N-((5-(butylthio)-4-ethyl-4H-1,2,4-triazol-3-yl)methyl)-4-chlorobenzenesulfonamide CAS 338422-03-0

Purity 97%+In StockPharmaceutical Standards
CAS No.338422-03-0
Molecular FormulaC15H21ClN4O2S2
Molecular Weight388.94 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

N-((5-(butylthio)-4-ethyl-4H-1,2,4-triazol-3-yl)methyl)-4-chlorobenzenesulfonamide CAS 338422-03-0 chemical structure

Description

Recommended for analytical method development and validation; each product is supplied with a full Certificate of Analysis (COA) ensuring ISO 17034 metrological traceability.

CATO supplies N-((5-(butylthio)-4-ethyl-4H-1,2,4-triazol-3-yl)methyl)-4-chlorobenzenesulfonamide (CAS 338422-03-0), a certified reference material (molecular formula C15H21ClN4O2S2, MW 388.94 g/mol) for analytical method development and quality control.

N-((5-(butylthio)-4-ethyl-4H-1,2,4-triazol-3-yl)methyl)-4-chlorobenzenesulfonamide (C15H21ClN4O2S2) contains a nitrogen-containing heterocyclic scaffold, an amide group, a sulfone group, a hydroxyl group, an ether linkage, chlorine substitution. It is notably hygroscopic, halogen substitution raises its density and boiling point, 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).

As a certified reference material (CRM), N-((5-(butylthio)-4-ethyl-4H-1,2,4-triazol-3-yl)methyl)-4-chlorobenzenesulfonamide 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 FormulaC15H21ClN4O2S2
Molecular Weight388.94 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)7.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)2025
Halogen ContentCl-containing
Nitrogen Atoms4
Sulfur Atoms2

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