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2-Bromo-4-(Trifluoromethyl)Pyridine

    • Product Name 2-Bromo-4-(Trifluoromethyl)Pyridine
    • Alias 2-Bromo-4-(trifluoromethyl)pyridine
    • Einecs 249-003-7
    • 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
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    Specifications

    HS Code

    213903

    Product Name 2-Bromo-4-(Trifluoromethyl)Pyridine
    Chemical Formula C6H3BrF3N
    Cas Number 175205-82-4
    Molecular Weight 226.00 g/mol
    Appearance Colorless to pale yellow liquid
    Boiling Point 184-186 °C
    Melting Point -
    Density 1.73 g/cm³
    Purity Typically ≥98%
    Solubility Soluble in organic solvents
    Smiles C1=CN=C(C=C1C(F)(F)F)Br
    Inchi InChI=1S/C6H3BrF3N/c7-5-3-4(1-2-11-5)6(8,9)10/h1-3H
    Refractive Index n20/D 1.499
    Storage Temperature Store at 2-8 °C
    Synonyms 2-Bromo-4-(trifluoromethyl)pyridine; 4-(Trifluoromethyl)-2-bromopyridine

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

    Packing & Storage
    Packing A 25-gram amber glass bottle with a secure screw cap, labeled "2-Bromo-4-(Trifluoromethyl)Pyridine" and relevant hazard information.
    Shipping **Shipping Description:** 2-Bromo-4-(Trifluoromethyl)Pyridine is shipped in tightly sealed containers, protected from moisture and light. It is classified as a hazardous chemical and must be handled according to relevant transport regulations. Appropriate labeling and documentation are included, and temperature controls may be applied to ensure product stability during transit.
    Storage Store 2-Bromo-4-(trifluoromethyl)pyridine in a tightly sealed container in a cool, dry, and well-ventilated area, away from heat, moisture, and incompatible substances such as strong oxidizers. Protect from direct sunlight. Ensure all handling is in compliance with local regulations, and use appropriate personal protective equipment to avoid contact or inhalation. Keep container properly labeled and out of reach of unauthorized personnel.
    Application of 2-Bromo-4-(Trifluoromethyl)Pyridine

    Applications of 2-Bromo-4-(Trifluoromethyl)Pyridine in Industrial Manufacturing

    2-Bromo-4-(Trifluoromethyl)Pyridine serves as an advanced synthetic intermediate in several high-value industrial sectors. As a direct manufacturer, we supply this compound for specialty chemical synthesis across pharmaceutical, agrochemical, and electronics industries, where its reactivity, purity, and traceability are prioritized for specific downstream applications.

    1. Active Pharmaceutical Ingredient (API) Intermediate Synthesis

    Leading pharmaceutical manufacturers rely on this material in the preparation of modern heterocyclic drug molecules, especially for molecules targeting CNS and oncology indications. The compound enters the synthesis route for potent drug candidates featuring pyridine scaffolds, where it undergoes key steps including Suzuki coupling and further nucleophilic substitutions. Its high chemical stability under GMP-controlled environments ensures batch reproducibility and trace impurity control in API production. Applications typically involve multi-step synthesis, where stringent quality and traceability requirements apply due to regulatory submissions.

    Industry compliance standards

    • ICH Q7 GMP for APIs
    • USP/NF monograph requirements for final APIs
    • 21 CFR Part 210/211 cGMP
    • EU GMP EudraLex Vol. 4

    Typical usage ratio

    • 0.5–1.2 molar equivalents, adjusted per desired yield and target molecule complexity

    Downstream process integration

    • Charged in initial or mid-stage heterocyclic coupling steps, mainly palladium-catalyzed cross-couplings or Grignard reactions during multi-kilo batch synthesis

    Final product types

    • Pharmaceutical drug substance (API)
    • Clinical trial material (CTM) for research and preclinical use
    • Regulatory reference standards

    2. Agrochemical Active Ingredient Manufacturing

    Agrochemical producers utilize this intermediate for the synthesis of selective herbicides and insecticides, often where advanced fluorinated heterocycle cores are required for mode-of-action selectivity. This compound provides a stable brominated pyridine ring, facilitating N-alkylation or arylation to introduce active functional groups. It enables downstream formulation chemistry for crop protection products by supporting diverse reactivity patterns and purity levels suitable for environmental and residue analysis.

    Industry compliance standards

    • OECD GLP for chemical synthesis and product testing
    • FAO/WHO specifications for pesticide active ingredients
    • ISO 9001 Quality Management System

    Typical usage ratio

    • Used at 0.7–1.0 molar equivalent per target molecule in batch synthesis; actual ratio depends on further functionalization and downstream coupling partner

    Downstream process integration

    • Used as an aryl bromide synthon during construction of active ingredient core before formulation into technical grade products

    Final product types

    • Post-patent herbicide active substances
    • Systemic insecticide precursors
    • Analytical reference compounds for residue testing

    3. Electronic Chemicals for Liquid Crystal and OLED Materials

    Display and semiconductor manufacturers employ this compound for synthesizing highly specialized pyridine-based monomers needed for high-performance liquid crystal and OLED emitter materials. The reactivity and electron-withdrawing character of the trifluoromethyl group allow precision tuning of final product voltage thresholds and stability. The controlled introduction of this intermediate enables the reproducible production of high-purity fine chemicals essential to panel and device performance, where ppm-level impurity handling is critical for manufacturing yields.

    Industry compliance standards

    • RoHS Directive 2011/65/EU for electronic components
    • IEC 62474 Material Declaration for electronic assemblies
    • SEMICON Quality guidelines

    Typical usage ratio

    • Typically 0.3–0.5 molar ratio as a ring-functionalization intermediate, tuned according to optical or thermal performance targets

    Downstream process integration

    • Input at the heterocyclic monomer synthesis stage for subsequent polymerization into liquid crystal or small-molecule OLED precursors

    Final product types

    • OLED emitter intermediates
    • Specialty liquid crystal monomers
    • High-performance display material additives

    4. Fluorinated Building Block for Fine Chemical Synthesis

    Industrial fine chemical companies source this compound as a building block for synthesizing advanced materials such as specialty dyes, catalysts, and custom ligands, leveraging its halogen and trifluoromethyl functionalities. Its structure supports regioselective functionalization via cross-coupling or nucleophilic substitution, enabling the design of custom-engineered molecules for advanced material science, analytical chemistry, and research markets. Quality and traceability are critical in this segment, with custom batch processing and customer-specific quality documentation.

    Industry compliance standards

    • ISO 9001 Quality Management System
    • REACH Regulation (EC) No 1907/2006 for imported/exported chemicals
    • GLP for analytical reference materials

    Typical usage ratio

    • Varies from 0.1 to 2.0 equivalents dependent on end molecule design and yield targets

    Downstream process integration

    • Introduced during the core structure assembly phase, prior to specific end-use modifications, in pilot or production scale fine chemical synthesis

    Final product types

    • Fluorinated custom ligands
    • Specialized analytical reference standards
    • Advanced dye and catalyst intermediates
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    Certification & Compliance
    More Introduction

    2-Bromo-4-(Trifluoromethyl)Pyridine: How a Versatile Pyridine Building Block Elevates Chemical Synthesis

    Understanding the Role of 2-Bromo-4-(Trifluoromethyl)Pyridine in Modern Chemistry

    In the world of heterocyclic chemistry, few units carry the reliability that pyridine rings offer. Since we started manufacturing 2-Bromo-4-(Trifluoromethyl)Pyridine, its impact became clear in both laboratory and industrial-scale reactions. The compound introduces specific reactivity and selectivity, essential traits we have recognized while working closely with medicinal chemists, agrochemical developers, and R&D teams across the globe.

    This pyridine derivative offers a precise blend: the bromo substituent at position 2 creates a reactive center primed for further functionalization, while the trifluoromethyl group at position 4 packs a punch for electronic modulation. Our experience shows this combination proves highly valued in cross-coupling strategies, namely Suzuki, Buchwald-Hartwig, and Stille reactions. These methods demand consistent starting materials that maintain performance under varying batch scales. By monitoring every step of our own chlorination, bromination, and fluorination lines, we’ve kept contaminant levels low and returns high for years.

    Molecular Formula, Batch Purity, and Real-World Handling

    2-Bromo-4-(Trifluoromethyl)Pyridine appears as a colorless to pale yellow liquid or sometimes off-white solid, depending on storage conditions or shipment. Maintaining control over temperature and moisture during both synthesis and packaging keeps the product in optimal form. Internal QC checks apply gas chromatography and NMR to every batch, consistently verifying chemical identity, purity, and the absence of free bromide or isomeric byproducts.

    The structure, with a molecular formula of C6H3BrF3N and a typical purity of not less than 98 percent by HPLC, strikes a balance between reactivity and stability. Years of hands-on experience show it stores well under inert atmosphere — many of our partners move product directly from sealed drums to automated dosing lines, reducing possible contamination. While glass bottles work well for sampling, full-scale lots rely on high-density poly drums with tight seals.

    Performance Metrics: Why Electronic Effects Matter

    Much of the interest in this product comes from the trifluoromethyl group’s electron-withdrawing nature. In practice, that means reaction partners — especially nucleophiles or coupling agents — respond with different kinetics and selectivity. For chemists aiming to introduce complex fragments or maintain delicate stereochemistry, this characteristic widens the strategic options. On our side, we’ve collaborated on process optimization spanning pilot to kiloton scale, and have watched how fine-tuning those electronic effects reduces sidereactions and improves final yields.

    One major difference from non-fluorinated or non-halogenated pyridines: the enhanced lipophilicity. This property proves crucial for SAR (structure-activity relationship) studies in drug design, and time after time the feedback from end-users points toward the value it brings for passing biological membranes. In our workshops with synthetic teams, discussion often revolves around how switching from a methyl to trifluoromethyl moiety in this backbone sharpens both potency and transport properties in target molecules.

    Real-World Applications: Beyond Standard Alkylations and Arylations

    Pharmaceutical companies lean heavily on this intermediate for the development of kinase inhibitors, antiviral agents, and novel CNS drugs. Technical review sessions reveal many projects deploying site-selective coupling at the bromo position, expanding molecular diversity fast. Agrochemical formulators, in contrast, tap into its reactivity for new herbicides and fungicides where robust field activity and metabolic stability matter. Batching reports often show how reaction progress tracks smooth and reproducible across both 10 L and 10,000 L reactors.

    Specialty material developers see another side: embedding this motif into OLED or display technologies, benefiting from both the nitrogen atom and the fluorinated ring. It delivers a level of tuning not easily reached using more traditional six-membered aromatics. Our past collaborations included scale-ups for pigment and dye intermediates, where this building block provided precisely the set of physical and electronic parameters needed.

    Comparative Notes: How It Differs from Related Pyridines

    Among bromopyridines, adding the trifluoromethyl at position 4 sets this molecule apart. Its electron-withdrawing power goes beyond what you’d get from 2-bromopyridine alone or from analogs with simpler alkyl groups. Some industrial clients once tried substitutes like 2-bromo-6-methylpyridine or even 4-chloro-2-bromopyridine, yet lacked the yield jump and the selectivity achieved with our trifluoromethyl variant. Analytical follow-up confirmed much tighter control over mono-substitution and fewer side-chain rearrangements.

    Our direct customers often comment on how the CF3 group makes purification and final formulation easier — organofluorine tags improve volatility profiles and instrumental detectability, facts borne out in both pilot reports and internal stress tests. Comparing with unsubstituted bromopyridines, the boost to chemical stability and resistance to oxidative degradation becomes especially significant for long-storage APIs or active intermediates destined for international shipment.

    Process Integration: Challenges We Have Solved

    Each scale-up project brings its own lessons. Early on we faced issues with controlling bromination at low temperatures, since the pyridine ring likes to substitute at multiple positions. We adapted by using specially purified solvent systems and in-line temperature probes for each reactor line, allowing tight control over exotherms — essential for larger runs where a misstep can cost an entire batch.

    Trifluoromethyl installation created its own hurdles due to the aggressive reagents and strong bases involved. By shifting to continuous-flow fluorination in some stages, and fully enclosing the discharge points, we managed to minimize operator risk and cut process cycle times. These changes allowed us to supply multi-metric-ton consignments with repeatable lot-to-lot quality. Problems like color changes or phase separation, once frequent, nearly disappeared after this process update.

    Why Quality Assurance Makes or Breaks Product Value

    Some manufacturers still treat bench and plant-scale production as distinct territories. From our site, everything links together: feedback from end-users, analytic data, material handling logistics, and storage stability results all directly impact future synthesis runs. Consistency drives value. Each container carries not just a chemical, but a history of attention to detail that our technicians have rigidly enforced.

    In practice, this means pulling real-world impurity profiles from chromatographs of production lots. Heavy reliance on on-site NMR, GC-MS, and moisture analyzers lets us intervene early and prevent overbromination, contamination with free halides, or potential pyridine isomer interferences. Our teams monitor every lot for chemical and physical stability over several months — vital steps, since clients report smoother downstream processing and negligible crystallization failures.

    Environmental and Safety Considerations from a Manufacturer’s Perspective

    Making high-performance halopyridines always involves chemical risks. Over the years, our safety protocols evolved to match the challenges of large-scale bromination and fluorination. Most current installations run fully enclosed, with automated scrubbers removing airborne halides before venting. Our solvent recovery units shrink emissions and recycle nearly eighty percent of organic wash solvents into the next cycle — a move that satisfies both regulatory and profit goals.

    Reactor and packaging staff use PPE, full-hood ventilators, and remote digital controls for transfer, confirming in-lab that concentrations stay well below exposure thresholds. Routine drills prepare both operators and engineers for unusual situations. Returns from regulatory audits show our track record keeps meeting — and often exceeding — environmental benchmarks. By treating byproduct waste with rigorous neutralization and recycling protocols, we minimize our landfill burden and keep groundwater uninfluenced, even as yearly output grows.

    Traceability and Documentation: Meeting the Demands of Downstream Auditors

    Traceability once seemed an afterthought, back when laboratories prioritized speed. Now, every package leaves our facility with digital certificates, analytical data, batch processing logs, calibration details, and storage histories — all immediately available for client and auditor review. Each year, audit teams from pharmaceutical and agrochemical partners visit to inspect our traceability practices. They see real-time data covering every raw material, every environmental test, and every handoff between departments.

    Our clients appreciate avoiding delays in regulatory filings or IP protection due to missing paperwork or disputed specs. On several occasions, project partners have communicated surprise at how rapidly we resolve documentation questions and supply analytical backup. This transparency shortcut translates to faster screening of lead compounds and fewer obstacles during scale-up trials.

    Logistics: Details That Support Scale, Quality, and Reliability

    Shipping halogenated pyridines worldwide brings specific challenges, especially since many regions regulate hazardous goods with tight tolerances on container strength and labeling. In response, we design custom transport drums and UN-rated canisters that stand up to bumpy transit and temperature extremes, and we run logistics checks for each region’s customs forms.

    Timing matters too: delays at port, excessive dwell times, or improper storage can spoil an entire consignment and eat into everyone’s margins. We coordinate closely with partner warehouses and forwarders to prevent temperature spikes and handling errors. Our partners offer candid feedback — this open loop helps tighten all stages, from batch release to end-user delivery.

    Innovation and Supply Readiness: Bringing Lab-Scale Discovery to Global Access

    Feedback from research teams guides us in expanding specifications. Some customers ask for higher-purity grades, free-flowing crystalline formats, or specialty packaging for automated dosing robots. Our R&D crew regularly tweaks our production lines for better scalability, updating protocols to match the ways our material gets used in rapidly changing synthetic pathways. Lab-scale insights often uncover new demand — especially as novel pharmaceuticals and crop protectants call for nonstandard heterocycles.

    Investments in process intensification have allowed us to meet surges in demand when screening hits deliverable leads and an early-stage project rapidly expands to pilot or commercial scale. Sharing our technical notes, troubleshooting guides, and QC procedures with downstream partners raises their confidence and shortens timelines for route scouting. By remaining flexible and honest about capabilities, we keep customer timelines predictable amid supply chain uncertainty.

    Future Trends: The Expanding Role of Fluorinated Building Blocks

    Chemistry, much like technology, continues to evolve. Drug discovery increasingly prizes molecules that pack both metabolic stability and controllable reactivity. Agrochemical regulations favor compounds that break down in targeted ways, without persistent impact on soil or water. OLED and electronic material specialists now hunt for fine-tuned, functionalized aromatics that perform under tougher service conditions.

    2-Bromo-4-(Trifluoromethyl)Pyridine fits squarely into these new requirements. It provides a dependable scaffold for further diversification, high resistance to oxidative stress, and unique reactivity profiles compared to traditional halopyridines. Through next-gen analytical instruments and stricter supply metrics, we plan to push these boundaries ever wider.

    By staying in touch with chemists, process engineers, supply teams, and regulatory auditors, we keep aligning our products with the emerging needs of each field. This approach shapes every drum, every batch, and every document we ship, reinforcing the trust needed for long-term collaboration.

    Conclusion

    The story of 2-Bromo-4-(Trifluoromethyl)Pyridine is still being written by every chemist, process line, and manufacturer who chooses reliable, tightly controlled building blocks. By maintaining hands-on oversight and refining each part of production, we deliver a compound that continues to reshape synthetic possibilities in pharmaceuticals, agrochemicals, materials, and specialties. Working up close with our customers, always adapting and documenting, keeps us ready to tackle tomorrow’s chemical challenges, whatever form they take.