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HS Code |
583164 |
| Product Name | 2-Chloro-4,5-Difluorobenzenesulfonyl Chloride |
| Cas Number | 387863-80-7 |
| Molecular Formula | C6H2ClF2O2SCl |
| Molecular Weight | 247.55 g/mol |
| Appearance | White to off-white crystalline solid |
| Purity | Typically >98% |
| Melting Point | 54-58°C |
| Density | 1.68 g/cm³ (approximate) |
| Solubility | Reacts with water; soluble in organic solvents such as dichloromethane |
| Storage Conditions | Store in a cool, dry place, tightly closed, under inert atmosphere |
| Hazard Codes | Corrosive |
| Smiles | C1=C(C(=C(C=C1S(=O)(=O)Cl)F)Cl)F |
| Inchi | InChI=1S/C6H2Cl2F2O2S/c7-3-1-4(9)6(13(8,11)12)5(10)2-3/h1-2H |
As an accredited 2-Chloro-4,5-Difluorobenzenesulfonyl Chloride factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 500g of 2-Chloro-4,5-Difluorobenzenesulfonyl Chloride is supplied in a tightly sealed amber glass bottle with hazard labeling. |
| Shipping | 2-Chloro-4,5-Difluorobenzenesulfonyl Chloride should be shipped in tightly sealed containers, clearly labeled, and protected from moisture and heat. As a corrosive and potentially hazardous chemical, it must be handled according to local regulations, using appropriate packaging (such as UN-approved containers) and accompanied by necessary safety and shipping documentation. |
| Storage | Store 2-Chloro-4,5-difluorobenzenesulfonyl chloride in a cool, dry, and well-ventilated area, away from direct sunlight and moisture. Keep the container tightly sealed and segregated from incompatible materials such as water, alcohols, amines, bases, and strong oxidizers. Use a corrosion-resistant container and clearly label it. Handle under an inert atmosphere if possible, and avoid inhalation or contact with skin and eyes. |
Applications of 2-Chloro-4,5-Difluorobenzenesulfonyl Chloride in Industrial ManufacturingAs the manufacturer of 2-Chloro-4,5-Difluorobenzenesulfonyl Chloride, we support downstream industrial partners in multiple advanced chemical sectors where precision and compliance drive material selection. The following application scenarios represent the actual deployment of this intermediate in specialized production environments. 1. Agrochemical Synthesis: Sulfonylurea Herbicide IntermediateCrop protection product manufacturers incorporate this sulfonyl chloride derivative as a key sulfonylation agent in synthesizing sulfonylurea herbicides. Its reactivity allows controlled introduction of the sulfonyl chloride group, creating herbicide actives with target-specific weed control properties. This step requires careful process management to maintain both yields and downstream purity necessary for formulation. Industry compliance standards
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2. Pharmaceutical Manufacturing: Advanced API IntermediateAPI manufacturers select this building block for producing fluorinated and chlorinated aromatic sulfonamides, which serve as key scaffolds in anti-inflammatory and oncology drug pipelines. Its precise reactivity profile enables site-selective functionalization of aromatic rings, resulting in superior purities and fewer side reactions compared to less substituted analogs. Industry compliance standards
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3. Specialty Polymer Modifier: High-Performance Fluorinated CopolymersProducers of specialty polymers and advanced composites employ this sulfonyl chloride as a reactive chain modifier to introduce electron-withdrawing substituents, improving resistance to solvents and thermal degradation. The chemical structure enables fine-tuning of polymer backbone properties in applications ranging from proton exchange membranes for fuel cells to dielectrics in electronics. Industry compliance standards
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4. Fine Chemical Sulfonation Agent: Custom Fluorinated Aromatic CompoundsContract manufacturers and custom synthesis operations use this sulfonyl chloride as a sulfonation agent in elaborating fluorinated benzene derivatives for research, photonics, and advanced material sectors. Its selective reactivity in the presence of multiple halogens allows precise insertion of sulfonyl functionalities into complex molecular architectures. Industry compliance standards
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5. Active Ingredient for Industrial BiocidesIndustrial formulators select this material as a precursor for high-performance fluorinated arylsulfonamides, incorporated into biocidal mixtures targeting microbial contamination in paints, coatings, and water treatment systems. The compound’s unique substitution pattern imparts strong biological activity while enabling compatibility with diverse formulation chemistries. Industry compliance standards
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Working from decades inside our own production floors, we've developed a close relationship with the demands that 2-Chloro-4,5-Difluorobenzenesulfonyl Chloride brings to the table. This compound, with its unique structure—ringed by both chlorine and fluorine substitutions—serves as a backbone for tough, high-purity applications, especially in pharmaceuticals and advanced materials. Many customers often ask about its model number, but our focus has always rested more on consistency and performance metrics than catchy labels.
Since we oversee every stage from raw material sourcing to final QC, we have tightened our process controls to minimize batch deviation. With our reactors set up for both high-throughput and traceable batch sizing, we track parameters like residual moisture, active content, and color index for every lot. Customers often seek this transparency, wanting to know how a given batch will perform two years after manufacture or how it will behave in extra-sensitive downstream steps. In these cases, logic trumps theory—the fewer surprises in their feedstocks, the less risk of costly delays.
At face value, 2-Chloro-4,5-Difluorobenzenesulfonyl Chloride might look similar to other sulfonyl chlorides, but the detail lies in the fluorine and chlorine positioning along the aromatic ring. Fluorine is notorious for toggling both chemical reactivity and metabolic stability. Chlorine, known for its effects on leaving-group quality, opens up pathways unavailable to plain benzenesulfonyl chloride. What our clients witness—especially those in pharmaceutical synthesis—is that these halogen substitutions let them build target molecules that would otherwise take more steps, cost more, and produce more waste.
We’ve seen this product provide sharper yields and cleaner profiles when forming sulfonamide bonds, particularly with heterocyclic amines. Many generic sulfonyl chlorides generate a broader impurity spectrum; this specific molecule, because of its electron-rich and electron-withdrawing mix, often reacts under milder conditions with less catalyst load. Over a thousand kilo-scale reactions later, our team fully appreciates how these differences show up in the actual plant. Several industrial chemists tell us they see better downstream filtration, less color pickup, and more predictable assay results with our 2-Chloro-4,5-Difluorobenzenesulfonyl Chloride compared to single-halide or unsubstituted variants.
Beyond textbook reactions, the way our product gets used says more about its value than any theoretical summary. In crop protection, manufacturers turn to this sulfonyl chloride for precise introduction of sulfonamide functions, a key scaffold for herbicides that require both durability in sunlight and robust selectivity. Several dye and pigment makers have turned to this molecule to introduce unique chromophores that demonstrate higher stability under both acid and alkali textile processes.
Pharma customers approach us with increasingly complex starting materials, and 2-Chloro-4,5-Difluorobenzenesulfonyl Chloride supports routes to kinase inhibitors and anti-infective agents requiring site-specific coupling. Compared to softer analogs, our product resists hydrolysis better during prolonged reactions, meaning less loss and fewer purification headaches.
In our own packing and transfer, we’ve experienced firsthand how this sulfonyl chloride’s volatility and moisture sensitivity put pressure on handling systems. Compared to mono-halogenated versions, the difluoro-chloro pattern creates a slightly lower melting point and enhanced reactivity. We pay extra attention to inert-gas blanketing and vapor containment during charging—hard lessons learned from long nights cleaning up crystallized residues from early production campaigns.
Storage conditions create a ripple effect on shelf life and purity. Over the years, our facility has moved from atmospheric storage to sealed, nitrogen-flushed containers, preserving the product's clarity and reducing decomposition byproducts. Pouring it directly in jacketed lines, we avoid heat excursions that can spike impurity formation. These changes came out of running hundreds of full-sized tanks, not from theory.
Modern downstream syntheses require more than an “on-spec” product sheet. Labs and plants today deal with regulatory filings where even minor unknowns can derail a commercial launch. Our analytical chemists run GC and HPLC checks on every lot, measuring byproducts below 0.05% threshold. We’ve found that high-resolution NMR often flags trace contaminants missed by quick spot tests, avoiding surprises in large-scale production. Customers don’t need to ask for this; we've made it standard because sitting in joint development meetings with their R&D teams showed us the value of being able to trace a batch back to the minute it left the reactor.
The extra halogen content also increases the product’s mass balance sensitivity. Minor changes in drying, even a three-degree shift or short stoppage, can swing the purity specs visibly. That's why site engineers stay close to each vessel, logging each transfer and routinely testing after every blend, not just after the batch is supposed to be done. From our experience, that hands-on approach leads to less variation over time, which end users confirm in their own validation runs.
Several buyers have asked why one should pick 2-Chloro-4,5-Difluorobenzenesulfonyl Chloride over the more common p-toluenesulfonyl or plain benzenesulfonyl chloride. We've run the numbers on this in head-to-head campaigns. For one, the electron-demanding fluoro-chloro framework gives more controlled kinetics in nucleophilic substitution reactions. This translates to more substrate being converted before side reactions eat into the yield, and less aggressive work-up conditions that can damage sensitive core structures. From a regulatory standpoint, decreased side product generation means a faster analytical clearance for pharma launches.
Manufacturers in agrochemicals have found fewer residuals in formulation when switching to this compound; the residual profile is cleaner, with less bleed-through into formulated products. Energy savings also add up: milder reaction conditions supported by the unique halogen pattern let reactors run at lower temperatures, which over the years has translated directly into savings on utility bills and less environmental load.
Scaling from lab to plant reveals quirks—something no spreadsheet or bench-top pilot can truly forecast. In our earliest years manufacturing this product, we encountered batch-to-batch vapor losses and clogging inside condenser traps. In one instance, our QC flagged off-color residues indicating trace hydrolysis. Instead of adjusting specs downward, we reinforced all transfer connections and instituted a rapid-cooling step right after reaction completion. It meant retooling the plant for this specific product, but customer complaints stopped, and stability improved across shipments.
Over multiple campaigns, we also tackled dusting during powder discharge, an occupational risk that’s easy to ignore in small volume but can cost dearly at scale. Local exhaust upgrades and covered feed chutes made this product easier and safer for our operators—a choice reflecting more than compliance. By addressing these process risks through site investments, we reduced downtime and ensured the integrity of every batch heading to customer sites.
The main value our clients get isn't simply a drum or bag filled with chemical—it’s the peace of mind that their next production window won’t be lost to off-batch reactivity or impurity spikes. Pharmaceutical accounts report better control over API step yieds and fewer purification cycles. Agrochemical makers tell us about shorter campaign times and less regulatory paperwork tracing unexpected by-products.
End users working on research scale often come back years later with new, larger contracts. That’s happened because our product performs the same at 10 grams as it does at 500 kilos: the fingerprint spectra match, impurities don’t creep up, and logistics are as reliable as the chemistry. Supply chain managers trust that if we commit to a timeline, we’ll either hit it or warn them early enough to adjust their plans. That underpins so much of the relationship beyond price per kilo.
Supply interruptions sometimes happen for raw halides or precursor fluorinated aromatics, but by building redundancy into our upstream vendor base and maintaining local reserves, we hedge against loses that could otherwise cascade down into customer production lines. We share forward planning data with our biggest clients, letting us forecast volume spikes and trigger early procurement of critical raw materials.
Downstream, we offer optional co-development on process improvements, including custom particle sizing or targeted drying profiles. Over one recent campaign, a client specializing in battery electrode materials needed tighter spec controls on residual chloride. We worked through two production trials to recalibrate our drying and controlled-atmosphere storage; their next batch met both specification and production timing without extra cost on either side.
Modern manufacturing calls for more than just hitting potency numbers. Over the years, our plants adopted closed-loop emission capture and aggressive solvent recycling, not just because we needed to—because we frankly didn’t want to face downstream waste headaches for ourselves or for our customers. Sulfonyl chlorides, in general, carry a reputation for challenging waste streams. Our on-site treatment systems strip out residual chlorides before aqueous discharges leave our fence line. Quarterly environmental audits validate actual downstream discharge against internal standards set tighter than most local agencies require.
By optimizing reaction temperatures and recycle rates on solvents like dichloromethane or acetonitrile, we have ratcheted down both off-gas and hazardous waste output. Some of these upgrades pay for themselves in under a year through material savings alone. In the long run, we’ve learned that running a plant cleanly means we own our mistakes faster, solve problems upfront, and keep community trust.
Developing a new drug candidate or specialty agrochemical often puts teams under pressure to document trace impurity levels and batch genealogy. Our staff fields direct requests for sample archiving, CoA customizations, and method validation packages so that senior scientists at client sites can get investigations closed quicker. Our regulatory support team draws on lab and production background, not just document-clerking—real support that has helped launch multiple new entities using this exact chemical backbone.
We partner in stability studies for long-haul logistics and atypical storage conditions. One multinational requested six-month, high-temp stability checks after cargo delays exposed their shipment to 45°C. Our product retained both assay and color—rooted in a production approach geared toward minimizing labile byproducts before shipment.
Problems rarely surface on Day One of a campaign. Usually, quirks reveal themselves after months in storage or when a new downstream reagent comes into play. We keep open logs between our QC and customer tech teams, sharing anomaly reports and running parallel checks if someone spots an off note in downstream syntheses. This transparency has shifted complaint investigations from defensive posturing to joint problem solving—resulting in improved specs or modified storage, not just apologies or rebates.
Our technical reps log on-site visits and follow-up calls as tools for continual improvement, not paper compliance. These exchanges have improved both internal process controls and customer experience, delivering better yield consistency and reducing inbound support requests over time.
Producing 2-Chloro-4,5-Difluorobenzenesulfonyl Chloride at industrial volumes, we've come to recognize that reliability outperforms theory. Physical details matter: batch temperature, air quality, cleaning contact times, and tank turnover frequency. Our own workforce walks the sites, eyes on the gauges, and hands on the valves—learning and re-learning what it takes to make the grade batch after batch.
Ultimately, choosing this sulfonyl chloride comes down to control—both in chemical terms and in the predictability of supply, communication, and technical backup. Clients who’ve weathered urgent production challenges with us return because of these realities, not because of some abstract advantage. We commit to this level of service because we know the stakes: clockwork chemistry around the world, built on a bedrock of reliability in a single chemical plant.