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4-Chloro-3-Sulfamoylbenzoyl Chloride

    • Product Name 4-Chloro-3-Sulfamoylbenzoyl Chloride
    • Alias 4-Chloro-3-sulphamoylbenzoyl chloride
    • Einecs 407-720-0
    • 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
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    Specifications

    HS Code

    613357

    Product Name 4-Chloro-3-Sulfamoylbenzoyl Chloride
    Cas Number 118344-26-4
    Molecular Formula C7H5Cl2NO3S
    Molecular Weight 270.09 g/mol
    Appearance White to off-white solid
    Purity Typically ≥98%
    Solubility Soluble in organic solvents such as dichloromethane
    Smiles NS(=O)(=O)c1cc(c(cc1)Cl)C(=O)Cl
    Inchi InChI=1S/C7H5Cl2NO3S/c8-5-1-2-6(7(9)11)4(3-5)14(10,12)13/h1-3H,(H2,10,12,13)
    Storage Temperature 2-8°C
    Synonyms 4-Chloro-3-sulfamoylbenzoyl chloride; NSC 759700

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

    Packing & Storage
    Packing 250g amber glass bottle with a tight-sealed cap, labeled with hazard symbols, product name, CAS number, and handling instructions.
    Shipping 4-Chloro-3-Sulfamoylbenzoyl Chloride is shipped as a hazardous chemical. It must be packed in tightly sealed containers, clearly labeled, and transported under dry, cool conditions. Handling and shipping should comply with relevant regulations, such as DOT, IATA, and IMDG, due to its potential corrosive and reactive properties.
    Storage Store **4-Chloro-3-Sulfamoylbenzoyl Chloride** in a tightly sealed container under a dry, inert atmosphere (such as nitrogen or argon) in a cool, well-ventilated area away from moisture and incompatible materials like strong bases and oxidizers. Protect from light and avoid exposure to air, as the compound is moisture-sensitive and may hydrolyze or release hazardous gases upon contact with water.
    Application of 4-Chloro-3-Sulfamoylbenzoyl Chloride

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

    We supply 4-Chloro-3-Sulfamoylbenzoyl Chloride as a high-purity intermediate for a limited range of specialized downstream chemical sectors. The following sections describe actual industrial use cases within regulated supply chains, focusing on compliance, composition, processing, and end product formation at plant scale.

    1. Pharmaceutical Sulfonamide Synthesis

    In active pharmaceutical ingredient production, our material serves as a key acylating intermediate for synthesizing sulfonamide antibiotics and antihypertensive APIs. Production sites formulate this compound into the molecular backbone through nucleophilic substitution steps to obtain specific benzoyl sulfonamide pharmacophores. Batch processing operators control reaction pH and temperature to prevent degradation of the sulfonyl chloride group; operators document control points for traceability and GMP audit.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • EU EudraLex Volume 4 guidelines for finished pharmaceuticals
    • USP and Ph. Eur. monograph requirements for sulfonamide APIs
    • FDA 21 CFR Part 211 – Current Good Manufacturing Practice

    Typical usage ratio

    • 0.98–1.05 molar equivalents per unit of amine nucleophile
    • The ratio adjusted based on the reactivity of co-reactants and desired yield (95%+ in most runs)

    Downstream process integration

    • Added in the early synthesis stage after amine protection steps
    • Dosed under nitrogen and low moisture conditions to prevent hydrolysis
    • Closely monitored for excess acid chloride removal by neutralization
    • Followed by crystallization and multi-stage purification before bulk API isolation

    Final product types

    • Sulfonamide antibiotic APIs for oral and injectable dosage forms
    • Antihypertensive agent intermediates
    • Bulk active pharmaceutical substance for further downstream compounding
    • Reference standards for pharmaceutical QC laboratories

    2. Advanced Agrochemical Formulations

    Our factory manufactures this compound for use as a reagent in selective synthesis of herbicide and fungicide active ingredients. Agrichemical formulators react it with heterocyclic amines to produce substitution products with specific aromatic sulfonyl functionalities for enhanced field stability and crop safety. The technical conversion occurs under closely validated protocols due to toxicological concerns for downstream handling and environmental fate.

    Industry compliance standards

    • FAO/WHO Joint Meeting on Pesticide Specifications (JMPS) standards
    • OECD GLP requirements for test material documentation
    • ISO 9001:2015 for quality management in agrochemical plants
    • EU Regulation (EC) No 1107/2009 for plant protection product actives

    Typical usage ratio

    • 0.90–1.03 molar equivalents based on targeted sulfonylation yield
    • Adjusted for batch scale and degree of substitution required by molecule design

    Downstream process integration

    • Introduced post pre-activation of aromatic systems
    • Metered addition ensures full conversion and reduces waste stream generation
    • Integrated in closed-system reactors with full containment
    • Followed by in-line neutralization and workup to prepare technical-grade actives

    Final product types

    • Sulfonylurea herbicide actives for cereals and rice crops
    • Fungicide intermediates destined for industrial seed treatment
    • Precursor for post-emergence weed control actives
    • Final package-ready technical agrochemical powders

    3. Specialty Dye and Pigment Manufacture

    Leading dye producers use this compound as an acylating and sulfonating building block in synthesizing specialty azo and anthraquinone dyes. Short-chain intermediates derived from it provide unique acid resistance and color fastness. Formulators track sulfonamide introduction to tightly control chromophore structure and meet textile sector wash durability standards. QC labs conduct batchwise IR/NMR analysis for residual chloride and purity before advancing to coupling.

    Industry compliance standards

    • OEKO-TEX® Standard 100 for textile dye inputs
    • REACH Regulation (EC) No 1907/2006 for chemical safety
    • GOTS (Global Organic Textile Standard) Approved Inputs policy
    • ISO 14001:2015 for environmental management systems in chemical production

    Typical usage ratio

    • 0.85–1.10 equivalents per primary aromatic amine or phenol
    • Loadings tuned for chromophore purity and depth of shade in final pigment

    Downstream process integration

    • Fed to sulfonation reactors during early-stage dye fragmentation
    • Processed under strict temperature and pH control for chromophore definition
    • By-products separated prior to final diazotization or coupling
    • Final pigments milled and standardized to textile manufacturer requirements

    Final product types

    • Acid-resistant textile dyes for wool and polyamide fiber
    • Colorfast high-performance pigment powders
    • Reactive dye intermediates for further finishing
    • Water-stable inkjet dye components

    4. Electronic Photoresist Material Production

    Producers of advanced PCB and microelectronics coatings source this material for the synthesis of negative and positive photoresist precursors. It forms stable benzoyl sulfonamide moieties within synthetic polymers, enhancing performance under UV exposure and etching chemical conditions. Manufacturing lines precisely meter addition in monomer block assembly, with downstream polymerization tailored to suit lithography process steps in high-density circuit fabrication. Analytical teams verify sulfonamide insertion using NMR and MS techniques to satisfy validation protocols.

    Industry compliance standards

    • IPC-6012: Qualification and Performance Specification for Rigid Printed Boards
    • IEC 60194-5: Printed Boards Design Standards
    • ISO 9001:2015 for advanced material manufacturing
    • RoHS Directive compliance for electronic input materials

    Typical usage ratio

    • 0.80–1.20 equivalents per target functional group in copolymer blend
    • Ratio varies by polymer architecture and target photo-patterning resolution

    Downstream process integration

    • Introduced during pre-polymer resin blending before final polymerization
    • Reacted within solution phase to minimize exposure to moisture and air
    • In-process quality sampling checks for incomplete incorporation
    • Final resin tailored for viscosity and application performance in photolithography

    Final product types

    • Photoresist coatings for semiconductor wafer fabrication
    • Advanced PCB imaging resins
    • UV-curable polymer blends for MEMS devices
    • Specialized etch-resistant films for multilayer circuits
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    Certification & Compliance
    More Introduction

    Introducing Our 4-Chloro-3-Sulfamoylbenzoyl Chloride: Precision and Performance Rooted in Chemistry

    At our manufacturing facility, the story behind 4-Chloro-3-Sulfamoylbenzoyl Chloride has grown out of decades of hands-on work with aromatic intermediates and fine chemicals. We don’t just ship containers with inventory codes on their side. We follow every kilo from raw material sourcing through to finished product, making sure our batches deliver on the demanding technical needs of modern synthesis, particularly for pharmaceuticals, agrochemicals, and advanced polymers.

    Purpose and Application: Built from the Ground Up for Serious Synthesis

    4-Chloro-3-Sulfamoylbenzoyl Chloride is not a bulk commodity. The strict structure of this compound—chlorine at the fourth position, the sulfamoyl group at the third, and benzoyl chloride at the core—gives it a unique profile that few other intermediates can substitute. Chemists rely on its dual reactivity: the acyl chloride function welcomes nucleophilic attack, while the sulfamoyl moiety serves as a versatile handle, especially for sulfonamide or urea formation.

    Over years of production, we see this product gravitate mainly into the development of sulfonamide antibiotics, high-value crop protection agents, and specialty dyes. Some R&D groups use it in exploring new coupling reactions, chasing performance targets that older benzoyl chlorides cannot reach. Others are interested in the precise modulation of electronic effects on the aromatic ring when they design new ligands or catalysts.

    Specifications: Not Just a Number, But a Commitment

    Our 4-Chloro-3-Sulfamoylbenzoyl Chloride comes under the model designation CSBC-98, representing our commitment to deliver a minimum assay of 98% by HPLC. From experience, dropping below this threshold introduces contamination in final formulations, especially in pharma routes. Each run is tested not only for purity, but also for residual solvents (commonly acetonitrile and dichloromethane), heavy metal content, water, and related benzoyl impurities.

    Solid white to off-white crystalline powder signals a successful batch. Free-flowing and low in moisture uptake, it handles well on lab benches and in process vessels. We keep particle size within an 80- to 200-mesh window—enough to avoid dust explosions and ensure rapid dissolution, without caking or compaction issues during storage or transfer.

    What Sets It Apart: Learning Through Practice

    In our own reactors, we’ve tested analogous compounds like 3-chlorobenzoyl chloride, 4-methyl-3-sulfamoylbenzoyl chloride, and 3,4-dichlorobenzoyl chloride. None deliver the same blend of selectivity and reactivity. Removing the sulfamoyl cuts down target binding in sulfonamide synthesis. Moving the chlorine or shifting groups around the aromatic ring changes solubility and sometimes kills yields in downstream acylations or amidations.

    We have also seen the results of poorly controlled batches from outside vendors: sticky powders with high water content, residual organics, or color contamination—none of which perform well in precision synthesis. Years of batch-to-batch consistency have taught us that attention to every synthesis and purification step makes or breaks reliability.

    Our Approach: From Raw Material Choice to Drum Filling

    Sourcing purified 4-chloro-3-nitrobenzoic acid and sulfamoyl chloride, we subject incoming lots to full analysis before tanking them. Our process skips shortcuts: oxidative chlorination under nitrogen, strict temperature control, and staged addition of reagents. Any hint of side reactions (overchlorination, over-sulfonation, or partial hydrolysis) triggers scrapping the charge.

    Hydrochloric acid release, water exclusion, and solvent recycling aren’t just compliance checkboxes for us. They represent a day-to-day reality; every kilogram of off-gas, every leaking flange, and every sample impurity trace back to manual steps and operator skill. Distillation under reduced pressure, filtration through inert beds, and rapid drying keep contamination low and color within spec.

    Final weighing, packaging, and labeling are coordinated by a tech team that understands how damaging a small bit of packaging resin or unnoticed fiber can be. Packed in moisture-barrier drums, with inert gas overlay, our product goes out ready for sensitive synthesis work, not left open to ambient humidity or bio-contaminants.

    Real-World Experience: Listening to Chemists and Engineers

    Customers at development and manufacturing sites give us hard feedback—not just on paper specifications, but on issues like unexpected reactivity, bottlenecks in solvent washes, or handling hazards. Over time, we tweaked crystal size distribution, optimized drying temperature, and improved stability under long-term storage not based on theoretical concerns, but because a contract manufacturer struggled with material breaking down after months on a warehouse shelf.

    Some teams care about heavy metal ppm levels more than HPLC area percent. Certain API routes flag secondary aromatic substitution. We keep our process flexible enough to adjust, either tightening specifications or splitting production lots. This willingness to adapt has saved downstream partners tens of thousands of dollars in troubleshooting costs, months of reruns, and, in some cases, entire product launches.

    For agrochemical users, we have received questions about how our intermediate interacts with specific protecting groups or solvents. We share real NMR and LC-MS data with partners and walk through side reaction risks, helping them design workups that avoid polymerization or catalyst poisoning.

    Handling, Storage, and Logistics: Owning Every Step

    Transporting a reactive acyl chloride demands reliability in moisture exclusion. Desiccated warehouse space, regular Karl Fischer titrations on outbound samples, and sealed drums are basic expectations. The reality includes temperature tracking, shock protection during shipping, and backup plans for customs delays. We’ve seen batches get held up under hot weather, and learned to test for thermal stability and cap any weak points that might let in air or water vapor.

    Clients have told us about issues with other suppliers where intermediates degrade into hydrochloric acid or hydrolysis products. Based on this, we precondition packaging, line all internal surfaces, and monitor headspace gas composition where necessary.

    Manufacturing Challenges: Not All Syntheses Are Created Equal

    Anyone who has run a scale-up knows that each raw material brings its own quirks. Some batches of 4-Chloro-3-Sulfamoylbenzoyl Chloride require closer monitoring to catch side chain impurities that come from variable supply chain quality upstream. We invested in multi-level filtration and in-line spectroscopy for real-time tracking.

    Temperature spikes during acyl chloride formation can throw off yield or generate byproducts. Our engineers spent months fine-tuning jacketed reactor profiles and optimizing agitation speeds until we hit our current reproducibility targets.

    Purification, another major challenge, draws on years of experience. The right solvent combination makes all the difference; cut corners with a cheaper solvent, and you accumulate impurities that haunt every downstream chromatogram. Through our own stumbles, we learned the value of closed-loop solvent analysis and tracked purity batches. As a result, our product ships with less than 0.5% total impurities, on average.

    Compliance and Traceability: Not Just Forms, but Real Accountability

    Auditors sometimes see our documentation on 4-Chloro-3-Sulfamoylbenzoyl Chloride and comment on the detail. We don’t treat this as box-checking—our own product stewardship depends on tracking each kilogram by lot, recording production technician, start and finish dates, all critical equipment readings, and in-process test results.

    We keep electronic logs and paper backups for all production cycles. This record-keeping isn’t glamorous, but when a downstream synthesis faces a problem, we can retrace every step to locate a root cause and recommend next steps.

    Environmental Responsibility: Beyond Minimum Compliance

    We have a vested interest in minimized waste output, solvent recovery, and safe byproduct control. The chloro- and sulfonyl intermediates present in our process streams require careful handling to avoid environmental and occupational risk. Regular air and water monitoring, closed ventilation, and rapid neutralization minimize exposure. Our investment in emissions scrubbers, distillate reclaim, and onsite solvent distillation started decades ago to reduce regulatory and reputational risk.

    We collaborate with specialty waste handlers for chlorinated streams and remain responsive to updated local environmental rules. Zero visible emissions has become the target; any deviation brings immediate process review and, if needed, shutdowns for system checks and repairs.

    Supporting R&D Collaboration

    Working directly with R&D teams, we help troubleshoot reactivity issues and can tailor properties when necessary—say, optimizing the residual moisture for catalysts sensitive to trace water or pre-granulating for high-speed auto-dosing lines. We lean on decades of hands-on work to recommend storage guidelines and blending practices that keep this intermediate stable and ready for use throughout research cycles.

    Feedback from universities and process development arms continually sharpens our production. Some researchers have needed highly sensitive material for NMR studies without common stabilizers; others have a periodic need for altered mesh size for reaction optimization. We learn alongside them, and in turn, future-proof our process for the next generation of discoveries.

    Safety in Handling: Transparency from Milligram to Metric Ton

    Safety is not theoretical for us. The acyl chloride group in 4-Chloro-3-Sulfamoylbenzoyl Chloride presents hazards: corrosivity, fuming in moist air, and possible skin and respiratory irritation. We advocate not just for safe shipment, but point out lab-specific risks drawn from our own experience—from unexpected exotherms on rapid addition, degraded gloves, to lingering fumes in small-scale workups.

    We walk partners through PPE options, ventilation, and real-world spill handling. On occasion, we've been called in to troubleshoot incidents, helping downstream teams source proper absorptive materials or evaluate on-site neutralization strategies. We recommend regular lab training, secondary containment for scale-up, and frequent checks on storage conditions based on our warehouse learnings.

    The Human Factor: Building Value through Knowledge

    Behind every packaged drum is an operator watching the pressure gauge, a QC chemist running titrations, and a scheduler juggling dozens of parallel syntheses. This hands-on involvement makes each shipment a personal investment. Our staff flag potential problems, recall historical quirks, and maintain continuity across production seasons.

    Mistakes have taught us as much as successes. Early on, we lost a portion of a batch to air ingress from a faulty valve. It cost us time and money, but the incident led to tighter inspection protocols and daily review meetings. The knowledge accumulated after years of making 4-Chloro-3-Sulfamoylbenzoyl Chloride now flows from senior technicians to newer hires, keeping quality high and troubleshooting nimble.

    Limitations and Emerging Solutions

    Even with experience and robust controls, certain challenges persist. Reagent fluctuations and shipping delays can slow production or increase costs. Sourcing ultra-pure starting materials sometimes faces regional or global scarcity. Our response involves dual sourcing and maintaining local partnerships with analytical labs for verification and recertification.

    Process intensification remains an ongoing pursuit. Continuous processing and inline purification tech are showing early promise for improving energy efficiency and further shrinking impurity profiles. We participate in industry consortia to stay ahead of regulatory change, formulating scenarios for rapid compliance transition when the need arises.

    Long-term, automation will gradually lessen the manual oversight required, but real expertise remains essential for judgment in troubleshooting cycles and interpreting nuanced analytical results. Pairing know-how with new tools keeps our output well above commodity benchmarks, even as markets and regulations evolve.

    Final Perspective: Why 4-Chloro-3-Sulfamoylbenzoyl Chloride Matters

    This intermediate has become a key enabler of novel bioactive compounds and high-value end products. Its unique substitution pattern, structural features, and careful production lend an edge not just in lab-scale synthesis, but in full-scale industrial routes where risk, cost, and time are all critical. Our ongoing commitment to learning, rigor, and adaptation has made 4-Chloro-3-Sulfamoylbenzoyl Chloride a dependable option for companies seeking more than a standard material order.

    We see each batch as both a culmination of past work and a stepping stone to future chemistry. The real value emerges when collaborative partnerships lead to new insights, faster troubleshooting, and the confidence that, from synthesis to shipment, every detail has been considered.