Date published: 2025-11-21

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1,2-Epoxyoctadecane (CAS 7390-81-0)

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CAS Number:
7390-81-0
Molecular Weight:
268.48
Molecular Formula:
C18H36O
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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1,2-Epoxyoctadecane, also referred to as 1,2-epoxy-octadecane, is an organic compound classified as an epoxide within its chemical family. On exploring the versatile applications of 1,2-epoxyoctadecane across various scientific fields, including organic synthesis, and polymerization. Its broad utility has been observed in the synthesis of polymers, organic compounds, and biocompatible materials. Mechanistically, 1,2-epoxyoctadecane functions as an epoxide, enabling it to act as a nucleophile by attacking electrophilic centers within organic molecules. This reactivity initiates an epoxidation reaction, leading to the formation of a stable three-membered ring structure, facilitated by resonance stabilization. 1,2-epoxyoctadecane can act as a leaving group, allowing displacement by nucleophiles in epoxide opening reactions.


1,2-Epoxyoctadecane (CAS 7390-81-0) References

  1. Stellan Hjertén's contribution to the development of monolithic stationary phases.  |  Svec, F. 2008. Electrophoresis. 29: 1593-603. PMID: 18383033
  2. Core-shell diamond as a support for solid-phase extraction and high-performance liquid chromatography.  |  Saini, G., et al. 2010. Anal Chem. 82: 4448-56. PMID: 20446670
  3. Determination of essential oil composition from Osmanthus fragrans tea by GC-MS combined with a chemometric resolution method.  |  Hu, CD., et al. 2010. Molecules. 15: 3683-93. PMID: 20657507
  4. Pellicular particles with spherical carbon cores and porous nanodiamond/polymer shells for reversed-phase HPLC.  |  Wiest, LA., et al. 2011. Anal Chem. 83: 5488-501. PMID: 21688788
  5. Facile preparation of a stable and functionalizable hybrid monolith via ring-opening polymerization for capillary liquid chromatography.  |  Lin, H., et al. 2013. J Chromatogr A. 1301: 131-8. PMID: 23806359
  6. Systematic evaluation of the physicochemical properties and the volatile flavors of yak meat during chilled and controlled freezing-point storage.  |  Sun, S., et al. 2020. J Food Sci Technol. 57: 1351-1361. PMID: 32180631
  7. Study the lipidoid nanoparticle mediated genome editing protein delivery using 3D intestinal tissue model.  |  Yang, T., et al. 2021. Bioact Mater. 6: 3671-3677. PMID: 33898871
  8. Fecal Metabolomics Reveals Distinct Profiles of Kidney Transplant Recipients and Healthy Controls.  |  Kouidhi, S., et al. 2021. Diagnostics (Basel). 11: PMID: 33946812
  9. Effect of Feeding Barley, Corn, and a Barley/Corn Blend on Beef Composition and End-Product Palatability.  |  Barragán-Hernández, W., et al. 2021. Foods. 10: PMID: 33946945
  10. Chemical Emissions From Heated Vitamin E Acetate-Insights to Respiratory Risks From Electronic Cigarette Liquid Oil Diluents Used in the Aerosolization of Δ9-THC-Containing Products.  |  LeBouf, RF., et al. 2021. Front Public Health. 9: 765168. PMID: 35127617
  11. The Improvement of Sensory and Bioactive Properties of Yogurt with the Introduction of Tartary Buckwheat.  |  Ye, Y., et al. 2022. Foods. 11: PMID: 35741972
  12. Chemical Composition and In Vitro Antioxidant Activity of Sida rhombifolia L. Volatile Organic Compounds.  |  Xu, Z., et al. 2022. Molecules. 27: PMID: 36296660
  13. Fertility regulatory potential of Persicaria hydropiper (L.) Delarbre methanolic root extract in female albino mice: An insight into the phytochemicals present and role of the extract in contraception.  |  Bairagi, J., et al. 2022. Saudi Pharm J. 30: 1623-1638. PMID: 36465841

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

1,2-Epoxyoctadecane, 25 g

sc-273535
25 g
$52.00