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Catalog Number:
23153
CAS Number:
169751-10-4
Sulfosuccinimidyl 6-[3-(2-pyridyldithio)propionamido]hexanoate
Purity:
≥ 98% (Elemental Analysis)
Synonym(s):
sulfo-LC-SPDP
Documents
$450.00 /50MG
Pack Size Availability Price
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Product Information

Sulfosuccinimidyl 6-[3-(2-pyridyldithio)propionamido]hexanoate is a versatile compound widely utilized in bioconjugation and protein labeling applications. This compound features a unique pyridyldithio moiety, which allows for selective and stable conjugation to thiol-containing biomolecules, making it an essential tool for researchers in the fields of biochemistry and molecular biology. Its ability to form disulfide bonds enhances the stability of conjugates, facilitating the development of targeted drug delivery systems and diagnostic agents.

In addition to its applications in research, this compound is particularly valuable in the development of biotherapeutics, where precise labeling of proteins is crucial for tracking and studying biological processes. The sulfosuccinimidyl group ensures efficient coupling to amine groups, providing a reliable method for creating stable conjugates. Researchers can leverage this compound to enhance the efficacy of their studies, improve the specificity of assays, and develop innovative solutions in drug development and diagnostics.

Synonyms
sulfo-LC-SPDP
CAS Number
169751-10-4
Purity
≥ 98% (Elemental Analysis)
Molecular Formula
C18H22N3S3O8Na
Molecular Weight
527.56
MDL Number
MFCD00083162
PubChem ID
4588467
Appearance
Off-white to tan powder
Conditions
Store at 0-8 °C
General Information
Synonyms
sulfo-LC-SPDP
CAS Number
169751-10-4
Purity
≥ 98% (Elemental Analysis)
Molecular Formula
C18H22N3S3O8Na
Molecular Weight
527.56
MDL Number
MFCD00083162
PubChem ID
4588467
Appearance
Off-white to tan powder
Conditions
Store at 0-8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Sulfosuccinimidyl 6-[3-(2-pyridyldithio)propionamido]hexanoate is widely utilized in research focused on:

  • Bioconjugation: This compound is essential for attaching biomolecules, such as proteins or antibodies, to surfaces or other molecules, enhancing the development of targeted therapies and diagnostics.
  • Drug Delivery Systems: Its ability to form stable conjugates makes it valuable in creating drug delivery systems that improve the efficacy and specificity of therapeutic agents, particularly in cancer treatments.
  • Protein Labeling: Researchers use this chemical for labeling proteins with fluorescent tags, allowing for real-time tracking of protein interactions and cellular processes in live cells.
  • Diagnostics: It plays a crucial role in the development of diagnostic assays, particularly in immunoassays, by facilitating the attachment of detection molecules to antigens.
  • Research on Redox Biology: The unique disulfide bond in this compound allows scientists to study redox reactions and cellular signaling pathways, contributing to advancements in understanding various diseases.

Citations