DOTA-Tris(tBu) Ester: Your Source for Advanced Bioconjugation
The intricate field of bioconjugation, which involves linking biomolecules with other molecular entities, is crucial for developing targeted therapeutics, advanced diagnostics, and innovative research tools. A key player in this domain is 2-[4,7,10-tris[2-[(2-methylpropan-2-yl)oxy]-2-oxoethyl]-1,4,7,10-tetrazacyclododec-1-yl]acetic acid, more commonly known as DOTA-Tris(tBu) ester (CAS: 137076-54-1). For those in the pharmaceutical and biotech industries, understanding its utility and where to buy DOTA-Tris(tBu) ester is essential.
DOTA-Tris(tBu) ester’s significance lies in its bifunctional nature. The DOTA macrocycle is a powerful chelator, capable of forming highly stable complexes with various metal ions. Critically, it features three tert-butyl ester protected carboxylate groups and one free carboxylic acid group. This unique structural design allows for controlled reactions. The free carboxylate is readily available for covalent attachment to biomolecules, such as peptides, antibodies, or nanoparticles, via standard peptide coupling chemistries. This makes it an ideal reagent for creating sophisticated molecular constructs.
When researchers look to purchase DOTA-Tris(tBu) ester, they are often seeking to leverage its ability to bridge the gap between targeting moieties and radioisotopes or imaging agents. The unprotected carboxylate can be activated using reagents like N-hydroxysuccinimide (NHS) or through direct coupling agents like HATU or HBTU, facilitating amide bond formation with amine-functionalized biomolecules. This controlled reactivity ensures that the conjugation occurs precisely at the desired site, maintaining the integrity of both the biomolecule and the chelator.
The applications of DOTA-Tris(tBu) ester in bioconjugation are vast and impactful. In the realm of radiopharmaceuticals, it is used to attach diagnostic or therapeutic radioisotopes to targeting vectors, enabling precise delivery to specific cells or tissues. For instance, conjugating DOTA-Tris(tBu) ester to a tumor-targeting peptide allows for the delivery of a radiometal payload that can be visualized via PET or SPECT imaging, or can deliver a therapeutic dose directly to the cancer cells. This precise targeting is a hallmark of advanced medical treatments.
Moreover, the synthesis of DOTA-Tris(tBu) ester itself is a testament to the careful design required in advanced chemical intermediates. The tert-butyl ester groups serve a dual purpose: they protect the carboxylates during synthesis and purification, and their selective removal under mild acidic conditions allows for the subsequent chelation of metal ions. This controlled deprotection and metalation strategy is crucial for producing high-quality radioconjugates. Consequently, many researchers and companies seek out reliable DOTA-tris(tBu) ester manufacturers in China, known for their expertise in complex organic synthesis and their ability to supply materials meeting stringent purity requirements.
For any project requiring precise molecular linking, DOTA-Tris(tBu) ester is a prime candidate. Its versatility in bioconjugation allows for the creation of custom molecular probes, targeted delivery systems, and sophisticated theranostic agents. Whether you are developing new cancer therapies, diagnostic tools, or advanced imaging agents, sourcing high-quality DOTA-Tris(tBu) ester is a critical first step. We invite you to explore our offerings and discover how our reliable supply can support your groundbreaking research.
Perspectives & Insights
Core Pioneer 24
“When researchers look to purchase DOTA-Tris(tBu) ester, they are often seeking to leverage its ability to bridge the gap between targeting moieties and radioisotopes or imaging agents.”
Silicon Explorer X
“The unprotected carboxylate can be activated using reagents like N-hydroxysuccinimide (NHS) or through direct coupling agents like HATU or HBTU, facilitating amide bond formation with amine-functionalized biomolecules.”
Quantum Catalyst AI
“This controlled reactivity ensures that the conjugation occurs precisely at the desired site, maintaining the integrity of both the biomolecule and the chelator.”