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| Product Name: | Ebanol | | Synonyms: | 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;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;3-Methyl-5-(2,2,3-trimethyl-3-cyclopenten-1-yl)-4-penten-2-ol ( isomer) | | CAS: | 67801-20-1 | | MF: | C14H24O | | MW: | 208.34 | | EINECS: | 267-140-4 | | Product Categories: | | | Mol File: | 67801-20-1.mol |  |
| | Ebanol Chemical Properties |
| | Ebanol Usage And Synthesis |
| 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. | | Uses | 3-Methyl-5-(2,2,3-trimethyl-3-cyclopenten-1-yl)-4-penten-2-ol may be used as an analytical standard for the determination of the analyte in sandalwood oil (Santalum album L.), cosmetics and personal care products, and biological samples of the animals exposed to the sandalwood odorants by gas chromatography (GC) based techniques. | | Flammability and Explosibility | Non flammable | | Trade name | Ebanol® (Givaudan) |
| | Ebanol Preparation Products And Raw materials |
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