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2-[4-[2-Nitro-4-(Trifluoromethyl)Phenyl]Piperazino]-1-Ethanol

    • Product Name 2-[4-[2-Nitro-4-(Trifluoromethyl)Phenyl]Piperazino]-1-Ethanol
    • Alias NPTP
    • Einecs 629-022-6
    • 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

    385337

    Chemical Name 2-[4-[2-Nitro-4-(Trifluoromethyl)Phenyl]Piperazino]-1-Ethanol
    Molecular Formula C13H16F3N3O3
    Molecular Weight 319.28 g/mol
    Appearance Solid
    Color Off-white to yellow
    Solubility Soluble in DMSO
    Smiles C1CN(CCN1C2=CC=C(C=C2[N+](=O)[O-])C(F)(F)F)CCO
    Purity Typically ≥98%
    Storage Conditions Store at -20°C, protected from light

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

    Packing & Storage
    Packing Amber glass bottle with tamper-evident cap, chemical label, hazard pictograms; contains 25 grams of 2-[4-[2-Nitro-4-(Trifluoromethyl)Phenyl]Piperazino]-1-Ethanol.
    Shipping **Shipping Description:** 2-[4-[2-Nitro-4-(Trifluoromethyl)Phenyl]Piperazino]-1-Ethanol is shipped in tightly sealed containers, protected from light and moisture. It is transported as a chemical substance, possibly requiring classification as a hazardous material. Standard shipping includes appropriate labeling and documentation, ensuring compliance with IATA, DOT, and international chemical transport regulations.
    Storage Store **2-[4-[2-Nitro-4-(trifluoromethyl)phenyl]piperazino]-1-ethanol** in a tightly sealed container, protected from light, moisture, and incompatible substances. Keep at 2–8°C (refrigerated) in a well-ventilated chemical storage area. Avoid sources of ignition and strong oxidizers. Ensure proper labeling and restrict access to trained personnel. Follow all institutional and regulatory guidelines for storage of hazardous chemicals.
    Application of 2-[4-[2-Nitro-4-(Trifluoromethyl)Phenyl]Piperazino]-1-Ethanol

    Applications of 2-[4-[2-Nitro-4-(Trifluoromethyl)Phenyl]Piperazino]-1-Ethanol in Industrial Manufacturing

    Our production of 2-[4-[2-Nitro-4-(Trifluoromethyl)Phenyl]Piperazino]-1-Ethanol supports specialized downstream sectors requiring nitrogen- and fluorine-bearing building blocks. The material is processed under strict quality controls to ensure compatibility with exacting industry requirements. Below are key fields where our product serves as a critical component in industrial formulations and synthesis.

    1. Active Pharmaceutical Ingredient (API) Synthesis

    This substance frequently appears as an intermediate in the synthesis of advanced pharmaceuticals, particularly within CNS-active and anti-inflammatory drug research. Its piperazine and aromatic nitro functionalities allow targeted modifications for medicinal lead compounds. Pharmaceutical manufacturers employ this intermediate in various multi-step reactions to access regulated, high-value small molecules.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • United States Pharmacopeia (USP)
    • European Pharmacopoeia (EP)
    • China National Medical Products Administration (NMPA) requirements

    Typical usage ratio

    • 0.5–5 molar equivalents relative to target API core, depending on reaction path optimization; precise use determined by process route and purity targets

    Downstream process integration

    • Added during heterocycle coupling or nitroaromatic substitution stage
    • Processed in GMP-compliant reactor trains
    • Combined with reducing agents or alkylating reagents in batch or flow steps

    Final product types

    • Antipsychotic agents
    • Novel CNS drugs
    • Custom medicinal chemistry scaffolds
    • Patent-protected pharmaceutical intermediates

    2. Agrochemical Active Compound Synthesis

    Major agrochemical formulators utilize this molecule as a specialty intermediate in the preparation of piperazine-based herbicides and fungicides. The electron-withdrawing nitro and trifluoromethyl substituents allow for selective substitutions and enable improved bioactivity for next-generation crop protection agents.

    Industry compliance standards

    • FAO/WHO specifications for pesticide active ingredients
    • REACH registration for agricultural chemicals (Europe)
    • US EPA’s Office of Pesticide Programs (OPP) regulations
    • China Hazardous Chemicals Registration (SAWS)

    Typical usage ratio

    • 5–12% by weight within key reaction steps, depending on synthesis yield and crop protection target requirements

    Downstream process integration

    • Reacted during key N-alkylation or aryl substitution stages in the synthesis of piperazine-based actives
    • Introduced in solvent-based downstream blending or stepwise multi-stage synthesis under controlled temperature and agitation

    Final product types

    • Herbicide active ingredients
    • Fungicide active intermediates
    • Pre-formulated crop protection compounds
    • Registered plant health products

    3. Advanced Material Monomer Synthesis

    The compound provides a crucial fluorinated building block in the formulation of specialty polymers and coatings demanding enhanced chemical and thermal resistance. Material manufacturers value the stability conferred by the nitro and trifluoromethyl groups in high-performance resins as used in electronics, aerospace, or membrane technologies.

    Industry compliance standards

    • ISO 9001-certified Quality Management for Polymer Production
    • RoHS Directive (2011/65/EU) for end-use in electronics
    • REACH requirements for polymer monomers
    • UL 94 flame retardancy testing for final products

    Typical usage ratio

    • 3–8% by weight in specialty monomer feeds; proportion adjusted according to crosslink density and product property targets

    Downstream process integration

    • Dosed into initial resin or copolymer batch
    • Incorporated via controlled addition with other monomers under elevated temperature and inert atmosphere
    • Managed with in-line QC to monitor polymerization progress

    Final product types

    • Fluorinated polymers for electronics encapsulation
    • Specialty coatings with enhanced solvent resistance
    • Polymeric membranes for gas separation
    • High-durability composite materials

    4. Specialty Dye and Pigment Precursor Manufacturing

    This raw material acts as a strategic precursor in synthesizing high-value dyes and pigments, where electron-rich and electron-deficient groups modulate absorption and photostability. Dye manufacturers introduce it in tailored coupling reactions to access vibrant colors or high-stability pigments for plastics and inks.

    Industry compliance standards

    • ISO 9001 and ISO 14001 for colorant production
    • EU REACH Annex XIV (for pigments)
    • US FDA regulations for color additives in plastics packaging (21 CFR 178.3297, where applicable)
    • EN 71-3 Safety standards for toy colorants

    Typical usage ratio

    • 2–7% by weight of reaction mass; altered depending on final pigment concentration and desired hue intensity

    Downstream process integration

    • Added in azo coupling or aromatic condensation steps during dye manufacture
    • Processed in stainless steel kettles with precise temperature control and pH adjustment

    Final product types

    • High-durability plastic colorants
    • Specialty printing inks
    • Functional pigments for optoelectronic applications
    • Long-life textile dyes
    Free Quote

    Competitive 2-[4-[2-Nitro-4-(Trifluoromethyl)Phenyl]Piperazino]-1-Ethanol prices that fit your budget—flexible terms and customized quotes for every order.

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