| Identification | Back Directory | [Name]
Ebanol | [CAS]
67801-20-1 | [Synonyms]
EBANOL
Ebony alcohol
sandal pentenol
Einecs 267-140-4
Muscosandrol/Ebanol
Ebanol ISO 9001：2015 REACH
METHYL-3-(TRIMETHYL-2,2,3-CYCLOPENTEN-3-YL-1)-5-PENTANOL-2
3-Methyl-5-(2,2,3-trimethyl-3-cyclopentenyl)-4-pentene-2-ol
3-methyl-5-(2,2,3-trimethyl-3-cyclopenten-1-yl)-4-penten-2-o
3-methyl-5-(2,2,3-trimethyl-3-cyclopenten-1-yl)-4-penten-2-ol
3-Methyl-5-(2,2,3-trimethyl-3-cyclopenten-1-yl)pent-4-en-2-ol
3-METHYL-5-(2,2,3-TRIMETHYLCYCLOPENT-3-EN-1-YL)PENT-4-EN-2-OL
4-Penten-2-ol, 3-methyl-5-(2,2,3-trimethyl-3-cyclopenten-1-yl)-
(Z)-3-methyl-5-(2,2,3-trimethylcyclopent-3-en-1-yl)pent-4-en-2-ol
3-METHYL-5-(2,2,3-TRIMETHYL-3-CYCLOPENTEN-1-YL)-4-PENTEN-2-OL,92%, GLC
3-Methyl-5-(2,2,3-trimethyl-3-cyclopenten-1-yl)-4-penten-2-ol ( isomer) | [EINECS(EC#)]
267-140-4 | [Molecular Formula]
C14H24O | [MDL Number]
MFCD00672177 | [MOL File]
67801-20-1.mol | [Molecular Weight]
208.34 |
| Hazard Information | Back Directory | [Chemical Properties]
Ebanol is a mixture of isomers. It is a pale yellow liquid with a powerful
woody, sandalwood odor withmusk aspect.Thematerial is obtained by aldol
condensation of α-campholenaldehyde with 2-butanone. Subsequent isomerization
of the double bond with potassium tert-butylate leads to a ??,??-unsaturated
ketone, which is reduced with NaBH4 to yield a mixture of chiefly four diastereomeric
alcohols. Alternatively, the ??,??-unsaturated ketone can be prepared
by dehydration of the ketol, which is obtained when the aldol reaction is performed
under special reaction conditions.
It is used in fine fragrances as well as in functional products. | [Flammability and Explosibility]
Nonflammable | [Trade name]
Ebanol® (Givaudan) |
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