Product Name: |
Ebanol |
Synonyms: |
3-methyl-5-(2,2,3-trimethyl-3-cyclopenten-1-yl)-4-penten-2-o;EBANOL;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;4-Penten-2-ol, 3-methyl-5-(2,2,3-trimethyl-3-cyclopenten-1-yl)-;METHYL-3-(TRIMETHYL-2,2,3-CYCLOPENTEN-3-YL-1)-5-PENTANOL-2;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-cyclopentenyl)-4-pentene-2-ol |
CAS: |
67801-20-1 |
MF: |
C14H24O |
MW: |
208.34 |
EINECS: |
267-140-4 |
Product Categories: |
|
Mol File: |
67801-20-1.mol |
|
Boiling point |
287°C |
density |
0.938 |
FEMA |
4775 | 3-METHYL-5-(2,2,3-TRIMETHYLCYCLOPENT-3-EN-1-YL)PENT-4-EN-2-OL |
Fp |
103°C |
pka |
14.96±0.20(Predicted) |
JECFA Number |
2220 |
EPA Substance Registry System |
4-Penten-2-ol, 3-methyl-5-(2,2,3-trimethyl-3-cyclopenten-1-yl)- (67801-20-1) |
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. |
Trade name |
Ebanol® (Givaudan) |