Date published: 2025-10-16

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Methyl oleate (CAS 112-62-9)

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Alternate Names:
Methyl cis-9-octadecenoate; Oleic acid methyl ester
Application:
Methyl oleate is used as a chromatographic reference standard in biochemical research
CAS Number:
112-62-9
Molecular Weight:
296.49
Molecular Formula:
C19H36O2
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 oleate, an ester derived from the monounsaturated fatty acid oleic acid found in vegetable oils, is a colorless, odorless, and viscous liquid. In scientific research, methyl oleate boasts a diverse range of applications. It serves as a vital building block for synthesizing various compounds, particularly fatty acid derivatives, facilitating investigations into the biochemical implications of oleic acid. Furthermore, methyl oleate enables the study of how dietary fatty acids impact metabolism.


Methyl oleate (CAS 112-62-9) References

  1. Methyl oleate modulates LIP2 expression in the lipolytic yeast Yarrowia lipolytica.  |  Fickers, P., et al. 2005. Biotechnol Lett. 27: 1751-4. PMID: 16314965
  2. Mechanistic features of isomerizing alkoxycarbonylation of methyl oleate.  |  Roesle, P., et al. 2012. J Am Chem Soc. 134: 17696-703. PMID: 23072478
  3. Experimental study of the oxidation of methyl oleate in a jet-stirred reactor.  |  Bax, S., et al. 2010. Combust Flame. 157: 1220-1229. PMID: 23710077
  4. Methyl oleate deoxygenation for production of diesel fuel aliphatic hydrocarbons over Pd/SBA-15 catalysts.  |  Lee, SP. and Ramli, A. 2013. Chem Cent J. 7: 149. PMID: 24011181
  5. Methyl oleate as matrix simulacrum for the simultaneous determination of metals in biodiesel samples by flame atomic emission spectroscopy.  |  Cerai Ferreira, C., et al. 2015. Talanta. 138: 8-14. PMID: 25863364
  6. Methyl oleate-capped upconverting nanocrystals: a simple and general ligand exchange strategy to render nanocrystals dispersible in aqueous and organic medium.  |  Meesaragandla, B., et al. 2015. Langmuir. 31: 5521-8. PMID: 25902373
  7. Raman spectroscopy of solid-phase n-dodecane and methyl oleate under high pressure.  |  Yamawaki, H. 2020. Spectrochim Acta A Mol Biomol Spectrosc. 227: 117756. PMID: 31707027
  8. New Lipidyl-Cyclodextrins Obtained by Ring Opening of Methyl Oleate Epoxide Using Ball Milling.  |  Oliva, E., et al. 2020. Biomolecules. 10: PMID: 32093153
  9. Effects of methyl oleate and microparticle-enhanced cultivation on echinocandin B fermentation titer.  |  Niu, K., et al. 2020. Bioprocess Biosyst Eng. 43: 2009-2015. PMID: 32557175
  10. In vitro and in vivo efficacy of methyl oleate and palmitic acid against ESBL producing MDR Escherichia coli and Klebsiella pneumoniae.  |  Padmini, N., et al. 2020. Microb Pathog. 148: 104446. PMID: 32810555
  11. MOF-derived zirconia-supported Keggin heteropoly acid nanoporous hybrids as a reusable catalyst for methyl oleate production.  |  Zhang, Q., et al. 2021. RSC Adv. 11: 8117-8123. PMID: 35423329
  12. Dehydrocyclization-cracking of methyl oleate by Pt catalysts supported on a ZnZSM-5-Al2O3 hierarchical composite.  |  Ishihara, A., et al. 2021. RSC Adv. 11: 19864-19873. PMID: 35479253
  13. Investigation of the enhancement for Echinocandin B fermentation with methyl oleate from transcription level.  |  Niu, K., et al. 2023. Bioprocess Biosyst Eng. 46: 1045-1052. PMID: 37253987

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Methyl oleate, 1 g

sc-215362
1 g
$53.00

Methyl oleate, 5 g

sc-215362A
5 g
$184.00

Methyl oleate, 1 kg

sc-215362B
1 kg
$3060.00