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3-(Trifluoromethyl)Phenethylamine

    • Product Name 3-(Trifluoromethyl)Phenethylamine
    • Alias 3-(Trifluoromethyl)-2-phenylethanamine
    • Einecs 620-556-3
    • 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

    336070

    Chemical Name 3-(Trifluoromethyl)phenethylamine
    Molecular Formula C9H10F3N
    Molecular Weight 189.18 g/mol
    Cas Number 368-39-8
    Appearance Colorless to pale yellow liquid
    Boiling Point 83-85°C at 3 mmHg
    Density 1.211 g/cm³
    Melting Point -30°C
    Solubility Slightly soluble in water; soluble in organic solvents
    Synonyms m-(Trifluoromethyl)phenethylamine
    Smiles CC(N)CC1=CC(=CC=C1)C(F)(F)F
    Inchi InChI=1S/C9H10F3N/c10-9(11,12)8-3-1-2-7(6-8)4-5-13/h1-3,6H,4-5,13H2

    As an accredited 3-(Trifluoromethyl)Phenethylamine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle, 100g, equipped with screw cap and tamper-evident seal, labeled with hazard warnings and chemical identification details.
    Shipping 3-(Trifluoromethyl)Phenethylamine is shipped in secure, leak-proof containers compliant with regulatory guidelines. Packaging ensures protection from moisture, light, and contamination. The chemical is clearly labeled, and transport follows all safety procedures for handling hazardous substances. Shipping is typically done via certified chemical couriers, adhering to local and international regulations.
    Storage 3-(Trifluoromethyl)phenethylamine should be stored in a tightly sealed container, kept in a cool, dry, and well-ventilated area, away from direct sunlight and sources of ignition. Store separately from oxidizing agents and strong acids. Ensure the storage area is equipped with appropriate spill containment and clearly labeled. Use appropriate personal protective equipment when handling the chemical to prevent exposure.
    Application of 3-(Trifluoromethyl)Phenethylamine

    Applications of 3-(Trifluoromethyl)Phenethylamine in Industrial Manufacturing

    Our direct manufacturing supply of 3-(Trifluoromethyl)Phenethylamine addresses the key requirements of leading value-chain sectors, where this advanced fluorinated amine finds defined functional uses in specialty chemicals and APIs. The following application scenarios summarize authentic downstream integrations, specifying compliance, formulation guidance, production positioning, and concrete end products.

    1. Pharmaceutical Intermediate for CNS Active Compound Synthesis

    API producers in the central nervous system (CNS) therapy field incorporate this amine to construct trifluoromethylated phenethylamine frameworks, supporting the development of innovative psychoactive agents and antidepressant APIs. The compound is reacted during late-stage building block coupling, offering rapid access to target molecules under strict GMP frameworks required for active pharmaceutical ingredient manufacturing.

    Industry compliance standards

    • ICH Q7: Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • 21 CFR Parts 210/211: US FDA CGMP
    • EU GMP Part II
    • Ph. Eur., USP monographs for relevant APIs

    Typical usage ratio

    • Utilized at 0.10–0.35 molar equivalents, depending on target molecule synthesis pathway and desired yield optimization

    Downstream process integration

    • Employed during the fragment coupling or substitution step in multi-stage batch or continuous flow synthesis of CNS drug candidates

    Final product types

    • Novel antidepressant active ingredients
    • Trifluoromethylated CNS drug compounds
    • Research grade API intermediates

    2. Agrochemical Synthesis: Herbicide Intermediate Manufacturing

    Agrochemical formulators require fluoroaromatic amines as advanced intermediates for selective herbicide molecule development. The compound is reacted to generate essential structural motifs in triazine and other branded post-emergent herbicides, satisfying regulatory documentation for precursor traceability and batch consistency demanded by crop protection companies.

    Industry compliance standards

    • FAO/WHO Technical Specifications for Pesticides
    • ISO 9001 quality system for chemical production
    • REACH (EC 1907/2006) for intermediate registration
    • China National Standards for Agrochemical Intermediates

    Typical usage ratio

    • Incorporated at 1.2–1.5 stoichiometric equivalents per target herbicide batch; adjusted to conversion efficiency and downstream purification requirements

    Downstream process integration

    • Added during scale-up step for nucleophilic aromatic substitution as a functionalized building block contributing to herbicide active core

    Final product types

    • Trifluoromethyl-substituted triazine herbicides
    • Selective post-emergence crop protection actives
    • Custom-formulated active ingredient intermediates

    3. Advanced Materials: Monomer for Specialty Polymer Synthesis

    Manufacturers of high-performance polymers introduce this compound as a monomer to impart fluorinated functionality for thermal and chemical resistance enhancements. Specialty polyamides and co-polymers derived with this raw material find application in engineering plastics, providing tailored physical characteristics for downstream electrical, automotive, and industrial device housings.

    Industry compliance standards

    • ISO 9001 for specialty chemical and polymer production
    • ASTM D638/D790 for mechanical testing
    • RoHS compliance for polymer additives in electronics
    • REACH registration for new monomers

    Typical usage ratio

    • Monomer charge levels in the range of 2–10% by mole in overall monomer feed; adjusted for property tuning based on end-use performance requirements

    Downstream process integration

    • Dosed into the initial polymerization reactor charge, often via solution or bulk polymerization schemes to co-polymerize with other amine or acid monomers

    Final product types

    • Fluorinated specialty polyamides
    • Co-polymer resins for automotive electronics
    • Engineering plastics with enhanced resistance to chemicals

    4. Organic Electronic Materials: Precursor for OLED/Electroluminescent Chemicals

    Organic electronics R&D and specialty chemical suppliers adopt trifluoromethylated phenethylamines as key starting points in the synthesis of electron-transport and hole-blocking molecules, which are incorporated into OLED and EL device structures. The amine’s substitution pattern is leveraged to modulate energy levels and stability for improved device longevity, with strict production traceability per optoelectronics supply guidelines.

    Industry compliance standards

    • ISO 17025 analytical documentation for specialty materials
    • RoHS directive for electronic components
    • REACH substance identification for R&D substances
    • Supplier-specific optoelectronic purity protocols

    Typical usage ratio

    • Integrated at concentrations of 1–5 wt% of precursor feedstock in layered organic electronic chemical syntheses; modified by target performance and purity controls

    Downstream process integration

    • Fed into multi-step synthesis at electron-donating group installation or as a side chain functionalization during organic semiconductor batch production

    Final product types

    • Electron transport layer compounds for OLEDs
    • Trifluoromethylated charge transport molecules
    • Electroluminescent material intermediates

    5. Fine Chemical Synthesis: Reference Standard and Analytical Building Block

    Chemical reference laboratories and analytical standards manufacturers use the compound for preparation of certified reference materials and for structural elucidation in mass spectrometry calibration. High-purity batches enter production flows for analytical standards that underpin regulatory submissions, impurity profiling, and method validation in pharmaceutical and environmental labs.

    Industry compliance standards

    • ISO 17034 for reference material producers
    • Good Laboratory Practice (GLP) for analytical standards
    • USP and EP guidelines for reference standards preparation
    • Traceable certificate documentation per ISO/IEC 17025

    Typical usage ratio

    • Charged at 100 wt% (neat) for standard preparation; diluted to 1–10 ppm or mg/L depending on analytical calibration requirements

    Downstream process integration

    • Dissolved in high-purity solvents and aliquoted into certified vials during gravimetric and volumetric reference standard preparation

    Final product types

    • Certified neat standards for mass spectrometry
    • Analytical calibration solutions
    • Structural reference markers for impurity profiling
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