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| Names | |
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| IUPAC name
Sodium (2R)-2-[(1S)-1,2-dihydroxyethyl]-4-hydroxy-5-oxo-2H-furan-3-olate | |
| Other names
Sodascorbate; Monosodium ascorbate; E301 | |
| Identifiers | |
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3D model (JSmol) |
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| ChEBI | |
| ChEMBL | |
| ECHA InfoCard | 100.004.661 
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| EC Number |
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| E number | E301 (antioxidants, ...) |
| KEGG |
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PubChem CID |
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| RTECS number |
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| UNII | |
CompTox Dashboard (EPA) |
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| Properties | |
| C6H7NaO6 | |
| Molar mass | 198.106 g·mol−1 |
| Appearance | minute white to yellow crystals |
| Odor | odorless |
| Density | 1.66 g/cm3 |
| Melting point | 218 °C (424 °F; 491 K) (decomposes) |
| 62 g/100 mL (25 °C) 78 g/100 mL (75 °C) | |
| Solubility | very slightly soluble in alcohol insoluble in chloroform, ether |
| Hazards | |
| NFPA 704 (fire diamond) | |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
Sodium ascorbate is one of a number of mineral salts of ascorbic acid (vitamin C). The molecular formula of this chemical compound is C6H7NaO6. As the sodium salt of ascorbic acid, it is known as a mineral ascorbate. It has not been demonstrated to be more bioavailable than any other form of vitamin C supplement.[2]
Sodium ascorbate normally provides 131 mg of sodium per 1,000 mg of ascorbic acid (1,000 mg of sodium ascorbate contains 889 mg of ascorbic acid and 111 mg of sodium).
As a food additive, it has the E number E301 and is used as an antioxidant and an acidity regulator. It is approved for use as a food additive in the EU,[3] USA,[4] Australia, and New Zealand.[5]
Inin vitro studies, sodium ascorbate has been found to produce cytotoxic effects in various malignant cell lines, which include melanoma cells that are particularly susceptible.[6][7]
Sodium ascorbate is produced by dissolving ascorbic acid in water and adding an equivalent amount of sodium bicarbonate in water. After cessation of effervescence, the sodium ascorbate is precipitated by the addition of isopropanol.
