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HS Code |
317279 |
| Product Name | 4-Chloro-2-Fluorobenzenesulfonyl Chloride |
| Cas Number | 64116-59-6 |
| Molecular Formula | C6H3Cl2FO2S |
| Molecular Weight | 229.06 g/mol |
| Appearance | White to off-white solid |
| Purity | Typically ≥98% |
| Melting Point | 50-54°C |
| Solubility | Reacts with water, soluble in organic solvents |
| Storage Condition | Store in a cool, dry place; keep container tightly closed |
| Hazard Class | Corrosive, irritant |
| Smiles | C1=CC(=C(C=C1S(=O)(=O)Cl)Cl)F |
As an accredited 4-Chloro-2-Fluorobenzenesulfonyl Chloride factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | A 250g amber glass bottle with a sealed cap, labeled "4-Chloro-2-Fluorobenzenesulfonyl Chloride," hazard warnings, and handling instructions. |
| Shipping | 4-Chloro-2-Fluorobenzenesulfonyl Chloride is shipped in tightly sealed containers, protected from moisture and sunlight. Classified as a corrosive and irritant substance, it is handled according to hazardous materials regulations. Packaging adheres to UN safety guidelines, with appropriate labeling for chemical hazards and required documentation for transport by air, sea, or land. |
| Storage | 4-Chloro-2-Fluorobenzenesulfonyl Chloride should be stored in a cool, dry, and well-ventilated area, away from direct sunlight, heat sources, and incompatible substances such as water, alcohols, and bases. Keep the container tightly closed, using corrosion-resistant materials. Store under inert atmosphere if possible. Appropriate chemical-resistant secondary containment is recommended to prevent spills or leaks. |
Applications of 4-Chloro-2-Fluorobenzenesulfonyl Chloride in Industrial ManufacturingAs a direct manufacturer specializing in sulfonyl chloride derivatives, we supply 4-Chloro-2-Fluorobenzenesulfonyl Chloride for established downstream applications where precise reactivity and high assay levels are essential. Below, we detail its specific roles within core chemical manufacturing sectors, highlighting process integration, composition ratios, compliance references, and finished goods produced by our clients worldwide. 1. Agrochemical Synthesis: Sulfonamide Herbicide IntermediateLeading agrochemical formulators use this intermediate to construct targeted sulfonamide herbicides by introducing the sulfonyl chloride group into aromatic rings, improving herbicidal spectrum and environmental stability. This integration creates active moieties with selectivity for broadleaf and grassy weed control, meeting strict residue and toxicological specifications required for modern crop protection solutions. Industry compliance standards
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2. Pharmaceutical Manufacturing: Key Intermediate for Antibacterial APIsAPI manufacturers incorporate this sulfonyl chloride for the synthesis of second-generation sulfonamide antibiotics and other benzene sulfonamide class compounds. The selective mono-chloro/fluoro functionalization enables downstream coupling with amine pharmacophores, used in both pilot and commercial medicinal chemistry production chains under controlled cGMP conditions. Industry compliance standards
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3. Specialty Polymer Modification: Functional Polymer Cross-LinkerEngineered polymers and resins benefit from controlled introduction of sulfonyl chloride groups using this compound as a cross-linking agent, which confers unique electronic or chemical resistance attributes. Industry leaders in high-performance coatings, membranes, and electronic encapsulants rely on it for precise molecular weight distribution control during polymer backbone modification. Industry compliance standards
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4. Advanced Dye and Pigment Manufacturing: Reactive Sulfonylating AgentLeading dye and pigment producers employ this compound as a reactive sulfonyl source for synthesizing water- and solvent-soluble azo and anthraquinone colorants. The functionalization improves fastness properties and dye-substrate bonding for applications in technical textiles, printing inks, and specialty pigment dispersions, requiring strict compliance to safety and environmental standards. Industry compliance standards
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5. Electronic Chemicals: Semiconductor Etchant and Photoresist SynthesisSemiconductor material producers and photoresist formulators utilize this compound to introduce specific sulfonyl fluorinated functionalities that deliver etch resistance and precise pattern definition in microfabrication chemicals. Consistent high-purity lots and trace metal analyses are critical for integration into strict contamination-controlled production workflows. Industry compliance standards
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On our plant floor, every batch of 4-Chloro-2-Fluorobenzenesulfonyl Chloride reveals something new — careful reactivity, unwavering structure, and potential for synthesis rarely matched by similar sulfonyl chloride intermediates. The molecular profile includes a targeted placement of both chlorine and fluorine atoms on the aromatic ring. This arrangement sets off a unique reactivity, particularly for active pharmaceutical ingredient manufacturing and advanced material synthesis.
Outsiders might not realize how much practical know-how goes into converting this intermediate into a reliable, high-quality product. The model we follow, often referenced by its CAS number 59792-27-5, has roots in reaction monitoring that goes beyond simple analytical checks. Maintaining a consistent appearance, white crystalline powder or pale crystals, we focus on minimizing moisture absorption from the air, which can otherwise lead to corrosive byproducts and off-ratio formulations. This attention pays off for clients who want purity and stability right where it matters most.
Like other sulfonyl chlorides, this product finds use as a synthon in pharmaceuticals and agrochemical projects. Still, minor shifts in the molecule make an outsize difference. The para-chlorine and ortho-fluorine substitution pattern, unlike traditional benzenesulfonyl chlorides, supports selective coupling and ring formation routes that improve downstream synthetic control. Our observation has been that the double halogen pattern often delivers better separation between the compound and impurity streams, cutting purification times for customers who run several pilot reactions at commercial scale.
With melting points typically in the high double digits Celsius, storage needs less refrigeration than more volatile acyl halides. The heavier atom substitutions drive stronger intermolecular packing, so product lumps less easily in transit or storage, even under humid conditions across seasons. These physical gains reduce waste and cleaning downtime in high-throughput reactors.
We have lost count of how many times a minor impurity shows up in downstream analytics, only to trace it back to a sloppy dehydration or exposure to air during our own initial batch work. By now, repeat testing on each drum, with extra GC-MS runs for every production lot, has become second nature. Over the years, we've honed the chlorosulfonation and halogen-exchange reactions to minimize side product formation. The use of anhydrous conditions and strictly monitored chlorinating agents matters far more than generic instruction sheets promise.
No two synthesis routes produce identical impurity fingerprints, especially if scale is ramped up rapidly. With 4-Chloro-2-Fluorobenzenesulfonyl Chloride, pressure control and quenching parameters need constant attention or hydrolysis can spike, destroying key intermediates for active substance preparation. Unlike benzenesulfonyl chloride or mono-chloro analogues, this product reacts faster with amines and alcohols in coupling steps. Our teams notice sharper endpoint transitions, which helps process engineers minimize overreaction and unwanted bi-products.
Our engineers run the process reactors under nitrogen blankets, pushing for trace-level control of water vapor. In one building, custom scraper-type filters reduce particle carryover from each batch, so our customers downstream avoid filter fouling. When bottling the final product, we use inert gas for flushing, which our analytics group finds preserves stability for shipping across varying climates.
Over the years, we’ve adjusted packaging from the basic fiber drums to multilayer foil composites. Single-layer packaging looked like enough for routine handling, yet container fouling and occasional caking appeared in long-haul shipments. With more robust packaging, users report fewer clumps and less need to rescreen before dissolving the material for reactions. Quality gains are real, and they cut hidden costs for fellow chemists at the receiver’s end.
The familiarity with real-world factory cycles leads us away from fanfare and straight to raw benefits. A solid batch of this sulfonyl chloride outperforms close relatives, such as 2-Fluorobenzenesulfonyl chloride or 4-Chlorobenzenesulfonyl chloride, in multi-step synthesis. The electron-withdrawing pattern brings control in nucleophilic aromatic substitution and specialized arylation, a detail appreciated by process R&D teams who speak our language.
This intermediate acts as a foundation for sulfonamide assembly, especially where selective activity is needed at the aryl ring. Active ingredient research teams draw on these substitution patterns to set precise biological activity. For example, the dual halide arrangement on our molecule curves the electronics in medicinal chemistry, opening paths closed to single-halide benzenesulfonyl chlorides. In fieldwork, agricultural chemistry partners use it as a core for herbicide or fungicide development, where substitutions at C2 and C4 allow custom-tailored action spectra.
Beyond pharma and agro, electronics companies come to us for advanced polymer synthesis. Many newer specialty polymers feature sulfonyl chloride intermediates for building block attachment. When our customers craft high-performance ion-exchange membranes or custom advanced coatings, the site-directed halogen pattern means tighter control over substitution ratios and fewer byproducts after post-chlorination or sulfonylation steps.
Across many test runs and seasonal production batches, our team studies how minor temperature and humidity swings change the properties of each finished lot. This vigilance keeps off-spec material from entering our customer pipelines and shields their process lines from downtime.
No single chemistry matters more than safe handling. Over the years, we’ve seen where tight control over packaging integrations keeps reactive fumes contained and prevents accidental contact. Teams across the floor train on handling procedures developed through tough lessons and sustained improvement cycles.
Even at expert hands, sulfonyl chlorides demand respect for their reactivity with water. That’s why dry, ventilated storage, tools rated for aggressive halogenation work, and protective gear never get skipped. Collaborative work with downstream users brings up potential interaction scenarios—whether it’s during pilot runs for new pairings with sophisticated electronic substrates or on the line for bulk pharmaceutical reprocessing.
Beyond printed safety data, real practice defines which routines cut risk. Staff members triple-check moisture barriers and handle transfers only in well-ventilated areas. We see less downtime, smoother customer production, and fewer emergency logs as a result.
Process teams sometimes begin with plain benzenesulfonyl chloride as a baseline. Our product, by integrating chlorine and fluorine at precise positions, gives them leverage for exclusive bond formation. While 2-Fluorobenzenesulfonyl chloride helps with certain substitutions, our 4-Chloro-2-Fluorobenzenesulfonyl Chloride shifts reaction equilibrium, boosting yield in challenging sulfonamide syntheses.
For research groups in pharmaceuticals or materials chemistry, the greater electron deficiency means nucleophilic displacement steps go cleaner and faster. We’ve watched purification steps for some analogues drag on, only to see breakthroughs with our compound, which leaves behind purer side streams and lowers the load on waste processing equipment. The long-term benefit stretches beyond one reaction — every stage, from preparation to work-up, carries simplified cleanup and analytical checks.
Compared to less substituted sulfonyl chlorides, our compound’s melting point helps it ride longer shipping routes without turning sticky or giving off fumes under minor heat. Packing and storage teams report lower off-gassing rates, leading to reduced loss and more reliable shipments. Fewer surprises at customer handling sites mean stronger production partnerships and less troubleshooting at the receiving dock.
The pressure to scale up often puts both people and protocols on edge. Our transition from kilo-scale to ton-scale production uncovered that even slightly stale chlorinating agents leave behind stubborn impurities, resistant to normal batch washes. Years of process tweaks focused us back to raw material sources: freshness, consistency, trace analysis, and cooperative record-sharing with supply partners.
Many upstart producers overlook subtle downstream impacts. Even a 0.1% impurity in our sulfonyl chloride carries downstream, roughing up spectral data and muddying bioprocess screens. We adopted redundancy in our analytical checks for just this reason. Real production means each lot, each shift, gets verified by both classic titration and modern chromatography. Staff calibrate against in-house standards regularly, and client audits—sometimes unannounced—keep our vigilance sharp.
It’s one thing to claim a specification on paper. The world of chemical manufacturing revolves around details that don’t always make it onto a technical data sheet. With project-based feedback from both multinational drug developers and lean startup labs, we sync our practices to what actually happens in the field. For every order, direct questions come back: What was the last temperature the batch saw? How quickly after capping did packing start? Seasoned clients see the difference in their product yields and troubleshooting frequencies.
Practically, that means we anticipate peaks in temperature and humidity, adjust workflows for faster sealing, and even tweak batch sizes to keep lead times short. Over time, this reduces mis-labeling mishaps, stops reactive byproducts from sneaking in, and makes each consignment easier to track for regulatory inquiries.
Through years of hands-on adjustments and customer demand, traceability became both a legal and quality imperative. Each batch receives a digital chain of custody that links it to storage and production parameters, as well as shipping conditions. Purchasers often ask for information down to the last storage tag in the warehouse, and our systems answer these questions on demand.
Close collaboration with our analytics lab led to daily SOP fine-tuning. Every employee, from floor operator to logistics, knows the direct impact of even a slight slip in drying or capping rates. We saw finished lots rejected at the customer’s scale-up stage just from ambient humidity spikes during the fill process. These kinds of feedback loops forced better laboratory automation, regular retraining, and stricter batch-by-batch analysis, feeding lessons directly into the next run.
Handling sulfonyl chlorides responsibly extends far past product completion. Across the factory site, dedicated waste treatment lines handle any hydrolyzed byproduct streams. Monitoring and recycling solvents at scale cut both raw material usage and off-plant emissions. Community transparency on waste processing gains trust with local authorities and workers alike.
We see sharper focus from partners about environmental impacts at every point. Increasingly, buyers look for a trail of responsible sourcing, solvent minimization, and emissions data. Integrating internal recycling of spent solvents means not just regulatory compliance, but lower costs and open pathways for long-term contracts with sustainability-minded customers.
Routine customer site visits and audits have shown where our product behavior deviates in end-use reactors or production lines. We adjust shipping methods, improve vacuum-tight seals, or switch batch cycling times based on data surfaced from these cross-company exchanges. In one case study, a customer's polymerization sequence produced an unexpected haze traced back to micro-trace solvent residue. Joint review with their technical team resulted in modified post-wash cycles from our side — an upgrade now standard for future shipments.
Several research clients value not only the compound itself, but the insight that comes from our collective failure analysis and troubleshooting. For applications in precise drug screening or catalytic materials, minute differences in sulfonyl chloride purity tip the balance toward successful project milestones. Seasoned staffers remain reachable for direct feedback, adjusting practices that too often remain static in larger, less engaged chemical enterprises.
Building trust in each drum and each report means sharing not just numbers, but also the narratives of continuous improvement and error correction.
As product demand swings toward higher purity and near-zero residue mid-stage intermediates, we keep watching and adapting. New pilot plants on site let us run quick turnarounds on alternate synthetic routes, stress-test product under different humidity and storage conditions, and bring on-the-ground learnings back to the main lines. Changes in global supply chains – whether delayed shipments or raw material shortages – push us to optimize suppliers, diversify sourcing, and build more resilience in our own systems.
We believe it’s not enough to deliver a set of specification numbers. The value of 4-Chloro-2-Fluorobenzenesulfonyl Chloride is validated each time it passes smoothly from shipping drum to reaction flask, performing as expected in the hands of those who build breakthrough molecules and materials. The lessons we have drawn, batch after batch, offer an experience that a simple technical bulletin cannot communicate, but one that our partners recognize in their own yields and timelines.