ethyl salicylate
{{chembox
| Watchedfields = changed
| verifiedrevid = 417939820
| Name = Ethyl salicylate{{cite web|url=https://pubchem.ncbi.nlm.nih.gov/compound/Ethyl_salicylate|title=Ethyl salicylate|last=Pubchem|website=pubchem.ncbi.nlm.nih.gov|accessdate=25 February 2018}}
| ImageFile = Ethyl salicylate.png
| ImageSize = 160
| ImageAlt = Structural formula of ethyl salicylate
| ImageFile1 = Ethyl salicylate 3D ball.png
| ImageAlt1 = Ball-and-stick model of the ethyl salicylate molecule
| PIN = Ethyl 2-hydroxybenzoate
|Section1={{Chembox Identifiers
| ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}}
| ChemSpiderID = 21105897
| PubChem = 8365
| UNII_Ref = {{fdacite|correct|FDA}}
| UNII = 555U6TZ2MV
| InChI = 1/C9H10O3/c1-2-12-9(11)7-5-3-4-6-8(7)10/h3-6,10H,2H2,1H3
| InChIKey = GYCKQBWUSACYIF-UHFFFAOYAH
| StdInChI_Ref = {{stdinchicite|correct|chemspider}}
| StdInChI = 1S/C9H10O3/c1-2-12-9(11)7-5-3-4-6-8(7)10/h3-6,10H,2H2,1H3
| StdInChIKey_Ref = {{stdinchicite|correct|chemspider}}
| StdInChIKey = GYCKQBWUSACYIF-UHFFFAOYSA-N
| CASNo_Ref = {{cascite|correct|CAS}}
| CASNo = 118-61-6
| SMILES = O=C(OCC)c1ccccc1O
}}
|Section2={{Chembox Properties
| C=9|H=10|O=3
| Appearance = Colorless liquid{{GESTIS|ZVG=101953}}
| MeltingPtC = 1.3
| BoilingPtC = 232
}}
}}
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.{{cite journal | doi = 10.1016/j.fct.2007.09.043| pmid = 18023517| title = Fragrance material review on ethyl salicylate| journal = Food and Chemical Toxicology| volume = 45| pages = S397–401| year = 2007| last1 = Lapczynski| first1 = A| last2 = McGinty| first2 = D| last3 = Jones| first3 = L| last4 = Bhatia| first4 = S| last5 = Letizia| first5 = C.S| last6 = Api| first6 = A.M}}
See also
References
{{Salicylates}}
{{DEFAULTSORT:Ethyl Salicylate}}
{{ester-stub}}