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2-Ethylhexyl acrylate

analytical standard

Synonym(s):

(±)-Acrylic acid 2-ethylhexyl ester

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About This Item

Linear Formula:
CH2=CHCOOCH2CH(C2H5)(CH2)3CH3
CAS Number:
Molecular Weight:
184.28
Beilstein:
1765828
EC Number:
MDL number:
UNSPSC Code:
41116107
PubChem Substance ID:
NACRES:
NA.24

grade

analytical standard

Quality Level

vapor density

6.4 (vs air)

vapor pressure

0.15 mmHg ( 20 °C)

Assay

≥99.5% (GC)

autoignition temp.

496 °F

shelf life

limited shelf life, expiry date on the label

contains

0.001-0.11% monomethyl ether hydroquinone as stabilizer

expl. lim.

6.4 %

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

refractive index

n20/D 1.436 (lit.)
n20/D 1.436

bp

215-219 °C (lit.)

density

0.884 g/mL at 20 °C
0.885 g/mL at 25 °C (lit.)

application(s)

cleaning products
cosmetics
environmental
food and beverages
personal care

format

neat

SMILES string

CCCCC(CC)COC(=O)C=C

InChI

1S/C11H20O2/c1-4-7-8-10(5-2)9-13-11(12)6-3/h6,10H,3-5,7-9H2,1-2H3

InChI key

GOXQRTZXKQZDDN-UHFFFAOYSA-N

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General description

2-Ethylhexyl acrylates are classified under the ester group of compounds.
This substance is listed on the positive list of the EU regulation 10/2011 for plastics intended to come into contact with food.

Find all available reference materials for compounds listed in 10/2011 here

Application

2-Ethylhexyl acrylate has been used as a reference standard for the analysis of 2-ethylhexyl acrylate in glossy water-based lacquer by thermal desorption and gas chromatography-mass spectrometry (GC-MS).
It may be used as a reference standard for the determination of 2-ethylhexyl acrylate in:
  • Exhaled breath samples from cigarette smokers by capillary micro-extracton (CMV) coupled with GC-MS.
  • Food paper contact papers by modified quick, easy, cheap, effective, rugged and safe (QuEchERS) extraction procedure combined with gas chromatography-tandem mass spectrometry (GC-MS/MS).
  • Polymer emulsions by headspace (HS) GC-MS operating on selected ion monitoring (SIM) mode.
  • Adhesives employed in food contact materials by ultra-performance liquid chromatography-quadrupole time-of-flight mass spectrometry (UPLC-QTOF/MS).

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

Aquatic Chronic 3 - Skin Irrit. 2 - Skin Sens. 1 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

10 - Combustible liquids

WGK

WGK 1

Flash Point(F)

174.2 °F - closed cup

Flash Point(C)

79 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Application of a novel reference material in an international round robin test on material emissions testing.
Horn W, et al.
Indoor Air, 28(1), 181-187 (2018)
Simultaneous determination of seven acrylates in food contact paper products by GC/MS and modified QuEChERS.
Xun Z, et al.
Analytical Methods : Advancing Methods and Applications, 8(19), 3953-3958 (2016)
R Peters et al.
Journal of chromatography. A, 1156(1-2), 111-123 (2006-11-23)
UV-cured networks prepared from mixtures of di-functional (polyethylene-glycol di-acrylate) and mono-functional (2-ethylhexyl acrylate) acrylates were analysed after hydrolysis, by aqueous size-exclusion chromatography coupled to on-line reversed-phase liquid-chromatography. The mean network density and the fraction of dangling chain ends of these
A H Shojaei et al.
Journal of controlled release : official journal of the Controlled Release Society, 67(2-3), 223-232 (2000-05-29)
Based on the premise that similar surface properties between the adhesive and the substrate would yield a strong adhesive bond, copolymers of acrylic acid (AA) and 2-ethylhexyl acrylate (EHA), P(AA-co-EHA), were designed and synthesized for buccal mucoadhesion. A series of
Dhruba J Haloi et al.
ACS applied materials & interfaces, 4(8), 4200-4207 (2012-07-28)
Acrylic block copolymers have several advantages over conventional styrenic block copolymers, because of the presence of a saturated backbone and polar pendant groups. This investigation reports the preparation and characterization of di- and triblock copolymers (AB and ABA types) of

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