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).
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Ammonium oxalate is 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

It is produced in the body of

kidney stone.[3][4] It is also found in guano
.

Mineralogy

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

Chemistry

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

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

  1. ^ .
  2. ^ a b National Center for Biotechnology Information. PubChem Compound Database; CID 14213 (accessed 15 November 2016).
  3. .
  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. .