N-(4,6-Dimethylpyrimidin-2-yl)-4-(2-(2-phenyl-1H-indol-3-yl)hydrazinyl)benzenesulfonamide CAS 88152-01-6

Purity 97%+In StockPharmaceutical Standards
CAS No.88152-01-6
Molecular FormulaC26H24N6O2S
Molecular Weight484.57 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

N-(4,6-Dimethylpyrimidin-2-yl)-4-(2-(2-phenyl-1H-indol-3-yl)hydrazinyl)benzenesulfonamide CAS 88152-01-6 chemical structure

Description

CATO supplies N-(4,6-Dimethylpyrimidin-2-yl)-4-(2-(2-phenyl-1H-indol-3-yl)hydrazinyl)benzenesulfonamide (CAS 88152-01-6), a certified reference material (molecular formula C26H24N6O2S, MW 484.57 g/mol) for analytical method development and quality control.

N-(4,6-Dimethylpyrimidin-2-yl)-4-(2-(2-phenyl-1H-indol-3-yl)hydrazinyl)benzenesulfonamide (C26H24N6O2S) contains a steroid core, an amide group, a sulfone group, a hydroxyl group, an ether linkage. It is notably hygroscopic, the carboxyl group imparts weak acidity; these physicochemical properties determine the optimal preparation and storage of its standard solutions. Nitrogen-containing functional groups confer excellent ionization efficiency in positive-ion electrospray (ESI) mode, making the compound well suited to LC-MS/MS analysis.

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 FormulaC26H24N6O2S
Molecular Weight484.57 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
Degree of Unsaturation (DBE)18.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1982
Nitrogen Atoms6
Sulfur Atoms1

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