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4-Chloro-3-Nitrophenyl Methyl Sulfone

    • Product Name 4-Chloro-3-Nitrophenyl Methyl Sulfone
    • Alias 4-Chloro-3-nitro phenyl methyl sulfone
    • Einecs 'EINECS 414-120-6'
    • 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

    372620

    Product Name 4-Chloro-3-Nitrophenyl Methyl Sulfone
    Cas Number 52514-34-6
    Molecular Formula C7H6ClNO4S
    Molecular Weight 235.64 g/mol
    Appearance Light yellow to yellow powder
    Melting Point 112-116 °C
    Solubility Slightly soluble in water; soluble in organic solvents such as DMSO
    Purity >98% (typical)
    Smiles CS(=O)(=O)C1=CC(=C(C=C1)Cl)[N+](=O)[O-]
    Inchikey JPXYJKRKFWXSNU-UHFFFAOYSA-N
    Synonyms Methyl 4-chloro-3-nitrophenyl sulfone
    Storage Temperature Store at 2-8°C, protected from light and moisture

    As an accredited 4-Chloro-3-Nitrophenyl Methyl Sulfone 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 25 grams of 4-Chloro-3-Nitrophenyl Methyl Sulfone, sealed with a screw cap and hazard labeling.
    Shipping 4-Chloro-3-nitrophenyl methyl sulfone is typically shipped in tightly sealed containers to prevent moisture and contamination. It should be kept in a cool, dry place and handled with care. Shipping complies with all relevant hazardous material regulations, including appropriate labeling, documentation, and protective packaging to ensure safe transport.
    Storage 4-Chloro-3-Nitrophenyl Methyl Sulfone should be stored in a tightly sealed container in a cool, dry, and well-ventilated area, away from sources of ignition, heat, moisture, and incompatible substances such as strong oxidizing agents. Avoid exposure to direct sunlight. Proper labeling and containment are essential to prevent leaks or contamination. Store at room temperature and follow all relevant safety protocols.
    Application of 4-Chloro-3-Nitrophenyl Methyl Sulfone

    Applications of 4-Chloro-3-Nitrophenyl Methyl Sulfone in Industrial Manufacturing

    4-Chloro-3-Nitrophenyl Methyl Sulfone serves as a specialty intermediate across selected technical fields. Our production consistently meets industrial requirements, supporting defined synthesis routes in high-value downstream segments. Each application below addresses specific use cases, compliance, dosage guidance, processing methods, and typical finished goods.

    1. Agrochemical Intermediate Synthesis

    Major agrochemical producers employ this compound as a custom intermediate in the preparation of advanced herbicides and fungicides. The electron-withdrawing nitro and sulfone groups enable precise substitution reactions, supporting synthesis pathways for selective pesticides. Our material's consistency and purity remain critical for subsequent coupling and condensation steps, ensuring target yield and activity in crop protection product development.

    Industry compliance standards

    • GB/T 19001-2016/ISO 9001:2015 Quality Management System
    • China Pesticide Registration Standards
    • EU REACH (Registration, Evaluation, Authorisation and Restriction of Chemicals)
    • EPA 40 CFR Part 180 (USA residue tolerance in food)

    Typical usage ratio

    • 5–30% in intermediate coupling reactions, with dosage tailored to target active compound synthesis and scaled based on batch size and final molecule structure requirements.

    Downstream process integration

    • Enters post-nitration in the aromatic sulfone synthesis line.
    • Acts as a building block in the primary condensation step with parent amines or phenols.
    • Subsequent purification integrates into the crystallization stage of active technicals.

    Final product types

    • Pre-emergent herbicide technical concentrates
    • Systemic fungicide intermediates
    • Selective insecticide precursor molecules

    2. Pharmaceutical Intermediate for Active Ingredient Preparation

    Pharma manufacturers utilize this sulfone derivative as a building block in syntheses of targeted APIs, particularly where specific aromatic substitution enhances pharmacological profiles. Its reliable reactivity profile, consistent particle size, and high-purity specification support strict downstream GMP protocols, allowing for reproducible batch synthesis and traceable process validation during multi-step API manufacturing routes.

    Industry compliance standards

    • ICH Q7: Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP/NF (United States Pharmacopeia/National Formulary) Reference Standards
    • Chinese Pharmacopoeia 2020 Edition General Chapter 4201 (Impurity Control)
    • EudraLex, Volume 4 GMP Guidelines (EU)

    Typical usage ratio

    • 2–20%, calculated as a molar equivalent to upstream reactants. Scaling depends on specific process route and final API target.

    Downstream process integration

    • Functions as an initial aromatic source in C-nitro or C-chloro coupling reactions in the synthetic API process.
    • Enters amidation or reduction stages prior to API isolation and final purification.

    Final product types

    • Oral anti-infective API intermediates
    • Oncology drug precursor compounds
    • Pharmaceutical grade fine chemicals for regulated export markets

    3. Dye and Pigment Synthesis

    Dye manufacturers adopt this sulfone as a functionalized aromatic feedstock to introduce reactive anchor points for chromophore assembly. The compound’s chloro-nitro groups facilitate introduction of color-giving azo or anthraquinone bridges. Companies specify tight quality controls to ensure batch-to-batch uniformity in shades and stability in textile and industrial applications.

    Industry compliance standards

    • Oeko-Tex Standard 100 for textile chemical safety
    • EN 71-3:2019 (Heavy metal content in dyes, EU)
    • ISO 9001:2015 (Quality control in fine chemical synthesis)
    • REACH Annex XVII (Regulation of restricted azo dyes)

    Typical usage ratio

    • 8–40% as an electrophile in diazotization or coupling reaction, with tuning based on chromophore structure and hue intensity targets.

    Downstream process integration

    • Feeds into early-stage colorant core formation and substitution reactions.
    • Applied before sulfonation or metallization steps in dye manufacturing.
    • Participates in closed-loop solvent and off-gas handling to control process emissions.

    Final product types

    • Sulfonated reactive textile dyes
    • Azo pigment dispersions for plastics
    • Industrial colorants for coating applications

    4. Electronic Chemicals for Specialty Polymer Manufacture

    Producers of high-performance engineering polymers use this chemical to introduce stability and electronic rigidity in advanced monomer formulations, especially in the electronics sector. The compound enhances polymer backbones for improved thermal resistance and dielectric performance. Downstream manufacturers benefit from consistent impurity profiles to meet stringent device reliability requirements in microelectronic and optoelectronic assembly.

    Industry compliance standards

    • RoHS Directive (EU 2011/65/EU, restriction of hazardous substances)
    • IEC 61249-2-21 (Base materials for electronic interconnections)
    • ISO 14001:2015 Environmental Management (for production system tracking)
    • UL 94 for polymer flammability testing

    Typical usage ratio

    • 2–12% as a comonomer or chain modifier in specialty polymer synthesis, adjusted to resin design and targeted mechanical properties.

    Downstream process integration

    • Blended with phenolic or epoxide monomers during bulk polymerization.
    • Incorporated prior to casting, extrusion, or film formation and pre-polymerization blending.

    Final product types

    • Printed circuit board (PCB) laminates and prepregs
    • High-temperature engineering plastics
    • Optically clear films for displays and optoelectronic parts

    5. Custom Synthesis for Fine Chemical Production

    Contract manufacturers and specialty chemical producers source this molecule to unlock precise aromatic sulfone chemistry in multi-step fine chemical routes. Its defined reactivity aids in generating rare sulfone, nitro, or chloro containing fragments, supporting creation of advanced functional chemicals required in flavor, fragrance, or specialty additive sectors. The batch lot and full-traceability records we supply meet high expectations for contract QC traceability.

    Industry compliance standards

    • ISO 9001:2015 Quality Management in contract manufacturing
    • STRICT adherence to NDA/Confidentiality-protected customer protocols
    • REACH compliant MSDS and packing labelling for EU transport
    • Japan Chemical Substances Control Law (CSCL) notification where applicable

    Typical usage ratio

    • 1–25% contingent on custom product molecular design; accurate based on stoichiometry requirements for target specialty structure.

    Downstream process integration

    • Used in controlled aromatic substitution or condensation reactions tailored for custom molecule synthesis.
    • Incorporated directly in the building-block assembly, enabling yield improvement in multi-step fine chemical processes.
    • Managed with tailored waste stream and byproduct minimization to ensure sustainable production.

    Final product types

    • Aromatic sulfone intermediates for further derivatization
    • Synthetic fragrance ingredients
    • High-purity additives for polymer or lubricant formulation
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    Certification & Compliance
    More Introduction

    4-Chloro-3-Nitrophenyl Methyl Sulfone: A Manufacturer’s Perspective

    Introducing a Precision Intermediate for Specialty Synthesis

    Experience in the chemical industry offers a front-row view of how demand for fine organic building blocks has evolved. Among the myriad of specialty compounds, 4-Chloro-3-Nitrophenyl Methyl Sulfone stands out in our catalog, valued for its stability and selectivity across several synthetic contexts. Our workshops run it through demanding quality metrics, ensuring consistent crystalline properties. Every batch meets purity expectations essential for research and production in advanced pharmaceuticals, agrochemical discovery, and dyestuff developments.

    Understanding the Material: Core Applications

    In our laboratory, 4-Chloro-3-Nitrophenyl Methyl Sulfone draws chemical architects for its reliable electron-withdrawing sulfone and nitro groups. These groups influence reactivity, making the compound a powerful moiety for stepwise elaboration in both academic and commercial projects. Most requests come from teams working to build heterocycles for first-in-class biologically active molecules. Chemists recognize that this intermediate brings more than mere structural novelty; it offers a defined reactivity profile, reducing off-target reactions and helping streamline purification.

    In process development, the compound’s predictable melting point and solubility behavior help reduce troubleshooting. Its absence of labile functionalities means we rarely encounter batch-to-batch variability that plagues other nitroaromatics. Approved for use in multiple regulated environments, its reliable profile has encouraged further bridge-building into API synthesis campaigns.

    Model Consistency and Batch Quality

    We keep a steady eye on reproducibility. 4-Chloro-3-Nitrophenyl Methyl Sulfone is not just a lot number in our inventory; it represents a carefully built model of quality control. Each batch undergoes identity confirmation through NMR, LC-MS, and IR checks. Low-level impurities typically fall below thresholds for advanced synthesis, a direct result of rigorous process optimization. Chemists in our QC team understand the significance of these standards, especially as downstream transformations often depend on such starting materials for high-yielding, clean reactions.

    Anecdotes from customers highlight the convenience of our consistently high-purity material. Some of these teams mention shortened project timelines and reduced purification workloads, outcomes only possible with fewer side-products and negligibly low trace contaminants. Our experience confirms that taking short-cuts on purification or flexibility in processes quickly triggers inconsistencies, so we champion routine and controlled parameters above all.

    Specifying What Matters: Purity and Handling

    Hands-on production teaches that specifications can’t rest on paper guarantees. Commercial, kilo-scale orders demand the same faithful adherence to spec as 10-gram research packs. Our user base—whether contract research or in-house development crews—counts on solids without clumping, discoloration, or excessive dust that could compromise measurements or cause unsafe exposure. Hygroscopicity tests inform the storage guidance we pass on; the compound’s well-packed crystalline form helps minimize environmental moisture uptake, and direct handling experience tells us the additional nitrogen group imparts more physical stability than most sulfone benchmarks.

    Our trained staff carefully avoid static buildup during weighing—a small detail, but one with a real impact when transferred to high-throughput experimentation platforms. As a result, the compound supports automated dosing lines, which feature wider in pharma pilot plants. This real-world compatibility doesn’t get captured in spec sheets. Years of product handling, drying techniques, and packaging adjustments permit precise repetition every cycle.

    Differentiation from Other Nitroaromatics and Sulfones

    Clarifying the merits of 4-Chloro-3-Nitrophenyl Methyl Sulfone sometimes obliges a quick chemistry lesson. Nitroaromatics share a family resemblance, but nuances set this specific intermediate apart. Incorporating a chloro substituent at the para position directs downstream reactivity, boosting selectivity for specific Suzuki or nucleophilic aromatic substitutions. Synthetic schemes that pivot on such reactivity often see fewer byproducts and increased yields compared to analogues like 4-nitrophenyl methyl sulfone, which misses the electron-shuffling chlorine atom.

    Other sulfone intermediates, though structurally similar, can lack the simultaneous electron-rich and electron-deficient environment created by the joint nitro and chloro pairing. This feature expands the chemical window, letting medicinal chemists cross into transformations usually off-limits for conventional aryl sulfones. Comparing with 3-nitrophenyl methyl sulfone or even multi-substituted analogues, our in-house trials and customer feedback confirm this combination uniquely enables certain regioselective syntheses. Over years of campaigns, our observation tracks with these reports: when selectivity matters, most teams circle back to this compound after running pilot reactions on others.

    Supporting Focused Synthesis Routes

    Optimization efforts in chemical manufacturing gain a boost when supplied intermediates behave as expected. Experienced teams rely on reactions that don’t drift from standard conditions—whether scaling up a Grignard pathway, aromatic substitution, or esterification. The properties of 4-Chloro-3-Nitrophenyl Methyl Sulfone, including its resistance to reduction and steady solubility in common polar solvents, help steer synthetic sequences toward robust, high-yield results. As a manufacturer, we invest in early-stage work-up protocols alongside our clients to cut the learning curve on new processes.

    The compound’s compatibility with established protecting group strategies lets researchers and process chemists innovate without roadblocks. We have consulted with external teams experimenting with sulfone deprotection or targeted photolytic releases; each time, the crystalline stability and clean reactions support repeatable outcomes. Testimonies from groups moving toward scale-up have frequently credited our quality with simplifying their transfer from milligram screens to pilot or manufacturing scale.

    Sustainability and Responsible Sourcing

    Modern chemical production cannot overlook the environmental and safety aspects surrounding specialty intermediates. We invest in responsible sourcing of starting reagents. Our sulfur dioxide and aromatic feedstock come from established, certified supply streams, with full traceability to minimize risk. Waste streams from the synthesis of 4-Chloro-3-Nitrophenyl Methyl Sulfone are routed through approved treatments to ensure regulatory harmony and workplace safety.

    We continuously audit both energy consumption and solvent cycles for greener alternatives. Where text-book syntheses may rely on chlorinated solvents or aggressive oxidizers, we routinely review and adapt our processes to drop environmental burden where feasible, without sacrificing product performance. These investments in sustainability present both a responsibility and a business requirement, as more formulators and end-users request both supply chain transparency and concrete actions to reduce chemical waste.

    As a direct manufacturer, we take feedback from our warehouse and shipping teams as seriously as from our lab staff. The durability of the compound’s packaging, resilience to accidental impact, and the clarity of labeling help keep overall process safety uncompromised. Industry requirements demand more than compliance; our stake in responsible handling sets a model many downstream partners now expect us to help enforce up the value chain.

    Delivery, Packaging, and Custom Orders

    From our vantage point, a significant part of product satisfaction does not end with synthesis. Controlled drying conditions and packaging lines ensure batches remain free from excess particulate and moisture. In response to research and pilot plant customers, our workflow has evolved from standard drums to smaller, single-use liners and moisture-barrier bags. This helps teams handling only a few hundred grams avoid product caking or losses, while also supporting easy access for large-scale refills in process development settings.

    Custom order requests have become frequent. We accommodate needs ranging from high-load, multi-kilo deliveries for industrial pilot runs to small vials for boutique research. Each shift, our staff double-check weights and inspect seals, adopting the practice that an overlooked tear or improper cap will multiply issues down the line. As a manufacturer, solving these small but persistent problems eliminates backlogs and upholds the level of trust we have with repeat partners.

    Internal logistics staff coordinate with couriers and bulk freight providers, ensuring regulated documentation and rapid traceability from the moment a request enters our system to dispatch. Many of our clients report fewer interruptions related to transit damage compared to past experiences with less robust packages. Labeling ties into batch-level records, supporting full backward tracing if any questions about specifications or compliance standards ever arise.

    Regulatory and Research Environment

    Working on this compound, extensive collaborative cycles with regulatory teams have clarified many functional requirements. 4-Chloro-3-Nitrophenyl Methyl Sulfone is not a controlled substance, which enables smoother transit across most commercial and research borders. Still, we maintain documentation on heavy metals, residual solvents, and genotoxins in line with ICH and Reach guidelines where assay results verify compliant levels.

    We coordinate frequently with clients in contract manufacturing and academic centers working on pre-clinical targets. Project leads count on our prompt documentation: certificates of analysis, material safety records, and—crucially—detailed transparency about any process changes. Our approach builds confidence, not by over-promising, but by maintaining the discipline to back technical claims with documentation rooted in verified results.

    Support and Continuous Improvement

    Technical support draws from practical experience with the material, not just a reference to standard guidelines. Research labs reach out seeking reaction optimization, not only because we know the core synthesis, but because we’ve seen pitfalls in failed attempts. We regularly troubleshoot setbacks during nucleophilic substitutions or coupling protocols, sharing what our team has already overcome in upstream and scale-out adjustments. Over years, this approach shortens feedback cycles and prevents repeated errors, particularly for less common scale-up issues where literature falls short.

    Chemists want real engagement, not scripted scripts. Sharing practical solutions, backed by internal experiments and scaled trials, proves more valuable than long lists of theoretical protocol steps. Teams working with demanding regulatory or technical timelines benefit from these exchanges, where manufacturing experience closes the gap between raw material supply and successful product development.

    Outlook: Meeting Emerging Industry Trends

    Innovation cycles grow sharper as pharmaceutical and fine chemical companies pivot toward faster project launches. 4-Chloro-3-Nitrophenyl Methyl Sulfone serves as a versatile and reliable intermediate with the adaptability to meet new challenges. Industry analysts project growing interest in substituted aryl sulfones for next-generation drug candidates. In response, our R&D and production engineers engage in regular process reviews, preparing for increased scale demands and new technical collaborations.

    As new synthetic targets emerge, our staff partners with external method developers to validate 4-Chloro-3-Nitrophenyl Methyl Sulfone’s place in cutting-edge synthetic flows, anticipating shifts in selective functional group transformations and late-stage elaboration. Research feedback suggests increasing exploration of this intermediate in photoredox and palladium-catalyzed methodologies. Our continued investment in scale-flexible manufacturing lines ensures rapid responses as these advanced protocols progress from discovery to pre-clinical supply.

    Field knowledge tells us that reliability, transparency, and technical familiarity with our product outperform generic or commodified inventories. We work to ensure that each shipment delivers on these expectations, positioning 4-Chloro-3-Nitrophenyl Methyl Sulfone as a trusted solution for project teams demanding more than off-the-shelf performance. By continually refining our approach—through ongoing dialogue with chemists, active data gathering, and visible commitment to environmental and operational standards—we support genuine progress for our partners across research and industry.

    The Manufacturer’s Difference

    Manufacturing specialty chemicals means living with the results of every synthesis and shipment, not just pushing paperwork or moving boxes. Our years in this business, handling and delivering 4-Chloro-3-Nitrophenyl Methyl Sulfone, have built up more than just operational know-how. The connections formed with scientists and engineers inform every production tweak and support call. Experience proves that every detail matters, from equipment calibration and fine-tuned purification, all the way to customer advice on reaction troubleshooting and scale-up support.

    As new applications for this intermediate continue to emerge, our proactive approach—rooted in practical experience and ongoing improvement—anchors its reputation as a preferred choice across demanding arenas. Our approach delivers more than a chemical sample: it delivers a partner committed to reliability and technical integrity where every batch, and every reaction, can move forward without hesitation.