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1-Benzyl-3-Methylimidazolium Tosylate

    • Product Name 1-Benzyl-3-Methylimidazolium Tosylate
    • Alias [Bmim][OTs]
    • Einecs 629-688-5
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    640634

    Product Name 1-Benzyl-3-Methylimidazolium Tosylate
    Chemical Formula C17H20N2O3S
    Molecular Weight 348.42 g/mol
    Appearance White to off-white solid
    Melting Point 102-106 °C
    Solubility In Water Soluble
    Density 1.21 g/cm3
    Purity Typically >98%
    Cas Number 336481-97-3
    Storage Temperature Room temperature (RT)
    Boiling Point Decomposes before boiling
    Function Ionic liquid

    As an accredited 1-Benzyl-3-Methylimidazolium Tosylate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 100g package features a sealed amber glass bottle labeled “1-Benzyl-3-Methylimidazolium Tosylate,” with hazard warnings and batch details.
    Shipping 1-Benzyl-3-Methylimidazolium Tosylate is shipped in tightly sealed containers to prevent contamination and moisture exposure. The chemical should be handled with care and transported according to regulations for non-hazardous, laboratory-grade chemicals. Proper labeling and documentation are included, ensuring safe delivery and compliance with relevant shipping and safety standards.
    Storage Store 1-Benzyl-3-Methylimidazolium Tosylate in a tightly sealed container, protected from moisture and light. Keep in a cool, dry, and well-ventilated area away from incompatible substances such as strong oxidizers. Ensure the storage area is clearly labeled and complies with local chemical safety regulations. Use appropriate personal protective equipment when handling to avoid skin and eye contact.
    Application of 1-Benzyl-3-Methylimidazolium Tosylate

    Applications of 1-Benzyl-3-Methylimidazolium Tosylate in Industrial Manufacturing

    As a manufacturer of specialty ionic liquids, we supply 1-Benzyl-3-Methylimidazolium Tosylate for advanced industrial applications across selective sectors. This material enables innovative processing, enhanced selectivity, and environmental benefits within complex production environments. Below, we detail specific segment uses, compliance demands, dosing approaches, process stages, and the types of value-added end products our customers manufacture.

    1. Catalytic Solvent in Cross-Coupling Pharmaceutical Synthesis

    Researchers and pharmaceutical API production teams adopt this ionic liquid as a polar, non-volatile reaction medium for palladium-catalyzed cross-coupling synthesis. Its strong solvation properties enhance catalyst turnover, especially for C–N and C–C bond formation in heterocycle drug intermediates. Texture, color, and yield consistency hinge on careful process control in pilot and large-scale reactors, benefitting from minimized VOC emissions and easier downstream separation. Purity profiles meet stringent QC demands for active pharmaceutical ingredients.

    Industry compliance standards

    • ICH Q7 GMP for active pharmaceutical ingredient manufacture
    • EU GMP EudraLex Volume 4
    • FDA 21 CFR Part 211
    • Ph. Eur. general monographs (for residual solvents and purity)

    Typical usage ratio

    • 10–30% v/v as primary solvent system or co-solvent; adjusted by substrate solubility, targeted impurity removal, and reaction kinetics

    Downstream process integration

    • Material addition during coupling, amidation, or alkylation steps; recycled or removed post-reaction by aqueous extraction or antisolvent precipitation

    Final product types

    • Pyrimidine and indole derivatives
    • Active pharmaceutical intermediates (APIs)
    • Specialty chloroanilines and heterocyclic drug building blocks
    • Final formulated APIs after purification

    2. Electrolyte Additive for Electrochemical Sensor Manufacturing

    Manufacturers of electrochemical sensors incorporate this ionic liquid in the formulation of advanced polymer gel electrolytes. Its high ionic mobility, chemical inertness, and wide electrochemical window increase device stability and enable miniaturized sensor architecture. High-purity product helps reduce signal drift and cross-contamination during continuous manufacturing or inkjet-based micro-patterning. Consistent batch-to-batch quality supports rigorous performance validation.

    Industry compliance standards

    • IEC 60747-5-5 (electronic devices)
    • ISO 13485:2016 (Medical Devices QM)
    • REACH (for handling ionic liquids in the EU)
    • RoHS Directive (2011/65/EU)

    Typical usage ratio

    • 2–8% w/w of total polymer electrolyte composition; increased for enhanced ionic conductivity or reduced for viscosity adjustment

    Downstream process integration

    • Pre-mixing into polymer dispersions prior to coating or casting onto sensor substrates; utilized in roll-to-roll or batch sensor chip production lines

    Final product types

    • Hydrogen and ammonia gas sensors
    • Glucose oxidase-based biosensors
    • Wearable chemical monitoring patches
    • Disposable diagnostic test strips

    3. Cellulose Dissolution Solvent in Bio-based Fiber Spinning

    Producers of regenerated cellulose fibers use our ionic liquid in wet spinning of viscose alternatives. Its strong hydrogen-bond disruption allows rapid dissolution of various lignocellulosic biomass without xanthation or toxic carbon disulfide. Fiber properties, including tenacity and uniformity, depend on solvent consistency and impurity profile. Process optimization reduces need for multi-step purification and limits environmental waste.

    Industry compliance standards

    • OEKO-TEX® Standard 100 (fiber safety)
    • ISO 9001 (QMS for textile raw materials)
    • ZDHC Manufacturing Restricted Substances List (version 3.1, for solvent management)
    • EU REACH Annex XIV compliance

    Typical usage ratio

    • 55–80% w/w in cellulose solution formulations; regulated by cellulose grade, fiber spinning speed, and viscosity targets

    Downstream process integration

    • Direct addition to dissolvers with milled pulp; utilized until gelation point before extrusion through spinnerets; recovery by anti-solvent bath and post-filtration

    Final product types

    • Lyocell continuous filament
    • Bicomponent eco-fibers for nonwovens
    • High-strength industrial yarns
    • Textile-grade spun cellulose for apparel

    4. Organometallic Catalyst Stabilizer in OLED Material Synthesis

    Chemical suppliers for the OLED and advanced material industry apply this ionic liquid in the ligation and stabilization of transition metal complexes for blue and green emissive layers. Enhanced catalyst life and reproducibility improve yields of metal-organic compounds with demanding photophysical properties. Sourcing high-purity batches reduces risk of introduced halides or protic contaminants, maintaining PLQY (photoluminescence quantum yield) within target ranges.

    Industry compliance standards

    • ISO 9001 (QMS for fine chemical synthesis)
    • IEC 62341 (OLED display requirements)
    • Cleanroom ISO Class 5–7 standards (for display industry)
    • REACH Substances of Very High Concern (SVHC) exclusion

    Typical usage ratio

    • 0.5–3.0 mol% relative to metal precursor; level refined by catalyst activity, ligand-to-metal ratio, and synthesis temperature

    Downstream process integration

    • Charged during metal precursor complexation; solubilizes organic ligands and metal salts in hot-stage reactors or glovebox environments

    Final product types

    • Blue iridium phosphorescent dopants
    • Cyclometalated platinum complexes for OLED
    • OLED emitter ink formulations
    • High-purity evaporation grade OLED precursors
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    Certification & Compliance
    More Introduction

    Introducing 1-Benzyl-3-Methylimidazolium Tosylate: Practical Insights for Industrial Users

    Our Commitment to Consistency in 1-Benzyl-3-Methylimidazolium Tosylate Production

    Every manufacturer faces unique challenges when bringing a new ionic liquid to the market, especially one like 1-Benzyl-3-Methylimidazolium Tosylate. For years, we have focused on building a process that delivers a reliable product batch after batch, because our clients count on precise performance. Over time, much of our core know-how has come from testing, troubleshooting, and customizing each production run to keep both product composition and quality precisely in line with expectations.

    When we first started producing 1-Benzyl-3-Methylimidazolium Tosylate, several key learning curves defined the way we do things today. Unlike more commonly seen imidazolium salts, small process shifts often led to significant changes in product purity or crystal habit. During the early days, minor batch variations tended to affect conductivity, melting point, or solubility. We countered these problems by refining both feed control and purification methods, so the final ionic liquid stays consistent in composition—from the start of the barrel to the last drum.

    1-Benzyl-3-Methylimidazolium Tosylate has proved especially attractive for chemists who want a non-volatile, thermally stable ionic solvent, but who also want the specific interaction capabilities conferred by the benzyl group and tosylate counterion. Our onsite feedback loop, which starts at raw material qualification and runs through QA batch analysis, has shown us just how important each step is. Even a small difference in methylimidazole input or benzyl chloride supply changes not only yields, but can alter physical properties later on. That’s the sort of detail manufacturers see daily, and it’s one of the biggest reasons customers connect with the product once they see its advantages in the lab or on the factory floor.

    How We Approach Specifications and Quality in Production

    For end users, the technical specification defines clear expectations. Over the past decade, our 1-Benzyl-3-Methylimidazolium Tosylate has been supplied as a white to off-white crystalline solid—each lot checked by melting point, NMR, and water content analyses, using routine Karl Fischer titration to keep moisture below permitted limits. The expected melting range usually sits near 85-90 °C on a properly controlled run, which lines up with most published benchmarks in international literature.

    Key purity checks include limiting halide residuals, ensuring complete reaction of benzyl chloride, and confirming correct counterion identity by FTIR and titration. We have observed that any deviation in counterion content—such as incomplete tosylation—leads to noticeable differences in downstream application performance, whether as an organocatalyst phase or in extraction. That triggers not only batch rejection on our end, but a full root-cause review. With hands-on experience, chemists and operators learn to anticipate and head off many problems before they ever reach the QA lab.

    Some products offer a narrow margin for error, and 1-Benzyl-3-Methylimidazolium Tosylate is one of them. The benzyl group adds to the bulk and hydrophobicity of the cation, tweaking solubility and physical behavior compared to smaller imidazolium salts. If the starting materials supply drifts in quality—even by a small margin—the effects show up quickly, whether as off-spec melting points or as drops in batch yield. In response, we adjusted our inventory control and supplier auditing, running additional identity and purity checks on all incoming key reagents. These tight quality checks mean less risk for users who depend on predictability in their solvent systems or separation columns.

    Application Experience: Where 1-Benzyl-3-Methylimidazolium Tosylate Delivers Value

    Our primary customers work in advanced synthesis, analytical separations, and sometimes polymer processing. Early on, academic interest in this compound focused on its abilities as a chlorinating agent carrier or as an electrolyte in non-aqueous media. The addition of the benzyl group produces an ionic liquid that is not only less volatile than common imidazolium salts, but which exhibits improved ability to dissolve aromatic compounds and certain transition metal complexes. Over the years, much of the positive feedback we’ve received stems from these selectivity gains, especially in reactions or processes involving aromatic substrates.

    End users who have switched from smaller straight-chain imidazolium derivatives (like 1-butyl-3-methylimidazolium) comment that the benzyl group changes materials compatibility in a favorable way. Practical tests in nucleophilic substitution reactions and ionic liquid-based phase separations have returned notably higher yields, often attributed to improved miscibility. We learned from customer returns and field support that immediate filterability and easier solvent exchange also improve, leading to less downtime during scale-up campaigns. These aren’t theoretical advantages—they save labor and reduce cost per batch. Like most things in chemical manufacturing, value shows up at the most practical moments: shorter downtime, easier phase separation, and actual higher purity in isolated products.

    Chemists using our product in electrochemical applications note a unique set of properties, including low vapor pressure, wide electrochemical window, and inertness toward many classes of functional groups. These qualities matter for researchers looking to develop batteries or double-layer capacitors using safer and more tunable electrolytes. Our hands-on support has created opportunities for process engineers to trial customized variants as well, supporting research into higher capacity cells or new redox chemistries. Long-term, production partnerships often grow from these sorts of early trial collaborations.

    Comparing to Other Ionic Liquids: Differences and Performance Implications

    Compared to traditional imidazolium ionic liquids that use smaller cations like methyl or butyl, 1-Benzyl-3-Methylimidazolium Tosylate offers distinct handling and performance traits. In production, the presence of the benzyl ring slightly elevates melting point and increases viscosity, making physical transfer and mixing a bit more demanding but also enabling more robust thermal cycling. Since the tosylate anion has moderate hydrophilicity and reduced nucleophilicity compared to halide or tetrafluoroborate, we see less potential for corrosive side reactions in many settings. Lab techs who need to avoid unsafe byproducts often request this combination.

    Over repeated production runs, we have seen that this product resists hydrolysis better than similar compounds using less stable anions, keeping shelf life longer and producing less hydrolytic breakdown during storage conditions. This has become a real advantage for users working in environments where batch storage flexibility is a daily concern. Handling properties also matter. Benzyl-functionalized imidazolium products tend to be less prone to odorous decomposition than their methylated or butylated relatives—a fact we’ve confirmed both in daily site experience and in controlled stability studies. That means operators spend less time dealing with minor spills or cleaning up residual vapors, especially in warm conditions.

    Selection of this material over other ionic liquids typically reflects a demand for higher selectivity or improved compatibility with aromatic organics, along with greater stability in reactions involving strong nucleophiles. Feedback from our application partners has shown this product survives harsher environments and repeated recycling with negligible loss in yield or purity, as long as storage conditions stay dry and sealed.

    Process Learning: How Our Manufacturing Practice Shapes Product Consistency

    Producing a stable batch of 1-Benzyl-3-Methylimidazolium Tosylate requires attention to nuance at each step. For instance, benzyl chloride feedstock quality plays a central role in final product purity. If trace water enters the system or if reagent charge ratios slip, off-target impurities such as unreacted starting material or byproducts like dibenzylimidazolium can emerge, which creates a real problem in critical applications. Our operators use active moisture monitoring and pre-drying of glassware and reactors to minimize this risk, having learned the hard way that certain contaminants resist post-synthesis removal.

    Crystal habit and filtration speeds also change with minor batch variations. We’ve recognized certain cooling profiles in crystallization yield better filter cake formation, leading to easier downstream washing. Operators train new staff on these subtle process signatures, ensuring they recognize sticky or slow-filtering lots and can proactively adjust filtration speed or solvent washes to improve outcomes. Site-level knowledge can cut hours off the processing time for each ton of material, reducing both costs and operational backlogs.

    Every production run includes full identity checks (NMR, FTIR, elemental analysis) before release, as we have learned that even visually perfect crystals may contain invisible shortfalls in anion-to-cation ratio or trace solvent retention. In the rare event of an off-spec batch, rather than relying only on automated log files, we task a crew to dissect the process notes, bringing insights from every level of the operation into the review. This approach has helped raise our plant’s average approval rate and directly benefits the R&D shift teams developing process improvements.

    Practical Application Scenarios: What Real World Users Have Achieved

    Users in research and industrial labs have driven most application insights. In catalytic reactions, researchers reported higher selectivity or output yields when using our material as the ionic phase, largely due to improved interaction with organometallic catalysts and stabilized transition states. A large-scale batch user in extraction chemistry confirmed that using this ionic liquid reduced their workload on downstream purification, freeing up resources for further development.

    Another interesting example comes from the field of polymer dissolution and reformation. 1-Benzyl-3-Methylimidazolium Tosylate, with its bulkier cation, offers just enough steric hindrance to facilitate dissolution of cellulose derivatives, while remaining easy to remove from finished materials. These differences translate into practical execution advantages: reduced need for post-synthesis wash cycles, and lower solvent recovery input, each time. In situations where environmental compliance requires minimizing waste, these efficiencies count.

    Operators in analytical chemistry find this material performs especially well as a phase transfer catalyst or as a stationary phase in chromatographic separations where the goal is to resolve aromatic analytes from complex mixtures. Its unique solvation profile lets users fine-tune method development, adjusting retention and elution curves with more precision. One customer using our product in a sequence of gas-solid reactions found the predictable retention time repeatability translated into faster sample processing across dozens of runs.

    On the Front Line: Production Safety, Handling and Warehousing

    From a plant operations point of view, safe handling and efficient storage play almost as large a role as synthesis technique. Our teams rely on careful drum management and labeling, supported by solid batch tracking so every container’s origin is unmistakable. Most of our product is shipped in sealed, moisture-protected drums with internal liners, eliminating exposure to humidity during inland transit.

    We have learned that temperature swings affect not just storage stability but also transfer and weighing. At temperatures above the melting range, viscosity decreases quickly and handling becomes more straightforward; when kept close to room temperature, material may require gentle warming to ensure complete transfer. Site training reinforces the importance of carefully staged warming—never direct heating—since hot spots will degrade material at points of contact. This simple operational lesson has helped minimize internal loss and material darkening over time.

    Safety protocols remain matched to hands-on experience. Although the product’s low volatility and minimal odor risk make it less hazardous to handle than many raw reactants, best practice includes the use of splash goggles and gloves. Our line operators treat each production run as a chance to reinforce habits that maintain batch integrity and reduce cross contamination. Spills rarely occur, but staff are drilled on immediate cleanup and neutralization steps, knowing that even minor residue can affect both QC analyses and subsequent batch composition.

    Raw Material Sourcing and Supply Chain Security

    No chemical operation runs smoothly without secure supply chains. Our plant’s procurement team spends considerable time qualifying, auditing, and maintaining stable sources for key input materials. Both benzyl chloride and methylimidazole—critical inputs for our process—come from long-standing, traceable suppliers whose quality records have been proven over many years. During world events that created shipping delays or raw material price spikes, our forward contracting and inventory planning enabled uninterrupted customer supply.

    We also invest in second-source qualification, allowing for transition to backup suppliers without losing batch control. Incoming goods inspection, from identity checks to moisture and purity testing, helps us avoid downstream surprises. Plant operators have shared real stories of the challenges that arise from even seemingly minor upstream changes; one memorable episode occurred when a benzyl chloride lot arrived with slightly elevated stabilizer content, which required an immediate reconsideration of reaction sequence to keep by-product formation within specs. Experience like this underlines the importance of experienced staff and robust tracking at every stage.

    Users regularly approach us for collaboration around custom synthesis and for troubleshooting unusual supply needs. In these circumstances, we review client requirements in the context of both immediate factory capability and longer-term process adaptability. The flexibility to respond to changing market and research needs only comes from hard experience running these processes day in and day out.

    Environmental Considerations and Responsible Disposal

    Environmental impact remains a vital concern for our operation and our customers. Ionic liquids like 1-Benzyl-3-Methylimidazolium Tosylate deliver reduced volatility and generally low eco-toxicity in comparison to traditional organic solvents, but responsible stewardship extends beyond product selection. We routinely work with downstream users to ensure compliance with local waste laws and best practices for treatment or recycling.

    Our own facility employs closed-loop wash and recovery steps, keeping emissions, water discharge, and solid byproduct generation to a minimum. Investment in better solvent recovery has paid off both in reduced environmental burden and in raw material cost savings—advantages we pass on to customers. Where possible, we seek out partners who are willing to participate in product take-back or in pilot recycling initiatives. Some users have already joined early trials focused on secondary purification and re-use of spent ionic liquids. Our operations teams record each of these efforts, building towards better global sustainability metrics.

    Supporting Innovation in Applied Chemistry: Our Outlook

    Producers rarely operate in isolation from end users. A significant part of our routine centers on open lines of communication, whether that’s new requests, troubleshooting, or building a collaborative process improvement framework. Our team has grown not only by delivering stable lots of 1-Benzyl-3-Methylimidazolium Tosylate, but by integrating feedback from chemists, process engineers, and supply chain partners around the world.

    The demand for next-generation ionic liquids with tailored performance traits runs high. Our own work in this space spans not just this compound, but a family of functionalized imidazolium salts and other onium derivatives, each launched in response to a specific technical challenge relayed by a customer. The journey from pilot batch to commercial run takes patient teamwork—especially when organizations are sharing both victories and hard lessons. Only by listening carefully and responding directly can we hope to keep pace with evolving industry needs and safety regulations.

    With each year, new opportunities for 1-Benzyl-3-Methylimidazolium Tosylate emerge, pushing us toward ever greater rigor in our manufacturing and application know-how. The bridge between plant floor and practical end use stays strong through daily experience, clear feedback, and the shared drive to improve chemical solutions for the next set of challenges.