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Catalog Number:
47707
CAS Number:
946849-80-5
Fmoc-Cystamine-Suc-OH
Purity:
≥ 98% (HPLC)
Synonym(s):
Succinoyl-Fmoc-Cystamine
Documents
$50.00 /25MG
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Product Information

Fmoc-Cystamine-Suc-OH is a versatile compound widely utilized in peptide synthesis and bioconjugation applications. This compound features a unique Fmoc (fluorenylmethyloxycarbonyl) protecting group, which is essential for the selective protection of amines during the synthesis of peptides. Its disulfide bond provides stability and facilitates the formation of complex structures, making it an ideal choice for researchers focused on developing novel peptides and proteins.

In the pharmaceutical and biotechnology industries, Fmoc-Cystamine-Suc-OH is particularly valuable for creating targeted drug delivery systems and studying protein interactions. Its ability to form stable conjugates with various biomolecules enhances its utility in drug development and therapeutic applications. Additionally, this compound can be employed in the design of biosensors and diagnostic tools, showcasing its broad relevance in both academic research and industrial applications. With its unique properties and practical uses, Fmoc-Cystamine-Suc-OH stands out as a crucial tool for advancing research in peptide chemistry and bioconjugation.

Synonyms
Succinoyl-Fmoc-Cystamine
CAS Number
946849-80-5
Purity
≥ 98% (HPLC)
Molecular Formula
C23H26N2O5S2
Molecular Weight
474.6
MDL Number
MFCD35058470
PubChem ID
156594890
Appearance
White crystalline powder
Conditions
Store at 2 - 8 °C
General Information
Synonyms
Succinoyl-Fmoc-Cystamine
CAS Number
946849-80-5
Purity
≥ 98% (HPLC)
Molecular Formula
C23H26N2O5S2
Molecular Weight
474.6
MDL Number
MFCD35058470
PubChem ID
156594890
Appearance
White crystalline powder
Conditions
Store at 2 - 8 °C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Fmoc-Cystamine-Suc-OH is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protecting group in the synthesis of peptides, allowing for the selective modification of amino acids while ensuring stability during chemical reactions.
  • Drug Development: It plays a crucial role in the design of novel pharmaceuticals, particularly in creating disulfide linkages that enhance the stability and efficacy of drug candidates.
  • Bioconjugation: Researchers use it to facilitate the attachment of biomolecules, such as proteins or nucleic acids, to surfaces or other molecules, improving the functionality of biosensors and drug delivery systems.
  • Antioxidant Research: The compound is studied for its potential antioxidant properties, which can be beneficial in developing treatments for oxidative stress-related diseases.
  • Nanotechnology: It is applied in the fabrication of nanomaterials, where its unique chemical properties contribute to the development of targeted drug delivery systems and advanced materials.

Citations