(3-Fluoro-5-(trifluoromethyl)pyridin-2-yl)methanamine CAS 1260892-22-5

Purity 97%+In StockPharmaceutical Standards
CAS No.1260892-22-5
Molecular FormulaC7H6F4N2
Molecular Weight194.13 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

(3-Fluoro-5-(trifluoromethyl)pyridin-2-yl)methanamine CAS 1260892-22-5 chemical structure

Description

CATO manufactures (3-Fluoro-5-(trifluoromethyl)pyridin-2-yl)methanamine under ISO 17034:2016 accreditation with dual CNAS and ANAB accreditation. Each batch is characterized by orthogonal methods and supplied with a full Certificate of Analysis (COA), ensuring metrological traceability.

(3-Fluoro-5-(trifluoromethyl)pyridin-2-yl)methanamine (CAS 1260892-22-5) is a high-purity analytical reference standard with the molecular formula C7H6F4N2 and a molecular weight of 194.13 g/mol.

The molecular framework of (3-Fluoro-5-(trifluoromethyl)pyridin-2-yl)methanamine (C7H6F4N2) is characterized by a nitrile group, 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 presence of an aromatic ring or conjugated system gives the compound characteristic absorption bands in the UV-Vis region, making it well suited to UV or diode-array detection (DAD).

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 FormulaC7H6F4N2
Molecular Weight194.13 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)4.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1990
Halogen ContentF-containing
Nitrogen Atoms2

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