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3-Acetyl-3-Methylpentanedicarbonitrile

    • Product Name 3-Acetyl-3-Methylpentanedicarbonitrile
    • Alias 3-Acetyl-3-methylglutaronitrile
    • Einecs 249-311-6
    • 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

    429782

    Iupac Name 3-acetyl-3-methylpentanedioic dinitrile
    Molecular Formula C9H12N2O
    Molecular Weight 164.21 g/mol
    Cas Number 37132-36-4
    Appearance White to off-white solid
    Melting Point 58-62°C
    Solubility Slightly soluble in water, soluble in organic solvents
    Density Approximately 1.06 g/cm³
    Purity Typically ≥98%
    Storage Conditions Store in a cool, dry place, tightly closed container

    As an accredited 3-Acetyl-3-Methylpentanedicarbonitrile factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The chemical `3-Acetyl-3-Methylpentanedicarbonitrile` is supplied in a 100-gram amber glass bottle, tightly sealed for safety.
    Shipping 3-Acetyl-3-Methylpentanedicarbonitrile is shipped in tightly sealed, chemical-resistant containers under cool, dry conditions. Packaging complies with regulatory standards for hazardous materials. Transport is handled by certified carriers with appropriate labeling and documentation, ensuring safety and integrity. Care is taken to avoid extreme temperatures, moisture, and physical damage during transit.
    Storage Store 3-Acetyl-3-Methylpentanedicarbonitrile in a tightly sealed container, in a cool, dry, and well-ventilated area away from direct sunlight and incompatible materials such as strong oxidizers. Protect from moisture and extreme temperatures. Clearly label storage containers and ensure proper ventilation in storage areas to avoid inhalation exposure. Follow standard chemical hygiene and safety procedures when handling and storing.
    Application of 3-Acetyl-3-Methylpentanedicarbonitrile

    Applications of 3-Acetyl-3-Methylpentanedicarbonitrile in Industrial Manufacturing

    Our expertise in advanced nitrile intermediates enables global manufacturers to achieve consistent quality in high-performance chemical synthesis. Below we detail the established industrial applications of 3-Acetyl-3-Methylpentanedicarbonitrile across specialized downstream sectors, with a focus on compliance, process integration, and final product types based on real-world use.

    1. Pharmaceutical Intermediate in Pyrimidine Synthesis

    Large-scale pharmaceutical companies utilize our material as a key building block for synthesizing heterocyclic compounds, particularly in the pyrimidine family. Our product’s dual nitrile functionality and reactivity enable efficient cyclization steps during the early phase of active pharmaceutical intermediate (API) production, supporting consistent batch yields and reproducible purity profiles. Downstream processes favor our raw material for constructing core chains in specific antiviral and anticancer drug candidates where regulatory traceability and contamination control are critical.

    Industry compliance standards

    • EU GMP Part II for APIs (EudraLex, Volume 4)
    • ICH Q7: Good Manufacturing Practices for Active Pharmaceutical Ingredients
    • US FDA 21 CFR Part 211: Current Good Manufacturing Practice for Finished Pharmaceuticals
    • Chinese Pharmacopoeia (ChP) process hygiene controls, as applicable by end-producer

    Typical usage ratio

    • 0.2–2.5 molar equivalents relative to core chain—precisely adjusted based on the desired heterocycle yield and downstream purification regime

    Downstream process integration

    • Added during the initial condensation or cyclization stage of heterocycle construction, often following protective group installation and preceding hydrogenation or oxidation steps

    Final product types

    • Pyrimidine-based APIs
    • Intermediates for nucleoside analogues
    • Precursors for antitumor agents
    • Pharmaceutical intermediates for targeted synthesis routes

    2. Agrochemical Precursor for Herbicide Synthesis

    Major agrochemical formulators apply our dicarbonitrile intermediate during the synthesis of complex pre-emergent herbicide molecules, where specific nitrile integration ensures molecular selectivity against broadleaf and grass weeds. Our product’s role as a strategic core fragment provides process flexibility and supports tight impurity control demanded by environmental authorities. Manufacturers rely on our consistent supply for large-volume campaigns, as purity directly affects downstream crystallization and granulation procedures required in pesticide active ingredient plants.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • European Regulation (EC) No 1107/2009 (placing plant protection products on the market)
    • ISO 9001:2015 (for quality system audits in contract synthesis)
    • REACH Registration, when supplied to EU-based producers

    Typical usage ratio

    • 10–20% by weight of total precursor mass, with the exact proportion set by targeted herbicide backbone requirements and batch scale

    Downstream process integration

    • Charged into the condensation reaction vessel during initial chain assembly, followed by chlorination or alkylation prior to formulation into technical concentrate

    Final product types

    • S-triazine herbicides (e.g., simazine precursors)
    • Pyridine- and pyrimidine-based herbicidal actives
    • Technical grade crop protection active ingredients
    • Granular and suspensible concentrate formulations

    3. Fine Chemical Intermediate for Dye & Pigment Manufacture

    Our nitrile compound serves as a tailored intermediate for dye and pigment synthetic routes, where the acetyl-methyl substitution pattern facilitates subsequent oxidation, condensation, or cyclization reactions leading to high-value azo and heterocycle-based chromophores. Precision in molecular addition and side-chain control during integration delivers the color fastness, intensity, and stability demanded by textile and plastics industries. Batch-to-batch traceability enables trace impurity management in accordance with export quality audits.

    Industry compliance standards

    • OEKO-TEX® Standard 100 (input list for textile coloration)
    • ISO 9001:2015 (fine chemical manufacturing)
    • REACH Annex XVII compliance for pigments exported to the EU
    • China National GB Standards for dye and pigment input materials

    Typical usage ratio

    • 3–8% by weight of dye intermediate batch; ratio set by chromophore type and final hue/fastness properties targeted

    Downstream process integration

    • Integrated during the primary coupling reaction or in the nucleophilic addition step forming the base chromophore, preceding sulfonation or granulation

    Final product types

    • Mono- and di-azo dyes
    • Polycyclic aromatic pigments
    • Reactive dye intermediates for cotton and polyester coloration
    • Specialty pigments for plastics and coatings

    4. Intermediate for API Fine Chemical Custom Synthesis (CMO/Custom Manufacturing)

    Custom manufacturing organizations (CMOs) and in-house API divisions use our compound for contract synthesis projects requiring complex carbon–nitrogen assembly steps. Our consistent quality and validated trace impurity profile support process validation documentation and meet customer-specific route requirements during new chemical entity (NCE) synthesis. This role frequently involves multi-step transformations where side-chain control from our intermediate is essential in assembling scaffold structures under stringent regulatory conditions.

    Industry compliance standards

    • ISO 13485:2016 for medical device-linked contract chemicals
    • ICH Q11: Development and Manufacture of Drug Substances
    • GMP for APIs (as per customer contract region)
    • Custom QC protocols defined in Confidential Disclosure Agreements (CDA, CMO)

    Typical usage ratio

    • Variable: 5–40% by mol in pathway-specific step, configured according to customer-supplied route and target yield

    Downstream process integration

    • Fed into the key carbonylation, cyanation, or condensation stage of NCE assembly, with downstream work-up by preparative chromatography or crystallization for purity requirement

    Final product types

    • Complex pharmaceutical intermediates
    • Building blocks for clinical stage API candidates
    • Reference standards and analytical markers
    • Chemical intermediates for fine chemical catalogs

    5. Precursor in Specialty Polymer Modifier Synthesis

    Leading specialty polymer producers rely on our dicarbonitrile intermediate to introduce pendant nitrile and ketone functionalities into polymer backbones. The unique structure enables grafting reactions that modulate glass transition temperature, enhance barrier properties, and create reactive sites for further chemical modification. Our material’s defined molecular weight and low polyisomeric impurity content ensure predictable results in specialty copolymer modifier production utilized in high-performance adhesives and protective coatings.

    Industry compliance standards

    • ISO 9001:2015 (polymer chemical quality assurance)
    • EN 14021:2016 for environmental labeling relevant to polymer additives
    • RoHS 2011/65/EU (where modifier is used in electronics-sensitive applications)
    • CFR Title 21, Sections 175–177 (for specialty polymers in indirect food contact, by application)

    Typical usage ratio

    • 0.5–3.0% by weight, with loading selected to balance mechanical property modification against base polymer processability

    Downstream process integration

    • Introduced in the co-polymerization or post-polymer backbone modification step, followed by melt blending or solution processing depending on target application

    Final product types

    • Polymer chain-end modifiers
    • Adhesive and coating auxiliaries
    • Nitrile-functionalized specialty elastomers
    • Reactive copolymers for electronics and barrier films
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