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4-Chloro-2-Fluoroaniline

    • Product Name 4-Chloro-2-Fluoroaniline
    • Alias 4-chloro-2-fluorobenzenamine
    • Einecs 629-259-7
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
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    Specifications

    HS Code

    915442

    Chemicalname 4-Chloro-2-Fluoroaniline
    Casnumber 578-54-1
    Molecularformula C6H5ClFN
    Molecularweight 145.56 g/mol
    Appearance Light yellow solid
    Meltingpoint 55-58°C
    Boilingpoint 238°C
    Density 1.35 g/cm3
    Purity Typically >98%
    Solubility Slightly soluble in water, soluble in organic solvents
    Smiles Nc1cc(F)ccc1Cl
    Inchi InChI=1S/C6H5ClFN/c7-4-1-2-5(8)6(9)3-4/h1-3H,9H2
    Synonyms 2-Fluoro-4-chloroaniline

    As an accredited 4-Chloro-2-Fluoroaniline 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 100 grams of 4-Chloro-2-Fluoroaniline, sealed with a screw cap and labeled with hazard information.
    Shipping 4-Chloro-2-Fluoroaniline is typically shipped in tightly sealed containers, protected from light and moisture. It should be labeled as hazardous, with appropriate UN identification and hazard warnings. Transportation must comply with local, national, and international regulations for toxic and potentially harmful chemicals, ensuring secure and upright positioning to prevent leaks or spills.
    Storage 4-Chloro-2-Fluoroaniline should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from direct sunlight and incompatible substances such as strong oxidizers and acids. Avoid moisture and heat sources. Clearly label all containers and ensure chemical is kept in a designated chemical storage cabinet. Use appropriate secondary containment to prevent leaks or spills.
    Application of 4-Chloro-2-Fluoroaniline

    Applications of 4-Chloro-2-Fluoroaniline in Industrial Manufacturing

    As a direct manufacturer of 4-Chloro-2-Fluoroaniline, we supply this key aromatic amine for integration into specialized chemical synthesis across several advanced industries. Below, we present diverse, real-world downstream application areas, focusing on the specific compliance requirements, formulation ratios, process roles, and final output types within each industrial segment.

    1. Agrochemical Active Ingredient Synthesis

    4-Chloro-2-Fluoroaniline serves as a crucial building block for synthesizing selective herbicides and insecticides, particularly those requiring halogen-substituted aniline precursors for enhanced biological activity. Crop protection manufacturers use this intermediate in multi-step syntheses to develop active substances with targeted efficacy and environmental safety. Strict regulatory frameworks require product traceability and precise analytical monitoring throughout each stage of formulation and post-treatment, with attention to minimizing impurities during downstream couplings and functionalizations.

    Industry compliance standards

    • Regulation (EC) No 1107/2009 for plant protection products (European Union)
    • U.S. EPA Federal Insecticide, Fungicide, and Rodenticide Act (FIFRA)
    • ISO 9001:2015 Certified Quality Management Systems
    • Chinese GB/T 3796-2004 Safety Rules for Chemical Pesticide Production

    Typical usage ratio

    • Used at 10–25 mol% relative to final active molecule target, adjusted based on desired substitution pattern and molecular yield optimization in batch or continuous synthesis processes.

    Downstream process integration

    • Introduced as a nucleophilic aromatic substrate in the key condensation and halogen-exchange steps of technical-grade agrochemical synthesis under controlled reaction temperatures (60–120°C).

    Final product types

    • Halogenated herbicide technicals (e.g., fluorinated anilide derivatives)
    • Pre-emergent and post-emergent crop protection formulations
    • Active insecticidal ingredient concentrates
    • Pesticide intermediates for subsequent derivatization

    2. Pharmaceutical Intermediate Production

    This raw material is routinely deployed in manufacturing key pharmaceutical intermediates, particularly in the preparation of fluorinated benzene ring analogues needed for next-generation APIs in oncology and CNS therapeutic areas. Compliance with international pharmacopoeial purity specifications and batch-level traceability dominates procedural protocols, especially where downstream hydrogenation, acylation, or amide coupling reactions rely on reliable input quality and low aniline residuals. Stringent In-Process Controls (IPC) ensure residue limits and identify regulatory-relevant by-products at every handled stage.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice (GMP) for Active Pharmaceutical Ingredients
    • USP–NF and European Pharmacopoeia (Ph. Eur.) impurity guidelines
    • 21 CFR Part 210/211 (U.S. FDA cGMP regulations)
    • Chinese Pharmacopoeia standards for intermediate purity

    Typical usage ratio

    • Commonly specified at 5–15 mol% versus targeted pharmaceutical core during synthesis, with adjustments for desired molecular modifications and conversion efficiency.

    Downstream process integration

    • Fed as a primary intermediate into halogenation, acylation, or Suzuki cross-coupling reactions under controlled conditions (purity >99%, water content <0.5%) and batch-wise validated.

    Final product types

    • Fluorinated drug intermediates
    • API precursors for anticancer compounds
    • CNS-targeted small molecule drug scaffolds
    • Fine chemicals for further pharmaceutical transformations

    3. Dye and Pigment Intermediate Manufacturing

    Our product frequently enters the synthesis of specialty dyes and pigments for use in textile, plastics, and specialty coatings production, especially where unique halogen substitution patterns improve lightfastness and chromatic durability. Producers adhere to strict safety and environmental standards, preventing aromatic amine contamination in end-use applications and optimizing reactivity for electrophilic substitution and diazotization procedures. Continuous monitoring of both reaction yields and hazardous by-products remains essential for compliance and customer acceptance testing.

    Industry compliance standards

    • Registration, Evaluation, Authorisation and Restriction of Chemicals (REACH, EU)
    • OEKO-TEX Standard 100 Annex 6
    • ZDHC Manufacturing Restricted Substances List (MRSL)
    • ISO 9001:2015 Quality Management for chemical intermediates

    Typical usage ratio

    • Employ 8–20 wt% based on target pigment molecule, with precision alterations to produce specific absorption or reflection characteristics in the final dye product.

    Downstream process integration

    • Supplied to diazotization and subsequent coupling units for production of azo or heterocyclic pigment frames, managed in both batch and semi-continuous reactors.

    Final product types

    • High-performance aromatic azo dyes
    • Halogenated pigment intermediates for automotive coatings
    • Textile reactive dye ingredients
    • Colorants for plastic compounding and masterbatch production

    4. Specialty Polymer Synthesis

    Chemical manufacturers incorporate this halogenated aniline into advanced polymeric material formulations, particularly for engineering plastics and specialty resins where additional halogen content boosts flame retardance and weather resistance properties. End users implement detailed quality checks for monomer purity, impurity carryover, and impact on final polymer chain architecture. Compliance focuses on robust process safety and VOC emissions limits throughout the closed-system aminopolymerization and prepolymer preparation stages.

    Industry compliance standards

    • ISO 14001:2015 Environmental Management for manufacturing
    • EN 14582:2016 for determination of halogens in polymers
    • REACH Regulation for new monomer substances (EU)
    • RoHS Directive (Restriction of Hazardous Substances) for electronics polymers

    Typical usage ratio

    • Introduced at 3–10 mol% relative to co-monomers, adjusted according to final polymer backbone requirements and targeted functional properties.

    Downstream process integration

    • Reacted in initial aminopolymerization, imidization, or condensation steps under controlled anhydrous conditions, ensuring consistent incorporation and homogenous dispersion.

    Final product types

    • Engineering thermoplastic base resins
    • Flame-retardant polymer additives
    • Fiber-reinforced composite matrix prepolymers
    • High-durability coatings for automotive and electronics

    5. Fine Chemical Research and Synthesis

    CROs, academic groups, and fine chemical producers rely on this raw material for custom molecule construction in R&D settings, such as for SAR (structure-activity relationship) studies and pilot-scale feasibility runs on advanced chemical entities. Here, maximum data integrity and traceable documentation accompany each transaction, and usage ratios shift per targeted synthetic route and downstream derivatization complexity. Research laboratories monitor process safety closely and quantify input impacts on yield, selectivity, and product stability.

    Industry compliance standards

    • OECD Principles of Good Laboratory Practice (GLP)
    • ISO/IEC 17025 Testing and Calibration Laboratories
    • REACH Annex XVII Research Exemption for small-scale synthesis (EU)
    • China National Standard GB/T 22241-2008 for research chemicals

    Typical usage ratio

    • Applied over a range of 1–50 mmol scales, with ratio dependent upon target molecular design and reaction screening schedule.

    Downstream process integration

    • Used in gram-to-multigram runs via nucleophilic substitution, cross-coupling, and benzylic modification routes for creation of novel compounds or advanced screening sets.

    Final product types

    • Tailored fluorinated analogues for biological testing
    • New heterocyclic scaffolds
    • Reference standards for regulatory filings
    • Pilot-phase intermediate libraries
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    Certification & Compliance
    More Introduction

    Introducing 4-Chloro-2-Fluoroaniline from a Manufacturer’s Perspective

    Understanding 4-Chloro-2-Fluoroaniline

    Working with fine chemicals every day, we put a premium on details in production and quality, especially with specialty items like 4-Chloro-2-Fluoroaniline. Over the years, this compound has become a familiar sight in our facility: a solid white powder, easy to handle and store compared to less stable analogs. Our associates have seen it journey from the earliest batch reactors to finished goods ready for specialist industries. The structure—an aniline backbone decorated with a fluorine at the ortho position and chlorine at the para—has practical implications far beyond the lab bench. We’ve watched it find its own niche in a vast range of chemical processes, each one demanding the consistency and purity our crews learn to provide through hands-on know-how.

    This compound, known among chemists as 4-chloro-2-fluoroaniline, bridges the gap between basic aromatic amines and engineered intermediates built for custom syntheses. Unlike more basic anilines, the presence of chlorine and fluorine brings distinctive reactivity. Chemists on our development teams often say this pairing is hard to replicate. They’ve tried routes swapping chlorine for bromine, but the behavior shifts—boiling points, reaction times, and downstream reactivity all show noticeable variations.

    Specifying the Product: Beyond the Datasheet

    When designing a continuous process, an engineer needs to know how a material will behave from bulk storage to workup and filtration. Our experience preparing 4-Chloro-2-Fluoroaniline in industrial lots sheds light on more than just melting points and assay percentages. Tracking each batch—from solvent choice to final drying—our production team records appearance, odor, solubility, and stability profiles. In our process, purified material typically presents as a solid mass, easy to flake or grind without caking, but quick to dissolve in polar aprotic solvents. These qualities reduce downtime in scale-up syntheses.

    We use routine spectroscopic verification: NMR, GC, and HPLC records back up every kilogram. Internally, we’ve learned not to skimp on in-process checkouts. Even subtle impurities change the game during coupling steps or halogen exchange reactions. On days where a tank feeds too quickly or a dryer runs hot, operators catch these shifts and keep output within tight specifications. We take pride in upholding purity standards that meet more than just regulatory minimums; they match the demands of our most exacting partners in pharma and agrochemicals.

    Main Uses Driven by Chemical Characteristics

    From our loading docks to shipping samples for field testing, 4-Chloro-2-Fluoroaniline has proven itself in several sectors. Custom synthesis shops rely on it to build up heterocyclic compounds. Their feedback tells us two things: the electron-withdrawing nature of the fluoro and chloro substituents tunes the aniline ring for specialized transformations, and the product’s reactivity suits downstream nucleophilic aromatic substitution steps.

    In pharmaceuticals, process chemists prize it for assembling kinase inhibitors and other modern drug candidates. The presence of a fluorine atom at the ortho position shields parts of the molecule from undesired substitutions while the chlorine allows selective coupling with boronic acids, azides, or alkoxy groups. By sourcing highly pure 4-Chloro-2-Fluoroaniline, drug manufacturers shave days off route scouting. Over multiple projects, our partners have reported faster setup, cleaner product isolations, and fewer byproducts.

    Agrochemical teams value a similar reactivity but apply it differently—targeting herbicides and insecticides that demand robust, consistent intermediates. Our teams have worked hand-in-glove with collaborators to optimize derivatization reactions. And where mass-market anilines struggle to deliver thermal or storage stability, this fluorinated-chlorinated compound holds up under demanding plant conditions.

    Real-World Experience and Challenges in Manufacturing

    Our company’s bench-scale chemists and plant operators have become deeply familiar with the nuances of making and handling 4-Chloro-2-Fluoroaniline. Production often starts with fluorinated nitrobenzene and proceeds through reduction and halogenation. Every stage introduces risks: over-reduction, incomplete halogen exchange, or contamination with ortho-chloro or para-fluoro analogs. Some years ago, several lots showed stubborn color changes due to trace overhalogenation. Plant staff took initiative, adjusting timing and filter media. Gradually, purity profiles snapped back into line.

    One persistent challenge is moisture control. This product, though more forgiving than some amines, still absorbs water during humid shifts, forming tiny clumps in large storage bins. Only careful rotor design for drying—plus dehumidified storage—delivers the free-flowing texture customers count on. Feedback from industrial partners led us to overhaul our bin liners and warehouse climate control. Logistics rarely gets the spotlight, but in the daily reality of scale production, warehouse staff makes all the difference.

    Transport is another headache when regulations tighten. Years ago our logistic teams spent weeks updating SDS documentation as minor regulatory lists added or shifted. Regulatory shifts now come faster. We relearn compliance each year, updating training and rolling out fresh documentation for each regional export. Consignment tracking helps keep customers informed and our crews sharp.

    Product Differences: Better, Not Just Different

    In the crowded market of substituted anilines, any new product must justify its presence. To our staff, 4-Chloro-2-Fluoroaniline stands apart for tangible reasons. Regular aniline has a wide sphere of use but lacks the built-in selectivity modern synthesis prizes. Add only a chlorine or only a fluorine, and you get predictable changes in reactivity, but not the balance needed for complex coupling. Our compound, with both, walks the line between electron withdrawal and manageable reactivity. It succeeds where 2-fluoroaniline falls short in subsequent halogenation or where 4-chloroaniline lags in elemental substitution. Reactions proceed cleaner, with less need for purification by labor-intensive crystallization or chromatography.

    With real-world batches, you see these differences as soon as you run an amide formation or aromatic substitution. Partners in pharmaceutical scale-up tell us that single-impurity profiles lead to greater yields over mixed-substituent blends. Our own pilot plants comparing related compounds found that using our product reduced waste solvent usage and halved reaction time during amidation. Details from batch records support those claims—less rework, fewer emergency stops, and steadier output even in long runs.

    On the supply side, 4-Chloro-2-Fluoroaniline manages to avoid several trade-offs. Brominated analogues sometimes bring smoother reactivity but at much higher cost and regulatory scrutiny. The combination of chlorine and fluorine keeps both input costs and compliance in a tolerable zone. We’ve tailored feedstock sourcing, working with trusted regional partners and refining our own purification so that the finished chemical remains accessible to both small development labs and bulk producers.

    Supporting Consistent, Responsible Use

    Behind every kilogram leaving our facility is a record of hands-on problem-solving. We know our customers need more than a guaranteed spec list. Our engineers field direct calls from users who run into problems: solubility concerns, storage hiccups, or route changes that suddenly demand higher purity or alternate particle sizing. Over recent years, requests for ultra-low metal content have grown. In response, we retuned reactor selection and adopted more frequent filter changes. Quality teams tested successive lots until metal readings dropped below demanding thresholds.

    In the field, users across pharmaceuticals and crop science face increased scrutiny not only on raw material purity but traceability, workplace safety, and process residues. Our operator training covers updated guidance from new ICH and environmental regulations, which trickle down into routine batch logs and sample tracking. The whole plant works together to respond fast when regulators revisit permissible exposure limits or flag new impurities for scrutiny.

    A product like 4-Chloro-2-Fluoroaniline stands at the intersection of modern chemistry’s big pressures: deliver quickly, avoid contaminants, and back it all up with data. Having full in-house manufacturing means everyone at the site can see quality issues firsthand; technicians swap feedback with lab staff, and log control systems prompt on-the-spot calibration checks instead of waiting for data to drift.

    Building on What Works: Long-Term Partnerships and Continuous Improvement

    Relationships drive improvements. Some customers stay with the same supplier year in, year out; that trust only comes from consistently meeting the tiny demands no datasheet captures. Over time, we’ve pivoted not just the chemistry but the way the plant supports customers. Years ago, we introduced a change management system so that project managers and QC could trace every raw material lot and every tweak made to the process. The learning curve was real, but tighter feedback loops now let us spot deviations quicker, saving lost time from delayed or failed scale-ups at the customer end.

    They’ve taught us just as much. Several clients working in continuous flow chemistry pointed out that unanticipated, trace-level impurities built up in their reactors with traditional grades. Opening up our process to review with them, we found one obscure elution from a side reaction. It took weeks of team effort and pilot testing to reformulate and dial back the problem, but now both sides benefit—better yield, easier downstream workup, and fewer unplanned stoppages.

    In today’s chemical industry, adaptability wins. As new applications for 4-Chloro-2-Fluoroaniline emerge—specialty coatings, advanced polymers, or niche catalysts—they often come with unfamiliar scaling or purifying challenges. Lean manufacturing teaches us to adapt. On the floor, operators and engineers share real-time findings at daily standups. Researchers roll out pilot lots to early adopters, taking in direct feedback. Often, even small changes in particle size control or crystal habit can make the difference between headaches and headache-free processing.

    Pride in Manufacturing: Ground-Level Stories

    Many in our crew started mixing drums or running stills years back. They remember handling trickier, less predictable products before automated controls arrived. Everyone in the shop takes pride seeing the evolution: tighter specs, less waste, and a product line that helps some of the world’s leading companies move forward. When a customer’s line stops due to a gum-up from low-grade batches, they call us. We have seen plenty of scrap bins fill and process tanks slow from mixed or off-color lots. Every team member—from maintenance to ops specialist—knows the cost and works to head off those issues long before they reach shipping.

    It’s the details only daily grinders know: how a crystalline powder pours from the drum, how to spot early signs of polymerization, and how to recognize a drum out of spec by odor before paperwork catches up. On the best days, a clean run makes for simple dispatch. But more often than not, success means jumping in, troubleshooting, and learning. Documentation matters, but it’s only as good as the people who use it, track trends, and bring lessons back every shift.

    Looking Ahead: Sustainability and Industry Trends

    Pressure grows each year to reduce environmental impact and boost transparency. We source starting materials as locally as possible and work with partners who share our approach to waste minimization and cleaner effluents. In our own plant, solvent recovery and process water recycling have reduced total output waste by a full quarter over the last five years. Modern 4-Chloro-2-Fluoroaniline manufacturing integrates these practices not because they look good on paper, but because regulatory and community demands force everyone in the chain to do better.

    Customers now audit not just quality but sustainability. They want up-to-date reports, down to energy consumption per kilogram, and packaging with clear end-of-life routes. Improvements come hard-fought: fine-tuning driers, balancing line speed with emissions, or trimming unnecessary packaging. We keep at it because we see the difference in long-term contracts, audits that run smoothly, and neighbor communities that support our ongoing operations.

    From the earliest lab batches to shipping tankers bound for three continents, our work with 4-Chloro-2-Fluoroaniline reflects lessons earned from the ground up. We listen, adapt, and stay hands-on in every aspect of production. For our crews, there’s satisfaction in seeing chemistry deliver—batch after batch, drum after drum, with quality and reliability that make a real difference on the customer’s end.