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3-Oxo-3-Thiophen-2-Yl-Propionic Acid Ethyl Ester

    • Product Name 3-Oxo-3-Thiophen-2-Yl-Propionic Acid Ethyl Ester
    • Alias Ethyl 3-oxo-3-(thiophen-2-yl)propanoate
    • Einecs 417-660-2
    • 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

    828878

    Productname 3-Oxo-3-Thiophen-2-Yl-Propionic Acid Ethyl Ester
    Casnumber 888504-28-1
    Molecularformula C9H10O3S
    Molecularweight 198.24
    Appearance Yellow liquid
    Purity ≥97%
    Boilingpoint Unknown
    Density Unknown
    Smiles CCOC(=O)CC(=O)C1=CC=CS1
    Inchikey XODCBBDYXCSXKF-UHFFFAOYSA-N
    Solubility Unknown
    Storagetemperature Store at 2-8°C
    Refractiveindex Unknown
    Synonyms Ethyl 3-oxo-3-(2-thienyl)propanoate

    As an accredited 3-Oxo-3-Thiophen-2-Yl-Propionic Acid Ethyl Ester factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The packaging contains 25 grams of 3-Oxo-3-Thiophen-2-Yl-Propionic Acid Ethyl Ester, securely sealed in an amber glass bottle.
    Shipping **Shipping Description:** 3-Oxo-3-Thiophen-2-Yl-Propionic Acid Ethyl Ester is shipped in tightly sealed, chemically resistant containers to prevent leakage. It must be packaged according to relevant chemical transport regulations, kept away from moisture, extreme temperatures, and incompatible substances. Proper labeling, hazard documentation, and safety data are included to ensure safe and compliant transit.
    Storage 3-Oxo-3-Thiophen-2-Yl-Propionic Acid Ethyl Ester should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from direct sunlight, heat sources, and moisture. Keep away from incompatible substances, such as strong oxidizers and acids. Store at room temperature or as recommended on the label. Ensure appropriate labeling and restrict access to trained personnel.
    Application of 3-Oxo-3-Thiophen-2-Yl-Propionic Acid Ethyl Ester

    Applications of 3-Oxo-3-Thiophen-2-Yl-Propionic Acid Ethyl Ester in Industrial Manufacturing

    As a specialist manufacturer, we supply 3-Oxo-3-Thiophen-2-Yl-Propionic Acid Ethyl Ester to leading formulators serving the pharmaceutical intermediate, agrochemical synthesis, specialty polymer, and organic electronic materials industries. Based on field-validated processes, we detail specific downstream scenarios in which this advanced thiophene-based building block is indispensable.

    1. Pharmaceutical Intermediate for Thienopyridine Synthesis

    Our material plays a critical role as a key intermediate in synthesizing thienopyridine scaffolds used in cardiovascular therapeutic agents. Downstream pharmaceutical manufacturers deploy it specifically during the construction of thiophene-fused heterocycles, leveraging its controlled reactivity in acylation and ring-closure steps. The ester group offers convenient deprotection, tailoring the process for high-purity API requirements.

    Industry compliance standards

    • ICH Q7 (Good Manufacturing Practice for APIs)
    • Ph. Eur. (European Pharmacopoeia, relevant monographs)
    • 21 CFR Part 211 (FDA cGMP for Finished Pharmaceuticals)
    • USP General Chapters on impurities & solvent residues

    Typical usage ratio

    • 0.6 – 1.2 molar equivalents based on targeted yield, adjusted per process stoichiometry

    Downstream process integration

    • Introduction at the heterocycle building stage, following condensation of the nucleophile and prior to ring fusion step
    • In-line monitoring of ester conversion and impurity profiles; usage often involves parallel purification units

    Final product types

    • Thienopyridine drug substance (intermediate stage)
    • Active pharmaceutical ingredient (e.g., antiplatelet agent precursors)

    2. Agrochemical Precursor for Heterocyclic Fungicides

    This compound is incorporated by agrochemical producers as a selective building block in the preparation of thiophene-containing fungicidal actives. Its functionalization enables precise substitution, giving rise to molecules with enhanced soil mobility and pathogen resistance. Manufacturers achieve reliable scale-ups while meeting regulatory traceability and impurity controls specific to global crop protection.

    Industry compliance standards

    • ISO 9001:2015 (Quality Management Systems)
    • FAO/WHO Joint Meeting on Pesticide Specifications (JMPS)
    • REACH Annex VII-XI (for registration of agrochemical intermediates in EU)

    Typical usage ratio

    • 8–12% by mass of total formulation in active crop protection synthesis, adjusted by desired thiophene substitution pattern

    Downstream process integration

    • Direct charging into multi-step batch reactors during the heteroatom substitution or oxidation phase
    • Formulation blending post-synthesis for granule or suspension concentrate production

    Final product types

    • Heterocyclic fungicide active ingredient
    • Seed treatment and foliar spray premixes

    3. Specialty Polymer Additive for Conductive Resins

    In the field of advanced materials, manufacturers select this ester as a chain-modifying co-monomer during the synthesis of polythiophene derivatives designed for antistatic and ESD control applications. Its incorporation modulates resin rheology, conductivity, and film integrity, serving fabrication partners producing regulatory-compliant components for electronics enclosures and specialty coatings industries.

    Industry compliance standards

    • RoHS 3 (Directive 2015/863/EU, hazardous substances in electronics)
    • IEC 61340-5-1/2 (Electrostatic discharge control)
    • UL 94 (Flammability safety standard for plastic materials)

    Typical usage ratio

    • 1.0–4.5% by mass in copolymer feeds, titrated via conductivity target and mechanical property requirements

    Downstream process integration

    • Fed into polymerization reactor as minor co-monomer during in-situ chain-growth of thiophene-based copolymers
    • Post-polymerization blending for compound modification ahead of extrusion or film-casting line

    Final product types

    • ESD (Electrostatic Discharge) protective housings
    • Anti-static packaging films
    • Printed electronic substrates

    4. Organic Electronics: Precursor for OLED and OPV Materials

    Producers engaged in organic electronics integrate this ester in the synthesis of electron-donating blocks for OLED emissive layers and organic photovoltaic active blends. Its structural motif fine-tunes charge transport and solubility characteristics, thereby optimizing the electroluminescent and photovoltaic layer properties required for high-performance electronic devices.

    Industry compliance standards

    • IEC 62341 (OLED display devices)
    • ISO 9001:2015 (applied to electronic material manufacturing)
    • Restriction of Hazardous Substances (RoHS) compliance for device assemblies

    Typical usage ratio

    • 0.2–1.0% by active layer formulation weight, adjusted based on emission/absorption targets in device design

    Downstream process integration

    • Chemical introduction in organic synthesis stage for multi-ring electron donor construction
    • Blending and solution processing preceding casting or spin-coating of active device layers

    Final product types

    • OLED panel organic emitters
    • Organic photovoltaic absorber materials
    • OPV module active layers
    Free Quote

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