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Catalog Number:
27868
CAS Number:
276869-41-1
Fmoc-Asu(OtBu)-OH
Purity:
≥ 97% (HPLC)
Documents
$120.88 /25MG
Pack Size Availability Price
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Product Information

Fmoc-Asu(OtBu)-OH is a versatile amino acid derivative widely utilized in peptide synthesis and drug development. This compound features a fluorenylmethoxycarbonyl (Fmoc) protecting group, which is essential for the selective protection of amino groups during the synthesis of peptides. Its unique structure, including the tert-butyl (OtBu) ester, enhances solubility and stability, making it an ideal choice for researchers looking to streamline their synthesis processes.

In practical applications, Fmoc-Asu(OtBu)-OH is particularly valuable in the pharmaceutical industry for the development of peptide-based therapeutics. Its ability to facilitate the formation of complex peptide sequences allows for the exploration of novel drug candidates. Additionally, the compound's stability under various reaction conditions ensures high yields and purity, which are critical for successful research outcomes. Researchers benefit from its ease of use and compatibility with standard coupling reagents, making it a preferred choice for both academic and industrial applications.

CAS Number
276869-41-1
Purity
≥ 97% (HPLC)
Molecular Formula
C27H33NO6
Molecular Weight
467.56
MDL Number
MFCD00080269
PubChem ID
69297251
Appearance
White to off-white powder
Optical Rotation
[a]D20 = -11 ± 2º (C=1 in DMF)
Conditions
Store at 0-8 °C
General Information
CAS Number
276869-41-1
Purity
≥ 97% (HPLC)
Molecular Formula
C27H33NO6
Molecular Weight
467.56
MDL Number
MFCD00080269
PubChem ID
69297251
Appearance
White to off-white powder
Optical Rotation
[a]D20 = -11 ± 2º (C=1 in DMF)
Conditions
Store at 0-8 °C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Fmoc-Asu(OtBu)-OH is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protecting group in solid-phase peptide synthesis, allowing for the selective modification of amino acids without interfering with the overall peptide structure.
  • Drug Development: It is used in the design of peptide-based therapeutics, providing a stable framework for developing new drugs that target specific biological pathways.
  • Bioconjugation: The compound facilitates the attachment of peptides to various biomolecules, enhancing the efficacy of drug delivery systems and diagnostic agents.
  • Research in Biochemistry: It aids researchers in studying protein interactions and functions by enabling the synthesis of modified peptides that can mimic natural substrates.
  • Custom Peptide Libraries: Fmoc-Asu(OtBu)-OH is essential for creating diverse peptide libraries for screening potential drug candidates, allowing for rapid identification of effective compounds.

Citations