1-Hexyl-2,3-dimethylimidazolium iodide, >98%

Price range: $206.54 through $9,033.43

Product Code: IL-0138-HP

CAS NO: 288627-94-1

  • Chemical Formula: C11H21IN2
  • Synonyms: HDiMIM I, C1C1C6Im I, Im116 I
  • Light sensitive
  • Aromatic
Clear

SUM Formula: C11H21IN2

Molecular Weight: 308.07

Melting Point: 79 °C

Density: 0.666 g/cm³ (25 °C)

Purity: >98%

  • SUM Formula: C11H21IN2
  • Molecular Weight: 308.07
  • Melting Point: 79 °C
  • Density: 0.666 g/cm³ (25 °C)

1-Hexyl-2,3-dimethylimidazolium iodide, CAS: 288627-94-1

Key Applications

Solvent and Reaction Medium

  • Functions as a hydrophobic ionic liquid suitable for biphasic and phase‑transfer–driven transformations.
  • Supports nucleophilic substitution, alkylation, and metal‑catalyzed reactions where iodide enhances substrate activation.
  • Useful in moisture‑sensitive or low‑volatility process environments due to its thermal stability and negligible vapor pressure.

Electrochemical and Redox Systems

  • Serves as an iodide‑based electrolyte component for redox‑active systems, including dye‑sensitized solar cells (DSSCs) and photoelectrochemical devices.
  • Enhances charge transport in systems requiring high iodide concentration and stable cation–anion pairing.
  • Suitable for electrodeposition baths where iodide improves metal‑ion complexation and deposition uniformity.

Materials Processing and Thin‑Film Fabrication

  • Acts as a templating or structure‑directing ionic liquid for polymeric, inorganic, or hybrid materials.
  • Supports controlled crystallization and morphology tuning in halide‑sensitive materials.
  • Useful in perovskite precursor formulations where iodide availability influences film quality and defect passivation.

Catalysis and Phase‑Transfer Enhancement

  • Provides iodide as a strong nucleophile for catalytic cycles requiring halide exchange or activation.
  • Facilitates organocatalytic and metal‑mediated transformations by stabilizing reactive intermediates.
  • Effective in biphasic catalysis where the long C6 chain improves partitioning and mass transfer.

Extraction, Separation, and Partitioning

  • Enables selective extraction of metal ions, organohalides, and iodine‑containing species through tunable hydrophobicity.
  • Supports liquid–liquid extraction systems where iodide enhances complex formation or redox‑driven separations.
  • Useful in analytical workflows requiring halide‑rich ionic phases.

Antisolvent and Crystallization Control

  • Provides a controlled ionic environment for crystallizing organic salts, pharmaceuticals, and coordination compounds.
  • The iodide anion can modulate polymorph formation and solubility behavior in halide‑sensitive systems.

Polymer and Composite Formulations

  • Functions as a plasticizing or conductivity‑enhancing additive in ion‑conducting polymers.
  • Supports the formation of ionogels and hybrid electrolytes where iodide mobility is required.

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Additional information

Weight 25 g
Qty

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