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Merck

676926

2-Butanone

ACS reagent, ≥99.0%

Synonyme(s) :

MEK, Méthyl éthyl cétone, Méthyléthylcétone

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A propos de cet article

Formule linéaire :
C2H5COCH3
Numéro CAS:
Poids moléculaire :
72.11
NACRES:
NA.21
PubChem Substance ID:
eCl@ss:
39021202
UNSPSC Code:
12352115
EC Number:
201-159-0
MDL number:
Beilstein/REAXYS Number:
741880
Assay:
≥99.0%
Grade:
ACS reagent
Bp:
80 °C (lit.)
Vapor pressure:
71 mmHg ( 20 °C)
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InChI key

ZWEHNKRNPOVVGH-UHFFFAOYSA-N

InChI

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

SMILES string

CC(CC)=O

grade

ACS reagent

vapor density

2.49 (vs air)

vapor pressure

71 mmHg ( 20 °C)

assay

≥99.0%

form

liquid

autoignition temp.

960 °F

expl. lim.

10.1 %

dilution

(for analytical testing)

impurities

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

evapn. residue

≤0.0025%

color

APHA: ≤15

Quality Level

refractive index

n20/D 1.379 (lit.)

bp

80 °C (lit.)

mp

−87 °C (lit.)

density

0.805 g/mL at 25 °C (lit.)

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General description

2-Butanone is a ketone. Physical properties of the solutions of 1-n-butyl-3-methylimidazolium tetrafluoroborate (ionic liquid) in various organic solvents (acetonitrile, dichloromethane, 2-butanone and N,N-dimethylformamide) has been studied. Viscosity and density of these mixtures were evaluated at 298.15K.
Our premium ACS solvents are ideal for routine chemical synthesis, drying, purification, and critical labware cleaning. They meet or exceed the rigorous standards of the American Chemical Society (ACS), ensuring high-quality results for your research needs.

Premium ACS Solvents: Our solvents meet or exceed the stringent standards set by the American Chemical Society, ensuring high quality and reliability for your laboratory applications.

Replicable and Publishable Results: Designed for consistency, our solvents deliver results that can be reliably reproduced, making them ideal for research that requires publication.

Versatile Applications: Suitable for routine chemical synthesis, drying, purification, and critical labware cleaning, our solvents cater to a wide range of research needs in the laboratory.

Application

2-Butanone (Methyl ethyl ketone) may be employed as solvent for the methylation agent [11C]methyl trifluoromethanesulfonate ([11C]CH3OTf), during the completely automated radiosynthesis of 2-(4-N-[11C]methylaminophenyl)-6-hydroxybenzothiazole ([11C]PIB). It may be used in the synthesis of nanocontainer composed of 6 bowl-shaped cavitands. In the nanocontainer, cavitands were joined by 12 -CH=N-CH2CH2-N=CH- linkers.

pictograms

FlameExclamation mark

signalword

Danger

Hazard Classifications

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

target_organs

Central nervous system

supp_hazards

Classe de stockage

3 - Flammable liquids

wgk

WGK 1

flash_point_f

30.2 °F - closed cup

flash_point_c

-1 °C - closed cup


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Consulter la Bibliothèque de documents

A volumetric and viscosity study for the mixtures of 1-n-butyl-3-methylimidazolium tetrafluoroborate ionic liquid with acetonitrile, dichloromethane, 2-butanone and N, N-dimethylformamide.
Wang J, et al.
Green Chemistry, 5(5), 618-622 (2003)
A simple one-pot multicomponent synthesis of an octahedral nanocontainer molecule.
Liu X and Warmuth R.
Nature Protocols, 2(5), 1288-1296 (2007)
C Philippe et al.
Applied radiation and isotopes : including data, instrumentation and methods for use in agriculture, industry and medicine, 69(9), 1212-1217 (2011-05-10)
[(11)C]PIB is still the standard PET compound for Alzheimer imaging targeting beta-amyloid plaques. We aimed to establish a fully-automated procedure for the synthesis and purification of [(11)C]PIB with a high degree of reliability and improved specific activity as well as
S G Carmella et al.
Cancer research, 53(4), 721-724 (1993-02-15)
Metabolites of the tobacco-specific nitrosamine, 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone, a potent pulmonary carcinogen, have been quantified in the urine of 11 smokers. They were not detected in nonsmokers' urine. The metabolites, 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanol and its glucuronide, were detected in quantities of 0.23-1.0 and 0.57-6.5
L B Goldsmith et al.
Contact dermatitis, 19(5), 348-350 (1988-11-01)
Irritant contact dermatitis along with an increased transepidermal water loss can result from exposing the skin to solvents. A study of the interaction of various solvents with human stratum corneum was made using thin-layer chromatography. Comparison of 10 solvents (trichloroethylene

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