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Sigma-Aldrich

2-Methyl-1-propanol

99.5%

Synonym(s):

Isobutanol, Isobutyl alcohol

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About This Item

Linear Formula:
(CH3)2CHCH2OH
CAS Number:
78-83-1
Molecular Weight:
74.12
Beilstein:
1730878
EC Number:
201-148-0
MDL number:
MFCD00004740
UNSPSC Code:
12352001
PubChem Substance ID:
329758003
NACRES:
NA.21

vapor density

2.55 (vs air)

vapor pressure

8 mmHg ( 20 °C)
8.8 mmHg ( 0 °C)

Assay

99.5%

form

liquid

autoignition temp.

801 °F

expl. lim.

10.6 %

impurities

≤0.05% (water)

refractive index

n20/D 1.396 (lit.)

bp

108 °C (lit.)

mp

−108 °C (lit.)

solubility

water: miscible 70 g/L at 20 °C

density

0.803 g/mL at 25 °C (lit.)

SMILES string

CC(C)CO

InChI

1S/C4H10O/c1-4(2)3-5/h4-5H,3H2,1-2H3

InChI key

ZXEKIIBDNHEJCQ-UHFFFAOYSA-N

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General description

2-Methyl-1-propanol, also known as isobutyl alcohol, is an aliphatic alcohol. The densities, viscosities and refractive indices of the binary mixtures of diglyme and 2-methyl-1-propanol have been evaluated. The partition functions and thermodynamic properties of 2-methyl-1-propanol in the vapor phase have been reported. The kinetics of dehydration of isobutyl alcohol to butene over ZSM (Zeolite Socony Mobil)-5 zeolite has been investigated using in situ FTIR (Fourier transform infrared spectroscopy) and GC. The thermochemical characteristics of radicals generated by the removal of hydrogen from 1-butanol have been studied.

Application

2-Methyl-1-propanol may be used in the synthesis of corresponding ester by reacting with acetic acid in the presence of a solid superacid.

Signal Word

Danger

Hazard Statements

H226,H315,H318,H335,H336

Hazard Classifications

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

Target Organs

Central nervous system, Respiratory system

Storage Class Code

3 - Flammable liquids

WGK

WGK 1

Flash Point(F)

82.4 °F - closed cup

Flash Point(C)

28 °C - closed cup

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Synthesis of Esters from Acetic Acid with Methanol, Ethanol, Propanol, Butanol, and Isobutyl Alcohol Catalyzed by Solid Superacid1.
Hino M and Arata K.
Chemistry Letters (Jpn), 10(12), 1671-1672 (1981)
Densities, viscosities, and refractive indices of the binary mixtures of bis(2-methoxyethyl)ether with 1-propanol, 1-butanol, 2-methyl-1-propanol, and 2-methyl-2-propanol.
Aminabhavi TM and Gopalkrishna B.
Journal of Chemical and Engineering Data, 39(4), 865-867 (1994)
Mechanistic studies of the catalytic dehydration of isobutyl alcohol on NaH-ZSM-5.
Williams C, et al.
J. Chem. Soc., Faraday Trans., 86(20), 3473-3485 (1990)
Jan-Karl Guterl et al.
ChemSusChem, 5(11), 2165-2172 (2012-10-23)
The limited supply of fossil resources demands the development of renewable alternatives to petroleum-based products. Here, biobased higher alcohols such as isobutanol are versatile platform molecules for the synthesis of chemical commodities and fuels. Currently, their fermentation-based production is limited
Antonino Baez et al.
Applied microbiology and biotechnology, 90(5), 1681-1690 (2011-05-07)
Promising approaches to produce higher alcohols, e.g., isobutanol, using Escherichia coli have been developed with successful results. Here, we translated the isobutanol process from shake flasks to a 1-L bioreactor in order to characterize three E. coli strains. With in
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