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34871

Sigma-Aldrich

1-Propanol

suitable for HPLC, ≥99.9%

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Synonym(s):
Propyl alcohol
Linear Formula:
CH3CH2CH2OH
CAS Number:
Molecular Weight:
60.10
Beilstein/REAXYS Number:
1098242
EC Number:
MDL number:
PubChem Substance ID:
NACRES:
NA.05

vapor density

2.1 (vs air)

Quality Level

vapor pressure

10 mmHg ( 147 °C)
14.9 mmHg ( 20 °C)

assay

≥99.9%

form

liquid

autoignition temp.

700 °F

expl. lim.

13.7 %

technique(s)

HPLC: suitable

impurities

≤0.0005% non-volatile matter
≤0.001% free acid (as C2H5COOH)
≤0.05% water (Karl Fischer)

evapn. residue

≤0.005%

transmittance

220 nm, ≥40%
240 nm, ≥85%
275 nm, ≥99%

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.)

λ

neat

UV absorption

λ: 220 nm Amax: ≤0.40
λ: 240 nm Amax: ≤0.071
λ: 275 nm Amax: ≤0.0044

SMILES string

CCCO

InChI

1S/C3H8O/c1-2-3-4/h4H,2-3H2,1H3

InChI key

BDERNNFJNOPAEC-UHFFFAOYSA-N

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1 of 4

This Item
402893965661.01024
vibrant-m

34871

1-Propanol

vibrant-m

402893

1-Propanol

vibrant-m

96566

1-Propanol

vibrant-m

1.01024

1-Propanol

assay

≥99.9%

assay

≥99.5%

assay

≥99.9% (GC)

assay

≥99.8% (GC)

technique(s)

HPLC: suitable

technique(s)

-

technique(s)

HPLC: suitable, gas chromatography (GC): suitable

technique(s)

HPLC: suitable

form

liquid

form

liquid

form

-

form

liquid

refractive index

n20/D 1.384 (lit.)

refractive index

n20/D 1.384 (lit.)

refractive index

n20/D 1.384 (lit.), n20/D 1.385

refractive index

-

impurities

≤0.0005% non-volatile matter, ≤0.05% water (Karl Fischer), ≤0.001% free acid (as C2H5COOH)

impurities

≤0.0004 meq/g Titr. acid, ≤0.01% ethanol, ≤0.01% methanol, ≤0.03% Carbonyl compounds (as C2H5CHO), ≤0.05% CH3CHOHCH3, ≤0.05% isopropanol, ≤0.2% water

impurities

-

impurities

≤0.0002 meq/g Acidity, ≤0.0002 meq/g Alkalinity, ≤0.02% Water

General description

1-Propanol is a linear alcohol. It exhibits Debye-type relaxation process which ressembles the α-relaxation and Johari-Goldstein type β-relaxation features of the supercooled liquids (nonhydrogen-bonding type). It has been tested as a substitute of the fuel for various fuel cells. Its biosynthesis from glucose using Escherichia coli strain has been proposed.

Application

1-Propanol may be employed as a solvent for the synthesis of mesoporous alumina.

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signalword

Danger

Hazard Classifications

Eye Dam. 1 - Flam. Liq. 2 - STOT SE 3

target_organs

Central nervous system

Storage Class

3 - Flammable liquids

wgk_germany

WGK 1

flash_point_f

71.6 °F - closed cup

flash_point_c

22 °C - closed cup


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1-Propanol United States Pharmacopeia (USP) Reference Standard

USP

1570406

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1-Propanol natural, ≥98%, FG

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2-Propanol suitable for HPLC, 99.9%

Sigma-Aldrich

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Juan Antonio Cecilia et al.
Materials (Basel, Switzerland), 11(9) (2018-09-12)
Vanadium oxide (V₂O₅) species has been supported on different porous clay heterostructures (with silica pillars, silica-zirconia with a molar ratio Si/Zr = 5 and silica-titania with a molar ratio Si/Ti = 5) by wetness incipient method. All catalysts were characterized
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)
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)
Evaluation of Ethanol, 1-Propanol, and 2-Propanol in a Direct Oxidation Polymer-Electrolyte Fuel Cell A Real-Time Mass Spectrometry Study.
Wang J, et al.
Journal of the Electrochemical Society, 142(12), Wang J-Wang J (1995)
David Fernandez Rivas et al.
Ultrasonics sonochemistry, 19(6), 1252-1259 (2012-05-23)
Micromachined pits on a substrate can be used to nucleate and stabilize microbubbles in a liquid exposed to an ultrasonic field. Under suitable conditions, the collapse of these bubbles can result in light emission (sonoluminescence, SL). Hydroxyl radicals (OH()) generated

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