5-Bromo-4-chloro-3-indolyl-beta-D-galactoside

5-Bromo-4-chloro-3-indolyl-beta-D-galactoside Basic information
Product Name:5-Bromo-4-chloro-3-indolyl-beta-D-galactoside
Synonyms:X-BETA-D-GAL;X-BETA-D-GALACTOSIDE;X-BETA-GAL;X-GAL READY TO USE;X-GAL;5-BROMO-4-CHLORO-1H-INDOL-3-YL BETA-D-GALACTOPYRANOSIDE;5-BROMO-4-CHLORO-1H-INDOL-3-YL BETA-D-GALACTOSIDE-(1,5);5-BROMO-4-CHLORO-3-INDOLYL-B B-D-GALACTOPYRANOSIDE
CAS:7240-90-6
MF:C14H15BrClNO6
MW:408.63
EINECS:230-640-8
Product Categories:Fluorescent Labels & Indicators;Labeling and Diagnostics Reagents;substrate;Carbohydrates & Derivatives;Enzyme substrates
Mol File:7240-90-6.mol
5-Bromo-4-chloro-3-indolyl-beta-D-galactoside Structure
5-Bromo-4-chloro-3-indolyl-beta-D-galactoside Chemical Properties
Melting point 230 °C
alpha -64 º (C=1, H2O/DMF (1/1))
Boiling point 673.9±55.0 °C(Predicted)
density 1.5563 (rough estimate)
refractive index 1.6110 (estimate)
storage temp. -20°C
solubility Soluble in 100 mM in DMSO.
pka12.74±0.70(Predicted)
form Powder
color White
OdorOdorless
Sensitive Moisture & Light Sensitive
Merck 14,10074
BRN 1402009
Stability:Stable. Incompatible with strong oxidizing agents.
InChIKeyOPIFSICVWOWJMJ-AEOCFKNESA-N
CAS DataBase Reference7240-90-6(CAS DataBase Reference)
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 24/25-37/39-26
WGK Germany 3
8-10-21
HazardClass IRRITANT
HS Code 29389090
MSDS Information
ProviderLanguage
ACROSEnglish
SigmaAldrichEnglish
ALFAEnglish
5-Bromo-4-chloro-3-indolyl-beta-D-galactoside Usage And Synthesis
Chemical PropertiesWhite Powder
UsesA substrate for -Galactosidase that is converted by the enzyme into an intense indigo-blue chromophore (615 nm)
UsesIn histochemical staining, in blue-white selection of bacterial colonies with lacZ gene activity during cloning experiments.
Usesmagenta b-galactosidase substrate
UsesA substrate for β-Galactosidase that is converted by the enzyme into an intense indigo-blue chromophore (615 nm).
DefinitionChEBI: An indolyl carbohydrate that is the beta-D-galactoside of 3-hydroxy-1H-indole in which the indole moiety is substituted at positions 4 and 5 by chlorine and bromine, respectively. It is used to test for he presence of an enzyme, beta-galactosidase, which cleaved the glycosidic bond to give 5-bromo-4-chloro-3-hydroxy-1H-indole, which immediately dimerises to give an intensely blue product.
5-Bromo-4-chloro-3-indolyl-beta-D-galactoside Preparation Products And Raw materials

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