This colorless deliquescent salt is one of the main sources of the thiocyanate anion.
Each Na+ center is surrounded by three sulfur and three nitrogen ligands provided by the triatomic thiocyanate anion.
Sodium thiocyanate is employed to convert alkyl halides into the corresponding alkylthiocyanates.
[4] Protonation of sodium thiocyanate affords isothiocyanic acid, S=C=NH (pKa = −1.28).
[5] This species is generated in situ from sodium thiocyanate; it adds to organic amines to afford derivatives of thiourea.