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HS Code |
927707 |
| Chemical Name | 1-Hexyl-2,3-Dimethylimidazolium Bis((Trifluoromethyl)Sulfonyl)Imide |
| Abbreviation | C6C1C1Im NTf2 |
| Cas Number | 632614-45-0 |
| Molecular Formula | C15H25F6N3O4S2 |
| Molecular Weight | 527.5 g/mol |
| Appearance | Colorless to pale yellow liquid |
| Density | 1.35 g/cm3 (approximate) |
| Melting Point | -30 °C (approximate) |
| Boiling Point | Decomposes before boiling |
| Solubility | Miscible with water and many organic solvents |
| Ionic Liquid | Yes |
| Purity | Typically ≥ 98% |
| Conductivity | High ionic conductivity |
| Thermal Stability | Up to ~350 °C |
| Common Uses | Electrolytes, solvents, catalysis |
As an accredited 1-Hexyl-2,3-Dimethylimidazolium Bis((Trifluoromethyl)Sulfonyl)Imide factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle, 100g content, tightly sealed with PTFE-lined cap, chemical-resistant label stating “1-Hexyl-2,3-Dimethylimidazolium Bis((Trifluoromethyl)Sulfonyl)Imide, 100g, for laboratory use only.” |
| Shipping | This chemical, **1-Hexyl-2,3-dimethylimidazolium bis((trifluoromethyl)sulfonyl)imide**, is shipped in sealed, chemical-resistant containers compliant with international hazardous materials regulations. It is labeled per GHS guidelines and protected from moisture and extreme temperatures. Shipping documentation includes safety data sheets (SDS), and transport is arranged via regulated carriers for hazardous substances. |
| Storage | Store 1-Hexyl-2,3-dimethylimidazolium bis((trifluoromethyl)sulfonyl)imide in a tightly-sealed container, in a cool, dry, and well-ventilated area, away from moisture, heat, and direct sunlight. Avoid contact with oxidizing agents. Handle under inert atmosphere if possible. Use appropriate personal protective equipment and ensure proper labeling. Keep container tightly closed when not in use to prevent contamination and degradation. |
Applications of 1-Hexyl-2,3-Dimethylimidazolium Bis((Trifluoromethyl)Sulfonyl)Imide in Industrial ManufacturingAs the direct manufacturer, we supply 1-Hexyl-2,3-Dimethylimidazolium Bis((Trifluoromethyl)Sulfonyl)Imide to a range of advanced industrial sectors, where its unique ionic liquid properties continue to enable measurable performance improvements, process safety, and formulation consistency. Our material finds application exclusively in process streams that demand high chemical purity, thermal stability, and electrochemical performance, as set out below for key downstream segments. 1. Electrolyte Additive for Lithium-ion and Sodium-ion BatteriesBattery cell producers leverage this ionic liquid to increase thermal stability, widen electrochemical windows, and decrease vapor pressure in advanced cells, specifically in pouch, cylindrical, and prismatic formats for electric vehicles and stationary storage. The additive integrates during the electrolyte preparation stage after vacuum drying, where it enables precise tuning of the electrolyte’s safety and cycling performance especially in high-voltage or high-temperature cells. Dosage varies according to cathode/anode chemistry, with rigorous internal QC to prevent metal-ion contamination and comply with global transportation battery regulations. Industry compliance standards
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2. Catalytic Reaction Medium for Organic SynthesisSeveral fine chemical plants employ this ionic liquid as a replacement for conventional volatile organic solvents (VOCs) in alkylation, acylation, and other transition-metal-catalyzed transformations, owing to its negligible vapor pressure and non-coordinating behavior. The additive supports sustained catalyst lifetime, reduces solvent waste, and simplifies downstream phase separation, all under GMP-compliant operation with validated remediation of ionic impurities in the isolation step. Industry compliance standards
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3. Antistatic Agent and Processing Aid in Engineering PlasticsPolymer compounders use this ionic liquid as a permanent antistatic agent during the melt extrusion of specialty engineering plastics such as polycarbonate, TPU, and PEEK, providing static dissipation without compromising optical clarity or mechanical strength. The incorporation method targets applications requiring compliance with strict ESD protection norms and low extractable ion profiles, especially in electronics packaging, medical devices, and automotive interiors. Industry compliance standards
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4. Solvent and Conductive Diluent in Electrochemical SensorsSensor manufacturers employ this ionic liquid as an inert, ion-conductive diluent or bulk solvent within potentiometric and amperometric sensor devices, offering high chemical resistance and low background current. It assists in the formulation of ion-selective membranes or gel polymer electrolytes, typically introduced prior to membrane casting or electrode assembly under cleanroom manufacturing protocols. Quality control emphasizes batch-to-batch reproducibility and stability of electrochemical baseline under regulatory laboratory measurement requirements. Industry compliance standards
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5. Separating Medium in Metal Extraction and ElectrowinningMajor hydrometallurgical operations utilize this ionic liquid to enhance selectivity and efficiency in liquid–liquid extraction and electrodeposition of rare earth elements, nickel, and cobalt. Its nonflammable and hydrophobic nature enables clear phase separation and stable chelation of metal ions, supporting operations in accordance with strict industrial environmental and worker safety codes. The raw material is loaded into extraction columns or mixer-settlers before phase contact and monitored for carry-over or degradation products during closed-loop processing. Industry compliance standards
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Our team at the plant wakes up every day to the smells and routines of chemical processing. We know it's not just about mixing the right feedstocks or counting liters. Success in our world hinges on discipline, experience, and transparent understanding. We introduce our 1-Hexyl-2,3-Dimethylimidazolium Bis((Trifluoromethyl)Sulfonyl)Imide, a mouthful on a label but a workhorse in real laboratory and industrial environments. This specific ionic liquid, known among chemists as [C6C1C1Im][NTf2], has left an impression on those pushing electrochemistry, extraction work, catalysis, and novel materials research past yesterday's boundaries.
Nobody in our factory gets away with shortcuts. Sourcing hexyl imidazole cores and engineered sulfonyl imide reagents means each batch lands in a place we have controlled from raw material to final seal. The journey for our 1-hexyl-2,3-dimethylimidazolium bis((trifluoromethyl)sulfonyl)imide often starts in a flask, watched by operators with the authority to halt production if clarity, purity, or reactivity falls below our standards. You might think every ionic liquid is just a solvent with unusual properties, but that's a shallow view.
The hexyl chain isn’t a frill on an otherwise standard imidazolium cation. Our technicians have seen variant after variant in side-by-side testing. Swapping out shorter chains or tinkering with the methyl group positions causes measurable changes in miscibility and viscosity. While some shorter-chain analogs will give you lower viscosity, the hexyl tail grants this molecule a special tolerance for combining with both polar and non-polar guest molecules. In tough separations or as a medium for electrochemical cells, the difference jumps off the page. Customers running extraction units and battery R&D send us feedback that echoes what we see at our own bench: separating target solutes from complex mixtures and stabilizing sensitive catalysts hinges on these subtle cation modifications.
Solvent systems often live or die by their impurity levels. That’s not new to those slicing peaks off an NMR or checking conductivity profiles. In the factory, we obsess over color, odor, moisture, and trace metals because stray ions gum up high-performance applications. Drying steps, controlled-atmosphere handling, and repeated checks for halide and water residues shape our output. Chasing analytical-grade molecules is no small task: it chews up time, and labor, but keeps the trust of researchers who order directly from the people who make the batch.
Customers in the lab and on the shop floor hand us stories from their processes. Chemists isolating alkaloids or strategic metals like lithium cite process speed and yield stability traced to the non-coordinating NTf2 anion. Our own tests alongside these users point to a crucial fact: [C6C1C1Im][NTf2] resists chemical drift under thermal and electrical stress, where some more primitive, chloride-rich ionic liquids fail. That means you get less corrosion of equipment and lower contaminant bleed into product streams.
Some of the more exciting uses show up in areas like organic synthesis, where transition-metal-catalyzed reactions run hotter and more selectively in our ionic liquid than in conventional organic solvents. If you rely on catalyst particles from palladium or ruthenium, you’ll see less sintering and better recyclability, especially for air-sensitive processes. Recovery of valuable metals, be it from spent batteries or ores, is another segment where the true value of this compound cuts through marketing claims across the trading world. We see consistent extraction efficiency from feedback loops with industrial partners and small startups alike. That trust is earned through purity, not fancy brochures.
Battery developers, especially those working on lithium-ion and sodium-ion systems, draw a line between general-purpose solvents and what’s required for stable interfaces between electrode and electrolyte. Nobody wants to see dendrite formation or short circuiting, which can spell disaster in new battery architectures. Our 1-hexyl-2,3-dimethylimidazolium bis((trifluoromethyl)sulfonyl)imide supports wide electrochemical windows and maintains fluidity under both high and low voltage thresholds. That means faster transitions and fewer charging mishaps for next-generation batteries. The built-in thermal stability doesn’t just sit on a spec sheet—it lets researchers push further without spontaneous breakdown or dangerous byproducts.
Ultra-capacitor engineers and those studying ionic transport in flexible electronics also benefit from its sheer stability and conductivity. Switching out chloride- or phosphate-based alternatives for our NTf2-based liquid shows real improvements in operating lifespan, visible in repeated cycling tests on-site. It’s direct: fewer breakdowns and more repeatable results.
Industry engineers and scale-up specialists call, skeptical that each bottle will match the theoretical promise. They often cite batch-to-batch inconsistency elsewhere. We have written our own process controls and traceability mechanisms—our operators know the signatures of a clean batch, from color and flow properties to advanced spectroscopy checks. Quite a few of us worked in environments where vendors cut corners, blending downgrades in the name of cost or yield. In our facility, trust grows from honest reporting and responding to real setbacks.
Those running parallel comparisons with alternatives such as 1-butyl-3-methylimidazolium bis((trifluoromethyl)sulfonyl)imide often give us concrete reasons for switching to our hexyl-capped formulation. The C6 hexyl group changes the liquid’s physicochemical landscape. It translates to broader liquid-phase temperature ranges, expanded miscibility for extracting both organic and inorganic compounds, and steadier electrochemical performance. There’s no magic, just a re-engineered balance of bulk and flow.
We don’t need to listen only to ourselves. When researchers scaling amine or peptide separations call up and ask for another liter, they specify our NTf2-based ionic liquid because the actual phase separation lines up with what process design requires. Feedback from those working with rare earths and difficult hydrometallurgical extractions goes further: yields remain consistent over repeats, and secondary purification enjoys less interference. This isn’t soft praise—it keeps the lights on in their labs and ours.
Electroplating operations and analytical chemistry users demand ultra-low halide content. The vintage stories are the same: other sources leave contamination that spoils thin films or skews trace analyses. Our on-site QA involves rigorous ion chromatography and water Karl Fischer titrations. Operators recount stories of near-misses and problems in the field, which feed back to our line managers, driving new purity standards.
We don’t hide the challenges. No ionic liquid exists in a technical vacuum, and each carries weak points. Product age and atmospheric exposure impact hygroscopicity. If bottles are left open, moisture content eventually creeps up. We encourage closed-loop nitrogen-purged delivery for labs with severe sensitivity needs. Our team advocates for differential scanning calorimetry or impedance checks if you notice deviations, and we help troubleshoot based on real failures—not theoretical ones.
Shipping can expose the product to freeze-thaw cycles, especially in northern climates. Each transit risk involves clever packaging, but we coach clients on pre-use checks rather than making wild guarantees. If a batch absorbs water, we advise simple in-lab drying, but we remain prepared to replace legitimately compromised shipments. By self-auditing, we improve the final result.
We run findings from our QA teams straight into process adjustments. A few years back, a research group running lithium–sulfur cell experiments flagged a subtle conductivity drop-off in samples stored for extended periods. Our line workers and chemists traced the issue to a slight carrier solvent residue. Adjusting our washing and drying process, and verifying stability over extended timelines, has since driven down this failure mode. Neither higher-ups nor marketers issued this as a policy; the crew on the line owned it.
Our senior chemist, who’s spent decades driving process reactors and writing bench protocols, reminds the team: quality doesn’t come from ticking standard boxes. Each property—be it viscosity, hydrophobicity, or conductivity—demands constant attention. We respond to specific user calls: if a sector needs additional metal screening or alternate container types, we adjust.
Running multiple ionic liquid production streams, we've observed clear operational and usage differences among our formulations. Swapping 1-hexyl-2,3-dimethylimidazolium for butyl or methyl cousins affects miscibility with both water and organic phases. Our hexyl-based liquid shows a sharper preference for non-polar extractions, making it indispensable for isolating hydrophobic species. Viscosity edges slightly higher as the chain length grows, but this most often works to an application’s advantage—greater retention in extraction phases, better film formation in plating baths.
Anion swapping presents its own trade-offs. Some labs prefer tetrafluoroborate- or hexafluorophosphate-based liquids for niche reasons, citing cost or perceived reactivity. We remind those users that the bis((trifluoromethyl)sulfonyl)imide anion maintains higher chemical and thermal stability, and has shown over longer study to resist hydrolysis or decomposition, especially under harsh treatment—critical for those pushing the bounds of temperature and voltage.
Not every experiment calls for the full complexity of a C6 tail plus NTf2. Cost-conscious buyers sometimes lean toward simpler, lighter mixtures, particularly where volume outweighs specialty performance. We have fielded requests to customize cation or anion ratios, but many users circle back to the original after trial, because fringe simplicity rarely makes up for loss in long-term performance and reliability.
Making 1-hexyl-2,3-dimethylimidazolium bis((trifluoromethyl)sulfonyl)imide starts with a deep understanding of organic synthesis, washing, and purification. Our team sources not just feedstocks but upstream intermediates with known traceability. The quaternization and salt metathesis steps require finesse—water content and side reactions aren’t just head-office lines on a QA report, but concrete issues the floor crew watches for every single run. One faulty valve or miscalibrated temperature sends a batch awry, wasting resources and testing patience in the finishing room.
We have scrapped more batches than many outside the plant would believe, especially if color, smell, or purity deviates beyond our internal standards. Each step—wash phase, drying oven, final filtration—adds cost, but our plant leadership gives our operators clearance to reject anything less. These missed steps show up as disappointing performance at the user’s bench. So, every bottle we fill for a customer comes out of this environment: tight process control, responsive continuous improvement, and hands-on accountability from a crew whose expertise developed with the product line.
Ionic liquids sometimes serve as a green chemistry poster child. Our experience is more nuanced. Compared to volatile organic solvents, our [C6C1C1Im][NTf2] has negligible vapor pressure, reducing exposure for plant workers and customers handling open containers. That makes a real difference on the shop floor—noses confirm what the air samplers report.
Waste handling and downstream treatment show marked improvement, too. Traditional solvents often end up as hazardous waste, demanding active carbon or incineration cycles. Ionic liquids like ours resist volatilization and leaching. We manage residues from our own lines with internal recycling and, where possible, return drums for user-side recovery and reuse. These steps close loops and reduce regulatory headaches.
Care remains. Every team member who handles concentrated intermediates wears personal protection and double-checks all lines—our near-miss log proves diligence isn’t optional. Ferries of containers between lab, storage, and process lines operate under strict controls, overseen by shift leads trained up from within. Sustainability isn’t cheap slogans around here, but day-in-day-out commitment.
We treat product inquiries and troubleshooting calls as much more than transactions. Researchers running into odd results or scaling up for a pilot often supply clues for our continuous improvement teams. Suggestions for easier transfer systems, batch marking, or specialized compatibility checks drive our in-house progress. Those with custom solvent polarity needs or unique reaction design requirements occasionally inspire test batches. The best outcomes come from those who’ve worked with the real liquid in pressure, voltage, or extractive flows—collaboration, not isolation, moves the product line forward.
Experience shapes every stage of making and improving 1-hexyl-2,3-dimethylimidazolium bis((trifluoromethyl)sulfonyl)imide. Our operators carry pride in a well-run batch. The technical and practical knowledge we build doesn’t come from handbooks alone—it rises from real-world alignment with user needs and the lessons of every run. By sticking close to our users and driving open feedback into process adjustments, we carve out space for this specialty ionic liquid in processes that truly demand it. Tomorrow’s advances in extraction, energy, and synthesis will stem from this discipline and ongoing dialog.