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1-(Methylsulfonyl)-4-Nitrobenzene

    • Product Name 1-(Methylsulfonyl)-4-Nitrobenzene
    • Alias 4-Nitrophenyl methyl sulfone
    • Einecs 220-509-8
    • 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

    720075

    Iupac Name 1-methylsulfonyl-4-nitrobenzene
    Molecular Formula C7H7NO4S
    Molecular Weight 201.20 g/mol
    Cas Number 1610-49-7
    Appearance Yellow solid
    Melting Point 117-120°C
    Solubility In Water Low
    Smiles CS(=O)(=O)C1=CC=C(C=C1)[N+](=O)[O-]
    Pubchem Cid 17839
    Synonyms 4-Nitrophenyl methyl sulfone
    Storage Conditions Store in a cool, dry place

    As an accredited 1-(Methylsulfonyl)-4-Nitrobenzene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 250g clear amber glass bottle with tamper-evident cap, labeled with product name, purity, safety pictograms, and handling instructions.
    Shipping **Shipping Description for 1-(Methylsulfonyl)-4-Nitrobenzene:** This chemical is shipped in tightly sealed, chemical-resistant containers. It is protected from moisture, heat, and direct sunlight. All packages are clearly labeled with hazard information. Shipping complies with relevant regulations for potentially hazardous organic compounds, and transport is handled by certified chemical carriers to ensure safety.
    Storage Store **1-(Methylsulfonyl)-4-nitrobenzene** in a tightly sealed container, kept in a cool, dry, and well-ventilated area away from direct sunlight and incompatible substances such as strong oxidizers or reducers. Ensure storage at room temperature and protect from moisture. Clearly label the container and keep it away from sources of heat, flame, or ignition. Follow all standard laboratory chemical storage protocols.
    Application of 1-(Methylsulfonyl)-4-Nitrobenzene

    Applications of 1-(Methylsulfonyl)-4-Nitrobenzene in Industrial Manufacturing

    As a direct manufacturer, we provide high-purity 1-(Methylsulfonyl)-4-Nitrobenzene used in several established sectors. Each application below outlines how customers use our product for advanced synthesis, illustrating relevant compliance, process positioning, and the spectrum of downstream goods.

    1. Pharmaceutical Intermediate for Sulfonamide Drugs

    1-(Methylsulfonyl)-4-Nitrobenzene serves as a specialized intermediate in the synthesis of sulfonamide-based active pharmaceutical ingredients (APIs). The nitro and methylsulfonyl groups enable selective substitution steps, particularly in the manufacture of antimicrobial drugs. Downstream laboratories operate under cGMP protocols for API synthesis, utilizing our material in the stage prior to the reduction and sulfonation steps. Integration requires validated solvent washing to ensure impurity control, meeting stringent pharmacopoeia monograph specifications for residual solvents and starting material purities.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice Guide for Active Pharmaceutical Ingredients
    • Ph. Eur. and USP purity specifications for residual solvents
    • 21 CFR Part 211 (FDA GMP regulations)
    • Chinese Pharmacopoeia (ChP) intermediate quality requirements

    Typical usage ratio

    • Reaction batch formulae: 0.9 – 1.3 molar equivalents, adjusted according to API route and impurity profile constraints

    Downstream process integration

    • Enter the initial aromatic substitution stage prior to reduction and coupling
    • Subject to careful monitoring in in-process QC for partial reduction/overreaction
    • Used with phase-transfer catalysts in certain advanced sulfonamide syntheses

    Final product types

    • Sulfonamide antibiotics (e.g., sulfamethoxazole intermediates)
    • Anticancer sulfonamide APIs
    • Bespoke pharmaceutical intermediates supplied for contract manufacturing organizations (CMOs)
    • Diagnostic chemical reagents for pharmaceutical research kits

    2. Agrochemical Synthesis: Herbicide Intermediates

    Major agrochemical manufacturers rely on 1-(Methylsulfonyl)-4-Nitrobenzene for constructing core building blocks in modern herbicide molecules, especially in the formation of nitro- and sulfonyl-functionalized aromatic agrochemicals. This raw material supports scalable production under strict contamination control, dovetailing with environmental regulations covering process emissions and worker safety in chemical synthesis plants. Formulators often adjust sulfonyl input ratios depending on seasonal demand and impurity drift during scale-up.

    Industry compliance standards

    • European REACH Regulation (EC) No 1907/2006 registration
    • US EPA 40 CFR Part 158 (Data Requirements for Pesticides)
    • ISO 9001:2015 Quality Management in agrochemical manufacturing
    • Chinese Ministry of Agriculture GB/T 1600-2001 (for raw material traceability)

    Typical usage ratio

    • Batch process: 10–18% by weight of total active ingredient precursor charge
    • Adjusted based on expected conversion rates and impurity loading

    Downstream process integration

    • Feeds aromatic nitration and sulfonylation reactors for key herbicide scaffolds
    • Integrated in continuous or semi-batch processes
    • Implements in-line analytical tracking for downstream purity confirmation

    Final product types

    • Precursor intermediates for triazine and sulfonylurea herbicides
    • Formulated wettable powder and granule herbicides
    • Bulk agrochemical technical concentrates
    • Off-patent herbicide intermediates for global crop protection markets

    3. Advanced Polymer and Specialty Resin Additive Manufacturing

    Polymer compounders and plastics manufacturers utilize 1-(Methylsulfonyl)-4-Nitrobenzene in the production of high-performance aromatic sulfone monomers. The functionalization delivered by the nitro and sulfonyl groups improves thermal and oxidative stability in specialty polyaryletherketone (PAEK) and polyethersulfone (PES) systems. Downstream resin producers integrate this intermediate through precise dosing in closed batch reactors, maintaining high levels of control over molecular weight distribution and crosslinking density for use in demanding electrical and filtration applications.

    Industry compliance standards

    • UL 94 Flame Classification for end-use resin safety
    • EU RoHS Directive 2011/65/EU chemical trace restrictions
    • ISO 14001:2015 Environmental Management (for closed reactor handling)
    • REACH compliant for industrial polymer additives

    Typical usage ratio

    • Monomer input: 2–7% by total monomer mass, depending on target polymer grade
    • Adjusted for end-use dielectric, strength, or thermal requirements

    Downstream process integration

    • Charged to monomer mixing tanks ahead of main chain-growth reaction
    • Used in step-growth or solution polymerization steps
    • Subject to resin dissolution and viscosity measurement at QC sample points

    Final product types

    • Performance resins for high-temperature filtration membranes
    • Polymer-based electronic housings and automotive connectors
    • Specialty coatings and flame-retardant plastic components
    • Semipermeable films for battery separators

    4. Electronic Chemicals: Synthesis of Organic Semiconducting Materials

    Fabricators of organic electronic components rely on 1-(Methylsulfonyl)-4-Nitrobenzene for the finely tuned synthesis of aromatic semiconducting cores utilized in manufacturing advanced display and sensor applications. The electron-withdrawing nitro and methylsulfonyl groups impact the donor–acceptor ratio in target molecules, assisting in band-gap engineering for organic field-effect transistors (OFETs) and light-emitting diodes (OLEDs). Downstream customers demand exceptional lot traceability, with our production aligning to electronic material QC protocols and solvent residue controls beyond standard chemical supply practices.

    Industry compliance standards

    • IEC 61249-2-21 (Restriction of halogens in electronic materials)
    • JIS C 5016:2016 (Japanese standard for organic electroluminescent materials)
    • SEMATECH protocol for organic semiconductor intermediates
    • RoHS/REACH traceability documented with each batch

    Typical usage ratio

    • Feedstock formula: 0.5–5% by weight of total organic precursor, customized for electronic grade purity and molecular design

    Downstream process integration

    • Entered at the aromatic nitration or sulfonation assembly stage for device-specific molecular scaffolds
    • Followed by purification via column chromatography or recrystallization
    • Critical for QC verification against organic contamination standards

    Final product types

    • Organic field-effect transistor (OFET) base materials
    • OLED emitter and transport materials
    • Organic photovoltaic (OPV) absorbing layer precursors
    • Chemiluminescent sensor substrate components

    5. Dye and Pigment Chemistry: Intermediate for High-Stability Colorants

    The compound is integral for dye manufacturers producing sulfone-functionalized nitroaromatic colorants. The chemical’s unique combination of sulfonyl and nitro groups enables production of dyes with superior fastness properties for textile and plastic coloration. Process operators tightly control the proportion added in dye coupling and reduction steps, with batch monitoring for hue precision and avoidance of unwanted tints from side reactions. Strict adherence to quality systems ensures that output dyes conform to health and environmental standards, especially for export markets.

    Industry compliance standards

    • OEKO-TEX® Standard 100 chemical component list for restricted substances
    • EN 71-3 Safety of Toys: Migration of certain elements (for pigment use in toys)
    • ISO 105-C06:2010 Color fastness to domestic and commercial laundering
    • ZDHHC-MRSL (Zero Discharge of Hazardous Chemicals Manufacturing Restricted Substances List)

    Typical usage ratio

    • Dye synthetic step: 3–12% by total reactant mass, adjusted to color strength and production route
    • Tighter ratio control for high-end pigment and textile applications

    Downstream process integration

    • Added during initial azo coupling or sulfonation step
    • Integral for red and yellow nitroaromatic dye development
    • Subject to in-process colorimetric analysis and residue control

    Final product types

    • Reactive and disperse dyes for textiles
    • High-purity pigments for plastics and coatings
    • Colorants for inks and digital printing media
    • Stain-resistant textile dye formulations
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    Certification & Compliance
    More Introduction

    Understanding 1-(Methylsulfonyl)-4-Nitrobenzene: Our Experience from the Factory Floor

    A Close Look at the Identity and Role of 1-(Methylsulfonyl)-4-Nitrobenzene

    As professional manufacturers with years of hands-on work synthesizing specialty benzene derivatives, we’ve come to appreciate both the versatility and subtleties of 1-(Methylsulfonyl)-4-Nitrobenzene. In the world of aromatic nitration and sulfonylation, products like this bridge the gap between common precursors and advanced intermediates for pharmaceuticals and materials science.

    The molecule, with its nitro group at the para position and a methylsulfonyl group at the other, finds use most prominently as a building block in organic synthesis. Chemists reach for it during the development of advanced intermediates for APIs or when a strong electron-withdrawing effect is required in the molecule design. The combination of nitro and sulfonyl functionalities creates unique reaction pathways, making it a reliable partner in forming further complex structures.

    Our Manufacturing Journey: Purity and Consistency Matter Most

    Running batch and continuous processes in our plants, we have always paid attention to controlling every parameter—temperature, pH, timing, and reagent quality. Impurities often cause the most headaches on the production line. Even a slight variation in purification steps shows up in downstream reactions, affecting yields or triggering off-colors in products. We run HPLC and NMR routinely, not just once at the end, to confirm the identity and purity early on. From our practical experience, customers see best performance with a product meeting or exceeding 99% purity. Less pure material often leads to unpredictable behavior.

    Maintaining batch homogeneity is not merely about following protocols but about learning when something looks off—the way the solution clears at a crucial temperature, the smell during methylsulfonyl introduction. Technicians and supervisors in the pilot hall can spot inconsistencies faster than any electronic device if you train your nose and eyes. Rather than relying entirely on data logs, we advocate for walking the synthesis rooms: holding samples up to the light, testing flow rates, and checking pH by hand. Over time, we have learned to trust these observations as much as analytical printouts.

    Specifications Driven by Practical Chemistry, Not Just Numbers

    While standard sheets list melting points, solubility ranges, and UV-vis absorbance, we value what the properties mean in a running process. For example, 1-(Methylsulfonyl)-4-Nitrobenzene provides stability under alkaline conditions and moderate heat, so it fits well in multi-step syntheses where less robust intermediates might decompose or require inert-atmosphere handling. Unlike nitrobenzenes with less polar substituents, a methylsulfonyl group brings greater solubility in polar aprotic solvents, easing handling in continuous stirred-tank reactors.

    We recommend storing the product sealed and away from high moisture, as persistent humidity can degrade even the highest purity compound over time. Although the product’s shelf stability rates favorably compared to less robust aryl-sulfonyl derivatives, good warehouse practices make all the difference between a clear yellow crystalline solid and material that clumps or sticks. This consideration emerges only after packaging and shipping hundreds of kilograms through variable climates.

    Application Insights: Fine Chemical Synthesis and Pharmaceutical Research

    Laboratories in the pharmaceutical and agrochemical industries commonly request tailored lots of 1-(Methylsulfonyl)-4-Nitrobenzene, each with nuanced expectations on impurity profiles. We have seen it put to work as a key step intermediate in the construction of new classes of kinase inhibitors, antibiotics, and photosensitive agents. The methylsulfonyl group acts as a strategic handle for further substitution through nucleophilic aromatic substitution (SNAr) or reduction pathways.

    Our partners often discuss the issue of batch-to-batch reproducibility. Over scale-up, tiny changes in reagent grade, solvent dryness, or temperature ramp rates can influence the ease of scale translation. For example, successful coupling with organometallics downstream depends upon removing certain types of trace metals or minimizing residual acids. Building this level of reliability into every shipment requires auditing not only raw material suppliers but also validating every solvent cut and filtration stage within our own facility.

    We see a clear divide between R&D procurement for milligram labs and pilot plant runs preparing kilogram lots. In the research setting, a premium falls on lot-to-lot analytical transparency and flexibility with custom packaging or documentation. Larger scales put the spotlight on material flow, packaging stability, and minimizing static buildup or caking—practical logistics sometimes overlooked in purely academic chemistry. We work closely with both groups, adjusting fulfillment strategies based on whether their end use centers on method validation or full-scale run-up.

    Comparing Similar Aromatic Nitro Compounds: What Sets It Apart

    Plenty of nitrobenzene derivatives populate the shelves of major chemical suppliers. The addition of a methylsulfonyl group brings unique reactivity and physical traits. While nitrobenzene itself or its halogenated relatives (such as 4-chloronitrobenzene) serve as core intermediates for numerous syntheses, the methylsulfonyl version stands out due to its balance of electron-withdrawing strength and synthetic accessibility. In coupling and nucleophilic aromatic substitution reactions, it opens up possibilities not easily obtainable with less polar or less reactive counterparts.

    From a handling viewpoint, products carrying sulfonyl groups generally blend well with strong bases and remain stable during most amination or alkylation steps. Halide-substituted nitrobenzenes come with additional safety and waste handling concerns due to the risk of forming toxic byproducts or being subject to stricter regulatory controls. The methylsulfonyl group brings fewer complications and still delivers high reactivity.

    Differences in odor and dust generation, often dismissed as minor, become important on the production and warehouse floors. Many nitroaromatics have a sharp, persistent smell or produce fine dust, which creates discomfort and waste during large-scale transfers. Our team monitors these characteristics and works with packaging suppliers to minimize worker exposure and loss during repackaging or drum filling.

    Meeting Modern Quality and Regulatory Demands

    Chemicals for advanced synthesis now face higher standards from customers, regulators, and auditors. As a manufacturer, we respond by implementing batch traceability, clean-in-place regimes, and adopting green chemistry principles to reduce mother liquor and rinse waste. We work toward minimizing wastewater and solvent emissions at every step, following internal and external guidelines. Each production run generates an electronic record of every addition, filtration, and packaging event. This enables full transparency when questions arise about compliance or impurity origins.

    One aspect often overlooked relates to residual solvents and aldehydes—regulatory frameworks like ICH Q3C set clear limits, but in our view, it makes sense to exceed these targets whenever practical. We run GC-MS screening as standard, not as an afterthought, so our customers move forward in their own audits with confidence. The shift toward pharmaceutical and food-chain precursor applications means placing a premium on documentation and rapid response to questions about batch histories.

    Lessons Learned: Customer Feedback Drives Real Improvements

    The most valuable suggestions rarely come from boardroom meetings. Feedback from technicians and operators using 1-(Methylsulfonyl)-4-Nitrobenzene on the lab bench or in the pilot plant has shaped many upgrades, from tamper-proof packaging to more legible QR labeling. Operators in high-throughput screeners remind us that presentation—how easily a sample can be weighed, dissolved, or transferred—matters as much as the underlying purity.

    Challenges such as caking in humid conditions, inconsistent color in varied light, or slow dissolution in certain solvents have prompted us to refine drying and milling steps. When a researcher notices a color shift in a sample stored improperly, we investigate the batch, trace the storage conditions, and alter our packaging. These details, overlooked by resellers, hold enormous significance for final users who rely on every gram in precision synthesis.

    Connecting with Science and Industry: Transparency Builds Trust

    Trust between manufacturer and user forms from honesty, quick response, and open sharing of production details. We don’t outsource these functions. Each inquiry received about our 1-(Methylsulfonyl)-4-Nitrobenzene receives a response from a person who’s physically seen, tested, and packaged the product, not a remote sales office. Real-life insights into why a certain lot smells different, or why a sample dissolves slower in acetonitrile, come straight from our manufacturing staff.

    Raw analytical data files are available upon request, and we maintain open communication regarding changes to process, packaging, or specification adjustments. This transparency founds long-term partnerships. In an environment where regulations tighten yearly and end users bear increasing accountability, we understand the pressure to document, audit, and risk-assess each raw material from lab to factory.

    Industry Conversations: Adapting to New Demands

    Recent years have brought shifts in demand. As new synthetic pathways emerge—where the challenge is not merely yield but traceability and containment—1-(Methylsulfonyl)-4-Nitrobenzene has moved beyond being a niche intermediate. Sustainability concerns influence not just end-products but upstream choices, too. We’ve pivoted toward greener production processes, replacing older oxidizers and minimizing waste streams. Our initiative to recover and reuse solvents demonstrates this commitment, as well as investing in vent scrubbers that exceed basic environmental guidelines.

    Customers working on routes for green pharmaceuticals or biodegradable polymers scrutinize supplier practices more than ever; documentation on byproduct handling and carbon capture systems now outweighs small price differences. We’ve seen increasing requests for certificates beyond purity, such as residual solvent profiles and heavy metal screenings. Our team shares real-life, not canned, responses about how each sample was manufactured.

    Summary of Value Compared with Alternative Intermediates

    For researchers and manufacturers looking for reliability, flexibility in reactivity, and easier compliance, our 1-(Methylsulfonyl)-4-Nitrobenzene brings notable advantages. The balance of stability and activity supports advanced, multi-step synthesis without demanding overly restrictive conditions or specialty storage. Experience has shown that small details—like tight drum closures, real-time analytical data, and close batch monitoring—pay the greatest dividends when chemists handle hundreds of kilograms per year.

    Alternative nitroaromatic intermediates may offer lower costs or legacy familiarity, but the methylsulfonyl derivative stands apart for ease of downstream substitution and generally less complicated waste handling. Less odor and dust mean safer, more hygienic working environments for crews operating scales from a few grams up to reactors handling hundreds of liters. In our view, working with this compound equates to fewer unexpected surprises at scale.

    Looking Ahead: Shifting Production with Industry Needs

    Advances in elemental analysis, continuous manufacturing, and digital tracking have changed how we approach every intermediate, including 1-(Methylsulfonyl)-4-Nitrobenzene. Our operations have adjusted to these shifts, integrating more digital monitoring for every process and investing in worker training focused on proactive issue identification. The results show in customer satisfaction and repeat orders, but also in the reduced disruption on our own floor.

    We know that our product’s value comes not only from its chemical uniqueness but from the reliability and transparency we provide. Each lot carries a history: hands that prepared it, watches that followed reaction curves, eyes that checked crystals. For every research or industrial project, consistent performance and trust in your supplier make all the difference—as real-world chemistry always has and always will.