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Key Documents

09154

Sigma-Aldrich

L-Xylonic acid lithium salt

≥95.0% (TLC)

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About This Item

Empirical Formula (Hill Notation):
C5H10O6 · xLi+
CAS Number:
Molecular Weight:
166.13 (free acid basis)
UNSPSC Code:
12352106
PubChem Substance ID:
NACRES:
NA.25

Assay

≥95.0% (TLC)

form

solid

optical activity

[α]/D -18±2°, c = 1 in H2O

color

white

storage temp.

2-8°C

SMILES string

OC[C@H](O)[C@@H](O)[C@H](O)C(O)=O

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-/m0/s1

InChI key

QXKAIJAYHKCRRA-NUNKFHFFSA-N

Biochem/physiol Actions

Metabolite of the pentose and glucuronate interconversions and the ascorbate and aldarate metabolism.

Other Notes

To gain a comprehensive understanding of our extensive range of Monosaccharides for your research, we encourage you to visit our Carbohydrates Category page.

Storage Class Code

11 - Combustible Solids

WGK

WGK 3


Certificates of Analysis (COA)

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Rocio García-Villalba et al.
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Analysis of compounds in meteorites revealed a need to simultaneously characterize multiple enantiomers of sugar acids (aldonic acids) present in trace amounts. Analyses by gas chromatography-mass spectrometry demonstrated that all but two of the three-carbon through six-carbon straight-chained sugar acid
Wen Shan Yew et al.
Biochemistry, 45(49), 14582-14597 (2006-12-06)
Many members of the mechanistically diverse enolase superfamily have unknown functions. In this report we use both genome (operon) context and screening of a library of acid sugars to assign the L-fuconate dehydratase (FucD) function to a member of the

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