Oxirane, ethyl-

• Formula: C₄H₈O
• Molecular weight: 72.1057
• IUPAC Standard InChI: InChI=1S/C4H8O/c1-2-4-3-5-4/h4H,2-3H2,1H3 Copy

  
• IUPAC Standard InChIKey: RBACIKXCRWGCBB-UHFFFAOYSA-N Copy
• CAS Registry Number: 106-88-7
• Chemical structure:
  This structure is also available as a 2d Mol file or as a computed 3d SD file
  The 3d structure may be viewed using Java or Javascript.
• Species with the same structure:
  • Oxirane, ethyl-
• Other names: Butane, 1,2-epoxy-; α-Butylene oxide; n-Butene-1,2-oxide; But-1-ene oxide; Ethylethylene oxide; Ethyloxirane; 1-Butene oxide; 1-Butylene oxide; 1,2-Butene oxide; 1,2-Butylene oxide; 1,2-Epoxybutane; 2-Ethyloxirane; Butylene oxide; Ethylene oxide, ethyl-; NCI-C55527; 1,2-Monoepoxybutane; Epoxybutane; (.+/-.)-2-Ethyloxirane; DL-1,2-Epoxybutane; NSC 24240; Oxirane, 2-ethyl-
• Information on this page:
  • Gas phase ion energetics data
  • References
  • Notes
• Other data available:
  • Gas phase thermochemistry data
  • Condensed phase thermochemistry data
  • Phase change data
  • IR Spectrum
  • Mass spectrum (electron ionization)
  • Gas Chromatography
• Data at other public NIST sites:
  • Gas Phase Kinetics Database
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Gas phase ion energetics data

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Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.

Data compiled by: Sharon G. Lias, Rhoda D. Levin, and Sherif A. Kafafi

View reactions leading to C₄H₈O⁺ (ion structure unspecified)

Ionization energy determinations

References

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Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.

McAlduff and Houk, 1977
McAlduff, E.J.; Houk, K.N., Photoelectron spectra of substituted oxiranes and thiiranes. Substituent effects on ionization potentials involving σ orbitals, Can. J. Chem., 1977, 55, 318. [all data]

Notes

Go To: Top, Gas phase ion energetics data, References

• Data from NIST Standard Reference Database 69: NIST Chemistry WebBook
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