N-(2-Fluorophenyl)benzenesulfonamide CAS 54129-13-4

Purity 97%+In StockPharmaceutical Standards
CAS No.54129-13-4
Molecular FormulaC12H10FNO2S
Molecular Weight251.28 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

N-(2-Fluorophenyl)benzenesulfonamide CAS 54129-13-4 chemical structure

Description

Compared with other compounds in its class, the molecular weight of 251.28 g/mol gives N-(2-Fluorophenyl)benzenesulfonamide distinctive chromatographic separation conditions and mass-spectrometry parameter settings.

N-(2-Fluorophenyl)benzenesulfonamide (CAS 54129-13-4) is a high-purity analytical reference standard with the molecular formula C12H10FNO2S and a molecular weight of 251.28 g/mol.

Owing to a nitrogen-containing heterocyclic scaffold, an amide group, a sulfone group, a hydroxyl group, an ether linkage, fluorine substitution, N-(2-Fluorophenyl)benzenesulfonamide is typically pale yellow to yellow crystalline powder. Its solid-state physicochemical attributes — including a molecular weight of 251.28 g/mol — guide the selection of appropriate sample preparation and analytical techniques. 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-(2-Fluorophenyl)benzenesulfonamide 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 FormulaC12H10FNO2S
Molecular Weight251.28 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light, keep tightly closed to prevent evaporation
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light; Contains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)8.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1972
Halogen ContentF-containing
Nitrogen Atoms1
Sulfur Atoms1

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