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2,5-Dimethoxynaphthalene

    • Product Name 2,5-Dimethoxynaphthalene
    • Alias 2,5-Dimethoxy-naphthalene
    • Einecs 217-543-8
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry sales7@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    868401

    Name 2,5-Dimethoxynaphthalene
    Molecular Formula C12H12O2
    Molecular Weight 188.22 g/mol
    Cas Number 571-58-4
    Appearance White to light yellow solid
    Melting Point 111-114 °C
    Boiling Point 338.3 °C at 760 mmHg
    Density 1.17 g/cm3
    Solubility Slightly soluble in water
    Smiles COC1=CC2=C(C=C1)C=CC(=C2)OC
    Pubchem Cid 12071
    Refractive Index 1.653

    As an accredited 2,5-Dimethoxynaphthalene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 25g 2,5-Dimethoxynaphthalene is supplied in a sealed amber glass bottle with a secure screw cap and hazard labeling.
    Shipping 2,5-Dimethoxynaphthalene is shipped in tightly sealed containers, protected from moisture and light. It should be handled with care, using gloves and goggles. Store in a cool, dry, and well-ventilated area. Ensure containers are clearly labeled and comply with local transport regulations for chemicals. Avoid contact with oxidizing agents.
    Storage 2,5-Dimethoxynaphthalene should be stored in a tightly sealed container in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizers. Protect it from moisture and light. Label the storage container clearly, and ensure proper chemical safety protocols are followed to prevent leaks, exposure, and environmental release.
    Application of 2,5-Dimethoxynaphthalene

    Applications of 2,5-Dimethoxynaphthalene in Industrial Manufacturing

    2,5-Dimethoxynaphthalene serves as a critical intermediate for specialized sectors in the chemical industry. Our production follows stringent controls for purity and traceability, supporting downstream manufacturers that require consistent quality for regulated and technical end uses. Below are primary industrial application areas verified by ongoing demand from formulators and processors.

    1. Pharmaceutical Intermediates for API Synthesis

    Downstream pharmaceutical manufacturers rely on 2,5-dimethoxynaphthalene as a key intermediate for synthesizing high-value active pharmaceutical ingredients (APIs), including anti-tumor and anti-infective agents. The material's aromatic methoxyl groups enable selective functionalization, often as a starting substrate for Suzuki, Buchwald–Hartwig, or Friedel–Crafts reactions. Quality control testing (HPLC, GC-MS) supports batch release to ensure impurity levels suitable for API precursor production.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP & EP intermediate quality requirements
    • 21 CFR Part 210/211 (US FDA finished pharmaceuticals)
    • ISO 9001:2015 Quality Management Systems

    Typical usage ratio

    • Intermediate loading at 0.4–1.2 molar equivalents per reaction, adjusted for target molecule pathway, yield, and impurity profile.

    Downstream process integration

    • Charged as the primary substrate in aromatic substitution and heterocyclic coupling steps.
    • Reacts under Pd/C or Ni catalyst systems in closed, validated reactor lines.
    • QC sampling taken post-coupling before conversion to final API.
    • Captured for recovery or solvent-assist purification before next stage synthesis.

    Final product types

    • Synthetic anti-cancer drugs (e.g., selected kinase inhibitors)
    • Anti-infective and antifungal agents (naphthyl-based cores)
    • Specialty fine chemicals and pilot-scale clinical candidates
    • Registered pharmaceutical intermediates with DMF support

    2. Organic Electronic Materials

    Manufacturers of organic electronic components use 2,5-dimethoxynaphthalene as an essential building block for developing advanced materials in organic light-emitting diodes (OLEDs) and organic photovoltaic (OPV) devices. The compound’s structure enables efficient energy transfer and molecular stacking in emissive layers. Downstream formulators employ precise purification and re-crystallization protocols to achieve batch uniformity, maintaining critical optical and electrical properties required by electronics OEMs.

    Industry compliance standards

    • RoHS Directive (EU 2011/65/EU) for restricted substances
    • REACH (EC 1907/2006) registration for raw materials
    • IEC 62321 for hazardous material testing in electronics
    • ISO 14001:2015 Environmental Management Systems for plant production

    Typical usage ratio

    • Dosed at 3–8% weight basis in polymer blends for OLED or OPV layers; ratio adjusted to meet film formation, mobility, and emission efficiency targets.

    Downstream process integration

    • Introduced during organic synthesis of emitter or charge transport molecules
    • Recrystallized and vacuum-dried prior to thin film fabrication or spin coating
    • Subjected to inline quality analysis for purity, particle size, and residual solvent control
    • Transferred to cleanroom integration under solvent and temperature management

    Final product types

    • OLED panel organic emitter materials
    • Organic semiconductors for flexible displays
    • Photoactive coatings for solar cell absorbers
    • Encapsulated OPV modules for specialty electronics

    3. Agrochemical Synthesis Intermediates

    Producers of specialty pesticides and agricultural fungicides incorporate this intermediate in the synthesis of novel naphthalene-based compounds. Substitution patterns allow for selective chlorination, sulfonation, or coupling to generate bioactive molecules targeting crop protection needs. Purity and isomeric control must be validated by in-house analytical chemistry teams to meet downstream registrant requirements and label claim integrity.

    Industry compliance standards

    • FAO/WHO pesticide specifications for technical materials
    • OECD guidelines for chemical synthesis and characterization
    • GLP (Good Laboratory Practice) for residue studies and traceability
    • ISO 17025 accredited laboratory testing

    Typical usage ratio

    • 0.7–1.4 equivalents relative to main reactant in multi-stage synthesis, frequently adjusted based on targeted biological activity and yield optimization.

    Downstream process integration

    • Added to reaction kettle for halogenation or alkylation
    • Coupled under controlled temperature for active ingredient formation
    • Intermediates isolated and validated for structure by NMR or GC-MS
    • Finished technical concentrate purified for downstream formulation

    Final product types

    • Naphthalene-derived fungicide actives (e.g., crop protection agents)
    • Precursors for seed-treatment compounds
    • Intermediates for regulated herbicides
    • Novel pesticide R&D samples for field testing

    4. Dyes and Pigments Manufacturing

    Leading colorant manufacturers use 2,5-dimethoxynaphthalene for synthesizing naphthyl-based dyes, including permanent azo and solvent dyes focused on industrial coatings, plastics, and specialty inks. The controlled methoxy substitution allows reliable diazotization, coupling, or hydrolysis pathways, delivering intense chromophores with defined shade properties. Production protocols specify high-purity material with no interfering isomers, and product batches undergo rigorous batch traceability from raw material receipt through to pigment isolation.

    Industry compliance standards

    • EN 71-3 Safety of Toys standard for heavy metal content in colorants
    • REACH Annex XVII for restricted dye substances
    • ISO 9001/14001 for pigment production processes
    • AP(89)1 European Resolution on colorants in plastics and coatings

    Typical usage ratio

    • Utilized at 5–20% weight basis in core dye synthesis, adjusted by molar stoichiometry and intended performance attribute (hue strength, solubility, migration)

    Downstream process integration

    • Introduced during the initial diazotization or condensation reactions
    • Filtered and purified via solvent extraction, precipitation, or crystallization
    • Chromatic evaluation and stability testing performed pre-shipment
    • Supplied in pigment dispersions or as finished dye powder

    Final product types

    • Industrial solvent dyes for plastics processing
    • Azo dye intermediates for textile coloration
    • Permanent pigments for automotive or coil coatings
    • Inkjet and specialty ink colorants for high-end applications
    Free Quote

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    Email: sales7@sinochem-nanjing.com

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