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Fenipentol

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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
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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)
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Safety Information

Safety Statements 
24/25
RTECS 
DN8780000
TSCA 
Yes
HS Code 
2906.29.6000

MSDS

  • Language:English Provider:ALFA
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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.

FenipentolSupplier

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