DE102004029239A1 - Benyliden-β-dicarbonylverbindungen als neue UV-Absorber - Google Patents
Benyliden-β-dicarbonylverbindungen als neue UV-Absorber Download PDFInfo
- Publication number
- DE102004029239A1 DE102004029239A1 DE102004029239A DE102004029239A DE102004029239A1 DE 102004029239 A1 DE102004029239 A1 DE 102004029239A1 DE 102004029239 A DE102004029239 A DE 102004029239A DE 102004029239 A DE102004029239 A DE 102004029239A DE 102004029239 A1 DE102004029239 A1 DE 102004029239A1
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- Prior art keywords
- alkyl
- cosmetic
- butyl
- phenyl
- acid
- 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.)
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- 239000006096 absorbing agent Substances 0.000 title claims description 36
- 239000000203 mixture Substances 0.000 claims abstract description 108
- 238000009472 formulation Methods 0.000 claims abstract description 73
- 150000001875 compounds Chemical class 0.000 claims abstract description 64
- 239000002537 cosmetic Substances 0.000 claims abstract description 58
- 239000004904 UV filter Substances 0.000 claims abstract description 37
- YBGZDTIWKVFICR-JLHYYAGUSA-N Octyl 4-methoxycinnamic acid Chemical compound CCCCC(CC)COC(=O)\C=C\C1=CC=C(OC)C=C1 YBGZDTIWKVFICR-JLHYYAGUSA-N 0.000 claims abstract description 36
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 20
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 15
- 239000001257 hydrogen Substances 0.000 claims abstract description 14
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims abstract description 13
- NZZIMKJIVMHWJC-UHFFFAOYSA-N dibenzoylmethane Chemical compound C=1C=CC=CC=1C(=O)CC(=O)C1=CC=CC=C1 NZZIMKJIVMHWJC-UHFFFAOYSA-N 0.000 claims abstract description 9
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims abstract description 6
- 125000003118 aryl group Chemical group 0.000 claims abstract description 5
- 125000003545 alkoxy group Chemical group 0.000 claims abstract 4
- -1 n -propyl Chemical group 0.000 claims description 45
- 239000000049 pigment Substances 0.000 claims description 19
- 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
- 230000037072 sun protection Effects 0.000 claims description 8
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims description 7
- 125000001424 substituent group Chemical group 0.000 claims description 7
- 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 claims description 6
- 229910052799 carbon Inorganic materials 0.000 claims description 6
- 229910044991 metal oxide Inorganic materials 0.000 claims description 6
- 150000004706 metal oxides Chemical class 0.000 claims description 5
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 claims description 4
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 4
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 4
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims description 4
- 125000001972 isopentyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])C([H])([H])* 0.000 claims description 2
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims 3
- UUEVFMOUBSLVJW-UHFFFAOYSA-N oxo-[[1-[2-[2-[2-[4-(oxoazaniumylmethylidene)pyridin-1-yl]ethoxy]ethoxy]ethyl]pyridin-4-ylidene]methyl]azanium;dibromide Chemical group [Br-].[Br-].C1=CC(=C[NH+]=O)C=CN1CCOCCOCCN1C=CC(=C[NH+]=O)C=C1 UUEVFMOUBSLVJW-UHFFFAOYSA-N 0.000 claims 2
- 229960001679 octinoxate Drugs 0.000 abstract description 33
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- 125000004453 alkoxycarbonyl group Chemical group 0.000 abstract 1
- 230000010534 mechanism of action Effects 0.000 abstract 1
- FMRHJJZUHUTGKE-UHFFFAOYSA-N Ethylhexyl salicylate Chemical compound CCCCC(CC)COC(=O)C1=CC=CC=C1O FMRHJJZUHUTGKE-UHFFFAOYSA-N 0.000 description 57
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- HEAHZSUCFKFERC-IWGRKNQJSA-N [(2e)-2-[[4-[(e)-[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 group 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-IWGRKNQJSA-N 0.000 description 11
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- 239000004808 2-ethylhexylester Substances 0.000 description 9
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- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 9
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- QMIBDVOQOZDSEN-UHFFFAOYSA-N 2-phenylbenzimidazole-2-sulfonic acid Chemical compound N1=C2C=CC=CC2=NC1(S(=O)(=O)O)C1=CC=CC=C1 QMIBDVOQOZDSEN-UHFFFAOYSA-N 0.000 description 6
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- FDATWRLUYRHCJE-UHFFFAOYSA-N diethylamino hydroxybenzoyl hexyl benzoate Chemical compound CCCCCCOC(=O)C1=CC=CC=C1C(=O)C1=CC=C(N(CC)CC)C=C1O FDATWRLUYRHCJE-UHFFFAOYSA-N 0.000 description 6
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- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 6
- DXGLGDHPHMLXJC-UHFFFAOYSA-N oxybenzone Chemical compound OC1=CC(OC)=CC=C1C(=O)C1=CC=CC=C1 DXGLGDHPHMLXJC-UHFFFAOYSA-N 0.000 description 6
- 238000002360 preparation method Methods 0.000 description 6
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- 235000014113 dietary fatty acids Nutrition 0.000 description 5
- DLAHAXOYRFRPFQ-UHFFFAOYSA-N dodecyl benzoate Chemical compound CCCCCCCCCCCCOC(=O)C1=CC=CC=C1 DLAHAXOYRFRPFQ-UHFFFAOYSA-N 0.000 description 5
- HUVYTMDMDZRHBN-UHFFFAOYSA-N drometrizole trisiloxane Chemical compound C[Si](C)(C)O[Si](C)(O[Si](C)(C)C)CC(C)CC1=CC(C)=CC(N2N=C3C=CC=CC3=N2)=C1O HUVYTMDMDZRHBN-UHFFFAOYSA-N 0.000 description 5
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- WAYINTBTZWQNSN-UHFFFAOYSA-N 11-methyldodecyl 3,5,5-trimethylhexanoate Chemical compound CC(C)CCCCCCCCCCOC(=O)CC(C)CC(C)(C)C WAYINTBTZWQNSN-UHFFFAOYSA-N 0.000 description 4
- 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 4
- 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 4
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- 150000003573 thiols Chemical class 0.000 description 1
- 229940094937 thioredoxin Drugs 0.000 description 1
- 108060008226 thioredoxin Proteins 0.000 description 1
- 239000010936 titanium Substances 0.000 description 1
- 229910052719 titanium Inorganic materials 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
- 125000002640 tocopherol group Chemical class 0.000 description 1
- 235000019149 tocopherols Nutrition 0.000 description 1
- QURCVMIEKCOAJU-UHFFFAOYSA-N trans-isoferulic acid Natural products COC1=CC=C(C=CC(O)=O)C=C1O QURCVMIEKCOAJU-UHFFFAOYSA-N 0.000 description 1
- ZCIHMQAPACOQHT-ZGMPDRQDSA-N trans-isorenieratene Natural products CC(=C/C=C/C=C(C)/C=C/C=C(C)/C=C/c1c(C)ccc(C)c1C)C=CC=C(/C)C=Cc2c(C)ccc(C)c2C ZCIHMQAPACOQHT-ZGMPDRQDSA-N 0.000 description 1
- 150000003626 triacylglycerols Chemical class 0.000 description 1
- 150000003918 triazines Chemical class 0.000 description 1
- 239000001069 triethyl citrate Substances 0.000 description 1
- VMYFZRTXGLUXMZ-UHFFFAOYSA-N triethyl citrate Natural products CCOC(=O)C(O)(C(=O)OCC)C(=O)OCC VMYFZRTXGLUXMZ-UHFFFAOYSA-N 0.000 description 1
- 235000013769 triethyl citrate Nutrition 0.000 description 1
- UFTFJSFQGQCHQW-UHFFFAOYSA-N triformin Chemical compound O=COCC(OC=O)COC=O UFTFJSFQGQCHQW-UHFFFAOYSA-N 0.000 description 1
- OUYCCCASQSFEME-UHFFFAOYSA-N tyrosine Natural products OC(=O)C(N)CC1=CC=C(O)C=C1 OUYCCCASQSFEME-UHFFFAOYSA-N 0.000 description 1
- 229940040064 ubiquinol Drugs 0.000 description 1
- QNTNKSLOFHEFPK-UPTCCGCDSA-N ubiquinol-10 Chemical compound COC1=C(O)C(C)=C(C\C=C(/C)CC\C=C(/C)CC\C=C(/C)CC\C=C(/C)CC\C=C(/C)CC\C=C(/C)CC\C=C(/C)CC\C=C(/C)CC\C=C(/C)CCC=C(C)C)C(O)=C1OC QNTNKSLOFHEFPK-UPTCCGCDSA-N 0.000 description 1
- 229940035936 ubiquinone Drugs 0.000 description 1
- 235000021122 unsaturated fatty acids Nutrition 0.000 description 1
- 150000004670 unsaturated fatty acids Chemical class 0.000 description 1
- 229940116269 uric acid Drugs 0.000 description 1
- 230000000007 visual effect Effects 0.000 description 1
- 235000019154 vitamin C Nutrition 0.000 description 1
- 239000011718 vitamin C Substances 0.000 description 1
- 235000019165 vitamin E Nutrition 0.000 description 1
- 229940046009 vitamin E Drugs 0.000 description 1
- 239000011709 vitamin E Substances 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 239000000230 xanthan gum Substances 0.000 description 1
- 229920001285 xanthan gum Polymers 0.000 description 1
- 229940082509 xanthan gum Drugs 0.000 description 1
- 235000010493 xanthan gum Nutrition 0.000 description 1
- 229910052726 zirconium Inorganic materials 0.000 description 1
- OENHQHLEOONYIE-JLTXGRSLSA-N β-Carotene Chemical compound CC=1CCCC(C)(C)C=1\C=C\C(\C)=C\C=C\C(\C)=C\C=C\C=C(/C)\C=C\C=C(/C)\C=C\C1=C(C)CCCC1(C)C OENHQHLEOONYIE-JLTXGRSLSA-N 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
- A61K8/33—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
- A61K8/37—Esters of carboxylic acids
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C49/00—Ketones; Ketenes; Dimeric ketenes; Ketonic chelates
- C07C49/76—Ketones containing a keto group bound to a six-membered aromatic ring
- C07C49/84—Ketones containing a keto group bound to a six-membered aromatic ring containing ether groups, groups, groups, or groups
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C69/00—Esters of carboxylic acids; Esters of carbonic or haloformic acids
- C07C69/66—Esters of carboxylic acids having esterified carboxylic groups bound to acyclic carbon atoms and having any of the groups OH, O—metal, —CHO, keto, ether, acyloxy, groups, groups, or in the acid moiety
- C07C69/73—Esters of carboxylic acids having esterified carboxylic groups bound to acyclic carbon atoms and having any of the groups OH, O—metal, —CHO, keto, ether, acyloxy, groups, groups, or in the acid moiety of unsaturated acids
- C07C69/738—Esters of keto-carboxylic acids or aldehydo-carboxylic acids
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2601/00—Systems containing only non-condensed rings
- C07C2601/12—Systems containing only non-condensed rings with a six-membered ring
- C07C2601/14—The ring being saturated
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Emergency Medicine (AREA)
- Birds (AREA)
- Epidemiology (AREA)
- Dermatology (AREA)
- Cosmetics (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Priority Applications (16)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE102004029239A DE102004029239A1 (de) | 2004-05-03 | 2004-06-17 | Benyliden-β-dicarbonylverbindungen als neue UV-Absorber |
| PCT/EP2005/051865 WO2005107692A1 (de) | 2004-05-03 | 2005-04-26 | BENZYLIDEN-β-DICARBONYLVERBINDUNGEN ALS NEUE UV-ABSORBER |
| DE502005005550T DE502005005550D1 (de) | 2004-05-03 | 2005-04-26 | BENZYLIDEN-ßDICARBONYLVERBINDUNGEN ALS NEUE UV-ABSORBER |
| JP2007512166A JP2007536332A (ja) | 2004-05-03 | 2005-04-26 | 新規ＵＶ吸収剤としてのベンジリデン−β−ジカルボニル化合物 |
| EP08158316A EP1961453A3 (de) | 2004-05-03 | 2005-04-26 | Benzyliden-ß-dicarbonylverbindungen als UV-Absorber |
| KR1020067022131A KR20070008655A (ko) | 2004-05-03 | 2005-04-26 | 신규한 ＵＶ 흡수제로서의 벤질리덴-β-디카르보닐 화합물 |
| EP05742743A EP1748753B1 (de) | 2004-05-03 | 2005-04-26 | BENZYLIDEN-ßDICARBONYLVERBINDUNGEN ALS NEUE UV-ABSORBER |
| ES05742743T ES2313342T3 (es) | 2004-05-03 | 2005-04-26 | Compuestos de benciliden-b-dicarbolino como nuevos absorbentes uv. |
| CA002563987A CA2563987A1 (en) | 2004-05-03 | 2005-04-26 | Benzylidene-.beta.-dicarbonyl compounds as novel uv-absorbers |
| MXPA06012249A MXPA06012249A (es) | 2004-05-03 | 2005-04-26 | Compuestos de benciliden-beta-dicarbonilo como novedosos absorbentes de luz ultravioleta. |
| US11/568,606 US20080050319A1 (en) | 2004-05-03 | 2005-04-26 | Benzylidene-Alpha-Dicarbonyl Compounds as Novel Uv Absorbers |
| PL05742743T PL1748753T3 (pl) | 2004-05-03 | 2005-04-26 | Związki benzylideno-ß-dikarbonylowe jako nowe absorbery UV |
| AT05742743T ATE409456T1 (de) | 2004-05-03 | 2005-04-26 | Benzyliden-ssdicarbonylverbindungen als neue uv- absorber |
| AU2005239836A AU2005239836A1 (en) | 2004-05-03 | 2005-04-26 | Benzylidene-beta-&bgr;-dicarbonyl compounds as novel UV-absorbers |
| BRPI0510591-9A BRPI0510591A (pt) | 2004-05-03 | 2005-04-26 | compostos benzilideno-beta-dicarbonila como novos filtros de uv |
| IL178362A IL178362A0 (en) | 2004-05-03 | 2006-09-28 | Benzylidene-??-dicarbonyl compounds as novel uv-absorbers |
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE102004021805 | 2004-05-03 | ||
| DE102004021805.6 | 2004-05-03 | ||
| DE102004029239A DE102004029239A1 (de) | 2004-05-03 | 2004-06-17 | Benyliden-β-dicarbonylverbindungen als neue UV-Absorber |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE102004029239A1 true DE102004029239A1 (de) | 2005-12-01 |
Family
ID=34967921
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE102004029239A Withdrawn DE102004029239A1 (de) | 2004-05-03 | 2004-06-17 | Benyliden-β-dicarbonylverbindungen als neue UV-Absorber |
| DE502005005550T Expired - Fee Related DE502005005550D1 (de) | 2004-05-03 | 2005-04-26 | BENZYLIDEN-ßDICARBONYLVERBINDUNGEN ALS NEUE UV-ABSORBER |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE502005005550T Expired - Fee Related DE502005005550D1 (de) | 2004-05-03 | 2005-04-26 | BENZYLIDEN-ßDICARBONYLVERBINDUNGEN ALS NEUE UV-ABSORBER |
Country Status (14)
| Country | Link |
|---|---|
| US (1) | US20080050319A1 (https=) |
| EP (2) | EP1961453A3 (https=) |
| JP (1) | JP2007536332A (https=) |
| KR (1) | KR20070008655A (https=) |
| AT (1) | ATE409456T1 (https=) |
| AU (1) | AU2005239836A1 (https=) |
| BR (1) | BRPI0510591A (https=) |
| CA (1) | CA2563987A1 (https=) |
| DE (2) | DE102004029239A1 (https=) |
| ES (1) | ES2313342T3 (https=) |
| IL (1) | IL178362A0 (https=) |
| MX (1) | MXPA06012249A (https=) |
| PL (1) | PL1748753T3 (https=) |
| WO (1) | WO2005107692A1 (https=) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE102006025057A1 (de) * | 2006-05-24 | 2007-11-29 | Beiersdorf Ag | Kosmetische Lichtschutzzubereitung mit besonderer Textur |
Families Citing this family (42)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US8440172B2 (en) | 2007-07-09 | 2013-05-14 | Symrise Ag | Stable soluble salts of phenylbenzimidazole sulfonic acid at PHS at or below 7.0 |
| US10463891B2 (en) | 2008-09-30 | 2019-11-05 | Symrise Ag | Extracts of Isochrysis sp. |
| EP2193785B1 (en) | 2008-12-05 | 2018-07-18 | Symrise AG | Extracts of Tetraselmis sp. for cosmetic and therapeutic purposes |
| KR101676375B1 (ko) | 2009-04-09 | 2016-11-15 | 시므라이즈 아게 | 피부 자극-완화제로서 트랜스-텔트-부틸 사이클로헥사놀을 포함하는 조성물 |
| US8623340B2 (en) | 2009-04-28 | 2014-01-07 | Symrise Ag | Omega-cyclohexylalkan-1-oles and use thereof as antimicrobial actives to combat body odor |
| EP2295031B1 (de) | 2009-08-05 | 2018-01-10 | Symrise AG | Verwendung von Pterocarpanen als Anti-Cellulite-Wirkstoffe |
| ES2547309T3 (es) | 2009-10-19 | 2015-10-05 | Symrise Ag | Composiciones que contienen fragancias, que comprenden nonanoato de cetilo y/o nonanoato de estearilo |
| EP2184339B1 (de) | 2009-10-19 | 2011-12-14 | Symrise AG | Riechstoffmischungen enthaltend Isolongifolanol und Moschus |
| EP2158896A3 (de) | 2009-11-02 | 2010-09-29 | Symrise GmbH & Co. KG | Riechstoffhaltige Zusammensetzungen umfassend Neopentylglycoldiisononanoat |
| EP2359702B1 (en) | 2010-01-22 | 2014-06-04 | Symrise AG | Solubilization agent for solubilizing polyphenols, flavonoids and/or diterpenoid glucosides |
| BR112012025740B1 (pt) | 2010-04-08 | 2017-12-26 | Symrise Ag | Cosmetic preparation, and use of dihydrodesidrodi-isoeugenol |
| EP2389922A1 (en) | 2010-05-25 | 2011-11-30 | Symrise AG | Cyclohexyl carbamate compounds as anti-ageing actives |
| EP2286908A3 (de) | 2010-11-19 | 2011-06-01 | Symrise AG | Lösungsvermittler für kosmetische Zubereitungen |
| EP2457554A1 (de) | 2010-11-24 | 2012-05-30 | Symrise AG | Menthol enthaltende Mischung |
| EP2356977B1 (de) | 2011-02-02 | 2017-12-27 | Symrise AG | Zubereitungen mit Holzextrakten von Gleditschien |
| EP2524959B1 (de) | 2011-05-17 | 2014-01-22 | Symrise AG | Riech- und/oder Aromastoffkompositionen enthaltend Dioxolane |
| DE102011082464A1 (de) | 2011-09-09 | 2011-12-01 | Symrise Ag | Riechstoffmischungen enthaltend bestimmte Isolongifolenylmethylether |
| WO2013041130A1 (de) | 2011-09-20 | 2013-03-28 | Symrise Ag | Acetale und ketale als riech- und aromastoffe |
| EP2474301B1 (de) | 2011-12-14 | 2014-04-16 | Symrise AG | Riechstoffmischungen enthaltend Cyclopent-2-Enyl-Essigsäureethylester |
| EP2887929A2 (en) | 2012-08-23 | 2015-07-01 | Symrise AG | Compounds for preventing, reducing and/or alleviating itchy skin condition(s) |
| DE102013204097A1 (de) * | 2013-03-11 | 2014-10-30 | Beiersdorf Ag | Wirkstoffkombinationen aus Alkylamidothiazolen und einer oder mehreren kosmetisch oder dermatologisch unbedenklichen UV-Filtersubstanzen |
| JP2015134904A (ja) * | 2013-11-18 | 2015-07-27 | 東洋合成工業株式会社 | 化学種発生向上化合物 |
| ES2819207T3 (es) * | 2014-04-29 | 2021-04-15 | Symrise Ag | Mezclas activas |
| CN109069378B (zh) | 2016-02-15 | 2022-10-11 | 西姆莱斯股份公司 | 含有酯和酮的香料混合物 |
| US11603506B2 (en) | 2016-09-01 | 2023-03-14 | Symrise Ag | Product comprising a plastic container and a substance composition |
| US10920170B2 (en) | 2017-03-21 | 2021-02-16 | Symrise Ag | Fragrance mixtures containing tricyclo[5.2.1.0]-decane-8-ethyl ether |
| WO2018171871A1 (de) | 2017-03-21 | 2018-09-27 | Symrise Ag | 2,3,6-trimethylcyclohexanol als riech- und/oder aromastoff |
| WO2018171865A1 (de) | 2017-03-21 | 2018-09-27 | Symrise Ag | 5-bicyclo[2.2.1]hept-2-enyl-acetat als riech- und/oder aromastoff |
| WO2018192652A1 (de) | 2017-04-19 | 2018-10-25 | Symrise Ag | 1,1-dimeth/ethoxynon-3-in als riechstoff |
| EP3612620B1 (de) | 2017-04-21 | 2021-03-03 | Symrise AG | 4-ethyl-octen-2/3-nitril als riechstoff |
| WO2018196988A1 (de) | 2017-04-28 | 2018-11-01 | Symrise Ag | Ethyl-2-acetyl-2,4-dimethyl-pent-4-enoat als riechstoff |
| EP3723709B1 (de) | 2017-12-14 | 2021-03-31 | Symrise AG | Riechstoffmischungen enthaltend 8,8-dimethyl-6,10-dioxaspiro[4,5]decan |
| WO2018154145A2 (en) | 2018-03-29 | 2018-08-30 | Symrise Ag | Compounds for skin improvement / treatment |
| EP3826986B1 (de) | 2018-07-23 | 2026-03-04 | Symrise AG | Neue riechstoffe mit rosengeruch |
| WO2020233778A1 (de) | 2019-05-17 | 2020-11-26 | Symrise Ag | Duftstoff- oder geschmacksstoffmischung |
| WO2021008696A1 (de) | 2019-07-16 | 2021-01-21 | Symrise Ag | Riechstoffmischung enthaltend 1,3-propandiol |
| CN115427388A (zh) | 2020-04-08 | 2022-12-02 | 西姆莱斯有限公司 | 用作香味化合物的新型酯 |
| EP3944853A1 (en) | 2020-07-31 | 2022-02-02 | Basf Se | Liquid l-menthol composition |
| WO2022128164A1 (en) | 2020-12-14 | 2022-06-23 | Symrise Ag | Extracts of isochrysis species / tisochrysis species |
| US20240130957A1 (en) | 2020-12-14 | 2024-04-25 | Symrise Ag | Extracts of isochrysis species/tisochrysis species |
| CN117651544A (zh) | 2021-07-23 | 2024-03-05 | 西姆莱斯有限公司 | 二咖啡酰奎宁酸及二咖啡酰奎宁酸与生育酚的协同作用 |
| US20240392208A1 (en) | 2021-09-13 | 2024-11-28 | Symrise Ag | Cyclopropanated fragrance compounds |
Family Cites Families (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1087902B (de) | 1956-06-19 | 1960-08-25 | Bayer Ag | Ultraviolett-Schutzfiltermasse oder -schicht |
| DE1914059A1 (de) * | 1969-03-20 | 1970-10-01 | Bayer Ag | UV-Absorber |
| DE3314742C2 (de) | 1983-04-23 | 1987-04-02 | Degussa Ag, 6000 Frankfurt | Verfahren zur Herstellung von an der Oberfläche modifizierten natürlichen, oxidischen oder silikatischen Füllstoffen und deren Verwendung |
| EP0496433B1 (en) | 1987-10-22 | 1999-03-24 | The Procter & Gamble Company | Photoprotection compositions comprising chelating agents |
| GB9110123D0 (en) | 1991-05-10 | 1991-07-03 | Dow Corning | Organosilicon compounds their preparation and use |
| ES2102670T3 (es) | 1992-08-26 | 1997-08-01 | Beiersdorf Ag | Uso de captadores de radicales como agentes inmunomoduladores en composiciones cosmeticas y dermatologicas. |
| EP0911020B1 (de) * | 1997-10-20 | 2004-03-10 | Basf Aktiengesellschaft | Methyl-Styrol derivate als UV-filter und diese enthaltende kosmetische und pharmazeutische Zubereitungen |
| DE19755650A1 (de) | 1997-10-20 | 1999-04-22 | Basf Ag | Photostabile UV-Filter enthaltende kosmetische und pharmazeutische Zubereitungen |
| US5830441A (en) * | 1998-01-20 | 1998-11-03 | Isp Investments Inc. | Photostable UV absorbent containing A-cyano cinnamyl moiety |
| DE19919630A1 (de) | 1999-04-30 | 2000-11-16 | Cognis Deutschland Gmbh | Sonnenschutzmittel |
| DE10055940A1 (de) | 2000-11-10 | 2002-05-29 | Bayer Ag | Neue Indanylidenverbindungen |
-
2004
- 2004-06-17 DE DE102004029239A patent/DE102004029239A1/de not_active Withdrawn
-
2005
- 2005-04-26 DE DE502005005550T patent/DE502005005550D1/de not_active Expired - Fee Related
- 2005-04-26 EP EP08158316A patent/EP1961453A3/de not_active Withdrawn
- 2005-04-26 CA CA002563987A patent/CA2563987A1/en not_active Abandoned
- 2005-04-26 KR KR1020067022131A patent/KR20070008655A/ko not_active Withdrawn
- 2005-04-26 BR BRPI0510591-9A patent/BRPI0510591A/pt not_active IP Right Cessation
- 2005-04-26 AU AU2005239836A patent/AU2005239836A1/en not_active Abandoned
- 2005-04-26 JP JP2007512166A patent/JP2007536332A/ja not_active Abandoned
- 2005-04-26 EP EP05742743A patent/EP1748753B1/de not_active Expired - Lifetime
- 2005-04-26 PL PL05742743T patent/PL1748753T3/pl unknown
- 2005-04-26 MX MXPA06012249A patent/MXPA06012249A/es active IP Right Grant
- 2005-04-26 ES ES05742743T patent/ES2313342T3/es not_active Expired - Lifetime
- 2005-04-26 US US11/568,606 patent/US20080050319A1/en not_active Abandoned
- 2005-04-26 AT AT05742743T patent/ATE409456T1/de not_active IP Right Cessation
- 2005-04-26 WO PCT/EP2005/051865 patent/WO2005107692A1/de not_active Ceased
-
2006
- 2006-09-28 IL IL178362A patent/IL178362A0/en unknown
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE102006025057A1 (de) * | 2006-05-24 | 2007-11-29 | Beiersdorf Ag | Kosmetische Lichtschutzzubereitung mit besonderer Textur |
Also Published As
| Publication number | Publication date |
|---|---|
| KR20070008655A (ko) | 2007-01-17 |
| EP1748753B1 (de) | 2008-10-01 |
| ATE409456T1 (de) | 2008-10-15 |
| IL178362A0 (en) | 2007-07-04 |
| EP1961453A3 (de) | 2009-08-19 |
| EP1961453A2 (de) | 2008-08-27 |
| AU2005239836A1 (en) | 2005-11-17 |
| DE502005005550D1 (de) | 2008-11-13 |
| MXPA06012249A (es) | 2007-01-31 |
| JP2007536332A (ja) | 2007-12-13 |
| CA2563987A1 (en) | 2005-11-17 |
| BRPI0510591A (pt) | 2007-11-20 |
| WO2005107692A8 (de) | 2006-03-16 |
| PL1748753T3 (pl) | 2008-12-31 |
| ES2313342T3 (es) | 2009-03-01 |
| EP1748753A1 (de) | 2007-02-07 |
| WO2005107692A1 (de) | 2005-11-17 |
| US20080050319A1 (en) | 2008-02-28 |
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