ES2354923T3 - Nitrilos alfa, beta-insaturados utilizados como fragancias. - Google Patents
Nitrilos alfa, beta-insaturados utilizados como fragancias. Download PDFInfo
- Publication number
- ES2354923T3 ES2354923T3 ES07800663T ES07800663T ES2354923T3 ES 2354923 T3 ES2354923 T3 ES 2354923T3 ES 07800663 T ES07800663 T ES 07800663T ES 07800663 T ES07800663 T ES 07800663T ES 2354923 T3 ES2354923 T3 ES 2354923T3
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- Prior art keywords
- mixture
- methyl
- fragrance
- compound
- formula
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- 239000003205 fragrance Substances 0.000 title claims abstract description 29
- 239000004615 ingredient Substances 0.000 claims abstract description 10
- 239000000796 flavoring agent Substances 0.000 claims abstract description 6
- 235000019634 flavors Nutrition 0.000 claims abstract description 6
- 239000000203 mixture Substances 0.000 claims description 30
- 150000001875 compounds Chemical class 0.000 claims description 27
- -1 1-methyl-1-propyl Chemical group 0.000 claims description 7
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- 125000006645 (C3-C4) cycloalkyl group Chemical group 0.000 claims description 5
- 125000000217 alkyl group Chemical group 0.000 claims description 5
- 239000000463 material Substances 0.000 claims description 5
- 239000002304 perfume Substances 0.000 claims description 5
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- RIMSHACPVDNYFC-UHFFFAOYSA-N 4-methylhex-2-enenitrile Chemical compound CCC(C)C=CC#N RIMSHACPVDNYFC-UHFFFAOYSA-N 0.000 claims description 3
- 239000002537 cosmetic Substances 0.000 claims description 3
- JAIOXBDVPQJCCD-UHFFFAOYSA-N hept-2-enenitrile Chemical compound CCCCC=CC#N JAIOXBDVPQJCCD-UHFFFAOYSA-N 0.000 claims description 3
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- 230000002708 enhancing effect Effects 0.000 claims 1
- 150000002825 nitriles Chemical class 0.000 abstract description 3
- HEDRZPFGACZZDS-MICDWDOJSA-N Trichloro(2H)methane Chemical compound [2H]C(Cl)(Cl)Cl HEDRZPFGACZZDS-MICDWDOJSA-N 0.000 description 40
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- 239000001939 cymbopogon martini roxb. stapf. oil Substances 0.000 description 1
- SQIFACVGCPWBQZ-UHFFFAOYSA-N delta-terpineol Natural products CC(C)(O)C1CCC(=C)CC1 SQIFACVGCPWBQZ-UHFFFAOYSA-N 0.000 description 1
- 239000002781 deodorant agent Substances 0.000 description 1
- 238000004851 dishwashing Methods 0.000 description 1
- 235000013399 edible fruits Nutrition 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 239000001813 ethyl (2R)-2-methylbutanoate Substances 0.000 description 1
- GUAPMIRFNRZYFI-UHFFFAOYSA-N ethyl 2,3,6,6-tetramethylcyclohex-2-ene-1-carboxylate Chemical compound CCOC(=O)C1C(C)=C(C)CCC1(C)C GUAPMIRFNRZYFI-UHFFFAOYSA-N 0.000 description 1
- CQHUPYQUERYPML-UHFFFAOYSA-N ethyl 2-ethyl-6,6-dimethylcyclohex-2-ene-1-carboxylate Chemical compound CCOC(=O)C1C(CC)=CCCC1(C)C CQHUPYQUERYPML-UHFFFAOYSA-N 0.000 description 1
- 229940090910 ethyl 2-methylbutyrate Drugs 0.000 description 1
- 229960002217 eugenol Drugs 0.000 description 1
- 239000000284 extract Substances 0.000 description 1
- 239000002979 fabric softener Substances 0.000 description 1
- 229940043259 farnesol Drugs 0.000 description 1
- 229930002886 farnesol Natural products 0.000 description 1
- 239000010408 film Substances 0.000 description 1
- IFYYFLINQYPWGJ-VIFPVBQESA-N gamma-Decalactone Natural products CCCCCC[C@H]1CCC(=O)O1 IFYYFLINQYPWGJ-VIFPVBQESA-N 0.000 description 1
- PHXATPHONSXBIL-JTQLQIEISA-N gamma-Undecalactone Natural products CCCCCCC[C@H]1CCC(=O)O1 PHXATPHONSXBIL-JTQLQIEISA-N 0.000 description 1
- 229940020436 gamma-undecalactone Drugs 0.000 description 1
- HIGQPQRQIQDZMP-UHFFFAOYSA-N geranil acetate Natural products CC(C)=CCCC(C)=CCOC(C)=O HIGQPQRQIQDZMP-UHFFFAOYSA-N 0.000 description 1
- HIGQPQRQIQDZMP-DHZHZOJOSA-N geranyl acetate Chemical compound CC(C)=CCC\C(C)=C\COC(C)=O HIGQPQRQIQDZMP-DHZHZOJOSA-N 0.000 description 1
- 125000000623 heterocyclic group Chemical group 0.000 description 1
- UFLHIIWVXFIJGU-UHFFFAOYSA-N hex-3-en-1-ol Natural products CCC=CCCO UFLHIIWVXFIJGU-UHFFFAOYSA-N 0.000 description 1
- 229930002839 ionone Natural products 0.000 description 1
- 150000002499 ionone derivatives Chemical class 0.000 description 1
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 239000010656 jasmine oil Substances 0.000 description 1
- 239000000171 lavandula angustifolia l. flower oil Substances 0.000 description 1
- SDQFDHOLCGWZPU-UHFFFAOYSA-N lilial Chemical compound O=CC(C)CC1=CC=C(C(C)(C)C)C=C1 SDQFDHOLCGWZPU-UHFFFAOYSA-N 0.000 description 1
- 239000002502 liposome Substances 0.000 description 1
- 150000002678 macrocyclic compounds Chemical class 0.000 description 1
- 229940043353 maltol Drugs 0.000 description 1
- 229940041616 menthol Drugs 0.000 description 1
- KVWWIYGFBYDJQC-UHFFFAOYSA-N methyl dihydrojasmonate Chemical compound CCCCCC1C(CC(=O)OC)CCC1=O KVWWIYGFBYDJQC-UHFFFAOYSA-N 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 239000003094 microcapsule Substances 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 235000010460 mustard Nutrition 0.000 description 1
- MEJYWDUBOCZFFS-UHFFFAOYSA-N n-(2,4,4,7-tetramethylnona-6,8-dien-3-ylidene)hydroxylamine Chemical compound CC(C)C(=NO)C(C)(C)CC=C(C)C=C MEJYWDUBOCZFFS-UHFFFAOYSA-N 0.000 description 1
- 239000002088 nanocapsule Substances 0.000 description 1
- 229930014626 natural product Natural products 0.000 description 1
- 229920001542 oligosaccharide Polymers 0.000 description 1
- 239000012188 paraffin wax Substances 0.000 description 1
- 239000000546 pharmaceutical excipient Substances 0.000 description 1
- 229940067107 phenylethyl alcohol Drugs 0.000 description 1
- 239000001738 pogostemon cablin oil Substances 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 238000002953 preparative HPLC Methods 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 235000019719 rose oil Nutrition 0.000 description 1
- 239000010666 rose oil Substances 0.000 description 1
- 229930007790 rose oxide Natural products 0.000 description 1
- 239000010671 sandalwood oil Substances 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 239000002453 shampoo Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 230000000707 stereoselective effect Effects 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- KDYFGRWQOYBRFD-UHFFFAOYSA-N succinic acid Chemical compound OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 229940116411 terpineol Drugs 0.000 description 1
- LFSYLMRHJKGLDV-UHFFFAOYSA-N tetradecanolide Natural products O=C1CCCCCCCCCCCCCO1 LFSYLMRHJKGLDV-UHFFFAOYSA-N 0.000 description 1
- CRDAMVZIKSXKFV-UHFFFAOYSA-N trans-Farnesol Natural products CC(C)=CCCC(C)=CCCC(C)=CCO CRDAMVZIKSXKFV-UHFFFAOYSA-N 0.000 description 1
- MWOOGOJBHIARFG-UHFFFAOYSA-N vanillin Chemical compound COC1=CC(C=O)=CC=C1O MWOOGOJBHIARFG-UHFFFAOYSA-N 0.000 description 1
- FGQOOHJZONJGDT-UHFFFAOYSA-N vanillin Natural products COC1=CC(O)=CC(C=O)=C1 FGQOOHJZONJGDT-UHFFFAOYSA-N 0.000 description 1
- 235000012141 vanillin Nutrition 0.000 description 1
- DCSCXTJOXBUFGB-UHFFFAOYSA-N verbenone Natural products CC1=CC(=O)C2C(C)(C)C1C2 DCSCXTJOXBUFGB-UHFFFAOYSA-N 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 239000010457 zeolite Substances 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
- C11B9/0007—Aliphatic compounds
- C11B9/0023—Aliphatic compounds containing nitrogen as the only heteroatom
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23L—FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES, NOT OTHERWISE PROVIDED FOR; PREPARATION OR TREATMENT THEREOF
- A23L27/00—Spices; Flavouring agents or condiments; Artificial sweetening agents; Table salts; Dietetic salt substitutes; Preparation or treatment thereof
- A23L27/20—Synthetic spices, flavouring agents or condiments
- A23L27/202—Aliphatic compounds
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23L—FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES, NOT OTHERWISE PROVIDED FOR; PREPARATION OR TREATMENT THEREOF
- A23L27/00—Spices; Flavouring agents or condiments; Artificial sweetening agents; Table salts; Dietetic salt substitutes; Preparation or treatment thereof
- A23L27/20—Synthetic spices, flavouring agents or condiments
- A23L27/203—Alicyclic compounds
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C255/00—Carboxylic acid nitriles
- C07C255/01—Carboxylic acid nitriles having cyano groups bound to acyclic carbon atoms
- C07C255/06—Carboxylic acid nitriles having cyano groups bound to acyclic carbon atoms of an acyclic and unsaturated carbon skeleton
- C07C255/07—Mononitriles
-
- 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
- C11B9/0026—Essential oils; Perfumes compounds containing an alicyclic ring not condensed with another ring
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Life Sciences & Earth Sciences (AREA)
- Nutrition Science (AREA)
- Wood Science & Technology (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Food Science & Technology (AREA)
- Polymers & Plastics (AREA)
- Fats And Perfumes (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Cosmetics (AREA)
- Detergent Compositions (AREA)
- Medicines Containing Material From Animals Or Micro-Organisms (AREA)
- Dental Preparations (AREA)
- Seasonings (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB0618870 | 2006-09-26 | ||
| GBGB0618870.0A GB0618870D0 (en) | 2006-09-26 | 2006-09-26 | Organic compounds |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ES2354923T3 true ES2354923T3 (es) | 2011-03-21 |
Family
ID=37421586
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES07800663T Active ES2354923T3 (es) | 2006-09-26 | 2007-09-26 | Nitrilos alfa, beta-insaturados utilizados como fragancias. |
Country Status (11)
| Country | Link |
|---|---|
| US (1) | US20110207835A1 (enExample) |
| EP (1) | EP2079436B1 (enExample) |
| JP (1) | JP2010504415A (enExample) |
| CN (1) | CN101516324A (enExample) |
| AT (1) | ATE487464T1 (enExample) |
| BR (1) | BRPI0717083A2 (enExample) |
| DE (1) | DE602007010502D1 (enExample) |
| ES (1) | ES2354923T3 (enExample) |
| GB (1) | GB0618870D0 (enExample) |
| MX (1) | MX2009002539A (enExample) |
| WO (1) | WO2008037105A1 (enExample) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP3612620B1 (de) * | 2017-04-21 | 2021-03-03 | Symrise AG | 4-ethyl-octen-2/3-nitril als riechstoff |
Family Cites Families (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5835180B2 (ja) * | 1975-08-21 | 1983-08-01 | ロ−ヌ.プ−ラン.Ind | α、β不飽和ニトリルの製造法 |
| GB1593181A (en) * | 1977-03-23 | 1981-07-15 | Polak Frutal Works | Carane derivatives and their use in fragrance materials |
| CA1118450A (en) * | 1978-03-20 | 1982-02-16 | Willem Lenselink | Menthane nitriles |
| US4277377A (en) * | 1979-03-22 | 1981-07-07 | Bush Boake Allen Limited | Perfume compositions containing dimethyl heptenonitriles |
| US4451479A (en) * | 1981-07-13 | 1984-05-29 | American Cyanamid Company | Therapeutically active 3-amino-1-halogenated phenyl-2-pyrazolines and their C4 and C5 analogs |
| DE3914391A1 (de) * | 1989-04-29 | 1991-01-17 | Basf Ag | Ss,(gamma)-ungesaettigte nitrile, deren herstellung und verwendung als riechstoffe |
| DE3932325A1 (de) * | 1989-09-28 | 1991-04-11 | Haarmann & Reimer Gmbh | Alkadiennitrile, verfahren zu ihrer herstellung und ihre verwendung |
| JPH11501614A (ja) * | 1994-12-15 | 1999-02-09 | クエスト・インターナショナル・ビー・ブイ | シクロヘキシルプロピオニトリル及びシクロヘキセニルプロピオニトリル |
| US6114565A (en) * | 1999-09-03 | 2000-09-05 | Millennium Specialty Chemicals | Process for obtaining nitriles |
| DE10022076A1 (de) * | 2000-05-06 | 2001-11-08 | Cognis Deutschland Gmbh | Trimethyldecen-Verbindungen |
| MX2007006583A (es) * | 2004-12-08 | 2007-06-15 | Givaudan Sa | Compuestos organicos. |
| GB0428306D0 (en) * | 2004-12-24 | 2005-01-26 | Givaudan Sa | Compound |
-
2006
- 2006-09-26 GB GBGB0618870.0A patent/GB0618870D0/en not_active Ceased
-
2007
- 2007-09-26 MX MX2009002539A patent/MX2009002539A/es active IP Right Grant
- 2007-09-26 US US12/441,786 patent/US20110207835A1/en not_active Abandoned
- 2007-09-26 ES ES07800663T patent/ES2354923T3/es active Active
- 2007-09-26 CN CNA2007800357869A patent/CN101516324A/zh active Pending
- 2007-09-26 WO PCT/CH2007/000472 patent/WO2008037105A1/en not_active Ceased
- 2007-09-26 BR BRPI0717083-1A2A patent/BRPI0717083A2/pt not_active IP Right Cessation
- 2007-09-26 EP EP07800663A patent/EP2079436B1/en not_active Not-in-force
- 2007-09-26 DE DE602007010502T patent/DE602007010502D1/de active Active
- 2007-09-26 JP JP2009529485A patent/JP2010504415A/ja not_active Ceased
- 2007-09-26 AT AT07800663T patent/ATE487464T1/de not_active IP Right Cessation
Also Published As
| Publication number | Publication date |
|---|---|
| CN101516324A (zh) | 2009-08-26 |
| EP2079436A1 (en) | 2009-07-22 |
| DE602007010502D1 (enExample) | 2010-12-23 |
| BRPI0717083A2 (pt) | 2013-10-29 |
| EP2079436B1 (en) | 2010-11-10 |
| GB0618870D0 (en) | 2006-11-01 |
| JP2010504415A (ja) | 2010-02-12 |
| US20110207835A1 (en) | 2011-08-25 |
| ATE487464T1 (de) | 2010-11-15 |
| WO2008037105A1 (en) | 2008-04-03 |
| MX2009002539A (es) | 2009-03-20 |
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