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4-Chloro-3-Nitrobenzenesulfonyl Chloride

    • Product Name 4-Chloro-3-Nitrobenzenesulfonyl Chloride
    • Alias p-Chloro-m-nitrobenzenesulfonyl chloride
    • Einecs 221-516-2
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
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    Specifications

    HS Code

    833641

    Product Name 4-Chloro-3-Nitrobenzenesulfonyl Chloride
    Cas Number 6303-21-5
    Molecular Formula C6H3Cl2NO4S
    Molecular Weight 256.07 g/mol
    Appearance Yellow to orange crystalline powder
    Melting Point 105-109°C
    Boiling Point Decomposes
    Solubility Slightly soluble in water, soluble in organic solvents like dichloromethane
    Density 1.74 g/cm³ (approx.)
    Purity Typically ≥98%
    Synonyms 4-Chloro-3-nitrobenzenesulfonyl chloride, Chloronitrobenzenesulfonyl chloride
    Storage Conditions Store in a cool, dry place, under inert atmosphere, away from moisture
    Hs Code 29041090

    As an accredited 4-Chloro-3-Nitrobenzenesulfonyl Chloride factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 25g amber glass bottle is sealed, labeled with "4-Chloro-3-Nitrobenzenesulfonyl Chloride", hazard symbols, and storage instructions.
    Shipping **Shipping Description:** 4-Chloro-3-Nitrobenzenesulfonyl Chloride must be shipped in tightly sealed containers, protected from moisture and incompatible materials. Transport should comply with regulations for hazardous and corrosive chemicals. Use appropriate labeling and documentation. Store and ship at room temperature with secondary containment to prevent leaks and damage during transit.
    Storage 4-Chloro-3-Nitrobenzenesulfonyl Chloride should be stored in a cool, dry, well-ventilated area away from moisture and incompatible substances such as strong bases and oxidizing agents. Keep the container tightly closed, protected from light, and clearly labeled. Store under inert atmosphere if necessary to avoid hydrolysis, and use suitable corrosion-resistant containers. Adhere to all relevant chemical storage regulations and safety procedures.
    Application of 4-Chloro-3-Nitrobenzenesulfonyl Chloride

    Applications of 4-Chloro-3-Nitrobenzenesulfonyl Chloride in Industrial Manufacturing

    As the original manufacturer of 4-Chloro-3-Nitrobenzenesulfonyl Chloride, we supply material with certified quality for demanding industrial sectors. Below we outline key downstream application fields, detailing standards compliance, dosage, integration points, and end products.

    1. Synthesis of Pharmaceutical Sulfonamides

    Pharmaceutical producers utilize this sulfonyl chloride as a core reagent for synthesizing sulfonamide intermediates, especially for drugs containing sulfonyl-linked aromatic groups. The material reacts with varied amines to generate essential building blocks for antibacterial therapies and specific enzyme inhibitors. Controlled handling is crucial for reaction selectivity and impurity minimization, with full documentation required for traceability in compliant drug manufacturing environments.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP, EP, JP monographs (where applicable to intermediate standards)
    • 21 CFR Part 211 (cGMP for Finished Pharmaceuticals)
    • REACH registration and documentation for API intermediates (EU)

    Typical usage ratio

    • 1.0–1.15 molar equivalents relative to amine reactants, with adjustment based on substrate reactivity and desired yield

    Downstream process integration

    • Reactant addition stage for sulfonamide bond introduction (batch or continuous reactors)
    • Post-reaction quench and extractive work-up steps to isolate sulfonamide intermediates
    • Integrated in multi-step syntheses leading to small-molecule APIs

    Final product types

    • Sulfonamide-based antibiotics (e.g., sulfadiazine derivatives)
    • Antihypertensive drug precursors
    • Enzyme inhibitor intermediate compounds

    2. Agrochemical Intermediate Production

    Manufacturers in crop protection rely on this sulfonyl chloride as a key functionalization agent for synthesizing selective herbicide and fungicide precursors. The material reacts efficiently with heterocyclic and aromatic amines, facilitating downstream transformations for actives engineered to meet regulatory requirements on residuals and performance. Every batch undergoes contaminant profiling to meet environmental emission standards in regulated markets.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • ISO 9001 certified quality systems
    • Regulation (EC) No 1107/2009 on plant protection product approval
    • EPA Pesticide Registration Guidelines (USA)

    Typical usage ratio

    • 0.9–1.2 equivalents versus aminated substrates; formulation labs optimize ratio for conversion and cost efficiency

    Downstream process integration

    • Sulfonylation steps to introduce electron-withdrawing groups enhancing agro-active stability
    • Integration at mid-stage synthesis prior to final formulation blending and microencapsulation

    Final product types

    • Triazole-based fungicide intermediates
    • Sulfonylurea herbicide precursors
    • Phenoxyacetic acid derivative building blocks

    3. Chemical Protection for Peptide Synthesis (Sulfonylation of Amines)

    In peptide manufacturing, our material functions as a selective amine-protecting group reagent, particularly for specialty peptide and oligonucleotide syntheses. Its distinct sulfonyl chloride moiety ensures rapid and high-yielding protection in the presence of competing nucleophiles, streamlining purification and downstream deprotection steps. Users document risk assessments and cleaning validation for carry-over in regulated synthesis lines.

    Industry compliance standards

    • ICH Q11 (Development and Manufacture of Drug Substances)
    • USP General Chapter <1058> Analytical Instrument Qualification
    • ISO 13485 for medical raw material traceability (where applicable)
    • GMP guidelines for custom peptide synthesis

    Typical usage ratio

    • 1.1–1.3 molar equivalents per amine site, adjusted for substrate sensitivity and sequence length

    Downstream process integration

    • Initial coupling stage for N-terminal amine protection
    • Parallel peptide elongation and side-chain protection/deprotection cycles
    • Final deprotection and product isolation steps

    Final product types

    • Protected peptide fragments
    • Oligonucleotide intermediate building blocks
    • Custom synthetic amino acid derivatives

    4. Dyes and Pigments Synthesis

    Specialty dye manufacturers apply this material as a sulfonylating agent for producing triarylmethane, azo, and anthraquinone dye intermediates. The activated sulfonyl group enhances solubility and facilitates coupling reactions for colorant development under precise process control. QC teams validate batch consistency to support downstream blending and color fastness specifications for textile and ink applications.

    Industry compliance standards

    • Oeko-Tex Standard 100 (for textiles safety)
    • REACH SVHC screening and registration
    • ISO 14001 Environmental Management for effluent control
    • Good Laboratory Practice (GLP) for dye ingredient assessment

    Typical usage ratio

    • 0.8–1.1 mole per coupling substrate, fine-tuned for color strength and purity after lab-scale trials

    Downstream process integration

    • Sulfonylation stage for colorant structure modification
    • Reaction in stirred-tank or continuous flow reactors before precipitation and drying
    • Downstream blending with dispersing agents for pigment formulation

    Final product types

    • Acid azo dyes
    • Reactive dyes for cellulose fibers
    • Anthraquinone-based pigments

    5. Synthesis of Specialty Polymers and Resins

    Industrial polymer and resin producers use this sulfonyl chloride as a monomer modifier and crosslinking agent in high-performance engineering plastics. Its reactive sulfonyl group introduces polarity and functional handles for subsequent chain extension or crosslinking, with process integration tailored for solvent-resistant, thermally stable resin systems. Full raw material traceability supports downstream quality audits.

    Industry compliance standards

    • ISO 9001 Quality Management Systems
    • ASTM D638 (Tensile Properties for Plastics, as relevant for end testing)
    • RoHS 2011/65/EU compliance for electronics parts
    • UL 94 for flame retardancy (where application requires)

    Typical usage ratio

    • 0.5–2.0% by weight in copolymer blends or as specified per polymer batch formulation

    Downstream process integration

    • Functional additive blending during prepolymer formation
    • Post-polymerization sulfonation for end-capping or crosslinking
    • Incorporation with curing or extrusion protocols for tailored resin properties

    Final product types

    • Specialty sulfonated epoxy resins
    • Engineering thermoplastics with enhanced adhesion
    • High-performance coatings and adhesives
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    Certification & Compliance
    More Introduction

    4-Chloro-3-Nitrobenzenesulfonyl Chloride: Practical Value in Sulfonation Chemistry

    Practical Overview From Our Plant Floor

    At our factory, chemical synthesis starts long before any batch is poured into a reactor. Years of experience have shown that no two sulfonyl chlorides are truly interchangeable, especially in fields requiring specific reactivity profiles. 4-Chloro-3-nitrobenzenesulfonyl chloride (model: 99.5% pure, yellow crystalline solid) addresses selectivity needs at a fundamental level. Chemists in pharmaceuticals, agrochemicals, and specialty dye production consistently return to this compound because of its functional group arrangement and stable, isolatable structure. Handling this product every day, we see requests from both research labs and global processing facilities who require confidence in every shipment.

    Every batch that exits our dryers comes from tightly controlled chlorosulfonation routes. The core lies in the one-two punch of a nitro group at the 3-position and chloro at the 4-position. This arrangement steers both the electron density of the aromatic ring and influences how subsequent nucleophilic substitutions take place—no theoretical textbook background can convey the difference that years of trial batches and yield optimization truly reveal. Some customers use it in small scale, seeking precision in step-growth polymers or peptide protection chemistry. Others move toward tonnage quantities, introducing it upstream in multistep syntheses where its robust leaving group properties matter more than anything else.

    Differentiation From Similar Sulfonyl Chlorides

    More general sulfonyl chlorides—such as benzenesulfonyl chloride or toluenesulfonyl chloride—lack the electron-withdrawing power and activation at these specific positions. The difference might not seem dramatic in catalogs but turns unmistakable during downstream reactions. Our 4-chloro-3-nitro analog enables clean conversions, often at lower temperatures and with improved selectivity toward desired products. Workers in the lab and on the line note less byproduct formation on scale-up, especially when dealing with substrates sensitive to ortho and para reactivity drift.

    Across hundreds of campaigns, comparative trials consistently show that process times shorten, and purification burdens ease, when the substituents sit exactly where they belong. A para-positioned chloro and meta-positioned nitro work together, not simply as handles but active directors. This is observable in improved conversion rates for sulfonamides, with fewer walks back to chromatographic columns and a sharper product profile in QC analytics. Direct feedback from partner plants highlights tangible improvements in end-of-line purity and waste reduction—metrics that move the needle for formulators and operators alike.

    Industrial Knowhow in Synthesis and Handling

    Many literature reports gloss over the sheer practicality of handling this sulfonyl chloride on scale. Some alternatives, like 2,4-dinitrobenzenesulfonyl chloride, show unsustainable volatility or odor issues during transfer. Our product holds together—crystalline, with a melting point supporting manageable logistics, whether packed into fiber drums or decanted on lab scales. Those working with less stable sulfonyl chlorides often report increased care with refrigeration; our data logs show this product keeping form and function under standard cool, dry storage. Years in actual transportation and customs clearance reveal that the product ships well, holds shelf-life, and gives plant engineers confidence to plan further downstream.

    From direct practice, inspirited by daily feedback from the filing line, we see that 4-chloro-3-nitrobenzenesulfonyl chloride gives teams a high degree of batch-to-batch reproducibility. The yellow tint makes contamination detection easier during visual checks, which reduces error before it reaches the analytical bench. In small-scale synthesis labs, precise solid dispensation is possible without caking or unmanageable static. That advantage disappears when users shift to softer, oilier sulfonyl chlorides sometimes offered as cut-price alternatives.

    Application Driven by Real Chemical Behavior

    Sulfonamide and sulfonate synthesis top usage requests. We receive consistent orders from peptide chemistry groups and material science developers. In peptide protection, this product’s strongly activating nature enables clean N-terminal protection, giving researchers more flexibility in deprotection step choices. Down on the manufacturing scale, the pattern holds. Where a bottleneck has blocked isolation purity or dragged down conversion yield, switching to this specific compound frequently brings measurable improvements.

    Looking at dyes and pigments, we’ve supported plants that struggled with slow, incomplete reactions when using unsubstituted benzenesulfonyl chloride. The nitro/chloro arrangement delivers a cleaner, more intense color outcome due to minimized over-sulfonation and a sharper attack on target nucleophiles. For agrochemical intermediates, the product stands out when process chemists push hard for low-residue and minimal-waste syntheses—a growing regulatory requirement worldwide. In comparative pilot runs, line teams switch to our product and witness fewer incidents of batch rework or costly emission captures.

    Quality Control and Specification as Lived in Manufacturing

    We specify our 4-chloro-3-nitrobenzenesulfonyl chloride to over 99.5% by weight as standard, using multiple HPLC and titration rounds. Chromatographic data shows that major impurities consistently stay below 0.2%. Our experience teaches that allowing wider purity spreads (common in lower-cost variants) adds risk for downstream users. Fine-tuned process control means no surprises when the material enters a multistep workflow or encounters in-situ generation of related sulfonamides.

    Physical form isn’t just cosmetic. Narrow melting point range means less thermal decomposition on heating. Every time we dry a batch, technicians dial in dryer time and temperature based on real sample feedback. This reduces charring and keeps every sack or drum flowing as it should. Long-term partners report that such standardization reduces recalibration and lets automated dispensing lines run with fewer stoppages. The working environment stays safer and more predictable.

    Environmental and Regulatory Perspective

    Choices made in sulfonyl chloride procurement matter not only for productivity but for compliance too. In many regions, waste minimization and airborne emissions from chlorinated compounds now demand traceability. Our continuous improvement program draws on our in-plant audits, evidence from disposal partners, and the latest import/export standards. That means the 4-chloro-3-nitrobenzenesulfonyl chloride we produce meets tighter residual solvent limits and eliminates buffer agents that might cause headaches in downstream processing or local regulatory reviews.

    Disposal route optimization starts here, at synthesis. We collect and recycle mother liquors, drawing down on external solvent burns and halocarbon emissions. Our isolation technicians work with research chemists to ensure as much crude product is collected from every batch, reducing the off-spec and side-stream waste volumes. This translates directly to end users, who report easier wastewater processing, lowered environmental levies, and better sustainability scores at their facilities.

    Plant managers from user companies have told us that environmental regulators increasingly spot-check for sulfonyl chloride metabolites in effluent samples. The low-impurity profile of our material lets these partners pass spot-checks with minimal intervention. Recent years have brought new scrutiny regarding potential dioxin contamination in certain aromatic sulfonyl chlorides. Here, our in-house purification methods leave no ambiguity: every drum meets current analytical thresholds, validated by third-party and internal monitoring alike.

    Worker Safety and Practical Handling

    Worker safety in our facility goes beyond standard MSDS compliance. Sulfonyl chlorides in general require respect on the line—no shortcuts. By controlling particle size distribution tightly, our operators can perform fast, low-dust transfers, reducing respiratory risk. For teams designing packaging lines, the free-flowing crystalline nature of our sulfonyl chloride minimizes clumping and bridging, which in turn keeps exposure windows shorter at every transfer step.

    Aside from the standard PPE and ventilation, application of closed transfer and dilution procedures has reduced annual incidents by tangible numbers. In real-world use, plant supervisors underline how open handling of cheaper, dustier sulfonyl chlorides posed headaches—frequent spills, eye irritation, and time lost in cleanup. Adopting our product brings down these incident counts, cementing confidence for operators and maintenance crews. Our training team updates handling guidelines regularly, feeding improvements back into our own plant practices.

    Supply Consistency and Real-World Readiness

    Ongoing commitment to uninterrupted supply matters in industries with never-ceasing production schedules. Any bottleneck in sourcing ripples down to scheduling, headcount, and customer commitments. Unlike sporadic importers who rely on fragmented stocks, our facility maintains rolling batch production, supported by on-site storage capacity. Inventory reserves allow us to weather annual plant overhauls or unforeseen raw material delays without leaving our customers in limbo.

    Procurement teams want predictability, especially for critical-path reagents. Our logistics crew plans out scheduled shipments at regular intervals, responding to both contractual forecasts and last-minute pull requests. We operate with advance warning systems calibrated to inventory thresholds tied directly to firm contractual obligations. Long-tenured production planners tell us this steady hand at the tiller gives them freedom to sequence lengthy, complicated syntheses that can’t afford unplanned downtime.

    Trade regulations change with little warning, particularly for reactive intermediates or goods requiring dual-use clearance. On our end, supply chain and compliance specialists stay on top of shifts in export documentation requirements or destination-specific transport certificates. We have the in-house capacity to reroute or relabel in compliance with emerging new standards without pausing deliveries. In our experience, fast pivots like these have prevented multiple customer lines from going idle due to administrative gridlock.

    Reliability in Technical Assistance

    Technical service isn’t an afterthought. We see our role stretching well beyond packing product into drums. When a customer hits a snag—unexpected side reactions, product crystallization issues, or analytical headaches—our process chemists pick up the phone or respond onsite, offering insights rooted in direct plant experience. Such involvement isn’t academic. Many of the optimizations that now feature in our production protocol sprouted from joint troubleshooting fielded at the customer’s reactor, with both their operators and ours documenting observations and improvements.

    Over the years, this open knowledge flow tightened process windows for practically every recurring customer. Our support covers method validation, adjustment of storage and transfer protocols, and even guidance on new applications—especially for teams launching new lines or scaling up laboratory successes to industrial tonnage. The learning runs both ways. Feedback loops from users lead to upgrades in our own in-plant protocols, ensuring continuous progress in quality and usability.

    In niche application sectors—such as custom protective group synthesis—we have worked directly with R&D chemists to guide them away from less suitable, bulkier sulfonyl chlorides when poorer conversions and side reactions slowed their research. By introducing the nitro/chloro variant, these teams reported not only yield improvement but less clean-up work and faster analytical turnaround—freeing up resources and people to move on to other project milestones.

    Supporting Cost Management and Operational Efficiency

    Operational budgets at manufacturing plants seldom leave room for error. Every kilo of starting material that translates to off-spec product represents lost direct material costs, wasted labor hours, and time bottlenecked on clean-up, disposal, and requalification. We structure our quality control not only around purity but also around ease in real-world handling. Our internal cost studies have shown that, despite a slightly higher purchase price, the overall cost per reaction cycle drops as less agent is wasted and overall isolation is more consistent.

    Users with continuous flow systems, as well as those in batch mode, have signaled reduced foil downtime and less frequency in filter cake blockages, owing to consistent physical properties and controlled granulation. The labor savings and smoother campaign durations increase throughput without hidden overheads. Management reviews in customer plants note that this cost containment echoes through to plant output, reduced overtime, and budget predictability on procurement lines.

    For companies answering to environmental auditors and shareholders alike, the reduced waste handling and byproduct formation play key roles in securing audit greenlights and in fending off fines. We work with logistics partners whose last-mile practices have, over time, been tuned to prevent product loss in transit—a not-inconsiderable detail as transportation mishaps contribute to both direct financial and indirect reputational costs. Over many cycles, the full supply chain—from our reactors to a finished downstream product—delivers tighter margins and higher throughput.

    Adapting to Evolving Industry Standards

    The market for sulfonyl chlorides advances with both regulatory pressure and customer demands for higher selectivity and fewer side losses. Not content with “good enough,” we benchmark against new synthetic requirements and peer input. Our investments in process automation and anti-contamination monitoring don’t just fulfill mandates—they build a better, more reliable product over time.

    A shift in the regulatory landscape can redraw the risk map overnight. We keep close tabs on emerging contaminants, proactively update our analytical panel, and align batch documentation with international best practice. Clients seeking ISO-aligned records, enhanced traceability, or custom batch analytics have found our team ready to engage, not only in documentation but in the science behind it.

    On-the-fly adaptation is an asset in chemicals manufacturing. From the earliest days producing small-lot volumes to today’s multi-metric tonnage, our combined lab and plant teams have steered each change in product specification, bringing customer perspectives into process development. The lessons taken from each year of production and every batch shipped feed directly into technical guidelines and upgrade paths.

    Summing Up What Manufactures Value Most

    Through every year of work with 4-chloro-3-nitrobenzenesulfonyl chloride, the same reality asserts itself: the unique arrangement of substituents on its aromatic ring isn’t just a matter of chemical curiosity, but a driver of practical, proven performance in the field. Chemists and process teams rely on this combination to fine-tune reactions, raise yields, and keep production humming. The discipline of our daily routines—planning, synthesis, testing, packing, and technical support—reinforces one point: direct, manufacturable improvements pay off for end users far beyond what a spec sheet alone can relay.

    The future of production in this area will always depend on real evidence from reactors and process lines, not catalog promises or abstracted “industry standards.” Our journey—grounded in trial, feedback, and relentless adjustment—keeps our partners advancing ahead of new regulatory challenges and operational complexities. By hinging our work on real performance, tight process management, and continual engagement, we keep both our lines and those of our customers running with a reliability that meets rising demands for quality and traceability.