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2,4-Dichloro-5-Fluorobenzoyl Chloride

    • Product Name 2,4-Dichloro-5-Fluorobenzoyl Chloride
    • Alias 2,4-DCFBzCl
    • Einecs 809-064-4
    • 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

    673033

    Product Name 2,4-Dichloro-5-Fluorobenzoyl Chloride
    Cas Number 86393-34-2
    Molecular Formula C7H2Cl2FOCl
    Molecular Weight 227.45 g/mol
    Appearance Colorless to pale yellow crystalline solid
    Melting Point 35-37°C
    Boiling Point 275°C (at 760 mmHg)
    Density 1.53 g/cm³
    Solubility Reacts with water, soluble in organic solvents like dichloromethane
    Purity Typically ≥98%
    Synonyms 2,4-Dichloro-5-fluorobenzoyl chloride
    Storage Conditions Store in cool, dry, well-ventilated area away from moisture and incompatible substances

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

    Packing & Storage
    Packing A 100-gram amber glass bottle with a tamper-evident cap and hazard labeling, securely sealed for 2,4-Dichloro-5-Fluorobenzoyl Chloride.
    Shipping 2,4-Dichloro-5-Fluorobenzoyl Chloride should be shipped in tightly sealed, corrosion-resistant containers under cool, dry, and well-ventilated conditions. As a hazardous chemical, it must be labeled appropriately and handled by trained personnel according to local regulations. Transport should comply with applicable regulations for toxic and corrosive substances.
    Storage **2,4-Dichloro-5-Fluorobenzoyl Chloride** should be stored in a cool, dry, well-ventilated area away from moisture, heat, and direct sunlight. Keep the container tightly closed and clearly labeled. Store away from bases, water, and incompatible substances. Use only with appropriate chemical-resistant materials and ensure emergency spill control and eyewash stations are nearby. Handle under an inert atmosphere if possible.
    Application of 2,4-Dichloro-5-Fluorobenzoyl Chloride

    Applications of 2,4-Dichloro-5-Fluorobenzoyl Chloride in Industrial Manufacturing

    2,4-Dichloro-5-fluorobenzoyl chloride serves as a key building block in several high-value synthesis chains within agrochemical, pharmaceutical, and specialty materials manufacturing. The following application scenarios reflect actual industrial downstream use.

    1. Synthesis of Crop Protection Active Ingredients

    Agrochemical companies primarily employ this compound for the acylation step in the manufacture of advanced herbicides and insecticides. Its reactivity and halogen profile allow for the introduction of targeted electron-withdrawing groups, contributing to bioactivity in selective weed control molecules. Manufacturers integrate this step after halogenation and before formulation, managing reaction exotherms with controlled feeding and in-situ quenching to meet purity criteria essential for regulated field use.

    Industry compliance standards

    • ISO 9001:2015 for agrochemical substance production
    • FAO/WHO specifications for pesticide technical materials
    • REACH (EC) No 1907/2006 substance registration and safety documentation
    • China ICAMA pesticide technical and formulation registration guidelines

    Typical usage ratio

    • Ranges from 0.5 to 1.35 molar equivalents relative to aminophenol or aminopyridine substrates
    • Adjusted based on targeted chlorination degree and active moiety attachment efficiency

    Downstream process integration

    • Added during the benzoylation stage of active ingredient synthesis
    • Usually introduced as a solution in chlorinated or aprotic solvents under nitrogen blanket
    • Followed by hydrolysis or catalytic hydrogenation for purification

    Final product types

    • Herbicides for cereals and broadleaf crops
    • Systemic insecticides for cotton, rice, and vegetable protection

    2. Pharmaceutical Intermediate for Fluorinated Aromatic Compounds

    This material is widely used as an advanced intermediate in the synthesis of fluorinated pharmaceutical APIs, especially in the production of certain classes of anti-inflammatory and oncological drugs. Its compatibility with Friedel–Crafts acylation and amidation steps ensures selective ring substitution. Manufacturers combine it with heteroaromatics or amines, optimizing reaction temperature and stoichiometry to meet stringent GMP impurity profiles.

    Industry compliance standards

    • Current Good Manufacturing Practice (cGMP, 21 CFR Parts 210/211)
    • ICH Q7 for Active Pharmaceutical Ingredient production
    • European Pharmacopoeia (Ph. Eur.) relevant monographs
    • Drug Master File (DMF) documentation (FDA/EDQM)

    Typical usage ratio

    • 0.8–1.2 equivalents relative to nucleophilic precursor under inert atmosphere
    • Adjusted to minimize acid chloride hydrolysis and maximize product yield

    Downstream process integration

    • Utilized in acylation or amidation step after halogenated ring assembly
    • Reacts in batch or continuous reactors, followed by purification and crystallization

    Final product types

    • Fluorinated anti-inflammatory APIs
    • Oncology drug intermediates

    3. Key Intermediate for Specialty Polymer Synthesis

    Producers of specialty polymers use this compound for aromatic monomer acylation in order to introduce fluorine and chlorine functionality into polymer backbones. This approach modifies thermal resistance, hydrophobicity, and dielectric constant in high-performance engineering plastics. Raw material charge closely follows step-growth polymerization protocols, and strict in-process controls are applied to monitor conversion rates and molecular weight distribution.

    Industry compliance standards

    • ISO 14001:2015 for environmental controls in polymer manufacturing
    • RoHS Directive (EU) 2015/863 for restricted substances in finished goods
    • UL 94 for flammability testing of plastics
    • REACH SVHC compliance for European market polymers

    Typical usage ratio

    • From 1.00 to 1.05 equivalents per diol or diamine comonomer in condensation reactions
    • Fine-tuned based on desired substitution level and chain length control

    Downstream process integration

    • Employed in step-growth or interfacial polymerization, typically as the acyl chloride input
    • Added under anhydrous conditions after initial monomer inclusion

    Final product types

    • Flame-retardant engineering thermoplastics
    • High-performance fluoro-chloro copolymers for electrical and electronic use

    4. Custom Synthesis for Advanced Liquid Crystal Materials

    Liquid crystal display (LCD) manufacturers specify this material for incorporation into core aromatic structures that define unique mesogenic properties. Its structure influences birefringence and thermal stability in final liquid crystal compounds. Synthesis typically proceeds via acylation of biphenyl or tolane units using defined anhydrous protocols, with the resulting substituted intermediates purified through fractional distillation and recrystallization.

    Industry compliance standards

    • IEC 62321 for regulation of hazardous substances in electronics
    • RoHS compliance for display devices in global markets
    • REACH restriction compliance for intermediate chemical safety
    • ISO 9001:2015 certification for specialty chemicals manufacturing

    Typical usage ratio

    • Typically 1.0 equivalent per target mesogen precursor
    • May be reduced to 0.95 equivalent to limit over-acylation side reactions

    Downstream process integration

    • Introduced during the late-stage aromatic acylation of mesogen core synthesis
    • Followed by column chromatography and solvent fractionation for purity refinement

    Final product types

    • Nematic and smectic liquid crystal mixtures for LCD panels
    • Reactive mesogen precursors for advanced display technologies
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    Certification & Compliance
    More Introduction

    Introducing 2,4-Dichloro-5-Fluorobenzoyl Chloride

    Experience from the Reactor: Real-World Value in Every Batch

    In our production halls, the character of 2,4-Dichloro-5-Fluorobenzoyl Chloride reveals itself from the earliest stage of synthesis. Our chemists and operators experience each step first-hand—handling volatile precursors, controlling temperature ramps, monitoring pressure swings. This product, with the CAS number 86393-34-2, stands apart for its unique blend of chlorine and fluorine on the aromatic ring, a structure that brings more than textbook reactivity. Familiarity with the way it behaves under various processing conditions shapes our practices on the plant floor, long before any invoice is issued or shipment leaves our gate.

    The model produced in our facility typically appears as a pale-yellow to off-white crystalline solid. We've tuned impurities down to low ppm levels as confirmed by HPLC analysis after each batch, avoiding common pitfalls like discoloration or trace hydrolysis products that could foul downstream steps. Moisture sensitivity is more than a lab warning—it means our operators store and handle raw materials and finished product under nitrogen, and we instruct our pack-out teams to seal drums quickly, so the only thing you get is the material you ordered, not a mix of acid and chloride.

    The Dichloro-Fluoro Advantage

    Chemists value 2,4-Dichloro-5-Fluorobenzoyl Chloride because the substitution pattern offers both electron-withdrawing and ortho-directing effects—a mouthful in theory, yet these traits solve practical bottlenecks. Traditional benzoyl chlorides lack this mixed halide scaffold, narrowing the range of acylations or cross-couplings that run reliably under industrial constraints. We’ve received repeated requests for special controls on isomer distribution, since a shift in halogen position changes reactivity curves and, often, the outcome of catalyst-driven steps downstream. Our in-plant QA comes from years spent resolving these issues, not just meeting a minimum threshold on spec sheets.

    Many customers use this benzoyl chloride variant in the manufacture of fluoroquinolone compounds, APIs, and agrochem intermediates. What sets it apart from both unsubstituted benzoyl chlorides and fully halogenated analogs is the balance it strikes—enough reactivity for efficient coupling, but not so aggressive that it races into unwanted side reactions. Experience has taught our operators the subtle differences in temperature ramp and mixing times needed for specific derivatives. The ortho-chlorine can make nucleophilic substitutions less prone to ring scrambling, an edge in pharmaceuticals where even minor isomer drifts trigger extra purification and regulatory headaches.

    Handling Requirements and Technical Know-How

    Past the theory, working with this material demands respect for both its benefits and challenges. Hydrolysis risk grows quickly in humid climates or when transfer lines sit idle, so our site procedures focus on tight moisture control—down to maintaining desiccant-purged hoppers during drum changeovers. Each charge is weighed, transferred, and mixed in a closed loop, the protocols honed across dozens of runs. Learning these habits came not from manuals, but from troubleshooting foaming, plugging, and off-spec color in large-scale reactors.

    In terms of batch scaling, our customers regularly share pain points about caking, clumping, and uneven melts in larger reactors. These aren’t just nuisances—they drive up handling losses and complicate filtration. Our teams learned to adjust particle size distribution through controlled cooling and milling. Years spent refining these steps results in batches that flow cleanly, pour evenly, and resist agglomeration, whether feeding an automated system or a manual charging line.

    Purity, Side-Reactions, and Analytical Reality

    Purity speaks louder than formal certificates. From our point of view, 2,4-Dichloro-5-Fluorobenzoyl Chloride owes its reliability to vigilant monitoring of trace byproducts. Side-processes, such as over-chlorination or unintended di-fluorination, are not theoretical risks—they have shown up as real, problematic peaks after a mis-set agitation speed or an accidental delay. Post-reaction acid chlorides, HPLC quantification, residual solvents—these are points of process reality, not just audit items. We di-rectly address these through double-stage purifications, temperature hold optimizations, and more.

    Customers in pharmaceuticals and specialty chemicals appreciate the batch data, but our responsibility extends to consistent inter-batch quality, not just a perfect single result. It’s not enough to “pass” a COA check; we maintain lot history and reactivity performance data that make troubleshooting downstream issues faster. The ultimate difference our process brings: less time qualifying new material, fewer adjustments on the blending floor, more predictable yields.

    Comparing to Conventional Benzoyl Chlorides

    Many users familiar with benzoyl chloride chemistries notice right away the subtle changes this dichloro-fluoro version offers. A standard benzoyl chloride will, for instance, acylate amines and alcohols rapidly, sometimes too much so—leading to over-reaction, byproduct formation, and even safety hazards in uncontrolled heats. Mono-chlorinated versions address some of this, but still invite ring substitutions and side reactions if the process window gets wide enough.

    The introduction of a second chlorine along with a para-fluorine brings real product benefit: less volatility versus trifluorinated couples, better reactivity than simple monochloro versions, and improved process control. This makes our product a favorite where high-value, high-purity downstream targets justify the investment. We’ve talked with API makers who changed their synthetic planning just to get access to the more manageable side reaction profile of this intermediate.

    In pesticide and dye applications, the same traits speed up functional group installation and cut solvent loads, making for efficiency gains neither the mono- nor trifluorinated analogs can match. Less waste, more target molecule—practical differences that show up from the tank farm to the quality lab.

    Downstream Impact: Formulators Talk

    Listening to technical leads at contract manufacturers and formulators, they often point out handling is just as crucial as yield. Lots of halogenated benzoyl derivatives turn out to be either too friable or too greasy to charge rapidly. Our decision to optimize drying and crystallization steps wasn’t just for paperwork; it came after customer complaints about filter plugging, pneumatic system fouling, and the headaches of powder “bridging” in feed hoppers. Modest improvements in our solid-state flow characteristics have allowed major processors to run longer between maintenance interruptions—a point they rarely forget.

    Our feedback loop runs both ways—reprocessing off-spec returned drums has, over the years, revealed lessons about packaging permeability, drum liner selection, and even the effects of warehouse humidity. We’ve repacked and retested hundreds of batches to ensure that the “off” aroma or visible caking doesn’t set you back a production shift. What this means in practice: less dust, more usable material, and fewer plant stoppages for everyone on the receiving end.

    Applications Beyond API Synthesis

    Plenty of users stick to classic routes in pharma, but wider application potential drives innovation. Specialty polymers and advanced coatings draw on the unique halogen patterning of this molecule for optical and surface property tuning. In agricultural chemistry, improved hydrolytic stability and resistance against photolytic degradation (from the fluorine substitution) open up new avenues compared with simple dichlorobenzoyl chlorides.

    We work directly with R&D teams to test run custom acylation reactions, especially where the balance of electron withdrawing and ring activation contributes to better selectivity or new final products. In several pilot projects, we’ve swapped fluorobenzoyl and chlorobenzoyl options, measuring improved outcome on three fronts: product yield, clean workup, and total process time. These aren’t hypothetical numbers, but the result of scaled-up reactions and real shipments—our own quality control samples included in the process development timeline.

    Advanced electronics and specialty intermediate manufacturers have pushed for finer particle sizes and specialty packaging, so we’ve installed new sieving and bagging lines in response. Tight feedback means we change as downstream requirements evolve, and we verify real-world performance—not just stability in a vacuum.

    Environmental and Safety Considerations

    Actual experience with halogenated acid chlorides means taking worker safety and environmental protection seriously. Fume extraction, emergency procedures, and spent container management form the backbone of our plant operations. Everything from loading to reactor cleaning runs through teams trained not on paper, but in annual drills and real-world situations. These protocols emerged as responses to leaks, overpressures, and unplanned exposures, shaping a culture where safety conversation flows openly between shifts and across units.

    Waste minimization for 2,4-Dichloro-5-Fluorobenzoyl Chloride comes down to discipline in both process and packaging: closed-transfer lines, quick-seal packouts, and routine audits for container integrity. Plant changes have included scrubber upgrades, smarter drum handling, and raw material tiering to control inventory aging. These add up to less process loss, fewer emissions, and more predictable supply. On the regulatory side, continuous compliance checks and partnership with local authorities keep us agile as global standards shift.

    Supply, Batch Traceability, and Continuous Improvement

    Unique challenges arise every time an order spikes on short notice or logistics run up against a storm. To keep our supply steady, we invest in buffer capacity—multiple reactors ready for surge runs, and staging warehouses with backup stocks closer to major ports. Investments in process automation didn’t come from boardroom orders, but lessons learned during missed deliveries and root-cause analysis of spec drift. Every successful rapid turnaround sharpens our edge and deepens customer trust.

    We’ve refined batch traceability to extend from raw starting acids through final shipload. Each drum carries not only a batch ID, but references to QA sign-off, process variable history, and critical operator log entries. Customers facing a synthesis hiccup get direct access to our data and, more importantly, chemists who’ve run equivalent batches under changing humidity, temperature, or feedstock purity. The aim isn’t just damage control; it’s shortening the gap between problem and solution, minimizing downstream impacts.

    Ongoing process improvement remains a running theme. The reality in chemical manufacturing is that spec drift, hardware failure, or operator turnover can lead to creeping error or background impurity over time. Routine internal challenge tests spot these shifts; root cause analysis arms us for bigger improvements. Employee feedback—whether from the packout line or the QA bench—drives dozens of small updates every year: a valve swapped, a sampling instruction tweaked, a cleaning method refocused.

    Product Integrity in Complex Supply Chains

    While business cycles and supply routes shift, the real mark of value for this product remains in how it integrates into a customer’s process. Multisite manufacturing means coordinating shipments with global regulations and documentation standards. We collaborate directly with downstream process owners to sort packaging, labeling, and customs challenges in advance, smoothing the path for both standard orders and rush re-supplies.

    The potential for cross-contamination with other halogenated derivatives gets special attention in our loading and cleaning regimes. Shared equipment carries real risk, so we maintain dedicated lines and confirmed cleanouts between batches. Periodic root-cause reviews flag the low-probability, high-impact failures that can bring down a whole campaign. It’s about focus on integrity, not just moving material.

    Our experienced teams take customer audits and regulatory site visits as a given, integrating their feedback rapidly back into batch documentation and process specifications. Every query—whether about reactivity, storage temperatures, or history of a drum—has a direct trace to the production log and QA check. This chain of custody gives customers and regulators the confidence to scale up, qualify new formulas, and manage risk far beyond the initial delivery dock.

    Challenges, Opportunities, and Looking Ahead

    The market for 2,4-Dichloro-5-Fluorobenzoyl Chloride tracks with trends in pharmaceuticals, agrochemicals, and advanced materials. Downswings in one sector nearly always mean surges in another. For us as manufacturers, this interconnectedness underscores the importance of resilience—redundancy across supply, flexibility in batch sizing, and real-world troubleshooting as conditions shift.

    Product development teams count on reliable, well-behaved intermediates to keep pace with frequent formula tweaks and process upgrades. The ability to supply material that not only “meets” but often exceeds baseline specs confers real advantage—shorter qualification cycles, more confident process scale-up, better overall plant throughput.

    Customers often challenge us with new demands: finer particle size, lower impurity limits, custom packaging, or urgent delivery windows. Each challenge exposes places where improvement matters—not just for specs, but for the experience on the user end. We’ve responded by installing in-line QC points, enhancing training for shift techs, doubling the audit cycle for sensitive raw materials, and tightening feedback loops with formulators and R&D teams.

    Complex syntheses, evolving regulatory environments, and strict process safety standards push us to continually reassess how this product fits into broader value chains. We stay close to upstream suppliers for guaranteed input quality, and downstream end users for practical feedback. Collaboration with logistics partners, regulatory agencies, and even competitors ensures information flows freely and risks are flagged early. Adapting to these dynamics with concrete plant and process upgrades keeps us nimble, no matter where the next market wave breaks.

    Summary: Quality Rooted in Experience

    We see the story of 2,4-Dichloro-5-Fluorobenzoyl Chloride not just as academic chemistry, but as the sum of every operator’s vigilance, every plant engineer’s fix, and every customer’s feedback. This perspective shapes not just what we make, but how we make it—overcoming practical, real-world hurdles so that every batch meets demanding applications in pharma, agrochem, and specialty fields. We value the work that starts on our plant floor and continues with every step, from dock reloading to downstream campaign closeout. This ongoing commitment shapes our approach, feeding a cycle where each delivery reinforces confidence, and each return brings opportunity for shared improvement and deeper partnership.