Products

2-Nitrobenzenesulfonyl Chloride

    • Product Name: 2-Nitrobenzenesulfonyl Chloride
    • Alias: NsCl
    • Einecs: 221-984-3
    • Mininmum Order: 1 g
    • Factroy Site: Yudu County, Ganzhou, Jiangxi, China
    • Price Inquiry: admin@ascent-chem.com
    • Manufacturer: Ascent Petrochem Holdings Co., Limited
    • CONTACT NOW
    Specifications

    HS Code

    409261

    Chemicalname 2-Nitrobenzenesulfonyl Chloride
    Synonyms o-Nitrobenzenesulfonyl chloride
    Casnumber 612-24-8
    Molecularformula C6H4ClNO4S
    Molecularweight 221.62 g/mol
    Appearance Light yellow to yellow crystalline powder
    Meltingpoint 66-69°C
    Boilingpoint 241°C (decomposes)
    Solubility Insoluble in water, soluble in organic solvents like dichloromethane
    Density 1.60 g/cm³
    Purity Typically ≥98%
    Flashpoint 103°C
    Storageconditions Store in a cool, dry place, protect from moisture
    Smiles C1=CC=C(C(=C1)[N+](=O)[O-])S(=O)(=O)Cl

    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 Amber glass bottle containing 100 grams of 2-Nitrobenzenesulfonyl Chloride, labeled with hazard symbols and safety information.
    Shipping 2-Nitrobenzenesulfonyl Chloride is shipped in tightly sealed, corrosion-resistant containers, protected from moisture and direct sunlight. It should be handled as a hazardous material, following appropriate regulations for toxic and irritant substances. Ensure proper labeling and documentation, and transport in compliance with local, national, and international chemical shipping regulations.
    Storage 2-Nitrobenzenesulfonyl chloride should be stored in a tightly sealed container, in a cool, dry, well-ventilated area away from moisture, heat, and direct sunlight. Keep it separate from strong bases, alcohols, amines, and other incompatible substances. Use appropriate chemical storage cabinets and ensure containers are clearly labeled. Handle in compliance with relevant safety regulations to prevent exposure and degradation.
    Application of 2-Nitrobenzenesulfonyl Chloride

    Applications of 2-Nitrobenzenesulfonyl Chloride in Industrial Manufacturing

    As an established manufacturer of 2-Nitrobenzenesulfonyl Chloride, we have supported global chemical industries with this reagent in specialized downstream sectors for over a decade. Below, you will find detailed application cases reflecting exact integration points, industry regulatory needs, and technical handling practices from actual industrial customers. All listed scenarios reflect established and validated use cases in commercial manufacturing environments.

    1. Pharmaceutical Intermediate Synthesis: Amino Protecting Reagent

    Pharmaceutical API factories routinely employ 2-Nitrobenzenesulfonyl Chloride as a selective sulfonylating agent for the protection of primary and secondary amine groups during multi-step organic synthesis. The reagent enables chemists to isolate, purify, and further functionalize complex molecular structures in cephalosporin and penicillin derivative processes, where protection/deprotection cycling is mandatory for yield and purity.

    Industry compliance standards

    • ICH Q7 GMP for Active Pharmaceutical Ingredients
    • USP General Chapter <1078> Good Manufacturing Practices
    • European Pharmacopoeia (Ph. Eur.) monograph references for intermediate handling
    • FDA 21 CFR Part 211 (cGMP for Finished Pharmaceuticals, relevant for intermediate traceability)

    Typical usage ratio

    • 1.05–1.25 equivalents per mol of target amine group; precise dosing calculated according to substrate molecular weight, amination scale, and target selectivity. Deviations account for substrate impurity and process yield requirements.

    Downstream process integration

    • Material dosed at the dedicated sulfonylation step, typically after initial amination and base neutralization, and quenched/hydrolyzed during deprotection before final product crystallization.

    Final product types

    • Cephalosporin antibiotic intermediates
    • Piperazine derivative APIs
    • Sulfonamide antibiotics
    • Complex protected peptide intermediates

    2. Synthesis of Fluorescent Probes and Chemical Sensors

    R&D and production plants in the life science sector utilize the sulfonyl chloride group for covalent labeling of fluorophores and chemosensors. 2-Nitrobenzenesulfonyl groups provide unique electron-withdrawing properties, yielding high-sensitivity fluorogenic substrates commonly used in biological assays, cell imaging, and bioconjugation kits. Manufacturing quality and batch traceability remain crucial, due to the sensitivity needed in analytical detection products.

    Industry compliance standards

    • ISO 9001 Quality Management Systems (for analytical reagent production)
    • REACH Registration (EU) for chemical supply
    • OECD GLP Principles (for testing lab supply chains)
    • TUV or SGS purity verification if intended for regulated research markets

    Typical usage ratio

    • 0.8–1.2 equivalents relative to probe core molecule; slight excess optimizes reaction completion and minimizes unreacted labeling site loss. Adjustment made for desired substitution degree in multi-label syntheses.

    Downstream process integration

    • Introduced during late-stage condensation or aromatic substitution phase; reaction monitored by HPLC/LC-MS, followed by flash chromatography for probe isolation.

    Final product types

    • Turn-on/off fluorescent reagents for cell assays
    • Chemical sensor dyes for environmental monitoring
    • Bioconjugation kits for protein tagging
    • Diagnostic reporter molecule kits

    3. Agrochemical Intermediate Manufacturing

    Producers of crop protection chemicals and specialty agrochemical intermediates specify our material for selective sulfonylation steps in the development of herbicides and fungicide scaffolds. The electron-withdrawing nitro group greatly aids in ring activation, which is crucial for downstream modifications in heterocycle systems present in pesticide molecules. Regulatory-driven tracking and tight impurity control are standard for crop chemistry applications.

    Industry compliance standards

    • ISO 9001, ISO 14001 (environmental controls for agrochemical processes)
    • FAO/WHO Specification for Pesticide Intermediates
    • China GB 2763 (Maximum Residue Limits for Pesticides in Food)
    • Regulation (EC) No 1107/2009 (EU plant protection products)

    Typical usage ratio

    • 0.7–1.3 moles per mole of active moiety; ratio depends on specific step (monosubstitution preferred) and crop chemistry registration dossier requirements for by-product minimization.

    Downstream process integration

    • Used in intermediate functionalization stage before cyclization or halogenation; typically added in anhydrous DMF or DCM reactors under controlled temperature, followed by aqueous workup and extraction.

    Final product types

    • Triazole fungicide intermediates
    • Pyridine-sulfonyl herbicide precursors
    • Benzothiazole pesticide scaffolds
    • Sulfonyl urea preproducts

    4. Dye and Pigment Intermediate Synthesis

    Specialty dye and pigment manufacturers use 2-Nitrobenzenesulfonyl Chloride to introduce sulfonate groups onto aromatic rings, creating dyes with improved water solubility, acidity range, and reactivity towards fiber or surface coupling. Controlled sulfonylation also enables fine-tuning of absorption spectra, which directly impacts shade and color fastness qualities required for industrial textile, leather, and ink applications.

    Industry compliance standards

    • Oeko-Tex Standard 100 (for textile chemicals)
    • ISO 9001:2015 Quality Systems for dye manufacturing
    • ZDHC MRSL (Zero Discharge of Hazardous Chemicals)
    • EN 71-3 (dye safety for textiles and toys in the EU market)

    Typical usage ratio

    • 0.9–1.4 mole equivalents per aromatic substrate; preference varies by target shade intensity and degree of sulfonation, accounting for molecular weight differences and desired stage of sulfonyl group introduction.

    Downstream process integration

    • Reagent enters mid-stage aromatic sulfonation step, either batch or semi-continuous, frequently under alkaline conditions, followed by purification (usually via precipitation and recrystallization or ion exchange).

    Final product types

    • Acid dyes for wool, silk, and nylon
    • Reactive textile dyes
    • Pigment intermediates for aqueous ink-jet inks
    • Direct dyes for cotton and paper

    5. API Photolabile Protecting Group Manufacture for Oligonucleotide Synthesis

    Manufacturers of sophisticated oligonucleotide and nucleic acid-based APIs apply 2-Nitrobenzenesulfonyl moieties as photolabile protecting groups, facilitating temporary blockage of reactive sites, particularly in solid-phase DNA synthesis. Automation platforms require rigorous chemical traceability, and photoremovable groups must maintain high efficiency in cleavage while minimizing side reactions, as specified by nucleic acid purity standards.

    Industry compliance standards

    • US FDA 21 CFR Part 820 (QSR for medical device reagents)
    • ISO 13485 for medical and diagnostic oligonucleotides
    • USP <1047> Oligonucleotide Drug Products guidelines
    • GMP-compliant batch documentation per ICH Q11

    Typical usage ratio

    • 1.0–1.2 equivalents per targeted nucleoside or phosphoramidite residue; optimized for split-and-pool synthesis scales and automated deprotection by photolysis. Minor excess ensures complete capping without excess photochemistry side products.

    Downstream process integration

    • Protecting group installed at the protected nucleoside addition step; subsequently removed via UV irradiation post-chain assembly, followed by HPLC purification of the oligonucleotide product.

    Final product types

    • Photocaged DNA/RNA oligonucleotides
    • Diagnostic probes for PCR and qPCR
    • Custom antisense drug molecules
    • Gene synthesis kits

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    Certification & Compliance
    More Introduction

    2-Nitrobenzenesulfonyl Chloride: A Trusted Choice for Consistent Reactivity

    A Reliable Intermediate in the Laboratory and Industry

    After decades spent synthesizing specialized chemicals in our own plants, certain compounds have proven themselves through their stability, selectivity, and clear results. 2-Nitrobenzenesulfonyl chloride stands out as a workhorse intermediate, prized mainly for its predictable reactivity in many transformations. Our experience manufacturing it in-house with full process control lets us produce material suited for reliable yields, whether researchers are developing novel pharmaceuticals or scaling up a sulfonation process.

    Our Model and Production Values

    We manufacture 2-nitrobenzenesulfonyl chloride with CAS number 98-77-3, offering it as a fine, off-white to pale yellow powder. Rigorous in-house analysis ensures high purity—customers often receive lots with 99% minimum assay, confirmed by HPLC and NMR checks. Moisture often determines the usability of a batch for specific syntheses, so each lot passes Karl Fischer titration before release. Our packaging lines fill the product into airtight, light-protected containers and seal it under nitrogen to preserve shelf stability.

    Having watched strict quality expectations rise each year, we have upgraded our reactors, distillation steps, and precipitation lines multiple times. The end result is lower batch-to-batch variation. Processing lines are cleaned with validated protocols, critical for pharmaceutical clients working under GMP constraints. Certificates of analysis always show individual test results rather than averages from pooled samples. For professionals in the custom synthesis business, this transparency saves time and energy at the bench.

    Application Experience in Synthesis

    The value of 2-nitrobenzenesulfonyl chloride shows up most clearly in transformations that demand a mild yet highly chemoselective sulfonylating agent. Our customers report the most success in amine and alcohol protection, where the 2-nitrobenzenesulfonyl (nosyl) group offers predictable cleavage behavior. Unlike with less robust alternatives, our material performs reliably in the installation of the nosyl group without undesired side products. That reliability gives synthetic chemists control, especially with sensitive or multi-step pathways.

    This chemical finds steady roles in the synthesis of pharmaceuticals, particularly for building block protection and deprotection. It features in strategic routes for beta-lactam antibiotics, sulfonamides, and even certain agrochemicals. Our technical team has helped customers optimize processes for gram to multi-kilogram conversion, often saving reaction time or purifications through careful adjustment of stoichiometry or solvent system. The high assay and absence of trace organic acids in our product cut down on side reactions.

    Even in the hands of experienced chemists, inconsistent raw materials add risk. Impure sulfonyl chloride tends to yield unwanted over-reactions or releases acid that damages expensive substrates. Because we synthesize at scale, impurity levels—like dinitrobenzenesulfonic acids—fall well below problematic thresholds. The result is cleaner product isolation, improved downstream crystallization, and higher overall yields.

    Comparisons with Similar Sulfonyl Chlorides

    Among sulfonyl chloride reagents, 2-nitrobenzenesulfonyl chloride demonstrates a balance of reactivity and mildness. While tosyl chloride (p-toluenesulfonyl chloride) offers higher basicity, it often results in side reactions during deprotection steps, especially with delicate nucleophiles. Our product features an electron-poor aromatic ring, making the sulfonylation reactions milder and less prone to forming over-protected byproducts. Many customers describe an easier work-up and purification as a direct benefit.

    Chlorination and nitro group introduction remain tightly controlled in our reactors, avoiding excess chlorination that can result in a higher content of undesirable dichlorides. By direct comparison, benzenesulfonyl chloride lacks the strong electron-withdrawing nitro group at the ortho position. This difference means benzenesulfonyl chloride generates stronger acid during certain coupling steps, which sometimes damages sensitive substrates. Our technical support group has guided synthetic chemists in choosing 2-nitrobenzenesulfonyl chloride for improved selectivity and better downstream conversions in multi-step sequences.

    Any choice depends on the desired balance of reactivity, stability, and cleavage conditions. We welcome direct discussions about targets and can provide detailed technical feedback based on data from our QC lab and feedback from hundreds of scale-up projects. We have often run experiments side-by-side with other sulfonylating agents in our own labs, finding that overall purity and crude reaction profiles favor 2-nitrobenzenesulfonyl chloride in complex multi-component coupling steps.

    Integrating Into Pharmaceutical and Industrial Syntheses

    Large players in active pharmaceutical ingredient (API) synthesis demand not only consistency but robust regulatory documentation and traceability. Our process records stretch back years, supporting regulatory filings and ongoing customer audits. We offer DMF writing support for our 2-nitrobenzenesulfonyl chloride. Access to full traceability—from raw starting materials, through synthetic steps, to batch records—is standard for every bulk order.

    Pharmaceutical synthesis often cannot tolerate unpredictable impurities. Over the years, our technical group has worked closely with process teams to document effects of micro-impurities—cutting down on failed runs and improving safety by eliminating unpredictable exotherms. By keeping nitro and sulfonyl precursor streams free from contaminants, we help pharmaceutical partners minimize downstream purification costs and avoid batch recalls.

    For those working in agrochemical or specialty dye manufacture, requirements differ, but purity remains critical. In multi-step dye synthesis, a consistent starting reagent prevents color variation in end products. In crop protection compounds, side products could lead to unwanted biological activity. The experience of fielding customer reports and troubleshooting their problems has driven our improvements as much as our own QC data.

    Key Practical Differences from Bulk Commodity Grades

    Some manufacturers opt for volume over precision, pushing out tonnage grades with minimal end-use consideration. We operate leaner, focusing on tighter specifications and minimizing batch variability. This approach delivers fewer surprises during process transfer from laboratory to pilot scale. Years ago, a colleague who switched to bulk-grade 2-nitrobenzenesulfonyl chloride reported sharp drops in coupling yields and persistent orange tints in their product—classic signs of unstable impurity levels. Our protocols, in contrast, limit colored byproducts to undetectable levels.

    Cost-cutting in raw materials sometimes brings unwanted residues or increases water content, causing samples to degrade sooner than expected. By investing in dedicated, closed equipment for nitro-sulfonyl chemistry, we eliminate contamination risks from cross-products. This pays off not only in higher yield but in safety: accidental mixing of chlorinating agents with wrong precursors can cause runaway reactions or hazardous emissions. With dedicated lines and operator training, we have avoided contamination recalls and reduced plant downtime.

    Challenges and Solutions in Handling 2-Nitrobenzenesulfonyl Chloride

    One tradeoff with this compound is its sensitivity to moisture and light. Exposing open containers leads to partial hydrolysis, which releases hydrochloric acid and generates sulfonic acid, often resulting in sticky, unusable materials. Our filling area operates under dry nitrogen, and operators check ambient humidity hourly to preserve integrity from production line to outgoing shipment. Every batch comes with clear best-handling practices, and our technical support addresses on-site storage questions, helping customers set up desiccant cabinets or track shelf life.

    Many chemists request the product in specific mesh sizes suitable for their reactors, or in micro-batch packaging for rapid handling under glove box or Schlenk line conditions. Our packaging crew supports requests for bottle, drum, or even custom-sealable liner sizes. The feedback loop between our field support and production team means even unusual requests—such as screen-printed safety warnings for international shipping—have become routine.

    Safe, repeatable product usage matters to us as much as to the customer. Past experience with less reputable sources has shown that even minor contamination or container degradation leads to inconsistent reactivity or operator exposure. Over time, we've tracked shipment conditions, packaging incidents, and recommended handling upgrades, improving product reliability every year.

    The Role in Modern Chemical Development

    Research chemists increasingly design routes that minimize waste or hazardous byproducts. The clean reaction profile of 2-nitrobenzenesulfonyl chloride means less need for reprocessing or energy-intensive purification steps. Feedback from academic labs often focuses on the lower emission of acidic gases during reaction and cleavage stages. Our own lab development studies consistently show one of the industry’s lowest levels of total organic impurities, helping support environmental, health, and safety goals.

    Several times, our teams have been called to help resolve stuck syntheses in new material research. Purity-sensitive coupling or protection reactions can fail because of trace organics or unreacted starting material. Technical troubleshooting with our 2-nitrobenzenesulfonyl chloride, tracked against lot records and impurity studies, pointed to out-of-spec input many times. Using validated supply allowed for rapid, predictable reaction setup, confirming the stability of the protected intermediates.

    For industrial customers pursuing ISO or other environmental accreditations, we developed documentable tracking from precursor chemical sourcing through to batch certificate. Such documentation supports compliance and provides assurance both for internal and regulatory audits. Modern plant engineers demand this level of oversight before considering new vendors, and our willingness to open records for customer review sets industry benchmarks. This transparency provides the trust needed for long-term supply agreements.

    Real-World Impact: Lessons from Practice

    Decades of customer feedback has taught us how end-users apply 2-nitrobenzenesulfonyl chloride across the world. One R&D partnership in Southeast Asia involved shifting a specialty pharmaceutical process from benzenesulfonyl chloride to our product, reducing reaction byproducts and simplifying downstream crystallization. Another large-scale order for a European dye works prompted us to refine our drying parameters, after technical managers flagged color issues linked to slight increases in moisture content.

    We've seen how mid-stream chemistry can derail if an intermediate’s stability drops. Several years ago, a food additive production group nearly lost a season’s worth of downstream product due to a contaminated supply from an unknown third party. Upon switching to our fully documented lots and consulting on proper storage, their operation saw both higher reliability and fewer shutdowns for reprocessing. Over time, these lessons shape our focus: not only producing a commodity, but actively supporting its best performance in the customer’s setting.

    Our own in-house development work uses the same product we send to customers—not a select reserve, but the same batch and process. Failures, side reactions, or handling difficulties translate directly into production or packaging changes on the line. In one example, switching container lining material based on feedback from northern European facilities eliminated an off-odor issue in delicate syntheses. Tighter packing and desiccant upgrades followed an uptick in tropical climate complaints. This kind of two-way information flow keeps both us and our customers ahead of unexpected problems.

    Supporting Future Needs in Sulfonyl Chemistry

    As synthetic methods and target molecules become more sophisticated, control over intermediate quality drives process success. Our commitment means ongoing investment in process analytics, staff training, and rapid customer response. Each lot of 2-nitrobenzenesulfonyl chloride we ship tells a story of incremental improvement, real-world feedback, and unwavering insistence on traceable purity.

    Academic, pharmaceutical, and fine chemical groups frequently ask about managing scale-up risk—especially for pilot batches ahead of full commercial runs. We work closely with chemists to assess compatibility and optimize batch sizes, and our QC and documentation support eases their transfer to regulated plant productions. When side-by-side trials reveal subtle performance differences, we analyze the data in detail—helping customers choose the better tool for their chemical targets. This consultative approach reflects our roots in hands-on chemistry.

    There is rarely a “one size fits all” answer to reagent selection. Some projects benefit from higher purity and specialized handling; others value rapid, local delivery or custom package sizing. Our flexible plant set-up allows for quick adaptation to these different end-user needs, within the bounds of robust, validated process controls. Reluctance to compromise on incoming material specifications, combined with supporting evidence from decades of plant and customer data, gives process chemists the confidence to proceed without unpleasant surprises during critical production campaigns.

    Why End-Users Rely on Consistent Supply Chains

    Chemical manufacturing relies on trust—not just in certificates, but in repeatable success, consistent material behavior, and open dialogue about potential pitfalls. Customers sometimes describe frustration with non-technical providers who can’t address issues beyond standard paperwork. We assign technical managers with hands-on plant and synthesis experience to every major account; direct conversations about reactivity, handling, and trouble-shooting sharpen our understanding each year.

    We recognize the critical pain points for our market—delays due to shipping damage, long customs holds, or unexpected purity drifts at transit warehouses. For global customers, we offer shipment with added logistic controls, including real-time tracking for sensitive orders and climate-controlled containers for long ocean routes. If problems arise, we engage directly and investigate root causes rather than issuing standard apologies.

    Technical partnerships built through years of supply enable us to anticipate—rather than just react to—market and process challenges. In a world where rapid change is the norm, and synthetic requirements grow more demanding, this commitment ensures 2-nitrobenzenesulfonyl chloride remains a reliable option for customers ranging from specialty chemical startups to major pharmaceutical firms. We invite conversations that lead not just to transactions, but to better processes and safer, more efficient chemistry around the globe.

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