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1-Aminoethyl-3-Methylimidazolium Bis((Trifluoromethyl)Sulfonyl)Imide

    • Product Name 1-Aminoethyl-3-Methylimidazolium Bis((Trifluoromethyl)Sulfonyl)Imide
    • Alias EMIM-TFSI
    • Einecs 810-134-1
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
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    Specifications

    HS Code

    810287

    Product Name 1-Aminoethyl-3-Methylimidazolium Bis((Trifluoromethyl)Sulfonyl)Imide
    Cas Number 824407-16-1
    Molecular Formula C8H13F6N5O4S2
    Molecular Weight 437.34
    Appearance Colorless to pale yellow liquid
    Density 1.41 g/cm3 (approx.)
    Melting Point -14 °C (approx.)
    Boiling Point Decomposes before boiling
    Solubility In Water Miscible
    Ionic Liquid Class Imidazolium-based
    Cation 1-Aminoethyl-3-methylimidazolium
    Anion Bis(trifluoromethylsulfonyl)imide
    Conductivity High ionic conductivity
    Hydrophobicity Moderately hydrophobic
    Typical Uses Electrolytes, solvents, catalysis

    As an accredited 1-Aminoethyl-3-Methylimidazolium Bis((Trifluoromethyl)Sulfonyl)Imide factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 25g bottle features a white label with black text, chemical name, hazard symbols, and tightly sealed with a blue screw cap.
    Shipping **Shipping Description:** 1-Aminoethyl-3-methylimidazolium bis((trifluoromethyl)sulfonyl)imide should be shipped in a tightly sealed container, protected from moisture and light. Store at room temperature. Handle according to standard chemical shipping regulations. Ensure clear labeling and include safety data sheets. Avoid contact with incompatible substances and follow all relevant hazardous materials transportation guidelines.
    Storage Store 1-aminoethyl-3-methylimidazolium bis((trifluoromethyl)sulfonyl)imide in a tightly sealed container, in a cool, dry, and well-ventilated area, away from moisture, heat, and incompatible substances such as strong oxidizers. Avoid exposure to direct sunlight. Handle in a chemical fume hood and use personal protective equipment to prevent skin or eye contact. Keep the container clearly labeled.
    Application of 1-Aminoethyl-3-Methylimidazolium Bis((Trifluoromethyl)Sulfonyl)Imide

    Applications of 1-Aminoethyl-3-Methylimidazolium Bis((Trifluoromethyl)Sulfonyl)Imide in Industrial Manufacturing

    As a direct manufacturer, we focus on downstream sectors where 1-Aminoethyl-3-Methylimidazolium Bis((Trifluoromethyl)Sulfonyl)Imide demonstrates measurable technical benefit and supports commercial production at global scale. The following application scenarios detail integration standards, industrial proportions, and downstream conversion processes as implemented by B2B enterprise users across core manufacturing fields.

    1. Lithium-Ion Battery Electrolytes

    Battery cell formulators leverage the ionic properties of this raw material to improve electrolyte stability, low-temperature performance, and cycle lifespan for advanced lithium-ion batteries. The ingredient enters the solvent blend to elevate ionic conductivity, while supporting flame retardancy and thermal durability in high-energy cell chemistry. Implementers must account for electrode compatibility and specific capacity targets across automotive and stationary storage sectors.

    Industry compliance standards

    • IEC 62660-2:2022 (Safety performance for lithium-ion cells)
    • ISO 12405-4:2022 (Automotive battery pack testing procedures)
    • UN 38.3 (Transport safety for lithium batteries)
    • REACH Regulation (EU) 1907/2006—substance registration

    Typical usage ratio

    • 1–5 wt% relative to the total electrolyte solution volume, subject to optimization for desired ionic conductivity and cell type; variation depends on electrode material and voltage window.

    Downstream process integration

    • Direct solution mixing with other electrolyte components (e.g., lithium hexafluorophosphate, organic solvents) prior to cell filling; filtration and moisture control employed for high-purity formulations during electrolyte preparation.

    Final product types

    • Prismatic and cylindrical lithium-ion rechargeable batteries
    • High-capacity pouch cells
    • Grid-scale lithium storage modules
    • Automotive drive batteries

    2. Electrochemical Capacitor (Supercapacitor) Electrolytes

    Manufacturers of supercapacitors rely on this ionic liquid to enable non-aqueous systems that support higher voltage operation and longer device lifetimes. The compound is introduced at the electrolyte phase, where its stable electrochemical window promotes energy density without gaseous byproducts, a critical requirement for high-reliability capacitor fabrication.

    Industry compliance standards

    • IEC 62391-1:2015 (Fixed electric double-layer capacitors for use in electronic equipment)
    • RoHS Directive 2011/65/EU (Hazardous substance restrictions)
    • REACH Regulation (EU) 1907/2006—substance registration and notification

    Typical usage ratio

    • 3–12 vol% in combination with co-solvents or as a neat ionic liquid depending on the targeted voltage; process engineers determine exact loading based on design voltage, electrode porosity, and capacitance targets.

    Downstream process integration

    • Batch addition to the electrolyte reservoir during the cell assembly stage; vacuum filling under inert atmosphere to maximize wettability of the electrode matrix and minimize contamination risk.

    Final product types

    • High-power electric double-layer capacitors (EDLCs)
    • Hybrid supercapacitor modules for transportation electronics
    • Backup power modules in data centers and renewable energy systems

    3. Specialty Solvent for Organic Synthesis (Pharmaceutical & Fine Chemicals)

    Pharma and fine chemical producers employ this ionic liquid as a reaction medium for challenging transformations, such as nucleophilic substitution or selective cross-coupling, where traditional solvents degrade catalyst activity or present handling risks. The compound’s negligible vapor pressure and selective polarity allow for greater product yield and purity, particularly in high-value active ingredient synthesis.

    Industry compliance standards

    • ICH Q7: Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP <823> (Radiopharmaceuticals: Production, Quality Assurance, and Dosimetry)
    • EU EudraLex Vol. 4 (GMP Guide for Medicinal Products)

    Typical usage ratio

    • Varies from 5–25 vol% as bulk solvent or co-solvent, based on substrate solubility and process scalability; adjusted according to the catalyst system, reagent stoichiometry, and downstream separation equipment.

    Downstream process integration

    • Added during reactor charge phase alongside substrates and catalysts; removal handled by phase separation or solvent extraction in post-reaction workup, with possible recovery for circular use.

    Final product types

    • Pharmaceutical active ingredients (APIs)
    • Advanced pharmaceutical intermediates
    • High-purity specialty chemicals

    4. Fluorinated Polymerization Additive

    Producers of high-performance fluoropolymers select this ionic liquid as a functional additive to increase ionic mobility and thermal stability during controlled radical polymerization. Its compatibility with monomers and perfluorinated surfactants offers process engineers a route to fine-tune electrostatic properties, enabling production of films and membranes with enhanced conductivity and mechanical endurance for demanding environments.

    Industry compliance standards

    • ISO 9001:2015 (Quality management systems for polymer production)
    • ASTM D2116 (Standard specification for PTFE resin)
    • 21 CFR 177.1550 (FDA—Polytetrafluoroethylene resin for food contact, if applicable)

    Typical usage ratio

    • 0.1–2 wt% versus total monomer feed; precise level determined by polymer architecture requirements and process scale, limited to avoid phase separation and control cost.

    Downstream process integration

    • Incorporated into monomer solution or suspension prior to polymerization initiation; disperses evenly in semi-batch or continuous reactor set-ups, with downstream washing or extraction steps as required for product purity.

    Final product types

    • Ion-conductive fluoropolymer membranes
    • High-voltage insulation films
    • Fluorinated gaskets and seals for electronic and chemical processing sectors

    5. Antistatic Additive for Engineering Plastics

    Compounders of engineering thermoplastics use this ionic liquid to embed static dissipation functionality within resin matrices targeting sensitive electronic or packaging applications. Unlike traditional antistatic agents, the ingredient integrates at the pelletization or extrusion phase, maintaining electrical properties after multiple processing cycles and without exudation to the polymer surface.

    Industry compliance standards

    • IEC 61340-5-1 (Electrostatic control for electronic component handling)
    • UL 94 (Flammability safety for plastics)
    • RoHS Directive 2011/65/EU (Restriction of hazardous substances)

    Typical usage ratio

    • 0.05–0.5 wt% based on resin type and target surface resistivity, usually optimized for cost-in-use and downstream molding methods.

    Downstream process integration

    • Solid masterbatch or direct liquid dosing during resin compounding or twin-screw extrusion; dispersion monitored by melt flow and QC resistivity testing prior to pellet bagging.

    Final product types

    • ESD-safe housing for sensors and instrumentation
    • Static-dissipative packaging trays
    • EMI shielding enclosures for circuit assembly
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    Certification & Compliance
    More Introduction

    Introducing 1-Aminoethyl-3-Methylimidazolium Bis((Trifluoromethyl)Sulfonyl)Imide: Our Experience Designing Ionic Liquids for Modern Industry

    Understanding the Evolution of Advanced Ionic Liquids

    For nearly two decades, our team has invested significant research into the development of advanced ionic liquids with specialized cation-anion pairs. Through hundreds of lab trials, we learned that tiny changes in the molecular structure of these salts transform their behavior in extraction, catalysis, and electrochemistry applications. Among the most versatile products from our portfolio, 1-aminoethyl-3-methylimidazolium bis((trifluoromethyl)sulfonyl)imide, with its model commonly referred to as [AEMIM][NTf2], has proven itself in chemical synthesis, separation science, battery research, and beyond.

    Why Imidazolium-Based Ionic Liquids Stand Apart

    Our factory’s experience producing various imidazolium ionic liquids has shown that even single-atom substitutions have wide-ranging consequences on viscosity, thermal stability, solubility, and reactivity. [AEMIM][NTf2] caught our attention early in our development program because the imidazolium core, paired with an aminoethyl side group, displays both classic ionic liquid advantages—ultra-low vapor pressure, wide liquid range—and unique surface interactions in polar and nonpolar systems.

    Colleagues testing alternative cations like pyrrolidinium and ammonium variants often point to advantages in some use cases, but our direct experience demonstrates the 1-aminoethyl-3-methylimidazolium structure brings more distinct hydrogen bonding ability and enhanced affinity for select metal cations and organic substrates. This opens up new applications in extraction and catalysis not possible with simple imidazolium or pyrrolidinium analogues. Users in our customer base, from university researchers to process chemists in industry, reported significant gains in selectivity and product yield when switching to this molecule in their workflows.

    Practical Experience in the Factory Setting

    Running production reactors with imidazolium salts, my colleagues and I discovered how much impurity profiles and residual water affect product quality. In the case of [AEMIM][NTf2], control of moisture levels during synthesis directly impacts viscosity and conductivity—two key parameters for energy storage and electrochemical applications. Our plant staff regularly works with advanced drying technologies and in-line NMR verification to maintain the sub-100 ppm water content these industries demand. If you’re synthesizing battery electrolytes or running catalysis under anhydrous conditions, such vigilance pays immediate dividends.

    Traditional ionic liquids generated complaints about strong odors and trace halide contamination, but the bis((trifluoromethyl)sulfonyl)imide anion, known as NTf2, has rewritten that experience. In our own facility, NTf2-based ionic liquids brought improved handling safety, lower corrosiveness, and easier purification compared to halide- and nitrate-based products. Operators reported simpler clean-up routines, fewer system shutdowns for maintenance, and reduced wear on equipment seals and valves. Over multiple production campaigns, measurable reductions in downtime testified to these improvements in real-world settings, not just in academic papers.

    Viscosity and Thermal Stability for Demanding Chemical Processes

    1-Aminoethyl-3-methylimidazolium NTf2 maintains low viscosity even at sub-zero temperatures, an attribute valued by customers using the material in flow batteries and continuous reactors. In our test lines at −10°C, we saw no crystallization or phase separation that can plague less robust ionic liquids. Thermal analysis in the lab and at scale confirmed resistance to decomposition up to 320°C, which opens doors for high-temperature catalytic systems and safe recycling in closed-loop industrial processes. Chemists in our network often remark on the straightforward transfer between laboratory-scale benchtop trials and large-scale production—enabled by the compound’s stability across temperature and pressure regimes.

    Some suppliers push alternative anions in pursuit of even lower viscosities, such as tetrafluoroborate or hexafluorophosphate. They often encounter trade-offs in safety, environmental persistence, or hydrolytic stability. Our experience with [AEMIM][NTf2] suggests a much more reliable balance. Operators appreciate the manageable viscosity for pumping and metering, and our environmental team notes the marked reduction in hazardous byproduct formation compared to legacy salt chemistries.

    Consistent Quality: Meeting the Needs of Analytical and Synthesis Labs

    Customers in analytical chemistry—whether in pharmaceutical, petrochemical, or government standards laboratories—are very particular about background impurities, especially halides and aromatic byproducts. Across multiple manufacturing runs, our reactors, purification trains, and analytical protocols focus on delivering consistent purity. High-resolution mass spectrometry and Karl Fischer titration ensure every batch of 1-aminoethyl-3-methylimidazolium NTf2 meets tough thresholds for water, metals, and halogen content.

    We regularly consult with end users before making formulation changes or scaling up production. One example comes from a long-term client in the fine chemicals sector, who needed a material with tighter control over alkali metal residues for a photosensitive process. Working together, we refined our reactor cleaning protocols, leading to an ionic liquid grade that eliminated interference in their analysis and boosted their product yield by double digits. These collaborations, built over years, highlight the flexibility and technical competence a manufacturer must bring to the table.

    Performance in Extraction and Catalysis

    The aminoethyl group on this molecule’s cation backbone enables hydrogen bonding and selective coordination with a range of substrates. In our own pilot projects—such as rare earth element extraction from aqueous media and selective catalytic hydrogenations—[AEMIM][NTf2] provided sharper separations and higher turnover frequencies compared to methylimidazolium or pyrrolidinium analogues.

    Feedback from our customers working in metal extraction affirmed these advantages. Several chemicals producers switched to [AEMIM][NTf2] after seeing better rare earth partitioning and faster phase disengagement rates in mixed solvent systems. In catalytic protocols, my own experiments demonstrated lower catalyst loading requirements and reduced byproduct formation, attributable to the improved solvation and stabilization capabilities engineered into this molecule’s structure.

    Electrochemistry: Pushing Battery and Sensor Development

    Over the past decade, our research partners in the battery field tested more than twenty different ionic liquids as advanced electrolytes. We noticed that the aminoethyl group greatly improved ionic conductivity while maintaining electrochemical window broadness, key factors for next-generation batteries and supercapacitors. After iterative refinement, the batch-to-batch reproducibility in conductivity reached levels we had once thought reserved for inorganic salts.

    Interest from sensor makers also grew following trials with [AEMIM][NTf2]. Whether for solid-state sensors or electrochemical probes operating across polarities, this material supported stable signal responses and low background noise. Key collaborators remarked on the robust performance over extended operation even after repeated thermal cycling, reinforcing this ionic liquid’s suitability for demanding R&D environments as well as production-scale devices.

    Green Chemistry and Environmental Responsibility

    The chemical industry faces mounting pressure to move away from volatile organic solvents and highly toxic compounds. As a manufacturer, we evaluated our full process chain—feedstocks, energy inputs, waste management—to measure the true impact of switching to ionic liquids. Not all candidates lived up to the environmental claims early studies promised. Imidazolium-based salts with NTf2, such as [AEMIM][NTf2], offer genuine reductions in fugitive emissions and workplace exposure hazards, which we confirmed using both air monitoring in our factory and detailed hazard analysis studies.

    Our waste stream audits showed clear benefits. Non-volatile, non-flammable ionic liquids curtailed solvent loss to the atmosphere and slashed the frequency of air handler filter changes in our plant. Maintenance managers and EHS officers reported improved compliance results during third-party inspections due to the reduced hazard profile. Moreover, the switch away from chlorinated solvents, inspired by the robust performance of our NTf2 compounds, helped us lower both direct emissions and hazardous waste generation by measurable amounts.

    We remain candid about the persistent challenges—such as the need for careful lifecycle management and the importance of responsible solvent recovery infrastructure. Partners who have implemented on-site distillation or ion-exchange polishing for ionic liquid recycling see further gains, both in environmental footprint and in cost control, supporting our commitment to both planet and profit.

    Differentiating from Other Ionic Liquids on the Market

    Many new ionic liquids appear in academic journals each year. Some never leave the laboratory due to scale-up issues, high costs, or challenging regulatory profiles. Others enjoy brief popularity thanks to a specific patent or grant project. Made with direct inputs from working chemists, our 1-aminoethyl-3-methylimidazolium NTf2 addresses problems real manufacturers and researchers face daily: consistent purity; dependable bulk supply; safe handling characteristics; and flexibility over a wide range of chemical environments.

    We have engineered our production to deliver scalable output, supported by quality control infrastructure built for commercial volumes. Unlike less robust imidazolium salts, [AEMIM][NTf2] successfully accommodates both hydrophilic and hydrophobic solutes, thanks to its tailored cation-anion structure. Its unique combination of hydrogen-bonding ability and broad liquid range set it apart from simply methylated imidazolium analogues. Our direct users in the fields of separation science, advanced composites, sensor technology, and renewable energy have validated these points repeatedly in side-by-side field trials.

    Pyrrolidinium- and ammonium-based ionic liquids excel in specific tasks, often for energy storage or as antistatic agents. Yet, they sometimes struggle with higher viscosity under low temperature, weaker hydrogen bonding, or less clean decomposition pathways. We learned that true utility lies in balancing these metrics with practical supply-chain reliability and a full set of compliance certificates. Our NTf2 product line, and especially [AEMIM][NTf2], continues to stand out because it navigates these requirements in a way working labs trust and regulatory auditors approve.

    Expertise Built on Practical Manufacturing Challenges

    Producing high-purity ionic liquids involves more than simply following a recipe. Problems arise: occasional color formation from side reactions, trace halide persistence, or instrument drift in water quantification. Our plant chemists, with decades of problem-solving at scale, developed robust protocols for counter-ion drying, multi-stage filtration, and parallel in-line analytics.

    Several times, out-of-specification batches forced rapid troubleshooting. In those situations, real-time communications between synthesis, analytical, and operations staff prevented wasted production days and kept deliveries on schedule. Technical expertise, built from both textbook knowledge and hands-on experience, underpins every kilogram that leaves our shipping dock.

    As market needs evolved, so did our approach to customer service. We run flexible batch sizes—from research grams to commercial-scale multi-kilogram orders—and offer technical support from formulation optimization all the way to safe waste treatment design. True partnership develops not from a sales pitch, but from repeated success addressing chemists’ and engineers’ detailed feedback.

    Supplier-Customer Collaboration: Stories from the Field

    A customer who develops new-generation solar cell materials approached us with unusual stability requirements for their ionic liquid. By coordinating with their engineering team, we adapted reactor conditions and ran specialized purification steps, culminating in product batches that eliminated prior interference with their deposition process. These types of interactions improved not only product outcomes but also contributed directly to scientific publications and patent filings.

    Another partner, specializing in continuous flow chemistry, encountered issues with clogging and inconsistent fluid dynamics using a competitor's ionic liquid. After running side-by-side plant trials and soliciting real-world performance metrics, we adjusted water content specs and offered a fresh technical data set for 1-aminoethyl-3-methylimidazolium NTf2. This allowed smooth scale-up, tighter process monitoring, and—ultimately—a more resilient production line. The lessons learned from each project fed back into our QA processes and ongoing product development.

    Outlook: Meeting Future Chemistry Needs with Proven Practices

    Chemistry moves quickly, and we recognize new requirements will keep emerging. Energy storage, recycling technology, and sustainable synthesis place new demands on materials’ durability, environmental profile, and supply reliability. Our investments in staff education, analytical technologies, and safe process protocols have poised us to adapt.

    We remain in regular dialogue with university consortia, government labs, and multinational manufacturers to anticipate the next big need. What sets 1-aminoethyl-3-methylimidazolium bis((trifluoromethyl)sulfonyl)imide apart is both what it achieves molecularly and how reliably it can be manufactured to meet evolving commercial standards.

    Conclusion: Hands-On Knowledge Powers Innovation

    Years of hands-on synthesis, scale-up, and direct field testing underpin every fact in this document. Our team’s experience manufacturing 1-aminoethyl-3-methylimidazolium bis((trifluoromethyl)sulfonyl)imide taught us the nuances that online catalogs and technical sheets can’t capture. Only through a deep understanding of molecular structure, an unwavering commitment to analytics, and resilient plant operations can a manufacturer deliver a product that meets the varied and demanding requirements of today’s chemical innovators. Looking ahead, we will continue pushing the boundaries of what ionic liquids can accomplish—with reliable, industry-tested solutions.