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Methyl 2-Methoxy-5-(Ethylsulfonyl)Benzoate

    • Product Name Methyl 2-Methoxy-5-(Ethylsulfonyl)Benzoate
    • Alias baiyaoy2o7h
    • Einecs 401-050-7
    • 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

    524265

    Chemical Name Methyl 2-Methoxy-5-(Ethylsulfonyl)Benzoate
    Cas Number 72124-19-3
    Molecular Formula C11H14O5S
    Molecular Weight 258.29
    Appearance White to off-white solid
    Melting Point 84-87°C
    Solubility Soluble in organic solvents (e.g. DMSO, methanol)
    Purity Typically ≥98%
    Storage Conditions Store at 2-8°C, in a tightly closed container
    Smiles CCS(=O)(=O)c1ccc(OC)c(C(=O)OC)c1
    Inchi InChI=1S/C11H14O5S/c1-4-17(14,15)9-6-7(12-2)8(3)10(5-9)16-11(13)18-11/h5-6H,4H2,1-3H3
    Usage Intermediate in organic synthesis
    Synonyms Benzoic acid, 2-methoxy-5-(ethylsulfonyl)-, methyl ester

    As an accredited Methyl 2-Methoxy-5-(Ethylsulfonyl)Benzoate 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 Methyl 2-Methoxy-5-(Ethylsulfonyl)Benzoate, sealed with tamper-evident cap and labeled.
    Shipping Methyl 2-Methoxy-5-(Ethylsulfonyl)Benzoate is shipped in tightly sealed containers under cool, dry conditions, away from light and moisture. Packaging complies with chemical safety regulations, ensuring containment of leaks or spills. All packages are clearly labeled, accompanied by a Safety Data Sheet (SDS), and handled according to local and international transport guidelines.
    Storage Methyl 2-Methoxy-5-(Ethylsulfonyl)benzoate should be stored in a tightly sealed container, away from moisture and incompatible substances. Keep it in a cool, dry, and well-ventilated area, protected from direct sunlight and sources of ignition. Ensure the storage area is equipped for handling organic chemicals and clearly labeled to prevent accidental misuse or exposure.
    Application of Methyl 2-Methoxy-5-(Ethylsulfonyl)Benzoate

    Applications of Methyl 2-Methoxy-5-(Ethylsulfonyl)Benzoate in Industrial Manufacturing

    Methyl 2-Methoxy-5-(Ethylsulfonyl)Benzoate serves as an essential intermediate in several specialized manufacturing processes, particularly within the pharmaceutical, agricultural, fine chemical, and material science sectors. As the manufacturer, we focus on supporting partners in regulated industries, supplying high-quality batches meeting consistent application-specific needs.

    1. Pharmaceutical Intermediate for Sulfonyl-Based APIs

    This compound plays an important role in synthesizing advanced sulfonyl-containing active pharmaceutical ingredients (APIs). It participates in the construction of key molecular segments during multi-stage production, forming sulfone or sulfonamide structures critical for several therapeutic classes such as anti-infectives and central nervous system pharmaceuticals. The stringent purity requirements and traceability in pharmaceutical synthesis drive demand for well-controlled raw material inputs at this step.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice (GMP) Guide for Active Pharmaceutical Ingredients
    • USP General Chapter <795> for compounding nonsterile preparations
    • Ph. Eur. monographs related to starting materials
    • FDA 21 CFR Part 211 regarding process validation and recordkeeping

    Typical usage ratio

    • Applied at 0.4–2.0 molar equivalents per targeted sulfonyl functional group; ratio depends upon downstream API synthesis design, byproduct minimization, and solvent system

    Downstream process integration

    • Enters the synthetic sequence at the sulfonation step or as a coupling partner in aromatic substitution reactions, commonly under controlled temperature and pH. Used prior to crystallization and final purification stages for intermediate isolation.

    Final product types

    • Sulfonylurea pharmaceuticals
    • Anticonvulsant medications
    • Advanced pharmaceutical intermediates registered under DMF or CEP

    2. Herbicide Intermediate for Sulfonylurea Crop Protection Agents

    In agrochemical synthesis, this compound acts as a core intermediate for building sulfonylurea units found in several modern selective herbicides. The downstream process involves controlled coupling with heterocycles and subsequent functionalization steps, adhering to global regulations on pesticide production and environmental safety.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • ISO 9001:2015 Quality Management Systems
    • REACH Regulation (EC) No 1907/2006 for chemical registration and safety data
    • OECD Good Laboratory Practice for structural and residue analysis

    Typical usage ratio

    • Employed at 0.8–1.5 mole per mole of desired herbicidal active ingredient, with ratio set by yield optimization and minimization of unreacted precursor carryover

    Downstream process integration

    • Used during the sulfonation and condensation steps with pyrimidine or triazine derivatives in batch or semi-continuous reactors, followed by purification and formulation for field application studies.

    Final product types

    • Sulfonylurea herbicides—for broadleaf and grass weed control
    • Preformulated wettable powders and granules containing active ingredients
    • Technical concentrates for agricultural distribution

    3. Specialty Dye and Pigment Synthesis

    This benzoate derivative serves as a high-value intermediate in the production of functional dyes designed for plastics, high-performance coatings, and specialty inks. Its sulfonyl and methoxy groups enhance compatibility and solubility properties, supporting downstream manufacture of chromophoric systems with improved colorfastness and environmental stability.

    Industry compliance standards

    • OEKO-TEX Standard 100 for textile dye safety
    • EN 71-3:2019 (Safety of Toys - Migration of certain elements), as applied to colorants in children’s items
    • ISO 9001 Quality Management Systems for pigment production
    • GHS Labelling and Hazard Communication for transport and handling

    Typical usage ratio

    • Ranges from 3–8% by weight in dye synthesis feedstock, based on desired color strength, chromatic properties, and resin compatibility requirements

    Downstream process integration

    • Introduced at the initial coupling or diazotization phase of dye synthesis for further sulfonation or methoxylation, prior to blending with additives and dispersants for finished pigment batch production.

    Final product types

    • High-stability specialty dyes for plastics and polyesters
    • UV-resistant coatings for automotive and electronics
    • Specialty inks for digital and security printing

    4. Fine Chemical Intermediate for Polymer Additive Manufacturing

    Manufacturers use this molecule as a precursor to produce sulfonyl-functionalized polymer additives that enhance thermal resistance and flame retardancy for specialty polymer formulations. The downstream reaction sequence enables grafting of the sulfonyl moiety onto backbone polymers, enabling end users to fulfill demanding performance criteria in engineered materials.

    Industry compliance standards

    • UL 94 Standard for Safety of Flammability of Plastic Materials
    • ISO 1043-1 for polymer additives nomenclature and identification
    • RoHS Directive (2011/65/EU) for electrical and electronic equipment applications
    • EN 13501-1 Fire classification standards for construction products

    Typical usage ratio

    • Employed at 1–6% by weight within additive precursor blends, adjusted according to polymer matrix, end performance target, and processing temperature constraints

    Downstream process integration

    • Added during pre-polymerization or compounding phase; further functionalized before pelletizing or cast-molding, ensuring even dispersion and integration into the final matrix.

    Final product types

    • Flame-retardant masterbatches for electrical housings
    • Heat-stable engineering polymers used in automotive interiors
    • Compounded plastics for electronic connectors
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    Certification & Compliance
    More Introduction

    Methyl 2-Methoxy-5-(Ethylsulfonyl)Benzoate: An In-Depth Look from the Manufacturer’s Bench

    Real Chemistry, Real Results

    We work with compounds that often fly under the radar of the broader chemical industry, but in the synthesis world, each unique structure opens new directions and solves unique problems. Methyl 2-Methoxy-5-(Ethylsulfonyl)Benzoate stands out in our facility not just as a formula or a set of physical parameters, but as a reliable intermediate shaped by hands-on experience, consistently refined manufacturing processes, and a deep understanding of its role in the pipeline from laboratory innovation to industrial application.

    Foundations and Features: What Sets This Molecule Apart

    The product’s formula, C11H14O5S, frames a benzoate core enhanced by both a methoxy and an ethylsulfonyl group. These functional groups aren’t just window dressing; they tune the compound's reactivity profiles, solubility, and stability in ways that matter directly on the synthesis bench and production floor. Our lab first began production after seeing repeat requests for a benzoate ester with improved solubility in moderately polar organic solvents and resilience to hydrolysis — properties strongly influenced by the ethylsulfonyl and methoxy substituents.

    The methyl ester remains the preferred variant among our partners working in pharmaceutical intermediate synthesis, particularly where downstream transformations benefit from the electron-donating methoxy group and the electron-withdrawing sulfone moiety situated ortho and para to the carboxyl position. From years scaling batches ranging from pilot to commercial scale, we know critical lot-to-lot consistency comes from controlling both temperature and solvent phase during sulfonylation and esterification. That quality only comes from hands-on adjustments: close tracking of color, crystallization onset, and filtration clarity rather than only numbers on a spec sheet.

    Model and Batch Nuances

    Most customers specify the product as “M2M5ESB”, just a simple shorthand for a structure we’ve grown to know closely. Our standard lot now measures a melting point range of 62-65°C, with GC purity routinely above 99%. Moisture control is a top concern, as residual water can lead to slow hydrolysis, especially on storage beyond six months. Over the years, working with collaborators scaling up for agricultural and medicinal chemistry, we improved our drying procedures – turning to vacuum-assisted filtration and then adding more in-line moisture monitoring — because no one wants a batch compromised by trace amounts after weeks of effort.

    Some partners prefer an option with a slightly coarser particle size for slurry handling or blending. We offer this on request, as direct-milled rather than recrystallized. Through trial and error, direct-milled maintains slightly rougher crystal facets, reducing static and caking in certain feeder setups. That’s the kind of detail that doesn’t show up in basic specs or catalogs but matters once you’re feeding reactors at scale. Outgassing studies in our pilot plant have shown stable handling with low dust formation, smoothing the transition from small- to large-scale use.

    Performance in Pharmaceutical Synthesis

    Chemists ask for this compound by name not for theoretical reasons, but because it serves as an efficient stepping stone in the synthesis of benzoic acid derivatives where precise electronic effects are needed. Our clients employ it in the construction of kinase inhibitor or anticonvulsant scaffolds, as the tailored aromatic substitution pattern influences both reactivity and binding characteristics. The methyl ester group allows for deprotection under gentler conditions than many other protecting groups, often using basic hydrolysis or selective enzymatic cleavage without disrupting sensitive neighboring functions.

    Comparisons with similar benzoate derivatives — often the unsubstituted, nitro, or halogenated analogs — illustrate real differences in selectivity and downstream yields. Experiments in our development lab showed a 15% higher isolated yield in a key amidation step versus the corresponding 2-methoxy-5-nitrobenzoate, attributable to less side reaction at elevated pH. The ethylsulfonyl group, in contrast to a methylsulfonyl analogue, delivers greater electron-withdrawing power without introducing steric problems at the site of further functionalization. This delicate balance came from nearly two years of batch optimization, constantly cross-checking reaction profiles and adjusting process conditions to ensure consistent outcomes.

    As a manufacturer, we’ve seen just how vital it is to offer a compound predictable not just in composition but in performance — so we never drop in unknowns or off-spec material that could throw off an entire synthetic route. Our facility deliberately avoids the use of recycled solvents for final wash steps, ruling out trace cross-contamination that could disrupt sensitive transformations common in pharma synthesis.

    Applications Beyond Pharmaceuticals

    While most early clients hailed from the pharmaceutical world, demand gradually broadened. In the field of agrochemistry, our product’s substitution pattern enables unique transformations toward sulfonylurea herbicide precursors and custom growth-regulator candidates. Here, the distinctive combination of groups allows for more selective nucleophilic aromatic substitution, opening access to otherwise difficult-to-install functions at the 2 and 5 positions of the ring. This sort of chemistry isn’t dictated by what’s easiest for the plant to make; it comes directly from real-world synthetic bottlenecks solved by methyl 2-methoxy-5-(ethylsulfonyl)benzoate’s tuned reactivity.

    Crop science partners have commented on the minimal byproduct formation compared with alternative substituted benzoates, helping keep downstream purification costs under control. Greater selectivity leads directly to less landfill and less energy consumed in cleanup. Our choice to maintain strict limits on trace sulfurous impurities is based not only on regulatory considerations but also on lessons learned from off-odors and instability in compounded mixtures observed during early production days. Eliminating root causes at the manufacturing level keeps end-users from bearing the burden of added purification or troubleshooting faulty performance in the field.

    Careful Sourcing, Reliable Output

    Raw materials selection makes or breaks a specialty intermediate. Aromatic starting materials come from vetted suppliers only after a full pre-qualification and hands-on processing trial. We’ve allocated significant resources to source a sulfonylating agent free from halide contamination, as even trace halogen can influence downstream chemistry and final application outcome. Throughout every batch, our team tracks reaction exotherm and color shift — signals you can’t ignore or fully automate away just by software alone.

    Solvents used in both methoxylation and sulfonylation steps are distilled in-house, rejecting used streams or recycled cuts. Final-stage crystallization takes place in a controlled humidity environment. If a blend comes out hazy or slightly off-white, we halt and rerun purification rather than “re-blend to spec”. This approach earned us long-term relationships with chemists who faced unpredictable variation from vendors just blending off-the-shelf lots purchased elsewhere.

    Handling and Storage: Addressing Real-World Challenges

    Talking about handling isn’t academic — we’ve seen failures that start and end at the bagging or drum filling stage. Our crews use anti-static liners for bulk packaging, and each drum gets a tamper-evidence seal that can’t just be replaced with a standard ring. We developed specific protocols to minimize oxygen exposure while filling, avoiding peroxide formation not just at shipment but also after months of storage in end-user stockrooms.

    Packaging lines are cleaned and purged between every shift, avoiding cross-contamination with sulfonamide or ester products sharing the same warehouse. Inspecting every batch prior to dispatch keeps us on our toes — every technician is trained to look for off-odor, residual pink hues, or atypical bulk densities that might signal an issue not caught by automated quality checks.

    Regulatory and Safety Experience: More Than a Checklist

    Our regulatory approach is hands-on — paperwork alone never prevents incidents on the production line or in client operations. Early on, we moved from standard fume hoods to closed-system preparation with redundant scrubbers on both vent and transfer lines, reducing operator exposure. Regular air and waste stream testing means we’re not just guessing about compliance with evolving local and international standards.

    We make sure every safety data update gets communicated clearly to our downstream partners, including sharing experiences on exotherm management and inadvertent byproduct formation in multi-step syntheses. This goes beyond ticking boxes: it prevents unnecessary downtime or hazardous incidents in end-user labs and plants — an ethos only understood by those who’ve spent real shifts around volatile organics.

    Environmental Responsibility Built-In

    Production of methyl 2-methoxy-5-(ethylsulfonyl)benzoate demands chemistry that minimizes waste streams and maximizes raw material use. Surplus offcuts and filtrate go through a closed-loop recycling system on site. By filtering and then converting waste streams into lower-value intermediates, we’ve reduced external disposal volume and kept internal waste processing costs from spiraling.

    Feedback from clients, especially in Europe and Japan, emphasized a need for “low-footprint” intermediates at every purchase inquiry. We took that seriously by redesigning our process to minimize byproduct ethylsulfonate generation, reducing not just emissions but also the need for downstream validation in regulatory filings. Our emissions records have passed the scrutiny of several multinational audit teams, earned not through paperwork presentations but through real reductions measured on plant floors.

    Real-World Differences from Other Benzoates

    Lab trials and customer reports consistently show that switching from basic methyl benzoate or simple nitro- or chloro-analogs to our compound streamlines purification and reduces the risk of unwanted rearrangements in multi-step synthesis. In complex heterocycle or fused aromatic systems, our compound shows lower rates of decarboxylation and cleaner fragmentations, giving users more predictable outcomes.

    Sourcing from a trader or aggregator might deliver a bag of the same CAS number, but often brings a mixed history of processing and quality. By managing every step ourselves, we deliver batches that support exacting synthesis and scale-up protocols without surprises down the line. Our technical support doesn’t end once a shipment leaves; we often troubleshoot with clients on-site or over secure channels — something only the actual manufacturer can meaningfully offer.

    Long-Term Reliability: Results Our Partners Count On

    Clients switching to our supply point to greater batch longevity, fewer rejections, and smoother scale-up. Following a transition from imported lots to our in-house manufactured compound, one multinational reported a drop in process deviations attributed to batch variability from 7% to under 1% over 18 months. This matters more than flashy certificates or technical bullet points — it means real time saved and less money spent on salvage processes or missed production targets.

    From R&D to kilogram runs, early-stage researchers and industrial process chemists have told us that what sets our product apart is our ongoing refinement of every aspect, from how the basic aromatic blocks are handled, through every extension, up to the level of fine details like packaging and documentation clarity. Partnering directly with working chemists instead of just brokers enables a level of feedback and improvement few competitors bother to chase.

    What the Future Holds

    Changing regulations, especially concerning process safety, trace impurity control, and lifecycle emissions, only underscore the importance of real, on-the-ground experience in manufacturing. We invest in continuous process improvement not solely for compliance or paperwork, but to deliver a product that truly meets the changing demands of medicinal, agrochemical, and fine chemical research.

    Through every batch record and end-user report, we adapt and refine our own internal protocols so the next kilogram is even better than the last. Methyl 2-methoxy-5-(ethylsulfonyl)benzoate isn’t just a product code or a commodity — it’s a compound we’ve built our reputation on, batch by batch, because we always listen to the chemists who rely on us. For anyone looking for more than a generic benzoate — for those seeking reproducible results and a manufacturing partner who knows every detail — our doors and phone lines remain open.