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Catalog Number:
21642
CAS Number:
38597-12-5
4-méthylumbelliféryl-α-D-galactopyranoside
Purity:
≥ 98% (HPLC)
Synonym(s):
4-méthylumbelliféryl-α-D-galactoside
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Product Information

4-Methylumbelliferyl-a-D-galactopyranoside is a highly valuable compound widely utilized in biochemical research and enzyme assays. This substrate is particularly effective for detecting and quantifying the activity of galactosidases, making it an essential tool in various fields, including microbiology, molecular biology, and biochemistry. Its unique structure allows for fluorescence upon hydrolysis, enabling researchers to easily monitor enzymatic reactions in real-time.

This compound's practical applications extend to the study of carbohydrate metabolism and the characterization of glycosidases, which are crucial in understanding various biological processes and disease mechanisms. Additionally, its use in high-throughput screening assays can significantly enhance the efficiency of drug discovery and development. With its reliable performance and ease of use, 4-Methylumbelliferyl-a-D-galactopyranoside stands out as a preferred choice for researchers seeking to advance their studies in enzymology and related disciplines.

Synonyms
4-méthylumbelliféryl-α-D-galactoside
CAS Number
38597-12-5
Purity
≥ 98% (HPLC)
Molecular Formula
C16H18O8
Molecular Weight
338.31
MDL Number
MFCD00063278
PubChem ID
119835
Appearance
White powder
Conditions
Conserver à 0-8°C
General Information
Synonyms
4-méthylumbelliféryl-α-D-galactoside
CAS Number
38597-12-5
Purity
≥ 98% (HPLC)
Molecular Formula
C16H18O8
Molecular Weight
338.31
MDL Number
MFCD00063278
PubChem ID
119835
Appearance
White powder
Conditions
Conserver à 0-8°C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

4-Methylumbelliferyl-a-D-galactopyranoside is widely utilized in research focused on:

  • Enzyme Activity Assays: This compound serves as a substrate for various glycosidases, enabling researchers to measure enzyme activity in biochemical assays effectively.
  • Fluorescent Labeling: It can be used in fluorescence microscopy to visualize cellular processes, providing insights into cellular functions and interactions.
  • Microbial Identification: This chemical aids in differentiating bacterial species based on their ability to hydrolyze the compound, which is crucial in microbiology.
  • Food Industry Applications: It is utilized in food testing to detect specific enzymes, ensuring quality control and safety in food products.
  • Pharmaceutical Research: The compound is valuable in drug development studies, particularly in understanding carbohydrate metabolism and its implications in health.

Citations