polyionique |
| FR3133311B1 (fr) | 2022-03-10 | 2025-12-12 | Oreal | Composition comprenant au moins un copolymere d’amps®, au moins un alkylpolyglucoside, au moins un filtre uv et du myristate d’isopropyle |
| EP4507659A1 (en) | 2022-04-15 | 2025-02-19 | L'oreal | Direct emulsion comprising a uv-screening agent, a lipophilic acrylic polymer, a fatty acid ester of a polyol and a carboxylic anionic surfactant |
| FR3134516B1 (fr) | 2022-04-15 | 2025-06-06 | Oreal | Emulsion directe comprenant un filtre UV, un polymère acrylique lipophile, un ester d’acide gras et de polyol et un dérivé d’acide aminé |
| FR3146591A1 (fr) | 2023-03-16 | 2024-09-20 | L'oreal | Emulsion directe comprenant un filtre UV, un polymère acrylique lipophile, un ester d’acide gras et de polyol et un tensioactif anionique carboxylique, de pH supérieur ou égal à 6 |
| EP4536176A1 (en) | 2022-06-10 | 2025-04-16 | L'oreal | Cosmetic sunscreen composition and use of a cosmetic sunscreen composition |
| FR3138306A1 (fr) | 2022-07-26 | 2024-02-02 | L'oreal | Composition comprenant un filtre UV, un polymère superabsorbant et un phospholipide |
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| FR3141061A1 (fr) | 2022-10-21 | 2024-04-26 | L'oreal | Composition comprenant un filtre organique lipophile, un filtre organique hydrophile, des particules sphériques de silice poreuse, des particules sphériques de cellulose, et une poudre d’acide aminé N-acylé |
| WO2024083567A1 (en) | 2022-10-21 | 2024-04-25 | L'oreal | Composition comprising a lipophilic organic screening agent, a hydrophilic organic screening agent, with an amount by weight of fatty phase between 20 and 70% |
| FR3141060A1 (fr) | 2022-10-21 | 2024-04-26 | L'oreal | Composition comprenant un filtre UV organique lipophile, un filtre UV organique hydrophile et un polymère gélifiant hydrophile spécifique |
| US20250325466A1 (en) | 2022-10-28 | 2025-10-23 | Dsm Ip Assets B.V. | Novel compositions |
| US20250325472A1 (en) | 2022-10-28 | 2025-10-23 | Dsm Ip Assets B.V. | Novel compositions |
| CN120112266A (zh) | 2022-10-28 | 2025-06-06 | 帝斯曼知识产权资产管理有限公司 | 包括人乳寡糖的防晒组合物 |
| EP4618948A1 (en) | 2022-11-18 | 2025-09-24 | L'oreal | Non-sticky stable composition with texture transformation property |
| FR3145093A1 (fr) | 2023-01-19 | 2024-07-26 | L'oreal | Composition stable non collante et non grasse avec propriété de transformation de texture |
| FR3142344A1 (fr) | 2022-11-30 | 2024-05-31 | L'oreal | Composition à base de rétinol |
| FR3142897A1 (fr) | 2022-12-09 | 2024-06-14 | L'oreal | Composition comprenant un filtre organique hydrodispersible et au moins un complexe polyionique contenant un polysaccharide cationique et un acide non polymérique ayant au moins 3 valeurs de pKa et/ou l’un de ses sels |
| WO2024124309A1 (en) | 2022-12-12 | 2024-06-20 | L'oreal | Cosmetic sunscreen composition and its use |
| WO2024124310A1 (en) | 2022-12-12 | 2024-06-20 | L'oreal | Cosmetic sunscreen composition and its use |
| FR3142898A1 (fr) | 2022-12-13 | 2024-06-14 | L'oreal | Procédé de traitement des matières kératiniques mettant en œuvre au moins un composé polysaccharide à fonctions acétoacétates |
| FR3142894A1 (fr) | 2022-12-13 | 2024-06-14 | L'oreal | Procédé de traitement des fibres kératiniques mettant en œuvre un composé issu de la condensation de poly(thi)ol, et d’acétoacétate, et un agent réticulant |
| FR3142893A1 (fr) | 2022-12-13 | 2024-06-14 | L'oreal | Procédé de traitement des matières kératiniques mettant en œuvre un composé issu de la condensation de poly(thi)ol et d’acétoacétate et un agent réticulant |
| FR3143344A1 (fr) | 2022-12-16 | 2024-06-21 | L'oreal | Composition comprenant un filtre UV, un polymère lipophile convenablement sélectionné, et un carraghénane |
| FR3143340B1 (fr) | 2022-12-20 | 2025-10-24 | Oreal | Kit de soin anti-âge pour les matières kératiniques |
| FR3144000A1 (fr) | 2022-12-27 | 2024-06-28 | L'oreal | Procédé de traitement des matières kératiniques mettant en œuvre au moins un (co)polymère d’alcool polyvinylique (PVA) à fonctions acétoacétates et au moins un agent réticulant |
| FR3144001A1 (fr) | 2022-12-27 | 2024-06-28 | L'oreal | Procédé de traitement des fibres kératiniques mettant en œuvre au moins un (co)polymère d’alcool polyvinylique (PVA) à fonctions acétoacétates |
| FR3143985A1 (fr) | 2022-12-27 | 2024-06-28 | L'oreal | Procédé de traitement des matières kératiniques mettant en œuvre au moins une huile à fonctions acétoacétates et au moins un agent réticulant |
| FR3143997A1 (fr) | 2022-12-27 | 2024-06-28 | L'oreal | Procédé de traitement des matières kératiniques mettant en œuvre au moins un composé alcoxysilane à fonctions acétoacétates et au moins un agent réticulant |
| FR3144134A1 (fr) | 2022-12-27 | 2024-06-28 | L'oreal | Procédé de traitement des fibres kératiniques mettant en œuvre au moins une huile à fonctions acétoacétates |
| FR3146067A1 (fr) | 2023-02-28 | 2024-08-30 | L'oreal | Composition cosmetique a base d'oxyde de zinc et de bisethyhexyloxyphenol methoxyphenyl triazine |
| FR3149779A1 (fr) | 2023-06-16 | 2024-12-20 | L'oreal | Composition comprenant un filtre UV, au moins 1 % en poids d’acide ascorbique et une gomme de scléroglucane |
| FR3149780A1 (fr) | 2023-06-16 | 2024-12-20 | L'oreal | Composition comprenant au moins 1 % en poids d’acide ascorbique, un filtre UV organique hydrosoluble et des filtres UV addditionnels |
| FR3149777A1 (fr) | 2023-06-16 | 2024-12-20 | L'oreal | Composition cosmétique ou dermatologique aqueuse comprenant une mérocyanine et un filtre UV hydrosoluble |
| FR3149778A1 (fr) | 2023-06-16 | 2024-12-20 | L'oreal | Composition comprenant au moins 1 % en poids d’acide ascorbique et un polymère lipophile convenablement sélectionné |
| FR3149786A1 (fr) | 2023-06-16 | 2024-12-20 | L'oreal | Composition comprenant un filtre UV, un polymère semi-cristallin contenant au moins une chaine d’alkyl acrylate et une gomme de scléroglucane |
| FR3150105A1 (fr) | 2023-06-22 | 2024-12-27 | L'oreal | Matériau composite d’oxycarbonate de bismuth et de composés organiques à groupe(s) carboxy pour la filtration des rayonnements ultra-violets |
| FR3150108A1 (fr) | 2023-06-22 | 2024-12-27 | L'oreal | Utilisation d’au moins une particule d’oxycarbonate de bismuth, et d’au moins un tensioactif pour la filtration des rayonnements ultra-violets |
| FR3150107A1 (fr) | 2023-06-22 | 2024-12-27 | L'oreal | Utilisation d’un matériau composite d’oxycarbonate de bismuth et de composés inorganiques pour la filtration des rayonnements ultra-violets |
| FR3150106A1 (fr) | 2023-06-22 | 2024-12-27 | L'oreal | Utilisation d’au moins une particule d’oxycarbonate de bismuth et d’au moins un polymère pour la filtration des rayonnements ultra-violets |
| FR3150110A1 (fr) | 2023-06-22 | 2024-12-27 | L'oreal | Matériau composite d’oxycarbonate de bismuth et d’(hydr)oxyde d’aluminium pour la filtration des rayonnements ultra-violets |
| FR3150104A1 (fr) | 2023-06-22 | 2024-12-27 | L'oreal | Matériau composite d’oxycarbonate de bismuth et de composés organiques du silicium pour la filtration des rayonnements ultra-violets |
| FR3150109A1 (fr) | 2023-06-22 | 2024-12-27 | L'oreal | Matériau composite d’oxycarbonate de bismuth et de polymères pour la filtration des rayonnements ultra-violets |
| WO2025024904A1 (en) | 2023-07-28 | 2025-02-06 | L'oreal | Cosmetic composition, use of the cosmetic composition and process for manufacturing the cosmetic composition |
| FR3157803A3 (fr) | 2023-12-27 | 2025-07-04 | L'oreal | Composition stable non collante et non huileuse avec propriété de transformation de texture |
| WO2025105505A1 (en) | 2023-11-14 | 2025-05-22 | L'oreal | Non-sticky stable composition with texture transformation property |
| FR3156034A1 (fr) | 2023-12-01 | 2025-06-06 | L'oreal | Composition comprenant un filtre UV organique lipophile, un tensioactif géminé, un polymère semi-cristallin contenant au moins une chaine d’alkyl acrylate et un polyol |
| FR3156037A1 (fr) | 2023-12-01 | 2025-06-06 | L'oreal | Composition comprenant un filtre UV organique lipophile, un tensioactif géminé et au moins 8 % en poids d’un mono-alcool en C1-C4 |
| WO2025114438A1 (en) | 2023-12-01 | 2025-06-05 | L'oreal | Composition comprising a lipophilic organic uv-screening agent, a gemini surfactant and at least 8% by weight of a c1-c4 monoalcohol |
| FR3156035A1 (fr) | 2023-12-01 | 2025-06-06 | L'oreal | Composition comprenant un filtre UV organique lipophile, un tensioactif géminé et un tensioactif anionique dérivé d’un acide aminé |
| FR3160571A3 (fr) | 2024-03-29 | 2025-10-03 | L'oreal | Compositions contenant de la bis-ethylhexyloxyphenol methoxyphenyl triazine et du dioxyde de titane |
| WO2025137039A1 (en) | 2023-12-18 | 2025-06-26 | L'oreal | Stick compositions containing bis-ethylhexyloxyphenol methoxyphenyl triazine, lipophilic gelling agent, and a solvent system |
| WO2025133698A1 (en) | 2023-12-18 | 2025-06-26 | L'oreal | Emulsions containing bis-ethylhexyloxyphenol methoxyphenyl triazine, lipophilic acrylic polymer, fatty acid ester and anionic surfactant |
| FR3160589A3 (fr) | 2024-03-29 | 2025-10-03 | L'oreal | Compositions contenant de la bis-ethylhexyloxyphenol methoxyphenyl triazine et un agent actif |
| FR3160583A3 (fr) | 2024-03-29 | 2025-10-03 | L'oreal | Compositions en baton contenant de la bis-ethylhexyloxyphenol methoxyphenyl triazine, un agent gelifiant lipophile, et un systeme de solvant |
| FR3160555A3 (fr) | 2024-03-29 | 2025-10-03 | L'oreal | Compositions colorees pour la peau contenant de la bis-ethylhexyloxyphenol methoxyphenyl triazine et un agent colorant |
| WO2025137075A1 (en) | 2023-12-18 | 2025-06-26 | L'oreal | Compositions containing bis-ethylhexyloxyphenol methoxyphenyl triazine and titanium dioxide |
| FR3160576A3 (fr) | 2024-03-29 | 2025-10-03 | L'oreal | Compositions en gel contenant de la bis-ethylhexyloxyphenol methoxyphenyl triazine et un agent gelifiant a base d’ester d’acide gras de sucre |
| FR3160572A3 (fr) | 2024-03-29 | 2025-10-03 | L'oreal | Compositions contenant un systeme absorbant les uv incluant de la bis-ethylhexyloxyphenol methoxyphenyl triazine et de l'oxyde de fer |
| WO2025137031A1 (en) | 2023-12-18 | 2025-06-26 | L'oreal | Compositions containing bis-ethylhexyloxyphenol methoxyphenyl triazine and antioxidant system |
| FR3160556A3 (fr) | 2024-03-29 | 2025-10-03 | L'oreal | Compositions de soin capillaire contenant de la bis-ethylhexyloxyphenol methoxyphenyl triazine |
| US20250195379A1 (en) | 2023-12-18 | 2025-06-19 | L'oreal | Color skin compositions containing bis-ethylhexyloxyphenol methoxyphenyl triazine and coloring agent |
| FR3160582A3 (fr) | 2024-03-29 | 2025-10-03 | L'oreal | Compositions d’emulsion contenant de la bis-ethylhexyloxyphenol methoxyphenyl triazine et un polymere semi-cristallin |
| FR3160569A3 (fr) | 2024-03-29 | 2025-10-03 | L'oreal | Compositions contenant de la bis-éthylhexyloxyphénol méthoxyphényl triazine, un polymère semi-cristallin et de la gomme de scléroglucane |
| FR3160574A3 (fr) | 2024-03-29 | 2025-10-03 | L'oreal | Compositions contenant de la bis-ethylhexyloxyphenol methoxyphenyl triazine et un agent colorant |
| FR3160575A3 (fr) | 2024-03-29 | 2025-10-03 | L'oreal | Émulsions contenant de la bis-ethylhexyloxyphenol methoxyphenyl triazine, un polymere acrylique lipophile, un ester d’acide gras et un tensioactif anionique |
| FR3160577A3 (fr) | 2024-03-29 | 2025-10-03 | L'oreal | Compositions contenant un systeme absorbant les uv contenant essentiellement de la bis-ethylhexyloxyphenol methoxyphenyl triazine et du dioxyde de titane |
| FR3160587A3 (fr) | 2024-03-29 | 2025-10-03 | L'oreal | Compositions respectueuses de l’environnement contenant de la bis-ethylhexyloxyphenol methoxyphenyl triazine |
| WO2025133699A1 (en) | 2023-12-18 | 2025-06-26 | L'oreal | Compositions containing bis-ethylhexyloxyphenol methoxyphenyl triazine, semi-crystalline polymer and scleroglucan gum |
| WO2025137033A1 (en) | 2023-12-18 | 2025-06-26 | L'oreal | Emulsion compositions containing bis-ethylhexyloxyphenol methoxyphenyl triazine and semi-crystalline polymer |
| WO2025137032A1 (en) | 2023-12-18 | 2025-06-26 | L'oreal | Compositions containing bis-ethylhexyloxyphenol methoxyphenyl triazine and active agent |
| FR3160578A3 (fr) | 2024-03-29 | 2025-10-03 | L'oreal | Compositions contenant de la bis-ethylhexyloxyphenol methoxyphenyl triazine et systeme antioxydant |
| WO2025137037A1 (en) | 2023-12-18 | 2025-06-26 | L'oreal | Gel compositions containing bis-ethylhexyloxyphenol methoxyphenyl triazine and sugar fatty acid ester gelling agent |
| FR3157116A1 (fr) | 2023-12-20 | 2025-06-27 | L'oreal | Composition cosmétique sous la forme d’une émulsion huile-dans-eau comprenant de l’acide ascorbique, au moins un filtre solaire, et gélifiée par des polymères naturels |
| WO2025132323A1 (en) | 2023-12-21 | 2025-06-26 | Dsm-Firmenich Ag | Compositions comprising a sunscreen active agent |
| WO2025141605A1 (en) | 2023-12-27 | 2025-07-03 | L'oreal | A formulation of punica granatum extract with enhanced stability and applications thereof |
| FR3157800A1 (fr) | 2023-12-28 | 2025-07-04 | L'oreal | Composition cosmétique sous la forme d’une émulsion huile-dans-eau comprenant un filtre UV organique lipophile et son utilisation en cosmétique |
| WO2025156021A1 (en) | 2024-01-24 | 2025-07-31 | L'oreal | Tinted sunscreen compositions, process for manufacturing a tinted sunscreen composition, and use of a tinted sunscreen composition |
| FR3160579A3 (fr) | 2024-03-29 | 2025-10-03 | L'oreal | Compositions contenant de la bis-ethylhexyloxyphenol methoxyphenyl triazine et un(des) filtre(s) uv organique(s) supplementaire(s) |
| FR3160558A3 (fr) | 2024-03-29 | 2025-10-03 | L'oreal | Compositions de pulverisation contenant de la bis-ethylhexyloxyphenol methoxyphenyl triazine |
| FR3160573A3 (fr) | 2024-03-29 | 2025-10-03 | L'oreal | Compositions contenant un systeme absorbant les uv incluant de la bis-ethylhexyloxyphenol methoxyphenyl triazine et de l’oxyde de zinc |
| FR3160586A3 (fr) | 2024-03-29 | 2025-10-03 | L'oreal | Compositions contenant un agent actif et des proprietes de protection contre les uv |
| FR3160584A3 (fr) | 2024-03-29 | 2025-10-03 | L'oreal | Compositions contenant de la bis-ethylhexyloxyphenol methoxyphenyl triazine et un(des) filtre(s) uv organique(s) supplementaire(s) |
| FR3160581A3 (fr) | 2024-03-29 | 2025-10-03 | L'oreal | Compositions contenant de la bis-ethylhexyloxyphenol methoxyphenyl triazine et au moins un renforçateur |
| FR3160563A3 (fr) | 2024-03-29 | 2025-10-03 | L'oreal | Compositions contenant de la bis-éthylhexyloxyphénol méthoxyphényl triazine et de l'octinoxate |
| FR3160585A3 (fr) | 2024-03-29 | 2025-10-03 | L'oreal | Compositions contenant de la bis-ethylhexyloxyphenol methoxyphenyl triazine et de l’avobenzone |
| FR3160565A3 (fr) | 2024-03-29 | 2025-10-03 | L'oreal | Compositions contenant de la bis-ethylhexyloxyphenol methoxyphenyl triazine, de l’avobenzone et un filtre uv supplementaire |
| FR3161108A1 (fr) | 2024-04-11 | 2025-10-17 | L'oreal | Composition comprenant le Drometrizole Trisiloxane, un filtre organique hydrophile, avec un ratio massique filtres organiques hydrophiles / filtres organiques lipophiles supérieur à 0,3, sans alcool |
| FR3161116A1 (fr) | 2024-04-11 | 2025-10-17 | L'oreal | Composition comprenant un filtre UV organique, un polymère gélifiant hydrophile spécifique et un ester d’acide gras et de sucre |
| FR3162628A1 (fr) | 2024-05-31 | 2025-12-05 | L'oreal | Composition comprenant un filtre UV organique lipophile solide et au moins un phospholipide |
| FR3162627A1 (fr) | 2024-06-04 | 2025-12-05 | L'oreal | Composition cosmétique comprenant des filtres UVA organiques hydrophiles ou hydrodispersibles |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| NL190101C (nl) * | 1978-11-13 | 1993-11-01 | Givaudan & Cie Sa | Dibenzoylmethaanverbinding en tegen licht beschermend preparaat. |
| EP0251398B1 (en) * | 1986-06-27 | 1992-08-12 | The Procter & Gamble Company | Novel chromophores, sunscreen compositions and methods for preventing sunburn |
| US4950467A (en) * | 1986-11-14 | 1990-08-21 | Ici Americas Inc. | Ultraviolet radiation absorbing compositions |
| US4788206A (en) * | 1987-07-10 | 1988-11-29 | Hoffmann-La Roche Inc. | Pentadieneamides |
| US5587150A (en) * | 1990-02-14 | 1996-12-24 | L'oreal | Photostable cosmetic screening composition containing a UV-A screening agent and an alkyl β, β-diphenylacrylate or α-cyano-β,β-diphenylacrylate |
| FR2658075B1 (fr) * | 1990-02-14 | 1992-05-07 | Oreal | Composition cosmetique filtrante photostable contenant un filtre uv-a et un beta,beta-diphenylacrylate ou alpha-cyano-beta,beta-diphenylacrylate d'alkyle. |
-
1998
- 1998-06-26 DE DE19828463A patent/DE19828463A1/de not_active Withdrawn
-
1999
- 1999-06-19 AT AT99111837T patent/ATE216694T1/de not_active IP Right Cessation
- 1999-06-19 EP EP99111837A patent/EP0967200B1/de not_active Expired - Lifetime
- 1999-06-19 ES ES99111837T patent/ES2177170T3/es not_active Expired - Lifetime
- 1999-06-19 DE DE59901286T patent/DE59901286D1/de not_active Expired - Fee Related
- 1999-06-21 US US09/336,733 patent/US6093385A/en not_active Expired - Fee Related
- 1999-06-25 AU AU36801/99A patent/AU757965B2/en not_active Ceased
- 1999-06-25 BR BR9902569-8A patent/BR9902569A/pt not_active Application Discontinuation
- 1999-06-26 CN CNB991097874A patent/CN1250207C/zh not_active Expired - Fee Related
- 1999-06-28 JP JP18225499A patent/JP4154084B2/ja not_active Expired - Fee Related
-
2000
- 2000-03-16 US US09/526,528 patent/US6191301B1/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| US6191301B1 (en) | 2001-02-20 |
| BR9902569A (pt) | 2000-05-02 |
| CN1242984A (zh) | 2000-02-02 |
| AU3680199A (en) | 2000-06-08 |
| DE59901286D1 (de) | 2002-05-29 |
| US6093385A (en) | 2000-07-25 |
| ES2177170T3 (es) | 2002-12-01 |
| JP2000044452A (ja) | 2000-02-15 |
| AU757965B2 (en) | 2003-03-13 |
| ATE216694T1 (de) | 2002-05-15 |
| CN1250207C (zh) | 2006-04-12 |
| DE19828463A1 (de) | 1999-12-30 |
| EP0967200A1 (de) | 1999-12-29 |
| EP0967200B1 (de) | 2002-04-24 |
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