12034-39-8 | SODIUM TETRASULFIDE

Packsize	Purity	Availability	Price	Discounted Price
5g	30%	2 weeks	$58.00	$40.00
25g	30%	2 weeks	$110.00	$77.00
500g	30%	2 weeks	$861.00	$603.00

Description

• Catalog Number: AE16702
• Chemical Name: SODIUM TETRASULFIDE
• CAS Number: 12034-39-8
• Molecular Formula: Na2S4
• Molecular Weight: 174.23953999999998
• MDL Number: MFCD00014249
• SMILES: [Na]SSSS[Na]

Upstream Synthesis Route

Sodium tetrasulfide is a versatile chemical compound that finds its application in various areas of chemical synthesis. One of the key uses of sodium tetrasulfide in chemical synthesis is as a reagent for the preparation of organosulfur compounds. By reacting sodium tetrasulfide with organic halides or epoxides, organosulfur compounds such as thioethers and thiols can be efficiently synthesized. This reaction pathway offers a reliable and cost-effective method for the incorporation of sulfur functionalities into organic molecules.Furthermore, sodium tetrasulfide can also act as a sulfur transfer reagent in chemical transformations. In reactions involving the transfer of sulfur atoms, sodium tetrasulfide serves as a convenient source of sulfur, enabling the construction of sulfur-containing compounds with high selectivity and efficiency. Additionally, its role as a sulfur transfer agent facilitates the functionalization of organic molecules with sulfur moieties, expanding the synthetic possibilities in medicinal chemistry, materials science, and other fields.Moreover, sodium tetrasulfide can be employed as a reducing agent in certain chemical reactions. Its ability to donate electrons enables the reduction of various functional groups, leading to the formation of new chemical bonds and the synthesis of diverse molecular structures. By harnessing the reducing power of sodium tetrasulfide, chemists can access novel compounds and intricate chemical architectures that would otherwise be challenging to obtain.In summary, sodium tetrasulfide serves as a valuable tool in chemical synthesis, offering diverse pathways for the construction of sulfur-containing compounds, sulfur transfer reactions, and redox transformations. Its versatility and utility make it a go-to reagent for synthetic chemists seeking to access a wide range of sulfur-based molecules with tailored properties and functionalities.