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3-Bromo-4-Fluoropyridine

    • Product Name 3-Bromo-4-Fluoropyridine
    • Alias 3-Bromo-4-fluoropyridine
    • Einecs 857-306-5
    • 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
    VTB
    Specifications

    HS Code

    877658

    Chemical Name 3-Bromo-4-Fluoropyridine
    Cas Number 1072664-08-2
    Molecular Formula C5H3BrFN
    Molecular Weight 191.99 g/mol
    Appearance Colorless to pale yellow liquid
    Boiling Point 191-193°C
    Density 1.65 g/cm3
    Purity Typically >= 98%
    Smiles C1=CN=CC(=C1Br)F
    Inchi InChI=1S/C5H3BrFN/c6-4-1-2-8-3-5(4)7/h1-3H
    Refractive Index 1.565 (approximate)
    Storage Temperature 2-8°C
    Solubility Soluble in organic solvents (e.g., DMSO, chloroform)
    Flash Point 79°C

    As an accredited 3-Bromo-4-Fluoropyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 3-Bromo-4-Fluoropyridine is packaged in a 25g amber glass bottle with a tightly sealed cap, labeled with hazard warnings.
    Shipping 3-Bromo-4-Fluoropyridine is shipped in tightly sealed, chemical-resistant containers to prevent leaks and contamination. The package complies with all hazardous materials regulations, including appropriate labeling and cushioning. It is transported under ambient conditions and handled by trained personnel to ensure safety and maintain product integrity during transit.
    Storage Store **3-Bromo-4-Fluoropyridine** in a tightly sealed container in a cool, dry, and well-ventilated area, away from sources of ignition, heat, and moisture. Keep it away from incompatible materials such as strong oxidizing agents. Use appropriate personal protective equipment when handling and ensure storage in compliance with local regulations and safety guidelines for hazardous chemicals.
    Application of 3-Bromo-4-Fluoropyridine

    Applications of 3-Bromo-4-Fluoropyridine in Industrial Manufacturing

    3-Bromo-4-Fluoropyridine is a critical halogenated heterocycle for advanced chemical synthesis in regulated industries. As a primary producer, we supply large-scale manufacturers in sectors with clearly defined requirements and validated end uses. Below, we detail key downstream applications, reflecting real industry compliance, process protocols, use ratios, and final product outputs.

    1. Pharmaceutical Active Pharmaceutical Ingredient (API) Intermediates

    Innovator and generic pharmaceutical companies use 3-Bromo-4-Fluoropyridine in the synthesis of pyridine-based intermediates for targeted APIs such as kinase inhibitors, anticonvulsants, and anti-infectives. This halopyridine serves as a building block for constructing fluorinated and brominated functionalities, essential for pharmacological activity modulation. Its integration in multistep organic syntheses typically involves Buchwald-Hartwig, Suzuki, or nucleophilic substitution, customized during lead compound optimization or process scale-up.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • US FDA 21 CFR Part 210/211
    • EU EudraLex Volume 4 GMP standards
    • Relevant sections from United States Pharmacopeia (USP)

    Typical usage ratio

    • Generally 1.0–1.5 molar equivalents as a core reactant in stepwise synthesis of intermediates
    • Adjusted per target molecule's substitution and downstream yield

    Downstream process integration

    • First introduced during heteroaromatic coupling or halide exchange stages
    • Further processed via cross-coupling or nucleophilic aromatic substitution for advanced intermediates
    • Subjected to rigorous in-process controls (IPC) for residual halogen species

    Final product types

    • Small-molecule kinase inhibitors for oncology
    • Central nervous system actives (e.g., anticonvulsants)
    • Antiviral and antibacterial APIs

    2. Production of Agrochemical Active Compounds

    Manufacturers of crop protection agents employ 3-Bromo-4-Fluoropyridine to introduce specific halogenation patterns within fungicide and insecticide scaffolds. It becomes pivotal in ring formation and aromatic substitution for new-generation active ingredients with improved field stability and resistance management. Large-scale agrochemical synthesis utilizes this intermediate where electronic and structural attributes derived from the bromo and fluoro substituents enhance bioactivity.

    Industry compliance standards

    • FAO/WHO Good Manufacturing Practice for Pesticide Production
    • OECD GLP Principles for test item preparation
    • REACH (Registration, Evaluation, Authorisation and Restriction of Chemicals) for raw material traceability
    • Chemical Facility Anti-Terrorism Standards (CFATS) for precursor controls

    Typical usage ratio

    • Ranges from 0.5–2.0 molar equivalents depending on the active structure
    • Fine-tuned by downstream functionalization needs and yield targets

    Downstream process integration

    • Added in early-stage pyridine ring functionalization for scaffold assembly
    • Employed in palladium-catalyzed coupling to insert desired side chains
    • Undergoes purification by crystallization or flash chromatography prior to formulation

    Final product types

    • Triazole-based fungicides
    • Pyridine-derived insecticides
    • Herbicides featuring halopyridine cores

    3. Specialty Electronic Chemicals Synthesis

    Producers of organic electronic materials use 3-Bromo-4-Fluoropyridine to develop building blocks for OLED (organic light-emitting diode) and OFET (organic field-effect transistor) materials. The compound provides a synthetically versatile core for introducing electron-donating or -withdrawing groups, contributing to molecular engineering in semiconductors and functional coatings. Chemical engineers optimize batch and continuous processes for purity and reactivity, meeting the stringent demands of display and sensor industries.

    Industry compliance standards

    • International Electrotechnical Commission (IEC) 61249-2-21 for halogen content
    • IPC-4101 for base material specification sheets
    • RoHS Directive 2011/65/EU for hazardous substances
    • Internal QC specifications for purity and trace metals

    Typical usage ratio

    • Various: 1.0–2.0 molar equivalents based on desired substitution pattern
    • Batch size determined by final tonnage of electronic functional material

    Downstream process integration

    • First enters the process during small-molecule precursor synthesis for subsequent polymerization
    • Processed under inert atmosphere to prevent side reactions
    • Final purification to sub-ppm impurity levels required pre-polymerization

    Final product types

    • Pyridine-based host materials for OLED emissive layers
    • Organic semiconductors for transistors and sensors
    • Functional monomers for printed electronics

    4. Advanced Dye and Pigment Manufacture

    3-Bromo-4-Fluoropyridine serves dye producers formulating specialty colorants for textiles, inks, and high-performance coatings. The compound enables targeted halogenation in pyridyl dye structures, improving hue stability and fastness properties. Chemical development teams rely on batch-controlled introductions of halopyridine units to ensure uniform dye profile and meet regulatory colorant requirements for export markets.

    Industry compliance standards

    • REACH Annex XVII for dye ingredient restriction
    • Oeko-Tex Standard 100 for textile chemical safety
    • ISO 105 series for color fastness testing
    • ZDHC MRSL (Zero Discharge of Hazardous Chemicals) compliance for input chemicals

    Typical usage ratio

    • 0.2–1.2 molar equivalents depending on dye backbone substitution
    • Adjusted by target chromophore structure and shade depth

    Downstream process integration

    • Added during synthesis of pyridine functional intermediates
    • Used in subsequent coupling or condensation reactions for complex dye molecules
    • Careful control over residual halogen content during final product workup

    Final product types

    • Reactive dyes for cotton and blended textiles
    • Solvent dyes for plastics and inks
    • Specialty pigments for industrial coatings
    Free Quote

    Competitive 3-Bromo-4-Fluoropyridine prices that fit your budget—flexible terms and customized quotes for every order.

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    Certification & Compliance
    More Introduction

    3-Bromo-4-Fluoropyridine: Precision and Reliability for Advanced Synthesis

    Everything Begins with Quality Raw Materials

    Our years of hands-on production have shown that success in fine chemicals starts with the reliability of the base ingredients. 3-Bromo-4-Fluoropyridine marks a balance between demanding synthesis routes and those subtle tweaks in structure that chemists crave to open new possibilities. This compound, thanks to its unique bromine and fluorine substitution on the pyridine ring, gives organic synthesis chemists an edge when seeking both reactivity and selectivity.

    Specifications Reflect Purpose, Not Just Numbers

    We understand how frustrating it gets when a material’s specs don’t line up with real bench needs. Over the years, customer feedback has shaped our approach. Our 3-Bromo-4-Fluoropyridine typically comes at >99% purity after GC testing. We check for common contaminants like water, halide by-products, and residual pyridines, since side-reactions in sensitive coupling or cross-coupling routes can wipe out precious material. Small changes in impurity content can spell the difference between yield wins and wasted hours—so every lot we manufacture gets scrutinized batch by batch.

    Solubility in a range of common polar and non-polar organic solvents, plus carefully monitored melting and boiling points, allow for predictable behavior whether you’re running Suzuki, Buchwald-Hartwig, or other cross-coupling methods. Users working in medicinal chemistry, agrochemical intermediates, and material science often mention that our packaging and labeling have saved them confusion. Our labels always reference actual found values—never just “meets spec.”

    The Structural Edge: Why 3-Bromo-4-Fluoropyridine?

    We’ve handled a wide suite of halogenated pyridines. The unique pattern of a bromine at the 3-position and fluorine at the 4-position creates an electron distribution that stands out. That subtle push-pull effect between electron-withdrawing groups can accelerate some coupling reactions compared to more basic halopyridines such as 3-bromopyridine or 4-fluoropyridine used alone. In Suzuki couplings, for example, we’ve seen increased yields at milder conditions. Our own R&D staff ran pilot reactions, directly comparing this product to other mixed halopyridines, and found the activity profile attractive for quick ligand screening and rapid analog generation.

    That’s not simply an academic advantage. The difference plays out when scaling up, as better selectivity reduces clean-up needs, reduces solvent burdens, and cuts cycle time. We’ve helped chemists in several pharmaceutical settings build libraries faster by swapping in our 3-Bromo-4-Fluoropyridine—especially when other halogenated pyridines underperform.

    Batch Consistency Drives Trust

    Plain talk with chemists leads us to focus on control. From multi-kilo runs to smaller custom syntheses, we draw samples from every stage to verify composition and avoid batch drift. Handling sensitive reactions means chemists trust us only if our product does not surprise them with variable halide content, residual acids, or color changes. For every new batch, our QA team performs NMR, GC-MS, and titration checks, then archives reference spectra for transparency. We encourage partners to request analysis data—they see exact traces, not just numbers. It’s a habit we developed because we once spent too many nights troubleshooting unexplained reactivity, only to trace it back to trace contamination in the raw feeds.

    Applications Make Impact, Not Just Catalog Listings

    Users buy 3-Bromo-4-Fluoropyridine to synthesize pharmaceuticals, agrochemicals, and advanced materials—always chasing the new molecule, new property, or more efficient route. The precise location of the bromine and fluorine atoms, in our experience, lends itself well to stepwise functionalization. Medicinal chemists in particular rely on this motif when optimizing lead compounds for metabolic stability or binding selectivity.

    We’ve followed projects where our product led directly to kinase inhibitor scaffolds and modern herbicide candidates. The pyridine backbone travels intact through several steps, with the halogens offering distinct “handles” for modification. The advantage gained at these critical positions saves time, solvent, and resources throughout multi-step synthesis.

    What Sets This Compound Apart from Similar Products?

    We manufacture and supply a wide set of halogenated pyridines. Several chemists have noticed that the dual halogenation in 3-Bromo-4-Fluoropyridine offers tuning options that 3-bromopyridine or 4-fluoropyridine lack. Fluorine often sharpens metabolic stability and electron density, while bromine provides a go-to site for selective coupling. Compounds carrying both allow for nuanced stepwise transformations—not just one-off functionalizations.

    Our production experience tells us the seemingly simple modification of adding fluorine next to bromine can push downstream chemistry. Control over isotopic purity, low water content, and narrow distribution of by-products mean chemists can use this material straight from the jar in most high-throughput or automated settings. Instead of relying on external brokers who may blend or repackage, our direct control as manufacturers ensures single-origin material, fully traceable back to raw starting materials.

    We’ve learned from feedback that those working in automated polymer science or medicinal libraries require solubility in key solvents such as DMF, DMSO, THF, and toluene. By tuning our purification and drying steps, we deliver a free-flowing solid or liquid, depending on customer preference and batch size.

    Meeting Evolving Safety and Quality Standards

    Continuous improvement forms the backbone of our QA approach. Equipment upgrades allow for better containment, more efficient distillation, and improved purification. Regular audits—both our own and by clients—drive procedural discipline. We maintain strict records for every lot, including all reagents, batch numbers, and analytical reports. This data supports regulatory filings and customer due diligence. Over time, our approach to traceability has prevented costly recalls and helped customers speed up submissions for new chemical entities.

    Working directly with professionals on the front lines, we know patchy documentation or unexplained batch changes throw off development timelines. Our value comes from direct communication—users know exactly what changed, why, and how the adjustment improves the next run. We support thorough doc tracking rather than generic reassurance.

    Problem Solving as Core Value

    Chemical manufacturing rarely follows a perfect script. We remember entire years lost to improved yields, only to strike issues with drying, or months spent optimizing how the product crystalizes. Problem solving sits at the heart of how we work. If a solvent system in a downstream coupling fails due to unexpected solubility, our technical team can suggest alternative workups, or adapt drying conditions at the production stage. Chemists working with us appreciate the real-world troubleshooting and straight, detailed analysis.

    Quality improvement routines, such as shortening storage times for sensitive intermediates or using more robust drying agents, emerged from open discussions with our clients. When one pharma partner found that standard sealed drums let moisture in over time, our shift to high-barrier aluminum bags became standard, preventing later hydrolysis on storage. Small production tweaks, rather than one-size-fits-all solutions, lead to greater satisfaction all round.

    Improving Sustainability Through Design and Operation

    Sustainable practices are not simply marketing buzz. We buy raw materials directly from upstream producers, cutting multimodal shipping journeys that multiply emissions. Our plant runs at high conversion efficiency, recycling as much of the halide by-product as possible. Solvent choices—such as recycling THF or using lower toxicity workup systems—reflect the fact that we aim for real waste reduction, rather than only “compliance.”

    Reducing solvent use in purification and drying not only shrinks the carbon footprint but also lowers downstream burdens for customers. Dumping off solvent-heavy intermediates doesn’t line up with our approach: only finished, dry, and easily handled product leaves our plant. We prove this approach has cut waste in the past few years, and share these records with our clients if required.

    Direct Support for Production, R&D, and Scale Up

    Customers often bring their own synthesis challenges to the table. Some need a kilogram batch, others a pilot run for scale up, each with specific pressure on timelines and reproducibility. Our team listens closely, offering recommendations based not just on listed specs but also experience from hundreds of runs. A request for higher purity, improved flow properties, or tailored packaging has driven our incremental changes—such as shifting to larger crystal size for easier filtering or configuring our packaging for glovebox use.

    Responding to changing research needs, we offer single-lot and multi-lot blending for extra-large projects, keeping every incremental data point available to users. Several clients in pharmaceutical R&D have thanked us for providing in-depth impurity profiles, even on out-of-spec material, which helped prevent failed reactions or explained otherwise “mysterious” results on the bench.

    A Collaborative Approach, Not a Transaction

    We have never viewed ourselves simply as suppliers. Decades of experience reveal the best results come from close collaboration between the manufacturing floor and the research lab. Chemists approaching late-stage development can discuss their targets directly with our technical leads. Our team has supported custom route variation and even secondary purification, when a customer’s project required extreme conditions outside standard specs.

    Working side by side, we share process insight—such as how slow charging impacts the product’s color or how water removal timing sharpens the melting point range. Open channels mean faster learning for both sides, less guesswork, and more trust.

    Reliable Supply Chains—A Foundation in Ever-Changing Markets

    Market volatility in recent years has tested every supplier’s resilience. By directly managing our raw feedstocks, maintaining buffer stocks, and constantly inspecting supplier quality, we shield our customers from sudden gaps and variability. Periods of regulatory change or raw material shortages highlight the advantage of working with the source manufacturer rather than a middleman. Documentation, batch repeatability, and flexible delivery arise naturally from a supply chain managed directly by us.

    We’ve set up regular delivery schedules, managed customs issues, and prequalified logistics providers—always with the aim of minimizing downtime for the users. We communicate transparently about future supply, alerting partners to any changes. Our backup production lines assure delivery even during maintenance or upgrades.

    Investing in Future-Ready Chemistry

    We see ongoing investment in 3-Bromo-4-Fluoropyridine production as a crucial step for customers tackling increasingly complex molecules and tighter regulatory requirements. By investing in improved analytical instrumentation, automation, and cleaner energy, we strengthen both quality and capacity. These steps answer the growing demand for highly pure, low impurity pyridine derivatives, essential for drug development and materials innovation.

    Each advance in process brings new learning—such as better removal of trace colored by-products, sharper fractionation during distillation, or robust cooling for temperature-sensitive runs. Providing users with repeatable, “no surprises” material depends not only on skilled operators but also on continual upgrades.

    The Role of Detailed Feedback in Continual Improvement

    Nothing shapes production more than direct feedback from the bench. Our users have stopped batches, flagged odd colors, or sent notes on reaction performance. Every detail—whether a comment about needle-clogging, trace water, or just packaging fit—gets logged and analyzed. Several improvements stem from these close interactions. Chemists found that subtle variations in crystal morphology affected sample handling. By switching drying techniques, tweaking cooling rates, and separating finer fractions, our product now saves their time in weighing and dissolving.

    Our willingness to supply small or process-grade lots for parallel evaluation allows for rapid troubleshooting and fast turnarounds. If users notice shifts in their analytics, our team offers open-door access to trace records and full analytical profiles. This spirit of direct, mutual improvement defines our business model.

    Looking Ahead: Building on Experience, Not Hype

    The market for specialty halopyridines like 3-Bromo-4-Fluoropyridine is not crowded with hype but rather built on repeated success and learning from challenges. Working hand-in-hand with R&D and production labs worldwide, we see that predictable, high-purity product is non-negotiable for the latest pharmaceutical, agrochemical, and material projects. Reliability, detailed traceability, and direct support tip the balance for most users wrestling with tight deadlines and complex chemistry problems.

    We remain committed to producing this compound not as a catalog afterthought, but as a cornerstone ingredient developed and manufactured to help chemists innovate, troubleshoot, and ultimately succeed in building tomorrow’s molecular solutions.