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1-Carboxyethyl-3-Methylimidazolium Chloride

    • Product Name 1-Carboxyethyl-3-Methylimidazolium Chloride
    • Alias [C2mim]Cl
    • Einecs 829-444-0
    • 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

    208664

    Product Name 1-Carboxyethyl-3-Methylimidazolium Chloride
    Chemical Formula C7H11ClN2O2
    Molecular Weight 190.63 g/mol
    Appearance White to off-white solid
    Melting Point Approx. 80-120°C
    Solubility In Water Highly soluble
    Cas Number No widely assigned CAS; may vary by supplier
    Density Approx. 1.2 g/cm³ (at 25°C)
    Purity Typically ≥98%
    Storage Conditions Store in a cool, dry place; keep container tightly closed
    Boiling Point Decomposes before boiling
    Ph Value Approx. 5-7 (aqueous solution)
    Smiles CC(C(=O)O)N1C=CN=C1C.Cl

    As an accredited 1-Carboxyethyl-3-Methylimidazolium Chloride factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing White, sealed plastic bottle labeled “1-Carboxyethyl-3-Methylimidazolium Chloride, 100g” with CAS number, hazard pictograms, and QR code.
    Shipping **Shipping Description:** 1-Carboxyethyl-3-Methylimidazolium Chloride should be shipped in tightly sealed containers, protected from moisture and direct sunlight. Use secondary containment and clearly label packages. Transport under ambient conditions unless otherwise specified. Comply with local regulations for handling chemicals, and ensure compatibility with other cargo. Not regulated as hazardous for standard air and ground shipping.
    Storage 1-Carboxyethyl-3-Methylimidazolium Chloride should be stored in a tightly sealed container, in a cool, dry, well-ventilated area, away from incompatible substances such as strong acids and bases. Protect from moisture and direct sunlight. Store at room temperature and avoid excessive heat. Ensure proper labeling and access only by trained personnel. Follow all applicable safety guidelines and regulations.
    Application of 1-Carboxyethyl-3-Methylimidazolium Chloride

    Applications of 1-Carboxyethyl-3-Methylimidazolium Chloride in Industrial Manufacturing

    1-Carboxyethyl-3-Methylimidazolium Chloride, as an advanced ionic liquid, serves various industrial sectors that demand high selectivity, enhanced process efficiency, and reduced environmental impact. Based on long-term technical partnerships and downstream customer trials, we outline here the main industrial application scenarios verified in continuous or batch processes at scale.

    1. Cellulose Dissolution for Specialty Fiber Production

    Leading manufacturers of specialty cellulose fibers—including lyocell and microcrystalline cellulose—deploy 1-carboxyethyl-3-methylimidazolium chloride as a cellulose-dissolving medium, leveraging its remarkable hydrogen-bond disruption properties. This ionic liquid replaces conventional NMMO or caustic soda processes, primarily at the cellulose dissolution or spinning solution preparation step, greatly reducing the presence of secondary by-products and enabling higher molecular weight retention. Operators adapt the ionic liquid concentration to optimize fiber strength, fiber yield, and solvent recyclability within the spinning line.

    Industry compliance standards

    • OEKO-TEX® Standard 100 Certification for harmful substances
    • ISO 9001:2015 Quality Management for pulp and fiber
    • REACH Regulation (EC) No 1907/2006 for chemical substances in textiles
    • ZDHC Roadmap to Zero Chemical Management

    Typical usage ratio

    • 65–82% by weight in the solvent system, depending on cellulose purity and target fiber linear density. Higher ratios apply for microcrystalline and lower DP pulp grades.

    Downstream process integration

    • Added directly to pretreated pulp slurries in dissolution reactors and maintained in closed solvent cycles through the fiber extrusion, coagulation, and washing sequences. The material is recaptured and recycled on-site post-spinning.

    Final product types

    • High-tenacity lyocell fibers
    • Microcrystalline cellulose powders
    • Customized specialty cellulosic film grades for membrane production

    2. Lignocellulosic Biomass Fractionation in Biorefinery

    In integrated biorefinery operations, this ionic liquid operates as a tunable solvent phase, targeting delignification and fractionation of lignocellulosic biomass such as wheat straw, corn stover, and hardwood chips. The superior solubility profile results in clean fraction streams for downstream saccharification, fermentation, or catalytic conversion. Close attention is paid to residual ionic liquid removal, as this strongly impacts enzyme compatibility and final clarity in biofuel and biochemical stock production.

    Industry compliance standards

    • EN 16751:2016 Sustainability criteria for biobased products
    • ISCC PLUS Certification for sustainable bio-based processing
    • Industrial Biotechnology Environmental Standards (IBES), EU

    Typical usage ratio

    • 35–50% w/v in biomass processing solutions; adjustments depend on lignin content and particle size distribution.

    Downstream process integration

    • Charged in primary fractionation reactors after biomass grinding and mild aqueous pretreatment. Maintained under controlled temperature/pressure; reclaimed for reuse post-separation using antisolvent precipitation and vacuum filtration.

    Final product types

    • Bioethanol and second-generation biobutanol feedstock
    • Lignin isolates for phenolic resin or fuel pellet applications
    • Fermentable sugars for platform chemical synthesis

    3. Catalyst Support Phase in Homogeneous Catalysis

    Advanced homogeneous catalysis processes in the fine chemicals sector require ionic media that provide selective solvation of catalyst species and enhance turnover. 1-carboxyethyl-3-methylimidazolium chloride plays a direct role as a catalyst support solvent—particularly in carbonylation and alkylation systems—enabling catalyst recovery and reuse by modifying solvent/catalyst phase behavior. Its use reduces reliance on volatile organic solvents and boosts product purity by minimizing water and nonpolar impurities.

    Industry compliance standards

    • GMP Guidelines for Pharmaceutical Excipients (ICH Q7)
    • ISO 22716:2007 (Cosmetics—Good Manufacturing Practices) for formulations involving downstream APIs or cosmetic intermediates
    • European Pharmacopoeia (Ph. Eur.) for excipient residues, where applicable

    Typical usage ratio

    • 10–30% by mass of total solvent mix, depending on catalyst solubility and process temperature. Increased ratios favored in high-throughput flow reactors.

    Downstream process integration

    • Charged with catalyst precursor and reactants in jacketed batch reactors or continuously in flow-through columns. Acts as both solvent and catalyst-phase harvesting medium post-reaction, enabling easy phase separation.

    Final product types

    • Active pharmaceutical ingredients (API) intermediates
    • Agrochemical synthesis compounds
    • Specialty monomers and chemical building blocks for polymerization

    4. Electrolyte Additive in Novel Battery and Supercapacitor Manufacturing

    Producers of next-generation batteries and supercapacitors deploy 1-carboxyethyl-3-methylimidazolium chloride as a component or additive in advanced electrolyte formulations, seeking improved ionic conductivity, enhanced electrochemical stability, and non-flammability. The additive modifies ion transport characteristics and widens the operational temperature window, especially in high-voltage or high-capacity cell designs. Adjustments in its loading respond to cell architecture and separator compatibility requirements.

    Industry compliance standards

    • IEC 62660-1:2018 for secondary lithium cells and batteries
    • UN 38.3 testing for lithium battery shipping
    • RoHS Directive 2011/65/EU for hazardous material restrictions
    • SAE J2464:2009 for automotive battery safety

    Typical usage ratio

    • 3–14% by weight of electrolyte solution. Lower ratios apply in lithium-ion cells; upper range applies to hybrid supercapacitors.

    Downstream process integration

    • Mixed with standard electrolytes (such as LiPF6 or EMIM-based systems) at the electrolyte preparation stage, prior to vacuum filling and wetting in cell assembly lines. Remains in solution post cell-sealing.

    Final product types

    • Lithium-ion battery cells (high-voltage, low-flammability types)
    • Hybrid electrochemical capacitors
    • Energy storage device modules for consumer electronics and automotive markets

    5. Solvent System for Chitin and Derivative Extraction

    In crustacean exoskeleton processing lines, chitin and its derivatives gain from the use of this ionic liquid as an efficient solvent system. The high affinity for polysaccharide chains means a significant increase in extraction yields and reduced proteinaceous residue compared to traditional acid/base processes. Quality control laboratories see reproducibly higher chitosan degrees of deacetylation, and processing steps present lower environmental footprints thanks to closed-cycle solvent recovery systems.

    Industry compliance standards

    • ISO 22000:2018 Food Safety Management for food-grade chitosan
    • USP Monograph for Chitosan if marketed as dietary supplement
    • European Regulation (EC) No 1935/2004 for food contact materials

    Typical usage ratio

    • 40–60% w/w in extraction solvents, varying with raw material composition and target molecular weight of chitosan fractions.

    Downstream process integration

    • Applied after demineralization and deproteinization of shell waste. Introduction of the ionic liquid takes place during the main extraction heating phase, followed by aqueous precipitation of purified chitin/chitosan, with solvent reclaimed and purified on-site.

    Final product types

    • Medical-grade chitosan powders
    • High-purity chitin flakes for pharmaceutical and food industries
    • Biofilm-forming chitosan derivatives
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    Certification & Compliance
    More Introduction

    1-Carboxyethyl-3-Methylimidazolium Chloride: Practical Insights from Our Production Floor

    Making 1-Carboxyethyl-3-Methylimidazolium Chloride: What Drives Us as Producers

    At our factory, the process of producing 1-Carboxyethyl-3-Methylimidazolium Chloride demands a focus on both purity and consistency. Over many batches, we have found that minor shifts in raw material quality or reaction conditions can shape the end product in noticeable ways, influencing both the color and performance. Since this compound emerged in advanced ionic liquid research, demand from labs and R&D teams has grown steadily. The decision to refine our synthesis was not driven by hype or short-term trends. Instead, we responded to requests from industrial partners seeking ionic liquids with a wider window of thermal stability and a smoother, more predictable solvation capability.

    Our team recognized early that many customers grew frustrated with materials that came with a broad specification range for water content and impurity profiles. Some suppliers seemed content to operate near the threshold of acceptability, and that caused headaches in downstream catalysis or extraction work. We shifted our process towards tighter control—limiting impurity variations batch-to-batch, holding chloride content within a tighter window, and running more parallel testing for thermogravimetric and conductivity characteristics. As a result, our 1-carboxyethyl-3-methylimidazolium chloride now provides a reassuring degree of batch stability. Chemists who use this in multi-stage syntheses or pilot-scale separation projects have commented on how this stability saves time and helps avoid run-to-run surprises.

    Specifications Backed by Production Experience

    Many ionic liquids look similar on paper. If you flip through the literature, melting points, density, and solubility curves might seem to overlap. The real-world differences start showing up on the production line—factors like consistency of particle size, drying behavior, and resistance to color changes over time. Our in-house experience highlights these nuances. For instance, our batches typically display a pure white to very pale yellow color with negligible browning, even after several months of storage in sealed containers kept away from light and moisture. The water content remains below 0.1% due to vacuum drying at controlled temperatures. Conductivity measurements remain consistent within a narrow range, which pleases customers performing electrochemical applications or biphasic extractions.

    Often, customers ask about the cation and anion ratio. Our synthesis route yields a product with a narrow distribution in methylimidazolium purity and a strong correlation to chloride stoichiometry. Our analytic team runs regular NMR and IC tests to ensure both the cation and anion are present in the correct proportion. This matters in practical terms—for catalytic cycles using Lewis acids, too-broad anion spread can sabotage a whole batch, slowing down phase separation or fouling downstream filters. We learned the hard way, on our own pilot runs, that a slip in this area can force an entire rework of equipment cleaning, or even require new glassware. Keeping quality tight here is not a marketing boast—it’s a necessity learned through daily production challenges.

    Unique Features of 1-Carboxyethyl-3-Methylimidazolium Chloride

    Unlike more basic alkylimidazolium chlorides, adding a carboxyethyl group at the 1-position brings a new set of properties. This cation structure handles polar and non-polar compounds in unique ways, giving chemical engineers more flexibility during difficult separation or catalyst recycling steps. The extra carboxylic group adds hydrophilicity, which improves its performance in aqueous mixtures and makes extraction protocols more forgiving. Whereas some competitors’ products struggle to dissolve polar substrates, ours routinely stays clear and colorless in most laboratory solvents due to careful control in both synthesis and purification. Customers pursuing phase-transfer catalysis or ionic liquid membrane development often return to us because they experience lower contamination and fewer failed runs.

    Electrochemical consistency matters just as much as chemical purity. The cation-anion pairing in this structure supports a stable, wide electrochemical window. This opens up new routes for battery researchers and those working with electrodeposition or redox mediators. During our early trial batches, a few attempts using cheaper starting materials produced unexpected spikes of resistivity and off-odors. We documented every failed batch and traced the sources, finally accepting that small cost-cutting steps can bend the performance curve. Our established route now avoids cheap shortcuts, bringing end-users a liquid that behaves reliably from the test tube up to scale-up reactors.

    Direct Applications in Research and Industry

    From our regular conversations with users in the field, 1-carboxyethyl-3-methylimidazolium chloride wins favor for both process flexibility and reliability. In advanced solvent extraction scenarios, it remains stable even at elevated temperatures and high salt conditions, simplifying the process for separating target molecules from complex solutions. Compared to more basic imidazolium chlorides, it handles repeated heating and cooling cycles without significant breakdown or color drift. Customers working in pharmaceutical R&D often use it in chromatography columns or as a component for selective precipitation, where it maintains a steady solvation ability without promoting unwanted side reactions.

    In pilot-line catalyst recovery experiments, this ionic liquid’s tailored polarity helps streamline the capture and recycling of noble metals, such as platinum group elements. Users have reported that our batches provide clear advantages in metal ion retention, saving on both material and time, especially in continuous-flow systems. Academic partners pursuing green chemistry routes incorporate it as both a reaction medium and a phase-transfer reagent, due to reduced volatility and lower environmental load compared to organic solvents. During feedback sessions, a recurring theme is the savings in solvent exchange time, and a noticeable drop in the cleaning cycles needed between production runs.

    Electrochemists appreciate the stable conductance profile, finding it well-suited for both fundamental redox studies and prototype cell construction. Unlike less refined alternatives, our material contains minimal organic and inorganic contaminants, helping researchers control for background interference in cyclic voltammetry and impedance spectroscopy. These details might sound minor, but in real practice, impurities create hours (or days) of troubleshooting. By tightening our spec and offering documentation on each batch, we help labs spend more time on their own work, not on material re-qualification.

    Comparing Our Product to Other Ionic Liquids

    Ionic liquids as a class offer large structural variety, but not every option stands up to the same performance yardstick. Many competitors still use a “one-size-fits-all” mentality, shipping generic imidazolium chlorides with varying levels of unreacted precursor or water. For teams scaling up to kilo-level syntheses or pilot plant research, these details add up. Our 1-carboxyethyl-3-methylimidazolium chloride is produced in-house from carefully selected precursors. Unlike standard 1-alkyl-3-methylimidazolium salts, our addition of a carboxyethyl chain tampers down volatility, especially at higher temperatures. This supports longer process runs and greater safety margins for downstream concentration or recycling.

    Our experience shows that while tetrafluoroborate or hexafluorophosphate analogs deliver comparable ionic conductivity in some cases, they bring different risk profiles. For instance, they can hydrolyze to release toxic or corrosive side products over time, especially under ambient moisture. Chloride-based ionic liquids avoid these pitfalls and streamline waste management, since disposal and neutralization require less aggressive protocols. In our own plant, switching to chloride-based options reduced our environmental compliance paperwork and simplified routine maintenance. Feedback from colleagues at other production sites confirms these points, with many reporting fewer filter clogs and easier tank cleaning with chloride salts.

    Addressing Market Expectations and Real-World Pain Points

    Several years ago, we started noticing a shift: end-users became less interested in “exotic” salts with unpredictable shelf-life or performance. More buyers instead wanted dependable results and documentation, enabling them to replicate data again and again. Our development team made it a priority to focus not just on specs, but on providing supporting information for every batch—moisture analysis, NMR traceability, thermal stability charts, and impurity scans. This investment reduces confusion for the researchers and engineers who depend on us for both accuracy and speed. For example, if a batch’s water content strays too high or if a byproduct begins to creep up, we halt release and communicate the issue, saving everyone time and resources down the line.

    Research teams often work under tight grant deadlines. An unexpected material deviation, such as a spike in ionic conductivity or a small color change after heating, can waste weeks of work. Our goal is to remove these headaches by running additional testing stages and by maintaining open lines of discussion with our key users. This approach has built a reliable relationship that extends well beyond standard chemical supply.

    Application Highlights from the Field

    Across our user base, several cutting-edge projects highlight what makes our 1-carboxyethyl-3-methylimidazolium chloride stand apart. For example, several pharmaceutical startups integrate this compound into new purification schemes for chiral intermediates. The ionic liquid’s unique polarity improves the separation of closely related isomers—increasing the yield and purity of the end product. In direct conversations, process engineers describe easier scale-up with our material because the solution phase remains stable through repeated cycles, even when starting materials bring more water or organic impurities.

    Materials scientists working on energy storage and next-generation capacitor technologies use it as both electrolyte and process aid. Because our chloride salt keeps a reliable performance profile, researchers avoid the step of retraining sensors or recalibrating test equipment with each shipment. They have cited improved reproducibility in electrochemical cycling and better compatibility with emerging electrodes.

    Green chemistry projects, especially those aiming to cut down on hazardous solvents, have shown strong preference for carboxyethyl-3-methylimidazolium chloride. Many labs mention its easy phase separation with aqueous mixtures, faster reaction times, and lower volatility. Several have published work showing that it enables new catalytic transformations that would be too difficult or risky in traditional solvents. Our direct input during scale-up and troubleshooting has helped resolve persistent challenges, such as tank residue or downstream fouling, by tailoring cleaning and recovery protocols to the exact properties of our material.

    Improvements Driven by On-Site Feedback

    Most improvements in our production did not come from the boardroom or market trends but from worker input on the plant floor. Each time a batch presented an unexpected result—be it a slight color shift, an increase in viscosity, or slower dissolution—a few hours would go into troubleshooting. Sometimes the root cause lay in a supplier’s change to a base material; other times, the solution came from tweaking vacuum drying conditions or fine-tuning filtration steps. We have learned not to underestimate the value of hands-on knowledge and close loop communication from synthesis to final packaging.

    Training new technicians includes not just the “how-to” of making a good batch, but specific checks on every lot. Rather than trusting paperwork alone, we emphasize physical testing: heating a sample, watching it dissolve, measuring conductivity, and even noting how the bulk product smells and handles compared to previous batches. These routine steps help us catch problems before they reach customers and keep quality improvements moving in the right direction.

    Sustainability and Safety Benefits from the Production Lens

    Chloride-based ionic liquids, including our carboxyethyl-methylimidazolium chloride, present a more manageable profile from both an environmental and operational safety standpoint. Unlike salts containing more hazardous anions or volatile organic solvents, this compound generates a smaller hazard footprint in our workflows. Emergency drills, waste tank cleanouts, and accidental spill responses proceed with less worry since the compound lacks nerve-wracking byproducts.

    For handling, we insist on storing all drums only in dry, cool areas, as even moderate humidity spikes will nudge the water content higher over time. Staff wear standard lab safety gear, routinely check seals on drums, and treat the material with respect—though the risk profile is far more contained than comparable alternatives. We work with waste managers and compliance teams to ensure that end-of-life product finds its way to responsible disposal, and many customers select this compound partly due to easier downstream cleanup than fluorinated or phosphonate salts.

    Continuous Learning and Open Communication with End-Users

    We pride ourselves on maintaining active dialogue with our customers. Their feedback refines our production, and our troubleshooting on their real-world reactions informs the next round of quality improvements. Speaking directly to end-users—not just lab managers or buyers—has shaped our approach, from batch scale-up to the detail included in each certificate of analysis. Every comment, question, or flag raised during product trials feeds into our decision-making and often results in faster identification of new applications or performance needs.

    Sometimes, researchers push the limits of our standard product, demanding higher concentrations, purer runs, or novel blends. These challenges keep our team focused and humble. By including them early and often in our development cycle, we ensure the next generation of the carboxyethyl-3-methylimidazolium chloride fits the evolving needs of both science and production.

    Final Thoughts: Quality through Experience

    Every kilogram of 1-carboxyethyl-3-methylimidazolium chloride leaving our plant carries with it the checks, double-checks, and lessons learned across dozens of batches and years of daily production. Our methods grew from practical trial and error, not from copying textbook procedures. By sticking close to our core values—closely monitored synthesis, open communication, clear testing, and a willingness to adapt—we’ve managed to deliver a product that meets the rising bar in advanced ionic liquid applications.

    The performance, safety, and convenience offered by our refined carboxyethyl-methylimidazolium chloride stem directly from the long feedback loop between our plant floor and your laboratory or pilot plant. Each batch tells a story—one of avoided setbacks, founded improvements, and tangible benefits to researchers and production teams alike. This commitment drives us to keep listening, keep improving, and always back up every shipment with both expertise and full transparency.