Dithiobiuret
| Names | |
|---|---|
| Preferred IUPAC name 2-Imido-1,3-dithiodicarbonic diamide | |
| Identifiers | |
| 3D model (JSmol) | |
| ChEMBL | |
| ChemSpider | |
| ECHA InfoCard | 100.007.987 | 
| EC Number | 
 | 
| MeSH | 2,4-dithiobiuret | 
| PubChem CID | |
| RTECS number | 
 | 
| UNII | |
| UN number | 2811 | 
| CompTox Dashboard (EPA) | |
| 
 | |
| 
 | |
| Properties | |
| C2H5N3S2 | |
| Molar mass | 135.20 g·mol−1 | 
| Appearance | White crystals | 
| Density | 1.54 g/cm3 | 
| log P | −0.415 | 
| Acidity (pKa) | 11.152 | 
| Basicity (pKb) | 2.845 | 
| Hazards | |
| GHS labelling: | |
| Danger | |
| H300, H310, H330 | |
| 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 [77 °F], 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.