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Catalog Number:
06074
CAS Number:
133367-32-5
N im -4-méthyltrityl-L-histidine
Purity:
≥ 99 % (CCM)
Synonym(s):
L-His(Mtt)-OH
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Informations sur le produit

Nim-4-Methyltrityl-L-histidine is a sophisticated amino acid derivative that plays a pivotal role in biochemical research and pharmaceutical applications. This compound is recognized for its unique structure, featuring a 4-methylphenyl-diphenylmethyl group, which enhances its stability and solubility in various solvents. Researchers utilize Nim-4-Methyltrityl-L-histidine primarily in peptide synthesis and as a building block for the development of novel therapeutic agents. Its ability to facilitate the formation of complex structures makes it invaluable in the design of targeted drug delivery systems and in the study of protein interactions.

In addition to its applications in drug development, Nim-4-Methyltrityl-L-histidine is also employed in the synthesis of biologically active compounds, contributing to advancements in medicinal chemistry. Its unique properties allow for improved efficacy and selectivity in therapeutic applications, making it a preferred choice among professionals in the pharmaceutical and biotechnological sectors. With its potential to enhance research outcomes and streamline synthesis processes, Nim-4-Methyltrityl-L-histidine stands out as a key compound for those looking to innovate in the field.

Numéro CAS 
133367-32-5
Formule moléculaire
C26H25N3O2
Poids moléculaire 
411.51
Point de fusion 
203-216 °C
Rotation optique 
[a] D 24 = +28 ± 2º (C = 1 % dans l'acide acétique)
Informations générales
Numéro CAS 
133367-32-5
Formule moléculaire
C26H25N3O2
Poids moléculaire 
411.51
Point de fusion 
203-216 °C
Rotation optique 
[a] D 24 = +28 ± 2º (C = 1 % dans l'acide acétique)
Propriétés
Informations complémentaires sur la propriété à venir prochainement !
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Sécurité et réglementation
Matières dangereuses
-
Antibiotique
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Réglementé par la DEA
Non
Avertissements 
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Applications

Nim-4-Methyltrityl-L-histidine is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, which are essential in drug development and biotechnology.
  • Bioconjugation: It is used in bioconjugation processes to attach biomolecules to surfaces or other molecules, enhancing the efficacy of targeted therapies.
  • Drug Discovery: Researchers employ this compound in screening assays to identify potential drug candidates, particularly in oncology and immunology.
  • Protein Engineering: Its unique structure allows for modifications in protein engineering, leading to the development of novel therapeutic proteins with improved properties.
  • Diagnostics: The compound is also explored in the development of diagnostic tools, aiding in the detection of diseases through biomarker identification.

Citations