2-Chloro-6-methyl-4-(trifluoromethyl)nicotinonitrile CAS 13600-48-1

Purity 97%+In StockPharmaceutical Standards
CAS No.13600-48-1
Molecular FormulaC8H4ClF3N2
Molecular Weight220.58 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

2-Chloro-6-methyl-4-(trifluoromethyl)nicotinonitrile CAS 13600-48-1 chemical structure

Description

2-Chloro-6-methyl-4-(trifluoromethyl)nicotinonitrile (C8H4ClF3N2) contains a nitrogen-containing heterocyclic scaffold, a nitrile group, fluorine/chlorine substitution. Halogen substitution raises its density and boiling point; these physicochemical properties determine the optimal preparation and storage of its standard solutions. Nitrogen-containing functional groups confer excellent ionization efficiency in positive-ion electrospray (ESI) mode, making the compound well suited to LC-MS/MS analysis.

2-Chloro-6-methyl-4-(trifluoromethyl)nicotinonitrile (CAS 13600-48-1) is a high-purity analytical reference standard with the molecular formula C8H4ClF3N2 and a molecular weight of 220.58 g/mol.

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.

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 FormulaC8H4ClF3N2
Molecular Weight220.58 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)6.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1960
Halogen ContentF/Cl-containing
Nitrogen Atoms2

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