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Methyl Methanesulfonate

    • Product Name Methyl Methanesulfonate
    • Alias MMS
    • Einecs 214-684-5
    • 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

    933661

    Chemical Name Methyl Methanesulfonate
    Synonyms MMS, Methanesulfonic acid methyl ester
    Cas Number 66-27-3
    Molecular Formula C2H6O3S
    Molecular Weight 110.14 g/mol
    Appearance Clear, colorless to pale yellow liquid
    Boiling Point 156 °C
    Melting Point -32 °C
    Density 1.303 g/cm³ at 20 °C
    Solubility Miscible with water
    Flash Point 70 °C (closed cup)
    Odor Characteristic, irritating odor

    As an accredited Methyl Methanesulfonate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Brown glass bottle with secure cap, holding 100 mL of Methyl Methanesulfonate. Labeled with hazard symbols, chemical name, and CAS number.
    Shipping Methyl Methanesulfonate is shipped as a hazardous chemical under UN No. 3276. It should be packaged in tightly sealed containers, clearly labeled with hazard warnings, and transported in accordance with international and local regulations for toxic and flammable substances. Appropriate protective measures must be taken to avoid leaks and exposure during transit.
    Storage **Methyl Methanesulfonate** should be stored in a tightly closed container in a cool, dry, and well-ventilated area, away from incompatible materials such as strong oxidizers. Protect it from light and moisture. Store at room temperature and label appropriately, indicating its hazardous nature. Use secondary containment to prevent leaks or spills and restrict access to trained personnel only.
    Application of Methyl Methanesulfonate

    Applications of Methyl Methanesulfonate in Industrial Manufacturing

    As an experienced producer, we deliver high-purity Methyl Methanesulfonate (MMS) serving demanding industrial sectors. Our material supports multiple advanced applications, where process reliability, chemical precision, and regulatory compliance drive downstream production.

    1. Pharmaceutical Intermediate Synthesis

    Methyl Methanesulfonate finds direct use in medicinal chemistry as an alkylating reagent for synthesizing key active pharmaceutical ingredient (API) intermediates. Process chemists employ MMS for controlled methylation steps in the formation of methylated heterocycles, nucleosides, and small molecule scaffolds. Specific batch records stipulate traceability, and regulatory agencies pay close attention to genotoxic impurities, so our supply consistently meets stringent specs. During route design and scale-up, process development teams optimize the MMS input relative to substrate and solvent type, maintaining impurity limits and process safety during methyl group transfer.

    Industry compliance standards

    • ICH M7 guideline on genotoxic impurities (EMA/FDA/PMDA)
    • GMP Part II (EU EudraLex, 21 CFR 211 for API production)
    • USP <823> for radiopharmaceuticals (where used)
    • Ph. Eur. General Monographs for APIs

    Typical usage ratio

    • 0.9–1.5 molar equivalents per reactive site based on substrate limiting reactant
    • Adjusted for substrate reactivity and in situ generation protocols
    • Optimization to minimize excess in accordance with API impurity thresholds
    • Levels defined in individual process validation reports

    Downstream process integration

    • Added at controlled temperature in methylation reactors following pre-dissolution of substrates
    • Post-reaction, removed during aqueous workup or by solvent extraction, monitored by LC-MS for residues
    • Intermediate purification with crystallization or chromatography before downstream transformation
    • In larger sites, MMS charging via closed system per HSE guidelines

    Final product types

    • Methylated API intermediates (e.g., methylated purines, pyrimidines)
    • Custom pharmaceutical building blocks
    • Nucleoside analogues for antiviral drugs
    • Methylated fine chemicals destined for final API synthesis

    2. DNA Damage Reference Material for Genotoxicity Testing

    Genetic toxicology laboratories utilize our material as a positive control or standard damage agent in studies evaluating potential mutagenic or clastogenic effects of candidate pharmaceuticals, agrochemicals, or chemicals under OECD or GLP protocols. MMS induces defined DNA alkylation damage, so toxicologists calibrate their in vitro and in vivo assays using traceable, high-purity lots. Strict supply chain documentation and analytical profile ensure ready acceptance in regulatory submissions and proficiency tests.

    Industry compliance standards

    • OECD Test Guideline 471 (Bacterial Reverse Mutation Test)
    • OECD Test Guideline 476 (In Vitro Mammalian Cell Gene Mutation Test)
    • GLP (Good Laboratory Practice) compliance
    • ICH S2(R1) for genotoxic impurity assessment

    Typical usage ratio

    • Standard final concentrations of 1–10 μg/mL in liquid exposure medium
    • Set by protocol to produce reproducible, quantifiable DNA damage
    • Serial dilutions performed to establish concentration-response relationships
    • Adjusted per organism or cell line sensitivity

    Downstream process integration

    • Incorporated directly into culture medium or test solution prior to exposure phase
    • Serves as a control or to spike samples during positive control runs
    • Used to validate assay sensitivity and confirm batch acceptability
    • Residual MMS removed through washing steps post-exposure

    Final product types

    • Assay validation kits
    • GLP genetic toxicology study reports
    • Reference standards for laboratory QC
    • Regulatory dossier supporting documentation

    3. Specialty Synthesis in Agrochemical Development

    R&D centers and fine chemical manufacturers incorporate MMS as an alkylation component in synthesizing active agrochemical intermediates, particularly for sulfur- or nitrogen-containing heterocyclic scaffolds. Its selective reactivity supports late-stage functionalization steps. Regulatory-driven impurity control and traceability demand high batch consistency, and technical teams integrate our material in specific stage-gate manufacturing protocols for new herbicides or fungicides.

    Industry compliance standards

    • FAO/WHO Specification and Evaluation for Agricultural Pesticides
    • ISO 9001 certified quality management system for raw material traceability
    • EPA 40 CFR 158 (USA) for active ingredient synthesis
    • Good Laboratory Practice (GLP) for R&D batch studies

    Typical usage ratio

    • 1.0–1.3 equivalents relative to specific nucleophilic centers in heterocycle precursors
    • Dosed based on substrate solubility and required degree of substitution
    • Batch-to-batch adjustment according to raw material analytical profile
    • Monitored to ensure downstream product registration eligibility

    Downstream process integration

    • Fed sequentially in stirred tank reactors after primary condensation step
    • Solvent medium selected for compatibility and efficient phase separation
    • Work-up includes neutralization and separation, with attention to methylated by-products
    • QC releases material for subsequent formulation or further synthetic elaboration

    Final product types

    • Active agrochemical intermediates (herbicides, fungicides)
    • Sulfonated pesticide precursors
    • Specialty crop protection agents
    • Intermediates for plant growth regulators

    4. Analytical Reagent for Laboratory Research

    Chemical and bioscience laboratories source MMS as a specialty reagent for chemical modification of biomolecules, nucleic acid derivatization, and controlled alkylation in analytical method development. The extremely reactive methylating ability enables biochemists to probe DNA-protein interactions and study methylation patterns under precisely controlled conditions. Laboratories specify our analytical grade with COA and stability data to ensure result reproducibility in peer-reviewed research.

    Industry compliance standards

    • ISO/IEC 17025 for analytical laboratory accreditation
    • Internal laboratory quality standards for reagent traceability
    • IUPAC guidelines for reporting and use in publications
    • Institutional laboratory chemical hygiene protocols

    Typical usage ratio

    • 10–500 μM in nucleic acid alkylation assays
    • Concentration tailored to target substrate reactivity and method sensitivity
    • Volumes determined by reaction scale, typically 0.1–10 mL per experiment
    • Adjusted by protocol for enzyme inhibition or chemical DNA footprinting

    Downstream process integration

    • Added directly to DNA, RNA, or protein samples in buffered solutions
    • Reaction monitored by UV/Vis absorbance or mass spectrometry for completion
    • Followed by quenching and purification steps before analysis
    • Residues tracked in final sample to avoid interference in downstream assays

    Final product types

    • Nucleic acid and protein adducts
    • Modified oligonucleotides for gene editing research
    • Analytical kits for DNA damage and repair studies
    • Peer-reviewed scientific publications based on alkylation data
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    Certification & Compliance
    More Introduction

    Methyl Methanesulfonate: Practical Knowledge from the Manufacturer’s Floor

    Direct Experience Manufacturing Methyl Methanesulfonate

    Out on the chemical plant floor, few products draw as much direct attention as Methyl Methanesulfonate (MMS). Our years spent synthesizing, purifying, and delivering this compound have shaped our approach in more ways than any outsider might realize. Working with MMS is a lesson in consistency and focus. Our plant trains everyone, from new junior operators to seasoned technicians, that you can’t cut corners with this compound. People who want to understand MMS need to see the entire journey: from the distillation columns to the analytical lab, not just the sample bottle that gets sent in a box.

    We produce MMS so often that its faint medicinal, sweet odor is a familiar part of daily life here. A batch begins with careful reagent selection—methanol of high purity and methanesulfonyl chloride, both stored with tight controls. Every reactor run is calibrated to avoid introducing trace water, since hydrolysis during production ruins the yield and lowers product quality. Operators document the exothermic reaction’s profile, keeping the temperature steady. When the reaction mix travels into the separation phase, our experience has taught us to monitor phase splits for unwanted side-products. The clarity of that interface tells us more than any simple test strip. Years of running this process make it second nature to avoid over-refluxing.

    After distillation, the product emerges as a colorless liquid. We pack it into coated steel drums or compatible PEHD carboys for shipment. At this point, MMS has a purity above 99%, which our finished-goods QA lab confirms using high-performance liquid chromatography and NMR. Peaks on the chromatogram speak volumes: a sharp, uncompromising signal means quality production. The slightest shadow tells us it’s time to tweak process parameters.

    What Sets MMS Apart from Similar Chemicals

    There are manufacturers who talk about MMS and its relatives without sweating over their production differences. Our daily routines bring out the distinctions clearly. MMS is a superior methylating agent—fast-reacting, low volatility compared to alternatives like dimethyl sulfate, and with handling risks that reward careful respect without being unmanageable. Chemists in pharmaceuticals lean on MMS for gene mutation studies and alkylation reactions in research. Compared to ethyl methanesulfonate (EMS), MMS gives faster methyl transfer, though the smaller methyl group calls for extra care in controlling reaction selectivity.

    MMS works well in organic synthetics because it dissolves in both water and organic solvents. In the lab, that means less fuss with dissolving protocols and cleaner work-ups. Over time, our customers have confirmed that reactions run smoother and give cleaner products versus older methylating agents. What makes MMS even more practical is its byproduct profile: methanesulfonic acid, easily removed and detected. We track this carefully in our process stream, adding neutralization steps in waste-handling.

    Older alkylating agents, such as methyl iodide or methyl bromide, present a much higher toxicity burden and release halides into effluent. Our MMS avoids these legacy hazards. A crucial distinction lies in volatility. MMS remains liquid at room temperature and doesn’t volatilize aggressively, so dedicated fume extraction is still necessary, but you don’t face the runaway vapor pressure issues found with methyl halides. Plant operators tell us this fact alone improves safety, especially when scaling up for tens of kilograms in stirred tank reactors.

    Model and Batch History in Real-World Production

    We don’t market MMS under fanciful names—a batch is only as good as the certificate of analysis pinned to the drum. Every lot receives an internal code tied to raw material lots and reactor identification. Routinely, experienced operators track micro-scale pilot runs against full-scale campaigns, and we’ve found that seemingly minor tweaks in heating profiles create noticeable changes in color and GC area ratios.

    Most customers ask for lots in sizes ranging from 25 kg to bulk loads over 1,000 kg. Our technical staff has noticed that even a change in the order of addition will yield differences in stirring characteristics, especially in jacketed glass-lined vessels. Tuned process parameters—charge sequence, agitation speed, cooling rates—are written into our SOPs based on years of batch data collected on-site. Lab notes prove their value here: recording foaming, emulsions, or faint haze in the final product helps guide next runs. Actual users in the plant learn fast that trusting untested “internet protocols” is no substitute for hard-won process data.

    Why Methyl Methanesulfonate Matters to Industry

    Down in pharmaceutical synthesis, MMS serves as a fast and reliable methyl group donor, especially for nucleophilic substitutions on oxygen, nitrogen, or sulfur centers. Our production batches support some of the world’s top pharma labs, and we answer frequent technical queries every month about optimizing alkylation step yields. Academics and safety officers alike have called our plant to discuss product impurities, and we walk them through our lab sheets—most cases tie back to cold-chain interruptions or cross-contamination, both of which we address in our own shipping and packaging routines.

    It takes effort and know-how to keep a chemical plant running smoothly with MMS in the workflow. We employ comprehensive monitoring—not just automatic instrumentation, but also routine hands-and-eyes patrols along the process line. A trained nose and practiced eye can spot the faintest discoloration or hint of off-smell. Lab data provides reassurance but rarely serves as the first alarm. In describing MMS’ utility, our regular conversations with polymer researchers, pharmaceutical R&D staff, and materials scientists confirm its status as a go-to methylating agent due to its favorable safety and reactivity profile.

    Handling Experience and Chemical Safety Know-How

    Operators here aren’t just crunching numbers—they’re responsible for handling materials that demand precise respect. MMS is a potent alkylator and a suspected mutagen. Our plant runs regular safety briefings, and PPE selection is non-negotiable. No one steps into the MMS packout area without gloves, eye protection, and properly rated lab coats. Fresh air respirators stand ready, and spill kits lie within arm’s reach. A spilled drop receives immediate attention, scooped up and contained for hazardous disposal. We’ve learned over years of operation that fighting complacency keeps everyone safe.

    Key safety learning comes from frequent site drills. Unlike more volatile alkylating agents, MMS reacts quickly with moisture, so every drum remains double-sealed with nitrogen pads. Training includes hands-on inspections—valve integrity, color assessment, drum weight checks—alongside paperwork review. Our technical supervisors lead monthly walkthroughs, listening to operator feedback on labeling, storage, and transfer logistics. These touchpoints reveal improvement opportunities long before incident reports pile up.

    On the environmental front, we’ve engineered our wastewater treatment to handle MMS residues. Neutralization with aqueous base, followed by carbon filtration, ensures that no raw alkylating material enters municipal streams. Staffers can practically recite the waste codes, but the real lesson comes from watching our team trace a drum’s full lifecycle, from filling line to waste manifest. Every inspection uncovers small process tweaks—for instance, switching from manual to semi-automated filling lowered spillage and skin contact cases.

    Specifications Forged from Daily Production

    Marketing departments might fill up pages with numbers, but for those creating MMS at scale, only certain specs matter. We standardize on purity above 99% as measured by HPLC, no visible chromophores, water content below 0.2%, and a stable shelf profile for a minimum of six months at room temperature storage. Acidity and residue tests come straight from our own QA team’s scrapbooks. Each specification reflects a common pain point for our end users; every time a lab struggles with low-yield reactions, we double-check our own outgoing material and offer replacement if needed.

    Dimethyl sulfate and methyl iodide have been the "old standards" in methyl transfer chemistry, but MMS finds broader favor in the new generation of fine chemical research. Technicians who come to us from other companies say purity makes the difference. Impurities in MMS seed sporadic side reactions, clouding analytical results and underpinning failed batch campaigns. Our history with process upsets—like one infamous winter day when a condenser leak nearly contaminated an entire holding tank—drives home the point: nobody can afford to compromise on specification discipline.

    Addressing Common Production Challenges

    Every lot of MMS begins as a challenge and ends with collected data. Among the most common headaches: water ingress during charging, temperature drift during exothermic peaks, and valve failures during crude-phase stripping. From experience, process line staff now build redundancy—always having two operators watch charging steps, keeping spare gaskets, and monitoring jacket temperature swings minute-by-minute. Mixing rates can lead to emulsions and obscure the interface between product and wash phases, so plant staff document each phase split by hand in the batch log.

    Even downstream, the logistics staff pay close attention to temperature controls and vibration risks during transport. As the years have gone by, tracking drums by RFID and QR code gives us real-time visibility over in-transit events—catching leaks or spikes in temperature. Any signs of product instability result in a hold order until our technical team completes a full reanalysis. In over 20 years producing MMS, the most consistent lesson sounds simple: never trust a shortcut and always track the details from raw material intake to final shipment.

    Controlling Quality—Beyond the Sale

    Sending out MMS into the world involves more than filling drums and loading trucks. Every batch leaving our gates carries our reputation, and we take customer feedback seriously. Our technical support staff check with repeat buyers, reviewing reaction outcomes and even offering lab visits for troubleshooting. Many times, a simple phone conversation reveals an overlooked variable—humidity control, glassware rinse protocol, even minor temperature shifts in the reaction flask.

    We save the most meaningful written feedback in our internal logs; nothing shapes future production cycles more than learning what worked for someone else. Customers often share published research and patents citing our material in the acknowledgments. For us, that means more than any marketing slogan; it shows that quality production on the plant floor translates to real-world discovery in the lab.

    Technical support never reads from a template. Each case is different, shaped by the experience of the user and their unique requirements. Our chemists bring process insights gained from both plant runs and benchwork, giving practical advice that’s grounded in direct experience.

    Practical Comparison with Other Methylating Agents

    Plenty of alternatives exist for those trying to transfer a methyl group in a chemical synthesis. In our plant, the case for MMS comes down to two things: safety and reliability compared to older agents. Dimethyl sulfate, for example, possesses high volatility and acute toxicity. Anytime our staff handled it in earlier decades, emergency procedures ran on high alert. Methyl iodide releases toxic, corrosive vapors and leaves behind iodine byproducts, creating extra hurdles in downstream processing and waste neutralization.

    With MMS, our operators notice tangible improvements in day-to-day working conditions. The smell, while distinctive, does not linger or generate concern beyond normal ventilation requirements. In process engineering, it quickly replaces outdated methyl transfer agents due to its sharper reactivity and less-complicated handling. A colleague on our team who ran a kilo-lab processing both EMS and MMS once described the difference: “With MMS, you know the reaction will finish cleanly. With others, you’re chasing ghosts in the byproduct profile.” This sentiment matches the feedback we receive from labs worldwide.

    Comparing technical outcomes, MMS reactions run faster and generate fewer hard-to-remove residues. The simple methanesulfonic acid byproduct means purification steps require less energy and expense. Our batch documentation processes across dozens of pharma syntheses prove that fewer complaints reach our help desk when MMS batches form the alkylated product versus when customers used legacy agents.

    Continuous Improvement Driven by Daily Operations

    No chemical process remains static, least of all MMS production. Our plant invests in continuing education, sending operators and engineers for specialized upskilling and training. Improvements aren’t just about larger-scale equipment. For example, one technician suggested a minor adjustment in agitator blade height during charge-in, preventing local overheating. Staff jump on these ideas, testing small changes in pilot runs before scaling up. If an idea lowers off-spec batch rates or speeds cleanup, it becomes part of our written procedures.

    We monitor production yields and process deviations weekly, sharing the findings at shift meetings. Important points here include minimizing downtime and keeping maintenance schedules tight for vacuum lines and condensers. No batch leaves without signoff from the process supervisor, QA lead, and responsible technician. The learning goes both ways; even mid-level operators can suggest process optimizations by showing how small tweaks in flange torque or filter media impact yield. Our review meetings often feature insights picked up on the shop floor—a practice that keeps our operation grounded in practical experience.

    Environmental and Regulatory Perspective

    Regulatory oversight weighs heavily on industrial chemical production, especially for MMS, given its classification as a mutagenic substance. Our plant works hard to remain ahead of compliance requirements. Every storage drum receives clear GHS-compliant labeling. Our documentation connects each raw material shipment to a unique batch record, enabling traceability not just for audits, but also in the rare case a customer needs product recall or additional analytical support.

    Waste treatment receives as much focus as synthesis. We designed our effluent controls to capture and break down any residual MMS, using standard base quench followed by carbon beds and monitored discharge. Auditors walk our setup yearly, and we test monthly for discharge compliance. Sheltered drum storage sheds, regular emergency drill schedules, and real-time inventory checks put regulatory rules into practice every day.

    We keep abreast of best practices in chemical management. Whenever regulations change or new guidance arises, we revise internal SOPs and retrain our team. This approach ensures plant safety, product safety for our customers, and full alignment with emerging health, safety, and environmental standards worldwide.

    Supporting Research, Pharma, and Advanced Materials Development

    Many leading institutions, contract research firms, and pharmaceutical companies count on a steady, high-quality supply of MMS. We’ve watched the shift from small bench chemistry to scale-up for clinical and commercial campaigns. Regularly, research teams approach our technical staff seeking advice on maximizing methylation yield, reducing trace byproducts, or simply improving reproducibility across multiple lots.

    A large part of our recent history tracks the rise of genetic toxicology research. MMS, deployed under exacting control, induces specific mutational events that guide drug discovery and safety profiling. We supply research-grade material after extensive batch purification, each fraction checked to exceed published purity standards. Scientists point to our batch analysis data as a core part of their compound validation workflows.

    Advanced materials labs prize our MMS because of its reactivity and manageable byproduct stream. Wherever new methylated building blocks show up—in polymers, catalysts, or specialty reagents—our plant’s consistency allows for seamless cycling between kilogram and multi-tonne scale. Success in these fields ties directly to rock-solid production discipline. No amount of clever marketing can substitute for the reassurance that comes from years of reliable batch records.

    Looking Forward: Sustaining Quality and Customer Connection

    What sets us apart stems from dozens of industry cycles, countless batches, routine process optimization, and principled attention to safety and performance. We match customers not only with product, but also with the accumulated insight knotted into every shift ledger and lab notebook in our plant. The conversation doesn’t stop at shipping—real-world feedback shapes our future production and supports cleaner, safer, more innovative chemistry for everyone using methyl methanesulfonate. This experience-driven approach defines all we do, from our first shift bell to the close of each day.