51738
L-Glyceric acid sodium salt
≥95.0% (TLC)
Synonym(s):
(S)-2,3-Dihydroxypropanoic acid sodium salt, Sodium L-glycerate
Sign Into View Organizational & Contract Pricing
Select a Size
10 MG
€61.60
50 MG
€255.00
250 MG
€1,040.00
All Photos(1)
Select a Size
Change View
10 MG
€61.60
50 MG
€255.00
250 MG
€1,040.00
About This Item
Empirical Formula (Hill Notation):
C3H6O4 · xNa+
CAS Number:
Molecular Weight:
106.08 (free acid basis)
MDL number:
UNSPSC Code:
12352201
NACRES:
NA.25
Recommended Products
Assay
≥95.0% (TLC)
form
powder or crystals
optical activity
[α]/D -18.5±3.0°, c = 1 in H2O
color
white
SMILES string
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
InChI key
RBNPOMFGQQGHHO-REOHCLBHSA-N
Looking for similar products? Visit Product Comparison Guide
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
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Customers Also Viewed
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)
Active Filters
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service
