4-Aminobutyl-DOTA-tris (t-butyl ester)

95%

  • Product Code: 83160
  CAS:    1402393-59-2
Molecular Weight: 642.87 g./mol Molecular Formula: C₃₂H₆₂N₆O₇
EC Number: MDL Number:
Melting Point: Boiling Point: 710.0±60.0 °C(Predicted)
Density: 1.050±0.06 g/cm3(Predicted) Storage Condition: 2-8°C, protected from light, inert gas
Product Description: 4-Aminobutyl-DOTA-tris (t-butyl ester) is primarily used in the field of radiopharmaceuticals and medical imaging. It serves as a key chelating agent for binding metal ions, particularly lanthanides and actinides, which are essential in the development of contrast agents for magnetic resonance imaging (MRI). Its ability to form stable complexes with gadolinium ions makes it valuable in enhancing the quality of MRI scans by improving contrast in tissues and organs. Additionally, it is utilized in the synthesis of targeted therapeutic agents, where it helps deliver radioactive isotopes to specific cells or tissues for diagnostic or therapeutic purposes, such as in cancer treatment. Its t-butyl ester groups provide protection during synthesis, ensuring the molecule remains intact until it reaches the desired site of action.
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.025 10-20 days Ft78,640.21
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0.100 10-20 days Ft153,983.55
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4-Aminobutyl-DOTA-tris (t-butyl ester)
4-Aminobutyl-DOTA-tris (t-butyl ester) is primarily used in the field of radiopharmaceuticals and medical imaging. It serves as a key chelating agent for binding metal ions, particularly lanthanides and actinides, which are essential in the development of contrast agents for magnetic resonance imaging (MRI). Its ability to form stable complexes with gadolinium ions makes it valuable in enhancing the quality of MRI scans by improving contrast in tissues and organs. Additionally, it is utilized in the synthesis of targeted therapeutic agents, where it helps deliver radioactive isotopes to specific cells or tissues for diagnostic or therapeutic purposes, such as in cancer treatment. Its t-butyl ester groups provide protection during synthesis, ensuring the molecule remains intact until it reaches the desired site of action.
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