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4-Bromo-3-Fluoroanisole

    • Product Name 4-Bromo-3-Fluoroanisole
    • Alias 4-Bromo-3-fluoro-1-methoxybenzene
    • Einecs 841-422-5
    • 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

    325014

    Chemical Name 4-Bromo-3-Fluoroanisole
    Cas Number 2625-98-9
    Molecular Formula C7H6BrFO
    Molecular Weight 205.03 g/mol
    Appearance Colorless to pale yellow liquid
    Boiling Point 210-214 °C
    Density 1.601 g/cm3
    Refractive Index 1.555
    Smiles COC1=CC(=C(C=C1)Br)F
    Synonyms 4-Bromo-3-fluoro-1-methoxybenzene
    Purity Typically ≥98%

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

    Packing & Storage
    Packing Amber glass bottle, 25 grams, sealed with a screw cap; features hazard labeling, product name, chemical formula, CAS number, and supplier details.
    Shipping 4-Bromo-3-Fluoroanisole ships in tightly sealed containers, protected from light, moisture, and sources of ignition. It is typically transported as a hazardous chemical, classified under UN1993 (flammable liquid), following all applicable regulations for flammable liquids. Appropriate labelling, safety documentation, and temperature control are ensured during shipping to maintain quality and safety.
    Storage 4-Bromo-3-Fluoroanisole should be stored in a tightly sealed container in a cool, dry, and well-ventilated area, away from direct sunlight and incompatible substances such as strong oxidizers. Store at room temperature and avoid exposure to moisture. Label the container clearly, and keep it in a designated chemical storage area. Ensure appropriate spill containment and access to safety equipment.
    Application of 4-Bromo-3-Fluoroanisole

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

    4-Bromo-3-Fluoroanisole serves as a critical intermediate for advanced organic synthesis in select industrial sectors. As direct producers, we supply this specialty chemical to clients in the agrochemical, pharmaceutical, specialty materials, and electronics precursor segments. Below, we detail specific application fields and integration requirements.

    1. Agrochemical Intermediate Synthesis

    4-Bromo-3-Fluoroanisole functions as a key halogenated aromatic starting material in the synthesis of novel insecticide and herbicide actives. Formulation chemists leverage its unique substitution pattern to construct fluorinated phenoxy- and anilinic frameworks used in selective crop protection agents. This compound enters first-step coupling or substitution reactions to install reactive sites and introduce desired electronic effects. Strict control of residual solvents and by-products is maintained to support formulation stability and regulatory dossiers for finished plant protection products.

    Industry compliance standards

    • FAO/WHO International Code of Conduct on Pesticide Management
    • EU Regulation (EC) No 1107/2009 on Plant Protection Products
    • REACH Registration (EC 1907/2006) for intermediates
    • ISO 9001:2015 for consistent batch manufacturing

    Typical usage ratio

    • 0.3 to 0.8 molar equivalents per synthetic route, depending on target molecule
    • Adjustment based on active ingredient target yield and reaction efficiency

    Downstream process integration

    • Initiation of Suzuki or Buchwald-Hartwig coupling for diaryl ethers
    • Direct nucleophilic aromatic substitution for herbicidal amide cores
    • Integration during multi-step active substance construction
    • Purification to minimize cross-contamination in formulation plants

    Final product types

    • Selective herbicides (e.g., fluorinated phenoxyacetic acid analogues)
    • Specialized insecticides for resistant pest management
    • Active ingredient concentrates for field dilution
    • Pre-mix technicals for downstream formulation blending

    2. Pharmaceutical Building Block

    As an essential aryl halide, 4-Bromo-3-Fluoroanisole enables the construction of fluorinated biaryl motifs and ether linkages in small-molecule pharmaceuticals. Medicinal chemists employ this intermediate in late-stage active pharmaceutical ingredient (API) synthesis where regioselectivity and substitution precision are crucial. The product is synthesized in GMP-audited facilities, with batch traceability and documentation suitable for submitting to regulatory agencies. Application-specific purification ensures removal of potentially genotoxic impurities for downstream medicinal chemistry.

    Industry compliance standards

    • ICH Q7A Good Manufacturing Practice for APIs
    • USP/NF and Ph. Eur. reference monographs for related substances
    • 21 CFR Part 211 Current Good Manufacturing Practices
    • ISO 13485 traceability support for clinical development

    Typical usage ratio

    • 0.1 to 0.5 molar equivalents per targeted coupling or etherification step
    • Titration based on batch size and process development data

    Downstream process integration

    • Direct Suzuki-Miyaura coupling for active API analogues
    • Methyl ether deprotection as needed in API synthesis
    • Process control for carryover minimization to final drug substance
    • Integration in pilot and scale-up stages with dedicated QA/QC protocols

    Final product types

    • Branded and generic oncology therapeutics (e.g., kinase inhibitors)
    • Fluorinated CNS-active agents (e.g., antidepressants, antipsychotics)
    • Final API for formulated oral solid dosage and injectable products
    • Pharmaceutical intermediates for further modification

    3. Electronic Chemical Precursor for Liquid Crystals

    Manufacturers of advanced display materials incorporate 4-Bromo-3-Fluoroanisole into custom liquid crystal monomer synthesis. Its fluorine and bromine groups introduce strong dipole moments and facilitate alignment needed for high-performance nematic or smectic phases. Careful adjustment of the aromatic substitution enables fine-tuning of optical and dielectric properties. This raw material is delivered in high-purity form under stringent moisture and particle controls suitable for cleanroom integration.

    Industry compliance standards

    • IEC 61249-2-21: Requirements for halogen-free base materials
    • ISO 14001:2015 for environmental management in chemical processing
    • RoHS Directive (2011/65/EU) for restricted substances
    • Factory-validated product change control procedures

    Typical usage ratio

    • 0.2 to 1.0 weight percent in liquid crystal mixture formulations
    • Optimized based on birefringence and viscosity balancing requirements

    Downstream process integration

    • Upstream coupling or condensation into core liquid crystalline monomers
    • Vacuum and inert atmosphere handling to mitigate by-product formation
    • Direct supply to display panel material houses for batch compounding
    • Integrated in automated small-molecule blend lines

    Final product types

    • Nematic and smectic liquid crystal mixtures for LCD fabrication
    • Active material matrices for OLED alignment layers
    • Specialty film coatings for TFT applications
    • Optically anisotropic polymers for advanced display technologies

    4. Specialty Polymer Modification

    Chemical engineers utilize 4-Bromo-3-Fluoroanisole as a functional monomer or reactive modifier for specialty fluorinated polymers. Its aryl halide unit enables grafting or copolymerization with performance resins, imparting enhanced thermal and chemical stability as well as improved flame retardancy. This raw material is combined with initiators or catalysts under precisely controlled temperature and pressure in closed reactor systems. End uses include niche coating materials and high-demand plastic components for electronic and aerospace sectors.

    Industry compliance standards

    • UL 94 Standard for Flammability of Plastic Materials
    • ASTM D638 for polymer mechanical property testing
    • ISO 11469 plastics identification and traceability
    • IEC 60695 standards for fire hazard testing in device housings

    Typical usage ratio

    • 1 to 5 mol% as a comonomer or chain-end modifier
    • Proportion varies by target molecular weight and application property goals

    Downstream process integration

    • Direct addition into prepolymer or reactive extrusion processes
    • Copolymerization with acrylates, styrenics, or fluorinated vinyls
    • Chain-end functionalization during thermostatic control polymerizations
    • On-line QC monitoring for substitution completion and uniformity

    Final product types

    • Flame-retardant wire and cable jacketing
    • Conformal coatings for printed circuit boards
    • Precision-engineered polymer components for aerospace fittings
    • High-performance films for sensor and actuator devices
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    Certification & Compliance
    More Introduction

    4-Bromo-3-Fluoroanisole: A Vital Building Block in Modern Chemical Synthesis

    Introducing 4-Bromo-3-Fluoroanisole

    Our journey with 4-Bromo-3-Fluoroanisole stretches back over a decade, and in our manufacturing facilities, this compound has taken on a significance that many in the industry might overlook. With the growing demand for unique halogenated intermediates, we have focused our efforts on refining the production and supply of this specialty molecule. Since 4-Bromo-3-Fluoroanisole brings together methylation and dual halogenation, it stands apart in its reactivity, selectivity, and effectiveness within a variety of end-use applications.

    Chemical Profile and Production Considerations

    As hands-on producers, we’ve fine-tuned the synthesis of 4-Bromo-3-Fluoroanisole through years of experience. The chemical structure itself — a benzene ring bearing a methoxy, a bromine, and a fluorine group — demands careful handling of each substituent during manufacturing. Our process consistently achieves high purity, and we address trace-level impurities through targeted post-synthetic treatments and real-time process controls.

    Conventional anisoles rarely host both bromo and fluoro substituents on adjacent positions, but this differentiation grants 4-Bromo-3-Fluoroanisole unique versatility compared to more common anisole derivatives. The placement of substituents influences reactivity: researchers have demonstrated increased selectivity in cross-coupling and functionalization reactions involving this compound. We’ve witnessed firsthand in customer feedback how these properties translate to higher yields in pharmaceutical and agrochemical projects.

    Why 4-Bromo-3-Fluoroanisole Matters for Developers

    Many in the industry focus on common intermediates, but the world of specialty molecules is where innovation flourishes. Our customers, primarily engaged in pharmaceutical, fine chemical, and advanced materials development, look to us for high-integrity products that remove roadblocks at the synthesis stage.

    4-Bromo-3-Fluoroanisole became a popular choice among chemists developing new active pharmaceutical ingredients (APIs) and crop protection agents. The specific arrangement of bromo, fluoro, and methoxy groups enhances electron distribution on the aromatic ring. This tunable electronic profile improves coupling efficiency in Suzuki-Miyaura reactions and similar transformations. In our experience supplying batches to various research groups, order repeat rates climb highest for those working on routes where other isomeric anisoles fail to deliver consistent reactivity or selectivity.

    Pharmaceutical R&D prioritizes selectivity, yield, and cost-effectiveness. By relying on 4-Bromo-3-Fluoroanisole, chemists reduce the number of steps needed to introduce halogen substituents or methoxy protection. Streamlined synthetic sequences cut down on waste and unnecessary purification, two factors always at the forefront of modern manufacturing priorities.

    Differences from Other Anisole Derivatives

    With direct experience producing a range of substituted anisoles, differences between 4-Bromo-3-Fluoroanisole and its close siblings become clear. For example, 4-Bromoanisole remains widely available but lacks the additional fluorine, which contributes both electronic and steric effects. The fluorine atom, even though small, exerts a surprising impact on ring activation. This change influences regioselectivity in further substitutions.

    We’ve reviewed literature and conducted our own field studies on differences in reactivity, especially in coupling and C–H activation chemistries. In real production runs, we observe that the fluorinated variant, thanks to its electronic influences, often results in both higher yields and fewer byproducts. These operational advantages trickle down to our customers, who feed the output directly into critical, value-adding synthetic operations. Waste handling, always a significant cost consideration, also becomes simpler because unwanted side reactions drop measurably.

    Substituted anisoles bearing single halogens often suffer from predictability issues in multi-step synthesis. The dual substitution pattern in 4-Bromo-3-Fluoroanisole provides unique handles for chemists—making it easier to guide subsequent modifications. This is particularly useful when building complex scaffolds, such as those found in oncology or CNS pipeline molecules. Our experience confirms the demand for this compound in projects aiming for greater target selectivity or receptor subtype isolation.

    Consistency, Purity, and Traceability from the Manufacturer

    As original manufacturers, we treat the reproducibility of 4-Bromo-3-Fluoroanisole as a matter of pride. Our QC practices involve continuous spectral monitoring (NMR and GC-MS), batch homogenization, and highly sensitive contamination checks. Detecting trace amounts of isomeric or residual byproducts is a non-negotiable part of our process. Industry partners routinely return to us after struggling with inconsistent supplies from non-manufacturing traders or brokers.

    Over the years, customer audits and regulatory reviews have strengthened our own oversight. Supply chain transparency is a necessary part of our operation, so each lot can be traced back through production records, batch logs, and raw material sources. Chemists working in the field have explained to us that traceability helps them respond to regulatory queries more smoothly, which directly impacts their ability to register new products in major markets.

    Use in Today’s Synthetic Challenges

    It’s easy to take a robust chemical intermediate for granted, but the reality emerges in pilot batches or during scale-up. Once a route leaves the research bench, the demands on input material quality tighten. Any variability—impurity spikes, inconsistent moisture levels, micrograms of heavy metal carryover—leads to headaches down the line.

    We produce 4-Bromo-3-Fluoroanisole under strictly controlled temperature and pressure regimes. Our purification stages strip away color bodies, volatile residues, and off-odor compounds. Several multinational R&D groups have stressed to us that the hallmark of a reliable chemical partner is predictable, batch-after-batch performance. Breakdowns are rare, and these typically tie back to raw material volatility. By building strong relationships with our upstream partners, we avoid much of the turbulence that affects traders or distributors, who may not control or even know the original production source.

    Handling this compound presents relatively few risks compared to other halogenated species. It exhibits good shelf stability, a manageable vapor pressure, and no exceptional affinity for moisture or oxygen. Nevertheless, every stage from raw material distillation to finished material packing is executed to prevent contamination or degradation. Experience has taught us that seemingly minor deviations—an extra hour in a non-inert atmosphere or protracted heating—may result in yellowing or the rise of trace phenolic impurities, both of which slow down downstream purification.

    Practical Insights from Scale-Up

    A manufacturer’s real-world insights often differ from speculative literature. During scale up, we’ve noted that agitation, feed rate of precursor reagents, and precise order of addition greatly affect crystallization and overall recovery. For example, the timing of bromination relative to fluorination determines not just yield, but impurity formation. Through iterative batch runs, we achieved high yields while avoiding structurally similar impurities.

    Waste minimization forms a core objective for every campaign. Over years of producing various fluorinated and brominated anisoles, we’ve upgraded solvent recovery technologies and switched to less hazardous quenching agents for post-reaction work-up. For our buyers, this means a product whose footprint aligns with increasingly stringent environmental expectations. The process modifications also help to drive down costs, a benefit we pass directly on to our partners.

    Reducing Downtime with Manufacturer Reliability

    In project management, procurement delays cause the greatest headaches—not just for chemists but for purchasing departments and business development. Having weathered supply bottlenecks in the past, we maintain a safety stock of 4-Bromo-3-Fluoroanisole in climate-controlled storage. Batch sizes are tailored to both kilogram and metric ton requirements, which lets us support everything from early-stage discovery to competitive tendering for commercial synthesis.

    Our logistics team manages documentation, transport, and compliance without subcontracting steps. This direct involvement safeguards the product from delays tied to third-party handling or customs-related holdups. Both Asian and Western buyers have voiced appreciation for real-time order tracking and technical support, which we deliver without the communication lag typical of multi-tiered supplier chains.

    Innovation Driven by Feedback

    At the heart of our business sits a commitment to continual improvement, grounded in regular exchanges with front-line scientists and process engineers. Over the years, feedback has prompted us to fine-tune drying parameters, extend quality control tracking, and launch new packaging formats that reduce static or cross-contamination risk. By attending customer lab audits and observing their actual operational challenges, we’ve learned how even modest formulation changes—such as a drop in residual solvents—can save hours in downstream column operations.

    This two-way flow of information, rarely present in distributor-driven supply chains, strengthens both sides. A pharmaceutical developer recently pointed out that our improved lot labeling simplified traceability for their clinical batches. An agrochemical partner noted a reduction in byproduct formation in final formulations, a direct byproduct of our upgraded purification steps.

    Moving Beyond Commodity Supply

    4-Bromo-3-Fluoroanisole, for us, represents a shift away from the commodity mentality that plagues parts of the chemical trade. The compound’s value derives not just from its price or physical specifications, but from the predictability, support, and traceability embedded in every lot.

    New entrants into the field, especially those focused on green synthesis or sustainable chemistry, increasingly demand manufacturer-level engagement. Questions about process safety, solvent use, and waste minimization loom as large as traditional pricing. By documenting our process improvements and welcoming third-party audits, we empower both our customers and ourselves to meet emerging regulatory and societal expectations.

    Emphasis on Knowledge, Experience, and Transparency

    Building trust among end users doesn’t rest on certificates alone. Years of hands-on experience making and handling 4-Bromo-3-Fluoroanisole—and learning from every challenge—enable us to provide more than just a molecule. We offer reliable solutions to recurring pain points: fluctuating purity, irregular supply, and confusing regulatory paperwork.

    Transparency underpins our operation. Production and quality data, raw material origin, and post-delivery support are always open for discussion. This ethos aligns with growing end-user demands for supply chain visibility and real-life support, both critical when developing new products or scaling up manufacturing.

    Addressing Sustainability and Regulatory Challenges

    Increasing scrutiny of halogenated intermediates’ environmental impact demands serious attention. We invest in solvent recycling, effluent treatment plants, and batch yield optimization to minimize waste. Auditors from leading pharmaceutical firms have validated our operations, both in terms of regulatory compliance and environmental stewardship. As international regulations tighten, our in-house documentation and monitoring prepare both us and our customers for swift adaptation.

    We actively discuss regulatory uncertainties with buyers, helping them understand product registration requirements in various jurisdictions. This collaborative approach shortens product launches and reduces the risk of regulatory setbacks.

    Looking Ahead

    Chemical synthesis continues to evolve, and so does the need for trustworthy, well-characterized intermediates. 4-Bromo-3-Fluoroanisole plays a pivotal role in modern synthetic routes, often quietly working behind the scenes to make breakthroughs possible. Drawing on practical manufacturing experience—not just theoretical know-how—ensures that the product delivered performs as intended from the very first batch to the last.

    We view our role not just as producers, but as partners. Our ongoing collaboration with R&D teams across fields—pharmaceuticals, agriculture, new materials—shapes the future of product development, both through the success stories and the lessons learned from honest setbacks. In a world where time to market and process reliability matter more than ever, our daily mission remains simple: deliver 4-Bromo-3-Fluoroanisole with the consistency and conscientiousness that only a dedicated manufacturer can provide.