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2-Pyrimidinecarboxylic Acid, Methyl Ester

    • Product Name 2-Pyrimidinecarboxylic Acid, Methyl Ester
    • Alias Methyl 2-pyrimidinecarboxylate
    • Einecs 241-396-9
    • 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

    104805

    Name 2-Pyrimidinecarboxylic Acid, Methyl Ester
    Synonyms Methyl 2-pyrimidinecarboxylate
    Cas Number 5780-65-8
    Molecular Formula C6H6N2O2
    Molecular Weight 138.12 g/mol
    Appearance White to off-white crystalline powder
    Melting Point 61-66 °C
    Boiling Point 276.7 °C at 760 mmHg
    Solubility Slightly soluble in water; soluble in organic solvents such as ethanol
    Density 1.278 g/cm3
    Purity Typically ≥98%
    Smiles COC(=O)C1=NC=CN=C1
    Inchi InChI=1S/C6H6N2O2/c1-10-6(9)5-7-3-2-4-8-5/h2-4H,1H3
    Storage Temperature Store at 2-8 °C
    Refractive Index 1.537

    As an accredited 2-Pyrimidinecarboxylic Acid, Methyl Ester factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing A 25-gram bottle of 2-Pyrimidinecarboxylic Acid, Methyl Ester comes in an amber glass vial with tamper-evident cap and hazard labeling.
    Shipping 2-Pyrimidinecarboxylic Acid, Methyl Ester is shipped in secure, tightly sealed containers to prevent exposure to air and moisture. Packaging complies with relevant chemical safety regulations, including labeling with hazard and handling information. Transport is conducted by authorized carriers, ensuring protection from physical damage, extreme temperatures, and contamination during transit.
    Storage 2-Pyrimidinecarboxylic Acid, Methyl Ester should be stored in a tightly closed container, in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizers. Protect the chemical from light and moisture. Ensure proper labeling and handle with appropriate safety precautions, including the use of gloves and eye protection.
    Application of 2-Pyrimidinecarboxylic Acid, Methyl Ester

    Applications of 2-Pyrimidinecarboxylic Acid, Methyl Ester in Industrial Manufacturing

    2-Pyrimidinecarboxylic Acid, Methyl Ester serves as a critical intermediate for several advanced manufacturing sectors. Backed by procedural expertise and compliance with international quality standards, our production supports stringent downstream processing demands across pharmaceuticals, agrochemicals, specialty chemical synthesis, and analytical reference material manufacturing. Each of the following sectors incorporates this raw material according to distinct technical and regulatory requirements.

    1. Pharmaceutical Intermediate Synthesis

    Pharmaceutical manufacturers incorporate this compound as a building block during the assembly of heterocyclic drug molecules, particularly in antiviral and anticancer research pipelines. The material enters key condensation and cyclization reactions required by innovative small-molecule APIs, where purity, trace control, and precursor stability dictate overall process success and batch reproducibility.

    Industry compliance standards

    • ICH Q7 GMP for Active Pharmaceutical Ingredient Production
    • United States Pharmacopeia (USP) General Chapter <795>, <1079>
    • European Pharmacopoeia (Ph. Eur.) monograph compliance for starting materials
    • FDA 21 CFR Part 211 for finished drug production, emphasizing traceability in API supply chains

    Typical usage ratio

    • Dosage may range from 5% to 12% molar equivalent relative to other heterocyclic intermediates, adjusted based on route optimization and target compound structure.

    Downstream process integration

    • Introduced in Stage 2 or 3 of multi-step synthetic pathways; often involved in cyclization or methylation steps after initial ring formation and halogenation.

    Final product types

    • Nucleoside analogue APIs
    • Anti-infective drug molecules for both oral and IV formulations
    • Oncology research compounds entering clinical trial scale-up
    • Advanced pharmaceutical reference standards

    2. Agrochemical Active Ingredient Manufacturing

    Crop protection producers select this ester as a precursor for pyrimidine-based herbicides and fungicides. Its chemical structure enables downstream conversion into active moieties with crop selectivity and resistance management profiles. High batch uniformity and trace impurity control are critical to meeting regulatory standards in different agricultural markets worldwide.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • REACH (EC 1907/2006) registration for chemical substances in European agrochemical supply
    • ISO 9001:2015 Quality Management for chemical manufacturing
    • China GB/T 328.2—2017 for pesticide technical material

    Typical usage ratio

    • Usually dosed at 8–18% by weight as a secondary building block, with adjustments for reaction scale and target derivative yield in active production.

    Downstream process integration

    • Fed into the initial ring functionalization stage or as a selective methylating agent prior to coupling and chlorination steps in bulk actives manufacturing.

    Final product types

    • Pyrimidinyl-based herbicide actives (e.g., components of flumioxazin-type products)
    • Fungicidal seed treatment agents
    • Technical agrochemical intermediates for export registration dossiers
    • Non-systemic foliar active ingredient concentrates

    3. Dye and Pigment Intermediate Processing

    Specialty chemical companies engaged in colorant development utilize this raw material for advanced dye molecule synthesis, especially for high-lightfastness and heat-stable pigments. It enables the formation of stable pyrimidinyl rings within dye chromophores, influencing bathochromic shifts during the final stage of pigment molecule crystallization. Stringent process control maintains high color purity and reproducibility required by industrial textile, ink, and plastic compounding applications.

    Industry compliance standards

    • OEKO-TEX Standard 100 chemical restriction lists for dyes
    • EN 71-3:2019 (Safety of Toys – Migration of certain elements) for pigment use
    • ISO 9001:2015 process conformity for colorant manufacture
    • Textile Ecology Standards relevant to major import/export markets

    Typical usage ratio

    • Normally applied at 2–7% by dry weight of total dye precursor mix, with tunable dosing per desired chromophore intensity and stability specification.

    Downstream process integration

    • Entry at the azo coupling or cyclization phase prior to crystallization and purification; integration into continuous pigment synthesis lines or batch dye reactors.

    Final product types

    • High-purity pigment powders for plastic masterbatches
    • Reactive textile dyes for cellulose and protein fibers
    • Industrial inkjet colorants
    • Specialty printing ink dispersions

    4. Analytical Standards and Reference Material Production

    Reference standard laboratories and analytical chemistry providers demand this chemical for traceable, certified analytical standards used in pharmaceutical and environmental analysis. Reliable batch consistency and ultra-low impurity levels underpin its suitability for the preparation of calibration solutions and assay system controls, including standard mixes for synthetic route validation and toxicological screening.

    Industry compliance standards

    • ISO 17034:2016 for reference material producers
    • ISO/IEC 17025:2017 calibration laboratory requirements
    • USP General Chapter <1224> for reference standards
    • OECD Good Laboratory Practice (GLP) Principles

    Typical usage ratio

    • Employed at 99.5%+ assay (trace impurity <0.1%), with sample size standardized as per certificate of analysis and solution calibration demands (typically 1–10 mg ranges for laboratory standards).

    Downstream process integration

    • Purified and certified during quantitative analysis workflows; introduced at the standard preparation and calibration stages for high-precision chromatographic and spectrometric systems.

    Final product types

    • Pharmaceutical and environmental analytical reference standards
    • Certified calibration solutions for LC, GC, and MS analyses
    • Synthetic route validation kits
    • Proficiency testing materials for regulated laboratories
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