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Catalog Number:
07055
CAS Number:
251317-00-7
Ácido N α - Fmoc-D-2,3-diaminopropiónico
Purity:
≥ 99,5 % (HPLC quiral)
Synonym(s):
Fmoc-D-Dap-OH
Documents
$65.40 /250 mg
Tamaño
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Product Information

Na-Fmoc-D-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 enhances solubility and stability, facilitating its application in various biochemical and pharmaceutical research settings. Researchers appreciate its role in developing therapeutics, particularly in the fields of oncology and immunology, where precise peptide sequences are crucial for efficacy.

In addition to its applications in peptide synthesis, Na-Fmoc-D-2,3-diaminopropionic acid is also valuable in the study of protein interactions and enzyme activity. Its ability to form stable linkages with other amino acids allows for the exploration of novel peptide-based drugs and biomaterials. With its favorable properties and broad applicability, this compound stands out as a key ingredient for professionals seeking to innovate in peptide chemistry and drug formulation.

Synonyms
Fmoc-D-Dap-OH
CAS Number
251317-00-7
Purity
≥ 99,5 % (HPLC quiral)
Molecular Formula
C18H18N2O4
Molecular Weight
326.3
MDL Number
MFCD01318733
PubChem ID
5165519
Melting Point
> 135 °C (descenso)
Appearance
Polvo de color blanco a blanquecino
Optical Rotation
[a] 20 D = +27 ± 2º (C=1 en 4 ml de MeOH + 1 ml de HCl 1N)
Conditions
Conservar entre 0 y 8 °C.
General Information
Synonyms
Fmoc-D-Dap-OH
CAS Number
251317-00-7
Purity
≥ 99,5 % (HPLC quiral)
Molecular Formula
C18H18N2O4
Molecular Weight
326.3
MDL Number
MFCD01318733
PubChem ID
5165519
Melting Point
> 135 °C (descenso)
Appearance
Polvo de color blanco a blanquecino
Optical Rotation
[a] 20 D = +27 ± 2º (C=1 en 4 ml de MeOH + 1 ml de HCl 1N)
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-D-2,3-diaminopropionic acid is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as an important building block in the synthesis of peptides, particularly in solid-phase peptide synthesis, allowing for the creation of complex and functional peptides.
  • Drug Development: It is used in the design of novel pharmaceuticals, especially in creating peptide-based drugs that can target specific biological pathways, enhancing therapeutic efficacy.
  • Bioconjugation: The chemical is valuable in bioconjugation processes, where it helps attach biomolecules to surfaces or other molecules, improving the delivery and effectiveness of drugs.
  • Research in Neuroscience: Its derivatives are explored in studies related to neuropeptides, aiding researchers in understanding neurological functions and potential treatments for disorders.
  • Protein Engineering: This compound is utilized in engineering proteins with enhanced stability and functionality, which is critical in biotechnology and industrial applications.

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