NO312332B1 - Lysfiltrerende kosmetisk sammensetning og anvendelse av denne - Google Patents

Lysfiltrerende kosmetisk sammensetning og anvendelse av denne Download PDF

Info

Publication number: NO312332B1
Authority: NO; Norway
Prior art keywords: light; cosmetic composition; composition according; butyl; tert
Prior art date: 1997-08-05

Application number

NO19983581A

Other languages

English (en)

Norwegian (no)

Other versions

NO983581D0 (no

NO983581L (no

Inventor

Alain Bringhen

Hans Ulrich Gonzenbach

Magali Pochon

Dominique Sidrac

Original Assignee

Hoffmann La Roche

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.)

1997-08-05

Filing date

1998-08-04

Publication date

2002-04-29

1998-08-04 Application filed by Hoffmann La Roche filed Critical Hoffmann La Roche

1998-08-04 Publication of NO983581D0 publication Critical patent/NO983581D0/no

1999-02-08 Publication of NO983581L publication Critical patent/NO983581L/no

2002-04-29 Publication of NO312332B1 publication Critical patent/NO312332B1/no

Links

239000000203 mixture Substances 0.000 title claims abstract description 29
239000002537 cosmetic Substances 0.000 title claims abstract description 27
238000001914 filtration Methods 0.000 title claims abstract description 14
150000001875 compounds Chemical class 0.000 claims abstract description 30
230000005855 radiation Effects 0.000 claims abstract description 9
125000000217 alkyl group Chemical group 0.000 claims abstract description 7
239000003795 chemical substances by application Substances 0.000 claims description 16
-1 2-ethylhexyl Chemical group 0.000 claims description 11
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 11
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 10
238000010521 absorption reaction Methods 0.000 claims description 7
125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims description 5
230000004224 protection Effects 0.000 claims description 5
RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 claims description 4
HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 claims description 4
XNEFYCZVKIDDMS-UHFFFAOYSA-N avobenzone Chemical group C1=CC(OC)=CC=C1C(=O)CC(=O)C1=CC=C(C(C)(C)C)C=C1 XNEFYCZVKIDDMS-UHFFFAOYSA-N 0.000 claims description 4
125000001147 pentyl group Chemical group C(CCCC)* 0.000 claims description 4
229910052719 titanium Inorganic materials 0.000 claims description 4
239000010936 titanium Substances 0.000 claims description 4
239000011701 zinc Substances 0.000 claims description 4
229910052725 zinc Inorganic materials 0.000 claims description 4
239000012965 benzophenone Substances 0.000 claims description 3
150000008366 benzophenones Chemical class 0.000 claims description 3
DSSYKIVIOFKYAU-XCBNKYQSSA-N (R)-camphor Chemical class C1C[C@@]2(C)C(=O)C[C@@H]1C2(C)C DSSYKIVIOFKYAU-XCBNKYQSSA-N 0.000 claims description 2
HIPQTCQUXOFTFI-UHFFFAOYSA-N 2-methoxy-1,3-diphenylpropane-1,3-dione Chemical compound C=1C=CC=CC=1C(=O)C(OC)C(=O)C1=CC=CC=C1 HIPQTCQUXOFTFI-UHFFFAOYSA-N 0.000 claims description 2
229910052684 Cerium Inorganic materials 0.000 claims description 2
QCWXUUIWCKQGHC-UHFFFAOYSA-N Zirconium Chemical compound [Zr] QCWXUUIWCKQGHC-UHFFFAOYSA-N 0.000 claims description 2
239000006096 absorbing agent Substances 0.000 claims description 2
235000010290 biphenyl Nutrition 0.000 claims description 2
239000004305 biphenyl Substances 0.000 claims description 2
ZMIGMASIKSOYAM-UHFFFAOYSA-N cerium Chemical compound [Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce] ZMIGMASIKSOYAM-UHFFFAOYSA-N 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
229910044991 metal oxide Inorganic materials 0.000 claims description 2
ZUOUZKKEUPVFJK-UHFFFAOYSA-N phenylbenzene Natural products C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 claims description 2
229920000642 polymer Polymers 0.000 claims description 2
150000003873 salicylate salts Chemical class 0.000 claims description 2
150000003918 triazines Chemical class 0.000 claims description 2
229910052726 zirconium Inorganic materials 0.000 claims description 2
YPFNIPKMNMDDDB-UHFFFAOYSA-K 2-[2-[bis(carboxylatomethyl)amino]ethyl-(2-hydroxyethyl)amino]acetate;iron(3+) Chemical compound [Fe+3].OCCN(CC([O-])=O)CCN(CC([O-])=O)CC([O-])=O YPFNIPKMNMDDDB-UHFFFAOYSA-K 0.000 claims 1
125000001183 hydrocarbyl group Chemical group 0.000 claims 1
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 21
KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 15
KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 15
239000003921 oil Substances 0.000 description 13
238000002360 preparation method Methods 0.000 description 10
XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 9
238000003756 stirring Methods 0.000 description 9
239000004808 2-ethylhexylester Substances 0.000 description 8
239000000839 emulsion Substances 0.000 description 7
239000007787 solid Substances 0.000 description 7
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 7
239000004904 UV filter Substances 0.000 description 6
238000009472 formulation Methods 0.000 description 5
YIWUKEYIRIRTPP-UHFFFAOYSA-N 2-ethylhexan-1-ol Chemical compound CCCCC(CC)CO YIWUKEYIRIRTPP-UHFFFAOYSA-N 0.000 description 4
150000002148 esters Chemical class 0.000 description 4
239000006210 lotion Substances 0.000 description 4
238000002844 melting Methods 0.000 description 4
230000008018 melting Effects 0.000 description 4
239000011541 reaction mixture Substances 0.000 description 4
ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
239000008407 cosmetic solvent Substances 0.000 description 3
239000006071 cream Substances 0.000 description 3
RHFZTBSULNJWEI-UHFFFAOYSA-N dimethyl 2-(methoxymethylidene)propanedioate Chemical compound COC=C(C(=O)OC)C(=O)OC RHFZTBSULNJWEI-UHFFFAOYSA-N 0.000 description 3
239000000499 gel Substances 0.000 description 3
VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
239000002904 solvent Substances 0.000 description 3
BJRXGOFKVBOFCO-UHFFFAOYSA-N 2-hydroxypropyl 16-methylheptadecanoate Chemical compound CC(C)CCCCCCCCCCCCCCC(=O)OCC(C)O BJRXGOFKVBOFCO-UHFFFAOYSA-N 0.000 description 2
VGUWZCUCNQXGBU-UHFFFAOYSA-N 3-[(4-methylpiperazin-1-yl)methyl]-5-nitro-1h-indole Chemical compound C1CN(C)CCN1CC1=CNC2=CC=C([N+]([O-])=O)C=C12 VGUWZCUCNQXGBU-UHFFFAOYSA-N 0.000 description 2
PLIKAWJENQZMHA-UHFFFAOYSA-N 4-aminophenol Chemical compound NC1=CC=C(O)C=C1 PLIKAWJENQZMHA-UHFFFAOYSA-N 0.000 description 2
HBTAOSGHCXUEKI-UHFFFAOYSA-N 4-chloro-n,n-dimethyl-3-nitrobenzenesulfonamide Chemical compound CN(C)S(=O)(=O)C1=CC=C(Cl)C([N+]([O-])=O)=C1 HBTAOSGHCXUEKI-UHFFFAOYSA-N 0.000 description 2
PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 2
AMQJEAYHLZJPGS-UHFFFAOYSA-N N-Pentanol Chemical compound CCCCCO AMQJEAYHLZJPGS-UHFFFAOYSA-N 0.000 description 2
239000002253 acid Substances 0.000 description 2
230000032683 aging Effects 0.000 description 2
150000001298 alcohols Chemical class 0.000 description 2
PWEOPMBMTXREGV-UHFFFAOYSA-N decanoic acid;octanoic acid;propane-1,2-diol Chemical compound CC(O)CO.CCCCCCCC(O)=O.CCCCCCCC(O)=O.CCCCCCCCCC(O)=O.CCCCCCCCCC(O)=O PWEOPMBMTXREGV-UHFFFAOYSA-N 0.000 description 2
229940031578 diisopropyl adipate Drugs 0.000 description 2
239000006185 dispersion Substances 0.000 description 2
DLAHAXOYRFRPFQ-UHFFFAOYSA-N dodecyl benzoate Chemical compound CCCCCCCCCCCCOC(=O)C1=CC=CC=C1 DLAHAXOYRFRPFQ-UHFFFAOYSA-N 0.000 description 2
230000000694 effects Effects 0.000 description 2
239000003480 eluent Substances 0.000 description 2
238000003818 flash chromatography Methods 0.000 description 2
235000013336 milk Nutrition 0.000 description 2
210000004080 milk Anatomy 0.000 description 2
BHAAPTBBJKJZER-UHFFFAOYSA-N p-anisidine Chemical compound COC1=CC=C(N)C=C1 BHAAPTBBJKJZER-UHFFFAOYSA-N 0.000 description 2
239000000049 pigment Substances 0.000 description 2
229920005862 polyol Polymers 0.000 description 2
150000003077 polyols Chemical class 0.000 description 2
BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 2
239000002453 shampoo Substances 0.000 description 2
239000007921 spray Substances 0.000 description 2
UFTFJSFQGQCHQW-UHFFFAOYSA-N triformin Chemical compound O=COCC(OC=O)COC=O UFTFJSFQGQCHQW-UHFFFAOYSA-N 0.000 description 2
239000007762 w/o emulsion Substances 0.000 description 2
239000001993 wax Substances 0.000 description 2
125000004209 (C1-C8) alkyl group Chemical group 0.000 description 1
OVYMWJFNQQOJBU-UHFFFAOYSA-N 1-octanoyloxypropan-2-yl octanoate Chemical compound CCCCCCCC(=O)OCC(C)OC(=O)CCCCCCC OVYMWJFNQQOJBU-UHFFFAOYSA-N 0.000 description 1
RMFFCSRJWUBPBJ-UHFFFAOYSA-N 15-hydroxypentadecyl benzoate Chemical compound OCCCCCCCCCCCCCCCOC(=O)C1=CC=CC=C1 RMFFCSRJWUBPBJ-UHFFFAOYSA-N 0.000 description 1
NFIHXTUNNGIYRF-UHFFFAOYSA-N 2-decanoyloxypropyl decanoate Chemical compound CCCCCCCCCC(=O)OCC(C)OC(=O)CCCCCCCCC NFIHXTUNNGIYRF-UHFFFAOYSA-N 0.000 description 1
SDQVYUNYDAWYIK-UHFFFAOYSA-N 2-oxobut-3-enal Chemical compound C=CC(=O)C=O SDQVYUNYDAWYIK-UHFFFAOYSA-N 0.000 description 1
IMPPGHMHELILKG-UHFFFAOYSA-N 4-ethoxyaniline Chemical compound CCOC1=CC=C(N)C=C1 IMPPGHMHELILKG-UHFFFAOYSA-N 0.000 description 1
ZDQWESQEGGJUCH-UHFFFAOYSA-N Diisopropyl adipate Chemical compound CC(C)OC(=O)CCCCC(=O)OC(C)C ZDQWESQEGGJUCH-UHFFFAOYSA-N 0.000 description 1
206010015150 Erythema Diseases 0.000 description 1
208000000453 Skin Neoplasms Diseases 0.000 description 1
230000006750 UV protection Effects 0.000 description 1
230000037338 UVA radiation Effects 0.000 description 1
239000002671 adjuvant Substances 0.000 description 1
239000000443 aerosol Substances 0.000 description 1
150000001448 anilines Chemical class 0.000 description 1
238000005282 brightening Methods 0.000 description 1
KMGBZBJJOKUPIA-UHFFFAOYSA-N butyl iodide Chemical compound CCCCI KMGBZBJJOKUPIA-UHFFFAOYSA-N 0.000 description 1
238000006243 chemical reaction Methods 0.000 description 1
239000003638 chemical reducing agent Substances 0.000 description 1
238000007796 conventional method Methods 0.000 description 1
STORWMDPIHOSMF-UHFFFAOYSA-N decanoic acid;octanoic acid;propane-1,2,3-triol Chemical compound OCC(O)CO.CCCCCCCC(O)=O.CCCCCCCCCC(O)=O STORWMDPIHOSMF-UHFFFAOYSA-N 0.000 description 1
230000018109 developmental process Effects 0.000 description 1
235000014113 dietary fatty acids Nutrition 0.000 description 1
LTMHNWPUDSTBKD-UHFFFAOYSA-N diethyl 2-(ethoxymethylidene)propanedioate Chemical compound CCOC=C(C(=O)OCC)C(=O)OCC LTMHNWPUDSTBKD-UHFFFAOYSA-N 0.000 description 1
239000000975 dye Substances 0.000 description 1
HEAHZSUCFKFERC-UHFFFAOYSA-N ecamsule Chemical compound CC1(C)C2CCC1(CS(O)(=O)=O)C(=O)C2=CC(C=C1)=CC=C1C=C1C(=O)C2(CS(O)(=O)=O)CCC1C2(C)C HEAHZSUCFKFERC-UHFFFAOYSA-N 0.000 description 1
239000003974 emollient agent Substances 0.000 description 1
239000003995 emulsifying agent Substances 0.000 description 1
231100000321 erythema Toxicity 0.000 description 1
OAYLNYINCPYISS-UHFFFAOYSA-N ethyl acetate;hexane Chemical compound CCCCCC.CCOC(C)=O OAYLNYINCPYISS-UHFFFAOYSA-N 0.000 description 1
238000011156 evaluation Methods 0.000 description 1
238000000605 extraction Methods 0.000 description 1
239000000194 fatty acid Substances 0.000 description 1
229930195729 fatty acid Natural products 0.000 description 1
150000004665 fatty acids Chemical class 0.000 description 1
150000002191 fatty alcohols Chemical class 0.000 description 1
239000006260 foam Substances 0.000 description 1
235000011187 glycerol Nutrition 0.000 description 1
125000003187 heptyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
239000003906 humectant Substances 0.000 description 1
150000002430 hydrocarbons Chemical group 0.000 description 1
229910052742 iron Inorganic materials 0.000 description 1
125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
239000004922 lacquer Substances 0.000 description 1
150000002632 lipids Chemical class 0.000 description 1
229910052943 magnesium sulfate Inorganic materials 0.000 description 1
235000019341 magnesium sulphate Nutrition 0.000 description 1
238000004519 manufacturing process Methods 0.000 description 1
239000000463 material Substances 0.000 description 1
SOXAGEOHPCXXIO-DVOMOZLQSA-N menthyl anthranilate Chemical compound CC(C)[C@@H]1CC[C@@H](C)C[C@H]1OC(=O)C1=CC=CC=C1N SOXAGEOHPCXXIO-DVOMOZLQSA-N 0.000 description 1
229960002248 meradimate Drugs 0.000 description 1
239000008267 milk Substances 0.000 description 1
125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
239000007764 o/w emulsion Substances 0.000 description 1
WWZKQHOCKIZLMA-UHFFFAOYSA-N octanoic acid Chemical compound CCCCCCCC(O)=O WWZKQHOCKIZLMA-UHFFFAOYSA-N 0.000 description 1
235000019645 odor Nutrition 0.000 description 1
239000002674 ointment Substances 0.000 description 1
239000012044 organic layer Substances 0.000 description 1
229920001296 polysiloxane Polymers 0.000 description 1
229910000027 potassium carbonate Inorganic materials 0.000 description 1
239000000843 powder Substances 0.000 description 1
239000003755 preservative agent Substances 0.000 description 1
239000003380 propellant Substances 0.000 description 1
230000001681 protective effect Effects 0.000 description 1
238000000746 purification Methods 0.000 description 1
230000001105 regulatory effect Effects 0.000 description 1
201000000849 skin cancer Diseases 0.000 description 1
239000011343 solid material Substances 0.000 description 1
239000000243 solution Substances 0.000 description 1
239000000126 substance Substances 0.000 description 1
230000000475 sunscreen effect Effects 0.000 description 1
239000000516 sunscreening agent Substances 0.000 description 1
239000004094 surface-active agent Substances 0.000 description 1
239000000725 suspension Substances 0.000 description 1
125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
239000002562 thickening agent Substances 0.000 description 1
VXUYXOFXAQZZMF-UHFFFAOYSA-N titanium(IV) isopropoxide Chemical compound CC(C)O[Ti](OC(C)C)(OC(C)C)OC(C)C VXUYXOFXAQZZMF-UHFFFAOYSA-N 0.000 description 1
239000002966 varnish Substances 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
- A61K8/30—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
- A61K8/40—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing nitrogen
- 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
- A61K8/40—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing nitrogen
- A61K8/44—Aminocarboxylic acids or derivatives thereof, e.g. aminocarboxylic acids containing sulfur; Salts; Esters or N-acylated derivatives thereof
- 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

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)
Emergency Medicine (AREA)
Cosmetics (AREA)

NO19983581A 1997-08-05 1998-08-04 Lysfiltrerende kosmetisk sammensetning og anvendelse av denne NO312332B1 (no)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
EP97113446		1997-08-05

Publications (3)

Publication Number	Publication Date
NO983581D0 NO983581D0 (no)	1998-08-04
NO983581L NO983581L (no)	1999-02-08
NO312332B1 true NO312332B1 (no)	2002-04-29

Family

ID=8227170

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
NO19983581A NO312332B1 (no)	1997-08-05	1998-08-04	Lysfiltrerende kosmetisk sammensetning og anvendelse av denne

Country Status (14)

Country	Link
US (1)	US6069170A (id)
EP (1)	EP0895776B1 (id)
JP (1)	JPH11100318A (id)
KR (1)	KR100543269B1 (id)
CN (1)	CN1148165C (id)
AU (1)	AU739558B2 (id)
BR (1)	BR9802837A (id)
CA (1)	CA2244556A1 (id)
DE (1)	DE69815449T2 (id)
DK (1)	DK0895776T3 (id)
ES (1)	ES2198026T3 (id)
ID (1)	ID20678A (id)
NO (1)	NO312332B1 (id)
TW (1)	TW516965B (id)

Families Citing this family (59)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE19904329A1 (de) *	1999-01-28	2000-08-03	Cognis Deutschland Gmbh	Kosmetische und/oder pharmazeutische Zubereitungen
US6165451A (en) *	1999-02-08	2000-12-26	Roche Vitamins Inc.	Cosmetic light screening composition
EP1025836A1 (en) *	1999-02-08	2000-08-09	F. Hoffmann-La Roche Ag	Cosmetic light screening composition
DE19937299A1 (de) *	1999-08-06	2001-02-15	Cognis Deutschland Gmbh	Sonnenschutzmittel
DE10063946A1 (de)	2000-12-20	2002-07-04	Basf Ag	Verwendung von Lichtschutzmittelkombinationen, die als wesentlichen Bestandteil 2,2'-p-Phenylen-bis(3,1-benzoxazin-4-on) enthalten als photostabile UV-Filter in kosmetischen und pharmazeutischen Zubereitungen
DE10063867A1 (de) *	2000-12-21	2002-07-11	Haarmann & Reimer Gmbh	Kosmetische Lichtschutzzubereitungen
DE10113058A1 (de)	2001-03-15	2002-09-19	Basf Ag	Verwendung von Lichtschutzmittelkombinationen, die als wesentlichen Bestandteil 2-(4-Alkoxy-anilinomethylen)-malonsäure-dialkylester enthalten als photostabile UV-Filter in kosmetischen und pharmazeutischen Zubereitungen
DE10124332A1 (de)	2001-05-18	2002-11-21	Basf Ag	Kosmetische oder pharmazeutische Zubereitungen, die Enaminotriazine als Lichtschutzmittel enthalten und neue Enaminotriazine
DE10143960A1 (de) *	2001-09-07	2003-03-27	Basf Ag	Kosmetische und dermatologische Zubereitungen in Stiftform, enthaltend ein aminosubstituiertes Hydroxybenzophenon
DE10143962A1 (de) *	2001-09-07	2003-03-27	Basf Ag	Kosmetische und dermatologische Zubereitungen in Form von O/W-Emulsionen, enthaltend ein aminosubstituiertes Hydroxybenzophenon
DE10143963A1 (de) *	2001-09-07	2003-03-27	Basf Ag	Kosmetische und dermatologische Zubereitungen in Form von W/O-Emulsionen, enthaltend ein aminosubstituiertes Hydroxybenzophenon
DE10143964A1 (de) *	2001-09-07	2003-03-27	Basf Ag	Emulgatorarme oder emulgatorfreie Systeme vom Typ Öl-in-Wasser mit einem Gehalt an Stabilisatoren und einem aminosubstituierten Hydroxybenzophenon
JP4369203B2 (ja) *	2003-03-24	2009-11-18	信越化学工業株式会社	反射防止膜材料、反射防止膜を有する基板及びパターン形成方法
KR100857967B1 (ko) *	2003-06-03	2008-09-10	신에쓰 가가꾸 고교 가부시끼가이샤	반사 방지막 재료, 이것을 이용한 반사 방지막 및 패턴형성 방법
KR100882409B1 (ko) *	2003-06-03	2009-02-05	신에쓰 가가꾸 고교 가부시끼가이샤	반사 방지용 실리콘 수지, 반사 방지막 재료, 이것을 이용한 반사 방지막 및 패턴 형성 방법
US20070190325A1 (en)	2003-12-04	2007-08-16	Katja Berg-Schultz	Microcapsules with uv filter activity and process for producing them
JP5031551B2 (ja)	2004-03-25	2012-09-19	ディーエスエムアイピーアセッツビー．ブイ．	化粧品組成物
EP1727516B1 (en)	2004-03-26	2014-05-14	DSM IP Assets B.V.	Composition comprising an hdac inhibitor in combination with a retinoid
ATE551048T1 (de)	2004-06-28	2012-04-15	Dsm Ip Assets Bv	Proteinhydrolysate enthaltende kosmetische zusammensetzungen
US20080031909A1 (en)	2004-12-10	2008-02-07	Dsm Ip Assets B.V.	Encapsulated Cosmetic Materials
US20090041813A1 (en)	2005-02-21	2009-02-12	Basf Aktiengesellschaft	Active substance composition comprising at least one nitrogen atom-containing, hyperbranched polymer
EP1926703B1 (en)	2005-09-20	2013-01-09	DSM IP Assets B.V.	Novel carboxylic acid derivatives
EP1959914B1 (en)	2005-12-09	2014-05-21	DSM IP Assets B.V.	Cosmetic or dermatological compositions comprising modified titanium dioxide particles
JP5176188B2 (ja)	2006-04-21	2013-04-03	ディーエスエムアイピーアセッツビー．ブイ．	オピオイド受容体拮抗薬の使用
EP2032115B1 (en)	2006-06-16	2021-07-21	DSM IP Assets B.V.	Compositions based on hyperbranched condensation polymers and novel hyperbranched condensation polymers
CN101516386B (zh)	2006-07-14	2013-05-15	帝斯曼知识产权资产管理有限公司	包含玫瑰果和其它活性剂的用于治疗炎性病症的组合物
WO2009038463A1 (en)	2007-09-18	2009-03-26	Fujifilm Manufacturing Europe B.V.	Uv absorbing compounds
EP2070525A1 (en)	2007-12-11	2009-06-17	DSM IP Assets B.V.	Compositions comprising Magnolol and/or Honokiol and chondroitin and use thereof for the treatment, co-treatment or prevention of inflammatory disorders
EP2070524A1 (en)	2007-12-11	2009-06-17	DSM IP Assets B.V.	Compositions comprising Magnolol and/or Honokiol and glucosamine and use thereof for the treatment, co-treatment or prevention of inflammatory disorders
KR20110120334A (ko)	2009-02-23	2011-11-03	디에스엠 아이피 어셋츠 비.브이.	염증성 질환용 카자누스 추출물 및 글루코사민
US20120282200A1 (en)	2009-12-09	2012-11-08	Alexander Schlifke-Poschalko	Uv absorbing dentritic polyether prepared by polymerization of oxetanes
WO2011070068A2 (en)	2009-12-09	2011-06-16	Dsm Ip Assets B.V.	Novel compounds
EP2509576B1 (en)	2009-12-09	2014-08-27	DSM IP Assets B.V.	Polyglycerol based UV filter comprising p-dimethylamino benzoate
WO2011070075A2 (en)	2009-12-09	2011-06-16	Dsm Ip Assets B.V.	Novel compounds
US20130004437A1 (en)	2009-12-09	2013-01-03	Alexander Schlifke-Poschalko	Novel compound
EP2509579B1 (en)	2009-12-09	2014-09-03	DSM IP Assets B.V.	Novel compound
CN102655849B (zh)	2009-12-09	2015-04-15	帝斯曼知识产权资产管理有限公司	新颖的化合物
CN102791698B (zh)	2010-01-15	2014-11-12	帝斯曼知识产权资产管理有限公司	用于uv辐射吸收的2-苯基-1，2，3-苯并三唑
WO2011121093A1 (en)	2010-03-31	2011-10-06	Dsm Ip Assets B.V.	Use of organic compounds in hair care
US9445979B2 (en)	2010-04-12	2016-09-20	Dsm Ip Assets B.V.	Hair treatment composition containing gambogic acid, ester or amide
JP5850266B2 (ja)	2010-07-23	2016-02-03	ディーエスエムアイピーアセッツビー．ブイ．	ヘアケアにおけるステビオール又は誘導体の局所使用
US20140044656A1 (en)	2011-03-01	2014-02-13	Dsm Ip Assets B.V.	Novel use
EP2522331A1 (en)	2011-05-09	2012-11-14	DSM IP Assets B.V.	Use of resveratrol and niacinamide
EP2522329A1 (en)	2011-05-09	2012-11-14	DSM IP Assets B.V.	Use of resveratrol and arbutin
EP2522330A1 (en)	2011-05-09	2012-11-14	DSM IP Assets B.V.	Use of resveratrol and an edelweiss extract
EP2522335A1 (en)	2011-05-09	2012-11-14	DSM IP Assets B.V.	Use of resveratrol and sodium-ascorbyl-phophate
EP2522328A1 (en)	2011-05-09	2012-11-14	DSM IP Assets B.V.	Use of resveratrol and ascorbyl-2-glucoside
EP2522332A1 (en)	2011-05-09	2012-11-14	DSM IP Assets B.V.	Use of resveratrol and magnesium-ascorbyl-phosphate
WO2013041515A1 (en)	2011-09-20	2013-03-28	Dsm Ip Assets B.V.	Novel polyester based uv filters
CN104039301A (zh)	2012-01-09	2014-09-10	帝斯曼知识产权资产管理有限公司	丹涅酮及其衍生物在皮肤护理中的用途
EP2623094A1 (en)	2012-02-02	2013-08-07	DSM IP Assets B.V.	Use of an edelweiss extract
WO2015049366A1 (en)	2013-10-04	2015-04-09	Dsm Ip Assets B.V.	Skin tanning extract
EP2873440A1 (en)	2013-11-19	2015-05-20	DSM IP Assets B.V.	Use of an edelweiss extract in hair care for stimulating hair growth
EP2873414A1 (en)	2013-11-19	2015-05-20	DSM IP Assets B.V.	Use of an edelweiss extract in hair care for the prevention of hair graying
KR102487937B1 (ko)	2014-10-17	2023-01-13	디에스엠 아이피 어셋츠 비.브이.	10-하이드록시스테아르산을 포함하는 화장품 조성물의 용도
KR102623466B1 (ko)	2014-12-04	2024-01-09	루브리졸 어드밴스드 머티어리얼스, 인코포레이티드	유기 상 함유 조성물의 점도 개질
JP6796949B2 (ja) *	2016-05-23	2020-12-09	花王株式会社	水中油型乳化化粧料の製造方法
EP3421096A1 (en)	2017-06-30	2019-01-02	Athenion AG	Method for solubilizing poorly water-soluble cosmetic agents
EP3709956B1 (en)	2017-11-13	2024-10-23	DSM IP Assets B.V.	Cosmetic or dermatological compositions

Family Cites Families (9)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
NL279734A (id) *	1961-06-26
US3515745A (en) *	1967-10-05	1970-06-02	Merck & Co Inc	Synthesis of arylamino methylenemalonates
DE1908548A1 (de) *	1968-02-29	1970-11-05	Warner Lambert Co	Chinolinderivate
NL190101C (nl) *	1978-11-13	1993-11-01	Givaudan & Cie Sa	Dibenzoylmethaanverbinding en tegen licht beschermend preparaat.
GB8422916D0 (en) *	1984-09-11	1984-10-17	May & Baker Ltd	Compositions of matter
GB9110123D0 (en) *	1991-05-10	1991-07-03	Dow Corning	Organosilicon compounds their preparation and use
DE4122475A1 (de) *	1991-07-06	1993-01-07	Basf Ag	Aminomethylencyanessigester
DE59510031D1 (de) *	1994-11-10	2002-03-14	Basf Ag	2-Cyanacrylsäureester
US5639446A (en) *	1996-09-20	1997-06-17	3V Inc.	Derivatives of benzoxazole useful as UV stabilizers

1998
- 1998-07-24 US US09/122,117 patent/US6069170A/en not_active Expired - Fee Related
- 1998-07-30 DK DK98114262T patent/DK0895776T3/da active
- 1998-07-30 CA CA002244556A patent/CA2244556A1/en not_active Abandoned
- 1998-07-30 EP EP98114262A patent/EP0895776B1/en not_active Expired - Lifetime
- 1998-07-30 DE DE69815449T patent/DE69815449T2/de not_active Expired - Fee Related
- 1998-07-30 ES ES98114262T patent/ES2198026T3/es not_active Expired - Lifetime
- 1998-08-03 CN CNB981167918A patent/CN1148165C/zh not_active Expired - Fee Related
- 1998-08-04 NO NO19983581A patent/NO312332B1/no not_active IP Right Cessation
- 1998-08-04 AU AU78776/98A patent/AU739558B2/en not_active Ceased
- 1998-08-04 JP JP10219930A patent/JPH11100318A/ja active Pending
- 1998-08-04 KR KR1019980031729A patent/KR100543269B1/ko not_active Expired - Fee Related
- 1998-08-04 ID IDP981090A patent/ID20678A/id unknown
- 1998-08-04 BR BR9802837-5A patent/BR9802837A/pt not_active Application Discontinuation
- 1998-10-01 TW TW087116339A patent/TW516965B/zh not_active IP Right Cessation

Also Published As

Publication number	Publication date
EP0895776A3 (en)	1999-04-28
CA2244556A1 (en)	1999-02-05
NO983581D0 (no)	1998-08-04
KR100543269B1 (ko)	2006-04-21
US6069170A (en)	2000-05-30
ID20678A (id)	1999-02-11
AU7877698A (en)	1999-02-18
EP0895776B1 (en)	2003-06-11
TW516965B (en)	2003-01-11
NO983581L (no)	1999-02-08
KR19990023356A (ko)	1999-03-25
CN1207290A (zh)	1999-02-10
AU739558B2 (en)	2001-10-18
DK0895776T3 (da)	2003-08-25
ES2198026T3 (es)	2004-01-16
CN1148165C (zh)	2004-05-05
EP0895776A2 (en)	1999-02-10
JPH11100318A (ja)	1999-04-13
DE69815449T2 (de)	2004-02-12
BR9802837A (pt)	2000-01-11
DE69815449D1 (de)	2003-07-17

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Date	Code	Title	Description
2005-05-02	MM1K	Lapsed by not paying the annual fees

Publication	Publication Date	Title
NO312332B1 (no)	2002-04-29	Lysfiltrerende kosmetisk sammensetning og anvendelse av denne
JP3083905B2 (ja)	2000-09-04	ベンジリデンカンファー置換基を有するｓ−トリアジン誘導体、その製造方法、および化粧品組成物
EP0507691B1 (fr)	1995-03-15	Dérivés s-triaziniques portant des substituants benzalmalonates, leur procédé de préparation, compositions cosmétiques filtrantes les contenant et leur utilisation pour protéger la peau et les cheveux du rayonnement ultraviolet
CA1204779A (fr)	1986-05-20	3-benzylidene camphres, leur procede de preparation et leur utilisation pour la protection contre les rayons uv
US5783173A (en)	1998-07-21	Stable sunscreen composition containing dibenzoylmethane derivative, E. G., PARSOL 1789, and C12, C16, C18, branched chain hydroxybenzoate and/or C12, C16, branched chain benzoate stabilizers/solubilizers
KR100512508B1 (ko)	2006-01-27	인다닐리덴화합물,그의제조방법및자외선흡수제로서이들의용도
EP1990372A2 (en)	2008-11-12	Water soluble UV filters
AU622195B2 (en)	1992-04-02	New liposoluble unsaturated benzalmalonate derivatives and their use as absorbers for ultraviolet radiation in cosmetics
US5776439A (en)	1998-07-07	Sun protecting cosmetic compositions comprising derivatives of dibenzoylmethane and of benzophenone
CN102448429B (zh)	2018-03-06	亚苄基丙二酸酯
AU2005288930B2 (en)	2011-06-23	Photo-stable cosmetic or dermatological compositions
CA2989120C (en)	2020-10-06	Solubilizing agents for functional uv active compounds
DE69718664T2 (de)	2003-06-12	Verwendung von selektierten benzotriazol derivaten zum schutz von menschlicher und tierischer haut und haar vor der schädigenden einwirkung von uv-strahlung
EP4110754A1 (en)	2023-01-04	Process for isolating 2-(4'-diethylamino-2'-hydroxybenzoyl)benzoic acid hexyl ester
EP0891766A1 (en)	1999-01-20	Light-screening agents
DE602004007181T2 (de)	2008-02-28	2,4,6-Tris(dineopentyl-4'-amino-benzalmalonat)-s-triazin, kosmetische Lichtschutzmittel, die diese Verbindung enthalten, und Verwendung dieser Verbindung
GB2211844A (en)	1989-07-12	New benzylidenecamphor sulphonamides
JP3686911B2 (ja)	2005-08-24	ベンジリデン−γ−ブチロラクトン、それらの調製法及びＵＶ吸収剤としてのそれらの使用法
DE602005001872T2 (de)	2008-05-08	s-Triazinderivate, die mindestens zwei p-Aminobenzalmalonatsilangruppen enthalten; kosmetische Lichtschutzzusammensetzungen, die diese Derivate enthalten; und Verwendungen der s-Triazinderivate
MXPA98006282A (en)	1999-09-20	Cosmetic composition filter of the
EP1466908A1 (fr)	2004-10-13	Nouveaux dérivés de s-triazine possédant au moins un sel d'acide para-amino benzalmalonique greffé et compositions cosmétique photoprotectrices contenant ces dérivés
EP0969004B1 (en)	2003-12-10	2,4,6-Trianilino-1,3,5-triazine derivatives, their preparation and their use as sunscreens against UV-B sun radiations
JP2002053527A (ja)	2002-02-19	５，５−ジアリール−２，４−ペンタジエン酸エステル系化合物および該化合物を有効成分とする紫外線吸収剤
WO2003084496A1 (de)	2003-10-16	Lichtschutzzubereitungen mit lichtstabilem uv-a schutz