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111309

Sigma-Aldrich

1-Phenyl-1-propanol

≥97%

Synonym(e):

α-Ethylbenzylalkohol, (±)-1-Phenylpropanol

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About This Item

Lineare Formel:
C2H5CH(C6H5)OH
CAS-Nummer:
93-54-9
Molekulargewicht:
136.19
Beilstein:
1906759
EG-Nummer:
202-256-0
MDL-Nummer:
MFCD00004564
UNSPSC-Code:
12352100
eCl@ss:
39023126
PubChem Substanz-ID:
24847022
NACRES:
NA.22

Assay

≥97%

Brechungsindex

n20/D 1.52 (lit.)

bp

103 °C/14 mmHg (lit.)

Dichte

0.994 g/mL at 25 °C (lit.)

SMILES String

CCC(O)c1ccccc1

InChI

1S/C9H12O/c1-2-9(10)8-6-4-3-5-7-8/h3-7,9-10H,2H2,1H3

InChIKey

DYUQAZSOFZSPHD-UHFFFAOYSA-N

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Allgemeine Beschreibung

1-Phenyl-1-propanol enantiomers (E-PP) forms the inclusion complexes of cyclic decapeptide (CDP) which were studied using the density functional theory (DFT) B3LYP method. It was also used to determine the mass transfer kinetics effect on the elution profiles of the 1-phenyl-1-propanol (PP) enantiomers on Chiracel OB (cellulose tribenzoate coated on silica gel).

Piktogramme

Exclamation mark
GHS07

Signalwort

Warning

H-Sätze

H302

Gefahreneinstufungen

Acute Tox. 4 Oral

Lagerklassenschlüssel

10 - Combustible liquids

WGK

WGK 3

Flammpunkt (°F)

194.0 °F - closed cup

Flammpunkt (°C)

90 °C - closed cup

Persönliche Schutzausrüstung

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

Analysenzertifikate (COA)

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Sigma-Aldrich

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Sigma-Aldrich

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Stefan Ottiger et al.
Journal of chromatography. A, 1162(1), 74-82 (2007-02-17)
The separation of the enantiomers of 1-phenyl-1-propanol by supercritical fluid chromatography on a chiral stationary phase, which consists of cellulose tris (3,5-dimethylphenylcarbamate) coated on a silica support (Chiralcel-OD), is studied under overloaded, non-linear chromatographic conditions. Pulse experiments are performed at
Arvind Rajendran et al.
Journal of chromatography. A, 1092(1), 55-64 (2005-09-29)
The enantioseparation of 1-phenyl-1-propanol through the supercritical fluid-simulated moving bed (SF-SMB) process is studied. Non-linear isotherms were measured on an analytical column, and used together with the triangle theory for SMB design to select operating conditions for the SF-SMB. Experiments
Hongge Zhao et al.
Journal of molecular modeling, 18(3), 851-858 (2011-06-01)
Cyclic peptides are exciting novel hosts for chiral and molecular recognition. In this work, the inclusion complexes of cyclic decapeptide (CDP) with the 1-phenyl-1-propanol enantiomers (E-PP) are firstly studied using the density functional theory (DFT) B3LYP method. Our calculated results
S Khattabi et al.
Journal of chromatography. A, 877(1-2), 95-107 (2000-06-14)
Using single-step frontal analysis, we measured single-component and competitive adsorption isotherm data for the two enantiomers of 1-phenyl-1-propanol (PP). These experimental data were fitted to several competitive bi-Langmuir models (with 8, 6, 5 and 4 parameters) and to the competitive
Pieter Saveyn et al.
Langmuir : the ACS journal of surfaces and colloids, 25(19), 11322-11327 (2009-09-03)
The influence of the physicochemical properties of the vesicular bilayer on the sorption of poorly water soluble compounds was investigated with pulsed field gradient 1H nuclear magnetic resonance (PFG-NMR) for the case of phosphatidylcholine and dioctadecyldimethylammonium bromide (DODAB), using 4-ethylbenzyl
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