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Catalog Number:
21531
CAS Number:
138182-21-5
6-Cloro-3-indolil-β-D-galactopiranósido
Purity:
≥ 98 % (TLC)
Synonym(s):
6-Cloro-3-(β-D-galactopiranosiloxi)indol
Documents
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Product Information

Es un sustrato de la ?-Galactosidasa y se utiliza como alternativa a X-Gal, para la detección de la actividad enzimática en colonias bacterianas lac+.

Synonyms
6-Cloro-3-(β-D-galactopiranosiloxi)indol
CAS Number
138182-21-5
Purity
≥ 98 % (TLC)
Molecular Formula
C14H16ClNO6
Molecular Weight
329.73
MDL Number
MFCD01310928
PubChem ID
4616636
Appearance
Polvo cremoso de color blanco a blanquecino
Optical Rotation
[a] D 20 = -47 ± 2º (C=1 en MeOH)
Conditions
Conservar entre 0 y 8 °C.
General Information
Synonyms
6-Cloro-3-(β-D-galactopiranosiloxi)indol
CAS Number
138182-21-5
Purity
≥ 98 % (TLC)
Molecular Formula
C14H16ClNO6
Molecular Weight
329.73
MDL Number
MFCD01310928
PubChem ID
4616636
Appearance
Polvo cremoso de color blanco a blanquecino
Optical Rotation
[a] D 20 = -47 ± 2º (C=1 en MeOH)
Conditions
Conservar entre 0 y 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.

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