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HS Code |
311736 |
| Product Name | 1-(Ethoxycarbonyl)Methyl-3-Methylimidazolium Chloride |
| Cas Number | 824295-06-7 |
| Molecular Formula | C8H13ClN2O2 |
| Molecular Weight | 204.66 g/mol |
| Appearance | White to off-white solid |
| Purity | >98% |
| Solubility | Soluble in water |
| Storage Temperature | Store at room temperature |
| Synonyms | EMIM-Cl, 1-ethyl-3-methylimidazolium chloride |
| Hazard Statements | May cause respiratory irritation |
| Chemical Class | Imidazolium-based ionic liquid |
| Boiling Point | Decomposes before boiling |
As an accredited 1-(Ethoxycarbonyl)Methyl-3-Methylimidazolium Chloride factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 250g of 1-(Ethoxycarbonyl)methyl-3-methylimidazolium chloride, supplied in a sealed amber glass bottle with tamper-evident cap, labeled for laboratory use. |
| Shipping | 1-(Ethoxycarbonyl)methyl-3-methylimidazolium chloride is securely packaged in sealed containers to prevent moisture absorption and contamination. Shipped in compliance with relevant chemical transport regulations, it is labeled appropriately for safe handling. Temperature and humidity control may be implemented depending on quantity and destination, ensuring product integrity during transit. |
| Storage | 1-(Ethoxycarbonyl)methyl-3-methylimidazolium chloride should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from moisture and incompatible substances such as strong oxidizers. Protect from direct sunlight and sources of ignition. It is recommended to store the chemical at room temperature and ensure proper labeling and access control to prevent unauthorized handling. |
Applications of 1-(Ethoxycarbonyl)Methyl-3-Methylimidazolium Chloride in Industrial ManufacturingAs an experienced manufacturer of 1-(Ethoxycarbonyl)Methyl-3-Methylimidazolium Chloride, we supply this advanced ionic liquid to industrial partners who require precise formulation, excellent stability, and reliable integration into regulated manufacturing channels. Below are the principal application areas, with detail on compliance, dosage, integration points, and resulting finished industrial products. 1. Pharmaceutical Intermediate SynthesisPharmaceutical manufacturers use this chloride-based ionic liquid as a functional solvent and reaction medium during the synthesis of various active pharmaceutical ingredient (API) intermediates. The ionic character of the compound supports nucleophilic substitution and coupling reactions, often replacing less sustainable organic solvents. During scale-up, process engineers validate the raw material input in reaction vessels to achieve selective transformation of heterocyclic core structures. Traceability and full batch control ensure that the process meets stringent purity standards set by pharmaceutical authorities. Industry compliance standards
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2. Engineered Polymer ModificationAdvanced materials manufacturers select this imidazolium chloride for incorporation into polymerization processes to adjust polymer chain structure, enable ionic conductive properties, and support in-situ modification of engineering plastics. The compound assists with direct imidazolium functionalization on polymer backbones (e.g., application in poly(arylene ether) membranes or functionalized polyimides), achieving desired physical and electrical characteristics for electronics or specialty film production. Industry compliance standards
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3. Electrochemical Device ElectrolytesProducers of advanced electrochemical systems formulate with this compound to create ionic liquid-based electrolytes for supercapacitors, dual-carbon batteries, and next-generation electrolysis cells. The chloride anion and alkylimidazolium cation enable low volatility and high conductivity in non-aqueous systems. Mixing with other organic or inorganic salts creates tunable ionic conductivity profiles, which engineers characterize and adjust ahead of full-scale device assembly. Industry compliance standards
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4. Homogeneous Catalysis and Metal ExtractionSpecialty chemical processors utilize this imidazolium ionic liquid as a phase-transfer agent and reaction media for transition metal catalysis, including palladium- and copper-catalyzed coupling reactions. Hydrometallurgical operations employ it for selective metal ion extraction, particularly in recycling schemes for base and precious metals. The chloride ion facilitates solvation and extraction of metal complexes, improving yield and selectivity compared to traditional solvents. Plant managers tightly control batch addition and ensure compatibility with downstream purification processes. Industry compliance standards
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5. CO2 Capture and Separation MediaGas treatment plants and research-driven environmental facilities choose this chloride ionic liquid for integration as a CO2-selective absorbent during flue gas scrubbing and specialty gas purification. The unique solvation environment supports reversible CO2 absorption, facilitating more energy-efficient regeneration than amine-based systems. Operators carefully monitor loading and regeneration steps to prevent degradation and ensure consistent separation performance across long-duration cycles. Industry compliance standards
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6. Specialty Organic Synthesis and Research ReagentsContract research organizations (CROs) and fine chemical producers deploy this compound as a highly functionalized ionic liquid in tailor-made organic reactions, ultra-low temperature processing, and catalysis discovery projects. Its chemical structure offers unique solvation and phase properties sought after in emerging applications, such as organocatalysis and non-aqueous enzymatic chemistry. Researchers utilize it in gram-scale screens and expand to pilot-line runs as part of custom synthesis campaigns. Industry compliance standards
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Producing 1-(Ethoxycarbonyl)Methyl-3-Methylimidazolium Chloride begins at the reactor where we see every raw input combine under carefully controlled temperature and stirring. As chemical manufacturers, we monitor the whole synthesis, always focusing on quality, safety, and stability, because we know researchers and manufacturers count on a consistent product that behaves as expected, whether in the lab or at commercial scale. Over years of making specialty imidazolium salts, we have learned the significance of keeping every batch clean, reproducible, and free from trace contaminants. Experienced chemists notice quickly when off-standard lots creep into the chain, so hands-on quality checkpoints are set after each purification and drying step.
Our customers often ask: what sets this particular imidazolium salt apart from more familiar analogs? The answer sits in the unique combination of the ethoxycarbonyl-methyl group at the 1-position and the methyl group at the 3-position, each adding its own influence to the cation. The chloride anion brings a level of solubility and reactivity different from traditional non-coordinating anions such as PF6 or BF4. In the plant, these differences become clear in handling and post-synthesis workup. This compound flows well after drying and maintains stability in well-sealed, light-blocking packaging. Long-term shelf life depends on the environment, so we keep temperature below ambient and humidity low, preventing hydrolysis or unwanted side reactions that can limit reliable use downstream.
Colleagues in the laboratory and at scale-up tell us that 1-(Ethoxycarbonyl)Methyl-3-Methylimidazolium Chloride works as more than just a curiosity. Its role as an ionic liquid precursor and functional reagent has real value in organic synthesis, particularly in the development of catalytic systems and as a phase-transfer agent. Some electrochemical teams look for specific cation/anion combinations to modulate conductivity and viscosity or to enhance selectivity in controlled environments. The ethoxycarbonyl group is not just cosmetic — it responds predictably during functional group transformations and can provide useful handles for subsequent derivatization strategies in pharmaceutical, material science, and fine chemical contexts.
For industrial clients scaling up heterocycle chemistry, the reproducibility from batch to batch means less downtime in troubleshooting and fewer deviations in final product quality. We hear from polymer research groups that the unique imidazolium scaffold with its pendant ethoxycarbonyl sometimes acts as a template or spacer that improves polymer chain properties, solubility, or ionic conductivity in new material platforms. Others have found utility in the compound's ability to influence reaction media, opening doors to milder, greener synthetic routes under ionic liquid conditions.
Feedback from partners working at the bench and in production routinely informs adjustments to process controls. Moisture sensitivity is a recurring theme, so our facility prioritizes airtight transfers and high-vacuum drying. Each kilogram delivered is subject to checks for chloride levels, absence of by-products, and residual solvents because chemists downstream often spot these during analysis. We know that a poorly controlled batch can lead to inconsistent yields or even unexpected reactivity in multi-step sequences.
Our in-house product rarely opposes water outright, but extended exposure in humid environments typically leads to gradual color change and testable hydrolysis. For this reason, we always suggest keeping containers sealed, and we monitor for discoloration before products ever leave our warehouse. Collaborating with end users, we have certified long-term storage to typical organic temperature ranges to preserve both purity and clarity.
There are imidazolium compounds available with different side chains or anions, yet 1-(Ethoxycarbonyl)Methyl-3-Methylimidazolium Chloride performs with a distinct balance of organophilic and ionic character. Alternative imidazolium salts without the ethoxycarbonyl-methyl substituent rarely match its compatibility profile in solvent-free or high-salt systems; some common analogs demonstrate stronger hygroscopicity, making handling more challenging in open-air conditions. Others with larger or more electron-withdrawing anions, while useful in purely ionic liquid settings, frequently lose ground in catalytic or direct organic synthesis because they resist certain nucleophilic transformations or behave as inert fillers rather than participants.
Colleagues using our product have pointed out the increased solubility of 1-(Ethoxycarbonyl)Methyl-3-Methylimidazolium Chloride in polar organic solvents compared to bulkier analogs. This makes workup and analytical processes more predictable, especially where clean separation or crystallization is required. Customers have reported improved reproducibility and fewer purification headaches, as recovery from the reaction mixture becomes easier and less prone to emulsion formation or co-precipitation.
Continuous improvement drives our process design. We document every batch, lot, and processing parameter through the plant. Our operators and chemists understand that quality always shows itself in the smallest details: clarity, particle size, absence of undesired crystalline byproducts, and, above all, reliability during customers’ workflows. Applied analytical methods — NMR, IR, elemental analysis, and liquid chromatography — confirm structure and high purity. We welcome feedback and treat customer returns or performance anomalies as immediate learning opportunities, tracing those back to the instrument, raw material supplier, or handling procedure that needs correction.
On several occasions, research groups and industry partners have traced difficult reactivity patterns or inconsistent end-product profiles back to undetected impurities or subtle changes in anion or cation quality. Our experience confirms that no specification sheet alone guarantees identical performance in complex, multi-step syntheses. On-site technical experts handle specific questions about application suitability, safe use, and potential pitfalls. We believe in sharing practical experience — whether related to reactivity highlights or safe disposal — as part of every product shipment.
Transitions from kilogram-scale to larger commercial levels often bring challenges. Customers planning for multi-ton needs require clear communication about timelines, material availability, and expected lot variability. Our hands-on manufacturing team plans overlapping production and maintains sufficient buffer stock to cover unexpected surges or quality reviews that may temporarily stall shipments. Over the past several years, demand has grown from electronics, battery, and fine chemical industries, each with its own profile for purity, color, and contamination concerns.
Plant upgrades to reactors, filtration units, and drying systems have yielded more uniform lots, with stricter process parameters and improved in-plant monitoring. High shear mixers allow better dispersion, eliminating the tendency for stubborn micro-aggregates that often slip through with some less refined imidazolium salts. Handling requirements throughout the chain — from synthesis through to drying and final packaging — stay calibrated to downstream needs. Our commitment lies in giving researchers, formulators, and process engineers a reliable building block to use without repeat troubleshooting for each procurement batch. That’s part of the working agreement between a manufacturer and each customer.
Direct experience with specialty salts, including 1-(Ethoxycarbonyl)Methyl-3-Methylimidazolium Chloride, has shaped our facility’s safety standards. Operators follow protocols to minimize inhalation and skin contact, and work spaces run under local ventilation with rapid response measures on hand for unforeseen spills. We have invested in safe waste-handling and neutralization procedures for both production and cleanup steps, because downstream users must trust that hazardous byproducts or residues never reach them.
We maintain transparency concerning residual solvent content and product trace metals, making relevant batch data available to serious purchasing partners, and offering actual certificate of analysis documents upon shipping. Occupational health teams meet regularly to review product-specific hazards, update labeling in line with new evidence, and demonstrate responsible stewardship of these materials, both within the facility and among the communities we live in.
Moving 1-(Ethoxycarbonyl)Methyl-3-Methylimidazolium Chloride safely from the production line to client lab or factory calls for packaging that resists moisture and maintains chemical stability the entire time. We select HDPE or inert-lined containers fitted with tamper-evident seals; experience warned early on about using less barrier-resistant packaging, which often ended up compromising product on long hauls, particularly in humid or variable climates. Shipping teams work closely with logistics partners to flag these needs and maintain proper documentation to avoid unnecessary customs delays, which only worsen stability and traceability issues.
Stock forecasting aligns with actual ordering trends, not mere projections, which prevents overexposed stock from aging on the shelf and losing value or function. For major academic clients and R&D facilities ordering smaller lots, we prepare secondary sealed vials inside larger canisters, limiting exposure to air or accidental contamination. This method cuts down on loss and has led to higher customer satisfaction on dozens of repeat purchasing programs.
Years of direct engagement with academic and industrial collaborators have taught us the success of a chemical innovation depends not just on purity or competitive pricing, but on transparent problem-solving. When users identify application problems — whether solubility mismatches, unexpected byproducts, or shelf-life drop-offs — we work side by side, reviewing syntheses, handling routines, and formula tweaks. This exchange sharpens our own understanding of both the chemistry and practical realities facing downstream users.
Large multistep projects require dialogue from early development to final application. Regulatory needs sometimes shift faster than anticipated, so we routinely update partners about changes in manufacture protocols or new findings regarding environmental impact. Researchers benefit when manufacturers see themselves as part of a broader technical team, bringing decades of process knowhow and willingness to redirect production if the end use case demands. From coordinating custom purification stages to scaling unique orders, flexible lines and deep domain knowledge often make or break project timelines.
As real-world work reveals shortfalls in stability or performance, we pilot innovations in process chemistry and downstream refinement. For 1-(Ethoxycarbonyl)Methyl-3-Methylimidazolium Chloride, problems with shelf life, hydrolytic sensitivity, and physical handling have driven our R&D teams to experiment with advanced desiccation protocols, anti-caking agents compatible with end-use chemistry, and sealed environment transfer systems. Some performance setbacks lead directly to investment in instrumentation upgrades or alternate purification routes, freeing production from bottlenecks that once limited throughput or raised production costs.
Actions based on concrete data replace old instincts. Product feedback feeds statistical analysis across multiple production campaigns, and decisions draw on both direct experiment and user testimony. At plant level, strict in-line control of pH, temperature, and filtration integrity allow us to fine-tune output and cut down on post-synthesis failures. By embracing direct user feedback, our process engineers continually find ways to reinforce critical control points and stave off future production difficulties.
Effective chemical manufacturing means following each regulatory evolution, not merely for legal compliance, but to protect personnel and customers alike. Tracking regional and international legislation about the use, transport, and disposal of ionic liquids keeps us proactive. We have adjusted formulation and documentation ahead of regulatory change to ensure customers never face needless hold-ups or loss of supply continuity.
Sustainable innovation in imidazolium chemistry points toward greener processing, minimizing high-energy purification and reducing production waste and emissions. Customers tell us that sustainability claims only matter when they translate into actual, measured improvements in product footprint or downstream impact. Our plant tracks energy use and emission profiles from each campaign batch, making improvements whenever practical options arise.
As a producer with regular exposure to new research, we have seen the growing role of 1-(Ethoxycarbonyl)Methyl-3-Methylimidazolium Chloride in diverse fields: from the development of advanced electrolytes in battery technology, to organic phase transfer in synthesis of bioactive molecules, to the creation of responsive materials in electronics and sensors. We interface with specialists from all these domains, recognizing that each sector brings different requirements for reliability, regulatory footprint, and chemical adaptability.
Our batch records, technical staff, and collaborative mindset set us apart from detached bulk suppliers. The best results routinely come from mutual engagement and an honest account of capabilities and limits. Everyday improvements — even the small, incremental ones — compound to deliver a more robust, higher-functioning chemical, giving downstream innovators confidence to commit to projects using these specialty materials.
Years of error, dialogue, and repair go into every kilogram of 1-(Ethoxycarbonyl)Methyl-3-Methylimidazolium Chloride we ship. Starting from raw material selection through to final container seal, our teams balance technical criteria with hands-on knowhow. Each specification comes backed by performance confirmation in dozens of real-world research and production settings, blending our expertise in synthesis, purification, storage, and logistics. The end result is not just a standardized product, but a reliable partner in developing the chemical innovations of tomorrow.