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(2R,3S)-2,3-Dihydroxybutyric acid sodium salt hydrate

≥97.0% (GC)

Synonym(s):

(2R,3S)-2,3-Dihydroxybutanoic acid sodium salt hydrate, 4-Deoxy-L-threonic acid sodium salt hydrate

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About This Item

Empirical Formula (Hill Notation):
C4H8O4 · xNa+ · yH2O
Molecular Weight:
120.10 (anhydrous free acid basis)
UNSPSC Code:
12352200
PubChem Substance ID:
NACRES:
NA.24

assay

≥97.0% (GC)

optical activity

[α]/D 27±3°, c = 0.5 in 0.1 M NaOH

format

neat

storage temp.

2-8°C

Biochem/physiol Actions

(2R,3S)-2,3-Dihydroxybutyric acid is the enantiomer of (2S,3R)- 2,3-dihydroxybutanoic acid, which is a normally occurring carboxylic acid in humans. Metabolic profiling of urinary organic acids from patients with Type 1 diabetes mellitus (juvenile-onset) have revealed significantly elevated levels of this metabolite. The normal urinary constituent (2S,3R)-2,3-dihydroxybutanoic acid was found to diminish in urine incubated with E. coli.

Storage Class

13 - Non Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable


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Bipolar disorder (BD) is a complex debilitating mental disorder that is often misdiagnosed as major depressive disorder (MDD). Therefore, a large percentage of BD subjects are incorrectly treated with antidepressants in clinical practice. To address this challenge, objective laboratory-based tests
K Maeda et al.
Journal of chromatography, 345(1), 11-18 (1985-11-29)
For rapid identification of Escherichia coli, changes of urinary metabolites incubated with E. coli were investigated by gas chromatography--mass spectrometry. Hydroquinone and uracil were detected and the normal urinary constituent 4-deoxythreonic acid was found to diminish in urine incubated with
M Tuchman et al.
Journal of chromatographic science, 22(5), 198-202 (1984-05-01)
Gas chromatographic retention indices (methylene units) are reported for 101 urinary organic acids as their trimethylsilyl and oximated trimethylsilyl derivatives on a 5% phenylmethyl silicone fused silica capillary column. Using anion exchange chromatography, organic acids were extracted from urines of

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