[4-(but-3-en-1-yl)phenyl]boronic acid CAS 226422-89-5

Purity 97%+In StockPharmaceutical Standards
CAS No.226422-89-5
Molecular FormulaC10H13BO2
Molecular Weight176.02 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

[4-(but-3-en-1-yl)phenyl]boronic acid CAS 226422-89-5 chemical structure

Description

The assigned purity is verified by mass-balance and quantitative NMR (qNMR) approaches, with the expanded uncertainty reported at a 95% confidence level (k=2). Batch homogeneity and stability are independently assessed for every lot.

CATO supplies [4-(but-3-en-1-yl)phenyl]boronic acid (CAS 226422-89-5), a certified reference material (molecular formula C10H13BO2, MW 176.02 g/mol) for analytical method development and quality control.

[4-(but-3-en-1-yl)phenyl]boronic acid (C10H13BO2) contains a carboxylic acid group, a hydroxyl group, an ether linkage, an aromatic ring system. Its high carbon-to-hydrogen ratio confers good lipid solubility, the carboxyl group imparts weak acidity; these physicochemical properties determine the optimal preparation and storage of its standard solutions. The aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

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.

Physical & Chemical Properties

Molecular FormulaC10H13BO2
Molecular Weight176.02 g/mol
AppearanceOff-white to pale yellow crystalline powder
Purity97%+
StorageStore at 2-8°C
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
StabilityMay oxidize slowly on prolonged air exposure
Degree of Unsaturation (DBE)4.5
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)2021

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