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HS Code |
212429 |
| Chemical Name | 2,4-Dibromobenzenesulfonyl chloride |
| Cas Number | 135-32-2 |
| Molecular Formula | C6H3Br2ClO2S |
| Molecular Weight | 338.41 g/mol |
| Appearance | White to off-white crystalline solid |
| Melting Point | 81-83 °C |
| Boiling Point | Decomposes |
| Density | 2.13 g/cm3 |
| Solubility | Reacts with water, soluble in organic solvents |
| Purity | Typically ≥98% |
| Storage Conditions | Store in a cool, dry, well-ventilated area away from moisture |
| Synonyms | 2,4-Dibromo-benzenesulfonyl chloride |
| Inchi Key | OWFQYCPNFEYHJK-UHFFFAOYSA-N |
| Smiles | C1=CC(=C(C=C1Br)Br)S(=O)(=O)Cl |
As an accredited 2,4-Dibromobenzenesulfonyl Chloride factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 500g of 2,4-Dibromobenzenesulfonyl Chloride is packaged in a white, sealed HDPE bottle with proper hazard labeling and tamper-evident cap. |
| Shipping | 2,4-Dibromobenzenesulfonyl Chloride should be shipped in tightly sealed containers, protected from moisture and incompatible substances. It must comply with hazardous materials regulations, typically under UN 3261 (Corrosive Solid, Acidic, Organic, n.o.s.). Use appropriate labeling and documentation, and transport via ground or air by certified carriers following ADR, IATA, or IMDG guidelines. |
| Storage | 2,4-Dibromobenzenesulfonyl chloride should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area. Keep away from moisture, heat sources, and incompatible substances such as strong bases, oxidizing agents, and water. Store under inert gas if possible to prevent hydrolysis. Use secondary containment to avoid environmental contamination and ensure safe handling with proper personal protective equipment. |
Applications of 2,4-Dibromobenzenesulfonyl Chloride in Industrial ManufacturingAs an established producer of 2,4-Dibromobenzenesulfonyl Chloride, we supply this intermediate to major manufacturers integrating into complex synthesis routes. The compound delivers essential functionality in sectors requiring high-purity aromatic sulfonyl chlorides for stepwise chemical transformations. Below, we present key industrial applications, each with distinct downstream integration, compliance frameworks, and typical usage profiles. 1. Pharmaceutical Intermediates SynthesisPharmaceutical companies use 2,4-dibromobenzenesulfonyl chloride for producing advanced intermediates in the synthesis of APIs, especially where specific brominated aromatic sulfonyl linkages are required. Our material supports the construction of selective enzyme inhibitors and oncology compounds. Manufacturers optimize chlorosulfonation and bromination steps employing this raw material under GMP-controlled workflows, ensuring batch consistency and full traceability. Integration typically occurs before heterocycle formation or as a capping agent for subsequent derivatization. Industry compliance standards
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2. Agrochemical Synthesis (Herbicide and Pesticide Precursors)Formulators of advanced crop protection agents rely on 2,4-dibromobenzenesulfonyl chloride for constructing sulfonyl-linked agrochemical actives. This material enables the assembly of sulfonamide and brominated phenyl core structures, essential for modern herbicides requiring high potency and environmental persistence. Integration occurs in the early-phase functionalization of bulk actives, with tight in-process controls to assure product integrity and process safety. Material specification and consistency play a critical role within regulatory dossiers and stewardship programs. Industry compliance standards
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3. Specialty Polymer ModificationProducers of high-performance engineering plastics and resins incorporate 2,4-dibromobenzenesulfonyl chloride as a bridge for introducing both bromine and sulfonyl groups into polymer backbones. This approach imparts flame retardancy and enhanced chemical resistance to specialty polymers, such as polyethersulfone and aromatic polyimides. We supply material to extrusion and solution polymerization facilities where controlled dosing and precise addition profiles deliver repeatable macromolecular architecture. The application ensures final polymer grades meet the stringent safety regulations for electronics and transportation. Industry compliance standards
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4. Organic Electronic Material SynthesisManufacturers of advanced electronic chemicals utilize 2,4-dibromobenzenesulfonyl chloride for constructing organic semiconductor intermediates. This material provides brominated and sulfonyl functionality tailored for organic light-emitting diode (OLED) and hole-transport materials through precise substitution on aromatic systems. Integration into Suzuki-Miyaura or direct arylation reactions requires high-purity grades to avoid trace metal and halide contamination. Batch records, full spectral documentation, and custom packaging support downstream device assembly and pilot-scale validation. Industry compliance standards
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5. Custom Dye and Pigment ManufacturingProducers of specialty dyes and performance pigments use 2,4-dibromobenzenesulfonyl chloride to introduce unique halogen-sulfonyl substitution patterns in organic colorants. This enables the synthesis of water-resistant and lightfast dyes for technical textile, industrial ink, and toners. The compound enters controlled sulfonation and substitution processes monitored for batch color consistency and contaminant profile. We provide customizable lot sizes with COAs matching analytical reference spectra for downstream pigment compounding or dye blending. Industry compliance standards
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Day after day, our team moves from the pilot plant to full-scale reactors, preparing specialty intermediates for both research labs and industrial production lines. Among these, 2,4-dibromobenzenesulfonyl chloride holds a prominent place, not just due to its unique reactivity but for the consistency and reliability it brings to each synthetic step in the development of pharmaceuticals and fine chemicals. We produce this compound starting from high-purity dibromobenzene, ensuring that throughout chlorination and sulfonation reactions, operational controls remain strict. Our technical staff track every batch from raw material selection to finished packaging, with regular in-process quality checks. This approach means our customers see consistent color and purity, two factors that impact performance in both lab-scale research and plant-scale manufacturing.
2,4-Dibromobenzenesulfonyl chloride appears as a pale yellow to off-white crystalline powder, distinctly aromatic in odor, with a characteristic melting range that confirms its integrity. Hydroscopicity matters a great deal to chemists using this material. We pack our product under nitrogen and with moisture-resistant linings, because exposure to air can induce unwanted hydrolysis, forming the corresponding sulfonic acid. Inconsistent handling during packing or storage leads to clumping and a drop in yield for end users. On site, we monitor stability with accelerated aging tests and stress conditions: no surprises shift downstream costs or process development results. Each kilogram passes tight purity targets, generally exceeding 98.5% by HPLC, while we routinely remove trace organics and heavy metal impurities with proprietary purification steps.
Early attempts to scale the sulfonylation reaction revealed a lot about the character of 2,4-dibromobenzenesulfonyl chloride. The reactivity of both bromine atoms with sulfonyl chloride groups is a delicate balance. On one hand, we maintain batch homogeneity with carefully regulated temperature profiles; on the other, any deviation can lead to unwanted byproducts, especially poly-sulfonated species or overchlorination. Unlike spec sheets, hands-on experience shows how minor fluctuations in crystallization solvents or drying conditions influence the free-flowing nature of the powder. If the product cakes or carries microscopic metal residue, downstream customers lose not just time, but raw material to clean-up and extra purification; these hard-earned lessons led us to introduce continuous wet-milling and high-vacuum methods to deliver a purer, more manageable intermediate.
Control at each step translates into tight particle size distribution, consistent reactivity, and fewer storage complications. This directly impacts anyone scaling up amid tight deadlines or working in temperature- and humidity-sensitive processes, especially in pharmaceutical intermediates where batch reproducibility gets scrutinized. Manufacturing at scale curtails batch-to-batch variability down to a narrow margin, so project managers and bench chemists alike meet internal quality demands and downstream regulatory reviews.
In our daily work, conversations with process chemists, synthetic teams, and formulation scientists often circle back to the role of 2,4-dibromobenzenesulfonyl chloride as a coupling and activating agent. The sulfonyl chloride moiety reacts efficiently with amines and alcohols, forming sulfonamides and sulfonate esters—classic motifs across many drug candidates and agrochemicals. Its two bromine atoms offer valuable positions for further functionalization, particularly in Suzuki-Miyaura coupling and other palladium-catalyzed cross-couplings. Through countless pilot runs and feedback from contract manufacturing organizations, we’ve seen how its clean leaving group profile supports step economies, reducing the need for post-reaction neutralization or resource-heavy purification protocols.
This compound appears most often in medicinal chemistry, custom synthesis, and advanced materials. Large pharmaceutical firms routinely request multi-hundred kilogram lots for API precursor synthesis. Fine chemical researchers favor it for constructing functionalized aromatics needed in organic electronics and specialty polymers. Years of feedback show that kitting out process runs with our material, which carries fewer residual starting materials and less chlorinated byproduct, means one less variable to account for during scale-up. Feedback loops direct us to keep analytical support transparent, with full NMR, FTIR, and mass spectrometry data sets accompanying every shipment when requested.
Working as the original manufacturer, not as a trader or reseller, means we track every point of comparison between our 2,4-dibromobenzenesulfonyl chloride and structurally similar reagents. Classic sulfonyl chlorides such as benzenesulfonyl chloride or p-toluenesulfonyl chloride form the backbone of many industrial processes—they offer rapid reactivity and wide usage but lack the functional group diversity needed in research-driven fields. In replacing them, dibromo derivatives introduce distinct advantages in modern molecule construction. The two bromines enable sequential coupling or halogen-metal exchange, a feature not available in simpler analogs.
We supply large custom synthesis clients with both mono- and di-brominated sulfonyl chlorides, and over years of field feedback, the 2,4-dibromo variant stands out for its dual-use. It serves as both an electrophile and as a point for further aromatic modification, expanding reaction options in downstream laboratories. This flexibility drives interest among R&D chemists pushing into new territory, searching for aryl sulfonylation of sensitive fragments. Competitor products—often sourced from multi-stage traders—have been found with inconsistent purity or with halide ratios outside of specification. This occurs when supplier networks extend too far from the source, diluting process accountability, and raising the risk of cross-contamination with other halogenated aryl intermediates.
Earlier collaborations with academic and industrial research partners exposed just how much batch-to-batch uniformity matters. For instance, drift in halide content or sulfonyl chloride activity affects yields in formation of sulfonamides. We track such details with real-time spectroscopy and random batch sampling, committing these findings to continuous process improvement.
As a chemical producer, practical hurdles define laboratory and plant-floor routines. 2,4-dibromobenzenesulfonyl chloride presents particular storage and handling needs. Moisture triggers hydrolysis, forming undesired side-products that show up as off-target peaks during method development or quality release. Each drum gets tested for residual moisture and packed under conditions learned from years of failures and successful shipments. The outer bags accompany desiccant packs, and we request that clients draw down only the amount required per shift. This guidance comes from working through dozens of real-world incidents where product lost specification due to brief excess air or humidity exposure.
Shipping and packaging remain constant concerns. Shipments moving over long distances face vibration and climate variation far greater than conditions inside a static warehouse. In our own supply chain, we rotate finished stock FIFO-style, limiting age before dispatch, and train logistics partners on the difference between high-value, reactive intermediates and general bulk chemicals. If cartons stack incorrectly, soft crystalline product forms, clogging lines and slowing subsequent dissolution or reaction. Adjusting the physical properties of the product often begins at the synthesis or crystallization stage. For example, tweaking the crystallization solvent mix can change the powder’s friability, preventing it from forming stubborn lumps during shipping or transfer.
Team meetings rarely focus on just technical targets; we analyze client complaints and lab troubleshooting notes, using every event to reinforce our process training. Regulatory audits also push us to track not only the quality quirks of 2,4-dibromobenzenesulfonyl chloride, but also its environmental health profile. Pre-treatment of waste streams from the plant involves separating acidic byproducts and exhaustive ventilation of process areas where volatile residues build up—improvements adopted after targeted risk assessments led by our EHS staff alongside third-party inspectors.
Authentic manufacturing experience reveals details omitted by distribution chains. It’s not just about purity, but about confidence in every drum that leaves our facility. Teams in our quality control lab, equipped with advanced chromatography, conduct near-line testing multiple times each shift. They investigate batch anomalies—color changes, unusual odors, unexpected melting point drift—before release clears the product for final packing. Recalls or complaints from end users hit everyone along the supply chain; preventing them requires real-time intervention rather than after-the-fact adjustments.
Standardization across global manufacturing sites is never trivial. Variability in raw materials, temperature, or operator technique produces subtle shifts in the final product fingerprint. Site managers and R&D teams collaborate to bake lessons learned into site-specific process controls. For 2,4-dibromobenzenesulfonyl chloride, we long ago switched to centralized process documentation, accessible by both production and QA. Minor deviations flagged upstream in synthesis or purification receive immediate attention, since the speed and severity of halide or moisture intrusion can escalate rapidly. Downstream users get the benefit: shorter lead times, and product that supports clean, reproducible reactions every time.
Real engagement with customers and researchers—rather than anonymous market surveys—steers how we formulate and deliver our product. Case studies emerge organically as customers send back run logs and yield reports. When a process fails to deliver expected conversion rates, we dive into the specifics: solvent composition, heating rates, order of addition, and even operators’ histories working with sulfonyl chlorides. Many of these issues stem from slight mismatches in physical form or trace byproduct levels. Our team responds with product improvements based on close reading of application data, modifying milling parameters or switching crystallization agents to match process needs. We never treat such learning as one-way; our partners’ insights change our SOPs, training, and packing workflows each year.
Regular visits to customer sites reveal practical hurdles not obvious from technical data sheets. In several cases, pilot-plant operators found that our lot-to-lot control let them streamline their reagent charging procedure, minimizing unreacted chloride or halide contamination in downstream columns. One client reported that subtle differences in powder density led them to change solvent ratios, realizing a spike in yield without new capital investment. These incremental advances drive our team to keep chasing better handling, improved shelf life, and reduced batch failures.
Producing organosulfur chlorides like 2,4-dibromobenzenesulfonyl chloride calls for steady vigilance in environmental impact and worker health. The reactivity that makes this compound valuable also creates challenges: accidental spills or improper venting can liberate corrosive fumes or halogen byproducts. To address this, plant layout features closed transfer systems, double-jacketed vessels, and local exhaust extraction at all points where solids or vapors might escape. Staff receive targeted training on PPE, emergency measures, and spill containment.
Effluent streams get tested for both free chlorine and bromide ions before release to the site wastewater plant. Over years, we invested in carbon scrubbing and advanced neutralization facilities, going well beyond basic compliance. This focus on controlled risk underpins our relationship with clients who themselves face mounting regulatory scrutiny both locally and internationally. Transparency in batch records, analytical data, and safety documentation gives procurement and QA departments full visibility before product hits their dock.
We partner with local emergency response teams to review plant layouts and update action protocols. Annual audits—led by external consultants and internal EHS professionals—inject fresh perspective and spark updated hazard controls. Open lines with customer EHS officers have influenced not just product stewardship but entire process upgrades, reinforcing a community of safe and responsible handling of 2,4-dibromobenzenesulfonyl chloride.
Direct involvement in the lifecycle of 2,4-dibromobenzenesulfonyl chloride—from synthesis to finished product—brings practical advantages every day. Clients gain direct access to source-level technical support; we supply not just material but the process know-how embedded in each batch. From supporting custom chemical development projects to establishing reliable supply chains for critical intermediates, the lessons gathered on the shop floor and in the QC lab differentiate what we send out into the world.
Manufacturing is a commitment—to end users, to partnership, and to the compound’s evolving role in science and industry. Every improvement feeds back into our processes, and every challenge gets met with direct action on the ground. In doing so, we support not just the immediate needs of chemistry teams worldwide, but the wider ecosystem that depends on safe and robust industrial chemistry.