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N-[3-[(2-Cyanoethyl)Amino]-4-Methoxyphenyl]Acetamide

    • Product Name N-[3-[(2-Cyanoethyl)Amino]-4-Methoxyphenyl]Acetamide
    • Alias STK160830
    • Einecs 629-444-6
    • 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

    706738

    Iupac Name N-[3-[(2-cyanoethyl)amino]-4-methoxyphenyl]acetamide
    Cas Number 83274-74-8
    Molecular Formula C12H15N3O2
    Molecular Weight 233.27 g/mol
    Appearance Off-white to yellowish solid
    Melting Point 97-101 °C
    Solubility Soluble in DMSO, slightly soluble in water
    Storage Temperature 2-8 °C
    Purity Typically ≥98%
    Smiles CC(=O)NC1=CC(=C(C=C1)NCC#N)OC
    Inchi InChI=1S/C12H15N3O2/c1-9(16)15-11-5-4-10(6-12(11)17-2)14-8-3-7-13/h4-6,14H,3,8H2,1-2H3,(H,15,16)
    Synonyms 3-[(2-Cyanoethyl)amino]-4-methoxyacetanilide

    As an accredited N-[3-[(2-Cyanoethyl)Amino]-4-Methoxyphenyl]Acetamide 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 25 grams of N-[3-[(2-Cyanoethyl)Amino]-4-Methoxyphenyl]Acetamide, labeled with safety and chemical information.
    Shipping This chemical, N-[3-[(2-Cyanoethyl)Amino]-4-Methoxyphenyl]Acetamide, should be shipped in a tightly sealed container, protected from light, moisture, and incompatible substances. Transport must comply with local, national, and international regulations for chemicals, including appropriate labeling and documentation. Use secondary containment and consult the Safety Data Sheet (SDS) for detailed handling instructions.
    Storage N-[3-[(2-Cyanoethyl)Amino]-4-Methoxyphenyl]Acetamide should be stored in a tightly sealed container, protected from light, moisture, and incompatible substances, at a cool and dry location, typically at 2–8°C (refrigerator) unless otherwise specified. Avoid exposure to strong oxidizers and acids. Ensure proper labeling and access only to trained personnel. Handle under well-ventilated conditions with appropriate personal protective equipment.
    Application of N-[3-[(2-Cyanoethyl)Amino]-4-Methoxyphenyl]Acetamide

    Applications of N-[3-[(2-Cyanoethyl)Amino]-4-Methoxyphenyl]Acetamide in Industrial Manufacturing

    As a direct manufacturer, we supply N-[3-[(2-Cyanoethyl)Amino]-4-Methoxyphenyl]Acetamide to leading industrial sectors. This intermediate plays a critical role in high-value synthesis across pharmaceuticals, advanced agricultural inputs, specialty pigments, and electronic materials. Below, we detail four key downstream applications with a focus on compliance, formulation, integration, and end-product scope.

    1. Pharmaceutical Intermediate for Active Ingredient Synthesis

    Pharmaceutical manufacturers use N-[3-[(2-Cyanoethyl)Amino]-4-Methoxyphenyl]Acetamide as a key intermediate in synthetic routes towards certain APIs (active pharmaceutical ingredients). Its molecular structure allows selective introduction of cyanoethyl or methoxy substitutions, which are essential in synthesizing small-molecule therapeutics, particularly in oncology and neurology research. Our customers utilize tailored protocols to meet rigorous regulatory requirements, ensuring batch traceability and impurity control from our starting material.

    Industry compliance standards

    • ICH Q7 GMP for Active Pharmaceutical Ingredients
    • US FDA 21 CFR Part 211 for Finished Pharmaceuticals
    • EU EMA EudraLex Volume 4
    • USP/NF and EP monographs for related substances

    Typical usage ratio

    • Used between 10-25% molar equivalents in stepwise API syntheses, based on proprietary pathway requirements. Adjustments depend on yield optimization and impurity thresholds defined by process validation.

    Downstream process integration

    • Charged at the amidation or nucleophilic addition stage of multi-step organic synthesis, prior to final condensation and purification of the target active ingredient.

    Final product types

    • Anti-cancer drug intermediates
    • CNS pharmaceutical APIs
    • Fine chemical fragments for combinatorial drug development
    • Pharmaceutical research standards

    2. Synthesis of High-Performance Agrochemical Compounds

    Formulators of advanced crop protection agents employ this compound as a unique building block for herbicide and pesticide molecules. The presence of the cyanoethyl group contributes to bioactivity, while the methoxy substitution improves solubility and plant uptake properties. Agricultural input manufacturers integrate our material into multi-step reactions under controlled environments, supported by robust documentation for global agrochemical registrations.

    Industry compliance standards

    • OECD Principles of Good Laboratory Practice (GLP)
    • FAO/WHO Joint Meeting on Pesticide Specifications (JMPS) guidelines
    • EPA FIFRA compliance for US market
    • REACH Regulation (EC) No 1907/2006 for EU

    Typical usage ratio

    • Incorporated typically at 5-12% w/w relative to total raw input mass in pre-formulation stages. Exact proportion varies according to active ingredient type and target spectrum, with pilot batches confirming optimum efficacy-to-toxicity ratio.

    Downstream process integration

    • Added during the initial condensation or substitution reaction in synthesis of target pesticide, followed by isolation and downstream granulation, milling, or EC (emulsifiable concentrate) formulation.

    Final product types

    • Systemic herbicide technical concentrates
    • Active ingredient precursors for post-emergent crop protection
    • Pre-mix granules for rice, wheat, or corn fields
    • Benchmark substances for field trial studies

    3. Precursor for Specialty Pigments in Electronic Displays

    In the specialty pigment industry, this chemical acts as a tailored intermediate for synthesizing molecular dyes applied in OLED and high-resolution display manufacturing. Its electron-donating methoxy group and cyanoethyl functionality are valued for influencing pigment stability, color purity, and charge transport characteristics. Customers apply strict cleanliness and traceability controls from procurement through final pigment integration to meet display industry standards.

    Industry compliance standards

    • RoHS Directive 2011/65/EU for restriction of hazardous substances
    • IEC 61249-2-21 for halogen-free requirements in electronics
    • ISO 9001:2015 certified pigment production
    • JEITA guidelines for advanced electronic materials

    Typical usage ratio

    • Utilized at 3-9% w/w of the final pigment mass, with exact quantity tailored to achieve target chromaticity and thermal resistance required by display OEMs.

    Downstream process integration

    • Reacted in the core step of chromophore backbone construction, followed by purification and deposition onto polymeric or glass substrates as part of dye incorporation.

    Final product types

    • Red and green OLED dyes
    • Specialty photoreactive pigments for TFT-LCD panels
    • Printable color filter dispersions
    • Laser addressable colorants for advanced optic devices

    4. Advanced Intermediate in Electronic Chemical Manufacturing

    Fabricators of semiconductors and advanced printed circuit materials use this molecule to build organic electronic compounds, including sophisticated photoresists and dielectric polymers. The dual functional groups confer controllable etching and pattern-transfer properties, providing reliable performance for micro-patterning at sub-micron resolutions. Customers rely on precise input specifications from our production for robust batch-to-batch reproducibility and integration with automated dispensing systems.

    Industry compliance standards

    • SEMI Standards for electronic material purity (SEMI C88, C98)
    • IEC 62474 for material declaration in the electrical/electronic sector
    • ISO 14001:2015 for environmental management in chemical production
    • SIA (Semiconductor Industry Association) Green Chemistry recommendations

    Typical usage ratio

    • Dosed at 2-6% by weight into electronic chemical formulations, with fine adjustments made per wafer substrate type and pattern feature size.

    Downstream process integration

    • Incorporated into precursor baths or spin-coating solutions for photoresist, dielectric, or organic conductor layer development prior to UV-lithography and etching steps.

    Final product types

    • Photoresist resin intermediates
    • Organic dielectric films for integrated circuits
    • Low-κ insulating coatings for microchip production
    • Printed circuit board substrates
    Free Quote

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