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1072-11-3

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  • 2-[2-(dimethylazaniumyl)ethyldisulfanyl]ethyl-dimethylazanium dichloride

    Cas No: 1072-11-3

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1072-11-3 Usage

General Description

Bis[2-(dimethylamino)ethyl] persulfide is a chemical compound with the formula (C4H10NS2)2. It is an organic compound that contains two dimethylaminoethyl groups and two persulfide (-S-S-) groups. Bis[2-(dimethylamino)ethyl] persulfide is commonly used as a reagent in organic synthesis, particularly in the preparation of sulfur-containing compounds. It is also used as a curing agent for epoxy resins and as a vulcanizing agent for rubber. Bis[2-(dimethylamino)ethyl] persulfide is a highly reactive and versatile compound with a wide range of applications in various industries. Additionally, it is known to have strong odor and may cause irritation to eyes and skin upon exposure.

Check Digit Verification of cas no

The CAS Registry Mumber 1072-11-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,7 and 2 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1072-11:
(6*1)+(5*0)+(4*7)+(3*2)+(2*1)+(1*1)=43
43 % 10 = 3
So 1072-11-3 is a valid CAS Registry Number.

1072-11-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[2-(dimethylamino)ethyldisulfanyl]-N,N-dimethylethanamine

1.2 Other means of identification

Product number -
Other names 2,9-dimethyl-2,9-diaza-5,6-dithiadecane

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:1072-11-3 SDS

1072-11-3Upstream product

1072-11-3Relevant articles and documents

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

Keire, David A.,Strauss, Erin,Guo, Wei,Noszal, Bela,Rabenstein, Dallas L.

, p. 123 - 127 (2007/10/02)

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.

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