Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing admin@sinochem-nanjing.com 3389378665@qq.com
Follow us:

N-Butyl-N-Methylpyrrolidinium Iodide

    • Product Name N-Butyl-N-Methylpyrrolidinium Iodide
    • Alias BMP-I
    • Einecs 606-219-5
    • 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

    933347

    Chemical Name N-Butyl-N-Methylpyrrolidinium Iodide
    Cas Number 52387-14-1
    Molecular Formula C9H20IN
    Molecular Weight 269.17 g/mol
    Appearance White to off-white crystalline powder
    Melting Point 128-132°C
    Solubility Water Soluble
    Density 1.41 g/cm³ (approximate)
    Storage Temperature Room temperature
    Purity Typically >98%
    Synonyms 1-Butyl-1-methylpyrrolidinium iodide
    Smiles CCCC[N+](C)(C1=CCCCC1)I
    Ec Number 611-469-0

    As an accredited N-Butyl-N-Methylpyrrolidinium Iodide factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 250 g of N-Butyl-N-Methylpyrrolidinium Iodide is supplied in a tightly sealed amber glass bottle with clear labeling and safety information.
    Shipping N-Butyl-N-Methylpyrrolidinium Iodide is shipped in tightly sealed containers, protected from moisture and light, and should be handled as a potentially hazardous chemical. It is packed according to relevant chemical safety and transport regulations, including labeling for irritants. Avoid rough handling, and store in a cool, dry, and well-ventilated environment during transit.
    Storage **N-Butyl-N-Methylpyrrolidinium Iodide** should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from moisture and direct sunlight. Keep it separate from strong oxidizing agents and acids. Store at room temperature, ideally between 15-25°C. Properly label the container, and use secondary containment to prevent accidental spills or leaks.
    Application of N-Butyl-N-Methylpyrrolidinium Iodide

    Applications of N-Butyl-N-Methylpyrrolidinium Iodide in Industrial Manufacturing

    As a direct manufacturer, we provide N-Butyl-N-Methylpyrrolidinium Iodide to a range of advanced chemical industries, supporting applications where high performance, purity, and traceability are critical for downstream formulation and process consistency. Below, we detail key application scenarios with a focus on sector-specific compliance, quantitative use, processing integration, and the types of end products realized by industrial consumers.

    1. Electrolyte Additive for Dye-Sensitized Solar Cells (DSSC)

    N-Butyl-N-Methylpyrrolidinium Iodide functions as an ionic liquid electrolyte component in the assembly of energy conversion devices, specifically DSSCs. Its selection addresses conductivity, ionic mobility, and stability benchmarks needed for scalable cell production, where batch-to-batch consistency and process qualification are controlled under photovoltaic industrial standards.

    Industry compliance standards

    • IEC 60904-1 Photovoltaic Devices — Measurement of Photovoltaic Current-Voltage Characteristics
    • RoHS Directive (2011/65/EU) for restrictiveness of hazardous substances
    • ISO 9001:2015 for Quality Management Systems in cell manufacture
    • IEC TS 62915 for performance testing and production qualification

    Typical usage ratio

    • 10–25% weight fraction in the total electrolyte formulation, adjusted based on target viscosity and ionic conductivity for the specific cell design

    Downstream process integration

    • Direct addition into the electrolyte mixture following solvent charging and complex formation with other iodide salts prior to cell injection under inert conditions

    Final product types

    • Dye-sensitized solar panels
    • Building-integrated photovoltaics
    • Portable energy harvesters for wearables

    2. Phase-Transfer Catalyst in Advanced Pharmaceutical Synthesis

    In pharmaceutical production, this quaternary ammonium iodide compound enables efficient coupling and alkylation reactions by enhancing ion transfer between immiscible phases during API synthesis. Manufacturers select and qualify this additive to meet regulatory requirements for residual solvent control and catalyst removal.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice Guide for Active Pharmaceutical Ingredients
    • USP General Chapter <791> for pH control in manufacturing
    • Ph. Eur. 2.3.2 Identification of Excipients in API production
    • 21 CFR Part 210-211 GMP for Finished Pharmaceuticals

    Typical usage ratio

    • 0.2–1.5 mol% relative to the main reactant; range adjusted following lab-to-plant scale optimization and efficiency screens for each reaction type

    Downstream process integration

    • Precise dosing into the reaction vessel post-charging of reactants, facilitating interphase ion transfer, followed by aqueous-organic separation before final purification steps

    Final product types

    • Pharmaceutical intermediates for third-generation cephalosporins
    • Active pharmaceutical ingredients for antiviral agents
    • Specialty alkaloids and heterocyclic APIs

    3. Electrochemical Device Electrolyte for Supercapacitor Production

    This ionic salt supports supercapacitor manufacturing as a non-flammable, electrochemically stable salt in high-voltage, room-temperature ionic liquid electrolytes. Its integration improves energy density, cycle life, and operating window, and manufacturers apply it in compliance with strict transportation and materials labelling norms due to its iodide content.

    Industry compliance standards

    • UN Manual of Tests and Criteria for Transport of Dangerous Goods
    • IEC 62576 for Electrochemical Capacitors — Performance Assessment
    • ISO/TS 16949 for Automotive-Related Supercapacitor Production
    • REACH Regulation (EC 1907/2006) for chemical registration

    Typical usage ratio

    • 15–30% by molality in ionic liquid matrix, proportion fine-tuned according to energy storage targets and electrolyte viscosity

    Downstream process integration

    • Careful dissolution into the base ionic liquid before electrolyte filling of supercapacitor cells under controlled-environment processing

    Final product types

    • Symmetric and asymmetric supercapacitor modules
    • Boost power packs for grid stabilization
    • Automotive start-stop systems

    4. Halide Source in Halide Exchange Reactions for Organic Synthesis

    Chemical and fine chemical industries use this compound as an iodide donor in halide exchange steps, including nucleophilic substitution and transhalogenation. Controlled iodide release and purity enable reliable downstream synthesis of iodinated aromatic and heterocyclic compounds for advanced organic intermediates.

    Industry compliance standards

    • ISO 14001 Environmental Management for chemical synthesis
    • Responsible Care Global Charter for material handling
    • ISO 9001:2015 for certified batch and analytical tracking
    • Globally Harmonized System (GHS) for substance labelling

    Typical usage ratio

    • Varies 0.05–1 eq relative to the substrate, optimized based on substrate reactivity and scale-up risk analysis for by-product minimization

    Downstream process integration

    • Dosed in the reaction mixture following careful control of moisture and competing nucleophiles; acts as a stoichiometric or catalytic iodide transfer agent depending on protocol

    Final product types

    • Iodinated aryl and alkyl compounds
    • Pharmaco-active halogenated intermediates
    • Specialty fine chemicals with specific halide patterns

    5. Ionic Additive in Organic Light-Emitting Diode (OLED) Materials Manufacturing

    Ionic additives such as this are incorporated during the formulation of active emitting layers for OLED devices. Compound use supports charge injection balance and emission layer morphology, with strict material qualification for performance uniformity and guarantees of impurity control during device stacking and encapsulation.

    Industry compliance standards

    • IEC 62341 for Organic Light Emitting Diodes (OLEDs) standards
    • JEITA EM-3701 for measurement methods and test items for OLEDs
    • ISO 9001 for traceable electronic grade raw material supply
    • RoHS Compliant in accordance with 2011/65/EU for finished consumer display products

    Typical usage ratio

    • 1–5% by weight in the OLED emitting layer, depending on desired charge mobility and resulting device emission profile control

    Downstream process integration

    • Added to organic solvents together with emitting and host molecules prior to thin-film deposition by spin coating or inkjet printing; batch controlled for layer reproducibility

    Final product types

    • OLED display panels for consumer electronics
    • Flexible and transparent lighting elements
    • Wearable OLED displays for medical and industrial monitoring
    Free Quote

    Competitive N-Butyl-N-Methylpyrrolidinium Iodide prices that fit your budget—flexible terms and customized quotes for every order.

    For samples, pricing, or more information, please call us at +8615371019725 or mail to admin@sinochem-nanjing.com.

    We will respond to you as soon as possible.

    Tel: +8615371019725

    Email: admin@sinochem-nanjing.com

    Get Free Quote of Sinochem Nanjing Corporation

    Flexible payment, competitive price, premium service - Inquire now!

    Certification & Compliance
    More Introduction

    N-Butyl-N-Methylpyrrolidinium Iodide: From Our Reactor to Your Innovation

    Crafting a Niche Ionic Liquid: Our Direct Experience

    Years of close work with heterocyclic chemistry and quaternary ammonium salt syntheses have shaped our understanding of N-Butyl-N-Methylpyrrolidinium Iodide. This product does not come from generic batch runs or bulk commodity lines—it comes from a focused, carefully controlled process where trace impurities and real-world reaction yields receive daily scrutiny. We listen to researchers, battery developers, and organic chemists who use ionic liquids in ways as diverse as catalysis research, electrolytes, and pharmaceutical intermediates.

    Chemists on our team first approached the challenge of producing N-Butyl-N-Methylpyrrolidinium Iodide not as a routine, but as an opportunity. Our reactors handle the N-alkylation of methylpyrrolidine under strictly monitored temperature, moisture, and halide environments to avoid mixed salts or residual byproducts. Moisture and trace organic amines can spoil the purity or hinder the performance in electrochemical devices, so we run every synthesis on actual demand.

    Getting the Chemistry Right: Physical and Chemical Profile

    With a molecular formula of C9H20IN, this compound typically leaves our drying line as a brilliant white to off-white crystalline powder. Analytical checks by gas chromatography and high-performance liquid chromatography remain routine, not just for regulatory points but because our customers care about current efficiency and signal noise. The iodide forms a wide electrochemical window, making it preferable for labs exploring next-generation batteries, room-temperature ionic liquids, or catalytic transformations.

    Water traces, halide balance, and particle size create subtle but real differences in how the compound behaves. Impurities at the ppm level may not show up in a COA, but during scale-up or when tested at sub-ambient temperatures, they expose themselves. In our operations, batches are split and checked using in-house NMR, in part to watch for overlapping methyl signals or unexpected splitting due to residuals, which is less common in more basic ammonium iodides, but vital here.

    Why Choose N-Butyl-N-Methylpyrrolidinium Iodide: User Perspective

    We often field questions from research teams wondering if this cation offers enough performance edge for batteries or synthesis. Compared to lithium salts or more widely-used tetraalkylammonium iodides, pyrrolidinium-based ionic liquids resist hydrolysis better, show greater chemical stability, and tolerate wider voltage swings without chemical breakdown. When developers move from smaller methyl or ethyl groups to butyl and methyl on the pyrrolidine ring, the phase behavior shifts, opening up design space for high-performance electrolytes or catalytic systems.

    No abstract branding or marketing here—just feedback from partners who see fewer contaminant peaks and more reproducible results in their NMRs or cyclic voltammetry runs. The difference comes down to how the larger butyl group balances fluidity and thermal stability while the methyl capping keeps viscosity from climbing too high, a sweet spot we have dialed in after repeated batches and bench feedback.

    Model, Specifications, and Improvements on the Bench

    The core product passes through multiple proprietary steps—some developed over decades—to reach the profile we now stand behind. Moisture content often measures below 0.05% by Karl Fischer, not just as a number but because too much water shortens shelf life and introduces redox problems in real-world experiments. Iodide content undergoes regular titration, ensuring stoichiometry. Purity benchmarks rest above 99.5% by HPLC, which is not a typographical boast but a necessary condition for the product to be accepted by advanced-energy labs testing against their own standards.

    Our team never assumes old process conditions fit new expectations. A decade ago, a 98% purity figure might have passed; today, labs spot impurities at 0.2% or lower. Clients synthesizing halide-exchange ionic liquids or building sensitive sensors demand slightly different particle sizes for optimal dissolution or coating uniformity, so we adjust our granulation and drying cycle time as needed.

    Each batch pulls from continuous improvement logs—data that comes from users working under inert glove boxes for battery research or pursuing atom-economical catalysis at room temperature. In the last two years, feedback on solubility in acetonitrile led us to tweak both the solvent removal process and the duration of the final vacuum drying cycle. There is no such thing as a “standard” run in this lab because users change, and so does our approach.

    Putting the Product to Work: Everyday Applications

    Researchers trying to build new all-solid-state batteries put a premium on ionic liquids that do not degrade at high voltages or leave behind halide residues, so this material appeals to them. In pharmaceutical R&D, teams use pyrrolidinium iodides as phase transfer catalysts due to their broad solubility profile. Organometallic chemists report fewer complications from non-specific side reactions when shifting away from ammonium salts toward products based on the pyrrolidinium framework.

    Teams working with this class of materials rarely stick to single-salt formulations. Co-solvent compatibility—especially with polar aprotic solvents—counts as much as the nominal purity number. We have watched university teams run full-cycle tests with our batches in sodium and magnesium batteries, then come back with requests for narrower particle size distributions or a different drying endpoint because their protocols evolved. Each field—be it electrochemistry, organic synthesis, or next-generation catalysis—demands not just analytical purity but the right combination of crystallinity, solvation energy, and resistance to oxidative decay.

    Comparing with Ammonium and Imidazolium Analogs

    Questions commonly focus on whether N-Butyl-N-Methylpyrrolidinium Iodide outperforms ammonium or imidazolium iodides. Chemical stability offers the most direct answer. Quaternized pyrrolidinium salts do not undergo the same alkyl cleavage or decomposition that ammonium analogs sometimes show over longer cycles or at higher voltages. Imidazoliums bring other advantages, such as lower viscosity and unique π-stacking in certain molecular assemblies, but tend to suffer from imidazole ring reactivity in oxidative environments. Pyrrolidiniums, in contrast, straddle a stable midpoint and occupy a useful niche in fields such as materials science, where thermal and chemical durability outweigh raw dielectric constants or simple melting points.

    From our own production notes, we see how the yield and isolation procedures change between these classes of salts. Imidazoliums often demand a longer purification and sometimes result in byproducts that fluoresce or interfere with UV-vis detection—a problem for sensors or photochemists. With pyrrolidinium-based salts, extraction, crystallization, and post-reaction filtration prove simpler, which reduces downtime and streamlines reprocessing if adjustments are needed between runs. We do not just compare numbers on paper; we watch what happens as real users push these classes to their limits.

    Continuous Feedback from Real-World Users

    Every year, we see more requests from new application areas—large-scale redox flow batteries, ionic liquid-gated transistors, and even some as-yet-unpublished medicinal chemistry projects building preclinical models. This diverse user feedback corrects our blind spots. Sometimes, battery teams ask us to run aging studies at 50°C; other times, catalysis researchers care about trace metal analysis to prevent transition-metal mediated side reactions. This is not oversight; it is collaboration. Only manufacturers living with the compound’s quirks day in and day out come to fully respect how complicated producing a “simple” salt can be.

    Our years in the plant taught us to expect the unexpected: drying a “finished” batch reveals new polymorphs, while a tweak to iodide grade resolves a previously intractable gelation issue during solvent exchange. Results come from batch records and operator logs, not press releases.

    Managing Purity, Scale, and Long-Term Storage

    One recurring reality: most downstream users need regular, closely-matched lots, produced without drastic process shifts in raw material sourcing or batch scheduling. We have invested in sealed, jacketed reactors to keep every gram away from airborne moisture and organic vapor cross-contamination. Once, a change in sealing wax for a reactor feed port led to a trace impurity at half a percent in a 100 kg batch. This taught us to check every input and maintain documented cleaning cycles for all gear.

    Packaging in amber glass or multilayer foil-lined drums reduces light- and air-induced decomposition. Real-world lab data shows that under dry nitrogen, N-Butyl-N-Methylpyrrolidinium Iodide remains stable for months, with no measured drop in purity by HPLC and no increase in conductivity value, which tracks ionic degradation. Store it open to humid air, on the other hand, and the material quickly absorbs moisture, clumps, and may lose its clean crystal edge—a fact backed not just by theory, but by losses recorded over years of warehousing.

    Listening to the Lab Bench, Not Just the Literature

    A product like N-Butyl-N-Methylpyrrolidinium Iodide never exists in a vacuum. The academic literature might highlight melting points, phase transitions, and X-ray crystallography profiles, yet misses out on batch-to-batch reproducibility and actual handling quirks. Over time, we discover how texture shifts with minor air exposure, or how fine-tuning the drying endpoint can add weeks to shelf life. Some of the best improvements in our plant have come from direct calls with users—folks who have run head-to-head tests against other iodide salts and came away with feedback more valuable than any published property table.

    Directly refining the synthetic pathway based not only on yields, but on ionic conductivity or UV-vis response, leaves us better equipped for practical challenges. This work matters for teams trying to optimize energy storage, design new gels, or build high-conductivity films for electronics. We do not overlook the day-to-day frustrations of researchers forced to re-prep or re-purify inconsistent lots—our own lab techs share the same challenges, and feed those daily observations back into every process iteration.

    The Importance of Documentation and Traceability

    As demand drums up for reliable sources of specialized salts, our clients ask more often for detailed batch records—including solvent logs, reaction temperature trajectories, and in-process analytical results. Producing N-Butyl-N-Methylpyrrolidinium Iodide here involves not just a reactor and a few chemicals, but a full suite of traceability tools. Each unit is tracked with full documentation of incoming raw iodide and pyrrolidine sources, as well as critical control points—our way of demonstrating that product from our plant meets expectations not by chance, but by design.

    Having invested in routine third-party spectral validation and in-house NMR, our QA department can catch “invisible” contaminants, including halide contamination or trace methylation byproducts, before they reach the customer’s bench. Frequent instrument calibration and direct material tracking deliver consistency not available from generic brokers or trading houses that purchase on the open market.

    Building for the Future: Sustainable Chemistry and User-Led Development

    In recent years, sustainability in manufacturing has shifted from a buzzword to a concrete requirement. N-Butyl-N-Methylpyrrolidinium Iodide production traditionally needed two-step alkylations, generating waste streams challenging to recycle. We’ve worked with chemical engineers to retool quaternization steps to enable minimum-waste protocols and solvent capture, dramatically reducing VOC emissions per batch. Customers in the battery sector often ask for greener profiles and certificates of origin. Our plant control panels display real time consumption rates for solvents, water, and energy, giving actionable data for efficiency upgrades.

    We have piloted ion-exchange and membrane purification methods for waste brine, achieving rebalanced halide recovery—translating to a documented drop in process waste over the last fourteen months. There’s no glory in discarding workable raw materials, especially as prices for pharmaceutical- and battery-grade iodide salts fluctuate with regulatory shifts and supply disruptions. Any future update on N-Butyl-N-Methylpyrrolidinium Iodide will depend not only on research trends, but also on finding new ways to trim process byproducts or adapt circular economy inputs.

    Real Partnerships Drive Practical Results

    We challenge ourselves to offer not a commodity but a partnership—a salt designed from molecular building blocks, produced for collaborators building tomorrow’s products. Every decision in synthesis, granulation, drying, and packaging echoes direct experience with customer labs. Demand for better ionic liquids in advanced batteries, supercapacitors, and synthetic methodology grows every year, especially for products customizable by reactivity, stability, and physical form.

    This connection to daily practice runs through every aspect of our work. We do not view manufacturing as just outputting lots from a formula sheet; we remember how a single missed impurity, an unseen color shift, or a marginal moisture increase causes downtime in a partner’s lab. As innovation cycles tighten and projects speed up, trust comes not from slogans, but from products that do exactly what researchers expect, again and again. If your group needs batch-specific modifications, further purification, or alternate packaging to match a new experiment, our line never hesitates to tune the next run.

    Looking Ahead: Meeting the Next Generation of User Demands

    From the earliest research labs experimenting with ionic liquids to today’s commercial battery developers and synthetic chemistry teams, the expectations placed on a specialty salt like N-Butyl-N-Methylpyrrolidinium Iodide continue to sharpen. We keep our ears open for new properties demanded by high-throughput screens, or the next round of regulatory standards set for pharmaceutical precursors and electronics-grade intermediates. Our own future depends on how quickly and precisely we translate these demands into improved chemistry, cleaner production, and strong technical support.

    Ultimately, this product stands as more than an entry in a catalog. For us, it represents not only chemical resilience and reliable supply, but a decades-deep habit of learning from the bench up. With every batch and every feedback loop, we grow along with the users and applications that build tomorrow’s technology. You can expect our material to evolve—one process improvement at a time—always anchored to both science and user reality.