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M-Toluenesulfonyl Chloride

    • Product Name M-Toluenesulfonyl Chloride
    • Alias Tosyl chloride
    • Einecs 204-483-3
    • 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

    856130

    Chemical Name M-Toluenesulfonyl Chloride
    Other Names 3-Methylbenzenesulfonyl chloride
    Chemical Formula C7H7ClO2S
    Molecular Weight 190.65 g/mol
    Cas Number 98-59-9
    Appearance White to off-white crystalline powder
    Melting Point 65-69 °C
    Boiling Point 144 °C (at 20 mmHg)
    Density 1.32 g/cm3
    Solubility Slightly soluble in water; soluble in organic solvents like chloroform and ether
    Odor Pungent
    Refractive Index 1.586
    Flash Point 160 °C

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

    Packing & Storage
    Packing M-Toluenesulfonyl Chloride is packaged in a 500g amber glass bottle, tightly sealed, with hazard labeling and product identification.
    Shipping M-Toluenesulfonyl Chloride should be shipped in tightly sealed, corrosion-resistant containers, protected from moisture and incompatible substances. It must be clearly labeled as hazardous, following DOT, IATA, or IMDG guidelines, and handled by trained personnel using appropriate protective equipment. Store and transport in a cool, well-ventilated area away from heat sources.
    Storage M-Toluenesulfonyl chloride should be stored in a cool, dry, and well-ventilated area, away from heat, moisture, and incompatible substances such as strong bases and oxidizers. Keep the container tightly closed and protected from direct sunlight. Store in a corrosive-resistant, labeled container, and avoid exposure to air and humid conditions to prevent hydrolysis and hazardous byproduct formation.
    Application of M-Toluenesulfonyl Chloride

    Applications of M-Toluenesulfonyl Chloride in Industrial Manufacturing

    M-Toluenesulfonyl Chloride has established its position as a key intermediate in multiple industrial sectors. Our production and supply are aligned with strict downstream demands in organic synthesis, API precursor manufacturing, agrochemical intermediates, specialty polymer modification, and advanced materials synthesis. The following applications reflect real-world deployment in regulated, high-volume industries.

    1. Pharmaceutical Intermediate Manufacturing

    This material serves as an essential sulfonylating agent and leaving group provider in the synthesis pipeline for active pharmaceutical ingredient (API) precursors. Its use manifests most frequently in N-alkylation reactions, protecting group strategies for amines and alcohols, and preparation of tosylates that become key intermediates for cardiovascular, anti-infective, and central nervous system pharmaceutical classes. Manufacturing lines for sulfonamide antibiotics and certain anti-hypertensive molecules utilize this compound during critical multi-step synthesis, with rigorous impurity control managed under cGMP scrutiny.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • WHO GMP for Pharmaceutical Production
    • US Pharmacopoeia (USP) relevant monographs for intermediates
    • European Pharmacopoeia (Ph. Eur.) guidelines regarding process impurities

    Typical usage ratio

    • 0.8–1.2 molar equivalent relative to nucleophile substrate; stoichiometric adjustments based on batch purity and process yield targets

    Downstream process integration

    • Introduced after initial substrate formation as sulfonylation reagent in batch or semi-continuous stirred tank reactors, with isolation and purification steps preceding downstream API transformations

    Final product types

    • Antihypertensive precursors (e.g., tosylated alkylamines)
    • Sulfonamide-based antibiotic intermediates
    • Central nervous system agent scaffolds
    • High-purity protecting groups for peptide synthesis

    2. Agrochemical Synthesis

    The compound enables production of sulfonylurea and sulfonamide herbicides, fungicides, and plant growth regulators. These uses focus on selective functionalization, where controlled reactivity minimizes byproduct formation. Synthesis of chlorsulfuron, metsulfuron, and related herbicide families leverages the reactivity profile for constructing critical heterocyclic sulfonyl components that become part of active pesticide frameworks. Reliable reactivity and cost-controlled supply are essential for scaling production in accredited agrochemical factories.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • ISO 9001:2015 Quality Management (for technical grade raw materials)
    • China National Standard GB/T 16631 Agrochemical Production Regulations
    • REACH Registration, Evaluation, Authorisation and Restriction of Chemicals (for EU export)

    Typical usage ratio

    • 0.9–1.1 molar equivalent per targeted heterocyclic substrate; adjusted for downstream yield and side reaction suppression in pilot and commercial synthesis

    Downstream process integration

    • Blended in main synthesis step to install sulfonyl functional group on core structure after initial ring construction, followed by neutralization and liquid-liquid extraction to isolated active ingredient

    Final product types

    • Sulfonylurea herbicide intermediates
    • Sulfonamide fungicide precursors
    • Plant regulator additive intermediates
    • Precursor components for novel crop protection molecules

    3. Dye and Pigment Manufacturing

    The material provides sulfonyl chlorides required for synthesis of reactive dyes and advanced pigment additives. Key use cases involve functionalizing aromatic amines to create water-soluble dyes and pigment modifiers. These derivatives deliver improved fixation to fibers and better washfastness in textile applications. The sulfonylation reaction enables precise modification of chromophores, facilitating batch-to-batch reproducibility in large-scale dye mills where quality uniformity is regulated by export standards.

    Industry compliance standards

    • OEKO-TEX Standard 100 (for textile dye final products)
    • ISO 14001:2015 (environmental management in chemical dye plants)
    • ZDHC Wastewater Guidelines for Dye Manufacture
    • REACH Annex XVII Restrictions on Azo Dyes (Europe)

    Typical usage ratio

    • 1.0–1.3 molar equivalent per amine or hydroxyl substrate; depends on targeted color fastness and bath scale

    Downstream process integration

    • Added directly as a sulfonylation agent during chromophore coupling; followed by neutralization, filtration, and spray drying or granulation depending on end-use format

    Final product types

    • Reactive fiber dyes (cotton, wool, viscose)
    • Sulfonated pigment additives for inks
    • Specialty dyes for paper and leather finishing
    • Colorant intermediates for polymer masterbatches

    4. Polymer Modification and Advanced Material Additives

    The raw material acts as a functionalizing agent in producing specialty polymers and engineering plastics with targeted thermal or mechanical properties. Sulfonyl chloride groups introduced onto polymer backbones or side chains deliver enhanced solubility, improved processability, and modified interfacial behavior for high-value composites and electronic materials. Batch operations in polyimide, polycarbonate, and specialty polyester synthesis use it for final-stage functional group grafting. Controlled addition is necessary to ensure uniform functionalization and consistent polymer performance parameters.

    Industry compliance standards

    • ASTM D4000 Standard Classification for Polymers
    • ISO 9001:2015 Quality Management for Polymer Processing
    • RoHS Directive 2011/65/EU (for electronics materials)
    • UL 94 Flammability Standards (for some application types)

    Typical usage ratio

    • 0.3–2.5 wt% related to total polymer matrix, dosage optimized for targeted functionalization density and mechanical property requirements

    Downstream process integration

    • Dosed during compounding or post-polymerization functionalization stage, often in twin-screw extruders or reactor vessels with in-line monitoring of modification level

    Final product types

    • High-performance polyimides with sulfonate side chains
    • Modified engineering thermoplastics for electronics
    • Surface-active polymer additives for composite materials
    • Polyester resins for specialty coatings and films

    5. Organic Synthesis for Fine Chemicals

    In integrated fine chemical plants, M-Toluenesulfonyl Chloride acts as a reliable sulfonating and activating agent for diverse transformation reactions. Chemists employ it in batch and flow systems to prepare alkyl and aryl tosylates—key building blocks for further substitution, elimination, and cross-coupling chemistry, especially in high-value custom molecule synthesis. Its consistent reactivity profile enables process intensification in multi-step synthesis sequences, directly impacting throughput and product isolation protocols, especially for export-oriented custom manufacturing contracts.

    Industry compliance standards

    • ISO 9001:2015 Quality Systems for Fine Chemicals
    • Responsible Care® (chemical manufacturing code of practice)
    • REACH compliance for export to EEA markets
    • Process Safety Management (local OSHA or equivalent)

    Typical usage ratio

    • Equimolar to up to 1.5 molar equivalent relative to substrate; carefully calculated by process chemists based on desired selectivity and byproduct minimization

    Downstream process integration

    • Fed into reaction flasks post raw material charging in sulfonation step, monitored by in-process controls (HPLC, GC) to track conversion prior to downstream purification and isolation

    Final product types

    • Specialty alkyl and aryl tosylate intermediates
    • Cross-coupling partners for advanced organic synthesis
    • Activated substrates for contract-manufactured custom molecules
    • Base materials for flavor, fragrance, and specialty monomers
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    Certification & Compliance
    More Introduction

    M-Toluenesulfonyl Chloride: A Chemical Manufacturer’s Perspective

    Our Experience with M-Toluenesulfonyl Chloride

    Every batch of M-Toluenesulfonyl Chloride from our plant carries years of chemistry experience. Chemists on our team have become deeply familiar with this compound, both its production challenges and its growing range of applications. Unlike third-party resellers or brokers, we work directly with raw toluene, monitor every phase of sulfonation and chlorination, and finish with a product that meets the consistently stringent expectations of process chemists around the world. This hands-on approach gives us the knowledge and control to adjust specifications close to the needs of downstream users, particularly in pharma and industrial synthesis.

    Focus on Purity and Consistency

    Our process for M-Toluenesulfonyl Chloride, known in the lab as p-Tosyl Chloride or TsCl, has evolved alongside industry requirements for cleaner reactions and fewer byproducts. Control over raw material purity matters. We dedicate resources to source toluene that is not only technically suitable but also yields less side-product during final chlorination. Over the years, even small improvements at this stage have led to steadier yields and a reduction in hydrolysis byproducts. Typical specifications from our lot analyses range in the high nineties for assay and limit moisture well below what we once thought practical. Final product appears as white or off-white crystalline powder, with melting point checked batch-by-batch, signaling the absence of residual solvents and heavy impurities.

    Why M-Toluenesulfonyl Chloride Matters in Synthesis

    You won’t find many compounds as reliable for the introduction of the tosyl group. Its role in transforming primary and secondary alcohols into good leaving groups—making way for nucleophilic substitution—often gets taken for granted. Veteran process engineers know that a poorly made tosyl chloride, with slightly excessive free acid or moisture, sets off chain reactions involving hydrolysis and loss of yield. In our plant, monitoring dryness and residual acid allows for smooth reactions, reduced post-processing, and gives R&D chemists peace of mind when scaling up. Downstream users depend on these details to keep reaction kinetics predictable and avoid surprises in pilot or commercial runs.

    Model, Grade, and Production Capacity

    We operate a continuous batch reactor capable of producing M-Toluenesulfonyl Chloride at scale, adapting to demand surges in fine chemicals, intermediates, and specialty reagents. While our common model centers on industrial grade, feedback from the pharmaceutical sector helped us refine a higher purity variant, with narrower impurity bands and lower water content. The pharmaceutical grade material stands out in analytical checks, typically favored where mass balance matters most and regulatory filings require batch traceability. Our scale allows for flexibility, adjusting to different production cycles, which sometimes span thousands of tons per year or shift to smaller, more frequent campaign runs for priority orders.

    Handling and Storage Observations

    Toluenesulfonyl chlorides always call for careful storage. Moisture reaction remains the strongest source of decomposition, forming hydrochloric acid and regenerating toluenesulfonic acid. From experience, we know humidity in a warehouse—even at tolerable levels—leads to product caking and sometimes clumps that don’t break down even with rigorous milling. By keeping drums tightly sealed and using moisture barrier liners, we keep these issues under control. Users downstream appreciate this attention to packing detail because it translates directly to easier dissolution and a cleaner transfer of material into reactors. We see less waste, easier material handling, and fewer complaints about harsh odors or unexpected discoloration.

    Key Differences Between Our M-Toluenesulfonyl Chloride and Similar Products

    Chemists often ask how our M-Toluenesulfonyl Chloride sets itself apart from similar chlorosulfonates or alternate leaving group reagents. The most visible difference comes from purity and stability. Unlike cheaper analogues sometimes flooded into the market, our product goes through multi-stage recrystallization and filtering. Free acid content stays comfortably low, which matters for clean substitution reactions. The color stays bright and uniform instead of the yellowish tinge found in some industrial material, especially if synthesized quickly or stored improperly.

    Comparison with benzenesulfonyl chloride or naphthalene-derived sulfonyl chlorides also reveals the versatility of M-Toluenesulfonyl Chloride. Its milder reaction profile produces fewer exotherms and side reactions in our bench and pilot scale feedback, making it more compatible for sensitive organic syntheses. Some clients, experimenting with microwave-assisted or combinatorial methods, report improved yields and easier work-up using our tosyl chloride instead of alternatives with more cumbersome impurities or byproduct profiles.

    Production Challenges and Practical Solutions

    Every year delivers its share of surprises at scale. Production remains sensitive to shifts in upstream supply chain quality, changes in environmental regulations, and ongoing worker safety concerns. Some years, batches show fluctuating yields due to toluene contamination or shifts in sulfonation catalyst efficacy. We invested in inline monitoring—not just to satisfy compliance but to identify upsets quickly. Installations of vent scrubbers and upgraded sampling stations cut down cases of uncontrolled off-gassing, keeping operators safe and limiting the risk of HCl inhalation incidents. Regular training and strong oversight ensure the team keeps up with the hazards, especially when dealing with the exothermic steps of sulfonation and chlorination.

    Moisture has always played the spoiler if not controlled precisely. Applications requiring high-performance output rely on ultra-dry tosyl chloride; we added an extra drying phase and installed automated packing lines under nitrogen purge. These practices increased costs marginally but kept overall customer complaints down. Less compromised product means lower frequencies of shipment returns or complaints over material flows. The learning curve in getting these steps right has been long, but direct involvement on the production floor taught us where shortcuts don't pay off and how to minimize batch-to-batch shifts.

    Feedback Loops from Users

    Veteran process chemists in pharmaceuticals and agrochemicals remain demanding when it comes to sulfonyl chlorides. Over the years, user feedback guided us to adjust different process steps, especially during scale-up. Major multinational buyers provided direct insight into which impurity profiles created issues in continuous reactors or multi-step syntheses. One notable change involved shifting to a two-stage purification, which provided a tighter control over ortho-isomer content and diminished risks of downstream discoloration or odors.

    In fine chemical settings, bench chemists told us small changes in lot color predicted how troublesome a run might become. Whenever off-colors appeared, we've flagged those lots for more extensive analytics. On occasion, a decision to delay a shipment proved wiser than risking a customer's formulation. These experiences underscored a core principle: the people using the material understand its nuances best, and routine lab analytics pays off in fewer disruptions later.

    The Role of M-Toluenesulfonyl Chloride in Research and Manufacturing

    Academic groups and industrial innovators alike continue to find new uses for tosyl chloride. A classic in the chemistry toolkit, it resurfaces repeatedly in patents and journal publications for its versatility. The compound’s ability to activate hydroxyl groups in biomolecules, enable nucleophilic substitutions, and act as an intermediate in dye and plastic manufacturing speaks to how well industrial chemistry adapts established reagents to new challenges. Adoption in peptide synthesis, the manufacture of sulfonated polymers, and selective protection strategies depends not only on chemical reactivity but on how reliably the manufacturer supplies and documents their product.

    Research requests for smaller batches often arrive with tighter demands— NMR purity, heavy metals, and absence of trace amines. Our ability to accommodate such requests results from both scale and willingness to adjust procedures. Larger enterprise buyers tend to focus on cost-effectiveness and bulk availability. In recent years, higher interest in continuous and automated chemistry encouraged us to further refine bulk handling. Our team worked closely with these users, improving packaging—opting for lined drums and custom valve systems—to prevent contamination, keep air out, and make transfers safer and smoother.

    Supporting Sustainability in Production

    As global expectations rise regarding environmental practice, we faced pressure to reduce the footprint of our operations. Chlorosulfonyl chemistry demands rigorous pollution abatement, both for air and liquid emissions. We’ve installed state-of-the-art scrubbers in exhaust lines and invested in water treatment infrastructure that absorbs residual chlorides. Our operations shifted to minimize solvent losses, reclaiming purified toluene and recycling within permissible limits. These efforts reduced raw material waste and have helped bring overall emissions down.

    We hold ourselves responsible for responsible handling, especially for chlorinated byproducts and process residues. Local communities measure chemical plants by their stewardship, so we have built transparency and compliance into day-to-day routines. Our batch release reports frequently feature environmental compliance parameters alongside product specs, and audits provide reassurance that hazardous byproducts don’t simply move downstream or offshore.

    Market Trends and Demand Fluctuations

    Customer demand for M-Toluenesulfonyl Chloride tracks broader economic and regulatory shifts. In years when pharmaceuticals, specialty chemicals, and advanced materials see investment, our production line stretches to keep up. New entries in API production or agrochemical active manufacturing push for tighter specs and higher volumes. International shipping challenges and container shortages now shape delivery timelines more than ever. Direct production lets us adjust quickly, but external bottlenecks—port congestion, import restrictions, and certification updates—require communication and backup planning.

    Pricing pressure exists as always with bulk chemicals, but quality never takes a backseat. We commit to maintaining standards and rarely undercut process integrity for volume alone. Times when low-priced imports of dubious provenance reach the market, we field more inquiries about root causes of failed reactions or surprising analytical results. Our response remains rooted in sharing data, letting prospective customers test our batches in their processes, and being available for troubleshooting—not just pushing a generic spec sheet.

    Commitment to Transparency and Collaboration

    One fact has not changed after years in the chemical manufacturing sector: transparency makes for longer, more productive partnerships. Our production logs are open to review, and we hold current samples from every lot for retrospective analysis. When international customers carry out audits or request COAs, the same lab procedures apply as those used for internal release, never a “special” path just for appearances. This approach resonates with research buyers, regulatory teams, and QC managers on every continent.

    Direct technical dialogue between our chemists and users eliminates a lot of friction when questions arise about reactivity or analytical findings. We approach audits, site visits, and specification development with openness, recognizing chemistry at this level functions across language, regulatory, and industry divides. Questions about unusual impurities, residue reactivity, or blending with other reagents usually get answered without delay—upstream and downstream teams working in sync limit misunderstandings and wasted effort.

    Continuous Improvement and Looking Ahead

    Each year brings new regulatory rules, technological upgrades, and unexpected market demands. Our team tracks changes in global pharmacopeia and technical literature, adapting product and documentation as needed. Customers expect access to up-to-date compliance declarations and new developments in best manufacturing practices. Digital upgrades—real-time batch tracking, connected QC analytics, and more automated handling—gradually become part of every order and shipment.

    Collaborations with university researchers and multi-national labs push us to innovate outside traditional areas. These collaborations highlight new application fields for M-Toluenesulfonyl Chloride, requiring product that meets not only chemical but also safety and environmental management standards. As demand forecasts shift and new downstream processes turn up, our commitment stays with providing reliable, clear, and practical solutions—always with respect for the chemist at the bench and the community around the plant.

    Final Thoughts from the Production Floor

    Producing M-Toluenesulfonyl Chloride connects decades of chemistry knowledge with an outlook shaped by global supply chains, environmental standards, and the relentless curiosity of researchers and manufacturers. Our team values feedback above all, responds to real-life challenges at scale, and stays dedicated to making each batch more reliable than the last. M-Toluenesulfonyl Chloride isn’t just another entry in the chemical catalog; it represents a living collaboration between every manufacturer, chemist, and researcher who touches it, all working to move science and industry forward, one clean reaction at a time.