1,2,4-Trithiolane, 3,3,5,5-tetramethyl-

• Formula: C₆H₁₂S₃
• Molecular weight: 180.354
• IUPAC Standard InChI: InChI=1S/C6H12S3/c1-5(2)7-6(3,4)9-8-5/h1-4H3 Copy

  
• IUPAC Standard InChIKey: XFOWPRWOLKTTSD-UHFFFAOYSA-N Copy
• CAS Registry Number: 38348-31-1
• Chemical structure:
  This structure is also available as a 2d Mol file or as a computed 3d SD file
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• Other names: 3,3,5,5-Tetramethyl-1,2,4-trithiolane; 1,2,4-Trithiolane, tetramethyl-
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• Information on this page:
  • Gas phase ion energetics data
  • Mass spectrum (electron ionization)
  • Gas Chromatography
  • References
  • Notes
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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 as indicated in comments:
LLK - Sharon G. Lias, Rhoda D. Levin, and Sherif A. Kafafi

Ionization energy determinations

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

Gas Chromatography

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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

Normal alkane RI, non-polar column, temperature ramp

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Normal alkane RI, polar column, temperature ramp

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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.

Guimon, Guimon, et al., 1976
Guimon, M.F.; Guimon, C.; Metras, F.; Pfister-Guillouzo, G., Analyse conformationnelle de trithiolannes-1,2,4, Can. J. Chem., 1976, 54, 146. [all data]

Guimon, Guimon, et al., 1975
Guimon, M.-F.; Guimon, C.; Pfister-Guillouzo, G., Application of photoelectron spectroscopy to conformational analysis of 1,2,4-trithiolanes, Tetrahedron Lett., 1975, 7, 441. [all data]

Kubec, Velísek, et al., 1997
Kubec, R.; Velísek, J.; Dolezal, M.; Kubelka, V., Sulfur-containing volatiles arising by thermal degradation of alliin and deoxyalliin, J. Agric. Food Chem., 1997, 45, 9, 3580-3585, https://doi.org/10.1021/jf970071q . [all data]

Notes

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