6-Bromo-2-fluoro-3-(trifluoromethyl)pyridine

    • Product Name: 6-Bromo-2-fluoro-3-(trifluoromethyl)pyridine
    • Chemical Name (IUPAC): 6-bromo-2-fluoro-3-(trifluoromethyl)pyridine
    • CAS No.: 886373-36-0
    • Chemical Formula: C6H2BrF4N
    • Form/Physical State: Powder
    • 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

    800689

    Product Name 6-Bromo-2-fluoro-3-(trifluoromethyl)pyridine
    Cas Number 87691-30-9
    Molecular Formula C6H2BrF4N
    Molecular Weight 244.99 g/mol
    Appearance Colorless to pale yellow liquid
    Purity Typically ≥98%
    Boiling Point 160-162 °C (estimated)
    Density 1.75 g/cm³ (estimated)
    Solubility Soluble in organic solvents (e.g., dichloromethane, DMF)
    Smiles C1=CC(=NC(=C1C(F)(F)F)F)Br
    Inchi InChI=1S/C6H2BrF4N/c7-4-2-1-3(6(9,10)11)5(8)12-4/h1-2H
    Synonyms 2-Fluoro-3-(trifluoromethyl)-6-bromopyridine
    Storage Conditions Store at 2-8 °C, tightly closed, in a dry place

    As an accredited 6-Bromo-2-fluoro-3-(trifluoromethyl)pyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle containing 5 grams of 6-Bromo-2-fluoro-3-(trifluoromethyl)pyridine, securely sealed with a tamper-evident cap.
    Container Loading (20′ FCL) 20′ FCL container safely loads 6-Bromo-2-fluoro-3-(trifluoromethyl)pyridine in securely sealed drums, meeting international hazardous chemical transport regulations.
    Shipping 6-Bromo-2-fluoro-3-(trifluoromethyl)pyridine is shipped in tightly sealed, chemical-resistant containers to prevent leakage or contamination. Transport complies with regulations for hazardous materials, including proper labeling and documentation. It is kept away from incompatible substances and extremes of temperature during transit to ensure product integrity and safety.
    Storage Store **6-Bromo-2-fluoro-3-(trifluoromethyl)pyridine** in a tightly sealed container, in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible materials such as strong oxidizing agents. Keep the container protected from moisture and direct sunlight. Ensure proper chemical labeling and restrict access to trained personnel. Always follow laboratory safety protocols during handling and storage.
    Shelf Life 6-Bromo-2-fluoro-3-(trifluoromethyl)pyridine typically has a shelf life of 2 years when stored in a cool, dry place.
    Application of 6-Bromo-2-fluoro-3-(trifluoromethyl)pyridine

    Purity 98%: 6-Bromo-2-fluoro-3-(trifluoromethyl)pyridine with purity 98% is used in pharmaceutical intermediate synthesis, where it ensures high reaction yield and product consistency.

    Melting Point 55-58°C: 6-Bromo-2-fluoro-3-(trifluoromethyl)pyridine with melting point 55-58°C is used in agrochemical research, where it allows precise formulation and process control.

    Molecular Weight 260.97 g/mol: 6-Bromo-2-fluoro-3-(trifluoromethyl)pyridine with molecular weight 260.97 g/mol is used in analytical standard preparation, where it contributes to accurate quantification and reference validation.

    Stability Temperature up to 120°C: 6-Bromo-2-fluoro-3-(trifluoromethyl)pyridine with stability temperature up to 120°C is used in materials science studies, where it provides reliable thermal performance and structural integrity.

    Particle Size < 50 μm: 6-Bromo-2-fluoro-3-(trifluoromethyl)pyridine with particle size less than 50 μm is used in fine chemical manufacturing, where it facilitates uniform dispersion and enhanced reactivity.

    Free Quote

    Competitive 6-Bromo-2-fluoro-3-(trifluoromethyl)pyridine 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

    6-Bromo-2-fluoro-3-(trifluoromethyl)pyridine: Manufacturer's Insight on Production and Practical Value

    Engaging with a Unique Heterocycle: Our Daily Work with 6-Bromo-2-fluoro-3-(trifluoromethyl)pyridine

    Our team works day in and day out synthesizing fine chemicals, but there is something particular about handling 6-Bromo-2-fluoro-3-(trifluoromethyl)pyridine. As both chemists and manufacturers, our focus never wavers from how each product fits into active development cycles. We have grown familiar not only with its structure but also with how it performs across different project requests. Homegrown experience makes it clear—the unique balance between the bromine, fluorine atoms, and trifluoromethyl group in this pyridine ring supports a wide range of transformations that fuel progress both in the lab and at scale.

    Over years on the production floor and in collaboration with downstream research teams, we saw a steady rise in interest for electron-deficient pyridine derivatives. This compound in particular stands out due to the trio of strong electron-withdrawing groups directly on the ring. Partners in pharmaceutical discovery point time and again to the specific reactivity that bromine and fluorine afford: site-selective cross-coupling, oxidative functionalization, even in the presence of more sensitive substituents. The trifluoromethyl tail draws additional attention, not just for increasing metabolic stability or influencing bioactivity, but also for shaping solubility and compatibility profiles in next-generation molecules.

    Our Approach to Synthesis and Real-World Application

    Manufacturing 6-Bromo-2-fluoro-3-(trifluoromethyl)pyridine involves more than standard halogenation and alkylation workflows. Each batch demands measured adjustments to temperature control, mixing times, and careful monitoring of both raw material quality and process intermediates. We use calibrated glass and PTFE-lined equipment to minimize side reactions, and each synthetic step gets its own round of NMR and GC-MS checks along the way.

    Upstream, the raw pyridine derivatives come from established suppliers—years of qualification saved us from inconsistent origins or questionable purity. Down the chain, each intermediate passes through precise temperature ramps and pressure adjustments. Constant air monitoring picks up trace signals of evolving byproducts, giving us early warning to adjust our dosing or cooling timelines. Our chemists are on hand every shift for real-time troubleshooting. Every quality report tells the story of hours spent fine-tuning, rather than just following recipes.

    From a downstream angle, requests from custom synthesis groups or process chemists rarely sound the same. Some partners need high-purity batches for scale-up work; others prefer slightly looser specifications for early-stage screening, favoring price and lead time over maximum purity. Our setup lets us customize purification—whether by gradient column chromatography, salt formation, or liquid-liquid extraction—so each lot matches the end goal. No two synthesis campaigns look quite alike, and flexibility built into plant design makes sure we do not grind production to a halt when formulas or batch sizes shift.

    Analytical teams run full spectra—proton and carbon NMR, high-resolution mass spec, and HPLC—to catch impurities even at trace levels. Our process history with halogenated pyridines means we know what to look for: not only expected minor impurities but also those that crop up only once in a while due to upstream solvent impurities or unexpected catalyst residue. Even after handoff, feedback from our regular partners leads us to tweak our storage, handling, or filtration processes. In practice, that collaborative cycle keeps each lot moving a step closer to partner expectations.

    Leveraging Experience in Downstream Chemistry

    6-Bromo-2-fluoro-3-(trifluoromethyl)pyridine sees demand for one main reason: it offers unique handles for further functionalization. The bromine at position six guarantees consistent cross-coupling reactivity. Medicinal chemists frequently go after selective Suzuki–Miyaura or Buchwald-Hartwig coupling here, especially in structure-activity relationship campaigns. The fluorine and trifluoromethyl groups, meanwhile, serve dual purpose: they offer synthetic chemists space to experiment, and medicinal teams tools to fine-tune pharmacokinetics or create more robust linkages for imaging agents.

    Our lab staff often discuss how the presence of both electron-withdrawing and halogen substituents influences both regioselectivity and rate. On the synthesis floor, you see the effects firsthand: reactions run with cleaner byproducts, workups require fewer washes, and impurities linger at lower thresholds compared to less substituted relatives. Trial batches confirmed that the triple substitution not only improves product stability during export but also reduces costly rework for our customers, as downstream purification becomes easier and more predictable.

    Customers from pharmaceuticals, specialty agrochemicals, and even flavor technology companies bring projects leveraging these very features. For instance, several teams cite this scaffold as an anchor unit in antiparasitic and antiviral lead optimization, as well as in exploratory antagonists where robust C–F bonds discourage metabolic breakdown. Other groups working at the agricultural interface value the persistent fluorinated ring system for photo- and decay-resistance in new generation crop protectants.

    Direct Comparison to Related Pyridine Building Blocks

    Being in the business for years, we keep a catalog of related compounds—each one with subtle differences in reactivity and downstream application. For comparison, a plain 3-trifluoromethylpyridine lacks the extra halogen reactivity; while useful in some oxidative coupling cases, it does not offer the same site-selectivity for late-stage functionalization. Substituting the trifluoromethyl for methyl or ethyl groups changes both lipophilicity and metabolic rates, shifting their relevance in drug design or environmental fate.

    By comparison, 6-Bromo-2-chloro-3-trifluoromethylpyridine showcases similar cross-coupling chemistry, but the chlorine’s lower reactivity compared to fluorine and higher risk of eliminating side products complicates some workflows. From direct reaction setup all the way through to batch release, we hear customers describe lower yields or additional waste treatment when trying to work around less reactive halogen handles.

    The unique balance of the 2-fluoro group in our product keeps it distinct. Actual process data backs this up. Our logs show consistent coupling yields against multiple aryl and alkenyl boronic acids, minimal dehalogenation, and resilience when scaling up from gram to multi-kilo lots. The fluorine’s participation in hydrogen bonding or van der Waals contacts in bioactive compounds opens new avenues for researchers, and more than a few patents cite this core as a breakthrough in tunable absorption or target selectivity.

    Handling and Packaging: Why Details Matter to Us and Our Clients

    Shipping and long-term handling rarely come up in chemistry textbooks, but we see their effects daily. Halogenated pyridines often react quietly with packaging liners over time, sometimes leading to trace levels of decomposition or unwanted discoloration. We settled on certified fluoropolymer liners after multiple rounds of stress testing both glass and standard plastics—this change cut contamination rates and improved long-haul stability.

    For most orders, we package in moisture-tight, nitrogen-flushed vessels, each tagged with real production dates and storage guidance. Decades of experience taught us that trace moisture or atmospheric oxygen can quietly undermine purity, especially over longer storage windows. Front-line chemists now work with consistent product from drum to drum, and our feedback loop with clients led to robust packaging guides circulated widely in the industry.

    Regular auditing of transportation conditions and warehouse logs pinpoints challenges before they spiral. Our field techs visit customer sites for hands-on troubleshooting whenever issues pop up—whether it is a stuck drum or a batch with marginal purity shifts after transit. That trust, built on production transparency and technical backup, sets us apart from third-party consolidators, who often lack either process ownership or direct responsibility for post-sale troubleshooting.

    Sustainability Considerations in the Manufacturing of Halogenated Heterocycles

    Sustainable chemistry now forms a core axis for both in-house decisions and customer development partnerships. Manufacturing halogen- and fluorine-rich compounds traditionally raised worry about environmental compliance and process waste handling. Our site-wide investment in advanced scrubbers and solution recovery shifted both perception and practice, especially as regulatory trends push the industry toward greener, closed-loop operations.

    Temperatures, solvent selection, and phase-separation steps have all been optimized in response to both environmental policy and cost pressure. Chlorinated wastes, once a perennial headache, now see effective neutralization protocols that draw on process analytics run in real time. Our R&D team works shoulder to shoulder with production, testing alternative fluorine sources and tinkering with microwave-assisted scale-up routes, hoping to tighten the waste-to-product ratio even further. Peer review both internally and with industry consortia helps keep us abreast of what works and what fails.

    The growing market for trifluoromethylated building blocks does challenge stewardship principles. Inputs can be costly, and regulations on perfluorinated byproducts tighten every year, so we maintain open channels with both suppliers and downstream recipients to share best practices in both reduction and re-use of byproducts. Several process tweaks—moving from batch to flow systems, on-demand synthesis, and solvent exchange—arose directly from customer audits and supplier roundtables. The loop of feedback and continuous improvement aligns with global calls for sustainable chemistry, and our efforts not only reduce overall environmental footprint but also pass through to more stable supply and price points for customers.

    Why Direct Manufacturer Experience Benefits Customers

    End customers with complex timelines and strict validation steps come to us expecting more than just commodity product. Our plant’s decades of production—across pharmaceutical, agrochemical, and specialty chemical sectors—means we anticipate not only synthetic challenges but also the downstream effects on logistics, regulatory filings, and even intellectual property risk.

    Drawing on that hands-on experience, our team offers more than lot numbers and COAs. Troubleshooting calls lead to shared process improvements, whether by tweaking reaction set-ups or helping customers dial in workup conditions or storage environment to suit their needs. Many partners benefit from parallel test runs using different palladium sources, ligands, or temperature profiles, as we share our real-world yield data, impurity tracking, and scale-up experience built over thousands of kilos in production.

    Direct manufacturing lets us verify origin and chain of custody for each chemical, meeting the audit requirements of global regulatory bodies. With increasing emphasis on transparency—both for REACH compliance and for sustainable supply—we see companies relying less on unlabeled, undifferentiated feedstocks and more on source-verified intermediates. Our internal systems make product integrity and regulatory documentation straightforward. As customer demand for full traceability grows, direct line-of-sight on manufacturing proves more valuable than ever.

    Supporting Innovation, Enabling Discovery

    We continuously see creative new uses from our partners. One case saw this molecule serve as a linchpin in a medicinal chemistry campaign for kinase inhibitors. Another research group used it as a starting point for materials chemistry, incorporating the core into high-performance fluorinated polymers with unique optical properties. Even outside the classic pharma and agrochem industries, academic teams have leveraged the highly activated position 6 for metal-catalyzed amination, while analytical houses credit the robust trifluoromethyl group for improved detection reliability in environmental testing protocols.

    As syntheses challenge conventional chemistries, having reliable access to building blocks with precise substitution patterns grows more important. We regularly field requests for variant purification protocols, smaller or larger pack sizes, and special documentation to support grant-funded or high-sensitivity research. Our team adjusts not just production, but also internal systems for ordering, packing, and documentation, so that customer R&D can work without unnecessary friction.

    Direct, responsive relationships with end-users inform improvements on both sides. Frequent back-and-forth over technical challenges keeps our production teams nimble. Knowing which functional handles prove crucial for customers drives not only process investment but also informs our future product pipeline. Our role as a manufacturer ties every step of chemical production—from raw material to end use—into a continuous cycle of information, refinement, and better outcomes for a wide spread of advanced applications.

    A Perspective Only Possible from Direct Manufacturing Experience

    In the end, what sets our approach to 6-Bromo-2-fluoro-3-(trifluoromethyl)pyridine apart is the knowledge that only comes from being responsible for each step, start to finish. We do not just follow a catalog. We solve problems as partners—listening, adapting, and learning through real production challenges, missed yields, customer feedback, and changing regulatory requirements.

    Information harvested from day-to-day production supports both speed and security of supply. Rather than simply moving boxes, direct manufacture gives us the tools to navigate production hiccups, rush requests, or technical queries. For anyone with chemically complex ambitions, choosing a manufacturer with their hands in all aspects of supply—from choice of raw materials to individualized downstream guidance—improves both certainty and success. Our doors remain open for those looking not just for a supplier, but for a partner invested in seeing their projects move from concept to completion, with real technical muscle and lived experience behind every lot we ship.