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2-Fluoro-3-(Trifluoromethyl)Phenylacetonitrile

    • Product Name 2-Fluoro-3-(Trifluoromethyl)Phenylacetonitrile
    • Alias 2-fluoro-3-(trifluoromethyl)benzyl cyanide
    • Einecs 632-236-5
    • 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
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    Specifications

    HS Code

    456791

    Productname 2-Fluoro-3-(Trifluoromethyl)Phenylacetonitrile
    Casnumber 1052717-85-3
    Molecularformula C9H5F4N
    Molecularweight 203.14
    Appearance Colorless to light yellow liquid
    Purity Typically ≥98%
    Synonyms α-Cyano-2-fluoro-3-(trifluoromethyl)toluene
    Smiles N#CCc1cccc(F)c1C(F)(F)F
    Inchi InChI=1S/C9H5F4N/c10-8-3-2-6(5-14)7(4-8)9(11,12)13/h2-4H,5H2
    Storagetemperature 2-8°C

    As an accredited 2-Fluoro-3-(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, 25 grams, white screw cap, tamper-evident seal, chemical label with hazard warnings, batch number, and CAS info.
    Shipping 2-Fluoro-3-(trifluoromethyl)phenylacetonitrile is shipped in tightly sealed containers, protected from moisture and light. It is transported as a chemical substance in accordance with relevant regulations, typically via ground or air freight. Appropriate hazard labeling and documentation accompany the shipment to ensure safe handling and regulatory compliance.
    Storage Store 2-Fluoro-3-(trifluoromethyl)phenylacetonitrile in a tightly sealed container, away from moisture and incompatible substances such as strong acids and bases. Keep the container in a cool, dry, and well-ventilated area, preferably in a dedicated flammable chemical storage cabinet. Protect from direct sunlight, heat, and ignition sources. Always label containers appropriately and follow standard chemical safety protocols.
    Application of 2-Fluoro-3-(Trifluoromethyl)Phenylacetonitrile

    Applications of 2-Fluoro-3-(Trifluoromethyl)Phenylacetonitrile in Industrial Manufacturing

    2-Fluoro-3-(Trifluoromethyl)Phenylacetonitrile serves as a specialized intermediate in several industrial manufacturing sectors where stringent quality and process controls are critical. With advanced synthesis compatibility and precise functional group support, this material plays an integral role in active pharmaceutical ingredient development, crop protection manufacturing, advanced materials innovation, and fine chemical synthesis. The following key application segments reflect established industrial routes and illustrate how leading producers achieve safe integration under recognized global standards.

    1. Pharmaceutical API Synthesis

    This intermediate is utilized in the multi-step synthesis of active pharmaceutical ingredients, contributing specific fluorinated motifs which enhance the target compound’s metabolic stability and bioavailability. Pharmaceutical manufacturers introduce it at controlled stages to enable fluorine incorporation within regulated process environments, ensuring that each batch supports necessary documentation and traceability for regulated markets.

    Industry compliance standards

    • ICH Q7 GMP Guidelines for API Manufacturing
    • US FDA 21 CFR Part 211 (cGMP)
    • European Pharmacopeia Monographs
    • Chinese Pharmacopoeia Standards

    Typical usage ratio

    • Applied at precursor stage, typically 0.8–5 mol% relative to final API yield, adjusted based on reaction scale and downstream conversion efficiency

    Downstream process integration

    • Charged during intermediate step following halide activation and prior to heterocycle formation, under temperature-controlled, closed reactor systems involving base-catalyzed reactions

    Final product types

    • Fluorinated quinolones
    • Pyridine-based anti-infectives
    • Specialty cardiovascular agents

    2. Agrochemical Synthesis (Herbicide & Fungicide Intermediates)

    In crop protection manufacturing, the compound supports the introduction of fluorinated aryl groups into advanced herbicide and fungicide ingredients. Producers rely on its dimensional purity and reactive profile to match process needs for selective binding characteristics, and they document batch histories in accordance with agrochemical industry standards for downstream registration filings.

    Industry compliance standards

    • FAO/WHO Specifications for Pesticide Quality Control
    • OECD Good Laboratory Practice (GLP) for Industrial Studies
    • China ICAMA Registration Guidelines
    • BPR (EU Regulation 528/2012) for biocidal products

    Typical usage ratio

    • Usually 1–3% by weight in the active ingredient precursor stage, with dosage tailored to the specific molecule being synthesized and potency requirements

    Downstream process integration

    • Introduced post-ketone coupling and prior to alkylation step, typically in high-pressure stirred reactors with real-time analytic monitoring

    Final product types

    • Triazole fungicide technical concentrates
    • Fluorinated sulfonylurea herbicides
    • Pyridine-carboxylic acid herbicide actives

    3. Electronic Chemicals (OLED and Display Materials)

    Producers of high-performance display and semiconductor components use the compound to functionalize aryl-based intermediates for organic light-emitting diode (OLED) materials and other fluorinated aromatic monomers. Chemical integration is tightly controlled to ensure downstream compatibility with complex deposition and fabrication steps essential for electronic device durability.

    Industry compliance standards

    • IEC 62474 Material Declaration for Electronic Industry
    • RoHS Directive (EU 2011/65/EU) Substances Restrictions
    • Semiconductor Equipment and Materials International (SEMI) S2 Safety Guidelines
    • ISO 9001:2015 for electronics chemical production

    Typical usage ratio

    • Added at 0.2-1% by mass depending on the molecular design of the electronic polymer backbone and film thickness requirements

    Downstream process integration

    • Input as a key reagent during Suzuki coupling or direct arylation polymerization in precisely regulated inert atmosphere systems before substrate coating

    Final product types

    • Fluorinated OLED emitter molecules
    • High-resistance display backplanes
    • Organic transistor grade intermediates

    4. Fine Chemical Synthesis (Custom Fluorinated Building Blocks)

    Specialty chemical manufacturers employ this compound as a pivotal building block for assembling diverse fluorinated structures used in dyes, functionalized monomers, and analytical reagent synthesis. The controlled addition routes allow tight tuning of molecular architecture, critical for downstream processes where performance and regulatory auditing converge at customer-established acceptance criteria.

    Industry compliance standards

    • REACH (Regulation EC No 1907/2006) for chemical safety
    • ISO 14001 Environmental Management for chemical processes
    • Japan CSCL Regulation for Industrial Chemicals
    • GHS (UN Globally Harmonized System) Labeling and Documentation

    Typical usage ratio

    • Ranges from 0.5–3% by molar equivalent in final product formulations, based on target compound structure and functional group requirements

    Downstream process integration

    • Fed into step-growth synthesis cycles, most often following nitrile functionalization and preceding condensation or cyclization, within jacketed glass reactors under monitored atmosphere

    Final product types

    • Fluorinated azo dyes
    • Specialized analytical standards
    • Customized monomer blocks for advanced material R&D
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