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1-Propylsulfonic-3-Vinylimidazolium Chloride

    • Product Name 1-Propylsulfonic-3-Vinylimidazolium Chloride
    • Alias PSVIM-Cl
    • Einecs 611-273-3
    • 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

    224889

    Productname 1-Propylsulfonic-3-Vinylimidazolium Chloride
    Casnumber 1040860-45-8
    Molecularformula C8H15ClN2O3S
    Molecularweight 254.74 g/mol
    Appearance White to off-white solid
    Purity Typically ≥98%
    Meltingpoint Decomposes above 200°C
    Solubility Soluble in water
    Storagetemperature Room temperature
    Iupacname 1-(3-sulfopropyl)-3-vinylimidazolium chloride

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

    Packing & Storage
    Packing Sealed amber glass bottle containing 100 grams of 1-Propylsulfonic-3-Vinylimidazolium Chloride, labeled with chemical name, purity, and safety warnings.
    Shipping **Shipping Description:** 1-Propylsulfonic-3-Vinylimidazolium Chloride is shipped in tightly sealed containers to prevent moisture absorption and contamination. It should be stored and transported at room temperature, away from strong oxidizers. Handle with appropriate personal protective equipment. Ensure compliance with local, national, and international chemical transport regulations. Not classified as hazardous for most shipping methods.
    Storage 1-Propylsulfonic-3-vinylimidazolium chloride should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area. Protect from moisture, direct sunlight, and incompatible materials such as strong oxidizing agents. Keep away from heat sources and ignition. Always label the container and use secondary containment to prevent spills. Follow all relevant safety and regulatory storage guidelines.
    Application of 1-Propylsulfonic-3-Vinylimidazolium Chloride

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

    As the direct manufacturer of 1-Propylsulfonic-3-Vinylimidazolium Chloride, we supply this ionic liquid for advanced industrial applications where precise functionalization and catalytic enhancement are critical. Below we outline specialized downstream uses, including detailed compliance, process, and formulation parameters supported by end-product manufacturing references.

    1. Catalytic Material for Acid Functionalized Polymer Electrolyte Membranes

    This raw material is increasingly used by proton exchange membrane (PEM) manufacturers to introduce sulfonic acid groups onto polymer backbones, enhancing ion conductivity for industrial fuel cell systems. It reacts via in-situ polymerization or grafting onto vinyl substrates during membrane casting processes, meeting strict purity and ionic transport control requirements for operational durability.

    Industry compliance standards

    • ASTM D7981 (Standard Test Method for Measuring the Ionic Conductivity of Polymer Electrolyte Membranes)
    • ISO 14687:2019 (Hydrogen fuel — Product specification)
    • IEC 62282-2 (Fuel cell technologies – Part 2: Fuel cell modules)
    • QC/FC 16-2013 (China Fuel Cell Vehicle Industrial Standards)

    Typical usage ratio

    • 2–10 wt% as a monomer/copolymer feed or functional additive, depending on proton conductivity target and substrate type; lower levels for maintenance of mechanical strength.

    Downstream process integration

    • Pre-mixed with vinyl monomers during membrane casting or introduced during copolymerization for functional group attachment, followed by controlled curing and membrane stretching.

    Final product types

    • Proton exchange membrane sheets for stationary fuel cells
    • PEM assemblies for automotive hydrogen fuel cell stacks
    • Electrolyzer separator membranes

    2. Solid Acid Catalyst Precursor in Fine Chemical Synthesis

    Chemical processors utilize this ionic liquid as a sulfonic acid precursor for supported catalyst fabrication where direct covalent attachment is required. It is deployed during grafting or immobilization steps, especially for silica, alumina, or polymer-supported acid catalysts, enabling highly selective alkylation, esterification, or dehydration reactions under anhydrous and mild temperature conditions.

    Industry compliance standards

    • REACH Regulation (EC) No 1907/2006 (EU chemicals safety)
    • ISO 9001:2015 (Chemical production quality management, catalyst division)
    • API Standard 941 (Pressure vessel operation for chemical plant reactions)
    • ICH Q7 (GMP for active pharmaceutical ingredients, for API-grade catalyst use)

    Typical usage ratio

    • Typically 5–15 mol% relative to total support surface sites; lower ratios for high-activity catalysts, up to 20 wt% for strong acidity requirement in batch processes.

    Downstream process integration

    • Impregnated onto solid supports via wet blending or co-polymerization, followed by thermal treatment to anchor sulfonic acid groups before charging catalyst beds.

    Final product types

    • Solid acid catalysts for continuous and batch reactors
    • Acidic ion-exchange resins for pharmaceutical fine chemical production
    • Polymer-supported esterification catalysts for bio-based plastics

    3. Ionic Liquid Component for Green Solvent Systems in Extraction Processes

    Advanced separation facilities select this ionic liquid as a hydrophilic, acid-functional solvent for selective recovery of metals or organics from aqueous solutions, providing both high extraction efficiency and low volatility for closed-loop processes. Its cationic and sulfonic acid moieties confer strong electrostatic interaction and phase separation performance, allowing use under clean solvent initiatives.

    Industry compliance standards

    • OECD Test Guidelines for Chemicals (Solvent selection and environmental safety)
    • EN ISO 14001 (Environmental management systems in chemical processing)
    • US EPA TSCA Inventory (Green chemical use authorization)
    • National Pollution Discharge Elimination System (NPDES, applicable to wastewater discharge from extraction plants)

    Typical usage ratio

    • Ranges from 0.5–5 vol% as extractant in aqueous/organic two-phase systems, increased if target solute concentration is below threshold or for metals with low distribution coefficients.

    Downstream process integration

    • Introduced to extraction columns or stirred tank reactors, followed by separation via decantation, ultrafiltration, or anti-solvent precipitation for solute recovery.

    Final product types

    • Palladium, platinum, or rare-earth metal concentrates
    • Purified organic acid isolates for bioprocessing
    • Non-volatile ionic liquid-based green solvents for circuit board leaching

    4. Functional Monomer in Ion-Exchange Resin Production

    Resin producers incorporate this material as a specialty monomer to embed sulfonic acid and imidazolium groups directly onto crosslinked polymer beads, significantly increasing ion-exchange capacity and chemical durability for water treatment and specialized separation modules. The presence of a vinyl group enables direct copolymerization with styrene or DVB during bead formation.

    Industry compliance standards

    • NSF/ANSI 61 (Drinking Water System Components – Health Effects)
    • China Hygienic Standard for Drinking Water Treatment Chemicals (GB 18300-2001)
    • ISO 9001:2015 (Resin quality management systems)
    • FDA 21 CFR 173.25 (U.S. compliance for ion-exchange resins in food processing water)

    Typical usage ratio

    • 3–8 wt% in resin bead feed mixture, dependent on desired acid group density and mechanical bead strength; higher end for industrial deionization units.

    Downstream process integration

    • Added to the monomer mixture before emulsion or suspension polymerization, allowing for rigid and functional bead formation, followed by sieving and post-polymerization sulfonation (if required).

    Final product types

    • Strong-acid cation-exchange resins for boiler water treatment
    • Mixed-bed resins for semiconductor ultrapure water applications
    • Specialty polymer beads for pharmaceutical purification columns

    5. Modifier in Anti-Static Polymeric Coatings for Microelectronics

    Manufacturers of advanced anti-static coatings for semiconductor cleanrooms and electronics encapsulation utilize this compound to enhance surface charge dissipation and moisture compatibility. Its vinyl group allows chemical linkage to acrylate matrices, while the sulfonic acid improves conductivity and suppresses particulate adherence during and after curing, in line with stringent electronics process controls.

    Industry compliance standards

    • IPC-CC-830C (Qualification and Performance of Electrical Insulating Compounds for Electronics)
    • IEC 61340-5-1 (Protection of Electronic Devices from Electrostatic Phenomena)
    • RoHS Directive 2011/65/EU (Restriction of Hazardous Substances in electronics manufacturing)
    • GB/T 2423.17 (Testing anti-static performance for electronics coatings)

    Typical usage ratio

    • Typically 0.5–2 wt% incorporated into coating formulations; higher percentages for thick film or high humidity environments.

    Downstream process integration

    • Dispersed into prepolymer blends or introduced at the pigment grind stage, followed by UV or thermal curing on clean substrates.

    Final product types

    • Floor and wall anti-static coatings for electronics manufacturing cleanrooms
    • Encapsulation and conformal coatings for PCB protection
    • Electronic device casings with permanent static dissipation
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    Certification & Compliance
    More Introduction

    1-Propylsulfonic-3-Vinylimidazolium Chloride: Real-World Experience from the Manufacturer’s Lab

    The Chemical from the Core of the Lab

    We don’t often see a molecule spark as much conversation as 1-Propylsulfonic-3-Vinylimidazolium Chloride. During years of direct synthesis and real-world application testing, I’ve handled hundreds of ionic liquids and imidazolium derivatives. Some chemicals perform reliably but quietly, others grab attention with their versatility. This one, with its unique structure and functional groups, managed both. For those new to this material, we synthesize it under strict purity conditions and test every batch for moisture, residual solvents, and catalytic performance. The vinyl group, attached to the imidazolium ring, does more than earn it a place on spec sheets—it opens doors in polymer chemistry you don’t get with conventional ionic liquids. The propylsulfonic tail turns up the hydrophilicity, which we’ve seen let our partners experiment with water-rich processes without losing chemical consistency.

    Unique Build, Distinct Behavior

    As a direct manufacturer, the full life-cycle of this chloride salt plays out in front of us, from monomer feedstocks to pilot-scale couplings. Our process optimization stems from understanding the two catalytic faces of the compound: the imidazolium cation and sulfonic acid group. We learned early that this duality brings both acidity and ionic character, letting developers skip the juggling act of blending two separate catalyst types. The vinyl group—often overlooked—enables the molecule to participate directly in radical and addition polymerizations. In melt-state or solvent conditions, its ionic mobility gives it a performance edge over more traditional, non-functionalized imidazolium salts.

    What stands out in lab-testing is the consistent melting point—something our QC team values for reproducibility. Many customers report reliable behavior in aqueous and polar organic systems alike, with low volatility under moderate heating. No detectable foul odor, minimal discoloration, stable upon storage at ambient lab conditions.

    Applications We’ve Explored—and Where the Benefits Show Up

    Colleagues and research partners tell us they appreciate the way the sulfonic acid group shifts reactivity. Hydrogen-bonding networks in this material turn up strong; that often boosts catalytic activity in acid-catalyzed transformations. We’ve seen solid uptake in esterification and etherification protocols, and it doesn’t degrade or foam under the typical reaction cycles.

    Polymer chemists come to us looking to introduce functionality into chains without excessive use of copolymerization steps. The vinyl group on the imidazolium core lines up perfectly for free-radical or controlled polymerization methods, so end-users can build materials with attached ionic sites right into the backbone. Compared to non-vinyl imidazolium salts, customers typically report easier integration into hydrogels, membranes, or polyelectrolyte networks, without persistent bleed or leaching post-polymerization.

    The product finds a useful role in environmental separation technologies too. Ionic liquid-based extractions often struggle with selectivity; the sulfonic acid feature turns this weakness into strength. Experimental results and partner pilot programs have shown improved removal efficiency for organo-nitrogen or organosulfur compounds due to the strong ionic pairing.

    The Model We Provide

    Our standard production grade hovers around 99% minimum purity. This isn’t just a marketing promise—consistent feedback on NMR and elemental analysis from technical partners confirm tight batch-to-batch control. We manufacture and pack as a crystalline solid, often pale white to off-white, with moisture content under 0.3%. For larger scale users, custom batches can be prepared with melt-state or fine powder granulation, but our main production stays focused on laboratory-ready volumes and pilot-plant needs.

    How It’s Different from Competing Chemicals

    With many ionic liquids and imidazolium-based compounds hitting the market, it’s easy to overlook distinctions that matter in practice. You won’t get vinyl functionality on most off-the-shelf imidazolium salts—adding this group means the material doesn’t just dissolve or ion-exchange, it participates in the chemistry. During bench-scale polymerizations, the difference is clear: you don’t need external crosslinkers or post-modification, as the vinyl handle bonds right into the chain. Sulfonic-functionalized imidazolium chlorides are not rare, but adding this functionality with an attached vinyl group while retaining a manageable melting point is what separates this product from others built only for ionic conductivity.

    In catalysis, generic imidazoliums simply don’t show the same acidity or phase behavior—most can’t replace classic mineral acids in industrial transformations without process tweaks. The molecule we produce, with its propylsulfonic group, shows real acid catalysis potential in esterifications that usually demand added mineral acids or solid acid resins. Our formulation has routinely saved end-users from waste acid neutralizations and downstream filtration issues.

    Physically, some ionic liquids struggle with water uptake, discoloration, or slow deterioration. Our QC team tracks degradation under both ambient and sealed conditions, and we monitor for the oxidative stability customers have flagged as a concern. We’ve documented storage at room temperature for six months with no detectable hydrolysis, and third-party labs have confirmed shelf-stability that beats most similar sulfonic-functionalized peers.

    Using the Compound—Process Insights from Real Trials

    As a manufacturer, we’re responsible for more than a certificate of analysis—we run our own bench-scale application trials. When lab partners prepare polymer membranes with this chloride, they report homogeneous mixing and incorporation, with no need for pre-activation treatments. We’ve zeroed in on pH stability after several customers highlighted drift in competitive acidic ionic liquids. The propylsulfonic acid remains protonated under highly acidic conditions and doesn’t noticeably hydrolyze in the presence of wet alcohols, ketones, or water, which speaks to synthesis quality and purification method.

    Performance in catalysis has gained attention. In transesterification protocols, the catalytic activity stays consistent for three or more cycles, with minimal leaching reported after repeated use. Partners running synthesis on silica or polymer supports note solid immobilization, with no visible crystallization or performance fade-off over dozens of batch runs. In contrast, non-vinyl sulfonic imidazolium salts often either leach off or form sticky residues, which pushes up separation and cleaning costs.

    Our plant opts for batch over continuous synthesis. This gives us tighter process adjustment and finer purity control. Several of our technical team members have backgrounds in both organic and process chemistry, letting us iterate adjustments until the color, melting point, and activity line up with QA & customer standards. We maintain full traceability, able to trace impurity origins back to upstream feedstocks. When customers do discover an issue, we can usually trace it to specific solvent lots or storage conditions, not repeated process failings.

    Practical Considerations in Handling and Storage

    In manufacturing, every small detail can affect large-batch reproducibility. We never ship until the sample meets spectral, elemental, and water content requirements. Customers report the solid dissolves readily in water, alcohols, and mild polar aprotic solvents. In comparison, generic imidazolium salts often suffer agglomeration or incomplete wetting. No irritating odor or notable dusting, which eases handling in both automated feeders and manual weighing stations.

    We pack in air-tight, high-density polyethylene containers, paying close attention to moisture control—excess humidity can interfere with not only measurement but polymerization results. Competing materials shipped in foil packs or loose bags have triggered complaints about caking and discoloration. Long storage in our own facility hasn’t caused any caramelization or sulfurous odor, indicating both chemical and microbial stability.

    Spill recovery remains straightforward; no toxic fume release or viscosity spikes, so minor incidents on benchtops cause little trouble—just a quick solvent wipe-down or saline wash. While no chemical is risk-free, our product’s low volatility means users rarely experience transient exposure hazards, even when processing multi-kilogram quantities.

    Regulatory and Environmental Performance on the Shop Floor

    Customers often ask about environmental performance, particularly regarding persistence and disposal. In-house testing and consultation with academic partners spotlight relative bio-persistence and aquatic toxicity compared to both phosphonium and pyridinium-based ionic liquids. The chloride counterion, the sulfonate chain, and the imidazolium core all influence breakdown. Waste streams after catalysis rarely include any detectable micro-contaminants after water and mild acid washes. In combustion scenarios, no obscure byproducts or persistent organohalogens have been flagged. Our own plant’s wastewater consistently tests under all local effluent standards.

    Unlike classic acids or halide salts, our material hasn’t triggered pitting or corrosion in stainless reactors, based on years of equipment life monitoring. No unusual maintenance needs have been reported due to buildup. This is not always true for purely sulfonic or halide-rich ionic mixtures, where deposits and etching force additional downtime. Safety team audits confirm storage and transfer processes routinely meet all occupational exposure limits currently regulated.

    Feedback from the Field—Direct and Candid

    We ask users for more than a procurement report. Over thousands of kilograms supplied, we’ve been told that chemists and engineers alike favor the reagent’s dual acidity and polymer compatibility. Polymer labs cite fast, even dispersion in both pilot and plant reactors. Catalysis teams notice reaction times drop when switching from basic imidazolium analogs, and most report improved recovery of end materials with fewer purification cycles.

    Some customers tried blending in this chloride with commodity ionic liquids, attempting to cut costs or increase conductivity. Their lab notes show this doesn’t always bring the intended benefits—the unique reactivity gets diluted, making polymerization less predictable. Pure use gives more consistent catalysis and functional incorporation.

    Green chemistry teams talk about reduced neutralization waste streams. For several water-intensive synthesis lines, incorporating this product shaved full days off resin washing and filtration, thanks to its efficient catalytic role and cleaner reactions. One pilot plant halved its caustic neutralization load in block-copolymer synthesis simply by making the switch, which was confirmed by hard cost data in their quarterly report to us.

    Challenges get reported, too. Some applications—especially those requiring extremely low chloride content or strictly non-ionic systems—haven’t benefited. In these cases, customers stuck with alternative acid catalysts or chose a different counterion. We aren’t shy about acknowledging such feedback: not every property lines up with every possible use-case. That kind of field knowledge informs our process development and guides future product design.

    Production Choices that Support Better Chemistry

    Some users want technical details about our synthesis, others focus on results. In our own pilot plant, we react the key precursors in photochemically neutral surroundings to preserve the vinyl functionality. We run repeated crystallizations for fine control over trace organics and maintain clean-room handling for final steps. Each batch gets run through our IR, 1H NMR, and total sulfur checks. Leaving these steps out has caused off-color batches in the past—a mistake we don’t allow again.

    A deep dive into historic batch logs shows our run-to-run variability has dropped below 0.4% since adopting full-spectrum QA. With a root-cause database going back years, we can trace any impurity spike or odd performance to equipment or batch chemistry, not random error. Running large equipment at low throughput costs more, but it’s paid off in user confidence and repeat business.

    Why Direct Manufacturing Matters

    Supplying directly cuts out layers of confusion, so our chemists talk straight with your development leads. It means real-time adjustments and no lag for feedback on outlier results. We have no reason to represent specs or performance that won’t hold up under scrutiny, because we’re the ones making and backing every batch. Manufacturers, unlike traders, know the full physical and chemical fingerprint of each run, so we don’t rely on someone else’s word or warranty.

    Production choices—from solvent grade to water removal steps—might sound simple, but the difference shows up in months of storage and in the consistency of reaction outcomes. Whenever someone questions batch purity or performance, we bring forward lab histories, not generic assurances. That transparency helps build trust with teams scaling up from grams to kilograms to tons.

    Real Chemistry, Not Commodity

    As a direct manufacturer, we don’t cast this as a magic bullet for all chemistry. But everyday work at the bench and in the plant says it beats standard ionic liquids each time polymerizable or strongly acidic functionality is a must. The vinyl group makes real functional materials possible in a single synthetic step. The propylsulfonic chain increases compatibility and boosts reactivity. The chloride counterion brings both solubility and handling ease.

    We keep collecting hard data, process histories, and user feedback to refine production. The more time spent making and using this compound, the clearer its strengths and limitations become. For anyone looking to build new functional polymers, boost green acid-catalyzed reactions, or streamline environmental separation, 1-Propylsulfonic-3-Vinylimidazolium Chloride supplies a combination of properties not found in basic imidazolium or commodity ionic liquids. True understanding only comes from production, application, and direct engagement—something every real chemical producer knows.