2-(Aminomethyl)-3-(difluoromethyl)-4-(trifluoromethyl)pyridine-5-sulfonamide CAS 1361702-20-6

Purity 97%+In StockPharmaceutical Standards
CAS No.1361702-20-6
Molecular FormulaC8H8F5N3O2S
Molecular Weight305.23 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

2-(Aminomethyl)-3-(difluoromethyl)-4-(trifluoromethyl)pyridine-5-sulfonamide CAS 1361702-20-6 chemical structure

Description

As a certified reference material (CRM), 2-(Aminomethyl)-3-(difluoromethyl)-4-(trifluoromethyl)pyridine-5-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.

2-(Aminomethyl)-3-(difluoromethyl)-4-(trifluoromethyl)pyridine-5-sulfonamide (CAS 1361702-20-6) is a high-purity analytical reference standard with the molecular formula C8H8F5N3O2S and a molecular weight of 305.23 g/mol.

Structurally, 2-(Aminomethyl)-3-(difluoromethyl)-4-(trifluoromethyl)pyridine-5-sulfonamide (C8H8F5N3O2S) contains a nitrogen-containing heterocyclic scaffold, an amide group, a sulfone group, a hydroxyl group, an ether linkage, fluorine substitution. The molecule exhibits a degree of unsaturation (DBE) of 4.0, corresponding to approximately 4 ring(s) or double-bond equivalent(s). With a molecular weight of 305.23 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.

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.

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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