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2-Fluoro-6-(Trifluoromethyl)Phenylacetonitrile

    • Product Name 2-Fluoro-6-(Trifluoromethyl)Phenylacetonitrile
    • Alias 2-Fluoro-6-(trifluoromethyl)benzyl cyanide
    • Einecs 674-065-1
    • 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
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    Specifications

    HS Code

    876936

    Product Name 2-Fluoro-6-(Trifluoromethyl)Phenylacetonitrile
    Cas Number 344086-89-9
    Molecular Formula C9H5F4N
    Molecular Weight 203.14
    Appearance White to off-white solid
    Purity Typically >97%
    Solubility Soluble in organic solvents
    Smiles N#CC1=CC=CC(F)=C1C(F)(F)F
    Inchi InChI=1S/C9H5F4N/c10-7-3-1-2-6(5-14)8(7)9(11,12)13/h1-3H,5H2
    Storage Conditions Keep in a cool, dry place, tightly closed

    As an accredited 2-Fluoro-6-(Trifluoromethyl)Phenylacetonitrile 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 25 grams of 2-Fluoro-6-(Trifluoromethyl)Phenylacetonitrile, sealed with a PTFE-lined cap and labeled for laboratory use.
    Shipping 2-Fluoro-6-(Trifluoromethyl)Phenylacetonitrile is shipped in tightly sealed containers, protected from moisture and extreme temperatures. It is packaged in accordance with local and international chemical transport regulations, including hazard labeling if required. Handle and store in a well-ventilated, cool, and dry location away from incompatible substances.
    Storage Store 2-Fluoro-6-(trifluoromethyl)phenylacetonitrile in a tightly sealed container, in a cool, dry, and well-ventilated area, away from heat, sparks, open flames, and incompatible materials such as oxidizing agents. Protect from moisture and direct sunlight. Ensure proper labeling and keep away from sources of ignition. Use suitable chemical-resistant containers and follow standard chemical storage protocols.
    Application of 2-Fluoro-6-(Trifluoromethyl)Phenylacetonitrile

    Applications of 2-Fluoro-6-(Trifluoromethyl)Phenylacetonitrile in Industrial Manufacturing

    As a direct manufacturer of 2-Fluoro-6-(Trifluoromethyl)Phenylacetonitrile, we supply this advanced intermediate to specialized chemical sectors. The following sections detail actual downstream applications, integration points, regulatory protocols, and product endpoints based on direct feedback from our global customers and partners.

    1. Agrochemical Active Ingredient Synthesis

    Major agrochemical formulators use this intermediate in synthesizing fluorinated aromatic building blocks for selective herbicides and insecticides. Our material enters the heterocyclic condensation process during the formation of triazine or pyridine derivatives, enabling targeted molecular design for regulated crop protection compounds. Formulators must balance input ratios for cost efficiency and maintain strict residual solvent controls to comply with crop-specific requirements. Reaction conditions often include controlled base-catalyzed alkylation or nucleophilic substitution, depending on the targeted 3rd or 4th generation active ingredient molecule.

    Industry compliance standards

    • FAO/WHO Specification for Pesticides
    • OECD GLP (Good Laboratory Practice) for agrochemical development
    • REACH registration dossier for European crop protection use
    • US EPA Title 40 CFR Part 158 requirements

    Typical usage ratio

    • 5–25 mol% input as stage intermediate, adjusted based on target molecule and lab-to-plant scale

    Downstream process integration

    • Reactant introduced post-nitration of base ring, prior to halogenation, in batch or closed-loop reactor

    Final product types

    • Selective triazine herbicides for maize and soybean crops
    • Pyrazole-based insecticide actives for stored grain protection
    • Pyridine-derived fungicidal agents with enhanced environmental profile
    • Custom-fluorinated intermediates for collaborative R&D projects

    2. Pharmaceutical Intermediate for CNS Drug Synthesis

    Pharmaceutical manufacturers deploy our fluorinated phenylacetonitrile in multi-step synthesis routes for active pharmaceutical ingredients (APIs) targeting central nervous system (CNS) disorders. Integration often occurs during the formation of key carbon–carbon bond linkages, such as alpha-alkylation to create phenylacetic acid derivatives. This step demands ultra-low metal residue and adherence to strict impurity thresholds, with in-process Purity (HPLC >99.5%) and enantiomeric excess validation. Processing proceeds through continuous flow or batchwise addition under nitrogen to manage potential exotherms during scale-up.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for active pharmaceutical intermediates
    • USP <823> and <857> Impurities in Pharmaceuticals
    • European Pharmacopoeia (Ph. Eur.) for chemical purity
    • FDA DMF (Drug Master File) submission requirements

    Typical usage ratio

    • 0.5–3 mol equivalents per synthetic batch, adjusted by reaction scale and targeted intermediate yield

    Downstream process integration

    • Loaded after Grignard or Friedel–Crafts acylation, at the phenyl ring functionalization step in process development

    Final product types

    • Fluorinated antiepileptic drug intermediates
    • Novel CNS-active small molecule APIs
    • Precursors for analgesic and anxiolytic compounds
    • Advanced intermediates for investigational new drug synthesis (IND-enabling studies)

    3. Electronic Chemicals for Liquid Crystal Material Production

    Leading electronic material enterprises employ our specialty intermediate during the production of high-performance liquid crystal (LC) monomers and alignment layer precursors. Integration takes place when constructing highly fluorinated aromatic cores, essential for improved dielectric anisotropy and low viscosity in LC display panels (LCDs and OLEDs). Process engineers must maintain high-purity solvent systems and fully documented batch traceability due to the critical application in optical devices. Precise input measurement and staged condensation reactions support batch reproducibility for mass-market consumer electronics.

    Industry compliance standards

    • RoHS Directive (2011/65/EU) for electronics
    • IEC 61249-2-21 for halogen content
    • JEITA guidelines for display materials
    • Internal OEM Quality Standards for electronic chemicals

    Typical usage ratio

    • 1–9 mol% as nucleophilic aromatic substitution component, optimized by final LC composition

    Downstream process integration

    • Charged post-dichloro intermediate formation, before final coupling with aliphatic side-chains in LC material synthesis

    Final product types

    • High birefringence nematic LC mixtures for TFT-LCD panels
    • Semifluorinated LC monomer blocks for OLED substrates
    • Alignment layer additives for advanced display devices
    • Electro-optic films for flexible screens and e-paper

    4. Fine Chemical Intermediate for Specialty Polymer Additives

    Producers of advanced polymers and performance additives utilize our fluorinated acetonitrile as a key element in graft copolymer synthesis and high-durability fluorinated side-chain modification. Applications demand precise molar control to achieve target molecular weight distributions, while ensuring environmental compliance regarding organofluorine residue. Our material is introduced in controlled polymerization reactions, such as controlled radical or anionic polymerization, in order to impart enhanced chemical resistance and thermal stability to engineered plastics and elastomers used in automotive, aerospace, and electronics.

    Industry compliance standards

    • ISO 9001:2015 Quality Management System for chemical production
    • REACH Annex XVII (Restriction of Substances)
    • UL Yellow Card certification for polymer safety
    • ASTM D5207 for polymer inspection

    Typical usage ratio

    • 2–12 wt% relative to base monomer feed, adjusted for mechanical and thermal property targets

    Downstream process integration

    • Metered into the copolymerization reactor following main chain propagation, prior to end-capping or compounding

    Final product types

    • Fluorinated impact modifiers for high-heat plastics
    • Specialty elastomer additives for sealing gaskets
    • Surface treatment resins for wire coatings
    • Antistatic agents for specialty films
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