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Catalog Number:
21307
CAS Number:
207606-55-1
5-Bromo-4-chloro-3-indoxyl-β-D-xylopyranoside
Synonym(s):
5-Bromo-4-chloro-3-indolyl β-D-xylopyranoside
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Product Information

5-Bromo-4-chloro-3-indoxyl-β-D-xylopyranoside is a versatile compound widely utilized in biochemical research and applications. This compound serves as a substrate for various enzymatic reactions, particularly in the study of glycosyltransferases and other carbohydrate-active enzymes. Its unique structure, featuring both bromine and chlorine substituents, enhances its reactivity and makes it an excellent choice for probing enzyme specificity and activity in glycosylation processes. Researchers often employ this compound in assays to visualize enzyme activity, providing a clear and effective means of studying carbohydrate metabolism.

In addition to its applications in enzymology, 5-Bromo-4-chloro-3-indoxyl-β-D-xylopyranoside is also valuable in the field of plant biotechnology. It can be used as a marker in transgenic plants, allowing for the identification of successful gene integration and expression. This compound's ability to produce a colorimetric response upon enzymatic cleavage makes it an essential tool for researchers aiming to enhance crop traits through genetic modification. Its practicality and effectiveness in various applications make it a preferred choice for professionals in both academic and industrial settings.

Synonyms
5-Bromo-4-chloro-3-indolyl β-D-xylopyranoside
CAS Number
207606-55-1
Molecular Formula
C13H13BrClNO5
Molecular Weight
378.61
MDL Number
MFCD00152013
PubChem ID
42609173
Conditions
Store at 0-8°C
General Information
Synonyms
5-Bromo-4-chloro-3-indolyl β-D-xylopyranoside
CAS Number
207606-55-1
Molecular Formula
C13H13BrClNO5
Molecular Weight
378.61
MDL Number
MFCD00152013
PubChem ID
42609173
Conditions
Store at 0-8°C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

5-Bromo-4-chloro-3-indoxyl-b-D-xylopyranoside is widely utilized in research focused on:

  • Enzyme Substrates: This compound serves as a substrate for various enzymes, particularly in the study of glycosylation processes, aiding researchers in understanding enzyme specificity and activity.
  • Histochemical Staining: It is used in histochemistry for visualizing enzyme activity in tissue samples, providing a clear indication of biological processes in medical research.
  • Biotechnology Applications: In genetic engineering, it helps in the identification of transformed cells, allowing for efficient selection in plant and microbial studies.
  • Pharmaceutical Research: The compound is explored for its potential in drug development, particularly in targeting specific biological pathways, enhancing therapeutic efficacy.
  • Analytical Chemistry: It is utilized in assays and analytical methods to quantify enzyme activity, offering precise measurements that are crucial for various biochemical studies.

Citations