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Glutathionesulfonic acid, a derivative of the naturally occurring antioxidant glutathione, is a water-soluble molecule that plays a vital role in detoxifying the body by neutralizing harmful substances such as free radicals and reactive oxygen species. It is involved in the regulation of cellular redox balance and the maintenance of proper function of enzymes and proteins. Glutathionesulfonic acid has been studied for its potential therapeutic applications, including its ability to protect cells from oxidative stress and its role in the treatment of various medical conditions such as liver disease and certain types of cancer.

3773-07-7

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3773-07-7 Usage

Uses

Used in Pharmaceutical Industry:
Glutathionesulfonic acid is used as a therapeutic agent for its potential role in protecting cells from oxidative stress and its involvement in the treatment of various medical conditions such as liver disease and certain types of cancer.
Used in Cosmetic and Skincare Industry:
Glutathionesulfonic acid is used as a skin-lightening and anti-aging ingredient in cosmetic and skincare products due to its purported benefits for the skin.

Check Digit Verification of cas no

The CAS Registry Mumber 3773-07-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,7,7 and 3 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 3773-07:
(6*3)+(5*7)+(4*7)+(3*3)+(2*0)+(1*7)=97
97 % 10 = 7
So 3773-07-7 is a valid CAS Registry Number.

3773-07-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name Glutathionesulfonic acid

1.2 Other means of identification

Product number -
Other names Glutathione sulfonate

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:3773-07-7 SDS

3773-07-7Downstream Products

3773-07-7Relevant academic research and scientific papers

Direct electrochemical oxidation of disulfides at anodically pretreated boron-doped diamond electrodes

Terashima,Rao, Tata N.,Sarada,Kubota,Fujishima

, p. 1564 - 1572 (2003)

Anodically oxidized diamond electrodes have been used to oxidize disulfides, thiols, and methionine in aqueous acidic media and tested for amperometric detection of these compounds after chromatographic separation. Cyclic voltammetric signals for 1 mM glutathione disulfide (GSSG) were observed at 1.39 and 1.84 V vs SCE, the values being less positive than those of its as-deposited counterpart as well as glassy carbon electrode. The voltammetric and chronocoulometric results have indicated the high stability of the electrode with negligible adsorption. A positive shift in the peak potential with increasing pH indicated the attractive electrostatic interaction between the anodically oxidized diamond surface and the positively charged GSSG in acidic media that promoted its analytical performance. The results of the electrolysis experiments of disulfides and thiols showed that the oxidation reaction mechanism of glutathione (GSH) and GSSG involves oxygen transfer. Following separation by liquid chromatography (LC), the determination of both GSH and GSSG in rat whole blood was achieved at a constant potential (1.50 V vs Ag/AgCl), and the limits of detection for GSH and GSSG were found to be 1.4 nM (0.028 pmol) and 1.9 nM (0.037 pmol) with a linear calibration range up to 0.25 mM. These detection limits were much lower than those reported for the amperometry using Bi-PbO2 electrodes and LC-mass spectrometry, and the LC method using diamond electrodes were comparable with enzymatic assay in real sample analysis. The high response stability and reproducibility together with the possibility of regeneration of the electrode surface by on-line anodic treatment at 3 V for 30 min further support the applicability of anodically pretreated diamond for amperometric detection of disulfides.

Kinetics and mechanism of the reactions of superoxochromium(III) ion with biological thiols

Perez-Benito, Joaquin F.,Arias, Conchita

, p. 5837 - 5845 (2007/10/03)

The kinetics of the oxidation of three biological thiols (L-cysteine, glutathione, and DL-penicillamine) to their sulfinic and sulfonic acid derivatives by CrOO2+ in aqueous perchloric acid and in the presence of 2-propanol have been studied spectrophotometrically with the aid of the initial-rates method. The kinetic order of the oxidant is 2, whereas that of the reductant is not defined. The acidity of the medium has a slight effect on the initial rates (acid catalysis for both L-cysteine and DL-penicillamine and base catalysis for glutathione). An increase of the ionic strength leads to a rise of the initial rate for both L-cysteine and DL-penicillamine, whereas the initial rate for glutathione is insensitive to the ionic strength. The reactions are inhibited by both 2-propanol and dissolved O2 and catalyzed by Mn2+, whereas Ce3+ has almost no effect on them. At low 2-propanol concentration and in the absence of Mn2+ the initial rate vs temperature plots have a minimum at around 20 °C, whereas in the presence of either concentrated 2-propanol or Mn2+ the Arrhenius law is fulfilled. A single mechanism is proposed for the three reactions involving a CrOO2+/thiol complex, CrOOH2+, and CrO2+ as intermediates. The bimolecular rate constants for the reactions of the intermediate CrO2+ with L-cysteine and DL-penicillamine at 25.0 °C have been obtained (around 103 M-1 s-1 in both cases). Some kinetic data for the decomposition of CrOO2+ in the absence of thiol are also given.

Oxidative Cleavage of Peptide and Protein Disulphide Bonds by Gold(III): a Mechanism for Gold Toxicity

Witkiewicz, Patricia L.,Shaw, C. Frank

, p. 1111 - 1114 (2007/10/02)

The oxidative cleavage of disulphide bonds to form the sulphonic acid derivatives is shown to be an important reaction of AuX4- (X = Cl, Br) with proteins and peptides; the implications of this reaction for the toxicity of gold compounds are discussed.

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