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5-(Trifluoromethyl)Pyridin-2-Amine

    • Product Name 5-(Trifluoromethyl)Pyridin-2-Amine
    • Alias 5-(Trifluoromethyl)-2-aminopyridine
    • Einecs 821-736-7
    • 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

    602039

    Product Name 5-(Trifluoromethyl)Pyridin-2-Amine
    Cas Number 86483-91-4
    Molecular Formula C6H5F3N2
    Molecular Weight 162.12 g/mol
    Appearance White to off-white solid
    Melting Point 48-52°C
    Purity Typically ≥97%
    Solubility Soluble in organic solvents (e.g., DMSO, DMF)
    Smiles C1=CC(=NC=C1N)C(F)(F)F
    Inchi InChI=1S/C6H5F3N2/c7-6(8,9)4-2-1-3-11-5(4)10/h1-3H,(H2,10,11)
    Synonyms 2-Amino-5-(trifluoromethyl)pyridine
    Storage Conditions Store at 2-8°C, protected from light and moisture

    As an accredited 5-(Trifluoromethyl)Pyridin-2-Amine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing A 25g amber glass bottle with a tightly sealed cap, labeled "5-(Trifluoromethyl)Pyridin-2-Amine," including safety and handling information.
    Shipping 5-(Trifluoromethyl)Pyridin-2-Amine is shipped in tightly sealed containers, protected from moisture and light. It should be handled as a hazardous material, complying with appropriate chemical shipping regulations. Packaging is labeled for safe transport and includes all safety data. Shipping typically uses ground or air transport with hazardous material documentation.
    Storage Store **5-(Trifluoromethyl)pyridin-2-amine** in a cool, dry, well-ventilated area, tightly sealed in a chemical-resistant container. Keep away from incompatible substances such as strong oxidizers and acids. Protect from moisture and direct sunlight. Use within a fume hood if opened frequently and label clearly. Follow all relevant safety protocols for handling and storage of organic chemicals.
    Application of 5-(Trifluoromethyl)Pyridin-2-Amine

    Applications of 5-(Trifluoromethyl)Pyridin-2-Amine in Industrial Manufacturing

    As a primary producer, we supply 5-(Trifluoromethyl)Pyridin-2-Amine to leading industrial manufacturers working within regulated chemical sectors. This advanced intermediate acts as a core building block in regulated synthesis processes, directly supporting the production of compounds for agrochemical, pharmaceutical, and functional material markets worldwide.

    1. Agrochemical Active Ingredient Synthesis

    Multinational crop protection companies use this amine derivative to synthesize selective herbicides and fungicides. This compound introduces an electron-withdrawing trifluoromethyl group, which enhances the metabolic stability and bioactivity of active ingredients. Large-scale facilities employ it during the coupling and condensation stages, particularly for manufacturing pyridine-based pesticides. Quality control teams monitor trace impurity levels to comply with regulatory submissions and ensure process repeatability.

    Industry compliance standards

    • EU REACH (EC No 1907/2006) registration
    • US EPA FIFRA 40 CFR Part 158 for pesticide formulation
    • GB 2763-2021 Maximum Residue Limit Standards (China)
    • ISO 9001:2015 process quality system

    Typical usage ratio

    • 5–12% of the total reaction mass in condensation step, adjusted for desired substitution density and final product purity profiles

    Downstream process integration

    • Reacts as a core nucleophile in stepwise aromatic substitution and acylation, following in situ base activation during intermediate synthesis

    Final product types

    • Trifluoromethylpyridine-based herbicides (e.g., for rice, maize)
    • Pyridinic fungicides for high-value fruit and vegetable crops
    • Seed treatment actives targeting soil-borne pathogens

    2. Pharmaceutical Intermediate for Antiviral Compounds

    Branded and genetic drug substance manufacturers rely on this chemical as a structural intermediate in the development of specific antiviral agents. Its pyridine scaffold and electron-withdrawing group support lead optimization and scaffold modification during active pharmaceutical ingredient (API) synthesis. The material enters GMP-compliant synthesis suites, integrating with multi-step hydrogenation, protection, and deprotection procedures prior to purification and scaling.

    Industry compliance standards

    • ICH Q7A GMP for Active Pharmaceutical Ingredients
    • EDQM CEP (European Directorate for the Quality of Medicines)
    • US FDA 21 CFR Parts 210/211 for drug manufacturing
    • USP/NF analytical monograph traceability

    Typical usage ratio

    • 0.5–2.5 equivalents relative to starting substrate, titrated per route-specific yield optimization protocols

    Downstream process integration

    • Acylation and amination reactions during protected group synthesis in multi-step API assembly; followed by crystallization and HPLC purification

    Final product types

    • Pyridinyl-based antiviral drug APIs
    • Clinical trial material and registered starting materials (RSMs)
    • Proprietary pipeline intermediates for infectious disease pharmacotherapies

    3. Synthesis of Electronic Material Intermediates

    Specialty chemical companies integrate this amine intermediate into the synthesis of performance chemicals for electronics manufacturing. Its unique structure helps modify dielectric properties of precursors for OLED emitters, photoresists, and semiconducting polymers. Pilot and production lines dose this molecule in batch or continuous flow systems, following precise stoichiometric control managed via process analytics.

    Industry compliance standards

    • IEC 62474 for material declaration in electronics
    • RoHS Directive 2011/65/EU on hazardous substances
    • JIS Q 9100 (Japan) for quality management in electronics
    • ICP-MS verification for trace element control

    Typical usage ratio

    • 1–8 mol% in precursor feed; modulated according to target molecular weight and device performance characteristics

    Downstream process integration

    • Undergoes nucleophilic substitution and cross-coupling integrated after oligomerization steps, pre-purification for advanced materials assembly

    Final product types

    • Intermediate for high-performance OLED materials
    • Functionalized pyridine monomers for advanced polymers
    • Photoactive agents for photolithography and electronic imaging

    4. Intermediate for Specialty Dye and Pigment Manufacture

    Producers of high-value dyes and industrial pigments employ this amine in the formulation of solvent-stable, high-contrast colorants. Its trifluoromethyl-substituted structure confers enhanced electron density, supporting chromophore durability and environmental resistance in color applications. This specialty intermediate participates in diazotization and coupling reactions across controlled, closed-system production lines emphasizing reproducibility and color consistency.

    Industry compliance standards

    • CEN/TC 298 Colorant and Dye Chemical Testing (Europe)
    • ISO 787-24:1985 General Methods of Testing Pigments and Extenders
    • REACH Article 33 disclosure for SVHC
    • ASTM D4828-94 Dye Purity and Composition

    Typical usage ratio

    • 3–10% by weight in diazotization feed batch, adjusted for target absorbance coefficient and final product stability

    Downstream process integration

    • Forms the nucleophilic substrate during diazotization or direct aromatic coupling; followed by solvent extraction and milling for pigment grade standardization

    Final product types

    • Solvent-stable aromatic azo dyes
    • Highly durable pigment intermediates for plastics and coatings
    • Color formulations for industrial and automotive inks
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