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1-Pentyl-2,3-Dimethylimidazolium Bromide

    • Product Name 1-Pentyl-2,3-Dimethylimidazolium Bromide
    • Alias [PMIM][Br]
    • Einecs 700-850-2
    • 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
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    Specifications

    HS Code

    798325

    Chemical Name 1-Pentyl-2,3-Dimethylimidazolium Bromide
    Molecular Formula C10H19BrN2
    Molecular Weight 247.18 g/mol
    Cas Number 197647-56-8
    Appearance White to off-white powder
    Melting Point Approximately 65-70°C
    Solubility In Water Soluble
    Purity Typically ≥98%
    Density Unavailable/Specialty compound (refer to supplier for precise value)
    Boiling Point Decomposes before boiling
    Storage Conditions Store in a cool, dry place, tightly closed
    Hazard Statements May cause eye, skin, and respiratory irritation
    Synonyms C5mimBr, 1-Pentyl-2,3-dimethylimidazolium bromide
    Iupac Name 1-pentyl-2,3-dimethyl-1H-imidazol-3-ium bromide

    As an accredited 1-Pentyl-2,3-Dimethylimidazolium Bromide factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 100 grams of 1-Pentyl-2,3-Dimethylimidazolium Bromide is packaged in a sealed amber glass bottle with a tamper-evident cap.
    Shipping **Shipping Description:** 1-Pentyl-2,3-Dimethylimidazolium Bromide is shipped in tightly sealed, chemical-resistant containers to prevent moisture absorption and contamination. Packages are clearly labeled, accompanied by Safety Data Sheets, and comply with relevant hazardous material regulations. Transport is under ambient conditions, avoiding excessive heat or direct sunlight, ensuring product safety and integrity during transit.
    Storage **1-Pentyl-2,3-dimethylimidazolium bromide** should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from moisture and direct sunlight. Keep the container away from incompatible substances such as strong oxidizing agents. Store at room temperature, and avoid extreme temperatures. Always ensure proper labeling and follow relevant safety guidelines for handling ionic liquids.
    Application of 1-Pentyl-2,3-Dimethylimidazolium Bromide

    Applications of 1-Pentyl-2,3-Dimethylimidazolium Bromide in Industrial Manufacturing

    As a direct manufacturer, we supply 1-Pentyl-2,3-Dimethylimidazolium Bromide for targeted use in advanced chemical processes. Our expertise covers integration into ionic liquid research, electrolytes for energy storage, catalysis for organic synthesis, and separation technology for challenging extractions. Below, we define primary application segments, focusing on concrete downstream processing requirements, validated compliance norms, workable dosage windows, and relevant product outputs.

    1. Electrolyte Formulation for High-Energy Supercapacitors

    Supercapacitor producers select our material to formulate high-stability ionic liquid electrolytes that support enhanced charge-discharge cycles and broaden thermal operating ranges. The cation structure enables low volatility and chemical stability under high voltage, allowing next-generation energy storage systems to function dependably in electric vehicle and grid applications.

    Industry compliance standards

    • IEC 62391-1:2020 (Fixed electric double-layer capacitors for use in electronic equipment)
    • RoHS Directive (2011/65/EU)
    • REACH Regulation (EC) No 1907/2006
    • Internal AEC-Q200 automotive electronic component validation (manufacturer-specific)

    Typical usage ratio

    • Commonly 12–40 vol% in organic or hybrid electrolytic systems; the dosage depends on interactions with target solvent system and required ionic conductivity for the cell. Pilot QC guides exact blending ratio adjustment based on ESR and capacitance targets.

    Downstream process integration

    • Added during liquid-phase electrolyte blending after solvent drying, followed by vacuum degassing, before electrode stacking and solvent injection in automated supercapacitor assembly lines.

    Final product types

    • High energy density supercapacitors for EV battery modules
    • Backup storage modules for industrial UPS systems
    • Consumer electronics backup capacitors
    • Grid balancing fast-discharge devices

    2. Homogeneous Catalysis in Pharmaceutical Intermediates Manufacturing

    Process chemists utilize the product as a reaction medium and cocatalyst for selective alkylation, acylation, and heterocycle formation steps in API precursor manufacturing. The ionic liquid phase can enhance selectivity and conversion efficiency under mild temperatures, improving downstream purification and reducing environmental solvent handling concerns.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • EU GMP Part II – Basic Requirements for Active Substances
    • 21 CFR Part 211 (US FDA cGMP for Finished Pharmaceuticals, relevant to process intermediates)
    • Ph. Eur. General Chapter 2.2.46 (Conductivity in pharmaceuticals production controls)

    Typical usage ratio

    • Used at 5–20 mol% relative to organic substrate; actual concentration adjusted for kinetic efficiency and isolation ease, as determined by process development labs for each synthetic transformation.

    Downstream process integration

    • Charged into multi-neck reactors alongside raw reactants after initial charge-in and temperature stabilization; removed via phase separation or vacuum distillation post-reaction step, before aqueous washes or further downstream transformations.

    Final product types

    • Chiral drug intermediates such as 1,3-dicarbonyl derivatives
    • Pyridine-based pharmaceutical intermediates
    • Fine chemical ligands for active API transformations
    • Complex heterocyclic building blocks for contract manufacturing pipelines

    3. Ion-Exchange Medium for Metal Recovery in Electronics Recycling

    Specialized recyclers employ this imidazolium-based compound as a non-aqueous ion-exchange medium to selectively bind and separate transition metals from shredded PCBs, used lithium-ion batteries, and photographic residues. The precise cation–anion interactions help achieve high metal selectivity and efficient back-extraction.

    Industry compliance standards

    • ISO 14001:2015 (Environmental Management Systems in metal refining)
    • OECD Test Guidelines for chemical hazard characterization
    • WEEE Directive 2012/19/EU (Waste Electrical and Electronic Equipment)
    • REACH compliance for chemical handling and effluent discharge

    Typical usage ratio

    • Implemented at 1–10% w/w versus total leachate depending on target metal ion load and batch extraction efficiency; ongoing monitoring guides dosing for each feedstock lot.

    Downstream process integration

    • Dosed into leachate-collection tanks after acid digestion of electronic scrap; ion exchange equilibrates under agitation before metal recovery via organic back-extraction in cascade separators and subsequent distillation to regenerate medium.

    Final product types

    • Recycled palladium, gold, and copper metal powders
    • Recovered lithium and cobalt salts for battery manufacturing
    • High-purity electronic metal oxides for circuit board refabrication
    • Electronic-grade recycled silver complexes

    4. Solvent for Cellulose Dissolution in Specialty Fiber Spinning

    Producers of high-performance regenerated cellulose fibers turn to this ionic liquid to dissolve highly crystalline cellulose, facilitating the controlled wet spinning of specialty fibers for filtration, medical, and performance textile sectors. The non-volatile, stable medium supports continuous fiber production with tailored cross-sectional density and minimal solvent loss.

    Industry compliance standards

    • ISO 9001:2015 (Quality management applied in fiber manufacturing plants)
    • OEKO-TEX Standard 100 (for downstream textile application safety; applicant needs supply chain traceability)
    • REACH Annex XVII compliance for worker exposure and environmental safety
    • Clean Production Action GreenScreen® (reference for chemical hazard analysis in textile input streams)

    Typical usage ratio

    • Cellulose content typically loaded at 7–15 wt% in the ionic liquid, with the total solvent volume determined by downstream fiber diameter specification and viscosity parameters tracked at in-process QC labs.

    Downstream process integration

    • The ionic liquid is charged into shear mixers before direct addition of cellulose pulp; post-dissolution, the viscous spinning dope passes through multi-orifice spinnerets, with excess solvent recovered from coagulation baths by closed-loop filtration and reprocessing units.

    Final product types

    • Ultra-fine filtration fibers for pharmaceutical and food-grade filters
    • High-tensile medical dressing filaments
    • Performance textiles for demanding industrial end-uses
    • Eco-friendly fiber blends for biodegradable nonwovens
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    Certification & Compliance
    More Introduction

    1-Pentyl-2,3-Dimethylimidazolium Bromide: Bringing Precision to Ionic Liquid Applications

    The Experience Behind Purpose-Built Imidazolium Salts

    Developing custom imidazolium salts has taught our team plenty about tailoring chemical structures to meet new research and industrial demands. 1-Pentyl-2,3-Dimethylimidazolium Bromide stands as a clear example of what focused molecular modification offers: a product that handles the core needs of advanced extraction, catalysis, and analytical chemistry, while giving users reliability and straightforward functionality.

    Customers ask about the role small alkyl chain variation plays in ionic liquids. Here, swapping methyl groups for bulkier alkyl chains—like the pentyl moiety—changes the overall viscosity, increases hydrophobic character, and fine-tunes the phase behavior. Through years of direct manufacturing feedback and active participation at industry meetings, we’ve watched how these property shifts reduce volatility in batch-to-batch processes, allowing researchers and engineers to cut troubleshooting time.

    Meeting Real Lab and Process Expectations

    Synthesizing 1-Pentyl-2,3-Dimethylimidazolium Bromide in-house brings several advantages. We control reagent purity, temperature profiles, and purification steps tightly, so chemists can avoid dealing with cloudiness, caked product, or unpredictable melting points. Each batch stays free of halide byproducts and inconsistent moisture loads: a small change, but one that matters for reversible phase studies and sensitive syntheses.

    Customers working in chemical separations report that this imidazolium salt brings better dissolution of both polar and non-polar substances compared to simple methyl or ethyl imidazolium compounds. Studies posted in peer-reviewed journals back those observations: the pentyl substituent broadens the range of target compounds for solubilization, especially in non-conventional liquid-liquid extractions or customized partitioning setups.

    Usage: Proof Lies in Adaptability

    Labs preparing reactive intermediates need chemicals that behave consistently, not just meet a list of formal specs. The long alkyl chain on the pentyl group pushes the cation’s lipophilicity, leading to stronger partitioning in organic-rich media. In pharmaceutical routes and natural product isolations, this property frees up paths that standard methylated imidazolium salts keep blocked.

    On our manufacturing benches, quality means every bottle delivers the same melting range, crystal structure visible under microscopy, and physical behavior you observed last quarter. That consistency flows right into your glove-box work, glass reactor runs, and pilot lines—minimizing time spent addressing the chemical quirks that follow third-party resins or inconsistently sourced precursors.

    1-Pentyl-2,3-Dimethylimidazolium Bromide works well in research where deep eutectic solvents or ionic catalysis are under the spotlight. With the pentyl tail, you see different self-assembly in solvents, changing how proteins, membranes, or ionic aggregates line up and respond to charge. Biochemists taking measurements with chromatography or spectrometry can depend on known interactions, improving reproducibility compared to earlier-generation imidazolium salts.

    Specifications We Hold Ourselves To

    In house, our technicians keep analytical instrumentation humming day and night. We insist on full NMR and FTIR verification for every production lot, matching carbon, hydrogen, and nitrogen ratios to published spectra and our own internal standards. Titration for bromide content gets checked by two analysts so nothing slips through that can foul delicate equipment or bias results. Part of any laboratory’s trust in a raw material lies in traceability; batch paperwork, instrument logs, and lot numbers stay accessible all the way back to raw feedstocks.

    Physical appearance continues to matter. Customers use our product both as solid crystals and as concentrated stock solutions; we filter out any undissolved remains so every container can serve straight from the bottle without fuss. QC flags any errant colorations or physical impurities early. Moisture levels remain critically low, since even half a percentage point of water by mass can change extraction equilibria or salt out another ingredient during synthesis.

    Differences That Change Laboratory and Industrial Practice

    The simplest change in a molecule’s chain length sets off a cascade of new outcomes for benchwork. The extended pentyl group adds a clear hydrophobic effect not available in commonly sold methyl or ethyl analogs. This matters in cases where researchers want to experiment with nonaqueous polar solvents or create biphasic systems with unusual interface tensions. As a manufacturer, seeing the experimental data match the theory—better mixing, more persistent phases—proves that these molecular tweaks matter.

    In the field, thermal stability and solubility set apart 1-Pentyl-2,3-Dimethylimidazolium Bromide from other quaternized imidazoliums. The longer chain brings a slight drop in melting point, so users working near ambient temperatures aren’t wrestling with premature solidification. This property also broadens its range in catalysis and phase-transfer work, especially when researchers need to run reactions at moderate heat without adding co-solvents.

    Technicians focusing on environmental or fuel cell applications benefit from improved ionic conductivity and less susceptibility to accidental water pickup. Our process steps cut down residual water content, as routine checks at different points of the dry-down verify that stray moisture levels don’t slip past the finish line. Every researcher wants clean, reliable results, so we’ve invested heavily in on-site Karl Fischer titration capability and real-time monitoring of room conditions during production and packing.

    Feedback From Users Across Industry and Academia

    The changes we make as a manufacturer don’t come just from journal articles. Most upgrades stem from hearing how product performance impacts protocols in downstream labs. Process chemists contacted us about scale-up for continuous flow systems, noting that previous imidazolium salts suffered from residue accumulation in small-diameter tubing. Since we built in additional filtration and phase-separation steps, the pentyl-2,3-dimethylimidazolium compound delivered clearer flows and fewer shutdowns for cleaning.

    Researchers in material science pass on stories about pushing deep eutectic solvent-salt systems toward new electrochemical uses. Their work demands clean sample prep and repeatable behavior across multi-week tests. A minor contaminant or unpredictable water gain turns days of measurement into write-offs—why our internal controls on trace metals and solvent residues often draw positive mention in published articles.

    We’ve seen organic chemists, environmental engineers, and even agricultural chemistry labs find value in this compound. Certain pesticide extraction protocols worked out in the mid-Atlantic US, as described in regional university case studies, ran with higher yield when medium-alkyl imidazolium salts replaced traditional shorter-chain cousins. 1-Pentyl-2,3-Dimethylimidazolium Bromide let teams clone protocols across laboratories without new solvent mixes or pH adjustments, speeding up the shared validation process.

    Looking Beyond the Usual List of Applications

    Chemistry doesn’t stand still just because a chemical gets a new label or a slicker brochure. Our experience watching application spaces grow—from academic pilot studies to real industrial practice—keeps us invested in sharing what works and discarding what doesn’t. Whereas early imidazolium-based ionic liquids stuck close to shared formulas and mainline use, the last decade’s need for custom solutions has carved out a space for careful chain choice, anion tuning, and stepped-in purification.

    Biotechnology teams who need solvents that don’t denature sensitive proteins or enzymes often complain about fine-tuning solubility and ionic strength. The five-carbon pentyl tail in this imidazolium salt stretches the set of proteins and biocompatible forms solvated, giving new ground for high-yield purifications or stabilization of transient complexes. In our facility, this means providing reproducible sample lots for beta testers—QC steps, not hunches, drive the product we ship out.

    Our direct connections to labs and process facilities mean we hear where generic manufacturers and third-party suppliers leave pain points. Some compounds behave well at kilogram scale but turn unreliable at grams; others hit quality plateaus where longer shelf life or thermal behavior wander. Steering clear of speculative claims, we document storage and handling conditions that result in two years of shelf stability, verified by re-analysis of retained samples and customer-resubmitted aged material.

    Challenges in Manufacture and Consistent Supply

    Manufacturing 1-Pentyl-2,3-Dimethylimidazolium Bromide presents no shortage of engineering hurdles. The pentyl chain introduces more volatility in the precursor, complicating distillation and phase isolation. Our chemists fine-tune reactor temperatures and vacuum pressure every run. Instead of relying on general-purpose glassware, we select vessels and seals that keep contamination minimal and provide tighter control over unwanted side reactions.

    Transitions in batch scale have taught us careful lessons on transfer losses and microevent water gain, especially during phase wash and salt isolation. Every storage vessel gets pre-dried, and routine environmental swabs help spot rogue halide traces or dust before they can impact final purity.

    Forecasting inventory has forced continual adaptation. Custom compounds like this attract project-based orders and urgent requests from process teams or research consortia. We learned to keep buffer stock, log regular stability tests, and adapt packing formats after seeing demand spike in new market areas. Small-lot customers value powder and solution formats alike. Big plants may need barrel shipments on a tight turnaround; we adapt to both.

    Supporting Discovery and Process Improvements

    Our years making 1-Pentyl-2,3-Dimethylimidazolium Bromide aren’t just about moving product, but advancing what’s possible for end users. By providing reliable, well-documented composition and straightforward logistics, we give everyone from bench chemists to plant supervisors a straight shot at project goals. Our QC documentation, spectral references, and technical clarification—kept up-to-date by the same team maintaining production protocols—support internal compliance and open the door to exploration and troubleshooting.

    On the application front, those working in areas like lithium battery development or ionic chromatography often need to push physical boundaries. The pentyl-substituted imidazolium cation provides more flexible design space for tuning transport properties or adjusting interfacial behavior. Instead of re-engineering existing methods for awkward chemical fits, labs drop in this salt, run their setups, and report their findings back to us. Our own technical support team integrates this user feedback directly into process improvements.

    Why Source Direct From the Manufacturer?

    Product quality starts on the line, not at the dock or sales desk. In-house control means the person who signs off on a batch knows exactly what went into it—raw material checks, environmental monitoring, and post-processing analytics. Supply chains built on personal assurance and batch documentation help overcome raw material fluctuations and nonstandard order size requests.

    Researchers who work directly with us save time tracing inconsistencies or troubleshooting protocol failures. Whether it’s a mid-sized lot for a research grant or a high-volume order timed to a production schedule, the supply remains steady. That reliability frees up time and budget for actual discovery and process development.

    Addressing the Unknowns: Safety, Handling, and Compliance

    Any ionic liquid—especially with a custom chain structure—demands care in handling. We provide succinct, evidence-backed guidance based on our own risk assessments and operator logs, not just stock phrases from generic safety sheets. Our staff who work directly with bromide- and pentyl-based intermediates train on real-world scenarios and storage conditions, giving us first-hand information to share with labs and factories. This approach reduces unplanned downtime and supports safe work practices every step of the way.

    Regular communication with regulatory bodies ensures our facility meets national and local chemical management standards. By keeping internal documentation ready for audit and taking part in industry self-monitoring programs, we keep pathways open for international shipments and short-notice custom blends.

    Moving Forward With Product Development and Collaboration

    Our experience manufacturing and supporting 1-Pentyl-2,3-Dimethylimidazolium Bromide provides a foundation for deeper work with partners across sectors. Ongoing investments in analytical instrumentation, logistics, and feedback integration mean the quality stays high and adaptable. By keeping lines open to downstream labs and pushing for honest, fact-based improvement, we make sure the advantages of this compound—clarity, adaptability, consistent behavior—translate into real outcomes for science and industry alike.

    Solutions inside the plant influence what researchers accomplish outside of it. Custom imidazolium salts like this one bridge gaps between discovery and daily use, thanks to experience honed at every stage: raw purchase, synthesis, purification, packing, and long-term support. Each bottle sent out carries the lessons of hundreds of production days and the shared stories of chemists who rely on us for progress, not just product.