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2-Methylaniline

    • Product Name 2-Methylaniline
    • Alias o-Toluidine
    • Einecs 202-429-0
    • 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

    945746

    CAS_Number 95-53-4
    IUPAC_Name 2-Methylaniline
    Molecular_Formula C7H9N
    Molecular_Weight 107.15 g/mol
    Appearance Colorless to pale yellow liquid
    Melting_Point -2 °C
    Boiling_Point 200 °C
    Density 1.00 g/cm³
    Solubility_in_Water Slightly soluble
    Flash_Point 87 °C
    Odor Aromatic amine-like
    Vapor_Pressure 0.33 mmHg at 25 °C

    As an accredited 2-Methylaniline 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 500 mL of 2-Methylaniline, with hazard labels, secure screw cap, and tamper-evident seal.
    Shipping 2-Methylaniline (o-Toluidine) should be shipped in tightly sealed containers, properly labeled, and stored in a cool, dry, well-ventilated area. It is classified as a hazardous material (UN 1708) and must be transported according to relevant regulations, with protective measures to avoid exposure, leaks, or incompatible substances.
    Storage 2-Methylaniline should be stored in a tightly closed, clearly labeled container in a cool, dry, well-ventilated area away from sources of ignition, heat, and incompatible substances like oxidizers and acids. Protect from light and moisture. Use secondary containment to prevent leaks or spills, and ensure access to safety equipment such as eyewash stations and spill kits.
    Application of 2-Methylaniline

    Applications of 2-Methylaniline in Industrial Manufacturing

    As a specialized producer of high-purity 2-Methylaniline (o-toluidine), we supply this aromatic amine to key industries where consistent quality and process compatibility are essential for advanced downstream manufacturing. Below we detail the primary fields in which 2-Methylaniline enables valued transformations, with a focus on practical compliance, formulation, industrial integration, and end-use products specific to each sector.

    1. Synthesis of Azo Dyes for Textile and Leather Processing

    Textile and leather manufacturers use 2-Methylaniline as a direct coupling component for producing azo dyes with tailored hues, fastness properties, and application suitability across cotton, wool, and natural leather tanning. Demand for stable and vibrant coloration drives precision in batch formulation to ensure both product safety and regulatory adherence, along with reproducibility in processing lines handling elevated volumes or continuous flows. Manufacturers select 2-Methylaniline to produce specific dye intermediates such as o-toluidine-based azo compounds, supporting both mass coloration and specialized pattern applications.

    Industry compliance standards

    • REACH Regulation (EC) No 1907/2006—authorization and restriction of aromatic amines in dye manufacture
    • OEKO-TEX® Standard 100—harmonized test for prohibited amine residues in finished textiles
    • ZDHC Manufacturing Restricted Substances List (MRSL)—restrictions on aniline derivatives used in dye synthesis
    • ISO 105 series—color fastness and safety testing methods for final textiles and leathers

    Typical usage ratio

    • Intermediate or coupling component: 3–12% by weight in dye synthesis; adjustment depends on targeted dye structure and chromophore intensity

    Downstream process integration

    • Nitration and reduction precursor, then direct diazotization or condensate formation in dye batch reactors; dosing precision critical in color tuning and residue minimization

    Final product types

    • Reactive and direct azo dyes for cotton, viscose, and wool fibers
    • Fastness-improved acid dyes for natural and synthetic leather
    • Printing inks and coloring pastes for fashion and technical textile coatings

    2. Manufacture of Rubber Antioxidants and Vulcanization Accelerators

    Rubber compounding industries incorporate 2-Methylaniline as a raw material for antioxidant and accelerator molecules critical to the vulcanization process for both general-purpose and specialty rubber applications. Mechanically intensive uses such as tire tread, conveyor belts, and molded automotive parts require rubber matrices with long-term resistance to heat, oxidation, and chemical degradation. The amine structure lends itself to the synthesis of key intermediates such as IPPD and 6PPD, used for their performance in delaying aging and cracking during product service life.

    Industry compliance standards

    • ISO 9001—quality management systems for rubber chemical formulation
    • ASTM D4671—testing protocols for antidegradants and antioxidants in rubber
    • China GB/T 2570—standards for vulcanization accelerators and antioxidants
    • EU End-of-Life Vehicle (ELV) Directive—restriction of hazardous substances in automotive rubber parts

    Typical usage ratio

    • Feedstock for antioxidants: 5–18% calculation basis in intermediate chemical synthesis; actual use depends on target molecular yield and purity
    • Indirect presence in final rubber compound: 0.2–3 phr (parts per hundred rubber) via the antioxidant or accelerator additive

    Downstream process integration

    • Amine introduction during fine chemical synthesis of antioxidant and accelerator intermediates, followed by granulation, blending, and formulation into rubber masterbatches via Banbury mixing or open-mill compounding

    Final product types

    • High-performance rubber tires for passenger cars and commercial vehicles
    • Industrial hoses, belts, and vibration-damping products
    • Automotive molded parts requiring enhanced ozone and oxidative stability
    • Elastomeric adhesives and sealants

    3. Production of Agricultural Crop Protection Agents

    Agrochemical synthesis uses 2-Methylaniline as a building block in the manufacture of certain herbicides and insecticides, supporting both broad-acre and specialty crop applications. The core aromatic amine structure enables creation of active ingredients and intermediates that require precise reactivity for effectiveness and controlled environmental impact. Downstream formulators apply rigorous QC to minimize residual amine in the final active substances, as mandated by regulatory bodies, and integrate 2-Methylaniline at critical stages of multi-step synthesis routes for modern crop protection products.

    Industry compliance standards

    • FAO/WHO Specifications for Pesticides—guidance on allowable impurity profiles and formulation practices
    • EU Regulation (EC) No 1107/2009—approval of active substances for plant protection
    • US EPA FIFRA—Federal Insecticide, Fungicide, and Rodenticide Act requirements for registration, purity, and labeling
    • ISO 17025—accredited analytical testing of amine impurities in actives

    Typical usage ratio

    • Key precursor: 8–25% by weight of the total active ingredient synthesis, varying with molecular design and batch scale

    Downstream process integration

    • Initial alkylation or acylation for building heterocyclic pesticide cores; process involves controlled addition and subsequent purification to achieve target isomer distribution and yield

    Final product types

    • Herbicides for selective broadleaf weed control (e.g., toluidine-derived active molecules)
    • Insecticide technical concentrates and formulated emulsifiable concentrates
    • Pre-emergence and post-emergence crop protection solutions for cereals and specialty plantation crops

    4. Intermediate for Pharmaceutical Synthesis

    The pharmaceutical industry utilizes 2-Methylaniline as a synthesis intermediate for select active pharmaceutical ingredients (APIs), particularly where aromatic amines enable necessary functionalization of molecular scaffolds. Downstream processes involving 2-Methylaniline require strict segregation, traceability, and monitoring to meet purity and impurity specifications set by global pharmacopoeias and local health authorities. Trace amounts can participate in multi-step syntheses, advancing core structures that yield therapeutic agents after subsequent functional transformations and stringent purification.

    Industry compliance standards

    • ICH Q7—Good Manufacturing Practice Guide for Active Pharmaceutical Ingredients
    • USP-NF, EP, and JP—regional pharmacopoeia monographs and residual solvent frameworks
    • CFR Title 21 Part 211—current Good Manufacturing Practice for finished pharmaceuticals (FDA)
    • EudraLex Volume 4—EU GMP guidelines for primary manufacturing and traceability

    Typical usage ratio

    • Intermediate or impurity precursor: 2–10% of process batch, with adjustments based on yield and final step purification losses

    Downstream process integration

    • Sulfonation, condensation, or ring modification reactions in API raw synthesis; controlled addition in reactor vessels with inline QC for batch traceability

    Final product types

    • Antihyperlipidemic API intermediates
    • Sulfonamide pharmaceutical agents
    • Pain relief API structures where methylamino aromatic building blocks are required

    5. Synthesis of Epoxy and Polyurethane Hardener Intermediates

    Two-component adhesive and coating manufacturers require select hardeners based on aromatic amine chemistry to control curing kinetics, crosslink density, and mechanical performance. 2-Methylaniline functions as a key reactant in synthesizing substituted aromatic diamines, which become integral to curing systems for specialized epoxy and polyurethane applications. Stringent management of purity ensures predictable hardening behavior, physical stability, and compliance with occupational and environmental health standards.

    Industry compliance standards

    • ISO 9001—quality management in specialty chemical processes
    • REACH Annex XVII—substance-specific restrictions for consumer and industrial coatings
    • Directive 2010/75/EU—VOC and emission limits for industrial coatings
    • EN 1504-2—performance requirements for protective coatings on concrete structures

    Typical usage ratio

    • Amine precursor: 6–22% by weight in hardener synthesis; varies by desired reactivity and degree of cross-linking

    Downstream process integration

    • Incorporation into hardener molecule synthesis, followed by blending into formulated curing agents; further addition during 2K epoxy or PU resin mixing prior to application

    Final product types

    • High-strength chemical-resistant epoxy flooring systems
    • Protective metal coatings and tank linings
    • Polyurethane adhesives for industrial assembly
    • Composite resin matrices for building and automotive structures
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