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4-Bromo-2-(Trifluoromethoxy)Iodobenzene

    • Product Name 4-Bromo-2-(Trifluoromethoxy)Iodobenzene
    • Alias 1-Bromo-3-iodo-5-(trifluoromethoxy)benzene
    • Einecs 839-588-0
    • 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

    183179

    Product Name 4-Bromo-2-(Trifluoromethoxy)Iodobenzene
    Cas Number 886762-17-0
    Molecular Formula C7H3BrF3IO
    Molecular Weight 368.90
    Appearance White to off-white solid
    Purity Typically ≥98%
    Melting Point 54-58°C
    Solubility Soluble in organic solvents (e.g., DMSO, DMF)
    Storage Conditions Store at 2-8°C, keep container tightly closed
    Smiles FC(F)(F)Oc1cc(I)ccc1Br
    Inchi InChI=1S/C7H3BrF3IO/c8-4-1-2-5(13)6(3-4)12-7(9,10)11
    Synonyms 2-Iodo-4-bromo-1-(trifluoromethoxy)benzene

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

    Packing & Storage
    Packing Amber glass bottle with secure cap, labeled "4-Bromo-2-(Trifluoromethoxy)Iodobenzene, 5g, For Research Use Only," includes hazard symbols.
    Shipping 4-Bromo-2-(Trifluoromethoxy)iodobenzene is shipped in tightly sealed containers under inert atmosphere, with proper labeling according to hazardous material regulations. The chemical should be stored and transported at room temperature, away from moisture, heat, and incompatible substances. Shipping complies with international and local chemical safety guidelines, ensuring safe handling and delivery.
    Storage 4-Bromo-2-(Trifluoromethoxy)iodobenzene should be stored in a tightly sealed container, protected from light and moisture. Keep it in a cool, dry, and well-ventilated area, ideally under inert gas such as nitrogen. Store away from incompatible materials, such as strong oxidizers and reducing agents. Always follow relevant safety protocols and consult the Safety Data Sheet (SDS) for specific storage recommendations.
    Application of 4-Bromo-2-(Trifluoromethoxy)Iodobenzene

    Applications of 4-Bromo-2-(Trifluoromethoxy)Iodobenzene in Industrial Manufacturing

    As a specialized manufacturer of advanced halogenated aromatics, we supply 4-Bromo-2-(Trifluoromethoxy)Iodobenzene to global partners engaged in high-value downstream synthesis. The following key application sectors represent the most established and compliant use cases for this material, particularly in regulated industrial and R&D environments.

    1. Pharmaceutical Intermediate Synthesis

    Leading pharma groups integrate this compound in the development and scale-up of small-molecule drug substances, especially within candidates having complex fluorinated and halogenated phenyl frameworks. Producers select this building block for Suzuki coupling, Buchwald-Hartwig amination, and various metal-catalyzed cross-coupling modules to create target motifs in oncology, CNS, and anti-inflammatory agents. All operational steps must align with electronic batch record systems, cGMP validation, and impurity tracking for later stage active pharmaceutical ingredients.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • EU EudraLex Volume 4 (Annex 21: Importation of active substances)
    • US FDA 21 CFR Part 211 (Current Good Manufacturing Practice for Finished Pharmaceuticals)
    • Chinese Pharmacopoeia (for domestic manufacturers)

    Typical usage ratio

    • 0.4 – 1.2 molar equivalents versus amine or boronic acid partners, depending on route optimization and impurity risk management

    Downstream process integration

    • Introduced during the cross-coupling or aromatic substitution phase under catalyst-specific conditions; process chemists control addition method for yield and purity

    Final product types

    • Active Pharmaceutical Ingredient (API) intermediates
    • Developmental drug candidates for oncology targets
    • Synthons for CNS, antiviral, and cardiovascular projects
    • Research reference compounds

    2. Agrochemical R&D and Synthesis

    Crop protection manufacturers utilize this halogenated benzene derivative as a key building block in the synthesis of novel fungicides and insecticides. Its reactivity profile supports the construction of fluorine-rich moieties, allowing for enhanced metabolic stability in field environments. Detailed impurity control and traceability systems ensure compliance across regional safety frameworks. Key steps include stepwise ligand attachment and late-stage modification to introduce bioactive substituents.

    Industry compliance standards

    • OECD Principles of Good Laboratory Practice (GLP)
    • ISO 9001:2015 Quality Management Systems for manufacturing sites
    • Regulation (EC) No 1107/2009, EU Plant Protection Products registration
    • US EPA Pesticide Registration Manual (for American facilities or registration)

    Typical usage ratio

    • 0.6 – 1.0 molar equivalents, fine-tuned based on desired residue limits and process validation outcomes

    Downstream process integration

    • Added to the synthetic sequence after core ring construction but before bioactive group derivatization; monitored for side product elimination via chromatography

    Final product types

    • Precursor intermediates for fluorinated, brominated, or iodinated agrochemicals
    • Research samples of new active substances
    • Scale-up batches for regulatory toxicity testing
    • Molecule discovery libraries

    3. OLED and Organic Electronics Materials

    Manufacturers of advanced optoelectronic materials (OLED emitters and transport materials) deploy this aromatic intermediate to construct electron-deficient cores with high triplet energy and tailored crystal packing. Used especially in blue and green emitter pathways, its dual halogen pattern facilitates subsequent C–C and C–N couplings that define device lifespan and emission profiles. All materials feeding into device applications undergo trace metal and solvent residue analysis in accordance with electronics industry protocols.

    Industry compliance standards

    • IEC 61340-5-1 (Protection of electronic devices from electrostatic phenomena)
    • RoHS Directive 2011/65/EU (Restriction of Hazardous Substances)
    • ISO 14644-1 Cleanrooms and controlled environments (Class 5-7 for OLED material synthesis)
    • Corporate device qualification protocols (Samsung, LG Display, BOE, etc.)

    Typical usage ratio

    • 0.8 – 1.3 equivalents, based on target molecular packing and required emission stability across large substrate areas

    Downstream process integration

    • Input to metal-catalyzed cross-coupling modules post purified core feedstock generation; downstream fractions isolated by preparative HPLC or crystallization for photophysical QC

    Final product types

    • OLED blue/green emitter molecules
    • Electron transport materials
    • Semi-conducting intermediates
    • Prototype batches for device testing and pilot lines

    4. Specialty Polymer and Advanced Material Monomers

    Functional polymer producers employ this iodo-bromo-trifluoromethoxy benzene in the design of custom high-performance polymers with targeted optical, chemical, or dielectric properties. Its utility lies in controlled cross-linking via aromatic substitution and step-growth polymerizations where fluorine and halogen substituents impact backbone rigidity, thermal stability, and surface energy. End uses range from display films and membranes to niche coatings, with suppliers expected to prove batch reproducibility and low levels of structural defects.

    Industry compliance standards

    • ISO 9001:2015 for Quality Assurance in Chemical Manufacturing
    • ASTM D6287-20 (Standard Guide for Identification of Polymers in Products)
    • REACH 1907/2006 (EU Regulation concerning the Registration, Evaluation, Authorisation and Restriction of Chemicals)
    • Specific customer-derived raw material approval protocols

    Typical usage ratio

    • 0.5 – 1.5 molar equivalents, adjusted based on target copolymer ratio and the polymerization method (step-growth vs. chain)

    Downstream process integration

    • Reactant in polymerization feedstocks following pre-mixed catalyst or initiator addition; integrated prior to molecular weight build-up and removed by extraction cycles if unreacted

    Final product types

    • High-Tg fluorinated polymers
    • Functionalized aromatic polyimides
    • Custom display and membrane films
    • Specialty coatings for electronics or aerospace

    5. Fine Chemicals and Analytical Standards Manufacturing

    Fine chemical producers use 4-Bromo-2-(Trifluoromethoxy)Iodobenzene in multi-step synthesis of unique molecular reference materials and analytical calibration products. Control chemists value its traceability and purity for the preparation of certified standards required by environmental and pharmaceutical testing laboratories. All critical steps follow ISO-certified weighing and documentation, with special focus on trace impurity identification by advanced NMR and MS methods.

    Industry compliance standards

    • ISO 17034:2016 (General requirements for the competence of reference material producers)
    • ISO/IEC 17025:2017 (Testing/calibration lab competence)
    • US Pharmacopeia (USP-NF) standards for reference standards
    • EU REACH substance registration for commercial sale

    Typical usage ratio

    • 0.2 – 0.9 equivalents, very tightly controlled by internal QC protocols to match stated purity/RRT specifications

    Downstream process integration

    • Added in designated steps for creation of final analytical standards post multi-stage purification; isolation by preparative chromatography mandatory

    Final product types

    • Certified reference standards for GC/MS, HPLC
    • Pharmaceutical impurity markers
    • Synthetic calibration substances
    • Custom chemical probes for research
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    Certification & Compliance
    More Introduction

    4-Bromo-2-(Trifluoromethoxy)Iodobenzene: Practical Insights from a Chemical Manufacturer

    Introduction

    People working in chemical synthesis look at starting materials and intermediates with a watchful eye, always weighing real-world production challenges against application needs. As someone involved in the daily grind of chemical manufacturing, I see 4-Bromo-2-(Trifluoromethoxy)Iodobenzene as a compound whose value comes both from its structure and the hands-on experience needed to keep quality consistent from batch to batch. Most customers speak about this material in terms of catalog numbers and molecular weights, but in our facility, it’s about method, process, and the specific hurdles faced every time we scale up.

    Beyond 4-Bromo: The Value of Dual Halogenation

    Compared to bromo- or iodo-monosubstituted benzenes, dual halogenation changes the playing field. With both a bromine and an iodine atom, chemists unlock more routes for Suzuki, Stille, or Sonogashira couplings and other cross-coupling chemistry. The selective reactivity—one site more labile than the other—lets medicinal chemists and materials scientists create advanced molecules with greater precision, targeting the order, timing, and conditions of each reaction step. Experienced manufacturers need to control not only the introduction of these halogens, but also avoid over-halogenation, debromination, or unwanted side reactions, especially when sensitive substituents like trifluoromethoxy are involved.

    Key Features and Specifications from the Factory Floor

    The molecule—officially known as 4-Bromo-2-(trifluoromethoxy)iodobenzene—takes the chemical formula C7H3BrF3IO. Purity tops customer requests, usually demanding greater than 98% by HPLC or GC for pharmaceutical work, though research and development users ask for batches tailored to their needs. White to off-white crystalline powder is the usual physical form, but color variations hint at process tweaks or contamination—a sign any manufacturer catches before it leaves inventory. Water solubility stays low; it dissolves more easily in common organics like DCM, THF, or DMF. Melting points generally land in the expected range, but thermal history and trace contaminants can shift it a few degrees, so every lot comes with its own measured data, checked against the last batch.

    Handling this compound involves more than ordering it by the drum. The trifluoromethoxy group complicates reactions under certain acidic or basic conditions. Scaling up for multi-kilogram lots brings up issues with stirring, filtration, and product isolation, where clumping or excessive fines signal impurities or poor crystallization. Over the years, refinements in workup steps like temperature-controlled filtration, careful drying, and rigorous in-house GCMS checks became the difference between repeat complaints and loyal customers.

    Applications in the Spotlight

    Chemists often ask how a new benzenoid intermediate will expand their toolkit. For our clients in medicinal chemistry, the dual halogen functionalities make this molecule appealing when constructing biaryl scaffolds for targets like kinase inhibitors, CNS penetrants, or advanced agrochemicals. They value selective halogen-metal exchange reactions, confident that skilled process development avoids side-products that complicate downstream purification. Some groups use it to introduce novel fluorinated motifs, exploiting the electron-withdrawing power of the trifluoromethoxy group to adjust metabolic stability or activity profiles in drug candidates.

    Beyond pharma, researchers in materials science and electronics dig into the properties brought by fluorine and halogen atoms. They look to alter band gaps or tweak molecular packing in organic semiconductors or liquid crystals. The compound lands in polymer chemistry as well, used in specialty copolymers or as a monomer building block, its reactivity giving rise to rare or proprietary structures. Realistically, these aren’t overnight breakthroughs—each project pushes the limits of reliability, and unexpected byproducts or bottlenecks in coupling reactions always bring new lessons for production chemists.

    Real Differences from Similar Halogenated Benzenes

    Customers compare 4-Bromo-2-(trifluoromethoxy)iodobenzene to chlorinated or single-halogen versions, expecting them to be interchangeable. The reactivity profile shifts more than the textbooks suggest, especially in large-scale or automated parallel syntheses. Iodine serves as the more reactive partner in most palladium or copper-catalyzed couplings, providing flexibility in stepwise functionalization. Bromine, less eager but still accessible, gives the synthetic chemist options in subsequent substitutions after the iodine leaves. This selectivity helps med chem teams design sequencing strategies for combinatorial array synthesis, enabling faster SAR exploration.

    What might look like a trivial change—adding a trifluoromethoxy group—profoundly impacts electron density and reactivity at the ring’s positions. Manufacturers face tougher purification, since this group can drag along similar byproducts and demand sharper separation in chromatography or crystallization. Even with state-of-the-art reactors, incorporating and preserving such substituents across scale-up complicates post-reaction workup. That’s where institutional process memory matters: running side-by-side comparisons of batches made through different routes, carefully tracking impurity markers, and processing customer feedback into concrete dispatch-to-dispatch improvements.

    Production Experience: Where Real Quality Emerges

    The raw numbers—assay percentages and spectral purity—only measure part of a manufacturer’s competence. Behind stable deliveries stand lessons learned from every misstep. Early on, moving from a hundred-gram scale to the first kilogram, we saw how solvent ratios and addition rates determine not just yield, but actual isolable product. Trifluoromethoxy benzenes can foam or form peroxides; strong attention to solvent grade and inert atmosphere protocols paid off with lower batch failure rates.

    Manufacturing isn’t just chemistry, it’s logistics and risk management. An unexpected delay in a halogenating reagent shipment or a shift in local humidity can threaten timelines or change product appearance. The right drying protocol at the end of the process—extended vacuum at modest temperatures, never rushing with heat—keeps material free-flowing and reduces lumps that frustrate formulation chemists. Every operator learns to check sample color and odor long before packing, since small changes indicate larger problems. Years of feedback from formulation labs and API groups shaped our decision to upgrade in-process filtration and implement full trace-level impurity benchmarking for each lot.

    Waste management keeps our process efficient and our compliance record clean. Dual halogenated streams complicate effluent treatment, so we invested early in capture and detoxification systems. Customers now ask detailed questions about residual metals, halides, and solvents in our output, so method validation and records matter—no batch leaves without a retained sample for future comparison. This builds trust, especially with buyers who use this intermediate for regulatory submissions and need documentation ready for audits.

    The Reliability Question: Consistency Through Change

    Synthetic chemistry trends come and go, but the people buying this intermediate rely on their suppliers to shield them from swings in raw material quality. We suffered early from “batch drift”—subtle variations in byproduct ratios from slight changes in precursor quality or minor recalibrations in reactors. The real fix took better training, stricter inventory control, and deep dives into every certificate of analysis. Implementing lot-specific testing for heavy metals and halogen content tightened our specs and let us communicate anticipated changes whenever a process tweak raised flags.

    Price volatility in raw halides and fluorinated reagents raises stress across the industry. We keep steady reserves of critical reagents, working with multiple vetted sources to smooth out market-driven shortages. Onboarding local suppliers for certain reagents reduced customs delays and let us address urgent customer projects that tolerate only narrow supply windows. We learned to communicate early and often, so buyers know what’s en route and chemists can pivot to contingency plans if needed.

    Addressing Synthetic and Quality Challenges

    Literature methods often work fine at milligrams, but scaling up reveals hidden headaches. Early runs produced unwanted polyhalogenated side-products, often stubborn to remove, especially when scaling to kilos. Introducing temperature stepwise addition helped slow competitive reactions. Stirrer speed and blade geometry, easily overlooked factors, emerged as key variables determining mixing efficiency and thermal distribution. We designed our own real-time sampling rig to catch process drift before it ruined a batch, letting us fine-tune parameters without waiting for the end-of-line assay.

    Quality control extends beyond purity alone. A customer once flagged glassy, sintered lumps in one lot—a drying artifact that seemed cosmetic but actually meant trapped solvent above acceptable limits. We encoded expanded loss-on-drying checks in our workflow, saving future lots from similar fate. Another pain point came from unreliable melting point measurements due to variable crystallinity caused by minuscule temperature fluctuations at the end of rotary evaporation steps. Adding a controlled-crystallization chamber stabilized this variance, yielding more reproducible lots and earning us renewed contracts with downstream pharma partners.

    Supporting Research and Industry Growth

    The real-world value of 4-Bromo-2-(trifluoromethoxy)iodobenzene lies in how it enables creative chemistry. From our vantage point, seeing how project teams deploy this molecule in new scaffolds and proprietary targets frames the manufacturing narrative in more than units shipped or kilograms produced. Material scientists explore pathways into OLEDs or fluorinated polymer backbones. Others in agricultural chemistry rely on the unique substitution pattern to reach herbicide analogs unreachable by simpler intermediates, finding routes that bypass restricted or tightly regulated precursors.

    We note patterns and trends: as regulatory lists evolve, researchers move away from problematic chlorinated intermediates toward fluorinated aryl compounds. This demand shift puts extra scrutiny on impurity profiles and documentation practices, so our investments in validated analytics and detailed batch history paid off long-term. Regular dialogue with innovators, not just procurement staff, reveals which specs need tightening and where batch records improve customer success. Each success story, in turn, refines how we analyze, process, and package subsequent lots.

    Environmental and Safety Considerations

    Dual halogenated compounds raise legitimate safety concerns. Trifluoromethoxy groups often mean volatility and reactivity beyond what casual users expect. Factory handling focuses on both the operator and the environment—fume hoods with upgraded scrubbing capability, sealed packaging lines, and robust PPE use see daily reinforcement. Teams undergo in-house training on spill management, minimizing exposure and avoiding downstream contamination. We support customers with technical sheets outlining best storage and handling, based on our own incident reports and near-miss tracking to provide support beyond the minimum compliance mark.

    Waste streams receive constant attention, especially during dark runs or system cleaning, which historically produced the highest concentration of halide-rich effluent. Early investment in closed-loop cat-ox systems and reagent recycling cut our waste, lowered disposal costs, and improved relations with clients under green chemistry mandates.

    Continuous Improvement Through Direct Feedback

    Long-term customers often share the realities of their downstream work. Every time a synthetic bottleneck or unexpected byproduct shows up, their reports give direction for our process tweaks. If a client’s coupling screen stalls from a stuck reaction or a batch of crude API fails purity check, it comes back down the supply chain to us. We assess chain of custody records, analyze retained lot samples, and run side-by-side tests with our reference specimens. These real-world stress tests reveal which process controls have room for reinforcement.

    Every lot gives feedback, though not always verbally: moisture uptake, subtle color changes, or even how the powder packs in a bottle help us catch issues before a dissatisfied customer does. We put our operators through “round table” reviews when recurring issues crop up, leveraging front-line experience for process solutions—sometimes that means revising quench steps, sometimes investing in new filtration media, other times simply training new staff to spot signs earlier. Over time, this collective practical knowledge inches us closer to the consistency that project leaders downstream count on.

    Building Trust with Every Batch

    Reliable suppliers don’t just react—they anticipate what matters to end users. That starts with a real understanding of the pain points researchers face, whether it’s frustration with slow or incomplete couplings, unexplained byproduct formation, or issues with drying and storage leading to batch failure. Our investment in in-house analytics, sample retention, and robust process documentation isn’t just to pass audits, but to trace any anomaly back to its source and institute fixes that protect the next batch. That’s the difference between a vendor and a partner in chemical manufacturing.

    Today’s buyers don’t merely evaluate a product—they weigh the process and the people behind it. Streamlined communication, transparent documentation, and a relentless focus on incremental improvements earn the orders that keep the line running. Over time, trust compounds, and as the demand for specialty intermediates like 4-Bromo-2-(trifluoromethoxy)iodobenzene grows, those relationships let everyone innovate and deliver with confidence.

    Closing Perspective

    Nobody in our factory views intermediates as mere commodities. Each new consignment of 4-Bromo-2-(trifluoromethoxy)iodobenzene mirrors the learning curve of everyone who touches the process, from early route design to kilo-scale dispatch. Real-world chemistry isn’t only about reactivity on paper—it’s about knowing how small process decisions ripple through production lines, impact product quality, and influence a project’s ultimate success. Facing the shifting challenges of raw material supply, regulatory requirements, and ever-stricter purity demands, only rigorous hands-on attention keeps quality consistent.

    The molecule’s unique mix of dual halogenation and trifluoromethoxy substitution expands what’s possible in modern synthesis, provided it’s made with an eye for practical detail—and that’s how we approach every batch. The best chemistry isn’t just what happens in the flask; it’s what survives the journey from plant to project, delivering repeatable results for everyone counting on it at the bench.