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Ethyl decanoate

From Wikipedia, the free encyclopedia
Ethyl decanoate
Names
Preferred IUPAC name
Ethyl decanoate
Other names
Decanoic acid ethyl ester
Ethyl caprate
Ethyl caprinate
Ethyl decylate
Capric acid ethyl ester
Identifiers
3D model (JSmol)
ChemSpider
ECHA InfoCard 100.003.421 Edit this at Wikidata
UNII
  • InChI=1S/C12H24O2/c1-3-5-6-7-8-9-10-11-12(13)14-4-2/h3-11H2,1-2H3
    Key: RGXWDWUGBIJHDO-UHFFFAOYSA-N
  • InChI=1/C12H24O2/c1-3-5-6-7-8-9-10-11-12(13)14-4-2/h3-11H2,1-2H3
    Key: RGXWDWUGBIJHDO-UHFFFAOYAS
  • O=C(OCC)CCCCCCCCC
Properties
C12H24O2
Molar mass 200.322 g·mol−1
Density 0.862 g/cm3
Melting point −26 °C (−15 °F; 247 K)
Boiling point 245 °C (473 °F; 518 K)
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

Ethyl decanoate, also known as ethyl caprate, is a fatty acid ester formed from capric acid and ethanol. This ester is a frequent product of fermentation during winemaking, especially at temperatures above 15 °C.[1]

References

[edit]
  1. ^ Killian, E.; Ough, C. S. (1979). "Fermentation Esters — Formation and Retention as Affected by Fermentation Temperature". American Journal of Enology and Viticulture. 30 (4): 301–305.