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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 | 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. |
Applications of 4-Fluoro-3-(Trifluoromethyl)Anisole in Industrial ManufacturingAs 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 SynthesisPharmaceutical 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
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2. Agrochemical Active Ingredient DevelopmentAgrochemical 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
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3. Liquid Crystal Display (LCD) Material ManufacturingElectronic 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
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4. Organic Semiconductor Material SynthesisProducers 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
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5. Specialty Fluorinated Polymer Additive ProductionProducers 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
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6. Medicinal Chemistry R&D SupportMedicinal 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
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