3-Bromo-2-chloropyridine-5-sulphonyl chloride

    • Product Name: 3-Bromo-2-chloropyridine-5-sulphonyl chloride
    • Chemical Name (IUPAC): 5-bromo-4-chloropyridine-3-sulfonyl chloride
    • CAS No.: 936940-79-1
    • Chemical Formula: C5H2BrCl2NO2S
    • Form/Physical State: Solid
    • Factroy Site: No.968 Jiangshan Rd., Nantong ETDZ, Jiangsu, China
    • Price Inquiry: sales7@boxa-chem.com
    • Manufacturer: Nantong Acetic Acid Chemical Co., Ltd.
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    Specifications

    HS Code

    600568

    Chemical Name 3-Bromo-2-chloropyridine-5-sulphonyl chloride
    Cas Number 720720-96-3
    Molecular Formula C5H2BrCl2NO2S
    Molecular Weight 292.96 g/mol
    Appearance White to light yellow solid
    Purity Typically ≥ 98%
    Solubility Soluble in organic solvents such as dichloromethane
    Storage Conditions Store in a cool, dry place and keep container tightly closed
    Synonyms 5-Sulfonyl chloride-3-bromo-2-chloropyridine
    Smiles C1=C(C=NC(=C1Br)Cl)S(=O)(=O)Cl

    As an accredited 3-Bromo-2-chloropyridine-5-sulphonyl chloride factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Brown glass bottle containing 25 grams of 3-Bromo-2-chloropyridine-5-sulphonyl chloride, sealed, labeled with hazard warnings and handling instructions.
    Container Loading (20′ FCL) 3-Bromo-2-chloropyridine-5-sulphonyl chloride is securely packed in sealed drums, loaded into a 20′ FCL for safe transport.
    Shipping 3-Bromo-2-chloropyridine-5-sulphonyl chloride is shipped in tightly sealed, chemical-resistant containers under cool, dry conditions. Transport complies with international regulations for hazardous chemicals, ensuring protection against moisture and physical damage. Appropriate hazard labeling and documentation accompany each shipment to ensure safe handling and regulatory compliance throughout transit.
    Storage 3-Bromo-2-chloropyridine-5-sulphonyl chloride should be stored in a cool, dry, well-ventilated area, away from moisture, heat, and incompatible substances such as strong bases and oxidizers. Keep container tightly closed and protected from light. Store under inert atmosphere if possible. Handle with care, using appropriate personal protective equipment, to prevent exposure to fumes and accidental contact.
    Shelf Life 3-Bromo-2-chloropyridine-5-sulphonyl chloride should be stored cool and dry; shelf life is typically 2–3 years in sealed containers.
    Application of 3-Bromo-2-chloropyridine-5-sulphonyl chloride

    Purity 98%: 3-Bromo-2-chloropyridine-5-sulphonyl chloride with a purity of 98% is used in pharmaceutical intermediate synthesis, where high-purity enables efficient target compound formation.

    Molecular weight 288.45 g/mol: 3-Bromo-2-chloropyridine-5-sulphonyl chloride with a molecular weight of 288.45 g/mol is used in agrochemical research, where precise molecular properties facilitate consistent reaction scaling.

    Melting point 120°C: 3-Bromo-2-chloropyridine-5-sulphonyl chloride with a melting point of 120°C is used in fine chemical manufacturing, where excellent thermal stability enhances process control.

    Particle size <10 μm: 3-Bromo-2-chloropyridine-5-sulphonyl chloride with particle size below 10 μm is used in catalyst formulation, where fine dispersion increases surface area for improved catalytic efficiency.

    Solubility in organic solvents: 3-Bromo-2-chloropyridine-5-sulphonyl chloride soluble in organic solvents is used in dye synthesis, where superior solubility ensures homogeneous reaction mixtures.

    Moisture content <0.5%: 3-Bromo-2-chloropyridine-5-sulphonyl chloride with a moisture content below 0.5% is used in heterocyclic compound production, where low moisture minimizes side reactions for higher purity yields.

    Stability at 25°C: 3-Bromo-2-chloropyridine-5-sulphonyl chloride stable at 25°C is used in reagent stock solutions, where storage stability prolongs shelf life and maintains reactivity.

    High reactivity: 3-Bromo-2-chloropyridine-5-sulphonyl chloride demonstrating high reactivity is used in sulfonamide synthesis, where rapid reaction kinetics lead to reduced production time.

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    Certification & Compliance
    More Introduction

    Introducing 3-Bromo-2-chloropyridine-5-sulphonyl chloride: A Thoughtful Approach to Specialty Chemical Manufacturing

    Bringing a new specialty chemical to market always invites a fresh look at both the science and the storytelling behind it. Our experience producing 3-Bromo-2-chloropyridine-5-sulphonyl chloride (Model: 1032906-87-4) lets us approach this compound with a perspective built from years spent in practical process development, supply chain problem-solving, and day-in, day-out batch production. This molecule may look, at first glance, like just another entry in the pyridine derivatives family. In reality, those who have worked in the synthesis of pharmaceutical intermediates and agrochemical compounds recognize its unique value the moment they see its structure.

    The Heart of 3-Bromo-2-chloropyridine-5-sulphonyl chloride

    The synthesis of 3-Bromo-2-chloropyridine-5-sulphonyl chloride didn’t arrive overnight. Our R&D teams, equipped with years of benchwork and scale-up experience, focused on producing a product with high chemical stability and repeatable batch quality. In our plant, the process begins with carefully selected feedstocks, sourced based on established supplier relationships and a deep understanding of their purity profiles. Every batch gets scrutinized by our quality control chemists who have seen the opportunities—and pitfalls—of sulphonyl chlorides.

    This compound combines three major reactive sites: a bromine at the 3-position, a chlorine at the 2-position, and a sulphonyl chloride functional group at the 5-position on the pyridine ring. Each of these groups brings unique reactivity to the table. In pharmaceutical chemistry, you see this molecule used in situations where selective transformations improve yields and shorten synthetic routes, cutting down both time and waste. The structure supports a variety of cross-coupling and nucleophilic substitution reactions. It remains particularly useful when you aim for sulphonamide libraries, or need a robust intermediate that stands up to pressure and heat better than many related derivatives.

    Our Experience with Handling and Production

    Day-to-day manufacturing of specialty halogenated pyridine derivatives tests a facility’s ability to manage stringent environmental controls and unforgiving reagents. At our plant, our production team has built up a toolbox of best practices for handling sulphonyl chlorides. Both staff training and equipment selection matter here. Maintaining anhydrous conditions shields the sensitive sulphonyl chloride group from unwanted hydrolysis, which otherwise leads to unmanageable impurity spikes. On the topic of purity, our internal standards call for HPLC purities above 98%. For those unfamiliar, anything less results in headaches downstream during pharmaceutical development or crop protection synthesis—and that’s a headache we like to avoid.

    Experience shows the value of batch consistency. Each reaction run gets tracked back to full lot traceability. Our staff have learned, through years of procedural adaptation and root-cause analysis, the subtle shifts in color and viscosity that hint at process drift or a minor deviation in raw material quality. Catching a trace impurity at this early stage has saved countless projects. We don’t talk about quality assurance as an abstract concept. Our equipment operators and lab managers recognize the fine details because they see the real impact of consistency, both in our lab analytics and in client outcomes.

    Meeting Customer Needs through Application Knowledge

    Chemists come to us looking beyond a catalog entry. The need often revolves around needing a sulphonyl chloride with a distinct halogenation pattern. Generic 2-chloropyridines or 3-bromopyridines won’t substitute for the combined chemical leverage provided by both halogen atoms in this compound, especially on a pyridine backbone. Our technical discussions with customers usually point toward its role as a key intermediate in sulphonamide synthesis. For example, pairing with amines produces target molecules that find their way into everything from anti-infectives to herbicidal agents. Sometimes, a client faces stalling at a cross-coupling step during scale-up. Our feedback, grounded in hands-on batch troubleshooting, often focuses on fine-tuning parameters for better selectivity and less byproduct formation.

    We don’t consider this product a drop-in for just any sulphonyl chloride project. The chloride at the 2-position plays a crucial role in the reactivity profile. During route scouting and process optimization, this subtle difference shapes the performance of the molecule in cross-coupling, nucleophilic aromatic substitution, or direct sulphonation routes. Some customers see better yields or higher selectivity against isomeric byproducts compared to more basic pyridine-based sulphonyl chlorides. The bromine also opens the door to Suzuki, Stille, and other coupling strategies. We’ve seen this flexibility speed up synthesis pathways for libraries of drug candidates or analogs, especially where downstream functionalization gets tricky with less versatile compounds.

    Differences from Other Pyridine Sulphonyl Chlorides

    Industry veterans will recognize a range of sulphonyl chlorides with similar-sounding names but quite different behaviors in the reactor. Take something as simple as 2-chloropyridine-5-sulphonyl chloride. That product lacks the additional bromine at the 3-position, limiting the blend of reactivity for cross-coupling applications. What this means in practical terms is fewer options for direct modification once the core scaffold is assembled.

    Similarly, compared to unsubstituted pyridine sulphonyl chlorides, our product shows greater resistance to oxidative degradation in multi-step syntheses. That stability comes from both halogenation and the electronics of the substituted ring. Chemists tell us about improved shelf-life for both the raw material and its analogues, especially when prepping multigram quantities for clinical validation runs or pilot trials.

    We have had pharmaceutical researchers report more reliable results in both sulphonamide and urea synthesis, with less waste generation and fewer purification challenges. Such feedback loops shape our own improvements, from moisture-controlled packaging to minimized batch cycle variation. The conversation with engaged chemists helps us keep both product characterization and analytical documentation up-to-date, which pays dividends during regulatory filing or patent application exercises—things we have helped customers navigate repeatedly.

    Specification and Analytical Results

    Real-world chemical manufacturing teaches respect for detailed data. That’s why every batch comes with a full certificate of analysis, including NMR, IR, and HPLC results—generated from our lab, using validated methods reviewed by both internal and external stakeholders. For most batches, we control water content to trace levels and monitor organosulphur impurities at parts-per-million. Packing is typically conducted under inert atmosphere using protective liners to guard against degradation batch-to-batch and throughout shipment.

    One misconception that sometimes arises: customers assume these handling precautions are only for regulatory appearances. In reality, it’s our own experience with temperature excursions, transit delays, or container failures that led us to adopt higher packaging standards for sulphonyl chlorides across the board. Every kilogram we deliver passed a set of hands that understands both the chemical liabilities and the demands of the end user.

    Choosing a Manufacturer for Custom Applications

    Time and again, we meet formulators, process chemists, and research directors looking for more than a generic chemical supply. Early conversations often move from specification details toward production methodologies and impurity control. A trader—or even some distributors—rarely speak to fate of trace halide byproducts formed during scale-up. Only those closely involved in batch production and kilo-to-multimodule scale-ups appreciate how a subtle process drift can change a project’s trajectory.

    3-Bromo-2-chloropyridine-5-sulphonyl chloride presents several unique opportunities for end users. For one, its distinct halogen placement strengthens its performance in custom synthesis. Pharmas using highly functionalized sulphonamides report time and material saves downstream, with less labor lost on column chromatography or costly fractional distillations. Our internal scale-up teams regularly advise on solvent systems and quench techniques that minimize byproduct formation during critical conversions.

    Sustainability and Responsible Manufacturing

    The days where specialty chemical plants treated waste management as an afterthought are long gone, and regulations rightfully caught up. Manufacturing sulphonyl chlorides requires a focus on both safe reagent handling and effective capture systems for released gases and spent solvents. We invested in process intensification and in-line monitoring to minimize emissions at every stage. Waste streams from 3-Bromo-2-chloropyridine-5-sulphonyl chloride go through our multi-stage treatment system, reducing halogen and sulphur discharge to levels that hold up under audit and contribute toward our environmental footprint targets.

    Lessons from a decade of process audits and local inspections have shaped how we monitor and report on everything from staff exposure limits to thermal stabilization. In addition, we prioritize staff training not just as a compliance measure but as a matter of operational pride. We see stronger process safety engagement and fewer lost-time incidents as a direct result.

    Challenges and Practical Solutions in Production

    Every batch of 3-Bromo-2-chloropyridine-5-sulphonyl chloride forces a manufacturer to balance efficiency with safety. While large-scale handling of sulphonyl chlorides involves tangible process risks, our operators apply lessons learned from thousands of kilograms handled over the years. Maintaining the correct temperature gradients during chlorosulphonation matters as much to final product yield as it does to personal safety. Our approach includes real-time thermal imaging, run-by-run trending, and quick intervention protocols in case of any process deviation.

    Raw material variability often challenges chemical manufacturers. Those in the business long enough know that relying on a single feedstock supplier, even a trusted one, courts trouble. We introduced multi-sourcing years ago and routinely rotate between qualified lots, cross-validated against historic retention samples, so that fluctuations in reactant quality never become a customer-facing issue.

    Packaging the finished compound seems simple on paper. In reality, external factors such as humidity surge or transport shock can initiate low-level decomposition or impurity formation, especially for a sulphonyl chloride. Our logistics and packaging teams built up solutions rooted in monitoring warehouse conditions, using compatible liners, and batch-coding each drum for backward traceability in the event of a transit claim. Each improvement arose from direct experiences, not generic guidelines.

    Open Dialogue and Continuous Improvement

    We firmly believe that success in specialty chemical manufacturing comes from open, practical communication with customers. No one questions a batch result more than a scientist working on the next-generation pharmaceutical or high-value crop protection agent. We welcome discussion about impurity profiles, help interpret analytical data, and provide feedback on compatibilities with custom synthetic pathways. Many clients circle back after months or years with new questions or updated requirements, and we see this as a signal that trust exists.

    Working closely with innovators in both established and startup research environments, we hear firsthand what drives frustration in chemical sourcing: inconsistent quality, slow response on documentation, or shipment issues at the last mile. We treat each as a solvable, concrete task—a cumulative process, not an obstacle. The product integrity remains our central focus, so there's no room for complacency around test methods or quality communications.

    Regulatory Engagement without Shortcutting Safety

    Complex molecules destined for regulated applications—especially those touching human health or food systems—face a gauntlet of compliance checks, from preclinical documentation to commercial-scale validation. Our regulatory support team takes every inquiry as an opportunity to keep our analytical and documentation standards current with global practices. Based on years of submissions for both small-molecule APIs and agrochemical actives, we built up robust internal reference standards and analytical archives. Supporting customer filings with thorough spectral libraries, impurity maps, and batch traceability isn’t just policy—it’s lived practice.

    During process audits, both independent and customer-conducted, our track record staying ahead of documentation and regulatory shifts makes a difference. Positive audit outcomes stem from a blend of technical expertise, consistent methodology, and willingness to provide data access well beyond the baseline standard. Our staff trains with the perspective that compliance doesn’t rest at meeting the letter of the law; it’s about anticipating the level of detail and reproducibility required to satisfy future market and regulatory needs.

    Looking Ahead: Supporting Next-Generation Chemical Innovation

    Every successful specialty intermediate opens doors to new molecular architectures and more efficient synthetic routes. 3-Bromo-2-chloropyridine-5-sulphonyl chloride, with its versatile halogenation and stable sulphonyl chloride moiety, lets chemists imagine a broader range of compounds with fewer synthetic detours. By reducing process steps or enabling site-specific modifications, it frees up both resources and creative time for scientists—whether in pharmaceutical labs or crop protection development.

    Feedback from end users sometimes highlights opportunities for customizations—adjusting particle size or adapting to novel solvent systems, for example. Our small pilot line remains available for collaborative process development, where tweaks at kilogram or even smaller scale pave the way for smoother tech transfer and faster product launches.

    In the broader picture, making chemicals for tomorrow’s medicines and technologies means learning from every metric: on-time delivery rates, customer complaints, cross-batch analytics, and even the handful of times a packaging redesign ended up saving a shipment during a customs inspection. Sharing those lessons keeps us grounded—and keeps each round of development sharper, whether the goal is higher purity, tighter batch specs, or innovation at the molecular level.

    Summary

    3-Bromo-2-chloropyridine-5-sulphonyl chloride reflects the real-world value of specialty chemical manufacturing—where the process, the people, and the product intertwine in practical, tangible ways. Its unique reactivity, robust stability, and tailored analytical control have enabled many research and production successes for our clients. Each improvement in its manufacturing or handling stems from facing practical challenges head-on, guided by experience and shaped by open dialogue with scientists and industry partners. From initial synthesis to final delivery, every effort reflects our commitment to quality, reliability, and the advancement of chemical science.