N-(4-Methoxybenzyl)-1-(2-nitrophenyl)methanamine CAS 7539-30-2

Purity 97%+In StockPharmaceutical Standards
CAS No.7539-30-2
Molecular FormulaC15H16N2O3
Molecular WeightN/A
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

N-(4-Methoxybenzyl)-1-(2-nitrophenyl)methanamine CAS 7539-30-2 chemical structure

Description

N-(4-Methoxybenzyl)-1-(2-nitrophenyl)methanamine (C15H16N2O3HBr) contains a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage, bromine substitution. It is notably hygroscopic, halogen substitution raises its density and boiling point, the carboxyl group imparts weak acidity; these physicochemical properties determine the optimal preparation and storage of its standard solutions. The aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

CATO supplies N-(4-Methoxybenzyl)-1-(2-nitrophenyl)methanamine (CAS 7539-30-2), a certified reference material (molecular formula C15H16N2O3HBr, MW 353.22 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.

CATO manufactures N-(4-Methoxybenzyl)-1-(2-nitrophenyl)methanamine 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 FormulaC15H16N2O3 HBr
Molecular Weight353.22 g/mol
AppearancePale yellow to yellow crystalline powder. (slight halide-like odor)
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; Contains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)8.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1959
Halogen ContentBr-containing
Nitrogen Atoms2

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