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Ethyl 3-Nitrobenzoate

    • Product Name Ethyl 3-Nitrobenzoate
    • Alias m-Nitobenzoic acid ethyl ester
    • Einecs 210-589-7
    • 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

    832664

    Product Name Ethyl 3-Nitrobenzoate
    Chemical Formula C9H9NO4
    Molecular Weight 195.17 g/mol
    Cas Number 99-63-8
    Appearance Yellow crystalline solid
    Melting Point 61-63°C
    Boiling Point 315°C
    Solubility In Water Slightly soluble
    Density 1.32 g/cm³
    Refractive Index 1.570
    Purity Typically ≥98%
    Storage Temperature Store at room temperature

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

    Packing & Storage
    Packing The 100g Ethyl 3-Nitrobenzoate comes in a tightly sealed amber glass bottle with a printed chemical label and safety warnings.
    Shipping Ethyl 3-Nitrobenzoate is shipped in tightly sealed containers, protected from light, moisture, and incompatible materials. It is typically packed according to transport regulations for organic chemicals, labeled as a non-hazardous substance unless otherwise specified. Proper labeling and documentation accompany all shipments to ensure safe and compliant handling during transit.
    Storage Ethyl 3-nitrobenzoate should be stored in a cool, dry, well-ventilated area away from sources of heat, sparks, or open flames. Keep the container tightly closed and protected from light, moisture, and incompatible substances such as strong acids, bases, and oxidizing agents. Store in a tightly sealed chemical-resistant container, following all relevant chemical safety regulations and labeling requirements.
    Application of Ethyl 3-Nitrobenzoate

    Applications of Ethyl 3-Nitrobenzoate in Industrial Manufacturing

    Ethyl 3-Nitrobenzoate serves as a critical intermediate in various chemical manufacturing processes. As an experienced manufacturer, we address diverse downstream integrations across specialty chemicals, pharmaceuticals, agrochemicals, dyes, and advanced materials, with a focus on real application workflows and recognized compliance requirements.

    1. Pharmaceutical Intermediate Synthesis

    Pharmaceutical companies utilize Ethyl 3-Nitrobenzoate mainly in the synthesis of active pharmaceutical ingredients, especially in the preparation of substituted benzoic acids and related moieties for anti-inflammatory and antimicrobial agents. It enters the process during nitroaromatic compound synthesis, often through ester hydrolysis or amidation, to generate key intermediates like 3-aminobenzoic acid derivatives. Downstream applications rely on precise stoichiometric control to ensure the purity and yield required by regulated drug production environments.

    Industry compliance standards

    • ICH Q7 GMP for Active Pharmaceutical Ingredients
    • European Pharmacopoeia (Ph. Eur.) monographs for intermediates
    • 21 CFR Part 211 (US FDA) for pharmaceutical manufacturing
    • Chinese Pharmacopoeia (ChP), depending on final API registration

    Typical usage ratio

    • 0.8 to 1.2 molar equivalents per target benzoic acid intermediate, adjusted for downstream conversion efficiency

    Downstream process integration

    • Charged to reactor for direct ester hydrolysis or amidation
    • Pre-purification step prior to reduction for amine synthesis
    • Used in catalytic hydrogenation or nitration steps for further transformation
    • Subjected to acid/base work-up for high-purity intermediate isolation

    Final product types

    • 3-Aminobenzoic acid derivatives
    • Non-steroidal anti-inflammatory drug (NSAID) precursors
    • Pharmaceutical grade benzoic acid analogues
    • Specialty chemical intermediates for drug manufacturing

    2. Agrochemical Synthesis

    Manufacturers involved in crop protection solutions integrate Ethyl 3-Nitrobenzoate during the creation of nitroaromatic and aminobenzoic scaffolds, foundational for various herbicidal and fungicidal agents. It participates in selective ester hydrolysis, amide coupling, or chlorination steps, impacting the downstream specificity and activity profile of the end products. Formulators adjust input amounts based on the target yield and crop protection active registration requirements, as defined by regulatory dossiers.

    Industry compliance standards

    • OECD Guidelines for Testing of Chemicals (relevant to synthesis safety and efficacy)
    • FAO/WHO specifications for technical material
    • EU Regulation (EC) No 1107/2009 for plant protection products
    • Chinese GB/T 1603 standards for pesticide intermediates

    Typical usage ratio

    • 5–25% w/w of the synthetic matrix, or 0.8–1.5 molar equivalents per precursor batch, optimized by downstream hydrolysis or reduction efficiency

    Downstream process integration

    • Direct batch input for base-catalyzed hydrolysis
    • Precursor reagent for amide bond formation with agrochemical backbones
    • Feeds into reduction steps for amine-based pesticide synthesis
    • Post-reaction work-up with solvent extraction and drying

    Final product types

    • Aminobenzoate-based herbicides
    • Nitroaromatic fungicide intermediates
    • Pre-emergent weed control actives
    • Agrochemical technical grade input chemicals

    3. Dye and Pigment Intermediate Production

    Producers of specialty dyes and colorants employ Ethyl 3-Nitrobenzoate for the synthesis of nitroaromatic chromophores and azo dye precursors. The compound undergoes reduction, diazotization, and condensation with phenols or aromatic amines, enabling the creation of shades with tailored lightfastness and solubility properties. Manufacturers operate within strict purity tolerances to prevent downstream contamination of dye lots, and the ratio depends on color depth and target molecular structure.

    Industry compliance standards

    • REACH Registration, Evaluation, Authorisation and Restriction of Chemicals (EU)
    • OEKO-TEX Standard 100 for colorant inputs where required
    • ISO 9001:2015 quality management systems in dye manufacturing
    • Global Harmonized System (GHS) for safe handling and hazard communication

    Typical usage ratio

    • 10–40% of main charge for chromophore synthesis, variable by final dye strength and reactive site requirements

    Downstream process integration

    • Introduced to batch during nitro-reduction steps
    • Involved in diazotization and subsequent coupling for azo dyes
    • Added pre-crystallization for high-purity pigment isolation
    • Subject to multi-stage filtration and drying ahead of blending and coloration

    Final product types

    • Nitrobenzene-based azo dyes
    • Modified anthraquinone pigments
    • Disperse dyes for textile application
    • Organic pigments for plastics and inks

    4. Advanced Materials and Specialty Polymer Additives

    Polymers and specialty material producers incorporate Ethyl 3-Nitrobenzoate as a functional intermediate in the synthesis of aromatic polyesters, photoresists, and advanced polymeric additives. The compound performs as a controlled nitration agent and monomer modifier, contributing to properties such as UV stability or specific reactivity in final materials. The input levels and reaction sequence depend strictly on the desired polymer chain structure and target additive loadings required for product certification.

    Industry compliance standards

    • ISO 14001 environmental management for polymer plants
    • RoHS Directive 2011/65/EU for electronics additives
    • ASTM D638–14 for polymer tensile properties (where relevant)
    • REACH SVHC (Substances of Very High Concern) screening for additives

    Typical usage ratio

    • 2–8% by mass of overall monomer input, dependent on target molecular weight and functional performance

    Downstream process integration

    • Early stage feed for polycondensation or copolymerization reactions
    • Intermediate stage modifier in photoresist resin compounding
    • Input for in situ functionalization during advanced material processing
    • Blending and compounding for targeted end-use certification

    Final product types

    • Aromatic polyesters for engineering applications
    • UV-stable specialty polymers
    • Photoresist resins for semiconductor processes
    • Custom polymer additives for electronics and coatings
    Free Quote

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