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

Catalog Number:
47702
CAS Number:
2389078-45-7
Na-Fmoc-Nb-Alloc-Nb-methyl-L-2,3-diaminopropionic acid
Purity:
≥ 98% (HPLC)
Synonym(s):
Fmoc-Dap(Aloc,Me)-OH
Documents
$230.00 /25MG
Pack Size Availability Price
Request Bulk Quote
Product Information

Na-Fmoc-Nb-Alloc-Nb-methyl-L-2,3-diaminopropionic acid is a versatile amino acid derivative that plays a crucial role in peptide synthesis and drug development. This compound features a fluorenylmethoxycarbonyl (Fmoc) protecting group, which is widely recognized for its stability and ease of removal, making it an ideal choice for solid-phase peptide synthesis. The presence of the Alloc (allyloxycarbonyl) group further enhances its utility in selective deprotection strategies, allowing for the precise manipulation of peptide sequences. Researchers and industry professionals can leverage this compound in the synthesis of complex peptides and biologically active molecules, facilitating advancements in therapeutic development and biomolecular research.

This compound is particularly beneficial in the field of medicinal chemistry, where its unique structure allows for the incorporation of diverse functionalities into peptide chains. Its application extends to the development of peptide-based drugs, where the ability to fine-tune the peptide structure can lead to improved efficacy and specificity. With its robust properties and practical applications, Na-Fmoc-Nb-Alloc-Nb-methyl-L-2,3-diaminopropionic acid stands out as a valuable tool for researchers aiming to innovate in peptide synthesis and drug discovery.

Synonyms
Fmoc-Dap(Aloc,Me)-OH
CAS Number
2389078-45-7
Purity
≥ 98% (HPLC)
Molecular Formula
C23H24N2O6
Molecular Weight
424.5
Appearance
White powder
Optical Rotation
[a]D20 = -16.5 - 19.5 °(C=1 in MeOH)
Conditions
Store at 2 - 8 °C
General Information
Synonyms
Fmoc-Dap(Aloc,Me)-OH
CAS Number
2389078-45-7
Purity
≥ 98% (HPLC)
Molecular Formula
C23H24N2O6
Molecular Weight
424.5
Appearance
White powder
Optical Rotation
[a]D20 = -16.5 - 19.5 °(C=1 in MeOH)
Conditions
Store at 2 - 8 °C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

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

  • Peptide Synthesis: This compound serves as a versatile building block in the synthesis of peptides, allowing researchers to create complex structures with specific biological activities.
  • Drug Development: It plays a crucial role in the pharmaceutical industry for developing novel therapeutics, particularly in designing peptide-based drugs that can target specific diseases.
  • Bioconjugation: The compound is used in bioconjugation processes, facilitating the attachment of biomolecules to surfaces or other molecules, which is essential in creating targeted drug delivery systems.
  • Research in Neuroscience: It is applied in studies related to neuropeptides, helping researchers understand the role of peptides in neurological functions and disorders.
  • Protein Engineering: This chemical aids in the modification of proteins, enhancing their stability and functionality, which is vital for various applications in biotechnology and synthetic biology.

Citations