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HS Code |
154996 |
| Chemicalname | 1-Benzyl-3-Methylimidazolium Chloride |
| Casnumber | 153210-50-9 |
| Molecularformula | C11H13ClN2 |
| Molecularweight | 208.69 g/mol |
| Appearance | White to off-white solid |
| Meltingpoint | 75-80 °C |
| Solubility | Soluble in water and polar organic solvents |
| Boilingpoint | Decomposes before boiling |
| Density | 1.18 g/cm3 (approximate) |
| Purity | Typically ≥98% |
| Iupacname | 1-benzyl-3-methyl-1H-imidazol-3-ium chloride |
| Storageconditions | Store at room temperature, tightly closed, in a dry place |
As an accredited 1-Benzyl-3-Methylimidazolium Chloride factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Supplied in a 100g amber glass bottle with tamper-evident cap, labeled with chemical name, hazard symbols, and safety information. |
| Shipping | 1-Benzyl-3-Methylimidazolium Chloride is shipped in tightly sealed containers, protected from moisture and light. The package adheres to regulations for transporting chemicals, including appropriate hazard labeling. It is typically dispatched via ground or air freight, with handling precautions to prevent spills or exposure due to its potential health and environmental hazards. |
| Storage | 1-Benzyl-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. Keep it away from direct sunlight and sources of ignition. Ensure proper labeling and avoid prolonged exposure to air to prevent degradation or absorption of water, as it may be hygroscopic. |
Applications of 1-Benzyl-3-Methylimidazolium Chloride in Industrial ManufacturingAs a manufacturer of 1-Benzyl-3-Methylimidazolium Chloride, we supply this ionic liquid to multiple specialized sectors requiring advanced chemical performance. Our direct integration into downstream manufacturing ensures traceability and tailored control over purity, particle size, and packaging for complex industrial applications. Below are the principal industrial routes and use cases with sector-specific implementation details. 1. Homogeneous Catalysis for Fine Chemical Synthesis1-Benzyl-3-Methylimidazolium Chloride acts as a non-volatile ionic liquid solvent and a phase-transfer catalyst base during demanding multi-step synthesis, including Suzuki coupling and Heck reaction. Chemical manufacturers utilize it for improved catalyst stability, enhanced selectivity, and minimal organic emissions. The product supports both batch and continuous flow routes involving transition metal complexes and functional aryl halides. Chemists closely define the solvent system to control activity and prevent catalyst leaching, further optimizing for high-value building blocks in pharmaceutical and agrochemical intermediates. Industry compliance standards
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2. Electrolyte Additive for Electrochemical DevicesDownstream manufacturers of dye-sensitized solar cells, high-temperature batteries, and capacitors use this ionic liquid as a component of advanced non-aqueous electrolyte systems. The chloride anion and stable imidazolium cation give wide electrochemical windows, enhancing ion conductivity and device shelf life. The product maintains performance under broad temperature and voltage ranges, integrating into proprietary liquid blends to ensure safety and cell cycling stability. Strict trace metal and water content controls are critical throughout the blending and filling process to match device QC requirements. Industry compliance standards
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3. Solubilization Agent in Biomass Conversion and Lignocellulosic ProcessingIndustrial bio-refineries and cellulose material processors use this ionic liquid as a specialized solubilizer and reaction medium for efficient lignin dissolution from wood, straw, or bagasse. The product’s cationic structure disrupts strong hydrogen bonding in lignocellulose, facilitating enzymatic or chemical conversion to fermentable sugars and platform chemicals. Operators fine-tune loading to balance biomass dispersion and downstream hydrolysis, supporting closed-loop solvent recovery for process economics and environmental compliance. Industry compliance standards
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4. Organic Synthesis Intermediate for Quaternization and Ionic Liquid DevelopmentChemical processors involved in the production of novel ionic liquids and quaternary ammonium compounds use this raw material both as a source of the imidazolium cation and as a building block for derivatization through customized quaternization reactions. Its high reactivity and defined structure make it suitable for direct transformation with various alkyl groups, halides, or functional moieties, matching the synthesis requirements for specialty solvents, ion-exchange resins, and customized separation agents. Quality assurance emphasizes NMR, HPLC, and Karl Fischer water determination for batch release. Industry compliance standards
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Chemistry keeps moving forward, and the materials used in research and industry shape the speed of progress. In our factory, we've watched the rise of ionic liquids change routines that used to depend on volatile organics or salts that left messes behind. 1-Benzyl-3-Methylimidazolium Chloride has earned a place on our workbenches by bridging the gap between traditional solvents and cutting-edge green chemistry needs. Our job is to make sure you get a material that lives up to its reputation—batch after batch, shipment after shipment. What sets this compound apart is its remarkable flexibility in synthesis, extraction, catalysis, and new-generation electrochemical work. These are not hollow claims, but conclusions drawn from years of production feedback, test data, and customer experience.
Labels can run together when you compare compounds with long chemical names or similar-looking structures. This salt stands out for specific reasons, and it’s worth describing not just with a name but through lessons learned from tanks, reactors, and drying trays.
This compound consists of a benzyl group bonded to a methylimidazolium ring, paired with a chloride anion. In physical terms, it appears as a faintly off-white to white solid at room temperature, showing high moisture affinity—a trait handled in our sealed environments and confirmed through regular Karl Fischer titration and loss-on-drying runs. Our QC team rarely needs to tweak procedures, as this compound is less susceptible to hydrolysis than other chloride-based salts. That stability saves a lot of troubleshooting both here and downstream in your lab or production.
With many ionic salts, product performance hinges on residual contaminants and water content, rather than headline purity percentages. Feedback from users running organometallic catalysis or solvent extractions often points to low ppm-level halide impurities as the most decisive feature. We wash and recrystallize our product several cycles, carefully avoiding reagent cross-contamination, confirmed by NMR and ion chromatography every step along the way.
Other ionic liquids, like 1-butyl-3-methylimidazolium chloride, often show more variability batch-to-batch, mostly due to hydrolysis or side reactions at their less bulky alkyl chains. By contrast, the benzyl group present in 1-benzyl-3-methylimidazolium chloride remains more robust during both manufacture and downstream usage. Even researchers running high-throughput screening or repeated catalysis cycles comment how clean the work-up stays, with easier separation of organic and aqueous phases and fewer issues with emulsion.
From the production angle, the role this compound plays in green chemistry is more than a talking point. We have received plenty of research notes and process plant feedback on its use in Suzuki, Heck, and other palladium-catalyzed couplings. In many cases, reactions that stumble in traditional solvents move along briskly in the presence of this chloride salt as the solvent or phase-transfer catalyst. Customers running nucleophilic substitutions or ionic-liquid-based biphasic systems find the product brings higher conversion and cleaner separation at the back end.
We see demand spike from labs extracting rare earths and heavy metals too, since the product’s structure allows it to solubilize and separate a range of cations and anions. The benzyl group increases solvent power for complex organics, compared to more basic imidazolium salts, translating into higher extraction capacity per gram and easier recovery during recycling. These are points that show up not only in academic literature but in purchase requests and scale-up discussions as users shift away from classic chloroform or other hazardous solvents.
Ionic conductivity ranks among the top reasons users switch over to this kind of salt in battery research and electrochemical sensors. In-house, our technical staff keep an eye on conductivity using defined electrode setups: consistently, this benzyl-methylimidazolium chloride delivers higher ionic mobility in molten or highly concentrated aqueous systems than many smaller-cation salts.
The difference unfolds in practical experiments: fewer stability issues at higher voltages, better resistance against oxidation, and longer test cell cycles. As more groups move toward next-generation batteries—whether lithium, sodium, or flow cell technology—the advantages in thermal stability and electrochemical window continue to drive demand for this product.
Our experience making this compound offers a unique perspective on what sets it apart from other imidazolium salts. For one, the presence of the benzyl group not only brings steric bulk but also lets users fine-tune the hydrophobicity and dissolution properties of both cations and counterions. The chloride anion provides solid compatibility with a wide array of metals and is easily removed or exchanged if needed during downstream chemistry.
Other salts, such as 1-butyl-3-methylimidazolium chloride, come with a different cost and availability profile but are less reliable for process chemists seeking high selectivity and minimal cross-reactivity. Methyl-methylimidazolium or ethyl variants often deliver lower solubility for certain organic substrates, making them less suitable for specific extraction or catalysis applications. In our own blending and stability tests, the benzyl derivative exhibits lower volatility and reduced aldehyde or ketone byproduct formation over long storage periods.
Many labs and pilot plants prefer small-scale sampling, while others need drums or bulk lots for multi-step synthesis. We have refined our batch sizing to cover everything from a few hundred grams to several hundred kilograms, using inert-gas packaging and moisture-proof liners. This logistical preparation results from experience—materials like 1-Benzyl-3-Methylimidazolium Chloride are so hygroscopic that a moment’s lapse in handling can push water content out of accepted range, affecting everything downstream for users focused on catalytic conversion or precise analytical work.
Feedback from long-term users tells us packaging matters just as much as purity or batch traceability. Some groups request single-use containers to avoid potential cross-contamination; others want returnable bulk vessel programs to cut plastic waste. We adjust to these needs, always keeping inventory turnover quick, because even the best-quality product will suffer from long-term exposure, even in a sealed warehouse.
Scaling up from kilogram to multi-tonne production rarely goes straight as planned. We have tackled issues from pump crystallization, gumming in transfer lines, and reactor fouling—each event teaching us new tricks in minimizing hold-up, ensuring proper drying, and confirming batch uniformity. This sort of hands-on learning shifts from textbook theory to practical reality as soon as the first crystals hit the filter.
Our technical team has trained on moisture reduction techniques and optimized off-gas scrubbing to minimize both product degradation and unwanted side reactions. We keep a line of communication between the production floor and technical sales, since customer feedback often turns into improved process specs or new grades. The fact that most citations and process patents referencing this salt emphasize its reproducibility matches what we see working on our reactors and dryers—consistency comes from obsessive process refinement, not just raw starting ingredients.
Reducing solvent waste remains a goal for every chemical manufacturer with an eye on future regulations or internal cost controls. Supplying 1-benzyl-3-methylimidazolium chloride means fielding a steady stream of questions: What does it take to recover it after use? Are there disposal problems? Can it be safely neutralized?
Our process focuses on maximizing feedstock recovery and recycling. The product’s chemical robustness means most users enjoy repeated use, cutting down on waste disposal costs. Acid and base resistance matches or exceeds most traditional quaternary ammonium salts; byproducts break down with less generation of problematic halogenated volatiles. These are not trivial points given the number of labs and plants now facing stricter guidelines on halide disposal and atmospheric release.
We have found ourselves in close touch with R&D teams exploring specialized extractions, bio-catalysis, and selective separations. After extensive back-and-forth on optimal particle sizing, drying endpoints, or impurity removal, it normally comes down to this single trait: does the reagent perform under pressure? The benzyl substitution provides expanded compatibility and less interference during high-throughput applications, enabling continuous runs in pharmaceutical syntheses and polymerizations where trace contamination or reactivity matters more than headline purity specs.
Some pharmaceutical chemists highlight the material’s mild base resistance, allowing for safer downstream modifications without needing extensive neutralization steps. In the realm of material science, this salt supports easier template formation in porous frameworks and zeolites, because it resists decomposition under standard synthesis conditions. This kind of hands-on verification, echoed in the academic and patent literature, validates our operational improvements and customer advice.
The chemical manufacturing sector shifts constantly in response to changes in regulatory landscapes and evolving industrial priorities. Over the years, we’ve watched more projects focus on lowering toxic solvent use and increasing recyclability. We field queries surrounding compliance in shipping, handling, and storage, with more requests for documentation than ever before. While our own operations use best-practice handling for hazardous materials, we encourage all users to adopt the same standards, keeping material loss, cross-contamination, and waste minimization central to their process flows.
Whether for an academic bench top or an industrial bulk process, this chloride salt supports a move towards more controlled, closed-system processing, letting users cut exposure and venting. By responding promptly to new environmental and handling requirements, we help researchers and plant engineers stay ahead instead of playing regulatory catch-up.
Once a shipment leaves our warehouse, it enters a chain of handling over which we often lose direct control. That said, the bulk of quality issues traced back to the beginning usually point to excessive moisture uptake, jar residues, or improper storage. By investing in better humidity control and packaging upgrades, we cut these risks from the start. For long-term partners, we also offer batch reserves in climate-controlled storage, so you never have to worry about drawing from stale or compromised material months down the line.
We follow up with users not only at the point of sale but months and years afterward, getting first-hand accounts on shelf stability and in-use performance. This feedback lets us refine both our manufacturing approach and our advice to customers, so their chemistry keeps pace with expectations, regardless of shifts in supply chain or project scope.
Manufacturers of specialty chemicals like 1-Benzyl-3-Methylimidazolium Chloride often hear only about price-per-kilo or lead times as decision points. From our perspective, the reality is much more nuanced. End uses in fine chemistry, electronics, or environmental analysis demand more than a low-cost product—they require reliability, transparency, and a long-term partnership.
Supporting customers through occasional troubleshooting, batch recalls, or customized formulations anchors our daily work. Our experience has taught us that open channels and a real willingness to adjust production parameters distinguish manufacturers who care about end results from those who simply move boxes. Longer shelf-life, real traceability, and honest advice about best-use conditions matter far more to innovative chemists than a quick lowball price.
Future research looks promising for this compound, given growing attention in next-generation battery technologies, greener catalysis, and enhanced analytical separation processes. Our willingness to co-develop new variants, optimize particle sizes or create bespoke formulations helps scientists and engineers set new standards for performance. The benzyl-imidazolium scaffold remains robust enough for creative experimentation while providing a familiar starting point for tuning properties.
We encourage users to share new needs and report any unexpected handling or performance observations. Our production facilities remain ready to scale, adjust, or develop new approaches—reacting not to market noise but direct demand from experienced chemists who know exactly what they want from their materials partner.
After years perfecting the processes behind 1-Benzyl-3-Methylimidazolium Chloride, we have witnessed its strengths and limits firsthand. For us, supplying this compound extends beyond just quality assurance or on-time delivery; it's about ensuring that smart, reliable materials underpin every reaction, extraction, and analysis that moves your research or production closer to success.
We believe the best chemistry starts with high-quality, consistent, and honestly-made materials. That is our commitment on every batch, and the standard we hold for every partnership, whether you are developing the next green catalyst, scaling a novel separation, or simply aiming for cleaner, safer, more effective lab work.