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HS Code |
316365 |
| Cas Number | 13344-34-0 |
| Molecular Formula | C6H3Cl2O2SCl |
| Molecular Weight | 243.52 g/mol |
| Appearance | White to off-white crystalline powder |
| Melting Point | 80-83°C |
| Boiling Point | 332.1°C at 760 mmHg |
| Density | 1.64 g/cm3 |
| Solubility | Reacts with water, soluble in organic solvents |
| Purity | Typically ≥ 98% |
| Flash Point | 155.2°C |
| Storage Conditions | Store in a cool, dry place, tightly closed |
| Chemical Name | 3,4-Dichlorobenzenesulfonyl chloride |
| Synonyms | Benzenesulfonyl chloride, 3,4-dichloro- |
| Hs Code | 29049090 |
As an accredited 3,4-Dichlorobenzenesulfonyl Chloride factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | A 100g quantity of 3,4-Dichlorobenzenesulfonyl Chloride is packaged in a sealed amber glass bottle with a secure screw cap. |
| Shipping | 3,4-Dichlorobenzenesulfonyl Chloride should be shipped in tightly sealed containers, protected from moisture. Transport in accordance with local, national, and international regulations for hazardous materials. Ensure labeling as a corrosive and irritant substance. Store and ship at ambient temperature, away from incompatible chemicals such as water, strong bases, and oxidizing agents. |
| Storage | 3,4-Dichlorobenzenesulfonyl chloride should be stored in a tightly closed container in a cool, dry, and well-ventilated area, away from moisture and incompatible substances such as strong bases and oxidizing agents. Protect from direct sunlight and sources of ignition. Handle under an inert atmosphere if possible. Storage areas should be equipped with spill containment and appropriate safety equipment. |
Applications of 3,4-Dichlorobenzenesulfonyl Chloride in Industrial ManufacturingAs a direct manufacturer of 3,4-Dichlorobenzenesulfonyl Chloride, we supply this key intermediate for specific sectors requiring precise sulfonylation steps or chlorinated aromatic units. Our material meets the quality and consistency demands of high-value downstream applications, supporting both large-scale and specialty production. 1. Pharmaceutical Intermediate SynthesisPharmaceutical API manufacturers incorporate 3,4-Dichlorobenzenesulfonyl Chloride primarily in the preparation of sulfonamide drugs and related advanced intermediates, where the sulfonyl chloride group enables selective functionalization during multi-stage synthesis. Handling, storage, and batch-recording protocols follow sector-specific GMP control to prevent carryovers and ensure traceability. Our plant consistently batches the product to minimize impurities that could compromise downstream API purity or regulatory review, and we offer custom packaging options for aseptic production environments. Industry compliance standards
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2. Agrochemical Active Ingredient ManufacturingIn agrochemical production, formulators use this compound mainly to build sulfonylurea or chlorinated herbicide molecules, selecting it for its reactivity with amines and aromatic substrates. Application-specific batch documentation, emission control, and occupational safety rules strictly govern its handling. Performance consistency with minimal trace metals is vital, especially where downstream crystallization and purification steps demand exacting control to avoid byproducts that may limit field effectiveness or regulatory clearance. Industry compliance standards
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3. Dye Intermediate and Pigment ProductionManufacturers in the dyestuff sector integrate this raw material during the preparation of reactive dyes and specialty pigments, exploiting its dual functionality for introducing reactive sulfonyl and chlorinated groups on aromatic backbones. Strict adherence to environmental discharge regulations and batch-moisture analysis is routine in these plants, as both colorimetric yield and compliance with banned substances listings require precise process control. We supply consistently batched material for minimum foaming and color shade variation in pigment dispersion lines. Industry compliance standards
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4. Polymer Modification and Crosslinker ManufacturingIn the specialty polymer sector, our product sees use for introducing crosslinkable sulfonyl chloride units into engineering resins or as a precursor for high-performance polymer additives. The entry point is tightly controlled to support reproducible polymer branching or functionality enhancement, with quality and purity tracked for each batch under established analytical protocols. Operators monitor dosage through in-situ titration, fine-tuning the ratio for balance between mechanical property improvement and processability, especially in performance film and engineered compound lines. Industry compliance standards
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In our decades at the manufacturing end of the specialty chemicals field, we have learned to value experience over hyperbole. As the manufacturer of 3,4-Dichlorobenzenesulfonyl chloride, our knowledge flows from the factory floor to the customer’s bench, through each lot and every batch that leaves our doors. The market often talks about technical grade specifications or fluorescent data, but as those who design the process, operate the reactors, and control the quality, we know the finer details that impact actual outcomes in application environments.
Our typical manufacturing run of 3,4-Dichlorobenzenesulfonyl chloride (CAS No. 1335-38-2) yields a crystalline solid, usually white to light beige, known for its high purity and stable performance under controlled storage. From our synthesis experience, content regularly measures above 98%, with active chlorine content and low moisture levels maintained to strict standards. This minimizes side reactions, which become apparent during complex sulfonamide synthesis or cross-coupling formation in the pharma and agrochemical industries.
Packaged in lined fiber drums or sealed HDPE containers, we keep product integrity in focus right from crystallization through the last stages of drying and packaging. Particle size distribution aligns with what real users—chemists and formulators—have asked from us: it pours well, handles easily, and disperses with minimal fuss whether your process involves batchwise addition in an organic synthesis vessel or slow dosing over hours to control exotherms. No one wants clumps that break into fine dust just when you need precision dosing.
What most resellers and traders miss is the relationship between process control and the stability of the product over time. As manufacturers, we dedicate a substantial part of our QC routine to trace impurities—not just assay percentages. We monitor for isomers and related sulfonyl chloride analogs that can skew reactivity. 3,4-Dichlorobenzenesulfonyl chloride produces the best results when it contains less than 1% of 2,4-dichloro or 2,5-dichloro positional impurities. Our process chemistry, refined over repeated feedback cycles from end-users, consistently hits such levels.
Our plant teams continually fine-tune reactor temperatures, dosing rates, and workup conditions so that undesired by-products remain at low ppm range. This level of care translates into higher yields when our customers use this material for coupling reactions or derivatizations, especially for pharma intermediates or specialty polymer additives where trace contaminants can poison a catalyst or interfere with a downstream functional group.
Warehousing and shelf life often get overlooked in published spec sheets. As manufacturers, we measure real-world shelf stability, not just the numbers in a data box. Several years ago, customers flagged reactivity losses after exposure to humid conditions. We investigated root causes like residual solvent or trace acid carryover in our drying step, leading the way to adopt vacuum finishing and better container seals. It’s a classic lesson: those closest to production are the fastest to evolve solutions when something hits the end-user.
We also keep hydration and hydrolysis in view: this sulfonyl chloride hydrolyzes gradually on exposure to moist air, generating hydrogen chloride fumes and degrading to sulfonic acid derivatives. Our own labs and pilot teams have tested nitrogen blanketing and low-temperature storage—results show that sealed containers stored in dry, low-light conditions avoid discoloration and greatly prolong reactivity. Guidance we pass to our direct users is built on what our tech crews witness first-hand as substances move through our own warehouse and transit systems, not just what third-party guidelines say.
3,4-Dichlorobenzenesulfonyl chloride serves best when making complex sulfonamide compounds—common in pharmaceuticals, dyes, agricultural active ingredients, and some high-end material polymers. The dual chloro substitution on the aromatic ring at the 3 and 4 positions changes electronic properties vs. mono-chloro or di-chloro isomers placed elsewhere. Direct feedback from pharmaceutical process developers confirms that 3,4-DCBSC often shows better performance in halogenated sulfonamide syntheses, with higher conversion rates and fewer purification cycles, reducing both solvent and time costs.
We’ve worked with fine chemicals companies where the chemistries require strong electrophilic sulfonation with minimal by-product formation. In these scenarios, the 3,4-dichloro isomer outshines less pure or mis-isomerized lots—side products in energetic organic reactions often result from off-spec batches purchased via brokers who miss subtle spectral differences in QC. Full in-house analytics like HPLC, GC-MS, and classic melting point/IR checks from our own QC labs back up each lot shipped.
Polymer researchers and advanced materials scientists come to us for sulfonylation building blocks that allow custom functionalization of aromatic fabrics, membranes, and specialty resins—applications where lower grade sulfonyl chlorides can’t meet performance requirements. We see repeat orders for 3,4-Dichlorobenzenesulfonyl chloride when end-users need compatibility with sensitive cross-linking catalysts or polymer backbones with tight requirement on trace metals and color bodies.
Comparing this compound with generic benzenesulfonyl chloride or other di-chloro isomers shows why our customers insist on specifying not just the product, but the source. 3,4-Dichlorobenzenesulfonyl chloride delivers a specific pattern of electrophilic aromatic substitution, thanks to the 3,4-disubstitution that steers reaction profiles in predictable, repeatable ways. From a manufacturing stance, controlling positional isomerism means careful selection of both starting materials and process controls—an aspect rarely visible outside our quarterly R&D meetings and process reviews.
Go with a cheaper 2,4- or 2,5-dichloro isomer, and you risk poor site-selectivity or hard-to-separate regioisomers in your final synthesis. As the factory, we have the records to show exact origins and process logs instead of just test reports. Bulk intermediates for pharmaceuticals—where cGMP tracking makes or breaks supplier relationships—demand this level of transparency.
Some users report difficulties dissolving ill-prepared lots or seeing yield loss due to inconsistent melting points. Both relate to small but significant variations during final drying under vacuum—an aspect our own operations team spent several quarters tuning. We share best-practice guidance about slow, controlled addition to reaction media to avoid local overheating or uncontrolled HCl evolution, because we’ve traced customer complaints about foaming and side reactions back to improper compounding and lack of direct communication from brokers who lack hands-on process feedback.
Quality doesn’t just start at the reactor; it follows through in how a manufacturer handles post-production packaging, internal labeling, and traceability. Over the years, several bulk buyers have come back to us with gratitude, not because the product was always perfect, but because our production logs and analytical data helped their own RCA process when something unexpectedly went awry in their plant.
Our production experience shows that even the best preparations of 3,4-Dichlorobenzenesulfonyl chloride need robust handling and storage. The chemistry behind reactive sulfonyl chlorides—especially those bearing aryl dihalides—means any moisture, excess heat, or sunlight poses a real threat to stability and purity. To handle this, we monitor storage room conditions, regularly rotate drums, and work closely with shipping teams to minimize temperature excursions during hot and humid months.
Once, during a particularly humid summer, we found increased trace hydrolysis in stock material despite sealed packaging. Root cause analysis led to an upgrade in drum liner specifications and revised humidity controls across our warehouse. As producers, these real-world improvements trickle down directly to benefits for our customers—longer shelf life, less batch-to-batch variability, and more predictable reactivity.
OEM manufacturers, academic researchers, and toll processors have taught us that no spec sheet fully replaces direct conversations about process idiosyncrasies. More than once, we discovered that what looked like a rare impurity only became problematic at scales of several hundred kilos, or only after a particular synthesis cycle in an international customer’s plant. We take those learnings back into the next campaign—in-process analytics, additional filtration steps, or upgraded packaging—and the next batch reflects those changes.
Our scale-up engineers and chemists build what we know from every plant run. If a customer using 3,4-Dichlorobenzenesulfonyl chloride for diazotization sees a specific trace impurity in their HPLC, we can refer right back to in-process checks. Over time, this has helped us refine both our own crude isolation steps and the maintenance routines on distillation gear to avoid back-migration of certain volatile byproducts.
We see environmental and regulatory standards moving targets. Modern customers demand lower residual chlorinated species and minimized by-product waste both for worker safety and for compliance reasons. Our own in-house EHS team regularly upgrades process controls, like improved vent scrubbing, tighter process monitoring, or redesigned workups to recover unreacted starting material. These changes may not show up on a material datasheet, but they matter for supply chain integrity, user safety, and environmental impact.
As producers, we go beyond regionally required limits for packing and shipping hazardous goods, training handlers and drivers to understand product risks, and pre-advising customers about best storage conditions in their local environment. We participate in audits and partner with users to reduce single-use plastics and develop returnable drum options where safe and feasible, sharing both environmental and economic benefits through the supply chain.
End-users rarely ask about academic literature values on minor impurities or hypothetical degradation pathways. Instead, the questions are practical: How does this batch behave in a scaled-up Mannich reaction? What’s the long-term stability after six months in bulk storage? Will your lot handle the stress of pressure transfer in automated lines? Our plant and tech teams answer these with years of practice, tracked through batch consistency and actual trouble-shooting reports.
Sharing our process data and lessons learned, instead of relying on distributor claims, builds the trust that direct buyers look for. Whether current customers use our 3,4-Dichlorobenzenesulfonyl chloride for sulfonamide couplings, as a lab reagent, or as an industrial-scale feedstock, they appreciate the ability to get information directly from those who have run the reactors and lived through both successes and rare failures.
True innovation in this sector often means incremental improvements—a change in the recrystallization slurry rate, a tweak to reaction solvent, or hours spent optimizing filtration and final drying. Being on the manufacturing side lets us move quickly on improvements based on our own or customer feedback, not wait for permission from a procurement department buffered by layers of distribution.
An example from recent years: adapting to a customer’s new continuous-flow synthesis, we modified our particle size and bulk density protocols so the product would feed smoothly into closed line systems. Our in-house QA team responded by updating grade specifications, and our process group verified compatibility by running parallel tests in our pilot reactors. These refinements don’t appear in standard product blurbs but reflect real partnership and responsiveness only a dedicated chemical maker can offer.
The knowledge we share here is built from decades of hands-on production, technical problem-solving, and honest interaction with everyone in the chain from plant operator to end chemist. 3,4-Dichlorobenzenesulfonyl chloride has earned its reputation through actual performance in synthesis, by meeting demanding purity, stability, and application targets—not from generic copy or trading-room claims.
Every kilogram is the sum of thousands of pilot and commercial-scale runs, process reviews, customer phone calls, and technical investigation. Each new season or shift brings further tweaks and improvements. As manufacturers, we value straight communication and operational expertise, offering our direct real-world perspective and manufacturing know-how to help customers achieve the results they expect—and often better.