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HS Code |
665840 |
| Chemical Name | 1-Octodecyl-3-Methylimidazolium Hexafluorophosphate |
| Molecular Formula | C26H51F6N2P |
| Molecular Weight | 540.66 g/mol |
| Appearance | White to off-white solid |
| Cas Number | 865404-08-4 |
| Melting Point | 47-49°C |
| Solubility In Water | Insoluble |
| Density | 1.13 g/cm3 |
| Purity | Typically >98% |
| Storage Temperature | Room temperature |
| Boiling Point | Decomposes before boiling |
| Ionic Liquid | Yes |
As an accredited 1-Octodecyl-3-Methylimidazolium Hexafluorophosphate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | A 100-gram amber glass bottle with a tightly sealed cap, labeled for 1-Octodecyl-3-Methylimidazolium Hexafluorophosphate, featuring hazard warnings. |
| Shipping | This chemical, 1-Octadecyl-3-methylimidazolium hexafluorophosphate, is shipped in tightly sealed containers, protected from moisture and light. It should be transported as a hazardous material in accordance with local, national, and international regulations, with appropriate labeling. Handling requires safety measures to prevent exposure and environmental contamination during shipping. |
| Storage | **1-Octodecyl-3-Methylimidazolium Hexafluorophosphate** should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area. Protect it from moisture and direct sunlight. Store away from incompatible substances such as strong oxidizers and acids. Use personal protective equipment when handling. Ensure the storage area is clearly labeled and complies with local chemical storage regulations. |
Applications of 1-Octodecyl-3-Methylimidazolium Hexafluorophosphate in Industrial ManufacturingAs a specialist manufacturer of 1-Octodecyl-3-Methylimidazolium Hexafluorophosphate, we work closely with process engineers and formulation chemists in multiple downstream sectors. The following application scenarios are based on actual industrial demand, regulatory context, and quality benchmarks in the chemical, materials, and advanced manufacturing fields. 1. Electrolyte Additive for High-Performance Lithium Battery CellsProducers of advanced lithium secondary batteries incorporate this ionic liquid as an electrolyte additive to enhance electrochemical stability and thermal safety. Its function supports stable cycling and reduces risk of dendrite growth in both NMC and LFP systems for energy storage, EV, and power tool batteries. Precise dosage adjustment depends on the desired conductivity and voltage window, along with the base electrolyte solvent and active materials. Industry compliance standards
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2. Antistatic Agent in Engineering Plastics CompoundingThe material serves manufacturers as a functional antistatic additive, especially for polyolefins, engineering resins, and composite plastics used in electronic housings, automotive interiors, and medical device components. Its ionic nature helps dissipate static charges and provides durable antistatic performance even after repeated cleaning and exposure to environmental humidity. Implementation must meet end-use migration and toxicity guidelines for materials in sensitive applications. Industry compliance standards
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3. Phase Transfer Catalyst in Fine Chemical SynthesisOrganic synthesis plants utilize this ionic liquid as a phase transfer catalyst to accelerate anionic and nucleophilic reactions between hydrophilic and lipophilic substrates. Real-world use cases include alkylation, esterification, and synthesis of functionalized heterocycles in pharmaceutical intermediate manufacture, aroma chemicals, and specialty agrochemical production. The imidazolium core provides solubility in organic phases and promotes efficient reactant transfer at the phase boundary, reducing reaction times and improving yields without introducing metal residues. Industry compliance standards
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4. Surface Modification Agent in Nanomaterial FunctionalizationProducers of nanomaterials and advanced pigments select this ionic liquid to functionalize particle surfaces for improved dispersibility and compatibility with organic or inorganic binders. It helps stabilize nanoparticles such as TiO2, SiO2, or carbon black during wet and dry milling steps, allowing for targeted surface energy adjustment. End users benefit from better particle distribution and long-term stability in high-value composite coatings, inks, and polymer nanocomposites, with attention paid to downstream migration and safe handling criteria. Industry compliance standards
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Working in chemical synthesis for decades, we see customers asking for more specialized ionic liquids every year. The lab world evolves quickly. Among the various compounds we’ve produced, 1-Octodecyl-3-Methylimidazolium Hexafluorophosphate stands out for its versatility in research. Long-chain imidazolium salts have generated great interest in the last ten years. Customers use this compound as a solvent, surfactant, and phase-transfer agent, especially for those searching for strong thermal stability combined with the specific hydrophobicity this class delivers.
Each batch of our 1-Octodecyl-3-Methylimidazolium Hexafluorophosphate goes through strict analytical checks. Purity matters in academic and industrial research; a trace impurity can throw off an entire synthetic route. By using advanced chromatography, NMR, and moisture analysis, we assure a compound fit for controlled, reproducible results. Our staff have designed a purification path that focuses not just on crude yield but on achieving minimal residual starting materials and side products. Customers won’t face stuck reactions due to hidden halides or short-chain imidazolium by-products.
Chemists are not looking for every imidazolium salt, but the C18 alkyl chain on the cation makes a significant difference in several applications. We have seen our clients rely on this product for colloidal stabilization, liquid crystal formation, and ionic liquid-based extractions. In catalysis, the long alkyl chain provides valuable amphiphilic properties. Extracting rare earths and precious metals becomes more efficient because of the unique hydrophobic pocket this compound produces around the metal. Surfactant formulation for nanomaterials—such as silver nanoparticles or gold nanorods—often falters with shorter chain imidazolium salts leading to unstable dispersions. The C18 tail in our model (catalog reference: OMI-PF6-C18) allows for a compact interface and reduces aggregation. Chemists working on materials science have pushed for the development of ionic liquids with a distinct separation between polar and nonpolar domains; this compound meets those needs.
From our lab, 1-Octodecyl-3-Methylimidazolium Hexafluorophosphate comes as a white to faintly off-white solid. Melting point hovers around 43-48°C, which means it can be handled at room temperature. It readily dissolves in a wide variety of organic solvents, including chlorinated and aromatic systems. Water solubility remains negligible, and this feature drives high selectivity in extractions. Each lot must pass moisture tests ensuring water content below 0.1%. We track and log conductivity and ion exchange performance; these properties allow our customers greater reliability when they scale up. No two labs work with the same priorities; we offer documentation for every parameter we measure, so project timelines are shortened without extra troubleshooting.
As ionic liquids grow into mainstream chemical processes, we see their use expand beyond niche academic questions. Early on, some viewed long alkyl chain imidazoliums as impractically hydrophobic or difficult to handle compared to the C2 or C4 imidazolium salts. Our experience has shown the opposite in applications where you need strong surface activity or immobilization. In liquid–liquid extraction, researchers report sharper phase separations and stronger retention for transition metals. Colleagues in the energy storage field asked us for ionic liquids with longer tails. Here, the compound’s non-volatility and electrochemical window pay off during the development of safer electrolytes for supercapacitors. The aftertaste of halide contamination plagued our clients working with functional materials – steps in our process target and purge such pitfalls, allowing for true long-term stability in ionic liquid applications.
Our product enters a crowded space of imidazolium-based ionic liquids, many featuring methyl, ethyl, or butyl side chains. Yet, the octodecyl tail dramatically alters physical behavior. In common C2-methyl (EMIM) or C4-butyl (BMIM) versions, higher room-temperature fluidity means they evaporate faster and show higher miscibility with water. This becomes a flaw in two-phase systems demanding water-immiscibility. Our long-chain version resists water uptake, and precipitation rarely occurs under typical use conditions. Some short-chain imidazolium products promote undesirable foaming or auto-aggregation that complicates workup. With OMI-PF6-C18, customers report cleaner separations, less foaming, and sharper interphase boundaries. In addition, we see marked improvements in product stability during storage. Shorter chain compounds degrade more easily under UV, while the octodecyl version holds up during daylight exposure and repeated heating cycles.
Our team has dissected batch failures caused by commercial suppliers in the past. Moisture, residual imidazole, and unreacted alkyl halide bring headaches. During scale-up, those impurities reduce yield and introduce process variability. That’s why we have introduced a double ion-exchange purification plus vacuum drying. Each batch spends over 24 hours under high vacuum with continuous temperature cycling. Experience with scale-up means we anticipate purification sticking points: we avoid bulk crystallization from high-polarity solvents in favor of controlled precipitation, minimizing occluded electrolyte impurities. The result shows up in less frequent reprocessing and more usable material straight from the bottle.
You can find ionic liquid recipes online, but translating bench chemistry to industrial supply requires more than copying literature protocols. Raw material selection plays a key part—our teams select electrophiles in lots with GC-traceable purity and minimize chemical exposure to ambient air. Standard glassware sometimes leaches sodium and boron, which then appear as unpredictable spectroscopic noise. We run glassware cleaning and drying cycles far beyond typical academic preparation, so each vessel only contributes the intended chemistry. Constant analysis of side reactions and batch-to-batch comparison forms our feedback loop. Input from customer projects also shapes our manufacturing – for example, after field feedback that initial lots of OMI-PF6-C18 discolored during silver nanoparticle formation, we retooled the ion-exchange sequence and expanded spectral monitoring.
Lab directors tell us that timelines continue to shrink. Material delays, failed lots, or sample impurities set back multi-million dollar programs. By tailoring our logistics and communication to suit research timelines, we help labs stay on schedule. Field engineers document shipping metrics and storage advice based on frequent feedback. We switched to amber glass containers to reduce photodegradation; we monitor shelf stability biweekly under typical storage conditions. Customers appreciate frank documentation about solubility quirks and temperature handling – OMI-PF6-C18 sometimes forms a viscous slurry at low temperatures, which can be reversed by gentle warming. Gel formation in cold weather is not a failure, but part of the expected physical behavior for C18-tailed imidazolium salts. We encourage all new users to consult our chemists before scaling up, leading to routine savings on time and cost.
Chemistry grows bigger, but the responsibility for environmental performance grows too. Ionic liquids do not simply trade one hazard for another. During plant operation, we recover and recycle spent cleaning solvents rather than sending them to waste. Hexafluorophosphate counterions sometimes concern customers, given the global move away from persistent fluorinated compounds. We continually monitor regulatory proposals and test alternative anions under real-world conditions. Customers who need technical support on disposal or reclamation find our product labeling matches the latest requirements. In teaching customers to handle and dispose of OMI-PF6-C18, we focus on practicality—transport in original containers, protect from high humidity, and avoid mixing with incompatible acids or bases.
Even among knowledgeable chemists, some misconceptions about ionic liquids persist. Several clients ask about solvent reactivity—some believe all imidazolium salts show inertness toward metal halides, which is not always true. We provide reactivity data based on storage with common test metals, showing which systems are compatible for long-term storage. A number of others wonder if ionic liquids uniformly boost reaction yields. Experience shows no universal rule. The right solvent improves selectivity and reduces side-product formation—this holds for hydrophobic systems only in specific examples. The C18 chain in our OMI-PF6-C18 widens application, but doesn’t replace empirical screening. For those new to ionic liquids, we offer trial packs and demonstrations, sharing not just results but pitfalls—mistaken solvent selection wastes both time and money.
Industries move fast, and our product development matches that pace. In electronic materials, customers prize ionic liquids that maintain dielectric constant stability across a range of voltages and temperatures. The C18 tail offers fewer extraction artifacts in analytical labs, reducing background interference. Environmental labs use OMI-PF6-C18 in the preconcentration, extraction, and stabilization of trace analytes. Performance in pilot-scale projects drives adoption – high-boiling solvents such as this one cut lost mass during distillation or granulation. Our reliability attracts not just researchers but production chemists searching for less downtime and more predictable outcomes.
Attention often runs to the shortest chain imidazolium salts, which are easier to synthesize but miss out on phase behavior required for modern extractions. BMIM-based (butyl) options see wide use for general catalysis but falter in two-phase systems, bringing unwanted hydrophilicity. EMIM (ethyl) versions can polymerize under strong UV exposure and cause unpleasant odor issues after short storage. Many labs first resist the higher cost of long-chain products; once projects fail from cross-phase contamination or byproduct haze, they return to OMI-PF6-C18 for improved yields. Few products match its balance in selective organic phase extraction, and even fewer combine that with strong thermal and oxidative durability. Our documentation draws on dozens of customer examples to clarify exactly which system demands a C18 tail versus a C4 or C8 version.
Our work extends well beyond shipping containers of ionic liquid. We see every new customer application as a feedback opportunity. By documenting use cases and project histories, we help new projects avoid common pitfalls—whether through direct supply of customizations, or simple advice on batch scale and handling. Sometimes, what matters are not purity or physical parameters alone, but the willingness to trace a problem until it leads to a solved process. Our team takes each complaint or question to heart, using it to refine process step or packaging. We’ve adapted shipping protocols when customers encountered issues importing ionic liquids across climate zones, and swapped suppliers when raw material batches didn’t meet specifications. This iterative approach – checking, adjusting, consulting – means that customers encounter fewer surprises. Reliability in account management and technical follow-up is just as critical as chemical purity.
Although the advantages of long-chain imidazoliums like OMI-PF6-C18 seem apparent, we do not claim universal fit. Higher viscosity at room temperature can complicate volumetric transfer in automated settings; at the same time, extreme hydrophobicity limits solubility for certain highly polar compounds. Laboratories planning to use ionic liquids in continuous-flow processes often need to re-examine agitation and mixing protocols for high viscosity phases. We address these issues in technical bulletins, offering empirically-tested dilution protocols or blending with co-solvents to assist phase transfer. The manufacturing world doesn’t stand still – we’re routinely testing next-generation imidazolium salts with different counterions, and developing tools to better monitor long-term shelf stability and reactivity for specialty applications.
We hear time and again from customers bringing our ionic liquid into real scale reactions. Projects stuck at the gram scale for months transition to multi-kilogram scale with much less troubleshooting. Many attribute this improvement to consistent product quality, but also to the open availability of supporting technical data. Some report increased reproducibility in catalyst recycling or nanoparticle stabilization. Our chemistry team maintains a project archive to track which process tweaks lead to greatest field benefit. These lessons feed a cycle of continuous improvement, adding direct, practical value for future customers.
No product earns user trust from a one-paragraph description. Years of customer feedback, problem-solving, and process development hone how we make 1-Octodecyl-3-Methylimidazolium Hexafluorophosphate. What sets the product apart isn’t just purity benchmarks. Our organizational memory, open technical support, and continuous adaptation define the actual value. In our view, providing feedback, sharing case studies, and rapidly addressing challenges builds the environment for successful research. Customers who partner with us get a product that reflects long-haul development—one rooted in laboratory realities and shaped by constant reexamination of techniques, outcomes, and scientific needs.