Misplaced Pages

Thiocarbohydrazide

Article snapshot taken from Wikipedia with creative commons attribution-sharealike license. Give it a read and then ask your questions in the chat. We can research this topic together.
Thiocarbohydrazide
Names
Preferred IUPAC name Hydrazinecarbothiohydrazide
Other names 1,3-Diamino-2-thiourea; Thiocarbazide; Thiocarbonic dihydrazide; Thiocarbonyldihydrazide; Carbonothioic dihydrazide; TCh; Thiocarbonohydrazide
Identifiers
CAS Number
3D model (JSmol)
ChemSpider
ECHA InfoCard 100.017.064 Edit this at Wikidata
PubChem CID
UNII
CompTox Dashboard (EPA)
InChI
  • InChI=1S/CH6N4S/c2-4-1(6)5-3/h2-3H2,(H2,4,5,6)Key: LJTFFORYSFGNCT-UHFFFAOYSA-N
  • InChI=1/CH6N4S/c2-4-1(6)5-3/h2-3H2,(H2,4,5,6)Key: LJTFFORYSFGNCT-UHFFFAOYAM
SMILES
  • C(=S)(NN)NN
Properties
Chemical formula CH6N4S
Molar mass 106.15 g·mol
Melting point 171 to 174 °C (340 to 345 °F; 444 to 447 K) (decomposes)
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). Infobox references
Chemical compound

Thiocarbohydrazide is a toxic compound made by the reaction of carbon disulfide with hydrazine (hydrazinolysis). It is used in the silver proteinate specific staining of carbohydrates in electron microscopy.

References

  1. International Union of Pure and Applied Chemistry (2014). Nomenclature of Organic Chemistry: IUPAC Recommendations and Preferred Names 2013. The Royal Society of Chemistry. p. 878. doi:10.1039/9781849733069. ISBN 978-0-85404-182-4.
  2. Thiocarbohydrazide at Sigma-Aldrich
Categories: