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Catalog Number:
22048
CAS Number:
3767-28-0
4-Nitrophényl-α-D-glucopyranoside
Purity:
≥ 98 % (HPLC)
Synonym(s):
p -nitrophényl-α-D-glucoside
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Product Information

4-Nitrophenyl-a-D-glucopyranoside is a versatile compound widely utilized in biochemical research and enzymatic assays. This glycoside serves as a substrate for various glycosidases, making it an essential tool for studying enzyme kinetics and mechanisms. Its unique structure, featuring a nitrophenyl group, allows for easy detection and quantification of enzymatic activity, which is crucial in fields such as molecular biology and biochemistry. Researchers often employ this compound in assays to measure the activity of enzymes involved in carbohydrate metabolism, providing insights into metabolic pathways and potential therapeutic targets.

Additionally, 4-Nitrophenyl-a-D-glucopyranoside is beneficial in the development of biosensors and diagnostic tools due to its ability to produce a measurable color change upon enzymatic hydrolysis. This property enhances its applicability in clinical diagnostics and environmental monitoring, where rapid and accurate detection of specific enzymes is required. Its stability and ease of use further contribute to its popularity among researchers and industry professionals seeking reliable reagents for their studies.

Synonyms
p -nitrophényl-α-D-glucoside
CAS Number
3767-28-0
Purity
≥ 98 % (HPLC)
Molecular Formula
C 12 H 15 NON 8
Molecular Weight
301.25
MDL Number
MFCD00064088
PubChem ID
259380
Appearance
Poudre cristalline blanc cassé
Optical Rotation
[a] D 21 = 215 - 218 ° (C = 1 dans H 2 O)
Conditions
Conserver à 0 - 8 °C
General Information
Synonyms
p -nitrophényl-α-D-glucoside
CAS Number
3767-28-0
Purity
≥ 98 % (HPLC)
Molecular Formula
C 12 H 15 NON 8
Molecular Weight
301.25
MDL Number
MFCD00064088
PubChem ID
259380
Appearance
Poudre cristalline blanc cassé
Optical Rotation
[a] D 21 = 215 - 218 ° (C = 1 dans H 2 O)
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-Nitrophenyl-a-D-glucopyranoside 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 kinetics effectively.
  • Biochemical Research: It aids in studying carbohydrate metabolism and enzyme interactions, providing insights into cellular processes and potential therapeutic targets.
  • Drug Development: The compound is used in the development of glycosidase inhibitors, which can lead to new treatments for diseases like diabetes and cancer.
  • Analytical Chemistry: It is employed in chromatographic techniques for the separation and identification of glycosides, enhancing the accuracy of chemical analyses.
  • Food Industry Applications: This chemical can be used to assess the quality of food products by measuring glycosidase activity, ensuring safety and compliance with health standards.

Citations