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2-Nitrobenzenesulfonyl Chloride

    • Product Name 2-Nitrobenzenesulfonyl Chloride
    • Alias Ns-Cl
    • Einecs 221-146-3
    • 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

    635183

    Chemical Name 2-Nitrobenzenesulfonyl Chloride
    Synonyms Ortho-Nitrobenzenesulfonyl chloride, o-Nitrobenzenesulfonyl chloride, 2-Nitrobenzene-1-sulfonyl chloride
    Cas Number 18110-15-7
    Molecular Formula C6H4ClNO4S
    Molecular Weight 221.62 g/mol
    Appearance Yellow to brown crystalline solid
    Melting Point 68-72°C
    Boiling Point Decomposes before boiling
    Solubility Slightly soluble in water; soluble in organic solvents like acetone and dichloromethane
    Density 1.65 g/cm³
    Purity Typically >98%
    Storage Conditions Store in a cool, dry place; keep container tightly closed; protect from moisture

    As an accredited 2-Nitrobenzenesulfonyl Chloride factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 2-Nitrobenzenesulfonyl Chloride, 25g: Supplied in a sealed, amber glass bottle with tamper-evident cap and hazard labeling for safe storage.
    Shipping 2-Nitrobenzenesulfonyl Chloride should be shipped in tightly sealed containers, away from moisture, heat, and incompatible substances. It must be packed in accordance with hazardous chemical shipping regulations, clearly labeled, and accompanied by appropriate safety documentation. Handle with care to prevent leaks or accidental exposure during transit.
    Storage 2-Nitrobenzenesulfonyl chloride should be stored in a tightly sealed container, away from moisture, heat, and direct sunlight. It should be kept in a cool, dry, and well-ventilated area, separate from incompatible substances such as strong bases, oxidizers, and water. Use appropriate secondary containment to prevent leaks and label storage clearly for hazardous and corrosive materials.
    Application of 2-Nitrobenzenesulfonyl Chloride

    Applications of 2-Nitrobenzenesulfonyl Chloride in Industrial Manufacturing

    As a direct manufacturer of 2-nitrobenzenesulfonyl chloride, we support a range of specialized chemical sectors. This compound functions as a key intermediate across multiple processing chains requiring high-purity, reliable supply, and tight process controls. Below, we outline primary industrial applications with relevant regulatory, formulation, and production details.

    1. Pharmaceutical Intermediate Synthesis

    Our 2-nitrobenzenesulfonyl chloride plays an essential role in synthesizing active pharmaceutical ingredients (APIs) and advanced intermediates. Reacting as a sulfonylating agent and protective group source, it aids in the selective functionalization of amines and alcohols. Its purity and low residual contaminants are critical, especially for small-molecule drug development such as angiotensin receptor antagonists and specialty antibiotics. Companies employ it in multi-step organic syntheses to introduce sulfonamide groups under tightly monitored parameters to ensure downstream GMP compliance and batch consistency.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice Guide (for API process steps)
    • European Pharmacopeia (Ph. Eur.) and United States Pharmacopeia (USP) monographs for intermediates
    • FDA 21 CFR Part 211 for finished drug product manufacturing
    • ISO 9001:2015 Quality Management Systems (raw material traceability)

    Typical usage ratio

    • Employ at 1 to 1.3 molar equivalents relative to primary amine substrates; adjusted based on side-reaction suppression and selectivity needs in API intermediate operations

    Downstream process integration

    • Charged during amidation or sulfonation stage, under inert atmosphere and temperature-controlled reactors; integrated before crystallization and API purification

    Final product types

    • Cardiovascular drug intermediates
    • Non-beta-lactam antibiotic precursors
    • Sulfonamide-based antimetabolite APIs
    • High-purity fine chemicals for regulated pharmaceutical production

    2. Protecting Group Chemistry in Peptide and Oligonucleotide Synthesis

    In peptide and nucleic acid synthesis, 2-nitrobenzenesulfonyl chloride serves as a selective protective group for amino and hydroxyl functionalities. CDMO and research labs use it to block reactive sites during solid-phase and solution-phase synthesis, preventing side reactions and enabling specific deprotection strategies in the sequence assembly. Its removal under mild reductive or nucleophilic conditions makes it valuable for complex sequence assembly, and process validation steps require strict impurity controls.

    Industry compliance standards

    • Organisation for Economic Co-operation and Development (OECD) GLP requirements (for reference standards)
    • USP general chapters <1043> for ancillary materials in oligonucleotide drug substance and product manufacturing
    • ISO 13485 for quality management in synthesized biomolecules used in diagnostics
    • REACH (EC) No 1907/2006 for chemical handling in R&D and production

    Typical usage ratio

    • Added at 1.05 to 1.2 equivalents relative to target amino group; adjusted according to resin loading density and length of the peptide or oligonucleotide

    Downstream process integration

    • Enters the solid-phase peptide or nucleic acid synthesis cycle at the protecting group installation step; removed by targeted deprotection after chain elongation

    Final product types

    • Therapeutic peptides
    • Antisense oligonucleotide APIs
    • Diagnostic synthetic oligos
    • Peptide-based research reagents

    3. Agrochemical Synthesis (Herbicide and Fungicide Intermediates)

    2-Nitrobenzenesulfonyl chloride acts as a sulfonylating agent in the production of sulfonylurea herbicides and certain fungicides. Leading agrochemical firms utilize it for constructing sulfonamide or sulfonylurea linkages via controlled, large-scale reactions. Its role in early-stage intermediate preparation ensures effective downstream coupling, ultimately supporting products that must meet strict residue and purity standards for registration and market access.

    Industry compliance standards

    • FAO/WHO specifications for agricultural pesticide manufacturing
    • ISO 9001:2015 and ISO 14001:2015 for environmental and quality management in agrochemical production
    • OECD guidelines for the testing of chemicals (GLP for field trial and registration samples)
    • REACH (EC) No 1907/2006 for substance registration and use in Europe

    Typical usage ratio

    • Typically 1:1 molar ratio with amine precursors in sulfonamide functionalization; precise ratio tailored per desired purity and yield constraints

    Downstream process integration

    • Reactant charged in the intermediate synthesis stage for pesticide actives, followed by work-up and conversion to finished agrochemical molecules

    Final product types

    • Sulfonylurea herbicide intermediates
    • Sulfonamide-based fungicide actives
    • Pre-emergent and post-emergent weed control products
    • Crop protection agent formulations

    4. Specialty Dye and Pigment Manufacturing

    In dye chemistry, 2-nitrobenzenesulfonyl chloride is a sulfonating intermediary introduced to create unique pigment and dye precursors. Leading colorant manufacturers use it to adjust hue, solubility, and fastness in azo and sulfur dye classes. It enables precise functionalization needed for textile and ink applications, with process controls implemented to support REACH registrations and effluent minimization target specifications.

    Industry compliance standards

    • REACH (EC) No 1907/2006 compliance for industrial dyes and pigments
    • ZDHC MRSL (Zero Discharge of Hazardous Chemicals) for textile chemicals
    • ISO 9001:2015 for consistent batch-to-batch quality
    • OEKO-TEX Standard 100 (for dyes used in textiles with human contact)

    Typical usage ratio

    • Uses range from 0.95–1.1 equivalents per moles of amine or hydroxyl substrate in pigment and dye precursor functionalization

    Downstream process integration

    • Added after diazotization or as part of coupling reactions during chromophore synthesis; followed by purification steps to minimize color impurities

    Final product types

    • Sulfonated azo dyes
    • Reactive dyes for cotton and cellulose fibers
    • Sulfur-based pigments
    • Colored inks for industrial and textile printing

    5. Photolithography and Photoresist Manufacture (Electronics Chemicals)

    Electronics manufacturers deploy 2-nitrobenzenesulfonyl chloride during photoresist formulation for semiconductor and printed circuit board fabrication. It introduces precise sulfonyl groups to enhance sensitivity and resolution in positive or negative photoresist resins. Process engineers incorporate this material into resin modification or monomer functionalization steps, requiring stringent metal impurity and moisture controls to avoid device defects in downstream applications.

    Industry compliance standards

    • SEMI C1 and SEMI C93 standards for photoresist raw materials
    • ISO 9001:2015 Quality Management in electronic chemicals
    • Restriction of Hazardous Substances Directive (RoHS 2011/65/EU) for electronics end-use
    • IECQ QC 080000 (electronic component hazardous substance process management)

    Typical usage ratio

    • Typically 2–8% by weight of total monomer or resin content, adjusted for target image resolution and sensitivity of the photoresist

    Downstream process integration

    • Blended during polymer resin modification before solvent casting or spin-coating for wafer and PCB coating applications

    Final product types

    • Positive and negative photoresist formulations
    • Microelectronic imaging resins
    • Photolithography patterning materials
    • Printed circuit board imaging resists

    6. Polymer and Cross-Linking Additive Manufacturing

    Manufacturers incorporate this material as a functional cross-linking agent or chain modifier in tailored polymer resins, particularly in specialty engineering plastics and performance coatings. It enables reactive site introduction for subsequent grafting or network structure formation, with careful metering essential to meet mechanical property and heat resistance targets.

    Industry compliance standards

    • ISO 9001:2015 for quality-controlled polymer manufacturing
    • REACH pre-registration and evaluation for polymer additives
    • ASTM D256 and ASTM D638 for mechanical property validation in final resins
    • EU Packaging and Packaging Waste Directive (94/62/EC) for polymer applications in packaging

    Typical usage ratio

    • Generally 0.5–5% by weight as cross-linker or functional additive, tuned by molecular weight and target cross-linking density in polymer matrices

    Downstream process integration

    • Incorporated during compounding or extrusion stages, prior to resin molding, casting, or curing, enabling further functionalization or cross-link network formation

    Final product types

    • Specialty thermoset and thermoplastic resins
    • Functional coatings with improved abrasion or chemical resistance
    • High-performance adhesive systems
    • Polymer blends for engineered parts and packaging
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    Certification & Compliance
    More Introduction

    2-Nitrobenzenesulfonyl Chloride: A Manufacturer’s Perspective on Precision Chemistry

    Our Experience Producing 2-Nitrobenzenesulfonyl Chloride

    For decades, we have focused on synthesizing specialty sulfonyl chlorides for the global chemical industry. Among these, 2-Nitrobenzenesulfonyl Chloride (NBSCl) stands out for its versatility in organic transformations. Over the years, our production teams have fine-tuned every step, from raw material sourcing to final crystallization, to meet the expectations of pharmaceutical researchers, polymer engineers, and laboratory chemists who rely on reproducibility and purity.

    Product Overview: Model, Specifications, Physical Profile

    Each batch of 2-Nitrobenzenesulfonyl Chloride leaves our facility as an off-white to light yellow crystalline powder. Typical specifications reflect the expertise that comes from years of continuous improvement: assay values usually exceed 98%, moisture content remains below 0.5%, and melting range consistently falls between 83-87°C, minimizing batch-to-batch variability. These parameters aren’t corporate slogans — they’re hard-won outcomes of controlled reaction temperatures, careful distillation, and precise drying conditions.

    As a compound, 2-Nitrobenzenesulfonyl Chloride features a nitro group at the ortho position of the aromatic ring, together with the reactive sulfonyl chloride functional group. This pairing determines its chemical behavior during coupling, sulfonation, and protection reactions. Formulators appreciate its moderate solubility in organic solvents such as dichloromethane, acetonitrile, and ethyl acetate, which speeds up dissolution and simplifies recovery, saving research organizations both time and solvent costs.

    Why This Material Matters—And Where It Fits

    In synthetic chemistry, protecting groups are more than handy tools; they directly impact the yield, purity, and feasibility of complex multi-step sequences. Sulfonyl chlorides generally serve as efficient reagents for introducing sulfonate groups onto alcohols, amines, and other nucleophiles. The unique placement of the nitro group in this molecule increases the electron-withdrawing effect, which enhances the reactivity of the sulfonyl chloride moiety. End-users regularly point out how this difference matters when they need clean reactions and easy deprotection.

    Our experience has shown that 2-Nitrobenzenesulfonyl Chloride outperforms its analogs, such as para-nitro- or unsubstituted benzenesulfonyl chlorides, in certain protection and activation chemistries. For example, researchers synthesizing biologically active peptides or oligonucleotides cite its reliability when protecting amino or hydroxy groups under mild conditions. After the key transformations are done, the nitro group allows deprotection under specific nucleophilic or reductive conditions, reducing the risk of side reactions that degrade product purity.

    Comparing to Other Sulfonyl Chlorides: Not All Are the Same

    Chemists familiar with benzenesulfonyl chlorides often ask why the ortho-nitro derivative deserves special attention. From firsthand manufacturing experience, side reactions often plague less activated chlorides, requiring harsher reaction conditions that can damage sensitive substrates. The ortho-nitro substituent on this product changes the electronic landscape, making it more reactive toward nucleophiles. Labs working on scale-up for new drug compounds report smoother processing and higher throughput with fewer purification steps when using our material.

    In contrast, standard benzenesulfonyl chloride or the para-nitro isomer do not deliver the same deprotection selectivity. Substitution at the ortho position creates a useful balance—reactive enough for efficient conversion, but not so forceful as to drive unwanted side chemistry or rapid hydrolysis when exposed to trace moisture. This chemical nuance is one reason why pharmaceutical and polymer companies return for our consistent batches, ensuring their own products don’t suffer unexpected losses during scale-up.

    Reliability from the Production Line: Why Consistency Is Critical

    No instrument or method replaces the value of consistent batch quality, especially when customers run high-stake processes that cost valuable time and resources. Every drum of our 2-Nitrobenzenesulfonyl Chloride reflects multiple quality checkpoints. Incoming aniline derivatives pass through several purification steps before nitration even begins. Electric heating mantles, precision thermocouples, and real-time monitoring keep reaction temperatures in a narrow band, preventing dark color byproducts that can arise during accidental overheating.

    After sulfonation, our vacuum filtration systems and proprietary washing protocols remove nearly all traces of inorganic salts and low-molecular-weight organics. Operators still remember challenges from early years when post-reaction drying sometimes left residual chlorides that promoted hydrolysis in customer’s labs. Those issues drove investments in new vacuum ovens and analytical methods. Now, even at kilogram scale, product moisture and acid chloride content remain reliably low.

    Product Use Cases: From Bench Research to Industrial Runs

    Bench chemists and process development engineers tend to notice the immediate benefits of using pure, freshly produced 2-Nitrobenzenesulfonyl Chloride. In medicinal chemistry, this compound acts as a go-to protecting group for amines, particularly during peptide synthesis where orthogonal strategies are needed. It helps chemists install stable sulfonamides, blocking undesired side reactivity during subsequent steps. Later, mild specific conditions release the protective group with minimal residue, often yielding a cleaner product than comparable sulfonyl chlorides.

    In materials science, this molecule functions as a key activator in polymer modification workflows. Surface functionalization of specialty resins, nanomaterials, or monomers benefits from the nitro group’s influence, allowing more precise grafting or crosslinking to boost end-use performance. Some industrial customers use it for selective activation of polyols or in the introduction of sulfonate esters with tailored performance, often with lower reaction temperatures and improved mass transfer — a direct advantage in scale-up.

    Handling, Storage, and Practical Concerns

    Sulfonyl chlorides require careful handling — not just for safety but to secure consistent performance. Our packaging comes lined with chemical-resistant polyethylene, heat-sealed after rigorous moisture analysis and nitrogen purging. Customers keep raw product under dry, cool conditions in tightly closed containers, out of direct light and away from sources of heat. Moisture ingress can cause hydrolysis, generating hydrochloric acid and reducing available active ingredient. We learned early on that minor packaging lapses could cause measurable declines in assay, so every shipment now includes batch moisture data and date of packaging for easy lab tracking.

    In the lab, standard operating procedures always include using dry glassware and anhydrous solvents. Whether end-users dissolve the material in dimethylformamide, chlorinated solvents, or simple ethyl acetate, they report that our product dissolves rapidly and produces minimal insoluble residue. We advise against using it directly in aqueous systems or with strong bases unless carefully neutralized, since unwanted hydrolysis leads to less predictable outcomes.

    Controlling Purity and Tracking Impurities: Beyond Routine Testing

    Clients performing sensitive syntheses often require extended impurity profiles, not just a basic certificate of analysis. Our methods go beyond basic titrimetric or HPLC checks: we screen for associated nitrobenzene, isomeric sulfonyl chlorides, and select volatile organic acids down to ppm levels. This extra vigilance pays off in downstream yields, a difference substantiated by feedback from pharmaceutical research teams and university collaborators.

    Our own in-process controls use a blend of gas chromatography, FTIR, and mass spectrometry. Rapid confirmation of molecular weight and structural integrity catches any off-spec batch before it reaches the mixing floor. Maintenance of trace-level purity isn’t guesswork — it requires deliberate investments in analytical equipment, regular calibration, and engineer training. Keeping these procedures tight avoids surprises at the customer’s bench, where even small inconsistencies can spell months of wasted effort in drug discovery or materials development programs.

    Innovation in Production: Meeting New Demands

    Chemistry doesn't stay static. As new reaction protocols emerge, clients often seek minor modifications in their orders — reduced particle size, higher color standards, or custom analytical documentation. Over the past five years, we’ve integrated additional recrystallization and milling steps, responding to requests for powders that disperse more rapidly and mix cleanly even at process scale. Some startups in next-generation electronics now specify micronized NBSCl for coating and specialty polymer work, prompting us to install new jet mills for dry sizing.

    Feedback loops run both ways. We routinely collaborate with R&D teams to troubleshoot unusual performance issues, starting from basic observations. Are there traces of catalytic poisons during metal-catalyzed couplings? Are unconverted anilines or sulfonic acids affecting downstream purification? Our manufacturing teams meet with application chemists to adjust drying and washing steps when new analytical methods highlight batch-to-batch micro-variations. These partnerships ground our production choices in actual laboratory realities, rather than theory.

    Sustainability and Regulatory Compliance

    Every specialty chemical facility faces scrutiny — both from local environmental agencies and from customers watching raw material choices. Our plant has moved toward greener production cycles by reclaiming spent acids, using closed-loop nitration reactors, and managing effluent with on-site treatment rather than shipping waste offsite. These decisions stem from years of keeping one eye on regulatory changes and another on cost control. We use only industrial grades of solvents and keep detailed documentation for batch origin, tracking every input for traceability.

    Our compliance group keeps product movement transparent through material safety data sheets and lot-level documentation. Chemists in regulated products — APIs and intermediates — expect exacting traceability, and pharmaceutical project leaders increasingly audit our site to ensure these requirements are met. We support registrations for international transport and supply, helping customers fulfill customs, safety, and environmental obligations with ease.

    Response to Market Trends: Quality Under Pressure

    In recent years, the shifting supply-chain landscape and increased demand for quality-controlled chemical inputs have sharpened focus within our team. Episodes of supply disruption for certain sulfonamide intermediates have underscored the importance of robust local manufacturing and flexibility in sourcing raw materials. We monitor shifts in upstream pricing for key inputs such as chlorosulfonic acid and ortho-nitroaniline, watching for signals that might affect downstream cost and lead times. When global freight tightens, our logistics crew coordinates shipments to reduce the risk of exposure to temperature or humidity changes in transit.

    Customers performing multi-ton syntheses appreciate that each kilogram reflects the same process diligence as smaller R&D lots. Past months have shown a rising trend toward in-house quality testing on receipt, with clients running NMR, LC-MS, and DSC on incoming batches. These practices highlight the trust—but also the responsibility—we carry as an original manufacturer, where overlooked impurities or subtle quality changes can cascade through a supply chain, affecting launches and regulatory submissions.

    What Sets Our 2-Nitrobenzenesulfonyl Chloride Apart

    Manufacturing isn’t just about assembling known recipes. Over years of feedback, adjustments, and continuous improvement, we’ve learned what makes a difference between usable chemical intermediates and truly reliable product. Clean starting materials, rare downtime for plant maintenance, and an emphasis on documentation give our production repeatability. Our staff often field calls from returning customers seeking reassurance about purity, delivery timelines, or suitability for new chemistry. We deliver not by promise alone, but through batches that pass on their own merits under customer scrutiny.

    For those exploring alternatives, we welcome bench trials and comparative analyses. Direct feedback from actual use helps us refine future production, and our technical support stands fully prepared to troubleshoot applications or adapt material according to emerging practices. This open dialogue, grounded in real-world chemistry, reinforces our belief that the value of a reagent isn’t captured in generic catalogs or distributor brochures but in lasting partnerships with scientists who rely on accuracy.

    Supporting Innovation—Staying Ready for Tomorrow

    As synthetic protocols grow ever more sophisticated, the drive for purity, reliability, and transparency only intensifies. Our ongoing response draws from decades of hands-on manufacturing, not only in the context of proven technology but with a view toward next-generation applications. Every new research field — whether in advanced catalysts, specialty polymers, or bioactive molecules — challenges us to raise production standards, expand analytical testing, and rethink old assumptions.

    We take pride in the journey each lot of 2-Nitrobenzenesulfonyl Chloride undertakes from our plant to our customers, knowing its ultimate worth is measured by the discoveries and products it enables. Through direct engagement, continuous learning, and a commitment to consistent quality, we’ll keep supporting chemists, engineers, and innovators who demand more from their chemical partners, today and in the future.