| Names | |
|---|---|
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IUPAC name
(E)-1-(2,6,6-Trimethyl-1-cyclohexenyl)but-2-en-1-one
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| Other names
Rose ketones
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| Identifiers | |
|
23726-91-2 |
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| 3D model (Jmol) | Interactive image |
| ChemSpider |
4524302 |
| ECHA InfoCard | 100.041.660 |
| PubChem | 5374527 |
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| Properties | |
| C13H20O | |
| Molar mass | 192.30 g/mol |
| Density | 0.934 g/mL |
| Hazards | |
| R-phrases | R43 |
| S-phrases | S36/37 |
|
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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| Infobox references | |
| Names | |
|---|---|
|
IUPAC name
(E)-1-(2,6,6-trimethyl-1-cyclohex-2-enyl)but-2-en-1-one
|
|
| Other names
Rose ketones
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|
| Identifiers | |
|
24720-09-0 |
|
| 3D model (Jmol) | Interactive image |
| ChemSpider | 4518000 |
| ECHA InfoCard | 100.041.660 |
| PubChem | 5366077 |
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|
|
|
| Properties | |
| C13H20O | |
| Molar mass | 192.30 g·mol−1 |
|
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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| Infobox references | |
Damascones are a series of closely related chemical compounds that are components of a variety of essential oils. The damascones belong to a family of chemicals known as rose ketones, which also includes damascenones and ionones. beta-Damascone is a contributor to the aroma of roses, despite its relatively low concentration, and is an important fragrance chemical used in perfumery.
The damascones are derived from the degradation of carotenoids.