1,4,7,10-Tetrabenzyl-1,4,7,10-tetraazacyclododecane

≥97%

Reagent Code: #69122
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CAS Number 18084-64-5

science Other reagents with same CAS 18084-64-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 532.78 g/mol
Formula C₃₆H₄₄N₄
thermostat Physical Properties
Melting Point 143-147°C
inventory_2 Storage & Handling
Storage room temperature

description Product Description

This compound, a tetra-benzylated derivative of cyclen (1,4,7,10-tetraazacyclododecane), serves primarily as a protected intermediate in coordination chemistry for synthesizing advanced ligands. The benzyl groups protect the nitrogen atoms, facilitating selective functionalization to create macrocyclic chelators that form stable complexes with metal ions, including transition metals and lanthanides like gadolinium. It is valuable in catalysis, material synthesis (e.g., metal-organic frameworks or MOFs), and the development of MRI contrast agents, where deprotected or modified derivatives effectively chelate gadolinium for medical imaging. Additionally, it supports research on metal ion behavior in biological systems and the creation of niche materials with specific properties.

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Test Parameter Specification
Appearance White to almost white powder to crystal
Purity 96.5-100
Infrared Spectrum Conforms to Structure

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿8,890.00
inventory 200mg
10-20 days ฿2,960.00

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1,4,7,10-Tetrabenzyl-1,4,7,10-tetraazacyclododecane
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This compound, a tetra-benzylated derivative of cyclen (1,4,7,10-tetraazacyclododecane), serves primarily as a protected intermediate in coordination chemistry for synthesizing advanced ligands. The benzyl groups protect the nitrogen atoms, facilitating selective functionalization to create macrocyclic chelators that form stable complexes with metal ions, including transition metals and lanthanides like gadolinium. It is valuable in catalysis, material synthesis (e.g., metal-organic frameworks or MOFs),

This compound, a tetra-benzylated derivative of cyclen (1,4,7,10-tetraazacyclododecane), serves primarily as a protected intermediate in coordination chemistry for synthesizing advanced ligands. The benzyl groups protect the nitrogen atoms, facilitating selective functionalization to create macrocyclic chelators that form stable complexes with metal ions, including transition metals and lanthanides like gadolinium. It is valuable in catalysis, material synthesis (e.g., metal-organic frameworks or MOFs), and the development of MRI contrast agents, where deprotected or modified derivatives effectively chelate gadolinium for medical imaging. Additionally, it supports research on metal ion behavior in biological systems and the creation of niche materials with specific properties.

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