Ethyl salicylate
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| Names | |
|---|---|
| Preferred IUPAC name
Ethyl 2-hydroxybenzoate | |
| Identifiers | |
3D model (JSmol) |
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| ChemSpider | |
| ECHA InfoCard | 100.003.878 |
PubChem CID |
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| UNII | |
CompTox Dashboard (EPA) |
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| Properties | |
| C9H10O3 | |
| Molar mass | 166.176 g·mol−1 |
| Appearance | Colorless liquid[2] |
| Odor | wintergreen[3] |
| Density | 1.13 g/cm3[2] |
| Melting point | 1.3 °C (34.3 °F; 274.4 K)[2] |
| Boiling point | 232 °C (450 °F; 505 K)[2] |
| Hazards | |
| GHS labelling: | |
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| Warning | |
| H302 | |
| P264, P270, P301+P317, P330, P501 | |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references | |
Ethyl salicylate is the ester formed by the condensation of salicylic acid and ethanol. It is a clear liquid that is sparingly soluble in water, but soluble in alcohol and ether. It has a pleasant odor resembling wintergreen and is used in perfumery and artificial flavors.[3] More specifically, its aroma is described as "sweet, wintergreen, minty, floral, spicy, balsamic, tutti frutti, cooling".[4]
See also
References
- ↑ Pubchem. "Ethyl salicylate". pubchem.ncbi.nlm.nih.gov. Retrieved 25 February 2018.
- 1 2 3 4 Record in the GESTIS Substance Database of the Institute for Occupational Safety and Health
- 1 2 Lapczynski, A; McGinty, D; Jones, L; Bhatia, S; Letizia, C.S; Api, A.M (2007). "Fragrance material review on ethyl salicylate". Food and Chemical Toxicology. 45: S397–401. doi:10.1016/j.fct.2007.09.043. PMID 18023517.
- ↑ "ethyl salicylate". Scents and Flavors. Scents and Flavors. Retrieved 1 April 2026.


