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3-Chloro-N-Methylaniline

    • Product Name 3-Chloro-N-Methylaniline
    • Alias m-Chloro-N-methylaniline
    • Einecs 202-334-0
    • 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

    598248

    Cas Number 14386-56-8
    Molecular Formula C7H8ClN
    Molecular Weight 141.6 g/mol
    Iupac Name 3-chloro-N-methylaniline
    Appearance Colorless to pale yellow liquid
    Boiling Point 232-234 °C
    Density 1.17 g/cm³
    Flash Point 107 °C
    Solubility In Water Slightly soluble
    Refractive Index 1.583
    Smiles CNc1cccc(Cl)c1

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

    Packing & Storage
    Packing 3-Chloro-N-Methylaniline, 100g, packaged in a tightly sealed amber glass bottle with hazard labeling and chemical information clearly displayed.
    Shipping 3-Chloro-N-Methylaniline is shipped in tightly sealed containers, protected from moisture and direct sunlight. It should be stored in a cool, well-ventilated area away from incompatible substances. Ensure proper labeling and compliance with local and international transport regulations for hazardous chemicals. Handle with care due to its toxic and potentially flammable nature.
    Storage 3-Chloro-N-Methylaniline should be stored in a tightly closed container, in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible materials such as strong oxidizers. Keep away from direct sunlight and moisture. Ensure proper labeling and store at room temperature or as recommended by the supplier. Use appropriate secondary containment to prevent spills or leaks.
    Application of 3-Chloro-N-Methylaniline

    Applications of 3-Chloro-N-Methylaniline in Industrial Manufacturing

    As the original manufacturer of 3-Chloro-N-Methylaniline, we have observed its consistent use in several high-value industrial sectors. The material functions as a key intermediate in the synthesis of advanced chemicals for pharmaceuticals, agrochemicals, dye manufacturing, and pigment industries. In all application scenarios, precise handling and adherence to industry-specific standards remain vital for product safety, regulatory acceptance, and end product performance across global markets.

    1. Pharmaceutical Intermediate Synthesis

    Large-scale pharmaceutical companies use this compound to manufacture active pharmaceutical ingredients (APIs), particularly for antihypertensive and antitumor agents. It acts as a starting molecule in multi-step synthesis through specific regioselective transformations, such as acylation or coupling reactions, under GMP-compliant conditions, where purity and traceability directly affect final drug safety profiles.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP & EP Monographs for process intermediates
    • 21 CFR Part 211 (FDA Current Good Manufacturing Practice)
    • EDQM TSE Certification for API supply chain

    Typical usage ratio

    • Mole-to-mole equivalence to subsequent ring-activated or substituted anilines, typically 1.1:1 to 1.3:1 vs target end molecule, depending on synthesis route yield optimization

    Downstream process integration

    • Primary introduction occurs during the condensation stage with carboxylic or sulfonic acid derivatives, followed by purification and protection/deprotection steps before final ring closure or alkylation stages

    Final product types

    • Sartans (e.g., Valsartan intermediates)
    • Imidazoline antihypertensives
    • Oncological small molecule precursors
    • Benzimidazole API intermediates

    2. Agrochemical Active Ingredient Production

    Technical-grade 3-Chloro-N-Methylaniline forms the essential aromatic core for synthesis of several selective herbicides, fungicides, and insecticides. Major global crop protection producers formulate using precise batch reactions in line with regional agricultural regulations, maintaining strict impurity profiles to meet residue safety requirements at scale.

    Industry compliance standards

    • FAO/WHO Joint Meeting on Pesticide Specifications (JMPS)
    • ISO 9001:2015 for agrochemical manufacturing
    • REACH Annex II for hazardous intermediates management
    • EPA 40 CFR Part 158 Subpart G for inert ingredient residuals

    Typical usage ratio

    • Applied at 0.8 to 1.4 mole per batch production run versus final active ingredient, varying by molecular route and percentage yield in multi-step synthesis

    Downstream process integration

    • Introduced after initial halogenation or methylation of benzene rings, followed by cyclization or amide formation, before formulation and granulation for field-ready products

    Final product types

    • Acylaniline herbicides (e.g., pretilachlor, butachlor intermediates)
    • Triazole fungicides precursors
    • Aromatic insecticide intermediate compounds

    3. Specialty Dye Intermediate Manufacture

    3-Chloro-N-Methylaniline has a long-established role in the colorant sector, particularly for synthesizing azo and anthraquinone dyes used in textiles and inks. Its selective electron-donating properties enable controlled coupling and diazotization, resulting in high-purity intermediates for subsequent chromophore formation. Leading dye houses require consistent product traceability and batch-to-batch uniformity in line with applicable EU and US regulations for textile and paper dyes.

    Industry compliance standards

    • OEKO-TEX Standard 100 (Textile Dye Safety)
    • EU REACH Annex XVII restrictions for aromatic amines
    • ISO 9001:2015 certified quality systems
    • ZDHC MRSL (Zero Discharge of Hazardous Chemicals Manufacturing Restricted Substance List)

    Typical usage ratio

    • Incorporated at 0.3 to 0.9 mole per mole of coupling component, depending on desired color intensity and batch process yield

    Downstream process integration

    • Added post-nitration stage and prior to diazotization and coupling with phenolic counterparts, generally in solvent-based or aqueous batch reactors

    Final product types

    • Azo dye intermediates for synthetic fiber processing
    • Anthraquinone dye precursors for polyester applications
    • Inkjet ink colorant intermediates

    4. Pigment and Colorant Additive Synthesis

    Major pigment manufacturers incorporate this intermediate to produce vibrant, stable colorants used in plastics, elastomers, and coatings. The compound participates in condensation and oxidative coupling reactions, particularly for the development of highly transparent and high lightfastness pigments intended for automotive and packaging markets. Strict regulatory control is necessary to ensure migration and residue limits are not exceeded in end use applications.

    Industry compliance standards

    • EN 71-3 Safety of Toys - Migration of certain elements (for pigment use in toys)
    • EU Regulation (EC) No 1907/2006 (REACH) for chemical safety
    • ASTM D476 (Standard Classification for Dry Pigmentary Titanium Dioxide Products)
    • ISO 14001 for environmental management in pigment production

    Typical usage ratio

    • Utilized at 0.5 to 1.2 equivalents relative to main pigment-forming aromatic substrate, carefully adjusted for target color shade and application substrate compatibility

    Downstream process integration

    • Fed into condensation and homocoupling synthesis reactors, then further processed through filtration, milling, and surface modification for pigment stabilization

    Final product types

    • Organic pigment concentrates for polymer coloration
    • High-performance coatings colorants
    • Elastomer color masterbatches

    5. Synthesis of Corrosion Inhibitor Intermediates

    Chemical processing plants and oilfield service companies use this material to manufacture aromatic corrosion inhibitor intermediates, which help extend equipment life and improve operational reliability in challenging environments. By reacting under controlled amination or amidation protocols, the compound delivers specific molecular features needed for adsorption efficiency and hydrophobicity in end formulations. Strict compliance with occupational and process safety standards is maintained throughout.

    Industry compliance standards

    • API RP 752/753 for chemical processing safety
    • OSHA 29 CFR 1910 (Process Safety Management)
    • IEEE Std 841 for corrosion resistance in rotating equipment environments
    • ISO 45001 for occupational health and safety management in chemical plants

    Typical usage ratio

    • Formulated at 1.0 to 1.5 molar equivalents versus amine or heterocyclic core component, with adjustments based on required adsorption isotherm targets in specific oilfield and industrial cooling water applications

    Downstream process integration

    • First introduced during the ring-amination or ring-amidation steps in corrosion inhibitor intermediate synthesis, followed by reaction pathway steps tailored for target substrate selectivity

    Final product types

    • Aromatic corrosion inhibitor intermediates for oil and gas pipelines
    • Protective additives for industrial cleaning fluids
    • Chemical agents for closed-loop water treatment systems
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