Sigma-Aldrich 290815 2-Ethylhexyl acrylate 98%, contains ≥0.001-≤0.11% monomethyl ether hydroquinone as stabilizer 1 L
Marka
Stok Kodu
LB.SA.290815-1L
Kısa Bilgi
Synonym(s): (±)-Acrylic acid 2-ethylhexyl ester Linear Formula: CH2=CHCOOCH2CH(C2H5)(CH2)3CH3 CAS Number: 103-11-7 Molecular Weight: 184.28 Beilstein: 1765828 MDL number: MFCD00009495 UNSPSC Code: 12162002 PubChem Substance ID: 24857489 NACRES: NA.23
Bilgi
CAS Number: 103-11-7
| Sigma-Aldrich 290815 2-Ethylhexyl acrylate 98%, contains ≥0.001-≤0.11% monomethyl ether hydroquinone as stabilizer |
| Synonym(s): (±)-Acrylic acid 2-ethylhexyl ester Linear Formula: CH2=CHCOOCH2CH(C2H5)(CH2)3CH3 CAS Number: 103-11-7 Molecular Weight: 184.28 Beilstein: 1765828 MDL number: MFCD00009495 UNSPSC Code: 12162002 PubChem Substance ID: 24857489 NACRES: NA.23 |
|
PROPERTIES
vapor density 6.4 (vs air)
vapor pressure 0.15 mmHg ( 20 °C) Assay 98% autoignition temp. 496 °F contains ≥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 DESCRIPTION General description 2-Ethylhexyl acrylate can undergo free radical solution polymerization to yield its polymer. [1] It can form a series of copolymers via atom transfer radical copolymerization. [2] A study reports the emulsion terpolymerization of the product with styrene, methacrylic acid. [3] 2-ethylhexyl acrylate (EHA) is one of the constituents of acrylic polymeric latex. [4]It can undergo free-radical solution polymerization.[1] EHA is known to undergo free radical emulsion co- polymerization with methyl methacrylate (MMA) to form pressure-sensitive adhesives. [5][6] It may also form copolymers with acrylonitrile and acrylamide. [7] Application 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). |
