Tartronic acid

From Wikipedia, the free encyclopedia

This is an old revision of this page, as edited by DePiep (talk | contribs) at 19:12, 28 March 2014 (check and adjust {Chembox} temperatures (fmt references, notes, brackets, numerics) using AWB). The present address (URL) is a permanent link to this revision, which may differ significantly from the current revision.

Tartronic acid
Names
IUPAC name
2-hydroxypropanedioic acid
Other names
tartronic acid,
2-tartronic acid,
hydroxymalonic acid,
2-hydroxymalonic acid,
hydroxypropanedioic acid
Identifiers
3D model (JSmol)
ChEBI
ChemSpider
ECHA InfoCard 100.001.184 Edit this at Wikidata
EC Number
  • 201-301-1
KEGG
  • InChI=1S/C3H4O5/c4-1(2(5)6)3(7)8/h1,4H,(H,5,6)(H,7,8) checkY
    Key: ROBFUDYVXSDBQM-UHFFFAOYSA-N checkY
  • InChI=1/C3H4O5/c4-1(2(5)6)3 (7)8/h1,4H,(H,5,6)(H,7,8)
  • InChI=1/C3H4O5/c4-1(2(5)6)3(7)8/h1,4H,(H,5,6)(H,7,8)
    Key: ROBFUDYVXSDBQM-UHFFFAOYAD
  • O=C(O)C(O)C(=O)O
Properties
C3H4O5
Molar mass 120.06 g/mol
Appearance beige powder
Melting point 159 °C (318 °F; 432 K)
Hazards
NFPA 704 (fire diamond)
NFPA 704 four-colored diamondHealth 2: Intense or continued but not chronic exposure could cause temporary incapacitation or possible residual injury. E.g. chloroformFlammability 0: Will not burn. E.g. waterInstability 0: Normally stable, even under fire exposure conditions, and is not reactive with water. E.g. liquid nitrogenSpecial hazards (white): no code
2
0
0
Related compounds
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 ?)

Tartronic acid or 2-hydroxymalonic acid is a dicarboxylic acid with the structural formula of HOOCCH(OH)COOH.

Its derivative, 2-methyltartronic acid, is isomalic acid.

Uses

Tartronic acids are best known as a reactant in the catalytic oxidation with air to form mesoxalic acid, another type of hydroxydicarboxylic acid.[1]

References

  1. ^ Fordham P., Besson M., Gallezot P. (1997). "Catalytic oxidation with air of tartronic acid to mesoxalic acid on bismuth-promoted platinum". Catal. Lett. 46 (3–4): 195–199(5). doi:10.1023/A:1019082905366. Retrieved 2007-07-06.{{cite journal}}: CS1 maint: multiple names: authors list (link)

External links