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3-Chloro-4-Methylbenzylamine

    • Product Name 3-Chloro-4-Methylbenzylamine
    • Alias 3-Chloro-4-methylphenylmethanamine
    • Einecs 630-527-6
    • 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

    993850

    Productname 3-Chloro-4-Methylbenzylamine
    Casnumber 146137-75-3
    Molecularformula C8H10ClN
    Molecularweight 155.62
    Appearance Colorless to pale yellow liquid
    Boilingpoint 254-256 °C
    Density 1.12 g/cm3
    Purity Typically ≥98%
    Solubility Soluble in organic solvents (e.g., ethanol, DMSO)
    Smiles CC1=CC(=CC=C1Cl)CN
    Inchi InChI=1S/C8H10ClN/c1-6-2-3-7(9)5-8(6)4-10/h2-3,5H,4,10H2,1H3

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

    Packing & Storage
    Packing Amber glass bottle with secure screw cap, labeled "3-Chloro-4-Methylbenzylamine, 100g." Includes hazard symbols, batch number, and handling instructions.
    Shipping 3-Chloro-4-Methylbenzylamine is shipped in tightly sealed containers to prevent leakage and contamination. It should be transported according to applicable chemical regulations, away from incompatible materials, and in a cool, well-ventilated area. Proper labeling, documentation, and safety precautions such as protective handling and spill containment measures are strictly followed during shipping.
    Storage 3-Chloro-4-methylbenzylamine should be stored in a tightly sealed container in a cool, dry, well-ventilated area, away from sources of ignition, heat, and incompatible substances such as strong oxidizers. Protect from moisture and direct sunlight. Label clearly and ensure proper secondary containment. Store in accordance with local, state, and federal regulations for hazardous chemicals.
    Application of 3-Chloro-4-Methylbenzylamine

    Applications of 3-Chloro-4-Methylbenzylamine in Industrial Manufacturing

    As a direct manufacturer of 3-Chloro-4-Methylbenzylamine, we supply this fine chemical intermediate to global industrial partners across several high-value manufacturing sectors. Each application relies on specific quality grades, handling protocols, and regulatory adherence to maximize process compatibility and finished product safety. Below we present real-world industrial application scenarios organized by downstream sector, process integration, formulation practices, and dominant compliance regimes.

    1. Pharmaceutical Intermediate Synthesis

    Pharmaceutical manufacturers use this material primarily in the synthesis of specialty APIs, particularly in the preparation of substituted benzylamine scaffolds for antihypertensive and antiviral drug candidates. Batch synthesis protocols require precise metering of this amine for amidation and condensation reactions, directly impacting impurity profile and reaction yield. Our shipments comply with both industry pharmacopoeia monographs and customer-specific impurity profiles, enabling downstream users to meet regulatory expectations for intermediate control and traceability.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP/NF and Ph. Eur. monograph reference for related intermediates
    • EDQM Certification of Suitability (CEP) when processed into higher-value APIs
    • 21 CFR 211 (FDA) for traceability in API manufacturing environments

    Typical usage ratio

    • 0.3–1.5 molar equivalents relative to the acyl or carbonyl precursor, with adjustments based on step yield optimization and process scale

    Downstream process integration

    • Direct addition during the aminomethylation or reductive amination stage of multi-step API synthesis; introduced as a controlled addition under inert atmosphere; incorporation monitored via LC-MS in process analytical control (PAC)

    Final product types

    • Hydrochloride or free base pharmaceutical intermediates
    • Benzylamine-based API structures
    • Active ingredients for cardiovascular and antiviral formulations
    • Intermediate building blocks in specialty pharmaceutical fine chemicals

    2. Agrochemical Active Ingredient Development

    Crop protection product manufacturers employ this compound in the production of specific insecticide and herbicide intermediates. Its reactivity as an alkylating and nucleophilic agent supports the construction of active building blocks in both triazine and benzylamine-based agrochemicals. Handling and dosage levels correspond to strict occupational hygiene and effluent control requirements stipulated by regional agrochemical guidelines.

    Industry compliance standards

    • FAO/WHO Specification for Pesticide Active Ingredients (FAO/WHO)
    • ISO 9001:2015 for agrochemical ingredient traceability
    • REACH Regulation (EC) No 1907/2006 for import and downstream processing in the European Union
    • China GB/T 1601 standard for pesticide raw materials

    Typical usage ratio

    • 5–12% w/w as a functional amine reactant in the overall batch mass; varies based on the agrochemical active’s core structure and targeted synthesis pathway

    Downstream process integration

    • Introduced during the condensation or coupling stage with halogenated or electron-deficient substrates in stirred tank reactors; monitored by HPLC for endpoint detection and impurity profiling

    Final product types

    • Intermediates for selective herbicide actives
    • Benzylamine-derived insecticides
    • Fungicide precursor molecules
    • Seed treatment active ingredient intermediates

    3. Dye and Pigment Intermediate Manufacture

    3-Chloro-4-Methylbenzylamine acts as a specification-critical intermediate in the dye and pigment sector, notably for the production of azo and anthraquinone dyes. Producers incorporate it in the synthesis of colorant intermediates requiring electron-donating aromatic substituents. Strict raw material and product quality control ensures compliance with international textile and food contact colorant regulations.

    Industry compliance standards

    • OEKO-TEX® Standard 100 for textile dye components
    • EU Regulation (EC) No 1907/2006 REACH Annex XVII (restrictions on azo and aniline substances)
    • 21 CFR 74 (U.S. FDA) for certifiable food contact color additives
    • ISO 9001:2015 QMS for pigment and dye process verification

    Typical usage ratio

    • 2–7% by mass as an intermediate in the total pigment batch charge; fine-tuned for achieving target chromophore structure and color intensity

    Downstream process integration

    • Incorporated during diazotization or nucleophilic aromatic substitution reactions in closed-system batch reactors; addition rate controlled to synchronize with coupling partner reactivity and minimize byproduct formation

    Final product types

    • Textile dye chromogen intermediates
    • Food and pharmaceutical pigment precursors
    • Specialty ink colorants for printing and packaging
    • High-stability colorant additives for plastics and coatings manufacturing

    4. Polymer Additive and Functional Monomer Synthesis

    This compound serves a key function in the synthesis of specialized functional monomers and in the modification of polymer backbones for performance materials. Major downstream users design application-specific oligomers and crosslinkers by leveraging the reactivity of the aromatic amine. End-use specifications require tight control of monomer purity and trace impurity content, as low-level contaminants can affect polymerization kinetics and finished polymer performance.

    Industry compliance standards

    • ISO 9001:2015 for additive and monomer manufacturing
    • Global Automotive OEM requirements on non-volatile residue for polymer additives
    • ASTM D6288 standard practice for purity verification of specialty polymer intermediates
    • EU Regulation (EC) No 10/2011 on food contact polymers (where applicable)

    Typical usage ratio

    • 0.5–5% by mass relative to total monomer blend in copolymerizations; adjusted according to the required functional group incorporation and desired polymer molecular weight

    Downstream process integration

    • Added into polymerization or pre-polymer step as a chain-stopping or branching agent; typically charged before initiator addition; process parameters set based on calorimetry and inline viscosity monitoring

    Final product types

    • Performance polymeric additives for adhesives and coatings
    • Functionalized oligomers for reactive hot-melt adhesives
    • Engineered thermoset resins with tailored flexibility and strength
    • Monomeric precursors for specialty plastics and composite matrix materials
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