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Catalog Number:
21019
CAS Number:
36473-36-6
5-Iodo-3-indoxyl-β-D-galactopyranoside
Synonym(s):
Iodo-β-D-gal
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Product Information

5-Iodo-3-indoxyl-b-D-galactopyranoside is a valuable compound widely utilized in biochemical research and diagnostics. This synthetic galactoside derivative serves as a chromogenic substrate for the detection of β-galactosidase activity, making it an essential tool in molecular biology and microbiology. When hydrolyzed by β-galactosidase, it produces a colored indigo dye, which allows for easy visualization and quantification of enzyme activity in various biological samples. This property is particularly beneficial in applications such as gene expression studies, enzyme assays, and the identification of genetically modified organisms.

Researchers and industry professionals appreciate the compound's specificity and sensitivity, which enhance the accuracy of experimental results. Its unique structure, featuring an iodine atom, contributes to its stability and reactivity, setting it apart from similar substrates. Moreover, 5-Iodo-3-indoxyl-b-D-galactopyranoside is compatible with a range of biological systems, making it a versatile choice for laboratories focused on enzymology, genetic research, and agricultural biotechnology.

Synonyms
Iodo-β-D-gal
CAS Number
36473-36-6
Molecular Formula
C14H16INO6
Molecular Weight
421.18
MDL Number
MFCD00798400
PubChem ID
3385580
Conditions
Store at 0-8°C
General Information
Synonyms
Iodo-β-D-gal
CAS Number
36473-36-6
Molecular Formula
C14H16INO6
Molecular Weight
421.18
MDL Number
MFCD00798400
PubChem ID
3385580
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-Iodo-3-indoxyl-b-D-galactopyranoside is widely utilized in research focused on:

  • Enzyme Substrate Development: This compound serves as a substrate for various enzymes, particularly in the study of glycosylation processes, allowing researchers to investigate enzyme activity and specificity.
  • Histochemical Staining: It is employed in histochemistry for visualizing enzyme activity in tissue samples, providing a clear indication of the presence of specific enzymes, which is crucial in pathology and biological research.
  • Biochemical Assays: The compound is used in biochemical assays to measure the activity of β-galactosidase, facilitating the study of gene expression and regulation in molecular biology.
  • Drug Development: In pharmaceutical research, it aids in the screening of potential drug candidates that target glycosylation pathways, which are significant in various diseases, including cancer.
  • Diagnostic Applications: This chemical can be utilized in developing diagnostic tools for detecting certain diseases by identifying specific enzyme activities in biological samples, enhancing early diagnosis and treatment strategies.

Citations