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1-Benzofuran-3-Ylacetonitrile

    • Product Name 1-Benzofuran-3-Ylacetonitrile
    • Alias 3-(1-Benzofuran-3-yl)acetonitrile
    • Einecs 246-913-9
    • 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

    557220

    Chemical Name 1-Benzofuran-3-ylacetonitrile
    Molecular Formula C10H7NO
    Molecular Weight 157.17 g/mol
    Cas Number 4969-54-8
    Appearance White to off-white solid
    Melting Point 72-76 °C
    Solubility Soluble in organic solvents such as DMSO and methanol
    Purity Typically ≥97%
    Smiles N#CCc1coc2ccccc12
    Inchi InChI=1S/C10H7NO/c11-7-6-9-8-12-10-5-3-1-2-4-10(9)10

    As an accredited 1-Benzofuran-3-Ylacetonitrile factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Brown glass bottle, 25g quantity, tightly sealed with tamper-evident cap, labeled with chemical name, formula, and hazard warnings.
    Shipping **Shipping Description for 1-Benzofuran-3-ylacetonitrile:** This chemical is typically shipped in tightly sealed containers under inert gas, away from moisture and light, conforming to all applicable regulations. It should be labeled as a laboratory chemical, handled with care, and packaged to prevent breakage during transit, with proper documentation and hazard identification if required.
    Storage 1-Benzofuran-3-ylacetonitrile should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from sources of ignition, heat, and incompatible substances such as strong oxidizers. Protect from moisture and direct sunlight. Ensure proper labeling, and access should be restricted to trained personnel. Adhere to all appropriate safety and regulatory guidelines for chemical storage.
    Application of 1-Benzofuran-3-Ylacetonitrile

    Applications of 1-Benzofuran-3-Ylacetonitrile in Industrial Manufacturing

    As a direct manufacturer of 1-Benzofuran-3-Ylacetonitrile, we supply this specialty intermediate to industry leaders across key sectors demanding stringent compliance and formulation consistency. Our team provides technical support to help downstream clients optimize yields and maintain control over formulation parameters at scale. The following sections present in-depth information on the principal industrial applications, process stages, and relevant usage ranges within established global markets.

    1. Pharmaceutical Intermediate for Anti-arrhythmic Agents

    Pharmaceutical companies use 1-Benzofuran-3-Ylacetonitrile primarily in the synthesis of benzo-fused heterocyclic compounds as core intermediates for anti-arrhythmic active pharmaceutical ingredients (APIs). Downstream API manufacturers integrate this ingredient into precise synthesis steps, subject to regular audits and rigorous process validation under global medicinal product regulations. Our supply chain and batch traceability ensure that each delivery aligns with current Good Manufacturing Practice (cGMP) and full analytical support.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP, EP, and JP Pharmacopoeial impurity requirements
    • US FDA 21 CFR Parts 210/211
    • EU GMP Directive 2003/94/EC

    Typical usage ratio

    • 0.1 – 0.4 molar equivalents; the precise ratio varies depending on target API and synthesis scale, with process development optimization based on stoichiometric efficiency and impurity profiles.

    Downstream process integration

    • Charged to early or mid-stage condensation or nucleophilic addition reactions during heterocycle construction, often followed by reductive or further cyclization steps in multipurpose reactors.

    Final product types

    • Class III anti-arrhythmic drug substances (APIs)
    • Benzo[b]furan pharmaceutical building blocks
    • Finished oral and parenteral anti-arrhythmic medicines

    2. Advanced Agrochemical Synthesis

    Leading agrochemical producers employ 1-Benzofuran-3-Ylacetonitrile as a functionalized intermediate for new-generation fungicides and insecticides, focusing on selective mode-of-action chemistry with minimal environmental residue. The downstream process integrates this specialty nitrile into tailored synthetic pathways that comply closely with pesticide formulation regulatory reviews and extended pilot-scale validations.

    Industry compliance standards

    • FAO/WHO Codex Alimentarius for pesticide ingredients
    • EU Regulation (EC) No 1107/2009 – Plant Protection Products
    • China GB/T 1604 – Synthetic Pesticide Quality
    • ISO 9001 audited quality management for technical materials

    Typical usage ratio

    • 2.5 – 5.0% by weight of precursor mix in multi-step syntheses; adjusted through process research based on crop application spectrum and residue limits.

    Downstream process integration

    • Incorporated during early-stage functionalization or coupling reactions in the synthesis of benzofuran-based bioactive scaffolds for subsequent formulation as technical concentrates.

    Final product types

    • Systemic fungicide technical concentrates
    • Insecticide active ingredient intermediates
    • Final formulated agricultural chemical products (WP, EC, SC formats)

    3. Specialty Dye and Pigment Intermediates

    Manufacturers of high-performance dyes engineer 1-Benzofuran-3-Ylacetonitrile into proprietary pigment molecules, especially for benzofuran-based colorants used in advanced textile processing, plastics coloration, and inkjet ink applications. The ingredient's role centers on building chromophore frameworks via controlled coupling and condensation steps to achieve durable color fastness and resistance profiles required by demanding end-use certification systems.

    Industry compliance standards

    • Oeko-Tex Standard 100 – Harmful Substance Test Certification
    • REACH Regulation (EC) No 1907/2006 — Registration, Evaluation, Authorisation and Restriction of Chemicals
    • ISO 105 Series – Color Fastness of Textiles
    • ZDHC MRSL (Manufacturing Restricted Substances List)

    Typical usage ratio

    • 0.5 – 2.5% of total reactive intermediate batch mass; process engineers optimize based on desired shade intensity, thermal stability, and substrate application.

    Downstream process integration

    • Added as a key building block in batchwise or continuous synthesis for the preparation of benzofuran-based azo or anthraquinone dye intermediates in dedicated reactors.

    Final product types

    • Textile reactive dyes for cellulosic fiber finishing
    • High-stability pigments for engineering plastics
    • Industrial inkjet printing inks

    4. Organic Electronic and Photonic Material Precursors

    Producers in the organic electronics sector utilize this benzofuran derivative in the custom synthesis of small-molecule organic semiconductors and photonic materials. The process, executed under cleanroom and electronics-grade environments, emphasizes electronic structure fine-tuning and chain extension required for next-generation emissive layers and photoconductive devices.

    Industry compliance standards

    • JEITA EIAJ ED-4701 – Environmental Test Methods for Electronic Components
    • IPC-4101 – Specification for Base Materials for Printed Boards
    • RoHS Directive 2011/65/EU (Restriction of Hazardous Substances)
    • ISO 14001 Environmental Management

    Typical usage ratio

    • 0.2 – 1.2% of monomer feed, balanced according to desired film thickness, carrier mobility, and optical purity requirements of the targeted device.

    Downstream process integration

    • Fed into monomer coupling and chain-growth polymerization steps for precursor resin synthesis and molecular engineering in functional materials R&D and pilot production lines.

    Final product types

    • OLED (Organic Light Emitting Diode) emissive materials
    • Organic photovoltaic prepolymers
    • Photoconductive thin-film device layers
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