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2-Naphthonitrile

    • Product Name 2-Naphthonitrile
    • Alias 2-Cyanonaphthalene
    • Einecs 205-863-9
    • 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

    125540

    Chemical Name 2-Naphthonitrile
    Cas Number 581-89-5
    Molecular Formula C11H7N
    Molecular Weight 153.18 g/mol
    Appearance White to yellow crystalline powder
    Melting Point 56-59°C
    Boiling Point 305-307°C
    Density 1.19 g/cm³
    Solubility In Water Insoluble
    Flash Point 129°C
    Refractive Index 1.670
    Smiles C1=CC=C2C=CC=CC2=C1C#N

    As an accredited 2-Naphthonitrile 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 100 grams of 2-Naphthonitrile; features a secure screw cap and detailed hazard labeling for safe handling.
    Shipping 2-Naphthonitrile is shipped in tightly sealed containers, typically made of glass or high-density polyethylene, to prevent leaks and contamination. It must be stored in a cool, dry, well-ventilated area, away from incompatible substances. Proper labeling, hazard identification, and compliance with local transport regulations are essential during shipping.
    Storage 2-Naphthonitrile should be stored in a cool, dry, and well-ventilated area, away from sources of ignition and direct sunlight. Keep the container tightly closed and protected from moisture. Store separately from incompatible materials such as strong oxidizers and acids. Use appropriate, labeled chemical storage containers. Ensure access to proper spill containment and emergency equipment in the storage area.
    Application of 2-Naphthonitrile

    Applications of 2-Naphthonitrile in Industrial Manufacturing

    2-Naphthonitrile plays a fundamental role as an intermediate in several advanced industrial applications, serving as a building block in the synthesis of specialty compounds, engineered dyes, pharmaceutical actives, and performance materials. Its use depends on precise process integration, adherence to sector-specific regulations, and custom formulation according to the requirements of downstream manufacturers.

    1. Synthesis of Agrochemical Intermediates

    Many agrochemical producers employ 2-naphthonitrile as a key intermediate for crafting selective herbicides and insecticides. Manufacturers convert it through controlled amination or hydrolysis into functionalized naphthyl compounds. Stringent process control is necessary during nitrile group transformation to ensure purity, as downstream active ingredients must meet strict residue and migration standards for agricultural compounds.

    Industry compliance standards

    • FAO/WHO Specifications and Evaluations for Agricultural Pesticides
    • European Regulation (EC) No 1107/2009 for Plant Protection Products
    • US EPA FIFRA Registration Requirements
    • ISO 17025 Quality Management for Chemical Analysis

    Typical usage ratio

    • 10–25% of total batch mass, adjusted based on targeted intermediate yield and process selectivity.

    Downstream process integration

    • Added during the early condensation or cyclization step in herbicide and insecticide core synthesis lines.

    Final product types

    • Selective herbicide active ingredients (e.g., naphthylcarboxamide class)
    • Insecticide precursor molecules with naphthalene moiety
    • Pesticide intermediates used in API registration dossiers
    • Raw material for agricultural adjuvant production

    2. Manufacture of Azo and Anthraquinone Dyes

    Dye manufacturers rely on 2-naphthonitrile during the synthesis of high-performance azo and anthraquinone pigments. Its chemical structure facilitates diazotization and coupling reactions, resulting in intense, lightfast shades used across textile, printing, and plastics industries. Handling and formulation must satisfy colorant purity criteria, with attention to minimizing aromatic impurities and maintaining batch consistency for color performance.

    Industry compliance standards

    • OEKO-TEX Standard 100 (Textile Safety)
    • EN 71-3 (Migration of Certain Elements - Toy Safety)
    • REACH Annex XVII (Restriction on Certain Azo Compounds)
    • ISO 9001 Quality Management for Colorant Production

    Typical usage ratio

    • 15–30% by mol in dye intermediate synthesis, dependent on desired chromophore formation and reactivity of couplers.

    Downstream process integration

    • Introduced during coupling step after diazotization to build naphthyl-based color intermediates.

    Final product types

    • Reactive and direct textile dyes (navy blue, black, red series)
    • Anthraquinone pigment intermediates for plastics
    • Solvent dyes for ink and coatings
    • Sulfonated dye derivatives for paper coloration

    3. Advanced Pharmaceutical Intermediate Synthesis

    API and contract manufacturers utilize 2-naphthonitrile as a nucleus in the synthesis of pharmaceutical intermediates, especially where naphthalene derivatives form an active core. Its application demands high-purity grades and validated process controls. It undergoes condensation, reduction, and cyclization to generate pharmacophores for antipsychotic, anti-inflammatory, and kinase inhibitor drug classes under cGMP environments.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practices for Active Pharmaceutical Ingredients
    • USP/NF Monographs for Pharmaceutical Intermediates
    • EDQM CEP/COS Dossier Requirements
    • 21 CFR Parts 210–211 (US FDA cGMP Regulations)

    Typical usage ratio

    • 5–18% by weight in pharmaceutical intermediate synthesis; process route and yield requirements set final ratio.

    Downstream process integration

    • Charged at early API intermediate building step; subjected to multi-step transformations such as nitrile reduction and aromatic substitution during GMP production.

    Final product types

    • API intermediates for quinoline and benzothiazole drugs
    • Active end-compounds for CNS and oncology medications
    • Fine chemicals for medicinal research synthesis
    • Pharmacopeial reference standards containing naphthalene motifs

    4. Production of Liquid Crystal Materials

    Producers of advanced electronic materials incorporate 2-naphthonitrile derivatives as core units in the synthesis of nematic and smectic liquid crystal compounds. The high conjugation and rigid structure support the formation of ordered phases for display applications. Rigorous purification and conformance to electronics-grade material standards are essential, as downstream performance hinges on molecular alignment and thermal stability in finished liquid crystal displays (LCDs).

    Industry compliance standards

    • RoHS Directive 2011/65/EU (Restriction of Hazardous Substances in Electronics)
    • JEITA Standards for Electronic Materials
    • IEC 60454-3-1 (Electronic Assembly Specifications)
    • ISO 14001 Environmental Management for Electronics Manufacturing

    Typical usage ratio

    • 8–22% on molecular composition basis within custom-formulated liquid crystal blends, depending on target refractive index and dielectric anisotropy.

    Downstream process integration

    • Introduced at oligomerization stage followed by purification and isomer separation. Final formulation occurs prior to cell encapsulation in display module assembly.

    Final product types

    • Nematic and smectic liquid crystal mixtures for TFT-LCD panels
    • OLED alignment layer additives
    • Precursor materials for electronic paper displays
    • Advanced matrix addressable display substrates

    5. Synthesis of High-Performance Polymers

    In specialty polymer applications, 2-naphthonitrile serves as a monomer for producing high glass-transition temperature (Tg) resins and naphthalene-based engineering plastics. The nitrile group provides sites for functional polymerization and cyclization, yielding materials with enhanced chemical resistance and mechanical strength. Strict input quality and process traceability are mandatory, especially where the plastics target electronic, transport, or industrial equipment markets.

    Industry compliance standards

    • UL 94 (Flammability Standard for Plastics)
    • ASTM D638 (Standard Test for Tensile Properties of Plastics)
    • ISO 9001 Quality Management for Polymer Manufacturing
    • REACH Regulation (EC) No 1907/2006 (Polymer Safety)

    Typical usage ratio

    • 12–28% by weight in monomer charge, varied by the degree of polymer backbone substitution required.

    Downstream process integration

    • Fed into polymerization reactors as a functionalized monomer; chain-growth or step-growth reactions subsequently amplify the molecular structure.

    Final product types

    • Naphthalene-based polyesters and polyimides
    • Chemical-resistant engineering plastics
    • High-performance resin adhesives
    • Specialty copolymers for electronic and industrial applications
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