N-(3-Hydroxy-4-iodophenyl)methanesulfonamide CAS 1243391-32-3

Purity 97%+In StockPharmaceutical Standards
CAS No.1243391-32-3
Molecular FormulaC7H8INO3S
Molecular Weight313.11 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

N-(3-Hydroxy-4-iodophenyl)methanesulfonamide CAS 1243391-32-3 chemical structure

Description

N-(3-Hydroxy-4-iodophenyl)methanesulfonamide (CAS 1243391-32-3), molecular formula C7H8INO3S and molecular weight 313.11 g/mol, is a CATO reference standard with documented purity and traceability.

N-(3-Hydroxy-4-iodophenyl)methanesulfonamide (C7H8INO3S) contains an amide group, a sulfone group, a carboxylic acid group, a hydroxyl group, an ether linkage, iodine substitution, an aromatic ring system. It is notably hygroscopic, halogen substitution raises its density and boiling point, the carboxyl group imparts weak acidity; these physicochemical properties determine the optimal preparation and storage of its standard solutions. 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.

As a certified reference material (CRM), N-(3-Hydroxy-4-iodophenyl)methanesulfonamide 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 FormulaC7H8INO3S
Molecular Weight313.11 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.)1990
Halogen ContentI-containing
Nitrogen Atoms1
Sulfur Atoms1

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