CA2029240C - Compositions de photoprotection ayant une meilleure substantivite - Google Patents

Compositions de photoprotection ayant une meilleure substantivite

Info

Publication number: CA2029240C
Authority: CA; Canada
Prior art keywords: ethylhexyl; group; mixtures; sunscreen; composition according
Prior art date: 1990-11-02
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.): Expired - Lifetime

Application number

CA 2029240

Other languages

English (en)

Other versions

CA2029240A1 (fr

Inventor

Frederick Winfield Woodin, Jr.

George Endel Deckner

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

Richardson Vicks Inc

Original Assignee

Richardson Vicks Inc

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.)

1990-11-02

Filing date

1990-11-02

Publication date

1998-12-01

1990-11-02 Application filed by Richardson Vicks Inc filed Critical Richardson Vicks Inc

1990-11-02 Priority to CA 2029240 priority Critical patent/CA2029240C/fr

1992-05-03 Publication of CA2029240A1 publication Critical patent/CA2029240A1/fr

1998-12-01 Application granted granted Critical

1998-12-01 Publication of CA2029240C publication Critical patent/CA2029240C/fr

2010-11-02 Anticipated expiration legal-status Critical

Status Expired - Lifetime legal-status Critical Current

Links

239000000203 mixture Substances 0.000 title claims abstract description 76
230000003711 photoprotective effect Effects 0.000 title description 7
230000000699 topical effect Effects 0.000 claims abstract description 16
239000000516 sunscreening agent Substances 0.000 claims description 49
-1 TEA stearate salts Chemical class 0.000 claims description 41
239000001993 wax Substances 0.000 claims description 37
230000000475 sunscreen effect Effects 0.000 claims description 35
235000014113 dietary fatty acids Nutrition 0.000 claims description 20
239000000194 fatty acid Substances 0.000 claims description 20
229930195729 fatty acid Natural products 0.000 claims description 20
150000004665 fatty acids Chemical class 0.000 claims description 20
DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 claims description 16
239000003974 emollient agent Substances 0.000 claims description 16
239000002253 acid Substances 0.000 claims description 14
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims description 13
150000005690 diesters Chemical class 0.000 claims description 12
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 12
239000000839 emulsion Substances 0.000 claims description 11
239000000178 monomer Substances 0.000 claims description 11
239000003995 emulsifying agent Substances 0.000 claims description 10
150000002148 esters Chemical class 0.000 claims 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 claims description 9
230000000694 effects Effects 0.000 claims description 9
PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 claims description 8
NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 8
DXGLGDHPHMLXJC-UHFFFAOYSA-N oxybenzone Chemical compound OC1=CC(OC)=CC=C1C(=O)C1=CC=CC=C1 DXGLGDHPHMLXJC-UHFFFAOYSA-N 0.000 claims description 8
DCXXMTOCNZCJGO-UHFFFAOYSA-N tristearoylglycerol Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC(OC(=O)CCCCCCCCCCCCCCCCC)COC(=O)CCCCCCCCCCCCCCCCC DCXXMTOCNZCJGO-UHFFFAOYSA-N 0.000 claims description 8
125000004432 carbon atom Chemical group C* 0.000 claims description 7
239000008172 hydrogenated vegetable oil Substances 0.000 claims description 7
UFTFJSFQGQCHQW-UHFFFAOYSA-N triformin Chemical compound O=COCC(OC=O)COC=O UFTFJSFQGQCHQW-UHFFFAOYSA-N 0.000 claims description 7
229920002126 Acrylic acid copolymer Polymers 0.000 claims description 6
229910019142 PO4 Inorganic materials 0.000 claims description 6
125000000217 alkyl group Chemical group 0.000 claims description 6
238000004132 cross linking Methods 0.000 claims description 6
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 6
235000021317 phosphate Nutrition 0.000 claims description 6
150000005846 sugar alcohols Polymers 0.000 claims description 6
150000007513 acids Chemical class 0.000 claims description 5
239000003513 alkali Substances 0.000 claims description 5
229940078812 myristyl myristate Drugs 0.000 claims description 5
DZKXJUASMGQEMA-UHFFFAOYSA-N tetradecyl tetradecanoate Chemical compound CCCCCCCCCCCCCCOC(=O)CCCCCCCCCCCCC DZKXJUASMGQEMA-UHFFFAOYSA-N 0.000 claims description 5
DMBUODUULYCPAK-UHFFFAOYSA-N 1,3-bis(docosanoyloxy)propan-2-yl docosanoate Chemical compound CCCCCCCCCCCCCCCCCCCCCC(=O)OCC(OC(=O)CCCCCCCCCCCCCCCCCCCCC)COC(=O)CCCCCCCCCCCCCCCCCCCCC DMBUODUULYCPAK-UHFFFAOYSA-N 0.000 claims description 4
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 claims description 4
BANXPJUEBPWEOT-UHFFFAOYSA-N 2-methyl-Pentadecane Chemical compound CCCCCCCCCCCCCC(C)C BANXPJUEBPWEOT-UHFFFAOYSA-N 0.000 claims description 4
239000004721 Polyphenylene oxide Substances 0.000 claims description 4
SCMSRHIBVBIECI-UHFFFAOYSA-N [2-hydroxy-4-(2-hydroxyethoxy)phenyl]-phenylmethanone Chemical compound OC1=CC(OCCO)=CC=C1C(=O)C1=CC=CC=C1 SCMSRHIBVBIECI-UHFFFAOYSA-N 0.000 claims description 4
150000001298 alcohols Chemical class 0.000 claims description 4
125000003342 alkenyl group Chemical group 0.000 claims description 4
229960004050 aminobenzoic acid Drugs 0.000 claims description 4
229960005193 avobenzone Drugs 0.000 claims description 4
229940110456 cocoa butter Drugs 0.000 claims description 4
235000019868 cocoa butter Nutrition 0.000 claims description 4
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 4
235000011187 glycerol Nutrition 0.000 claims description 4
239000001257 hydrogen Substances 0.000 claims description 4
229910052739 hydrogen Inorganic materials 0.000 claims description 4
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 4
YAGMLECKUBJRNO-UHFFFAOYSA-N octyl 4-(dimethylamino)benzoate Chemical compound CCCCCCCCOC(=O)C1=CC=C(N(C)C)C=C1 YAGMLECKUBJRNO-UHFFFAOYSA-N 0.000 claims description 4
150000003013 phosphoric acid derivatives Chemical class 0.000 claims description 4
229920000570 polyether Polymers 0.000 claims description 4
229940098780 tribehenin Drugs 0.000 claims description 4
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 claims description 3
WCOXQTXVACYMLM-UHFFFAOYSA-N 2,3-bis(12-hydroxyoctadecanoyloxy)propyl 12-hydroxyoctadecanoate Chemical compound CCCCCCC(O)CCCCCCCCCCC(=O)OCC(OC(=O)CCCCCCCCCCC(O)CCCCCC)COC(=O)CCCCCCCCCCC(O)CCCCCC WCOXQTXVACYMLM-UHFFFAOYSA-N 0.000 claims description 3
ZXDDPOHVAMWLBH-UHFFFAOYSA-N 2,4-Dihydroxybenzophenone Chemical compound OC1=CC(O)=CC=C1C(=O)C1=CC=CC=C1 ZXDDPOHVAMWLBH-UHFFFAOYSA-N 0.000 claims description 3
KGKQNDQDVZQTAG-UHFFFAOYSA-N 8-methylnonyl 2,2-dimethylpropanoate Chemical compound CC(C)CCCCCCCOC(=O)C(C)(C)C KGKQNDQDVZQTAG-UHFFFAOYSA-N 0.000 claims description 3
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 3
239000002202 Polyethylene glycol Substances 0.000 claims description 3
229930006000 Sucrose Natural products 0.000 claims description 3
CZMRCDWAGMRECN-UGDNZRGBSA-N Sucrose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 CZMRCDWAGMRECN-UGDNZRGBSA-N 0.000 claims description 3
125000002511 behenyl 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])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([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 claims description 3
125000001033 ether group Chemical group 0.000 claims description 3
RUIQFBSZLHXKCA-UHFFFAOYSA-N hexadecyl hydroxy hydrogen phosphate Chemical compound CCCCCCCCCCCCCCCCOP(O)(=O)OO RUIQFBSZLHXKCA-UHFFFAOYSA-N 0.000 claims description 3
125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 3
WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 claims description 3
125000005395 methacrylic acid group Chemical group 0.000 claims description 3
239000004200 microcrystalline wax Substances 0.000 claims description 3
235000019808 microcrystalline wax Nutrition 0.000 claims description 3
229940078555 myristyl propionate Drugs 0.000 claims description 3
239000012188 paraffin wax Substances 0.000 claims description 3
229920000728 polyester Polymers 0.000 claims description 3
229920001223 polyethylene glycol Polymers 0.000 claims description 3
229920001451 polypropylene glycol Polymers 0.000 claims description 3
238000006467 substitution reaction Methods 0.000 claims description 3
239000005720 sucrose Substances 0.000 claims description 3
YRZGMTHQPGNLEK-UHFFFAOYSA-N tetradecyl propionate Chemical compound CCCCCCCCCCCCCCOC(=O)CC YRZGMTHQPGNLEK-UHFFFAOYSA-N 0.000 claims description 3
150000003626 triacylglycerols Chemical class 0.000 claims description 3
229940043268 2,2,4,4,6,8,8-heptamethylnonane Drugs 0.000 claims description 2
UONRGKALIXPQDW-UHFFFAOYSA-N C1=CC(N(C)CC(CC)CCCC)=CC=C1C(=O)OCCOC1=CC=C(C(=O)CC(=O)C=2C=CC=CC=2)C=C1 Chemical compound C1=CC(N(C)CC(CC)CCCC)=CC=C1C(=O)OCCOC1=CC=C(C(=O)CC(=O)C=2C=CC=CC=2)C=C1 UONRGKALIXPQDW-UHFFFAOYSA-N 0.000 claims description 2
FMRHJJZUHUTGKE-UHFFFAOYSA-N Ethylhexyl salicylate Chemical compound CCCCC(CC)COC(=O)C1=CC=CC=C1O FMRHJJZUHUTGKE-UHFFFAOYSA-N 0.000 claims description 2
239000004166 Lanolin Substances 0.000 claims description 2
239000004264 Petrolatum Substances 0.000 claims description 2
235000018936 Vitellaria paradoxa Nutrition 0.000 claims description 2
241001135917 Vitellaria paradoxa Species 0.000 claims description 2
229940098781 c18-36 acid triglyceride Drugs 0.000 claims description 2
229940061587 calcium behenate Drugs 0.000 claims description 2
SMBKCSPGKDEPFO-UHFFFAOYSA-L calcium;docosanoate Chemical compound [Ca+2].CCCCCCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCCCCCC([O-])=O SMBKCSPGKDEPFO-UHFFFAOYSA-L 0.000 claims description 2
NZZIMKJIVMHWJC-UHFFFAOYSA-N dibenzoylmethane Chemical compound C=1C=CC=CC=1C(=O)CC(=O)C1=CC=CC=C1 NZZIMKJIVMHWJC-UHFFFAOYSA-N 0.000 claims description 2
229940068171 ethyl hexyl salicylate Drugs 0.000 claims description 2
KUVMKLCGXIYSNH-UHFFFAOYSA-N isopentadecane Natural products CCCCCCCCCCCCC(C)C KUVMKLCGXIYSNH-UHFFFAOYSA-N 0.000 claims description 2
229940039717 lanolin Drugs 0.000 claims description 2
235000019388 lanolin Nutrition 0.000 claims description 2
WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 claims description 2
229940066842 petrolatum Drugs 0.000 claims description 2
235000019271 petrolatum Nutrition 0.000 claims description 2
229940057910 shea butter Drugs 0.000 claims description 2
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 claims 1
239000011248 coating agent Substances 0.000 claims 1
238000000576 coating method Methods 0.000 claims 1
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 claims 1
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 claims 1
229940097789 heavy mineral oil Drugs 0.000 claims 1
229940059904 light mineral oil Drugs 0.000 claims 1
206010042496 Sunburn Diseases 0.000 abstract description 4
206010063493 Premature ageing Diseases 0.000 abstract description 3
208000032038 Premature aging Diseases 0.000 abstract description 3
238000004078 waterproofing Methods 0.000 abstract description 3
230000009931 harmful effect Effects 0.000 abstract description 2
LXCFILQKKLGQFO-UHFFFAOYSA-N methylparaben Chemical compound COC(=O)C1=CC=C(O)C=C1 LXCFILQKKLGQFO-UHFFFAOYSA-N 0.000 description 14
QELSKZZBTMNZEB-UHFFFAOYSA-N propylparaben Chemical compound CCCOC(=O)C1=CC=C(O)C=C1 QELSKZZBTMNZEB-UHFFFAOYSA-N 0.000 description 14
230000005855 radiation Effects 0.000 description 12
238000000034 method Methods 0.000 description 10
229920002125 Sokalan® Polymers 0.000 description 9
230000006378 damage Effects 0.000 description 9
230000001154 acute effect Effects 0.000 description 8
239000003795 chemical substances by application Substances 0.000 description 8
230000001684 chronic effect Effects 0.000 description 8
239000002537 cosmetic Substances 0.000 description 8
239000007764 o/w emulsion Substances 0.000 description 8
229920002545 silicone oil Polymers 0.000 description 8
206010015150 Erythema Diseases 0.000 description 7
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 7
GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 7
229920001577 copolymer Polymers 0.000 description 7
231100000321 erythema Toxicity 0.000 description 7
239000003205 fragrance Substances 0.000 description 7
239000000463 material Substances 0.000 description 7
239000004292 methyl p-hydroxybenzoate Substances 0.000 description 7
235000010270 methyl p-hydroxybenzoate Nutrition 0.000 description 7
229960002216 methylparaben Drugs 0.000 description 7
229920000642 polymer Polymers 0.000 description 7
239000004405 propyl p-hydroxybenzoate Substances 0.000 description 7
235000010232 propyl p-hydroxybenzoate Nutrition 0.000 description 7
229960003415 propylparaben Drugs 0.000 description 7
WVDDGKGOMKODPV-UHFFFAOYSA-N Benzyl alcohol Chemical compound OCC1=CC=CC=C1 WVDDGKGOMKODPV-UHFFFAOYSA-N 0.000 description 6
XMSXQFUHVRWGNA-UHFFFAOYSA-N Decamethylcyclopentasiloxane Chemical compound C[Si]1(C)O[Si](C)(C)O[Si](C)(C)O[Si](C)(C)O[Si](C)(C)O1 XMSXQFUHVRWGNA-UHFFFAOYSA-N 0.000 description 6
229920000435 poly(dimethylsiloxane) Polymers 0.000 description 6
238000009472 formulation Methods 0.000 description 5
229960001679 octinoxate Drugs 0.000 description 5
229920001296 polysiloxane Polymers 0.000 description 5
KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 4
229940086555 cyclomethicone Drugs 0.000 description 4
235000013870 dimethyl polysiloxane Nutrition 0.000 description 4
239000012530 fluid Substances 0.000 description 4
229930195733 hydrocarbon Natural products 0.000 description 4
150000002430 hydrocarbons Chemical class 0.000 description 4
230000007774 longterm Effects 0.000 description 4
125000000325 methylidene group Chemical group [H]C([H])=* 0.000 description 4
229960001173 oxybenzone Drugs 0.000 description 4
230000037072 sun protection Effects 0.000 description 4
BDEHGQOUMOLWCN-UHFFFAOYSA-N 16-methylheptadecyl benzoate Chemical compound CC(C)CCCCCCCCCCCCCCCOC(=O)C1=CC=CC=C1 BDEHGQOUMOLWCN-UHFFFAOYSA-N 0.000 description 3
ALYNCZNDIQEVRV-UHFFFAOYSA-N 4-aminobenzoic acid Chemical compound NC1=CC=C(C(O)=O)C=C1 ALYNCZNDIQEVRV-UHFFFAOYSA-N 0.000 description 3
FPVVYTCTZKCSOJ-UHFFFAOYSA-N Ethylene glycol distearate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCCOC(=O)CCCCCCCCCCCCCCCCC FPVVYTCTZKCSOJ-UHFFFAOYSA-N 0.000 description 3
125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 3
150000001875 compounds Chemical class 0.000 description 3
125000004122 cyclic group Chemical group 0.000 description 3
WSDISUOETYTPRL-UHFFFAOYSA-N dmdm hydantoin Chemical compound CC1(C)N(CO)C(=O)N(CO)C1=O WSDISUOETYTPRL-UHFFFAOYSA-N 0.000 description 3
238000005516 engineering process Methods 0.000 description 3
239000000126 substance Substances 0.000 description 3
MYRTYDVEIRVNKP-UHFFFAOYSA-N 1,2-Divinylbenzene Chemical compound C=CC1=CC=CC=C1C=C MYRTYDVEIRVNKP-UHFFFAOYSA-N 0.000 description 2
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 description 2
SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 2
RFVNOJDQRGSOEL-UHFFFAOYSA-N 2-hydroxyethyl octadecanoate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCCO RFVNOJDQRGSOEL-UHFFFAOYSA-N 0.000 description 2
WLAMNBDJUVNPJU-UHFFFAOYSA-N 2-methylbutyric acid Chemical compound CCC(C)C(O)=O WLAMNBDJUVNPJU-UHFFFAOYSA-N 0.000 description 2
XMFXBMLFOSSELI-UHFFFAOYSA-N 2-octyldodecyl 12-octadecanoyloxyoctadecanoate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OC(CCCCCC)CCCCCCCCCCC(=O)OCC(CCCCCCCC)CCCCCCCCCC XMFXBMLFOSSELI-UHFFFAOYSA-N 0.000 description 2
FSEXLNMNADBYJU-UHFFFAOYSA-N 2-phenylquinoline Chemical compound C1=CC=CC=C1C1=CC=C(C=CC=C2)C2=N1 FSEXLNMNADBYJU-UHFFFAOYSA-N 0.000 description 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 description 2
QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 2
RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 description 2
ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 2
GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 2
UPOYFZYFGWBUKL-UHFFFAOYSA-N amiphenazole Chemical compound S1C(N)=NC(N)=C1C1=CC=CC=C1 UPOYFZYFGWBUKL-UHFFFAOYSA-N 0.000 description 2
229950001798 amiphenazole Drugs 0.000 description 2
RWZYAGGXGHYGMB-UHFFFAOYSA-N anthranilic acid Chemical class NC1=CC=CC=C1C(O)=O RWZYAGGXGHYGMB-UHFFFAOYSA-N 0.000 description 2
239000002585 base Substances 0.000 description 2
235000019445 benzyl alcohol Nutrition 0.000 description 2
230000002939 deleterious effect Effects 0.000 description 2
DLAHAXOYRFRPFQ-UHFFFAOYSA-N dodecyl benzoate Chemical compound CCCCCCCCCCCCOC(=O)C1=CC=CC=C1 DLAHAXOYRFRPFQ-UHFFFAOYSA-N 0.000 description 2
RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
UQEAIHBTYFGYIE-UHFFFAOYSA-N hexamethyldisiloxane Chemical compound C[Si](C)(C)O[Si](C)(C)C UQEAIHBTYFGYIE-UHFFFAOYSA-N 0.000 description 2
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 2
239000004615 ingredient Substances 0.000 description 2
230000000670 limiting effect Effects 0.000 description 2
238000004519 manufacturing process Methods 0.000 description 2
VAMXMNNIEUEQDV-UHFFFAOYSA-N methyl anthranilate Chemical compound COC(=O)C1=CC=CC=C1N VAMXMNNIEUEQDV-UHFFFAOYSA-N 0.000 description 2
QUAMTGJKVDWJEQ-UHFFFAOYSA-N octabenzone Chemical compound OC1=CC(OCCCCCCCC)=CC=C1C(=O)C1=CC=CC=C1 QUAMTGJKVDWJEQ-UHFFFAOYSA-N 0.000 description 2
QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 2
229960003921 octisalate Drugs 0.000 description 2
WCJLCOAEJIHPCW-UHFFFAOYSA-N octyl 2-hydroxybenzoate Chemical compound CCCCCCCCOC(=O)C1=CC=CC=C1O WCJLCOAEJIHPCW-UHFFFAOYSA-N 0.000 description 2
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 2
JMANVNJQNLATNU-UHFFFAOYSA-N oxalonitrile Chemical compound N#CC#N JMANVNJQNLATNU-UHFFFAOYSA-N 0.000 description 2
230000035515 penetration Effects 0.000 description 2
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 2
229920003023 plastic Polymers 0.000 description 2
239000004033 plastic Substances 0.000 description 2
150000003254 radicals Chemical class 0.000 description 2
230000004044 response Effects 0.000 description 2
150000003839 salts Chemical class 0.000 description 2
229920002554 vinyl polymer Polymers 0.000 description 2
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230000035483 skin reaction Effects 0.000 description 1
231100000430 skin reaction Toxicity 0.000 description 1
159000000000 sodium salts Chemical class 0.000 description 1
239000007787 solid Substances 0.000 description 1
239000008117 stearic acid Substances 0.000 description 1
125000003696 stearoyl group Chemical group O=C([*])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([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 1
PJANXHGTPQOBST-UHFFFAOYSA-N stilbene Chemical compound C=1C=CC=CC=1C=CC1=CC=CC=C1 PJANXHGTPQOBST-UHFFFAOYSA-N 0.000 description 1
235000021286 stilbenes Nutrition 0.000 description 1
238000007920 subcutaneous administration Methods 0.000 description 1
125000001424 substituent group Chemical group 0.000 description 1
239000004094 surface-active agent Substances 0.000 description 1
230000035900 sweating Effects 0.000 description 1
230000009182 swimming Effects 0.000 description 1
LRBQNJMCXXYXIU-NRMVVENXSA-N tannic acid Chemical compound OC1=C(O)C(O)=CC(C(=O)OC=2C(=C(O)C=C(C=2)C(=O)OC[C@@H]2[C@H]([C@H](OC(=O)C=3C=C(OC(=O)C=4C=C(O)C(O)=C(O)C=4)C(O)=C(O)C=3)[C@@H](OC(=O)C=3C=C(OC(=O)C=4C=C(O)C(O)=C(O)C=4)C(O)=C(O)C=3)[C@@H](OC(=O)C=3C=C(OC(=O)C=4C=C(O)C(O)=C(O)C=4)C(O)=C(O)C=3)O2)OC(=O)C=2C=C(OC(=O)C=3C=C(O)C(O)=C(O)C=3)C(O)=C(O)C=2)O)=C1 LRBQNJMCXXYXIU-NRMVVENXSA-N 0.000 description 1
229940033123 tannic acid Drugs 0.000 description 1
235000015523 tannic acid Nutrition 0.000 description 1
229920002258 tannic acid Polymers 0.000 description 1
208000009056 telangiectasis Diseases 0.000 description 1
239000002562 thickening agent Substances 0.000 description 1
239000004408 titanium dioxide Substances 0.000 description 1
125000003944 tolyl group Chemical group 0.000 description 1
DQFBYFPFKXHELB-VAWYXSNFSA-N trans-chalcone Chemical compound C=1C=CC=CC=1C(=O)\C=C\C1=CC=CC=C1 DQFBYFPFKXHELB-VAWYXSNFSA-N 0.000 description 1
ORHBXUUXSCNDEV-UHFFFAOYSA-N umbelliferone Chemical compound C1=CC(=O)OC2=CC(O)=CC=C21 ORHBXUUXSCNDEV-UHFFFAOYSA-N 0.000 description 1
HFTAFOQKODTIJY-UHFFFAOYSA-N umbelliferone Natural products Cc1cc2C=CC(=O)Oc2cc1OCC=CC(C)(C)O HFTAFOQKODTIJY-UHFFFAOYSA-N 0.000 description 1
239000007762 w/o emulsion Substances 0.000 description 1
238000004383 yellowing Methods 0.000 description 1
239000011787 zinc oxide Substances 0.000 description 1

Landscapes

Cosmetics (AREA)

CA 2029240 1990-11-02 1990-11-02 Compositions de photoprotection ayant une meilleure substantivite Expired - Lifetime CA2029240C (fr)

Priority Applications (1)

Application Number	Priority Date	Filing Date	Title
CA 2029240 CA2029240C (fr)	1990-11-02	1990-11-02	Compositions de photoprotection ayant une meilleure substantivite

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
CA 2029240 CA2029240C (fr)	1990-11-02	1990-11-02	Compositions de photoprotection ayant une meilleure substantivite

Publications (2)

Publication Number	Publication Date
CA2029240A1 CA2029240A1 (fr)	1992-05-03
CA2029240C true CA2029240C (fr)	1998-12-01

Family

ID=4146330

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CA 2029240 Expired - Lifetime CA2029240C (fr)	1990-11-02	1990-11-02	Compositions de photoprotection ayant une meilleure substantivite

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CA (1)	CA2029240C (fr)

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* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US12605314B2 (en)	2018-03-23	2026-04-21	LCS Advanced Solutions, LLC	Broad-spectrum, mineral, photoprotective compositions
US12083199B2 (en)	2019-09-10	2024-09-10	LCS Advanced Solutions, LLC	Mineral, anhydrous, broad-spectrum sunscreen
EP4353328A3 (fr)	2022-10-15	2024-05-22	LCS Advanced Solutions, LLC	Compositions cosmétiques à matrice particulaire de structures diverses, stables et protégeant contre les rayonnements solaires et procédés associés

1990
- 1990-11-02 CA CA 2029240 patent/CA2029240C/fr not_active Expired - Lifetime

Also Published As

Publication number	Publication date
CA2029240A1 (fr)	1992-05-03

Legal Events

Date	Code	Title	Description
1990-11-02	EEER	Examination request
2010-11-02	MKEX	Expiry

Publication	Publication Date	Title
US5219558A (en)	1993-06-15	Photoprotection compositions having improved substantivity
AU705182B2 (en)	1999-05-20	Sunscreen compositions
US5207998A (en)	1993-05-04	Suncare compositions
US5573754A (en)	1996-11-12	Photoprotective compositions
US4919934A (en)	1990-04-24	Cosmetic sticks
US5547659A (en)	1996-08-20	Photoprotection compositions
US5073371A (en)	1991-12-17	Leave-on facial emulsion compositions
US5073372A (en)	1991-12-17	Leave-on facial emulsion compositions
AU692617B2 (en)	1998-06-11	Sunscreen compositions
WO1999062476A1 (fr)	1999-12-09	Composition cosmetique antisolaire
PT100338A (pt)	1993-10-29	Composicoes em emulsao estabilizadas para dar uma tonalidade bronzeada artificial a pele humana que contem dihidroxiacetona e, pelo menos,um alquil fosfato e um copolimero de acido carboc
EP0559786B1 (fr)	1995-07-19	Composition d'emulsion a appliquer sur le visage
CA2029045C (fr)	1995-02-07	Composes de protection contre le rayonnement solaire a efficacite accrue
CA2029240C (fr)	1998-12-01	Compositions de photoprotection ayant une meilleure substantivite
US5516508A (en)	1996-05-14	Photoprotection compositions having improved efficiency
HK1007505B (en)	1999-04-16	Leave-on facial emulsion compositions