4-nitrophenyl 2-(pyridin-2-yldisulfanyl)ethyl carbonate

≥95%

  • Product Code: 119530
  CAS:    874302-76-8
Molecular Weight: 352.39 g./mol Molecular Formula: C₁₄H₁₂N₂O₅S₂
EC Number: MDL Number: MFCD28556879
Melting Point: Boiling Point:
Density: Storage Condition: 2-8°C, store under inert gas
Product Description: This chemical is widely used in biochemical research, particularly in the study of protein interactions and modifications. It serves as a versatile reagent for introducing disulfide bonds or pyridyl disulfide groups into molecules, enabling the controlled conjugation of proteins or peptides. Its application is crucial in the development of drug delivery systems, where it facilitates the creation of targeted therapies by linking therapeutic agents to carriers. Additionally, it is employed in the synthesis of bioconjugates for diagnostic assays, enhancing the sensitivity and specificity of detection methods. Its ability to form reversible disulfide bonds makes it valuable in designing stimuli-responsive materials for biomedical applications.
Product Specification:
Test Specification
Appearance Solid
Purity (%) 94.5-100
Infrared Spectrum Conforms To Structure
NMR Conforms To Structure
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.100 10-20 days ฿15,340.00
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-
0.250 10-20 days ฿27,630.00
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-
1.000 10-20 days ฿67,200.00
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-
4-nitrophenyl 2-(pyridin-2-yldisulfanyl)ethyl carbonate
This chemical is widely used in biochemical research, particularly in the study of protein interactions and modifications. It serves as a versatile reagent for introducing disulfide bonds or pyridyl disulfide groups into molecules, enabling the controlled conjugation of proteins or peptides. Its application is crucial in the development of drug delivery systems, where it facilitates the creation of targeted therapies by linking therapeutic agents to carriers. Additionally, it is employed in the synthesis of bioconjugates for diagnostic assays, enhancing the sensitivity and specificity of detection methods. Its ability to form reversible disulfide bonds makes it valuable in designing stimuli-responsive materials for biomedical applications.
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