3,4-Dimethylphenyl 1,2,3,4-tetrahydroacridine-9-carboxylate CAS 853317-79-0

Purity 97%+In StockPharmaceutical Standards
CAS No.853317-79-0
Molecular FormulaC22H21NO2
Molecular Weight331.41 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

3,4-Dimethylphenyl 1,2,3,4-tetrahydroacridine-9-carboxylate CAS 853317-79-0 chemical structure

Description

CATO manufactures 3,4-Dimethylphenyl 1,2,3,4-tetrahydroacridine-9-carboxylate 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.

3,4-Dimethylphenyl 1,2,3,4-tetrahydroacridine-9-carboxylate (CAS 853317-79-0) is a high-purity analytical reference standard with the molecular formula C22H21NO2 and a molecular weight of 331.41 g/mol.

The molecular framework of 3,4-Dimethylphenyl 1,2,3,4-tetrahydroacridine-9-carboxylate (C22H21NO2) is characterized by a steroid core, an amide group, a hydroxyl group, an ether linkage. 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 presence of an aromatic ring or conjugated system gives the compound characteristic absorption bands in the UV-Vis region, making it well suited to UV or diode-array detection (DAD).

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 FormulaC22H21NO2
Molecular Weight331.41 g/mol
AppearancePale yellow to yellow crystalline powder
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
Degree of Unsaturation (DBE)13.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1987
Nitrogen Atoms1

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