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1-(Methoxycarbonyl)Methyl-3-Methylimidazolium Chloride

    • Product Name 1-(Methoxycarbonyl)Methyl-3-Methylimidazolium Chloride
    • Alias MMIM-Cl
    • Einecs 674-110-6
    • 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

    538995

    Productname 1-(Methoxycarbonyl)Methyl-3-Methylimidazolium Chloride
    Casnumber 99606-03-0
    Molecularformula C8H13ClN2O2
    Molecularweight 204.66
    Appearance White to off-white solid
    Meltingpoint 125-130°C
    Solubility Soluble in water
    Purity Typically >97%
    Storagetemperature Store at 2-8°C
    Iupacname methyl 1-(3-methylimidazol-1-ium-1-yl)acetate chloride
    Synonyms MMAImCl, 3-Methyl-1-(methoxycarbonylmethyl)imidazolium chloride

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

    Packing & Storage
    Packing Sealed amber glass bottle labeled "1-(Methoxycarbonyl)methyl-3-methylimidazolium chloride, 25g," with hazard symbols, lot number, and storage instructions.
    Shipping 1-(Methoxycarbonyl)methyl-3-methylimidazolium chloride is shipped in tightly sealed containers under ambient conditions. Packaging ensures protection from moisture and contamination. Handle with appropriate personal protective equipment. Complies with all chemical shipping regulations. Not classified as hazardous for transport; however, care should be taken to avoid spills and direct contact during transit.
    Storage Store 1-(Methoxycarbonyl)methyl-3-methylimidazolium chloride in a cool, dry, and well-ventilated area, away from heat sources, moisture, and incompatible substances such as strong oxidizers. Keep the container tightly closed and clearly labeled. Protect from direct sunlight. Use appropriate personal protective equipment when handling. Follow all relevant safety data sheet (SDS) recommendations for storage conditions and handling procedures.
    Application of 1-(Methoxycarbonyl)Methyl-3-Methylimidazolium Chloride

    Applications of 1-(Methoxycarbonyl)Methyl-3-Methylimidazolium Chloride in Industrial Manufacturing

    As a direct manufacturer, we supply 1-(Methoxycarbonyl)Methyl-3-Methylimidazolium Chloride for several advanced industrial uses. Our industrial partners apply this ionic liquid in specialty synthesis, catalysis, and ESD-control polymer manufacturing, with high requirements for process adaptability, purity, and conformity. We ensure each customer receives consistent technical support aligned with real-world production demands.

    1. Catalytic Medium in Pharmaceutical Intermediate Synthesis

    Pharmaceutical manufacturers use this imidazolium-based ionic liquid as a solvent and co-catalyst in select alkylation, esterification, and condensation steps for APIs and high-value intermediates. Its low volatility, high ionic conductivity, and specific reactivity profiles enable lower reaction temperatures and increased selectivity in certain pyridine, benzofuran, or heterocycle syntheses. Scale-up often requires comprehensive HSE evaluation, solvent recycling, and purity audits to satisfy regulatory inspections and batch reproducibility targets.

    Industry compliance standards

    • ICH Q7 (Good Manufacturing Practice for Active Pharmaceutical Ingredients)
    • 21 CFR Part 210/211 (US FDA Drug GMP regulations)
    • EU EudraLex Volume 4 (EU GMP Guide for medicinal products)
    • Chinese Pharmacopoeia (ChP) standards for drug synthesis solvents

    Typical usage ratio

    • 5-20% by weight in reaction media, adjusted according to substrate loading and targeted yield; process development determines the final ratio to balance selectivity and extraction efficiency.

    Downstream process integration

    • Charge after initial raw material blending and before temperature ramping in batch reactors.
    • Solvent recovery and in-line purification occur post-reaction to minimize residue in API output.

    Final product types

    • Pyridine-based intermediates
    • Active pharmaceutical ingredients for cardiovascular or antiulcer drugs
    • Benzofuran API precursors
    • Custom fine chemical medicinal building blocks

    2. Electrolyte Additive for Battery and Supercapacitor Manufacturing

    Energy storage manufacturers select this material for its high thermal stability and ionic conductivity performance in next-generation lithium-ion battery and hybrid supercapacitor electrolytes. It supports the safe design of advanced electrolytes that must function under high-voltage or extended storage conditions, where traditional organic solvents fail. Our on-site quality control confirms trace impurity limits and water content directly support downstream electrode coating and assembly process requirements for Asian, European, and American gigafactory customers.

    Industry compliance standards

    • UN 38.3 (Battery Transport and Safety Testing)
    • IEC 62133-2:2017 (Safety requirements for portable sealed batteries)
    • REACH Regulation (EC) No 1907/2006 for electrolyte components
    • UL 2054 (Household and Commercial Batteries)

    Typical usage ratio

    • 1-10% additive in overall electrolyte formula; proportion tuned for targeted ion transport and viscosity optimization, typically through pilot cell cycling tests.

    Downstream process integration

    • Added during main electrolyte mixing before electrode wetting.
    • Subjected to vacuum drying and physical stability checks to meet target water content (<20 ppm).

    Final product types

    • Rechargeable lithium-ion battery cells
    • Hybrid electrochemical supercapacitors
    • Grid-level backup storage modules
    • Consumer electronics battery packs

    3. Antistatic Additive in Specialty Polymer Production

    High-end plastics processors introduce this ionic liquid as a permanent internal antistatic additive in technical polymers such as polyamides and polycarbonates, where electronic circuitry and medical device casings demand strict ESD (Electrostatic Discharge) management. Its permanent ionic mobility prevents static buildup during injection molding and extended service, without sacrificing transparency, mechanical integrity, or biocompatibility of the base polymer. Our continuous supply ensures lot-to-lot consistency for critical process controls and final QA release.

    Industry compliance standards

    • EN 61340 (Electrostatics – ESD protective materials)
    • RoHS Directive (2011/65/EU) for electrical safety and restricted substances
    • FDA 21 CFR 177.1500 (Polymers for food contact, if used in relevant products)
    • UL 94 and IEC 60695 (Flammability for plastics)

    Typical usage ratio

    • 0.2–1.5% by polymer weight; precise concentration adjusted according to surface resistivity targets and downstream mechanical test results.

    Downstream process integration

    • Dry-blended into polymer pellets or compounded via twin-screw extrusion prior to molding operations.
    • Material integrity validated by in-process surface resistance and haze measurements.

    Final product types

    • Antistatic device housings
    • Medical electronic casings
    • Precision injection-molded ESD-sensitive tools
    • Transparent polymer films for cleanroom packaging

    4. Solvent for Homogeneous Catalysis in Fine Chemical Manufacturing

    Fine chemical companies deploy this ionic liquid as a green, recyclable reaction medium for homogeneous metal-catalyzed processes, including selective hydrogenation and C–C coupling reactions. The compound's negligible vapor pressure, strong coordination properties, and compatibility with transition metal complexes allow process engineers to achieve higher turnover numbers and efficient product separation. Residual solvent analysis, spent catalyst separation, and integrated solvent recovery represent critical elements of our technical support.

    Industry compliance standards

    • Responsible Care Global Charter for sustainability and environmental control
    • OECD Good Laboratory Practice (GLP) principles for specialty chemicals
    • ISO 9001:2015 (Quality management for chemical synthesis)
    • Local Environmental Emission Regulations (for solvent recovery efficiency)

    Typical usage ratio

    • 15–40% by total reaction mass; ratio tuned according to substrate solubility and targeted product partitioning, typically confirmed by per-batch process validation.

    Downstream process integration

    • Buffered addition into jacketed batch reactors after catalyst charging.
    • Product extraction and solvent recycling steps follow reactive phase completion, enabling closed-loop operation.

    Final product types

    • Specialty alcohols and amines
    • Biphenyl and aromatic intermediates
    • Custom-organic catalysts for pharmaceutical and agrochemical use
    • Chemical intermediates for flavors and fragrances
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    Certification & Compliance
    More Introduction

    Introducing 1-(Methoxycarbonyl)Methyl-3-Methylimidazolium Chloride: Precision for Advanced Chemical Synthesis

    Direct from the Manufacturer: Experience and Commitment in Every Batch

    Our history with imidazolium-based chemicals goes back more than a decade. In that time, we have seen the demand for specialized ionic liquids increase rapidly. Research laboratories, pharmaceutical developers, and industrial chemists all look for finer purity, tighter batch consistency, and greater reliability from their suppliers. From our earliest days, we invested in dedicated production lines for imidazolium salts, and over time, 1-(Methoxycarbonyl)Methyl-3-Methylimidazolium Chloride has become one of our flagship offerings. Its combination of molecular structure, functional groups, and chloride counterion offers versatility for both established and novel transformations.

    1-(Methoxycarbonyl)Methyl-3-Methylimidazolium Chloride stands out as a functional task-specific ionic liquid. Some projects require more than just a solvent or generic imidazolium salt. This product, which we abbreviate as [MMCIM][Cl], features a methoxycarbonyl group attached via a methyl linker to the imidazolium nitrogen. That distinction may sound technical, but to synthetic chemists and formulation teams, this detail changes the way the molecule interacts in solution, influences reactivity, and governs its compatibility with a range of substrates. Our process uses controlled temperature profiles and high-purity starting materials, avoiding contamination from common side products that disrupt either assay readouts or downstream processing.

    Specifications That Reflect Real-World Demands

    We manufacture 1-(Methoxycarbonyl)Methyl-3-Methylimidazolium Chloride in batches ranging from pilot-plant scale up to multi-hundred-kilogram lots. Our typical assay runs well above 98% by HPLC, thanks to a combination of careful distillation, careful washing protocols, and real-time inline monitoring during synthesis. The final powder is highly hygroscopic, which means the packaging and handling demand extra attention. We use moisture-barrier laminated pouches inside high-density polyethylene drums—solutions that came directly from feedback by lab managers and logistics coordinators who experienced clumping and hydrolysis with lesser grades from other sources.

    The chloride counterion provides a distinct set of benefits over tetrafluoroborate or hexafluorophosphate analogs. We have worked with several academic and commercial partners who require chloride because it easily participates in nucleophilic substitution, or helps control ionic balance during metathesis and phase-transfer processes. For reactions in aqueous solutions, chloride ions stay highly soluble and avoid precipitation with standard cations such as sodium or potassium. That keeps vessel cleaning less laborious and cuts down on waste streams; operators have commented on this improvement more than once since we upgraded our purification methods several years ago.

    Why Structural Variations Matter

    Years of hands-on production have taught us that even minor changes in side-chain composition lead to major differences in chemical behavior. Substituting the methoxycarbonyl unit for an alkyl or sulfonate group, or swapping methyl for ethyl, alters polarity, hydrogen-bonding, and thermal stability. Our customers’ results in catalysis, electrochemistry, and green extraction processes highlight this fact. During recent process optimizations, a pharmaceutical customer exploiting [MMCIM][Cl] as a phase-transfer catalyst found dramatic increases in both product recovery and selectivity when compared against standard 1-butyl-3-methylimidazolium chloride. They attributed this, in their own published research, to the electron-withdrawing strength of the methoxycarbonyl substituent and its effect on cation-anion interactions.

    We have provided technical guidance on solvent-media optimization for advanced glycosylation protocols, where yield hinges on fine-tuning the ionic environment. More than one industrial partner has validated that switching from classic imidazolium salts to our methoxycarbonyl-functionalized model enabled translation of research-level batch syntheses to reliable, GMP-compliant pilot runs. Reproducibility is not a slogan here — purity audit trails and batch-to-batch chromatogram overlays are available for every lot, so development teams do not waste time questioning their raw materials.

    Applications: Where 1-(Methoxycarbonyl)Methyl-3-Methylimidazolium Chloride Shows Its Value

    Chloride-imidazolium salts with functionalized side chains are not generic commodities, and it only takes a poorly performing batch from another producer to make this clear. In alkylation catalysis, [MMCIM][Cl] can minimize side reactions by providing a less nucleophilic and more selective reaction medium. This property becomes critical in pharmaceutical intermediate synthesis, where complex, multi-step transformations happen in a confined space. One of our early customers in the custom synthesis sector commented that what drew them to this product was a consistent reduction in methylation byproducts during the preparation of sensitive carbamoyl intermediates.

    Electrochemical energy storage is a newer field benefitting from imidazolium-based liquids. We have been involved in several collaborations aiming to develop more stable electrolytes for advanced batteries. The unique cation-anion pair in [MMCIM][Cl] delivers both a high ionic conductivity and a wide electrochemical window. This keeps performance stable during repeated charging cycles and resists degradation much better than unsubstituted imidazolium chlorides. Thanks to these properties, several research groups have requested custom scaled batches for pre-commercial pilot cells, and we have worked directly with their engineers to adjust drying protocols and packaging for glovebox compatibility.

    Extraction and separation science has also opened new application streams. Chemists developing “green chemistry” solutions find that [MMCIM][Cl] gives them the right balance of miscibility, extracting power, and selective solvation when moving to biobased or waste-derived starting materials. A leading food analysis laboratory reported higher recovery of certain vitamin esters versus more hydrophobic or less functionalized imidazolium salts, which they correlated to the polarity introduced by the methoxycarbonyl group. Our in-house R&D team followed up on these field reports, adapting and refining our purification steps to increase product stability in open-atmosphere protocols.

    Comparison and Distinction from Other Products

    The ionic liquid market now includes a broad range of imidazolium, pyridinium, and phosphonium salts. Generic 1-butyl-3-methylimidazolium chloride (BMIM Cl) dominates the lower-cost segments, suited for simple dissolving or ion-exchange applications. Yet in our experience, process chemists notice substantial differences as soon as product requirements move beyond basic solubility. Our [MMCIM][Cl] consistently delivers tighter NMR spectra, lower levels of trace halide contamination, and less thermal decomposition under elevated-temperature protocols compared with either BMIM Cl or 1-ethyl-3-methylimidazolium chloride (EMIM Cl).

    Other suppliers sometimes substitute related methylcarbonate or methyl ester analogs and present these as interchangeable. Our project reviews with downstream users have proven otherwise. The introduction of the methoxycarbonyl methyl group modulates hydrophilicity; that translates into lower toxicity and reduced volatility, two parameters that become important during scale-up or in continuous-flow systems. One large-scale agricultural chemistry developer specified [MMCIM][Cl] exclusively for a series of process development trials after alternate materials led to unexpected emulsion and salt precipitation issues. Their shift to our product reduced their maintenance intervals and improved batch homogeneity, based on direct process measurements.

    At the packaging and storage stage, we have heard complaints about caking and slow dissolution with lower-grade products from buyers repackaging bulk material from overseas brokers. By controlling particle size during drying and maintaining strict humidity controls up to final shipment, we have minimized both issues. Customer labs noticed the difference right away — faster dissolution means quicker setup, shorter downtime, and fewer vessel residues. That feedback cycle drives our internal process improvements and influences every procedure update, from synthesis up to the final QA release.

    The Human Side of Production: Lessons from Hands-On Manufacturing

    Our team of production chemists and quality engineers has worked through numerous challenges, and each batch reflects the lessons learned in the real workplace, not just in theory or controlled pilot trials. For example, strict avoidance of metal catalysis contamination has led us to rely on glass-lined reactors and proprietary filtration systems. That choice stemmed directly from user requests for products unaffected by heavy-metal traces, particularly for those operating under high regulatory scrutiny in pharmaceutical development or advanced materials R&D.

    We maintain full chain-of-custody control. Real audit data, not marketing promises, support every certificate of analysis we issue. Years ago, we learned that a single unexplained impurity spike late in production could delay a customer’s next batch, waste valuable time, and compromise an entire drug synthesis campaign. This awareness shapes our daily operations, from linking process analytics to floor operators’ workflow all the way to logistics and batch tracking. Delivering every shipment with the expected analytical profile is a daily practice, not a slogan. If something reaches out-of-spec, our technical staff responds—not a distant call center or third-party distributor. That is the only way we have earned repeat business in such a competitive segment.

    The feedback footprint our chemists receive every year covers an impressive range of industries. Sizable pharmaceutical and agrochemical firms, new-energy startups, academic groups, and specialty food analysis labs all use our [MMCIM][Cl] in different ways. They count on that single product to perform, batch after batch, whether their goal is to run a lab-scale reaction for a new process route or to expand production for market launch. We have responded by making the tracking, fulfillment, and technical support systems as robust as the chemistry itself.

    Continuous Learning and Evolving Needs

    Technology advances constantly. Processes established five years ago are regularly replaced as regulatory demands change and new environmental standards tighten. We keep in close touch with the scientific literature and maintain an open line with industry R&D groups, so we can anticipate the next set of requirements. For instance, as attention toward high-recyclability ionic liquids grows, we have begun supporting customers with reuse and recovery studies specifically for [MMCIM][Cl]. Working together, we have established protocols for solvent recycling, downstream separation, and final purification to help extend raw material lifespans and reduce overall environmental impact.

    The new wave of “green” processes depends on materials that bring more than inert behavior—they need to reduce total process energy, cut emissions, and leave no harmful residue in finished goods. One project with a renewable fuel developer used our [MMCIM][Cl] as a catalyst-supporting medium, reporting energy savings based on its stability and high selectivity. We are convinced that the next generation of imidazolium-based chemicals will anchor vital sustainable transformations at both laboratory and industrial scale. That conviction comes not from trending keywords, but straight from data and real-world field reports sent in by hands-on users.

    Supporting Scientific Discovery and Industrial Growth

    Our philosophy treats every batch as the result of team expertise, technical rigor, and honest communication. We willingly provide full analytical packages, from NMR and elemental analysis through to residual solvent testing, because we know every parameter might influence a customer’s yield, safety profile, or regulatory stance. In turn, these customers inform us about their results, allowing us to refine internal standards and stay several steps ahead of market expectations.

    Researchers and production teams alike often prefer [MMCIM][Cl] for applications demanding specific structural or reactivity profiles. Its methoxycarbonyl side chain ensures selectivity or solubility advantages in several contemporary reaction systems. Even as new ionic liquids enter the market, we find that experience with day-to-day production and troubleshooting is valued above claims of theoretical performance.

    Every success story—whether a cleaner glycosylation, a more stable battery material, or a simpler cleanup after phase-transfer catalysis—builds on the foundation of reliability, transparency, and responsiveness. Our investments in analytical facilities did not happen overnight; they reflect lessons learned over years of putting our own product into critical supply chains and seeing where the bottlenecks and unknowns really occur. That on-the-ground learning is present in every kilogram delivered, ensuring that 1-(Methoxycarbonyl)Methyl-3-Methylimidazolium Chloride meets both textbook requirements and the more demanding realities of modern chemistry.

    An Invitation to Challenge and Collaborate

    Technical progress cannot be static, and our approach with 1-(Methoxycarbonyl)Methyl-3-Methylimidazolium Chloride stays rooted in dialogue with its users. By working with real feedback, tough application problems, and large-scale commercial projects, we keep evolving both the material and the technical solutions that go with it. Whether launching a new process, trouble-shooting a fail-point in production chemistry, or exploring the next sustainable synthesis platform, every batch we ship embodies not just the chemistry, but the lived experience of responding to real-world challenges.

    For teams ready to set new performance benchmarks in synthetic, analytical, or process chemistry, [MMCIM][Cl] offers a track record built on substance, not slogans. Our direct manufacturing background, transparent internal standards, and willingness to adjust for specific workflows mark the difference between a routine supply and a long-term technical partnership.