6-Butyl-2-chloroimidazo[1,2-b]pyridazine-3-sulfonamide CAS 570416-08-9

Purity 97%+In StockPharmaceutical Standards
CAS No.570416-08-9
Molecular FormulaC10H13ClN4O2S
Molecular Weight288.75 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

6-Butyl-2-chloroimidazo[1,2-b]pyridazine-3-sulfonamide CAS 570416-08-9 chemical structure

Description

The molecular framework of 6-Butyl-2-chloroimidazo[1,2-b]pyridazine-3-sulfonamide (C10H13ClN4O2S) is characterized by a nitrogen-containing heterocyclic scaffold, an amide group, a sulfone group, a hydroxyl group, an ether linkage, chlorine 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 presence of an aromatic ring or conjugated system gives the compound characteristic absorption bands in the UV-Vis region, making it well suited to UV or diode-array detection (DAD).

6-Butyl-2-chloroimidazo[1,2-b]pyridazine-3-sulfonamide (CAS 570416-08-9) is a high-purity analytical reference standard with the molecular formula C10H13ClN4O2S and a molecular weight of 288.75 g/mol.

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), 6-Butyl-2-chloroimidazo[1,2-b]pyridazine-3-sulfonamide 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 FormulaC10H13ClN4O2S
Molecular Weight288.75 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light, keep sealed and dry, keep tightly closed to prevent evaporation
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)6.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1984
Halogen ContentCl-containing
Nitrogen Atoms4
Sulfur Atoms1

Related Butyl Standards

Recommended Standards

Why CATO?