tert-Butyl glycidyl ether

• Formula: C₇H₁₄O₂
• Molecular weight: 130.1849
• IUPAC Standard InChI: InChI=1S/C7H14O2/c1-7(2,3)9-5-6-4-8-6/h6H,4-5H2,1-3H3 Copy

  
• IUPAC Standard InChIKey: SFJRUJUEMVAZLM-UHFFFAOYSA-N Copy
• CAS Registry Number: 7665-72-7
• 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.
• Other names: (tert-Butoxymethyl)oxirane; t-Butyl glycidyl ether; Oxirane, [(1,1-dimethylethoxy)methyl]-; t-Bge; 1,1-Dimethylethyl glycidyl ether; Propane, 1-tert-butoxy-2,3-epoxy-; ((1,1-Dimethylethoxy)methyl)oxirane; Ageflex TBGE; Glycidyl tert-butyl ether; 2-(tert-Butoxymethyl)oxirane; 2,3-Epoxypropyl-t-butyl ether; Oxirane, 2-((1,1-dimethylethoxy)methyl)-
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• Information on this page:
  • Gas phase thermochemistry data
  • Condensed phase thermochemistry data
  • Phase change data
  • Mass spectrum (electron ionization)
  • References
  • Notes
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Gas phase thermochemistry 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 as indicated in comments:
DRB - Donald R. Burgess, Jr.
ALS - Hussein Y. Afeefy, Joel F. Liebman, and Stephen E. Stein

Condensed phase thermochemistry 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: Hussein Y. Afeefy, Joel F. Liebman, and Stephen E. Stein

Phase change 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: Hussein Y. Afeefy, Joel F. Liebman, and Stephen E. Stein

Mass spectrum (electron ionization)

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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: NIST Mass Spectrometry Data Center, William E. Wallace, director

Spectrum

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Additional Data

References

Go To: Top, Gas phase thermochemistry data, Condensed phase thermochemistry data, Phase change data, Mass spectrum (electron ionization), Notes

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

Slivinsky, Dolidze, et al., 1993
Slivinsky, E.V.; Dolidze, A.V.; Loktev, S.M., Hydroformylation of 2,3- and 2,5-dihydrofurans in the presence of a homogeneous catalytic complex based on dicarbonylrhodium acetylacetonate modified with various phosphites, Neftekhimiya, 1993, 33, 102-113. [all data]

Van-Chin-Syan and Kachurina, 1987
Van-Chin-Syan, Yu.Ya.; Kachurina, N.S., Thermochemical properties of oxirane derivatives, Russ. J. Phys. Chem. (Engl. Transl.), 1987, 61, 622-624. [all data]

Zaikin, Wang, et al., 1975
Zaikin, I.D.; Wang, C-H.; Chuchmarev, S.K., The dissociation energy of the peroxide bond in dialkyl peroxides, Russ. J. Phys. Chem. (Engl. Transl.), 1975, 49, 1818-1819. [all data]

Zaikin, Van-Chin-Syan, et al., 1973
Zaikin, I.D.; Van-Chin-Syan, Yu.Ya.; Chuchmarev, S.K.; Elagin, G.I., Standard heats of formation of certain t-alkyl glycidyl ethers, Russ. J. Phys. Chem. (Engl. Transl.), 1973, 47, 925. [all data]

Zaikin, Van Chin Syan, et al., 1972
Zaikin, I.; Van Chin Syan, Y.Y.; Chuchmarev, S.K.; Elagin, G.I., Normal heats of formation of some epoxy compounds, Izv. Vyssh. Uchebn. Zaved., Khim. Khim. Tekhnol., 1972, 15, 1193-1195. [all data]

Notes

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• Symbols used in this document:
  

  ΔcH°liquid	Enthalpy of combustion of liquid at standard conditions
  ΔfH°gas	Enthalpy of formation of gas at standard conditions
  ΔfH°liquid	Enthalpy of formation of liquid at standard conditions
  ΔvapH°	Enthalpy of vaporization at standard conditions

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