N-Phenyl-4-(quinolin-3-ylmethyl)piperazine-1-carboxamide CAS 898235-65-9

Purity 97%+In StockPharmaceutical Standards
CAS No.898235-65-9
Molecular FormulaC21H22N4O
Molecular Weight346.43 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

N-Phenyl-4-(quinolin-3-ylmethyl)piperazine-1-carboxamide CAS 898235-65-9 chemical structure

Description

Compared with other compounds in its class, the molecular weight of 346.43 g/mol gives N-Phenyl-4-(quinolin-3-ylmethyl)piperazine-1-carboxamide distinctive chromatographic separation conditions and mass-spectrometry parameter settings.

N-Phenyl-4-(quinolin-3-ylmethyl)piperazine-1-carboxamide (CAS 898235-65-9) is a high-purity analytical reference standard with the molecular formula C21H22N4O and a molecular weight of 346.43 g/mol.

N-Phenyl-4-(quinolin-3-ylmethyl)piperazine-1-carboxamide (C21H22N4O) contains a steroid core, an amide group, a hydroxyl group, an ether linkage. Its physicochemical properties are representative of its class; 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 FormulaC21H22N4O
Molecular Weight346.43 g/mol
AppearancePale yellow to yellow crystalline powder
Purity97%+
StorageStore at 2-8°C, protect from light
Solubility (reference)Soluble in DMSO, DMF, methanol
StabilityLight-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)13.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1987
Nitrogen Atoms4

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