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3-Fluoro-4-Nitrobenzyl Bromide

    • Product Name 3-Fluoro-4-Nitrobenzyl Bromide
    • Alias 3-Fluoro-4-nitrobenzyl bromide
    • Einecs 841-370-4
    • 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
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    Specifications

    HS Code

    318734

    Productname 3-Fluoro-4-Nitrobenzyl Bromide
    Casnumber 60495-60-7
    Molecularformula C7H5BrFNO2
    Molecularweight 234.02
    Appearance Yellow to light brown solid
    Purity Typically ≥98%
    Meltingpoint 48-52°C
    Solubility Slightly soluble in organic solvents (e.g., dichloromethane, chloroform)
    Synonyms α-Bromo-3-fluoro-4-nitrotoluene
    Smiles C1=CC(=C(C=C1Br)F)[N+](=O)[O-]
    Inchi InChI=1S/C7H5BrFNO2/c8-4-5-1-2-7(10(11)12)6(9)3-5/h1-3H,4H2
    Storage Store at 2-8°C, protect from light and moisture

    As an accredited 3-Fluoro-4-Nitrobenzyl Bromide 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 5 grams of 3-Fluoro-4-Nitrobenzyl Bromide, with screw cap and safety labeling for laboratory use.
    Shipping **Shipping Description:** 3-Fluoro-4-Nitrobenzyl Bromide is shipped in tightly sealed, chemical-resistant containers placed within secondary packaging for protection. It is transported with clear hazardous labeling, compliant with local regulations, and shipped at ambient temperature unless otherwise specified by supplier documentation. Appropriate documentation, including safety data sheets and hazard identification, accompanies the shipment.
    Storage 3-Fluoro-4-nitrobenzyl bromide should be stored in a tightly sealed container, away from moisture, light, and incompatible materials such as strong bases and oxidizers. Keep it in a cool, dry, and well-ventilated area, preferably within a chemical fume hood or flammable storage cabinet. Properly label the container and handle with appropriate personal protective equipment to prevent exposure.
    Application of 3-Fluoro-4-Nitrobenzyl Bromide

    Applications of 3-Fluoro-4-Nitrobenzyl Bromide in Industrial Manufacturing

    As a dedicated manufacturer of 3-Fluoro-4-Nitrobenzyl Bromide, we supply this specialty intermediate to a select group of advanced chemical sectors. Below is an overview of established downstream applications, with industry-specific practices and requirements based on our partners’ technical protocols and recent regulatory frameworks.

    1. Active Pharmaceutical Ingredient (API) Intermediate Synthesis

    Pharmaceutical companies utilize this compound in multi-step syntheses for targeted small molecule APIs, particularly in the development of kinase inhibitors and advanced heterocyclic drugs. The fluorinated aromatic ring and functionalized bromo group enable precise regioselective coupling, catering to late-stage intermediate approval in drug pipelines. Manufacturers must meet stringent traceability and impurity profiling demands to maintain registration dossier acceptance.

    Industry compliance standards

    • ICH Q7 GMP for Active Pharmaceutical Ingredients
    • USP, EP, JP monograph specifications (as applicable to final API)
    • Pharmaceutical cGMP auditing standards
    • REACH Registration (for EU-supplied substances)

    Typical usage ratio

    • 0.25–1.5 molar equivalents, with precise adjustment based on coupling efficiency and desired impurity ceiling per batch process

    Downstream process integration

    • Introduced at the nucleophilic aromatic substitution or alkylation step, typically following hydrogenation or nitration, then processed further into heterocycle formation or amide linkage applications

    Final product types

    • Small molecule oncology APIs (e.g., novel kinase inhibitors)
    • Anti-inflammatory drug intermediates
    • Late-stage pharmaceutical intermediates destined for clinical development

    2. Agrochemical Active Component Intermediate

    Major agrochemical formulators incorporate our compound as a precursor in the synthesis of fluorinated phenyl-based active ingredients for insecticides and select herbicides. The nitro and bromo substitution confers desirable metabolic stability during subsequent arylation or amination steps, assisting manufacturers in meeting residue and environmental fate targets mandated by regulatory authorities.

    Industry compliance standards

    • FAO/WHO Joint Meeting on Pesticide Specifications (JMPS)
    • ISO 9001:2015 QMS for crop protection ingredient synthesis
    • OECD Guidelines for the Testing of Chemicals
    • National Registration Authorities (EPA, ECHA BPR, etc.)

    Typical usage ratio

    • 0.2–1.0 mole per target synthetic conversion, depending on downstream coupling yield and impurity control thresholds set by product registration dossiers

    Downstream process integration

    • Deployed in the preparation of substituted phenyl rings prior to esterification or amidation, or as a key step in building fused-ring pesticide cores

    Final product types

    • Fungicide and insecticide active substances with fluorinated aromatic nuclei
    • Pre-mix intermediates for selective herbicide payloads

    3. Custom Synthesis for Advanced Organic Electronic Materials

    Electronic materials developers employ this compound as an essential building block in the custom synthesis of fluorinated monomers and organic small molecules for OLED emitters, organic semiconductors, and sensor substrates. The compound’s functionalization pattern supports high-purity coupling, crucial for optical and electronic performance, requiring careful inventory control in ISO-certified production lines.

    Industry compliance standards

    • ISO 9001:2015 Quality Management Systems for electronic material production
    • RoHS 3 (EU Directive 2015/863) for use in device components
    • Reach SVHC screening relevant to precursor substances
    • Customer-dictated trace impurities limit (often <100 ppm)

    Typical usage ratio

    • 0.1–0.6 mole per custom monomer batch, modulated according to required electron transport and optical purity parameters

    Downstream process integration

    • Input for the aromatic substitution or Suzuki coupling stage before polymerization, typically processed under inert atmosphere and low-metal catalyst conditions to meet electronic-grade yield

    Final product types

    • OLED blue-green emitter intermediates
    • Fluorinated semiconducting monomers for OFET devices
    • Optoelectronic sensor material constituents

    4. Specialty Dye and Pigment Precursor Synthesis

    Specialty dye manufacturers select this compound for the stepwise construction of novel nitroaromatic and fluoroaromatic dyes used in textile coloration, security inks, and high-performance pigments. The molecular features enable direct participation in chromophore extension reactions, supporting high color strength and stability requirements for commercial formulation partners.

    Industry compliance standards

    • OEKO-TEX Standard 100 for restricted aromatic amines in dyes
    • ISO 14001 Environmental Management (for pigment and dye manufacturing sites)
    • EU REACH Annex XVII restricted substances list
    • GHS SDS and CLP compliance for trade and downstream shipment

    Typical usage ratio

    • 0.3–1.2 mole per chromophore build sequence, ratio determined by targeted color index structure and desired shade intensity

    Downstream process integration

    • Added during the initial aromatic substitution stage for azo or anthraquinone dye construction, then subjected to diazotization or condensation with coupling components

    Final product types

    • Nitroaromatic textile dyestuffs
    • Fluorinated pigments for industrial coatings
    • Anti-counterfeiting security inks with specific fluorescence spectra
    Free Quote

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    Certification & Compliance
    More Introduction

    3-Fluoro-4-Nitrobenzyl Bromide: Purpose-Built for Advanced Synthesis

    Crafting 3-Fluoro-4-Nitrobenzyl Bromide with Precision and Expertise

    In the fine chemical industry, quality and control start long before a bottle reaches the customer. Manufacturing 3-Fluoro-4-Nitrobenzyl Bromide has shown us the value of careful process development and strict analytical checks. The compound itself, 1-bromo-3-fluoro-4-nitrobenzyl, emerges from a blend of selective halogenation and nitration, designed for functionality that supports advanced organic synthesis. Chemists looking for a distinctive benzyl halide with both electron-withdrawing and electron-donating features often focus on this molecule because of its reactivity pattern, unique functional groups, and the doors it opens in pharmaceutical and agrochemical development. The product’s clear utility isn’t just theoretical—it’s seen on benches and in reactors where reliable building blocks drive new discoveries.

    Why Choose Our Manufactured 3-Fluoro-4-Nitrobenzyl Bromide?

    Producing this compound is not about simply following a recipe. Our chemical engineers and lab teams have spent hundreds of hours fine-tuning the route to obtain a pure, stable product free from troublesome by-products like dibromides or dehalogenated species. That’s the distinction between a lab curiosity and a reliable industrial input. We control starting materials stringently, from fluorinated anilines to the exact source and strength of our brominating agent. Our approach leverages process safety and consistent yield, because unpredictable impurities can quickly wreck a multi-step synthesis or damage sensitive catalyst systems downstream. Years of manufacturing experience have underscored the importance of reproducibility, especially when customers are developing active pharmaceutical ingredients or exploring structure-activity relationships in medicinal chemistry.

    Specifications that Matter in Real-World Applications

    Buying fine chemicals shouldn’t be a gamble on batch-to-batch consistency. Ask anyone in the industry—every minor impurity signals trouble ahead. Our 3-Fluoro-4-Nitrobenzyl Bromide consistently delivers a minimum purity of 98% by GC analysis, based on repeated, independent lot testing. Each manufactured batch matches the requirement for limited moisture and manageable color, essential for predictable reactivity. Melting point, density, and halide content match technical literature within tight ranges, so formulation chemists and organic researchers know precisely what to expect. Scale is always matched to customer need, from gram-amounts for new methods to multi-kilo batches for process validation. These aren’t textbook values, but the outcome of hands-on troubleshooting and real production runs.

    Comparing to Other Benzyl Bromides—A Practitioner’s Viewpoint

    Some customers ask, why this compound rather than a standard benzyl bromide or simple fluoro-substituted alternatives? The fluorine at the ortho-position and nitro at the para-position bring marked differences in reactivity. The electron-withdrawing nitro group enables certain nucleophilic reactions that traditional benzyl bromides don’t support well. The presence of fluorine tweaks the molecule’s reactivity profile, impacting rates of alkylation or influencing selectivity in cross-coupling reactions. Compared to mono-nitro or unsubstituted variants, this version stands out when specific synthetic transformations are required—for example, when a strong para-electron withdrawing effect is needed to stabilize intermediates or facilitate downstream substitution. We have witnessed countless research labs achieve smoother transformations because unwanted side reactions, so common with less complex benzyl bromides, occur less with this molecule’s well-chosen substitutions. The result is often cleaner reactions, fewer purification headaches, and better yields.

    How Our Experience Improves Outcomes

    Problems rarely announce themselves politely in chemical manufacturing. Over the years, we recognized that controlling ambient humidity, reaction exotherms, and purification conditions is crucial to consistent outcomes. Our facilities use closed-system reactors under inert nitrogen, always monitored for pressure spikes and temperature drifts. For this product, temperature profiles have a direct effect on electrophilic substitution and side-product formation. Our approach adjusts stirring speed, order of addition, and time at key stages, because we have learned from experience that neglecting any detail multiplies risk. Early on, a single unchecked variable ruined plenty of product in pilot runs. Now, we document every deviation and track process analytics batch-by-batch.

    Our technical support comes from years on the factory floor and in the lab, not just from instructions on a data sheet. Chemists in pharma and materials research often ask for advice on storage, quenching, or solvent compatibility. Because we handle this product in bulk, we’ve seen how solvent residuals, timeline delays, or temperature excursions play out. We don’t guess at stability; every packaged lot is tested post-manufacture. Our recommendations for dry, sealed storage—preferably under argon or nitrogen—stem from empirical studies showing minimized byproduct formation and color changes. For users with automated synthesis platforms, we provide guidance on pump and seal compatibility, based on real-world failures observed and resolved in our own systems.

    Performance in Real Synthesis

    Academic papers rarely capture the frustration a chemist feels when a batch doesn’t perform as expected. For 3-Fluoro-4-Nitrobenzyl Bromide, success depends on solid preparation. We tackled the difficulties of hydrolysis and competitive substitution that can plague halogenated benzyls, so customers receive a product ready for direct use in Williamson ether syntheses, nucleophilic aromatic substitution, and cross-coupling. Our R&D teams have worked on scaled applications, including the synthesis of fluorinated aromatic drugs, spiropyran materials, and various aryl ether intermediates used in agrochemical discovery. Some partners use our product in high-throughput screenings, benefiting from its elevated purity—fewer false negatives translate to more robust SAR data and less wasted effort downstream.

    Over time, we have refined drying protocols and packaging solutions by assessing long-term trending data. Early failures gave us lessons in managing moisture traps, trace contaminants, and even glassware passivation. Chemists using our material receive documentation and advice rooted in practical troubleshooting, and that saves them weeks chasing down avoidable process issues. Reports from the field prove that reproducibility remains high when best practices are observed—proof that process knowledge trumps generic handling guides every time.

    Understanding the True Value in a Specialty Chemical

    Most benzyl halides in catalogs originate from basic halogenations using typical conditions and raw materials. We approached the synthesis of 3-Fluoro-4-Nitrobenzyl Bromide differently, focusing on phase transfer techniques, advanced halogen donors, and highly selective nitration steps to minimize formation of regioisomers. Experience taught us that even tiny percentages of ortho, meta, or polynitro byproducts will ruin the downstream chemistry with sensitive catalysts or precision reagents. Regular monitoring by NMR and HPLC, not just bulk GC, flags any deviation in real time and allows us to intervene before an impurity becomes expensive waste. Each improvement, from refining filtration protocols to realigning purification methods, reflects real production challenges our teams have solved in practice.

    In the early days, we saw firsthand how many issues arise on scale-up, not during lab-scale pilot trials. Factors like agitator design or trace heavy metals from process equipment can influence a batch’s outcome. Continuous improvement pushes us to review every raw material source, check for batch-to-batch color consistency, and upgrade containment systems. The result is stable quality and improved environmental performance, which in turn supports more predictable research and manufacturing for end users.

    Supporting Informed Choice in Sourcing

    Direct communication between manufacturer and customer matters most when unusual requirements or new synthetic routes emerge. Many of our best process enhancements started from a conversation with a client facing an unexpected problem—like interference from a stabilizer in long-term storage, or solubility challenges in specific solvents like DMSO or DMF. As a manufacturer, we can tailor solutions, not just sell a standard bottle off the shelf. Feedback drives us to explore alternate grades, customized to the requirements of emerging applications, whether for small-scale medicinal chemistry or pilot-plant validation.

    The practical aspects of handling 3-Fluoro-4-Nitrobenzyl Bromide in a working lab environment are never far from our minds. Advice on dispensing, minimizing airborne particulate, and appropriate PPE all trace back to hands-on use—not just from reading MSDS sheets. A blend of respect for safety and deep familiarity with the compound’s quirks allows our technical team to deliver guidance that keeps customers productive and safe. Over years, we have seen recurring issues: glassware residue buildup, operator error during transfer, or early onset of slight yellowing signaling slow decomposition. These aren’t abstract risks or over-cautious regulatory warnings—they come straight from our own operations and form the backbone of our technical recommendations.

    Differentiation: What Sets This Material Apart

    Among benzyl bromides, several key differences define the niche for 3-Fluoro-4-Nitrobenzyl Bromide. Classic benzyl bromides often disappoint in modern medicinal chemistry because their simple reactivity profile yields poor selectivity in functional group-rich environments. The 3-fluoro and 4-nitro combination, in contrast, modulates the activation of the aromatic ring, leading to meaningful changes in substitution patterns and product profiles. Many researchers have noted improved yields in their target compounds and reduced need for chromatographic purification thanks to fewer side reactions and cleaner reaction plates.

    This difference shows up most sharply in advanced heterocycle synthesis, custom alkylation steps, and processes where regioselectivity or functional group tolerance are critical. We’ve seen time-sensitive projects recover lost weeks thanks to a cleaner reaction enabled by the right substrate choice. Every differential performance, measured against related bromides or even chloride analogs, has come from careful attention to detail at the manufacturing stage—control of byproduct formation, fresh purification solvents, and contamination-free handling conditions.

    Our Commitment to Ethical Sourcing and Environmental Responsibility

    Sustainable manufacturing isn’t just talk for us. We build our production on high-purity fluorinated building blocks sourced from trusted partners who share our standards for traceability and environmental stewardship. Waste treatment systems, rigorous emissions controls, and regular audits keep us accountable. Our synthetic route was selected with waste minimization in mind; halogenated byproducts are captured, recycled, or disposed of according to stringent standards. Each batch can be traced from raw material sourcing through production and delivery—a necessity, not a luxury, in today’s regulatory landscape. Staying out front with new environmental guidelines and continual process optimization is a central part of our daily work, not an occasional check-box exercise.

    We recognize that supporting our customers’ compliance requirements means more than just paperwork. When new documentation or deeper batch-specific analytics become essential for regulatory filings or ISO compliance, our teams respond promptly and thoroughly. Our investment in analytical technology, traceable recordkeeping, and intensive process QA helps maintain the standard researchers and industry partners can stake their outcomes on.

    Investing in Knowledge and Customer Success

    Shaping a reliable, useful specialty chemical out of a complex synthetic pathway depends on a lot more than a simple process flow. We invest constantly in analytical resources—not just routine purity checks, but advanced techniques like high field NMR and ICP-MS when the application calls for it. By training our staff and staying engaged with the front lines of chemical development, we keep our perspective sharp and relevant. That’s helped us spot trends early, such as increased demand for high-purity aromatic building blocks in new drug discovery platforms, and the need for faster, more detailed documentation to support regulatory filings worldwide.

    Our product specialists routinely troubleshoot synthesis challenges side-by-side with customer teams. We encourage open dialogue about issues, whether those are reactivity mismatches, unexpected byproducts, or mundane packaging needs. Each successful project expands our practical playbook—benefiting future customers and streamlining new product roll-outs. Experience proves that a direct line to the manufacturer saves time and prevents the small disasters that can follow afterthought sourcing or commodity purchasing. Partnering with experienced chemical manufacturers enables your goals, whether speeding a lead compound to clinical trials or optimizing a high-throughput screening campaign.

    Looking Ahead: The Role of Reliable Benzyl Halides in Innovation

    Complex synthesis will keep demanding smarter building blocks and unwavering purity. Researchers exploring new catalysts, functionalized polymers, or bioactive compounds can’t afford delays from unpredictable supply or substandard materials. Our focus on continuous process improvement—based on data, not wishful thinking—ensures each gram of 3-Fluoro-4-Nitrobenzyl Bromide contributes to project success. We stay ready to refine, adapt, and scale in response to new synthetic challenges. Recognizing the stakes involved, from project deadlines to compliance with evolving regulatory standards, keeps us engaged with every batch. The results speak for themselves in day-to-day laboratory use, successful project scale-ups, and the trust clients place in direct manufacturing partnerships.

    For users who need a specialty halide that brings reliability and smart reactivity to their synthesis, direct sourcing from a manufacturer with expertise, transparency, and robust processes often makes all the difference. Our commitment extends well beyond product delivery—grounded in the hands-on experience of chemists and engineers dedicated to doing the job right, every step from raw material selection to end-user support.