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Catalog Number:
21383
CAS Number:
133950-77-3
Nonanoate de 5-bromo-4-chloro-3-indoxyle
Synonym(s):
Nonanoate de 5-bromo-4-chloro-3-indolyle
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Product Information

5-Bromo-4-chloro-3-indoxyl nonanoate is a versatile chemical compound widely utilized in biochemical research and applications. This compound serves as a substrate for various enzymatic reactions, particularly in the field of molecular biology, where it is employed in the detection of specific enzymes through colorimetric assays. Its unique structure allows for selective interactions, making it an ideal choice for researchers looking to study enzyme activity and metabolic pathways. Additionally, its stability and solubility in organic solvents enhance its usability in laboratory settings, facilitating a range of experimental designs.

In practical applications, 5-Bromo-4-chloro-3-indoxyl nonanoate is particularly valuable in histochemical staining techniques, where it aids in visualizing enzyme localization within tissues. This capability is crucial for studies in pathology and developmental biology, providing insights into cellular processes and disease mechanisms. Researchers benefit from its reliable performance and the clarity of results it delivers, making it a preferred choice for those seeking to advance their studies in enzymology and related fields.

Synonyms
Nonanoate de 5-bromo-4-chloro-3-indolyle
CAS Number
133950-77-3
Molecular Formula
C 17 H 21 BrClNO 2
Molecular Weight
386.72
MDL Number
MFCD02683900
PubChem ID
14821433
Conditions
Conserver à 0-8°C
General Information
Synonyms
Nonanoate de 5-bromo-4-chloro-3-indolyle
CAS Number
133950-77-3
Molecular Formula
C 17 H 21 BrClNO 2
Molecular Weight
386.72
MDL Number
MFCD02683900
PubChem ID
14821433
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

5-Bromo-4-chloro-3-indoxyl nonanoate is widely utilized in research focused on:

  • Biotechnology: This compound serves as a substrate for enzyme assays, particularly in the detection of β-galactosidase activity, which is crucial for genetic studies and recombinant DNA technology.
  • Histochemistry: It is employed as a chromogenic substrate in histochemical staining techniques, allowing researchers to visualize enzyme activity in tissue samples, enhancing the understanding of cellular processes.
  • Pharmaceutical Development: The compound is used in drug formulation research, particularly in developing targeted delivery systems due to its unique chemical properties that can improve bioavailability.
  • Environmental Monitoring: It can be utilized in assays to detect specific microbial activities in environmental samples, aiding in pollution assessment and bioremediation efforts.
  • Food Safety Testing: This chemical is applied in testing for microbial contamination in food products, ensuring safety and compliance with health regulations.

Citations