4-(Aminomethyl)-6-(difluoromethyl)-5-(trifluoromethyl)pyridine-3-sulfonamide CAS 1361815-45-3

Purity 97%+In StockPharmaceutical Standards
CAS No.1361815-45-3
Molecular FormulaC8H8F5N3O2S
Molecular Weight305.23 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

4-(Aminomethyl)-6-(difluoromethyl)-5-(trifluoromethyl)pyridine-3-sulfonamide CAS 1361815-45-3 chemical structure

Description

CATO supplies 4-(Aminomethyl)-6-(difluoromethyl)-5-(trifluoromethyl)pyridine-3-sulfonamide (CAS 1361815-45-3), a certified reference material (molecular formula C8H8F5N3O2S, MW 305.23 g/mol) for analytical method development and quality control.

Based on its molecular formula C8H8F5N3O2S, 4-(Aminomethyl)-6-(difluoromethyl)-5-(trifluoromethyl)pyridine-3-sulfonamide contains a nitrogen-containing heterocyclic scaffold, an amide group, a sulfone group, a hydroxyl group, an ether linkage, fluorine substitution; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 305.23 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. Nitrogen-containing functional groups confer excellent ionization efficiency in positive-ion electrospray (ESI) mode, making the compound well suited to LC-MS/MS analysis.

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

As a certified reference material (CRM), 4-(Aminomethyl)-6-(difluoromethyl)-5-(trifluoromethyl)pyridine-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 FormulaC8H8F5N3O2S
Molecular Weight305.23 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.)1991
Halogen ContentF-containing
Nitrogen Atoms3
Sulfur Atoms1

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