All Photos(1)
Synonym(s):
(S)-2,3-Dihydroxypropanoic acid sodium salt, Sodium L-glycerate
Empirical Formula (Hill Notation):
C3H6O4 · xNa+
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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 H2O
color
white
InChI
1S/C3H6O4/c4-1-2(5)3(6)7/h2,4-5H,1H2,(H,6,7)/t2-/m0/s1
InChI key
RBNPOMFGQQGHHO-REOHCLBHSA-N
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Related Categories
Biochem/physiol Actions
L-Glyceric aciduria is a well known indicator for primary hyperoxaluria type II (MIM ID 260000).
Other Notes
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wgk_germany
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
Certificates of Analysis (COA)
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Identification and location of L-glycerate, an unusual acyl substituent in gellan gum.
Kuo, M.S. and Mort, A.J.
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Nephrolithiasis associated with inborn metabolic diseases is a very rare condition with some common characteristics: early onset of symptoms, family history, associated tubular impairment, bilateral, multiple and recurrent stones, and association with nephrocalcinosis. The prognosis of such diseases may lead
C J Danpure et al.
Journal of inherited metabolic disease, 12(4), 403-414 (1989-01-01)
This paper concerns an enzymological investigation into a putative feline analogue of the human autosomal recessive disease primary hyperoxaluria type 2. The hepatic activities of D-glycerate dehydrogenase, using both D-glycerate and hydroxypyruvate as substrates, and glyoxylate reductase, which are the
Eduardo Salido et al.
Biochimica et biophysica acta, 1822(9), 1453-1464 (2012-03-27)
Glyoxylate detoxification is an important function of human peroxisomes. Glyoxylate is a highly reactive molecule, generated in the intermediary metabolism of glycine, hydroxyproline and glycolate mainly. Glyoxylate accumulation in the cytosol is readily transformed by lactate dehydrogenase into oxalate, a
Mohamed S Rashed et al.
Biomedical chromatography : BMC, 16(3), 191-198 (2002-03-29)
Glyceric acid is a highly polar chiral carboxylic acid that is usually not detected during routine organic acid analysis. Increased excretion is observed in two phenotypically distinct and rare inherited metabolic diseases, D-glyceric aciduria, and L-glyceric aciduria (also known as
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