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HS Code |
169366 |
| Chemical Name | 1-Tetradecyl-3-Methylimidazolium Bromide |
| Cas Number | 463189-22-6 |
| Molecular Formula | C18H35BrN2 |
| Molecular Weight | 359.39 g/mol |
| Appearance | White to off-white powder |
| Melting Point | 90-100 °C |
| Solubility In Water | Soluble |
| Purity | Typically ≥98% |
| Storage Temperature | Room temperature (protected from moisture) |
| Density | 1.034 g/cm³ |
| Ionic Liquid Class | Imidazolium-based |
| Synonyms | [C14mim]Br |
As an accredited 1-Tetradecyl-3-Methylimidazolium Bromide factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle, 25g, tightly sealed with a screw cap, labeled with hazard warnings and product details in bold black text. |
| Shipping | Shipping for 1-Tetradecyl-3-Methylimidazolium Bromide is handled with care, using airtight, sealed containers to prevent moisture exposure. Packages are clearly labeled as chemicals and comply with relevant regulations. The product is typically shipped via ground or air transport, depending on destination, with safety data sheets included for proper handling information. |
| Storage | Store **1-Tetradecyl-3-Methylimidazolium Bromide** in a cool, dry, well-ventilated area away from direct sunlight and sources of ignition. Keep the container tightly closed and protected from moisture. Store away from incompatible substances such as strong oxidizers and acids. Use appropriate secondary containment and clearly label the storage area. Handle with proper personal protective equipment to prevent contamination. |
Applications of 1-Tetradecyl-3-Methylimidazolium Bromide in Industrial ManufacturingAs the direct producer of 1-Tetradecyl-3-Methylimidazolium Bromide, we deliver this ionic liquid to diverse industrial sectors, supporting both established and advanced chemical process demands. Below are verified downstream applications based on industrial formulation experience and customer integration feedback. 1. Surfactant and Emulsifier in Pharmaceutical Intermediate SynthesisPharmaceutical manufacturers rely on our ionic liquid as a phase-transfer catalyst and emulsifier to boost yield in multi-phase reactions for high-purity intermediate synthesis. Its long alkyl side chain supports improved miscibility between organic and aqueous phases, especially in selective alkylation and nucleophilic substitution processes. Operators typically pre-mix the compound with reactants, adjusting the loading as per batch scale and sensitivity of the target compound. Industry compliance standards
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2. Antistatic Agent in Polyolefin and Engineering Polymer CompoundingOur 1-Tetradecyl-3-Methylimidazolium Bromide serves as an organic cationic antistatic additive for the plastics industry. Compounders introduce this material during extrusion or masterbatch processing to lower surface resistivity in polyolefins and polyamides. It supports stable static dissipation for downstream electronic packaging, cleanroom components, and automotive interior parts. Industry compliance standards
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3. Electrolyte Component for Advanced Energy Storage DevicesBattery and supercapacitor makers incorporate this material as an ionic liquid electrolyte or electrolyte additive, leveraging its high thermal stability and wide electrochemical window. The compound boosts charge transport and supports improved cycle life in lithium-ion and hybrid capacitors. Manufacturers manage precise blending under inert atmospheres to meet electrolyte conductivity and voltage demands. Industry compliance standards
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4. Corrosion Inhibitor in Oilfield and Downhole Chemical SystemsOilfield service operators use our proprietary ionic liquid structure as a cationic corrosion inhibitor deployed in acidizing and enhanced oil recovery processes. Its amphiphilic balance enables strong adsorption onto steel surfaces, effectively reducing corrosion rates in pipelines, downhole tubulars, and production circuits exposed to brine and hydrogen sulfide. The material is supplied as a liquid additive, compatible with high-salinity and broad pH fluids. Industry compliance standards
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5. Fabric Softener and Antimicrobial for Specialty Textile FinishingFinishing chemicals specialists incorporate this raw material as a cationic softener and antimicrobial agent in high-performance textile treatment. The imidazolium ionic head achieves deep interaction with fiber surfaces, facilitating lasting softness and odor protection, especially on polyester, cotton, and microfiber blends. Textile processors apply the material post-dyeing using exhaust or padding methods under controlled temperature and pH. Industry compliance standards
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In the world of fine chemicals, 1-Tetradecyl-3-methylimidazolium bromide stands out for several compelling reasons. We've spent years refining the process to produce this ionic liquid consistently, monitoring every batch as closely as any craftsman follows a beloved recipe. From the start, our goal has been simple: deliver reliable, high-performing chemistry to research labs and specialty industries, without fluff or compromise.
Chemists searching for task-specific ionic liquids quickly notice the unique balance 1-Tetradecyl-3-methylimidazolium bromide brings to the table. With a C14 alkyl chain on the imidazolium ring, this compound offers surface-active properties not typically seen in its shorter-chain analogues. From a manufacturing perspective, maintaining purity during the alkylation and quaternization steps becomes critical; side reactions, trace water, and residual starting materials must be controlled tightly. Our facility’s approach hinges on meticulous control, achieved through in-line monitoring, stainless transfer lines, and high vacuum drying.
Imidazolium-based ionic liquids have earned their place in research, but few deliver the amphiphilic balance seen here. The tetradecyl group imparts remarkable solubility in organic and some aqueous phases, opening the door for applications in phase transfer catalysis, micellar chemistry, and nano-material synthesis. Unlike short-chain homologues, the longer chain in this compound drives the formation of well-defined micelles and even liquid crystalline phases at room temperature. This property is not an abstract advantage – researchers working on self-assembly, or formulating safer solvent systems, find this structure pivotal for controlling aggregation and molecular orientation.
Producing a high purity product, especially at the tail end of a long carbon chain, often creates hurdles. We’ve seen how minor impurities—especially chain-shortened or bromide-insufficient fractions—cause erratic behavior when customers run NMR, IR, or even test performance in catalysis. Ongoing investments in analytical quality control, including high-resolution mass spectrometry and quantitative Karl Fischer titration for water content, keep us confident batch after batch. Our QC teams often return to the reactor floor for root-cause investigations, knowing that even “minor” contaminants can derail sensitive research.
Some customers ask if there’s a real difference between tetradecyl and other alkyl chain imidazoliums. From our direct trial-and-error experience, the answer is clear. In solution, this compound’s balance of hydrophobicity and ionic character enables more robust emulsification properties and lower critical micelle concentrations (CMC) than similar options. For dispersing carbon nanotubes, stabilizing nanoparticles, or extracting precious metals from spent catalysts, this C14 product often outperforms its shorter homologues.
In one case, a customer sought to formulate a water-in-oil microemulsion using 1-butyl-3-methylimidazolium bromide. Phase separation proved stubborn. Swapping in 1-tetradecyl-3-methylimidazolium bromide, under identical processing, facilitated rapid clear phase formation and delivered long-term stability under stress testing—a real result, not a brochure claim. Our technical support department actually tracked both batches from raw materials to application testing, confirming that the longer alkyl chain made all the difference.
The first thing anyone notices handling this compound is its waxy, semi-solid state at room temperature. Contrast that with the lower melting, almost oily short-chain derivatives. Packaging staff here learned early on that ordinary scoop-out container dispensing doesn’t work well if the product sits too long in cold storage—the material develops a thick, almost butter-like consistency. Proper warming under nitrogen and minimal agitation gives a free-flowing substance, so we always recommend shipping cold but instructing users about gentle pre-warming to avoid excessive oxidation or water uptake.
Batches left loosely capped soon turn opaque, hinting at slow water absorption or even micro-crystal precipitation. This isn’t marketing talk—it’s experience from storing poly-kg lots in our own QC archive. Desiccators and tight vapor seals aren’t optional; they’re essential tools that save R&D teams from headaches when accurate weighing and reproducible experiments matter. Laboratory partners have thanked us for this advice, which came at the expense of a few ruined early batches before we zeroed in on storage protocols.
While other manufacturers sometimes settle for technical-grade output, our reputation grew from a commitment to research-grade material. Analytical characterization goes beyond a fast TLC or melting point. Every consignment, whether destined for academic research or specialty synthesis, ships with NMR, elemental analysis, and a certificate of water content as standard. Analytical failures, no matter how minor, trigger a root-cause report and a voluntary batch recall from our inventory.
Our chemists have worked with process engineers to streamline the final purification, which for this compound means a combination of activated charcoal polish and vacuum distillation—steps that add cost, but remove traces of colored by-products left from quaternization. Unlike more volatile ionic liquids, tetradecyl-imidazolium bromide’s melting and decomposition points demand tight temperature and vacuum controls, and this knowledge only grows with repeated scale-ups. Years of optimizing these systems taught us that the last few tenths of a percent in purity make or break both application results and regulatory acceptance.
The diversity of end uses for this compound comes up again and again in our customer consultations. One week, it’s a team in battery development investigating its use as an additive for lithium-ion electrolytes. The following week, a wastewater treatment plant requests several kilograms for a pilot on heavy metal extraction. The next order, it’s a cosmetics researcher probing the material’s gentle cationic surfactant properties for a cleansing balm meant to avoid PEG polymers. This product gets pulled in many directions, and our production management must be flexible to meet those windows without quality trade-offs.
Customers in extractions or catalysis often describe how competing ionic liquids fail to solubilize specific organic or inorganic compounds. The tetradecyl chain’s extra length brings not only hydrophobicity; it allows people to tune microphase environments, stabilize reactive intermediates, and gain reproducible kinetics, especially in surfactant-rich conditions. In synthesis of responsive gels, its unique self-assembly becomes a backbone for more advanced smart materials. Feedback from both academic and industrial partners keeps shaping our production decisions, and each anecdote guides improvements for future batches.
Despite many strengths, honest discussion about this compound’s quirks matters. Solubility, for example, doesn’t always follow a simple rule. Some solvents foster rapid dissolution—a feature that makes scale-up easier—while others leave stubborn clumps that must be coaxed apart. Staff technicians routinely evaluate solvent compatibility on each batch, and our technical documentation includes their notes about odd cases or outlier results, not just “off-the-shelf” values.
Another point that comes up is toxicity and environmental safety. Although the imidazolium class often replaces volatile organics in green chemistry circles, long-chain derivatives such as this one require thoughtful handling. Safety data sheets highlight potential aquatic toxicity, and our compliance team stays vigilant about emerging regulations in different jurisdictions. Research is ongoing into full life-cycle analysis, and we routinely support lab-scale studies of degradability, bioaccumulation, and alternative disposal. These challenges push us to collaborate both with customers and academic partners seeking new bio-based cationic surfactants.
Scaling up preparation of 1-Tetradecyl-3-methylimidazolium bromide is not a straightforward task. Compared with smaller imidazolium analogues, this compound’s synthesis intensifies as chain length increases. Pilot-scale reactors must maintain strict temperature control; the exothermic quaternization runs hot, so we install jacketed vessels with real-time heat feedback. Impurities from incomplete reactions or unreacted starting materials prove more stubborn with each scale jump, so purification strategies evolve from simple filtration to staged extractions and careful distillation under controlled vacuum.
Our operations team debates reactor charge rates, as slower addition fosters better mixing and narrows the impurity profile. Every year, we review the latest literature and in-house studies to refine catalyst and solvent choices—always targeting lower process waste, safer handling, and better environmental compatibility. We see ourselves not just as producers selling a commodity, but as partners helping to advance the science of ionic liquids by reporting what works and—just as important—what doesn’t.
It’s easy to lose perspective if you only see your product leave the shipping dock. That’s why we stay in touch after delivery, seeking honest assessments from every recipient. Researchers who compare our 1-Tetradecyl-3-methylimidazolium bromide side-by-side with competitors often mention the predictability of melting points, minimal odorous by-products, and lower residue after solvent evaporation. Graduate students advise us about batch-specific quirks, which QC teams track in our production logs for ongoing process adjustments.
We received valuable feedback about film formation rates in spin-casting experiments, leading our process engineers to rethink drying conditions and storage containers. Our annual reviews of return merchandise and customer complaints, rare but important, have inspired at least two improvements in packaging and batch labeling. These changes come from real-world testing, and they’re logged in our quality management database for future reference.
1-Butyl-3-methylimidazolium bromide serves as the shorter homolog and often acts as an initial screening material in phase transfer and solvent studies. Yet, our customers moving to more exacting application spaces—those demanding lower vapor pressure, larger hydrophobic domains, or formation of more stable colloids—often migrate to the tetradecyl variant. The longer chain improves structuring behavior and broadens the operational temperature window, but it also brings new handling and purification challenges, which compel a higher level of manufacturing vigilance.
Against commonly used quaternary ammonium surfactants, the imidazolium core presents wider chemical compatibility and better thermal stability, key for users working in high-temperature or chemically aggressive conditions. Direct experience in our pilot reactors making both classes of compounds made clear the trade-offs in cost, scale, and downstream purification. Our process teams document the unique filtration and solvent switch requirements for each, so users benefit from non-theoretical, in-the-trenches guidance that saves time in application development.
No two production runs look exactly the same, even with rigid SOPs and validated equipment. Batch chemists review every new feedstock for subtle changes—chain-length distribution, odorous residues from older starting materials, and purity of the methylating agents. Differences in atmospheric humidity on the day of crystallization subtly impact final water content, so our staff measures and logs everything, sharing best practices with users working in similarly humidity-sensitive environments.
We keep a detailed long-term archive of past batches, not just for regulatory reasons but as part of a learning culture. Pattern analysis from these records highlights correlations between ambient temperature swings and occasional batch-to-batch texture variances. Sharing these findings with customers lets us jointly refine storage and use protocols, preventing wasted hours spent troubleshooting unexplained inconsistencies in downstream work.
Much of our customer support revolves around practical issues—solubility hiccups, scale-up advice, or the transition from laboratory bench to pilot runs. We keep lines open for real chemists working through tough formulations, providing technical bulletins based directly on cases from our own process optimization or customer-reported test results. Rather than repeating documentation, we send lab snapshots showing how we resolve foaming, clumping, or unexpected phase behaviors during mixing or solvent exchange. Our technical support isn’t just a call center; it’s staffed by hands-on chemists sharing their solutions and occasionally troubleshooting right next to end users.
For newcomers to ionic liquids, we advocate careful titration and staged mixing, echoing methods our own QC labs use daily. Years of assisting hundreds of formulation projects have shown us that small, incremental adjustments—working up from bench vials to full liter or kilogram-scale lots—help avoid pitfalls. Adjusting water content, pre-conditioning the compound, and tweaking buffer ions often mean the difference between a frustrating day and a breakthrough result. Our teams walk users through these processes, learning together how to stretch the utility of this chemistry into new domains.
Our role in the chain doesn’t end with a single delivery. We foster relationships through joint trials, publishing case studies on recent uses in catalysis and nanomaterial stabilization. Customers with unusual requirements for purity, particle size, or blending tolerance drive lab-scale projects that offer findings fed straight into process adjustments. Each new field test, whether successful or a challenge, gives us more data and, just as important, confidence in how to better serve the next project or market pivot.
We’ve partnered with universities investigating new uses for long-chain imidazolium salts in CO2 capture, heavy metal remediation, and drug delivery research. Real-world constraints—batch stability, operational temperature swings, and regulatory concerns—shape our product refinement. This open feedback loop keeps innovation grounded in achievable and reproducible results, moving product development beyond the drawing board into daily use.
The demand for well-characterized ionic liquids keeps rising, especially as industries move away from hazardous solvents and legacy surfactants. Our operations group remains vigilant about supply chain risks, regulatory shifts, and scale-up side effects, always tailoring improvements to actual user needs rather than market fads. Investments in emission controls, on-site renewable energy, and closed-loop solvent systems stem directly from the urge to make responsible chemistry, not just marketable product.
Industry standards keep evolving, and in the spirit of continuous learning, we seek ways to document the environmental impact and safety profile of each batch—not only to satisfy regulatory authorities but because shared transparency keeps us accountable to every customer, large or small.
Making 1-Tetradecyl-3-methylimidazolium bromide amounts to more than pouring chemicals and bottling the result. Years of trial, adaptation, and customer interaction shaped our understanding about what truly matters: reproducibility, practical support, and the willingness to admit where improvement is needed. Long-chain imidazolium compounds like this one offer unique strengths, but their value depends entirely on rigorous, experienced manufacturing, vigilant quality control, and a culture open to feedback and change. We produce this product not as a faceless volume supplier, but as a partner navigating chemistry—and its endless practical challenges—side by side with the people who put our work to the test in the real world.