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2,5-Dichlorothiophene

    • Product Name 2,5-Dichlorothiophene
    • Alias 2,5-Dichloro-2,5-dihydrothiophene
    • Einecs 215-109-3
    • 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
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    Specifications

    HS Code

    365449

    Name 2,5-Dichlorothiophene
    Cas Number 882-34-8
    Molecular Formula C4H2Cl2S
    Molecular Weight 169.03
    Appearance Colorless to pale yellow liquid
    Boiling Point Celsius 194-196
    Melting Point Celsius -7
    Density G Ml 1.482
    Flash Point Celsius 80
    Refractive Index N20 1.584-1.586
    Smiles C1=C(SC=C1Cl)Cl
    Solubility Insoluble in water; soluble in organic solvents

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

    Packing & Storage
    Packing A 100 mL amber glass bottle securely sealed, labeled "2,5-Dichlorothiophene," includes hazard symbols, safety warnings, and batch details.
    Shipping 2,5-Dichlorothiophene is shipped as a hazardous chemical, typically in sealed, chemical-resistant containers to prevent leaks and contamination. Packaging complies with international transport regulations (e.g., UN, DOT, IATA). Proper labeling, documentation, and handling instructions—including hazard warnings—are provided to ensure safe transit and storage.
    Storage 2,5-Dichlorothiophene should be stored in a tightly closed container, in a cool, dry, well-ventilated area away from sources of ignition, heat, and direct sunlight. Keep it separated from oxidizing agents and strong bases. Store in a chemical-resistant, labeled container and ensure proper secondary containment. Use in a fume hood, and avoid exposure to air and moisture to maintain stability.
    Application of 2,5-Dichlorothiophene

    Applications of 2,5-Dichlorothiophene in Industrial Manufacturing

    2,5-Dichlorothiophene plays an essential role as a building block in multiple chemical manufacturing pipelines. Our customers leverage this intermediate to carry forward complex syntheses, precisely matched to downstream sector needs and regulatory frameworks. Below, we provide an overview of real-world manufacturing applications, reflecting current sector practice and compliance requirements.

    1. Pharmaceutical Intermediates Production

    Pharmaceutical manufacturers use this compound as a key intermediate in the synthesis of heterocyclic active pharmaceutical ingredients, including certain anti-infective and anti-inflammatory agents. The controlled substitution pattern allows for high-yield coupling in multi-step reactions. Integration into GMP-certified production lines requires careful monitoring during sulfonation, etherification, or further halogenation reactions to achieve consistent bioactive intermediates with traceable purity profiles, matching ICH guidelines for impurity control.

    Industry compliance standards

    • ICH Q7 (Good Manufacturing Practice for Active Pharmaceutical Ingredients)
    • USP/NF and EP monograph requirements for intermediates, where specified
    • 21 CFR Part 211 (GMP for finished pharmaceuticals, by extension of intermediates)
    • ISO 9001:2015 for process quality management

    Typical usage ratio

    • Typically 0.5–1.2 molar equivalents depending on the desired substitution; process scale-up may require stoichiometric excess, calculated based on downstream yield optimization and waste minimization.

    Downstream process integration

    • Charged into the primary reactor after initial charge of solvent and base; frequently reacts with nucleophilic partners under controlled heating in the 60–95°C range.
    • Introduced during early stage condensation or cyclization in API intermediate assembly.

    Final product types

    • Non-steroidal anti-inflammatory drug precursors
    • Bactericidal heterocycle derivatives
    • Advanced pharmaceutical building blocks exported to API facilities

    2. Agrochemical Synthesis

    Formulators in the crop protection industry utilize this dihalogenated thiophene in key synthesis steps for herbicides and fungicidal actives. Reactive chlorine atoms facilitate high-efficiency coupling or substitution with various nucleophilic agrochemical scaffolds. Compliance requires clean reaction profiles and validated impurity checks against regulated agrochemical actives, as raw material quality directly affects field application certification and environmental toxicity registrations.

    Industry compliance standards

    • FAO/WHO Specification and Evaluation for Plant Protection Products
    • OECD Guidelines for the Testing of Chemicals (relevant to synthesis steps and residue analysis)
    • ISO 17034:2016 (General requirements for reference material producers)
    • ISO 14001:2015 for environmental aspects in chemical production

    Typical usage ratio

    • 1.0–1.3 equivalent ratio as a core ring intermediate; specific loadings adjusted based on the downstream active formulation and process mass intensity requirements.

    Downstream process integration

    • Fed into batch or continuous reactors during ring assembly phase of triazole and pyrrole herbicides.
    • Used in nucleophilic aromatic substitution or Suzuki coupling reactions in late-stage actives production.

    Final product types

    • Triazole-based fungicides
    • Selective herbicide intermediates
    • Active ingredient concentrates for formulation houses

    3. Specialty Polymers and Conductive Materials

    Materials manufacturers select this dichlorinated thiophene as a monomer or as an advanced intermediate in the production of conductive polymers and specialty resins. The chemoselectivity of the two chlorine atoms offers precise points for chain extension and functional group incorporation, critical in optoelectronic or antistatic material development. Quality demands include REACH registration for use in the EU market and strict in-process controls to validate molecular weight distribution and electrical property consistency in the finished polymer matrix.

    Industry compliance standards

    • REACH Regulation (EC) No 1907/2006 for chemical registration and SVHC assessment
    • RoHS 3 Directive (EU) 2015/863 for electronic materials
    • ISO 9001:2015 for quality systems
    • ISO 14001:2015 for sustainable production interfaces

    Typical usage ratio

    • Ranges between 5–20% by weight in co-polymerization reactions depending on desired end-use conductivity, thermal stability, or resin flexibility; usually determined by target polymer architecture.

    Downstream process integration

    • Charged directly into the polymerization reactor with co-monomers such as thiophene, furan, or bithiophene derivatives for oxidative or metal-catalyzed polymerization.
    • Employed as an end-capping agent in specialty resin synthesis for anti-static coatings and conductive films.

    Final product types

    • Electrically conductive polymers for wearable electronics
    • High-performance resins with antistatic properties for packaging and device housings
    • Specialty coating additives for automotive and aerospace industries

    4. Organic Light-Emitting Diode (OLED) Material Manufacturing

    OLED display material developers incorporate dichlorothiophene derivatives to engineer high-purity emitters and hole transport layers. The carefully controlled halogenation permits selective functionalization, producing intermediates that determine emission wavelength and stability profiles. Regulatory adherence includes global chemical inventories such as TSCA and K-REACH, alongside rigorous optical and purity validation demanded by end-user device manufacturers.

    Industry compliance standards

    • TSCA (Toxic Substances Control Act, USA) inventory registration
    • K-REACH (Korea Registration, Evaluation and Authorization of Chemicals)
    • IEC 62321 for determination of certain substances in electronic products
    • ISO 9001:2015 for supply chain quality assurance

    Typical usage ratio

    • Employed at 2–8% by mol in emitter or transport layer production; loading specified by molecular design of the OLED stack and colorimetry targets.

    Downstream process integration

    • Dosed during Suzuki, Stille, or Buchwald-Hartwig coupling steps to create π-conjugated systems for thin film deposition.
    • Processed further through chromatographic purification prior to device integration steps.

    Final product types

    • Blue and green emitter intermediates for mobile device displays
    • Hole transport layer precursors for OLED screens
    • Custom organic semiconductors for research and development

    5. Advanced Dye and Pigment Synthesis

    Producers of specialty dyes and pigments apply dichlorinated thiophenes for constructing chromophores with targeted color stability and solvent resistance. The molecular scaffold allows for directed halogen substitution and subsequent sulfonation or amination, necessary to achieve high-performance pigment properties. Integration into downstream syntheses warrants compliance with global chemical use standards, and batches undergo both colorimetric validation and heavy metals screening to meet customer import standards.

    Industry compliance standards

    • EN 71-3 (Migration of certain elements from toy and dye applications)
    • REACH Annex XVII restriction on hazardous substances
    • ISO 787-1 for pigment characterization and testing methods
    • ASTM D476 for pigment classification and identification

    Typical usage ratio

    • 0.8–5% molar basis in chromophore backbone assembly; ratio tuned by shade intensity, intended application (e.g., plastics vs. inks), and end-use solvent compatibility.

    Downstream process integration

    • Introduced as a key starting material during initial condensation or cyclization for azo, phthalocyanine, or quinacridone dye synthesis
    • Reacted under catalysis to establish stable pigment structures compatible with high-temperature or solvent-intensive processing lines

    Final product types

    • Solvent-resistant dyes for automotive and industrial coatings
    • High-color-strength pigments for textile printing
    • Fastness-grade colorants for plastics extrusion
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    Certification & Compliance
    More Introduction

    2,5-Dichlorothiophene: Reliable Chemistry for Modern Applications

    Practical Value in Every Batch

    Experience guides every decision in our manufacturing plant, and over the years, 2,5-dichlorothiophene has proven essential when reliability and purity matter. Our team knows firsthand how subtle differences in synthesis impact downstream reactions. Each batch we produce delivers genuine consistency in color, purity, and odor. We run HPLC and GC for every lot. In our line, we keep chlorinated thiophenes like this one isolated from unrelated substances, so cross-contamination never threatens your formulation.

    Honest Results in the Plant

    Our process produces 2,5-dichlorothiophene with high GC purity. We use a sealed vessel system that controls atmospheric contaminants and water ingress—two factors that have ruined yields for some outside labs we’ve visited. Our chemists regularly test trace chloride and look for sulfur residues with stringent internal controls. Over time, we have adjusted reaction temperatures and phase transfer catalysts to suppress side reactions, so the chlorination hits the intended sites on the ring every cycle. This reduces tarry byproducts and keeps our mother liquor easy to recycle, which keeps production lines moving without messy downtime.

    Model: 2,5-Dichlorothiophene C4H2Cl2S

    We have standardized our output to meet end-user requirements: high assay, consistent melting point, and colorless to pale yellow appearance. Reactions tend to run trouble-free with this input. The model, 2,5-dichlorothiophene, contains two chloro groups at the 2 and 5 positions of the thiophene ring, giving it reactivity that’s more predictable than other isomers. Chemically, this means downstream bromination or coupling often requires less workup, lowering time and solvent use. That matters most in commercial-scale synthesis, where every hour spent reworking a batch adds up.

    How Customers Actually Use It

    The reality in manufacturing is you want an input to behave as expected. Our customers in pharma and agrochemical sectors take 2,5-dichlorothiophene as a building block—specifically for constructing complex organic molecules where a double-chlorinated, sulfur-containing ring acts as a rigid anchor. Medicinal chemists find it indispensable for certain heterocyclic scaffolds. In practice, they couple, alkylate or brominate at specific sites. In crop science, a reliable supply of this chlorothiophene ensures that actives can be scaled from a few grams to hundreds of kilos without running into bottlenecks from off-quality feedstock.

    Chlorination patterns in this molecule improve selectivity for Suzuki, Stille, and Buchwald–Hartwig coupling reactions. These are the tools that our partners rely on daily. The high stability of this isomer means process chemists can handle it without extra personal protective equipment or retooling their lines. Our QC records regularly show less batch-to-batch variability than found in non-standardized or trader-sourced dichlorothiophenes.

    Spotting the Differences: Not All Thiophenes Are Created Equal

    Having worked through enough pilot trials, our team has seen the outcomes when customers substitute other chlorothiophenes for 2,5-dichlorothiophene. Products like 2,3-dichlorothiophene or 2-chlorothiophene look similar on a supplier’s list, but differences in reactivity and impurity profiles matter more than the catalog would suggest. 2,3-Dichlorothiophene introduces meta-positioned chlorine atoms, which leads to poor yields in certain key couplings due to regioselectivity issues. Monochlorothiophenes offer even fewer synthetic options.

    Our combustion analysis, IR spectra, and NMR data highlight clear distinctions—2,5-dichlorothiophene enables functionalization at the correct sites. By contrast, alternative isomers tear down efficiency and force chemists to engage in repeated purifications. The genuine cost is time, as well as extra waste and solvent consumption. That’s a frustration any plant manager wants to avoid. With 2,5-dichlorothiophene, you get a reagent that reduces these headaches.

    Why Purity and Handling Win Out

    We have learned from both failures and successful large-scale runs that storage and drum handling shapes the quality that reaches our customer’s line. We fill only after multi-stage vacuum drying and nitrogen blanketing. This reduces risk of hydrolysis, which otherwise produces off-odors and color bodies that can block process lines. By keeping oxygen and moisture out, our product retains its transparency and doesn’t develop the black streaks or tar seen in poorly protected drums from other sources.

    Internally, we have invested in modern filtration and reactor linings that don’t leach ions into the product. In years past, we struggled with metallic residues from glass-lined vessels. Today, our process upgrades safeguard purity and give us the low ppm impurity rates major pharma clients now check for. This isn’t a vanity metric; repeat runs prove that process yields increase when clients use clean, pure starting material. That edge is why our chemical engineers stick to robust, repeatable procedures.

    Performance in Complex Reactions

    Take C–C coupling as an example. Process chemists often report variable yields and unreproducible color in their end product when using generic dichlorothiophenes. Our 2,5-isomer stands apart in both lab-scale and plant batch. Repeated TLC and analytics show tighter Rf values, allowing for easier separation. This lets our customers reduce their solvent load and shrink overall process time, translating directly into cost savings.

    Real-world accounts show the difference. One agrochemical group used to fight a haze forming in their reactor after running couplings with non-specific dichlorothiophene. Once they switched to our material, the haze disappeared—chromatograms came back clean, and they were able to skip a column step. Efficiency means less waste and quicker scale-up, helping them beat delivery schedules without quality worries.

    Taking Responsibility Across the Line

    Producing any chlorinated aromatic raises EHS questions, and we tackle these head-on. Our manufacturing floors feature closed-loop vapor recovery, and temperature-controlled reactors minimize fugitive emissions. We have always prioritized in-house process safety, not just when inspectors visit but every shift. Workers wear appropriate PPE for chlorinated compounds, and exhaust is treated with activated carbon bed scrubbers. Solvent management now recycles more than 85 percent of input, keeping our waste load lighter. Incinerables go to certified handlers, tracked with every shipment.

    We built these systems after direct feedback from operators and project chemists—not management memos. The result? Lost-time incidents and unplanned emissions have dropped sharply since 2020, helping both our staff and our local community. Those protections extend even after the product leaves our gate. We offer guidance to customers on safe drum storage and movement, and we welcome their EHS audits of our plant. Accountability doesn’t end with the invoice.

    Applying Knowledge: Engineering Better Outcomes

    We’ve worked on enough joint development projects to know what matters: time, cost, compliance, and performance in the final formulation. Our team consults on scale-up work, troubleshooting, and process intensification. In one recent collaboration with a pharmaceutical group, we reduced the number of crystallizations needed for a key intermediate by dialing in a tailored drying profile for our 2,5-dichlorothiophene batch. End result: regulatory submissions succeeded because impurity carryover dropped below the demands of the client’s template.

    In a plant setting, this kind of practical advice counts. We aren’t afraid to share what didn’t work on our own lines, because that honesty saves resources at your facility. If a particular base or solvent gives rise to side products, we let the customer know. Sometimes raw material from a distributor looks fine on the certificate of analysis, but downstream sticking points show up—emulsions, color, heavy end residue. Through root cause analysis, we help users decide how to tweak their process or adjust storage routines, drawing on both analytic data and decades of chemical plant know-how.

    Supporting Scale and Speed

    Speed remains a hallmark of industrial delivery. Downtime on a batch reactor or lost yield on a campaign hits your bottom line just as hard as anyone else’s. As a direct manufacturer, we can align production to your actual schedule. Our facility runs year-round, and we stock volumes that accommodate both monthly drum lots and larger bulk requirements. Coordination with logistics partners and real-time batch release speeds up response times. In an industry where lead times often stretch due to supply chain uncertainty, having a manufacturing partner with actual inventory can keep your timelines intact.

    Every day, our plant supervisors talk with customers about scheduling, special packing needs, and shipment timing. We don’t rely on layers of middlemen or vague commitments. Instead, we keep lines of communication open and prioritize transparency, which our partners tell us minimizes the surprise disruptions that traders or non-manufacturers often can’t control.

    Continuous Improvement, Based on Living Experience

    A chemical plant can’t stagnate. Our drive to deliver better 2,5-dichlorothiophene led us to incremental process improvements: modern automation on the reaction sequence, advanced filtration, and more effective solvent recovery. Each change starts on our R&D line, where our chemists and engineers test under real production conditions. We make adjustments only after confirming gains in repeatability and cost control. These aren’t marketing claims—they appear in our utility savings, in cleaner drum samples, and in customer plant trials.

    We also field technical questions from users around the world. Some new applications emerge from unexpected corners—materials science or specialty polymers—where a unique halogenated thiophene serves as a building block for advanced electronics or light-emitting devices. By maintaining a close dialogue, we learn what properties matter most: purity, lot size, solvent compatibility, or crystalline habit. Our product evolves in response to this feedback, driven by the collaborative nature of industrial chemistry.

    Trust Comes from Evidence, Not Claims

    Reliable supply and trustworthy quality form the core of successful manufacturing relationships. That trust arises from traceable, repeatable data—every delivery of 2,5-dichlorothiophene comes with a full panel of chemical analysis, trace impurity levels, and stability data. Yet experience matters just as much. Our team has witnessed the stress that comes when a product fails to meet specs or a deadline is threatened by off-spec reagent. We remain open about our capabilities, limitations, and what actually works in the field, because the only way to build lasting partnerships is through candor and a shared commitment to practical solutions.

    Looking Ahead: Building for Sustainability and Compliance

    Our commitment extends beyond current product lines and markets. Looking forward, we’re investing in greener alternatives for core reagents, exploring lower-impact chlorination techniques that further shrink emissions. We participate in industry groups to stay current on regulatory changes—especially around substances that may fall under restriction or phase-out. Our compliance team reviews every export and shipment against global frameworks, so the product you receive meets both technical and legal standards.

    We believe open communication with end-users, regulators, and the public will define the next era of chemical manufacturing. Our experience has taught us that adaptability ensures resilience. As requirements shift—whether due to new applications or stricter regulatory frameworks—we will continue to refine and innovate around the production and delivery of 2,5-dichlorothiophene.

    Lasting Value: A Manufacturer’s Perspective

    Procurement professionals, R&D chemists, and plant managers all want transparency, responsive communication, and a product that works batch after batch. Making 2,5-dichlorothiophene at scale taught us more than just process control. Every success or snag revealed something about the value of direct technical support and honesty in business. We treat each customer’s inquiry as an opportunity to share practical know-how—not just sell a drum, but offer input that saves time, money, and headaches down the road.

    Our view remains the same: manufacturing should deliver confidence, not just product. Every lot of 2,5-dichlorothiophene leaving our plant bears the mark of this principle—crafted with care from synthesis to shipping, supported by data, refined by experience, and always ready to meet new challenges as chemistry itself evolves.