Paroxetine 4-Hydroxy Metabolite CAS 112058-90-9

Purity >95%In StockPharmaceutical Standards
CAS No.112058-90-9
Molecular FormulaC19H22FNO3
Molecular Weight331.38 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

Paroxetine 4-Hydroxy Metabolite CAS 112058-90-9 chemical structure

Description

As a certified reference material (CRM), Paroxetine 4-Hydroxy Metabolite 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.

Paroxetine 4-Hydroxy Metabolite (CAS 112058-90-9) is a high-purity analytical reference standard with the molecular formula C19H22FNO3 and a molecular weight of 331.38 g/mol.

The molecular framework of Paroxetine 4-Hydroxy Metabolite (C19H22FNO3) is characterized by a steroid core, an amide group, a hydroxyl group, an ether linkage, fluorine 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. Halogen substitution (F/Cl/Br/I) produces a distinctive isotope pattern in mass spectrometry, a valuable aid for qualitative confirmation.

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 FormulaC19H22FNO3
Molecular Weight331.38 g/mol
AppearancePale yellow to yellow crystalline powder. (slight halide-like odor)
Purity>95%
StorageStore at 2-8°C, protect from light, keep sealed and dry
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)9.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1989
Halogen ContentF-containing
Nitrogen Atoms1

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