5-Chloro-1-methyl-4-nitroimidazole-13C4

Product Name 5-Chloro-1-methyl-4-nitroimidazole-13C4
CAT No. CS-T-72889
CAS No. 1391052-79-1
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 CN1C=NC(=C1Cl)[N+](=O)[O-]
Canonical Smiles CN1C=NC(=C1Cl)[N+](=O)[O-]
InchIKey OSJUNMSWBBOTQU-JCDJMFQYSA-N
Inchl InChI=1S/C4H4ClN3O2/c1-7-2-6-4(3(7)5)8(9)10/h2H,1H3/i1+1,2+1,3+1,4+1
IUPAC 5-chloro-1-(113C)methyl-4-nitro(2,4,5-13C3)imidazole
Controlled No
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5-Chloro-1-methyl-4-nitroimidazole-13C4 (also known as [13C4]-Chloramphenicol) is a stable isotope-labeled analog of Chloramphenicol, which is a broad-spectrum antibiotic used to treat bacterial infections. The 13C4 labeling allows for the tracking of the compound in biological systems and pharmacokinetic studies. The chemical formula of [13C4]-Chloramphenicol is C11H7ClN4O3, with a molecular weight of 290.66 g/mol. The compound is a yellow crystalline powder and has a melting point of 155-159 °C. It is soluble in ethanol and methanol, but insoluble in water. [13C4]-Chloramphenicol is used in research studies to investigate its pharmacokinetics, efficacy, and toxicity in animal and human models. It is also used as an internal standard in mass spectrometry analysis of Chloramphenicol in biological samples. The compound works by inhibiting bacterial protein synthesis, specifically by binding to the 50S ribosomal subunit and preventing the formation of peptide bonds. This results in the inhibition of bacterial growth and the treatment of bacterial infections. However, [13C4]-Chloramphenicol should only be used for research purposes and not for human or animal consumption due to its potential toxicity and adverse effects. It is important to handle the compound with caution and follow proper safety protocols.

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