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HS Code |
568141 |
| Productname | 3-Bromo-1,1,1-Trifluoropropane |
| Casnumber | 460-41-7 |
| Molecularformula | C3H4BrF3 |
| Molecularweight | 178.96 |
| Appearance | Colorless liquid |
| Boilingpoint | 76-78°C |
| Density | 1.581 g/mL at 25°C |
| Refractiveindex | 1.358 |
| Meltingpoint | -63°C |
| Solubility | Insoluble in water |
| Purity | Typically >=98% |
| Synonyms | 1,1,1-Trifluoro-3-bromopropane |
| Smiles | C(CBr)C(F)(F)F |
| Inchikey | OAGXHTOMHYVWEU-UHFFFAOYSA-N |
As an accredited 3-Bromo-1,1,1-Trifluoropropane factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 3-Bromo-1,1,1-Trifluoropropane is supplied in a 100 mL amber glass bottle with a secure screw cap and hazard labeling. |
| Shipping | 3-Bromo-1,1,1-Trifluoropropane is shipped as a hazardous material, typically in sealed, UN-approved containers to prevent leaks or exposure. The chemical is transported under regulated conditions, following all relevant safety, labeling, and documentation standards as required for flammable, toxic, or halogenated organic compounds. Proper handling and storage guidelines must be observed. |
| Storage | 3-Bromo-1,1,1-Trifluoropropane should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from sources of ignition, heat, and direct sunlight. Keep separate from strong oxidizing agents. Store at room temperature, but avoid excessive moisture. Use secondary containment to prevent leaks or spills, and ensure appropriate labeling in accordance with safety regulations. |
Applications of 3-Bromo-1,1,1-Trifluoropropane in Industrial Manufacturing3-Bromo-1,1,1-Trifluoropropane acts as a key building block in several specialized chemical industries. As the original manufacturer, we maintain traceable quality control throughout each process step to meet high downstream demands. The following sections present actual industrial application segments with verified regulatory and process specifics. 1. Synthesis of Fluorinated Agrochemical IntermediatesSeveral manufacturers in the agrochemical field use this compound to introduce trifluoromethyl groups in syntheses for advanced technical active molecules. Its reactivity allows controlled substitution in multi-step organic synthesis for generating herbicide and insecticide intermediates. Integration typically occurs during the halogen-exchange stage or in nucleophilic substitution reactions under controlled parameters and inert atmospheres to minimize byproduct formation. Process engineers manage reagent ratios and temperature profiles to ensure regulatory compliance for environment and worker safety. Industry compliance standards
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2. Pharmaceutical Intermediate Synthesis (API Route Development)Custom synthesis of pharmaceutical intermediates often uses this compound to construct trifluoromethyl-containing side chains for select APIs in cardiovascular, CNS, and antiviral therapy candidates. The compound typically reacts under anhydrous conditions to minimize side-reactions, and batch records comply with GMP process documentation. Reaction scale, purity, and traceability remain critical from gram-scale pilot runs to full industrial campaigns. Cold chain management applies where product stability requires. Industry compliance standards
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3. Key Intermediate in Fire Suppressant Gas ManufactureProducers employ this material as a critical precursor in synthesizing next-generation halogenated fire extinguishing agents, especially for clean agent gas blends. The process involves stepwise halogen-exchange and fluorination, meeting stringent purity requirements to limit residual brominated by-products. Reactors feature specialist materials for corrosion resistance. Gas handling SOPs reference hazardous substances management under respective regional guidelines, and continuous in-line GC testing manages blending accuracy. Industry compliance standards
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4. Sourcing Agent in Advanced Polymer ModificationProducers of specialty fluorinated polymers and copolymers rely on this chemical as a sourcing agent for introducing short-chain trifluoropropyl units during free-radical or ionic polymerization. Its precise introduction influences polymer flexibility, chemical inertness, and dielectric properties. The addition occurs under regulated conditions, using specific initiators and temperature programs. Residual monomer control and solvent recovery form part of standard QC, as does the analysis of final polymer composition by NMR and FTIR techniques. Industry compliance standards
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5. Precursor for Specialty Fluorinated SolventsChemical formulators utilize this substance as a starting material in the creation of specific fluorinated solvents tailored for electronics cleaning, dry etching, and precision degreasing. The downstream process includes sequential substitution and hydrodehalogenation, refining the product through distillation to meet high-purity specifications. Site operators rigorously track batch records for each solvent lot and maintain documentation for exposure and emissions control. Industry compliance standards
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