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Catalog Number:
37062
CAS Number:
176755-00-3
Ácido N α -Aliloxicarbonil- N β -Fmoc-L-2,3-diaminopropiónico
Purity:
≥ 99 % (HPLC)
Synonym(s):
Aloc-L-Dap(Fmoc)-OH
Documents
$58.39 /100 mg
Tamaño
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Product Information

Na-Allyloxycarbonyl-Nb-Fmoc-L-2,3-diaminopropionic acid is a versatile compound widely utilized in peptide synthesis and drug development. This amino acid derivative features a unique allyloxycarbonyl protecting group, which enhances its stability and reactivity, making it an ideal choice for researchers focused on the synthesis of complex peptides. Its Fmoc (Fluorenylmethyloxycarbonyl) group allows for easy deprotection under mild conditions, facilitating streamlined processes in laboratory settings.

This compound is particularly valuable in the pharmaceutical industry for the development of peptide-based therapeutics, where precise control over amino acid sequences is crucial. Its application extends to the synthesis of bioactive peptides, which are essential in various biological functions and therapeutic interventions. Researchers can leverage its unique properties to create innovative solutions in drug design, enhancing the efficacy and specificity of therapeutic agents. With its robust profile, Na-Allyloxycarbonyl-Nb-Fmoc-L-2,3-diaminopropionic acid stands out as a critical tool for advancing peptide chemistry and biopharmaceutical development.

Synonyms
Aloc-L-Dap(Fmoc)-OH
CAS Number
176755-00-3
Purity
≥ 99 % (HPLC)
Molecular Formula
C22H22N2O6
Molecular Weight
410.4
PubChem ID
123682670
Melting Point
173 - 175 °C
Appearance
Polvo cristalino blanco
Optical Rotation
[a] D 20 = -9 ± 2 ° (C=1 en MeOH)
Conditions
Conservar entre 2 y 8 °C.
General Information
Synonyms
Aloc-L-Dap(Fmoc)-OH
CAS Number
176755-00-3
Purity
≥ 99 % (HPLC)
Molecular Formula
C22H22N2O6
Molecular Weight
410.4
PubChem ID
123682670
Melting Point
173 - 175 °C
Appearance
Polvo cristalino blanco
Optical Rotation
[a] D 20 = -9 ± 2 ° (C=1 en MeOH)
Conditions
Conservar entre 2 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 -Allyloxycarbonyl- Nb -Fmoc-L-2,3-diaminopropionic acid is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, particularly for creating complex structures in pharmaceutical research.
  • Drug Development: Its unique functional groups enhance the solubility and stability of drug candidates, making it valuable in the formulation of new medications.
  • Bioconjugation: The compound is effective in bioconjugation processes, allowing researchers to attach biomolecules to surfaces or other compounds, which is crucial in diagnostics and therapeutic applications.
  • Proteomics: It plays a significant role in proteomics research by aiding in the modification and analysis of proteins, helping scientists understand protein interactions and functions.
  • Research in Material Science: The chemical can be used to create functionalized materials, enhancing properties such as biocompatibility and reactivity, which are essential in developing advanced materials for various applications.

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