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2-Phenylindole-3-Carboxaldehyde

    • Product Name 2-Phenylindole-3-Carboxaldehyde
    • Alias 2-Phenyl-1H-indole-3-carbaldehyde
    • Einecs 629-087-6
    • 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

    167414

    Chemical Name 2-Phenylindole-3-Carboxaldehyde
    Molecular Formula C15H11NO
    Molecular Weight 221.26 g/mol
    Cas Number 26250-36-4
    Appearance Off-white to light yellow solid
    Melting Point 178-180 °C
    Purity Typically >98%
    Solubility Soluble in organic solvents (e.g., DMSO, ethanol)
    Storage Conditions Store at 2-8°C, protected from light and moisture
    Synonyms 2-Phenyl-1H-indole-3-carboxaldehyde
    Inchi Key RQUIZXIGNZZKEX-UHFFFAOYSA-N
    Smiles C1=CC=C(C=C1)C2=NC=C(C3=CC=CC=C32)C=O

    As an accredited 2-Phenylindole-3-Carboxaldehyde factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle containing 5 grams of 2-Phenylindole-3-carboxaldehyde, sealed with a screw cap, labeled with hazard information.
    Shipping 2-Phenylindole-3-Carboxaldehyde is shipped in compliance with chemical safety regulations. The compound is securely packed in sealed containers and cushioned packaging to prevent leaks or breakage. Shipping is typically via ground or air freight, labeled as a research chemical, with all relevant hazard and handling documentation included to ensure safe transport.
    Storage Store 2-Phenylindole-3-Carboxaldehyde in a tightly sealed container, protected from light and moisture. Keep in a cool, dry, and well-ventilated area, away from incompatible substances, including strong oxidizers. Label the container clearly and avoid exposure to air for extended periods. Use appropriate personal protective equipment when handling, and follow local regulations for chemical storage and disposal.
    Application of 2-Phenylindole-3-Carboxaldehyde

    Applications of 2-Phenylindole-3-Carboxaldehyde in Industrial Manufacturing

    2-Phenylindole-3-Carboxaldehyde is an advanced indole derivative, primarily used as an intermediate in high-value chemical syntheses. Our production supports key sectors such as pharmaceuticals, dyes, fine chemicals, and advanced materials, where precise compliance, repeatable formulations, and integration into specialized downstream processes are essential for consistent final product quality.

    1. Pharmaceutical Active Pharmaceutical Ingredient (API) Synthesis

    Our 2-Phenylindole-3-Carboxaldehyde serves as a core building block for heterocyclic core modification in oncology and CNS drug API development. Downstream formulators incorporate this material into route design for selective indole-based active moieties, especially in late-stage functionalization, where regulated impurity profiles and detailed reaction parameter control are critical. Strict traceability, solvent handling protocols, and phase-purity checks support compliance and regulatory filings.

    Industry compliance standards

    • ICH Q7 GMP Guideline for API Manufacture
    • US FDA 21 CFR 211
    • EU EMA Guidelines for Starting Materials
    • Chinese Pharmacopoeia (for domestic filing)

    Typical usage ratio

    • 3–12% w/w in indole API intermediate step, adjusted according to target yield and purification pathway

    Downstream process integration

    • Introduced at acylation or condensation stage, often via controlled batch addition to avoid side-chain isomerization; enters directly into multi-step synthesis leading to drug substance endpoint

    Final product types

    • Targeted oncology APIs (e.g., indole kinase inhibitors)
    • CNS disorder drug substances
    • Clinical candidate reference standards for regulatory submission
    • Advanced intermediates for pilot-scale cGMP manufacture

    2. Specialty Dye Intermediates

    The molecule facilitates introduction of chromophore structures in high-performance dye manufacturing, specifically in the production of novel indole-based colorants used in textiles and specialty printing inks. Strict color purity, substantial batch reproducibility, and compatibility with sulfonation/metallization stages are critical during downstream processing. Consistent aldehyde reactivity supports the stability of downstream pigment synthesis in regulated industries.

    Industry compliance standards

    • EU REACH Registration for Dye Intermediates
    • Oeko-Tex Standard 100 (for textile applicability)
    • ZDHC MRSL (chemical input quality)
    • ISO 9001-2015 (quality management systems in pigment processing)

    Typical usage ratio

    • 5–18% as a precursor in batch dye synthesis; actual ratio adjusted based on required colorimetric strength and shade stability

    Downstream process integration

    • Fed at nucleophilic addition stage for chromophore ring construction; reacts during coupling or condensation before sulfonation/metallization and post-processing purification

    Final product types

    • Textile disperse dyes (shade-specific indole variants)
    • Specialty digital printing inks (UV-resistant formulations)
    • Solvent-stable pigment dispersions
    • Organic pigment lakes for plastics coloration

    3. Fine Chemical Synthesis for Agrochemical Building Blocks

    Factories use 2-Phenylindole-3-Carboxaldehyde as an advanced platform intermediate for the development of agrochemical active ingredients including plant growth regulators and fungicide scaffolds. Stringent process documentation, raw material traceability, and controlled reaction scale-up ensure regulatory acceptance and downstream fit into multi-step fine chemical campaigns.

    Industry compliance standards

    • FAO/WHO JMPR pesticide specification protocols
    • ISO 17025 quality system in analytical process control
    • Directive 91/414/EEC for agrochemical active substances
    • China GB 2763 standards on crop protection inputs

    Typical usage ratio

    • Typically 4–10% w/w in intermediate stage, modulated for process economy and downstream coupling efficiency

    Downstream process integration

    • Added during nucleophilic aromatic substitution or cyclization step; directly feeds into bulk synthesis of key agrochemical intermediates prior to functional group modification

    Final product types

    • Plant growth regulation agents with indole moieties
    • Fungicide intermediates for seed treatment
    • Indole-based herbicide scaffolds
    • Pre-formulated crop protection blends

    4. Organic Electronics and OLED Material Development

    Researchers and production engineers leverage this material for synthesis of indole-based organic semiconductors and charge transport materials in OLED and organic photovoltaic device manufacturing. Careful purity documentation, batch reproducibility, and controlled crystallinity contribute to robust electronic performance. Tightly controlled aldehyde incorporation impacts emissive efficiency and device lifetime in next-generation material platforms.

    Industry compliance standards

    • RoHS Directive 2011/65/EU for electronics inputs
    • IEC 62321 (hazardous substance content control)
    • ISO 14001 Environmental Management during electronics-grade chemical prep
    • Cleanroom GMP for OLED module raw materials (ISO 14644-1)

    Typical usage ratio

    • Usage varies from 2–7% by mass in batch monomer formation for charge-transport layers—scale depends on substrate architecture and target molecular weight

    Downstream process integration

    • Integrated in initial monomer synthesis before polymerization, or used in late-stage side-chain modification for fine-tuning optical bandgap and solubility

    Final product types

    • OLED hole-transport materials
    • Indole-based blue emitter molecules
    • Thin-film semiconducting polymers
    • Multi-layer organic optoelectronic devices
    Free Quote

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