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Ethyl (ethoxymethylene)cyanoacetate

    • Product Name Ethyl (ethoxymethylene)cyanoacetate
    • Alias EEMCA
    • Einecs 245-007-1
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry sales6@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
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    Specifications

    HS Code

    633554

    Chemical Name Ethyl (ethoxymethylene)cyanoacetate
    Cas Number 94-05-3
    Molecular Formula C8H11NO3
    Molecular Weight 169.18 g/mol
    Appearance Yellow to orange liquid
    Boiling Point 163-164°C (at 13 mmHg)
    Melting Point -8°C
    Density 1.111 g/cm³ at 25°C
    Solubility Soluble in organic solvents such as ethanol and acetone
    Refractive Index 1.466-1.470
    Flash Point 129°C
    Synonyms Ethoxymethylenecyanoacetic acid ethyl ester
    Storage Conditions Store in a cool, dry, well-ventilated area

    As an accredited Ethyl (ethoxymethylene)cyanoacetate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 250g of Ethyl (ethoxymethylene)cyanoacetate is supplied in a tightly sealed amber glass bottle with hazard labeling and safety data.
    Shipping Ethyl (ethoxymethylene)cyanoacetate should be shipped in tightly sealed containers, protected from moisture and light. It must comply with chemical handling regulations—label as a hazardous material if required. Use appropriate secondary containment and padding, and include all relevant safety documents. Store and ship at ambient temperature, away from incompatible substances.
    Storage Ethyl (ethoxymethylene)cyanoacetate should be stored in a tightly sealed container in a cool, dry, and well-ventilated area away from heat, sparks, and direct sunlight. Keep it away from incompatible substances such as strong oxidizing agents and acids. Store under inert gas if possible to prevent moisture absorption and hydrolysis. Always follow standard chemical storage safety protocols and local regulations.
    Application of Ethyl (ethoxymethylene)cyanoacetate

    Applications of Ethyl (ethoxymethylene)cyanoacetate in Industrial Manufacturing

    Ethyl (ethoxymethylene)cyanoacetate acts as a specialty chemical intermediate essential in pharmaceutical synthesis, agrochemical active ingredient preparation, pigment and dye manufacturing, specialty coating additives, and other downstream production processes. As a direct manufacturer, we supply large-volume and consistent-grade material tailored to support controlled-scale industrial operations requiring advanced chemical intermediates.

    1. Pharmaceutical Intermediate for Active Ingredient Synthesis

    Major pharmaceutical manufacturers use this compound as a key building block in the synthesis of several heterocyclic pharmaceutical actives, notably in barbiturate and pyrimidine derivative synthesis. The material participates in Knoevenagel or Michael addition reactions during early-stage API manufacturing. Its reactivity and selective functionalization allow formulators to control the final API’s purity and yield, where end-use targets include anti-epileptic and sedative agents. Downstream partners integrate this intermediate at multi-hundred-kilogram scale to meet the controlled conditions required by global medicinal synthesis.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • EU EudraLex Volume 4 GMP, Part II
    • 21 CFR Part 210/211 US FDA Drug GMP
    • Pharmacopoeial monographs where applicable (USP/Ph. Eur. for downstream APIs)

    Typical usage ratio

    • Used at 0.8–1.05 molar equivalents relative to core amines or urea components; adjustment based on the desired substitution and API process yield requirements.

    Downstream process integration

    • Introduced at the condensation/formation step for heterocycle synthesis, following raw material verification and inline quality screening, ensuring trace reagent profiles match specification before combining with amine or carbonyl reagents.

    Final product types

    • Pharmaceutical active ingredients (e.g., phenobarbital, primidone)
    • Registered pharmaceutical intermediates
    • Contract-manufactured bulk APIs

    2. Agrochemical Intermediate for Pyrimidine and Triazine Herbicides

    Global agrochemical producers rely on this intermediate for the custom synthesis of pyrimidine and triazine ring systems, serving as a precursor in selective herbicide and plant growth regulator production lines. The substrate’s high chemical purity and reactivity simplify downstream cyclization and chlorination stages, enabling precise control of target activity and environmental compatibility. Formulators benefit from lot-to-lot reproducibility and validated impurity profiles that contribute to regulatory approval success.

    Industry compliance standards

    • FAO/WHO Specifications for plant protection products
    • OECD Guidelines for the Testing of Chemicals (for impurity and residue analysis)
    • ISO 9001:2015 Quality Management System (for batch release documentation)
    • REACH Regulation (EC) No 1907/2006 (for EU registration dossiers)

    Typical usage ratio

    • Typically dosed at 1.05–1.2 equivalents to diketone or amidine reactants; the ratio varies depending on ring fusion steps and desired crop safety margins documented in formulation records.

    Downstream process integration

    • Fed directly into the coupling reaction vessels, after substrate pre-charge and residual solvent checks; QA oversight includes HPLC confirmation of loading accuracy and interim conversion checks for consistent product attributes.

    Final product types

    • Pyrimidine-based herbicide actives (e.g., pyrithiobac-sodium)
    • Triazine herbicides
    • Pre-mix technical concentrates for post-synthesis formulation

    3. Specialty Dye and Pigment Intermediate

    Producers of high-performance organic dyes and specialty pigments utilize ethyl (ethoxymethylene)cyanoacetate in the stepwise synthesis of azo, anthraquinone, and phthalocyanine-based colorants. The intermediate's electron-withdrawing cyano group aids in achieving higher chroma, shade consistency, and stability for application in plastics and printing inks requiring strict shade repeatability. Its controlled addition during mono- and di-substitution reactions allows precise tuning of final pigment performance attributes and dispersibility.

    Industry compliance standards

    • ISO 9001:2015 Quality Management System (for colorant consistency)
    • EN 71-3 Safety of Toys – Migration of certain elements (for pigment use in toys)
    • OEKO-TEX® Standard 100 (for textile end-uses, pigment certification)
    • Environmental Protection Law GB 8978–1996 (for effluent control in China)

    Typical usage ratio

    • Applied within 2–15% by mole fraction in the targeted coupling/complexation stage, based on color intensity required and side-chain substitution constraints observed during pre-shipment sample approval.

    Downstream process integration

    • Precision-dosed into the primary aromatic coupling or ring-closure process, usually after pre-drying and sieve validation; downstream pigment development frequently monitors unconverted intermediate residues via UV/Vis or GC analytics.

    Final product types

    • High-stability industrial pigments
    • Specialty dyes for plastics processing
    • Organic colorants for high-speed inkjets

    4. Intermediate for UV-Curable and Specialty Polymer Additives

    Leading formulation chemists in UV-cured coating and advanced polymer composites industries apply this intermediate in the design of specialty monomers and oligomers. It introduces both electron-deficient and solubilizing groups essential for photoreactivity and crosslink density control. As an additive in pre-polymer production, the material guarantees a defined functional density, impacting end-use properties such as cure rate, environmental resistance, and mechanical performance—particularly for electronics encapsulation and automotive applications.

    Industry compliance standards

    • ISO 14001:2015 (for environmental impact of coatings formulation and effluent treatment)
    • RoHS Directive (2011/65/EU) for electronics compatibility
    • REACH Registration (substance and downstream user notification)
    • ASTM D7767 (Standard test method for polymer UV curing properties)

    Typical usage ratio

    • Used at 0.5–2.0% by total solid weight in oligomer synthesis or downstream as 1–5% reactive diluent; dosage adjusted by reactivity profiles established during pilot-scale compounding.

    Downstream process integration

    • Added during the prepolymerization step, following solvent stripping and baseline reactivity calibration using test-batch initiators; integration documented per lot for traceability and QC records.

    Final product types

    • UV-cured coatings for electronics
    • Specialty photoresist materials
    • Crosslinked polymer encapsulants and adhesives

    5. Intermediate for Fine Chemical and Custom Synthesis Services

    Chemical contract manufacturers and research-driven production sites use this intermediate as a versatile precursor in small molecule, ligand, and specialty fine chemical synthesis. Its controlled reactivity profile allows process chemists to customize downstream products in accordance with customer specifications and project milestones. Batch-based synthesis benefits from real-time monitoring of conversion efficiency, ensuring that substructure transformation aligns with the precise parameters set out in toll manufacturing or custom synthesis agreements.

    Industry compliance standards

    • ISO 9001:2015 Quality Management System (documented process controls)
    • cGMP Guidelines as specified by end-user (when used as secondary intermediates)
    • REACH and country-specific chemical control lists for specialty chemical handling
    • Confidentiality and data integrity protocols for CDMO projects

    Typical usage ratio

    • Usage determined by project scope; often 1.0–1.2 molar equivalents in defined condensation or functionalization steps per route design, agreed within the scope of the project’s synthetic pathway.

    Downstream process integration

    • Received and stored per project-specific batch tracking; introduced following analytical verification in multi-step synthesis or used in one-pot routes where reaction sequence stability is controlled and documented for each unique project.

    Final product types

    • Custom fine chemicals
    • Specialized ligand-building blocks
    • High-value research and development intermediates
    Free Quote

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    Tel: +8618018036652

    Email: sales6@sinochem-nanjing.com

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