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Catalog Number:
21204
CAS Number:
33993-25-8
2-Naphthyl-β-D-galactopyranoside
Synonym(s):
2-Naphthalenyl-β-D-glucopyranoside, β-Naphthyl-β-D-galactopyranoside
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Product Information

2-Naphthyl-b-D-galactopyranoside is a versatile glycoside that plays a crucial role in biochemical research and applications. This compound is recognized for its ability to serve as a substrate in enzyme assays, particularly for β-galactosidase, making it invaluable in the study of enzyme kinetics and metabolic pathways. Its unique structure, featuring a naphthyl group, enhances its solubility and reactivity, allowing for efficient interaction with biological systems. Researchers utilize this compound in various applications, including the development of biosensors and the study of carbohydrate metabolism, providing insights into cellular processes and disease mechanisms.

In addition to its research applications, 2-Naphthyl-b-D-galactopyranoside is also employed in the synthesis of complex carbohydrates and as a tool for studying glycosylation processes. Its ability to mimic natural substrates makes it an excellent choice for exploring the roles of glycosides in biological systems. With its broad range of applications and significant relevance in both academic and industrial settings, this compound stands out as a key reagent for professionals in biochemistry and molecular biology.

Synonyms
2-Naphthalenyl-β-D-glucopyranoside, β-Naphthyl-β-D-galactopyranoside
CAS Number
33993-25-8
Molecular Formula
C16H18O6
Molecular Weight
306.31
MDL Number
MFCD00004056
PubChem ID
118126
Conditions
Store at 0-8°C
General Information
Synonyms
2-Naphthalenyl-β-D-glucopyranoside, β-Naphthyl-β-D-galactopyranoside
CAS Number
33993-25-8
Molecular Formula
C16H18O6
Molecular Weight
306.31
MDL Number
MFCD00004056
PubChem ID
118126
Conditions
Store at 0-8°C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

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

  • Enzyme Substrates: This compound serves as a substrate for various glycosidases, allowing researchers to study enzyme activity and kinetics in carbohydrate metabolism.
  • Cell Biology: It is used in cell culture studies to investigate the uptake and metabolism of carbohydrates, providing insights into cellular processes and signaling pathways.
  • Fluorescent Probes: The compound can be modified to create fluorescent probes, which are valuable in imaging techniques for tracking biological molecules in live cells.
  • Drug Development: It plays a role in the design of glycosylated drugs, enhancing their bioavailability and specificity, which is crucial in pharmaceutical research.
  • Food Industry: This chemical is also explored for its potential applications in food science, particularly in understanding sugar interactions and flavor development.

Citations