1072-11-3

Usage

Uses

Used in Organic Synthesis:
Bis[2-(dimethylamino)ethyl] persulfide is utilized as a reagent in organic synthesis, particularly for the preparation of sulfur-containing compounds. Its unique structure and reactivity make it a valuable component in the creation of a variety of chemical products.
Used in Epoxy Resin Industry:
In the epoxy resin industry, Bis[2-(dimethylamino)ethyl] persulfide serves as a curing agent. It is used to harden and set the epoxy, providing a strong and durable final product that is resistant to various environmental factors.
Used in Rubber Industry:
Bis[2-(dimethylamino)ethyl] persulfide is also employed as a vulcanizing agent in the rubber industry. It helps to cross-link the polymer chains in rubber, enhancing the material's strength, elasticity, and resistance to wear.
Used in Chemical Research:
Due to its reactivity and unique chemical properties, Bis[2-(dimethylamino)ethyl] persulfide is also used in chemical research for studying reactions involving sulfur and for developing new synthetic pathways and methodologies.

Upstream product

• 108-02-1 captamine 

Downstream Products

• 10498-85-8 2,2'-disulfanediylbis(N,N,N-trimethylethan-1-ammonium) diiodide 
• 108-02-1 captamine 
• 1581704-44-0 (2S,3R)-N-((2-(Dimethylamino)ethyl)sulfanyl)-N’-((3S)-1-methyl-2-oxo-5-phenyl-2,3-dihydro-1H-1,4-benzodiazepin-3-yl)-2,3-bis(3,3,3-trifluoropropyl)succinamide 

Relevant academic research and scientific papers

Kinetics and Equilibria of Thiol/Disulfide Interchange Reactions of Selected Biological Thiols and Related Molecules with Oxidized Glutathione

Rate constants for reaction of coenzyme A and cysteine with oxidized glutathione (GSSG) and equilibrium constants for the reaction of coenzyme A, cysteine, homocysteine, cysteamine, and related thiols with GSSG by thiol/disulfide interchange were determined over a range of pD values by NMR spectroscopy.The rate constants for reaction of the thiolate anion forms of coenzyme A and cysteine with GSSG suggest that reduction of GSSG by coenzyme A and cysteine is a mechanistically uncomplicated SN2 reaction.Equilibrium constants for the thiol/disulfide interchange reactions show a strong dependence on the Bronsted basicity of the thiolate anion.In a similar way, ΔE0', the difference between the half-cell potentials for the RSSR/RSH and GSSG/GSH redox couples, is linearly dependent on the difference between the pKA values of RSH and glutathione: ΔE0' = 64ΔpKA - 7.7 where ΔE0' is in units of mV.The reducing strength at a given pH is also determined by the fraction of the thiol present in the reactive thiolate form.At pD 7, the half-cell potentials for coenzyme A, cysteine, homocysteine, and cysteamine are close to that of glutathione, the major intracellular thiol redox system, which suggests that small changes in the intracellular redox potential can cause significant changes in the intracellular distribution of these biological thiols between their reduced and oxidized forms.