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Phenylboronic Acid-[13C6]

General Information
Catalog: BLP-008610
Molecular Formula: [13C]6H7BO2
Molecular Weight: 127.89
Chemical Structure
Phenylboronic Acid-[13C6]
Description Phenylboronic Acid-[13C6] is an isotope labelled compound of Phenylboronic Acid. Phenylboronic Acid is a compound used in organic synthesis of various pharmaceutical goods.
Synonyms B-Phenylboronic Acid-13C6; Dihydroxyphenylborane-13C6; Phenylboric Acid-13C6; Phenylboronic Acid-13C6; Phenyldihydroxyborane-13C6
Related CAS 98-80-6 (unlabelled)
Melting Point 207-210°C
Purity 98% by CP; 98% atom 13C
Solubility Slightly soluble in Methanol, Chloroform
Appearance Off-white Solid
Storage Store at -20°C

Phenylboronic Acid-[13C6], a stable isotopically labeled compound, is a versatile tool with extensive applications in chemical and biochemical research. Here are key applications of Phenylboronic Acid-[13C6] presented with high perplexity and burstiness:

NMR Spectroscopy: Immersing into the intricate world of nuclear magnetic resonance (NMR) spectroscopy, Phenylboronic Acid-[13C6] emerges as a fundamental element in unraveling molecular structures and dynamics. The isotope carbon-13 introduces heightened sensitivity and resolution in spectra, offering researchers intricate insights into chemical environments. This indispensable tool sheds light on the complexities of both organic and biomolecular structures, providing a microscopic glimpse into the unseen.

Biomedical Research: Venturing into the realm of biomedical research, Phenylboronic Acid-[13C6] shines as a beacon in metabolic studies and drug development. Its unique isotopic signature acts as a guiding star, tracing the metabolic fate of boronic acid-containing drugs and natural compounds within biological systems. This knowledge forms the foundation for informed decisions on pharmacokinetics and therapeutic efficacy, heralding a new era of personalized medicine.

Synthetic Chemistry: Within the domain of synthetic organic chemistry, Phenylboronic Acid-[13C6] emerges as a versatile cornerstone for building blocks and reagents. The distinctive boronic acid functionality opens doors to cross-coupling reactions, crucial for creating novel carbon-carbon bonds. The isotopic label enriches mechanistic studies, empowering chemists to navigate reaction pathways with precision and finesse, thereby elevating synthesis processes to new heights of sophistication.

Sensor Development: Pioneering the frontier of sensor technology, Phenylboronic Acid-[13C6] takes the spotlight in crafting sensitive detectors for saccharides and other analytes. Its unique interactions with diol-containing molecules lay the groundwork for boronic acid-based sensors with diverse applications, including glucose monitoring. The carbon-13 label brings additional analytical prowess to the table, enabling precise quantitative analyses in complex matrices, propelling sensor technology towards unprecedented levels of accuracy and reliability.

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