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HS Code |
522308 |
| Chemicalname | 2,3-Dibromofuran-5-Carboxylic Acid |
| Molecularformula | C5H2Br2O3 |
| Molecularweight | 285.88 g/mol |
| Casnumber | 82512-33-8 |
| Appearance | Off-white to light brown solid |
| Boilingpoint | Decomposes before boiling |
| Solubility | Slightly soluble in water; soluble in organic solvents |
| Purity | Typically >95% (dependent on supplier) |
| Smiles | C1=C(C(=O)O)C(Br)=C(Br)O1 |
| Inchi | InChI=1S/C5H2Br2O3/c6-2-1-3(5(8)9)10-4(7)11-2/h1H,(H,8,9) |
| Storageconditions | Store at 2-8°C, in a dry, well-ventilated place |
| Hscode | 2932190090 |
As an accredited 2,3-Dibromofuran-5-Carboxylic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The packaging is a 25-gram amber glass bottle, securely sealed, labeled with chemical name, hazard symbols, and handling instructions. |
| Shipping | 2,3-Dibromofuran-5-carboxylic acid is shipped in tightly sealed containers, protected from moisture and light. Packages comply with hazardous material regulations due to its corrosive and potentially harmful nature. Shipping is via certified carriers, with clear hazard labeling and accompanying safety documentation, ensuring safe and compliant handling during transit. |
| Storage | 2,3-Dibromofuran-5-Carboxylic Acid should be stored in a tightly sealed container, protected from light and moisture, in a cool, dry, and well-ventilated area. Keep away from incompatible substances such as strong oxidizers and bases. Ensure proper labeling and store at room temperature or as specified by the supplier. Use appropriate personal protective equipment when handling and storing. |
Applications of 2,3-Dibromofuran-5-Carboxylic Acid in Industrial Manufacturing2,3-Dibromofuran-5-carboxylic acid is a specialty intermediate used in high-value synthesis routes for pharmaceuticals, agrochemicals, and advanced materials. Our manufacturing control ensures tight specifications for integration across regulated and research-intensive sectors. Below, we outline core downstream applications with detailed process considerations and compliance guidance for each sector. 1. Active Pharmaceutical Ingredient (API) SynthesisThis intermediate finds its main use in complex API synthesis, particularly for heterocyclic compound production in oncology and anti-inflammatory drugs. Its chemical reactivity allows precise bromination steps not achievable with alternative feedstocks, and customers rely on the purity level maintained in our GMP environment to meet their regulatory submissions. During process scale-up, formulators adjust input molarities based on target molecule yield and impurity profile studies. Strict process controls manage product quality in final crystallization and purification phases, as required under global pharmacopoeia monographs. Industry compliance standards
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2. Crop Protection Active Ingredient ManufacturingManufacturers of next-generation crop protection actives use this raw material to introduce bromofuran units crucial for enhanced bioactivity against select insect or fungus species. Its controlled reactivity enables fine-tuned synthesis, meeting regulatory residue limits and downstream environmental fate requirements for commercially released formulations. Process engineers scale the usage according to the activity screens and agrochemical formulation registration needs, balancing cost and efficacy with compliance to jurisdictional standards. Industry compliance standards
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3. Fluoropharmaceutical Intermediate DevelopmentSpecialty fluoropharmaceutical companies use 2,3-dibromofuran-5-carboxylic acid in the creation of radiolabeled and fluorinated species. Its molecular structure supports regioselective halogen exchange, a key step that dictates radiochemical purity and patient safety. Operators monitor handling under radiation safety protocols and maintain compliance with documentation required for clinical compound supply. Input ratios depend on isotope exchange yields and specific activity calibration during labeled drug candidate synthesis. Industry compliance standards
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4. High-Performance Polymer Additive SynthesisAdvanced materials manufacturers use this chemical to introduce functionalized bromofuran moieties in specialty polymer backbones designed for flame retardant applications or electronic encapsulation. Strict material selection processes ensure adequate incorporation and thermal stability testing. Usage amount is determined via formulation trials designed to meet finished product standards for safety, fire rating, and electrical insulation. Integration occurs at the monomer or pre-polymer blending stage, with post-synthesis analysis via spectroscopy and mechanical evaluation. Industry compliance standards
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At our manufacturing facility, the drumbeat of specialized chemical production underscores our commitment to practical, reliable chemistry that fits industrial need. 2,3-Dibromofuran-5-Carboxylic Acid is a product born from technical persistence and an intimate understanding of reproducible synthesis. Our chemists, with hands-on experience in halogenation and furan chemistry, recognize the role of this compound as an important intermediate in the pursuit of advanced molecules. Years of scaling up bench-top findings to robust batch production, without compromising on analytic consistency, taught us the subtle differences between lab-grade synthesis and true industrial reproducibility.
2,3-Dibromofuran-5-Carboxylic Acid has quietly become a staple for methodical route development in modern synthetic chemistry. Its unique structure – a furan ring substituted specifically at the 2 and 3 positions with bromine, and a carboxylic acid group at the 5 position – allows for selective downstream modifications. This molecular arrangement doesn't just distinguish the compound. It opens doors for coupling reactions and complex building block integration, especially where selective halogenation patterns are indispensable.
Throughout scale-up, we've seen how purity and structural reliability impact yield downstream. In multi-step syntheses, subtle impurities or regioisomeric contamination often derail final outcomes. Trusting only in methodical, stepwise monitoring, our production teams maintain close oversight from raw material sourcing through crystallization and drying. We know that in the field, compromised materials can set entire projects back.
From experience, synthesizing 2,3-Dibromofuran-5-Carboxylic Acid demands a quality approach to bromination control. The chemistry is not simply about adding two bromines; it's about stopping at the correct position and avoiding overbromination, which produces undesired isomers and impure mixtures. We control temperature, solvent type, and reaction rate at every stage. Loss of control in these parameters quickly translates into inconsistent product and downstream inefficiencies.
Years on the production line brought a clear picture: halogenation byproducts rarely announce themselves until late-stage analytics. Only high-resolution NMR, HPLC, and mass spec can confirm the location of bromines and the carboxyl group. In-process adjustment, not guesswork, protects the function and fate of the molecule. That’s where years of practical experience separate reliable supply from batch-to-batch guessing.
Handling 2,3-Dibromofuran-5-Carboxylic Acid presents regular but manageable challenges. The compound typically presents as a solid, somewhat sensitive to moisture due to the polar nature of its acid group. Long experience in storage optimization taught us to focus on low-humidity conditions and proper sealing. During transfer or weighing, we rely on practical protocols to prevent caking or loss, as even modest moisture uptake can affect downstream handling.
Chemists purchasing direct from a manufacturer often contact us for insight on solvent compatibility and reactivity. We routinely offer advice based on our daily exposure: the compound dissolves well in chlorinated solvents and many polar aprotic solvents, remaining stable for extended periods under cool, dry, and inert atmosphere storage. These facts do not arise from paperwork but from constant batch QC, where even minor shifts in storage bleed into observed reactivity or solubility.
Attempts to sidestep the exact structure of this compound by using mono-brominated or unsubstituted furan analogs rarely succeed. Our most seasoned synthetic partners report far greater selectivity in cross-coupling, Suzuki, and other transition-metal-catalyzed processes when both bromines are present at the 2 and 3 positions. Single-halogen structures leave too many variables open; side reactions multiply, yields drop, and purification becomes painful.
Even compared to 2,5-dibromo or 3,4-dibromo variants, the difference is clear. Reactions proceed with less unpredictability, and downstream substitution patterns remain sharp, almost never contaminated with off-target regioisomers. From day-to-day work, the tangible difference lies in how efficiently catalyst loadings translate to core modifications and how reliably protecting groups maintain selectivity throughout lengthy syntheses.
We produce 2,3-Dibromofuran-5-Carboxylic Acid under a model that values hands-on verification over generic packaging claims. Targeted purity meets or exceeds 98% by HPLC and NMR, but actual product quality always involves more than a number. Particle size, residual solvent content, color, and ease of dissolution all matter from the day product ships to the day it hits your reactor. We do not chase minimum specs; we verify with every lot that our material performs as expected in test-batch scale reactions.
Through direct, long-term supply agreements, our chemists often hear back from users working on delicate pharmaceutical intermediates, high-value synthesis, or novel materials development. Those teams report how switching from generic, less-controlled sources to our supply means fewer filtration problems, fewer column runs, and less material lost to unpredictable side reactions. Internal validation — not just paperwork — drives every change and tweak to our process.
Demand for 2,3-Dibromofuran-5-Carboxylic Acid surged with the growth of complex heterocyclic synthesis. In manufacturing environments, the compound supports a backbone of applications. One of the main use cases remains as a coupling partner in metal-catalyzed cross-coupling, frequently involved in assembling novel heterocyclic structures for pharmaceutical R&D teams seeking new leads. Each batch we produce supports diverse research, from medicinal chemistry to polymer design, where selectivity and reliability matter most.
Practical users draw a clear distinction between our product and more widely produced but less specific intermediates. Switching to our 2,3-dibrominated furan derivative, teams routinely cut hours from their synthetic planning and waste management. Reactions that formerly produced hard-to-separate byproducts now yield cleaner products, thanks to consistent reagent profiles and reliable halogen placement. Downstream processing becomes less labor-intensive, improving overall process economy beyond the confines of pure reactant cost.
Working in chemical manufacturing day-in, day-out teaches how the real cost of an intermediate rarely boils down to the direct price per kilo. Consistent, reliable performance from a batch saves time, reduces experimental repeats, and lowers total cost in a process stream. For 2,3-Dibromofuran-5-Carboxylic Acid, we've seen clients in both research and large-scale operations who suffered schedule overruns or production halts with inconsistent materials from unverified sources.
Raw numbers never tell the whole story. Once, a customer’s process consistently failed on scale-up, owing to undetected tars and minor side-products inherent to unreliable sourcing. By tightening our crystallization and wash protocols, and running head-to-head test reactions, we moved this customer out of a cycle of production setbacks. Such outcomes reflect daily decision-making — monitoring, retaining reference samples, and refusing to release batches that don’t meet rigorous practical tests.
Chemical research moves rapidly. Customers regularly request volumes adjusted to suit shifting demands, from small pilot runs to multi-kg lots. Our real-world adaptability relies not only on technical infrastructure but also on feedback loops between our technical team and our partners. Whether serving a pharmaceutical R&D division, addressing needs in specialty monomer synthesis, or fueling analytical method development, we ensure the same product quality at every batch size.
One research team, for instance, chose our 2,3-dibromofuran compound because initial bench trials from another source gave sporadic, low-yield outcomes. They traced this back to lower isomeric purity. Direct dialogue with our process chemists helped them tune their step conditions, resulting in higher, reproducible yields and much reduced byproduct formation. Our manufacturing workflow does not focus solely on pushing tonnage but in enabling better chemistry.
Manufacturing halogenated intermediates comes with specific environmental and safety pressures. Our teams operate under strict protocols to handle, neutralize, and safely dispose of brominated byproducts and waste streams. Through investment in in-house treatment, and constant attention to solvent recovery, every production run reflects practical solutions to real risk, rather than check-the-box regulatory compliance.
On the floor, worker training targets daily, real-world issues: dust protection, glove integrity, correct fume hood practices, and emergency readiness. Over the years, this reality-based training produced an unmatched record of incident-free operation. These protocols do not stem from abstract safety documents, but from a track record of thousands of batches produced and years of zero environmental deviation.
Shifting global supply chains have complicated sourcing of high-value intermediates. Quality standards, economies of scale and regulatory environments change unexpectedly, leaving synthetic chemists with inconsistent batches, longer lead times, and difficult price fluctuations. We’ve faced periods where upstream raw material shortages have forced innovations in process optimization and in-house recovery to keep consistent product flowing.
Recent years have also brought tighter scrutiny over halogenated intermediates, especially in regulated applications like drug development. Our manufacturing teams monitor evolving guidelines in real-time, update documentation, and verify compliance — not by outsourcing compliance but by maintaining total process control. Analysts, not administrators, verify every regulatory and quality checkpoint.
No manufacturing process stays static for long. Real-world production lines generate unexpected issues, from changes in raw material quality to minor tweaks in analytical methodology. Teams that refuse feedback from synthetic chemists lose ground to competitors. At every scale, our process evolves based on batch data, fail-point reviews, and customer feedback. Internal review sessions translate direct lab and production experience into process tweaks.
In one instance, feedback about difficult filtration on a particularly large synthetic run led our staff to identify and alter a small but significant variable — the rate of acid addition when quenching. Tuning this step reduced fine suspension, eased downstream separation, and resulted in faster, cleaner product verification. Such improvements only occur through honest, hands-on partnership rather than transactional supply.
At its core, the production of 2,3-Dibromofuran-5-Carboxylic Acid serves as a lesson in the value of process discipline, technical expertise, and constant vigilance. In the face of daily practical challenges, this chemical continues to differentiate itself from lesser intermediates and general-purpose reagents by delivering value through precision, reproducibility, and trusted support. From managing raw materials, controlling halogenation, ensuring quality, and responding to both regulatory shifts and customer feedback, our focus remains locked on making chemistry work for the real world.
As every chemist and process manager knows, the reliability of an intermediate can make or break weeks of hard work. Our story with 2,3-Dibromofuran-5-Carboxylic Acid reflects years of daily adaptation, technical rigor and a continuous pursuit of dependable, high-quality chemical supply.