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2,5-Dibromothiophene

    • Product Name 2,5-Dibromothiophene
    • Alias 2,5-Dibromothiophen
    • Einecs 221-835-8
    • 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
    VTB
    Specifications

    HS Code

    398164

    Cas Number 3141-27-9
    Molecular Formula C4H2Br2S
    Molecular Weight 241.93
    Appearance Colorless to pale yellow liquid
    Boiling Point 226-228°C
    Melting Point -7°C
    Density 2.082 g/cm³
    Purity Typically ≥98%
    Refractive Index 1.627
    Flash Point 104°C
    Solubility In Water Insoluble
    Smiles C1=C(SC=C1Br)Br
    Inchi InChI=1S/C4H2Br2S/c5-3-1-2-4(6)7-3/h1-2H

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

    Packing & Storage
    Packing Amber glass bottle labeled "2,5-Dibromothiophene, 98%, 25g" with hazard symbols and tightly sealed screw cap for safe storage.
    Shipping 2,5-Dibromothiophene is shipped in tightly sealed containers, protected from light, moisture, and incompatible substances. Transport follows international chemical safety regulations, including appropriate labeling and documentation. Containers are handled carefully to prevent breakage, and shipping is typically restricted to authorized carriers specialized in hazardous materials. Suitable temperature controls are maintained during transit.
    Storage 2,5-Dibromothiophene should be stored in a cool, dry, and well-ventilated area away from sources of ignition and incompatible substances such as strong oxidizers. Keep the container tightly closed when not in use and protect it from light and moisture. Use only in a chemical fume hood and store in a dedicated chemical storage cabinet designed for organic chemicals.
    Application of 2,5-Dibromothiophene

    Applications of 2,5-Dibromothiophene in Industrial Manufacturing

    2,5-Dibromothiophene is a key halogenated intermediate widely applied in several high-value industrial sectors. Its reactivity and controlled substitution pattern support advanced synthesis needs in specialty chemicals, pharmaceuticals, electronics, and agrochemical manufacturing.

    1. Building Block for Pharmaceutical Intermediates

    Pharmaceutical manufacturers utilize 2,5-Dibromothiophene in the synthesis of thienyl-based drug intermediates, particularly for anti-inflammatory, antiviral, and central nervous system actives. Its dual bromine positions enable selective cross-coupling reactions, such as Suzuki and Stille coupling, forming tailored heterocyclic scaffolds. Application volumes respond to compound-specific route design and patent strategy for API synthesis, making it valuable for both new molecular entities and generic process development.

    Industry compliance standards

    • ICH Q7A GMP for Active Pharmaceutical Ingredients
    • EU EudraLex Volume 4 GMP guidelines
    • FDA 21 CFR Part 211 (Finished Pharmaceuticals GMP)
    • USP, EP, JP Residual Solvent & Impurity Guidelines

    Typical usage ratio

    • 5–18% by input molar ratio for core heterocycle formation; adjusted depending on desired functionalization and in-process yields

    Downstream process integration

    • Enters process after initial halogenation or thiophene ring synthesis; serves as a direct substrate in cross-coupling to form target intermediates
    • Undergoes Pd-catalyzed couplings, hydrogenation, or additional alkylation to reach final active structure
    • Subject to phase transfer and chromatographic purification for API-grade quality

    Final product types

    • Active Pharmaceutical Ingredients with thienyl substructures (e.g., epilepsy, flu, anti-inflammatory APIs)
    • Advanced pharmaceutical building blocks for CNS drugs
    • Key intermediates for anti-viral pipelines under clinical development

    2. Precursor for Organic Electronic Materials

    The production of organic electronic materials, such as organic semiconductors and thin-film transistors, incorporates 2,5-Dibromothiophene for synthesizing high-purity oligothiophenes and polythiophenes. Its controlled bromination pattern enables precise polymer growth through Grignard metathesis or Kumada coupling. This improves batch-to-batch uniformity and electrical performance in devices and increases material yield for optoelectronic applications.

    Industry compliance standards

    • IEC 62660 (Secondary lithium cells and batteries safety)
    • RoHS Directive (2011/65/EU) for hazardous substance limitation
    • REACH Regulation (EC) No 1907/2006 for chemical safety
    • Customer-specific materials purity specifications (typically >99.5%)

    Typical usage ratio

    • 8–22% of total monomer feed, adjustable through reactor design and end polymer chain length requirements

    Downstream process integration

    • Added post-synthesis of the thiophene core, involved in monomer activation via lithiation, followed by chain extension or cross-coupling polymerization
    • Works as an end-capper or initiator for controlled polymerization, ensuring targeted molecular weight and solubility
    • Processed through solvent or vapor deposition for device fabrication

    Final product types

    • Organic thin-film transistors (OTFTs)
    • Organic photovoltaic materials (OPVs)
    • Conducting and semiconducting polythiophenes for flexible displays and sensors

    3. Intermediate in Agrochemical Synthesis

    2,5-Dibromothiophene is critical in producing active thienyl-based agrochemicals, including fungicides and herbicides. Its reactivity profile favors selective coupling and functionalization, supporting innovations in resistance management and low-residue formulations. Agrochemical manufacturers value its reproducibility for scaling up pilot and commercial batch processes under strict regulatory review.

    Industry compliance standards

    • FAO/WHO Codex Alimentarius for pesticide residues
    • ISO 9001:2015 for quality management in agrochemical synthesis
    • EPA 40 CFR Part 180 (US pesticide tolerances)
    • China GB 2763 Maximum Residue Limits for Pesticides

    Typical usage ratio

    • 12–30% by precursor mass, optimized for target molecular substitution and yield in multi-step agrochemical routes

    Downstream process integration

    • Introduced after initial ring synthesis; participates in halogen exchange or nucleophilic substitution to generate unique active moieties
    • Processed with copper- or palladium-catalyzed methodologies to install side chains or additional heteroatoms
    • Transferred to downstream formulation plants for dilution and EC/SC product finalization

    Final product types

    • Thienyl-based herbicides (e.g., for broadleaf weed control)
    • Fungicidal active ingredients (for cereals, fruits, vegetables)
    • Intermediate precursors for further agrochemical innovation

    4. Advanced Material Synthesis for Specialty Polymers

    Manufacturers in specialty polymers employ 2,5-Dibromothiophene to introduce rigid, conjugated segments into polymer backbones for enhanced thermal stability and mechanical strength. It enables step-growth or controlled radical polymerization, where regioregularity and stereochemistry are central to downstream performance. This application is essential for producing engineering plastics and functional coatings with tailored electrical or barrier properties.

    Industry compliance standards

    • ASTM D638/D790 for mechanical property testing
    • ISO 10993-5 (biocompatibility, as required for medical contact or packaging)
    • UL 94 (flammability rating for specialty polymers)
    • REACH SVHC compliance for polymer additives

    Typical usage ratio

    • 3–12% of total monomer input; precise dosing based on polymer architecture and desired property balance

    Downstream process integration

    • Integrated after oligomer preparation; enters as a di-bromo crosslinker or chain extender via nickel- or palladium-catalyzed condensation reactions
    • Coupled with dithiols, diamines, or other halides according to the functional group compatibility of end-use requirements
    • Subject to purification and compounding before pelletization or direct molding

    Final product types

    • High-performance engineering plastics for automotive and electronics
    • Conductive specialty coatings
    • Polymer films with customized gas or vapor barrier properties
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    Certification & Compliance
    More Introduction

    2,5-Dibromothiophene: Proven Reliability from a Manufacturer’s View

    At our plant, turning thienyl compounds into reliable, high-purity building blocks isn’t just a job. We’ve learned to respect each step, because the way you make something like 2,5-Dibromothiophene defines how it performs years later down a production line. Now that more research teams focus on specialized organobromine intermediates, we see more discussion about purity, isolation, and environmental impact. Let’s talk directly about what matters for chemists and manufacturers using this compound, pulling from day-to-day experience making plenty of it—every batch an opportunity to get things right.

    Our View on Production: Purity, Consistency, and What Sets 2,5-Dibromothiophene Apart

    Synthesizing 2,5-Dibromothiophene (C4H2Br2S, CAS 3141-11-9) at industrial scale sits at a crossroads between legacy chemistry and the new green mandates. Our process uses thiophene as the starting material with controlled bromination under protection from moisture and air. We keep reaction temperatures steady and close off all oxygen exposure to minimize byproducts—details that seem minor on paper but protect your final products downstream.

    Customers often ask where this material fits compared with mono-brominated or 2,4-dibromothiophene analogs. Take a closer look at why the specific dibromo substitution at the 2 and 5 positions works so well. First, direct substitution at these points keeps the aromatic character of the ring without over-activating the system toward polymerization or unwanted coupling. That stability gives you a predictable platform for cross-coupling or Grignard reactions. Some labs use mono-brominated thiophenes, thinking they’re more selective—but handling, volatility, and lower reactivity hold them back in more complex syntheses.

    Every customer wants reliable reactivity, so we prioritize high-purity crystallization and minimize trace metals. That costs more than rough-and-ready technical grades, but even minor contamination ruins downstream Suzuki couplings. We’ve run split tests where grams of less-pure material choked a reaction that runs smoothly with our cleaner-grade product. We do not add excipients or stabilizers, so the customer knows exactly what enters their reactor—plain old 2,5-Dibromothiophene, nothing else.

    Why Chemists Choose 2,5-Dibromothiophene

    From the manufacturer’s floor, the main draw of 2,5-Dibromothiophene is its predictable halogenation and readiness for modern cross-couplings. This ring system acts as a flexible handle in organic electronics, pharmaceuticals, and advanced polymers. During meetings with formulation teams, we’ve heard direct feedback: when our material meets strict GC-MS analysis—99.5% area purity, single-digit ppm potassium and iron—the results improve, yield rises, and post-processing becomes less of a headache.

    Consider researchers exploring OLED materials who aim for high photostability and custom band-gaps. They need dibromo-substituted cores to form symmetric structures through Stille or Suzuki coupling. 2,5-Dibromothiophene gets chosen because both bromines activate at similar rates, so reaction control is tighter. With something like 2-bromothiophene, the asymmetry drives side reactions and messy mixtures. Our colleagues in API and fine chemical synthesis mention the same thing: if you want to split a thiophene ring in two for downstream functionalization, this compound lines up better than any alternative. That opens the door for making custom monomers for high-technology, light-emitting applications that we all hear about in trade journals—but rarely see in action.

    Honest Challenges and Real Solutions: Manufacturing Realities

    Any plant operator knows the challenges behind batches that don’t meet purity specs. Moisture triggers byproducts. A slight slip in handling bromine swings the product distribution and makes purification tough. Our shop learned, after several failures back in the day, to run bromination under nitrogen and use very dry solvents. It’s small stuff like this, but the bitterness of watching a full batch go off-spec the old way lingers.

    Some customers have real concerns over residual solvent and elemental impurities, especially where their regulator or procurement agent asks for full supporting paperwork. We invested in glass-lined reactors and added real-time headspace monitoring for bromine loss. We track not just the GC-MS but also ICP for metals and Karl Fischer for water. If you’ve ever lost a run because someone skipped a drying step, you get why we do it this way.

    We’re not a boutique lab or a backroom trader—we cycle many kilograms per run, and every single kilo that misses target puts hours of preparation under the microscope. Even with all that, we still have to control exposure to both workers and wastewater. So, we set up absorbers for bromine fumes and handle off-gas with caustic scrubbers, not just venting. Waste streams from halogenated syntheses take real maintenance to avoid local compliance issues.

    What Sets Industrial-Grade Material Apart

    When buyers see a drum of 2,5-Dibromothiophene, they’re used to assuming dry tan or yellow solid, free-flowing and with low residual solvent. Technical grade material made quickly often ends up clumpy or sticky. That affects handling in automated systems. We take deliberate extra time in vacuum drying, checking every batch for loss on drying and shifting it back through the system if anything’s amiss. Some people say those small details don’t matter, but we’ve seen whole product lines ruined by poor drying. Downstream processors using extruders or precision metering systems appreciate when every kilo scoops and pours the same way, batch after batch.

    Compared to differently substituted thiophenes—say 3,4-dibromo or 2,4-dibromo—the 2,5 analog delivers sharper, cleaner chromatographic behavior, easier scale-up, and greater substrate compatibility. Those minor differences start to add up at 100+ kilo orders, not just at the lab scale.

    Practical Applications: Who Uses This, and How

    Plenty of demand comes from research teams scaling from a few grams to pilot-plant runs. Most of the material ends up in organic electronics—think OLED devices or intermediate layers for printed circuit boards. Specialty pharmaceutical suppliers grab it for functionalizing heterocyclic rings, preferring 2,5 over 2-only bromo for symmetry and yield improvements. In polymers, the symmetrical substitution makes for more regular architectures and improved material properties, like conductivity for high-performance plastic electronics.

    Several customers have pointed to one use case that best highlights the difference: using 2,5-Dibromothiophene as a key intermediate for polymerizing polythiophenes. PCBs, sensors, and flexible conductors benefit from uniform, reproducible polymer chains. Substitution at 2,5 means less branching and fewer defects, so final electrical characteristics stay tight across lots. Technical managers working on long-term deployment want that guarantee, preferring to pay for quality up front than troubleshoot failed devices a year after delivery.

    Others working in agrochemical building blocks point out that symmetry in the dibromo thiophene core leads to predictable downstream derivatization. The 2,5 arrangement provides an even platform to attach side chains or more complex groups, crucial for tuning biological activity. Anyone who’s ever run a late-stage functionalization on an unsymmetrical ring knows the headaches that brings—unwanted isomers, tough purification, lower yields.

    Having spent years handling order volumes for both pharmaceutical and electronics manufacturers, one thing stands out: reliability matters more than anything. Nobody wants a batch to stall because of undetected residuals or a subtle difference in reactivity. The market for specialty organobromines keeps evolving, but our conversations never stray far from on-spec, high-purity basics.

    A Word About Safety, Handling, and Traceability

    Since we produce in industrial volumes, we have firsthand experience with detailed material tracking. We document all raw material origins and test every drum for both purity and batch-specific traits. Any deviation—color, flow, moisture—spots a red flag investigated before dispatch. This discipline grew out of necessity, after early shipments back in the day led to some hard lessons when a lower-grade input cost a client weeks of rework.

    Shipping halogenated aromatics brings strict import/export handling rules. We remotely validate packaging for leak-proof seals, robust enough for international transit. Plenty of local authorities now want direct supply lines so they can track the chain of custody back to us. Every shipment includes lot tracking and full analytical data, not just a slip of paper with the molecule and batch weight. Traceability doesn’t just keep us inline with regulations; it protects end-use reliability. Chemists in downstream labs value transparency for batch-to-batch reproducibility and to satisfy the ever-tightening compliance checks.

    We also monitor working environments everywhere 2,5-Dibromothiophene is stored, since it releases a telltale sharp odor above room temperatures. Closed transfer systems now keep workers safer, with proper ventilation as a backup. Regular operator briefings and spot-checks prevent the rare accident before it happens, and waste collection aligns with the best practices for halogenated organic remnants. Wastewater from these syntheses needs careful management to avoid local environmental problems, so we set up multi-stage collection and treatants to strip free bromine before sending outflows to our treatment plant. Regulatory agencies ask us to log these processes, and we go above simple logbooks—continuous monitoring provides feedback we trust ourselves.

    Direct Differences: 2,5-Dibromothiophene vs. Other Thiophenes and Brominated Intermediates

    Not all brominated thiophenes handle or react the same way. From years dealing with mixtures in the lab, we’ve seen certain traits come out in side-by-side testing. Mono-brominated versions like 2-bromothiophene tend toward volatility, off-gassing more easily, and reacting unevenly during complex couplings. Triple- or more heavily halogenated thiophenes add cost, fouling catalysts and complicating purification—nobody’s thrilled about dealing with sticky byproducts or shrunken yields.

    Our experience shows 2,5-dibromo versions stabilize well without creating excess side-products. Each synthetic path has its quirks, but symmetrical substitution holds up in both oxidative and palladium-catalyzed reactions. Customers working with unsymmetrical rings often call back for technical assistance—they think swapping in a “similar” brominated thiophene will lead to comparable yields, but lab trials surprise them. The electron distribution and activation energy profiles just do not match up, so they land on the tried-and-true 2,5-dibromo route.

    Sometimes buyers look for less expensive, technical-grade dibromothiophenes from bulk vendors, but the downstream pain rarely justifies the savings. Extra cost creeps in later: failed runs, equipment downtime, employee exposure to messier, less controllable reactions. We fielded urgent requests for emergency re-supply after clients started with lower-purity lots from elsewhere—one mishap with off-gassing convinced them to switch permanently to high-spec supply.

    Evolving Demands: What End-Users Keep Asking

    Over the last five years, requests for tighter impurity limits and more flexible logistics led us to rethink core parts of our operation. Early deliveries to multinational R&D hubs brought home how far documentation standards have risen. Now, every shipment includes a thorough analytical package—high-fidelity NMR, mass spec, and single-digit ppm metals. Whenever the market asks for lower environmental impact, we target greener solvents, solvent recovery for bromination, and closed-loop packaging.

    The profile of the average user keeps changing as we speak. Teams from electronics, pharmaceuticals, and new materials screen more potential inputs, always requesting cleaner, more predictable batches. Smaller customers, too, who previously adapted to whatever supply they could find, now demand formal validation. That means our own supply chain—bromine procurement, solvents with verifiable origins, logistics routed around environmental bottlenecks—has turned into as much of a differentiator as the molecule itself.

    Having direct feedback from so many product launches, scale-ups, and regulatory audits continually challenges us to improve. We work with technical managers in each industry to tune analytical test panels, run pilot trials in our own sample reactors, and gather failure mode histories. The goodwill earned by sharing this “inner factory life” with partners forms the single strongest selling point. Buyers know they’re getting reliability, not just a formula and a purity grade, because our process stays transparent and consistent.

    Adapting to a Greener Outlook

    Traditional bromination processes often generate waste and pose hazards. Over the last decade, increased environmental oversight forced serious upgrades. Implementation of closed-loop bromine recovery and solvent recycling handled a large portion of the issue. Our site added real-time air and water monitors with direct data export to plant managers for quick intervention should limits get exceeded. Waste bromine and contaminated solvents no longer enter open wastewater—they get stripped, neutralized, and precisely metered off for licensed disposal.

    Green chemistry isn’t just a label. Switching to less toxic solvents in the early stages cut side-product formation significantly. That switch didn’t come easy—several iterations of the process gave us slower reaction rates, but with fine-tuning, yields matched legacy methods. Energy-efficient drying and longer vacuum holds cost a bit more upfront, but product storability benefits paid off long-term. Regulators now ask for lifecycle analysis and energy-plus-material intensity data for every kilogram produced, so we track and report it directly.

    Solvent reuse and secondary brine management avoid the major pain points for customers worried about supply chain ESG impact. The more that consumer tech and drug companies require proof of ethical sourcing, the more these behind-the-scenes changes matter. Without real investment in cleaner, safer ways to make these compounds, we’d fall behind. The skilled operators in charge of batching and purification know every aspect of the “cleaner” processes—their experience with traditional chemistry anchors the operation, and the tweaks for modern compliance come straight from years on the shop floor.

    Customer Service: What Years of Feedback Teach

    No one orders 2,5-Dibromothiophene just to sit on a shelf. Every kilogram heads for something that matters downstream. Logistical flexibility ended up critical—many customers work across different time zones and have tight on-demand schedules. Fast communication and custom-sized shipments, whether drums or smaller packs, add practical value. We learned from early feedback that standardized packing never fits every site. Some places require air-tight bins; others need vacuum-packed liners.

    Years spent in customer support taught us patience and thoroughness. If a client reports trouble with mixing or an unexpected residue, we pull records and offer a fresh sample for investigation. Early root-cause analysis avoids recurring pain points, and being up front about possible batch anomalies builds trust. The same internal teams who manage reactors answer technical requests—nobody reads from a generic help sheet or passes the customer down a chain. Fielding these calls led to better packaging ideas and improved both our product and service.

    The Road Ahead for 2,5-Dibromothiophene Sourcing

    Manufacturing at scale sharpens appreciation for the small, persistent improvements—relating the daily grind of synthesis to the high-precision demands of tomorrow’s devices and APIs. Each advancement in the plant directly flows to every end user. The industry’s shift toward electronics, new drug scaffolds, and more sustainable approaches means more focus on the reliability of supply and the integrity of every batch. Instead of a commodity, 2,5-Dibromothiophene acts as a crucial, specialty intermediate—easy to underestimate but impossible to replace when downstream performance matters.

    We remain convinced, as those running reactors and tracking shipments, that getting it right every single time—tight impurity controls, complete documentation, responsive supply—offers the best support to the researchers, engineers, and developers counting on us. Every gram of 2,5-Dibromothiophene we ship represents thousands of hours perfecting process and quality, drawing on the collective expertise of chemists who keep the machinery running and the next innovations moving forward.