| Weight | 430.544 g/mol |
|---|---|
| Formula | C28H30O4 |
| Hydrogen Acceptors | 4 |
| Hydrogen Donors | 2 |
| Aromatic Rings | 3 |
| Rotatable Bonds | 4 |
THYMOLPHTHALEIN (125-20-2)
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- Sodium Thymolphthalein Monophosphate: A New Acid Phosphatase Substrate with Greater Specificity for the Prostatic Enzyme in Serum (Clinical Chemistry, 1971)
- Rapid method for determining alkaline phosphatase activity in serum with thymolphthalein monophosphate. (Clinical Chemistry, 1970)
- The synthesis of thymolphthalein monophosphate, a new substrate for alkaline phosphatase. (Clinica Chimica Acta, 1966)
- Polarographic reduction of phenolphthalein, cresolphthalein, thymolphthalein, and -naphtholphthalein in aqueous and nonaqueous ethanolic solutions (Canadian Journal of Chemistry, 1979)
- Improved determination of prostatic acid phosphatase (sodium thymolphthalein monophosphate substrate). (Clinical Chemistry, 1976)
- A clinical assay for prostatic acid phosphatase using choline phosphate as a substrate: Comparison with thymolphthalein phosphate (The Prostate, 1981)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCC1=CC(=C(C=C1C2(C3=CC=CC=C3C(=O)O2)C4=CC(=C(C=C4C)O)C(C)C)C(C)C)O
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InChIKeyLDKDGDIWEUUXSH-UHFFFAOYSA-N
- Pubchem - THYMOLPHTHALEIN
- Wikipedia - thymolphthalein
Thymolphthalein is an acidbase (pH) indicator. Its transition range is around pH 9.310.5. Below this pH, it is colorless; above, it is blue.
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Synthesis
THYMOL
+
Reactant
(Friedel-Crafts alkylation)
benzoic acid
+
Reactant
(Ester from carboxilic acid(SN2))
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THYMOLPHTHALEIN
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