4-(Trifluoromethyl)-1,4,5,6-tetrahydropyridine-3-carbonitrile CAS 845866-48-0

Purity 97%+In StockPharmaceutical Standards
CAS No.845866-48-0
Molecular FormulaC7H7F3N2
Molecular Weight176.14 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

4-(Trifluoromethyl)-1,4,5,6-tetrahydropyridine-3-carbonitrile CAS 845866-48-0 chemical structure

Description

As a certified reference material (CRM), 4-(Trifluoromethyl)-1,4,5,6-tetrahydropyridine-3-carbonitrile 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.

CATO supplies 4-(Trifluoromethyl)-1,4,5,6-tetrahydropyridine-3-carbonitrile (CAS 845866-48-0), a certified reference material (molecular formula C7H7F3N2, MW 176.14 g/mol) for analytical method development and quality control.

4-(Trifluoromethyl)-1,4,5,6-tetrahydropyridine-3-carbonitrile (C7H7F3N2) contains a nitrile group, fluorine substitution, an aromatic ring system. Halogen substitution raises its density and boiling point; 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).

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 FormulaC7H7F3N2
Molecular Weight176.14 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.)1987
Halogen ContentF-containing
Nitrogen Atoms2

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