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제품정보 (DICE 배송 시 비용 별도)
Linear Formula:
CH3CH2CH2OH
CAS 번호:
Molecular Weight:
60.10
EC Number:
200-746-9
UNSPSC Code:
12352001
PubChem Substance ID:
Beilstein/REAXYS Number:
1098242
MDL number:
Assay:
99.7%
Grade:
anhydrous
Vapor pressure:
10 mmHg ( 147 °C), 14.9 mmHg ( 20 °C)
InChI key
BDERNNFJNOPAEC-UHFFFAOYSA-N
InChI
1S/C3H8O/c1-2-3-4/h4H,2-3H2,1H3
SMILES string
CCCO
grade
anhydrous
Quality Level
vapor pressure
10 mmHg ( 147 °C), 14.9 mmHg ( 20 °C)
assay
99.7%
form
liquid
autoignition temp.
700 °F
expl. lim.
13.7 %
impurities
<0.005% water
evapn. residue
<0.0003%
refractive index
n20/D 1.384 (lit.)
pH
8.5 (20 °C, 200 g/L)
mp
−127 °C (lit.)
density
0.804 g/mL at 25 °C (lit.)
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Application
1-Propanol may be used as a starting material in the vapour-phase synthesis of 2-propylphenol and 3-pentanone over CeO2-MgO and CeO2-Fe2O3 catalysts, respectively. It may also be used as a solvent for the palladium catalyzed cross-coupling of boronic acids with aryl halides to form biaryls.
signalword
Danger
hcodes
Hazard Classifications
Eye Dam. 1 - Flam. Liq. 2 - STOT SE 3
target_organs
Central nervous system
저장 등급
3 - Flammable liquids
wgk
WGK 1
flash_point_f
71.6 °F - closed cup
flash_point_c
22 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
Ortho-selective alkylation of phenol with 1-propanol catalyzed by CeO2-MgO
Sato S, et al
J. Catal., 184(1), 180-188 (1999)
Synthesis of unsymmetrical biaryls using a modified Suzuki cross-coupling: 4-biphenylcarboxaldehyde
Bret EH, et al.
Organic Syntheses, 75, 53-53 (1998)
Synthesis of 3-pentanone from 1-propanol over CeO2-Fe2O3 catalysts
Kamimura Y, et al
Applied Catalysis A: General, 252(2), 399-410 (2003)
Mesoporous alumina (I): comparison of synthesis schemes using anionic, cationic, and non-ionic surfactants.
Ray JC, et al.
Microporous and Mesoporous Materials : The Official Journal of the International Zeolite Association, 100(1), 183-190 (2007)
Dynamics of glass-forming liquids. III. Comparing the dielectric α-and β-relaxation of 1-propanol and o-terphenyl.
Hansen C, et al.
J. Chem. Phys., 107, 1086-1093 (1997)
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