Names | |
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Preferred IUPAC name 2-Imido-1,3-dithiodicarbonic diamide | |
Identifiers | |
CAS Number | |
3D model (JSmol) | |
ChEMBL | |
ChemSpider | |
ECHA InfoCard | 100.007.987 |
EC Number |
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MeSH | 2,4-dithiobiuret |
PubChem CID | |
RTECS number |
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UNII | |
UN number | 2811 |
CompTox Dashboard (EPA) | |
InChI
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SMILES
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Properties | |
Chemical formula | C2H5N3S2 |
Molar mass | 135.20 g·mol |
Appearance | White crystals |
Density | 1.54 g/cm |
log P | −0.415 |
Acidity (pKa) | 11.152 |
Basicity (pKb) | 2.845 |
Hazards | |
GHS labelling: | |
Pictograms | |
Signal word | Danger |
Hazard statements | H300, H310, H330 |
Precautionary statements | P260, P280, P284, P302+P350, P310 |
Related compounds | |
Related compounds | |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). Infobox references |
Dithiobiuret is an organosulfur compound with the formula HN(C(S)NH2)2. It is a colourless solid that is soluble in warm water and polar organic solvents. It is a planar molecule with short C-S and C-N distances (1.69, 1.38 Å, resp.) indicative of multiple C-S and C-N bonding.
The compound can be viewed as the product from the condensation of two molecules of thiourea, but it is prepared by treatment of 2-cyanoguanidine with hydrogen sulfide. The conversion proceeds via guanylthiourea:
- NCNC(NH2) + H2S → HN(C(S)NH2)(C(NH)NH2)
- HN(C(S)NH2)(C(NH)NH2) + H2S → HN(C(S)NH2)2
It is used as a plasticizer, a rubber accelerator, and as an intermediate in pesticide manufacturing. It is extremely toxic; exposure can result in respiratory failure.
See also
References
- Spofford, W. A.; Amma, E. L. (1972). "Crystal and molecular structure of dithiobiuret". Journal of Crystal and Molecular Structure. 2 (4): 151–158. doi:10.1007/BF01275491.
- Dithiobiuret Hazardous Substance Fact Sheet, New Jersey Department of Health and Senior Services
External links
- Williams, KD; Porter, WR; Peterson, RE (1982). "Dithiobiuret metabolism in the rat". Neurotoxicology. 3 (4): 221–31. PMID 6820683.
- Dithiobiuret at www.chemicalbook.com.