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Catalog Number:
21034
CAS Number:
467214-46-6
6-Chloro-3-indoxyl-α-D-glucopyranoside
Synonym(s):
6-Chloro-3-(α-D-glucopyranosyloxy)indole, Salmon(tm)-α-D-glucoside
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Product Information

6-Chloro-3-indoxyl-α-D-glucopyranoside is a versatile compound widely utilized in biochemical research and applications. This compound serves as a substrate for various enzymes, particularly in the study of glycosylation processes. Its unique structure allows it to be employed in assays that investigate enzyme activity and substrate specificity, making it invaluable for researchers in enzymology and molecular biology. Additionally, it has applications in the development of biosensors and diagnostic tools, where its reactivity can be harnessed to detect specific biological markers.

The compound's notable features include its stability and solubility, which enhance its usability in laboratory settings. Its ability to undergo hydrolysis under specific conditions allows for the release of indoxyl, a valuable chromogenic agent, facilitating colorimetric detection methods. This makes 6-Chloro-3-indoxyl-α-D-glucopyranoside an essential tool for researchers aiming to explore complex biochemical pathways and develop innovative diagnostic solutions.

Synonyms
6-Chloro-3-(α-D-glucopyranosyloxy)indole, Salmon(tm)-α-D-glucoside
CAS Number
467214-46-6
Molecular Formula
C14H16ClNO6
Molecular Weight
329.73
MDL Number
MFCD04972053
PubChem ID
4616636
Conditions
Conserver à 0-8°C
General Information
Synonyms
6-Chloro-3-(α-D-glucopyranosyloxy)indole, Salmon(tm)-α-D-glucoside
CAS Number
467214-46-6
Molecular Formula
C14H16ClNO6
Molecular Weight
329.73
MDL Number
MFCD04972053
PubChem ID
4616636
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-a-D-glucopyranoside is widely utilized in research focused on:

  • Biochemical Assays: This compound serves as a substrate in enzyme assays, particularly for studying glycosidase activity, allowing researchers to measure enzyme kinetics effectively.
  • Plant Biotechnology: It is used in plant tissue culture as a marker for gene expression, helping scientists track the success of genetic modifications in crops.
  • Diagnostic Applications: The compound can be employed in diagnostic tests to detect specific enzymes related to certain diseases, providing a valuable tool in clinical settings.
  • Pharmaceutical Research: It plays a role in drug development, particularly in the synthesis of indole derivatives, which are important in creating new therapeutic agents.
  • Food Industry: This chemical is utilized in food testing to detect specific glycosidic compounds, ensuring quality control and safety in food products.

Citations