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HS Code |
788549 |
| Chemical Name | 1-Hexyl-3-Vinylimidazolium Bromide |
| Cas Number | 778711-72-1 |
| Molecular Formula | C11H19BrN2 |
| Molecular Weight | 259.19 g/mol |
| Appearance | White to off-white crystalline powder |
| Melting Point | Approx. 90-100°C |
| Solubility In Water | Soluble |
| Purity | Typically >98% |
| Storage Temperature | Room temperature, dry conditions |
| Synonyms | HVIM Br; 1-Hexyl-3-Vinylimidazolium Bromide |
| Smiles | C1=CN(C(=N1)CCCCCC)C=C.Br |
| Density | Approximately 1.2 g/cm³ |
| Inchi | InChI=1S/C11H19N2.BrH/c1-3-4-5-6-8-13-10-12-9-11(13)7-2;/h7,9-10H,2-6,8H2,1H3;1H |
As an accredited 1-Hexyl-3-Vinylimidazolium Bromide factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | A 25g amber glass bottle tightly sealed, labeled “1-Hexyl-3-Vinylimidazolium Bromide,” with hazard warnings and lot number displayed. |
| Shipping | 1-Hexyl-3-vinylimidazolium bromide is shipped in tightly sealed containers, stored in a cool, dry place away from direct sunlight and moisture. The chemical is handled according to standard hazardous material protocols, ensuring proper labeling and documentation for transport. Use appropriate personal protective equipment when handling the package. |
| Storage | 1-Hexyl-3-vinylimidazolium bromide should be stored in a tightly sealed container in a cool, dry, and well-ventilated area, away from sources of ignition and moisture. Protect from direct sunlight and incompatible substances such as strong oxidizers. Store at room temperature and avoid excessive heat. Use appropriate chemical storage cabinets for added safety and clearly label the container. |
Applications of 1-Hexyl-3-Vinylimidazolium Bromide in Industrial ManufacturingAs a direct manufacturer of 1-Hexyl-3-Vinylimidazolium Bromide, we supply global producers with this ionic liquid for demanding process environments. Its unique structural and chemical properties support advanced synthesis, electrochemical, and separation processes. We highlight below the main downstream applications, indicating standardized industry requirements, main formulation ranges, integration steps, and typical end products. 1. Electrolyte Additive for Supercapacitors and Energy Storage DevicesManufacturers incorporate this ionic liquid as an electrolyte additive to enhance cycle stability, ionic conductivity, and operational voltage range in double-layer capacitors and hybrid storage devices. During the mixing stage, formulators balance the ratio based on cell design, electrode material, and target operating temperature. This approach ensures stable device performance under varied load cycles and reduces hazards compared to traditional volatile electrolytes. Industry compliance standards
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2. Solvent and Phase-Transfer Catalyst in Organic SynthesisChemical manufacturers leverage ionic liquids of this structure as reaction media and phase-transfer agents to facilitate alkylation, halogenation, and cross-coupling reactions, especially those involving immiscible solvents. This material withstands elevated temperatures, minimizes byproduct formation, and enables easier product isolation with improved yields, especially in the synthesis of complex intermediates for pharmaceuticals, agrochemicals, and advanced polymers. Industry compliance standards
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3. Ionic Liquid for Extraction and Separation in Rare Earth and Metal ProcessingMetal refineries utilize this compound as a selective extraction medium in liquid-liquid separation and solvent extraction processes. Its high selectivity for lanthanides, actinides, and certain transition metals allows efficient separation from complex ore matrices and leachates. By replacing traditional organic solvents, it reduces both VOC emissions and secondary waste challenges, thus optimizing operational safety and environmental performance in critical metal purification. Industry compliance standards
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4. Polymerization Medium and Template Agent in Advanced Polymer SynthesisProducers of advanced polymers employ this ionic liquid as a functionalized medium and structural template in the synthesis of polyelectrolytes, ionic polymers, and functional block copolymers. Its vinyl group enables co-polymerization, creating materials with tunable conductivity, enhanced solubility, and improved anti-static characteristics. Process engineers control viscosity, chain length, and reaction rate in both batch and continuous processes to achieve final material specifications. Industry compliance standards
Typical usage ratio
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Years spent scaling up ionic liquid production have shown us that only durable products survive in research and industry. We see 1-Hexyl-3-vinylimidazolium Bromide, often recognized by researchers for its combination of hydrophobic and vinyl-functional properties, carving out a firm position within the broader family of imidazolium-based ionic liquids. In actual plant conditions, reliability means more than a list of specifications. Every batch comes down to handling, purity, and how well a compound achieves results for chemists and engineers doing real work on site.
We produce 1-Hexyl-3-vinylimidazolium Bromide as a clear, slightly viscous liquid, with a pale yellow tint showing up only when storage extends past optimum conditions. Molecular weight sits at roughly 323.30 g/mol, and the structure links a six-carbon hexyl chain and a vinyl group to the imidazolium core, with bromide as the counterion. We select each reagent grade right down to trace metals content, aiming to minimize byproducts or water content—key for groups developing sensitive catalysts or ionic polymer electrolytes.
Water content remains a consistent focus. Even trace moisture can start to shift reactivity in electrochemical and polymerization experiments. We maintain every batch below 0.2% water by Karl Fischer titration. Residual solvents, if any, fall below detection in NMR and GC-MS. Our quality control matches lot-to-lot spectral signatures for 1H NMR, confirming both the hexyl and vinyl groups. It’s not uncommon for researchers to ask for COA-grade purity results with each order, and we find that these details matter most when projects scale beyond bench synthesis.
The versatility of 1-Hexyl-3-vinylimidazolium Bromide starts with its dual reactivity. That vinyl group earns its keep in polymer chemistry, where it serves as a functional monomer or ionic crosslinker. Polymer scientists spin this compound into ion-conductive membranes, water treatment materials, and responsive hydrogels, dialing up performance by leveraging the imidazolium moiety’s ionic character. We’ve shipped this product to teams researching advanced lithium batteries, where improved ionic transport can directly affect cycle life and cathode stability.
Pharmaceutical and fine chemical development also draw on this compound. The long alkyl chain modulates solubility, making separation tasks or catalyst recycling more practical compared to shorter analogues. In phase-transfer catalysis, we’ve seen customers report increased turnover numbers, sometimes paired with longer catalyst lifetimes. The bromide, despite being a common anion, can outperform PF6 or BF4 in reactions where halide participation aids selectivity.
Academic groups often choose our 1-Hexyl-3-vinylimidazolium Bromide for ionic liquid-based sensors, membrane fabrication, and as a reaction medium for challenging transition metal catalysis. Its thermal stability and non-volatility allow researchers to avoid solvent losses during reactions above 100°C. Lately, environmental chemistry projects focus on the reusability and phase behavior of ionic liquids; our customers provide feedback on recyclability and leaching, letting us adjust synthesis procedures for even lower impurity carryover.
A wide field of imidazolium ionic liquids now spans simple [BMIM] to more exotic bis(triflimide) analogues. Adding the vinyl functionality opens different doors. Polymeric applications demand functional handles, and the standard alkylimidazoliums can’t covalently bond into a growing network. The vinyl group enables copolymerization with acrylates, styrenics, or even direct UV-induced crosslinking. Single-ion conductors formed this way often achieve higher cationic transport numbers, and the resulting polymers do not leach the ionic liquid during repeated cycles.
We’ve tested batches side-by-side with [BMIM]Br and [HMIM]Br in dye-sensitized solar cell fabrication and observed that our vinylimidazolium outperforms these in ionic conductivity and mechanical stability when incorporated into gel electrolytes. In water treatment research, the longer alkyl chain improves hydrophobicity and surface compatibility with polymer supports. For scientists frustrated by phase separation and limited compatibility with solvents, this product brings improved miscibility with both organic and aqueous phases without compromising thermal stability.
Logistics and storage often get overlooked when new products debut. 1-Hexyl-3-vinylimidazolium Bromide, like most ionic liquids, absorbs moisture readily. We ship in airtight containers with argon or dry nitrogen backfill, especially for export. It stores well for over a year at room temperature if kept sealed, but exposure to open air will draw moisture, which drops purity over time. Our warehouse moves product directly from synthesis vessel to airtight drum, minimizing time spent in transfer tanks.
Some customers want this compound in larger scale, upwards of 20 kg. Handling bulk liquid ionic salts presents its own hurdles, especially viscosity management and pumping. We have long switched to high-shear mixers and jacketed reactors to avoid cold-weather congealing or inhomogeneous mixing. The vinyl group brings an extra layer of care: sunlight and radical contamination can start slow, unwanted polymerization during long-term storage. All bulk shipments ship in opaque drums, and our operators always check peroxides and oxygen levels whenever drums are recirculated.
Research, especially in ionic liquid and polymer science, thrives on reproducibility. Our own technical team keeps a feedback loop open with academic and industrial groups. When unexpected color changes or viscosity shifts crop up, we partner with users to trace impurities or degradation routes. A research group working on membrane modification reported oxidative discoloration over months. Our post-shipment analytical team traced the issue to excess headspace oxygen in storage drums—a tweak in our purge protocols resolved it for all new orders.
Sharing our QC data with every shipment has resulted in a deeper trust base. Customers set up validation on their end, cross-referencing our COA readings with in-house NMR or ion chromatography. If batches show deviation, we adjust purification steps and flag lots for rework rather than risk downstream project failures. Long-term partners say this transparency saved weeks if not months of troubleshooting in scale-up.
Bromide-based ionic liquids bring their own environmental exposure points. We focus on minimal aqueous waste during workup and encourage customers to follow best laboratory practices for disposal and recycling. Our own process development aims to reduce halogenated byproduct streams, and filtration steps keep trace halides well below regulatory thresholds. Aromatic imidazolium-based liquids resist simple microbial breakdown, raising concerns that end-users are now addressing with advanced oxidants and multi-stage biotreatment. We track all local and international regulations and have never had a shipment stopped for non-compliance.
Years of in-plant handling taught us to focus on skin contact risks and eye sensitivity. Safety protocols rely on chemical goggles and NBR gloves, with eye wash stations set at every filling line. Our team never downplays the potential for mild irritation or allergic reaction—each new operator receives specific training for ionic liquids, beyond standard chemical hygiene. Rare spills clean up easily with absorbents and thorough soap washing, though prompt attention makes all the difference.
Market demand for 1-Hexyl-3-vinylimidazolium Bromide doesn’t match commodity chemicals, but its unique functionality supports a premium. Our scaling approach leverages continuous-flow reactors and high-purity filtration, striking a compromise between batch-to-batch reproducibility and flexible order sizes. These tools also let us respond quickly if a project suddenly grows; batch lead times stay under five weeks, even during peak procurement cycles.
Feedstock volatility, especially for base imidazole and brominating reagents, sometimes impacts raw material costs. We’ve negotiated with upstream suppliers for locked quotas, so most regular customers don’t see abrupt price hikes. We monitor global trends for lithium-ion batteries and advanced polymers, since spikes in those sectors often translate to higher demand and tighter markets for intermediates like this one.
Research and development teams inside and outside our company keep pushing the limits of what 1-Hexyl-3-vinylimidazolium Bromide can do. Interest is growing fast in green chemistry—swapping out volatile organic solvents for ionic liquids in reaction media to cut workplace hazards and emissions. Many sectors treat ionic liquids as the future of sustainable process design, yet each application hinges on access to a clean, well-characterized supply.
Environmental researchers have started to explore recycling and regeneration strategies. The vinyl functionality allows for recovery and subsequent repolymerization, a big step forward from older ionic liquids that permanently leach into effluent. Pilot projects highlight improved separation after capture cycles and suggest multi-year operational windows if handled correctly.
Improvements on the production floor often spring from cooperation with customers. We get routine requests: increased scale, tailored water content, or customizing the counterion for specific compatibility. Every year, new collaborative projects pop up between our team and research partners—developing mixed-matrix membranes, high-stability supercapacitors, or catalytic coatings with extended working lives. What keeps these efforts moving forward is a strong, two-way feedback system. We not only track what goes out of our facility but follow up with downstream results, listening and adapting to real-world technical challenges.
Our confidence in 1-Hexyl-3-vinylimidazolium Bromide doesn’t arise from theory alone. We’ve invested years refining synthesis routes, improving yields, and tuning purification steps to answer chemists’ practical needs. Every improvement—whether it comes from a customer suggestion or from post-mortem batch analysis—feeds back into our production protocols. There’s no substitute for learning from mistakes and applying those lessons immediately.
Feedback forms the core of our operational model. Routine surveys to frequent buyers ask about unexpected side reactions, storage difficulties, or changes in transport timelines. If a report points to an issue with solubility during polymer preparation, our technical team digs into it and tweaks the next lot’s washing conditions or solvent removal rates. This level of detail comes from a manufacturing team that keeps one foot in the production plant and another in the lab—a perspective traders or resellers rarely maintain.
For chemists exploring energy materials, polymers, or unique electrolyte systems, 1-Hexyl-3-vinylimidazolium Bromide offers scope for exploration paired with a proven track record. We expect future demand to expand as more industries recognize the long-term savings and practical benefits of high-quality ionic liquids. The foundation for this growth remains the shared experience of producers and users, working together through technical hurdles and occasional surprises. Our doors stay open to collaboration and honest discussions, because that’s how lasting progress in specialty chemicals always happens.