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HS Code |
616613 |
| Productname | Methyl 2-Trifluoromethylbenzoylacetate |
| Casnumber | 699-43-2 |
| Molecularformula | C11H9F3O3 |
| Molecularweight | 246.18 |
| Purity | Typically >98% |
| Appearance | Colorless to pale yellow liquid |
| Density | 1.32 g/cm3 |
| Boilingpoint | 114-116°C at 20 mmHg |
| Solubility | Soluble in organic solvents such as ether and chloroform |
| Smiles | COC(=O)CC(=O)c1ccccc1C(F)(F)F |
| Inchi | InChI=1S/C11H9F3O3/c1-17-10(16)6-9(15)7-4-2-3-5-8(7)11(12,13)14/h2-5H,6H2,1H3 |
| Refractiveindex | n20/D 1.491 |
| Storagetemperature | 2-8°C |
As an accredited Methyl 2-Trifluoromethylbenzoylacetate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle, sealed cap, 25 grams, white printed label displaying chemical name, CAS number, hazard pictogram, and supplier logo. |
| Shipping | Methyl 2-Trifluoromethylbenzoylacetate is shipped in tightly sealed, chemical-resistant containers to prevent leaks and contamination. Packages are labeled according to hazardous materials regulations and stored away from incompatible substances. During transit, the chemical is kept at controlled temperatures and protected from moisture and sunlight to ensure stability and safety. |
| Storage | Methyl 2-Trifluoromethylbenzoylacetate should be stored in a tightly closed container in a cool, dry, and well-ventilated area away from sources of heat, ignition, and incompatible substances such as strong oxidizers. Protect it from moisture and direct sunlight. Ensure proper labeling, and use secondary containment to prevent leaks or spills. Store in compliance with local regulations and chemical safety guidelines. |
Applications of Methyl 2-Trifluoromethylbenzoylacetate in Industrial ManufacturingAs the original manufacturer of Methyl 2-Trifluoromethylbenzoylacetate, we supply this high-purity intermediate directly to core sectors where demand for specialty aromatic compounds and fine chemicals is rapidly growing. Its molecular structure enables use in multiple downstream industries, each with specific technical, compliance, and processing requirements. 1. Pharmaceutical Active Ingredient SynthesisOur material is widely employed by API manufacturers as a crucial intermediate in the synthesis of advanced pharmaceutical compounds, including selective kinase inhibitors and central nervous system agents. The electron-withdrawing trifluoromethyl group facilitates regioselective condensation and alkylation, ensuring consistent batch-to-batch reactivity in multi-step synthesis. Our product consistently meets strict impurity profiles demanded for regulated drug substance manufacture. Downstream formulators integrate it during core structure assembly, prior to final salt formation, ensuring maintainable critical process parameters for regulatory submission. Industry compliance standards
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2. Agrochemical Intermediate ProductionAgrochemical formulators utilize Methyl 2-Trifluoromethylbenzoylacetate in the design and scale-up of advanced herbicides and fungicides featuring trifluoromethylated phenyl cores. Its clean reaction profile and high assay deliver robust yields in Knoevenagel condensation, allowing agrochemical manufacturers to maintain consistency in pilot and full-scale production. We tailor our specification for the synthesis of actives subjected to global residue, toxicity, and environmental persistence assessments. Industry compliance standards
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3. Specialty Dye and Pigment ManufacturingDye manufacturers select this compound for introducing stable trifluoromethyl groups into high-performance organic pigments and dyes targeting industrial coatings, plastics, and electronic displays. Engineered for high colorfastness and weather-resistance, our material ensures superior chemical compatibility in condensation processes operated at elevated temperatures. We guarantee tight control of aromatic impurities for consistent optical properties in downstream product lines. Industry compliance standards
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4. Fine Chemical Building Block SupplyCustom fine chemical producers incorporate Methyl 2-Trifluoromethylbenzoylacetate as a structural unit in advanced synthesis schemes for specialty chemicals and research standards. The compound’s reactivity profile enables selective transformations such as oxime, hydrazone, or enolate formation under controlled laboratory and plant conditions. Designed for professional formulation labs, we keep ultra-low water and residual solvent content, ensuring reliable downstream conversion yields for proprietary molecules. Industry compliance standards
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