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HS Code |
970704 |
| Chemicalname | 1,1-Dibromo-3,3,3-trifluoroacetone |
| Casnumber | 431-47-0 |
| Molecularformula | C3Br2F3O |
| Molecularweight | 285.84 g/mol |
| Appearance | Colorless to pale yellow liquid |
| Density | 2.15 g/cm³ |
| Boilingpoint | 118-121°C |
| Meltingpoint | -8°C |
| Refractiveindex | 1.468 |
| Purity | Typically ≥98% |
| Synonyms | Dibromotrifluoroacetone; 1,1-dibromo-3,3,3-trifluoropropan-2-one |
| Flashpoint | 59°C (closed cup) |
| Smiles | C(=O)(C(C(F)(F)F)Br)Br |
| Inchikey | BNOBLFRNHMMUQT-UHFFFAOYSA-N |
As an accredited 1,1-Dibromo-3,3,3-Trifluoroacetone factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 1,1-Dibromo-3,3,3-Trifluoroacetone is supplied in a 25g amber glass bottle with a secure, chemical-resistant screw cap. |
| Shipping | **Shipping Description:** 1,1-Dibromo-3,3,3-Trifluoroacetone is shipped in tightly sealed glass bottles or compatible containers to prevent leaks. It must be kept cool, dry, and away from direct sunlight. Classified as hazardous, shipping requires proper labeling, UN identification, and adherence to all relevant local, national, and international transport regulations. |
| Storage | **1,1-Dibromo-3,3,3-Trifluoroacetone** should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from sources of ignition, heat, moisture, and incompatible substances such as strong bases and oxidizing agents. Store under inert atmosphere, such as nitrogen or argon, to prevent decomposition. Avoid exposure to light and handle inside a chemical fume hood. |
Applications of 1,1-Dibromo-3,3,3-Trifluoroacetone in Industrial Manufacturing1,1-Dibromo-3,3,3-Trifluoroacetone serves as a high-purity specialty intermediate in advanced chemical synthesis. Produced under controlled process conditions, this halogenated trifluoroacetone is supplied for use in specific regulated downstream sectors where strict consistency and traceability are required. Below we outline key industrial applications, technical integration considerations, and compliance standards observed in real manufacturing environments. 1. Pharmaceutical Intermediate SynthesisThis material is widely used as a key building block for developing fluorinated and brominated heterocycles in pharmaceutical API synthesis. Due to its bifunctional reactivity, it is selected in multi-step production sequences for oncology, anti-inflammatory, and CNS-active compounds, where halogenated ketone groups enhance molecule metabolism or receptor affinity. Processing requires close management of exposure and residuals to meet pharmacopeial purity, while maintaining traceability throughout validation scale-up. Industry compliance standards
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2. Agrochemical Active Ingredient DevelopmentMany pesticide and herbicide manufacturers employ this trifluoroacetone as an intermediate for producing next-generation fluorinated agrochemicals. Its electrophilic carbonyl structure enables efficient introduction of trifluoromethyl and brominated moieties into complex ring systems. Downstream sites often apply this compound under closed systems with dedicated containment due to volatile byproducts. Data on process and environmental fate are logged for compliance audits. Industry compliance standards
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3. Specialty Fluorinated Polymer SynthesisChemical process operators in the electronic and high-performance plastics industries utilize this material for introducing both bromine and trifluoromethyl groups into functionalized monomer units. Used primarily in the production of dielectric and flame-retardant polymer resins, it enters as a co-monomer or chain terminator, selected for applications requiring heightened resistance to heat, chemicals, and electrical stress. Batch records account for all residual monomer and decomposition products to meet precise specifications. Industry compliance standards
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4. Analytical Derivatization Reagents ProductionSpecialty chemical plants use this compound to prepare highly sensitive derivatization reagents for gas chromatography (GC), liquid chromatography (LC), and mass spectrometry (MS) analysis of trace organics. The dual halogen-fluoro motif greatly enhances detector response and separation for analytical labs checking pharmaceuticals, pesticides, and environmental samples. Quality systems mandate batch-to-batch identity confirmation and ultra-low impurity levels, with detailed documentation provided for each shipment batch. Industry compliance standards
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5. Organofluorine Fine Chemical ManufacturingProducers of custom organofluorine molecules incorporate this raw material as a multi-reactive node for the synthesis of advanced fine chemicals. It is critical in steps requiring selective introduction of trifluoromethyl and bromine functionalities into target molecules, leading to performance compounds in catalysis, high-stability ligands, and specialty colorants. Chemists design, monitor, and verify conversion rates and side-product formation to ensure consistency and compliance across each batch scale. Industry compliance standards
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