| 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) |