2-(Difluoromethyl)-5-hydroxy-3-iodopyridine-6-sulfonamide CAS 1807071-72-2

Purity 97%+In StockPharmaceutical Standards
CAS No.1807071-72-2
Molecular FormulaC6H5F2IN2O3S
Molecular Weight350.08 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

2-(Difluoromethyl)-5-hydroxy-3-iodopyridine-6-sulfonamide CAS 1807071-72-2 chemical structure

Description

The molecular framework of 2-(Difluoromethyl)-5-hydroxy-3-iodopyridine-6-sulfonamide (C6H5F2IN2O3S) is characterized by an amide group, a sulfone group, a carboxylic acid group, a hydroxyl group, an ether linkage, fluorine/iodine substitution, an aromatic ring system. 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).

2-(Difluoromethyl)-5-hydroxy-3-iodopyridine-6-sulfonamide (CAS 1807071-72-2) is a high-purity analytical reference standard with the molecular formula C6H5F2IN2O3S and a molecular weight of 350.08 g/mol.

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 2-(Difluoromethyl)-5-hydroxy-3-iodopyridine-6-sulfonamide 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 FormulaC6H5F2IN2O3S
Molecular Weight350.08 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light, keep sealed and dry
Solubility (reference)Soluble in methanol, ethanol, DMSO, water
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)4.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1995
Halogen ContentF/I-containing
Nitrogen Atoms2
Sulfur Atoms1

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