POLY(ETHYLENE GLYCOL) METHYL ETHER ACRYLATE CAS#: 32171-39-4; ChemWhat Code: 51523

IdentificationPhysical DataSpectra
Route of Synthesis (ROS)Safety and HazardsOther Data

Identification

Product NamePOLY(ETHYLENE GLYCOL) METHYL ETHER ACRYLATE
IUPAC Name2-methoxyethyl prop-2-enoate 
Molecular StructureStructure of POLY(ETHYLENE GLYCOL) METHYL ETHER ACRYLATE CAS 32171-39-4
CAS Registry Number 32171-39-4
MDL NumberMFCD00803685
Synonyms2-METHOXYETHYL ACRYLATE
3121-61-7
Methoxyethyl acrylate
2-Propenoic acid, 2-methoxyethyl ester
Ethylene glycol methyl ether acrylate
Methyl cellosolve acrylate
Ethylene glycol monomethyl ether acrylate
2-Methoxyethanol, acrylate
Sipomer MCA
Acrylic acid, 2-methoxyethyl ester
Glycol monomethyl ether acrylate
Acrylic acid, 2-methoxyethoxy ester
Ethanol, 2-methoxy-, acrylate
2-Propenioc acid, 2-methoxyethyl ester
NSC 24153
Ageflex MEA
EINECS 221-499-3
BRN 1754333
AI3-15726
NSC-24153
515K4I683Y
DTXSID7025554
EC 221-499-3
METHOXYETHYL ACRYLATE, 2-
2-METHOXYETHYL 2-PROPENOATE
DTXCID605554
SR 244
Acrylic acid, 2-methoxyethyl ester (8CI)
221-499-3
2-methoxyethyl prop-2-enoate
32171-39-4
2-Methoxyethoxy acrylate
MFCD00803685
2-Methoxyethylacrylate
mPEG-Acrylate
Acryl-PEG
Methoxyethyl acrylate(13cp(25 degrees c))
MFCD00048149
UNII-515K4I683Y
Acrylic Acid 2-Methoxyethyl Ester
methoxyethylacrylate
mPEG-AC
2-methyoxyethyl acrylate
SCHEMBL38483
WLN: QVYU1&2O1
WLN: 1U1VO2O1
HFCUBKYHMMPGBY-UHFFFAOYSA-
NSC24153
AKOS005206914
CS-W011111
BS-42697
SY074897
Ethylene glycol methyl ether acrylate, 98%
NS00004274
2-Methoxyethyl Acrylate (stabilized with MEHQ)
E77141
F77854
2-Methoxyethyl Acrylate, (stabilized with MEHQ)
EN300-1718841
Q27260866
Ethylene Glycol Monomethyl Ether Acrylate (stabilized with MEHQ)
InChI=1/C6H10O3/c1-3-6(7)9-5-4-8-2/h3H,1,4-5H2,2H3
Ethylene glycol methyl ether acrylate, contains 50-100 ppm MEHQ as inhibitor, 98%ne, 3-amino-;β-Aminopyridine
462-08-8
Molecular FormulaC6H10O3 
Molecular Weight130.139 
InChIInChI=1S/C6H10O3/c1-3-6(7)9-5-4-8-2/h3H,1,4-5H2,2H3
InChI KeyHFCUBKYHMMPGBY-UHFFFAOYSA-N
SMILESCOCCOC(=O)C=C
Patent Information
Patent IDTitlePublication Date
CN117924192Conjugated olefin derivative as well as preparation method and application thereof2024
CN1140576392-aryl pentadienoic acid ester containing terminal olefin and synthesis method thereof2022
CN1135829463-aryl-5-thio-1,3,4-thiadiazole-2-thione derivative as well as preparation method and application thereof2021
CN110668942Alcohol-substituted (E, E)-configuration dendritic conjugated diene derivative and preparation method thereof2020
CN110642737Amide-substituted (E,E)-configuration dendritic conjugated diene derivative and preparation method thereof2020
CN110818630Synthesis method of conjugated (E)-3-cycloalkenyl acrylate derivative2020
CN110642752Alkenylation product of allylic alcohol carbamate compound and synthesis method thereof2020

Physical Data

AppearanceColorless transparent liquid
Boiling Point, °CPressure (Boiling Point), Torr
5612
Density, g·cm-3Reference Temperature, °CMeasurement Temperature, °C
1.0131420

Spectra

Description (IR Spectroscopy)
Spectrum

Route of Synthesis (ROS)

Route of POLY(ETHYLENE GLYCOL) METHYL ETHER ACRYLATE CAS 32171-39-4
Route of POLY(ETHYLENE GLYCOL) METHYL ETHER ACRYLATE CAS 32171-39-4
ConditionsYield
With tetrabutoxytitanium; 4-methoxy-phenol In o-xylene at 80 – 90℃; under 75.0075 Torr;

Experimental Procedure
In a 500 ml four-necked flask equipped with a distillation apparatus, a thermometer, and a stirrer,1,4-butanediol monoglycidyl ether (hereinafter referred to as “14 BDMGE”100.0 g (purity: 93.7%, 0.64 mol in terms of purity)),125.1 g (0.96 mol) of 2-methoxyethyl acrylate,200.0 g of o-xylene and 0.03 g of MEHQ were added to prepare a raw material mixture solution(Total 425.1 g) were prepared.When the moisture content of this raw material mixture liquid was measured with a Karl Fischer moisture meter, it was 503 ppm, and the total amount of moisture contained was 0.21 g (0.012 mol). To the above raw material mixture solution, 4.4 g (0.013 mol) of TBT was added,While heating the solution under reduced pressure while reducing the pressure to 100 hPa, transesterification reaction was carried out at a reaction solution temperature of 80 to 90 ° C. while o-xylene and produced 2-methoxyethanol were distilled out of the reaction system.The temperature of the distillation gas was 57 to 74 ° C.Finally, 169.9 g of the fraction was withdrawn in 6 hours and the reaction was terminated to obtain 255.2 g of a reaction solution containing 4 HBAGE (46.3 wt%).The purity-converted quantitative yield of 4 HBAGE is 92.0%, and the molar ratio of the total amount of moisture in this reaction system is 0.9 times the TBT used. To the above reaction solution, 140.0 g of water was added, heated to 60 ° C. under normal pressure with stirring, and heated and hydrolyzed at 60 ° C. for 1 hour as it was. The reaction solution was cooled and suction filtered using a filter equipped with Celite to remove insoluble catalyst. The filtrate was separated into an organic layer and an aqueous layer. The organic layer containing 4 HBAGE was concentrated under reduced pressure using a rotary evaporator to obtain 130.8 g of 4 HBAGE crude product (purity 94.0%). The purity-converted quantitative yield of 4 HBAGE was 95.8%, and the content of titanium derived from TBT used as a catalyst was 2 ppm or less.50.0 g of the above 4 HBAGE crude product (130.8 g) was fractionated, 0.08 g of CBC was added thereto, and purification was carried out by simple distillation under reduced pressure. As a result, high purity 4 HBAGE (purity 96.9%) was obtained.The purity-converted quantitative yield of 4 HBAGE is 83.7% in terms of the consistent yield from the transesterification reaction. Conditions at the time of fractional distillation were 0.4 to 0.6 hPa in the degree of vacuum, 103 to 114 ° C. in the bottom liquid temperature, 93 to 95 ° C. in the distillation gas temperature, about 1 hour in distillation time there were. No polymer was observed in the distillation residue and in the distillation system.
83.7%

Safety and Hazards

Pictogram(s)flamecorrosionskullhealth-hazard
SignalDanger
GHS Hazard StatementsH226 (89.4%): Flammable liquid and vapor [Warning Flammable liquids]
H302 (89.4%): Harmful if swallowed [Warning Acute toxicity, oral]
H311+H331 (73.1%): Toxic in contact with skin or if inhaled. [Danger Acute toxicity, dermal; acute toxicity, inhalation]
H311 (89.4%): Toxic in contact with skin [Danger Acute toxicity, dermal]
H314 (74%): Causes severe skin burns and eye damage [Danger Skin corrosion/irritation]
H315 (25%): Causes skin irritation [Warning Skin corrosion/irritation]
H317 (77.9%): May cause an allergic skin reaction [Warning Sensitization, Skin]
H318 (37.5%): Causes serious eye damage [Danger Serious eye damage/eye irritation]
H319 (25%): Causes serious eye irritation [Warning Serious eye damage/eye irritation]
H331 (78.8%): Toxic if inhaled [Danger Acute toxicity, inhalation]
H332 (10.6%): Harmful if inhaled [Warning Acute toxicity, inhalation]
H335 (11.5%): May cause respiratory irritation [Warning Specific target organ toxicity, single exposure; Respiratory tract irritation]
H341 (19.2%): Suspected of causing genetic defects [Warning Germ cell mutagenicity]
H360 (57.7%): May damage fertility or the unborn child [Danger Reproductive toxicity]
H360FD (17.3%): May damage fertility; May damage the unborn child [Danger Reproductive toxicity]
H373 (63.5%): May causes damage to organs through prolonged or repeated exposure [Warning Specific target organ toxicity, repeated exposure]
H411 (15.4%): Toxic to aquatic life with long lasting effects [Hazardous to the aquatic environment, long-term hazard]
H412 (72.1%): Harmful to aquatic life with long lasting effects [Hazardous to the aquatic environment, long-term hazard]
Precautionary Statement CodesP203, P210, P233, P240, P241, P242, P243, P260, P261, P262, P264, P264+P265, P270, P271, P272, P273, P280, P301+P317, P301+P330+P331, P302+P352, P302+P361+P354, P303+P361+P353, P304+P340, P305+P351+P338, P305+P354+P338, P316, P317, P318, P319, P321, P330, P332+P317, P333+P317, P337+P317, P361+P364, P362+P364, P363, P370+P378, P391, P403+P233, P403+P235, P405, and P501
(The corresponding statement to each P-code can be found at the GHS Classification page.)

Other Data

TransportationStore at room temperature for long time, sealed and keep in a dry place.
HS Code
StorageStore at room temperature for long time, sealed and keep in a dry place.
Shelf Life1 year
Market Price
Druglikeness
Lipinski rules component
Molecular Weight130.144
logP-0.343
HBA3
HBD0
Matching Lipinski Rules4
Veber rules component
Polar Surface Area (PSA)35.53
Rotatable Bond (RotB)5
Matching Veber Rules2
Use Pattern
MPEG-AC CAS 32171-39-4 finds extensive applications in UV-curable systems and related fields. It is widely used as a key raw material in high-performance UV-curable adhesives, particularly for laminated glass, flexible displays, and optical device bonding. In UV-curable systems, it acts as a modifier to adjust curing speed, flexibility, and adhesion performance, optimizing the physical and chemical properties of the final product. It serves as a monomer in polymerization reactions for the synthesis of specialty acrylic resins or cyclohexyl-based compounds.

Buy Reagent

No reagent supplier? Send quick inquiry to ChemWhat
Want to be listed here as a reagent supplier? (Paid service) Click here to contact ChemWhat

Approved Manufacturers

Warshel Chemical Ltdhttps://www.warshel.com/
Want to be listed as an approved manufacturer (Requires approvement)? Please download and fill out this form and send back to approved-manufacturers@chemwhat.com

Contact Us for Other Help

Contact us for other information or services Click here to contact ChemWhat