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2,3-Dibromofuran-5-Carboxylic Acid

    • Product Name 2,3-Dibromofuran-5-Carboxylic Acid
    • Alias 2,3-Dibromo-5-furoic acid
    • Einecs 809-024-8
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry sales7@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    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 & Storage
    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.
    Application of 2,3-Dibromofuran-5-Carboxylic Acid

    Applications of 2,3-Dibromofuran-5-Carboxylic Acid in Industrial Manufacturing

    2,3-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) Synthesis

    This 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

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • US Pharmacopeia (USP) General Chapter 1086
    • European Pharmacopoeia (Ph. Eur.) Section 2.4
    • FDA DMF Typing Systems for API Intermediates

    Typical usage ratio

    • 0.2–0.8 molar equivalent per API target, with stoichiometry adjusted following route optimization studies and based on impurity profiles in pilot runs

    Downstream process integration

    • Reagent charged after initial coupling or cyclization steps; enters directly before key halogenation stage of multi-step organic synthesis; followed by solvent extraction and recrystallization in cleanroom controlled zones

    Final product types

    • Oncology targeted small molecule drugs
    • Innovator and generic API batches
    • Intermediates for anti-inflammatory therapeutics
    • Advanced research compounds for clinical trial supply

    2. Crop Protection Active Ingredient Manufacturing

    Manufacturers 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

    • FAO/WHO Joint Meeting on Pesticide Specifications (JMPS)
    • OECD Guidance Document 23 on Residues in Crops
    • ISO 9001:2015 for Crop Protection Initial Synthesis
    • China GB/T 1603-2020 Pesticide Active Ingredient Quality Standard

    Typical usage ratio

    • 0.15–0.45 wt% per synthetic batch of target active, fine-tuned based on required bromination depth and monitored by HPLC residuals QC

    Downstream process integration

    • Dosed in stepwise reactions after initial ring formation; followed by halogen exchange, purification column loading, and compatibility checks within pilot greenhouse simulation studies

    Final product types

    • Bromofuran-based fungicides
    • Insecticidal actives for seed treatment
    • Agrochemical intermediates for formulation R&D
    • Crop protection reference standards

    3. Fluoropharmaceutical Intermediate Development

    Specialty 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

    • cGMP for Radiopharmaceuticals (USP General Chapter 825)
    • EU Good Manufacturing Practice Annex 3 for Radiopharmaceuticals
    • U.S. NRC Regulatory Guide 10.8, Revision 3 (Radiopharmaceuticals)
    • ICH Q9 (Quality Risk Management)

    Typical usage ratio

    • 0.05–0.20 molar ratio per labeled molecule, titrated according to isotope exchange efficiency and tracer batch scale

    Downstream process integration

    • Receives direct input at the isotope exchange or halogenation module after primary backbone construction; radiochemical yields validated by in-line mass spectrometry and HPLC

    Final product types

    • Radiolabeled diagnostic agents
    • Fluorinated PET scan precursors
    • Research radiotracers
    • Preclinical imaging intermediates

    4. High-Performance Polymer Additive Synthesis

    Advanced 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

    • UL 94 Standard for Safety of Flammability of Plastic Materials
    • ASTM D2863 Oxygen Index Test
    • RoHS Directive (2011/65/EU) for Restricted Substances
    • ISO 9001:2015 for Quality Management Systems

    Typical usage ratio

    • 0.05–0.25% by weight in total polymer resin, with variation guided by flammability testing and mechanical performance against specification benchmarks

    Downstream process integration

    • Introduced at compounding before extrusion or injection molding; homogeneity monitored during melt processing; post-curing properties checked in finished article testing

    Final product types

    • Flame-retardant electronic housings
    • Specialty cable insulation compounds
    • Polymeric encapsulants for advanced electronics
    • Architectural and transit composite materials
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    Certification & Compliance
    More Introduction

    2,3-Dibromofuran-5-Carboxylic Acid: A Key Intermediary for Precision Synthesis

    Bringing Advanced Intermediates to Real-World Chemistry

    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.

    The Heart of Halogenated Furan Chemistry

    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.

    The Challenge of Controlled Halogenation

    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, Storage, and Real-World Use

    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.

    Where 2,3-Dibromofuran-5-Carboxylic Acid Outpaces Similar Intermediates

    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.

    Model, Specifications, and Real Output Versus Data Sheet Promises

    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.

    Industrial Uses, from Laboratory to Production

    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.

    Why Consistency in Manufacturing Matters

    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.

    Supporting Innovation in Research and Industry

    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.

    Environmental Responsibility and Worker Safety

    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.

    Challenges Facing the Market Today

    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.

    Continuous Improvement through Direct Feedback

    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.

    Conclusion: The Value of Reliable Chemistry

    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.