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HS Code |
838476 |
| Chemical Name | 2,3,4-Trifluorobenzamide |
| Molecular Formula | C7H4F3NO |
| Molecular Weight | 175.11 g/mol |
| Cas Number | 1736-74-9 |
| Appearance | White to off-white solid |
| Melting Point | 115-118 °C |
| Boiling Point | Unknown |
| Density | 1.48 g/cm3 (estimated) |
| Solubility In Water | Slightly soluble |
| Purity | Typically ≥98% |
| Smiles | C1=CC(=C(C(=C1F)F)F)C(=O)N |
| Inchi | InChI=1S/C7H4F3NO/c8-4-2-1-3(7(11)12)5(9)6(4)10/h1-2H,(H2,11,12) |
| Synonyms | Benzamide, 2,3,4-trifluoro- |
| Storage Conditions | Store at room temperature, in a dry place |
As an accredited 2,3,4-Trifluorobenzamide factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | A 25g amber glass bottle with a secure screw cap, labeled "2,3,4-Trifluorobenzamide," including hazard and handling information. |
| Shipping | 2,3,4-Trifluorobenzamide is typically shipped in tightly sealed containers to prevent contamination and moisture exposure. It should be transported in compliance with relevant chemical safety regulations, including proper labeling and documentation. The package must be handled with care, avoiding extreme temperatures and physical damage during transit to ensure safety and product integrity. |
| Storage | 2,3,4-Trifluorobenzamide should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from incompatible substances such as strong oxidizers. Protect from moisture and direct sunlight. Store at room temperature and keep container tightly closed when not in use to prevent contamination and degradation. Follow all relevant safety guidelines for handling chemicals. |
Applications of 2,3,4-Trifluorobenzamide in Industrial ManufacturingAs the direct producer of 2,3,4-Trifluorobenzamide, we support its use in multiple specialized chemical and pharmaceutical sectors. Below, we outline specific downstream industries where manufacturing partners employ this intermediate, with focused details on industrial standards, precise formulation levels, integration points, and real-world finished goods. 1. Active Pharmaceutical Ingredient (API) Intermediate for Antipsychotic Synthesis2,3,4-Trifluorobenzamide serves as a core structural intermediate in the synthesis of several tricyclic antipsychotic APIs, especially within the development of selective serotonin and dopamine modulators. Pharmaceutical manufacturers incorporate this building block during multi-step organic synthesis to introduce specific trifluorophenyl moieties essential for pharmacological activity, achieving both process compliance and consistent purity profiles across commercial API batches. Industry compliance standards
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2. Crop Protection Compound Manufacturing (Herbicides & Fungicides)Agrochemical formulators utilize 2,3,4-Trifluorobenzamide to construct advanced active ingredients with selective foliage activity. Its introduction permits the targeted design of aromatic amide scaffolds that display persistent bioactivity and metabolic stability, commonly in the development of next-generation benzamide-based herbicides and fungicide agents for field crops. Downstream users rigorously monitor structural purity to adhere to environmental and safety statutes. Industry compliance standards
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3. Specialty Monomer in Advanced Polymer MaterialsResin and polymer compounders select 2,3,4-Trifluorobenzamide as a specialty monomeric component to impart hydrophobicity, chemical resistance, and specific dielectric properties in engineered polymers. This building block introduces trifluoro-functional groups into polyamide or polyarylamide chains, supporting downstream customization for separator films, protective coatings, and high-frequency electronics substrates. Quality controls focus on conversion rates and end-use environmental exposure. Industry compliance standards
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4. Fine Chemical Intermediate for Aryl Amide SynthesisCustom synthesis laboratories and fine chemical producers employ 2,3,4-Trifluorobenzamide as a key intermediate in the preparation of aryl amide derivatives. It provides tight control over the introduction of trifluorinated aromatic motifs when crafting high-purity intermediates for dyes, fluorescence markers, and molecular sensors. Fine chemicals QA teams enforce analytic characterization for each batch, guaranteeing suitability for further functionalization. Industry compliance standards
Typical usage ratio
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