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4,4,4-Trifluorocrotonitrile

    • Product Name 4,4,4-Trifluorocrotonitrile
    • Alias Trifluorocrotononitrile
    • Einecs 684-010-9
    • 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

    374218

    Product Name 4,4,4-Trifluorocrotonitrile
    Cas Number 406-94-0
    Molecular Formula C4H2F3N
    Molecular Weight 121.06
    Appearance Colorless liquid
    Boiling Point 84-86°C
    Density 1.224 g/mL at 25°C
    Refractive Index 1.338
    Flash Point 18°C
    Smiles C=CC(C#N)(F)F
    Inchi InChI=1S/C4H2F3N/c1-2-3(4(5,6)7)8/h2-3H,1H2
    Solubility Slightly soluble in water

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

    Packing & Storage
    Packing The chemical, 4,4,4-Trifluorocrotonitrile, is packaged in a 25-gram amber glass bottle with a secure screw cap.
    Shipping **4,4,4-Trifluorocrotonitrile** should be shipped in tightly sealed containers, protected from moisture and incompatible substances. Transport in accordance with local, national, and international regulations for hazardous chemicals. Use appropriate labeling and documentation. Ensure chemical compatibility of packaging materials and avoid exposure to heat, sparks, and open flames during transit.
    Storage 4,4,4-Trifluorocrotonitrile should be stored in a cool, dry, well-ventilated area, away from sources of ignition and moisture. Keep the container tightly closed and protected from direct sunlight. Store separately from incompatible materials such as strong acids, bases, and oxidizing agents. Use appropriate chemical storage containers, clearly labeled, and follow local regulations for toxic and volatile substances.
    Application of 4,4,4-Trifluorocrotonitrile

    Applications of 4,4,4-Trifluorocrotonitrile in Industrial Manufacturing

    As the original manufacturer of 4,4,4-Trifluorocrotonitrile, we supply this specialty intermediate for critical downstream chemical syntheses. Below are specific industrial segments that integrate this compound, each with their own compliance, blending, process, and end-use requirements.

    1. Agrochemical Active Ingredient Synthesis

    Agrochemical manufacturers use 4,4,4-Trifluorocrotonitrile as a unique trifluoromethyl building block to introduce a trifluoromethylated nitrile motif into herbicide and insecticide molecules. Its usage appears in the nucleophilic addition stage for synthesizing specific pyridine-based actives, where precise control of reactivity and purity is needed. Downstream processors carefully manage residual levels and by-products to comply with national pesticide residue limits for finished agrochemical formulations.

    Industry compliance standards

    • EU Regulation No 1107/2009 (plant protection products)
    • US EPA CFR Title 40 (pesticide registration)
    • ISO 9001:2015 Quality Management Systems
    • China GB 2763 pesticide MRLs

    Typical usage ratio

    • 3–10% by molar ratio per batch, adjusted by target molecule requirements and target conversion yield

    Downstream process integration

    • Reacts in early-stage condensation or nucleophilic addition steps, prior to heterocycle formation or halogenation

    Final product types

    • Trifluoromethyl-substituted herbicides
    • Systemic insecticides for crop protection
    • Pre-emergent weed control agents

    2. Pharmaceutical Intermediate Production

    Active pharmaceutical ingredient (API) manufacturers select 4,4,4-Trifluorocrotonitrile to create novel trifluoromethylated scaffolds for next-generation drug candidates, especially in oncology and metabolic disorder compounds. The compound acts as a key intermediate in multi-step synthesis, entering amidation or reduction reactions to build molecular complexity. GMP production requires strict impurity profiling and lot traceability throughout synthesis and purification workflow.

    Industry compliance standards

    • ICH Q7 and Q11 for API manufacturing
    • EU GMP Part II (ICH Q7)
    • US FDA 21 CFR 210/211 for pharmaceuticals
    • USP/NF and Ph. Eur. monographs as applicable

    Typical usage ratio

    • Mol% input varies from 5–15% in main synthetic transformations, based on targeted API structure and downstream step conversion rates

    Downstream process integration

    • Initial or mid-stage input for carbon–carbon or carbon–nitrogen bond formation, followed by reduction, hydrolysis, or ring closure operations

    Final product types

    • Clinical and pre-clinical small molecule drug candidates
    • Final APIs with trifluoromethylated features
    • Trifluoromethylpyridine intermediates

    3. Fluorinated Fine Chemical Manufacturing

    Producers of specialty fine chemicals utilize 4,4,4-Trifluorocrotonitrile to construct molecular frameworks in high-value fluorinated materials. Applications include surface-active agents, advanced polymers, and electronics chemicals where robust trifluoromethyl chemistry imparts chemical and thermal resistance. Quality assurance teams maintain batch records per ISO and REACH obligations, closely monitoring halide and moisture contamination levels.

    Industry compliance standards

    • REACH Registration (EC)
    • ISO 14001:2015 (Environmental Management)
    • Japanese Chemical Substances Control Law
    • UL Materials Certification for electronics additives

    Typical usage ratio

    • 1–6% by mass as a reactive intermediate, varied per product formulation and chain length targets

    Downstream process integration

    • Feeds into alkylation or addition reactions; introduced during oligomer synthesis or chain-end group modification steps

    Final product types

    • Fluorinated specialty monomers
    • High-performance surface coatings
    • Hydrophobic polymer additives

    4. Synthesis of Fluorinated Heterocyclic Compounds

    Chemical synthesis companies employ 4,4,4-Trifluorocrotonitrile to introduce the trifluoromethyl group into nitrogen or oxygen heterocycles. This application appears in research-driven and production-scale synthesis of advanced materials, where the raw material acts as a substrate in cyclization or cycloaddition steps. Rigorous control of reaction temperature and stoichiometry is standard due to exothermic behavior and selectivity requirements.

    Industry compliance standards

    • GHS Hazard Classification for handling
    • Responsible Care® chemical management
    • ISO 9001:2015 for process traceability
    • Local hazardous chemical manufacturer regulations

    Typical usage ratio

    • Varies: 2–8 mole % per batch depending on desired ring structure and substitution pattern

    Downstream process integration

    • Introduced as a coupling partner in cyclization or base-catalyzed annulation steps

    Final product types

    • Trifluoromethylated pyridines and pyrimidines
    • Drug discovery heterocycle libraries
    • Functional specialty chemicals for electronics

    5. Custom Synthesis for Advanced Material R&D

    Contract research and production organizations (CRO/CMO) employ 4,4,4-Trifluorocrotonitrile in the development of new functional materials including liquid crystals, performance surfactants, and optoelectronic intermediates. Research chemists specify this reagent for selective installation of trifluoromethyl groups in exploratory synthesis. Every batch must include CoA-supported NMR and GC analysis results, and full traceability according to project and customer confidentiality rules.

    Industry compliance standards

    • ISO 9001:2015 for analytical verification
    • GLP (Good Laboratory Practice) for R&D syntheses
    • Material Handling per OSHA CFR 1910.1200 (USA)
    • Non-Disclosure Agreements for client projects

    Typical usage ratio

    • 0.5–5 mol% relative to starting substrate, tunable in small-scale synthesis and pilot campaigns

    Downstream process integration

    • Used in early-stage or final step substitutions and cyclizations, often as a key structural differentiator in R&D compounds

    Final product types

    • Research-scale fluorinated material samples
    • Custom-designed active intermediates
    • Performance additives for liquid crystal and display applications
    Free Quote

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