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Atomfair 5-Methyl-1,10-phenanthroline C13H10N2

Description 5-Methyl-1,10-phenanthroline (CAS No. 3002-78-6) is a high-purity heterocyclic organic compound with the molecular formula C13H10N2. This derivative of 1,10-phenanthroline features a methyl group at the 5-position, enhancing its utility as a chelating ligand and analytical reagent. Ideal for coordination chemistry, catalysis, and material science applications, our product is rigorously tested to ensure ??98% purity (HPLC) and is supplied as a crystalline solid with excellent shelf stability. Suitable for use in metal ion detection, electrochemical studies, and as a building block for advanced molecular architectures. Packaged under inert gas to prevent degradation and available in quantities from milligrams to kilograms…

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Description

Description

5-Methyl-1,10-phenanthroline (CAS No. 3002-78-6) is a high-purity heterocyclic organic compound with the molecular formula C13H10N2. This derivative of 1,10-phenanthroline features a methyl group at the 5-position, enhancing its utility as a chelating ligand and analytical reagent. Ideal for coordination chemistry, catalysis, and material science applications, our product is rigorously tested to ensure ??98% purity (HPLC) and is supplied as a crystalline solid with excellent shelf stability. Suitable for use in metal ion detection, electrochemical studies, and as a building block for advanced molecular architectures. Packaged under inert gas to prevent degradation and available in quantities from milligrams to kilograms to meet both research and industrial-scale demands.

  • CAS No: 3002-78-6
  • Molecular Formula: C13H10N2
  • Molecular Weight: 194.23
  • Exact Mass: 194.084398327
  • Monoisotopic Mass: 194.084398327
  • IUPAC Name: 5-methyl-1,10-phenanthroline
  • SMILES: CC1=CC2=C(C3=C1C=CC=N3)N=CC=C2
  • Synonyms: 5-Methyl-1,10-phenanthroline, 3002-78-6, 1,10-Phenanthroline, 5-methyl-, 5-Methylphenanthroline, NSC 4272

Application

5-Methyl-1,10-phenanthroline is widely employed as a chelating agent for transition metal ions in catalytic systems and spectroscopic analysis. Its modified structure improves solubility and steric tuning in coordination complexes compared to unsubstituted 1,10-phenanthroline. Researchers utilize this compound in the development of luminescent materials, redox-active catalysts, and as a probe for trace metal detection in environmental samples.

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