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Ethyl palmitate (CAS 628-97-7)

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Alternate Names:
Ethyl hexadecanoate
Application:
Ethyl palmitate is an ethyl ester of palmitic acid
CAS Number:
628-97-7
Purity:
≥98%
Molecular Weight:
284.48
Molecular Formula:
C18H36O2
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 palmitate, identified by the CAS number 628-97-7, is an ester formed from ethanol and palmitic acid. This chemical is characterized by a fatty acid linked to an ethyl group, which alters both its solubility and volatility compared to its fatty acid counterpart. In research, ethyl palmitate is extensively utilized as a model compound to study esterification reactions, providing insights into the kinetics and mechanisms of ester bond formation and breakdown. It serves as a critical substance in the examination of lipid interactions and behaviors, particularly in the investigation of lipid solubility and diffusion properties in various solvents and environments. The relatively low molecular weight and non-polar nature of ethyl palmitate make it an excellent candidate for studies in organic synthesis and green chemistry, where it is often used as a solvent or as a green alternative to more toxic, traditional organic solvents. Additionally, its properties are exploited in the field of material science, particularly in the development and characterization of bio-based polymers and plastics, where it acts as a plasticizer to improve material flexibility without compromising biodegradability. Ethyl palmitate′s stability and low toxicity also enable its use in environmental science research, particularly in studies related to the biodegradation of esters and their environmental impact.


Ethyl palmitate (CAS 628-97-7) References

  1. Saturated fatty acids, but not unsaturated fatty acids, induce the expression of cyclooxygenase-2 mediated through Toll-like receptor 4.  |  Lee, JY., et al. 2001. J Biol Chem. 276: 16683-9. PMID: 11278967
  2. Palmitoylation of the human prostacyclin receptor. Functional implications of palmitoylation and isoprenylation.  |  Miggin, SM., et al. 2003. J Biol Chem. 278: 6947-58. PMID: 12488443
  3. Testing venous carbohydrate-deficient transferrin or capillary phosphatidylethanol with concurrent ethyl glucuronide and ethyl palmitate hair tests to assess historical and recent alcohol use.  |  Tsanaclis, L., et al. 2021. Drug Test Anal. 13: 203-207. PMID: 33025638
  4. Fatty acid ethyl esters in meconium: A biomarker of fetal alcohol exposure and effect.  |  Cheng, CT., et al. 2021. Exp Biol Med (Maywood). 246: 380-386. PMID: 33210553
  5. Fatty acid ethyl esters in meconium and substance use in adolescence.  |  Min, MO., et al. 2021. Neurotoxicol Teratol. 83: 106946. PMID: 33340653
  6. Ethyl palmitate, an anti-chikungunya virus principle from Sauropus androgynus, a medicinal plant used to alleviate fever in ethnomedicine.  |  Sagna, A., et al. 2023. J Ethnopharmacol. 309: 116366. PMID: 36914036
  7. Ethyl palmitate-induced splenic destruction.  |  Prosnitz, L., et al. 1969. J Reticuloendothel Soc. 6: 487-97. PMID: 5349132
  8. Influence of dietary supplementation with fish on plasma fatty acid composition in coronary heart disease patients.  |  Santos, MJ., et al. 1995. Ann Nutr Metab. 39: 52-62. PMID: 7872656
  9. Caveolin is palmitoylated on multiple cysteine residues. Palmitoylation is not necessary for localization of caveolin to caveolae.  |  Dietzen, DJ., et al. 1995. J Biol Chem. 270: 6838-42. PMID: 7896831
  10. Mutagenesis of palmitoylation sites in endothelial nitric oxide synthase identifies a novel motif for dual acylation and subcellular targeting.  |  Robinson, LJ. and Michel, T. 1995. Proc Natl Acad Sci U S A. 92: 11776-80. PMID: 8524847

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Ethyl palmitate, 5 g

sc-391203
5 g
$35.00

Ethyl palmitate, 25 g

sc-391203A
25 g
$88.00

Ethyl palmitate, 100 g

sc-391203B
100 g
$280.00