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Thiocyanic acid

Thiocyanic acid
Skeletal formula of thiocyanic acid
Skeletal formula of thiocyanic acid with the explicit hydrogen added
Spacefill model of thiocyanic acid
Names
IUPAC name
Nitridosulfanidocarbon
Other names
  • Hydrogen thiocyanate
  • Sulfocyanic acid
  • Sulfocyanide
Identifiers
463-56-9 YesY
3D model (Jmol) Interactive image
3DMet B00344
ChEBI CHEBI:29200 YesY
ChEMBL ChEMBL84336 YesY
ChemSpider 760 YesY
ECHA InfoCard 100.006.672
EC Number 207-337-4
25178
KEGG C01755 N
MeSH thiocyanic+acid
PubChem 781
Properties
CHNS
Molar mass 59.09 g·mol−1
Appearance colorless, oily liquid
Odor pungent
Density 2.04 g/cm3
Melting point 5 °C (41 °F; 278 K)
Miscible
Solubility soluble in ethanol, diethyl ether
log P 0.429
Acidity (pKa) 0.926
Basicity (pKb) 13.071
Hazards
Harmful Xn
R-phrases R20/21/22, R32, R52/53
S-phrases (S2), S13
Related compounds
Related alkanenitriles
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
N  (what is YesYN ?)
Infobox references

Thiocyanic acid is a chemical compound with the formula HSCN which exists as a tautomer with isothiocyanic acid (HNCS). The iso- form tends to dominate with the material being about 95% isothiocyanic acid in the vapor phase.

It is a weak acid, bordering on strong, with a pKa of 1.1 at 20 °C and extrapolated to zero ionic strength.

HSCN is predicted to have a triple bond between carbon and nitrogen. It has been observed spectroscopically but has not been isolated as a pure substance.

The salts and esters of thiocyanic acid are known as thiocyanates. The salts are composed of the thiocyanate ion (SCN) and a suitable metal cation (e.g., potassium thiocyanate, KSCN). The esters of thiocyanic acid have the general structure R–SCN.


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