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Catalog Number:
11566
CAS Number:
68181-17-9
Ester N- hydroxyuccinimide de l'acide 3-(2-pyridyldithio)propionique
Purity:
≥ 97 % (HPLC)
Synonym(s):
N- Succinimidyl-3-(2-pyridyldithio)propionanate, Parti socialiste du travail (PSDP)
Documents
$100.05 /25 mg
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Product Information

Réactif de réticulation important pour la préparation de conjugués protéine-protéine et peptide-protéine liés par des liaisons disulfures.

Synonyms
N- Succinimidyl-3-(2-pyridyldithio)propionanate, Parti socialiste du travail (PSDP)
CAS Number
68181-17-9
Purity
≥ 97 % (HPLC)
Molecular Formula
C12H12N2O4S2
Molecular Weight
312.37
MDL Number
MFCD00009636
PubChem ID
100682
Appearance
Poudre blanche
Conditions
Conserver à 0-8 °C
General Information
Synonyms
N- Succinimidyl-3-(2-pyridyldithio)propionanate, Parti socialiste du travail (PSDP)
CAS Number
68181-17-9
Purity
≥ 97 % (HPLC)
Molecular Formula
C12H12N2O4S2
Molecular Weight
312.37
MDL Number
MFCD00009636
PubChem ID
100682
Appearance
Poudre blanche
Conditions
Conserver à 0-8 °C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

3-(2-Pyridyldithio)propionic acid N-hydroxyuccinimide ester is widely utilized in research focused on:

  • Bioconjugation: This compound serves as a versatile linker for attaching biomolecules, such as proteins or antibodies, to surfaces or other molecules, enhancing the development of targeted therapies in pharmaceuticals.
  • Drug Delivery Systems: Its ability to form stable conjugates makes it ideal for creating drug delivery vehicles that can improve the efficacy and specificity of treatments in cancer therapy.
  • Diagnostics: The compound is used in the development of diagnostic tools, such as biosensors, where it helps in the selective binding of analytes, leading to more accurate detection methods.
  • Material Science: In polymer chemistry, it aids in the synthesis of functionalized polymers, which can be used in coatings and adhesives, providing enhanced properties compared to traditional materials.
  • Research in Chemical Biology: It facilitates the study of protein interactions and cellular processes, enabling researchers to explore biological mechanisms with greater precision.

Citations