Thiocarbohydrazide

Last updated
Thiocarbohydrazide
Thiocarbohydrazide.svg
Names
Preferred IUPAC name
Hydrazinecarbothiohydrazide [1]
Other names
1,3-Diamino-2-thiourea; Thiocarbazide; Thiocarbonic dihydrazide; Thiocarbonyldihydrazide; Carbonothioic dihydrazide; TCh; Thiocarbonohydrazide
Identifiers
3D model (JSmol)
ChemSpider
ECHA InfoCard 100.017.064 OOjs UI icon edit-ltr-progressive.svg
PubChem CID
UNII
  • 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
  • C(=S)(NN)NN
Properties
CH6N4S
Molar mass 106.15 g·mol−1
Melting point 171 to 174 °C (340 to 345 °F; 444 to 447 K)(decomposes) [2]
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references

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.

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Organic chemistry Subdiscipline of chemistry

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Organometallic chemistry Study of chemical compounds containing at least one bond between a carbon atom of an organic compound and a metal

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Carbazide

In chemistry, a carbazide is a functional group with the general formula RNH-NH(C=O)NH-NHR. They can be derived from the condensation of carbonic acid with a hydrazine. Carbohydrazide is the simplest carbazide, with another common carbazide being diphenylcarbazide, which is used as an analytical reagent.

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