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Merck

W288403

Sigma-Aldrich

1-Phenyl-1-propanol

≥97%, FG

Sinónimos:

α-Ethylbenzyl alcohol, (±)-1-Phenylpropanol

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About This Item

Fórmula lineal:
C2H5CH(C6H5)OH
Número de CAS:
Peso molecular:
136.19
FEMA Number:
2884
Beilstein/REAXYS Number:
1906759
EC Number:
Council of Europe no.:
82
MDL number:
UNSPSC Code:
12164502
eCl@ss:
39023126
PubChem Substance ID:
Flavis number:
2.033
NACRES:
NA.21

biological source

synthetic

Quality Level

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

signalword

Warning

hcodes

Hazard Classifications

Acute Tox. 4 Oral

Storage Class

10 - Combustible liquids

wgk_germany

WGK 3

flash_point_f

194.0 °F - closed cup

flash_point_c

90 °C - closed cup

ppe

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


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Visite la Librería de documentos

Encyclopedia of Food and Color Additives, 1, 2196-2196 (1997)
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]
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

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