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

Names

[ Name ]:
5-Bromo-4-chloro-3-indolyl-beta-D-glucoside

[Synonym ]:
MFCD00063690
5-Bromo-4-chloro-3-indolyl-β-D-glucoside
β-D-Glucopyranose, 2-O-(5-bromo-4-chloro-1H-indol-3-yl)-, ion(1-)
5-bromo-4-chloro-3-indolyl beta-D-glucoside
(2R,3R,4S,5S,6R)-3-[(5-Bromo-4-chloro-1H-indol-3-yl)oxy]-4,5-dihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-olate
X-Glc X-glucoside
EINECS 239-603-0

Biological Activity

[Description]:

5-Bromo-4-chloro-3-indolyl β-D-Glucopyranoside is a biochemical reagent that can be used as a biological material or organic compound for life science related research.

[Related Catalog]:

Research Areas >> Others

Chemical & Physical Properties

[ Density]:
1.882 g/cm3

[ Boiling Point ]:
698.0±55.0 °C at 760 mmHg

[ Melting Point ]:
249-251ºC

[ Molecular Formula ]:
C₁₄H₁₅BrClNO₆

[ Molecular Weight ]:
407.622

[ Flash Point ]:
375.9±31.5 °C

[ Exact Mass ]:
405.969849

[ PSA ]:
115.17000

[ LogP ]:
1.50

[ Vapour Pressure ]:
0.0±2.3 mmHg at 25°C

[ Index of Refraction ]:
1.731

MSDS

Click to get detail MSDS

Safety Information

[ Personal Protective Equipment ]:
Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter

[ Hazard Codes ]:
Xi

[ Safety Phrases ]:
S24/25

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

[ HS Code ]:
29389090

Articles

SUBSTRATES FOR CYTOCHEMICAL DEMONSTRATION OF ENZYME ACTIVITY. I. SOME SUBSTITUTED 3-INDOLYL-BETA-D-GLYCOPYRANOSIDES.

J. Med. Chem. 7 , 574, (1964)

Novel compound for identifying Escherichia coli.

Appl. Environ. Microbiol. 54(7) , 1874-5, (1988)

A new chromogenic compound, 5-bromo-4-chloro-3-indoxyl-beta-D-glucuronide, was found to be useful for the rapid, specific, differential identification of Escherichia coli in the sanitary analysis of s...

Chemiluminescent assay of various enzymes using indoxyl derivatives as substrate and its applications to enzyme immunoassay and DNA probe assay.

Anal. Biochem. 199(2) , 238-42, (1991)

Chemiluminescent assays of various enzymes have been developed using indoxyl derivatives as substrates. The principle of the method is as follows: an enzyme causes hydrolysis of an indoxyl derivative ...