- Febuprol
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- $1980.00 / 50mg
-
2024-10-28
- CAS:3102-00-9
- Min. Order:
- Purity:
- Supply Ability: 10g
- Febuprol
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- $1.00 / 1KG
-
2024-08-11
- CAS:3102-00-9
- Min. Order: 1KG
- Purity: 99%
- Supply Ability: 20T
- Febuprol
-
- $1.00 / 1KG
-
2019-07-06
- CAS:3102-00-9
- Min. Order: 1G
- Purity: 98%
- Supply Ability: 100KG
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| | Febuprol Basic information |
| Product Name: | Febuprol | | Synonyms: | (3-n-butoxy-2-hydroxypropyl)phenylether;1-butoxy-3-phenoxy-2-propano;1-butoxy-3-phenoxy-2-propanol;3-n-butoxy-1-phenoxy-2-propanol;h-33;k-10033;1-butoxy-3-(phenoxy)propan-2-ol;FEBUPROL | | CAS: | 3102-00-9 | | MF: | C13H20O3 | | MW: | 224.3 | | EINECS: | 221-454-8 | | Product Categories: | API | | Mol File: | 3102-00-9.mol |  |
| | Febuprol Chemical Properties |
| Melting point | 25°C | | Boiling point | bp11 165°; bp1.0 125-132° | | density | d420 1.027 | | refractive index | nD20 1.5004 | | storage temp. | 2-8°C | | form | Liquid | | color | Colorless to light yellow | | CAS DataBase Reference | 3102-00-9(CAS DataBase Reference) |
| Toxicity | LD50 in mice, rats (mg/kg): 3050, 2370 orally; 436, 400 i.p. (Hofrichter) |
| | Febuprol Usage And Synthesis |
| Originator | Valbil,Rohm Pharma,W. Germany,1981 | | Definition | ChEBI: Febuprol is an aromatic ether. | | Manufacturing Process | Initially, 4.5 g (0.08 mol) pulverized potassium hydroxide was dissolved in
300 ml isopropanol in a 500 ml four-neck flask equipped with stirrer, intensive
cooler, dropping funnel and feed pipe for the gas treatment with nitrogen.
Then, 52.0 g (0.4 mol) n-butylglycidyl ether and 41.4 g (0.44 mol) phenol
was added thereto, whereafter the material was heated to boiling under
nitrogen. The material was stirred, about 8.5 hours, until no glycidyl ether
could be determined, e.g., by gas chromatography.
After the suspension was cooled under nitrogen, the solvent was distilled off
under vacuum. The residue was taken up in 200 ml water and the milky
emulsion extracted exhaustively with ether. From the organic phase, the
excess butylglycidyl ether was extracted with diluted potassium hydroxide
solution. The ether phase was washed neutral with water and the solvent
removed after drying with sodium sulfate. The remaining oily residue was
distilled under vacuum; there was obtained a colorless liquid of BP
123.5°C/0.07 mm. Yield: 81.8 g (91.1% of the theory) | | Therapeutic Function | Choleretic |
| | Febuprol Preparation Products And Raw materials |
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