1-Hexyl-2-methylimidazole, >98%

Price range: $248.39 through $2,486.37

Product Code: KI-0011-HP

CAS NO: 82410-68-2

  • Chemical Formula: C10H18N2
  • Synonyms: 1-Hex-2-MIM, 1-Hexyl-2-methyl-1 H-imidazole
  • SMILES: CCCCCCN1C=CN=C1C.

 

 

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SUM Formula: C10H18N2

Molecular Weight: 166.26

Purity: >98%

  • SPECIFIC GRAVITY: NA
  • SUM Formula: C10H18N2
  • Molecular Weight: 166.26
  • TSCA: NA

1-Hexyl-2-methylimidazole, CAS: 82410-68-2

Key Applications:

1. Precursor and Intermediate in Ionic Liquid Synthesis

  • Serves as an alkylated imidazole building block for preparing hydrophobic ionic liquids with long‑chain cations.
  • Useful for generating salts with bis(trifluoromethylsulfonyl)imide (TFSI), PF₆⁻, BF₄⁻, and other anions for electrochemical and materials applications.
  • Enables tuning of viscosity, polarity, and thermal stability in task‑specific ionic liquids.

2. Corrosion Inhibition and Surface Protection

  • Long alkyl chain improves adsorption on metal surfaces, making it a candidate for corrosion‑inhibitor formulations in acidic or chloride‑rich environments.
  • Can be blended with other heterocyclic inhibitors to enhance film‑forming behavior.

3. Phase‑Transfer and Catalytic Applications

  • Acts as a nucleophilic base or ligand in organic synthesis, particularly in alkylation, substitution, and condensation reactions.
  • The hydrophobic C6 chain improves compatibility with nonpolar media, enabling biphasic or solvent‑free catalytic systems.

4. Surfactant and Amphiphilic Additive

  • Amphiphilic structure supports micelle formation and interfacial modification.
  • Can be incorporated into formulations requiring controlled wetting, dispersion, or stabilization.

5. Electrolyte and Additive in Energy‑Related Systems

  • Serves as a precursor for cationic species used in electrolytes for batteries, supercapacitors, and electrochemical devices.
  • The imidazole core contributes to ionic conductivity, while the hexyl chain enhances hydrophobicity and thermal robustness.

6. Polymer and Material Modification

  • Functions as a reactive monomer or chain‑transfer component in specialty polymer systems.
  • Can be grafted onto polymer backbones to introduce ionic or amphiphilic character, improving adhesion, flexibility, or chemical resistance.

7. Coordination and Organometallic Chemistry

  • Nitrogen donor site enables coordination to transition metals, supporting catalyst development or mechanistic studies.
  • Useful in designing metal–organic frameworks (MOFs) or functionalized ligands with tailored solubility.

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Additional information

Weight 25 g
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