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Xylonic acid

Summary

Xylonic acid is a sugar acid that can be obtained by oxidation of the hemiacetal/aldehyde group of xylose.[1][2][3] The C-2 epimer is known as lyxonic acid.

d-Xylonic acid
Names
IUPAC name
(2R,3S,4R)-2,3,4,5-tetrahydroxypentanoic acid
Other names
Xylonate
Identifiers
  • 17828-56-7 (d/l) checkY
  • 526-91-0 (d) ☒N
  • 4172-44-5 (l>) ☒N
3D model (JSmol)
  • Interactive image
ChEBI
  • CHEBI:48093 (d)
  • CHEBI:48092 (l)
ChemSpider
  • 5034782 ☒N
  • 6602431
UNII
  • OCI0V55QO1 checkY
  • InChI=1S/C5H10O6/c6-1-2(7)3(8)4(9)5(10)11/h2-4,6-9H,1H2,(H,10,11)/t2-,3+,4-/m1/s1 ☒N
    Key: QXKAIJAYHKCRRA-FLRLBIABSA-N ☒N
  • InChI=1/C5H10O6/c6-1-2(7)3(8)4(9)5(10)11/h2-4,6-9H,1H2,(H,10,11)/t2-,3+,4-/m1/s1
    Key: QXKAIJAYHKCRRA-FLRLBIABBX
  • C([C@H]([C@@H]([C@H](C(=O)O)O)O)O)O
Properties
C
5H
10O
6
Molar mass 166.13 g/mol
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Infobox references

References edit

  1. ^ PubChem. "L-Xylonic acid". pubchem.ncbi.nlm.nih.gov. Retrieved 2019-06-02.
  2. ^ "D-Xylonic acid | C5H10O6 | ChemSpider". www.chemspider.com. Retrieved 2019-06-02.
  3. ^ "XYLONIC ACID | Sigma-Aldrich". www.sigmaaldrich.com. Retrieved 2019-06-02.