2,2-Di([1,1'-biphenyl]-4-yl)-1-phenylethanone CAS 71482-15-0

Purity 97%+In StockPharmaceutical Standards
CAS No.71482-15-0
Molecular FormulaC32H24O
Molecular Weight424.53 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

2,2-Di([1,1'-biphenyl]-4-yl)-1-phenylethanone CAS 71482-15-0 chemical structure

Description

The occurrence of 2,2-Di([1,1'-biphenyl]-4-yl)-1-phenylethanone is closely related to a hydroxyl group, an ether linkage, a polycyclic aromatic system in its molecular formula, which determines its behaviour during synthesis, purification, or degradation.

CATO supplies 2,2-Di([1,1'-biphenyl]-4-yl)-1-phenylethanone (CAS 71482-15-0), a certified reference material (molecular formula C32H24O, MW 424.53 g/mol) for analytical method development and quality control.

2,2-Di([1,1'-biphenyl]-4-yl)-1-phenylethanone (C32H24O) contains a hydroxyl group, an ether linkage, a polycyclic aromatic system. Its high carbon-to-hydrogen ratio confers good lipid solubility; these physicochemical properties determine the optimal preparation and storage of its standard solutions. The high carbon-to-hydrogen ratio imparts good lipophilicity, allowing liquid-liquid extraction with non-polar solvents such as n-hexane or ethyl acetate.

Recommended for analytical method development and validation; each product is supplied with a full Certificate of Analysis (COA) ensuring ISO 17034 metrological traceability.

CATO manufactures 2,2-Di([1,1'-biphenyl]-4-yl)-1-phenylethanone 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 FormulaC32H24O
Molecular Weight424.53 g/mol
AppearancePale yellow to yellow crystalline powder
Purity97%+
StorageStore at room temperature, protect from light
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
StabilityLight-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)21.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1977

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