Date published: 2025-10-18

1-800-457-3801

SCBT Portrait Logo
Seach Input

Ethyl decanoate (CAS 110-38-3)

0.0(0)
Write a reviewAsk a question

See product citations (1)

Alternate Names:
Capric acid ethyl ester; Ethyl caprate
CAS Number:
110-38-3
Purity:
99%
Molecular Weight:
200.32
Molecular Formula:
C12H24O2
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

QUICK LINKS

Ethyl decanoate, an organic compound with the molecular formula C12H24O2, has been extensively studied in scientific research, particularly in the fields of organic chemistry, materials science, and flavor development. Research has focused on elucidating the mechanisms of ethyl decanoate synthesis and its diverse applications. Ethyl decanoate can be synthesized through the esterification of decanoic acid with ethanol, typically in the presence of an acid catalyst. Studies have explored the factors influencing the yield and selectivity of ethyl decanoate synthesis, such as reaction conditions, catalysts, and reaction kinetics. Furthermore, ethyl decanoate has been widely used as a flavoring agent in the food and beverage industry. Research has investigated its role in providing fruity and sweet notes, enhancing the sensory experience of various food products. Additionally, ethyl decanoate has been utilized in the development of novel materials, such as coatings, adhesives, and lubricants. Its unique chemical properties have been harnessed to modify material characteristics, including surface properties, viscosity, and tribological behavior. The research applications of ethyl decanoate contribute to advancements in organic synthesis, materials science, and the creation of functional compounds. By exploring the mechanisms and applications of ethyl decanoate, researchers aim to optimize its synthesis methods, discover new flavor combinations, and explore its potential utilization in various industries.


Ethyl decanoate (CAS 110-38-3) References

  1. Ethyl decanoate as a major component in the defensive secretion of two new zealand aleocharine (staphylinidae) beetles-Tramiathaea cornigera (broun) andThamiaraea fuscicornis (broun).  |  Gnanasunderam, C., et al. 1981. J Chem Ecol. 7: 197-202. PMID: 24420439
  2. Effects of Basal Defoliation on Wine Aromas: A Meta-Analysis.  |  Wang, Y., et al. 2018. Molecules. 23: PMID: 29597302
  3. Characterizing the chemical and sensory profiles of traditional American meads.  |  Senn, K., et al. 2021. J Food Sci. 86: 1048-1057. PMID: 33527386
  4. Comparative metabolome and transcriptome analyses of the properties of Kluyveromyces marxianus and Saccharomyces yeasts in apple cider fermentation.  |  Zhang, Z., et al. 2022. Food Chem (Oxf). 4: 100095. PMID: 35415699
  5. RIFM fragrance ingredient safety assessment, ethyl decanoate, CAS Registry Number 110-38-3.  |  Api, AM., et al. 2022. Food Chem Toxicol. 167 Suppl 1: 113319. PMID: 35872255
  6. The impact of indigenous Saccharomyces cerevisiae and Schizosaccharomyces japonicus on typicality of crystal grape (Niagara) wine.  |  Wang, C., et al. 2022. Food Res Int. 159: 111580. PMID: 35940784
  7. Effect of low temperature on the shaping of yeast-derived metabolite compositions during wine fermentation.  |  Du, Q., et al. 2022. Food Res Int. 162: 112016. PMID: 36461241
  8. Capture of Fermentation Gas from Fermentation of Grape Must.  |  Prusova, B., et al. 2023. Foods. 12: PMID: 36766103
  9. Application of Schizosaccharomyces japonicus in makgeolli fermentation and its brewing characteristics.  |  Choi, J., et al. 2023. Food Sci Biotechnol. 32: 1383-1393. PMID: 37457408
  10. Enhancing blueberry wine aroma: Insights from cultivar selection and berry sorting.  |  Wang, Y., et al. 2023. Curr Res Food Sci. 7: 100643. PMID: 38077470

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Ethyl decanoate, 100 g

sc-214989
100 g
$60.00

Ethyl decanoate, 500 g

sc-214989A
500 g
$90.00