|  | |
| Names | |
|---|---|
| Preferred IUPAC name Methanedithiol | |
| Other names Dimercaptomethane | |
| Identifiers | |
| 3D model (JSmol) | |
| ChemSpider | |
| ECHA InfoCard | 100.166.842 | 
| PubChem CID | |
| UNII | |
| CompTox Dashboard (EPA) | |
| 
 | |
| 
 | |
| Properties | |
| 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: | |
|  | |
| 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). 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]
References
- ↑ 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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