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HS Code |
549336 |
| Product Name | 1-Butyl-2,3-Dimethylimidazolium Bromide |
| Cas Number | 119002-98-5 |
| Molecular Formula | C9H17BrN2 |
| Molecular Weight | 233.15 g/mol |
| Appearance | White to off-white crystalline powder |
| Melting Point | 90-95°C |
| Solubility In Water | Soluble |
| Boiling Point | Decomposes before boiling |
| Purity | Typically ≥98% |
| Density | 1.3 g/cm³ (approximate) |
| Storage Conditions | Store in a cool, dry place |
| Synonyms | [BM2Im]Br; 1-Butyl-2,3-dimethylimidazolium bromide |
| Smiles | CCCCn1c(C)nc(C)n1.[Br-] |
| Ec Number | N/A |
| Hazard Statements | May cause skin and eye irritation |
As an accredited 1-Butyl-2,3-Dimethylimidazolium Bromide factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 1-Butyl-2,3-Dimethylimidazolium Bromide is supplied in a sealed 100g amber glass bottle, with tamper-evident cap and safety labeling. |
| Shipping | 1-Butyl-2,3-Dimethylimidazolium Bromide is shipped in tightly sealed, chemically resistant containers to prevent moisture and contamination. It is transported according to standard chemical safety regulations, including proper labeling and documentation. The package avoids excessive heat or sunlight and typically complies with both national and international shipping guidelines for non-flammable, low-toxicity chemicals. |
| Storage | **1-Butyl-2,3-dimethylimidazolium bromide** should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from moisture and direct sunlight. Keep it separate from incompatible substances such as strong oxidizers. Store at room temperature and avoid exposure to excessive heat. Properly label the container and follow all applicable safety regulations when handling and storing this chemical. |
Applications of 1-Butyl-2,3-Dimethylimidazolium Bromide in Industrial Manufacturing1-Butyl-2,3-Dimethylimidazolium Bromide is a high-performance ionic liquid widely employed in advanced chemical processing due to its excellent thermal and chemical stability, adaptable solvation properties, and proven role in challenging separation and catalysis environments. The following application scenarios highlight real industrial uses, focusing on specific requirements and integration points that reflect our direct manufacturing expertise. 1. Cellulose Dissolution for Fiber SpinningSpecialty fiber producers rely on this ionic liquid as a powerful and selective solvent for cellulose, enabling regeneration of high-purity cellulosic fibers for technical textiles and filtration media. Its miscibility and low volatility allow continuous solvent recovery, making the process efficient and environmentally favorable compared to traditional viscose methods. Industry compliance standards
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2. Homogeneous Catalysis for Alkylation ReactionsFine chemicals manufacturers employ 1-Butyl-2,3-Dimethylimidazolium Bromide as a polar reaction medium and phase transfer agent, boosting yields and selectivity in alkylation of aromatic and heterocyclic compounds. Its low vapor pressure improves worker safety and minimizes air emissions compared to volatile organic solvents. Industry compliance standards
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3. Electrolyte Component in Metal ElectroplatingElectronics fabricators and custom plating shops integrate this ionic liquid as an advanced electrolyte medium for controlled deposition of metals such as copper, gold, and nickel onto precision components. The material provides a wide electrochemical window and stable plating characteristics, improving layer uniformity and reducing pinhole defects in electronic connectors and microelectrodes. Industry compliance standards
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4. Extraction of Lignin and Hemicellulose from BiomassLignocellulosic biorefineries utilize this ionic liquid for efficient fractionation of woody biomass, selectively solubilizing lignin and hemicellulose while leaving cellulose largely intact. Controlled process conditions minimize degradation, ensuring high-purity lignin streams for further chemical valorization. Industry compliance standards
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5. Solvent for Transition Metal Catalyzed Cross-Coupling ReactionsLeading pharmaceutical and agrochemical manufacturers use this ionic liquid to enable high-yielding Suzuki, Heck, and Buchwald–Hartwig coupling reactions, where its polarity and ability to stabilize reactive intermediates lead to superior conversion and byproduct reduction compared to traditional DMSO or DMF solvents. Industry compliance standards
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Over years of developing ionic liquids, few compounds handle the job like 1-Butyl-2,3-Dimethylimidazolium Bromide. Our team continues to refine synthesis methods, always looking for purer product and reliable performance. As direct manufacturers, every batch passes through our hands, tested both for residue and moisture, which can quietly undermine sensitive processes down the line. We understand the importance of real consistency; customers rely on this for tight operations, whether they are scaling up fine chemicals or running research experiments.
The molecular structure—a butyl chain on the imidazole ring, flanked by two methyl groups—gives it unique properties among ionic liquids. The design isn’t arbitrary. Over years, industrial and academic partners come back reporting that this cation, paired with bromide, often solves solubility headaches that sulfonate or larger anions can’t touch. Our customers often highlight the stability in various solvents and its manageable viscosity.
Chemists working on separation techniques—extractions, liquid-liquid systems—trust this salt for phase transfer efficiency. Those in catalysis appreciate not just the thermal stability, but also the way side reactions drop when using the right ionic medium. Some spend weeks troubleshooting salt precipitation or breakdown with cheaper brands. They come to us looking for minimal water content and a transparency in the purification record.
In electrochemistry, the fine-tuned ionic mobility surfaces as a real benefit. Battery and supercapacitor developers find it easier to deal with 1-Butyl-2,3-Dimethylimidazolium Bromide compared to alternatives that either gel too quickly or react unpredictably with electrode coatings. In biomass processing, where corrosivity and byproduct formation present continuous headaches, this ionic liquid’s combination of mildness and selectivity often offers a common-sense solution.
On the academic side, this bromide salt winds up in journals investigating hydrogen bonding, proton transfer, and the energetics of non-traditional solvents. We’ve supported phosphate handling, cellulose dissolution, and biofuel model systems—all relying on the reproducibility of a carefully distilled intermediate like 1-Butyl-2,3-Dimethylimidazolium Bromide.
Lab-scale recipe sheets don’t mention how a single contaminated drum can throw off results. We spend extra time cleaning reactors, scrubbing product in the right sequence of solvents, and dialing in vacuum drying so traces of water and halides never become someone else’s headache. Though theoretical min-maxes appear in publications, scaling up production surfaces different issues. Reagents sometimes show batch variance, and heat control in kiloliter reactors demands vigilance. We have learned the true test of our product comes when an entire kilo lot runs without hiccup in a pharma pilot plant—yielding the same reactions and properties as worked out in lab glassware.
Our batches come with full origin tracks. Chemists want more than purity, they want to know about the chain of custody, starting back from base imidazole and the source of each alkylating agent. Too many stories in this field begin with a missing step in documentation or ambiguous impurity spikes—ways to ruin a week’s worth of synthesis without warning. Our operations emphasize this transparency: records are real, not simply printed to appease a checklist. Every certificate means that a technician recorded the date, weighed out the batch, and flagged any deviation along the way.
This chemical does not behave like common salts. It absorbs moisture from air, and it responds to residual acid or base like a sponge reacts to water. Our warehouse storage follows strict protocols: sealed drums, inert atmosphere whenever possible, rapid bottling. Customers storing these salts for more than a few weeks must avoid letting open containers idle in humid labs. The crystalline appearance can mask incipient clumping, and extended air exposure leads to masked alterations in melting range. Such small mistakes don’t always register until a troubleshooting session reveals an altered trace ion profile, or disproportionate color in a final product that cannot be easily washed away.
We recommend decanting only the amount needed for a week’s use, and avoiding unnecessary opening and closing of the stock container. Drying protocols before use take on outsized importance, and many of our regular clients request oven-dried material. For high-throughput syntheses, this simple precaution prevents chronic batch-to-batch inconsistencies. Each misstep avoided represents a saving in both material cost and time—something we, as manufacturers, appreciate directly in our own pilot runs.
Side-by-side with other imidazolium bromides, the profile of the 1-butyl-2,3-dimethyl derivative stands out for several concrete reasons. The presence of methyl groups at the 2 and 3 positions subtly changes hydrophobicity and steric profile compared to basic 1-butyl-3-methylimidazolium bromide or its analogs. In partitioning experiments, this means the compound dissolves certain organic substrates more readily, while resisting phase separation issues at higher ionic strengths. Researchers transferring established methods from more traditional C4 imidazoliums sometimes note cleaner baseline signals and fewer extraneous peaks by switching to this variant.
While some may claim all imidazolium variants offer comparable performance, regular users in demanding syntheses have a different view. The properties of each salt reflect the intricate interplay of molecular structure with target molecule, temperature, and solvent. Subtle issues—like increased foaming, altered surface tension, or the creeping buildup of colored byproducts—plague cheaper or mass-market alternatives. In ionic liquid catalysis, these details spell the difference between smooth project delivery and week-long troubleshooting cycles.
Those who have handled bromides with broader hydrophilic-lipophilic profiles often complain of variable precipitation and difficulty in post-reaction separation. By contrast, the butyl-2,3-dimethylimidazolium bromide salt manages a balance that often lets processes proceed without major tweaks to solvent composition or extraction conditions.
Purity matters, but so does the form in which the product arrives. Our 1-Butyl-2,3-Dimethylimidazolium Bromide product typically comes as a crystalline solid, but we remain vigilant for oiling or clumping that occasionally turns up following prolonged warmth or improper shipping. Particle size variation—an overlooked source of headaches for high-throughput automation—gets checked and logged. Melting point and residual solvents are evaluated against real-world method requirements, not just textbook ideals. On request, we supply pre-dried, sieved, and freshly packed material, since inconsistent bulk material can ruin automated loading and batching.
For customers requiring full traceability, we maintain logs for every packaged lot, linking back to batch start time and the analytical data. We understand the importance of honest reporting—no product leaves our facility without having passed full NMR and Karl Fischer tests, and we don’t cut corners if a batch failed initial inspection.
Rarely does a customer call about a straightforward problem solved by a search engine. The real challenges come from methods scaling unpredictably or reactions not behaving the same from month to month. Plain tables with statistically impressive numbers can’t explain every inconsistency. As builders of both product and process, our team learned to ask deeper questions: Has the base starting material changed source? Are there temperature gradients during storage and loading? Are the cleaning protocols for glassware maintained consistently?
We work directly with several partners to narrow down sources of error. Sometimes, what seems to be a new issue is really a subtle drift in feedstock composition, or a missed check during packaging. Scaling from gram to kilo runs brings unexpected thermal effects—product pooling, local overheating, vapor loss. Our manufacturing experience led us to invest in real-time monitoring and better data logging during every run. The result is not simply fewer surprises, but more conversations based on specifics, not guesswork.
Over a decade refining ionic liquids, trends emerge around 1-Butyl-2,3-Dimethylimidazolium Bromide that academic papers don’t always capture. The most efficient users rarely stick to one method; they adapt, swap out feedstocks, tweak ambient conditions, and make calls for pre-dried or ultra-pure product directly. We respond by iterating our purification setup—changing column packing or switching to freshly distilled bromide sources for certain batches—so customers can count on reproducibility even as their requirements shift.
Regulatory pressure sometimes forces us to maintain stricter impurity profiles or change suppliers at short notice. Instead of passing these complications onto the user, we adapt SOPs to insulate downstream users from variability. Only by running our own plant do we see how much these operational pivots matter. It means occasional overtime and extra QC checks, but outsized rewards in loyal repeat business.
Recurring environmental and handling concerns around bromide and imidazolium salts do not escape our attention. Bench-top use and industrial-scale deployment both draw scrutiny from regulatory offices. In manufacturing, strict ventilation and containment prevent fugitive emissions from contaminating workspaces or outside air. Drums move under internal vacuum, and spills are not tolerated.
Those using the product for extended research must weigh the lifecycle of spent material. We encourage recycling wherever feasible. Through solvent exchange or decomposition systems, bromide can sometimes be recovered, closing the loop for research facilities and pilot plants. Shared responsibility for end-of-life product handling reduces both real and regulatory risk.
We have seen the kind of issues that come from bulk shipments sitting in ports too long, or from departing too long from validated suppliers for reagents. These details add up: a seemingly small impurity, or a week of humidity uptake, can derail productive syntheses. For sensitive users, we always pack inert or nitrogen-purged shipments, and batch-test for unexpected halide fluctuation before shipping. Our longest-standing research partners track lot histories and audit our records, knowing from decades in the field just how easily a supply chain mishap can undo progress.
A pound of material with perfect analysis is no good if it arrives clumped, mislabeled, or full of fine debris from broken packaging. Most customers need clear, granular documentation that matches what actually ships. We keep hands-on oversight by maintaining direct custody over packaging and storage, only releasing stock batches with recent data and cross-verified logs.
Experiences in scaling and direct synthesis shape how we view every product. Feedback and returns don’t fall into a nameless black hole. Each production hiccup—delayed reaction, off-color material, or unscheduled downtime—teaches lessons that inform future batches. Buyers seeking better reproducibility or who are moving to GMP or validated process environments reach out after repeated frustrations with resellers. They quickly learn the difference between dealing with a trading desk and sourcing directly from the plant.
Our history reduces the need for constant oversight. The reassurance comes not from words printed on certificates, but from predictable, tangible results in the users’ own labs. This only happens after years building trust with hands-on handling, responsive communication, and transparent response to unplanned deviations.
Demand for imidazolium-based salts grows as industries search for greener alternatives to volatile organics and traditional halides. Projects on carbon capture, fuel cells, and next-generation energy storage systems drive ever-more attention to stability profiles and lifecycle impact. With users probing deeper and performance thresholds pushing upward, only those with a rigorous manufacturing base keep pace.
We invest in new reactor technologies, improve analytical capabilities, and keep lines of communication open with customers worldwide. This discipline allows us to foresee—not just react—to shifting market and research requirements. The process is never simple, nor free of surprise, but yields a product hard to match in both laboratory trial and plant-scale rollout.
Through years of commitment and occasional recalibration, the defining feature of our 1-Butyl-2,3-Dimethylimidazolium Bromide is not only reliability on the balance, but performance in the hands of the chemists and engineers who trust it. As the chemistry world moves forward, we work to stay a step ahead—focusing on product improvements that matter where it counts: in the outcomes and the ease of working with a partner who builds from scratch, not from speculation.