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4-Bromo-3-Fluorobenzonitrile

    • Product Name 4-Bromo-3-Fluorobenzonitrile
    • Alias 4-Bromo-3-fluoro-benzo[d]carbonitrile
    • Einecs 629-339-3
    • 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

    386490

    Productname 4-Bromo-3-Fluorobenzonitrile
    Casnumber 57381-51-8
    Molecularformula C7H3BrFN
    Molecularweight 200.01 g/mol
    Appearance White to light yellow crystalline powder
    Meltingpoint 79-83°C
    Density 1.73 g/cm³ (estimated)
    Purity Typically ≥98%
    Solubility Slightly soluble in organic solvents
    Smiles C1=CC(=C(C=C1Br)F)C#N
    Inchi InChI=1S/C7H3BrFN/c8-6-2-1-5(3-10)7(9)4-6/h1-2,4H
    Storageconditions Store at room temperature, keep container tightly closed

    As an accredited 4-Bromo-3-Fluorobenzonitrile 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 25 grams of 4-Bromo-3-Fluorobenzonitrile, sealed with a tamper-evident cap and labeled with hazard information.
    Shipping 4-Bromo-3-Fluorobenzonitrile is typically shipped in tightly sealed containers, protected from moisture and light, and labeled according to hazardous material guidelines. It must be transported as a regulated chemical substance, following local and international shipping regulations. Ensure appropriate documentation and safety data sheets accompany all shipments to guarantee safe handling and delivery.
    Storage 4-Bromo-3-Fluorobenzonitrile should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from direct sunlight and sources of ignition. Keep it separate from incompatible substances such as strong oxidizers. Ensure proper labeling and keep out of reach of unauthorized personnel. Use secondary containment to prevent environmental contamination in case of leaks or spills.
    Application of 4-Bromo-3-Fluorobenzonitrile

    Applications of 4-Bromo-3-Fluorobenzonitrile in Industrial Manufacturing

    As a direct manufacturer of 4-Bromo-3-Fluorobenzonitrile, we supply this advanced aromatic intermediate to multiple high-value chemical sectors. The following sections outline established industrial application scenarios, detailing compliance standards, precise formulation ratios, integration points in the downstream processes, and the resulting end products, based on our direct technical experience and customer feedback across global markets.

    1. Pharmaceutical Active Ingredient Synthesis

    4-Bromo-3-Fluorobenzonitrile serves as a positional building block in pharmaceutical manufacturing, particularly in the synthesis of active pharmaceutical ingredients where distinct halogenated aromatic motifs are essential for bioactivity. Multistep organic synthesis pipelines rely on this intermediate for constructing fluoro- and bromo-substituted benzonitrile moieties relevant to oncology, CNS, and anti-infective agents. Integrating this compound in early or mid-stage synthesis steps allows precise modification, which is difficult to achieve via late-stage functionalization.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for APIs
    • Ph. Eur. (European Pharmacopoeia) monograph references for intermediates
    • US FDA 21 CFR Part 211 (current GMP for finished pharmaceuticals)
    • REACH registration (EC 1907/2006) and SDS compliance for safety standards

    Typical usage ratio

    • Key intermediate usually introduced at 0.2 – 0.7 molar equivalents relative to core synthesis route; adjusted for desired active compound and total reaction scale

    Downstream process integration

    • Chemical coupling (e.g., Suzuki or Buchwald-Hartwig reactions) in initial aromatic scaffold assembly or late-stage halogen substitution

    Final product types

    • Small-molecule APIs such as novel kinase inhibitors, psychoactive agents, and anti-viral compounds

    2. Agrochemical Intermediate Manufacturing

    The material is a favored intermediate for synthesizing specialty herbicides, insecticides, and fungicides requiring precise halogenated phenyl rings to achieve target selectivity and activity. Agrochemical manufacturers exploit the dual halogen and cyano groups to build molecular frameworks for actives uniquely effective in crop protection and post-harvest treatments. Consistency in isomeric purity and traceability in reaction sequences is essential for regulatory approval.

    Industry compliance standards

    • FAO/WHO JMPR standards for pesticide ingredient assessment
    • EU Regulation (EC) No 1107/2009 for plant protection products
    • US EPA 40 CFR Part 180 (tolerances and exemptions for pesticide residues)
    • ISO 9001:2015 Quality Management Systems for agrochemical production

    Typical usage ratio

    • Typically 0.15 – 0.6 molar equivalents relative to active site formation, varied by molecular design of the intended agrochemical

    Downstream process integration

    • Nucleophilic aromatic substitution or Grignard functionalization as a halogen source and framework precursor during early-stage synthesis of patented actives

    Final product types

    • Herbicide and fungicide actives such as substituted benzamides and nitriles for soy, maize, and wheat; proprietary insecticidal candidates

    3. Electronic Chemical Intermediates for Display Materials

    In display industry supply chains, this compound is required for the production of polyaromatic intermediates for organic light-emitting diodes (OLEDs) and semiconductor films. Chemical formulators depend on the narrow reactivity profile of the bromo and fluoro groups to control polymer backbones’ electronic properties. Tight tolerance in halide incorporation improves yield and reproducibility of the catalyst docking sites essential for advanced optoelectronic materials.

    Industry compliance standards

    • IEC 62474 (Material Declaration for Products of and for the Electrotechnical Industry)
    • RoHS Directive 2011/65/EU (Restriction of Hazardous Substances)
    • ISO 14001:2015 (Environmental management in specialty chemicals)
    • JIS C 61249-2-51 (Halogen-free electronic materials)

    Typical usage ratio

    • Incorporated at 0.05 – 0.12 molar equivalents per block copolymer, optimizing chain mobility and emission characteristics; fine-tuned based on intended thermal stability and device brightness

    Downstream process integration

    • Introduced during Suzuki-Miyaura or Stille cross-coupling reactions as a functional halide unit for precise conjugated backbone construction in display chemical synthesis

    Final product types

    • OLED emitter polymers, high-purity semiconductor thin films, pre-polymers used in active display pixels arrangements

    4. Custom Fine Chemical Synthesis

    Custom synthesis companies utilize this reagent as a tailored intermediate to create specialty fine chemicals that are purposed for contract research, early-stage drug discovery, and polymer additives. The high selectivity of halogen and nitrile functional groups enables rapid modification routes essential in industries requiring structure-controlled molecular libraries. Parameterized reaction protocols ensure repeatability and traceability from lab scale to commercial batch.

    Industry compliance standards

    • ISO 9001:2015 certification for laboratory and production
    • GLP (Good Laboratory Practice, OECD Principles)
    • Environmental and occupational safety compliance under REACH (EU Regulation EC 1907/2006)
    • Custom client-specific raw material traceability and batch documentation protocols

    Typical usage ratio

    • Controlled addition at 0.1 – 1.0 molar equivalents based on synthetic pathway and downstream derivatization targets; experimental variation depends on required molecular diversity

    Downstream process integration

    • Serves as a halogen/nitrile introduction point during iterative coupling, cyclization, or functional group exchange in multistep chemical library development

    Final product types

    • Screening compounds for medicinal chemistry, tagged probe molecules, niche monomer modifiers, specialty research reagents
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    Certification & Compliance
    More Introduction

    Introducing 4-Bromo-3-Fluorobenzonitrile: Practical Insight from Chemical Manufacturing

    The work of bringing specialty chemicals like 4-Bromo-3-Fluorobenzonitrile to the world isn’t theoretical for those of us who spend our days inside the plant. This isn’t just another number on a catalog sheet—this is a product that runs through glass-lined reactors, is filtered by hands that know the difference between two points of pressure, and ends up in the drums that supply the next wave of pharmaceutical or agrochemical innovation. With over a decade dedicated to fine chemicals, 4-Bromo-3-Fluorobenzonitrile isn’t new to us, but each batch tells a different story about the things that really matter in chemical manufacturing: reliability, purity, and trust.

    Our Purpose in Making 4-Bromo-3-Fluorobenzonitrile

    Each molecule produced on our line has a destination: custom synthesis, pharmaceutical intermediates, new material science, or agricultural research. 4-Bromo-3-Fluorobenzonitrile stands up under real scrutiny because its structure opens new doors for our clients. We have seen this molecule support the synthesis of complex active ingredients in pharmaceuticals. Its nitrile group combined with the bromo and fluoro substituents gives medicinal chemists a strong starting point to develop everything from kinase inhibitors to enzyme blockers. It’s interesting how a small functional change—swapping a methyl for a fluoro or moving the bromine from the 4- to the 2-position—produces results you feel right away in downstream processes. Too many overlook these “minor” structural differences until a project stalls. We’ve learned not to.

    From Raw Materials to Pure Product: What We’ve Learned

    Manufacturing this compound is unforgiving if habit takes over. Early on, we discovered that raw material quality—particularly the selectivity of halogenated benzonitrile sources—determines much about the final outcome. Standard practice on the plant floor is to track each incoming drum and flag even the faintest hint of moisture, ensuring the cyano group keeps its reactivity and the aromatic ring stays clean without extraneous side reactions. Our QC team has caught samples where a tiny impurity changes the melting point or leaves a shadow on the HPLC trace—outcomes that cost much more in lost yield and wasted time than simply rejecting a suspect input.

    Each process step received close attention—static headspace monitors for trace water removal, and orthogonal purity verification with both NMR and mass spectrometry, beyond plain HPLC. At scale, what looks like a “pure” product from the outside sometimes reveals ghosts in the analytical run: minor halogen swaps, trace biaryl byproducts, or incomplete conversion. Our experience proves that running a pilot batch under true production conditions finds variables that lab-scale synthesis never exposes. Start-up heat profiles, stirring speed, and even the surface condition of glassware reveal themselves at plant scale. Building a process that accounts for these facts keeps lots consistent and performance predictable, both for us and for our customers.

    What Sets This Molecule Apart from the Benchmarks

    Several benzonitrile derivatives populate the market. Some use 4-bromo or 3-fluoro groups alone; others substitute the cyano group elsewhere on the ring. The dual substitution of both bromine and fluorine, with the nitrile at the para position, delivers distinctly different reactivity compared to its cousins. The bromine introduces further options for lithiation, cross-coupling (Suzuki, Stille, Heck), or nucleophilic substitution. We’ve watched medicinal chemists exploit this handle on a molecule when other routes stall out. The fluorine’s presence isn’t just for show: it influences metabolic stability and electron density, shifting physical properties, and enabling targeted fine-tuning that other benzonitriles can’t offer.

    This isn’t speculation—It comes straight from feedback we’ve received from over twenty pharmaceutical and research partners who focus on early-phase synthesis. Using the 4-bromo-3-fluoro framework often trims steps in their synthetic sequence. Instead of tacking on a halogen after introducing the nitrile, as some standard routes demand, having both functionalities on board from the outset avoids additional process risk and cost. For scale-up chemists tasked with cost-of-goods control and project managers facing tight timelines, this distinction carries weight far beyond the visible differences of position and atom count.

    Real Differences: Working with 4-Bromo-3-Fluorobenzonitrile Instead of Alternatives

    Years of hearing chemists talk about what does and doesn’t work in scale synthesis sharpens focus on “trivial” differences in intermediates. Some groups try to economize with single-substituent benzonitriles or more traditional cyano aromatics, only to get stuck on yield, side-reactions, or cumbersome purification. Testing competitive offerings and running comparative reactions, we noticed higher residual metallic impurities in some Chinese-made lots, particularly when starting from non-pharmaceutical grade raw materials. Even traces of palladium, iron, or tin from cross-coupling catalysts create downstream problems that can double workstation cleanup times or cause compliance headaches. Our own dedication to input quality and closed-system handling shows in residual test data: ICP-MS, elemental analysis, and long-term storage stability profiles document cleaner margins batch after batch.

    As a manufacturer, we control the raw material, process, and storage conditions, linking our technical documents and spectral analyses to real, physical product lots—not hypothetical data or repacked samples. Our own team signs every COA—those signatures stand behind every batch of 4-Bromo-3-Fluorobenzonitrile, with true batch traceability.

    Making the Product Fit Your Project: Not Just About the Chemistry

    Handling requests for 4-Bromo-3-Fluorobenzonitrile, we noticed early on that each customer comes with a slightly different set of purity, particle size, and documentation requirements. It doesn’t matter if you ship domestically or internationally: paperwork must match the reality inside the drums. Some projects call for 99.5% pure, tight PSD to feed automated synthesizers; others run on looser specs, prioritizing speed and cost. Our approach isn’t to offer a “premium” label for a mark-up, but to align internal QC release standards to what’s needed for safe, successful production at the next step in the chain. Overpromising purity or underplaying regulatory risks creates pain for both sides, so we focus on understanding what actually brings value in every inquiry.

    We maintain both regular and low-metal content grades, testing and clearing for elemental contaminants to meet the tightest pharma and electronics needs. Repeated solvent exchange and multi-stage recrystallization allow us to hit the narrow impurity windows critical for regulated APIs and advanced intermediates.

    Process Safety, Documentation, and Supply Chain Perspective

    No batch ships without a full paperwork audit—analytical results, chain-of-custody signatures, and packaging verification for every drum, bag, or sample vial. Timeline slip-ups lead to real bottlenecks; one shipment held because of missing transport documentation can set a client project back weeks. We understand the stakes and have put effort into integrating our documentation systems with logistics partners who speak our language, not just “tick the box” software.

    We designed our plant workflow to minimize cross-contamination. Shared equipment never runs back-to-back with incompatible products, and deep cleaning protocols keep residue from lingering batch-to-batch. The headaches we’ve faced from others' careless swap-outs or rushed turnovers motivated us to set higher internal standards, extending clean-in-place tracking and batch handover checks beyond the industry minimums. This shows in lower OOS (out-of-spec) rates, tighter release parameters, and a more predictable supply flow for every customer.

    Responding to Industry Changes and Regulatory Trends

    The past few years brought stricter regulatory eyes and faster shifts in what customers demand from their raw material partners. A growing share of buyers—from big pharma to start-ups—want detailed impurity profiles, risk assessments, and clear documentation to address not just their own QA policies but also regulatory inspections. We’ve had auditors walk through the plant, and we chose full transparency; granting access to batch logs, sampling plans, and deviation reports. This wasn't a marketing decision—it was survival and respect for the seriousness of what our materials mean downstream.

    Increasing digitization has forced changes too. We’ve invested heavily in batch tracking software that ties physical lots to unique digital identifiers. The old days of a paper trail or a spreadsheet went away once a single error caused a documentation mismatch and a rejected shipment. Now, with better digital integration, tracking every canister, analyzing return data, and documenting corrective action goes faster. Our clients don’t just get product, they get a clean chain of evidence for what’s inside.

    As new environmental and safety standards evolve, we monitor how synthetic routes and purge steps affect both operator exposure and environmental discharge. The use of greener solvents, energy-efficient heating, and closed-loop waste management isn’t marketing for us, but required investment. Down the line, our customers want proof on both regulatory compliance and progress toward sustainability targets, and we provide those details via lifecycle reporting and third-party audits.

    Product Reliability—Why We Focus on Consistency Above All

    No researcher or plant manager wants variability in starting materials. Consistency may sound like a buzzword, but in our plant daily meetings it comes down to specifics: did this lot meet internal and customer specs? Are there anomalies on the purity chromatogram? Does the halogen content drift batch-to-batch? We learned fast that a reputation hinges on not missing these details.

    Over the years, setting up real-time monitoring for temperature, pressure, and reaction progress made a massive difference. More than once, an early warning from an in-line probe or a shift on the G.C. trace saved a batch from being scrapped, and documented a learning opportunity for future runs. Our operators, trained for quick response, know how to react without waiting for managerial green-lights, shortening cycle times and eliminating avoidable errors.

    Structured operator training, rigorous adherence to work instructions, and regular audits by both QC and third-party reviewers allow us to hold our head high regarding reliability in every batch of 4-Bromo-3-Fluorobenzonitrile we send out the door.

    Working directly with R&D partners, we gather feedback on performance issues with alternative sources—stray color, solubility mismatch, or side-product formation. Based on these inputs, we tune our processes to deliver batches that customers report as cleaner to handle and easier to integrate, especially in sensitive reactions that don’t play nicely with common benzonitrile impurities.

    Building Trust Beyond the Purchase Order

    For us, trust forms the real backbone of our relationship with those who use our 4-Bromo-3-Fluorobenzonitrile. Every delivery reflects a chain of experience: people, processes, and equipment that have handled thousands of tons of halogenated aromatics safely and reliably. Our operations team stands ready to address technical or documentation requests, from extra spectral analysis to regulatory summaries and transport compliance. Fast, informed replies aren’t optional. Buyers who have dealt with unresponsive or opaque suppliers know that questions ignored today turn into disruption tomorrow. Our own business health depends on building more than a single transaction—it’s about consistent satisfaction and clear communication.

    The Bigger Picture—A Manufacturer’s Role in Progress

    Putting 4-Bromo-3-Fluorobenzonitrile into the hands of innovators bears a responsibility that goes beyond simply moving product out the gate. We play a direct part in the development of safer drugs and more sustainable crop solutions. Sourcing, producing, and shipping our benzonitrile product, we see the ripple effects through supply chains, affecting regulatory compliance, research timelines, and ultimately, patient or consumer safety. Manufacturing in this environment means that people—operators, chemists, logistics coordinators—carry as much weight in product quality as any technical spec.

    We listen to feedback from our customers and use ongoing relationships to refine process details. Not every need appears up front: sometimes a change in final use conditions, a new impurity concern, or unexpected regulatory documentation emerges long after initial order. Making ourselves available to respond quickly not only resolves problems, it leads to innovation on both sides of the table.

    There is never a perfect year or a flawless process, but building systems that acknowledge, catch, and correct mistakes keeps progress moving. Whether it comes from a thousand-kilo production run or a bottle for analytical reference, each unit of 4-Bromo-3-Fluorobenzonitrile embodies the lessons, discipline, and collaborative drive of everyone at our plant.

    Looking Forward: Meeting Tomorrow’s Demands through Manufacturing Excellence

    As new applications for halogenated benzonitriles appear, from advanced pharmaceutical scaffolds to novel agrochemical intermediates and functional materials, our experience producing 4-Bromo-3-Fluorobenzonitrile gives us perspective on how to scale responsibly. Staying ahead means not only adapting synthetic routes, handling logistics challenges, and optimizing product specifications, but also listening closely to the rapidly changing requirements of research teams, QA departments, and regulatory reviewers.

    Expectations now reach beyond chemical structure and purity. Added data traceability, cleaner supply chains, disclosure of environmental practices, and quick adaptation to customer requirements have all become must-haves, not “nice to have.” Our ongoing investments in both technology and people aim to set a benchmark in the fine chemical industry for more than just a single product, but for every way that products like 4-Bromo-3-Fluorobenzonitrile can help push scientific, regulatory, and ethical standards forward.

    Every drum that leaves our warehouse carries with it more than just a number or a COA. For us, it stands as tangible proof of what happens when knowledge, skill, and plain hard work come together to make a real impact—one molecule at a time.