LU85746A1 - Composition cosmetique filtrante contenant un filtre uv associe a un polymere obtenu par polymerisation sequentielle en emulsion et son utilisation pour la protection de l'epiderme humain contre les radiations ultraviolettes - Google Patents

Composition cosmetique filtrante contenant un filtre uv associe a un polymere obtenu par polymerisation sequentielle en emulsion et son utilisation pour la protection de l'epiderme humain contre les radiations ultraviolettes Download PDF

Info

Publication number: LU85746A1
Authority: LU; Luxembourg
Prior art keywords: acid; cosmetic; polymer; composition according; filtering composition
Prior art date: 1985-01-28

Application number

LU85746A

Other languages

English (en)

French (fr)

Inventor

Jean-Francois Grollier

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.)

1985-01-28

Filing date

1985-01-28

Publication date

1986-08-04

1985-01-28 Application filed by Oreal filed Critical Oreal

1985-01-28 Priority to LU85746A priority Critical patent/LU85746A1/fr

1986-01-15 Priority to NL8600070A priority patent/NL8600070A/nl

1986-01-23 Priority to CA000500164A priority patent/CA1268424A/fr

1986-01-24 Priority to US06/821,978 priority patent/US4804531A/en

1986-01-27 Priority to CH306/86A priority patent/CH668182A5/fr

1986-01-27 Priority to IT67063/86A priority patent/IT1191989B/it

1986-01-27 Priority to FR8601112A priority patent/FR2576513B1/fr

1986-01-27 Priority to DE19863602353 priority patent/DE3602353A1/de

1986-01-27 Priority to GB08601894A priority patent/GB2170105B/en

1986-01-27 Priority to JP61015569A priority patent/JPS61218514A/ja

1986-01-28 Priority to BE0/216184A priority patent/BE904114A/fr

1986-01-28 Priority to AU52759/86A priority patent/AU602482B2/en

1986-08-04 Publication of LU85746A1 publication Critical patent/LU85746A1/fr

Links

239000000203 mixture Substances 0.000 title claims description 37
239000002537 cosmetic Substances 0.000 title claims description 30
238000001914 filtration Methods 0.000 title claims description 28
229920000642 polymer Polymers 0.000 title claims description 24
238000007720 emulsion polymerization reaction Methods 0.000 title claims description 6
230000005855 radiation Effects 0.000 title description 10
-1 3,4,5-trihydroxybenzoyl Chemical group 0.000 claims description 25
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 12
239000002253 acid Substances 0.000 claims description 11
239000000839 emulsion Substances 0.000 claims description 10
239000004904 UV filter Substances 0.000 claims description 9
239000006185 dispersion Substances 0.000 claims description 9
239000000178 monomer Substances 0.000 claims description 9
239000002245 particle Substances 0.000 claims description 9
DXGLGDHPHMLXJC-UHFFFAOYSA-N oxybenzone Chemical compound OC1=CC(OC)=CC=C1C(=O)C1=CC=CC=C1 DXGLGDHPHMLXJC-UHFFFAOYSA-N 0.000 claims description 7
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 7
NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 6
150000003839 salts Chemical class 0.000 claims description 6
150000001875 compounds Chemical class 0.000 claims description 5
238000000034 method Methods 0.000 claims description 5
239000002304 perfume Substances 0.000 claims description 5
239000000126 substance Substances 0.000 claims description 5
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 4
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 claims description 4
239000002671 adjuvant Substances 0.000 claims description 4
210000002615 epidermis Anatomy 0.000 claims description 4
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 4
230000009477 glass transition Effects 0.000 claims description 4
235000013336 milk Nutrition 0.000 claims description 4
239000008267 milk Substances 0.000 claims description 4
210000004080 milk Anatomy 0.000 claims description 4
238000006386 neutralization reaction Methods 0.000 claims description 4
BCMCBBGGLRIHSE-UHFFFAOYSA-N 1,3-benzoxazole Chemical class C1=CC=C2OC=NC2=C1 BCMCBBGGLRIHSE-UHFFFAOYSA-N 0.000 claims description 3
SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 claims description 3
ALYNCZNDIQEVRV-UHFFFAOYSA-N 4-aminobenzoic acid Chemical compound NC1=CC=C(C(O)=O)C=C1 ALYNCZNDIQEVRV-UHFFFAOYSA-N 0.000 claims description 3
241000723346 Cinnamomum camphora Species 0.000 claims 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 claims description 3
229930008380 camphor Natural products 0.000 claims description 3
238000005253 cladding Methods 0.000 claims description 3
239000006071 cream Substances 0.000 claims description 3
238000004132 cross linking Methods 0.000 claims description 3
UVCJGUGAGLDPAA-UHFFFAOYSA-N ensulizole Chemical compound N1C2=CC(S(=O)(=O)O)=CC=C2N=C1C1=CC=CC=C1 UVCJGUGAGLDPAA-UHFFFAOYSA-N 0.000 claims description 3
239000003755 preservative agent Substances 0.000 claims description 3
210000003491 skin Anatomy 0.000 claims description 3
239000002562 thickening agent Substances 0.000 claims description 3
AFDXODALSZRGIH-QPJJXVBHSA-N (E)-3-(4-methoxyphenyl)prop-2-enoic acid Chemical compound COC1=CC=C(\C=C\C(O)=O)C=C1 AFDXODALSZRGIH-QPJJXVBHSA-N 0.000 claims description 2
239000004909 Moisturizer Substances 0.000 claims description 2
239000000443 aerosol Substances 0.000 claims description 2
229960004050 aminobenzoic acid Drugs 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 description 2
239000000975 dye Substances 0.000 claims description 2
150000002148 esters Chemical class 0.000 claims description 2
JZMJDSHXVKJFKW-UHFFFAOYSA-M methyl sulfate(1-) Chemical compound COS([O-])(=O)=O JZMJDSHXVKJFKW-UHFFFAOYSA-M 0.000 claims description 2
230000001333 moisturizer Effects 0.000 claims description 2
239000002674 ointment Substances 0.000 claims description 2
229960001860 salicylate Drugs 0.000 claims description 2
BBHVQBQNEHFBIO-UHFFFAOYSA-M sodium;2-(3,4-dimethoxyphenyl)-2-oxoacetate Chemical compound [Na+].COC1=CC=C(C(=O)C([O-])=O)C=C1OC BBHVQBQNEHFBIO-UHFFFAOYSA-M 0.000 claims description 2
239000002904 solvent Substances 0.000 claims description 2
230000008961 swelling Effects 0.000 claims description 2
ZNEOHLHCKGUAEB-UHFFFAOYSA-N trimethylphenylammonium Chemical compound C[N+](C)(C)C1=CC=CC=C1 ZNEOHLHCKGUAEB-UHFFFAOYSA-N 0.000 claims description 2
URLKBWYHVLBVBO-UHFFFAOYSA-N Para-Xylene Chemical group CC1=CC=C(C)C=C1 URLKBWYHVLBVBO-UHFFFAOYSA-N 0.000 claims 2
CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 claims 1
239000004480 active ingredient Substances 0.000 claims 1
RWZYAGGXGHYGMB-UHFFFAOYSA-N anthranilic acid Chemical class NC1=CC=CC=C1C(O)=O RWZYAGGXGHYGMB-UHFFFAOYSA-N 0.000 claims 1
WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 claims 1
150000008366 benzophenones Chemical class 0.000 claims 1
125000003354 benzotriazolyl group Chemical class N1N=NC2=C1C=CC=C2* 0.000 claims 1
SESFRYSPDFLNCH-UHFFFAOYSA-N benzyl benzoate Chemical compound C=1C=CC=CC=1C(=O)OCC1=CC=CC=C1 SESFRYSPDFLNCH-UHFFFAOYSA-N 0.000 claims 1
229960002903 benzyl benzoate Drugs 0.000 claims 1
125000000649 benzylidene group Chemical group [H]C(=[*])C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 claims 1
229960000846 camphor Drugs 0.000 claims 1
NZZIMKJIVMHWJC-UHFFFAOYSA-N dibenzoylmethane Chemical class C=1C=CC=CC=1C(=O)CC(=O)C1=CC=CC=C1 NZZIMKJIVMHWJC-UHFFFAOYSA-N 0.000 claims 1
239000003380 propellant Substances 0.000 claims 1
YGSDEFSMJLZEOE-UHFFFAOYSA-M salicylate Chemical compound OC1=CC=CC=C1C([O-])=O YGSDEFSMJLZEOE-UHFFFAOYSA-M 0.000 claims 1
150000003873 salicylate salts Chemical class 0.000 claims 1
JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 claims 1
PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 8
239000003795 chemical substances by application Substances 0.000 description 7
239000001993 wax Substances 0.000 description 7
BXWNKGSJHAJOGX-UHFFFAOYSA-N hexadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCO BXWNKGSJHAJOGX-UHFFFAOYSA-N 0.000 description 6
239000003921 oil Substances 0.000 description 6
235000019198 oils Nutrition 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
239000004166 Lanolin Substances 0.000 description 5
235000019388 lanolin Nutrition 0.000 description 5
229940039717 lanolin Drugs 0.000 description 5
VBICKXHEKHSIBG-UHFFFAOYSA-N 1-monostearoylglycerol Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC(O)CO VBICKXHEKHSIBG-UHFFFAOYSA-N 0.000 description 4
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 4
235000014113 dietary fatty acids Nutrition 0.000 description 4
239000000194 fatty acid Substances 0.000 description 4
229930195729 fatty acid Natural products 0.000 description 4
150000002191 fatty alcohols Chemical class 0.000 description 4
CXVGEDCSTKKODG-UHFFFAOYSA-N sulisobenzone Chemical compound C1=C(S(O)(=O)=O)C(OC)=CC(O)=C1C(=O)C1=CC=CC=C1 CXVGEDCSTKKODG-UHFFFAOYSA-N 0.000 description 4
230000000475 sunscreen effect Effects 0.000 description 4
239000000516 sunscreening agent Substances 0.000 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 description 3
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 3
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
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 3
DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
BLFLLBZGZJTVJG-UHFFFAOYSA-N benzocaine Chemical compound CCOC(=O)C1=CC=C(N)C=C1 BLFLLBZGZJTVJG-UHFFFAOYSA-N 0.000 description 3
229960000541 cetyl alcohol Drugs 0.000 description 3
235000011187 glycerol Nutrition 0.000 description 3
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 3
QUAMTGJKVDWJEQ-UHFFFAOYSA-N octabenzone Chemical compound OC1=CC(OCCCCCCCC)=CC=C1C(=O)C1=CC=CC=C1 QUAMTGJKVDWJEQ-UHFFFAOYSA-N 0.000 description 3
229920002545 silicone oil Polymers 0.000 description 3
OULAJFUGPPVRBK-UHFFFAOYSA-N tetratriacontan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCO OULAJFUGPPVRBK-UHFFFAOYSA-N 0.000 description 3
229940099259 vaseline Drugs 0.000 description 3
PUPZLCDOIYMWBV-UHFFFAOYSA-N (+/-)-1,3-Butanediol Chemical compound CC(O)CCO PUPZLCDOIYMWBV-UHFFFAOYSA-N 0.000 description 2
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
MYRTYDVEIRVNKP-UHFFFAOYSA-N 1,2-Divinylbenzene Chemical compound C=CC1=CC=CC=C1C=C MYRTYDVEIRVNKP-UHFFFAOYSA-N 0.000 description 2
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 2
ZXDDPOHVAMWLBH-UHFFFAOYSA-N 2,4-Dihydroxybenzophenone Chemical compound OC1=CC(O)=CC=C1C(=O)C1=CC=CC=C1 ZXDDPOHVAMWLBH-UHFFFAOYSA-N 0.000 description 2
WSSJONWNBBTCMG-UHFFFAOYSA-N 2-hydroxybenzoic acid (3,3,5-trimethylcyclohexyl) ester Chemical compound C1C(C)(C)CC(C)CC1OC(=O)C1=CC=CC=C1O WSSJONWNBBTCMG-UHFFFAOYSA-N 0.000 description 2
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 2
QQQNPVHFBDPNNA-UHFFFAOYSA-N 3-(3-phenylphenyl)prop-2-enoic acid Chemical compound OC(=O)C=CC1=CC=CC(C=2C=CC=CC=2)=C1 QQQNPVHFBDPNNA-UHFFFAOYSA-N 0.000 description 2
ALYNCZNDIQEVRV-UHFFFAOYSA-M 4-aminobenzoate Chemical compound NC1=CC=C(C([O-])=O)C=C1 ALYNCZNDIQEVRV-UHFFFAOYSA-M 0.000 description 2
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 2
NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 2
DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 2
KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 2
POJWUDADGALRAB-UHFFFAOYSA-N allantoin Chemical compound NC(=O)NC1NC(=O)NC1=O POJWUDADGALRAB-UHFFFAOYSA-N 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
239000010775 animal oil Substances 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
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 2
125000004432 carbon atom Chemical group C* 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
125000002147 dimethylamino group Chemical group [H]C([H])([H])N(*)C([H])([H])[H] 0.000 description 2
MCPKSFINULVDNX-UHFFFAOYSA-N drometrizole Chemical compound CC1=CC=C(O)C(N2N=C3C=CC=CC3=N2)=C1 MCPKSFINULVDNX-UHFFFAOYSA-N 0.000 description 2
230000000694 effects Effects 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
229920000140 heteropolymer Polymers 0.000 description 2
125000005395 methacrylic acid group Chemical group 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
GLDOVTGHNKAZLK-UHFFFAOYSA-N octadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCO GLDOVTGHNKAZLK-UHFFFAOYSA-N 0.000 description 2
AFDXODALSZRGIH-UHFFFAOYSA-N p-coumaric acid methyl ether Natural products COC1=CC=C(C=CC(O)=O)C=C1 AFDXODALSZRGIH-UHFFFAOYSA-N 0.000 description 2
IPCSVZSSVZVIGE-UHFFFAOYSA-N palmitic acid group Chemical group C(CCCCCCCCCCCCCCC)(=O)O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 2
125000000913 palmityl 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])[H] 0.000 description 2
235000019271 petrolatum Nutrition 0.000 description 2
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 2
239000011591 potassium Substances 0.000 description 2
229910052700 potassium Inorganic materials 0.000 description 2
239000011734 sodium Substances 0.000 description 2
229910052708 sodium Inorganic materials 0.000 description 2
150000005846 sugar alcohols Polymers 0.000 description 2
229960000368 sulisobenzone Drugs 0.000 description 2
230000037072 sun protection Effects 0.000 description 2
235000015112 vegetable and seed oil Nutrition 0.000 description 2
239000008158 vegetable oil Substances 0.000 description 2
DTROWQKPZDJELY-UHFFFAOYSA-N (1,2,2-trimethylcyclohexyl) 2-acetamidobenzoate Chemical compound CC(=O)NC1=CC=CC=C1C(=O)OC1(C)C(C)(C)CCCC1 DTROWQKPZDJELY-UHFFFAOYSA-N 0.000 description 1
VMFJVWPCRCAWBS-UHFFFAOYSA-N (3-methoxyphenyl)-phenylmethanone Chemical compound COC1=CC=CC(C(=O)C=2C=CC=CC=2)=C1 VMFJVWPCRCAWBS-UHFFFAOYSA-N 0.000 description 1
GNMDORSUZRRMFS-UHFFFAOYSA-N 1,3-bis(4-methoxyphenyl)propane-1,3-dione Chemical compound C1=CC(OC)=CC=C1C(=O)CC(=O)C1=CC=C(OC)C=C1 GNMDORSUZRRMFS-UHFFFAOYSA-N 0.000 description 1
GDOBGDUGIFUCJV-UHFFFAOYSA-N 2,2-dimethylbutane;2-methylprop-2-enoic acid Chemical compound CCC(C)(C)C.CC(=C)C(O)=O.CC(=C)C(O)=O.CC(=C)C(O)=O GDOBGDUGIFUCJV-UHFFFAOYSA-N 0.000 description 1
IRLYGRLEBKCYPY-UHFFFAOYSA-N 2,5-dimethylbenzenesulfonic acid Chemical compound CC1=CC=C(C)C(S(O)(=O)=O)=C1 IRLYGRLEBKCYPY-UHFFFAOYSA-N 0.000 description 1
RWXMAAYKJDQVTF-UHFFFAOYSA-N 2-(2-hydroxyethoxy)ethyl prop-2-enoate Chemical compound OCCOCCOC(=O)C=C RWXMAAYKJDQVTF-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
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 description 1
CMDKPGRTAQVGFQ-UHFFFAOYSA-N 2-ethoxyethyl 3-(4-methoxyphenyl)prop-2-enoate Chemical compound CCOCCOC(=O)C=CC1=CC=C(OC)C=C1 CMDKPGRTAQVGFQ-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
YTRGIMVXHHFLOY-UHFFFAOYSA-N 2-hydroxypropyl 4-aminobenzoate Chemical compound CC(O)COC(=O)C1=CC=C(N)C=C1 YTRGIMVXHHFLOY-UHFFFAOYSA-N 0.000 description 1
125000002528 4-isopropyl benzyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1C([H])([H])*)C([H])(C([H])([H])[H])C([H])([H])[H] 0.000 description 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 description 1
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241000273930 Brevoortia tyrannus Species 0.000 description 1
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239000002050 international nonproprietary name Substances 0.000 description 1
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GOQYKNQRPGWPLP-UHFFFAOYSA-N n-heptadecyl alcohol Natural products CCCCCCCCCCCCCCCCCO GOQYKNQRPGWPLP-UHFFFAOYSA-N 0.000 description 1
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QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical class CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
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VIKVSUVYUVJHOA-UHFFFAOYSA-N octyl 3-phenylprop-2-enoate Chemical compound CCCCCCCCOC(=O)C=CC1=CC=CC=C1 VIKVSUVYUVJHOA-UHFFFAOYSA-N 0.000 description 1
239000000574 octyl gallate Substances 0.000 description 1
229960001173 oxybenzone Drugs 0.000 description 1
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239000012188 paraffin wax Substances 0.000 description 1
FZUGPQWGEGAKET-UHFFFAOYSA-N parbenate Chemical compound CCOC(=O)C1=CC=C(N(C)C)C=C1 FZUGPQWGEGAKET-UHFFFAOYSA-N 0.000 description 1
235000020232 peanut Nutrition 0.000 description 1
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239000001818 polyoxyethylene sorbitan monostearate Substances 0.000 description 1
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229920001296 polysiloxane Polymers 0.000 description 1
IWHVCHNCTHGORM-UHDJGPCESA-M potassium;(e)-3-phenylprop-2-enoate Chemical compound [K+].[O-]C(=O)\C=C\C1=CC=CC=C1 IWHVCHNCTHGORM-UHDJGPCESA-M 0.000 description 1
238000002360 preparation method Methods 0.000 description 1
230000002335 preservative effect Effects 0.000 description 1
125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
FBCQUCJYYPMKRO-UHFFFAOYSA-N prop-2-enyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCC=C FBCQUCJYYPMKRO-UHFFFAOYSA-N 0.000 description 1
JWCPZKNBPMSYND-UHFFFAOYSA-N propan-2-yl 4-aminobenzoate Chemical compound CC(C)OC(=O)C1=CC=C(N)C=C1 JWCPZKNBPMSYND-UHFFFAOYSA-N 0.000 description 1
WZXKPNYMUZGZIA-RMKNXTFCSA-N propyl (e)-3-(4-methoxyphenyl)prop-2-enoate Chemical compound CCCOC(=O)\C=C\C1=CC=C(OC)C=C1 WZXKPNYMUZGZIA-RMKNXTFCSA-N 0.000 description 1
235000013772 propylene glycol Nutrition 0.000 description 1
150000003902 salicylic acid esters Chemical class 0.000 description 1
229940057910 shea butter Drugs 0.000 description 1
231100000075 skin burn Toxicity 0.000 description 1
239000000600 sorbitol Substances 0.000 description 1
235000010356 sorbitol Nutrition 0.000 description 1
229960002920 sorbitol Drugs 0.000 description 1
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125000004079 stearyl 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])[H] 0.000 description 1
239000001957 sucroglyceride Substances 0.000 description 1
235000010964 sucroglyceride Nutrition 0.000 description 1
229940124530 sulfonamide Drugs 0.000 description 1
150000003456 sulfonamides Chemical class 0.000 description 1
239000003760 tallow Substances 0.000 description 1
TUNFSRHWOTWDNC-UHFFFAOYSA-N tetradecanoic acid Chemical class CCCCCCCCCCCCCC(O)=O TUNFSRHWOTWDNC-UHFFFAOYSA-N 0.000 description 1
WBYWAXJHAXSJNI-VOTSOKGWSA-M trans-cinnamate Chemical compound [O-]C(=O)\C=C\C1=CC=CC=C1 WBYWAXJHAXSJNI-VOTSOKGWSA-M 0.000 description 1
UEVAMYPIMMOEFW-UHFFFAOYSA-N trolamine salicylate Chemical class OCCN(CCO)CCO.OC(=O)C1=CC=CC=C1O UEVAMYPIMMOEFW-UHFFFAOYSA-N 0.000 description 1
XOOUIPVCVHRTMJ-UHFFFAOYSA-L zinc stearate Chemical class [Zn+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O XOOUIPVCVHRTMJ-UHFFFAOYSA-L 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
- A61K8/90—Block copolymers
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q17/00—Barrier preparations; Preparations brought into direct contact with the skin for affording protection against external influences, e.g. sunlight, X-rays or other harmful rays, corrosive materials, bacteria or insect stings
- A61Q17/04—Topical preparations for affording protection against sunlight or other radiation; Topical sun tanning preparations

Landscapes

Health & Medical Sciences (AREA)
Life Sciences & Earth Sciences (AREA)
Animal Behavior & Ethology (AREA)
General Health & Medical Sciences (AREA)
Public Health (AREA)
Veterinary Medicine (AREA)
Dermatology (AREA)
Birds (AREA)
Epidemiology (AREA)
Cosmetics (AREA)

LU85746A 1985-01-28 1985-01-28 Composition cosmetique filtrante contenant un filtre uv associe a un polymere obtenu par polymerisation sequentielle en emulsion et son utilisation pour la protection de l'epiderme humain contre les radiations ultraviolettes LU85746A1 (fr)

Priority Applications (12)

Application Number	Priority Date	Filing Date	Title
LU85746A LU85746A1 (fr)	1985-01-28	1985-01-28	Composition cosmetique filtrante contenant un filtre uv associe a un polymere obtenu par polymerisation sequentielle en emulsion et son utilisation pour la protection de l'epiderme humain contre les radiations ultraviolettes
NL8600070A NL8600070A (nl)	1985-01-28	1986-01-15	Zonnebrandwerend preparaat.
CA000500164A CA1268424A (fr)	1985-01-28	1986-01-23	Composition cosmetique filtrante contenant un filtre uv associe a un polymere obtenu par polymerisation sequentielle en emulsion et son utilisation pour la protection de l'epiderme humain contre les radiations ultraviolettes
US06/821,978 US4804531A (en)	1985-01-28	1986-01-24	Cosmetic screening composition containing a UV screen in combination with a polymer obtained by block polymerization in emulsion and its use for the protection of the human epidermis against ultraviolet radiations
CH306/86A CH668182A5 (fr)	1985-01-28	1986-01-27	Composition cosmetique filtrante contenant un filtre uv associe a un polymere obtenu par polymerisation sequentielle en emulsion.
IT67063/86A IT1191989B (it)	1985-01-28	1986-01-27	Composizione cosmetica filtrante contenente un filtro uv associato ad un polimero ottenuto mediante polimerizzazione sequenziale in emulsione e suo impiego per la protezione dell epidermide umana contro le radiazioni ultraviolette
FR8601112A FR2576513B1 (fr)	1985-01-28	1986-01-27	Composition cosmetique filtrante contenant un filtre uv associe a un polymere obtenu par polymerisation sequentielle en emulsion et son utilisation pour la protection de l'epiderme humain contre les radiations ultraviolettes
DE19863602353 DE3602353A1 (de)	1985-01-28	1986-01-27	Kosmetisches mittel mit uv-filterwirkung und dessen verwendung zum schutz der humanepidermis gegen ultraviolette strahlen
GB08601894A GB2170105B (en)	1985-01-28	1986-01-27	Cosmetic screening composition
JP61015569A JPS61218514A (ja)	1985-01-28	1986-01-27	紫外線吸収化粧品組成物
BE0/216184A BE904114A (fr)	1985-01-28	1986-01-28	Composition cosmetique filtrante contenant un filtre un associe a un polymere obtenu par polymerisation sequentielle en emulsion et son utilisation pour la protection de l'epiderme humain contre les radiations ultraviolettes.
AU52759/86A AU602482B2 (en)	1985-01-28	1986-01-28	Cosmetic screening composition

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
LU85746A LU85746A1 (fr)	1985-01-28	1985-01-28	Composition cosmetique filtrante contenant un filtre uv associe a un polymere obtenu par polymerisation sequentielle en emulsion et son utilisation pour la protection de l'epiderme humain contre les radiations ultraviolettes
LU85746		1985-01-28

Publications (1)

Publication Number	Publication Date
LU85746A1 true LU85746A1 (fr)	1986-08-04

Family

ID=19730396

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
LU85746A LU85746A1 (fr)	1985-01-28	1985-01-28	Composition cosmetique filtrante contenant un filtre uv associe a un polymere obtenu par polymerisation sequentielle en emulsion et son utilisation pour la protection de l'epiderme humain contre les radiations ultraviolettes

Country Status (12)

Country	Link
US (1)	US4804531A (it)
JP (1)	JPS61218514A (it)
AU (1)	AU602482B2 (it)
BE (1)	BE904114A (it)
CA (1)	CA1268424A (it)
CH (1)	CH668182A5 (it)
DE (1)	DE3602353A1 (it)
FR (1)	FR2576513B1 (it)
GB (1)	GB2170105B (it)
IT (1)	IT1191989B (it)
LU (1)	LU85746A1 (it)
NL (1)	NL8600070A (it)

Families Citing this family (38)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JPS61215309A (ja) *	1985-03-20	1986-09-25	Shiseido Co Ltd	皮膚外用剤
JPS6354310A (ja) *	1986-07-18	1988-03-08	ミネソタ　マイニング　アンド　マニユフアクチユアリング　カンパニ−	ポリマ−で増粘した油状マクロ・カプセルを含む化粧品に有用なカプセル化オイルのマイクロカプセル
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
LU86762A1 (fr) *	1987-02-06	1988-11-17	Oreal	Composition cosmetique filtrante sous forme d'emulsion huile-dans-l'eau comprenant un filtre uv-a et un filtre uv-b et son utilisation pour la protection de la peau contre les radiations ultraviolettes
US5240695A (en) *	1988-02-11	1993-08-31	L'oreal	Use of 2-hydroxy-4-methoxybenzophenone-5-sulphonic acid or its salts for protecting the hair against environmental attacking agents, and especially against light and process for protecting the hair using the compound
US5275810A (en) *	1988-02-25	1994-01-04	L'oreal	Cosmetic composition for maintaining the hairstyle containing an oxazoline polymer and a 2-hydroxy-4-methoxy-benzophenone-5-sulphonic acid, salified or otherwise
FR2628319B1 (fr) *	1988-03-09	1990-12-07	Oreal	Compositions pharmaceutiques et cosmetiques a base de peroxyde de benzoyle et de sels d'ammonium quaternaires
AT393451B (de) *	1988-03-23	1991-10-25	Biogal Gyogyszergyar	Kosmetisches lichtschutzpraeparat und verfahren zu seiner herstellung
FR2636530B1 (fr) *	1988-08-24	1992-05-07	Oreal	Composition cosmetique filtrante photostable sous forme d'emulsion contenant un filtre hydrosoluble a large bande d'absorption et au moins un filtre uv-a liposoluble et son utilisation pour la protection de la peau contre le rayonnement ultraviolet
CA2029045C (en) *	1989-11-29	1995-02-07	Lauren Ann Thaman	Photoprotection compositions having improved efficiency
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.
US5223250A (en) *	1991-02-05	1993-06-29	Sun Smart, Inc.	Visibly transparent UV sunblock cosmetic compositions
US5733531A (en) *	1991-02-05	1998-03-31	Sunsmart, Inc.	Composite UV sunblock compositions
AU668862B2 (en) *	1991-02-05	1996-05-23	Basf Corporation	Visibly transparent UV sunblock agents and methods of making same
GB9211708D0 (en) †	1992-06-03	1992-07-15	Unilever Plc	Cosmetic composition
CA2142298A1 (en) *	1992-08-13	1994-03-03	George E. Deckner	Photostable sunscreen compositions
FR2714827B1 (fr) *	1994-01-10	1996-03-22	Oreal	Composition cosmétique ou dermatologique contenant un pseudo-latex constitué de particules d'un homopolymère-filtre U.V..
EP0669124A1 (en) *	1994-02-28	1995-08-30	Rohm And Haas Company	Ultraviolet radiation absorbing composition
US5663213A (en) *	1994-02-28	1997-09-02	Rohm And Haas Company	Method of improving ultraviolet radiation absorption of a composition
FR2727113B1 (fr) *	1994-11-17	1996-12-27	Oreal	Nouveaux filtres solaires, compositions cosmetiques photoprotectrices les contenant et utilisations
US5716554A (en) *	1995-02-21	1998-02-10	Shiseido Co., Ltd.	Ultraviolet light absorbent
FR2742049B1 (fr) *	1995-12-12	1998-02-27	Rocher Yves Biolog Vegetale	Melange comprenant des extraits vegetaux pour l'hydratation des couches superieures de l'epiderme
US5770183A (en) *	1996-08-01	1998-06-23	Linares; Francisco J.	High SPF (30 and over) waterproof sunblock compositions
US5744062A (en) *	1996-08-29	1998-04-28	R.I.T.A. Corporation	Balanced emulsifier blends for oil-in-water emulsions
US6720141B1 (en) *	1999-11-01	2004-04-13	Interleukin Genetics, Inc.	Diagnostics and therapeutics for restenosis
GB9715751D0 (en) *	1997-07-26	1997-10-01	Ciba Geigy Ag	Formulations
US5985251A (en) *	1997-12-01	1999-11-16	Roche Vitamins Inc.	Light screening compositions
US6007797A (en) *	1998-08-06	1999-12-28	Ipa, Llc	Disappearing color sunscreen compositions
CA2322345A1 (en) *	1999-10-14	2001-04-14	Rohm And Haas Company	Method for preparing ultraviolet radiation-absorbing compositions
FR2850277B1 (fr) *	2003-01-24	2005-04-08	Lanatech	Composition comprenant un extrait d'aphanizomenon flos-aquae, son utilisation et sa preparation
FR2853534B1 (fr) *	2003-04-14	2006-06-23	Oreal	Composition photoprotectrice aqueuse comprenant au moins un copolymere diblocs ou triblocs et un 4,4-diarylbutadiene, utilisations
AU2003903838A0 (en)	2003-07-23	2003-08-07	Orica Australia Pty Ltd	Aqueous polymer dispersion
KR101557973B1 (ko) *	2007-04-13	2015-10-08	한국생명공학연구원	자외선 차단물질을 함유하는 고분자 나노입자 및 그제조방법
BRPI0816217A2 (pt) *	2007-09-06	2015-06-16	Hallstar Innovations Corp	Fluidos de silicone fotoestabilizantes
US7964245B2 (en) *	2008-06-27	2011-06-21	Hallstar Innovations Corp.	UV-absorbing and photostabilizing polymers
US10512601B2 (en)	2014-12-18	2019-12-24	L'oréal	Compositions having improved water resistance
WO2016100815A1 (en) *	2014-12-18	2016-06-23	L'oreal	Compositions having improved spf and/or water resistance

Family Cites Families (11)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US2628205A (en) *	1950-10-21	1953-02-10	Res Prod Corp	Viscous hydrophilic composition and method of making the same
CA1091161A (en) *	1975-12-03	1980-12-09	James A. Mezick	Oil in water emulsion film forming sunscreen compositions
GB1579934A (en) *	1976-10-14	1980-11-26	Beecham Group Ltd	Skin-care cosmetic products
LU78001A1 (fr) *	1977-08-22	1979-05-23	Oreal	Nouvelles compositions cosmetiques sous forme d'emulsions eau-dans-l'huile ou huile-dans-l'eau
AU528642B2 (en) *	1978-07-19	1983-05-05	Charles Of The Ritz Group Ltd.	Sunblock formulation
IT1164522B (it) *	1978-11-21	1987-04-15	Elf Aquitaine	Polimeri organici a gruppi attivi,particolarmente per pigmenti,vernici,cosmetici ed altri impieghi
CA1180474A (en) *	1979-06-26	1985-01-02	Alexander Kowalski	Sequential heteropolymer dispersion and a particulate material obtainable therefrom useful in coating compositions as a thickening and/or opacifying agent
US4522808A (en) *	1980-08-15	1985-06-11	Societe Anonyme Dite: L'oreal	Anti-sunburn compositions containing 2-phenyl-indole derivatives
JPS57123112A (en) *	1980-12-30	1982-07-31	Union Carbide Corp	Effect increase of local composition
US4524061A (en) *	1983-04-22	1985-06-18	Gaf Corporation	Polymeric sunscreens
FR2549842B1 (fr) *	1983-07-25	1988-01-29	Oreal	Copolymeres d'acide acrylique ou methacrylique, d'un acrylate ou methacrylate d'alkyle et d'un derive allylique, et leur utilisation en cosmetique

1985
- 1985-01-28 LU LU85746A patent/LU85746A1/fr unknown
1986
- 1986-01-15 NL NL8600070A patent/NL8600070A/nl not_active Application Discontinuation
- 1986-01-23 CA CA000500164A patent/CA1268424A/fr not_active Expired - Lifetime
- 1986-01-24 US US06/821,978 patent/US4804531A/en not_active Expired - Fee Related
- 1986-01-27 IT IT67063/86A patent/IT1191989B/it active
- 1986-01-27 DE DE19863602353 patent/DE3602353A1/de not_active Withdrawn
- 1986-01-27 FR FR8601112A patent/FR2576513B1/fr not_active Expired
- 1986-01-27 GB GB08601894A patent/GB2170105B/en not_active Expired
- 1986-01-27 JP JP61015569A patent/JPS61218514A/ja active Pending
- 1986-01-27 CH CH306/86A patent/CH668182A5/fr not_active IP Right Cessation
- 1986-01-28 AU AU52759/86A patent/AU602482B2/en not_active Ceased
- 1986-01-28 BE BE0/216184A patent/BE904114A/fr not_active IP Right Cessation

Also Published As

Publication number	Publication date
GB8601894D0 (en)	1986-03-05
US4804531A (en)	1989-02-14
GB2170105A (en)	1986-07-30
JPS61218514A (ja)	1986-09-29
IT1191989B (it)	1988-03-31
BE904114A (fr)	1986-07-28
AU602482B2 (en)	1990-10-18
DE3602353A1 (de)	1986-07-31
AU5275986A (en)	1986-07-31
CH668182A5 (fr)	1988-12-15
FR2576513A1 (fr)	1986-08-01
IT8667063A0 (it)	1986-01-27
NL8600070A (nl)	1986-08-18
FR2576513B1 (fr)	1988-05-13
GB2170105B (en)	1989-01-11
CA1268424A (fr)	1990-05-01

Publication	Publication Date	Title
CA1268424A (fr)	1990-05-01	Composition cosmetique filtrante contenant un filtre uv associe a un polymere obtenu par polymerisation sequentielle en emulsion et son utilisation pour la protection de l'epiderme humain contre les radiations ultraviolettes
EP0518772B1 (fr)	1994-11-02	Composition cosmétique filtrante contenant un mélange d'acide benzène 1,4-di(3-méthylidène-10-camphosulfonique) partiellement ou totalement neutralisé et de nanopigments d'oxydes métalliques
EP0966954B1 (fr)	2002-02-20	Compositions cosmétiques photoprotectrices, contenant un nanopigment d'oxyde métallique et un terpolymère acrylique et utilisation de ces compositions pour protéger les matières kératiniques contre le rayonnement ultraviolet
EP0685222B1 (fr)	1996-09-11	Compositions cosmétiques photoprotectrices et utilisations
BE1004752A3 (fr)	1993-01-26	Composition cosmetique transparente reflechissant le rayonnement infrarouge a base de flocons de dioxyde de titane et son utilisation pour la protection de l'epiderme humain contre le rayonnement infrarouge.
CA2150869C (fr)	2001-08-14	Composition cosmetique anti uv a base de 2,4,6-tris¬p-(2'ethylhexyl-l'oxycarbonyl)anilino\|-1,3,5-triazine sous forme solubilisee par le salicylate d'homomenthyle et/ou le salicylate d'octyle
CA1265060A (fr)	1990-01-30	Composition solaire filtrante contenant du polyisobutylene et son utilisation pour la protection de l'epiderme humain contre les radiations ultraviolettes
BE1000405A3 (fr)	1988-11-22	Composition cosmetique photostable contenant un derive d'ethylrutine a titre d'agent de protection contre la lumiere solaire et son utilisation pour la protection de la peau et des cheveux.
FR2718638A1 (fr)	1995-10-20	Compositions cosmétiques filtrantes contenant un agent hydrophile acide et utilisation.
FR2720632A1 (fr)	1995-12-08	Compositions cosmétiques photoprotectrices contenant un système filtrant les rayons UV et des polymères particuliers et utilisations.
FR2562796A1 (fr)	1985-10-18	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
EP0685221B1 (fr)	1999-06-30	Compositions cosmétiques photoprotectrices à base d'un mélange synergétique de filtres et utilisations
EP0293579B1 (fr)	1991-04-10	Compositions cosmétiques contenant un complexe cuivrique de l'acide 3,5-diisopropyl salicylique pour la protection contre le rayonnement UV et utilisation d'un tel composé en cosmétique
EP1096916B1 (fr)	2009-08-19	Procede de photostabilisation de derives du dibenzoylmethane
FR2720638A1 (fr)	1995-12-08	Compositions cosmétiques antisolaires à base d'un mélange synergétique de filtres et utilisations.
EP0865271B1 (fr)	2000-01-19	Compositions de protection solaires stabilisees
FR2858554A1 (fr)	2005-02-11	Emulsions solaires a phase externe huileuse
FR2751217A1 (fr)	1998-01-23	Utilisation de l'iodo-3 propynyl-2 butylcarbamate dans une composition cosmetique et/ou dermatologique comme actif pour le traitement de la seborrhee