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L-Glyceric acid sodium, a urinary metabolite, is predominantly found in individuals with the rare inherited metabolic disorder L-glyceric aciduria. This compound is a diagnostic tool for identifying primary hyperoxaluria type 2 (PH2) and distinguishing it from primary hyperoxaluria type 1 (PH1) based on its excretion pattern.
Description | L-Glyceric acid sodium, a urinary metabolite, is predominantly found in individuals with the rare inherited metabolic disorder L-glyceric aciduria. This compound is a diagnostic tool for identifying primary hyperoxaluria type 2 (PH2) and distinguishing it from primary hyperoxaluria type 1 (PH1) based on its excretion pattern. |
In vitro | Primary hyperoxaluria type 2 (PH2), or L-glyceric aciduria, results from deficiencies in D-glycerate dehydrogenase and glyoxylate reductase, leading to the excretion of L-glyceric acid, a key diagnostic marker for PH2[1][2]. |
Molecular Weight | 128.06 |
Formula | C3H5NaO4 |
Cas No. | 146298-95-5 |
Relative Density. | no data available |
Storage | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice. |
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