W288403
1-苯基-1-丙醇
≥97%, FG
别名:
α-苯丙醇, (±)-1-苯丙醇
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关于此项目
线性分子式:
C2H5CH(C6H5)OH
化学文摘社编号:
分子量:
136.19
FEMA Number:
2884
Council of Europe no.:
82
UNSPSC Code:
12164502
eCl@ss:
39023126
PubChem Substance ID:
Flavis number:
2.033
EC Number:
202-256-0
NACRES:
NA.21
MDL number:
Beilstein/REAXYS Number:
1906759
Organoleptic:
balsam; floral; sweet
Grade:
FG
Biological source:
synthetic
Agency:
meets purity specifications of JECFA
Food allergen:
no known allergens
产品名称
1-苯基-1-丙醇, ≥97%, FG
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
biological source
synthetic
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
Quality Level
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General description
1-苯基-1-丙醇是可用作调味剂的仲醇。
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral
存储类别
10 - Combustible liquids
wgk
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
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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