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Catalog Number:
23171
CAS Number:
112725-22-1
Succinimidyl 3-(tri-n-butylstannyl)benzoate
Purity:
≥ 98% (NMR)
Documents
$110.00 /25MG
Pack Size Availability Price
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Product Information

Succinimidyl 3-(tri-n-butylstannyl)benzoate is a versatile compound widely utilized in the fields of organic synthesis and bioconjugation. This compound features a succinimidyl group that enhances its reactivity, making it an excellent choice for coupling reactions with amines and other nucleophiles. Its tri-n-butylstannyl moiety not only provides stability but also facilitates the introduction of the benzoate group into various substrates, which is particularly beneficial in the development of targeted drug delivery systems and in the synthesis of complex biomolecules.

Researchers and industry professionals can leverage this compound for applications in medicinal chemistry, where it serves as a key intermediate in the synthesis of pharmaceuticals and biologically active compounds. Additionally, its unique properties allow for the functionalization of surfaces in materials science, enhancing the performance of coatings and polymers. The ability to easily incorporate this compound into various chemical reactions makes it a valuable tool for advancing research and development in multiple sectors.

CAS Number
112725-22-1
Purity
≥ 98% (NMR)
Molecular Formula
C23H35NSnO4
Molecular Weight
508.22
MDL Number
MFCD01863152
PubChem ID
130716
Appearance
Syrupy oil
Conditions
Store at 0 - 8 °
General Information
CAS Number
112725-22-1
Purity
≥ 98% (NMR)
Molecular Formula
C23H35NSnO4
Molecular Weight
508.22
MDL Number
MFCD01863152
PubChem ID
130716
Appearance
Syrupy oil
Conditions
Store at 0 - 8 °
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Succinimidyl 3-(tri-n-butylstannyl)benzoate is widely utilized in research focused on:

  • Bioconjugation: This compound serves as a versatile linker in bioconjugation processes, allowing researchers to attach biomolecules to surfaces or other molecules, enhancing the development of targeted drug delivery systems.
  • Protein Labeling: It is used in the labeling of proteins for various applications, including imaging and tracking in biological studies, which helps in understanding protein interactions and functions.
  • Polymer Chemistry: The compound is employed in the synthesis of organotin-containing polymers, which are valuable in creating materials with unique properties, such as improved thermal stability and mechanical strength.
  • Diagnostics: In the field of diagnostics, it aids in the development of assays and sensors, providing enhanced sensitivity and specificity in detecting biomolecules, crucial for early disease diagnosis.
  • Environmental Applications: Its properties are leveraged in environmental chemistry for the detection and remediation of pollutants, offering a method to address contamination issues effectively.

Citations