N,N-Dimethyl-2,3,4,5,6-Pentafluoroaniline CAS 1801-14-5

Purity 97%+In StockPharmaceutical Standards
CAS No.1801-14-5
Molecular FormulaC8H6F5N
Molecular Weight211.13 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

N,N-Dimethyl-2,3,4,5,6-Pentafluoroaniline CAS 1801-14-5 chemical structure

Description

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.

N,N-Dimethyl-2,3,4,5,6-Pentafluoroaniline (CAS 1801-14-5) is a high-purity analytical reference standard with the molecular formula C8H6F5N and a molecular weight of 211.13 g/mol.

Based on its molecular formula C8H6F5N, N,N-Dimethyl-2,3,4,5,6-Pentafluoroaniline contains a nitrogen-containing heterocyclic scaffold, a nitrile group, fluorine substitution; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 211.13 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. Nitrogen-containing functional groups confer excellent ionization efficiency in positive-ion electrospray (ESI) mode, making the compound well suited to LC-MS/MS analysis.

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 FormulaC8H6F5N
Molecular Weight211.13 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 methanol, acetonitrile, DMSO
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.)1957
Halogen ContentF-containing
Nitrogen Atoms1

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