Date published: 2025-10-6

1-800-457-3801

SCBT Portrait Logo
Seach Input

Ethyl heptanoate (CAS 106-30-9)

0.0(0)
Write a reviewAsk a question

Alternate Names:
Ethyl enanthate
Application:
Ethyl heptanoate is an aromatic compound resembling grape
CAS Number:
106-30-9
Molecular Weight:
158.24
Molecular Formula:
C9H18O2
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

QUICK LINKS

Ethyl heptanoate, a chemical compound with the molecular formula C9H18O2, has been extensively studied in scientific research, particularly in the fields of organic chemistry, flavor chemistry, and fragrance science. It is an ester that possesses a fruity, sweet aroma. Research has focused on investigating the synthesis of ethyl heptanoate and understanding its mechanisms of formation. Ethyl heptanoate can be synthesized through esterification reactions between ethanol and heptanoic acid, catalyzed by acid catalysts or enzymes. Studies have explored the factors influencing the yield and selectivity of ethyl heptanoate synthesis, such as reaction conditions, catalysts, and reaction kinetics. Furthermore, ethyl heptanoate has been used as a flavoring agent and fragrance ingredient. Research has examined its sensory properties, odor thresholds, and contributions to aroma profiles. Ethyl heptanoate is commonly employed to impart fruity and pineapple-like notes in various products. Additionally, its use as a solvent in organic synthesis has been investigated. The research applications of ethyl heptanoate contribute to advancements in organic chemistry, flavor formulation, and fragrance science. By exploring the mechanisms and applications of ethyl heptanoate, researchers aim to optimize its synthesis methods, develop new organic transformations, and gain insights into its sensory impact and potential applications in various industries.


Ethyl heptanoate (CAS 106-30-9) References

  1. Identification of aroma compounds in Parmigiano-Reggiano cheese by gas chromatography/olfactometry.  |  Qian, M. and Reineccius, G. 2002. J Dairy Sci. 85: 1362-9. PMID: 12146465
  2. Odor detection of single chemicals and binary mixtures.  |  Cometto-Muñiz, JE., et al. 2005. Behav Brain Res. 156: 115-23. PMID: 15474656
  3. Volatile flavor compounds, total polyphenolic contents and antioxidant activities of a China gingko wine.  |  Wang, X., et al. 2015. Food Chem. 182: 41-6. PMID: 25842306
  4. Multivariate relationships among sensory, physicochemical parameters, and targeted volatile compounds in commercial red sufus (Chinese fermented soybean curd): Comparison of QDA® and Flash Profile methods.  |  He, W. and Chung, HY. 2019. Food Res Int. 125: 108548. PMID: 31554058
  5. RIFM fragrance ingredient safety assessment, ethyl heptanoate, CAS Registry Number 106-30-9.  |  Api, AM., et al. 2021. Food Chem Toxicol. 156 Suppl 1: 112501. PMID: 34389371
  6. Enzymatic Characterization of Purified β-Glucosidase from Non-Saccharomyces Yeasts and Application on Chardonnay Aging.  |  Gao, P., et al. 2022. Foods. 11: PMID: 35327274
  7. Characterization and correlation of dominant bacteria and volatile compounds in post-fermentation process of Ba-bao Douchi.  |  Zhang, YZ., et al. 2022. Food Res Int. 160: 111688. PMID: 36076449
  8. Olfactory Responses of Anastrepha obliqua (Diptera: Tephritidae) to Mango Fruits as Influenced by Cultivar and Ripeness Stages.  |  Neri Benítez-Herrera, L., et al. 2023. Environ Entomol. 52: 210-216. PMID: 36852867
  9. Flavor evolution of normal- and low-fat Chinese sausage during natural fermentation.  |  Xing, B., et al. 2023. Food Res Int. 169: 112937. PMID: 37254361
  10. Identification of regionalmarkers based on the flavor molecular matrix analysis of sauce-aroma style baijiu.  |  Huang, H., et al. 2023. J Sci Food Agric. 103: 7434-7444. PMID: 37395138

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Ethyl heptanoate, 100 ml

sc-214992
100 ml
$31.00