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Potassium thiocyanate





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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.

Potassium thiocyanate
Names
Other names

Potassium sulfocyanate
Potassium isothiocyanate (tautomeric form)
Potassium thiocyanide
Potassium rhodanide

Identifiers

CAS Number

3D model (JSmol)

Beilstein Reference

3594799
ChEBI
ChemSpider
ECHA InfoCard 100.005.792 Edit this at Wikidata
EC Number
  • 206-370-1

Gmelin Reference

21362

PubChem CID

RTECS number
  • XL1925000
UNII

CompTox Dashboard (EPA)

  • 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

Chemical formula

KSCN
Molar mass 97.181 g mol−1
Appearance Colorless deliquescent crystals
Odor Odorless
Density 1.886 g/cm3
Melting point 173.2 °C (343.8 °F; 446.3 K)
Boiling point 500 °C (932 °F; 773 K) (decomposes)

Solubility in water

177 g/100 mL (0 °C)
217 g/100 mL (20 °C)
Solubility acetone: 21.0 g/100 mL
ethanol: soluble

Magnetic susceptibility (χ)

−48.0·10−6cm3/mol
Hazards
GHS labelling:

Pictograms

GHS05: CorrosiveGHS07: Exclamation mark

Signal word

Warning

Hazard statements

H302, H312, H318, H319, H332, H412

Precautionary statements

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)
NFPA 704 four-colored diamondHealth 2: Intense or continued but not chronic exposure could cause temporary incapacitation or possible residual injury. E.g. chloroformFlammability 0: Will not burn. E.g. waterInstability 0: Normally stable, even under fire exposure conditions, and is not reactive with water. E.g. liquid nitrogenSpecial hazards (white): no code
2
0
0
Lethal dose or concentration (LD, LC):

LD50 (median dose)

854 mg/kg (oral, rat)[1]
Safety data sheet (SDS) ICSC 1088
Related compounds

Other anions

Potassium cyanate
Potassium cyanide

Other cations

Sodium thiocyanate
Ammonium thiocyanate

Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

☒N verify (what is checkY☒N ?)

Infobox references

Uses

edit

Chemical synthesis

edit

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

KSCN converts ethylene carbonatetoethylene sulfide.[3] 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 and KOCN. [4]

 

KSCN is also the starting product for the synthesis of carbonyl 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 with ferric chloride solution (or other solutions containing Fe3+), the product of the reaction is a solution with a blood red colour, due to the formation of the thiocyanatoiron complex 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 like stigmata.[citation needed]

Laboratory

edit

The reaction with Fe Fe3+ mentioned above is used as a test for Fe3+ in the laboratory.

Law enforcement

edit

Approximate cocaine purity can be determined using 1 mL 2% cupric sulphate pentahydrate in dilute HCl, 1 mL 2% potassium thiocyanate and 2 mL of chloroform. 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. Retrieved 19 April 2018.
  • ^ Smith, P. A. S.; Kan, R. O. (1973). "2a-Thiohomophthalimide". Organic Syntheses; Collected Volumes, vol. 5, p. 1051.
  • ^ Searles, S.; Lutz, E. F.; Hays, H. R.; Mortensen, H. E. (1973). "Ethylenesulfide". Organic Syntheses; Collected Volumes, vol. 5, p. 562.
  • ^ van Tamelen, E. E. (1963). "Cyclohexenesulfide". Organic Syntheses; Collected Volumes, vol. 4, p. 232.
  • ^ Travnikoff B (1 April 1983). "Semiquantitative screening test for cocaine". Analytical Chemistry. 55 (4): 795–796. doi:10.1021/ac00255a048. ISSN 0003-2700.

  • Retrieved from "https://en.wikipedia.org/w/index.php?title=Potassium_thiocyanate&oldid=1208452069"
     



    Last edited on 17 February 2024, at 15:42  





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    This page was last edited on 17 February 2024, at 15:42 (UTC).

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