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HS Code |
412441 |
| Chemical Name | 3,5-Dichloro-4-(1,1,2,2-Tetrafluoroethoxy)Phenyl Isocyanate |
| Cas Number | 86404-63-9 |
| Molecular Formula | C9H2Cl2F4NO2 |
| Molecular Weight | 306.02 g/mol |
| Appearance | Colorless to pale yellow liquid |
| Purity | Typically >98% |
| Synonyms | Isocyanic acid, 3,5-dichloro-4-(1,1,2,2-tetrafluoroethoxy)phenyl ester |
| Smiles | C1=C(C=C(C(=C1Cl)OCC(F)(F)C(F)F)Cl)N=C=O |
| Storage Conditions | Store in a cool, dry, and well-ventilated place |
| Solubility | Reacts with water |
As an accredited 3,5-Dichloro-4-(1,1,2,2-Tetrafluoroethoxy)Phenyl Isocyanate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle, 25g; tightly sealed with Teflon-lined cap, labeled with hazard warnings and chemical identification, protective outer carton. |
| Shipping | 3,5-Dichloro-4-(1,1,2,2-Tetrafluoroethoxy)Phenyl Isocyanate should be shipped in tightly sealed, chemical-resistant containers under cool, dry conditions. It must be labeled as a hazardous material (isocyanate, toxic, irritant) and handled by trained personnel in accordance with all applicable transportation regulations (e.g., DOT, IATA, IMDG). Avoid heat, moisture, and incompatible substances. |
| Storage | Store **3,5-Dichloro-4-(1,1,2,2-tetrafluoroethoxy)phenyl isocyanate** in a tightly sealed container under a dry, inert atmosphere such as nitrogen. Keep away from moisture, heat, and direct sunlight in a cool, well-ventilated area. Segregate from water, alcohols, strong acids, and bases. Use proper chemical labeling, and ensure access to spill kits and appropriate personal protective equipment nearby. |
Applications of 3,5-Dichloro-4-(1,1,2,2-Tetrafluoroethoxy)Phenyl Isocyanate in Industrial Manufacturing3,5-Dichloro-4-(1,1,2,2-Tetrafluoroethoxy)Phenyl Isocyanate serves as a critical intermediate in the synthesis of specialty polymers and advanced performance coatings. Its unique reactivity profile allows precise integration into downstream formulations that require elevated chemical resistance, thermal stability, and specific fluorinated characteristics. Below we detail major industrial application tracks, including compliance standards, practical usage ratios, process integration points, and examples of final goods. 1. Fluorinated Polyurethane Elastomers for Harsh Chemical EnvironmentsLeading manufacturers incorporate this isocyanate into the prepolymer step during fluorinated polyurethane elastomer production for environments with aggressive solvent exposure or caustic chemical contact. The molecule’s electron-withdrawing substituents and isocyanate group enable high-density crosslink formation, featuring exceptional resistance to swelling and thermal degradation. Its use supports applications ranging from pump diaphragms to advanced sealing components that face sustained exposure to oils, fuels, or acids. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
2. Specialty Fluorinated Urethane Coatings for Electronics and AerospaceCoatings producers use the compound as a building block in high-performance urethane topcoats and conformal coatings. Its presence delivers strong barrier properties against moisture, aggressive solvents, and temperature cycling. The isocyanate reacts with polyols containing additional fluorinated groups to generate a cured film exhibiting low surface energy, minimizing contaminant adhesion and dielectric loss. Such coatings serve protective and longevity functions in PCB assemblies, avionics housings, and critical connector seals. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
3. Synthesis of Fluorinated Agrochemical IntermediatesAs a manufacturer, we supply this isocyanate as a core intermediate in agrochemical actives synthesis where controlled isocyanate reactivity and fluorine incorporation are required. Its aromatic backbone and electron-deficient profile support the efficient construction of urea, carbamate, or amide linkages via nucleophilic substitution reactions. This approach allows agrochemical formulators to develop actives featuring enhanced weatherability and resistance to metabolic breakdown while meeting stringent environmental and toxicological demands. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
4. High-Performance Fluorinated Block Copolymers for Membrane ManufacturingPolymer industry clients use this isocyanate to construct block copolymers that combine fluorinated and urethane segments for advanced membrane fabrication. The specific structure delivers precise control over molecular architecture, enabling tunable hydrophobicity, ion selectivity, and resistance to fouling in filtration media. This approach supports applications in membrane separation for pharmaceuticals, semiconductor ultrapure water systems, and industrial waste treatment plants where durability and selectivity are critical. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
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