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73671

Sigma-Aldrich

D-Xylonic acid lithium salt

≥95.0% (TLC)

Synonym(s):

Lithium D-xylonate

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About This Item

Empirical Formula (Hill Notation):
C5H10O6 · xLi+
CAS Number:
Molecular Weight:
166.13 (free acid basis)
UNSPSC Code:
12352201
PubChem Substance ID:
NACRES:
NA.25

Quality Level

Assay

≥95.0% (TLC)

form

powder or crystals

optical activity

[α]/D 18±2° in H2O

color

white to off-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-/m1/s1

InChI key

QXKAIJAYHKCRRA-FLRLBIABSA-N

Biochem/physiol Actions

Metabolite of pentose and glucuronate interconversions

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

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable


Certificates of Analysis (COA)

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Wei Niu et al.
Journal of the American Chemical Society, 125(43), 12998-12999 (2003-10-23)
The lack of a route to precursor 1,2,4-butanetriol that is amenable to large-scale synthesis has impeded substitution of 1,2,4-butanetriol trinitrate for nitroglycerin. To identify an alternative to the current commercial synthesis of racemic d,l-1,2,4-butanetriol involving NaBH4 reduction of esterified d,l-malic
Note on D-xylonate utilization by ascomycetous and basidiomycetous yeasts.
Van Der Walt, J. P. and Steyn, R. L.
Systematic and Applied Microbiology, 13, 192-193 (1990)
Olga Gorte et al.
Biotechnology for biofuels, 13(1), 181-181 (2020-12-10)
Biotechnologically produced microbial lipids are of interest as potential alternatives for crude and plant oils. Their lipid profile is similar to plant oils and can therefore be a substitute for the production of biofuels, additives for food and cosmetics industry
Yvonne Nygård et al.
Metabolic engineering, 25, 238-247 (2014-07-30)
D-xylonate is a potential platform chemical which can be produced by engineered Saccharomyces cerevisiae strains. In order to address production constraints in more detail, we analysed the role of lactone ring opening in single cells and populations. Both D-xylono-γ-lactone and
Mervi Toivari et al.
Metabolic engineering, 14(4), 427-436 (2012-06-20)
An NAD(+)-dependent D-xylose dehydrogenase, XylB, from Caulobacter crescentus was expressed in Saccharomyces cerevisiae, resulting in production of 17 ± 2 g D-xylonate l(-1) at 0.23 gl(-1)h(-1) from 23 g D-xylose l(-1) (with glucose and ethanol as co-substrates). D-Xylonate titre and

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