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51738

Sigma-Aldrich

L-Glyceric acid sodium salt

≥95.0% (TLC)

Synonym(s):

(S)-2,3-Dihydroxypropanoic acid sodium salt, Sodium L-glycerate

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About This Item

Empirical Formula (Hill Notation):
C3H6O4 · xNa+
CAS Number:
28305-26-2
Molecular Weight:
106.08 (free acid basis)
UNSPSC Code:
12352201
NACRES:
NA.25

Quality Level

100

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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Biochem/physiol Actions

L-Glyceric aciduria is a well known indicator for primary hyperoxaluria type II (MIM ID 260000).

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

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Pierre Cochat et al.
Pediatric nephrology (Berlin, Germany), 25(3), 415-424 (2009-01-22)
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
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
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
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
Identification and location of L-glycerate, an unusual acyl substituent in gellan gum.
Kuo, M.S. and Mort, A.J.
Carbohydrate Research, 156, 173-187 (1986)

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