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2-(Trifluoromethoxy)Nitrobenzene

    • Product Name 2-(Trifluoromethoxy)Nitrobenzene
    • Alias 2-nitrophenyl trifluoromethyl ether
    • Einecs 237-619-9
    • 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

    286794

    Chemicalname 2-(Trifluoromethoxy)Nitrobenzene
    Casnumber 320-50-3
    Molecularformula C7H4F3NO3
    Molecularweight 207.11
    Appearance Pale yellow liquid
    Boilingpoint 215-217°C
    Meltingpoint -1°C
    Density 1.505 g/cm3
    Refractiveindex 1.509
    Solubility Insoluble in water; soluble in organic solvents
    Flashpoint 87°C
    Purity Typically ≥98%

    As an accredited 2-(Trifluoromethoxy)Nitrobenzene 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 25 grams of 2-(Trifluoromethoxy)nitrobenzene, sealed with a screw cap and labeled with hazard warnings.
    Shipping **Shipping Description:** 2-(Trifluoromethoxy)Nitrobenzene should be shipped in tightly sealed containers, away from incompatible substances and sources of ignition. Use appropriate labeling indicating hazardous material. Typically, it is transported as a limited quantity under UN 2810 (Toxic Liquid, Organic, N.O.S.), following all relevant chemical shipping and safety regulations.
    Storage 2-(Trifluoromethoxy)nitrobenzene should be stored in a tightly closed container in a cool, dry, and well-ventilated area, away from heat, sparks, open flames, and incompatible substances such as strong oxidizers and reducing agents. Protect from direct sunlight and moisture. Ensure proper labeling, and handle with gloves and eye protection to prevent skin and eye contact.
    Application of 2-(Trifluoromethoxy)Nitrobenzene

    Applications of 2-(Trifluoromethoxy)Nitrobenzene in Industrial Manufacturing

    2-(Trifluoromethoxy)Nitrobenzene serves as a high-purity intermediate in several advanced chemical manufacturing streams. Our direct manufacturing and strict in-house quality controls ensure consistent supply for demanding industrial applications. Below, we detail established downstream uses, with specific reference to industry regulations, proportional use, technical processing, and finished product categories.

    1. Agrochemical Synthesis: Selective Herbicide Intermediates

    This compound plays a key role as an electrophilic aromatic substitution intermediate for synthesizing selective pre- and post-emergence herbicides. It enables the production of fluorinated oxyaryl derivatives, which offer improved weed control in cereal and broadleaf crop protection. Downstream manufacturers use this intermediate to develop active ingredients meeting strict regional regulations.

    Industry compliance standards

    • OECD guidelines for the Testing of Chemicals
    • EU Regulation (EC) No 1107/2009 concerning the placing of plant protection products on the market
    • China Ministry of Agriculture National Pesticide Registration
    • US FIFRA (Federal Insecticide, Fungicide, and Rodenticide Act)

    Typical usage ratio

    • 5–15% weight-to-weight as a key advanced intermediate, with adjustments based on target herbicide formulation and substitution pattern requirements

    Downstream process integration

    • Introduced during the aromatic nucleophilic or palladium-catalyzed amination stage in multi-step synthesis of target herbicidal actives
    • Supports building of final oxyphenoxy, triazine, or pyridine-based compounds
    • Plays a structural role where trifluoromethoxy group expansion is needed for activity spectrum

    Final product types

    • Commercialized crop protection agents (herbicide technical concentrates)
    • Formulated granular and liquid herbicide end-use products
    • Custom blended pre-mix plant protection solutions for industrial agriculture

    2. Pharmaceutical API Intermediate: Fluorinated Anti-inflammatory Agents

    It acts as a starting building block in the multi-step production of specific anti-inflammatory drug APIs with high metabolic stability. Medicinal chemists prioritize the incorporation of trifluoromethoxy functionalities for improved bioavailability and efficacy in small-molecule research pipelines. Downstream partners use this intermediate for authorized synthesis routes requiring consistent analytical specifications.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • EU Pharmacopoeia monographs (where applicable for finished API)
    • US FDA 21 CFR Part 211 for finished pharmaceuticals
    • China Pharmacopoeia (volume II) for APIs

    Typical usage ratio

    • 3–10 mol% input relative to total batch, varying with synthetic route to final potent API and process yield optimization

    Downstream process integration

    • Utilized at aryl nitration coupling or direct reduction stage
    • Feeds into subsequent reduction and condensation, forming the core for advanced heterocyclic drugs
    • Requires analytical traceability per batch release records

    Final product types

    • Batch manufactured Active Pharmaceutical Ingredients (APIs) for anti-inflammatory indications
    • Column-purified intermediates for further small-molecule innovation
    • Chemical reference standards for pharmaceutical QC

    3. Electronic Chemical: High-Performance Liquid Crystal Monomers

    It is valued as an aromatic reagent in the design and development of fluorinated liquid crystal monomers for advanced display technologies. The presence of a trifluoromethoxy substituent enhances the dielectric anisotropy and chemical resistance required for next-generation LCD and OLED screens. Specialty electronic chemical manufacturers utilize this intermediate for precision modifications of terminal aromatic rings.

    Industry compliance standards

    • IEC 61340-5-1: Electrostatics standard for electronic materials
    • REACH Regulation (EC) No 1907/2006 for registration of new substances
    • RoHS Directive 2011/65/EU compliance for restricted hazardous substances
    • Industry-specific analytical purity >99.5% GC for electronic intermediates

    Typical usage ratio

    • 1–5 mol% as an end-capping or side chain functionalizer, controlled based on required phase transition temperature of final mixture

    Downstream process integration

    • Enters aromatic substitution or etherification reactions with flexible monomer frameworks
    • Contributes to molecular alignment and viscosity tuning of nematic and smectic phases
    • Goes through further hydrogenation and purification for optoelectronic-grade performance

    Final product types

    • High-end liquid crystal mixtures for flat-panel displays
    • Specialty fluorinated alignment agents for OLED manufacturing
    • Test batches for prototype display cell production by electronics OEMs

    4. Specialty Polymer Additive: Fluorinated Monomer for Engineering Plastics

    This compound finds application as a fluorinated aromatic monomer introduced into engineering plastic formulations to enhance chemical durability and hydrophobicity. Polymer manufacturers use it to tailor polymers for medical, automotive, and electronics housings that require high-temperature resistance and low surface energy.

    Industry compliance standards

    • ISO 9001:2015 for process and quality management
    • UL 94 flammability rating for polymeric materials
    • FDA 21 CFR 177.1010 for components in polymer contact with food (if applicable after full polymerization)
    • ASTM D638 for tensile strength of plastics

    Typical usage ratio

    • Up to 2% by weight as a co-monomer or modifier, adjusted for desired mechanical and surface properties in copolymer blends

    Downstream process integration

    • Participates in solution or suspension polymerization with other aromatic, aliphatic, or fluorinated co-monomers
    • Blended into extrusion or molding resins after reactive blending and compounding
    • Monitored for full incorporation via spectroscopic QC before scale-up

    Final product types

    • Medical device housings and precision parts
    • Electronics-grade protective casings and connectors
    • High-performance automotive underhood components
    • Special lubricating coatings for industrial machinery

    5. Advanced Dye and Pigment Synthesis: Fluorinated Benzene Derivatives

    It functions as a foundational substrate for synthesizing high-contrast and chemically stable specialty dyes and pigments, particularly where solvent resistance and light fastness are critical. Industrial users include manufacturers of solvent-based inks, specialty coatings, and security-marking systems.

    Industry compliance standards

    • EN 71-3 for toy safety related to colorants and pigments
    • ISO 2846 for colorant consistency in printing inks
    • China GB 18582-2020 for low-VOC coatings
    • REACH Annex XVII for restricted aromatic amines in colorants

    Typical usage ratio

    • 0.5–3 mol% as precursor or modifier, depending on final chromophore and application fastness requirements

    Downstream process integration

    • Feeds into diazotization, coupling, or nucleophilic aromatic substitution with chromophoric core structures
    • Undergoes further reduction and derivatization for targeted functional group installation
    • Ensures batch color uniformity through controlled reaction parameters

    Final product types

    • Solvent-resistant pigments for security printing
    • Specialty high-contrast marking inks for electronics and automotive parts
    • Weather-resistant outdoor coatings and finishes
    • Anti-counterfeiting dyes for packaging and branding
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