CH617851A5 - Use of 5-oxa-2-methyl-7-phenyl-2-heptene as a fragrance - Google Patents
Use of 5-oxa-2-methyl-7-phenyl-2-heptene as a fragrance Download PDFInfo
- Publication number
- CH617851A5 CH617851A5 CH1541576A CH1541576A CH617851A5 CH 617851 A5 CH617851 A5 CH 617851A5 CH 1541576 A CH1541576 A CH 1541576A CH 1541576 A CH1541576 A CH 1541576A CH 617851 A5 CH617851 A5 CH 617851A5
- Authority
- CH
- Switzerland
- Prior art keywords
- methyl
- heptene
- oxa
- phenyl
- compound
- Prior art date
Links
- WNXBRCWBIGPREJ-UHFFFAOYSA-N 2-(3-methylbut-2-enoxy)ethylbenzene Chemical compound CC(C)=CCOCCC1=CC=CC=C1 WNXBRCWBIGPREJ-UHFFFAOYSA-N 0.000 title claims abstract description 21
- 239000003205 fragrance Substances 0.000 title abstract description 4
- 239000000203 mixture Substances 0.000 claims abstract description 15
- 239000002304 perfume Substances 0.000 claims abstract description 12
- 239000002537 cosmetic Substances 0.000 claims abstract description 10
- 241001104043 Syringa Species 0.000 abstract description 6
- 235000004338 Syringa vulgaris Nutrition 0.000 abstract description 6
- 240000006568 Lathyrus odoratus Species 0.000 abstract description 3
- 150000001875 compounds Chemical class 0.000 description 19
- WRMNZCZEMHIOCP-UHFFFAOYSA-N 2-phenylethanol Chemical compound OCCC1=CC=CC=C1 WRMNZCZEMHIOCP-UHFFFAOYSA-N 0.000 description 10
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 9
- 239000000047 product Substances 0.000 description 9
- 239000000344 soap Substances 0.000 description 6
- 229940067107 phenylethyl alcohol Drugs 0.000 description 5
- QUKGYYKBILRGFE-UHFFFAOYSA-N benzyl acetate Chemical compound CC(=O)OCC1=CC=CC=C1 QUKGYYKBILRGFE-UHFFFAOYSA-N 0.000 description 4
- 239000004615 ingredient Substances 0.000 description 4
- 239000002453 shampoo Substances 0.000 description 4
- OOCCDEMITAIZTP-QPJJXVBHSA-N (E)-cinnamyl alcohol Chemical compound OC\C=C\C1=CC=CC=C1 OOCCDEMITAIZTP-QPJJXVBHSA-N 0.000 description 3
- 240000004713 Pisum sativum Species 0.000 description 3
- 235000010582 Pisum sativum Nutrition 0.000 description 3
- OOCCDEMITAIZTP-UHFFFAOYSA-N allylic benzylic alcohol Natural products OCC=CC1=CC=CC=C1 OOCCDEMITAIZTP-UHFFFAOYSA-N 0.000 description 3
- 230000001166 anti-perspirative effect Effects 0.000 description 3
- 239000003213 antiperspirant Substances 0.000 description 3
- WPFVBOQKRVRMJB-UHFFFAOYSA-N hydroxycitronellal Chemical compound O=CCC(C)CCCC(C)(C)O WPFVBOQKRVRMJB-UHFFFAOYSA-N 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- JKXQKGNGJVZKFA-UHFFFAOYSA-N 1-chloro-3-methylbut-2-ene Chemical compound CC(C)=CCCl JKXQKGNGJVZKFA-UHFFFAOYSA-N 0.000 description 2
- 244000130592 Hibiscus syriacus Species 0.000 description 2
- 235000018081 Hibiscus syriacus Nutrition 0.000 description 2
- SIKJAQJRHWYJAI-UHFFFAOYSA-N Indole Chemical compound C1=CC=C2NC=CC2=C1 SIKJAQJRHWYJAI-UHFFFAOYSA-N 0.000 description 2
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 2
- 239000000443 aerosol Substances 0.000 description 2
- WUOACPNHFRMFPN-UHFFFAOYSA-N alpha-terpineol Chemical compound CC1=CCC(C(C)(C)O)CC1 WUOACPNHFRMFPN-UHFFFAOYSA-N 0.000 description 2
- 229940007550 benzyl acetate Drugs 0.000 description 2
- BJIOGJUNALELMI-ARJAWSKDSA-N cis-isoeugenol Chemical compound COC1=CC(\C=C/C)=CC=C1O BJIOGJUNALELMI-ARJAWSKDSA-N 0.000 description 2
- SQIFACVGCPWBQZ-UHFFFAOYSA-N delta-terpineol Natural products CC(C)(O)C1CCC(=C)CC1 SQIFACVGCPWBQZ-UHFFFAOYSA-N 0.000 description 2
- SZXQTJUDPRGNJN-UHFFFAOYSA-N dipropylene glycol Chemical compound OCCCOCCCO SZXQTJUDPRGNJN-UHFFFAOYSA-N 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 239000012074 organic phase Substances 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 229940116411 terpineol Drugs 0.000 description 2
- PDEQKAVEYSOLJX-RQGDDBKYSA-N (z)-5-[(1r,3r,6s)-2,3-dimethyl-4,5,6,7-tetrahydro-1h-tricyclo[2.2.1.0^{2,6}]heptan-3-yl]-2-methylpent-2-en-1-ol Chemical compound C1[C@@H]2C3(C)[C@@H]2CC1[C@@]3(C)CC/C=C(CO)/C PDEQKAVEYSOLJX-RQGDDBKYSA-N 0.000 description 1
- HPMSQLYFMOOLKS-UHFFFAOYSA-N 1-ethoxy-3-methylbut-2-ene Chemical compound CCOCC=C(C)C HPMSQLYFMOOLKS-UHFFFAOYSA-N 0.000 description 1
- XJWZDXFFNOMMTD-UHFFFAOYSA-N 1-methyl-4-propan-2-ylcyclohex-3-en-1-ol Chemical compound CC(C)C1=CCC(C)(O)CC1 XJWZDXFFNOMMTD-UHFFFAOYSA-N 0.000 description 1
- BHQBQWOZHYUVTL-UHFFFAOYSA-N 2-(3-methylbutoxy)ethylbenzene Chemical compound CC(C)CCOCCC1=CC=CC=C1 BHQBQWOZHYUVTL-UHFFFAOYSA-N 0.000 description 1
- 241000196324 Embryophyta Species 0.000 description 1
- 241000447437 Gerreidae Species 0.000 description 1
- 241000218033 Hibiscus Species 0.000 description 1
- 235000005206 Hibiscus Nutrition 0.000 description 1
- 235000007185 Hibiscus lunariifolius Nutrition 0.000 description 1
- 241001632576 Hyacinthus Species 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 241000220317 Rosa Species 0.000 description 1
- 240000000513 Santalum album Species 0.000 description 1
- 235000008632 Santalum album Nutrition 0.000 description 1
- KEAYESYHFKHZAL-UHFFFAOYSA-N Sodium Chemical compound [Na] KEAYESYHFKHZAL-UHFFFAOYSA-N 0.000 description 1
- GPHUMLIWFXPRJD-UHFFFAOYSA-N [5-methyl-3-(5-methyl-1-phenylhex-4-en-3-yl)oxyhex-4-enyl]benzene Chemical compound C1(=CC=CC=C1)CCC(C=C(C)C)OC(C=C(C)C)CCC1=CC=CC=C1 GPHUMLIWFXPRJD-UHFFFAOYSA-N 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
- 239000008346 aqueous phase Substances 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 235000009508 confectionery Nutrition 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 239000012043 crude product Substances 0.000 description 1
- 239000003599 detergent Substances 0.000 description 1
- 239000000796 flavoring agent Substances 0.000 description 1
- 235000019634 flavors Nutrition 0.000 description 1
- 235000013305 food Nutrition 0.000 description 1
- ZXOFDLMHPUQRCE-UHFFFAOYSA-N hept-2-enylbenzene Chemical compound CCCCC=CCC1=CC=CC=C1 ZXOFDLMHPUQRCE-UHFFFAOYSA-N 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 238000010907 mechanical stirring Methods 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 239000012429 reaction media Substances 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 229910000104 sodium hydride Inorganic materials 0.000 description 1
- 239000012312 sodium hydride Substances 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- 229910052938 sodium sulfate Inorganic materials 0.000 description 1
- 235000011152 sodium sulphate Nutrition 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000000341 volatile oil 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
- C11B9/0061—Essential oils; Perfumes compounds containing a six-membered aromatic ring not condensed with another ring
Landscapes
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Wood Science & Technology (AREA)
- Organic Chemistry (AREA)
- Cosmetics (AREA)
- Detergent Compositions (AREA)
- Fats And Perfumes (AREA)
Priority Applications (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CH1541576A CH617851A5 (en) | 1976-12-08 | 1976-12-08 | Use of 5-oxa-2-methyl-7-phenyl-2-heptene as a fragrance |
| FR7734561A FR2373276A1 (fr) | 1976-12-08 | 1977-11-17 | Compositions odoriferantes |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CH1541576A CH617851A5 (en) | 1976-12-08 | 1976-12-08 | Use of 5-oxa-2-methyl-7-phenyl-2-heptene as a fragrance |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CH617851A5 true CH617851A5 (en) | 1980-06-30 |
Family
ID=4408899
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CH1541576A CH617851A5 (en) | 1976-12-08 | 1976-12-08 | Use of 5-oxa-2-methyl-7-phenyl-2-heptene as a fragrance |
Country Status (2)
| Country | Link |
|---|---|
| CH (1) | CH617851A5 (OSRAM) |
| FR (1) | FR2373276A1 (OSRAM) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4362657A (en) | 1980-09-30 | 1982-12-07 | International Flavors & Fragrances Inc. | Use of cyclohexyl phenethylether derivative in augmenting or enhancing the aromas of perfumes and colognes |
-
1976
- 1976-12-08 CH CH1541576A patent/CH617851A5/fr not_active IP Right Cessation
-
1977
- 1977-11-17 FR FR7734561A patent/FR2373276A1/fr active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| FR2373276B1 (OSRAM) | 1981-07-10 |
| FR2373276A1 (fr) | 1978-07-07 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PFA | Name/firm changed |
Owner name: ROURE S.A. |
|
| PL | Patent ceased | ||
| PL | Patent ceased |