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Diethyl Acetylmalonate

    • Product Name Diethyl Acetylmalonate
    • Alias Diethyl 3-acetyl-2-oxobutanedioate
    • Einecs 204-542-0
    • 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

    849335

    Chemical Name Diethyl Acetylmalonate
    Cas Number 609-09-6
    Molecular Formula C9H14O5
    Molecular Weight 202.20
    Appearance Colorless to pale yellow liquid
    Boiling Point 125-127 °C (15 mmHg)
    Density 1.13 g/cm3 at 20 °C
    Refractive Index 1.435-1.437
    Melting Point -7 °C
    Solubility Soluble in organic solvents, slightly soluble in water
    Synonyms Acetylmalonic acid diethyl ester
    Flash Point 117 °C
    Smiles CCOC(=O)CC(C(=O)OCC)C=O

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

    Packing & Storage
    Packing A 250 mL amber glass bottle securely sealed, labeled “Diethyl Acetylmalonate,” with hazard symbols and detailed handling/storage instructions.
    Shipping Diethyl Acetylmalonate is shipped in tightly sealed containers, typically glass or plastic, to prevent moisture and air exposure. It is transported as a chemical under standard regulations, with labeling for flammability and health hazards. Store and ship in a cool, dry place, away from incompatible substances and ignition sources.
    Storage Diethyl acetylmalonate should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from direct sunlight and incompatible materials such as strong oxidizers. It should be kept away from heat sources and ignition points. The storage area should be clearly labeled and equipped with spill containment measures to prevent environmental contamination. Store at room temperature.
    Application of Diethyl Acetylmalonate

    Applications of Diethyl Acetylmalonate in Industrial Manufacturing

    Diethyl Acetylmalonate serves as a crucial fine chemical intermediate in a range of industrial sectors. As the direct manufacturer, we ensure material consistency for complex syntheses in pharmaceutical, agrochemical, dye, and specialty chemical production lines. Below, we detail real downstream use cases, compliance aspects, formulation guidelines, and integration in proven manufacturing environments.

    1. Pharmaceutical API Intermediate for Barbiturates

    API producers leverage this raw material during barbiturate and related pyrimidine synthesis due to its enolizable active methylene group and acetyl functionality. Facilities typically convert it via alkylation and cyclization steps, forming core scaffolds such as phenobarbital, secobarbital, or metharbital. Strict process segregation, complete lot traceability, and impurity profiling anchor its use in regulated pharmaceutical supply chains.

    Industry compliance standards

    • EU GMP Part II (ICH Q7: Good Manufacturing Practice for Active Pharmaceutical Ingredients)
    • United States Pharmacopeia (USP) Reference Standards
    • EDQM CEP for intermediates in EU submissions
    • FDA 21 CFR Part 211 (for intermediates used on-site in drug substance production)

    Typical usage ratio

    • 0.85–1.10 molar equivalents, tailored by specific downstream API synthesis; adjustment based on desired product purity and process yield.

    Downstream process integration

    • Direct input for enolate alkylation during barbiturate scaffold assembly
    • Integrated into continuous stirred-tank reactors, in presence of sodium alkoxide base
    • Subject to in-process HPLC and GC monitoring for acetyl group integrity

    Final product types

    • Barbiturate sedative-hypnotic Active Pharmaceutical Ingredients (APIs)
    • Pyrimidine-based diagnostic compounds
    • Pharmaceutical grade reference standards

    2. Agrochemical Synthesis – Herbicide and Fungicide Intermediates

    Crop protection manufacturers employ this compound for constructing substituted pyrimidones and triketone intermediates, used in selective herbicides and fungicides. Formulators benefit from high chemical yield and ease of acyl group transfer for targeted derivatization in seed treatment and foliar protection actives. Strict environmental and worker safety controls govern all production activities.

    Industry compliance standards

    • OECD Guidelines for the Testing of Chemicals
    • REACH Registration (EC 1907/2006) for use as a substance in plant protection active synthesis within the EU
    • FAO/WHO Good Laboratory Practice (GLP) for technical active ingredient manufacturing
    • China’s GB 2763—National Food Safety Standard for Maximum Residue Limits for Pesticides

    Typical usage ratio

    • 10–25% w/w of total starting material, depending on alkylation and acylation requirements per end molecule; operators adjust charge based on targeted downstream conversion and isolate yield.

    Downstream process integration

    • Feedstock for stepwise alkylation/acylation with amines and aromatic substrates
    • Combined with metal catalysts in batch reactors at elevated temperature (100–150°C)
    • Monitored for residual diethyl ester content before further derivatization

    Final product types

    • Isoxazolyl herbicides
    • Triketone agricultural fungicides
    • Pyrimidinone-based cereal protectants
    • Technical concentrates for agrochemical formulation plants

    3. Dye and Pigment Manufacturing – Heterocycle Intermediate

    Industrial colorant producers use diethyl acetylmalonate for synthesizing fluorophore and chromophore cores. Its high selectivity for aminomethylation and condensation gives access to complex heterocycles such as pyrazolo[1,5-a]pyrimidines and benzofurans, which serve as lightfast dyes for plastics, textiles, and inkjet printing. Manufacturers enforce color index registration and standardized batch approval testing.

    Industry compliance standards

    • ETAD (Ecological and Toxicological Association of Dyes and Organic Pigments Manufacturers) Risk Assessment Protocols
    • Oeko-Tex Standard 100 (for dyes on textiles)
    • ISO 9001 certified process control
    • REACH Annex XVII restrictions on dye use in plastics and consumer articles

    Typical usage ratio

    • 5–18% by mass in pigment precursor blends, based on chromophore complexity and solubilizer loading per downstream processing batch.

    Downstream process integration

    • Input into multistep condensation with aromatic diamines under acid catalysis
    • Thermal coupling in controlled pH to yield pigment intermediate
    • Purification via recrystallization or continuous solvent extraction

    Final product types

    • Inkjet printing dyes
    • Textile-reactive pigments
    • High-stability plastics colorants
    • Automotive coating pigment dispersions

    4. Specialty Chemicals – Perfume and Flavor Intermediate

    Aromatic compound manufacturers introduce diethyl acetylmalonate to synthesize functionalized cyclopentenolone derivatives, serving as key intermediates for musk and sweet, caramelized flavoring agents. The malonate structure facilitates controlled cyclization and selective functionalization steps, allowing flavor houses and perfumers to achieve reproducible aroma profiles in accordance with international food and cosmetic safety standards.

    Industry compliance standards

    • IFRA Code of Practice for fragrance ingredient use
    • US FDA 21 CFR §172.515 (Flavoring Substances and Adjuvants permitted for direct addition to food)
    • FAO JECFA (Joint FAO/WHO Expert Committee on Food Additives) flavor additive safety evaluation
    • ISO 22000:2018 Food Safety Management in chemical flavor production

    Typical usage ratio

    • 0.5–3.2% relative to total formulation input, optimized for desired fragrance intensity and volatility profile per end product requirement.

    Downstream process integration

    • Cyclization under mild acid catalysis in glass-lined kettles
    • Functionalization with alkyl or aryl halides prior to incorporation into aroma concentrate
    • Final material screened for purity via GC-MS and organoleptic evaluation

    Final product types

    • Cosmetic perfumery bases (musk, floral, caramel)
    • Natural and nature-identical flavoring agents for confectionery
    • Beverage flavor concentrates
    • Encapsulated fragrance microcapsules for detergents
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