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Merck
CN

16371

Ethyl acetate

Laboratory Reagent, ≥99.0% (GC)

Synonym(s):

EtOAc

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About This Item

Linear Formula:
CH3COOC2H5
CAS Number:
141-78-6
Molecular Weight:
88.11
EC Number:
205-500-4
UNSPSC Code:
12352108
PubChem Substance ID:
329751202
Beilstein/REAXYS Number:
506104
MDL number:
MFCD00009171

Key Documents

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InChI key

XEKOWRVHYACXOJ-UHFFFAOYSA-N

InChI

1S/C4H8O2/c1-3-6-4(2)5/h3H2,1-2H3

SMILES string

CCOC(C)=O

grade

Laboratory Reagent

vapor density

3 (20 °C, vs air)

vapor pressure

73 mmHg ( 20 °C)

assay

≥99.0% (GC)

autoignition temp.

801 °F

expl. lim.

2.2-11.5 %, 38 °F

impurities

≤0.003% acidity (as CH3COOH), ≤0.05% water

evapn. residue

≤0.003%

refractive index

n20/D 1.3720 (lit.)

mp

−84 °C (lit.)

density

0.902 g/mL at 25 °C (lit.)

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pictograms

FlameExclamation mark
GHS02,GHS07

signalword

Danger

Hazard Classifications

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

target_organs

Respiratory system

supp_hazards

EUH066

Storage Class

3 - Flammable liquids

wgk

WGK 1

flash_point_f

24.8 °F - closed cup

flash_point_c

-4 °C - closed cup

Regulatory Information

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Jeong-Hyeok Im et al.
Nanoscale, 3(10), 4088-4093 (2011-09-08)
Highly efficient quantum-dot-sensitized solar cell is fabricated using ca. 2-3 nm sized perovskite (CH(3)NH(3))PbI(3) nanocrystal. Spin-coating of the equimolar mixture of CH(3)NH(3)I and PbI(2) in γ-butyrolactone solution (perovskite precursor solution) leads to (CH(3)NH(3))PbI(3) quantum dots (QDs) on nanocrystalline TiO(2) surface.
C Pelletier et al.
Applied and environmental microbiology, 63(5), 1725-1731 (1997-05-01)
Hydrophilic and electrostatic cell surface properties of eight Lactobacillus strains were characterized by using the microbial adhesion to solvents method and microelectrophoresis, respectively. All strains appeared relatively hydrophilic. The strong microbial adhesion to chloroform, an acidic solvent, in comparison with
Complete oxidation of CO, ethanol, and ethyl acetate over copper oxide supported on titania and ceria modified titania.
Larsson PO and Andersson A.
J. Catal., 179(1), 72-89 (1998)
Mukesh Kumar Modi et al.
Bioresource technology, 98(6), 1260-1264 (2006-07-11)
Ethyl acetate was explored as an acyl acceptor for immobilized lipase-catalyzed preparation of biodiesel from the crude oils of Jatropha curcas (jatropha), Pongamia pinnata (karanj) and Helianthus annuus (sunflower). The optimum reaction conditions for interesterification of the oils with ethyl
K H Young et al.
Journal of clinical microbiology, 10(6), 852-853 (1979-12-01)
Ethyl acetate appears to be a satisfactory subsitute solvent for diethyl ether in the Formalin-ether sedimentation technique. In comparative studies, concentration of organisms with ethyl acetate was equal to or greater than that with diethyl ether. No distortion or alteration
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