Benzenesulfonamide, 4-bromo-N-(4-bromo-2-nitrophenyl)- CAS 10589-69-2

Purity 97%+In StockPharmaceutical Standards
CAS No.10589-69-2
Molecular FormulaC12H8Br2N2O4S
Molecular Weight436.08 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

Benzenesulfonamide, 4-bromo-N-(4-bromo-2-nitrophenyl)- CAS 10589-69-2 chemical structure

Description

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.

Benzenesulfonamide, 4-bromo-N-(4-bromo-2-nitrophenyl)- (CAS 10589-69-2), molecular formula C12H8Br2N2O4S and molecular weight 436.08 g/mol, is a CATO reference standard with documented purity and traceability.

Structurally, Benzenesulfonamide, 4-bromo-N-(4-bromo-2-nitrophenyl)- (C12H8Br2N2O4S) contains a nitrogen-containing heterocyclic scaffold, an amide group, a sulfone group, a hydroxyl group, an ether linkage, bromine substitution. The molecule exhibits a degree of unsaturation (DBE) of 9.0, corresponding to approximately 9 ring(s) or double-bond equivalent(s). With a molecular weight of 436.08 g/mol, it falls into the moderately-high-molecular-weight range. Halogen substitution (F/Cl/Br/I) produces a distinctive isotope pattern in mass spectrometry, a valuable aid for qualitative confirmation.

As a certified reference material (CRM), Benzenesulfonamide, 4-bromo-N-(4-bromo-2-nitrophenyl)- 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 FormulaC12H8Br2N2O4S
Molecular Weight436.08 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)9.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1960
Halogen ContentBr-containing
Nitrogen Atoms2
Sulfur Atoms1

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