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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:
78-92-2
Molecular Weight:
74.12
Beilstein:
773649
EC Number:
201-158-5
MDL number:
MFCD00004569
UNSPSC Code:
12352001
PubChem Substance ID:
329773311
NACRES:
NA.21

vapor density

2.6 (vs air)

Quality Level

100

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
GHS02,GHS07

Signal Word

Warning

Hazard Statements

H226,H319,H335,H336

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)

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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Prabha Dwivedi et al.
Analytical chemistry, 78(24), 8200-8206 (2006-12-15)
This article introduces the concept of chiral ion mobility spectrometry (CIMS) and presents examples demonstrating the gas-phase separation of enantiomers of a wide range of racemates including pharmaceuticals, amino acids, and carbohydrates. CIMS is similar to traditional ion mobility spectrometry
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
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
Robert Brosnan et al.
Anesthesia and analgesia, 103(1), 86-91 (2006-06-23)
Chirality has been proposed as a means for distinguishing relevant from irrelevant molecular targets of action, but the sensitivity and specificity of this test is unknown for volatile anesthetics. We applied enantiomers of two chiral anesthetic alcohols (2-butanol and 2-pentanol)
Timothy E Morey et al.
AIDS and behavior, 17(1), 298-306 (2012-09-25)
A breath-based adherence system to document ingestion of oral medications (e.g., HAART) was investigated. Specifically, the food additive 2-butanol, which can be easily packaged with a drug, is converted via alcohol dehydrogenase to the volatile metabolite 2-butanone that rapidly appears
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