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2,3,4,5-Tetrafluorobenzonitrile

    • Product Name 2,3,4,5-Tetrafluorobenzonitrile
    • Alias 2,3,4,5-Tetrafluorobenzene Carbonitrile
    • Einecs 809-820-5
    • 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

    104684

    Chemical Name 2,3,4,5-Tetrafluorobenzonitrile
    Cas Number 2247-26-1
    Molecular Formula C7HF4N
    Molecular Weight 175.08
    Appearance White to pale yellow solid
    Melting Point 53-56°C
    Boiling Point 175-177°C at 30 mmHg
    Density 1.540 g/cm3
    Solubility Slightly soluble in water, soluble in organic solvents
    Smiles C1=C(C(=C(C(=C1F)F)C#N)F)F
    Pubchem Cid 139149

    As an accredited 2,3,4,5-Tetrafluorobenzonitrile factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing A 25-gram amber glass bottle with a secure screw cap, labeled "2,3,4,5-Tetrafluorobenzonitrile, CAS 57311-80-7, for laboratory use."
    Shipping 2,3,4,5-Tetrafluorobenzonitrile should be shipped in tightly sealed containers, protected from moisture and incompatible substances. Transport in accordance with applicable regulations for hazardous chemicals. Store in a cool, well-ventilated area. Ensure proper labeling and use secondary containment to prevent leaks during transit. Handle with appropriate personal protective equipment.
    Storage 2,3,4,5-Tetrafluorobenzonitrile should be stored in a tightly closed container, in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible materials such as strong oxidizers. Protect from moisture and direct sunlight. Handle under inert atmosphere if possible, and use appropriate personal protective equipment to avoid contact and inhalation. Store according to local regulations.
    Application of 2,3,4,5-Tetrafluorobenzonitrile

    Applications of 2,3,4,5-Tetrafluorobenzonitrile in Industrial Manufacturing

    2,3,4,5-Tetrafluorobenzonitrile serves as a high-value intermediate in multiple downstream chemical production sectors. Drawing on consistent batch quality and scalable production control, our material supports demanding processing environments for end users who require chemoselectivity and high purity. Below, we have detailed its primary applications across industrial fields that rely on stringent compliance, precise formulation design, and controlled process integration at scale.

    1. Agrochemical Intermediate Synthesis

    Major agrochemical producers utilize this raw material as a building block in the manufacture of active ingredients for advanced herbicides and selective insecticides. Its electron-deficient aromatic ring facilitates nucleophilic aromatic substitution, supporting the synthesis of fluorinated aromatic pesticides with increased metabolic stability. Our manufacturing processes deliver tight impurity profiles suitable for crop protection formulation requirements.

    Industry compliance standards

    • FAO/WHO Specification for Pesticides (JMPS)
    • ISO 9001:2015 in chemical intermediate production
    • REACH Regulation (EC) No 1907/2006 compliance for substance registration
    • APVMA, EPA, and relevant national agrochemical regulations

    Typical usage ratio

    • 10–30% by mole in precursor coupling reactions, adjusted based on substitution pathway and catalyst system

    Downstream process integration

    • Introduced during aromatic substitution or amidoxime coupling steps for fluorinated ring construction; batch loading occurs after pre-purification of core intermediates

    Final product types

    • Fluorinated herbicides
    • Systemic and contact insecticides with increased soil stability
    • Synthesis intermediates for fungicidal actives

    2. Pharmaceutical Building Block

    Innovators and generic manufacturers employ this compound in the synthesis of specialty fluorinated aromatic scaffolds that require precise regioselectivity. Its cyano group activates adjacent carbon atoms, streamlining subsequent functionalization for drug candidate development, especially in non-steroidal anti-inflammatory and antineoplastic agent manufacturing.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • US FDA cGMP 21 CFR Part 211
    • European Pharmacopoeia (Ph. Eur.) for impurity control in intermediates
    • USP General Chapters where relevant to APIs

    Typical usage ratio

    • 15–45% stoichiometric addition, tailored to route of synthesis and multistep yield optimization

    Downstream process integration

    • Added post-chlorination or pre-condensation, enabling downstream functional group transformations prior to API crystallization; batch and flow chemistry compatible

    Final product types

    • Non-steroidal anti-inflammatory drug (NSAID) intermediates
    • Fluorinated kinase inhibitor scaffolds
    • Precursor molecules for CNS-active pharmaceuticals

    3. Specialty Polymer Monomers

    Producers of high-performance engineering plastics and fluoropolymers select this raw material as a reactive monomer for synthesizing polymers that demand strong chemical resistance and low dielectric constants. Its multiple fluorine substituents impart hydrophobicity and reduced surface energy, critical for processability and end-use durability in electronics and filtration applications.

    Industry compliance standards

    • ISO 14001 for polymer manufacturing environmental controls
    • RoHS Directive (2011/65/EU) for electronics-related materials
    • REACH Authorization for specialty monomers
    • UL 94 (for polymer flame retardancy assessment)

    Typical usage ratio

    • 2–8% of total monomer mass; ratio varies with copolymerization system and targeted polymer architecture

    Downstream process integration

    • Integrated into aromatic copolymerizations or polycondensation reactions, typically as a minor component to modify matrix properties; added after pre-polymer preparation for precision properties

    Final product types

    • Fluoropolymer coatings for electronics and wire insulation
    • Heat-resistant filter materials
    • Low-surface-energy membranes for industrial separation

    4. Liquid Crystal Material Synthesis

    Manufacturers of advanced display materials incorporate this fluorinated benzonitrile in synthesizing key intermediates for nematic and smectic liquid crystal compounds. The specific fluorine substitution pattern influences dipole alignment and phase transition temperatures, optimizing end-use performance in high-resolution panel displays for the electronics sector.

    Industry compliance standards

    • ISO 9001:2015 for electronic material synthesis
    • RoHS 3 (EU 2015/863) substance restrictions for display chemicals
    • IEC 61249-2-21 for halogen-free content management
    • REACH compliance for electronic chemical intermediates

    Typical usage ratio

    • 1–5% of total molar composition within liquid crystal intermediate production, adjustable based on target viscosity and electro-optical properties

    Downstream process integration

    • Condensed with alkyl or cyclic substituents via etherification or Suzuki coupling after purification to electronic grade, supporting strict panel QC standards

    Final product types

    • Nematic and smectic liquid crystal mixtures for TFT and IPS-LCD displays
    • Compounds for OLED and advanced monitor applications
    • Electronic-grade intermediates for display module assembly
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