1-Methylimidazole, >98%

Price range: $92.70 through $378.86

Product Code: KI-0017-HP

CAS NO: 616-47-7

  • Chemical Formula: C4H6N2
  • Synonyms: MIM, MeIM, 1-Methyl-1H-imidazole,ย N-Methylimidazole, NMI, NMIz

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SUM Formula: C4H6N2

Molecular Weight: 82.10

Purity: >98%

  • SUM Formula: C4H6N2
  • Molecular Weight: 82.10

1-Methylimidazole, CAS: 616-47-7

Key Applications:

Thermodynamics and Solution Chemistry

  • Serves as a model heterocycle for studying protonation equilibria, pKa shifts, and temperatureโ€‘dependent acidโ€“base behavior in aqueous media.
  • Used in thermodynamic investigations of hydrogenโ€‘bonding networks, solvation energies, and enthalpy/entropy contributions in mixed solvent systems.
  • Supports research on ionโ€“dipole interactions and activity coefficients, enabling calibration of predictive models for electrolyte and nonโ€‘electrolyte solutions.
  • Functions as a benchmark compound for evaluating temperatureโ€‘dependent partitioning, vaporโ€“liquid equilibria, and aqueousโ€“organic phase behavior.

Catalysis and Synthesis

  • Acts as a mild, selective nucleophilic catalyst in acylation, esterification, and carbonylโ€‘activation reactions.
  • Used as a base and ligand in organometallic transformations, including transitionโ€‘metalโ€‘mediated coupling and activation pathways.
  • Supports synthesis of ionic liquids, imidazolium salts, and functionalized heterocycles through Nโ€‘alkylation and quaternization.

Polymer and Materials Chemistry

  • Employed as a curing accelerator in epoxy and polyurethane systems, improving crosslinking kinetics and thermal stability.
  • Used as a precursor or modifier in designing imidazoleโ€‘functional polymers with tunable hydrophilicity and ionโ€‘transport properties.
  • Contributes to studies of polymerโ€“solvent interactions, particularly in waterโ€‘rich environments where imidazoleโ€“water hydrogen bonding influences swelling and diffusion.

Analytical and Biochemical Applications

  • Serves as a reference compound for NMR, UVโ€‘Vis, and conductivity studies involving heterocyclic bases in aqueous solutions.
  • Used in biochemical buffer development where imidazoleโ€‘based proton donors/acceptors are required for pHโ€‘sensitive assays.
  • Supports mechanistic studies of enzymeโ€‘mimetic catalysis, especially those involving histidineโ€‘like proton shuttling.

Electrochemistry and Energy

  • Investigated as a protonโ€‘conducting additive in aqueous and mixedโ€‘solvent electrolytes.
  • Used to probe electrode interfacial thermodynamics, including adsorption, charge transfer, and solvation structure.
  • Contributes to formulation studies for aqueous batteries, supercapacitors, and fuelโ€‘cell membranes where imidazoleโ€“water interactions influence conductivity.

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Additional information

Weight 25 g
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