1-Methylimidazole, >98%
Price range: $92.70 through $378.86
Product Code: KI-0017-HPCAS NO: 616-47-7
- Chemical Formula: C4H6N2
- Synonyms: MIM, MeIM, 1-Methyl-1H-imidazole,ย N-Methylimidazole, NMI, NMIz
To order 5kg or more, please email us at info@roco.global
**This product will incur a $97.00 HazMat fee when the order is placed.**
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 temperatureโdependent acidโbase behavior in aqueous media.
- Used in thermodynamic investigations of hydrogenโbonding networks, solvation energies, and enthalpy/entropy contributions in mixed solvent systems.
- Supports research on ionโdipole interactions and activity coefficients, enabling calibration of predictive models for electrolyte and nonโelectrolyte solutions.
- Functions as a benchmark compound for evaluating temperatureโdependent partitioning, vaporโliquid equilibria, and aqueousโorganic phase behavior.
Catalysis and Synthesis
- Acts as a mild, selective nucleophilic catalyst in acylation, esterification, and carbonylโactivation reactions.
- Used as a base and ligand in organometallic transformations, including transitionโmetalโmediated coupling and activation pathways.
- Supports synthesis of ionic liquids, imidazolium salts, and functionalized heterocycles through Nโalkylation 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 imidazoleโfunctional polymers with tunable hydrophilicity and ionโtransport properties.
- Contributes to studies of polymerโsolvent interactions, particularly in waterโrich environments where imidazoleโwater hydrogen bonding influences swelling and diffusion.
Analytical and Biochemical Applications
- Serves as a reference compound for NMR, UVโVis, and conductivity studies involving heterocyclic bases in aqueous solutions.
- Used in biochemical buffer development where imidazoleโbased proton donors/acceptors are required for pHโsensitive assays.
- Supports mechanistic studies of enzymeโmimetic catalysis, especially those involving histidineโlike proton shuttling.
Electrochemistry and Energy
- Investigated as a protonโconducting additive in aqueous and mixedโsolvent electrolytes.
- Used to probe electrode interfacial thermodynamics, including adsorption, charge transfer, and solvation structure.
- Contributes to formulation studies for aqueous batteries, supercapacitors, and fuelโcell membranes where imidazoleโwater interactions influence conductivity.
Please contact us if you want to learn more or need assistance with your order.




