Skip to Content
MilliporeSigma
All Photos(1)

Documents

L092003

Sigma-Aldrich

Ethyl acetate

Synonym(s):

EtOAc

Sign Into View Organizational & Contract Pricing
All Photos(1)

About This Item

Linear Formula:
CH3COOC2H5
CAS Number:
141-78-6
Molecular Weight:
88.11
Beilstein/REAXYS Number:
506104
EC Number:
205-500-4
MDL number:
MFCD00009171
UNSPSC Code:
12352200

vapor density

3 (20 °C, vs air)

Quality Level

200

vapor pressure

73 mmHg ( 20 °C)

form

liquid

autoignition temp.

801 °F

expl. lim.

2.2-11.5 %, 38 °F

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.)

format

neat

SMILES string

CCOC(C)=O

InChI

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

InChI key

XEKOWRVHYACXOJ-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

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_germany

WGK 1

flash_point_f

24.8 °F

flash_point_c

-4 °C

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Customers Also Viewed

Slide 1 of 6

1 of 6

Ethyl acetate ACS reagent, ≥99.5%

Sigma-Aldrich

319902

Ethyl acetate

Ethyl acetate analytical standard

Supelco

58958

Ethyl acetate

Ethyl acetate for liquid chromatography LiChrosolv®

Supelco

1.00868

Ethyl acetate

Ethyl acetate for analysis EMSURE® ACS,ISO,Reag. Ph Eur

Supelco

1.09623

Ethyl acetate

Ethyl acetate EMPROVE® ESSENTIAL, Ph. Eur., BP, NF

SAFC

1.00864

Ethyl acetate

Ethyl acetate ACS reagent, ≥99.5%

Sigma-Aldrich

676810

Ethyl acetate

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.
View All Related Papers

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service