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Catalog Number:
21531
CAS Number:
138182-21-5
6-Chloro-3-indolyl-β-D-galactopyranoside
Purity:
≥ 98% (HPLC)
Synonym(s):
6-Chloro-3-(β-D-galactopyranosyloxy)indole
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Product Information

6-Chloro-3-indolyl-β-D-galactopyranoside is a versatile chemical compound widely recognized for its applications in biochemical research and pharmaceutical development. This compound serves as a substrate for β-galactosidase, making it an essential tool in molecular biology for gene expression studies and enzyme activity assays. Its unique structure, featuring a chloroindole moiety, enhances its reactivity and specificity, allowing researchers to effectively monitor enzymatic processes.

In addition to its role in research, 6-Chloro-3-indolyl-β-D-galactopyranoside has potential applications in the development of therapeutic agents, particularly in the study of glycosylation processes and their implications in disease mechanisms. Its ability to facilitate the detection of β-galactosidase activity makes it invaluable in various diagnostic applications, providing insights into cellular functions and metabolic pathways. Researchers and industry professionals can leverage this compound to advance their studies in enzymology, molecular biology, and drug discovery.

Synonyms
6-Chloro-3-(β-D-galactopyranosyloxy)indole
CAS Number
138182-21-5
Purity
≥ 98% (HPLC)
Molecular Formula
C14H16ClNO6
Molecular Weight
329.73
MDL Number
MFCD01310928
PubChem ID
4616636
Appearance
White to off-white cream powder
Optical Rotation
[a]D20 = -40 - 50 º (C=1 in MeOH)
Conditions
Store at 0 - 8 °C
General Information
Synonyms
6-Chloro-3-(β-D-galactopyranosyloxy)indole
CAS Number
138182-21-5
Purity
≥ 98% (HPLC)
Molecular Formula
C14H16ClNO6
Molecular Weight
329.73
MDL Number
MFCD01310928
PubChem ID
4616636
Appearance
White to off-white cream powder
Optical Rotation
[a]D20 = -40 - 50 º (C=1 in MeOH)
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-indolyl-b-D-galactopyranoside is widely utilized in research focused on:

  • Biochemical Assays: This compound serves as a substrate in enzyme assays, particularly for β-galactosidase, allowing researchers to measure enzyme activity in various biological samples.
  • Cellular Studies: It is used in cell culture experiments to study gene expression and cellular responses, helping scientists understand cellular mechanisms and pathways.
  • Drug Development: The compound plays a role in the development of new pharmaceuticals, particularly in targeting specific enzymes, which can lead to more effective treatments with fewer side effects.
  • Diagnostics: It is utilized in diagnostic tests to detect enzyme deficiencies or abnormalities in metabolic pathways, aiding in the early diagnosis of certain diseases.
  • Research on Glycosylation: This chemical is valuable in studies examining glycosylation processes, which are critical for understanding protein function and interactions in various biological systems.

Citations