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3,4-Dichloro-N-Methylaniline

    • Product Name 3,4-Dichloro-N-Methylaniline
    • Alias N-Methyl-3,4-dichloroaniline
    • Einecs 611-230-3
    • 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

    623821

    Cas Number 612-62-4
    Molecular Formula C7H7Cl2N
    Molecular Weight 176.05 g/mol
    Appearance Colorless to pale yellow liquid
    Boiling Point 269-271°C
    Density 1.305 g/cm3
    Purity Typically ≥98%
    Solubility Insoluble in water; soluble in organic solvents
    Synonyms N-Methyl-3,4-dichloroaniline
    Flash Point 122°C
    Refractive Index 1.580 (approx.)

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

    Packing & Storage
    Packing 250g of 3,4-Dichloro-N-Methylaniline is packaged in a sealed amber glass bottle with a hazard label and screw cap.
    Shipping **Shipping Description (approx. 50 words):** 3,4-Dichloro-N-Methylaniline should be shipped in tightly sealed, chemical-resistant containers, protected from light and moisture. Transport must comply with local, national, and international hazardous material regulations. It should be clearly labeled and accompanied by appropriate safety documentation (SDS). Handle with care, using secondary containment to prevent leaks or spills during transit.
    Storage 3,4-Dichloro-N-Methylaniline should be stored in a tightly closed container in a cool, dry, and well-ventilated area, away from moisture, heat sources, and incompatible substances such as oxidizing agents and strong acids. Keep it out of direct sunlight and store under inert atmosphere if possible. Ensure the storage area is equipped with appropriate spill containment and labeled according to chemical safety regulations.
    Application of 3,4-Dichloro-N-Methylaniline

    Applications of 3,4-Dichloro-N-Methylaniline in Industrial Manufacturing

    3,4-Dichloro-N-Methylaniline plays a critical role as a building block in a range of high-value chemical synthesis routes. Below, we provide a detailed overview of its established industrial applications across several downstream sectors, including information about regulatory requirements, typical formulation ratios, integration into manufacturing workflows, and types of finished goods produced by direct customers.

    1. Agrochemical Synthesis: Herbicide Intermediate

    Leading crop protection chemical manufacturers employ this compound as a strategic intermediate in the synthesis of selective herbicides, particularly those in the aniline and phenoxyacetic acid family. Its chemical structure enables formation of active molecules that target broadleaf weeds in cereal and oilseed cultivation. The substance is introduced during the condensation and chlorination stages, requiring careful control under regulated production protocols to ensure safe handling and product traceability through each batch. Each formulation run is configured in accordance with the downstream target molecule specifications, as dictated by crop geography and resistance management programs.

    Industry compliance standards

    • FAO/WHO Specifications for Agricultural Pesticides
    • OECD Test Guidelines for Chemical Safety
    • REACH Registration (EC 1907/2006) for intermediate status
    • ISO 9001:2015 Quality Management System

    Typical usage ratio

    • Ranges from 0.8 to 1.5 molar equivalents per batch, adjusted according to the purity of the input and the desired active ingredient yield

    Downstream process integration

    • Direct charge into the condensation reactor during stepwise amination or chlorination leading to the target herbicidal compound

    Final product types

    • Selectively active herbicides for commercial agricultural formulations
    • Technical-grade active ingredients for further downstream formulation

    2. Pharmaceutical API Intermediate for Antihypertensive Agents

    Innovator and generic pharmaceutical producers use this molecule as a core intermediate in multi-step syntheses of certain antihypertensive drug substances. High purity and consistent lot-to-lot quality are crucial in this segment, given ICH and cGMP guidelines governing all intermediates leading to APIs for human health. The compound’s addition must meet in-process control targets through accurate weighing before chlorination or reductive amination, maintaining strict traceability throughout the closed production cycle until finished API crystallization.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • 21 CFR Part 211 cGMP for Finished Pharmaceuticals
    • USP–NF and EP monograph requirements for API intermediates (where applicable)
    • FDA DMF (Drug Master File) referencing for regulatory submission

    Typical usage ratio

    • Utilized at a stoichiometric ratio, typically 1.0 to 1.2 equivalents relative to the target pharmaceutical intermediate, set according to in-process residual analysis and final assay requirements

    Downstream process integration

    • Dosed into the main synthetic route at the step of intermediate coupling, preceding the cyclization or side-chain introduction steps in antihypertensive molecule development

    Final product types

    • Bulk pharmaceutical intermediates for API plants
    • Registered antihypertensive drug substances exported to global regulated markets

    3. Dye and Pigment Manufacturing

    This aniline derivative serves as a key raw material for the synthesis of specialty dyes and colorants, including vat and azo dye classes, widely utilized in textile, leather, and plastics sectors. Compliance with international dye standards is essential due to downstream environmental regulations, especially REACH Annex XVII and established OEKO-TEX requirements governing banned amine content. In practice, the material is introduced as a reactant during the diazotization and coupling steps, where its substitution pattern delivers desirable chromatic properties to final pigments and finished dye blends.

    Industry compliance standards

    • REACH (EC Regulation 1907/2006) restriction on aromatic amines
    • OEKO-TEX Standard 100 for textile dyes
    • ISO 9001 certification for dye plant operations
    • ZDHC Wastewater Guidelines for effluent compliance

    Typical usage ratio

    • Added at 1.0 to 2.0 molar equivalents per formula, adjusted based on target dye shade and chromophore strength needed per mass of finished product

    Downstream process integration

    • Introduced at the diazotization and subsequent coupling stage to form key color-bearing intermediates or end-use pigments

    Final product types

    • Vat, azo, and anthraquinone dyes for textile coloration
    • High-purity organic pigments for plastics compounding and printing inks

    4. Specialty Chemicals: Industrial Corrosion Inhibitor Intermediate

    Manufacturers in the specialty chemicals sector incorporate this raw material in the synthesis of tailored arylamine derivatives used as industrial corrosion inhibitors, especially for use in water treatment and oilfield operations. Strict adherence to chemical substance registration protocols, occupational exposure limits, and environmental control goals shapes every batch. Typical dosing rates depend on the structure-activity relationship studies run by R&D for targeted anti-corrosion performance, often fed into multi-step N-alkylation or further chlorination lines. End formulations are intended for direct use in heavy industry applications where consistent performance is essential.

    Industry compliance standards

    • OECD Guidelines for Testing of Chemicals
    • U.S. EPA TSCA (Toxic Substances Control Act) chemical inventory listing
    • EU CLP Regulation (EC 1272/2008) for classification and labeling
    • ISO 14001 Environmental Management Standard

    Typical usage ratio

    • Ranges from 0.5 to 1.2 moles per mole of base inhibitor backbone, fine-tuned according to laboratory screening outcomes on corrosion resistance

    Downstream process integration

    • Fed into the alkylation or further functionalization reactor, forming the active corrosion inhibitor moiety prior to blending and packaging

    Final product types

    • Corrosion inhibitor concentrates for water treatment plants
    • Additive packages for oilfield pipelines and refinery operations
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