Discover the new Chem-Impex: Where innovation starts with a bond.

Catalog Number:
29716
CAS Number:
1263046-43-0
S-Fmoc-2-amino-5-(trityl-carbamoyl)-pentanoic acid
Purity:
≥ 99.5% (Chiral HPLC)
Synonym(s):
Fmoc-L-Homogln(Trt)-OH
Documents
$86.23 /25MG
Pack Size Availability Price
Request Bulk Quote
Product Information

(S)-Fmoc-2-amino-5-(trityl-carbamoyl)-pentanoic acid 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 trityl carbamoyl moiety enhances stability and solubility, making it an ideal choice for researchers focused on complex peptide structures.

In the pharmaceutical industry, (S)-Fmoc-2-amino-5-(trityl-carbamoyl)-pentanoic acid is particularly valuable for the development of peptide-based therapeutics, where precise control over amino acid sequences is crucial. Its unique structure allows for efficient coupling reactions, facilitating the synthesis of bioactive peptides with improved efficacy. Researchers appreciate its compatibility with various coupling reagents and its ability to yield high-purity products, making it a preferred choice for both academic and industrial applications.

Synonyms
Fmoc-L-Homogln(Trt)-OH
CAS Number
1263046-43-0
Purity
≥ 99.5% (Chiral HPLC)
Molecular Formula
C40H36N2O5
Molecular Weight
624.74
MDL Number
MFCD03093573
PubChem ID
75627352
Appearance
Off-white or white solid
Optical Rotation
[a]D20 = 1.5 ± 1 º (C=1 in MeOH)
Conditions
Store at 0 - 8 °C
General Information
Synonyms
Fmoc-L-Homogln(Trt)-OH
CAS Number
1263046-43-0
Purity
≥ 99.5% (Chiral HPLC)
Molecular Formula
C40H36N2O5
Molecular Weight
624.74
MDL Number
MFCD03093573
PubChem ID
75627352
Appearance
Off-white or white solid
Optical Rotation
[a]D20 = 1.5 ± 1 º (C=1 in MeOH)
Conditions
Store at 0 - 8 °C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

(S)-Fmoc-2-amino-5-(trityl-carbamoyl)-pentanoic acid 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. Its stability under various conditions makes it a preferred choice for researchers in organic chemistry.
  • Drug Development: In pharmaceutical research, it is used to create peptide-based drugs. The ability to modify the structure while maintaining biological activity is crucial for developing effective therapeutics.
  • Bioconjugation: The compound is employed in bioconjugation processes, where it helps attach biomolecules to surfaces or other molecules. This application is vital in creating targeted drug delivery systems.
  • Protein Engineering: Researchers utilize it in the design of novel proteins with enhanced properties. Its unique structure allows for the introduction of specific functionalities, improving protein stability and activity.
  • Analytical Chemistry: It is also used in analytical techniques to study protein interactions and dynamics. The compound's properties facilitate the development of assays that can provide insights into biological processes.

Citations