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HS Code |
925788 |
| Cas Number | 419537-54-1 |
| Molecular Formula | C30H60BrN2 |
| Molecular Weight | 529.72 g/mol |
| Appearance | White to off-white solid |
| Purity | Typically ≥98% |
| Melting Point | Approximately 70-74°C |
| Solubility In Water | Moderate |
| Chemical Class | Imidazolium ionic liquid |
| Synonyms | 1,3-Bis(dodecyl)imidazolium bromide |
| Storage Conditions | Store in a cool, dry place, tightly closed |
| Boiling Point | Decomposes before boiling |
| Hazard Statements | May cause irritation to eyes, skin, and respiratory tract |
| Smiles | CCCCCCCCCCCCn1cc[n+](CC(C)CCCCCCCCCC)c1.[Br-] |
As an accredited 1,3-Didodecylimidazolium Bromide factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 1,3-Didodecylimidazolium Bromide is supplied in a sealed, amber glass bottle containing 25 grams, labeled with chemical details and hazards. |
| Shipping | 1,3-Didodecylimidazolium Bromide is shipped in tightly sealed containers, protected from moisture and light. It is transported as a non-hazardous, specialty chemical, in compliance with relevant regulations. Proper labeling and documentation ensure safe handling during transit. Store at room temperature and avoid extreme temperatures or incompatible materials during shipment. |
| Storage | **1,3-Didodecylimidazolium Bromide** should be stored in a tightly sealed container in a cool, dry, and well-ventilated area, away from moisture and direct sunlight. Keep it away from incompatible substances such as strong oxidizing agents. Use personal protective equipment when handling and ensure storage conditions maintain the chemical’s stability, ideally at room temperature or as specified by the manufacturer. |
Applications of 1,3-Didodecylimidazolium Bromide in Industrial ManufacturingAs a specialized manufacturer of 1,3-Didodecylimidazolium Bromide, we supply this ionic liquid for advanced industrial sectors requiring precise functional performance and stringent compliance. Below, we outline key downstream fields with distinct application workflows, industry standards, formulation practices, and the real-world outcomes built on this unique raw material. 1. Electrochemical Device Manufacturing: Electrolyte Formulations for SupercapacitorsIn supercapacitor production, manufacturers use this imidazolium-based ionic liquid salt as a core ingredient for advanced electrolyte systems. Its thermal stability and electrochemical window support reliable charge–discharge cycles under high current. Processing involves solubilizing the compound under inert atmosphere and integrating with conductive additives and solvent systems. Final assembly puts strict focus on purity of each batch to prevent unwanted side reactions, especially for high-energy density devices. Industry compliance standards
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2. Antistatic Additive in Polyolefin Film ProductionPlastic film processors employ this ionic liquid as an internal antistatic agent within high-density polyethylene (HDPE) and polypropylene (PP) film extrusion. Its structure allows permanent ionic mobility at the surface, suppressing static buildup crucial for electronics packaging and food contact layers. Dosage optimization remains critical to maintaining film clarity, sealability, and surface resistivity within international food safety requirements. We recommend compatibility assessments with common co-additives such as slip and anti-blocking agents in blown or cast processes. Industry compliance standards
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3. Phase Transfer Catalyst for Specialty Organic SynthesisChemical synthesis operations utilize this imidazolium bromide as a phase transfer catalyst or ionic reaction medium. Its cationic structure supports efficient transfer and activation of reactants in biphasic alkylation, esterification, and amination reactions involving organic and aqueous phases. Reaction conditions, such as pH and salt content, require adjustment to match catalyst solubility profile and target conversion rates. Scale-up from pilot to commercial production often involves batch or semi-batch process validation to maintain purity and minimize by-product formation. Industry compliance standards
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4. Surfactant in Nanomaterial Synthesis for Functional CoatingsEngineers use this ionic liquid as a capping and templating agent in the controlled growth of inorganic nanoparticles, including silver, gold, and titanium dioxide. Its dual dodecyl chains allow fine-tuned dispersion and stabilization during nucleation and particle size control, advantageous for transparent or conductive coating formulations. It enters the reaction after initial precursor mixing and remains in colloidal solution through washing steps. Residual ionic content undergoes quantification according to downstream functional and safety demands. Industry compliance standards
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At our manufacturing facility, we’ve watched the rising importance of imidazolium-based ionic liquids over the past ten years, especially in specialty chemical industries. Among them, 1,3-Didodecylimidazolium Bromide regularly generates interest for its ability to meet unique technical requirements in research, formulation, and industrial application spaces.
We produce 1,3-Didodecylimidazolium Bromide in well-controlled batches, dialing in parameters that customers rely on—purity, consistent carbon chain lengths, reliable bromide ion concentrations, and lot-to-lot reproducibility. We take every step in-house, from source chemical preparation through quaternization, to maintain oversight on potential impurities. The final material leaves our reactor with a tight, ensured purity profile, which starts with strict choice of dodecyl starting alkylating agents and thorough in-process controls.
Each molecule carries two dodecyl groups, giving the compound a strong amphiphilic character. The long C12 alkyl tails set it apart from standard short-chain imidazolium salts, influencing everything from solubility to surfactancy. The positively charged imidazolium core, balanced by a single bromide counterion, opens the door for opportunities across materials science, analytical chemistry, and biointerface design.
A key property our chemists monitor is surface activity. Shorter-chain imidazolium salts, like 1-butyl-3-methylimidazolium bromide, usually fail to deliver the interfacial performance demanded by specialty clients, especially in emulsion or conductive fluid applications. The longer hydrophobic chains of 1,3-Didodecylimidazolium Bromide drive more robust formation of micelles, vesicles, and stable emulsions. It dissolves in polar and moderately non-polar solvents, though solubility varies based on temperature and optional pre-warming.
Each production run comes with lab-verified characterization that includes NMR, water content by Karl Fischer, halide purity, and confirmation of chain length by mass spectrometry. Our team typically sees melting points in the expected range for C12 imidazolium compounds, and each batch stays fresh in the lab’s cold room until shipping.
Most requests come from customers solving interfacial chemistry challenges. This product has earned a solid reputation across several key sectors. In nanoparticle synthesis and stabilization, researchers value the ability of the imidazolium cation to modify particle surfaces, direct crystal growth, or enhance colloidal stability. Long alkyl chains form tough hydrophobic barriers on metal or oxide surfaces, which keeps nanoparticles suspended or self-assembled as required.
In electrolytes for batteries, supercapacitors, and fuel cells, this compound is chosen for its ionic conductivity and potential to tune electrochemical windows. Researchers searching for improved ionic mobility or higher charge storage densities look to these types of salts for solutions. The bromide counterion, compared to other halides, strikes a balance between ionic mobility and chemical stability in many non-aqueous media.
For the pharmaceutical sector, 1,3-Didodecylimidazolium Bromide draws attention for its role as a phase transfer catalyst or as part of formulations that require highly selective surface-active agents. Its biocompatibility and membrane permeability must be established on a case-by-case basis, but the long alkyl chains can help shuttle otherwise insoluble compounds across hydrophobic environments in synthetic and analytical workflows.
A handful of specialty coating companies lean on this compound to help organize multilayer films or to provide antistatic and antimicrobial properties. Waterborne or solvent-based coatings containing tailored imidazolium amphiphiles often display better resistance to biofouling or improved electrostatic dissipative behavior. Performance hinges on the fine details of the cation and anion choices, and our experience tells us that the twin C12 chains make a significant difference at the application interface.
Our own R&D group has tested this material in emerging applications—liquid crystalline phases, as structural templates for nanostructured materials, and in responsive gels—highlighting the unexplored directions possible with long-chain imidazolium chemistry. Our feedback loop from production staff to end-user chemists helps us improve each year, tightening up specifications as new data rolls in from the field.
In the early days of ionic liquid research, shorter alkyl chain imidazolium salts defined most of the market. Their lower cost and ready availability made them a fit for general research—but customers regularly report challenges with limited solubility in organic matrices or unstable emulsions when working with shorter chains. The extra hydrophobicity from two dodecyl groups on our product extends its range of applications far beyond commodity salts.
Cost and supply chain complexity both increase for longer-chain homologues, since dodecylbromide carries higher price volatility and the heavier molecules demand more diligent purification. We meet these demands through batch-tested process controls and decades of experience in alkylation chemistry. We keep chain length distribution minimal and bromide content high, so researchers and formulators get precisely what their application asks for without costly rework or post-purification.
We hear from polymer chemists who’ve found 1,3-Didodecylimidazolium Bromide especially useful compared to hexyl or octyl imidazolium salts, attributing improvements in phase separation, interfacial adhesion, or antistatic behavior directly to the structure of the dodecyl chains. Users tackling ionic liquid crystal research often report advances linked specifically to the amphiphilic structure, which short-chain versions cannot match. We advise on selection regularly, pointing out that each application brings its own requirements, and results often depend on a subtle match of molecular geometry, charge distribution, and hydrophobic interaction.
We watch safety data closely. Imidazolium salts can show varying degrees of toxicity and environmental persistence depending on structure. Compared with aromatic or polyfluorinated surfactants, most long-chain imidazolium bromides degrade more readily, and our team takes pride in ongoing waste reduction efforts. We run closed-process protocols to prevent any material from entering water systems; our team tests effluent before discharge and captures residuals for high-temperature incineration.
On-site, we provide robust ventilation, and operators are supplied with gloves, goggles, and respirators as recommended by regulatory standards. Personal experience teaches that powders and concentrated solutions require careful handling to ensure occupational safety. The material should not reach drains or be used in consumer products without further evaluation. We keep lines of communication open with environmental health professionals to continually learn and to maintain safe and transparent processes.
Packaging follows rigorous moisture control. The bromide salt maintains its performance better in sealed, inertized containers. We ship using gloves, dry bags, and vacuum-packed bottles for international customers who specify longer transit times. Through trial and error, we learned that with lesser packaging, customers ended up with clumpy or degraded materials, resulting in lost productivity and requalification effort.
Customers often ask about compatibility. We recommend gradual addition of 1,3-Didodecylimidazolium Bromide with stirring—unlike shorter-chain variants, this version gels or flocculates in some solvent systems, particularly at higher concentrations or in the presence of divalent cations. Our technical support team fields regular questions on co-solvent choice, mixing time, and water exclusion. Long-chain imidazolium salts demand patience and careful adjustment, but the resulting formulations often outperform those based on standard surfactants.
Batch-to-batch consistency becomes critical when scaling pilot experiments. In earlier years, broadening acceptable impurity levels led to unpredictable results for downstream users—yield drops, phase separation failures, or contaminated product slurries. Over time, we refined recrystallization and washing steps, raising spectroscopic purity and keeping halide departures below 0.1%. Customers now see tighter reproducibility in everything from conductivity testing to phase-transfer catalysis.
Reactivity with various substrates also presents a learning curve. Some users noticed reactivity between the imidazolium cation and certain nucleophiles or transition metals, particularly under high temperature. We encourage test batches with new substrates and provide guidance from our internal chemists who have run those same reactions in evaluation runs. The lessons reinforce that a good technical dialogue leads to better success rates and safer scale-ups.
Feedback shapes our evolution. Our team consults regularly with researchers developing new analytic techniques, adapting purification, or branching into new end uses such as ionic liquid crystals or soft matter assembly. These discussions push us to improve small-area NMR sensitivity, fine-tune drying procedures, and reduce residual halogens through cleaner washing and filtration.
We deliver customized lot sizes when universities run large batch tests or when an industrial partner requires a higher mass for pilot manufacturing. Our plant runs remain adaptable—while typical production scales run from grams to tens of kilograms, we have delivered everything from multi-gram research quantities up to hundreds of kilos for ongoing studies. By keeping upstream synthesis and downstream purification in-house, we maintain oversight at every critical control point.
Shipping documentation includes full traceability and a record of each quality-control test so that users never have to guess at contaminant levels or batch history. Our clients appreciate the open access to not only certificates of analysis, but also detailed spectral data, impurity analysis, and process logs. We have seen this transparency pay dividends in shorter development cycles and more confident scale-up, both in large-scale research projects and private sector runs.
Our partners share steady feedback. One biotech lab reported breakthroughs in forming stable vesicles for drug delivery, noting that switching away from a traditional, shorter-tailed imidazolium salt immediately stopped unwanted aggregation. A battery research group used our material as a conductive additive and noted improved ionic transport and less impedance vs. common tetraalkylammonium alternatives. Several coatings specialists speak highly of the surface-modifying properties, which allowed for reduced levels of antimicrobial additives and fewer rejections due to static-related film defects.
We regularly send evaluation samples for new processes—hydrotrope screening in green solvent systems, ionic-liquid templated foam creation, and solubilization of poorly behaving dyes. These collaborations often push the compound into new territory and frequently uncover solution phase behaviors that the literature has not yet documented. Student researchers, seasoned chemists, and process engineers have helped us discover unexpected miscibility, micellization, and substrate compatibility outcomes.
As the direct manufacturer, we value incremental process optimization. We have upgraded reactors for closed-system alkylations, developed improved protocols for solvent removal, and invested in in-line analytical equipment. These improvements shave weeks off purification timelines and reduce the risk of unexpected contaminant introduction—a benefit not only to us, but to the customers whose results depend on predictability.
Our technical staff stays active in the scientific community, attending conferences and collaborating with academic groups to understand new demands for high-purity ionic liquids. This effort means we spot trends to anticipate requirements, beyond the main production runs. For instance, as attention turns to energy-storage applications, we keep a reserve of analytical-grade product, dried and packed for immediate use in glovebox atmospheres. Continuous feedback from both established and new users means we can adapt production plans and upgrade our quality standards to meet rising expectations.
From synthesis through delivery, we see each batch as a partnership. We regularly host facility tours and encourage technical exchanges with customers, who bring samples back for comparative analysis or process troubleshooting. Many of the improvements we’ve adopted sprang straight from these on-the-ground interactions with partners facing nonstandard challenges—offering perspectives that can stretch even the most experienced manufacturing chemists.
Staying grounded in our craft, and connected with those who rely on 1,3-Didodecylimidazolium Bromide for their projects, gives us a unique perspective on what matters: reliability, transparency, and technical support from a producer who understands application context as well as reaction chemistry. With ongoing investment, teamwork across disciplines, and genuine curiosity about emerging uses, we continue to evolve both our product and our processes, so that each batch supports both the current demand and the next wave of breakthrough work.