6-Chloro-9-(4-chlorophenoxy)-2-methoxyacridine CAS 115960-63-9

Purity 97%+In StockPharmaceutical Standards
CAS No.115960-63-9
Molecular FormulaC20H13Cl2NO2
Molecular Weight370.23 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

6-Chloro-9-(4-chlorophenoxy)-2-methoxyacridine CAS 115960-63-9 chemical structure

Description

The molecular framework of 6-Chloro-9-(4-chlorophenoxy)-2-methoxyacridine (C20H13Cl2NO2) is characterized by a steroid core, an amide group, a hydroxyl group, an ether linkage, chlorine substitution. In reversed-phase chromatography, its retention is governed primarily by its high hydrophobicity (logP), which provides a practical basis for HPLC-UV/DAD or LC-MS method development. The high carbon-to-hydrogen ratio imparts good lipophilicity, allowing liquid-liquid extraction with non-polar solvents such as n-hexane or ethyl acetate.

CATO supplies 6-Chloro-9-(4-chlorophenoxy)-2-methoxyacridine (CAS 115960-63-9), a certified reference material (molecular formula C20H13Cl2NO2, MW 370.23 g/mol) for analytical method development and quality control.

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

CATO manufactures 6-Chloro-9-(4-chlorophenoxy)-2-methoxyacridine under ISO 17034:2016 accreditation with dual CNAS and ANAB accreditation. Each batch is characterized by orthogonal methods and supplied with a full Certificate of Analysis (COA), ensuring metrological traceability.

Physical & Chemical Properties

Molecular FormulaC20H13Cl2NO2
Molecular Weight370.23 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 chloroform, dichloromethane, ethyl acetate, DMSO
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light; Contains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)14.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1990
Halogen ContentCl-containing
Nitrogen Atoms1

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