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1-Naphthalenemethylamine

    • Product Name 1-Naphthalenemethylamine
    • Alias 1-(Naphthalen-1-yl)methanamine
    • Einecs 211-829-7
    • 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
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    Specifications

    HS Code

    812310

    Chemical Name 1-Naphthalenemethylamine
    Cas Number 613-03-4
    Molecular Formula C11H11N
    Molecular Weight 157.21 g/mol
    Appearance White to off-white solid
    Melting Point 50-54 °C
    Boiling Point 310 °C
    Density 1.12 g/cm3
    Solubility Slightly soluble in water; soluble in organic solvents
    Smiles c1ccc2cc(ccc2c1)CN
    Inchi InChI=1S/C11H11N/c12-8-10-6-5-7-9-3-1-2-4-11(9)10/h1-7H,8,12H2
    Pubchem Cid 12899

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

    Packing & Storage
    Packing The 1-Naphthalenemethylamine is packaged in a 100-gram amber glass bottle, clearly labeled with chemical name, CAS number, and hazard symbols.
    Shipping 1-Naphthalenemethylamine is shipped in sealed, chemical-resistant containers to prevent leakage and contamination. Packages comply with all relevant safety regulations, including labeling for hazardous materials. The product is protected from moisture, sunlight, and extreme temperatures during transit, and handled by certified carriers to ensure safe and compliant delivery to the recipient.
    Storage 1-Naphthalenemethylamine should be stored in a tightly closed container in a cool, dry, and well-ventilated area, away from incompatible substances such as strong oxidizers and acids. Keep it away from sources of ignition and direct sunlight. Ensure storage is secured and properly labeled, and use secondary containment to prevent leaks or spills. Store at room temperature unless otherwise specified.
    Application of 1-Naphthalenemethylamine

    Applications of 1-Naphthalenemethylamine in Industrial Manufacturing

    As a direct producer, we support global chemical manufacturers with high-purity 1-Naphthalenemethylamine, tailored for well-established downstream industries. The following sectors represent major real-world industrial applications, detailing typical compliance standards, incorporation methods, process positions, and resulting final goods to aid responsible and effective integration of this compound into your workflows.

    1. Agrochemical Intermediate Synthesis

    Leading crop protection producers utilize this amine as a key intermediate for synthesizing advanced heterocyclic herbicides and fungicides. Formulators rely on precise molar equivalents in condensation and alkylation reactions, following national and multinational pesticide regulations for purity and impurity control. Our customers optimize conversion yields and impurity profiles to meet growing regulatory scrutiny and evolving field performance benchmarks demanded by agricultural supply chains.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • REACH Regulation (EC) No 1907/2006
    • ISO 9001:2015 Quality Management
    • US EPA Active Ingredient Registration

    Typical usage ratio

    • Used at 0.85–1.05 molar equivalents relative to the core agrochemical framework; fine-tuned based on target herbicide or fungicide and side-chain substitution requirements

    Downstream process integration

    • Introduced during heterocycle building or aromatic substitution, often as one of the earliest amination steps; participates in batch and flow syntheses requiring strict control of reaction temperature and pH

    Final product types

    • Precursor for triazole-class fungicides
    • Building block for naphthyl-based selective herbicides
    • Intermediate for systemic insecticide synthesis

    2. Dye and Pigment Manufacture

    This aromatic amine enables synthesis of specialty azo, anthraquinone, and phthalocyanine dyes for high-performance textile and ink applications. Carefully controlled amination and coupling steps leverage the molecular structure to achieve colorfastness and shade stability meeting international standards. Manufacturers often choose processing windows, solvent systems, and catalyst loads based on target dye series and downstream application constraints.

    Industry compliance standards

    • OEKO-TEX® Standard 100
    • EU Regulation (EC) No 1907/2006 – REACH Annex XVII (for aromatic amines in textiles)
    • ISO 9001:2015 Quality Management for Dyes
    • EN 71-3:2019 (Safety requirements for colorants in toys)

    Typical usage ratio

    • 0.5–2.0% w/w based on total dye batch; specific loading determined by desired chromophore intensity, solubility, and end-use lightfastness requirements

    Downstream process integration

    • Acts as a primary or auxiliary amine during diazotization and coupling steps in dye synthesis; participates before or after core pigment formation in multiphase colorant production lines

    Final product types

    • Naphthylazo dyes for cotton, wool, and synthetic blends
    • Colorants for industrial coatings and inks
    • High-purity intermediates for pigment dispersions

    3. Pharmaceutical API Intermediate

    GMP-compliant pharmaceutical manufacturers select this compound to build advanced heterocyclic and aromatic frameworks in active pharmaceutical ingredient (API) precursor chains. It enters well-documented synthetic routes where amination, condensation, and N-alkylation must achieve stringent impurity specifications, supporting batch traceability and regulatory submissions under global pharmacopoeias.

    Industry compliance standards

    • ICH Q7A (Good Manufacturing Practice for Active Pharmaceutical Ingredients)
    • 21 CFR Part 211 (US FDA cGMP for finished pharmaceuticals)
    • European Pharmacopoeia (Ph. Eur.)
    • Chinese Pharmacopoeia (ChP)

    Typical usage ratio

    • 0.95–1.10 equivalents by mol in multistep synthesis; adjusted for yield optimization and minimization of side reactions in pilot and commercial API runs

    Downstream process integration

    • Introduced at nucleophilic substitution or amide formation stages; performs as a reaction partner in closed cGMP reactors, with robust QC/QA monitoring throughout the synthetic route

    Final product types

    • API intermediates for oncology and anti-inflammatory drugs
    • Precursors for central nervous system actives
    • Building blocks for cardiovascular medication synthesis

    4. Specialty Polymer Additive Synthesis

    Producers of engineering plastics and specialty resins use this amine to introduce reactive sites into polymer backbones, enhancing material compatibility, adhesion, or electrical properties. The addition protocol depends on polymer type—typically aliphatic or aromatic polyamides, epoxies, or vinyl resins—with strict focus on additive dispersibility and residual monomer limits to maintain compliance and product consistency.

    Industry compliance standards

    • ISO 9001:2015 and ISO 14001:2015 for polymer manufacture
    • REACH Annex XVII – restricted substances
    • UL 94 (plastics flammability standard, if used in electrical applications)
    • RoHS Directive (2011/65/EU) for electronics grade resins

    Typical usage ratio

    • 0.3–1.2% w/w relative to base polymer mass, optimized for desired property modification and cross-linking density while avoiding migration or discoloration

    Downstream process integration

    • Dosed pre-polymerization in melt, suspension, or solution polymerization; may also be grafted post-polymerization in compounding stages under inert conditions to prevent oxidative degradation

    Final product types

    • Modified polyamide engineering plastics for automotive and electronics
    • Reactive intermediates for thermosetting resins
    • Polymer-based adhesive and sealant masterbatches

    5. Organic Electronic Material Synthesis

    Manufacturers producing organic semiconductors and functional coatings value this amine for its ability to modify charge-transport characteristics in small-molecule and polymeric optoelectronic materials. Used in laboratory and pilot-scale OLED, OPV, and OFET manufacturing, strict monitoring for trace metal, residual solvent, and impurity levels supports performance and reliability targets set by device integrators.

    Industry compliance standards

    • IPC-1752A Declarable Substance Requirements
    • IEC 61249-2-21 (halogen-free materials for printed wiring board).
    • ISO 14644-1 (Cleanroom standards for electronics material processing)
    • RoHS Directive (2011/65/EU)

    Typical usage ratio

    • 0.1–0.6 molar equivalents in precursor coupling or modification reactions; exact ratio set according to target HOMO–LUMO levels and device function

    Downstream process integration

    • Enters pre- or post-polymerization modification in organic electronic precursors; fed into glovebox or controlled-atmosphere lines to prevent air/moisture contamination affecting optoelectronic properties

    Final product types

    • OLED emitter and host material intermediates
    • Organic photovoltaic absorber/blend components
    • Small-molecule organic field-effect transistor (OFET) active layers
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