3,5-Bis(4-fluorobenzenesulfonamido)benzoic acid CAS 329908-32-9

Purity 97%+In StockPharmaceutical Standards
CAS No.329908-32-9
Molecular FormulaC19H14F2N2O6S2
Molecular Weight468.45 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

3,5-Bis(4-fluorobenzenesulfonamido)benzoic acid CAS 329908-32-9 chemical structure

Description

Compared with other compounds in its class, the molecular weight of 468.45 g/mol gives 3,5-Bis(4-fluorobenzenesulfonamido)benzoic acid distinctive chromatographic separation conditions and mass-spectrometry parameter settings.

3,5-Bis(4-fluorobenzenesulfonamido)benzoic acid (CAS 329908-32-9), molecular formula C19H14F2N2O6S2 and molecular weight 468.45 g/mol, is a CATO reference standard with documented purity and traceability.

The molecular framework of 3,5-Bis(4-fluorobenzenesulfonamido)benzoic acid (C19H14F2N2O6S2) is characterized by a flavonoid core, an amide group, a sulfone group, a hydroxyl group, an ether linkage, fluorine 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. The aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

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 FormulaC19H14F2N2O6S2
Molecular Weight468.45 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)13.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)2025
Halogen ContentF-containing
Nitrogen Atoms2
Sulfur Atoms2

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