3,3-Dimethyl-2,4-dihydro-1,5-benzodioxepine-6-boronic acid CAS 2096341-50-1

Purity 97%+In StockPharmaceutical Standards
CAS No.2096341-50-1
Molecular FormulaC11H15BO4
Molecular Weight222.05 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

3,3-Dimethyl-2,4-dihydro-1,5-benzodioxepine-6-boronic acid CAS 2096341-50-1 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 3,3-Dimethyl-2,4-dihydro-1,5-benzodioxepine-6-boronic acid (CAS 2096341-50-1), a certified reference material (molecular formula C11H15BO4, MW 222.05 g/mol) for analytical method development and quality control.

The molecular framework of 3,3-Dimethyl-2,4-dihydro-1,5-benzodioxepine-6-boronic acid (C11H15BO4) is characterized by a carboxylic acid group, a hydroxyl group, an ether linkage, an aromatic ring system. 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 high carbon-to-hydrogen ratio imparts good lipophilicity, allowing liquid-liquid extraction with non-polar solvents such as n-hexane or ethyl acetate.

As a certified reference material (CRM), 3,3-Dimethyl-2,4-dihydro-1,5-benzodioxepine-6-boronic acid 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 FormulaC11H15BO4
Molecular Weight222.05 g/mol
AppearanceOff-white to pale yellow crystalline powder
Purity97%+
StorageStore in a cool place (≤25°C), keep sealed and dry
Solubility (reference)Soluble in methanol, ethanol, DMSO
StabilityMay oxidize slowly on prolonged air exposure; Hygroscopic; reseal immediately after opening
Degree of Unsaturation (DBE)4.5
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1997

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