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Ethyl 3-Aminocrotonate

    • Product Name Ethyl 3-Aminocrotonate
    • Alias Ethyl 3-aminobut-2-enoate
    • Einecs 209-781-3
    • 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

    707332

    Chemical Name Ethyl 3-Aminocrotonate
    Cas Number 16532-79-9
    Molecular Formula C6H11NO2
    Molecular Weight 129.16 g/mol
    Appearance Colorless to yellow liquid
    Boiling Point 207-208 °C
    Density 1.037 g/mL at 25 °C
    Melting Point -13 °C
    Solubility Soluble in organic solvents such as ethanol, ether
    Purity Typically ≥98%
    Refractive Index n20/D 1.446
    Flash Point 90 °C (closed cup)
    Synonyms Ethyl 3-aminobut-2-enoate
    Smiles CCOC(=O)C=C(N)C
    Storage Conditions Store at 2-8 °C, tightly closed

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

    Packing & Storage
    Packing Ethyl 3-Aminocrotonate, 100g, packaged in a sealed amber glass bottle with tamper-evident cap, labeled with hazard and safety information.
    Shipping Ethyl 3-Aminocrotonate should be shipped in tightly sealed containers to avoid moisture and contamination, typically under ambient temperatures. It must comply with applicable chemical transport regulations and be clearly labeled. Transport in accordance with safety guidelines, ensuring protection from physical damage, and keeping away from incompatible substances or extreme temperature variations.
    Storage **Ethyl 3-aminocrotonate** should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area. Keep it away from heat sources, direct sunlight, and incompatible materials such as strong oxidizing agents. Store at room temperature, ideally below 25°C. Properly label the container and avoid moisture exposure to maintain chemical integrity and ensure safe handling.
    Application of Ethyl 3-Aminocrotonate

    Applications of Ethyl 3-Aminocrotonate in Industrial Manufacturing

    Ethyl 3-Aminocrotonate serves as a crucial intermediate in multiple high-value chemical production chains, supporting specialized downstream industries that demand precise input specifications, regulatory conformity, and reliable scalability. As a direct manufacturer, we ensure controlled purity and consistent supply to enable integration into advanced synthesis workflows.

    1. Pharmaceutical Intermediate for Pyrimidine Synthesis

    In pharmaceutical manufacturing, this intermediate plays an irreplaceable role in the preparation of pyrimidine derivatives, particularly active pharmaceutical ingredients (APIs) for antiviral and anticancer therapies. Responding to diverse molecule designs, formulators fine-tune input ratios based on targeted reaction yields in their synthetic routes, reserving tight control over all incoming batch attributes. Downstream production integrates our material during the first step of multi-stage condensation reactions, where aminocrotonate acts as the core building block under monitored pH and solvent conditions, ensuring reproducible heterocycle formation. Final product portfolios primarily include cytidine analogues, nucleotide-based compounds, and intermediates for high-potency small-molecule APIs supplied to global generic and branded drug markets.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP–NF and European Pharmacopoeia monographs (where applicable to synthesized APIs)
    • EU Registration, Evaluation, Authorisation and Restriction of Chemicals (REACH)
    • US FDA 21 CFR Part 211 (Current Good Manufacturing Practice for Finished Pharmaceuticals)

    Typical usage ratio

    • 10–35 mol% relative to other core reactants, optimized per molecular pathway; adjusted by reaction yield and process scale

    Downstream process integration

    • Charged at initial condensation or nucleophilic addition steps within multi-stage synthesis of pyrimidine scaffolds; handled under inert conditions to preserve purity prior to cyclization

    Final product types

    • Pharmaceutical pyrimidine derivatives (e.g., APIs for antivirals and cancer treatments)
    • Intermediates for contract synthesis
    • Finished cytidine analogues

    2. Agrochemical Intermediate for Fungicide and Herbicide Synthesis

    Downstream agrochemical producers incorporate this specialty raw material as a precursor for synthesizing selective fungicides and herbicides, where efficient nitrogen incorporation and stable ester functionality are essential for targeted biological activity. The material enters formulation trains at the controlled amidation or cyclization stage, where its conversion efficiency directly determines the yield and purity of final actives. Formulators typically align the inclusion ratio according to desired batch output and the stoichiometry of complementary substrates. These processes lead to formulation of high-performance agrochemicals distributed for row crop protection and specialty applications.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • ISO 9001:2015 Quality Management System
    • EU REACH and CropLife International guidelines for safe chemical handling
    • OECD Principles of Good Laboratory Practice (GLP) for agrochemical R&D

    Typical usage ratio

    • 15–25 weight% relative to main synthesis batch, adjusted based on specific fungicide or herbicide being synthesized

    Downstream process integration

    • Dosed into continuous or batch reactors during initial condensation and ring-forming steps; further processed through purification, crystallization, and formulation

    Final product types

    • Triazole-based fungicides
    • Pyrimidinyl herbicides
    • Intermediate concentrate for granulated or liquid crop protection formulations

    3. Intermediate in Dye and Pigment Synthesis

    Dye manufacturers rely on the unique conjugated structure of this intermediate for building complex heterocyclic dye molecules that must exhibit specific chromatic properties and lightfastness in textile and ink applications. The compound integrates in diazotization or condensation reactions at an early stage, where its amino crotonate moiety drives selective coupling with aromatic partners. Technicians adjust the input proportion to regulate hue intensity and pigment concentration in end-use dispersions. Downstream facilities deploy in-line analytical checks to ensure that color consistency and fastness parameters meet customer requirements for pigment pastes, concentrates, and finished textile dyes supplied to high-specification markets.

    Industry compliance standards

    • Oeko-Tex Standard 100 for textile safety
    • REACH Regulation (EC 1907/2006) registration for industrial use in Europe
    • ISO 9001 and ISO 14001 for process and environmental management
    • GOTS for organic textile dye components (when used in certified processes)

    Typical usage ratio

    • 8–20 mol% relative to aromatic or diazo partners within the target dye molecule; ratio tuned to achieve precise color shade and depth

    Downstream process integration

    • Introduced during core dye synthesis (e.g., for coupling and cyclization), followed by isolation, purification and standard pigment dispersion

    Final product types

    • Monoazo and heterocyclic textile dyes
    • High-performance printing inks
    • Dispersed pigment concentrates for fiber and plastic coloration

    4. Building Block for Fine Chemical Synthesis (Flavor & Fragrance Ingredients)

    In fine chemical production, particularly for aroma and flavor intermediates, this compound is valued for its amino ester backbone, enabling efficient chiral and structural elaboration. Specialty ingredient manufacturers charge it during the controlled condensation and cyclization stages, using precise input ratios that vary according to the stereochemistry and length of synthetic sequences. Its role directly influences the olfactory and gustatory attributes of natural-identical aroma chemicals and flavor enhancers. Downstream process engineers monitor purity specifications tightly, since low-level impurities can alter scent and taste perception profiles in sensory-critical products that must pass both regulatory review and customer panel testing.

    Industry compliance standards

    • FEMA (Flavor and Extract Manufacturers Association) GRAS substances compendium
    • IFRA Standards for fragrance material safety
    • EU Foods Regulation (EC) No 1334/2008 for flavorings
    • ISO 22000 Food Safety Management System (for food-contact grades)

    Typical usage ratio

    • 5–18 mol% depending on end molecule complexity; optimization based on batch-to-batch reactivity and desired throughput

    Downstream process integration

    • Added at early ring closure or amidation steps, followed by selective elaboration toward target aromatic or flavor compounds, with subsequent distillation and purification

    Final product types

    • Flavor enhancers for beverages and confections
    • Specialty fragrance ingredients for personal care and home care
    • Natural-identical aroma compounds for fine fragrances and air fresheners
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