N-Phenyl-2-(pyridin-4-yl)quinoline-4-carboxamide CAS 879921-41-2

Purity 97%+In StockPharmaceutical Standards
CAS No.879921-41-2
Molecular FormulaC21H15N3O
Molecular Weight325.36 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

N-Phenyl-2-(pyridin-4-yl)quinoline-4-carboxamide CAS 879921-41-2 chemical structure

Description

Compared with other compounds in its class, the molecular weight of 325.36 g/mol gives N-Phenyl-2-(pyridin-4-yl)quinoline-4-carboxamide distinctive chromatographic separation conditions and mass-spectrometry parameter settings.

N-Phenyl-2-(pyridin-4-yl)quinoline-4-carboxamide (CAS 879921-41-2) is a high-purity analytical reference standard with the molecular formula C21H15N3O and a molecular weight of 325.36 g/mol.

Based on its molecular formula C21H15N3O, N-Phenyl-2-(pyridin-4-yl)quinoline-4-carboxamide contains a steroid core, an amide group, a hydroxyl group, an ether linkage; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 325.36 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. The high carbon-to-hydrogen ratio imparts good lipophilicity, allowing liquid-liquid extraction with non-polar solvents such as n-hexane or ethyl acetate.

Recommended for analytical method development and validation; each product is supplied with a full Certificate of Analysis (COA) ensuring ISO 17034 metrological traceability.

As a certified reference material (CRM), N-Phenyl-2-(pyridin-4-yl)quinoline-4-carboxamide 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 FormulaC21H15N3O
Molecular Weight325.36 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)16.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1987
Nitrogen Atoms3

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