|
HS Code |
200747 |
| Chemical Name | Trifluoromethyl Iodide |
| Chemical Formula | CF3I |
| Molecular Weight | 195.91 g/mol |
| Cas Number | 2314-97-8 |
| Appearance | Colorless gas |
| Boiling Point | -21.8 °C |
| Melting Point | -110 °C |
| Density | 2.12 g/cm³ (at 0 °C) |
| Solubility In Water | Slightly soluble |
| Vapor Pressure | 2.09 atm (at 20 °C) |
As an accredited Trifluoromethyl Iodide factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Trifluoromethyl Iodide is packaged in a 100g amber glass bottle with a secure cap and warning labels for safety. |
| Shipping | Trifluoromethyl Iodide should be shipped in tightly sealed, corrosion-resistant containers, protected from light and moisture. It is classified as a hazardous material and must be transported according to relevant regulations, such as IATA or DOT requirements, with appropriate labeling and documentation to ensure safety during transit. Avoid heat and incompatible substances. |
| Storage | Trifluoromethyl iodide should be stored in a cool, dry, well-ventilated area away from direct sunlight and sources of heat or ignition. It must be kept in tightly sealed, corrosion-resistant containers, preferably made of materials compatible with halogenated compounds. Avoid contact with oxidizing agents. Proper labeling and secondary containment are essential to prevent leaks or accidental exposure. |
Applications of Trifluoromethyl Iodide in Industrial ManufacturingAs a direct manufacturer of Trifluoromethyl Iodide, we supply this specialized halogenating reagent to advanced industrial sectors with strict requirements for process safety, traceability, and regulatory conformity. The following sections detail its integration across major chemical production routes aligned with global regulatory standards. 1. Pharmaceutical Active Ingredient SynthesisGlobal pharmaceutical manufacturers use Trifluoromethyl Iodide as a key trifluoromethylation agent in the construction of complex active pharmaceutical ingredients (APIs). The reagent introduces trifluoromethyl groups into heterocyclic and aromatic compounds, directly impacting pharmacokinetics and metabolic stability. Chemical engineers incorporate it into one-pot or multi-step synthesis sequences under inert atmosphere, controlling stoichiometry tightly to maximize yield while complying with strict impurity profiles. The process demands accurate in-line monitoring and validated cleanroom handling to prevent cross-contamination. Finished API batches undergo full traceability documentation and batch release analytics per client specifications. Industry compliance standards
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2. Agrochemical Intermediate ProductionIndustrial agrochemical plants use this reagent to construct key intermediates for high-performance herbicides, fungicides, and insecticides. The compound’s selective trifluoromethyl group transfer enhances both biological activity and environmental persistence. Operators add it to halogen-exchange or arylation reactions under controlled temperature and solvent management, ensuring compatibility with downstream effluent treatment protocols. Application at this stage supports both technical-grade and formulated crop protection products, with dedicated ISO-certified quality assurance at each lot release. Industry compliance standards
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3. Specialty Fluorinated Polymer SynthesisProducers of high-performance fluoropolymers employ Trifluoromethyl Iodide as a monomer building block or radical initiator for the production of specialty elastomers and engineered materials. The reagent imparts unique chemical and thermal stability characteristics required for advanced cable sheathing, gaskets, and seals. Operators feed it into controlled polymerization reactors, often under high-vacuum and inert gas conditions, to ensure the precise integration of the trifluoromethyl moiety within the polymer backbone. Safety interlocks and gas phase containment are critical to protect operator health and maintain product purity. Industry compliance standards
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4. Advanced Material Surface ModificationManufacturers of semiconductor and technical textiles utilize Trifluoromethyl Iodide for controlled surface modification, aiming to enhance hydrophobicity and reduce surface energy. The material functions in plasma-phase or vapor-phase fluorination chambers, offering uniform functionalization of substrates such as silicon wafers, glass, or polymer sheets. Process engineers tightly regulate exposure time, chamber pressure, and reactant feed to maintain sharp distinction between treated and untreated regions. Final surfaces are validated for durability and chemical resistance according to electronic or textile performance standards. Industry compliance standards
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5. Fine Chemical and Specialty Intermediate ManufacturingProducers of fine chemicals and specialty intermediates rely on Trifluoromethyl Iodide to introduce fluorinated motifs in custom molecules, especially where demanding regulatory profiles or unique physicochemical behavior is required. These applications often involve contract manufacturing for electronics or specialty reagents, where product integrity, batch reproducibility, and comprehensive material data are required. Operators handle the reagent under high-purity conditions within sealed, validated vessels, employing precision metering and rigorous process audit trails. Formulation adjustments align with specificity of end-customer functional needs and international trade documentation. Industry compliance standards
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