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Merck
모든 사진(1)

문서

290815

Sigma-Aldrich

2-Ethylhexyl acrylate

98%, contains ≥0.001-≤0.11% monomethyl ether hydroquinone as stabilizer

동의어(들):

(±)-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
MDL number:
UNSPSC 코드:
12162002
PubChem Substance ID:
NACRES:
NA.23

vapor density

6.4 (vs air)

vapor pressure

0.15 mmHg ( 20 °C)

분석

98%

autoignition temp.

496 °F

포함

≥0.001-≤0.11% monomethyl ether hydroquinone as stabilizer

expl. lim.

6.4 %

refractive index

n20/D 1.436 (lit.)

bp

215-219 °C (lit.)

density

0.885 g/mL at 25 °C (lit.)

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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일반 설명

2-Ethylhexyl acrylate can undergo free radical solution polymerization to yield its polymer. It can form a series of copolymers via atom transfer radical copolymerization. A study reports the emulsion terpolymerization of the product with styrene, methacrylic acid.
2-ethylhexyl acrylate (EHA) is one of the constituents of acrylic polymeric latex. It can undergo free-radical solution polymerization. EHA is known to undergo free radical emulsion co- polymerization with methyl methacrylate (MMA) to form pressure-sensitive adhesives. It may also form copolymers with acrylonitrile and acrylamide.

애플리케이션

  • Formulation optimization and stability study of transdermal therapeutic system of nicorandil.: This research explores the formulation and stability of a transdermal therapeutic system using 2-ethylhexyl acrylate (2-EHA) as a key component, highlighting its potential in delivering drugs through the skin effectively (Tipre DN et al., 2002).

픽토그램

Exclamation mark

신호어

Warning

유해 및 위험 성명서

Hazard Classifications

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

표적 기관

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

개인 보호 장비

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter


시험 성적서(COA)

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문서 라이브러리 방문

Block, blocky gradient and random copolymers of 2-ethylhexyl acrylate and acrylic acid by atom transfer radical polymerization,
Vidts KRM, et al.
Polymer, 47(17), 6028-6037 (2006)
Design of pressure-sensitive adhesives by free-radical emulsion copolymerization of methyl methacrylate and 2-ethylhexyl acrylate. 1. Kinetic study and tack properties.
Aymonier A, et al.
Chemistry of Materials, 13(8), 2562-2566 (2001)
Synthesis and characterization of homopolymer of 2?ethylhexyl acrylate and its copolymers with acrylamide, acrylonitrile, and methyl methacrylate.
Vangani V and Rakshit AK
Journal of Applied Polymer Science, 60(7), 1005-1013 (1996)
Two dimensional chromatographic characterization of block copolymers of 2-ethylhexyl acrylate and methyl acrylate, P2EHA-b-PMA, produced via RAFT-mediated polymerization in organic dispersion.
Raust Jacques-Antoine et al.
Macromolecules, 43(21), 8755-8765 (2010)
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

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