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1-Carboxymethyl-3-Methylimidazolium Chloride

    • Product Name 1-Carboxymethyl-3-Methylimidazolium Chloride
    • Alias CMIM-Cl
    • Einecs 613-414-7
    • 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
    VTB
    Specifications

    HS Code

    998303

    Product Name 1-Carboxymethyl-3-Methylimidazolium Chloride
    Cas Number 870718-29-3
    Molecular Formula C7H11ClN2O2
    Molecular Weight 190.63 g/mol
    Appearance White to off-white solid
    Melting Point Approximately 92-95 °C
    Solubility In Water Highly soluble
    Density 1.26 g/cm³ (approximate)
    Boiling Point Decomposes before boiling
    Iupac Name 1-(Carboxymethyl)-3-methyl-1H-imidazol-3-ium chloride
    Smiles CC1=CN=CN1CC(=O)O.Cl
    Storage Conditions Store at room temperature, tightly closed
    Hazard Statements Irritant to eyes and skin

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

    Packing & Storage
    Packing 100g of 1-Carboxymethyl-3-Methylimidazolium Chloride is supplied in a tightly sealed, amber glass bottle with clear hazard labeling.
    Shipping **Shipping Description:** 1-Carboxymethyl-3-methylimidazolium chloride is shipped in tightly sealed containers, protected from moisture and direct sunlight. Classified as a chemical reagent, it should be handled with appropriate safety measures and shipped according to local, national, and international regulations for non-hazardous chemicals. Avoid sources of ignition and incompatible substances during transport.
    Storage 1-Carboxymethyl-3-methylimidazolium chloride should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area. Protect it from moisture, direct sunlight, and sources of ignition. Store away from incompatible substances such as strong oxidizing agents. Ensure containers are clearly labeled, and handle under conditions that prevent contamination and degradation. Use appropriate personal protective equipment when handling.
    Application of 1-Carboxymethyl-3-Methylimidazolium Chloride

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

    1-Carboxymethyl-3-methylimidazolium chloride is a functional ionic liquid ingredient that downstream industries employ for specialized process improvements, solubilization, and catalysis. As an experienced manufacturer, we support diverse sectors with consistent quality material that meets stringent manufacturing and regulatory benchmarks. Below are main application scenarios that leverage its unique chemical profile for commercial-scale production.

    1. Cellulose Dissolution for Fiber and Film Production

    Leading viscose and technical cellulose manufacturers use this ionic liquid in direct dissolution processes to achieve uniform polymer solutions, enabling continuous processing of textile fibers, regenerated films, and specialty membranes. It replaces conventional solvents in closed-loop systems, reducing environmental impact while allowing controlled polymer chain modification essential for advanced end-product quality. Careful adjustment of the ingredient loading ensures solution stability and viscosity suitable for extrusion or casting lines, integrating seamlessly into modern fiber spinning and film regeneration units.

    Industry compliance standards

    • OEKO-TEX® STANDARD 100, Annex 6: Limit values for harmful residues in textile production
    • ISO 9001:2015 – Quality management for chemical processing
    • OECD Test Guidelines for ready biodegradability (301 series)
    • ZDHC MRSL (Manufacturing Restricted Substances List)

    Typical usage ratio

    • 28–35% by weight of total solvent system, adjusted based on cellulose degree of polymerization and desired dope concentration

    Downstream process integration

    • Charged into first-stage dissolvers alongside alkaline co-solvents and cellulose source; maintained under temperature-controlled agitation before being filtered and processed through spinnerets or casting heads

    Final product types

    • Lyocell fibers (textile and technical grades)
    • Cellulosic films for packaging (biodegradable wrappers, food film)
    • Hemicellulose membranes (ultrafiltration and nanofiltration media)

    2. Electrolyte Formulation in Lithium-Ion Battery Manufacturing

    Battery manufacturers employ this imidazolium-based ionic liquid as a key functional additive in high-performance electrolyte blends, particularly for high-voltage or flame-retardant lithium-ion cell systems. Its ionic conductivity, electrochemical stability, and low volatility enable safer, long-lasting cells with widened temperature windows. Downstream cell assembly lines dose this ingredient precisely to enhance cycle stability and shelf-life without compromising separator or anode interfaces.

    Industry compliance standards

    • IEC 62660-2:2018 – Safety requirements for lithium-ion batteries for vehicles
    • UN Manual of Tests and Criteria, Part III, subsection 38.3 (Battery transport safety)
    • ISO 14001:2015 (Environmental management systems for battery production)
    • RoHS Directive (Restriction of Hazardous Substances in electrical/electronic equipment)

    Typical usage ratio

    • 5–12% by weight of total electrolyte blend, adjusted relative to desired ionic conductivity and voltage requirements

    Downstream process integration

    • Introduced in controlled dry-room environments during electrolyte mixing, after base solvents and lithium salts; thoroughly mixed with agitation before subsequent cell filling under inert atmosphere

    Final product types

    • Prismatic and cylindrical lithium-ion cells for power tools and e-mobility
    • Solid-state battery modules
    • High-safety batteries for grid storage and wearable electronics

    3. Homogeneous Catalysis for Esterification and Transesterification

    Chemical processors leverage this compound as a phase-transfer catalyst and ionic medium in the synthesis of esters from fatty acids and alcohols, including complex polyol esters for lubricants and specialty surfactants. Its high ionic strength and thermal stability facilitate single-phase reactions, enabling faster kinetics and easier post-reaction separation. This additive often appears in continuous-flow reactor setups, supporting precise process control for high-purity ester production in compliance with demanding performance standards.

    Industry compliance standards

    • ISO 21469:2006 – Safety in the manufacture of lubricants for incidental food contact
    • REACH Regulation (EC 1907/2006)
    • EU Regulation No 10/2011 on food contact materials where applicable
    • Good Manufacturing Practice (GMP) guidelines for chemical plants

    Typical usage ratio

    • 0.5–3% by weight of the total reactants; adjustment depends on reactant chain length and polarity

    Downstream process integration

    • Dosed into jacketed batch or flow reactors at initial charge phase, maintained at reaction setpoint throughout; removed via phase separation post-synthesis, usually recycled with solvent recovery systems

    Final product types

    • High-purity synthetic esters (lubricants, plasticizers)
    • Nonionic surfactant bases
    • Tailored functional fluids (refrigerant oils, transformer fluids)

    4. Biomass Pretreatment for Second-Generation Biofuels

    Biofuel producers apply this ionic liquid in lignocellulosic biomass pretreatment operations to disrupt cellulose–lignin networks without degrading fermentable sugars. This step increases downstream enzymatic accessibility and conversion rate for advanced bioethanol or biochemical routes. Closed-loop recovery methods limit solvent losses and support sustainable process cycles meeting modern biofeedstock guidelines. Dosing strategies reflect biomass heterogeneity and plant throughput capacities, integrated as an early stage prior to enzymatic hydrolysis and fermentation.

    Industry compliance standards

    • ISCC EU Certification (sustainability and GHG savings)
    • EPA Renewable Fuel Standard (RFS2) for eligible feedstocks
    • EN 16709:2015 (sustainability of biomass for energy applications)
    • ISO 22000:2018 – Where food-grade ethanol is the final product

    Typical usage ratio

    • 15–30% by weight relative to the dry biomass charge, with actual loading tailored to lignin content of feedstock and required pretreatment severity

    Downstream process integration

    • Pulped with biomass in high-shear, heated mixers prior to dilution and enzyme addition; recycled in solvent recovery systems for repeated cycles

    Final product types

    • Second-generation bioethanol (fuel grade)
    • Biobutanol and cellulosic-derived biochemicals
    • Lignin-rich residues for energy or material use

    5. Green Solvent for Pharmaceutical API Synthesis

    API manufacturers select this ionic liquid as a green reaction solvent for peptide and heterocyclic compound synthesis. Its low vapor pressure, inertness to common functional groups, and ability to stabilize reactive intermediates allow tight control over step yields, chiral purity, and product isolation. Compliance with process safety and extractable profiles is continually evaluated through QC and regulatory audits. Inclusion rates reflect process mass intensity, product solubility, and downstream isolation techniques like crystallization or extraction.

    Industry compliance standards

    • ICH Q7: Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP-NF (United States Pharmacopeia–National Formulary) standards for solvent residues
    • 21 CFR Part 211 (FDA cGMP for finished pharmaceuticals)
    • EU EudraLex Volume 4 (GMP for pharmaceutical production)

    Typical usage ratio

    • 10–25% by weight of total reaction mass, modulated by solubility of reactants and target purity requirements

    Downstream process integration

    • Added at initial stage of API reaction setup in cleanroom-grade reactors; removed at workup through aqueous extraction or distillation with validated recovery rates

    Final product types

    • Active pharmaceutical ingredient (API) intermediates
    • Peptide drugs
    • Specialty pharmaceutical compounds requiring high-purity syntheses

    6. Additive for Anti-Static Polymer Compounding

    Manufacturers of conductive and anti-static polymer grades use this compound as a highly effective ionic charge carrier in polyolefin or engineering thermoplastic masterbatches. Incorporated during melt compounding, it imparts surface resistivity control while preserving mechanical properties and compliance with electrical goods or packaging safety requirements. Typical dosages are selected to meet end-user performance targets and are validated in test moulding and extrusion runs for uniform dispersion and shelf stability.

    Industry compliance standards

    • UL 94 (flammability of polymeric materials)
    • IEC 61340-5-1: Electrostatic discharge (ESD) protection
    • FDA 21 CFR 177.1520 for polyolefin contact materials (where required)
    • REACH Regulation for polymer additives

    Typical usage ratio

    • 0.3–1.2% by weight of compound, tuned to target surface resistivity class and host resin compatibility

    Downstream process integration

    • Dry blended with base polymer resin and other additives prior to extrusion or injection compounding; processed under standard melt temperatures to ensure molecular-level distribution

    Final product types

    • Anti-static films and sheets
    • Conductive packaging for electronics
    • ESD-safe automotive and consumer device parts
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    Certification & Compliance
    More Introduction

    Unpacking 1-Carboxymethyl-3-Methylimidazolium Chloride: A Manufacturer’s Perspective

    What Goes Into Every Batch

    Every batch of 1-Carboxymethyl-3-Methylimidazolium Chloride we produce brings together precision, purpose, and refinement. This isn’t a random compound off a catalog page. Years of hands-on process improvement, rigorous purification steps, and keen quality observation shape each lot. Tight control on inputs and exact handling of reagents like methylimidazole and chloroacetic acid create consistency in structure and purity, which customers downstream recognize when they handle our material.

    We never treat this salt as just another ionic liquid derivative. From the early mornings of initial synthesis to the late-day checks in our quality control labs, we aim for the right physical and chemical profile: white crystalline powder, stable under ambient conditions, and packing a strong hydrophilic character from the carboxymethyl group. Every operator on the line knows what it means if the pH drifts or the product picks up even a trace of color – we trace the source, scrub the result, and make sure what leaves our facility meets the tight specs we’d demand ourselves.

    Model and Specifications We Stand By

    In chemical manufacturing, true pedigree doesn’t lie in price sheets or flashy brochures. We base our credibility on transparency and test results. For 1-Carboxymethyl-3-Methylimidazolium Chloride, that reputation builds on certified HPLC purity over 99%, water content routinely tested before and after drying, and batch documentation stretching back years.

    We package this chloride in multiple sizes, but the model that sees the most customer traffic has a particle size optimized for both solubility and handling. We control particle size distribution to keep dusting low in larger operations, but still fine enough to dissolve quickly in aqueous or polar organic media.

    Customers who have moved from alternative ionic liquids often note our product’s potassium and sodium levels, kept in check well below 200 ppm, and appreciate the absence of typical halide or amine byproducts. The chloride counterion, sourced from ultra-high-purity hydrochloric acid, helps assure reliable downstream reactivity. If you ever spill a gram on your glove, you find no persistent odor or tacky residue — detailed small touches only possible after repeated process tuning.

    Molecular Differences: Not Just a Name Change

    1-Carboxymethyl-3-Methylimidazolium Chloride might sound like chemistry alphabet soup at first read, but we have learned from trial and error just how significant the impact of these structural motifs can be. The carboxymethyl group, attached at the first position of the imidazolium ring, gives this molecule unique versatility. In contrast, the more commonplace 1,3-dimethylimidazolium salts lack that carboxylate handle, limiting their use in some fields.

    For chemists working in phase transfer catalysis or enzymatic reaction support, the presence of the carboxymethyl allows functionalization and binding options that other imidazolium salts simply cannot deliver. Peptide chemists and bioconjugate developers have reported greater results because the carboxymethyl encourages hydrogen bonding or acts as a reactive site for further modifications. We have watched academic and industrial partners build applications from protein stabilization to analytical extraction methods, all pivoting on this extra carboxylic acid group.

    Laboratory teams working with common chloride salts of imidazoliums know the tradeoffs: many similar compounds introduce unwanted ionic strength or sodium, yet lack the fine-tuned selectivity possible here. Our formulation, pumped through multiple ion-exchange columns and trace metal scavenging steps, keeps the matrix clean for sensitive catalysis, analytical standards, and even emerging green solvent uses.

    Why Chemists and Engineers Return to This Salt

    No compound solves every technical challenge, but the design of 1-Carboxymethyl-3-Methylimidazolium Chloride consistently catches the eye of chemists needing more than routine. We hear from formulation managers who want both ionic strength and a reliable site for immobilization. Enzyme engineers looking to stabilize delicate proteins or switch catalysis pathways rely on this chloride for its gentle yet constant ionic character. Research groups exploring ionic liquids often start with a less functionalized salt and discover the limitations – then move to our carboxymethyl product for broader options.

    In our production facility, we’ve spent years refining the labor, temperature, and timing for each batch. The end result: a product that crystalline under practical storage conditions, ships with no significant lumping after months on the shelf, and exhibits consistent melting and decomposition behaviors during thermal analysis. Lab managers who call with requirements for solvent selection, custom pH ranges, or “clean room”-ready batches trust we can (and will) deliver, because we see their demands reflected in our own QC checks and stress testing.

    From Lab Bench to Industrial Scale: The Realities of Application

    We’ve seen this material poured into reaction flasks and loaded by the drum in pharmaceutical plants. The transition from milligram to metric ton doesn’t happen overnight. Research partners, pilot plant managers, and purchasing officers scrutinize every variable, from solubility curves to residue levels after drying. In meetings with process engineers and application scientists, we hear plenty about bottlenecks – filtration, heat transfer, incomplete dissolution, and waste stream control. We have answered those challenges by continuous review and adaptation.

    Some clients arrive with new electrochemistry needs, others want an excipient that tolerates broad pH variation. Cosmetic manufacturers test our ionic liquid for stability with surfactants or proteins, reporting how our careful control of organic byproducts spares them from unexpected fogging or precipitation over time. Green chemistry developers ask us pointed questions about lifecycle impact and recoverability – with this carboxymethyl functionality, recycling protocols take on new ease, letting users precipitate or extract the ionic liquid with higher efficiency than standard dialkyl imidazoliums.

    Learning from Our Customers: Continuous Improvement

    Direct feedback from users shapes the way we approach the next batch. We encourage our clients to challenge us with real questions – does the chloride interfere with silver-catalyzed coupling? Can the carboxymethyl survive under strong base? Does scale-up to 500 kilograms bring out batch-to-batch drift? These aren’t academic questions. They’re hard facts that impact costing, rework, and time to market on the customer side, and we see them as a chance to show what happens when the manufacturer’s floor listens with both ears.

    Some issues land on our doorstep routinely: residual solvent levels, filtration speed, or thermal stability. We tackle these by modifying drying protocols or tweaking crystallization rates, testing each time with real-world protocols – not just textbook methods. When universities and corporations chose this product for new applications, they bring us into the experimental conversation, letting us tailor product lines to the specific quirks of their processes. It’s a back-and-forth that lifts the level for everyone, from our own operations crew to bench chemists around the world.

    Safe Handling and Long Shelf Life Require Diligence

    Any specialty chemical benefits from careful storage. 1-Carboxymethyl-3-Methylimidazolium Chloride doesn’t absorb moisture the way its acetate cousins might. Still, we always suggest airtight drums and low-light storage. Our facility packs each batch under dry nitrogen and cycles through inventories using strict rotation policies. This way, customers open bags with confidence, seeing a bright, creamy powder—never damp clumps or darkened crystals.

    Over the years, we’ve measured shelf life under a range of temperatures and humidities. Time after time, the product holds strong for over a year with negligible decomposition. The unique construction of the carboxymethyl group appears to offer extra stability compared to more basic imidazolium salts. Still, nothing replaces careful packaging: double-lined bags, outer drums, and real-time monitoring of warehouse climate.

    Solubility, Compatibility, and Routes to Green Processing

    Chemists get the most out of our material when they understand its unique solution behavior. This chloride salt brings better solubility in both water and polar organics than most alternative imidazolium-based products. The presence of the carboxyl group not only speeds up dissolution but also lets the compound interact with amino acids, proteins, and nucleic acids in ways regular methylimidazoliums cannot. Our own electrochemistry team found this an asset for developing new gel electrolytes and antifouling additives.

    With green chemistry in sharp focus, we see increased demand for recyclable and non-toxic ionic liquids. In several trials, users have reclaimed our product from aqueous streams by simple pH swings, with minimal side reactions. It means less material lost to waste and less effort spent dealing with residues downstream. The absence of persistent halide or conjugated amines means the product leaves less impact on sensitive fermentation or cell culture systems—a factor that makes a difference for the biotech sector.

    Reliability and Traceability in Every Sack

    All of us in this business have seen the headaches that come from batch drift or inconsistent raw material streams. We learned early on that even small fluctuations in chloride or trace heavy metal levels can damage reproducibility. Our process uses traceable, certified reagents, and every batch receives a digital birth certificate. That audit trail carries weight—not just for regulatory auditors, but for customers need to pinpoint a source for any future troubleshooting.

    Years of in-house development taught us that it’s better to invest upfront in raw material quality than to repair a reputation after a problem appears in the field. Our lab technicians retain reference samples from every batch for at least two years, and we welcome re-analysis orders or special documentation needs. This transparency cements long-term working relationships, especially with those running multicenter trials or regulatory submissions.

    Differences That Make the Product Work—Not Just Appear Unique

    It’s tempting to view new salts as little more than small tweaks on an old formula, but in practice, the carboxymethyl group has enabled applications that solidify its place in advanced synthesis. Other imidazolium salts, particularly straight alkyl derivatives, offer less versatility for bioconjugation or immobilization. Companies edge into new synthesis territory by using this salt as a stepping-stone toward surface modification, advanced catalysis, or media for biological transformations. The neutrality of the chloride ion, its relatively clean background in mass spectrometry or NMR, and its amicable dissolution properties all count when researchers want to conserve both time and raw material costs.

    Customers speak up about the difficulty purifying related chemicals after protein contact, noting stubborn residues that break down at undesirable points. The carboxymethyl variant’s added functional group helps sidestep those pitfalls. Those differences may not obviously jump from the material safety sheet, but for labs chasing higher margins or deeper reproducibility in their data, such advantages aren’t trivial. The number of repeat buyers we see reflects the kind of confidence built through performance rather than marketing speak.

    Looking Ahead: Thinking Beyond Commodity Chemistry

    1-Carboxymethyl-3-Methylimidazolium Chloride, in our hands, has become both a reliable staple and a springboard to innovation. We listen to the field and shape our operations to keep pace. In the next decade, fields like synthetic biology, electrochemistry, and advanced catalysis are only going to stretch the performance requirements further. We constantly explore scale-up routes that keep the quality of small batches while expanding to larger reactors, and we invest in analysis tools that catch issues before they leave the plant. Our R&D team fields suggestions straight from the end users, keeping everyone focused on tangible performance and practical improvements.

    Performance in the real world never comes down to purity percentages and theoretical values alone. It lives in the consistency of each sack delivered, the crisp responses to technical queries, and the willingness to fix the rare batch problem before it mushrooms. As manufacturers, we know the material’s real worth is proven by the hands of chemists, process operators, and analytical scientists using it every day. Our 1-Carboxymethyl-3-Methylimidazolium Chloride continues to expand boundaries, not by being new for the sake of novelty, but by solving stubborn problems and standing up to tough scrutiny batch after batch.