Products

4-Bromobenzenesulfonyl Chloride

    • Product Name: 4-Bromobenzenesulfonyl Chloride
    • Alias: Benzenesulfonyl chloride, 4-bromo-
    • Einecs: 224-325-4
    • Mininmum Order: 1 g
    • Factroy Site: Yudu County, Ganzhou, Jiangxi, China
    • Price Inquiry: admin@ascent-chem.com
    • Manufacturer: Ascent Petrochem Holdings Co., Limited
    • CONTACT NOW
    Specifications

    HS Code

    525261

    Name 4-Bromobenzenesulfonyl chloride
    Cas Number 98-60-2
    Molecular Formula C6H4BrClO2S
    Molecular Weight 255.52 g/mol
    Appearance White to off-white crystalline powder
    Melting Point 93-96 °C
    Density 1.82 g/cm³
    Solubility Reacts with water, soluble in organic solvents like dichloromethane
    Purity >98% (typical)
    Synonyms p-Bromobenzenesulfonyl chloride, 4-Bromo-benzenesulfonyl chloride
    Storage Conditions Store in a cool, dry place, tightly closed container, under inert atmosphere

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

    Packing & Storage
    Packing 4-Bromobenzenesulfonyl chloride, 25g, packaged in a sealed amber glass bottle with a secure screw cap for moisture protection.
    Shipping 4-Bromobenzenesulfonyl chloride is shipped in tightly sealed containers, protected from moisture and light. It is classified as a hazardous material, requiring compliant packaging and labeling according to international transport regulations. Proper documentation, temperature control, and secondary containment are necessary to prevent leaks or exposure during transit. Handle with appropriate safety precautions.
    Storage 4-Bromobenzenesulfonyl chloride should be stored in a tightly closed container, in a cool, dry, and well-ventilated area, away from moisture, heat, and incompatible substances such as strong bases and strong oxidizing agents. It should be kept out of direct sunlight and protected from physical damage. Store under an inert atmosphere if possible to prevent hydrolysis.
    Application of 4-Bromobenzenesulfonyl Chloride

    Applications of 4-Bromobenzenesulfonyl Chloride in Industrial Manufacturing

    As a manufacturer specializing in 4-Bromobenzenesulfonyl Chloride, we focus on supplying high-purity raw material strictly for industrial-scale transformations. The following downstream application scenarios represent the primary sectors currently utilizing this compound within established regulated workflows, where it delivers concrete process value and compliance. Each application highlights real-world standards, usage ranges, integration points, and the precise finished goods derived.

    1. Pharmaceutical Intermediate Synthesis for Active Pharmaceutical Ingredients (APIs)

    4-Bromobenzenesulfonyl Chloride serves as a recognized sulfonylation agent in the production of drug precursor molecules, especially those requiring arylsulfonyl moieties. Major pharmaceutical manufacturers employ it during multi-step syntheses of specific anti-inflammatory and anticancer API intermediates, leveraging its reactivity to introduce protective groups or as a key coupling agent in late-stage reactions.

    Industry compliance standards

    • ICH Q7: Good Manufacturing Practice Guide for Active Pharmaceutical Ingredients
    • European Pharmacopoeia (Ph. Eur.) for residual solvent and impurity controls
    • 21 CFR Part 211: FDA cGMP for Finished Pharmaceuticals
    • Japanese Pharmacopoeia for API starting materials

    Typical usage ratio

    • Applied at 0.8–1.1 molar equivalents relative to limiting amine or phenol substrates; optimized during scale-up by monitoring yield and byproduct profile

    Downstream process integration

    • Added in the protected or selective sulfonylation step, usually in anhydrous solvent, under inert gas atmosphere, prior to work-up and purification of protected intermediates

    Final product types

    • Sulfonamide, sulfonate ester, or protected aromatic intermediates for non-steroidal anti-inflammatory drugs (NSAIDs), kinase inhibitor APIs, and anti-infective development programs

    2. Electronic Grade Material Manufacturing for Photoresist Components

    The compound is critical in the custom synthesis of aryl sulfonate esters used as acid generators and functional monomers within electronic photoresist formulations. Manufacturers in display and semiconductor fabrication require precise sulfonylation for the synthesis of photoacid generator (PAG) intermediates that support advanced lithography.

    Industry compliance standards

    • IATF 16949: Quality Management Systems for Automotive Sector (for microelectronic components)
    • JEITA standards for electronic chemicals purity (Japan Electronics and Information Technology Industries Association)
    • SEMI C93: Specification for Liquid Electronic Chemicals
    • RoHS Directive 2011/65/EU for restricted substances

    Typical usage ratio

    • 0.3–0.7 molar equivalents per target functional PAG precursor; adapted to control the molecular weight and charge density in custom projects

    Downstream process integration

    • Fed to the controlled sulfonylation stage after oligomer or small molecule framework has been assembled, prior to neutralization and downstream formulation

    Final product types

    • Functionalized aryl sulfonate esters, custom PAG monomers, and intermediate resins for deep UV and EUV (extreme ultraviolet) photoresist solutions

    3. Agrochemical Intermediate Production (Herbicide/Pesticide Building Blocks)

    Major agrochemical producers incorporate 4-Bromobenzenesulfonyl Chloride as a sulfonylation reactant for synthesizing herbicide and pesticide intermediates that require the arylsulfonyl group for bioactivity. Its selectivity for certain aromatic substrates supports multi-ton batches in regulated industrial campaigns.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • ISO 9001:2015 Quality Management Systems in agrochemical manufacturing
    • REACH Regulation (EC) No 1907/2006 for chemical safety
    • US EPA Pesticide Registration (40 CFR Part 158)

    Typical usage ratio

    • Implemented at 0.9–1.2 molar equivalents per coupling partner, adjusted based on target yield and the reactivity of substrate phenols or amines

    Downstream process integration

    • Introduced during final or penultimate step of functionalization, post core scaffold synthesis, followed by hydrolysis or further coupling as needed for downstream pesticide actives

    Final product types

    • Precursor intermediates for sulfonylurea herbicides, arylsulfonyl-substituted insecticides, and related crop protection agents

    4. Dye and Pigment Intermediate Synthesis (Sulfonated Aromatic Dyes)

    Producers in the synthetic dye sector use this compound to introduce sulfonyl chloride groups to aromatic dye intermediates, enhancing solubility and reactivity during the coupling and sulfonation stages. The result is the scalable manufacture of sulfonated dye intermediates for water-soluble dyes and selected organic pigments.

    Industry compliance standards

    • OEKO-TEX Standard 100 for restricted substances in textiles
    • ZDh (German Dyestuff Association) purity and heavy metal content guidelines
    • ISO 9001:2015 for pigment and dye manufacturers
    • EPA TSCA (Toxic Substances Control Act) for chemical inventory reporting

    Typical usage ratio

    • Approximately 1.0–1.3 molar equivalents, selected per substrate based on the required sulfonation level and desired water-solubility of the final dye compound

    Downstream process integration

    • Charged during aromatics functionalization step, before azo coupling or condensation, ensuring full integration of sulfonyl group for downstream dye lot uniformity

    Final product types

    • Sulfonated azo dyes, anionic disperse dyes, and specialty pigments for textile, ink, and paper applications

    5. Polymer Crosslinking Agent Preparation (Specialty Crosslinkers in Performance Polymers)

    Select polymer manufacturers employ this specialty raw material for the controlled synthesis of aryl sulfonyl chloride crosslinkers used in performance polymer matrices. By reacting it with multi-functional nucleophilic agents, companies produce advanced crosslinkers for thermosetting resins and specialty adhesives.

    Industry compliance standards

    • ASTM D638 (Mechanical Properties of Plastics)
    • ISO 14001:2015 for environmental management in chemical processing
    • REACH pre-registration for crosslinking agents
    • GMP guidelines for indirect food contact polymers

    Typical usage ratio

    • Ranges from 0.2–0.6 molar equivalents, tailored by end-user to achieve specific gelation, curing, and mechanical property requirements in each resin system

    Downstream process integration

    • Used in pre-polymer or post-polymer functionalization steps, typically dissolved in organic solvent and introduced before chain extension or network formation

    Final product types

    • Multi-functional crosslinkers for epoxy and polyester resins, specialty adhesives, and high-performance engineered plastics

    Free Quote

    Competitive 4-Bromobenzenesulfonyl Chloride prices that fit your budget—flexible terms and customized quotes for every order.

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    Certification & Compliance
    More Introduction

    Introducing 4-Bromobenzenesulfonyl Chloride: A Look Inside Our Manufacturing and Its Value in Chemical Synthesis

    Understanding the Product and Our Approach to Quality

    Over the years, producing specialty sulfonyl chlorides has taught us the value of precision and consistency, especially with reactive halogenated intermediates. 4-Bromobenzenesulfonyl chloride—a distinctive electrophilic reagent—stands out in our catalog for its ability to deliver results without compromise. Our model, controlled synthesis, and focus on chemical purity stem not from trend but from decades of meeting the ever-stricter expectations of our partners in the pharmaceutical, agrochemical, and materials sectors.

    As the direct manufacturer, our process begins at the very basic building block. Every batch starts with pharmaceutical-grade raw materials sourced from verified long-term suppliers. Each step, from chlorosulfonation of bromobenzene to isolation and purification, has been adjusted and fine-tuned by our technical team based on real-world feedback. The product’s appearance—a pale yellow to white crystalline powder—arises from this attention to detail. What leaves our plant must reflect the nature of our raw inputs, not just pass downstream testing requirements.

    Key Specifications from a Practical Standpoint

    With 4-bromobenzenesulfonyl chloride, even small flaws can derail an entire downstream process. We have learned that pharmaceutical chemists care less about theoretical purity and more about what the product does inside a reactor. A standard assay by HPLC or GC, usually exceeding 99%, reassures our partners their results will remain reproducible, batch to batch. Moisture and acidity are tightly controlled with validated drying and packaging protocols—moisture below 0.5% directly reduces hydrolysis risk when the product gets transferred out of our drums, especially in humid climates. Any color changes or impurity spikes act as early warnings for us to halt distribution, even before a formal complaint arises.

    Most users prefer a mesh size that flows like sand. Our plant’s milling equipment always leaves a slightly granular texture, balancing flowability with dust reduction. This makes handling easier for the end-user and helps minimize accidental exposure, which matters to both chemists and line operators.

    What Sets 4-Bromobenzenesulfonyl Chloride Apart in Application

    Our team sees first-hand how 4-bromobenzenesulfonyl chloride unlocks transformations that few other sulfonyl chlorides can. Its combination of a reactive para-bromine and sulfonyl chloride group gives contract manufacturers and research labs a reliable intermediate for coupling, arylation, and selective substitution. Unlike unsubstituted benzenesulfonyl chloride, the para-bromo version opens direct routes to aryl sulfonamides, sultams, and complex heterocyclic cores.

    In our experience, a significant portion is used in multi-step pharmaceutical syntheses where precision matters more than volume. Our technical support team often helps scale up lab-scale routes for kinase inhibitors or photoactive compounds. These transformations demand not just purity, but chemically predictable reactivity without surprise side-products. In many contrast studies, generic grades from resellers led to variable yields, often due to trace organics or uneven grain size—issues minimized by tight in-house process control.

    Besides direct pharmaceutical use, our partners in polymer chemistry value the bromine as a hook for further cross-coupling. Custom ligand synthesis, for example, relies on the sensitivity of both functionalities staying intact at elevated temperature before catalyst introduction. Standard benzenesulfonyl chloride cannot achieve this, and ortho-substituted versions tend to suffer from steric hindrance and slower kinetics. Years of feedback convinced us that para-bromo substitution represents the practical sweet spot between reactivity and manageability.

    The Difference is in the Details: Sourcing from a Direct Manufacturer

    Many resellers claim to offer the same pedigree of 4-bromobenzenesulfonyl chloride, but the gap becomes obvious after a few runs in a demanding application. As the actual producer, we take direct responsibility for every critical aspect—from raw materials, synthesis controls, to post-processing and lot release. Our facility runs regular analytical method qualification by cross-titration and mass spectrometry, not simply by expected certificate printouts.

    Unlike third-party brokers, our batch records stay transparent. We trace back every deviation, be it a color shift or unexpected residue, analyzing both root cause and impact on user chemistry. Regular dialogue with end-users means our product evolves in line with the market, not behind it. The only way to maintain this trust is through continuous data sharing and responding rapidly to feedback, not stock statements about compliance and specification.

    Supply disruptions and shifting regulatory environments have only increased the value of this approach. During logistical bottlenecks, we maintain reserve stocks of raw bromobenzene and chlorosulfonic acid to buffer against unexpected events. This ensures we do not break supply chains that depend on timely delivery for time-sensitive drug and specialty material projects.

    Common Application Pitfalls and How We Address Them

    We have seen first-hand how even experienced teams overlook the volatility or hydrolytic sensitivity of sulfonyl chlorides during transfer and storage. Our advice—echoed by years of practical troubleshooting—is to store in dry, closed containers away from direct humidity sources, and to transfer only in well-ventilated, moisture-minimized environments. Several partner labs have reported clogged lines or failed reactions from using reprocessed, off-spec stock, a risk minimized by our robust quality controls and clear retest dates.

    Every shipment includes a stability window factored by measured shelf-life, not just guesswork. Our research division has confirmed that most failures come from improper repackaging or using material well beyond intended use date—an issue rarely seen by those sourcing directly from the original batch.

    Even at gram-to-kilo scale, problems such as unwanted side formation of sulfonic acids or the release of corrosive fumes during hydrolysis can arise without well-matched physical properties. By standardizing moisture and acidity controls, we help minimize health and safety risks at the bench and in process lines, improving user safety and final product yield.

    Comparing with Similar Sulfonyl Chlorides and Market Alternatives

    It is tempting to swap benzenesulfonyl derivatives without giving much thought to substitution effects. Over our history, we have fielded requests to replace 4-bromobenzenesulfonyl chloride with lower-cost benzenesulfonyl chloride or other halogenated variants such as 2-bromobenzenesulfonyl chloride and 4-chlorobenzenesulfonyl chloride. The reality: such swaps often lead to unpredictable results. Ortho substitution usually leads to sluggish kinetics by introducing steric hindrance that disrupts nucleophilic attack. Chloro analogues sometimes offer similar reactivity, but the bromo species’ activation potential in cross-coupling, especially for Suzuki or Buchwald-Hartwig reactions, simply cannot be matched.

    Many generic suppliers overlook these differences, often blending lots or selling off-grade material with higher impurity loads. For research or scale-up where minute amounts of impurity can catalyze side-reactions, true para-bromo purity translates to direct project savings and less troubleshooting. Where fiber and specialty plastics manufacturers exploit the dual reactivity sites for advanced polymer architectures, even minor contamination wrecks product uniformity. Our team takes feedback from these failures and adjusts not just our own process, but also the advice we give to other research chemists and scale-up engineers.

    Supporting Our Clients’ Evolving Needs

    Markets keep shifting. Pharmaceutical, fine chemical, and polymer research now demand not only functional reactivity but documentation, traceability, and safety data with every kilogram. Our in-house QC lab updates test protocols regularly, reflecting advancements in chromatographic and spectroscopic techniques. None of these changes happen in a vacuum—they are a direct response to actual customer audits and industry regulatory shifts. Recently, an uptick in demand from peptide synthesis prompted us to revalidate residue and trace halide levels, directly reducing batch rejection rates for our partners.

    User needs do not stop at chemical properties. Packaging, for one, matters far more than most realize. Our drums, lined with HDPE and layered for moisture resistance, help our clients avoid the waste and lost time of caking or clumping. Real-world feedback, including reports of wasted hours breaking up solidified product from older sources, pushed us to invest in rigorous post-packaging checks. None of our competitors bring the same manufacturing-level insight to this part of the supply chain.

    We also nurture a culture of transparency. Customer laboratories often request tailorable lot sizes or minor spec variations for unique projects. Rather than shuffling this upstream to an unknown producer, our plant supervisors and technical sales team work hand-in-hand to deliver material with little lead time, documented pedigree, and precise analytical data. This hands-on model helps both large and small partners meet accelerated project timelines and pass the surprise audits becoming common in regulated markets.

    The Human Element: Safety, Environmental Responsibility, and Experience

    Years of direct synthesis experience have shown us the real risks behind halogenated sulfonyl reagents. Thermal hazards in scale-up, moisture-driven fuming, and incompatible transfer equipment have all generated plant incidents elsewhere in the industry. Instead of ignoring these realities, we hold regular safety workshops to review incidents and update protocols for our own staff, a discipline mirrored by the advice we give to end-users. We never treat safety as an afterthought or as the customer’s responsibility alone.

    Environmental mandates around waste halides grow more stringent each year. In response, we upgraded effluent handling to neutralize residual chlorides and bromides, choosing methods that reduce aquatic toxicity without creating secondary hazards. Customers in the EU and North America often ask about our environmental practices, and we welcome those reviews because they push us to advance past simple compliance. By sharing environmental impact reports and waste-handling solutions, we help downstream partners avoid rejection and penalties as well—something unattainable with generics or poorly sourced intermediates.

    Closing Thoughts from the Plant Floor

    Chemistry often appears abstract or distant to those outside the factory or laboratory, but manufacturing 4-bromobenzenesulfonyl chloride brings home how much detail and responsibility goes into each shipment. Our people, many with decades of experience, follow the product from its smallest batch to its final drum and even on to the dock. Failures in traceability, shortcut processing, or ignoring end-user feedback stand out quickly—a fact that leads us to value every successful project our partners deliver.

    The product reflects not just formula and purity, but a hard-earned legacy of problem-solving and innovation. For partners working at the edge of discovery or scale-up, our experience adds consistency and reliability. When a new route or material emerges, we listen and adapt because that feedback sharpens every facet of what we do on the plant floor, in the QC lab, and at every level of the business.

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