disodium 4,4'-isopropylidenediphenolate
disodium 4,4'-isopropylidenediphenolate Basic information
- Product Name:
- disodium 4,4'-isopropylidenediphenolate
- Synonyms:
-
- disodium 4,4'-isopropylidenediphenolate
- 2,2-BIS(4-HYDROXYPHENYL)PROPANE,DISODIUMSALT
- 4,4'-(1-Methylethylidene)bis[1-(sodiooxy)benzene]
- disodium 4-[2-(4-oxidophenyl)propan-2-yl]benzenolate
- 4,4'-(Dimethylmethylene)bis[1-(sodiooxy)benzene]
- 4,4'-Isopropylidenebis[1-(sodiooxy)benzene]
- Disodium 4,4'-(1-methylethylidene)diphenolate
- Disodium 4,4'-(dimethylmethylene)bisphenolate
- CAS:
- 2444-90-8
- MF:
- C15H14Na2O2
- MW:
- 272.25
- EINECS:
- 219-488-3
- Mol File:
- 2444-90-8.mol
disodium 4,4'-isopropylidenediphenolate Chemical Properties
- storage temp.
- Inert atmosphere,Room Temperature
- Appearance
- White to off-white Solid
- EPA Substance Registry System
- Phenol, 4,4'-(1-methylethylidene)bis-, sodium salt (1:2) (2444-90-8)
Safety Information
- TSCA
- TSCA listed
- Hazardous Substances Data
- 2444-90-8(Hazardous Substances Data)
disodium 4,4'-isopropylidenediphenolate Usage And Synthesis
Hazard
Moderately toxic by ingestion and skin con- tact. A moderate skin and severe eye irritant.
Synthesis
80-05-7
2444-90-8
General procedure: 0.01 mole of bisphenol A, 0.02 mole of NaOH and 150 ml of 10% aqueous K2CO3 were added to a 250 ml three-necked flask, and nitrogen was passed through to displace the oxygen in the flask. The reaction mixture was stirred and reacted at 100 °C for 1 hour to produce a precipitate. The precipitate was collected by filtration under nitrogen protection, washed twice with 30 mL of hot isopropanol, and subsequently dried under reduced pressure at 200°C for 3 hours to give 25.8 g of bisphenol A disodium salt in 95% yield. Example 27: 0.01 moles of bisphenol A, 0.02 moles of NaOH and 150 mL of 35% K2CO3 aqueous solution were added to a 250 mL three-necked flask, and nitrogen was passed through to displace the oxygen in the flask. The reaction mixture was stirred and reacted at 100 °C for 1 h to produce a precipitate. The precipitate was collected by filtration under nitrogen protection, washed twice with 30 mL of hot isopropanol, and subsequently dried under reduced pressure at 200 °C for 3 hours to give 25.8 g of bisphenol A disodium salt in 95% yield.
References
[1] Patent: US2005/272957, 2005, A1. Location in patent: Page/Page column 4-5
[2] Patent: US2005/272957, 2005, A1. Location in patent: Page/Page column 4
[3] Patent: US2005/272957, 2005, A1. Location in patent: Page/Page column 2
[4] Patent: US2005/272957, 2005, A1. Location in patent: Page/Page column 4
[5] Patent: US2005/272957, 2005, A1. Location in patent: Page/Page column 3
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