4-Cyclopropoxy-N-methyl-2-(trifluoromethyl)pyridin-3-amine CAS 1243375-27-0

Purity 97%+In StockPharmaceutical Standards
CAS No.1243375-27-0
Molecular FormulaC10H11F3N2O
Molecular Weight232.20 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

4-Cyclopropoxy-N-methyl-2-(trifluoromethyl)pyridin-3-amine CAS 1243375-27-0 chemical structure

Description

4-Cyclopropoxy-N-methyl-2-(trifluoromethyl)pyridin-3-amine (C10H11F3N2O) contains a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage, 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 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).

4-Cyclopropoxy-N-methyl-2-(trifluoromethyl)pyridin-3-amine (CAS 1243375-27-0), molecular formula C10H11F3N2O and molecular weight 232.20 g/mol, is a CATO reference standard with documented purity and traceability.

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

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 FormulaC10H11F3N2O
Molecular Weight232.20 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)5.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1990
Halogen ContentF-containing
Nitrogen Atoms2

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