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L-Glyceric acidL Glyceric acid is a mainly urinary metabolite accumulating in rare inherited metabolic disease L glyceric aciduria. L Glyceric acid can be used to diagnose primary hyperoxaluria type 2 (PH2). L Glyceric acid excretion to distinguish PH1 from PH2. Product information CAS Number: 28305 26 2 Molecular Weight: 106. 08 Formula: C3H6O4 Chemical Name: (2S) 2,3 dihydroxypropanoic acid Smiles: OC[C@H](O)C(O)=O InChiKey: RBNPOMFGQQGHHO REOHCLBHSA N InChi:
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L-Glyceric acid is a mainly urinary metabolite accumulating in rare inherited metabolic disease L-glyceric aciduria. L-Glyceric acid can be used to diagnose primary hyperoxaluria type 2 (PH2). L-Glyceric acid excretion to distinguish PH1 from PH2.

Product information

CAS Number: 28305-26-2

Molecular Weight: 106.08

Formula: C3H6O4

Chemical Name: (2S)-2,3-dihydroxypropanoic acid

Smiles: OC[C@H](O)C(O)=O

InChiKey: RBNPOMFGQQGHHO-REOHCLBHSA-N

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

Technical Data

Appearance: Solid Power

Purity: ≥98% (or refer to the Certificate of Analysis)

Shipping Condition: Shipped under ambient temperature as non-hazardous chemical or refer to Certificate of Analysis

Storage Condition: Dry, dark and -20 oC for 1 year or refer to the Certificate of Analysis.

Shelf Life: ≥12 months if stored properly.

Stock Solution Storage: 0 - 4 oC for 1 month or refer to the Certificate of Analysis.

Drug Formulation: To be determined

HS Tariff Code: 382200

How to use

In Vitro:

Primary hyperoxaluria type 2 (PH2), also called L-glyceric aciduria. The metabolic defect is due to deficiencies of D-glycerate dehydrogenase and glyoxylate reductase, leading to excretion of L-Glyceric acid, and L-Glyceric acid is the cornerstone for the diagnosis of PH2.

Products are for research use only. Not for human use.

L-Glyceric acid

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