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3-Acetyl-2,4-Dimethyl-5-Carbethoxypyrrole

    • Product Name 3-Acetyl-2,4-Dimethyl-5-Carbethoxypyrrole
    • Alias ethyl 3-acetyl-2,4-dimethyl-1H-pyrrole-5-carboxylate
    • Einecs 249-971-6
    • 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

    721427

    Chemicalname 3-Acetyl-2,4-Dimethyl-5-Carbethoxypyrrole
    Casnumber 38294-77-4
    Molecularformula C11H15NO3
    Molecularweight 209.24
    Appearance Yellowish oil
    Boilingpoint 315.4 °C at 760 mmHg
    Density 1.106 g/cm3
    Solubility Soluble in organic solvents
    Purity Typically >98%
    Refractiveindex 1.515
    Storagetemperature Store at 2-8 °C
    Smiles CC1=NC(=C(C(=C1C)C(=O)OCC)C(=O)C)C
    Inchi InChI=1S/C11H15NO3/c1-5-9(13)7-8(3)12-10(4)11(7)14-6-2/h5H,6H2,1-4H3

    As an accredited 3-Acetyl-2,4-Dimethyl-5-Carbethoxypyrrole 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, sealed with a screw cap, labeled with chemical name, CAS number, and hazard information.
    Shipping 3-Acetyl-2,4-Dimethyl-5-Carbethoxypyrrole should be shipped in tightly sealed containers, away from heat, moisture, and incompatible substances. Package within appropriate chemical-resistant secondary containment. Label containers clearly as per regulatory guidelines. Handle with care and ship following all relevant local, national, and international hazardous material transport regulations, including documentation and emergency procedures.
    Storage Store 3-Acetyl-2,4-Dimethyl-5-Carbethoxypyrrole in a tightly sealed container, protected from light and moisture, in a cool, dry, and well-ventilated area. Keep away from strong oxidizing agents and sources of ignition. Clearly label the container, and handle under fume hood if possible. Follow standard chemical storage protocols and consult the Safety Data Sheet for specific guidance.
    Application of 3-Acetyl-2,4-Dimethyl-5-Carbethoxypyrrole

    Applications of 3-Acetyl-2,4-Dimethyl-5-Carbethoxypyrrole in Industrial Manufacturing

    Our expertise in pyrrole chemistry supports key value chains where 3-Acetyl-2,4-Dimethyl-5-Carbethoxypyrrole provides specific structural benefits for downstream manufacturers. Below we detail its industrial uses, covering regulated sectors and defining its role in advanced formulation and processing.

    1. Pharmaceutical Intermediates for Heterocyclic Drug Synthesis

    This pyrrole derivative acts as an intermediate in the manufacture of complex heterocyclic scaffolds widely used in novel drug candidates. Pharmaceutical firms incorporate it during multi-step synthesis of pyrrole-fused APIs and pharma actives. Direct coupling, condensation, and cyclization reactions use this building block to create bioactive structures with improved pharmacokinetics. Careful batch tracking and documentation remain essential from raw material input to purified product.

    Industry compliance standards

    • ICH Q7 GMP for API manufacturing
    • US FDA 21 CFR Part 211
    • EU EudraLex Volume 4
    • USP/NF and Ph. Eur. monograph reference standards (where applicable in downstream API)

    Typical usage ratio

    • 0.5–3.5 molar equivalents in condensation steps, adjusted per target compound yield and impurity profile

    Downstream process integration

    • Added as a key functionalized pyrrole moiety at intermediate assembly stage in multiphase batch synthesis

    Final product types

    • Pyrrole-based drug substances (APIs)
    • Intermediates for oncology, CNS, or anti-infective agents
    • Pharmaceutical reference standards

    2. Advanced Pigment and Dye Additive Manufacture

    In colorant production, this compound introduces unique electronic properties that influence hue, stability, and light fastness of specialty dyes and pigments. Formulators utilize it to achieve targeted shades in high-performance inks, plastics, and coatings. Integration takes place during the aromatic π-conjugation or pigment core extension step, balancing solubility and dispersion in final systems.

    Industry compliance standards

    • EN 71-3: Migration of certain elements for toy safety (pigments in toys)
    • REACH Annex XVII, item 43 (azo compounds in consumer goods)
    • DIN 55990-1 (requirements for organic colorants in coatings)
    • CFR Title 21, Sections 74–82 (US FDA for food-contact uses)

    Typical usage ratio

    • 0.8–2.2 wt% relative to batch pigment mass, raised or reduced depending on tinting strength

    Downstream process integration

    • Reacted at dye core ring-modification phase, often followed by sulfonation or metallization (if required by pigment type)

    Final product types

    • Organic pigments for plastics and paints
    • Solvent-based printing dyes
    • Specialty textile colorants
    • Food-grade color additives

    3. Aroma and Flavor Ingredient Synthesis

    This pyrrole ester finds utility in the synthesis of savory aroma compounds and processed food flavor enhancers. Its subtle alkyl and carbonyl profile contributes to roasted, nutty, or brothy aroma top-notes. Food chemists apply it as a precursor in Maillard-related flavor molecule pathways, through controlled cyclization, hydrolysis, or condensation with sugars and peptides, monitored by GC-MS analysis for purity and compliance.

    Industry compliance standards

    • FAO/WHO JECFA food additive evaluation (for flavoring purposes)
    • US FDA 21 CFR Part 172.515 “Synthetic flavoring substances and adjuvants”
    • EU Regulation (EC) No 1334/2008 (flavorings and certain food ingredients with flavoring properties)
    • ISO 22000 food safety management

    Typical usage ratio

    • 0.02–0.1 wt% in compounded food flavor bases, assayed based on sensory threshold and target profile

    Downstream process integration

    • Charged into flask during aroma precursor synthesis phase or direct functional group transformation in flavor compounding lines

    Final product types

    • Savory flavor mixtures for snacks and ready meals
    • Specialty aroma blends for sauces or seasonings
    • Reaction flavors for industrial food manufacturers

    4. Organic Electronic Material Precursors

    Manufacturers use this pyrrole variant as a functional intermediate in the production of heterocyclic monomers destined for conductive polymers and organic semiconductors. Specialty electronics firms employ it during Suzuki or Stille coupling to construct advanced bandgap materials. Strict process control and contaminant management are essential due to sensitivity in electronic-grade applications.

    Industry compliance standards

    • IEC 60194 for electronic component materials
    • RoHS Directive 2011/65/EU (control of hazardous substances in electrical/electronic equipment)
    • IPC-1752 material declaration requirements
    • ISO 9001:2015 (for quality management in component manufacture)

    Typical usage ratio

    • 0.5–1.5 molar equivalents per monomer batch, adjusted by desired electronic mobility and polymer chain length

    Downstream process integration

    • Introduced at monomer coupling or ring-forming step, followed by purification for electronic-grade material processing

    Final product types

    • Precursor monomers for conductive films
    • Functionalized polymers for OLED displays
    • Organic thin-film transistors (OTFTs)

    5. Agrochemical Active Ingredient Synthesis

    This compound serves as a functionalized building block in certain pyrrole-derived agrochemical APIs, particularly in the synthesis of fungicide and insecticide molecules. The structure enables downstream cyclization or alkylation, yielding actives with selective soil mobility or bioactivity. Agrochemical manufacturers handle all synthesis steps within closed, validated environments to meet regulatory audit requirements.

    Industry compliance standards

    • FAO/WHO specifications for agricultural pesticides
    • US EPA 40 CFR Part 180 (tolerances for pesticide chemicals in food)
    • REACH registration where applicable
    • ISO 9001-based QMS for agrochemical production

    Typical usage ratio

    • 1.0–3.0 molar equivalents per API batch, optimized for target formulation and downstream stability

    Downstream process integration

    • Added during initial heterocyclic core assembly or late-stage functionalization in technical-grade synthesis

    Final product types

    • Pyrrole-based fungicide actives
    • Intermediate compounds for insecticidal formulations
    • Precursor for agrochemical analytical standards
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