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2,3,6-Trifluorobenzonitrile

    • Product Name 2,3,6-Trifluorobenzonitrile
    • Alias 2,3,6-Trifluorobenzonitrile
    • Einecs 212-551-4
    • 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

    855084

    Cas Number 23256-30-6
    Molecular Formula C7H2F3N
    Molecular Weight 157.09 g/mol
    Iupac Name 2,3,6-Trifluorobenzonitrile
    Appearance White to light yellow solid
    Melting Point 38-42°C
    Boiling Point 193-195°C
    Density 1.40 g/cm3
    Solubility In Water Slightly soluble
    Purity Typically ≥98%
    Smiles C1=C(C=C(C(=C1F)F)C#N)F
    Refractive Index 1.494 (predicted)
    Flash Point 77°C (closed cup)
    Storage Condition Store in a cool, dry, and well-ventilated place

    As an accredited 2,3,6-Trifluorobenzonitrile factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 100g of 2,3,6-Trifluorobenzonitrile is supplied in a sealed amber glass bottle with a tamper-evident cap and warning label.
    Shipping 2,3,6-Trifluorobenzonitrile is shipped in tightly sealed containers, protected from moisture and light. It should be transported according to local, national, and international regulations for hazardous chemicals. Ensure proper labeling and documentation. Avoid excessive heat and handle with appropriate safety equipment to minimize exposure risk during transit. Store in a cool, well-ventilated area.
    Storage 2,3,6-Trifluorobenzonitrile should be stored in a tightly sealed container in a cool, dry, and well-ventilated area, away from heat and sources of ignition. Keep it separate from incompatible substances such as strong oxidants and acids. Store in a designated chemical storage cabinet, preferably suitable for organics, and ensure proper labeling. Avoid exposure to moisture and direct sunlight.
    Application of 2,3,6-Trifluorobenzonitrile

    Applications of 2,3,6-Trifluorobenzonitrile in Industrial Manufacturing

    2,3,6-Trifluorobenzonitrile plays a pivotal role as an intermediate in the synthesis of high-value specialty chemicals. Our factory supplies this raw material directly for advanced industrial applications, focusing on strict customer requirements for quality and compliance. Below, we outline principal downstream uses in detail, covering process, compliance, dosage, and finished product considerations based on real manufacturer feedback and global industry practice.

    1. Active Pharmaceutical Ingredient (API) Intermediate Synthesis

    This material is widely adopted as a key fluorinated aromatic building block by pharmaceutical manufacturers. It is used specifically in the multi-step synthesis of APIs for treatments in neurology and oncology sectors. Chemical engineers integrate the compound during early stages of synthetic routes to enable unique fluorine substitution patterns in drug targets, supporting metabolic stability and bioavailability requirements. Production batches strictly align with customer validation standards imposed by regulatory authorities due to the critical impact on API purity and structure.

    Industry compliance standards

    • ICH Q7 – Good Manufacturing Practice (GMP) for Active Pharmaceutical Ingredients
    • USP/NF monographs (where applicable)
    • EU Guidelines for Good Manufacturing Practice for Medicinal Products for Human Use
    • 21 CFR Parts 210/211 – US FDA cGMP for Finished Pharmaceuticals

    Typical usage ratio

    • Formulators use loading levels between 0.7 to 1.8 molar equivalents per synthetic step. Ratio adjustment depends on route optimization, target molecule structure, and impurity control specifications agreed by the client’s process development team.

    Downstream process integration

    • Material is introduced during aromatic ring construction or fluorination coupling stages, often as a nucleophilic partner or halogenated intermediate. Reactors require inert atmosphere. Accuracy in charge rate and sequence impacts pharmacological activity profiling downstream.

    Final product types

    • Fluorinated active pharmaceutical ingredients, e.g., kinase inhibitors, antipsychotics, or targeted anti-cancer drugs
    • Clinical development bulk compounds

    2. Agrochemical Intermediate for Herbicide Synthesis

    Downstream manufacturers utilize 2,3,6-trifluorobenzonitrile as a strategic intermediate in synthesizing innovative herbicidal active ingredients, particularly those relying on electron-deficient aromatic cores. The compound enables site-selective fluorination required in the development of both pre- and post-emergent weed control products. High purity index and traceability from our production are critical for multi-ton scale blending by agrochemical formulators who must comply with strict residue and contaminant limits set for crop protection chemicals.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • OECD Guidelines for the Testing of Chemicals
    • ISO 9001:2015 Quality Management System for chemical manufacture and batch records
    • REACH (Registration, Evaluation, Authorisation and Restriction of Chemicals) – EU compliance

    Typical usage ratio

    • Depending on herbicide core structure, use ranges from 0.6 to 1.2 equivalents in coupling or ring closure reactions. Adjustments follow target ingredient synthesis pathway, seasonal throughput, and downstream crop registration requirements.

    Downstream process integration

    • Applied during early-stage arylation, then transitioned through halide exchange, reduction, or amination steps within closed-vessel systems. Timing and batch control are monitored with in-process HPLC assays to ensure compliance for food chain safety certifications.

    Final product types

    • Trifluoro-substituted herbicide actives (e.g., for cereals, maize, and soybean crops)
    • Bulk technical concentrates for registration under international pesticide regulations

    3. Liquid Crystal Display (LCD) Intermediate Material

    Manufacturers in the advanced materials sector employ this compound as a critical starting material in the creation of high-performance liquid crystal monomers. Its multiple fluorine substitutions offer precision molecular tuning for low viscosity and enhanced electro-optical response in panel and display fabrication. Consistent quality control allows our partners to meet global requirements for electronic component mass production, with in-line testing performed at every batch transfer point.

    Industry compliance standards

    • IPC-6012 – Qualification and Performance Specification for Rigid Printed Boards
    • IEC 61249 – Materials for Printed Boards and Other Interconnecting Structures
    • RoHS 3 (EU Directive 2015/863) – Restriction of Hazardous Substances
    • ISO 14001:2015 for environmental management in electronics manufacturing

    Typical usage ratio

    • Added between 5% to 15% by weight to the aromatic core feedstock in monomer blend formulations. Dosing is managed to achieve target birefringence and dielectric thresholds as specified by display device OEM performance protocols.

    Downstream process integration

    • Material enters pre-polymerization tanks or fluorination reactors as an initial charge. Inline viscosity and color testing ensure batch reproducibility. Post-reaction filtrations remove trace byproducts prior to integration in subsequent monomer design steps.

    Final product types

    • High-purity fluorinated monomers and oligomers for LCD panel production
    • Processed liquid crystal blends for TFT and OLED display segments

    4. Specialty Polymer Synthesis for Engineering Plastics

    Chemical processing companies engaged in specialty polymer synthesis select this fluorinated nitrile as a reactive intermediate for polyaryletherketone and polyaryl ether sulfone platforms. The building block’s specific substitution enables engineered plastics with improved flame resistance and chemical durability, suitable for aerospace, automotive, and electronics industries. In-line spectrometry and microtrace analysis at our plant validate every production campaign to support customer qualification for high-value molding compounds.

    Industry compliance standards

    • UL 94 – Standard for Safety of Flammability of Plastic Materials
    • ASTM D5208 – Standard Practice for Fluoropolymer Plastics
    • ISO 9001:2015 for polymer batch traceability
    • REACH authorization for polymer building block usage

    Typical usage ratio

    • Added at 0.5 to 3.0 mol% to the total reaction mixture, depending on chain extension length and targeted mechanical performance indices. Dosing is adjusted per engineering requirements from customer technical datasheets.

    Downstream process integration

    • Incorporated during initial polymerization/copolymerization. The introduction timing, under monitored temperature ramp-up, controls chain distribution and final thermomechanical stability as verified by size-exclusion chromatography.

    Final product types

    • Heat-resistant fluoropolymer resins
    • Compounded pellets for injection molding, extrusion, or 3D printing

    5. Fine Chemical Intermediate for Dye and Pigment Manufacture

    Producers of performance dyes and pigments adopt this nitrile derivative for controlled aromatic fluorination in colorant synthesis. Its role as a precursor underpins molecular tailoring of lightfastness, weatherability, and chemical resistance properties in both organic dyes and specialty pigments. Customer auditing of our trace-level impurities ensures clean transition into chromophore development and end-use compliance in automotive coatings, plastics coloration, and digital printing inks.

    Industry compliance standards

    • ISO 787/1 – General Methods of Testing Pigments and Extenders
    • EN 71-3 – Safety of Toys, migration of certain elements (for pigments in children’s products)
    • ETAD – Ecological and Toxicological Association of Dyes and Organic Pigments Manufacturers
    • GMP for colorants in food contact plastics (EU 2023/2006 as applicable)

    Typical usage ratio

    • Standard additions range from 1% to 8% by molecular weight in precursor feed, dependent on pigment/dye class and desired chromatic performance metrics. Adjustments reflect solvent system, batch scale, and regulatory limit thresholds for final use.

    Downstream process integration

    • Material is charged into the initial condensation or coupling reaction vessel. Purity and feed timing affect color strength and final hue stability. Integration includes solvent selection and temperature programming for maximal colorant yield and purity.

    Final product types

    • Fluorinated azo and anthraquinone dyes for plastics and fibers
    • Specialty pigments for coatings, high-resolution printing inks, and mass colorants
    Free Quote

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