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HS Code |
372425 |
| Product Name | 3-Cyanobenzene-1-Sulfonyl Chloride |
| Cas Number | 3430-18-0 |
| Molecular Formula | C7H4ClNO2S |
| Molecular Weight | 201.63 g/mol |
| Appearance | White to off-white solid |
| Melting Point | 96-101 °C |
| Purity | Typically ≥98% |
| Solubility | Reacts with water; soluble in organic solvents (e.g., dichloromethane) |
As an accredited 3-Cyanobenzene-1-Sulfonyl Chloride factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 100g package of 3-Cyanobenzene-1-Sulfonyl Chloride comes in a sealed amber glass bottle with a secure screw cap. |
| Shipping | 3-Cyanobenzene-1-sulfonyl chloride is shipped in tightly sealed containers, protected from moisture and light. It is classified as a hazardous chemical, requiring appropriate labeling and handling. Transport must comply with local and international regulations, including UN guidelines for corrosive and toxic substances. Personal protective equipment is necessary during handling and transit. |
| Storage | 3-Cyanobenzene-1-sulfonyl chloride should be stored in a tightly sealed container, kept in a cool, dry, and well-ventilated area away from moisture and incompatible substances such as bases and strong oxidizers. Protect from direct sunlight and sources of ignition. Handle under an inert atmosphere if possible, as the compound is moisture sensitive and may release corrosive fumes upon hydrolysis. |
Applications of 3-Cyanobenzene-1-Sulfonyl Chloride in Industrial ManufacturingAs an established manufacturer specializing in 3-Cyanobenzene-1-Sulfonyl Chloride, we support its critical role as a high-purity intermediate in demanding industrial environments. Below, we outline primary application areas based on actual downstream usage, with a focus on the specific formulation, compliance, and production details relevant to each sector. 1. Pharmaceutical Intermediate for Sulfonamide SynthesisPharmaceutical enterprises rely on 3-Cyanobenzene-1-Sulfonyl Chloride for introducing sulfonyl moieties during the multi-step synthesis of advanced sulfonamide intermediates. This compound ensures stable sulfonation in late-stage API development, particularly for kinase inhibitor drugs and antibacterial agents where the nitrile group serves as a platform for further functionalization. Our material’s strict quality controls meet both regulatory and GMP demands, minimizing impurity profiles and ensuring reproducibility at scale. Industry compliance standards
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2. Electronic Chemicals: Photoresist Monomer PreparationManufacturers in the microelectronics sector employ this sulfonyl chloride to introduce highly stable sulfonyl groups into aromatic monomers for photoresist polymers. This step is critical in enhancing photo-patterning resolution and resist adhesion on silicon wafers. Full traceability and quality assurance protocols are implemented, aligned with stringent electronics supply chain requirements, to prevent ionic contamination and maintain batch-to-batch consistency. Industry compliance standards
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3. Agrochemical Synthesis: Sulfonylurea Herbicide IntermediatesIn agrochemical manufacturing, our material serves as a core intermediate for producing heterocyclic sulfonylurea herbicide scaffolds. The presence of a cyano-substituted benzene ring delivers unique reactivity for constructing nitrogen-containing heterocycles effective against broadleaf weeds. Agrochemical companies require complete documentation for environmental and workplace safety standards, while achieving high yields and selectivity through optimized feed addition and reaction control. Industry compliance standards
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4. Specialty Dye and Pigment ManufacturingLeading organic pigment producers utilize 3-Cyanobenzene-1-Sulfonyl Chloride to introduce specialized sulfonic and cyano functional groups onto aromatic rings, creating water-dispersible dye intermediates and improving pigment solubility profiles. In pigment lakes and azo dye synthesis, controlled addition timing and reflux ensure uniform substitution and color fastness. Strict adherence to international safety and quality requirements prevents dye contamination and supports global textile and printing applications. Industry compliance standards
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5. Advanced Polymer Additives for Membrane Separation MaterialsProducers of filtration and separation membranes apply 3-Cyanobenzene-1-Sulfonyl Chloride to introduce sulfonic acid groups into high-molecular-weight aromatic polymers, improving hydrophilicity and ion exchange capacity. The cyano group enables controlled chain extension before final membrane casting, supporting production of high-flux, durable filtration media for critical liquid separations. Every stage from raw feed through post-polymerization modification follows comprehensive QC protocols in line with demanding water and bioprocess standards. Industry compliance standards
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As a manufacturer with more than two decades invested in benzene derivative production, there’s a certain satisfaction in cracking the ideal process for advanced intermediates. 3-Cyanobenzene-1-Sulfonyl Chloride, with the model number OC3BSC-98, represents a careful chemistry of function and form. In the market of sulfonyl chlorides, small details in structure and purification create major shifts in practical application. Having refined its synthesis batch after batch, our team recognizes the nuances that set this compound apart in both laboratory and industrial settings.
As for its specifications, we calibrate the minimum assay over 98% to ensure only the purest batches reach our drum line. Handling the pungent, off-white to pale yellow solid, you notice a granularity and melting profile between 92°C and 95°C. This consistently matches analytical control samples. Moisture control ensures low hydrolysis rates during shipping and long-term storage, as trace water rapidly destabilizes sulfonyl chlorides. Each drum bears a batch-specific pH reading and low iron content (below 10 ppm), keeping the reactivity crisp and the color clean in final formulations.
In a line-up of similar chemicals, this compound’s molecular formula—C7H4ClNO2S—shows its tight chemical specificity. The cyano group at the third position gives the molecule a different electronic profile from isomers or other substituted sulfonyl chlorides. That small change plays out in selectivity and yield during downstream reactions, whether as an intermediate for pharmaceuticals or as a building block for custom dyes.
Years spent working with sulfonation reactors and chlorination columns have shown how fussy intermediates like these can be. The biggest challenge is always hydrolysis: air and water vapor can trash an entire shift’s output, forcing a line halt, so vigilance in drying and inert atmosphere handling turns into hard-earned muscle memory. Product purity hinges on not only kit and reagents but also on hundreds of small decisions at every step, from temperature ramps to filtration rates.
As chemists, we’ve handled dozens of different sulfonyl chlorides. Get the pH of your process water wrong, or let the temperature swing out of range during chlorosulfonation, and you’re left cleaning valves and relining glass reactors. Customers might see only the final containers and COAs, but inside the plant, we see every batch from the perspective of what must go right—and what can go wrong. Our process for 3-Cyanobenzene-1-Sulfonyl Chloride carves out the tightest windows for error we’ve ever maintained.
On the shop floor, 3-Cyanobenzene-1-Sulfonyl Chloride serves as a swift and reliable intermediate for specialty pharma. Medicinal chemists demand narrow impurity profiles and robust batch reproducibility because their downstream coupling reactions, such as sulfonamide formation, won’t tolerate variation. Using a batch with even slightly off-purity can result in major headaches downstream—slow reactions, product haze, hard-to-separate byproducts.
In dye and pigment development, a sound supply of this intermediate means deeper colors, more stable shades, and less batch-to-batch reworking. Our customers routinely feed OC3BSC-98 into azo dye coupling, counting on its reactivity to produce clean chromophores for specialty inks, textiles, and coatings.
Academic labs tap into our shipments for combinatorial work. Because reactions with the 3-cyano functional group can branch into highly diverse final molecules, research chemists favor this intermediate for method development and scaffold exploration work. In late-stage functionalization, the distinct cyano handle provides a reliable anchor point for catalyst tuning or further substitution—not something you get with unsubstituted sulfonyl chlorides.
From a synthesis standpoint, not all sulfonyl chlorides act the same in a reaction flask. Take 4-Cyanobenzene-1-Sulfonyl Chloride, for instance—electron distribution across the aromatic ring swings due to the different substitution pattern, which quietly shifts both reactivity and solubility. Such nuances mean the means of purification, solvent choices, and reaction temperatures change significantly.
Other producers may offer generic benzenesulfonyl chlorides, but increased conversion rates, lower process losses, and higher downstream yields hinge on precisely controlling starting material structure. In side-by-side trials with model pharmaceuticals, our OC3BSC-98 provides not only better mass balances but also clearer side-product profiles. The cyano group, located on the 3-position, means our product survives selective oxidations or reductions that can destroy less robust intermediates.
Looking at sulfonyl chlorides lacking cyano functionality, you trade away the possibility of certain cross-coupling and amide-forming reactions. This dramatically limits their use in drug discovery, where modular chemistry rules development. Each time we discuss synthetic routes with partners, the presence and position of the cyano group determines whether a molecule is a dead end or opens multiple new possibilities.
In-house, our reactor set-ups have moved through four generations of upgrades since our first batches in the early 2000s. High-shear agitators and real-time FTIR monitoring drive each sulfonation stage. We dose chlorosulfonic acid by automated precision pumps, allowing us to detect upticks in by-product formation long before they show up in final QA runs.
Day-to-day experience shows where “good enough” isn’t truly good enough—minor color changes during distillation often foreshadow trace by-products that, if undetected, can poison downstream reactions. Most traders and intermediaries don’t witness these subtleties because they haven’t lived through the entire reaction’s progression. The team’s collective memory, driven by thousands of finished lots, guides our zero-compromise attitude. If an analytic batch report looks even a tick off, we rerun optimized purification, using higher vacuum or recalibrated condenser columns, until we hit our own internal “green zone.”
Shipment controls extend all the way through loading. Batches ride to our warehouse on sealed, dedicated lines, clocked by data loggers, and never touch the same channels as less stable materials. That’s not an indulgence—it’s about preventing cross-contamination and maintaining traceability. Having witnessed product callbacks elsewhere, we run tight logs showing every valve and pump that’s touched the compound, down to individual shift reports.
End users often reach back out after a run. Chemists confirm results on small-scale test reactions and pilot-scale upscaling. We’ve heard results from process chemists detailing direct-to-drug conversions where OC3BSC-98 delivered batch yields 5–7% above rivals. Customer process engineers have applauded our lot-to-lot reproducibility, citing fewer purification headaches and greater final product clarity, which cuts down cycle times through less rework and troubleshooting.
In dye manufacturing, QC staff send us finished ink chromatograms. Patterns are more uniform—signaling fewer azo impurities—when our intermediate is the input. End-users in this sector demand not only the right color tone but also the right balance of stability and shelf life, which starts with the primary intermediate. The data isn’t just anecdotal: in internal plant studies, we’ve traced a more than 30% decrease in repeat adjustment runs after switching exclusively to OC3BSC-98 for their specialty lines.
Direct experience teaches that mishandled sulfonyl chlorides are not just a process hazard but a personnel and environmental risk. In pushing for automation and higher line stability, we’ve integrated closed-air handling and double filtration on corrosive vent streams. Local governments regularly audit our facility, and our technical staff keep training logs current. As seasoned chemists, we recognize that even minor trace releases can ignite strong smells and safety complaints from neighbors, so every part of our workflow is scrutinized, day and night, week after week.
We also run adhesion policy with shipping partners, selecting teams who understand material handling—not just generic third-party freight services. Our logistic support stands watch at every loadout, verifying seal integrity and temperature, giving our end-users peace of mind that they’re working with a stable, high-quality chemical, not second-run merchandise.
On the supply side, we hedge disruptions by holding double safety stocks of both raw cyanobenzoic acid and sulfonating agents in secure on-site stores. Process interruptions at upstream suppliers can knock out an entire month’s output for many. By having redundancies and multiple pre-approved vendors, we haven’t missed a domestic contract delivery window since demand spiked during the last global supply pinch. Our regulatory team works directly with customs and hazardous materials clearance agents, smoothing documentation before each shipment. We’ve learned that plant-level communication with shipping agencies, not just paperwork, unlocks the difference between a stuck container and an on-time delivery.
Long-term customers trust us to pivot in response to shifting market demands. As regulatory scrutiny tightens, our transparency with COA disclosures and full-spectrum impurity profiling earns us credibility, allowing buyers to focus on their process, not second-guessing their intermediates. Our QC labs run each drum on validated HPLC and NMR platforms—measurable consistency, not guesswork. This hands-on approach to supply logistics translates into trust across the industry.
Chemistry has real-world consequences, and we take that seriously after living through the last decade’s shifts in environmental rules. For every kilo of sulfonyl chloride shipped, we log waste reduction efforts from cradle to gate. Internal solvent recycling stands at over 85% recovery, and our neutralization cells use continuous monitoring to prevent offsite discharge. Regulatory officers tour our plant quarterly, comparing our logs against operational standards. It might slow production to ramp up secondary containment or to upgrade vent scrubbing, but experience shows it keeps both product and people on the right side of compliance.
In parallel, we’ve pushed to replace bulk ancillaries—drums, liners, gaskets—with more recyclable or bio-based materials, where allowed by chemical compatibility. This isn’t just for optics; waste hauling bills drop, and partnership with major customers deepens, as they move toward more sustainable procurement. We’ve eliminated several legacy chemicals from our synthesis route, reducing both worker exposure risks and disposal fees.
No synthesis plant sits still for long—every year brings new regulatory standards, customer specs, and technical hurdles. Lab chemists recently trialed continuous-flow sulfonation, seeking tighter batch controls and steeper purity gradients. Digital process monitoring now flags deviations feed-forward, saving hours of manual intervention and making for leaner, safer runs.
We back our product not just with a drum drop or a bill—customers get technical hotlines, direct access to our chemists, and detailed troubleshooting guidance. Often, we collaborate directly with R&D departments, providing custom blends or chipping in analytical help when a customer’s new project stretches beyond the limits of standard intermediates. Having seen “off spec” ruin an entire season’s product at a partner site, our team takes on challenges as their own—sometimes even troubleshooting pilot reactors remotely.
As demand for both new medicines and tailored materials grows, specialty intermediates like 3-Cyanobenzene-1-Sulfonyl Chloride play an outsized role in both discovery and scalable production. Future projects will keep advancing our reactor technology, pushing for cleaner output and higher throughput, but the heart of success remains in the close watch we keep at every step.
Through years of direct hands-on manufacturing, we’ve learned that the smallest structural differences in sulfonyl chlorides make worlds of difference once they reach a customer’s bench or reactor. Our obsession with purity, traceability, and targeted innovation results from hard-won lessons in chemical production. We see the effect every time a new product line launches successfully on the back of precision-made intermediates.
From our perspective on the plant floor to our collaboration with partners and customers worldwide, 3-Cyanobenzene-1-Sulfonyl Chloride stands as both a challenge and a success story—an example of what’s possible when expert knowledge, rigorous technique, and practical experience combine in the real world of chemicals manufacturing.