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Catalog Number:
12403
CAS Number:
178924-05-5
Ácido N α - Fmoc- N β -aliloxicarbonil-D-2,3-diaminopropiónico
Purity:
≥ 99 % (HPLC)
Synonym(s):
Fmoc-D-Dap(Aloc)-OH
Documents
$86.23 /250 mg
Tamaño
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Product Information

Na-Fmoc-Nb-allyloxycarbonyl-D-2,3-diaminopropionic acid is a versatile building block 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 acids during the synthesis of complex peptides. Its unique structure, including the allyloxycarbonyl group, enhances its reactivity and stability, making it an ideal choice for researchers looking to create tailored peptides with specific functionalities.

In the pharmaceutical industry, Na-Fmoc-Nb-allyloxycarbonyl-D-2,3-diaminopropionic acid plays a crucial role in the development of therapeutic peptides, enabling the synthesis of bioactive compounds with improved efficacy and reduced side effects. Its application extends to various fields, including biotechnology and materials science, where it can be employed in the design of novel biomaterials and drug delivery systems. The compound's ability to facilitate efficient coupling reactions and its compatibility with automated synthesizers make it a preferred choice for both academic and industrial laboratories.

Synonyms
Fmoc-D-Dap(Aloc)-OH
CAS Number
178924-05-5
Purity
≥ 99 % (HPLC)
Molecular Formula
C22H22N2O6
Molecular Weight
410.53
MDL Number
MFCD01076137
PubChem ID
3662877
Melting Point
142-152 °C
Appearance
Polvo cristalino blanco
Optical Rotation
[a] D 20 = +10 ± 2º (C=1 en MeOH)
Conditions
Conservar entre 0 y 8 °C.
General Information
Synonyms
Fmoc-D-Dap(Aloc)-OH
CAS Number
178924-05-5
Purity
≥ 99 % (HPLC)
Molecular Formula
C22H22N2O6
Molecular Weight
410.53
MDL Number
MFCD01076137
PubChem ID
3662877
Melting Point
142-152 °C
Appearance
Polvo cristalino blanco
Optical Rotation
[a] D 20 = +10 ± 2º (C=1 en MeOH)
Conditions
Conservar entre 0 y 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-allyloxycarbonyl-D-2,3-diaminopropionic acid is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protecting group in the synthesis of peptides, allowing for selective reactions without interfering with other functional groups. This is crucial in developing complex peptides for pharmaceuticals.
  • Drug Development: Its role in creating modified amino acids enhances the properties of peptide-based drugs, improving their efficacy and stability, which is vital for the pharmaceutical industry.
  • Bioconjugation: The compound can be used in bioconjugation techniques, facilitating the attachment of biomolecules to surfaces or other molecules, which is important in diagnostics and therapeutic applications.
  • Research in Neuroscience: By incorporating this compound into peptide sequences, researchers can explore neuropeptides and their functions, contributing to advancements in understanding neurological disorders.
  • Custom Synthesis: Its versatility allows for tailored synthesis of novel compounds, meeting specific research needs in various fields, including materials science and biochemistry.

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