| Identification | Back Directory | [Name]
(+/-)-LAVANDULOL | [CAS]
1845-51-8 | [Synonyms]
(+/-)-LAVANDULOL
(+-)-LAVANDULOL TECHN. 90+%
5-methyl-2-prop-1-en-2-ylhex-4-en-1-ol
5-methyl-2-prop-1-en-2-yl-hex-4-en-1-ol
(+/-)-2-ISOPROPENYL-5-METHYL-4-HEXEN-1-OL | [EINECS(EC#)]
261-264-2 | [Molecular Formula]
C10H18O | [MDL Number]
MFCD00674532 | [MOL File]
1845-51-8.mol | [Molecular Weight]
154.25 |
| Chemical Properties | Back Directory | [Boiling point ]
203℃ | [density ]
0.878 g/mL at 20 °C(lit.) | [refractive index ]
n20/D 1.470 | [color ]
Colorless oily liquid | [Specific Gravity]
0.88 | [Odor]
Oily-herbaceous, warm-rosy odor |
| Hazard Information | Back Directory | [Chemical Properties]
Colorless oily liquid. Sp.Gr. 0.88. B.P. 203℃. Very slightly soluble in water, soluble in alcohol and oils.
| [Uses]
Lavandulol has found use in artificial Lavender oils, Lavandin, Bergamot, Clary Sage, etc. As a perfume material, it has not yet found much use, perhaps because of its price was always too high for its odor type, except in the case of the specific application in artificial essential oils.
| [Definition]
ChEBI: Lavandulol is a monoterpenoid alcohol that is hepta-1-5-diene which is substituted at positions 2 and 6 by methyl groups and at position 3 by a hydroxymethyl group. It is commonly found in lavender oil. It has a role as a fragrance, a pheromone and a plant metabolite. It is a monoterpenoid and a primary alcohol. | [Synthesis Reference(s)]
Tetrahedron, 47, p. 9727, 1991 DOI: 10.1016/S0040-4020(01)80712-2
Tetrahedron Letters, 23, p. 933, 1982 | [Synthesis]
Lavandulol can be synthesized by the following two methods:
1) from Isoprene hydrobromide plus Sodium iso-propylidene malonic ester via Lavandulic acid.
2) from Methylheptenone plus Formaldehyde in a Prins' reaction followed by a Methyl Grignard reaction or a pyrolysis.
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Leancare Ltd.
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SIGMA-RBI
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