ethyl hexanoate
{{chembox
| Verifiedfields = changed
| Watchedfields = changed
| verifiedrevid =
| Name = Ethyl hexanoate
| ImageFile =Ethyl-hexanoate.svg
| ImageName =
| PIN = Ethyl hexanoate
| OtherNames = Ethyl caproate
Caproic acid ethyl ester
|Section1={{Chembox Identifiers
| CASNo_Ref = {{cascite|correct|CAS}}
| CASNo = 123-66-0
| UNII_Ref = {{fdacite|correct|FDA}}
| UNII = FLO6YR1SHT
| PubChem = 31265
| ChemSpiderID = 29005
| SMILES = CCCCCC(=O)OCC
| InChI = 1/C8H16O2/c1-3-5-6-7-8(9)10-4-2/h3-7H2,1-2H3
| InChIKey = SHZIWNPUGXLXDT-UHFFFAOYAA
| ChEBI_Ref =
| ChEBI =
| StdInChI_Ref = {{stdinchicite|changed|chemspider}}
| StdInChI = 1S/C8H16O2/c1-3-5-6-7-8(9)10-4-2/h3-7H2,1-2H3
| StdInChIKey_Ref = {{stdinchicite|changed|chemspider}}
| StdInChIKey = SHZIWNPUGXLXDT-UHFFFAOYSA-N
}}
|Section2={{Chembox Properties
| C=8 | H=16 | O=2
| Appearance = Colorless liquid{{GESTIS|ZVG=32110}}
| MeltingPtC = -67
| BoilingPtC = 168
}}
}}
Ethyl hexanoate is the ester resulting from the condensation of hexanoic acid and ethanol. It has fruity aroma similar to apple peel.{{cite journal | vauthors = Zheng LY, Sun GM, Liu YG, Lv LL, Yang WX, Zhao WF, Wei CB | title = Aroma volatile compounds from two fresh pineapple varieties in China | journal = International Journal of Molecular Sciences | volume = 13 | issue = 6 | pages = 7383–92 | date = 2012-06-14 | pmid = 22837701 | pmc = 3397533 | doi = 10.3390/ijms13067383 | doi-access = free }}