1-Heptyl-3-methylimidazolium bromide, >99%

Price range: $190.97 through $8,124.78

Product Code: IL-0298-HP

CAS NO: 343851-32-1

  • Chemical Formula: C11H21BrN2
  • Synonyms: HeptMIM Br, C1C7Im Br, Im17 Br
  • Aromatic
Clear

SUM Formula: C11H21BrN2

Molecular Weight: 261.20

Melting Point: <RT

Purity: >99%

Viscosity: 6680 cP (25 °C)

  • SUM Formula: C11H21BrN2
  • Molecular Weight: 261.20
  • Melting Point:
  • Viscosity: 6680 cP (25 °C)

1-Heptyl-3-methylimidazolium bromide, CAS: 343851-32-1

Key Applications:

Solvent & Reaction Medium

  • Serves as a tunable ionic liquid solvent for organic synthesis, benefiting from moderate hydrophobicity and strong ionic character.
  • Enhances reaction rates and selectivity in acid‑catalyzed, transition‑metal‑catalyzed, and nucleophilic substitution reactions.
  • Useful in biphasic catalysis where partial immiscibility with water supports efficient product separation.

Electrochemical & Energy Applications

  • Functions as an electrolyte component or ionic additive in electrochemical systems, including supercapacitors and electrodeposition baths.
  • Improves ionic conductivity and electrode interface stability due to the imidazolium cation’s charge transport efficiency.
  • Supports electrodeposition of metals such as copper, nickel, and silver under low‑volatility, thermally stable conditions.

Surfactant, Micelle, and Self‑Assembly Systems

  • Exhibits amphiphilic behavior suitable for forming micelles, vesicles, and structured phases in aqueous and mixed‑solvent systems.
  • Applied in colloid stabilization, nanoparticle templating, and controlled‑size nanomaterial synthesis.
  • Useful in studying ionic‑liquid‑based surfactant systems due to its intermediate alkyl chain length (C7), which tunes critical micelle concentration and aggregation behavior.

Extraction, Separation & Purification

  • Effective in liquid–liquid extraction of metal ions, dyes, and organic contaminants.
  • Bromide counterion supports halide‑assisted extraction mechanisms and coordination with metal complexes.
  • Applied in separation of aromatic compounds, phenolics, and bioactive molecules through hydrophobic and π–π interactions.

Biomolecular & Materials Processing

  • Used as a stabilizing medium for enzymes and proteins in non‑aqueous or mixed‑solvent environments.
  • Supports dissolution and processing of biopolymers such as cellulose and chitin when paired with co‑solvents.
  • Enables fabrication of ionic‑liquid‑modified polymers, membranes, and thin films with enhanced conductivity and mechanical properties.

Nanomaterials & Catalysis

  • Acts as a templating or stabilizing agent in the synthesis of metal nanoparticles, metal oxides, and carbon nanostructures.
  • Enhances dispersion and prevents aggregation due to strong electrostatic and steric stabilization.
  • Serves as a medium for catalytic transformations requiring controlled microenvironments.

Please contact us if you want to learn more or need assistance with your order.

Additional information

Weight 25 g
Qty

, , , , , ,