O1-tert-Butyl O2-methyl (2S,4R)-4-aminopyrrolidine-1,2-dicarboxylate oxalic acid CAS 1807938-33-5

Purity 97%+In StockPharmaceutical Standards
CAS No.1807938-33-5
Molecular FormulaC11H20N2O4
Molecular WeightN/A
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

O1-tert-Butyl O2-methyl (2S,4R)-4-aminopyrrolidine-1,2-dicarboxylate oxalic acid CAS 1807938-33-5 chemical structure

Description

CATO supplies O1-tert-Butyl O2-methyl (2S,4R)-4-aminopyrrolidine-1,2-dicarboxylate oxalic acid (CAS 1807938-33-5), a certified reference material (molecular formula C11H20N2O4C2H2O4, MW 334.32 g/mol) for analytical method development and quality control.

O1-tert-Butyl O2-methyl (2S,4R)-4-aminopyrrolidine-1,2-dicarboxylate oxalic acid (C11H20N2O4C2H2O4) contains a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage. It is notably hygroscopic, the carboxyl group imparts weak acidity; these physicochemical properties determine the optimal preparation and storage of its standard solutions. Nitrogen-containing functional groups confer excellent ionization efficiency in positive-ion electrospray (ESI) mode, making the compound well suited to LC-MS/MS analysis.

This reference standard is suitable for quantitative analysis on major chromatographic platforms including HPLC, GC, LC-MS/MS, and GC-MS, serving as an external calibration standard or a system suitability test reference material.

The assigned purity is verified by mass-balance and quantitative NMR (qNMR) approaches, with the expanded uncertainty reported at a 95% confidence level (k=2). Batch homogeneity and stability are independently assessed for every lot.

Physical & Chemical Properties

Molecular FormulaC11H20N2O4 C2H2O4
Molecular Weight334.32 g/mol
AppearanceOff-white to pale yellow crystalline powder
Purity97%+
StorageStore at 2-8°C, protect from light, keep sealed and dry
Solubility (reference)Soluble in DMSO, DMF, methanol
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light; Hygroscopic; reseal immediately after opening
Degree of Unsaturation (DBE)4.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1995
Nitrogen Atoms2

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