(2-Phenyl-1,3,2-dioxaborolan-4-yl)methanol CAS 2412-76-2

Purity 97%+In StockPharmaceutical Standards
CAS No.2412-76-2
Molecular FormulaC9H11BO3
Molecular Weight177.99 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

(2-Phenyl-1,3,2-dioxaborolan-4-yl)methanol CAS 2412-76-2 chemical structure

Description

CATO supplies (2-Phenyl-1,3,2-dioxaborolan-4-yl)methanol (CAS 2412-76-2), a certified reference material (molecular formula C9H11BO3, MW 177.99 g/mol) for analytical method development and quality control.

The molecular framework of (2-Phenyl-1,3,2-dioxaborolan-4-yl)methanol (C9H11BO3) 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 the polarity and ionization state of its functional groups, which provides a practical basis for HPLC-UV/DAD or LC-MS method development. 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).

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

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.

Physical & Chemical Properties

Molecular FormulaC9H11BO3
Molecular Weight177.99 g/mol
AppearanceOff-white to pale yellow crystalline powder
Purity97%+
StorageStore at 2-8°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.)1957

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