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4-(2,5-Diethoxy-4-Nitrophenyl)Morpholine

    • Product Name 4-(2,5-Diethoxy-4-Nitrophenyl)Morpholine
    • Alias Phenylmorpholine
    • Einecs 699-488-6
    • 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
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    Specifications

    HS Code

    409353

    Chemical Name 4-(2,5-Diethoxy-4-Nitrophenyl)Morpholine
    Molecular Formula C14H20N2O5
    Molecular Weight 296.32 g/mol
    Appearance Solid (likely yellow or orange)
    Solubility Soluble in organic solvents such as DMSO or ethanol
    Purity Typically ≥98% (when supplied commercially)
    Storage Conditions Store in a cool, dry place, protected from light
    Smiles CCOC1=CC(=C(N=CC1=O)OCC)[N+](=O)[O-]
    Iupac Name 4-(2,5-diethoxy-4-nitrophenyl)morpholine
    Synonyms 2,5-Diethoxy-4-nitrophenyl morpholine
    Hazard Statements May cause irritation to eyes, skin, and respiratory tract

    As an accredited 4-(2,5-Diethoxy-4-Nitrophenyl)Morpholine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle containing 50 grams, sealed with a screw cap, labeled with chemical name, CAS number, hazard symbols, and handling instructions.
    Shipping Shipping for **4-(2,5-Diethoxy-4-Nitrophenyl)Morpholine** is conducted in compliance with chemical safety regulations. The compound is securely packaged in airtight, chemical-resistant containers, clearly labeled with hazard information. All shipments include safety data sheets (SDS) and are transported via authorized couriers specializing in hazardous materials to ensure regulatory and environmental safety.
    Storage 4-(2,5-Diethoxy-4-Nitrophenyl)morpholine should be stored in a tightly closed container, away from direct sunlight and moisture, in a cool, dry, well-ventilated area. Avoid sources of heat and ignition, and segregate from incompatible substances such as strong oxidizers and acids. Clearly label the storage container, and ensure access is restricted to trained personnel.
    Application of 4-(2,5-Diethoxy-4-Nitrophenyl)Morpholine

    Applications of 4-(2,5-Diethoxy-4-Nitrophenyl)Morpholine in Industrial Manufacturing

    As a specialist manufacturer, we supply 4-(2,5-Diethoxy-4-Nitrophenyl)Morpholine directly to advanced chemical customers seeking precise performance across complex industrial syntheses. Below, we detail real-world downstream uses of this intermediate in regulated and technically demanding sectors, outlining dedicated scenario-specific requirements.

    1. High-Performance OLED Intermediate Synthesis

    This compound supports the synthesis of specialty intermediates for organic light-emitting diode (OLED) displays by contributing electronic properties essential for efficient light emission layers. Our customers utilize it during the manufacture of extended conjugated molecules, underpinning vivid and reliable visual technologies in premium devices.

    Industry compliance standards

    • RoHS 2015/863/EU (Restriction of Hazardous Substances for electronic components)
    • IEC 62474: Material declaration for electronic industry
    • QC: Material purity ≥99.0%, trace metals monitored per customer OLED grade specification

    Typical usage ratio

    • 0.6%–1.8% of total organic precursor batch, optimized for molar equivalence with target oligomer length

    Downstream process integration

    • Customers charge the raw material during the coupling step in the synthesis of light-emissive polymers or small molecules, following initial halogenation and catalyst addition

    Final product types

    • Light-emitting polymer chains for AMOLED display manufacture
    • Color-tuned OLED emitters used in smartwatches, smartphones, and premium TV panels

    2. Specialty Photoinitiator Manufacturing for UV-Curable Resins

    Customers employ this material in multi-step synthesis of high-absorption photoinitiators tailored for UV-cured inks and advanced coatings, where controlled nitroaromatic reactivity is critical for efficient photopolymerization and precise cure rates.

    Industry compliance standards

    • ISO 9001:2015 (Quality Management for chemicals)
    • REACH EC No 1907/2006 (European Chemical Registration)
    • Screening for photoinitiator migration per Swiss Ordinance (SR 817.023.21, Annex 10)

    Typical usage ratio

    • 1.2%–3.2% by weight of the intermediate stage; final photoinitiator ratio in resin typically 0.3%–1.0% depending on resin system

    Downstream process integration

    • Incorporated during synthesis of aryl morpholine-based photoinitiators via nitration and etherification steps, followed by purification prior to formulation into liquid and powder photoinitiators

    Final product types

    • UV curing photoinitiators for high-definition inkjet inks
    • UV-cured protective varnishes and overprint lacquers in packaging and electronics

    3. Intermediate for Liquid Crystal Material Synthesis

    Downstream producers select this compound for its stable aromatic morpholine structure, using it to synthesize advanced liquid crystal intermediates with tailored dielectric and optical properties required in high-contrast display technologies and specialty sensor assemblies.

    Industry compliance standards

    • IEC 61249 (Standard for halogen-free electronic materials)
    • ISO 14001 (Environmental Management for chemical manufacturers)
    • In-house FTIR and NMR analysis per custom LC material QC protocols

    Typical usage ratio

    • 0.8%–2.0% by molar ratio, adjusted in relation to the length and polarity target of the host LC mixture

    Downstream process integration

    • Used during the etherification and subsequent N-alkylation steps to form molecular cores in nematic and smectic LC mixtures; typically added after ring closure of precursor chains

    Final product types

    • Advanced nematic liquid crystal blends for TFT-LCD panels
    • Specialty LC materials for optical shutters and tunable filters

    4. Functional Dye Intermediate Production

    Specialty dye manufacturers use this compound as a critical building block during the synthesis of nitroaromatic dyes where precise electronic modification is necessary for targeted absorption maxima and colorfastness in technical textile and plastic applications.

    Industry compliance standards

    • OEKO-TEX® Standard 100 (Human-ecological safety in dye applications)
    • EN 71-3 (Safety of toys—migration of certain elements for use in colored plastics)
    • ISO 18314-1:2015 (Analytical color measurement in chemical substances)

    Typical usage ratio

    • Ranges from 0.4%–1.1% by batch weight; adjusted based on chromophore extension and depth of shade requirements

    Downstream process integration

    • Added during the condensation stage with reactive aromatic systems, typically following diazotization or alkylation reactions, to form extended pi-systems in functional dye molecules

    Final product types

    • Heat- and light-stable dyes for engineering polymers
    • High-brightness technical dyes for microelectronics and specialty fibers

    5. Advanced Agrochemical Intermediate Synthesis

    Chemical producers leverage this compound as a key structural element in the preparation of sophisticated nitro-morpholine herbicide and fungicide intermediates, where precise ethoxy substitution is engineered for bioactivity, selectivity, and environmental profile.

    Industry compliance standards

    • FAO/WHO Specification Guidelines for Agricultural Pesticides
    • ISO 14001: Environmental stewardship in synthesis
    • CFR Title 40 Part 180 (EPA tolerance in food crop chemicals, US market)

    Typical usage ratio

    • 0.9%–2.5% on a molar basis, tailored by end-customer’s crop and organism selectivity data

    Downstream process integration

    • Reacted during the heterocycle assembly phase, often entering after initial nitration and morpholine ring introduction; forms the scaffold for subsequent substitution or cyclization to active agrochemical ingredients

    Final product types

    • Nitro-aromatic herbicide intermediates for cereal and broadleaf crop protection
    • Morpholine-containing fungicide precursors for fruit and vegetable applications
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