Stable isotope labeling allows researchers to study metabolic pathways in vivo in a safe manner.
Stable isotope-labeled compounds are used as environmental pollutant standards for the detection of air, water, soil, sediment and food.
In addition to treating various diseases, isotopes are used for imaging, diagnosis, and newborn screening.
Small molecule compounds labeled with stable isotopes can be used as chemical reference for chemical identification, qualitative, quantitative, detection, etc. Various types of NMR solvents can be used to study the structure, reaction mechanism and reaction kinetics of compounds.
Stable isotope labeling allows researchers to study metabolic pathways in vivo in a safe manner.
Stable isotope-labeled compounds are used as environmental pollutant standards for the detection of air, water, soil, sediment and food.
General Information |
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Catalog: BLP-008610 |
Molecular Formula: [13C]6H7BO2 |
Molecular Weight: 127.89 |
Chemical Structure |
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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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