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5-Bromothiophenesulfonyl Chloride

    • Product Name 5-Bromothiophenesulfonyl Chloride
    • Alias 5-Bromo-2-thiophenesulfonyl chloride
    • Einecs 413-070-1
    • 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

    690123

    Cas Number 703-94-8
    Molecular Formula C4H2BrClO2S2
    Molecular Weight 261.55 g/mol
    Appearance White to light yellow solid
    Melting Point 56-58 °C
    Purity Typically ≥ 98%
    Storage Conditions Store in a cool, dry place; keep container tightly closed
    Solubility Reacts with water; soluble in organic solvents (e.g., dichloromethane)
    Synonyms 5-bromo-2-thiophenesulfonyl chloride
    Smiles C1=C(SC=C1Br)S(=O)(=O)Cl
    Inchikey XGVHDVXYGSSLPC-UHFFFAOYSA-N
    Hazard Statements Corrosive; causes burns, irritating to eyes, respiratory system and skin

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

    Packing & Storage
    Packing 5-Bromothiophenesulfonyl Chloride, 10g: Supplied in a sealed amber glass bottle with tamper-evident cap, labeled with hazard information.
    Shipping 5-Bromothiophenesulfonyl chloride is shipped in secure, airtight containers to prevent moisture and contamination. Transported as a hazardous material, it is clearly labeled and handled according to regulatory guidelines. The chemical is stored in cool, dry conditions and protected from light, with safety data sheets included in the shipment documentation.
    Storage 5-Bromothiophenesulfonyl chloride should be stored in a cool, dry, and well-ventilated area, away from moisture, heat, and incompatible substances such as bases and strong oxidizers. Keep the container tightly closed and protected from light. Store under inert gas, such as nitrogen or argon, if possible. Handle with proper personal protective equipment to avoid contact with skin and eyes.
    Application of 5-Bromothiophenesulfonyl Chloride

    Applications of 5-Bromothiophenesulfonyl Chloride in Industrial Manufacturing

    5-Bromothiophenesulfonyl Chloride is an essential intermediate in several high-value chemical synthesis processes. Our direct manufacturing experience enables us to support large-volume and specialty applications for active pharmaceutical ingredient (API) synthesis, advanced agrochemical intermediates, OLED material building blocks, and specialty polymer additives. Each of the following sectors employs distinct formulation guidelines, compliance standards, and production methodologies, reflecting the critical role of this raw material in precise downstream processes.

    1. Pharmaceutical API Intermediate Synthesis

    Pharmaceutical innovators use this intermediate in targeted sulfonylation and bromination steps of small-molecule synthesis, particularly within certain anti-infective and cardiovascular drug classes. Rigorous documentation and validated process controls align with GMP requirements, as downstream partners demand both traceability and reaction reproducibility for late-stage intermediates destined for regulated markets.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP General Chapters <791> & <1092> for chemical purity and reference standards
    • EU GMP Annex 8 for raw material supply chain traceability
    • 21 CFR Part 211 for finished pharmaceutical controls

    Typical usage ratio

    • Applied at 0.85–1.20 molar equivalents relative to the target nucleophilic aromatic substrate; specific ratio adjusted according to route yield and desired byproduct control.

    Downstream process integration

    • Charged to a jacketed glass-lined reactor under dry nitrogen during sulfonyl chloride introduction; reacts at low temperatures with amines or phenols to produce advanced intermediates for further functionalization.

    Final product types

    • Advanced pharmaceutical intermediates for anti-bacterial, anti-hypertensive, or CNS-active APIs
    • Drug substance building blocks requiring high sulfonylation fidelity

    2. Agrochemical Intermediate Synthesis

    Leading agrochemical companies use the compound as a reactive sulfonylating agent, introducing bromothiophene motifs into herbicide and fungicide precursor structures. The manufacturing protocols emphasize operator safety, scalable reaction control, and compliance with pesticide precursor regulations, reflecting the stringent downstream validation by multinational crop protection formulators.

    Industry compliance standards

    • ISO 9001:2015 Quality Management System
    • FAO/WHO Specifications for Pesticide Active Ingredients
    • REACH Regulation (EC) No 1907/2006 for intermediates
    • Good Laboratory Practice (GLP) for analytical verification

    Typical usage ratio

    • Usually added at 0.95–1.10 molar equivalents to aromatic core acceptor compounds; precise loading managed to restrict unreacted sulfonyl chloride carry-over.

    Downstream process integration

    • Metered directly into the reaction vessel after initial solvent charging; sulfonyl chloride moiety activates heterocyclic rings before further alkylation, halogenation, or cyclization steps in protected production environments.

    Final product types

    • Precursor intermediates for sulfonylurea herbicides
    • Key sulfonylated compounds for selective fungicide synthesis

    3. OLED and Organic Electronic Material Synthesis

    Advanced material researchers employ this compound as a functionalization agent for fine-tuning charge transport properties in the synthesis of small-molecule and polymer semiconductors for displays and lighting. Compliance with electronics-industry raw material assessment focuses on trace metal content and batch-to-batch reproducibility for efficient downstream polymerization or cross-coupling reactions.

    Industry compliance standards

    • RoHS Directive 2011/65/EU for restriction of hazardous substances
    • ISO 14644-1 Controlled Environment (where applicable)
    • OEM-specific raw material purity and contamination thresholds
    • IEC 61249-2-21 for halogen content

    Typical usage ratio

    • Employed at 1.00–1.05 equivalents in aryl-sulfonation steps; slight excess applied only when downstream purification allows, to maximize yield.

    Downstream process integration

    • Dosed during key monomer or oligomer modification stages, often in anhydrous, controlled-atmosphere environments; participates in Pd- or Cu-catalyzed cross-coupling for marrying functionalized thiophenes onto polymer or small-molecule frameworks.

    Final product types

    • Thiophene-based monomers for OLED emitting layers
    • Functionalized building blocks for hole/electron transport materials

    4. Specialty Polymer Modifier Synthesis

    Producers of high-performance specialty polymers use this compound to introduce reactive sulfonyl-bromothiophene units into customized macromolecular chains, enhancing selectivity and stability in demanding end-use environments. Compliance with downstream polymer GMP and specific resin quality standards is critical, as downstream QC must demonstrate consistent incorporation and end-group structure.

    Industry compliance standards

    • ISO 9001:2015 Quality Management System
    • ASTM D6286 for polymer composition traceability
    • Customer-specific technical and analytical agreement protocols
    • Polymer industry environmental, health, and safety (EHS) audit requirements

    Typical usage ratio

    • Typically 2–8 wt% relative to total monomer feed in copolymerization reactions; adjusted based on targeted degree of sulfonation and required mechanical or electrical properties in the final polymer.

    Downstream process integration

    • Fed continuously or batchwise into a co- or terpolymerization reactor with other aromatic and heterocycle monomers; compatible with solution, emulsion, and bulk polymerization techniques demanding moisture-free solids handling.

    Final product types

    • Engineered specialty resins for membrane separation
    • Functional copolymers and ionomers with enhanced chemical durability
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    Certification & Compliance
    More Introduction

    5-Bromothiophenesulfonyl Chloride: Finding Clarity in Specialty Organosulfur Chemistry

    Stepping Up to Today’s Lab Challenges

    The demand for specialty intermediates never slows in our business. Over the last decade, researchers and process engineers continue to raise the bar on molecular complexity, asking for building blocks that can do more than just fill a reaction space—products that genuinely enable progress. We have seen 5-Bromothiophenesulfonyl Chloride play a critical role in these conversations. Those who work hands-on with synthetic routes know its value in cross-coupling, pharmaceutical assembly, and agrochemical development. We make this compound for people solving complex synthetic puzzles, not for catalog shelves or speculative trade.

    What Makes 5-Bromothiophenesulfonyl Chloride Stand Out?

    In our shop, we focus on quality. Each batch of 5-Bromothiophenesulfonyl Chloride leaves our line because it meets demanding analytical standards. Years of process refinement have tuned our output to produce a product with strong batch-to-batch consistency. Researchers working with tight structure-activity relationships consistently tell us that inconsistent reactivity derails their projects. Rigorous NMR, GC, and titration protocols spot any sign of side-reactions or variable sulfur content; a clean, pale solid with a reliable melting point means researchers know their electrophile will perform as intended, and downstream purification steps won’t become bottlenecks.

    Technical staff investigating new heterocycle core areas repeatedly stress the need for robust, pure sulfonyl chlorides. In our own early process trials, side products from incomplete bromination or thiophene overreaction triggered frustration for weeks. Moving away from bulk commodity thinking, we saw that over-crystallization could lock in trace impurities no matter how pure the feedstock. Refining filtration times, solvent mixtures, and temperature ramps made all the difference. Years of fine-tuning let us dial in to the reliable, workable specs that industry labs actually rely on—every order, every kilo.

    Manufacturing with Purpose

    Our approach pivots around control and reliability. Bringing a brominated thiophenesulfonyl structure into a process isn’t about chasing purity for purity’s sake, but about letting downstream chemistry run without drama. Synthetic chemists often have very little patience for batch hiccups—if a batch doesn’t match spec, it delays the entire program. Our team responds quickly when queries arise because every new observation can drive a more robust, more thoughtful process.

    Experience shows that robust handling of volatile and reactive sulfur-chlorine reagents matters more than perfecting one step in isolation. In the real world, excess sulfonyl chloride or trace hydrolysis leads to nagging corrosion, yield dips, or byproduct headaches. Strict glovebox loading no longer fits the efficiency needs of today’s research labs or pilot plants. We realized this early and designed our process to allow for practical, benchtop-level handling without artistic glass blowing or weekly filter rebuilds. With this focus, more labs have been able to move from milligram discovery to multi-gram and beyond without rewriting protocols or needing custom safety gear.

    We understand this because we’ve run the same hurdles. Our own pilot projects required us to swap out glassware more than once after a bad batch, prompting a revamp of our storage and containment practices. This direct experience feeds every update we push into our batch handling, drumming, and transport. Our technical team comes from chemistry, not marketing, so the lessons stick.

    What Sets It Apart from the Crowd?

    Structurally, 5-Bromothiophenesulfonyl Chloride offers an unusual blend of functionalities—sulfonyl chloride reactivity plus the utility of a protected bromo position. Thiophene rings have built a reputation for stable aromaticity mixed with ease of substitution. You don’t often see easy access to mixed sulfonyl-bromo-thiophene cores. We’ve seen projects in both pharmaceuticals and materials science take advantage of this: medicinal chemists want the option to couple or swap the bromine site selectively, while others exploit the sulfur group for attachment or further derivatization.

    Several years ago, an API client needed better reactivity at the bromo position for Pd-catalyzed couplings, but off-the-shelf sulfonyl chlorides kept producing inconsistent yields and unknown side-products. Direct feedback showed that minor impurities or moisture carryover in some other sources blocked the coupling step or forced extensive cleanup. Our in-house runs, tightly monitored for water and residual acid, let them solve a scale-up bottleneck. Once we closed the gap and maintained tight controls, analytical reproducibility improved—and so did their project’s timelines. Stories like this give us confidence in the process and the compound’s unique place in our lineup.

    Compared to unsubstituted thiophenesulfonyl chloride or to para-chlorinated analogs, the 5-bromo group adds enough electronic withdrawal to drive selectivity without losing stability. The reactivity profile brings a balance: reactive enough for nucleophilic aromatic substitution, tolerant of diverse coupling partners, still bench-stable in proper dry storage. Prime competitors often target only the bulk trade at the expense of grade variance. We believe a strong relationship with active users shapes our product’s edge; this is a compound designed around real-world synthesis, not theoretical idealism.

    Enabling Coupling Chemistry and Beyond

    A significant chunk of research demand for 5-Bromothiophenesulfonyl Chloride comes from those exploring cross-coupling chemistry. Traditional aryl bromides make reliable partners for Suzuki, Stille, and Buchwald-Hartwig couplings, and our product finds a natural home here. The added sulfonyl chloride offers new handles for further derivatization or for sulfonamide bond formation. Labs investigating novel kinase inhibitors or electronic materials often need to stitch together scaffolds where each bond-forming step depends on the underlying quality of the partner. We tune our product so its purity and reactivity match these sensitive, high-stakes applications.

    Pharmaceutical discovery platforms today utilize a palette of diverse chemical handles but push them to small scale before larger needs emerge. We’ve worked closely with clients who started with gram-scale exploratory chemistry and needed smooth, scalable access to precision intermediates as soon as success hit. The ability to deliver homogeneous, reproducible material, batch after batch—not just the initial pilot lot—sets us apart. We monitor metrics like acid chloride content, residual bromide, and water load every time. Large-scale blending or “cutting” is never a way to solve a problem here; we dig for the cleanest source at every step, even when raw material prices or regulatory conditions shift.

    Fine chemical users repeatedly point out that seemingly minor issues—color drift, inconsistent particle sizing, or trace polymerization—lead to major headaches in HPLC, flash column, or solid-state handling. We tackle this with adjustments in drying cycles and with mechanical sieving, not with sweeping product specs under the rug. Good chemistry support always begins with a supplier who’s been through the same pain. We don’t build vague “one size fits all” solutions, but listen to the needs driving actual synthesis design.

    Safe, Reliable Handling Recommendations Built on Real Experience

    Those who work with thionyl-based and sulfonyl-based chlorides day in and day out develop a healthy respect for moisture sensitivity and the volatility of acid chlorides. 5-Bromothiophenesulfonyl Chloride is no different. Our team implements drying, packing, and quality-release protocols that don’t over-engineer or under-prepare. Engineers have optimized temperature ramps during drying and loading, and we handle all product in environments where relative humidity remains strictly controlled. Direct transfer to air-tight, inert-gas sealed drums or liners keeps product fresh and stable during storage and transit.

    Over the years, we’ve come across labs running routine prep without access to specialist dryers or complex containment. Sharing processing tips, such as minimizing headspace in storage vials and using desiccant packs during bench work, speeds up project onboarding. No level of documentation replaces candid conversation between those making the product and those using it in the fume hood. Teams tell us they can spot the difference—a product made by those who care about real-world outcomes, not just the numbers in a spec sheet.

    Recognizing and Addressing the Real Issues

    One truth we learned early: material cost and reliability mean little if the consistency isn’t there. Earlier in our manufacturing journey, we saw a number of incoming projects stall or even fail due to variability from bulk intermediates, usually sourced from generic commodity brokers lacking specialty focus. Every time a client called to troubleshoot a downstream failure—and it often turned out to be down to trace instability, not a broken protocol—it reinforced our drive to invest in better batch testing and operator training.

    Without direct experience in scale-up and kilo-lab environments, it’s easy for a supplier to overlook the practical details: minor pH drift, residual solvent, invisible mechanical fines. Our team works hands-on in both development labs and production lines, so the learning flows both ways. When we changed our internal process to cut out a common solvent residue, HPLC traces from collaborators improved enough to save entire days of cleanup. The savings in work hours and frustration pay dividends on both sides.

    Looking ahead, new regulations around hazardous chemicals and transport safety reshape the supply chain for everyone. With fresh attention on data transparency and handling records, our ability to trace each lot from drum to drum stands on practical systems, not disconnected paper trails. Lab users appreciate being able to connect with actual production chemists or engineers, not handed off to generic salespeople. This keeps us sharp and ensures the product evolves alongside end-user needs.

    Comparisons with Other Synthetic Intermediates: Knowing What Works

    It’s tempting to consider pooling resources among several sulfonyl chlorides or brominated heterocycles, treating each as simple variations on a theme. Real chemistry tells a different story. 5-Bromothiophenesulfonyl Chloride triggers unique reactivity patterns; the offset electron density from both the bromo group and the sulfonyl chloride creates selectivity options that plain thiophenesulfonyl or unbrominated analogs can’t match. Multi-site activation or controlled mono-coupling becomes easier with material that’s been visibly characterized and properly stabilized.

    We’ve compared our product performance on actual reactions in unbiased settings. For example, rigorously controlled Suzuki and amide formation runs using our material tend to deliver tighter mass balances, sharper NMRs, and lower off-product formation than similar grades from bulk resellers. We do not chase the lowest cost per mole. Instead, repeat customers stick with us because reliable performance supports discovery and scale-up in oncology, CNS, and agricultural pipelines.

    Other suppliers might tout quantity or purity numbers alone. We believe in process transparency over abstract claims. That means ongoing discussions about the best way to handle reactivity, control for residual solvent, and adapt the final product to niche requirements—rather than one-off purifications or blended solutions that add subtle, but damaging, unknowns to downstream runs.

    Building the Future with Practical Experience

    Every new synthetic route presents variables and unknowns. Our bond as manufacturer to the working chemist is built on direct feedback, ongoing iteration, and lessons drawn from both successes and the missteps. 5-Bromothiophenesulfonyl Chloride occupies a valuable niche, one where bench-level reliability makes or breaks downstream efficiency. We invest in learning about actual user pain points, adjusting specs in partnership with lead chemists and process engineers rather than in isolation.

    With global supply chains under pressure and access to fine chemicals under constant scrutiny, credible documentation, stable supply agreements, and open ear to changing project aims mean more every year. The relentless grind of industrial chemistry doesn’t allow for “good enough”. Those willing to aim higher, to challenge their own process, and to share in end-user success, will always have something more meaningful to offer—today, and in the ever-evolving world of specialty organosulfur building blocks.