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Ethyl 3-Amino-4-Pyrazolecarboxylate

    • Product Name Ethyl 3-Amino-4-Pyrazolecarboxylate
    • Alias Ethyl 3-amino-1H-pyrazole-4-carboxylate
    • Einecs 487-431-7
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry sales7@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    756935

    Product Name Ethyl 3-Amino-4-Pyrazolecarboxylate
    Cas Number 22483-09-6
    Molecular Formula C6H9N3O2
    Molecular Weight 155.16 g/mol
    Appearance White to off-white crystalline powder
    Melting Point 147-150°C
    Boiling Point No data available
    Solubility Slightly soluble in water, soluble in organic solvents
    Purity Typically ≥98%
    Storage Conditions Store in a cool, dry place, tightly closed
    Smiles CCOC(=O)C1=C(NN=C1)N
    Inchi InChI=1S/C6H9N3O2/c1-2-11-6(10)4-3-5(7)9-8-4/h3H,2,7H2,1H3,(H2,8,9)
    Synonyms Ethyl 3-amino-1H-pyrazole-4-carboxylate
    Refractive Index No data available
    Density No data available

    As an accredited Ethyl 3-Amino-4-Pyrazolecarboxylate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The packaging for Ethyl 3-Amino-4-Pyrazolecarboxylate (25g) is a sealed amber glass bottle with a printed chemical label.
    Shipping Ethyl 3-Amino-4-Pyrazolecarboxylate is shipped in sealed, chemical-resistant containers under ambient conditions. It is labeled according to regulatory standards, with safety documentation provided. The package is handled with care to prevent leaks or contamination. Transport complies with applicable chemical handling and shipping regulations to ensure safe delivery.
    Storage **Ethyl 3-Amino-4-Pyrazolecarboxylate** should be stored tightly sealed in a cool, dry, well-ventilated area away from heat, ignition sources, and incompatible substances such as strong oxidizers. Keep container tightly closed to prevent moisture absorption. Store at room temperature and protect from direct sunlight. Ensure proper labeling and segregation from food and drink. Follow all relevant chemical safety guidelines.
    Application of Ethyl 3-Amino-4-Pyrazolecarboxylate

    Applications of Ethyl 3-Amino-4-Pyrazolecarboxylate in Industrial Manufacturing

    Ethyl 3-Amino-4-Pyrazolecarboxylate serves as a key intermediate for several specialized industrial manufacturing processes, particularly in advanced chemical synthesis where its unique structure and reactivity enable access to high-value materials. As a dedicated manufacturer, we supply this compound to downstream producers who demand reliable quality and consistent performance to support specialized end-product categories. Below we detail the principal application areas, with specific focus on standardized practices, formulation roles, processing stages, and the resulting finished goods.

    1. Synthesis of Agrochemical Active Ingredients

    Producers of modern crop protection chemicals rely on this intermediate for constructing pyrazole-based herbicides and fungicides. Its unique aminopyrazole scaffold enables efficient introduction of functional groups needed for final actives, enhancing target specificity in high-performance formulations. Production lines integrate our material during early-stage functionalization, supporting batch-scale or continuous synthesis under GMP-aligned protocols to control impurities and isomeric purity for regulatory registration.

    Industry compliance standards

    • ISO 9001:2015 (Quality Management Systems in chemical manufacturing)
    • FAO/WHO specifications for pesticide ingredients and impurities
    • REACH Annex XVII and CLP (EU chemical safety)
    • EPA FIFRA guidelines for new active substances (USA)

    Typical usage ratio

    • 10–20% of total intermediate feed for target actives, fine-tuned according to the desired crop protection molecule and synthetic route.

    Downstream process integration

    • Direct incorporation during nucleophilic substitution or condensation to assemble the pyrazole core of specific herbicides or fungicides.

    Final product types

    • Selective herbicides for cereal and row crops
    • Systemic fungicides for fruit and vegetable protection
    • Molecular building blocks for further agrochemical derivatization

    2. Pharmaceutical Intermediates for Pyrazole-Based APIs

    Active pharmaceutical ingredient (API) manufacturers select this compound for synthesis routes involving substituted pyrazoles, a motif recurrent in anti-inflammatory and antipyretic drugs. High purity and traceability are imperative due to downstream regulatory audits; the compound enters API pipelines at the pyrazole ring-building phase, often under ICH Q7-compliant documentation and validated production controls.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice Guide for Active Pharmaceutical Ingredients
    • USP/NF and Ph. Eur monographs for pyrazole derivatives (where applicable)
    • EMA and FDA DMF submission requirements
    • ISO 13485 for supporting medical drug-device combination products

    Typical usage ratio

    • 15–30% of pyrazole ring-forming step mass balance; adjusted per API synthetic route and impurity control protocols.

    Downstream process integration

    • Fed into multi-step synthesis following organometallic catalysis or amidation to yield target pharmaceutical intermediates or final APIs.

    Final product types

    • Anti-inflammatory and analgesic APIs based on pyrazole pharmacophores
    • Intermediate compounds for custom-tuned therapeutic agents
    • Precursor materials for combinatorial drug discovery pipelines

    3. Building Block for Dye and Pigment Synthesis

    Manufacturers of specialty dyes and technical pigments utilize this material to introduce the pyrazole motif, valued for enhancing chromophore stability and color specificity in textile, printing, and plastic coloring applications. The intermediate is integrated into synthesis operations that require precise ring-forming reactions; its structure enables fine control of electronic effects, supporting the design of high-intensity and lightfast pigment molecules.

    Industry compliance standards

    • OEKO-TEX Standard 100 (textile dye safety)
    • EN 71-3 (Safety of toy pigments)
    • ISO 9001:2015 for pigment manufacturing consistency
    • REACH regulations for azo derivatives

    Typical usage ratio

    • 5–12% per chromophore intermediate batch; adjusted to achieve targeted hue intensity and chemical stability.

    Downstream process integration

    • Introduced during aromatic ring-condensation or heterocycle formation to access specialty pyrazole dyes or pigment precursors.

    Final product types

    • Disperse dyes for synthetic fiber textiles
    • Organic pigments for plastic coloration
    • Printing inks with high weather resistance

    4. Fine Chemical Synthesis for Specialty Materials

    Producers of specialty fine chemicals employ this compound as a foundation for creating advanced molecules used in research, photoinitiators, and electronics additives. Its highly reactive sites enable rapid incorporation into synthetic platforms that require custom modification of pyrazole groups, facilitating product innovation for emerging material science requirements.

    Industry compliance standards

    • ISO 14001:2015 (Environmental Management in specialty manufacturing)
    • Chemical safety data reporting under national and local regulations
    • RoHS (Restriction of Hazardous Substances, applicable to electronics additives)
    • Customer-specific purity and trace metal thresholds

    Typical usage ratio

    • 8–18% depending on the desired fine chemical product and target substitution pattern; composition validated by NMR and GC-MS analyses.

    Downstream process integration

    • Added at initial substrate formation or at late-stage derivatization to introduce customized pyrazole groups into specialty molecules.

    Final product types

    • Photoinitiators for UV-curable coatings
    • Electronic circuit additives and dopants
    • Structure-directing agents in advanced material synthesis
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