3-amino-N-phenylpyrrolidine-1-carboxamide hydrochloride CAS 1803583-99-4

Purity 97%+In StockPharmaceutical Standards
CAS No.1803583-99-4
Molecular FormulaC11H15N3O
Molecular WeightN/A
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

3-amino-N-phenylpyrrolidine-1-carboxamide hydrochloride CAS 1803583-99-4 chemical structure

Description

3-amino-N-phenylpyrrolidine-1-carboxamide hydrochloride (CAS 1803583-99-4) is a high-purity analytical reference standard with the molecular formula C11H15N3OHCl and a molecular weight of 241.72 g/mol.

Structurally, 3-amino-N-phenylpyrrolidine-1-carboxamide hydrochloride (C11H15N3OHCl) contains a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage, chlorine substitution. The molecule exhibits a degree of unsaturation (DBE) of 5.0, corresponding to approximately 5 ring(s) or double-bond equivalent(s). With a molecular weight of 241.72 g/mol, it falls into the medium-molecular-weight range. 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.

As a certified reference material (CRM), 3-amino-N-phenylpyrrolidine-1-carboxamide hydrochloride meets the metrological traceability requirements of ISO/IEC 17025 laboratories. Batch-to-batch consistency is monitored via control charts to guarantee comparable assigned values across lots.

Physical & Chemical Properties

Molecular FormulaC11H15N3O HCl
Molecular Weight241.72 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light, keep tightly closed to prevent evaporation
Solubility (reference)Soluble in DMSO, DMF, methanol
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)5.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1995
Halogen ContentCl-containing
Nitrogen Atoms3

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