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3-Phenyl-1,1,1-Trifluoropropan-2-One

    • Product Name 3-Phenyl-1,1,1-Trifluoropropan-2-One
    • Alias Phenyl Trifluoromethyl Ketone
    • Einecs 223-982-5
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry sales7@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    899557

    Chemical Name 3-Phenyl-1,1,1-Trifluoropropan-2-One
    Molecular Formula C9H7F3O
    Molecular Weight 188.15 g/mol
    Cas Number 116143-27-6
    Appearance Colorless to pale yellow liquid
    Boiling Point 68-70°C at 15 mmHg
    Density 1.235 g/mL at 25°C
    Refractive Index 1.450-1.454
    Smiles FC(F)(F)CC(=O)c1ccccc1
    Melting Point -3°C
    Solubility Slightly soluble in water; soluble in organic solvents
    Purity Typically ≥98%

    As an accredited 3-Phenyl-1,1,1-Trifluoropropan-2-One factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle containing 25 grams of 3-Phenyl-1,1,1-trifluoropropan-2-one, securely sealed, with hazard and handling labels.
    Shipping **Shipping Description:** 3-Phenyl-1,1,1-Trifluoropropan-2-One should be shipped in securely sealed containers, protected from moisture, heat, and direct sunlight. Use appropriate cushioning to prevent breakage. Label the package as a chemical substance and comply with relevant regulations regarding handling, transport, and documentation. Ensure that a safety data sheet (SDS) accompanies the shipment.
    Storage Store **3-Phenyl-1,1,1-trifluoropropan-2-one** in a tightly sealed container, in a cool, dry, and well-ventilated area away from sources of ignition and incompatible substances such as strong oxidizers and acids. Keep it away from direct sunlight and moisture. Use appropriate chemical storage cabinets, and ensure good labeling. Follow all local, state, and federal regulations for storage of organic chemicals.
    Application of 3-Phenyl-1,1,1-Trifluoropropan-2-One

    Applications of 3-Phenyl-1,1,1-Trifluoropropan-2-One in Industrial Manufacturing

    3-Phenyl-1,1,1-Trifluoropropan-2-One serves as a high-value intermediate in several advanced chemical manufacturing sectors, mainly in pharmaceutical synthesis, agrochemical formulation, fine fragrance compounds, and specialty material production. The following application scenarios represent direct, on-site uses by manufacturers who require precision in formulation, strict compliance, and consistent integration with their downstream processes.

    1. Active Pharmaceutical Ingredient Intermediate Synthesis

    Pharmaceutical companies incorporate this compound as a crucial building block during multi-step syntheses for various API molecules, especially those that utilize fluorinated aromatic ketones to promote metabolic stability and improve bioavailability profiles in final medicines. Its unique trifluoromethyl group selectively enhances the pharmacokinetic properties of several novel drug candidates, making it a preferred starting material for small-molecule drugs under development and commercial production pipelines.

    Industry compliance standards

    • Current Good Manufacturing Practice (cGMP) guidelines as outlined by the US FDA 21 CFR Part 210/211
    • ICH Q7: Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • Ph. Eur. (European Pharmacopoeia) monograph criteria for starting materials
    • Chinese Pharmacopoeia relevant purity and contaminant specifications

    Typical usage ratio

    • Used at 0.5% to 2.5% relative to the total synthesis batch, depending on target API yield and specific synthetic route steps

    Downstream process integration

    • Charged at the intermediate condensation or alkylation stage in multi-step API synthesis lines
    • Integrated with in-process QC checkpoints monitoring for ketone conversion and fluorine incorporation via HPLC and NMR

    Final product types

    • Fluorinated anti-inflammatory agents
    • Novel CNS (central nervous system) active ingredients
    • Experimental oncology drug molecules
    • Pipeline fluorinated intermediates for contract development manufacturing organizations (CDMOs)

    2. Agrochemical Active Ingredient Synthesis

    Manufacturers in the agrochemical industry utilize this raw material to introduce trifluoromethylated groups into active ingredient molecules, which can dramatically increase resistance to environmental degradation, sunlight, and microbial attack. These properties are essential for achieving high-performance protection in herbicides and fungicides, particularly those targeted for regions requiring robust field persistence.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • REACH Registration for EU market compliance
    • Environmental Protection Agency (EPA) Pesticide Registration process in the US
    • ISO 9001:2015 Quality Management Systems for agrochemical manufacturing

    Typical usage ratio

    • Introduced at 0.3% to 1.8% by mass within total synthetic batch, adjusted based on targeted molecule structure and field stability requirements

    Downstream process integration

    • Added during the fluorination or acylation stage in synthetic pesticide and herbicide pathways
    • Closely monitored by GC-MS for residual solvent and byproduct clearance in compliance with international technical grade standards

    Final product types

    • Trifluoromethylated fungicide actives for cereals and horticultural crops
    • Long-lasting herbicidal concentrates
    • High-value technical grade pesticide intermediates supplied to formulation plants

    3. Fragrance Ingredient for Fine Perfumes

    In the fragrance industry, this compound functions as a specialty ketone for synthesizing key aromatic building blocks that provide unique olfactory notes. Its chemical structure allows for formation of stable, high-impact intermediates in luxury perfume blends, contributing to distinctive, persistent fragrance signatures not achievable with conventional ketones.

    Industry compliance standards

    • IFRA (International Fragrance Association) Code of Practice
    • EU Cosmetics Regulation (EC) No 1223/2009
    • Cosmetic Ingredient Review (CIR) Expert Panel safety guidelines
    • ISO 9235: Aromatic natural raw materials – Vocabulary for fragrance compounds

    Typical usage ratio

    • Added at 0.05%–0.2% in core fragrance concentrate formulations, fine-tuned by perfumer based on required note intensity and blend compatibility

    Downstream process integration

    • Employed at the early synthesis phase to construct specialized aromatic intermediates prior to esterification or further derivatization
    • QC teams use GC/FID and mass spectrometry to ensure high purity ketone incorporation and absence of odor-impacting impurities

    Final product types

    • Luxury eau de parfum bases
    • Signature accords for niche fragrance houses
    • Stable fragrance intermediates exported to global blenders

    4. Fluorinated Specialty Polymer Precursors

    Advanced materials manufacturers employ this raw material as a component in the production of high-performance fluorinated polymers and copolymers, where its chemical backbone imparts enhanced chemical resistance, reduced polarity, and improved mechanical properties. This usage is common in precision electronics, coating materials, and select engineering plastics for demanding environments.

    Industry compliance standards

    • ISO 9001:2015 for industrial polymer synthesis
    • RoHS (Restriction of Hazardous Substances Directive) for electronics-related applications
    • REACH (EU Regulation No 1907/2006) compliance for polymers
    • ASTM D638 for plastic tensile properties

    Typical usage ratio

    • Utilized at 0.8%–2% by total monomer feed, adjusted based on required chain mobility, reaction time, and specific fluorination level in target polymer

    Downstream process integration

    • Introduced at the monomer copolymerization or chain-transfer step in batch or continuous polymer reactors
    • QC protocols include FTIR and NMR monitoring of fluorinated group content in pre- and post-polymerized batches

    Final product types

    • Fluorinated coating precursors for electronics and optics
    • High-durability engineering plastics for aerospace and automotive components
    • Functionalized oligomers and specialty elastomers
    Free Quote

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