| Identification | Back Directory | [Name]
1,1-BIS(4-HYDROXYPHENYL)-3,3,5-TRIMETHYLCYCLOHEXANE | [CAS]
129188-99-4 | [Synonyms]
BPTMC
BISP-TMC
Bisphenol TMC
Bisphenol TMC,BPTMC
Bisphenol TMC Solution
Bisphenol TMC@10 mg/mL in Methanol
4,4'-(3,3,5-Trimethylcyclohexylidene)diphenol
4,4'-(3,3,5-Trimethylcyclohexylidene)bisphenol
Bis(4-hydroxyphenyl)-3,3,5-triMethylcyclohexane
Phenol,4,4'-(3,3,5-trimethylcyclohexylidene)bis-
4,4'-(3,3,5-Trimethylcyclohexane-1,1-diyl)diphenol
3,3,5-TriMethyl-1,1-bis(4-hydroxyphenyl)cyclohexane
1,1-BIS(4-HYDROXYPHENYL)-3,3,5-TRIMETHYLCYCLOHEXANE
4,4'-(3,3,5-Trimethyl-1,1-cyclohexanediyl)bisphenol
4,4'-(3,3,5-Trimethylcyclohexane-1,1-diyl)bisphenol
4-[1-(4-hydroxyphenyl)-3,3,5-trimethylcyclohexyl]phenol
1,1-BIS(4-HYDROXYPHENYL)PROPANEBIS(2-HYDROXYPROPYL)ETHER | [EINECS(EC#)]
603-320-4 | [Molecular Formula]
C21H26O2 | [MDL Number]
MFCD28167155 | [MOL File]
129188-99-4.mol | [Molecular Weight]
310.43 |
| Hazard Information | Back Directory | [Description]
Bisphenol TMC, also known as 2,2-bis-(4-hydroxy phenyl) butane, chemical structural formula is , be very important organic chemistry raw material, they are as macromolecular material intermediate, are applied in the fields such as synthetic epoxy resin, cyanate, polycarbonate, polyarylester and resol widely. | [Uses]
Bisphenol TMC(1,1-Bis(4-hydroxyphenyl)-3,3,5-trimethylcyclohexane) is a bisphenol derivative used in the preparation of polycarbonate, polyester and epoxy resins.
| [Synthesis]
The synthesis of 1,1-BIS(4-HYDROXYPHENYL)-3,3,5-TRIMETHYLCYCLOHEXANE is as follows:112.8 g (1.2 mol) of phenol, 16.9 g of water, 0.5 g of 75% aqueous solution of phosphoric acid and 7.2 g of BPTMCP crystals were placed in a one liter capacity four-necked flask provided with a thermometer, a dropping funnel, a reflux condenser and a stirrer to prepare a slurry. The slurry was adjusted at a temperature of 20° C. After the inside the flask was replaced by nitrogen gas, hydrogen chloride gas was introduced into the flask under stirring. The gas composition in the reaction vessel was analyzed and the volume concentration of hydrogen chloride gas was adjusted at 80%. 4.2 g of 15% aqueous solution of sodium methyl mercaptide was added dropwise to the slurry while the slurry was maintained at a temperature of 20° C., and then a mixture of 112.8 g (1.2 mol) of phenol and 42.0 g (0.3 mol) of TMC was added dropwise to the slurry over a period of six hours. The reaction mixture was found to increase in temperature during the addition, and when the addition was completed, the temperature was found to be 40° C. Then, the reaction was further continued at a temperature of 40° C. for anther three hours under stirring until completion. The reaction mixture was found to be slurry throughout the reaction from the start of the reaction when the mixture of phenol and TMC was added dropwise to the slurry to the completion of the reaction. The resulting reaction mixture was analyzed by liquid chromatography. The production yield (mol of BPTMC produced/mol of starting TMC used) was found 92.9%.
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