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1-Propyl-2,3-Dimethylimidazolium Bromide

    • Product Name 1-Propyl-2,3-Dimethylimidazolium Bromide
    • Alias [PMIM]Br
    • Einecs 931-406-9
    • 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

    435594

    Chemical Name 1-Propyl-2,3-Dimethylimidazolium Bromide
    Molecular Formula C8H15BrN2
    Molecular Weight 219.12 g/mol
    Cas Number 73819-40-2
    Appearance White to off-white solid
    Melting Point 85-90°C
    Solubility In Water Soluble
    Density 1.32 g/cm³
    Purity Typically ≥98%
    Structure Type Imidazolium-based ionic liquid
    Synonyms [C3dmim]Br
    Storage Conditions Store in a cool, dry place, tightly closed

    As an accredited 1-Propyl-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 Sealed 25-gram amber glass bottle labeled "1-Propyl-2,3-Dimethylimidazolium Bromide"; features chemical details, hazard warnings, and supplier information.
    Shipping 1-Propyl-2,3-Dimethylimidazolium Bromide is shipped in tightly sealed containers to prevent moisture absorption and contamination. The packaging ensures chemical stability and safety during transit. Appropriate hazard labeling is applied, and handling guidelines are followed in compliance with regulatory requirements for transportation of laboratory chemicals. Store at controlled room temperature upon arrival.
    Storage 1-Propyl-2,3-Dimethylimidazolium Bromide should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from direct sunlight and moisture. Keep away from incompatible materials such as strong oxidizers. Store at room temperature and avoid exposure to heat and open flames. Ensure proper labeling, and follow local regulations for storing chemicals safely.
    Application of 1-Propyl-2,3-Dimethylimidazolium Bromide

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

    1-Propyl-2,3-Dimethylimidazolium Bromide serves as an advanced specialty ionic liquid, predominantly used in select high-end chemical, biotechnological, and polymer processing environments. As the direct manufacturer, we supply this raw material to certified industrial partners where stringent regulatory compliance and process requirements govern its use. Below, we detail its deployment across specific application scenarios, focusing on established industrial practices and technical parameters.

    1. Cellulose Dissolution and Fiber Spinning

    Industrial cellulose processing relies on ionic liquids for homogeneous dissolution, particularly in the production of regenerated cellulose fibers. 1-Propyl-2,3-Dimethylimidazolium Bromide provides high cellulose solubility and thermal stability, fitting advanced fiber spinning operations, such as those used in lyocell-type processes. This enables downstream manufacturers to bypass the use of volatile and problematic solvents, benefitting both process safety and product consistency.

    Industry compliance standards

    • OEKO-TEX® Standard 100 (applicable to end-product safety)
    • ZDHC Manufacturing Restricted Substances List
    • ISO 9001:2015 (Quality Management Systems)
    • EU REACH Regulation (registration and safe handling)

    Typical usage ratio

    • Up to 85% by mass in dissolution baths, with minor adjustments based on cellulose grade and water content tolerance

    Downstream process integration

    • Directly introduced into cellulose dissolution reactors, combined with cellulose pulp under controlled heat and agitation prior to extrusion through spinnerets

    Final product types

    • Regenerated cellulose staple fibers
    • Continuous filament yarns
    • Specialty cellulose films for packaging

    2. Catalytic Media for Nucleophilic Substitution Reactions

    Fine chemical manufacturers employ this ionic liquid as a non-aqueous medium in nucleophilic substitution reactions, taking advantage of its low vapor pressure and high ionic conductivity. It facilitates selective alkylation and halide exchange processes, improving both yields and product isolation efficiency in heterocyclic and pharmaceutical intermediate synthesis. Such use addresses solvent waste management and process safety in batch and continuous modes.

    Industry compliance standards

    • International Council for Harmonisation ICH Q7 (GMP for Active Pharmaceutical Ingredients)
    • 21 CFR Part 210/211 (US FDA cGMP requirements)
    • EU Commission Directive 2001/83/EC (medicinal products)
    • ISO 14001:2015 (Environmental Management Systems)

    Typical usage ratio

    • 30–60% of total reaction solvent volume, adjusted depending on nucleophile strength and substrate solubility

    Downstream process integration

    • Added as primary reaction medium following charger addition, maintained at precise temperature for reaction progress, followed by selective extraction and recycling protocols

    Final product types

    • Pharmaceutical intermediates, such as imidazole- and pyridine-derived compounds
    • Agrochemical precursor molecules
    • Electronic-grade organic semiconductors

    3. Electrolyte in Dye-Sensitized Solar Cell (DSSC) Assembly

    Manufacturers of thin-film photovoltaic devices employ 1-Propyl-2,3-Dimethylimidazolium Bromide as an ionic conductor in DSSC electrolyte formulations. Its low volatility and high ionic mobility enhance device durability and performance stability, addressing key longevity issues inherent in conventional organic solvents. Integration supports mass production where environmental and operational control are fundamental to module quality.

    Industry compliance standards

    • IEC 61215 & IEC 61646 (PV device testing and safety)
    • RoHS (Restriction of Hazardous Substances Directive)
    • ISO 14001:2015 (Environmental Management Systems)
    • REACH registration and safety dossier (ionic liquid disclosure)

    Typical usage ratio

    • 15–25% by mass of the total electrolyte solution, adapted based on viscosity and target ionic conductivity

    Downstream process integration

    • Dispersed with iodine or other redox mediators into electrolyte solutions in a controlled atmosphere; filled into module cells prior to sealing and final curing

    Final product types

    • Flexible photovoltaic modules
    • Building-integrated photovoltaic (BIPV) panels
    • Portable DSSC chargers for consumer electronics

    4. Solvent for Biocatalysis and Enzyme Stabilization

    Industrial biotechnology processes require stable, non-denaturing solvents for enzymatic transformations, particularly where water-sensitive substrates are involved. Our ionic liquid proves effective for immobilizing and stabilizing lipase, cytochrome P450s, and other biocatalysts, fostering enhanced conversion rates and recyclability in biosynthesis of fine chemicals and nutraceuticals. Controlled solvent polarity and low toxicity for enzyme systems underscore its adoption in GMP-compliant production suites.

    Industry compliance standards

    • European Pharmacopoeia (Ph. Eur.) guidelines for enzyme and excipient safety
    • USP <1072> Excipient biological safety
    • ISO 13485:2016 (Medical device / enzyme handling)
    • GMP (Good Manufacturing Practice) for bioprocessing

    Typical usage ratio

    • 5–30% by volume in reaction mixtures, adjusted by enzyme type and substrate hydrophobicity

    Downstream process integration

    • Blended directly into bioreactor charge alongside buffer and co-factors; maintained under isothermal, low-shear agitation to achieve maximum conversion and product recovery

    Final product types

    • Chiral fine chemicals for pharmaceutical synthesis
    • Enzyme-derived food supplements
    • Specialty aroma compounds

    5. Conductive Additive in Solid Polymer Electrolytes

    High-performance battery manufacturers integrate this ionic liquid into solid polymer electrolyte matrices to increase ionic transport and molecular flexibility. Its compatibility with lithium and sodium salt systems reduces phase separation and supports stable cycling performance in next-generation battery applications. Strict material control and proprietary compounding technology ensure consistency for safety-critical energy storage devices.

    Industry compliance standards

    • UN 38.3 (Safety testing for lithium batteries)
    • IEC 62660-2 (Secondary lithium-ion cells for automotive applications)
    • UL 1973 (Stationary battery safety)
    • REACH pre-registration for additive use in energy devices

    Typical usage ratio

    • 3–10% by mass in polymer electrolyte blends, with precise dosing matched to target conductivity and mechanical strength requirements

    Downstream process integration

    • Introduced during melt compounding or in situ polymerization of electrolyte layers in the battery assembly line

    Final product types

    • Lithium-ion pouch cells
    • Solid-state battery modules
    • High-safety backup power cells
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    Certification & Compliance
    More Introduction

    1-Propyl-2,3-Dimethylimidazolium Bromide

    A Closer Look at a Tailored Imidazolium-Based Ionic Liquid

    In our facility, experience shapes every batch of 1-Propyl-2,3-Dimethylimidazolium Bromide that comes off the line. The details matter from raw materials to finished bottles. For manufacturers and researchers looking to fine-tune their processes, this compound stands out because of specific properties rooted in its structure. Over the years, our technical team has seen how the propyl and dual methyl groups bring out particular behaviors in solvent power, melting points, and chemical compatibility. Not every ionic liquid responds the same way in a chemical procedure or a formulation. Precision in synthesis and attention to every purification step go a long way, and that's visible in the results our partners achieve.

    Model and Specifications: Precision Drives Every Step

    Our process with 1-Propyl-2,3-Dimethylimidazolium Bromide centers on reproducibility and purity, not batch volume or cost shortcuts. The C3 propyl chain on the imidazolium ring—combined with the methyl groups at the 2 and 3 positions—affects the viscosity and thermal window. We see labs and industrial groups push for consistent lots because unpredictable properties ripple through scale-up. Purity checks use NMR and ion chromatography, which spot even the faintest starting material residues or cross-contamination from nearby imidazolium products. What comes out meets high purity marks, and that makes a difference when reaction conditions sit on tight margins.

    For specifications, the recorded melting point stands higher than butyl-substituted imidazolium salts, with a solid-state stability preferred in some applications. Water content and residual solvents get minimized through vacuum and controlled atmosphere drying. We stick closely to this—having once watched a kilolab batch take three times as long to dissolve in an organic system than anticipated, just because water traces hovered above 0.2 percent. Avoiding nitrogen bases that leach out colored byproducts matters as much as tweaking the drying steps. Sometimes the solution to a stubborn discoloration problem came down to reviewing the drying column material.

    Why Laboratories and Industry Turn to This Product

    Processing habits carry from academic benches to production lines. We’ve noticed that chemists favor this imidazolium salt when they need tailored solvation and cleaner separations. In synthesis, it serves as a solvent or co-solvent that sidesteps some hazardous organics and improves phase behavior in ionic liquid extractions. The propyl and methyl arrangement alters cation-anion interactions and interfaces with metallic species or organocatalysts, which shows up in selectivity and speed. Electrochemical applications use it for its wider electrochemical windows compared to shorter-chain analogs. Minor variations at the ring positions give real shifts in physical behavior and chemical compatibility, which some of our long-term partners learned through side-by-side runs.

    Organic synthesis does not always benefit from generic solvents. We saw higher yield and selectivity improvements in alkylation and Suzuki couplings when 1-Propyl-2,3-Dimethylimidazolium Bromide replaced conventional solvents. In the lab, a lead chemist demonstrated that the melting point and ionic mobility strike a balance the butyl-analogues miss, especially at moderate temperatures. This changes how reactions run, speeds up isolation steps, and eliminates a few workup headaches. Using this product ends up less about simply meeting minimal requirements and more about unlocking a path to better throughput and precision, especially in multi-step synthesis flows.

    Switching to this salt for electrolytic applications led engineers to report more consistent current densities and lower volatile emissions. Each time a new use case shows up in technical discussions, we lean into our batch records to see which small tweaks made a difference the last time around. We keep up the documentation because repeat issues almost never come down to the big, obvious differences but rather the overlooked handling or purification step.

    Comparing to Other Ionic Liquids

    No two imidazolium salts act completely alike. We manufacture a range of these compounds, and the differences lead to practical results in the field. For example, 1-Propyl-2,3-Dimethylimidazolium Bromide does not simply follow the same melting point trend as the commonly used 1-Butyl-3-methylimidazolium analogs. Side-by-side measurements showed a distinct increase in thermal stability, muting transitions that would complicate batch processes relying on phase changes. On the bench, that stability means less glassware replacement, lower risk of side degradation, and more predictable product yields.

    The cationic structure in this molecule creates less tendency for water uptake compared to ethyl or butyl chain homologues. This catches some routine users off-guard on first switch, as some standard drying protocols overshoot and lead to unnecessary waste. Our own early process data confirmed that over-drying brought losses without additional benefit. Solid residue persists at slightly elevated temperatures, which changed our controlled delivery protocols after observing inconsistent dosing in a flow reactor. Each lesson comes directly from experience, not just theory—our staff tracks which products demand which adjustments on the line.

    In solvent extraction, phase separation speeds differ. This compound brings a measured hydrophobic/hydrophilic balance absent in its shorter or longer-chain kin. Plant operators told us that using the product sped up clarification phases and improved the purity of target fractions. Over time, even the smallest cuts in purification cycles add up to tangible efficiency gains across large volumes. We've watched months where switching a single intermediate meant less downtime for filtration and less solvent recovery burden.

    Other areas, like catalysis, benefit from the non-trivial shift in electron density around the imidazolium ring. Metal-catalyzed reactions and enzyme stabilization both trace subtle improvements to this compound’s structure. Electrolyte stability in prototype energy devices persisted longer in stress testing when using this salt compared to more basic imidazolium variants. The methyl and propyl configuration blocks sites for unwanted reactivity, which chemists and materials engineers both noticed in the form of lengthened cycle lives and fewer system fouls in electrochemical stacks.

    Each of these performance shifts only became clear after tracking hundreds of hours of pilot and plant data. There’s no shortcut to understanding how a given formula will react to an operational change. The differences don’t all show up in a spreadsheet or a datasheet; sometimes real benefits only reveal themselves after enough run cycles dial in the parameters and surprises shake out. Our team watches use case feedback closely and feeds every new result directly into the next round of process development.

    Ongoing Challenges and Solutions from the Manufacturer’s Perspective

    Manufacturing this compound to high standards raises real-world issues, from scale-up bottlenecks to regulatory scrutiny. A key challenge comes down to purification at scale. As production moved from multi-kilogram to ton runs, certain byproducts, undetectable in R&D-scale lots, showed up and demanded new separation steps. Our QC group worked out staged, in-line purification with solvent swaps to clear those trace impurities before bottling, something that would have been impossible without committed batch record-keeping and close communication between groups.

    Water management presents another ongoing issue. Atmospheric humidity shifts—especially across seasons—caused us to reset environmental controls to keep product within narrow specifications. Small changes in water content influenced melting points and solution behavior. Once, a logistics delay exposed product to unconditioned warehouse air, and recalibrating drying loads fixed the resulting performance hit. It pays to align packing protocols with actual shipping realities, and we adjusted our shipment planning to avoid repeated excursions.

    Another persistent problem surfaced in the interaction with container materials. Small-molecule ionic liquids can extract plasticizers from some packaging types. We phased out certain high-molecular-weight polyethylenes after observing leachate issues in early stored batches. Stainless and borosilicate now handle most product containers, confirmed by mid-term stability checks. Even the most robust QMS systems do not predict every practical outcome, but integrating rapid feedback from the floor shortens resolution times every year.

    In markets where regulatory and environmental compliance grow tighter year over year, transparent documentation and traceability have gone from nice-to-have to essential. Our tracking systems meet and, in places, exceed standard expectations. We maintain batch histories back to root reagents to answer audits and collaborator queries. Many new customers vet supplier documentation before a single order—every week brings another set of requests for chain-of-custody proof, and our team has grown adept at meeting those standards without bottlenecking internal flows.

    For decades, our approach favored single-source, closely monitored supply for all inputs. This avoided quality problems seen by facilities running with more price-sensitive sourcing. Several phases of feedstock tightness—including one recent disruption tied to upstream bromide shortages—confirmed that robust procurement pays off even during sector-wide supply stress. We never watered down our minimum batch sizes or substitute critical precursors. Sourcing reliability means customers do not suffer mid-project substitutions, a problem that’s both expensive and easily avoidable for manufacturers willing to plan for the unexpected.

    Conversations with Users: Continuous Improvement on Both Sides

    Our technical support lives in constant contact with users. Out in the field, it’s not theory that rules but the immediate, practical result. Feedback sometimes exposes a process gap we did not catch in-house. On several occasions, custom purifications or packaging changes arose because a research group documented new degradation pathways or a production plant documented uneven solution viscosity in a controlled process environment. Each request runs through pilot batches before implementation, and improvements usually end up feeding our standard practice.

    We keep every product launch and revision rooted in direct application testing. One memorable collaboration with a pharmaceutical chemist led to reevaluating trace metal tolerance in the finished compound, prompting a shift in purification solvent choice. In more than half the improvements now standard in our lot release, customers played a role—either by sharing surprising results from their advanced applications or reporting small but consistent yield variation when minor quality shifts went unnoticed.

    Some partners run programs that continually cycle between pilot and full process, changing one parameter at a time. This feedback teaches us how minute changes in density or viscosity alter output or clean-up downstream. We saw one application cut a full hour from reaction time just from optimizing the water content in a single upstream step. Every efficiency gain may look small in isolation but stacks up to sizable improvements in revenue or result clarity over a year’s run.

    There’s another layer in field feedback: operator experience. Despite automation's spread, operator familiarity with a color, smell, or texture change often marks the first sign of a process drift. Our documentation now incorporates non-numeric quality control points—reflecting the reality that experienced staff catch consumption rate shifts or subtle viscosity changes that no probe could immediately confirm. These details enter incident logs for review across all teams, closing a loop that keeps quality high and drift low.

    Supporting R&D and Commercial Production: Beyond Product Supply

    We see our job as reaching beyond simply filling bottles and pallets. Supporting users with application data, regulatory assistance, and process troubleshooting defines long-term supply stability. More laboratories and plants bring up integration of new ionic liquids into a legacy workflow every season, and technical know-how separates a smooth transition from a rough one.

    One output of this support comes in our real-time guide to troubleshooting common reaction, extraction, and storage hurdles seen with 1-Propyl-2,3-Dimethylimidazolium Bromide. It wasn’t enough to send out a batch and wait for an email. We supply reference procedures for most common failure points: incomplete dissolution, crystallization out during scale-up, or container compatibility questions. SOPs frequently get tweaked to mirror best practices found through troubleshooting. Each adjustment directly links to gaps seen on the customer end.

    Environmental and regulatory regimes keep raising the bar for documentation and process transparency. Our established chain-of-custody records and process logs let research groups and production leads pass audits with less disruption. We regularly supply water content data, batch impurity levels, and trace origin certifications well beyond regulatory mandates. This has shortened many a project’s regulatory review period, saving real time in time-to-market for new chemical entities.

    In teaching institutions and research centers, direct support for handling and safe disposal has also become key. Questions rarely stop at the initial spec but branch out to method optimization and end-of-life waste management. Our staff compiles best practices from around the world, updating process and laboratory recommendations monthly to keep up with both innovation and shifting national regulations.

    Continuous Learning Keeps Quality on Course

    Experience, not formulae alone, keeps our product quality where it needs to be. Every adjustment—new drying steps, material sourcing, handling SOPs—came from solving a real, observed problem. Customer partnerships, responsive process monitoring, and data-driven improvements have shaped what our 1-Propyl-2,3-Dimethylimidazolium Bromide delivers today. We never assume one protocol stays valid forever and always keep an open line for field feedback. That stance, rooted in daily work and ongoing collaboration, sustains both performance and partnership. Chemical manufacturing rewards attention and adaptation, and we hold that standard at every stage of the journey.