Methanedithiol

Methanedithiol
Names
	Other names Dimercaptomethane
Identifiers
CAS Number	6725-64-0;
3D model (JSmol)	Interactive image;
ChemSpider	122421;
ECHA InfoCard	100.166.842
PubChem CID	138818;
UNII	LSC543N4PH;
CompTox Dashboard (EPA)	DTXSID50217580 ;
	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 pictograms
GHS Signal word	Warning
GHS hazard statements	H226
GHS precautionary statements	P210, P233, P240, P241, P242, P243, P280, P303+361+353, P370+378, P403+235, 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: 3982–9. doi:10.1021/ja01136a004.CS1 maint: uses authors parameter (link)

This article is issued from Wikipedia. The text is licensed under Creative Commons - Attribution - Sharealike. Additional terms may apply for the media files.

[1] Cairns, T. L.; Evans, G. L.; Larchar, A. W.; McKusick, B. C. (1952). "gem-Dithiols". Journal of the American Chemical Society. 74: 3982–9. doi:10.1021/ja01136a004.CS1 maint: uses authors parameter (link)