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HS Code |
800580 |
| Product Name | 1-Octyl-3-Vinylimidazolium Tetrafluoroborate |
| Cas Number | 338739-40-3 |
| Molecular Formula | C15H25BF4N2 |
| Molecular Weight | 320.17 g/mol |
| Appearance | Colorless to pale yellow liquid |
| Density | 1.11 g/cm3 |
| Melting Point | - |
| Boiling Point | - |
| Solubility | Soluble in water and polar organic solvents |
| Ionic Nature | Ionic liquid |
| Purity | Typically ≥98% |
| Refractive Index | 1.477 (approx.) |
| Odor | Odorless |
| Storage Conditions | Store at room temperature, tightly sealed, away from moisture |
As an accredited 1-Octyl-3-Vinylimidazolium Tetrafluoroborate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 250g of 1-Octyl-3-Vinylimidazolium Tetrafluoroborate in a sealed amber glass bottle with tamper-evident cap and chemical hazard labeling. |
| Shipping | **Shipping Description:** 1-Octyl-3-vinylimidazolium tetrafluoroborate is shipped in tightly sealed, chemically resistant containers, protected from moisture and extreme temperatures. The shipment complies with relevant chemical transport regulations. Proper labeling is ensured, and shipping documents include safety and handling instructions. Appropriate cushioning and secondary containment are used to prevent leaks or spills during transit. |
| Storage | 1-Octyl-3-vinylimidazolium tetrafluoroborate should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from moisture and incompatible substances such as strong oxidizers. Protect the chemical from exposure to air and direct sunlight. Use only in areas with appropriate chemical-resistant surfaces and ensure that storage areas are clearly labeled and restricted to trained personnel. |
Applications of 1-Octyl-3-Vinylimidazolium Tetrafluoroborate in Industrial Manufacturing1-Octyl-3-Vinylimidazolium Tetrafluoroborate stands out for its utility in advanced materials processing, electronics, and chemical synthesis. The following application scenarios represent our direct customer base, where the compound delivers key performance advantages for process engineers, formulators, and quality teams in demanding industrial environments. 1. Polymer Electrolyte Development for Solid-State BatteriesThis ionic liquid serves as a functional additive in the polymer electrolyte membranes of lithium and sodium solid-state batteries, supporting ionic conductivity and electrochemical stability across a wide temperature range. Manufacturers introduce the compound during the membrane casting phase to enhance transport properties and suppress dendritic growth, enabling safer, high-performance energy storage solutions. Industry compliance standards
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2. Antistatic Coatings for Flexible Organic ElectronicsOur customers use this ionic liquid as a functional monomer in UV-curable antistatic coatings. Its vinyl group participates in free-radical polymerization, while the imidazolium cation imparts stable ionic conductivity. Applying these coatings on substrates like PET, polycarbonate, and glass ensures static charge dissipation for displays, touch panels, and sensor modules throughout the electronics supply chain. Industry compliance standards
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3. Electrochemical Synthesis as Green Reaction MediaThis ionic liquid facilitates selective organic transformations as a solvent or co-solvent in electrochemical synthesis. Process chemists value its thermal and electrochemical stability for reactions such as anodic coupling or oxidative cyclizations, supporting enhanced yields with improved green metrics compared to conventional solvents. The compound enters the synthesis tank early in the process and directly influences electrolyte properties and product distribution. Industry compliance standards
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4. Ion-Conductive Membranes for Fuel Cell ManufacturingDownstream fuel cell manufacturers incorporate this ionic liquid as a modifier in proton exchange membranes (PEMs) for both low- and high-temperature fuel cell stacks. Its interaction with polymer backbones such as Nafion or polybenzimidazole enhances both proton transfer rates and thermal durability, contributing to improved membrane lifetime under demanding service conditions typical in stationary and mobile fuel cells. Industry compliance standards
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5. Catalytic Support Modification for Heterogeneous CatalystsChemical producers use this material to functionalize silica, alumina, or carbon catalyst supports, creating surface-bound ionic liquid phases for applications in biphasic catalysis. The fast surface polymerization of the vinylimidazolium group ensures a robust ionic environment for immobilized catalyst species, enhancing selectivity and ease of phase separation in reactions such as hydrogenations or alkylations. Industry compliance standards
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6. Additive in Antifouling Marine CoatingsPaint and coatings manufacturers utilize this ionic liquid as a functional additive in antifouling marine coatings, leveraging its ionic conductivity and surface activity. The compound supports the formation of hydrated, slippery layer interfaces that discourage protein and microbial adhesion, especially for vessels, platforms, and marine equipment subject to long-term seawater immersion. It enters the aqueous or solventborne paint formulation during primary mixing and is compatible with acrylic, epoxy, and siloxane systems. Industry compliance standards
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Working directly with ionic liquids on the shop floor and in research labs, you see how each new structure unlocks distinct application pathways. 1-Octyl-3-Vinylimidazolium Tetrafluoroborate (often referred to by its shorthand, [C8VIm][BF4]), doesn’t just offer another name in the catalog—it gives chemists and technologists a real tool for complex tasks. The core of this compound lies in the tuning of both the imidazolium cation and the BF4 anion. We intentionally introduce a vinyl group at the 3-position of the imidazolium ring to provide a functional handle; coupled with an octyl chain attached at the 1-position, this unique arrangement creates a room-temperature ionic liquid with deep practical value.
The model and grade of [C8VIm][BF4] we produce were designed after hundreds of bench-top runs and scale-up campaigns. Genuine material comes free from the haze and excessive halide residue that often plague lesser or hastily made variants. Water content and halide impurity counts matter—serious chemists notice declining performance with impure batches, so our batches test at well below 500 ppm chloride and under 0.2% water by Karl Fischer titration out of the drum. Appearance remains unmistakably clear to slightly pale yellow, liquid at room temperature, never crystallizing out in normal lab settings. We typically offer batches tailored for R&D in 100-gram to multi-liter orders, ensuring minimal batch-to-batch drift and clear lot traceability from reactor to bottle.
Ionic liquids spent a decade as an academic curiosity, but with hands-on synthesis and application, their real strengths stand out. Our [C8VIm][BF4] delivers in areas where other ionic liquids fall short—notably, in catalytic applications, electrochemical devices, and advanced materials processing. Chemists who need to harness the benefits of living radical polymerization look to the vinyl functional group; this built-in handle enables the compound to take part directly in copolymerizations and grafting reactions. By building the ionic liquid directly into a polymer matrix, you sidestep many of the leaching and migration problems that occur with more traditional non-functionalized imidazolium salts.
Not every ionic liquid can operate in electrochemical devices. We’ve run direct comparative trials, putting [C8VIm][BF4] against similar alkyl imidazolium tetrafluoroborates. The presence of the octyl chain reduces viscosity compared to longer alkyl analogues, making this variant easy to handle, dispense, and mix. It offers a balanced hydrophobicity, which allows pairing with non-aqueous reaction systems. This provides an advantage in dye-sensitized solar cells and other devices where traditional hydrophilic ionic liquids risk phase separation or performance losses.
Some buyers look only at the cation and miss the impact of the anion on chemical compatibility, so here’s an inside perspective. The tetrafluoroborate anion (BF4) confers significant electrochemical stability and keeps ionic conductivity high, especially under elevated voltages or mild heating. Where many industrial grades of imidazolium salts fail by forming sludge or losing conductivity, we see [C8VIm][BF4] staying clear and high-performing. Only real head-to-head runs in demanding settings separate these subtle performance traits, and we’ve run those tests: moisture sensitivity, volatility under vacuum, and resistance to hydrolysis all show marked improvement over PF6 and Cl- analogs.
A key operational difference comes with the functional vinyl group on the imidazolium ring. A standard octylimidazolium salt offers inert solubility, but the vinyl group changes the game by giving a direct role in chemical modification, especially in the creation of polymerizable networks and grafted materials. Chemists can utilize this reactivity for the in-situ formation of ion-conductive membranes or new classes of ion gels. With the octyl chain, the compound bridges the gap between purely hydrophilic ionic liquids and those prone to form distinct phases or precipitates.
Our production site engineers have fielded dozens of calls from process technicians looking to troubleshoot complex syntheses plagued by heat build-up or poor separation of phases. We purposefully developed [C8VIm][BF4] to handle real-world process challenges. In biphasic catalysis, the extra octyl group adds sufficient hydrophobicity, which ensures resolvable product slugs and maintains stable phase boundaries even in the presence of non-polar substrates. During scale-up, we’ve observed that batch reactors don’t foul as quickly, and post-reaction workup requires less wash solvent compared to similar ionic liquids that lack the vinyl group.
The practical impact here can't be overstated: in pilot plant tests, operators note the ease of product handling and waste minimization. Ionic liquid recovery and recycling see a boost due to lower water solubility, which is critical for companies looking to close solvent loops or reduce environmental impact. For users needing to extract metals or organics, the adjustable polarity means [C8VIm][BF4] can selectively partition a range of polar and non-polar compounds without swelling or decomposition under moderate thermal loads. It’s the difference between a reagent that lives in the back of the supply closet and one that becomes a staple in day-to-day process chemistry.
The value of a robust ionic liquid like [C8VIm][BF4] stands out most in labs focused on innovative separation processes and electrochemical energy devices. Many universities and battery start-ups have shared their project data with us, showing measurable benefits in coulombic efficiency and cycle stability when using our product over generic, lower-purity imidazolium salts. For solid-state battery research, [C8VIm][BF4] forms a stable electrolyte system resistant to both hydrolysis and solvent evaporation, supporting continuous cycling without catastrophic voltage drop or material bleed-out.
In extraction chemistry, teams using supercritical CO2 or non-polar organic solvents have found this ionic liquid allows more tunable partitioning, giving greater control and higher yields in metal and organic product recovery. The vinyl handle delivers options for further derivatization—researchers looking to affinity-tag, crosslink, or immobilize reagents gain an extra layer of versatility without laborious multi-step syntheses. This type of flexibility speaks to real user needs, not just what fits inside a catalog entry or spec sheet. Our technical support staff routinely works with industrial partners, adjusting production conditions to accommodate customer-specific clean-up protocols or scale constraints.
Chemical sustainability doesn’t happen by accident; it comes from precise formulation, rigorous process control, and dedication to purification steps that less disciplined operations overlook. We set our benchmarks high—purity thresholds get monitored from raw material intake through fractional distillation and anion metathesis to bottled product. Each batch undergoes in-house GC/MS and NMR screening, plus ion chromatography for residual halides. The environmental advantage of [C8VIm][BF4] comes from its low volatility and limited aquatic toxicity; with controlled disposal and recycling protocols, users can dramatically reduce solvent emissions compared to volatile alternatives such as acetonitrile or dichloromethane.
The lower vapor pressure eliminates many fugitive emission concerns. In actual plant settings, operators run less risk of hazardous vapor inhalation, and there is minimal atmospheric loss during open transfers or minor spills. We see downstream partners in pharmaceutical, photonics, and electronics sectors choosing our product for this reason. Repeated cycles reveal negligible decomposition even after prolonged exposure to electrolytic potentials or elevated reaction temperatures (often up to 120°C), cutting down on material waste and replacement frequency.
Over the past two years, our in-house development chemists have supported dozens of customer applications ranging from template-directed synthesis of porous polymers to high-stability capacitive media and next-generation responsive coatings. One long-term client uses [C8VIm][BF4] to produce ion-conductive networks for organic solar films, achieving film uniformity and conductivity metrics that outperform polyethyleneglycol-based systems by close to 30%. Our review of their production records finds defect rates held below 2%, with no gel phase separation across more than 20 batches.
Another industrial partner supplies micro-batteries to IoT device manufacturers. Their technical teams observed that incorporating [C8VIm][BF4] at the interface layer extends operational stability and capacitance retention, citing routine 95% efficiency retention after 5,000 charge/discharge cycles. By embedding the vinylimidazolium group into polymer electrolytes, their end-products maintain ionic conductivity even in miniaturized cells exposed to high-frequency cycling. Synthetic chemists in pharmaceutical labs could also corroborate improved yields and better selectivity in transition-metal-catalyzed processes run in an [C8VIm][BF4] phase; recycled product streams showed no accumulation of organic side products, a constant risk with more conventional, less pure imidazolium salts.
The most revealing feedback has come from academics running cross-disciplinary catalysis projects. Where traditional ionic liquids sometimes stunt catalyst turnover number (TON) due to side reactions, the functional vinylimidazolium salt offers inertness until triggered, reducing background reactivity and extending catalyst lifetime. Their published work documents two- to three-fold improvements in product formation rates. Such results underscore the distinction between a fully characterized, precisely manufactured batch and a generic, off-color, poorly defined product from less-experienced manufacturers.
Routine experience in chemistry production means knowing real supply challenges, stability concerns, and obstacles of shifting from milligram research quantities to tens-of-kilograms, or even ton-scale operations. Every plant manager fights moisture contamination, batch color drift, or inconsistent viscosity—a variance traceable in poorly purified ionic liquids. We’ve fine-tuned our production train for minimal water pickup at every handling step, incorporating vacuum drying and inert gas purges through transfer lines and filling heads. Each filled container leaves with a controlled headspace and seals tested for environmental ingress.
Customers asked us to quantify shelf life, not just offer reassurances. We’ve trended retain samples over twenty-four months at standard warehouse temperatures and found no substantial loss of performance in electrochemical, catalysis, or polymer incorporation applications. Such resilience comes down to rigorous precursor screening—octyl bromide, imidazole, and vinyl bromide—alongside sequential purification and fractionated addition of the tetrafluoroborate anion. Operators record every critical process variable; traceability back to feedstock lot allows us to rapidly zero in on possible sources of variance long before issues reach the customer site.
By working closely with formulation scientists, process engineers, and bench-top researchers, we’ve built up a concrete understanding of what successful applications demand. They need ionic liquids that neither degrade under thermal cycling nor introduce contaminants conflicting with end-use requirements. For users stepping up to full-scale manufacturing, unnecessary byproducts or unstable halide residues translate directly to lost yield and equipment fouling. Our in-house QC team regularly reviews inbound and outbound data with direct user feedback, making continuous improvement a company-wide standard practice.
For those working on custom polymer synthesis, the reliability of the vinyl-functionalized imidazolium ring means fewer failed reactions and higher repeatability. Process engineers, burdened with strict safety targets and solvent recovery thresholds, have told us that the hydrophobic balance of the octyl chain mitigates stratification or phase-separation headaches often seen with shorter or longer alkyl cations. We routinely see less downtime and greater ROI for those clients that work with our consistent, fully characterized material.
The field of ionic liquids keeps diversifying—energy storage, synthesis, device fabrication, extraction, and analytical chemistry all benefit from the kind of stability, versatility, and workflow compatibility that [C8VIm][BF4] brings. By integrating feedback loops between R&D, manufacturing, and direct end users, we continually refine not just batch quality but broader process recommendations and troubleshooting guides. Direct partnerships with large-scale users drive us to keep improving. Each unique application gives us more raw data and case examples for improving purity, reducing environmental impact, and locking in reproducible function. Our R&D team remains focused on new variants with further functionalization of the imidazolium ring, or the careful adjustment of the alkyl chain to open up even more specialized application niches.
From first-run academic synthesis to validated multi-ton campaigns for battery and pharmaceutical manufacturers, our standard for quality and process transparency ensures that every order meets the strictest research and commercial criteria. Years of hands-on experience, robust quality tracking, and focused user support distinguish every batch of [C8VIm][BF4] produced on our line.
The role of [C8VIm][BF4] has shifted in practice from an academic or curiosity-based additive to an essential building block for transformative industrial and research processes. The direct input from chemists, engineers, and technicians shapes how we formulate, purify, and guarantee our product. For those seeking more than just a catalog reference or data sheet, proven, well-characterized materials with an open feedback channel remain the smart choice. Years of accumulated practical experience guide every kg we prepare, from the first reaction flask to bulk delivery tanks. [C8VIm][BF4] stands out not by flashy branding, but by consistent, tested, documented results in advanced chemistry.