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Sigma-Aldrich

D-Xylonsäure Lithiumsalz

≥95.0% (TLC)

Synonym(e):

Lithium-D-xylonat

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About This Item

Empirische Formel (Hill-System):
C5H10O6 · xLi+
CAS-Nummer:
526-91-0
Molekulargewicht:
166.13 (free acid basis)
UNSPSC-Code:
12352201
PubChem Substanz-ID:
329765134
NACRES:
NA.25

Qualitätsniveau

100

Assay

≥95.0% (TLC)

Form

powder or crystals

Optische Aktivität

[α]/D 18±2° in H2O

Farbe

white to off-white

Lagertemp.

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

InChIKey

QXKAIJAYHKCRRA-FLRLBIABSA-N

Verwandte Kategorien

Biochem./physiol. Wirkung

Metabolite of pentose and glucuronate interconversions

Sonstige Hinweise

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

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Analysenzertifikate (COA)

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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.
Bioresource technology, 133, 555-562 (2013-03-05)
D-xylonic acid is one of the top 30 most desirable chemicals to be derived from biomass sugars identified by the US Department of Energy, being applicable as a non-food substitute for D-gluconic acid and as a platform chemical. We engineered
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)
Huaiwei Liu et al.
Bioresource technology, 115, 244-248 (2011-09-16)
An engineered Escherichia coli was constructed to produce D-xylonic acid, one of the top 30 high-value chemicals identified by US Department of Energy. The native pathway for D-xylose catabolism in E. coli W3110 was blocked by disrupting xylose isomerase (XI)
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