AU2004224086B2 - Symmetrical triazine derivatives - Google Patents
Symmetrical triazine derivatives Download PDFInfo
- Publication number
- AU2004224086B2 AU2004224086B2 AU2004224086A AU2004224086A AU2004224086B2 AU 2004224086 B2 AU2004224086 B2 AU 2004224086B2 AU 2004224086 A AU2004224086 A AU 2004224086A AU 2004224086 A AU2004224086 A AU 2004224086A AU 2004224086 B2 AU2004224086 B2 AU 2004224086B2
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- Australia
- Prior art keywords
- formula
- cosmetic preparation
- radical
- filter combination
- preparation according
- Prior art date
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- 150000003918 triazines Chemical class 0.000 title claims description 44
- 150000001875 compounds Chemical class 0.000 claims description 106
- 238000002360 preparation method Methods 0.000 claims description 64
- 239000004904 UV filter Substances 0.000 claims description 51
- 239000002537 cosmetic Substances 0.000 claims description 41
- -1 hydroxyphenyltriazine compound Chemical class 0.000 claims description 40
- 239000000203 mixture Substances 0.000 claims description 33
- 229910052739 hydrogen Inorganic materials 0.000 claims description 32
- 239000001257 hydrogen Substances 0.000 claims description 30
- 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 26
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 23
- 125000000217 alkyl group Chemical group 0.000 claims description 13
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 claims description 8
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 8
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 8
- 102100028572 Disabled homolog 2 Human genes 0.000 claims description 6
- 101710197163 Disabled homolog 2 Proteins 0.000 claims description 6
- 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 6
- 239000002671 adjuvant Substances 0.000 claims description 5
- 150000002148 esters Chemical class 0.000 claims description 5
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 5
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 5
- FMJSMJQBSVNSBF-UHFFFAOYSA-N octocrylene Chemical compound C=1C=CC=CC=1C(=C(C#N)C(=O)OCC(CC)CCCC)C1=CC=CC=C1 FMJSMJQBSVNSBF-UHFFFAOYSA-N 0.000 claims description 5
- 229920001296 polysiloxane Polymers 0.000 claims description 5
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 5
- 150000003839 salts Chemical class 0.000 claims description 5
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 claims description 5
- 239000005711 Benzoic acid Substances 0.000 claims description 4
- 229910001413 alkali metal ion Inorganic materials 0.000 claims description 4
- 125000003545 alkoxy group Chemical group 0.000 claims description 4
- 235000010233 benzoic acid Nutrition 0.000 claims description 4
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 claims description 4
- HUVYTMDMDZRHBN-UHFFFAOYSA-N drometrizole trisiloxane Chemical compound C[Si](C)(C)O[Si](C)(O[Si](C)(C)C)CC(C)CC1=CC(C)=CC(N2N=C3C=CC=CC3=N2)=C1O HUVYTMDMDZRHBN-UHFFFAOYSA-N 0.000 claims description 4
- 229910052751 metal Inorganic materials 0.000 claims description 4
- 239000002184 metal Substances 0.000 claims description 4
- MAOBFOXLCJIFLV-UHFFFAOYSA-N (2-aminophenyl)-phenylmethanone Chemical class NC1=CC=CC=C1C(=O)C1=CC=CC=C1 MAOBFOXLCJIFLV-UHFFFAOYSA-N 0.000 claims description 3
- 239000007983 Tris buffer Substances 0.000 claims description 3
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- 239000000969 carrier Substances 0.000 claims description 3
- 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 3
- GLCJMPWWQKKJQZ-UHFFFAOYSA-L disodium;2-[4-(4,6-disulfonato-1h-benzimidazol-2-yl)phenyl]-1h-benzimidazole-4,6-disulfonate;hydron Chemical compound [Na+].[Na+].C1=C(S(O)(=O)=O)C=C2NC(C3=CC=C(C=C3)C3=NC4=C(C=C(C=C4N3)S(=O)(=O)O)S([O-])(=O)=O)=NC2=C1S([O-])(=O)=O GLCJMPWWQKKJQZ-UHFFFAOYSA-L 0.000 claims description 3
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims description 3
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims description 3
- 125000002373 5 membered heterocyclic group Chemical group 0.000 claims description 2
- 125000004070 6 membered heterocyclic group Chemical group 0.000 claims description 2
- 125000004450 alkenylene group Chemical group 0.000 claims description 2
- 125000002947 alkylene group Chemical group 0.000 claims description 2
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims description 2
- 125000005708 carbonyloxy group Chemical group [*:2]OC([*:1])=O 0.000 claims description 2
- 150000001768 cations Chemical class 0.000 claims description 2
- 125000002993 cycloalkylene group Chemical group 0.000 claims description 2
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims description 2
- 125000004433 nitrogen atom Chemical group N* 0.000 claims description 2
- 229920006395 saturated elastomer Polymers 0.000 claims description 2
- YVNNUPPJVSXCTF-UHFFFAOYSA-L trimethyl-[2-methyl-4-[(4,7,7-trimethyl-3-oxo-2-bicyclo[2.2.1]heptanylidene)methyl]phenyl]azanium;sulfate Chemical compound [O-]S([O-])(=O)=O.C1=C([N+](C)(C)C)C(C)=CC(C=C2C(C3(CCC2C3(C)C)C)=O)=C1.C1=C([N+](C)(C)C)C(C)=CC(C=C2C(C3(CCC2C3(C)C)C)=O)=C1 YVNNUPPJVSXCTF-UHFFFAOYSA-L 0.000 claims description 2
- CATSNJVOTSVZJV-UHFFFAOYSA-N heptan-2-one Chemical compound CCCCCC(C)=O CATSNJVOTSVZJV-UHFFFAOYSA-N 0.000 claims 2
- 125000000325 methylidene group Chemical group [H]C([H])=* 0.000 claims 2
- KPPVNWGJXFMGAM-UUILKARUSA-N (e)-2-methyl-1-(6-methyl-3,4-dihydro-2h-quinolin-1-yl)but-2-en-1-one Chemical compound CC1=CC=C2N(C(=O)C(/C)=C/C)CCCC2=C1 KPPVNWGJXFMGAM-UUILKARUSA-N 0.000 claims 1
- 125000000590 4-methylphenyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)C([H])([H])[H] 0.000 claims 1
- KPUWHANPEXNPJT-UHFFFAOYSA-N disiloxane Chemical class [SiH3]O[SiH3] KPUWHANPEXNPJT-UHFFFAOYSA-N 0.000 claims 1
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- 238000003756 stirring Methods 0.000 description 38
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- LXCFILQKKLGQFO-UHFFFAOYSA-N methylparaben Chemical compound COC(=O)C1=CC=C(O)C=C1 LXCFILQKKLGQFO-UHFFFAOYSA-N 0.000 description 34
- QELSKZZBTMNZEB-UHFFFAOYSA-N propylparaben Chemical compound CCCOC(=O)C1=CC=C(O)C=C1 QELSKZZBTMNZEB-UHFFFAOYSA-N 0.000 description 32
- QFOHBWFCKVYLES-UHFFFAOYSA-N Butylparaben Chemical compound CCCCOC(=O)C1=CC=C(O)C=C1 QFOHBWFCKVYLES-UHFFFAOYSA-N 0.000 description 28
- 239000006185 dispersion Substances 0.000 description 28
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 27
- 229920001577 copolymer Polymers 0.000 description 27
- GLDOVTGHNKAZLK-UHFFFAOYSA-N octadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCO GLDOVTGHNKAZLK-UHFFFAOYSA-N 0.000 description 27
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- 238000001816 cooling Methods 0.000 description 24
- 229960001679 octinoxate Drugs 0.000 description 23
- BXWNKGSJHAJOGX-UHFFFAOYSA-N hexadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCO BXWNKGSJHAJOGX-UHFFFAOYSA-N 0.000 description 22
- 238000004519 manufacturing process Methods 0.000 description 22
- 150000003254 radicals Chemical class 0.000 description 22
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- BANXPJUEBPWEOT-UHFFFAOYSA-N 2-methyl-Pentadecane Chemical compound CCCCCCCCCCCCCC(C)C BANXPJUEBPWEOT-UHFFFAOYSA-N 0.000 description 20
- 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 18
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- 229940008099 dimethicone Drugs 0.000 description 17
- 239000004205 dimethyl polysiloxane Substances 0.000 description 17
- 239000003205 fragrance Substances 0.000 description 17
- 235000010270 methyl p-hydroxybenzoate Nutrition 0.000 description 17
- 239000004292 methyl p-hydroxybenzoate Substances 0.000 description 17
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- 229940067596 butylparaben Drugs 0.000 description 14
- 229960001617 ethyl hydroxybenzoate Drugs 0.000 description 14
- 235000010228 ethyl p-hydroxybenzoate Nutrition 0.000 description 14
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- NUVBSKCKDOMJSU-UHFFFAOYSA-N ethylparaben Chemical compound CCOC(=O)C1=CC=C(O)C=C1 NUVBSKCKDOMJSU-UHFFFAOYSA-N 0.000 description 14
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- ZUOUZKKEUPVFJK-UHFFFAOYSA-N diphenyl Chemical group C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 12
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- FJKROLUGYXJWQN-UHFFFAOYSA-N papa-hydroxy-benzoic acid Natural products OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 description 1
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- MILWSGRFEGYSGM-UHFFFAOYSA-N propane-1,2-diol;propane-1,2,3-triol Chemical compound CC(O)CO.OCC(O)CO MILWSGRFEGYSGM-UHFFFAOYSA-N 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
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- 239000002437 shaving preparation Substances 0.000 description 1
- LIVNPJMFVYWSIS-UHFFFAOYSA-N silicon monoxide Inorganic materials [Si-]#[O+] LIVNPJMFVYWSIS-UHFFFAOYSA-N 0.000 description 1
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- IWIUXJGIDSGWDN-UQKRIMTDSA-M sodium;(2s)-2-(dodecanoylamino)pentanedioate;hydron Chemical compound [Na+].CCCCCCCCCCCC(=O)N[C@H](C([O-])=O)CCC(O)=O IWIUXJGIDSGWDN-UQKRIMTDSA-M 0.000 description 1
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- 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 1
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- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 1
- DZKXJUASMGQEMA-UHFFFAOYSA-N tetradecyl tetradecanoate Chemical compound CCCCCCCCCCCCCCOC(=O)CCCCCCCCCCCCC DZKXJUASMGQEMA-UHFFFAOYSA-N 0.000 description 1
- 230000001225 therapeutic effect Effects 0.000 description 1
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- 235000015961 tonic Nutrition 0.000 description 1
- 230000001256 tonic effect Effects 0.000 description 1
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- LOIYMIARKYCTBW-OWOJBTEDSA-N trans-urocanic acid Chemical compound OC(=O)\C=C\C1=CNC=N1 LOIYMIARKYCTBW-OWOJBTEDSA-N 0.000 description 1
- 150000003626 triacylglycerols Chemical class 0.000 description 1
- 238000005829 trimerization reaction Methods 0.000 description 1
- LINXHFKHZLOLEI-UHFFFAOYSA-N trimethyl-[phenyl-bis(trimethylsilyloxy)silyl]oxysilane Chemical compound C[Si](C)(C)O[Si](O[Si](C)(C)C)(O[Si](C)(C)C)C1=CC=CC=C1 LINXHFKHZLOLEI-UHFFFAOYSA-N 0.000 description 1
- GETQZCLCWQTVFV-UHFFFAOYSA-N trimethylamine Chemical compound CN(C)C GETQZCLCWQTVFV-UHFFFAOYSA-N 0.000 description 1
- 125000000026 trimethylsilyl group Chemical group [H]C([H])([H])[Si]([*])(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
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Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/49—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D251/00—Heterocyclic compounds containing 1,3,5-triazine rings
- C07D251/02—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings
- C07D251/12—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members
- C07D251/14—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members with hydrogen or carbon atoms directly attached to at least one ring carbon atom
- C07D251/24—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members with hydrogen or carbon atoms directly attached to at least one ring carbon atom to three ring carbon atoms
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/49—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds
- A61K8/494—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds with more than one nitrogen as the only hetero atom
- A61K8/4966—Triazines or their condensed derivatives
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q17/00—Barrier preparations; Preparations brought into direct contact with the skin for affording protection against external influences, e.g. sunlight, X-rays or other harmful rays, corrosive materials, bacteria or insect stings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q17/00—Barrier preparations; Preparations brought into direct contact with the skin for affording protection against external influences, e.g. sunlight, X-rays or other harmful rays, corrosive materials, bacteria or insect stings
- A61Q17/04—Topical preparations for affording protection against sunlight or other radiation; Topical sun tanning preparations
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- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Dermatology (AREA)
- Birds (AREA)
- Epidemiology (AREA)
- Cosmetics (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP03100758 | 2003-03-24 | ||
| EP03100758.6 | 2003-03-24 | ||
| EP03102325 | 2003-07-29 | ||
| EP03102325.2 | 2003-07-29 | ||
| PCT/EP2004/050331 WO2004085412A2 (en) | 2003-03-24 | 2004-03-19 | Symmetrical triazine derivatives |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| AU2004224086A1 AU2004224086A1 (en) | 2004-10-07 |
| AU2004224086B2 true AU2004224086B2 (en) | 2011-02-10 |
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| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AU2004224086A Expired AU2004224086B2 (en) | 2003-03-24 | 2004-03-19 | Symmetrical triazine derivatives |
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| Country | Link |
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| US (1) | US7311897B2 (enExample) |
| EP (1) | EP1606270B1 (enExample) |
| JP (1) | JP4764817B2 (enExample) |
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| AU (1) | AU2004224086B2 (enExample) |
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| MX (1) | MX267068B (enExample) |
| TW (1) | TWI331997B (enExample) |
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| US10292922B2 (en) | 2015-12-31 | 2019-05-21 | L'oreal | Silicone-wax dispersion compositions for removing cosmetic films |
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| FR3060361B1 (fr) | 2016-12-21 | 2018-12-07 | L'oreal | Emulsion eau-dans-huile comprenant un systeme emulsionnant particulier, une argile lipophile, une poudre d’organopolysiloxane elastomerique enrobee d’une resine de silicone |
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| FR3060997B1 (fr) | 2016-12-23 | 2019-05-31 | L'oreal | Composition comprenant de la baicaline |
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| FR3073408B1 (fr) | 2017-11-15 | 2019-10-11 | L'oreal | Compositions comprenant au moins un polymere acrylique et au moins un filtre organique insoluble |
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| FR3073409B1 (fr) | 2017-11-15 | 2019-10-11 | L'oreal | Composition cosmetique ou dermatologique comprenant une merocyanine et un polymere acrylique. |
| FR3073400B1 (fr) | 2017-11-15 | 2024-08-09 | Oreal | Emulsion cosmetique contenant un tensioactif gemine et un polymere lipophile |
| WO2019119078A1 (en) | 2017-12-19 | 2019-06-27 | L'oreal | Sun care composition |
| FR3075050B1 (fr) | 2017-12-19 | 2020-01-03 | L'oreal | Composition comprenant de la baicaline et un compose antioxydant |
| WO2019119077A1 (en) | 2017-12-19 | 2019-06-27 | L'oreal | Sun care composition |
| FR3075630B1 (fr) * | 2017-12-22 | 2020-11-06 | Lvmh Rech | Emulsion huile-dans-eau pour le maquillage et le soin des levres |
| CN112105704B (zh) * | 2018-03-30 | 2023-08-22 | 株式会社艾迪科 | 颗粒状紫外线吸收剂和树脂组合物 |
| JP6837148B2 (ja) * | 2018-03-30 | 2021-03-03 | 株式会社Adeka | 粒状紫外線吸収剤および樹脂組成物 |
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| FR3083097B1 (fr) | 2018-06-28 | 2020-11-27 | Oreal | Composition cosmetique ou dermatologique comprenant une merocyanine et une phase huileuse comprenant au moins un carbonate d’alkyle ou d’alkylene |
| WO2020000068A1 (en) | 2018-06-28 | 2020-01-02 | L'oreal | Surfactant system and sunscreen composition comprising it |
| FR3083093A1 (fr) | 2018-06-28 | 2020-01-03 | L'oreal | Composition photoprotectrice comprenant des particules de silice colloidale |
| FR3083118B1 (fr) | 2018-07-02 | 2021-01-08 | Lvmh Rech | Composition gelifiee avec filtres uv |
| BR112020024706B1 (pt) | 2018-07-31 | 2023-04-04 | L'oreal | Composição de proteção solar, uso de uma composição e processo de fabricação de uma composição |
| BR112021001607B1 (pt) | 2018-07-31 | 2023-04-04 | L'oreal | Composição de protetor solar e uso da composição de protetor solar |
| WO2020109264A1 (en) * | 2018-11-26 | 2020-06-04 | Dsm Ip Assets B.V. | Cosmetic composition comprising specific hyperbranched copolymers and anionic emulsifiers |
| FR3090329B1 (fr) | 2018-12-21 | 2020-12-04 | Oreal | Composition comprenant un filtre UV, un polymère hydrophile réticulé anionique, un tensioactif ayant une HLB inférieure ou égale à 5 et un alcane non volatil |
| FR3090337B1 (fr) | 2018-12-21 | 2021-10-29 | Oreal | Composition photoprotectrice fluide |
| WO2020163928A1 (en) | 2019-02-13 | 2020-08-20 | L'oreal | Sunscreen composition, use of the sunscreen composition and process of manufacturing the sunscreen composition |
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| WO2021016684A1 (en) | 2019-07-31 | 2021-02-04 | L'oreal | Cosmetic composition, process for manufacturing the cosmetic composition and its use |
| CN110624388B (zh) * | 2019-10-28 | 2022-04-15 | 深圳市爱康泉水处理服务有限公司 | 除臭组合物、除臭剂及其应用 |
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| FR3103704B1 (fr) | 2019-11-29 | 2022-07-08 | Oreal | Composition comprenant un filtre UV, un polymère éthylénique à groupe acide phosphonique et une huile hydrocarbonée |
| KR102861240B1 (ko) | 2020-06-30 | 2025-09-18 | 로레알 | 화장용 선스크린 조성물, 화장용 선스크린 조성물의 용도, 및 화장용 선스크린 조성물의 제조 방법 |
| FR3115457B1 (fr) | 2020-10-23 | 2022-10-21 | Oreal | Composition photoprotectrice |
| FR3117824A1 (fr) | 2020-12-18 | 2022-06-24 | L'oreal | Composition cosmétique ou dermatologique comprenant une mérocyanine et une phase huileuse comprenant au moins un ester d’acide citrique |
| WO2022160020A1 (en) | 2021-01-29 | 2022-08-04 | L'oreal | Water-in-oil cosmetic sunscreen composition, use of a water-in-oil cosmetic sunscreen composition, and process for manufacturing a water-in-oil cosmetic sunscreen composition |
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| CN114028276B (zh) * | 2021-12-17 | 2023-09-26 | 上海蜂花日用品有限公司 | 一种具有多效修护效果的护发组合物及其应用 |
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| FR3138306A1 (fr) | 2022-07-26 | 2024-02-02 | L'oreal | Composition comprenant un filtre UV, un polymère superabsorbant et un phospholipide |
| WO2024083567A1 (en) | 2022-10-21 | 2024-04-25 | L'oreal | Composition comprising a lipophilic organic screening agent, a hydrophilic organic screening agent, with an amount by weight of fatty phase between 20 and 70% |
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| FR3141060A1 (fr) | 2022-10-21 | 2024-04-26 | L'oreal | Composition comprenant un filtre UV organique lipophile, un filtre UV organique hydrophile et un polymère gélifiant hydrophile spécifique |
| FR3141062A1 (fr) | 2022-10-21 | 2024-04-26 | L'oreal | Composition comprenant un filtre organique lipophile, un filtre organique hydrophile, avec une quantité en poids de phase grasse entre 20 et 70 % et un ratio massique filtres organiques hydrophiles / filtres organiques lipophiles supérieur à 0,3 |
| FR3142897A1 (fr) | 2022-12-09 | 2024-06-14 | L'oreal | Composition comprenant un filtre organique hydrodispersible et au moins un complexe polyionique contenant un polysaccharide cationique et un acide non polymérique ayant au moins 3 valeurs de pKa et/ou l’un de ses sels |
| WO2024124309A1 (en) | 2022-12-12 | 2024-06-20 | L'oreal | Cosmetic sunscreen composition and its use |
| WO2024124310A1 (en) | 2022-12-12 | 2024-06-20 | L'oreal | Cosmetic sunscreen composition and its use |
| FR3143344A1 (fr) | 2022-12-16 | 2024-06-21 | L'oreal | Composition comprenant un filtre UV, un polymère lipophile convenablement sélectionné, et un carraghénane |
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| WO2024160671A1 (en) | 2023-01-30 | 2024-08-08 | Basf Se | Composition comprising 1,3,5-triazine, 2,4,6-tris[1,1'-biphenyl]-4-yl with lower amounts of impurities |
| CN120548166A (zh) | 2023-01-30 | 2025-08-26 | 巴斯夫欧洲公司 | 包含具有较低杂质量的1,3,5-三嗪, 2,4,6-三[1,1’-联苯]-4-基的组合物 |
| FR3149786A1 (fr) | 2023-06-16 | 2024-12-20 | L'oreal | Composition comprenant un filtre UV, un polymère semi-cristallin contenant au moins une chaine d’alkyl acrylate et une gomme de scléroglucane |
| FR3149779A1 (fr) | 2023-06-16 | 2024-12-20 | L'oreal | Composition comprenant un filtre UV, au moins 1 % en poids d’acide ascorbique et une gomme de scléroglucane |
| FR3149777A1 (fr) | 2023-06-16 | 2024-12-20 | L'oreal | Composition cosmétique ou dermatologique aqueuse comprenant une mérocyanine et un filtre UV hydrosoluble |
| FR3149780A1 (fr) | 2023-06-16 | 2024-12-20 | L'oreal | Composition comprenant au moins 1 % en poids d’acide ascorbique, un filtre UV organique hydrosoluble et des filtres UV addditionnels |
| FR3149778A1 (fr) | 2023-06-16 | 2024-12-20 | L'oreal | Composition comprenant au moins 1 % en poids d’acide ascorbique et un polymère lipophile convenablement sélectionné |
| WO2025024904A1 (en) | 2023-07-28 | 2025-02-06 | L'oreal | Cosmetic composition, use of the cosmetic composition and process for manufacturing the cosmetic composition |
| FR3156034A1 (fr) | 2023-12-01 | 2025-06-06 | L'oreal | Composition comprenant un filtre UV organique lipophile, un tensioactif géminé, un polymère semi-cristallin contenant au moins une chaine d’alkyl acrylate et un polyol |
| FR3156035A1 (fr) | 2023-12-01 | 2025-06-06 | L'oreal | Composition comprenant un filtre UV organique lipophile, un tensioactif géminé et un tensioactif anionique dérivé d’un acide aminé |
| FR3156037A1 (fr) | 2023-12-01 | 2025-06-06 | L'oreal | Composition comprenant un filtre UV organique lipophile, un tensioactif géminé et au moins 8 % en poids d’un mono-alcool en C1-C4 |
| WO2025114438A1 (en) | 2023-12-01 | 2025-06-05 | L'oreal | Composition comprising a lipophilic organic uv-screening agent, a gemini surfactant and at least 8% by weight of a c1-c4 monoalcohol |
| FR3157116A1 (fr) | 2023-12-20 | 2025-06-27 | L'oreal | Composition cosmétique sous la forme d’une émulsion huile-dans-eau comprenant de l’acide ascorbique, au moins un filtre solaire, et gélifiée par des polymères naturels |
| WO2025141605A1 (en) | 2023-12-27 | 2025-07-03 | L'oreal | A formulation of punica granatum extract with enhanced stability and applications thereof |
| FR3157800A1 (fr) | 2023-12-28 | 2025-07-04 | L'oreal | Composition cosmétique sous la forme d’une émulsion huile-dans-eau comprenant un filtre UV organique lipophile et son utilisation en cosmétique |
| WO2025156021A1 (en) | 2024-01-24 | 2025-07-31 | L'oreal | Tinted sunscreen compositions, process for manufacturing a tinted sunscreen composition, and use of a tinted sunscreen composition |
| FR3161116A1 (fr) | 2024-04-11 | 2025-10-17 | L'oreal | Composition comprenant un filtre UV organique, un polymère gélifiant hydrophile spécifique et un ester d’acide gras et de sucre |
| FR3161108A1 (fr) | 2024-04-11 | 2025-10-17 | L'oreal | Composition comprenant le Drometrizole Trisiloxane, un filtre organique hydrophile, avec un ratio massique filtres organiques hydrophiles / filtres organiques lipophiles supérieur à 0,3, sans alcool |
| FR3162627A1 (fr) | 2024-06-04 | 2025-12-05 | L'oreal | Composition cosmétique comprenant des filtres UVA organiques hydrophiles ou hydrodispersibles |
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- 2004-03-19 ES ES04721908T patent/ES2435512T3/es not_active Expired - Lifetime
- 2004-03-19 AU AU2004224086A patent/AU2004224086B2/en not_active Expired
- 2004-03-19 US US10/804,676 patent/US7311897B2/en active Active
- 2004-03-19 KR KR1020057016980A patent/KR101187002B1/ko not_active Expired - Lifetime
- 2004-03-19 EP EP04721908.4A patent/EP1606270B1/en not_active Expired - Lifetime
- 2004-03-19 MX MXPA05010167 patent/MX267068B/es active IP Right Grant
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| EP1606270A2 (en) | 2005-12-21 |
| KR101187002B1 (ko) | 2012-09-28 |
| JP4764817B2 (ja) | 2011-09-07 |
| KR20050114231A (ko) | 2005-12-05 |
| JP2006523197A (ja) | 2006-10-12 |
| EP1606270B1 (en) | 2013-08-14 |
| AU2004224086A1 (en) | 2004-10-07 |
| WO2004085412A3 (en) | 2005-02-10 |
| US20040191191A1 (en) | 2004-09-30 |
| BRPI0408994A (pt) | 2006-03-28 |
| TWI331997B (en) | 2010-10-21 |
| US7311897B2 (en) | 2007-12-25 |
| WO2004085412A2 (en) | 2004-10-07 |
| TW200503771A (en) | 2005-02-01 |
| BRPI0408994B1 (pt) | 2015-07-14 |
| MX267068B (es) | 2009-05-29 |
| ES2435512T3 (es) | 2013-12-20 |
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