Erythorbic acid | |
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(5R)-5-[(1R)-1,2-dihydroxyethyl]-3,4-dihydroxyfuran-2(5H)-one |
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Other names
D-Araboascorbic acid, Erythorbate, Isoascorbic acid, E315 |
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Identifiers | |
CAS number | 89-65-6 |
PubChem | 6981 |
ChemSpider | 16736142 |
UNII | 311332OII1 |
ChEBI | CHEBI:51438 |
Jmol-3D images | Image 1 |
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Properties | |
Molecular formula | C6H8O6 |
Molar mass | 176.13 g/mol |
Density | 0.704 g/cm3 |
Melting point |
164–172 °C (decomposes) |
Acidity (pKa) | 2.1 |
(verify) (what is: / ?) Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa) |
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Infobox references |
Erythorbic acid, formerly known as isoascorbic acid and D-araboascorbic acid, is a stereoisomer of ascorbic acid (vitamin C).[1] It is a vegetable-derived food additive produced from sucrose. It is denoted by E number E315, and is widely used as an antioxidant in processed foods.[2]
Clinical trials have been conducted to investigate aspects of the nutritional value of erythorbic acid. One such trial investigated the effects of erythorbic acid on vitamin C metabolism in young women; no effect on vitamin C uptake or clearance from the body was found.[3] A later study found that erythorbic acid is a potent enhancer of nonheme-iron absorption.[4]
Since the U.S. Food and Drug Administration banned the use of sulfites as a preservative in foods intended to be eaten fresh (such as salad bar ingredients), the use of erythorbic acid as a food preservative has increased. It is also used as a preservative in cured meats and frozen vegetables.[5]