1-Ethyl-2,3-dimethylimidazolium tetrafluoroborate, >98%

Price range: $220.76 through $12,471.65

Product Code: IL-0001-HP

CAS NO: 307492-75-7

  • Chemical Formula: C7H13BF4N2
  • Synonyms: EDiMIM BF4, Im112 BF4
  • Anion decomposes slowly in the presence of water.
  • Aromatic

Clear

SUM Formula: C7H13BF4N2

Molecular Weight: 212.00

Melting Point: 104 °C

Density: 1.21 g/cm³

Purity: >98%

  • SUM Formula: C7H13BF4N2
  • Molecular Weight: 212.00
  • Melting Point: 104 °C
  • Density: 1.21 g/cm³

1-Ethyl-2,3-dimethylimidazolium tetrafluoroborate, CAS: 307492-75-7

Key Applications:

1. Electrochemical Systems

  • Electrolytes for supercapacitors and batteries

The 2,3‑dimethyl substitution increases cation rigidity and reduces ring acidity, improving electrochemical stability windows. Paired with BF₄⁻, it supports high ionic conductivity and moderate hydrophobicity, making it suitable for double‑layer capacitors and certain non‑aqueous battery chemistries.

  • Electrodeposition media

The ionic liquid can dissolve metal salts and support smooth, uniform electrodeposition of metals such as Cu, Ni, and Ag under water‑free conditions.

2. Catalysis and Reaction Media

  • Solvent for Lewis‑acid‑catalyzed transformations

BF₄⁻ can weakly coordinate to metal centers, enabling catalytic systems for alkylation, isomerization, and Friedel–Crafts‑type reactions.

  • Medium for organometallic catalysis

The steric bulk around the imidazolium ring reduces unwanted side reactions (e.g., carbene formation), making it a stable medium for Pd, Ru, and Ir catalysts.

  • Biphasic catalysis

Its density and immiscibility with some organic solvents allow phase‑separable reaction systems.

3. Separation and Extraction

  • Selective extraction of metal ions

BF₄⁻‑based ionic liquids can extract transition‑metal complexes, especially when paired with chelating ligands.

  • Gas absorption and separation

Although not as strong as fluorosulfonyl or NTf₂⁻ systems, [EMMIm][BF₄] can absorb SO₂, H₂S, and CO₂ to a moderate extent, useful for screening studies or tunable solvent systems.

4. Materials Processing

  • Polymerization media

The ionic liquid can act as a solvent or co‑solvent for radical and cationic polymerizations, improving control over molecular weight distribution.

  • Nanomaterial synthesis

Its ionic environment stabilizes nanoparticles (Au, Pt, Fe₃O₄) and can influence particle size and morphology.

5. Spectroscopy and Analytical Chemistry

  • Matrix or solvent for electrochemical and spectroscopic studies

Low volatility and good conductivity make it suitable for cyclic voltammetry, impedance spectroscopy, and NMR studies of reactive intermediates.

  • Sample preparation

Useful in dispersive liquid–liquid microextraction (DLLME) for hydrophobic analytes.

6. General Solvent and Process Uses

  • Non‑volatile replacement for traditional organic solvents

Its stability and low vapor pressure support use in high‑temperature or closed‑system processes.

  • Ionic‑liquid‑based lubricants and additives

BF₄⁻ systems can reduce friction and wear in metal–metal interfaces, though NTf₂⁻ salts are more common.

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1-Ethyl-2,3-dimethylimidazolium tetrafluoroborate (CAS: 307492-75-7) is an imidazolium-based ionic liquid developed for research and industrial applications in electrochemistry and materials science. This compound combines a 1-ethyl-2,3-dimethylimidazolium cation with a tetrafluoroborate anion. Supplied at a purity of >98%, it is a white to off-white crystalline solid at room temperature and becomes a liquid upon heating.

Properties:

Property Value
CAS Number 307492-75-7
Molecular Formula C₇H₁₃BF₄N₂
Molecular Weight 212.00 g/mol
Purity >98%
Melting Point 104 °C
Density 1.21 g/cm³ (at 25 °C)
Viscosity Not Available
Electrochemical Window Not Available

Handling and Storage:

  • Moisture Sensitivity: Store and handle under dry conditions to avoid hydrolysis of the tetrafluoroborate anion.
  • Storage Conditions: Keep in a tightly sealed container at 15–25 °C, in a dry, well-ventilated place away from moisture and direct sunlight.
  • Safety Precautions: Always handle with gloves, safety glasses, and a lab coat. Consult the Safety Data Sheet (SDS) for comprehensive safety guidelines.

Additional information

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