3-Bromo-n-(piperidin-4-yl)benzenesulfonamide hydrochloride CAS 1233958-23-0

Purity 97%+In StockPharmaceutical Standards
CAS No.1233958-23-0
Molecular FormulaC11H15BrN2O2S
Molecular WeightN/A
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

3-Bromo-n-(piperidin-4-yl)benzenesulfonamide hydrochloride CAS 1233958-23-0 chemical structure

Description

3-Bromo-n-(piperidin-4-yl)benzenesulfonamide hydrochloride (C11H15BrN2O2SHCl) contains a nitrogen-containing heterocyclic scaffold, an amide group, a sulfone group, a hydroxyl group, an ether linkage, chlorine/bromine substitution. It is notably hygroscopic, halogen substitution raises its density and boiling point, its high carbon-to-hydrogen ratio confers good lipid solubility, the carboxyl group imparts weak acidity; these physicochemical properties determine the optimal preparation and storage of its standard solutions. The aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

CATO supplies 3-Bromo-n-(piperidin-4-yl)benzenesulfonamide hydrochloride (CAS 1233958-23-0), a certified reference material (molecular formula C11H15BrN2O2SHCl, MW 355.67 g/mol) for analytical method development and quality control.

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), 3-Bromo-n-(piperidin-4-yl)benzenesulfonamide hydrochloride 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 FormulaC11H15BrN2O2S HCl
Molecular Weight355.67 g/mol
Purity97%+
StorageStore at 2-8°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)4.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1990
Halogen ContentCl/Br-containing
Nitrogen Atoms2
Sulfur Atoms1

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