1-N-(4-methoxyphenyl)benzene-1,2-diamine CAS 25914-22-1

Purity 97%+In StockPharmaceutical Standards
CAS No.25914-22-1
Molecular FormulaC13H14N2O
Molecular WeightN/A
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

1-N-(4-methoxyphenyl)benzene-1,2-diamine CAS 25914-22-1 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 1-N-(4-methoxyphenyl)benzene-1,2-diamine.

1-N-(4-methoxyphenyl)benzene-1,2-diamine (CAS 25914-22-1) is a high-purity analytical reference standard with the molecular formula C13H14N2OHCl and a molecular weight of 250.73 g/mol.

The molecular framework of 1-N-(4-methoxyphenyl)benzene-1,2-diamine (C13H14N2OHCl) 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.

CATO manufactures 1-N-(4-methoxyphenyl)benzene-1,2-diamine under ISO 17034:2016 accreditation with dual CNAS and ANAB accreditation. Each batch is characterized by orthogonal methods and supplied with a full Certificate of Analysis (COA), ensuring metrological traceability.

Physical & Chemical Properties

Molecular FormulaC13H14N2O HCl
Molecular Weight250.73 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)7.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1964
Halogen ContentCl-containing
Nitrogen Atoms2

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