Name | P-xylenolphthaleine |
Synonyms | p-Xylenolphthalein P-XYLENOLPHTHALEIN P-xylenolphthaleine p-xylenolphthalein (pH 9.0-10.5) 2',5',2'',5''-TETRAMETHYLPHENOLPHTHALEIN 3,3-bis(4-hydroxy-2,5-dimethylphenyl)-2-benzofuran-1(3H)-one 3,3-Bis(4-hydroxy-2,5-dimethylphenyl)isobenzofuran-1(3H)-one 3,3-Bis(4-hydroxy-2,5-dimethylphenyl)-1(3H)-isobenzofuranone 3,3-Bis(2,5-dimethyl-4-hydroxyphenyl)isobenzofuran-1(3H)-one 4,4'-[(3-Oxo-1,3-dihydroisobenzofuran)-1,1-diyl]bis(2,5-dimethylphenol) |
CAS | 50984-88-8 |
EINECS | 256-893-4 |
InChI | InChI=1/C24H22O4/c1-13-11-21(25)15(3)9-19(13)24(20-10-16(4)22(26)12-14(20)2)18-8-6-5-7-17(18)23(27)28-24/h5-12,25-26H,1-4H3 |
Molecular Formula | C24H22O4 |
Molar Mass | 374.43 |
Density | 1.270±0.06 g/cm3(Predicted) |
Melting Point | 276°C |
Boling Point | 569.6±50.0 °C(Predicted) |
Flash Point | 198.4°C |
Solubility | Solubility Insoluble in water; soluble in ethanol, acetone |
Vapor Presure | 1.41E-13mmHg at 25°C |
Appearance | powder |
Color | Pale yellow or cream-colored |
BRN | 346799 |
pKa | 9.7(at 25℃) |
Storage Condition | Inert atmosphere,Room Temperature |
Refractive Index | 1.649 |
MDL | MFCD00042785 |
WGK Germany | 3 |
application | dimethylphenolphthalein can also be used as a color-changing component of children's color-changing toothpaste, and can also be used in extraction photometry for the detection of p-chloroethyl sulfur, which has important application prospects. |
preparation | a preparation method of p-diphenolphthalein, comprising the following steps: S1, using 2 parts of p-xylene phenol and 1 part of phthalic anhydride as raw materials in molar parts, 5.5 parts of polyphosphoric acid and 0.1 parts of powdered aluminum trichloride were added for condensation reaction to obtain a mixed solution containing p-diphenolphthalein, in which the condensation reaction temperature was 70 ℃, and the condensation reaction time was 3.5h; S2, the mixed solution containing p-diphenolphthalein was cooled, and water was added for quenching reaction, in which the weight ratio of water to xylenol was 9.5:1, and the crude product was obtained by filtration; the crude and activated carbon are added to 95% ethanol for heating and reflux for 1h, then hot filtration and decolorization, cooling and crystallization, and drying to obtain p-methylphenolphthalein. |