Dihydromyrcenol
From Wikipedia, the free encyclopedia
| Names | |
|---|---|
| IUPAC name
2,6-Dimethyloct-7-en-2-ol | |
| Identifiers | |
3D model (JSmol) |
|
| ChEBI | |
| ChEMBL | |
| ChemSpider | |
| DrugBank | |
| ECHA InfoCard | 100.038.497 |
PubChem CID |
|
| UNII | |
CompTox Dashboard (EPA) |
|
| |
| |
| Properties | |
| C10H20O | |
| Molar mass | 156.269 g·mol−1 |
| Appearance | Colorless viscous liquid[1] |
| Density | 0.832 g/cm3 (20 °C)[1] |
| Boiling point | 194–197 °C (381–387 °F; 467–470 K)[1] |
| 0.939 g/L (20 °C)[1] | |
| Hazards | |
| Flash point | 76 °C (169 °F; 349 K)[1] |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
| |
Dihydromyrcenol is a synthetic organic compound used primarily as a fragrance ingredient. Despite its similarity to some natural compounds of the monoterpene class, such as myrcenol, it has not been reported to be found in nature.[2]
Odor and uses
Dihydromyrcenol is extensively used in the fragrance industry for its fresh lime and citrus-like odor.[2] Descriptions of its scent include citrus type,[4] lime-like citrusy-floral sweet with considerable tenacity,[2] fresh citrus-like with a lavender note,[5] fresh cool metallic lime citrus floral bergamot,[6] and lavender fragrance reminiscent of lemon.[7] Worldwide use exceeded 1000 metric tons per year as of 2004.[5]
