Potassium thiocyanate
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Potassium thiocyanate | |
---|---|
Other names | potassium sulfocyanate potassium isothiocyanate potassium thiocyanide |
Identifiers | |
CAS number | [333-20-0] |
RTECS number | XL1925000 |
Properties | |
Molecular formula | KSCN |
Molar mass | 97.18 g/mol |
Appearance | colorless crystals deliquescent |
Density | 1.89 g/cm3, solid |
Melting point |
173 °C |
Boiling point |
500 °C |
Solubility in water | 2170 g/L |
Solubility in other solvents | e.g. ethanol acetone:210 g/L |
Hazards | |
Main hazards | toxic |
R-phrases | 20/21/22-32-52/53 |
S-phrases | 13-61 |
Related compounds | |
Other cations | NaSCN |
Related compounds | Potassium cyanide Potassium cyanate |
Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa) Infobox disclaimer and references |
Potassium thiocyanate is the chemical compound with the molecular formula KSCN. It is an important salt of the thiocyanate anion, one of the pseudohalides. The compound has a low melting point relative to most other inorganic salts.
[edit] Use in chemical synthesis
Aqueous KSCN reacts almost quantitatively with Pb(NO3)2 to give Pb(SCN)2. The lead compound has been used to convert acyl chlorides to the thiocyanates.[1]
KSCN converts ethylene carbonate to ethylenesulfide.[2] For this purpose, the KSCN is first melted under vacuum to remove water. In a related reaction, KSCN converts cyclohexene oxide to the corresponding episulfide.[3]
- C6H10O + KSCN → C6H10S + KOCN
Its the starting product for the synthesis of carbonyl sulfide.
[edit] Other uses
Dilute aqueous KSCN is occasionally used for moderately realistic blood effects in film and theater. It can be painted onto a surface or kept as a colourless solution. When in contact with ferric chloride solution, the product of the reaction is a blood red solution.
[edit] References
- ^ Smith, P. A. S.; Kan, R. O. (1973). "2a-Thiohomophthalimide". Org. Synth.; Coll. Vol. 5: 1051.
- ^ Searles, S.; Lutz, E. F.; Hays, H. R.; Mortensen, H. E. (1973). "Ethylenesulfide". Org. Synth.; Coll. Vol. 5: 562.
- ^ van Tamelen, E. E. (1963). "Cyclohexenesulfide". Org. Synth.; Coll. Vol. 4: 232.