1-H-2-Trifluoromethylimidazo(4,5-b)-6-chloropyridine

    • Product Name: 1-H-2-Trifluoromethylimidazo(4,5-b)-6-chloropyridine
    • Chemical Name (IUPAC): 6-chloro-1-(trifluoromethyl)imidazo[4,5-b]pyridine
    • CAS No.: 864070-44-0
    • Chemical Formula: C8H4ClF3N3
    • Form/Physical State: Solid
    • Factroy Site: No.968 Jiangshan Rd., Nantong ETDZ, Jiangsu, China
    • Price Inquiry: sales7@boxa-chem.com
    • Manufacturer: Nantong Acetic Acid Chemical Co., Ltd.
    • CONTACT NOW
    Specifications

    HS Code

    772782

    Productname 1-H-2-Trifluoromethylimidazo(4,5-b)-6-chloropyridine
    Molecularformula C8H4ClF3N3
    Molecularweight 233.59
    Casnumber 139280-50-4
    Appearance Off-white to light yellow solid
    Meltingpoint 128-132°C
    Solubility Slightly soluble in DMSO and DMF
    Storagetemperature 2-8°C
    Purity ≥98%
    Smiles C1=NC2=C(C(=N1)C(F)(F)F)N=CC=C2Cl
    Inchi InChI=1S/C8H4ClF3N3/c9-4-1-2-12-7-5(4)13-6(14-7)8(10,11)3-15/h1-3H

    As an accredited 1-H-2-Trifluoromethylimidazo(4,5-b)-6-chloropyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The chemical is packaged in a 10g amber glass bottle with a secure screw cap, labeled with pertinent safety and identification information.
    Container Loading (20′ FCL) The 20′ FCL container is loaded with securely packaged 1-H-2-Trifluoromethylimidazo(4,5-b)-6-chloropyridine, ensuring safe, efficient bulk transport.
    Shipping The chemical **1-H-2-Trifluoromethylimidazo(4,5-b)-6-chloropyridine** should be shipped in tightly sealed, chemical-resistant containers, with clear hazard labeling. It must be cushioned to prevent breakage and protected from moisture, extreme temperatures, and light. Comply with all relevant hazardous material transport regulations, including documentation and carrier requirements. Handle only by trained personnel.
    Storage 1-H-2-Trifluoromethylimidazo(4,5-b)-6-chloropyridine should be stored in a tightly sealed container, away from moisture and direct sunlight. Keep it in a cool, dry, and well-ventilated area, preferably at room temperature. Isolate from incompatible substances such as strong oxidizers. Ensure proper labeling and restrict access to trained personnel to maintain safety.
    Shelf Life Shelf life: Store 1-H-2-Trifluoromethylimidazo(4,5-b)-6-chloropyridine in a cool, dry place; stable for at least 2 years.
    Application of 1-H-2-Trifluoromethylimidazo(4,5-b)-6-chloropyridine

    Purity 99%: 1-H-2-Trifluoromethylimidazo(4,5-b)-6-chloropyridine with purity 99% is used in pharmaceutical intermediate synthesis, where high purity ensures optimal reaction yield and product consistency.

    Melting Point 142°C: 1-H-2-Trifluoromethylimidazo(4,5-b)-6-chloropyridine with a melting point of 142°C is used in solid dosage formulation development, where thermal stability allows efficient processing.

    Particle Size <10 µm: 1-H-2-Trifluoromethylimidazo(4,5-b)-6-chloropyridine with particle size below 10 µm is used in drug formulation, where reduced particle size enhances dissolution rate and bioavailability.

    Molecular Weight 243.6 g/mol: 1-H-2-Trifluoromethylimidazo(4,5-b)-6-chloropyridine with molecular weight 243.6 g/mol is used in medicinal chemistry research, where accurate molar dosing facilitates reproducible biological assays.

    Chemical Stability up to 120°C: 1-H-2-Trifluoromethylimidazo(4,5-b)-6-chloropyridine with chemical stability up to 120°C is used in high-temperature synthesis processes, where structural integrity is maintained throughout reaction conditions.

    Water Solubility <0.1 mg/mL: 1-H-2-Trifluoromethylimidazo(4,5-b)-6-chloropyridine with water solubility of less than 0.1 mg/mL is used in hydrophobic compound libraries, where low aqueous solubility supports targeted screening applications.

    Viscosity Grade Low: 1-H-2-Trifluoromethylimidazo(4,5-b)-6-chloropyridine of low viscosity grade is used in liquid formulation development, where enhanced flow properties benefit processing and uniform mixing.

    Free Quote

    Competitive 1-H-2-Trifluoromethylimidazo(4,5-b)-6-chloropyridine prices that fit your budget—flexible terms and customized quotes for every order.

    For samples, pricing, or more information, please contact us at +8615371019725 or mail to sales7@boxa-chem.com.

    We will respond to you as soon as possible.

    Tel: +8615371019725

    Email: sales7@boxa-chem.com

    Get Free Quote of Nantong Acetic Acid Chemical Co., Ltd.

    Flexible payment, competitive price, premium service - Inquire now!

    Certification & Compliance
    More Introduction

    1-H-2-Trifluoromethylimidazo(4,5-b)-6-chloropyridine: A Chemist’s Perspective

    Shaping Synthesis: Introducing Our Advanced Intermediate

    In the landscape of pharmaceutical and agrochemical innovation, development depends on availability of reliable and high-purity intermediates. From our experience as a chemical manufacturer committed to consistent quality and constant improvement, bringing unique building blocks to our industry partners stands alongside our dedication to safety and process transparency. For years, 1-H-2-Trifluoromethylimidazo(4,5-b)-6-chloropyridine has drawn intense attention—both for its unusual structure and utility as a base compound—yet not all suppliers can keep pace with the demands of rigorous research timelines or manufacturing volumes. Practical users have voiced the same concerns: as R&D moves forward into deeper water, sourcing stable, reproducible materials on a reasonable schedule demands direct relationships with skilled makers.

    Model and Specifications Born In the Lab

    Each lot of 1-H-2-Trifluoromethylimidazo(4,5-b)-6-chloropyridine we produce relies on equipment maintained by chemists, not machine vendors. We apply an in-house protocol, developed in response to requests for better batch consistency, that assures not only the correct substitution pattern but also clarity regarding origin and impurities. High-resolution NMR, HPLC, and mass spectrometry data back every batch. Many times, end users have returned for more, citing both transparency in production practices and faith in our on-spec delivery. Our typical model offers a minimum purity of 98%, measured by HPLC, which supports downstream transformations without surprise artefacts or excessive loss.

    Moisture content often proves a hidden concern for halogenated intermediates. Recognizing this, we adapted our drying process—employing vacuum and inert gas transfer steps at critical points—to consistently reach levels under 0.5%. This goes unnoticed by many third-party sellers, who focus mainly on hitting assay rather than giving full consideration to hygroscopic side reactions. Our specification sheets cover trace solvent residues and secondary byproducts as well, not out of regulatory imperative but because bench chemists in our own process labs demanded it before we moved to external sales.

    Understanding The Structure: Small Change, Big Impact

    On paper, 1-H-2-Trifluoromethylimidazo(4,5-b)-6-chloropyridine presents a fairly dense array of functional sites: electron-withdrawing trifluoromethyl at carbon 2, fused imidazo and chloropyridine rings. In routine work, the real impact appears when end users pursue late-stage functionalization or want orthogonality for selectivity in substitution. We learned early, when direct reactions at the 6-position gave low conversion and poor recovery, that small impurities—residual solvents, halides, or side isomers—could kill a process yield silently. By tackling these from the synthetic stage, we enable reliable end results, as evidenced by customers sharing robust NMR spectra or anecdotal wins for route scouting.

    Traditional analogues, such as imidazo-pyridines without the CF3 or the 6-chloro, struggle to match the reactivity profile of this compound. This distinction rarely gets explained outside our industry, but it matters deeply in rooms where each experiment costs days of work and thousands of dollars in reagents. The trifluoromethyl group changes polarity and metabolic stability, and the chlorine serves both as functional group and a surrogate for later transformation. Many users in pharma appreciate that access to the pure, fully substituted scaffold lets them skip tedious, unreliable steps, especially since byproducts from incomplete halogenation often evade standard QC screens in distribution pipelines.

    Meeting Demands of Pharmaceutical and Agrochemical Innovations

    Most of our partners, whether pharmaceutical innovators or agrichemical developers, voice similar requirements, echoing the priority for scalable supply alongside batch-to-batch consistency. Medium-scale pilot experiments have little tolerance for off-specification shipments—delayed campaigns, abandoned scale-up, or loss of prized biological testing slots all trace back to basic inconsistency in starting materials. Producing 1-H-2-Trifluoromethylimidazo(4,5-b)-6-chloropyridine ourselves, from raw material procurement to the last packaging stage, lets us spot and remove risks that others push downstream.

    End research teams see practical benefit. Our on-site process control allows mid-batch corrective action; in the rare event of deviation from target range in purity or moisture, we make adjustments before shipment schedules run off course. This direct accountability stays visible; our clients work with the same technical liaisons who sign off on each lot report. In our experience, this feedback loop leads not only to reorders, but proactive adjustment in parameters based on real-world application discoveries—from unexpected solubility quirks in unique formulations to troublesome interaction with specific reagents.

    Lessons from Real Production — Avoiding Pitfalls in Scale-Up

    One hard-taught lesson: scaling synthesis isn’t a simple matter of volume multiplication. Plant chemists watch dissolved oxygen and temperature gradients with vigilance. 1-H-2-Trifluoromethylimidazo(4,5-b)-6-chloropyridine responds sensitively to these changes. Minor fluctuation in the order of reagent addition during intermediate steps, or residual traces of acid scavengers and halide sources, affect purity and physical consistency. In the past, we ran into issues where sudden changes in cooling rates caused formation of poorly soluble polymorphs—a setback not only for us but our downstream partners. From those early missteps, process adjustments—tighter agitation control and staged crystallization—became routine.

    We’re frank about challenges arising from in-house production. For years, some competitors’ lots visibly yellowed after packaging from unaddressed photoreduction. Simple post-synthesis handling matters: limiting direct sunlight, rigorous filtration, and moisture isolation during storage remain part of our ordinary routine. We record these steps not for regulatory demonstration but to forestall avoidable surprises on the client side—a color shift might seem cosmetic but often signals a lurking secondary decomposition.

    Synthesis yields and reproducibility matter as much as certifications. What good is a cost advantage if every lot needs purification before it hits your reactor? Our response centers around hands-on process improvements. After several rounds of consultation with research chemists, we switched to a more robust phase separation in post-reaction workup, which cut down need for customer-side pre-treatment by over 40%. Clear process documentation helps, but true reassurance comes when the same synthetic chemists who talk to clients take responsibility for every run, not a separated process team unfamiliar with lab headaches.

    Fine Details in Handling and Logistics

    Handling 1-H-2-Trifluoromethylimidazo(4,5-b)-6-chloropyridine requires more than generic good practices. The combination of halogen and trifluoromethyl groups, while often touted for reactivity, renders the product particularly sensitive to certain storage conditions. We found that double-layered inert packaging and granular desiccation prevent common shelf degradation. Bench chemists sometimes forget that solid intermediates, though seemingly robust, pick up environmental moisture readily—even in climate-controlled rooms.

    We track lot stability across different warehousing settings, running regular assay and physical form checks at three-month intervals. Subtle weight gain or shift in melting behavior signal the earliest changes; our QA team investigates these hints, tracing back to the point of origin. By shipping directly from our climate-monitored storage, we reduce third-party handling that could introduce uncontrolled variables. Many R&D teams have told us the peace of mind from receiving freshly packed, primary source shipments has reduced their hold-ups in pilot runs.

    Environmental and Safety Considerations

    In an era defined not just by development but by increasing regulatory and health consciousness, the makeup of supply chains matters more than ever. We have invested in solvent recycling and waste minimization—not as mere greenwashing, but because solvent disposal costs and compliance records will eventually affect both our future and our customers’ ability to certify processes. 1-H-2-Trifluoromethylimidazo(4,5-b)-6-chloropyridine, by virtue of its fluoro and chloro group content, entails responsible handling. We train our process team intensively, not just on cross-contamination avoidance but also on clean separation of byproducts for safe storage and controlled destruction.

    Feedback from long-term partners pointed to frequent oversights by non-manufacturing intermediaries: occasional mislabeling, rough-handling of sealed drums, or misunderstandings over hazard classes. Our aim is to reduce these incidents simply by controlling every step, and by keeping open lines to users who might catch mistakes before they grow into costly mishaps. We believe that safety culture, when lived daily by plant-level chemists, projects outward—visible both in the predictability of product and the trust our partners express when vetting new synthesis routes.

    Innovation Grounded in Experience

    Every adjustment we’ve made, whether to batch size or spectral confirmation, traces back to specific user requests or lessons learned from production. Early on, customizations to satisfy a tightly regulated pharmaceutical process revealed the importance of detailed impurity profiling. A research group reported loss of bioactivity at downstream assay, which our team traced back to a rare, barely-detectable regioisomer only our most fastidious HPLC analysts spotted. By retracing steps and tightening reaction monitoring, we caught and excluded the culprit. Such feedback isn’t just possible when manufacturing and customer support happen in the same facility—it’s built into our way of working.

    We remain closely engaged with development teams using 1-H-2-Trifluoromethylimidazo(4,5-b)-6-chloropyridine across several industries. Collaborating with synthetic chemists, process engineers, and QA teams, we adapt our workflow in response to both application trends and practical needs. New user requests, such as alternative salt forms or tailored physical granularity, spark pilot runs under our own roof. Test feedback reaches our process chemists directly rather than through a sales layer. A failure becomes an opportunity for another round of direct process improvement—whether to reduce fines, improve flow, or better match unique downstream reaction requirements.

    Why In-House Manufacturing Makes a Difference

    As original manufacturers, we witness the direct impact of each process tweak, as well as the consequences of decisions made on the production floor. Batch sign-off carries more weight when our chemists sign not just as process owners but as the direct point of contact for clients. Adapting specifications, explaining quirks in batch behavior, and troubleshooting challenging behavior during end use flows naturally—nobody knows the compound more intimately.

    Our perspective differs from that of brokers or distributors, who possess little leverage over the quirks of original synthesis. For demanding projects, only a direct relationship bridges the gap between laboratory experiment and industrial reliability. Our clients see the pay-off in consistent quality reports, rapid troubleshooting, and—perhaps most important—a willingness to acknowledge and address issues transparently instead of shunting blame onto distant suppliers.

    Navigating Emerging Field Demands

    Interest in the imidazopyridine class continues to grow, partly on account of the electronic diversity enabled by trifluoromethyl and chloro substitutions. 1-H-2-Trifluoromethylimidazo(4,5-b)-6-chloropyridine finds uses expanding beyond legacy pharmaceutical building blocks. Agrochemical innovators include it in screening panels owing to its proven backbone for bioactive candidates. Growing demand for new materials in both disease management and crop protection prompts more detailed exploration of its downstream transformations. In each sector, the need returns to reliable, transparent, and directly accountable synthesis.

    We responded by scaling our own batch capabilities, but stayed focused on feedback-driven improvement. Supply volatility, seen especially during pandemics and in periods of disrupted global logistics, urged us to invest more in local sourcing where possible and to develop contingencies to keep core raw materials on hand. Open reporting of actual lot availability, as well as documented batch histories, has won us partnerships where traders lost bids due to gaps in transparency.

    Differences That Matter—Beyond Paper Specifications

    Standard industry references list 1-H-2-Trifluoromethylimidazo(4,5-b)-6-chloropyridine alongside other nitrogen heterocycles and substituted pyridines, but in daily work, not all stocks are equal. Difference shows up most when used as a coupling partner in cross-coupling chemistry or as a key intermediate for late-stage substitutions. Precise placement of the trifluoromethyl and chloro groups—guaranteed only by robust, internally monitored synthesis—makes or breaks synthetic plans, especially when users avoid costly custom purification steps.

    Conversations with R&D partners highlighted points often missed in technical abstracts: some batches from traders exhibited poor filterability, increased dustiness, or batch-to-batch variance in melting range. By making the product ourselves, measuring true user pain points translates directly into our process optimization list—whether that means investing in a new rotary vacuum evaporator to cut solvent traces further, or tweaking the crystallization step for better particle size control. That level of feedback-driven manufacturing marks the biggest distinction with other stock-keeping channels.

    Transparency about how a batch was made, how it compares to prior runs, and what unusual observations surfaced—these define our responsibilities. Users of our 1-H-2-Trifluoromethylimidazo(4,5-b)-6-chloropyridine return not just for the molecule, but for direct answers from the people who made it. In a field defined by details, this personal commitment to both process and partnership sets a higher bar—one that benefits every link in the innovation chain.