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4,5-Dibromo-2-Furaldehyde

    • Product Name 4,5-Dibromo-2-Furaldehyde
    • Alias 4,5-Dibromo-2-furaldehyde
    • Einecs 225-047-6
    • 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
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    Specifications

    HS Code

    738853

    Chemical Name 4,5-Dibromo-2-Furaldehyde
    Cas Number 31121-39-8
    Molecular Formula C5H2Br2O2
    Molecular Weight 265.88 g/mol
    Appearance Light yellow to orange crystalline solid
    Melting Point 96-99 °C
    Density 2.31 g/cm³ (approximate)
    Solubility Slightly soluble in water; soluble in organic solvents
    Purity Typically ≥97%
    Smiles C1=C(C(=O)C=O)C(=O)OC1BrBr
    Inchi InChI=1S/C5H2Br2O2/c6-3-1-4(7)9-5(8)2-3/h1-2H

    As an accredited 4,5-Dibromo-2-Furaldehyde factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing A 25g amber glass bottle with tamper-evident cap, clearly labeled "4,5-Dibromo-2-Furaldehyde," hazard symbols, and chemical details.
    Shipping 4,5-Dibromo-2-Furaldehyde is shipped in tightly sealed containers, compliant with chemical safety regulations. The package must be labeled as hazardous, protected from light, moisture, and incompatible substances. It should be handled by trained personnel, with documentation including the Safety Data Sheet (SDS) provided, ensuring safe and regulatory-compliant transportation.
    Storage 4,5-Dibromo-2-Furaldehyde should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from direct sunlight and incompatible materials such as strong oxidizing agents. Store it at room temperature and avoid exposure to moisture. Label the container clearly and restrict access to trained personnel to ensure safe handling and minimize risk of contamination or degradation.
    Application of 4,5-Dibromo-2-Furaldehyde

    Applications of 4,5-Dibromo-2-Furaldehyde in Industrial Manufacturing

    As the original manufacturer, we support global industrial partners by supplying 4,5-Dibromo-2-Furaldehyde for use in advanced chemical synthesis. Below, we outline verified, targeted industrial scenarios where this intermediate is essential, detailing regulatory compliance, practical formulation ranges, integration into downstream processes, and typical final product categories.

    1. Pharmaceutical Active Intermediate Manufacturing

    4,5-Dibromo-2-Furaldehyde serves as an indispensable building block in complex heterocyclic API synthesis, including new generation anti-infective and anti-cancer candidates. Pharmaceutical companies incorporate it into advanced multi-step routes requiring precise halogenated intermediates to ensure high yield and impurity control in subsequent reaction sequences. The material enters downstream at the key ring-forming or bromination stage, directly impacting both potency and traceability of the active substance.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for APIs
    • USP General Chapter <797>
    • EU GMP Part II
    • Chinese Pharmacopoeia (for domestic production)

    Typical usage ratio

    • 0.8%–2.5% w/w per batch, relative to total intermediate mass, adjusted based on stoichiometry of target molecule and yield optimization during scale-up

    Downstream process integration

    • Introduced at the heterocycle formation, acylation, or halogen exchange step; handled in closed reactors to ensure controlled addition for high batch reproducibility

    Final product types

    • Oncology drug intermediates
    • Anti-infective pharmaceutical APIs
    • Synthons for rare disease actives

    2. Agrochemical Synthesis (Herbicide and Fungicide Intermediates)

    The compound plays a critical role in the preparation of specialty intermediates for selective herbicides and fungicides. Its dual brominated furan structure enables precise substitution reactions that impart selectivity and activity to final crop protection agents. Agrochemical producers utilize the compound within tightly controlled batch processes for the installation of key functional groups necessary for field performance.

    Industry compliance standards

    • FAO/WHO Specifications and Guidelines for Agricultural Pesticides
    • ISO 9001:2015 Quality Management for Agro Inputs
    • EU Regulation (EC) No 1107/2009 on plant protection products
    • US EPA Registration guidelines for new technical grade active substances

    Typical usage ratio

    • 1.0%–3.5% by weight, depending on the desired bromination density and selectivity in the final molecular structure

    Downstream process integration

    • Added during the initial aromatic bromination or furaldehyde coupling reactions in pilot and commercial scale synthesis

    Final product types

    • Grass-selective herbicide intermediates
    • Systemic fungicide intermediates
    • Soil treatment agent synthons

    3. Specialty Dye & Optical Brightener Synthesis

    Manufacturers of high-performance dyes and optical brightener intermediates value this compound for constructing brominated furan backbones which impart intense chromophoric activity and tunable wavelength absorption. Its integration boosts the efficiency of functional dyes used in textiles and imaging, allowing downstream producers to achieve stringent purity and color strength requirements in the specialty colorant sector.

    Industry compliance standards

    • OEKO-TEX Standard 100 (for textile dyes)
    • REACH Regulation (EC No 1907/2006) Registration & Authorization
    • ISO 14001 Environmental Management for Colorant Production
    • ZDHC MRSL (Manufacturing Restricted Substances List)

    Typical usage ratio

    • 0.5%–1.7% as a color precursor or modifying agent, customized by reaction conditions and color depth requirements

    Downstream process integration

    • Charged at the chromophore assembly or bromination stage, using controlled addition methods to prevent over-bromination and ensure batch uniformity

    Final product types

    • High-durability textile dyes
    • Optical brightener intermediates
    • Triarylmethane dye building blocks

    4. Electronic Chemical Materials (Photoresist and OLED Intermediates)

    This specialty raw material is utilized by electronic chemical formulators synthesizing high-purity photoresist and organic light-emitting diode materials, where dual bromine and aldehyde functionality must be preserved for precision pattern transfer and emission optimization. Downstream, formulators depend on its consistent performance in key organic coupling and crosslinking steps, central to the quality and life-span of the final devices.

    Industry compliance standards

    • IEC 62474 Material Declaration for Electronic Industry
    • RoHS Directive 2011/65/EU
    • JPCA-ES-01 Printed Circuit Board Material Standards
    • TSCA Inventory Listing (for US domestic manufacture or import)

    Typical usage ratio

    • 0.2%–1.1% in pre-polymer or monomer synthesis, adjusted according to required photo-reactivity and emission wavelength

    Downstream process integration

    • Introduced in coupling or crosslinking stages for oligomeric or monomeric precursors, handled within high-cleanliness environments to maintain electronics-grade purity

    Final product types

    • Photoresist resin intermediates
    • OLED blue and green light emitters
    • Specialty organic semiconductors

    5. Advanced Polymer Modifier Synthesis

    Producers of performance polymers and specialty resins use this intermediate for the targeted functionalization of polymer backbones, enhancing flame retardancy, chemical resistance, and mechanical stability. The dual bromine groups facilitate covalent integration during controlled radical grafting or extension reactions, allowing formulators to introduce specific reactive sites for downstream crosslinking or compatibility tuning.

    Industry compliance standards

    • UL 94 Flammability Standard (for flame-retardant plastics)
    • ASTM D638 (for resin tensile properties)
    • ISO 9001:2015 Quality Management Systems (for polymer production)
    • REACH SVHC List compliance

    Typical usage ratio

    • 0.3%–1.0% by weight, set based on desired modification level and compatibility with base polymer matrix

    Downstream process integration

    • Added during the modifier synthesis or direct melt blending for functional group introduction, typically in twin-screw extrusion or batch reactor setups

    Final product types

    • Fire-resistant engineering plastics
    • Specialty adhesive resins
    • Reactive oligomer additives for automotive components
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    Certification & Compliance
    More Introduction

    4,5-Dibromo-2-Furaldehyde: Precision in Halogenated Furan Chemistry

    A Closer Look at 4,5-Dibromo-2-Furaldehyde

    Moving halogens onto the furan nucleus often creates remarkable opportunities in fine organic synthesis and advanced materials, and 4,5-Dibromo-2-Furaldehyde stands out as a prime example. Over years of hands-on manufacturing at scale, our team has seen this compound become indispensable for research laboratories and industrial innovators alike. What makes it special isn’t just the bromine atoms at the 4 and 5 positions, but the reactivity those groups unlock when coupled with the reactive formyl at the 2-position.

    The appearance of 4,5-Dibromo-2-Furaldehyde—frequently described as a pale or light yellow crystalline solid—provides a visual indicator of purity. High purity isn’t just a box to check off. Keeping impurities low prevents unwanted side products during downstream reactions, so controlling every part of the process, from selecting raw furan to final purification, demands attention. Our batches meet specs routinely checked by both GC and HPLC, not because the market mandates it, but because downstream users rely on reproducibility day in and day out.

    Chemical Profile and Physical Characteristics

    The structure features bromine atoms that give the molecule unique electronic character. Solid at room temperature, 4,5-Dibromo-2-Furaldehyde dissolves well in many organic solvents including ethanol, dichloromethane, and ethyl acetate, all favorites among synthesis chemists. Certain solvents work better depending on the approach—a customer focused on coupling reactions often prefers dichloromethane for both solubility and ease of workup. Customers in polymer synthesis often choose solvents to match their monomers or processing equipment. We see requests for advice about solvent compatibility almost weekly, with customers reporting differing results depending on the cleanliness, water content, or temperature control of the solvent. That anecdotal feedback from real-world production lines informs how we sharpen our own purification and drying protocols.

    Melting point serves as a reliable check for both identity and lot-to-lot consistency. In our production facilities, melting point checks are standard for each batch. Consistency in this value signals reliable product with minimal byproduct contamination, which matters for those developing regulated pharmaceuticals or tight-tolerance electronic materials.

    Comparing 4,5-Dibromo-2-Furaldehyde with Similar Furan Halides

    Customers regularly weigh the advantages of 4,5-Dibromo-2-Furaldehyde against related compounds—this includes mono-brominated furaldehydes or multi-brominated furans without an aldehyde function. Each variant opens different doors in chemistry. The dibromo configuration places bromines adjacent on the ring, which amplifies the compound’s electrophilicity. This proves crucial for selective cross-coupling reactions and for quickly building complexity onto furans. Mono-brominated versions tend to react more slowly and often force the chemist to use harsher conditions or accept a lower yield.

    Aldehyde functionalization at the 2-position offers a direct launching point for a range of condensation, cyclization, and addition strategies. Chemists creating pharmaceutical scaffolds or advanced conjugated polymers prefer the dibromo-aldehyde because it spares them the challenge of difficult halogenation on sensitive intermediates. Clients from universities to multinational R&D teams report that the ease of manipulating both functional partners on a single robust molecule saves them weeks of development time.

    Other halogenated furaldehydes, for instance those bearing chlorine or iodine, differ in reactivity and environmental profile. Iodinated analogues, while occasionally more reactive, become prohibitively expensive and hard to store on the shelf due to their instability and sensitivity to light and heat. Chlorinated versions, on the other hand, often require entirely different reaction conditions and give lower selectivity in many cases. Years of feedback confirm that bromines strike a sweet spot: stable enough to ship and store, reactive enough to function as versatile synthons.

    Typical Uses and Customer Feedback

    Pharmaceutical discovery leads the pack in terms of application volume. Project teams synthesizing novel heterocyclic libraries, enzyme inhibitors, or oncology drug candidates leverage the dibromo pattern for selective couplings, Suzuki, Stille, or Buchwald-Hartwig reactions. Beyond drug discovery, several customers in materials science report benefits for creating advanced functional polymers. They design monomers with both electron-withdrawing and electron-donating components to tailor conductivity or photophysical properties. 4,5-Dibromo-2-Furaldehyde’s clean, high-yielding reactions mean less purification downstream—something R&D chemists and scale-up process engineers mention as a key productivity booster.

    Flavor and fragrance developers also use this molecule to construct complex aroma compounds related to furanones and other volatile aldehydes. Here, the stability during synthesis and versatility in transformations allow rapid iteration of new compound families. In university research, grad students trying to build exotic polyheterocycle libraries have found the compound’s reactivity enables synthesis projects on a manageable timeline, rather than dragging on for months.

    Observed Challenges and Solutions in Manufacturing

    Scaling up production doesn’t only mean multiplying batch size. It reveals every small flaw in process design, material sourcing, and quality control. Getting the desired dibromo aldehyde with high purity and yield takes careful control. Substitution at both the 4 and 5 positions can lead to side products if temperature or halogen source stoichiometry drifts. In earlier years, we saw run-to-run variation until we dialed in cooling rates during bromination. Feedback from contract synthesis partners helped guide improvements for minimizing overbromination—particularly under conditions that would otherwise generate tribrominated impurities.

    Handling large quantities needs experienced operators because bromine reagents pack environmental and health risks. Investing in advanced fume extraction and continuous monitoring has reduced both worker exposure and environmental release. Chemists on the floor rely on robust training protocols and protective equipment, all backed by documented incident rates and near-miss reviews. The importance of safe handling grows in step with mounting regulations. We adapted solvent recovery and waste neutralization systems to cut down on hazardous waste streams—something regulators, certification bodies, and our own internal benchmarks insist upon.

    Stability during storage and shipment is another concern we’ve addressed through choice of packaging and desiccants. Improperly sealed packages can let in moisture, which leads to hydrolysis or slow oxidation. Early on, we switched from fiberboard to inert-lined containers, then began batch-testing stored samples every few months so users never face degraded material. Reports from export customers reinforce that even long transoceanic shipments now deliver the same product quality as material pulled straight from our shelves.

    Customer Experiences: The Value of Consistency and Responsiveness

    Strong relationships with users inform how we prioritize improvements—researchers and scale-up teams are quick to flag any new impurity or shift in melting point. After shifting to a new bromine supplier to stabilize costs, spikes in trace byproducts briefly appeared. Rather than denying the issue, we reached out to every affected customer, supplied replacement lots, and switched the raw material back, before optimizing new purification steps to prevent recurrence. That direct feedback loop between synthesis chemists, quality control analysts, and our own technical team continues to shape production today.

    For customers in regulated industries, every batch of 4,5-Dibromo-2-Furaldehyde we ship includes documentation on trace metals, halogen residuals, and solvent residues. Not long ago, a pharmaceutical group flagged an uptick in one minor peak in their downstream analytics. We traced it to a subtle seasonal change in the ambient humidity affecting the crystallization stage. After installing a controlled-drying zone and recalibrating climate controls, subsequent tests proved the fix worked. This translates into reliable downstream results for synthesis teams, who count on our documentation and sample retention as part of their QA programs.

    We’ve partnered with specialty chemical buyers who run custom processes where every minor impurity profile could influence performance. Sharing detailed chromatograms—beyond certificate requirements—has helped them achieve faster regulatory clearance and sharper reproducibility data for their own clients. The chemistry community values such transparency, especially for high-value or high-sensitivity applications.

    Impact on Downstream Chemistry and Modern Synthetic Pathways

    4,5-Dibromo-2-Furaldehyde unlocks strategic paths in synthetic chemistry. By presenting two halogen handles in proximity, it offers efficient entry points for sequential or tandem couplings. Modern cross-coupling methods—whether using traditional palladium catalysis or state-of-the-art photoredox and nickel approaches—count on reliable feedstocks to avoid troubleshooting unpredictable reactivity. Reliable feedstock translates into faster timelines, cleaner products, and less rework for researchers. At scale, these savings accumulate dramatically.

    Multi-functionality in one molecule cuts reagent costs, reduces reaction steps, and streamlines purification. Polymer scientists favor the dibromo pattern for preparing furan-based backbones with regular halogen points, which drives uniform polymerization and sharpens properties such as conductivity and processability. Universities submit requests for bulk material at predictable intervals corresponding to funding cycles—offering bulk packaging and verified stability helps them plan multi-step syntheses during busy academic years.

    We’ve watched our product enable synthetic access to otherwise hard-to-make fused heterocycles, multi-dentate ligands, and complex building blocks for sensors and optoelectronics. By combining utility, stability, and accessibility on a consistent basis, the compound supports the forward march of discovery.

    Lessons Learned from Direct Industry Engagement

    Early users sometimes found scale-up tricky. We fielded calls about sluggish reactions or polychloro byproduct formation when other suppliers’ batches were involved. Our in-house chemists regularly troubleshoot side-by-side with forward-thinking customers, reviewing data, analyzing impurity profiles, or even sending technical specialists overseas to troubleshoot tricky process bottlenecks. Universal lessons emerge from these exchanges—the source and purity of each reactant influence outcomes more than theory alone might suggest. It’s the hands-on team, watching the distillation and drying cycle, that often spots the fix before it ever shows up in a formal analytical report.

    Hazards from rough handling, transport delays, or package breaches during customs clearance can jeopardize an entire project. That knowledge pushed us to reinforce our packaging and add tamper-evidence seals. We report frequent updates to our export partners and stand ready to retrieve and analyze suspect samples—a direct outcome of field complaints from the past.

    Addressing legacy environmental concerns led to installing solvent capture and recycling lines in our synthesis departments, and to carefully screen effluent streams for persistent brominated byproducts. Balancing customer need with sustainable practices has led to measurable reductions in waste profile year over year.

    Regulatory Focus and Ongoing Quality Assurance

    Regulatory expectations in chemical manufacturing only grow tighter. Customers—especially those in pharmaceuticals and advanced electronics—must document every possible trace impurity. In response, our analytics team constantly revises detection limits and collaborates with customers on the newest analytic techniques, from ultra-trace GC-MS to ion chromatography. Routine process reviews and audits support lot traceability from starting material to packaged product. That diligence isn’t just about compliance; it keeps us flexible as new statutory frameworks appear, particularly in key export markets.

    Our engagement with independent third-party auditors, both local and from international certification bodies, validates not only product quality but also safety and environmental controls onsite. Documentation for each lot covers origin, processing, storage, and full analytic details—often exceeding regulatory requirements—to give research, QA, and production teams exactly the data they need.

    Annual process reviews now incorporate direct voice-of-customer reporting. Users who raise even minor out-of-spec events find their issues captured into risk management protocols, not treated as outliers. Inclusion of external audit and customer feedback in root cause analysis has led to tangible improvements such as modified drying processes, redesigned containment, and upgraded purification steps.

    Future Steps and Areas for Innovation

    Continued demand from diverse sectors drives us to improve yield, reduce waste, and develop new forms—whether that means higher-purity grades or solvent-free crystalline forms for customers with unique regulatory or practical concerns. Environmental trends and customer requests push R&D to test less toxic halogen sources and explore new routes for the core dibromo aldehyde. Any new synthetic protocol adopted must scale seamlessly, avoid new hazards, and fit neatly into existing customer workflows.

    We’re also collaborating with academic and industry partners to explore bio-based sources of furan precursors and recyclable bromination agents. Modern chemistry trends toward green, safer, and cleaner processes, and these imperatives guide both investment and hands-on process improvement internally. Partner feedback continues to define new applications: from smarter battery materials to biomedical scaffolds.

    Conclusion: Trusted Partner for Halogenated Furans

    Longstanding relationships with demanding customers have shaped how we make and deliver 4,5-Dibromo-2-Furaldehyde. Our direct experience as a manufacturer has shown that attention to detail—process, analytics, packaging, and customer interaction—drives consistent outcomes and tangible benefits for every user, whether in the lab, in the pilot plant, or out in full industrial synthesis. Each improvement, born of customer interaction and field report, becomes part of the product’s story and performance. Our focus on reproducibility, safety, and responsiveness helps researchers in drug discovery, advanced materials, and specialty chemicals keep moving forward, confident that their feedstocks will behave by the book and save them hours of troubleshooting and cleanup.