1-Methyl-3-propylimidazolium tetrafluoroborate, >98%

Price range: $121.62 through $6,971.12

Product Code: IL-0143-HP

CAS NO: 244193-48-4

  • Chemical Formula: C7H13BF4N2
  • Synonyms: PMIM BF4, C1C3Im BF4, Im13 BF4
  • Anion decomposes slowly in the presence of water
  • Hydrophilic
  • Aromatic
Clear

Conductivity: 4.080 mS/cm

SUM Formula: C7H13BF4N2

Molecular Weight: 212.0

Melting Point: -47 °C

Density: 1.27 g/cm³ (20 °C)

Purity: >98%

Viscosity: 74.4 cP (25 °C)

  • SUM Formula: C7H13BF4N2
  • Molecular Weight: 212.0
  • Melting Point: -47 °C
  • Density: 1.27 g/cm³ (20 °C)
  • Viscosity: 74.4 cP (25 °C)

1-Methyl-3-propylimidazolium tetrafluoroborate, CAS: 244193-48-4

Key Applications:

Solvent and Electrolyte Functions

  • Serves as a low‑volatility, thermally stable solvent for organic synthesis, particularly in substitution, cyclization, and transition‑metal‑catalyzed reactions.
  • Functions as an electrolyte component in electrochemical systems requiring moderate viscosity and stable ionic conductivity.
  • Supports electrodeposition studies where BF₄⁻ anions promote smooth metal film formation and minimize passivation.

Catalysis and Reaction Media

  • Provides a tunable, non‑aqueous medium for acid‑catalyzed transformations, including esterifications and alkylations.
  • Enhances selectivity in biphasic and phase‑transfer systems due to its balanced polarity and miscibility profile.
  • Useful in microwave‑assisted synthesis, where ionic liquids accelerate heating and improve reaction efficiency.

Separation and Extraction

  • Employed in liquid–liquid extraction of aromatic hydrocarbons, phenolics, and metal ions, leveraging BF₄⁻’s relatively weak coordinating behavior.
  • Supports chromatographic method development as an additive or stationary‑phase modifier to improve peak shape and analyte retention control.

Materials and Polymer Science

  • Acts as a plasticizing and conductivity‑enhancing additive in polymer electrolytes, ion gels, and composite membranes.
  • Used in templating and dispersion of nanoparticles, where the imidazolium cation stabilizes metal or metal‑oxide surfaces.
  • Facilitates the preparation of hybrid materials requiring ionic domains for charge transport or structural tuning.

Spectroscopy and Analytical Chemistry

  • Provides a stable, low‑volatility matrix for spectroscopic studies of solvation, ion pairing, and reaction intermediates.
  • Serves as a calibration or reference medium in electroanalytical experiments due to its predictable ionic mobility.

Energy and Environmental Applications

  • Investigated as a component in redox‑flow and dye‑sensitized solar cell electrolytes where BF₄⁻ offers oxidative stability.
  • Supports CO₂ capture and gas‑solubility studies, particularly in systems evaluating cation structure–property relationships.

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Additional information

Weight 25 g
Qty

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