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2-Methylsulfonyl-4,6-Dimethoxypyrimidine

    • Product Name 2-Methylsulfonyl-4,6-Dimethoxypyrimidine
    • Alias MSMP
    • Einecs 809-923-6
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
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    Specifications

    HS Code

    212550

    Chemical Name 2-Methylsulfonyl-4,6-Dimethoxypyrimidine
    Molecular Formula C7H10N2O4S
    Molecular Weight 218.23 g/mol
    Cas Number 65200-80-8
    Appearance White to off-white solid
    Melting Point 99-102 °C
    Solubility In Water Slightly soluble
    Smiles COC1=NC(=NC(=C1)OC)S(=O)(=O)C
    Inchi InChI=1S/C7H10N2O4S/c1-14(11,12)7-8-5(9-6(7)13-2)10-3/h1-3H3
    Storage Conditions Store in a cool, dry place

    As an accredited 2-Methylsulfonyl-4,6-Dimethoxypyrimidine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Sealed 250g amber glass bottle with tamper-evident cap. White printed label displaying chemical name, quantity, safety icons, and storage instructions.
    Shipping 2-Methylsulfonyl-4,6-Dimethoxypyrimidine is shipped in tightly sealed containers to prevent moisture or air exposure. It is packaged according to chemical safety regulations, labeled with appropriate hazard information, and typically transported by certified carriers. Temperature and handling instructions are provided to ensure product integrity and safe delivery to the destination.
    Storage 2-Methylsulfonyl-4,6-dimethoxypyrimidine should be stored in a cool, dry, and well-ventilated area, away from direct sunlight and sources of heat or ignition. Keep the container tightly closed and clearly labeled. Avoid exposure to moisture and incompatible materials such as strong oxidizing agents. Store at room temperature, and follow all relevant safety and environmental regulations for chemical storage.
    Application of 2-Methylsulfonyl-4,6-Dimethoxypyrimidine

    Applications of 2-Methylsulfonyl-4,6-Dimethoxypyrimidine in Industrial Manufacturing

    As a committed manufacturer, we supply 2-Methylsulfonyl-4,6-Dimethoxypyrimidine to specialized sectors that require precise chemical intermediates for active ingredient synthesis and complex transformation steps. This material supports downstream producers in regulated environments, delivering targeted value for advanced synthesis demands.

    1. Synthesis of Sulfonylurea Herbicide Intermediates

    Our material is a designated core building block in the multi-step synthesis of sulfonylurea herbicides, serving as a critical pyrimidine intermediate in agrochemical manufacturing plants. Research-based customers rely on its purity for efficient ring-functionalization, specifically in the preparation of key intermediates such as 4,6-dimethoxypyrimidine derivatives required for high selectivity herbicide actives. Production chemists introduce it during the condensation phase, driving targeted substitution and achieving consistent batch-to-batch yields demanded by large-scale crop protection producers.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • ISO 9001:2015 Certified Quality Management Systems
    • REACH (EU Regulation No 1907/2006) Registration Requirements for Pesticide Precursors
    • GB 2763 National Food Safety Standard for Maximum Residue Limits in China

    Typical usage ratio

    • Formulation ranges from 5% to 18% by mass in the condensation feedstock, depending on desired throughput and reaction scale; optimized for stoichiometric efficiency with alkylating agents or sulfonation steps.

    Downstream process integration

    • Introduced during pyrimidine ring construction and methylsulfonyl functionalization; used before final formation of the urea linkage in closed-system reactors.

    Final product types

    • Technical grade sulfonylurea herbicide actives (e.g., metsulfuron-methyl, rimsulfuron)
    • Granular and wettable powder crop protection formulations
    • Water-dispersible tablets for cereal and corn crops

    2. Pharmaceutical Intermediate for Antiviral Drug Synthesis

    This compound is a specialized intermediate in the manufacture of certain pyrimidine-based antiviral pharmaceuticals, required by API producers for heterocyclic coupling reactions. It is directly involved in the construction of pharmacophores found in experimental nucleoside analogues and small-molecule candidates. Operations teams in GMP-certified plants use this material during the early-to-mid stages of molecule assembly, where strict trace control and low impurity specifications are essential for further downstream transformations leading to clinical-grade APIs.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • EU GMP Vol IV for Intermediates and Starting Materials
    • USP <1043> Ancillary Materials for Cell, Gene, and Tissue-Engineered Products
    • Chinese Pharmacopoeia (ChP) Intermediate Raw Material Quality Requirements

    Typical usage ratio

    • Usage concentration generally lies within 3% to 12% of total input in stepwise heterocycle synthesis; determined by target nucleoside scaffold and specific coupling yields validated during process validation runs.

    Downstream process integration

    • Fed into batch reactors at the pyrimidine scaffold assembly stage, followed by methoxyl functionalization and subsequent condensation with sugar moieties or alternative heterocycles under controlled-temperature protocols.

    Final product types

    • Registered API intermediates for antiviral drugs
    • Nucleoside analogue small-molecule drug substances
    • Specialty pharmaceutical intermediates for contract development and manufacturing organizations (CDMOs)

    3. Fine Chemical Intermediate for Agrochemical Research and Development

    Global agrochemical companies require this pyrimidine derivative for the rational design and screening of active ingredients within new mode-of-action projects. Chemists in advanced R&D facilities introduce it in combinatorial libraries for SAR (structure-activity relationship) studies, integrating the compound in custom synthesis workflows. Its precise reactivity and stable sulfone group allow for routine analogue expansion, informing field test evaluations and pilot batch upscaling. Research managers rely on granular analytical control, enabling reproducibility and compliance with innovation gate requirements.

    Industry compliance standards

    • OECD Good Laboratory Practice (GLP) Guidelines
    • ISO/IEC 17025 Accredited Laboratory Standards
    • US EPA TSCA Chemical Substance Inventory
    • Japan CSCL (Chemical Substances Control Law) Screening Protocols

    Typical usage ratio

    • Library synthesis inputs range from 2% to 9% by mass; adjusted according to the screening platform and target array size for robust high-throughput experimentation.

    Downstream process integration

    • Incorporated into research-scale library generation, often as the principal nucleophile or electrophile to provide structurally distinct variants for testing; purified by flash chromatography or crystallization prior to bioassay submission.

    Final product types

    • Agrochemical lead compound libraries
    • Analytical reference standards
    • Seed compounds for greenhouse and preliminary field evaluation

    4. Heterocyclic Intermediate for Custom Synthesis Houses

    Contract manufacturers and custom synthesis providers specify this material as a key functionalized heterocycle for advanced pyrimidine derivatives. Their client projects often require it during scaffold modification, especially to generate methoxylated sulfonyl frameworks for non-exclusive life science and materials targets. Laboratory teams apply it in targeted transformation steps, maximizing coverage of possible derivatives for licensing or proprietary development, adhering strictly to project-specific documentation rules and quality assurance systems.

    Industry compliance standards

    • ISO 13485 Quality Management for Medical Device Intermediates (when destined for medtech use)
    • SHEQ (Safety, Health, Environment, Quality) Auditing Protocols
    • Client-specific NDA-driven QC and documentation trails
    • RoHS (Restriction of Hazardous Substances) Compliance when requested

    Typical usage ratio

    • Typically dosed from 4% to 16% in multi-stage synthesis sequences; adjusted to match the target output or the nature of downstream functional group modifications.

    Downstream process integration

    • Charged at the scaffold diversification stage, sometimes after initial methylation or sulfonylation steps; compatible with microwave-assisted syntheses and parallel reaction modules to speed up development cycles.

    Final product types

    • Patent-protected chemical intermediates
    • Pyrimidine-based specialty monomers
    • Non-agrochemical heterocyclic intermediates for advanced R&D
    Free Quote

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    Certification & Compliance
    More Introduction

    2-Methylsulfonyl-4,6-Dimethoxypyrimidine: Expert Insight from the Manufacturer’s Floor

    Modern Chemistry’s Role in Crop Protection

    Walk through the production floor in a chemical manufacturing plant and the world looks different from a distributor’s warehouse or a trader’s desk. We touch the raw materials, watch reactions bubble, test purity, and see how small choices in batch conditions lead to real-world differences for people using our products. 2-Methylsulfonyl-4,6-Dimethoxypyrimidine—often abbreviated as MSDMP—offers a look into how production realities shape outcomes for customers working in agriculture, fine chemistry, and process research.

    Behind the Scenes: Manufacturing Quality in Every Batch

    Take a dive into how MSDMP goes from theory to high-quality substance. Producing this compound demands tight control at every point—starting with raw materials free of trace impurities, adding each reactant under carefully managed temperatures, and keeping moisture at bay to avoid unwanted byproducts. Every lot passes strict analytical checks: we run HPLC, GC-MS, and NMR tests on-site, not to meet red tape, but to ensure what leaves our doors meets the bar we set for purity and yield. Small deviations can mean trouble for herbicide makers down the line, so diligence up front saves headaches later.

    MSDMP’s Place in Synthesis Chemistry

    Many customers approach us with a specific project in mind—usually as an intermediate in herbicide synthesis, especially for sulfonylurea classes. This pyrimidine derivative provides stability and compatibility with downstream nucleophilic substitutions. In process terms, its clean reactivity profile stands out. Where some analogues throw off hard-to-remove byproducts or require tricky purification, our process refinements give a product that helps downstream synthesis run smoother. For anyone formulating agrochemicals at scale, those efficiencies translate to fewer plant stoppages and less material lost per batch run.

    Technical Specifications: What Matters in Practice

    Talk with end-users and patterns emerge around what info they really care about. Rather than running off a list of technical specs, we zero in on batch-to-batch consistency, solubility in target solvents, color and odor (because even off-white powders raise questions), and performance under different reaction conditions. We find that most of our partners care more about how our product holds up under scale-up and pilot-plant conditions than about niche properties. Some of our competitors don’t share this focus, and their customers run into surprises if quality shifts from order to order. That underlines why process discipline on the shop floor matters so much.

    Purity Concerns and the Ripple Effect Downstream

    Impurities in a synthesis intermediate like MSDMP ripple through every step downstream. In early years, we used off-the-shelf solvents and weathered a few headaches over byproduct contamination. Field complaints (gelling in reactors, unexpected color formation, or extra step in purifying active ingredient) pushed us to source more carefully. Now, we custom-distill our major solvents and test minor ones ourselves. Most of our direct customers—industrial chemists and formulation teams—notice these efforts. The results show up as higher conversion rates and cleaner isolation in their own syntheses.

    Stability and Storage: Lessons from the Floor

    Warehousing teams know that too much humidity or swung temperatures can cost more than a failed audit. MSDMP tends to show robust storage stability when packaged right, using multilayer barrier drums and desiccant inlets. Where earlier packages let in small amounts of moisture, we saw caking and discoloration months down the line; with our newer protocols these defects have nearly vanished. Nothing substitutes for direct manufacturer efforts here—third-party storage just doesn’t offer the feedback loops we rely on to fine-tune packaging and logistics.

    Why MSDMP Differs from Lookalike Pyrimidines

    Plenty of products have structural similarity to MSDMP, but not all perform the same way in a process environment. Other methylsulfonyl pyrimidines sometimes show higher reactivity in side reactions, particularly at elevated pH. Users trying to substitute another pyrimidine often return with anecdotes about stubborn byproducts or fouling in flow reactors. Structure-activity relationships matter, yet so does the “invisible” pedigree of process design. Years of practice have shown us that small changes in synthesis or purification lead to big changes in how an intermediate like MSDMP handles during scale-up. This difference rarely shows up in a data sheet or catalog summary.

    Applications: Not Just an Intermediate

    Many customers recognize MSDMP’s leading role as a building block for high-value agrochemicals—especially sulfonylurea herbicides. Some formulators use it in research on new actives, leveraging its electron profile to create structures with better selectivity and crop safety. In a few cases, we’ve seen demand in sectors like pharmaceutical intermediates and speciality fine chemicals, where its dimethoxy functionality opens doors for further elaboration. We rarely see it used as an end product, but the diversity of demand keeps us tuned in to both quality and process adaptability.

    Batch Feedback: Closing the Loop Between Manufacturer and User

    Direct communication with customers plays a huge role in refining our production. Over the years, we’ve learned that the best insights don’t come from spec sheets but from troubleshooting real-world plant runs—be it solubility in off-spec solvents, issues with dust handling during transfer, or stability across temperature swings. We keep an open line with several long-term partners who run pilot-plant tests and feed their data back to us, shaping improvements in drying protocols and packing systems.

    Environmental and Safety Considerations in Modern Production

    Current regulatory demands push all manufacturers to minimize waste, energy use, and exposure risks. Our switch to closed systems for major steps nearly eliminated fugitive emissions, reducing worker exposure and cutting raw material waste. On the environmental front, solvent recycling and minimization practices led to measurable drops in our ecological footprint. Years ago, disposal costs drove these changes, but now it’s about doing the right thing for our crew and the communities next door. Every process tweak we implement aims to balance efficiency, safety, and responsibility.

    Comparing Real-World Performance to Competitor Products

    All MSDMP is not born equal. Some processes (especially those chasing lowest cost) yield powders with residual solvent, fluctuating purity, or microcontaminant traces that only show up at the large scale. We’ve tested competitor samples in our own labs, running them through typical herbicide synthesis and purification. Our experience shows their batches don’t always dissolve cleanly or maintain color stability over time, and a handful produce higher waste levels downstream. With direct control over both process and QA testing, we keep these issues in check before the product leaves our plant. It’s a level of scrutiny that distributors or relabelers rarely sustain, and the result is greater consistency for industrial chemists working under real deadlines.

    Responding to Evolving Customer Needs

    As regulatory pressures and environmental standards shift, so do customer priorities. In recent years, we’ve seen more requests for documentation on trace impurities, toxicology reviews, and even customized packing solutions to support unique logistics footprints. Rather than react as a distant supplier, we work closely with clients, debugging process issues or adapting batch size to sync with their campaign schedules. One small run for a field trial here, a hundred kilos for a scale-up there—this flexibility only works because we own the manufacturing, control the process, and welcome real technical dialogue. When customers face changing formulation rules or new analytical demands, we’re already prepping solutions instead of waiting for trouble.

    MSDMP for R&D and Process Innovation

    R&D labs love a reliable intermediate—one they can introduce with confidence into new synthetic designs. MSDMP, with consistent performance, gives researchers room to innovate. In our experience, R&D teams are less interested in the generic “white to off-white powder” description and more in the way our product handles: consistent melting points batch to batch, clean solubility profiles in both polar aprotic solvents and alcohols, and absence of those “unknown peaks” that slow down analytical work. Smoother workups and reproducible downstream yields let their best people spend less time troubleshooting and more time inventing.

    Seeing Value Beyond Price per Kilo

    On paper, many procurement teams could chase the lowest headline price hoping for budget wins. Walk the shop floor or chemist’s bench, and the far costlier danger is shoddy input material—one off batch can cost more in lost time, material scrapping, and overtime than the entire raw material bill. Most long-term partners see past pennywise approaches, recognizing that a few savings up front pale next to the cost of a production miss. Consistent, verified supply lets them de-risk projects and focus on hitting tight field trial deadlines.

    Adapting Logistics and Distribution

    MSDMP’s sensitivity to moisture means careful thought goes into packing and shipping. We worked through some growing pains—swapping out steel drums that picked up condensation for composite drums with custom liners. The transition cut down on returns and field complaints. Our logistics team coordinates directly with transport partners, making contingency plans for any hold-ups or environmental extremes along the way. Instead of viewing logistics as an afterthought, we treat every shipment as the start of the customer’s production run, not the end of ours.

    Supporting Analytical Demands: Beyond the COA

    Analytical chemists push us for more than generic certificates of analysis. They want granularity—details on minor impurities, full NMR runouts, proof that the process locks out critical contaminants, and stability data across variable storage conditions. We built our QA team’s expertise around delivering such data quickly and transparently. In a world where regulatory scrutiny increases, those habits pay off: customers can clear their own audits and regulatory filings with confidence in the data we provide. That closes the loop between manufacturing reality and the regulatory landscape shaping product lifecycles.

    Lessons Learned on the Manufacturing Floor

    Direct experience on the plant floor changes how we view MSDMP’s lifecycle. Little problems—solvent lot variability, a drop in nitrogen purge flow, or a dusty transfer—add up to big problems at the user end. Years of hands-on troubleshooting shaped our checklists and batch signoffs. Working through a succession of improvement cycles, we cut out most “mystery variability” upstream, saving time and trouble for our users. What we put into a kilo of MSDMP leaves its mark on the hundreds of tons of herbicide or fine chemical that follow. For us, product quality is never an abstraction—it’s the sum of every hour spent testing and refining.

    Final Thoughts: MSDMP as a Reflection of Manufacturing Values

    2-Methylsulfonyl-4,6-Dimethoxypyrimidine isn’t just a chemical we make and sell. It’s a test of our discipline, our commitment to partners, and a marker for the culture we nurture on the floor. Process innovation, quality assurance, safety, and environmental stewardship all come together in every lot we release. Our story with this compound has been one of continuous learning—responding to customer needs, tackling new technical demands, and staying ahead in a shifting regulatory picture. We see every ton shipped not as a finished commodity but as a living link to all the growers, scientists, and manufacturers who rely on us getting it right.