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Sodium 3-Trifluoromethylbenzoate

    • Product Name Sodium 3-Trifluoromethylbenzoate
    • Alias Sodium 3-(trifluoromethyl)benzoate
    • Einecs 251-537-6
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    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 & Storage
    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.
    Application of Sodium 3-Trifluoromethylbenzoate

    Applications of Sodium 3-Trifluoromethylbenzoate in Industrial Manufacturing

    Sodium 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 Synthesis

    Drug 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

    • ICH Q7 GMP for Active Pharmaceutical Ingredients
    • USP/NF and Ph. Eur. for excipient and intermediate purity
    • FDA 21 CFR Part 210/211 procedural controls
    • EDQM CEP for traceability

    Typical usage ratio

    • 0.5–3.5 molar equivalents, depending on the desired substitution pattern and reaction pathway; process chemists adjust based on target molecule and stoichiometry in multistep synthesis

    Downstream process integration

    • Coupling reactions with boronic acids or halides in palladium-catalyzed systems, typically entering after initial core scaffold assembly and pre-purification workups

    Final product types

    • Fluorinated drug candidates
    • Active pharmaceutical ingredients for CNS therapies
    • Orally administered anti-inflammatory drugs
    • Advanced pharmaceutical intermediates for contract manufacturing

    2. Agrochemical Herbicide Intermediate

    Major 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

    • FAO/WHO specifications for technical grade chemicals
    • ISO 9001:2015 for quality management and traceability
    • EPA 40 CFR for chemical substances in pesticides
    • REACH Annex VII (EU) for registration and pre-manufacture notification

    Typical usage ratio

    • 10–30% by mole of total aromatic intermediates in the synthesis route, tuned for each herbicide formulation according to target selectivity and potency profile

    Downstream process integration

    • Nucleophilic aromatic substitution, followed by free acid hydrolysis and re-esterification to produce target actives; typically charged into the reactor during the early aromatic derivatization phase

    Final product types

    • Selective post-emergent herbicide actives with enhanced rainfastness
    • Trifluoromethyl-benzenoid herbicide intermediates
    • Commercial crop protection agents for cereals and broadleaf weeds

    3. Advanced Polymer Monomer Manufacturing

    Producers 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

    • ISO 14001 for environmental management in fluoropolymer synthesis
    • RoHS Directive 2011/65/EU for hazardous substance restriction
    • UL 94 for flame retardancy of finished polymers
    • ASTM D638 for mechanical quality control of polymer products

    Typical usage ratio

    • 5–15% relative to total aromatic feedstock blend; exact loading determined by targeted surface energy and physical property profile in the resulting copolymer matrix

    Downstream process integration

    • Monomer functionalization via esterification or amidation, typically followed by melt or solution-phase (co)polymerization with styrenic, acrylate, or ether comonomers

    Final product types

    • Fluorinated thermoset and thermoplastic resins
    • High-performance coatings for electronics and aerospace
    • Advanced membrane materials
    • Weather- and chemical-resistant architectural polymers

    4. Specialty Fine Chemical Synthesis

    Manufacturers 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

    • ISO 9001 for documented quality and processing controls
    • GHS/CLP for hazard classification and labeling conformity
    • Internal client-specific raw material and impurity specifications
    • REACH (EC) No. 1907/2006 for substance registration where applicable

    Typical usage ratio

    • 1–10% by weight in target aromatic coupling reactions, adjusted according to substitution pattern and end-use reactivity consideration

    Downstream process integration

    • Charged as a coupling partner or aromatic base for custom synthesis projects following core compound activation or halogenation steps

    Final product types

    • Non-ionic and ionic dyes for optical applications
    • Photoactive industrial intermediates
    • Functional additives for polymers and lubricants
    • Custom fine chemicals for pharmaceutical and electronic R&D markets
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