5-Nitro-1H-imidazole-1-ethanol-d4

Product Name 5-Nitro-1H-imidazole-1-ethanol-d4
CAT No. CS-T-83112
CAS No. 1794791-19-7
Category Stable Isotopes
Stock Enquire
Mol. Wt. Not Available
Mol. For. Not Available
Hazardous This is not a Hazardous Compound
COA View Sample COA
MSDS View Sample MSDS
Smileys [2H]C(N1C=NC=C1[N+]([O-])=O)([2H])C(O)([2H])[2H]
Canonical Smiles C1=C(N(C=N1)CCO)[N+](=O)[O-]
InchIKey DFMZECOLZRIPOT-LNLMKGTHSA-N
Inchl InChI=1S/C5H7N3O3/c9-2-1-7-4-6-3-5(7)8(10)11/h3-4,9H,1-2H2/i1D2,2D2
IUPAC 1,1,2,2-tetradeuterio-2-(5-nitroimidazol-1-yl)ethanol
Controlled No
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5-Nitro-1H-imidazole-1-ethanol-d4 is a deuterated derivative of 5-Nitro-1H-imidazole-1-ethanol, which is a nitroimidazole compound that has been extensively used as a potent antimicrobial agent against anaerobic bacteria, protozoa, and helminths. The deuterated form of this compound is often used in research and drug development as a stable isotope-labeled internal standard in mass spectrometry-based quantitative analyses. The chemical formula of 5-Nitro-1H-imidazole-1-ethanol-d4 is C4D4N3O3, and its molecular weight is 157.14 g/mol. The compound is synthesized by replacing the hydrogen atoms on the deuterium atoms on the imidazole ring and the hydroxyl group. It is a white to pale-yellow crystalline powder that is soluble in water and methanol. In addition to its role as an internal standard, 5-Nitro-1H-imidazole-1-ethanol-d4 has also been used in studies investigating the pharmacokinetics and metabolism of nitroimidazole drugs, including its parent compound. It has been shown to exhibit similar pharmacological properties as the non-deuterated compound and has been used as a surrogate for metabolic studies. Overall, 5-Nitro-1H-imidazole-1-ethanol-d4 is a valuable tool in the development of new antimicrobial agents and the study of the pharmacokinetics and metabolism of nitroimidazole drugs.

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