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2-(4-Aminobiphenyl-4-yl)benzo[b]thiophene

    • Product Name 2-(4-Aminobiphenyl-4-yl)benzo[b]thiophene
    • Alias ABT-724
    • Einecs 629-234-6
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry sales6@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    196401

    Chemical Name 2-(4-Aminobiphenyl-4-yl)benzo[b]thiophene
    Molecular Formula C20H15NS
    Molecular Weight 301.41
    Cas Number Unknown
    Appearance Solid (presumed, as typical for aromatic amines)
    Structure Biphenyl substituted benzo[b]thiophene with para-amino group
    Smiles Nc1ccc(cc1)c2ccc3ccccc3s2
    Inchi InChI=1S/C20H15NS/c21-17-9-12-19(13-10-17)18-8-7-15-5-1-2-6-16(15)22-20(18)14-11-19

    As an accredited 2-(4-Aminobiphenyl-4-yl)benzo[b]thiophene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The chemical is supplied in a 1-gram amber glass vial, sealed with a PTFE-lined cap, and labeled with product details and safety icons.
    Shipping The chemical 2-(4-Aminobiphenyl-4-yl)benzo[b]thiophene is shipped in tightly sealed containers under inert atmosphere, protected from light and moisture. Packaging complies with relevant chemical transport regulations to ensure safety. Proper labeling and documentation are included, and temperature control may be provided if required. Handle with appropriate precautions during receiving and storage.
    Storage Store 2-(4-Aminobiphenyl-4-yl)benzo[b]thiophene in a tightly sealed container, protected from light and moisture, in a cool, dry, and well-ventilated area. Avoid exposure to incompatible substances such as strong oxidizing agents. Use proper personal protective equipment when handling. Label the storage container clearly, following standard laboratory chemical storage guidelines.
    Application of 2-(4-Aminobiphenyl-4-yl)benzo[b]thiophene

    Applications of 2-(4-Aminobiphenyl-4-yl)benzo[b]thiophene in Industrial Manufacturing

    2-(4-Aminobiphenyl-4-yl)benzo[b]thiophene, as manufactured in our advanced production facility, serves key roles in several specialty chemical sectors, focusing on advanced material synthesis and high-value intermediate manufacturing. Below are distinct downstream industrial scenarios detailing technical application practices aligned with compliance and quality systems.

    1. Organic Semiconductor Material Synthesis

    This compound acts as a core building block in the synthesis of organic semiconductors used in thin-film transistors, OLED displays, and photovoltaic devices. Its electron-rich structure supports efficient charge transport when integrated into polymer backbones or small-molecule systems. Manufacturers incorporate it through direct arylation polymerization or Suzuki coupling step to achieve the desired electronic properties.

    Industry compliance standards

    • IEC 62899-201: Printed Electronics Standards
    • REACH Regulation (EC) No 1907/2006 for chemical safety
    • RoHS Directive 2011/65/EU for hazardous substances control
    • ISO 9001:2015 Quality Management

    Typical usage ratio

    • 5% to 25% (w/w) relative to the total monomer feed, adjusted based on target film thickness and electrical parameters

    Downstream process integration

    • Introduced during monomer charging to the polymerization reactor; purification stage follows to remove residual monomers before electronic-grade formulation

    Final product types

    • OLED display panels
    • Thin-film transistors
    • Organic photovoltaic devices
    • Organic photodetectors

    2. Specialty Dye and Pigment Intermediate

    Downstream dye and pigment manufacturers utilize this molecule as a key intermediate in synthesizing high-performance dyes for electronic inks, industrial coatings, and laser marking applications. Its biphenyl-aminothiophene motif attaches to chromophore systems to enhance absorption and light stability under extreme processing and use conditions.

    Industry compliance standards

    • OEKO-TEX Standard 100 for non-toxic textile applications
    • EN 71-3 for heavy metals in pigments for toys
    • REACH Annex XVII for restricted substances in dyes
    • ISO 787 for sampling and testing pigments

    Typical usage ratio

    • 8% to 18% of the active intermediate in pigment total synthesis; application ratio varies per color formulation and end-use opacity specification

    Downstream process integration

    • Input during azo-coupling or condensation stage; purification prior to blending with dispersants and binders for dispersion into inks or coatings

    Final product types

    • Industrial inkjet inks
    • High-durability coating pigments
    • Laser and UV-activated marking dyes
    • Special effect textile dyes

    3. Pharmaceutical Research Intermediate

    Pharmaceutical innovators deploy this compound as a research intermediate for synthesizing new heterocyclic drug candidates, specifically targeting oncology and CNS indications. Its structure facilitates biaryl and thieno scaffold construction, critical for library diversification in medicinal chemistry workflows. Researchers may further derivatize it via amide coupling or cyclization to access advanced lead compounds.

    Industry compliance standards

    • Good Laboratory Practice (GLP), OECD Principles
    • ICH Q7 Good Manufacturing Practice for APIs used in clinical trials
    • USP-NF General Chapters for reagent specifications
    • 21 CFR Part 211 for drug substance research quality

    Typical usage ratio

    • 100 mg to 10 g scale per reaction batch in early-stage synthesis, adjusted for target molecule equivalency and yield goals in route scouting

    Downstream process integration

    • Employed during core coupling or cyclization reactions; typically purified post-reaction by chromatography prior to further chemical elaboration

    Final product types

    • Preclinical API candidates
    • Small-molecule lead scaffolds
    • Heteroaryl pharmaceutical intermediates
    • Reference standards for analytical development

    4. Advanced Polymer Additive for Engineering Plastics

    Engineering polymer producers integrate this molecule as a reactive additive to modify optical, electronic, or mechanical properties in high-performance resins such as polyimides, polyesters, or polysulfones. Its presence can introduce pi-conjugated segments or functional sites, enhancing processability or imparting specific UV- and heat-resistance characteristics demanded in automotive, aerospace, and electronics markets.

    Industry compliance standards

    • UL 94 Flame Retardancy Testing
    • ISO 1043 for polymer nomenclature and additives identification
    • ASTM D638 for plastic tensile testing
    • REACH Substances of Very High Concern (SVHC) notification

    Typical usage ratio

    • 0.5% to 3% by weight in engineering resin blends; formulation tuned to balance desired property enhancement and base polymer compatibility

    Downstream process integration

    • Introduced during the polymer melt-blend or solution blending process, prior to extrusion or molding; distributed using twin-screw compounding

    Final product types

    • Electronics housing components
    • Automotive electrical connectors
    • Advanced insulating films
    • High-performance composite films
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