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Catalog Number:
12608
CAS Number:
654670-89-0
Nα-Fmoc-Nβ-4-methyltrityl-L-2,3-diaminopropionic acid
Purity:
≥ 98% (HPLC)
Synonym(s):
Fmoc-L-Dap(Mtt)-OH
Documents
$88.63 /250MG
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Product Information

Na-Fmoc-Nb-4-methyltrityl-L-2,3-diaminopropionic acid is a versatile amino acid derivative widely utilized in peptide synthesis and drug development. This compound features a protective Fmoc (9-fluorenylmethoxycarbonyl) group, which allows for selective deprotection during the synthesis process, making it an essential building block for creating complex peptides. Its unique structure, including the 4-methyltrityl group, enhances stability and solubility, facilitating smoother reactions and higher yields. Researchers and industry professionals can leverage this compound in the development of therapeutic peptides, particularly in the fields of oncology and immunology, where precise amino acid sequences are crucial for efficacy.

The compound's ability to provide a robust framework for peptide synthesis, combined with its favorable properties, positions it as a preferred choice among chemists. Its application extends to the creation of novel drug candidates, where the incorporation of specific amino acids can lead to improved pharmacological profiles. With its proven track record in research and development, Na-Fmoc-Nb-4-methyltrityl-L-2,3-diaminopropionic acid stands out as a valuable asset for those aiming to innovate in peptide-based therapies.

Synonyms
Fmoc-L-Dap(Mtt)-OH
CAS Number
654670-89-0
Purity
≥ 98% (HPLC)
Molecular Formula
C38H34N2O4
Molecular Weight
582.7
MDL Number
MFCD02094097
PubChem ID
75210720
Appearance
White to off-white crystalline powder
Optical Rotation
[a]D20 = +11.0 to +13.5 ° (C=1 in MeOH)
Conditions
Store at 0 - 8 °C
General Information
Synonyms
Fmoc-L-Dap(Mtt)-OH
CAS Number
654670-89-0
Purity
≥ 98% (HPLC)
Molecular Formula
C38H34N2O4
Molecular Weight
582.7
MDL Number
MFCD02094097
PubChem ID
75210720
Appearance
White to off-white crystalline powder
Optical Rotation
[a]D20 = +11.0 to +13.5 ° (C=1 in MeOH)
Conditions
Store at 0 - 8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Na-Fmoc-Nb-4-methyltrityl-L-2,3-diaminopropionic acid is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a crucial building block in the synthesis of peptides, allowing researchers to create complex structures with specific functionalities.
  • Drug Development: Its unique properties make it valuable in the pharmaceutical industry for designing novel therapeutic agents, particularly in targeting specific biological pathways.
  • Bioconjugation: The compound is employed in bioconjugation processes, facilitating the attachment of biomolecules to surfaces or other molecules, which is essential in developing biosensors and targeted drug delivery systems.
  • Research in Protein Engineering: It is used in protein engineering studies to modify amino acid sequences, helping scientists understand protein function and stability better.
  • Material Science: The chemical finds applications in creating advanced materials, particularly in the development of polymers with tailored properties for specific applications.

Citations