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| Names | |
|---|---|
| IUPAC name
 Potassium hydrogen sulfite  | |
| Other names
 Potassium bisulfite, potassium bisulphite, monopotassium salt, monopotassium sulfite, potassium hydrosulfite  | |
| Identifiers | |
3D model (JSmol)  | 
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| ChemSpider | |
| ECHA InfoCard | 100.028.973 | 
| EC Number | 
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| E number | E228 (preservatives) | 
PubChem CID  | 
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| UNII | |
CompTox Dashboard (EPA)  | 
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| Properties | |
| KHSO3 | |
| Molar mass | 120.1561 g/mol | 
| Appearance | White crystalline powder | 
| Odor | SO2-like | 
| Melting point | 190 °C (374 °F; 463 K) (decomposes) | 
| 49 g/100 mL (20 °C)  115 g/100 mL (100 °C)  | |
| Solubility | Insoluble in alcohol | 
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). 
Infobox references  | |
Potassium bisulfite (or potassium hydrogen sulfite) is a chemical mixture with the approximate chemical formula KHSO3. Potassium bisulfite in fact is not a real compound,[1] but a mixture of salts that dissolve in water to give solutions composed of potassium ions and bisulfite ions. It is a white solid with an odor of sulfur dioxide. Attempts to crystallize potassium bisulfite yield potassium metabisulfite, K2S2O5.[2]
Potassium bisulfite is used as a sterilising agent in the production of alcoholic beverages.[3] This additive is classified as E number E228 under the current EU-approved food additive legislation.[4]
Production
It is made by the reaction of sulfur dioxide and potassium carbonate. The sulfur dioxide is passed through a solution of the potassium carbonate until no more carbon dioxide is evolved. The solution is concentrated.
See also
References
- ↑ Tudela, David; Jenkins, H. Donald B. (2003). "New Methods to Estimate Lattice Energies: Application to the Relative Stabilities of Bisulfite (HSO3−) and Metabisulfite (S2O52-) Salts". Journal of Chemical Education. 80 (12): 1482. Bibcode:2003JChEd..80.1482T. doi:10.1021/ed080p1482.
 - ↑ Johnstone, H. F. (1946). "Sulfites and Pyrosulfites of the Alkali Metals". Inorganic Syntheses. Inorganic Syntheses. Vol. 2. pp. 162–167. doi:10.1002/9780470132333.ch49. ISBN 9780470132333.
 - ↑ Barberá, José Jiménez; Metzger, Adolf; Wolf, Manfred (2000). "Sulfites, Thiosulfates, and Dithionitesl Chemistry". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a25_477. ISBN 978-3527306732.
 - ↑ "Approved additives and E numbers". Food Standards Agency. Retrieved 2020-04-07.
 

