Date published: 2025-10-14

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Ethyl octanoate (CAS 106-32-1)

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Alternate Names:
Caprylic acid ethyl ester
CAS Number:
106-32-1
Purity:
99%
Molecular Weight:
172.26
Molecular Formula:
C10H20O2
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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Ethyl octanoate, a chemical compound with the molecular formula C10H20O2, has been the subject of scientific research, particularly in the fields of organic chemistry, flavor chemistry, and environmental sciences. It is an ester that exhibits a fruity, apple-like aroma. Research has focused on investigating the synthesis of ethyl octanoate and understanding its mechanisms of formation. Ethyl octanoate can be synthesized through esterification reactions between ethanol and octanoic acid, catalyzed by acid catalysts or enzymes. Studies have explored the factors influencing the yield and selectivity of ethyl octanoate synthesis, such as reaction conditions, catalysts, and reaction kinetics. Furthermore, ethyl octanoate has been extensively used as a flavoring agent and fragrance ingredient. Research has examined its sensory properties, odor thresholds, and contributions to aroma profiles. Ethyl octanoate is commonly employed to impart fruity and apple-like notes in various products. Additionally, its use as a solvent in organic synthesis has been investigated. The research applications of ethyl octanoate contribute to advancements in organic chemistry, flavor formulation, and understanding the behavior of volatile organic compounds (VOCs). By exploring the mechanisms and applications of ethyl octanoate, researchers aim to optimize its synthesis methods, develop new organic transformations, and gain insights into its sensory impact and environmental fate.


Ethyl octanoate (CAS 106-32-1) References

  1. Parameters affecting ethyl ester production by Saccharomyces cerevisiae during fermentation.  |  Saerens, SM., et al. 2008. Appl Environ Microbiol. 74: 454-61. PMID: 17993562
  2. Quantitative ester analysis in cachaca and distilled spirits by gas chromatography-mass spectrometry (GC-MS).  |  Nascimento, ES., et al. 2008. J Agric Food Chem. 56: 5488-93. PMID: 18570431
  3. Changes in volatile composition and sensory attributes of wines during alcohol content reduction.  |  Longo, R., et al. 2017. J Sci Food Agric. 97: 8-16. PMID: 27098726
  4. Spectroscopy reveals that ethyl esters interact with proteins in wine.  |  Di Gaspero, M., et al. 2017. Food Chem. 217: 373-378. PMID: 27664648
  5. Characterization of Qingke Liquor Aroma from Tibet.  |  Qian, YL., et al. 2019. J Agric Food Chem. 67: 13870-13881. PMID: 31544459
  6. Beer volatile fingerprinting at different brewing steps.  |  Alves, V., et al. 2020. Food Chem. 326: 126856. PMID: 32450481
  7. Aromatypicity of Austrian Pinot Blanc Wines.  |  Philipp, C., et al. 2020. Molecules. 25: PMID: 33287238
  8. Isolation and Identification of a High-Yield Ethyl Caproate-Producing Yeast From Daqu and Optimization of Its Fermentation.  |  Fan, G., et al. 2021. Front Microbiol. 12: 663744. PMID: 34135875
  9. RIFM fragrance ingredient safety assessment, ethyl octanoate, CAS Registry Number 106-32-1.  |  Api, AM., et al. 2021. Food Chem Toxicol. 156 Suppl 1: 112500. PMID: 34389370
  10. Characterization of Odorants in a 10-Year-Old Riesling Wine.  |  Dein, M., et al. 2021. J Agric Food Chem. 69: 11372-11381. PMID: 34547201

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Ethyl octanoate, 5 g

sc-214994
5 g
$20.00

Ethyl octanoate, 100 g

sc-214994A
100 g
$36.00