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IUPAC name Potassium hydrosulfide | |
Other names Potassium bisulfide, Potassium sulfhydrate, potassium hydrogen sulfide | |
Identifiers | |
CAS Number | |
3D model (JSmol) | |
ChemSpider | |
ECHA InfoCard | 100.013.803 |
EC Number |
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PubChem CID | |
UNII | |
CompTox Dashboard (EPA) | |
InChI
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SMILES
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Properties | |
Chemical formula | KSH |
Molar mass | 72.171 g/mol |
Appearance | white solid |
Density | 1.68–1.70 g/cm |
Melting point | 455 °C (851 °F; 728 K) |
Solubility in water | good |
Hazards | |
Occupational safety and health (OHS/OSH): | |
Main hazards | Flammable solid, stench, releases hydrogen sulfide |
NFPA 704 (fire diamond) | 3 2 0 |
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 , 100 kPa). N verify (what is ?) Infobox references |
Potassium hydrosulfide is an inorganic compound with the formula KSH. 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. Aqueous solutions of potassium sulfide consist of a mixture of potassium hydrosulfide and potassium hydroxide.
The structure of the potassium hydrosulfide resembles that of potassium chloride. Their structure is however complicated by the non-spherical symmetry of the SH anions, but these tumble rapidly in the solid.
The addition of sulfur gives dipotassium pentasulfide.
Synthesis
It is prepared by neutralizing aqueous KOH with H2S.
References
- Dittmer, Donald C. (2001). "Potassium Hydrogen Sulfide". In Paquette, L. (ed.). Encyclopedia of Reagents for Organic Synthesis. J. Wiley & Sons, New York. doi:10.1002/047084289X.rp227. ISBN 0471936235.
- Haarmann, F; Jacobs, H.; Roessler, E.; Senker, J. (2002). "Dynamics of Anions and Cations in Hydrogensulfides of Alkali Metals (NaHS, KHS, RbHS): A Proton Nuclear Magnetic Resonance Study". Journal of Chemical Physics. 117 (3): 1269–1276. Bibcode:2002JChPh.117.1269H. doi:10.1063/1.1483860.
- Kurzer, F.; Lawson, A. (1962). "Thiobenzoylthioglycolic Acid". Organic Syntheses. 42: 100. doi:10.15227/orgsyn.042.0100.
- Robert L. Frank and James R. Blegen (1948). "Benzoyl Disulfide". Organic Syntheses. 28: 16. doi:10.15227/orgsyn.028.0016.
Potassium compounds | |
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H, (pseudo)halogens | |
chalcogens | |
pnictogens | |
B, C group | |
transition metals | |
organic |