Thiocyanuric acid
| |
| Identifiers | |
|---|---|
PubChem CID
|
|
| Properties | |
| C3H3N3S3 | |
| Molar mass | 177.26 g·mol−1 |
| Appearance | yellow solid |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
| |
Thiocyanuric acid is the organosulfur compound with the formula (HNC=S)3. It is analogous to cyanuric acid]] ((HNC=O)3). Cyanuric acid is white whereas thiocyanuric acid is yellow. It can also be viewed as a trimeric thioamide. It is a planar molecular as determined by X-ray crystallography.[1]
The compound is mildly acidic, with pKa's of 5.7, 8.4, and 11.4.[2] Various salts of (HNC=S)−3 have been characterized.[3]
A modern synthesis begins with cyanuric chloride and a source of hydrosulfide.[2]
References
[edit]- ^ Brito, Iván; Albanez, Joselyn; Bolte, Michael (2010). "Trithiacyanuric acid: A second triclinic polymorph". Acta Crystallographica Section e Structure Reports Online. 66 (9): o2382–o2383. Bibcode:2010AcCrE..66o2382B. doi:10.1107/S1600536810033234. PMC 3007918. PMID 21588719.
- ^ a b Henke, Kevin R.; Hutchison, Aaron R.; Krepps, Matthew K.; Parkin, Sean; Atwood, David A. (2001). "Chemistry of 2,4,6-Trimercapto-1,3,5-triazine (TMT): Acid Dissociation Constants and Group 2 Complexes". Inorganic Chemistry. 40 (17): 4443–4447. doi:10.1021/ic0103188. PMID 11487353.
- ^ Dean, Philip A. W.; Jennings, Michael; Houle, Teena M.; Craig, Donald C.; Dance, Ian G.; Hook, James M.; Scudder, Marcia L. (2004). "Crystal packing in tetraphenylphosphonium salts of trithiocyanuric acid and its methanol solvate". CrystEngComm. 6 (88): 543. doi:10.1039/b413145b.