ES2333197T3 - Mezclas de micropigmentos. - Google Patents
Mezclas de micropigmentos. Download PDFInfo
- Publication number
- ES2333197T3 ES2333197T3 ES00949173T ES00949173T ES2333197T3 ES 2333197 T3 ES2333197 T3 ES 2333197T3 ES 00949173 T ES00949173 T ES 00949173T ES 00949173 T ES00949173 T ES 00949173T ES 2333197 T3 ES2333197 T3 ES 2333197T3
- Authority
- ES
- Spain
- Prior art keywords
- mixtures
- bis
- methylene
- benzotriazolyltetramethylbutylphenol
- formula
- 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
- 239000000203 mixture Substances 0.000 title claims abstract description 74
- 239000004904 UV filter Substances 0.000 claims abstract description 38
- 239000002537 cosmetic Substances 0.000 claims abstract description 15
- 241001465754 Metazoa Species 0.000 claims abstract description 4
- 150000001875 compounds Chemical class 0.000 claims description 38
- FQUNFJULCYSSOP-UHFFFAOYSA-N bisoctrizole Chemical compound N1=C2C=CC=CC2=NN1C1=CC(C(C)(C)CC(C)(C)C)=CC(CC=2C(=C(C=C(C=2)C(C)(C)CC(C)(C)C)N2N=C3C=CC=CC3=N2)O)=C1O FQUNFJULCYSSOP-UHFFFAOYSA-N 0.000 claims description 32
- JGUMTYWKIBJSTN-UHFFFAOYSA-N 2-ethylhexyl 4-[[4,6-bis[4-(2-ethylhexoxycarbonyl)anilino]-1,3,5-triazin-2-yl]amino]benzoate Chemical compound C1=CC(C(=O)OCC(CC)CCCC)=CC=C1NC1=NC(NC=2C=CC(=CC=2)C(=O)OCC(CC)CCCC)=NC(NC=2C=CC(=CC=2)C(=O)OCC(CC)CCCC)=N1 JGUMTYWKIBJSTN-UHFFFAOYSA-N 0.000 claims description 21
- 230000004224 protection Effects 0.000 claims description 15
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- 239000012530 fluid Substances 0.000 claims description 4
- 230000009931 harmful effect Effects 0.000 claims description 4
- 125000000129 anionic group Chemical group 0.000 claims description 3
- 239000003814 drug Substances 0.000 claims description 3
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- 230000003078 antioxidant effect Effects 0.000 claims description 2
- 239000012860 organic pigment Substances 0.000 claims description 2
- 239000001023 inorganic pigment Substances 0.000 claims 2
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- ALYNCZNDIQEVRV-UHFFFAOYSA-N 4-aminobenzoic acid Chemical class NC1=CC=C(C(O)=O)C=C1 ALYNCZNDIQEVRV-UHFFFAOYSA-N 0.000 description 8
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- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 6
- 239000006096 absorbing agent Substances 0.000 description 6
- 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 6
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- DSSYKIVIOFKYAU-XCBNKYQSSA-N (R)-camphor Chemical class C1C[C@@]2(C)C(=O)C[C@@H]1C2(C)C DSSYKIVIOFKYAU-XCBNKYQSSA-N 0.000 description 4
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- 239000003213 antiperspirant Substances 0.000 description 4
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 4
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- GFQYVLUOOAAOGM-UHFFFAOYSA-N zirconium(iv) silicate Chemical compound [Zr+4].[O-][Si]([O-])([O-])[O-] GFQYVLUOOAAOGM-UHFFFAOYSA-N 0.000 description 4
- VKTKSVRJLNRCQA-UHFFFAOYSA-N 2-[1,1-bis(2H-benzotriazol-4-yl)butyl]-3,4,5,6-tetramethylphenol Chemical compound N1N=NC2=C1C=CC=C2C(CCC)(C1=C(C(=C(C(=C1C)C)C)C)O)C1=CC=CC=2NN=NC=21 VKTKSVRJLNRCQA-UHFFFAOYSA-N 0.000 description 3
- GGHBKCSNURXPNB-UHFFFAOYSA-N 2-n,4-n,6-n-triphenyl-1,3,5-triazine-2,4,6-triamine Chemical class N=1C(NC=2C=CC=CC=2)=NC(NC=2C=CC=CC=2)=NC=1NC1=CC=CC=C1 GGHBKCSNURXPNB-UHFFFAOYSA-N 0.000 description 3
- 241000723346 Cinnamomum camphora Species 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 3
- 125000000217 alkyl group Chemical group 0.000 description 3
- 229960004050 aminobenzoic acid Drugs 0.000 description 3
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- 239000011787 zinc oxide Substances 0.000 description 3
- MIOPJNTWMNEORI-GMSGAONNSA-N (S)-camphorsulfonic acid Chemical compound C1C[C@@]2(CS(O)(=O)=O)C(=O)C[C@@H]1C2(C)C MIOPJNTWMNEORI-GMSGAONNSA-N 0.000 description 2
- IANQTJSKSUMEQM-UHFFFAOYSA-N 1-benzofuran Chemical compound C1=CC=C2OC=CC2=C1 IANQTJSKSUMEQM-UHFFFAOYSA-N 0.000 description 2
- XDOFQFKRPWOURC-UHFFFAOYSA-N 16-methylheptadecanoic acid Chemical compound CC(C)CCCCCCCCCCCCCCC(O)=O XDOFQFKRPWOURC-UHFFFAOYSA-N 0.000 description 2
- OSCJHTSDLYVCQC-UHFFFAOYSA-N 2-ethylhexyl 4-[[4-[4-(tert-butylcarbamoyl)anilino]-6-[4-(2-ethylhexoxycarbonyl)anilino]-1,3,5-triazin-2-yl]amino]benzoate Chemical compound C1=CC(C(=O)OCC(CC)CCCC)=CC=C1NC1=NC(NC=2C=CC(=CC=2)C(=O)NC(C)(C)C)=NC(NC=2C=CC(=CC=2)C(=O)OCC(CC)CCCC)=N1 OSCJHTSDLYVCQC-UHFFFAOYSA-N 0.000 description 2
- WMJBVALTYVXGHW-UHFFFAOYSA-N 3,3-diphenylprop-2-enoic acid Chemical class C=1C=CC=CC=1C(=CC(=O)O)C1=CC=CC=C1 WMJBVALTYVXGHW-UHFFFAOYSA-N 0.000 description 2
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
- LZZYPRNAOMGNLH-UHFFFAOYSA-M Cetrimonium bromide Chemical compound [Br-].CCCCCCCCCCCCCCCC[N+](C)(C)C LZZYPRNAOMGNLH-UHFFFAOYSA-M 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- GLZPCOQZEFWAFX-UHFFFAOYSA-N Geraniol Chemical compound CC(C)=CCCC(C)=CCO GLZPCOQZEFWAFX-UHFFFAOYSA-N 0.000 description 2
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 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
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
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- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 2
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- 239000000443 aerosol Substances 0.000 description 2
- 150000001565 benzotriazoles Chemical class 0.000 description 2
- 238000005266 casting Methods 0.000 description 2
- 125000002091 cationic group Chemical group 0.000 description 2
- 150000001793 charged compounds Chemical class 0.000 description 2
- 230000035614 depigmentation Effects 0.000 description 2
- NZZIMKJIVMHWJC-UHFFFAOYSA-N dibenzoylmethane Chemical class C=1C=CC=CC=1C(=O)CC(=O)C1=CC=CC=C1 NZZIMKJIVMHWJC-UHFFFAOYSA-N 0.000 description 2
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- WIGCFUFOHFEKBI-UHFFFAOYSA-N gamma-tocopherol Natural products CC(C)CCCC(C)CCCC(C)CCCC1CCC2C(C)C(O)C(C)C(C)C2O1 WIGCFUFOHFEKBI-UHFFFAOYSA-N 0.000 description 2
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- 238000002844 melting Methods 0.000 description 2
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- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 2
- 239000010445 mica Substances 0.000 description 2
- 229910052618 mica group Inorganic materials 0.000 description 2
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Classifications
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- 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
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- 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
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- 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
- A61K8/4906—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds with one nitrogen as the only hetero atom
- A61K8/4913—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds with one nitrogen as the only hetero atom having five membered rings, e.g. pyrrolidone carboxylic acid
- A61K8/492—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds with one nitrogen as the only hetero atom having five membered rings, e.g. pyrrolidone carboxylic acid having condensed rings, e.g. indol
-
- 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
- A61K8/4946—Imidazoles or their condensed derivatives, e.g. benzimidazoles
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- 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
- A61K8/496—Triazoles or their condensed derivatives, e.g. benzotriazoles
-
- 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
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
- A61P17/16—Emollients or protectives, e.g. against radiation
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- 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
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- 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
- A61K2800/41—Particular ingredients further characterized by their size
- A61K2800/412—Microsized, i.e. having sizes between 0.1 and 100 microns
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)
- Birds (AREA)
- Epidemiology (AREA)
- Dermatology (AREA)
- Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Toxicology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Organic Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Cosmetics (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Tea And Coffee (AREA)
- Saccharide Compounds (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP99810543 | 1999-06-18 | ||
| EP99810543 | 1999-06-18 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ES2333197T3 true ES2333197T3 (es) | 2010-02-18 |
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Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES00949173T Expired - Lifetime ES2333197T3 (es) | 1999-06-18 | 2000-06-08 | Mezclas de micropigmentos. |
Country Status (13)
| Country | Link |
|---|---|
| US (1) | US6746666B1 (enExample) |
| EP (1) | EP1187598B1 (enExample) |
| JP (1) | JP4744754B2 (enExample) |
| KR (1) | KR100759240B1 (enExample) |
| CN (1) | CN1221244C (enExample) |
| AT (1) | ATE446124T1 (enExample) |
| AU (1) | AU778175B2 (enExample) |
| BR (1) | BR0011766A (enExample) |
| DE (1) | DE50015768D1 (enExample) |
| ES (1) | ES2333197T3 (enExample) |
| IL (1) | IL146778A0 (enExample) |
| MX (1) | MX231178B (enExample) |
| WO (1) | WO2000078277A1 (enExample) |
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| Publication number | Priority date | Publication date | Assignee | Title |
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| AU774383B2 (en) * | 1999-07-12 | 2004-06-24 | Ciba Specialty Chemicals Holding Inc. | Use of mixtures of micropigments for preventing tanning and for lightening skin and hair |
| AU2002210469A1 (en) * | 2000-08-29 | 2002-03-13 | Ciba Specialty Chemicals Holding Inc. | Sunscreen compositions containing triazine derivatives and triazole derivatives |
| FR2816842B1 (fr) * | 2000-11-17 | 2005-03-11 | Oreal | Filtres uv organiques insolubles et leur utilisation en cosmetique |
| FR2818128B1 (fr) * | 2000-12-18 | 2004-04-02 | Oreal | Compositions cosmetiques antisolaires a base d'un melange synergetique de filtres et utilisations |
| DE10100721A1 (de) * | 2001-01-10 | 2002-07-11 | Beiersdorf Ag | Wässrige kosmetische und dermatologische Zubereitungen mit einem Gehalt an wasserlöslichen UV-Filtersubstanzen |
| FR2819180B1 (fr) * | 2001-01-11 | 2003-02-21 | Oreal | Composition photoprotectrices a base de polymeres amphiphiles d'au moins un monomere a insaturation ethylique a groupement sulfonique et comportant une partie hydrophobe |
| JP4993421B2 (ja) * | 2001-06-07 | 2012-08-08 | 株式会社Ａｄｅｋａ | 合成樹脂組成物 |
| AU2003205656B2 (en) * | 2002-01-31 | 2007-09-06 | Ciba Specialty Chemicals Holding Inc. | Micropigment mixtures |
| BRPI0308369B1 (pt) * | 2002-03-12 | 2015-05-26 | Ciba Sc Holding Ag | Composição absorvedora de uv compreendendo um composto hidroxifeniltriazina e processo para a preparação do referido composto |
| EP1407757A1 (en) * | 2002-10-09 | 2004-04-14 | Ciba SC Holding AG | Preparation of micronised UV absorbers |
| US7534421B2 (en) | 2003-03-03 | 2009-05-19 | L'oreal | s-Triazine compounds bearing at least one para-aminobenzalmalonic salt substituent and photoprotective cosmetic compositions comprised thereof |
| CN101336870B (zh) * | 2003-03-24 | 2013-03-27 | 西巴特殊化学制品控股公司 | 均三嗪衍生物 |
| KR101187002B1 (ko) * | 2003-03-24 | 2012-09-28 | 시바 홀딩 인코포레이티드 | 대칭 트리아진 유도체 |
| US20050012594A1 (en) * | 2003-07-17 | 2005-01-20 | Youngtack Shim | Key assemblies and methods |
| BRPI0512183B8 (pt) | 2004-07-20 | 2016-09-13 | Ciba Sc Holding Ag | uso de uma classe de substância micronizada insolúvel ou levemente solúvel, composição cosmética ou dermatológica, e uso da mesma |
| ATE536168T1 (de) | 2004-09-01 | 2011-12-15 | Basf Se | Mikropartikuläre, organische, uv-absorbierende zusammensetzung |
| US9089494B2 (en) * | 2004-09-14 | 2015-07-28 | Coty S.A. | Ultra-violet inhibition system |
| DE102004047285A1 (de) * | 2004-09-27 | 2006-04-20 | Beiersdorf Ag | Organische Mikropigmente enthaltende kosmetische Lichtschutzemulsion |
| DE102005051858A1 (de) † | 2005-10-25 | 2007-04-26 | Beiersdorf Ag | Kosmetische Zubereitung mit 1,2-Alkandiol und Triazinen |
| US20070224154A1 (en) * | 2006-03-21 | 2007-09-27 | Access Business Group International, Llc | Methods of reducing skin irritation |
| EP2076767A2 (en) * | 2006-10-26 | 2009-07-08 | Ciba Holding Inc. | Light absorbing layer for photo-chromic systems |
| JP5165978B2 (ja) * | 2007-09-20 | 2013-03-21 | 株式会社 資生堂 | 油中水型固形乳化化粧料 |
| EP3381445B1 (en) | 2007-11-15 | 2023-10-25 | Amgen Inc. | Aqueous formulation of antibody stablised by antioxidants for parenteral administration |
| KR101006343B1 (ko) * | 2008-07-31 | 2011-01-10 | 주식회사 코리아나화장품 | 이산화티탄의 유분산액을 함유하는 자외선 차단용 화장료조성물 |
| US20100040696A1 (en) * | 2008-08-12 | 2010-02-18 | Ilse Sente | Composite Particles Having An Antioxidant-Based Protective System, And Topical Compositions Comprising The Same |
| CN102292397B (zh) | 2009-01-19 | 2014-12-10 | 巴斯夫欧洲公司 | 有机黑色颜料及其制备 |
| KR101607880B1 (ko) | 2009-07-31 | 2016-04-01 | (주)아모레퍼시픽 | 자외선 차단용 화장료 조성물 |
| DE102009055281A1 (de) * | 2009-12-23 | 2011-06-30 | Henkel AG & Co. KGaA, 40589 | Emulsion für keratinhaltige Fasern, enthaltend mindestens ein anionisches verdickend wirkendes Polymer, mindestens ein nichtionisches haarfestigendes Polymer, mindestens ein Esteröl, mindestens ein Wachs und Wasser |
| KR101262037B1 (ko) * | 2010-10-04 | 2013-05-08 | 주식회사 선진화학 | 자외선 차단제의 표면처리층을 포함하는 복합분체의 신규한 제조방법 |
| WO2016175296A1 (ja) * | 2015-04-28 | 2016-11-03 | Tdk株式会社 | 樹脂組成物、樹脂シート、樹脂硬化物および樹脂基板 |
| MX375799B (es) * | 2016-10-11 | 2025-03-07 | Dsm Ip Assets Bv | Preparación de absorbedores de uv de tamaño nanométrico. |
| DE102019207780A1 (de) * | 2019-05-28 | 2020-12-03 | Beiersdorf Ag | Kosmetische O/W-Emulsion mit Skleroglucan und lipophilen UV-Filtersubstanzen |
| CN110974715B (zh) * | 2019-12-26 | 2023-08-01 | 常州纳欧新材料科技有限公司 | 一种apg改性mbbt复合材料及其水性浆料的制备方法 |
| DE102020204938A1 (de) * | 2020-04-20 | 2021-10-21 | Beiersdorf Aktiengesellschaft | Umweltfreundliches kosmetisches Sonnenschutzmittel |
Family Cites Families (17)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH03190814A (ja) * | 1989-12-21 | 1991-08-20 | Daikyo Rubber Seiko:Kk | 日焼け止め用化粧品 |
| JP3043903B2 (ja) * | 1992-06-29 | 2000-05-22 | ポーラ化成工業株式会社 | 粉体化粧料 |
| US5338539A (en) * | 1992-08-04 | 1994-08-16 | 3V Inc. | Benzofuran derivatives useful as sunscreens |
| US5445815A (en) * | 1993-11-22 | 1995-08-29 | Siegfried; Robert W. | Dry sunscreen composition |
| ATE204571T1 (de) * | 1993-11-23 | 2001-09-15 | Ciba Sc Holding Ag | O-hydroxyphenyl-s-triazine enthaltende stabilisierte polymere |
| GB9403451D0 (en) * | 1994-02-23 | 1994-04-13 | Ciba Geigy Ag | Sunscreen compositions |
| FR2720637B1 (fr) * | 1994-06-03 | 1996-07-26 | Oreal | Compositions cosmétiques photoprotectrices à base d'un mélange synergétique de filtres et utilisations. |
| US5601811A (en) | 1994-08-01 | 1997-02-11 | Croda, Inc. | Substantive water-soluble cationic UV-absorbing compounds |
| US5518713A (en) * | 1995-02-13 | 1996-05-21 | 3V Inc. | Benzoxazole derivatives, the use thereof as sunscreens and cosmetic compositions containing them |
| WO1997000851A1 (en) * | 1995-06-23 | 1997-01-09 | Zylepsis Limited | Chemical compounds and methods of production thereof |
| GB9515048D0 (en) * | 1995-07-22 | 1995-09-20 | Ciba Geigy Ag | Sunscreen compositions |
| DE59709127D1 (de) | 1996-07-08 | 2003-02-20 | Ciba Sc Holding Ag | Triazinderivate als UV-Filter in Sonnenschutzmitteln |
| EP0821939A1 (en) | 1996-07-31 | 1998-02-04 | 3V SIGMA S.p.A | Sun screening preparations comprising triazine derivatives |
| FR2763851B1 (fr) * | 1997-05-28 | 1999-07-09 | Oreal | Compositions comprenant un derive de dibenzoylmethane et un polymere polyamine |
| GB9715751D0 (en) * | 1997-07-26 | 1997-10-01 | Ciba Geigy Ag | Formulations |
| DE69941073D1 (de) * | 1998-03-02 | 2009-08-20 | Ciba Holding Inc | Verfahren zur Herstellung von 2,4-Diaryl-6-o-hydroxyphenyl-1,3,5-triazin Derivaten in Anwesenheit eines Protonensäure-Katalysators |
| AU774383B2 (en) * | 1999-07-12 | 2004-06-24 | Ciba Specialty Chemicals Holding Inc. | Use of mixtures of micropigments for preventing tanning and for lightening skin and hair |
-
2000
- 2000-06-08 BR BR0011766-8A patent/BR0011766A/pt not_active Application Discontinuation
- 2000-06-08 JP JP2001504342A patent/JP4744754B2/ja not_active Expired - Lifetime
- 2000-06-08 US US10/018,199 patent/US6746666B1/en not_active Expired - Lifetime
- 2000-06-08 KR KR1020017016207A patent/KR100759240B1/ko not_active Expired - Lifetime
- 2000-06-08 CN CNB008089337A patent/CN1221244C/zh not_active Expired - Lifetime
- 2000-06-08 DE DE50015768T patent/DE50015768D1/de not_active Expired - Lifetime
- 2000-06-08 AU AU62626/00A patent/AU778175B2/en not_active Expired
- 2000-06-08 MX MXPA01013101 patent/MX231178B/es active IP Right Grant
- 2000-06-08 EP EP00949173A patent/EP1187598B1/de not_active Expired - Lifetime
- 2000-06-08 WO PCT/EP2000/005314 patent/WO2000078277A1/de not_active Ceased
- 2000-06-08 AT AT00949173T patent/ATE446124T1/de not_active IP Right Cessation
- 2000-06-08 ES ES00949173T patent/ES2333197T3/es not_active Expired - Lifetime
- 2000-06-08 IL IL14677800A patent/IL146778A0/xx unknown
Also Published As
| Publication number | Publication date |
|---|---|
| JP2003502354A (ja) | 2003-01-21 |
| IL146778A0 (en) | 2002-07-25 |
| KR20020013584A (ko) | 2002-02-20 |
| ATE446124T1 (de) | 2009-11-15 |
| EP1187598B1 (de) | 2009-10-21 |
| EP1187598A1 (de) | 2002-03-20 |
| BR0011766A (pt) | 2002-03-05 |
| AU6262600A (en) | 2001-01-09 |
| AU778175B2 (en) | 2004-11-18 |
| JP4744754B2 (ja) | 2011-08-10 |
| MXPA01013101A (es) | 2002-06-04 |
| US6746666B1 (en) | 2004-06-08 |
| CN1355686A (zh) | 2002-06-26 |
| KR100759240B1 (ko) | 2007-09-18 |
| DE50015768D1 (de) | 2009-12-03 |
| WO2000078277A1 (de) | 2000-12-28 |
| MX231178B (es) | 2005-10-10 |
| CN1221244C (zh) | 2005-10-05 |
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