| Identification | More | [Name]
4-Phenyl-2-butanol | [CAS]
2344-70-9 | [Synonyms]
(+/-)-4-PHENYL-2-BUTANOL
4-PHENYL-2-BUTANOL
ALPHA-METHYL-BENZENEPROPANOL
AURORA KA-6974
FEMA 2879
PHENYLETHYL METHYL CARBINOL
4-Phenylbutan-2-ol
alpha-methyl-benzenepropano
Phenylbutanol
4-Phenyl-2-butanol, 99+%
Benzenepropanol, .alpha.-methyl-
α-methyl-benzenepropanol
4-PHENYL-2-BUTANOL 98%
4-Phenyl-2-butanol, 98% (B25414 duplicate|)
1-Methyl-3-phenyl-1-propanol
1-Phenyl-3-butanol
2-Hydroxy-4-phenylbutane
a-Methylbenzenepropanol
1-Phenethylethanol
α-Methylbenzene(1-propanol) | [EINECS(EC#)]
219-055-9 | [Molecular Formula]
C10H14O | [MDL Number]
MFCD00044349 | [Molecular Weight]
150.22 | [MOL File]
2344-70-9.mol |
| Chemical Properties | Back Directory | [Appearance]
CLEAR COLOURLESS LIQUID | [Melting point ]
61 °C | [Boiling point ]
132 °C/14 mmHg (lit.) | [density ]
0.970 g/mL at 25 °C(lit.)
| [FEMA ]
2879 | [refractive index ]
n20/D 1.5140(lit.)
| [Fp ]
231 °F
| [storage temp. ]
Sealed in dry,Room Temperature | [solubility ]
Almost insoluble in water, soluble in alcohol and oils | [form ]
liquid
| [pka]
15.10±0.20(Predicted) | [color ]
Colorless | [Odor]
at 100.00 %. floral peony foliage sweet mimosa heliotrope | [Odor Type]
floral | [JECFA Number]
815 | [BRN ]
1908294 | [InChI]
1S/C10H14O/c1-9(11)7-8-10-5-3-2-4-6-10/h2-6,9,11H,7-8H2,1H3 | [InChIKey]
GDWRKZLROIFUML-UHFFFAOYSA-N | [SMILES]
CC(O)CCc1ccccc1 | [LogP]
2.23 | [CAS DataBase Reference]
2344-70-9(CAS DataBase Reference) | [NIST Chemistry Reference]
4-Phenyl-2-butanol(2344-70-9) |
| Safety Data | Back Directory | [Safety Statements ]
S24/25:Avoid contact with skin and eyes . | [WGK Germany ]
3
| [HS Code ]
29062900 | [Storage Class]
10 - Combustible liquids |
| Hazard Information | Back Directory | [Chemical Properties]
4-Phenyl-2-butanol has a herbaceous, aromatic, floral-fruity odor. | [Chemical Properties]
CLEAR COLOURLESS LIQUID | [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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