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4-Fluoro-3-(Trifluoromethyl)Anisole

    • Product Name 4-Fluoro-3-(Trifluoromethyl)Anisole
    • Alias 4-Fluoro-3-(trifluoromethyl)anisole
    • Einecs 411-280-8
    • 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

    106213

    Productname 4-Fluoro-3-(Trifluoromethyl)Anisole
    Casnumber 261762-33-2
    Molecularformula C8H6F4O
    Molecularweight 194.13
    Appearance Colorless to pale yellow liquid
    Boilingpoint 127-129°C (at 15 mmHg)
    Density 1.358 g/cm³
    Refractiveindex n20/D 1.443
    Purity Typically ≥98%
    Solubility Insoluble in water; soluble in organic solvents
    Synonyms 4-Fluoro-3-(trifluoromethyl)anisole, 1-Methoxy-2-fluoro-5-(trifluoromethyl)benzene
    Smiles COC1=CC(=CC(=C1)F)C(F)(F)F
    Inchikey RUOLZBPLCCHKJY-UHFFFAOYSA-N

    As an accredited 4-Fluoro-3-(Trifluoromethyl)Anisole factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle, tightly sealed with screw cap, labeled with hazard symbols and details; contains 25 grams of 4-Fluoro-3-(Trifluoromethyl)Anisole.
    Shipping 4-Fluoro-3-(Trifluoromethyl)Anisole is shipped in tightly sealed containers designed to prevent leaks or contamination. The chemical is transported under ambient conditions, following standard safety protocols for handling organic compounds. Packaging complies with relevant regulations to ensure secure delivery, proper labeling, and protection from moisture, heat, and direct sunlight during transit.
    Storage Store **4-Fluoro-3-(Trifluoromethyl)anisole** in a tightly closed container, in a cool, dry, and well-ventilated area away from incompatible substances such as strong oxidizers. Protect from heat, moisture, and direct sunlight. Use non-sparking tools and proper grounding to prevent static discharge. Ensure access to spill containment materials and appropriate personal protective equipment in storage areas.
    Application of 4-Fluoro-3-(Trifluoromethyl)Anisole

    Applications of 4-Fluoro-3-(Trifluoromethyl)Anisole in Industrial Manufacturing

    As a direct manufacturer, we supply 4-Fluoro-3-(Trifluoromethyl)Anisole to a range of specialized industrial sectors. This compound enables complex organic synthesis steps in pharmaceutical, agrochemical, and advanced material applications, where strict quality control, safety guidelines, and precise technical parameters guide its use.

    1. Pharmaceutical Intermediate Synthesis

    Pharmaceutical companies incorporate this compound to construct key aromatic intermediates in active pharmaceutical ingredient (API) synthesis for small molecule drugs, especially in the preparation of fluorinated benzenoid scaffolds. Batch protocols require exact charge timing and reaction parameters, including temperature and solvent conditions, to meet consistency needs. The downstream process emphasizes strict impurity profiling and successful crystallization at scale, ensuring the highest purity intermediates that comply with global registration requirements.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice Guideline
    • U.S. FDA 21 CFR Part 210/211
    • European Pharmacopoeia (Ph. Eur.) quality controls for APIs
    • Chinese Pharmacopoeia (ChP) process requirements

    Typical usage ratio

    • 10-25 mol% relative to primary starting materials, adjusted according to target API structure and reaction scale

    Downstream process integration

    • Charged during aromatic substitution, halogen-metal exchange, or etherification steps
    • Feeds directly into multi-step synthesis chains before heterocycle formation or further fluorination

    Final product types

    • Fluorinated API intermediates
    • Custom-developed drug precursors
    • Final APIs for oncology and CNS therapeutics

    2. Agrochemical Active Ingredient Development

    Agrochemical formulators use this raw material in the production of fluorinated phenolic building blocks during the synthesis of novel herbicides and fungicides. The compound participates in substitution reactions that create molecular backbones resistant to degradation and environmental breakdown. R&D and pilot batches must reconcile strict purity targets with minimized byproduct formation, while large-scale integration relies on precise, validated process flows.

    Industry compliance standards

    • FAO/WHO Good Laboratory Practice (GLP)
    • OECD Guidelines for Testing of Chemicals
    • ISO 9001:2015 certified QC systems
    • REACH Regulation (EC) No 1907/2006 pre-registration for raw material supply

    Typical usage ratio

    • 5-18% by weight per batch, depending on the required fluorine incorporation level of the end compound

    Downstream process integration

    • Incorporated via aromatic nucleophilic substitution in building block synthesis
    • Feeds into coupling steps with heterocycles or sulfonamides for product finalization

    Final product types

    • Active ingredients for pre- and post-emergence herbicides
    • Fungicidal scaffolds with improved field stability
    • Intermediate stocks for further crop protection molecule synthesis

    3. Liquid Crystal Display (LCD) Material Manufacturing

    Electronic materials producers utilize the compound to introduce fluorinated aromatic residues during the synthesis of specialty anisole derivatives for LCD alignment layers and related substrates. The material's physicochemical properties support precise tuning of dielectric and viscosity parameters required in modern display architectures. Processing stages demand tight handling controls to prevent contamination and ensure even distribution within high-purity material streams.

    Industry compliance standards

    • RoHS Directive (2011/65/EU) hazardous substance rules
    • IEC 61249 series for base materials quality
    • ISO 14644 Cleanroom Standards for processing lines
    • JPCA-ES-01 for electrical substrate validation

    Typical usage ratio

    • 3-8% by molecular fraction within precursor blends, modifiable based on end-device design requirements

    Downstream process integration

    • Inserted during the synthesis of precursor monomers for polyimide coatings
    • Feeds into blending tanks before application to glass substrates in vacuum environments

    Final product types

    • Polyimide-based LCD alignment coatings
    • Specialty liquid crystal monomers
    • Display substrate surface modifiers

    4. Organic Semiconductor Material Synthesis

    Producers of organic semiconductors select this compound as a functionalized building block during the development of small-molecule semiconducting materials. Its incorporation enables the tuning of electron affinity and molecular packing in thin-film device precursors. The process requires clean conditions and accurate measurement, supporting reproducible electron transport properties in the resulting films and devices. Each production lot undergoes full documentation for traceability and batch-to-batch qualification.

    Industry compliance standards

    • IEC 60068 environmental testing for electronic materials
    • ISO 14001 environmental management
    • Internal customer-required purity specifications (≥99.5%)
    • RSL (Restricted Substances List) for semiconductor fabs

    Typical usage ratio

    • 5-14 wt% in organic small-molecule semiconductor precursor formulations, optimized per device design

    Downstream process integration

    • Charged during Friedel–Crafts acylation, Suzuki couplings, or Stille reactions for precursor extension
    • Forms part of final monomer structure before solution processing or vacuum deposition

    Final product types

    • Organic light-emitting diode (OLED) emissive materials
    • Organic field-effect transistor (OFET) layers
    • Thin-film photovoltaic absorber materials

    5. Specialty Fluorinated Polymer Additive Production

    Producers incorporate this raw material into the synthesis routes for high-performance fluorinated polymer additives, targeting increased chemical resistance and thermal stability in engineering plastics. Reactions employ this compound as a functional monomer or chain-terminating agent, supporting precise control over polymer microstructure. Operations use dedicated reactors with inert gas blanketing to prevent introduction of cross-contaminants and achieve the specification targets demanded by downstream automotive and electronics applications.

    Industry compliance standards

    • UL 94 Flammability Standard for Plastics
    • ISO 10993-5 for biocompatibility (where relevant)
    • ASTM D638 tensile property testing for plastics
    • Automotive OEM raw material approval lists (e.g., VW TL, GM MAT)

    Typical usage ratio

    • 2-10 mol% within copolymerization feed composition, adjusted for desired performance enhancement

    Downstream process integration

    • feeds into copolymerization or terpolymerization steps with fluoroalkene or ether monomers
    • introduced prior to chain propagation or molecular weight regulation reactions

    Final product types

    • Fluorinated polymer flow modifiers
    • Anti-drip additives for high-heat plastics
    • Coatings for wire insulation materials

    6. Medicinal Chemistry R&D Support

    Medicinal chemists in drug discovery laboratories employ this compound in fragment-based lead finding and structure-activity relationship (SAR) optimization projects. The molecule acts as a specialized substituent in creating libraries of fluorinated analogues for automated biological screening pipelines. Lab scale synthesis protocols prioritize small batch reproducibility and spectroscopic purity, with records supporting GLP traceability and documentation for international patent claims.

    Industry compliance standards

    • OECD Principles of Good Laboratory Practice (GLP)
    • USP General Chapter <1058> Analytical Instrument Qualification
    • ISO/IEC 17025 certification for analytical labs
    • Patent filing documentation per WIPO PCT

    Typical usage ratio

    • 0.5-3 equivalents in parallel reaction arrays, scaled according to screening throughput

    Downstream process integration

    • charged into combinatorial synthesis loops for aryl ether diversification
    • integrated before functional group interconversion or protection/deprotection sequences

    Final product types

    • Probe compounds for in vitro target binding
    • Lead series for preclinical candidate nomination
    • Annotated compound libraries for SAR evaluation
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