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Ethyl 4-Methyl-1,2,3-Thiadiazole-5-Carboxylate

    • Product Name Ethyl 4-Methyl-1,2,3-Thiadiazole-5-Carboxylate
    • Alias Ethyl 4-methyl-5-carboethoxy-1,2,3-thiadiazole
    • Einecs 400-480-3
    • 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

    324689

    Chemicalname Ethyl 4-Methyl-1,2,3-Thiadiazole-5-Carboxylate
    Casnumber 356783-16-9
    Molecularformula C6H8N2O2S
    Molecularweight 172.20 g/mol
    Appearance White to off-white solid
    Solubility Soluble in organic solvents
    Purity Typically >98%
    Smiles CCOC(=O)c1nnc(s1)C
    Inchi InChI=1S/C6H8N2O2S/c1-3-10-6(9)5-4(2)8-7-11-5/h3H2,1-2H3
    Storagetemperature 2-8°C

    As an accredited Ethyl 4-Methyl-1,2,3-Thiadiazole-5-Carboxylate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The product is packaged in a 25-gram amber glass bottle with a secure screw cap, labeled with chemical details and safety information.
    Shipping Ethyl 4-Methyl-1,2,3-Thiadiazole-5-Carboxylate should be shipped in tightly sealed containers, protected from moisture, heat, and direct sunlight. Handle as a potentially hazardous chemical, ensuring proper labeling and documentation. Follow all applicable regulations for transport, using UN-approved packaging if required. Suitable for ground or air shipment by qualified carriers.
    Storage Ethyl 4-Methyl-1,2,3-Thiadiazole-5-Carboxylate should be stored in a tightly sealed container, away from moisture, light, and incompatible substances, such as strong oxidizing agents. It should be kept in a cool, dry, and well-ventilated area, preferably at room temperature or as indicated by the manufacturer. Proper labeling and secondary containment are recommended to prevent spills and accidental exposure.
    Application of Ethyl 4-Methyl-1,2,3-Thiadiazole-5-Carboxylate

    Applications of Ethyl 4-Methyl-1,2,3-Thiadiazole-5-Carboxylate in Industrial Manufacturing

    Ethyl 4-Methyl-1,2,3-Thiadiazole-5-Carboxylate delivers targeted functional properties in several technically advanced industrial sectors. Our manufacturing experience ensures consistent quality for demanding downstream processes requiring tight compliance and reliable performance. Below are the primary, field-proven application segments using our raw material as a critical component in differentiated industrial production flows.

    1. Pharmaceutical Intermediate for Thiadiazole-Based Drug Synthesis

    API manufacturers frequently select this compound as a building block in multi-step synthesis routes for novel thiadiazole pharmaceuticals, including antimicrobial, anticonvulsant, and anti-inflammatory agents where heterocycle frameworks are core moieties. Downstream formulators rely on established reactivity profiles and clear impurity management when using this chemical in pilot and commercial scale-up, especially for regulatory submissions in global markets.

    Industry compliance standards

    • ICH Q7 GMP for Active Pharmaceutical Ingredients
    • USP-NF and European Pharmacopoeia monograph traceability (as applicable to downstream intermediates)
    • FDA 21 CFR Part 211 Good Manufacturing Practice
    • EDQM CEP certification requirements (for exported APIs)

    Typical usage ratio

    • 10–25 mol% relative to target pharmaceutical core—determined by final dosage synthesis and route optimization; ratios subject to API pathway and regulatory validation batch design

    Downstream process integration

    • Introduced as a key heterocyclic reactant during condensation or cyclization steps after primary scaffold assembly
    • Participates in amidation, esterification, or nucleophilic substitution reactions within batch reactor or flow chemistry equipment

    Final product types

    • Pharmaceutical active intermediates for anti-infective drugs
    • Branded and generic finished pharmaceutical ingredients (API) using thiadiazole cores
    • Pilot batches for NDA, ANDA, or DMF submissions

    2. Agrochemical Synthesis for Crop Protection Agents

    Chemical crop protection developers use our product as a core thiadiazole building block in herbicide and fungicide research, formulating selective agents through controlled modifications of this structure. Process chemists integrate this raw material in pilot and scale production to achieve regulatory-compliant impurity profiles and reproducible biological activities, controlling micro-contaminant thresholds throughout the synthesis workflow as required by government registrations.

    Industry compliance standards

    • FAO/WHO specifications for pesticide technical material
    • OECD GLP (Good Laboratory Practice) for regulatory studies
    • REACH registration for European market access
    • ISO 9001:2015 certified quality management systems (for bulk agrochemicals)

    Typical usage ratio

    • 5–18% by weight in reaction charge—specific ratio optimized according to target active molecule yield and desired selectivity; pre-formulation screening may adjust range

    Downstream process integration

    • Fed as a starting reagent in synthesis reactors during stepwise assembly of thiadiazole-linked pesticide or fungicide actives
    • Blended in solvent-based or aqueous-phase batch synthesis with subsequent crystallization, filtration, and purification

    Final product types

    • Technical concentrate herbicides and fungicides with thiadiazole substructures
    • Registered crop protection actives supplied to formulators
    • Granular and EC (emulsifiable concentrate) pesticide products

    3. Specialty Chemical Intermediate for Polymer Additives

    Engineering resin producers and specialty additive suppliers apply this molecule as a nucleating or stabilizing intermediate in the synthesis of functional thiadiazole derivatives designed to boost UV resistance or oxidation stability of plastics and specialty coatings. The chemical structure supports targeted functionalization, allowing downstream customers to formulate polymer masterbatches meeting high-performance end-product criteria required by automotive, electronics, and construction sectors.

    Industry compliance standards

    • RoHS Directive for electronics applications
    • EN 71-3 (Safety of Toys) for polymeric additive compliance
    • REACH (EU Regulation No 1907/2006) registration
    • ISO 14001 Environmental Management (for sustainable supply chains)

    Typical usage ratio

    • 0.1–2.5% by weight in pre-polymer additive batches—proportion determined by polymer type, degree of protection required, and downstream extrusion parameters

    Downstream process integration

    • Introduced into synthesis of thiadiazole-class stabilizers via esterification or ring-opening reactions prior to compounding
    • Blended into masterbatch additives, then incorporated into thermoplastic or thermoset resin blending lines

    Final product types

    • UV-stabilizing and antioxidant polymer additives for PE, PP, PVC, ABS, or polyurethane matrices
    • High-durability engineering plastics for automotive interiors
    • Electronics-compatible flame-retardant polymers

    4. Intermediate for Advanced Dye and Pigment Synthesis

    Colorant manufacturers leverage the specific reactivity of this thiadiazole ester to construct specialty azo and heterocyclic dyes used in professional textile, plastic, and inkjet colorant applications. Its utility in fine tuning hue and fastness properties has established this material as a preferred intermediate for downstream chromophore assembly, enabling adaptation to both water-based and solvent-based pigment manufacturing lines while maintaining strict impurity control for application-critical specifications.

    Industry compliance standards

    • OEKO-TEX Standard 100 (product class safety for textiles)
    • EN 71-7 (safety of finger paints and colorants)
    • REACH Annex XVII and SVHC restrictions (non-listed for use in pigments)
    • ISO 9001 verified quality management for synthetic dyes

    Typical usage ratio

    • 0.5–8% by weight per pigment batch—adjusted based on color shade depth, dispersion stability requirements, and downstream blending needs

    Downstream process integration

    • Loaded as a condensation or coupling reactant during batch dye synthesis or pigment salt formation step
    • Incorporated ahead of granulation, spray-drying, or milling in pigment manufacturing lines

    Final product types

    • Synthetic organic dyes for textile and leather application
    • High-performance pigments for plastics and coatings
    • Water- and solvent-based inkjet colorant dispersions
    Free Quote

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