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HS Code |
428163 |
| Chemical Name | 2-Methyl-5-Nitrobenzenesulfonyl Chloride |
| Cas Number | 13130-21-5 |
| Molecular Formula | C7H6ClNO4S |
| Molecular Weight | 235.64 g/mol |
| Appearance | Yellow crystalline powder |
| Melting Point | 83-86 °C |
| Boiling Point | Decomposes |
| Solubility | Slightly soluble in water, soluble in organic solvents |
| Density | 1.6 g/cm³ (approximate) |
| Purity | Typically ≥98% |
| Storage Conditions | Store in a cool, dry place and keep container tightly closed |
| Hazard Class | Corrosive, Irritant |
| Smiles | Cc1ccc(cc1[N+](=O)[O-])S(=O)(=O)Cl |
| Inchi | InChI=1S/C7H6ClNO4S/c1-5-2-3-6(9(11)12)4-7(5)14(8,10)13/h2-4H,1H3 |
As an accredited 2-Methyl-5-Nitrobenzenesulfonyl Chloride factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The packaging contains 25 grams of 2-Methyl-5-Nitrobenzenesulfonyl Chloride in a tightly sealed amber glass bottle, labeled with hazard warnings. |
| Shipping | 2-Methyl-5-Nitrobenzenesulfonyl Chloride is shipped as a hazardous material. It should be packed in tightly sealed, chemical-resistant containers, clearly labeled, and transported in accordance with local, national, and international regulations. Protect from moisture and physical damage, and ensure proper documentation for safe handling and emergency response during transit. |
| Storage | 2-Methyl-5-Nitrobenzenesulfonyl chloride should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from moisture. Keep it away from heat, direct sunlight, and incompatible substances such as bases, strong oxidizers, and water. Handle and store under inert atmosphere if possible, and always use appropriate protective equipment to avoid exposure. |
Applications of 2-Methyl-5-Nitrobenzenesulfonyl Chloride in Industrial Manufacturing2-Methyl-5-Nitrobenzenesulfonyl Chloride serves as a critical intermediate in a range of industrial sectors, primarily valued for its sulfonylation and functional group transformation capabilities. Our expertise as an original manufacturer supports established downstream integration in specialized synthesis, adhering closely to international standards and quality controls across diverse application fields. 1. Pharmaceutical Intermediate SynthesisMany commercial Active Pharmaceutical Ingredients (APIs) require advanced aromatic sulfonyl chloride intermediates for controlled sulfonylation steps. This compound allows fine-tuning of reactivity for targeted functional group modifications, particularly in stepwise multi-stage API production, such as cephalosporin antibiotics or certain anticancer agents. During these synthesis routes, operators introduce the compound at specific nitration or sulfonation stages, optimizing yields and minimizing by-products under validated conditions, and subject all handling to stringent pharmaceutical GMP and ICH guidelines. Industry compliance standards
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2. Agrochemical Intermediate ManufacturingProducers of modern crop protection products depend on reliable sulfonyl chloride intermediates to synthesize selective sulfonylurea and triazine herbicide actives. Large-scale operations require the material’s high purity and consistent specification to ensure downstream conversion to sulfonamide and carbamate linkers. Production mainly introduces the raw material in the early-to-mid stage as a functionalization partner, allowing for high selectivity in industrial reactors and conformity with agrochemical quality management frameworks and pre-registration testing requirements. Industry compliance standards
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3. Dye and Pigment Intermediate ProductionThe fine chemicals segment for organic colorants uses aromatic sulfonyl chlorides to achieve high-affinity sulfonation and stabilization of pigment structures. Manufacturing dye precursors—such as azo or anthraquinone dyes—requires predictable reactivity to introduce sulfonic acid groups, often under high-throughput, reproducible batch conditions. This material enters at the aromatic modification phase, under tightly specified process controls to support regulatory-compliant end products for the textile, plastic, and ink sectors, all of which must meet specific environmental and consumer safety parameters. Industry compliance standards
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4. Specialty Polymer ModificationAdvanced specialty polymer producers utilize aromatic sulfonyl chlorides as cross-linking or end-capping reagents to impart functional groups for ionic exchange membranes, medical devices, and electronic encapsulants. The intermediate’s reactivity spectrum allows process engineers to graft sulfonic acid or sulfonamide moieties onto polymer backbones—enhancing hydrophilicity, thermal stability, or conductivity in high-value finished forms. Typical use involves metered feeding into polymer melt, solution, or emulsion processes—performed under monitored conditions mandated by sector-specific QMS and environmental legislation. Industry compliance standards
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From the first kilo we produced in our facility, 2-Methyl-5-Nitrobenzenesulfonyl Chloride has been more than an entry in a catalog for us. It’s a specialty intermediate that underpins a range of demanding reactions, especially where strong reactivity and selectivity are non-negotiable. Over years of manufacturing, the compound’s role has moved from niche to integral in fields including pharmaceuticals, agrochemicals, dyes, and advanced material sciences. Handling its production in-house not only isolates the process from supply chain interruption but lets us pay close attention to both purity and safety, two ideas that rarely get enough consideration outside the chemical plant floor.
Every batch of 2-Methyl-5-Nitrobenzenesulfonyl Chloride coming off our lines reflects decisions made through experience rather than routine. As a crystalline solid with a molecular formula of C7H6ClNO4S, and a molecular weight logged at 235.65 g/mol, this sulfonyl chloride derivative demands a purity routinely maintained above 98%. Today’s innovation cycles push downstream partners to test the limits of their chemistry, and they tell us where impurities compromise results. Instead of targeting just a “specification sheet” number, we focus on delivering a material with low moisture content, consistent particle size distribution, and tight control over trace chlorinated byproducts and inorganic residue.
Reactivity depends not just on the active functional group but on everything else packed into each sample bag or drum. If moisture creeps in, hydrolysis under ambient storage can create downstream headaches. To counter this, we seal product under dry nitrogen and have invested in upgraded packaging that resists diffusion and mechanical puncture. Nitrogen handling, sealed filling, and real-time in-process quality checks are routine for us — these are the things that separate finished product headed for critical synthesis from material destined for less sensitive environments.
Looking at the manufacturing side, the real challenge with sulfonyl chlorides comes from their reactivity. Their tendency to hydrolyze or engage in side reactions means the batch must move quickly but under precise conditions. We select solvents that favor minimal byproduct generation and batch sizes that allow us to stabilize thermal profiles, avoiding excessive local heating or cooling. Our reactors are jacketed, automated for careful addition, and designed for inert gas blanketing. These steps are more than technical checkboxes; each one grew from process data, safety incidents, and downstream partner feedback.
The hydrochloric acid evolution in the chlorination process poses an engineering problem — it isn’t just about capturing the gas but about keeping operator exposure close to zero. Dedicated scrubber units, sensors, and remote controls form the backbone of our setup. We use process analytical technology to monitor chlorination progress in real time, dialing in on the endpoint with enough accuracy to avoid over-chlorination or incomplete conversion. These are real ways a manufacturer shapes the actual properties of the sulfonyl chloride: impurity spectra, color, and—critically—repeatability from lot to lot.
2-Methyl-5-Nitrobenzenesulfonyl Chloride is chosen because it carries both an activating sulfonyl chloride group and an electron-withdrawing nitro group, pairing electrophilicity and resonance effects. This unique substitution pattern allows for precise functional group introduction in organic frameworks. For instance, in pharmaceutical research, chemists use this compound for sulfonamide formation, where selectivity and mild conditions matter. Unlike benzenesulfonyl chloride, which can overreact or lead to excessive byproduct formation, this methyl-nitro derivative tempers reactivity, granting higher yields and fewer side products—a fact supported by several peer-reviewed studies.
Agrochemicals often demand functional intermediates capable of tuning bioactivity. In our work with crop science firms, they favor our product due to the balance between reactivity and the presence of a modifiable methyl group. Dyes and pigment makers leverage the nitro group for added color stability during application and weathering. High-purity product does not just boost final yield but prevents discoloration and polymerization—outcomes that would otherwise surface during application testing.
Process chemists keep telling us impurity profiles matter even more than headline purity. Residual sulfur dioxide, byproduct methylated aromatics, or unreacted chlorinating agents in sulfonyl chlorides cause off-odors, corrosion, and even toxic off-gassing during scale-up. Direct feedback from our user base shapes each plant modification and raw material audit.
Working in the plant, colleagues often debate the nuances between different benzenesulfonyl chloride derivatives. Some ask: why not just stick with p-toluenesulfonyl chloride or the unsubstituted benzenesulfonyl chloride? The answer, visible in every kilo we ship, sits in the substitution pattern. Adding the methyl at the 2-position, with a nitro at the 5-position, tunes the electron density across the aromatic ring. This influences everything from reactivity during amine sulfonylation to the downstream pharmacokinetic properties of the final molecule.
Compared to p-toluenesulfonyl chloride, the nitro group on the meta-position in our compound lowers electron density at the ring, dampening untoward side reactions that complicate purification and scale-up. The presence of the methyl group can increase lipophilicity—relevant for some synthetic targets—while p-toluenesulfonyl chloride does not offer this same balance. These structure–activity lessons drive further process optimization and quality checkpoints within our facility.
Handling differences extend to the plant floor too. p-Toluenesulfonyl chloride tends to be more forgiving in handling and less moisture-sensitive, but it cannot give the precise reactivity required for more sensitive pharmaceutical syntheses. For applications where reactivity and selectivity need tight control, especially in late-stage functionalizations, our product’s unique structure pays dividends. This is more than academic; a failed batch due to unwanted side reactions costs time and money and may waste weeks of synthetic work—a risk that process engineers working shoulder-to-shoulder with us remind us every month.
As manufacturers, our challenge comes not from scale alone but from the complexity of controlling quality across dozens of finished lots shipped each year. Batch reactors, feedstock purity variation, and the need to satisfy both small-batch researchers and large-scale formulators require agility. There’s a tendency to see sulfonyl chlorides as commoditized, but users in regulated industries know the difference the right impurity fingerprint makes. Inconsistent quality adds troubleshooting time, repeat runs, and safety audits—none of which customers appreciate.
Our own scale-up history with 2-Methyl-5-Nitrobenzenesulfonyl Chloride has forced process upgrades in plenty of ways. Early batches struggled with localized overheating and trace sulfonic acid residues, both traced to poor cooling and incomplete phase separation. That led to investments in stirred reactor systems with better temperature mapping and a more robust drying protocol, cutting residual water content down to less than 0.1%. Sourcing anhydrous reagents consistently has proven just as important as reactor hardware—lessons written into the standard operating procedures followed on every shift.
Operators on the line have devised a dual-funnel addition approach, metering in chlorinating agents at a pace that stabilizes exotherms and reduces the chance of runaway. Sensors and on-site analytical capacity give us a window into each transformation step. These steps build confidence not only in the product’s final quality but in its reproducibility from batch to batch—something researchers and purchasing directors have reliably fed back to us as a deciding factor in repeat orders.
Sulfonyl chlorides present their own safety landscape. Our years of experience underline the need for dry, cool, well-ventilated storage, and for always keeping moisture away, since accidental hydrolysis not only deactivates the compound but generates heat and HCl fumes. Our packaging is bi-layered and sealed under nitrogen; we train logistics handlers to keep handling windows tight and monitor every shipment for seal integrity. These procedures do not end with us—they enable end-users to avoid unnecessary exposure risk, waste, and lost material.
Regulatory compliance in our sector involves not only documentation, but testing verification. As REACH and other frameworks tightened, our in-house compliance team realigned documentation practices and batch traceability. Every lot can be traced to its reactor run, operator shift, and raw material order. That intimacy with our own operation is backed by decades of records, often reviewed and audited by third-party and customer teams alike. Over time, these standards cut down on late-stage regulatory questions for users and enhance the safety baseline of both our process and the final product in their workflows.
Supplying 2-Methyl-5-Nitrobenzenesulfonyl Chloride is more than a sales function for us. Downstream chemists at both research and commercial scale need information about stability, reactivity, and impurity profile that goes beyond a generic certificate of analysis. Direct dialogue with customer R&D and technical teams reveals emerging reaction conditions, incompatibilities with certain solvents, and requests for custom packaging. In supporting dozens of customer method validations, we've shared data sets, stability curves, and experience reports from plant trials — exchanges that foster trust rather than transactional one-offs.
Through this process, we’ve learned that end-user feedback is direct input for future batch improvements. We track every inquiry, nonconformance report, and special requirement, bringing them up at quarterly process review meetings. For example, one biotech customer reported minor discoloration in material stored for six months under ambient light—a signal for further packaging improvements and dark storage recommendations, which then led to new drying and light-barrier steps in our process. Experience teaches that persistent interaction with field chemists creates a loop where both product and process constantly evolve.
Chemical manufacturing always comes with environmental responsibilities. For 2-Methyl-5-Nitrobenzenesulfonyl Chloride, careful waste stream segregation—especially hydrochloric acid, spent solvents, and off-spec intermediates—means lower downstream environmental risk. Our facility captures, neutralizes, and monitors all vent gas and liquid effluent streams, reporting discharge data as part of both local compliance and broader sustainability initiatives. The closed-loop solvent recovery system installed after a process audit now recycles over 75% of chlorination solvents, reducing both cost and overall emissions from manufacturing.
In addition to regulatory requirements, we see waste reduction as a competitive advantage. Smaller secondary waste streams give us cleaner products and happier neighbors in the industrial park. Customer feedback has spurred us to examine lifecycle impacts, leading to support of downstream product take-back and recycling systems, and transparency around carbon and water usage tied directly to batch output.
Markets and regulations are always in motion. Researchers move rapidly into new application territory, including more exotic biologically active compounds, novel dyes, and performance materials demanding fine-tuned reagents where trace impurities change product function completely. Continuous investment in plant upgrades, analytical instrumentation, and operator training keeps our process flexible. In-house expertise doesn’t just cut downtime or scrap rates—it gives us the agility to run custom lots, deliver special packaging formats, and guarantee consistent profiles for critical downstream reactions.
Benchmarking performance against global competitors and collaborating with research clients pushes us to refine the process further. We run comparative studies, reviewing impurity profiles and reaction performance under varying conditions. Our technical team regularly attends symposia, sharing best practices and collecting insights across industries. These direct lines of communication cement our role as a specialist producer rather than a generic supplier. In turn, customers trust that our 2-Methyl-5-Nitrobenzenesulfonyl Chloride will perform as expected—batch after batch.
Producing 2-Methyl-5-Nitrobenzenesulfonyl Chloride is a daily exercise in chemistry, engineering, and cooperation. The path from raw materials to a reliable specialty intermediate is shaped by accidents, analytical challenges, regulatory shifts, and, above all, customer trust. The real measure of a manufacturer is neither the certificate of analysis nor the marketing pitch, but the depth of experience, openness to improvement, and respect for the downstream partner’s own expertise. We take pride in seeing this compound move out of our plant and into thousands of real-world transformations, proving itself—one batch at a time.