4-Nitro-N-(phenyl-l3-iodaneylidene)benzenesulfonamide CAS 149552-43-2

Purity 97%+In StockPharmaceutical Standards
CAS No.149552-43-2
Molecular FormulaC12H9IN2O4S
Molecular Weight404.18 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

4-Nitro-N-(phenyl-l3-iodaneylidene)benzenesulfonamide CAS 149552-43-2 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 4-Nitro-N-(phenyl-l3-iodaneylidene)benzenesulfonamide.

CATO supplies 4-Nitro-N-(phenyl-l3-iodaneylidene)benzenesulfonamide (CAS 149552-43-2), a certified reference material (molecular formula C12H9IN2O4S, MW 404.18 g/mol) for analytical method development and quality control.

The molecular framework of 4-Nitro-N-(phenyl-l3-iodaneylidene)benzenesulfonamide (C12H9IN2O4S) is characterized by a nitrogen-containing heterocyclic scaffold, an amide group, a sulfone group, a hydroxyl group, an ether linkage, iodine 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. 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.

The assigned purity is verified by mass-balance and quantitative NMR (qNMR) approaches, with the expanded uncertainty reported at a 95% confidence level (k=2). Batch homogeneity and stability are independently assessed for every lot.

Physical & Chemical Properties

Molecular FormulaC12H9IN2O4S
Molecular Weight404.18 g/mol
Purity97%+
StorageStore in a cool place (≤25°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)9.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1999
Halogen ContentI-containing
Nitrogen Atoms2
Sulfur Atoms1

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