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5325-76-8

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5325-76-8 Usage

Description

4,4'-DITHIOBISPHENYLACETIC ACID, also known as DTBP, is an organic compound that serves as a redox buffer. It is characterized by its ability to increase the folding rate of disulfide-containing proteins compared to traditional buffers like glutathione and glutathione-disulfide. This property makes it a valuable tool in various applications across different industries.

Uses

Used in Biochemistry and Molecular Biology:
4,4'-DITHIOBISPHENYLACETIC ACID is used as a redox buffer for increasing the folding rate of disulfide-containing proteins. Its application reason is to enhance protein folding efficiency and improve the overall yield of correctly folded proteins, which is crucial for various research and diagnostic applications.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 4,4'-DITHIOBISPHENYLACETIC ACID is used as a stabilizing agent for protein-based drugs. The application reason is to improve the stability and shelf life of these drugs by maintaining the correct disulfide bond formation and preventing protein aggregation.
Used in Diagnostics:
4,4'-DITHIOBISPHENYLACETIC ACID is used as a component in diagnostic assays that require the detection or quantification of disulfide-containing proteins. The application reason is to ensure accurate and reliable results by providing an optimal redox environment for protein folding and stability.
Used in Research and Development:
In research and development, 4,4'-DITHIOBISPHENYLACETIC ACID is used as a tool for studying protein folding and disulfide bond formation. The application reason is to gain a better understanding of the underlying mechanisms and to develop new strategies for protein engineering and drug design.
Overall, 4,4'-DITHIOBISPHENYLACETIC ACID is a versatile compound with a wide range of applications in various industries, primarily due to its ability to act as a redox buffer and improve the folding rate of disulfide-containing proteins.

Check Digit Verification of cas no

The CAS Registry Mumber 5325-76-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,3,2 and 5 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 5325-76:
(6*5)+(5*3)+(4*2)+(3*5)+(2*7)+(1*6)=88
88 % 10 = 8
So 5325-76-8 is a valid CAS Registry Number.

5325-76-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[4-[[4-(carboxymethyl)phenyl]disulfanyl]phenyl]acetic acid

1.2 Other means of identification

Product number -
Other names 4,4'-dithiobisbenzeneacetic acid

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:5325-76-8 SDS

5325-76-8Downstream Products

5325-76-8Relevant articles and documents

Folding disulfide-containing proteins faster with an aromatic thiol

Gough, Jonathan D.,Williams Jr., Rhondye H.,Donofrio, Anthony E.,Lees, Watson J.

, p. 3885 - 3892 (2002)

The traditional method for in vitro folding of disulfide-containing proteins is slow and involves a redox buffer of glutathione and glutathione disulfide. To increase the folding rate and to gain insight into the folding process, we replaced glutathione, an aliphatic thiol, with a commercially available aromatic thiol, 4-mercaptobenzeneacetate (1). Aromatic thiol 1 was selected due to its enhanced nucleophilicity and its enhanced leaving-group ability relative to glutathione at pH 7.7. To demonstrate the advantages of 1, the folding of reduced and scrambled RNase A at pH 7.0 and 7.7 in the presence of 1 and glutathione was investigated. For each set of folding conditions, the optimum concentration of each thiol was initially determined and then the folding rates in the presence of each thiol were measured concurrently. In all cases examined, the folding rate enhancement with the aromatic thiol was 5- 6-fold. Furthermore, under similar conditions folding rates were almost identical with either reduced or scrambled RNase A. In addition the 5-6-fold folding rate enhancement varied only slightly with pH, 7.0 vs 7.7.

METHOD FOR PATHOGENS, MICROORGANISMS, AND PARASITES INACTIVATION

-

Paragraph 0221-0224, (2020/02/16)

The invention provides a method for inactivation or reduction of pathogens, microorganisms or parasites in a sample, media, composition, utility, device, surface or organism by treatment with an alkylating compound of Structure I, followed by elimination or reduction of the residual compound with Structure I by treatment with a neutralizing agent, which eliminates or reduces the toxicity or other undesirable properties of the alkylating compound with Structure I. The neutralizing agent may be present in a treatment solution or be part of a solid-phase agent, and preferably acts by eliminating the alkylating properties of the compound of Structure I.

Enzymatic thiol Michael addition using laccases: Multiple C-S bond formation between p-hydroquinones and aromatic thiols

Schlippert, Max,Mikolasch, Annett,Hahn, Veronika,Schauer, Frieder

supporting information, p. 106 - 114 (2016/02/27)

Laccases create C-C, C-O or C-N bonds and have been investigated intensively as catalysts for green chemistry and white biotechnology. However, little is known about C-S bond formation in laccase-catalyzed reactions. We have used the laccases from Pycnopo

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