d-Xylonic acid
Names
IUPAC name
(2R,3S,4R)-2,3,4,5-tetrahydroxypentanoic acid
Other names
Xylonate
Identifiers
3D model (JSmol)
ChEBI
ChemSpider
UNII
  • 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).
☒N verify (what is checkY☒N ?)
Infobox references

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.

References

  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.


This article is issued from Wikipedia. The text is licensed under Creative Commons - Attribution - Sharealike. Additional terms may apply for the media files.