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HS Code |
712661 |
| Chemical Name | 4-Fluoro-2-(Trifluoromethyl)Benzamide |
| Cas Number | 328-75-6 |
| Molecular Formula | C8H5F4NO |
| Molecular Weight | 207.13 |
| Appearance | White to off-white solid |
| Melting Point | 102-106 °C |
| Purity | Typically ≥98% |
| Solubility | Soluble in organic solvents such as DMSO, DMF |
| Smiles | C1=CC(=C(C=C1F)C(=O)N)C(F)(F)F |
| Inchi | InChI=1S/C8H5F4NO/c9-5-2-1-4(8(10,11)12)3-6(5)7(13)14/h1-3H,(H2,13,14) |
As an accredited 4-Fluoro-2-(Trifluoromethyl)Benzamide factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle, 10 grams, tightly sealed with a screw cap, labeled with chemical name, CAS number, hazard symbols, and lot number. |
| Shipping | 4-Fluoro-2-(Trifluoromethyl)Benzamide is shipped in tightly sealed, chemical-resistant containers to prevent leakage and contamination. It is packed in accordance with international and local regulations for chemical transport, typically under ambient temperature. Proper labeling and documentation are included to ensure safe handling, compliance, and tracking during shipping. |
| Storage | Store 4-Fluoro-2-(trifluoromethyl)benzamide in a tightly sealed container, in a cool, dry, and well-ventilated area, away from incompatible substances such as strong oxidizing agents. Protect from direct sunlight and moisture. For safety, keep the chemical in a designated chemical storage cabinet and ensure proper labeling. Avoid exposure to heat and sources of ignition. |
Applications of 4-Fluoro-2-(Trifluoromethyl)Benzamide in Industrial ManufacturingAs a direct manufacturer of 4-Fluoro-2-(Trifluoromethyl)Benzamide, we supply this specialty intermediate to advanced industrial sectors requiring high-purity building blocks for complex synthesis. The following sections detail specific applications in regulated markets, technical use guidelines, and downstream integration in real-world manufacturing environments. 1. Agrochemical Intermediate for Fungicide SynthesisChemical companies utilize 4-Fluoro-2-(Trifluoromethyl)Benzamide as a key intermediate in the pathway of developing fluorinated aromatic fungicides. The molecule participates in acylation steps to introduce the necessary amide function, which contributes to biological activity. Formulators maintain strict trace impurity control to comply with export regulations for agrochemical actives. End products include triazole and strobilurin derivatives popular in crop protection. Industry compliance standards
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2. Pharmaceutical Intermediate for CNS Drug SynthesisPharmaceutical manufacturers employ this compound as an advanced intermediate for central nervous system (CNS) active pharmaceuticals. It acts as a fluorinated aromatic scaffold in the multi-step synthesis of benzamide-based anxiolytics and antipsychotics, ensuring defined regioselectivity and purity. Manufacturers adopt GMP-compliant QC measures throughout the API route, securing robust traceability and impurity control for regulatory filing. Industry compliance standards
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3. Specialty Chemical Production for OLED MaterialsDisplay technology developers incorporate this fluoro-substituted benzamide as a core building block for synthesizing rigid, electron-deficient aromatic units in organic light-emitting diode (OLED) materials. The controlled introduction of multiple electron-withdrawing groups enhances thermal stability and modifies energy levels of emitter materials. Producers operate under electronics-grade chemical purity requirements and document trace processing steps to ensure performance reproducibility in display fabrication. Industry compliance standards
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4. Raw Material for Fluorinated Polymer AdditivesProducers of specialty polymers integrate this benzamide derivative as a functional monomer or compatibilizing additive to enhance chemical resistance and modify surface energy in fluoropolymer-based blends. Typical applications target automotive coatings and protective films, demanding lot-to-lot consistency and validated dispersion performance in melt-processing. Formulators monitor crystal morphology and interfacial compatibility during compounding. Industry compliance standards
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5. Fine Chemical Feedstock for Advanced Dye SynthesisManufacturers of high-purity dyes and specialty colorants select 4-Fluoro-2-(Trifluoromethyl)Benzamide for its electron-withdrawing substituents, which impact solubility and fastness properties in final dye systems. It enters diazotization and subsequent coupling reactions, with trace-level anion contaminant control as per ultrapure dye requirements. Downstream QC focuses on color strength and stability for industrial inkjets and textile coloration. Industry compliance standards
Typical usage ratio
Downstream process integration
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