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4-Nitroanthranilic Acid

    • Product Name 4-Nitroanthranilic Acid
    • Alias 4-nitro-2-aminobenzoic acid
    • Einecs 217-665-5
    • 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

    544588

    Chemical Name 4-Nitroanthranilic Acid
    Molecular Formula C7H6N2O4
    Molecular Weight 182.14 g/mol
    Appearance Yellow to orange crystalline powder
    Melting Point 212-215°C
    Solubility In Water Slightly soluble
    Cas Number 619-17-0
    Pubchem Cid 12206
    Density 1.59 g/cm³
    Iupac Name 2-amino-4-nitrobenzoic acid
    Smiles C1=CC(=C(C=C1C(=O)O)N)[N+](=O)[O-]

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

    Packing & Storage
    Packing Amber glass bottle, 100g, with screw cap; white hazard label showing "4-Nitroanthranilic Acid," CAS number, and safety pictograms.
    Shipping 4-Nitroanthranilic Acid is shipped in tightly sealed containers, protected from light, moisture, and incompatible substances. It is classified as hazardous, requiring appropriate labeling and documentation. Transport follows local and international regulations for chemicals. Personal protective equipment is recommended during handling to avoid inhalation, ingestion, or skin contact during shipping and receiving.
    Storage 4-Nitroanthranilic acid should be stored in a cool, dry, and well-ventilated area away from direct sunlight and sources of ignition. Keep the container tightly closed and clearly labeled. Store separately from incompatible substances such as strong oxidizers and reducing agents. Use chemical-resistant containers and ensure appropriate spill containment measures are in place to prevent environmental contamination.
    Application of 4-Nitroanthranilic Acid

    Applications of 4-Nitroanthranilic Acid in Industrial Manufacturing

    4-Nitroanthranilic acid remains an essential intermediate for multiple chemical synthesis pathways across several downstream industries. As a direct manufacturer, we work closely with formulation scientists, process engineers, and QC specialists from global downstream partners to ensure precise integration of our material into high-specification industrial workflows. Below, we detail key application scenarios where this raw material provides functional value according to current regulatory, technical, and production requirements.

    1. Dyes and Pigments Production

    Leading dyestuff manufacturers incorporate 4-nitroanthranilic acid as a core building block in the synthesis of azo and anthraquinone-based dyes. This application relies on the compound’s ability to introduce nitro and amino functionalities, delivering color performance and stability in textile dyeing formulations. Integration takes place primarily in the diazotization and coupling stages, directly influencing shade purity and lightfastness properties.

    Industry compliance standards

    • REACH Regulation (EC) No 1907/2006 for chemical substances
    • OEKO-TEX® Standard 100 Annex 4 (textile raw materials, dyes, and auxiliaries)
    • ZDHC MRSL v3.1 (Zero Discharge of Hazardous Chemicals)
    • China GB/T 21866-2008 for industrial dyes

    Typical usage ratio

    • Formulators dose at 2.0–6.5% by weight in azo dye coupling bases; exact percentage depends on desired chromophore structure and batch yield calculations.

    Downstream process integration

    • Introduced during initial synthesis for diazotization with nitrosyl sulfuric acid, followed by coupling with aromatic amines or phenols to yield target dye intermediates.

    Final product types

    • Reactive dyes, disperse dyes, acid dyes, direct dyes for textile and leather industries

    2. Pharmaceutical Intermediates

    Pharmaceutical API facilities employ 4-nitroanthranilic acid as a key starting compound for manufacturing certain anti-tuberculosis agents and anti-inflammatory drugs. Its chemical backbone supports transformation into substituted quinolines and related heterocyclic actives, with stringent control over impurity profiles and trace-level by-products essential during cGMP production.

    Industry compliance standards

    • ICH Q7: Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP–NF (United States Pharmacopeia–National Formulary) for raw material quality
    • EU GMP Part II for intermediates
    • China Pharmacopoeia (ChP) 2020 Edition

    Typical usage ratio

    • Used at 1.8–4.2 molar equivalents, adjusted based on specific route of synthesis for quinoline or anthranilamide derivatives as dictated by synthesis protocol scale.

    Downstream process integration

    • Integrated during the early condensation and cyclization phases; undergoes reduction, chlorination, or coupling steps ahead of final API crystallization.

    Final product types

    • Pharmaceutical intermediates for sulfamethoxazole, substituted quinolines, and anti-tuberculosis drugs

    3. Agricultural Chemical Synthesis

    Major agrochemical companies employ this compound as a synthetic intermediate in the production of selective herbicides and fungicidal active ingredients. Formulators exploit its functional groups to build nitrogen-containing ring systems, which become the core of systemic crop protection agents. The process demands careful control to achieve regulatory-specified purity and minimize residual contaminants.

    Industry compliance standards

    • FAO/WHO Specification for Plant Protection Products (JMPS)
    • ISO 9001:2015 Quality Management for agrochemical manufacturing
    • China ICAMA (Institute for the Control of Agrochemicals, Ministry of Agriculture) registration standards
    • EU Regulation (EC) No 1107/2009 for plant protection products

    Typical usage ratio

    • Typically 0.8–3.0 molar parts per synthetic batch, with ratio determined by target molecule conversion efficiency and downstream purification capacity.

    Downstream process integration

    • Enters the process during ring closure and nitration reactions, often followed by halogenation or alkylation before formulation as technical concentrate.

    Final product types

    • Herbicide intermediates, technical grade fungicides, pre-mix pesticide ingredients

    4. Fluorescent Whitening Agents (FWAs) Manufacturing

    Producers of optical brighteners utilize 4-nitroanthranilic acid as a precursor for synthesizing advanced stilbene and biphenyl-based FWAs. Its molecular structure enables the formation of conjugated systems required for blue-emitting compounds, with tight control of reaction sequence to ensure purity and UV-resistance for final plastic or detergent applications.

    Industry compliance standards

    • EN 71-3:2019 (Migration of certain elements in toys and plastics)
    • ISO 9001/ISO 14001 Certification for specialty chemical production
    • REACH SVHC (Substances of Very High Concern) compliance
    • China GB 9685-2016 (National standard for food contact additives, plastics)

    Typical usage ratio

    • Usage level ranges from 1.5–5.0% by weight in the synthesis step for FWA intermediates, refined according to targeted absorption spectra and polymer compounding requirements.

    Downstream process integration

    • Applied in the condensation step with diphenylamine or stilbene derivatives, forming the key intermediate for final sulfonation or amination stages.

    Final product types

    • Optical brighteners for synthetic fibers, laundry detergents, high-grade plastics, and paper coatings
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