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Thiazole

    • Product Name Thiazole
    • Alias Thiazole
    • Einecs 204-819-1
    • 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

    448747

    Chemicalname Thiazole
    Molecularformula C3H3NS
    Molarmass 85.12 g/mol
    Casnumber 288-47-1
    Appearance Colorless to pale yellow liquid
    Boilingpoint 116 °C
    Meltingpoint -30 °C
    Density 1.107 g/cm³
    Solubilityinwater Soluble
    Odor Pyridine-like, unpleasant
    Refractiveindex 1.527
    Flashpoint 19 °C (closed cup)
    Pubchemcid 9273

    As an accredited Thiazole factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing A 500g amber glass bottle labeled "Thiazole," featuring hazard symbols, CAS number, batch details, and tightly sealed with a screw cap.
    Shipping Thiazole is typically shipped in tightly sealed containers, protected from light and moisture, and stored in a cool, well-ventilated area. It is classified as a hazardous material, so shipping must comply with relevant regulations, including appropriate labeling, documentation, and handling precautions to prevent exposure, leaks, or accidental release during transit.
    Storage Thiazole should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizers. Keep the container away from direct sunlight, moisture, and heat. Proper labeling and secondary containment are recommended to prevent leaks, spills, or accidental exposure. Store under inert atmosphere if required by safety guidelines.
    Application of Thiazole

    Applications of Thiazole in Industrial Manufacturing

    Thiazole derivatives occupy a crucial role in specialized industrial supply chains. From agrochemical formulations to the pharmaceutical sector, our thiazole intermediates support stringent regulations, precise process control, and critical end-use requirements. Below we outline the established downstream application scenarios, their compliance frameworks, formulation practices, process integration, and finished product outputs.

    1. Pharmaceutical Active Ingredient Synthesis

    Thiazole compounds serve as key building blocks in the synthesis of several pharmaceutical actives, particularly in anti-infective and central nervous system drugs. Formulators rely on thiazole moieties for structural frameworks during multi-step reaction schemes, where the purity and trace impurity levels of the starting material directly influence API quality. Each production batch must trace regulatory origin and document full traceability for regulatory submissions.

    Industry compliance standards

    • Current Good Manufacturing Practice (cGMP, 21 CFR parts 210/211)
    • International Council for Harmonisation (ICH Q7, Q3A/B)
    • European Pharmacopoeia (Ph. Eur.)/United States Pharmacopeia (USP)
    • REACH Registration and Compliance (EU regulations)

    Typical usage ratio

    • In API synthesis, thiazole intermediates commonly range from 0.5 mol% to 2.0 mol% relative to final API mass, adjusted based on pathway yield and impurity control requirements.

    Downstream process integration

    • Introduced during early or mid-stage synthetic reactions (cyclization or condensation steps), often under controlled temperature and pH, followed by isolation, purification, and further derivatization to generate the drug molecule backbone.

    Final product types

    • Antibiotics (e.g., cephalosporins)
    • Antifungal agents containing thiazole rings
    • Central nervous system APIs (e.g., anticonvulsants)
    • Intermediate precursors for other regulated pharmaceuticals

    2. Crop Protection Active Ingredient Manufacturing

    Agrochemical producers apply thiazole intermediates extensively in the creation of triazole fungicides and insecticidal agents. Control over impurity profiles and batch reproducibility is essential, since thiazole structures impart both efficacy and selectivity to the final actives. Downstream partners evaluate compliance with global residue and toxicity limits, often requesting full synthetic origin disclosure and documentation of raw material procurement.

    Industry compliance standards

    • FAO/WHO Pesticide Specifications
    • OECD Good Laboratory Practice (GLP)
    • EPA Federal Insecticide, Fungicide, and Rodenticide Act (FIFRA)
    • China GB Farm Chemical Product Standards

    Typical usage ratio

    • Generally 1.0–3.0% by weight in initial reaction blends, adjusted by the desired crop protection agent structure or according to pilot-scale balance between efficacy and end-residue tolerances.

    Downstream process integration

    • Added during heterocyclization reactions to form the thiazole ring, or as a backbone unit for triazole-cyclization in custom synthesis of pesticide actives; subsequent purification and formulation blending yields technical concentrate.

    Final product types

    • Fungicide technical powders and suspensions (e.g., prothioconazole, flusilazole)
    • Insecticidal agent intermediates
    • Pesticide formulation concentrates
    • Seed dressing agents containing thiazole nuclei

    3. Dye and Pigment Intermediates Production

    Synthetic dye manufacturers source thiazole derivatives for the production of azo and sulfur dyes, especially for applications demanding bright yellow to orange color shades and improved lightfastness on textile fibers. Stringent batch-to-batch colorimetric consistency and minimal metal residues are prioritized to comply with final textile export regulations and azo restriction lists.

    Industry compliance standards

    • Oeko-Tex® Standard 100, Annex 4 (chemical substances and banned colorants)
    • ZDHC MRSL (Zero Discharge of Hazardous Chemicals Manufacturing Restricted Substances List)
    • EU REACH Annex XVII Dye Restrictions
    • ISO 105 Series Color Fastness Tests

    Typical usage ratio

    • Ranges from 0.8% to 5% by weight of reaction mixture, dictated by target pigment strength and dye shade depth; fine-tuned in process development trials for shade accuracy.

    Downstream process integration

    • Reacted with diazonium or sulfone intermediates under regulated temperature and pH to achieve ring closure or azo coupling; thiazole acts as nucleophile or color moiety donor; process monitoring for color stability and sulfonate yield is pivotal.

    Final product types

    • Sulfur-based textile dyes
    • Azo dyes for cotton or blended fabrics
    • Specialty pigments for inks or paints
    • Color concentrates for plastic masterbatches

    4. Rubber Chemical Accelerator Synthesis

    In technical rubber processing, thiazole-based accelerators are fundamental in controlling the vulcanization rate of natural and synthetic rubber. Tire and industrial rubber component makers demand narrow purity specifications and traceability documentation, as batch consistency in accelerator input directly affects cross-link density and mechanical strength of the final cured elastomer. All downstream recipes comply with global automotive and safety critical material standards.

    Industry compliance standards

    • ISO 9001 Certified Quality Systems
    • ASTM D2000 Rubber Properties Standards
    • EU Directive 2000/53/EC (End-of-life Vehicles; hazardous substance limits)
    • GB/T 19229-2015 (China Rubber Accelerator Requirements)

    Typical usage ratio

    • Normally 0.5 phr to 1.5 phr (parts per hundred rubber) in total formulation, adapted based on cure kinetics under laboratory rheometry trials and physical test results for modulus or elongation.

    Downstream process integration

    • Blended into the compounding phase alongside fillers, sulfur, and processing oils; dispersion ensures reaction with sulfur donors during compression molding or extruding at high temperatures, after which final vulcanization sets the desired network structure.

    Final product types

    • Automotive tires (truck, passenger, specialty)
    • Conveyor belts and industrial sheetings
    • Sealing gaskets and isolation mounts
    • General-purpose mechanical rubber goods

    5. Flavor and Fragrance Intermediate Sourcing

    Food and aroma ingredient manufacturers use specific thiazole derivatives to generate key flavor and odor notes, such as roasted or meaty nuances, in complex formulations meant for the food and beverage sector. All thiazole building blocks must trace food-grade origins, conform to toxicological safety evaluations, and support both halal and kosher certification workflows when deployed in compliance as regulated additives or process flavors.

    Industry compliance standards

    • FCC (Food Chemicals Codex) Specification
    • JECFA (Joint FAO/WHO Expert Committee on Food Additives) Evaluations
    • EU Food Flavouring Regulation (EC No 1334/2008)
    • Kosher/Halal Auditing (where applicable)

    Typical usage ratio

    • 0.01% to 0.2% by weight in finished flavor base, evaluated in sensory prototype runs, with adjustments based on consumer panel feedback and regulatory flavor threshold guidelines.

    Downstream process integration

    • Reacted as intermediate or finished molecule during flavor concentrate blending, subjected to steam distillation and solvent recovery steps to remove unwanted volatiles; introduced at either compounding or spray-drying stages according to stability profiling.

    Final product types

    • Roasted and meaty flavor enhancers for snacks and ready meals
    • Beverage flavor bases
    • Processed food savory blends
    • Fragrance ingredient concentrates for perfumery
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