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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
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    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

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    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.