4-Carboethoxy-3-(3-pyrrolinomethyl) benzophenone CAS 898789-87-2

Purity 97%+In StockPharmaceutical Standards
CAS No.898789-87-2
Molecular FormulaC21H21NO3
Molecular Weight335.40 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

4-Carboethoxy-3-(3-pyrrolinomethyl) benzophenone CAS 898789-87-2 chemical structure

Description

Based on its molecular formula C21H21NO3, 4-Carboethoxy-3-(3-pyrrolinomethyl) benzophenone contains a steroid core, an amide group, a hydroxyl group, an ether linkage; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 335.40 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. 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 4-Carboethoxy-3-(3-pyrrolinomethyl) benzophenone (CAS 898789-87-2), a certified reference material (molecular formula C21H21NO3, MW 335.40 g/mol) for analytical method development and quality control.

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.

CATO manufactures 4-Carboethoxy-3-(3-pyrrolinomethyl) benzophenone 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 FormulaC21H21NO3
Molecular Weight335.40 g/mol
AppearancePale yellow to yellow crystalline powder
Purity97%+
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
Degree of Unsaturation (DBE)12.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1987
Nitrogen Atoms1

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