ES2671641T3 - Nuevas mezclas con (4aR,5R,7aS,9R)-octahidro-2,2,5,8,8,9a-hexametil-4H-4a,9-metanoazuleno(5,6-d)-1,3-dioxol) (Ambrocenide®) - Google Patents
Nuevas mezclas con (4aR,5R,7aS,9R)-octahidro-2,2,5,8,8,9a-hexametil-4H-4a,9-metanoazuleno(5,6-d)-1,3-dioxol) (Ambrocenide®) Download PDFInfo
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- ES2671641T3 ES2671641T3 ES14169354.9T ES14169354T ES2671641T3 ES 2671641 T3 ES2671641 T3 ES 2671641T3 ES 14169354 T ES14169354 T ES 14169354T ES 2671641 T3 ES2671641 T3 ES 2671641T3
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- 238000007171 acid catalysis Methods 0.000 description 1
- 239000000443 aerosol Substances 0.000 description 1
- GUUHFMWKWLOQMM-NTCAYCPXSA-N alpha-hexylcinnamaldehyde Chemical compound CCCCCC\C(C=O)=C/C1=CC=CC=C1 GUUHFMWKWLOQMM-NTCAYCPXSA-N 0.000 description 1
- GUUHFMWKWLOQMM-UHFFFAOYSA-N alpha-n-hexylcinnamic aldehyde Natural products CCCCCCC(C=O)=CC1=CC=CC=C1 GUUHFMWKWLOQMM-UHFFFAOYSA-N 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- ISAOCJYIOMOJEB-UHFFFAOYSA-N benzoin Chemical compound C=1C=CC=CC=1C(O)C(=O)C1=CC=CC=C1 ISAOCJYIOMOJEB-UHFFFAOYSA-N 0.000 description 1
- 229940007550 benzyl acetate Drugs 0.000 description 1
- POIARNZEYGURDG-FNORWQNLSA-N beta-damascenone Chemical compound C\C=C\C(=O)C1=C(C)C=CCC1(C)C POIARNZEYGURDG-FNORWQNLSA-N 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- FUSUHKVFWTUUBE-UHFFFAOYSA-N buten-2-one Chemical compound CC(=O)C=C FUSUHKVFWTUUBE-UHFFFAOYSA-N 0.000 description 1
- 239000010627 cedar oil Substances 0.000 description 1
- NPFVOOAXDOBMCE-PLNGDYQASA-N cis-3-Hexenyl acetate Natural products CC\C=C/CCOC(C)=O NPFVOOAXDOBMCE-PLNGDYQASA-N 0.000 description 1
- RRGOKSYVAZDNKR-ARJAWSKDSA-M cis-3-hexenylacetate Chemical compound CC\C=C/CCCC([O-])=O RRGOKSYVAZDNKR-ARJAWSKDSA-M 0.000 description 1
- 239000001926 citrus aurantium l. subsp. bergamia wright et arn. oil Substances 0.000 description 1
- 230000003749 cleanliness Effects 0.000 description 1
- 229960000956 coumarin Drugs 0.000 description 1
- 235000001671 coumarin Nutrition 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- HFJRKMMYBMWEAD-UHFFFAOYSA-N dodecanal Chemical compound CCCCCCCCCCCC=O HFJRKMMYBMWEAD-UHFFFAOYSA-N 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000001148 ferula galbaniflua oil terpeneless Substances 0.000 description 1
- 238000004817 gas chromatography Methods 0.000 description 1
- 230000004313 glare Effects 0.000 description 1
- 239000003722 gum benzoin Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- IUSBVFZKQJGVEP-SNAWJCMRSA-N isoeugenol acetate Chemical compound COC1=CC(\C=C\C)=CC=C1OC(C)=O IUSBVFZKQJGVEP-SNAWJCMRSA-N 0.000 description 1
- NBCMACYORPIYNY-UHFFFAOYSA-N jasmolactone Chemical compound CC=CCCC1CCCC(=O)O1 NBCMACYORPIYNY-UHFFFAOYSA-N 0.000 description 1
- 150000002596 lactones Chemical class 0.000 description 1
- TUVXRDNMAFEUBI-UHFFFAOYSA-N lactoscatone Chemical compound C1CC2(C)CC3C(C)(C)CCCC31OC2=O TUVXRDNMAFEUBI-UHFFFAOYSA-N 0.000 description 1
- 239000000171 lavandula angustifolia l. flower oil Substances 0.000 description 1
- 230000003902 lesion Effects 0.000 description 1
- HADJSPUPIRDMDH-UHFFFAOYSA-N methyl acetate;2-pentylcyclopentan-1-one Chemical compound COC(C)=O.CCCCCC1CCCC1=O HADJSPUPIRDMDH-UHFFFAOYSA-N 0.000 description 1
- HRGPYCVTDOECMG-RHBQXOTJSA-N methyl cedryl ether Chemical compound C1[C@@]23[C@H](C)CC[C@H]2C(C)(C)[C@]1([H])[C@@](OC)(C)CC3 HRGPYCVTDOECMG-RHBQXOTJSA-N 0.000 description 1
- KVWWIYGFBYDJQC-UHFFFAOYSA-N methyl dihydrojasmonate Chemical compound CCCCCC1C(CC(=O)OC)CCC1=O KVWWIYGFBYDJQC-UHFFFAOYSA-N 0.000 description 1
- 235000019198 oils Nutrition 0.000 description 1
- 239000010502 orange oil Substances 0.000 description 1
- 229940067107 phenylethyl alcohol Drugs 0.000 description 1
- 239000001738 pogostemon cablin oil Substances 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 238000007142 ring opening reaction Methods 0.000 description 1
- 239000002453 shampoo Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 150000003505 terpenes Chemical class 0.000 description 1
- 235000007586 terpenes Nutrition 0.000 description 1
- UHUFTBALEZWWIH-UHFFFAOYSA-N tetradecanal Chemical compound CCCCCCCCCCCCCC=O UHUFTBALEZWWIH-UHFFFAOYSA-N 0.000 description 1
- 239000010678 thyme oil Substances 0.000 description 1
- NPFVOOAXDOBMCE-UHFFFAOYSA-N trans-3-hexenyl acetate Natural products CCC=CCCOC(C)=O NPFVOOAXDOBMCE-UHFFFAOYSA-N 0.000 description 1
- 229930007850 β-damascenone Natural products 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11B—PRODUCING, e.g. BY PRESSING RAW MATERIALS OR BY EXTRACTION FROM WASTE MATERIALS, REFINING OR PRESERVING FATS, FATTY SUBSTANCES, e.g. LANOLIN, FATTY OILS OR WAXES; ESSENTIAL OILS; PERFUMES
- C11B9/00—Essential oils; Perfumes
- C11B9/0069—Heterocyclic compounds
- C11B9/0073—Heterocyclic compounds containing only O or S as heteroatoms
- C11B9/0076—Heterocyclic compounds containing only O or S as heteroatoms the hetero rings containing less than six atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D317/00—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms
- C07D317/08—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3
- C07D317/44—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3 ortho- or peri-condensed with carbocyclic rings or ring systems
- C07D317/70—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3 ortho- or peri-condensed with carbocyclic rings or ring systems condensed with ring systems containing two or more relevant rings
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Wood Science & Technology (AREA)
- Fats And Perfumes (AREA)
- Cosmetics (AREA)
- Detergent Compositions (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Manufacture Of Tobacco Products (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP14169354.9A EP2947078B1 (de) | 2014-05-21 | 2014-05-21 | Neue Mischungen mit (4aR,5R,7aS,9R)-Octahydro-2,2,5,8,8,9a-hexamethyl-4H-4a,9-Methanoazuleno(5,6-d)-1,3-dioxol) (Ambrocenide®) |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ES2671641T3 true ES2671641T3 (es) | 2018-06-07 |
Family
ID=50732983
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES14169354.9T Active ES2671641T3 (es) | 2014-05-21 | 2014-05-21 | Nuevas mezclas con (4aR,5R,7aS,9R)-octahidro-2,2,5,8,8,9a-hexametil-4H-4a,9-metanoazuleno(5,6-d)-1,3-dioxol) (Ambrocenide®) |
Country Status (9)
| Country | Link |
|---|---|
| US (1) | US10526563B2 (https=) |
| EP (1) | EP2947078B1 (https=) |
| JP (1) | JP6564399B2 (https=) |
| CN (1) | CN106458959B (https=) |
| BR (1) | BR112016027144B1 (https=) |
| ES (1) | ES2671641T3 (https=) |
| MX (1) | MX362230B (https=) |
| TR (1) | TR201808510T4 (https=) |
| WO (1) | WO2015176833A1 (https=) |
Families Citing this family (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB201521861D0 (en) | 2015-12-11 | 2016-01-27 | Givaudan Sa | Improvements in or relating to organic compounds |
| CN111108100B (zh) * | 2017-08-09 | 2023-08-01 | 西姆莱斯有限公司 | 帝王龙涎用于增强铃兰调的用途 |
| DE202017007101U1 (de) | 2017-08-25 | 2019-07-10 | Symrise Ag | Mischungen enthaltend enantiomerenreines Ambrocenide® |
| WO2017186973A2 (de) | 2017-08-25 | 2017-11-02 | Symrise Ag | Mischungen enthaltend enantiomerenreines ambrocenide® |
| ES2887600T3 (es) * | 2017-11-28 | 2021-12-23 | Firmenich & Cie | Ambar odorante |
| SG11202108961WA (en) * | 2019-03-13 | 2021-09-29 | Givaudan Sa | (3aS,4aR,5S,7aS,9R,9aR)-2,2,5,8,8,9a-hexamethyloctahydro-4H-4a,9-methanoazuleno[5,6-d][1,3]dioxole |
| EP3997234A1 (en) * | 2019-07-08 | 2022-05-18 | Symrise AG | Biotechnological production of diols |
| WO2025233712A1 (en) | 2024-05-09 | 2025-11-13 | Politecnico Di Milano | Synthesis method of cedrene cis-diol |
Family Cites Families (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE19704484A1 (de) * | 1997-02-06 | 1998-09-03 | Dragoco Gerberding Co Ag | Cyclische Cedren-Acetale, ihre Herstellung und ihre Verwendung |
| CN1142156C (zh) * | 1998-08-07 | 2004-03-17 | 希姆莱塞两合公司 | 环雪松烯缩醛、其制备和其应用 |
| US7419943B2 (en) * | 2004-08-20 | 2008-09-02 | International Flavors & Fragrances Inc. | Methanoazuenofurans and methanoazulenone compounds and uses of these compounds as fragrance materials |
| ATE496111T1 (de) * | 2007-01-02 | 2011-02-15 | Symrise Ag | Mischungen von 3-(4-methyl-cyclohex-3-enyl)- butyraldehyd und ambro-cenide sowie deren verwendungen und verfahren |
| EP2287158B1 (de) * | 2010-09-29 | 2012-11-14 | Symrise AG | Ambra-Riechstoff auf Basis von 9-Methanoazuleno(5,6-d)-1,3-dioxolen |
| CN102134228B (zh) * | 2011-01-30 | 2012-11-28 | 北京安胜瑞力科技有限公司 | 一种木香-龙涎香型的香料的制备方法 |
| EP2474301B1 (de) * | 2011-12-14 | 2014-04-16 | Symrise AG | Riechstoffmischungen enthaltend Cyclopent-2-Enyl-Essigsäureethylester |
-
2014
- 2014-05-21 TR TR2018/08510T patent/TR201808510T4/tr unknown
- 2014-05-21 ES ES14169354.9T patent/ES2671641T3/es active Active
- 2014-05-21 EP EP14169354.9A patent/EP2947078B1/de active Active
-
2015
- 2015-02-26 WO PCT/EP2015/054027 patent/WO2015176833A1/de not_active Ceased
- 2015-02-26 US US15/312,545 patent/US10526563B2/en active Active
- 2015-02-26 JP JP2016568821A patent/JP6564399B2/ja active Active
- 2015-02-26 BR BR112016027144-0A patent/BR112016027144B1/pt active IP Right Grant
- 2015-02-26 CN CN201580026098.0A patent/CN106458959B/zh active Active
- 2015-02-26 MX MX2016014973A patent/MX362230B/es active IP Right Grant
Also Published As
| Publication number | Publication date |
|---|---|
| US20170114299A1 (en) | 2017-04-27 |
| MX362230B (es) | 2019-01-09 |
| CN106458959A (zh) | 2017-02-22 |
| US10526563B2 (en) | 2020-01-07 |
| CN106458959B (zh) | 2020-03-06 |
| JP6564399B2 (ja) | 2019-08-21 |
| TR201808510T4 (tr) | 2018-07-23 |
| EP2947078B1 (de) | 2018-03-21 |
| BR112016027144B1 (pt) | 2021-02-23 |
| EP2947078A1 (de) | 2015-11-25 |
| WO2015176833A1 (de) | 2015-11-26 |
| MX2016014973A (es) | 2017-03-27 |
| JP2017517509A (ja) | 2017-06-29 |
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