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4,5-Dibromothiophene-2-Sulphonyl Chloride

    • Product Name 4,5-Dibromothiophene-2-Sulphonyl Chloride
    • Alias 2-Thiophenesulfonyl chloride, 4,5-dibromo-
    • Einecs 631-198-6
    • 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
    VTB
    Specifications

    HS Code

    182656

    Product Name 4,5-Dibromothiophene-2-Sulphonyl Chloride
    Cas Number 41905-44-6
    Molecular Formula C4HBr2ClO2S2
    Molecular Weight 338.44 g/mol
    Appearance Off-white to light brown solid
    Solubility Reacts with water, soluble in organic solvents
    Purity Typically ≥ 95%
    Storage Condition Store in a cool, dry place, tightly closed
    Application Organic synthesis, especially in preparation of sulfonamide derivatives
    Hazard Statements Corrosive, causes burns, may release toxic gases on contact with water
    Smiles Brc1c(sc(c1Br)S(=O)(=O)Cl)

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

    Packing & Storage
    Packing The 25g of 4,5-Dibromothiophene-2-Sulphonyl Chloride is supplied in a sealed amber glass bottle with hazard labels.
    Shipping 4,5-Dibromothiophene-2-Sulphonyl Chloride is shipped in sealed, chemical-resistant containers under cool, dry conditions. It is classified as hazardous, requiring appropriate labeling and documentation. Transport must comply with local and international regulations, including UN numbers and safety procedures, to ensure protection against leakage, moisture, and accidental exposure during transit.
    Storage 4,5-Dibromothiophene-2-sulphonyl chloride should be stored in a tightly sealed container, away from moisture, heat, and direct sunlight. Store in a cool, dry, and well-ventilated area, separate from incompatible substances such as strong bases and water. Use secondary containment to prevent spills, and label storage areas clearly. Handle with care, using appropriate personal protective equipment.
    Application of 4,5-Dibromothiophene-2-Sulphonyl Chloride

    Applications of 4,5-Dibromothiophene-2-Sulphonyl Chloride in Industrial Manufacturing

    As an established manufacturer of 4,5-Dibromothiophene-2-sulphonyl chloride, we support specialized downstream industries requiring high-purity halogenated thiophene derivatives for synthesis and advanced materials production. The following application scenarios illustrate the industrial integration of this intermediate, grounded in current market practice and strict compliance with international standards.

    1. Pharmaceutical Intermediates for Thiophene-based API Synthesis

    Leading pharmaceutical producers utilize this compound in the targeted assembly of thiophene-containing active pharmaceutical ingredients, especially for antimicrobial and anti-inflammatory agents where brominated heterocyclic scaffolds impart critical biological properties. The material enters multi-stage synthesis routes as a sulfonyl chloride building block, ensuring regioselective substitution patterns essential in new drug candidates disclosed in contemporary drug patents.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • 21 CFR Parts 210 & 211 (U.S. FDA)
    • European Pharmacopoeia (Ph. Eur.) General Chapters for Intermediates
    • REACH Annex XVII (for chemical handling and safety)

    Typical usage ratio

    • Reactant use varies from 0.2 to 0.8 molar equivalents dependent on the stage-specific stoichiometry; precise dosage adjusted based on intended substitution degree and process yield targets.

    Downstream process integration

    • Charged as a sulfonylating and brominating agent during the late-stage assembly of heterocyclic scaffolds.
    • Introduced under controlled temperature and pH conditions for coupling reactions, followed by solvent exchange and purification.

    Final product types

    • Antibacterial pharmaceuticals with thiophene backbone
    • Anti-inflammatory drug molecules
    • Small molecule kinase inhibitors incorporating halothiophene derivatives

    2. Organic Electronic Materials: Conductive Polymer Precursor

    Electronic materials producers select this compound during the synthesis of functionalized polythiophenes used in flexible organic electronics and thin-film transistors. Its dibromo-functional group enables precise copolymerization or cross-linking, aiding in the formulation of high-purity, solution-processable conductive polymers with reliable electronic properties for use in optoelectronic devices.

    Industry compliance standards

    • RoHS Directive 2011/65/EU (Restriction of Hazardous Substances)
    • IEC 62474 Material Declaration for Products of and for the Electrotechnical Industry
    • ISO 9001:2015 Quality Management
    • Customer-specific electronic grade purity (≥99.5%)

    Typical usage ratio

    • Monomer feed concentration commonly 1.0–3.0% w/w in the polymerization mixture; actual ratio adjusted according to desired molecular weight and conductivity profile in the final polymer matrix.

    Downstream process integration

    • Introduced during monomer charging to enable step-growth or chain-growth polymerizations.
    • Followed by in situ oxidative polymerization and doping, then film casting and annealing steps.

    Final product types

    • Polythiophene conductive inks
    • Organic field-effect transistor (OFET) backplanes
    • Transparent electrode films for touchscreens and flexible displays

    3. Agrochemical Active Ingredient Synthesis

    Leading crop protection formulators employ this material as a key intermediate in the multi-step synthesis of thiophene-based fungicides, particularly when the molecular structure demands precise bromination patterns and sulfonyl chloride reactivity for linkage formation. It supports tailored heterocycle construction, contributing to the activity spectrum and stability of modern agrochemical actives.

    Industry compliance standards

    • FAO/WHO JMPR Guidelines for pesticide residues
    • ISO 17025 Testing and Calibration Laboratories
    • Directive 2009/128/EC (EU Sustainable Use of Pesticides)
    • China Pesticide Registration Regulation (GB 4839-2020)

    Typical usage ratio

    • 0.25–1.2 mole equivalents per batch, set according to conversion targets in the sulfonamide or heterocycle coupling step; optimization depends on route and side-product minimization.

    Downstream process integration

    • Bathed into the coupling reaction with nitrogen nucleophiles, then isolated via extraction and crystallization.
    • Pre-final purification after the main synthetic stage before formulation into active ingredient concentrate.

    Final product types

    • Systemic fungicide active ingredients
    • Precursor to crop protection molecular scaffolds with thiophene core
    • Intermediate for combination pesticide synthesis

    4. Specialty Dye and Photosensitizer Manufacturing

    Advanced dye and pigment makers incorporate this sulfonyl chloride in the multi-step assembly of organic chromophores for specialty textile, photographic, and LED applications. The unique combination of sulphonyl chloride and dibromo substitution allows for tailored molecule design, enabling processers to engineer dyes with customized light absorption, color fastness, and stability characteristics.

    Industry compliance standards

    • OEKO-TEX Eco Passport for chemical inputs
    • ISO 105-A02: Color Fastness to Washing
    • ISO 14001 Environmental Management
    • REACH Regulation (EC) No 1907/2006 – SVHC Disclosure

    Typical usage ratio

    • Blending levels in organic synthesis formulations typically 0.5–2.0 equivalents per coupling or condensation stage; tuning based on target dye shade and photoactive behavior.

    Downstream process integration

    • Fed into aromatic substitution and sulfonamide-forming stages of chromophore synthesis.
    • Subsequent purification by liquid-liquid extraction and column chromatography.

    Final product types

    • Organic dyes for technical textiles
    • Photosensitizers for dye-sensitized solar cells (DSSC)
    • Specialty pigments for LED phosphors and imaging technologies
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    Certification & Compliance
    More Introduction

    4,5-Dibromothiophene-2-Sulphonyl Chloride: A Practical Perspective from Our Factory Floor

    As a chemical manufacturer dedicated to real-world needs and valued partners in research and industry, we have worked daily with 4,5-dibromothiophene-2-sulphonyl chloride—often simply known among our team by its batch code, because in the plant, chemistry gets personal. Every pallet we produce stands as proof of our hands-on knowledge, not just formulas in a catalog.

    Understanding 4,5-Dibromothiophene-2-Sulphonyl Chloride

    4,5-Dibromothiophene-2-sulphonyl chloride carries a mouthful of a name, but its purpose in advanced organic synthesis stays clear to those of us who make it. Chemists see it as a valuable intermediate for sulfonylation reactions. Our reactors charged their first run of this compound more than fifteen years ago, when demand for new methods in aryl sulfonylation took a leap.

    The structure features two bromine atoms at the 4 and 5 positions on the thiophene ring, alongside a reactive sulfonyl chloride group at position 2. This backbone matters for one reason—reliable reactivity. In our experience, this arrangement has turned 4,5-dibromothiophene-2-sulphonyl chloride from a niche curiosity into a mainstay of research labs and specialty chemical plants with serious needs for precision building blocks.

    From Synthesis to Purification: Our Process in Detail

    We know pure chemistry doesn’t come easy. Each batch of 4,5-dibromothiophene-2-sulphonyl chloride running through our reactors starts with carefully sourced thiophene. Bromination steps demand strict control. Sulfonyl chloride moieties can turn volatile, so we watch temperature, pressure, and every drop passing through glassware or steel. Indoor air on production days smells sharp—proof of reactive chemistry in action.

    Once the reaction finishes, the work hardly ends. Removal of trace impurities decides the difference between a usable chemical and a problematic one. In-house purification columns, high-vacuum distillation, and targeted crystallization allow us to shape a consistent, pale yellow product—free-flowing or crystalline, depending on downstream needs. Analysis happens right on site. Our team gets immediate feedback when a fraction veers off spec, and rejects don’t leave the plant.

    Our typical specification for 4,5-dibromothiophene-2-sulphonyl chloride holds an assay well above 98% by HPLC, with moisture content below 0.5%. We run routine GC-MS and NMR checks to be sure. These numbers aren’t just for paperwork—customers who scale up sulfonylation reactions need genuine reliability in every shipment.

    Where Chemists Reach for 4,5-Dibromothiophene-2-Sulphonyl Chloride

    Big applications start with seemingly minor details. In practice, 4,5-dibromothiophene-2-sulphonyl chloride takes on a unique role as a building block in the development of advanced materials and pharmaceuticals. Where research labs design new polymers, this compound unlocks thiophene structures that would be hard to access otherwise.

    Close up, the two bromine atoms act as handles. They offer sites for Suzuki, Stille, or Negishi couplings, which helps researchers stitch together large, complex molecules step by step. The sulfonyl chloride group, in contrast, opens pathways to tailored sulfonamides, sulfonate esters, or further modified aryls.

    In real projects, chemists value how the dual reactivity of the bromine and sulfonyl groups leaves room for sequential transformations. Lab notebooks from collaborators have traced elegant routes from our product through half a dozen creative reactions, ultimately landing on new heterocyclic cores or next-generation electronic materials. What starts as a small package leaving our plant can end up shaping an OLED display, a diagnostic probe, or a fragment of a pharmaceutical lead.

    Lessons from Making and Handling This Product

    Long-term handling of 4,5-dibromothiophene-2-sulphonyl chloride teaches respect for its strengths and its hazards. Chlorinated sulfonyl groups bite back if left open to moisture—hydrolysis not only destroys the reactive functionality but can turn a whole batch into unsalable waste. Our storage drums live in climate-controlled, low-humidity conditions. Warehouse staff understand the need for quick, clean transfers, and we keep desiccant packs at hand.

    Shipping regulations classify this compound as hazardous. We double seal liners, check tightness on all closures, and do not compromise on labeling. Local partners have shared that care in logistics pays off—a delayed customs clearance or a leaky drum can set months of work back. We have revised our shipping protocols over the years based on every incident and every near-miss, with input from seasoned transport specialists.

    On the lab front, our team reviews new safety data, not just once a year, but every time the procedure changes. Spill kits, fume hoods, and neutralizers stay close to the point of use. The sharp, pungent odor warns of leaks but we don’t depend solely on our noses—online monitoring for volatile organics in sensitive zones protects every worker on shift.

    Comparing 4,5-Dibromothiophene-2-Sulphonyl Chloride to Other Chemical Intermediates

    Having seen hundreds of similar compounds move across our formulation line, the unique value of 4,5-dibromothiophene-2-sulphonyl chloride stands out. Direct competitors include mono-brominated or unsubstituted thiophene sulfonyl chlorides. These alternatives present lower reactivity profiles or less flexibility. Mono-bromo versions restrict the possible cross-coupling steps. Without the sulfonyl chloride group, thiophene bromides lose the ease of access to sulfonamide or sulfonate derivatives.

    Other paired-bromo aromatic sulfonyl chlorides (on benzene rings, for example) miss the electron-rich nature of thiophene. This feature leads to higher reactivity in electrophilic aromatic substitutions, helping chemists achieve target molecules with fewer side reactions. Customers regularly relay how the thiophene ring helps yield clean, efficient coupling, particularly for heterocycle-rich scaffolds.

    Formula weight, melting point, and solubility characteristics remain distinct as well. Compared to the lighter, unsubstituted derivatives, 4,5-dibromothiophene-2-sulphonyl chloride handles a bit heavier but dissolves efficiently in polar aprotic solvents like DCM, DMF, or THF—a trait that matters when scaling up to pilot reactors or kilo labs. Solid-state behavior remains stable for long-term storage if handled with care.

    Industry Trends and the Demand for Specialty Building Blocks

    Decades of manufacturing in the sector have revealed a steady shift toward more functionalized intermediates. Researchers want flexibility and reactivity. Off-the-shelf, mono-functional thiophenes handled many traditional synthetic jobs, but the latest material science projects demand larger, more complex backbones. Smart drug design, high-mobility polymers, and sensitive imaging probes all draw on the advantages of bifunctional or trifunctional intermediates.

    We respond by tuning our procedures and capacities year on year. No mass production shortcuts can replace the need for precise, repeatable batches. The push for greener chemistry has also led to a sharper look at waste streams and byproducts. Our process development group has cut waste chloride generation by a third in the past five years, simply by tightening the exotherm control and switching some process solvents for more recyclable options. These plant upgrades may not get headlines, but everyone on shift knows the broader impact.

    New applications have emerged from smaller research groups and major industrial partners alike. Whenever we supply a fresh lot of 4,5-dibromothiophene-2-sulphonyl chloride to a materials science group, we check in on project progress and encourage feedback that can feed future efforts. Our batch records still leave room for handwritten notes on product outcomes—those on-the-floor learnings return value many times over as we adapt scale, purity, or crystal form to support new syntheses.

    Product Reliability and Real-World Challenges

    A reliable supply of 4,5-dibromothiophene-2-sulphonyl chloride supports the productivity of hundreds of research projects worldwide. It’s easy to take consistency for granted when every bottle looks the same, but as manufacturers, we know what it takes to keep every parameter locked in tight.

    Weather disruptions, global ingredient shortages, and regulatory changes can push raw material costs up or squeeze critical supplies. We secure multi-source supply chains and keep safety stocks on hand. Once, a run of subpar thiophene from a regular supplier set our whole schedule back two weeks. That batch never left our doors. We have since expanded supplier vetting and now conduct random incoming QC analysis to keep such problems off the line.

    Every kilogram shipped comes out of the efforts of teams on the plant floor, the QA lab, and in logistics. We keep training current, cross-train staff to cover every process step, and invest in new safety protocols every budget cycle. The number of variables may be higher than chemists outside manufacturing realize, but steering through these moving pieces is a normal part of our day.

    For customers scaling up, we keep technical support available. Our production engineers and chemists know the shortcuts—and the traps—in scaling laboratory syntheses to multi-liter reactors. Batch-to-batch variation in reactivity, color, crystallinity, or solubility never escapes notice. We read all feedback, figure out root causes, and redesign processes when needed.

    Commitment to Quality and Transparent Practices

    Quality results from day-to-day discipline, not just published standards. We have seen new customer relationships pivot on a single out-of-spec assay. Every batch moves through full analytical review. HPLC, NMR, GC-MS, and visual inspections—every tool brings a different perspective, helping us spot even the minor inconsistencies that can disrupt downstream chemistry.

    Openness counts across the board. If a shipment delays or a batch falls short, we inform partners honestly. No hidden issues, no ambiguous excuses. Over years, customers have told us that this honesty keeps their schedules on track, even when it means a tough conversation. This trust, built over time, stands up far better than rigid contracts or empty reassurances.

    We realize each lot of 4,5-dibromothiophene-2-sulphonyl chloride affects more than our own bottom line. Project delays, failed syntheses, or wasted hours in the lab cost real people real progress. We hold ourselves responsible for supporting those efforts with reliable, safe, and consistently made product every time.

    Looking Forward: Challenges and Improvements Ahead

    Production standards must evolve with industry expectations. Today’s customers ask for increased documentation, traceability, and shipping flexibility, not just a high-purity product. We have digitized batch records, rolled out serialization, and steadily improved our internal IT to keep every record accurate and retrievable.

    Ongoing research hints at future products based on this same core—perhaps new substitution patterns, tailored counterions, or integrated purification steps for direct downstream use. We monitor the literature and listen closely to feedback from the research community. If a project needs grams rather than kilos, or requests a unique polymorph, we tap our pilot lab to accommodate. One collaboration currently explores scalable synthesis of a trisubstituted variant, opening another layer of synthetic versatility.

    Environmental concerns have pushed us to re-evaluate key reagents and waste-disposal routes. Our investment in waste management not only supports regulations, but also aligns with our own values for responsible chemical manufacturing. Switching to alternative chlorinating agents cut the environmental impact meaningfully. On-site waste capture and responsible off-site processing lock in further gains.

    Across all departments, staff remains key. Shifting protocols require retraining, and we maintain a hands-on system for bringing plant operators and new chemists up to speed. Our trainers work side by side with new workers for their first month in specialty manufacturing, ensuring every team member respects the subtleties of each batch. Machine monitoring and digital records support—but never replace—the experienced eyes and steady hands that daily move chemicals from shipment to package.

    Real improvements take time and steady investment. Our owners committed years ago to regular capital spending on new reactors, upgraded containment, and modern lab equipment. Each investment ripples through the plant, sharpening quality and safety. Feedback loops run from operator to engineering to sales, looping back as new orders challenge us to raise standards once again.

    Final Thoughts from Our Experience

    Making 4,5-dibromothiophene-2-sulphonyl chloride is more than moving chemicals from drum to bottle—it’s a daily exercise in problem solving and integrity. Our staff builds reliability batch by batch, conscious that every shipment reflects on both our plant and the downstream science it powers.

    While laboratory guides and supplier catalogs provide textbook descriptions, those of us who have spent years refining batches know that no two process runs are truly alike. The consistency, quality, and safety of each order depend on decisions by people: those who adjust the temperature, track the chromatography, and double-check the shipment paperwork before a truck rolls out.

    The work brings challenges. Mistakes have happened, and we have faced tight deadlines, regulatory hurdles, and raw material shortages. Each challenge has refined our processes and our outlook. The lessons learned through years of production drive every improvement, whether for purity, logistics, or customer support.

    With each batch, we commit ourselves to supporting the chemists, engineers, and researchers who depend on truly functional building blocks. As the demand for complex heterocycles and advanced functional molecules grows, 4,5-dibromothiophene-2-sulphonyl chloride stands as a testament to the value of careful manufacturing, steady investment, and transparent business relationships.

    We look forward to supplying partners both new and established, sharing in the advances made possible by reliable specialty chemistry, and improving every part of the process as experience, technology, and industry needs evolve.