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Phenyl 1,4-Dihydroxy-2-Naphthoate

    • Product Name Phenyl 1,4-Dihydroxy-2-Naphthoate
    • Alias menadione
    • Einecs 242-383-4
    • 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

    454158

    Chemical Name Phenyl 1,4-Dihydroxy-2-Naphthoate
    Molecular Formula C17H12O4
    Molecular Weight 280.28 g/mol
    Cas Number 2161-85-9
    Appearance Light yellow powder
    Melting Point 190-194 °C
    Solubility Insoluble in water, soluble in organic solvents
    Purity Typically ≥98%
    Storage Conditions Store at 2-8°C, in a dry and well-ventilated place
    Synonyms Phenyl 1,4-dihydroxy-2-naphthalenecarboxylate
    Usage Intermediate in organic synthesis
    Structure Type Aromatic ester

    As an accredited Phenyl 1,4-Dihydroxy-2-Naphthoate 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 25g of Phenyl 1,4-Dihydroxy-2-Naphthoate, tightly sealed with a screw cap and labeled for laboratory use.
    Shipping Phenyl 1,4-Dihydroxy-2-Naphthoate is shipped in tightly sealed containers, protected from light, moisture, and heat. It is classified as a laboratory chemical and must be handled according to safety regulations. Appropriate labeling and documentation are provided, and it is transported by certified carriers strictly following all applicable chemical shipping guidelines.
    Storage Phenyl 1,4-Dihydroxy-2-Naphthoate should be stored in a tightly sealed container, protected from light, heat, and moisture. Keep it in a cool, dry, and well-ventilated area, away from incompatible substances such as strong oxidizers. Always label the container clearly and follow local chemical storage regulations. Personal protective equipment should be used when handling the compound.
    Application of Phenyl 1,4-Dihydroxy-2-Naphthoate

    Applications of Phenyl 1,4-Dihydroxy-2-Naphthoate in Industrial Manufacturing

    Phenyl 1,4-Dihydroxy-2-Naphthoate serves as a specialized intermediate with proven downstream applications in industries requiring stringent performance and compliance with global standards. The following sections outline established industrial use cases, each with defined integration steps, regulatory frameworks, formulation practices, and final product outputs.

    1. High-Performance Colorant Manufacturing for Plastics

    This compound supports the synthesis of specialty naphthalimide dyes and pigments used in high-performance thermoplastic applications. Formulators in this segment value the raw material for its stability in light and heat, as well as its compatibility with both engineering plastics and polyolefins. Consistency in tint strength and purity directly affects final color specifications and regulatory acceptance, requiring strict adherence to validated manufacturing parameters.

    Industry compliance standards

    • EU Regulation (EC) No 1907/2006 (REACH) for pigment composition
    • RoHS Directive 2011/65/EU for electronic equipment plastics
    • EN 71-3: Safety of Toys – Migration of Certain Elements
    • ISO 9001:2015 for pigment quality management systems

    Typical usage ratio

    • 0.1-1.2% by weight of total polymer blend, tailored according to polymer melt point and end-use exposure requirements

    Downstream process integration

    • Dispersed in the pre-polymer blending phase using twin-screw extrusion; added prior to pelletization or direct molding for masterbatch and compounders

    Final product types

    • Color masterbatches
    • Injection-molded automotive interior parts
    • Consumer appliance housings
    • Electrical connector casings

    2. Organic Photoconductor Layer Synthesis in Imaging Drums

    This material provides a key building block for hydroxy-naphthalimide-based photoconductor coatings used in electrophotographic imaging drums. Original Equipment Manufacturers (OEMs) rely on controlled particle size and compatibility with conductive binders, affecting both charge transport properties and operational lifespan in printers and copiers. Batch consistency and trace residue monitoring remain critical to ensure stable photoconductor performance during scaled production.

    Industry compliance standards

    • IEC 62321: Determination of certain substances in electrotechnical products
    • ISO/TC 42: Photography – Sensitized materials
    • REACH SVHC conformity
    • OEM internal QC protocols (per Lexmark, Canon, HP material specifications)

    Typical usage ratio

    • 1.0-4.0% by solids, depending on binder matrix composition and final film thickness targets

    Downstream process integration

    • Integrated during solvent-phase dispersion with binder resins; coated onto aluminum cylinders or sheets through dip-coating and subsequent baking steps

    Final product types

    • Electrophotographic imaging drums
    • Organic photoconductor photoreceptors for printers
    • Copier drum assemblies

    3. Intermediate for Pharmaceutical Dye Synthesis

    Key pharmaceutical dye manufacturers utilize this chemical as a precursor for naphthalimide dyes serving in diagnostic stains and histopathology. Close control over material trace impurities and isoform ratios is enforced to meet pharmacopeial purity demands. The integration point involves high-yield condensation reactions, which directly impact the dye’s spectral properties and its qualification in medical diagnostic kits.

    Industry compliance standards

    • USP/NF (United States Pharmacopeia & National Formulary) for dye intermediates
    • ICH Q3A(R2) for residual solvents and impurities
    • 21 CFR Part 211 for finished pharmaceutical chemicals
    • GMP (Good Manufacturing Practice, EU and US)

    Typical usage ratio

    • 0.5-2.5 equivalents against base molecule in condensation and cyclization reaction steps, optimized for dye yield and purity

    Downstream process integration

    • Charged in initial condensation reaction as principal raw material; followed by controlled crystallization and high-resolution purification for dye separation

    Final product types

    • Medical-grade naphthalimide dyes
    • Diagnostic cytology stains
    • Pathological slide colorants

    4. Fluorescent Marker Synthesis for Polymer Analytics

    Material scientists and polymer manufacturers use this compound to synthesize fluorescent marker molecules, crucial for tracing polymer resin flow and validating dispersion in multilayer films. Analytical laboratories demand assurance of low background contamination and fine control of photochemical reactivity to provide clear fluorescence signals without interfering excipients or byproducts.

    Industry compliance standards

    • ISO 17025: General requirements for the competence of testing and calibration laboratories
    • ASTM D3426: Standard Practice for Fluorescent Filtration Efficiency
    • Analytical validation protocols for trace additives (internal OE-manufacturer specs)

    Typical usage ratio

    • 2–30 ppm by weight in analytical-grade polymer resin, titrated based on detection threshold and film thickness parameters

    Downstream process integration

    • Added to polymer melt prior to extrusion or film casting; post-processing monitored by UV-Vis fluorescence analysis

    Final product types

    • Fluorescent tracer-labeled films
    • Analytical polymer standards
    • Quality control test strips for polymer processing validation

    5. Intermediate for Heat-Stable Coating Resins

    Producers of specialty coating resins rely on this chemical as a monomer for synthesizing high-gloss, lightfast naphthalimide-functionalized resins. These materials satisfy automotive and appliance OEM demands for high-temperature resistance, UV stability, and minimal VOC emission. Control over raw material remains essential to secure consistent reaction kinetics and final resin clarity after polymerization and curing.

    Industry compliance standards

    • EN 13501 (reaction to fire classification)
    • ISO 12944-6 (coating performance for corrosion protection)
    • Automotive manufacturer material specifications (e.g., PSA, GM, VW Technical Delivery Conditions)
    • RoHS Directive for restricted substances

    Typical usage ratio

    • 1.5–6% by mass relative to resin precursor, fine-tuned for resin flow and coating performance properties

    Downstream process integration

    • Integrated in polycondensation reaction kettle; reacted under nitrogen or inert gas at specified temperatures before dilution for coating formulation

    Final product types

    • Automotive exterior and interior coatings
    • High-gloss appliance paints
    • Protective clear coats for industrial equipment
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