NO312992B1 - Anvendelse av <alfa>1<alfa>-dicyano-<beta>1<beta>- difenyletylenforbindelser til fotostabilisering av dibenzoylmetantype UV-A beskyttelsesmidler - Google Patents

Anvendelse av <alfa>1<alfa>-dicyano-<beta>1<beta>- difenyletylenforbindelser til fotostabilisering av dibenzoylmetantype UV-A beskyttelsesmidler Download PDF

Info

Publication number: NO312992B1
Authority: NO; Norway
Prior art keywords: use according; tert; butyl; dibenzoylmethane; formula
Prior art date: 1997-07-14

Application number

NO19983112A

Other languages

English (en)

Norwegian (no)

Other versions

NO983112L (no

Inventor

Alain Bringhen

Hans Ulrich Gonzenbach

Magali Pochon

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.)

1997-07-14

Filing date

1998-07-06

Publication date

2002-07-29

1998-07-06 Application filed by Hoffmann La Roche filed Critical Hoffmann La Roche

1999-01-15 Publication of NO983112L publication Critical patent/NO983112L/no

2002-07-29 Publication of NO312992B1 publication Critical patent/NO312992B1/no

Links

239000003223 protective agent Substances 0.000 title claims description 20
NZZIMKJIVMHWJC-UHFFFAOYSA-N dibenzoylmethane Chemical compound C=1C=CC=CC=1C(=O)CC(=O)C1=CC=CC=C1 NZZIMKJIVMHWJC-UHFFFAOYSA-N 0.000 title claims description 13
230000000176 photostabilization Effects 0.000 title claims description 10
150000001875 compounds Chemical class 0.000 claims description 43
-1 n-propoxy- Chemical class 0.000 claims description 41
239000000203 mixture Substances 0.000 claims description 24
239000002537 cosmetic Substances 0.000 claims description 15
239000003795 chemical substances by application Substances 0.000 claims description 14
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 10
XNEFYCZVKIDDMS-UHFFFAOYSA-N avobenzone Chemical compound C1=CC(OC)=CC=C1C(=O)CC(=O)C1=CC=C(C(C)(C)C)C=C1 XNEFYCZVKIDDMS-UHFFFAOYSA-N 0.000 claims description 9
230000005855 radiation Effects 0.000 claims description 7
XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims description 6
RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 claims description 6
HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 claims description 6
239000000463 material Substances 0.000 claims description 6
229910052719 titanium Inorganic materials 0.000 claims description 6
239000010936 titanium Substances 0.000 claims description 6
239000011701 zinc Substances 0.000 claims description 6
229910052725 zinc Inorganic materials 0.000 claims description 6
125000004432 carbon atom Chemical group C* 0.000 claims description 5
239000000049 pigment Substances 0.000 claims description 5
125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims description 5
229920000642 polymer Polymers 0.000 claims description 4
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 3
229910052684 Cerium Inorganic materials 0.000 claims description 3
QCWXUUIWCKQGHC-UHFFFAOYSA-N Zirconium Chemical compound [Zr] QCWXUUIWCKQGHC-UHFFFAOYSA-N 0.000 claims description 3
125000000217 alkyl group Chemical group 0.000 claims description 3
239000012965 benzophenone Substances 0.000 claims description 3
150000008366 benzophenones Chemical class 0.000 claims description 3
235000010290 biphenyl Nutrition 0.000 claims description 3
239000004305 biphenyl Substances 0.000 claims description 3
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 3
WBYWAXJHAXSJNI-UHFFFAOYSA-N cinnamic acid Chemical class OC(=O)C=CC1=CC=CC=C1 WBYWAXJHAXSJNI-UHFFFAOYSA-N 0.000 claims description 3
229910052742 iron Inorganic materials 0.000 claims description 3
229910044991 metal oxide Inorganic materials 0.000 claims description 3
ZUOUZKKEUPVFJK-UHFFFAOYSA-N phenylbenzene Natural products C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 claims description 3
150000003873 salicylate salts Chemical class 0.000 claims description 3
229910052726 zirconium Inorganic materials 0.000 claims description 3
125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 2
239000003755 preservative agent Substances 0.000 claims description 2
239000000126 substance Substances 0.000 claims description 2
125000006606 n-butoxy group Chemical group 0.000 claims 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 1
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims 1
230000002335 preservative effect Effects 0.000 claims 1
238000009472 formulation Methods 0.000 description 8
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 7
230000006641 stabilisation Effects 0.000 description 5
238000011105 stabilization Methods 0.000 description 5
239000003381 stabilizer Substances 0.000 description 5
239000000839 emulsion Substances 0.000 description 4
238000002474 experimental method Methods 0.000 description 4
238000000034 method Methods 0.000 description 4
229960000601 octocrylene Drugs 0.000 description 4
229920001296 polysiloxane Polymers 0.000 description 4
238000002360 preparation method Methods 0.000 description 4
239000002904 solvent Substances 0.000 description 4
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
230000000694 effects Effects 0.000 description 3
239000000499 gel Substances 0.000 description 3
150000004658 ketimines Chemical class 0.000 description 3
239000006210 lotion Substances 0.000 description 3
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 3
239000003921 oil Substances 0.000 description 3
230000000087 stabilizing effect Effects 0.000 description 3
229960000368 sulisobenzone Drugs 0.000 description 3
HIQIXEFWDLTDED-UHFFFAOYSA-N 4-hydroxy-1-piperidin-4-ylpyrrolidin-2-one Chemical compound O=C1CC(O)CN1C1CCNCC1 HIQIXEFWDLTDED-UHFFFAOYSA-N 0.000 description 2
PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 2
KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
150000001298 alcohols Chemical class 0.000 description 2
238000009835 boiling Methods 0.000 description 2
230000002596 correlated effect Effects 0.000 description 2
239000008407 cosmetic solvent Substances 0.000 description 2
239000006185 dispersion Substances 0.000 description 2
239000011521 glass Substances 0.000 description 2
238000004128 high performance liquid chromatography Methods 0.000 description 2
125000001183 hydrocarbyl group Chemical group 0.000 description 2
229910052739 hydrogen Inorganic materials 0.000 description 2
239000001257 hydrogen Substances 0.000 description 2
XUGNVMKQXJXZCD-UHFFFAOYSA-N isopropyl palmitate Chemical group CCCCCCCCCCCCCCCC(=O)OC(C)C XUGNVMKQXJXZCD-UHFFFAOYSA-N 0.000 description 2
229920005862 polyol Polymers 0.000 description 2
150000003077 polyols Chemical class 0.000 description 2
239000000047 product Substances 0.000 description 2
239000002453 shampoo Substances 0.000 description 2
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 2
239000002966 varnish Substances 0.000 description 2
239000001993 wax Substances 0.000 description 2
229910052724 xenon Inorganic materials 0.000 description 2
FHNFHKCVQCLJFQ-UHFFFAOYSA-N xenon atom Chemical compound [Xe] FHNFHKCVQCLJFQ-UHFFFAOYSA-N 0.000 description 2
LSHGMOIQPURPAK-UHFFFAOYSA-N 2-benzylidene-1,4,7,7-tetramethylbicyclo[2.2.1]heptan-3-one Chemical compound CC1(C)C(C2=O)(C)CCC1(C)C2=CC1=CC=CC=C1 LSHGMOIQPURPAK-UHFFFAOYSA-N 0.000 description 1
JXPDNDHCMMOJPC-UHFFFAOYSA-N 2-hydroxybutanedinitrile Chemical compound N#CC(O)CC#N JXPDNDHCMMOJPC-UHFFFAOYSA-N 0.000 description 1
ISDGWTZFJKFKMO-UHFFFAOYSA-N 2-phenyl-1,3-dioxane-4,6-dione Chemical compound O1C(=O)CC(=O)OC1C1=CC=CC=C1 ISDGWTZFJKFKMO-UHFFFAOYSA-N 0.000 description 1
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 1
239000007818 Grignard reagent Substances 0.000 description 1
FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
239000002250 absorbent Substances 0.000 description 1
230000002745 absorbent Effects 0.000 description 1
239000000443 aerosol Substances 0.000 description 1
239000002518 antifoaming agent Substances 0.000 description 1
125000000649 benzylidene group Chemical group [H]C(=[*])C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 1
244000309464 bull Species 0.000 description 1
238000004587 chromatography analysis Methods 0.000 description 1
238000001816 cooling Methods 0.000 description 1
230000000875 corresponding effect Effects 0.000 description 1
239000006071 cream Substances 0.000 description 1
235000014113 dietary fatty acids Nutrition 0.000 description 1
239000000975 dye Substances 0.000 description 1
239000003995 emulsifying agent Substances 0.000 description 1
150000002148 esters Chemical class 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
239000000706 filtrate Substances 0.000 description 1
238000001914 filtration Methods 0.000 description 1
239000006260 foam Substances 0.000 description 1
239000003205 fragrance Substances 0.000 description 1
235000011187 glycerol Nutrition 0.000 description 1
150000004795 grignard reagents Chemical class 0.000 description 1
150000004820 halides Chemical class 0.000 description 1
125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
239000003906 humectant Substances 0.000 description 1
125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
150000002632 lipids Chemical class 0.000 description 1
239000011777 magnesium Substances 0.000 description 1
229910052749 magnesium Inorganic materials 0.000 description 1
238000004519 manufacturing process Methods 0.000 description 1
239000008267 milk Substances 0.000 description 1
235000013336 milk Nutrition 0.000 description 1
210000004080 milk Anatomy 0.000 description 1
238000002156 mixing Methods 0.000 description 1
125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
150000002825 nitriles Chemical class 0.000 description 1
239000002245 particle Substances 0.000 description 1
125000001147 pentyl group Chemical group C(CCCC)* 0.000 description 1
230000000704 physical effect Effects 0.000 description 1
239000000843 powder Substances 0.000 description 1
230000002035 prolonged effect Effects 0.000 description 1
239000003380 propellant Substances 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
238000010992 reflux Methods 0.000 description 1
239000007921 spray Substances 0.000 description 1
238000003756 stirring Methods 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
239000002562 thickening agent 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
- 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
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q5/00—Preparations for care of the hair
- 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)
Animal Behavior & Ethology (AREA)
General Health & Medical Sciences (AREA)
Public Health (AREA)
Veterinary Medicine (AREA)
Birds (AREA)
Epidemiology (AREA)
Emergency Medicine (AREA)
Dermatology (AREA)
Cosmetics (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

NO19983112A 1997-07-14 1998-07-06 Anvendelse av <alfa>1<alfa>-dicyano-<beta>1<beta>- difenyletylenforbindelser til fotostabilisering av dibenzoylmetantype UV-A beskyttelsesmidler NO312992B1 (no)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
EP97111938		1997-07-14

Publications (2)

Publication Number	Publication Date
NO983112L NO983112L (no)	1999-01-15
NO312992B1 true NO312992B1 (no)	2002-07-29

Family

ID=8227058

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
NO19983112A NO312992B1 (no)	1997-07-14	1998-07-06	Anvendelse av <alfa>1<alfa>-dicyano-<beta>1<beta>- difenyletylenforbindelser til fotostabilisering av dibenzoylmetantype UV-A beskyttelsesmidler

Country Status (10)

Country	Link
US (1)	US6048516A (id)
EP (1)	EP0891766A1 (id)
JP (1)	JPH1171254A (id)
KR (1)	KR19990013804A (id)
CN (1)	CN1214239A (id)
AU (1)	AU735151B2 (id)
BR (1)	BR9802481A (id)
CA (1)	CA2241645A1 (id)
ID (1)	ID20577A (id)
NO (1)	NO312992B1 (id)

Families Citing this family (12)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US6440402B1 (en)	2001-12-14	2002-08-27	Avon Products, Inc.	Photostable sunscreen compositions and methods of stabilizing
JP4020680B2 (ja) *	2002-04-12	2007-12-12	株式会社ルネサステクノロジ	半導体集積回路
US7597825B2 (en) *	2007-08-09	2009-10-06	Hallstar Innovations Corp.	Method of quenching electronic excitation of chromophore-containing organic molecules in photoactive compositions
US7588702B2 (en) *	2007-08-09	2009-09-15	Hallstar Innovations Corp.	Method of quenching electronic excitation of chromophore-containing organic molecules in photoactive compositions
US9469725B2 (en)	2012-06-28	2016-10-18	Johnson & Johnson Consumer Inc.	Ultraviolet radiation absorbing polymers
US9255180B2 (en)	2012-06-28	2016-02-09	Johnson & Johnson Consumer Inc.	Ultraviolet radiation absorbing polyethers
US20140004057A1 (en)	2012-06-28	2014-01-02	Johnson & Johnson Consumer Companies, Inc.	Sunscreen compositions containing an ultraviolet radiation-absorbing polyester
CN104411367A (zh)	2012-06-28	2015-03-11	强生消费者公司	包含紫外线辐射吸收性聚合物的防晒剂组合物
US10874603B2 (en)	2014-05-12	2020-12-29	Johnson & Johnson Consumer Inc.	Sunscreen compositions containing a UV-absorbing polyglycerol and a non-UV-absorbing polyglycerol
WO2017218390A1 (en)	2016-06-16	2017-12-21	Johnson & Johnson Consumer Inc.	Sunscreen compositions containing a combination of a linear ultraviolet radiation-absorbing polyether and other ultraviolet-screening compounds
US10596087B2 (en)	2016-10-05	2020-03-24	Johnson & Johnson Consumer Inc.	Ultraviolet radiation absorbing polymer composition
JP2021024840A (ja) *	2019-08-08	2021-02-22	山田化学工業株式会社	色素化合物

Family Cites Families (10)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US3270045A (en) *	1961-03-23	1966-08-30	Gen Aniline & Film Corp	Diphenyl methylene-malononitrile compounds
US3275520A (en) *	1962-05-29	1966-09-27	Gen Aniline & Film Corp	Methods for protecting the skin against actinic radiations
NL190101C (nl) *	1978-11-13	1993-11-01	Givaudan & Cie Sa	Dibenzoylmethaanverbinding en tegen licht beschermend preparaat.
FR2658075B1 (fr) *	1990-02-14	1992-05-07	Oreal	Composition cosmetique filtrante photostable contenant un filtre uv-a et un beta,beta-diphenylacrylate ou alpha-cyano-beta,beta-diphenylacrylate d'alkyle.
GB9110123D0 (en) *	1991-05-10	1991-07-03	Dow Corning	Organosilicon compounds their preparation and use
ATE212536T1 (de) *	1994-10-14	2002-02-15	Hoffmann La Roche	Lichtstabile kosmetische sonnenschutzmittel
US5840282A (en) *	1995-06-21	1998-11-24	Givaudan-Roure (International) Sa	Light screening compositions
DE19540952A1 (de) *	1995-11-03	1997-05-07	Basf Ag	Photostabile UV-A-Filter enthaltende kosmetische Zubereitungen
FR2742048B1 (fr) *	1995-12-08	1998-01-09	Oreal	Utilisation de l'alpha-cyano-beta, beta-diphenylacrylate de 2-ethylhexyle pour ameliorer la stabilite de compositions cosmetiques contenant le p-methyl-benzylidene camphre en association avec un derive de dibenzoylmethane
US6033649A (en) *	1995-12-18	2000-03-07	Roche Vitamins Inc.	Light screening agents

1998
- 1998-06-24 CA CA002241645A patent/CA2241645A1/en not_active Abandoned
- 1998-06-30 AU AU73963/98A patent/AU735151B2/en not_active Ceased
- 1998-07-06 NO NO19983112A patent/NO312992B1/no not_active IP Right Cessation
- 1998-07-10 US US09/113,863 patent/US6048516A/en not_active Expired - Fee Related
- 1998-07-10 ID IDP980984A patent/ID20577A/id unknown
- 1998-07-13 BR BR9802481-7A patent/BR9802481A/pt not_active IP Right Cessation
- 1998-07-13 KR KR1019980028096A patent/KR19990013804A/ko not_active Withdrawn
- 1998-07-13 EP EP98112954A patent/EP0891766A1/en not_active Withdrawn
- 1998-07-14 CN CN98115991A patent/CN1214239A/zh active Pending
- 1998-07-14 JP JP10198345A patent/JPH1171254A/ja active Pending

Also Published As

Publication number	Publication date
EP0891766A1 (en)	1999-01-20
KR19990013804A (ko)	1999-02-25
JPH1171254A (ja)	1999-03-16
US6048516A (en)	2000-04-11
AU735151B2 (en)	2001-07-05
CA2241645A1 (en)	1999-01-14
BR9802481A (pt)	2000-02-08
NO983112L (no)	1999-01-15
CN1214239A (zh)	1999-04-21
AU7396398A (en)	1999-01-21
ID20577A (id)	1999-01-14

Legal Events

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

Publication	Publication Date	Title
DE69620364T2 (de)	2002-11-14	Lichtschutzmittel
US5672337A (en)	1997-09-30	Amido photostabilization of dibenzoylmethane sunscreens
AU756928B2 (en)	2003-01-30	Method for improving UV radiation stability of photosensitive sunscreen filters
US5951968A (en)	1999-09-14	UV-photoprotective dibenzoylmethane compositions comprising photostabilizing amounts of benzalmalonate silanes
JP3403625B2 (ja)	2003-05-06	ジベンゾイルメタン誘導体、１，３，５−トリアジン誘導体及びアミド化合物を含む組成物及びその使用
NO312332B1 (no)	2002-04-29	Lysfiltrerende kosmetisk sammensetning og anvendelse av denne
RU2125057C1 (ru)	1999-01-20	Триорганосилановые производные бензотриазола, косметическая композиция для защиты кожи и/или волос от уф-излучений и способ защиты кожи и/или волос от ультрафиолетового излучения
KR100233704B1 (ko)	1999-12-01	차단제의 상승성 혼합물 기재의 피부 및/또는 모발의 광보호용 화장조성물 및 이의 용도
JP3403624B2 (ja)	2003-05-06	ジベンゾイルメタン誘導体、１，３，５−トリアジン誘導体及びベンザルマロナート基を含むケイ素誘導体を含む組成物及びその使用
US5882634A (en)	1999-03-16	Compositions comprising a dibenzoylmethane derivative, a 1,3,5-triazine derivative and a dialkyl benzalmalonate, and methods of use therefor
NO312992B1 (no)	2002-07-29	Anvendelse av <alfa>1<alfa>-dicyano-<beta>1<beta>- difenyletylenforbindelser til fotostabilisering av dibenzoylmetantype UV-A beskyttelsesmidler
AU2005288930B2 (en)	2011-06-23	Photo-stable cosmetic or dermatological compositions
US6071502A (en)	2000-06-06	Photostable sunscreen compositions comprising dibenzoylmethane compounds and 2-hydroxybenzophenone-substituted silanes/organosiloxanes
US6200552B1 (en)	2001-03-13	Photostabilized sunscreen compositions comprising dibenzoylmethane compounds
JP4339136B2 (ja)	2009-10-07	皮膚外用剤
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