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Oxalic Acid-[d2]

General Information
Catalog: BLP-012050
CAS: 2065-73-8
Molecular Formula: C2D2O4
Molecular Weight: 92.5
Chemical Structure
Oxalic Acid-[d2]
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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