DOTA Tris-(t-butyl ester) Ethylenediamino Monoamide
98%
- Product Code: 87747
CAS:
173308-19-5
Molecular Weight: | 614.82 g./mol | Molecular Formula: | C₃₀H₆₈N₆O₇ |
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Density: | Storage Condition: | room temperature |
Product Description:
DOTA Tris-(t-butyl ester) Ethylenediamino Monoamide is widely used in the field of radiopharmaceuticals, particularly in the development of imaging agents for positron emission tomography (PET) and magnetic resonance imaging (MRI). Its chelating properties make it highly effective for binding with metal ions, such as gadolinium or radioactive isotopes like gallium-68, which are essential for diagnostic imaging. This compound is often employed in the synthesis of targeted contrast agents, enabling precise visualization of tumors, inflammation, or other abnormalities in the body. Its stability and ability to form strong complexes with metals also make it valuable in therapeutic applications, such as in radioimmunotherapy, where it helps deliver radioactive isotopes directly to cancer cells. Additionally, its t-butyl ester groups provide protection during synthesis, allowing for controlled and efficient modification of the molecule for specific applications.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.010 | 10-20 days | $520.28 |
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DOTA Tris-(t-butyl ester) Ethylenediamino Monoamide
DOTA Tris-(t-butyl ester) Ethylenediamino Monoamide is widely used in the field of radiopharmaceuticals, particularly in the development of imaging agents for positron emission tomography (PET) and magnetic resonance imaging (MRI). Its chelating properties make it highly effective for binding with metal ions, such as gadolinium or radioactive isotopes like gallium-68, which are essential for diagnostic imaging. This compound is often employed in the synthesis of targeted contrast agents, enabling precise visualization of tumors, inflammation, or other abnormalities in the body. Its stability and ability to form strong complexes with metals also make it valuable in therapeutic applications, such as in radioimmunotherapy, where it helps deliver radioactive isotopes directly to cancer cells. Additionally, its t-butyl ester groups provide protection during synthesis, allowing for controlled and efficient modification of the molecule for specific applications.
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