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HS Code |
626619 |
| Chemical Name | 1-Hexyl-3-Methylimidazolium Hexafluoroantimonate |
| Chemical Formula | C10H19N2SbF6 |
| Molecular Weight | 412.13 g/mol |
| Appearance | Colorless to pale yellow liquid |
| Melting Point | Approx. -46 °C |
| Boiling Point | Decomposes before boiling |
| Density | 1.24 g/cm³ (at 20°C) |
| Solubility In Water | Miscible |
| Cas Number | 149461-28-1 |
| Refractive Index | 1.442 (approx.) |
| Storage Temperature | Store at room temperature |
| Purity | Typically >98% |
| Odor | Odorless |
| Stability | Stable under recommended conditions |
As an accredited 1-Hexyl-3-Methylimidazolium Hexafluoroantimonate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Brown glass bottle, 100g net weight, tightly sealed with screw cap; labeled with chemical name, hazard symbols, and manufacturer details. |
| Shipping | 1-Hexyl-3-methylimidazolium hexafluoroantimonate should be shipped in tightly sealed containers, away from moisture and incompatible substances. It must be packed according to chemical safety regulations, labeled correctly, and transported under appropriate temperature and hazard controls. Handle as a potentially toxic and corrosive material, following all relevant shipping guidelines for hazardous chemicals. |
| Storage | 1-Hexyl-3-methylimidazolium hexafluoroantimonate should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from moisture, heat, and incompatible substances such as strong acids or bases. Protect from direct sunlight and sources of ignition. Use secondary containment to prevent environmental release, and clearly label storage containers to ensure safe handling and identification. |
Applications of 1-Hexyl-3-Methylimidazolium Hexafluoroantimonate in Industrial ManufacturingAs a direct manufacturer of 1-Hexyl-3-Methylimidazolium Hexafluoroantimonate, we support global industrial partners in supplying this advanced ionic liquid across selected process-critical downstream sectors. The following sections detail established application scenarios, including formulation details, compliance references, and integration into specialized manufacturing workflows. All data reflects actual customer adoption and ongoing regulatory requirements. 1. Lithium-Ion Battery Electrolyte AdditivesManufacturers of high-energy-density lithium-ion batteries employ this ionic liquid to enhance ionic conductivity, improve thermal safety, and suppress dendrite formation. Its high electrochemical stability allows for thinner electrodes and greater cell longevity, particularly in advanced automotive and energy storage applications. Industry compliance standards
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2. Catalytic Medium in Fluorination ChemistryIn halogen-based synthesis for agrochemical and pharmaceutical intermediates, this ionic liquid functions as a homogeneous catalyst and medium for selective fluorination reactions. Its high fluorine compatibility, combined with low volatility and minimized side-product formation, supports the scaling of continuous-flow reactions involving antimony catalysts. Industry compliance standards
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3. Antistatic Coating Formulations for Microelectronics PackagingPrecision packaging operations for semiconductors and PCBs require permanent antistatic protection to prevent ESD damage. This ionic liquid is incorporated into the topcoat layer, where its persistent ionic character imparts surface conductivity and resists migration even under thermal cycling. Industry compliance standards
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4. Solvent for Gas Separation Membrane ProductionEngineered membrane manufacturers utilize this ionic liquid in polymer casting solutions for the fabrication of selective gas separation membranes. Its tailored solvation properties enable precise phase inversion and pore structure, particularly for CO2/N2 and SO2 filtration in industrial emissions control. Industry compliance standards
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5. Electroplating Bath Additive for Precious Metal RecoveryIn metal finishing and precious metal recycling, this ionic liquid serves as an additive in antimony and gold electroplating baths. Its ability to modulate ion transport and deposit morphology leads to finer grain and higher purity coatings on electronic components, while minimizing unwanted side-reactions. Industry compliance standards
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Producing reliable imidazolium salts in a busy chemical plant takes more than a batch reactor and a few clean flasks. For over a decade, we’ve worked on imidazolium ionic liquids, paying close attention to every step—solvent drying, anion exchange, purification, even how we handle the ambient humidity at the transfer point. Some materials test the patience of chemists. 1-Hexyl-3-methylimidazolium hexafluoroantimonate stands among them. With its unique ion pairing and long hexyl chain, it offers a combination rarely encountered: chemical endurance, readiness to dissolve tough solutes, and a physicochemical profile that serves complex reaction systems.
Unlike lighter cations or simpler anions, this hexyl-methylimidazolium variant doesn’t splash into organometallic catalysis or advanced separations as a generic salt. From the first batch, we noticed its viscosity, hydrophobicity, and thermal window stand apart from shorter-chain options or salts like PF6- and BF4-. The hexafluoroantimonate anion brings a stability edge, meaning researchers get longer bench-life and less risk of degradation or hydrolysis in tricky air- or moisture-sensitive setups.
We’ve run thousands of kilograms through our systems and spent long hours checking every lot. Typical product delivers as a colorless to pale yellow liquid at room temperature; even minor impurities can cause tinting, which we catch with strict UV-Vis and NMR routines. Hexyl substitution boosts the melting point over ethyl or butyl homologues, yet still supports liquid handling in ambient lab conditions for most months. Lab teams value the high density and low vapor pressure, which helps with storage, transfer, and process charging in scale-up work.
Handling the hexafluoroantimonate anion brings its own lessons. Not all production lines manage halide removal with equal finesse, but our protocols reduce trace halide well below visible precipitation limits in applications like lithium salt separation or phase transfer catalysis. Our analytical chemists worked hard to confirm the absence of chloride or bromide, using both routine ionic chromatography and independent elemental analyses after each production cycle.
We’ve learned that customers demand secondary confirmation of identity and quality, not just a lot sheet. We regularly share full spectral sets, including 1H, 13C, and 19F NMR, plus mass spectrometry on request. The model we supply to academic and industrial research groups is typically labeled as [HMIM][SbF6], reflecting both the structural assignment and anion pairing. Most of our partners order at purity levels above 99%, but we maintain rigorous water content controls, using Karl Fischer titration to ensure the moisture stays under 0.05%—essential for air- and water-sensitive syntheses.
Viscosity, conductivity, and density reports frequently go out with shipments, since even small batch-to-batch variations can affect ion mobility in electrochemical research or liquid–liquid extraction. As manufacturers, we prioritize consistency by running parallel instrumentation in every batch record. If you’re developing any process where ion transport or solubility strongly influences outcome—like tunable solvents, electrodeposition, or multi-phase catalysis—these metrics carry more weight than the theoretical data sheets you see online.
There are plenty of imidazolium ionic liquids, so why do R&D teams keep returning to this one? The longer hexyl chain improves partitioning in nonpolar and mixed-phase systems, making it appealing for catalysis protocols where selectivity and product separation are tough using shorter-chain analogues. When compared to imidazolium salts carrying PF6- or BF4-, we see measurable improvements in chemical stability, especially at elevated temperatures. SbF6- brings less hydrolytic fragility than PF6-, so shelf-life for both the neat liquid and dissolved stocks stretches longer under standard storage.
Chemists running transition metal catalyzed reactions often complain about background reactivity with coordinating anions. Our customers have described smoother, more reproducible results when using 1-hexyl-3-methylimidazolium hexafluoroantimonate in palladium and ruthenium-catalyzed transformations, particularly isomerizations and oxidative additions. In contrast, halide or triflate anions sometimes encourage unwanted ligand redistribution, which this material avoids. This performance gain reflects years of incremental improvements: we don’t just follow literature recipes but update our plant based on chemists’ direct operational feedback.
There’s often an assumption that all ionic liquids are interchangeable, but that falls apart in real-world operations. In electrochemistry, for example, the high purity and low halide content translate to far lower background currents, making this material particularly valuable for studies on electrode interfaces or for as base electrolytes in battery research. As a solvent or phase transfer agent, it handles alkylation and nucleophilic substitution processes where solvents like acetonitrile or DMF fail to deliver adequate selectivity or stability.
On the larger scale, our material supports pilot plant and kilo-lab teams focused on renewable materials and next-generation recycling. One partner in polymers takes advantage of its hydrophobicity to solubilize challenging initiators for ring-opening polymerizations while reducing hazard risks compared to legacy aromatic solvents. Another product development group benefits from its non-coordinating nature for catalyst separation in continuous flow hydrogenations.
Anyone who has scaled ionic liquids knows that synthesis purity, washing, filtration, and even ambient handling shape performance at the customer site. We’ve learned that it doesn’t take much—less than a tenth of a percent of extraneous halide or residual solvents—to derail a sensitive reaction or phase study. By keeping batch records tied to wet chemistry, gravimetric analysis, and customer feedback, we reduce both process downtime and call-backs. In recent years, we expanded our quality control team to include process analysts who’ve spent time on high-throughput screening lines, not just analytical benches.
Shipping ionic liquids across continents isn’t easy either. Some products pack fine in standard polymer drums, but 1-hexyl-3-methylimidazolium hexafluoroantimonate performs best stored in amber glassware with robust physical seals, which our logistics account for. Careful packaging keeps out dust and air—details that matter when partners operate under GMP or ISO 9001 oversight.
A few years back, we partnered with a university electrochemistry group testing ionic liquid conductivity at subzero temperatures. They found our [HMIM][SbF6] maintained higher ionic mobility and less viscosity swing during freeze-thaw cycles compared to comparable PF6- or BF4- salts. Their data matched what our pilot plant engineers had witnessed—the unique hexafluoroantimonate structure resists salt-out even after multiple cool-downs, which makes it more rugged for repeated temperature cycling.
Some complex catalysts exhibit exceptional activity in [HMIM][SbF6], yet show poor turnover in Br- or Cl- salts. We see this difference whenever we serve research groups advancing next-generation pharmaceuticals or polymers that demand high-purity, low-nucleophilicity solvents. In these applications, the low nucleophilicity and strong oxidative resistance mean improved yield, easier separation, and longer catalyst lifespans. We’ve traced unexpected fouling in lesser-prepared ionic liquid competitors to residual halide. Our own labs corrected for this over a decade ago by introducing trace-level validation protocols, which further separates our batches from third-party resellers who lack source control or process transparency.
Not long ago, sustainability was an afterthought for specialty ionic liquid production. Times have changed. Our plant has shifted toward closed solvent loops and uses advanced scrubbers to minimize emissions of fluorinated byproducts, both to protect our team and reduce our environmental impact. Academic users often ask whether our supply is sourced sustainably—our modern plant keeps solvent waste below regulatory thresholds, and our process waters get recycled.
Green chemistry research needs consistent solvent properties and ultra-low impurity loads. 1-hexyl-3-methylimidazolium hexafluoroantimonate enables catalyst recycling, allows selective extractions, and cuts out the need for hazardous VOC solvents. We’re committed to keeping the quality uncompromised even as markets demand ever-stricter environmental compliance. Maintaining transparency—by publishing environmental data and working with downstream companies seeking lifecycle assessments—remains core to our operation.
Questions about scale-up or custom synthesis routes aren’t left to junior sales teams at our manufacturing site. Chemists who've worked with this compound directly handle technical queries and are available to suggest application strategies grounded in production-scale realities, not just catalog descriptions. Some users ask about surface tension modification, others about extraction efficiency with rare earth metals, or temperature-dependent physical data relevant to their reactors. We’re open about what our real-world data supports, sharing process notes where possible to improve transparency.
More often than not, success boils down to details: water content measured just before dispatch, halide screening on representative samples, headspace GC checks to verify no volatile contaminants. This has helped dozens of material science groups avoid setbacks caused by subtle quality issues. These aren’t features easily guaranteed by intermediaries who never see a reactor or titration flask.
Not every project runs smoothly in practice. Many R&D labs hit roadblocks with solvation issues, overlapping impurity peaks in NMR, or inconsistent phase formation during liquid–liquid extractions. We learned early not to dismiss these as user error. Instead, we maintain a set of recommended protocols for sample drying, filtration, and solvent blending, based on batches that performed best in published studies and direct industrial trials.
Some partners encountered inconsistencies when scaling from milligram to kilogram synthesis and traced them to minor atmospheric water absorption. In response, we invested in closed-hood packaging and rapid-transfer airlocks for larger volumes. For customers tackling hydrophobicity or partition coefficient challenges, we provide empirical data instead of theoretical predictions—this builds trust and reduces costly process experimentation.
The market for specialty ionic liquids keeps growing, but many suppliers rely on redistribution of outside brands, risking label swaps or impurity creep between shipments. Our operation keeps every batch under our manufacturing team’s direct control, with traceable certificate of analysis and ongoing batch-specific QA. Our partners—from national labs to fine chemical producers—often come to us after a single failed run using reseller lots. It’s not just about purity numbers on a sheet; it’s the lived experience handling unforeseen problems and building fixes into every stage of the manufacturing process.
Feedback from hundreds of researchers helped us design our protocol for 1-hexyl-3-methylimidazolium hexafluoroantimonate. Instead of focusing on a narrow spec set, we optimized for what end-users actually observe: clean dissolution in nonaqueous systems, predictable behavior with transition metals, low thermal decomposition rate under continuous heating, controlled moisture ingress, and packaging that supports long-term storage. Aligning our output with real-life synthetic demands took countless iterations, but it’s what keeps customers returning batch after batch.
Our approach to manufacturing 1-hexyl-3-methylimidazolium hexafluoroantimonate has grown out of daily interaction with both chemistry and engineering teams who understand the demands of industrial and research-scale projects. Every improvement—from purification technique adjustments to batch record transparency and product support—originated in feedback from tough runs and laboratory troubleshooting. This hands-on history informs our technical recommendations and enables better chemistry in your lab or plant setting.
Partnering with a direct manufacturer means gaining more than product access; it means a working relationship with a team steeped in the chemistry of imidazolium salts and ready to evolve with your technical needs. Whether you’re looking to solve a solubility bottleneck or expand catalysis in green solvent regimes, the reliability of 1-hexyl-3-methylimidazolium hexafluoroantimonate, produced with care and accountability, builds both trust and technical progress in demanding chemical environments.