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Thiazole-4-Carboxaldehyde

    • Product Name Thiazole-4-Carboxaldehyde
    • Alias 4-Formylthiazole
    • Einecs 629-883-5
    • 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

    958924

    Chemical Name Thiazole-4-carboxaldehyde
    Cas Number 2717-57-9
    Molecular Formula C4H3NOS
    Molecular Weight 113.14 g/mol
    Appearance Yellow to brown crystalline powder
    Melting Point 60-63 °C
    Boiling Point 137-139 °C at 18 mmHg
    Density 1.315 g/cm³
    Solubility Soluble in ethanol and DMSO
    Purity Typically ≥ 97% (varies by supplier)
    Smiles C1=CSC(=N1)C=O
    Inchi InChI=1S/C4H3NOS/c6-2-4-3-7-1-5-4/h1-3H
    Refractive Index 1.655 (calculated)
    Storage Conditions Store at 2-8 °C, protect from light
    Synonyms 4-Formylthiazole

    As an accredited Thiazole-4-Carboxaldehyde factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Thiazole-4-Carboxaldehyde, 25g, is packaged in a sealed amber glass bottle with a clear product label for safety and identification.
    Shipping Thiazole-4-Carboxaldehyde is shipped in tightly sealed containers under dry, cool conditions, compliant with chemical handling regulations. Packaging is designed to prevent moisture and light exposure. The product is labeled with hazard information and shipped as a chemical substance, following relevant safety and transportation guidelines for laboratory or industrial use.
    Storage Thiazole-4-Carboxaldehyde should be stored in a tightly sealed container, protected from light and moisture, in a cool, dry, and well-ventilated area. Keep away from incompatible substances such as oxidizing agents. Store at room temperature or as specified on the manufacturer’s label. Ensure proper labeling and handle with appropriate personal protective equipment to avoid exposure.
    Application of Thiazole-4-Carboxaldehyde

    Applications of Thiazole-4-Carboxaldehyde in Industrial Manufacturing

    As a bulk producer of Thiazole-4-Carboxaldehyde, we supply a material built for complex, high-value synthesis routes across specialty chemicals sectors. This highly functional heterocyclic aldehyde supports multiple advanced applications where precision in purity, consistent quality, and industrial scalability define project success. Below we outline key industrial manufacturing scenarios deploying this raw material and detail relevant compliance, formulation, process, and end-product specifics for each downstream route.

    1. Active Pharmaceutical Ingredient (API) Intermediate Synthesis

    Pharmaceutical manufacturers utilize Thiazole-4-Carboxaldehyde as a critical intermediate in constructing thiazole-based active pharmaceutical ingredient cores, particularly for anti-infective and CNS compound classes. Its introduction occurs during targeted condensation or cyclization reactions in multi-step synthetic routes, supporting exacting requirements for impurity control and traceability from synthesis to finished dosage forms. Our material meets strict QC validation to enable qualification in GMP-regulated pharmaceutical synthesis chains.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice Guidance for Active Pharmaceutical Ingredients
    • USP–NF (United States Pharmacopeia–National Formulary) standards for intermediates
    • EU EudraLex Volume 4 GMP guidelines
    • APIC (Active Pharmaceutical Ingredient Committee) guidelines for supply chain transparency

    Typical usage ratio

    • Usage typically 0.1–0.4 molar equivalents relative to target API batch size; adjusted according to the number of synthetic steps, target impurity profile, and resin loading in solid-phase synthesis scenarios.

    Downstream process integration

    • Enters synthesis during early or mid-stage intermediate building block formation; charged directly to reactors for condensation with amines or coupling with carboxylic acids before purification and further reaction.

    Final product types

    • Anti-infective drug intermediates such as thiazolecephalosporins
    • CNS-active molecules incorporating thiazole scaffolds
    • Custom oncology APIs containing thiazole motif
    • Generic drugs with thiazole ring system

    2. Agrochemical Synthesis (Fungicides & Herbicides)

    Several leading agrochemical companies source Thiazole-4-Carboxaldehyde to prepare bioactive thiazole and thiazolidinone derivatives for crop protection agents. Formulators value its role in key cyclization processes and as a nucleophilic aldehyde fragment, enabled by precise control of batch contaminants that can disrupt downstream biological efficacy. Material handling aligns with industrial environmental and worker safety mandates, supporting large-scale field application products.

    Industry compliance standards

    • FAO/WHO Specifications and Evaluations for Agricultural Pesticides
    • REACH (EC 1907/2006) registration as intermediate for plant protection products
    • ISO 9001:2015 certified supply chains
    • GLP (Good Laboratory Practice) for product development data

    Typical usage ratio

    • Usually applied at 0.05–0.2 molar equivalents per step in batch synthesis, with adjustments for desired product selectivity and to minimize process waste in conversion to target actives.

    Downstream process integration

    • Charged at the condensation or ring-forming stage to form thiazole-functionalized agrochemical actives; integration with catalytic dehydration or halogenation steps depending on final molecule.

    Final product types

    • Fungicides based on thiazole moieties (e.g., thifluzamide, flutriafol derivatives)
    • Pre- and post-emergent herbicides containing thiazole linkage
    • Seed treatment actives incorporating thiazole intermediates
    • Combination crop protection formulations with synergist additives

    3. Dye and Pigment Manufacturing

    Dye and specialty pigment producers use Thiazole-4-Carboxaldehyde for synthesizing thiazole-based chromophores, particularly yellow and orange shades with enhanced lightfastness and solvent resistance required for textiles and polymer coloration. Process engineers incorporate the aldehyde in controlled condensation reactions with aromatic amines and sulfonic acids, ensuring downstream purity for high-performance finished pigments.

    Industry compliance standards

    • OEKO-TEX® Standard 100 for textile dye raw materials
    • REACH Annex XVII (Substances of Very High Concern restriction for dyes and pigments)
    • ISO 9001:2015 quality management for pigment batch traceability
    • ZDHC (Zero Discharge of Hazardous Chemicals) guidelines for formulated colorants

    Typical usage ratio

    • Added at 3–10% weight-to-weight basis relative to total reactive monomers for most synthetic dye processes; actual proportion may shift with target absorption spectrum and batch size.

    Downstream process integration

    • Introduced at the first stage of pigment core assembly; reacts with electron-donating groups during multi-step synthesis to produce water-soluble or solvent-stable thiazole dyes.

    Final product types

    • Disperse dyes for polyester and acetate fibers
    • Pigments for printing inks on packaging films
    • Sulfonated dyes for wool, nylon, and silk textiles
    • High-performance pigment dispersions for plastics

    4. Photographic Chemical Production

    Manufacturers of photographic chemicals and imaging developers use Thiazole-4-Carboxaldehyde as a key building block in preparing complex silver halide stabilizers and couplers. The compound fits into precise reactivity windows for assembling heterocyclic developer molecules, where impurity-sensitive integration into bulk formulations ensures consistent photographic quality. These applications demand compliance with environmental and consumer product safety standards for downstream photographic use.

    Industry compliance standards

    • RoHS (Restriction of Hazardous Substances) for finished imaging chemicals
    • REACH registration for photographic industry intermediates
    • General chemical safety regulations according to ISO 14001:2015
    • National Standards (GB/T for China, ASTM for USA) relevant to photochemistry

    Typical usage ratio

    • Usually applied at 0.1–0.5 molar equivalents per developer synthesis batch, modulated by product line (e.g., X-ray, microfilm, industrial vs. consumer photographic); chemical purity tightly controlled at each stage.

    Downstream process integration

    • Added during core developer assembly for condensation with substituted anilines or coupling agents; becomes an integral part of the small molecule infrastructure of the developer formulation.

    Final product types

    • Photographic developers and color couplers
    • Stabilizers for silver halide photo paper
    • Film processing chemicals for industrial and medical imaging
    • Monomeric color formers for color negative and reversal films

    5. Specialty Organic Synthesis (Electronic Materials)

    Producers of functional organic semiconductors and electronic chemicals employ Thiazole-4-Carboxaldehyde for the synthesis of advanced materials such as thiazole-functionalized oligomers, which are foundational in organic light-emitting diodes (OLEDs) and organic photovoltaics. The aldehyde’s selective reactivity enables formation of conjugated structures with controlled energy levels, supporting device manufacturers' tight specifications for purity and performance. Material traceability and contamination avoidance are critical in this advanced downstream context.

    Industry compliance standards

    • ISO 9001:2015 certified manufacturing and supply protocols for electronics chemicals
    • REACH compliance for organic conductive materials
    • RoHS directives, particularly for substances in electronic display materials
    • VDE (Verband der Elektrotechnik) standards for functionally relevant chemical impurities

    Typical usage ratio

    • Usually 0.02–0.15 molar equivalents per synthesis step, tailored to target molecular weight of oligomer or polymer and adjusted based on finished device specification (emission wavelength, electrical conductivity).

    Downstream process integration

    • Reacted at initial monomer synthesis and at subsequent chain extension or cross-linking steps in polymer backbone formation; aligned with solvent and purity demands of thin-film device fabrication.

    Final product types

    • Organic semiconductors for OLED displays and lighting panels
    • Small molecule donors for organic photovoltaic cells
    • Photoconductive layers for electrophotography and sensors
    • Electroluminescent materials for flexible electronics
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