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HS Code |
708355 |
| Chemical Name | 1-(5-Tert-Butyl-1,3,4-Thiadiazol-2-Yl)-1,3-Dimethylurea |
| Molecular Formula | C9H16N4OS |
| Molecular Weight | 228.32 g/mol |
| Cas Number | 51707-55-2 |
| Appearance | White to off-white solid |
| Melting Point | 183-185 °C |
| Solubility | Slightly soluble in water |
| Structure | Thiadiazole ring with tert-butyl and dimethylurea substituents |
| Iupac Name | 1,3-dimethyl-1-(5-tert-butyl-1,3,4-thiadiazol-2-yl)urea |
| Pubchem Cid | 2724443 |
| Smiles | CC(C)(C)c1nnc(n1)NC(=O)N(C)C |
| Storage Conditions | Store in a cool, dry place, tightly closed container |
As an accredited 1-(5-Tert-Butyl-1,3,4-Thiadiazol-2-Yl)-1,3-Dimethylurea factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | White, tightly sealed 25g amber glass bottle with safety cap; labeled with chemical name, purity, hazard symbols, and batch number. |
| Shipping | 1-(5-Tert-Butyl-1,3,4-Thiadiazol-2-Yl)-1,3-Dimethylurea is shipped in tightly sealed containers, protected from moisture, light, and extreme temperatures. Transport complies with applicable chemical safety regulations, including labeling and documentation. Ensure secure handling to prevent spills or exposure during transit. Consult the Safety Data Sheet (SDS) for specific shipping restrictions and hazard classifications. |
| Storage | Store **1-(5-tert-butyl-1,3,4-thiadiazol-2-yl)-1,3-dimethylurea** in a cool, dry, well-ventilated area, away from direct sunlight, heat sources, and incompatible substances such as strong oxidizers. Keep the container tightly closed when not in use. Use appropriate personal protective equipment when handling, and store in clearly labeled, corrosion-resistant containers to prevent contamination and degradation. |
Applications of 1-(5-Tert-Butyl-1,3,4-Thiadiazol-2-Yl)-1,3-Dimethylurea in Industrial Manufacturing1-(5-Tert-Butyl-1,3,4-Thiadiazol-2-Yl)-1,3-Dimethylurea functions as a specialized intermediate and additive in various targeted chemical industries. Below, we outline practical application fields based on verified industrial adoption, with detailed integration, compliance, and end-product outcomes. 1. Synthesis of Selective Systemic Fungicides for Crop ProtectionAgrochemical formulators use this compound as a precursory building block for triazole and thiadiazole-based systemic fungicides. The molecule’s thiadiazole core facilitates step-growth reactions with aromatic chlorides in protected atmospheres, improving active ingredient stability against hydrolysis. Manufacturers integrate this raw material at the condensation stage, following strict process control for moisture and residual solvent. The downstream formulation involves wet milling, stabilization with proprietary dispersants, and microencapsulation before packaging as wettable granules or SC concentrates. Industry compliance standards
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2. Intermediate in Synthesis of Lubricant Additives for Engine OilsIndustrial lubricant manufacturers employ this material as a sulfur–nitrogen moiety source in additive packages targeting wear and oxidation resistance enhancements. The molecule integrates during the blending of detergent-dispersant systems, reacting under controlled heat with polyalkylene succinimide intermediates. Accurate dosing counteracts unwanted nitrosamine formation. Post-reaction, blending proceeds in closed reactors under drying agents to achieve precise viscosity and color metrics before filtration into additive concentrates. Industry compliance standards
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3. Active Ingredient for Seed Treatment CoatingsSeed treatment specialists use this thiadiazole-urea derivative as an integral ingredient in protective polymer coatings to deliver targeted antifungal activity. The compound’s structure ensures low phytotoxicity and controlled leach rate on seed surfaces. Production lines incorporate this raw material in pre-mix tanks with acrylic latex polymers under pH control, followed by high-shear blending and in-line viscosity tuning. Final coating composition meets regulatory migratory residue caps and offers tailored film-forming properties for various seed species. Industry compliance standards
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4. Modifier in Industrial Water Treatment Biocidal BlendsLarge-scale water treatment operators include this compound as a performance boosting agent in blended biocidal programs. The active thiadiazole ring demonstrates enhanced chelation properties, disrupting microbial biofilm matrices in closed-loop and recirculating cooling systems. Operators introduce the material during the final blending of aqueous biocide concentrates, employing continuous agitation and pH adjustment to match plant specifications. The formulation process prioritizes compliance to discharge regulations and compatibility testing for co-treatments such as phosphonates. Industry compliance standards
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