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1-Bromo-4-Chloro-2-Fluorobenzene

    • Product Name 1-Bromo-4-Chloro-2-Fluorobenzene
    • Alias 1-Bromo-2-fluoro-4-chlorobenzene
    • Einecs 841-834-8
    • 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

    791393

    Name 1-Bromo-4-Chloro-2-Fluorobenzene
    Molecular Formula C6H3BrClF
    Molecular Weight 209.44 g/mol
    Cas Number 57311-92-7
    Appearance Colorless to light yellow liquid
    Boiling Point 208-210°C
    Density 1.72 g/cm³
    Refractive Index 1.558
    Purity Typically ≥98%
    Solubility Insoluble in water; soluble in common organic solvents
    Synonyms 2-Fluoro-1-bromo-4-chlorobenzene
    Smiles FC1=CC=C(Cl)C=C1Br
    Inchi InChI=1S/C6H3BrClF/c7-4-1-2-5(8)6(9)3-4/h1-3H

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

    Packing & Storage
    Packing 100 mL amber glass bottle with tight-seal cap, labeled "1-Bromo-4-Chloro-2-Fluorobenzene," includes safety symbols and batch information.
    Shipping 1-Bromo-4-Chloro-2-Fluorobenzene is shipped in tightly sealed, chemically resistant containers to prevent leaks and contamination. It must be transported according to local and international regulations for hazardous substances, typically within labeled packaging, accompanied by a safety data sheet (SDS), and handled by trained personnel to ensure safe delivery and storage.
    Storage Store **1-Bromo-4-Chloro-2-Fluorobenzene** in a tightly closed container in a cool, dry, and well-ventilated area, away from direct sunlight and incompatible substances such as strong oxidizers. Keep the chemical away from heat and open flames. Ensure proper labeling and use secondary containment to prevent leaks or spills. Follow all relevant safety and regulatory guidelines for storage.
    Application of 1-Bromo-4-Chloro-2-Fluorobenzene

    Applications of 1-Bromo-4-Chloro-2-Fluorobenzene in Industrial Manufacturing

    As the original manufacturer of 1-Bromo-4-Chloro-2-Fluorobenzene, we supply this intermediate to specialized industrial sectors with strict demands on synthesis, purity, and regulatory compliance. Our material undergoes rigorous QC and controlled batch tracking to meet downstream production standards. Below, we detail genuine application scenarios based on direct customer use and industry feedback.

    1. Agrochemical Active Ingredient Synthesis

    Major agrochemical producers incorporate 1-Bromo-4-Chloro-2-Fluorobenzene as a halogenated precursor in the custom synthesis of advanced herbicide and fungicide active substances. This compound reacts via nucleophilic aromatic substitution and subsequent coupling steps to introduce tailored moieties, improving crop protection molecule stability and selectivity. Manufacturing standards demand high control of impurity levels, including trace halogen content, to avoid adverse interactions and environmental risks. Technical documentation supports registration dossiers and multi-site product deployment.

    Industry compliance standards

    • REACH (Regulation EC No 1907/2006) Registration and Safety Data Sheet compliance
    • EPA TSCA Inventory for US import and downstream processing
    • Food and Agriculture Organization (FAO) Specification standards for crop protection actives
    • ISO 9001:2015 certified quality management protocols

    Typical usage ratio

    • 8–15% by mole in key intermediate synthesis (final dosage adjusted based on structure-activity optimization for target crop protection agent)

    Downstream process integration

    • Charged as a first- or second-addition aromatic ring in semi-batch reactors
    • Halogen-exchange and coupling reactions for side-chain variation
    • Directly upstream of API crystallization and downstream wet-milling for formulated concentrate preparations

    Final product types

    • Commercial herbicidal technical concentrates
    • Triazole- and sulfonylurea-based fungicides
    • Seed treatment suspensions
    • Pre-mix formulations for broad-acre crop application

    2. Pharmaceutical Intermediate for Anti-Cancer APIs

    Global pharmaceutical manufacturers employ this aryl halide as a key intermediate when constructing heterocyclic scaffolds for targeted oncology therapeutics. It serves as both a coupling substrate and as a building block for fluorinated biaryl motifs, contributing to improved metabolic stability and binding sensitivity. Precise input ratios and impurity control are essential, as downstream GMP operations require full traceability and batch record integration up to the final API release. Documentation covers route validation and regulatory filing.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice Guide for Active Pharmaceutical Ingredients
    • US FDA cGMP (21 CFR 210/211)
    • EU GMP Volume 4, Part II
    • USP/EP/JP relevant monographs for related compounds (if applicable)

    Typical usage ratio

    • 5–12% by weight in target heterocycle ring formation reactions (dosage optimized per synthetic route and downstream building block constraints)

    Downstream process integration

    • Acts as starting material in Suzuki or Buchwald–Hartwig coupling
    • Reductive amination and targeted fluorination for active side-chain elaboration
    • Integration prior to chiral separation and purification steps

    Final product types

    • API intermediates for kinase inhibitor drugs
    • Fluorinated benzamide-based anticancer APIs
    • Specialty cytostatic bulk substances

    3. Liquid Crystal and Display Material Precursors

    Electronics-grade material manufacturers use this compound in the synthesis of custom fluorinated aromatics, which form the basis of advanced liquid crystal molecules for LCD and OLED display panels. The fluorine, bromine, and chlorine substituents enable tunable dielectric and optical properties, enhancing response time and contrast. High-purity grades with ultra-low metal and ionic contamination are required for integration into precision electronics. Production batches follow strict traceability and technical documentation for original equipment manufacturer (OEM) specifications.

    Industry compliance standards

    • IPC-4101B (laminate quality for electronics)
    • RoHS Directive 2011/65/EU for hazardous substances in electronics
    • IEC 62321 for halogen/fluorine analytical methods
    • ISO/IEC 17025 for QC laboratory testing

    Typical usage ratio

    • 2–8% as a functional monomer precursor in multi-step synthesis (adjusted for display type and molecular structure being targeted)

    Downstream process integration

    • Condensation and halogen-exchange reactions for LCM synthesis
    • Polycondensation for complex liquid crystal host matrices
    • Direct integration with purification columns prior to mixture formulation

    Final product types

    • Active liquid crystal host molecules for TFT and IPS panels
    • OLED intermediate monomers
    • Electronic display alignment films

    4. Fine Chemical Building Block for Dye and Pigment Manufacturing

    Dye and pigment producers utilize 1-Bromo-4-Chloro-2-Fluorobenzene as a precise halogenated aromatic substrate. Its role as a coupling partner in azo, anthraquinone, and perylene dye synthesis enables unique color profiles and improved fastness properties for technical textiles, industrial inks, and high-value plastics. Accurate molar input control ensures batch-to-batch consistency in color strength and thermal stability. QC documentation supports traceability and product stewardship for downstream consumer safety compliance.

    Industry compliance standards

    • OEKO-TEX Standard 100 for textile chemical approvals
    • EN 71-3 (Toy safety - migration of certain elements, relevant for pigment use)
    • ISO 14001 for environmental management in production facilities
    • REACH Annex XVII restrictions for certain aromatic amines

    Typical usage ratio

    • 3–10% by weight in primary dye-coupling stages (ratio tailored per chromophore intensity requirements)

    Downstream process integration

    • Input in batch reactors for aromatic coupling or substitution
    • Integration during sulfonation and diazotization for color diversity
    • Blending with dispersants prior to pigment milling

    Final product types

    • Reactive and disperse dyes for technical textile processing
    • High-stability pigments for plastics, coatings, and inks
    • Special-performance dyes for automotive and industrial fabrics

    5. Custom Chemical Synthesis for Polymer Additives

    Polymer additive manufacturers require 1-Bromo-4-Chloro-2-Fluorobenzene as a specialty building block when developing functionalized stabilizers and flame-retardant moieties for engineering plastics. Integration into multi-step organic syntheses produces structurally unique additives that raise oxidation resistance and thermal stability in high-performance polymers. This application requires well-defined isomer ratios, low residue levels, and batch records to support customer OEM audits and downstream REACH compliance.

    Industry compliance standards

    • UL 94 (Tests for Flammability of Plastic Materials)
    • REACH SVHC (Substances of Very High Concern) guidance for additives
    • ISO 9001-certified production and batch-traceability protocols
    • ASTM D5630 (Ash Content in Plastics for additive evaluation)

    Typical usage ratio

    • 2–6% in additive molecule synthesis (optimized according to polymer matrix and end-use thermal stability spec)

    Downstream process integration

    • Fed into closed reactor systems as a halogen-functionalized aromatic
    • Combination with phosphorus or nitrogen donors for flame retardant property
    • Blending into masterbatches for plastic compounding

    Final product types

    • Heat-resistant polymer stabilizers for nylons and polyesters
    • Halogenated flame-retardant additives for engineering plastics
    • Specialty UV absorber precursors for outdoor-use compounds
    Free Quote

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    Certification & Compliance
    More Introduction

    Insight Into 1-Bromo-4-Chloro-2-Fluorobenzene: Value, Performance, and Real-World Experience

    Introduction to 1-Bromo-4-Chloro-2-Fluorobenzene

    Chemistry often deals in subtleties. Over the decades of manufacturing halogenated aromatic compounds, we have learned that small alterations in a molecule’s structure make a real difference—sometimes tightening the window for success, sometimes unlocking whole new applications. Among the compounds we consistently address, 1-Bromo-4-Chloro-2-Fluorobenzene has provided a unique solution to a narrow set of challenges. Those who work with organic synthesis or custom intermediates recognize its distinct fingerprint. Behind every drum or bottle that leaves our facility, there stands a team that understands why specific substitutions matter—on paper, on the benchtop, and in the plant.

    Defining the Compound: Practical Chemistry Meets Performance

    The molecular structure of 1-Bromo-4-Chloro-2-Fluorobenzene is anything but arbitrary. Our process delivers a consistent halogenated aromatic with three distinct substituents, each providing a function grounded in practice. This specific pattern—a bromine at the first carbon, chlorine at the fourth, and fluorine at the second—stems from practical requirements in downstream chemistry. Its CAS number tags it for reference; in reality, success is achieved in real reactions, not catalogs.

    This compound’s boiling point, reactivity, and stability—features we have measured in our labs—allow tight control over arylation, cross-coupling, and other aromatic transformations. These properties do not come about by chance: every batch is run under strict process conditions, filtration, purification, and quality control routines. We know how trace impurities or slight variations in isomer ratios hurt confidence and performance; feedback from hundreds of technical users shapes each step on our end.

    The quality one receives from the source shapes downstream results. We maintain a schedule of intermediate and final analyses to catch off-spec materials early. With each order, chemists receive a product that clears the typical benchmarks for trace metals, organic residuals, and water, supporting robust reproducibility in scale-ups and sensitive syntheses. The technical specialists who have worked with both high- and low-grade material understand the hidden costs of poor reproducibility—a lesson everyone ought to learn only once.

    Comparing the Compound: Not All Halogenated Benzenes Are Equal

    Surfaces scanned under GC and NMR do not always capture what matters in a real plant. 1-Bromo-4-Chloro-2-Fluorobenzene stands apart from simple dichlorobenzenes or trifluorobenzenes in its cross-reactivity and selectivity in key reactions. Fluorine, known for its electron-withdrawing ability, increases the aryl ring’s resistance to reduction while modulating reactivity for Suzuki, Stille, and Ullmann couplings; this enables access to building blocks unreachable with simpler halogenations. Bromine and chlorine, each with their own patterns of leaving group ability and sterics, further tune the molecule’s attributes, offering precise distinction in reactivity compared to straight dibromo or dichloro analogs.

    Some chemists ask why they should opt for a triple-halogenated product rather than settling for a mixed dihalide or a single-fluorinated version. The answer reveals itself during attempts to generate regioselective products or make active pharmaceutical ingredients with chiral or steric demands. Our long-term collaborators in the pharmaceutical and agrochemical fields often arrive at 1-Bromo-4-Chloro-2-Fluorobenzene after testing series of alternative routes and running up against unwanted byproduct formation or difficult separations. Substitution at three positions steers subsequent transformation towards specific regioisomers, reducing process complexity in a way that is hard to replicate with other molecules.

    In bulk chemical use, cost per kilogram is one metric. We have seen, time and again, that reduced waste streams and cleaner downstream purifications offset supposed price advantages of alternatives. The fewer chromatographic steps one runs, the lower the solvent demand and labor investment. So from the synthetic chemist’s side, the appeal lies in both cost-efficiency and success rate. For those handling large-scale reactions or developing new synthetic routes, failing to use the right intermediate carries a pain that stretches all the way through to the final product yield and purity.

    Our Experience: Keeping Specifications Relevant and Reliable

    Supplying a molecule such as 1-Bromo-4-Chloro-2-Fluorobenzene at commercial volumes means the work never stops at simply meeting minimum standards. Years ago, we realized that a specification only holds value if it matches real-world requirements. At the bench scale, a trace of a regioisomer might escape detection; on a multi-kilogram scale, it can shut down an entire process. Our QC protocols reflect feedback not just from internal labs but also from companies scaling pilot batches or seeking regulatory compliance.

    Customers expecting fair and full answers often seek details on melting points, color, odor, purity, and packaging to match the complexities of their projects. We built our process to give straightforward answers. Every batch comes with full analytical documentation—NMR, HPLC, GC-MS profiles—so chemists know what they are getting. We continue to tie our manufacturing standards to ongoing feedback from both established and innovative end-users. Few things slow progress like inconsistent shipments; our goal is always to put reliability first.

    Storage and transportation also factor into success. Over time, we have worked to refine containers, moisture controls, and handling protocols to reduce the risk of degradation or physical damage. This work includes stability studies under ambient and variable temperature and humidity ranges. From drum to flask, maintaining integrity preserves performance—an aim we share with every user, regardless of their application’s scale.

    End-Use Applications: What Sets This Intermediate Apart

    Pharmaceutical organizations regularly come looking for building blocks that speed up their development programs. They often turn to 1-Bromo-4-Chloro-2-Fluorobenzene after paper-based retrosynthesis points towards more complex heterocycles or fluoroaromatic scaffolds. The molecule’s steric and electronic patterns steer selectivity in modern cross-couplings, SNAr reactions, or multistep transformations. Over years spent serving this sector, the demands for purity and process transparency have helped us fine-tune batch homogeneity and documentation practices.

    Agrochemical developers approach this compound with requirements for aggressive process efficiency. Compared to analogs, the three-halogen pattern often supplies a launchpad for target compounds requiring subsequent functional group modifications. At higher volumes, we have worked with teams to develop campaigns that minimize downtime and batch-to-batch variability. In such competitive fields, the reliability of the starting material often makes or breaks a season’s product output.

    Electronic materials manufacturers have grown reliant on precision halogenated aromatics as they design new functional polymers or specialty coatings. 1-Bromo-4-Chloro-2-Fluorobenzene brings unique reactivity, allowing fine-tuned electronic properties not possible with simpler benzenes. Through direct collaboration, we help integrate this molecule into process flows where any deviation in composition threatens function and value.

    Lessons From Production: The Value of Consistency

    Years of scaling up production on this compound have proved one thing: cutting corners on halogen source quality, solvent preparation, or post-synthesis processing never pays off. Even a modest uptick in side-product formation, detected as early as in-process GC, amplifies through the batch. Cleaning up after problems at this stage costs time and money, whether through additional columns or increased rework. That’s why we have doubled down on fixed raw material sourcing, validated every new lot, and invested in continuous process improvements. These steps were born out of necessity and out of respect for the chemists who depend on each shipment.

    Plant engineers in our team often trade notes after post-campaign reviews, identifying sources of loss or variation. One lesson arrives repeatedly: uniform halide loading and precise reaction control minimize downstream headaches. We have retooled everything from filtration rigs to packing lines in response to trends detected by clients and our own teams; sometimes, a small tweak in agitation or dosing solves what would otherwise be a weeklong troubleshooting exercise.

    Recalls and rejections are not abstract business risks. They impose direct reputational and practical costs. Listening to users who report on rare out-of-spec incidents or anomalous results has driven us to seek root causes methodically, logging events and passing new preventive or corrective controls into our CAPA system. This culture of transparency—while sometimes hard-earned—keeps our material trusted and useful, batch after batch.

    Environmental Considerations and Sustainability

    Attention has moved far beyond basic hazardous waste disposal. Responsibility for halogenated aromatic wastes, emissions, and process residues falls squarely upon manufacturers like us. Current environmental standards leave little room for complacency, especially for producers dealing in bromo- and chloro-organic intermediates. Over the years, we have reduced solvent use, introduced capture and scrubber systems for off-gassing, and pursued return/recovery programs for byproduct streams.

    Treating effluent and managing solid residues requires significant technical input. We design in line with local and global best practices—aiming at waste minimization and full compliance. Sometimes, the only way forward is a costly upgrade to abatement facilities or process redesign. Our clients benefit indirectly from these investments, since downstream regulatory pressures increase with each passing year, especially in export markets. We see compliance not as a checklist, but as a continual improvement cycle, shaped in collaboration with customers, auditors, and community stakeholders.

    Day-to-day, our teams look for opportunities to reclaim, purify, and reuse as much material as practical. Every solvent recaptured, every kilogram of byproduct reprocessed, and every emission abated yields real savings and supports long-term access to global markets. Being able to document and defend our performance in these areas matters as much as the technical performance of 1-Bromo-4-Chloro-2-Fluorobenzene in the final application.

    Process Safety and Handling: Always A Priority

    Manufacture of halogenated organics demands strict oversight on safety due to their inherent reactivity and volatile byproducts. In our operations, exposure controls, regular training, and engineered safeguards form the routine backbone of activity. Not a month passes without inspection and testing of ventilation, spill response, and operator PPE protocols. For users, understanding proper handling ensures product stability and personnel protection—training that we reinforce with regular information updates and real-world feedback from the field.

    Logistics teams update their best practices based on the real behaviors of the product—how it responds to temperature swings, transit vibration, or extended storage. This information, exchanged between supplier and user, helps reduce unplanned losses and deferred shipments. Our ongoing challenge is to adapt quickly to the specifics of each delivery route and to keep refining our safeguards as regulations evolve.

    Supporting Innovation: Working With Chemists, Not Just Supplying Material

    The work of a manufacturer doesn’t stop at delivery. Our technical and R&D staff often partner directly with users attempting novel transformations, troubleshooting reaction quenching, or seeking higher selectivity. These practical collaborations deliver more than a material supply—they offer an ongoing exchange that keeps us at the leading edge of usability. We regularly provide in-depth feedback on compatibility with emerging palladium, nickel, or copper-catalyzed coupling conditions; these small contributions often ease route scouting for new chemical entities.

    In developing supply agreements or process optimization campaigns, we work hand in hand with innovation teams at customer sites. Teams benefit from our direct knowledge of the quirks—thermal stability, sensitivity to certain acids or bases, long-term storability—that can break or make a new pathway. Through joint milestone planning, we help integrate the compound into complicated production schedules and regulatory filings, boosting confidence that each batch will support advancement without surprise delays.

    What We Have Learned: Commitment To Progress

    The chemical landscape keeps shifting—both technically and commercially. Decades of work with halogenated intermediates like 1-Bromo-4-Chloro-2-Fluorobenzene taught us that attention to real user needs counts for more than certifications alone. It takes experience-driven oversight, open feedback loops with clients, and continual investment in both process and people to keep material useful and trusted. We have seen direct benefits in reduced downtime, fewer scale-up failures, and smoother campaign launches. That commitment to improvement runs through every kilo of product, every conversation with a technical user, and every new campaign that depends on clean, reliable supply.

    Detailed, process-driven oversight now runs side by side with environmental and safety imperatives. Technical teams, from our synthetic chemists to our QC and logistics specialists, treat every shipment as a reflection of the care built into each step along the way. We appreciate the trust that users place in our ability to deliver not just a product, but a partnership that respects science, schedules, and shared success.

    Closing Reflections: The Manufacturer’s Perspective

    Materials such as 1-Bromo-4-Chloro-2-Fluorobenzene rarely generate headlines, but they shape the pace and safety of countless downstream developments. Chemistry is not a business of shortcuts. Years of hands-on work, real feedback, and open communication underpin the processes that carry a molecule from raw starting materials to a finished, ready-for-reaction intermediate. Every batch tells a story of adaptation, learning, and technical rigor. Serving chemists, engineers, and companies that want practical solutions means more than just supplying a regulated product—it means standing behind everything that leaves the plant, every time.