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Thymolphthalein
[CAS# 125-20-2]

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Complete supplier list of Thymolphthalein
Identification
Classification Biochemical >> Biochemical reagent >> Acid-base indicator
Name Thymolphthalein
Synonyms 3,3-Bis(4-hydroxy-5-isopropyl-o-tolyl)phthalide
Molecular Structure CAS # 125-20-2, Thymolphthalein, 3,3-Bis(4-hydroxy-5-isopropyl-o-tolyl)phthalide
Molecular Formula C28H30O4
Molecular Weight 430.54
CAS Registry Number 125-20-2
EC Number 204-729-7
SMILES CC1=CC(=C(C=C1C2(C3=CC=CC=C3C(=O)O2)C4=CC(=C(C=C4C)O)C(C)C)C(C)C)O
Properties
Solubility insoluble (water), soluble (alcohol, acetone, dilute alkalies, H2SO4) (Expl.)
Density 1.2±0.1 g/cm3, Calc.*, 0.92 g/mL (Expl.)
Melting point 251-253 ºC (Expl.)
Index of Refraction 1.613, Calc.*
Boiling Point 571.6±50.0 ºC (760 mmHg), Calc.*
Flash Point 187.5±23.6 ºC, Calc.*
* Calculated using Advanced Chemistry Development (ACD/Labs) Software.
Safety Data
Hazard Symbols symbol   GHS08 Danger    Details
Hazard Statements H341-H350-H361    Details
Precautionary Statements P203-P280-P318-P405-P501    Details
Hazard Classification
up    Details
HazardClassCategory CodeHazard Statement
Reproductive toxicityRepr.2H361
CarcinogenicityCarc.1BH350
Germ cell mutagenicityMuta.2H341
Acute hazardous to the aquatic environmentAquatic Acute1H400
Acute toxicityAcute Tox.4H302
Chronic hazardous to the aquatic environmentAquatic Chronic4H413
SDS Available
up Discovory and Applicatios
Thymolphthalein is a chemical compound commonly used as a pH indicator. It was first synthesized in the early 20th century through the condensation reaction of thymol with phthalic anhydride in the presence of a strong acid catalyst. This synthesis method is similar to the process used for creating other phthalein-based indicators such as phenolphthalein. Thymolphthalein’s structure consists of two thymol groups linked by a central phthalic structure, giving it distinct color-changing properties.

The primary method for synthesizing thymolphthalein involves the reaction of thymol with phthalic anhydride under acidic conditions. The resulting product is then purified and recrystallized to obtain the final indicator compound. This synthesis pathway is efficient and widely used in laboratories and industrial settings.

Thymolphthalein is best known for its application as a pH indicator. It is colorless in acidic to neutral solutions and turns a deep blue in basic conditions, specifically within a pH range of 9.3 to 10.5. This makes it useful for titrations in analytical chemistry where the detection of alkaline conditions is required. It is also employed in educational demonstrations and laboratory experiments to illustrate the concept of acid-base reactions.

Apart from its use as a pH indicator, thymolphthalein is used in invisible ink formulations. When dissolved in alcohol and applied to paper, the writing remains invisible until exposed to a basic solution, which reveals the blue color. This property has been utilized for security and novelty applications.

In industrial applications, thymolphthalein is sometimes used in chemical sensors and diagnostic tools where accurate pH detection is critical. Its stability and clear color transition make it a reliable choice for monitoring pH changes in various chemical processes. Ongoing research into new applications continues to expand its utility in analytical and applied chemistry.
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