The world of chemistry is built upon understanding the properties and reactivities of molecules. 2-Mercapto-4-methylpyrimidine Hydrochloride (CAS 6959-66-6) is a compound that, while perhaps not a household name, plays a significant role as a chemical intermediate in various synthesis processes. Its unique structure, featuring a pyrimidine ring with a mercapto group and a methyl substituent, endows it with valuable chemical characteristics. As a leading manufacturer, we are pleased to share insights into the chemistry of this compound and its importance.

Understanding the Molecular Structure and Properties

2-Mercapto-4-methylpyrimidine Hydrochloride belongs to the class of heterocyclic organic compounds. The pyrimidine core is a six-membered ring containing two nitrogen atoms, which is fundamental in many biological molecules, including DNA and RNA bases. The addition of a mercapto group (-SH) at the 2-position and a methyl group (-CH3) at the 4-position significantly alters its reactivity. The mercapto group, in particular, is a nucleophilic center and can readily undergo reactions such as alkylation and oxidation. The hydrochloride salt form (·HCl) typically enhances its solubility and stability, making it easier to handle in various reaction conditions.

The chemical formula C5H6N2S·HCl and a molecular weight of 162.64 g/mol are key identifiers. Its typical appearance as a yellow powder further aids in its identification. The melting point, often cited as decomposing around 265°C, indicates its stability under moderate temperatures but also suggests careful handling during reactions requiring higher heat.

Synthetic Utility and Applications

The real value of 2-Mercapto-4-methylpyrimidine Hydrochloride lies in its versatility as a synthetic intermediate. Chemists often buy this compound to:

  • Synthesize Thioethers: The mercapto group readily reacts with alkyl halides to form thioethers, which are important functional groups in pharmaceuticals and materials science.
  • Create Disulfides: Mild oxidation can lead to the formation of disulfide bonds, crucial in protein chemistry and some drug formulations.
  • Act as a Precursor for Pyrimidine Derivatives: The compound can be further functionalized at various positions on the ring, leading to a diverse array of pyrimidine-based compounds with potential biological activities or specific material properties.

These synthetic pathways are fundamental in the development of new drugs, agricultural chemicals, and advanced materials. For researchers and manufacturing firms, securing a high-purity source of 2-Mercapto-4-methylpyrimidine Hydrochloride (CAS 6959-66-6) is essential for predictable and successful synthesis outcomes.

Partnering with a Reliable Supplier

As a dedicated manufacturer, we understand the critical need for quality and consistency. We offer 2-Mercapto-4-methylpyrimidine Hydrochloride at 99% purity, backed by rigorous quality control. If you are looking to buy this essential intermediate, we encourage you to request a quote and experience the difference that a reliable supplier can make. Your success in chemical synthesis is our priority.