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Diethyl 2-(2-Cyanoethyl)Malonate

    • Product Name Diethyl 2-(2-Cyanoethyl)Malonate
    • Alias DEM
    • Einecs EINECS 237-247-9
    • 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
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    Specifications

    HS Code

    814491

    Chemicalname Diethyl 2-(2-Cyanoethyl)Malonate
    Molecularformula C10H15NO4
    Molecularweight 213.23 g/mol
    Casnumber 20320-59-6
    Appearance Colorless to pale yellow liquid
    Boilingpoint 180-182°C at 6 mmHg
    Density 1.112 g/mL at 25°C
    Refractiveindex 1.433-1.435
    Solubility Slightly soluble in water; soluble in organic solvents
    Purity Typically ≥98%
    Smiles CCOC(=O)C(CNCCC#N)C(=O)OCC
    Meltingpoint -6°C
    Storagetemperature 2-8°C

    As an accredited Diethyl 2-(2-Cyanoethyl)Malonate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 500g of Diethyl 2-(2-Cyanoethyl)Malonate is supplied in a tightly sealed amber glass bottle with a tamper-evident cap.
    Shipping **Shipping Description:** Diethyl 2-(2-Cyanoethyl)Malonate is shipped in tightly sealed containers, stored in a cool, dry, and well-ventilated area. Packaging complies with chemical safety regulations to prevent leaks or exposure. Proper labeling, including hazard and handling instructions, ensures safe transportation according to international and local shipping guidelines.
    Storage Diethyl 2-(2-Cyanoethyl)malonate should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from sources of ignition and incompatible substances such as strong oxidizers. Protect from moisture and direct sunlight. Store at room temperature, and ensure proper labeling. Handle in accordance with good chemical hygiene and safety practices to prevent spills and contamination.
    Application of Diethyl 2-(2-Cyanoethyl)Malonate

    Applications of Diethyl 2-(2-Cyanoethyl)Malonate in Industrial Manufacturing

    As an established manufacturer, we supply Diethyl 2-(2-Cyanoethyl)Malonate (DECM) to key segments within the advanced fine chemicals industry. Our expertise and production data ensure precise, real-world application guidance for downstream partners focusing on high-value synthesis sectors. Below, we detail verified, sector-specific uses to support technical users in decision-making and process control.

    1. Pharmaceutical Intermediate for Barbiturate Derivatives

    Specialty pharmaceutical manufacturers utilize DECM as a key intermediate in the synthesis of barbiturate APIs, facilitating the construction of complex ring systems required for central nervous system active agents. Its electron-withdrawing cyanoethyl group supports tailored reactivity in condensation stages, critical for producing consistent API quality.

    Industry compliance standards

    • USP, EP, JP pharmacopeial monographs for active ingredients
    • ICH Q7 Good Manufacturing Practice Guide
    • FDA cGMP (21 CFR Part 210/211) for API production
    • EU GMP Annex 1 for sterile synthesis intermediates

    Typical usage ratio

    • 0.8–1.2 molar equivalents relative to target barbituric core; adjustments depend on target molecule substitution patterns and yield optimization in condensation step

    Downstream process integration

    • Charged as a main building block during the Knoevenagel condensation stage with urea derivatives; further processed via cyclization and purification to yield the API structure

    Final product types

    • Pharmaceutical barbiturate APIs (e.g., phenobarbital, thiopental sodium)
    • Related CNS depressant drugs produced under regulated batch controls

    2. Agrochemical Intermediate for Pyridine-Based Herbicides

    Leading agrochemical groups employ DECM during the multi-step synthesis of pyridine-derived herbicides, utilizing its dual functional groups to establish specific substitution patterns essential for biological activity and selectivity in crop protection formulations.

    Industry compliance standards

    • FAO/WHO specification for technical pesticides
    • ISO 1750 (pesticide common names and identity)
    • REACH (EC) No 1907/2006 for agricultural raw chemicals
    • GLP (Good Laboratory Practice) for process impurity studies

    Typical usage ratio

    • 0.6–1.0 mol per target pyridine nucleus, with concentration adjusted to control reaction selectivity and impurity profile during key condensation or alkylation reactions

    Downstream process integration

    • Introduced after initial halogenation of pyridine rings; participates in nucleophilic addition, then removed by subsequent hydrolysis or decarboxylation under basic conditions

    Final product types

    • Pyridine-based herbicide active ingredients for selective weed control
    • Premixed herbicide technical concentrations for further formulation

    3. Monomer Building Block in Specialty Polymeric Materials

    Producers of high-performance polymers integrate DECM into copolymerization processes aimed at engineering specialty plastics with enhanced solvent resistance and thermal stability. Its unique structure introduces functional points for post-polymer modification, important for automotive and electronics applications.

    Industry compliance standards

    • ISO 9001:2015 for industrial quality management
    • ISO 14001:2015 for environmental process controls
    • RoHS for electrical/electronic polymer applications within the EU
    • ASTM D256, ASTM D638 for polymer mechanical performance

    Typical usage ratio

    • 5–15% by weight of total monomer feed; actual level calibrated against desired copolymer molecular weight and resulting glass transition temperature

    Downstream process integration

    • Fed as a monomer co-reactant during solution or suspension polymerization; participates in controlled radical or anionic propagation with acrylates or styrenic units

    Final product types

    • Specialty resins for automotive coatings and molded engine parts
    • High-performance films for electronic packaging or display technology

    4. Electronic Chemicals—Precursor for Functionalized Acrylics

    Manufacturers in the electronics sector use DECM to introduce cyanoalkyl side chains into advanced acrylic and methacrylic resins, tailoring dielectric properties vital for printed circuit board (PCB) coatings and microelectronic encapsulants. Controlled reactivity ensures batch-to-batch consistency for sensitive electronic assembly.

    Industry compliance standards

    • IPC-4101 (laminate and prepreg material quality)
    • IEC 61249 for PCB base materials
    • JIS C 5018 for electronic resin applications in Japan
    • REACH safety handling and registration for electronic chemicals

    Typical usage ratio

    • 3–7% by weight of resin formulation; fine-tuned based on required dielectric constant and mechanical property targets

    Downstream process integration

    • Introduced during pre-polymer mixing; participates in chain extension reactions and is grafted onto resin backbones via solution or bulk polymerization

    Final product types

    • Photoimageable solder mask resins for advanced PCB fabrication
    • Dielectric coatings and encapsulant formulations for ICs and semiconductor substrates

    5. Fine Chemical Synthesis for Active Ingredient Intermediates

    In the fine chemical industry, DECM acts as a controlled reactant for custom syntheses where cyanoalkyl functionalization is required—enabling downstream construction of pharmaceutical, agrochemical, and specialty compound scaffolds where direct malonate alkylation can simplify multi-step routes.

    Industry compliance standards

    • ISO 9001:2015 for quality management systems in fine chemicals
    • Custom synthesis subject to client standard operating procedures and regulatory requirements for each target molecule
    • REACH and TSCA inventory status for exported intermediates
    • Environmental and safety compliance per GHS labeling and SDS documentation

    Typical usage ratio

    • 0.7–1.3 equivalents, determined by route-specific stoichiometry and stepwise yield improvement goals under client process development protocols

    Downstream process integration

    • Dosed directly into initial condensation or alkylation step; controlled addition may precede further reduction, hydrolysis, or ring closure as required by end-user’s molecule target

    Final product types

    • Multi-functional intermediates for confidential pharmaceutical or crop protection pipelines
    • Building blocks for custom catalog synthesis and contract fine chemical manufacturing
    Free Quote

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