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Key Documents

779342

Sigma-Aldrich

Glycidyl methacrylate

≥97.0% (GC)

Synonym(s):

GMA, 2,3-Epoxypropyl methacrylate, Methacrylic acid 2,3-epoxypropyl ester

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100 μG
CN¥4,239.58

CN¥4,239.58


Estimated to ship onMay 06, 2025Details


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100 μG
CN¥4,239.58

About This Item

Empirical Formula (Hill Notation):
C7H10O3
CAS Number:
Molecular Weight:
142.15
Beilstein:
2506
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

CN¥4,239.58


Estimated to ship onMay 06, 2025Details


Request a Bulk Order

Assay

≥97.0% (GC)

form

liquid

contains

~0.01% hydrochinone monomethylether as stabilizer

refractive index

n20/D 1.449 (lit.)
n20/D 1.450

bp

189 °C (lit.)

density

1.075 g/mL at 20 °C
1.042 g/mL at 25 °C (lit.)

functional group

ester
ether
methacrylate

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

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1 of 4

This Item
15123814806789873
Quality Level

200

Quality Level

200

Quality Level

100

Quality Level

-

density

1.075 g/mL at 20 °C, 1.042 g/mL at 25 °C (lit.)

density

1.042 g/mL at 25 °C (lit.)

density

-

density

1.042 g/mL at 25 °C (lit.)

bp

189 °C (lit.)

bp

189 °C (lit.)

bp

-

bp

189 °C (lit.)

refractive index

n20/D 1.449 (lit.), n20/D 1.450

refractive index

n20/D 1.449 (lit.)

refractive index

-

refractive index

n20/D 1.447-1.451, n20/D 1.449 (lit.)

form

liquid

form

liquid

form

solid

form

liquid

Application

Glycidyl methacrylate (GMA) is an epoxy-functional monomer generally used to derivatize polymers.[1][2] It can also undergo polymerization to form poly (glycidyl methacrylate).[3]

Signal Word

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

Storage Class Code

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

WGK

WGK 3

Flash Point(F)

168.8 °F - closed cup

Flash Point(C)

76 °C - closed cup


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    Effect of glycidyl methacrylate (GMA) on the thermal, mechanical and morphological property of biodegradable PLA/PBAT blend and its nanocomposites.
    Kumar M, et al.
    Bioresource Technology, 101(21), 8406-8415 (2010)
    Biologically active polymers: synthesis and antimicrobial activity of modified glycidyl methacrylate polymers having a quaternary ammonium and phosphonium groups.
    Kenawy E-R, et al.
    Journal of Controlled Release : Official Journal of the Controlled Release Society, 50(1-2), 145-152 (1998)
    Synthesis, characterization, and polymerization of glycidyl methacrylate derivatized dextran.
    van Dijk-Wolthuis WNE, et al.
    Macromolecules, 28(18), 6317-6322 (1995)
    Adam Blanazs et al.
    Journal of the American Chemical Society, 133(41), 16581-16587 (2011-08-19)
    Amphiphilic diblock copolymers composed of two covalently linked, chemically distinct chains can be considered to be biological mimics of cell membrane-forming lipid molecules, but with typically more than an order of magnitude increase in molecular weight. These macromolecular amphiphiles are
    Liang Yuan et al.
    Biosensors & bioelectronics, 38(1), 79-85 (2012-07-07)
    A novel label-free immunosensing strategy for sensitive detection of tumor necrosis factor-alpha antigen (TNF-α) via surface-initiated atom transfer radical polymerization (SI-ATRP) was proposed. In this strategy, the Au electrode was first modified by consecutive SI-ATRP of ferrocenylmethyl methacrylate (FMMA) and

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