📦 Same-day shipping on in-stock items | ⏱️ 99.6% On-time delivery | 🌟 99% Happy customers

Catalog Number:
20984
CAS Number:
6892-58-6
4-Nitrophenyl-α-L-arabinofuranoside
Synonym(s):
p-Nitrophenyl α-L-arabinofuranoside, pNP-α-L-Ara
Documents
Available - Request Bulk Quote
Pack Size Availability Price
Request Bulk Quote
Product Information

4-Nitrophenyl-a-L-arabinofuranoside is a versatile glycoside that plays a significant role in biochemical research and applications. This compound is recognized for its utility in enzymatic assays, particularly in the study of glycosidases, where it serves as a substrate to investigate enzyme kinetics and mechanisms. Its unique structure, featuring a nitrophenyl group, enhances its reactivity and makes it an excellent choice for probing carbohydrate-active enzymes. Researchers often utilize this compound in the synthesis of more complex carbohydrates, facilitating advancements in glycoscience and related fields.

In addition to its applications in enzymology, 4-Nitrophenyl-a-L-arabinofuranoside is also valuable in the development of diagnostic tools and therapeutic agents. Its ability to release nitrophenol upon hydrolysis allows for easy monitoring of enzymatic activity, making it a preferred choice for laboratories focused on carbohydrate metabolism studies. The compound's stability and solubility in aqueous solutions further enhance its practicality in various experimental setups, ensuring reliable results in both academic and industrial research environments.

Synonyms
p-Nitrophenyl α-L-arabinofuranoside, pNP-α-L-Ara
CAS Number
6892-58-6
Molecular Formula
C11H13NO7
Molecular Weight
271.22
MDL Number
MFCD00057269
PubChem ID
4374619
Conditions
Store at 0-8°C
General Information
Synonyms
p-Nitrophenyl α-L-arabinofuranoside, pNP-α-L-Ara
CAS Number
6892-58-6
Molecular Formula
C11H13NO7
Molecular Weight
271.22
MDL Number
MFCD00057269
PubChem ID
4374619
Conditions
Store at 0-8°C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

4-Nitrophenyl-a-L-arabinofuranoside is widely utilized in research focused on:

  • Glycosylation Studies: This compound serves as a glycosyl donor in synthetic chemistry, enabling researchers to create complex carbohydrates for studying biological processes.
  • Enzyme Activity Assays: It is commonly used in assays to evaluate the activity of glycosidases, helping scientists understand enzyme kinetics and mechanisms.
  • Drug Development: The compound plays a role in the development of glycosylated drugs, which can enhance bioavailability and efficacy compared to non-glycosylated counterparts.
  • Biochemical Research: It aids in the investigation of carbohydrate-binding proteins, contributing to the understanding of cell signaling and recognition processes.
  • Analytical Chemistry: The compound is utilized in various analytical techniques, such as chromatography, to separate and identify carbohydrate structures in complex mixtures.

Citations