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Catalog Number:
21620
CAS Number:
2816-24-2
2-Nitrofenil-β-D-glucopiranósido
Purity:
≥ 99 % (HPLC)
Synonym(s):
2-Nitrofenil-β-D-glucósido
Documents
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Tamaño
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Product Information

2-Nitrophenyl-b-D-glucopyranoside is a versatile compound widely utilized in biochemical research and pharmaceutical applications. This glycoside derivative features a nitrophenyl group, which enhances its reactivity and makes it an excellent substrate for various enzymatic reactions, particularly in the study of glycosidases. Its unique structure allows researchers to explore carbohydrate metabolism and enzyme kinetics effectively, providing insights into biological processes.

In addition to its research applications, 2-Nitrophenyl-b-D-glucopyranoside serves as a valuable tool in the development of glycosylation reactions and can be employed in the synthesis of more complex carbohydrate structures. Its ability to act as a chromogenic substrate enables easy monitoring of enzymatic activity, making it a preferred choice for laboratories focused on enzyme characterization and assay development. The compound's stability and solubility in aqueous solutions further enhance its usability in various experimental setups, ensuring reliable results.

Synonyms
2-Nitrofenil-β-D-glucósido
CAS Number
2816-24-2
Purity
≥ 99 % (HPLC)
Molecular Formula
C12H15Nº8
Molecular Weight
301.25
MDL Number
MFCD00065048
PubChem ID
219973
Appearance
Polvo de color blanquecino a amarillo pálido
Conditions
Conservar entre 0 y 8°C
General Information
Synonyms
2-Nitrofenil-β-D-glucósido
CAS Number
2816-24-2
Purity
≥ 99 % (HPLC)
Molecular Formula
C12H15Nº8
Molecular Weight
301.25
MDL Number
MFCD00065048
PubChem ID
219973
Appearance
Polvo de color blanquecino a amarillo pálido
Conditions
Conservar entre 0 y 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-Nitrophenyl-b-D-glucopyranoside is widely utilized in research focused on:

  • Enzyme Assays: This compound serves as a substrate in enzyme assays, particularly for glycosidases. Its use allows researchers to measure enzyme activity effectively, providing insights into enzyme kinetics and mechanisms.
  • Biochemical Research: It is employed in studies related to carbohydrate metabolism and glycosylation processes, helping scientists understand the role of sugars in biological systems.
  • Drug Development: The compound is used in the development of glycosylated drugs, which can enhance the pharmacokinetics and bioavailability of therapeutic agents, making them more effective.
  • Fluorescent Probes: Due to its nitrophenyl group, it can be modified to create fluorescent probes for imaging studies, aiding in cellular and molecular biology research.
  • Food Industry: It finds applications in the food industry for testing the activity of enzymes involved in carbohydrate breakdown, ensuring the quality and safety of food products.

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