Potassium hydrosulfide

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Potassium hydrosulfide
Sodium-hydrosulfide-LT-xtal-1991-CM-3D-balls.png
Names
IUPAC name
Potassium hydrosulfide
Other names
Potassium bisulfide, Potassium sulfhydrate, potassium hydrogen sulfide
Identifiers
1310-61-8 YesY
ChemSpider 92246 N
EC Number 215-182-9
Jmol 3D model Interactive image
PubChem 102109
  • InChI=1S/K.H2S/h;1H2/q+1;/p-1 N
    Key: ZOCLAPYLSUCOGI-UHFFFAOYSA-M N
  • InChI=1/K.H2S/h;1H2/q+1;/p-1
    Key: ZOCLAPYLSUCOGI-REWHXWOFAJ
  • [SH-].[K+]
Properties
KHS[1]
Molar mass 72.171 g/mol
Appearance white solid
Density 1.68–1.70 g/cm3
Melting point 455 °C (851 °F; 728 K)
good
Vapor pressure {{{value}}}
Related compounds
Other anions
Potassium hydroxide
Other cations
Sodium hydrosulfide
Related compounds
potassium sulfide
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
N verify (what is YesYN ?)
Infobox references

Potassium hydrosulfide is the inorganic compound with the formula KHS. This colourless salt consists of the cation K+ and the bisulfide anion [SH]. It is the product of the half-neutralization of hydrogen sulfide with potassium hydroxide. The compound is used in the synthesis of some organosulfur compounds.[2] It is prepared by neutralizing aqueous KOH with H2S.[3] Aqueous solutions of potassium sulfide consist of a mixture of potassium hydrosulfide and potassium hydroxide.

The structure of the potassium hydrosulfide resembles that for potassium chloride. Their structure is however complicated by the non-spherical symmetry of the SH anions, but these tumble rapidly in the solid high temperatures.[4]

Addition of sulfur gives dipotassium pentasulfide.

Synthesis

Potassium hydrosulfide is synthesized by the reaction between a solution of potassium sulfide with excess hydrogen sulfide.

References

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  2. Dittmer, D. C. "Potassium Hydrogen Sulfide" in Encyclopedia of Reagents for Organic Synthesis (Ed: L. Paquette) 2004, J. Wiley & Sons, New York. doi: 10.1002/047084289.
  3. Kurzer, F. Lawson, A. "Thiobenzoylthioglycolic Acid" Organic Syntheses, Collected Volume 5, p.1046 (1973). [1]
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