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Merck
CN

443468

2-丁酮

ACS reagent, ≥99.0%

别名:

MEK, 乙基甲基酮, 甲基乙基酮

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关于此项目

线性分子式:
C2H5COCH3
化学文摘社编号:
分子量:
72.11
EC Number:
201-159-0
UNSPSC Code:
12190000
MDL number:
Beilstein/REAXYS Number:
741880
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grade

ACS reagent

vapor density

2.49 (vs air)

vapor pressure

71 mmHg ( 20 °C)

assay

≥99.0%

autoignition temp.

960 °F

expl. lim.

10.1 %

impurities

≤0.0005 meq/g Titr. acid, ≤0.20% water

evapn. residue

≤0.0025%

color

APHA: ≤15

refractive index

n20/D 1.379 (lit.)

bp

80 °C (lit.)

mp

−87 °C (lit.)

density

0.805 g/mL at 25 °C (lit.)

SMILES string

CC(CC)=O

InChI

1S/C4H8O/c1-3-4(2)5/h3H2,1-2H3

InChI key

ZWEHNKRNPOVVGH-UHFFFAOYSA-N

General description

2-Butanone (Methyl ethyl ketone, MEK), an aliphatic ketone, is considered as aprotic and protophilic solvent. The solvent composition plays an important role in the rate of liquid-phase catalytic hydrogenation of MEK to 2-butanol. The rate constant for the reaction of hydroxyl radicals with MEK has been determined and expressed in Arrhenius form as ΚC2H5COCH3+OH = 6.35*1013 exp(-2270/T) cm3mol-1s-1.

Application

2-Butanone may be used as an oxidizing agent for the conversion of primary alcohols to the corresponding aldehydes via Oppenauer oxidation in the presence of an iridium complex.


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pictograms

FlameExclamation mark

signalword

Danger

Hazard Classifications

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

target_organs

Central nervous system

supp_hazards

存储类别

3 - Flammable liquids

wgk

WGK 1

flash_point_f

30.2 °F - closed cup

flash_point_c

-1 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

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分析证书(COA)

Lot/Batch Number

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High-Temperature Measurements of the Reactions of OH with a Series of Ketones: Acetone, 2-Butanone, 3-Pentanone, and 2-Pentanone.
Lam KY, et al.
The Journal of Physical Chemistry A, 116(23), 5549-5559 (2012)
Densities and viscosities of binary liquid mixtures of 2-butanone with branched alcohols at (293.15 to 313.15)K.
Lomte SB, et al.
Journal of Chemical and Engineering Data, 54(1), 127-130 (2008)
Iridium-catalyzed Oppenauer oxidations of primary alcohols using acetone or 2-butanone as oxidant.
Suzuki T, et al.
The Journal of Organic Chemistry, 68(4), 1601-1602 (2003)