3,5-Dicarboxyphenylboronic Acid Pinacol Ester CAS 1041434-13-2

Purity 97%+In StockPharmaceutical Standards
CAS No.1041434-13-2
Molecular FormulaC14H17BO6
Molecular Weight292.09 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

3,5-Dicarboxyphenylboronic Acid Pinacol Ester CAS 1041434-13-2 chemical structure

Description

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

3,5-Dicarboxyphenylboronic Acid Pinacol Ester (CAS 1041434-13-2) is a high-purity analytical reference standard with the molecular formula C14H17BO6 and a molecular weight of 292.09 g/mol.

3,5-Dicarboxyphenylboronic Acid Pinacol Ester (C14H17BO6) contains a carboxylic acid group, a hydroxyl group, an ether linkage, an aromatic ring system. It is notably hygroscopic, the carboxyl group imparts weak acidity; these physicochemical properties determine the optimal preparation and storage of its standard solutions. 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).

CATO manufactures 3,5-Dicarboxyphenylboronic Acid Pinacol Ester 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 FormulaC14H17BO6
Molecular Weight292.09 g/mol
AppearanceOff-white to pale yellow crystalline powder
Purity97%+
StorageStore at 2-8°C, protect from light, keep sealed and dry
Solubility (reference)Soluble in methanol, acetonitrile, DMSO, water (slightly soluble)
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light; Hygroscopic; reseal immediately after opening
Degree of Unsaturation (DBE)6.5
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1988

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