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4-Chloro-3-Nitrophenylacetic Acid

    • Product Name 4-Chloro-3-Nitrophenylacetic Acid
    • Alias 4-Chloro-3-nitrobenzeneacetic acid
    • Einecs 257-464-9
    • 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

    227400

    Product Name 4-Chloro-3-Nitrophenylacetic Acid
    Cas Number 4126-29-6
    Molecular Formula C8H6ClNO4
    Molecular Weight 215.59 g/mol
    Appearance Yellow solid
    Melting Point 153-156°C
    Solubility Slightly soluble in water
    Purity Typically ≥98%
    Storage Conditions Store at room temperature, tightly closed
    Synonyms 2-(4-Chloro-3-nitrophenyl)acetic acid
    Smiles C1=CC(=C(C=C1Cl)N(=O)=O)CC(=O)O

    As an accredited 4-Chloro-3-Nitrophenylacetic 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 labeled "4-Chloro-3-Nitrophenylacetic Acid, 25g," with hazard symbols, chemical formula, and lot/batch information displayed.
    Shipping 4-Chloro-3-Nitrophenylacetic Acid is shipped in tightly sealed containers to protect from moisture and light. It should be labeled as a hazardous chemical, with handling precautions indicated. Shipment follows regulations for organic solids, stored at room temperature, away from incompatible substances, and includes proper documentation for safe and secure transit.
    Storage **4-Chloro-3-Nitrophenylacetic Acid** should be stored in a tightly sealed container, in a cool, dry, well-ventilated area away from incompatible substances such as strong oxidizers and bases. Protect from light and moisture. Label the container clearly and avoid prolonged exposure to air and heat to maintain chemical stability. Follow all relevant safety and regulatory guidelines during storage.
    Application of 4-Chloro-3-Nitrophenylacetic Acid

    Applications of 4-Chloro-3-Nitrophenylacetic Acid in Industrial Manufacturing

    4-Chloro-3-nitrophenylacetic acid supports several high-value downstream industries as a precision intermediate, particularly where strict quality measures and well-established industrial standards shape material selection. Our manufacturing processes focus on delivering consistent specification and traceability to facilitate safe, compliant, and reliable use in recognized applications. Below are the primary industry segments that directly utilize this compound in large-scale manufacturing, each with scenario-specific regulatory context, technical integration details, and typical product outcomes.

    1. Pharmaceutical Intermediate for Cephalosporin Synthesis

    This material serves as a key acylating agent in the production of various third-generation cephalosporin antibiotics. Many pharmaceutical API facilities rely on its structure for the synthesis of side chains in cephalosporin active pharmaceutical ingredients through multi-step reactions involving nucleophilic substitution. Process engineers prioritize high purity and low isomeric impurities at this stage to comply with stringent regulatory filings for final API export certification.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • European Pharmacopoeia (EP) monographs for cephalosporins
    • US Pharmacopeia (USP) General Chapters relevant to beta-lactam APIs
    • China GMP (2010 Revision) for antibiotic intermediates

    Typical usage ratio

    • 1.05–1.15 molar equivalent relative to the core beta-lactam in side-chain acylation. Process R&D may adjust upward to compensate for losses in purification or down to minimize post-reaction cleavage byproducts.

    Downstream process integration

    • Material is introduced during protected side-chain formation prior to deprotection and crystallization steps; acylation runs in polar aprotic solvents under temperature-controlled conditions.

    Final product types

    • Sterile injectable cephalosporin APIs (such as cefdinir, cefixime, cefpodoxime)
    • Oral cephalosporin finished dosages
    • Bulk antibiotic intermediates supplied to formulation plants

    2. Agrochemical Intermediate for Phenoxyacetic Acid Herbicides

    Industrial crop protection producers employ this compound to build selective herbicide molecules, where it acts as a precursor in Grignard and condensation reactions forming 4-chloro-3-nitrophenoxyacetic acid derivatives. The ability to tightly control the halogen and nitro group placement determines its value for regulatory approval and downstream performance in field formulations.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • REACH registration under Regulation (EC) No 1907/2006
    • ISO 9001:2015 certified quality management for raw material batches
    • Chinese Ministry of Agriculture GB 20810 for pesticide intermediates

    Typical usage ratio

    • 0.85–1.20 weight equivalent per mole of final acetic acid derivative. In pilot scale, adjustment occurs based on stoichiometric yield and impurity formation controls during phenoxyacetic condensation steps.

    Downstream process integration

    • Added into the condensation reactor following magnesium reagent introduction; undergoes neutralization and extraction before further transformation into the active ingredient.

    Final product types

    • Selective phenoxy herbicides for wheat, rice, and maize
    • Emulsifiable concentrate (EC) and suspension concentrate (SC) pesticide formulations
    • Intermediate bulk solutions shipped for downstream esterification

    3. Dye Intermediate in the Synthesis of Specialty Azo Dyes

    Specialty dye manufacturers leverage this compound to introduce nitro and chloro groups into aromatic dye structures, enhancing hue stability and affinity for synthetic textile fibers. Its precise functionalization allows for reproducible diazotization and coupling, a critical stage in the production of heat-resistant, highly pure azo dyes for industrial textiles.

    Industry compliance standards

    • OEKO-TEX Standard 100, Appendix 6 (restricted aromatic amines and nitro-compounds)
    • ISO 9001:2015 for dye intermediate production
    • ZDHC MRSL (Zero Discharge of Hazardous Chemicals) conformance in textile supply
    • GB/T 22864 Chemical Fiber Dyeing Industry Standard

    Typical usage ratio

    • 0.90–1.05 mole equivalent relative to the azo coupling agent in dye synthesis. Exact ratio determined by chromophore yield and lightfastness requirements specified in batch QC procedures.

    Downstream process integration

    • Reacted in the diazotization stage, followed by coupling and isolation of dye intermediates before purification for final dye manufacturing.

    Final product types

    • Reactive and disperse dyes for polyester and nylon
    • High-temperature fast dyes for automotive and industrial fabrics
    • Custom colorants used in synthetic fiber extrusion

    4. Fine Chemical Intermediate in Electronic Materials Synthesis

    Producers of specialty electronic chemicals use this compound as a precursor for constructing high-purity aromatic building blocks employed in substrates and advanced polymeric materials. The electron-withdrawing groups facilitate selective substitution in multi-step syntheses, supporting the electrical and thermal properties needed in next-generation circuit board resins and advanced display films.

    Industry compliance standards

    • IPC-4101B specification for base materials for printed circuit boards
    • ISO 14001:2015 environmental management for specialty chemicals
    • RoHS Directive 2011/65/EU (Restriction of Hazardous Substances)
    • UL 94 standard for flammability of plastic components

    Typical usage ratio

    • 0.88–1.10 mole equivalent depending on downstream polymer chain length and functional requirements of the end resin formulation, as defined by internal process validation.

    Downstream process integration

    • Incorporated in nucleophilic aromatic substitution or esterification during the early functionalization phase. The purified intermediate then continues to polycondensation steps for resin formation.

    Final product types

    • Resins for high-frequency printed circuit boards
    • Optically clear films for LCD and OLED panels
    • Custom-formulated insulating materials for microelectronics
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