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HS Code |
322437 |
| Product Name | 4,5-Dichloroimidazole |
| Chemical Formula | C3H2Cl2N2 |
| Molecular Weight | 136.97 g/mol |
| Cas Number | 29341-60-6 |
| Appearance | White to off-white solid |
| Melting Point | 118-121°C |
| Solubility | Soluble in polar solvents such as DMSO and DMF |
| Purity | Typically ≥98% |
| Storage Conditions | Store in a cool, dry place, tightly closed |
| Smiles | C1=NC(=CN1Cl)Cl |
As an accredited 4,5-Dichloroimidazole factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 4,5-Dichloroimidazole, 25g, is supplied in a sealed amber glass bottle with a tamper-evident cap and printed hazard labels. |
| Shipping | **Shipping Description for 4,5-Dichloroimidazole:** This chemical is shipped in tightly sealed containers, protected from moisture and incompatible materials. It should be labeled according to applicable hazardous material regulations. Packages are cushioned to prevent breakage and stored in a cool, dry place during transit. Ensure compliance with local and international transport safety guidelines. |
| Storage | 4,5-Dichloroimidazole should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from incompatible substances such as strong oxidizing agents. Protect from moisture and direct sunlight. Properly label the storage area and ensure it is designated for hazardous chemicals. Use secondary containment to prevent spills and limit access to trained personnel only. |
Applications of 4,5-Dichloroimidazole in Industrial Manufacturing4,5-Dichloroimidazole is a specialized intermediate essential to the synthesis of a select range of value-added compounds. Our in-house expertise ensures tightly controlled specifications to meet the requirements of established downstream sectors. The following application scenarios demonstrate how industry leaders integrate our material into their operations under exacting quality and compliance mandates. 1. Active Pharmaceutical Ingredient (API) Synthesis for Antifungal AgentsPharmaceutical manufacturers rely on 4,5-dichloroimidazole as a key heterocyclic building block in multi-step syntheses of azole-based antifungal drugs. This material undergoes controlled condensation reactions to introduce chlorinated imidazole moieties crucial for bioactivity. Its defined purity levels and reactivity profile support regulatory submission and batch traceability, with dosing ratio adjustments tied to specific API target pathways and process yields. Industry compliance standards
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2. Agricultural Fungicide Intermediate ManufacturingAgrochemical companies use 4,5-dichloroimidazole as a core intermediate to introduce functionalized imidazole rings into next-generation triazole and strobilurin fungicides. Precision chlorination and purity are critical to minimize formation of side products in oxidative coupling stages. Downstream formulation teams adjust input ratios to optimize conversion rates unique to each branded molecule. Industry compliance standards
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3. Speciality Polymer and Resin Additive SynthesisSelect specialty polymer manufacturers utilize 4,5-dichloroimidazole to build imidazole-functionalized monomers and pre-polymers for high-performance resin systems. Control over chlorine substitution directly impacts downstream crosslink density and thermal resistance. Batch dosing relies on target monomer-to-initiator ratios established by resin application demands, from electronics encapsulation to adhesives. Industry compliance standards
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4. Electrolyte Additive for High-Performance Lithium-Ion BatteriesBattery material producers integrate 4,5-dichloroimidazole derivatives into advanced electrolyte additive cocktails to enhance electrolyte stability and improve electrode passivation in Li-ion cells. Strict impurity controls reduce risks of side reactions impacting battery cycle life. Process engineers adjust inclusion rates based on electrolyte blend composition, operational voltage windows, and target SEI layer characteristics. Industry compliance standards
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From behind the scenes of chemical production, years of hands-on synthesis and direct problem-solving offer a closer look at how real work gets done. In our plant, 4,5-Dichloroimidazole has earned its place as a foundation-block for several high-performance intermediates, especially for those producers who require tight process controls or sustainable feedstocks. Compared to many specialty heterocycles, this molecule offers a unique interplay of reactivity and selectivity. Over time, we have learned the quirks and handling priorities needed for our facility.
We produce 4,5-Dichloroimidazole to a highly-purified standard, geared for use by research groups and manufacturers involved in complex synthesis. Our recent batches regularly reach a purity above 98%, verified by in-house HPLC and GC-MS. The product usually appears as a crystalline solid, off-white to faint yellow. A melting point in the 110–115°C range signals proper formation, but the real checks happen during downstream synthesis, where impurities or off-batches can throw off reaction consistency.
Moisture content remains critical, especially for those using it for scale-up. Even trace water or acidic residues can skew reactivity. Regular Karl Fischer titration routines confirm that our product meets sub-0.3% water content on dispatch days. Particle size distribution stays within the demanded mesh ranges for our customers' processes, supporting straightforward handling in most laboratory and production-scale reactors.
From a manufacturer’s perspective, what distinguishes this molecule sits beyond the specification sheet. Being a fully chlorinated imidazole means two things: enhanced chemical resilience and strategic points for further substitution. Chemists tasked with multi-step synthesis—especially those in pharmaceuticals and agricultural research—want intermediates they can tune further. The 4,5-dichloro positions on the imidazole ring allow for nucleophilic aromatic substitution, making downstream modifications practical and efficient without tedious protection/deprotection cycles commonly needed for less reactive halogenated analogs.
Other substituted imidazoles, such as monohalogenated or nitro variants, don’t behave in quite the same way. We’ve watched research teams lose yield or struggle with reproducibility when using alternatives. With 4,5-Dichloroimidazole, the double-chloro motif translates into greater control over regioselectivity and reduced by-product formation in some of the most demanding transformations. In certain syntheses, side-chain patterning occurs more cleanly and with better atom economy than with the widely available 2-chloro or 4-nitro imidazole relatives.
Feedback loops with specialty pharmaceutical groups and custom fine-chemical projects inform much of our plant’s process development. For those pursuing purine or imidazopyridine structures, this heterocycle often figures as a pivotal intermediate, with direct implications for medicinal chemistry and active ingredient design. The material finds use in exploratory oncology compounds, advanced antiviral candidates, and occasionally specialty crop-protection actives or ligands in catalysis.
Bench chemists, including many who have visited our plant, highlight how 4,5-Dichloroimidazole offers a productive balance between reactivity and stability. Its tendency to remain intact under moderately harsh conditions gives end users the flexibility to run multi-step sequences without excessive decomposition or chlorination drift. This trait also helps R&D teams keep analytical workloads down, reducing the number of checks needed as reactions progress.
We have also taken part in several collaborative projects where this material essentially enabled a new route—making certain synthetic targets feasible that otherwise required lengthy alternatives or less scalable procedures. As a direct precursor, it cuts steps and costs for certain key heterocycles. Its popularity with medicinal chemists reflects this, as many modified imidazoles end up as kinase inhibitors, antifungals, or imaging agents that never reach the market but drive discovery forward.
Producing chlorinated imidazoles always comes with obstacles, particularly with respect to chlorination selectivity and the removal of minor isomers. Considerable time has been spent refining our process so only 4,5-dichloro isomers emerge at useful scale. A batch that falls out of spec typically shows up first in downstream coupling or substitution, where yield dips and HPLC reveals unwanted tar. Early on, we dealt with plenty of these frustrations.
Through iterative pilot runs, consistent feedstock evaluation, and in-situ testing, our team improved the selectivity of the halogenation step. Each adjustment requires long hours with both analytical chemists and operators. Getting the right balance between reaction temperature, solvent choice, and agitation speed can spell the difference between a material that customers trust and one that causes more troubleshooting than it’s worth.
We never discount the human element. No process comes together in a vacuum. Operators rely on physical signs as much as meters: the hue and crystallization behavior, the way vapor carries in process lines, the way certain impurities behave under column-purification. Some of our best troubleshooting stems from careful observation and experience passed from colleagues over thousands of runs.
No real-world producer ignores the environmental and occupational issues surrounding halogenated intermediates. The way our chemists and operators interact with bulk 4,5-Dichloroimidazole differs from typical lab-scale routine. Standard procedures involve closed-system filtration, rigid attention to solvent recycling, and specialized PPE. Bulk handling focuses keenly on dust minimization, as fine powders present inhalation risks and cross-contamination headaches.
We've worked to reduce solvent usage and reclaim as much chlorinated waste as possible, not because of regulation alone, but because tight controls reduce cost and reduce liability. Our plant recycles chlorination solvents and works with licensed partners to recover or destroy residuals, keeping our total waste output manageable.
All staff on production lines undertake yearly chemical safety refreshers specific to this class of compound. Operations teams identify pinch points where accidental exposure or minor spills could occur, redesigning procedures when new insights surface. Gloves, goggles, and respirators remain standard—a familiar but essential barrier in day-to-day operation. Regular dialogue between health and production teams strengthens our site’s safety culture and helps catch emerging risks before incidents occur.
Shipments use robust containment for both domestic and international logistics, targeting moisture ingress and breakage in transit. Customers in tropical or maritime climates have reported issues in the past, so we’ve tuned our packaging and added real-time temperature and humidity loggers to longer haul shipments. Getting feedback direct from a customer site—whether praise or a complaint—drives improvements faster than paperwork ever can.
Years of side-by-side production and customer feedback provide sharp insights into how 4,5-Dichloroimidazole stands up to its chemical siblings. The big differences fall on reactivity, process behavior, and application scope.
Take 2-chloroimidazole as an example. It sometimes shows up in literature as a substitute, but our process teams and customers routinely encounter higher byproduct levels or stubborn purification bottlenecks. The ortho-chloro group creates a much different electronic landscape within the ring, which in turn affects everything from nucleophilicity at adjacent sites to stability under basic conditions.
4,5-Dichloroimidazole offers more controlled downstream transformations. Its clean, symmetric substitution pattern minimizes ambiguity during ring-expansion and coupling reactions. Research groups appreciate fewer complications in NMR or LC/MS data, as the unwanted isomers are kept to a minimum right from the start of the supply chain.
Differences also emerge in how these molecules handle scale-up. Some analogs require cryogenic steps, excess base, or especially careful venting protocols. Our facility tackles these obstacles through re-engineered reactor hardware and tailored workup steps, keeping bulk production both cost-effective and consistent. End-users have commented that their processes generate fewer wastes and proceed more smoothly when they receive our high-purity material over random-batch alternatives.
Nitroimidazole variants offer yet another point of comparison. Their downstream chemistries trend toward reduction-sensitive environments and may yield more oxidative side-products. 4,5-Dichloroimidazole doesn’t suffer from these quirks; most customers pursuing robust, high-yielding multi-step syntheses overwhelmingly select it when given the chance.
Pharmaceutical and research partners drive home a single theme: consistency from batch to batch. For synthetic chemists, frustrating variability shows up as late eluting HPLC peaks or mysterious TLC spots. Years ago, even minor deviations in our batch workups foiled gram-scale pilot runs, and we’ve spent many cycles homing in on repeatable purity and reproducibility.
Our internal QC practices rely equally on technology and intuition built from decades of producing halogenated heterocycles. No instrument alone signals a perfect batch—the seasoned chemists spot the tiny color shifts or texture changes that betray a future problem. Reproducibility lets our partners spend less time on purity checks and more time on innovation or scale-up, tightening timelines and cost projections.
We’ve also seen the downstream impact. Large pharma campaigns and academic groups have built entire routes around our material’s reliability. Failures are expensive, and the fewer that occur, the greater our reputation grows in a tight-knit community of technical buyers.
Our approach to 4,5-Dichloroimidazole owes much to partnership. In the early days, we fielded ongoing feedback from customers, often accommodating minor specification tweaks or shipment adjustments based on their exact needs. Those collaborations taught us how a seemingly small change in crystal habit or moisture profile left a large fingerprint on final yield or purity.
Transparency and direct dialogue count for a great deal. We field questions on analytical traces, supply raw chromatograms if requested, and track lot-level data for years after a batch ships out. Sometimes, feedback from customers prompts changes to synthesis routines or package configurations, building trust and deepening our understanding of how this material behaves across different applications.
The flow of information doesn’t stop at the loading dock. Networking with academic labs or research consortia means that we hear about upcoming application needs—be it new derivatizations, unusual purifications, or research on large-scale applications. We’re able to anticipate shifts in the market and prepare for new testing or regulatory oversight before crises occur.
Growth in specialty pharmaceuticals and advanced agrochemicals continues to drive sharp demand. We’ve noticed increasing calls for greener chemistry and supply chain resilience, giving us clear signals to innovate process design and minimize overall environmental impact.
One emerging challenge centers on regional regulation and logistical complexity. With border controls and environmental governance tightening worldwide, the strategy increasingly hinges on traceability and adaptability. Companies relying on our intermediates want assurance that what they receive conforms not just to technical specification but to a transparent supply chain.
The call for greener production will not fade. Our facility looks at better solvent recovery and lower waste approaches. Process engineers test catalysts and alternate chlorinating agents, seeking reductions in byproduct load and emissions. These aren’t trivial changes. After years of continuous improvement, plant teams measure even minor resource savings and pass the benefit along to customers who track both cost and sustainability metrics.
Automation and improved data logging create new data sets for process control and root-cause analysis. Good manufacturing practice means not just running recipes, but looking for every way to anticipate risks and catch emerging quality issues before they hit a customer’s plant. Our future rests on both agility and a deep well of experience built over thousands of production runs.
Every batch of 4,5-Dichloroimidazole carries a history of practical know-how, experimental data, and shared insight. Our chemists’ and operators’ successes and failures shape every improvement to process and quality. Customers recognize and value that reliability because it translates into real productivity and peace of mind.
We stand at the intersection of chemical invention and industrial discipline. Through careful manufacturing, robust quality assurance, and direct engagement with the scientific community, we’ve made 4,5-Dichloroimidazole a trusted tool for advanced projects worldwide. Continuous feedback from the bench and production floor ensures that the material delivers as promised.
Our perspective, sharpened by decades in the field, keeps us focused on the core principles: safety, reproducibility, open communication, and progress—so the next innovation cycle can build on a foundation that doesn’t break under pressure.