ES2284634T3 - Fotoestabilizacion de derivados de dibenzoilmetano. - Google Patents
Fotoestabilizacion de derivados de dibenzoilmetano. Download PDFInfo
- Publication number
- ES2284634T3 ES2284634T3 ES01923464T ES01923464T ES2284634T3 ES 2284634 T3 ES2284634 T3 ES 2284634T3 ES 01923464 T ES01923464 T ES 01923464T ES 01923464 T ES01923464 T ES 01923464T ES 2284634 T3 ES2284634 T3 ES 2284634T3
- Authority
- ES
- Spain
- Prior art keywords
- dibenzoylmethane
- bis
- phenyl
- triazine
- hydroxy
- Prior art date
- 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
Links
- 230000000176 photostabilization Effects 0.000 title description 2
- 239000000203 mixture Substances 0.000 claims abstract description 63
- NZZIMKJIVMHWJC-UHFFFAOYSA-N dibenzoylmethane Chemical class C=1C=CC=CC=1C(=O)CC(=O)C1=CC=CC=C1 NZZIMKJIVMHWJC-UHFFFAOYSA-N 0.000 claims abstract description 41
- 239000002537 cosmetic Substances 0.000 claims abstract description 27
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims abstract description 21
- 230000005855 radiation Effects 0.000 claims abstract description 20
- -1 2-ethylhexyloxy Chemical group 0.000 claims description 41
- 238000009472 formulation Methods 0.000 claims description 23
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- 235000013985 cinnamic acid Nutrition 0.000 claims description 10
- WBYWAXJHAXSJNI-UHFFFAOYSA-N methyl p-hydroxycinnamate Natural products OC(=O)C=CC1=CC=CC=C1 WBYWAXJHAXSJNI-UHFFFAOYSA-N 0.000 claims description 10
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- DLAHAXOYRFRPFQ-UHFFFAOYSA-N dodecyl benzoate Chemical compound CCCCCCCCCCCCOC(=O)C1=CC=CC=C1 DLAHAXOYRFRPFQ-UHFFFAOYSA-N 0.000 description 5
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- 125000000217 alkyl group Chemical group 0.000 description 4
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- 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 3
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- NWGKJDSIEKMTRX-BFWOXRRGSA-N [(2r)-2-[(3r,4s)-3,4-dihydroxyoxolan-2-yl]-2-hydroxyethyl] (z)-octadec-9-enoate Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OC[C@@H](O)C1OC[C@H](O)[C@H]1O NWGKJDSIEKMTRX-BFWOXRRGSA-N 0.000 description 3
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- HEAHZSUCFKFERC-LRVMPXQBSA-N [(2e)-2-[[4-[(z)-[7,7-dimethyl-3-oxo-4-(sulfomethyl)-2-bicyclo[2.2.1]heptanylidene]methyl]phenyl]methylidene]-7,7-dimethyl-3-oxo-4-bicyclo[2.2.1]heptanyl]methanesulfonic acid Chemical compound CC1(C)C2CCC1(CS(O)(=O)=O)C(=O)\C2=C/C(C=C1)=CC=C1\C=C/1C(=O)C2(CS(O)(=O)=O)CCC\1C2(C)C HEAHZSUCFKFERC-LRVMPXQBSA-N 0.000 description 1
- 239000006096 absorbing agent Substances 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 230000001476 alcoholic effect Effects 0.000 description 1
- 125000003545 alkoxy group Chemical group 0.000 description 1
- 235000011399 aloe vera Nutrition 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 229940064734 aminobenzoate Drugs 0.000 description 1
- 229960004050 aminobenzoic acid Drugs 0.000 description 1
- 229940058303 antinematodal benzimidazole derivative Drugs 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 229960005193 avobenzone Drugs 0.000 description 1
- 235000013871 bee wax Nutrition 0.000 description 1
- 239000012166 beeswax Substances 0.000 description 1
- 125000003785 benzimidazolyl group Chemical class N1=C(NC2=C1C=CC=C2)* 0.000 description 1
- 150000001558 benzoic acid derivatives Chemical class 0.000 description 1
- 239000012965 benzophenone Substances 0.000 description 1
- 235000019445 benzyl alcohol Nutrition 0.000 description 1
- 230000005540 biological transmission Effects 0.000 description 1
- 235000020958 biotin Nutrition 0.000 description 1
- 229960002685 biotin Drugs 0.000 description 1
- 239000011616 biotin Substances 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000000084 colloidal system Substances 0.000 description 1
- 230000000295 complement effect Effects 0.000 description 1
- 239000013068 control sample Substances 0.000 description 1
- 229920006037 cross link polymer Polymers 0.000 description 1
- 238000006352 cycloaddition reaction Methods 0.000 description 1
- GVJHHUAWPYXKBD-UHFFFAOYSA-N d-alpha-tocopherol Natural products OC1=C(C)C(C)=C2OC(CCCC(C)CCCC(C)CCCC(C)C)(C)CCC2=C1C GVJHHUAWPYXKBD-UHFFFAOYSA-N 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 230000018109 developmental process Effects 0.000 description 1
- 229960003949 dexpanthenol Drugs 0.000 description 1
- 150000005690 diesters Chemical class 0.000 description 1
- 229960003747 ecamsule Drugs 0.000 description 1
- HEOCBCNFKCOKBX-SDNWHVSQSA-N enzacamene Chemical compound C1=CC(C)=CC=C1\C=C/1C(=O)C2(C)CCC\1C2(C)C HEOCBCNFKCOKBX-SDNWHVSQSA-N 0.000 description 1
- 229960004756 ethanol Drugs 0.000 description 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 150000002191 fatty alcohols Chemical class 0.000 description 1
- 230000009931 harmful effect Effects 0.000 description 1
- ZUVCYFMOHFTGDM-UHFFFAOYSA-N hexadecyl dihydrogen phosphate Chemical compound CCCCCCCCCCCCCCCCOP(O)(O)=O ZUVCYFMOHFTGDM-UHFFFAOYSA-N 0.000 description 1
- 238000000265 homogenisation Methods 0.000 description 1
- 229920001519 homopolymer Polymers 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 238000011534 incubation Methods 0.000 description 1
- 238000009434 installation Methods 0.000 description 1
- 230000001678 irradiating effect Effects 0.000 description 1
- 229940001447 lactate Drugs 0.000 description 1
- 239000000865 liniment Substances 0.000 description 1
- 239000002502 liposome Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 238000004811 liquid chromatography Methods 0.000 description 1
- 229940057995 liquid paraffin Drugs 0.000 description 1
- 239000011976 maleic acid Substances 0.000 description 1
- 239000004530 micro-emulsion Substances 0.000 description 1
- 235000013336 milk Nutrition 0.000 description 1
- 239000008267 milk Substances 0.000 description 1
- 210000004080 milk Anatomy 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 235000010446 mineral oil Nutrition 0.000 description 1
- 238000005065 mining Methods 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 230000001333 moisturizer Effects 0.000 description 1
- GOQYKNQRPGWPLP-UHFFFAOYSA-N n-heptadecyl alcohol Natural products CCCCCCCCCCCCCCCCCO GOQYKNQRPGWPLP-UHFFFAOYSA-N 0.000 description 1
- VXBBHHIEFUJAEX-UHFFFAOYSA-N n-pentan-3-ylbenzamide Chemical compound CCC(CC)NC(=O)C1=CC=CC=C1 VXBBHHIEFUJAEX-UHFFFAOYSA-N 0.000 description 1
- NGCURIJPLVFJJH-UHFFFAOYSA-N n-phenyltriazin-4-amine Chemical class C=1C=NN=NC=1NC1=CC=CC=C1 NGCURIJPLVFJJH-UHFFFAOYSA-N 0.000 description 1
- 239000007908 nanoemulsion Substances 0.000 description 1
- 239000006070 nanosuspension Substances 0.000 description 1
- 239000006199 nebulizer Substances 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- FMJSMJQBSVNSBF-UHFFFAOYSA-N octocrylene Chemical group C=1C=CC=CC=1C(=C(C#N)C(=O)OCC(CC)CCCC)C1=CC=CC=C1 FMJSMJQBSVNSBF-UHFFFAOYSA-N 0.000 description 1
- 229960000601 octocrylene Drugs 0.000 description 1
- INGMGRULDUBWPK-UHFFFAOYSA-N octyl 4-amino-2,3-dimethylbenzoate Chemical compound CCCCCCCCOC(=O)C1=CC=C(N)C(C)=C1C INGMGRULDUBWPK-UHFFFAOYSA-N 0.000 description 1
- 229940056211 paraffin Drugs 0.000 description 1
- 239000006072 paste Substances 0.000 description 1
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 1
- 239000002304 perfume Substances 0.000 description 1
- 230000002085 persistent effect Effects 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 239000000256 polyoxyethylene sorbitan monolaurate Substances 0.000 description 1
- 235000010486 polyoxyethylene sorbitan monolaurate Nutrition 0.000 description 1
- 230000002028 premature Effects 0.000 description 1
- 239000011814 protection agent Substances 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 150000003902 salicylic acid esters Chemical class 0.000 description 1
- 239000000523 sample Substances 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 235000021003 saturated fats Nutrition 0.000 description 1
- 150000003377 silicon compounds Chemical class 0.000 description 1
- 230000009759 skin aging Effects 0.000 description 1
- 201000000849 skin cancer Diseases 0.000 description 1
- 230000037380 skin damage Effects 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 230000007928 solubilization Effects 0.000 description 1
- 238000005063 solubilization Methods 0.000 description 1
- 239000004334 sorbic acid Substances 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
- 238000011105 stabilization Methods 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 239000005720 sucrose Substances 0.000 description 1
- 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
- 229960000368 sulisobenzone Drugs 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 239000004408 titanium dioxide Substances 0.000 description 1
- 229960001295 tocopherol Drugs 0.000 description 1
- 235000010384 tocopherol Nutrition 0.000 description 1
- 229930003799 tocopherol Natural products 0.000 description 1
- 239000011732 tocopherol Substances 0.000 description 1
- 229940042585 tocopherol acetate Drugs 0.000 description 1
- 150000003626 triacylglycerols Chemical class 0.000 description 1
- 150000005691 triesters Chemical class 0.000 description 1
- 229960004418 trolamine Drugs 0.000 description 1
- 229940088594 vitamin Drugs 0.000 description 1
- 239000011782 vitamin Substances 0.000 description 1
- 229930003231 vitamin Natural products 0.000 description 1
- 235000013343 vitamin Nutrition 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
- GVJHHUAWPYXKBD-IEOSBIPESA-N α-tocopherol Chemical compound OC1=C(C)C(C)=C2O[C@@](CCC[C@H](C)CCC[C@H](C)CCCC(C)C)(C)CCC2=C1C GVJHHUAWPYXKBD-IEOSBIPESA-N 0.000 description 1
Classifications
-
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/33—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
- A61K8/35—Ketones, e.g. benzophenone
-
- 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
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K2800/00—Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
- A61K2800/40—Chemical, physico-chemical or functional or structural properties of particular ingredients
- A61K2800/52—Stabilizers
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Epidemiology (AREA)
- Birds (AREA)
- Emergency Medicine (AREA)
- Dermatology (AREA)
- Cosmetics (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Anti-Oxidant Or Stabilizer Compositions (AREA)
- Steroid Compounds (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CH9332000 | 2000-05-12 | ||
| CH93300/00 | 2000-05-12 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ES2284634T3 true ES2284634T3 (es) | 2007-11-16 |
Family
ID=4548916
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES01923464T Expired - Lifetime ES2284634T3 (es) | 2000-05-12 | 2001-05-03 | Fotoestabilizacion de derivados de dibenzoilmetano. |
Country Status (8)
| Country | Link |
|---|---|
| US (1) | US6803063B2 (enExample) |
| EP (1) | EP1280505B1 (enExample) |
| JP (2) | JP5528651B2 (enExample) |
| AT (1) | ATE361123T1 (enExample) |
| AU (1) | AU2001250237A1 (enExample) |
| DE (1) | DE50112444D1 (enExample) |
| ES (1) | ES2284634T3 (enExample) |
| WO (1) | WO2001085123A1 (enExample) |
Families Citing this family (25)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2833169B1 (fr) * | 2001-12-07 | 2004-07-16 | Oreal | Composition filtrante contenant un derive de 1,3,5-triazine, un derive du dibenzoylmethane, et un derive de 2-hydroxybenzophenone aminosubstitue |
| FR2833168B1 (fr) | 2001-12-07 | 2004-08-27 | Oreal | Composition filtrante contenant un filtre du type derive du dibenzoylmethane et un derive de 2-hydroxybenzophenone aminosubstitue |
| DE10210337A1 (de) * | 2002-03-08 | 2003-09-25 | Beiersdorf Ag | Lippenpflegeprodukte mit UV-Schutz |
| DE10229997A1 (de) * | 2002-07-03 | 2004-01-15 | Beiersdorf Ag | Kosmetische oder dermatologische Zubereitung zum Schutz fotolabiler Wirkstoffe |
| FR2847811B1 (fr) * | 2002-11-29 | 2005-01-07 | Oreal | Composition filtrante contenant au moins un derive du dibenzoylmethane et au moins un derive de 3-(2-azacycloalkylidene)-1,3-dihydro-indol-2-one;procede de photostabilisation |
| GB0318160D0 (en) * | 2003-08-02 | 2003-09-03 | Ssl Int Plc | Parasiticidal composition |
| DE102004020060B3 (de) * | 2004-04-20 | 2005-06-02 | Coty B.V. | Kosmetisches Verfahren zur Behandlung der Haut mit Sonnenprodukten und Sonnenprodukt-Kombination |
| US7368105B2 (en) | 2004-07-02 | 2008-05-06 | L'oreal | Photostabilization of dibenzoylmethane UV-screening agents with arylalkyl benzoate/bis-resorcinyl triazine compounds and photoprotective compositions comprised thereof |
| FR2872414B1 (fr) | 2004-07-02 | 2006-09-22 | Oreal | Procede de photostabilisation d'un derive de dibenzoylmethane par un derive arylalkyl benzoate et un compose bis-resorcinyl triazine et compositions cosmetiques photoprotectrices |
| US7357919B2 (en) | 2004-10-19 | 2008-04-15 | L'oreal | Photostable photoprotective compositions comprising dibenzoylmethane and arylalkyl benzoate compounds and a compound that accepts the excited triplet level energy of said dibenzoylmethane(s) |
| US7431917B2 (en) * | 2004-10-19 | 2008-10-07 | L'oreal | Photostable photoprotective compositions comprising dibenzoylmethane and bis-resorcinyl triazine compounds and a compound that accepts the excited triplet level energy of said dibenzoylmethane(s) |
| FR2876579B1 (fr) * | 2004-10-19 | 2007-04-13 | Oreal | Composition antisolaire a base d'un derive de dibenzoylmetha ne et d'un agent photostabilisant particulier;procede de pho tostabilisation |
| FR2886144B1 (fr) * | 2005-05-27 | 2007-06-29 | Oreal | Procede de photostabilisation d'un derive de dibenzoylmethane par un derive sulfone de merocyanine ; compositions cosmetiques photoprotectrices contenant cette associaton. |
| FR2908988B1 (fr) * | 2006-11-28 | 2009-01-23 | Oreal | Photostabilisation d'un dibenzoylmethane par une s-triazine siliciee et substituee par deux groupes aminobenzaotes ou aminobenzamides et une bis-resorcinyltriazine; compositions photoprotectrices contenant cette association ternaire |
| KR102127963B1 (ko) * | 2007-08-30 | 2020-06-29 | 바스프 에스이 | 미용 조성물의 안정화 |
| FR2949326B1 (fr) * | 2009-08-28 | 2012-02-17 | Oreal | Composition contenant un derive de dibenzoylmethane, une 2-hydroxybenzophenone lipophile et une s-triazine siliciee ; procede de photostabilisation |
| ES2608456T3 (es) | 2009-08-28 | 2017-04-11 | L'oréal | Composición que contiene al menos un filtro de tipo 2-hidroxibenzofenona lipófila y una s-triazina siliciada sustituida por al menos dos grupos alquilaminobenzoatos |
| DE102010044682A1 (de) | 2010-09-08 | 2012-03-08 | Beiersdorf Ag | Emulsion mit UV-Schutz |
| DE102010044681A1 (de) | 2010-09-08 | 2012-03-08 | Beiersdorf Ag | Stabilisierte Emulsion |
| FR2978041B1 (fr) * | 2011-07-21 | 2014-01-10 | Lvmh Rech | Solution parfumante stabilisee vis-a-vis des rayons ultraviolets |
| WO2013114004A1 (fr) | 2012-01-31 | 2013-08-08 | Pierre Fabre Dermo-Cosmetique | Composition et association de filtres solaires photostabilisatrices de bmdbm |
| CA2880772C (en) | 2012-08-06 | 2020-11-17 | Unilever Plc | A photostable sunscreen composition |
| DE102013204097A1 (de) * | 2013-03-11 | 2014-10-30 | Beiersdorf Ag | Wirkstoffkombinationen aus Alkylamidothiazolen und einer oder mehreren kosmetisch oder dermatologisch unbedenklichen UV-Filtersubstanzen |
| EP3817731B1 (en) * | 2018-07-05 | 2025-09-03 | Celista Pharmaceuticals Llc | Testosterone and estradiol transdermal spray |
| WO2020217499A1 (ja) | 2019-04-26 | 2020-10-29 | 大塚製薬株式会社 | アデノシンリン酸を含有するｏ／ｗ型低粘度乳化組成物 |
Family Cites Families (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| IT1286504B1 (it) * | 1996-11-26 | 1998-07-15 | 3V Sigma Spa | Composizioni cosmetiche antisolari comprendenti derivati del dibenzoilmetano del benzofenone e della triazina |
| FR2763851B1 (fr) * | 1997-05-28 | 1999-07-09 | Oreal | Compositions comprenant un derive de dibenzoylmethane et un polymere polyamine |
| DE19756921A1 (de) * | 1997-12-19 | 1999-06-24 | Beiersdorf Ag | Verwendung von synthetischem Bienenwachs zur Verstärkung der UV-A-Schutzleistung kosmetischer oder dermatologischer Formulierungen |
| DE19833634A1 (de) * | 1998-07-25 | 2000-02-03 | Beiersdorf Ag | Kosmetische oder dermatologische W/O-Emulsionen, welche nichtionische Tenside enthalten und sich durch einen Gehalt an Siliconemulatoren auszeichnen |
| DE19846772A1 (de) | 1998-10-10 | 2000-04-13 | Beiersdorf Ag | Kosmetische und dermatoligische Hydrodispersionen mit einem Gehalt an Triglyceridwachsen |
| DE19910477A1 (de) * | 1999-03-10 | 2000-09-14 | Beiersdorf Ag | Verwendung von Octocrylen zur Solubilisierung von 2,4-Bis-{[4-(2-Ethyl-hexyloxy-2-hydroxy]-phenyl}-6-(4-methoxyphenyl)-1,3,5-triazin in kosmetischen oder dermatologischen Lichtschutzmitteln |
| NO20002309L (no) * | 1999-05-12 | 2000-11-13 | Hoffmann La Roche | Fotostabile kosmetiske lysavskjermende sammensetninger |
-
2001
- 2001-05-03 US US10/275,870 patent/US6803063B2/en not_active Expired - Lifetime
- 2001-05-03 AU AU2001250237A patent/AU2001250237A1/en not_active Abandoned
- 2001-05-03 AT AT01923464T patent/ATE361123T1/de not_active IP Right Cessation
- 2001-05-03 EP EP01923464A patent/EP1280505B1/de not_active Expired - Lifetime
- 2001-05-03 DE DE50112444T patent/DE50112444D1/de not_active Expired - Lifetime
- 2001-05-03 ES ES01923464T patent/ES2284634T3/es not_active Expired - Lifetime
- 2001-05-03 JP JP2001581778A patent/JP5528651B2/ja not_active Expired - Lifetime
- 2001-05-03 WO PCT/CH2001/000275 patent/WO2001085123A1/de not_active Ceased
-
2012
- 2012-06-06 JP JP2012129059A patent/JP5554373B2/ja not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| EP1280505A1 (de) | 2003-02-05 |
| JP5554373B2 (ja) | 2014-07-23 |
| DE50112444D1 (de) | 2007-06-14 |
| US20030185770A1 (en) | 2003-10-02 |
| WO2001085123A1 (de) | 2001-11-15 |
| JP2012188445A (ja) | 2012-10-04 |
| ATE361123T1 (de) | 2007-05-15 |
| JP2003532665A (ja) | 2003-11-05 |
| AU2001250237A1 (en) | 2001-11-20 |
| US6803063B2 (en) | 2004-10-12 |
| EP1280505B1 (de) | 2007-05-02 |
| JP5528651B2 (ja) | 2014-06-25 |
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