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Catalog Number:
00238
CAS Number:
369-07-3
2-Nitrophényl-β-D-galactopyranoside
Purity:
≥ 99 % (HPLC)
Synonym(s):
2-Nitrophényl-β-D-galactoside
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Informations sur le produit

2-Nitrophenyl-b-D-galactopyranoside is a valuable compound widely utilized in biochemical research and enzymatic studies. This substrate is particularly important for the detection and quantification of β-galactosidase activity, making it an essential tool in molecular biology and biochemistry laboratories. Its unique structure allows for the release of a colored product upon enzymatic hydrolysis, facilitating easy monitoring of enzyme activity. Researchers often employ this compound in assays to study enzyme kinetics, gene expression, and metabolic pathways, providing insights into cellular processes and disease mechanisms.

Additionally, 2-Nitrophenyl-b-D-galactopyranoside is recognized for its stability and solubility in various solvents, which enhances its applicability in diverse experimental setups. Its use extends to the development of biosensors and diagnostic kits, where precise measurement of enzyme activity is crucial. By choosing this compound, researchers can achieve reliable results, contributing to advancements in biotechnology and pharmaceutical development.

Numéro CAS 
369-07-3
Formule moléculaire
C 12 H 15 NON 8
Poids moléculaire 
301.3
Point de fusion 
195 °C (déc.)
Rotation optique 
[a] D 20 = -67 à -73 º (C=1 dans H 2 O)
Informations générales
Numéro CAS 
369-07-3
Formule moléculaire
C 12 H 15 NON 8
Poids moléculaire 
301.3
Point de fusion 
195 °C (déc.)
Rotation optique 
[a] D 20 = -67 à -73 º (C=1 dans H 2 O)
Propriétés
Informations complémentaires sur la propriété à venir prochainement !
-
Sécurité et réglementation
Matières dangereuses
-
Antibiotique
-
Réglementé par la DEA
Non
Avertissements 
-
Applications

2-Nitrophenyl-b-D-galactopyranoside is widely utilized in research focused on:

  • Enzyme Activity Assays: This compound serves as a substrate for various glycosidases, allowing researchers to measure enzyme activity and understand their kinetics in biochemical studies.
  • Cellular Uptake Studies: It can be used to investigate the mechanisms of sugar transport in cells, providing insights into cellular metabolism and potential therapeutic targets.
  • Fluorescent Probes: When coupled with fluorescent tags, it can be employed in imaging studies to visualize cellular processes, enhancing the understanding of cellular dynamics.
  • Drug Development: The compound's ability to mimic natural substrates makes it valuable in the design of new drugs targeting glycosidases, contributing to advancements in pharmaceutical research.
  • Biochemical Pathway Analysis: It aids in the elucidation of metabolic pathways involving carbohydrates, helping researchers to map out complex biological processes.

Citations