Potassium azide

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Potassium azide
KN3viewCropped.tif
Names
IUPAC name
Potassium azide
Identifiers
20762-60-1 YesY
Jmol 3D model Interactive image
PubChem 10290740
  • InChI=1S/K.N3/c;1-3-2/q+1;-1
    Key: TZLVRPLSVNESQC-UHFFFAOYSA-N
  • [N-]=[N+]=[N-].[K+]
Properties
KN
3
Molar mass 81.1184 g/mol
Appearance Colorless crystals[1]
Density 2.038 g/cm3
[1]
Melting point 350 °C (662 °F; 623 K) (in vacuum)[1]
Boiling point decomposes
41.4 g/100 mL (0 °C)
50.8 g/100 mL (20 °C)
105.7 g/100 mL (100 °C)
Solubility soluble in ethanol
insoluble in ether
Thermochemistry
-1.7 kJ/mol
Vapor pressure {{{value}}}
Related compounds
Other cations
Sodium azide, copper(II) azide, lead(II) azide, silver azide
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
YesY verify (what is YesYN ?)
Infobox references

Potassium azide is the inorganic compound having the formula KN
3
. It is a white, water-soluble salt. It is used as a reagent in the laboratory.

It has been found to act as a nitrification inhibitor in soil.[2]

Structure

KN3, RbN3, CsN3, and TlN3 adopt the same structures. They crystallize in a tetragonal habit.[3] The azide is bound to eight cations in an eclipsed orientation. The cations are bound to eight terminal N centers.[4]

File:AzideCoordinationCropped.tif
Coordination sphere of azide in K,Rb,Cs,TlN3.

Synthesis and reactions

KN3 is prepared by treating potassium carbonate with hydrazoic acid, which is generated in situ.[5] In contrast, the analogous sodium azide is prepared (industrially) by the "Wislicenus process," which proceeds via the reaction sodium amide with nitrous oxide.[6]

Upon heating or upon irradiation with ultraviolet light, it decomposes into potassium metal and nitrogen gas.[7] The decomposition temperatures of the alkali metal azides are: NaN3 (275 °C), KN3 (355 °C), RbN3 (395 °C), CsN3 (390 °C).[8]

Health hazards

Like sodium azide, potassium azide is very toxic. The MAK[disambiguation needed] value for the related sodium azide is 0.07 ppm. The toxicity of azides arise from their ability to inhibit cytochrome c oxidase.[6]

References

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  4. Ulrich Müller "Verfeinerung der Kristallstrukturen von KN3, RbN3, CsN3 und TIN3" Zeitschrift für anorganische und allgemeine Chemie 1972, Volume 392, 159–166. doi:10.1002/zaac.19723920207
  5. P. W. Schenk "Alkali Azides from Carbonates" in Handbook of Preparative Inorganic Chemistry, 2nd Ed. Edited by G. Brauer, Academic Press, 1963, NY. Vol. 1. p. 475.
  6. 6.0 6.1 Horst H. Jobelius, Hans-Dieter Scharff "Hydrazoic Acid and Azides" in Ullmann's Encyclopedia of Industrial Chemistry, 2005, Wiley-VCH, Weinheim. doi:10.1002/14356007.a13_193
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  8. E. Dönges "Alkali Metals" in Handbook of Preparative Inorganic Chemistry, 2nd Ed. Edited by G. Brauer, Academic Press, 1963, NY. Vol. 1. p. 475.