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4,6-Dimethoxy-2-(Phenoxycarbonyl)Aminopyrimidine

    • Product Name 4,6-Dimethoxy-2-(Phenoxycarbonyl)Aminopyrimidine
    • Alias 4,6-Dimethoxy-2-[(phenoxycarbonyl)amino]pyrimidine
    • Einecs 623-478-3
    • 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

    630975

    Chemical Name 4,6-Dimethoxy-2-(Phenoxycarbonyl)Aminopyrimidine
    Molecular Formula C13H13N3O4
    Molecular Weight 275.26 g/mol
    Appearance White to off-white solid
    Cas Number NA
    Solubility Soluble in organic solvents such as DMSO and DMF
    Purity Typically >98%
    Storage Conditions Store at 2-8°C, protected from light and moisture
    Synonyms 2-(Phenoxycarbonyl)amino-4,6-dimethoxypyrimidine
    Structure Type Aminopyrimidine derivative

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

    Packing & Storage
    Packing 4,6-Dimethoxy-2-(Phenoxycarbonyl)Aminopyrimidine, 5g, supplied in a sealed amber glass vial with tamper-evident cap and clear labeling.
    Shipping 4,6-Dimethoxy-2-(Phenoxycarbonyl)aminopyrimidine is shipped in tightly sealed, chemical-resistant containers to prevent moisture and light exposure. It is transported in compliance with local and international chemical regulations, with clear labeling and safety documentation included. Handle with care, following standard hazardous chemical procedures. Store at room temperature, away from incompatible substances.
    Storage 4,6-Dimethoxy-2-(phenoxycarbonyl)aminopyrimidine should be stored in a tightly sealed container, away from light, moisture, and incompatible substances such as strong oxidizing agents. Store at room temperature in a cool, dry, and well-ventilated area. Appropriate chemical safety precautions should be observed, including proper labeling and use of personal protective equipment when handling the substance.
    Application of 4,6-Dimethoxy-2-(Phenoxycarbonyl)Aminopyrimidine

    Applications of 4,6-Dimethoxy-2-(Phenoxycarbonyl)Aminopyrimidine in Industrial Manufacturing

    As a specialized producer of 4,6-Dimethoxy-2-(Phenoxycarbonyl)Aminopyrimidine, we supply high-purity material directly for integration into advanced manufacturing operations. This intermediate finds critical value in the synthesis and modification steps across several regulated downstream industrial sectors.

    1. Pharmaceutical Active Ingredient Synthesis

    Major pharmaceutical manufacturers utilize our material in targeted heterocyclic core formation during pyrimidine-based API synthesis. The compound plays a specific role in amide coupling and selective methoxylation steps for small-molecule drugs, especially in oncological and antiviral research pipelines. End users require confirmed purity and consistent batch quality to meet all regulatory and validation demands.

    Industry compliance standards

    • Current Good Manufacturing Practice (cGMP, ICH Q7)
    • United States Pharmacopeia (USP, for intermediates)
    • European Pharmacopoeia (Ph. Eur.) compliance for input raw materials
    • REACH Registration for European market supply

    Typical usage ratio

    • 10–25% by molar ratio in multi-step pyrimidine scaffold assembly
    • Adjusted depending on target conversion efficiency and impurity profile
    • Stoichiometry fine-tuned for downstream coupling reactions
    • Lab-scale process validated before upscaling for GMP manufacturing

    Downstream process integration

    • Charged during N-heterocycle formation or as an aminopyrimidine precursor
    • Reacted with selective acyl chlorides or phenolic agents under inert atmosphere
    • Isolated and purified prior to further condensation or derivatization
    • Integrated into automated batch reactors with online QC for in-process control

    Final product types

    • Pyrimidine-based anticancer agents (e.g., kinase inhibitors)
    • Nucleoside analog antiviral drugs
    • Small-molecule clinical trial candidates
    • Custom reference standards for pharmaceutical research

    2. Agrochemical Research and Production

    Crop protection compound formulators use our intermediate to create novel pyrimidine-based herbicides and fungicides. The methoxy-substituted aromatic structure facilitates synthetic transformations for actives with improved selectivity and metabolic stability, helping developers meet strict residue and efficacy standards for regulated markets.

    Industry compliance standards

    • OECD Good Laboratory Practice (GLP) for premarket studies
    • EPA 40 CFR Part 174 (US pesticide approval)
    • ISO 9001:2015 for agrochemical raw material traceability
    • REACH Annex II requirements for classified substances

    Typical usage ratio

    • 5–15% w/w in key intermediate stages of active ingredient synthesis
    • Concentration adjusted for chlorination, oxidation, or ring closure efficiency
    • Ratio aligned with LC-MS impurity profile acceptance limits
    • Batch quantity determined by downstream conversion scale

    Downstream process integration

    • Added during nucleation and cyclization step for pyrimidinone herbicide preparation
    • Reacted with alkylating and acylating agents for structural modification
    • Isolated by precipitation and solvent extraction for high-purity yields
    • Transferred directly to formulation plants for final blending

    Final product types

    • Pyrimidine-derived fungicide actives (e.g., pydiflumetofen)
    • Selective herbicides for cereals and rice
    • Intermediate for seed treatment agents
    • Research compounds for agrochemical screening libraries

    3. Custom Chemical Synthesis for Fine Chemical Houses

    Custom synthesis firms incorporate this raw material into multi-step routes for diversified fine chemical manufacturing. Its unique substitution pattern enables access to specialized building blocks required for pigments, dyes, and advanced electronic chemical intermediates. Chain of custody throughout supply ensures strict batch traceability.

    Industry compliance standards

    • ISO 9001:2015 (Quality Management System)
    • GMP for fine chemicals (where customer-spec required)
    • SOCMA ChemStewards® for environmental, health, and safety (EHS)
    • Material regulatory screening via ECHA database

    Typical usage ratio

    • 5–30% as a key intermediate, dependent on downstream molecule complexity
    • Ratio calculated by final theoretical yield from process flow simulation
    • Adjusted for side-product minimization in high-purity applications
    • Optimized by customer-driven route development

    Downstream process integration

    • Loaded in high-shear glass reactors for heterocycle fusion reactions
    • Undergoes acylation or coupling for pigment or dye precursor production
    • Stage-gated with intermediate QC and impurity tracking
    • Supplied as in-situ solution or isolated solid as project-specific needs

    Final product types

    • Specialty colorants for plastics and printing inks
    • OLED and liquid crystal display intermediates
    • Photostable dyes for electronics
    • Custom heterocyclic building blocks for further synthesis

    4. Reference Standard and Analytical Reagent Supply

    Analytical service providers and research institutions purchase our material as a core reference standard for chromatographic and spectrometric method calibration. Its defined chemical structure supports validation of compound libraries and impurity profiling in regulated laboratory environments.

    Industry compliance standards

    • ISO/IEC 17025 accreditation for analytical laboratories
    • USP Reference Standards protocols
    • GLP for laboratory reagents
    • Traceable purity certificates with COA and MSDS accompanying each shipment

    Typical usage ratio

    • 1–5 mg per calibration run for instrument validation
    • Aliquoted based on required sensitivity and detection limits
    • Supplied in multi-gram lots for method development batches
    • Stock solution prepared in accredited laboratory conditions

    Downstream process integration

    • Weigh-in for HPLC, GC-MS, or NMR calibration testing
    • Dissolution into certified solvents for standard solution preparation
    • Stored under nitrogen or argon to maintain stability
    • Used as process control for impurity profiling

    Final product types

    • Certified reference standards for pharmaceutical QC labs
    • Calibration solutions for instrument manufacturers
    • Analytical reagents for academia and CROs
    • Internal standards for toxicological research
    Free Quote

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    Certification & Compliance
    More Introduction

    Introducing 4,6-Dimethoxy-2-(Phenoxycarbonyl)Aminopyrimidine: Developing Solutions Through Experience

    Over the past decade, our teams have spent long hours in labs and pilot plants, tuning the synthesis route for 4,6-Dimethoxy-2-(Phenoxycarbonyl)Aminopyrimidine. Those who work with advanced pyrimidine-based intermediates will understand why a compound like this finds its place not just on a product list but often in the heart of real-world research and manufacturing.

    What Defines Our 4,6-Dimethoxy-2-(Phenoxycarbonyl)Aminopyrimidine

    The model our chemists deliver begins with a distinct purity profile. We focus on crystalline forms with low-residual solvent measured batch by batch on high-performance liquid chromatography. Loss on drying, trace metals, and assay results all stay within strict parameters, because experienced processors recognize that these differences reveal themselves in downstream reactions. Such control doesn’t come from automated scripts but from focused plant engineering, regular calibration, and teams who notice when something feels slightly off in a batch, often before machines do.

    Specifications Shaped by Years

    Raw data matters—assay values often fall at 99% or higher thanks to custom filtration and multiple recrystallizations during isolation. We keep chloride, sulfate, and heavy-metal contaminants well below typical compendial limits. Moisture content stays low—the kind troubleshooting chemists want, since water can twist pyrimidine reactivity in unwanted ways. What gets lost in most product sheets—grain size, bulk density, flow behavior—has a practical effect in plant settings. End users report far lower clogging and dust formation compared to generic competitors. We attribute that to the narrower particle-size distribution our line delivers, coupled to a time-tested process flow that resists introducing fines or sticky agglomerates.

    Why Real-World Synthesis Relies on Consistency

    One recurring question in this industry circles back to batch repeatability. Many have ordered advanced intermediates only to discover, on arrival, shifting color, unexpected melting-point ranges, or persistent off-odors. With 4,6-Dimethoxy-2-(Phenoxycarbonyl)Aminopyrimidine, we keep active logs of every shift in crystallization conditions. Plant operators and analysts review trendlines of previous yields and impurity spikes, offering an extra layer of hands-on judgment. For us, this is more than regulatory compliance; sudden shifts in material performance lead to costly troubleshooting downstream.

    Practical Applications in Research and Industry

    This compound’s value emerges wherever modified pyrimidines are central. Our farm partners investigating novel agrochemicals often select this core as a foundation for targeted synthesis. It carries two methoxy groups at the 4- and 6-positions, creating characteristic reactivity that facilitates coupling reactions and etherifications. Its phenoxycarbonyl-amino substituent invites derivatization—there’s ample room to plug in optimizing functional groups, or, for medicinal teams, to modulate biological activity. Those crafting kinase inhibitors or enzyme modulators mention our batches specifically support clean downstream transformations without high levels of residual byproducts.

    Some smaller-scale labs in peptide and oligonucleotide synthesis use our intermediate for selective coupling steps, noting stronger control over side reactions and unwanted hydrolysis. As more pharmaceutical projects move toward complex scaffolds, we see a steady growth in demand for such finely calibrated intermediates. Rather than simply delivering a chemical, we often consult on solvent compatibility and decomposition risks in real-life operations—fewer surprises, better yield, and easier regulatory documentation.

    A Perspective From Inside the Plant: How This Compound Sets Itself Apart

    Early on, many customers drew comparisons to products sourced from quick-turnaround synthesizers or multi-product batch facilities. Differences appear in actual use. For 4,6-Dimethoxy-2-(Phenoxycarbonyl)Aminopyrimidine, we manufacture in dedicated vessels, using materials of construction and cleaning regimes that eliminate cross-contamination from closely related pyrimidines or amide derivatives. Process validation, carried out with transparency and traceability, reassures buyers and auditors that no unapproved species sneak into their regulatory filings. Anyone familiar with the tension that comes from re-testing lots will understand the peace of mind this discipline brings.

    The choice to focus on consistency over margin was deliberate. Market pressure often leads others to reduce monitoring or cut corners on raw material quality. We source high-purity dimethoxy precursors and monitor phenoxycarbonyl reagents for common aromatic impurities that would otherwise become costly headaches at later stages in synthesis. Lab teams keep method records open for review; we’ve seen how small impurities blossom into significant failures in pilot-scale production, prompting us to invest upstream and document every adjustment to temperature profiles, agitator speed, and seeding times. The product our clients receive reflects that obsession with detail.

    Lessons Learned From Customer Feedback

    Several years ago, a research group attempting to crystallize challenging analogs sent a detailed report on solubility changes tied to trace solvent inclusion in the intermediate. Inspired by their observation, we improved the vacuum-drying step and installed on-line monitoring for solvent evolution, preventing repeated moistening of the lot. Not only did customer complaints vanish, but subsequent analytical work showed a marked drop in byproduct formation. Trust grows as these experiences build up year by year.

    Another manufacturer in the specialty enzymes field highlighted instability they’d spotted in certain competitor samples—the color drifted after exposure to light. We traced this to a photolabile contaminant from a shortcut in a competing supplier’s process. Since then, we’ve automated purity profiling for photoreactive trace byproducts as part of our standard batch release, giving our end users extra insurance during long-term storage and transport.

    Understanding the Stakeholders: From Lab Bench to Shipping Dock

    Our workforce—analysts, engineers, packagers—finds themselves pulled into discussions with everyone from plant procurement officers to regulatory affairs experts and formulation chemists. We approach requests about 4,6-Dimethoxy-2-(Phenoxycarbonyl)Aminopyrimidine from all angles, whether the end-use sits in crop protection, animal health, or emerging drug platforms. The recurring pain point for many customers has been uneven documentation from the broader market. Instead of sending generic certificates, we load each shipment dossier with batch-level HPLC runs, NMR confirmation, and, when prompted, IR and elemental analysis. Anyone evaluating a critical synthetic intermediate for GMP synthesis knows that extra level of transparency can remove months of downstream paperwork. We view it as insurance—a safeguard for our partners, protecting their timelines and investments.

    What Sets Our Approach Apart: Workflow Adjustments and Technical Support

    Countless times, buyers place orders not just for finished product but for extended support—how will this intermediate behave under specific pH cycling or after prolonged exposure to high-shear mixing? Our technical specialists often head back to old batch notes, pulling up past cases to offer real-world advice. For example, clients shifting from bench-scale to multi-ton runs need assurance the same material attributes persist over time. As we’ve ramped up output, tight controls at each step—from reaction quench to filtration—ensure uniformity batch to batch. Sometimes, engineering tweaks emerge from customer-led troubleshooting. After one customer found filtration rates slowed markedly at colder seasonal temps, plant operators adopted a modified filter aid and adjusted cycle timing, restoring throughput and lowering operating costs. In these interactions, the distinction between manufacturer and partner quietly fades away.

    Not every producer can or chooses to invest in lot-by-lot discussion or documentation. From our vantage, this effort pays unexpected dividends. Continued dialogue with academic groups, Fortune 500 firms, and niche biotech startups keeps us ahead of regulatory shifts, supply chain concerns, and technical bottlenecks. We update our plant protocols regularly—sometimes only after a partner points out an emerging analytical issue. This responsive feedback loop creates a more robust supply solution, rather than a static product that risks obsolescence.

    Differences From Other Products: More Than Just a Molecule

    An easy mistake lies in comparing intermediates solely by chemical structure or price-per-kilo. Some market alternatives come from multi-use plants where cleanout protocols lag, or where analytical verification does not reach the same depth. Ask anyone who has had a project derailed by odd spectral interferences how important uncompromising plant discipline proves in high-consequence supply chains. For us, purity means not just surpassing standard specifications but eliminating trace liabilities—from related compounds, heavy metals, or manufacturing additives that resist detection in coarse-grained QC testing.

    Compared to more generic pyrimidine intermediates, ours occupies a more specialized space—designed from inception for advanced derivatization and reliable scale-up. Academic synthesis routines often use off-the-shelf, minimally processed versions to save budget. These compounds work for early-stage proof-of-concept, but as projects mature, so must the material. Our manufacturing-built version offers repeatable reactivity and supply predictability, which keeps larger projects from stalling during tech transfer or regulatory review.

    Other intermediates, even close cousins in the pyrimidine family, show different risk profiles when scaled. Differences in substitution patterns or physical properties tilt the odds toward unwanted side reactions, instability during storage, or inconsistent performance when used under stress (routes involving strong acid or base, elevated temperature, or protracted isolation steps). Our long-running investment in downstream performance monitoring—tracking color, melt point, and impurity drift through long-haul storage—demonstrates that subtle choices made during synthesis and isolation make all the difference between success and costly rework.

    Collaborative Growth: Sharing Experience With the Field

    Manufacturing 4,6-Dimethoxy-2-(Phenoxycarbonyl)Aminopyrimidine at scale built muscles in process design, analytical control, and customer engagement. Each year brings new questions from working scientists—how might it behave in a new heterocycle synthesis, or what happens under new catalytic conditions? Often, we learn alongside our customers, adapting protocol not just to our own workflow, but to the evolving landscape of chemical research and industrial practice. We share data, explore new analytical methods, and fine-tune our own batch records when confronted by new applications or challenges. This transparency and ongoing investment in improvement anchors us and builds trust in both directions.

    Supporting Safe, Sustainable, and Transparent Chemistry

    Choices at the manufacturing level impact more than just cost or yield. By minimizing solvent waste, controlling energy use in drying and isolation, and constantly evaluating safe handling protocols for 4,6-Dimethoxy-2-(Phenoxycarbonyl)Aminopyrimidine, we contribute to a safer workplace, a cleaner environment, and a more responsible chemical supply. End users, from chemists in pharma research to engineers in large-scale synthesis, benefit from confidence that their intermediate arrives every time to a reproducible quality standard—backed by real data and accessible expertise.

    Through steady investment, experienced teams, and a willingness to adjust workflows based on hands-on experience, we continue to shape how advanced pyrimidine intermediates contribute to breakthroughs in science and industry. This commitment, grounded in hundreds of batches and ongoing feedback, defines what customers can expect from our 4,6-Dimethoxy-2-(Phenoxycarbonyl)Aminopyrimidine: more than a chemical, a proven solution for building the molecules of tomorrow.