496839-01-1

Basic information

• Product Name: 20-(11-Mercaptoundecanyloxy)-3,6,9,12,15,18-hexaoxaeicosane-1-amine,hydrochloride
• Synonyms: 20-(11-Mercaptoundecanyloxy)-3,6,9,12,15,18-hexaoxaeicosane-1-amine,hydrochloride
• CAS NO: 496839-01-1
• Molecular Formula: C₂₃H₄₉NO₆S
• Molecular Weight: 467.7
• Mol File: 496839-01-1.mol

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 20-(11-Mercaptoundecanyloxy)-3,6,9,12,15,18-hexaoxaeicosane-1-amine,hydrochloride(CAS DataBase Reference)
• NIST Chemistry Reference: 20-(11-Mercaptoundecanyloxy)-3,6,9,12,15,18-hexaoxaeicosane-1-amine,hydrochloride(496839-01-1)
• EPA Substance Registry System: 20-(11-Mercaptoundecanyloxy)-3,6,9,12,15,18-hexaoxaeicosane-1-amine,hydrochloride(496839-01-1)

Safety Data

• Hazardous Substances Data: 496839-01-1(Hazardous Substances Data)

Usage

Chemical compound

20-(11-Mercaptoundecanyloxy)-3,6,9,12,15,18-hexaoxaeicosane-1-amine, hydrochloride

Structure

contains a 20-carbon hydrocarbon chain with six ethylene glycol units, a thiol group, and an amine group attached to the 20th carbon

Properties

long hydrocarbon chain, amine group, thiol group, hydrochloride salt
Formed when the amine group reacts with hydrochloric acid
Potential applications in pharmaceuticals, materials science, and other fields due to its unique structure and properties.

Upstream product

• 578730-38-8 S-(1-azido-3,6,9,12,15,18-hexaoxanonacosan-29-yl) ethanethioate 
• 1043884-40-7 O-tosyl-(ω-undec-10-enyl) hexaethylene glycol 
• 1310815-11-2 C₃₃H₆₃NO₁₀ 
• 2615-15-8 pentaethylene glycol 
• 7766-50-9 1-undecen-11-ylbromide 
• 130727-48-9 3,6,9,12,15,18-hexaoxa-28-nonacosen-1-ol 

Downstream Products

• 496837-01-5 C₄₂H₆₃NO₆S 

Relevant articles and documents

Facile method for development of ligand-patterned substrates induced by a chemical reaction

Choose a pattern: A simple and efficient method for ligand patterning on a surface is reported. An organic chemical reaction induces various patterns of an amine functional group, which is further conjugated to a cell adhesion ligand to result in cell patterning (see figure). Copyright

Synthesis of benzaldehyde-functionalized glycans: A novel approach towards glyco-SAMs as a tool for surface plasmon resonance studies

In recent years the interest in tools for investigating carbohydrateprotein (CPI) and carbohydrate-carbohydrate interactions (CCI) has increased significantly. For the investigation of CPI and CCI, several techniques employing different linking methods are available. Surface plasmon resonance (SPR) imaging is a most appropriate tool for analyzing the formation of self-assembled monolayers (SAM) of carbohydrate derivatives, which can mimic the glycocalyx. In contrast to the SPR imaging methods used previously to analyze CPI and CCI, the novel approach reported herein allows a facile and rapid synthesis of linker spacers and carbohydrate derivatives and enhances the binding event by controlling the amount and orientation of ligand. For immobilization on biorepulsive amino-functionalized SPR chips by reductive amination, diverse aldehyde-functionalized glycan structures (glucose, galactose, mannose, glucosamine, cellobiose, lactose, and lactosamine) have been synthesized in several facile steps that include olefin metathesis. Effective immobilization and the first binding studies are presented for the lectin concanavalin A.