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4-Methoxybenzoylacetonitrile

    • Product Name 4-Methoxybenzoylacetonitrile
    • Alias p-Anisoylacetonitrile
    • Einecs 209-995-0
    • 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

    493588

    Chemicalname 4-Methoxybenzoylacetonitrile
    Casnumber 553-84-4
    Molecularformula C10H9NO2
    Molecularweight 175.18
    Appearance White to off-white solid
    Meltingpoint 92-95°C
    Solubility Soluble in organic solvents like ethanol and acetone
    Purity Typically >98%
    Smiles COC1=CC=C(C=C1)C(=O)CC#N
    Inchi InChI=1S/C10H9NO2/c1-13-9-4-2-8(3-5-9)10(12)6-7-11/h2-5H,6H2,1H3
    Synonyms p-Anisoylacetonitrile; 4-Anisoylacetonitrile
    Storagetemperature Store at 2-8°C

    As an accredited 4-Methoxybenzoylacetonitrile factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing A 25-gram amber glass bottle with a secure screw cap, labeled "4-Methoxybenzoylacetonitrile, 25g, for laboratory use only."
    Shipping 4-Methoxybenzoylacetonitrile is shipped in tightly sealed, chemical-resistant containers to prevent moisture and contamination. The package is clearly labeled according to regulatory requirements and handled with care. It is transported under ambient conditions unless otherwise specified, ensuring compliance with safety guidelines for non-hazardous organic compounds.
    Storage 4-Methoxybenzoylacetonitrile should be stored in a tightly closed container in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizers. Protect it from moisture and direct sunlight. Keep the storage area clearly labeled and restrict access to trained personnel. Always follow applicable safety guidelines for handling and storage.
    Application of 4-Methoxybenzoylacetonitrile

    Applications of 4-Methoxybenzoylacetonitrile in Industrial Manufacturing

    4-Methoxybenzoylacetonitrile serves as a targeted building block in multiple high-value chemical manufacturing sectors. Its roles span fine chemical synthesis, pharmaceutical intermediates, agrochemical actives, dye precursors, organic electronic materials, and fragrance compound production. As the manufacturer, we supply this raw material directly to industrial downstream users who require consistent purity, traceability, and secure batch repeatability within complex formulations.

    1. Synthesis of Pharmaceutical Intermediates

    Our downstream partners in pharmaceutical manufacturing use 4-Methoxybenzoylacetonitrile as an advanced intermediate in the creation of key heterocyclic cores, including benzofuran and benzothiophene derivatives. Customers precisely engineer this compound into their multi-step active pharmaceutical ingredient (API) synthesis pipelines, requiring closely controlled conditions to avoid impurity carryover and ensure regulatory compliance for further medicinal chemistry transformations.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • Current Good Manufacturing Practice (cGMP), 21 CFR 210/211 (FDA)
    • European Pharmacopoeia (Ph. Eur.) relevant monographs and residual solvent limits
    • Controlled substance precursor documentation (where applicable)

    Typical usage ratio

    • 0.8–1.2 molar equivalents relative to the primary nucleophile or electrophile in stepwise synthesis; adjusted based on desired conversion rate and by-product management

    Downstream process integration

    • Charged as a key substrate during condensation or cyclization stages, typically under basic or Lewis acid catalysis; tight control of temperature and moisture necessary

    Final product types

    • Benzofuran-based API intermediates
    • Diarylamine precursors for CNS therapies
    • Pyridine ring synthons for oncology compounds

    2. Agrochemical Active Ingredient Synthesis

    Agrochemical manufacturers utilize 4-Methoxybenzoylacetonitrile to build active ingredient cores for new-generation herbicide and fungicide candidates. The nitrile and methoxy functionalities support cyclization and substitution chemistry crucial for field efficacy and environmental safety. Downstream formulation teams must maintain batch traceability for regulatory and stewardship audits related to active ingredient purity and environmental compliance.

    Industry compliance standards

    • FAO/WHO Specifications for Agricultural Pesticides
    • REACH (Registration, Evaluation, Authorisation and Restriction of Chemicals), EC 1907/2006
    • ISO 9001:2015 Quality Management System for supply chain traceability
    • Regulation (EC) No 1107/2009 for market placement of plant protection products

    Typical usage ratio

    • 0.5–2.5% w/w in concentrated active ingredient synthesis; ratio modulates according to targeted yield and process optimization studies

    Downstream process integration

    • Feeds into hydrocyanation, aromatic substitution, or ring-closing steps in agrochemical core assembly, supported by real-time analytical monitoring to avoid overreaction and impurity buildup

    Final product types

    • Triazole-based fungicide intermediates
    • Selective herbicide precursor molecules
    • Chemically defined safener seed treatment actives

    3. Aromatic Dye Intermediate Manufacturing

    Industrial dye houses and pigment makers employ 4-Methoxybenzoylacetonitrile as a pivotal intermediate in the synthesis of substituted anthraquinone and azo dye components. Its introduction enables controlled functionalization of the aromatic ring, facilitating chromophore development with high tinctorial strength and stability. Manufacturers demand batch reproducibility and ultra-low residual solvents to prevent downstream filtration problems and meet textile dyeing quality controls.

    Industry compliance standards

    • OEKO-TEX® STANDARD 100 Restricted Substances List for textile dyes
    • EN 71-3 Safety of Toys – migration of certain elements (relevant for dye coloring applications)
    • ZDHC MRSL (Zero Discharge of Hazardous Chemicals Manufacturing Restricted Substances List)
    • ISO 9001-certified process control for pigment production

    Typical usage ratio

    • 3–8% by mass in pre-condensation pigment paste preparations; precise dosing required for shade control and batch-to-batch consistency

    Downstream process integration

    • Serves as a primary nucleophilic component in acylation and coupling reactions, entering reactor trains after buffer and dispersant charging to maximize chromophore yield

    Final product types

    • Substituted anthraquinone dyes for PET textile fibers
    • Azo pigment intermediates for plastics coloration
    • High-performance printing inks

    4. Fine Fragrance and Aroma Compound Synthesis

    Specialty aroma compound manufacturers integrate 4-Methoxybenzoylacetonitrile into processes for complex fragrance intermediates, especially in the production of anisole and vanillin derivatives. Stringent odor purity and absence of process contaminants define acceptance for these applications, as fragrance end users require full traceability and allergen control to comply with downstream IFRA and cosmetic grade regulations.

    Industry compliance standards

    • IFRA (International Fragrance Association) Code of Practice
    • EU Regulation (EC) No 1223/2009 on cosmetic products
    • ISO 9001:2015 and FSSC 22000 for food-grade aroma manufacture
    • Allergen labelling per Regulation (EU) No 1169/2011

    Typical usage ratio

    • 0.1–1.5% by weight in complex aroma precursor synthesis; dosing fine-tuned based on the targeted aroma profile and residual solvent removal efficiency

    Downstream process integration

    • Added after aldehyde or acid precursor addition, entering reductive alkylation or condensation reactors at controlled pH and temperature for tailored aromatic profiles

    Final product types

    • Anisole-based fragrance ingredients
    • Vanillin derivative aroma compounds
    • Galaxolide analogues for home care

    5. Organic Electronic Material Synthesis

    The optoelectronics sector uses 4-Methoxybenzoylacetonitrile as a structural unit in the production of advanced organic semiconductors, OLED emissive layers, and hole-transport materials. Incorporating the nitrile motif enhances electronic conjugation and enables controlled energy level tuning, a critical aspect for device stability and performance. Production must observe zero metal contamination and full lot traceability to support reliability in large area electronic component fabrication.

    Industry compliance standards

    • RoHS Directive 2011/65/EU (Restriction of Hazardous Substances)
    • ISO 14001 Environmental Management System for electronics materials
    • JEDEC JESD625: Requirements for Handling Electrostatic–Discharge–Sensitive Devices
    • TSCA (Toxic Substances Control Act) inventory listing for specialty chemicals

    Typical usage ratio

    • 10–35 mol% as a monomer or comonomer feedstock in solution or vapor-phase polymerization; scaled by targeted film thickness and device application method

    Downstream process integration

    • Introduced into glovebox or dry room reactors for polymer precursor assembly, followed by precise purification to sub-ppm ionic and metallic impurities before device layer casting

    Final product types

    • OLED emitter layer precursor resins
    • Organic photovoltaic (OPV) active materials
    • Hole-transporting layer additives for thin film displays
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