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W288403

Sigma-Aldrich

1-Phenyl-1-propanol

≥97%, FG

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Synonym(s):
α-Ethylbenzyl alcohol, (±)-1-Phenylpropanol
Linear Formula:
C2H5CH(C6H5)OH
CAS Number:
93-54-9
Molecular Weight:
136.19
FEMA Number:
2884
Beilstein:
1906759
EC Number:
202-256-0
Council of Europe no.:
82
MDL number:
MFCD00004564
UNSPSC Code:
12164502
eCl@ss:
39023126
PubChem Substance ID:
24901372
Flavis number:
2.033
NACRES:
NA.21

biological source

synthetic

Quality Level

400

grade

FG

Agency

meets purity specifications of JECFA

reg. compliance

EU Regulation 1334/2008 & 178/2002
FDA 21 CFR 172.515

Assay

≥97%

refractive index

n20/D 1.52 (lit.)

bp

103 °C/14 mmHg (lit.)

density

0.994 g/mL at 25 °C (lit.)

application(s)

flavors and fragrances

Documentation

see Safety & Documentation for available documents

food allergen

no known allergens

Organoleptic

balsam; floral; sweet

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

InChI key

DYUQAZSOFZSPHD-UHFFFAOYSA-N

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General description

1-Phenyl-1-propanol is a secondary alcohol that can be used as a flavoring agent.

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H302

Hazard Classifications

Acute Tox. 4 Oral

WGK

WGK 3

Flash Point(F)

closed cup

Flash Point(C)

closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Encyclopedia of Food and Color Additives, 1, 2196-2196 (1997)
Arvind Rajendran et al.
Journal of chromatography. A, 1076(1-2), 183-188 (2005-06-25)
The supercritical fluid chromatography (SFC) separation of the enantiomers of 1-phenyl-1-propanol on the chiral stationary phase Chiralcel OD under linear conditions is studied. Supercritical CO2 modified with methanol is used as a mobile phase. The effect of modifier concentration, pressure
Anna M Costa et al.
Journal of the American Chemical Society, 124(24), 6929-6941 (2002-06-13)
The optimization of asymmetric catalysts for enantioselective synthesis has conventionally revolved around the synthesis and screening of enantiopure ligands. In contrast, we have optimized an asymmetric reaction by modification of a series of achiral ligands. Thus, employing (S)-3,3'-diphenyl BINOL [(S)-Ph(2)-BINOL]
Encyclopedia of Food and Color Additives, 1, 2196-2196 (1997)
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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