Trithioacetone, with the CAS number 828-26-2, is a chemical compound characterized by its unique structure, which includes three sulfur atoms bonded to a central carbon framework. It is classified as a thioester and is known for its distinctive odor, often described as resembling that of rotten eggs due to the presence of sulfur. Trithioacetone is typically a colorless to pale yellow liquid at room temperature and is soluble in organic solvents. Its chemical formula is C6H10S3, indicating the presence of carbon, hydrogen, and sulfur in its molecular structure. This compound is of interest in various fields, including organic synthesis and materials science, due to its potential applications in the development of novel chemical processes and products. Additionally, trithioacetone can participate in various chemical reactions, including nucleophilic substitutions and redox reactions, making it a versatile compound in synthetic chemistry. Safety precautions should be observed when handling trithioacetone, as it may pose health risks if inhaled or ingested.

Trithioacetone

828-26-2: 1,3,5-Trithiane, 2,2,4,4,6,6-Hexamethyl-, 2,2,4,4,6,6-Hexamethyl-S-Trithiane, 212-582-5, Hexamethyl-1,3,5-trithiane, Hexamethyl-s-trithiane, Trithioacetone, s-Trithiane, 2,2,4,4,6,6-hexamethyl-, s-Trithiane, hexamethyl-, 2,2,4,4,6,6-Hexamethyl-1,3,5-trithiane,  2,2,4,4,6,6-Hexamethyl-1,3,5-trithiane

2,2,4,4,6,6-Hexamethyl-1,3,5-trithiane

2,2,4,4,6,6-Hexamethyl-S-trithiane

Hexamethyl-1,3,5-trithiane(2,2,4,4,6,6-Hexamethyl-S-trithiane) is used in flavor preparation, organic synthesis and biochemical experiments.

CAS 828-26-2: Trithioacetone

2,2,4,4,6,6-Hexamethyl-1,3,5-trithiane

Ref: IN-DA0055UU

2,2,4,4,6,6-Hexamethyl-1,3,5-trithiane

Ref: 3B-H1278

2,2,4,4,6,6-Hexamethyl-1,3,5-trithiane

Ref: 10-F239302

2,2,4,4,6,6-Hexamethyl-S-trithiane

Ref: 54-OR1009877

Hexamethyl-1,3,5-trithiane

Ref: TM-T203854