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2,5-Dibromofuran

    • Product Name 2,5-Dibromofuran
    • Alias 2,5-Dibromofuran
    • Einecs 217-776-9
    • 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

    881024

    Chemical Name 2,5-Dibromofuran
    Cas Number 41443-07-6
    Molecular Formula C4H2Br2O
    Molar Mass 237.87 g/mol
    Appearance Pale yellow to light brown solid
    Melting Point 45-47°C
    Boiling Point 64-66°C at 2 mmHg
    Density 2.256 g/cm³
    Solubility In Water Insoluble
    Refractive Index 1.607 (20°C)
    Smiles Brc1cc(Br)oc1
    Pubchem Cid 70649

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

    Packing & Storage
    Packing 2,5-Dibromofuran is packaged in a 25g amber glass bottle, sealed with a screw cap, featuring clear hazard and identification labels.
    Shipping 2,5-Dibromofuran is shipped in tightly sealed containers, protected from light and moisture. It should be handled as a hazardous material, compliant with relevant regulations, such as UN 2810 (toxic liquid, organic, n.o.s.). Appropriate labeling, documentation, and packaging are required to ensure safety during transit and storage.
    Storage 2,5-Dibromofuran should be stored in a cool, dry, and well-ventilated area, away from direct sunlight, heat sources, and incompatible materials such as strong oxidizers. Keep the container tightly closed and properly labeled. Store in a chemical-resistant container, preferably made of glass or compatible plastic, and use secondary containment to prevent spills or leaks. Follow appropriate safety and regulatory guidelines.
    Application of 2,5-Dibromofuran

    Applications of 2,5-Dibromofuran in Industrial Manufacturing

    As a manufacturer dedicated to specialty chemical synthesis, we understand the unique role that 2,5-Dibromofuran plays in advanced chemical sectors. Its distinct reactivity enables precise functionalization steps in complex molecule construction, particularly in the pharmaceutical, agrochemical, and specialty materials industries. The following application scenarios detail realistic industrial applications, compliant operational practices, and end-material characteristics based on actual market usage.

    1. Pharmaceutical API Intermediate Synthesis

    Major pharmaceutical manufacturers utilize 2,5-Dibromofuran as a key building block for constructing furan-based heterocyclic intermediates, a class frequently used in targeted APIs for antiviral, anticancer, and anti-inflammatory therapeutic agents. The double bromine substitution enables efficient cross-coupling or metalation in the early phases of multi-step synthesis, with integration governed by cGMP practices and stringent pharmacopeia compliance. Selection of usage ratios depends on the specific yield optimization during the lead structure assembly, with downstream processing involving Suzuki-Miyaura or similar cross-couplings to produce the core active ingredient.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP <797> Pharmaceutical Compounding Guidelines
    • European Pharmacopoeia Monographs for Heterocyclic Intermediates
    • 21 CFR Parts 210 & 211 for Drug Manufacturing

    Typical usage ratio

    • Usage commonly ranges from 0.5% – 3% w/w relative to batch size, with precise adjustment based on stoichiometry and target molecule complexity.

    Downstream process integration

    • Added during the initial bromination or coupling stages of heterocycle synthesis for key intermediates.
    • Introduced under controlled inert gas conditions, often in jacketed glass reactors at monitored temperatures.

    Final product types

    • API intermediates for antiviral drugs (e.g., favipiravir analogues)
    • Heterocyclic scaffolds for oncology small molecules
    • Advanced intermediates for anti-inflammatory pharmaceutical agents

    2. Agrochemical Active Ingredient Development

    Manufacturers in crop protection and agrochemical innovation employ 2,5-Dibromofuran in the preparation of active molecules for insecticides and fungicides, particularly those relying on furan ring frameworks with halogen substitutions. Downstream labs typically utilize this compound at the selective halogenation or ring-formation stages, where its electron-withdrawing character guides regioselective transformations. Quality assurance in this segment links directly to regulatory controls on agrochemical ingredients and batch consistency for field application safety.

    Industry compliance standards

    • FAO/WHO Specification for Pesticide Preparation (JMPS)
    • OECD Good Laboratory Practice (GLP) for Agrochemical Synthesis
    • ISO 9001:2015 for Quality Management in Chemical Manufacturing
    • REACH Registration (EC 1907/2006) for new agrochemical substances

    Typical usage ratio

    • Typically 1–4% of the reaction volume, modulated based on the target compound yield and reaction efficiency.

    Downstream process integration

    • Applied in the halogenation stage for intermediate formation during synthesis of novel crop protection agents.
    • Fed into stirred batch reactors equipped with in-line bromine scavenging purification modules.

    Final product types

    • Selective insecticide actives targeting resistant species
    • Systemic fungicide compounds for high-value crops
    • Seed coating agent intermediates

    3. Specialty Electronic Material Precursors

    Producers of organic electronic materials, such as those for OLED and OFET applications, include 2,5-Dibromofuran in the synthesis pipeline for advanced functional polymers. The brominated furan ring acts as a reactive site for Suzuki or Stille coupling, facilitating the construction of semiconducting oligomers and polymers. Strict material traceability, in compliance with international electronics and semiconductor standards, ensures consistent downstream integration and reliable device performance.

    Industry compliance standards

    • RoHS Directive (2011/65/EU) for hazardous substance restriction
    • IEC 61249-2-21 for halogen-free electronic materials
    • ISO 14001:2015 for environmental manufacturing management
    • IPC-4101B for base materials in printed electronic applications

    Typical usage ratio

    • For polymer precursors, 0.1–1.5 molar equivalents per monomer unit, with adjustment based on polymerization scale and target molecular weight.

    Downstream process integration

    • Feeds into monomer synthesis lines ahead of metal-catalyzed cross-coupling or lithiation steps.
    • Reacts in pilot-scale reactors under controlled temperature and atmosphere to limit side-products.

    Final product types

    • Emissive layer precursors for OLED displays
    • P-type and n-type semiconducting polymers for organic transistors
    • Material additives for printable solar cells

    4. Fine Chemical Custom Synthesis for Research

    Contract synthesis and research organizations require stable and reactive halogenated furans for novel molecule development in fine chemicals, dyes, and high-value reference compounds. In this environment, researchers exploit the defined positions of bromine atoms for unique substitution patterns. Applications involve tight adherence to laboratory chemical safety protocols, and batch documentation supports reproducible, publication-ready chemistry.

    Industry compliance standards

    • GLP (Good Laboratory Practice) OECD Principles (ENV/MC/CHEM)
    • Hazardous Chemicals Registration under local and regional regulations
    • ISO/IEC 17025 for testing and calibration laboratory standards
    • Responsible Care® program for process and employee safety

    Typical usage ratio

    • Generally used in stoichiometric quantities (1–1.2 equivalents) relative to substrate molecules in preparative-scale synthetic schemes.

    Downstream process integration

    • Utilized at the initial synthetic step in flow or batch mode, serving as a coupling partner or synthon for customized molecular architecture.
    • Process involves precise addition under argon, with monitored exothermic control for sensitive intermediates.

    Final product types

    • Research intermediates for structure–activity studies
    • Labeled compounds for analytical standards in mass spectrometry
    • Building blocks for custom dye synthesis and specialty fine chemicals
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    Competitive 2,5-Dibromofuran prices that fit your budget—flexible terms and customized quotes for every order.

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    Certification & Compliance
    More Introduction

    2,5-Dibromofuran: Shaping Synthesis with Precision and Purity

    Real Results in Advanced Chemistry

    2,5-Dibromofuran takes its place in our portfolio as a specialty building block that speaks to the standards of chemists looking for both reliability and flexibility. We’ve produced this compound for years, tailoring our own approach to match the technical demands that research and large-scale custom synthesis consistently require. There’s no shortcut here—every batch flows through rigorous quality checks, controlled crystallization, and targeted distillation. Not all furan derivatives respond alike to halogenation conditions, and our practical experience with furan chemistry helps us keep yields and purity high, supporting the advanced needs of agrochemical discovery, new pharmaceuticals, and high-value material innovation.

    Context and Color: What Sets 2,5-Dibromofuran Apart

    Anyone working with furan rings sees quickly how each modified compound finds its own job. Some prefer 2-bromofuran for mono-substitution; others reach for chlorinated, iodinated, or multi-substituted derivatives. We navigate the less forgiving parts of furan bromination, starting from stabilized feedstocks and controlling addition rates to capture the desired regioselectivity at the 2 and 5 carbons—no need to wrestle with isomeric mixtures or chase down purifications.

    Fresh technical documentation highlights how this dibrominated variant opens product development up where a single bromine just can’t. If you want two reliable points for coupling, 2,5-Dibromofuran matters. Conjugation strategies in medicinal chemistry often seize on the orthogonality of the 2,5-positions to build up frameworks for lead candidates. We watch customers replace both bromines in cross-coupling reactions, or strip one off selectively for stepwise diversification. Bromine atoms at these spots deliver highly reactive leaving groups for Suzuki, Stille, or Buchwald–Hartwig transformations.

    Consistency in Processing, Batch After Batch

    Our process control makes a difference. The product you receive today will echo the performance and specifications of last month’s and last year’s. We measure purity by GC and HPLC, confirming bromination exclusivity and managing traces of polybrominated byproducts. We have seen inconsistency from open-market sources wreck project timelines—impurities can tie up crucial catalysts, force extra purification, or even compromise structure confirmation. By maintaining our own furan ring sourcing, we clear away many variables that surprise less experienced producers. This helps keep hydrolysis-prone contaminants away from your sensitive reactions.

    Physical properties can’t be left to guesswork. We manage temperature and pressure during synthesis—boiling point and melting range match published values batch after batch. No two lots drift in color or solubility, because quality control catches instability before it escapes the production line. With 2,5-Dibromofuran, attention to the fine points of distillation and storage becomes more than just convenience. The decisions made at every stage—from starting material selection up to the packaging atmosphere—affect your ability to carry a molecule from test tube to production scale.

    Why Not Settle for Brevity in Choice?

    Customers sometimes ask why they shouldn’t just substitute an easier-to-obtain bromofuran or reach for mixed halogen derivatives. The answer: the specificity of 2,5-substitution avoids structural ambiguity. In practice, this keeps new compound libraries clean. For heterocyclic intermediates, broad isomer mixtures waste time and money—every extra peak on a chromatogram adds risk. We stick to direct bromination and isolation of the 2,5-isomer, refining every year based on feedback from medicinal and materials chemists who notice the difference. We don’t recommend random substitution or shifting to halogens with different leaving group reactivities unless there’s some strong justification in the reaction mechanism.

    The market offers a handful of bromofuran products. Mono-brominated forms—such as 2-bromofuran—limit diversity, and tri- or tetra-brominated versions lead to over-functionalized products that rarely fit the desired synthesis schemes. Our practical work has shown that the dibrominated, symmetrical nature of 2,5-Dibromofuran brings unique advantages for both convergent and divergent synthetic strategies. The molecular symmetry can be harnessed for constructing polycyclic frameworks, and in advanced agricultural chemistry, the ability to introduce two reactive centers saves several steps compared to sequential mono-bromination.

    Understanding the End-User Perspective

    We’ve shipped this compound to teams working at the edge of medicinal research, such as those targeting heterocycle-rich kinase inhibitors, to polymer chemists spinning new frameworks that demand accurate input on reactivity and stability. Many have shared their frustrations dealing with materials of inconsistent color, incomplete analysis, or lots packed under air that degrade before use. Brominated furans react with trace moisture; bodies familiar with the hazards of furanic aldehyde byproducts know how these can set back a campaign that relies on reliable sourcing. Our approach—handled in an inert atmosphere, sealed under nitrogen, and always certified by full trace documentation—keeps these headaches away.

    Price shopping sometimes tempts buyers toward attractive offers from middlemen or low-transparency resellers. The false savings rarely hold up after accounting for reprocessing, lost experiments, and time spent troubleshooting. We’ve traced the source of many “mystery peaks” in customer NMR spectra directly to imported, poorly characterized batches of dibromofuran. By continuing to focus on tight process discipline—right down to tamper-evident packaging—we deliver confidence along with every shipment.

    The Role of Specifications in Synthesis

    Full COA support means you see each batch’s water content, halide distribution, purity profile, and residue on evaporation. Beyond what’s written down, our chemists run spot-tests for applications like metal-catalyzed couplings, checking for background inhibition or irregular reactivity. The literature offers plenty of synthesis routes for 2,5-Dibromofuran, but putting these into consistent production stretches farther than graduate-level bench chemistry. By investing in glass lining, high-precision dosing equipment, and protected storage infrastructure, we keep the final compound faithful to the molecular structure you expect.

    Solubility in a range of common organic solvents—ether, dichloromethane, acetonitrile—hovers within tight bands batch to batch. Users scaling reactions from milligrams to kilograms gain predictability, cutting down on parameter adjustment cycles. Purity above 98% by chromatographic assay is our routine output, with most lots clearing 99%. We back these numbers up with regular instrumentation—NMR, GC-MS, FTIR—and supply the raw data alongside finished product. This is not a checkbox exercise. The end goal stays clear: let your synthetic route proceed without interruption or ambiguity.

    Product Handling and Quality Longevity

    Everyone producing and working with halogenated furans keeps an eye on aging effects. These molecules can color-shift, hydrolyze, or gunk up equipment if left exposed or sealed incorrectly. We maintain low-moisture, low-oxygen environments from final distillation to shipment. We have years of experience that go into every storage container. Chemists who have spent late nights scrambling to recover product from substandard batches know the risks—decomposition turns a crystal-clear liquid brown, and even a trace amount of hydrobromic acid will send LCMS baselines askew.

    We send every batch out in bottles purged with dry nitrogen, stopping trace oxidation and hydrolysis before they happen. For regular users, we offer customized bottle sizes to minimize how often the reagent is exposed to air. We’ve worked with both large pharma and lean startups to supply quantities that suit both screening campaigns and scaled production—here, waste reduction means more than cost savings; it preserves compound integrity. Long-term users match our batch records up with their own stability data—we share ongoing analysis to support validation cycles, and we’re always open to requests for expanded testing where new regulatory environments require.

    Supporting Applications That Matter

    Research groups taking on challenging syntheses often approach us for advice. Many want to maximize coupling yields, some need high reproducibility for process transfer, and some push completely new reactivity boundaries. Since 2,5-Dibromofuran packs two sites for substitution, you get a clear canvas for divergent chemistry—one that mono- or tri-substituted alternatives can’t provide. This dual-substitution position unlocks both rapid convergence and controlled sequential assembly, turning a simple input into a complexity engine.

    Our production runs have supported projects from small-molecule probes to early-stage pharmaceuticals. We’ve seen it fill a critical need in ring expansion reactions, bioactive scaffold assembly, ligand design for catalysis, and even liquid crystal material innovation. Many times, chemists have flagged up the way some batches from alternate suppliers can leave trace acid or colored solids after transfer—ruining entire runs by fouling columns or quenching Sensitive intermediates. We focus every process and every shipment on avoiding these pitfalls, always closing the feedback loop between end-user experience and our production discipline.

    Comparing to Alternatives and Missteps to Avoid

    Where generic 2-bromofuran finds a place, it usually restricts later manipulation to a single point on the ring. In contrast, the symmetrical dibrominated version lets you orchestrate two independent reactions or stage substitutions that require orthogonal protection and selective deprotection. We see the difference this makes when scaling: step economies pile up; chops off hours and columns from the work-up phase.

    Tri- or tetra-bromo derivatives bring in too much reactivity—side reactions climb and synthetic flexibility vanishes. We’ve stepped in on several campaigns to troubleshoot failed multi-brominated furan runs, pinpoint impurities by LCMS, and walk process chemists through switching to 2,5 for better yields. Unlike iodinated alternatives, dibromofuran strikes the right balance between reactivity and stability—iodine can overwhelm many catalytic systems and brings higher cost per gram, while chlorinated analogs lose coupling reactivity for difficult substrates.

    Customers sometimes ask about sustainability concerns. Bromine chemistry comes with environmental and safety baggage. We’ve adopted in-house, closed reactor loops to minimize worker exposure and strictly control bromine emissions. Our furan intermediates route through OECD-compliant supply chains, and we operate under permits that exceed the local safety code minimums. It’s not just a quality or cost question—it’s about securing confidence that the compound you’re working with doesn’t leave hidden burdens upstream or downstream.

    Putting Our Aims into Action

    Everything we’ve learned about handling, packaging, and delivering 2,5-Dibromofuran feeds straight back into how we serve the community. Our teams actively work with customers to improve their lab intake procedures—minimizing risk of air and moisture ingress, flagging compatibility with secondary reagents and containment best practices. We have solutions for operations needing single-use vials, bulk containers, or straightforward regulatory support for new drug filings.

    Many of our customers run multi-site operations and depend on repeatable order-to-order performance. We’ve adjusted logistics to meet these needs, and can manage both just-in-time deliveries and contract-driven batch reservations. In modern R&D, timelines go tight and windows for successful processing shrink each year. Real knowledge of how the product behaves—under a dozen different conditions, not just the one or two catalogued on a data sheet—pays off in reduced troubleshooting and speedier route optimization. Our technical support doesn’t just send PDFs; we connect real chemists with the folks who made every batch.

    Learning from Experience: The Human Element in Fine Chemicals

    Chemistry at the boundaries of what’s possible relies on the true substance behind every reagent. Our 2,5-Dibromofuran started as a small specialty item for academic collaborations. Over the years, requests grew as more groups unlocked creative ways to use the dual-bromine motif—libraries for fragment screening, macrocycle assembly, tunable materials for optoelectronics. Each expansion pushed our quality and logistics standards higher.

    Feedback from the field taught us the importance of details—grain size in crystals, seal tightness on caps, inventory turnover rates, and even minor pH shifts in deuterated solvents. Early lessons included learning the pitfalls of slow ground shipping or seasonal transit sensitivity; now, rapid air freight and thermal packaging come built into every service level. We stay close to the projects that use our products and evolve our processes when issues appear. That’s the value of working directly with manufacturers, not just through catalogs or anonymous logistics chains.

    The final results tell the whole story—smoother NMR, higher isolated yields, tighter purity specs, and happier chemists who can focus where it matters. From the moment a new lot leaves our reactor, it carries the proof of all the choices, from raw materials to final QC, made with your process in mind.

    The Impact Behind Reliable 2,5-Dibromofuran

    Every batch we send out stands for high standards and human oversight. Reliable dibromo intermediates make the difference between wasted time and direct progress. Whether building out a library, pursuing a new target in drug discovery, or scaling a material innovation, predictability brings results—every serious lab knows the feeling of opening a bottle and seeing liquid, color, documentation, and cleanup go exactly as planned. We included customers in our development process by listening carefully to their problems, running extra tests, and solving issues long before they bottlenecked downstream work.

    Great chemistry comes from more than just good molecules. It’s about knowing every input meets or exceeds technical goals, so the best ideas in the lab become the best results in the field. 2,5-Dibromofuran—from its synthesis and purification to every bottle delivered—reflects years of those lessons, every lot built from the ground up by people who care about details and know the stakes. We’re proud of the difference our hands-on approach makes in every vial, and we remain committed to driving innovation and reliability for every project we touch.