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73671

D-Xylonic acid lithium salt

≥95.0% (TLC)

Synonym(s):

Lithium D-xylonate

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Pack SizeSKUAvailabilityPrice
100 mg
Please contact Customer Service for Availability
$380.00
500 mg
Please contact Customer Service for Availability
$1,500.00

About This Item

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

$380.00


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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.

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This Item
798497276473097
assay

≥95.0% (TLC)

assay

95% (TLC)

assay

≥95.0% (HPLC)

assay

≥70% (qNMR), ≥95% (TLC)

Quality Level

100

Quality Level

100

Quality Level

100

Quality Level

100

form

powder or crystals

form

powder or crystals

form

powder or crystals

form

powder or crystals

storage temp.

2-8°C

storage temp.

2-8°C

storage temp.

−20°C

storage temp.

2-8°C

color

white to off-white

color

-

color

-

color

white to off-white

optical activity

[α]/D 18±2° in H2O

optical activity

-

optical activity

-

optical activity

[α]/D 15±2°, c = 1 in H2O


Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable



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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
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
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)



Global Trade Item Number

SKUGTIN
73671-10MG04061832385655
73671-500MG04061832385662
73671-100MG04061832385648
73671-5G04061832385679

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