Weight | 669.967 g/mol |
---|---|
Formula | C19H10Br4O5S |
Hydrogen Acceptors | 5 |
Hydrogen Donors | 2 |
Aromatic Rings | 3 |
Rotatable Bonds | 2 |
Bromophenol blue (115-39-9)
Bromphenol Blue · Tetrabromophenol Blue
Score:
#983 in Biochemistry
,
#1134 in Physics
,
#3229 in Chemistry
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- THE CYTOCHEMICAL STAINING AND MEASUREMENT OF PROTEIN WITH MERCURIC BROMPHENOL BLUE (The Biological Bulletin, 1953)
- A rapid and reproducible assay for quantitative estimation of proteins using bromophenol blue. (Analytical Biochemistry, 1978)
- Penetration of bromophenol blue from the perfused cerebral ventricles into the brain tissue (The Journal of Physiology, 1960)
- Heterogeneous photodecolorization of mixture of methylene blue and bromophenol blue using CuO-nano-clinoptilolite (Journal of Industrial and Engineering Chemistry, 2014)
- Microdetermination of Proteins by Resonance Light Scattering Spectroscopy with Bromophenol Blue (Analytical Biochemistry, 1996)
- Kinetics of the oxidative color removal and degradation of bromophenol blue with hydrogen peroxide catalyzed by copper(II)-supported alumina and zirconia (Applied Catalysis B-environmental, 2000)
-
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - Bromphenol Blue
- Tetrabromophenol Blue
-
SMILESC1=CC=C2C(=C1)C(OS2(=O)=O)(C3=CC(=C(C(=C3)Br)O)Br)C4=CC(=C(C(=C4)Br)O)Br
-
InChIKeyUDSAIICHUKSCKT-UHFFFAOYSA-N
- Pubchem - Bromophenol blue
- Wikipedia - bromophenol blue
Bromophenol blue (3,3,5,5-tetrabromophenolsulfonphthalein, BPB, albutest) is used as a pH indicator, a color marker, and a dye. It can be prepared by slowly adding excess bromine to a hot solution of phenolsulfonphthalein in glacial acetic acid.
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Synthesis
2,6-DIBROMOPHENOL
+
Reactant
(Friedel-Crafts alkylation)
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