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3,4-Difluoroaniline

    • Product Name 3,4-Difluoroaniline
    • Alias 3,4-Difluorobenzenamine
    • Einecs 217-614-0
    • 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

    465468

    Chemicalname 3,4-Difluoroaniline
    Casnumber 367-25-9
    Molecularformula C6H5F2N
    Molecularweight 129.11
    Appearance Colorless to pale yellow liquid
    Boilingpoint 196-198 °C
    Meltingpoint −6 °C
    Density 1.256 g/cm³
    Purity Typically ≥98%
    Refractiveindex 1.536
    Flashpoint 78 °C
    Solubilityinwater Slightly soluble
    Synonyms 3,4-Difluorophenylamine
    Smiles C1=CC(=C(C=C1N)F)F
    Inchikey GPJRVXRFDEVHMX-UHFFFAOYSA-N

    As an accredited 3,4-Difluoroaniline factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 3,4-Difluoroaniline is supplied in a 100g amber glass bottle, tightly sealed, with hazard labeling and tamper-evident cap.
    Shipping **Shipping Description for 3,4-Difluoroaniline:** Ships as a hazardous material. Package in tightly sealed, compatible containers. Store in a cool, dry, well-ventilated area. Label with appropriate hazard warnings (toxic, flammable, harmful if inhaled/ingested). Comply with local, national, and international transport regulations (e.g., UN 2810, Class 6.1 toxic substance). Handle with care.
    Storage 3,4-Difluoroaniline should be stored in a tightly closed container, in a cool, dry, well-ventilated area away from incompatible substances such as strong oxidizers and acids. Protect from light, heat, and moisture. Store at room temperature and ensure proper labeling. Use secondary containment to prevent spills, and keep the storage area equipped with appropriate spill and fire control equipment.
    Application of 3,4-Difluoroaniline

    Applications of 3,4-Difluoroaniline in Industrial Manufacturing

    As a direct manufacturer of 3,4-Difluoroaniline, we support leading global industries through advanced chemical integration. Below are verified downstream segments where our product is integral to high-value synthesis, meeting strict sector-specific standards and performance requirements.

    1. Agrochemical Intermediates (Herbicide Synthesis)

    3,4-Difluoroaniline acts as a core building block in the multi-step synthesis of key selective herbicide actives, especially within the phenoxy and pyridine classes. Leading agrochemical formulators introduce this intermediate during the condensation or amination phase, given its reactivity and substitution pattern, which enables the manufacture of actives that combat broadleaf weed species with lower application rates. Careful adherence to process impurity controls and regulatory requirements for agricultural input safety is mandatory at this stage.

    Industry compliance standards

    • ISO 9001:2015 (Quality Management Systems for chemical production)
    • REACH Regulation (EC 1907/2006)
    • FAO/WHO specifications for pesticide technical concentrates
    • Good Laboratory Practice (GLP, OECD) for impurity and residue profiling

    Typical usage ratio

    • 5–15% molar ratio in target active ingredient synthesis, adjusted for yield optimization and byproduct minimization during amination or substitution steps

    Downstream process integration

    • Added at the nucleophilic aromatic substitution or coupling stage with halosubstituted heterocycles or carboxylic acids in batch or continuous reactors

    Final product types

    • Technical grade herbicides (e.g. fluoropyrazole, diflufenican)
    • Formulated herbicide products (SC, WG, EC)
    • Pre-emergence and post-emergence weed control agents for agriculture

    2. Pharmaceutical Intermediate for Active Ingredient Synthesis

    Pharmaceutical synthesis leverages 3,4-Difluoroaniline as a selective aromatic amine source for the construction of complex bioactive molecules, particularly in the design of kinase inhibitors and fluoroarene-based drug entities. The material introduces strategic fluorine atoms that influence pharmacokinetic profiles and binding selectivity. Its use is controlled under GMP conditions, with rigorous traceability across multi-step processes in clinical API manufacturing.

    Industry compliance standards

    • ICH Q7 (Good Manufacturing Practice for Active Pharmaceutical Ingredients)
    • 21 CFR Part 211 (cGMP for Finished Pharmaceuticals, FDA)
    • Ph. Eur. or USP standards for starting material and process impurities
    • ISO 13485 for ancillary chemical use in diagnostic compound synthesis

    Typical usage ratio

    • 10–18% molar input based on target synthetic route; process chemists adjust for stage yield and impurity profile during core structure assembly

    Downstream process integration

    • Charged during heterocycle construction or Suzuki coupling steps, typically in protected multi-step synthesis of API key intermediates, under validated closed-system and solvent recovery protocols

    Final product types

    • Small-molecule APIs (e.g., kinase inhibitors, fluoroaniline-derived compounds)
    • Drug substance intermediates for further elaboration
    • Contrast agents and PET imaging precursors

    3. Specialty Dye and Pigment Precursors

    Textile and high-performance pigment manufacturers employ 3,4-Difluoroaniline in diazotization and coupling reactions to produce vibrant, chemically durable dyes used in nylon, polyester, and technical fiber coloration. The fluorine substitution imparts significant improvement in colorfastness, resistance to photobleaching, and improved compatibility with synthetic substrates. Consistent QC and compliance with harmful substance control in final dye products are essential.

    Industry compliance standards

    • OEKO-TEX® Standard 100—restricted substance requirements
    • EN 71-3 (Migration of certain elements for pigments in toys)
    • EU REACH Annex XVII for azo compounds and colorants
    • ZDHC MRSL (Zero Discharge of Hazardous Chemicals)

    Typical usage ratio

    • 1.5–3.0 mol% in diazo coupling mixtures, selected based on target hue intensity and fiber compatibility in batch or continuous dye synthesis

    Downstream process integration

    • Introduced at the diazotization or coupling stage, often with sulfonic acid components, in closed reactors with in-line monitoring of color and purity

    Final product types

    • Acid dyes for polyamide and wool substrates
    • Disperse dyes for PET fibers
    • Pigments for inks, plastics, and specialty coatings

    4. Advanced Materials for Liquid Crystal Compounds

    Leading electronics and display panel manufacturers use 3,4-Difluoroaniline in the production of liquid crystal intermediates pivotal for TFT-LCD and OLED flat panel displays. This aromatic amine provides targeted fluorination, which enhances dielectric properties and improves phase transition behavior in LC mixtures. Precision in purity and trace metal control is required to meet restrictively low defect specifications in electronics manufacturing.

    Industry compliance standards

    • IPC-6012 (Qualification and performance of printed boards)
    • IEC 61249 (Materials for printed boards and other interconnecting structures)
    • RoHS 3 Directive (EU 2015/863) for hazardous substances
    • JEITA ELS-3011B (Quality for electronic display materials)

    Typical usage ratio

    • 1–8% by weight in liquid crystal precursor mixture, dependent on the viscosity and phase rotation requirements of final LC blend

    Downstream process integration

    • Integrated during fine chemical synthesis of biphenyl or tolane-based LC intermediates, under strictly monitored microreactor or continuous-flow processes to achieve high optical clarity

    Final product types

    • TFT-LCD liquid crystal compounds
    • OLED intermediate formulations
    • Specialty liquid crystal-based photonic devices

    5. Fluorinated Polymer Modification Agents

    Producers of performance polymers and resins utilize 3,4-Difluoroaniline as a functional modifier in aromatic polyimides and related specialty resins, imparting thermal resistance, chemical inertness, and tailored dielectric properties. It enters at the stage of diamine selection for polycondensation, directly influencing the mechanical strength and thermal properties of the polymer matrix for electronics, filtration, and aerospace uses.

    Industry compliance standards

    • ASTM D5200 (Polyimide resin materials)
    • UL 94 (Flammability of plastic materials)
    • ISO 9001:2015 (Quality Management Systems in polymer manufacturing)
    • REACH registration—restricted fluorinated substance reporting

    Typical usage ratio

    • 3–10 mol% relative to total diamine input during bulk polyimide synthesis, typically optimized by material testing for each end-use application

    Downstream process integration

    • Employed in the diamine feed for batch or continuous polycondensation to form fluorinated aromatic polyimide resins; entered under inert atmosphere and high-purity solvent conditions

    Final product types

    • High-temperature polyimide films
    • Advanced circuit board laminates
    • Polymer bushings and aerospace composite components
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    Certification & Compliance
    More Introduction

    3,4-Difluoroaniline: Reliability Rooted in Chemistry

    Direct from Our Reactors to Your Applications

    In the specialty chemical field, each intermediate plays a defining role in shaping the finished quality of pharmaceuticals, agrochemicals, and advanced materials. From our vantage point on the manufacturing floor, the journey of 3,4-Difluoroaniline starts with courage to evaluate every step, batch, and detail. Our plant runs on the tight interplay between accurate raw material sourcing and rigorous process control. The goal remains constant: steady output of a product you can trust to deliver consistent results.

    Understanding the Profile of 3,4-Difluoroaniline

    The case for 3,4-Difluoroaniline (CAS No. 367-25-9) centers on the fluorination at the 3 and 4 positions of the aniline ring. The placement of these fluorines sets the molecule apart not just as another aniline derivative but as a compound uniquely suited for fine-tuned reactivity and stability in synthetic work. Our material typically arrives as an off-white to light yellow liquid, boiling just over 190°C, with a molecular weight near 129.1 g/mol. Shipping and handling revolve around maintaining this clear, reliable state, avoiding trace amine or halide contaminants that disrupt downstream synthesis.

    Why Process Experience Shapes Quality

    This product comes from years of refining bench protocols to production scale. For 3,4-Difluoroaniline, that means investing in dedicated fluorine handling systems, real-time analytics, and a hands-on operator mindset. It’s easy to overlook how much test-run data speaks to what reaches your tank. If the distillation fraction doesn’t hit the right boiling point, or the GC trace shows byproducts, you’re back to the drawing board. As manufacturers, we take direct ownership of that learning curve—adapting processes, staying on top of regulator updates, and never assuming “good enough” equals true reproducibility.

    What Sets Our Product Apart

    Direct manufacturing brings choice and control over each variable. Compared with general-purpose anilines, 3,4-Difluoroaniline’s dual fluorination puts it in a different league for nucleophilicity and selectivity. Customers using our material for API intermediates often mention reduced side reactions, more predictable purification, and easier scale-up. Competition exists from mono-fluoroaniline and isomers like 2,4- or 2,6-difluoroaniline, yet our feedback says substitution at 3 and 4 strikes the best balance between electron-withdrawing effect and manageable synthesis. Pharmaceutical chemists have told us this substitution pattern prevents certain metabolic pathways, supporting safe, active drug design.

    Batch records don’t lie: each lot is traceable, with impurity profiles and fluorine content mapped against internationally published standards. Our approach tightens the gap between batch and batch variation, based on thousands of runs logged in our facility. Environmental controls, skilled handling, and closed-loop feedback stop cross-contamination at the root. This pushes us past generic “high purity” claims seen elsewhere.

    Applications That Depend on Consistency

    Research chemists, formulators, and process engineers demand intermediates that behave predictably at any scale. Whether moving from lead optimization to pilot-plant kilo quantities or preparing tox batches, unpredictable impurities threaten to break the chain of reproducibility. Our 3,4-Difluoroaniline consistently meets high-end requirements for pharma, where downstream transformations—as in C-N couplings, acylations, or heterocycle formation—punish even slight deviation in purity or structure.

    Other teams in polymer research leverage the ortho-para fluorination for controlled backbone engineering. The difference between passing and marginal results often comes down to the subtle interplay between electron density and steric profile—factors rooted in how the starting material comes off the reactor. Agrochemical customers routinely cite field trial success, drawing a straight line back to process batches we delivered months before. Stability through transportation, resistance to light-induced breakdown, and reliable scale-up all add up to performance.

    Hands-On Quality Control and Documentation

    As a manufacturer, on-site analysis matters more than just sending vials to an external lab. We run in-house gas chromatography, liquid chromatography, and mass spectrometry for every lot. Most teams see chromatographic tracers well below the 0.5% mark for major impurities, with tighter limits imposed for non-target halogen content. Our technicians have a rule: if a batch doesn’t match the certificate numbers, it doesn’t leave the plant.

    Lot-to-lot reproducibility goes deeper than headlines on certificates of analysis. Our process chemists maintain a rolling bank of archival spectra, not just supply standard paperwork. Anyone encountering irregular solubility, melting, or reactivity downstream in their lab draws on decades of production notes and trending data before troubleshooting. We prefer transparency over marketing; if a run trends out of conventional limits, customers hear about it immediately.

    Difference from Other Difluorinated Anilines

    It’s easy to see “difluoroaniline” and lump all isomers together. The 3,4-substitution pattern behaves differently from other orientational isomers under catalytic conditions, especially in selectivity for downstream halogenation, nitration, or reduction. Several customers have shared how mismatched isomers sourced from less specialized plants led to costly project setbacks. With our specification, all isomer content falls within single-digit ppm, supported by NMR and IR checks run right at the packing line.

    Mono-fluoroanilines and 2,6-difluoro variants skew reactivity and sometimes create undesired side products that disrupt process yields in both pharmaceutical and pesticide development. Our investment in molecular fingerprinting, FTIR, and purity mapping grew out of these very lessons from customer feedback. What leaves our warehouse isn’t just “enough purity to pass”—it’s a molecule fit for its role in high-stakes chemistry, built on a record that lets customers scale up without looking over their shoulder.

    Environmental and Worker Safety in Production

    From a manufacturing standpoint, handling anilines always comes with caution flags for both environmental and workplace safety. Fluorinated derivatives present additional hurdles: tight air controls, rigorous effluent neutralization, and PPE protocols are non-negotiable. Operators wear personal gas detectors, because even trace vapor leaks can introduce risk. We maintain closed reactor vessels and downstream scrubbers that exceed local emission standards, going beyond compliance to extend the service life of our gear and protect our operators.

    The same attention drives our waste stream management. Any process fluid containing 3,4-Difluoroaniline enters a multi-stage neutralization and carbon filtration system. What leaves our gates meets the same regulatory benchmarks demanded by multinational pharmaceutical clients. We see safety not as a box to check, but as the base condition for reliable output year after year. From raw fluorinating agents to finished product packaging, hands-on protocols reduce the chance of mishaps—both for our crew and for the logistics teams moving drums off-site.

    Solutions to Production and Application Challenges

    No process runs without snags. Over the years, fouling in fluorination reactors used to trigger shutdowns, but continuous monitoring systems now flag early signs of deposit buildup, letting us intervene before a production lot turns. Downtime for equipment sanitization looks minor compared to the headache of impurity removal. On the shipping side, temperature and humidity swings once threatened product stability, so we invested in insulated, monitored containers that keep batches within a tight temperature envelope. These upgrades came directly from fielded lessons—failed shipments and customer frustration rewritten as stricter controls and smarter logistics choices.

    On the application front, we’ve sat with customer technical teams to walk through sticking points in scale-up. Sometimes labs encounter solubility issues or obscure secondary reactions when using 3,4-difluoroaniline as an intermediate. In those cases, our application chemists tap into a network of real-world troubleshooting data, ranging from solvent swaps to re-sequencing synthetic steps. Transparency with shared batch records helps identify if the root cause sits with material properties or process design.

    Traceability and Supply Assurance

    Buyers in pharmaceutical and specialty markets often voice supply chain anxiety. Traceability makes a difference—not just by batch number, but by every process step, operator ID, and instrument calibration used to make a lot. Barcode-based track-and-trace lets our team scan vials back to actual production shift records. We’ve eliminated layers of repackaging or dilution that can muddy audit trails, and this clarity often reassures customers facing FDA or EMA audits.

    Natural disasters or logistical hiccups can strain even a stable supply line. We cushion sourcing risks by maintaining on-site safety stocks, qualifying multiple raw suppliers, and doubling up on essential bearings and seals for direct production. If an earthquake or transport strike hits, downstream developers see minimal disruption. Communication flows directly between our technical account leads and customer labs, so production snags never become hidden surprises.

    What End-Users Say about 3,4-Difluoroaniline

    Input from chemists, formulation techs, and scale-up engineers shape how we produce and package each order. Teams conducting heterocyclic synthesis often mention clean reaction curves and reproducible, high-purity outputs when they switch to our version. One agrochemical client ran extended outdoor trials and credited reliable pesticide efficacy to the batch consistency of intermediates sourced directly from our reactors—not through middlemen who might introduce unknown variables or delays.

    On feedback forms and in in-person visits, customers cite actual data—not just impressions—when they talk about output stability or ease of downstream processing. Failures and learning moments hold as much value as the highlights. If a client flags an off-normal HPLC trace or notes solubility changes, our team reviews production logs, samples, and utility usage before even picking up the phone. This partnership approach grew from long-term collaboration, not sales scripts.

    Purity—and What It Really Means for Laboratories

    Smooth running operations come from purity more than most lab protocols admit. Impurity drag can sink yields on a whole project, especially in multi-step syntheses. We keep listening to customer feedback on lot performance—difficulties with crystallization, color inconsistencies, or sticky residues. By tracking these issues to production roots, equipment cleanout intervals, and specific reagent lots, we close the gap between test-tube and tank scale.

    Our purity assurance rests on proven methodology. Production QC runs include advanced GC-MS, HPLC, NMR, and titration against trace metals and halides. Expedient but careful record-keeping aligns each lot against a bank of standards. Years of production cycle reviews, not one-off certificates, push us to anticipate issues before they lead to returned drums or failed projects. End-users have a real seat at the table, guiding tweaks to filtration, post-process drying, and shipping container specs.

    Sustainability: Building Chemical Supply for the Next Decade

    From a manufacturer’s standpoint, sustainability isn’t posturing. The path from aniline to difluorinated targets generates waste streams with strict regulatory scrutiny. We route every gallon of process liquid through a multi-stage neutralization facility, scoring above local and global benchmarks for fluorinated compound control. Early investments in energy-efficient reactors and renewable-sourced utilities let us rein in the lifecycle impact of each kilogram shipped.

    Process improvements often look small—switching to lower-impact fluorinating agents, upgrading waste heat recovery, or closed-loop solvent cycles—but add up to measurable reductions in emissions and landfill volume. End-users, especially in regulated pharma and agrochem, stage in audits to review emissions and waste records before signing long-term supply deals. Sustainability targets drive procurement as much as price or purity. We see the challenge not just as cost, but as a way to secure trust for the next stage of innovation.

    Transparency and Knowledge Sharing

    Within our team, knowledge sharing carries as much weight as standard operating procedures. We keep technical documentation open between process and R&D groups. Chemists on the pilot line join regular debriefs on scale-up concerns, new impurity trends, or regulatory changes—transparency that moves faster than memos or quarterly reports. Our open-door data policy with downstream partners builds mutual understanding and smarter troubleshooting on both sides of the supply chain.

    Feedback comes in as easily as product orders do. We visit partner labs, review project progress, and swap application tips, turning customer discoveries into process tweaks or packaging changes within weeks, not cycles. Our technical meetings avoid corporate gloss—just raw data, lessons learned, and questions logged for review. Every discussion adds to the collective pool that refines purity, yields, and supply timing for everyone depending on 3,4-Difluoroaniline.

    Why The Way We Make 3,4-Difluoroaniline Matters

    As a manufacturer, we see the path to product as an ongoing collaboration—balancing safety, reproducibility, and application needs all at once. 3,4-Difluoroaniline, with its unique reactivity and selectivity, comes from equipment and experience designed for consistency across years, not just quarterly results. Lab teams who need predictable materials at scale gravitate to the places that can back up every drum with real records, not ambiguous promises. For us, delivering on this means direct accountability for chemistry at every stage—from first reactor charge to arrival at your loading dock.

    Through technical exchange and honest feedback loops, end-users shape tomorrow’s improvements as much as our own R&D. The cycle repeats: every good batch builds confidence, every flagged issue seeds a fix, every new challenge on the bench finds roots in the raw material. The result: a supply chain built not on volume, but on clear expertise, transparent process, and mutual trust in the science at the core of 3,4-Difluoroaniline.