|
HS Code |
863725 |
| Product Name | 2,5-Dibromoterephthalic Acid |
| Cas Number | 27835-71-8 |
| Molecular Formula | C8H4Br2O4 |
| Molecular Weight | 339.93 g/mol |
| Appearance | White to off-white powder |
| Melting Point | Over 300°C (dec.) |
| Purity | Typically >98% |
| Solubility In Water | Slightly soluble |
| Boiling Point | Decomposes before boiling |
| Synonyms | 2,5-Dibromo-1,4-benzenedicarboxylic acid |
| Smiles | C1=C(C(=CC(=C1C(=O)O)Br)C(=O)O)Br |
| Inchikey | ZXGAQSGGZVEFEP-UHFFFAOYSA-N |
| Storage Temperature | Room temperature, dry and well-ventilated area |
As an accredited 2,5-Dibromoterephthalic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 2,5-Dibromoterephthalic Acid is supplied in a sealed, amber glass bottle, 25 grams, labeled with hazard information and batch details. |
| Shipping | 2,5-Dibromoterephthalic Acid is shipped in tightly sealed containers, protected from moisture and direct sunlight. It should be handled according to standard hazardous material regulations, with appropriate labeling. Shipping is typically performed by certified carriers to ensure compliance with chemical safety and transportation guidelines, minimizing the risk of spills or contamination. |
| Storage | 2,5-Dibromoterephthalic acid should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from incompatible substances such as strong bases and oxidizing agents. Protect the chemical from moisture and direct sunlight. Properly label the storage container and ensure it is kept away from heat sources and ignition points to maintain stability and safety. |
Applications of 2,5-Dibromoterephthalic Acid in Industrial Manufacturing2,5-Dibromoterephthalic Acid serves as a key intermediate for several high-value industrial sectors. As a direct producer, we support downstream manufacturers by delivering consistent quality, traceability, and technical data for process integration in controlled industrial environments. 1. High-Performance Polyesters for Specialty FilmsManufacturers of specialty polyester films use 2,5-dibromoterephthalic acid as a co-monomer to impart flame retardancy and thermal stability. The acid is introduced during the esterification stage, reacting with glycols under controlled temperature and pressure. The bromine moieties enable compliance with fire safety norms required in electrical insulation and protective packaging. Film producers adjust the ratio based on the targeted flame-retardant specification, balancing process viscosity and final mechanical strength through controlled dosing. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
2. Synthesis of Flame-Retardant Polyamide ResinsIn the engineering plastics sector, producers incorporate 2,5-dibromoterephthalic acid to modify polyamide chains for enhanced flame resistance. The material is introduced via polycondensation with diamines such as hexamethylenediamine. Integrated control of bromine content permits downstream formulators to meet FMVSS 302 and EN 45545 requirements without excessive halogen use. Accurate metering ensures polymer molecular weight and melt flow properties remain in target ranges for extrusion and molding. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
3. Advanced Liquid Crystal Polymer (LCP) FeedstockProducers of liquid crystal polymers include this dibromo acid in their custom monomer mix to improve LCP processability and high-temperature behavior. The compound is reacted with hydroxybenzoic acid or other suitable monomers through melt or solution polycondensation, creating rigid-rod structures with engineered bromine sites for high temperature and flame-resistant molded goods. Stringent materials traceability and batch analytics are required to comply with electronics sector quality requirements. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
4. Synthesis of Specialty Dyes and Pigment PrecursorsColorant manufacturers employ 2,5-dibromoterephthalic acid as a core aromatic scaffold for specialty dye and pigment intermediates. This compound can undergo further halogenation, sulfonation, or amidation, serving as a starting point for brominated colorants used commercially in plastics, fibers, and functional inks. Strict handling protocols and documentation support full supply chain transparency for safety and regulatory inspection. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
5. Pharmaceutical Intermediate Production (Not for Direct API Use)Certain pharmaceutical intermediate manufacturers source 2,5-dibromoterephthalic acid for the preparation of complex heteroaromatic scaffolds. This acid supports Grignard, Suzuki, and direct amination reactions to yield precursors for imaging agents, diagnostic dyes, and research compounds. All handling, batch validation, and quality systems operate under cGMP where required for intermediary synthesis, with traceability through all production stages. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
|
Competitive 2,5-Dibromoterephthalic Acid 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
Flexible payment, competitive price, premium service - Inquire now!
After years of real-world production experience, we've honed our process for manufacturing 2,5-Dibromoterephthalic Acid, a specialty intermediate appreciated by both research and industry. This compound, with the formula C8H4Br2O4, carries twin bromine atoms at the 2 and 5 positions on a terephthalic acid backbone. Small structural differences like these—compared with unsubstituted or singly brominated analogues—unlock unique pathways for downstream synthesis. Often called a “building block” in the lab, this chemical takes on much broader significance during industrial scale-up.
We produce 2,5-Dibromoterephthalic Acid with a close eye on lot-to-lot repeatability. In practice, that means we never take shortcuts with purification, crystallization, or analysis. Many manufacturers use generic processes that result in batches carrying variable levels of mono- or tri-brominated byproducts. Even traces of these can sabotage advanced applications, like synthesis of specialty polymers or design of complex organic frameworks. Years of working side by side with end users convinced us that better control at source leads to smoother outcomes all the way down the supply chain.
We focus on achievable, not theoretical, purity grades. Our 2,5-Dibromoterephthalic Acid typically falls above 99% by HPLC, with strict specification on chloride and other halides. The product forms a fine, white to off-white crystalline powder, with moisture kept well under 0.5%. These targets aren’t just lab curiosities—they reflect direct feedback from industrial chemists who have battled inconsistent quality from brokers and secondary suppliers. Controlling for trace metals can be especially critical in catalytic settings; our own process limits iron, copper, and nickel residues to below 10 ppm each, because we have seen real-world performance failures when those limits aren’t met.
In contrast, off-the-shelf variants sourced via trading companies frequently blur the line between 2,5- and 2,6-isomers, or include significant terephthalic acid carryover. We’ve built in two levels of isomeric separation by recrystallization and column chromatography, which stem directly from process complaints shared by academic and pharmaceutical chemists. To this day, we track these minor impurities batch by batch, and we have set in place a routine for random third-party laboratory inspection. The driving force isn’t just compliance—it’s the reputation we earn from reproducible results in our customer’s hands.
Chemical synthesis at scale calls for flexibility and reliability. The two bromine atoms on this molecule aren’t arbitrary decoration—they serve as highly reactive handles for further transformation. In real manufacturing settings, this means 2,5-Dibromoterephthalic Acid provides a path into di-substituted aromatic systems without multiple protection and deprotection steps. That efficiency translates into fewer process steps, better atom economy, and reduced hazardous waste. Research groups at several prominent universities have shown that the molecule slots neatly into cross-coupling procedures, especially Suzuki and Sonogashira reactions, with high conversion and minimal side product formation.
We’ve seen increased use in specialty polymers, especially fire-retardant polyesters and advanced engineering plastics. Electronic component makers appreciate the ability to tailor dielectric constants by modifying the aromatic core with reliable halogen substitution. In medicinal chemistry, the tightly controlled bromine placement streamlines synthesis of candidate drug compounds for screening. Over the past decade, our technical support team has worked hands-on with R&D chemists in all these fields. In many collaborations, the transition from small-scale flask reactions to plant-scale kilns only succeeded after we solved subtle issues tied to moisture and trace inorganic residues.
Sorting through catalogs and online offerings, one could easily mistake similar dibrominated phthalic acids for interchangeable reagents. Direct experience, though, shows otherwise. Other halogenation patterns—like 2,3- or 2,6-dibromo—isomers—exhibit distinct electronic effects, which shows up as altered reactivity in cross-coupling or esterification steps. Our synthesis pathway, refined through repeated at-scale campaigns, locks in the 2,5 pattern. We’ve learned to dial in bromination conditions so as to minimize overreaction, which not only keeps costs stable but also allows for consistent downstream processing.
Price-driven sourcing from trading houses tends to overlook these subtle distinctions. Material that passes a basic melting point test may still carry significant organic impurities or a mixture of regioisomers. These can poison catalysts or complicate crystallization in later steps. By controlling the upstream chlorination and dibromination stages, we avoid most of the common selectivity traps. Our technical sales and R&D teams spend as much time talking process troubleshooting with end users as they do on the sales side. Every time a customer shares a case of process stoppage or unexpected reactivity, we have the background and batch records ready for root cause analysis. In tough regulatory climates, traceability beats the lowest-cost option every time.
Years ago, we made the mistake of releasing a batch with only basic HPLC screening and rough melting point analysis. End users in high-throughput screening ran into unexpected discoloration during product workups. Further analysis identified persistent traces of unreacted mono-bromo impurities and metal catalysts. We retrofitted our process, bringing in both GC-MS and ICP-MS analysis for every production batch. Today, researchers and plant engineers demand these data as routine QA—because the actual downstream cost of one bad lot can dwarf any short-term savings on raw materials.
Handling and packaging also merit attention. As a manufacturer, we fill every order in heavy-duty, moisture-proof containers. Even brief exposure during warehouse transfers can introduce enough moisture to affect stability. We found, after extensive customer feedback, that custom packaging improved shelf life, reduced caking, and minimized handling complications. Our technical support line spends many hours per month troubleshooting these logistics concerns with field engineers—not just filling orders with no context.
Sourcing specialty intermediates doesn’t end with purchase orders. Often, researchers and process engineers run into issues scaling from grams to kilograms or making small formulation tweaks. Our technical specialists routinely consult on these transitions. In one case, a customer’s continuous flow reactor encountered blockages traced back to micron-scale particulate from another supplier’s off-spec material—which contained non-crystalline amorphous content that misbehaved under heat. Our production setup, using staged recrystallization, avoided this issue and restored production yields.
Direct conversations yielded other improvements. Early on, a pharmaceutical partner needed guidance on using 2,5-Dibromoterephthalic Acid in palladium-catalyzed coupling at low ppm Pd loading. After experimenting with several purification options, they achieved clean conversion only after switching to our low-metals lot. In our experience, close support during process troubleshooting helps lock in both technical results and long-term relationships. Tight control at our end supports innovation at theirs, which leads to actual breakthroughs, not just efficient transactions.
Actual production conditions have changed dramatically under the latest environmental and end-use regulations. We see documentation requests expanding every quarter, especially in pharma and electronics manufacturing. Instead of treating paperwork as a burden, we’ve integrated batch-level traceability into day-to-day plant operations. Fully mapped origin data, signed COAs, and real impurity profiles are routine for us, because our partners need these for regulatory filings and final manufacture declarations.
We do not substitute specifications or cut corners to fill short-term orders. In disciplines like electronics, where even low-halide contamination can short out submicron circuitry, quality and documentation are non-negotiable. If an impurity or process aid cannot be fully documented, we rerun the lot or reject it outright. This zero-compromise attitude costs more up front, but saves weeks or months compared to inline revalidation or customer-side troubleshooting. With increased demand for environmental accountability, third-party audits have become part of normal business for us. These checks help us refine process control and showcase traceability without drawing lines at the shipping dock.
We see the main value of 2,5-Dibromoterephthalic Acid growing as research and industry stretch the definition of advanced materials. For example, new methods in covalent organic frameworks (COFs) and metal-organic frameworks (MOFs) take advantage of the regularity and reactivity offered by this molecule’s dual bromine substituents. Photonics groups experiment with it for tailoring absorption properties of complex organic semiconductors. Each application brings back a new set of process demands—from stricter phase purity for polymers, to lighter color profiles for visible light applications.
As feedback loops between our lab team and our customers shorten, we continuously dial in the synthetic process. Regular process reviews and audits have uncovered previously overlooked issues around bromination selectivity under specific temperature profiles. By documenting these details and cross-sharing solutions with industry partners, we foster continual progress. Every unforeseen impurity profile, every batch variation, translates into notes and process tweaks that impact subsequent manufacturing campaigns.
Having built and run the same production lines for years, we know exactly where the bottlenecks and pain points arise. Analytical chemists on our team interface with customers not just at the tail end of QC, but during experiment design and troubleshooting. Direct control over process conditions—from reagent quality to vessel cleaning protocols—enables us to stand by every batch that leaves our facility. We’ve watched resellers and third parties stumble over questions about origin, stability, or impurity content. For us, hands-on answering of these questions is just part of the job.
Internally, our process improvement cycles prioritize actionable data over abstract metrics. When a reactor upset or an unusual impurity pattern crops up, the team sits down and reconstructs every step—not to shield blame, but to root out the source and prevent recurrence. Knowledge built this way is practical, shareable, and not locked behind management or procurement. As the main manufacturer, our advantage comes from being accountable for everything from raw material intake to drum loading for final shipment.
Raw material markets and regulatory requirements continue to shift. Increased focus on brominated compound lifecycle and end-of-life management is already visible in some end-user markets. We have responded by probing new methods to recover and recycle process byproducts and solvents, investing in closed-loop treatment wherever possible. Tests with green chemistry alternatives to traditional bromination show promise, especially in reducing overall process waste. Technical partners often visit our plant to observe these improvements firsthand and provide feedback, which we incorporate into upcoming runs.
We remain alert to changing safety protocols and workplace exposures. Regular reviews and staff training keep our operation compliant and safe. In the rare case of a batch deviation or technical complaint, our in-house teams do not delay—engineers and chemists actively engage with affected customers, draw on established relationships, and arrange reprocessing or replacement shipments as required.
Global supply chains and local regulations demand responsiveness and flexibility. As the direct originator, we can answer questions about production conditions, leftover solvent residues, and detailed impurity spectra on short notice. This flexibility is only possible through real, hands-on facility management, not just distribution. When a new regulation or customer requirement surfaces, our on-site lab and process teams discuss how to test for new impurities or validate alternative synthetic routes. This boots-on-the-ground capability ensures we deliver more than just specification sheets—tangible support and transparent communication define our way of working.
2,5-Dibromoterephthalic Acid serves as more than just a chemical name or catalog entry to us. Each kilogram represents practical experience, repeated feedback, and hard-won process knowledge. Decades spent refining synthesis, handling, purification, and documentation have convinced us that direct manufacturing involvement produces quality that traders and resellers cannot replicate. Whether destined for high-throughput research or commercial-scale industrial reactors, the product carries a pedigree that stands up to scrutiny in the field. For customers who need more than just commodity molecules, our reputation is built on persistence, transparency, and respect for demanding technical needs.