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HS Code |
980721 |
| Chemical Name | 1-Octyl-3-Methylimidazolium Iodide |
| Cas Number | 35463-39-3 |
| Molecular Formula | C12H23IN2 |
| Molecular Weight | 322.23 g/mol |
| Appearance | White to off-white crystalline powder |
| Melting Point | 56-60°C |
| Solubility In Water | Soluble |
| Density | 1.3 g/cm³ (approximate) |
| Purity | Typically ≥98% |
| Storage Conditions | Store at room temperature, keep container tightly closed |
| Synonyms | [OMIM]I, 1-Methyl-3-octylimidazolium iodide |
| Incompatibilities | Strong oxidizing agents |
| Ec Number | None assigned |
As an accredited 1-Octyl-3-Methylimidazolium Iodide factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Supplied in a 25g amber glass bottle with a secure screw cap, clearly labeled with chemical name, CAS, and hazard warnings. |
| Shipping | 1-Octyl-3-Methylimidazolium Iodide is shipped in sealed, chemical-resistant containers to prevent moisture and contamination. It should be stored at room temperature, away from direct sunlight and incompatible substances. Packaging adheres to relevant hazardous material regulations, and all shipments include appropriate labeling and safety documentation to ensure safe handling during transit. |
| Storage | 1-Octyl-3-Methylimidazolium Iodide should be stored in a tightly sealed container, away from moisture and direct sunlight, in a cool, dry, and well-ventilated area. Keep it away from incompatible substances such as strong oxidizers and acids. Handle under inert atmosphere if possible, and minimize exposure to air to prevent degradation or hygroscopic absorption. |
Applications of 1-Octyl-3-Methylimidazolium Iodide in Industrial ManufacturingAs a dedicated manufacturer of high-purity 1-Octyl-3-Methylimidazolium Iodide, we supply this ionic liquid to a range of industries leveraging its unique solvating, conductive, and catalytic properties. Below, we outline real, established downstream applications, highlighting technical integration and compliance needs at each stage. 1. Dye-Sensitized Solar Cell (DSSC) ElectrolytePhotovoltaic manufacturers utilize this ionic liquid as a key constituent in electrolytes for dye-sensitized solar cells, benefiting from its stable ionic conductivity, thermal durability, and compatibility with redox couples. It supports efficient electron transfer and extends device operational lifespan by minimizing evaporation and degradation under illumination and thermal cycling. Industry compliance standards
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2. Electrochemical Sensor ManufacturingProducers of electrochemical sensors incorporate this ionic liquid as a conducting medium and electrode modifier, leveraging its high electrochemical stability and low volatility to facilitate reproducible sensor responses for oxidizable and reducible analytes, particularly in humidity- or temperature-sensitive conditions. Industry compliance standards
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3. Organic Synthesis CatalysisFine chemical and pharmaceutical manufacturers utilize the ionic liquid as a reaction medium and phase-transfer catalyst, facilitating halide exchange, nucleophilic substitution, and cross-coupling reactions. Its non-volatile nature and tunable polarity promote cleaner phase boundaries, faster rates, and simplified downstream product separation. Industry compliance standards
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4. Perovskite Solar Cell (PSC) Processing AdditiveAdvanced photovoltaic producers add this ionic liquid as a grain boundary and crystallization modifier for perovskite solar cell thin films, enhancing film morphology, moisture resistance, and device stability. Its iodide ions inhibit defect formation and support large-area, uniform film formation. Industry compliance standards
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5. Redox Flow Battery Electrolyte ComponentGrid-scale energy storage system integrators use this ionic liquid as a functional co-solvent or supporting electrolyte in redox flow batteries, where its broad electrochemical window supports high-voltage operation and mitigates crossover-related degradation in iodide- or bromide-based systems. Industry compliance standards
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6. Organic Dye Medium for Spectroscopic and Photonic DevicesManufacturers of spectroscopic instruments and laser dyes employ this ionic liquid as a low-volatility solvent for ionic or highly polar dye molecules, allowing fine-tuning of fluorescence quantum yield and extended operational stability in photonic devices subject to high-energy illumination. Industry compliance standards
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Behind every batch of 1-octyl-3-methylimidazolium iodide, there’s the practical experience learned from years of hands-on synthesis and real feedback from demanding research labs and manufacturers. In the lab, we see how this ionic liquid acts, how it responds to different reaction conditions, and where it gives the most value. Handling the synthesis and the downstream workup step-by-step, my team has seen how the product’s purity, stability, and consistent composition make it stand out from other ionic liquids. Processing this compound isn’t just about meeting purity targets on paper; it’s about ensuring the end product performs the same way every time in real-world applications.
The typical product we produce bears the chemical formula C12H23IN2, with a structure characteristic of imidazolium-based ionic liquids: a methyl group at the 3-position, an octyl chain at the 1-position, and iodide as the counterion. Every kilogram processed involves close monitoring, from controlling the water content down to parts per thousand, to minimizing halide impurities. Years of scaling up the synthesis—from pilot flasks to full-scale runs—have revealed where minor parameters can create issues. For example, water traces above a certain point compromise the ionic conductivity and can hamper device stability in applications like dye-sensitized solar cells. Removing these pockets of residual moisture takes patience, measured heat, and repeated vacuum cycles—no shortcuts if you want reproducible results.
Of course, our 1-octyl-3-methylimidazolium iodide doesn’t enter the warehouse until it passes checks for iodine and alkali metal content, not just a standard melting point check. Each lot runs through both HPLC and NMR control panels to confirm no backbone or side chain decomposition. Over time, customers have flagged rare side products, so we run extra screens for tetraalkylammonium adducts, which can form during prolonged or overheated alkylation. These controls matter particularly for applications that operate cells or assemblies sensitive to impurities, such as perovskite interfaces and certain organic syntheses.
Every year, new applications push the boundaries for what ionic liquids can do, but certain uses of 1-octyl-3-methylimidazolium iodide remain tried and true. Among all the compounds synthesized here, chemists tend to come back for this one because of its solvent properties, thermal stability, and ability to tune interfacial dynamics. In dye-sensitized solar cell research, our clients demand not just the ability to dissolve but to ensure the right ionic mobility for charge transport. An iodide counterion makes this product uniquely suited for redox mediation and acts as a reliable conductor of charge in specific electrochemical set-ups.
From years of customer feedback and lab observations, the octyl chain and methyl substitution impart less volatility and greater miscibility with a range of common organic solvents. In battery research, we’ve seen this ionic liquid offer lower viscosity than heavier alkyl chains but not so little as to compromise device stability. Here in the factory, we know the balance—there’s a reason we don’t ship an ethyl or dodecyl analogue more often for these tasks. For synthesis researchers, the iodide serves as a powerful nucleophile, enabling alkylation reactions and phase transfer processes that shorter or non-alkylated analogues can’t handle as consistently.
The pharmaceutical sector has experimented with the compound as both solvent and reactant. Process engineers report back how its melting range, ionic strength, and relative inertness help them devise easier separations or create less hazardous waste streams. We hear from bioanalytical labs that odd odors and color formation in samples often get traced back to unstable or easily oxidized halide solutions; here, our tighter controls on iodine and trace metal content have made a noticeable difference in long-term study reproducibility. Our own tests showed that perovskite thin films using our product exhibited improved homogeneity and lower defect rates.
Daily experience with ionic liquids reveals differences that aren’t obvious in catalog tables. In continuous manufacturing setups, we’ve compared dozens of imidazolium-based compounds, from small methyl and ethyl analogues to the more unwieldy dodecyl species. The octyl-methyl sandwich brings a practical midpoint. Compared to ethyl or butyl chains, octyl gives noticeably greater hydrophobicity and lowers water uptake for long-term uses, which protects sensitive anodes or cathodes in battery systems from degradation. Compared to longer alkyl chains, it keeps viscosity in check and cuts costs for stirring, pumping, and recovery.
Some labs try to substitute hexyl or butyl chains for cost reasons, but run into surfactant-like foaming or immiscibility with certain organic phases in production-scale operations. Short chain analogues often pick up more water or degrade under thermal load faster, hurting selectivity in chemical synthesis. On the other end, dodecyl analogues can precipitate or phase separate in complex mixtures, requiring more time or additional handling. In years of onsite trials, the octyl-methyl balance consistently hits the sweet spot for electrochemical and extraction workflows.
Iodide as a counterion offers further distinction. Chloride or tetrafluoroborate versions have different reactivity, often showing less chemical compatibility with nucleophilic substrates. In organic synthesis pipelines, iodide ions deploy better as leaving groups and redox partners, especially where strong nucleophilicity and soft base effects matter. Side-by-side pilot runs in the shop’s glass reactor banks proved the difference—in several classic alkylation reactions, the iodide version gave cleaner conversions and fewer byproducts compared to equivalents based on chloride or PF6.
For energy storage clients, iodide-based ionic liquids ensure iodine cycling in dye-sensitized solar cells or redox flow batteries. Synthetic substitutes using chloride or other halides fall short due to lower redox potentials or slower charge transfer. Several of our long-term partners in university and industrial research confirmed that octyl-methylimidazolium iodide supports greater long-term device stability, noticeably in higher open circuit voltage and lower degradation rates.
Working day after day with this ionic liquid, we see detail beyond what’s noted in typical spec sheets. Its relatively high thermal stability up to 200°C provides flexibility in processes—pressure reactors, gloveboxes, and benchtop syntheses all make use of this feature, reducing costly thermal management steps. The compound rarely emits strong odors, unlike some other halide-based ionic liquids, which helps maintain a better work environment. Clean handling reduces unnecessary exposure: here, we rely on glass, PTFE, or stainless steel, since iodide’s halide nature can corrode aluminum or softer metals over time.
The toxicity profile draws comparisons to other imidazolium ionic liquids. Long experience shows it handles without the volatility hazards of paeudo-solvent substitutes, and its chemical inertness keeps accidental exotherms rare when combined properly. Still, the compound doesn’t excuse careless handling—high concentrations or inadvertent heating above thermal decomposition can release iodine vapors. We store it in moisture-proof, light-resistant vessels and remind every team member to check seals and avoid repeated freeze-thaws, as this degrades product quality and, in extreme cases, causes container pressurization.
Disposal considerations also differ from standard organic solvents. While less environmentally hazardous than some halogenated options, we direct spent product streams to iodine recovery and halide neutralization systems built onsite. For research partners, we’ve provided practical waste stream recommendations after seeing how improper drainage caused pipe scaling or trace contamination in municipal water analysis.
Every quarter, demand for ionic liquids rises as new applications go mainstream, but shortages and inconsistent quality can cripple downstream innovations. Global disruptions in iodine supply chains have created swings in price and availability for iodide salts. From our side, forward planning with raw materials and regular product validation cuts surprises. Our sales partners note that when external suppliers run out or cut corners, lab productivity drops until a trusted batch gets delivered. Years of feedback from end users helped us quantify that customers notice yield dips or unexplained device failures far more with off-brand or inadequately purified material.
For solar cell manufacturers and research labs, the performance of a device often comes down to the reliability of its ionic liquid mediators. Device efficiency gains are undone by batch-to-batch inconsistency, short shelf life, or unplanned composition drift. This is where the manufacturer’s focus on trace impurities, moisture control, and repeatable synthesis plays a real role. We have heard from battery researchers who initially struggled with supplier-switching: unstable current, poor electrode compatibility, or sudden film delamination. Once they standardized on our factory-batched product, they reported fewer unexplained failures and more predictable performance metrics.
Scaling up for industry partners, we’ve tuned the purification process to either meet the low-metal-content targets for electronics or the high-concentration batches needed for bulk syntheses. In tens of thousands of kilograms delivered, returns traced to product issues remain rare—and, in those cases, feedback leads to further testing, batch quarantine, and improved internal training. Improvements aren’t just technical; they also affect safety and cost controls, as lesser byproduct formation allows easier separation and less reprocessing.
With greater industrial use, questions about toxicity and environmental fate become commonplace. Many ionic liquids, especially those carrying long-chain or halogenated ions, risk persistence or bioaccumulation issues if not handled responsibly. Based on our long-term waste analysis, 1-octyl-3-methylimidazolium iodide shows moderate persistence in lab conditions, with minimal off-gassing under normal operations. We route waste for iodine reclamation or safe chemical neutralization, not letting significant residues reach wastewater systems. The factory’s closed-loop system, combined with batch-level tracking, limits fugitive losses. Periodically, compliance officers audit our logs against environmental norms and verify that safe disposal protocols hold up in both episodic and routine discharges.
Occasional inquiries come in about regulatory status, particularly in the EU and United States. In each legislative zone, the definition of “environmentally friendly” changes from year to year, and the burden falls on us to document absence of banned contaminants and the trace level of heavy metals. We’ve invested extra resources in analytical verification, both in-house and using external validation labs, to stay ahead of new requirements.
In recent years, innovation has led to pushback against poorly characterized ionic liquids, especially where environmental persistence or toxicity become issues. Because we manufacture rather than simply trade, we keep detailed batch documentation extending from the raw material purchase through synthesis, purification, packaging, and shipping. Our customers ask to see certificates, spectra, and historic test data. In rare cases, trace odorants or off-coloration get flagged as potential indicators of oxidation or metal pickup. The plant’s iterative improvement program tracks these reports and acts to shut down recurring issues. For instance, repeated requests for higher “purity in air-sensitive devices” pushed us to upgrade vacuum filtration equipment and retrain staff on ultra-dry packing protocols.
Performance for 1-octyl-3-methylimidazolium iodide is tied directly to the depth of purification possible in a scaled operation. During pilot programs, lesser factories sometimes offer compounds at lower cost but without the controlled atmosphere or repeated recrystallization needed to meet high-end electronic specs. Experience on the factory floor makes one thing clear: minor tweaks in workup—a few hours longer on the rotary evaporator, a more tightly controlled nitrogen purge, better attention to cleaning glassware—add immediate value. We avoid “quick and dirty” shortcuts because they undermine application confidence and generate more returns and complaints.
During workshops with end users, we share practical tips on achieving maximum device performance. Suggestions include drybox storage even after shipment, minimizing air exposure during device assembly, and regular screening of small test quantities before committing to a full run. These lessons come from years of supporting both R&D labs and bulk production lines. In our own plant, we segment storage and packing areas for halide, BF4, and PF6 analogues, as cross-contamination tarnished several early projects and cost valuable time and resources to correct.
So far, comparative trials between our product and non-octyl analogues give the same outcome: higher retention of cell capacity in repeat cycling, longer shelf life of the packaged ionic liquid, and a noticeable drop in failed device rates. These aren’t abstract marketing claims—they come from roundtable discussions with returning customers, technical support logs, and periodic research partnerships.
It helps, too, to provide support well beyond a package’s delivery. For example, labs discovering unexpected residue or clouding in solution reach out to our technical team. Our specialists walk through storage conditions, re-filtering methods, and even application tweaks. Often, these issues stem from improper handling, partial solvent evaporation, or mismatched application temperatures. As a result, failure rates drop, and data reproducibility improves for the end user.
1-octyl-3-methylimidazolium iodide’s future broadens every year. Beyond solar and battery cells, new domains—ranging from advanced catalysis to next-generation separations—seek out this ionic liquid for its balance of hydrophobicity, stability, and conductivity. As researchers chase greener, more sustainable manufacturing, the product’s non-volatile nature and resistance to many common chemical hazards create opportunities for new closed-loop applications. Companies eager to green their processes experiment with ionic liquids as alternatives to traditional solvents, often reporting success in select syntheses or when minimizing hazardous waste.
Feedback circles between us and our industrial partners keep innovation alive. Every project that pushes the limits of purity, every novel application in microelectronics, or every complaint about performance is an opportunity to evolve manufacturing and support practices. As we invest in production and analytical upgrades, the compound’s reliability grows in parallel with its market footprint. Talks with large-scale manufacturers of photovoltaic materials and advanced synthetic intermediates point to rising interest in kilogram and ton-scale availability—something a committed manufacturer is best positioned to support.
Direct connections with users keep us grounded in reality. Large distributors rarely provide the technical troubleshooting or the willingness to adapt processing on the fly the way an engaged factory can. Over years, relationships build between manufacturing engineers, QC teams, and researchers in the field. The shared goal—consistent, high-performing ionic liquid for products that work as promised.
Every batch of 1-octyl-3-methylimidazolium iodide produced in-house benefits from firsthand experience. Watching synthesis in real time, responding to process hiccups, and tracking how raw material quality impacts fineness and yield teaches lessons no specification sheet captures. Factories that hand off these steps to third parties lose these critical insights, and issues with trace contaminants or variable performance grow over time.
Direct feedback loops between laboratory, manufacturing, and customers allow for faster problem resolution and smoother product evolution. QC protocols and analytical checks evolve as soon as patterns appear, without the delays of waiting for a distributor’s call or a reseller’s interpretation. The team quickly adapts to end user needs, whether it’s higher purity demands, custom packaging sizes, or targeted support for device troubleshooting.
By staying close to the production process, the chemical manufacturer—rather than a faceless supplier—builds deep knowledge that helps the customer unlock new performance improvements year after year. In real-world terms, that means fewer device failures, quicker troubleshooting, and more time spent pushing the technology, not diagnosing preventable material shortcomings.
With each batch dispatched, more factories, R&D labs, and device manufacturers trust in the consistency and reliability derived from direct manufacturing. As worksites grow more sophisticated and applications become more demanding, the lessons accumulated from continuous production, thorough QA, and honest customer feedback guide every improvement. That hands-on experience, grounded in day-to-day manufacturing reality, sets this product—and those who make it—apart from those forced to rely solely on secondhand reports or off-the-shelf stock.
In a world where new challenges and opportunities in fields from renewable energy to pharmaceuticals arise every year, that steady, practiced approach to ionic liquid manufacture becomes the cornerstone for progress. The story of 1-octyl-3-methylimidazolium iodide is written not just in catalogs, but in the details, learnings, and steady innovations from those who actually make it.