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HS Code |
469105 |
| Chemical Name | (4-Fluoro-Phenyl)-Methanesulfonyl Chloride |
| Cas Number | 87874-24-2 |
| Molecular Formula | C7H6ClFO2S |
| Molecular Weight | 208.64 |
| Appearance | White to off-white solid |
| Melting Point | 46-48°C |
| Solubility | Reacts with water; soluble in organic solvents |
| Purity | Typically ≥98% |
| Smiles | CS(=O)(=O)Cl |
| Synonyms | 4-Fluorobenzenemethanesulfonyl chloride |
| Hazard Statements | Corrosive, may cause burns |
As an accredited (4-Fluoro-Phenyl)-Methanesulfonyl Chloride factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 250g of (4-Fluoro-Phenyl)-Methanesulfonyl Chloride supplied in a sealed amber glass bottle with hazard labeling and tamper-evident cap. |
| Shipping | (4-Fluoro-Phenyl)-Methanesulfonyl Chloride is shipped in secure, airtight containers to prevent moisture and air exposure. Packaging complies with chemical safety regulations, including labeling and hazard documentation. The shipment is handled as a corrosive substance, requiring appropriate protective measures and temperature control during transit. Ensure compliance with all local and international transport regulations. |
| Storage | (4-Fluorophenyl)methanesulfonyl chloride should be stored in a cool, dry, and well-ventilated area, away from moisture, heat sources, and incompatible substances such as strong bases and oxidizers. Keep the container tightly closed and protected from direct sunlight. Store in a corrosive-resistant container with appropriate secondary containment. Ensure proper labeling and restrict access to authorized personnel only. |
Applications of (4-Fluoro-Phenyl)-Methanesulfonyl Chloride in Industrial ManufacturingAs the original manufacturer, we supply (4-Fluoro-Phenyl)-Methanesulfonyl Chloride to global B2B clients for specialized synthesis across pharmaceutical, crop protection, and advanced material applications. Our product supports industrial-scale formulations where specific sulfonylation and fluorinated aromatic intermediates deliver targeted properties and downstream efficiency. Below, we detail the principal application areas with relevant technical, regulatory, and production criteria. 1. Pharmaceutical Intermediate SynthesisMajor pharmaceutical producers use this sulfonyl chloride as a selectivity enhancer in active pharmaceutical ingredient (API) synthesis targeting anti-cancer and anti-inflammatory compounds. It reacts in late-stage sulfonylation to introduce unique aromatic functionality, directly influencing purity, bioavailability, and final yield. Integration occurs in multi-step GMP route synthesis, often employing chlorination or coupling reactions under inert atmospheres. Industry compliance standards
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2. Agrochemical Synthesis (Herbicide Intermediate)Crop protection manufacturers use this specialty chlorine donor in selective sulfonylurea and triazine herbicide pathways. Its integration enables efficient formation of fluorinated aromatic rings, conferring stability against UV degradation and contributing to target selectivity in the field. Controlled addition ensures regulatory-compliant residue profiles in the final agrochemical. Industry compliance standards
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3. Specialty Polymer Monomer ManufacturingAdvanced materials producers incorporate this reactive chloride in the synthesis of high-performance monomers for fluorinated poly(arylene sulfone) polymers. Its role centers on controlled introduction of sulfonyl groups, critical for mechanical strength and chemical resistance in end-use membranes and coatings. Stringent process controls ensure high molecular weight build-up and minimal residual chloride. Industry compliance standards
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4. API Impurity Profiling Reagent SupplyPharmaceutical analytical laboratories use this specialty chloride as a certified standard to prepare process impurity benchmarks during new API route development and regulatory filing. Its chemical identity supports trace-level quantification of process-related sulfonylated impurities, underpinning ICH Q3A/Q3B compliance in finished drug substances and products. Industry compliance standards
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Day after day in our plant, the rhythm of synthesis stays steady. With (4-Fluoro-Phenyl)-Methanesulfonyl Chloride, experience has taught us that repeatability matters the most. We run dedicated reactor trains to keep batches consistent, minimize cross-contamination, and achieve a product with high purity. Our production process starts with phenylmethanesulfonyl chloride, then introduces a selective fluorination step. The resulting compound, CAS 351003-08-6, has established itself as a cornerstone in sulfonylation chemistry.
This molecule serves teams in pharmaceuticals, agrochemicals, and advanced materials. It doesn’t just pad out catalogs or sit in warehouses. Researchers leverage its reactivity in sulfonylation reactions. We hear from process chemists who convert amines, alcohols, or heteroaromatics using our sulfonyl chloride, often while chasing new patent spaces or streamlining downstream steps. The 4-fluoro substituent offers strong electron-withdrawing character, setting it apart from plain benzenesulfonyl chloride or even the 4-methyl variant, making it a preferred coupling partner where activation is critical.
Adding a fluorine atom changes reaction profiles. We manufacture this compound to meet the needs of teams requiring precise SN2 or electrophilic substitution chemistry. In our own quality control, every lot faces scrutiny with NMR, LC, and titration to confirm both identity and chloride content—feedback from users tells us that side reactions in the lab drop noticeably when lot purity is high and water content sits below trace levels. That comes from drying cycles, not shortcuts. Consistent melting points and color are not incidental—they reflect a manufacturing mindset built for reliability.
Our technical team tracks specification trends. For (4-Fluoro-Phenyl)-Methanesulfonyl Chloride, we’ve tightened key parameters over time. Typical lots show purity above 99%, with chloride assays matching within a narrow window. Lower residual starting material means less need for rework. Impurities in aromatic sulfonyl chlorides can catalyze unwanted pathways in peptide, urea, or linker synthesis. Early on, some users flagged issues with moisture sensitivity. By rethinking our drying protocol and packaging, we now deploy product with lower water content, sealed under dry nitrogen in glass or PTFE-lined containers. That extra handling step has paid dividends in extended shelf life and easier handling downstream.
Custom synthesis is part of our DNA. Several years back, a leading pharmaceutical customer faced trouble scaling a methylsulfonylation route to a key fragment. Yield loss traced back to variability in sulfonyl chloride source. Talking through the problem, we benchmarked our batches against competitors and adjusted our process. That partnership taught us that off-spec supply slows entire programs, and those delays ripple up the value chain. On the research side, we’ve supported teams pursuing fluorinated bioisosteres, radiolabeling routes, and next-generation herbicides. Each of those fields uses our sulfonyl chloride for the same reason: reliable arylation, reproducibility, and strong activation without fuss.
Plenty of suppliers list similar compounds. Some aim for the lowest possible price, others play the sourcing game with intermediates made offshore. Our philosophy centers on full in-house production—from raw material purchasing to final purification. That control gives us tighter reins over solvents, temperature holds, and contaminant thresholds. Over the last decade, technical audits by multinational customers have guided incremental upgrades in reactor hygiene, reagents, and environmental controls. Feedback from experienced chemists spurred us to move away from metal canisters in favor of non-reactive packaging—a lesson learned after shelf samples showed trace leaching.
We still see reactions gone awry due to mishandled, degraded sulfonyl chlorides, especially those that absorb moisture in transit. Our team trained logistics staff to notice these pitfalls, and our warehouse does not treat sulfonylation agents like shelf-stable commodity stocks. Orders go out with just-in-time manufacture dates, humidity indicators, and package tracking, so end-users can plan syntheses with confidence that their reagent has not passed its prime. Projects on tight deadlines value that transparency and regular communication on delivery status and lot analysis. For sensitive projects, we offer lot reservation and custom split-packaging, reducing the risk of repeated container breaching on large-volume orders.
Sulfonyl chlorides can sting, corrode, and self-react, so responsible makers never lose sight of chemical safety. Over the years, we built a rigorous in-facility tracking protocol that logs each reaction, wash, and filtration. Regular plant audits by certifying bodies scrutinize our containment and emergency response measures. We don’t take shortcuts with volatile intermediates or waste management—our record stands on years of clean EPA audits and zero lost time incidents involving chlorinated intermediates. Our own lab teams run real-world application trials of every new lot, vetting reactivity and compatibility with downstream transformations. This hands-on approach allows us to spot trends before customers do and adjust upstream processing as needed.
Market prices for specialty reagents can swing widely depending on batch size, purification throughput, and raw material volatility. By securing advance contracts with upstream fluorination partners, we buffer customers from sudden cost spikes. More production shifts to continuous-flow reactors trimmed both waste and per-kg labor, helping us keep quality high without pricing out smaller labs or research groups. We prioritize keeping lead times reasonable—disruptions cost real money and slow discovery. Our mix of smaller pilot-scale runs and bulk production lets us meet both exploratory and scale-up needs with minimal backorder risk.
Some buyers cut corners with alternate grades or less refined sulfonylation agents, sometimes sourced through complex supply chains that obscure origins and controls. Our technical feedback includes residue analysis and side-by-side reaction trials run by internal and external labs. Consistency pays off in lower impurity profiles, higher yield, and fewer headaches during regulatory audits. We know chemists want more than a label—they need a reagent that behaves predictably, dissolves readily, and stays chemically sharp to the last gram in the bottle. Our specifications don’t rest at meeting minimums—they reflect accumulated know-how and a constant drive to tweak, test, and improve.
Nearly every month, an R&D scientist comes with a new coupling concept, linker, or fragment requiring custom downstream chemistry. We collaborate closely, offering different batch sizes, solvent preconditioning, or alternate packaging on request. Some routes work better with a fresh lot, while others have found success storing product over several months. We track these patterns and share best handling practices in technical bulletins rooted in experimental data, not marketing lingo. Real-world feedback flows between plant, warehouse, and application chemists. That cross-talk builds trust and flags improvement opportunities in process, quality, and documentation.
Chemical production brings responsibility, especially with halogenated reagents. Our plant uses closed-cycle solvent recovery, on-site scrubbers, and rigorous waste tracking to ensure every batch minimizes byproduct and emissions. Years ago, drain testing revealed trace organofluorine leachate. We responded with new resin filtration and doubled per-batch waste testing, and the problem vanished. We return drums for recycling and offer support for proper empty-container disposal down the supply chain. Responsible stewardship shapes every improvement—not just for compliance, but because generations rely on today’s choices.
Each new drug scaffold, protected linker, or polymer crosslink demands tools that deliver at the bench. This molecule rarely gets fanfare, but it has backed new-process patents, streamlined amide bond formation, and simplified difficult fragment introductions. Reliable sulfonyl chlorides like ours don’t just facilitate synthesis—they close the gap between bench research and scalable manufacturing. Teams trust our product not just because of purity, but because every piece of our process stands up to scrutiny and real-world use.
We keep learning alongside our customers. The first time a new impurity cropped up in a downstream reaction, we didn’t reach for off-the-shelf solutions—instead, we set up internal parallel syntheses, mapped root causes, and took steps to adjust purification. That spirit of joint improvement, not rote specification, shapes everything from our batch records to finished product. Customers get honest feedback, real technical guidance, and an open line of communication. We take pride in knowing that the chemistry behind every molecule is deeply understood, professionally monitored, and delivered with the hands-on service that comes from making—not brokering—chemicals.
Our journey with (4-Fluoro-Phenyl)-Methanesulfonyl Chloride brings decades of trial, correction, invention, and partnership. Each lot sent out carries with it the assurance that our team has examined the details, not just the numbers on a certificate. It’s not a commodity for us, nor an anonymous line item—it’s a daily task, a responsibility to researchers solving real problems. Those working at the frontiers of discovery know they can depend on what arrives from our plant. That’s the difference you experience when you work directly with a chemical manufacturer who stands behind the product, not just as a supplier, but as a partner in innovation.