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2-Bromo-3-Trifluoromethylpyridine

    • Product Name 2-Bromo-3-Trifluoromethylpyridine
    • Alias 2-Bromo-3-(trifluoromethyl)pyridine
    • Einecs 251-882-2
    • 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

    760082

    Productname 2-Bromo-3-Trifluoromethylpyridine
    Casnumber 87691-87-0
    Molecularformula C6H3BrF3N
    Molecularweight 225.99
    Appearance Colorless to pale yellow liquid
    Boilingpoint 193-195°C
    Meltingpoint -
    Density 1.668 g/mL at 25°C
    Purity Typically ≥98%
    Refractiveindex n20/D 1.507
    Synonyms 2-Bromo-3-(trifluoromethyl)pyridine
    Smiles C1=CC(=C(N=C1)Br)C(F)(F)F
    Inchi InChI=1S/C6H3BrF3N/c7-5-2-1-4(6(8,9)10)3-11-5/h1-3H
    Solubility Soluble in organic solvents
    Storagetemperature Store below 30°C

    As an accredited 2-Bromo-3-Trifluoromethylpyridine 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 2-Bromo-3-Trifluoromethylpyridine, sealed with a screw cap and labeled for laboratory use.
    Shipping 2-Bromo-3-Trifluoromethylpyridine is shipped in tightly sealed containers, protected from light and moisture. It is handled as a hazardous material, complying with applicable regulations for chemical transport. Shipping includes proper labeling, safety documentation, and may require temperature control to ensure the compound's stability and prevent degradation during transit.
    Storage 2-Bromo-3-Trifluoromethylpyridine should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from sources of heat or ignition. Keep it away from incompatible substances such as strong oxidizers and strong acids. Protect the chemical from moisture and direct sunlight. Ensure proper labeling and follow all relevant safety and regulatory guidelines for storage.
    Application of 2-Bromo-3-Trifluoromethylpyridine

    Applications of 2-Bromo-3-Trifluoromethylpyridine in Industrial Manufacturing

    As an established producer of 2-Bromo-3-Trifluoromethylpyridine, we supply this key intermediate to multiple downstream sectors that rely on rigorous quality control, industry compliance, and precise formulation processes. Below, we outline the principal industrial applications, providing concrete details on integration points, relevant regulatory standards, technical usage ratios, and the range of finished products our clients manufacture using this raw material.

    1. Agrochemical Synthesis: Active Ingredient Intermediates for Herbicides

    Crop protection manufacturers utilize 2-Bromo-3-Trifluoromethylpyridine as a building block for synthesizing pyridine-based herbicidal active substances. Its halogenated pyridine structure offers critical reactivity for producing selective systemic herbicides designed for cereal and broadleaf crops. Production requires strict batch control and comprehensive traceability to fulfill agrochemical industry obligations.

    Industry compliance standards

    • FAO/WHO Specification and Evaluations for Agricultural Pesticides
    • OECD Guidelines for the Testing of Chemicals (Synthesis/Characterization)
    • EU Regulation (EC) No 1107/2009 (Plant Protection Products)
    • ISO 9001:2015 (Quality Management Systems for Agrochemical Manufacturing)

    Typical usage ratio

    • 5–12% by molar ratio in the heterocyclization stage, adjusted by the targeted yield of herbicidal active compounds and impurity control requirements

    Downstream process integration

    • Introduced during the initial halopyridine coupling reactions, followed by further functionalization and purification to yield technical concentrate of the herbicide

    Final product types

    • Active ingredient concentrates (AI)
    • Water-dispersible granules (WDG)
    • Suspension concentrates (SC)
    • EC (emulsifiable concentrate) formulations for field application

    2. Pharmaceutical Intermediate for Anti-Infective Drug Development

    Pharmaceutical manufacturers incorporate this compound as a core pyridine intermediate in the synthesis of fluorinated heterocyclic scaffolds, which serve as critical structures in the production of clinical candidates for anti-infective drugs. GMP-compliant facilities track every batch for regulatory inspections and toxicological traceability, reflecting the stringent nature of pharmaceutical supply chains.

    Industry compliance standards

    • ICH Q7 (Good Manufacturing Practice for Active Pharmaceutical Ingredients)
    • 21 CFR Part 211 (cGMP for Finished Pharmaceuticals)
    • USP–NF standards for API quality
    • Ph. Eur. (European Pharmacopoeia) guidelines for intermediate purity

    Typical usage ratio

    • 8–15% relative to the main pyridine precursor in regulated route selection, with adjustments for batch scale-up and impurity profile requirements

    Downstream process integration

    • Added during the nucleophilic aromatic substitution or bromination steps, forming a reactive intermediate for further functional group elaboration, purification, and heterocycle assembly

    Final product types

    • Advanced pharmaceutical intermediates
    • Active pharmaceutical ingredient (API) candidates for antibiotics/antivirals
    • Clinical trial comparator supplies

    3. Fine Chemicals: Synthesis of Specialty Fluorinated Pyridines

    Chemical manufacturers use 2-Bromo-3-Trifluoromethylpyridine in the production of high-purity specialty pyridines, where precision fluorination and bromination support the custom development of chemical libraries for discovery and high-value products. Quality control emphasizes low residual solvents and lot-specific analytical characterization for demanding clients in specialty chemistry.

    Industry compliance standards

    • ISO 9001:2015 (Organics Chemicals Manufacturing)
    • REACH Regulation (EC) No 1907/2006 for industrial chemical substances
    • GLP (Good Laboratory Practice) for analytical chemical production

    Typical usage ratio

    • 10–18% as part of multi-step synthetic routes, choice adjusted based on target fluorine content and custom molecule specifications requested by end-users

    Downstream process integration

    • Added as a halogenated nucleophile in cross-coupling/metal-catalyzed reactions, immediately followed by distillation or column purification to isolate target pyridine compounds

    Final product types

    • Specialty fluorinated pyridines for research
    • Intermediates for custom organic syntheses
    • Reference standards and analytical reagents

    4. Electronic Chemicals: Precursor for Liquid Crystal Materials

    The electronics materials sector incorporates this compound into multi-step syntheses of liquid crystal intermediates, which provide the molecular backbone for display technologies like TFT-LCDs. This route demands exceptional product consistency, strict metal impurity control, and compliance with industry-specific cleanroom production regulations.

    Industry compliance standards

    • IEC 61340 (ESD Control in Electronics Manufacturing)
    • JEITA Quality Requirements for Electronic Chemicals
    • ISO/TS 16949 (Quality Management for Automotive Electronics)
    • RoHS Directive (2011/65/EU) restricting hazardous impurities

    Typical usage ratio

    • 7–13% within the nucleophilic substitution stage, refined per the targeted polarity and birefringence of the liquid crystal compound

    Downstream process integration

    • Charged into the synthesis reactor prior to subsequent condensation and purification steps, followed by liquid–liquid extraction and, if required, high-vacuum distillation for trace impurity removal

    Final product types

    • Intermediate mixtures for TFT-LCD liquid crystals
    • High-purity monomers for display-grade liquid crystal alignment agents
    • Advanced organic materials for optoelectronic integration
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    Certification & Compliance
    More Introduction

    Introducing 2-Bromo-3-Trifluoromethylpyridine: A Manufacturer’s Perspective

    At our facility, quality and understanding come from direct experience with every batch and every raw material. 2-Bromo-3-Trifluoromethylpyridine (CAS No. 270112-05-7) has become one of the most interesting compounds in our synthetic lineup, and our team has handled its production from raw reactants up to kilo-scale lots. Right from the start, process safety, purity screening, and reliable supply have guided our approach. There’s no shortcut through the hands-on work that shapes a consistently well-made chemical.

    What Sets 2-Bromo-3-Trifluoromethylpyridine Apart

    Making halogenated pyridine derivatives shows just how much small changes in structure matter to practical outcomes. Bringing a trifluoromethyl group into the molecular ring, alongside a bromo substituent, delivers a compound valued by research chemists, agrochemical formulators, and medicinal chemistry groups looking to push known scaffolds in new directions. Every run through our reactors reinforces why this molecule keeps a spot on so many project checklists.

    Structurally, the compound falls into the class of substituted pyridines. The presence of both a bromine atom and a trifluoromethyl group at adjacent positions on the ring leads to electronic effects that drive selective reactivity in further synthesis. It’s tough to overstate how much of a control this gives to chemists building complex molecules—the electron-withdrawing CF3 group pulls activity in a way that allows for targeted transformations downstream. Compared to simpler bromo-pyridines or trifluoromethyl-pyridines alone, the dual substitution pattern delivers an upgrade in terms of reaction versatility.

    We can trace the demand for this compound back to its core utility as an intermediate. Whether for coupling reactions, cross-couplings, or metal catalysis, its use as a building block pops up in patents and literature covering everything from crop protection agents to kinase inhibitors. In all these routes, the role of the starting material’s purity and consistency affects not only final product yield, but also rework and troubleshooting further down the line. We’ve taken that lesson to heart in how we standardize our specs and process controls.

    Manufacturing Experience: Key Steps and Challenges

    Nobody sees more than the team working on the plant floor, running 2-Bromo-3-Trifluoromethylpyridine through glass-lined vessels and refining its isolation. Controlling reaction exotherms and halogen handling has taught everyone to respect the chemistry and act accordingly. Our typical production sequence uses 3-Trifluoromethylpyridine as a basis, introducing bromine under strictly regulated temperature and solvent conditions. Correct order of addition and agitation speeds aren’t just theoretical—they mark the difference between efficient product formation and unwanted byproduct.

    Our chemists avoid cut-corners on washing steps and drying regimens, not only for purity’s sake, but to ensure no trace brominated side products slip through. Analytical checks focus on GC and NMR profiles before any material moves to storage. Physical refinements, such as crystallization or distillation, are verified batch-wise by the team that’s witnessed off-target colors, foaming, or stability shifts firsthand. By the time material is packed, we know it intimately from vessel to vessel.

    Product Specifications from a Practical Angle

    Though datasheets capture melting points, GC purities, and NMR spectra, real-world performance springs from experience. Over multiple lots, our process delivers material that meets a minimum of 98% GC purity, and is free from residual starting materials and common halogenated impurities at levels well below 1%. These aren’t just marketing claims—our QC analysts hold each batch to these thresholds to avoid cascade problems in downstream synthesis reported by previous campaign feedback.

    We know some users prefer a technical grade, while others demand stricter controls for sensitive pharmaceutical intermediates. Our long-term clients have taught us that flexibility at the specification and packaging stages answers the bulk of project needs. If a medicinal chemist needs sub-ppm levels of certain contaminants, we can run extra purification cycles or provide additional characterization data. For agrochemical process teams focused on scale and cost-effectiveness, speed and volume take precedence, so larger drums with rapid batch delivery become more important than trace purity enhancements.

    Handling and Storage Practices

    As with most halogenated heterocycles, 2-Bromo-3-Trifluoromethylpyridine should be kept sealed, cool, and dry to maintain chemical integrity. Those who have stored kilogram units for months know that slow breakdown doesn’t pose much threat—but preventing introduction of moisture and avoiding contact with incompatible materials such as strong bases guards against avoidable waste and equipment contamination. Our recommendation, built from warehouse experience, sticks to the basics: use clean, airtight containers (preferably amber glass or HDPE), store at ambient temperature out of sunlight, and check for any physical changes periodically.

    We always caution that, while the compound’s volatility remains moderate, open transfers or extended exposure can cause loss over time. In the production environment, we’ve implemented closed-system handling wherever possible, reducing vapor exposure for operators and extending material shelf life. As a team that’s seen spills result in operational delays and product loss, these steps are more than a compliance checklist—they’re the groundwork for smooth order fulfillment.

    Usage in the Field: What Our Clients Teach Us

    Over the past decade, most of our 2-Bromo-3-Trifluoromethylpyridine lots have ended up in discovery and early process optimization labs. Clients in fine chemicals and pharma research groups report using this compound as a precursor for Suzuki, Stille, or Buchwald–Hartwig cross-coupling reactions, especially when crafting molecules that require tailored electronic or steric control on a pyridine backbone. Direct amination and arylation routes, in particular, benefit from the electron-deficient nature of the ring once both the bromine and trifluoromethyl groups are present.

    A critical advantage, often cited by synthetic chemists, lies in the way this molecule opens access to further substituted pyridines with both fluorinated and aryl or alkyl functions. For instance, some project teams use our product to create advanced intermediates for new herbicide formulations, where the CF3 group imparts metabolic stability and alters biological activity profiles. Others in drug development exploit its unique substitution pattern to build molecules with altered solubility or target selectivity. Not every bromo-pyridine serves this niche—only those with well-controlled impurity profiles and reproducible performance in coupling chemistry remain consistently favored in client projects.

    Why Not Just Use Similar Compounds?

    One question we hear from some new customers concerns using other, more commonly available mono-substituted pyridines, or those carrying just a trifluoromethyl or just a bromo group. In lab tests and scale-up campaigns, though, the limits become obvious. While single-substituted pyridines may offer lower cost or easier handling, the dual substitution in 2-Bromo-3-Trifluoromethylpyridine unlocks a reactivity window not accessible with those simpler versions. Unwanted side reactions or the need for additional protection/deprotection steps often surface with more basic precursors.

    A clear example: attempts to achieve the same synthetic endpoint starting from non-fluorinated rings typically reduce final yields and load more complexity onto purification stages. Meanwhile, unhalogenated CF3-pyridines lack a handle for further functionalization, locking out key modifications. Our in-house process design team tracks these issues closely, consulting with downstream users and running side-by-side comparisons, so we continue to supply the version that answers real-world synthetic challenges.

    Trust and Traceability in Every Batch

    Rarely do labs walk away with only a product—they take with them a set of expectations shaped by trust and repeated experience. Our production logs stretch back years, tracing every lot from incoming raw material analysis to shipment. We maintain retained samples, perform regular staff training on handling and hazard controls, and keep thorough documentation in a format accessible to clients with regulatory or transparency questions.

    False positives in quality control or spotty documentation don’t just threaten compliance—they risk entire project timelines. Over the years, we’ve seen how close technical relationships with advanced users improve their troubleshooting and allow us to refine our own processes. Often, a rejected shipment or a flagged impurity report leads to an update in our analytical techniques or supplier audits. None of these lessons come from standard operating procedures alone—they’re the product of shared history between our teams and our customers’ labs.

    Looking Ahead: Continuous Improvement and Collaboration

    Steady advances in coupled catalytic chemistry bring new use cases and stricter requirements each year. As more complex molecules move from discovery to pre-commercial scale, the feedback loop between our plant chemists, analytical group, and end-users grows only tighter. Whether it’s tweaking solvent choices to avoid cross-contamination, reducing residual metal catalysis artifacts in the material, or refining storage advice to line up with regional logistics, improvements come directly from hands-on manufacturing and customer interaction.

    We invest heavily in both technical training and method development, recognizing that it’s not enough to meet a baseline standard if projects keep growing in complexity. As new environmental and regulatory expectations arrive, our process teams stay ahead by upgrading containment systems, automating hazardous transfers, and extending our trace-level impurity monitoring.

    Potential Solutions to Key Industry Issues

    Supply certainty and safety emerge as the two primary concerns for most partners using specialty pyridine derivatives. Years managing everything from raw supply constraints to unexpected regulatory changes have taught us that close upstream and downstream communication limit disruptions. For example, maintaining secondary suppliers for core starting materials and building buffer inventories at critical stages enable us to weather shipping delays or raw material quality swings.

    Safety improvements spring from process engineering and operational discipline. Installing local exhaust and automated dosage controls, for example, shrinks exposure risk during bromination. Continuous staff education and in-line monitoring prevent most potential incidents before they develop. Each time we introduce a new SOP, it’s because there’s a specific, practical lesson behind the update—often coming directly from those who work with the compound every day.

    We recognize that as the environmental profile of chemical manufacturing comes under sharper scrutiny, traceability, closed waste handling, and resource efficiency must become part of the solution set. By investing in solvent recycling, emission capture, and product lifecycle data, we not only answer today’s requirements but prepare for demands on future transparency and accountability. Taken together, these steps ensure every kilogram of 2-Bromo-3-Trifluoromethylpyridine moving from our site reflects care for both chemistry and community.

    Why Experience Matters in Specialty Chemical Manufacturing

    Looking over the span of our involvement with pyridine derivatives, the path hasn’t always run smooth. Process upsets, unexpected reactivity, and learning through setbacks have shaped both our facility and our people. Each technical improvement—whether in analytical resolution, reactor cleaning, or customer communication—anchors itself in the discipline that repeated large-scale production imparts. It’s one thing to read papers or data sheets about a compound; it’s another to see how real-world process changes echo in every part of the supply chain.

    Partnership with skilled and demanding clients keeps us vigilant. New synthetic strategies emerge every year, and nobody gets to coast on reputation. The strongest signal we receive is the steady return of project teams that value open dialogue, flexible supply, and steady product quality that doesn’t slip over time. By sharing both successes and failures openly, our team embodies what it takes to keep specialty building blocks like 2-Bromo-3-Trifluoromethylpyridine reliable—no matter how complex demands and applications become.

    Conclusion: Supplying More Than a Product

    Every delivery of 2-Bromo-3-Trifluoromethylpyridine marks the intersection of chemistry, production know-how, and trust earned through years of attention to detail. Beyond the molecule itself, we supply confidence backed by traceable processes, responsive support, and a record of active, ongoing improvement. As innovation in chemicals accelerates, our experience provides the foundation for both existing and future applications—a resource that only grows more important as the landscape continues to evolve.