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Catalog Number:
20948
CAS Number:
41335-32-4
1-Naphthyl-β-D-galactopyranoside
Synonym(s):
α-Naphthyl β-D-galactopyranoside, α-Naphthyl-β-D-galactoside
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Product Information

1-Naphthyl-b-D-galactopyranoside is a versatile glycoside that serves as a valuable substrate in various biochemical applications. This compound is particularly recognized for its role in enzyme assays, especially in the study of β-galactosidase activity, making it an essential tool for researchers in enzymology and molecular biology. Its unique structure allows for selective hydrolysis, resulting in the release of 1-naphthol, which can be easily detected and quantified, providing a reliable method for assessing enzyme function.

Additionally, 1-Naphthyl-b-D-galactopyranoside is utilized in the synthesis of glycosylated compounds, contributing to the development of glycoproteins and other biologically relevant molecules. Its application extends to the pharmaceutical industry, where it aids in drug formulation and development processes. The compound's stability and ease of use make it a preferred choice among professionals seeking efficient and effective solutions in their research and industrial applications.

Synonyms
α-Naphthyl β-D-galactopyranoside, α-Naphthyl-β-D-galactoside
CAS Number
41335-32-4
Molecular Formula
C16H18O6
Molecular Weight
306.31
MDL Number
MFCD00067612
PubChem ID
2844794
Conditions
Store at 0-8°C
General Information
Synonyms
α-Naphthyl β-D-galactopyranoside, α-Naphthyl-β-D-galactoside
CAS Number
41335-32-4
Molecular Formula
C16H18O6
Molecular Weight
306.31
MDL Number
MFCD00067612
PubChem ID
2844794
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

1-Naphthyl-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 in biochemical assays. Its specificity helps in understanding enzyme kinetics and mechanisms.
  • 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 Labeling: When conjugated with fluorescent dyes, it can be used for labeling cellular components, enhancing visualization in microscopy and flow cytometry applications.
  • Drug Development: The compound aids in the screening of potential drug candidates that target glycosylation processes, which are crucial in many diseases, including cancer.
  • Food Industry: It can be utilized to assess the activity of enzymes in food products, helping manufacturers optimize processes for better quality and flavor.

Citations