Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing admin@sinochem-nanjing.com 3389378665@qq.com
Follow us:

2,4-Difluoroacetanilide

    • Product Name 2,4-Difluoroacetanilide
    • Alias N-(2,4-Difluorophenyl)acetamide
    • Einecs 252-719-8
    • 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

    945949

    Chemical Name 2,4-Difluoroacetanilide
    Molecular Formula C8H7F2NO
    Molecular Weight 171.15 g/mol
    Cas Number 367-29-5
    Appearance White to off-white solid
    Melting Point 61-65°C
    Boiling Point 312-313°C
    Density 1.32 g/cm³
    Solubility In Water Slightly soluble
    Synonyms N-(2,4-Difluorophenyl)acetamide
    Structure Formula C6H3F2(NHCOCH3)-2,4
    Smiles CC(=O)NC1=C(C=C(C=C1)F)F
    Storage Conditions Store in a cool, dry place
    Purity Typically ≥98%

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

    Packing & Storage
    Packing 250g of 2,4-Difluoroacetanilide supplied in a sealed amber glass bottle with a screw cap, labeled with hazard and product information.
    Shipping 2,4-Difluoroacetanilide is shipped in tightly sealed containers to prevent moisture absorption and contamination. It should be handled with care, avoiding direct contact and inhalation. The package is labeled according to regulatory guidelines and transported under ambient conditions, unless specific storage temperatures are required. Ensure compliance with all relevant chemical shipping regulations.
    Storage 2,4-Difluoroacetanilide should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from incompatible substances such as strong oxidizers. Protect from light and moisture. Store at room temperature and keep away from sources of ignition. Ensure proper labeling and segregate from food and drink. Handle using appropriate personal protective equipment (PPE).
    Application of 2,4-Difluoroacetanilide

    Applications of 2,4-Difluoroacetanilide in Industrial Manufacturing

    2,4-Difluoroacetanilide functions as an essential intermediate in several specialty chemical manufacturing sectors. Our production facility supports high-volume contract customers across regulated domains, ensuring precise formulation integration and continuous batch traceability. The downstream uses below reflect actual manufacturing deployments, governed by strict compliance protocols and customer requirements.

    1. Agrochemical Synthesis (Herbicide Intermediate)

    Major agrochemical producers use 2,4-difluoroacetanilide for targeted grass and broadleaf herbicide formulations. The compound enters early-stage synthesis, providing a key difluoroaromatic structure for high-selectivity active ingredients. Formulators adjust charge ratios to optimize activity spectrum and environmental persistence, ensuring regulatory compliance throughout multi-step synthesis. Downstream blending practices require purity and controlled impurity profiles. Continuous process verifications track each batch through final product release for agricultural use.

    Industry compliance standards

    • FAO/WHO Specification 357/Agrochemicals (technical & impurity limits)
    • REACH Annex II for agrochemical intermediates
    • ISO 9001:2015 for process management in agro-inputs
    • US EPA 40 CFR Part 174 for inert ingredients in pesticides

    Typical usage ratio

    • Reactant loading at 0.2–0.8 mole per mole of final active ingredient
    • Charge ratio adjusted by stoichiometry and impurity control needs
    • Formulation batch sizes range 200–2,000 kg
    • Process purge and recycle rates determined by downstream validation

    Downstream process integration

    • Introduced via batch reactor preblending with solvent phase
    • Undergoes acylation, halogen exchange or ring coupling as core steps
    • In-line QC for identity and purity prior to final formulation
    • Wastes handled under regulated chemical destruction protocols

    Final product types

    • Selective post-emergence herbicide technical concentrate
    • Co-formulated crop protection active ingredients
    • Granular and microencapsulated herbicide products
    • Pre-mix blend additives for contract pesticide formulators

    2. Pharmaceutical Intermediate for Active Compound Synthesis

    API manufacturers incorporate this intermediate when constructing difluoroaromatic fragments essential for select antimicrobial and antineoplastic agents. The compound participates in controlled, cGMP-validated synthesis schemes, forming part of active compound cores via amide coupling and electrophilic substitution reactions. Highly controlled environments, validated cleaning, and trace documentation are required, backed by full analytical release testing specific to pharmaceutical APIs. Method optimization is based on route feasibility, yield, and impurity minimization.

    Industry compliance standards

    • ICH Q7: Good Manufacturing Practice for APIs
    • 21 CFR 211 and 21 CFR 210 for drug substance production
    • European Pharmacopoeia (Ph. Eur.) monographs on intermediates
    • USP General Chapters for process validation

    Typical usage ratio

    • Introduced at 0.3–1.1 mole per mole of target API step
    • Adjusted per route efficiency and desired yield
    • Pilot lots 10–100 kg, scaled to multi-ton cGMP batches
    • Charging guided by analytical in-process control

    Downstream process integration

    • Charged after initial condensation or amidation step
    • Flow-reactor or batch process, depending on plant setup
    • Strict deviation and cleaning logbook for intermediate handling
    • Product released based on chromatographic impurity profile

    Final product types

    • Registered pharmaceutical drug substances (API)
    • Bulk intermediates for antimicrobial agents
    • Oncology chemical entities for oral or injectable forms
    • Exported GMP intermediates for generic drug production

    3. Fine Chemical Production for Specialty Dyes and Pigments

    Manufacturers in the dye and pigment sector employ this difluoroaromatic compound to construct high-performance specialty colorants. As a building block, it imparts increased solubility and stability in final pigment structures, supporting application in plastics, fibers, and high-grade coatings. Manufacturing lines follow strict batch color consistency and spectral control. Analytical method development supports custom pigment property validation for downstream customers.

    Industry compliance standards

    • DIN EN ISO 9001:2015 for specialty chemicals
    • GHS/CLP compliance for colorant safety labeling
    • EN 71-3 for pigments used in toys
    • ISO 787/5 Pigment Testing Procedures

    Typical usage ratio

    • 0.5–2.0 mole per mole in pigment condensation syntheses
    • Reactant ratio based on target chromophore structure
    • Large batch production: 500–5,000 kg
    • Testing at laboratory pilot before full-scale up

    Downstream process integration

    • Introduced in the primary colorant condensation reactor
    • Controls fluorine content for pigment lightfastness
    • Integration with solvent and acidic catalyst dosing
    • Crude pigment precipitated, washed, and filtered under controlled pH

    Final product types

    • High-performance organic pigment powders for plastics
    • Reactive dye intermediates for textile coloration
    • Specialty pigments for automotive coatings
    • Industrial masterbatch colorants

    4. Polymer Additive Precursor in Engineering Plastics

    Producers of high-specification engineering plastics use 2,4-difluoroacetanilide as a monomeric precursor for specialty aromatic polymers. Its presence in the feedstock imparts chemical resistance, reduced flammability, and tailored thermal properties. Downstream blending and polymerization depend on tight color and molecular weight control. Continuous gravimetric feed and in-line monitoring allow for batch-to-batch consistency over high-throughput production runs. Custom specification development aligns with end-use certification requirements.

    Industry compliance standards

    • ISO 9001:2015 for high-performance polymers
    • UL 94 for flammability of plastics materials
    • REACH Article 56 Registration for polymer precursors
    • RoHS Directive 2011/65/EU (where applicable)

    Typical usage ratio

    • Integrated at 0.1–0.7 mole per mole main monomer, depending on property target
    • Adjusted by melt flow and polymerization grade
    • Production batches from 100 kg up to 20 metric tons
    • Ratio set for flame retardancy and chemical compatibility

    Downstream process integration

    • Fed into bulk polymerization after monomer pre-drying
    • Dosed through automated gravimetric systems
    • Chain termination or extension step determines degree of incorporation
    • Resin finishers use in-line GC/FTIR analysis for verification

    Final product types

    • Specialty aromatic polyamide and polyimide resins
    • Flame-retardant plastic automotive components
    • High-resistance electrical housings
    • Custom thermoplastic masterbatches

    5. Chemical Intermediate in Electronic Materials Manufacturing

    Producers of advanced electronic materials utilize this intermediate to introduce fluorinated segments into photoresist and encapsulant resins. The presence of difluoro moieties boosts dielectric strength and enhances moisture resistance in microelectronic assembly. Precise feeding ensures lot-to-lot uniformity demanded by downstream semiconductor and printed circuitry clients. All production is monitored under ISO and green chemistry frameworks, supporting both performance and regulatory demands for high-technology materials.

    Industry compliance standards

    • IEC 61249-2-21 for base materials of printed boards
    • ISO 14001:2015 for environmental management
    • JPCA-ES01 for electronic substrate materials
    • REACH Regulation (EC) No 1907/2006

    Typical usage ratio

    • 0.05–0.3 mole per mole in resin precursor batch
    • Ratio fine-tuned for dielectric and adhesion properties
    • API-scale synthesis: 20–200 kg per run
    • Adjusted based on thickness, resistivity, and processing window

    Downstream process integration

    • Dosed into pre-polymer reactor with solvent and initiator
    • Undergoes co-polymerization with bisphenolic or epoxide monomers
    • Process monitored with DP meter for molecular weight
    • Resins extruded or cast into films and encapsulant sheets

    Final product types

    • Photoresist resins for semiconductor wafer fabrication
    • Dielectric coatings for flexible printed circuit boards
    • Electronic encapsulating materials
    • High-barrier adhesives for microelectronics
    Free Quote

    Competitive 2,4-Difluoroacetanilide prices that fit your budget—flexible terms and customized quotes for every order.

    For samples, pricing, or more information, please call us at +8615371019725 or mail to admin@sinochem-nanjing.com.

    We will respond to you as soon as possible.

    Tel: +8615371019725

    Email: admin@sinochem-nanjing.com

    Get Free Quote of Sinochem Nanjing Corporation

    Flexible payment, competitive price, premium service - Inquire now!

    Certification & Compliance
    More Introduction

    2,4-Difluoroacetanilide: Experience in Manufacturing Specialized Fluoroaromatic Intermediates

    Our Commitment to Quality in the Field of Fluorinated Chemicals

    Over years working with fine and specialty chemicals, the path to producing 2,4-difluoroacetanilide has been shaped by practical demands from pharmaceutical and agrochemical development. This molecule, defined by its difluorinated aromatic structure and stable acetamide group, caught our attention early because of its usefulness as a core intermediate. Fluorination on the aromatic ring often brings a distinct performance advantage in downstream synthesis—especially when compared to traditional acetanilides without halogen substitution.

    In our experience, subtle variations in substitution produce significant changes in reactivity and handling. 2,4-difluoroacetanilide stands out due to its paired fluorine atoms at the ortho and para positions. This configuration offers both electronic effects and a degree of steric influence not present in its mono-fluorinated or non-fluorinated counterparts. As a result, this molecule frequently appears as a preferred building block in discovery chemistry teams working toward fluorinated analogues, whether for bioactivity tuning or material science innovation.

    Manufacturing and Handling: Lessons Learned from Scale-Up

    We do not approach the synthesis of 2,4-difluoroacetanilide as a routine batch operation. Each run begins with clear starting materials and careful control of temperature, atmosphere, and reaction timing. During scale-up, any deviation—even slight—can shift the selectivity or produce unwanted over-fluorination. Our facilities invest in precise dosing and containment solutions, eliminating cross-contamination and unwanted exposure to raw fluorinating agents. Our teams stay focused both on target yield and downstream purification, streamlining crystallization and drying to reduce unwanted side products and residual fluorides.

    Each drum or container leaving our facility reflects repeated in-house analytical checks and practical packaging decisions. We learned early that fluorinated intermediates, particularly those like 2,4-difluoroacetanilide, attract moisture and degrade if sealed incorrectly. For that reason, we opt for lined containers and minimize free headspace—practices shaped not from theoretical advice but from hands-on experience rerunning operations due to premature degradation. These lessons direct our logistics and storage, so our product reaches chemists in a workable, consistent condition.

    Comparison with Analogues: Why Placement of Fluorine Matters

    Many teams ask for side-by-side performance with similar compounds, such as 2-fluoroacetanilide or 4-fluoroacetanilide. Our records make it clear that the dual fluorine effect, specifically at 2 and 4 positions, changes both physical and chemical behaviors in meaningful ways. Beyond melting point and solubility, the alteration of electron density on the ring can speed up or slow down nucleophilic aromatic substitution or affect overall selectivity in further transformations. In synthesis routes where regioselectivity or activation is essential, our customers observe better yields and purer downstream products with 2,4-difluoroacetanilide than with mono-fluorinated analogues.

    Part of this difference comes from the way two fluorine atoms modulate the acetanilide's properties. The 2,4-disubstitution reduces unwanted side reactions and gives the acetamide unit the right balance of reactivity and stability. As a manufacturer, we've run a variety of conversions with this intermediate—testing reductive, oxidative, and substitution pathways. Time after time, we find reduced byproduct formation and easier isolation, which translates into fewer repurification steps.

    Practical Applications Draw on Stability and Selectivity

    Chemists seeking reliability in lead optimization value predictability and performance. 2,4-difluoroacetanilide has demonstrated its worth in several patent-protected routes to active pharmaceutical ingredients and agricultural agents. The stability of the acetanilide in storage and handling allows teams to operate with fewer concerns about decomposition or loss of fluorine—common issues in less robust halogenated intermediates. During our collaborations, researchers often highlight how the molecule facilitates downstream reactions, such as amide hydrolysis, acyl transfer, or halogen exchange, without introducing unwanted impurities or degradation products.

    Creating kilogram- to ton-scale batches for process development projects challenges our reactors, logistics, and analytical protocols. Each scale brings new complications—heat transfer, mixing, and product isolation all shift as vessels grow. Through every scale-up campaign, we track impurity profiles and optimize our workup protocols to safeguard purity. Over time, we’ve built a reliable supply that supports both laboratory trials and market launch quantities, extending from grams to multi-ton shipments.

    User-Focused Experience: Partnering on Your Projects

    Feedback from our partners shapes every process cycle. A formulator working in crop protection wants batch consistency and reliable delivery. For pharmaceutical clients, small batch samples support rapid screening, while large volumes back pilot production and regulatory submissions. Direct discussions with our technical service team give insight into what’s working and what can be improved, whether by tightening specifications, modifying packaging, or expediting logistics.

    We understand the demands posed by modern supply chains. Time and again, global uncertainty and shifting regulations test resilience, so we maintain reserve stocks and redundant sourcing of precursors to guarantee continuity. Traceability, batch records, and an open line to our plant engineers ensure clients see exactly what goes into each container and how it meets their requirements.

    Supporting Downstream Innovation: More Than a Raw Material

    Too often, fine chemicals are treated with a one-size-fits-all mentality, leading to surprises later in the development process. Our work with 2,4-difluoroacetanilide goes beyond mere supply—we partner with chemists to ensure they understand reactivity, safe handling, and how our material will behave in their unique process environment. Detailed spectral characterization accompanies every batch, matched against tight in-house specifications for purity, moisture, and residual halide content.

    For those developing new routes or novel scaffolds, our technical team draws from hands-on experience in synthetic methodologies. We’ve optimized conditions for common reactions—such as Sandmeyer-type halogenation, selective amide cleavage, and multi-step coupling. Our customers draw advantages by working directly with the manufacturing source, allowing for custom specification discussions and fast feedback on process adjustments. These capabilities would not be possible without continuous investment in pilot and commercial production infrastructure dedicated to aromatic fluorination.

    What Sets 2,4-Difluoroacetanilide Apart in Real-World Applications?

    Our comparison studies highlight clear distinctions. Mono-fluorinated acetanilides offer incremental changes in potency, solubility, and reaction scope, which may be insufficient for modern applications wanting sharper physicochemical property control. The 2,4-difluoro substitution brings a step-change: it lowers electron density uniformly across the aromatic ring, enhances robustness under harsh conditions, and, in some cases, blocks undesired metabolic breakdown pathways in biological systems.

    Process engineers gravitate toward this intermediate because it supports high yields, even with challenging coupling partners. It holds up under sustained heat and variable pH ranges without deacetylating unexpectedly. These properties prove essential in batch and continuous flow chemistry, where reaction control needs to be predictable and waste needs to be minimized for cost and environmental reasons.

    Environmental and Compliance Considerations

    No chemical can be considered in isolation from the expectations of modern industry standards. Our plant operations meet strict environmental compliance guidelines. We recover and recycle solvents from our 2,4-difluoroacetanilide lines and treat waste streams in closed systems. Real-world sustainability goes beyond paperwork. Persistent fluorinated waste can present a challenge if not managed from the start, so we continually seek catalysts or alternative workups to reduce potential downstream residue.

    Regulatory requests—from responsible sourcing documentation to detailed impurity profiles—surface more frequently as downstream products approach registration. Our dedicated quality and compliance team maintains full transparency, offering customers and regulators coherent documentation linking every batch back to source data and safety assessments. Working in the field shows us that ongoing, direct feedback from inspection teams keeps our program honest and up to the mark.

    Continuous Improvement Drives Results

    Seeing the evolution of specifications over the years, often in response to new analytical technology or shifting regulatory focus, encourages a culture of data-driven improvement. Investing in advanced chromatography and in-line monitoring lets us track batch consistency in real time. Even small shifts in impurity patterns receive attention, as these can foreshadow scale-up risks or later product instability.

    Our operators and technical managers frequently cross-train and audit each stage—from raw material incoming checks through to drum loading. Working hands-on with each product day in, day out, team members know how 2,4-difluoroacetanilide behaves across seasons, humidity, and storage conditions—experience gained only by years of close involvement. These insights lead to innovations in packaging, smarter inventory rotation, and faster responses should quality issues ever arise.

    Solutions to Common User Challenges

    Chemists in the laboratory often ask about storage and handling, having heard stories of moisture pickup or slow degradation affecting similar fluorinated intermediates. We recommend airtight, inert atmosphere storage and offer guidance on safe sampling techniques. Our own experiences confirm that rapid capping and desiccant protection make a difference, especially in humid climates or where bench operations occur over several shifts.

    Another frequent inquiry concerns scale-up. Transitioning from gram-scale trial runs to kilogram or ton quantities reveals sometimes unexpected changes—different stirring effectiveness, slower dissolution rates, or uneven crystal formation. Our scale-up teams approach these transitions by running small pilot batches, testing the influence of mixing speed, and checking for subtle changes in impurity formation. Problems that surface at these stages—such as colored impurities or variations in melting point—lead us to refine both upstream reaction and downstream purification steps.

    Users operating continuous flows rather than batch reactors sometimes face solvent compatibility questions. The hydrophobic nature of the difluorinated structure can require solvent optimization to guarantee complete dissolution and consistent feed rates. Through extensive in-plant testing, we share solvent recommendations and pre-dilution protocols to support hassle-free integration into diverse synthetic regimes.

    Delivering Trust Through Experience

    Looking at the demands on today’s specialty chemical supply chain, steadfast reliability defines long-term partnerships. The success of our 2,4-difluoroacetanilide production reflects decades refining aromatic fluorination chemistry, safety, and logistics management. Each shipment demonstrates our ability to anticipate and address the challenges users actually encounter on the bench and in full-scale reactors.

    Manufacturing is more than process optimization; it is a commitment to empowering downstream innovation and responsible practice. We see 2,4-difluoroacetanilide as one key part of this larger effort—supporting safer, more effective products that enter markets around the world.

    Moving Forward—Collaboration and Innovation

    Meeting evolving industry goals means deepening our expertise and staying engaged with chemists, engineers, and regulatory teams. As researchers push for new applications—whether in targeted pharmaceuticals, specialty agrochemicals, or advanced materials—direct feedback shapes both day-to-day operations and long-term R&D. New downstream requirements, alternative synthetic strategies, and shifting compliance expectations drive us to adapt and refine the way we work with this intermediate and every other complex building block we produce.

    The lessons learned from years in the field—troubleshooting unexpected reactivity, managing sensitive logistics, supporting compliance audits—feed directly into our processes and policies. These experiences, grounded in actual production, set the foundation for confident supply and trusted partnerships. Our manufacturing journey with 2,4-difluoroacetanilide stands as ongoing proof that knowledge from experience delivers results the market can rely on.