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HS Code |
573921 |
| Iupac Name | 2-Amino-5-(4-methoxyphenyl)-1,3,4-thiadiazole |
| Molecular Formula | C9H9N3OS |
| Molecular Weight | 207.26 g/mol |
| Appearance | Solid |
| Melting Point | 162-165°C |
| Cas Number | 34650-67-2 |
| Solubility | Slightly soluble in water, soluble in organic solvents |
| Smiles | COC1=CC=C(C=C1)C2=NN=C(N2)N |
| Pubchem Cid | 179581 |
| Storage Conditions | Store in a cool, dry place, tightly closed container |
As an accredited 2-Amino-5-(4-Methoxyphenyl)-1,3,4-Thiadiazole factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | White HDPE bottle containing 25 grams of 2-Amino-5-(4-Methoxyphenyl)-1,3,4-Thiadiazole, securely sealed with tamper-evident cap. |
| Shipping | 2-Amino-5-(4-Methoxyphenyl)-1,3,4-Thiadiazole is shipped in tightly sealed containers, protected from moisture, light, and extreme temperatures. Packaging complies with applicable chemical transport regulations, ensuring safe transit. Handle with care, using appropriate personal protective equipment. Shipping documentation includes safety and handling instructions in accordance with local and international guidelines. |
| Storage | Store 2-Amino-5-(4-methoxyphenyl)-1,3,4-thiadiazole in a tightly sealed container in a cool, dry, and well-ventilated area, away from sources of heat, ignition, and incompatible materials such as strong oxidizing agents. Protect from moisture and direct sunlight. Ensure containers are clearly labeled. Follow appropriate laboratory safety protocols, including use of gloves, eye protection, and proper disposal procedures for chemical waste. |
Applications of 2-Amino-5-(4-Methoxyphenyl)-1,3,4-Thiadiazole in Industrial Manufacturing2-Amino-5-(4-Methoxyphenyl)-1,3,4-Thiadiazole supports specialized synthesis processes for advanced industries, including pharmaceuticals, agricultural chemicals, polymer additives, and dye intermediates. As a direct manufacturer, we provide this material with batch-level traceability to downstream processors integrating it into carefully controlled environments. 1. Pharmaceutical Intermediate for Antimicrobial Active IngredientsThis compound serves as a critical building block in the synthesis of antimicrobial pharmaceutical agents, especially in cephalosporin and related heterocyclic drugs. Research-driven organizations incorporate it during multi-step active ingredient synthesis to introduce thioazole rings, which are valued for improving biological activity. The manufacturing process often involves acylation or condensation reactions under controlled temperatures and inert atmospheric conditions, with stringent solubility and impurity thresholds to meet regulatory pharmacopoeia requirements. Industry compliance standards
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2. Synthesis of Herbicide and Fungicide Active ComponentsAgrochemical formulators utilize the thiadiazole framework to provide selectivity and environmental stability in new-generation herbicides and fungicides. Incorporated through condensation reactions, this material contributes nitrogen and sulfur donors, enhancing the efficacy and regulatory acceptability of final agro-products. Integration occurs under closed systems monitored for solvent residue and thermal stability per ISO and FAO requirements. Industry compliance standards
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3. Specialty Additive in Engineering PolymersWithin the engineering polymer sector, processors employ this compound as a nucleating and stabilizing agent in specialty resin systems, such as polyamides and polyesters, to improve crystallinity and heat resistance. Controlled addition during polymer melt processing ensures uniform dispersion and prevents polymer decomposition. Stringent QC checks ensure compliance with materials safety and functional performance protocols set by automotive and consumer electronics end-users. Industry compliance standards
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4. Dye Intermediate for Azo and Disperse ColorantsTextile and pigment manufacturers value this compound as a diazo component precursor in the synthesis of disperse and azo dyes, providing enhanced color fastness and unique chromatic properties. It participates in diazotization and coupling reactions at controlled temperatures and pH levels, resulting in stable intermediates suitable for integration into synthetic fiber dyeing. Process control focuses on removing trace mineral impurities and confirming amine content for consistency in shade and application performance. Industry compliance standards
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