| Weight | 466.599 g/mol |
|---|---|
| Formula | C27H30O5S |
| Hydrogen Acceptors | 5 |
| Hydrogen Donors | 2 |
| Aromatic Rings | 3 |
| Rotatable Bonds | 4 |
Thymol blue (76-61-9)
thymolsulfonphthalein · thymol blue, monosodium salt
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- Spectrophotometric pH measurements of surface seawater at in-situ conditions: absorbance and protonation behavior of thymol blue (Marine Chemistry, 1996)
- Fibre-optic pesticide biosensor based on covalently immobilized acetylcholinesterase and thymol blue. (Talanta, 1997)
- Enhanced photocatalytic degradation of methyl red and thymol blue using titaniaaluminazinc ferrite nanocomposite (Applied Catalysis B-environmental, 2011)
- Spectrophotometric pH measurement in estuaries using thymol blue and m-cresol purple (Marine Chemistry, 2004)
- On-line solid phase selective separation and preconcentration of Cd(II) by solid-phase extraction using carbon active modified with methyl thymol blue. (Journal of Hazardous Materials, 2007)
- Selectivity enhancement in spectrophotometry: on-line interference suppression using polyurethane foam minicolumn for aluminum determination with Methyl Thymol Blue (Analyst, 1999)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - thymolsulfonphthalein
- thymol blue, monosodium salt
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SMILESCC1=CC(=C(C=C1C2(C3=CC=CC=C3S(=O)(=O)O2)C4=CC(=C(C=C4C)O)C(C)C)C(C)C)O
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InChIKeyPRZSXZWFJHEZBJ-UHFFFAOYSA-N
- Pubchem - Thymol blue
- Wikipedia - thymol blue
Thymol blue (thymolsulphonephthalein) is a brownish-green or reddish-brown crystalline powder that is used as a pH indicator. It is insoluble in water but soluble in alcohol and dilute alkali solutions. It transitions from red to yellow at pH 1.22.8 and from yellow to blue at pH 8.09.6.
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Synthesis
THYMOL
+
Reactant
(Friedel-Crafts alkylation)
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Thymol blue
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