4-(4-aminophenoxy)-7-methoxyquinoline-6-carboxamide CAS 417722-79-3

Purity 97%+In StockPharmaceutical Standards
CAS No.417722-79-3
Molecular FormulaC17H15N3O3
Molecular Weight309.32 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

4-(4-aminophenoxy)-7-methoxyquinoline-6-carboxamide CAS 417722-79-3 chemical structure

Description

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.

CATO supplies 4-(4-aminophenoxy)-7-methoxyquinoline-6-carboxamide (CAS 417722-79-3), a certified reference material (molecular formula C17H15N3O3, MW 309.32 g/mol) for analytical method development and quality control.

Structurally, 4-(4-aminophenoxy)-7-methoxyquinoline-6-carboxamide (C17H15N3O3) contains a steroid core, an amide group, a hydroxyl group, an ether linkage. The molecule exhibits a degree of unsaturation (DBE) of 12.0, corresponding to approximately 12 ring(s) or double-bond equivalent(s). With a molecular weight of 309.32 g/mol, it falls into the moderately-high-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.

As a certified reference material (CRM), 4-(4-aminophenoxy)-7-methoxyquinoline-6-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 FormulaC17H15N3O3
Molecular Weight309.32 g/mol
AppearancePale yellow to 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)12.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)2025
Nitrogen Atoms3

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