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1-Allyl-3-Vinylimidazolium Chloride

    • Product Name 1-Allyl-3-Vinylimidazolium Chloride
    • Alias [AVIM]Cl
    • Einecs 946-304-5
    • 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
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    Specifications

    HS Code

    889869

    Chemical Name 1-Allyl-3-Vinylimidazolium Chloride
    Cas Number 872365-29-6
    Molecular Formula C8H11ClN2
    Molecular Weight 170.64 g/mol
    Appearance White to off-white solid
    Melting Point Approx. 80-120 °C (may vary by purity/source)
    Solubility Soluble in water
    Boiling Point Decomposes before boiling
    Purity Typically >97% (varies by supplier)
    Structural Formula C=C[N+]1=CN(C=C1)C=CC.Cl-
    Storage Store at room temperature in a tightly closed container
    Synonyms 1-allyl-3-vinyl-1H-imidazol-3-ium chloride

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

    Packing & Storage
    Packing 500g of 1-Allyl-3-Vinylimidazolium Chloride is packaged in a sealed, amber glass bottle with a secure screw-cap lid.
    Shipping 1-Allyl-3-Vinylimidazolium Chloride is shipped in tightly sealed, chemically resistant containers to prevent moisture and contamination. The packaging complies with relevant safety regulations for handling ionic liquids. The shipment includes appropriate labeling, safety data sheets, and is usually transported under ambient conditions unless specific hazards require additional precautions.
    Storage 1-Allyl-3-vinylimidazolium chloride should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from moisture and incompatible substances like strong oxidizing agents. Protect the chemical from direct sunlight and sources of ignition. Ensure containers are clearly labeled and kept away from heat to prevent decomposition or hazardous reactions. Store at room temperature unless otherwise specified.
    Application of 1-Allyl-3-Vinylimidazolium Chloride

    Applications of 1-Allyl-3-Vinylimidazolium Chloride in Industrial Manufacturing

    1-Allyl-3-Vinylimidazolium Chloride serves as a functional ionic liquid in multiple advanced manufacturing processes. As the original producer, we supply this material directly to global industries requiring high-purity raw inputs for specialized downstream applications. The sections below outline practical industrial use cases across various sectors with detailed compliance, formulation, process, and product information for each.

    1. Polymer Electrolyte Research and Production

    This material plays a key role as a functional ionic liquid monomer in the production of polymer electrolytes for advanced batteries and supercapacitors. During copolymerization, it provides ionic conductivity, thermal stability, and processable mechanical properties. Manufacturers in the energy storage sector utilize it to engineer high-performance gel and solid-state electrolytes, responding to growing demand from lithium-ion and next-generation battery applications.

    Industry compliance standards

    • IEC 62660-2 (Secondary lithium-ion cells for industrial batteries)
    • UN 38.3 (Transport of Dangerous Goods – Lithium Cells)
    • ISO 9001:2015 (Quality Management in Electrode Manufacturing)
    • ROHS Directive (Restriction of Hazardous Substances, for electronics integration)

    Typical usage ratio

    • 5–20 wt% as an ionic monomer in copolymer matrices, adjusted based on target ionic conductivity and viscosity. Quantities depend on polymer backbone compatibility and application (gel vs solid electrolytes).

    Downstream process integration

    • Added during in-situ or ex-situ polymerization with acrylate, methacrylate, or vinyl backbones. Functions as a co-monomer and conducting component prior to cross-linking and solvent removal steps.

    Final product types

    • Solid-state lithium battery packs
    • Supercapacitor modules
    • Flexible wearable electronics power cells
    • Stationary energy storage systems

    2. Ion Exchange Membrane Fabrication

    This ionic liquid functions as a performance modifier and conductivity aid in ion exchange membranes manufactured for fuel cells and chemical process separation. Proprietary formulations with this raw material allow membrane producers to tailor selectivity, ionic conductivity, and mechanical stability for demanding gas or liquid phase operations. Its use underpins efficiency improvements and durability enhancements in hydrogen energy infrastructure and industrial filtration units.

    Industry compliance standards

    • IEC 62282-2 (Fuel Cell Technologies – PEM Module Testing)
    • ISO 14001:2015 (Environmental Management for chemical processing)
    • REACH Regulation (EC) No 1907/2006
    • ASTM D3860 (Membranes for Industrial Separations)

    Typical usage ratio

    • 1–10 mol% as a dopant or functional group, depending on membrane thickness, polymer type, and end-use water content stability requirements.

    Downstream process integration

    • Blended into membrane casting solutions or directly copolymerized with base monomers. Incorporated before solvent evaporation and crosslinking under controlled humidity and temperature conditions.

    Final product types

    • Proton-exchange membranes for fuel cells
    • Anion-exchange membranes for electrolyzers
    • Industrial dialyzers and separation modules
    • High-capacity desalination or water treatment units

    3. Antistatic Coating Formulations for Electronics

    Manufacturers of coatings and films for electronic devices integrate this ionic liquid as an antistatic additive to impart durable conductivity in polymeric surfaces. The material’s imidazolium structure enables strong ionic mobility, ensuring long-term surface discharge capabilities. Its controlled use allows film and coating producers to meet exact customer ESD (electrostatic discharge) resistance targets in cleanroom, electronics assembly, and packaging applications.

    Industry compliance standards

    • IEC 61340-5-1 (ESD Control in Electronics Manufacturing)
    • JIS L1094 (Antistatic Performance Standards)
    • ISO 22196 (Antimicrobial Efficacy – Plastic Surfaces, where relevant)
    • RoHS Directive (Restriction of Hazardous Substances)

    Typical usage ratio

    • 0.5–3 wt% in waterborne or solventborne polymer coating matrices. Adjusted to achieve surface resistivity in the range of 106–1010 ohms per square, depending on the final substrate and application environment.

    Downstream process integration

    • Added during formulation blending with acrylic, polyurethane, or epoxy resins. Typically introduced before pigment dispersion to avoid agglomeration and retain uniform ionic distribution in the cured film layer.

    Final product types

    • Antistatic floor coatings for electronics factories
    • Protective films for TFT-LCD manufacturing
    • Device enclosure coatings
    • ESD-safe workbench mats and cleanroom goods

    4. Catalysis and Phase Transfer Systems in Organic Synthesis

    Chemical synthesis plants employ this material as a phase transfer catalyst and ionic reaction medium in advanced organic transformations. Its high polarity and wide electrochemical window enable efficient alkylation, polymerization, and metathesis reactions. Unlike standard quaternary ammonium salts, the imidazolium chloride structure enhances anion transport and organic phase compatibility, improving yields in pharmaceutical intermediate or specialty chemical production.

    Industry compliance standards

    • Current Good Manufacturing Practice (cGMP, for pharma applications)
    • 21 CFR Part 211 (Pharmaceutical Production Control, US FDA)
    • ISO 22541 (Fine Chemicals Quality Control)
    • REACH Regulation (EU registration for chemical substances)

    Typical usage ratio

    • 0.1–5 mol% relative to limiting reagent. The specific addition depends on substrate reactivity, solvent system, and targeted turnover frequency for the catalytic step.

    Downstream process integration

    • Dosed to reaction vessels at the mixing or activation stage. In continuous processes, metered to maintain steady catalytic activity or phase transfer properties during process flow.

    Final product types

    • Pharmaceutical intermediates (e.g., active ingredient precursors)
    • Agrochemical building blocks
    • High-purity specialty chemicals
    • Advanced polymer precursors

    5. Additive for Functionalized Polymer Synthesis

    Industrial polymerization units use this compound to synthesize specialty polymers with tailored ionic or hydrophilic domains. Its integration as a co-monomer or chain modifier provides water solubility, ion-exchange behavior, and chemical tunability. Resin plants manufacturing polyelectrolyte complexes, hydrogels, or functionalized membranes depend on batch-wise or continuous dosing to develop unique material properties meeting diverse market needs.

    Industry compliance standards

    • ISO 9001:2015 (Quality Management in Polymer Manufacturing)
    • EN 14041 (Resilient Floor Coverings Compliance, if flooring is targeted)
    • REACH Regulation (European Union Chemical Safety)
    • ASTM D883 (Standard Terminology for Plastics)

    Typical usage ratio

    • 2–15 mol% of total monomer mix, modulated according to target ion content, mechanical properties, and final product solubility/hydrophobicity demands.

    Downstream process integration

    • Introduced directly to the polymerization kettle or bulk reactor with vinyl, acrylate, or other functional monomers. Blending and feeding rates optimized for uniform copolymer structure, monitored by in-line IR or NMR analysis.

    Final product types

    • Superabsorbent polymers
    • Ion-exchange resin beads
    • Hydrogel wound dressings (non-medical)
    • Functionalized filtration membranes
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    Certification & Compliance
    More Introduction

    1-Allyl-3-Vinylimidazolium Chloride: Pushing Boundaries in Specialty Chemistry

    A Fresh Take on Ionic Liquids

    Chemists often search for workhorses that do more than just fill a role. 1-Allyl-3-Vinylimidazolium Chloride stands out in that crowd. We’ve seen our customers in polymer research and advanced materials ask for ionic liquids that offer both flexibility and reactivity. Through years of synthesis and scale-up work, our team has fine-tuned this compound—delivering a product that keeps its performance consistent from the lab bench to pilot plants. The appeal hinges on a truly unique cation, blending both allyl and vinyl functionalities. These are more than labels for us: in practical terms, this chemical lets end-users explore polymerization strategies and chemical modification paths that standard imidazolium salts simply can’t reach.

    The Model We Trust: Purity and Practicality

    We produce 1-Allyl-3-Vinylimidazolium Chloride to offer not just one grade. Researchers chasing late-stage functionalization demand tight purity specifications. We know water content and trace metallic impurities easily disrupt polymerization. Each batch gets tested with NMR and HPLC, results recorded, and we let customers review the summary certificate. Our default model stabilizes at a high-purity solid, sealed under inert gas at shipment. For clients working in aqueous media, we’re able to hydrate the salt to specific moisture levels without introducing chloride or other counter-ions that complicate downstream processing. Our formulation routes avoid organic halide residues and do not rely on commercial-grade precursors. All synthesis steps take place in reactors that undergo verification between campaigns—no carryover, no leaching.

    What Sets 1-Allyl-3-Vinylimidazolium Chloride Apart?

    Experience in ionic liquid chemistry brings lessons you can’t learn from a database. Imidazolium salts themselves have become almost a commodity—some lack the versatility needed as building blocks. By combining allyl and vinyl groups on the imidazolium ring, our compound changes the game. Both moieties participate directly in radical, cationic, or anionic polymerizations, giving researchers a two-pronged functionality that rarely comes in a single molecule. Compared to more basic imidazolium salts, such as 1-ethyl-3-methylimidazolium chloride or butyl analogs, this version can graft itself onto polymer backbones or serve as a reactive site for further chemical elaboration. Vinyl functionality opens the door to radical chain growth, and allyl gives access to thiol-ene and similar click reactions. We notice many exploratory studies on polyelectrolyte networks, hydrogels, and membranes gravitate toward this material because of that dual potential.

    Because our process runs solvent-free for much of the synthesis, we maintain control over the degree of substitution—avoiding mixed isomers or unintended crosslinking. Traditional imidazolium salts offer little more than charge stabilization or a polar medium. Our product can integrate into polymer matrices, either as a comonomer or a charged pendant group, something standard ionic liquids struggle to do without modification. Customers working with specialty coatings and electroactive films depend on this difference. Some labs report successful use in ion-conducting membranes, where both the charge and functionality support performance beyond what conventional imidazolium salts deliver.

    Real-World Applications and End-User Insights

    In our own pilot facility, this salt has played a starring role in functional polymer development. We’ve supported academic labs and private R&D teams experimenting with polyelectrolyte blocks, where the vinyl and allyl sites co-polymerize with styrene or acrylate monomers. One benefit we noticed: the absence of aromatic by-products, which can interfere in high-precision spectroscopy or downstream purification.

    Industrial researchers focused on ion-exchange membranes found 1-Allyl-3-Vinylimidazolium Chloride to be more effective than basic imidazolium salts for tailoring ionic conductivity. The vinyl group enables strong backbone bonding, reducing the risk of leaching or migration. Because this product can be immobilized inside a polymer network, end-use devices, like sensors and environmental remediation cartridges, show prolonged performance without experiencing the bleed-out found with standard ionic liquids.

    There has also been substantial uptake in click-chemistry workflows. Having the allyl group integrated in the cationic component means there’s no need for two separate functional materials. Technicians report smoother reaction monitoring and higher throughput, especially in thiol-ene or Michael addition schemes. Studies in the literature cite faster reaction rates due to lower steric hindrance on the ring substituents—a detail we’ve also confirmed through our own QA trials.

    Supporting Innovation in Materials Science

    Many of our large-batch users are universities and corporate labs working on energy storage, water treatment, and functional coatings. By providing a chloride salt, the most common counter-ion, we make sure solubility in water and polar organics remains straightforward. Our formulation doesn’t rely on excess stabilizers or phthalate residues, which can plague competing products. Modified cellulose, chitosan, or PEGylated scaffolds have all proven compatible. These findings come directly from feedback and collaborative development work with customers aiming for novel architectures.

    There’s a growing interest in sustainable chemistry. We consider lifecycle impact right from the early synthetic stages. Using anhydrous conditions and closed-loop purification, we avoid generating unnecessary halide waste. Process analysts within our team have identified several areas where energy use drops by running at ambient pressure, rather than relying on vacuum stages common with older protocols.

    Polymer science keeps evolving. Our chemistry team has fielded requests for homologated analogs with altered alkene substitution—proof that researchers are expanding well beyond the old toolbox. That said, the vinyl-allyl option brings a sweet spot of reactivity and processability that suits many emerging challenges in membranes and gel electrolytes.

    Challenges and Solutions from the Manufacturing Floor

    Scaling a specialty ionic liquid brings hurdles that can’t always be solved by standard protocols. Early in our process development, residual halides and unreacted precursors posed risks for applications requiring strict electrochemical purity. By adding batchwise monitoring and in-line titration, we pinpointed stages where contaminants might slip through. Data from these monitoring efforts have fed directly into our lot-release criteria—rather than waiting until the end, we tackle problems mid-process.

    Logistics also require attention. Ionic liquids can attract moisture during packaging, altering their flow properties and reactivity profiles. We adopted high-barrier laminate packaging with inert gas purging so every shipment remains within specification, even after weeks in transit. On arrival, customers comment on the material’s free-flowing nature and consistent appearance, factors that reflect the controls we keep in place from synthesis onward.

    Reproducibility ranks as a top concern among our R&D partners. Unlike commodity chemical companies, we make every batch record available for customer review and welcome feedback via direct technical support. Our production management team maintains a rolling library of retention samples. If discrepancies ever come up, we compare fresh samples against our own stores to resolve any issues and keep trust solid on both sides.

    Comparing to Other Functional Imidazolium Salts

    Standard imidazolium chlorides, like methyl- or butyl-substituted versions, occupy many catalogues and handle basic solvent and electrochemical tasks well. In practice, these compounds have limited usefulness for direct chemical grafting. Their lack of unsaturation stymies creative work in polymer workflows. Imidazolium salts with an additional functional handle often require post-synthesis modification—more steps, more cost, more error potential. Our 1-Allyl-3-Vinylimidazolium Chloride stands apart because both reactive sites arrive pre-installed. That means fewer pre-polymerization steps and higher yields in the downstream process.

    Some labs have tried to mimic the dual-functional structure using mixtures of different ionic liquids, but the results never match what you get from a single, clean, cationic entity. Incompatibility and phase separation limit those approaches. That feedback comes directly from formulators who’ve attempted side-by-side comparisons in both crosslinking and membrane casting experiments.

    Why Direct Manufacturing Matters

    Third-party resellers sometimes introduce unexpected variables—unverified storage practices, unknown provenance, inconsistent quality from lot to lot. By producing 1-Allyl-3-Vinylimidazolium Chloride directly, we keep line-of-sight from raw material sourcing through final shipment. There’s less risk of contamination or mislabeling. Customers benefit from direct technical dialogue, quick access to COAs, and transparency about our process. Relying on a manufacturer rather than a middleman can seem like a small issue, but differences in shelf life, packaging standards, and traceability often add up to significant advantages for front-line researchers.

    Our roots in custom synthesis go back decades. The same teams that build new variants for cutting-edge research continue to oversee batch production and support large-scale partners as project demands grow. When formulation questions arise—solubility in mixed solvents, compatibility with challenging monomers, or behavior under scale-up—our chemists offer practical advice based on hands-on work, not outsourced documentation or guesswork.

    Safety, Environmental Responsibility, and Future Focus

    Handling specialty ionic liquids always calls for respect. 1-Allyl-3-Vinylimidazolium Chloride demands the typical PPE—a lab coat, gloves, eye protection—and benefits from local exhaust if used in bulk. But our synthesis excludes most of the nastier by-products that can complicate disposal. Chloride salts are among the easiest to manage under well-known waste streams, keeping safety protocols clear and manageable even in international shipments.

    Process improvements stay high on our agenda. We track environmental incidents carefully, both within our facilities and among downstream users. Customers have shared with us that regulatory reviews, particularly in the EU and US, have begun to pay closer attention to persistent ionic contaminants. That’s why our in-house analytical team keeps purity above the competition—both to meet legal requirements and to minimize unexpected setbacks during product qualification.

    Our team pursues green chemistry benchmarks, opting for minimal-waste streams, solvent recycling, and real-time monitoring of effluents. We see a direct line between operational discipline and long-term market access. This compound, with its reactivity and straightforward disposal, sits comfortably alongside sustainable process goals. The feedback loops between our synthetic, QA, and supply-chain teams underpin every improvement, and the learning never really stops.

    Supporting Progress Beyond the Laboratory

    Customers who start their work with this compound often bring us new challenges and stretch goals. One university electrochemistry group worked with us to refine membrane doping methods, resulting in consistent performance upticks across hundreds of test cycles. Catalysis labs have documented faster reaction setups when using our salt as an ionic stabilizer, reducing activation times in both organic and aqueous systems. We hear about success with new hydrogel systems, mostly because the dual functionality survives both conventional free-radical and step-growth polymerization protocols.

    We believe in the value of conversation with our users. No two applications seem to use 1-Allyl-3-Vinylimidazolium Chloride exactly the same way, and every project teaches us something new. That cycle—feedback, process refinement, sharing technical findings—has propelled us to keep improving batch after batch. Transparency in testing, reliability in supply, and deep product understanding all matter. That’s how we’ve seen this compound become a mainstay in more than just one segment of the chemistry marketplace.

    The Road Ahead

    As specialty chemicals become more sophisticated and end-users demand broader functionality, molecules like 1-Allyl-3-Vinylimidazolium Chloride will keep pushing the bounds of research and manufacturing. Our team sees direct manufacture not just as an advantage, but as a responsibility—giving every batch the care and oversight needed for advanced materials programs across the globe. The chemistry keeps evolving, and with every step forward, our commitment to quality, innovation, and open exchange with researchers stays front and center.