2-[4-(4-aminophenoxy)phenyl]acetonitrile hydrochloride CAS 1211298-86-0

Purity 97%+In StockPharmaceutical Standards
CAS No.1211298-86-0
Molecular FormulaC14H12N2O
Molecular WeightN/A
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

2-[4-(4-aminophenoxy)phenyl]acetonitrile hydrochloride CAS 1211298-86-0 chemical structure

Description

As a certified reference material (CRM), 2-[4-(4-aminophenoxy)phenyl]acetonitrile 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.

CATO supplies 2-[4-(4-aminophenoxy)phenyl]acetonitrile hydrochloride (CAS 1211298-86-0), a certified reference material (molecular formula C14H12N2OHCl, MW 260.72 g/mol) for analytical method development and quality control.

The molecular framework of 2-[4-(4-aminophenoxy)phenyl]acetonitrile hydrochloride (C14H12N2OHCl) is characterized by a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage, 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.

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.

Physical & Chemical Properties

Molecular FormulaC14H12N2O HCl
Molecular Weight260.72 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)9.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1990
Halogen ContentCl-containing
Nitrogen Atoms2

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