Fenipentol
Fenipentol Basic information
- Product Name:
- Fenipentol
- Synonyms:
-
- AURORA KA-6945
- ALPHA-BUTYLBENZYL ALCOHOL
- pc1
- PH BC
- phbc
- Phenylbutylcarbinol
- Suiclisin
- N-BUTYLPHENYLCARBINOL
- CAS:
- 583-03-9
- MF:
- C11H16O
- MW:
- 164.25
- EINECS:
- 209-493-9
- Product Categories:
-
- 583-03-9
- Mol File:
- 583-03-9.mol
Fenipentol Chemical Properties
- Melting point:
- <25 °C
- Boiling point:
- 137°C 2mm
- Density
- 0,96 g/cm3
- refractive index
- 1.5080
- Flash point:
- 137°C/2mm
- storage temp.
- Sealed in dry,Room Temperature
- pka
- 14.43±0.20(Predicted)
- form
- clear liquid
- color
- Colorless to Almost colorless
- Merck
- 14,3975
- BRN
- 1908761
- CAS DataBase Reference
- 583-03-9(CAS DataBase Reference)
- NIST Chemistry Reference
- Fenipentol(583-03-9)
- EPA Substance Registry System
- Benzenemethanol, .alpha.-butyl- (583-03-9)
Safety Information
- Safety Statements
- 24/25
- RTECS
- DN8780000
- TSCA
- Yes
- HS Code
- 2906.29.6000
MSDS
- Language:English Provider:ALFA
Fenipentol Usage And Synthesis
Aroma
Mild floral odor, slightly green, woody- barklike. One manufacturer classifies Fenipentol as "Orris-like". Useful as a fixative in Lilac or as a modifierfixative for compositions where Linalool is present.
Physical properties
White solid lumps or crystalline powder.
M.P. 69°C. B.P. 285°C.
Insoluble in water, soluble in alcohol and
oils.
Originator
Pancoral,Eisai,Japan,1973
Uses
Biliary dyskinesia;Choleretic
Production Methods
Fenipentol can be produced by reduction of Valerophenone with Sodium.
Definition
ChEBI: Fenipentol is a member of benzenes.
Manufacturing Process
The 1-phenylpentanol-(1) may be prepared in any convenient manner. Benzaldehyde may be reacted with n-butyl-magnesium bromide, and after purification 1-phenyl-pentanol-(1) is obtained in the form of a colorless oil at room temperature.
Therapeutic Function
Choleretic
Synthesis Reference(s)
Tetrahedron Letters, 25, p. 5187, 1984 DOI: 10.1016/S0040-4039(01)81559-8
Safety Profile
Poison by intraperitoneal route. Moderately toxic by ingestion and subcutaneous routes. An experimental teratogen. Other experimental reproductive effects. Stimulates the production of bile by the liver. When heated to decomposition it emits acrid smoke and irritating fumes.
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Fenipentol(583-03-9)Related Product Information
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- 5-PHENYL-1-PENTANOL
- Phenylfluorone
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- ORIENTIN
- VITEXIN-4'-RHAMNOSIDE(RG)