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4-Methoxy-1-Naphthol

    • Product Name 4-Methoxy-1-Naphthol
    • Alias 4-Methoxy-1-naphthalenol
    • Einecs 220-969-8
    • 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

    762392

    Cas Number 529-98-4
    Molecular Formula C11H10O2
    Molecular Weight 174.20 g/mol
    Iupac Name 4-Methoxynaphthalen-1-ol
    Appearance Light brown to beige crystalline powder
    Melting Point 132-135 °C
    Boiling Point 354.6 °C at 760 mmHg
    Density 1.19 g/cm³
    Solubility In Water Slightly soluble
    Synonyms 1-Hydroxy-4-methoxynaphthalene
    Refractive Index 1.686
    Pubchem Cid 71243

    As an accredited 4-Methoxy-1-Naphthol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle, 25g, with secure screw cap; white label displays chemical name, CAS number, hazard symbols, and supplier details.
    Shipping 4-Methoxy-1-Naphthol is shipped in tightly sealed containers, protected from light and moisture. The chemical is packaged following standard safety regulations for hazardous materials, using leak-proof glass or plastic bottles and secondary protective packing. Handle and transport in accordance with applicable local, national, and international chemical safety guidelines.
    Storage 4-Methoxy-1-Naphthol should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from direct sunlight and sources of ignition. Keep it separate from strong oxidizing agents and acids. Store at room temperature and avoid exposure to moisture. Properly label containers and ensure access is restricted to trained personnel using appropriate protective equipment.
    Application of 4-Methoxy-1-Naphthol

    Applications of 4-Methoxy-1-Naphthol in Industrial Manufacturing

    As a direct manufacturer of 4-Methoxy-1-Naphthol, we supply this specialty intermediate to leading global industrial partners. Below, we detail primary application areas with operational guidance for downstream producers and OEMs.

    1. Synthesis of Naphtholic Azo Dyes for Textile Printing

    Our material serves as a coupling component in the synthesis of specific azo dyes used for vibrant cotton, viscose, and blended fabric printing. Manufacturers incorporate it during shade preparation, enabling controlled color development through diazotization and coupling reactions. Efficient handling, precision in dosing, and batch traceability remain vital, especially where deep red and maroon shades with high wash fastness are required.

    Industry compliance standards

    • OEKO-TEX Standard 100 (Class I, II requirements for restricted amines)
    • ZDHC MRSL compliance for input chemicals
    • REACH Regulation (EC) No 1907/2006 Annex XVII
    • DIN EN ISO 105 (ISO 105-X12 for color fastness testing)

    Typical usage ratio

    • 0.5% to 2.0% by weight of total dye formulation, adjusted based on target depth and cloth weight
    • Proportion varies with coupler structure and auxiliaries

    Downstream process integration

    • Added to aqueous or solvent phase during in-situ azo dye coupling step
    • Brief stirring and pH adjustment (5–7.5) until coupling completes
    • Used at laboratory or production scale in open or closed reactors

    Final product types

    • Reactive and direct azo dyes in granular or powder form
    • Ready-to-use printing pastes for rotary and screen printing machines
    • Textile printing inks with certified color fastness claims

    2. Intermediate for Antioxidant Additives in Polymer Stabilization

    Producers of specialty antioxidants employ this raw material as a key precursor during the multistep synthesis of naphthol-based stabilizers designed for polyolefin and PVC compounding. Product purity and batch homogeneity directly impact the finished stabilizer's ability to prevent thermal and UV-induced degradation in demanding plastic processing applications.

    Industry compliance standards

    • ISO 9001:2015 for quality management of additive manufacture
    • EU Directive 2011/10/EU on plastic materials intended for food contact (where applied)
    • FDA 21 CFR 177.1520 (for indirect food contact compliance in the US)
    • ASTM D3895 for oxidative induction time (OIT) in polyolefins

    Typical usage ratio

    • 0.05% to 0.5% by polymer weight as part of multi-component stabilizer systems
    • Ratio depends on base polymer, processing temperature, and exposure conditions

    Downstream process integration

    • Used during the condensed phase synthesis of hindered phenolic antioxidants
    • Introduced at the nucleophilic substitution or condensation step prior to final purification
    • QC monitored for trace byproducts and color development

    Final product types

    • Hindered phenolic and secondary aromatic antioxidant additives
    • Stabilizer masterbatches for film, injection molding, and wire/cable insulation
    • Food-grade plastic packaging materials (where compliance achieved)

    3. Precursor for Naphtholic Pharmaceutical Intermediates

    Pharmaceutical API manufacturers integrate this compound as a building block for naphthol-ether skeletal structures, especially in the synthesis of select antineoplastic and anti-inflammatory intermediates. Stringent quality control at every synthesis stage ensures suitability for regulated markets. On-site analytical verification for identity and impurity profiles is compulsory throughout production.

    Industry compliance standards

    • European Pharmacopeia (Ph. Eur.) relevant monographs
    • Current Good Manufacturing Practice (cGMP, ICH Q7)
    • USP <823> for radiopharmaceutical precursors when applicable
    • ISO 17025 for analytical testing laboratories

    Typical usage ratio

    • Varies from 1 mol equivalent up to 1.5 depending on target API synthesis path
    • Adjustment based on yield optimization and impurity management

    Downstream process integration

    • Charged into etherification or Friedel–Crafts acylation steps in controlled reactors
    • Reacts under inert atmosphere to limit oxidative side reactions
    • Lot-wise tracking essential for pharmaceutical regulatory submission

    Final product types

    • Intermediates for non-steroidal anti-inflammatory drugs (NSAIDs)
    • Naphtholic moiety-containing cytostatics or contrast media intermediates
    • Active pharmaceutical ingredient (API) precursors with validated composition

    4. Component for Specialty Pigments in Industrial Coatings

    Advanced pigment manufacturers utilize this compound during the tailor-made synthesis of naphthol pigments, targeting high-performance coatings for automotive and industrial applications. Consistent coloring strength, resistance to solvent extraction, and dispersion stability are key evaluation criteria.

    Industry compliance standards

    • ISO 1248 for general-purpose pigments – physicochemical properties
    • ASTM D4449 (pigment specifications for industrial coatings)
    • Automotive OEM specification sheets (e.g., VW, GM, Ford internal paint standards)
    • REACH pre-registration status required in the EU

    Typical usage ratio

    • Typically 10% to 30% by total pigment synthesis batch
    • Volume adjusted based on the desired hue intensity and particle size distribution

    Downstream process integration

    • Added to the initial condensation step during pigment core formation
    • Reacts under controlled heat and solvent conditions with metal salt modifiers
    • Subsequent filtration, washing, and drying define final pigment qualities

    Final product types

    • High-performance naphthol red and maroon pigments
    • Coating dispersions for automotive topcoat and refinish applications
    • Industrial decorative powder coatings and heat-resistant finishes

    5. Material for Special Paper Chemicals Manufacturing

    Producers of functionalized paper and security documents use this material as a precursor in the preparation of water-soluble dyes and paper surface treatment agents, where high purity and low metal content are strictly monitored. Specialized applications include colored papers, safety certificates, and non-reproducible document solutions.

    Industry compliance standards

    • EN 646 (color fastness to water for paper and board)
    • ISO 187 (conditioning of paper and board samples)
    • FSC CoC certification for sustainable paper sources (as applicable)
    • National Banknote Security Printing requirements (for security documents)

    Typical usage ratio

    • Between 0.2% and 1.0% of total chemical additive blend
    • Ratio selected by target paper shade and end-use specifications

    Downstream process integration

    • Incorporated during paper coating formulation or as part of dyeing solution for wet end or surface size press
    • Monitored for migration and light fastness during production trials
    • Consistency checked against reference standards in each batch

    Final product types

    • Banknote and security document papers
    • Colored digital printing papers for high-fidelity applications
    • Specialty coated arts and crafts papers, event tickets

    6. Raw Material for Analytical Reagent Production

    Laboratory reagent manufacturers prefer this ingredient for the synthesis of chromogenic reagents and analytical colorants requiring high selectivity in metal ion detection. Batch-to-batch reproducibility, microbiological purity, and defined trace impurity levels govern the usability of each supplied lot in certified reagent manufacture.

    Industry compliance standards

    • ISO 6353-1 (Reagents for chemical analysis — Part 1)
    • ASTM E288 for purity of analytical reagents
    • Good Laboratory Practice (GLP) assurance for reagent production
    • Certificate of Analysis (CoA) traceability requirements

    Typical usage ratio

    • 5–20 mmol/L in final analytical formulation, at concentrations optimized for detection limits and color yield
    • Further adjusted based on solution stability and assay requirements

    Downstream process integration

    • Dissolved and reacted to form chelating or colorimetric analytical agents
    • Used in titration mix preparation and trace metal test kits
    • Stability against oxidation ensured by inert packaging and storage

    Final product types

    • Certified laboratory reagents for water, soil, and food analysis
    • Colorimetric and spectrophotometric test kits
    • Trace element detection kits for industrial and research laboratories
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