Thiocarbohydrazide

In today's world, Thiocarbohydrazide is a topic that has captured the attention of people everywhere. From its impact on society to its implications on daily life, Thiocarbohydrazide is a topic that we cannot ignore. As we delve into this article, we will explore the different facets of Thiocarbohydrazide and its influence on different aspects of life. From its origins to its evolution over time, we will dive into a detailed analysis that will allow us to better understand the importance of Thiocarbohydrazide in today's world. Join us on this journey to discover everything you need to know about Thiocarbohydrazide.

Thiocarbohydrazide
Names
Preferred IUPAC name
Hydrazinecarbothiohydrazide
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 Edit this at Wikidata
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)
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa).

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