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4-Methylbenzoylacetonitrile

    • Product Name 4-Methylbenzoylacetonitrile
    • Alias p-Toluylacetonitrile
    • Einecs 217-444-5
    • 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

    533263

    Cas Number 5745-88-0
    Molecular Formula C10H9NO
    Molecular Weight 159.19 g/mol
    Iupac Name 2-(4-methylbenzoyl)acetonitrile
    Appearance White to off-white crystalline powder
    Melting Point 83-85 °C
    Boiling Point 352.7 °C at 760 mmHg
    Density 1.12 g/cm³
    Solubility Slightly soluble in water; soluble in organic solvents like ethanol and acetone
    Purity Typically ≥98%
    Refractive Index 1.560 (estimate)
    Flash Point 167.1 °C

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

    Packing & Storage
    Packing 250g of 4-Methylbenzoylacetonitrile is supplied in a sealed amber glass bottle with a secure screw cap and warning label.
    Shipping 4-Methylbenzoylacetonitrile is typically shipped in tightly sealed containers, compliant with relevant chemical transportation regulations. It should be stored in a cool, dry, and ventilated area, away from incompatible substances. Proper labelling and documentation are required, and protective measures must be taken to prevent leaks or spills during transit.
    Storage Store 4-Methylbenzoylacetonitrile in a cool, dry, and well-ventilated area, away from direct sunlight, heat sources, and incompatible substances such as strong oxidizers. Keep the container tightly closed and clearly labeled. Use corrosive- and solvent-resistant containers, and avoid moisture exposure. Ensure access to emergency spill cleanup materials and follow all local regulations for hazardous chemical storage.
    Application of 4-Methylbenzoylacetonitrile

    Applications of 4-Methylbenzoylacetonitrile in Industrial Manufacturing

    4-Methylbenzoylacetonitrile serves as a key intermediate in specialized chemical synthesis within the pharmaceutical, agrochemical, and fine chemical industries. As a trusted raw material manufacturer, we support downstream partners with product consistency and formulation insight, enabling controlled scale-up across regulated fields. Below we outline application scenarios with their compliance foundation, recommended usage ratios, integration within established processing steps, and examples of typical end-products.

    1. Pharmaceutical Intermediates for Active Pharmaceutical Ingredient (API) Synthesis

    Pharmaceutical manufacturers utilize 4-Methylbenzoylacetonitrile in constructing advanced intermediates for APIs, particularly within heterocyclic and aromatic scaffold production. The compound fits into step-growth syntheses where precise chemical transformations are performed under GMP-compliant conditions. Our QC systems and technical support ensure consistent supply meeting documentation and traceability requirements for DMF submissions and regulatory filings.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • European Pharmacopoeia monographs (as applicable for downstream APIs)
    • US FDA 21 CFR Parts 210/211 for drug substance manufacturing
    • WHO GMP Guidelines for Pharmaceutical Production

    Typical usage ratio

    • Application concentrations range between 0.2 molar equivalents to 1.0 molar equivalents in the condensation or cyclization steps, depending on the complexity of the target API framework. Process chemists determine the exact ratio by lab-scale yield optimization and impurity profile requirements for validation batches.

    Downstream process integration

    • Added during the initial condensation or cyclization phase in multi-stage synthesis of nitrogen-containing or aromatic heterocyclic APIs; followed by subsequent derivatization, isolation, and purification steps under controlled environmental parameters.

    Final product types

    • Antiviral drug intermediates
    • Non-steroidal anti-inflammatory intermediates
    • Cancer therapeutic scaffolds
    • CNS-active compound precursors

    2. Agrochemical Intermediate for Herbicide and Fungicide Synthesis

    Downstream agrochemical companies incorporate this compound as a backbone-building block for selective herbicides and systemic fungicides. Its chemical reactivity enables formation of substituted aromatic and cyano structures, essential to modern crop protection products. Our supply supports full-lot traceability, compliance with environmental and worker protection criteria, and integration with existing automation in plant-scale synthesis.

    Industry compliance standards

    • ISO 9001:2015 for Quality Management in Chemical Plants
    • REACH Regulation (EC) No 1907/2006 (substance registration, evaluation, and authorization)
    • FAO/WHO Specifications for Plant Protection Products
    • Globally Harmonized System (GHS) of Classification and Labelling of Chemicals

    Typical usage ratio

    • Added at 0.5–2.5% of the total batch weight, adjustable based on active ingredient synthesis route and yield optimization studies. Formulators may slightly increase ratio to account for stoichiometric requirements in multi-component couplings and sidechain extensions.

    Downstream process integration

    • Charged in the key coupling or chain-elongation stage, typically under anhydrous or controlled-temperature conditions, prior to hydrolysis or esterification. Subsequent processes may involve distillation, crystallization, and micronization for active ingredient isolation.

    Final product types

    • Triazole herbicides
    • Aromatic cyanide-based fungicides
    • Precursor mixtures for post-emergent weed control agents
    • Downstream ester and amide derivatives for foliar sprays

    3. Fine Chemical Synthesis for Dyes and Pigment Intermediates

    Manufacturers of specialty dyes leverage the reactivity of the material for constructing azo, heterocyclic, or cyano-linked chromophores. This application requires rigorous color purity and stability, with synthesis occurring under closely monitored batch conditions. End users expect reliable supply chains compliant with industrial safety and product registration for consumer and industrial pigment applications.

    Industry compliance standards

    • ISO 14001:2015 Environmental Management Systems for Chemical Production
    • OEKO-TEX® Standard 100 (where applicable for textile-related end products)
    • EN 71 Part 3: Safety of Toys—Migration of Certain Elements (for pigment in children's products)
    • REACH Annex XVII—Restrictions on the manufacture, placing on market and use of certain dangerous substances

    Typical usage ratio

    • Employed at 0.8–3.0% based on pigment or dye batch mass, with specific proportion determined by the chromophore system and desired color intensity. Process engineers refine ratios in pilot batches to secure color reproducibility and avoid undertones or impurities.

    Downstream process integration

    • Injected in the precursor formation stage during diazotization, coupling, or condensation steps; may be followed by filtration, washing, and drying processes to obtain dye intermediates further processed into pigments, dispersions, or concentrates.

    Final product types

    • Anthraquinone and azo dye intermediates
    • Specialty pigment dispersions for coatings and inks
    • Synthetic textile colorants
    • High-stability colorant bases for plastics

    4. High-Performance Chemical Building Blocks for Organic Electronic Materials

    Producers of organic semiconducting materials rely on this intermediate for constructing nitrogen- or cyano-functionalized aromatic modules integral to OLED displays and advanced sensor devices. Our product integrates within custom organic synthesis routes meeting precise electronic and purity thresholds and addresses regulatory needs in markets with advanced technical barriers and restrictions on restricted substances.

    Industry compliance standards

    • RoHS Directive 2011/65/EU (Restriction of Hazardous Substances in Electrical and Electronic Equipment)
    • IEC 62474 Material Declaration for Products of and for the Electrotechnical Industry
    • ISO 9001:2015 for process and quality management in electronics chemicals
    • REACH Regulation SVHC compliance (as relevant to substance handling)

    Typical usage ratio

    • Utilized at 0.5–1.5% within precursor monomer or oligomer synthesis, adjusted based on chain length and target device performance. Developers define the final ratio dependent on testing for charge transport and thermal stability in optoelectronic applications.

    Downstream process integration

    • Introduced during targeted cross-coupling or nucleophilic substitution reactions, before polymerization or vacuum sublimation; purity is maintained to minimize signal loss and optimize device lifespan. Final compounds undergo purification and casting for subsequent device fabrication.

    Final product types

    • OLED and PLED emission layers
    • Organic solar cell sensitizing dyes
    • Electronic sensor substrates
    • Charge-transport materials for thin-film transistors
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