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3,6-Difluorophthalic Anhydride

    • Product Name 3,6-Difluorophthalic Anhydride
    • Alias 3,6-Difluoro-1,3-isobenzofurandione
    • Einecs 700-935-0
    • 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
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    Specifications

    HS Code

    779814

    Chemical Name 3,6-Difluorophthalic Anhydride
    Molecular Formula C8H2F2O3
    Molecular Weight 184.10 g/mol
    Cas Number 401-76-3
    Appearance White to off-white solid
    Melting Point 178-181 °C
    Density 1.65 g/cm³ (calculated)
    Solubility Reacts with water, soluble in organic solvents such as acetone, chloroform
    Purity Typically ≥98%
    Smiles O=C1OC(=O)c2c(C1)cc(F)cc2F
    Storage Conditions Store in a cool, dry, well-ventilated area, protected from moisture
    Hs Code 2917.39
    Synonyms 3,6-Difluoro-1,3-isobenzofurandione

    As an accredited 3,6-Difluorophthalic Anhydride 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, sealed with a plastic screw cap, labeled with hazard warnings and product details for 3,6-Difluorophthalic Anhydride.
    Shipping 3,6-Difluorophthalic Anhydride is shipped in tightly sealed containers to prevent moisture and contamination. It should be stored and transported in a cool, dry, and well-ventilated area. Proper labeling, hazard documentation, and adherence to local regulations are required, as the chemical may be an irritant and requires careful handling.
    Storage 3,6-Difluorophthalic Anhydride should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from moisture and incompatible substances such as strong bases and oxidizers. Avoid exposure to air and humidity to prevent hydrolysis. Store under inert atmosphere if possible, and clearly label the container. Protect from physical damage, heat, and direct sunlight.
    Application of 3,6-Difluorophthalic Anhydride

    Applications of 3,6-Difluorophthalic Anhydride in Industrial Manufacturing

    3,6-Difluorophthalic anhydride serves as a specialized intermediate in high-value industrial sectors. Our production integrates advanced fluorination and purification techniques to ensure consistent quality for critical downstream applications. Below are key industry scenarios where this material delivers unique technical and compliance advantages.

    1. High-Performance Polyimide Films for Electronics

    Electronics manufacturers incorporate 3,6-difluorophthalic anhydride as a comonomer for synthesizing fluorinated polyimides. These polyimides show superior dielectric properties and high thermal stability, essential for flexible printed circuits, high-density interconnects, and display substrate films. Integrating this monomer enhances transparency and reduces water absorption in polyimide matrices, critical for next-generation flexible device architectures.

    Industry compliance standards

    • RoHS Directive (2011/65/EU) for electronic device components
    • REACH Regulation (EC 1907/2006) for registration and authorization
    • UL 94 flammability testing for polymers
    • IPC-4101E for base materials in PCB substrates

    Typical usage ratio

    • 10–30 mol% of total dianhydride content, with exact levels adjusted to target dielectric and mechanical performance requirements

    Downstream process integration

    • Direct addition during polyamic acid synthesis step, followed by thermal imidization in polyimide film casting operations

    Final product types

    • Flexible printed circuit boards
    • Transparent polyimide display films
    • Flexible copper-clad laminates
    • Microelectronic packaging materials

    2. Specialty Fluorinated Polyesters for Optical Applications

    Specialty polymer manufacturers use 3,6-difluorophthalic anhydride to synthesize high-refractive-index polyesters. The fluorine atoms lower dielectric loss and enhance optical transmittance, supporting the production of light-guiding films, lenses, and polarizer substrates. The incorporation of this anhydride enables adjustment of film flexibility and clarity, balancing mechanical durability with advanced optical requirements.

    Industry compliance standards

    • ISO 8980 for ophthalmic optics and lens spectacle lenses
    • EN 166 for personal eye protection
    • RoHS compliance for electronics-related optical components
    • ASTM F2824 for optical film properties

    Typical usage ratio

    • 8–20 wt% of total acid component in polyesterification, modulated according to refractive index and transmission needs

    Downstream process integration

    • Co-monomer stage in melt polycondensation with corresponding diols under controlled vacuum and temperature

    Final product types

    • Optical grade thin films
    • Flat panel display filters
    • Optical lenses (eg. camera, wearable, and sensor lenses)
    • Light guide plates for LED applications

    3. Engineering Plastics for Chemical-Resistant Parts

    Producers of high-performance engineering plastics blend 3,6-difluorophthalic anhydride as a functional modifier in resins to impart enhanced fluorine-derived chemical resistance. This is critical in pumps, seals, and valve components for chemical processing or semiconductor wet benches, where aggressive fluids and purity demands are stringent. The anhydride enables fine-tuning of polymer chain rigidity and hydrophobicity.

    Industry compliance standards

    • ASTM D543 for plastic chemical resistance
    • UL 746C for polymeric material performance
    • ISO 10993-5 for cytotoxicity in plastics with potential human contact
    • ISO 1043-4 fluorinated plastic identification and labeling

    Typical usage ratio

    • 5–15 mol% of total anhydride or acid components, adjusted for mechanical and resistance properties required by application

    Downstream process integration

    • Direct feeding with other monomers or modifiers into twin-screw extruder or bulk polymerization reactor for base resin synthesis

    Final product types

    • Chemical pump impellers
    • Valve housings and seals
    • Semiconductor wet process trays
    • Battery component housings

    4. Heat-Resistant Coatings for Aerospace and Automotive

    Formulators in coating industries use 3,6-difluorophthalic anhydride in polyimide-based or fluorinated resin systems to boost thermal and weathering resistance. This approach suits exterior coatings for aerospace components, automotive engine enclosures, and high-temperature insulation materials. The fluorinated backbone improves UV tolerance and long-term dimensional stability without sacrificing adherence or flexibility.

    Industry compliance standards

    • SAE AMS 3132 for high temperature resistant coatings
    • ASTM D3029 for electrical insulation coatings
    • ISO 9227 for corrosion testing under saline environments
    • MIL-PRF-22750 for aircraft component coatings

    Typical usage ratio

    • 15–25 mol% in copolymer resins, with precise dosage determined by aging, gloss retention, and exposure cycle requirements

    Downstream process integration

    • Combined with other dianhydrides or diacids in prepolymer solution, followed by spray, dip, or roll coating and final curing through imidization or crosslinking

    Final product types

    • Aerospace structural coatings
    • Automotive engine bay finishes
    • Industrial-grade insulating varnishes
    • Protective coatings for electronics enclosures

    5. Liquid Crystal Polymer (LCP) Monomer for Advanced Electronics

    Material scientists in LCP production select 3,6-difluorophthalic anhydride to synthesize semiflexible rod-like copolymers. These LCPs offer high-temperature resistance, low dielectric loss, and processability for high-frequency connectors, 5G antenna components, and chip packaging substrates. The presence of difluorinated units facilitates molecular alignment, optimal for micro-patterned circuit fabrication.

    Industry compliance standards

    • IPC-4103C for LCP-based base materials
    • IEC 61249-2-51 for halogen-free laminates
    • ISO 9001:2015 for quality management systems in electronics
    • RoHS restriction for halogen content in final assemblies

    Typical usage ratio

    • 10–30 mol% in copolymer backbone, defined by melt index, operating frequency range, and other electrical properties

    Downstream process integration

    • Introduce as dianhydride or bis-acid component during polycondensation with hydroquinone or biphenols, followed by injection molding or extrusion

    Final product types

    • High-frequency connector housings
    • Microwave circuit substrates
    • Thin-film LCP circuit carriers
    • 5G and RF device modules

    6. Advanced Dye Intermediates for Technical Textiles

    Fine chemical companies utilize 3,6-difluorophthalic anhydride as a key intermediate in synthesizing fluorinated dyes for technical textiles. These dyes exhibit high fastness and reduced surface energy, which impart improved stain andwater repellency to polyester, nylon, and aramid fabrics. The raw material’s electron-withdrawing fluorine functionality enhances dye bonding and weathering stability, especially for protective and industrial garments.

    Industry compliance standards

    • OEKO-TEX Standard 100 for restricted substances in textiles
    • REACH SVHC compliance for hazardous substances
    • ISO 105 series for color and wash fastness
    • ZDHC MRSL for safer chemical management

    Typical usage ratio

    • Secondary aromatic acid component at 5–18 mol% within the dye molecule core, depending on polymer substrate reactivity and desired fastness profile

    Downstream process integration

    • Participates in condensation with amine chromophores, followed by sulfonation or alkylation, and then final powder isolation and dispersing for textile dyeing baths

    Final product types

    • Water-repellent fabric dyes
    • High-washfast synthetic textile colorants
    • Technical apparel and uniform dyes
    • Outdoor equipment fabric treatments
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    Certification & Compliance
    More Introduction

    3,6-Difluorophthalic Anhydride: A Closer Look from the Manufacturer’s Perspective

    Understanding the Material

    Over the last decade, we have noticed a growing interest in specialty anhydrides and 3,6-Difluorophthalic Anhydride consistently finds its way into the conversations about advanced polymers. In practical terms, its unique difluoro-substitution on the aromatic ring makes it a go-to for chemists aiming for both thermal stability and improved electronic properties within a mid-range phthalic anhydride derivative. This isn’t just a claim from a glossy brochure — experience in the reactor hall has shown that these small differences in molecular structure have significant consequences on the performance of the polymers built from them.

    Our model, identified simply as 3,6-DFPA, typically appears as a fine white to off-white powder, though larger-scale customers often request specific particle size tuning for easier handling in bulk operations. Measured purity remains consistently above 99%, and we maintain rigorous controls in production to avoid halogen contamination, which can otherwise wreak havoc in downstream applications, particularly electronics.

    Application Insights: What the Molecule Really Delivers

    In the lab, 3,6-Difluorophthalic Anhydride takes on multiple roles. Ingredient requests from polyimide manufacturers have increased as the electronics industry pushes toward lighter, stronger, yet flexible substrates. Polyimides built from our anhydride exhibit a marked increase in dielectric strength, and they show less weight gain when exposed to moisture, a factor that matters as circuit density keeps climbing. This is not mere specification board talk: one customer in the flexible display market reported that their yields jumped after switching to a formulation containing our product as a comonomer, citing both improved product stability and ease of patterning.

    We often supply to the coatings sector, where color fastness and resistance to environmental degrade matter over the long haul. Many color developers, especially in red and orange pigments, opt for our 3,6-DFPA because it resists photobleaching much better than non-fluorinated or mono-fluorinated analogues. This resistance comes from the unique C-F bonds, which absorb less UV energy than other functional groups, translating to longer-lasting appearance in exposed parts. Some end users in automotive coatings told us a direct cut in warranty claims followed the switch to formulations using our anhydride.

    Why Choose the 3,6-Difluoro Variant?

    One question we field at trade shows comes from process technologists asking how 3,6-DFPA stands apart from standard phthalic anhydride or mono-fluorinated versions. The immediate answer: this specific difluoro arrangement balances reactivity with durability. Standard phthalic anhydride offers baseline functionality, but struggles in applications where exposure to heat or chemicals is the norm. Mono-fluorinated types improve performance but do not match the thermal and chemical durability reported with the 3,6-configuration. Importantly, the difluoro derivative also shows less byproduct formation in imidization steps, a feature valued by quality-driven polyimide manufacturers who count on high conversion rates and fewer purification cycles.

    In our production environment, the challenge comes down to controlling undesired isomers and minimizing difluorinated impurities at non-3,6 positions. Years spent refining the synthesis route have given us reliable, scalable processes — not just for academic samples, but for commercial metrics where tonnage and repeatability matter. Raw material purity and temperature control contribute directly to the consistently high isolation yields we achieve, which in turn affect the economics and usability for our downstream partners.

    Specifications and Technical Points Worth Considering

    We field requests for particle analysis, thermal decomposition profiles, and melt flow characteristics almost daily. For this compound, the melting point sits above that of standard phthalic anhydride, which translates to added thermal margin in final polymers. Glass transition and decomposition behaviors, as measured by differential scanning calorimetry and thermogravimetric analysis, frequently become focal points in project-specific discussions — especially with customers scaling up for electronic substrates. Most of our batches show TGA mass loss onset at temperatures comfortably above 300°C. We monitor any residue formation since this can complicate downstream processing, and by focusing on lot-to-lot consistency, we give researchers confidence in reproducibility.

    It bears noting that, in practice, polyimides incorporating 3,6-DFPA offer performance improvements that are not always obvious from standard material data sheets. In-use testing reveals reduced outgassing under vacuum, a feature that satellite and aerospace firms, in particular, value highly. We’ve even had clients run atomic oxygen exposure tests — results have been encouraging, showing fewer failures and surface degradation events than parallel composites based on older anhydrides. This isn’t a theoretical improvement; our technical support team works alongside customers to integrate feedback directly into our process control system, closing the loop between the bench and the plant.

    Experience with Handling, Safety, and Process Compatibility

    Bulk manufacturing of 3,6-DFPA brings its own lessons. The anhydride functional group gives off a characteristic odor; experienced operators recognize it right away, and that has real implications for plant ventilation and operator PPE practice. Early pilot runs taught us the limits of existing dust collection systems, so we invested in upgrades years before regulatory mandates began catching up across several regions. One item worth sharing: even a marginal rise in atmospheric moisture can trigger unwanted partial hydrolysis, so we pack our product under dry nitrogen and ship in double-sealed drums. Not every client prioritizes these steps, but feedback from those in humid environments confirms their effectiveness.

    We also share knowledge on storage because improper conditions can kill reactivity before a batch even hits the process tank. Our QC group runs accelerated aging studies on retained samples, giving real timelines for workable shelf life under typical warehouse conditions instead of the outsized promises sometimes seen in generic documents. These practices aren’t just about covering ourselves; we see fewer customer complaints and better process yields in plants where the chain of custody is clearly maintained.

    Competing Products and Their Limitations

    One popular query comes from formulators weighing 3,6-DFPA against alternatives. Non-fluorinated phthalic anhydrides come in cheaper, but deliver a lower stability ceiling under electrical or chemical load. Polyimides built from these alternatives tend to yellow and degrade faster, which leads to frequent maintenance or warranty exposure in critical end-use markets. Mono-fluorinated derivatives, particularly those with the fluorine at the 4-position, tend to underperform on hydrolytic resistance and do not suppress dielectric loss as effectively.

    What often goes unsaid in published studies is that trace impurities from off-spec isomer formation or incomplete conversions bleed into downstream operations. This matters for those in pharmaceutical and electronics fields, where even small process inconsistencies can lead to rejected lots. We’ve invested heavily in inline analytical tools and partner with suppliers to push the envelope on incoming raw material screening. Year over year, we see fewer issues with lot variability and customer feedback backs up this approach: tighter controls upstream equal fewer headaches downstream.

    Field Problems and Solutions: Real-World Chemistry Lessons

    Every manufacturer faces setbacks in scaling up from laboratory-scale synthesis. Solvent recovery and fluorine management become immediate bottlenecks when running larger reactors. Some years back, unplanned downtime triggered by contamination in a distillation run forced our process team to revise cleaning protocols and invest in higher-grade seals for our reactors. These upgrades now serve us — and our customers — by minimizing cross-contamination and ensuring that each lot leaves the plant with minimal residual byproducts.

    Packaging, too, has seen three revisions in the last five years. Direct feedback from a large electronics client in a tropical climate showed that the classic steel drum approach failed to maintain product integrity over long sea voyages. After reviewing transit conditions, we shifted to a laminated barrier liner system which, while more expensive, completely eliminated hydrolysis-related failures. Customers in Vietnam and Thailand have since reported consistently better results after switching. Such changes can’t be captured on a traditional spec sheet, but they make a visible difference in end-use performance.

    Supporting Responsible Manufacturing

    Environmental factors can’t be an afterthought. Fluorinated compounds invite regulatory scrutiny regarding their impact on air and water systems. We deploy scrubbers on all exhaust streams that might carry organofluorine residues. Our water treatment facility uses activated carbon beds and advanced oxidation, reducing fluorine waste well below emission thresholds. Technical teams continuously update our compliance protocols, both to satisfy regulatory updates in North America and Europe and to anticipate evolving standards across Asia.

    On the worker safety front, we perform regular skin-residue tests for line operators and invest in PPE training beyond compliance checklists. Production veterans know that even a trace of fluorinated acid contamination leads to longer-term corrosion in shared process equipment, so our plant maintenance schedule includes quarterly deep cleans rather than annual overhauls. These steps translate to fewer incidents, higher morale, and a stronger product reputation in the marketplace.

    The Value of Manufacturer-Driven Technical Support

    Customers developing new formulations with 3,6-Difluorophthalic Anhydride often call for data or suggestions beyond what paperwork supplies. We see technical support not as an afterthought, but as a core service. Application scientists regularly field troubleshooting calls on imidization times, solvent selection, or compatibility with co-monomers. In one case, a client experienced unexpected crosslinking artifacts. After reviewing process details, we recommended a minor adjustment in process pH and drying protocols, which fixed the product issue and restored throughput. This sort of dialogue forges relationships beyond simple supply contracts.

    We take part in industry working groups and contribute anonymized trends to global benchmarking efforts. Our participation means clients can lean on real-world experience, not just chemical theory. Most line chemists want to know what worked — and what failed — in other facilities. Sharing that know-how reduces costly mistakes and smooths the entry of new compounds into high-stakes, high-value applications.

    Market Trends and What They Mean for the Future

    Each year, demand for advanced electronics and specialty coatings ticks upward, and so does our order book for 3,6-DFPA. Lightweight, flexible, and stable polymers are in demand across 5G infrastructure and high-reliability automotive modules. Asian manufacturers, historically relying on local mono-fluorinated or non-fluorinated feedstocks, are increasingly turning to higher-performance options as their own markets demand better reliability. Our experience tells us this trend is unlikely to reverse; small differences in upstream chemistry create large differences in downstream profitability.

    Rising regulatory focus on fluorine-containing substances has spurred investment in cleaner, more efficient synthesis routes. We adopt closed-loop systems and continuous processing lines wherever possible to cut waste. Not every solution is glamorous, but incremental change keeps us ahead of both performance and regulatory requirements.

    Conclusion: Lessons from the Production Line

    Working as a manufacturer gives unique perspective on what makes 3,6-Difluorophthalic Anhydride valuable. Its performance edge, whether in polyimide substrates or long-lasting pigment dispersions, rests on plant-level discipline and a commitment to hearing what end users really need. Lessons gathered from retooling production lines, adapting packaging, and answering urgent technical calls all feed back into how we refine both product and process. When customers visit our plant or review delivery records, they see the result of real-world problem solving — not just molecular diagrams or generic quality claims.

    We keep listening, adapting, and improving, because the demands set by next-generation electronics, coatings, and composite applications keep rising. Those same pressures drive every improvement, every technical tweak, and every new piece of advice we offer. That’s the reality of manufacturing specialty chemicals in a world that demands both performance and responsibility.