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Catalog Number:
05698
CAS Number:
200926-18-7
N α,im -Bis-Fmoc-D-histidina
Purity:
≥ 98 % (TLC)
Synonym(s):
Fmoc-D-His(Fmoc)-OH
Documents
$65.40 /250 mg
Tamaño
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Información del producto

Na,im-Bis-Fmoc-D-histidine is a versatile amino acid derivative that plays a crucial role in peptide synthesis and drug development. This compound is particularly valued in the field of biochemistry and pharmaceutical research due to its ability to enhance the stability and solubility of peptides. Its unique structure, featuring two Fmoc (fluorenylmethyloxycarbonyl) protecting groups, allows for selective deprotection, making it an ideal choice for synthesizing complex peptides with high purity and yield. Researchers often utilize Na,im-Bis-Fmoc-D-histidine in the development of peptide-based therapeutics, where precise control over amino acid sequences is essential for achieving desired biological activity.

In addition to its applications in peptide synthesis, Na,im-Bis-Fmoc-D-histidine is also used in the study of protein interactions and enzyme activity. Its ability to mimic natural histidine residues makes it a valuable tool for probing biological mechanisms and developing novel biomolecules. The compound's stability under various conditions further enhances its utility in laboratory settings, providing researchers with a reliable building block for their studies. With its broad range of applications and significant advantages over similar compounds, Na,im-Bis-Fmoc-D-histidine is an essential addition to any researcher's toolkit.

Número CAS
200926-18-7
Fórmula molecular
C36H29N3O6
Peso molecular
599.6
Número MDL
MFCD00077057
Punto de fusión
160 - 161 °C
Rotación óptica
[a] D 20 = +5 ± 1º (C=1 en DMF)
Condiciones
Conservar entre 0 y 8 °C.
Información general
Número CAS
200926-18-7
Fórmula molecular
C36H29N3O6
Peso molecular
599.6
Número MDL
MFCD00077057
Punto de fusión
160 - 161 °C
Rotación óptica
[a] D 20 = +5 ± 1º (C=1 en DMF)
Condiciones
Conservar entre 0 y 8 °C.
Propiedades
¡Pronto habrá más información sobre la propiedad!
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Seguridad y normativas
Materiales peligrosos
-
Antibiótico
-
Regulado por la DEA
No
Advertencias
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Aplicaciones

Na,im-Bis-Fmoc-D-histidine is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protecting group in the synthesis of peptides, allowing for the selective modification of amino acids. Its stability under various conditions makes it a preferred choice for researchers in organic chemistry.
  • Drug Development: In pharmaceutical research, it is used to create histidine-containing compounds that can enhance drug efficacy and stability, particularly in formulations targeting specific biological pathways.
  • Bioconjugation: The compound is instrumental in bioconjugation processes, where it helps attach biomolecules to surfaces or other molecules, facilitating the development of targeted therapies and diagnostics.
  • Protein Engineering: Researchers utilize it in the design of proteins with enhanced properties, such as increased solubility or stability, which is crucial for therapeutic applications and industrial enzymes.
  • Analytical Chemistry: It is used in the development of analytical methods for detecting and quantifying histidine derivatives, providing valuable insights in both academic and industrial laboratories.

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