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Merck
CN

L090000-HH

Ethyl Acetate

Synonym(s):

Ethyl acetate, 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:
12352200
PubChem Substance ID:
329817378
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

vapor density

3 (20 °C, vs air)

vapor pressure

73 mmHg ( 20 °C)

product line

Proligo Reagents

assay

≥99.8% (GC)

autoignition temp.

801 °F

expl. lim.

2.2-11.5 %, 38 °F

packaging

pkg of 1 × 200 L L0920000-C03-01, pkg of 4 × 4 L L090400-04, pkg of 1 × 45 L L094500-01

impurities

≤0.02% Ethanol content (GC), ≤10 ppm Free acid (as acetic acid), ≤30 ppm water content (Karl Fischer)

color

clearAPHA: ≤10, Hazen

refractive index

n20/D 1.3720 (lit.)

bp

76.5-77.5 °C (lit.)

mp

−84 °C (lit.)

solubility

water: soluble

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

Central nervous 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

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Junwei Liu et al.
Planta, 241(6), 1435-1451 (2015-02-27)
Strigolactone changes and cross talk with ABA unveil a picture of root-specific hormonal dynamics under stress. Strigolactones (SLs) are carotenoid-derived hormones influencing diverse aspects of development and communication with (micro)organisms, and proposed as mediators of environmental stimuli in resource allocation
Reza Sohrabi et al.
The Plant cell, 27(3), 874-890 (2015-03-01)
Plant-derived volatile compounds such as terpenes exhibit substantial structural variation and serve multiple ecological functions. Despite their structural diversity, volatile terpenes are generally produced from a small number of core 5- to 20-carbon intermediates. Here, we present unexpected plasticity in
Tsukasa Horiyama et al.
PloS one, 9(9), e108642-e108642 (2014-09-27)
Escherichia coli produces the iron-chelating compound enterobactin to enable growth under iron-limiting conditions. After biosynthesis, enterobactin is released from the cell. However, the enterobactin export system is not fully understood. Previous studies have suggested that the outer membrane channel TolC
Maarit Neuvonen et al.
PloS one, 9(8), e103743-e103743 (2014-08-27)
Bacterial cholesterol oxidase is commonly used as an experimental tool to reduce cellular cholesterol content. That the treatment also generates the poorly degradable metabolite 4-cholesten-3-one (cholestenone) has received less attention. Here, we investigated the membrane partitioning of cholestenone using simulations
Angela Schwarm et al.
Archives of animal nutrition, 69(3), 159-176 (2015-05-13)
The aim of the present experiment was to compare silage prepared from maize having a brown midrib (BMR) mutation with control (CTR) maize to identify their effects on enteric methane emission, digesta mean retention time (MRT), ruminal fermentation and digestibility.
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