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Methanedithiol information


Methanedithiol
Names
Preferred IUPAC name
Methanedithiol
Other names
Dimercaptomethane
Identifiers
CAS Number
  • 6725-64-0
3D model (JSmol)
  • Interactive image
ChemSpider
  • 122421
ECHA InfoCard 100.166.842 Edit this at Wikidata
PubChem CID
  • 138818
UNII
  • LSC543N4PH
CompTox Dashboard (EPA)
  • DTXSID50217580 Edit this at Wikidata
InChI
  • InChI=1S/CH4S2/c2-1-3/h2-3H,1H2
    Key: INBDPOJZYZJUDA-UHFFFAOYSA-N
SMILES
  • SCS
Properties
Chemical formula
CH4S2
Molar mass 80.16 g·mol−1
Appearance Colorless liquid
Boiling point 58 °C (136 °F; 331 K)
Refractive index (nD)
1.581
Hazards
GHS labelling:
Pictograms
GHS02: Flammable
Signal word
Warning
Hazard statements
H226
Precautionary statements
P210, P233, P240, P241, P242, P243, P280, P303+P361+P353, P370+P378, P403+P235, P501
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references

Methanedithiol is an organosulfur compound with the formula H2C(SH)2. It forms when formaldehyde is treated with hydrogen sulfide under pressure. The reaction competes with formation of trithiane. The compound forms a solid dibenzoate upon treatment with benzoic anhydride.[1]

  1. ^ Cairns, T. L.; Evans, G. L.; Larchar, A. W.; McKusick, B. C. (1952). "gem-Dithiols". Journal of the American Chemical Society. 74 (16): 3982–9. doi:10.1021/ja01136a004.

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Methanedithiol

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Methanedithiol is an organosulfur compound with the formula H2C(SH)2. It forms when formaldehyde is treated with hydrogen sulfide under pressure. The reaction...

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Dithiol

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stability contrasts with the rarity of geminal diols. Examples include methanedithiol, ethane-1,1-dithiol, and cyclohexane-1,1-dithiol. Upon heating, gem-dithiols...

Word Count : 524

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