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N-Ethyl-N-Methoxycarbonylethyl Aniline

    • Product Name N-Ethyl-N-Methoxycarbonylethyl Aniline
    • Alias EMCA
    • Einecs '410-090-6'
    • 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
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    Specifications

    HS Code

    844296

    Chemical Name N-Ethyl-N-Methoxycarbonylethyl Aniline
    Molecular Formula C13H19NO3
    Molecular Weight 237.30 g/mol
    Appearance Colorless to pale yellow liquid
    Boiling Point Approx. 340°C
    Density 1.08 g/cm3
    Solubility Slightly soluble in water, soluble in organic solvents
    Purity Typically >98%
    Cas Number 70973-78-5
    Smiles CCN(Cc1ccccc1)CC(=O)OC
    Storage Conditions Store in a cool, dry, well-ventilated place

    As an accredited N-Ethyl-N-Methoxycarbonylethyl Aniline factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 500g amber glass bottle with secure screw cap; labeled with chemical name, formula, hazard symbols, and handling/storage instructions.
    Shipping N-Ethyl-N-Methoxycarbonylethyl Aniline should be shipped in tightly sealed containers, protected from moisture and direct sunlight. Comply with all relevant chemical transportation regulations. Label as a laboratory chemical, handle with appropriate hazard warnings, and provide documentation such as Safety Data Sheets. Store in a cool, dry, and well-ventilated area during transit.
    Storage Store **N-Ethyl-N-Methoxycarbonylethyl Aniline** in a tightly closed container in a cool, dry, and well-ventilated area. Protect it from moisture, heat, and direct sunlight. Keep away from oxidizing agents and sources of ignition. Use chemical-resistant containers and ensure proper labeling. Follow standard laboratory safety protocols and store in accordance with local regulations for hazardous chemicals.
    Application of N-Ethyl-N-Methoxycarbonylethyl Aniline

    Applications of N-Ethyl-N-Methoxycarbonylethyl Aniline in Industrial Manufacturing

    N-Ethyl-N-Methoxycarbonylethyl Aniline is a specialized intermediate designed for narrowly focused downstream chemical synthesis. As direct manufacturers, we collaborate closely with end-producers in high-value sectors that demand precise compliance, repeatable formulation, and deeply integrated process steps. The following applications illustrate how this intermediate contributes to downstream innovation, efficiency, and regulatory conformance across exacting use cases.

    1. Synthesis of High-Purity Fluorescent Dyes for Security Printing

    Specialty fluorescent dyes play a critical role in the production of anti-counterfeiting inks used in currency, official documents, and brand protection labels. Our intermediate is introduced as a key aromatic amine within the dye synthesis step, directly affecting chromophore integrity and emission wavelength specificity. Strict traceability and batch uniformity are demanded throughout the production cycle to meet both international and national legal standards governing security ink applications.

    Industry compliance standards

    • CEN/TS 16724:2014 (Security inks for authentication in documents)
    • ISO/IEC 17025:2017 (Laboratory QC requirements for dye analysis)
    • EN 71-3:2019 (Migration of certain elements in toy and writing inks)
    • Customs and currency ink standards (Federal Reserve, ECB)

    Typical usage ratio

    • 0.2–1.0 wt% in bulk dye synthesis; further adjusted based on emission intensity and ink matrix compatibility

    Downstream process integration

    • Added during the aromatic amination stage of fluorescent dye manufacturing, before halogenation or metal complexation steps
    • Undergoes purification and QC assay before downstream dispersion in carrier ink systems

    Final product types

    • Security inks for banknotes
    • Fluorescent overprint varnishes for passports and identification cards
    • Covert and overt brand protection inks

    2. API Intermediate for Selective Serotonin Receptor Ligand Synthesis

    Pharmaceutical companies incorporate this intermediate in the multi-step synthesis of certain serotonin receptor modulators. Its unique structure enables substitution reactions, optimizing yield and facilitating downstream chiral separations. Full documentation and GMP-aligned sourcing are required, as trace residuals and process-related impurities may affect pharmacological validation and regulatory submission.

    Industry compliance standards

    • ICH Q7 (Good Manufacturing Practice for Active Pharmaceutical Ingredients)
    • EU GMP Part II for APIs
    • US FDA 21 CFR Part 210/211 (Pharmaceutical Manufacturing)
    • EP, USP, JP monographs (route-dependent)

    Typical usage ratio

    • 0.5–1.5 equivalents per target API molecule (stoichiometric adjustment per synthesis route and desired regioselectivity)

    Downstream process integration

    • Engaged during the key N-ethylation or N-alkylation step of indole- or quinoline-based pharmaceutical intermediate synthesis
    • Subjected to rigorous in-process control (IPC) to monitor residual solvents and genotoxic impurities

    Final product types

    • Serotonin receptor agonists for CNS therapeutics
    • Precursor compounds for neuropsychiatric drug development
    • Pharmaceutical grade fine chemicals for clinical and pilot-scale trials

    3. Resin Modification Agent in Advanced Epoxy System Formulation

    The addition of this aromatic amine derivative to specialty epoxy resins modifies cross-linking density and end-use thermal stability, enabling enhanced performance for electronics encapsulation and PCB coatings. Industrial users require transparent supply chain provenance and batch analytics to meet strict electrical and mechanical standards, as even minor compositional variance impacts long-term device reliability.

    Industry compliance standards

    • IPC-4101 (Base materials for printed boards)
    • UL 94 V-0 (Flame retardancy for polymeric materials)
    • REACH Annex XVII (Aromatic amine restriction, SVHC review)
    • RoHS Directive 2011/65/EU (Lead, mercury, and amine compound thresholds in electronics)

    Typical usage ratio

    • 0.3–1.2 phr (parts per hundred resin) during epoxy premixing; rate adjusted according to required glass transition temperature (Tg) and cure profile

    Downstream process integration

    • Premixed into the base resin prior to solvent evaporation and pre-polymerization
    • Enters main reactor under inert atmosphere; undergoes cure protocol in conjunction with hardeners and accelerators

    Final product types

    • High-performance dry film photoresists
    • Microelectronic encapsulants for semiconductor packaging
    • Conformal coatings for multilayer PCBs

    4. Intermediate for Specialty Agrochemical Synthesis (Plant Growth Regulators)

    This amine derivative serves as a building block in the synthesis of highly targeted plant growth regulators, specifically auxin or cytokinin analogues. Agrochemical formulators prioritize raw materials with precisely controlled impurity profiles, as trace contaminants can affect crop-response field trials and regulatory submissions for pesticide approval.

    Industry compliance standards

    • FAO/WHO Specification for Plant Growth Regulators
    • OECD Guidelines for the Testing of Chemicals (Residue analysis, toxicology)
    • ISO 17034:2016 (Reference material producer requirements)
    • ECHA Guidance on Plant Protection Products (EU Regulation EC 1107/2009)

    Typical usage ratio

    • 0.1–0.7 molar ratio relative to active agrochemical core scaffold, fine-tuned based on desired plant-biological activity in formulation trials

    Downstream process integration

    • Added during condensation or amidation step of plant regulator molecule synthesis
    • QC sampling after each batch to verify absence of toxic aromatic amine byproducts and compliance with Maximum Residue Levels (MRLs)

    Final product types

    • Commercial foliar sprays for cereal and oilseed crops
    • Seed coating agents for controlled germination
    • Root enhancer formulations for horticulture

    5. Intermediate for Organic Pigment Manufacturing (High-Purity Yellow and Red Dyes)

    Producers of high-value organic pigments for industrial coatings and plastics leverage this intermediate in controlled diazo coupling reactions. This produces colorants with tightly regulated hue, particle size, and solvent resistance, particularly for automotive and architectural finishes. Quality-critical sectors require not only a narrow impurity profile, but also delivery under documented process controls to meet end-use safety and regulatory disclosure requirements.

    Industry compliance standards

    • EU Regulation (EC) No 1907/2006 (REACH) for colorants
    • ISO 787-24:1985 (General methods of test for pigments and extenders)
    • ASTM D3721 (Color stability and migration testing)
    • Automotive OEM specification release standards

    Typical usage ratio

    • 0.5–2.0 wt% in pigment synthesis step; range set by required color intensity and substrate compatibility

    Downstream process integration

    • Employed in diazotization or azo coupling stage of organic pigment production
    • Introduced prior to filtration, milling, and particle size adjustment

    Final product types

    • Organic pigment powders for high-solid coatings
    • Color masterbatches for polyolefin extrusion
    • Automotive basecoat and topcoat pigment dispersions

    6. Photoinitiator Precursor in UV-Cured Coating Formulation

    Manufacturers of UV-cured coatings formulate novel photoinitiators using this raw material for its high absorption coefficient and reactive aromatic structure. By integrating this molecule during the custom synthesis of type I and II photoinitiators, coating producers achieve faster cure times and greater film integrity, particularly for high-throughput automated production environments in electronics, wood, and optical lenses.

    Industry compliance standards

    • ISO 9001:2015 (Quality management for chemical synthesis)
    • GB/T 23987-2009 (UV-curing coatings quality standard in Asia-Pacific)
    • DIN EN 71-3:2019 (Coating material standards for toys and contact surfaces)
    • California Prop 65 (Reporting for photoinitiator ingredients)

    Typical usage ratio

    • Typically 0.4–1.0 phr based on the target photoinitiator yield and UV absorption specifications for the coating matrix

    Downstream process integration

    • Synthesized into benzoin ether or acetophenone-type photoinitiators via controlled alkylation
    • Final photoinitiator then blended into UV-curable resin formulations before application and curing

    Final product types

    • UV-cured clear coatings for smartphone and tablet cases
    • High-gloss finishes for engineered wood flooring
    • Photo-reactive coatings used in lens and display manufacturing
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