Xylonic acid

d-Xylonic acid
Names
	IUPAC name (2R,3S,4R)-2,3,4,5-tetrahydroxypentanoic acid
	Other names Xylonate
Identifiers
CAS Number	17828-56-7 (d/l) ; 526-91-0 (d) ; 4172-44-5 (l>) ;
3D model (JSmol)	Interactive image;
ChEBI	CHEBI:48093 (d); CHEBI:48092 (l);
ChemSpider	5034782 ;
PubChem CID	6602431;
	InChI 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 Key: QXKAIJAYHKCRRA-FLRLBIABSA-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;
	SMILES C([C@H]([C@@H]([C@H](C(=O)O)O)O)O)O;
Properties
Chemical formula	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).
	verify (what is ?)
	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

PubChem. "L-Xylonic acid". pubchem.ncbi.nlm.nih.gov. Retrieved 2019-06-02.
"D-Xylonic acid | C5H10O6 | ChemSpider". www.chemspider.com. Retrieved 2019-06-02.
"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.

[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.