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Ethyl Acetamidocyanoacetate

    • Product Name Ethyl Acetamidocyanoacetate
    • Alias EAACA
    • Einecs 'EINECS 401-590-5'
    • 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

    234912

    Chemical Name Ethyl Acetamidocyanoacetate
    Molecular Formula C7H10N2O3
    Molar Mass 170.17 g/mol
    Cas Number 36247-62-6
    Appearance White to off-white solid
    Melting Point 82-86°C
    Solubility Soluble in common organic solvents
    Boiling Point Decomposes
    Density 1.25 g/cm3 (estimated)
    Storage Conditions Store at room temperature, away from moisture and light

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

    Packing & Storage
    Packing 500g of Ethyl Acetamidocyanoacetate is packaged in a sealed, amber glass bottle with a secure screw cap and clear labeling.
    Shipping Ethyl Acetamidocyanoacetate should be shipped in tightly sealed, chemical-resistant containers, protected from moisture and direct sunlight. It must be labeled according to relevant hazardous material regulations. During transport, maintain ambient temperature, avoid physical damage, and comply with any applicable local, national, or international shipping and safety guidelines for chemicals.
    Storage Ethyl Acetamidocyanoacetate should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from sources of ignition, heat, and incompatible materials such as strong acids and bases. Protect from moisture and direct sunlight. Use proper labeling and safety precautions, and store at room temperature unless otherwise specified by the manufacturer or safety data sheet (SDS).
    Application of Ethyl Acetamidocyanoacetate

    Applications of Ethyl Acetamidocyanoacetate in Industrial Manufacturing

    As an established manufacturer of Ethyl Acetamidocyanoacetate, we serve a select range of chemical synthesis sectors where this intermediate plays a critical role. Below we outline its core applications in downstream industries, specifying the relevant compliance standards, use levels, manufacturing integration points, and the types of final products supported by our raw material.

    1. Pharmaceutical Intermediate for Pyrimidine and Thymine Base Synthesis

    In the pharmaceutical sector, Ethyl Acetamidocyanoacetate is utilized as a critical building block during the manufacture of nucleobase derivatives such as substituted pyrimidines and thymine analogues. These compounds contribute to the synthesis of various nucleoside drugs and are especially significant in the development of several antiviral and oncology medications. Rigorous GMP practices regulate this production environment, requiring close control over raw material quality, batch documentation, and traceability starting from the introduction of the intermediate during the condensation and subsequent cyclization steps in the route to nucleobase synthesis. Final active pharmaceutical ingredients (APIs) benefit from the molecular specificity afforded by properly integrated raw materials.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice (GMP) for Active Pharmaceutical Ingredients
    • Ph. Eur. (European Pharmacopoeia) monographs for nucleobase and nucleoside derivatives
    • US FDA 21 CFR Part 211 (cGMP for Finished Pharmaceuticals)

    Typical usage ratio

    • Reactant load typically 0.8–1.1 molar equivalents relative to aldehyde or amine partners; adjusted based on yield and product purity requirements in scale-up synthesis

    Downstream process integration

    • Added during early condensation reactions, followed by controlled cyclization, purification, and crystallization steps under GMP monitoring

    Final product types

    • Nucleoside antiviral agents (e.g., intermediate for zidovudine synthesis)
    • Cytostatic drugs utilizing pyrimidine or thymine scaffolds

    2. Agrochemical Intermediate for Herbicide Synthesis

    In agrochemical manufacturing, this cyanoacetate compound functions as a cornerstone intermediate for selective herbicides based on pyrimidinone and triazine structures. Facilities producing these actives must operate according to international quality and environmental standards, ensuring each batch conforms to agrochemical regulatory dossiers before downstream formulation. The material typically enters the process during the heterocyclic ring construction, where its amide and nitrile functionalities enable efficient linkage, thereby supporting the production of high-purity active ingredients for market-ready crop protection agents.

    Industry compliance standards

    • ISO 9001:2015 (Quality Management System for Agrochemical Production)
    • FAO/WHO Codex Alimentarius – Pesticide Residue Standards
    • REACH Regulation (EC) No 1907/2006 for intermediates

    Typical usage ratio

    • 5–12% by weight of total reaction mass in initial ring-synthesis stage, subject to active ingredient yield optimization and waste minimization targets

    Downstream process integration

    • Dosed at the ring-forming condensation step, undergoes sequential coupling, isolation, and formulation into technical concentrate under ISO and FAO guidelines

    Final product types

    • Technical grade herbicide actives (e.g. pyrimidinone-based compounds)
    • Preformulated herbicide concentrates for field application

    3. Dye and Pigment Intermediate for Specialty Organic Pigments

    Specialty pigment manufacturers employ this raw material as a core intermediate for synthesizing heterocyclic azo dyes and high-performance organic pigments. The compound's amidocyano functionalization grants precise control over chromophore formation, which is crucial in high-value applications such as high-color-fastness printing inks and coatings. The process usually incorporates it during key cyclization and coupling steps before pigment isolation, purification, and dispersing. Consistency in input ratios and batch traceability is mandated by compliance certifications related to environmental impact and product safety, with all finished pigment products tested for residual intermediates and compliance with allowed substance lists.

    Industry compliance standards

    • EN 71-3 (European Toy Safety for Pigments in Printing Inks)
    • ISO 9001:2015 for pigment quality system control
    • REACH SVHC compliance for aromatic amine release

    Typical usage ratio

    • 3–8% by weight of chromophore-forming stage, with specific ratio determined according to desired shade intensity and pigment crystal morphology

    Downstream process integration

    • Added as a precursor in the cyclization or diazotization stages, followed by pigment precipitation, washing, and micronization

    Final product types

    • High-performance organic pigments for printing inks
    • Color dispersions for plastics and synthetic fibers

    4. Intermediate for Fine Chemical Synthesis in Specialty Resins

    This material also fills a specialist niche as a precursor for the synthesis of heterocycle-modified monomers used in high-performance resins. Manufacturers in this arena focus on advanced polymeric materials for electronic encapsulation, adhesives, or high-durability coatings. Production must follow strict controls in line with electronic material regulations to ensure consistency of dielectric or mechanical properties in the resulting resins. Integration occurs at the monomer synthesis stage, utilizing the acetamidocyano functional group for custom cyclization reactions, subsequently enabling development of electrically insulating or chemically resistant resin products.

    Industry compliance standards

    • IPC-4101 (Specification for Base Materials for Printed Circuits)
    • RoHS Directive 2011/65/EU (Restriction of Hazardous Substances in Electrical/Electronic Equipment)
    • ISO 14001:2015 (Environmental Management in Resin Manufacturing)

    Typical usage ratio

    • 2–6% by weight during targeted monomer synthesis, tailored upward for higher crosslink density or heat resistance based on end-use requirements

    Downstream process integration

    • Inserted during controlled cycloaddition reactions before subsequent resinification and curing operations

    Final product types

    • High-performance resin monomers for electronic encapsulants
    • Specialty adhesives for industrial electrical assembly
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