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HS Code |
518891 |
| Chemical Name | 2,5-Bis(Trifluoromethyl)Aniline |
| Molecular Formula | C8H5F6N |
| Molecular Weight | 229.12 g/mol |
| Cas Number | 328-84-7 |
| Appearance | White to off-white solid |
| Boiling Point | 198-200°C |
| Melting Point | 45-49°C |
| Density | 1.49 g/cm³ |
| Purity | Typically ≥98% |
| Solubility | Slightly soluble in water; soluble in organic solvents such as dichloromethane, ethanol |
| Smiles | C1=CC(=C(C=C1N)C(F)(F)F)C(F)(F)F |
| Inchi | InChI=1S/C8H5F6N/c9-7(10,11)5-1-2-6(15)4(3-5)8(12,13)14 |
| Refractive Index | 1.480 (predicted) |
| Storage Temperature | Store at 2-8°C |
| Flash Point | 106°C |
As an accredited 2,5-Bis(Trifluoromethyl)Aniline factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | A 25g amber glass bottle, tightly sealed with a white screw cap, labeled with hazard symbols and `2,5-Bis(Trifluoromethyl)Aniline` details. |
| Shipping | **Shipping Description for 2,5-Bis(Trifluoromethyl)Aniline:** This chemical should be shipped in tightly sealed containers, protected from light and moisture. Store in a cool, well-ventilated area, away from incompatible substances. Label all packaging according to relevant safety regulations. Consult the MSDS for transport classifications and specific hazard precautions prior to shipping. |
| Storage | 2,5-Bis(Trifluoromethyl)Aniline should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as oxidizers and acids. Protect from light and moisture. Ensure proper labeling and keep away from direct sunlight. Use appropriate chemical storage cabinets for hazardous organics and limit access to trained personnel. |
Applications of 2,5-Bis(Trifluoromethyl)Aniline in Industrial ManufacturingOur production of 2,5-Bis(Trifluoromethyl)Aniline serves as a critical intermediate across several high-value industrial sectors. As a direct manufacturer, we support downstream companies implementing this fluorinated compound in advanced synthesis, specialty coatings, pharmaceutical research, and agrochemical development. 1. Advanced Pharmaceutical IntermediatesPharmaceutical manufacturers employ 2,5-Bis(Trifluoromethyl)Aniline when designing and scaling up small-molecule drug candidates requiring enhanced metabolic stability and fluorine incorporation at specific ring positions. It is mainly used in the synthesis of next-generation kinase inhibitors, CNS drug scaffolds, and API fluorination, where the electron-withdrawing effect of trifluoromethyl improves pharmacokinetic profiles and target selectivity. Integration into multi-step organic synthesis typically takes place during amidation, urea coupling, or as a nucleophilic aromatic substitution partner. Industry compliance standards
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2. Synthesis of Agrochemical Active CompoundsLeading agrochemical producers use this aniline derivative as a fluorine source in the synthesis of novel herbicides, insecticides, and fungicides. Its trifluoromethyl groups enhance the bioactivity and environmental stability of pyridine and quinoline rings, commonly found in crop protection agents. The compound features in key steps such as selective amination and ring closure reactions, supporting the design of active molecules with improved resistance to degradation, allowing better crop safety and regulatory compliance. Industry compliance standards
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3. Fluorinated Polymer SynthesisSpecialty polymer producers adopt this compound to design high-performance fluorinated aromatic polymers aimed at demanding electronic, aerospace, and membrane applications. The presence of two trifluoromethyl groups provides rigidity to the polymer backbone, increases thermal and chemical resistance, and improves dielectric properties. This material is introduced during the polycondensation or polyaddition reaction, mainly for forming high-grade polyimides, polyamides, and specialty fluoropolymers with controlled molecular weight distribution. Industry compliance standards
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4. Electronics Specialty CoatingsThe electronics sector leverages 2,5-Bis(Trifluoromethyl)Aniline in the formulation of specialty coatings where moisture barrier performance, dielectric strength, and chemical inertness are essential. Formulators use this raw material to synthesize advanced coating resins, such as fluorinated polyacrylate or polyimide varnishes, applied to semiconductors, high-voltage capacitors, and sensor units. The feedstock enters reaction sequences that require precise control of functional group distribution and batch purity to meet end-customer technical standards. Industry compliance standards
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5. Fine Chemical Synthesis & Custom Research ChemicalsContract research and fine chemical facilities procure 2,5-Bis(Trifluoromethyl)Aniline for the development of specialty intermediates, reference standards, and analytical markers required in life science, diagnostics, and material science applications. Due to its strong electron-withdrawing fluorinated groups, chemists select this compound for rapid screening of ring-substituted anilines during lead compound discovery, combinatorial chemistry, and in the generation of isotopically labeled standards for LC-MS quantification studies. Industry compliance standards
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