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4-Chloro-2-Mercapto-6-(Trifluoromethyl)Benzimidazole

    • Product Name 4-Chloro-2-Mercapto-6-(Trifluoromethyl)Benzimidazole
    • Alias 4-chloro-6-(trifluoromethyl)-1H-benzimidazole-2-thiol
    • Einecs 429-480-9
    • 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
    VTB
    Specifications

    HS Code

    942423

    Chemical Name 4-Chloro-2-Mercapto-6-(Trifluoromethyl)Benzimidazole
    Molecular Formula C8H3ClF3N2S
    Molecular Weight 252.64 g/mol
    Cas Number 75706-12-6
    Appearance Off-white to light yellow powder
    Melting Point 181-185 °C
    Solubility Slightly soluble in water, soluble in organic solvents
    Storage Conditions Store in a cool, dry place, tightly closed
    Purity Typically ≥98%
    Synonyms 4-Chloro-6-(trifluoromethyl)-1H-benzimidazole-2-thiol
    Smiles C1=CC2=C(C(=C1Cl)C(F)(F)F)N=C(S2)N
    Hazard Statements May cause skin and eye irritation
    Usage Intermediate in pharmaceutical synthesis

    As an accredited 4-Chloro-2-Mercapto-6-(Trifluoromethyl)Benzimidazole factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 100g chemical is packaged in a sealed amber glass bottle with a tamper-evident cap and hazard labeling for laboratory use.
    Shipping 4-Chloro-2-Mercapto-6-(Trifluoromethyl)Benzimidazole is shipped in tightly sealed containers to prevent moisture and light exposure. It is labeled for chemical use, and handled per relevant hazardous material regulations. Shipping complies with UN, ICAO, and IATA guidelines as applicable. Appropriate documentation and safety data sheets are included with all shipments.
    Storage Store **4-Chloro-2-Mercapto-6-(Trifluoromethyl)Benzimidazole** in a cool, dry, well-ventilated area away from direct sunlight and incompatible substances such as strong oxidizers. Keep container tightly closed and clearly labeled. Handle under inert atmosphere if possible to prevent moisture exposure. Use personal protective equipment when handling, and avoid inhalation, ingestion, or skin contact. Store at recommended temperature as per manufacturer’s guidelines.
    Application of 4-Chloro-2-Mercapto-6-(Trifluoromethyl)Benzimidazole

    Applications of 4-Chloro-2-Mercapto-6-(Trifluoromethyl)Benzimidazole in Industrial Manufacturing

    4-Chloro-2-Mercapto-6-(Trifluoromethyl)Benzimidazole supports a range of specialized industrial applications due to its unique structural properties and chemical reactivity. As the original manufacturer, we supply this intermediate directly to formulation and production lines in established downstream sectors, focusing on industries with documented process integration and compliance requirements.

    1. Synthesis of Agricultural Fungicides

    Agrichemical formulators use this benzimidazole derivative as a building block in the production of advanced fungicidal active ingredients for crop protection. It provides stability and fungitoxicity essential for modern formulations targeted at resistant fungal pathogens. Its integration occurs during early synthesis, often through nucleophilic substitution and subsequent functional group modifications to deliver final actives that must comply with residue and environmental limits globally.

    Industry compliance standards

    • FAO/WHO: Specifications for Plant Protection Products
    • EPA (US): 40 CFR Part 180 - Tolerances and exemptions for pesticide residues
    • REACH (EU): Registration and safety data for intermediates
    • China: GB 2763—National Food Safety Standard—MRL of Pesticides

    Typical usage ratio

    • 5-15% as intermediate in fungicide active ingredient synthesis; adjusted according to molecular design and target efficacy.

    Downstream process integration

    • Reaction batch charging during heterocyclic core formation.
    • Further processing through alkylation or acylation steps as required by target molecule.
    • Purification by recrystallization or chromatic separation.
    • Transfer to formulation lines for final technical grade blending.

    Final product types

    • Suspension concentrate (SC) fungicides for wheat, barley, and rice protection.
    • Technical-grade crop protection actives targeting ascomycete fungi.
    • Water-dispersible granules (WG) for fruit and vegetable field application.
    • Seed treatment fungicides used in major grain markets.

    2. Dye Intermediate for Specialty Performance Dyes

    Colorant manufacturers employ this benzimidazole-based intermediate in the synthesis of lightfast dyes applied in polymer fibers and high-end industrial textiles. The unique trifluoromethyl substitution supports chromophore stability and resistance to UV degradation in severe use environments. The material enters multi-step condensation and coupling reactions, influencing both hue and durability properties.

    Industry compliance standards

    • Oeko-Tex Standard 100 for restricted substances in dyed textiles
    • ZDHC MRSL for textile chemical input safety
    • ISO 9001:2015 for colorant manufacturer quality management
    • European Regulation (EC) No 1907/2006 (REACH) with focus on dye substance registrations

    Typical usage ratio

    • 3-12% as chromogenic intermediate, fine-tuned based on target color strength and application medium (fiber, plastic, ink).

    Downstream process integration

    • Included in azo or anthraquinone dye core synthesis via direct aromatic substitution and coupling.
    • Process may involve chlorination, sulfonation, or other functional group modifications post-coupling.
    • Subsequent purification ensures product meeting spectral purity standards for industrial textile applications.
    • Final product compounded or dispersed into masterbatch or aqueous formulations.

    Final product types

    • High-performance non-fading textile dyes for workwear and sportswear fabrics.
    • Lightstable colorants in automotive plastics and fiber-reinforced resins.
    • Industrial inkjet inks for technical printing on polymer substrates.
    • Commercial powder dyes for carpet and upholstery yarns.

    3. Pharmaceutical Intermediate for Heterocyclic Drug Substances

    API manufacturers utilize this benzimidazole derivative as a core intermediate when constructing select heterocyclic pharmaceutical actives, especially those requiring both sulfur and halogen moieties for pharmacological activity. The compound’s role covers multi-step synthesis for molecules targeting therapeutic areas such as antimicrobials, antiparasitics, and anti-inflammatory agents, with strict traceability and impurity control during validation and commercial production.

    Industry compliance standards

    • ICH Q7: Good Manufacturing Practice guidance for Active Pharmaceutical Ingredients
    • USP and EP monographs where applicable for specific actives
    • 21 CFR Parts 210/211 (FDA cGMPs for finished pharmaceuticals)
    • Chinese Pharmacopoeia quality and impurity guidelines for intermediates

    Typical usage ratio

    • 8-20% in synthetic route; adjusted according to API molecular complexity and step yield.

    Downstream process integration

    • Charged at intermediate synthesis stage, often following base-catalyzed cyclization or electrophilic aromatic substitution.
    • Passed through sequential purification steps, including activated carbon and column chromatography.
    • Used in multi-step build-up toward the finished heterocyclic active ingredient structure.
    • Subjected to validated kill steps to control residual levels and ensure overall process compliance for API submission.

    Final product types

    • Heterocyclic active pharmaceutical ingredients in tablet and capsule dosage forms.
    • Bulk intermediates for veterinary pharmaceutical actives.
    • Select antiparasitic drug actives produced under DMF filing arrangements.
    • Finished bulk actives for contract API manufacturing customers in regulated markets.

    4. Corrosion Inhibitor Additive for Industrial Water Treatment

    Specialty chemical formulators integrate this benzimidazole compound in water treatment blends to provide targeted corrosion protection, especially in challenging systems operating with high chloride content and variable pH. The presence of the trifluoro and mercapto groups enables performance in protecting ferrous and non-ferrous metals, important for power plant cooling, process water recirculation, and heavy industry. Its use falls under quantitative dosing protocols with monitoring for compliance with health and environmental regulations.

    Industry compliance standards

    • ANSI/AWWA B100, B121 – Additive material criteria for water treatment
    • EU Biocidal Products Regulation (BPR, Regulation (EU) 528/2012) for use in closed-system additives
    • NSF/ANSI/CAN 60 for chemicals used in potable water treatment (if applicable)
    • ISO 14001:2015 for environmental management systems (where required)

    Typical usage ratio

    • 0.1-0.5% active content in water treatment blend, adjusted according to system throughput, corrosion rate, and monitoring feedback.

    Downstream process integration

    • Added to corrosion inhibitor concentrate at formulation or let-down stage.
    • May be co-blended with azoles, phosphonates, and nitrites as system-specific formulations demand.
    • Directly dosed into water recirculation circuits or cooling towers under monitored feed rates.
    • Subject to periodic field testing for product efficacy and regulatory compliance.

    Final product types

    • Closed-system corrosion inhibitor blends for power plants and heavy industry.
    • Blended chemicals for oil refinery heat exchanger protection.
    • Recirculating water additives in pulp and paper process systems.
    • Specialty products for use in district cooling or heating plant systems.

    5. Intermediate for Specialty Polymer Stabilizers

    Polymer additive manufacturers employ this material in the synthesis of heat and light stabilizer molecules for use in engineering plastics exposed to high-service temperatures and outdoor weathering. Its structural motifs deliver performance especially in UV absorber and anti-degrading additive types, integral to meeting durability requirements in demanding end-use markets. Integration into the additive molecule is fine-tuned at the condensation phase, enabling adjustment of reactivity and polymer compatibility.

    Industry compliance standards

    • RoHS Directive 2011/65/EU and amendments for restricted substances in electronics and plastics
    • FDA 21 CFR 177.1520 for additives in food-contact polyolefins (if applicable)
    • UL 94 flammability standards for electrical and automotive polymers
    • ISO 4892-2 for accelerated weathering test protocols (performance validation of final plastics)

    Typical usage ratio

    • 2-7% in specialty light/heat stabilizer compound production, varied according to targeted additive loading and host polymer characteristics.

    Downstream process integration

    • Engaged at the monomer modification, condensation, or cyclization steps in stabilizer synthesis.
    • Further functionalization and blending with antioxidant or HALS systems may follow, depending on formulation targets.
    • Stabilizer dispersed directly into masterbatch for downstream compounding.
    • QC assessment prior to finished-goods shipment to plastic processors.

    Final product types

    • UV absorber additives for automotive and construction plastics.
    • High-temperature polymer stabilizers used in appliance housings and high-voltage insulation.
    • Color-retaining additives in exterior electrical enclosures and outdoor furniture.
    • Custom additive packages for film extrusion and fiber spinning processes.
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    Certification & Compliance
    More Introduction

    4-Chloro-2-Mercapto-6-(Trifluoromethyl)Benzimidazole: Experience from the Production Floor

    What We’ve Learned Manufacturing 4-Chloro-2-Mercapto-6-(Trifluoromethyl)Benzimidazole

    Many years on the factory floor don’t get replaced by brochures or market surveys. We rely on what we’ve seen in practice—how compounds behave, what sparks the interest of synthetic chemists, and, most importantly, what stands up to real-world demand. Working with 4-Chloro-2-Mercapto-6-(Trifluoromethyl)Benzimidazole is a clear example. This compound, with its strong chemical backbone and unique electron-withdrawing trifluoromethyl group, rose up due to persistent requests from researchers seeking niche substitutions in their benzimidazole scaffolds. Its emergence in our product line didn’t follow a trend; it came from repeated asks for a solution not just stable on a shelf but consistently reactive where it matters.

    The model we provide most commonly reflects what the labs prefer: material with a purity not less than 98 percent, tested batch to batch by trusted hands using both HPLC and NMR. Specifications such as melting range, moisture content, and residual solvents are controlled tightly, not just for a certificate but from pragmatism—chemists cannot afford guessing games when optimizing their syntheses. Our typical production scale meets kilogram requests yet can ramp up or pare down depending on the project or pilot-study needs.

    Why This Structure Earns Its Spot in the Toolbox

    Any chemist watching the evolution of heterocyclic development will spot why this benzimidazole variant draws attention. The presence of a chloro group and a mercapto function—or thiol—opens opportunities for targeted transformations. We’ve seen entire synthetic routes hinge on the selective reactivity of the mercapto group, especially for custom intermediates going into fungicide and pharmaceutical discovery pipelines. The trifluoromethyl group, on the other hand, imparts a boost to both metabolic stability and lipophilicity. Years ago, adding a CF3 group was an expensive gamble, but that situation changed as the demand for bioactive molecule libraries grew. You see it now in patents linked to kinase inhibitors, anti-infectives, and crop protection leads.

    Our customers don’t just ask for the molecule by IUPAC name—they cite their need for a high-yielding, reliable thiol source that also brings in the added electronic effects from the CF3 group and the ortho chloro substitution. This means not every benzimidazole, mercapto-derivative, or trifluoromethylated scaffold performs the same way. We handle the material knowing the subtle differences in solubility, reactivity, and downstream compatibility from years spent seeing where other compounds give out.

    Production Lessons: Handling, Scaling, and Purity

    During scale-up production, handling a compound bearing both chloro and mercapto groups presents a set of challenges. Our teams learned early to monitor for trace oxygen and avoid extended exposure, since even minute oxidation can blunt downstream reactivity. Outgassing steps have been optimized, and many of our reactor operators now anticipate both the smell and volatility of the mercapto component when they open reaction vessels. We adjusted production schedules over the years to account for these stages, and our quality assurance staff became fluent in tracking minor variants or degradants, ensuring they never slip into the main batch.

    Where analytical theory meets reality is in identifying and profiling side products. Early attempts at making this compound in open vessels led to unwanted sulfoxide and disulfide impurities—good learning points, reminders that benchtop procedures don’t always translate directly to ton-scale plants. We put in closed-process isolation steps and built in real-time monitoring, which paid off in batch consistency. Practically, this means we see fewer complaints about lots drifting outside specification; reputation matters just as much as paperwork here.

    Working with seasoned partners in analytical chemistry, we developed matching verification protocols suitable for both regulatory and innovative research contexts. Our QA doesn’t just tick boxes; they dip into samples, run tests in triplicate, and double-check reference spectra against independently-sourced analytical standards. Our warehouse only moves out what’s cleared final release—another habit learned from earlier mistakes across many products, not just benzimidazoles.

    Applications Seen in the World Beyond the Lab

    Every time a customer describes their end-use, it adds to our internal database of practical knowledge. Most new demand comes from intermediates for pharmaceuticals, crop protection actives, and specialty materials. The thiol group, especially, stands out in preparing further derivatives via alkylation or acylation, helping build sulfur-bridged, fluorinated heterocycles. Over the past decade, as fluorine chemistry moved from specialist domains to broader agrochemical and medicinal development, this molecule found itself in new utility roles, not just as a final target but as a pivot for constructing more complex compounds.

    Some ask us how this particular compound differs from others in our line. Beyond the obvious functional group arrangement, reactivity sets it apart: the trifluoromethyl group, which usually resists most nucleophilic attack, still stabilizes the molecule’s core. We’ve watched the differences firsthand—yields after coupling or S-alkylation reactions climb in step with batch-to-batch purity, but so does the selectivity in constructing chiral centers. Other benzimidazole derivatives lacking the CF3 or mercapto group can’t always match this performance, especially in iterative or automated synthesis runs. Even in decomposition studies, we’ve recorded the CF3 variant’s improved shelf lifespan against moisture and heat.

    What Goes Into Consistent Batches and Real-World Supply Chains

    We often receive queries from process chemists or purchasing managers who recall the unpredictability of spot buying. They’ve handled lots of variable quality, visible color shifts, and product with residues that complicate purification. That’s what we address daily. Every cycle, our operators run samples through both in-process and release analytics. Deviations, even by less than a percent, prompt a double-check and, when needed, a controlled remix of the batch. These habits didn’t appear overnight; they emerged from years of unscheduled plant downtimes, customer phone calls about performance drops, and traces of impurity showing up in unexpected places.

    Logistics teams, too, play a part. Winter shipments require different packing protocols, especially if condensation is at risk. High summer humidity—common in this part of the world—compelled us to design layered moisture barriers. It’s these operational details, more than the chemistry, that decide whether research timelines get met. We keep extra time in our schedules for follow-up testing and never push out a shipment that’s not up to code, whether the destination is a small outlet lab or a multi-site research park.

    After-sale feedback forms a constant loop. Chemists and engineers often provide direct reports about any crystalline changes, unusual odors, or issues in solvent compatibility. Each comment feeds our continuous improvement plans and, unlike distant traders, we get those insights first-hand—enabling us to tweak not just one lot, but the next production run.

    Direct Comparisons: 4-Chloro-2-Mercapto-6-(Trifluoromethyl)Benzimidazole and Its Relatives

    On paper, similar compounds can look interchangeable. In synthesis and process work, differences emerge rapidly. Some customers use a 2-mercapto benzimidazole without the trifluoromethyl group and find they must adjust solvent ratios, reaction times, and post-processing methods. Others have switched from benzimidazole with ortho-fluoro or ortho-bromo groups, only to notice side products form under their usual conditions. Years of comparative runs in our own pilot lab, and reports from clients, have demonstrated the unique balance this compound achieves—reactive enough to build upon, stable enough for transit and storage, and with a melting range fitting downstream isolation needs.

    Where some chemicals offer cost savings at scale but trade away reliability, we’ve kept metrics on how small changes in the molecular structure impact yield, reproducibility, and downstream safety tests. The trifluoromethyl group, especially, performs as expected in electron-rich substitution environments, cutting down on discoloration and improving overall product performance. By contrast, analogues with only a chlorine or mercapto function at other positions show varied rates of hydrolysis or fail regulatory screens for impurities. We don’t just compile these points for technical datasheets; we track them so our own processes evolve along with the demands of the market.

    In feedback sessions, some customers detail differences in extraction protocols or column chromatography when switching between the 4-chloro-2-mercapto-6-trifluoromethyl benzimidazole and other functionalized benzimidazoles. Rather than producing generic guidance, we offer batch-specific insight, because practice shows that theoretical yield doesn’t always match experience. Having worked side by side with chemists troubleshooting these variations, we understand the frustrations caused by seemingly minor structural shifts, and we proactively address those points in each order cycle.

    What Responsible Manufacturing Looks Like

    As global regulatory scrutiny tightens, we operate under established local and international guidelines regarding purity, documentation, and traceability. Our processes meet current requirements for both pharmaceutical and non-pharmaceutical grades, relying on regular audits and robust digital records. We believe transparency strengthens trust. Details on impurity profiles, trace element content, and sourcing remain available to all end users, not just regulatory agencies. Years working directly with innovators facing regulatory hurdles mean we prepare support statements, method validations, and stability data in formats that simplify submission and accelerate approvals. We keep lines open for any data requests—knowing that one-size-fits-all rarely satisfies the ever-growing compliance expectation.

    Raw materials sourcing plays a substantial role in consistent, safe production. After experiencing supply disruptions and lots affected by upstream variation, we long ago moved to a qualified vendor system, testing incoming precursors beyond the bare minimum—every acceptance relies on repeat sample analysis, never on generic supplier guarantees. Our relationships with vendors remain ongoing, subject to annual review and frequent quality benchmarking. Any major change upstream triggers internal review, new pilot-scale confirmation, and direct communication with clients likely to notice unforeseen impacts.

    Supporting Innovation Across Multiple Fields

    Most breakthroughs in pharmaceuticals, crop science, and advanced materials rest on the shoulders of dependable starting materials and intermediates. We make it our business to know, not just the immediate market for 4-chloro-2-mercapto-6-(trifluoromethyl)benzimidazole, but where researchers push into new applications. Sometimes a phone call from a small biotech uncovers a brand-new receptor target; in another case, an agricultural scientist needs a batch for an urgent field trial due to an unexpected pest outbreak. Instead of working on autopilot, we reserve production flexibility so high-priority projects move into our cycle quickly.

    We’ve seen university labs, contract R&D outfits, and multinational firms each evaluate new candidates built upon this benzimidazole scaffold. Our part is not just delivering a chemical, but adapting batch size, documentation support, and drop-shipping based on variable research timelines. With dozens of conversations every year about revised structural analogues, we stay close to the leading edge of substitution trends and corresponding performance data, giving us a feedback-driven approach no third-party intermediary can match.

    Many researchers now prioritize improved metabolism in vivo, greener syntheses, or reduced byproduct formation. Our own production adjustments—lower solvent volumes, recycling of process streams, and elimination of non-essential additives—allow us to offer material that aligns with these evolving benchmarks but still maintains the robustness required for demanding synthetic routes.

    Collaborative Solutions for Complex Challenges

    Problems rarely arrive the same way twice. Sometimes it’s a delayed shipment that demands rapid reallocation of stock across continents. Other times, it’s a formulation bottleneck revealed weeks after a delivery. We believe honest, direct feedback provides the clearest solutions. Inside our company, every member involved with 4-chloro-2-mercapto-6-(trifluoromethyl)benzimidazole has a stake in addressing both production hiccups and downstream application issues. Our technical support team includes staff cross-trained in both synthesis and plant troubleshooting. When a batch falls outside the usual physical specification, we scramble a rapid task force to diagnose, correct, and—most importantly—prevent future repeats.

    Some of the challenges our team has solved include optimizing crystallinity for selective reactivity, managing varying moisture content across seasons, and adjusting particle size for better processability in downstream blending and formulation. Our late-stage engineers have modified filtration and drying steps to balance throughput and final product properties, based on both scale-up studies and partner site feedback. Our partnership with expert logistics staff ensures the highly sensitive thiol group stays protected from oxidation until it arrives at the customer’s door, whether that’s a laboratory loading dock or an industrial formulation plant.

    Looking Forward: Building on a Foundation of Knowledge

    In the chemical manufacturing world, reputation grows from learning by doing, paying attention to every customer’s experience, and refusing the shortcut mentality. For 4-chloro-2-mercapto-6-(trifluoromethyl)benzimidazole, that means more than pushing out certified lots. Trust builds from reliability—batch after batch. Our teams, from purchasing to plant managers, have internalized that sense of pride. No flowchart or machine substitute stands in for eyes that notice a faint color difference, hands that recall yesterday’s pressure readings, or teams that catch a shift in the rate of drying overnight.

    We rely on facts gathered from years of production: the need for careful temperature control, the quirks of purification, and which storage containers stave off trace oxygen infiltration. Our job means solving problems before they become quality incidents. Every improvement in process, documentation, or delivery strengthens the value we bring to both researchers and formulation professionals worldwide.

    Supporting new discoveries depends not just on molecules shipped, but on the trust, insight, and dependability forged over years. Our expertise lies not in advertising volume or website imagery, but in knowing exactly how, and why, our 4-chloro-2-mercapto-6-(trifluoromethyl)benzimidazole stands apart from the crowd. From process to product, we remain committed to earning that trust, one batch at a time.