4-Chloro-2-(4,5-dihydro-1H-imidazol-2-yl)isoindoline hydrochloride CAS 204274-74-8

Purity 97%+In StockPharmaceutical Standards
CAS No.204274-74-8
Molecular FormulaC11H12ClN3
Molecular WeightN/A
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

4-Chloro-2-(4,5-dihydro-1H-imidazol-2-yl)isoindoline hydrochloride CAS 204274-74-8 chemical structure

Description

The molecular framework of 4-Chloro-2-(4,5-dihydro-1H-imidazol-2-yl)isoindoline hydrochloride (C11H12ClN3HCl) is characterized by a nitrogen-containing heterocyclic scaffold, a nitrile group, chlorine substitution. In reversed-phase chromatography, its retention is governed primarily by its high hydrophobicity (logP), which provides a practical basis for HPLC-UV/DAD or LC-MS method development. Halogen substitution (F/Cl/Br/I) produces a distinctive isotope pattern in mass spectrometry, a valuable aid for qualitative confirmation.

CATO supplies 4-Chloro-2-(4,5-dihydro-1H-imidazol-2-yl)isoindoline hydrochloride (CAS 204274-74-8), a certified reference material (molecular formula C11H12ClN3HCl, MW 258.15 g/mol) for analytical method development and quality control.

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), 4-Chloro-2-(4,5-dihydro-1H-imidazol-2-yl)isoindoline 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 FormulaC11H12ClN3 HCl
Molecular Weight258.15 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)6.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)2015
Halogen ContentCl-containing
Nitrogen Atoms3

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