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Catalog Number:
21388
CAS Number:
93863-89-9
5-Bromo-6-chloro-3-indoxyl-β-D-glucopyranoside
Purity:
≥ 99% (TLC)
Synonym(s):
5-Bromo-6-chloro-3-indolyl β-d-glucopyranoside
Documents
$51.18 /250MG
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Product Information

5-Bromo-6-chloro-3-indoxyl-β-D-glucopyranoside is a versatile compound widely utilized in biochemical research and applications. This compound serves as a chromogenic substrate for the detection of β-galactosidase, making it invaluable in molecular biology and genetic studies. Its unique structure allows for the visualization of enzyme activity, facilitating the study of gene expression and enzyme function in various biological systems. Researchers appreciate its ability to produce a distinct color change upon enzymatic reaction, which aids in quantifying enzyme activity with precision.

In addition to its applications in research, 5-Bromo-6-chloro-3-indoxyl-β-D-glucopyranoside is also employed in the development of diagnostic assays and biosensors. Its stability and reactivity make it an excellent choice for creating sensitive detection methods in clinical and environmental settings. The compound's compatibility with various analytical techniques further enhances its utility, making it a preferred choice for professionals in the fields of biochemistry and molecular biology.

Synonyms
5-Bromo-6-chloro-3-indolyl β-d-glucopyranoside
CAS Number
93863-89-9
Purity
≥ 99% (TLC)
Molecular Formula
C14H15BrClNO6
Molecular Weight
408.63
MDL Number
MFCD00210022
PubChem ID
4131401
Appearance
White powder
Optical Rotation
[a]D20 = -52 ± 2º (C=1 in DMF:H2O=1:1)
Conditions
Store at 0-8 °C
General Information
Synonyms
5-Bromo-6-chloro-3-indolyl β-d-glucopyranoside
CAS Number
93863-89-9
Purity
≥ 99% (TLC)
Molecular Formula
C14H15BrClNO6
Molecular Weight
408.63
MDL Number
MFCD00210022
PubChem ID
4131401
Appearance
White powder
Optical Rotation
[a]D20 = -52 ± 2º (C=1 in DMF:H2O=1:1)
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-6-chloro-3-indoxyl-b-D-glucopyranoside is widely utilized in research focused on:

  • Biochemical Assays: This compound serves as a substrate in enzyme assays, particularly for detecting β-glucosidase activity, which is crucial in various biochemical research applications.
  • Histochemical Staining: It is employed in histochemistry for visualizing specific enzyme activities in tissue samples, aiding in the study of cellular processes and disease mechanisms.
  • Plant Research: Used in plant biology, it helps in studying gene expression related to glucoside metabolism, providing insights into plant physiology and development.
  • Pharmaceutical Development: This compound can be a part of drug formulation research, particularly in developing targeted therapies that utilize enzyme interactions for improved efficacy.
  • Biotechnology Applications: It is valuable in genetic engineering, where it can be used to track the expression of transgenes in modified organisms, enhancing the understanding of genetic modifications.

Citations