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1-(5-Tert-Butyl-1,3,4-Thiadiazol-2-Yl)-1,3-Dimethylurea

    • Product Name 1-(5-Tert-Butyl-1,3,4-Thiadiazol-2-Yl)-1,3-Dimethylurea
    • Alias Thidiazuron
    • Einecs EINECS 410-240-7
    • 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

    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 & Storage
    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.
    Application of 1-(5-Tert-Butyl-1,3,4-Thiadiazol-2-Yl)-1,3-Dimethylurea

    Applications of 1-(5-Tert-Butyl-1,3,4-Thiadiazol-2-Yl)-1,3-Dimethylurea in Industrial Manufacturing

    1-(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 Protection

    Agrochemical 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

    • FAO/WHO Specifications for Plant Protection Products
    • ISO 9001:2015-certified QC processes
    • EU Regulation (EC) No 1107/2009 for pesticide products
    • REACH Annex IV-IX dossier requirements

    Typical usage ratio

    • Raw material included at 15–28% by weight in concentrated actives mass, adjusted based on target active substance output and solubility profile.

    Downstream process integration

    • Introduced immediately post-halogenation of aromatic amines; reaction temperature maintained at 75–90°C, inert gas blanketed.

    Final product types

    • Systemic fungicide formulations—wettable granules, suspension concentrates (SC), and water dispersible granules (WDG) for field application.

    2. Intermediate in Synthesis of Lubricant Additives for Engine Oils

    Industrial 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

    • API SN/CF Additive Compatibility Protocols
    • SAE J183 and ASTM D4485 Engine Oil Standards
    • ISO/TS 16949 automotive manufacturing system
    • Global Lubricant Quality Assessment System (GLQAS)

    Typical usage ratio

    • 0.5–2.3% by total package mass, scaled according to base oil polarity and additive multidose system design.

    Downstream process integration

    • Charged to blending vessels post-alkenyl succinimide mixing, followed by heat integration at 115–135°C with continuous monitoring for nitrogen content.

    Final product types

    • High-performance crankcase engine oils, heavy-duty diesel blends, and industrial hydraulic fluids with anti-wear specifications.

    3. Active Ingredient for Seed Treatment Coatings

    Seed 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

    • OECD Seed Treatment Safety Assessment Module
    • EPA 40 CFR Part 180 (Pesticide Residue Tolerances)
    • GMP+ FSA B2 standards for feed safety
    • ISO 17025 laboratory verification

    Typical usage ratio

    • 1.5–5% of total coating formulation by weight; level optimized according to seed type, coating thickness, and local maximum residue limits.

    Downstream process integration

    • Injected in aqueous pre-polymer core mixing vessels prior to pigment and plasticizer addition; temperature maintained under 50°C to ensure uniform dispersion.

    Final product types

    • Treated corn, soybean, wheat, and canola seeds with shelf-stable coating for commercial planting sectors.

    4. Modifier in Industrial Water Treatment Biocidal Blends

    Large-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

    • ANSI/AWWA B451 Disinfectant Standards
    • EN 1276—Chemical Disinfectants (Industrial Requirements)
    • OECD 209 Activated Sludge Biodegradation Test
    • EMEA 400 Microbial Quality on Process Water

    Typical usage ratio

    • 0.3–1.2% by final product weight, titrated based on system volume, microbial load, and retention time.

    Downstream process integration

    • Added at the final formulation stage after primary active blend, under agitation at ambient temperature, with conductivity monitored to confirm dispersion completeness.

    Final product types

    • Industrial water biocide concentrates, closed-circuit cooling water treatment blends, and recirculating loop biofilm inhibitors.
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