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51738

Sigma-Aldrich

L-Glyceric acid sodium salt

≥95.0% (TLC)

Sinonimo/i:

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

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About This Item

Formula empirica (notazione di Hill):
C3H6O4 · xNa+
Numero CAS:
28305-26-2
Peso molecolare:
106.08 (free acid basis)
Codice UNSPSC:
12352201
NACRES:
NA.25

Livello qualitativo

100

Saggio

≥95.0% (TLC)

Stato

powder or crystals

Attività ottica

[α]/D -18.5±3.0°, c = 1 in H2O

Colore

white

InChI

1S/C3H6O4/c4-1-2(5)3(6)7/h2,4-5H,1H2,(H,6,7)/t2-/m0/s1
RBNPOMFGQQGHHO-REOHCLBHSA-N

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Azioni biochim/fisiol

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

Altre note

To gain a comprehensive understanding of our extensive range of Monosaccharides for your research, we encourage you to visit our Carbohydrates Category page.

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

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Certificati d'analisi (COA)

Lot/Batch Number
BCCF2337
BCCC6702
BCBM7156V
BCBM7156

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Sodium oxalate reference material for titrimetry, certified by BAM, >99.5%

Supelco

71804

Sodium oxalate

D-(−)-3-Phosphoglyceric acid disodium salt ≥93% dry basis (enzymatic), powder

Sigma-Aldrich

P8877

D-(−)-3-Phosphoglyceric acid disodium salt

Glycolic acid ReagentPlus®, 99%

Sigma-Aldrich

124737

Glycolic acid

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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