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Catalog Number:
21321
CAS Number:
159954-34-4
6-Chloro-3-indoxyl butyrate
Synonym(s):
6-Chloro-3-indolyl butyrate
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Product Information

6-Chloro-3-indoxyl butyrate is a versatile compound widely utilized in biochemical research and various industrial applications. Known for its role as a chromogenic substrate, it is particularly valuable in enzymatic assays, where it serves as a substrate for β-glucuronidase and other enzymes. This compound facilitates the visualization of enzymatic activity through the formation of a colored product, making it an essential tool in histochemistry and molecular biology. Its unique properties allow researchers to easily track and quantify enzyme activity, providing critical insights into metabolic pathways and enzyme kinetics.

In addition to its applications in research, 6-Chloro-3-indoxyl butyrate is also employed in the development of diagnostic tests and assays, enhancing the sensitivity and specificity of detection methods. Its stability and ease of use make it a preferred choice among professionals in laboratories and industrial settings. By incorporating this compound into their workflows, researchers can achieve more accurate results and streamline their processes, ultimately leading to advancements in scientific understanding and innovation.

Synonyms
6-Chloro-3-indolyl butyrate
CAS Number
159954-34-4
Molecular Formula
C12H12ClNO2
Molecular Weight
237.69
MDL Number
MFCD00269775
PubChem ID
2733914
Conditions
Store at 0-8°C
General Information
Synonyms
6-Chloro-3-indolyl butyrate
CAS Number
159954-34-4
Molecular Formula
C12H12ClNO2
Molecular Weight
237.69
MDL Number
MFCD00269775
PubChem ID
2733914
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

6-Chloro-3-indoxyl butyrate is widely utilized in research focused on:

  • Biochemical Assays: This compound serves as a substrate in enzyme assays, particularly for studying β-glucuronidase activity, which is crucial in drug metabolism research.
  • Histochemical Staining: It is employed in histochemistry for visualizing specific cellular components, aiding in the identification of tissue types and disease states.
  • Pharmaceutical Development: Researchers use it to develop and test new drugs, particularly in the field of cancer research, due to its potential to target specific cellular pathways.
  • Plant Biology: This chemical is used in plant research to study gene expression and metabolic pathways, providing insights into plant development and responses to environmental stress.
  • Diagnostic Tools: It has applications in creating diagnostic reagents for detecting certain diseases, enhancing the accuracy of medical tests.

Citations