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Catalog Number:
20990
CAS Number:
133950-69-3
5-Bromo-3-indoxyl caprylate
Synonym(s):
5-Bromo-3-indolyl caprylate, 5-Bromo-3-indoxyl octanoate
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Product Information

5-Bromo-3-indoxyl caprylate is a versatile compound recognized for its significant applications in biochemical research and diagnostics. This compound serves as a substrate in enzyme assays, particularly for the detection of β-galactosidase activity, making it invaluable in molecular biology and microbiology laboratories. Its unique structure allows for the generation of a colored product upon enzymatic cleavage, facilitating easy visualization and quantification. Additionally, its lipophilic nature enhances its utility in various formulations, including drug delivery systems and bioassays, where solubility and stability are crucial.

Researchers and industry professionals will appreciate the compound's ability to provide clear results in enzyme activity studies, as well as its potential in developing novel diagnostic tools. Its compatibility with various biological systems and ease of use make it an essential reagent for those exploring enzymatic processes and their applications in health and disease. With its reliable performance and broad applicability, 5-Bromo-3-indoxyl caprylate stands out as a key component in advancing scientific research.

Synonyms
5-Bromo-3-indolyl caprylate, 5-Bromo-3-indoxyl octanoate
CAS Number
133950-69-3
Molecular Formula
C16H20BrNO2
Molecular Weight
338.24
MDL Number
MFCD02683904
PubChem ID
14821426
Conditions
Store at 0-8°C
General Information
Synonyms
5-Bromo-3-indolyl caprylate, 5-Bromo-3-indoxyl octanoate
CAS Number
133950-69-3
Molecular Formula
C16H20BrNO2
Molecular Weight
338.24
MDL Number
MFCD02683904
PubChem ID
14821426
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-3-indoxyl caprylate is widely utilized in research focused on:

  • Biochemical Assays: This compound serves as a substrate in enzyme assays, particularly for detecting β-galactosidase activity, which is crucial in molecular biology and genetic studies.
  • Histochemical Staining: It is used in histochemistry for visualizing specific cellular components, aiding researchers in understanding tissue structure and function.
  • Drug Development: The compound plays a role in the pharmaceutical industry, particularly in developing new therapeutic agents by acting as a model for drug metabolism studies.
  • Fluorescent Probes: It can be utilized in the creation of fluorescent probes for imaging applications in live-cell microscopy, enhancing the visualization of cellular processes.
  • Environmental Monitoring: This chemical is applied in assessing environmental samples for microbial activity, helping in the evaluation of soil and water quality.

Citations