trihydroxytriphenylmethane

trihydroxytriphenylmethane - Names and Identifiers

Name	Trihydroxytriphenylmethane
Synonyms	4fdp BIP-PHBZ BisP-PHBA AV Lite BIP-PHBZ Trihydroxytriphenylmethane trihydroxytriphenylmethane TRIS(4-HYDROXYPHENYL)METHANE 4,4',4'-METHANETRIYLTRIPHENOL 4,4',4''-methanetriyltriphenol 4,4,4-Trihydroxytriphenylmethane 4,4',4''-Trihydroxytriphenylmethane 4-[bis(4-hydroxyphenyl)methyl]phenol
CAS	603-44-1
EINECS	210-040-2
InChI	InChI=1/C19H16O3/c20-16-7-1-13(2-8-16)19(14-3-9-17(21)10-4-14)15-5-11-18(22)12-6-15/h1-12,19-22H
InChIKey	WFCQTAXSWSWIHS-UHFFFAOYSA-N

trihydroxytriphenylmethane - Physico-chemical Properties

Molecular Formula	C19H16O3
Molar Mass	292.33
Density	1.282±0.06 g/cm3(Predicted)
Melting Point	247 °C
Boling Point	503.8±45.0 °C(Predicted)
Flash Point	239.6°C
Solubility	soluble in Methanol
Vapor Presure	8.98E-11mmHg at 25°C
Appearance	powder to crystal
Color	Light yellow to Yellow to Orange
pKa	9.83±0.10(Predicted)
Storage Condition	Inert atmosphere,Room Temperature
Refractive Index	1.674
MDL	MFCD00191589

trihydroxytriphenylmethane - Introduction

Trihydroxytriphenylmethane is an organic compound structurally containing three hydroxyl groups and three toluene groups. Its molecular formula is C19H18O3 and its relative molecular mass is 294.35g/mol.

nature, Trihydroxytriphenylmethane is a colorless crystal or white powder, not soluble in water, soluble in alcohol, ether and other organic solvents. It is stable at room temperature and can be stored for a long time.

The main use of this compound is as a synthetic intermediate for organic polymer materials. Because it contains many hydroxyl groups in the molecule, it can react with other compounds, esterification, acylation and other reactions to generate polymer compounds with different functions. Common applications include synthetic resins, coatings, plastics, rubbers, dyes, etc.

The method for preparing Trihydroxytriphenylmethane is usually obtained by oxidizing trimethylbenzene. A common synthetic method is to react mesitylene with hydrogen peroxide under acidic conditions to form Trihydroxytriphenylmethane. The reaction conditions need to be properly controlled to avoid side reactions.

In terms of safety information, Trihydroxytriphenylmethane is a general organic compound with low acute toxicity to human body. However, as a synthetic intermediate of polymer materials, it is necessary to follow the safe operation specifications of chemicals. During use, care should be taken to avoid contact with skin and eyes, and to avoid inhaling its dust or vapor. If accidentally contact, should immediately rinse with water, and timely medical treatment. During storage and transportation, avoid mixing with oxidants, strong acids and other substances to prevent unsafe conditions. It should be noted that the safety information provided in this article is for reference only, please operate according to the safety data sheet of the actual material.

Last Update：2024-04-10 22:30:50