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

3,6-Dibromophthalic Anhydride

    • Product Name 3,6-Dibromophthalic Anhydride
    • Alias DBPA
    • Einecs 221-801-7
    • 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
    VTB
    Specifications

    HS Code

    750868

    Chemical Name 3,6-Dibromophthalic anhydride
    Cas Number 36568-50-4
    Molecular Formula C8Br2O3
    Molecular Weight 339.89 g/mol
    Appearance White to off-white solid
    Melting Point 251-254 °C
    Boiling Point Decomposes before boiling
    Solubility Slightly soluble in water; soluble in organic solvents
    Density 2.54 g/cm³
    Purity Typically >98%
    Synonyms 3,6-Dibromo-1,3-isobenzofurandione
    Storage Conditions Store in a cool, dry place, tightly closed
    Inchi Key NZZXSRQZZHESKH-UHFFFAOYSA-N
    Hazard Classification Irritant

    As an accredited 3,6-Dibromophthalic Anhydride factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing
    Shipping
    Storage
    Application of 3,6-Dibromophthalic Anhydride

    Applications of 3,6-Dibromophthalic Anhydride in Industrial Manufacturing

    As a direct manufacturer of 3,6-Dibromophthalic Anhydride, we enable precise integration of this specialized intermediate into formulations where advanced molecular structure and halogen content are required. Our material supports several defined industrial value chains by supporting high-performance requirements in specific end-use production systems. Below is a detailed breakdown of its recognized roles across authentic downstream application segments.

    1. High-Temperature Resistant Polyimide Materials

    Polyimide manufacturers utilize 3,6-Dibromophthalic Anhydride as a halogenated dianhydride building block for imide monomer synthesis, introducing controlled bromine content for flame retardancy in thermoset polyimide films and parts. The anhydride reacts with diamines via one-step or two-step polycondensation methods, enhancing flame resistance without compromising mechanical integrity or thermal stability. The precise introduction step and quality control measures play a critical role in the dielectric and safety properties of the cured polyimide product.

    Industry compliance standards

    • UL 94 (Flammability Testing for Plastics)
    • IEC 60384 (Fixed Capacitors for Use in Electronic Equipment)
    • JPCA-ES-01 (Japan Electronics Packaging and Circuits Association Guidelines)
    • REACH Regulation Annex XVII (Halogenated Flame Retardants)

    Typical usage ratio

    • 8%–25% by mass of total dianhydride content, adjusted based on required flame retardancy and processing viscosity

    Downstream process integration

    • Reacted with aromatic diamine monomers during initial polyamic acid synthesis stage, followed by thermal imidization under controlled conditions

    Final product types

    • Wire and cable insulation films
    • Flexible printed circuit board base films
    • Insulation tapes for high-temperature motors and transformers
    • Automotive electronics protective laminates

    2. Halogenated Dye Intermediates for Specialty Pigments

    Producers of high-performance dyes and pigments use 3,6-Dibromophthalic Anhydride as a core halogenated anhydride intermediate to synthesize brominated phthalimide derivatives. These downstream intermediates enable the formation of anthraquinone and perylene-based pigments with improved fastness and shade depth, particularly suited for plastics and industrial coatings. During the condensation process, the anhydride’s electron-donating and steric effects contribute to color intensity and dispersion, with strict process monitoring to minimize impurities that affect hue or stability.

    Industry compliance standards

    • EN 71-3 (Toy Safety – Migration of Certain Elements, for dyestuff in toys and coatings)
    • ETAD Code of Practice (International Association of the Colorants Industry)
    • OEKO-TEX® Standard 100 (Textile and Leather Chemicals, Pigment Additives)
    • REACH Annex XVII (Aromatic Amines Restrictions)

    Typical usage ratio

    • 12%–30% molar proportion in phthalimide-based dye synthesis; value determined by pigment type and target properties

    Downstream process integration

    • Condensed with amino-aromatic or cyano compounding reactants during the core pigment synthesis step under temperature-controlled conditions

    Final product types

    • High-performance plastic colorants
    • Industrial paints and coatings for outdoor metallic surfaces
    • Automotive OEM pigments
    • Heat-resistant print ink bases

    3. Flame Retardant Additive Synthesis for Engineering Resins

    Manufacturers of bromine-based flame retardant additives incorporate 3,6-Dibromophthalic Anhydride as a controlled halogen donor in the production of additive masterbatches and blended resins. The anhydride enters the synthesis of reactive and additive-type retardants suited for engineering plastics such as polybutylene terephthalate and polycarbonate. The resulting brominated compounds are then melt-compounded with thermoplastics or directly used in compounding lines, imparting non-migratory flame resistance while minimizing the impact on mechanical properties and processability.

    Industry compliance standards

    • UL 94V (Vertical Burning Test for Plastics)
    • RoHS Directive 2011/65/EU (Restriction of Hazardous Substances in Electrical and Electronic Equipment)
    • IEC 60695-11-10 (Fire Hazard Testing for Flames)
    • ISO 1043-4 (Plastics — Symbols and Abbreviations — Flame Retardants)

    Typical usage ratio

    • 3%–15% by weight in finished flame retardant additives for further compounding, varied as per resin matrix and required fire performance class

    Downstream process integration

    • Incorporated during flame retardant additive synthesis (typically by esterification or imide formation) prior to extrusion and pelletizing with resin bases

    Final product types

    • Flame retardant masterbatches for engineering plastics
    • Blended flame retardant thermoplastic pellets
    • Compounded resins for electrical appliance housings
    • Construction-grade plastic building elements

    4. Special Epoxy Resin Curing Components

    Producers of specialty epoxy resins for electronics and encapsulation utilize 3,6-Dibromophthalic Anhydride as a multifunctional anhydride curing agent delivering both enhanced thermal stability and flame index. This raw material supports the synthesis of advanced anhydride hardener blends for precise crosslinking in castings, potting compounds, and PCB substrates, reducing halogen migration and optimizing electrical insulation. The anhydride enters the ingredient mixing stage of epoxy formulation, where operators control stoichiometry and curing profile to ensure batch uniformity for downstream assembly lines.

    Industry compliance standards

    • IPC-4101 (Specification for Base Materials for Rigid and Multilayer Printed Boards)
    • UL 94-5V (Flame Class for Epoxy Laminates)
    • IEC 61249-2-21 (Halogen-Free Laminate Requirements for PCBs)
    • ISO 9001 (Quality Management for Composite Materials Manufacturing)

    Typical usage ratio

    • 10%–35% of total anhydride curing component by mass, with adjustments based on resin epoxide equivalent weight and targeted gel/cure profile

    Downstream process integration

    • Directly blended with base epoxy resins during premix, followed by thermal or catalytic curing in vacuum molds or continuous lamination systems

    Final product types

    • Electronic encapsulant resins for semiconductor devices
    • PCB substrate laminates and prepregs
    • Electrical potting compounds
    • High-heat resistant structural adhesives

    5. Advanced Perylene Dye Synthesis for High-Performance Plastics

    Chemical companies focused on perylene-based dye systems employ 3,6-Dibromophthalic Anhydride as a targeted halogenated building block in the stepwise synthesis of perylene tetracarboxylic dianhydrides and their derivatives. The anhydride participates in condensation and cyclization reactions that directly impact the final product’s stability, lightfastness, and heat resistance, especially relevant for high-performance plastic coloration where pigment migration and color fade pose major technical challenges.

    Industry compliance standards

    • FDA 21 CFR 178.3297 (Pigment Use in Food Contact Plastics, United States)
    • ISO 18451-1 (Pigments and Extenders – Terminology Guidelines)
    • DIN EN 12877-1 (Colourants for Plastics – Safety Requirements)
    • REACH registration for industrial pigment applications

    Typical usage ratio

    • 10%–22% mole equivalent during perylene core construction; ratio tailored for target molecular uniformity and application requirements

    Downstream process integration

    • Reacted in high-temperature closed condensing reactors during the core dye-building process before further functionalization or salt formation

    Final product types

    • Perylene-based color masterbatches
    • Polycarbonate and polyamide molded parts with intense coloration
    • Fiber-grade pigments for high-strength synthetic textiles
    • UV-resistant outdoor plastic components

    6. Performance Additives for Specialty Coatings

    Coatings formulators integrate 3,6-Dibromophthalic Anhydride as a core intermediate in synthesizing halogen-containing additives for advanced coating systems that demand both fire resistance and weather durability. The material enters the synthesis of curing agents or polymer binders for industrial coatings, particularly those applied on electronic housings, transport equipment, or infrastructure surfaces requiring sustainability under thermal load and exposure. Process engineers carefully measure and introduce the anhydride during pre-polymer or additive synthesis to finely adjust the reactivity and performance of the end formulation.

    Industry compliance standards

    • ASTM D3273 (Standard Test Method for Resistance to Growth of Mold on Coating Films)
    • EN 13501-1 (Fire Classification of Construction Products and Building Elements)
    • ISO 12944 (Corrosion Protection of Steel Structures by Protective Paint Systems)
    • Directive 2004/42/EC (VOC Content in Decorative Paints and Varnishes)

    Typical usage ratio

    • 5%–18% by polymer or additive precursor weight, modulated by targeted fire performance and applied film thickness

    Downstream process integration

    • Synthesized into binder or additive matrix before crosslinker/additive blending and final paint dispersion

    Final product types

    • Fire-retardant architectural coatings
    • Protective marine and industrial topcoats
    • Specialty automotive paints with high weatherability
    • Electronic device exterior protective layers
    Free Quote

    Competitive 3,6-Dibromophthalic Anhydride 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

    Introducing 3,6-Dibromophthalic Anhydride: Key Building Block in Modern Synthesis

    New materials drive innovation across countless industries, and chemistry rests at the crux of these efforts. Some compounds quietly shape the direction of research and industry thanks to their unique properties and reliability. 3,6-Dibromophthalic anhydride, sometimes listed with the model number DBPA or by its CAS number 2674-37-3, falls into this category. Its versatility uplifts it far above a simple reagent or intermediate. I've seen firsthand why specialists in dyes, polymers, and advanced materials turn to this anhydride time after time.

    The Structure Behind Success

    This crystalline white or pale yellow powder packs two bromine atoms right at the 3 and 6 positions of the phthalic anhydride core. Anyone who has sat in front of a mass spectrometer can appreciate what halogens bring: they adjust reactivity, shape electronic environment, and create new avenues in ring-opening reactions. This molecular design doesn’t just offer another halogenated anhydride—it carves a place in serious synthetic projects. The melting point sits high enough to ensure stability across standard storage and shipping. Well-dried conditions preserve the purity, with moisture exclusion essential to avoid hydrolysis in sensitive projects.

    Real-World Impact and Applications

    In my own lab work, finding the right anhydride can make or break the synthesis of performance polymers. With 3,6-dibromophthalic anhydride, researchers have opened doors in the world of polyimide resins. These polymers show up in everything from flexible electronics to aerospace-grade laminates. It stands out in the crowd—once reacted into the polymer backbone, those two bromine atoms don’t just fade away. They help shape flame resistance and make downstream reactions easier, including grafting and further modification.

    I have watched developmental teams reach for this molecule when traditional phthalic anhydride falls short. It isn’t just about adding “something different” to the backbone; it’s about targeting real challenges—heat resistance, chemical stability, precision in color shade for dyes, even the ability to participate in advanced coupling reactions. In the dye industry, for example, 3,6-dibromophthalic anhydride enables vibrant, lightfast pigments. Bromination boosts both the stability and intensity of color in these materials, providing tangible advantages over basic anhydrides or their chlorinated cousins.

    Points of Distinction: What Makes This Anhydride Special

    Anyone who has wrestled with reactivity issues knows that not all anhydrides perform the same way. Phthalic anhydride sits at the origin, a simple and accessible building block. Chlorinated or other halogenated analogues adjust the electron density in their own ways. The presence of bromines at positions 3 and 6 in 3,6-dibromophthalic anhydride has proven particularly valuable. The larger size and polarizability of bromine, compared to chlorine or fluorine, introduce subtler electronic effects. These tweaks pay off in end uses where precise control over substitution patterns is required.

    When comparing performance in high-temperature applications or where flame retardancy matters, I’ve seen users quickly recognize the value of this compound. It provides a robust alternative to both mono-halogenated and non-halogenated anhydrides, especially in settings where reproducible, fine-tuned reactions make or break project timelines. Brominated derivatives tend to offer more robust reactivity than their chlorinated cousins, reducing the need for harsh reaction conditions. This can lower the overall environmental burden and risk during process scale-up.

    Working with Professionals: Sourcing and Quality Assurance

    Anyone who has run large-scale reactions knows that the jump from academic to industrial grade brings tough questions. End users in electronics, pigment manufacturing, and advanced composites look for high purity—generally above 99 percent—and careful packaging. Batch certification, rigorous spectroscopic testing, and clear traceability go from nice-to-have to required features. Over the years, the market for 3,6-dibromophthalic anhydride has matured, but the savvy buyer can always differentiate based on transparency and track record.

    The specification most often requested is high purity, usually confirmed through HPLC, NMR, or even mass spectrometry in highly regulated industries. Moisture content checks and proper particle sizing matter as well, especially for high-precision applications where flow properties affect blending or dispersion, such as in powder coating manufacturing or resin blending. Impurities such as isomeric by-products or residual solvents can derail delicate dye syntheses or polymerizations. It’s become routine for suppliers to provide exhaustively documented certificates of analysis, and customers have grown more skilled at verifying these credentials.

    The years taught many buyers—including myself—that small changes in quality can ripple through an entire batch, impacting color stability, mechanical strength, or flame retardant performance. Unlike off-the-shelf goods, specialist chemicals demand more attention to purity, handling, and documentation. Certified storage conditions, desiccant-lined containers, and clarity about shelf life have become central to purchasing decisions for high-stakes projects.

    Shifting from Lab to Industrial Scale

    Researchers enjoy the freedom to experiment with small batches on the bench, but scaled-up production reveals hidden challenges. The bulk synthesis of polyimides using this anhydride sees plenty of questions: how to keep reaction yields high, how to reach consistent molecular weights, and how to integrate additional functional groups post-polymerization. This anhydride’s particular strengths—bromine’s role as a chemical handle and its fire-retarding effects—ease the transition. Past projects demonstrated that end results often outperform similar products made with plain phthalic anhydride or even some dichloro analogues.

    Supplier relationships become even more vital at industrial scale. Inconsistencies or variable batch purity can bring entire production lines to a halt. Long-term partnerships have led many end users, ranging from aerospace firms to small pigment houses, to choose tried-and-tested sources of 3,6-dibromophthalic anhydride. Over time, this stability has enabled more daring research projects, knowing that material quality will remain constant from gram to ton scale. Logistics reliability—timely delivery, real-time inventory feedback—also plays a role for those managing continuous production with little room for error.

    Addressing Environmental Considerations

    Every chemist confronts the environmental stakes of their material choices. Brominated compounds spark debate due to their persistence and, in some cases, potential toxicity. The difference between 3,6-dibromophthalic anhydride and widely criticized classes of flame retardants lies in its application and structure. Instead of free, mobile bromines readily leaching out, the molecule’s design allows downstream fixation as part of stable, high-molecular-weight polymers.

    Still, users treat disposal with caution, adhering to established chemical waste protocols. The growing popularity of closed-loop processes and recovery systems in polymer manufacturing echoes the entire sector’s push for greener chemistry. I have followed companies who invest in solvent reclamation and product recovery, minimizing overall waste and protecting the water table from halogenated runoff. Choosing to use this anhydride comes with responsibility, but also the potential for cleaner, safer processes compared to alternatives that demand stronger acids, heavier metals, or generate more toxic by-products.

    Comparing to Other Modified Anhydrides

    The debate between different halogenated phthalic anhydrides carries both cost and performance implications. Some users opt for mixtures of mono- and di-halogenated variants, trying to balance price and function. Yet in high-end electronics, advanced coatings, or where precision coloring matters, the distinct substitution pattern and purity of 3,6-dibromophthalic anhydride deliver better results. The material resists hydrolytic breakdown under moderate humidity, outpacing some chlorinated varieties that can suffer unwanted side reactions.

    Price points have narrowed over the past decade as production technologies improved. Still, the cost of errors—lower flame retardancy, color drift, inconsistent polymer properties—often outweighs minor per-kilo price differences when advanced performance is needed. Whether driving a base resin for flexible printed circuits, or building next-generation organic electronics, users report greater product consistency with the dibromo derivative. These results don’t simply come from academic literature—they reflect collective years of manufacturing experience and repeat testing.

    Guidance for Safe Use and Handling

    Working with halogenated anhydrides challenges even seasoned staff. Protective gloves, dust masks, good ventilation, and moisture-proof storage prove non-negotiable in most settings. In my years working with specialty chemicals, I’ve seen solid training make all the difference. Proper labeling, clear SOPs, and robust cleanup reduce risk for workers and facilities. Many organizations now bundle basic industrial hygiene with chemical-specific training modules, reviewing both regulatory compliance and hands-on procedure improvements.

    Chemical users sensibly avoid eating, drinking, or smoking in handling areas. Waste disposal always proceeds according to regulations, with all solvents and residues directed to control systems or licensed waste handlers. Those transferring or blending 3,6-dibromophthalic anhydride safeguard their process from static and moisture, storing the product in sealed, desiccated drums. Monitoring for dust or particulate emissions prevents secondary exposures, especially in settings close to other sensitive processes. Sharing lessons learned during internal audits has improved outcomes throughout the industry, keeping accident rates low even in demanding environments.

    Planning for emergencies means keeping access to showers, eyewash stations, and spill kits. Teams practicing regular drills recover more quickly in case of accidental exposures or material spills. Documentation trails—batch IDs, usage logs, waste manifests—help organizations understand their risk profile and show compliance during inspection. These habits do more than comply with regulation; they foster a safer, more reliable workplace across all points of contact.

    Innovation and Future Directions

    As technology and regulations evolve, users of 3,6-dibromophthalic anhydride face both opportunity and responsibility. Chemistry’s future will focus even more closely on environmental impact, material recyclability, and circular manufacturing. Polymer research is pushing toward high-performance resins that can be re-engineered or reused after their first life is done. The brominated backbone of this anhydride unlocks new initiatives in creating recoverable laminates or flame-resistant composites that can also be safely processed at end-of-life.

    Pigment scientists are testing extended color ranges, seeking more sustainable sources and less toxic co-reactants. Electronics developers depend on the material’s ability to enhance dielectric and flame-resistant properties at the sub-micron scale, especially important for miniaturized devices. New synthetic routes—using safer, greener solvents and lower energy—have begun to emerge, with some labs adopting continuous-flow microreactors for process intensification.

    Looking further ahead, demand for “greener” brominated anhydrides will shape both sourcing and end-of-life plans. Companies setting up stewardship programs, offering take-back schemes, or tracking cradle-to-grave metrics will find themselves poised to lead. Professional associations support these developments by providing clear guidance, investing in research consortia, and sharing best practices for safer, more efficient chemical use.

    A Material Rooted in Expertise

    It is easy to overlook niche compounds in the rush for new, flashier chemicals or dramatic breakthroughs. Yet, time and again, 3,6-dibromophthalic anhydride has shown it can deliver steady, dependable performance where it counts. Whether you work in dyes, polymers, specialty coatings, or electronics, the lessons of experience say: success relies not just on novelty, but on the careful balance of reactivity, safety, and system-level compatibility. In tough projects, the value lies not in extravagant claims, but in years of research, hard-won process improvements, and the consistency that this material brings to the table. Building out new materials based on reliable, well-studied intermediates sets the stage for safer, more sustainable, and more innovative industries in the years to come.