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HS Code |
404123 |
| Cas Number | 4215-94-1 |
| Chemical Name | 2-Cyanobenzenesulphonyl Chloride |
| Molecular Formula | C7H4ClNO2S |
| Molecular Weight | 201.63 g/mol |
| Appearance | White to off-white crystalline powder |
| Melting Point | 70-74°C |
| Solubility | Reacts with water, soluble in organic solvents like chloroform and dichloromethane |
| Density | 1.47 g/cm³ (approximate) |
| Purity | Typically ≥98% |
| Synonyms | 2-Cyanobenzenesulfonyl chloride; o-Cyanobenzenesulfonyl chloride |
| Storage Conditions | Store in a cool, dry place; keep container tightly closed; protect from moisture |
| Hazard Statements | Causes skin burns and eye damage; harmful if swallowed or inhaled |
| Ec Number | 224-122-0 |
As an accredited 2-Cyanobenzenesulphonyl Chloride factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 500g of 2-Cyanobenzenesulphonyl Chloride is supplied in a sealed amber glass bottle with a tamper-evident screw cap. |
| Shipping | 2-Cyanobenzenesulphonyl Chloride is shipped in tightly sealed containers, protected from moisture and light. It should be handled as a hazardous chemical, with appropriate labeling for corrosive and toxic substances. Transportation must comply with local regulations for dangerous goods, ensuring secure packaging and temperature control to prevent degradation or accidental release. |
| Storage | 2-Cyanobenzenesulphonyl chloride should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from sources of moisture and incompatible materials such as strong bases, oxidizers, and water. Protect the container from physical damage and direct sunlight. Use secondary containment to avoid accidental release, and ensure proper labeling and access by only trained personnel. |
Applications of 2-Cyanobenzenesulphonyl Chloride in Industrial ManufacturingAs a specialist manufacturer of 2-Cyanobenzenesulphonyl Chloride, we supply this key intermediate to select industrial sectors that demand precision and compliance in advanced synthesis. This application guide covers well-established downstream production segments, with details on compositional integration, operational protocols, regulatory compliance, and end product profiles specific to each field. 1. Pharmaceutical Intermediate SynthesisPharmaceutical companies employ 2-Cyanobenzenesulphonyl Chloride as a critical coupling agent and protecting group in the stepwise synthesis of numerous active pharmaceutical ingredients (APIs), particularly in the preparation of sulfonamide derivatives and kinase inhibitors. Process engineers introduce it in the early to middle stages of multi-step batch synthesis to achieve precise sulphonation under controlled conditions, often followed by further functionalization. Its high selectivity and reactivity enable tight process control and minimize off-target byproducts, supporting robust process validation for regulated product lines. Industry compliance standards
Typical usage ratio
Downstream process integration
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2. Agrochemical Active Ingredient ManufacturingProducers of crop protection chemicals utilize 2-Cyanobenzenesulphonyl Chloride for the development of novel sulfonylurea herbicides and fungicides, where selectivity and functional group compatibility are essential. The compound enters synthetic routes for specific sulfonamide and benzene sulfonyl derivatives, which function as bioactive agrochemical scaffolds. Integration typically occurs in a dedicated sulfonylation reactor train, allowing continuous monitoring of byproduct levels to meet agrochemical purity standards. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
3. Dye and Pigment Intermediate ManufacturingManufacturers in the specialty dye and pigment sector incorporate 2-Cyanobenzenesulphonyl Chloride in the benzene sulfonylation of chromophore moieties. Formulators leverage its electrophilic sulphonation capability in synthesizing azo and anthraquinone dye intermediates, critical for colorant performance, lightfastness, and application stability. Processing occurs under strict pH and temperature regulation to ensure high chroma yields while minimizing impurity carryover in final dispersions. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
4. Advanced Material and Polymer SynthesisSpecialty polymer manufacturers apply 2-Cyanobenzenesulphonyl Chloride to introduce sulfonyl groups into functional polymers, boosting ion-exchange capacities and enhancing performance of engineered membranes. Controlled sulphonylation during copolymer chain functionalization enables custom tailoring for ion exchange resins and selective membrane carriers. Plant-scale blending with polyarylene ether matrices ensures predictable substitution while maintaining polymer integrity and downstream compatibility. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
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For years, our team has worked hands-on with the intricacies of aromatic sulfonyl chlorides. In the lineup, 2-cyanobenzenesulphonyl chloride often stands apart, not just as a chemical structure, but as a material that answers to modern synthetic chemistry’s evolving demands. Chemists in the pharmaceutical and agricultural sectors keep looking for building blocks that boost selectivity, shorten synthesis steps, and cut down on waste. Our job is to supply those building blocks—and to do it with consistency, transparency, and technical clarity.
In manufacturing 2-cyanobenzenesulphonyl chloride, we don’t rely on guesswork. Our process draws from decades of experience both on the shop floor and in R&D, balancing production scale with the reliability that advanced chemistry requires. This product often goes by its CAS number, 6129-97-7, and its structure—a benzene ring with both a sulfonyl chloride and a cyano group—marks out its differences from more routine sulfonyl chlorides. That structure gives it a unique reactivity that formulation teams appreciate across organic synthesis, dyes, intermediates, and specialty chemicals.
We produce 2-cyanobenzenesulphonyl chloride under a continuous improvement model, always refining our process through feedback and analytical data. Each batch draws on well-established routes—usually starting with high-purity ortho-substituted raw materials. Temperature control, atmospheric handling techniques, and fine-tuned chlorination steps shape the product’s final purity. Yields often exceed 95 percent under optimized conditions, but even small temperature fluctuations can shift the impurity profile. Through hands-on lessons, we’ve learned the right point for workup and drying, so the final product ships as a pale to off-white crystalline solid, not a yellowed, decomposition-prone powder.
Many labs approach us about higher volumes or unique packaging for 2-cyanobenzenesulphonyl chloride. These questions rarely surprise us. Small-scale syntheses in glassware can’t always predict the quirks and byproducts that crop up at scale. Our experience covers both kilogram and ton levels, so we pick vessels and inert systems suited for the product. No batch leaves our site without GC, HPLC, and water testing. Moisture is a main enemy here—trace water drives hydrolysis, forming acidic byproducts and impurities. That’s why we pack the material under nitrogen and deliver solid product, not exposed solutions.
Some customers look for purity numbers and nothing else. But even a purity of 99.5% doesn’t mean much if the remaining half-percent includes problematic side products. From real-world troubleshooting, we know that color, melting range, and stability actually shape the chemical’s function. Our product typically melts between 78-82°C. Too much deviation in this range often signals incomplete reaction or high levels of isomeric material.
Anyone preparing sulfonamides or working in coupling chemistry appreciates how the cyano group’s position on the benzene ring shapes regioselectivity. The ortho (2-) substitution really changes how the sulfonyl chloride interacts with nucleophiles. Our QC doesn’t just rely on instrumental data—we go as far as running representative reactions, watching for side-product formation and yield drops.
Trace metals, water content, and color form the major flags in end-use feedback. Strict drying—not just a quick desiccator run—keeps free water below 0.1%. We screen for chloride, sulfate ions, and other halogen traces, particularly since downstream processes can be catalytic or highly sensitive to contamination. In pharma and agrochemical applications, the wrong impurity profile means repeat synthesis and lost time. We manufacture to standards that let the product hold up in multistep synthesis, scale-up trials, and commercial active ingredient production.
Over the years, we’ve watched the main uses of 2-cyanobenzenesulphonyl chloride shift. It started as a specialty item for research-scale transformation. Today, demand comes from large players in pharmaceuticals, especially for making heterocyclic scaffolds where the ortho-cyano position boosts reaction selectivity. Large batch preparation for regulatory submission needs not just high purity, but documentation of consistency—a point we address through batch certificates and full analytical traceability.
The chemical plays a defining role in protecting groups and coupling agent synthesis. In practice, we see it put to use in:
Process teams regularly reach out to discuss solvent choice, reaction setups, and troubleshooting yield or color. We commonly recommend working in anhydrous environments, using chlorinated or aromatic solvents that won’t react adversely. Experiences with nucleophilic aromatic substitution show that the ortho-cyano group can block undesired side reactions, a quality that often ends up saving costly reruns and lengthy purifications. Some of our clients have reported that switching to our product eliminated recurring issues with colored byproducts—problems that trace back to hydrolytic instability in less rigorously produced material.
Research shops and pilot plants compare 2-cyanobenzenesulphonyl chloride to related compounds—mainly simple benzenesulfonyl chlorides or analogues with the cyano group in the para or meta position. In hands-on synthesis, those differences aren’t subtle. Our ortho-cyano product throws up less off-target sulfonation, especially under basic work-up, leading to crisper yields and easier purification.
Drop-in substitutions for the para- or unsubstituted versions usually run into issues with thermal instability or side-chain reactivity. In one scaling campaign, a pharma customer shifted to our 2-cyano version and trimmed their overall synthetic route by one step. That single modification not only reduced waste but also shrank chromatography costs. From the plant side, we track these outcomes—each win feeds into how we maintain the product line, staff training, and analytical focus.
One common competitor product is para-cyanobenzenesulphonyl chloride. It tends to break down faster under basic or high-temperature conditions. Users have shown us side-by-side data; decomposition levels, when tracked by HPLC, point strongly toward better half-life with our ortho-cyano product. Feedstock availability also divides us from the field. We source ortho-substituted aromatics from audited producers, always checking supply continuity to fend off seasonal variation and quality shocks. That translates downstream into lots that react the same way week after week.
Building batches at industrial scale reveals flaws in synthesis routes that rarely show up in the lab. Several runs ago, a subtle spike in hydrolysis byproducts set off alarms. Extra investigation traced it to a minor leak in one reactor’s inert gas line. That single equipment issue triggered a cascade of product color changes, higher acid content, and off-spec crystals. Since then, we’ve overhauled our atmosphere monitoring—installing inline sensors and shifting to real-time digital tracking instead of periodic manual checks. These upgrades didn’t just raise our own confidence, but let customers receive a product that survives long storage or lengthy shipping without edge-case failures.
Waste management also weighs heavily. Chlorinated effluent and acidic waste streams can’t just disappear. Local regulations here push us toward multi-stage scrubbing and batch-neutralization. Every tonne brings new compliance documentation, but it forces us to get better at raw material use and energy conservation. Some shipment schedules depend on timing with permitted waste pickups—a detail most outside the chemical trade don’t see, but which shapes how quickly we can pivot from one customer’s needs to the next.
Every year brings a handful of product returns or out-of-spec reports. Most come from uncontrolled storage conditions or exposure to moisture, yet trends matter more than isolated errors. One series of returns prompted us to revisit our packaging methods—swapping older polyethylene liners for multilayer aluminum pouches that offer stronger barriers against air and water ingress.
Manufacturer-level traceability means we always keep archived samples from every lot. If an issue crops up months after delivery, we pull these samples and run the same analytical checks we used for release. This cycle of investigation and reporting closes the loop—product complaints turn into actual process improvements. More clients now ask about shelf-life documentation, and in response we’ve started offering real-time and accelerated stability data going back several years.
Market volatility has grown lately, with swings in both raw material price and freight. Lessons from recent disruptions have pushed us to build a larger buffer stock of starting chemicals and intermediates. Our relationship with upstream suppliers matters as much as our relationship with the end customer; if one fails, so does the finished product. To build redundancy, we work with at least two independent, audited vendors for each critical input.
Packaging materials can be nearly as scarce as chemical components. In some years, resin shortages or shipping delays slowed outgoing loads despite full inventories. Our team learned to adapt—sourcing local packing or shifting to returnable containers for domestic runs. We share monthly reports with clients in sensitive supply chains, flagging risk areas so no one gets caught by surprise.
2-cyanobenzenesulphonyl chloride requires more respect than simply weighing out in a hood. Fielding questions from new users, we find that most accidents happen during charging and post-reaction workup, not during the reaction itself. Hands-on support, not just a written guide, often prevents spoilage or exposure incidents. We run walkthroughs on glove choice, scale-up safety, and neutralization steps for both acids and chlorinated gases. These practical measures have translated into fewer lost batches and safer scale-ups.
For new clients, we often set up short training sessions or supply demo packs for in-house evaluation before committing to full-scale use. Feedback from these pilots flows back into production notes, tightening specifications or storage instructions where real-world handling has raised risks or flagged confusion.
Commercial chlorination methods, left unchecked, generate waste and greenhouse emissions. Our plant has invested in condensation-recapture and on-site neutralization technology, pulling value back from offgassed HCl and solvents. We’ve shifted several upstream reagents to locally synthesized versions, reducing both shipping miles and risk of border delays. Some noncritical steps now use greener solvent systems or energy-efficient reactors.
Beyond the plant boundary, we partner with regulated disposal firms for every lot of acid and chlorinated washings. We maintain documentation for internal audits and client traceability, reflecting the industry’s move toward transparency and shared responsibility. The myth that specialty chemicals must always come with heavy environmental cost just doesn’t match our experience.
Many competitors post the same claims: high purity, batch consistency, fair price. The reality is more complicated. Our background—actually making the stuff, day in and day out—means we know every step where impurities sneak in, every tweak that boosts stability. Our ortho-substituted material doesn’t just sit as another catalog offering. It has evolved, shaped by every kilo sold, every lab trial rerouted from rejected batches, and every scale-up that risked more than just paperwork.
We keep learning from unusual use cases—clients exploring photoreactive polymers, or those wanting extended storage for seasonal batch runs. Their challenges trigger shifts in our storage protocols, packaging methods, and staff training. In contrast to third-party blenders, our main tool isn’t the spec sheet—it’s the process memory built up from thousands of cycles, each logged and reviewed.
What truly sets our 2-cyanobenzenesulphonyl chloride apart isn’t only the presence of a cyano group in the ortho position, nor just analytical numbers. It’s the lived experience monitoring every drum and every reaction tank; troubleshooting leaks and learning the minor signs of product drift; and listening when chemists figure out new ways to use, handle, or transform what leaves our floor.
As the chemical and pharmaceutical industries head toward greater complexity, specialty building blocks like ours have a bigger role to play. Substitution patterns once treated as niche now form the backbone of more selective routes and greener chemistry. Our manufacturing approach will keep adapting—tightening controls, deepening feedback loops, and investing in both new gear and ongoing staff education.
Demand never stays flat, so neither do the hurdles. But by keeping the process close—never relegating oversight to a distant desk or distributor—we’ve kept our product robust through changing regulations, market surge, and new technical standards. For us, 2-cyanobenzenesulphonyl chloride isn’t just a commodity line; it’s an evolving project, the sum total of what manufacturing really means: discipline, attention, and a commitment to making advanced chemistry possible at the working bench and the plant floor alike.