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HS Code |
782068 |
| Cas Number | 14309-87-6 |
| Molecular Formula | C9H7F3O |
| Molecular Weight | 188.15 |
| Iupac Name | 1-[3-(trifluoromethyl)phenyl]ethan-1-one |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 92-94 °C at 17 mmHg |
| Melting Point | -10 °C |
| Density | 1.217 g/cm3 at 25 °C |
| Refractive Index | 1.4740-1.4760 |
| Solubility | Insoluble in water, soluble in organic solvents |
| Purity | Typically >98% |
| Smiles | CC(=O)C1=CC(=CC=C1)C(F)(F)F |
As an accredited 3'-(Trifluoromethyl)Acetophenone factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle with screw cap containing 25 grams of 3'-(Trifluoromethyl)Acetophenone, labeled with chemical name, hazard symbols, and batch number. |
| Shipping | 3'-(Trifluoromethyl)Acetophenone is shipped in sealed, chemical-resistant containers compliant with international safety regulations. Packaging ensures protection from moisture and light, with clear hazard labeling. Transport follows guidelines for flammable organic compounds. Temperature is controlled as required, and all documentation, including Safety Data Sheets (SDS), accompanies the shipment for safe handling and receipt. |
| Storage | Store **3'-(Trifluoromethyl)acetophenone** 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. Keep out of direct sunlight and moisture. Use appropriate chemical-resistant gloves and safety goggles when handling. Ensure proper labeling and follow all local regulations for storage of organic chemicals. |
Applications of 3'-(Trifluoromethyl)Acetophenone in Industrial ManufacturingAs the direct manufacturer of 3'-(Trifluoromethyl)Acetophenone, we serve leading industrial partners across multiple sectors where stringent material sourcing and precision chemical integration are imperative. Below, we present key application areas, each demonstrating specialized requirements in regulatory compliance, formulation, production methodology, and downstream product development. 1. Pharmaceutical Intermediate for Active Pharmaceutical Ingredient (API) SynthesisPharmaceutical companies source this material as a building block for synthesizing fluorinated APIs, particularly within anti-inflammatory, antiviral, and central nervous system (CNS) therapeutic classes. Its incorporation typically takes place early in multi-step organic synthesis, where electronic and lipophilic modification via the trifluoromethyl group directly impacts the pharmacological profile and metabolic stability of the target compound. Manufacturing sites must validate trace impurities and thoroughly document batch production processes to meet global regulatory demands. Industry compliance standards
Typical usage ratio
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2. Agrochemical Intermediate for Herbicide and Pesticide SynthesisAgrochemical formulators utilize this intermediate chiefly for the preparation of advanced fluorinated herbicides and fungicides, which require precise fluorine placement to achieve target bioactivity and environmental persistence. During large-scale synthesis, technicians add it during the acylation or aromatic substitution stage, often requiring on-site purification and waste management controls to comply with environmental discharge limits and product registration guidelines. Industry compliance standards
Typical usage ratio
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3. Specialty Chemical Synthesis for Liquid Crystal MaterialsManufacturers of advanced display technologies incorporate this raw material for the design of liquid crystal (LC) compounds used in TFT-LCD and OLED displays. The introduction of the trifluoromethyl aromatic segment imparts distinct dielectric and phase-transition characteristics vital to screen performance and energy consumption. Production teams control addition during the primary condensation or aromatic substitution phase within restricted-access cleanrooms. Industry compliance standards
Typical usage ratio
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4. Fine Fragrance and Aromatic Chemicals DevelopmentFragrance compounders include this acetophenone derivative during top-note and heart-note molecule synthesis, leveraging the unique sensory profile introduced by the trifluoromethyl group. Processing typically happens within regulated fragrance laboratories, focusing on purity, stability, and compliance with international fragrance ingredient safety standards, followed by robust quality control during blending for end-user products. Industry compliance standards
Typical usage ratio
Downstream process integration
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