Names | |
---|---|
IUPAC name
2,3-Dihydroxybutanedioic acid calcium salt
| |
Identifiers | |
3D model (JSmol)
|
|
ChemSpider | |
ECHA InfoCard | 100.019.656 |
EC Number |
|
E number | E354 (antioxidants, ...) |
PubChem CID
|
|
UNII |
|
CompTox Dashboard (EPA)
|
|
| |
| |
Properties | |
CaC4H4O6 | |
Molar mass | 190.16484 g/mol (anhydrous) 260.21 g/mol (tetrahydrate) |
Appearance | hygroscopic white powder or colorless crystals |
Density | 1.817 g/cm3 (tetrahydrate) |
Melting point | tetrahydrate decomposes at 160 °C anhydrous decomposes at 650 °C |
0.037 g/100 ml (0 °C) 0.2 g/100 ml (85 °C) | |
Structure | |
d or l rhombic dl triclinic | |
Hazards | |
Safety data sheet (SDS) | Calcium tartrate |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
|
Calcium tartrate, exactly calcium L-tartrate, is a byproduct of the wine industry, prepared from wine fermentation dregs.[1][2][3] It is the calcium salt of L-tartaric acid, an acid most commonly found in grapes.[4] Its solubility decreases with lower temperature, which results in the forming of whitish (in red wine often reddish) crystalline clusters as it precipitates. As E number E354, it finds use as a food preservative and acidity regulator. Like tartaric acid, calcium tartrate has two asymmetric carbons, hence it has two chiral isomers and a non-chiral isomer (meso-form). Most calcium tartrate of biological origin is the chiral levorotatory (–) isomer.