4,4,5,5-Tetramethyl-2-phenyl-1,3,2-dioxaborolane CAS 24388-23-6

Purity >95%In StockPharmaceutical Standards
CAS No.24388-23-6
Molecular FormulaC12H17BO2
Molecular Weight204.07 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

4,4,5,5-Tetramethyl-2-phenyl-1,3,2-dioxaborolane CAS 24388-23-6 chemical structure

Description

Compared with other compounds in its class, the molecular weight of 204.07 g/mol gives 4,4,5,5-Tetramethyl-2-phenyl-1,3,2-dioxaborolane distinctive chromatographic separation conditions and mass-spectrometry parameter settings.

4,4,5,5-Tetramethyl-2-phenyl-1,3,2-dioxaborolane (CAS 24388-23-6) is a high-purity analytical reference standard with the molecular formula C12H17BO2 and a molecular weight of 204.07 g/mol.

Owing to a carboxylic acid group, a hydroxyl group, an ether linkage, an aromatic ring system, 4,4,5,5-Tetramethyl-2-phenyl-1,3,2-dioxaborolane is typically off-white to pale yellow crystalline powder. Its solid-state physicochemical attributes — including a molecular weight of 204.07 g/mol — guide the selection of appropriate sample preparation and analytical techniques. The aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

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

As a certified reference material (CRM), 4,4,5,5-Tetramethyl-2-phenyl-1,3,2-dioxaborolane 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 FormulaC12H17BO2
Molecular Weight204.07 g/mol
AppearanceOff-white to pale yellow crystalline powder
Purity>95%
StorageStore at room temperature
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.)1963

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