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Names | |
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IUPAC name Dipotassium 2,3-dihydroxybutanedioate | |
Other names Dipotassium tartrate; Argol; E336 | |
Identifiers | |
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3D model (JSmol) | |
ChemSpider |
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ECHA InfoCard | 100.005.180![]() |
UNII |
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Properties | |
C4H4K2O6 | |
Molar mass | 226.268 g/mol |
Appearance | colorless, slightly opaque crystals |
Density | 1.984 g/cm3 |
Solubility | insoluble inalcohol |
Refractive index (nD) | 1.550 |
Structure | |
monoclinic | |
Except where otherwise noted, data are given for materials in theirstandard state (at 25 °C [77 °F], 100 kPa). |
Potassium tartrate,dipotassium tartrate orargol has formula K2C4H4O6. It is thepotassiumsalt oftartaric acid. It is often confused withpotassium bitartrate, also known as cream of tartar. As afood additive, it shares theE numberE336 with potassium bitartrate.[1]
Potassium bitartrate, also referred to as potassium acid tartrate or cream of tartar,[2] is the potassium acid salt of l-( + )-tartaric acid. It is obtained as a byproduct of wine manufacture during the fermentation process. Approved by the FDA as a direct food substance, potassium bitartrate is used as an additive, stabilizer, pH control agent, antimicrobial agent, processing aid, or thickener in various food products. Potassium bitartrate has a long history of medical use as a laxative administered as a rectal suppository and is an approved third-class OTC drug in Japan.
Potassium bitartrate was one of active ingredients in Phexxi, a non-hormonal contraceptive agent that was approved by the FDA in May 2020.[3]
Potassium tartrate is produced by the reaction oftartaric acid with potassium sodium tartrate (rochelle salt), andpotassium sulfate, followed by filtration, purification, precipitation and drying.
Tartar emetic is produced when potassium tartrate is heated withantimony trioxide. Tartar emetic causes intense nausea, prostration and vomiting by irritating the gastrointestinal mucosa.https://go.drugbank.com/drugs/DB11107