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1-Dodecyl-3-Methylimidazolium Chloride

    • Product Name 1-Dodecyl-3-Methylimidazolium Chloride
    • Alias [C12mim]Cl
    • Einecs 432-370-5
    • 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

    757484

    Cas Number 24155-42-8
    Molecular Formula C16H33ClN2
    Molecular Weight 288.91 g/mol
    Appearance White to off-white powder
    Melting Point 65-70°C
    Solubility In Water Soluble
    Purity ≥98%
    Ionic Liquid Type Imidazolium-based
    Density 0.99 g/cm3 (at 25°C)
    Storage Condition Store at room temperature, in a tightly closed container
    Ph 1 Solution 5.5-7.5 (approximate)
    Odor Odorless
    Synonyms C12mimCl; Dodecylmethylimidazolium chloride

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

    Packing & Storage
    Packing A sealed, amber glass bottle containing 100 grams of 1-Dodecyl-3-Methylimidazolium Chloride, labeled with safety and product information.
    Shipping **1-Dodecyl-3-Methylimidazolium Chloride** is shipped in tightly sealed, chemically-resistant containers to prevent moisture exposure and contamination. Packages are clearly labeled and handled according to applicable chemical transport regulations. Standard shipping is via ground or air, with appropriate safety documentation included. Store in a cool, dry place upon receipt.
    Storage 1-Dodecyl-3-Methylimidazolium Chloride should be stored in a tightly sealed container in a cool, dry, and well-ventilated area, away from moisture, heat, and incompatible substances such as strong oxidizers. It should be kept out of direct sunlight and protected from physical damage. Ensure appropriate labeling, and store away from food and drink. Use proper personal protective equipment (PPE) when handling.
    Application of 1-Dodecyl-3-Methylimidazolium Chloride

    Applications of 1-Dodecyl-3-Methylimidazolium Chloride in Industrial Manufacturing

    As a direct manufacturer of 1-Dodecyl-3-Methylimidazolium Chloride, we supply this specialty imidazolium-based ionic liquid to industrial customers focused on formulated chemistry and advanced materials manufacturing. Below we outline key downstream application scenarios based on established global usage patterns, each covering sector-specific standards, dosage practices, process integration points, and representative end products.

    1. Cellulose Dissolution and Processing for Specialty Fibers

    Major specialty fiber producers leverage this imidazolium salt to dissolve cellulose under mild thermal conditions, avoiding direct use of aggressive solvents. Its strong hydrogen-bond disruption capacity allows for precise control in viscose, lyocell, and other regenerated cellulose production workflows. Fiber spinning operations integrating ionic liquid-mediated dissolution target high-purity, consistent yield, and minimized residuals in finished films and continuous fibers.

    Industry compliance standards

    • ISO 9001:2015 Quality Management Systems
    • OEKO-TEX® Standard 100 for textile chemical safety
    • EU REACH chemical registration provisions for process aids
    • ZDHC (Zero Discharge of Hazardous Chemicals) Manufacturing Restricted Substances List

    Typical usage ratio

    • 20–40 wt% relative to dry cellulose, subject to adjustment for intrinsic viscosity and required dissolution rate

    Downstream process integration

    • Direct addition to cellulose pre-treatment reactors following initial pulp dispersion and prior to secondary solubilization or spinning bath feed

    Final product types

    • Lyocell fibers for performance textiles
    • Regenerated cellulose films (e.g., for specialty packaging)
    • High-purity microcrystalline cellulose for pharmaceutical/food applications
    • Technical yarns requiring low extractable residues

    2. Surfactant and Emulsifier in Enhanced Oil Recovery (EOR) Formulations

    Oilfield chemical formulators use the long hydrocarbon chain and ionic interface of this material to develop EOR blends that improve interfacial tension modification and microemulsion stability in tertiary recovery wells. These unique formulations operate in high-salinity, elevated-temperature reservoirs, requiring consistent ionic liquid purity and reproducibility of batch quality for regulatory and process compliance.

    Industry compliance standards

    • API RP 19C (Recommended Practices for Chemical EOR)
    • OCMA (Oil Companies Materials Association) and ASTM D5287 crude compatibility guidance
    • EU REACH Annex XVII, restriction entries related to environmental discharge

    Typical usage ratio

    • 0.2–1.0 wt% in total injection fluid; field engineers determine dose based on brine composition and crude properties

    Downstream process integration

    • Inline blending with water-flood or polymer-flood agents before downhole injection during tertiary recovery campaign setup

    Final product types

    • Formulated chemical EOR packages shipped to oilfield operators
    • Custom surfactant concentrates for on-site brine dilution
    • Ready-to-use injection fluids for mature oil reservoir stimulation

    3. Phase Transfer Catalyst in Fine Chemical Synthesis

    Producers of advanced specialty intermediates select dodecyl-methylimidazolium chloride as an effective phase transfer catalyst, especially in nucleophilic substitution and alkylation reactions where improved yields and selectivity are critical. The ionic liquid enables successful catalysis across biphasic organic-aqueous systems, reducing side reactions while maintaining product purity within strict specifications demanded by downstream active ingredient markets.

    Industry compliance standards

    • GMP ICH Q7A for pharmaceutical ingredient manufacturing
    • ISO 14001 for environmental management in chemical synthesis
    • EU Regulation (EC) No 1223/2009 for cosmetic ingredient safety (where relevant)

    Typical usage ratio

    • 0.5–3 mol% relative to limiting substrate; actual charge determined by hydrophobic substrate ratio and batch scale

    Downstream process integration

    • Dispersion into reaction mixtures during charging of aqueous-organic phase systems, preceding base or nucleophile introduction

    Final product types

    • Specialty pharmaceutical intermediates
    • Custom agrochemical actives and protected intermediates
    • Cosmetic grade quaternary ammonium compounds

    4. Antistatic Agent in Polyolefin Masterbatch Production

    Engineering plastics compounding facilities incorporate dodecyl-methylimidazolium chloride into masterbatches for polyolefins, targeting durable static dissipation in consumer and industrial polymers. The ionic structure delivers antistatic properties that meet permanent or semi-permanent requirements, as verified in surface resistivity and migration rate testing post-extrusion. Compounding requires careful calibration of charge to maintain polymer transparency and mechanical performance.

    Industry compliance standards

    • FDA CFR 21 §177.1520 for additives in olefin polymers (where used in food contact)
    • UL 94 flammability standards for electrical and electronics applications
    • RoHS 2011/65/EU for electrical/E&E polymers

    Typical usage ratio

    • 0.1–0.5 wt% in final resin; dosage varies by target surface resistivity and polymer base (PP, PE, etc.)

    Downstream process integration

    • Premix with base resin in twin-screw extrusion prior to pelletization and let-down by end processor

    Final product types

    • Antistatic masterbatches for cable sheathing
    • Polyolefin films for electronics packaging
    • Plastic components for consumer appliances requiring ESD control

    5. Corrosion Inhibition Additive in Water-Based Metalworking Fluids

    Metalworking fluid formulators employ dodecyl-imidazolium chloride as a corrosion inhibition ingredient, capitalizing on its high surface activity and film-forming capabilities on ferrous and non-ferrous substrates. The ionic liquid functions in coolant blends for cutting, grinding, and machining, where controlled release protects workpieces and machine surfaces from corrosion even under high-load and recirculated systems.

    Industry compliance standards

    • ASTM D4627 for evaluating corrosion protection of water-based fluids
    • ISO 6743-13:2010 for classification of metalworking fluids
    • REACH Annex XIV for approval of use in industrial lubricants in EU

    Typical usage ratio

    • 0.05–0.3 wt% in concentrate; adjusted higher for systems with aggressive water chemistries or elevated temperature operating cycles

    Downstream process integration

    • Batch blended into fluid base stock, followed by emulsification and dosage checks prior to packaging as ready-to-dilute coolant

    Final product types

    • Concentrated water-miscible metalworking coolants
    • Premixed anti-corrosion cutting fluids
    • Maintenance fluids for CNC and high-speed machining equipment

    6. Electrolyte Additive in Supercapacitor and Battery Manufacturing

    Manufacturers of supercapacitors and next-generation batteries utilize this ionic liquid to enhance electrolyte conductivity, widen operative voltage windows, and improve long-term cycle stability. The chloride anion and hydrophobic cation combination mitigates gas evolution and electrode degradation, supporting high-performance energy storage devices. Quality assurance relies on impurity profiling and ionic purity throughout each production campaign.

    Industry compliance standards

    • IEC 62660-2 performance and reliability requirements for lithium-ion batteries
    • RoHS and REACH substance regulations for finished electrical goods
    • QC/T 743 (China automotive industry standard for supercapacitor modules)

    Typical usage ratio

    • 10–30 vol% of total electrolyte blend; specific ratio selected based on cell architecture and operational temperature profile

    Downstream process integration

    • Mixed with other organic or aqueous electrolyte solvents during electrolyte formulation prior to cell filling or electrode wetting

    Final product types

    • Electrolyte packs for supercapacitor banks
    • Commercial lithium-ion and hybrid-ion secondary batteries
    • High-voltage industrial capacitors for UPS and grid stabilization
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    Certification & Compliance
    More Introduction

    1-Dodecyl-3-Methylimidazolium Chloride: Real-World Experience From the Manufacturer's Perspective

    A Straightforward Introduction to Our Ionic Liquid

    Crafting specialty chemicals often means stepping into lesser-known territory, and in our case, we’ve watched 1-Dodecyl-3-Methylimidazolium Chloride, known among researchers as [C12mim]Cl, become a workhorse for many advanced applications. Sitting within the imidazolium-based ionic liquid family, this compound delivers something we haven’t encountered as consistently elsewhere: a balance of surface activity, strong solubility character, and thermal stability.

    On the shop floor, we blend this quaternary ammonium salt under strictly controlled anhydrous conditions. We check every batch following synthesis and purification to capture even faint impurities and residual water, since these subtle changes impact downstream performance. It’s colorless to pale yellow in its purest form, crystalline in texture at room temperature, and easily dissolves in a range of polar solvents, including water, DMSO, and methanol.

    Model, Specifications, and What Sets It Apart

    Our main model covers industrial-grade [C12mim]Cl with >98% purity, and we offer analytical reports on residual sodium, chloride, and common organic contaminants. Shelf stability depends upon packaging and storage. Sealed, moisture-free environments preserve its flow and handling properties even after several months. If any trace excess water appears, the salt can clump, so we outfit our packaging lines with desiccant integrations and vacuum-sealed bags when required.

    Unlike short-chain imidazolium salts such as 1-Butyl-3-Methylimidazolium Chloride, the dodecyl (C12) tail grants pronounced amphiphilic character. This structure improves its surface activity and allows it to act both as a cationic surfactant and ionic liquid, bridging organic–aqueous interfaces that shorter chains cannot. The long hydrocarbon chain brings stronger micelle formation, low critical micelle concentrations, and even mild antimicrobial effects under certain test conditions. In our experience, this means formulations that require extended-chain surfactancy—say, in emulsions or phase transfer systems—perform more predictably.

    We batch test at different points in the year to account for seasonal changes in ambient humidity and supply quality. Any deviation from purity shows up not only in color but also in melting point and viscosity checks. We’ve learned this level of care during production and packing is critical since researchers and industrial users alike have sensitive downstream processes, whether as a solvent platform, catalyst base, or in more specialized nanomaterial synthesis.

    Major Uses and Industry Insights

    Chemical engineers and R&D teams use 1-Dodecyl-3-Methylimidazolium Chloride for more than just the ionic liquid label suggests. The compound’s long alkyl chain increases hydrophobic zone formation in solution, making it indispensable where other imidazolium salts fall short.

    Industrial customers lean on it for:

    We keep hearing requests for documentation about biocidal and toxicity information, and our technical team works closely with academic groups and regulators to monitor the latest findings. Imidazolium ionic liquids have been scrutinized for aquatic toxicity; the C12 variant, as with similar amphiphilic cations, has demonstrated measurable impacts in direct exposure toxicity studies. We provide our partners with breakdown data and guidance on safe disposal practices based on peer-reviewed publications and our own lab-scale degradation studies.

    How [C12mim]Cl Performs Versus Other Imidazolium Salts

    Imidazolium-based ionic liquids all share a similar cation, but the side-chain length and halide counterion bring varied behaviors. With 1-Butyl-3-methylimidazolium chloride, most users note easier room-temperature handling and lower viscosity. Longer chains, like our dodecyl version, form stronger hydrophobic domains and act as more efficient surfactants—outperforming short-tail types in solubilizing organic compounds and templating porous frameworks.

    We’ve made direct side-by-side batch comparisons: under identical pH, temperature, and solvent conditions, [C12mim]Cl builds more robust micellar networks, allowing higher oil-in-water emulsification and better encapsulation of hydrophobic substances. This influences not only laboratory processes but also scale-up plans, where breakage of the micelle phase or coalescence can throw a wrench in processing and downstream recovery.

    Counterion choice affects physical properties as well. Chloride, as the anion, offers good water solubility and a lower melting point compared to [C12mim]Br or other halide variants. We monitor performance differences constantly: higher salt concentrations can precipitate in certain solvent systems, so solubility data for your target matrix is just as crucial as pH or buffer compatibility.

    Technical Challenges and Practical Solutions

    Transitioning from lab synthesis to full-scale manufacturing has taught us important production lessons. The long dodecyl chain, while beneficial in performance, can complicate reaction clean-up and column purification. We’ve moved to continuous flow drying and column fractionation that reduces side-products and batch reprocessing. Our hands-on experience leads us to scan every output for trace product degradation—sometimes triggered by residual acids or salts left over from earlier reaction steps. Preventing this means regular recalibration of in-process sensors and strict adherence to validated workflows.

    On the logistical side, bulkier solid forms of [C12mim]Cl can agglomerate under damp conditions—a common problem with cationic surfactants packed in standard bags. To counter that, we use containers lined with metallic foils and thick barrier films, and keep warehouse dehumidifiers running year-round. These steps help preserve free-flowing crystalline product, even in tropical or highly variable warehouse climates.

    Transportation of this product requires clear hazard labeling. Although its toxicity sits far below heavy metal salts or classic long-chain quat disinfectants, its amphiphilic and ionic character mean spills and leaks in transport could pose local aquatic risks. We work with logistics providers who understand chemical handling and build packaging that resists puncture and moisture ingress.

    User Feedback and Real-World Workarounds

    Many of our long-term customers come from startup labs and process development teams. They ask for technical tweaks: requests for lower sodium levels, tighter melting point specs, or even custom blending with other surfactants and ionic liquids. Fulfilling these requires a versatile plant setup and responsive production switching.

    Some users report increased viscosity in their final product when using [C12mim]Cl as a driver for emulsification—a natural result of the long alkyl group. Our support team addresses these reports by providing blending and dilution guidance, drawing from lab data and direct pilot trial observations. Scaling up ionic liquid systems nearly always poses new hurdles, and not every adjustment has a textbook solution. Close feedback loops from testing sites allow us to recommend incremental process changes.

    We receive regular questions about batch-to-batch consistency. That’s a challenge for any ionic liquid manufacturer, especially as customers push process boundaries. Each run demands attention to detail in both synthesis and storage phases. Small uncontrolled process shifts (subtle pH, trace co-solvents, or even variance in starting amine purity) can affect the surface tension performance and require corrective blending post-synthesis.

    Working With [C12mim]Cl: Lessons From The Floor

    Operators in our production hall see the variability first-hand—sometimes bulk batches arrive at filling stations with the right melting range but unexpected clumping. Our solution has been dividing solid product into small, foil-lined packets in high-humidity summer months, and shifting back to bulk drums only when room dehumidification hits optimal targets. We also monitor employee safety closely; although this compound is not acutely toxic, direct skin and eye exposure causes irritation and dermal drying. Standard PPE suffices, and we train staff not to cut corners, even during peak production rush.

    Regular oven-drying and pre-mixing tests ensure the delivered product meets customer specs, even in the face of global supply chain inconsistencies. Each technical staffer signs off on quality and lot traceability, and we keep records of every deviation, using them to tune early-stage process controls for following runs.

    Research Horizons and Collaboration

    Lab partnerships drive continuous improvement in both product and process. We support academic research groups testing [C12mim]Cl in environmental remediation, solvent-free organic catalysis, and next-generation electrolytes. The compound’s ability to structure water–organic interfaces underpins broad interest across green chemistry and renewable materials research. Universities share their peer-reviewed findings with us, and in turn, we develop case studies and process guidelines rooted in quantitative lab outcomes.

    We see steady demand from teams working on sustainable extraction processes. Here, the amphiphilic profile of [C12mim]Cl enables mild, tunable solvation—no volatile organic solvents, lower reaction temperatures, and simpler downstream recovery. We often hear from our clients about the value of running comparative solvent screens, and we offer technical support to aid rational solvent selection for each specific substrate, rather than relying on generic solvent lists.

    Our position as a manufacturer provides us deeper insights into which performance variables are controllable and which require material redesign. By collaborating with specialists in catalysis, electrochemistry, and advanced materials, we help transfer lab-scale know-how into scalable industrial practices. Air-sensitive systems, rare-earth processing, and surface treatment operations each reveal new demands, keeping product development cycles focused and grounded in actual process output.

    Responsible Production and Environmental Impact

    As fabricators of specialty ionic liquids, environmental and workplace safety sit alongside technical quality. We’ve invested in closed-system transfer lines, in-house wastewater quality monitoring, and solvent recovery setups. Reliable data from both plant output and third-party waste audits confirms that process water and spent solvents show trace ionic residue far below local discharge standards after treatment. Our R&D teams are exploring further improvements in green synthesis, including biobased precursor routes and more energy-efficient purification stages.

    We recognize ongoing debate regarding the persistence and toxicity of imidazolium ionic liquids. Our own tests mirror literature studies showing moderate acute aquatic toxicity and slow abiotic degradation under typical wastewater treatment conditions. In response, we keep both staff and customers updated with published toxicological profiles, encourage best practices in lab-scale waste capture, and partner with external evaluators to improve environmental fate modeling. Building toward closed-loop recycling and cradle-to-cradle usage remains an active area for product stewardship.

    Bulk users in extraction or cleaning are especially concerned with minimizing aqueous runoff. We advise direct waste recovery and neutralization, typically through activated carbon filters or dilution to benign levels prior to final disposal. Crew training stresses spill prevention, rapid clean-up, and protective handling, ensuring both product quality and user health remain protected.

    Continued Evolution: Market Trends and Manufacturer Response

    Demand for 1-Dodecyl-3-Methylimidazolium Chloride grows alongside the trend toward multifunctional, eco-friendlier alternatives in material science and synthesis. The ionic liquid’s versatility is reflected in requests from pharmaceutical process optimization, battery research, and even personal care product formulation.

    We see competitors offering similar materials—sometimes at lower initial cost—but we remain committed to rigorous purity, batch consistency, and responsive after-sales support. Speed of delivery and the availability of custom pack sizes are now valued as highly as base performance, because customers expect flexible, low-waste supply chains capable of fast switching between project requirements. We’ve built our reputation upon meeting short lead times and providing customers with direct access to our technical experts.

    Customer feedback continues to drive improvements. Whether it’s a tweak to starting materials, adjustments in the post-synthesis drying phase, or new application guides based on field observations, we treat every piece of input as a foundation for ongoing process refinement. As technology and regulatory standards evolve, we stay prepared to reshape our offering while holding to the same standards of quality and safety that set our material apart in the first place.

    In Summary: The Manufacturer’s View on 1-Dodecyl-3-Methylimidazolium Chloride

    Manufacturing 1-Dodecyl-3-Methylimidazolium Chloride draws together process experience, technical knowledge, and a commitment to quality control. From raw materials selection right through to customer feedback analysis, our work with [C12mim]Cl represents continuous learning. Unique among imidazolium salts, its amphiphilic properties let customers bridge demanding technical gaps in surfactant operation, catalysis, extraction, and more.

    Our in-house chemists, plant engineers, and front-line operators all contribute to an evolving understanding of best practice. We continue investing in cleaner, safer, and more sustainable methods to support not only customer projects but the communities and environments linked to our operations. For every new customer inquiry, we approach the task with hard-won insight—and a willingness to adapt as technology and markets shift.

    We remain open to collaboration and transparent about the material’s challenges. By treating each new application as a shared learning opportunity, we help users squeeze the most value out of 1-Dodecyl-3-Methylimidazolium Chloride and push the boundaries of what ionic liquids can achieve.