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About This Item
Linear Formula:
CH3CH2CH2OH
CAS Number:
Molecular Weight:
60.10
Beilstein:
1098242
EC Number:
MDL number:
UNSPSC Code:
12352001
PubChem Substance ID:
Grade:
anhydrous
Assay:
99.7%
Bp:
97 °C (lit.)
Vapor pressure:
10 mmHg ( 147 °C)
14.9 mmHg ( 20 °C)
14.9 mmHg ( 20 °C)
grade
anhydrous
Quality Level
vapor density
2.1 (vs air)
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)
bp
97 °C (lit.)
mp
−127 °C (lit.)
density
0.804 g/mL at 25 °C (lit.)
SMILES string
CCCO
InChI
1S/C3H8O/c1-2-3-4/h4H,2-3H2,1H3
InChI key
BDERNNFJNOPAEC-UHFFFAOYSA-N
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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.
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Dam. 1 - Flam. Liq. 2 - STOT SE 3
Target Organs
Central nervous system
Storage Class Code
3 - Flammable liquids
WGK
WGK 1
Flash Point(F)
71.6 °F - closed cup
Flash Point(C)
22 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
危险化学品
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Synthesis of 3-pentanone from 1-propanol over CeO2-Fe2O3 catalysts
Kamimura Y, et al
Applied Catalysis A: General, 252(2), 399-410 (2003)
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)
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