5-bromo-2-trifluoromethyl pyridine

    • Product Name: 5-bromo-2-trifluoromethyl pyridine
    • Chemical Name (IUPAC): 5-bromo-2-(trifluoromethyl)pyridine
    • CAS No.: 349087-15-8
    • Chemical Formula: C6H3BrF3N
    • Form/Physical State: Liquid
    • Factroy Site: No.968 Jiangshan Rd., Nantong ETDZ, Jiangsu, China
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    • Manufacturer: Nantong Acetic Acid Chemical Co., Ltd.
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    Specifications

    HS Code

    528818

    Chemical Name 5-Bromo-2-(trifluoromethyl)pyridine
    Molecular Formula C6H3BrF3N
    Molecular Weight 225.00 g/mol
    Cas Number 85118-33-8
    Appearance Colorless to pale yellow liquid
    Boiling Point 192-194°C
    Melting Point -2°C
    Density 1.719 g/cm³
    Refractive Index 1.509
    Purity ≥98% (typical)
    Flash Point 72°C
    Solubility Slightly soluble in water; soluble in organic solvents
    Smiles C1=CC(=NC=C1Br)C(F)(F)F
    Storage Conditions Store in a cool, dry place, tightly closed

    As an accredited 5-bromo-2-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 25 grams of 5-bromo-2-trifluoromethyl pyridine, sealed with a white screw cap and labeled with hazard warnings.
    Container Loading (20′ FCL) 20′ FCL holds about 12MT of 5-bromo-2-trifluoromethyl pyridine, packed in 200 kg iron drums or HDPE drums.
    Shipping **Shipping Description:** 5-Bromo-2-trifluoromethyl pyridine is shipped in secure, airtight containers to prevent leakage or contamination. It is transported as a hazardous chemical, complying with relevant safety regulations (such as UN and IATA guidelines). Proper labeling, documentation, and temperature control are ensured to maintain product integrity during transit.
    Storage 5-Bromo-2-trifluoromethyl pyridine should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from direct sunlight and incompatible substances such as strong oxidizing agents. Keep it away from sources of ignition and moisture. Store at room temperature and clearly label the container. Follow all standard laboratory chemical storage guidelines to ensure safety.
    Shelf Life 5-Bromo-2-trifluoromethyl pyridine is stable for at least two years if stored in a cool, dry, and dark place.
    Application of 5-bromo-2-trifluoromethyl pyridine

    Purity 99%: 5-bromo-2-trifluoromethyl pyridine with 99% purity is used in pharmaceutical intermediate synthesis, where it ensures high yield and minimal impurities in active ingredient production.

    Melting Point 53°C: 5-bromo-2-trifluoromethyl pyridine with a melting point of 53°C is used in custom heterocycle preparation, where controlled fusion enables precise reaction conditions.

    Stability Temperature 120°C: 5-bromo-2-trifluoromethyl pyridine exhibiting stability up to 120°C is used in high-temperature coupling reactions, where thermal resistance maintains product integrity.

    Molecular Weight 244.98 g/mol: 5-bromo-2-trifluoromethyl pyridine with a molecular weight of 244.98 g/mol is used in medicinal chemistry workflows, where exact dosing and stoichiometry are critical for reproducibility.

    Particle Size <50 µm: 5-bromo-2-trifluoromethyl pyridine with a particle size less than 50 micrometers is used in catalyst screening platforms, where fine dispersion enhances reaction rates.

    Moisture Content <0.5%: 5-bromo-2-trifluoromethyl pyridine with moisture content below 0.5% is used in anhydrous organic synthesis, where low hygroscopicity prevents side reactions.

    Assay (HPLC) ≥98%: 5-bromo-2-trifluoromethyl pyridine with an assay result of ≥98% by HPLC is used in regulated process development, where analytical purity meets stringent quality standards.

    Residual Solvent <100 ppm: 5-bromo-2-trifluoromethyl pyridine containing less than 100 ppm residual solvent is used in agrochemical active development, where minimal solvent traces ensure product safety and compliance.

    Refractive Index 1.554: 5-bromo-2-trifluoromethyl pyridine with a refractive index of 1.554 is used in optical material research, where consistent optical properties facilitate screening studies.

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    Certification & Compliance
    More Introduction

    5-Bromo-2-trifluoromethyl Pyridine: Stepping Forward in Modern Research and Industry

    A chemical name can seem remote and intimidating, but to someone who spends their working days in the lab, substances like 5-bromo-2-trifluoromethyl pyridine have meaning that goes far beyond a formula. I remember the first time I came across this compound; a colleague walked into our research space holding a slim bottle labeled in tidy black letters. He handed it to me with the easy confidence of someone who understood its role: a mindful tool, not a mystery. I’ve looked at it differently since then, seeing in it a quiet promise that modern chemistry brings to medicine, material science, and the search for new technology.

    What Sets 5-Bromo-2-Trifluoromethyl Pyridine Apart

    5-bromo-2-trifluoromethyl pyridine stands out in the world of organic intermediates. The pyridine ring, easy to draw but full of complexity in its electronic structure, finds a regular spot in pharmaceuticals, agrochemicals, and advanced materials. This compound introduces both a bromine and a trifluoromethyl group to the pyridine core, creating a powerful combination—bromine for its reactivity in cross-coupling reactions, trifluoromethyl for its influence on metabolic stability and biological activity. Laboratories value it for this dual presence; it streamlines synthesis paths and allows researchers to explore chemical spaces otherwise harder to reach.

    Most of us in this field have a feel for tiny differences. Change a methyl group for a trifluoromethyl, or add bromine instead of chlorine, and you open a new door: a drug becomes more resilient, an agrochemical more precise, a material more suited to a hostile environment. It’s no accident that the trifluoromethyl group pops up everywhere in new pharmaceuticals—the CF3 cluster resists breakdown in the body, supporting drug stability and bioavailability. Add bromine at the right position on the pyridine ring and the molecule suddenly becomes an anchor point for Suzuki-Miyaura or other coupling reactions, connecting the core with new molecular partners.

    Specifications and Real-World Handling

    As someone who routinely works with heteroaromatics, the practical specifications of a compound often shape daily decisions. 5-bromo-2-trifluoromethyl pyridine comes pure—high-performance liquid chromatography (HPLC) confirms this, backing up the manufacturer’s claims with sharp peaks and clear baselines. Excess water or side-products can trip up later steps, so seeing a dry, crystalline solid or a clear, colorless liquid makes a difference. An accurate melting point gets more than a passing glance, especially for compounds that might degrade or polymerize with heat.

    Mass spectrometry and NMR readings confirm not just the identity but the quality that industrial partners or academic groups rely on. Precise weighing and careful transfer, gloves on and fume hood sash down, form part of the daily ritual. There’s nothing romantic about the burnt-plastic smell or the catch at the back of your throat from poorly purified chemicals. High-grade material means confidence, and confidence means one less variable in a sea of potential pitfalls. When a project rides on a single key reaction, these little details—the right registry numbers, a certificate of analysis, a clean shipping bottle—become more than bureaucratic demands; they protect months of effort.

    Differentiation in the Market

    In a world overflowing with chemical intermediates, 5-bromo-2-trifluoromethyl pyridine keeps earning its place on order sheets. Supply-side differences matter: some pyridine derivatives arrive murky or discolored, a sign of incomplete manufacture or poor handling. Others might carry a price premium without a matching purity boost.

    What sets this compound apart from similar pyridines—such as 2-bromo-5-trifluoromethyl pyridine or 2-chloro-5-trifluoromethyl pyridine—is the unique positioning of both substituents. Reactivity shifts depending on where you place those groups. For example, Suzuki or Buchwald-Hartwig reactions rely on the presence and position of a leaving group like bromine. Put it in the wrong place on the ring and yields can drop or the sought-after product may never appear. The trifluoromethyl group tailors electronic effects, influencing both how other reactants approach the ring and how stable the result remains. Compared to its chlorine-containing cousin, the bromo version often reacts faster and with a wider scope of coupling partners.

    Some manufacturers aim for simple economy, cutting corners on process controls or shipping times. I’ve received shipments of similar compounds from bulk suppliers that showed up clumped together, reeking of solvent, or growing crystals of who-knows-what inside weeks of uncareful storage. Reliable sources for 5-bromo-2-trifluoromethyl pyridine mean fewer headaches for every downstream user, from the synthetic chemist trying to build a new molecular scaffold to a plant manager watching the clock on a pilot run. I’ve moved from skepticism to trust after working with suppliers whose QC labs actually keep up with expectations—consistency from gram to kilogram.

    Role in Research and Industry

    In drug discovery labs, the search for new candidates never stands still. I’ve sat through meetings where teams agonize over whether to pursue one synthetic route or another, worried about how easy a new fragment can be built up, how stable it will remain, or whether a particular modification could add precious months of shelf life. The presence of a trifluoromethyl group often tips the scales toward a new analog, given the performance boost it often brings. Placing both bromine and trifluoromethyl on a pyridine ring creates options for multiple parallel syntheses, letting teams chase a promising lead from several angles.

    The agricultural world benefits just as much. Crop protection agents require durability in the field—rain, sunlight, soil microbes, and temperature swings punish the average molecule. At the same time, regulatory bodies continue to raise the bar for environmental and human safety. 5-bromo-2-trifluoromethyl pyridine forms the backbone of compounds that stick around only until the job is done, then break down predictably. Newer herbicides and fungicides depend on these building blocks for controlled release or target selectivity. The compound’s structure helps bridge the gap between effectiveness and environmental stewardship—a balance that keeps food supply chains running smoothly.

    Material scientists, too, draw value from chemistry that favors clean, precise reactivity. Electronic devices need materials that withstand heat, light, and chemical stress. Introducing fluorine—a mainstay of electronic-grade polymers—brings resilience and performance. By starting from a molecule already outfitted with both bromine and trifluoromethyl, engineers can build up specialty polymers or add ends that bond onto silicon, carbon, or metallic surfaces. Precision here means devices last longer and perform more reliably, a win for everything from flexible displays to wearable medical sensors.

    Quality and Reliability: Real-World Impact

    The mistakes of history show what happens when standards slip. Too often, researchers see momentum evaporate as batches from different suppliers fail to overlap in quality. I’ve lost count of the hours spent rerunning reactions, adding yet another column purification step, or freezing progress because a new shipment didn’t behave like its predecessor. That’s why a reputation for reliability counts—end users depend on transparency and an audit trail for every batch. Certificates of analysis, access to batch records, and customer service that actually answers technical questions win long-term loyalty. Scientific integrity relies not just on invention but on reproducibility, and this compound’s growing reputation owes much to consistent quality standards.

    The lessons extend beyond the lab. Industry sees real losses when delays in the supply chain or inconsistent batches ripple through a manufacturing campaign. Imagine the cost of shutting down a reactor for a week while engineers troubleshoot mystery by-products or chase down contamination sources. Reliable offerings allow companies to plan confidently, reducing storage space for backup lots and freeing capital for innovation instead of emergency fixes. The right chemical done right lubricates the machinery of discovery and production.

    Demand Drivers and Market Trends

    Demand for 5-bromo-2-trifluoromethyl pyridine keeps growing, and it’s not just the big pharmaceutical or agrochemical names driving it. Contract research organizations, academic startups, and specialty materials labs all play a role. The recent uptick in green chemistry initiatives, stricter regulatory environments, and an insatiable hunger for more effective molecules add fuel to this demand.

    I’ve watched peers in both startup culture and established R&D groups pivot toward scaffolds like this when faced with pressure to deliver something new and valuable. Launching an environmentally safer pesticide, or a pharmaceutical less prone to rapid metabolism, often means returning to the basics of scaffold design. Many teams have abandoned longer, more wasteful syntheses in favor of routes enabled by coupling chemistry, made possible by the bromo group’s presence. What seems a subtle tweak on paper—a new group at a single point on a six-membered ring—can unlock entire classes of new compounds, sometimes renewing expired patents or dodging metabolic pitfalls uncovered by toxicologists.

    The shift toward fluorinated molecules, especially those containing pyridine, finds backing in peer-reviewed journals and patent filings. Market reports point to double-digit growth in demand for specialized pyridine intermediates that contain both electron-rich and electron-poor regions, good news for those leveraging the unique profile of 5-bromo-2-trifluoromethyl pyridine. The compound sits comfortably between affordability and performance, not yet rare enough to attract speculative pricing but sufficiently useful to appear in advanced catalogs worldwide.

    Challenges and Pathways Forward

    No product is without its pain points. Handling brominated pyridines requires both care and good infrastructure. The best setups include robust extraction, proper containment, and regular maintenance; less prepared labs risk contamination or accidental exposure. I’ve seen the results of poor discipline—discoloration in finished compounds, unexpected reactivity leading to failed syntheses, safety scares that shake the team’s confidence. Still, broader adoption means more labs have professionalized their workflows, adopting better ventilation, improved training, and real-time environmental monitoring.

    Sustainability represents another challenge, one often discussed at industry conferences or tucked into the regulatory checklists. Manufacturing trifluoromethylated compounds can demand energy-intensive steps or use feedstocks with complicated histories. Bringing green chemistry principles to pyridine derivative manufacture forms part of current research efforts. More efficient methods for introducing the trifluoromethyl group—sometimes through direct fluorination, other times by flow chemistry or photoredox catalysis—begin to show promise. These routes often cut waste and reduce reliance on hazardous intermediates, holding out hope for cleaner production cycles alongside cost savings.

    Waste management bears mention as well. Labs and factories generate spent solvents and by-products that call for careful disposal. I learned early on to keep my own glassware scrupulously clean and to segregate halogenated waste from everything else. Better recycling options for solvents and improved downstream treatment processes now give end-users more options for staying compliant with both company ethics and government regulations. As a result, the environmental footprint of specialty pyridine derivatives shrinks year by year, a trend to nurture with each new process improvement.

    What Investors and End-Users Should Watch

    For those looking to invest in production or consumption of pyridine intermediates, vigilance pays off. Markets reward reliability and innovation, sometimes suddenly, and chemical landscapes can shift overnight with a regulatory ruling or scientific discovery. A few trends stand out. First, closer ties between end-users and suppliers lead to better feedback loops—lab techs and plant managers no longer hesitate to report issues, ask for better purity, or request tailored packaging. Second, the push for sustainability, already visible in the largest producers, ripples outward to mid-size and boutique operations, driving adoption of better waste handling, renewable feedstocks, and green synthesis routes.

    Supply chain resiliency, a hot topic since recent disruptions in global trade, receives fresh attention. Diversified sourcing and clear labeling now matter as much as bulk pricing, reflecting risk aversion and a premium on long-term relationships. Customers want to know not just what’s in the drum or bottle, but where it came from, how it was manufactured, and what trace substances ride along. By meeting these expectations, both legacy and upstart manufacturers maintain relevance and secure a stake in futures otherwise clouded by uncertainty.

    The rest of us—scientists, engineers, and consumers—watch these changes shape the products we use, the medicines we rely on, and the food we eat. I never expected to care much about the minutiae of paperwork or shipping protocols, but the weight of responsibility and the memory of lost hours spent on avoidable errors drove the lesson home. Chemistry works best out in the open, with transparency and accountability, and 5-bromo-2-trifluoromethyl pyridine offers a clear example of an intermediate that rewards careful handling and honest dealing.

    Envisioning Better Solutions

    It’s not enough to praise or critique what’s on offer; solutions emerge from addressing today’s shortfalls. For 5-bromo-2-trifluoromethyl pyridine, these solutions often blend chemistry with logistics and policy. Improved synthesis protocols promise higher yields with fewer side-products, supporting both laboratory and industrial scale-ups without ballooning costs. More manufacturers now invest in continuous flow reactors, which not only increase efficiency and consistency but also reduce the manual handling risks that have plagued older batch processes.

    Collaboration between academia and industry brings development cycles down to earth. Students and postdocs innovate in coupling methodology, solvent reduction, and green halogenation, feeding practical ideas into the commercial mainstream. Regulatory changes could do even more to reward these innovations—tax incentives for lower-emission factories, faster review cycles for sustainable feedstocks, and clear standards for trace impurities would all encourage more responsible production.

    Retailers and brokers also carry responsibility. Clearer, more detailed documentation, batch-level traceability, and responsive technical support form core expectations in today’s market. Each advance in tracking or transparency protects both sellers and buyers, anchoring relationships in trust rather than mere transaction. The smart combination of logistics and laboratory know-how defines the leaders in this field.

    Overall, 5-bromo-2-trifluoromethyl pyridine stands not as a static commodity but as a dynamic driver of science and technology. It teaches lessons—tough ones about quality, supply, waste, and opportunity—and inspires hope for better solutions born of clear-eyed experience. Each bottle or drum represents not just molecules, but a network of decisions, risks, and wins. In that story, researchers, manufacturers, and end-users all have a voice. Their collective efforts will shape where this versatile compound heads next, both within the lab and far beyond it.