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Ammonium oxalate

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Ammonium oxalate
Names
IUPAC name
Ammonium oxalate
Systematic IUPAC name
Ammonium ethanedioate
Other names
Diammonium oxalate
Identifiers
3D model (JSmol)
ChEBI
ChemSpider
ECHA InfoCard 100.012.912 Edit this at Wikidata
UNII
  • InChI=1S/C2H2O4.2H3N/c3-1(4)2(5)6;;/h(H,3,4)(H,5,6);2*1H3 checkY
    Key: VBIXEXWLHSRNKB-UHFFFAOYSA-N checkY
  • InChI=1S/C2H2O4.2H3N/c3-1(4)2(5)6;;/h(H,3,4)(H,5,6);2*1H3
  • [O-]C(=O)C([O-])=O.[NH4 ].[NH4 ]
Properties
[NH4]2C2O4
Molar mass 124.096 g·mol−1
Appearance Colorless or white crystalline solid
Density 1.5 g/cm3[1]
Melting point 70 C (158 F, 343.15 K)
5.20 g/(100 ml) (25 °C)[1]
Hazards
GHS labelling:
H302, H312, H319
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
☒N verify (what is checkY☒N ?)

Ammonium oxalate is a chemical compound with the chemical formula [NH4]2C2O4. Its formula is often written as (NH4)2C2O4 or (COONH4)2. It is an ammonium salt of oxalic acid. It consists of ammonium cations ([NH4] ) and oxalate anions (C2O2−4). The structure of ammonium oxalate is ([NH4] )2[C2O4]2−. Ammonium oxalate sometimes comes as a monohydrate ([NH4]2C2O4·H2O). It is a colorless or white salt under standard conditions and is odorless and non-volatile. It occurs in many plants and vegetables.

Vertebrate

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It is produced in the body of vertebrates by metabolism of glyoxylic acid or ascorbic acid. It is not metabolized but excreted in the urine.[2] It is a constituent of some types of kidney stone.[3][4] It is also found in guano.

Mineralogy

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Oxammite is a natural mineral form of ammonium oxalate. This mineral is extremely rare. It is an organic mineral derived from guano.[5]

Chemistry

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Ammonium oxalate is used as an analytical reagent and general reducing agent.[2] It and other oxalates are used as anticoagulants, to preserve blood outside the body.[citation needed]

Earth sciences

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Acid ammonium oxalate (ammonium oxalate acidified to pH 3 with oxalic acid) is commonly employed in soil chemical analysis to extract iron and aluminium from poorly-crystalline minerals (such as ferrihydrite), iron(II)-bearing minerals (such as magnetite) and organic matter.[6][page needed]

References

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  1. ^ a b John Rumble (June 18, 2018). CRC Handbook of Chemistry and Physics (99th ed.). CRC Press. pp. 4–41. ISBN 978-1138561632.
  2. ^ a b National Center for Biotechnology Information. PubChem Compound Database; CID 14213 (accessed 15 November 2016).
  3. ^ The International Pharmacopoeia, p.1292, Volume 1, World Health Organization, 2006 ISBN 92-4-156301-X.
  4. ^ N G Coley, "The collateral sciences in the work of Golding Bird (1814–1854)", Medical History, iss.4, vol.13, October 1969, pp.372.
  5. ^ "Home". mindat.org.
  6. ^ Rayment, George; Lyons, David (2011). Soil Chemical Methods - Australasia. CSIRO Publishing. ISBN 9780643101364.