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4-Bromo-5-Fluoro-2-Nitrotoluene

    • Product Name 4-Bromo-5-Fluoro-2-Nitrotoluene
    • Alias 4-Bromo-5-fluoro-2-methyl-1-nitrobenzene
    • Einecs 843-730-7
    • 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

    632276

    Chemical Name 4-Bromo-5-Fluoro-2-Nitrotoluene
    Molecular Formula C7H5BrFNO2
    Cas Number 1171419-06-9
    Appearance Yellow solid
    Smiles CC1=CC(=C(C=C1Br)F)[N+](=O)[O-]
    Inchi InChI=1S/C7H5BrFNO2/c1-4-2-5(8)7(9)6(3-4)10(11)12/h2-3H,1H3

    As an accredited 4-Bromo-5-Fluoro-2-Nitrotoluene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing A sealed amber glass bottle containing 25 grams of 4-Bromo-5-Fluoro-2-Nitrotoluene, clearly labeled with safety and hazard information.
    Shipping 4-Bromo-5-Fluoro-2-Nitrotoluene is shipped in tightly sealed, chemical-resistant containers, compliant with international and domestic hazardous material regulations. It is transported under controlled conditions, protected from heat and moisture, and accompanied by proper documentation, including Safety Data Sheets (SDS). Handle with care to avoid exposure, spills, or environmental release during shipping.
    Storage 4-Bromo-5-Fluoro-2-Nitrotoluene should be stored in a tightly closed container, in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible materials such as strong oxidizing agents and bases. Keep out of direct sunlight and protect from moisture. Ensure proper labeling and use appropriate personal protective equipment when handling the chemical.
    Application of 4-Bromo-5-Fluoro-2-Nitrotoluene

    Applications of 4-Bromo-5-Fluoro-2-Nitrotoluene in Industrial Manufacturing

    4-Bromo-5-fluoro-2-nitrotoluene is a specialized halogenated aromatic intermediate, primarily integrated into value chains that require advanced chemical building blocks for the synthesis of pharmaceuticals and agrochemicals. As a manufacturer, we supply this intermediate for select downstream sectors, where precise regulatory adherence, dedicated process controls, and formulation consistency are required for market authorization and batch reproducibility. Below, we detail typical real-world application scenarios across several sectors, highlighting compliance standards, usage ratios, process inlets, and final product forms shaped by technical and industrial needs.

    1. Pharmaceutical Active Pharmaceutical Ingredient (API) Intermediate Synthesis

    Innovators and generic API manufacturers depend on 4-bromo-5-fluoro-2-nitrotoluene as a key reagent during the multi-step synthesis of heterocyclic core structures for novel or patent-expired active pharmaceutical compounds. The halogen and nitro functionalities offer reactivity required for selective coupling, halogen-metal exchange, and nucleophilic substitution strategies, facilitating the construction of benzo-fused frameworks for anti-infective, CNS-active, and oncology small molecules.

    Industry compliance standards

    • Current Good Manufacturing Practice (cGMP) – ICH Q7, FDA 21 CFR Part 210/211
    • Pharmacopeial reference standards – USP-NF, EP, JP as required per API
    • ISO 9001:2015 Quality Management for intermediate control
    • REACH (EC) No 1907/2006 registration for substance safety

    Typical usage ratio

    • Intermediate loading typically at 0.85–1.8 molar equivalent per synthetic step; ratio set by target API structure and throughput requirements, phased in the initial or second coupling stage.

    Downstream process integration

    • Reactant input in palladium-catalyzed cross-coupling or halogen-metal exchange (e.g., Suzuki, Buchwald, or Grignard reactions) for assembling biaryl or heterocyclic linkages during the API’s core skeleton synthesis.

    Final product types

    • Final APIs including substituted benzothiazoles, fluorinated anilines, or nitroaromatics for branded or generic pharms, such as CNS drugs, antimicrobials, and kinase inhibitors.

    2. Agrochemical Active Compound Synthesis

    Agrochemical manufacturers employ 4-bromo-5-fluoro-2-nitrotoluene as a halogenated precursor in synthesizing novel herbicide and pesticide actives. Its unique substitution pattern supports structure-activity relationship (SAR) optimization, enabling downstream synthesis of fluorinated heterocycles known for persistence in plant protection products.

    Industry compliance standards

    • FAO/WHO specifications for technical materials and active ingredients
    • ISO 9001:2015 for agrochemical intermediate handling
    • EU Regulation (EC) No 1107/2009 for placing plant protection products on the market
    • China GB 38502-2020 for chemical pesticide technical

    Typical usage ratio

    • Employed at 1.0–1.25 molar equivalent depending on target actives, such as triazole, pyrazole, or benzoxazole derivatives, introduced at the heterocycle-building step.

    Downstream process integration

    • Added during aromatic halide substitution or nucleophilic aromatic substitution (SNAr), followed by cyclization or rearrangement for creating bioactive heterocycles.

    Final product types

    • Crop protection actives: fluorinated triazoles, nitroaromatic pesticides, and herbicide intermediates incorporated into finished emulsifiable concentrates (EC), suspension concentrates (SC), or wettable powders (WP).

    3. Specialty Chemical Intermediates for Advanced Polymer Synthesis

    Polymer manufacturers incorporate this aromatic intermediate within specialty monomer manufacturing, where its electron-withdrawing substituents modulate polymer backbone stability and functionality. The bromo and fluoro groups support introduction of polar and reactive moieties for custom performance materials used in coatings, high-dielectric resins, or electronics encapsulants.

    Industry compliance standards

    • ISO 9001:2015 for specialty chemical manufacturing
    • RoHS (Restriction of Hazardous Substances) for electronics-related polymers
    • REACH (EC) No 1907/2006 for polymers and monomer safety
    • GHS labeling and hazard communication (UN, OSHA, EU-CLP)

    Typical usage ratio

    • Intermediate charged at 0.65–1.5 molar per monomer, tuned relative to backbone design, polymer chain length, and targeted end-use property such as dielectric strength or chemical resistance.

    Downstream process integration

    • Functionalized monomer synthesis (amide, ether, or sulfone linkers), with subsequent step-growth or chain polymerization into pre-polymers, cured resins, or copolymers for advanced materials.

    Final product types

    • High-reliability encapsulants, chemically resistant coatings, electronics-grade potting compounds, and performance adhesives.

    4. Fine Chemical Synthesis for Dye and Pigment Precursors

    In colorant manufacturing, this intermediate acts as a building block for synthesizing functional dye intermediates, especially for high-performance pigments with enhanced substrate affinity or thermal resistance. Its halogen positioning enables targeted electrophilic or nucleophilic modifications, used in dyestuff synthesis workflows for textiles, plastics, and coatings.

    Industry compliance standards

    • Oeko-Tex Standard 100 – Textile and ecological standards
    • ISO 9001:2015 for dye and pigment supply chains
    • EU REACH – Registration for dye intermediates
    • ZDHC MRSL – Limits for hazardous chemical inputs in textiles

    Typical usage ratio

    • Inserted at 0.3–1.1 equivalents based on targeted pigment ring structures and degree of functionalization required by the downstream chromophore.

    Downstream process integration

    • Bromination-activated coupling or nitration/fusion to assemble azo, anthraquinone, or phthalocyanine dye intermediates ahead of final colorant synthesis and post-treatment steps.

    Final product types

    • Textile disperse dyes, inkjet pigment dispersions, heat-stable plastics colorants, and specialty pigment concentrates for coatings.
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    Certification & Compliance
    More Introduction

    4-Bromo-5-Fluoro-2-Nitrotoluene: A Closer Look at Our Manufacturing Process and Its Role in Advanced Synthesis

    Introduction to 4-Bromo-5-Fluoro-2-Nitrotoluene

    Aromatics have a longstanding reputation in the fine chemical industry for their versatility and reliability. Among the substituted toluenes, 4-Bromo-5-Fluoro-2-Nitrotoluene offers unique properties and advantages, especially for customers involved in pharmaceutical research, agrochemical design, and advanced material science. We have been manufacturing this compound for several years, continuously refining our process for consistent quality and safe handling. This page focuses on in-house experience, pragmatic observation, and the value this molecule brings to end users who expect traceability and batch-to-batch consistency.

    Model, Specifications, and Physical Characteristics

    Our 4-Bromo-5-Fluoro-2-Nitrotoluene bears the molecular formula C7H5BrFNO2. Production follows a controlled sequence of selective bromination and fluorination, integrating robust nitration technology. Over multiple campaigns, we've found optimal conditions that minimize byproduct formation and enhance yield so each batch meets customer assay needs for high purity, low residual solvent, and defined impurity profile. Physical form manifests as a pale-yellow crystalline powder, with melting points typically between 54 and 58°C. Purity routinely tests at ≥98% by HPLC. Water content and residual solvents also undergo monitoring. Each shipment includes a full certificate of analysis, traceable back to the starting materials.

    Packing standards rely on customer feedback; most request sealed fiber drums lined with polyethylene to avoid moisture uptake during overseas shipment. Those with small-lot laboratory needs ask for bottles purged with inert gas, a setup our technical team introduced after an incident involving slow hydrolysis by ambient humidity. Storage requirements are straightforward—keep the drum tightly sealed, in a dry, well-ventilated place, at room temperature away from strong acids or bases.

    Application: Why Synthetic Chemists Value This Compound

    We have watched the demand profile for 4-Bromo-5-Fluoro-2-Nitrotoluene shift over the years as discovery teams look for building blocks with specific substitution patterns. The dual halogenation at the para and meta positions grants greater molecular diversity, especially when constructing active pharmaceutical ingredients (APIs) with complex arene substitution. The nitro group sits ortho to the methyl, and this arrangement lays the groundwork for efficient nucleophilic aromatic substitution, cross-coupling reactions, and reduction chemistry.

    Our partners in medicinal chemistry find this pattern valuable because it enables late-stage functionalization. The bromine and fluorine serve as handles for Suzuki or Buchwald-Hartwig coupling, while the nitro component can be reduced to an amine or transformed into other useful intermediates. Researchers developing new fungicides have incorporated this scaffold as a key synthon, reporting enhanced biological activity due to the combined electron-withdrawing influences. Fluorination patterns like this are hard to install by post-synthetic modification; supplying it directly allows customers to skip several steps, improving throughput and lowering total costs.

    Differences from Other Substituted Aromatics

    It’s easy to overlook the impact of subtle substitutions on reactivity, especially when comparing to its close relatives such as 4-Bromo-2-nitrotoluene or 5-Fluoro-2-nitrotoluene. By manufacturing several related compounds ourselves, we have firsthand knowledge of how the position of bromine and fluorine markedly alters both chemical behavior and physical properties. For instance, 4-Bromo-5-Fluoro-2-Nitrotoluene displays higher resistance to oxidative degradation than mono-halogenated analogs, improving shelf life under non-ideal storage conditions.

    Chemists using mono-halogenated nitrotoluenes often report diminished cross-coupling efficiency when scaling up, since their single reactive leaving group limits flexibility. Having both bromine and fluorine unlocks more options for functionalization. Compared to 2,6-difluoro-4-nitrotoluene, ours offers easier isolation and purification in downstream chemistry; the bulkier bromine atom draws out different selectivity in many common reactions. Customers have told us how their old syntheses that used non-ortho substituted nitrotoluenes needed more purification, extra chromatographic steps, and sometimes resulted in persistent impurities. Our product’s regiochemistry solves these problems by making reaction monitoring and purification more predictable.

    Environmental and safety aspects differentiate this compound from more reactive or highly toxic alternatives. Although we instruct users to avoid skin and inhalation exposure, the hazard profile compares favorably to more volatile compounds bearing multiple nitro or halogen groups. Routine plant audits and years of safe operation suggest a manageable risk profile under best-practice handling procedures, especially with closed transfer equipment and local exhaust ventilation.

    Comparison Based on Field Experience

    Feedback from process chemists and scale-up managers carries the most weight for us, since they encounter problems beyond what lab-scale suppliers anticipate. Some have tried importing similar materials from other regions, only to run into issues with stability, solubility, or unpredictable assay results. Our repeated investments in process control and monitoring ensure reproducibility, leading to fewer deviation reports and smoother regulatory filings.

    Regular contact with people scaling up advanced intermediates has taught us how reaction exotherm, gas evolution, or crystallization kinetics can make or break a campaign—details that background literature seldom covers. For example, in palladium-catalyzed couplings, we’ve seen how our tightly controlled impurity spectrum delivers more robust filtration and workup, reducing downtime and unplanned cleaning cycles for large vessels.

    Formulators developing new chemical entities often examine side reaction profiles under a variety of conditions. Customer labs have shared analytical reports showing that our 4-Bromo-5-Fluoro-2-Nitrotoluene exhibits fewer side reactions in both reduction and substitution conditions, compared to similar products from non-integrated suppliers. Since we control each step from starting material to packaged product on-site, this quality advantage emerges naturally. We do not blend or repackage materials from outside—every gram comes off our own lines, under the technicians’ supervision familiar with each batch’s history.

    Manufacturing Practice and Technical Commitment

    Years spent refining each process step taught us that reproducibility hinges not only on equipment and control, but on the know-how of the people running the plant. Early on, we focused on minimal waste, safe temperature profiles, and clear documentation for each reactor run. For reagents like fluorinating agents, hazards run higher than most aryl brominations; over time, careful staff training and ongoing hazard reviews have made our production line safer and more productive. All lots receive final inspection in-house, with detailed spectral libraries built for each batch. Over more than a decade, internal standards for appearance, melting point, and chromatographic fingerprinting have evolved alongside advances in analytical chemistry.

    Every specification—purity, isomeric composition, residual halides—ties back to tangible process improvements. Instead of introducing variations with each scale-up, our team’s familiarity with the reaction’s critical parameters helps ensure that even when a new lot number is assigned, the analytical chemist can link every measurement back to the right tank or reactor. This reduces both customer troubleshooting and our internal cycle time between contract orders.

    Supporting Innovations in Research

    We notice that high-throughput screening platforms now rely on denser libraries of functionalized arenes, especially those bearing combinations of nitro, halogen, and methyl groups. As research cycles get shorter, chemists turn to commercial suppliers for access to rare or hard-to-install patterns. Each year, our customers synthesize more candidates with fluorinated aromatic cores, in hopes of improving metabolic stability or gaining novel structure-activity relationships.

    The economic importance of being able to introduce two halogen atoms and one nitro group in a single molecule, securely and reproducibly, cannot be overstated from a chemistry perspective. By controlling the entire route in-house, and optimizing safety protocols for both routine and abnormal situations, we ensure reliable supply to development teams under demanding timelines. Resources spent on rework or secondary purification shrink when starting material quality remains high. Large-scale production, direct from manufacturer, gives customers a line of sight into supply chain security—they track origin, identify critical control points, and request changes as needs evolve, without dealing with the black box of resellers or repackers.

    Practical Considerations and Troubleshooting

    Seasoned chemists know how batch-to-batch variation derails lab timelines or plant operations. From the earliest days of producing this molecule, we’ve seen the impact of close technical support: researchers rely not just on assay numbers from a report, but on practical guidance for handling, dissolution, and purification. Technical discussions sometimes reveal incompatibilities with certain solvents or process steps that competitors might overlook. By running comparative internal tests, we identify solvent choices that maximize yield and selectivity, and share tips with our customers about how to get the cleanest possible reaction profiles. This means fewer surprises on a chemist’s bench or in a kilo-scale reactor when making the first crucial intermediates for a new API or agrochemical.

    Sometimes customers try to source 4-Bromo-5-Fluoro-2-Nitrotoluene from generic online catalogs and find themselves dealing with unpredictable solids, color changes, or unidentified impurities. Our on-site QC lab documents every out-of-spec sample and shares findings transparently. These measurements often catch impurities just tall enough to evade typical spot checks but harmful in downstream coupling steps. We update analytical certificates after every production run, and encourage customer feedback via direct technical consultation—this feedback loop has improved not only our in-house specifications but also customers’ operational reliability. By staying close to the true manufacturing process, we sidestep “unknown unknowns” that grow when products pass through too many hands.

    Supply Assurance and Sustainable Practice

    A dependable supply of key building blocks underpins progress in the pharmaceutical, materials, and agrochemical sectors. Recent disruptions in global logistics highlighted the difference between direct manufacturers and resellers. We draw on decades of experience navigating raw material shortages, changing regulations, and new environmental demands. Our facility routinely invests in emission controls, solvent recycling, and responsible waste treatment—not because these changes look good in a brochure, but because operational discipline reduces risk of shutdown and ensures contracts stay fulfilled. Engineers installing upgraded separation columns last year relied not on abstract green standards, but on hard-won knowledge of effluent volumes, solvent streams, and reactivity profiles.

    Reliable access to building blocks like 4-Bromo-5-Fluoro-2-Nitrotoluene depends on stability not only in supply chain operations, but in technical mastery. Instead of seeking quick shortcuts or chasing low-margin markets, we focus on mastering each production detail—an approach that comes from years of navigating real-world setbacks and learning from each campaign. Product stewardship shapes every interaction with customers, regulators, and our own team, fostering resilience amid a climate of uncertainty.

    End-User Dialogue and Innovation Partnership

    Chemistry does not stand still, and neither do the needs of active researchers. Regular dialogue with end users keeps us aware of pain points, such as need for microscale vials for lead optimization, or cleaner impurity profiles to satisfy new regulatory review. Feedback has pushed us beyond simple scale-up: we now offer tailored packs for R&D, custom impurity benchmarking, and can even accommodate special analytical testing upon request. Our approach values transparency—customers increasingly want to know not only specs but details of synthetic route, environmental impact, and scalability. By fostering open technical exchange, we create room for collaboration and rapid troubleshooting on the ground.

    No innovation emerges in isolation. As researchers introduce new catalyst systems or probe more challenging functionalizations, our in-house technical team explores new derivatization possibilities for arene building blocks. Investing in upstream R&D means not only anticipating tomorrow’s specification, but actively supporting those pushing the boundaries of synthetic organic chemistry.

    Looking Forward: Integrity and Reliability in Chemical Manufacturing

    At the manufacturing level, 4-Bromo-5-Fluoro-2-Nitrotoluene is much more than a line item in a catalog. It represents the outcome of careful process design, practical chemical engineering, and steady refinement based on direct user experience. The subtle interplay of reagent choice, scale-up logistics, plant safety, and application support all play a part in the product's real-world impact.

    By controlling every step of production—sourcing, synthesis, isolation, finishing, and quality verification—we offer users more than a material; we offer consistency, predictability, and technical partnership. These are not abstract promises but the result of tried-and-tested routines established by teams who understand the consequences of every reaction step, every packaging detail, every analytical run.

    Ongoing engagement with research partners, open communication regarding specifications, and an unwavering commitment to safe and efficient operations underscore every lot that leaves our facility. We see the value our work brings to innovation, not only in the purity of a crystalline powder, but in the trust that customers place in us as a manufacturer. The future of advanced chemical synthesis depends on reliability at every level—from molecule to finished product—and we strive to maintain that standard, day in and day out.