3-(1-Methyl-4-(trifluoromethyl)-1H-imidazol-2-yl)pyridine CAS 63875-04-7

Purity 97%+In StockPharmaceutical Standards
CAS No.63875-04-7
Molecular FormulaC10H8F3N3
Molecular Weight227.19 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

3-(1-Methyl-4-(trifluoromethyl)-1H-imidazol-2-yl)pyridine CAS 63875-04-7 chemical structure

Description

3-(1-Methyl-4-(trifluoromethyl)-1H-imidazol-2-yl)pyridine (C10H8F3N3) contains a nitrogen-containing heterocyclic scaffold, a nitrile group, fluorine substitution. Halogen substitution raises its density and boiling point, its high carbon-to-hydrogen ratio confers good lipid solubility; 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).

CATO supplies 3-(1-Methyl-4-(trifluoromethyl)-1H-imidazol-2-yl)pyridine (CAS 63875-04-7), a certified reference material (molecular formula C10H8F3N3, MW 227.19 g/mol) for analytical method development and quality control.

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), 3-(1-Methyl-4-(trifluoromethyl)-1H-imidazol-2-yl)pyridine 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 FormulaC10H8F3N3
Molecular Weight227.19 g/mol
AppearanceOff-white to pale yellow crystalline powder. (slight halide-like odor, faint amine-like odor, low volatility)
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)7.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1975
Halogen ContentF-containing
Nitrogen Atoms3

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