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HS Code |
987441 |
| Chemical Name | 4-(Trifluoromethylthio)Phenol |
| Cas Number | 827-98-5 |
| Molecular Formula | C7H5F3OS |
| Molecular Weight | 194.18 |
| Appearance | White to pale yellow crystalline powder |
| Melting Point | 55-59°C |
| Boiling Point | 109-111°C at 15 mmHg |
| Density | 1.49 g/cm3 |
| Refractive Index | n20/D 1.522 |
| Solubility | Slightly soluble in water, soluble in organic solvents |
| Smiles | C1=CC(=CC=C1O)SC(F)(F)F |
| Inchi | InChI=1S/C7H5F3OS/c8-7(9,10)12-6-3-1-5(11)2-4-6/h1-4,11H |
As an accredited 4-(Trifluoromethylthio)Phenol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Brown glass bottle, 25 grams, sealed with a secure cap; labeled with chemical name, hazard warnings, manufacturer's information, and batch number. |
| Shipping | 4-(Trifluoromethylthio)phenol is shipped in tightly sealed containers under cool, dry conditions, and protected from light and moisture. Classified as a hazardous material, it requires careful labeling and documentation. Appropriate personal protective equipment (PPE) and adherence to chemical transport regulations ensure safe handling during transit. |
| Storage | 4-(Trifluoromethylthio)phenol should be stored in a tightly sealed container, protected from light and moisture, and kept in a cool, well-ventilated area. Store away from incompatible substances such as strong oxidizers and bases. Ensure appropriate labeling, and follow all regulations for hazardous chemical storage. Use secondary containment to prevent spills and always wear suitable protective equipment when handling. |
Applications of 4-(Trifluoromethylthio)Phenol in Industrial Manufacturing4-(Trifluoromethylthio)Phenol serves specialized functions in several high-performance industrial production environments, where its unique physicochemical characteristics provide needed modifications in molecular structure. Our ongoing involvement with leading downstream manufacturers ensures stable product quality and regulatory compliance tailored to specific application demands. Below, we summarize the authentic industrial uses for this material, focusing on precise integration details relevant to process chemists, formulators, and production managers. 1. Advanced Agrochemical SynthesisDownstream agrochemical producers introduce 4-(Trifluoromethylthio)Phenol as a key intermediate in the manufacture of sulfur-containing phenoxy-based herbicides and fungicides. The electron-withdrawing trifluoromethylthio group increases target molecule stability and bioactivity, especially in actives formulated for resistance management. Production lines carefully meter the material to match reaction stoichiometry and control impurity profiles. Industry compliance standards
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2. Pharmaceutical Intermediate ProductionPharmaceutical API manufacturers use 4-(Trifluoromethylthio)Phenol as a building block in the synthesis of antithrombotic, anti-inflammatory, and central nervous system drug candidates involving fluorinated aromatic scaffolds. The compound's high reactivity and selective substitution facilitate late-stage functionalization in multi-step synthetic sequences. Accurate metering minimizes undesirable by-product formation compliant with current regulatory requirements for genotoxic impurities. Industry compliance standards
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3. High-Performance Polymer ModificationPolymers and specialty resin producers incorporate 4-(Trifluoromethylthio)Phenol to adjust hydrophobicity, chemical resistance, and electrical properties for performance materials used in electronics and coatings. The trifluoromethylthio functionality delivers targeted surface energy control and modifies cure kinetics during thermoset cross-linking. Adjustments to load level and process conditions enable manufacturers to balance final mechanical strength and insulation requirements. Industry compliance standards
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4. Custom Dye and Pigment ManufactureSpecialty dye and pigment producers deploy 4-(Trifluoromethylthio)Phenol in fine-tuned aromatic substitution and coupling reactions that enhance color depth, fastness, and solvent resistance in fluorinated pigment systems. The compound's high nucleophilicity enables efficient coupling to diazonium salts or during oxidative azo synthesis. Color chemists adjust usage based on target shade intensity and stability factors for high-value textile and plastics applications. Industry compliance standards
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