1-(5-Bromo-2-nitrophenyl)-1,4-diazepane CAS 1494015-51-8

Purity 97%+In StockPharmaceutical Standards
CAS No.1494015-51-8
Molecular FormulaC11H14BrN3O2
Molecular Weight300.15 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

1-(5-Bromo-2-nitrophenyl)-1,4-diazepane CAS 1494015-51-8 chemical structure

Description

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 supplies 1-(5-Bromo-2-nitrophenyl)-1,4-diazepane (CAS 1494015-51-8), a certified reference material (molecular formula C11H14BrN3O2, MW 300.15 g/mol) for analytical method development and quality control.

The molecular framework of 1-(5-Bromo-2-nitrophenyl)-1,4-diazepane (C11H14BrN3O2) is characterized by a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage, bromine substitution. 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. The aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

As a certified reference material (CRM), 1-(5-Bromo-2-nitrophenyl)-1,4-diazepane 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 FormulaC11H14BrN3O2
Molecular Weight300.15 g/mol
AppearanceOff-white to pale 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)6.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1992
Halogen ContentBr-containing
Nitrogen Atoms3

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