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2-(2-Aminothiazole-4-Yl)-2-Hydroxyiminoacetic Acid

    • Product Name 2-(2-Aminothiazole-4-Yl)-2-Hydroxyiminoacetic Acid
    • Alias ATHA
    • Einecs EINECS 417-360-6
    • 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

    730947

    Cas Number 128938-60-1
    Molecular Formula C5H5N3O3S
    Molecular Weight 187.18
    Appearance Solid
    Purity Typically ≥98%
    Solubility Soluble in DMSO, slightly soluble in water
    Structure Thiazole ring with amino and hydroxyiminoacetic acid substituents
    Iupac Name 2-(2-amino-1,3-thiazol-4-yl)-2-hydroxyiminoacetic acid
    Storage Temperature 2-8°C (Refrigerated)
    Logp -0.99
    Pka 2.2 (carboxylic acid group, estimated)

    As an accredited 2-(2-Aminothiazole-4-Yl)-2-Hydroxyiminoacetic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The packaging is a 5g amber glass vial, sealed with a screw cap, featuring a printed chemical label and hazard warnings.
    Shipping The chemical 2-(2-Aminothiazole-4-yl)-2-hydroxyiminoacetic acid is shipped in tightly sealed containers, protected from light and moisture, and complies with relevant hazardous material regulations. Proper labeling and documentation ensure safe handling during transport. Temperature control and secondary containment may be used to prevent spills, contamination, or degradation during shipping.
    Storage Store **2-(2-Aminothiazole-4-yl)-2-hydroxyiminoacetic acid** in a tightly sealed container, protected from light and moisture. Keep at a cool temperature, ideally at 2-8°C (refrigerated), and away from incompatible substances such as strong oxidizing agents. Ensure the storage area is well-ventilated and clearly labeled. Follow institutional and safety guidelines for handling and disposal.
    Application of 2-(2-Aminothiazole-4-Yl)-2-Hydroxyiminoacetic Acid

    Applications of 2-(2-Aminothiazole-4-Yl)-2-Hydroxyiminoacetic Acid in Industrial Manufacturing

    Our facility manufactures 2-(2-Aminothiazole-4-Yl)-2-Hydroxyiminoacetic Acid for industrial customers who require a high-purity intermediate in precise, complex production environments. This compound serves in advanced chemical synthesis across distinct sectors, where specification compliance, process reliability, and downstream performance are tightly controlled. The following sections detail established, differentiated applications in today’s chemical and pharmaceutical industries.

    1. Active Pharmaceutical Ingredient (API) Intermediate for Cephalosporin Antibiotic Synthesis

    This compound is widely implemented as a key intermediate in the multi-step synthesis of certain third-generation cephalosporin antibiotics. Its precise incorporation supports nucleophilic coupling reactions and ensures the required thiazole moiety is introduced with strict stereo-chemical control. Pharmaceutical manufacturers rely on defined specifications and validated process steps to meet international drug quality and safety requirements.

    Industry compliance standards

    • ICH Q7 – Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP (United States Pharmacopeia) Quality Standards
    • European Pharmacopoeia (Ph. Eur.) Monographs
    • US FDA GMP Regulations (21 CFR Parts 210, 211)

    Typical usage ratio

    • Integrated at 0.8–1.2 molar equivalents, adjusted based on desired yield and impurity profile management in the antibiotic core assembly process.

    Downstream process integration

    • Charged after initial β-lactam ring construction, before thiazole ring condensation.
    • Dissolved in deionized solvent under nitrogen with temperature and pH control, enabling real-time monitoring of conversion and byproduct suppression.
    • Purification via preparative crystallization or column chromatography prior to API amide coupling.

    Final product types

    • Oral and injectable third-generation cephalosporin formulations (e.g., cefotaxime, ceftriaxone)
    • Lyophilized antibiotic powders for reconstitution
    • Bulk sterile intermediates for onward pharmaceutical formulation

    2. Intermediate for Advanced Agrochemical Synthesis

    Chemical producers utilize this material in the stepwise formation of thiazole-containing herbicide and fungicide actives. Its reactivity profile enables selective oxime and amination reactions, supporting the tailored construction of active moieties that comply with crop protection legislation in major agricultural markets.

    Industry compliance standards

    • FAO/WHO Specifications (JMPS guidelines)
    • ISO 9001:2015 Quality Management
    • EPA Pesticide Registration Requirements (40 CFR 152–180)

    Typical usage ratio

    • Used at 3–7% w/w relative to total batch mass for target triazole- or thiazole-skeleton synthesis, with ratios refined for each crop application and regulatory residue constraints.

    Downstream process integration

    • Added during the nucleophilic substitution or cyclization phase after diketone pre-assembly, supporting precise heterocycle formation and side chain attachment.
    • Batch parameters adjusted for solvent compatibility and hydrolysis prevention.
    • Post-synthesis purification by recrystallization before formulation into commercial concentrates.

    Final product types

    • Broad-spectrum fungicidal actives (thiazole derivatives)
    • Systemic herbicide active ingredients
    • Technical-grade agrochemical intermediates for downstream formulators

    3. Chemical Building Block for Specialty Dye Stuffs Manufacturing

    In the colorants industry, manufacturers incorporate this thiazole-based compound for its reliable electron-donating and chelating functionality, which imparts unique properties to high-performance azo and oxime dyes. Its application focuses on dye molecules engineered for resistance, solubility, and chromatic stability demanded by automotive, textile, and electronic substrate producers.

    Industry compliance standards

    • OEKO-TEX® Standard 100 (Textile chemical requirements)
    • REACH Registration and Safety Documentation
    • DIN EN ISO 105-E04 (Textile Color Fastness Tests)

    Typical usage ratio

    • 1.0–2.5 mol% as an interactive synthesis reagent relative to core chromogenic precursor; adjusted for targeted shade intensity and fastness properties.

    Downstream process integration

    • Dosed at the coupling or ligation reaction stage during dye backbone synthesis following diazotization.
    • Incorporation controlled to modulate bath pH and oxidative stability, with online HPLC tracking at the solid-liquid separation phase.

    Final product types

    • Reactive and acid dye powder blends for textile dye houses
    • Oxime-modified pigment dispersions for automotive coatings
    • Functionalized dye intermediates for electronic ink applications

    4. Research Intermediate in Fine Chemical and Material Science Laboratories

    Leading R&D laboratories and fine chemicals producers employ this molecule in the structure-directed synthesis and validation of customized thiazole and oxime scaffolds for discovery projects. Its consistent quality and precise functional groups allow repeatable experimental outcomes in pilot-scale runs relevant to pharmaceutical research and functional material development.

    Industry compliance standards

    • ISO/IEC 17025 (Testing and Calibration Laboratories)
    • GLP (Good Laboratory Practice) Principles
    • Internal quality specifications documented in project dossiers

    Typical usage ratio

    • Varies by synthetic route, typically 0.5–2 equivalents according to protocol design; adjusted to manage exploratory reaction yields and product identity targets.

    Downstream process integration

    • Weighing and addition at core condensation or oxime formation step in bench or kilo-lab scale projects.
    • Used under inert atmosphere or sealed glass equipment to minimize decomposition or side reaction pathways.
    • Process monitored with spectroscopic and chromatographic techniques to validate structure and scale-up feasibility.

    Final product types

    • Thiazole- and oxime-derived chemical scaffolds for lead compound screening
    • Reference standards for analytical method development
    • Pilot-batch specialty intermediates for integration in advanced material formulations
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