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4-Chloro-6-(Trifluoromethyl)Benzimidazole

    • Product Name 4-Chloro-6-(Trifluoromethyl)Benzimidazole
    • Alias 4-Chloro-6-(trifluoromethyl)-1H-benzimidazole
    • Einecs 629-459-0
    • 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
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    Specifications

    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 & Storage
    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.
    Application of 4-Chloro-6-(Trifluoromethyl)Benzimidazole

    Applications of 4-Chloro-6-(Trifluoromethyl)Benzimidazole in Industrial Manufacturing

    As 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 Molecules

    Pharmaceutical 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

    • ICH Q7: GMP for Active Pharmaceutical Ingredients
    • EU GMP Part II
    • US FDA 21 CFR Part 210/211
    • Chinese Pharmacopoeia (ChP), Section on API starting materials

    Typical usage ratio

    • 0.12–0.25 molar equivalents per target API batch, with loading rate adjusted according to the molecular complexity and desired yield in multistep synthesis; process chemists fine-tune charge based on impurity profiling and batch scale.

    Downstream process integration

    • Integrated at the benzimidazole functionalization stage during liquid-phase or solid-phase synthesis; used partly in Buchwald-Hartwig amination and halogen-exchange steps, added directly after initial aromatic substitution.

    Final product types

    • Small-molecule kinase inhibitor APIs
    • Investigational oncology drug substances
    • Specialty heterocyclic building blocks for CDMO projects
    • Final bulk APIs post purification and crystallization

    2. Agricultural Fungicide Intermediate Production

    Global 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

    • FAO/WHO JMPS Requirements for Technical Grade Actives
    • ISO 9001:2015 Quality Management for agrochemical manufacturing
    • China GB 4839-2020 (Pesticide Quality)
    • REACH Annexes VII–X for chemical intermediates

    Typical usage ratio

    • 60–110 g per kg of batch active ingredient; formulation scientists tailor the input to optimize throughput and accommodate downstream derivatization yield requirements.

    Downstream process integration

    • Reacted during early-stage core ring synthesis ahead of desired side-chain introduction, frequently in acylation and condensation operations; charged into closed-system reactors under nitrogen to prevent contamination.

    Final product types

    • Technical grade benzimidazole fungicidal actives
    • Strobilurin-type fungicide actives with tailored spectra
    • Granular and suspension concentrate pesticide formulations
    • Packed bulk active intermediates for multinational crop protection brands

    3. Specialty Dye and Pigment Intermediate Manufacturing

    Selected 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

    • OEKO-TEX® Standard 100 limits on residual aromatic amines
    • Global Organic Textile Standard (GOTS), sections on synthetic raw material use
    • EU REACH SVHC and Annex XVII for dye intermediates
    • SDS documentation per GHS/CLP

    Typical usage ratio

    • 5–22 wt% relative to total pigment intermediate mass, with the proportion optimized based on target chromaticity and performance in the finished pigment; QC adjusts for batch color uniformity and solubility.

    Downstream process integration

    • Charged during nucleophilic aromatic substitution and coupling reactions for mono- and disubstituted benzimidazole pigments; typically enters the reactor after initial activation of the aromatic core and prior to azo or condensation step.

    Final product types

    • Trifluoromethyl-substituted textile dyes
    • Fastness-optimized colorants for polymer fibers
    • High-stability pigments for automotive coatings
    • Colorant dispersions for electronic and packaging inks

    4. Electronic Material Precursor for OLED Device Layers

    Manufacturers 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

    • RoHS 2011/65/EU restrictions on hazardous substances
    • IEC 61249-2-21 halogenated compound restrictions
    • ISO 14001:2015 Environmental Management (disposal limits)
    • SEMATECH Guidelines for organic semiconductor purity

    Typical usage ratio

    • 0.8–2.5 mol% relative to overall charge of organic layer intermediates, with precise metering to avoid cross-contamination and tune electronic properties; scale-up chemists adapt proportion in pilot and commercial batches.

    Downstream process integration

    • Fed into the organic synthetic route during early-stage cyclization and electrophilic functionalization for construction of advanced benzimidazole frameworks; subsequent purification ensures suitability for vapor deposition or solution processing.

    Final product types

    • Precursor molecules for OLED emitter and transport layers
    • Small-molecule hole-blocking materials for display assemblies
    • Custom OLED intermediates for display R&D programs
    • Pilot-scale samples for device lifetime and brightness testing

    5. Intermediate for Veterinary Drug Synthesis

    Veterinary 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

    • VICH GLs for veterinary medicine manufacturing
    • USP Chapter 1079: Good Storage/Distribution Practices
    • EU Regulation 2019/6 (Veterinary Medicinal Products)
    • GMP for Veterinary Drugs GB/T 16778-2017 (China)

    Typical usage ratio

    • 0.13–0.27 molar equivalents per target compound, with adjustment based on final dosage form intended and impurity acceptance criteria per pharmacopoeia monographs.

    Downstream process integration

    • Added as a functional block during molecular assembly of benzimidazole-based structures, for example, introduced following the ring closure phase via halogenation, and carried through to formulation and salt formation steps.

    Final product types

    • Veterinary antiparasitic actives
    • Benzimidazole-based animal health APIs
    • Finished dosage veterinary pharmaceutical products
    • Premix and oral suspension veterinary drugs
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    Certification & Compliance
    More Introduction

    Introducing 4-Chloro-6-(Trifluoromethyl)Benzimidazole: Manufacturer’s Insights

    Setting the Standard in Benzimidazole Chemistry

    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.

    Why This Chemical Draws Industry Attention

    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.

    Comparing to Other Benzimidazole Derivatives

    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.

    Applications Driving Real-World Value

    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.

    Production and Quality Control from the Manufacturer’s View

    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.

    Safety, Handling, and Traceability

    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.

    Sustainability, Compliance, and Global Reach

    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.

    Solutions for Common Industry Challenges

    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.

    Value in Direct Manufacturer Relationships

    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.

    What Makes 4-Chloro-6-(Trifluoromethyl)Benzimidazole Stand Apart

    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.

    Continuous Improvement: The Manufacturer’s Ongoing Story

    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.

    Closing Manufacturer Reflections

    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.