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N-(2-Chlorobenzyl)-N-Methylamine

    • Product Name N-(2-Chlorobenzyl)-N-Methylamine
    • Alias N-(Methyl)(2-chlorobenzyl)amine
    • Einecs 249-632-1
    • 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

    344140

    Chemical Name N-(2-Chlorobenzyl)-N-Methylamine
    Molecular Formula C8H10ClN
    Molecular Weight 155.62 g/mol
    Cas Number 73827-11-7
    Appearance Colorless to pale yellow liquid
    Boiling Point 238-240°C
    Density 1.08 g/cm3
    Solubility Soluble in organic solvents
    Smiles CN(CC1=CC=CC=C1Cl)C
    Inchi InChI=1S/C8H10ClN/c1-10-6-7-4-2-3-5-8(7)9/h2-5,10H,6H2,1H3
    Flash Point >110°C

    As an accredited N-(2-Chlorobenzyl)-N-Methylamine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle containing 100 grams of N-(2-Chlorobenzyl)-N-Methylamine, sealed with a screw cap and tamper-evident seal.
    Shipping N-(2-Chlorobenzyl)-N-methylamine should be shipped in sealed, chemical-resistant containers, clearly labeled according to applicable regulations. Store and transport it in a cool, dry, well-ventilated area away from heat and incompatible substances. Ship according to local, national, and international chemical safety standards, ensuring secure packaging to prevent leaks or spills during transit.
    Storage Store N-(2-Chlorobenzyl)-N-methylamine in a tightly sealed container, in a cool, dry, and well-ventilated area away from direct sunlight, heat sources, and incompatible materials such as strong oxidizers and acids. Avoid moisture exposure. Clearly label the container and keep it in a secure location, with appropriate safety signage and access limited to trained personnel. Use secondary containment when possible.
    Application of N-(2-Chlorobenzyl)-N-Methylamine

    Applications of N-(2-Chlorobenzyl)-N-Methylamine in Industrial Manufacturing

    N-(2-Chlorobenzyl)-N-Methylamine serves as an essential intermediate in various specialty chemical productions. Its performance and integration depend on strict process control, compliance with downstream sector regulations, and well-defined formulations. Below, we present key industrial applications based on real market demand and regulatory standards.

    1. Pharmaceutical Intermediate Synthesis

    This amine acts as a building block for synthesizing several active pharmaceutical ingredients (APIs), especially within the antihypertensive and antifungal drug classes. Manufacturers employ it in reaction steps requiring benzylamine moieties, following strict GMP protocols. Its use demands precise control to avoid residual intermediates in the final API, and any scale-up must adhere to validated cleaning and trace impurity limits.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • EU GMP Vol. 4 – Annex 1 & 2
    • United States Pharmacopeia (USP) general chapters
    • Chinese Pharmacopoeia (ChP) for APIs

    Typical usage ratio

    • Stoichiometric addition in molar equivalents relative to the target API intermediate (1.0-1.2 molar ratio per reaction step, adjusted based on desired purity and yield)

    Downstream process integration

    • Charged to the reactor during multi-step organic synthesis before key coupling or methylation reactions; purification through distillation or crystallization follows

    Final product types

    • Finished bulk APIs including antihypertensive agents
    • Pharmaceutical intermediates used in licensed drug production
    • Generic finished dosage forms (tablets, capsules) after further processing

    2. Agrochemical Synthesis

    Producers in the agrochemical sector utilize this compound to manufacture selective herbicide intermediates and some fungicidal active agents. Its chlorinated phenyl group enables unique reactivity for coupling steps, supporting scalable batch or continuous flow processes. Process engineers customize input levels to align with residue limits set by local and international authorities, safeguarding safety for downstream agricultural use.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • REACH registration requirements (EC No 1907/2006)
    • EPA Federal Insecticide, Fungicide, Rodenticide Act (FIFRA) for active ingredient traceability
    • ISO 9001:2015 for agricultural chemical production

    Typical usage ratio

    • Applied at 0.6–1.1 molar equivalents relative to target pesticide intermediate in batch syntheses; minor excess may be permitted for complete conversion in final steps

    Downstream process integration

    • Introduced during intermediate formation; commonly enters amidation, alkylation, or condensation stages followed by aqueous workup and solvent extraction

    Final product types

    • Selective herbicide intermediates
    • Fungicide pre-products
    • Formulated crop protection solutions in granular or liquid form after further compounding

    3. Fine Chemical Manufacturing for Specialty Dyes

    The specialty dyes industry incorporates this amine during syntheses of colorants requiring specific electron donor side chains, including advanced azo and anthraquinone derivatives. Manufacturers monitor reaction endpoints closely to limit unreacted amines in effluent, ensuring finished dye materials meet customer and environmental specifications. Process modifications accommodate differing dye structures and targeted performance attributes such as lightfastness and solubility.

    Industry compliance standards

    • OEKO-TEX Standard 100 (Annex 6) for textiles
    • ZDHC MRSL for restricted substances
    • ISO 9001:2015 for dye formulation and QC
    • EU REACH SVHC compliance for downstream importers

    Typical usage ratio

    • Ranges from 0.8–1.4 molar equivalents based on dye backbone and functionalization requirements

    Downstream process integration

    • Reacted in the main synthesis vessel during nucleophilic aromatic substitution or coupling; residue reduced through distillation and pH-adjusted wash steps

    Final product types

    • Specialty textile dyes
    • Colorants for inks and coatings
    • High-performance pigments for plastics and industrial applications

    4. Polymer Modifier Intermediate

    Polymer manufacturers use this compound as a modifier precursor in the production of specialty resins and engineering plastics. Its aromatic and amine functionalities impart specific thermal and electrical properties, supporting the fabrication of performance composites. Integration requires controlled handling to prevent side reactions and strict monitoring for final polymer composition. Adjustments to dosage influence resin mechanical strength, flexibility, and oxidation resistance.

    Industry compliance standards

    • ISO 9001:2015 for resin and polymer processes
    • UL 94 flammability standards for plastics
    • RoHS Directive 2011/65/EU for downstream electronic applications
    • GHS hazard classification for raw material handling

    Typical usage ratio

    • 0.5–2% by weight relative to base polymer resin; exact level set after small-scale compounding and mechanical property testing

    Downstream process integration

    • Blended into pre-polymerization feedstock; compounding occurs under inert atmosphere, followed by extrusion, curing, and molding to finished part

    Final product types

    • Modified thermoset resins
    • Engineering plastic parts
    • Specialty composite panels for automotive, electronics, or renewable energy sectors
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