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3-Hydroxy-N-(3-Nitrophenyl)-2-Naphthalenecarboxamide

    • Product Name 3-Hydroxy-N-(3-Nitrophenyl)-2-Naphthalenecarboxamide
    • Alias HNNC
    • Einecs 632-011-3
    • 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

    894605

    Iupac Name 3-hydroxy-N-(3-nitrophenyl)naphthalene-2-carboxamide
    Molecular Formula C17H12N2O4
    Molecular Weight 308.29 g/mol
    Cas Number 1219964-48-3
    Appearance Solid
    Melting Point 218-222 °C
    Solubility Slightly soluble in DMSO, methanol
    Purity Typically >98%
    Storage Conditions Store at 2-8°C, protected from light and moisture

    As an accredited 3-Hydroxy-N-(3-Nitrophenyl)-2-Naphthalenecarboxamide factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle, 25 grams, sealed with tamper-evident cap, labeled with chemical name, CAS number, hazard pictograms, and handling instructions.
    Shipping The chemical **3-Hydroxy-N-(3-Nitrophenyl)-2-Naphthalenecarboxamide** is shipped in tightly sealed containers, protected from light and moisture. Shipments comply with local regulations for laboratory chemicals, typically via ground or air transport. Appropriate hazard labeling and documentation are included to ensure safe handling upon arrival. Temperature and handling requirements may apply.
    Storage Store **3-Hydroxy-N-(3-nitrophenyl)-2-naphthalenecarboxamide** in a tightly sealed container, in a cool, dry, and well-ventilated area, away from direct sunlight and moisture. Keep away from incompatible substances such as strong oxidizing agents and acids. Store at room temperature, and avoid exposure to heat and ignition sources. Follow appropriate chemical safety and handling guidelines.
    Application of 3-Hydroxy-N-(3-Nitrophenyl)-2-Naphthalenecarboxamide

    Applications of 3-Hydroxy-N-(3-Nitrophenyl)-2-Naphthalenecarboxamide in Industrial Manufacturing

    As a specialized manufacturer, we supply 3-Hydroxy-N-(3-Nitrophenyl)-2-Naphthalenecarboxamide to support advanced downstream processes across high-value industrial fields. Below are primary application sectors where this raw material demonstrates proven utility, with scenario-specific details on compliance, formulation, process, and end-product types.

    1. Organic Pigment Intermediates for High-Performance Coatings

    This chemical serves as an intermediate in the synthesis of complex naphthalene-based pigments, contributing to chromatic stability and dispersibility in industrial coatings. It supports the nucleophilic aromatic substitution step before final pigment precipitation, ensuring controlled shade and gloss in architectural and automotive applications. Quality standards for pigments used in coatings require rigorous trace impurity and heavy metal content management in the precursor stage.

    Industry compliance standards

    • ISO 4618: Paints and varnishes – Terms and definitions
    • EN 71-3:2019 (Migration of certain elements in coatings for toys and consumer products)
    • REACH Annex XVII (Restriction of hazardous substances in paint raw materials)
    • ASTM D3722 (Standard Test Method for Pigment Content in Paints and Coatings)

    Typical usage ratio

    • 5–12% w/w as a pigment intermediate relative to total batch weight, tailored based on required color strength and pigment architecture

    Downstream process integration

    • Introduced during diazotization or coupling step of pigment synthesis before final washing, milling, and dispersion into liquid or solid coatings matrices

    Final product types

    • PVC architectural coatings
    • OEM automotive paints
    • Industrial floor coatings
    • Powder coatings for appliances

    2. Dye Stuff Production for Technical Textile Applications

    In dye synthesis, 3-Hydroxy-N-(3-Nitrophenyl)-2-Naphthalenecarboxamide participates in condensation and ring-closure steps to generate disperse dyes, imparting strong color fastness and heat stability for synthetic fibers. Its consistent chemical profile supports precise color matching required in industrial polyester and acetate textile dyeing.

    Industry compliance standards

    • Oeko-Tex Standard 100 (Testing for harmful substances in dyed textiles)
    • ZDHC MRSL (Zero Discharge of Hazardous Chemicals Manufacturing Restricted Substances List)
    • ISO 105-C06 (Test for color fastness in textile dyeing)
    • REACH safety data guidelines for dye intermediates

    Typical usage ratio

    • 10–18% by molar ratio in final dye intermediate stage, adjusted by targeted chromophore intensity and batch-volume balancing

    Downstream process integration

    • Fed into the high-temperature reaction vessel during condensation or cyclization, preceded by controlled pH and temperature ramping, followed by quenching and filtration before dye standardization

    Final product types

    • Disperse dyes for polyester fabrics
    • Acetate fiber dyes
    • Technical textile inks
    • High-performance micro-dispersions for fiber blends

    3. Organic Electronics: Hole-Transport Material Synthesis

    Within the organic electronics sector, this material is used as a building block for functional hole-transport layers (HTLs), integrating into synthetic routes for OLED and OPV device manufacturing. Its molecular structure enables tunable electron affinity and stability under continuous current flow, supporting device longevity and efficiency metrics vital for consumer and industrial optoelectronics.

    Industry compliance standards

    • IEC 62341 (Organic Light Emitting Diode quality and safety requirements)
    • RoHS Directive (Restriction of hazardous substances for electronics manufacturing)
    • JEITA EIAJ ED-4701/200 (Reliability test methods for electronic materials)
    • ISO 9001:2015 (Quality Management Systems for electronics production)

    Typical usage ratio

    • 1–3 mol% in HTL precursor formulation, fine-tuned by target voltage threshold and layer thickness optimization in device prototypes

    Downstream process integration

    • Inserted during organic small-molecule synthesis (Suzuki or Buchwald-Hartwig coupling), then further purified before thin-film deposition by vacuum evaporation or spin-coating

    Final product types

    • OLED panel substrates for displays
    • Organic photovoltaic modules
    • Flexible lighting devices
    • Wearable display backplanes

    4. Pharmaceutical Synthesis: Intermediate for Antineoplastic Agents

    This compound functions as a precursor in multi-step synthesis pathways for producing naphthalenecarboxamide-based antineoplastic drugs. Control of residual nitro and hydroxy moieties is critical to comply with strict impurity limits and batch reproducibility demanded by regulated pharmaceutical manufacturing. All intermediate handling falls under cGMP and pharmacopoeial oversight.

    Industry compliance standards

    • ICH Q7: Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • US Pharmacopeia (USP General Chapters for intermediates)
    • European Pharmacopoeia Monograph 2037 (Intermediates for drug substance manufacturing)
    • 21 CFR Part 211 (US FDA cGMP requirements for finished pharmaceuticals)

    Typical usage ratio

    • Varies in the range of 0.8–2.5 equivalents per target molecule in key synthesis step, adjusted for reaction yield and purity targets

    Downstream process integration

    • Employed in palladium- or copper-catalyzed cross-coupling, followed by crystallization, then subjected to further derivatization before formation of the active pharmaceutical ingredient (API)

    Final product types

    • Naphthalene-derived antineoplastic drug substances
    • Small-molecule kinase inhibitors
    • Research-grade cytotoxic compound intermediates
    • API intermediate stock solutions for pharmaceutical synthesis

    5. Specialty Analytical Reagents

    Chemical and research laboratories use this molecule as a selectivity-modifying agent in advanced chromatography, and as a derivatization reagent in trace-level environmental and food analysis. Its structural properties enhance separation resolution and detection limits, especially for naphthalenic and nitroaromatic analytes in compliance-oriented analysis workflows.

    Industry compliance standards

    • ISO/IEC 17025 (General requirements for the competence of testing and calibration laboratories)
    • EPA SW-846 Methods (Analytical methods for hazardous waste)
    • USP General Chapter <621> (Chromatography)
    • AOAC Official Methods for Food Analysis

    Typical usage ratio

    • 0.1–0.5% w/v as derivatization agent, with adjustment based on analyte concentration and detection technique sensitivity

    Downstream process integration

    • Added prior to sample loading during chromatographic method setup, or during in-situ derivatization for HPLC and GC workflows

    Final product types

    • Certified reference solutions
    • Standardized analytical columns
    • Food contaminant test kits
    • Soil and water pollutant assay reagents
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