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HS Code |
656350 |
| Product Name | Sodium 3-Trifluoromethylbenzoate |
| Cas Number | 402-40-0 |
| Molecular Formula | C8H4F3NaO2 |
| Molecular Weight | 212.10 |
| Appearance | White to off-white powder |
| Solubility In Water | Soluble |
| Ph | Neutral to slightly basic (in aqueous solution) |
| Storage Temperature | Room temperature |
| Synonyms | Sodium m-(Trifluoromethyl)benzoate |
| Smiles | C1=CC(=CC(=C1)C(=O)[O-])C(F)(F)F.[Na+] |
| Inchi | InChI=1S/C8H5F3O2.Na/c9-8(10,11)6-3-1-2-5(4-6)7(12)13;/h1-4H,(H,12,13);/q;+1/p-1 |
| Ec Number | 606-372-1 |
As an accredited Sodium 3-Trifluoromethylbenzoate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 100g of Sodium 3-Trifluoromethylbenzoate is supplied in a sealed amber glass bottle with a tamper-evident cap and hazard labeling. |
| Shipping | Sodium 3-Trifluoromethylbenzoate is shipped in tightly sealed containers, protected from moisture and incompatible substances. The packaging complies with relevant chemical transport regulations. The product is labeled for laboratory use, with safety information provided. Standard shipping is via ground or air freight, depending on destination and urgency, ensuring product stability during transit. |
| Storage | Store **Sodium 3-Trifluoromethylbenzoate** in a tightly sealed container, kept in a cool, dry, and well-ventilated area. Protect from moisture, direct sunlight, and incompatible materials such as acids and strong oxidizers. Ensure storage is away from heat sources. Clearly label the container and keep it in accordance with local regulations and laboratory safety standards. |
Applications of Sodium 3-Trifluoromethylbenzoate in Industrial ManufacturingSodium 3-Trifluoromethylbenzoate functions as a critical intermediate in the development and scalable synthesis of various high-value chemicals across pharmaceutical, agrochemical, polymer, and specialty chemicals sectors. Its distinctive trifluoromethyl group contributes unique properties that downstream manufacturers require for innovative active ingredient development, structural modification, or end product performance enhancements. As the original manufacturer, we supply this building block to global partners who demand reliability, traceability, and technical transparency at every stage of their application chain. 1. Active Pharmaceutical Ingredient (API) Intermediate SynthesisDrug manufacturers utilize this compound during the construction of specialized aromatic motifs integral to the development of fluorine-containing pharmaceuticals, including central nervous system agents and anti-inflammatory drugs. It often serves in key steps such as Suzuki or Buchwald coupling, enabling downstream substitution and final API formation while maintaining strict regulatory compliance with major pharmacopoeias. Industry compliance standards
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2. Agrochemical Herbicide IntermediateMajor crop protection producers introduce this raw material as a starting block in synthesizing trifluoromethyl-substituted benzoic acid derivatives widely used in post-emergent herbicides. Fluorination enhances both activity and metabolic stability, supporting formulation of selective weed control agents. Quality teams follow the most recent environmental and industry regulations when incorporating upstream intermediates. Industry compliance standards
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3. Advanced Polymer Monomer ManufacturingProducers of fluorinated specialty polymers and high-performance resins leverage the chemical’s electron-withdrawing capabilities to modify aromatic ring systems, imparting distinct chemical resistance and surface properties for demanding technical applications. End users benefit from low dielectric constant, improved weatherability, and tailored hydrophobicity essential in electronics and architectural coatings. Industry compliance standards
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4. Specialty Fine Chemical SynthesisManufacturers in the fine chemicals sector introduce sodium 3-trifluoromethylbenzoate during the multi-step synthesis of custom aromatic compounds with unique reactivity profiles. Its trifluoromethyl group remains stable under a range of electrophilic and nucleophilic conditions, supporting the design of advanced dyes, photoactive materials, or functional additives for industrial R&D sectors requiring validated traceability and batch-to-batch consistency. Industry compliance standards
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