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Catalog Number:
21409
CAS Number:
425427-87-8
6-Chloro-3-indoxyl-β-D-cellobioside
Synonym(s):
6-Chloro-3-indolyl β-D-cellobiopyranoside
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Product Information

6-Chloro-3-indoxyl-b-D-cellobioside is a versatile compound widely recognized for its applications in biochemical research and plant biology. This compound serves as a substrate for various enzymes, particularly in the study of glycosylation processes. Its unique structure, featuring a chloro-indole moiety, allows it to participate in a range of biochemical reactions, making it an essential tool for researchers investigating enzyme activity and metabolic pathways.

In practical applications, 6-Chloro-3-indoxyl-b-D-cellobioside is utilized in histochemical staining techniques, enabling the visualization of specific enzyme activities in plant tissues. This capability is particularly beneficial for researchers studying plant development and physiology, as it provides insights into the spatial distribution of enzymes. Additionally, its use in molecular biology can aid in the development of biosensors and other diagnostic tools, highlighting its relevance across various scientific fields. With its robust performance and reliability, this compound stands out as a valuable asset for laboratories focused on enzymology and plant sciences.

Synonyms
6-Chloro-3-indolyl β-D-cellobiopyranoside
CAS Number
425427-87-8
Molecular Formula
C20H26ClNO11
Molecular Weight
491.87
MDL Number
MFCD00467205
PubChem ID
53442181
Conditions
Conserver à 0-8°C
General Information
Synonyms
6-Chloro-3-indolyl β-D-cellobiopyranoside
CAS Number
425427-87-8
Molecular Formula
C20H26ClNO11
Molecular Weight
491.87
MDL Number
MFCD00467205
PubChem ID
53442181
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

6-Chloro-3-indoxyl-b-D-cellobioside is widely utilized in research focused on:

  • Plant Biotechnology: This compound serves as a substrate for detecting gene expression in transgenic plants, allowing researchers to visualize the activity of specific genes through colorimetric assays.
  • Enzyme Activity Studies: It acts as a substrate for various glycosyltransferases, helping scientists study enzyme kinetics and mechanisms, which is crucial for understanding metabolic pathways.
  • Pharmaceutical Research: The compound is used in drug development processes, particularly in screening for potential therapeutic agents that target specific biological pathways.
  • Microbial Studies: It aids in identifying and characterizing microbial enzymes, providing insights into microbial metabolism and potential biotechnological applications.
  • Analytical Chemistry: This chemical is utilized in the development of analytical methods for detecting and quantifying glycosylated compounds, enhancing the accuracy of biochemical assays.

Citations