Ethyl octanoate
| Names | |
|---|---|
| Preferred IUPAC name
Ethyl octanoate | |
| Other names
Ethyl caprylate
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| Identifiers | |
3D model (JSmol)
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| ChemSpider | |
| ECHA InfoCard | 100.003.078 |
| EC Number | |
PubChem CID
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| UNII | |
CompTox Dashboard (EPA)
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| Properties | |
| C10H20O2 | |
| Molar mass | 172.268 g·mol−1 |
| Density | 0.86215 g/cm3 |
| Melting point | −48 °C (−54 °F; 225 K) |
| Boiling point | 208 °C (406 °F; 481 K) |
| 70.1 mg/L | |
| Vapor pressure | 0.2 mbar at 20 °C; 3.18 mbar at 60 °C |
| Viscosity | 1.411 mPa·s |
| Hazards | |
| Flash point | 79 °C (174 °F; 352 K) |
| 325 °C (617 °F; 598 K) | |
| Explosive limits | 0.7 - Vol.% |
| Lethal dose or concentration (LD, LC): | |
LD50 (median dose)
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25.96 g/kg (rat, oral) |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references
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Ethyl octanoate, also known as ethyl caprylate, is a fatty acid ester formed from caprylic acid and ethanol. A colorless liquid at room temperature, it has the semi-developed formula of CH3(CH2)6COOCH2CH3, and is used in food industries as a flavoring and in the perfume industry as a scent additive. It is present in many fruits and alcoholic beverages, and has a strong odor of fruit and flowers.