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3-Thiophenezoic Acid

    • Product Name 3-Thiophenezoic Acid
    • Alias 3-Thiophenecarboxylic acid
    • Einecs 242-429-2
    • 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

    174063

    Chemical Name 3-Thiophenezoic Acid
    Molecular Formula C5H4O2S
    Molecular Weight 128.15 g/mol
    Cas Number 41052-97-1
    Appearance White to off-white solid
    Melting Point 124-127 °C
    Solubility In Water Slightly soluble
    Smiles C1=CSC=C1C(=O)O
    Inchi InChI=1S/C5H4O2S/c6-5(7)4-1-2-8-3-4/h1-3H,(H,6,7)
    Storage Conditions Store in a cool, dry place
    Synonyms Thiophene-3-carboxylic acid
    Pka 3.7

    As an accredited 3-Thiophenezoic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 3-Thiophenezoic Acid, 25g: Supplied in an amber glass bottle with secure cap, labeled with product details, safety, and handling instructions.
    Shipping 3-Thiophenezoic Acid is typically shipped as a solid chemical in tightly sealed containers to prevent moisture ingress and contamination. It is transported according to relevant chemical safety and regulatory guidelines, often requiring labeling as a laboratory reagent. Handle with appropriate protective measures and store in a cool, dry, and well-ventilated area during transit.
    Storage 3-Thiophenezoic Acid 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, direct sunlight, and sources of ignition. Always label the container clearly and follow standard chemical handling and storage protocols to ensure safety and stability of the compound.
    Application of 3-Thiophenezoic Acid

    Applications of 3-Thiophenezoic Acid in Industrial Manufacturing

    As a direct manufacturer specializing in heterocyclic intermediates, we supply 3-Thiophenezoic Acid for multiple advanced manufacturing sectors. The following industrial applications reflect actual downstream uses, detailing technical integration, compliance parameters, and real-world dosage requirements in each relevant value chain.

    1. Active Pharmaceutical Ingredient (API) Synthesis for Antithrombotic Drugs

    API manufacturers use 3-Thiophenezoic Acid as a core building block in the synthesis of select antithrombotic agents, leveraging its thiophene ring to introduce bioactivity into the target molecule. The compound enters during late-stage functionalization steps and supports structure-activity relationship (SAR) optimization according to medicinal chemistry protocols. Its specific use is subject to strict regulatory controls, and the addition rate varies depending on the desired final molecular configuration.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice (GMP) for Active Pharmaceutical Ingredients
    • ChP (Chinese Pharmacopoeia) API monograph references
    • FDA 21 CFR Part 210/211 (Current Good Manufacturing Practice)
    • EU GMP Volume 4, Part II for APIs

    Typical usage ratio

    • 0.3–1.8 molar equivalents relative to target API intermediate; chemists adjust equivalents based on the coupling efficiency and functional group conversion rates determined through process development.

    Downstream process integration

    • Introduced during heteroaryl acylation or direct coupling with amine-capped scaffolds in the multi-step synthesis route; typically added at the third or fourth from last step within a closed reaction vessel under inert gas.

    Final product types

    • Bulk crystalline antithrombotic drug intermediate
    • Formulated finished dosage forms such as tablets and injectables (where allowed by local regulations after full downstream synthesis and purification)

    2. Organic Semiconductors for OLED Display Manufacturing

    3-Thiophenezoic Acid serves as a monomer precursor for thiophene-based semiconductor polymers used in organic light-emitting diode (OLED) display substrates. Electronic materials companies utilize its reactive carboxy group to introduce solubilizing side chains or extend π-conjugation, improving charge transport within the polymer film. Its controlled use is critical to maintaining batch consistency and device performance specifications.

    Industry compliance standards

    • IEC 61249-2-21 (Halogen-free materials for electronic substrates)
    • RoHS Directive 2011/65/EU (Restriction of Hazardous Substances in electrical/electronic equipment)
    • Company-specific purity and trace metal specifications
    • ISO 9001:2015 Quality Management System for manufacturing

    Typical usage ratio

    • 5–15% by weight in monomer feed for oxidative polymerization or Suzuki coupling; material scientists optimize the loading depending on target polymer film morphology and device requirements.

    Downstream process integration

    • Introduced during monomer functionalization followed by polymerization, either through batch synthesis or continuous flow; purification involves reprecipitation and column chromatography before application in spin-coating or vapor deposition processes.

    Final product types

    • Organic semiconducting layers in OLED display backplanes
    • Flexible display films and organic thin-film transistors (OTFTs)

    3. Photovoltaic Material Additive in Dye-Sensitized Solar Cells (DSSCs)

    Manufacturers of advanced solar panels apply 3-Thiophenezoic Acid as a modification agent in the synthesis of thiophene-based sensitizers or as a linker for ruthenium complexes, aimed at improving electron injection and stability in DSSCs. Its integration enhances both dye anchoring on TiO2 surfaces and overall device conversion efficiency, subject to rigorous environmental and chemical safety standards in energy materials manufacturing.

    Industry compliance standards

    • IEC 61215:2016 (Design qualification and type approval for crystalline photovoltaic modules)
    • REACH Regulation (EC) No 1907/2006
    • ISO 14001:2015 Environmental Management
    • Internal specifications for solvent and heavy metal residues per photovoltaic industry guidelines

    Typical usage ratio

    • 2–8% by weight in solid or dissolved dye formulation; the amount calibrated based on electrochemical performance results, determined by initial cell assembly test batches.

    Downstream process integration

    • Added during dye molecule synthesis or immediately prior to dye-adsorption step on nanoporous TiO2 electrodes; solvent casting or immersion techniques ensure homogeneous coverage and device repeatability.

    Final product types

    • Dye-sensitized photovoltaic cells and modules
    • Flexible BIPV (Building Integrated Photovoltaic) laminate sheets

    4. Intermediate for Agrochemical Synthesis—Herbicide Development

    Leading crop protection companies incorporate 3-Thiophenezoic Acid into the synthesis of specific heterocyclic herbicide intermediates, where the thiophene framework provides the basis for selectivity and metabolic stability in the final active ingredient. The material enables process chemists to access complex molecular architectures in modern herbicide pipelines while maintaining compliance with agrochemical manufacturing directives.

    Industry compliance standards

    • FAO/WHO Guidelines on Good Manufacturing Practice (GMP) for Pesticide Production
    • ISO 9001:2015 for Quality Systems in agrochemical plants
    • Regulation (EC) No 1107/2009 (EU approval of plant protection products)
    • China National Standard GB 4839-2020 for pesticide technical material production

    Typical usage ratio

    • 1.5–3.5% by weight in the multi-step synthesis of heterocyclic herbicide intermediates; adjusted in accordance with downstream reactivity and impurity profile control during scale-up synthesis.

    Downstream process integration

    • Engaged during cyclization and carboxyl functionalization of precursor molecules; intermediate is isolated, purified, and conveyed to further derivatization and formulation stages in batch or semi-continuous reactors.

    Final product types

    • Technical concentrate herbicide intermediates
    • Formulated crop protection products for field application
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