Date published: 2025-10-3

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Ethyl Heptadecanoate (CAS 14010-23-2)

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Alternate Names:
Ethyl Margarate; Heptadecanoic Acid Ethyl Ester; Margaric Acid Ethyl Ester
CAS Number:
14010-23-2
Purity:
≥97%
Molecular Weight:
298.51
Molecular Formula:
C19H38O2
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 Heptadecanoate, with the CAS number 14010-23-2, is an organic compound classified as a fatty acid ester—specifically, the ethyl ester of heptadecanoic acid (margaric acid). This compound consists of a long carbon chain (C17) with a carboxylic acid esterified with ethanol at one end, resulting in a non-polar, lipid-like molecule with distinct chemical properties. In research, Ethyl Heptadecanoate is primarily used within the domain of analytical chemistry, where it serves as a standard or reference material in gas chromatography and mass spectrometry. These techniques benefit from its stability and distinct mass spectral characteristics, making it ideal for calibrating instruments and developing methodologies for the analysis of fatty acid esters and related compounds. Additionally, Ethyl Heptadecanoate is utilized in studies related to lipid chemistry, particularly in understanding the physical properties of fatty acid esters, such as melting and boiling points, solubility, and interactions with other lipids. Its structure and properties also make it a candidate for use in the synthesis of bio-based materials, where researchers explore the potential of fatty acid esters as components of environmentally friendly plastics, lubricants, and coatings. The application of Ethyl Heptadecanoate in these diverse fields highlights its utility in both fundamental and applied chemical research, providing insights into the behavior of lipid molecules and aiding in the development of new materials and analytical techniques.


Ethyl Heptadecanoate (CAS 14010-23-2) References

  1. Stearic acid stimulates FA ethyl ester synthesis in HepG2 cells exposed to ethanol.  |  Hasaba, A., et al. 2003. Lipids. 38: 1051-5. PMID: 14669970
  2. Fatty acid ethyl esters, nonoxidative ethanol metabolites, synthesis, uptake, and hydrolysis by human platelets.  |  Salem, RO., et al. 2005. Biochim Biophys Acta. 1738: 99-104. PMID: 16325465
  3. Rapid, accurate, and sensitive fatty acid ethyl ester determination by gas chromatography-mass spectrometry.  |  Kulig, CC., et al. 2006. J Lab Clin Med. 147: 133-8. PMID: 16503243
  4. Liquid chromatography-tandem mass spectrometry for fatty acid ethyl esters in meconium: assessment of prenatal exposure to alcohol in two European cohorts.  |  Pichini, S., et al. 2008. J Pharm Biomed Anal. 48: 927-33. PMID: 18786798
  5. Quantitation of fatty acid ethyl esters in human meconium by an improved liquid chromatography/tandem mass spectrometry.  |  Kwak, HS., et al. 2010. J Chromatogr B Analyt Technol Biomed Life Sci. 878: 1871-4. PMID: 20605750
  6. Efficient determination of six fatty acid ethyl ethers in human whole blood by gas chromatography-mass spectrometry.  |  Li, J., et al. 2017. Alcohol. 62: 41-47. PMID: 28755750
  7. Fatty acid ethyl esters: non-oxidative metabolites of ethanol.  |  Laposata, M., et al. 1995. Prostaglandins Leukot Essent Fatty Acids. 52: 87-91. PMID: 7784463
  8. Purification of fatty acid ethyl esters by solid-phase extraction and high-performance liquid chromatography.  |  Bernhardt, TG., et al. 1996. J Chromatogr B Biomed Appl. 675: 189-96. PMID: 8852705
  9. Ethyl palmitate and ethyl oleate are the predominant fatty acid ethyl esters in the blood after ethanol ingestion and their synthesis is differentially influenced by the extracellular concentrations of their corresponding fatty acids.  |  Dan, L. and Laposata, M. 1997. Alcohol Clin Exp Res. 21: 286-92. PMID: 9113265

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Ethyl Heptadecanoate, 5 g

sc-294551
5 g
$172.00

Ethyl Heptadecanoate, 25 g

sc-294551A
25 g
$520.00