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BOC Sciences |
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| | LAVANDULOL Basic information |
| Product Name: | LAVANDULOL | | Synonyms: | (-)-4-hexen-1-o;(r)-4-hexen-1-o;(r)-5-methyl-2-(1-methylethenyl)-4-hexen-1-ol;(theta)-4-hexen-1-o;4-Hexen-1-ol, 2-isopropenyl-5-methyl-, (-)-;4-Hexen-1-ol, 5-methyl-2-(1-methylethenyl)-, (R)-;LAVANDULOL;(2R)-2-Isopropenyl-5-methyl-4-hexene-1-ol | | CAS: | 498-16-8 | | MF: | C10H18O | | MW: | 154.25 | | EINECS: | | | Product Categories: | | | Mol File: | 498-16-8.mol |  |
| | LAVANDULOL Chemical Properties |
| Boiling point | 94-95 °C(Press: 13 Torr) | | density | 0.8742 g/cm3(Temp: 17.54 °C) | | pka | 14.81±0.10(Predicted) | | Odor | at 10.00%indipropylene glycol. herbal | | LogP | 2.665 (est) |
| | LAVANDULOL Usage And Synthesis |
| Uses | (-)-Lavandulol is the isomer of (±)-Lavandulol (HY-N7731). (±)-Lavandulol is an irregular monoterpene alcohol. (±)-Lavandulol can be transformed by a fungal strain Rhizopus oryzae into corresponding oxygenated metabolite[1]. | | Definition | ChEBI: 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. | | References | [1] Daramwar PP, et al. Transformation of (±)-lavandulol and (±)-tetrahydrolavandulol by a fungal strain Rhizopus oryzae. Bioresour Technol. 2012 Jul;115:70-4. DOI:10.1016/j.biortech.2011.11.038 |
| | LAVANDULOL Preparation Products And Raw materials |
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