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N-Methylpyrrole-[d4]

General Information
Catalog: BLP-012014
CAS: 190386-37-9
Molecular Formula: C5H3D4N
Molecular Weight: 85.14
Chemical Structure
N-Methylpyrrole-[d4]
Synonyms N-Methylpyrrole-d4 (ring-d4); 1H-Pyrrole-2,3,4,5-d4, 1-methyl-(9ci)
IUPAC Name 2,3,4,5-tetradeuterio-1-methylpyrrole
Related CAS 96-54-8 (unlabelled)
Canonical SMILES CN1C=CC=C1
InChI InChI=1S/C5H7N/c1-6-4-2-3-5-6/h2-5H,1H3/i2D,3D,4D,5D
InChI Key OXHNLMTVIGZXSG-QFFDRWTDSA-N
Boiling Point 112.499°C at 760 mmHg
Purity 99% atom D
Density 0.908 g/cm3
Solubility Soluble in Acetone, Chloroform, Methanol
Appearance Yellow to Dark Yellow Oil
Storage Store at -20°C

N-Methylpyrrole-[d4], a deuterated compound utilized in a myriad of scientific research applications, particularly in spectroscopy and analytical chemistry. Here are key applications of N-Methylpyrrole-[d4] depicted with a high degree of perplexity and burstiness:

NMR Spectroscopy: A staple in Nuclear Magnetic Resonance (NMR) spectroscopy, N-Methylpyrrole-[d4] serves as an internal standard, invaluable for molecular analysis. The deuterium atoms within this compound yield distinct signals from standard hydrogen, facilitating the differentiation and examination of hydrogen-containing compounds within mixtures. Researchers leverage this property to precisely decipher the structure and dynamics of organic molecules, unraveling intricate molecular mysteries.

Pharmaceutical Research: In the realm of pharmaceutical exploration, N-Methylpyrrole-[d4] emerges as a pivotal tracer molecule with immense utility. By incorporating deuterium-labeled drug candidates, researchers delve into the in vivo study of drug metabolism and pharmacokinetics with unparalleled precision. This knowledge is paramount in comprehending the journey of a drug within the body, from absorption to distribution, metabolism, and excretion, shedding light on crucial pharmacological insights.

Chemical Synthesis: An indispensable reagent in organic synthesis, N-Methylpyrrole-[d4] stands as a catalyst for innovation in chemical entity development. Deuterium's presence exerts influence on reaction mechanisms and outcomes, enabling chemists to explore isotope effects on reaction pathways. This exploration can unveil novel synthetic routes and optimize reaction conditions, propelling chemical synthesis into new realms of discovery.

Environmental Analysis: In the domain of environmental chemistry, N-Methylpyrrole-[d4] assumes the role of an isotopic tracer synonymous with illuminating pathways of environmental pollutants. Deuterated compounds play a crucial role in tracking the fate of chemical substances across various environmental matrices such as soil and water. These studies are imperative for assessing the environmental implications and behavior of contaminants, safeguarding environmental health and sustainability.

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