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8.00609

2,3-Epoxypropyl methacrylate

Technipur®

Synonym(s):

Glycidyl methacrylate, 2-((Methacryloxy)methyl)oxirane, 2,3-Epoxypropyl methacrylate, Methacrylic acid 2,3-epoxypropyl ester

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Size/SKUAvailabilityPrice
250 mL
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$51.40
2.5 L
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$186.00
25 kg
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$1,230.00
200 kg
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$9,330.00

About This Item

Empirical Formula (Hill Notation):
C7H10O3
CAS Number:
Molecular Weight:
142.15
NACRES:
NA.21
UNSPSC Code:
12162002
Beilstein/REAXYS Number:
2506
MDL number:

$51.40


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grade

synthesis grade

Quality Segment

vapor pressure

4.2 hPa ( 25 °C)

refractive index

n20/D 1.449 (lit.)

bp

189 °C (lit.)

mp

<-60 °C

density

1.042 g/mL at 25 °C (lit.), 1.07 g/cm3 at 25 °C

SMILES string

CC(=C)C(=O)OCC1CO1

InChI

1S/C7H10O3/c1-5(2)7(8)10-4-6-3-9-6/h6H,1,3-4H2,2H3

InChI key

VOZRXNHHFUQHIL-UHFFFAOYSA-N

General description

2,3-Epoxypropyl methacrylate is a methacrylic acid/glycidol ester. It is used as a monomer to produce polymers based on glycidyl methacrylate (GMA). It is also a dual functionality (epoxy and methacrylate) monomer, thus offering the opportunity for chemical modification of the parent polymer for various applications.

Application

2,3-Epoxypropyl methacrylate can be used as a monomer unit in polymer industries to produce poly (glycidyl methacrylate)(PGMA) for various uses in electronic and biomedical applications. The presence of epoxide group in PGMA allows it to be modified by a variety of functionalities such as amine-epoxy, thiol-epoxy, azide-epoxy, and acid-epoxy via nucleophilic ring-opening reactions. This overall flexibility in the functionalization of PGMA is because of the controlled polymerization of 2,3-epoxypropyl methacrylate monomer via free radical polymerization. Thus, PGMA is one of the most adaptable reactive scaffolds in polymer chemistry due to the long shelf life of the resulting polymers.

It is also used to prepare poly(n-butyl methacrylate-co-glycidyl methacrylate) copolymers, which find applications in adhesives, surface coatings, and electrical devices in various polymeric industries. The presence of epoxy groups and flexible butyl groups in epoxy resin-modified copolymers increases its mechanical properties, impact strength, and fracture elongation.

Legal Information

Technipur is a registered trademark of Merck KGaA, Darmstadt, Germany

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This Item
8.005798.0059003558
grade

synthesis grade

grade

-

grade

-

grade

analytical standard

density

1.042 g/mL at 25 °C (lit.), 1.07 g/cm3 at 25 °C

density

0.913 g/cm3 at 20 °C

density

0.94 g/cm3 at 20 °C

density

1.200 g/cm3

mp

<-60 °C

mp

-61--59 °C

mp

-48 °C

mp

-

refractive index

n20/D 1.449 (lit.)

refractive index

-

refractive index

-

refractive index

-

bp

189 °C (lit.)

bp

119-121 °C/1013 hPa

bp

101 °C/1013 hPa

bp

-

vapor pressure

4.2 hPa ( 25 °C)

vapor pressure

21.3 hPa ( 20 °C)

vapor pressure

53 hPa ( 20 °C)

vapor pressure

-


signalword

Danger

Hazard Classifications

Acute Tox. 3 Dermal - Acute Tox. 4 Oral - Carc. 1B - Eye Dam. 1 - Muta. 2 - Repr. 1B - Skin Corr. 1C - Skin Sens. 1 - STOT RE 1 - STOT SE 3

target_organs

Respiratory system

wgk

WGK 3

flash_point_f

168.8 °F - closed cup

flash_point_c

76 °C - closed cup

Storage Class

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects



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