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Catalog Number:
49290
CAS Number:
7699-38-9
4-Nitrophényl N , N ', N ''-triacétyl-b-chitotrioside
Purity:
≥ 98 % (HPLC)
Synonym(s):
GlcNAcb(1-4)GlcNAcb(1-4)GlcNAc-b- p NP, 4-nitrophényl2-acétamido-2-désoxy-bD-glucopyranosyl-(1→4)-2-acétamido-2-désoxy-bD-glucopyranosyl-(1→4)-2-acétamido-2-désoxy-bD-glucopyranoside
Documents
$464.60 /5 mg
Taille
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Informations sur le produit

4-Nitrophenyl N,N',N''-triacetyl-b-chitotrioside is a specialized glycoside compound that has garnered attention in various fields, particularly in biochemistry and pharmaceuticals. This compound is recognized for its unique structural features, which enhance its solubility and reactivity, making it an ideal candidate for use in enzyme assays and as a substrate in glycosylation reactions. Researchers often utilize this compound to study enzyme kinetics and mechanisms, as it serves as an effective model for understanding glycosylation processes in biological systems.

Additionally, its potential applications extend to drug development, where it can be employed in the synthesis of glycosylated compounds that exhibit improved pharmacological properties. The presence of the nitrophenyl group not only aids in detection but also enhances the compound's reactivity, making it a valuable tool in synthetic organic chemistry. With its diverse applications and significant advantages over similar compounds, 4-Nitrophenyl N,N',N''-triacetyl-b-chitotrioside is an essential resource for researchers and industry professionals looking to innovate in their respective fields.

Numéro CAS 
7699-38-9
Formule moléculaire
C 30 H 44 N 4 O 18
Poids moléculaire 
748.69
Point de fusion 
239 - 241 °C
Informations générales
Numéro CAS 
7699-38-9
Formule moléculaire
C 30 H 44 N 4 O 18
Poids moléculaire 
748.69
Point de fusion 
239 - 241 °C
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

4-Nitrophenyl N,N',N''-triacetyl-b-chitotrioside is widely utilized in research focused on:

  • Biotechnology: This compound serves as a substrate in enzymatic assays, particularly for studying chitinase activity, which is crucial in understanding insect physiology and plant-pathogen interactions.
  • Drug Development: It plays a role in the synthesis of glycosylated compounds, aiding in the creation of new pharmaceuticals that target specific biological pathways, enhancing drug efficacy.
  • Diagnostics: The compound is used in the development of diagnostic kits for detecting chitinase levels in various biological samples, which can indicate certain diseases or conditions.
  • Material Science: It is incorporated into biocompatible materials for tissue engineering applications, providing a scaffold that promotes cell adhesion and growth.
  • Agricultural Research: This chemical is utilized in studies aimed at improving pest resistance in crops by understanding the role of chitinases in plant defense mechanisms.

Citations