Date published: 2026-5-6

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Methyl octacosanoate (CAS 55682-92-3)

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Alternate Names:
Octacosanoic acid methyl ester
CAS Number:
55682-92-3
Molecular Weight:
438.77
Molecular Formula:
C29H58O2
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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Methyl octacosanoate, a long-chain methyl ester, has garnered attention in scientific research for its potential applications across various fields. Its chemical structure, comprising a methyl group attached to a saturated 28-carbon fatty acid chain, offers unique properties conducive to diverse research endeavors. In lipidomics, methyl octacosanoate serves as a model compound for studying the metabolism and biophysical properties of long-chain fatty acids, contributing to a deeper understanding of lipid metabolism in cellular and physiological contexts. Additionally, its use in materials science has been explored, particularly in the synthesis of biocompatible coatings and films for biomedical and industrial applications. Researchers have investigated its role as a lubricant additive, enhancing the lubricating properties of oils and greases in mechanical systems. Furthermore, methyl octacosanoate has found utility in organic synthesis as a versatile building block for the preparation of complex molecules, facilitating the development of novel materials and compounds. Its multifaceted nature makes methyl octacosanoate a valuable tool in scientific research, with applications ranging from lipidomics and materials science to organic synthesis and lubrication technology.


Methyl octacosanoate (CAS 55682-92-3) References

  1. Monoglycerides and fatty acids from Ibervillea sonorae root: isolation and hypoglycemic activity.  |  Hernández-Galicia, E., et al. 2007. Planta Med. 73: 236-40. PMID: 17318782
  2. Chemical constituents with antibacterial activity from Euphorbia sororia.  |  Zhang, WK., et al. 2008. Nat Prod Res. 22: 353-9. PMID: 18322851
  3. Specificity of 1-triacontanol as a plant growth stimulator and inhibition of its effect by other long-chain compounds.  |  Jones, J., et al. 1979. Planta. 144: 277-82. PMID: 24407259
  4. Assessing chemical constituents of Mimosa caesalpiniifolia stem bark: possible bioactive components accountable for the cytotoxic effect of M. caesalpiniifolia on human tumour cell lines.  |  Monção, NB., et al. 2015. Molecules. 20: 4204-24. PMID: 25751783
  5. Synthesis of ω9-tetracosynoic and ω9-octacosynoic acids as entries into tritiated metabolic precursors ofcis-9-tricosene andcis-9-heptacosene in the housefly.  |  George Pomonis, J. and Hakk, H. 1990. Lipids. 25: 821-6. PMID: 27520687
  6. Comparison of three methods for the methylation of aliphatic and aromatic compounds.  |  Lee, H., et al. 2017. Rapid Commun Mass Spectrom. 31: 1633-1640. PMID: 28763166
  7. Identification of very long-chain (>C24) fatty acid methyl esters using gas chromatography coupled to quadrupole/time-of-flight mass spectrometry with atmospheric pressure chemical ionization source.  |  Garlito, B., et al. 2019. Anal Chim Acta. 1051: 103-109. PMID: 30661606
  8. High-Throughput Profiling of Metabolic Phenotypes Using High-Resolution GC-MS.  |  Wase, N., et al. 2022. Methods Mol Biol. 2539: 235-260. PMID: 35895208
  9. Novel brominated phospholipid fatty acids from the Caribbean sponge Petrosia sp.  |  Carballeira, NM. and Shalabi, F. 1993. J Nat Prod. 56: 739-46. PMID: 8326322
  10. The vaporization enthalpies and vapor pressures of fatty acid methyl esters C18, C21 to C23, and C25 to C29 by correlation–gas chromatography.  |  Chickos, et al. 2004. Thermochimica acta. 424.1-2: 111-121.

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Methyl octacosanoate, 250 mg

sc-211888
250 mg
$99.00