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B85919

Sigma-Aldrich

2-Butanol

ReagentPlus®, ≥99%

Synonym(s):

sec-Butyl alcohol

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About This Item

Linear Formula:
CH3CH2CH(OH)CH3
CAS Number:
Molecular Weight:
74.12
Beilstein:
773649
EC Number:
MDL number:
UNSPSC Code:
12352001
PubChem Substance ID:
NACRES:
NA.21

vapor density

2.6 (vs air)

Quality Level

vapor pressure

12.5 mmHg ( 20 °C)

product line

ReagentPlus®

Assay

≥99%

form

liquid

autoignition temp.

761 °F

expl. lim.

9.8 %

IVD

for in vitro diagnostic use

refractive index

n20/D 1.397 (lit.)

bp

98 °C (lit.)

mp

−115 °C (lit.)

density

0.808 g/mL at 25 °C (lit.)

SMILES string

CCC(C)O

InChI

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

InChI key

BTANRVKWQNVYAZ-UHFFFAOYSA-N

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General description

2-Butanol is secondary alcohol mainly used as a solvent in organic synthesis. 2-butanol readily converts into 2-butanone (methyl ethyl ketone, MEK), which is used as a solvent in the industrial sector and many domestic cleaning products. It is an intermediate in devulcanizing rubber and the production of alkyl ester for use as biodiesel fuel.

Application

2-Butanol is used:
  • As a precursor to produce 2-butanone in presence of KMnO4 oxidant and CPC (N-cetylpyridinium chloride) micellar catalyst.
  • In the production of CH3NH3PbI3 perovskite films.

Legal Information

ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany

Pictograms

FlameExclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

Eye Irrit. 2 - Flam. Liq. 3 - STOT SE 3

Target Organs

Central nervous system, Respiratory system

Storage Class Code

3 - Flammable liquids

WGK

WGK 1

Flash Point(F)

80.6 °F - closed cup

Flash Point(C)

27 °C - closed cup


Certificates of Analysis (COA)

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Fengli Yang et al.
Chemical communications (Cambridge, England), 47(15), 4469-4471 (2011-03-04)
A new solid acid, based on tantalum hydroxide, was used to catalyze saccharide dehydration into 5-hydroxymethylfurfural (HMF) with high catalytic activity and excellent stability in a water-2-butanol biphasic system. Furthermore, good results were also obtained from Jerusalem artichoke juice with
Ravi K Pathak et al.
Environmental science & technology, 46(21), 11660-11669 (2012-09-19)
Limonene has a strong tendency to form secondary organic aerosol (SOA) in the atmosphere and in indoor environments. Initial oxidation occurs mainly via ozone or OH radical chemistry. We studied the effect of O(3) concentrations with or without a OH
Dagmara Wojtków et al.
The journal of physical chemistry. A, 110(36), 10552-10557 (2006-09-08)
The effect of temperature and concentration on the structure of sec-butyl alcohol and isobutyl alcohol/water binary mixtures in the alcohol-rich region (mole fraction of water X(H2O) < 0.3) has been studied using Fourier transform (FT) near-infrared (NIR) spectroscopy. The experimental
Mark B Shiflett et al.
The journal of physical chemistry. B, 110(29), 14436-14443 (2006-07-21)
In this article, we investigate vapor-liquid-liquid equilibria (VLLE) of binary systems using a simple volumetric method. Being different from the usual cloud-point method for the determination of liquid-liquid separation boundaries, the present volumetric method is able to determine the direct
Flaminia Rondino et al.
Physical chemistry chemical physics : PCCP, 13(3), 818-824 (2010-12-07)
Diastereomeric adducts between (S)-1-(4-fluorophenyl)-ethanol and R and S 2-butanol, formed by supersonic expansion, have been investigated by means of a combination of mass selected resonant two-photon ionization-spectroscopy and infrared depletion spectroscopy. Chiral recognition is evidenced by the specific spectroscopic signatures

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