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Catalog Number:
04053
CAS Number:
60142-89-4
Acide boc-7-aminoheptanoïque
Purity:
≥ 98 % (HPLC)
Synonym(s):
Boc-7-Ahp-OH
Documents
$20.20 /1G
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Informations sur le produit

Boc-7-aminoheptanoic acid is a versatile amino acid derivative widely utilized in peptide synthesis and pharmaceutical research. This compound features a tert-butoxycarbonyl (Boc) protecting group, which enhances its stability and reactivity, making it an ideal choice for the formation of complex peptides. Its unique structure allows for selective reactions, facilitating the incorporation of this amino acid into various peptide sequences. Researchers appreciate its role in developing bioactive peptides and drug candidates, particularly in the fields of medicinal chemistry and biochemistry.

The practical applications of Boc-7-aminoheptanoic acid extend to the synthesis of peptide-based therapeutics, where it serves as a building block for creating compounds with enhanced biological activity. Its ability to improve solubility and stability in formulations makes it a valuable asset in drug development. Additionally, this compound can be employed in the design of targeted delivery systems, contributing to advancements in personalized medicine. With its favorable properties and broad applicability, Boc-7-aminoheptanoic acid is an essential tool for researchers and industry professionals aiming to innovate in the realm of peptide synthesis and drug discovery.

Numéro CAS 
60142-89-4
Formule moléculaire
C 12 H 23 NON 4
Poids moléculaire 
245.3
Point de fusion 
53 - 58 °C
Rotation optique 
[a] 20 D = -1 ± 0,5 ° (C = 1,1 dans MeOH)
Informations générales
Numéro CAS 
60142-89-4
Formule moléculaire
C 12 H 23 NON 4
Poids moléculaire 
245.3
Point de fusion 
53 - 58 °C
Rotation optique 
[a] 20 D = -1 ± 0,5 ° (C = 1,1 dans MeOH)
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

Boc-7-aminoheptanoic acid is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protective group in the synthesis of peptides, allowing for the selective modification of amino acids without affecting the overall structure.
  • Drug Development: It is used in the design of pharmaceutical compounds, particularly in creating bioactive peptides that can target specific biological pathways.
  • Bioconjugation: The compound facilitates the attachment of biomolecules, such as proteins or antibodies, to various carriers, enhancing drug delivery systems.
  • Research in Neuroscience: It plays a role in developing neuropeptides, which are essential for understanding neurological functions and disorders.
  • Cosmetic Formulations: The compound is explored in the cosmetic industry for its potential in formulating products that improve skin health and appearance.

Citations