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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 | 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. |
Applications of Thiophene-3-Acetic Acid Hydrazide in Industrial ManufacturingThiophene-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 SynthesisThis 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
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2. Agrochemical Active Ingredient PrecursorIn 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
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3. Specialty Dye and Pigment IntermediateManufacturers 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
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4. Analytical Reagent ManufacturingLaboratory 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
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