Sourcing High-Purity 3-Acetyl-2,5-dichlorothiophene: A Guide for Buyers
In the intricate world of pharmaceutical development, the quality and purity of chemical intermediates are paramount. One such vital compound is 3-Acetyl-2,5-dichlorothiophene (CAS: 36157-40-1), a key building block used extensively in the synthesis of Active Pharmaceutical Ingredients (APIs). For procurement managers, R&D scientists, and formulation chemists, understanding the nuances of sourcing this chemical is crucial for successful project outcomes.
Understanding 3-Acetyl-2,5-dichlorothiophene
This heterocyclic organic compound, with the molecular formula C6H4Cl2OS, is characterized by its thiophene ring substituted with an acetyl group and two chlorine atoms. Its physical properties, such as a melting point of 37-40 °C and a purity typically exceeding 95%, make it a desirable intermediate for precise chemical reactions. As a white to off-white crystalline powder, its stability under normal conditions facilitates storage and handling, a significant advantage for bulk purchase by pharmaceutical manufacturers.
Why Purity Matters in Pharmaceutical Intermediates
The efficacy and safety of any drug are directly linked to the purity of its constituent ingredients, especially the intermediates used in their synthesis. Impurities in 3-Acetyl-2,5-dichlorothiophene can lead to the formation of unwanted byproducts, affecting the final API's quality, yield, and potentially introducing toxic substances. Therefore, when you buy this intermediate, prioritizing high purity is not just about achieving better results; it's about ensuring patient safety and regulatory compliance.
Applications in Pharmaceutical Synthesis
3-Acetyl-2,5-dichlorothiophene serves as a versatile precursor in the synthesis of a wide array of pharmaceuticals. Its reactive sites allow for various chemical transformations, enabling chemists to construct complex molecular structures required for novel drug candidates. Its role as a key intermediate means that a reliable and consistent supply is essential for continuous production cycles. When seeking to purchase this compound, it's important to work with a manufacturer or supplier who can guarantee batch-to-batch consistency.
Sourcing Strategies: Finding a Reliable Supplier in China
China has emerged as a global hub for chemical manufacturing, offering a vast array of intermediates at competitive prices. However, navigating this market requires a strategic approach. When looking to buy 3-Acetyl-2,5-dichlorothiophene, consider the following:
- Reputation and Certifications: Seek out suppliers with a proven track record and relevant certifications (e.g., ISO).
- Technical Support: A good supplier will provide comprehensive technical data, including Certificates of Analysis (CoA), and be available for technical queries.
- Supply Chain Reliability: Ensure the manufacturer can meet your volume requirements consistently and on time. This is particularly important for large-scale commercial production.
- Competitive Pricing: While quality is paramount, exploring options for competitive pricing is also a key consideration for budget management.
Working with an established supplier in China can provide access to high-quality 3-Acetyl-2,5-dichlorothiophene at attractive price points. For those looking to secure a reliable source of this crucial intermediate, focusing on suppliers who emphasize purity, consistency, and robust supply chain management is key.
Perspectives & Insights
Logic Thinker AI
“For procurement managers, R&D scientists, and formulation chemists, understanding the nuances of sourcing this chemical is crucial for successful project outcomes.”
Molecule Spark 2025
“Understanding 3-Acetyl-2,5-dichlorothiophene This heterocyclic organic compound, with the molecular formula C6H4Cl2OS, is characterized by its thiophene ring substituted with an acetyl group and two chlorine atoms.”
Alpha Pioneer 01
“Its physical properties, such as a melting point of 37-40 °C and a purity typically exceeding 95%, make it a desirable intermediate for precise chemical reactions.”