113842-78-7

Basic information

• Product Name: 6-trityl-2,3,4,2’,3’,4’6’-hepta-O-acetyl-α,α’-D-trehalose
• Synonyms: 6-trityl-2,3,4,2’,3’,4’6’-hepta-O-acetyl-α,α’-D-trehalose
• CAS NO: 113842-78-7
• Molecular Weight: 878.881
• Mol File: 113842-78-7.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 6-trityl-2,3,4,2’,3’,4’6’-hepta-O-acetyl-α,α’-D-trehalose(CAS DataBase Reference)
• NIST Chemistry Reference: 6-trityl-2,3,4,2’,3’,4’6’-hepta-O-acetyl-α,α’-D-trehalose(113842-78-7)
• EPA Substance Registry System: 6-trityl-2,3,4,2’,3’,4’6’-hepta-O-acetyl-α,α’-D-trehalose(113842-78-7)

Safety Data

• Hazardous Substances Data: 113842-78-7(Hazardous Substances Data)

Upstream product

• 99-20-7 TREHALOSE 
• 108-24-7 acetic anhydride 
• 76-83-5 trityl chloride 
• 76054-83-6 6-O-trityl-α,α-trehalose 

Downstream Products

• 35014-66-5 6-O-Tosyl-hepta-O-acetyl-α,α-trehalose 
• 76054-83-6 6-O-trityl-α,α-trehalose 

Relevant articles and documents

Inhibition of S. aureus Infection of Human Umbilical Vein Endothelial Cells (HUVECs) by Trehalose- and Glucose-Functionalized Gold Nanoparticles

Microbial adhesion to host cells represents the initial step in the infection process. Several methods have been explored to inhibit microbial adhesion including the use of glycopolymers based on mannose, galactose, sialic acid and glucose. These sugar re

STABILIZATION OF BIOMOLECULES USING SUGAR POLYMERS

Compositions and methods for stabilizing biomolecules are disclosed. Specifically, the compositions include novel homopolymers or copolymers containing trehalose side chains conjugated to biomolecules. When such homopolymers or copolymers are placed in cl