| Identification | Back Directory | [Name]
7-OCTEN-2-OL, 2-METHYL-6-METHYLENE | [CAS]
543-39-5 | [Synonyms]
MYCENOL5
MYRCENOL
2H MYRCENOL
MYRCENOL 50
MYRCENOL 50 IN D.E.P.
2-Methyl-6-methylenoct-7-en-2-ol
2-methyl-6-methylene-7-octen-2-o
2-Methyl-6-methylene-7-octen-2-ol
3-Methylene-7-methyl-1-octen-7-ol
2-methyl-6-methyleneoct-7-en-2-ol
7-OCTEN-2-OL, 2-METHYL-6-METHYLENE
2-methyl-6-methylideneoct-7-en-2-ol
2-methyl-6-methylidene-oct-7-en-2-ol | [EINECS(EC#)]
208-843-8 | [Molecular Formula]
C10H18O | [MDL Number]
MFCD00128271 | [MOL File]
543-39-5.mol | [Molecular Weight]
154.25 |
| Hazard Information | Back Directory | [Chemical Properties]
It is a colorless liquid
with a fresh, floral, slightly lime-like odor. Due to its conjugated double bonds, it
tends to polymerize; polymerization can be suppressed by adding inhibitors (e.g.,
antioxidants such as BHT).
Myrcenol can be prepared by treating myrcene with diethylamine to give a mixture
of geranyl- and neryldiethylamine. These compounds are hydrated with a
dilute acid to the corresponding hydroxydiethylamines. Deamination tomyrcenol
is effected by using a palladium–phosphine–cation complex as a catalyst.
Myrcenol is used in perfumery to obtain a lifting top note in citrus and lavender
compositions. It is mainly important in the production of 4-(4-hydroxy-4-
methylpentyl)-3-cyclohexenecarboxaldehyde. | [Definition]
ChEBI: A monoterpenoid that is oct-7-en-2-ol substituted by a methyl group at position 2 and a methylidene group at position 6 respectively. |
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