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4-Bromo-2,6-Difluoroiodobenzene

    • Product Name 4-Bromo-2,6-Difluoroiodobenzene
    • Alias 1-Bromo-3,5-difluoro-4-iodobenzene
    • Einecs 840-175-5
    • 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

    599732

    Productname 4-Bromo-2,6-Difluoroiodobenzene
    Casnumber 885276-40-8
    Molecularformula C6H2BrF2I
    Molecularweight 331.89 g/mol
    Appearance White to off-white solid
    Purity Typically ≥97%
    Solubility Insoluble in water; soluble in organic solvents
    Smiles C1=C(C=C(C(=C1F)Br)F)I
    Inchi InChI=1S/C6H2BrF2I/c7-3-1-4(8)6(10)5(9)2-3/h1-2H
    Synonyms 4-Bromo-2,6-difluoro-1-iodobenzene
    Storage Store in a cool, dry, well-ventilated place

    As an accredited 4-Bromo-2,6-Difluoroiodobenzene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle containing 5 grams of 4-Bromo-2,6-Difluoroiodobenzene, sealed with a screw cap and hazard labeling.
    Shipping 4-Bromo-2,6-Difluoroiodobenzene is shipped in tightly sealed containers, protected from light and moisture. As a hazardous chemical, it is handled per relevant transport regulations (such as DOT, IATA, or IMDG) and may require labeling for toxic and environmentally hazardous substances. Transport should only be conducted by authorized carriers.
    Storage 4-Bromo-2,6-Difluoroiodobenzene should be stored in a cool, dry, well-ventilated area away from incompatible substances such as strong oxidizers and bases. Keep the container tightly closed and protected from light and moisture. Store at room temperature, preferably below 25°C. Use appropriate safety measures, including proper labeling and containment to avoid spills, contamination, or accidental exposure.
    Application of 4-Bromo-2,6-Difluoroiodobenzene

    Applications of 4-Bromo-2,6-Difluoroiodobenzene in Industrial Manufacturing

    4-Bromo-2,6-Difluoroiodobenzene supports specialized synthesis in advanced chemical industries. Our production aligns with the rigorous requirements of global manufacturers in pharmaceuticals, crop protection, specialty polymers, OLED intermediates, and fine chemical research. The following sections introduce major downstream segments using our product in specific, documented processes.

    1. Pharmaceutical API Intermediate Synthesis

    Pharmaceutical manufacturers employ this compound as a halogenated aromatic building block during the multi-step synthesis of active pharmaceutical ingredients, primarily within small-molecule pipeline research targeting kinase inhibitors and anti-viral agents. Its dual halogenation enables unique cross-coupling and nucleophilic substitution protocols essential for accessing fluorinated pharmaceutical intermediates. Reaction parameters typically favor Suzuki-Miyaura or Buchwald–Hartwig couplings under controlled temperature and pressure. Product integration directly affects the formation of C–C or C–N bonds in regulated API process streams.

    Industry compliance standards

    • ICH Q7 GMP for Active Pharmaceutical Ingredients
    • US FDA 21 CFR Part 211
    • EU EudraLex Volume 4 (Good Manufacturing Practice for APIs)
    • Ph. Eur. harmonization for starting materials (where applicable)

    Typical usage ratio

    • Applied at 0.75–1.30 molar equivalents relative to core fragments; ratio tuned to reaction excess and conversion rates specific to each target intermediate

    Downstream process integration

    • Integrated at the aryl coupling stage in route development, before core late-stage modifications, during the installation of pharmacophore moieties

    Final product types

    • Small-molecule kinase inhibitors (e.g., investigational oncology drugs)
    • Fluorinated anti-viral agents
    • Precursor intermediates for research-grade APIs
    • Pilot-scale pharmaceutical candidate compounds

    2. Agrochemical Intermediate Production

    Crop protection formulators use this compound as a key aromatic precursor in the manufacture of next-generation herbicides and fungicides, owing to its difluoro-substitution patterns that enhance bioactivity and metabolic stability. Application frequently involves selective halide exchange and metal-catalyzed cross-coupling to build fluorinated benzene scaffolds found in certain registered agrochemicals. Formulators rely on the consistent purity for critical steps in scale-up and pilot plant operations, targeting precision in downstream structure-activity optimization and field performance assessment.

    Industry compliance standards

    • FAO/WHO Guidelines on pesticide formulation quality control
    • ISO 9001:2015 for chemical synthesis quality management
    • REACH Annex VII safety requirements (Europe)
    • EPA TSCA Title VI reporting obligations (USA)

    Typical usage ratio

    • Usually 1.05–1.10 mol equivalents per coupling partner; ratio adjusted for process yield optimization and downstream purification ease

    Downstream process integration

    • Introduced at key aromatic derivatization stage, preceding formulation into emulsifiable concentrates or wettable powders for field use

    Final product types

    • Precursor to fluorinated herbicides (e.g., substituted phenoxy herbicides)
    • Intermediate for triazole or strobilurin-based fungicides
    • Synthesis blocks for insecticide R&D targets
    • Reference standards in agrochemical registration dossiers

    3. Specialty Polymer Monomer Sourcing

    Polymer chemists source our halogenated aromatic for the design of high-performance specialty polymers, particularly where controlled fluorination enhances thermal or chemical resistance in end-use plastics. The material enters nucleophilic aromatic substitution reactions or polycondensation steps to build monomers such as poly(arylene ether) derivatives. Its purity supports predictable reactivity in pilot polymerization and scale-up, achieving key physical properties in engineered materials for electronic or automotive sectors.

    Industry compliance standards

    • ASTM D5630 melt processing requirements for specialty polymers
    • ISO 9001:2015 polymerization QC controls
    • RoHS (Restriction of Hazardous Substances Directive) for downstream electronics
    • REACH registration of monomers (EU Regulation (EC) No 1907/2006)

    Typical usage ratio

    • Used at a feed concentration of 0.5–2.0% by weight, determined by desired fluorine incorporation and required polymer backbone substitution density

    Downstream process integration

    • Added at the monomer synthesis stage before controlled polymerization or polycondensation, feeding into extrusion or casting operations

    Final product types

    • Fluorinated poly(arylene ether)s and copolymers
    • High-performance engineering plastics for automotive or aerospace
    • Thermal-stable encapsulation polymers for electronic circuitry
    • Membrane materials for specialty filtration applications

    4. OLED and Display Material Development

    Display technology companies select this halogenated benzene for its role in synthesizing functional small molecules and intermediates incorporated into OLED (organic light-emitting diode) materials. Synthetic chemists rely on this compound for stepwise construction of electron-transport or hole-transport layers via Pd-catalyzed cross-couplings, leveraging its unique electronic profile to tailor charge balance and emission lifetime. Materials R&D teams closely monitor structure–property relationships that influence brightness and device reliability.

    Industry compliance standards

    • IEC 62321 (determination of certain substances in electrical and electronic products)
    • Control of Substances Hazardous to Health Regulations 2002 (COSHH UK)
    • ISO/IEC 17025-accredited laboratory testing for OLED compounds
    • Customer-specific NTD (Non-Toxicity Declaration) and purity specification requests

    Typical usage ratio

    • Supplied at 0.8–1.4 mol equivalent per coupling fragment; process chemists optimize ratio according to each display panel’s electronic requirements

    Downstream process integration

    • Employed in the fine chemical synthesis phase, as an aromatic precursor feeding into multi-step OLED or organic semiconductor intermediates production, prior to device fabrication

    Final product types

    • Electron-transport layer precursors
    • Hole-transport layer intermediates
    • Small-molecule OLED emitters
    • Advanced organic semiconductors for display backplanes

    5. Fine Chemical and Custom Synthesis Contract Manufacturing

    Research organizations and custom synthesis firms contract our facility for targeted supply of this compound as a modifiable aromatic core for the development of new compounds, analytical standards, and reference materials. Versatile reactivity supports a spectrum of halogen exchange, metalation, and cross-coupling protocols, serving leading-edge applications in method development and validation for regulatory reference or specialized material science projects.

    Industry compliance standards

    • ISO 17034 Reference Material Producer requirements
    • GLP (Good Laboratory Practice) OECD Principles
    • Client-specific material safety and data documentation
    • Chain-of-custody and traceability per ISO 9001

    Typical usage ratio

    • Used as received or at predetermined stoichiometric quantities, ranging from 0.2 to 2.0 equivalents depending on the scope of synthesis and target molecule architecture

    Downstream process integration

    • Integrated within fine chemical laboratories during early-stage development, high-throughput screening, or in analytical chemistry for identity and impurity profiling

    Final product types

    • Analytical reference standards
    • Custom intermediates for chemical screening libraries
    • Labeled compounds for research applications
    • Specialty reagents for surface science chemistry
    Free Quote

    Competitive 4-Bromo-2,6-Difluoroiodobenzene prices that fit your budget—flexible terms and customized quotes for every order.

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    Certification & Compliance
    More Introduction

    4-Bromo-2,6-Difluoroiodobenzene: An Authentic Manufacturer’s Perspective

    Complex Substitution for Precise Synthesis

    In chemical synthesis, few intermediates carry the directness and purpose found in 4-Bromo-2,6-Difluoroiodobenzene. We produce this compound directly at our facility with an emphasis on purity, careful handling, and reproducible quality. Its molecular structure, which brings together bromine, fluorine, and iodine substituents on a benzene ring, reflects considerable intent—a design that supports specific demands in pharmaceutical development, material science, and advanced organic chemistry. Over the years, our production teams have focused on refining the halogenation process, ensuring not only high assay material but controlled batch consistency. This attention to process details distinguishes us from the experience offered by traders who only relay information without a direct hand in the day-to-day management of chemical synthesis.

    Specifications—Not Just Numbers

    Laboratory and pilot-scale chemists often ask us whether our 4-Bromo-2,6-Difluoroiodobenzene reaches the minimum typical purity above 98%. Most find these figures reassuring, but the real value comes during post-synthetic analysis. Product retain samples consistently show tight control over residual solvents and minor isomer content, reflecting the stability of our reaction conditions and purification path. The melting point and NMR spectra repeat with remarkable reliability; technicians new to our plant frequently note this steadiness as a mark of skilled production.

    The product comes as an off-white to light beige crystalline solid. Pack sizes start at grams for research projects and build up to multi-kilogram batches for process development. By overseeing each stage—from the first halogen exchange to final packaging—we know that no step is left to chance. We never treat standardization as an afterthought. Customers purchase the same quality compound whether the order is small or large, and that consistency makes scaling chemical processes far more predictable.

    Function Over Flash—Actual Use-Cases

    For those not immersed in synthesis, it may seem surprising just how much value 4-Bromo-2,6-Difluoroiodobenzene brings to complex molecule construction. The placement of bromine and iodine lends itself to selective cross-coupling reactions. Chemists aiming for Suzuki, Stille, or Ullmann-type couplings benefit from this clean functionalization—one position ready for palladium-catalyzed attachment, another for further transformation. The two fluorine atoms aren’t just decorative—they actively tune the electronic character of the ring, changing reactivity and influencing the behavior of downstream products. This proves particularly valuable in the design of active pharmaceutical ingredients or specialty materials where electron distribution dictates performance.

    Our lab teams regularly field calls from research chemists needing an intermediate that resists unwanted side reactions in multi-step syntheses. The precise substitution pattern here delivers fewer impurities post-reaction, shortening purification times. That means better results, less solvent waste, and fewer resources spent reworking material that doesn’t meet specs. From a manufacturer’s vantage, direct interaction with end-users provides us with unique insight into what features actually matter to chemists on the ground.

    Comparison—Distinguishing Markers from Similar Benzene Derivatives

    Some ask how 4-Bromo-2,6-Difluoroiodobenzene measures up against more common dihalogenated or trifluorinated benzenes. Experience teaches us that while many aromatic halides can be interchanged in simple couplings, nuanced substitution patterns play a decisive role in more advanced structures. Products like 1,3-dibromo-5-fluorobenzene or 2,4,6-trifluoroiodobenzene often lack the highly specific reactivity necessary for stepwise derivatization. The arrangement here—bromine at position 4, fluorine at 2 and 6, with iodine at 1—engineers orthogonal reactivity. This means users can exploit one halogen’s chemistry without disturbing the others, enabling two different types of bond-forming reactions on the same scaffold.

    We’ve run test comparisons in-house, assessing how reaction rates and yield profiles shift when moving from our product to more generic halobenzenes. The difference is stark: yields climb, side products decrease, and time saved in column workups increases. That’s not just an advantage in the lab—it reduces solvent and energy consumption, which matters in a world where operational sustainability is becoming a regulatory matter as much as a practical one.

    Manufacturing Footprint—True Production at Source

    Manufacturing this compound isn’t a matter of rebranding someone else’s product. Every lot begins with raw chemical feedstocks sourced with traceability in mind. Our reactors don’t just follow a recipe—they run under conditions adjusted for seasonal variations, solvent recovery rates, and the performance of catalysts on hand. Through repeated process improvement exercises, we’ve narrowed down catalyst choices, solvent mixes, and temperature paths that maximize throughput without sacrificing controllability.

    Our technology team worked for years to iron out bottlenecks in halogen exchange reactions. Iodine-halogen exchanges, notoriously finicky under certain conditions, were optimized to bring the iodo function into place with minimum byproduct formation. Every improvement, no matter how slight, gets logged and referenced for subsequent batches—a benefit unique to those who stand over their product from start to finish.

    Most importantly, the people handling 4-Bromo-2,6-Difluoroiodobenzene know the risks and protocols firsthand. Cooling, containment, and safe transfer procedures were tailored around our own continuous use of this intermediate. Documentation at each stage isn’t just for external audits but enables us to investigate any anomaly with full transparency. By investing in our own staff’s expertise, returns in reliability, safety, and yield follow naturally.

    Challenges in Production—Meeting Modern Expectations

    Producing complex aromatic intermediates such as 4-Bromo-2,6-Difluoroiodobenzene doesn’t unfold without challenges. Many of the persistent issues—impurity carryover, solvent recovery losses, or shifts in reagent quality—demand hands-on troubleshooting. There’s a temptation, especially for traders and distributors, to treat off-spec batches as “good enough” for certain regions. We reject this mindset and have seen firsthand how small upgrades in process control return major benefits over time.

    The regulatory climate has sharpened requirements for control of trace metals, waste stream minimization, and full material traceability. Our facilities invested early in real-time chromatography and advanced analytics, making it possible to assure customers and partners that every purchase aligns with both domestic and international standards. We’ve welcomed external process validation, knowing our dedication to self-inspection means easier navigation in export markets.

    Another ongoing task involves harmonizing scale. Research labs might need only a few grams; specialty materials manufacturers calculate their needs in hundreds of kilograms per month. Our process engineers built flexibility into production lines to accommodate this range without significant downtime or cross-contamination risk. Each format—sample vials, PE drums, composite-lined cartons—comes filled directly on site, with all filling and sealing performed under conditions that maintain the compound’s integrity.

    Knowledge Grown from the Plant Floor

    Longevity in chemical manufacturing offers a perspective missing from indirect sellers. Decades of operating at scale translate into a sort of intuition: missing tiny impurities before they appear in formal analysis, knowing the likely effect of atmospheric changes on a crucial crystallization step, anticipating when a drum lot might need extra QC. Newcomers to the plant learn to spot these subtleties with exposure and mentoring, something rarely available at a trading desk.

    This lived experience manifests in the finished product. Regular audits, unexpected customer requests, or sudden changes in regulatory guidance don’t send us scrambling. Established internal protocols and in-house analytical resources handle verification, root cause analysis, and corrective actions with practiced routine. That enables us to offer transparency to our customers—answers come from the people who actually make what’s in the drum.

    Emergencies sometimes arise—a vessel overload, a shortfall in a key precursor, unforeseen storage conditions leading to caking. We learned not to hide these events but to work out root causes openly, reshaping training and SOPs as a result. It’s not process documentation for its own sake, but a lived, growing framework that keeps quality and safety standards high.

    Supporting Chemists and Innovators Directly

    Large or small, our customers share some core needs: speed in delivery, predictability in outcome, and technical support that doesn’t drown them in generic answers. We see research partners running cutting-edge transformations, developing new drugs, or tackling environmental technologies. These new projects demand flexibility. A batch that deviates needs troubleshooting, not just a replacement box. Open lines of communication—chemist to chemist—often prevent weeks of wasted effort down the line.

    A recurring theme involves discussing planned synthesis steps before an order is finalized. Some users require 4-Bromo-2,6-Difluoroiodobenzene with a guarantee on residual trace metals. Others focus on the moisture content or compatibility with a peculiar coupling reagent. Years of close work with top research institutions and material companies made us better at handling the idiosyncrasies of each case. Instead of pushing “one size fits all,” we address particular, sometimes unexpected, demands with direct adjustments to lab or plant practice.

    Whether a customer pursues milligram-level structure-activity studies or engineers a new polymer platform, the underlying requirements trace back to advantages built into the 4-Bromo-2,6-Difluoroiodobenzene structure. The robustness and specificity reflect both the science behind the molecule and the judgment of those who manufacture it again and again, year after year.

    Environmental Responsibility—Doing the Work, Not Just Talking It

    Public scrutiny of chemical manufacturing’s impact has intensified across regions, but this pressure can drive innovation. Our site manages emissions, recycling, and water use continually. Solvent recovery units capture and purify more than 85% of recycling-eligible liquids each month. Spent catalyst beds, a perennial concern in halogenation facilities, feed established recovery and metals reclamation programs.

    On several occasions, scrutiny by local authorities led us to refine reaction protocols, not only reducing the load on our effluent systems but saving raw input costs as well. Our process engineers, environmental chemists, and line workers meet regularly to share updates and explore further optimizations. Making these improvements as a manufacturer means feedback loops are short—if a problem emerges, we have both authority and responsibility to address it without waiting for corporate change orders from afar.

    Some industry peers focus on image, rather than measurable improvements. By contrast, our daily working life revolves around measuring, controlling, and improving every process input and output. This mindset not only satisfies new regulatory pressures but often uncovers latent process improvements that raise yield or cut wastage, multiplying positive impacts.

    Future Outlook: Adaptation Guided by Experience

    Our experience tells us that fine chemicals, especially multi-halogen substituted aromatics, will continue to play a foundational role in the evolution of pharmaceuticals, agrochemicals, and advanced materials. Shifting demand means opportunities, but also increased scrutiny and more complex global compliance. By controlling each step in production, we built in resilience. New analytical instruments can drill down on previously undetected impurities, and new reaction methods promise major gains in efficiency or selectivity.

    We invest in team training, not just as a regulatory checkbox but as a guarantee that institutional knowledge passes from experienced hands to the next. Our technical staff remain engaged with national and international research networks, tracking breakthroughs in catalysis or process intensification techniques. This direct awareness enables rapid piloting and adoption of process innovations when they become robust enough for real use.

    Feedback from working chemists continues to inform both how we produce and how we supply 4-Bromo-2,6-Difluoroiodobenzene. By acting on specific, sometimes granular suggestions, we gradually expanded our format range, improved packaging, and adapted documentation to match global customer needs. Every improvement starts from an observation on the plant floor or a collaboration in the lab—not from idle speculation.

    Real Product, Real Accountability

    Being a chemical manufacturer reveals the tangible impact of consistent practice, skilled problem-solving, and openness to feedback. For us, 4-Bromo-2,6-Difluoroiodobenzene isn’t just a catalogue entry. Its reliable performance grows out of real process mastery and respect for the chemists who build the next generation of molecules using our work as their starting point. We make this compound ourselves, bear responsibility for every batch, and stand ready to talk not just about specifications but about every lesson learned along the way.