3,4-Dimethylimidazo[4,5-f]Quinoxalin-2-Amine CAS 108354-48-9

Purity 97%+In StockPharmaceutical Standards
CAS No.108354-48-9
Molecular FormulaC11H11N5
Molecular Weight213.24 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

3,4-Dimethylimidazo[4,5-f]Quinoxalin-2-Amine CAS 108354-48-9 chemical structure

Description

Under current pharmacopoeial and regulatory frameworks, quality-control requirements for this class of reference material explicitly involve the control of targets including 3,4-Dimethylimidazo[4,5-f]Quinoxalin-2-Amine.

CATO supplies 3,4-Dimethylimidazo[4,5-f]Quinoxalin-2-Amine (CAS 108354-48-9), a certified reference material (molecular formula C11H11N5, MW 213.24 g/mol) for analytical method development and quality control.

The molecular framework of 3,4-Dimethylimidazo[4,5-f]Quinoxalin-2-Amine (C11H11N5) is characterized by a nitrogen-containing heterocyclic scaffold, a nitrile group. In reversed-phase chromatography, its retention is governed primarily by the protonation state of its nitrogen-containing groups, which provides a practical basis for HPLC-UV/DAD or LC-MS method development. 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 FormulaC11H11N5
Molecular Weight213.24 g/mol
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)9.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1987
Nitrogen Atoms5

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