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HS Code |
138413 |
| Chemical Name | 1-Cyanopropyl-2,3-Dimethylimidazolium Chloride |
| Cas Number | 1235574-54-3 |
| Molecular Formula | C9H14ClN3 |
| Molecular Weight | 199.68 g/mol |
| Appearance | White to off-white solid |
| Purity | Typically ≥98% |
| Melting Point | 120-125°C |
| Solubility In Water | Soluble |
| Storage Temperature | Store at room temperature, dry place |
| Iupac Name | 1-(3-Cyanopropyl)-2,3-dimethyl-1H-imidazol-3-ium chloride |
As an accredited 1-Cyanopropyl-2,3-Dimethylimidazolium Chloride factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 1-Cyanopropyl-2,3-Dimethylimidazolium Chloride is supplied in a 100g amber glass bottle with a tamper-evident screw cap. |
| Shipping | 1-Cyanopropyl-2,3-Dimethylimidazolium Chloride is shipped in tightly sealed containers under ambient conditions. The packaging ensures protection from moisture and contamination. Proper labeling and documentation for hazardous materials are included, complying with local and international transport regulations. Handle with care to avoid spills or exposure during transit. |
| Storage | 1-Cyanopropyl-2,3-dimethylimidazolium chloride should be stored in a tightly closed container, in a cool, dry, and well-ventilated area, away from heat and incompatible materials such as strong oxidizers. Protect it from moisture and direct sunlight. Store at ambient temperature unless otherwise specified by the supplier. Properly label storage containers and follow all relevant safety and handling guidelines. |
Applications of 1-Cyanopropyl-2,3-Dimethylimidazolium Chloride in Industrial Manufacturing1-Cyanopropyl-2,3-Dimethylimidazolium Chloride serves as a functional ionic liquid in several high-value and technically demanding industrial sectors. With clearly defined downstream applications in select fields, this ingredient delivers process-specific performance in scenarios requiring compliance with strict industry standards. Below are key industrial uses based on established customer production practices. 1. Electrolyte Additive in Lithium Battery ManufacturingManufacturers of advanced lithium-ion batteries use this ionic liquid to improve electrochemical stability, cycle life, and safety of high-energy cells. It addresses requirements for thermal and chemical resistance within electrolyte systems, supporting development of next-generation power storage solutions for automotive and stationary markets. Industry compliance standards
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2. Phase-Transfer Catalyst in Pharmaceutical API Synthesis1-Cyanopropyl-2,3-Dimethylimidazolium Chloride functions as a phase-transfer catalyst in regulated pharmaceutical manufacturing, specifically for active pharmaceutical ingredient (API) syntheses where efficient, selective catalysis across immiscible phases improves yield and purity of high-value molecules. Industry compliance standards
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3. Antistatic Agent for Engineering Plastics ProcessingProcessors of specialty engineering plastics incorporate this ionic liquid to impart permanent antistatic performance for electronic device components, precision packaging, and technical films, addressing strict discharge requirements in electronic and cleanroom applications. Industry compliance standards
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4. Chromatography Medium for Analytical LaboratoriesAnalytical laboratory suppliers and contract research organizations employ this ionic liquid as a mobile phase modifier for high-performance liquid chromatography (HPLC), specifically to tailor retention, selectivity, and peak resolution in the separation of polar, basic, or ionogenic analytes. Industry compliance standards
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5. Supported Catalyst for Fine Chemical SynthesisProducers of specialty fine chemicals employ immobilized 1-Cyanopropyl-2,3-Dimethylimidazolium Chloride on solid carriers to enable recyclable catalysis in green chemistry processes, focusing on applications such as selective alkylation, transesterification, and condensation reactions under mild conditions. Industry compliance standards
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Every batch of 1-Cyanopropyl-2,3-Dimethylimidazolium Chloride leaving our factory reflects a history of trials and adjustments rooted in everyday production realities. Our team has spent years refining the synthesis and purification routines, and each modification—whether increasing reactor temperature ranges or switching out filter media—has been grounded in clear, measurable outcomes. We’re not in the habit of cutting corners, and every process change gets tracked all the way to a finished product. After all, material consistency and purity form the backbone of downstream results, so we treat them with seriousness.
Recent advances in ionic liquids have pushed us to take a hard look at both molecular design and scale-up. 1-Cyanopropyl-2,3-Dimethylimidazolium Chloride stands as our answer to repeated calls from applied researchers and process engineers for a more robust, task-specific alternative that avoids the usual pitfalls. Some ionic liquids break down under heat, others absorb water too quickly or show poor ionic conductivity. The product we’re discussing moves the dial forward, holding steady in temperature swings and resisting hydrolysis.
We manufacture this compound using a two-stage process. First, a meticulously designed quaternization step introduces the methyl groups at the imidazolium core, while nitrile-functionalization at the propyl chain brings in unique polar properties. The chloride counterion, from years of direct feedback, offers a more stable and predictable platform than some alternative anions. In our experience, the crystalline product forms efficiently without long residence times, minimizing batch waste and maximizing throughput.
Purity sits above 99%, as verified by controlled HPLC and NMR runs. We use Karl Fischer titration to keep water content tightly controlled, ensuring no excess moisture carries forward to customers. Granular attention to decomposition limits—recorded at temperatures above 220°C—means industrial users can push processing applications without worrying about premature product failure. We continually cross-validate with GC-MS to catch trace organic impurities before the product reaches packing lines.
Our early experimentation with the cyanopropyl functional group began in response to requests from pharmaceutical and process chemists seeking more selective extraction agents and solvents. The nitrile moiety interacts strongly with cationic and neutral species. At the bench scale, researchers observed improved solubilizing power for hydrophobic organics and increased selectivity in metal extraction—results later confirmed by our own application chemists using standardized metrics.
In battery applications, for instance, the combination of the polar nitrile and the imidazolium backbone results in a higher electrochemical stability window. This means fewer side reactions in high-voltage environments, and our lab has repeatedly measured minimal byproduct buildup after simulated cycling conditions. Colleagues in catalysis note that transition metal centers coordinate differently in the presence of the cyanopropyl chain, influencing both rate enhancement and selectivity: the effect is reproducible, not anecdotal.
Many users draw comparisons between our 1-Cyanopropyl-2,3-Dimethylimidazolium Chloride and the classic 1-butyl-3-methylimidazolium chloride. Experience shows that the cyanopropyl version exhibits far less volatility in hydrophilicity across variable temperature and humidity. The extra nitrile group, though subtle on paper, leads to meaningful shifts in extraction efficiency and ionic conductivity, particularly in low water activity systems. Our QA teams frequently benchmark the two materials against one another in-house, using the same feedstocks and methods to capture direct, actionable data.
Some older imidazolium salts struggle with discoloration or product breakdown after repeated thermal cycles. Consistent feedback tells us that the cyanopropyl structure resists side-chain cleavage, giving customers a longer shelf life and reducing the need for stabilizers or frequent replacement. Operators in synthesis labs often relay that their equipment needs less aggressive cleaning cycles, due to a reduction in byproducts permanently binding to glassware. None of these effects are accidental; they trace straight back to years of incremental design work and practical trial.
Our primary users span fine chemistry, electrochemistry, energy storage, and separation science. At the bench and pilot scale, the ability of 1-Cyanopropyl-2,3-Dimethylimidazolium Chloride to dissolve both polar and nonpolar substrates clears away common productivity bottlenecks. Trained chemists report faster phase transfer rates in two-phase reaction setups, saving on process time and reagent costs.
In lithium battery manufacturing, our material’s stable ionic conductivity enables thicker separator layers without penalizing performance. Operators find that their cell lines need less frequent adjustment, and waste rates drop due to more consistent results. On the extraction side, hydrometallurgical plants have adopted the chloride salt to replace more aggressive solvents, citing not only better recovery yields but also reduced corrosion across reactor surfaces. Environmental and safety managers repeatedly point to the low vapor pressure and minimal leaching chemistry as critical improvements compared with legacy solvents.
Our own application development staff partner regularly with customer research teams. At a specialty pharma facility, direct comparison between our product and other ionic liquids resulted in higher selectivity during intermediate purification of a complex, multi-step synthesis. The improvement wasn’t marginal: isolated yields increased, and energy demand per batch dropped, supporting a tight production schedule. These outcomes drive home the point: small tweaks in molecular structure can mean large returns in the lab or on the plant floor.
As the original manufacturer, we draw on both customer reports and our own line operation data to keep the synthesis optimized. We learned early that temperature control during the methylation stage pays for itself later, as it keeps the side product profile manageable and cuts down on multi-step purification. Wet chemistry teams log every batch adjustment and trace the impact into the next production cycle. Field failures—rare as they are—lead straight back to root-cause investigation, not one-off patchwork fixes.
Modifying the anion isn’t a mere afterthought. After years of working with alternative halides and non-coordinating anions, we concluded that chloride not only curbs cost and waste, but also supports stable solution behavior across diverse applications—from extraction to analytical chemistry. Customers with highly sensitive processes express appreciation for predictable pH and minimal background reactivity, allowing precise measurements without frequent recalibration or concern about drift.
Ionic liquids come with their own set of issues: raw material variability, scale-up foibles, and downstream processing challenges all make appearances during the lifecycle of a chemical. Water pick-up during storage is a classic problem, impacting everything from melting point behavior to phase-separation efficiency. Our logistics team works with packaging designers to ensure each shipment leaves in moisture-resistant containers, tested under real-world atmospheric swings. When a customer flagged unexpected viscosity changes in warmer climates, our technical folks reviewed both factory process logs and transit routes. Together, we confirmed that amping up the drying regime post-crystallization made the ultimate difference.
Another hurdle lies in sustainable sourcing. Chloride-based routes reduce reliance on rare metals or corrosive acids, lowering overall environmental impact and handling costs. Still, we stay alert to new findings in the green chemistry literature, running our own LCA (life cycle assessment) as new studies prompt revisions in best practices. Not every improvement makes a headline, but the incremental wins—less waste at each distillation stage, smarter solvent recovery strategies—add up over time.
Our years running synthesis lines taught us an enduring lesson: small chemical changes produce significant process and product advantages. With each structural modification, our crew evaluates not just theoretical properties but practical trade-offs. In 1-Cyanopropyl-2,3-Dimethylimidazolium Chloride, the unique nitrile-functionalized chain became our favorite after months of real-world piloting. At some points, it seemed like every output variable—solubility, ionic mobility, or stability—traded off with one another. Dogged rinse-and-repeat testing, supported by direct customer trials, ultimately pinpointed a sweet spot where the advantages outpaced any minor limitations.
We recognize new technologies are rarely static. Our R&D group works in lockstep with customers advancing electrochemical processes, green extractions, and innovative polymer systems. They provide feedback sessions with our technical team, not just marketing lit. Real data shape our next generation of ionic liquids. In return, customer operations benefit from shared knowledge: trends we spot in heavy industry sometimes provide solutions to university lab-scale problems and vice versa.
Expansion into cross-continental shipping brought added scrutiny to product hygiene and container resilience. Years back, a cargo delay led to moisture ingress on a single lot. Our in-house QA caught it early, but the experience shaped our next steps. We tightened inspection protocols and upgraded packaging inventory to triple-laminated materials. No roll-out occurs unless stability is confirmed across seasonal shifts and shipping distances. There’s no point in delivering a product that matches the spec on paper if it underperforms on arrival. Customers operating continuous-flow plants can’t afford excuses, and neither can we.
As scale increases, so does the frequency of process audits and internal sample checks. Routine cross-checking between production and lab teams ensures that analytical data stay consistent batch-to-batch. We deploy parallel samples for storage testing so that claims about shelf-life or performance longevity have a data trail to back them up. Customers often call for fresh lot tracking—particularly in high-purity or regulated sectors—so we keep well-annotated production logs and offer supporting analytics as needed.
A decade’s experience taught us that sometimes the largest challenges don’t stem only from chemistry but from shifting regulatory or end-user requirements. Jurisdictions change labeling rules, environmental compliance targets get raised, and chemical registries ask for new disclosure formats almost every year. Our compliance staff stay on point with industry bodies and legal updates, embedding regulatory monitoring right into R&D and finished product release. That way, shipping schedules stay predictable, and end-users spend less time on paperwork and more on core research or production priorities.
Based on requests from pharma, electronics, and environmental processing sectors, we track, record, and log the origins and handling histories of all incoming materials. Each step proves vital in the event of a safety check or audit, especially as customers lean into traceability. A clear trail, paired with real QC analytics, reassures partners that the ionic liquid reaching their facility is what we claim—and not a mixed or degraded surrogate.
Process engineers and bench chemists spot the real differentiators faster than any spec sheet can describe. With our cyanopropyl-functionalized chloride, they report less clogging in filters and glass columns, longer run times before column regeneration, and easier cleaning. In electrochemical setups, users experience fewer current drops and minimal panel fouling, especially under repeated cycles. All that means less downtime, more predictable maintenance, and higher usable yields.
These details—the kind passed on during shift changes or in lab notebook side notes—carry weight in procurement and plant management meetings. When a solvent reduces corrosion, that means not just improved numbers on a life cycle spreadsheet, but real safety benefits and reduced replacement costs for gaskets and seals. For us, hearing that teams can stretch operating intervals or switch seamlessly between product lines brings as much satisfaction as hitting routine production goals.
We don’t believe in putting a product on autopilot after a successful launch. The focus remains on building incremental gains—a few percent yield increase or a notable impurity drop may not grab headlines, but when multiplied over thousands of liters, the impact can rival the gains from major capital investment. Listening to customers helps us shape each round of updates, and as researchers press into new fields like solid-state batteries or closed-loop recycling, our development direction pivots alongside them.
Open communication keeps ideas and issues flowing. A researcher reporting unexpected results or bottlenecks can expect a callback and direct action, not a generic acknowledgment. Our staff keep regular contact with application scientists and process engineers, and these field inputs find their way back to reactor control charts or crystallization parameters. That spirit of two-way collaboration keeps our ionic liquids portfolio—and especially 1-Cyanopropyl-2,3-Dimethylimidazolium Chloride—in tune with the actual needs of modern industry.
From our vantage at the coalface of chemical manufacturing, we see 1-Cyanopropyl-2,3-Dimethylimidazolium Chloride as more than a compound or catalog entry. Its evolution stemmed from dozens of conversations, countless failed trials, and customer pain points aired without sugarcoating. Each bottle carries a record of those efforts and the real wins—greater process reliability, lower failure rates, and new possibilities in demanding applications. For users pushing research or production into new territory, the gains of this product are far from theoretical—they’re measured, documented, and grounded in daily factory performance.