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4-Methyl-3-Nitrobenzoic Acid

    • Product Name 4-Methyl-3-Nitrobenzoic Acid
    • Alias 4-Methyl-3-nitrobenzoic acid
    • Einecs 226-749-0
    • 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

    800565

    Product Name 4-Methyl-3-Nitrobenzoic Acid
    Cas Number 619-17-0
    Molecular Formula C8H7NO4
    Molecular Weight 181.15
    Appearance Yellow crystalline powder
    Melting Point 193-195 °C
    Solubility In Water Slightly soluble
    Density 1.47 g/cm³
    Pka 2.7
    Purity Typically ≥98%
    Storage Conditions Store at room temperature, keep tightly closed
    Smiles CC1=CC(=CC(=C1)C(=O)O)[N+](=O)[O-]
    Inchi InChI=1S/C8H7NO4/c1-5-2-3-6(8(10)11)7(4-5)9(12)13/h2-4H,1H3,(H,10,11)

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

    Packing & Storage
    Packing 100g amber glass bottle with tamper-evident cap, labeled "4-Methyl-3-Nitrobenzoic Acid," including hazard symbols and handling instructions.
    Shipping **Shipping Description:** 4-Methyl-3-Nitrobenzoic Acid should be shipped in tightly sealed containers, protected from light and moisture. It must be packed according to chemical safety regulations, clearly labeled, and accompanied by SDS documentation. Ship via a licensed chemical carrier, adhering to all local, state, and international regulations for hazardous materials.
    Storage 4-Methyl-3-nitrobenzoic acid should be stored in a cool, dry, and well-ventilated area, away from sources of heat and incompatible substances such as strong oxidizing agents. Keep the container tightly closed and protected from moisture and direct sunlight. Properly label the storage area and ensure access is restricted to trained personnel, following all relevant safety regulations.
    Application of 4-Methyl-3-Nitrobenzoic Acid

    Applications of 4-Methyl-3-Nitrobenzoic Acid in Industrial Manufacturing

    4-Methyl-3-Nitrobenzoic Acid serves as a key intermediate in several industrial manufacturing segments, with its use centered on specialty chemical synthesis and downstream value-added formulation. As a direct manufacturer, we support formulation specialists and process engineers in the adoption of 4-Methyl-3-Nitrobenzoic Acid for high-value applications where proven process compatibility and documented industry compliance standards are critical to product quality and regulatory acceptance. Below, we outline authentic downstream application scenarios based on current global manufacturing practices and customer formulations.

    1. Intermediate for API (Active Pharmaceutical Ingredient) Synthesis

    Producers of certain non-steroidal anti-inflammatory drugs (NSAIDs) and related APIs employ 4-Methyl-3-Nitrobenzoic Acid as an early-stage building block in multi-step pharmaceutical synthesis. The compound enters the process as a precursor in the nitration and methylation paths, enabling efficient ring transformation prior to amide coupling or reduction steps. Its use is subject to stringent purity criteria, and formulation chemists adjust input quantities according to targeted yield and downstream impurity profiling requirements driven by regional registration files.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice Guidance for APIs
    • European Pharmacopeia (Ph. Eur.) monographs as applicable to downstream APIs
    • US FDA cGMP for Active Pharmaceutical Ingredients (21 CFR Part 210/211)
    • Chinese Pharmacopoeia for regulated pharmaceutical intermediates

    Typical usage ratio

    • 0.85–1.2 molar equivalents per reaction batch, depending on targeted conversion and side product management; stoichiometry adjusted during route scouting and scale-up

    Downstream process integration

    • Introduced during the early synthesis steps as a primary aromatic acid intermediate, typically dissolved or suspended in aprotic solvents, followed by sequential reduction or amidation depending on the synthetic route

    Final product types

    • Non-steroidal anti-inflammatory drug APIs (e.g., specific methylated benzoic derivatives licensed in certain markets)
    • Pharmaceutical intermediates for analgesic and antipyretic medications

    2. Colorant and Pigment Precursor Manufacturing

    The compound finds use among specialty pigment manufacturers as a nitrated aromatic precursor for azo and anthraquinone dye synthesis. In this sector, process engineers use it to introduce specific electron-withdrawing groups, maximizing dye fastness and color intensity in the finished colorant molecules. The selection of reactant ratios and timing of dosing aligns with proprietary pigment design targets and end-use performance criteria for industrial coatings and plastics.

    Industry compliance standards

    • REACH Regulation (EC) No 1907/2006 for industrial chemicals
    • EN 71-3:2019 Safety of Toys - Migration of certain elements (relevant for pigments in toys)
    • ISO 8124—Safety standards for children's products, relevant for pigmented end uses
    • Color Index (CI) registration, as applicable to downstream pigments

    Typical usage ratio

    • 5–20% by weight of total pigment intermediate charge, tuned according to desired chromophore strength and purity specifications in subsequent coupling reactions

    Downstream process integration

    • Dosed into diazotization and coupling reactors under controlled pH and temperature, facilitating the formation of colorant backbones used in high performance organic pigments

    Final product types

    • Azo pigments for printing inks and coatings
    • Anthraquinone dyes for plastics and fiber coloring
    • Specialty organic pigments for automotive finishes

    3. Synthesis of Agrochemical Intermediates

    In the crop protection sector, manufacturers employ this compound as a fundamental structural unit during the assembly of selective herbicide and fungicide active ingredients. Agrochemical chemists integrate it within multi-step processes where aromatic functionalization is essential for biological activity tuning, often leveraging its ortho-substituted nitro and methyl groups for specific product classes. Usage rates depend on downstream molecule complexity and overall batch size within the production facility.

    Industry compliance standards

    • FAO/WHO Joint Meeting on Pesticide Specifications (JMPS) requirements for technical material
    • Globally Harmonized System of Classification and Labeling of Chemicals (GHS)
    • ISO 9001 Quality Management for agrochemical synthesis
    • China GB 4839-2004 and EU Plant Protection Product (PPP) registration standards

    Typical usage ratio

    • 3–10% of total reactant mass, varying with chosen synthetic pathway and target technical concentration for active ingredient isolation

    Downstream process integration

    • Reacted during key nitration or reduction steps in batch or continuous synthesis processes; material introduced after charge of base substrate for subsequent chlorination or amination according to product formulation

    Final product types

    • Herbicide intermediates for selective weed control formulations
    • Fungicide precursors designed for systemic crop disease management

    4. Advanced Materials and Polymer Additive Synthesis

    Producers of engineering plastics and specialty elastomers introduce the compound into polymer additive synthesis routes, using it as a targeted modifier or chain extender for advanced polymer properties. It provides defined aromatic substitution patterns, supporting downstream application for electronics, automotive, and high-performance consumer goods, where strict non-interference with mechanical or dielectric properties is essential. Industrial formulation teams select dosage parameters based on the required functional group density in final polymers.

    Industry compliance standards

    • RoHS Directive (2011/65/EU) for restricted substances in electronics
    • UL 94 flammability classification for plastic materials
    • ISO 9001 and ISO 14001 for quality and environmental management in advanced materials production
    • Food Contact Compliance (EU 10/2011) if intended for indirect food applications

    Typical usage ratio

    • 0.5–3% by weight in additive masterbatch, set according to specified end-use property enhancement and compatibility with copolymer components

    Downstream process integration

    • Added directly during the pre-polymerization or compounding stage, typically using solvent-assisted blending or melt extrusion systems to ensure uniform distribution in the functionalized polymer matrix

    Final product types

    • High-performance polymers for automotive and consumer electronics
    • Polymer additive masterbatches for electrical and gasketing applications
    • Customized engineering plastics with enhanced durability or chemical resistance
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