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HS Code |
712370 |
| Product Name | 4-Chloro-6-(Trifluoromethyl)Benzimidazole |
| Cas Number | 103877-64-1 |
| Molecular Formula | C8H4ClF3N2 |
| Molecular Weight | 220.58 |
| Appearance | White to off-white solid |
| Melting Point | 105-109 °C |
| Solubility | Slightly soluble in organic solvents (e.g., DMSO, DMF) |
| Purity | Typically ≥98% |
| Synonyms | 4-Chloro-6-(trifluoromethyl)-1H-benzimidazole |
| Smiles | C1=CC2=C(C(=C1Cl)C(F)(F)F)N=CN2 |
| Storage Conditions | Store at 2-8°C, keep container tightly closed |
As an accredited 4-Chloro-6-(Trifluoromethyl)Benzimidazole factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | A 25g amber glass bottle with a white screw cap, featuring hazard labels, product name, and batch information printed on the label. |
| Shipping | 4-Chloro-6-(Trifluoromethyl)Benzimidazole is shipped in tightly sealed containers to prevent moisture and contamination. It is transported as a hazardous chemical, requiring appropriate labeling and documentation. Packages are cushioned and handled with care, complying with local and international regulations to ensure safety during transit. Store upright, away from heat and incompatible substances. |
| Storage | Store 4-Chloro-6-(trifluoromethyl)benzimidazole in a tightly sealed container, in a cool, dry, and well-ventilated area. Keep away from sources of ignition, incompatible substances (such as strong oxidizers and acids), and direct sunlight. Ensure storage location is equipped with spill containment. Always label containers clearly and follow appropriate chemical hygiene and safety protocols. Avoid prolonged exposure to air and moisture. |
Applications of 4-Chloro-6-(Trifluoromethyl)Benzimidazole in Industrial ManufacturingAs a direct manufacturer of high-purity 4-Chloro-6-(Trifluoromethyl)Benzimidazole, we support advanced chemical synthesis across major industrial value chains. The following downstream sectors routinely integrate this key intermediate into their large-scale formulation and process chemistry. We ensure traceability, batch consistency, and documentation to meet regulatory, process, and customer end-use requirements. 1. Active Pharmaceutical Ingredient (API) Synthesis for Oncology MoleculesPharmaceutical manufacturers employ this compound as a core heterocyclic scaffold in the synthesis route of novel oncology APIs, especially as a functionalized benzimidazole moiety for kinase inhibitor programs. Researchers value its contribution to target selectivity via the chloro and trifluoromethyl functionalization, impacting medicinal chemistry routes. The intermediate is charged during early-stage molecule assembly and subsequent ring modifications, enabling the downstream steps in both NCE and generic molecule production. Industry compliance standards
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2. Agricultural Fungicide Intermediate ProductionGlobal agrochemical producers utilize this material within the synthesis of strobilurin and benzimidazole-class fungicides. The compound serves as a site-specific precursor for targeted ring construction, affecting antifungal activity. It features in the coupling and cyclization steps during active ingredient formation, where the electron-withdrawing trifluoromethyl group optimizes target interaction and field stability. Industry compliance standards
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3. Specialty Dye and Pigment Intermediate ManufacturingSelected specialty dye manufacturers incorporate this benzimidazole derivative in the synthesis of fluorinated pigments for fiber, plastic, and industrial coatings where both color performance and chemical durability are critical. Its structural features contribute to the creation of chromophores with controlled lightfastness, solvent resistance, and stability under processing conditions such as high temperature and UV exposure. Industry compliance standards
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4. Electronic Material Precursor for OLED Device LayersManufacturers of organic electronic materials apply this compound as a precursor in hole-transport and electron-blocking layer materials for OLED and advanced display production. The presence of both chloro and trifluoromethyl groups enables synthesis of intermediates with controlled ionization potential, beneficial for device efficiency and operational longevity. Used in a high-purity grade, it supports critical performance in downstream thin film deposition processes. Industry compliance standards
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5. Intermediate for Veterinary Drug SynthesisVeterinary pharmaceutical companies use this material to construct specialist heterocyclic frameworks for antiparasitic and broad-spectrum antibacterial medications in animal health. The chloro-trifluoromethyl benzimidazole structure modifies biological activity and pharmacokinetic behavior. It is introduced at a defined early or mid-synthesis stage depending on the animal drug target profile, with purity and traceability monitored batch by batch. Industry compliance standards
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From our years on the production floor, 4-Chloro-6-(Trifluoromethyl)Benzimidazole has grown into a specialty molecule favored by professionals in pharmaceuticals, agrochemical synthesis, and advanced research labs. The compound, recognized by its CAS number 393-96-4, owes its popularity to the tough blend of a chloro group married with a trifluoromethyl ring at the benzimidazole core. That combination doesn’t just expand its reactivity options. It’s a platform for molecular design that only a handful of other aromatic intermediates provide.
We have seen the adoption curve sharpen in step with the demand for selective bioactive scaffolds. Chemists in both the drug discovery and crop protection domains report the same benefit: the molecular backbone gives strong electron-withdrawing action, which influences binding affinity and metabolic profiles. From our reactors, purity sits at 98% or above, GC-verified every batch, and we keep residual chloride, moisture, and trace solvents tightly controlled. Those who work with process reliability know this isn't just about numbers; it defines downstream yield and consistency.
Handling this benzimidazole derivative gives a distinct advantage in multi-step syntheses. The single-site chlorination at position 4 offers a manageable anchor for nucleophilic substitution or Suzuki coupling, while the trifluoromethyl at position 6 alters physicochemical properties, often improving the biological half-life and solubility profile of derivative compounds. In many research and production campaigns, the alternative—using an unsubstituted benzimidazole or one with a nitro group—leads to longer protection-deprotection sequences, increased by-product formation, or less tractable scaling due to side reactions. This specialty compound shaves hours off campaigns by simplifying those steps.
We’ve put our production lots up against 4-nitro, 4-bromo, 5-chloro, and even the plain benzimidazole core in kilo-scale trials. Teams report fewer issues with hydrolytic degradation when they run chlorinated, trifluoromethylated intermediates at moderate pH. The electron-withdrawing trigeminal at the 6-position stabilizes the parent scaffold, reducing side reactions, especially under oxidative or acidic processing. Yields stay above 90% for key alkylation and acylation steps—rare for more reactive, less hindered analogues.
Some chemists ask about the environmental burden of a trifluoromethyl group. We address this directly on the manufacturing line. By maintaining closed-loop recovery of fluorinated solvents and using controlled atmospheric abatement, we meet regulatory limits without offshoring or diluting waste streams. From our corner of the industry, real environmental stewardship comes from continuous upgrades to abatement, not shifting the problem elsewhere.
Chemistry teams rely on 4-Chloro-6-(Trifluoromethyl)Benzimidazole to lay down heterocyclic frameworks seen in anti-infectives, oncology candidates, and proprietary herbicides. For those synthesizing kinase inhibitors, the combination of substitution pattern and backbone rigidity supports selective ATP binding, while crop science teams choose it for constructing fungicides aimed at hard-to-kill threatening pathogens.
In a typical pharma R&D setting, bench chemists run direct N-arylation or condensation with aldehydes without labor-intensive purification. The structure resists unwanted polymerization thanks to its electronic makeup. On scale-up, our experience shows this means less column chromatography, less solvent, and less workforce spent troubleshooting or chasing contaminants.
On the agrochemical side, similar benefits surface. The thermal stability of finished compounds increases, and the shelf life of products prepared from this intermediate often exceeds standard requirements, translating to more predictable performance in storage and eventual application in the field.
Working in chemical manufacturing, we know that a strong product isn’t just about a robust structure but how each batch lines up, week after week. We use stainless steel reactors lined for halogenated organics, running at carefully tuned pressure and temperature. Operators follow protocols to keep impurity profiles controlled—no random batch-to-batch excursions, no upstream guesswork. Each drum or bottle comes with detailed certificates that reflect more than spot checks. They’re based on systematic, statistical process control.
Analytical tests tie back to validated methods: GC, NMR, and LC–MS. It sounds technical, but to us, that’s the backbone of trust with end-users. As a manufacturer, we’ve learned that reliability isn’t built overnight; it’s ground out over years, through equipment upgrades, tighter process windows, and focusing on in-house staff who understand troubleshooting—not just machines following SOPs.
We’ve worked through plenty of process hazards in halogenated and fluorinated aromatic production. Chlorinated benzimidazoles demand precise temperature control, controlled atmosphere, and vigilant personal protection for bulk operators. Down the line, we label and trace every shipment. There’s no confusion or risks of mixing up intermediates for synthesis. Because compliance has only grown tighter, batch traceability goes beyond meeting local laws. It’s a commitment to downstream safety, for workers blending it into active pharma or pesticide ingredients.
Years in the business have taught us that a safe process builds from the right training, clear documentation, and an open line between plant floor and QC office. We’ve seen the cost of doing otherwise: missed specs, recalls, or worse—uncontrolled reactions that could have been prevented with tighter process discipline. For facilities looking to scale up, we’re happy to share our journey upgrading containment, from dust-extraction hoods on the milling lines to volatile-organic emission scrubbers handling the gas phase streams.
In the last decade, more customers ask about the sustainability of our processes. What happens to the waste? How do we keep emissions down? Nobody wants to be left holding the cleanup bill. Our team invests in on-site incineration for fluorinated and chlorinated waste as well as energy recovery from exothermic steps. The result is tangible—for every ton of product, fewer kilograms go to landfill, and recovered solvent circulates back into the plant systems. Auditors can verify these numbers; they aren’t just claims. These investments also protect us from regulatory shocks and changing standards, whether the product ships to North America, Europe, or Asia.
Another trend we see is a focus on supply chain transparency. Customers expect full disclosure of starting material origins, chain of custody, and documentation to back up claims. We support this by maintaining documentation for key raw materials and ensuring a tangible audit trail from procurement to finished product delivery. Frequent inspections from both within and outside the organization keep standards in real-time focus, never as an afterthought.
We know perfection isn’t possible, but the right process heads off most common headaches. By controlling the chlorination stage with close feedback loops and fail-safes for exotherms, our batches avoid the side-products that haunt less managed runs. Years ago, before these controls, we saw real costs from off-spec lots: wasted energy, wasted raw materials, and sometimes a frustrated customer on the other end of the supply chain.
On the technical side, end-users sometimes wrestle with solubility in nonpolar solvents. Based on repeat process experience, we recommend working at slightly elevated temperatures and considering solvent swaps post-reaction. For end-users seeing crystalline precipitates, small tweaks to solvent ratios or order of reagent addition can solve it—tips we’ve improved after years running developmental pilot reactors before going full-scale.
Another challenge comes with scale-up. Weird things happen when a reaction leaves the flask and enters the ton-scale reactor. Exotherms run hotter, mixing behaves differently, and old recipes break down. Our team runs simulations and pilot-lot adjustments, catching the quirks early. Sharing that know-how keeps clients from expensive mistakes, and, as manufacturers, we view that as part of our relationship—not an upsell but a professional obligation.
Buying direct changes the equation. Open dialogue between the manufacturing lab and the end-user’s technical team produces cleaner, more predictable outcomes. Supporting documentation reflects the actual plant, not guesses from an overseas distributor. We share experience in real-time: feedback from pilot lots, shipment timelines, seasonal trends affecting upstream availability, and collaborative troubleshooting when syntheses don’t behave as planned in the field or lab.
From the manufacturing side, seeing end-use cases—successful or challenging—feeds our next round of process improvements, tighter process window settings, or equipment upgrades. It’s a cycle that tightens product quality not through marketing promises but boots-on-the-floor experience, direct communication, and accountability.
Over the years, many molecules have cycled through our reactors, but few match the versatility and impact of this benzimidazole derivative. The specific positions of the chloro and trifluoromethyl groups create not just reaction handles, but avenues for innovation in targets that demand both electronic fine-tuning and metabolic resilience. The choice isn’t abstract for us—it’s reflected in improved cycle times for clients, reduced troubleshooting, and a landscape of satisfied technical teams who can predict how the compound behaves under real process conditions.
We see the differences in yield, in purity, and in long-term storage stability. For the sort of high-value, knowledge-intensive projects centered around both new chemical entities and recognizable legacy actives, this intermediate cuts extraneous steps and points users towards a streamlined process traceable from raw material barrels to the final purified compound ready for downstream work.
Manufacturing brings a never-ending flow of new expectations. We’re seeing increased scrutiny from regulators, commitment to cleaner manufacturing, and a steady drumbeat of technical demands from global customers. The latest analytical tools come into play not just to track purity, but to assure absence of potentially mutagenic impurities, halogenated byproducts, or residual solvents at levels unattainable a decade ago.
We take this as a challenge, not a burden. Our manufacturing team invests in continuous operator training, digital batch record systems, and cross-team communication. When a new impurity shows up or a process shift is needed, solutions don’t get buried in red tape—they move from operator report up to engineering, through process, and into verified, documented change.
It makes a difference in the field. Projects build on reliable groundwork, which means innovation doesn’t get stuck on revisiting yesterday’s mistakes. Our partnerships with pharmaceutical and agrochemical researchers aren’t static. They evolve each time a new product candidate needs a stricter impurity profile, greener pathway, or the latest approach to complex molecular design.
Decades of experience with halogenated aromatic production tell us that specialty chemicals like 4-Chloro-6-(Trifluoromethyl)Benzimidazole set the tone for what’s possible in modern synthesis. It stands out to technical teams who weigh each step, who remember every failed reaction, and who know how a single bottleneck can capsize budgets and timelines. The compound’s unique features—selective reactivity, strong performance in challenging reaction conditions, and a robust, scalable process—have made it a tool with staying power in dynamic industries.
Talking about it from the production side, it’s the result of steady refinement, hands-on troubleshooting, and openness to new ideas—qualities that underpin the progress of new drugs and advanced agricultural technologies. We don’t market dreams; we deliver batches shaped by expertise and built for teams who care just as much about moving the science forward.