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Pyrimidine

    • Product Name Pyrimidine
    • Alias PYR
    • Einecs 206-992-3
    • 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
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    Specifications

    HS Code

    565530

    Chemical Name Pyrimidine
    Molecular Formula C4H4N2
    Molar Mass 80.09 g/mol
    Appearance Colorless liquid
    Density 1.016 g/cm3
    Melting Point -22 °C
    Boiling Point 123-124 °C
    Solubility In Water Miscible
    Cas Number 289-95-2
    Chemical Structure Six-membered aromatic ring with two nitrogen atoms at positions 1 and 3

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

    Packing & Storage
    Packing Pyrimidine is packaged in a 500 mL amber glass bottle with a secure screw cap, safety labeling, and hazard symbols displayed.
    Shipping Pyrimidine is shipped as a hazardous chemical, typically in tightly sealed containers to prevent leaks and evaporation. It should be stored and transported in cool, well-ventilated conditions, away from sources of ignition. Proper labeling and documentation are required according to international regulations for handling flammable, toxic substances during transit.
    Storage Pyrimidine should be stored in a cool, dry, well-ventilated area away from sources of ignition and incompatible substances such as strong oxidizers and acids. Keep the container tightly closed and properly labeled. Store in a chemical-resistant container, protected from light and moisture. Follow all relevant safety guidelines and local regulations for hazardous chemicals during storage.
    Application of Pyrimidine

    Applications of Pyrimidine in Industrial Manufacturing

    Pyrimidine, as produced at our facility, plays a vital role in multiple downstream industries requiring precise heterocyclic chemistry. Our clients apply this intermediate according to stringent regulatory environments, adapting its use for pharmaceutical ingredients, agricultural chemicals, colorant synthesis, and specialty resin formulations. The following sections detail specific industrial applications, process integration points, compliance, and product types where pyrimidine is essential.

    1. Pharmaceutical APIs Synthesis

    Downstream pharmaceutical manufacturers incorporate pyrimidine as a central building block during active pharmaceutical ingredient (API) development, especially for antivirals, anticancer agents, and cardiovascular drugs. Pyrimidine enters multi-stage synthesis routes, often via nucleophilic substitution or condensation reactions, to yield target therapeutic compounds structured around the pyrimidine ring. Regulatory frameworks in healthcare demand full traceability and validated processes at every batch stage, leading formulators to optimize input ratios based on the specific yield, impurity profile, and subsequent functionalization steps.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practices (APIs)
    • European Pharmacopoeia (Ph. Eur.) monographs referencing synthetic intermediates
    • US FDA 21 CFR Part 210/211 (pharmaceutical manufacturing quality systems)
    • Chinese Pharmacopoeia for small molecule API production

    Typical usage ratio

    • 0.2–1.6 molar equivalents relative to target molecule, adjusted according to desired API substitution pattern or multistep transformations; stoichiometry determined via lab-scale route optimization and scaled to production batch

    Downstream process integration

    • Charged at the nucleophilic aromatic substitution or condensation stage during GMP-compliant reaction scheme; handled in controlled environments to ensure impurity management, with in-line reaction monitoring and isolation for next synthetic step

    Final product types

    • Antiviral nucleoside analogues (e.g., zidovudine precursors)
    • Anticancer APIs (e.g., fluoropyrimidines for solid tumor chemotherapies)
    • Antihypertensive agents (e.g., minoxidil precursors)
    • Various investigational drugs in clinical manufacturing pipelines

    2. Crop Protection and Agrochemical Synthesis

    Leading agrochemical producers utilize pyrimidine core structures to synthesize advanced herbicides and fungicides, leveraging its reactivity in cyclization and alkylation reactions. Custom-formulated intermediates produced from pyrimidine serve as the basis for active crop protection ingredients, supporting stringent environmental and residue regulations. The exact percentage introduced to each formulation typically depends on the conversion efficiency, target molecule complexity, and downstream derivatization yields.

    Industry compliance standards

    • FAO/WHO Specifications for Agricultural Pesticides
    • US EPA 40 CFR Part 180 (pesticide residue regulations)
    • REACH Registration, Evaluation, Authorisation and Restriction of Chemicals (EU)
    • ISO 9001:2015 Certified Quality Management Systems for chemical intermediates

    Typical usage ratio

    • 0.8–2.5 equivalents per target agrochemical molecule; formulated based on downstream functional group tolerance and conversion rate in active ingredient synthesis

    Downstream process integration

    • Fed into the initial heterocyclic construction stage, followed by halogenation, sulfonation, or alkylation to produce target crop protection compounds; process performed in closed reactor systems with downstream purification and formulation

    Final product types

    • Herbicide active ingredients (including pyrimidinyl-ureas)
    • Systemic fungicides (pyrimidine-based or derived compounds)
    • Seed treatment agents for cereal and rice crops
    • Intermediate bulk chemicals for branded agrochemical production

    3. Dye and Pigment Precursor Manufacturing

    Specialty colorant manufacturers integrate pyrimidine into the synthesis of high-performance dyes and pigments, especially for textile coloration and inkjet formulations requiring strong lightfastness and thermal stability. Pyrimidine’s aromatic properties facilitate coupling reactions and complexation, which drive shade intensity and fastness needed for demanding industrial and commercial applications. Regulatory mandates for the sector cover environmental, safety, and end-product use across global markets.

    Industry compliance standards

    • OEKO-TEX® Standard 100 (textile product safety)
    • EU REACH Annex XVII (restrictive substances in colorants)
    • ZDHC MRSL (Zero Discharge of Hazardous Chemicals Manufacturing Restricted Substances List)
    • ISO 1833 for textile color stability testing

    Typical usage ratio

    • 0.1–0.6 molar equivalents per pigment or dye batch, depending on substitution depth and color intensity required by the formulation architecture; proportion varied during pilot scale development for specific shade targets

    Downstream process integration

    • Introduced during the coupling, condensation, or complexation stage in dye synthesis; process follows continuous or batch mode with solvent recycling and final purification to textile-grade specifications

    Final product types

    • Pyrimidine-derived azo dyes for textiles and nonwovens
    • Heat-resistant pigments for automotive and industrial coatings
    • High-chroma inkjet printing colorants
    • Specialty color formulations for plastics compounding

    4. Specialty Polymer and Resin Production

    Industrial polymer manufacturers exploit the reactivity of pyrimidine rings in the synthesis of specialty resins and thermosetting materials for high-performance applications. Incorporation of pyrimidine units into polymer backbones imparts improved chemical and UV resistance, which is essential for protective coatings, aerospace composites, and specialty adhesives. Input ratios are calculated based on desired crosslink density and compatibility with existing polymer matrices, fine-tuned through pilot-scale extrusion and cure cycle validation.

    Industry compliance standards

    • ASTM D256 and D638 (polymer and thermoset mechanical testing)
    • RoHS 2011/65/EU (Restriction of Hazardous Substances)
    • UL 94 (Flammability testing for plastics)
    • ISO 9001:2015 for continuous process monitoring

    Typical usage ratio

    • 0.3–1.2 wt% relative to total resin mass, determined by polymer backbone structure and desired final physical-chemical properties; proportioning adapted according to crosslinking requirements and compatibility assessments

    Downstream process integration

    • Blended at the oligomerization or pre-polymer formation stage, often in the presence of catalysts and co-monomers; followed by controlled polymerization or crosslinking to ensure uniform dispersion and final mechanical performance

    Final product types

    • Weather-resistant industrial coatings (equipment and machinery paints)
    • High-strength aerospace composite resins
    • Specialty adhesives for electronics encapsulation
    • UV-stable plastic additives for technical applications
    Free Quote

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