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3,5-Di(Trifluoromethyl)Benzamide

    • Product Name 3,5-Di(Trifluoromethyl)Benzamide
    • Alias 3,5-Bis(trifluoromethyl)benzamide
    • Einecs 228-340-4
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry sales7@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    475776

    Product Name 3,5-Di(Trifluoromethyl)Benzamide
    Cas Number 328-99-6
    Molecular Formula C9H5F6NO
    Molecular Weight 261.13
    Appearance White to off-white crystalline powder
    Melting Point 152-156 °C
    Purity Typically ≥98%
    Density 1.61 g/cm³ (estimated)
    Solubility Slightly soluble in water, soluble in organic solvents such as DMSO and DMF
    Smiles C1=CC(=C(C=C1C(F)(F)F)C(=O)N)C(F)(F)F
    Inchi InChI=1S/C9H5F6NO/c10-8(11,12)5-1-6(9(13,14)15)3-4(2-5)7(16)17/h1-3H,(H2,16,17)
    Storage Condition Store at 2-8°C, tightly closed
    Ec Number 206-410-6

    As an accredited 3,5-Di(Trifluoromethyl)Benzamide factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle containing 10 grams of 3,5-Di(Trifluoromethyl)Benzamide, labeled with product details, safety symbols, and hazard information.
    Shipping 3,5-Di(Trifluoromethyl)Benzamide is shipped in tightly sealed containers, protected from moisture and light. It is packed according to standard chemical safety protocols, with clear labeling and accompanying documentation. Transport is conducted via ground or air freight in compliance with local and international hazardous materials regulations, ensuring safe and secure delivery.
    Storage Store 3,5-Di(trifluoromethyl)benzamide in a tightly sealed container, in a cool, dry, and well-ventilated area. Keep away from sources of ignition, strong acids, bases, and oxidizing agents. Avoid exposure to moisture and direct sunlight. Label storage clearly and follow appropriate chemical hygiene and safety protocols. Ensure access is restricted to trained personnel and use personal protective equipment when handling.
    Application of 3,5-Di(Trifluoromethyl)Benzamide

    Applications of 3,5-Di(Trifluoromethyl)Benzamide in Industrial Manufacturing

    3,5-Di(Trifluoromethyl)Benzamide finds use in advanced chemical synthesis and specialty manufacturing across several focused industrial sectors. We engage directly with large-volume consumers in pharmaceuticals, agrochemicals, electronics, polymer additives, and advanced coatings, supporting strict process controls, high purity demands, and audited supply chains. Here we present principal application areas, each with specific regulatory, production, and finished product data relevant for industrial purchasing and technical teams.

    1. Pharmaceutical Intermediate Synthesis

    Major pharmaceutical manufacturers use this compound as a key intermediate during the multi-step synthesis of active pharmaceutical ingredients (APIs), especially in fluorinated small-molecule drug pipelines. It integrates early in the process to introduce trifluoromethyl groups, which impact bioavailability and metabolic stability. Process chemists select it for custom molecule scaffolding, particularly for third- and fourth-generation therapeutic programs where repeated structure-activity-relationship modifications demand high-yield and consistent analytical profiles batch-to-batch.

    Industry compliance standards

    • ICH Q7 (Good Manufacturing Practice Guide for Active Pharmaceutical Ingredients)
    • USP/NF Monographs (where applicable for intermediates)
    • 21 CFR Part 211 (U.S. FDA GMP for Finished Pharmaceuticals)
    • EDQM CEP Procedures (for API route of synthesis registration)

    Typical usage ratio

    • Intermediate-to-final API molar ratios range from 1:1 to 1:3, adjusted for target molecular weight and step yield requirements
    • Batch input rates determined by desired synthesis scale, typically 0.5–1.2 kg per 1 kg target API

    Downstream process integration

    • Material charged in condensation or acylation reaction steps, often during early-stage or mid-stage step-up synthesis
    • Purification follows via crystallization or flash chromatography; rigorous in-process QC for residuals

    Final product types

    • Novel fluorinated APIs for anti-inflammatory, antiviral, and oncology applications
    • Custom intermediates used by contract manufacturing organizations (CMOs)

    2. Agrochemical Active Ingredient Development

    Formulators in the crop protection sector incorporate this compound as a building block in the synthesis of advanced herbicides and fungicides. The compound’s electronic properties enable precise modulation of agrochemical physicochemical profiles, such as lipid solubility and photostability. It is introduced during selective aromatic substitution to rationalize the balance of environmental degradability and field persistence, meeting major regulatory requirements for residue and non-target organism impact.

    Industry compliance standards

    • OECD Guidelines for the Testing of Chemicals (Synthesis and Characterization)
    • FAO/WHO Pesticide Specifications (JMPS standards)
    • REACH registration dossier (for use in EU-based development)
    • ISO 9001:2015 certified quality management systems

    Typical usage ratio

    • Used at 0.7–2.0 equivalents in aromatic substitution or coupling protocols, relative to base aryl substrate
    • Batchwise loading adjusted based on target yield; process engineers optimize charge rates for downstream scalability

    Downstream process integration

    • Material dosed in pilot-scale and commercial-scale batch synthesis lines, typically following initial aromatic nitration/reduction
    • Downstream purification via phase separation and solid–liquid extraction methods

    Final product types

    • Selective post-emergence herbicides with enhanced rainfastness
    • Triazole-based fungicide actives
    • Seed treatment active ingredients

    3. Advanced Electronics Sector—Liquid Crystal Display (LCD) Materials

    Manufacturers in the electronics sector employ the compound as an intermediate in the synthesis of high-performance liquid crystal materials. With strong electron-withdrawing capacity and rigid aromatic structure, the compound enhances dielectric properties and thermal stability needed for next-generation display production. Formulators use fine-tuned blends that improve viewing angle and color depth while upholding high manufacturing reproducibility required by panel OEMs.

    Industry compliance standards

    • IEC 61249-2-21: Halogen-free materials requirements
    • RoHS Directive 2011/65/EU (Restriction of Hazardous Substances in Electronics)
    • JIS C 6109-2-1: Japanese Industrial Standard for materials used in display applications
    • ISO/TS 16949: Quality management systems for automotive electronics

    Typical usage ratio

    • Used at 0.3–0.8 moles per mole of base anisotropic material, determined by target phase transition temperature and viscosity
    • Solution blending ratios verified by pre-production simulation data

    Downstream process integration

    • Added during stepwise condensation or direct fluorination reactions on custom LCD precursor lines
    • Purity and trace metal residues monitored by LC–MS ahead of cell assembly

    Final product types

    • High-resolution TFT LCD panels
    • Specialty liquid crystal mixtures for automotive and industrial instrumentation

    4. Polymer Additive for Fluorinated Resin Performance

    Specialty polymer manufacturers utilize the compound as an additive during the production of fluorinated engineering resins, such as polyvinylidene fluoride (PVDF) and fluorinated polyimides. Its incorporation modifies chain architecture to improve dielectric constant, chemical inertness, and processability for use in highly demanding environments, such as semiconductor device insulation, cable jacketing, and specialty filtration membranes. Careful raw material flow control ensures stable copolymerization and reduced side reactions.

    Industry compliance standards

    • ASTM D5630 (Standard Test Method for ash content in fluoropolymer resins)
    • UL 94 (Flammability testing for plastic materials)
    • ISO 14001: Environmental management in plastics manufacturing
    • TSCA Inventory (U.S. EPA Chemical Substance Compliance)

    Typical usage ratio

    • Normally incorporated at 0.5–3.0 wt% relative to total monomer feed, depending on final dielectric specification and mechanical targets
    • Optimized for chain length distribution and reactivity ratio studies in pilot compounding lines

    Downstream process integration

    • Dosed in continuous or batch copolymerization lines, with inline feed verification
    • Residuals sampled post-extrusion to confirm target distribution profiles

    Final product types

    • High-purity PVDF films for lithium-ion battery separators
    • Fluoropolyimide coatings for flexible printed circuits
    • Microporous filtration membranes for medical and industrial use

    5. Surface Modification Agent in High-Performance Coatings

    Coating formulators use the compound for functional surface modification in high-resistance paints and industrial finishes, focusing on sectors that demand extreme chemical and thermal durability—such as aerospace and chemical processing equipment manufacturing. The molecule’s dual trifluoromethyl functionality delivers controlled hydrophobicity and low surface energy, offering long-term stability against aggressive solvents, acids, and UV radiation after application.

    Industry compliance standards

    • ISO 12944-6 (Corrosion protection of steel structures by protective paint systems)
    • ASTM D3359 (Adhesion testing for coating films)
    • EN 13523-10 (Resistance to solvents and chemicals for coil coatings)
    • REACH Annex XVII SVHC (regulation of persistent, bioaccumulative, and toxic substances)

    Typical usage ratio

    • Blended into resin phase at 0.8–2.5 wt% for specialty topcoats
    • Optimized by end-user labs to meet specific hydrophobicity (contact angle >115°) and mechanical abrasion ratings

    Downstream process integration

    • Dispersed into pre-polymer mix prior to pigment addition on high-shear mixing lines
    • Applied via spray or roll-coat, cured in controlled environments for crosslinking

    Final product types

    • Aircraft exterior coatings resistant to hydraulic fluids and jet fuel
    • Chemical storage tank linings
    • Specialty exterior paints for off-shore and marine equipment
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