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2,5-Dibromobenzenesulfonyl Chloride

    • Product Name 2,5-Dibromobenzenesulfonyl Chloride
    • Alias 2,5-DBBSC
    • Einecs 253-520-5
    • 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
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    Specifications

    HS Code

    348995

    Chemical Name 2,5-Dibromobenzenesulfonyl Chloride
    Cas Number 20265-97-8
    Molecular Formula C6H3Br2ClO2S
    Molecular Weight 336.41 g/mol
    Appearance White to off-white solid
    Melting Point 93-95°C
    Solubility Reacts with water, soluble in organic solvents like dichloromethane
    Purity Typically ≥ 98%
    Smiles C1=CC(=C(C(=C1Br)S(=O)(=O)Cl)Br)
    Inchi InChI=1S/C6H3Br2ClO2S/c7-4-1-2-6(9(10,11)12)5(8)3-4/h1-3H

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

    Packing & Storage
    Packing A 25-gram amber glass bottle with a tightly sealed cap, labeled with hazard warnings and chemical identification details for 2,5-dibromobenzenesulfonyl chloride.
    Shipping 2,5-Dibromobenzenesulfonyl Chloride should be shipped as a hazardous material in accordance with local, national, and international regulations. Use tightly sealed containers, clearly labeled, and pack with appropriate cushioning materials. Avoid exposure to moisture and extreme temperatures. Handle and transport only by trained personnel following safety and environmental guidelines.
    Storage 2,5-Dibromobenzenesulfonyl chloride should be stored in a tightly sealed container, away from moisture, heat, and direct sunlight. Keep in a cool, dry, and well-ventilated area, separated from incompatible substances such as strong bases, alcohols, and amines. Store in a designated corrosive chemical cabinet and ensure proper labeling. Avoid exposure to air to prevent hydrolysis and decomposition.
    Application of 2,5-Dibromobenzenesulfonyl Chloride

    Applications of 2,5-Dibromobenzenesulfonyl Chloride in Industrial Manufacturing

    As a direct manufacturer, we provide 2,5-dibromobenzenesulfonyl chloride to select advanced chemical sectors. Our product integrates into specialized downstream formulations with specifically engineered benefits, supporting strict compliance and quality objectives in demanding industrial environments. Below, we present authentic application routes based on real-world practice.

    1. Active Pharmaceutical Ingredient (API) Intermediate Synthesis

    Major pharmaceutical companies deploy our material in multi-step synthesis of sulfonamide-based APIs, particularly where aromatic sulfonyl chloride moieties enable subsequent coupling or cyclization reactions. The highly selective reactivity facilitates efficient intermediate preparation for targeted therapeutic classes, including anti-infectives and certain oncology candidates, meeting the industry's requirement for traceability and batch reproducibility.

    Industry compliance standards

    • ICH Q7 GMP for Active Pharmaceutical Ingredients
    • US FDA 21 CFR Part 210/211
    • EU EudraLex Volume 4
    • Relevant pharmacopoeia reference (USP, Ph. Eur.) based on downstream API registration

    Typical usage ratio

    • Added at 0.8–2.5 molar equivalents relative to key aromatic amine intermediates; stoichiometry adjusted based on batch size, target yield, and impurity profile requirements

    Downstream process integration

    • Charged into protected or nitrogen-inert vessels during initial sulfonylation/coupling; follows solvent charging and temperature ramping, prior to introduction of nucleophile for next synthetic transformation

    Final product types

    • Sulfonamide class APIs (e.g., antibacterials, kinase inhibitors)
    • Pharmaceutical intermediates for clinical development

    2. Agrochemical Intermediate Manufacturing

    Crop protection chemical producers utilize this compound to construct brominated benzenesulfonyl derivatives as core intermediates for selective herbicides and fungicides. The precise double bromine substitution supports downstream reactivity patterns essential for high-activity formulations. Industrial production workflows exploit its batch consistency and purity to control reactant profiles in regulated and audited plants.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • ISO 9001:2015 Quality Management (applicable to agrochemical synthesis)
    • Relevant REACH requirements for handling and traceability
    • Responsible Care Program compliance (ICCA members)

    Typical usage ratio

    • Primarily 0.9–1.1 molar equivalents versus nucleophilic aromatic precursors; fine-tuned during pilot scaling to balance conversion rate and impurity minimization

    Downstream process integration

    • Introduced in closed system reactors post-solvent charging, often under chilled, stirred reaction with alkali or other functionalized aromatic reactants to form a brominated sulfonylated core

    Final product types

    • Brominated herbicide intermediates
    • Fungicide precursors for commercial formulation
    • Active agrochemical ingredient building blocks

    3. Specialty Polymer Additive Production

    Leading polymer manufacturers employ this substance in the synthesis of functionalized aromatic sulfonyl chloride monomers. These monomers endow finished polymers with enhanced flame retardancy or chemical resistance, integrating efficiently into custom resin chains by co-polymerization. Our raw material’s purity and stability are critical to avoid color or performance variation in high-value engineered plastics.

    Industry compliance standards

    • ISO 14001:2015 (for environmental management in chemical operations)
    • UL 94 (Flammability of plastic materials)
    • RoHS Directive (2011/65/EU, for electronics applications)
    • Regulation (EC) No 1907/2006 (REACH) for polymer precursors

    Typical usage ratio

    • Used at 5–25% by weight in functional monomer synthesis batches; proportion specified by target flame retardant property and copolymer composition

    Downstream process integration

    • Fed during controlled monomer synthesis after initial aromatic core formation; introduced at the sulfonylation stage, then subsequently polymerized via copolymerization or grafting in resin production units

    Final product types

    • Flame-retardant engineering plastics
    • Halogenated specialty polymer additives
    • Modified polysulfone and polyarylate resins

    4. Electronic Chemical Manufacturing (Photoresist and Etchant Components)

    In electronics chemical production, particularly for the fabrication of advanced photoresists and fine pattern etchants, this raw material acts as a high-purity precursor for sulfonyl chloride-based functional groups. This enables electronic material suppliers to fine-tune thermal and chemical profiles critical for semiconductor wafer processing. Stringent qualification for ion contamination and microstructure stability underpins its select applications.

    Industry compliance standards

    • SEMI S2 and S8 (semiconductor material environmental, health, and safety)
    • JEITA EHS Guidelines (Japan Electronics and Information Technology Industries Association)
    • ISO 9001/14001 (quality and environmental for electronics chemicals)
    • Customer-mandated ionic contamination thresholds (typically <1 ppm for key ions)

    Typical usage ratio

    • Integrated at 0.5–1.2 molar equivalents, relative to target precursor volume, with microdosing for process-sensitive lines

    Downstream process integration

    • Dosed in microfilm batch reactors or inline mixing heads during the synthesis of advanced photoactive compounds and patterning etchant blends

    Final product types

    • Sulfonated photoresist materials
    • Etchant precursors for photolithography and semiconductor cleaning
    • Advanced material blends for wafer surface treatment

    5. Fluorochemical Intermediate Preparation

    Producers of performance fluorochemicals use this dichlorinated sulfonyl chloride to introduce reactive sulfonyl groups before or after fluorination steps, facilitating the construction of custom-tailored fluorinated benzenes for demanding applications, including coatings and high-performance surfactants. Its specific bromine placement enhances selectivity and reactivity in controlled halogen-exchange or substitution reactions common to this sector.

    Industry compliance standards

    • OECD Guidelines for Chemical Testing and Safety
    • REACH Pre-manufacture Notification (for fluorinated intermediates)
    • ISO 9001/14001 for specialty chemicals
    • Company-level protocols for PFAS/PFOA risk management and disclosure

    Typical usage ratio

    • Processed at 1.0–2.4 equivalents to base aromatic substrate, based on fluorination target and substitution pathway optimization

    Downstream process integration

    • Charged in prefluorination or postfluorination reaction steps, depending on desired functional group placement, often in solvent-controlled reactor trains with online analytical verification

    Final product types

    • Fluorinated performance chemicals for industrial coatings
    • Custom-fluorinated intermediates for specialty surfactants
    • High-purity starting materials for electronics-grade fluoropolymers
    Free Quote

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    Certification & Compliance
    More Introduction

    2,5-Dibromobenzenesulfonyl Chloride: The Backbone of Reliable Synthesis

    A Closer Look at 2,5-Dibromobenzenesulfonyl Chloride—More Than Just a Reagent

    In the chemical manufacturing business, repeatability and reliability matter every single day. Making 2,5-dibromobenzenesulfonyl chloride in our own reactors, with steady hands and sharpened methods, speaks to a story of practical experience and constant refinement. We approach each batch with the same dedication as the last, never underestimating the role of small steps in delivering quality. On rolls of labeling tape or in the hearts of vessels heated with steam, tiny choices and carefully weighed raw material keep the process honest—from the reaction flask to the tightly sealed drum.

    Our work with aromatic sulfonyl chlorides stretches back decades, and we've come to respect the differences a single halogen atom makes. 2,5-dibromo substitution brings unique reactivity, impacting everything from process safety to the selectivity of downstream products. We handle every container knowing that both bromine atoms matter—not just as theoretical points on a structure diagram, but as tangible variables in real chemistry. The structure, C6H2Br2SO2Cl, defines its behavior, its hazards, and its opportunities in labs and plants around the world. Yet, until you have poured out the crystalline powder yourself, and inhaled its distinct—if not always pleasant—odor during transfer, you cannot fully know a material’s practical quirks.

    Production Experience Sets Us Apart

    Working from raw benzene derivatives, each stage of our synthesis receives full attention. There are manufacturers who take shortcuts—rushing temperature ramps, under-mixing, or neglecting thorough drying after the sulfonation. We do not entertain such practices. Product consistency grows from discipline, not chance. Our team tracks every anomaly, double-checks system cleanliness after maintenance, and tests for trace contaminants that could alter a reaction’s course. Even a slight impurity or minor overreaction can haunt a batch, showing up later as off-color solution or low reaction yield for the formulator.

    2,5-dibromobenzenesulfonyl chloride doesn’t get the spotlight that some broader-use chemicals receive, but for those who depend on it, reliability tops every requirement list. Our clients have told us how a single lot discrepancy brought months of project delays, calling for late-night troubleshooting and significant financial loss. With specialty sulfonyl chlorides like this, even a one-off variability can ripple out, breaking trust and scrambling timelines. Accountability keeps our process honest; our reputation for consistency has taken years, not months, to build.

    Down-to-Earth Advantages and Application Experience

    In organic synthesis, the genuine difference between a successful scale-up and a frustrating stumbling block often lies in material choice. 2,5-dibromobenzenesulfonyl chloride reacts with amines and alcohols to form sulfonamides and sulfonate esters. These groups sit at the foundation of advanced intermediates for agrochemicals, pharmaceutical precursors, and custom material coatings, among other uses. We have sat down with R&D chemists who hit roadblocks after switching from a cleaner sulfonyl chloride to a less-defined alternative. Not every lot of material delivers the same level of conversion or minimal by-products, and that’s where direct, batch-by-batch manufacturing control makes a real impact.

    Chemical plants demanded a product which didn’t cause unnecessary filter clogs from fine-particled residues. Analytical labs cared about traces of ferric or other metallic impurities, which could interfere with downstream chromatography. To meet these demands, we committed to tight process control, rigorous testing, and flexible packaging. Each lot is tested not just for major purity indices, but for trace elements we know from experience can wreak havoc on delicate reactions. We routinely ship in either double-lined fiber drums or small glass containers, based on user feedback about exposure risks and ease of handling in busy environments.

    Significance of Key Specifications in Real-World Use

    Purity doesn’t simply show up as a number on a certificate. Slight differences in melting point or moisture can swing synthesis results, especially for reactions that hinge on high conversion efficiency or reactivity with delicate nucleophiles. Some users need sub-percent levels of impurities, and we have honed our process for those who demand more than 98% purity by HPLC. Moisture sensitivity calls for tight storage protocols and packaging built for real transport conditions. We maintain direct contact with logistics teams—no outsourcing of responsibility—to minimize risks from rough handling, temperature swings, or long customs clearance delays.

    In practical terms, users report batch-to-batch consistency as the key difference between us and third-party distributed material. They see less ‘waxy’ product or less sticking between granules, and this cuts down on weighing errors and dust. Smaller particle size variation reduces the chances of local overheating, ghost peaks in analytics, or incomplete solution in larger scale operations. These details rarely get written in big letters on marketing pieces, yet make the daily work of chemists, technicians, and plant operators more predictable and safer.

    The Human Element and Our Commitment to Safer Handling

    Sulfonyl chlorides demand respect. Their reactivity and corrosiveness require ample caution—real gloves, working fume extraction, and no exceptions for short cuts. We provide detailed SDS packs for each shipment, but the lived experience counts just as much. We have seen what happens during an accidental splash: halting everything, adjusting protocols, retraining a team member on the spot. Older colleagues share stories about narrow escapes and how a missed venting step triggered overpressures in a poorly maintained receiver tank. Drawing from these lessons, we reinforce a safety-first attitude during every stage of material transfer, storage, and even waste disposal.

    Environmental responsibility has grown from an afterthought to an embedded part of our operations. Halogenated byproducts, acidic wash solutions, and residual traces require careful neutralization and regulatory-compliant disposal. Leaning on best practices, not minimum legal requirements, reduces headaches and ensures we don’t just shift risks downstream onto others. Close relationships with waste handlers, robust monitoring of effluent, and continued updates to our emission control technology keep us accountable not just as manufacturers, but as members of a broader community.

    Comparing 2,5-Dibromobenzenesulfonyl Chloride to Analogues—Practical Impacts

    We produce several sulfonyl chloride derivatives, from monosubstituted brominated benzenes to those with alternative halogens or ring positions. The 2,5-dibromo version sets itself apart in several day-to-day respects. Its reactivity profile favors more selective sulfonation in crowded environments—useful for pharmaceutical work requiring fewer by-products and easier purification. Compared to the 2,4-dibromo analogue, the 2,5-position layout shortens routes for making specific heterocyclic intermediates, favored in modern crop protection chemistry.

    From a handling perspective, the crystalline form of 2,5-dibromobenzenesulfonyl chloride flows differently from its lower-brominated cousins, avoiding some of the clumping or static charging issues seen in less substituted materials. The denser final product packages more securely in bulk shipping and survives longer-term storage without caking or serious degradation. This points to a pragmatic field lesson: not all ‘similar’ chemicals act the same during production, storage, or use.

    Commercial procurement teams often try to swap in parallel chemicals based on superficial similarity of structure. Chemists with enough failures under their belt learn to be wary. We have supported customers through entire development cycles, troubleshooting not just yield but also crystallization habits, shipping hazards, and unexpected side reactions. Our in-house process improvements, and collaboration with end users, keep us vigilant about any subtle shifts that could impact performance.

    Supporting Critical Applications in Industry and Research

    End uses for 2,5-dibromobenzenesulfonyl chloride often demand more precision than simple bulk chemical supply. Pharmaceutical discovery groups depend on it as a building block for sulfonamide and arylated intermediates, with demanding requirements not just for the parent compound but for each downstream transformation. In specialty polymer synthesis, its unique dibromo pattern enables unique substitutions and cross-linking points, shaping the mechanical and conductive properties of engineered polymers. Our feedback conversations with these end users highlight where process tweaks—like washing steps or drying conditions—lead to meaningful differences in final outcomes.

    Even outside the lab, manufacturers report the benefit of high-purity, low-residue sulfonyl chlorides for anti-corrosion coatings, dye intermediates, or flame retardant frameworks. Their QA inspectors depend on the predictability of melting range, moisture, and trace side-product profile to sign off on each stage of a production run. Several times, customers required full traceability on raw material origins due to regulatory scrutiny, and our in-house stewardship—zero third-party blending or repacking—supported a seamless paper trail from batch to finished product.

    Continuous Improvement: Facing Challenges and Embracing Change

    Even after producing this compound hundreds of times, we do not assume the process will always run smoothly. Variations in starting material batches, atmospheric moisture, and subtle changes in operator timing can affect overall process performance. We invest in regular retraining and in reviewing process data, treating every ‘near miss’ or off-spec incident as a chance to build better systems. Honest communication within the team and with our customers helps us maintain a transparent, responsible manufacturing environment—one that adapts and improves instead of just reacting to problems as they arise.

    Newer analytical techniques, from advanced chromatography to trace-level mass spectrometry, have pushed us to identify and remove previously overlooked contaminants. We stay active with industrial consortia and local regulatory updates, adjusting our formulation and purification protocols to keep quality and compliance up to date. Given our reliance on globally sourced raw materials, we maintain second-source options and redundant controls for critical process steps, sidestepping supply chain disruptions and keeping lead times short for our clients.

    Building Trust Through Direct Experience

    Many who come to us with stories of failed batches or disappointing pilot runs later return for the reassurance of experience-backed quality. This trust rests not on flashy brochures or endless paperwork, but on open, consistent communication and visible performance. Customers recognize the value in clarity: easy access to technical contacts, quick answers about lot history, and straightforward troubleshooting support, not layers of sales intermediaries. They remember the relief in finally getting the batch that works, or seeing analytical results that stack up perfectly after a long stretch of troubleshooting.

    Our production facility isn’t filled with high-gloss marketing or generic mission statements. Instead, success is built on the daily, practical foundation of equipment checks, regular calibration, and the lived knowledge of what makes 2,5-dibromobenzenesulfonyl chloride a dependable cornerstone for advanced synthesis. Whether in kilograms for research or larger lots rolling out under the watchful eye of our logistics crew, each shipment marks the result of hands-on technical skill and commitment.

    Looking Ahead—Meeting Evolving Needs

    Chemists, engineers, and procurement specialists set ever-tighter standards for quality, documentation, and transparency. Having worn many of these hats ourselves, we listen to feedback and adapt, rather than waiting for change to force our hand. Continued investment in process automation, trace-level analytics, and operator education keeps our product at the leading edge of reliability. We routinely host knowledge exchanges with users in applied settings, learning firsthand what real-world difficulties arise in bench work or plant operations. Those experiences cycle directly into improved methods, fewer headaches for end users, and a culture that values shared success.

    2,5-dibromobenzenesulfonyl chloride may not make headline news in most fields, but its performance quietly shapes breakthroughs across chemistry, materials science, and biotechnology. We take pride in producing a material where every detail, from structure to packaging, draws on real-world expertise. For those building tomorrow’s molecules, we stand ready with more than just a product—with the accumulated knowledge and reliable process behind each shipment.