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1-Butyl-2,3-Dimethylimidazolium Iodide

    • Product Name 1-Butyl-2,3-Dimethylimidazolium Iodide
    • Alias [BMMIM][I]
    • Einecs 613-531-7
    • 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
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    Specifications

    HS Code

    230676

    Chemical Name 1-Butyl-2,3-Dimethylimidazolium Iodide
    Cas Number 123365-22-0
    Molecular Formula C9H17IN2
    Appearance White to off-white solid
    Melting Point 122-124°C
    Solubility Soluble in water and polar organic solvents
    Density 1.52 g/cm³ (approximate)
    Purity Typically ≥98%
    Storage Conditions Store at room temperature, in a tightly closed container, protected from light and moisture
    Synonyms BMIM Iodide; 1-Butyl-2,3-dimethylimidazolium iodide
    Smiles CCCCn1c(C)nc(C)n1.[I-]

    As an accredited 1-Butyl-2,3-Dimethylimidazolium Iodide 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-Butyl-2,3-Dimethylimidazolium Iodide is packaged in a clear, sealed glass bottle with a secure screw cap.
    Shipping **Shipping Description:** 1-Butyl-2,3-Dimethylimidazolium Iodide is shipped in sealed, chemical-resistant containers to prevent moisture ingress and contamination. It is transported as a non-hazardous material under normal temperature conditions, following standard regulations for chemical reagents. Handling precautions include avoiding direct contact and storing away from strong oxidizers and incompatible substances during transit.
    Storage 1-Butyl-2,3-dimethylimidazolium iodide should be stored in a tightly sealed container, in a cool, dry, well-ventilated area, away from moisture, heat sources, and direct sunlight. Keep away from incompatible substances such as strong oxidizers. Store under inert atmosphere if sensitive to air or moisture, and label the container clearly. Ensure proper safety procedures and personal protective equipment during handling.
    Application of 1-Butyl-2,3-Dimethylimidazolium Iodide

    Applications of 1-Butyl-2,3-Dimethylimidazolium Iodide in Industrial Manufacturing

    1-Butyl-2,3-Dimethylimidazolium Iodide serves as a specialized ionic liquid for advanced chemical processes. As an integrated chemical manufacturer, we supply this material to downstream partners working in energy conversion, pharmaceutical synthesis, catalysis, and materials science. The following sections detail key industrial applications, relevant standards, application techniques, and end-use product categories.

    1. Electrolytes for Dye-Sensitized Solar Cells (DSSCs)

    Downstream manufacturers adopt 1-Butyl-2,3-Dimethylimidazolium Iodide as an iodide source and conductive medium in advanced DSSC electrolytes. Its high ionic conductivity and thermal stability support stable photoelectric conversion. Production engineers ensure purity and moisture content to meet cell longevity requirements, while R&D teams adjust cation composition to target device efficiencies.

    Industry compliance standards

    • IEC 60904-1-2 (Photovoltaic device testing)
    • REACH Regulation (EU 1907/2006) chemical safety registration
    • RoHS Directive (2011/65/EU) for Hazardous Substances
    • ISO 9001:2015 Quality Management in device fabrication

    Typical usage ratio

    • Employed at 0.2–0.8 M in organic solvent-electrolyte mixtures for lab and commercial cell assembly
    • Engineers optimize concentration based on device architecture, target voltage, and electrolyte viscosity

    Downstream process integration

    • Dissolved into acetonitrile or propylene carbonate with co-iodides and additives
    • Filtered for particulates before cell injection
    • Sealed directly inside cell modules, followed by precision QC of ionic conductivity

    Final product types

    • Dye-sensitized solar cell panels
    • Flexible photovoltaic modules
    • Consumer solar chargers
    • Building-integrated photovoltaics (BIPV) glass

    2. Organic Synthesis as Phase Transfer Catalyst

    Process chemists use this imidazolium salt as a phase transfer catalyst in nucleophilic substitutions, oxidations, and halide exchange reactions. The cation structure enables selective activation and transfer of iodide ions, especially in biphasic systems where standard catalysts underperform. Manufacturing operations control temperature and agitation for reaction completion and post-reaction separation.

    Industry compliance standards

    • IPEC GMP Guidelines for active pharmaceutical intermediate (API) processing
    • 21 CFR Part 211 for pharmaceutical production (where downstream used in APIs)
    • OECD Guideline 123 for chemical safety during synthesis
    • ISO 14001 compliance for chemical emissions management

    Typical usage ratio

    • Phase transfer catalyst loading ranges from 1–5 mol% relative to limiting substrate
    • Lab and pilot engineers adjust ratio based on solvent polarity and scale

    Downstream process integration

    • Combined in reaction flask with aqueous and organic phases
    • Dosed at the beginning to initiate ion transfer between layers
    • Recovered by extraction or distillation after product isolation

    Final product types

    • Specialty organic intermediates
    • Pharmaceutical building blocks
    • Agrochemical active ingredients
    • Halogenated fine chemicals

    3. Catalytic Media in Carbon Dioxide Fixation

    R&D departments employ our imidazolium iodide as an ionic medium in catalytic conversion of CO2 with epoxides or aziridines to cyclic carbonates and ureas. Its chemical structure facilitates nucleophilic activation of CO2 and stabilizes intermediates, allowing for lower reaction temperatures and selective product profiles. Quality control tracks water content and halide purity to prevent catalyst poisoning.

    Industry compliance standards

    • ISO 9001:2015 for catalyst component traceability
    • REACH compliance for chemical use in European facilities
    • Responsible Care® chemical management
    • Process Safety Management (OSHA 1910.119) for large-scale systems

    Typical usage ratio

    • Used as 5–10 mol% vs. epoxide feedstock in batch and continuous reactors
    • Chemical engineers fine-tune based on catalyst recycling and conversion rates

    Downstream process integration

    • Mixed in-situ with CO2, metal complexes, and substrate under mild pressure
    • Maintained via recirculating loop to minimize raw material loss
    • Separated and regenerated alongside product purification steps

    Final product types

    • Cyclic carbonates for lithium battery electrolytes
    • Dimethyl carbonate and propylene carbonate for solvent industries
    • Non-isocyanate polyurethanes (NIPUs)
    • Urea derivatives for plastics and resins

    4. Ionic Liquid Electrolytes for Supercapacitors

    Leading supercapacitor manufacturers integrate our product in high-voltage devices as a non-volatile, thermally-stable ionic liquid electrolyte. The molecule enables stable electrode performance at elevated temperatures and over extended cycles. Production teams combine with organic solvents or directly employ neat in symmetric or hybrid EDLC assembly, following strict material purity checks.

    Industry compliance standards

    • IEC 62391-1 for Electrochemical Capacitor performance
    • UL 810A electrical safety for capacitors
    • ISO/TS 16949 for automotive electronics
    • RoHS Directive for non-hazardous materials in electronics

    Typical usage ratio

    • Applied as main electrolyte or in 50–90% wt/wt blends with organic solvents
    • Adjustments based on target capacitance, ESR, and operational temperature range

    Downstream process integration

    • Introduced during wetting of electrode/separator stacks
    • Sealed within assembled supercapacitor units under inert conditions
    • Validation through impedance testing after electrolyte filling

    Final product types

    • Automotive energy storage modules
    • Consumer-grade ultracapacitors
    • Industrial backup power capacitors
    • Grid frequency regulation devices
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    Certification & Compliance
    More Introduction

    Introducing 1-Butyl-2,3-Dimethylimidazolium Iodide: A Versatile Ionic Liquid

    Our Direct Experience with 1-Butyl-2,3-Dimethylimidazolium Iodide

    In our production lines, 1-Butyl-2,3-dimethylimidazolium iodide often turns up as one of the more reliable and flexible ionic liquids we synthesize. Chemists recognize imidazolium-based ionic liquids for their stability and tunable properties, but the 2,3-dimethyl modification gives this product a unique place among its peers. We develop this compound with a focus on batch consistency and high purity, which matters deeply for customers working with sensitive applications, especially in electrochemistry and organic synthesis.

    Our manufacturing processes involve careful alkylation and methylation steps, verified by both analytical and functional bench tests. Throughout these stages, hands-on attention improves reproducibility. The iodide counterion in this salt provides measurable differences in conductivity and redox behavior compared to the more common chloride or tetrafluoroborate options, a point that grows critical with applications like dye-sensitized solar cells, where electron transfer and stability set boundaries on device efficiency.

    Through years of feedback from advanced materials researchers and battery developers, we’ve seen the demand for this specific formulation grow. Early on, a few customers mentioned how the viscosity, lower than the bis(trifluoromethanesulfonyl)imide variants, helps with solution handling and process throughput. We've even taken direct samples from synthesis runs to measure viscosity and density ourselves, checking against published data and tightening our in-process controls. Our experience shows that trace moisture removal and precise temperature control during the final purification step keep the physical properties in line with customer expectations, and more importantly, their reproducible lab results.

    Specifications that Matter in Daily Work

    We manufacture 1-butyl-2,3-dimethylimidazolium iodide (CAS 211135-40-5) as a white to off-white crystalline solid. During scale-up, our team tracks melting point, purity by HPLC, and stable color—these tangible checkpoints translate into process predictability for technicians and researchers using the product downstream. Based on market requests and direct consultation with research labs, our main packaging options cover a spread from grams to multi-kilogram containers, all sealed to limit ambient humidity uptake. Customers in fields like organic photovoltaic development or electroanalytical chemistry have repeatedly shown that starting with a consistently high-purity product removes unnecessary troubleshooting further along in their work.

    Where product consistency really pays off comes during reaction optimization and device assembly. Even minor fluctuations in purity can alter charge transfer rates or electrode stability. Through repeated hands-on syntheses, our chemists have adjusted timings, solvents, and crystallization protocols, making sure every batch aligns with the performance metrics customers relay back to us. Direct communication with downstream users often exposes subtle differences in solubility or electrochemical window, allowing us to adjust parameters and track the changes against real-world application data.

    Lab users often reach out for advice on storing and handling the material. Freshly opened containers reveal a free-flowing powder, but exposure can cause caking if not managed well. To address this, we've worked on improving package seal integrity and even trialed small inert-atmosphere sample packs. Storage at room temperature away from direct sunlight prevents decomposition, an observation confirmed by routine stability tests in our in-house quality labs. Technicians performing high-sensitivity measurements usually dry the compound under vacuum—an experience mirrored by our own staff when running in-house physical property measurements.

    Common Uses Backed by Real-World Feedback

    The most exciting part of producing this ionic liquid sits with how broad its appeal has grown. Originally, we made small batches primarily for university groups investigating alternative electrolytes. Over the past decade, interest shifted strongly towards renewable energy systems. 1-butyl-2,3-dimethylimidazolium iodide has found repeated use as an electrolyte component in dye-sensitized solar cells, where the focus on stable long-term performance and non-volatility aligns perfectly with its properties.

    Battery researchers working with advanced lithium systems frequently order this compound for its favorable ionic conductivity and the manageable viscosity profile, compared to some other imidazolium salts. Conversations with engineers in these sectors reveal they appreciate the absence of halogenated side products and the compound's compatibility with a wide set of cathodic and anodic materials. It stands up well in various electrode formulations, which reduces the time spent screening for unwanted side reactions.

    Organic synthesis teams have leveraged its ionic character to run catalytic transformations and solvent-free reactions. The methyl groups at the 2,3-position confer extra steric protection, which can affect catalytic selectivity in both established and exploratory protocols. Our factory chemists have run pilot studies side-by-side with standard imidazolium iodide salts and noticed the difference in phase behavior, supporting researchers experimenting with unique solvent/catalyst systems.

    Real Differences from Other Imidazolium Salts

    During manufacturing, we notice distinct differences between 1-butyl-2,3-dimethylimidazolium iodide and more common structures such as 1-butyl-3-methylimidazolium iodide or 1-ethyl-3-methylimidazolium iodide. The extra methyl group changes the central ring's electron density, leading to shifts in melting point and thermal stability. This subtle modification tweaks both the fluidity and the compatibility with sensitive catalytic species.

    In practice, this means the 2,3-dimethyl substitution leads to improved hydrolytic stability. Labs working with moisture-sensitive processes or hygroscopic intermediates benefit from the additional methyl shielding, which we’ve confirmed through internal hydrolysis trials and comparison studies. Less decomposition leads to fewer colored impurities, something frequently reported back by customers after switching from less substituted analogs. Our team records differences in electrochemical windows during quality control checks, and researchers have documented higher electrochemical stability limits in specific applications.

    Another difference involves the interaction with iodine in redox shuttles. Dye-sensitized solar cell developers prefer the 2,3-dimethyl variant as it can reduce volatility while improving charge transport across the cell. Direct feedback led us to modify our synthetic protocol to tighten control over trace impurities, because even minor shifts affected device lifespan. These insights arose through communication with application engineers performing accelerated aging, confirming that extra methylation delivers tangible downstream benefits.

    Rapid dissolution in polar organic media comes up regularly, especially compared to bulkier counterions. Our plant technicians notice how quickly this salt forms clear solutions even at high concentrations, easing sample prep and scale-up. Most alternative imidazolium salts lag behind in this aspect, with cloudiness or solids appearing in certain solvent systems. Our production teams adjust reactive steps to maximize solubility and minimize byproduct formation, drawing on a decade of cumulative synthesis experience.

    Supporting Innovation with Genuine Supplier-User Collaboration

    Running a manufacturing facility means we see the daily push for new materials that bridge the gap between limited lab-scale discoveries and real products. Our work with 1-butyl-2,3-dimethylimidazolium iodide increasingly involves joint development with end-users. Energy device prototyping, new organic transformations, specialized analytical methods—these collaborations reveal what properties matter most on the ground, not just on paper.

    Occasionally, our technical staff visits partner labs to see devices assembled with our chemicals or helps troubleshoot unexpected results. Hands-on cooperation reduces errors and leads to new application ideas. Quantitative feedback about thermal drift during cycling, changes in electrode adhesion, or even subtle color shifts in the finished product helps us fine-tune purification steps and shipping conditions. Any material irregularity detected through this cycle flows straight back to our process engineering and quality control teams.

    Researchers developing new electrolytes for redox flow batteries recently pointed out that rapid delivery and reliable documentation shaped their ability to publish reproducible results. Working on-site with these groups taught us the importance of transparent batch-specific testing data, so now we include full NMR, water content, and ionic conductivity panels for every delivered batch. This completeness has closed the loop on uncertainty for several longstanding customers, many of whom have shared post-publication data supporting the use of our product in high-impact applications.

    Hands-on Solutions for Supply and Technical Challenges

    Supply interruptions or inconsistent batches don’t help anyone. We noticed, especially during global logistic constraints, that steady manufacturing and flexible packaging matter just as much as the underlying chemistry. Our operations group worked through raw material substitutions and solvent recovery tweaks over the past few years, ensuring sustained supply without sacrificing quality. Every modification sees direct confirmation by both in-house and external laboratory panels.

    Trace impurity levels—like halides or residual solvents—challenge many producers of ionic liquids. We invested in recent years to expand in-line analytical checks, including ion chromatography and advanced spectroscopic methods. A deeper focus on these tangibles gave our customers greater confidence, and we accelerate product release when quality hits or exceeds specification. Internal reporting links impurity control directly with improved device output, an outcome we see mirrored in journals publishing solar, battery, or catalysis results based on our batches.

    User safety and compliance play an increasing role, with regulatory scrutiny climbing each year. Any change in global guidelines ripple through both our processes and client documentation. We now send updated (and product-specific) hazard and handling guidance along with every shipment, reflecting ongoing dialogue with occupational health specialists using our chemicals on the shop floor. Ongoing audits at our facility reinforce the focus on containment, worker training, and transparent communication around any observed process deviation.

    Continuous Improvement through Experience

    Manufacturers see more than just the bottle on the shelf or the invoice page. Direct experience with global supply lines, chemical behavior in scaled reactors, and extended conversations with end users shape how we improve the materials themselves. The journey with 1-butyl-2,3-dimethylimidazolium iodide illustrates this: from technique updates to packaging overhauls, every adaptation ties back to practical realities observed inside and outside our plant.

    End-users developing embedded electronics or heat-stable coatings recently requested custom moisture specifications. It took several months for our line operators and chemists to dial in the necessary drying cycle and verify the data, but the result gave customers a new window of process stability and throughput. This kind of incremental but sustained improvement underlines why keeping feedback channels open with active researchers, technicians, and quality managers defines how a manufacturer can add value outside of simple supply.

    We rarely see a static demand profile for specialty chemicals, and 1-butyl-2,3-dimethylimidazolium iodide is a strong example of a product that adapts with evolving market and research needs. Our direct knowledge, built from both successful and challenging production runs, collaborative troubleshooting in customer labs, and a relentless pivot toward higher quality, sets the standard for how we continue supporting innovation.