1,2,4-Trithiolane, 3,5-bis(1-methylethyl)-

• Formula: C₈H₁₆S₃
• Molecular weight: 208.408
• IUPAC Standard InChI: InChI=1S/C8H16S3/c1-5(2)7-9-8(6(3)4)11-10-7/h5-8H,1-4H3 Copy

  
• IUPAC Standard InChIKey: QCTAPVCDZUSECS-UHFFFAOYSA-N Copy
• CAS Registry Number: 54934-99-5
• Chemical structure:
  This structure is also available as a 2d Mol file
• Species with the same structure:
  • 1,2,4-Trithiolane, 3,5-bis-(1-methylethyl), #1
• Other names: 3,5-Diisopropyl-1,2,4-trithiolane; 1,2,4-Trithiolane, 3,5-bis-(1-methylethyl), #2; 3,5-Di-isopropyl-[1,2,4]trithiolane, stereoisomer 2
• Information on this page:
  • Gas Chromatography
  • References
  • Notes
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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, custom temperature program

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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.

Kawai, Ishida, et al., 1991
Kawai, T.; Ishida, Y.; Kakiuchi, H.; Ikeda, N.; Higashida, T.; Nakamura, S., Flavor components of dried squid, J. Agric. Food Chem., 1991, 39, 4, 770-777, https://doi.org/10.1021/jf00004a031 . [all data]

Vernin, Metzger, et al., 1993
Vernin, G.; Metzger, J.; Sultan, A.A.M.; El-Shafei, A.K.; Párkányi, C., Heterocyclic compounds in model systems for the Maillard reaction. Reactions of aldehydes with ammonium sulfide in the presence or absence of acetoin, Am. Chem. Soc. Symp. Ser., 1993, 528, 36-55. [all data]

Notes

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