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4,6-Dimethoxypyrimidine

    • Product Name 4,6-Dimethoxypyrimidine
    • Alias 4,6-Dimethoxy-1,3-pyrimidine
    • Einecs 226-744-7
    • 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

    800323

    Chemical Name 4,6-Dimethoxypyrimidine
    Molecular Formula C6H8N2O2
    Molecular Weight 140.14 g/mol
    Cas Number 3008-73-5
    Appearance White to off-white solid
    Melting Point 102-104°C
    Boiling Point 284-286°C
    Density 1.20 g/cm³
    Solubility Soluble in organic solvents like DMSO, methanol
    Smiles COc1cc(OC)nc(n1)
    Synonyms 4,6-bis(Methoxy)pyrimidine
    Refractive Index 1.517 (predicted)
    Purity Typically ≥98%
    Storage Store at room temperature, away from moisture and light
    Pubchem Cid 12028

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

    Packing & Storage
    Packing 100-gram 4,6-Dimethoxypyrimidine is packaged in a sealed amber glass bottle with a chemical-resistant label detailing product and hazard information.
    Shipping 4,6-Dimethoxypyrimidine is typically shipped in tightly sealed containers to prevent moisture or contamination. It should be transported under ambient conditions, away from sources of heat, ignition, and incompatible substances. Proper labeling and documentation in accordance with local regulations are required to ensure safe and compliant delivery.
    Storage 4,6-Dimethoxypyrimidine should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from incompatible substances such as strong oxidizing agents. Protect it from moisture and direct sunlight. Store at room temperature and ensure the storage area is clearly labeled and suitable for chemicals to prevent accidental exposure or contamination.
    Application of 4,6-Dimethoxypyrimidine

    Applications of 4,6-Dimethoxypyrimidine in Industrial Manufacturing

    As a core manufacturer of 4,6-Dimethoxypyrimidine, we serve specialized industrial segments where this heterocyclic compound delivers critical functionality in chemical synthesis. Below, we detail the primary application scenarios based on established global market uses, with an emphasis on real-world formulation practices, compliance requirements, downstream integration, and final product types.

    1. Agrochemical Intermediate in Selective Herbicide Synthesis

    Our bulk material supports global crop protection manufacturers as an essential building block for several sulfonylurea and triazolopyrimidine herbicides. Formulators integrate it at the early condensation and ring-closure stages to introduce specific pyrimidine substituents, underpinning selective weed control profiles for major field and specialty crops. Regulatory bodies closely monitor input materials across synthesis, especially for active ingredient traceability and residual management in food systems. End-users require consistent quality and trace elemental control to meet multi-region market entry certifications.

    Industry compliance standards

    • Food and Agriculture Organization (FAO) specification for Active Ingredients
    • EPA FIFRA regulations for agrochemical inputs (United States)
    • European Regulation (EC) No 1107/2009 for plant protection products
    • China GB 2763 MRLs for pesticide residues

    Typical usage ratio

    • 3–8% of total input mass for key pyrimidine ring synthesis, adjusted based on crop species, desired selectivity, and target molecule load

    Downstream process integration

    • Enters condensation reaction stage with aromatic amines or sulfonyl precursors; critical in forming the herbicide’s core scaffold prior to further functionalization and formulation

    Final product types

    • Sulfonylurea herbicide active ingredients (e.g., nicosulfuron, rimsulfuron, chlorimuron)
    • Triazolopyrimidine-class selective herbicides
    • Suspension concentrates and wettable granules for field application

    2. Pharmaceutical Intermediate for Antiviral and Anticancer APIs

    Pharmaceutical sectors use our material as a pyrimidine source in several small-molecule drug API synthesis routes, particularly nucleoside analogues and kinase inhibitors. Synthesis teams introduce it into stepwise alkylation or cross-coupling chains to achieve precise 4,6-substitution patterns, crucial for biological activity. Input control ensures API producers meet international GMP, impurity profiles, and pharmacopoeial monographs, especially for regulated global markets and high-value oncologic, virology, and immunology drug pipelines.

    Industry compliance standards

    • International Conference on Harmonisation (ICH Q7) GMP guidelines
    • United States Pharmacopeia (USP), European Pharmacopoeia (EP) for active substances
    • China NMPA Drug Master File protocols
    • FDA Drug Substance Impurity Limits (ICH Q3A)

    Typical usage ratio

    • 1.5–6% relative to primary nucleoside or kinase scaffold, optimized per API target and process route; refined based on isomer selectivity and minimum impurities

    Downstream process integration

    • Introduced in early-stage pyrimidine alkylation or halogenation steps; enables controlled ring modification prior to downstream API finishing reactions and purification

    Final product types

    • Nucleoside anti-viral drugs (e.g., lamivudine intermediates)
    • Pyrimidine-based anticancer kinase inhibitors
    • Finished API powder for formulation into tablets, capsules, injections

    3. Intermediate in Veterinary Pharmaceutical Synthesis

    Animal health manufacturers depend on this compound during the multi-step synthesis of antiparasitic and anti-infective actives, especially those exploiting pyrimidine ring structures for efficacy against protozoal and helminth targets. Compliance with veterinary pharmacopeias and residue limits in edible animal products strongly influence raw material traceability and input validation along the supply chain for both domestic and export veterinary formulations.

    Industry compliance standards

    • Veterinary International Cooperation on Harmonization (VICH) GLs for APIs
    • European Pharmacopoeia Monographs for veterinary actives
    • Codex Alimentarius for veterinary drug residues in food animals
    • Japan Pharmacopoeia, Veterinary Section

    Typical usage ratio

    • 2–7% by mass in precursor stage synthesis, varying by active ingredient and analytical yield requirements

    Downstream process integration

    • Feeds into cyclization or methylation steps of veterinary active synthesis, often preceding side-chain extension and salt formation for improved bioavailability

    Final product types

    • Antiparasitic bulk actives, such as pyrimidine-based coccidiostats
    • Veterinary anti-infective intermediates
    • Premix and injectable finished dosage forms for livestock

    4. Intermediate for Specialty Dyestuff Synthesis

    Dye and pigment producers select this pyrimidine derivative to construct advanced chromophore scaffolds used in printing inks and polyester fiber coloration. R&D and production specialists rely on its high purity to achieve clear, bright color yield and stability, using it at the nucleophilic substitution or condensation stages. Commercial viability requires raw material controls aligned with global textile and ink chemical safety frameworks, especially with rising end-market demand for traceable substances and limited aromatic amine impurities.

    Industry compliance standards

    • OEKO-TEX Standard 100 – Restricted Substances List for dye formulations
    • REACH Annex XVII limitations on aromatic amines
    • ZDHC Manufacturing Restricted Substances List (MRSL)
    • ISO 105 textile colorfastness testing

    Typical usage ratio

    • 4–10% by weight in key condensation or azo coupling reactions, modulated by desired dye intensity and substrate compatibility

    Downstream process integration

    • Inserted into nucleophilic aromatic substitution or ring-fusion steps to build chromophore backbone prior to azo or anthraquinone derivative finalization

    Final product types

    • Pyrimidine-based disperse and reactive dyestuffs
    • High-yield textile colorants for polyester and acetate fibers
    • Specialty inks for packaging and digital printing
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