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1,4-Dibromo-2-Fluorobenzene

    • Product Name 1,4-Dibromo-2-Fluorobenzene
    • Alias 1,4-Dibromo-2-fluorobenzene
    • Einecs 610-201-2
    • 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

    215587

    Cas Number 1435-54-1
    Molecular Formula C6H3Br2F
    Molecular Weight 253.90 g/mol
    Appearance Colorless to pale yellow liquid
    Boiling Point 226-228 °C
    Density 1.97 g/cm³ at 25 °C
    Refractive Index 1.610 at 20 °C
    Purity Typically ≥98%
    Solubility Insoluble in water, soluble in organic solvents

    As an accredited 1,4-Dibromo-2-Fluorobenzene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle, 100g, sealed with a screw cap, hazard labels, product name and CAS, manufacturer details, chemical purity specified.
    Shipping **Shipping Description:** 1,4-Dibromo-2-Fluorobenzene is shipped in tightly sealed containers, protected from light, heat, and moisture. It should be packaged according to hazardous chemical regulations, with proper labeling. Transport must comply with local, national, and international laws for hazardous materials to ensure safe delivery and prevent environmental contamination or human exposure.
    Storage 1,4-Dibromo-2-fluorobenzene should be stored in a tightly sealed container, in a cool, dry, well-ventilated area away from direct sunlight, heat sources, and incompatible substances such as strong oxidizers. Store it in a chemical fume hood if possible. Clearly label the container and keep it away from ignition sources, ensuring secondary containment to prevent leaks or spills.
    Application of 1,4-Dibromo-2-Fluorobenzene

    Applications of 1,4-Dibromo-2-Fluorobenzene in Industrial Manufacturing

    As a direct manufacturer of 1,4-dibromo-2-fluorobenzene, we supply to industries where this intermediate is crucial for advanced synthesis. Our product supports specialized downstream sectors across agrochemical active ingredients, pharmaceutical intermediates, colorants, and specialty polymers, adhering to strict quality and process standards at every stage of formulation.

    1. Crop Protection Active Ingredient Synthesis

    Producers of advanced agrochemical actives, particularly pre-emergent and post-emergent herbicides, rely on aromatic halogenated intermediates to introduce stable halogen atoms in key molecule frameworks. 1,4-dibromo-2-fluorobenzene enters during the core structure construction of specific pyridine and phenyl-based herbicides, offering reactivity that allows tight control over substitution patterns and enhancing field stability under varying soil humidity and pH conditions. Downstream facilities utilize rigorous in-process testing to ensure halogen purity profiles meet specifications set by global regulatory agencies.

    Industry compliance standards

    • OECD Guidelines for the Testing of Chemicals (Crop Protection)
    • FAO/WHO Maximum Residue Limits (MRLs)
    • China GB 2763 Pesticide Residue Standard
    • REACH Annex XVII (Agrochemicals)

    Typical usage ratio

    • 5–15% w/w of the target active synthesis batch, adjusted based on halogen substitution targets and scale-up kinetics

    Downstream process integration

    • Introduced during Grignard coupling or nucleophilic aromatic substitution as a core halogen source prior to final step functionalization

    Final product types

    • Phenyl-based herbicides (e.g., fluorobromide derivatives)
    • Pyridine herbicide actives
    • Halogenated intermediates for further crop protection molecule modification

    2. Pharmaceutical Intermediate for API Synthesis

    Innovative pharmaceutical producers use halogenated aromatics to synthesize intermediates for regulated drug substances, especially where ortho or para-disubstitution is critical to achieving activity and metabolic stability. 1,4-dibromo-2-fluorobenzene serves as a pivotal scaffold in select API supply chains, entering as a halogen donor in Suzuki-Miyaura, Buchwald, or Ullmann-type couplings. It empowers medicinal chemists to achieve stringent impurity profiles and supports reactions under cGMP conditions. Batch records ensure lot traceability and document retention toward European/US regulatory filings.

    Industry compliance standards

    • ICH Q7 GMP for Active Pharmaceutical Ingredients
    • US FDA 21 CFR Part 211
    • European Pharmacopoeia Monographs
    • Chinese Pharmacopoeia (ChP) intermediary controls

    Typical usage ratio

    • 2–8 mol% relative to coupling partners; varies with catalyst loading, step complexity, and final API yield targets

    Downstream process integration

    • Added in palladium- or copper-catalyzed cross-coupling as the core halogen donor, prior to cyclization or amination in API building block assembly

    Final product types

    • Fluorinated aromatic pharmaceutical intermediates
    • Target drug molecule precursors involving multi-halogen substituents
    • Registered starting materials for regulated API synthesis

    3. Electronic Chemicals—Organic Colorant and Dye Precursors

    Electronics and functional textiles manufacturers use halogen-substituted aromatics as selective precursors for specialty dyes, pigments, and liquid crystalline materials. In this environment, 1,4-dibromo-2-fluorobenzene introduces controlled halogen load during colorant backbone synthesis, where electronic delocalization and molar extinction coefficients dictate downstream performance. Strict raw material QC documentation and batch segregation ensure downstream colorant purity aligns with device or textile electronic requirements.

    Industry compliance standards

    • OEKO-TEX 100 for Eco-Friendly Textile Chemicals
    • ISO 9001:2015 for Quality Management Systems
    • RoHS Directive for restricted substances in electronic dyes
    • EN 71-3 migration limits (Toy Safety—colorants for inks)

    Typical usage ratio

    • 3–10% w/w as a colorant pre-synthesis input; concentration adapted for desired chromophore intensity and molecular orientation needs

    Downstream process integration

    • Reacted in aromatic nucleophilic substitution or metal-catalyzed coupling during pre-polymer colorant chain extension and pigment core construction

    Final product types

    • High-purity azo and anthraquinone dyes containing halogen functionalities
    • Photoresist intermediates for electronic displays
    • Halogenated pigment intermediates for LCD and OLED materials

    4. Specialty Polymer Monomer Synthesis

    Manufacturers of high-performance engineering plastics and specialty polymers select aromatic halogenated compounds as essential monomer precursors that drive polymer polarity and chemical resistance. In this context, 1,4-dibromo-2-fluorobenzene offers selectivity and thermal stability, especially valuable for functionalization of polyarylene and high-glass transition temperature materials. Strict input quality and process audit logs are maintained to ensure each monomer batch achieves consistent molecular weight distribution after polymerization.

    Industry compliance standards

    • ISO 14001 (Environmental Management Systems for Polymer Plants)
    • ASTM D4066 for plastics material classification
    • UL 94 flame classification (where applicable to polymers)
    • REACH SVHC reporting for monomer use

    Typical usage ratio

    • 1–7% by total monomer mass, with adjustments for targeted polymer backbone halogen load and co-monomer selection

    Downstream process integration

    • Incorporated during step-growth or chain-growth polymerizations, typically combined with functional dihalide or diamine co-monomers for backbone extension

    Final product types

    • Halogenated polyarylene ether-based engineering plastics
    • Specialty copolymers resistant to chemical degradation
    • High-performance plastics for automotive or electronic component casings
    Free Quote

    Competitive 1,4-Dibromo-2-Fluorobenzene prices that fit your budget—flexible terms and customized quotes for every order.

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    Certification & Compliance
    More Introduction

    1,4-Dibromo-2-Fluorobenzene: A Manufacturer’s Perspective

    Working With 1,4-Dibromo-2-Fluorobenzene in Chemical Synthesis

    Long before 1,4-dibromo-2-fluorobenzene made its way onto customer order sheets, our team spent years refining its synthesis and looking for ways to sharpen selectivity, improve purity, and keep up with the real challenges the industry faces. At our plant, every batch represents not only a chemical compound but also the lessons learned from years of feedback and the ambitions of researchers in pharmaceuticals, agrochemicals, and specialty material sectors.

    The identification number we use internally, sometimes called the model or referred to as its CAS 26237-42-5, simply helps with traceability, ensuring complete control from raw material onboarding to the final sealed drum. What matters most beyond numbers is performance—how the product holds up in real-world reactions, how it translates into higher yields, and how impurities can play havoc if ignored. Our team has found the physical consistency—crystalline powder, solid at room temperature—works best for weight accuracy and long-term stability. We standardize each lot to a purity above 98%, confirmed with GC and NMR analytics, because trace contaminants can cripple downstream catalysis. By keeping moisture and other halogenated side products out, we keep our customers’ synthesis as predictable as possible.

    Why This Halogenated Benzene Matters

    Anyone who works hands-on at the reactor bench knows how important halogenated intermediates are for cross-coupling chemistry. 1,4-dibromo-2-fluorobenzene sits in a special place among substituted benzenes due to its selective bromination pattern and the presence of fluorine. Compared to a straight 1,4-dibromobenzene, you’re adding a fluorine atom at the ortho position. That one atom makes a clear difference in both reactivity and the resulting molecular scaffold’s properties.

    The fluorine doesn’t just change the electron density; it steers the entire reaction course in Suzuki, Stille, or Ullmann-type couplings. We have customers building pharmaceutical scaffolds who praise how the compound’s dual bromides and strategic fluorination open doors that unsubstituted or mono-halogenated benzenes can’t. The ortho-fluorine increases selectivity and helps with site-specific activation, giving process chemists an edge when they want to introduce further heteroatoms or swap out the bromine in later steps. The products end up with improved bioavailability, binding strength, or simply more IP runway for complex projects.

    Real-World Challenges and Production Nuances

    Everyone outside the factory gate expects consistent performance, but as a producer, we know how many hurdles come with making and supporting 1,4-dibromo-2-fluorobenzene at scale. The classic halogen exchange and directed ortho-lithiation methods look straightforward on paper, but upscaling these requires careful handling of reagents, temperature control, and rigorous atmospheric safeguards. We have moved away from smaller glass reaction setups to jacketed, closed vessels lined with corrosion-resistant alloys—leak prevention and purity always come before squeezing out a few extra kilograms per shift.

    Another juggling act sits with purification. Early in our years, we dealt with brominated byproducts that traced back to issues with reagent dosing and stirring. Even small traces of tribrominated material or off-isomer formation create headaches for pharma clients, who face tough analytical scrutiny with regulatory filings. To dial this out, we now integrate inline NMR and advanced chromatography in the QC loop, which lets us intercept any out-of-spec lots before they hit the final line. These steps consume time and cost, but they are necessary. We’ve found it easier to adapt these technologies internally than keep answering complaint tickets upstream.

    How 1,4-Dibromo-2-Fluorobenzene Stands Out From Similar Intermediates

    Chemical manufacturing is about choices. Our product often shares the shelf with compounds like 1,4-dibromobenzene, 2-fluorobromobenzene, or even more heavily substituted benzenes. Chemists pick between them based on electronic effects, steric demands, and end-use ambitions. In the plant, these can look the same on a logistics invoice, but we see how small changes in structure force a different reality during production and application.

    Run-of-the-mill dibromobenzene has long stood up in carbon–carbon bond formation, but dropping a fluorine atom at the 2-position does more than tweak mass balance; it shifts the entire reactivity map. Fluorine, with a high electronegativity, lends itself to different activation, while the bromo groups provide sites for cross-coupling or nucleophilic aromatic substitution. These features mean our product grants medicinal chemists the freedom to stepwise build more complex molecules, reach targets with greater drop-in compatibility, and reduce the need for additional protecting group strategies. In electronic and materials arenas, this compound’s specific substitution enables properties like altered dielectric or improved molecular alignment within organic electronics, which our customers have reported as key for reliability and performance.

    Materials scientists also notice the difference in solid-state packing and melting points, which play a role in how well they can integrate the intermediate into more demanding polymers or coatings. Small-scale researchers often look past these aspects, but our bulk users rely on 1,4-dibromo-2-fluorobenzene’s specific profile to circumvent problems like unmanageable crystallization or excessive side reactions at higher scales. They are not just buying a reagent—they are investing in reduced risk and repeatable results.

    Managing Supply, Traceability, and Quality Pressure

    Markets have shifted dramatically in the last decade, both in volumes and in the level of documentation required. Preparing for an audit is normal, with questions flowing about the origins of bromine salts or the fluorobenzene precursors we use. We have responded by making our traceability sharper; each drum is mapped from lot tagging down to the rawest input. Without this control, we have seen how supply shocks or regulatory swings can choke the entire chain—anything short of full-documentation stops customers from keeping their own downstream processes compliant.

    We have also faced growing scrutiny from sustainability and occupational safety circles. Bromination reactions have always carried the stigma of hazardous reagent use and tough effluent control. We approached the challenge by updating to closed-loop waste treatment systems and switching to lower-emission solvents. Operating above mere compliance is not just a marketing point; it’s the only practical path if we want to maintain operations. We track regulators’ requirements closely and invest in both technical and staff training, rather than waiting for the next crisis to land.

    Responding to Application-Specific Needs

    In pharmaceutical research, end-users demand fine control over both the functional group placement and impurity profile. We have seen requests for tighter control of residual halides, and even for bespoke purifications or micro-scale lot splits. While these smaller-volume requests are not the most profitable in terms of plant throughput, we understand their necessity for research labs tackling new therapeutic candidates. The need to move from milligram sample to tens of kilograms for preclinical lots puts stress on our production pipeline in surprising ways—unexpected bottlenecks rarely show up in the spec sheet.

    Not all end-users tell us precisely what application awaits our product, but feedback comes back fast when something diverges from their process window. One customer developing a next-generation OLED material described how minor impurities, invisible to most detection, caused complete color shift failures in their displays. Armed with that information, we revalidated our crystallization temperature windows and narrowed our final product spec, catching issues upstream and tightening the relationship between bench and bulk. For agricultural research, researchers often comment on the product’s consistent bromination, which avoids batch-to-batch variability that could throw off efficacy or toxicity screens. These lessons travel through our own knowledge base, making the compound more robust.

    Continuous Improvement—A Core Producer’s Mindset

    Manufacturing a halogenated aromatic is not a one-and-done activity. The market keeps shifting. Techniques that worked five years ago lose ground to more refined demands and better analytic tools. We notice trends where users want higher-purity material, lower residual moisture, or changes to packaging that better meet EHS requirements. Responding means ongoing investment in pilot-scale upgrades and periodic technology swaps. We dedicate significant resources to updating both plant equipment and staff skill sets, allowing us to remain ahead of basic compliance and continue serving specialists in their fields.

    Globalization forced changes in how we view reliability. Shipments once considered routine now involve customs checks and longer lead times. Our planning systems have addressed this through safety stock and more local warehousing. We advise partners who purchase regularly to forecast at least a quarter out, ensuring stable supply and better pricing. Disruption in one area—be it energy price or regulatory clampdown—rarely stays local for long. We have learned to manage risk not just to preserve our own business, but to ensure our customers never face shortages that could throw off their own deadlines.

    Collaboration With End-Users—Lessons From the Field

    Our role doesn’t end at the point of sale. Feedback loops, successful or not, shape the future of any specialty intermediate. We frequently collaborate on technical troubleshooting when a process stalls or an unanticipated byproduct emerges. Sometimes, the answer involves a slight tailoring of the bromination step or introducing tighter post-reaction filtration for critical-phase products. For the electronics industry, our direct support on handling and storage practices has stopped performance drift for sensitive applications, where minute traces of air or light exposure matter.

    Open lines with application chemists and engineers accelerate issue resolution and product refinement. These conversations have taught us that written specs never tell the whole story; there is always nuance in actual processing environments. Sometimes, we have adapted drum lining materials or switched shipping partners to avoid temperature shocks, which preserved product quality from our gate right through to the user’s workbench. We see this as a shared responsibility—keeping our product true to the target molecule and its repeatable downstream performance.

    What Sets Production-Rooted Companies Apart

    A real manufacturer lives inside every detail of their chemistry, from sourcing raw bromine that meets both purity and sustainability standards to qualifying every analytical sequence and vetting every supply chain link twice. The trust end-users place in 1,4-dibromo-2-fluorobenzene—whether for multistep syntheses or next-generation device fabrication—rests on this diligence.

    Small failures pile up fast in this industry, and we have learned it’s better to over-invest in risk control than chase apologies after a recall or regulatory review. Having an in-house R&D team enables faster updates and real-time troubleshooting, translating to more reliable product for everyone, not just the loudest customer. Ongoing investments into greener and more efficient halogenation methods let us support users who face mounting compliance costs, often before they are forced to request specific documentation.

    Looking Ahead—Anticipating Industry Evolution

    Emerging research trends suggest that future demand for 1,4-dibromo-2-fluorobenzene will only expand, especially as medicinal and materials chemists drive deeper into fluorinated and poly-halogenated arenas. We see increased requests for technical consultation—everything from greener synthetic alternatives to batch traceability to support early-stage regulatory filings. As the science grows more complex, so does the need for transparency, speed, and accountability from manufacturers like us.

    Developing predictive inventory models helps prevent shortages. Engaging in pre-competitive conversation with standards-setting bodies helps smooth regulatory headwinds. Prioritizing these approaches allowed us to adapt ahead of many market shocks—and the capabilities we have built ensure both supply and expertise for even first-time users and established partners alike.

    Conclusion: Bringing Real Value To End-Users Through Manufacturing Expertise

    Every kilogram of 1,4-dibromo-2-fluorobenzene represents more than just a line on a reagent catalog. It’s the accumulation of decades of technical experience, a rigorous approach to purity and safety, and a deep respect for the unpredictable challenges that come with pushing chemical innovation forward. From our standpoint as a core producer, our work hinges on anticipating issues before they become problems, making ongoing investments in plant and people, and anchoring our operations in traceability and technical rigor.

    Our product will keep evolving as our clients do; we see every order as an opportunity to do better—for the application scientist, the process chemist, and ultimately, the communities served by end-use breakthroughs in pharmaceuticals, electronics, and specialized materials. The day-to-day reality inside a factory rarely makes headlines, but it shapes the results our customers rely on, molecule by molecule, shift after shift.