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51738

Sigma-Aldrich

L-Glycerinsäure Natriumsalz

≥95.0% (TLC)

Synonym(e):

(S)-2,3-Dihydroxypropansäure Natriumsalz, Natrium-L-glycerat

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About This Item

Empirische Formel (Hill-System):
C3H6O4 · xNa+
CAS-Nummer:
28305-26-2
Molekulargewicht:
106.08 (free acid basis)
UNSPSC-Code:
12352201
NACRES:
NA.25

Assay

≥95.0% (TLC)

Form

powder or crystals

Optische Aktivität

[α]/D -18.5±3.0°, c = 1 in H2O

Farbe

white

InChI

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

InChIKey

RBNPOMFGQQGHHO-REOHCLBHSA-N

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Biochem./physiol. Wirkung

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

Sonstige Hinweise

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

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Analysenzertifikate (COA)

Suchen Sie nach Analysenzertifikate (COA), indem Sie die Lot-/Chargennummer des Produkts eingeben. Lot- und Chargennummern sind auf dem Produktetikett hinter den Wörtern ‘Lot’ oder ‘Batch’ (Lot oder Charge) zu finden.

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Natriumoxalat reference material for titrimetry, certified by BAM, >99.5%

Supelco

71804

Natriumoxalat

D-(−)-3-Phosphoglycerinsäure Dinatriumsalz ≥93% dry basis (enzymatic), powder

Sigma-Aldrich

P8877

D-(−)-3-Phosphoglycerinsäure Dinatriumsalz

Glycolsäure ReagentPlus®, 99%

Sigma-Aldrich

124737

Glycolsäure

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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