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Methyl 4-Chloro-3-Nitrobenzoate

    • Product Name Methyl 4-Chloro-3-Nitrobenzoate
    • Alias Methyl 4-chloro-3-nitrobenzoate
    • Einecs EINECS 251-882-5
    • 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
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    Specifications

    HS Code

    965924

    Product Name Methyl 4-Chloro-3-Nitrobenzoate
    Cas Number 14389-43-0
    Molecular Formula C8H6ClNO4
    Molecular Weight 215.59 g/mol
    Appearance Yellow crystalline solid
    Melting Point 64-67°C
    Solubility Slightly soluble in water; soluble in organic solvents
    Density 1.54 g/cm³ (approximate)
    Purity Typically ≥ 98%
    Smiles COC(=O)C1=CC(=C(C=C1)Cl)[N+](=O)[O-]
    Inchi InChI=1S/C8H6ClNO4/c1-14-8(11)5-2-3-6(9)7(4-5)10(12)13/h2-4H,1H3
    Storage Conditions Store in a cool, dry place, tightly closed

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

    Packing & Storage
    Packing A 100g amber glass bottle with secure screw cap, labeled "Methyl 4-Chloro-3-Nitrobenzoate," hazard symbols, and batch details.
    Shipping **Shipping Description:** Methyl 4-Chloro-3-Nitrobenzoate should be shipped in tightly sealed containers, protected from light and moisture. Handle with care as it may be harmful if inhaled, ingested, or upon skin contact. Transport according to regulations for hazardous chemicals, with appropriate labeling and documentation. Store in a cool, dry, well-ventilated area.
    Storage Methyl 4-Chloro-3-Nitrobenzoate should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from heat, sparks, and sources of ignition. Protect from direct sunlight and moisture. Keep separate from incompatible materials such as strong oxidizing agents and reducing agents. Label the container clearly and handle with appropriate personal protective equipment (PPE).
    Application of Methyl 4-Chloro-3-Nitrobenzoate

    Applications of Methyl 4-Chloro-3-Nitrobenzoate in Industrial Manufacturing

    Methyl 4-Chloro-3-Nitrobenzoate finds critical use as a key intermediate in specialized sectors of industrial chemical synthesis, including advanced pharmaceutical APIs, crop protection formulations, dyes, and specialty polymer additives. By integrating this compound into diverse downstream operations, manufacturers achieve precise customization in high-value product lines under strict regulatory guidance.

    1. Pharmaceutical Active Pharmaceutical Ingredient (API) Synthesis

    Our clients in the pharmaceutical sector rely on this material for the targeted synthesis of several advanced APIs, including non-steroidal anti-inflammatory drugs (NSAIDs) and select antihypertensive agents. As a precursor in multi-step organic syntheses, it is essential for introducing specific electron-withdrawing and halogen-substituted aromatic groups, which are key for final molecule activity. We ensure strict lot traceability and purity thresholds according to customer route requirements, facilitating reproducibility in reaction yields and impurity profiles.

    Industry compliance standards

    • Current Good Manufacturing Practice (cGMP, ICH Q7)
    • USP–NF, EP, and JP monographs for designated finished APIs
    • FDA and EMA guidelines for starting material qualification
    • REACH and GHS chemical safety documentation

    Typical usage ratio

    • 5–15% molar equivalent as an intermediate per batch, adjusted based on specific synthetic route and scale
    • Ratio varies according to yield optimization and target impurity thresholds

    Downstream process integration

    • First chlorination/nitration step feeding into ester saponification and subsequently to amidation stages
    • Isolates introduced via controlled charge points in batch or semi-continuous reactors
    • Careful temperature and pH monitoring during stepwise coupling reactions

    Final product types

    • API intermediates for NSAIDs (e.g., diclofenac, indomethacin derivatives)
    • Building blocks for antihypertensive agents
    • Regulatory-submitted bulk pharmaceutical chemicals

    2. Agrochemical Intermediate Manufacturing

    This compound serves as a core precursor in the synthesis of several modern selective herbicides and fungicides. With its reactive chloro and nitro functional groups, it enables halogenated benzoic acid derivative formation, critical in developing actives for broadleaf weed control and crop disease resistance. End users benefit from consistent impurity profiles and the capability to scale synthesis to multi-ton production, meeting regulatory residue and specification limits.

    Industry compliance standards

    • FAO/WHO Joint Meeting on Pesticide Specifications (JMPS)
    • ISO 9001 for product traceability in crop protection manufacturing
    • REACH registration and transport classification
    • EU Regulation 1107/2009 for plant protection products

    Typical usage ratio

    • 10–18% by weight of the active ingredient batch, tuned to the nature of the targeted pesticide structure
    • Adjustments based on the conversion rate in subsequent functional group refinements

    Downstream process integration

    • Direct feed into cyanation, hydrolysis, or reduction reactions for tailoring to final molecule structure
    • Charged at early esterification stages, ensuring full conversion by post-reaction hydrolysis
    • Blending under inert nitrogen for stability during multi-stage synthesis lines

    Final product types

    • Benzoic acid-derived herbicide actives (e.g., chlorinated benzoic acid analogs)
    • Precursor for triazole and imidazole fungicide classes
    • Select insecticide intermediates

    3. Dye and Pigment Intermediate

    Colorants producers utilize this compound as a selective coupling intermediate in azo, anthraquinone, and nitro dye synthesis. The chloro and nitro functionalities enable strong chromophoric system development, allowing manufacturers to control wavelength absorption, mordant compatibility, and wash fastness properties in textile dyeing and specialty pigment blends. Tight batch reproducibility is maintained to ensure color consistency for high-spec end-use demands.

    Industry compliance standards

    • Oeko-Tex® Standard 100 for restricted substances in dyes
    • EN 71-3 for safety of toy colorants
    • ISO 9001 process and quality controls
    • REACH Annex XVII restricted Azo colorants list

    Typical usage ratio

    • 8–22% relative to the mass of the coupling component blend, dependent on the target chroma intensity
    • Optimized for batch yield versus color strength requirements in textile and pigment applications

    Downstream process integration

    • Added to diazotization or nucleophilic aromatic substitution sequences
    • Feeds parallel syntheses for pre-mix pigment dispersion steps
    • Employed in closed reactor systems to control release of volatile by-products

    Final product types

    • Disperse and reactive dyes for synthetic and cellulosic fibers
    • Specialty pigments for plastics, inks, and coatings
    • Chromophore building-blocks for advanced colorant chemistries

    4. Specialty Polymer Additive Synthesis

    Specialty polymer manufacturers use this compound to create functionalized monomers or cross-linkers. Its electron-deficient aromatic ring is valuable in building halogenated, nitro-substituted polymer blocks, especially for flame retardant and chemical-resistant applications. Its integration contributes to key performance properties in engineering plastics and adhesives, where precise functionalization levels are required for regulatory and performance certification.

    Industry compliance standards

    • UL 94 Flame Retardancy Certification
    • RoHS (Restriction of Hazardous Substances Directive) compliance
    • ISO 14001 environmental management for polymer additives
    • REACH Substances of Very High Concern (SVHC) lists

    Typical usage ratio

    • 3–10% polymer additive weight, dependent on target property modification and base resin chemistry
    • Levels adjusted during R&D according to mechanical, fire, and solvent resistance specifications

    Downstream process integration

    • Fed into pre-polymerization step or as chain-terminating/cross-linking agent in batch processes
    • Direct addition to compounding lines under temperature-controlled conditions
    • Required moisture and impurity controls at additive blending stage

    Final product types

    • Halogenated engineering thermoplastics
    • Flame-retardant polymer masterbatches
    • Adhesives and sealants with enhanced chemical resistance
    Free Quote

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