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4-Methylthiazole-5-Carboxaldehyde

    • Product Name 4-Methylthiazole-5-Carboxaldehyde
    • Alias 4-Methyl-1,3-thiazole-5-carbaldehyde
    • Einecs EINECS 266-543-9
    • 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

    967347

    Chemical Name 4-Methylthiazole-5-Carboxaldehyde
    Cas Number 63450-73-7
    Molecular Formula C5H5NOS
    Molecular Weight 127.16 g/mol
    Appearance Light yellow to brown crystalline powder
    Melting Point 77-80°C
    Boiling Point No data available
    Density No data available
    Purity Typically ≥98%
    Solubility Soluble in polar organic solvents (e.g., DMSO, methanol)
    Smiles CC1=NC=C(S1)C=O
    Inchi InChI=1S/C5H5NOS/c1-4-6-2-5(3-7)8-4/h2-3H,1H3
    Storage Conditions Store at 2-8°C, in a tightly closed container
    Safety Hazards May cause skin and eye irritation
    Refractive Index No data available

    As an accredited 4-Methylthiazole-5-Carboxaldehyde factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle containing 25 grams of 4-Methylthiazole-5-Carboxaldehyde, sealed with a tamper-evident cap and labeled with hazard warnings.
    Shipping **Shipping Description:** 4-Methylthiazole-5-Carboxaldehyde is packed securely in sealed containers, protected from moisture and light. It is shipped as a laboratory chemical, typically under ambient conditions, with all regulations for hazardous chemicals followed. Appropriate labeling and documentation ensure safe transport, complying with international shipping standards and local chemical safety guidelines.
    Storage 4-Methylthiazole-5-carboxaldehyde should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from direct sunlight and incompatible materials such as strong oxidizing agents. Keep the storage temperature below room temperature if possible. Ensure proper labeling, and avoid exposure to heat, moisture, and ignition sources to maintain chemical stability and safety.
    Application of 4-Methylthiazole-5-Carboxaldehyde

    Applications of 4-Methylthiazole-5-Carboxaldehyde in Industrial Manufacturing

    As a dedicated chemical raw material manufacturer, we supply 4-Methylthiazole-5-Carboxaldehyde for specific industrial purposes where strict standards, defined formulation practices, and controlled processes are essential. Below, we detail the principal categories of application where this specialty compound plays a vital role in downstream manufacturing, with exclusive focus on sectors and processes validated by current industrial adoption.

    1. Pharmaceutical Intermediate for Thiazole-Derived API Synthesis

    4-Methylthiazole-5-Carboxaldehyde serves as a highly selective intermediate in the multi-step synthesis routes for active pharmaceutical ingredients (APIs) incorporating thiazole frameworks, such as antidiabetic agents and antimicrobial compounds. Downstream processors use this intermediate in controlled condensation and cyclization steps, crucial for ensuring batch consistency and meeting regulatory agency requirements for traceability and purity in pharmaceutical manufacturing.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • Current Good Manufacturing Practice in Manufacturing, Processing, Packing, or Holding of Drugs (US FDA 21 CFR Part 210/211)
    • European Pharmacopoeia monographs relevant to target APIs
    • Chinese Pharmacopoeia (ChP) for intermediates and APIs

    Typical usage ratio

    • 0.05 mol to 0.2 mol per mol of final API, adjustable based on API scaffold and reaction pathway design

    Downstream process integration

    • Introduced in the early condensation step, often after initial activation of core reagents; subjected to further functionalization or ring-closure during subsequent synthesis stages

    Final product types

    • Thiazole-based antidiabetic drugs (e.g., pioglitazone intermediates)
    • Broad-spectrum antimicrobial agents
    • Anti-inflammatory small molecule drugs
    • Synthetic intermediates for further contract API development

    2. Aroma Chemical Precursor in Flavors & Fragrances Manufacturing

    Industrial flavor and fragrance houses incorporate 4-Methylthiazole-5-Carboxaldehyde to introduce roasted, nutty, or meaty top notes into complex aroma blends. Its reactivity enables downstream processors to carry out controlled reductive amination and acylation, crafting high-impact flavor top notes that comply with end-use formulations for food, beverage, and perfume bases. The use of this intermediate demands strict adherence to purity and food safety standards in blending operations.

    Industry compliance standards

    • IFRA Code of Practice and Standards
    • US Food Additive Regulations (21 CFR Part 172)
    • Regulation (EC) No 1334/2008 on Flavourings and Certain Food Ingredients
    • ISO 9235 on aroma chemicals

    Typical usage ratio

    • 0.01% to 0.15% by weight within finished aroma concentrates; exact dosing adjusted for finished product volatility and customer preference

    Downstream process integration

    • Added during precursor blending and subjected to reductive amination or acetylation before final mixing and stabilization of the aroma concentrate

    Final product types

    • Compound flavors for food service applications
    • Ready-to-use beverage flavors (meat, roasted nut, savory blends)
    • Perfume and cologne base notes
    • Processed flavor enhancers for snack and seasoning industries

    3. Agrochemical Intermediate for Heterocyclic Pesticide Formulations

    Downstream agrochemical manufacturers employ 4-Methylthiazole-5-Carboxaldehyde as a precursor building block in the synthesis of advanced heterocyclic pesticide molecules. Its chemical properties facilitate the efficient construction of specific ring systems that enhance target specificity and environmental stability, while manufacturing lines maintain strict adherence to product stewardship and residue compliance according to national and international standards.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • Regulation (EC) No 1107/2009 concerning the placing of plant protection products on the market
    • China GB 2763 Maximum Residue Limits for Pesticides in Food
    • EPA Pesticide Registration (40 CFR Part 152)

    Typical usage ratio

    • 0.1 mol to 0.5 mol per mol of main active compound, scaled per synthesis method and active ingredient design

    Downstream process integration

    • Incorporated in the core condensation step to construct the key heterocyclic structure, followed by purification, formulation into technical material, and dilution for field application products

    Final product types

    • Heterocyclic fungicide molecules
    • Active insecticide compounds with thiazole motifs
    • Intermediate concentrates for export or direct formulation
    • Commercial plant protection products (EC, SC, WG)

    4. Advanced Material Synthesis for Functional Organic Coatings

    The specialty coatings sector integrates 4-Methylthiazole-5-Carboxaldehyde within synthesis routes for functionalized thiazole monomers, which become crosslinkable units in high-performance polymer matrices. Manufacturers use it at defined stages to impart desired physical and chemical resistance properties. Documentation and quality control must align with strict industrial and environmental standards for specialty polymers and high-end surface engineering.

    Industry compliance standards

    • REACH Regulation (EC) No 1907/2006 for registration and safe use
    • ISO 9001:2015 for Quality Management in Chemical Manufacturing
    • RoHS Directive 2011/65/EU, as relevant for end-use segments
    • ISO 14001:2015 for Environmental Management Systems

    Typical usage ratio

    • 0.5% to 3% by mass in monomer reaction blends; depends on desired crosslink density and target polymer properties

    Downstream process integration

    • Charged during thiazole monomer synthesis, then polymerized by copolymerization or grafting methods to produce functional coatings with specialized performance specifications

    Final product types

    • Corrosion-resistant polymer coatings
    • Functional adhesives for electronics assembly
    • Smart surface films with anti-static or anti-fouling features
    • High-durability industrial topcoats
    Free Quote

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