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-012050 |
CAS: 2065-73-8 |
Molecular Formula: C2D2O4 |
Molecular Weight: 92.5 |
Chemical Structure |
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Synonyms | Oxalic Acid D2; Ethanedioic acid-d2; Oxalic (2H)acid |
IUPAC Name | dideuterio oxalate |
Related CAS | 144-62-7 (unlabelled) |
Isomeric SMILES | [2H]OC(=O)C(=O)O[2H] |
Canonical SMILES | C(=O)(C(=O)O)O |
InChI | InChI=1S/C2H2O4/c3-1(4)2(5)6/h(H,3,4)(H,5,6)/i/hD2 |
InChI Key | MUBZPKHOEPUJKR-ZSJDYOACSA-N |
Boiling Point | 365.1°C at 760 mmHg |
Melting Point | 190 °C (dec.)(lit.) |
Purity | 95% atom D |
Density | 1.772 g/cm3 |
Solubility | Soluble in DMSO, Methanol |
Appearance | White to Off-white Solid |
Storage | Store at -20°C |
Oxalic Acid-[d2], a deuterium-labeled compound, serves as a valuable tool in research settings for exploring diverse chemical and biological processes. Here are key applications of Oxalic Acid-[d2] presented with a high degree of perplexity and burstiness:
Metabolic Tracing: Within the realm of biochemical studies, Oxalic Acid-[d2] emerges as a pivotal tracer for delving into metabolic pathways associated with oxalate metabolism. Researchers can meticulously trace the labeled compound through metabolic reactions, unveiling oxalate's intricate role in physiological processes. This approach enables a deeper comprehension of how oxalate factors into conditions like kidney stones and various metabolic disorders.
NMR Spectroscopy: Employed in Nuclear Magnetic Resonance (NMR) spectroscopy, Oxalic Acid-[d2] facilitates the examination of molecular structure and dynamics. The deuterium labeling plays a crucial role in simplifying NMR spectra by minimizing proton-related complexities, thereby enhancing resolution. This streamlined process empowers scientists to conduct detailed structural analysis and characterization of compounds, pushing the boundaries of molecular investigation.
Environmental Science: Oxalic Acid-[d2] finds its place in environmental science as a tool for dissecting environmental samples, deciphering the fate and movement of oxalates in ecosystems. Through the use of the labeled compound, researchers can meticulously track oxalate's journey and transformations in soils and water bodies. This exploration sheds light on pollution pathways, enriching our understanding of environmental dynamics and fostering efforts in monitoring and remediating environmental issues.
Pharmacokinetics: In the realm of pharmaceutical research, Oxalic Acid-[d2] emerges as a key element in studying the pharmacokinetics and biodistribution of drugs intertwined with oxalate metabolism. Deuterium labeling enables precise monitoring of these metabolic conversions and pathways within biological systems. Such insights play a pivotal role in deciphering drug metabolism, enhancing efficacy assessments, and refining safety profiles, thus contributing to advancements in pharmaceutical sciences.
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