107-55-1

Usage

Uses

Used in Mining Industry:
O,O-di-sec-butyl hydrogen dithiophosphate is used as a flotation reagent for selectively binding to the surfaces of certain minerals, facilitating their separation from waste material during the flotation process.
Used in Pesticide Production:
In the agricultural sector, O,O-di-sec-butyl hydrogen dithiophosphate is utilized in the production of pesticides, playing a crucial role in enhancing the effectiveness of these products.
Used in Lubricating Oils:
O,O-di-sec-butyl hydrogen dithiophosphate serves as an antioxidant in lubricating oils, helping to prolong the life of the oil and improve the performance of machinery by reducing wear and tear.
It is important to handle and dispose of O,O-di-sec-butyl hydrogen dithiophosphate with care due to its potential hazards, ensuring safety in its applications across various industries.

InChI:InChI=1/C8H19O2PS2/c1-5-7(3)9-11(12,13)10-8(4)6-2/h7-8H,5-6H2,1-4H3,(H,12,13)

Upstream product

• 78-92-2 iso-butanol 

Downstream Products

• 513-53-1 1-methyl-1-propanethiol 

Relevant academic research and scientific papers

A 31P NMR Study of O,O'-Dialkyldithiophosphates: An Unusual Coupling

A series of O,O'-dialkyldithiophosphoric acids have been studied by 31P NMR, and a four-bond 31P-1H scalar coupling has been detected.This coupling is unusual because it is observed between phosphorus and only one of two available protons located on the same carbon, even when the alkyl fragment is simply an alkane that should not show conformational preference.Variation of the structural features of alkyl group showed that this coupling involved a "W" pathway. KEY WORDS - 31P NMR O,O'-dialkyldithiophosphoric acids four-bond 31P, 1H coupling

Pyridoxonium salts of chiral and cyclic dithiophosphoric and bisdithiophosphonic acids and their antimicrobial activities

Pyridoxonium salts of chiral linear and cyclic dithiophosphoric acids were obtained by the reactions of pyridoxine with bis{2-О-[2-methyl-(2S)-3-O-propionyl]}, bis{2-О-[1,4-О,О-dimethyl-(2S)-succinyl]}, and O,O-di-2-butyl dithiophosphoric acids, and cyclic dithiophosphoric acids of 1,3,2-dioxaphosphorinane, 1,3,2-dioxaphospholane, and 1,3,2-dioxaphosphepin structure. Syntheses of acetonide pyridoxonium О,О-dimenthyl dithiophosphates were carried out by the reaction of seven-membered pyridoxine acetonide with О,О-dimenthyl dithiophosphoric acids obtained from (–)-(1 R,2S,5R)-menthol and (+)-(1S,2R,5S)-menthol. Diacetonide pyridoxonium bisdithiophosphonate was also prepared. The antibacterial and antifungal activities of pyridoxonium chiral linear and cyclic dithiophosphates were evaluated.