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N-Methyl-2-(Trifluoromethoxy)Aniline

    • Product Name N-Methyl-2-(Trifluoromethoxy)Aniline
    • Alias N-Methyl-o-(trifluoromethoxy)aniline
    • Einecs 'Einecs': 693-373-5
    • 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
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    Specifications

    HS Code

    591852

    Product Name N-Methyl-2-(Trifluoromethoxy)Aniline
    Cas Number 886763-02-0
    Molecular Formula C8H8F3NO
    Molecular Weight 191.15
    Appearance Colorless to pale yellow liquid
    Boiling Point 208-210°C
    Density 1.29 g/cm3
    Purity Typically ≥ 98%
    Solubility Soluble in organic solvents
    Smiles CNc1ccccc1OC(F)(F)F
    Synonyms 2-(Trifluoromethoxy)-N-methylaniline
    Refractive Index 1.500-1.510
    Flash Point 89°C
    Storage Conditions Store at 2-8°C, keep container tightly closed

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

    Packing & Storage
    Packing 25g of N-Methyl-2-(Trifluoromethoxy)Aniline is packaged in a sealed amber glass bottle with a tamper-evident cap and safety label.
    Shipping N-Methyl-2-(Trifluoromethoxy)Aniline should be shipped in tightly sealed containers, protected from light, moisture, and incompatible materials. Transport must comply with local and international chemical regulations, using appropriate labeling and documentation. Ship via courier services authorized for chemical transport, ensuring secondary containment to prevent leaks or spills during transit.
    Storage Store N-Methyl-2-(Trifluoromethoxy)aniline in a tightly sealed container, away from moisture, heat, and direct sunlight. Keep in a cool, dry, and well-ventilated area, isolated from incompatible substances such as oxidizers and strong acids. Use secondary containment to prevent leaks, and label all storage containers clearly. Follow all local regulations and safety protocols for hazardous chemicals.
    Application of N-Methyl-2-(Trifluoromethoxy)Aniline

    Applications of N-Methyl-2-(Trifluoromethoxy)Aniline in Industrial Manufacturing

    As a direct manufacturer with longstanding expertise in fine chemical synthesis, we supply N-Methyl-2-(Trifluoromethoxy)Aniline to a select group of downstream industries, where it functions as a critical intermediate or specialty additive. Below we detail genuine industrial applications that integrate this compound, including use requirements, technical handling, and the standards that govern our clients’ formulations.

    1. Agrochemical Active Ingredient Synthesis

    Agrochemical producers utilize N-Methyl-2-(Trifluoromethoxy)Aniline as a key building block for the synthesis of herbicide and fungicide actives exhibiting enhanced metabolic stability and foliage uptake. This compound introduces both methylamino and trifluoromethoxy functional groups that support the design of target-specific pesticides. For custom synthesis, formulators adjust the input ratio based on the structure–activity relationship results and final active load requirements. Our QC procedures align shipment batches with established purity and moisture control guidelines under the pressure of tight crop protection regulatory authorizations.

    Industry compliance standards

    • ISO 9001:2015 Quality Management System
    • FAO/WHO Specifications for Plant Protection Products
    • OECD Principles of Good Laboratory Practice (GLP) for active ingredient manufacturing
    • National regulatory registration protocols (EPA, EU REACH, China ICAMA)

    Typical usage ratio

    • Usually 0.05–0.3 molar equivalents in multi-step active substance synthesis; adjusted according to target molecule design and downstream process efficiency

    Downstream process integration

    • Introduced at the condensation or coupling stage during heterocyclic ring construction, prior to chlorination, nitration, or further derivatization steps

    Final product types

    • Technical-grade agrochemical actives (e.g., aryl anilide, phenoxy herbicides)
    • Suspension concentrates and emulsifiable concentrates after post-processing
    • Pre-formulated granules for localized field application

    2. Pharmaceutical Intermediate for Small Molecule Synthesis

    Process chemists employ N-Methyl-2-(Trifluoromethoxy)Aniline as an advanced intermediate during the manufacture of certain fluorinated pharmacophores, including kinase inhibitors and neuroactive substance candidates. The compound’s unique substitution pattern favors increased receptor binding and metabolic longevity. For cGMP-compliant production, downstream partners incorporate the material under validated conditions and perform trace impurity clearance in subsequent purification. Documentation and traceability from our facility support every shipment as per DMF and site-audit requirements.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • US FDA cGMP 21 CFR Part 211
    • European Pharmacopoeia (Ph. Eur.) for reference substance purity
    • Drug Master File (DMF) support for regulatory submission

    Typical usage ratio

    • Introduced at 0.8–1.2 equivalents relative to halogenated core substrates, proportion adjusted based on reaction yield and process scale

    Downstream process integration

    • Applied at nucleophilic aromatic substitution or amination stages; further processed through protection, deprotection, and oxidative cyclization steps

    Final product types

    • Advanced pharmaceutical intermediates
    • APIs for oncology, CNS, and anti-infective preparations
    • Reference standards in preclinical drug discovery

    3. Organic Electronic Material Precursor

    Manufacturers of high-performance functional materials—specifically, suppliers for OLED and organic transistor production—utilize N-Methyl-2-(Trifluoromethoxy)Aniline as a monomer or substituent in creating electron transport layers and emissive compounds. Its electron-donating and fluoroalkoxy properties contribute to improved device voltage thresholds and operational lifetimes. Batch control focuses on metal cation content and by-product removal, responding to material purity standards that directly affect end-use electronic performance.

    Industry compliance standards

    • IEC 60068-2-20 Environmental Testing for Electronic Materials
    • RoHS Directive (EU 2015/863) for hazardous substance content
    • ISO 14001:2015 Environmental Management Standards
    • QMS documentation traceability for high-purity fine chemicals

    Typical usage ratio

    • 2–7% by weight in organic synthesis feedstock formulation, based on the desired polymer backbone or electronic layer function

    Downstream process integration

    • Inserted during polymerization or co-monomer addition for the formulation of small-molecule and polymeric organic semiconductors

    Final product types

    • OLED emissive and charge transport materials
    • Flexible display pixel inks
    • Organic field-effect transistor layers

    4. Specialty Dyestuff Manufacturing

    Producers in the dye and pigment sector incorporate N-Methyl-2-(Trifluoromethoxy)Aniline for creating high-performance arylamine-based colorants. The fluorinated structure enhances lightfastness, solvent resistance, and thermal durability for demanding industrial textile and plastics applications. Our production emphasizes batch reproducibility in line with colorimetric and fastness requirements specified by major downstream integrators.

    Industry compliance standards

    • OEKO-TEX® Standard 100 for textile safety
    • EN 71-3:2019 for pigment use in toys and plastics
    • DIN ISO 105-B02 for color fastness to light
    • REACH Annex XVII for restricted substances in dyes

    Typical usage ratio

    • 1.5–6% by mass in diazo-coupling or oxidative dye precursor synthesis, determined by target shade and fastness profile

    Downstream process integration

    • Introduced during the azo coupling or condensation step; processed further for sulfonation or mixed-metal complexation when required

    Final product types

    • High-performance dyestuff for polyester and cellulosic fibers
    • Solvent dyes for plastics and engineering resins
    • Pigment dispersions in automotive and industrial coatings
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