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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 | 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. |
Applications of 1-Carboxymethyl-3-Methylimidazolium Chloride in Industrial Manufacturing1-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 ProductionLeading 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
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2. Electrolyte Formulation in Lithium-Ion Battery ManufacturingBattery 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
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3. Homogeneous Catalysis for Esterification and TransesterificationChemical 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
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4. Biomass Pretreatment for Second-Generation BiofuelsBiofuel 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
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5. Green Solvent for Pharmaceutical API SynthesisAPI 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
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6. Additive for Anti-Static Polymer CompoundingManufacturers 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
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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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.