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Potassium thiocyanate

From Wikipedia, the free encyclopedia
Potassium thiocyanate
Names
Other names
Potassium sulfocyanate
Potassium isothiocyanate (tautomeric form)
Potassium thiocyanide
Potassium rhodanide
Identifiers
3D model (JSmol)
3594799
ChEBI
ChemSpider
ECHA InfoCard100.005.792Edit this at Wikidata
EC Number
  • 206-370-1
21362
RTECS number
  • XL1925000
UNII
  • InChI=1S/CHNS.K/c2-1-3;/h3H;/q;+1/p-1 checkY
    Key: ZNNZYHKDIALBAK-UHFFFAOYSA-M checkY
  • InChI=1/CHNS.K/c2-1-3;/h3H;/q;+1/p-1
    Key: ZNNZYHKDIALBAK-REWHXWOFAT
  • C(#N)[S-].[K+]
Properties
KSCN
Molar mass97.181 g mol−1
AppearanceColorlessdeliquescent crystals
OdorOdorless
Density1.886 g/cm3
Melting point173.2 °C (343.8 °F; 446.3 K)
Boiling point500 °C (932 °F; 773 K) (decomposes)
177 g/100 mL (0 °C)
217 g/100 mL (20 °C)
Solubilityacetone: 21.0 g/100 mL
ethanol: soluble[citation needed]
−48.0·10−6 cm3/mol
Hazards
GHS labelling:
GHS05: CorrosiveGHS07: Exclamation mark
Warning
H302,H312,H318,H319,H332,H412
P261,P264,P270,P271,P273,P280,P301+P312,P302+P352,P304+P312,P304+P340,P305+P351+P338,P310,P312,P322,P330,P337+P313,P363,P501
NFPA 704 (fire diamond)
Lethal dose or concentration (LD, LC):
854 mg/kg (oral, rat)[1]
Safety data sheet (SDS)ICSC 1088
Related compounds
Otheranions
Potassium cyanate
Potassium cyanide
Othercations
Sodium thiocyanate
Ammonium thiocyanate
Except where otherwise noted, data are given for materials in theirstandard state (at 25 °C [77 °F], 100 kPa).
☒N verify (what is checkY☒N ?)
Chemical compound

Potassium thiocyanate is thechemical compound with the molecular formula KSCN. It is an important salt of thethiocyanateanion, one of thepseudohalides. The compound has a low melting point relative to most other inorganic salts.

Uses

[edit]

Chemical synthesis

[edit]

Aqueous KSCN reacts almost quantitatively withPb(NO3)2 to give Pb(SCN)2, which has been used to convertacyl chlorides to isothiocyanates.[2]

KSCN convertsethylene carbonate toethylene sulfide.[3] For this purpose, the KSCN is first melted under vacuum to remove water. In a related reaction, KSCN convertscyclohexene oxide to the correspondingepisulfide andKOCN.[4]

C6H10O + KSCN → C6H10S + KOCN

KSCN is also the starting product for the synthesis ofcarbonyl sulfide.

Special effects

[edit]

Dilute aqueous KSCN is occasionally used for moderately realistic blood effects in film and theatre. It can be painted onto a surface or kept as a colorless solution. When in contact withferric chloride solution (or other solutions containingFe3+), the product of the reaction is a solution with a blood red colour, due to the formation of thethiocyanatoironcomplex ion. Thus this chemical is often used to create the effect of 'stigmata'. Because both solutions are colorless, they can be placed separately on each hand. When the hands are brought into contact, the solutions react and the effect looks remarkably likestigmata.[citation needed]

Laboratory

[edit]

The reaction with Fe3+ mentioned above is used as atest for Fe3+ ions in thelaboratory.

Law enforcement

[edit]

Approximatecocaine purity can be determined using 1 mL 2% cupric sulphate pentahydrate in dilute HCl, 1 mL 2% potassium thiocyanate and 2 mL ofchloroform. The shade of brown shown by the chloroform is proportional to the cocaine content. This test is not cross sensitive to heroin, methamphetamine, benzocaine, procaine and a number of other drugs but other chemicals could cause false positives.[5]

References

[edit]
  1. ^"Potassium thiocyanate [NF]".chem.sis.nlm.nih.gov.Archived from the original on 20 April 2018. Retrieved19 April 2018.
  2. ^Smith, P. A. S.; Kan, R. O. (1973)."2a-Thiohomophthalimide".Organic Syntheses;Collected Volumes, vol. 5, p. 1051.
  3. ^Searles, S.; Lutz, E. F.; Hays, H. R.; Mortensen, H. E. (1973)."Ethylenesulfide".Organic Syntheses;Collected Volumes, vol. 5, p. 562.
  4. ^van Tamelen, E. E. (1963)."Cyclohexenesulfide".Organic Syntheses;Collected Volumes, vol. 4, p. 232.
  5. ^Travnikoff B (1 April 1983). "Semiquantitative screening test for cocaine".Analytical Chemistry.55 (4):795–796.doi:10.1021/ac00255a048.ISSN 0003-2700.
H, (pseudo)halogens
chalcogens
pnictogens
B, C group
transition metals
organic
Salts and covalent derivatives of thethiocyanate ion

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