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2-Bromo-5-Fluoro-3-Picoline

    • Product Name 2-Bromo-5-Fluoro-3-Picoline
    • Alias 5-Fluoro-2-bromo-3-methylpyridine
    • Einecs 809-175-5
    • 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

    417910

    Product Name 2-Bromo-5-Fluoro-3-Picoline
    Cas Number 1050507-46-6
    Molecular Formula C6H5BrFN
    Molecular Weight 190.02
    Appearance Colorless to pale yellow liquid
    Boiling Point 170-172 °C at 760 mmHg
    Density 1.6 g/cm3
    Purity Typically ≥98%
    Solubility Slightly soluble in water; soluble in organic solvents
    Smiles CC1=C(N=CC(=C1Br)F)
    Synonyms 5-Fluoro-2-bromo-3-methylpyridine
    Refractive Index 1.55 (approximate)
    Storage Condition Store in a cool, dry, and well-ventilated place
    Hazard Statements Harmful if swallowed or inhaled

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

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    Application of 2-Bromo-5-Fluoro-3-Picoline

    Applications of 2-Bromo-5-Fluoro-3-Picoline in Industrial Manufacturing

    As an established manufacturer of 2-bromo-5-fluoro-3-picoline, we support demanding industrial partners by supplying high-purity intermediates for regulated sectors. Our advanced process management and traceability allow us to respond to precise requirements in downstream formulation, synthesis, and final product integration. The following application scenarios reflect major commercial uses of this chemical, driven by sector-specific compliance and real operational workflows.

    1. Agrochemical Intermediate for Select Herbicide Synthesis

    2-bromo-5-fluoro-3-picoline serves as a key halogenated building block in the synthesis of heterocyclic herbicidal actives, especially within pyrazole and pyridine-based classes. Downstream manufacturers integrate this intermediate at the core ring-substitution stage, using tightly controlled reaction conditions to ensure consistent coupling. Its purity directly impacts target product yields and is routinely monitored against residue thresholds due to its structural similarity to regulated environmental contaminants.

    Industry compliance standards

    • EU Regulation (EC) No 1107/2009 for Plant Protection Products
    • EPA 40 CFR Part 180—Tolerances and Exemptions for Pesticide Chemical Residues
    • ISO 9001 for production quality management
    • FAO/WHO technical guidelines for pesticide specification

    Typical usage ratio

    • 5–12% w/w of total reaction feed, with proportion adjusted for active ingredient targeted molecular weight

    Downstream process integration

    • Charged as a principal halogenated intermediate in the nucleophilic aromatic substitution or Suzuki coupling step
    • Introduced after base pyridine framework assembly, prior to final cyclization
    • Strict quality control enforced during addition to minimize formation of process impurities

    Final product types

    • Selective pre- and post-emergence herbicide actives (e.g., for cereal and oilseed crops)
    • Registered active ingredients for branded and generic herbicide formulations
    • Co-formulated concentrate for direct field application
    • Water-dispersible granules and suspension concentrates for agricultural use

    2. Pharmaceutical Intermediate in Antiviral Drug Synthesis

    This compound acts as a core pyridine fragment in the synthesis pathway of certain antiviral drug candidates, particularly in nucleoside analog development and the assembly of small-molecule kinase inhibitors. Its position-specific halogenation enables targeted functionalization, which supports further elaboration through reductive amination, Suzuki, or Sonogashira couplings. GMP documentation is maintained from batch to batch, and trace-level impurities are documented to support regulatory filings.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP/NF and Ph. Eur. guidelines pertaining to starting materials
    • 21 CFR Part 211 – US FDA cGMP for finished pharmaceuticals
    • Certificate of Suitability (CEP) requirements for EU submissions

    Typical usage ratio

    • 3–7% mol/mol relative to total reactants, tuning for batch size and downstream step requirements

    Downstream process integration

    • Introduced at the functionalized pyridine assembly step, prior to amide coupling or alkynylation
    • Handled in enclosed reactors to minimize cross-contamination
    • Residual level verification at in-process QC checkpoints

    Final product types

    • API intermediates for investigational antiviral compounds
    • Small-molecule drugs in clinical or pilot production
    • Advanced building blocks for kinase inhibitor pharmaceutical pipelines
    • Regulatory reference standards for process validation

    3. Advanced Material Precursor in Electronic Chemicals

    2-bromo-5-fluoro-3-picoline finds application as a key functional group donor in the production of specialty organic electronics materials, including precursors for high-performance liquid crystal and OLED emitters. Its substitution pattern enables downstream fine-tuning of photophysical properties essential for uniform alignment and emission efficiency. Downstream manufacturers implement rigorous analysis to confirm lot-to-lot consistency, as device yield depends heavily on chemical uniformity and absence of trace metals or halide byproducts.

    Industry compliance standards

    • RoHS (Restriction of Hazardous Substances) Directive 2011/65/EU compliance
    • REACH Regulation (EC) No 1907/2006 for chemical safety
    • JEITA and SEMI standards for supply chain quality
    • ISO 14001 for environmental management in electronics manufacturing

    Typical usage ratio

    • 1–4% by weight within precursor solution, adjusted according to designed functional group density in oligomer or polymer matrix

    Downstream process integration

    • Incorporated at core ring-masking step of monomer preparation via Pd-catalyzed aryl-amination or C–C coupling
    • Quality verified prior to admixing with substrate-specific ligands for light-emitting layers
    • Managed in cleanroom conditions to meet electronic material standards

    Final product types

    • OLED small molecule emitters (blue and green channel dominant)
    • High-contrast liquid crystal alignment layers
    • Intermediates for organic photovoltaic active layers
    • Patterned films for flexible display manufacturing

    4. Chemical Building Block in Specialty Dye & Pigment Synthesis

    This halogenated picoline derivative offers a unique substitution pattern leveraged in designing specialty dyes and pigments for industrial coloration, including fluorogenic and halogenated pigment systems used in security inks or high-durability coatings. Controlled addition allows precise adjustment of hue, lightfastness, and resistance to oxidative fading. Downstream manufacturers require documented analysis confirming trace impurity levels and compliance with dye industry regulatory bodies.

    Industry compliance standards

    • REACH and CLP regulation compliance for industrial dyes
    • ETAD (Ecological and Toxicological Association of Dyes and Organic Pigments Manufacturers) guidelines
    • CEN EN 71-3 for heavy metal content in colored materials
    • ISO 105-B02: Color fastness to light in textile applications

    Typical usage ratio

    • 2–6% of reaction mass, raised or reduced based on required chromophore density and pigment batch scale

    Downstream process integration

    • Charged during stagewise diazotization or halogenation for nitro- or azo-dye synthesis
    • Utilized in the coupling of donor–acceptor pigment frameworks
    • Batch-tested for absence of prohibited halogenated byproducts

    Final product types

    • Fluorinated organic pigments for security printing
    • Industrial dyes for solvent-based inkjet systems
    • Halogenated colorants for automotive or aerospace coatings
    • Specialized textile and synthetic fiber dyes
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    Certification & Compliance
    More Introduction

    Spotlight on 2-Bromo-5-Fluoro-3-Picoline: A Versatile Compound for Modern Synthesis

    Walk into any well-equipped synthetic chemistry lab, and chances are you’ll spot shelves lined with specialty compounds, each telling its own story. Among these, 2-Bromo-5-Fluoro-3-Picoline stands out for people who work in developing new pharmaceuticals, advanced materials, and fine chemicals. This niche chemical might not capture headlines like lithium or silicon, but its impact echoes quietly in the background of innovation.

    What Sets 2-Bromo-5-Fluoro-3-Picoline Apart

    2-Bromo-5-Fluoro-3-Picoline offers a unique set of properties. Structurally, it features a pyridine ring with bromine and fluorine at distinct positions, setting up an interaction point for a range of synthetic applications. This specific arrangement opens doors for chemists to build more complex molecules without battling the reactivity and selectivity issues that crop up with less tailored building blocks.

    Many standard bromopyridines or fluoropyridines in the lab stash don’t deliver the same precise control over where chemical changes take place. That matters when trialing advanced reactions, especially in small-scale medicinal chemistry projects where cost and time carry real weight. Synthetic routes for bioactive molecules often run into dead ends with more generic halopyridines, causing wasted effort or impure results. Using 2-Bromo-5-Fluoro-3-Picoline, researchers can count on reactivity at the bromine site and fine-tune electronic effects via the fluorine—giving them levers for selectivity that make tough targets more accessible.

    Model, Purity, and Quality that Drive Results

    The batch-to-batch purity of 2-Bromo-5-Fluoro-3-Picoline influences the reliability of research outcomes. Impurities from hastily synthesized chemicals can send a project off in the wrong direction, especially when dealing with ultra-low residue limits or tight regulatory standards. A lot of specialty chemical vendors tout high-assay ratings—sometimes above 98% for this kind of product—which can look like a small difference on paper but proves crucial where side-products or minute contaminants might derail a synthetic pathway.

    In my experience working alongside medicinal chemists, having a dependable supply of high-purity building blocks takes some stress off a project timeline. The frustrations when a reaction fails due to mysterious, low-level contamination add up over time. Sticking with products that deliver reproducibly clean results lets chemists focus on exploration and problem solving, not endless troubleshooting.

    Usage Scenarios: Paving the Way for Breakthroughs

    Given its unique atomic arrangement, 2-Bromo-5-Fluoro-3-Picoline steps into the spotlight for projects that demand precision. People rely on it in stepwise coupling reactions, such as Suzuki-Miyaura or Buchwald-Hartwig cross-couplings, where the bromine acts as a leaving group. In these reactions, the fluorine atom helps modulate the electronic landscape, often resulting in better yields or easier purification compared to more generic analogues.

    Take the field of medicinal chemistry as an example. Drug discovery hinges on structural diversity, and even small shifts in the location or identity of functional groups can tip the scales between a hit compound and another forgotten candidate. The combination of halides on the pyridine ring lets researchers introduce new functional groups in a controlled fashion. I’ve seen teams transform 2-Bromo-5-Fluoro-3-Picoline into a range of intermediates, using it as a springboard to novel kinase inhibitors and anti-infective agents.

    Material scientists also benefit from the dual-halide pattern, especially when crafting ligands for metal-organic frameworks or developing small molecules for organic electronics. Dropping in a 2-bromo, 5-fluoro pattern brings subtle shifts in reactivity and solubility, which can be key to tailoring properties like charge transport or thermal stability. Trying to achieve the same with single-halogenated picolines usually leaves gaps in performance or bottlenecks in scalability.

    Differences that Matter: Comparing with Other Building Blocks

    Chemists always keep an eye out for differences that can tilt a reaction in their favor. It’s tempting to use whatever halopyridine is close at hand, but 2-Bromo-5-Fluoro-3-Picoline creates a distinct set of opportunities. Regular 2-Bromopicoline doesn’t deliver the same range of control due to the lack of fluorine’s electron-withdrawing influence. On the flipside, standard 5-Fluoropicoline misses out on the power of the bromine atom as a flexible handle for substitution.

    No one likes spending hours tweaking conditions only to end up with low yields or impurity issues. Tools like 2-Bromo-5-Fluoro-3-Picoline streamline synthesis steps: the bromine offers a gateway to arylation, amination, or carbon-carbon bond formation, while the fluorine’s presence can nudge reactivity in favor of products that are otherwise hard to isolate. Pieces like this make it feasible to chase more ambitious molecular structures without rolling the dice on unpredictable chemistry.

    Cost can be a concern, given extra synthetic steps needed to secure both halogen atoms in the right spots, but for high-value targets or projects where time carries a premium, this expense often pays for itself. Researchers who have spent afternoons separating inseparable isomers or purifying low-yield side products know the price of false economy in chemical acquisition.

    Real-World Challenges in Production and Application

    It’s easy to overlook what it takes to get pure specialty chemicals to the bench. Each batch of 2-Bromo-5-Fluoro-3-Picoline needs careful oversight, starting from precursor sourcing through final purification. Not every vendor takes the trouble to check for trace contaminants that might show up only at sub-ppm levels yet could ruin a late-stage drug candidate. Chemists who've dealt with regulatory filings or tough bioassays know a reliable supplier makes all the difference.

    In an ideal world, specialty chemical production would be fast, flexible, and eco-friendly. In practice, the synthesis routes for fluorinated aromatics involve hazardous reagents and generate more waste streams than most end users realize. Environmental footprints begin where synthesis does, not only at the point of use. Companies aiming for sustainable chemistry need to keep pushing for cleaner, safer synthetic routes and advocating transparent audit trails—think greener solvents, better waste management, reduced reliance on toxic reagents.

    Researchers increasingly ask about supply chain track records and batch testing, not just price and shipping dates. Knowing that a barrel's contents match the COA’s promises and that trace impurity profiles are characterized—these give teams confidence to scale up innovations and submit regulatory documents without fear of backtracking due to unseen chemical ghosts.

    The Value of Tailored Intermediates in Drug Discovery

    Medicinal chemists tend to be practical people, but their ambitions run high when the right tools are available. 2-Bromo-5-Fluoro-3-Picoline brings several advantages when building diverse heterocyclic libraries. The dual-halogen pattern allows for rapid diversification, something screens for new lead compounds demand. Single-halide picolines force extra synthetic manipulations, dragging timelines and sometimes leaving behind impurities difficult to separate.

    In my own work and discussions with colleagues, using hybrid-substituted building blocks has sped lead optimization projects, letting teams explore more chemical space before early preclinical cutoffs. Speed counts in competitive environments, and shaving even a week off a multi-step synthesis can ripple downstream—new compounds get into animal models sooner, keeping programs on track and under budget.

    Regulatory pressures also shape choices in building blocks. Compounds bearing both bromine and fluorine can sometimes offer lower off-target activity or clearer metabolic breakdown in vivo—advantages that aren’t always obvious from a desk chair. Studies have shown that small shifts in substituent patterns affect both binding affinity and pharmacokinetic properties. The ability to make substitutions efficiently, without introducing problematic residues, can mean the difference between progression and project closure.

    Risks and Safety Considerations in Scale-Up

    There’s a familiar tension between discovery and development in chemistry. Researchers get excited by novel structures, yet the demands plug in quickly once a process looks promising. 2-Bromo-5-Fluoro-3-Picoline has its quirks in handling: the presence of both a bromine and a fluorine atom gives rise to volatility or reactivity issues in certain conditions. Good ventilation and PPE are routine, but scale-up brings new risks—both to workers and the environment.

    Experienced plant chemists keep a close eye on thermal decomposition points and reactivity with common metals. Several anecdotal reports mention decomposition products at higher temperatures or in contact with base, likely leading to off-gassing. Training and robust handling protocols matter, particularly during distillation or purification—improper controls can vent halogenated vapors with health and environmental repercussions.

    On the safety side, stringent process guidelines and routine monitoring can head off most dangers. Many modern labs use real-time gas detection and secondary containment to keep halogen exposure negligible. At the end of its life cycle, waste treatment needs to neutralize both organic solvents and halide byproducts effectively. Regulations for handling waste streams from brominated or fluorinated aromatics continue to tighten worldwide. Partnering with disposal services that specialize in such materials removes a variable from the risk equation, letting chemists focus on the molecules themselves.

    Exploring Alternatives: Should Labs Rely on 2-Bromo-5-Fluoro-3-Picoline?

    There’s no single right answer for every project. Sometimes, labs do just fine with more basic halopyridines, especially early in route scouting. For advanced applications—where precision, purity, and efficiency drive decision-making—specialty building blocks outperform their cheaper, broadly available cousins. The payoff comes in less rework, fewer purification steps, and the ability to reach difficult substitution patterns without a gauntlet of optimization.

    Choosing the right intermediate often balances convenience against future flexibility. Projects chasing novel chemical space or aiming for regulatory approval in sensitive fields like medicine or electronics depend on clean, well-characterized materials as a baseline. In global collaborations, reproducibility and traceability can matter just as much as cost. Labs that invest in better starting materials often see reduced long-term costs through fewer delays and product recalls.

    For companies striving to stand out in the crowded pharmaceutical or electronics market, meeting internal and external quality standards isn’t just box-checking. Brand reputation hinges on the reliability of every intermediate—failures at late stages, or product recalls due to impurity profiles inconsistent with stated values, can wipe out years of effort. 2-Bromo-5-Fluoro-3-Picoline, by plugging gaps that generic alternatives can’t fill, becomes a quiet lever for risk mitigation and innovation acceleration.

    What the Future Holds for Specialist Building Blocks

    Demand for tailored chemicals looks set to grow as the pace of innovation climbs. Data from industry tracks indicate a rise in requests for multi-functionalized pyridines and other heteroarenes within pharmaceutical pipelines. Supply will need to keep up—not just in quantity but in quality and sustainability. Pressure for cleaner, greener processes grows every year, and companies slow to adapt risk dropping behind both in compliance and market share.

    Synthetic chemists who used to specialize in large, commodity chemicals increasingly delve into fine-tuning microbatches, supporting rapid prototyping in pharma, materials science, and digital electronics. The rise of flow chemistry and microreactor technologies hints at more nimble ways of creating complex intermediates like 2-Bromo-5-Fluoro-3-Picoline, reducing waste and energy consumption. In the past, custom chemistries seemed slow and expensive, but technological shifts make niche production both accessible and scalable.

    Younger generations entering the sciences will expect—and demand—full transparency regarding raw materials: where they come from, how they’re produced, and what their footprints look like. Bridging the gap between high-tech laboratory needs and responsible stewardship of chemical resources shows up not just in grant language, but increasingly in procurement decisions. Making informed choices about such compounds supports not just present-day discovery but the reputation and viability of research organizations long term.

    Putting It All Together: The Real Value of 2-Bromo-5-Fluoro-3-Picoline

    At the end of the day, having access to a toolkit that includes specialty compounds like 2-Bromo-5-Fluoro-3-Picoline lets chemists push boundaries. Single substitutions won’t always deliver the breadth of reactivity needed for cutting-edge work. Dual-functionalized intermediates grant flexibility, precision, and a pathway to cleaner, faster synthesis—whether the goal is a new medicine, an improved electronics material, or an exploratory piece of fundamental research.

    Chemistry rewards those willing to experiment and adapt. In a competitive field, overlooked intermediates can become the key to a breakthrough or a new line of products. While cost, sourcing, and environmental impact raise continued challenges, solutions rooted in careful supplier selection and attention to process details minimize risk. For some, these efforts might seem incremental, but over years, they build a foundation of reliability and respect.

    For research teams seeking a competitive edge, investing in purposeful, well-characterized building blocks opens doors to targets that might otherwise be out of reach. 2-Bromo-5-Fluoro-3-Picoline commands attention not just for its unique structure, but for its ability to turn stubborn chemical dreams into real, tangible results. Like many behind-the-scenes advances, it helps forge the path to new discoveries—one well-built molecule at a time.