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00033

Sigma-Aldrich

D-Arabinonic acid sodium salt

≥98.0% (TLC)

Sinônimo(s):

D-Arabonic acid sodium salt, Sodium D-arabinonate

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About This Item

Fórmula empírica (Notação de Hill):
C5H9NaO6
Número CAS:
109175-66-8
Peso molecular:
188.11
Código UNSPSC:
12352201
ID de substância PubChem:
329746992
NACRES:
NA.25

Ensaio

≥98.0% (TLC)

forma

powder

técnica(s)

thin layer chromatography (TLC): suitable

temperatura de armazenamento

2-8°C

cadeia de caracteres SMILES

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

InChI

1S/C5H10O6.Na/c6-1-2(7)3(8)4(9)5(10)11;/h2-4,6-9H,1H2,(H,10,11);/q;+1/p-1/t2-,3-,4+;/m1./s1

chave InChI

IDBPBTCQINMQJK-PSRPMNHMSA-M

Ações bioquímicas/fisiológicas

Metabolite of the D-arabinose pathway

Código de classe de armazenamento

13 - Non Combustible Solids

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

Not applicable

Ponto de fulgor (°C)

Not applicable

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Ying-Ping Gai et al.
Plant, cell & environment, 37(6), 1474-1490 (2013-12-18)
To analyse the molecular mechanisms of phytoplasma pathogenicity, the comprehensive metabolomic changes of mulberry leaf and phloem sap in response to phytoplasma infection were examined using gas chromatography-mass spectrometry. The metabolic profiles obtained revealed that the metabolite compositions of leaf
B Lu et al.
Electrophoresis, 17(2), 325-332 (1996-02-01)
A rapid and sensitive method for the analysis of sugars was developed by capillary zone electrophoresis (CZE) with indirect UV detection. A mixture of nine mono- and oligosaccharides was separated in about 20 minutes on a fused silica capillary in
Oxidation of D-glucose with oxygen in alkaline methanol-water mixtures: a convenient method of producing crystalline sodium D-arabinonate
Vuorinen, T., et al.
Starch, 43, 194-198 (1991)
Osao Adachi et al.
Bioscience, biotechnology, and biochemistry, 75(9), 1801-1806 (2011-09-08)
In our previous study, a new microbial reaction yielding 4-keto-D-arabonate from 2,5-diketo-D-gluconate was identified with Gluconacetobacter liquefaciens RCTMR 10. It appeared that decarboxylation and dehydrogenation took place together in the reaction. To analyze the nature of the reaction, investigations were
George Cooper et al.
Journal of chromatography. A, 1216(40), 6838-6843 (2009-09-01)
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
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