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Thiophene-3-Acetic Acid Hydrazide

    • Product Name Thiophene-3-Acetic Acid Hydrazide
    • Alias 3-Thiophenacetic acid hydrazide
    • Einecs 651-206-2
    • 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

    544866

    Product Name Thiophene-3-Acetic Acid Hydrazide
    Cas Number 26218-77-7
    Molecular Formula C6H8N2OS
    Molecular Weight 156.20
    Appearance White to off-white solid
    Melting Point 163-167°C
    Purity Typically ≥98%
    Solubility Soluble in DMSO, methanol
    Chemical Classification Heterocyclic compound; Hydrazide
    Synonyms 3-Thiopheneacetic acid hydrazide
    Storage Temperature 2-8°C
    Smiles C1=CSC=C1CC(=O)NN
    Inchikey CKTPWBJGGZVODB-UHFFFAOYSA-N

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

    Packing & Storage
    Packing Thiophene-3-Acetic Acid Hydrazide is supplied in a sealed amber glass bottle, 5 grams, with tamper-evident cap and safety labeling.
    Shipping Thiophene-3-Acetic Acid Hydrazide is typically shipped in tightly sealed, chemical-resistant containers to prevent moisture and contamination. It is dispatched under ambient conditions unless otherwise specified, with relevant safety documentation included. Handle with appropriate personal protective equipment and store away from strong oxidizers. Complies with applicable transport regulations for laboratory chemicals.
    Storage Thiophene-3-Acetic Acid Hydrazide should be stored in a tightly sealed container, kept in a cool, dry, and well-ventilated area away from sources of heat, ignition, and direct sunlight. Protect it from moisture and incompatible materials such as strong oxidizing agents. For optimal stability, store at 2-8°C (refrigerated) and ensure the container is clearly labeled.
    Application of Thiophene-3-Acetic Acid Hydrazide

    Applications of Thiophene-3-Acetic Acid Hydrazide in Industrial Manufacturing

    Thiophene-3-Acetic Acid Hydrazide serves as a specialized intermediate in several precision-driven industrial manufacturing fields. Our vertically integrated production approach ensures strict quality control matching the diverse regulatory environments and formulation practices of advanced downstream applications. Explore how this compound fits within high-value real-world manufacturing segments.

    1. Pharmaceutical Intermediate for Thiazole Synthesis

    This compound plays a crucial role in the synthesis of thiazole-derived APIs, especially in anti-infective and CNS-active pharmaceutical classes. Manufacturers rely on it for its reactivity in condensation and cyclization stages essential for building core pharmacophores. Strict adherence to international pharmacopoeial and GMP guidelines governs its use, with QC measures designed to mitigate process impurities at each batch stage. Finished APIs derived from these processes supply regulated markets in both solid and injectable formats.

    Industry compliance standards

    • ICH Q7A Good Manufacturing Practice Guidance
    • EU GMP (EudraLex Volume 4)
    • USP General Chapter <458> for chemical intermediates
    • WHO TRS 986 Annex 2 for APIs

    Typical usage ratio

    • 0.08–0.18 molar equivalents relative to key aldehydes or ketones, adjusted per synthesis route and target API yield recovery

    Downstream process integration

    • Introduced during the substrate activation or early condensation step in multi-stage thiazole cycle-forming syntheses

    Final product types

    • Active Pharmaceutical Ingredients (e.g., anti-tubercular thiazoles)
    • Clinical trial intermediates for neuroprotective drugs

    2. Agrochemical Active Ingredient Precursor

    In crop protection manufacturing, this material acts as a building block for producing targeted fungicides and herbicides featuring thiazole or thiophene moieties. Its selectivity in hydrazide-based coupling reactions enables synthesis of high-purity actives with documented field stability. Compliance with agrochemical standards focuses on minimizing trace residuals and supporting dossier submission for new product registrations. Precise dosage depends on intended molecular transformations within the downstream synthesis.

    Industry compliance standards

    • FAO/WHO Specifications and Evaluations for Agricultural Pesticides
    • EPA 40 CFR Part 158 for registration data requirements
    • ISO 9001:2015 for raw material traceability
    • REACH Regulation EC No 1907/2006

    Typical usage ratio

    • 3–12% by weight in targeted condensation or cyclization steps, tailored based on desired active content and impurity profile

    Downstream process integration

    • Added post-halogenation or pre-acylation in controlled synthesis sequences for new molecule generation

    Final product types

    • Selective herbicides for cereal and broadleaf applications
    • Novel thiazole-based fungicides registered under national crop protection catalogs

    3. Specialty Dye and Pigment Intermediate

    Manufacturers in the specialty colorant sector utilize this compound as a nucleophile for creating sulfur- and heterocycle-containing dyes. Its participation in diazo coupling or Schiff base reactions allows fine-tuning of chromophore properties, especially for applications requiring high lightfastness or resistance to acid/base fading. Each production lot passes batch-specific purity and trace metal testing, aligned with the stringent requirements of advanced colorant applications.

    Industry compliance standards

    • ISO 105-A02/A05 for color fastness testing
    • Oeko-Tex® Standard 100 for restricted substances
    • REACH SVHC content constraints
    • EN 71-3 (for safety in toy colorants)

    Typical usage ratio

    • 0.5–2.5 molar equivalents relative to main dye arylamines or aldehydes, adjusted by color profile target

    Downstream process integration

    • Incorporated during diazotization or hydrazone formation stages in batch dye synthesis tanks

    Final product types

    • High-purity disperse dyes for polyester fibers
    • Metal-complex pigments used in automotive and high-performance coatings

    4. Analytical Reagent Manufacturing

    Laboratory and industrial test kit suppliers specify this hydrazide derivative as a calibrated reagent for colorimetric detection of aldehydes and ketones. Its reactive hydrazide group enables selective derivatization protocols in both environmental and clinical assay kits. Thorough documentation of batch homogeneity and impurity profile is mandatory for analytical approvals, due to quantification demands and inter-lab reproducibility standards at regulated laboratories worldwide.

    Industry compliance standards

    • ISO/IEC 17025 for chemical reference material suppliers
    • Ph. Eur. monograph for reagents (4th Ed.)
    • USP Analytical Reagents certification for trace analysis
    • OECD GLP (Good Laboratory Practice) for consistent reagent quality

    Typical usage ratio

    • 0.01–0.2 mol/L in ready-to-use analytical solutions; concentration selected per detection limit and assay protocol specifications

    Downstream process integration

    • Directly dissolved or stabilized in pre-packed diagnostic vials or assay kit immobilization cartridges

    Final product types

    • Certified aldehyde detection kits for air and water quality monitoring
    • Clinical diagnostic test kits for urinary ketone quantification
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