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HS Code |
422330 |
| Product Name | 1-Dodecyl-3-Methylimidazolium Iodinide |
| Chemical Formula | C16H31IN2 |
| Appearance | White to off-white solid |
| Melting Point | Approximately 45-55°C |
| Boiling Point | Decomposes before boiling |
| Solubility In Water | Soluble |
| Cas Number | 342573-75-1 |
| Storage Conditions | Store at room temperature, away from moisture |
| Density | 1.11 g/cm³ |
| Purity | Typically ≥98% |
| Odor | Odorless |
| Stability | Stable under recommended storage conditions |
| Synonyms | C12MIM Iodide |
As an accredited 1-Dodecyl-3-Methylimidazolium Iodinide factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle, 100g, tightly sealed with screw cap and tamper-evident seal. Clearly labeled with chemical name, CAS, and hazard warnings. |
| Shipping | 1-Dodecyl-3-Methylimidazolium Iodinide is shipped in tightly sealed containers, protected from moisture and light, and labeled according to regulatory guidelines. During transit, it must be stored in a cool, dry place and handled with care as a chemical substance. Ensure compliance with all local and international shipping regulations. |
| Storage | 1-Dodecyl-3-methylimidazolium iodinide should be stored in a tightly sealed container, protected from light, moisture, and air. Keep it in a dry, cool, and well-ventilated area, away from incompatible substances such as strong oxidizers. Label the container clearly and store at room temperature or as recommended by the supplier, following all relevant safety and chemical storage guidelines. |
Applications of 1-Dodecyl-3-Methylimidazolium Iodinide in Industrial ManufacturingAs an established producer of 1-Dodecyl-3-Methylimidazolium Iodinide, we supply this functional ionic liquid to key industrial customers across several specialized sectors. The following application breakdown outlines real downstream use cases, specifying compliance requirements, application ratios, processing steps, and common end-products. Clear structuring and technical information support reliable partner integration. 1. Organic Electronics: Conducting Ink FormulationMajor electronic device manufacturers use 1-Dodecyl-3-Methylimidazolium Iodinide as a dopant and ion transport agent in the formulation of conductive inks. It efficiently enhances ionic conductivity and inkjet printing reliability for organic semiconductors and light-emitting devices. Production processes require precise control over humidity and particles, as well as controlled blending with polymer matrices for stable deposition quality. Industry compliance standards
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2. Dye-Sensitized Solar Cells (DSSC) Electrolyte SystemsLeading solar module OEMs incorporate this ionic liquid as an iodine source and charge-transfer mediator in DSSC electrolytes. The compound supports stable triiodide/iodide redox cycling, while enabling low-volatility, high-thermal-stability cell assemblies. Material purity and controlled moisture are critical for electrolyte performance in this market. Industry compliance standards
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3. Phase-Transfer Catalysis in Organic SynthesisMajor fine chemical and pharmaceutical manufacturers utilize this imidazolium salt as a phase-transfer catalyst (PTC) to promote nucleophilic substitution and oxidation reactions. The long alkyl chain imparts efficient interface transfer while the iodide anion supports rapid reaction turnover, especially in halide exchange processes. Reactant purity and aqueous/organic phase ratios are stringently managed throughout manufacturing flows. Industry compliance standards
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4. Antimicrobial Additive in High-Performance Polymer CompositesEngineered plastics and specialty composite manufacturers employ this material as an antimicrobial/antifungal additive in polyolefins and polyurethane systems. The organic cation segment disrupts microbial membranes, while the iodide component enhances biocidal spectrum. Careful masterbatch dispersion and compounding temperature controls prevent decomposition during extrusion or molding. Industry compliance standards
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Years of working with imidazolium-based ionic liquids in our manufacturing plant have shown us how each new compound can shift the boundary of what researchers and engineers accomplish. Our 1-Dodecyl-3-Methylimidazolium Iodinide delivers a distinct mix of stability, low volatility, and reliable solubility, giving chemists a unique edge in both exploratory and routine settings. Unlike traditional salts or basic solvents, this product joins long-chain dodecyl chemistry with the trusted imidazolium platform, paired with the iodide counterion, which opens doors to applications where halide coordination or transfer properties matter.
As an ionic liquid, 1-Dodecyl-3-Methylimidazolium Iodinide steps up to tasks that push conventional solvents beyond their comfort zone. The product runs as a clear to pale-yellow liquid at room temperature. That matters for anyone weary from fighting with solid handling or high melting points. Chemists running demanding syntheses, extraction projects, or catalysis experiments tell us that a liquid phase broadens compatibility and cuts waste streams from solid solvent recovery.
We mark each batch with a traceable lot number and track metrics like water content, halide purity, and NMR-confirmed structure. Routine production covers multiple scales—grams for specialty R&D, kilograms or more for ongoing formulation contracts. After each batch, we review not only purity but also functionality, often running internal application checks so your team sees similar performance regardless of the batch.
Our formulation keeps water content low, because excess water in ionic liquids throws off phase behavior and can wreck sensitive organic reactions or electrochemical measurements. Measured iodide level aligns with the stoichiometry, so you're not left guessing whether unreacted halide has lingered from synthesis. Clarity counts, too—visual checks and UV spectroscopy highlight even small contamination, which isn’t always obvious in routine titrations.
With longer alkyl chains, like dodecyl in this compound, the ionic liquid's hydrophobicity increases compared with shorter imidazolium variants. Practically speaking, this means you separate organic and aqueous phases more easily and avoid the hassle of repeated washes to chase down every last trace of ionic liquid from your product layer. We see the value in these small details because they keep post-reaction cleanups and downstream processing under control.
Laboratory groups and industrial partners rely on 1-Dodecyl-3-Methylimidazolium Iodinide in several well-established applications. In organic chemistry, the iodide anion plays a role as a nucleophile or halide source in transformations where other halides—like chloride or bromide—are less effective. Users running SN2 alkylation or halogen exchange reactions report faster conversions and cleaner product profiles with our compound compared with using methylimidazolium chloride or bromide forms.
Electrochemistry is another sector where this product stands out. The long alkyl chain increases viscosity modestly, but still supports free ion movement, supporting studies on redox couples, electrodeposition, and ionic transport measurements at moderate to elevated temperatures. In solar cell innovation, groups seeking durable electrolytes value the thermal stability of dodecylimidazolium iodide—especially under prolonged illumination and cycling.
Colleagues sometimes ask whether a switch from butyl or hexyl imidazolium to dodecyl affects more than just solubility. The answer, based on our in-house work and customer feedback, is that longer chains add hydrophobicity and reduce volatility. This change yields clear benefits for extractions, separations, and any process where phase splits save time and solvent. In contrast, methylimidazolium or ethylimidazolium with iodide may remain partially water-miscible, complicating recovery.
We see stronger attraction between dodecyl chains, yielding more robust layering at interface zones. For industrial separation setups, this means handling larger throughputs with cleaner splits, even when temperature fluctuates by several degrees. That same effect becomes critical in biphasic catalysis, where a stable ionic liquid layer supports phase transfer without persistent emulsions.
Switching from iodide to chloride drastically changes how the product interfaces with reagents and catalysts. Chloride shows stronger binding to many transition metals, which can inhibit some catalytic cycles, while iodide can accelerate oxidative addition steps and enable milder reaction conditions. Not every process benefits from iodide, but for palladium-catalyzed couplings or alkylations, those running the chemistry in-house routinely report higher yields with our dodecyl-imidazolium iodide than they see with the chloride analog.
Making this compound means managing risks tied to moisture, light exposure, and oxygen ingress. We pack every order in amber containers with airtight seals, based not just on shelf-life studies, but on experiments where samples stored outside guideline conditions rapidly yellowed or built up trace acid content. No-sweat packaging matters if users must store the liquid for weeks or months before use.
Storage practices trace back to our own experience—a lesson learned from early customer returns where repackaged samples suffered from high water absorption. We now double-seal every container and provide extra desiccant when shipping to humid climates. After these changes, customer complaints about instability dropped to nearly zero.
The product's physical state means less weighing and no battle with clumpy, electrostatically charged powders. If your workspace handles dozens of liquid transfers daily, small improvements in flow and dispensing help manage time and cut operator errors. The main bottle’s pour spout and viscosity at room temperature make dispensing directly into flasks straightforward. For automated setups, colleagues find that peristaltic and syringe pumps run cleanly—with fewer blockages compared with denser ionic liquids.
Disposal becomes less complicated than with halogenated organic solvents because the ionic nature slows volatility and reduces atmospheric emissions. In heavily regulated laboratories, staff report that waste management teams require fewer air-quality checks, and fume hood filtration units last longer between maintenance cycles.
Environmental responsibility takes more than claims about "greener solvents." We run our facility with a closed-loop water and solvent recovery system wherever possible. Ionic liquids, thanks to their negligible vapor pressure, do not contribute to lab air hazards that concern both staff and regulatory inspections. Routine internal studies measure VOC releases and confirm that our ionic liquid stocks, including this dodecyl iodide model, keep exposure levels below detection limits, even during handling and open transfers.
We regularly send samples for third-party toxicity screening to assess aquatic and soil persistence. These long-chain imidazolium salts show lower acute toxicity to local indicator species than many common organic solvents. Yet, persistence in water can become an issue, so we invest in supporting users with best practices for collection, neutralization, and recycling. Some industrial users have developed pilot programs for reclaiming spent ionic liquids through filtration and re-iodination, keeping resource use in check while shrinking their downstream environmental liabilities.
The world’s regulatory landscape keeps shifting, especially around specialty chemicals. Our customers in life sciences, electronics, and specialty materials require not just safety data sheets but also full traceability on precursor sourcing down to supplier declarations on restricted substances. Every bottle ships with a batch trace report including precursor lot numbers and third-party test results for halogen, metal, and organic impurity content.
Strict quality standards lead us to keep separate lines between dodecyl imidazolium iodide and other halide variants. Cross-contamination in ionic liquids is nearly invisible to routine in-lab analysis, so we enforce equipment cleaning, air scrubbing, and small-batch test runs when switching feedstocks. Several industry audits area customers have conducted have resulted in process corrections and technology upgrades—improvements that benefit all users by raising batch reliability year over year.
Feedback from laboratories worldwide has proven invaluable for tuning future formulations. We worked with synthetic chemists in Europe refining monomer coupling reactions, adjusting halide ratios and post-synthesis purification steps to achieve more consistent reaction times and higher selectivity. After implementing fractional crystallization and improved filtration under nitrogen, customer complaints about product variability dropped sharply. These measures now define our standard operating procedures.
In another instance, solar technology developers in Asia flagged issues around electrolyte stability in real-world temperature swings. We set up accelerated aging studies, tracked color, viscosity, and electrical conductivity, and found that minor residual acidity caused drift in sensitive cells. By tightening our post-synthesis neutralization and adding more robust packaging, we're now shipping bottles that maintain specifications for over twelve months, even in challenging storage environments.
Chemists working on bench-scale syntheses in academia or small industrial settings frequently face the frustration of scaling up only to see product behavior change unexpectedly. Our production engineers offer insight into viscosity management and agitation—lessons gained from batch-to-batch monitoring under different load and stirring speeds. In practice, longer alkyl chains require more vigorous mixing to blend efficiently, which can push overhead stirrers or pumps to their limits if not spec’d correctly.
Scaling packages from lab to pilot lines, we have navigated challenges like layering, sediment formation, and inconsistent yield. By investing in temperature-controlled reactors and online monitoring, we’ve created a production process that adapts responsively to small shifts. Conversations with procurement officers highlight another key lesson: packaging size flexibility, fast delivery, and reliable customs documentation streamline project planning for both in-house R&D and contract development teams.
University groups running screening arrays appreciate receiving product in smaller aliquots, each sealed under nitrogen. This approach cuts cross-contamination during rapid sequential trials and lets students run parallel experiments without introducing extra water or air via repeated bottle openings. After adopting this practice, academic collaborators have reported tighter error bars on their own measurements and fewer issues with inconsistent conversion or byproduct formation.
Industry users, particularly those in battery development or specialty separations, prefer larger volume drums with double-sealed liners. Handling protocols, worked out side-by-side with their facility managers, cut down transfer losses and managed electrostatic discharge risks. Some clients asked for rapid on-site technical support to bridge the knowledge gap in switching from traditional organic solvents to ionic liquids. Our technical team takes these opportunities to confirm best transfer methods, recommend compatible tubing and valve materials, and share firsthand knowledge about solvent compatibility.
While ionic liquids reduce many handling risks compared with volatile organics, we invest in regular hazard assessments and safety training. Personnel at our plants carry out hands-on drills for spill containment, and we distribute updated safety sheets directly to customer EHS teams. Our chemists have experienced firsthand how quickly an overlooked splash or improper labeling can lead to contamination or lost time. So we help end users adopt the same level of diligence, customizing training with insights gained through our own incident reviews and internal audits.
In the past, organizations have assumed ionic liquids are “green” by default. We encourage responsible use by providing peer-reviewed references, up-to-date environmental data, and support for lab-scale disposal protocols. Open communication ensures that environmental and occupational health teams are aware of the specific interactions and hazards tied to longer-chain halide ionic liquids.
Transitioning to new chemicals in a production or research setting often surfaces unforeseen hurdles. From imidazolium halide selection to post-processing adjustments, our team shares direct field experience to help others navigate the nuances. Regular feedback cycles, roundtable discussions with users, and open plant visits drive iterative improvements. Customers tackling complex synthesis, scaling up purification, or installing new process equipment can tap into this practical experience, reducing trial-and-error and saving valuable time.
By openly sharing failures and successes—whether it’s a viscosity spike in an unusually cold winter batch, a packaging tweak for export conditions, or a late-stage analytical hiccup—our relationships with downstream partners grow deeper. Together, we drive adoption of new ionic liquid tools that provide real-world value far beyond theoretical performance.
True maturation of a specialty chemical like 1-Dodecyl-3-Methylimidazolium Iodinide stems from constant feedback and a willingness to revise, upgrade, and invest in new testing. Our manufacturing journey reflects hundreds of conversations with researchers and production engineers, and every bottle ships packed with lessons learned. Instead of treating each order as a simple transaction, we treat it as the start of a new collaboration—one that brings together experience and ambition for the next round of innovation in chemistry and materials science.