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3-(Methylsulfonyl)Benzoic Acid

    • Product Name 3-(Methylsulfonyl)Benzoic Acid
    • Alias NSC 407292
    • Einecs 416-520-7
    • 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

    616020

    Chemical Name 3-(Methylsulfonyl)benzoic acid
    Molecular Formula C8H8O4S
    Molar Mass 200.21 g/mol
    Cas Number 17668-76-9
    Appearance White to off-white crystalline powder
    Melting Point 166-170 °C
    Solubility Slightly soluble in water, soluble in organic solvents
    Boiling Point Decomposes before boiling
    Smiles CCS(=O)(=O)C1=CC=CC(=C1)C(=O)O
    Pubchem Cid 26124
    Synonyms meta-(Methylsulfonyl)benzoic acid, m-(Methylsulfonyl)benzoic acid

    As an accredited 3-(Methylsulfonyl)Benzoic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing White HDPE bottle labeled “3-(Methylsulfonyl)Benzoic Acid, 25 grams,” sealed with tamper-evident cap; hazard and storage instructions printed.
    Shipping 3-(Methylsulfonyl)benzoic acid is shipped in tightly sealed, chemical-resistant containers to prevent contamination and moisture ingress. Packaging complies with relevant regulations for safe transport of chemicals. The product is clearly labeled with hazard warnings and requires storage in a cool, dry location, protected from direct sunlight and incompatible substances during transit.
    Storage 3-(Methylsulfonyl)benzoic acid should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from sources of heat and incompatible materials such as strong acids, bases, and oxidizers. Protect from moisture and direct sunlight. Store at room temperature, and ensure proper labelling to prevent accidental misuse. Follow all relevant safety guidelines when handling and storing.
    Application of 3-(Methylsulfonyl)Benzoic Acid

    Applications of 3-(Methylsulfonyl)Benzoic Acid in Industrial Manufacturing

    As a direct manufacturer of 3-(Methylsulfonyl)Benzoic Acid with extensive quality control capacity, we supply this specialty intermediate for a targeted range of advanced production sectors. Our material is manufactured, tested, and qualified to meet the nuanced requirements of each downstream process highlighted below.

    1. Pharmaceutical Intermediate for Nonsteroidal Anti-Inflammatory Drug (NSAID) Synthesis

    We supply 3-(Methylsulfonyl)Benzoic Acid directly to pharmaceutical manufacturers as a selective intermediate in the multi-step synthesis of specific NSAID actives. The compound contributes the sulfonyl functional group required in molecular modification processes during the diversification of arylacetic acid derivatives. The material consistently meets the purity and impurity profile specifications critical for API precursor manufacture, supporting process efficiency and yield in high-volume batch operations.

    Industry compliance standards

    • ICH Q7: Good Manufacturing Practice (GMP) for Active Pharmaceutical Ingredients
    • USP General Chapter <1078>, EudraLex Volume 4 Part II
    • 21 CFR Part 211 (Current Good Manufacturing Practice for Finished Pharmaceuticals)
    • Ph. Eur. monograph requirements for relevant NSAIDs

    Typical usage ratio

    • 0.8–1.2 molar equivalents, calculated based on target NSAID batch scale and route selectivity; adjusted for byproduct minimization

    Downstream process integration

    • Integrated during arylation and sulfonylation steps, prior to final API crystallization
    • Charged into jacketed reactors during initial condensation and subsequent reflux with coupling agents

    Final product types

    • Bulk NSAID active pharmaceutical ingredients (e.g., etofenamate derivatives)
    • Validated API intermediates compliant for onward contract manufacture

    2. Agrochemical Synthesis Route for Selective Herbicides

    Manufacturers in the agrochemical sector utilize this molecule as a structural building block for the development of methylsulfonyl-substituted benzoic herbicides. Its unique electronic properties facilitate regioselective modifications that are necessary during the production of sulfonamide-type pre-emergent herbicides, improving both potency and crop safety profiles under field conditions.

    Industry compliance standards

    • FAO/WHO Specification for Plant Protection Products (FAO/WHO–JMPS)
    • ISO 9001:2015 Quality Management for pesticide intermediates
    • Chinese National Standard GB 2763 for agricultural chemical residues
    • European Regulation (EC) No 1107/2009 (authorization of plant protection products)

    Typical usage ratio

    • 1.5–2.0 weight % in total coupling mixture, optimized for desired sulfonyl group content in multi-step synthesis

    Downstream process integration

    • Introduced after primary aromatic ring construction, frequently following halogenation or amidation
    • Blended with amine or triazine reactants in a solvent, then carried forward to purification

    Final product types

    • Methylsulfonylbenzoic acid-based herbicide active substances
    • Formulated herbicide concentrate products for cereals and row crops

    3. Monomer for Advanced Polyimide Materials

    Producers of high-performance polymers employ this substance as a comonomer in polyimide resin synthesis. The sulfonyl functional group enhances dielectric, thermal, and flame-retardant attributes of the resulting polymer matrix, making the additive invaluable for specialist polyimide films and molded components in the electronics and aerospace fields. Our material is produced with strict particle size and metal contamination controls to enable direct scale-up to commercial extrusion and lamination lines.

    Industry compliance standards

    • UL 94 flame classification for plastics
    • RoHS Directive (2011/65/EU) for electronic component safety
    • IEC 61249-2-21 (Halogen-free requirements for electronic circuit boards)
    • FDA 21 CFR 177.2440 (Polymers, for indirect food contact applications, as applicable)

    Typical usage ratio

    • 3–10 mol% relative to dianhydride monomer component; formulation set-point selected based on targeted thermal and electrical performance

    Downstream process integration

    • Fed into polycondensation reactors along with aromatic diamines and dianhydrides
    • Dissolved in NMP or DMF solvent for homogeneous mixing prior to imidization step

    Final product types

    • Flexible polyimide films for high-frequency circuitry
    • Thermoset polyimide laminates for aerospace and automotive electronics

    4. Precursor for Specialty Dyes and Optical Whitening Agents

    In dye manufacturing, formulators use 3-(Methylsulfonyl)Benzoic Acid as a precursor for sulfonyl-aryl synthetic dyes exhibiting enhanced aqueous solubility and colorfastness. The material fits established procedures for producing specific classes of azo and stilbene-based optical brighteners, crucial for high-grade textile and paper processing. Consistent batch-to-batch hue performance, driven by purity controls, allows reliable color formulation adjustments in downstream blending and finishing stages.

    Industry compliance standards

    • OEKO-TEX Standard 100 (restricted substance list for textile auxillaries)
    • ZDHC MRSL (Zero Discharge of Hazardous Chemicals Manufacturing Restricted Substances List)
    • EU REACH Regulation (EC) No 1907/2006 (dye registration and safety data)
    • GB/T 7573 for color fastness in textiles

    Typical usage ratio

    • 2–5 mol% in coupling reaction stage, increased for higher-intensity color targets; finetuned based on shade reproducibility and byproduct yield

    Downstream process integration

    • Charged with amine or diazonium salts in diazotization or coupling reactors
    • Solubilized before acidification and salt isolation stages in the dye synthesis workflow

    Final product types

    • Water-soluble synthetic dyes for polyester, cotton, or paper
    • Optical whitening agents for industrial laundry or paper pulping processes

    5. Fine Chemical Intermediate in Custom Organic Synthesis

    Experienced contract and specialty chemical manufacturers use this acid as an intermediate for assembling complex, functionalized aromatic compounds. Its methylsulfonyl group provides an electron-withdrawing site that enables regioselective nucleophilic substitution and facilitates downstream transformations like Suzuki couplings or Friedel–Crafts acylations in multi-ton custom synthesis campaigns. We guarantee analytical support and impurity mapping to meet the high repeatability needs of kilo-lab to commercial scale-up settings.

    Industry compliance standards

    • ISO 9001:2015 and ISO 14001:2015 (quality and environmental for specialty chemicals)
    • Chemical Facility Anti-Terrorism Standards (CFATS; US DHS, for critical chemistries)
    • Custom specifications dependent on client project, regularly includes LC-MS/GC-MS impurity profiling

    Typical usage ratio

    • Varies by target molecule and synthesis sequence; typically 1.0 equivalent in the electrophilic aromatic substitution phase

    Downstream process integration

    • Loaded for direct functionalization in aromatic substitution, then advanced to cross-coupling or cyclization as specified in the process route
    • Handled under inert atmosphere when moisture-sensitive downstream reagents require protection

    Final product types

    • Specialty aromatic intermediates for pharmaceuticals or performance chemicals
    • Building blocks for discovery chemistry or pilot-scale synthesis projects
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    Certification & Compliance
    More Introduction

    Introducing 3-(Methylsulfonyl)Benzoic Acid: A Reflection from the Factory Floor

    Everyday Chemistry and Honest Production

    Stepping into our facility each morning, the faint, familiar scent of solvents and reactors humming at their rhythm tells me another day’s work will shape tools for chemists, researchers, and process engineers far beyond these factory walls. Among the compounds filling our drums stands 3-(Methylsulfonyl)benzoic acid—a molecule built for the pace and pressure of modern synthesis. We have learned through hands-on production what this compound can achieve and what sets it apart from similar benzoic acid derivatives.

    A Closer Look at the Product

    Our 3-(Methylsulfonyl)benzoic acid, produced batch after batch in stainless reactors and purified across several crystallizations, shows up as an off-white to pale cream crystalline solid. The typical batch comes in at a minimum 99% purity based on HPLC analysis. Over years of growing production, we have leaned heavily into tight control on both the methylsulfonyl substitution and the aromatic positioning. A misplaced functional group here drops process yields later by double digits or clogs research pipelines for weeks.

    We standardize our particle size because too coarse and filtration slows down in downstream processing, while too fine and the dust becomes a headache for formulation and handling. Moisture content runs low to avoid caking or hydrolysis. The molecular formula, C8H8O4S, leads to a molecular weight of 200.21 g/mol—something that rarely means much until a customer runs a reaction scale-up and sees how the numbers align with their feedstock calculations.

    Why We Make This Compound

    Decades back, most benzoic acid derivatives came from smaller local plants, sometimes by hand and often with inconsistent profiles. Now, many laboratories expect intermediates like 3-(Methylsulfonyl)benzoic acid with both a clean chemical fingerprint and batch-to-batch reproducibility. The methylsulfonyl group, with its balance of electron withdrawing strength and metabolic stability, turns this acid into a reliable anchor for more advanced synthesis:

    These applications rarely show up on glossy brochures. The actual work involves centrifuge tanks, precise thermal control, and plenty of cross-checking—each step ensuring the intermediate behaves as expected in the next reaction vessel.

    Not All Benzoic Acids Are Alike

    On the surface, the methylsulfonyl on the three position looks like a minor twist compared to, say, 4-methylsulfonylbenzoic acid or the plain benzoic acid itself. We have run side-by-side crystallizations and spot-checked reactivity for over a decade. The position and nature of the sulfonyl group matter and they show up during actual workups. Electrophilic substitution reacts distinctly compared to the unmodified acid, and the three position allows for cleaner substitution at the ortho or para sites, depending on your next steps.

    The methylsulfonyl group soaks up electron density more strongly than a plain methyl or methoxy, making the compound behave differently under both acidic and basic reaction conditions. This opens up some regioselective chemistry that simply doesn’t work with unsubstituted or 4-methylsulfonyl analogs. Some customers notice this difference when troubleshooting stalled reactions and, after hearing from our technical service, turn back to our compound. Rarely do they switch back.

    We routinely see 3-(methylsulfonyl)benzoic acid selected in place of sulfonic acids, especially where solubility or downstream process compatibility matter. Comparisons with 3-(methylthio)benzoic acid always spark debate among chemists—sulfoxide or sulfone, leaving group stability or electron withdrawal, ease of oxidation or reduction. Most of our long-term users agree the sulfone gives both stability and reactivity windows that hit the sweet spot for diverse synthetic planning.

    Lessons Learned: Process, Quality, and Responsibility

    Producing high-purity aromatic acids long ago stopped being just about following reaction recipes. Over the years, we have weathered challenges in scale-up, purity optimization, and regulatory requirements. Our technical team, working beside operations, moved from small glassware to industrial vessels and learned a good deal from each step.

    We saw early on that byproducts build up quickly if the reaction temperature profile drifts or if condensation isn’t monitored closely. On more than one occasion, trying to speed up the process led to side-reactions that dropped final purity by several points. Customers notice changes as subtle as slight yellowing in a batch, often reporting corresponding shifts in their downstream application yields.

    Moisture pick-up sometimes taints the acid during long-term storage or shipping. We shifted to better liners and rapid, on-line drying to limit this, but it called for new SOPs and retrained staff. Storage conditions in our warehouses match or exceed GSP guidelines because preserving batch quality isn’t just a matter of keeping up appearances—it reflects real changes in analytical profiles and safety for users.

    Quality assurance means more than ticking boxes for standard batch tests. Our QC specialists run repeated HPLC and NMR checks, but we value feedback from researchers and process chemists using our acid in live projects. Several times, fine feedback led us to tweak processing temperatures or extend purification runs, resulting in more reproducible syntheses for both us and our partners.

    Value Differences—The View from Production

    Most requests for this acid start with purity specs or cost discussions. Over time, what keeps partners coming back is the certainty that every drum shipped matches their last successful project. Some academic groups care most about analytical purity for isolating minor reaction products. Process chemists at larger companies need batch availability and consistency over many months.

    We invest in process validation and traceable lot records. Several years ago, a multinational partner flagged an outlier result traced to a supplier’s change in solvent source. We rebuilt our audit system to track and record not just solvents but also cleaning regimes and operator training cycles. The audit trail lets us go back and pinpoint where even minor variations slip in—and fix them quickly.

    Custom requests sometimes surprise us: particle size fractionation, alternate crystal forms, or micronization for specific formulations. While these features raise costs and slow output, we recognize that some research needs demand extra steps. Meeting those requirements draws us closer to our partners. Each variant starts with a discussion, samples, and detailed analytical comparisons, since we know that the knock-on effects always reach further than anyone expects.

    Practical Use and Technical Support

    3-(Methylsulfonyl)benzoic acid might seem like a niche intermediate, but its reliable reaction profile and process stability encourage a wider range of experiments. We encourage technical consultations before scale-up, since bench chemistry sometimes tricks even experienced researchers. On occasion, poorly dried acid has caused slow reaction kinetics or batch failures. Our support team often provides guidance on recommended solvents, solution handling, and optimal reaction conditions based on our own in-house tests.

    We learned, through experience, that direct handling of the powder calls for standard PPE and dust containment. Small spills should be collected dry, since the sulfone group resists rapid hydrolysis, but introducing unnecessary moisture is best avoided. Waste handling follows the expected regulatory path for aromatic acids and sulfones—which we follow to the letter, having seen penalties outpace any short-term savings from shortcuts.

    We manufacture with experienced chemists, not just operators moving levers. A meaningful portion of our staff cycle through different sections of the plant: synthesis, filtration, drying, and packing. This rotation sharpens instincts for what a good batch looks, smells, and feels like long before any analytical result confirms it. We know the signs of a healthy, productive batch from a glance and a sniff, catching issues early to avoid downstream disappointment.

    Differences from Others: Details that Shape Real Outcomes

    It might be tempting to treat benzoic acid derivatives as interchangeable, distinguished only by paperwork or catalog descriptions. Our day-to-day draws a clearer line. The three-position methylsulfonyl stands apart from four-position analogs by its core electronic character—pulling electron density with enough force to shift reactivity trends but sparing enough to allow downstream substitutions. Our direct production offers a tailored control over particle size, purity, and substitution pattern—avoiding broad blend lots and instead dedicating each run to a clearly specified output.

    Customers sometimes ask about blending or reprocessing batches to salvage subpar intermediates, but our experience discourages this. Adding inconsistency or minor impurity profiles often complicates downstream chemistry in unpredictable ways. Rather than merge batches, we choose to adjust process controls and ensure every output can serve as a repeatable building block. Down the line, suppliers and researchers have thanked us for leaning toward tighter, more reliable output parameters.

    Sulfonic acid analogs may offer higher acidity, but their solubility and stability profiles often edge out key users who prefer clean, crystalline sulfones. Given the stringent quality requirements of regulated markets, our 3-(Methylsulfonyl)benzoic acid stays competitive because we keep documentation, process records, and testing open for inspection. Several customers with audit teams comment on our willingness to share detailed batch analytics and process change histories.

    Market Shifts and Evolving Demands

    Global sourcing of fine chemicals changes with cost pressures, environmental regulations, and supply chain disruptions. We have weathered periods when raw material pricing spikes caused by trade disputes threatened steady supply. In those times, keeping robust secondary supplier relationships and a transparent inventory protocol let us honor long-term contracts without shorting quality or production scale. While price matters, reliability often determines ongoing business.

    Sustainability is moving from a talking point to a daily responsibility. We invested in closed-system reactors and updated waste neutralization lines to limit any emissions. Each improvement aimed to exceed local environmental compliance and cut energy costs—moves that tell a story both in community acceptance and long-term customer loyalty.

    The regulatory scene gets tougher every few years, as both national and international agencies tighten expectations on documentation, batch traceability, and environmental impact. We integrate these shifts rapidly and keep open channels with compliance teams, seeing the result not as a burden but as part of maintaining a role as a trusted supplier.

    Challenges and Future Solutions

    Producing specialty chemicals always invites unexpected hurdles. Whether a pump fails during a critical reaction phase or a batch is delayed at port clearance, we have learned to document and share these challenges transparently with customers. Mistakes, communicated quickly, tend to be forgiven when honest solutions follow close behind.

    Innovation happens at every step—sometimes in the labs, sometimes on the plant floor. Recent experiments in catalytic purification shaved hours off process time while reducing solvent use, an unplanned benefit born from a simple staff suggestion. We encouraged routine problem-reporting and innovative ideas through daily shift meetings and cross-departmental discussions.

    Flexible packaging solutions, like semi-bulk lined drums with moisture-resistant valves, cut down on product degradation in shipping to humid regions. Customized packing requests have grown steadily, and although this pressured our logistics team, it opened new markets not previously accessible.

    In the Lab, In the Plant: The Human Touch

    No matter the automation or digital monitoring, real improvement often begins as word of mouth. A seasoned technician spots a variation, flags it fast, and saves a batch before a small mistake grows into a costly recall. Each year we allocate part of our budget to staff training on both analytical tools and hands-on troubleshooting. Rewarding not just spotless output, but also open communication about near-misses, keeps our process honest and progressive.

    Face-to-face talks with customers—whether by video call or plant tour—get us closer to the concerns and ambitions that drive real chemical innovation. Most partnerships begin with a simple question or a tough troubleshooting dilemma. Over time, trust grows alongside shared understanding of what each product, batch, and chemical means for the downstream user.

    Conclusion: From Factory to Laboratory Bench

    Producing 3-(Methylsulfonyl)benzoic acid goes beyond following reaction equations or compiling purity certificates. It involves the kind of daily discipline, shared technical language, and hands-on care that bridges the gap between bulk chemicals and tailored research intermediates. Our experience, drawn from thousands of batches and countless customer questions, has shaped an approach that values predictability, process transparency, and a commitment to improving alongside new demands. Whether destined for pharmaceuticals, agrochemicals, or specialty materials, this benzoic acid derivative finds value in the connections, diligence, and pride of those who make it.