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1-Butyl-3-Methylimidazolium Tetrafluoroborate

    • Product Name 1-Butyl-3-Methylimidazolium Tetrafluoroborate
    • Alias BMIM BF4
    • Einecs 425-420-4
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    Specifications

    HS Code

    183511

    Product Name 1-Butyl-3-Methylimidazolium Tetrafluoroborate
    Cas Number 174501-65-6
    Molecular Formula C8H15BF4N2
    Molecular Weight 226.02 g/mol
    Appearance colorless to pale yellow liquid
    Melting Point -80 °C
    Boiling Point Decomposes before boiling
    Density 1.17 g/cm3 (at 20 °C)
    Solubility In Water miscible
    Purity typically ≥98%
    Ec Number 695-566-3
    Refractive Index 1.425 (at 20 °C)
    Flash Point >120 °C (closed cup)
    Chemical Class Ionic liquid
    Odor characteristic, mild

    As an accredited 1-Butyl-3-Methylimidazolium Tetrafluoroborate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing A 500 mL amber glass bottle with a secure screw cap, labeled "1-Butyl-3-Methylimidazolium Tetrafluoroborate, CAS 174501-65-6."
    Shipping 1-Butyl-3-Methylimidazolium Tetrafluoroborate is shipped in tightly sealed containers to prevent moisture exposure. It is classified as non-flammable and generally stable, but should be handled as a chemical substance with standard precautions. Packages are clearly labeled, compliant with safety regulations, and shipped with appropriate documentation to ensure safe and legal transport.
    Storage 1-Butyl-3-Methylimidazolium Tetrafluoroborate should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from sources of moisture and incompatible substances such as strong oxidizers. Protect from direct sunlight and ignition sources. Ensure proper labeling and secondary containment to prevent leaks. Store at room temperature, following all safety protocols for handling ionic liquids.
    Application of 1-Butyl-3-Methylimidazolium Tetrafluoroborate

    Purity 99%: 1-Butyl-3-Methylimidazolium Tetrafluoroborate with purity 99% is used in lithium-ion battery electrolytes, where it enhances ionic conductivity and improves cycling stability.

    Viscosity 52 cP: 1-Butyl-3-Methylimidazolium Tetrafluoroborate with viscosity 52 cP is used in electrochemical capacitors, where it ensures efficient charge transport and low internal resistance.

    Thermal Stability up to 300°C: 1-Butyl-3-Methylimidazolium Tetrafluoroborate with thermal stability up to 300°C is used in high-temperature solvent applications, where it maintains solvent integrity and performance under elevated temperatures.

    Moisture Content <0.05%: 1-Butyl-3-Methylimidazolium Tetrafluoroborate with moisture content less than 0.05% is used in the synthesis of air-sensitive organometallic complexes, where it provides anhydrous conditions to prevent undesirable side reactions.

    Conductivity 8.9 mS/cm: 1-Butyl-3-Methylimidazolium Tetrafluoroborate with conductivity 8.9 mS/cm is used in electroplating baths, where it achieves uniform metal deposition and high current efficiency.

    Melting Point -80°C: 1-Butyl-3-Methylimidazolium Tetrafluoroborate with a melting point of -80°C is used as a low-temperature solvent in biomedical devices, where it ensures fluidity and process stability at sub-zero temperatures.

    Density 1.21 g/cm³: 1-Butyl-3-Methylimidazolium Tetrafluoroborate with density 1.21 g/cm³ is used in liquid-liquid extraction of rare earth metals, where it provides selective phase separation and high extraction efficiency.

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    Certification & Compliance
    More Introduction

    Discovering 1-Butyl-3-Methylimidazolium Tetrafluoroborate: A Standout Ionic Liquid

    Unlocking New Doors with 1-Butyl-3-Methylimidazolium Tetrafluoroborate

    Committing to any advanced technology, from energy storage to chemical processing, sparks plenty of questions about materials. My own journey through the world of ionic liquids started in a university lab, hands buried in latex gloves, peering at colorless liquids in glassware. Compared to old-school solvents, new-age materials like 1-butyl-3-methylimidazolium tetrafluoroborate—abbreviated as [BMIM][BF4]—turn heads for reasons that go far beyond chemical curiosity. Not only does this ionic liquid resist easy evaporation, but it also steers clear of the catch-22 “volatile-organic-compound” restrictions that handcuff more traditional options.

    Model Profile and Key Specifications

    A closer look at [BMIM][BF4] reveals qualities that help it stand apart. Each molecule blends a bulky imidazolium core—swapping protons for organic sidechains—with a tetrafluoroborate counter-ion that tames reactivity enough to invite experimentation. Many in research and industry prize this compound for its stable liquid state at room temperature. With a molecular formula of C8H15BF4N2 and a molar mass just north of 226 g/mol, you get a heavy punch for a compact molecule. Purity often exceeds 99 percent, and this level of refinement matters where contaminants sabotage consistency, especially in battery work or precision catalysis.

    You’ll spot [BMIM][BF4] by its clear-to-pale yellow hue and a telltale viscous texture—a feature that pairs well with its low vapor pressure. Handling this material doesn’t challenge experienced chemists; its moderate melting point (just below zero Celsius) sidesteps cold-storage headaches, and the thermal window stretches well above water’s boiling point. The electrochemical stability window easily accommodates high-performance processes in energy storage devices, much wider than what regular organics pull off. The robust ionic conductivity and low flammability build a sense of trust, especially in settings where safety and reliability walk hand in hand.

    Exposure to moist air won’t crumble [BMIM][BF4]—it’ll pick up some water through hygroscopicity, but never with the catastrophic effects seen with, say, lithium aluminum hydride. Used with regular ventilation and standard personal protection, it rarely presents the sort of headaches that cloud other advanced materials. Relying on a trusted certificate of analysis, researchers can focus on results, not hazards.

    Real-World Applications: Where [BMIM][BF4] Shines

    Rolling out a material with such a tailored suite of properties feels like finding a Swiss Army knife in a box of old-fashioned tools. In electrochemistry circles, [BMIM][BF4] regularly acts as the backbone for electrolyte solutions, smoothing out performance in supercapacitors and high-efficiency batteries. Years ago, I saw my own project’s charge-discharge curves leap forward after shifting toward this ionic liquid, thanks mostly to lower resistance and more reliable cycling. Unlike water-based systems, this liquid doesn't boil or degrade under high voltage, giving more freedom to push the envelope on next-generation cells.

    Synthetically, [BMIM][BF4] slices through old bottlenecks in catalysis and separation. Ask a group of synthetic chemists about their solvent headaches, and they’ll often gripe about separations, safety, or cost. This ionic liquid’s low vapor pressure means less worry about fumes in small-scale reactions and industrial runs alike. It dissolves a dizzying range of organic and inorganic compounds, so you get more latitude in process design—with fewer restrictions posed by stubborn reactants or byproducts.

    In my own experience, it handled temperature swings and reactions involving stubborn gas reactants better than many classic dipolar aprotic solvents. I once watched well-separated layers of starting materials dissolve into perfect clarity with [BMIM][BF4], cutting reaction times in half and boosting yields. For metal catalysts, this ionic liquid offers something more: it’s easy to recover precious metals from post-reaction mixtures almost without losses, since the ionic environment encourages leaching and regeneration.

    Lab stories like these add up: [BMIM][BF4] carved paths into green chemistry setups, minimizing the environmental cost. Traditional organic solvents often need expensive, energy-intensive distillation for recycling. In contrast, this ionic liquid rarely evaporates, slashing emissions and letting teams reuse the same batch across projects. That reliability, mixed with easier recovery, keeps both budgets and regulatory headaches in check.

    Extraction companies have jumped on these properties as well. Separation of metal ions from waste streams—especially rare earths and platinum-group metals—leans heavily on ionic liquids. Environmental controls get smoother because [BMIM][BF4] keeps its cool when mixed with acids or organics, pulling out target ions while leaving behind less unwanted waste. The cleaner downstream means companies can pursue tougher clean-up targets without drowning in compliance paperwork.

    Advantages Over Traditional Alternatives

    Debating solvent choices boils down to a handful of priorities: performance, environmental safety, cost, and ease of use. Many traditional organic solvents, such as acetonitrile, dichloromethane, or tetrahydrofuran, come bundled with their own list of tradeoffs. Most lose out on volatility, catching flak for their flammability or quick evaporation. [BMIM][BF4] doesn’t ignite easily, and it won’t vaporize from a glass beaker either. That makes a practical difference in any lab that values air quality—or feels the pinch from fire codes and insurance premiums.

    Water-based alternatives sometimes fill the gap, but those have their own temperature and incompatibility issues. They often fail on stability fronts, especially with reactive organometallics or under strong electric fields. Ionic liquids like [BMIM][BF4] manage tough environments far better because their molecular structure shrugs off harsh reaction conditions. Solubility range, especially when dealing with complex organic or inorganic ions, leaves classic solvents playing catch-up.

    Another edge lies in their non-coordinating nature. Typical polar solvents compete for catalytic sites, changing kinetics or poisoning delicate processes. Switching to [BMIM][BF4], I’ve seen less interference, more predictable rates, and easier isolation of valuable intermediates. The molecular “hands-off” approach unlocks cleaner runs and more trustworthy results.

    Addressing Potential Challenges and Misunderstandings

    The buzz around ionic liquids sometimes eclipses real-world caveats, which any serious operator eventually confronts. [BMIM][BF4] does not solve every problem. Costs, while falling, run higher than bulk solvents. For sprawling chemical plants, these can tip the scales if recovery and reuse systems lag behind. It takes experience to integrate ionic liquids into a production line—routine lab tricks may need rethinking. A few years back, my own group spent weeks refining a protocol for phase separation, only to realize a minor adjustment in pH made all the difference. What seemed like a hurdle led to a better process overall, but only after some hands-on learning.

    Disposal also matters. While low volatility sidesteps emissions, improper dumping of ionic liquids still carries environmental risk. Studies point out that some ionic liquids, including tetrafluoroborate variants, resist biodegradation. This reality has pressed the field toward both greener synthesis routes and stricter waste control. Responsible labs and companies look beyond the sticker price to the full cycle of sourcing, use, and disposal. The most efficient users recover and recycle, closing the loop on the material’s journey and trimming overall impact.

    Emerging Research and Future Outlook

    Momentum gathers as researchers unlock new uses for ionic liquids like [BMIM][BF4]. Sustainable energy draws headlines, and teams working on fuel cells or next-generation electrolyzers increasingly experiment with this material as a high-performance electrolyte. I’ve seen excitement around its ability to support high-voltage chemistries, where water or simple salts falter. The wide electrochemical window stands out, as does the compatibility with both organics and metals. As the push for electrification and renewable storage heats up, these capabilities help meet tougher requirements.

    In catalysis, the versatility of [BMIM][BF4] drives innovation at both bench and industrial scale. More reactions, especially asymmetric syntheses and selectivity-challenged systems, find longer catalyst lifetimes and fewer unwanted byproducts. Inside pharma, where yields and purity spell profit and safety, these improvements have real value. I’ve heard from colleagues who credit ionic liquids for opening new cross-coupling or chiral catalysis doors—moving from theory to practical process within a matter of months.

    Membrane technology and industrial separations—two other fields eager for new solutions—tap [BMIM][BF4] for its ability to tune solubility and permeability. Desalination, carbon dioxide capture, and even specialty gas separation benefit from its unique solvent properties. As the world tightens its goals for cleaner air and water, this versatility helps push old processes in greener directions.

    Interest in additive manufacturing and specialty polymers brings [BMIM][BF4] into unexpected corners. Novel electrochemical deposition, changeable ion conductivity, and enhanced polymer flexibility all trace back to the behavior of the imidazolium backbone and the simple salt counter-ion. Compared to traditional plasticizers and solvents, ionic liquids avoid many of the health and safety traps, while offering more precise property tuning.

    Supporting Safe and Effective Use: Practical Paths Forward

    Safe handling starts with reliable information and strong habits. Material safety data, while often dry reading, helps prevent unexpected mishaps. Where [BMIM][BF4] is concerned, basic chemical hygiene, including gloves and eyewear, lines up well with other familiar laboratory materials. Storage in sealed containers, away from heat and reactive acids, avoids unnecessary breakdown or contamination.

    Tighter safety standards across the industry deserve recognition. I’ve watched labs pivot from trusting old supplier faxes to verifying every new reagent against the latest safety guidance. For ionic liquids, stakeholder groups like American Chemical Society and international toxicology panels generate peer-reviewed guidance to fill knowledge gaps. Regulatory frameworks, especially in Europe and North America, respond as evidence mounts, ensuring application keeps pace with risk management.

    Comparisons with Similar Ionic Liquids

    The family tree of ionic liquids stretches wider every year. [BMIM][BF4] belongs to a set based on imidazolium cations, which have found success due to their flexibility and chemical stability. But related compounds—such as 1-ethyl-3-methylimidazolium tetrafluoroborate ([EMIM][BF4]) or those pairing imidazolium rings with different anions—offer their own performance traits. Swapping butyl for ethyl tweaks melting points and viscosity, which many researchers use to fine-tune behavior for a specific job. Heavier, branched alkyl chains tend to push viscosity higher and, sometimes, raise solubility ceilings for certain solutes.

    Among the counter-ions, switching tetrafluoroborate for hexafluorophosphate or bis(trifluoromethane)sulfonimide shifts the electrochemical window, toxicity, and environmental persistence. BF4- draws praise for a balanced performance-to-toxicity profile, but investigations into its long-term fate in soil and water continue. This spurs innovation: research teams pursue “greener” alternatives, including amino acid-based ionic liquids or other less persistent anions, to keep one step ahead of future regulation.

    One thing stands out from hands-on experience: incremental tweaks can yield major shifts in application. I tested two nearly identical ionic liquids and saw double the conductivity by swapping out just the alkyl chain. This kind of tailoring—made possible because of a deep molecular understanding—places [BMIM][BF4] in a sweet spot for all-purpose work.

    Navigating Evolving Regulation and Standards

    As the field moves forward, experts and newcomers both bump up against an evolving landscape. Environmental agencies, including the EPA and EU ECHA, track new data on compound persistence and toxicity, sometimes outpacing legislative changes. It pays to follow both published findings and draft guidelines. The academic community also plays its part, with conferences and open-source publications sharing real-world impact data. Transparency builds trust; reputations hinge not just on what a product accomplishes, but also on how responsibly users deploy it.

    Certification bodies and industry consortia increasingly audit supply chains for ethical sourcing and best-practice disposal. Buyers placing long-term bets on [BMIM][BF4] factor in not only immediate performance, but also alignment with voluntary environmental, social, and governance goals. That shift benefits everyone, since public trust rests on more than just technical triumphs.

    Community Experience: Peer Perspectives and Shared Lessons

    Collective experience sharpens understanding and drives progress. Conferences, online forums, and trade journals pulse with stories of practical wins and tricky failures. I saw a group of battery researchers transform cell stability by swapping to ionic liquids after months stalled with traditional solvents. Industrial chemists report fewer fires, cleaner workspaces, and less maintenance downtime after integrating [BMIM][BF4]. On the other hand, environmental chemists voice valid concerns about lifecycle impacts, especially where full recovery or neutralization lacks a clear template.

    These discussions carry weight. Direct feedback loops—from bench to boardroom—enable companies, universities, and regulators to revise best practices every year. The spirit of knowledge sharing helps both new and established players steer clear of costly mistakes. Having sat through my share of late-night problem-solving sessions, I can attest: learning from another’s near-miss often beats luck and intuition.

    Pushing the Envelope: What’s Next for [BMIM][BF4]?

    For enthusiasts and skeptics alike, [BMIM][BF4] offers more than another bottle on the chemical shelf. The combination of chemical resilience, safety credentials, and process efficiency has won over many. Those strengths drive new research and commercial moves toward safer, greener, and more adaptable processes across everything from electronics to mining, pharmaceuticals to advanced manufacturing.

    The challenges—stubborn cost, waste management, occasional stubbornness in difficult reactions—are real, but not insurmountable. Partnerships between users, manufacturers, and researchers will keep finding new tricks and tweaks. I've seen firsthand how a tight feedback loop led to a revised workflow, fully closing the material loop and reducing lifetime costs. Each new experiment writes another chapter in the ongoing story, and [BMIM][BF4] consistently features as a versatile, reliable ally in that effort.

    Anyone entering the ionic liquid arena would do well to keep an open mind and a sharp eye on the details. The right preparation, informed by peer insight and regulatory guidance, positions [BMIM][BF4] as a practical, rewarding choice. Not every problem finds its solution in a single molecule, but sometimes, the right tool changes what’s possible—for researchers, industry, and the planet alike.