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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
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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.)

SMILES string

CCOC(C)=O

InChI

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

InChI key

XEKOWRVHYACXOJ-UHFFFAOYSA-N

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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

Regulatory Information

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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
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