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3-Bromo-2-Chloro-5-Fluoropyridine

    • Product Name 3-Bromo-2-Chloro-5-Fluoropyridine
    • Alias 3-Bromo-5-fluoro-2-chloropyridine
    • Einecs 816-111-6
    • 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

    209590

    Productname 3-Bromo-2-Chloro-5-Fluoropyridine
    Casnumber 863329-66-0
    Molecularformula C5H2BrClFN
    Molecularweight 210.44
    Appearance Colorless to pale yellow liquid
    Purity Typically ≥98%
    Boilingpoint 224-226°C
    Density 1.77 g/cm³
    Solubility Insoluble in water; soluble in organic solvents
    Smiles C1=C(C=NC(=C1F)Br)Cl
    Inchi InChI=1S/C5H2BrClFN/c6-4-2-8-5(7)1-3(4)9
    Refractiveindex 1.573 (estimated)
    Storagetemperature Store at 2-8°C
    Hazardclass Irritant

    As an accredited 3-Bromo-2-Chloro-5-Fluoropyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 25g of 3-Bromo-2-Chloro-5-Fluoropyridine is supplied in a sealed amber glass bottle with a printed hazard warning label.
    Shipping 3-Bromo-2-Chloro-5-Fluoropyridine is shipped in tightly sealed containers under inert atmosphere, protected from moisture and light. This chemical is transported according to all applicable regulations for hazardous materials, including proper labeling and documentation. Ensure compatible packaging and avoid contact with incompatible substances during shipping to guarantee safety and chemical integrity.
    Storage 3-Bromo-2-Chloro-5-Fluoropyridine should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from direct sunlight. Keep away from incompatible substances such as strong oxidizers and acids. Store at room temperature, avoiding moisture and heat sources. Ensure proper chemical labeling and restrict access to trained personnel only. Use appropriate personal protective equipment when handling.
    Application of 3-Bromo-2-Chloro-5-Fluoropyridine

    Applications of 3-Bromo-2-Chloro-5-Fluoropyridine in Industrial Manufacturing

    3-Bromo-2-Chloro-5-Fluoropyridine serves as a specialized halogenated pyridine intermediate utilized in several highly regulated downstream industrial sectors. With precise halogen substitutions, this compound plays a critical role in the synthesis of high-value end products, enabling fine-tuned process control in target molecule assembly. Below, we present in-depth application scenarios grounded in real-world chemical manufacturing, each with detailed compliance guidelines, formulation ratios, process integration steps, and finished product examples.

    1. Pharmaceutical Active Ingredient Synthesis

    Our material sees widespread use as a key pyridine core in the synthesis of selected pharmaceutical intermediates, particularly within respiratory and anti-infective therapeutics. The halogenation pattern supports late-stage functionalization and regioselective coupling reactions that underpin several regulated drug substance manufacturing processes. Downstream manufacturers rely on our consistent purity to maintain reproducible yields and straightforward impurity profiling, crucial in regulated pre-GMP and GMP API workflows.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • EU GMP Part II “Basic Requirements for Active Substances”
    • USP-NF monographs for relevant pyridine derivatives
    • European Pharmacopoeia (Ph. Eur.) raw material quality guidelines

    Typical usage ratio

    • 0.2–0.5 molar equivalents in key pyridine-coupling stages, adjusted based on target API substitution pattern
    • Variations depend on the synthetic route—commonly 15–25% weight/weight in intermediate formation batches

    Downstream process integration

    • Feeds into stepwise amination, Suzuki-Miyaura, or Buchwald–Hartwig cross-coupling reactions for precursor modification
    • Introduced post-nitrogen protection in multi-step API syntheses to minimize halide side-product generation

    Final product types

    • NCE (new chemical entity) APIs for respiratory and anti-infective drugs
    • Regulatory-submitted intermediates for global clinical trial supplies
    • Final small-molecule drug substances for on-market therapeutics
    • Advanced pharmaceutical intermediates (APIs-in-progress)

    2. Agrochemical Active Compound Development

    The substance provides an ideal halogenated pyridine scaffold for R&D and scale-up in the crop protection sector. Agrochemical companies use it to develop selective herbicide and insecticide active ingredients, leveraging the electron-withdrawing halogens to tailor molecular activity and stability. Production lines demand tight quality assurance to address batch-to-batch agronomic testing and downstream formulation safety.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • ISO 9001:2015 Quality Management – chemical raw material workflows
    • European Union Regulation (EC) 1107/2009 for plant protection product authorization
    • OECD Guidelines on the Testing of Chemicals (Relevant sections for intermediates)

    Typical usage ratio

    • Variable: 10–30% of initial molar feed in sulfonation, etherification, or carbamate formation stages
    • Final ratio adjusted depending on active moiety and desired selectivity profile

    Downstream process integration

    • Integrated early in aromatic ring functionalization for lead compound synthesis screens
    • Feeds into alkylation, amidation, or halogen-exchange steps for SAR (structure-activity relationship) optimization

    Final product types

    • New-generation herbicide AIs with pyridyl backbones
    • Systemic insecticide pre-cursors for protected crops
    • Marketed and pipeline fungicide compounds with enhanced photostability
    • Restricted-use active ingredient candidates for regulatory submission trials

    3. Advanced Electronic Material Precursors

    Electronics chemical manufacturers employ this compound to build fluorinated pyridine motifs for use in high-durability organic semiconductors and performance coatings. The precise placement of halogens enhances electron mobility and thermal stability in fabricated materials, supporting deposition and etching processes in display, OLED, and photovoltaic module production. Reliability in supply and trace impurity control remains key for thin-film material specification compliance.

    Industry compliance standards

    • IPC-5704 Cleanroom and Controlled Environments for Electronic Assemblies
    • RoHS Directive 2011/65/EU for hazardous substance limits
    • ISO 14001:2015 Environmental Management for electronics manufacturers
    • JEITA specification standards for display and semiconductor chemicals

    Typical usage ratio

    • Included at 5–15% by mass in proprietary precursor mixtures for functional layer synthesis
    • Content adjusted for dielectric constant targeting and thermal performance testing phases

    Downstream process integration

    • Introduced during solution-phase substrate preparation in OLED emission layer production
    • Participates in site-selective functionalization prior to vacuum evaporation, spin-coating, or inkjet-printing

    Final product types

    • Organic semiconducting materials for flexible displays
    • Photoactive coatings for advanced photovoltaic cells
    • Printed electronic components with stable thermal/electrical profiles
    • Specialty thin-film dielectrics for touch panels and wearable electronics

    4. Specialty Fine Chemical Synthesis for Dye and Pigment Manufacturing

    In specialty colorant production, dyestuff and pigment manufacturers adopt this chemical as a halogenated heterocycle intermediate, driving the formation of complex chromophores for textile, inkjet, and plastics sectors. The unique electronic properties imparted by the bromo, chloro, and fluoro substitutions determine lightfastness and spectral characteristics in the final pigment molecules. Formulators require high assay and minimal residual by-products to meet performance and regulatory colorant specifications.

    Industry compliance standards

    • REACH Regulation (EC) No 1907/2006 on chemical safety for imported/exported colorants
    • ISO 9001:2015 for specialty chemicals quality practices
    • Oeko-Tex Standard 100 certifications for textile dye safety (where used for fabric applications)
    • AP(89)1 Resolution guidelines for pigment use in plastics and toys (Council of Europe)

    Typical usage ratio

    • Ranges from 8–20% by mol in electrophilic aromatic substitution or cross-coupling syntheses
    • Optimized for chromophore intensity and UV stability in final dye or pigment formulation

    Downstream process integration

    • Enters in early halogenated intermediate build-up during multi-stage chromophore assembly
    • Included in controlled temperature and inert atmosphere couplings to restrict unwanted isomers

    Final product types

    • High-performance textile disperse dyes for polyester and acrylic fiber coloration
    • Special effect pigments for digital and security inks
    • UV-resistant color concentrates for automotive plastics and packaging films
    • Stable fluorescent dyes for analytical and biological imaging reagents
    Free Quote

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    Certification & Compliance
    More Introduction

    3-Bromo-2-Chloro-5-Fluoropyridine: Quality Built From Experience

    We have spent decades developing strong practical knowledge in halogenated heterocyclic building blocks, with a focus on ensuring every batch serves the chemists and process developers who rely on consistent, reproducible results. Among our portfolio, 3-Bromo-2-Chloro-5-Fluoropyridine stands out for unique features that allow synthetic chemists to push reaction boundaries, enabling precise control over regioselectivity in pharmaceutical intermediates, agrochemical candidates, and specialty materials. Its molecular arrangement, combining three distinct halogens on a pyridine ring, makes it a valued starting point for coupling reactions.

    Model, Consistency, And Process Know-How

    Customers often ask about crystallinity and moisture content because small differences in raw material handling create significant impacts during scale-up. Over time, we’ve learned that even after purification steps, trace moisture or residual solvents can threaten the reproducibility of Suzuki or Buchwald-Hartwig couplings. For this reason, we use batch-wise moisture controls and gas-tight packaging. Each lot of 3-Bromo-2-Chloro-5-Fluoropyridine undergoes purity verification by HPLC and GC, targeting a minimum purity of 98%. We report levels of potential cross-contaminants—mainly structurally related halopyridines down to low ppm. This approach lets us minimize downstream purification for customers, reducing waste and operational time.

    In routine usage, we’ve seen how this pyridine derivative’s precise substitution pattern offers selectivity that other similar compound classes don’t match. The combination of the bromo group at position 3 and the chloro group at position 2 blocks unwanted side products during palladium-catalyzed cross-coupling, while the fluorine at position 5 helps stabilize intermediates. That’s why medicinal chemists, particularly those working on kinase inhibitor scaffolds, value this compound as a core synthon.

    How Structure Drives Applications

    Compared with unsubstituted pyridine or mono- or di-halogenated analogs, 3-Bromo-2-Chloro-5-Fluoropyridine cuts down synthetic steps by offering orthogonal reactivity. Chemists aiming for stepwise functionalization can exploit the distinct leaving group capabilities—bromine for high-yield cross-coupling, chlorine for selective displacement under controlled conditions, and fluorine for later-stage fine-tuning. In our own scale-up projects, we have seen research partners cut project risk because this compound’s reactivity matches predictions, leading to less unanticipated byproduct formation and higher yields.

    Using this chemical in a long chain of transformations requires clarity on possible hydrolysis and halide exchange, so we provide detailed advice on solvent choices and reaction conditions from our process experience. For those engaged in combinatorial chemistry or library synthesis, we regularly support tonne-scale orders, delivering each lot with tight control of isomer and impurity profile. This compound’s role in forming nitrogen heterocycle frameworks or as a precursor for fluorinated pyridine derivatives means it serves a purpose from early-stage lead optimization through to commercial process routes.

    How Our Production Approach Makes A Difference

    Scaling halogenated pyridines is not a one-step procedure; there’s no shortcut when one’s aim is batch-to-batch reliability at hundreds of kilograms. We start from carefully controlled raw materials. Our chlorination, bromination, and fluorination operations include in-line monitoring with real-time analytics to catch deviations early. Operators sign off at every step, a process rooted in decades of experience with pyridine intermediates. During storage, we use desiccation and argon blanketing to halt hydrolysis, since even trace moisture can compromise downstream Suzuki reactions.

    Periodic feedback from end-users shapes our procedures. One research customer informed us of a trace side product impacting their downstream arylation step. Working closely with their analytical team, we adjusted purification to target that impurity specifically, resulting in cleaner material for their process and, ultimately, higher activity in their final pharmaceutical compound. That experience drove us to adopt extra quality checks for each synthesis stage.

    Key Differences From Other Pyridine Derivatives

    What separates 3-Bromo-2-Chloro-5-Fluoropyridine from compounds like 2,3,5-trichloropyridine or 5-bromo-2-chloropyridine boils down to how nucleophilic aromatic substitution unfolds. The three-halogen layout allows more predictable site-selectivity. For chemists seeking to avoid poly-substitution or scrambled halogen exchange under copper or palladium catalysis, this molecule’s electronics protect the core skeleton. Our NMR and LC-MS process controls catch even low-level rearrangement, making sure each shipment lines up with the precise structure clients expect.

    Other suppliers often overlook trace byproducts or oxidized material introduced during aggressive halogenation. Our facility’s closed-system synthesis and sequential halogen introduction reduce over-chlorination and other side reactions. We examine each lot for oxidative, hydrolytic, and thermal stability, an approach based directly on using these molecules in our own R&D labs before delivering them to customers.

    Usage Insights From Practical Chemistry

    In pharmaceutical discovery, 3-Bromo-2-Chloro-5-Fluoropyridine enters synthesis streams where speed and yield matter. Its trio of halogens lets chemists orchestrate multi-step transformations, converting each position selectively. In one collaborative project, a medicinal chemistry team applied sequential cross-coupling to replace first the bromine, then the chlorine, saving multiple protection/deprotection steps compared to using less-substituted pyridines. This meant fewer purification cycles and more time spent on valuable lead development.

    From an environmental perspective, our team dedicates effort to minimize halogenated waste. Our reactors recycle unreacted halogenating agents, and we neutralize effluents to align with both regional and global regulatory standards. In scale-ups for crop protection intermediates, customers repeatedly point to our certificate of analysis transparency, noting that tight impurity control helped pass not only lab trials but also regulatory filings. This reduces the risk of reruns or process setbacks on their end.

    Agrochemical innovators find this compound’s substitution pattern fits with accelerated lead optimization, especially in areas stressing higher metabolic stability and environmental breakdown. Our pilot plant routinely tunes the fluorination and bromination conditions to maintain the delicate balance needed for these applications. Clients come to us when they encounter difficulties with shelf-stability or reactivity drifts—areas where our history with moisture-sensitive reagents pays off.

    Lessons From Ongoing Collaboration

    We partner closely with downstream users and R&D teams. When unexpected reactivity or stability issues emerge, open dialogue allows solutions. In more than one case, we redesigned packaging and shipping protocols after learning that fluctuating transit conditions compromised certain custom formulations. Insights gained from these projects find their way back into batch process improvements, from more robust desiccation to trace metal screening for catalysts.

    Multiple customers requested analytical data packages tailored to regulatory dossiers, especially those engaged in API (Active Pharmaceutical Ingredient) route development. Satisfying that requirement guided us to build deeper analytical resources—ranging from polymorph analysis to elemental halide detection—and support customers not simply as suppliers but as partners invested in mutual regulatory success.

    How Our Values Shape Product Quality

    Commitment to consistent high grade doesn’t begin and end with batch testing. We draw on operator training, rigorous adherence to process schedules, and continual investments in automation to cut variance. Our lab team works closely with in-plant operators, monitoring each stage so deviations never go unexamined. This culture stems from years of serving chemists who demand certainty because unplanned changes upend expensive projects. Every process tweak stems from practical feedback—sometimes as small as a refinement in drying temperature or solvent grade, other times involving major updates to analytics or workflow.

    We believe that transparent communication with our clients underpins trust. Every certificate we send tells the whole story of the lot: what impurities we found and controlled, what method adjustments we made, and how each step traces back to our core values of reliability and continuous improvement.

    Meeting Industry Expectations And Beyond

    International customers expect not only purity but traceability, regulatory support, and clear documentation of all changes. Our quality system aligns with ISO standards for pharmaceutical ingredients and specialty intermediates. Analytical chemists can request additional test results because our team maintains both standard and customized reference spectra. Years spent working on cross-border supply chains taught us that delayed information can jeopardize entire shipments, so we prioritize clarity, traceability, and regulatory alignment.

    We’ve seen demand grow not just for the compound itself but for secure, consistent sourcing built on direct, honest relationships. Larger pharmaceutical and agrochemical companies often audit our facilities and validation records. They rely on evidence that we can trace each lot of 3-Bromo-2-Chloro-5-Fluoropyridine from raw material to final drum. The result is not only compliance but confidence for those developing new molecular entities or investigating higher-throughput library synthesis.

    Supporting Process Optimization For End Users

    Process chemists working with our team benefit from application support that comes out of real-life troubleshooting, not just technical papers. When a formula adjustment or downstream catalyst change is under consideration, our chemists share firsthand experience—identifying, for example, how trace water affects halogen exchange or how storage duration influences coupling efficiency.

    Such dialogue makes it practical for customers to get the results they expect, avoiding pitfalls that stem from silent changes in specification, packaging, or process protocols. Because we draw each improvement from hands-on experience and ongoing collaboration, feedback from synthetic chemists and process managers directly shapes how we evolve quality management and production practices.

    The Craft In Halogenated Pyridine Production

    With each run, our operators balance efficiency and care, mindful of the hazards and intricacies involved in halogenation. The team’s vigilance—across temperature, pressure, and reagent handling—matters as much as any automation. Years of accumulated process memory let us anticipate common bottlenecks, from crystallization rates to potential filter blockages, and make those practical decisions that keep batches within spec without guesswork.

    While many chemicals could theoretically stand in for 3-Bromo-2-Chloro-5-Fluoropyridine, few offer the same combinatorial of controlled reactivity, stability, and downstream flexibility. That’s one reason why research chemists and process engineers who encounter it for the first time so often adopt it as a cornerstone for further method development, from targeted library design to production-scale active ingredient synthesis.

    Practical Solutions To Common Challenges

    The specialty chemicals sector faces challenges that run from supply disruptions to increasingly stringent regulations. By focusing on direct production rather than trading or reselling, we retain control even when outside factors—such as logistics delays or feedstock fluctuations—pressure standard process flows. Holding raw material stocks on-site and maintaining full in-house analytics has let us navigate both COVID-era interruptions and international transport bottlenecks.

    For formulators and researchers on tight project timelines, a reliable supplier means they can focus on hitting their own innovation milestones rather than risk losing weeks to unexpected reprocessing. Open technical support lets us address unusual questions—from scaling solvent swaps between pilot and plant, to optimizing inert gas handling, to ensuring new products can be shipped with detailed regulatory documentation.

    Pushing Innovation While Maintaining Reliability

    Our plant investments center on two goals: product consistency and adaptive improvement. Staying close to customers, fielding requests for custom grades, alternate pack sizes, or enhanced impurity profiles, we apply modular process designs that permit adjustments without sacrificing throughput. Feedback on 3-Bromo-2-Chloro-5-Fluoropyridine frequently drives us to re-examine the fundamentals—whether a stage of purification can be improved or if alternate halogen sources provide a more sustainable end-to-end flow.

    We have reduced energy usage per batch by improving reaction heat management and adapted to stricter environmental compliance by reclaiming solvents at every stage feasible. Our operators use these opportunities to apply new skills and deepen chemical process competence, ensuring the entire value chain remains robust and future-ready.

    Partnering With Purpose

    Our focus remains steadfast: delivering 3-Bromo-2-Chloro-5-Fluoropyridine with attention to detail rooted in daily practice. With this approach, we support customers as they innovate in pharmaceuticals, agrochemicals, or new material development. Our technical and operational experience helps not only to deliver an often-demanding intermediate but also to work through the challenges and opportunities that come with using a multi-functional synthetic building block.

    This compound carries our reputation with every shipment, shaped by years of hands-on manufacturing, formulating, and problem solving. Whether used in a route for an exciting pharmaceutical lead, a robust crop protection agent, or an emerging specialty material, we approach every inquiry as a chance to share practical know-how and to get better—together with the research community.