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51738

Sigma-Aldrich

L-Glyceric acid sodium salt

≥95.0% (TLC)

Sinônimo(s):

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

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About This Item

Fórmula empírica (Notação de Hill):
C3H6O4 · xNa+
Número CAS:
28305-26-2
Peso molecular:
106.08 (free acid basis)
Número MDL:
MFCD01318549
Código UNSPSC:
12352201
NACRES:
NA.25

Nível de qualidade

100

Ensaio

≥95.0% (TLC)

Formulário

powder or crystals

atividade óptica

[α]/D -18.5±3.0°, c = 1 in H2O

cor

white

cadeia de caracteres SMILES

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-/m0/s1

chave InChI

RBNPOMFGQQGHHO-REOHCLBHSA-N

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Ações bioquímicas/fisiológicas

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

Outras notas

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

Código de classe de armazenamento

11 - Combustible Solids

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

Not applicable

Ponto de fulgor (°C)

Not applicable

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Certificados de análise (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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