| Weight | 136.238 g/mol |
|---|---|
| Formula | C10H16 |
| Hydrogen Acceptors | 0 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 0 |
TERPINOLENE (586-62-9)
4-isopropylidene-1-methylcyclohexene
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- Kinetics of the gas-phase reactions of OH and NO sub 3 radicals with 2-carene, 1,8-cineole, p-cymene, and terpinolene (Environmental Science & Technology, 1990)
- Monoterpenoid accumulation in 1,8-cineole, terpinolene and terpinen-4-ol chemotypes of Melaleuca alternifolia seedlings. (Phytochemistry, 2003)
- The monoterpene terpinolene from the oil of Pinus mugo L. in concert with -tocopherol and -carotene effectively prevents oxidation of LDL (Phytomedicine, 2005)
- Terpenoid metabolite profiling in Sitka spruce identifies association of dehydroabietic acid, (+)-3-carene, and terpinolene with resistance against white pine weevil (Botany, 2010)
- Specific introduction of an isopropylidene group in the synthesis of the monoterpene terpinolene and the sesquiterpene (+-)-.alpha.-curcumene (Journal of Organic Chemistry, 1974)
- Biotransformation of monoterpenoids, (-)- and (+)- menthols, terpinolene and carvotanacetone by Aspergillus species (Phytochemistry, 1991)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - H226: Flammable liquid and vapor
Warning Flammable liquids - Category 3 - H400: Very toxic to aquatic life
Warning Hazardous to the aquatic environment, acute hazard - Category 1 - 4-isopropylidene-1-methylcyclohexene
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SMILESCC1=CCC(=C(C)C)CC1
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InChIKeyMOYAFQVGZZPNRA-UHFFFAOYSA-N
- Pubchem - TERPINOLENE
- Wikipedia - terpinolene
The terpinenes are a group of isomeric hydrocarbons that are classified as terpenes. They each have the same molecular formula and carbon framework, but they differ in the position of carbon-carbon double bonds. -Terpinene has been isolated from cardamom and marjoram oils, and from other natural sources.
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