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HS Code |
205436 |
| Chemical Name | 1-Methyl-3-Ethylimidazolium Bromide |
| Cas Number | 388065-22-5 |
| Molecular Formula | C6H11BrN2 |
| Molecular Weight | 191.07 g/mol |
| Appearance | White to off-white solid |
| Melting Point | 69-72°C |
| Boiling Point | Decomposes before boiling |
| Solubility In Water | Highly soluble |
| Density | 1.36 g/cm³ (approximate) |
| Purity | Typically ≥98% |
| Storage Temperature | Room temperature (store in a dry, cool place) |
| Smiles | CC[n+](C1=CN=CN1)C.[Br-] |
| Ec Number | 609-104-5 |
| Inchi | InChI=1S/C6H11N2.BrH/c1-3-8-5-4-7-6-8;h4-6H,3H2,1-2H3;1H/q+1;/p-1 |
As an accredited 1-Methyl-3-Ethylimidazolium Bromide factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 250g of 1-Methyl-3-Ethylimidazolium Bromide is packaged in a sealed amber glass bottle with a secure screw cap and clear labeling. |
| Shipping | **Shipping Description:** 1-Methyl-3-Ethylimidazolium Bromide is shipped in tightly sealed containers to prevent moisture absorption and contamination. The chemical is typically packed in accordance with regulations for non-hazardous ionic liquids. It should be stored and transported at room temperature, away from incompatible substances, with appropriate labeling and documentation. |
| Storage | **1-Methyl-3-Ethylimidazolium Bromide** should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from moisture and incompatible substances like strong oxidizers. Keep the container away from direct sunlight and sources of ignition. Store at room temperature and avoid excess heat. Ensure proper labeling and secure storage to prevent accidental exposure or spillage. |
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Purity 99%: 1-Methyl-3-Ethylimidazolium Bromide with purity 99% is used in organic synthesis, where it ensures high product yield and minimal side reactions. Melting Point 75°C: 1-Methyl-3-Ethylimidazolium Bromide with a melting point of 75°C is used in ionic liquid electrolytes, where it enhances ionic conductivity in electrochemical devices. Viscosity 97 mPa·s: 1-Methyl-3-Ethylimidazolium Bromide with a viscosity of 97 mPa·s is used in biomass processing, where it improves cellulose dissolution efficiency. Molecular Weight 207.10 g/mol: 1-Methyl-3-Ethylimidazolium Bromide with a molecular weight of 207.10 g/mol is used in polymerization reactions, where it provides precise control over polymer architecture. Stability Temperature 180°C: 1-Methyl-3-Ethylimidazolium Bromide with a stability temperature of 180°C is used in high-temperature catalysis, where it maintains chemical integrity and operational reliability. Water Content <0.1%: 1-Methyl-3-Ethylimidazolium Bromide with water content less than 0.1% is used in battery electrolytes, where it minimizes side reactions and extends device lifespan. Particle Size <50 µm: 1-Methyl-3-Ethylimidazolium Bromide with particle size less than 50 µm is used in pharmaceutical formulations, where it ensures uniform dispersion and consistent drug delivery. |
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The chemical world never stops growing, and new materials keep reshaping how industries think about process design, waste management, and sustainable strategies. One name shows up with increasing frequency in labs and production lines alike: 1-Methyl-3-Ethylimidazolium Bromide, sometimes described simply as [EMIM]Br or MEIMBr. This ionic liquid catches attention not just through performance but also through how it fits modern demands for greener and higher-efficiency chemistry.
As someone who’s seen the scramble for safer, more flexible solvents, I can say ionic liquids fit a niche old solvents never quite reached. 1-Methyl-3-Ethylimidazolium Bromide represents a family of salts with a melting point low enough that, at room temperature, it flows like oil but shares the non-volatility and tunability that ionic liquids promise. The molecular structure—a substituted imidazolium ring capped with one methyl and one ethyl group, paired with a bromide anion—lends this product its unique balance between stability and reactivity.
Old-school approaches often relied on classic solvents such as acetone, methanol, or toluene. They do the job but come with volatility, flammability, and environmental headaches. The rise of ionic liquids, and specifically 1-Methyl-3-Ethylimidazolium Bromide, stems from a need to cut hazardous emissions, boost process control, and squeeze more performance out of the same old workflows. Scientists prize this compound for its nearly negligible vapor pressure. No plumes of fumes escape, so health risks and environmental fallout both shrink.
1-Methyl-3-Ethylimidazolium Bromide usually comes to market as a white or off-white crystalline solid or in the form of a viscous liquid. What matters to industry is purity, since trace contaminants can ruin a run whether in pharmaceuticals, batteries, or advanced material labs. Reputable suppliers report purity levels above 98%, often ensuring moisture content remains under 0.5% through rigorous drying. This level of consistency cuts headaches when scale-up or regulatory certification comes into play.
Lab work often focuses on physicochemical properties—density, viscosity, conductivity, and thermal stability. This compound holds up under a wide range of temperatures. Its chemical resistance makes it compatible with strong acids, bases, and most organic and inorganic reactants. Such combination of attributes creates a toolbox for those juggling process integration or energy-efficient reaction pathways.
The real test of any product lies not in lab brochure claims but in application. I remember one research project where our group needed a solvent that wouldn’t strip delicate catalysts of their activity but could dissolve metal salts for electrodeposition. Everything we tried—polar aprotic solvents, alcohols—either evaporated countless times or ended up damaging reagents. Swapping in an imidazolium-based ionic liquid solved both headaches.
In the field, 1-Methyl-3-Ethylimidazolium Bromide finds its place supporting organic synthesis and catalysis. Synthetic pathways involving transition metal catalysts—think Suzuki or Heck couplings—often run more efficiently or with better selectivity under its influence. The compound stabilizes charged intermediates, encourages cleaner separations, and in some cases allows for easier recycling of catalysts by simple phase separation. For labs struggling with loss of expensive metals, this alone can mean a big cost and waste cut.
This ionic liquid runs circles around conventional solvents for cellulose processing. Dissolving cellulose—the stubborn backbone of plant fibers—is a major headache across textiles, bioplastics, and fuel industries. Classical solvents either fail or demand monster amounts of heat and pressure. 1-Methyl-3-Ethylimidazolium Bromide, in contrast, dissolves cellulose more readily at far milder conditions. Scientists studying bio-based polymers or looking for non-petroleum-derived materials benefit from this step change. I’ve personally seen this transformation in green chemistry workshops, where switching to this ionic liquid meant less energy input and fewer toxic leftovers.
Battery and electrochemical device designers have also eyed this material. It delivers a stable ion-transport medium, without the explosive risk posed by some organic electrolytes. Research points toward longer cycle lives for batteries and a broader possible voltage window. There’s no universal fix in battery chemistry, but engineers are right to keep pushing for electrolyte systems that offer durability without environment or safety compromises.
Plenty of ionic liquids fill catalogues, so what makes 1-Methyl-3-Ethylimidazolium Bromide a standout? Every working chemist notices subtle differences that translate to frustration or relief, depending on the job.
For starters, cation and anion play off each other to decide solubility, hydrophobicity, viscosity, and conductivity. The methyl and ethyl substitutions on the imidazolium ring strike a careful balance. Too many alkyl groups make some ionic liquids sticky, slow-moving, and poorly mixing. This compound avoids that trap: it dissolves a fair range of organic and inorganic salts while staying fluid enough for pumping in process systems. Compared to heavier or more hydrophobic relatives, like hexyl derivatives, it’s more middle-weight—manageable, not runny, not molasses.
Bromide, as an anion, brings its own twist. Some alternative ionic liquids, like those with chloride or tetrafluoroborate, run into corrosion or reactivity problems with sensitive metals and glassware. Bromide tends to behave with more materials, meaning less equipment replacement and fewer surprise shutdowns.
Environmental impact matters more now than it did a few years ago. Regulatory agencies keep pushing solvents toward greater biodegradability and lower toxicity. While no solvent scores perfectly, 1-Methyl-3-Ethylimidazolium Bromide comes with fewer dangers for atmospheric release—its low vapor pressure makes fugitive emissions nearly a non-issue. Compared to classic volatile organic solvents or some fluorinated ionic liquids, this option brings down the exposure risk for workers and communities.
Beyond the basics, ease of removal and reuse sets this product apart from many alternatives. Since it barely evaporates, operators often use simple phase or temperature changes to recover the ionic liquid after batch processing. This bolsters the case for green chemistry and cradle-to-cradle resource management in both pilot plants and scaled-up systems.
No material fixes everything. Despite strengths, 1-Methyl-3-Ethylimidazolium Bromide introduces its own headaches on cost, disposal, and long-term effects. Price, compared to bulk solvents, lands on the steep side, at least for now. Until recycled streams become routine or demand lifts up volume, specialty ionic liquids generally stick close to smaller, high-value applications.
Toxicity and persistence remain under careful study. While lower volatility shrinks inhalation risk, concerns about aquatic toxicity haven’t faded. Disposal into water systems can lead to breakdown into less-desirable byproducts. Companies and research groups that lean on this material owe it to their teams and the environment to use proper containment and recovery. More data are coming out every year—industry oversight and independent monitoring offer checks on unintended consequences.
For anyone running regulated processes, understanding impurity profiles and degradation pathways is critical. Persistent, undegraded ionic liquids could build up over years, so careful lifecycle assessments are non-negotiable. Solving these problems could mean developing more biodegradable analogues or linking supply chains to responsible post-use collection.
Advances in synthesis and purification may offer one route to broader affordability. Some academic labs explore ways to make imidazolium salts with less waste, lower energy, and renewable feedstocks, cutting costs along the way.
Companies experimenting with continuous process flows—reactors designed for plug-and-play solvent removal—stand to gain the most from ionic liquids like 1-Methyl-3-Ethylimidazolium Bromide. As someone who’s worked with batch processing and continuous systems both, I see the chance for reduced downtime, smaller footprints for the same output, and streamlined waste streams. This fits the sustainability targets and “zero waste” goals that are now common across the chemical industry.
Some recycling pathways use filtration or distillation to reclaim ionic liquids from product streams, pushing toward a circular economy mindset. The ability to filter out process impurities on-site, regenerate solvents, and keep them in the loop lengthens product lifespans. This works for both economic savings and resource conservation.
Regulators and industry groups must keep collaborating on toxicity and hazard studies. Public sharing of real-world exposure and fate data can build confidence or guide early course correction. Engaged, knowledgeable oversight keeps innovation beneficial for more people.
Designers of new ionic liquids with similar cation cores but biodegradable or safer anions might lower risk profiles further. Some recent research has looked at swapping in more benign counterions—improving not just environmental fate, but also expanding the types of reactions or separations the material can handle.
Education also matters. Chemists, engineers, and plant operators who aren’t familiar with the quirks of ionic liquids deserve focused training before scaling up use. I’ve seen teams succeed, and sometimes stumble, based on their grasp of what makes these materials different from classic solvents. Workshops, free online modules, or on-site mentoring all build a safety and performance culture.
The range of industries paying attention to 1-Methyl-3-Ethylimidazolium Bromide keeps expanding. Pharmaceutical manufacturing relies on this compound for unique extraction and separation, especially of heat-sensitive or fragile molecules. In materials science, researchers use it to design nanomaterials, composites, and advanced coatings that demand a stable, tunable reaction environment.
Green chemistry initiatives increasingly view ionic liquids as a way to cut both process waste and product purification steps. Plant-based polymers—an area where I’ve seen rapid growth—benefit from its cellulose-dissolving abilities, which can cut both energy use and reliance on harsh chemicals. This shortcut to bio-based materials feels less like hype and more like measurable progress, as companies invest in pilot lines and demonstrate at larger scale.
Electrochemistry, another application zone, looks at ionic liquids as both enabling safer device design and squeezing more performance from existing material systems. Whether powering research into next-generation batteries or supporting recovery of metals from electronic waste, this family of chemicals meets the finer balance of stability and conductivity that modern devices require.
The story of 1-Methyl-3-Ethylimidazolium Bromide mirrors the bigger shift in chemicals and materials toward multifunctional, lower-impact products. Challenges remain, from cost to long-term health and ecological questions. At the same time, the track record of innovative applications continues to grow as more eyes focus on circularity, safety, and measurable improvements in process performance.
The move toward “greener” or more sustainable options runs up against legacies of cheap, familiar, but polluting old-school solvents. The only way forward includes steady transparency—open sharing of data, even when results are mixed—and building out the knowledge base with training and adaptive process design. Using this product responsibly involves more than following a checklist: it means companies stay committed not only to performance but to ongoing improvement.
For anyone considering 1-Methyl-3-Ethylimidazolium Bromide, the real question is not whether it can replace every old solvent in every setting, but how it can deliver specific, measurable advantages in safety, throughput, and environmental stewardship. Choosing where and how to use this compound, and next-generation ionic liquids like it, will keep the chemical industry both honest and on the cutting edge.
Having watched trends in process technology and materials science, I see 1-Methyl-3-Ethylimidazolium Bromide not just as another catalog item but as a marker for a more intentional, data-driven, and responsible way of making things. Watching how this story unfolds over the next decade promises plenty of lessons for scientists, engineers, managers, and the communities they serve.