2-(trifluoromethyl)pyridine-5-thiocarboxamide 3-pyridinecarbothioamide, 6-(trifluoromethyl)- 386715-34-0 6-(Trifluoromethyl)thionicotinamide CAS 386715-34-0

Purity 97%+In StockPharmaceutical Standards
CAS No.386715-34-0
Molecular FormulaC7H5F3N2S
Molecular Weight206.19 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

2-(trifluoromethyl)pyridine-5-thiocarboxamide
3-pyridinecarbothioamide, 6-(trifluoromethyl)-
386715-34-0
6-(Trifluoromethyl)thionicotinamide CAS 386715-34-0 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 2-(trifluoromethyl)pyridine-5-thiocarboxamide 3-pyridinecarbothioamide, 6-(trifluoromethyl)- 386715-34-0 6-(Trifluoromethyl)thionicotinamide (CAS 386715-34-0), a certified reference material (molecular formula C7H5F3N2S, MW 206.19 g/mol) for analytical method development and quality control.

The molecular framework of 2-(trifluoromethyl)pyridine-5-thiocarboxamide 3-pyridinecarbothioamide, 6-(trifluoromethyl)- 386715-34-0 6-(Trifluoromethyl)thionicotinamide (C7H5F3N2S) is characterized by a nitrile group, sulfur-containing functionality, fluorine substitution, an aromatic ring system. 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 aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

The assigned purity is verified by mass-balance and quantitative NMR (qNMR) approaches, with the expanded uncertainty reported at a 95% confidence level (k=2). Batch homogeneity and stability are independently assessed for every lot.

Physical & Chemical Properties

Molecular FormulaC7H5F3N2S
Molecular Weight206.19 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light, 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
Degree of Unsaturation (DBE)5.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)2025
Halogen ContentF-containing
Nitrogen Atoms2
Sulfur Atoms1

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