// Workers AI · dad joke modeWhat did phenethyl benzoate say? "I'm bonded to you.
| Names | |
|---|---|
| IUPAC name
2-Phenylethyl benzoate | |
Other names
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| Identifiers | |
3D model (JSmol) |
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| ChEBI | |
| ChEMBL | |
| ChemSpider | |
| ECHA InfoCard | 100.002.124 |
| EC Number |
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PubChem CID |
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| UNII | |
CompTox Dashboard (EPA) |
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| Properties | |
| C15H14O2 | |
| Molar mass | 226.275 g·mol−1 |
| Appearance | colorless to yellowish[1] |
| Odor | floral, rose, honey[1] |
| Density | 1.092 g/cm3 |
| Boiling point | 329 °C (624 °F; 602 K) |
| sparingly soluble | |
| Solubility | soluble in ethanol, diethyl ether, chloroform and most organic solvents |
| log P | 4.01[2] |
| Hazards | |
| GHS labelling:[2] | |
| Warning | |
| H411 | |
| P273, P391, P501 | |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Phenethyl benzoate is an organic compound, an ester of benzoic acid and phenethyl alcohol.
Ocurrence
[edit]Phenethyl benzoate is found naturally in several plants, including bilberry (Vaccinium myrtillus), cinnamon leaf (Cinnamomum zeylancium), cassia leaf (Cinnamomum cassia), and sea buckthorn (Hippophae rhamnoides).[1] It is also found in essential oil from flowers of rose and orange.[1]
Synthesis
[edit]Phenethyl benzoate can be obtained by the Schotten–Baumann reaction of phenethyl alcohol and benzoyl chloride in the presence of NaOH, transesterification of phenethyl alcohol and methyl benzoate, or acid-catalyzed Fischer–Speier esterification of phenethyl alcohol with benzoic acid.[1]
Usage
[edit]Phenethyl benzoate is used as a fragrance agent in the manufacture of perfumes and cosmetics.
References
[edit]- 1 2 3 4 5 Burdock, George A. (1997). Encyclopedia of Food and Color Additives. CRC Press. p. 2157. ISBN 978-0-8493-9414-0.
- 1 2 PubChem. "Phenethyl Benzoate". pubchem.ncbi.nlm.nih.gov. Retrieved 2026-09-26.
Further reading
[edit]- Burdock, George A. (2016-04-19). Fenaroli's Handbook of Flavor Ingredients. CRC Press. p. 1635. ISBN 978-1-4200-9086-4.
