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4-Methoxy-3-(Trifluoromethyl)Bromobenzene

    • Product Name 4-Methoxy-3-(Trifluoromethyl)Bromobenzene
    • Alias 1-Bromo-4-methoxy-3-(trifluoromethyl)benzene
    • Einecs 841-696-5
    • 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

    399848

    Product Name 4-Methoxy-3-(Trifluoromethyl)Bromobenzene
    Cas Number 139469-09-9
    Molecular Formula C8H6BrF3O
    Molecular Weight 255.03 g/mol
    Appearance Colorless to pale yellow liquid
    Boiling Point 138-140°C at 760 mmHg
    Density 1.63 g/cm³
    Purity Typically ≥98%
    Refractive Index n20/D 1.505
    Flash Point 62°C
    Solubility Insoluble in water, soluble in organic solvents

    As an accredited 4-Methoxy-3-(Trifluoromethyl)Bromobenzene 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 25 grams of 4-Methoxy-3-(Trifluoromethyl)Bromobenzene, labeled with chemical name, structure, and hazard symbols.
    Shipping 4-Methoxy-3-(trifluoromethyl)bromobenzene is shipped in sealed, chemical-resistant containers, protected from light and moisture. It should be handled as a hazardous material, following all relevant regulations for flammable and toxic substances. Shipping is typically via ground or air freight, with proper labeling and documentation to ensure safe transport and delivery.
    Storage Store 4-Methoxy-3-(Trifluoromethyl)Bromobenzene in a tightly sealed container, protected from light, moisture, and incompatible substances such as strong oxidizing agents. Keep it in a cool, dry, well-ventilated area, ideally in a chemical storage cabinet. Ensure proper labeling and restrict access to trained personnel. Use appropriate personal protective equipment when handling the chemical.
    Application of 4-Methoxy-3-(Trifluoromethyl)Bromobenzene

    Applications of 4-Methoxy-3-(Trifluoromethyl)Bromobenzene in Industrial Manufacturing

    As a manufacturer specializing in high-purity aromatic intermediates, we supply 4-Methoxy-3-(Trifluoromethyl)Bromobenzene primarily to innovators across pharmaceutical synthesis, agrochemical actives, advanced material modification, and specialty dye manufacturing. Our chemical supports your complex downstream reactions, meeting industry expectations for quality and compliance throughout various production environments.

    1. Pharmaceutical API Intermediate Synthesis

    Pharmaceutical manufacturers incorporate this compound as a strategic halogenated building block in the preparation of fluorinated API scaffolds, particularly for central nervous system agents and oncology candidates. Its electron-withdrawing and methoxy functionalities enable site-selective Suzuki and Buchwald-Hartwig couplings for active moiety assembly, supporting critical steps in late-stage medicinal chemistry. Precise addition rates and GMP tracking ensure consistent, regulatory-compliant results from pilot scale to commercial batches.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • European Pharmacopoeia (Ph.Eur.), USP <797>
    • FDA 21 CFR Parts 210/211
    • EMEA guidance on impurities in new drug substances

    Typical usage ratio

    • Used at 0.5%–5% w/w of total reaction mass. Dosage varies with target API molecular weight and the number of halogen exchange steps; reaction stoichiometry optimized based on required substitution and scale-up yields.

    Downstream process integration

    • Dosed during intermediate or penultimate step in multi-stage API synthesis, usually introduced during Pd-catalyzed cross-coupling reactions followed by purification and crystallization stages.

    Final product types

    • Fluorinated small-molecule pharmaceuticals (e.g., CNS agents, kinase inhibitors)
    • Advanced heterocyclic API intermediates
    • Reference standards for chemical analysis

    2. Agrochemical Active Ingredient Manufacture

    Leading agrochemical producers rely on this aromatic building block during the synthesis of selective herbicide and fungicide intermediates, where both trifluoromethyl and brominated motifs are essential for biological activity optimization. The compound is added at specific condensation or substitution steps to control the introduction of functional groups, ensuring field efficacy and regulatory acceptance of final products.

    Industry compliance standards

    • FAO/WHO Specifications for Agrochemical Technical Material
    • ISO 9001:2015 Quality Management System for Crop Protection Production
    • REACH Regulation (EC) No 1907/2006 for EU market access
    • China National Standards GB/T 1605 (Pesticides)

    Typical usage ratio

    • Added at 1%–3% by weight relative to the target molecule formation step, with adjustments based on molecule design and impurity management protocols.

    Downstream process integration

    • Introduced during Grignard or organometallic coupling syntheses of aromatic amines, then followed by chlorination or ring-closure for bioactive structures; in-line quality checking for residual bromide content prior to final formulation.

    Final product types

    • Fluorinated herbicide and fungicide precursors
    • Active ingredient concentrates for crop protection
    • Stabilized pre-formulated granules

    3. Electronic and Specialty Material Functionalization

    Advanced materials manufacturers use this compound to induce specific electron-density profiles in organic semiconductors, OLED emitter building blocks, and specialty polymers. The introduction of both trifluoromethyl and methoxy substituents allows fine-tuning of charge carrier mobility, thermal resistance, and band gaps in high-value structural materials for electronics and sensors.

    Industry compliance standards

    • IPC-4101B (Base Materials for Rigid and Multilayer PCBs)
    • RoHS Directive 2011/65/EU for hazardous substance limits
    • ISO/TS 80004-8 (Nanotechnologies for Material Characterization)
    • REACH Regulation (EC) No 1907/2006 for material safety

    Typical usage ratio

    • Incorporated at 0.1%–2% of total monomer or oligomer feed, calculated for target polymer backbone length and property requirements; bench-scale optimization precedes scale-up to coil, film, or powder production.

    Downstream process integration

    • Introduced during electrophilic aromatic substitution or Suzuki polymerization, acting as a key functionalized monomer segment; post-functionalization involves controlled annealing or solvent casting.

    Final product types

    • Organic electronic devices (OLED, OFET components)
    • High-performance specialty polymer films
    • Semiconductive sensor substrates

    4. Fluorinated Dyes and Pigments Manufacturing

    Manufacturers of specialty dyes and high-stability pigments formulate with this aromatic intermediate to achieve enhanced solubility, unique color attributes, and weatherfastness. The ring system architecture, featuring both a methoxy and trifluoromethyl group, supports direct attachment to dye cores for textile, laser, or technical colorants, with robust performance even in aggressive processing or application environments.

    Industry compliance standards

    • OEKO-TEX Standard 100 for textile chemicals
    • EN 71-3 Safety of Toys (Migration of Certain Elements for Pigments)
    • ISO 18451-1:2015 (Pigments and Extenders Terminology)
    • GHS Chemical Labeling for pigment precursor handling

    Typical usage ratio

    • Dosed at 0.5%–2% of the total dye/pigment intermediate weight, adaptable for batch or continuous processing, and fine-tuned for chromatic intensity and solubility targets in the downstream application.

    Downstream process integration

    • Added during azo-condensation or electrophilic aromatic substitution in multi-step dye development, followed by drying, milling, and blending processes according to end-use (e.g., fiber spinning, ink preparation).

    Final product types

    • Textile printing dyes (fiber-reactive, acid, or disperse types)
    • Special effect pigments for technical coatings
    • Colorant intermediates for inkjet and laser printing
    Free Quote

    Competitive 4-Methoxy-3-(Trifluoromethyl)Bromobenzene prices that fit your budget—flexible terms and customized quotes for every order.

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    Certification & Compliance
    More Introduction

    4-Methoxy-3-(Trifluoromethyl)Bromobenzene: A Chemist’s Perspective

    Direct from the Manufacturer’s Floor

    Every new intermediate owes its performance to the process, the work on the instrument bench, and the experience built into its manufacture. In our plant, 4-Methoxy-3-(Trifluoromethyl)Bromobenzene reflects that effort from start to finish. We make this compound in batches where every step is tracked, starting with raw material verification through to post-synthesis purification. With years on the floor, we've learned that reproducibility isn't just about hitting numbers on a spec sheet; it relies on knowing your chemistry, your solvents, and every reaction that feeds into the final yield.

    What 4-Methoxy-3-(Trifluoromethyl)Bromobenzene Brings to Synthesis

    In the world of specialty aromatic halides, this molecule stands out for a reason. Our production emphasizes the importance of a clean trifluoromethyl group positioned opposite that bromine, and keeping a tight rein on isomeric byproducts. We’ve heard from researchers that even a hint of regioisomer throws off downstream coupling reactions, so our route prioritizes selectivity by homing in on conditions that shut down competitive substitution.

    Why pursue a structure like this? Adding both the trifluoromethyl and the methoxy group onto the benzene core unlocks reactivity no simple bromoarene can deliver. The electron withdrawal from the CF3 group tempers the ring, balancing methoxy contribution to electron density—this fine-tuning often proves essential in modern synthesis. For medicinal chemists or agrochemical researchers, fine differences at this level often translate into breakthroughs when tailoring molecules for activity or selectivity.

    What Experience Teaches About Purity and Consistency

    Anyone who has scaled up aryl halide couplings in a lab knows the trouble a persistent impurity can cause. Over the years, we've seen that purity in starting material influences everything downstream—from yield to reproducibility to regulatory approval. We’ve worked hard to bring 4-Methoxy-3-(Trifluoromethyl)Bromobenzene to a standard that doesn't just meet specs on paper but responds consistently to cross-coupling or lithiation.

    With each lot, we sample and check by GC and NMR—because sometimes a hidden contaminant slips below HPLC detection, but not the trained chemist’s eye. We don’t chase the lowest cost, but the tightest possible specification, because every solvent wash and extra crystallization step pays off for the end user by saving troubleshooting further down the synthetic chain.

    Applications Shaped by Real Work

    This compound has found its way into libraries of heterocycles, pharmaceutical intermediates, and new material prototypes. In-house, we test each batch in Suzuki and Buchwald-Hartwig couplings to confirm it holds up in high-throughput screens and demanding research projects. One thing many chemists want to know: does this bromobenzene stand up to competitive products in catalyst performance, reaction time, or scale-up? From our bench, the answer comes from our roots in synthesis, not marketing. Our main priority is reliable halogen transfer—bromine activation without dragging along hard-to-remove fluorinated byproducts.

    Every time we ship to a lab, we include a recent chromatogram and spectra. Not every competitor does this, but our years in manufacture have taught us that few things frustrate a project more than uncovering a hidden impurity after weeks of work. There’s pride for us when customers call back with positive feedback, and no detail is too small to get right.

    How Our 4-Methoxy-3-(Trifluoromethyl)Bromobenzene Differs from Commodity Aromatic Halides

    Making specialty chemicals can be thankless work to those outside the lab, but subtle differences in manufacturing shape every gram of product. Cheap or rushed bromination pushes side reactions; day-to-day process inattention leads to color, odor, or impurity drift. Our approach holds to multi-stage purification, fresh catalyst, filtered solvents and constant monitoring for even trace contaminants. This approach doesn't scale the way trading brokers hope—meaning, we ship smaller volumes more often, recalibrating and watching for cumulative signals of process drift.

    There are plenty of ways to shortcut process control: moving quickly, skimping on raw material checks, or trusting older instruments. From where we stand, those choices creep back into consistency, and eventually, the reliability your customer sees in their own development timeline. Our compound isn't just another item on a shelf—it has to deliver to that last decimal point in high-stakes synthesis, where small errors compound over time.

    Best Practices Developed from Decades in Manufacture

    Not all processes can be copied from literature to industrial scale. Early in our development, we found that even tiny shifts—temperature, agitation, purity of trifluoromethyl sources—reveal themselves batch by batch. We worked to map these dependencies to avoid unpleasant surprises for our customers. In analytical QC, we never drop below verification by both NMR and GC. There’s no substitute for checking, even when a run looks perfect at first glance.

    Environmental and health considerations matter on the shop floor. The plant’s solvent recovery system captures and purifies for reuse, which not only lowers overall impact but also keeps trace solvent impurities out of the finished product. Protective measures don't only keep our team safe—they keep contamination away from high-value product stocks. We believe that a well-run plant is seen in small details: from the clarity of the final solution to the absence of visible solids or color cast.

    Listening to Customers and Developing the Next Process

    After every batch goes out, we collect feedback from researchers and process chemists who are deep in their development work. Some call out improved solubility, others push for lower-percentage contaminants. We've rebuilt parts of our purification line more than once based on that feedback. While we hold to consistent specs, we listen when a customer finds a challenge and needs tighter limits for their process—whether that means an extra polish before packaging, or further confirming our compound’s identity by advanced mass spectrometry.

    For many years, we worked only at tens-of-gram batches, which suited prototyping and R&D. With more interest from process development clients, we upscaled while maintaining our in-house testing approach at every step. The experience in scaling up without hidden surprises, chemical incompatibilities, or new batch-to-batch deviations, comes only through trial, error, and direct chemical know-how.

    Why Specifications Matter to Us—Not Just Compliance

    Sometimes the requested purity may seem overcautious. In our experience, it's not until one tracks a difficult step to a contaminant months later that the full impact becomes clear. Because trifluoromethyl and methoxy groups demand such different control, we've spent more time on method validation for their detection than on bromine content. Cross-contamination, even at trace levels, carries into multi-step syntheses where those traces can get amplified and interfere, whether in isolation or in the biological assays that often follow.

    We hardly ever see pure white product when the process isn’t spot-on. Slight off-colors, unusual flow properties under the scoop, or a delayed reaction on test scale—all these prompt a review and a repeat. We once caught a small drop in final methylation based solely on the crystal habit at the end of drying. Our staff’s attention to detail, day after day, keeps surprises at bay, rather than relying strictly on formal inspection points.

    Field Reports: Successes and Hard Lessons

    In process chemistry, nothing replaces the realities learned from pilot and commercial campaigns. We once received bulk product returned for off-odor, only to find a source batch solvent that had pooled out of spec. Small things produce big effects; since then, every vessel and container goes through cleaning and solvent flush checks before reuse.

    Our partners developing new antifungal pharmaceuticals ran into unexpected byproduct peaks in their catalyst screens—they wrote detailed notes and, after several iterations, our analysis flagged a low-level byproduct from an early step we hadn’t tracked closely enough. This feedback loop led to a mid-process filter change and made that downstream route both more predictable and more cost-efficient over the next runs.

    Pharmaceutical clients pay us the highest compliment by coming back for new kilo lots after a tough regulatory review. The attention we gave to low-level impurities let their regulatory submissions sail through analytical scrutiny. Longer-term, this trust returns dividends in collaborative development, as we often get early looks at new structure-activity relationships using our compound as the aromatic scaffold.

    Comparisons—Beyond Basic Aromatic Bromides

    Generic bromobenzenes may fill out a catalog, but the differences become clear once researchers start synthesizing target molecules with specific demands. The trifluoromethyl and methoxy substitution gives our compound a profile that simply isn't matched by basic monosubstituted bromides or even some isomeric analogues. Fluorochemistry brings stability, shifts reactivity, and can dramatically improve shelf-life of a parent molecule.

    We’ve tracked competitive lots: some turn up yellow, others have visible particulates or are more sluggish under common Pd-catalyzed reactions. As a manufacturer, we troubleshoot origin rather than reroute complaints to a supplier. If a process fails, it’s on us to replicate the result in house, find a root cause, and fix it—not deflect responsibility.

    Among the main differences, our strict attention to solvent system and exact reaction stoichiometry means we avoid the small yield-sapping side-products that show up in legacy routes. There isn’t a shortcut for that—the knowledge and skill come from repeating manufacturing cycles and observing carefully. Our team’s memory and logbooks form part of every batch, as do the years of troubleshooting and hands-on adjustment.

    Supporting Sustainable Development through Manufacturing Rigor

    We know better than most how fine chemical manufacturing often faces criticism for waste and environmental impact. Over years, we’ve implemented solvent recovery, recycling wherever feasible, and rigorous energy management. Beyond certifications, these choices save on costs and, more importantly, show up in the finished product’s consistency. Cleaner operations lead to cleaner product, less downtime, fewer recalls, and a better result for final users.

    Technical development and environmental safeguards have to become part of the same equation. In producing 4-Methoxy-3-(Trifluoromethyl)Bromobenzene, a better process produces both a better product and more responsible use of materials from extraction to packaging. Our internal goal is not just to meet compliance requirements but to exceed them at every opportunity.

    Long-Term Collaboration Over Quick Transactions

    We value ongoing relationships with chemists, research institutions, and process experts more than any short-term shipment. Every inquiry begins a series of shared notes—a back and forth over conditions, findings, and real-world results. For every new run, we see the cumulative benefits: more robust process conditions, fewer troubleshooting calls, and a deeper understanding that lets both parties innovate.

    Every sample, every feedback cycle, and every analytical result is a data point. We log and compare these across runs, adjusting for those flashes of insight that only direct experience provides. Years of partnership with demanding customers have honed not just our manufacturing, but how we communicate, adapt, and learn together.

    The Value of Direct Manufacture: Trust Built Batch by Batch

    We produce 4-Methoxy-3-(Trifluoromethyl)Bromobenzene because we know the place this compound holds in research and industry. It’s never just a number, a label, or a trade item. Each batch stands as a record of skill, problem-solving, and commitment to quality that only grows deeper the longer we work.

    Our process—hands-on, direct, and unmediated—shows up in every container we ship. We see ourselves as the stewards of not just molecules, but of every research and production campaign they enter. We carry the lessons of each successful shipment and each rare setback into tomorrow’s batch. From our experience, the most valuable commodity is trust: earned on the plant floor, verified by analytical results, and proven in the labs where real work happens.