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HS Code |
413059 |
| Chemical Name | 1-Octyl-2,3-Dimethylimidazolium Tetrafluoroborate |
| Cas Number | 933750-43-7 |
| Molecular Formula | C13H25BF4N2 |
| Molecular Weight | 312.16 g/mol |
| Appearance | Colorless to pale yellow liquid |
| Purity | Typically ≥98% |
| Melting Point | -17 °C |
| Boiling Point | Decomposes before boiling |
| Solubility In Water | Miscible |
| Density | 1.08 g/cm³ (at 25 °C) |
| Refractive Index | 1.457 (at 20 °C) |
| Storage Conditions | Store at room temperature, tightly closed |
| Smiles | CCCCCCCCn1c(C)n(c2nccn2)c1.[BF4] |
| Ec Number | none assigned |
| Hazard Statements | May cause skin and eye irritation |
As an accredited 1-Octyl-2,3-Dimethylimidazolium Tetrafluoroborate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | A 100g amber glass bottle with a tight-sealing cap, labeled “1-Octyl-2,3-Dimethylimidazolium Tetrafluoroborate,” hazard warnings displayed. |
| Shipping | 1-Octyl-2,3-Dimethylimidazolium Tetrafluoroborate is typically shipped in sealed, chemical-resistant containers to prevent moisture absorption and contamination. It should be handled as a potentially hazardous chemical, following all applicable regulatory guidelines for transport, including labelling and documentation. Shipping is conducted under ambient conditions, unless otherwise specified by the supplier or MSDS. |
| Storage | 1-Octyl-2,3-Dimethylimidazolium Tetrafluoroborate should be stored in a tightly sealed container in a cool, dry, and well-ventilated area. Protect it from moisture and direct sunlight. Keep away from strong oxidizing agents, acids, and bases. Recommended storage temperature is room temperature (15–25°C). Ensure proper labeling, and avoid storing near incompatible substances to maintain chemical stability and safety. |
Applications of 1-Octyl-2,3-Dimethylimidazolium Tetrafluoroborate in Industrial ManufacturingAs a direct chemical producer, we ensure that each manufacturing sector using 1-octyl-2,3-dimethylimidazolium tetrafluoroborate receives full technical data and integration support. Below we detail the key industrial applications, focusing on specification, regulatory alignment, production dosage, implementation stage, and targeted end-products. 1. Electrolytes for High-Performance Supercapacitors1-Octyl-2,3-dimethylimidazolium tetrafluoroborate sees strong industrial use as an ionic liquid electrolyte in high-voltage supercapacitor cells. Its high ionic conductivity and electrochemical stability support energy density increase and cycle life extension, especially in cells using activated carbon or graphene-based electrodes. Leading capacitor manufacturers require rigorous impurity control and performance validation before deploying this raw material in production-scale cells, with precise adjustment of ionic liquid content during electrolyte formulation to balance viscosity and conductivity. Industry compliance standards
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2. Catalytic Media in Organic Synthesis for Pharmaceutical IntermediatesThe compound functions as a nonvolatile ionic liquid medium and phase-transfer catalyst during the regioselective alkylation and nucleophilic substitution of key pharmaceutical intermediates. The purity and controlled water content allow synthetic chemists at GMP facilities to perform multi-step reactions under mild conditions, minimizing the formation of byproducts and supporting easier downstream extraction. Validation involves both on-line HPLC purity checks and direct comparison to non-ionic liquid process alternatives, to document reduced solvent waste and improved catalyst lifetime. Industry compliance standards
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3. Lubricant Additive in Precision Industrial Gear SystemsThis ionic liquid integrates into advanced synthetic lubricants for high-load, high-temperature gear assemblies in both robotics and process automation. When blended at controlled dosages, it enhances tribological properties, reduces friction, and extends service intervals by enabling stable boundary lubrication. Leading lubricant compounders implement specification control for water content and ionic contaminant levels to ensure no negative interaction with seals or polymer-coated bearings during in-service operation. Industry compliance standards
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4. Extraction Agent in Hydrometallurgical Metal RefiningRefiners utilize this ionic liquid as a selective extractant for rare earth and precious metals in solvent extraction columns. Industrial users verify phase separation efficiency, reusability over multiple cycles, and compliance with environmental discharge thresholds. During extraction, the material captures metal ions selectively from acidic aqueous phases, facilitating recovery, especially for elements such as gold, palladium, and lanthanides. The process also benefits from the thermal stability and low vapor pressure, which minimise loss during multi-stage countercurrent operation. Industry compliance standards
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Competitive 1-Octyl-2,3-Dimethylimidazolium Tetrafluoroborate prices that fit your budget—flexible terms and customized quotes for every order.
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Making ionic liquids over the years, we have seen the demand shift from simple imidazolium salts to more tailored options with longer chains and functional side groups. Our production line for 1-Octyl-2,3-Dimethylimidazolium Tetrafluoroborate grew out of direct requests from research chemists, process engineers, and advanced battery developers. Buyers wanted an ionic liquid that balances hydrophobicity, chemical stability, and operational flexibility, so we designed our workflow to supply this grade dependably and at scale. The model we manufacture today, often coded as OMIM BF4, offers the 1-octyl backbone for greater hydrophobic character compared to shorter alkyl substitutes. The two methyl groups next to the nitrogen ring make the cation bulkier, tightening its liquid range and dialing back melting tendencies common in more symmetric analogs.
Our process, refined after countless batches, starts with high-purity imidazole raw material. The alkylation steps require continuous monitoring. Shortcuts might produce higher yields per vessel run, but we emphasize consistency and strict impurity profiles. Trace water, improper reagents, or incomplete side reactions quickly produce product outside customer requirements, especially for those involved in electrochemical studies or synthesis catalysis. Most of our regularly shipped batches measure well below the 200 ppm water mark, and our anion exchange installs the tetrafluoroborate with process controls focused on minimizing hydrolysis and related byproducts.
We deliver 1-Octyl-2,3-Dimethylimidazolium Tetrafluoroborate mainly as a clear, low-viscosity liquid. Most lots exhibit purity upwards of 99%, confirmed by NMR and ion chromatography for cation and anion identification, alongside Karl Fischer for moisture. Density averages near 1.1 g/cm3 between 20–25°C, a touch less dense than shorter-chain analogs, reflecting the influence of the octyl group. Thermal stability extends past 300°C, proven by repeated TGA testing on our in-house equipment.
Typical packaging for this compound is glass or fluoropolymer bottles. We avoid HDPE for bulk since the liquid can leach plasticizers or compromise packaging over the course of longer storage or shipment. Scale-up production takes place in glass-lined steel reactors, with GC and ICP-OES checks at each inlet and harvest checkpoint. By integrating continuous online drying systems and closed-system transfer, we cut down on both water pickup and operator exposure.
In lab-scale synthesis, customers gravitate toward OMIM BF4 for its resilience across a range of solvents and elevated temperatures. Chemists using palladium or copper catalysis found the higher viscosity compared to shorter alkyl imidazoliums required minor stirring adjustments but improved recovery and reuse cycles. The ion pair’s thermal window means it doesn’t degrade or discolor during long reflux steps. Several academic partners used it as a solvent or co-solvent in cross-coupling reactions, and their published reports highlighted fewer side products relative to more common ionic liquids.
Our industrial accounts focus on battery and electrode formulations. Large-scale lithium-ion battery labs regularly source OMIM BF4 for electrolyte additives. The low volatility, low flammability, and high electrochemical stability give it advantages in next-generation cell chemistries. Internal evaluations show ion conductivity levels roughly 0.6 mS/cm at room temperature, outperforming shorter alkyl analogs in layered oxide or silicon anode blends. Reliability is a recurring theme—engineers value the consistent dielectric constant and broad thermal window that supports testing from ambient through moderate elevated temperatures without performance drift or thermal runaway.
In separation applications, we work closely with teams extracting rare earths and transition metals. OMIM BF4 exhibits efficient phase transfer and selectivity. Unlike shorter alkyl imidazolium variants, the octyl chain here improves extraction efficiency for heavy metals by favoring less polar complexes. Our on-site team completed a project purifying nickel from ore leachates; the ionic liquid retained separation power even after repeated extraction/stripping cycles, matching performance without significant impurities or viscosity buildup.
Our daily interactions with academic and industrial development chemists highlight the growing awareness of nuanced property differences among ionic liquids. Shorter chain versions—methyl or ethyl—pour easily, cost a little less, and display lower viscosities, supporting higher ion mobility for electrochemical sensors or rapid-mixing reactions. Yet they draw more water from air, show higher volatility, and sometimes degrade in extended-use scenarios. Longer alkyl variants, like decyl or dodecyl, weigh down viscosity further and pose more handling challenges without delivering proportionate gains in application performance, except in specialized extraction or lubrication tasks.
With two methyl groups on the imidazolium ring, OMIM BF4 creates a more asymmetric charge environment than the popular 1-butyl-3-methylimidazolium salts. This matters for researchers tuning liquid crystal domains, custom electrolyte formulations, or reaction medium selectivity. The methylated sites at positions 2 and 3 block hydrogen bonding and potential C2-H reactivity, enhancing stability under both acidic and basic catalysis. We have tracked lower breakdown rates in long-duration tests, with repeated potential cycling in battery prototypes and resistance to byproduct formation even in sulfur-rich reaction environments.
Our customers weighing OMIM BF4 against 1-butyl-3-methylimidazolium tetrafluoroborate share that the additional octyl group delivers superior hydrophobicity and aggregate control in mixed organic/aqueous systems. This comes into play during phase separation, especially when targeting lipophilic or amphiphilic analytes. One pharmaceutical client wrote in about improved yields during column chromatography extractions, echoing many other customers moving away from shorter-chain ionic liquids for better reproducibility in their protocols.
Every manufacturer aims for tight quality control, but our scale and process investments push us beyond simple batch sampling. Automated systems sample each reactor run for water content, impurity ions, and organic contaminants. Often, returning clients ask about the trace heavy metal content; our products meet the <1 ppm specification for most metals. If we suspect any deviation, even at the parts per billion level, we rerun the purification sequence using high-performance flash columns. The tetrafluoroborate anion’s stability, compared to PF6 or NTf2, simplifies product handling as it does not generate corrosive fluorides under storage or on mild heating.
Customers occasionally request batch records or regulatory documentation for registration or compliance filings. We keep a digital paper trail—from reagent lot codes to final packaging dates—stretching back over a decade. Laboratories requiring repeat orders or validation can reference this for reproducibility studies and long-term research programs.
We repackage all OMIM BF4 in a humidity-controlled cleanroom suite. Each bottle is filled, capped, and sealed while exposure to ambient air sits below 2 minutes. Tying packaging—and not just production—into our quality loop reduces lot variability and keeps active chemical properties at specification for months in storage, assuming containers remain sealed and protected from direct sunlight.
Behind the finished product, our crew faces daily decisions between yield maximization and purity assurance. Shortcutting drying steps or overlooking a small contaminant spike means facing dozens of reformulations downstream. We have replaced several types of dryer columns and filtration cartridges to keep ionic liquids moisture free. Plant operators monitor every reactor with IR and NMR probes, looking for byproducts or foam buildup that signal incomplete reactions.
Scaling up from 500-gram glassware batches to 200-liter tanks brought home the importance of precise temperature control. The long octyl chain can crystallize or oil out before complete methlyation occurs, so intermediate transfers are heated and mixed intensively. We designed the plant flow for minimal atmospheric transfer, investing in jacketed lines and nitrogen-blanketed storage tanks to keep every intermediate batch fresh and consistent.
Shipping presents its own challenges. Couriers might shake, tilt, or even expose packages to extreme cold. Over the years, we tested a dozen seal types before settling on fluoropolymer liners that hold up better than metal or regular glass. Customers in hot climates trust that our containers won’t break down or leak ionic liquid during storage, maintaining the physical and chemical integrity all the way to their lab or production floor.
Chemical manufacturers live by their products’ reputations. The true benchmarks come not from marketing blurbs but from repeated feedback on real-world usage—where our OMIM BF4 gained a firm foothold. Organic chemists often report improved selectivity during multi-step synthesis, with less cation exchange interference and increased catalyst turnover numbers. Extractive metallurgists value the stability of the ionic pair under oxidizing conditions, making transition from laboratory scale to field pilot plants far smoother. In electrochemistry circles, battery and capacitor developers reiterate that conductivity and voltage stability match published literature and hold steady over many charge cycles. They highlight the minimized side-reactions, noting a drop-off in cell gassing events and resistivity spikes common to more reactive, shorter chain ionic liquids.
Pharmaceutical and flavor/fragrance chemists exploit OMIM BF4 for partitioning and purification. Several partners shared with us their success scaling bench-top purification methods to preparative chromatography, routinely hitting higher yields and fewer interferences than with competitor-grade materials. With most applications, improved recyclability becomes evident: customers can wash and recover the liquid multiple times without sacrificing purity or performance, extending value further and supporting sustainability goals.
Environmental research teams appreciate how OMIM BF4 provides a less volatile, easier-to-contain alternative to organic solvents. Academic groups published studies quantifying lower air and soil emissions compared to older solvent systems, opening up research in greener chemistry. Many industrial partners look to us as a supplier who validates claims with batch records.
Producing, packaging, and delivering OMIM BF4 in a competitive global market comes with its share of obstacles. Sourcing ultra-high-purity imidazoles and borates depends on consistent upstream chemical supply. Disruptions anywhere along the chain—such as refinery interruptions, transport delays, or impurity surges in core reagents—cascade directly to production schedules and customer lead times. We invest heavily in supplier relationships, long-term contracts, and on-site quality checks to keep these issues to a minimum.
Global transport rules list tetrafluoroborate salts as less restrictive compared to many other ionic liquids, reducing paperwork and customs holdups. For customers seeking additional safety or environmental assurances, we help support application-specific requests by providing detailed breakdowns of stability, decomposition pathways, and emissions.
Ongoing customer feedback drives product evolution. Early adopters pushed us to enhance both packaging and analytical support, building in low-detectable-impurity reporting and supporting faster order cycles. We routinely survey end-users for improvement ideas, leading to tweaks in drying cycles or line purging to cut trace contamination. Customers with specific application requirements—such as ultra-low heavy metals for battery work or ultra-low halides for synthesis—can request customized lots, which our team manages throughout the manufacturing process with full documentation.
Years of direct experience refining OMIM BF4 production lets us answer not just “what,” but also “why.” Customers get more than a material—they gain a partner with day-to-day insight and practical knowledge. Fielding calls about unexpected solvent compatibility, long-term sample shelf life, or scale-up strategies comes with the territory, and we treat these conversations as essential to continuous improvement. No speculation, just real-world troubleshooting based on decades of hands-on chemical experience.
From outset planning to batch production and final packaging, we stay keenly aware that end users depend on every variable of our process for their product’s success. That’s real-world manufacturing: honest reporting, strict controls, and open exchange. We measure our success by your results and stand ready to address the next round of technical challenges in close partnership with every customer.