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HS Code |
664159 |
| Chemical Name | 1-Hydroxyethyl-3-Methylimidazolium Trifluoromethanesulfonate |
| Cas Number | 944171-65-3 |
| Molecular Formula | C7H11F3N2O4S |
| Molecular Weight | 292.23 g/mol |
| Appearance | Colorless to pale yellow liquid |
| Melting Point | - |
| Boiling Point | - |
| Density | 1.41 g/cm3 (at 25°C) |
| Solubility | Miscible with water |
| Purity | Typically ≥98% |
| Ionic Liquid | Yes |
| Ph | Neutral to slightly acidic (in aqueous solution) |
| Smiles | CC1=CN=CN1CCO.OS(=O)(=O)C(F)(F)F |
| Inchi Key | QFZALPTENRRTSA-UHFFFAOYSA-N |
| Refractive Index | 1.425 (at 20°C) |
As an accredited 1-Hydroxyethyl-3-Methylimidazolium Trifluoromethanesulfonate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 500g of 1-Hydroxyethyl-3-Methylimidazolium Trifluoromethanesulfonate is securely sealed in an amber glass bottle with tamper-evident cap. |
| Shipping | 1-Hydroxyethyl-3-methylimidazolium trifluoromethanesulfonate is typically shipped in tightly sealed, chemical-resistant containers to prevent moisture absorption and contamination. It should be transported in compliance with local and international chemical transport regulations, away from incompatible materials, and stored at room temperature. Proper labeling and documentation must accompany the shipment for safety and regulatory compliance. |
| Storage | Store 1-Hydroxyethyl-3-Methylimidazolium Trifluoromethanesulfonate in a tightly sealed container, away from moisture and incompatible substances such as strong oxidizers. Keep in a cool, dry, and well-ventilated area. Protect from direct sunlight and heat sources. Clearly label the container and ensure suitable secondary containment in case of leaks or spills. Follow all relevant safety and chemical storage guidelines. |
Applications of 1-Hydroxyethyl-3-Methylimidazolium Trifluoromethanesulfonate in Industrial ManufacturingAs a direct manufacturer specializing in ionic liquid synthesis and supply, we have observed 1-hydroxyethyl-3-methylimidazolium trifluoromethanesulfonate’s adoption across specific high-value industrial settings. This material’s distinct conductivity, chemical stability, and solvation properties enable process improvements and product quality enhancements within advanced manufacturing sectors. Below, we detail several validated downstream applications, each with scenario-specific regulatory, formulation, processing, and end-product information based on real-world industrial operations. 1. Electrochemical Capacitor ElectrolytesThis ionic liquid serves as a non-flammable, high-voltage electrolyte in the assembly of supercapacitors and electrochemical double-layer capacitors (EDLCs). Integrators select it for its broad electrochemical window and thermal stability, supporting device cycles in demanding environments. Material enters the electrolyte mixture preparation stage, where rigorous control over water content and ion composition is critical to final device reliability. Industry compliance standards
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2. Lithium Battery Electrolyte AdditiveIn next-generation lithium battery cells, this ionic liquid functions as a non-volatile co-solvent or additive, improving ion conductivity while reducing the risk of dendrite growth. The raw material typically mixes with carbonate solvents and lithium salts, enhancing cell lifespan and safety in advanced rechargeable battery platforms. Industry compliance standards
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3. Biomass Dissolution for Cellulose ProcessingThis ionic liquid sees application in biomass valorization processes, particularly in the efficient dissolution and fractionation of lignocellulosic materials such as wood pulp and agricultural waste. Its strong hydrogen-bond accepting ability allows for direct dissolution of cellulose, preceding enzymatic saccharification or regeneration into structured films and fibers. Manufacturers optimize the liquid’s inclusion to balance cellulose recovery with solvent recyclability. Industry compliance standards
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4. Homogeneous Organometallic Catalysis MediaCatalysis process engineers employ this ionic liquid as a reaction solvent or phase transfer medium to enhance solubility and selectivity in transition metal-catalyzed transformations—such as alkylation, Suzuki-Miyaura coupling, and olefin metathesis synthesizing pharmaceutical, specialty, and agrochemical intermediates. Its high polarity, chemical inertia towards most catalytic metals, and recyclability underpin cost-efficient batch or continuous processes. Industry compliance standards
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5. Metal Electrodeposition and Surface FinishingThis ionic liquid is implemented in electrolytic deposition baths, offering enhanced metal ion mobility, low volatility, and increased uniformity compared to aqueous or traditional organic bath systems. Applications target the fine plating of gold, silver, and nickel on microelectronic contacts and other precision components where dimensional accuracy and surface quality remain paramount. Operators carefully monitor bath composition and impurity control during continuous operation. Industry compliance standards
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Every year, chemists demand more from ionic liquids, especially in fields like catalysis, electrochemistry, material synthesis, and separations. Among the large families of imidazolium-based ionic liquids, 1-hydroxyethyl-3-methylimidazolium trifluoromethanesulfonate has proven reliable both in our own production facilities and through collaborations with research institutions. The unique cation-anion pair promises stability, broad chemical compatibility, and ease in scaling up or down for laboratory and industrial requirements.
We manufacture 1-hydroxyethyl-3-methylimidazolium trifluoromethanesulfonate under controlled temperature and pressure, with every batch monitored at critical synthesis steps. The process uses high-purity starting materials. Our standard model achieves water content below 0.5% by Karl Fischer titration. Each lot includes a specification sheet detailing residual halides, metallic impurities, and anion content, which we confirm through ion chromatography.
Our ionic liquid shows a colorless to pale yellow appearance in its pure form and pours easily at room temperature. The product demonstrates high thermal stability; decomposition does not begin until above 300°C. Conductivity measures consistently in the desired range for typical ionic liquids, and viscosity matches published values. Shelf life extends to several years under proper storage, and the ionic liquid tolerates exposure to air and minimum light without noticeable degradation, based on accelerated aging tests performed at our site.
The growing field of green chemistry requires solvents that do not evaporate, combust easily, or react unpredictably. Our 1-hydroxyethyl-3-methylimidazolium trifluoromethanesulfonate fills a gap for a hydrophilic ionic liquid that carries a strong trifluoromethanesulfonate anion, enhancing both chemical and thermal resilience. The hydroxyethyl group on the cation introduces moderate hydrophilicity, giving the liquid good solubility in water and polar organic solvents, while still allowing for ionic interactions essential in many catalytic cycles. Synthetic chemists who aim to reduce volatile organic compound emissions have found this material to be a direct substitute in many dissolution, extraction, and reaction media tasks, allowing clean workups and recycling.
Electrochemists look for electrolytes with wide electrochemical windows and high ionic conductivity. Our ionic liquid’s compatibility with a broad range of redox couples makes it appealing for electroplating, batteries, supercapacitor work, and sensor material development. Colleagues in the material sciences have reported success in templating, sol-gel processing, and nanoparticle stabilization, confirming its gentle interaction with sensitive precursors while resisting side-reactions that occur with less stable ionic liquids.
Early in our development program, pharmaceutical partnerships raised concerns about purity for advanced synthetic steps involving organometallic intermediates. Our experience optimizing purification and repetitive testing enabled consistent delivery of spectral-grade product. For advanced organic synthesis, users appreciate the mild basicity and low nucleophilicity of the trifluoromethanesulfonate anion, which suppresses unwanted side products and aids in selectivity.
Continuous feedback from end users, process engineers, and academic groups has shaped both our process development and product scope. In the world of imidazolium-based ionic liquids, small changes in cation or anion structure drive big differences in application. The hydroxyethyl group on the imidazolium ring shifts this liquid away from more traditional alkyl-imidazolium salts, such as 1-butyl-3-methylimidazolium or 1-ethyl-3-methylimidazolium. While these older versions emphasize lipophilicity and compatibility with nonpolar media, our hydroxyethyl functionalization brings more miscibility with aqueous and highly polar environments.
The trifluoromethanesulfonate anion offers unique benefits over alternatives like PF6, BF4, or NTf2. PF6 and BF4 carry the risk of slow hydrolysis, releasing undesirable byproducts, especially when exposed to ambient moisture. In contrast, trifluoromethanesulfonate remains stable under similar conditions, eliminating many headaches for those working outside strictly controlled glovebox environments. The triflimide anion (NTf2) does grant low viscosity and hydrophobicity, but it comes with synthetic complexity and cost. Our ionic liquid, with its triflate anion, strikes a better balance between price, ease of use, and environmental persistence.
For those switching from conventional volatile organic solvents, the reduction in vapor pressure brings safety benefits. No significant odor or fume forms during standard handling, and ignition risks lower dramatically versus ethers or hydrocarbons. We’ve seen several firms safely transition their pilot plant setups to ionic medium-based routes, reducing solvent emissions and exposure-related incidents.
Users processing large volumes have noted our process minimizes formation of halide byproducts. Many halogen-containing ionic liquids require time-consuming purification or repeated extractions, contributing to operational delays and extra waste. By controlling halide content during every synthesis, the end product offers predictable performance across many chemical transformations or separation steps.
Feedback from workers handling the product in both lab and plant settings has guided us to optimize bottle sizes, closures, and safety labeling. The liquid pours well at ambient temperatures, without sticking or forming crystalline byproducts. Workers report easy rinsing and less stubborn residue when compared with more viscous or unstable ionic liquids. Containers keep integrity during long-term storage, provided they remain sealed and away from direct sunlight.
Spills and splashes, though rare due to the liquid’s low volatility, clean up using standard absorbents. The chemical’s thermal and chemical inertness toward glass, stainless steel, and high-grade plastics simplifies equipment cleaning steps. Waste minimization and disposal align with local protocols, as no reactive or bioaccumulative contaminants form under standard processing and hygiene conditions.
Several academic and industrial research publications describe the use of 1-hydroxyethyl-3-methylimidazolium trifluoromethanesulfonate as a green alternative in organic synthesis pathways. These papers highlight improved yields, product purities, and reduced energy consumption, especially in microwave-assisted or solvent-free transformations. We have worked directly with university teams eager to test solvent systems that can recycle efficiently. Recovery of both solute and ionic liquid has allowed partner labs to operate at reduced cost and lower environmental impact over repeated cycles.
A notable example emerged from a multi-year collaboration with a battery materials manufacturer. The end user sought an electrolyte that tolerated high potentials without decomposing and that did not corrode aluminum or copper current collectors. Integration testing over hundreds of cycles showed minimal change in the physical or electrochemical profile, extending device life and cutting replacement frequency. Such real-world results matter more than theoretical projections.
In catalysts research, several groups replaced conventional dipolar aprotic solvents with our ionic liquid. Reaction times shortened, solid yields increased, and emissions dropped, as recorded by third-party audits. Reactor fouling and maintenance intervals grew less common, which lowered costs in the long run. These case studies reinforce that adoption owes as much to practical operation as to published chemical properties.
Some buyers care mainly about purity; others demand reliability batch-to-batch. Over two decades producing ionic liquids, we have learned that these requirements go hand-in-hand. Long before independent audits required them, we implemented in-line controls, regular cross-checks, and multiple analytic endpoints on every batch. FTIR, NMR, and mass spectrometry records follow every lot out the door, corrected for background and blind controls from every shift.
We recognize that shelf chemistry evolves, especially when large volumes or long-term supply contracts shape the relationship. Learnings from the field flow directly into process review and revalidation cycles. Recent feedback led to investment in additional chromatographic separation for further reduction of trace side-products, and blind retrials on legacy production lines have kept cross-contamination to a minimum.
Resilience during scale-up matters as much as theoretical efficiency. Even small scale syntheses impose unexpectedly high material costs or waste streams when handled at the kilogram or larger scale. Dialogue with buyers, from postdoc to process manager, adds crucial context each year, guiding both incremental improvements and big process overhauls.
Chemicals built for green and sustainable transformations deserve attention not just at point-of-use, but across the production and stewardship chain. The hydroxyethyl group derives from routinely available feedstocks, and the synthesis steps do not call for rare or highly toxic reagents. Byproduct formation falls within manageable ranges during standard plant operations, and we recycle solvents and catalyst beds wherever possible.
Our workplace safety protocol includes regular hazard reviews, spill drills, and personal protective equipment training. The low hazard classification and high flashpoint allow more flexibility for storage and in-processing. This sets our offering apart from ionic liquids containing halide or hexafluorophosphate anions, which can react seriously with ambient moisture or heat.
For customers operating in sensitive environments—such as pharmaceutical cleanrooms or electronics assembly lines—the ionic liquid’s low outgassing, low residue, and non-corrosive properties align with high workplace standards. Disposal routines fit within existing chemical protocols and do not require difficult tracking or exotic neutralization steps.
Widespread adoption of new ionic liquids depends on more than headline properties or catalog entries. Production scale can bring unexpected hurdles—impurity control, shipping stability, regulatory acceptance, and cost optimization. Our on-site team faces the challenge of balancing purity, speed, and price every cycle, especially as demand continues to climb in emerging applications like advanced polymers and pharmaceutical ingredients.
Shipping logistics, especially for international buyers, encouraged us to diversify packaging, insulation, and customs documentation. We have adjusted material compatibility after seeing rare reactions with an older batch of stoppers or liners. A transparent system of lot records, quality testing, and feedback ensures every drum, bottle, and sample reflects the latest standards and oversight.
To support researchers in smaller labs, we maintain a sample program allowing access to small-scale lots for method development. If special analytic tests become necessary, we coordinate either in-house or through certified partners. That way, students and seasoned professionals get the right information to compare performance side by side with familiar solvents.
As producers, responsibility extends past synthesis. Traceability requires more than tracking numbers—it depends on disciplined procedures and clear, continuous records. For every order, documentation matches physical product and analytic results, giving both new and returning users confidence in the material’s origin and consistency.
Consultation remains at the core of our engagement. Users’ process parameters, regulatory environments, and equipment may differ. Our technical staff maintains a regular dialogue with buyers, offering practical perspectives on best storage, in-use protocols, and safe handling. This hands-on approach saves time by solving issues before they grow, rather than enforcing generic or out-of-context guidelines.
From our early batches to each improvement milestone, real-world customer needs shape every aspect of 1-hydroxyethyl-3-methylimidazolium trifluoromethanesulfonate. New markets and research questions emerge each year, from antifouling coatings to solvent-free process development. We adapt both the chemistry and support structure to keep pace.
The unique traits of our ionic liquid—the careful choice of hydroxyethyl cation, the robust triflate anion, the emphasis on purity and process safety—bridge the needs of today’s chemists and tomorrow’s applications. Research teams, production chemists, and application engineers have all contributed insight to guide ongoing refinement. We welcome challenges that push the boundaries of what ionic liquids can do in practical, responsible, and sustainable ways.