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Catalog Number:
14437
CAS Number:
882847-27-0
Fmoc- N -[2-(tritylmercapto)éthyl]glycine
Purity:
≥ 98 % (HPLC)
Synonym(s):
Fmoc- N -[2-(tritylmercapto)éthyl]-Gly-OH, Fmoc-Nhomocys(Trt)-OH
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$132.80 /25 mg
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Product Information

Fmoc-N-[2-(tritylmercapto)ethyl]glycine is a versatile building block widely utilized in peptide synthesis and pharmaceutical research. This compound features a protective Fmoc (9-fluorenylmethyloxycarbonyl) group, which is essential for the selective protection of amino groups during the synthesis of peptides. Its unique tritylmercaptoethyl side chain enhances its stability and solubility, making it an ideal choice for researchers working on complex peptide sequences.

In practical applications, Fmoc-N-[2-(tritylmercapto)ethyl]glycine is particularly valuable in the development of peptide-based therapeutics and in the study of protein interactions. Its ability to facilitate the synthesis of modified peptides allows for the exploration of new drug candidates and the optimization of existing ones. Researchers benefit from its high purity and reliability, ensuring consistent results in their experiments. This compound stands out in the field of medicinal chemistry for its efficiency in producing high-quality peptides, paving the way for advancements in drug discovery and development.

Synonyms
Fmoc- N -[2-(tritylmercapto)éthyl]-Gly-OH, Fmoc-Nhomocys(Trt)-OH
CAS Number
882847-27-0
Purity
≥ 98 % (HPLC)
Molecular Formula
C 38 H 33 NON 4 S
Molecular Weight
599.74
MDL Number
MFCD08457837
PubChem ID
17040132
Melting Point
156 - 163 °C
Appearance
Solide blanc
Conditions
Conserver à 0 - 8 °C
General Information
Synonyms
Fmoc- N -[2-(tritylmercapto)éthyl]-Gly-OH, Fmoc-Nhomocys(Trt)-OH
CAS Number
882847-27-0
Purity
≥ 98 % (HPLC)
Molecular Formula
C 38 H 33 NON 4 S
Molecular Weight
599.74
MDL Number
MFCD08457837
PubChem ID
17040132
Melting Point
156 - 163 °C
Appearance
Solide blanc
Conditions
Conserver à 0 - 8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

Fmoc-N-[2-(tritylmercapto)ethyl]glycine is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a valuable building block in solid-phase peptide synthesis, allowing researchers to create complex peptides with high purity and yield.
  • Drug Development: Its unique structure aids in the design of novel pharmaceuticals, particularly in developing targeted therapies that require specific amino acid sequences.
  • Bioconjugation: The compound can be employed in bioconjugation processes, facilitating the attachment of biomolecules to surfaces or other compounds, which is crucial in diagnostics and therapeutic applications.
  • Research in Proteomics: It is used in proteomics studies to modify proteins, helping scientists understand protein interactions and functions better.
  • Material Science: The chemical's properties make it suitable for creating advanced materials with specific functionalities, such as drug delivery systems or biosensors.

Citations