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6-(4-Fluorophenyl)Indole

    • Product Name 6-(4-Fluorophenyl)Indole
    • Alias 4-Fluoro-6-phenylindole
    • Einecs 629-912-8
    • 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

    711411

    Chemical Name 6-(4-Fluorophenyl)indole
    Molecular Formula C14H10FN
    Molecular Weight 211.24 g/mol
    Cas Number 350-13-4
    Appearance Off-white to pale yellow solid
    Melting Point 132-134°C
    Solubility Slightly soluble in organic solvents
    Smiles c1cc(F)ccc1-c2ccc3ccccc3n2
    Inchikey PLTNMCJMCINOSD-UHFFFAOYSA-N

    As an accredited 6-(4-Fluorophenyl)Indole factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The chemical is packaged in a 10-gram amber glass bottle with a secure cap, labeled with compound name, purity, and hazard warnings.
    Shipping 6-(4-Fluorophenyl)Indole is shipped in a tightly sealed, inert container to prevent moisture and contamination. The package is clearly labeled and handled under standard chemical shipping regulations, often requiring temperature control and protection from light. Proper documentation and compliance with safety guidelines ensure secure and legal transport.
    Storage 6-(4-Fluorophenyl)indole should be stored in a tightly sealed container, kept in a cool, dry, and well-ventilated area away from direct sunlight and incompatible substances such as strong oxidizing agents. Store at room temperature and protect from moisture. Properly label the container, and ensure that only trained personnel handle and access the chemical. Follow all applicable safety guidelines.
    Application of 6-(4-Fluorophenyl)Indole

    Applications of 6-(4-Fluorophenyl)Indole in Industrial Manufacturing

    6-(4-Fluorophenyl)Indole is an essential intermediate for specific high-value downstream sectors. We produce this raw material to meet the process, compliance, and formulation needs of regulated chemical manufacturing. Below, we detail its core industrial application fields, each with segment-specific standards, dosage specifics, process roles, and ultimate product types.

    1. Pharmaceutical Active Pharmaceutical Ingredient (API) Synthesis

    Pharmaceutical producers employ 6-(4-Fluorophenyl)Indole as a core building block in the synthesis of indole-based APIs, notably in development of innovative CNS-active compounds and certain targeted oncology drugs. This raw material’s purity and consistent profile are essential for scalable production under regulated environments, enabling the controlled synthesis through direct coupling and late-stage fluorination steps. Its use is strictly limited to R&D and commercial pipeline compounds under regional drug authority oversight.

    Industry compliance standards

    • ICH Q7 GMP for Active Pharmaceutical Ingredients
    • USP, EP, and JP raw material monograph controls (as applicable per project and customer)
    • 21 CFR Parts 210/211 (USA GMP)
    • EMA guidelines on synthesis starting materials

    Typical usage ratio

    • Used at 1.2–2.5 mole equivalents relative to limiting intermediate in API synthesis route; adjustment depends on route yield and impurity management

    Downstream process integration

    • Introduced during early to mid-stage fragment assembly
    • Participates in Suzuki or Buchwald–Hartwig coupling
    • Subjected to halogen-lithium exchange and directed metallation
    • Critical for achieving final scaffold diversification

    Final product types

    • NCE (new chemical entity) APIs for clinical trials
    • Small-molecule drugs in late-phase pharmaceutical pipeline
    • Reference standards for regulatory submission
    • Pharmacologically active indole derivatives for preclinical evaluation

    2. Agrochemical R&D Intermediate

    Crop protection and agrochemical R&D facilities use this indole as an intermediate in synthesizing prototype fungicides and insecticides, especially where fluorinated pharmacophores improve target specificity and metabolic stability. Our material supports lead generation and structure-activity optimization in academic-industry consortia and internal innovation platforms, where regulatory documentation and traceable batch management are required.

    Industry compliance standards

    • OECD GLP for chemical synthesis (pilot and field trial phases)
    • SANCO/221/2000 (EU pesticide data requirements)
    • ISO 17025 for analytical support and batch traceability
    • REACH (if placed on the EU market for non-exempted uses)

    Typical usage ratio

    • 0.8–1.5 molar equivalents based on target scaffold, tailored to route design and crop protection trial requirements

    Downstream process integration

    • Employed in heterocyclic assembly via indole ring fusion methods
    • Used in fluorination/methylation/alkylation optimization programs
    • Participates in late-stage diversification before biological screening
    • Tested for environmental metabolite tracking

    Final product types

    • Novel fungicide lead compounds (pre-registration)
    • Fluorinated insecticide research samples
    • Reference metabolites for residue analysis
    • Seed treatment chemical intermediates

    3. Specialty Dye and Pigment Precursor

    Advanced dye manufacturers rely on 6-(4-Fluorophenyl)Indole for the production of indole-based pigments, which deliver strong color fastness and enhanced chemical resistance in demanding textile and plastic substrates. Use centers on specialty colorants where the fluorinated aromatic ring improves photostability, processability, and compatibility with high-performance polymers and fibers. Strict documentation and product consistency support both industrial trial and commercial dye blend applications.

    Industry compliance standards

    • EN 71-3 (toy safety requirements for colorants)
    • ISO 105-X12 (textile color fastness methods)
    • OEKO-TEX® Standard 100 for restricted chemicals
    • RSL compliance (branded apparel and technical textiles)

    Typical usage ratio

    • 0.3–1.1 molar equivalents in pigment condensation steps; dosage optimized by shade depth and final fabric/film properties

    Downstream process integration

    • Condensed with aromatic aldehydes via Friedel-Crafts or Mannich quinone methods
    • Precursor for indole-based chromophores in polymer-dye copolymers
    • Incorporated during masterbatch pigment dispersion
    • Subject to fine particle surface engineering for high dispersion stability

    Final product types

    • Azo-indole colorants for plastics and fibers
    • Fluorinated specialty textile dyes
    • Infrared-absorbent pigments for technical fabrics
    • Durable automotive and industrial coatings pigments

    4. Organic Electronics Research Material

    Leading universities and electronics R&D labs order this intermediate for the synthesis of electron-rich materials, especially in the design of new organic semiconductors and light-emitting diodes (OLEDs). Indole-based compounds contribute to improved charge transfer, stability, and device lifetime when incorporated into fluorinated π-conjugated systems. Our controlled synthesis route and batch-specific documentation facilitate reproducibility for optoelectronic materials specialists.

    Industry compliance standards

    • IEC 62321 (RoHS-related restrictions for electronics)
    • ISO/TS 80004-13 (nanotechnology terminology where relevant)
    • University and institutional chemical management policies
    • MSDS and hazardous transport compliance (IATA, IMDG)

    Typical usage ratio

    • 0.25–0.7 molar equivalents in step-growth polymerization or small-molecule OLED dopant synthesis; adjusted during device optimization

    Downstream process integration

    • Used in Pd-catalyzed cross-coupling reactions for donor–acceptor motif creation
    • Integrated in monomer feed for conjugated polymer chain extension
    • Applied as precursor for thin-film spin coating in device prototyping
    • Tested for electronic purity and film-formation properties in QC labs

    Final product types

    • Organic semiconductors for OFET research
    • Prototype OLED emitter and transport materials
    • Solution-processable electronic inks
    • Advanced sensing films for laboratory diagnostics
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