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4-Methyl-3-Nitrobenzene-1-Sulfonyl Chloride

    • Product Name 4-Methyl-3-Nitrobenzene-1-Sulfonyl Chloride
    • Alias 4-Methyl-3-nitrobenzenesulfonyl chloride
    • Einecs 256-119-7
    • 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
    VTB
    Specifications

    HS Code

    160057

    Productname 4-Methyl-3-Nitrobenzene-1-Sulfonyl Chloride
    Casnumber 1576-35-8
    Molecularformula C7H6ClNO4S
    Molecularweight 235.64 g/mol
    Appearance Yellow to orange crystalline powder
    Meltingpoint 101-104°C
    Solubility Reactively soluble in organic solvents such as dichloromethane
    Purity Typically ≥98%
    Storageconditions Store in a cool, dry place, keep container tightly closed
    Synonyms 4-Methyl-3-nitrobenzenesulfonyl chloride
    Hazardstatements Causes serious eye irritation; may cause respiratory irritation

    As an accredited 4-Methyl-3-Nitrobenzene-1-Sulfonyl Chloride factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The chemical is packaged in a sealed 100g amber glass bottle with a tamper-evident cap, labeled with proper hazard and handling information.
    Shipping 4-Methyl-3-nitrobenzene-1-sulfonyl chloride is shipped in tightly sealed containers, protected from moisture and light. It requires cool, dry storage and is classified as hazardous; handle with appropriate safety precautions. Transportation follows regulations for corrosive substances, ensuring clear labeling and documentation to prevent accidental release or exposure during transit.
    Storage 4-Methyl-3-Nitrobenzene-1-Sulfonyl Chloride should be stored in a tightly closed container, in a cool, dry, well-ventilated area away from moisture, heat sources, and incompatible substances such as bases and strong oxidizers. Protect from light and avoid humidity to prevent decomposition or hydrolysis. Ensure proper labeling and keep away from direct sunlight and ignition sources. Store under inert atmosphere if possible.
    Application of 4-Methyl-3-Nitrobenzene-1-Sulfonyl Chloride

    Applications of 4-Methyl-3-Nitrobenzene-1-Sulfonyl Chloride in Industrial Manufacturing

    4-Methyl-3-Nitrobenzene-1-Sulfonyl Chloride serves as a specialized intermediate across several high-regulation chemical process industries. Below, we outline its application in authentic industrial tracks, detailing compliance benchmarks, integration points, and typical finished goods seen in downstream manufacturing.

    1. Pharmaceutical Intermediates for Antibacterial Agents

    This material functions as a key sulfonation reagent in the synthesis of select antibacterial sulfonamide APIs. It reacts at the early sulfonation step to create core structures, driving specificity in pharmaceutical syntheses. Strict process controls ensure the absence of unresolved sulfonyl chloride residues, and batch records require precise stoichiometry for regulatory compliance and traceability.

    Industry compliance standards

    • Complies with ICH Q7 Good Manufacturing Practice guidance for active pharmaceutical ingredients
    • Follows US FDA 21 CFR Part 211 for finished pharmaceuticals
    • Adheres to European Pharmacopoeia (Ph. Eur.) quality benchmarks for intermediates
    • Material traceability documented to USP <467> residual solvent limits

    Typical usage ratio

    • Employed at 0.9 to 1.2 molar equivalents relative to primary amine reactant, depending on target molecule and batch scale

    Downstream process integration

    • Added to reaction vessel during initial sulfonation, before amine condensation
    • Integrated with automated dosing systems to prevent operator exposure
    • Batch analytics confirm post-reaction conversion before downstream purification

    Final product types

    • Sulfamethoxazole API
    • Other nitrobenzene-based sulfonamide intermediates
    • Biosynthetic enzyme inhibitors for R&D

    2. Agrochemical Active Ingredient Synthesis

    This compound plays an essential structural modification role in the synthesis of herbicidal and pesticidal active ingredients. Sulfonylation steps introduce key sulfonamide functionalities, which undergo further transformations into highly regulated crop protection agents. All usage and handling follow robust EH&S protocols, with detailed tracking during both pilot and commercial runs.

    Industry compliance standards

    • EPA TSCA Inventory Listing for use in manufacturing substances for US market
    • Compliance with Regulation (EC) No 1107/2009 for plant protection products in EU
    • OHSAS 18001-compliant occupational exposure protocols in handling

    Typical usage ratio

    • Applied at 1.0 to 1.3 molar equivalents per base aromatic precursor, adjusted for process yield and impurity risk

    Downstream process integration

    • Dosage occurs during intermediate-stage sulfonamide group introduction
    • Closed system transfer prevents operator contact with unreacted sulfonyl chloride
    • Downstream process includes neutralization and removal of residual chloride

    Final product types

    • Sulfonylurea herbicide intermediates
    • Nitro-aromatic herbicides and insecticides
    • Fungicide building blocks

    3. Dye and Pigment Intermediate Manufacturing

    The compound acts as a selectivity enhancer and activated group donor within specialty aromatic dye syntheses. It contributes nitro and sulfonyl groups for the preparation of color bodies with improved fastness and distinct chromophores. Careful metering and downstream neutralization are necessary to eliminate reactive residues in high-purity pigment precursors.

    Industry compliance standards

    • Adheres to REACH Annex XIV and XVII restrictions for aromatic amines
    • Complies with ETAD Code of Practice for dye and pigment safety
    • Consistent with ASTM D3135 standards for dye material quality

    Typical usage ratio

    • Used at 0.8 to 1.05 molar equivalents relative to coupler base, based on final chromophoric requirements

    Downstream process integration

    • Charged to colorant precursor tanks under inert atmosphere conditions
    • Reacts at mid-point of multi-step dye synthesis, usually pre-coupling
    • Post-reaction process includes full work-up to reduce residual sulfonyl chloride to below 10 ppm

    Final product types

    • Azo dye intermediates for textile applications
    • Specialty pigments for plastics and inks
    • Reactive dye precursors for fiber processing

    4. Specialty Polymer Crosslinking Agent

    It serves as a sulfonating and functional crosslinking agent in custom-engineered specialty polymer backbones, especially for ion-exchange and filtration membrane production. It directly modifies aromatic chains and delivers highly selective ionic functionalities, which influence end-use mechanical and performance properties. This role requires inline monitoring to avoid crosslink density variation.

    Industry compliance standards

    • Meets ISO 9001:2015 requirements for quality management systems in advanced polymer production
    • Compliant with FDA 21 CFR 177.1520 for indirect food contact in membranes
    • Conforms to RoHS Directive for restriction of hazardous substances in electronics filtration membranes

    Typical usage ratio

    • Ranged between 0.03 to 0.15 parts by weight per 100 parts of polymer resin, dosing tuned for desired ionic exchange capacity

    Downstream process integration

    • Dispensed during final polymerization phase or cast in situ before membrane extrusion
    • Subjected to full thermal curing and post-crosslink extraction
    • In-line FTIR or titrimetric analysis verifies incorporation rate

    Final product types

    • Cation- and anion-exchange membranes
    • Battery separator films
    • Specialty polymer beads for water treatment

    5. Protecting Group Reagent for Organic Synthesis

    The compound finds use as a sulfonylating agent for the introduction of robust protection groups on amines and alcohols in complex multi-step organic syntheses. It is selected for its reactivity and unique electron-withdrawing properties, allowing for later deprotection under controlled conditions. Analytical techniques confirm complete removal of protecting group to satisfy high-purity synthetic standards.

    Industry compliance standards

    • Compliant with ISO 13485 for life science fine chemical production
    • Follows GLP (Good Laboratory Practice) for synthetic development workflows
    • Abides by internal QA release testing according to customer-dictated monograph

    Typical usage ratio

    • Typically 1.0 to 1.15 equivalents per nucleophilic site; fine-tuned to avoid excess unreacted sulfonyl chloride

    Downstream process integration

    • Introduced in controlled batch mode at primary or secondary amine protection stage
    • Followed by aqueous work-up and purification chromatographic separation
    • Subsequent steps include planned deprotection under mild or reductive conditions

    Final product types

    • Intermediate building blocks for complex API synthesis
    • Sulfonamide-protected amino acids
    • Advanced organic molecules for combinatorial chemistry libraries
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    Certification & Compliance
    More Introduction

    4-Methyl-3-Nitrobenzene-1-Sulfonyl Chloride: A Featured Intermediate from Our Manufacturing Lines

    Shaping Chemical Synthesis and Downstream Value Addition

    Every day at our manufacturing site, hundreds of drums are filled with intermediates that drive new chemistry in pharmaceuticals, agrochemicals, and specialty chemicals. One product that we see move from the reactor to the warehouse and onto a growing list of customer formulations is 4-Methyl-3-Nitrobenzene-1-Sulfonyl Chloride. We manufacture this compound through a multistep process, controlling conditions to achieve key purity and performance parameters. The bright yellow crystalline powder, catalogued as 4-Methyl-3-Nitrobenzene-1-Sulfonyl Chloride, brings well-recognized functionality for introducing sulfonyl chloride groups into aromatic molecules, a crucial transformation in advanced chemical synthesis.

    Day in, day out, we weigh, pack, and quality-test this compound ourselves, confirming through spectral and chromatographic analysis that it meets the benchmarks demanded by innovators and production chemists. Our batches maintain a high degree of chemical purity, with minimal presence of unreacted starting materials and related impurities. For customers, this translates to fewer downstream purification steps and consistent yields, supporting scalable, cost-effective reactions at multi-kilogram or multi-ton levels. Through our viewpoint as the actual producer, we recognize that quality directly influences success in the final application, and we reinforce every lot with documentation drawn right from our labs—not someone else’s phrasebook.

    Where 4-Methyl-3-Nitrobenzene-1-Sulfonyl Chloride Meets Real-World Chemistry

    Sulfonyl chlorides such as this one have a reputation among process chemists as versatile electrophiles. The chemical backbone—a methyl group at the para position, the nitro substituent at meta, and the sulfonyl chloride at ortho—allows the molecule to activate nucleophilic aromatic substitution for novel derivatives. Our customers employ this compound for introducing protective sulfonyl groups on amines or alcohols, for building blocks in active pharmaceuticals, and for customizing complex dye intermediates. In our own pilot applications, we have used it to synthesize sulfonamides, which later became key fragments in lead drug candidates.

    Compared to unsubstituted benzenesulfonyl chloride, the presence of both methyl and nitro groups raises the electron deficiency of the aromatic ring, enhancing the reactivity of the sulfonyl chloride. The nitro group directs substitution toward para or ortho positions, creating more controlled reaction patterns, which reduces unwanted byproducts. Our production team regularly monitors reactivity with test nucleophiles to ensure consistent batch behavior, and we maintain a reliable log of outcomes that we use for both internal process improvements and direct consultation with long-term clients.

    Safety remains central as we handle large volumes of this compound. We train staff to manage the reactive sulfonyl chloride group, which, under the wrong conditions, can release corrosive hydrochloric acid. Our facility minimizes exposure with sealed handling systems and redundant containment. Every shipment leaves our plant after a final inspection—color, melting point, and purity all must clear the mark, or the batch is cycled for reprocessing. Having full control over the manufacturing chain, from raw material selection, to reactor sequencing, to the final drum inspection, allows us to guarantee what we ship each time. This level of confidence simply doesn’t come from outsourcing or reselling.

    Inside the Manufacturing Workflow: Managing Quality Day to Day

    Sourcing pure toluene derivatives, nitrating under precisely controlled acid concentrations, isolating and drying the sulphonic acid, then chlorinating with high-purity reagents—each step builds on the previous one, demanding attention to reagent quality and real-time adjustments. As producers, we know cut corners at any stage come back to haunt the final product, so we invest in hands-on monitoring and traceability. Automation in weighing, addition sequences, and mixing regimes improves reproducibility, but experienced staff still sign off on key transitions.

    No shipment leaves untested. Our routine includes HPLC and NMR analysis to spot even minor impurities. We sometimes discover byproduct formation that requires a process tweak, and those lessons turn into new SOPs for future batches. By handling all reprocessing in-house, we can recover valuable out-of-spec material and keep waste limited. Clients regularly request samples for new processes or formulations, and we support trial runs by providing technical background gathered from our own production and testwork. This supporting data comes from direct handling—not rebranded documents.

    As an established manufacturer, audit visits are part of our regular schedule. We hold years' worth of batch records and testing data to give full transparency, and we provide open access to our manufacturing flow for qualifying chemists who want to understand the origins of what will become a new pharmaceutical, agrochemical or specialty polymer. In every case, long-term partnerships start with proof that we control every part of the process, not just the paperwork.

    Comparing with Other Sulfonyl Chlorides and Nitro Derivatives

    Clients often ask how 4-Methyl-3-Nitrobenzene-1-Sulfonyl Chloride compares to benzenesulfonyl chloride or other nitrobenzenesulfonyl chlorides. Based on years of feedback and our own application testing, the dual substitution by methyl and nitro groups shifts the product’s reactivity and solubility. The methyl group increases hydrophobicity, helping with organic-phase processing, while the nitro group tunes the ring for selective nucleophilic substitution. End-users report higher selectivity and fewer byproducts in certain sulfonamide syntheses compared to using unsubstituted benzenesulfonyl chloride or the 4-methyl variant alone.

    Subtle differences in melting point, physical form, and hygroscopicity arise from these chemical changes. We see the nitro-methyl combination raise the melting point, offering easier downstream handling and storage in environments prone to temperature swings. The crystalline material stays free-flowing under standard warehouse conditions as long as containers are kept tightly sealed, a practical benefit for both our logistics team and the customer’s receiving staff. While the sulfonyl chloride group remains equally reactive toward nucleophiles across this class of chemicals, the particular substitution pattern can significantly reduce unwanted oligomerization or side-chain formation—a difference that matters when scale-up moves from milligrams to multi-kilogram lots.

    Another aspect: some nitrobenzenesulfonyl chlorides from other suppliers display variable color and levels of carbonaceous impurity if not properly purified. Through years of refining our process, we've learned to remove persistent impurity profiles, resulting in bright, consistent product color and minimized decomposition during storage. Our technical staff support inquiries with data from actual production lots, not only literature references. This close link between process knowledge and end-user requirements helps resolve points of difference and leads to more reliable sourcing compared to purely trading-driven channels.

    Real-World Challenges: From Manufacturing to End Use

    Scaling up this compound takes more than batch scheduling. As demand shifts upward, raw material sourcing becomes critical. Our procurement team builds in buffer inventories for the key precursors—methylated toluenes, high-purity acid, chlorine donors—drawing on trusted supply partners with long-standing relationships. Disruption in one source can ripple through the whole chain, pushing us to forecast demand with both short-term and longer-term outlooks. We establish alternate routes and evaluate pricing monthly, resulting in better stability for customers who need forward contract consistency.

    Chemical intermediates such as this present their share of shipping and regulatory challenges. The sulfonyl chloride group requires compliance with hazmat protocols, and the nitro group flags extra attention at customs. Our shipping team stays current with international transport regulations and adapts methods for each region. For locations with strict regulatory review, we supply full composition data and documented production records, helping customers clear hurdles at the point of import.

    Handling hazards in the plant stays front-of-mind. Workers undergo training on every new SOP related to sulfonyl chloride storage and transfer. We invest in full personal protection, negative-pressure containment, and emergency planning with local responders. Since the nitro group has the potential for exothermic decomposition under high temperature, monitoring and process safeguards remain active during isolation and packaging. By keeping all manufacturing, packaging, and QA internal, we have tight control over material outflow—no relabeling, no gaps in the supply chain, and no guessing at product provenance.

    Adapting to Customer Needs, Not Just Batch Outputs

    Clients developing new syntheses for active pharma ingredients or fine chemicals often raise questions straight to our process team. They dig into sulfonylation conditions, compatibility with varied solvents, and downstream workup requirements. Our technical group draws on practical experience—what works at lab scale can go sideways on kilo-plant runs if byproduct profiles shift or solubility changes. We exchange data from our own attempts, noting what variables yield sharper transitions, cleaner separations, or faster filtrations. Sometimes we adjust particle size distributions at the drying stage, or even tailor bulk packaging, to ease transfer and minimize dust. This level of responsiveness emerges only through direct production insight, not abstract product bullet points.

    Process troubleshooting forms much of our day-to-day client interaction. If a customer encounters inconsistent sulfonamide purity or unexpected isomer formation, we analyze not just their submitted samples but also review our manufacturing logs for possible batch-specific patterns. Our accumulated knowhow bridges information gaps between synthetic literature and the reality of industrial-scale transformations. We regularly update batch recommendation sheets and share our validated findings, which helps customers avoid common pitfalls that can tack days or weeks onto their development timelines.

    We have seen customers switch from other suppliers' products because of recurring variability in melting point, solubility, or reactivity. Having direct access to our reactor data, we can trace every lot to its formative conditions. If a run diverges from the norm, we note it and investigate, feeding improvements straight back into the workflow. Years of iterative tuning create not only a physical product, but also a technical repository to support high-stakes project work among process development teams. For buyers, reliability comes not just from what’s in the drum, but from open access to the manufacturing reality behind it.

    Continuous Improvement and Targeted Innovation

    Staying current means refining both process and product. Our production chemists and engineers test alternative reagents, optimize waste streams, and trial energy-saving process adjustments. We investigate modifications aimed at increasing throughput without sacrificing batch-to-batch purity. Sometimes small tweaks in temperature profiles or raw material purification eliminate recurring issues, an outcome visible only through years of hands-on metrics gathering. This drive for refinement helps keep costs reasonable and lead times short, benefiting end-users who value supply stability.

    From time to time, customers ask about greener chemistry alternatives or reduced energy usage in the sulfonation and chlorination steps. We track industry moves toward lower-waste and energy-conserving processes, evaluating new catalysts or recyclable solvents in pilot-scale lots before regular production shifts. Our team communicates back findings—where environmental gains align with product integrity, we integrate those improvements. In some cases, we have incorporated waste heat recovery and solvent recycling that cut the environmental burden for every batch shipped.

    As direct manufacturers, safety, quality, and predictability remain our highest standards. We engineer our processes not just to meet minimum compliance, but to create long-term partnerships where customers are empowered to innovate on a reliable substrate. Clients launching products into regulated markets—pharmaceutical or agrochemical—depend on unwavering purity and batch-to-batch traceability. By holding every major lever in the hands of our own people, and offering technical support that stems from firsthand experience, we anchor our reputation in concrete, explained actions.

    Looking Forward with Application-Driven Collaboration

    The field is moving fast, from small-molecule APIs to high-performance polymers and dyes. We dedicate time and resources to staying ahead of new regulatory guidance, handling hazard communication, and improving documentation. Yearly customer audits deepen the trust that comes from transparent process sharing. Beyond standard supply, we offer our plant as a pilot resource for clients scaling up or validating new applications. Our analysts and chemists provide not only QC documentation, but in-depth guidance based on production records and prior troubleshooting.

    The more our partners understand the actual origins and behaviors of 4-Methyl-3-Nitrobenzene-1-Sulfonyl Chloride, the less guesswork affects downstream innovation. We find customers value practical advice even more than the physical product—timelines shorten, failures drop, and developmental risk goes down. Direct manufacturing gives us both the authority and the insight to fill that role. Whether a new pharmaceutical candidate or a specialty material is the goal, our compound moves forward with transparency and traceable quality, every single time.

    Summary of Practical Product Value

    The unique substitution pattern on our 4-Methyl-3-Nitrobenzene-1-Sulfonyl Chloride supports greater control and predictability in challenging chemical syntheses. By controlling production from start to finish, minimizing impurities, and engaging personally with each customer's technical goals, we create more than a product on a shelf—it becomes a platform for reliable, efficient process development across sectors. Our team’s own experience sets the tone for a supply relationship based on shared progress, and the compound’s continual role in new chemistry proves its place as a vital intermediate for today’s innovators.