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HS Code |
674035 |
| Chemical Name | 1-Cyanopropyl-3-methylimidazolium tetrafluoroborate |
| Cas Number | 822616-38-8 |
| Molecular Formula | C8H12BF4N3 |
| Molecular Weight | 237.01 g/mol |
| Appearance | Colorless to pale yellow liquid |
| Melting Point | - |
| Boiling Point | - |
| Density | 1.23 g/cm3 (approximate) |
| Solubility In Water | Miscible |
| Purity | Typically >98% |
| Storage Temperature | Room temperature |
| Canonical Smiles | C[n+]1ccn(C)1CCC#N.[BF4-] |
| Synonyms | CPMIM BF4 |
| Hazard Statements | May cause skin and eye irritation |
| Application | Ionic liquid, used in chemical synthesis and catalysis |
As an accredited 1-Cyanopropyle-3-Methylimidazolium Tetrafluoroborate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 250g of 1-Cyanopropyl-3-methylimidazolium tetrafluoroborate packaged in an amber glass bottle with a secure, chemical-resistant screw cap. |
| Shipping | 1-Cyanopropyl-3-methylimidazolium tetrafluoroborate is shipped in tightly sealed containers, protected from moisture and air. It is transported as a chemical substance under standard regulations, requiring proper labeling and documentation. Handle with care, storing at room temperature and avoiding exposure to incompatible materials. Use personal protective equipment during handling and transport. |
| Storage | 1-Cyanopropyl-3-methylimidazolium tetrafluoroborate should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from moisture, heat, and direct sunlight. Avoid contact with strong oxidizing agents. Store under inert atmosphere if possible to prevent hydrolysis or decomposition. Use appropriate personal protective equipment when handling. Keep container upright and clearly labeled to ensure safety. |
Applications of 1-Cyanopropyl-3-Methylimidazolium Tetrafluoroborate in Industrial Manufacturing1-Cyanopropyl-3-Methylimidazolium Tetrafluoroborate (CPMIM BF4) is a stable ionic liquid with key advantages in electrochemistry, specialty separations, pharmaceutical synthesis, and catalysis. As a chemical raw material manufacturer, we supply CPMIM BF4 for quality-driven downstream producers seeking advanced functional properties in process intensification, efficiency, and compliance. 1. Electrolytes for High-Performance SupercapacitorsSupercapacitor and energy storage manufacturers use CPMIM BF4 as a non-volatile, thermally stable electrolyte in high capacitance cells. The ionic liquid increases voltage windows and enhances ionic conductivity compared to traditional aqueous or organic solvents. Stable cycling and resistance to oxidation unlock higher device reliability for industrial and automotive energy module production. Direct integration in cell filling lines requires strict moisture and contaminant control, supported by downstream quality lab monitoring. Industry compliance standards
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2. Electroplating and Metal Surface TreatmentCPMIM BF4 serves as an eco-friendly ionic liquid component in modern metal finishing baths, particularly for aluminum and light alloy electroplating. It provides a stable, non-aqueous medium that enables uniform deposition rates, reduces dendritic growth, and enhances surface smoothness. Downstream users achieve tightly controlled layer thickness, minimal hydrogen evolution, and improved corrosion resistance. Process engineers value the material’s low vapor pressure, which allows safer and more consistent operation in closed plating lines. Industry compliance standards
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3. Solvent for Advanced Organometallic SynthesisSpecialty and pharmaceutical chemical manufacturers employ CPMIM BF4 as a polar, aprotic solvent for organometallic and transition metal-catalyzed reactions. Its high chemical and thermal stability allows safe operation at elevated temperatures during multi-step synthesis. The low vapor pressure ensures minimal loss during long reactor runs. The material supports green chemistry routes by reducing the requirement for volatile organic solvents. Downstream manufacturers benefit from improved selectivity and increased catalyst recyclability. Industry compliance standards
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4. Gas Separation and Capture MediaIndustrial gas separation plants utilize CPMIM BF4 in the design of absorption media for selective removal of carbon dioxide, SOx, and NOx from mixed gas streams. Its high chemical affinity for acid gases enables more energy-efficient scrubbing cycles. Process engineers combine CPMIM BF4 with supporting ionic liquids or add-molecular sieves to improve selectivity and loading. The low volatility reduces solvent loss in continuous operation. Proper material handling and monitoring ensure sustained cyclic performance over extended process campaigns. Industry compliance standards
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5. Reaction Medium for Homogeneous Catalytic HydrogenationChemical producers select CPMIM BF4 as a non-protic reaction medium in homogeneous catalytic hydrogenation processes involving olefins, ketones, and pharmaceutical precursors. Its ionic nature stabilizes catalytic species and inhibits unwanted side reactions, supporting higher selectivity for target products. The thermal and chemical inertness also allow safe operation under high pressure. Downstream users install solvent monitors to manage quality, and employ phase-separation techniques to recover and reuse the ionic liquid at scale. Industry compliance standards
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Producing 1-Cyanopropyl-3-Methylimidazolium Tetrafluoroborate means getting to know the quirks, habits, and fine points of ionic liquids. At our facility, workers handle each synthesis step directly, checking every batch to spot a finish that’s off or a color that seems strange. The human nose still catches some impurities before instruments do. Over the years, changes in stirrer speed, temperature, or raw material sequence have changed not only the efficiency of reactions but also downstream purity. This chemical, abbreviated as [C3CNmim][BF4], walks a line between selective solvency and resistance to hydrolysis, setting it apart from more famous room-temperature ionic liquids.
Manufacturing starts with a sharp focus on raw materials. High-purity 1-methylimidazole and 1-bromopropionitrile combine before purification by repeated washings. Each summer brings shifts in yield because environmental humidity plays tricks with crystallization. Bringing the product to the tetrafluoroborate stage involves patient step-downs in temperature and careful control over water content. Any excess moisture risks hydrolysis, which ruins the yield and worsens conductance in later electrochemical work. Temperature curves tracked and archived during each run give a practical guide for operators, far more reliable than manufacturer’s theory ever could.
Instead of flooding clients with long tables, we keep a focus on what matters: key impurities, color, and handling profile. The typical batch arrives as a clear, almost colorless viscous liquid. If ambient storage conditions tip above 35°C, viscosity can shift, but the core ionic character resists breakdown. We maintain water content below 50 ppm through rigorous vacuum-drying, because years of customer feedback tied trace water to side reactions in metal-catalyzed syntheses, especially in labs running high-precision electrodeposition or ligand screening.
Density and refractive index, routinely measured by our QC staff, rarely drift from batch to batch, because raw feedstock traceability and fixed process controls remain embedded in daily practice. Acidic or basic degradation products signal shortcuts during washings, shortcuts we learned to root out after early customers reported shelf-life reductions back in 2017.
1-Cyanopropyl-3-Methylimidazolium Tetrafluoroborate stands out most in catalytic and synthetic schemes demanding both high polarity and chemical robustness. Over the last ten years, our partners in organometallic synthesis—who once struggled with solvent coordination messing up selectivity—have leaned on this ionic liquid to solubilize both metals and polar reagents. The presence of the cyanopropyl side chain gives an edge in dissolving nitrile, amine, or halide-functionalized solutes. As one veteran process chemist from Germany put it, “You get a workhorse ionic liquid that won’t hydrolyze your boronic acids or eat at sensitive catalysts.”
Battery developers—particularly those exploring safer non-aqueous electrolytes—asked us about ionic liquids which would reduce dendrite growth or oxidative side reactions. The tetrafluoroborate anion manages a practical balance. It stays inert under moderate voltage without the aggressive reactivity seen in hexafluorophosphate or perchlorate variants. Cycling tests run at our pilot-scale plant, where real-world contamination is impossible to avoid, demonstrated that the [BF4]- anion stays stable across weeks of repeated lithium intercalation and stripping. The cyanopropyl chain interacts differently with salt additives, shifting solubilities to fine-tune battery performance in partnership with our customers’ R&D leaders.
Other users, especially in biomass fractionation and cellulose dissolution, rely on the subtle solvent power of [C3CNmim][BF4]. Chromatography-based labs sometimes receive product residues with faint yellowing—evidence of trace thermal degradation. From these episodes, we learned to accelerate post-reaction cooling and improve airtight packaging, minimizing oxygen ingress during shipping.
Ionic liquid supply can be a wild field. Many companies churn out close analogs like 1-butyl-3-methylimidazolium tetrafluoroborate ([Bmim][BF4]), but the jump to a cyanopropyl chain brings a shift in solvating abilities and chemical resilience. We learned early that even a swing from a butyl to a cyanopropyl group changes everything from miscibility to toxicity profile. Safety testing indicated that [C3CNmim][BF4] emits lower vapor pressures under heat, and repeated exposure studies show the nitrile tail modifies absorption compared to standard alkyl imidazoliums. This affects workplace safety guidelines and scales of operation, especially for clients planning to move from beaker batches to tonnage scale production.
Chemists working with transition metals notice improved selectivity due to the less coordinating nature of the cyanopropyl group. A researcher from a leading Japanese fine chemicals company shared that moving from [Bmim][BF4] to [C3CNmim][BF4] cut their side-product formation in cross-coupling reactions by nearly 20%. We changed our technical guidance after seeing this repeated outcome across client applications. Where butyl-based versions tend to show minor decomposition in strong base, the cyanopropyl holds up with notable stability. This has a real impact on yield and disposal requirements, which we see reflected in repeat orders from process chemists demanding consistency.
Solubility for gases also shifts. We document in our own records that [C3CNmim][BF4] uptakes CO2 about 10% faster than the butyl analog in real temperature-pressure sweeps. Several large industrial partners working on gas separations and capture pilot plants now specify our product due in part to this observed advantage. The implications reach all the way into process design, since equipment can run at slightly lower pressures, reducing energy use. This originated not from theory, but from hands-on process feedback and troubleshooting on customer sites.
Years of pilot and kilolab production built habits into our staff. They wash the reaction vessels between runs with extra care—trace residues from previous batches have shown up as contamination peaks in NMR spectra, which careful QC first flagged when a respected university lab sent back unusual spectral data. Rather than ignoring these “outliers,” we invested in more thorough cleaning routines and batch-to-batch documentation. Line supervisors still keep paper logs alongside digital records, cross-checking odd smells, colors, or viscosity changes, because some knowledge can’t be captured on a screen.
On the packaging side, practical improvements followed directly from complaints and advice. A northern European lab once reported leaky cap liners that let the product absorb humidity during shipping. Instead of switching logistics vendors, we redesigned seals for better hermetic closure and triple-checked drying protocols. This way, the shipped product has a measurable reduction in contaminant levels, which lowers the risk of interference in high-sensitivity analytical methods at the customer site.
Every operator in our plant trains on the specifics of ionic liquid hazards, since [C3CNmim][BF4] sets off some false negatives on standard halide leak detectors. We rely on dedicated trace fluoride monitors, and regular air sampling spots leaks earlier than standard practice. The result is not just safer working conditions, but a sharper product profile without background halide odor, an improvement we first registered in 2019 after shifting our maintenance schedule.
Over the last decade, we watched the growing use of [C3CNmim][BF4] as a response to tightening green chemistry demands in multiple sectors. In synthetic chemistry, the push away from volatile solvents led clients to comb through the options for room-temperature ionic liquids that could sustain difficult catalytic cycles without generating side products. As feedback returned from field labs, we added more rigorous hydrolysis testing and invested in better headspace analyzers to identify volatile trace products that might impact product shelf life.
Environmental and sustainability teams across the specialty chemicals and energy industries expect not just data but preparedness for regulatory change. Regulators in Asia and Europe have asked for toxicity and environmental fate data extending beyond what standard tests provide. We engage directly with these agencies, repeating test runs and updating SDS documents to reflect each adjustment, rather than running on autopilot. Feedback about product toxicity led to stricter handling advice and new purity benchmarks.
Clients stepping up from R&D to pilot or commercial deployment often ask for advice on solvent recycling and system cleanout. Our technical service engineers get into the nuts and bolts of system compatibility, supporting customers in choosing compatible gaskets and tubing that perform well with [C3CNmim][BF4]. Many learned the hard way that elastomers compatible with standard alkyl-imidazolium salts sometimes resist swelling less successfully here. A plant in the American Midwest recently reported that switching elastomer grades cut downtime during solvent change-out by 15%, a savings that quickly justified a higher up-front engineering investment. Stories like these shape our own product guidance and technical bulletins.
Every year brings new requirements from chemists and manufacturers—cleaner product, sharper analysis, less environmental impact, better cost. We keep the line open with our collaborators for honest criticism and clear requests. For example, clients in advanced materials frequently look for modified versions of [C3CNmim][BF4] with higher thermal stability or alternative anions tailored for specific reactivity. Our R&D team actively tackles these projects with what we learn in production and feedback, never losing sight of the lessons learned in scale-up or the little surprises in each new application.
We remember the early years when shifts in ionic liquid market demand made pricing unpredictable. We invested in localizing some raw material sourcing, reducing transportation time and lessening storage risk, especially during the pandemic’s logistics upheaval. These practical moves absorbed some market shocks and helped to guarantee our clients product supply at more consistent pricing—even as base chemical costs fluctuated. These experiences reinforce the value of stable processes and transparent communication between manufacturer, supplier, and end user.
Each customer working with 1-Cyanopropyl-3-Methylimidazolium Tetrafluoroborate brings a unique set of challenges, from electrode stability to optimum evaporation conditions. Researchers sometimes discover surprising new uses—such as flow battery electrolytes or CO2 capture technology—by repurposing this ionic liquid beyond its intended role. Our production and technical support teams share best practices and troubleshooting notes, often connecting researchers who would never otherwise know each other’s work. These professional relationships—formed at the manufacturing and quality control level—feed innovation back upstream.
Looking back over our own records, hundreds of performance reports and technical bulletins trace back to operator logs, small modifications, and written notes made on the plant floor. These cumulative changes make the product more reliable, less variable, and more likely to meet the needs of demanding users across the world. We see ourselves as stewards of this practical knowledge pool, handing down practices to the next shift and next generation of chemists and technicians.
Change starts small, with tweaks in the washing process, a tighter drying curve, or a new packaging seal. Feedback from a specialty chemical plant in Brazil led us to improve trace metal analysis, because product color shifts made them nervous about downstream purity. By working directly with their staff and sharing chromatography results, we removed a persistent contaminant in subsequent runs, earning customer confidence and more business in the process. Everyone on the production line now understands why these quality checks matter—not in theory, but through practical result and customer impact.
No shortcuts exist for reliable ionic liquid manufacturing. Success grows from routine, shared wisdom, and accountability, reinforced by decades in the business. By continually listening, revising, and incorporating new insights with openness, we keep our product at the leading edge of performance for applications that stretch from academic research labs to the floors of industrial plants worldwide.