2,4,6-TRis(m-terphenyl-5'-yl)boroxin CAS 909407-14-3

Purity 97%+In StockPharmaceutical Standards
CAS No.909407-14-3
Molecular FormulaC54H39B3O3
Molecular Weight768.32 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

2,4,6-TRis(m-terphenyl-5'-yl)boroxin CAS 909407-14-3 chemical structure

Description

The occurrence of 2,4,6-TRis(m-terphenyl-5'-yl)boroxin is closely related to a carboxylic acid group, 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 2,4,6-TRis(m-terphenyl-5'-yl)boroxin (CAS 909407-14-3), a certified reference material (molecular formula C54H39B3O3, MW 768.32 g/mol) for analytical method development and quality control.

Owing to a carboxylic acid group, a hydroxyl group, an ether linkage, a polycyclic aromatic system, 2,4,6-TRis(m-terphenyl-5'-yl)boroxin is typically pale yellow to yellow amorphous powder. Its solid-state physicochemical attributes — including a molecular weight of 768.32 g/mol — guide the selection of appropriate sample preparation and analytical techniques. The presence of an aromatic ring or conjugated system gives the compound characteristic absorption bands in the UV-Vis region, making it well suited to UV or diode-array detection (DAD).

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 2,4,6-TRis(m-terphenyl-5'-yl)boroxin 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 FormulaC54H39B3O3
Molecular Weight768.32 g/mol
Purity97%+
StorageStore at room temperature, 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)35.5
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1987

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