4,4,5,5-Tetramethyl-2-(7-phenylnaphthalen-2-yl)-1,3,2-dioxaborolane CAS 2226451-93-8

Purity 97%+In StockPharmaceutical Standards
CAS No.2226451-93-8
Molecular FormulaC22H23BO2
Molecular Weight330.23 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

4,4,5,5-Tetramethyl-2-(7-phenylnaphthalen-2-yl)-1,3,2-dioxaborolane CAS 2226451-93-8 chemical structure

Description

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 supplies 4,4,5,5-Tetramethyl-2-(7-phenylnaphthalen-2-yl)-1,3,2-dioxaborolane (CAS 2226451-93-8), a certified reference material (molecular formula C22H23BO2, MW 330.23 g/mol) for analytical method development and quality control.

The molecular framework of 4,4,5,5-Tetramethyl-2-(7-phenylnaphthalen-2-yl)-1,3,2-dioxaborolane (C22H23BO2) is characterized by a steroid core, a hydroxyl group, an ether linkage. 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. The aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

CATO manufactures 4,4,5,5-Tetramethyl-2-(7-phenylnaphthalen-2-yl)-1,3,2-dioxaborolane 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 FormulaC22H23BO2
Molecular Weight330.23 g/mol
AppearancePale yellow to yellow crystalline powder
Purity97%+
StorageStore at 2-8°C, protect from light
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)11.5
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1998

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