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2,4-Dichloro-3,5-Dinitrobenzoic Acid

    • Product Name 2,4-Dichloro-3,5-Dinitrobenzoic Acid
    • Alias Dinoan
    • Einecs 221-001-9
    • 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

    365818

    Productname 2,4-Dichloro-3,5-Dinitrobenzoic Acid
    Casnumber 1509-85-5
    Molecularformula C7H2Cl2N2O6
    Molecularweight 298.01 g/mol
    Appearance Yellow crystalline powder
    Meltingpoint 235-237°C
    Solubility Slightly soluble in water; soluble in organic solvents like acetone and ethanol
    Boilingpoint Decomposes on heating
    Density 1.82 g/cm³ (approximate)
    Purity Typically ≥98%
    Smiles C1=C(C(=C(C(=C1Cl)[N+](=O)[O-])C(=O)O)[N+](=O)[O-])Cl
    Storagetemperature Store at 2-8°C
    Synonyms 2,4-Dichloro-3,5-dinitrobenzoic acid

    As an accredited 2,4-Dichloro-3,5-Dinitrobenzoic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 100g bottle of 2,4-Dichloro-3,5-Dinitrobenzoic Acid comes in a tightly sealed amber glass container with hazard labels.
    Shipping 2,4-Dichloro-3,5-Dinitrobenzoic Acid is shipped in tightly sealed containers, protected from light and moisture. It is classified as a hazardous material due to its potential toxicity and requires compliant labeling and documentation. Transport should follow applicable regulations for dangerous goods, ensuring safe handling and storage conditions throughout transit.
    Storage 2,4-Dichloro-3,5-Dinitrobenzoic Acid should be stored in a cool, dry, well-ventilated area, away from incompatible substances such as bases and strong oxidizers. Keep the container tightly closed and protect from light and moisture. Store in a corrosion-resistant container, clearly labeled, and avoid exposure to heat or open flame. Ensure proper chemical waste and spill management procedures are in place.
    Application of 2,4-Dichloro-3,5-Dinitrobenzoic Acid

    Applications of 2,4-Dichloro-3,5-Dinitrobenzoic Acid in Industrial Manufacturing

    As a specialized producer of 2,4-Dichloro-3,5-Dinitrobenzoic Acid, we supply this compound to established sectors where strict formulation, quality assurance, and regulatory frameworks define its integration. Our material supports chemical synthesis processes with a focus on industry-proven contexts where its specific reactivity and chemical profile underpin downstream transformations. Below, we outline primary industrial applications, each detailed with authentic practice information to support your formulation and manufacturing planning.

    1. Intermediate for Veterinary Drug Synthesis

    Manufacturers in the veterinary pharmaceuticals sector use this compound as a nitration and chlorination source in the synthesis of benzoic acid derivatives. Its high purity ensures consistent functionalization during the preparation of APIs for animal health medications, where QC-tested input materials are essential for batch reproducibility and downstream compliance.

    Industry compliance standards

    • EU GMP for Veterinary Medicinal Products (Directive 2001/82/EC and 2019/6/EU)
    • VICH GL9 (Good Manufacturing Practice Guidance for Active Pharmaceutical Ingredients)
    • US FDA 21 CFR Part 211 (Current Good Manufacturing Practice for Finished Pharmaceuticals)
    • Ph. Eur. Monographs (as applicable for finished products)

    Typical usage ratio

    • Reaction charge range: 0.5–2.5 mol equivalents, directly related to target molecule yield and downstream recovery step efficiency

    Downstream process integration

    • Reacts during API precursor step as an electrophilic benzene ring partner or functional group donor before multi-step purification and crystallization

    Final product types

    • Veterinary antiparasitic tablets and injectables
    • Animal feed additives with benzoic acid core structures
    • Blended premix veterinary medicinal products

    2. Key Intermediate for Herbicide Active Ingredient Production

    Producers of selective herbicides employ this compound as a core building block in the formation of advanced benzoic acid-type actives. The dinitro and dichloro substitution pattern provides the chemical backbone required in manufacturing certain post-emergence weed control agents used in commercial agriculture, where reaction yield and low byproduct profile are critical for economic viability.

    Industry compliance standards

    • FAO/WHO Specifications (JMPS) for Pesticides
    • EPA 40 CFR Part 158 (Data Requirements for Pesticides)
    • REACH Regulation (EC) No 1907/2006
    • ISO 9001:2015 Quality Management for Agrochemicals

    Typical usage ratio

    • Used at 0.8–1.2 molar equivalents for most condensation reactions, adjusted to maintain active ingredient formation in multi-tonne batch processes

    Downstream process integration

    • Stagewise input at initial or secondary coupling during the synthesis of benzoic acid-derived herbicidal cores, before formulation and granulation

    Final product types

    • Selective post-emergent herbicide granules and concentrates
    • Water-dispersible agrochemical powders
    • Chemical intermediates for crop-protection active substance registration dossiers

    3. Intermediate for Specialty Pigment Synthesis

    Advanced pigment manufacturers utilize this compound in the tailored synthesis of high-performance azo and nitro pigments. Its well-defined substitution pattern allows for controlled coupling and diazotization reactions, enabling colorant producers to create shades with precise chromatic and fastness characteristics for plastics, inks, and coating industries based on end-customer requirements.

    Industry compliance standards

    • EN 71-3:2019 (Safety of Toys — Migration of Certain Elements)
    • ISO 1248:2006 (Pigments – Methods of test for basic properties)
    • ASTM D476 (Standard Classification for Dry Pigmentary Titanium Dioxide Products)
    • REACH Annex XVII (Restriction of hazardous substances in pigments)

    Typical usage ratio

    • Intermediate introduced at 0.6–1.4 equivalents per batch, optimally tuned for shade strength and dispersibility in pigment mass production

    Downstream process integration

    • Added at first or second functionalization point in multi-step pigment development before purification, finishing, and micronization

    Final product types

    • High-stability organic pigment powders for plastics applications
    • Advanced dispersible pigment formulations for solvent-based inks
    • Color-fast coating pastes for industrial finishes

    4. Synthesis Intermediate for Electronic Grade Chemicals

    Producers of specialty materials for microelectronic device manufacturing employ this raw material in processes demanding ultra-high purity. It enables introduction of dinitrobenzoic acid moieties into chemical precursors for liquid crystal components and specialty resins, where consistent reactivity, minimal residual metals, and tight batch-to-batch control are enforced to match downstream semiconductor reliability requirements.

    Industry compliance standards

    • JEITA ET-5003 (Standard for Electronic Grade Chemical Materials)
    • SEMI C1-0815 (Specifications for Liquid Chemicals Used in Semiconductor Processing)
    • IATF 16949:2016 (Quality Management for Automotive Sector Electronics)
    • IEC 62474 (Material Declaration for Products of and for the Electrotechnical Industry)

    Typical usage ratio

    • Standard addition level set at 0.3–0.9 molar equivalents, aligned with downstream purity targets and absence of critical trace contaminants

    Downstream process integration

    • Integrated at the functionalization stage of precursor resins or LC intermediates, prior to final purification and electronic grade certification

    Final product types

    • Specialty resins for photoresist fabrication
    • LC device intermediate chemicals
    • Precursors for microelectronic adhesive materials
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