3-Phenyl-1,2,3,4,9,10-hexahydroacridine-1,9-dione CAS 188015-78-3

Purity 97%+In StockPharmaceutical Standards
CAS No.188015-78-3
Molecular FormulaC19H15NO2
Molecular Weight289.33 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

3-Phenyl-1,2,3,4,9,10-hexahydroacridine-1,9-dione CAS 188015-78-3 chemical structure

Description

CATO supplies 3-Phenyl-1,2,3,4,9,10-hexahydroacridine-1,9-dione (CAS 188015-78-3), a certified reference material (molecular formula C19H15NO2, MW 289.33 g/mol) for analytical method development and quality control.

Owing to a steroid core, an amide group, a hydroxyl group, an ether linkage, 3-Phenyl-1,2,3,4,9,10-hexahydroacridine-1,9-dione is typically pale yellow to yellow crystalline powder. Its solid-state physicochemical attributes — including a molecular weight of 289.33 g/mol — guide the selection of appropriate sample preparation and analytical techniques. 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.

As a certified reference material (CRM), 3-Phenyl-1,2,3,4,9,10-hexahydroacridine-1,9-dione meets the metrological traceability requirements of ISO/IEC 17025 laboratories. Batch-to-batch consistency is monitored via control charts to guarantee comparable assigned values across lots.

Physical & Chemical Properties

Molecular FormulaC19H15NO2
Molecular Weight289.33 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.)2010
Nitrogen Atoms1

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