4-PIPERAZINOPHENOL DIHYDROBROMIDE
4-PIPERAZINOPHENOL DIHYDROBROMIDE Basic information
- Product Name:
- 4-PIPERAZINOPHENOL DIHYDROBROMIDE
- Synonyms:
-
- 1-(4-HYDROXYPHENYL)-PIPERAZINE DIHYDROBROMIDE
- 4-PIPERAZINOPHENOL DIHYDROBROMIDE
- TIMTEC-BB SBB002945
- 1-(4-Hydroxyphenyl)piperazine dihydrobromide,98%
- p-(1-piperazinyl)phenol dihydrobromide
- 4-Piperazin-1-ylphenol 2HBr
- 4-(piperazin-1-yl)phenol dihydrobroMide
- N-(4-Hydroxyphenyl)piperazine Dihydrobromide
- CAS:
- 38869-37-3
- MF:
- C10H16Br2N2O
- MW:
- 340.05
- EINECS:
- 254-164-5
- Mol File:
- 38869-37-3.mol
4-PIPERAZINOPHENOL DIHYDROBROMIDE Chemical Properties
- Melting point:
- 275 °C (decomp)
Safety Information
- Hazard Codes
- Xn
- Risk Statements
- 36/37/38-20/21/22
- Safety Statements
- 36/37/39-26-22
- RIDADR
- UN2811
- HazardClass
- 6.1
- HS Code
- 29335990
MSDS
- Language:English Provider:ACROS
4-PIPERAZINOPHENOL DIHYDROBROMIDE Usage And Synthesis
Chemical Properties
off-white to light beige or light pink
Synthesis
The preparation process for 4-Piperazinophenol dihydrobromide is as follows: Step 1: Synthesis of Dibromoethylamine hydrobromide: React diethylamine with 40% hydrogen bromide. The mixture is heated, dehydrated by fractional distillation, and excess hydrogen bromide is removed by distillation. Acetone is then added to precipitate the crystals.
Step 2: Synthesis of 4-Methoxyphenylpiperazine Dibromide: The product from Step 1 is refluxed with p-Toluidine in n-Butanol. Anhydrous sodium carbonate powder is added. Crystals are obtained upon cooling.
Step 3: Synthesis of 4-hydroxyphenylpiperazine dihydrobromide: Heat the product from Step 2 with recovered 40% hydrogen bromide solution under reflux conditions, then perform fractional distillation. Continue distillation after raising the temperature. Concentrate the distillate and add acetone to precipitate the crystals.
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