Key Documents

View All Documentation

Ethyl acetate

Name: Ethyl acetate
Brand: SIGMA

Synonym(s):

EtOAc

Select a Size

Change View

Pack Size	SKU	Availability	Price

About This Item

Linear Formula:

CH₃COOC₂H₅

CAS Number:

141-78-6

Molecular Weight:

88.11

EC Number:

205-500-4

UNSPSC Code:

12352108

MDL number:

MFCD00009171

Beilstein/REAXYS Number:

506104

NACRES:

NA.01

Bp:

76.5-77.5 °C (lit.)

Vapor pressure:

73 mmHg ( 20 °C)

Pricing and availability is not currently available.

Technical Service

Need help? Our team of experienced scientists is here for you.

Let Us Assist

Properties

vapor density

3 (20 °C, vs air)

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

Description

Compare Similar Items

View Full Comparison

Show Differences

1 of 1

This Item	1.09623	1.10972	1.00863
Sigma-Aldrich L092003 Ethyl acetate	Supelco 1.09623 Ethyl acetate	Supelco 1.10972 Ethyl acetate	Supelco 1.00863 Ethyl acetate
solubility water: soluble	solubility 85.3 g/L	solubility 85.3 g/L	solubility 85.3 g/L
form liquid	form liquid	form liquid	form liquid
autoignition temp. 801 °F	autoignition temp. 801 °F	autoignition temp. 801 °F	autoignition temp. 801 °F
density 0.902 g/mL at 25 °C (lit.)	density 0.902 g/mL at 25 °C (lit.)	density 0.902 g/mL at 25 °C (lit.)	density 0.902 g/mL at 25 °C (lit.)
vapor pressure 73 mmHg ( 20 °C)	vapor pressure 73 mmHg ( 20 °C)	vapor pressure 73 mmHg ( 20 °C)	vapor pressure 73 mmHg ( 20 °C)
expl. lim. 2.2-11.5 %, 38 °F	expl. lim. 2.2-11.5 %, 38 °F	expl. lim. 2.2-11.5 %, 38 °F	expl. lim. 2.2-11.5 %, 38 °F

Still not finding the right product?

Explore all of our products under Ethyl acetate

pictograms

GHS02,GHS07

signalword

Danger

hcodes

H225,H319,H336

pcodes

P210 - P233 - P240 - P241 - P242 - P305 + P351 + P338

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

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

It looks like we've run into a problem, but you can still download Certificates of Analysis from our Documents section.

If you need assistance, please contact Customer Support

Already Own This Product?

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

Visit the Document Library

Osmotic stress represses strigolactone biosynthesis in Lotus japonicus roots: exploring the interaction between strigolactones and ABA under abiotic stress.

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

In planta variation of volatile biosynthesis: an alternative biosynthetic route to the formation of the pathogen-induced volatile homoterpene DMNT via triterpene degradation in Arabidopsis roots.

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

Enzymatic oxidation of cholesterol: properties and functional effects of cholestenone in cell membranes.

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

View All Related Papers

Global Trade Item Number

SKU	GTIN
L092003-400L	04061838216441

Questions

Reviews

No rating value