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4-Phenyl-2-butanol

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4-Phenyl-2-butanol Basic information

Product Name:
4-Phenyl-2-butanol
Synonyms:
  • 4-Phenylbutan-2-ol
  • alpha-methyl-benzenepropano
  • AURORA KA-6974
  • FEMA 2879
  • ALPHA-METHYL-BENZENEPROPANOL
  • (+/-)-4-PHENYL-2-BUTANOL
  • 4-PHENYL-2-BUTANOL
  • PHENYLETHYL METHYL CARBINOL
CAS:
2344-70-9
MF:
C10H14O
MW:
150.22
EINECS:
219-055-9
Product Categories:
  • 11
Mol File:
2344-70-9.mol
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4-Phenyl-2-butanol Chemical Properties

Melting point:
61 °C
Boiling point:
132 °C/14 mmHg (lit.)
Density 
0.970 g/mL at 25 °C (lit.)
refractive index 
n20/D 1.5140(lit.)
FEMA 
2879 | 4-PHENYL-2-BUTANOL
Flash point:
231 °F
storage temp. 
Sealed in dry,Room Temperature
solubility 
Almost insoluble in water, soluble in alcohol and oils
pka
15.10±0.20(Predicted)
form 
liquid
color 
Colorless
Odor
at 100.00 %. floral peony foliage sweet mimosa heliotrope
Odor Type
floral
JECFA Number
815
BRN 
1908294
LogP
2.23
CAS DataBase Reference
2344-70-9(CAS DataBase Reference)
NIST Chemistry Reference
4-Phenyl-2-butanol(2344-70-9)
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Safety Information

Safety Statements 
24/25
WGK Germany 
3
HS Code 
29062900

MSDS

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4-Phenyl-2-butanol Usage And Synthesis

Chemical Properties

CLEAR COLOURLESS LIQUID

Chemical Properties

4-Phenyl-2-butanol has a herbaceous, aromatic, floral-fruity odor.

Uses

4-Phenyl-2-butanol is a reagent used for the direct alkylation of amines with primary and secondary alcohols through biocatalytic hydrogen borrowing. It is also used in the preparation of personal care composition comprising malodor reduction compositions.

Preparation

The optically inactive product can be prepared by hydrogenation of benzylidene acetone in alcohol solution; under pressure in the presence of platinum oxide, palladium oxide or ferrous sulfate; by reduction with magnesium in methanol.

Synthesis Reference(s)

Tetrahedron Letters, 30, p. 6461, 1989 DOI: 10.1016/S0040-4039(01)88994-2

General Description

4-Phenyl-2-butanol undergoes (η5-pentaphenylcyclopentadienyl)RuCl(CO)2 catalyzed racemization efficiently at room temperature in the presence of a base. 4-Phenyl-2-butanol on reaction with sulfuric acid yields polymer.

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