6,7-Diphenyl-3H-pyrrolizin-3-one CAS 105508-08-5

Purity 97%+In StockPharmaceutical Standards
CAS No.105508-08-5
Molecular FormulaC19H13NO
Molecular Weight271.31 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

6,7-Diphenyl-3H-pyrrolizin-3-one CAS 105508-08-5 chemical structure

Description

The occurrence of 6,7-Diphenyl-3H-pyrrolizin-3-one is closely related to a steroid core, an amide group, a hydroxyl group, an ether linkage in its molecular formula, which determines its behaviour during synthesis, purification, or degradation.

CATO supplies 6,7-Diphenyl-3H-pyrrolizin-3-one (CAS 105508-08-5), a certified reference material (molecular formula C19H13NO, MW 271.31 g/mol) for analytical method development and quality control.

6,7-Diphenyl-3H-pyrrolizin-3-one (C19H13NO) contains a steroid core, an amide group, a hydroxyl group, an ether linkage. Its high carbon-to-hydrogen ratio confers good lipid solubility; these physicochemical properties determine the optimal preparation and storage of its standard solutions. 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), 6,7-Diphenyl-3H-pyrrolizin-3-one 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 FormulaC19H13NO
Molecular Weight271.31 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
StabilityLight-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)14.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1987
Nitrogen Atoms1

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