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2-Amino-4-[3,5-Bis(Trifluoromethyl)Phenyl]Amino-1,3,5-Triazine

    • Product Name 2-Amino-4-[3,5-Bis(Trifluoromethyl)Phenyl]Amino-1,3,5-Triazine
    • Alias A-438079
    • Einecs NA
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry sales7@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    886731

    Chemical Name 2-Amino-4-[3,5-Bis(Trifluoromethyl)Phenyl]Amino-1,3,5-Triazine
    Molecular Formula C11H6F6N6
    Molecular Weight 340.20
    Cas Number 175278-17-8
    Appearance Off-white to light yellow solid
    Purity ≥98%
    Melting Point 226-229°C
    Solubility Slightly soluble in DMSO, DMF
    Storage Temperature 2-8°C
    Inchi InChI=1S/C11H6F6N6/c12-10(13)5-1-7(2-6(3-5)11(14,15)16)21-9-18-8(17)22-23-9/h1-3H,(H2,17,18,21,22,23)
    Smiles C1=C(C=C(C=C1Nc2nc(N)nc(n2)N)C(F)(F)F)C(F)(F)F

    As an accredited 2-Amino-4-[3,5-Bis(Trifluoromethyl)Phenyl]Amino-1,3,5-Triazine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The packaging is a sealed, amber glass bottle containing 25 grams of 2-Amino-4-[3,5-Bis(Trifluoromethyl)Phenyl]Amino-1,3,5-Triazine, labeled for laboratory use.
    Shipping 2-Amino-4-[3,5-Bis(Trifluoromethyl)Phenyl]Amino-1,3,5-Triazine is shipped in tightly sealed containers, protected from moisture and light. Transportation complies with chemical safety regulations, using appropriate labeling and documentation. Packages are padded to prevent breakage, and shipping is usually by ground or air freight, depending on destination and hazard classification.
    Storage Store 2-Amino-4-[3,5-bis(trifluoromethyl)phenyl]amino-1,3,5-triazine in a tightly sealed container, in a cool, dry, well-ventilated area away from heat, moisture, and incompatible substances such as strong acids or bases. Protect from direct sunlight. Use appropriate personal protective equipment when handling and avoid prolonged exposure. Store under inert atmosphere if sensitivity to air or moisture is suspected.
    Application of 2-Amino-4-[3,5-Bis(Trifluoromethyl)Phenyl]Amino-1,3,5-Triazine

    Applications of 2-Amino-4-[3,5-Bis(Trifluoromethyl)Phenyl]Amino-1,3,5-Triazine in Industrial Manufacturing

    Our facility directly synthesizes 2-Amino-4-[3,5-Bis(Trifluoromethyl)Phenyl]Amino-1,3,5-Triazine to serve advanced industrial customers in specialty downstream chemical sectors. Below, we offer a detailed outline of its real-world applications, covering unique compliance demands, practical usage ratios, relevant process stages, and the specific end products our customers manufacture.

    1. High-Performance Agricultural Fungicides

    This compound serves as an intermediate for the targeted synthesis of modern triazine-class fungicides, contributing to crop protection portfolios where high resistance to degradation and improved activity spectra are required. It enters the production stream for finely engineered pesticide actives tailored for regulated agricultural use.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • Regulation (EC) No. 1107/2009 concerning the placing of plant protection products on the market (EU)
    • China GB 2763-2021 Maximum Residue Limits for Pesticides in Foods
    • EPA FIFRA requirements (USA)

    Typical usage ratio

    • 1.5–4.0% (w/w) as a key intermediate in active ingredient synthesis; percentage fine-tuned based on targeted potency and downstream coupling requirements

    Downstream process integration

    • Introduced after initial triazine ring formation, used in SNAr (nucleophilic aromatic substitution) with suitable halogenated precursors, proceeding to final active substance crystallization and purification

    Final product types

    • Systemic cereal fungicides (e.g., for wheat, barley)
    • Seed treatment products
    • Protective grapevine and orchard fungicides
    • Specialized mixtures for broad-spectrum field applications

    2. Photostable UV Absorber Intermediates for Polymers

    Film and fiber producers use this triazine derivative in synthesizing UV absorber additives, especially for durable plastics and coatings exposed to intense sunlight. The chemical structure ensures strong resistance against photodegradation, making it suitable for engineering plastics sustaining harsh outdoor conditions.

    Industry compliance standards

    • REACH Regulation (EC) No. 1907/2006 (Annex XVII—restricted substances)
    • UL 746C Standard for Polymeric Materials—UV Exposure
    • ISO 4892-2:2013 Plastics—Methods of Exposure to Laboratory Light Sources
    • ASTM D5208—Standard Practice for Fluorescent UV Exposure of Photodegradable Plastics

    Typical usage ratio

    • 0.2–1.0% (w/w) in masterbatch synthesis; portion adjusted according to resin matrix (e.g., polycarbonate, PET, acrylics) and desired light fastness

    Downstream process integration

    • Feeds into condensation or transesterification stages with monomers or oligomers to generate functionalized UV absorber, followed by extrusion into polymer blend for granulation or direct molding

    Final product types

    • UV-resistant plastic films (e.g., greenhouse covers)
    • Automotive headlamp lenses
    • Exterior coatings for architectural applications
    • High-clarity synthetic fibers used in outdoor textiles

    3. Pharmaceutical Synthesis: Selective Kinase Inhibitor APIs

    This raw material is involved in the complex multi-step synthesis of advanced pharmaceutical ingredients, particularly in the development of novel triazine-based kinase inhibitors for oncology therapeutics. The compound’s unique substitution pattern facilitates selective binding characteristics in the assembled active pharmaceutical ingredient (API), impacting biological performance and regulatory acceptability.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP/EP/JP compendia requirements for traceability and purity
    • 21 CFR Part 211 (FDA US cGMP for Finished Pharmaceuticals)
    • Chinese Pharmacopoeia—Relevant API monograph controls

    Typical usage ratio

    • 0.5–2.2 molar equivalents per coupling step, precisely controlled based on target API molecular pathway and reaction scalability

    Downstream process integration

    • Employed during the intermediate coupling phase, using palladium-catalyzed cross-coupling or nucleophilic substitution, followed by protection/deprotection and purification under GMP

    Final product types

    • Investigational and commercial kinase inhibitor APIs
    • Reference standards for R&D and method validation
    • Advanced clinical trial materials
    • High-purity bulk substances for finished dosage manufacturing

    4. Specialty Dye Manufacturing for Technical Textiles

    This triazine derivative functions as a crucial coupling agent in synthesizing non-substantive, high-performance textile dyes where lightfastness, heat tolerance, and unique shade development are essential. It enables the development of dyes for demanding technical fabrics deployed in industrial sectors, especially where resistance to chemical and environmental stresses is critical.

    Industry compliance standards

    • Oeko-Tex Standard 100: Product Class I–IV (textile chemical safety)
    • ZDHC MRSL V3.0 (Zero Discharge of Hazardous Chemicals)
    • ISO 105-B02/B03: Methods of Test for Colour Fastness—Lightfastness
    • EU REACH Annex XVII: Textile Dye Limits

    Typical usage ratio

    • 0.4–1.6% (w/w) relative to total dye batch; increased for deeper shade requirements or additional functionalities such as washfastness

    Downstream process integration

    • Used in diazotization coupling or amidation with chromophoric precursors, then post-processed via spray-drying or crystallization to final dye concentrate

    Final product types

    • Solution-dyed performance fibers for automotive interiors
    • Flame-retardant workwear textiles
    • Outdoor awning and tent materials
    • Print inks for nonwovens and technical apparel

    5. Advanced Electronic Chemical Synthesis

    In the field of microelectronics, this triazine-based molecule acts as a precursor for photoresist additives, helping create pattern-defining coatings with improved etch resistance and thermal stability. The integration occurs in downstream formulations for semiconductor wafer processing, where stable pattern transfer is pivotal.

    Industry compliance standards

    • SEMATECH Technical Roadmap for Microelectronic Photoresists
    • RoHS Directive 2011/65/EU (electronic chemical restrictions)
    • GMP for Electronic Grade Chemical Manufacture (SEMI C93-0916)
    • ISO 9001:2015 (Quality Management for Materials Supply Chain)

    Typical usage ratio

    • 0.05–0.25% (w/w) in advanced chemically amplified photoresist blends; adjusted per lithography method and critical dimension requirements

    Downstream process integration

    • Added during pre-polymer or resist resin synthesis, followed by functional group introduction (e.g., diazonium, sulfonic acids), then microfiltration for cleanroom-grade purity

    Final product types

    • Photoresist coatings for semiconductor wafer fabrication
    • Advanced microlithography materials
    • Protective coatings for printed circuit boards
    • MOs (masking oxides) for high-density chip architectures

    6. High-End Coating Additives for Aerospace and Defense

    This chemical finds use as a performance modifier in aerospace-grade polyurethane and epoxy coatings. Formulators integrate it to reinforce chemical and UV resistance in coatings for aircraft exteriors and military hardware, where environmental endurance and material longevity are mandated by strict global standards.

    Industry compliance standards

    • AMS 3095A: Performance Requirements for Aviation Coatings
    • DEF STAN 80-161: MOD Specification for Paints and Finishes (UK MOD)
    • SAE Aerospace Standards AS22759 (cable insulation, related coating exposure)
    • REACH SVHC compliance for defense materials

    Typical usage ratio

    • 0.3–1.2% (w/w) within total formulation; ratio determined by performance verification through QUV accelerated weathering and thermal cycling tests

    Downstream process integration

    • Introduced during the pigment dispersion or binder extension phase, proceeding to cross-linking and final film formation, then tested under controlled humidity and salt-fog conditions for qualification

    Final product types

    • Aircraft exterior surface coatings
    • Anticorrosion coatings for military vehicles
    • Radar-absorbent materials (RAM) for stealth technology
    • Coating systems for aerospace fasteners and structural elements
    Free Quote

    Competitive 2-Amino-4-[3,5-Bis(Trifluoromethyl)Phenyl]Amino-1,3,5-Triazine prices that fit your budget—flexible terms and customized quotes for every order.

    For samples, pricing, or more information, please call us at +8615371019725 or mail to sales7@sinochem-nanjing.com.

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    Tel: +8615371019725

    Email: sales7@sinochem-nanjing.com

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