3D model (Jmol)
|Molar mass||669.96 g·mol−1|
|Melting point||273 °C (523 °F; 546 K)|
|Boiling point||279 °C (534 °F; 552 K)|
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
|what is ?)(|
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.
|Bromophenol blue (pH indicator)|
|below pH 3.0||above pH 4.6|
As an acid–base indicator, its useful range lies between pH 3.0 and 4.6. It changes from yellow at pH 3.0 to blue at pH 4.6; this reaction is reversible. Bromophenol blue is structurally related to phenolphthalein (a popular indicator).
Bromophenol blue is also used as a color marker to monitor the process of agarose gel electrophoresis and polyacrylamide gel electrophoresis. Since bromophenol blue carries a slight negative charge at moderate pH, it will migrate in the same direction as DNA or protein in a gel; the rate at which it migrates varies according to gel density and buffer composition, but in a typical 1% agarose gel in a 1X TAE buffer or TBE buffer, bromophenol blue migrates at the same rate as a DNA fragment of about 300 base pairs, in 2% agarose as 150 bp. Xylene cyanol and orange G may also be used for this purpose.
Bromophenol blue is also used as a dye. At neutral pH, the dye absorbs red light most strongly and transmits blue light. Solutions of the dye, therefore, are blue. At low pH, the dye absorbs ultraviolet and blue light most strongly and appears yellow in solution. In solution at pH 3.6 (in the middle of the transition range of this pH indicator) obtained by dissolution in water without any pH adjustment, bromophenol blue has a characteristic green red color, where the apparent color shifts depending on the concentration and/or path length through which the solution is observed. This phenomenon is called dichromatic color. Bromophenol blue is the substance with the highest known value of Kreft's dichromaticity index. This means it has the largest change in color hue, when the thickness or concentration of observed sample increases or decreases.
- Bromophenol blue at OpenWetWare
- Santa Cruz Biotechnology, Inc. Bromophenol Blue (CAS 115-39-9) Properties. https://www.scbt.com/scbt/product/bromophenol-blue-115-39-9
- Reaxys. Bromophenol blue (115-39-9) Chemical Names and Synonyms.
- PubChem Compound. Bromphenol Blue - Compound Summary. http://pubchem.ncbi.nlm.nih.gov/summary/summary.cgi?cid=8272&loc=ec_rcs
- PubChem Compound. Bromphenol Blue - Use and Manufacturing. http://pubchem.ncbi.nlm.nih.gov/summary/summary.cgi?cid=8272&loc=ec_rcs
- "Agarose gel electrophoresis (basic method)". Retrieved 2008-04-07.
- Kreft S, Kreft M (2007). "Physicochemical and physiological basis of dichromatic colour". Naturwissenschaften. 94 (11): 935–9. Bibcode:2007NW.....94..935K. doi:10.1007/s00114-007-0272-9. PMID 17534588.
- Kreft S, Kreft M. (2009). "Quantification of dichromatism: a characteristic of color in transparent materials". Journal of the Optical Society of America A. 26 (7): 1576–1581. Bibcode:2009JOSAA..26.1576K. doi:10.1364/JOSAA.26.001576. PMID 19568292.