Di-tert-butyl 1,4,7,10-tetraazacyclododecane-1,7-dicarboxylate

95%

Reagent Code: #130135
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CAS Number 913542-69-5

science Other reagents with same CAS 913542-69-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 372.5 g/mol
Formula C₁₈H₃₆N₄O₄
badge Registry Numbers
MDL Number MFCD30532153
thermostat Physical Properties
Boiling Point 474.5±30.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.030±0.06 g/cm3(Predicted)
Storage 2-8°C, away from light, dry

description Product Description

Used as a key intermediate in the synthesis of macrocyclic ligands, particularly in the preparation of functionalized tetraazacyclododecane (DO3A) derivatives. These derivatives are widely employed in the development of MRI contrast agents due to their ability to form stable complexes with lanthanide ions such as gadolinium(III). The tert-butyl protecting groups allow selective modification of the nitrogen atoms, enabling controlled conjugation to targeting molecules or biomolecules in diagnostic imaging applications. Also utilized in radiopharmaceuticals and chelation therapy research owing to its favorable coordination properties and stability under physiological conditions.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,630.00
inventory 250mg
10-20 days ฿4,460.00
inventory 1g
10-20 days ฿11,980.00

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Di-tert-butyl 1,4,7,10-tetraazacyclododecane-1,7-dicarboxylate
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Used as a key intermediate in the synthesis of macrocyclic ligands, particularly in the preparation of functionalized tetraazacyclododecane (DO3A) derivatives. These derivatives are widely employed in the development of MRI contrast agents due to their ability to form stable complexes with lanthanide ions such as gadolinium(III). The tert-butyl protecting groups allow selective modification of the nitrogen atoms, enabling controlled conjugation to targeting molecules or biomolecules in diagnostic imaging

Used as a key intermediate in the synthesis of macrocyclic ligands, particularly in the preparation of functionalized tetraazacyclododecane (DO3A) derivatives. These derivatives are widely employed in the development of MRI contrast agents due to their ability to form stable complexes with lanthanide ions such as gadolinium(III). The tert-butyl protecting groups allow selective modification of the nitrogen atoms, enabling controlled conjugation to targeting molecules or biomolecules in diagnostic imaging applications. Also utilized in radiopharmaceuticals and chelation therapy research owing to its favorable coordination properties and stability under physiological conditions.

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