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IUPAC name Sodium 2-(carboxymethyl)-2,4-dihydroxy-4-oxobutanoate | |
Other names sodium dihydrogen 2-hydroxypropane-1,2,3-tricarboxylate | |
Identifiers | |
CAS Number | |
3D model (JSmol) | |
ChEBI | |
ChemSpider | |
ECHA InfoCard | 100.038.834 |
EC Number |
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E number | E331i (antioxidants, ...) |
PubChem CID | |
RTECS number |
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UNII | |
CompTox Dashboard (EPA) | |
InChI
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SMILES
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Properties | |
Chemical formula | C6H7NaO7 |
Molar mass | 214.105 g·mol |
Appearance | white powder hygroscopic |
Odor | odorless |
Melting point | 212 °C (414 °F; 485 K) |
Boiling point | 309.6 °C (589.3 °F; 582.8 K) |
Solubility in water | soluble |
Solubility | negligible in ethanol |
Acidity (pKa) | 3.50–3.80 |
Structure | |
Crystal structure | Monoclinic |
Space group | P21/a (No. 4) |
Formula units (Z) | 4 |
Hazards | |
Lethal dose or concentration (LD, LC): | |
LD50 (median dose) | 5400 mg/kg (mouse, oral) >2000 mg/kg (rat, dermal) |
Safety data sheet (SDS) | Carl Roth |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). N verify (what is ?) Infobox references |
Monosodium citrate, more correctly, sodium dihydrogen citrate (Latin: natrium citricum acidulatum), is an acid salt of citric acid. Disodium citrate and trisodium citrate are also known. It can be prepared by partial neutralisation of citric acid with an aqueous solution of sodium bicarbonate or carbonate. It has a slightly acidic taste.
- NaHCO3 + C6H8O7 → NaC6H7O7 + CO2 + H2O
- Na2CO3 + 2C6H8O7 → 2NaC6H7O7 + CO2 + H2O
It is highly soluble in water and practically insoluble in ethanol. Monosodium citrate is used as an anticoagulant in donated blood. It is used as an alkalinizing agent to prevent kidney stone disease. The crystals form as nearly perfect cubes.
References
- https://pubchem.ncbi.nlm.nih.gov/compound/23662352#section=IUPAC-Name&fullscreen=true
- Glusker, Jenny P.; van der Helm, D.; Love, Warner E.; Dornberg, Marilyn L.; Patterson, A. L. (June 1960). "The State of Ionization of Crystalline Sodium Dihydrogen Citrate1". Journal of the American Chemical Society. 82 (11): 2964–2965. doi:10.1021/ja01496a071. ISSN 0002-7863. Retrieved 22 July 2022.
- ^ "Monosodium Citrate - Jungbunzlauer". www.jungbunzlauer.com. Retrieved 17 July 2022.
- Clinical Hematology: Theory and Procedures, Mary Louise Turgeon
- PubChem. "Monosodium citrate". pubchem.ncbi.nlm.nih.gov. Retrieved 2021-08-02.
- Hitchcock, David I. (March 1946). "Sodium Hydrogen Citrates". Journal of the American Chemical Society. 68 (3): 524–525. doi:10.1021/ja01207a507. ISSN 0002-7863. PMID 21015754. Retrieved 22 July 2022.
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