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2-Fluoro-4-Bromonitrobenzene

    • Product Name 2-Fluoro-4-Bromonitrobenzene
    • Alias 2-Fluoro-4-nitro-1-bromobenzene
    • Einecs 844-062-5
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry sales7@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    747463

    Cas Number 446-36-6
    Molecular Formula C6H3BrFNO2
    Molecular Weight 220.99
    Appearance Yellow solid
    Melting Point 48-52°C
    Boiling Point 288°C
    Density 1.81 g/cm³
    Purity Typically ≥98%
    Solubility In Water Insoluble
    Smiles c1cc([N+](=O)[O-])ccc1BrF
    Inchi InChI=1S/C6H3BrFNO2/c7-4-1-2-5(9(10)11)3-6(4)8/h1-3H
    Refractive Index 1.601 (estimate)
    Storage Temperature Room temperature
    Hazard Statements H315, H319, H335

    As an accredited 2-Fluoro-4-Bromonitrobenzene 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 25g of 2-Fluoro-4-Bromonitrobenzene, tightly sealed, labeled with hazard warnings and chemical details.
    Shipping 2-Fluoro-4-bromonitrobenzene is shipped in tightly sealed containers, protected from light and moisture. It is handled as a hazardous material, requiring appropriate labeling and documentation. Shipments comply with relevant regulations (IATA, DOT, IMDG), and are typically transported via specialized carriers trained for chemical transport and spill response.
    Storage 2-Fluoro-4-bromonitrobenzene should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from incompatible substances such as strong oxidizers and reducing agents. Avoid exposure to light and moisture. Store at room temperature and ensure proper labeling. Use chemical-resistant shelves and secondary containment to prevent spills or leaks.
    Application of 2-Fluoro-4-Bromonitrobenzene

    Applications of 2-Fluoro-4-Bromonitrobenzene in Industrial Manufacturing

    Our 2-Fluoro-4-Bromonitrobenzene supports specialized production processes in advanced pharmaceutical, agrochemical, plastics intermediate, and pigment manufacturing. By leveraging strict process controls and deep application experience, we supply clients who require precise compliance management, traceability, and advanced process integration for fine chemical synthesis and downstream operations.

    1. Active Pharmaceutical Ingredient (API) Intermediate Synthesis

    Pharmaceutical manufacturers utilize this compound as a strategic building block in multi-step syntheses for several fluorinated and brominated API precursors. Its ortho-bromo, para-nitro, and fluoro substitution pattern provides key reactivity for nucleophilic aromatic substitution, catalytic hydrogenation, and selective reductions, which are critical steps in small molecule drug manufacturing pipelines.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP-NF pharmacopeial monographs (as referenced for intermediates)
    • EudraLex Volume 4 GMP Guidelines (EU)
    • US FDA 21 CFR Part 211

    Typical usage ratio

    • Introduced at 0.2–0.8 molar equivalents relative to the target core scaffold; ratio varies based on the substitution stage and the specific API route.

    Downstream process integration

    • Added directly to the reaction vessel during aromatic substitution stages, typically following halogen-exchange or nitro-group transformations; process engineers optimize reagent loading and recycle protocols to control by-product formation and minimize impurities.

    Final product types

    • Pharmaceutical intermediates for kinase inhibitors, CNS drugs, and anti-infective compounds, including class-patented fluorinated benzene derivatives used in branded and generic medications.

    2. Agrochemical Active Ingredient Development

    Agrochemical formulators incorporate this material to construct complex benzene-ring systems for herbicide, fungicide, and insecticide projects where dual halogen and nitro substitution is essential. Both the electron-withdrawing fluoro and bromo groups direct selective synthesis, enabling stepwise assembly of bioactive crop protection molecules requiring high reaction reliability and low residual contaminant levels.

    Industry compliance standards

    • FAO/WHO Good Manufacturing Practice for Pesticide Production
    • OECD Guidelines for Testing of Chemicals
    • GB/T 1603-2011 (Pesticide technical requirements, China)
    • REACH Regulation (EC) No 1907/2006

    Typical usage ratio

    • Charged at 5–15% of the overall reactant mass in the target molecule formation step; percentage depends on the functionalization depth and required batch size in pilot or commercial runs.

    Downstream process integration

    • Fed into multi-step synthesis reactors from cleanroom-grade containers at the aromatic ring-building or coupling stage; engineers monitor stoichiometry to ensure repeatable conversion and facilitate waste minimization as dictated by environmental permitting.

    Final product types

    • Advanced intermediates for pre-emergent herbicides, nitrated benzene fungicide scaffolds, and active insecticidal components requiring regulatory registration and field safety validation before market approval.

    3. High-Performance Dye and Pigment Manufacturing

    Specialty dye producers source this compound for synthesizing halogenated and nitro-substituted aromatic pigments with enhanced lightfastness, chemical resistance, and tinting strength. The molecule’s configuration facilitates regioselective formation of color index azo pigments through controlled diazotization and coupling procedures intensive in pigment dispersion technology.

    Industry compliance standards

    • EN 71-3 Safety of Toys (European limits for colorants)
    • ISO 9001:2015 Quality Management Systems
    • REACH Annex XVII restricted substances (for non-toxicological pigment classes)
    • ETAD Code of Practice (Ecological and Toxicological Association of Dyes and Organic Pigments Manufacturers)

    Typical usage ratio

    • Reactant content typically 8–35% w/w in pigment synthesis batch, depending on desired colorimetric properties and product application (textile, plastics, inkjet ink systems).

    Downstream process integration

    • Introduced at the diazonium salt formation or azo coupling phase in pigment reactors; formulation specialists adjust ingredient chronology and pH to optimize chromaticity and minimize by-product colorants.

    Final product types

    • Azo pigments for printing inks, plastics masterbatches, technical textile dyes, and color dispersions used in advanced paint and coating systems.

    4. Fluorinated Polymer Intermediate Synthesis

    Polymer manufacturers use this chemical as a monomer precursor for engineering plastics and specialty fluorinated resins requiring tailored thermal and chemical properties. Its distinct substitution supports cross-linked or block copolymer architectures where halogen-rich intermediates deliver key performance advantages in flame retardancy or dielectric strength.

    Industry compliance standards

    • ISO 9001 Quality Management for Polymeric Materials
    • RoHS Directive 2011/65/EU (restrictions for electrical/electronic applications)
    • UL 94 Flammability Standard
    • ASTM D1929 Standard Test Method for Determining Ignition Temperature of Plastics

    Typical usage ratio

    • Loaded at 0.5–3 mole% as a comonomer or chain stopper, tuned according to end-use requirements including crystallinity, melt index, and flame resistance metrics.

    Downstream process integration

    • Pumped to the polymerization reactor during the solution or melt-stage synthesis as an active functional intermediate; downstream blending or pelletizing occurs after primary chain propagation and post-polymerization purification.

    Final product types

    • Modified engineering plastics, such as high-performance polyarylates, custom fluorinated polyesters, and specialty resins for wire insulation or electronics encapsulation.
    Free Quote

    Competitive 2-Fluoro-4-Bromonitrobenzene prices that fit your budget—flexible terms and customized quotes for every order.

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    Certification & Compliance
    More Introduction

    2-Fluoro-4-Bromonitrobenzene: Smart Chemistry Backed by Real-World Know-How

    Direct from the Manufacturer: Why We Focus on 2-Fluoro-4-Bromonitrobenzene

    In the chemical industry, trust and reliability stem from more than just meeting specifications. Decades of manufacturing experience have shaped how we approach specialty products like 2-Fluoro-4-Bromonitrobenzene. We understand what customers value: a clear product profile, batch-to-batch consistency, and technical support from people who actually produce and use these compounds. As the original manufacturer, days and nights spent on the production floor and in the lab put us in a unique position to share insights about this compound’s relevance and practicality in synthesis.

    About 2-Fluoro-4-Bromonitrobenzene: What Sets It Apart

    2-Fluoro-4-Bromonitrobenzene sits among the core building blocks of modern pharmaceutical and agrochemical research. On a molecular level, it features a fluorine atom in the ortho position and a bromine atom in the para position relative to the nitro group on a benzene ring. These choices are not accidental—they represent considered decisions backed by years of industrial and academic feedback. The juxtaposition of halogens and nitro group, for us, is about more than numbers on a GC report. It’s about predictable reactivity, reliable yield, and straightforward downstream processing.

    Not all halogenated nitrobenzenes behave the same way in a reaction vessel. We chose 2-fluoro and 4-bromo as substituents because, together, they create a platform for further transformations—such as nucleophilic aromatic substitution—while maintaining robust stability for storage or handling at scale. We’ve supported R&D chemists here and around the world as they respond to the shifting demands for novel intermediates. Many choose this molecule because it bridges the gap between cost-effectiveness and chemical versatility.

    Model, Form, and Specifications: A Close Look from a Manufacturer’s Perspective

    Only hands-on manufacturing reveals the little details that matter most. Our 2-Fluoro-4-Bromonitrobenzene is produced as an off-white to pale yellow crystalline powder—a sign of high purity and the absence of over-reduction or unwanted side reactions. Standard lots are typically 99% pure or greater by GC, but we track even trace-level impurities using high-sensitivity methods to ensure downstream application is unhindered. The molecular formula, C6H3BrFNO2, and molecular weight of approximately 220.99 g/mol, guide both our quality routines and our advice to our synthesis partners.

    As the manufacturer, we don’t deal in vague assurances. Lot records are traced from raw starting materials—fluoroanilines, brominating agents, selective nitrating mixtures—right through to finished packaging. Every step is documented and available for technical review, because end-users—especially in regulated industries—count on such transparency. Powdered form, controlled particle size, and consistent melting point (usually between 70-74 °C) keep reaction times and yields reliable from lab to plant scale. Filtration and drying are optimized to minimize residual solvents, which is not just a point of pride but a practical concern for users working under cGMP or ISO conditions.

    Why End-Users Choose It: An Insider’s View

    End-users ask hard questions. What can this compound build? How well does it work beyond the datasheet? In our experience, 2-Fluoro-4-Bromonitrobenzene steps forward in Suzuki couplings, Buchwald-Hartwig aminations, and nucleophilic substitutions. The aryl bromide moiety opens up palladium-catalyzed cross-coupling possibilities, essential for Chemists assembling biaryl scaffolds or introducing custom amine groups. The ortho-fluoro influence often increases selectivity, minimizing side products and wasted work-up time.

    Pharmaceutical innovators use it as a scaffold for small molecule development. The electron-deficient nature, courtesy of both nitro and fluoro, shifts reactivity in ways that enable precise synthetic control. Our partners in agrochemical research harness those same features to create new candidates for crop protection, herbicide innovation, and insecticidal studies. Functional group compatibility matters when whole project timelines run tight—even small shifts in coupling efficiency can impact months of R&D investment.

    Comparing With Other Halogenated Nitrobenzenes: What Users Should Know

    As the team responsible for large-scale manufacturing, we pay attention to feedback about adjacent products. Say, for instance, someone’s used 2-Chloro-4-Nitroaniline or para-bromonitrobenzene on their bench. The fluoro substituent in our molecule makes it stand out by providing a unique blend of reactivity and electron withdrawal not possible with chlorine alone. In lab trials, we’ve seen nucleophilic aromatic substitutions proceed more cleanly with a 2-fluoro group versus a 2-chloro, particularly when introducing amines or heterocycles.

    Take 4-Bromo-1-nitrobenzene: reliable for bromo-driven coupling, but it lacks the fluoro effect, which can be the difference between moderate and high conversion. One key learning from our process chemists is the fluoro group’s ability to stabilize intermediates—helpful for reaction pathways that encounter sensitive conditions. Where positional isomers like 3-fluoro-4-bromonitrobenzene sometimes lag in selectivity or stability, our 2-fluoro-4-bromo arrangement wins out in daily working conditions.

    From a practical standpoint, these differences are not theoretical—they play out in the volume of solvent required, the work-up steps, or the purity of end-products our customers bring back to us. We run comparison batches not to win a catalog contest, but to learn what works best at scale for both seasoned chemists and new labs pushing the boundaries.

    Quality Control: Lessons from the Production Floor

    We don’t leave quality to chance or routine. Every batch of 2-Fluoro-4-Bromonitrobenzene passes through our own labs—run by chemists who have both research and production experience. Over the years, we’ve seen how a small shift in reaction temperature, or a slight impurity in a starting material, can alter the final product’s color, melting point, or reaction profile. That’s why we commit to more than just releasing material after standard HPLC or GC runs. Our staff test reaction yield and side-product formation in application-driven scenarios, because many end-users have no time or budget to waste on surprises.

    Chromatographic purity, isomeric control, and moisture levels—these are not just specs in a binder for us. They reflect years spent troubleshooting unexpected bench results and learning the needs of real-world chemical synthesis. Several clients have mentioned how our documentation and data packages have helped their regulatory filings move faster. We’ve learned that experience-driven quality control, combined with transparent communication, keeps us accountable and relevant.

    Storage, Handling, and Practical Concerns

    Physical properties translate directly to real-world handling. 2-Fluoro-4-Bromonitrobenzene, being a solid at room temperature, stores well for extended periods under standard dry, cool warehouse conditions. Still, we go the extra mile by using double-sealed, inert containers sized for both kilo-lab and production scale. Our warehouse staff routinely review storage protocols, so customers receive fresh, stable product time after time.

    Hazards, though relatively routine for trained professionals, call for attention. As a nitroaromatic, this product requires proper gloves and eye protection, and its dust should be managed with well-maintained extraction. We stress this in every shipment and routinely field calls from plant technicians who want practical, no-nonsense guidance for safe scale-up and waste disposal. Production-scale handling means thinking ahead: longer transfer lines, batch splitting, solvent choice—all these become part of the manufacturer’s responsibility, not just the end-user’s.

    Many years in the field have taught us that attention to bulk solid flow, ease of transfer, and minimization of static build-up eliminate a lot of downstream headaches. Labeling, traceability, and repack services are standards in our operation because we know even a single drum typically serves several projects.

    Sourcing and Sustainability: The Bigger Picture from Inside the Manufacturer’s Walls

    Sustainable sourcing is no longer an afterthought. Starting materials are tracked and audited, not only for purity but also for environmental compliance. Our procurement team works only with vetted suppliers—to avoid surprise halide levels, unexpected trace metals, or problematic byproducts in the originating fluoro and bromo compounds. We have gradually shifted to greener nitration protocols that generate less nitric acid waste, and we recycle solvents at every feasible opportunity. This is not just policy—it’s a commitment driven by the reality of chemical regulation and the environmental scrutiny we face as direct producers.

    We believe experience-based process modifications, and not just theoretical green chemistry, move the needle toward sustainability. For example, our switch from batch to semi-continuous nitration improved not only environmental performance but also consistency of end-product color and purity. Our waste handling meets both local and international standards, and we routinely invite third-party auditors to validate our claims. These steps come from years of lessons learned—sometimes the hard way—about process safety, regulatory risk, and long-term reputation.

    The direct manufacturer cannot afford shortcuts. Responsible production of compounds like 2-Fluoro-4-Bromonitrobenzene relies on a blend of technical knowledge, practical know-how, and a willingness to improve based on actual use data. Sustainability, transparency, and customer trust are values we’ve developed out of necessity, not marketing.

    Supporting Research and Innovation: Where This Compound Leads Next

    Our involvement in innovation does not end with delivery. Schedule after schedule, researchers approach us looking for adaptation—maybe a modified purification method to suit their downstream solvents, maybe a technical assessment of reaction byproducts unique to their new pathway. Over time, we have collected a deep back-catalog of synthesis knowledge, from ligand and base selection in cross-coupling to practical filtration aids that reduce downtime.

    We share these insights freely because they help everyone. For certain advanced syntheses, where the balance of electron-withdrawing and electron-donating groups matters, use of 2-Fluoro-4-Bromonitrobenzene grants tangible advantages. We don’t generalize this—customers provide feedback, which we review with our internal R&D before suggesting improvements or tweaks. Whether someone is designing a new active ingredient, or testing novel catalysts in material science, we strive to meet practical needs fast and with concrete data.

    Access to the original manufacturing team carries real benefits. If a reaction takes an unexpected direction, we often field calls directly from the bench scientist, not just the purchasing department. We advise on process safety, impurity fate, and even project cost estimates, drawing on our detailed process logs and hands-on production notes.

    Learning from Experience: What Customers Really Want

    Chemists, purchasing managers, and process engineers often ask us for more than just product availability or certificates of analysis. They want reassurance that problems will be solved quickly, and that someone at the producer understands both chemistry and scale-up logistics. Over the years, we’ve supported entire campaign launches, urgent pilot runs, and the trickiest process troubleshooting—all with face-to-face or direct phone support from knowledgeable staff.

    Users working at the pilot stage sometimes need process changes—from custom packaging to adjusted purity specs. We answer these requests transparently. Only accumulated, production-based insight explains why we might adjust crystallization to reduce fines, tweak the particle size for easier suspension, or batch-segment production to fit shifting project priorities. Each adaptation reflects a lesson learned in the field—not just an abstract “service” offering but the daily practice of keeping process chemistry on track.

    Our long-term partners tell us that working with manufacturers, rather than traders or catalog resellers, saves time and reduces risk of disruption. Straight talk, quick samples, and ongoing dialogue come standard. End-users appreciate the difference when a process challenge is met with manufacturer-backed troubleshooting, not just a page from the regulatory binder.

    Regulatory, Logistical, and Export Realities: The Hidden Complexity of Manufacturing Specialty Aromatics

    Logistics and import/export compliance grow more complex every year. As a direct manufacturer, we see up-close how evolving hazardous goods transportation laws, chemical control lists, and customer-specific quality standards shape planning and execution. We maintain detailed compliance packs—not because it is a requirement, but because regulatory landscapes shift fast, especially for halogenated aromatics. Over time, this vigilance has prevented many customer headaches, helping them avoid customs delays, licensing issues, or sudden shifts in labeling needs.

    We coordinate with freight partners, regulatory consultants, and internal documentation teams to stay ahead of changing rules—never assuming last year’s process will work today. Our commitment covers not just product quality at the point of production, but reliability at every link between factory and customer warehouse. Over time, practices like pre-cleared MSDS files, customs declarations tailored for specific export regions, and strong relationships with inspection authorities have set us apart. These steps require investment and detailed planning, but our repeat customers know the value of risk mitigation that only the original manufacturer typically delivers.

    Beyond the Chemical: The Value of Direct Manufacturer Experience

    Many new customers come with stories of delays, unclear technical support, or missing documentation from past suppliers—often those without direct production capabilities. Direct engagement with manufacturers brings more than product—it brings shared accountability, faster troubleshooting, and honest communication about each phase of the supply chain. We welcome plant visits, direct technical audits, and collaborative process reviews. Every feedback cycle strengthens our partnership with users who value more than “commodity” chemistry.

    We see ourselves as an extension of the lab or production team, not just outside vendors. Over the course of thousands of batches, the lessons learned from unplanned shutdowns, successful campaigns, and customer-led process improvements all feed back into how we manufacture 2-Fluoro-4-Bromonitrobenzene. This cycle of listening, adapting, and refining is the real story behind our product.

    Practical experience tells us that, for applied chemistry, the real difference comes not from a catalogue entry or a polished brochure, but from hands-on manufacturing and direct feedback. This is the approach we bring to every customer, every day, with every shipment.