Methanedithiol
Appearance
Names | |
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Other names
Dimercaptomethane
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Identifiers | |
3D model (JSmol)
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ChemSpider | |
ECHA InfoCard | 100.166.842 |
PubChem CID
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UNII | |
CompTox Dashboard (EPA)
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Properties | |
CH4S2 | |
Molar mass | 80.16 g·mol−1 |
Appearance | Colorless liquid |
Boiling point | 58 °C (136 °F; 331 K) |
Refractive index (nD)
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1.581 |
Hazards | |
GHS labelling: | |
Warning | |
H226 | |
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).
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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 competes with formation of trithiane. The compound forms a solid dibenzoate upon treatment with benzoic anhydride.[1]
References
- ^ "gem-Dithiols". Journal of the American Chemical Society. 74: 3982–9. 1952. doi:10.1021/ja01136a004.
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