253678-67-0 Usage
Description
UNDECYL MALTOSIDE-SOL-GRADE is a non-ionic, non-foaming, and water-soluble detergent that is specifically designed for the purification, extraction, and solubilization of membrane-bound proteins in their native structure. It enhances solubilization by dissociating aggregates and can be easily removed by dialysis, making it a valuable tool in various applications across different industries.
Uses
Used in Biochemistry and Molecular Biology Research:
UNDECYL MALTOSIDE-SOL-GRADE is used as a detergent for the purification, extraction, and solubilization of membrane-bound proteins in their native structure. It is particularly useful in research applications where maintaining the native structure of proteins is crucial for understanding their function and interactions.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, UNDECYL MALTOSIDE-SOL-GRADE is used as a solubilizing agent for membrane-bound proteins, which can be important for drug discovery and development. Its ability to dissociate aggregates and maintain protein structure makes it a valuable tool for studying protein targets and developing new therapeutic agents.
Used in Diagnostics and Clinical Research:
UNDECYL MALTOSIDE-SOL-GRADE is used as a detergent in the development of diagnostic assays and clinical research applications. Its ability to solubilize membrane-bound proteins can help in the detection and analysis of biomarkers, as well as in the development of new diagnostic tools.
Used in Protein Crystallography:
In protein crystallography, UNDECYL MALTOSIDE-SOL-GRADE is used as a detergent to solubilize membrane-bound proteins, facilitating the formation of protein crystals. This is essential for determining the three-dimensional structure of proteins, which can provide valuable insights into their function and potential drug targets.
Used in Nanotechnology and Materials Science:
UNDECYL MALTOSIDE-SOL-GRADE is used as a stabilizing agent in the development of nanomaterials and advanced materials. Its ability to solubilize and stabilize membrane-bound proteins can be useful in creating new materials with unique properties and applications.
Check Digit Verification of cas no
The CAS Registry Mumber 253678-67-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,5,3,6,7 and 8 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 253678-67:
(8*2)+(7*5)+(6*3)+(5*6)+(4*7)+(3*8)+(2*6)+(1*7)=170
170 % 10 = 0
So 253678-67-0 is a valid CAS Registry Number.
253678-67-0Relevant articles and documents
Highly β-Selective Glycosylation Reactions for the Synthesis of ω-Functionalized Alkyl β-Maltoside as a Co-crystallizing Detergent
Elias, M.,Hossain, M. A.,Jamil, M. A. R.,Rahman, M. M.,Siddiki, S. M. A. Hakim
, p. 1806 - 1814 (2020/12/01)
Abstract: Methods have been reported for the preparation of ω-functionalized alkyl maltoside and glycoside detergents via a simple and inexpensive synthetic route. The key step was stannic chloride-mediated glycosylation of long-chain alcohols or thiols with maltose octaacetate at 0 or –10°C, respectively, within a very short time (isolated yield 17–44%), which provided more than 98% β-selectivity.
Synthesis of C7-C16-Alkyl maltosides in the presence of tin(IV) chloride as a lewis acid catalyst
Markovic, Zoran,Predojevic, Jasmina,Manojlovic, Nedeljko T.
experimental part, p. 83 - 90 (2012/05/20)
The synthesis of C7- to C16-alkyl maltosides in the presence of tin(IV) chloride as Lewis acid catalyst was performed. The characterization of the products and theoretical investigation of the crucial step in the synthesis were carried out. The preparation of the β-maltosides required reaction time of 1 h, and that of the α-maltosides was 72 h. The side products were the α-D-maltosidechloride and 2-hydroxy-β-maltoside, respectively. The PM3 calculation confirmed the formation of the kinetically controlled β-product.
