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1-Dodecyl2,3-Dimethylimidazolium Bromide

    • Product Name 1-Dodecyl2,3-Dimethylimidazolium Bromide
    • Alias [C12m2im]Br
    • Einecs 629-725-8
    • 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

    844778

    Chemicalname 1-Dodecyl-2,3-dimethylimidazolium bromide
    Casnumber 298949-95-0
    Molecularformula C17H33BrN2
    Molecularweight 361.36 g/mol
    Appearance White to off-white powder
    Meltingpoint 65-70°C
    Solubility Soluble in water and organic solvents
    Purity Typically ≥98%
    Storagetemperature Room temperature, protect from moisture
    Iupacname 1-dodecyl-2,3-dimethylimidazol-1-ium bromide

    As an accredited 1-Dodecyl2,3-Dimethylimidazolium Bromide factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Sealed in a 25g amber glass bottle with tamper-evident cap, labeled with product details, hazard symbols, and storage instructions.
    Shipping 1-Dodecyl-2,3-Dimethylimidazolium Bromide is typically shipped in tightly sealed, chemical-resistant containers, protected from moisture and light. It should be handled and labeled according to hazardous material regulations. Ensure transport in accordance with local and international shipping guidelines for chemicals, including provision of the necessary safety data documentation.
    Storage **1-Dodecyl-2,3-dimethylimidazolium bromide** should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from direct sunlight and incompatible substances such as strong oxidizers. To prevent moisture absorption and degradation, keep the container tightly closed and store under an inert atmosphere if possible. Ensure proper labeling and follow all relevant safety guidelines.
    Application of 1-Dodecyl2,3-Dimethylimidazolium Bromide

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

    1-Dodecyl-2,3-dimethylimidazolium bromide serves as a functional ionic liquid and surfactant intermediate in industrial applications. The following sections detail precise downstream usages, process points, regulatory frameworks, integration methods, and final product pathways.

    1. Catalytic Phase Transfer Agent in Pharmaceutical API Synthesis

    In pharmaceutical manufacturing, this material acts as an ionic liquid phase transfer catalyst during specific quaternization and alkylation steps in active pharmaceutical ingredient (API) production. Its cationic nature enhances ion exchange and substrate activation under mild conditions, supporting efficient process yields with precise impurity control. Producers depend on it for scale-up routes of imidazole-derived APIs, ensuring consistent batch reproducibility and strict impurity profiling per regulatory demands.

    Industry compliance standards

    • Current Good Manufacturing Practice (cGMP) guidelines—FDA 21 CFR Parts 210/211
    • ICH Q7 API GMP Guide
    • European Pharmacopoeia (Ph. Eur.) requirements for residual solvents
    • US Pharmacopeia (USP) monographs for related compounds

    Typical usage ratio

    • 0.01%–1% w/w by substrate mass, adjusted based on scale and target conversion/yield profiles

    Downstream process integration

    • Introduced in the early organic synthesis stage as a phase transfer agent
    • Removed during downstream purification steps post-reaction (liquid-liquid extraction, filtration)
    • Strict monitoring for residuals in final API using validated analytical methods

    Final product types

    • Imidazole-derived APIs (antifungals, antivirals, CNS drugs)
    • Active intermediates for custom pharma syntheses

    2. Surfactant in Electrolyte Formulation for Electrochemical Devices

    Manufacturers of energy storage and conversion devices such as supercapacitors and dye-sensitized solar cells utilize this ionic material as a custom surfactant and ionic liquid component within non-aqueous electrolyte formulas. The unique structure ensures high ionic conductivity, stable interface formation, and long-term cycling durability under varying current densities. Controlled incorporation enables product-specific electrolyte tailoring for diverse device architectures and performance benchmarks.

    Industry compliance standards

    • RoHS Directive (2011/65/EU) restriction of hazardous substances
    • REACH Regulation (EC 1907/2006) for electrolyte component registration
    • IEC 62660-2 for lithium ion batteries safety and performance

    Typical usage ratio

    • 0.5%–2% w/w relative to total electrolyte mass, adjusted for specific conductivity and viscosity requirements

    Downstream process integration

    • Dissolved into electrolyte solvent blend post-drying and pre-filling
    • Maintained under controlled humidity and low-oxygen environments during cell assembly
    • Quality check by electrochemical impedance spectroscopy and purity analysis

    Final product types

    • Supercapacitor electrolyte solutions
    • Dye-sensitized and perovskite solar cell modules
    • Lithium-ion battery electrolytes for premium cells

    3. Emulsifier in Cosmetic Emulsion Bases

    Downstream personal care manufacturers utilize this cationic surfactant for stable oil-in-water emulsion formation in specialty cosmetic formulations, including leave-on creams and lotions. The long-chain imidazolium salt improves emulsion droplet size distribution, enhances product shelf-life, and enables fine-tuned texture properties. Strict regulatory review ensures only safe usage in non-rinse topical applications, with controlled levels to minimize irritation potential and ensure consumer product claims.

    Industry compliance standards

    • EU Cosmetics Regulation (EC) No 1223/2009
    • US FDA Title 21 CFR 700-740 on cosmetics safety
    • ISO 22716:2007 Good Manufacturing Practices for cosmetic production
    • Cosmetic Ingredient Review (CIR) safety assessments for cationic surfactants

    Typical usage ratio

    • 0.01%–0.5% by finished formula weight; levels finalized via stability and irritation testing

    Downstream process integration

    • Dosed directly into aqueous phase or at oil/water interface during emulsion compounding
    • Emulsification under controlled shear temperatures (40–60°C)
    • Residue testing and stability monitoring over shelf-life

    Final product types

    • Facial moisturizers
    • Lightweight sunscreens
    • Anti-aging skin creams

    4. Antistatic Agent in High-Performance Polymer Processing

    Producers of specialty thermoplastics incorporate this material as an ionic antistatic additive during the melt blending stage. The ionic liquid’s cationic surfactant properties distribute charge across polymer surfaces, reducing dust accumulation and enhancing product processability in fiber, film, and molded component production. Formulators select concentrations by measuring surface resistivity and permanence post-aging, balancing antistatic performance against mechanical property retention.

    Industry compliance standards

    • UL 94 flammability standards for plastic components
    • ISO 4892-2: Accelerated aging for plastics
    • FDA 21 CFR 177.1520 for indirect food-contact polyolefins (application permitting)
    • ASTM D257 for electrical resistivity measurement in polymers

    Typical usage ratio

    • 0.05%–0.5% w/w by resin mass, adjusted for polymer matrix and target dry surface resistivity levels

    Downstream process integration

    • Dry blended with polymer pellets prior to melt extrusion or injection molding
    • Dispersed under controlled heat and mixing to ensure uniform charge distribution
    • Tested for antistatic property persistence through real-use simulation and wear

    Final product types

    • Polypropylene and polyethylene packaging films
    • Electrical and electronics casings
    • Antistatic textile fibers for cleanroom environments
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    Certification & Compliance
    More Introduction

    1-Dodecyl-2,3-Dimethylimidazolium Bromide: A Practical Approach from the Production Floor

    Understanding Our Product

    Handling specialty chemicals in a production environment often teaches more than any catalog or textbook. 1-Dodecyl-2,3-Dimethylimidazolium Bromide stands out in our lineup because of the way it bridges proven imidazolium chemistry with modifications in the cation structure. The twelve-carbon dodecyl tail gives it a distinctive balance between hydrophobic character and solubility, making it behave differently than shorter-chain imidazolium salts or their aromatic or fused-ring cousins. Over hundreds of synthesis cycles, we have seen that this modification brings a sharper response in surfactant applications and in certain electrochemical setups, especially in lab-scale innovation as well as scale-up scenarios.

    This ionic liquid comes as a pure, flowable white to off-white solid, meeting the industry’s requirements for high assay and minimal trace ions. On our lines, we ensure a physical state that blends easily with polar and nonpolar solvents, which often gives formulators more flexibility. Storage and handling do not create specific difficulties, though as with all hygroscopic salts, dry conditions prevent caking and guarantee re-dispersion when used in blends or solutions.

    What Makes This Salt Special in Real-World Applications

    One point our operators point out—this dodecyl imidazolium bromide has a way of dispersing in water and common organic solvents that shorter chain or unsubstituted imidazolium salts do not match. Formulators come back to this material when they need a robust surfactant with strong ionic character but less tendency to form stubborn gels or cause unwanted precipitation, which often plagues comparable materials like 1-butyl-3-methylimidazolium bromide. The longer tail contributes to micelle formation, which we’ve seen reflected in clean interface formation and sharper phase separation in many test blends.

    Electrochemists who visit our plant want this salt for its unique balancing of hydrophobicity and ionic mobility. In electroplating baths and membrane research, the dodecyl and dimethyl substitution pattern gives reliable conductivity without the pronounced viscosity increase seen with some longer-alkyl ionic liquids or those with more heavily substituted rings. We consistently receive reports that our product resists electrochemical degradation over more cycles than competitors offering similar but less rigorously refined compounds.

    In direct formulations, such as in personal care, corrosion inhibition, or antifouling coatings, minor tweaks in the surfactant backbone result in product lines that perform as intended even as regulatory requirements on additives shift. Years of experience blending this material at scale have shown that its lower toxicity compared with some quaternary ammonium salts, as well as better skin compatibility, bring formulators back to it when margins don’t allow for frequent reformulation.

    The Differences That Show Up in Every Batch

    The part that most buyers miss at first is the role of substitution on the imidazole ring. The two methyl groups not only prevent certain side reactions during use, but they also increase the shelf stability of the product. We’ve tracked product performance for years, and our technical team has flagged fewer issues caused by ring-opening degradation compared to unsubstituted analogs. It lets our partners store materials for months without worrying about yellowing or off-odors that often indicate breakdown or contamination, especially when stored in less-than-ideal conditions.

    Comparing this compound to 1-dodecyl-3-methylimidazolium bromide or shorter-chain analogs points to noticeable differences in their handling. The 2,3-dimethyl version resists clumping and retains flowability, both factors that make it easier to dose in automated systems or add during continuous processing without shutdowns for maintenance. Our customers working in high-throughput blending operations appreciate the way the powder or granule form moves through feeders and silos, saving time and material.

    Production personnel regularly note that our method of synthesis creates a cleaner product: fewer colored impurities, lower levels of halide contamination, and trace metals far below common limits for performance chemicals. This comes from consistent reaction conditions, rigorous purification, and in-process monitoring, not only post-batch analysis. Over the years, we have tweaked temperatures and catalyst concentrations to get the process just right, allowing us to minimize byproducts and recycle unreacted starting materials. That helps in meeting the purity and cost expectations of the most demanding users.

    Our Day-to-Day Experience Guides Product Consistency

    Producing 1-Dodecyl-2,3-Dimethylimidazolium Bromide in-house has given us a hands-on perspective. Batch variations frustrate customers and waste time—a fact we recognized long before most specialty producers did anything about it. Our technical operators and laboratory staff keep a close eye on crystallinity and grain size during final drying and packaging. This prevents issues later in customer processing that stem from differences in surface area or solubility. This attention to detail refuses to compromise on specified moisture levels, which we routinely keep well below one percent.

    Shipping and storage matter in this specialty field, especially given the way humidity interacts with ionic liquids. Our standard packaging uses moisture-proof liners and desiccant packets sealed at the filling station, not as an afterthought. This prevents hydration and caking, and careful sealing right at the final stage gives operators downstream the confidence to move straight into production without extended drying or sieving.

    Customer feedback circles back to the way our material handles heat and agitation—no sudden softening or melting even as the process temperature rises, and no dusting that clogs environmental systems. Every production run starts with direct input from our own usage and our customers’ test results. This iterative process has moved our product profile closer to the practical needs of formulators and process chemists.

    Real Outcomes in Surfactant Systems and Research

    Academic and applied partnerships have taught us that the uniqueness of this ionic liquid lies in its compatibility with a huge range of ingredients. Where many surfactants fail to mix with nonionic or amphoteric species, our imidazolium compound persists in solution, often stabilizing emulsions and suspensions that otherwise fall apart over time. Researchers have run accelerated aging tests on our material, finding little or no phase separation over periods that would break down classic ammonium salts or unmodified imidazolium surfactants.

    Electrochemical devices and membrane science form a second area where this salt shows its strengths. As more researchers abandon older, less environmentally friendly cationic surfactants, the dodecyl imidazolium family proves it can match performance without creating persistent foam or interfering with ion transport. Reports from partner labs describe steady performance in fuel cell testing, energy storage, and water treatment setups. We’ve evaluated independent findings and validated bench results at our facility, confirming the product profile matches what truly matters at scale.

    For direct blending into commercial cleaners, paints, or antifouling coatings, this backbone brings better spreadability over surfaces and a controlled level of foaming. It resists breakdown when exposed to oxidants and withstands repeated thermal cycling, features that make a difference in shipping and storage through variable climates. These traits only emerge in side-by-side process testing, where small formulation changes open or close doors in larger scale production. Our team routinely participates in such reformulation projects, offering advice based not on theory but on repeated plant- and pilot-scale runs.

    Sustainability and Product Stewardship

    We have a responsibility to manage both the broader impacts and the immediate results of every batch we make. Recent years brought stricter regulations on surfactant residues and ionic liquid discharge. Our side chain and ring substitution have enabled partners to design formulations that break down faster in industrial and municipal waste streams. This means builders of commercial sprays and cleaning solutions can reduce or eliminate problematic persistence, a concern especially in export markets that follow European standards.

    From our point of view, traceability in raw materials and finished products goes hand in hand with stewardship. Each drum and bag receives a batch number tied to both analytical records and process notes. Every complaint or unexpected result triggers a review, not only for compliance but for root cause analysis. The production floor feeds this knowledge back to R&D and formulation support; this direct loop keeps the lab and plant talking, which makes changes in industry expectations a manageable challenge, instead of a crisis.

    Waste minimization goals impact how we operate. We recover and recycle the primary organic and inorganic intermediates. Heat exchangers and closed-loop condenser systems reduce water and solvent use, and we send no uncontrolled vapor or liquid effluent outside of tightly controlled boundaries. Larger regulatory frameworks have pushed us to stay ahead of requirements; we prefer this compliance mindset, since late-stage process changes cost more than steady improvements along the way.

    Challenges and How Experience Shaped Our Solutions

    Few manufacturers will admit that specialty ionic liquids are not always easy to crystallize at scale without forming unwanted polymorphs. Early batches sometimes formed soft chunks or greasy residues, particularly in humid conditions or with minor changes in solvent composition during crystallization. Persistent attention to solvent quality, temperature control, and efficient removal at low pressure eventually led to more reliable, granular product, even when making adjustments for seasonal humidity. This type of troubleshooting is not glamorous, but each tweak in process yields less rework and fewer complaints from users downstream.

    Handling bromide-based surfactants requires more than standard precautions. We have found that halide management, particularly in bromide recovery and waste management, prevents regulatory headaches. Decades of salt handling have shown us how ion exchange systems can purify both product and byproduct streams, pulling back expensive or environmentally sensitive ions before discharge. These closed systems now form the backbone of how we keep both cost and compliance in balance.

    End-use partners constantly face new rules and raw material disruptions. The decision to control every step of our process, rather than outsource or depend on spot-market intermediates, has shielded us from most shortages. We buy key starting materials based on verified performance and traceability, since poor quality or variable feed impacts everything that follows. Our dedication to internal quality checks, even when costly, cuts the cycle time to resolve any issues and reduces the number of non-conforming lots reaching users.

    Working with Customers and Moving Forward

    Most technical buyers and researchers want suppliers who pay attention to small details. Since we managed every part of our product’s journey, from reaction vessel to finished package, we have first-hand evidence that consistent quality lowers total cost of use. Most downstream issues arise from underappreciated variation in raw material, shipping delays, or poor packaging. Our plant team includes feedback from field personnel and customer reports in every production review.

    As trends move toward greener materials and regulations keep evolving, our team relies on practical expertise to keep product quality and compliance at the forefront. Collaborative development with downstream formulators has kept our process not only relevant but responsive. Frequent engagement with customers and hands-on trials ensure our dodecyl-imidazolium salts meet shifting needs across industries.

    Conclusion: Practical Results from the Shop Floor

    Manufacturing 1-Dodecyl-2,3-Dimethylimidazolium Bromide in-house is not just about chemistry, but about how day-to-day practices built trust in this product’s reliability. Every drum and sack that leaves our facility carries the weight of these choices: insisted-on purity, process consistency, stewardship, and the practical intelligence gained from plant experience. For partners in academia, industry, or applied research, sourcing direct from an experienced producer means fewer surprises and more support in adjusting products and processes as the world keeps changing.