86778
3′,3″,5′,5″-Tetrabromophenolphthalein ethyl ester
suitable for microscopy
Synonym(s):
TBPE
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About This Item
Empirical Formula (Hill Notation):
C22H14Br4O4
CAS Number:
Molecular Weight:
661.96
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
214-645-2
Beilstein/REAXYS Number:
2228548
MDL number:
Product Name
3′,3″,5′,5″-Tetrabromophenolphthalein ethyl ester, suitable for microscopy
InChI key
SQFXATUXPUCFFO-UHFFFAOYSA-N
InChI
1S/C22H14Br4O4/c1-2-30-22(29)14-6-4-3-5-13(14)19(11-7-15(23)20(27)16(24)8-11)12-9-17(25)21(28)18(26)10-12/h3-10,27H,2H2,1H3
SMILES string
CCOC(=O)c1ccccc1\C(c2cc(Br)c(O)c(Br)c2)=C3\C=C(Br)C(=O)C(Br)=C3
form
solid
suitability
suitable for microscopy
Quality Level
Application
3′,3″,5′,5″-Tetrabromophenolphthalein ethyl ester (TBPE) is an anionic dye used as a counter ion in the spectrophotometric determination of cationic surfactants. TBPE is also used in the spectrometric determination of aliphatic primary, secondary and tertiary amines.
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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Simple method for spectrophotometric determination of cationic surfactants without liquid-liquid extraction.
Kamaya M, et al.
Analytica Chimica Acta, 384(2), 215-218 (1999)
Simultaneous spectrophotometric analysis of aliphatic amines utilizing thermochromism of charge-transfer complexes with tetrabromophenolphthalein ethyl ester.
Sakai T, et al.
Analytical Sciences, 21(12), 1557-1560 (2005)
Spectrophotometric determination of histamine in mast cells, muscle and urine by solvent extraction with copper(II) and tetrabromophenolphthalein ethyl ester.
T Sakai et al.
The Analyst, 109(12), 1569-1572 (1984-12-01)
The application of the TBP test to bile.
E G Saker
Journal of analytical toxicology, 8(1), 51-51 (1984-01-01)
H T Chang et al.
Electrophoresis, 22(3), 394-398 (2001-03-22)
Electroelution of protein bands from a gel has advantages over the competitive common technique requiring gel sectioning with respect to yield, speed and the potential for computer-controlled application to multicomponent two-dimensional (2-D) gels. The electroelution design for the commercial high-performance
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