(2-Chlorophenyl)(4-(4-chlorophenyl)piperazin-1-yl)methanone CAS 420093-67-0

Purity 97%+In StockPharmaceutical Standards
CAS No.420093-67-0
Molecular FormulaC17H16Cl2N2O
Molecular Weight335.23 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

(2-Chlorophenyl)(4-(4-chlorophenyl)piperazin-1-yl)methanone CAS 420093-67-0 chemical structure

Description

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.

CATO supplies (2-Chlorophenyl)(4-(4-chlorophenyl)piperazin-1-yl)methanone (CAS 420093-67-0), a certified reference material (molecular formula C17H16Cl2N2O, MW 335.23 g/mol) for analytical method development and quality control.

Based on its molecular formula C17H16Cl2N2O, (2-Chlorophenyl)(4-(4-chlorophenyl)piperazin-1-yl)methanone contains a steroid core, an amide group, a hydroxyl group, an ether linkage, chlorine substitution; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 335.23 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.

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 FormulaC17H16Cl2N2O
Molecular Weight335.23 g/mol
AppearancePale yellow to yellow crystalline powder. (slight halide-like odor, low volatility)
Purity97%+
StorageStore at 2-8°C, protect from light
Solubility (reference)Soluble in DMSO, DMF, methanol
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)10.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)2025
Halogen ContentCl-containing
Nitrogen Atoms2

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