1-Cyanopropyl-3-Methylimidazolium Tetrafluoroborate: Detailed Insights

What Is 1-Cyanopropyl-3-Methylimidazolium Tetrafluoroborate?

1-Cyanopropyl-3-methylimidazolium tetrafluoroborate stands out as a representative ionic liquid built on an imidazolium backbone, carrying a cyanopropyl functional group and paired with a tetrafluoroborate anion. The chemical formula comes out to C8H12BF4N3, which arranges itself into a two-part structure, with the positive ion providing both chemical stability and tunable reactivity, while the BF4- anion lends the material unique solubility and phase properties. This compound often appears in forms like a clear to pale yellow liquid, fine flakes, or a crystalline powder depending on ambient temperature and purity, all sharing a reputation for handling moisture and air without breaking down quickly. By design, the structure brings together organic and inorganic features, opening a path for wide applications, from solvents and electrolytes through to materials processing and catalysis. The HS Code usually referenced runs under 2942000000, fitting its place as an organic/heterocyclic compound within standard trade classifications.

Key Properties and Physical Characteristics

Weighing in with a molecular weight hovering around 259.0 g/mol, this material doesn’t float off or evaporate the way ordinary organics do. Its density measures about 1.2-1.3 g/cm3 close to room temperature, a sign of the close-packed ions and a real testament to the amount of matter per liter one can expect. In my work with specialty solvents, this characteristic means a small volume holds significant chemical punch—a feature valued in precision synthesis. The melting point usually sits in the range where it switches from solid flakes to a clear and viscous liquid between 40-65°C, depending on sample purity and moisture. Unlike many classic organic salts, the tetrafluoroborate anion keeps the material stable against sudden hydrolysis and common acids, supporting use in both research labs and manufacturing plants.

Molecular Structure and Reactivity

Within the structure, the imidazolium ring connects to a methyl group and a 1-cyanopropyl chain. This arrangement brings in polar and nonpolar territories, allowing interaction with diverse chemical environments. Such flexibility expands what scientists can achieve: dissolving stubborn reagents, offering catalytic power, or supporting ionic conduction without the danger of fire or rapid evaporation present in traditional solvents. The tetrafluoroborate element acts as a stabilizer, controlling the electrical environment of the molecule. Because ionic liquids like this one avoid volatility and flammability, labs can use them in setups where safety is critical—like battery research, electroplating, and even in nanomaterial processing.

Physical Forms and Typical Presentation

Commercially, 1-cyanopropyl-3-methylimidazolium tetrafluoroborate arrives as solid powder, pearl-like beads, fine flakes, clear to slightly yellow solutions, or, with precise moisture control, as large faceted crystals. Each form serves a role: powders and flakes ease measurement and blending, while liquids deliver convenience in synthesis. In my experience, storing the material in tightly sealed glass or HDPE containers limits water uptake, keeping properties consistent, which matters for anyone relying on predictable reaction outcomes. Depending on supplier and storage, users may find the compound slightly viscous, hinting at its ionic nature and the cohesion among molecules.

Specification Details

Technical sheets provide specifications on purity, water content, acidity, and color, because each plays a part in the final application. High purity (99% and above) assures minimal interference, especially crucial in pharmaceutical and electronic ingredient manufacturing. Water content below 0.5% tends to support best performance, as excess moisture can disrupt both solubility and reactivity. Keeping acidity low secures compatibility with sensitive reagents, such as organometallics, that may break down if too much acid lingers in the raw material. From experience, strict batch-to-batch checks avoid product drift over time—a reality any producer faces as operations scale up and batch sizes change.

Safety, Hazards, and Environmental Considerations

Handling any chemical brings its challenges, and this ionic liquid asks for respect like so many industrial substances. The cyanopropyl group signals potential toxicity if ingested or absorbed, so gloves and goggles stay mandatory. Extended use in closed or poorly ventilated areas can raise concerns about slow vapor accumulation—small, but never a worry to ignore out of habit. Spill response needs absorbent material, with disposal routed through chemical waste containers rather than routine drains. Experience confirms the importance of keeping the salt away from strong acids, oxidizers, or high heat, since byproducts could result that change both toxicity and flammability.

Regarding environmental risks, the lack of volatility drastically cuts down on air emissions, but the stability of the tetrafluoroborate anion means wastewater removal requires specialist handling. For research labs or factories, established waste management practices need an update to accommodate these persistent ionic residues. In the push for greener chemistry, manufacturers look for recycling systems to limit raw material losses—recovering and purifying the compound for reuse saves both money and downstream impact, a practice already seeing adoption among specialty chemical makers.

Raw Materials and Upstream Supply

Sourcing the starting ingredients connects back to basic organics and mineral fluorides. Methylimidazole joins with 3-chloropropionitrile to build the cation; sodium tetrafluoroborate then swaps in the BF4 unit through a salt metathesis reaction. The purity and sustainability of these raw materials affect the end product’s quality and environmental outcome. As regulations on hazardous chemicals tighten, supply chains for such fluorinated compounds must become more traceable. The industry gradually shifts to cleaner synthesis, both for regulatory peace-of-mind and to attract customers demanding accountability in what goes into their labs or devices.

Practical Importance and Solutions

Experience shows that understanding both the nature and challenges of 1-cyanopropyl-3-methylimidazolium tetrafluoroborate sets the stage for safe and successful use. In electrochemistry work, the material’s conductivity and electrochemical stability make new battery technologies possible, while its solvency solves real-world headaches in organic synthesis. Yet the journey doesn’t end at purchase—safe storage, controlled use, reliable disposal, and material recovery all factor into responsible handling. By focusing on these aspects, chemical managers and researchers keep risks in check and advance toward greener, safer lab and factory work. The movement toward closed-loop systems and supplier traceability grows year by year, hinting at a future where advanced chemicals like this one support progress without leaving environmental debt behind.