98264-26-7 Usage
Description
Tetrakis(1-Methylethyl)-2,10-diMethyl-3,3,9,9-4,8-dioxa-3,9-disilaundecan-6-ol, also known as protected glycerol (G598400), is a unique compound that plays a significant role in various laboratory applications. It is characterized by its ability to enhance the process of sample preparation and gel formation for polyacrylamide gel electrophoresis, a widely used technique in molecular biology and biochemistry.
Uses
Used in Molecular Biology and Biochemistry:
Tetrakis(1-Methylethyl)-2,10-diMethyl-3,3,9,9-4,8-dioxa-3,9-disilaundecan-6-ol is used as a protective agent in sample preparation for polyacrylamide gel electrophoresis. It helps to prevent the degradation of nucleic acids and proteins during the process, ensuring accurate and reliable results.
Used in Gel Formation for Polyacrylamide Gel Electrophoresis:
In the field of polyacrylamide gel electrophoresis, Tetrakis(1-Methylethyl)-2,10-diMethyl-3,3,9,9-4,8-dioxa-3,9-disilaundecan-6-ol serves as a crucial component in the formation of the gel matrix. Its presence contributes to the stability and uniformity of the gel, which is essential for the separation and analysis of biomolecules.
Used in Sample Preparation Industry:
Tetrakis(1-Methylethyl)-2,10-diMethyl-3,3,9,9-4,8-dioxa-3,9-disilaundecan-6-ol is used as a protective agent in the sample preparation industry, particularly for polyacrylamide gel electrophoresis. It helps to maintain the integrity of the samples, allowing for more accurate and consistent results in various applications, such as DNA sequencing, protein analysis, and forensic investigations.
Check Digit Verification of cas no
The CAS Registry Mumber 98264-26-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,8,2,6 and 4 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 98264-26:
(7*9)+(6*8)+(5*2)+(4*6)+(3*4)+(2*2)+(1*6)=167
167 % 10 = 7
So 98264-26-7 is a valid CAS Registry Number.
98264-26-7Relevant articles and documents
Total synthesis of 2-arachidonylglycerol (2-Ara-Gl)
Han, Luning,Razdan, Raj K.
, p. 1631 - 1634 (2007/10/03)
Total synthesis of 2-Arachidonylglycerol (2-Ara-Gl) was accomplished starting from arachidonic acid and glycerol. The sequence involves selective protection of the primary alcohols of glycerol, esterification, and mild hydrolysis of the protecting groups. A unique hydrolysis condition was developed to prevent isomerization of the 2-Ara-Gl to the more stable 1- monoglyceride.
