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HS Code |
492113 |
| Chemical Name | 1-Butyl-2,3-Dimethylimidazolium Toluenesulfonate |
| Cas Number | 824456-19-7 |
| Molecular Formula | C15H24N2O3S |
| Molecular Weight | 312.43 g/mol |
| Appearance | White to off-white solid |
| Solubility In Water | Soluble |
| Density | 1.15-1.20 g/cm³ (approximate) |
| Boiling Point | Decomposes before boiling |
| Purity | Typically ≥98% |
| Storage Conditions | Store in cool, dry place, tightly sealed |
| Synonyms | [BM2MI][OTs]; 1-Butyl-2,3-dimethylimidazolium p-toluenesulfonate |
| Ionic Liquid | Yes |
| Odor | Odorless |
| Stability | Stable under recommended storage conditions |
As an accredited 1-Butyl-2,3-Dimethylimidazolium Toluenesulfonate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 500g of 1-Butyl-2,3-Dimethylimidazolium Toluenesulfonate, sealed in an amber glass bottle with a secure screw cap and chemical label. |
| Shipping | **Shipping Description:** 1-Butyl-2,3-dimethylimidazolium toluenesulfonate is shipped in tightly sealed containers, protected from moisture and direct sunlight. Handle with appropriate personal protective equipment. Store at ambient temperature. Follow all local, national, and international regulations for transport. Ensure packaging is secure to prevent leaks or spills during transit. Not classified as hazardous for transport. |
| Storage | 1-Butyl-2,3-dimethylimidazolium toluenesulfonate 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 the container away from direct sunlight and sources of ignition. Proper labeling and secondary containment are recommended to prevent leaks or accidental exposure. Use appropriate personal protective equipment during handling. |
Applications of 1-Butyl-2,3-Dimethylimidazolium Toluenesulfonate in Industrial ManufacturingOur factory supplies 1-Butyl-2,3-Dimethylimidazolium Toluenesulfonate directly to advanced industrial users for specialty synthesis, complex separations, electrochemical devices, and related downstream technical sectors. Below, we detail the material’s established applications in core downstream segments where this ionic liquid proves essential because of its unique physicochemical profile. 1. Catalyst and Reaction Medium for Selective Organic SynthesisChemical manufacturing plants utilize this ionic liquid as both a green solvent and a phase-transfer catalyst, especially in alkylation, acylation, and cycloaddition reactions. The unique ionic environment enables high selectivity and repeatable yields for intermediates such as functionalized aromatics and heterocycles. Staff control dosing carefully to optimize conversion rates without promoting side reactions or undesired by-products. Industry compliance standards
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2. Electrolyte Additive for Supercapacitors and High-Performance BatteriesManufacturers of electrical energy storage devices incorporate this ionic liquid into composite electrolytes to increase operating voltage windows and suppress electrolyte volatility. Its non-flammable nature and wide electrochemical stability range support safer and more durable device architectures, particularly for large-format or automotive-grade modules. Industry compliance standards
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3. Extractive Solvent for Aromatic Hydrocarbon SeparationPetrochemical operators deploy this ionic liquid in aromatics extraction units due to its high selectivity for benzene, toluene, and xylene recovery from reformate streams. This application improves yield purity for petrochemical feedstocks and enables energy savings compared to traditional sulfolane or glycol processes, especially under variable feed conditions. Industry compliance standards
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4. Solubilizing Agent and Reaction Host in Cellulose Dissolution for Advanced MaterialsFacilities engaged in the direct dissolution and regeneration of cellulose exploit this ionic liquid for dissolving wood pulp and plant-derived fibers, bypassing traditional viscose or copper-ammonia systems. The material’s ability to disrupt and solubilize hydrogen-bonded polymer networks enables preparation of transparent films, microfibers, and specialty hydrogels for medical and filtration end uses. Industry compliance standards
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5. Homogeneous Medium for Metal Complex Catalyzed CO2 ConversionResearch-scale and pilot facilities working on CO2 utilization introduce this ionic liquid as a polar, thermally stable solvent system for metal-catalyzed conversion of carbon dioxide into cyclic carbonates or methanol derivatives. Its high CO2 solubility and capacity to stabilize transition metal complexes accelerate key steps under moderate temperature and pressure conditions. Industry compliance standards
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Producing 1-butyl-2,3-dimethylimidazolium toluenesulfonate in-house has taught us the practical value of controlled synthesis and attention to detail. In the lab, the formation of this ionic liquid doesn’t leave much room for shortcuts. Each batch requires balancing butyl, methyl, imidazolium, and toluenesulfonate—one overlooked detail can lead to inconsistency or contamination. Over years of hands-on work, we’ve honed our process, so our product meets the standards demanded by researchers and chemical manufacturers seeking more predictable results.
Countless conversations with formulators and scale-up teams highlight the challenges around traditional solvents and older-generation ionic liquids. In many situations, legacy materials fall short under heat, struggle with catalysis, or yield inconsistent reaction profiles. With 1-butyl-2,3-dimethylimidazolium toluenesulfonate, we help customers move past these roadblocks. The unique cation structure and sulfonate anion come together in a compound that widens operational options on the bench and in the plant.
For those working on metal-catalysis, stubborn organic transformations, or advanced separation techniques, the choice of medium matters just as much as any catalyst. This ionic liquid not only dissolves a remarkable range of substrates, it holds up during repeated cycles and extreme conditions. We have run round after round of recycling tests, and the stability impressed our own technical teams—minimal loss of performance after more than a dozen cycles is the rule, not the exception.
In our production experience, clarity about specifications—purity, moisture, color, and residual contaminants—matters more than list-form data sheets can convey. For this compound, we keep water and halides low, typically below 500 ppm. Customers say the absence of base halides leads to fewer side products and cleaner extractions. The slightly viscous, pale-yellow liquid pours with little odor if handled correctly. Each batch runs through NMR, GC-MS, and sometimes elemental analysis, not as a box-check but to ensure the material meets actual working needs—if you care about catalysis or advanced material synthesis, you’ll notice the difference.
Every order leaves us with a tightly specified product, directly traceable to the batch and operator. Our team stands behind the actual certificate, so if unexpected performance issues crop up in your lab, it’s not brushed off—we’ve taken calls from customers in the middle of overnight runs, and we track and resolve any issue. Working directly with us, end-users cut through the noise of “generic” product and get direct access to the people who made the compound, whether they’re optimizing a novel synthetic pathway or scaling for a new commercial application.
After working with dozens of ionic liquids over the years, we recognize how design tweaks change behavior. Adding methyl groups at both the 2 and 3 positions on imidazolium boosts thermal stability and shields the backbone from nucleophilic attack. These aren’t armchair modifications; they make a measurable difference in both shelf life and cycle life. The butyl sidechain gives just enough flexibility for handling, without introducing heavy aromatic character or excessive viscosity, so dosing and mixing become hassle-free. With a lab full of candidates, we consistently choose 1-butyl-2,3-dimethylimidazolium toluenesulfonate for its well-rounded performance in tasks where lesser ionic liquids can’t take the heat or fall apart under stress.
We’ve supplied this compound to teams investigating biomass conversion, pharmaceutical intermediate synthesis, and rare earth extractions. In real workflows, its strong solubilizing power opens doors for non-traditional substrates or previously intractable reaction partners. For catalysis, its non-coordinating toluenesulfonate anion brings good conductivity but won’t poison sensitive catalysts, as we’ve seen in gold- and palladium-catalyzed processes. In separation science, researchers who previously found extensive extractant loss now praise its low volatility and ease of recovery.
We work closely with membrane developers using this ionic liquid as a dopant or charge carrier. Each time, they return to the same point—standard solvents or single-methyl imidazolium salts can’t compete with the durability, ease of handling, and predictable ionic environment. These characteristics help avoid costly setbacks in pilot plants or multi-step syntheses. Teams tell us they used to see fouling or inconsistent transport across their membranes, but with our product, operation smooths out and they get the reproducibility they need.
Anyone who works closely with ionic liquids knows their safe handling calls for respect, not just rote compliance. We emphasize proper ventilation and storage, not just because of best-practice requirements, but because we’ve dealt with outlier cases—polymerization under heat, rare degradation when exposed to strong bases, odd reactions with careless handling. Experience means learning from such events and building smarter process steps: onboard drying tubes, inert atmosphere for long-term storage, or slow addition protocols for exothermic reactions.
We always urge customers to start small and scale up only after evaluating compatibility and safety in their own setting. Taking these steps isn’t about ticking off a checklist; it’s about problem avoidance and building up reliability over the long run. When you know the history of a product from the hands that produced it, it’s easier to trust—and safer, too—than picking from an anonymous catalog.
The learning never stops at the production level. Over the past decade, chemists worldwide have shared practical concerns—batch-to-batch color variance, slow pourability in cold weather, tiny differences in conductivity affecting sensor calibration. Some of these insights have pushed us to look deeper at upstream processing, from raw material qualification to reactor temperature control. We established in-process controls and supply chain audits, not on paper, but so the next customer gets what their research or process expects, period.
Collaborating directly with users has changed how we approach synthesis. Early on, we realized water content was more than a specification—too much, and catalytic cycles get thrown off or active sites deactivate. We upgraded our in-line drying system and started providing test data right with the delivery. Over time, as we saw more catalytic uses, we became meticulous about limiting halide carry-over. That matters especially in ligand-sensitive environments and helps our customers claim better yields or longer catalyst life, a fact several shared at recent industry workshops.
A few years ago, we often supplied traditional alkyl-imidazolium salts and other ionic liquids with different anions. These saw plenty of use, but regulars reported similar drawbacks: higher volatility, unpredictable viscosity shifts, halide interference, or toxic byproducts. As regulations in green chemistry and manufacturing have grown tougher, more customers began searching for ionic liquids that simplify compliance while maintaining operational benefit.
Our product helps address these shifting needs. Unlike more volatile ammonium- or phosphonium-based materials, 1-butyl-2,3-dimethylimidazolium toluenesulfonate generates almost no measurable vapor at standard process temperatures. Spills and process losses drop, and exposure risks for crew decrease. Its methylated backbone makes it less prone to hydrogen abstraction or nucleophilic mischief. Over dozens of trial reports, this means fewer workups and cleaner product collection—attributes that have won us repeat business and long-term partnerships.
Supply reliability never comes by accident. Our direct oversight removes the layers of confusion that come with trading intermediaries. We purchase and test each input ourselves, clean the vessels between production runs, and keep manufactured inventory on site so orders ship without delay. On more than one occasion, we’ve fielded urgent requests from research programs or plant launches delayed by short supply elsewhere, moving quickly to deliver with the documentation needed for approval processes.
We know the details behind sourcing—some batches of raw imidazole precursors can change the color or odor profile, or contain difficult-to-detect trace metals that influence process chemistry downstream. Our team runs advanced analytical checks, not because a customer requested it, but because a single out-of-spec batch can set back ongoing research or lead to months of troubleshooting in a commercial setup. By caring about these details, we build the kind of trust that only grows from long-term collaboration and honest communication.
One industrial partner came to us after repeated catalyst failures in a pilot plant focused on C-C coupling reactions. Their previous solvent, a standard imidazolium bromide, reacted unpredictably with some organometallic intermediates. We reviewed their process and supplied 1-butyl-2,3-dimethylimidazolium toluenesulfonate. Cycle after cycle, their yield climbed, waste dropped, and they no longer needed as much post-run purification. A second customer in materials R&D reported trouble with membrane consistency, blaming swelling and collapse during thermal cycling. Testing with our compound validated that its stability and low water uptake made the difference—device performance metrics finally matched the simulation results, unlocking scale-up funding.
Academic labs investigating organic electrosynthesis often seek out unique ionic environments for precise control over ion transport and intermediate speciation. Our product’s sulfonate anion and methylated imidazolium core let them avoid competitive coordination and reach higher current densities with less degradation. It isn’t just a matter of substitution—it’s about solving specific limitations in established protocols, so discovery proceeds confidently.
In the ongoing shift toward sustainable chemistry, manufacturing choices make a real impact. Regulators and stakeholders want substances that reduce risk, environmental impact, and operator exposure. Over the last few years, we’ve seen stronger demand for non-volatile, thermally-robust solutions that replace hazardous solvents and minimize post-reaction scrubbing. Our ionic liquid fits these needs without forcing radical flowchart changes, making compliance and process improvements more achievable.
More research groups and pilot plants now use our product as the enabling medium for CO2 capture, lignocellulosic biomass pretreatment, and high-efficiency separations. Matching a cleaner process with predictable recycling means teams save money, training time, and avoid regulatory headaches. By supporting these transitions with consistent supply, batch documentation, and on-call technical support, we help our customers move their green chemistry ambitions from the lab to the commercial floor.
Manufacturing 1-butyl-2,3-dimethylimidazolium toluenesulfonate isn’t abstract theory for us—it’s a series of technical choices, problem-solving moments, and commitment to continuous learning. As the needs of chemical researchers and industrial teams evolve, so too do our processes and attention to detail. Customers have come to trust the hands-on experience behind every batch, not just for performance metrics, but for the transparency and communication that help resolve new challenges as they emerge.
If your application calls for stability, low volatility, excellent solvation, and cation/anion profiles engineered for modern chemistry, this compound is worth considering. You’ll talk to the chemists who made your material, not an anonymous voice somewhere in a distribution chain. With years of practical feedback and supply chain control, we push to deliver results—so your research, development, or production can push forward, too.