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2-Iodobenzene-1-Sulfonyl Chloride

    • Product Name 2-Iodobenzene-1-Sulfonyl Chloride
    • Alias IBS
    • Einecs 226-987-6
    • 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

    754304

    Product Name 2-Iodobenzene-1-Sulfonyl Chloride
    Cas Number 4457-34-1
    Molecular Formula C6H4IOSCl
    Molecular Weight 282.52 g/mol
    Appearance White to pale yellow solid
    Melting Point 111-115 °C
    Boiling Point Decomposes before boiling
    Solubility Soluble in organic solvents such as dichloromethane and chloroform
    Density 2.12 g/cm³ (estimated)
    Purity Typically ≥ 98%
    Synonyms 2-Iodophenylsulfonyl chloride
    Storage Conditions Store in a cool, dry place; keep container tightly closed
    Chemical Structure IC6H4SO2Cl
    Ec Number 224-639-3

    As an accredited 2-Iodobenzene-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 25g 2-Iodobenzene-1-sulfonyl chloride is provided in a tightly sealed amber glass bottle with clear hazard labeling.
    Shipping 2-Iodobenzene-1-sulfonyl chloride is shipped in tightly sealed containers, protected from light, moisture, and incompatible materials. Transport complies with local and international regulations for hazardous chemicals. Proper labeling and documentation ensure safe handling. It is typically shipped as a Class 8 corrosive substance, requiring careful handling and storage during transit.
    Storage 2-Iodobenzene-1-sulfonyl chloride should be stored in a tightly sealed container under an inert atmosphere, in a cool, dry, and well-ventilated area. Protect from moisture, heat, and direct sunlight. Store separately from incompatible substances such as strong bases, strong oxidizers, and water. Use appropriate secondary containment and clearly label containers to prevent accidental exposure or reactions.
    Application of 2-Iodobenzene-1-Sulfonyl Chloride

    Applications of 2-Iodobenzene-1-Sulfonyl Chloride in Industrial Manufacturing

    2-Iodobenzene-1-sulfonyl chloride supports specialized synthesis pathways across select industrial sectors. As a halogenated sulfonylating agent, manufacturers in pharmaceutical, agrochemical, functional materials, and specialty intermediates industries rely on its unique reactivity to enable downstream transformation steps that demand precise functionality and high consistency. Below we detail its main application segments, focusing on industrial compliance, rationalized addition rates, processing integration points, and commercial end products.

    1. Pharmaceutical Intermediate Synthesis

    Medicinal chemistry researchers and API plants use 2-iodobenzene-1-sulfonyl chloride as a key building block in the construction of N-sulfonylated heterocycles and halogenated scaffolds. It creates challenging arylsulfonamide motifs required in kinase inhibitors, antiviral agents, and cancer therapy intermediates. The compound's electrophilicity consistently delivers high conversions under controlled batch conditions, supporting scale-up to kilo and multi-kilo synthesis for advanced intermediates.

    Industry compliance standards

    • ICH Q7 GMP for Active Pharmaceutical Ingredients
    • USP/NF pharmacopoeial specifications for intermediates
    • EU GMP regulations Part II (API manufacturing)

    Typical usage ratio

    • 0.8–1.1 molar equivalents versus core amines or heterocycles; laboratories adjust based on substrate nucleophilicity and desired selectivity

    Downstream process integration

    • Charged directly into sulfonamidation or halogen coupling step in validated glass-lined reactors under nitrogen; followed by aqueous quench, phase separation, and purification

    Final product types

    • Small-molecule kinase inhibitors (e.g., N-sulfonylpyrimidines)
    • Anti-infective sulfonamides
    • Advanced halogenated intermediates for custom synthesis

    2. Agrochemical Intermediate Manufacturing

    Crop protection chemical companies employ 2-iodobenzene-1-sulfonyl chloride to introduce sulfonyl and halogen features into precursor molecules required for insecticides and fungicides. The reactivity profile supports the preparation of tailored sulfonamide linkers and aromatic iodides at precise integration steps, necessary for downstream cross-coupling or heterocycle formation in the active ingredient synthesis chain.

    Industry compliance standards

    • FAO/WHO Technical Specifications for pesticides
    • ISO 9001:2015 certified quality assurance for crop protection ingredients
    • REACH registration for intermediate handling

    Typical usage ratio

    • 0.95–1.05 molar equivalents as a limiting reagent, adjusted to minimize residual halide and maximize conversion per batch quality protocols

    Downstream process integration

    • Added during late-stage precursor modification in sulfonamidation or iodination prior to final cyclization or coupling

    Final product types

    • Sulfonylurea herbicide intermediates
    • Halogenated benzene-based fungicides
    • Pesticide active ingredient pre-cursors

    3. Chemical Research – Sulfonylase Inhibitor Library Generation

    Industrial-scale R&D and custom synthesis labs exploit this reagent’s sulfonyl chloride group for rapid parallel generation of aryl sulfonylated libraries targeting enzyme inhibition, notably sulfonylase and related targets. Effective in high-throughput array synthesis, the compound enables gram to multi-gram scale preparation for biological screening while supporting downstream purification and structural diversification.

    Industry compliance standards

    • ISO 17025 laboratory operations
    • OECD GLP guidelines for chemical handling
    • Company-level chemical library tracking and documentation per GxP

    Typical usage ratio

    • 0.9–1.2 equivalents per scaffold; researchers determine the ratio based on assay throughput and purity requirements of derivatives

    Downstream process integration

    • Introduced as a reagent in automation-compatible reactors; subsequent work-up typically involves solid-phase extraction or HPLC purification prior to assay or scale-up

    Final product types

    • Enzyme inhibitor screening libraries
    • Biologically active sulfonamides for target validation
    • Reference standards for analytical chemistry

    4. Electronic Material Functionalization

    Materials manufacturers utilize 2-iodobenzene-1-sulfonyl chloride to introduce tightly controlled sulfonyl and halogen groups into aromatic backbones of advanced functional materials for applications in organic electronics, lithium battery electrolytes, and specialty sensors. It forms tailored intermediates for further coupling and polymerization, ensuring strict batch-to-batch consistency required in high-performance electronic grade products.

    Industry compliance standards

    • ISO 9001:2015 certified QMS for advanced materials
    • RoHS Directive compliance for restricted substances
    • IEC 62474 material declaration and documentation

    Typical usage ratio

    • 0.7–1.0 molar equivalents relative to target aromatic units; variation depends on polymer chain length control and desired substitution pattern

    Downstream process integration

    • Employed in key functionalization stages prior to polymerization or grafting, with subsequent thermal or catalytic coupling steps under inert atmospheres

    Final product types

    • Organic semiconductors for thin-film transistors
    • Functionalized monomers for battery separators
    • Specialty sensing layers for analytical devices

    5. Specialty Dye and Pigment Intermediate Production

    Producers of specialty dyes apply 2-iodobenzene-1-sulfonyl chloride to introduce tailored sulfonyl and halogen patterns on aromatic chromophores, tuning solubility and absorption properties for high-purity colorant production. The compound enters controlled synthesis steps to prepare charge-transfer dyes, photographic sensitisers, and pigments for demanding optical and imaging applications.

    Industry compliance standards

    • ETAD (Ecological and Toxicological Association of Dyes and Organic Pigments Manufacturers) guidelines
    • ISO 9001:2015 for pigment and dye manufacturing
    • REACH registration for specialty chemical intermediates

    Typical usage ratio

    • 1.0–1.3 equivalents per dye precursor, optimized based on chromophore functionality and targeted yield requirements

    Downstream process integration

    • Reacted during aryl sulfonation and halogenation stages before final azo coupling or condensation; process includes thorough washing and filtration to meet optical purity standards

    Final product types

    • High-performance organic pigments for printing
    • Charge-transfer dyes for OLED and photovoltaic devices
    • Sensitizer dyes for photographic films
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    Certification & Compliance
    More Introduction

    2-Iodobenzene-1-Sulfonyl Chloride: Behind the Reactivity

    Practical Manufacturing Experience with a Unique Sulfonyl Halide

    In the modern landscape of aryl sulfonyl chlorides, 2-iodobenzene-1-sulfonyl chloride carries a reputation that often draws the attention of process chemists and medicinal research labs. As a producer immersed in daily operations, I’ve seen this compound come off the reactor and head out into applications where lesser reagents fall short. From batch homogeneity to handling, its properties regularly surprise even experienced teams.

    Identity and Consistency

    This molecule—known among researchers for its precision reactivity—comes straight from a clear coupling of iodination and chlorination steps. We run strict controls on every batch. Color retention and moisture content speak volumes to customers long before any paperwork or COA reaches them. Conversion efficiency never tells the whole story; we rely on careful in-process checks, from crystallization temperature to the tactile feel during isolation. It’s not hard to spot the batches that ran too warm or picked up humidity, so we’ve set our own boundaries for when to rework a charge.

    Specifications Matter: Purity, Appearance, and Handling

    The model we offer, under the chemical formula C6H4ISO2Cl, weighs in with a molar mass near 302.53 g/mol. Specifications focus on purity—over 98% by HPLC—since impurities like unreacted sulfonic acid or oxidative byproducts can shut down a reaction in scale-up. In the warehouse, skilled workers can spot a subpar drum by its off-white cast or sticky consistency. Packing always happens under dry nitrogen, minimizing hydrolysis. Many shops learn the hard way how fast sulfonyl chlorides can pick up water, but a well-sealed vessel makes the difference between a steady hand addition to a flask and a fizzing, wasteful mess.

    Why Use 2-Iodobenzene-1-Sulfonyl Chloride?

    This reagent brings more than commodity functionality. In coupling and functional group interconversion, particularly in modern cross-coupling, it stands apart by where it places its reactivity—on the iodine and the sulfonyl chloride. Complex molecule synthesis, such as in pharmaceutical intermediates or agrochemical discovery, leverages these orthogonal handles. It offers routes not easily accessed by other sulfonyl chlorides.

    Palladium-catalyzed couplings benefit from iodine, which leaves more readily during oxidative addition than bromine or chlorine. This translates into better yields and fewer side products. In sulfonamide bond formation, the chloride leaves cleanly, anchoring the sulfonyl group onto amines and opening the field for diversity-oriented synthesis.

    Process Realities: Safety, Storage, and Worker Experience

    Everyone working in a chemical plant knows sulfonyl chlorides have a sharpness in the air when unchecked. 2-iodobenzene-1-sulfonyl chloride is no exception. No process engineer wants to track chlorides through vents or deal with a spill of sticky, lachrymatory material. Routine means controlling ambient humidity and keeping up with prompt cleaning. In practice, our facility maintains a dry zone wherever this product is packed or transferred.

    Drums and bottles run out with desiccant packs before heading further downstream. Not only does this ensure batch integrity, it prevents clotting and sticky build-up that can slow down production lines in customer facilities. Experience on our packing lines shows us: even small lapses in container sealing or excess exposure during changeover bring costly delays and rework. We run a tight ship to keep reactivity high and off-odors out.

    Comparisons and Contrasts with Other Sulfonyl Chlorides

    Our shops have handled a wide catalog of sulfonyl chlorides: from the basic benzenesulfonyl chloride to complex fluorinated versions. Each reacts differently with the air, amines, or alcohols. What sets 2-iodobenzene-1-sulfonyl chloride apart is its dual functionality. Compounds with only alkyl or phenyl substitutions rarely bring this level of selective application in cross-coupling processes.

    Direct comparison highlights a difference beyond price. Benzenesulfonyl chloride, for example, offers solid sulfonamide formation but lacks the leaving group flexibility. The iodine atom in our compound acts as a switch for metal-catalyzed chemistry, providing access to Suzuki, Sonogashira, and related couplings not easily achieved with non-iodinated sulfonyl chlorides. From a manufacturing lens, we notice the increased sensitivity during synthesis, thanks to the heavy atom and electron-rich aromatic system. It means tighter monitoring and smaller allowable windows on process parameters.

    Some customers come in thinking a standard sulfonyl chloride can substitute in their route. Delays and low conversion rates quickly change that impression. We’ve spent years tracking these stories; they tend to end with a returned drum and an urgent call for our product. Our own development teams rely on similar differences to push through bottlenecks in new process routes or to replace hazardous alternatives.

    Quality from Supply Chain to End-User Lab

    Maintaining supply integrity starts from raw iodine and high-grade sulfur chlorides. Every failed batch leaves a log, not a landfill. We clean reactors with solvent flushes, monitor filtration residues, and don’t shy away from recalibrating glassware or troubleshooting stray discoloration in the filter cake. If a batch looks questionable, it’s held back until we can pinpoint and resolve the issue. This improves trust on both ends; we send out only what meets internal standards.

    Downstream, our partners in drug development and materials chemistry draw sharp lines on impurity profiles. They file analytical requests that sometimes push us to re-examine crystallization conditions or to screen new purification media. Every specification update is the product of both sides’ experience—their pain points in scaling up, our ability to adjust upstream processing, and a shared goal to minimize surprises mid-synthesis.

    As regulation tightens and synthetic targets become more challenging, transparency and end-to-end documentation bear more weight. We keep detailed batch records and reactivity test data available, sometimes tracing an impurity ghost back several months or batches. Such vigilance means fewer project halts for our clients—fewer surprises in the HPLC readouts, less powder lost to uncertain purity, and more confidence running their next reaction.

    Applications: Real-World Use Cases

    Pharmaceutical companies tap into 2-iodobenzene-1-sulfonyl chloride when building out new core scaffolds. One well-known use ties to its role as a precursor in C-S bond formation and in selective derivatization of heterocycles. The coupling versatility intrinsic to the aryl iodide moiety allows medicinal chemists to build complicated libraries by simple amine or arylation reactions. Over the years, feedback from R&D centers points to shorter development cycles and increased confidence using our material, highlighting the savings in both time and solvent volume.

    In materials science, researchers apply it for introducing sulfonyl functionalities onto polymer backbones or in the assembly of light-absorbing groups in optoelectronic devices. Here, the combination of sulfonyl chloride and iodine not only facilitates efficient post-modification chemistry but also enables further transformations impossible with less reactive groups. Even in failure stories—batch losses from humidity ingress during scale-up or complications from equipment fouling—a clear record and consultation with our teams have enabled customers to recover from setbacks and tweak their protocols for future runs.

    Safety, Training, and Waste Management Observations

    A compound as reactive as this can’t be treated carelessly. All the experienced plant managers drill teams on the symptoms of exposure: burning eyes, persistent throat irritation, strange white crusts on fittings. We stay alert to bulk tank monitoring, and our senior technicians regularly update the drums’ material safety instructions. Not every operation faces the same scale of risk, but scaling up always pulls unseen hazards into view. Leaks in standard couplings call for immediate isolation; if a drum tips over, clean-up suits and absorbent pads see use before a restart.

    Disposal practices adapt to new waste streams created by contaminated wrappers, wipes, or broken seals. Condensing off-gas, capturing acidic vapors, and neutralizing onsite reflect our ongoing work with regulators and third-party auditors. Even here, we’ve learned from past mistakes—poor ventilation or complacent assumptions about runoff have forced improvements in air handling and drum tracking. By matching procedures to the realities of high-volume manufacture, we create safer environments for staff and more reliable outcomes for end users.

    Challenges in Scale, Transportation, and Customer Support

    Demand rarely comes evenly; some seasons bring triple the normal orders. At full pace, reactors run hotter and tighter shift transitions pose more risk for cross-contamination. The logistics team tracks routes rigidly because winter cold or summer humidity will do their best to attack a well-packed drum. Containers travel with clear labeling, reinforced stoppers, and tamper-evident seals, based not on theoretical policy but the mishaps of real shipments over the years.

    We’ve fielded our share of urgent calls: a truck delayed by customs, a broken seal discovered two cities out, a batch stalling at the mixing tank because the powder fused overnight in a half-sealed bag. These are resolved less by script and more by experience, coordination, and knowing which step kept the last load pristine. The chain of custody doesn’t just ensure regulatory compliance; it feeds back into operational tweaks—shorter hold times, faster transit, or climate-controlled trucks.

    Support doesn’t end with delivery. Technical service specialists follow up, answer practical handling queries, or flag a suspicious off-odor. We build relationships that revisit not only past shipments but also future requirements, suggesting shifts in scale or even alternate pack sizes. This continuous cycle—problem, solution, feedback—keeps our processes aligned with every evolution in our clients’ chemistry.

    Future Outlook: Innovations and Regulatory Adaptations

    Chemical manufacturing evolves fast, and 2-iodobenzene-1-sulfonyl chloride rides that curve. Upcoming sustainable processes—from energy-minimized reactors to low-emission vent stacks—guide our investments and employee training. Regulatory agencies push for ever-tighter profiles in hazardous material tracking, and adapting to these requirements takes constant vigilance. We balance productivity and compliance not by shortcuts but by retooling: in updated containment, automating sampling, and upskilling both operators and management.

    On the product side, new synthesis routes seek to lower waste and reduce reliance on harsh reagents. Process chemists work on alternative chlorinating systems, minimizing gas evolution while heightening selectivity. Continuous reaction monitoring promises faster course-corrections, especially when a synthesis step threatens to spiral out with variable feed quality.

    End users benefit by receiving material with not just the right specifications but a cleaner lifecycle. Fewer process bottlenecks, improved shelf life, and fewer surprises under the microscope push research agendas forward. Our role as manufacturer means direct engagement; we don’t stand behind anonymous invoices or generic dispatch desks but respond to each customer milestone with adjustments born from production realities.

    Addressing Customer Concerns: Purity, Documentation, and Traceability

    Analytical chemists and process engineers alike press for documentation. Typical requests include NMR spectra, high-resolution mass spec traces, in-depth impurity breakdowns, and even images of isolated crystalline lots. Our labs run these as part of final batch release; if anything stands out—even a discrepancy in peak shape—discussion starts immediately between plant chemists and analysts. Tracking lot histories helps customers avoid costly mismatches in process runs and backs up troubleshooting when an unusual result emerges.

    Traceability extends from raw material procurement through final shipment. We reject speculation while preparing supplementary analysis, making use of up-to-date analytical methods. Should a batch fail to meet the predefined standards, our corrective actions unfold within days, not weeks. We avoid the cycle of returns and reworks through direct, experience-driven communication between operations and commercial teams.

    These lessons come from years of managing real supply chains—understanding what data matters most at the bench, which records unlock regulatory access, and which steps support patient safety and environmental integrity. In this way, we see every successful shipment as proof of applied knowledge, not simply a ticked box on a list.

    End User Collaboration: Feedback Loops and Shared Improvement

    Collaboration doesn’t always start at the drawing board, but almost every innovation or process improvement has roots in a problem flagged downstream: a reaction unexpectedly stalling, a viscosity spike in a tank, or an unreported off-gassing event. Our open-door habit means teams on both sides study these incidents and often design permanent fixes. Whether adapting new sampling gear, tightening shipment windows, or building multi-level containment, the improvements are shared—raising both customer confidence and plant efficiency.

    This hands-on, detail-focused approach sets the foundation for longer partnerships. Repeat customers aren’t won by advertising, but by proven results when pressure is high: a costly run at stake, a timeline under threat, cross-functional demands on documenation, or the simple ask for advice in prepping their next campaign. Plant experience here values practicality over promises—each shipment a handshake and a record to stand on.

    Closing Perspectives

    In the hands of practitioners, 2-iodobenzene-1-sulfonyl chloride does more than fill a space on a compound sheet. Every batch reflects the expertise gained from hands-on synthesis, vigilant quality control, transparent documentation, and a readiness to solve customer challenges on their own timelines. By consistently meeting fine-tuned specifications and adapting to rapid change, we reinforce not only the value of the product but the trust that every customer—and every lab bench—relies on.

    As regulatory oversight intensifies and applications branch further into specialty and life science sectors, the role of specialized manufacturers deepens. We keep our focus on the critical points in handling, purity, supply continuity, and accountability that shape not only production but also the very progress of the industries we serve.