|
HS Code |
174884 |
| Chemical Name | 1-Butyl-2,3-Dimethylimidazolium Chloride |
| Cas Number | 244193-56-4 |
| Molecular Formula | C9H17ClN2 |
| Molar Mass | 188.7 g/mol |
| Appearance | White to off-white solid |
| Melting Point | 93-97°C |
| Boiling Point | Decomposes before boiling |
| Solubility In Water | Highly soluble |
| Density | 1.04 g/cm³ (approximate) |
| Storage Conditions | Store in a cool, dry place, tightly closed |
| Smiles | CCCCn1c(C)nc([N+](C)=C1)Cl |
| Purity | Typically ≥98% |
As an accredited 1-Butyl-2,3-Dimethylimidazolium Chloride factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Sealed 100g amber glass bottle with tamper-evident cap, labeled “1-Butyl-2,3-Dimethylimidazolium Chloride” with hazard pictograms and handling instructions. |
| Shipping | 1-Butyl-2,3-Dimethylimidazolium Chloride is shipped in sealed, chemical-resistant containers. It should be transported under cool, dry conditions, away from incompatible materials. Proper labeling and documentation are required, following relevant regulations. Handle with care to prevent damage or leaks. Ensure compliance with safety guidelines for chemical transportation. |
| Storage | Store 1-Butyl-2,3-Dimethylimidazolium Chloride in a tightly sealed container, away from moisture and incompatible substances such as strong oxidizers. Keep in a cool, dry, and well-ventilated area, protected from direct sunlight and sources of ignition. Use appropriate personal protective equipment when handling, and store at room temperature. Ensure proper labeling and follow local regulations for storage of chemicals. |
Applications of 1-Butyl-2,3-Dimethylimidazolium Chloride in Industrial ManufacturingAs original manufacturers, we support chemical processors and manufacturers by supplying high-purity 1-Butyl-2,3-Dimethylimidazolium Chloride (BDMIM-Cl) for technically demanding applications. Below, we outline commercial downstream uses, emphasizing proven sectors, specific process integration, compliance, and output types. 1. Cellulose Dissolution for Specialty Fiber Spinning1-Butyl-2,3-Dimethylimidazolium Chloride acts as a direct cellulose solvent for regenerative fiber manufacturing, such as spun-based cellulosic yarns. In this pathway, BDMIM-Cl replaces volatile organic solvents in dissolving pulp processing, enabling homogeneous cellulose solutions at controlled temperature and viscosity. Spin-dope parameters allow precise fiber property modulation. The textile industry adopts this ionic liquid route to reduce emissions and meet environmental safety mandates. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
2. Catalytic Media for Transition Metal-Catalyzed Organic SynthesisBDMIM-Cl serves as an engineered ionic liquid medium enhancing solubility and selectivity for homogeneous catalytic reactions in active pharmaceutical ingredient (API) intermediates and fine chemicals synthesis. Its unique ion pairing and low volatility provide superior control over catalyst activity and product isolation, specifically in Pd-, Ni-, and Ru-catalyzed couplings and reductions. The compound allows for catalyst recycling while minimizing hazardous solvent output. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
3. Electrolyte Additive for High-Energy-Density BatteriesIn energy storage device assembly, BDMIM-Cl acts as a co-electrolyte or additive in both lithium-ion and sodium-ion battery systems, particularly in research and pilot-scale solid-state and hybrid cell designs. Its low volatility, high ionic conductivity, and thermal stability boost electrochemical stability windows, improve electrode interface formation, and suppress dendrite growth for extended cycle lifetimes. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
4. Solubilizing Agent in Enzyme-Based Biomass ConversionIndustrial biorefinery processes use BDMIM-Cl to enhance enzymatic access during lignocellulosic biomass saccharification. The ionic liquid disrupts hydrogen bonding in plant cell walls, optimizing substrate swelling and reducing recalcitrance. This supports elevated conversion rates in enzyme-catalyzed hydrolysis, reducing enzyme demand and shortening batch cycles for fermentable sugar production, particularly in second-generation biofuel operations. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
5. Solvent System for Nanomaterial Dispersion and ProcessingIn advanced material manufacturing, BDMIM-Cl functions as a dispersion and stabilization medium for nanomaterials like graphene, carbon nanotubes, and metal nanoparticles. Its high polarity and thermal stability allow effective exfoliation and prevent aggregation during mixing and deposition, supporting precise coating, film casting, and electrode fabrication in electronics and conductive composites. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
|
Competitive 1-Butyl-2,3-Dimethylimidazolium Chloride prices that fit your budget—flexible terms and customized quotes for every order.
For samples, pricing, or more information, please call us at +8615371019725 or mail to admin@sinochem-nanjing.com.
We will respond to you as soon as possible.
Tel: +8615371019725
Email: admin@sinochem-nanjing.com
Flexible payment, competitive price, premium service - Inquire now!
1-Butyl-2,3-dimethylimidazolium chloride has become a familiar part of our workbench after years of hands-on experience with ionic liquids. Its chemical architecture stands out. You can recognize the imidazolium ring structure by the way it holds both alkyl and methyl groups, the butyl replacing a hydrogen at the first position, and two methyls at the second and third. The chloride anion partners cleanly, forming an ionic liquid that melts at much lower temperatures than simple salts or conventional solvents. Our output focuses on producing the crystal-clear, high-purity (>99%) form, closely controlling residual moisture through vacuum drying and nitrogen protection from synthesis to packaging.
Colleagues in R&D noticed early on the unique behaviors this compound brings to the processes that touch it. We’ve watched the change in solubility, conductivity, and thermal stability when compared side-by-side with traditional imidazolium chlorides such as 1-butyl-3-methylimidazolium chloride (BMIM.Cl) or 1-ethyl-3-methylimidazolium chloride (EMIM.Cl). Our batch sheets confirm every time that swapping a methyl onto the 2-position, and then both 2 and 3, shifts the viscosity and the reactivity in subtle ways. You tend to lose the acidic hydrogen at the 2-position, which shapes catalytic activity and changes the way this cation stacks among other molecules.
No two ionic liquids behave the same. On the production line, minor formula tweaks mean more than just filling a different drum. Bringing 1-butyl-2,3-dimethylimidazolium chloride from flask to kilogram scale called for careful tuning. Crude material responds badly to air or water—chloride anions, in particular, grab moisture the instant they can. We invested in overhead gloveboxes, kept an eye on glass reactor seals, and watched person-hours tick up keeping things tight. Even vacuum filtration and shelf-drying add cost, but doing it right avoids hydrolysis or decomposition, which can affect downstream synthesis.
Cleanliness dominates here. As much as people chase after higher-yield chemical syntheses, at scale, contaminants often outweigh yield on the balance sheet. From the day we scaled up, attention to trace metals, residual starting imidazoles, and halide levels drew longer resource lists than any step in the initial literature. Analytical chemists in our lab apply ion chromatography and NMR analysis, as even trace impurities (including secondary amines or aldehydes) can affect enzyme compatibility, electrochemical cell potential, and organic reaction results.
While imidazolium core compounds such as BMIM.Cl or EMIM.Cl have drawn the lion’s share of attention for applications, the move to the dimethyl variant opened new avenues for our customers. Adding methyls to the 2 and 3 positions shields the C2 hydrogen, addressing common decomposition pathways. The 2-position hydrogen in BMIM cations has a reputation for participating in side reactions (including nucleophilic attack in certain carbonylations and C–H functionalizations), so knocking it out by methylation brings extra thermal and hydrolytic stability you can see directly in both glassware and the lab notebook.
Thermal gravimetric measurements we ran show higher decomposition temperatures for the dimethylimidazolium chloride than for standard BMIM.Cl, a feature that suits high-temperature transformations, advanced catalysis, or specific polymerizations where breakdown would taint yield or introduce unwanted coloration. Viscosity differences appear at room temperature, too. The 2,3-dimethyl system slips between molecules with less chance of forming sticky hydrogen bonds, so we report more favorable viscosities for flow setups or electrodeposition baths.
The customers who reach our technical support teams for this material span several fields, from chemical synthesis to battery development, to materials science and green chemistry initiatives. One routine use: as a solvent or cosolvent for tough-to-dissolve organics or transition metal salts. An ionic liquid with these particular substitutions does not just dissolve the material—it fosters an environment distinct from either pure organics or aqueous media. Carbene chemistry stands out as another field that gains from the added methyls; restricting the formation of reactive carbenes reduces poison risk and increases reaction selectivity.
Electrochemical device developers use the 1-butyl-2,3-dimethylimidazolium chloride as a room-temperature ionic conductor. Triaging energy storage technologies, we see a rising need for media that neither evaporate at low temperatures nor degrade under voltage. Our latest battery electrolyte collaboration showed this material retained fluidity and resistive performance well above 100°C, remaining stable under conditions where traditional BMIM variants developed undesirable breakdown products.
In biomass research and lignocellulose breakdown, this particular imidazolium salt outperforms many related structures. Deprotonation activity, lower acidity, and higher resistance to biological contamination let teams process cellulose or starch under less acidic and less oxidative conditions. One pilot production partner reported that switching to this chloride variant allowed tighter process control and cleaner enzymatic digestion than using simpler imidazolium-based liquids.
It is easy to lump all imidazolium-based ionic liquids into one category, but details matter—a truth hammered home in every process scale-up and every batch Q/A review. Swapping out the methyl groups in the 2 and 3 position, as in this variant, delivers real-world benefits for both researchers and production managers. The elimination of the C2 hydrogen matters most in any context where high chemical stability is mandatory; the methyls dramatically reduce decomposition during high-temperature catalysis and in electrochemical applications where stray acids or bases would bring down the process.
We see a difference in solubility. Early customer feedback flagged easier handling in multi-component solutions, especially in salt-heavy or metal-laden streams. In catalysis involving sensitive transition metals, the background reactivity and side product rate fell noticeably. With sensors and batteries, electrochemical windows widened—especially important in advanced supercapacitor prototypes and certain fuel cell concepts under review. By closely tracking melting and glass transition points, our research confirmed the performance gap between conventional imidazolium chlorides (like BMIM.Cl) and the dimethyl version. In real industrial setup, this has meant fewer shutdowns, better product recovery, and more consistent electroplating results.
Another difference lies in environmental profile. Ionic liquids have faced criticism for toxicity and biodegradability issues, but adjusting the structure can help. The removal of the C2 hydrogen, plus the methylated backbone, means this material resists some of the typical hydrolysis pathways seen in both environmental and waste management studies. Less byproduct formation means leaner clean-up efforts downstream, which one could notice first-hand in both laboratory water effluent and emissions reporting from centralized production.
At the scale of several hundreds of kilograms, minor variations accumulate rapidly. Sourcing high-quality butyl and methyl imidazole starting materials remains a logistical challenge, as impurities in starting reagents amplify exponentially in the final ionic liquid. We make sure our logistics partners understand this point, investing in regular audits and batch testing before acceptance. Direct feedback from customers evaluating batch-to-batch reliability hits home: academic research can tolerate variance, but most industrial systems cannot. Once a downstream system goes offline due to spurious reactivity or unexpected product color, trust in chemical sourcing drops.
During our own process optimization rounds, unexpected water pickup prompted investments in additional drying stages, including packed-bed molecular sieves and vacuum striping at final filling. Persistent trace amine formation found via NMR led to sourcing a new lot of starting imidazole last year, improving both product stability and end-user success rates within months. Questions about thermal decompositions or color stability come through most often from electroplating and battery research groups—industries least tolerant of byproduct deposition.
Several years ago, transferring techniques from lab bench to plant floor opened our eyes to hazards that literature rarely documents. Chloride anions, even in these advanced ionic environments, corrode steel at modest temperatures if left for extended periods. We replaced steel couplers with PTFE-lined transfer lines and allocated extra training for filling crews to handle inadvertent leaks. Our experience shows this chloride causes less skin irritation compared to other halides, but gloves and goggles remain standard operating gear. Proper labeling and secondary containment became routine, both to comply with internal safety protocols and to keep insurance auditors satisfied.
Fire risk drops almost out of sight for most imidazolium chlorides at room temperature, but we always plan facility upgrades with safe relative humidity limits and staged venting. Any process manager will appreciate how cleanup after spills, especially at loading bays in humid weather, complicates batch turnover and extends downtime. Staff training drills now prioritize leak detection and cleanup procedures specific to ionic liquids. Sharing these lessons learned has helped peer firms avoid the same mistakes we stumbled through at first.
Across the decade, customer interest in ionic liquids like 1-butyl-2,3-dimethylimidazolium chloride shifted sharply from academia and pilot projects toward entrenched industrial R&D. We don’t just ship bulk drums to far-off labs; we answer tough questions from teams hoping to replace conventional solvents or electrolytes in production. In biorefinery pilot plants, operators realized traditional amide or alcohol solvents carried higher regulatory burdens, and this material brought them nearer to compliance by lowering volatility and atmospheric release. Electrochemical and printing industries benefit when solvents no longer evaporate as quickly on open machines. Those days of simple hexane or THF are disappearing.
Carbon capture and green process development seek out materials that last longer, shed fewer VOCs, and resist breakdown under strong oxygen or CO2 loads. We’ve contributed material samples to teams tweaking absorption columns or running amine replacement studies. In almost every case, the dimethylimidazolium backbone gave durability under continuous use settings, while alternative cations failed or produced visible resin fouling over time.
It is easy to promise quality on a website; much harder to sustain over repeated quarterly orders. One of the earliest lessons from manufacturing this ionic liquid at industrial scale is that paperwork, records, and chain-of-custody audits matter as much as chemical analysis. Every drum goes out tagged for full traceability, with production lot data tied to storage and testing logs. Bulk logistics forced us to partner with only a handful of tanker outfits willing to seal drums and containers to our specifications. Our technical support does not wait for an issue; routine follow-ups and random sample retests catch shifts in quality that paperwork alone could not.
Supply fluctuation in precursor raw materials occasionally stress delivery times, so we stock enough intermediate to counter short-term gaps. End users building out pilot projects seem inevitably to double requests quarter-over-quarter once real-world trials prove the concept: early transparency and open communication with plant managers has prevented the miscommunications that previously dogged new product launches.
The next phase for 1-butyl-2,3-dimethylimidazolium chloride focuses on higher purity production and lower environmental impact. Our ongoing process refinement considers direct waste reduction, solvent recycling, and greener sourcing of starting materials—spurred by upcoming regulations and customer sustainability targets. Emissions monitoring in our updated facility tracks chloride and volatile organic output, while a closed-loop water system lowers both emissions and cost. Discussions with downstream users show an increasing drive for certified green production: tracking the lifecycle and safe disposal routes for spent ionic liquids takes attention from both lab and administration.
Partnering with academic labs broadened the tested range of this material. We now have feedback on utility in enzyme compatibility, scale-up for continuous-flow glassware, and unusual catalysis under both acid and base loading. Data from academic studies, returned to us through formal feedback agreements, gets filtered directly into everyday manufacturing methodologies. Safer, more predictable handling means fewer lost hours, less downstream cleaning, and more confidence at the application stage.
If one lesson becomes clear after producing and supporting 1-butyl-2,3-dimethylimidazolium chloride for years, it is that structure matters—both in the molecule and in the process delivering it. Extra methyl groups in the imidazolium core create small but measurable advantages everywhere from catalysis to environmental safety. As producers, we see first-hand how thoughtful chemical structure adaptation turns up in every downstream consequence: stability in electrochemical cells, batch-to-batch reliability, and safe handling inside a real-world factory. Our close work with end-users—through technical support, custom production, and process troubleshooting—means these strengths get translated where they matter, whether in a laboratory bench or industrial pilot plant.