4-Chloro-N-(4-hydroxynaphthalen-1-yl)-3-nitrobenzenesulfonamide CAS 420092-79-1

Purity 97%+In StockPharmaceutical Standards
CAS No.420092-79-1
Molecular FormulaC16H11ClN2O5S
Molecular Weight378.79 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

4-Chloro-N-(4-hydroxynaphthalen-1-yl)-3-nitrobenzenesulfonamide CAS 420092-79-1 chemical structure

Description

The molecular framework of 4-Chloro-N-(4-hydroxynaphthalen-1-yl)-3-nitrobenzenesulfonamide (C16H11ClN2O5S) is characterized by a flavonoid core, an amide group, a sulfone group, a hydroxyl group, an ether linkage, chlorine 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).

CATO supplies 4-Chloro-N-(4-hydroxynaphthalen-1-yl)-3-nitrobenzenesulfonamide (CAS 420092-79-1), a certified reference material (molecular formula C16H11ClN2O5S, MW 378.79 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-N-(4-hydroxynaphthalen-1-yl)-3-nitrobenzenesulfonamide 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 FormulaC16H11ClN2O5S
Molecular Weight378.79 g/mol
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)12.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)2025
Halogen ContentCl-containing
Nitrogen Atoms2
Sulfur Atoms1

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