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1-Bromo-2-Fluoro-4-Nitrobenzene

    • Product Name 1-Bromo-2-Fluoro-4-Nitrobenzene
    • Alias 1-Bromo-2-fluoro-4-nitrobenzene
    • Einecs 809-090-1
    • 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

    905240

    Iupac Name 1-Bromo-2-fluoro-4-nitrobenzene
    Molecular Formula C6H3BrFNO2
    Molecular Weight 220.00 g/mol
    Cas Number 446-09-3
    Appearance Yellow to light brown solid
    Melting Point 50-54°C
    Boiling Point 249-251°C
    Density 1.75 g/cm³
    Refractive Index 1.587 (at 20°C)
    Solubility In Water Insoluble
    Flash Point 107°C
    Smiles C1=CC(=C(C=C1Br)F)[N+](=O)[O-]

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

    Packing & Storage
    Packing Brown glass bottle, 100g, sealed with a plastic screw cap. Label displays chemical name, formula, warnings, and supplier details.
    Shipping 1-Bromo-2-Fluoro-4-Nitrobenzene is shipped in tightly sealed containers, protected from light, moisture, and physical damage. It must comply with hazardous material transport regulations, clearly labeled as a toxic and irritant chemical. Shipment requires secure outer packaging and documentation per international and local guidelines to ensure safe handling and delivery.
    Storage Store 1-Bromo-2-Fluoro-4-Nitrobenzene in a cool, dry, well-ventilated area away from heat, sparks, and incompatible materials such as strong reducing agents. Keep the container tightly closed, protected from light and moisture. Use appropriate, chemical-resistant containers and ensure proper labeling. Wear suitable protective equipment when handling, and follow all safety guidelines for hazardous and potentially toxic chemicals.
    Application of 1-Bromo-2-Fluoro-4-Nitrobenzene

    Applications of 1-Bromo-2-Fluoro-4-Nitrobenzene in Industrial Manufacturing

    As a direct manufacturer of 1-Bromo-2-Fluoro-4-Nitrobenzene with established technical expertise, we support specialized industries with this high-purity intermediate designed for demanding synthesis environments. Our material serves as a valuable building block in sectors requiring stringent compliance, precise dosing, and reproducible performance across advanced downstream processes. Listed below are the primary industrial application fields where this compound reliably advances production outcomes for our clients.

    1. Agrochemical Active Ingredient Synthesis

    Producers of selective herbicides and advanced fungicides use 1-Bromo-2-Fluoro-4-Nitrobenzene as a nucleophilic aromatic intermediate in multistep manufacturing of fluorinated agrochemicals. Its ortho-bromo and para-nitro configuration enables high-yield coupling and substitution reactions under controlled catalytic conditions, fitting within regulated synthetic routes to ensure molecule integrity required for crop protection applications.

    Industry compliance standards

    • ISO 9001:2015 Quality Management Systems
    • CropLife International stewardship criteria
    • REACH Registration (EU No. 1907/2006 for import and use)
    • Globally Harmonized System (GHS) for labeling and handling

    Typical usage ratio

    • Applied at 0.2 – 0.9 molar eq. per key synthesis step, relative to target ring precursors—final addition rates optimized for reaction completeness and minimal by-product generation based on herbicide or fungicide formula specifications.

    Downstream process integration

    • Charged into aromatic halogen exchange or nucleophilic substitution reactors after substrate activation; often introduced during mono- or di-fluoroaryl aniline synthesis before cyclization, with full traceability from batch weighing onward.

    Final product types

    • Systemic herbicide active technical concentrates
    • Contact fungicide intermediates
    • Pre-emergence weed control agents
    • Granule/powder formulations for direct farm application

    2. Pharmaceutical Intermediate Manufacturing

    Leading pharmaceutical manufacturers select our material for the creation of fluorinated anilines and diaryl compounds within patent-protected APIs, mainly for anti-inflammatory or anti-infective agents. The compound efficiently supports regioselective substitutions and reduction steps that demand reliable handling, clear traceability, and cross-batch consistency, crucial within cGMP environments.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for APIs
    • USP/NF monograph trace requirements
    • FDA cGMP (21 CFR Parts 210 & 211)
    • EU EudraLex Volume 4 Part II

    Typical usage ratio

    • Variable from 0.1 – 0.6 molar eq. per target intermediate; batch-size adaptation based on synthetic pathway for pyridine or aniline derivatives, with excess limited to ensure complete conversion and downstream impurity control.

    Downstream process integration

    • Introduced during nitro-to-amino reduction or Suzuki coupling after solvent and temperature equilibration; maintained under nitrogen or argon to prevent side reactions through multi-stage purification and crystallization lines.

    Final product types

    • API intermediates for anti-inflammatory drugs
    • Benzoxazole and benzimidazole derivatives
    • Precursor batches for advanced generics
    • Regioselective coupling isotopologues

    3. Liquid Crystal Monomer Synthesis for Display Technology

    Key LCD panel and display component manufacturers deploy 1-Bromo-2-Fluoro-4-Nitrobenzene for synthesizing high-purity fluorinated benzene derivatives used as monomer units in nematic liquid crystal mixtures. The unique electronic and steric influence provided by its functional groups ensures sharp phase transition temperatures and dielectric properties critical in performance-driven display markets.

    Industry compliance standards

    • RoHS Directive (2011/65/EU)
    • IEC 61249-2-21 Halogen-free requirements
    • QC080000 IECQ HSPM (Hazardous Substance Process Management)
    • ISO 14001 Environmental Management

    Typical usage ratio

    • Standardized addition rates between 0.05 – 0.18 mol fraction per batch of liquid crystal monomer synthesis, adjusted for the required molecular weight and target dielectric strength for LCD functional material production.

    Downstream process integration

    • Used at the halogen substitution stage within anhydrous reactors, feeding into subsequent hydrogenation and esterification units to build target liquid crystal molecules; in-line monitored for purity and completeness before blend formulation.

    Final product types

    • High-purity nematic liquid crystal monomers
    • TN and IPS LCD panel core materials
    • Custom display mixture additives for wearable devices
    • Specialty display-grade polymer blends

    4. Dye Intermediate Preparation for Technical Textiles

    Dye substance manufacturers integrate our compound as a core intermediate in the synthesis of advanced azo and anthraquinone dye classes, prized for their colorfastness and bright chromophores required in technical fibers and performance apparel. The substrate’s electronic effects influence diazotization and coupling efficiency, aiding in the manufacture of dyes with improved resistance and specific shade profiles.

    Industry compliance standards

    • OEKO-TEX® Standard 100 dye input list
    • ZDHC MRSL (Zero Discharge of Hazardous Chemicals)
    • REACH Annex XVII for azo dye components
    • ISO 105-E01 for colorfastness testing

    Typical usage ratio

    • Typically 0.15 – 0.5 molar equivalents relative to core amines in the initial dye assembly; fine-tuned based on intended chromophore complexity and desired exhaustion rates during wet processing.

    Downstream process integration

    • Fed into nitro reduction vessels or as an activated halogen compound in diazonium coupling reactors; processed under constant agitation for homogeneous reaction and then filtered in multiple stage washing systems.

    Final product types

    • High-performance disperse dyes for polyester textiles
    • Modified anthraquinone dyes for technical fabrics
    • Sulfonated azo dye precursors for automotive upholstery
    • Reactive dye intermediates for outdoor apparel
    Free Quote

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    Certification & Compliance
    More Introduction

    Introducing 1-Bromo-2-Fluoro-4-Nitrobenzene: Practical Decisions in Modern Chemistry

    A Chemical Producer’s Perspective

    Every day in our reactors, the story of 1-Bromo-2-Fluoro-4-Nitrobenzene unfolds through careful planning, measured raw materials, and experienced hands. This compound, with the structure that places a bromo group, a fluoro group, and a nitro group on the aromatic ring, plays a role that most people outside chemical plants may never know, but for those of us on the lines, its unique fingerprint shapes a range of downstream products that reach industries well beyond our walls.

    The Build: Understanding What Goes In and Comes Out

    Putting together 1-Bromo-2-Fluoro-4-Nitrobenzene, often referenced as CAS 446-14-0, means more than shuffling reagents. Weekly, we line up raw halogenated benzenes and fine-tune their reaction environment. Adjustments to solvent batch quality and temperature don't just show up on control charts—they surface in the purity of the nitrobenzene we bottle. Producing this compound brings a sharper set of challenges than handling single-substituted benzenes or plain nitro aromatics. Bromine and fluorine rarely play nice together under reaction heat, so our Technicians must know each step, not just from textbooks but through countless production cycles. Many remember years with minor yields and more waste—practical hurdles long before today’s tightened regulations on by-products and emissions.

    What Sets 1-Bromo-2-Fluoro-4-Nitrobenzene Apart

    Small changes on a benzene ring lead to different behaviors in larger syntheses. In our experience, 1-Bromo-2-Fluoro-4-Nitrobenzene opens doors in medicinal chemistry and agrochemical research that its mono-halogenated cousins leave closed. Not every substituent combination gets you the reactivity window this molecule presents. The adjacent bromine and fluorine atoms direct subsequent substitutions with precision. In our facility, we’ve watched research partners scale up intermediates that boost selectivity in pesticide candidates. The difference doesn't just lie in the molecular fingerprint, but in the ways this compound sets up cross-coupling and nucleophilic aromatic substitutions that would stall with simpler substrates.

    Running quality control on these batches teaches discipline. Purity here isn’t a number on a label—impurities can hinder critical reactions downstream, especially Suzuki or Buchwald-Hartwig couplings running in pharmaceutical pilot plants. Over the years, customers come back asking for more stringent specs than for nitrobenzenes without halogens. The reasons range from catalyst sensitivity to regulatory filings that demand analytical traceability. We built our protocols based on these needs, refining everything from silica gel columns to final crystallizations.

    The Material Difference: Making Choices at the Bench and in the Plant

    Chemists who choose between 1-Bromo-2-Fluoro-4-Nitrobenzene and similar molecules weigh yield, selectivity, and functional group compatibility. We know this not just from sales numbers, but from phone calls and emails with process chemists fine-tuning routes to drug targets. Bromo-nitrobenzenes alone fall short where a fluoro atom can steer reactivity, and in turn, fluoro-nitrobenzenes lack the handle for certain cross-coupling steps that only bromine allows. Some ask whether this kind of intermediate could be replaced with a more basic building block. Lab feedback says otherwise; once a route’s dialed in, the risks of switching out complex intermediates grow with each failed scale-up.

    On the plant floor, we’ve seen what happens when upstream materials drift out of spec. Not all halogenated nitrobenzenes are created equal; small shifts in fluoride position or nitro placement carry through the chain, showing up in HPLC traces or in different reaction rates in the next step. Cutting corners or taking a one-size-fits-all approach rarely survives more than a few production runs. Our experience has taught us the importance of monitoring each production step to isolate not just the right molecular weight but also a clean, contamination-free batch fit for downstream transformations in regulated industries.

    Running a Tight Ship: Specifications and Real-World Challenges

    All chemical manufacturing depends on what leaves the reactor matching what was planned at the recipe stage. Specifications for this molecule aren’t dreamed up in isolation—they respond to the realities faced by researchers and industrial developers putting their trust in every delivered drum. Purity for most research applications clocks in at 98% or above, but for anything bound for clinical research or sensitive crop science synthesis, we’ve doubled down on trace-level impurity analysis. Common contaminants like regioisomers, unreacted starting material, or leftover acid scavengers present more of a challenge with the three distinct groups on this ring. Our analytics team runs batch samples through NMR, GC-MS, and HPLC, following guidance shaped by client feedback and the lessons learned from thousands of runs over years.

    Moisture control is another day-to-day concern. Trace water will interfere with many downstream steps, so drying and packaging must happen under dry air or nitrogen, with each container checked before sealing. Lessons from previous handling issues led us to overhaul packaging lines, and the result shows up in fewer customer questions and repeat orders. Quality doesn’t just happen in a lab—it requires plant workers, engineers, and supply team members agreeing on standards and constantly catching the snags we missed yesterday.

    Manufacturing for a Global Market

    Production volumes for 1-Bromo-2-Fluoro-4-Nitrobenzene shift with research cycles and crop protection trends. We keep a close ear to both contract research organizations and agrochemical clients developing the next wave of functional molecules. Some years see demand spike as new fluorinated aromatic intermediates enter patent pipelines; other seasons, pipeline delays soften orders as new priorities take center stage. Our plant runs flexible campaigns to meet contracts as well as fluctuations from R&D partners fine-tuning their development stages.

    We have learned that global compliance has teeth. Export paperwork checks for banned residues and lists every batch impurity over thresholds defined in target countries. This has reshaped how we keep documentation—not just for batch history but for actual analytical files ready for review by foreign regulators. Tightening compliance means less room for error. Every year, new guidelines shape how intermediates can be shipped, so we invest in both staff training and new equipment to head off issues. Years with stricter shipping rules forced us to redesign pallets and switch to custom-lined drums.

    Practical Applications: Beyond Abstract Chemistry

    Some buyers treat intermediates as generic tools, but the reality in active ingredient synthesis says otherwise. Medicinal chemists appreciate the push-pull of fluoro and nitro on this scaffold, which lets them assemble core fragments for kinase inhibitors and other clinical candidates. In the agriculture sector, adding both halogens can improve metabolic stability or alter environmental fate. We supply teams who have mapped out synthetic routes so tightly that even small changes in aromatic reactivity can upend weeks of research.

    Supply chain reliability makes the difference in project timelines, not just costs. Outages or late deliveries can freeze entire projects, especially for consulting labs or startups operating without large stores of material on hand. To support clients, we built up multi-week inventory buffers and maintain clearer lines of communication than we did a decade ago, logging even minor quality deviations. Chemists working with this molecule expect not just material but real technical troubleshooting—a need we’ve met by building direct support from our production chemists and not offloading all questions to sales or third-party reps.

    Environmental and Safety Considerations in Today’s Industry

    Every process involving nitrobenzenes walks a tightrope between efficiency and responsibility. We have seen major improvements in how hazardous by-products are managed. Years past saw routine venting or solvent dumping that modern systems won’t tolerate. For every kilogram of 1-Bromo-2-Fluoro-4-Nitrobenzene leaving our plant, a process of solvent recovery and neutralization runs in tandem—both for regulatory approval and to address the ongoing reality of waste handling costs. Process safety evaluations don’t just stop with the main product. Every step from bromination to nitration is reviewed, not only by internal HSE teams but often by partner audits tracing the full supply line back to us.

    Worker safety shapes everything from shift scheduling to air handling. Retrofits have added multi-stage filtration and dedicated handling rooms for raw brominated and nitrated intermediates. Reactions are run in closed systems fitted with scrubbers that we routinely test beyond required cycles. This didn’t happen overnight—it took years of reporting, analysis of previous chemical exposures, and investment in safety training. Technicians who have worked with us for years share knowledge with new hires, gradually shifting the safety culture from compliance to real-world vigilance.

    Comparing Alternatives and Making the Choice

    Companies looking to justify every chemical purchased eventually sit down to weigh this intermediate against others. Our experience supporting both pharmaceutical scaleups and fine chemicals has shown the limits of shortcuts. Switching to bromo- or fluoro-nitrobenzenes with different ring positions often delivers lower selectivity, more by-products, and longer purification times. For some, the cost benefits from switching evaporate in weeks spent troubleshooting batch failures or in unplanned revalidation of analytical methods. Route selection in chemistry, as in manufacturing, tends to reward reliability and proven track records more than chasing after short-lived cost drops.

    We work directly with end users to solve persistent issues—whether it’s troubleshooting color changes, minimizing degradation during storage, or providing impurity profiles detailed enough to meet exacting regulatory reviews. This two-way communication loop drives our product, not abstract marketing. Chemists at large and small companies share feedback we try to apply back at the source, refining both batches and the way we document everything from handling guidelines to analytical trend shifts.

    Looking Forward: Production Improvements and Ongoing Challenges

    The world demands better chemicals and greener processes every year. Our team constantly reviews existing methods and investigates alternatives aimed at reducing both turnaround time and environmental burden. Recent efforts have focused on higher-yield routes using greener solvents, automation upgrades for process monitoring, and continuous batch improvements. By keeping experienced chemists involved throughout, we find snags and risks faster than calculation alone would reveal.

    Cost pressures may never disappear, but real-world manufacturing means understanding that cheap shortcuts often show up as expenses elsewhere: in lost time, quality complaints, or regulatory backlogs. Our record with 1-Bromo-2-Fluoro-4-Nitrobenzene isn’t measured solely by tons shipped but by the repeat orders from firms who recognize the difference a consistent, high-quality intermediate makes. Some of the most rewarding moments come from calls with clients who managed a successful regulatory filing or academic team who used our batch to publish new synthetic methodology.

    Feedback and regular dialogue remain part of the backbone for how we shape both product and service. Production chemists who stand behind this material often see their work reflected in real-time troubleshooting—be it tweaking a reaction setup or helping a partner’s new technician navigate the safe handling of halogenated nitrobenzenes. In our experience, this collaboration pays dividends that can’t be matched by documents and certifications alone.

    The Bottom Line for the Future

    Delivering 1-Bromo-2-Fluoro-4-Nitrobenzene is about more than transferring a compound from vessel to drum or ticking boxes on a certificate of analysis. Our experience has shaped a focus on reliability, practical support, and open communication. Chemistry doesn't offer many shortcuts that survive the rigors of real industrial use. Experience stacks up slowly, built on small improvements and responses to real customer needs, not just abstract demands.

    We don’t take this product for granted. Every improved batch, every quality inspection passed, every customer who asks a tougher question about process control or environmental compliance forces us to refine both technique and mindset. This compound’s future—like that of our industry—rests on responsibility, technical confidence, and the willingness to listen to end users and apply lessons rapidly and transparently. We continue to back 1-Bromo-2-Fluoro-4-Nitrobenzene with the same commitment seen on our plant floors, in our labs, and through every container that leaves our doors.