LU85304A1 - Composition solaire filtrante contenant du polyisobutylene et son utilisation pour la protection de l'epiderme humain contre les radiations ultraviolettes - Google Patents

Composition solaire filtrante contenant du polyisobutylene et son utilisation pour la protection de l'epiderme humain contre les radiations ultraviolettes Download PDF

Info

Publication number: LU85304A1
Authority: LU; Luxembourg
Prior art keywords: composition according; camphor; rays; benzylidene; oil
Prior art date: 1984-04-13

Application number

LU85304A

Other languages

English (en)

French (fr)

Inventor

Jean-Francois Grollier

Jean Cotteret

Original Assignee

Oreal

Priority date (The priority date 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 date listed.)

1984-04-13

Filing date

1984-04-13

Publication date

1985-11-27

1984-04-13 Application filed by Oreal filed Critical Oreal

1984-04-13 Priority to LU85304A priority Critical patent/LU85304A1/fr

1985-04-10 Priority to CH1531/85A priority patent/CH662728A5/fr

1985-04-10 Priority to US06/721,673 priority patent/US4668505A/en

1985-04-12 Priority to FR8505547A priority patent/FR2562795B1/fr

1985-04-12 Priority to DE3513212A priority patent/DE3513212C2/de

1985-04-12 Priority to GB08509457A priority patent/GB2157174B/en

1985-04-12 Priority to IT67351/85A priority patent/IT1184079B/it

1985-04-12 Priority to JP60078255A priority patent/JPH062658B2/ja

1985-04-12 Priority to BE0/214835A priority patent/BE902179A/fr

1985-04-12 Priority to CA000479040A priority patent/CA1265060A/fr

1985-11-27 Publication of LU85304A1 publication Critical patent/LU85304A1/fr

1989-01-06 Priority to US07/294,985 priority patent/US4925653A/en

Links

239000000203 mixture Substances 0.000 title claims description 53
229920002367 Polyisobutene Polymers 0.000 title claims description 27
230000005855 radiation Effects 0.000 title description 8
-1 3,4,5-trihydroxy benzoyl Chemical group 0.000 claims description 30
238000001914 filtration Methods 0.000 claims description 22
DSSYKIVIOFKYAU-OIBJUYFYSA-N (S)-camphor Chemical compound C1C[C@]2(C)C(=O)C[C@H]1C2(C)C DSSYKIVIOFKYAU-OIBJUYFYSA-N 0.000 claims description 16
239000003921 oil Substances 0.000 claims description 12
239000003795 chemical substances by application Substances 0.000 claims description 10
150000001875 compounds Chemical class 0.000 claims description 9
239000000839 emulsion Substances 0.000 claims description 9
239000003755 preservative agent Substances 0.000 claims description 8
239000002304 perfume Substances 0.000 claims description 7
241000723346 Cinnamomum camphora Species 0.000 claims description 5
229930008380 camphor Natural products 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
210000003491 skin Anatomy 0.000 claims description 5
WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid group Chemical group C(C1=CC=CC=C1)(=O)O WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 claims description 4
239000002537 cosmetic Substances 0.000 claims description 4
210000002615 epidermis Anatomy 0.000 claims description 4
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 4
OIQXFRANQVWXJF-QBFSEMIESA-N (2z)-2-benzylidene-4,7,7-trimethylbicyclo[2.2.1]heptan-3-one Chemical compound CC1(C)C2CCC1(C)C(=O)\C2=C/C1=CC=CC=C1 OIQXFRANQVWXJF-QBFSEMIESA-N 0.000 claims description 3
LALVCWMSKLEQMK-UHFFFAOYSA-N 1-phenyl-3-(4-propan-2-ylphenyl)propane-1,3-dione Chemical compound C1=CC(C(C)C)=CC=C1C(=O)CC(=O)C1=CC=CC=C1 LALVCWMSKLEQMK-UHFFFAOYSA-N 0.000 claims description 3
ALYNCZNDIQEVRV-UHFFFAOYSA-N 4-aminobenzoic acid Chemical class NC1=CC=C(C(O)=O)C=C1 ALYNCZNDIQEVRV-UHFFFAOYSA-N 0.000 claims description 3
239000002250 absorbent Substances 0.000 claims description 3
239000006210 lotion Substances 0.000 claims description 3
YGSDEFSMJLZEOE-UHFFFAOYSA-M salicylate Chemical compound OC1=CC=CC=C1C([O-])=O YGSDEFSMJLZEOE-UHFFFAOYSA-M 0.000 claims description 3
229960001860 salicylate Drugs 0.000 claims description 3
229940124530 sulfonamide Drugs 0.000 claims description 3
150000003456 sulfonamides Chemical class 0.000 claims description 3
239000001993 wax Substances 0.000 claims description 3
BCMCBBGGLRIHSE-UHFFFAOYSA-N 1,3-benzoxazole Chemical class C1=CC=C2OC=NC2=C1 BCMCBBGGLRIHSE-UHFFFAOYSA-N 0.000 claims description 2
SIQJPQQLXKTTEE-UHFFFAOYSA-N 2-cinnamylidene-4,7,7-trimethylbicyclo[2.2.1]heptan-3-one Chemical compound CC1(C)C2CCC1(C)C(=O)C2=CC=CC1=CC=CC=C1 SIQJPQQLXKTTEE-UHFFFAOYSA-N 0.000 claims description 2
239000002253 acid Substances 0.000 claims description 2
239000002671 adjuvant Substances 0.000 claims description 2
239000000443 aerosol Substances 0.000 claims description 2
239000002518 antifoaming agent Substances 0.000 claims description 2
150000001555 benzenes Chemical class 0.000 claims description 2
229940114081 cinnamate Drugs 0.000 claims description 2
238000004040 coloring Methods 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
239000000975 dye Substances 0.000 claims description 2
239000003974 emollient agent Substances 0.000 claims description 2
239000003906 humectant Substances 0.000 claims description 2
239000004615 ingredient Substances 0.000 claims description 2
238000000034 method Methods 0.000 claims description 2
239000000049 pigment Substances 0.000 claims description 2
239000007787 solid Substances 0.000 claims description 2
239000004094 surface-active agent Substances 0.000 claims description 2
239000002562 thickening agent Substances 0.000 claims description 2
WBYWAXJHAXSJNI-VOTSOKGWSA-M trans-cinnamate Chemical compound [O-]C(=O)\C=C\C1=CC=CC=C1 WBYWAXJHAXSJNI-VOTSOKGWSA-M 0.000 claims description 2
239000000080 wetting agent Substances 0.000 claims description 2
WBYWAXJHAXSJNI-UHFFFAOYSA-N cinnamic acid Chemical class OC(=O)C=CC1=CC=CC=C1 WBYWAXJHAXSJNI-UHFFFAOYSA-N 0.000 claims 2
YDIYEOMDOWUDTJ-UHFFFAOYSA-N 4-(dimethylamino)benzoic acid Chemical compound CN(C)C1=CC=C(C(O)=O)C=C1 YDIYEOMDOWUDTJ-UHFFFAOYSA-N 0.000 claims 1
WDMFHQNUSVLQMS-UHFFFAOYSA-N 5-(3,3-dimethyl-2-bicyclo[2.2.1]heptanylidene)pent-3-en-2-one Chemical compound C1CC2C(C)(C)C(=CC=CC(=O)C)C1C2 WDMFHQNUSVLQMS-UHFFFAOYSA-N 0.000 claims 1
241000928106 Alain Species 0.000 claims 1
RWZYAGGXGHYGMB-UHFFFAOYSA-N anthranilic acid Chemical class NC1=CC=CC=C1C(O)=O RWZYAGGXGHYGMB-UHFFFAOYSA-N 0.000 claims 1
RWCCWEUUXYIKHB-UHFFFAOYSA-N benzophenone Chemical compound C=1C=CC=CC=1C(=O)C1=CC=CC=C1 RWCCWEUUXYIKHB-UHFFFAOYSA-N 0.000 claims 1
239000012965 benzophenone Substances 0.000 claims 1
125000003354 benzotriazolyl group Chemical class N1N=NC2=C1C=CC=C2* 0.000 claims 1
230000001143 conditioned effect Effects 0.000 claims 1
150000002148 esters Chemical class 0.000 claims 1
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 1
150000003873 salicylate salts Chemical class 0.000 claims 1
235000019198 oils Nutrition 0.000 description 11
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 10
125000000217 alkyl group Chemical group 0.000 description 8
229940099259 vaseline Drugs 0.000 description 8
PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 6
229920005987 OPPANOL® Polymers 0.000 description 6
125000004435 hydrogen atom Chemical class [H]* 0.000 description 6
239000012071 phase Substances 0.000 description 6
230000002335 preservative effect Effects 0.000 description 6
FMRHJJZUHUTGKE-UHFFFAOYSA-N Ethylhexyl salicylate Chemical compound CCCCC(CC)COC(=O)C1=CC=CC=C1O FMRHJJZUHUTGKE-UHFFFAOYSA-N 0.000 description 5
239000004698 Polyethylene Substances 0.000 description 5
239000004904 UV filter Substances 0.000 description 5
229920000573 polyethylene Polymers 0.000 description 5
150000003254 radicals Chemical class 0.000 description 5
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 4
125000003118 aryl group Chemical group 0.000 description 4
125000004432 carbon atom Chemical group C* 0.000 description 4
229960000541 cetyl alcohol Drugs 0.000 description 4
239000003086 colorant Substances 0.000 description 4
235000011187 glycerol Nutrition 0.000 description 4
229910052739 hydrogen Inorganic materials 0.000 description 4
BXWNKGSJHAJOGX-UHFFFAOYSA-N n-hexadecyl alcohol Natural products CCCCCCCCCCCCCCCCO BXWNKGSJHAJOGX-UHFFFAOYSA-N 0.000 description 4
VBICKXHEKHSIBG-UHFFFAOYSA-N 1-monostearoylglycerol Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC(O)CO VBICKXHEKHSIBG-UHFFFAOYSA-N 0.000 description 3
WYWZRNAHINYAEF-UHFFFAOYSA-N Padimate O Chemical compound CCCCC(CC)COC(=O)C1=CC=C(N(C)C)C=C1 WYWZRNAHINYAEF-UHFFFAOYSA-N 0.000 description 3
229920003171 Poly (ethylene oxide) Polymers 0.000 description 3
238000010521 absorption reaction Methods 0.000 description 3
125000003545 alkoxy group Chemical group 0.000 description 3
229960000846 camphor Drugs 0.000 description 3
239000001257 hydrogen Substances 0.000 description 3
239000007788 liquid Substances 0.000 description 3
229920000642 polymer Polymers 0.000 description 3
230000000475 sunscreen effect Effects 0.000 description 3
239000000516 sunscreening agent Substances 0.000 description 3
OULAJFUGPPVRBK-UHFFFAOYSA-N tetratriacontan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCO OULAJFUGPPVRBK-UHFFFAOYSA-N 0.000 description 3
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 2
MEZZCSHVIGVWFI-UHFFFAOYSA-N 2,2'-Dihydroxy-4-methoxybenzophenone Chemical compound OC1=CC(OC)=CC=C1C(=O)C1=CC=CC=C1O MEZZCSHVIGVWFI-UHFFFAOYSA-N 0.000 description 2
KHBQMWCZKVMBLN-UHFFFAOYSA-N Benzenesulfonamide Chemical compound NS(=O)(=O)C1=CC=CC=C1 KHBQMWCZKVMBLN-UHFFFAOYSA-N 0.000 description 2
239000004166 Lanolin Substances 0.000 description 2
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 2
230000002745 absorbent Effects 0.000 description 2
125000003342 alkenyl group Chemical group 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
229940064734 aminobenzoate Drugs 0.000 description 2
XNEFYCZVKIDDMS-UHFFFAOYSA-N avobenzone Chemical compound C1=CC(OC)=CC=C1C(=O)CC(=O)C1=CC=C(C(C)(C)C)C=C1 XNEFYCZVKIDDMS-UHFFFAOYSA-N 0.000 description 2
QRUDEWIWKLJBPS-UHFFFAOYSA-N benzotriazole Chemical compound C1=CC=C2N[N][N]C2=C1 QRUDEWIWKLJBPS-UHFFFAOYSA-N 0.000 description 2
239000012964 benzotriazole Substances 0.000 description 2
CMDKPGRTAQVGFQ-RMKNXTFCSA-N cinoxate Chemical compound CCOCCOC(=O)\C=C\C1=CC=C(OC)C=C1 CMDKPGRTAQVGFQ-RMKNXTFCSA-N 0.000 description 2
125000000753 cycloalkyl group Chemical group 0.000 description 2
CBZHHQOZZQEZNJ-UHFFFAOYSA-N ethyl 4-[bis(2-hydroxypropyl)amino]benzoate Chemical compound CCOC(=O)C1=CC=C(N(CC(C)O)CC(C)O)C=C1 CBZHHQOZZQEZNJ-UHFFFAOYSA-N 0.000 description 2
YQEMORVAKMFKLG-UHFFFAOYSA-N glycerine monostearate Natural products CCCCCCCCCCCCCCCCCC(=O)OC(CO)CO YQEMORVAKMFKLG-UHFFFAOYSA-N 0.000 description 2
SVUQHVRAGMNPLW-UHFFFAOYSA-N glycerol monostearate Natural products CCCCCCCCCCCCCCCCC(=O)OCC(O)CO SVUQHVRAGMNPLW-UHFFFAOYSA-N 0.000 description 2
125000000623 heterocyclic group Chemical group 0.000 description 2
125000002768 hydroxyalkyl group Chemical group 0.000 description 2
229940039717 lanolin Drugs 0.000 description 2
235000019388 lanolin Nutrition 0.000 description 2
125000000325 methylidene group Chemical group [H]C([H])=* 0.000 description 2
MJVGBKJNTFCUJM-UHFFFAOYSA-N mexenone Chemical compound OC1=CC(OC)=CC=C1C(=O)C1=CC=C(C)C=C1 MJVGBKJNTFCUJM-UHFFFAOYSA-N 0.000 description 2
DNIAPMSPPWPWGF-UHFFFAOYSA-N monopropylene glycol Natural products CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 2
229910052757 nitrogen Inorganic materials 0.000 description 2
125000004433 nitrogen atom Chemical group N* 0.000 description 2
229920000098 polyolefin Polymers 0.000 description 2
229950011392 sorbitan stearate Drugs 0.000 description 2
125000004178 (C1-C4) alkyl group Chemical group 0.000 description 1
DSSYKIVIOFKYAU-XCBNKYQSSA-N (R)-camphor Chemical compound C1C[C@@]2(C)C(=O)C[C@@H]1C2(C)C DSSYKIVIOFKYAU-XCBNKYQSSA-N 0.000 description 1
WHQOKFZWSDOTQP-UHFFFAOYSA-N 2,3-dihydroxypropyl 4-aminobenzoate Chemical compound NC1=CC=C(C(=O)OCC(O)CO)C=C1 WHQOKFZWSDOTQP-UHFFFAOYSA-N 0.000 description 1
ZXDDPOHVAMWLBH-UHFFFAOYSA-N 2,4-Dihydroxybenzophenone Chemical compound OC1=CC(O)=CC=C1C(=O)C1=CC=CC=C1 ZXDDPOHVAMWLBH-UHFFFAOYSA-N 0.000 description 1
IYAZLDLPUNDVAG-UHFFFAOYSA-N 2-(benzotriazol-2-yl)-4-(2,4,4-trimethylpentan-2-yl)phenol Chemical compound CC(C)(C)CC(C)(C)C1=CC=C(O)C(N2N=C3C=CC=CC3=N2)=C1 IYAZLDLPUNDVAG-UHFFFAOYSA-N 0.000 description 1
TWAOKHHZKFMFMD-UHFFFAOYSA-N 2-ethylhexyl 2-(4-phenylbenzoyl)benzoate Chemical compound CCCCC(CC)COC(=O)C1=CC=CC=C1C(=O)C1=CC=C(C=2C=CC=CC=2)C=C1 TWAOKHHZKFMFMD-UHFFFAOYSA-N 0.000 description 1
PUYOAVGNCWPANW-UHFFFAOYSA-N 2-methylpropyl 4-aminobenzoate Chemical compound CC(C)COC(=O)C1=CC=C(N)C=C1 PUYOAVGNCWPANW-UHFFFAOYSA-N 0.000 description 1
ALYNCZNDIQEVRV-UHFFFAOYSA-M 4-aminobenzoate Chemical compound NC1=CC=C(C([O-])=O)C=C1 ALYNCZNDIQEVRV-UHFFFAOYSA-M 0.000 description 1
RDBLNMQDEWOUIB-UHFFFAOYSA-N 5-methyl-2-phenyl-1,3-benzoxazole Chemical compound N=1C2=CC(C)=CC=C2OC=1C1=CC=CC=C1 RDBLNMQDEWOUIB-UHFFFAOYSA-N 0.000 description 1
POJWUDADGALRAB-PVQJCKRUSA-N Allantoin Natural products NC(=O)N[C@@H]1NC(=O)NC1=O POJWUDADGALRAB-PVQJCKRUSA-N 0.000 description 1
235000019489 Almond oil Nutrition 0.000 description 1
206010015150 Erythema Diseases 0.000 description 1
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
235000019482 Palm oil Nutrition 0.000 description 1
229920001214 Polysorbate 60 Polymers 0.000 description 1
HVUMOYIDDBPOLL-XWVZOOPGSA-N Sorbitan monostearate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O HVUMOYIDDBPOLL-XWVZOOPGSA-N 0.000 description 1
235000021355 Stearic acid Nutrition 0.000 description 1
235000019486 Sunflower oil Nutrition 0.000 description 1
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 1
239000006096 absorbing agent Substances 0.000 description 1
POJWUDADGALRAB-UHFFFAOYSA-N allantion Natural products NC(=O)NC1NC(=O)NC1=O POJWUDADGALRAB-UHFFFAOYSA-N 0.000 description 1
229960000458 allantoin Drugs 0.000 description 1
239000008168 almond oil Substances 0.000 description 1
150000001412 amines Chemical class 0.000 description 1
125000003277 amino group Chemical group 0.000 description 1
125000004103 aminoalkyl group Chemical group 0.000 description 1
229960004050 aminobenzoic acid Drugs 0.000 description 1
239000008346 aqueous phase Substances 0.000 description 1
125000003710 aryl alkyl group Chemical group 0.000 description 1
229960005274 benzocaine Drugs 0.000 description 1
150000008366 benzophenones Chemical class 0.000 description 1
150000001565 benzotriazoles Chemical class 0.000 description 1
239000001518 benzyl (E)-3-phenylprop-2-enoate Substances 0.000 description 1
230000005540 biological transmission Effects 0.000 description 1
SODJJEXAWOSSON-UHFFFAOYSA-N bis(2-hydroxy-4-methoxyphenyl)methanone Chemical compound OC1=CC(OC)=CC=C1C(=O)C1=CC=C(OC)C=C1O SODJJEXAWOSSON-UHFFFAOYSA-N 0.000 description 1
DSSYKIVIOFKYAU-UHFFFAOYSA-N camphor Chemical class C1CC2(C)C(=O)CC1C2(C)C DSSYKIVIOFKYAU-UHFFFAOYSA-N 0.000 description 1
229910052799 carbon Inorganic materials 0.000 description 1
229960001063 cinoxate Drugs 0.000 description 1
NGHOLYJTSCBCGC-UHFFFAOYSA-N cis-cinnamic acid benzyl ester Natural products C=1C=CC=CC=1C=CC(=O)OCC1=CC=CC=C1 NGHOLYJTSCBCGC-UHFFFAOYSA-N 0.000 description 1
235000009508 confectionery Nutrition 0.000 description 1
239000006071 cream Substances 0.000 description 1
125000004093 cyano group Chemical group *C#N 0.000 description 1
230000000593 degrading effect Effects 0.000 description 1
125000004985 dialkyl amino alkyl group Chemical group 0.000 description 1
229960004960 dioxybenzone Drugs 0.000 description 1
230000000694 effects Effects 0.000 description 1
231100000321 erythema Toxicity 0.000 description 1
IAJNXBNRYMEYAZ-UHFFFAOYSA-N ethyl 2-cyano-3,3-diphenylprop-2-enoate Chemical compound C=1C=CC=CC=1C(=C(C#N)C(=O)OCC)C1=CC=CC=C1 IAJNXBNRYMEYAZ-UHFFFAOYSA-N 0.000 description 1
BLFLLBZGZJTVJG-UHFFFAOYSA-N ethyl ester of p-aminobenzoic acid Natural products CCOC(=O)C1=CC=C(N)C=C1 BLFLLBZGZJTVJG-UHFFFAOYSA-N 0.000 description 1
239000003205 fragrance Substances 0.000 description 1
230000009477 glass transition Effects 0.000 description 1
125000005843 halogen group Chemical group 0.000 description 1
125000004356 hydroxy functional group Chemical group O* 0.000 description 1
125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
239000002050 international nonproprietary name Substances 0.000 description 1
125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
229960002248 meradimate Drugs 0.000 description 1
229950000999 mexenone Drugs 0.000 description 1
239000008267 milk Substances 0.000 description 1
235000013336 milk Nutrition 0.000 description 1
210000004080 milk Anatomy 0.000 description 1
QUAMTGJKVDWJEQ-UHFFFAOYSA-N octabenzone Chemical compound OC1=CC(OCCCCCCCC)=CC=C1C(=O)C1=CC=CC=C1 QUAMTGJKVDWJEQ-UHFFFAOYSA-N 0.000 description 1
OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
YBGZDTIWKVFICR-UHFFFAOYSA-N octinoxate Chemical compound CCCCC(CC)COC(=O)C=CC1=CC=C(OC)C=C1 YBGZDTIWKVFICR-UHFFFAOYSA-N 0.000 description 1
229960001679 octinoxate Drugs 0.000 description 1
239000004006 olive oil Substances 0.000 description 1
235000008390 olive oil Nutrition 0.000 description 1
229960001173 oxybenzone Drugs 0.000 description 1
229950000516 padimate Drugs 0.000 description 1
LXTZRIBXKVRLOA-UHFFFAOYSA-N padimate a Chemical compound CCCCCOC(=O)C1=CC=C(N(C)C)C=C1 LXTZRIBXKVRLOA-UHFFFAOYSA-N 0.000 description 1
239000002540 palm oil Substances 0.000 description 1
LYXOWKPVTCPORE-UHFFFAOYSA-N phenyl-(4-phenylphenyl)methanone Chemical compound C=1C=C(C=2C=CC=CC=2)C=CC=1C(=O)C1=CC=CC=C1 LYXOWKPVTCPORE-UHFFFAOYSA-N 0.000 description 1
229920006112 polar polymer Polymers 0.000 description 1
239000000843 powder Substances 0.000 description 1
238000002360 preparation method Methods 0.000 description 1
150000003902 salicylic acid esters Chemical class 0.000 description 1
150000003839 salts Chemical class 0.000 description 1
229920002545 silicone oil Polymers 0.000 description 1
239000008117 stearic acid Substances 0.000 description 1
239000002600 sunflower oil 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
- A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
- A61K8/81—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
- A61K8/8105—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
- A61K8/8111—Homopolymers or copolymers of aliphatic olefines, e.g. polyethylene, polyisobutene; Compositions of derivatives of such polymers
- 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
- 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
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S424/00—Drug, bio-affecting and body treating compositions
- Y10S424/05—Stick

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Animal Behavior & Ethology (AREA)
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Public Health (AREA)
Veterinary Medicine (AREA)
Birds (AREA)
Epidemiology (AREA)
Dermatology (AREA)
Cosmetics (AREA)

LU85304A 1984-04-13 1984-04-13 Composition solaire filtrante contenant du polyisobutylene et son utilisation pour la protection de l'epiderme humain contre les radiations ultraviolettes LU85304A1 (fr)

Priority Applications (11)

Application Number	Priority Date	Filing Date	Title
LU85304A LU85304A1 (fr)	1984-04-13	1984-04-13	Composition solaire filtrante contenant du polyisobutylene et son utilisation pour la protection de l'epiderme humain contre les radiations ultraviolettes
CH1531/85A CH662728A5 (fr)	1984-04-13	1985-04-10	Composition solaire filtrante contenant du polyisobutylene.
US06/721,673 US4668505A (en)	1984-04-13	1985-04-10	Sunscreen method containing polyisobutylene for the protection of human epidermis against ultraviolet radiations
GB08509457A GB2157174B (en)	1984-04-13	1985-04-12	Sunscreen composition containing polyisobutylene
DE3513212A DE3513212C2 (de)	1984-04-13	1985-04-12	Sonnenschutzmittel
FR8505547A FR2562795B1 (fr)	1984-04-13	1985-04-12	Composition solaire filtrante contenant du polyisobutylene et son utilisation pour la protection de l'epiderme humain contre les radiations ultraviolettes
IT67351/85A IT1184079B (it)	1984-04-13	1985-04-12	Composizione filtrante i raggi solari contenente poliisobutilene e suo impiego per la protezione dell epidermide umana contro le radiazioni ultraviolette
JP60078255A JPH062658B2 (ja)	1984-04-13	1985-04-12	日光濾光性組成物
BE0/214835A BE902179A (fr)	1984-04-13	1985-04-12	Composition solaire filtrante contenant du polyisobutylene et son utilisation pour la protection de l'epiderme humain contre les radiations ultra-violettes.
CA000479040A CA1265060A (fr)	1984-04-13	1985-04-12	Composition solaire filtrante contenant du polyisobutylene et son utilisation pour la protection de l'epiderme humain contre les radiations ultraviolettes
US07/294,985 US4925653A (en)	1984-04-13	1989-01-06	Sunscreen composition containing polyisobutylene and its use for the protection of human epidermis against ultraviolet radiations

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
LU85304		1984-04-13
LU85304A LU85304A1 (fr)	1984-04-13	1984-04-13	Composition solaire filtrante contenant du polyisobutylene et son utilisation pour la protection de l'epiderme humain contre les radiations ultraviolettes

Publications (1)

Publication Number	Publication Date
LU85304A1 true LU85304A1 (fr)	1985-11-27

Family

ID=19730243

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
LU85304A LU85304A1 (fr)	1984-04-13	1984-04-13	Composition solaire filtrante contenant du polyisobutylene et son utilisation pour la protection de l'epiderme humain contre les radiations ultraviolettes

Country Status (10)

Country	Link
US (2)	US4668505A (ja)
JP (1)	JPH062658B2 (ja)
BE (1)	BE902179A (ja)
CA (1)	CA1265060A (ja)
CH (1)	CH662728A5 (ja)
DE (1)	DE3513212C2 (ja)
FR (1)	FR2562795B1 (ja)
GB (1)	GB2157174B (ja)
IT (1)	IT1184079B (ja)
LU (1)	LU85304A1 (ja)

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* Cited by examiner, † Cited by third party
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LU86703A1 (fr) *	1986-12-08	1988-07-14	Oreal	Composition cosmetique photostable contenant un filtre uv-a et un filtre uv-b,son utilisation pour la protection de la peau contre les rayons uv et procede de stabilisation du filtre uv-a par le filtre uv-b
LU86997A1 (fr) *	1987-09-21	1989-04-06	Oreal	Composition cosmetique filtrante photostable contenant de la bixine associee a un filtre uv liposoluble et son utilisation pour la protection de l'epiderme humain contre les radiations ultraviolettes
US5223250A (en) *	1991-02-05	1993-06-29	Sun Smart, Inc.	Visibly transparent UV sunblock cosmetic compositions
AU668862B2 (en) *	1991-02-05	1996-05-23	Basf Corporation	Visibly transparent UV sunblock agents and methods of making same
GB9208653D0 (en) *	1992-04-22	1992-06-10	Unilever Plc	Cosmetic composition and process for making it
CA2142298A1 (en) *	1992-08-13	1994-03-03	George E. Deckner	Photostable sunscreen compositions
FR2720635B1 (fr) *	1994-06-03	1996-07-26	Oreal	Compositions cosmétiques antisolaires et utilisations.
FR2727115B1 (fr) *	1994-11-17	1996-12-27	Oreal	Nouveaux filtres solaires, compositions cosmetiques photoprotectrices les contenant et utilisations
US6004540A (en) *	1994-11-17	1999-12-21	Societe L'oreal S.A.	Photoprotective/cosmetic compositions comprising sulfonamido-functional polyorganosiloxanes/polyorganosilanes
AU3692097A (en) *	1996-08-02	1998-02-25	Plum Kemi Produktion A/S	An oil-in-water emulsion for use on human skin for cleansing, preserving or improving the condition of the skin
WO1999027039A1 (en) *	1997-11-25	1999-06-03	General Technology Applications, Inc.	High molecular weight polymer additive for coating and lubricating products
US6312672B1 (en)	1999-10-29	2001-11-06	Exxon Mobil Chemical Patents Inc.	Sunscreen compositions containing copolymers of isoprene butadiene and/or styrene to provide improved water resistance
EP1111034A1 (en) *	1999-12-22	2001-06-27	The Procter & Gamble Company	Laundry and cleaning and/or fabric care compositions
FR2811546B1 (fr) *	2000-07-13	2003-09-26	Oreal	Kit et procede de maquillage longue tenue
FR2811548B1 (fr) *	2000-07-13	2002-08-23	Oreal	Composition cosmetique pulverulente longue tenue comprenant un materiau adhesif particulier
US6444195B1 (en)	2001-06-18	2002-09-03	Johnson & Johnson Consumer Companies, Inc.	Sunscreen compositions containing a dibenzoylmethane derivative
FR2827510B1 (fr) *	2001-07-18	2005-07-01	Oreal	Filtres uv organiques insolubles de type aryl vinylene cetone et leur utilisation en cosmetique
DE10162844A1 (de) *	2001-12-20	2003-07-03	Beiersdorf Ag	Kosmetische und dermatologische Lichtschutzformulierungen mit einem Gehalt an Bis-Resorcinyltriazinderivaten und Benzoxazol-Derivaten
DE10162842A1 (de) *	2001-12-20	2003-07-03	Beiersdorf Ag	Kosmetische und dermatologische Lichtschutzformulierungen mit einem Gehalt an Benzotriazolen und Benzoxazol-Derivaten
DE10162840A1 (de) *	2001-12-20	2003-07-03	Beiersdorf Ag	Kosmetische und dermatologische Lichtschutzformulierungen mit einem Gehalt an wasserlöslichen UV-Filtersubstanzen und Benzoxazol-Derivaten
WO2003053393A1 (de)	2001-12-20	2003-07-03	Beiersdorf Ag	Komestiche und dermatologische lichtschutzformulierungen mit einem gehalt an hydroxybenzophenonen und benzoxazol-derivaten
DE102005015632A1 (de) *	2005-04-05	2006-10-12	Basf Ag	Verwendung von Polyisobuten enthaltenden Copolymerisaten in Lichtschutzmitteln
AU2011250962B2 (en)	2010-05-10	2015-09-03	Gfbiochemicals Limited	Personal care formulations containing alkyl ketal esters and methods of manufacture
JP5841374B2 (ja) *	2011-08-05	2016-01-13	株式会社資生堂	水中油型乳化下地化粧料
KR101378554B1 (ko) *	2012-01-29	2014-03-27	(주)바이오제닉스	자외선 차단 조성물 및 이의 제조 방법
JP2016506383A (ja)	2012-11-29	2016-03-03	サジティス・インコーポレイテッド	カルボキシエステルケタール、その製造方法および使用
CN109843259B (zh) *	2016-10-31	2022-04-26	株式会社资生堂	水包油型皮肤外用组合物
CN115300493A (zh) *	2022-07-12	2022-11-08	厦门大学	核受体RXRα配体的应用及抗肿瘤药物

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US2085693A (en) *	1933-04-20	1937-06-29	Standard Oil Dev Co	Preparation of mineral white oils and products prepared therefrom
US2312715A (en) *	1939-10-04	1943-03-02	Stanco Inc	Emulsion for burn treatment
US2628187A (en) *	1950-05-06	1953-02-10	Res Prod Corp	Medicinal mineral oil vehicle thickened with polyethylene
FR1184532A (fr) *	1955-11-19	1959-07-22		Perfectionnements aux préparations pour la peau et aux procédés d'obtention
US3239483A (en) *	1960-08-08	1966-03-08	Exxon Research Engineering Co	Stabilization of polyisobutylene polymers with sulfur and benzotriazoles
FR1295370A (fr) *	1960-08-09	1962-06-08		Support émulsionnant et adhérent pour préparations thérapeutiques
DE1792472A1 (de) *	1968-09-05	1971-04-08	Henkel & Cie Gmbh	Kunstvaseline
GB1300223A (en) *	1969-03-07	1972-12-20	Askvold B	Makeup preparations
US4164563A (en) *	1975-03-24	1979-08-14	Minnesota Mining And Manufacturing Company	Non-greasy compositions
AU528642B2 (en) *	1978-07-19	1983-05-05	Charles Of The Ritz Group Ltd.	Sunblock formulation
US4264581A (en) *	1979-07-02	1981-04-28	Eli Lilly And Company	Sunscreen composition
JPS57123112A (en) *	1980-12-30	1982-07-31	Union Carbide Corp	Effect increase of local composition

1984
- 1984-04-13 LU LU85304A patent/LU85304A1/fr unknown
1985
- 1985-04-10 CH CH1531/85A patent/CH662728A5/fr not_active IP Right Cessation
- 1985-04-10 US US06/721,673 patent/US4668505A/en not_active Expired - Fee Related
- 1985-04-12 CA CA000479040A patent/CA1265060A/fr not_active Expired - Lifetime
- 1985-04-12 JP JP60078255A patent/JPH062658B2/ja not_active Expired - Lifetime
- 1985-04-12 GB GB08509457A patent/GB2157174B/en not_active Expired
- 1985-04-12 IT IT67351/85A patent/IT1184079B/it active
- 1985-04-12 BE BE0/214835A patent/BE902179A/fr not_active IP Right Cessation
- 1985-04-12 FR FR8505547A patent/FR2562795B1/fr not_active Expired
- 1985-04-12 DE DE3513212A patent/DE3513212C2/de not_active Expired - Fee Related
1989
- 1989-01-06 US US07/294,985 patent/US4925653A/en not_active Expired - Fee Related

Also Published As

Publication number	Publication date
JPS60237013A (ja)	1985-11-25
US4668505A (en)	1987-05-26
DE3513212A1 (de)	1985-10-24
IT8567351A1 (it)	1986-10-12
CH662728A5 (fr)	1987-10-30
GB2157174A (en)	1985-10-23
US4925653A (en)	1990-05-15
CA1265060A (fr)	1990-01-30
IT1184079B (it)	1987-10-22
DE3513212C2 (de)	1997-05-07
BE902179A (fr)	1985-10-14
FR2562795B1 (fr)	1988-03-11
GB8509457D0 (en)	1985-05-15
JPH062658B2 (ja)	1994-01-12
GB2157174B (en)	1987-11-18
FR2562795A1 (fr)	1985-10-18
IT8567351A0 (it)	1985-04-12

Publication	Publication Date	Title
LU85304A1 (fr)	1985-11-27	Composition solaire filtrante contenant du polyisobutylene et son utilisation pour la protection de l'epiderme humain contre les radiations ultraviolettes
CA2065117C (fr)	2002-12-24	Derives s-triaziniques portant des substituants benzalmalonates, leur procede de preparation, compositions cosmetiques filtrantes les contenant et leur utilisation pour proteger la peau et les cheveux du rayonnement ultraviolet
EP0815834B1 (fr)	2000-12-20	Compositions cosmétiques filtrantes photostabilisées comprenant un dérivé de dibenzoylméthane et un composé amidé
CA1202327A (fr)	1986-03-25	Compositions cosmetiques contenant des derives hydroxy les du dibenzoylmethane et leur utilisation pour la pr otection de l'epiderme humain contre les rayons ultrav iolets, nouveaux derives hydroxyles du dibenzoylmethan e utilises et leur procede de preparation
CA2222377C (fr)	2004-07-13	Compositions comprenant un derive de dibenzoylmethane, un derive de 1,3,5-triazine et un compose amide et utilisations
CA1258638A (fr)	1989-08-22	Composition cosmetique contenant de l'aloesine a titre d'agent de protection contre la lumiere solaire et son utilisation pour la protection de la peau et des cheveux
CA2064930A1 (fr)	1992-10-05	Derives de s-triaziniques portant des substituants benzylidene camphre, leur procede de preparation, compositions cosmetiques filtrantes les contenant et leur utilisation pour proteger la peau et les cheveux contre les rayonnements ultraviolets
CA1307468C (fr)	1992-09-15	Composition cosmetique filtrante photostable contenant de la bixine associee a un filtre uv liposoluble et son utilisation pour la protection de l'epiderme humain contre les radiations ultraviolettes
FR2719481A1 (fr)	1995-11-10	Composition à base de composés antifongiques et de composés antibactériens halogènes pour diminuer la chute des cheveux.
EP0848945B1 (fr)	1999-10-06	Compositions comprenant un dérivé de dibenzoylméthane, un dérivé de 1,3,5-triazine et un dérivé silicié à fonction benzalmalonate et utilisations
LU86601A1 (fr)	1988-04-05	Composition cosmetique photostable contenant un derive d'ethylrutine a titre d'agent de protection contre la lumiere salaire et son utilisation pour la protection de la peau et des cheveux
CA2001742A1 (fr)	1990-04-28	Compositions cosmetiques filtrantes, leur utilisation pour la protection de la peau et des cheveux contre le rayonnement ultraviolet,nouveau derives de la 5-benzylidene 3-oxa cyclopentanone utilises dans ces compositions et leur procede de preparation
FR2757055A1 (fr)	1998-06-19	Compositions comprenant un derive de dibenzoylmethane, un derive de 1,2,3-triazine et un benzalmalonate de dialkyle et utilisations
EP0982310B1 (fr)	2004-03-31	Procédé de photostabilisation de filtres solaires dérivés du dibenzoylméthane, compositions cosmétiques filtrantes photostabilisées ainsi obtenues et leurs utilisations.
EP0970961B1 (fr)	2001-04-25	Procédé de photostabilisation de filtres solaires dérivés du dibenzoylméthane, compositions cosmétiques filtrantes photostabilisées ainsi obtenues et leurs utilisations
EP0685228B1 (fr)	1999-06-30	Compositions cosmétiques antisolaires à base d'un mélange synergétique de filtres et utilisations
EP0389337A1 (fr)	1990-09-26	Utilisation en cosmétique de diorganopolysiloxanes à fonction hydroxy-2 benzophénone et compositions contenant ces composés, destinées à la protection de la peau et des cheveux
CH649987A5 (fr)	1985-06-28	Derives de dibenzoylmethane quaternaire, leur utilisation comme agent filtrant solaire et composition cosmetique les contenant.
CH675580A5 (ja)	1990-10-15
EP0383655A1 (fr)	1990-08-22	Utilisation en cosmétique de diorganopolysiloxanes à fonction dibenzoyleméthane et nouvelles compositions cosmétiques contenant ces composés, destinées à la protection de la peau et des cheveux
CA1292700C (fr)	1991-12-03	Compositions cosmetiques destinees a proteger la peau contre les effets indesires des radiations ultraviolettes
FR2645145A1 (fr)	1990-10-05	Compositions cosmetiques et pharmaceutiques contenant des derives lipophiles du benzylidene camphre et nouveaux derives lipophiles du benzylidene camphre
FR2526658A2 (fr)	1983-11-18	Compositions cosmetiques contenant des derives hydroxyles du dibenzoylmethane et leur utilisation pour la protection de l'epiderme humain contre les rayons ultraviolets, nouveaux derives hydroxyles du dibenzoylmethane utilises et leur procede de preparation
CH679668A5 (ja)	1992-03-31
CA2201959C (fr)	2001-07-24	Composition filtrante photostable comprenant un derive de dibenzoylmethane et un alkylether de polysaccharide et ses utilisations