61786
D-Glyceric acid sodium salt
≥95.0% (TLC)
Synonym(s):
(R)-2,3-Dihydroxypropanoic acid sodium salt, Sodium D-glycerate
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About This Item
Empirical Formula (Hill Notation):
C3H6O4 · xNa+
CAS Number:
Molecular Weight:
106.08 (free acid basis)
MDL number:
UNSPSC Code:
12352201
NACRES:
NA.25
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Quality Level
Assay
≥95.0% (TLC)
form
powder or crystals
optical activity
[α]/D 18.5±3.0°, c = 1 in water
color
white
SMILES string
O[C@H](CO)C(=O)O
InChI
1S/C3H6O4/c4-1-2(5)3(6)7/h2,4-5H,1H2,(H,6,7)/t2-/m1/s1
InChI key
RBNPOMFGQQGHHO-UWTATZPHSA-N
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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
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Theresa Kouril et al.
The FEBS journal, 280(4), 1126-1138 (2013-01-03)
Sulfolobus solfataricus P2 is a thermoacidophilic archaeon that metabolizes glucose and galactose via an unusual branched Entner-Doudoroff (ED) pathway, which is characterized by a non-phosphorylative (np) and a semi-phosphorylative (sp) branch. However, so far the physiological significance of the two
J D Goldberg et al.
Journal of molecular biology, 236(4), 1123-1140 (1994-03-04)
D-Glycerate dehydrogenase (GDH) catalyzes the NADH-linked reduction of hydroxypyruvate to D-glycerate. GDH is a member of a family of NAD-dependent dehydrogenases that is characterized by a specificity for the D-isomer of the hydroxyacid substrate. The crystal structure of the apoenzyme
S K Wadman et al.
Clinica chimica acta; international journal of clinical chemistry, 71(3), 477-484 (1976-09-20)
A patient is described with glyceric acidemia and glyceric aciduria. The main clinical problems in infancy were severe metabolic acidosis and failure to thrive. The patient needs permanent treatment with bicarbonate. Hyperglycinemia, as described in the first case discovered elsewhere
E Van Schaftingen
FEBS letters, 243(2), 127-131 (1989-01-30)
D-Glycerate kinase was measured in human livers thanks to a new, sensitive radiochemical assay. The enzyme was extremely unstable in extracts prepared in water, but was partly stabilized in a homogenization mixture containing inorganic phosphate, D-glycerate and EGTA. When extracted
Jörn Oliver Sass et al.
Human mutation, 31(12), 1280-1285 (2010-10-16)
D-glyceric aciduria is a rare inborn error of serine and fructose metabolism that was first described in 1974. Most affected individuals have presented with neurological symptoms. The molecular basis of D-glyceric aciduria is largely unknown; possible causes that have been
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