Merck
All Photos(3)

279544

Sigma-Aldrich

1-Propanol

anhydrous, 99.7%

Synonym(s):
Propyl alcohol
Linear Formula:
CH3CH2CH2OH
CAS Number:
Molecular Weight:
60.10
Beilstein:
1098242
EC Number:
MDL number:
PubChem Substance ID:

Quality Level

grade

anhydrous

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.

Packaging

1, 2 L in Sure/Seal™
100 mL in Sure/Seal™

Signal Word

Danger

Hazard 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

Certificate of Analysis

Enter Lot Number to search for Certificate of Analysis (COA).

Certificate of Origin

Enter Lot Number to search for Certificate of Origin (COO).

Synthesis of unsymmetrical biaryls using a modified Suzuki cross-coupling: 4-biphenylcarboxaldehyde
Bret EH, et al.
Organic Syntheses, 75, 53-53 (1998)
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 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)
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