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1,1-Dibromo-3,3,3-Trifluoroacetone

    • Product Name 1,1-Dibromo-3,3,3-Trifluoroacetone
    • Einecs 252-188-2
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    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 & Storage
    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.
    Application of 1,1-Dibromo-3,3,3-Trifluoroacetone

    Applications of 1,1-Dibromo-3,3,3-Trifluoroacetone in Industrial Manufacturing

    1,1-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 Synthesis

    This 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

    • ICH Q7 Good Manufacturing Practice for APIs
    • US Pharmacopeia (USP) monographs where applicable
    • EU EudraLex Vol 4 GMP for active substances
    • REACH registration for intermediate use

    Typical usage ratio

    • Applied at 1–10 mol% in key condensation or cyclization steps, adjusted per route design and impurity profile

    Downstream process integration

    • Introduced during protected group addition, arylation, or as a coupling agent in early to mid-stage batch synthesis, prior to final API formation

    Final product types

    • Active Pharmaceutical Ingredients (APIs) for advanced therapeutics
    • Regulatory drug substance intermediates
    • Clinical trial sample substances

    2. Agrochemical Active Ingredient Development

    Many 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

    • OECD Good Laboratory Practice (GLP) for development phase
    • FAO/WHO specifications for pesticide intermediates
    • EPA TSCA regulation for chemical intermediates
    • REACH SVHC screening if exceeding certain quantities

    Typical usage ratio

    • Often used at 2–15% w/w of total batch, adjusted based on multi-step route yield and crop protection profile

    Downstream process integration

    • Fed into heterocycle construction, halogen-exchange, or trifluoromethylation steps, typically at the pre-final active stage

    Final product types

    • Herbicide and pesticide actives with trifluoromethyl-bromo chemotypes
    • Intermediate compounds for regulated crop protection agents
    • Seed treatment formulation precursors

    3. Specialty Fluorinated Polymer Synthesis

    Chemical 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

    • ASTM D4066 for fluoropolymer material quality
    • UL 94 standards for flammability of plastic parts
    • IEC 61249-2-21 for non-halogenated and F-content PCB materials
    • ISO 9001:2015 for process management and traceability

    Typical usage ratio

    • Ratio of 0.5–5% of total monomer content, depending on polymer architecture and desired flame-retardant rating

    Downstream process integration

    • Added during pre-polymerization, as chain transfer agent, or in controlled radical copolymerization reactors

    Final product types

    • Fluorinated copolymer pellets for wire insulation
    • Printed circuit board laminate resins
    • Flame-retardant films and sheets for electronics

    4. Analytical Derivatization Reagents Production

    Specialty 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

    • ISO 17034 for reference material producers
    • USP Chapter <621> Chromatography
    • ISO/IEC 17025 for analytical laboratory traceability
    • EN 17036 for chemical reference materials

    Typical usage ratio

    • Typically formulated at 0.1–5% (w/v) in proprietary derivatization kit solutions, per analyte and sensitivity needs

    Downstream process integration

    • Utilized in reagent manufacturing during the labeling or tagging step to enhance analytical compound detectability

    Final product types

    • GC/LC derivatization reagent kits
    • Calibration standards for trace analysis
    • Reference tagging agents for dioxin and pesticide quantification

    5. Organofluorine Fine Chemical Manufacturing

    Producers 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

    • ISO 9001:2015 quality system standard
    • Toll manufacturing agreements with specification sheets
    • REACH registration for industrial intermediates
    • Transportation per IMDG/ADR for hazardous goods

    Typical usage ratio

    • Commonly 0.5–10% molar equivalent, adjusted to process step and downstream conversion yield requirements

    Downstream process integration

    • Deployed in targeted electrophilic bromination step, or as a coupling partner for aryl and alkylation reactions in catalytic flows

    Final product types

    • Organofluorine precursors for electronic specialty chemicals
    • Novel ligands for transition metal catalysis
    • Fluorinated dye intermediates
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