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109606

Sigma-Aldrich

Methacrylamide

98%

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Synonym(s):
2-Methylacrylamide, 2-Methylpropenamide, Methacrylic acid amide
Linear Formula:
H2C=C(CH3)CONH2
CAS Number:
Molecular Weight:
85.10
Beilstein/REAXYS Number:
605397
EC Number:
MDL number:
PubChem Substance ID:
NACRES:
NA.23

Quality Level

assay

98%

form

solid

mp

106-110 °C (lit.)

SMILES string

CC(=C)C(N)=O

InChI

1S/C4H7NO/c1-3(2)4(5)6/h1H2,2H3,(H2,5,6)

InChI key

FQPSGWSUVKBHSU-UHFFFAOYSA-N

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This Item
151238M55909276685
Methacrylamide 98%

109606

Methacrylamide

Glycidyl methacrylate 97%, contains 100 ppm monomethyl ether hydroquinone as inhibitor

151238

Glycidyl methacrylate

Methyl methacrylate contains ≤30 ppm MEHQ as inhibitor, 99%

M55909

Methyl methacrylate

Methacrylic anhydride contains 2,000 ppm topanol A as inhibitor, ≥94%

276685

Methacrylic anhydride

form

solid

form

liquid

form

-

form

liquid

mp

106-110 °C (lit.)

mp

-

mp

−48 °C (lit.)

mp

-

General description

Methacrylamide is a functional monomer used inthe preparation of thermo-sensitive hydrogels, polymer latexes, and self-etchingprimers with a longer shelf life. It can also be used to prepare dispersionsuspensions to synthesize biocompatible HA/sol-gel glass mixtures.

pictograms

Exclamation markHealth hazard

signalword

Warning

Hazard Classifications

Acute Tox. 4 Oral - Eye Irrit. 2 - STOT RE 2 - STOT SE 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk_germany

WGK 2

ppe

dust mask type N95 (US), Eyeshields, Faceshields, Gloves


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Asanka Wijekoon et al.
Acta biomaterialia, 9(3), 5653-5664 (2012-11-07)
In this study a series of novel, biocompatible hydrogels able to repeatedly takeup and deliver oxygen at beneficial levels have been developed by conjugating various perfluorocarbon (PFC) chains to methacrylamide chitosan via Schiff base nucleophilic substitution, followed by photopolymerization to
Jian-Lian Chen et al.
Electrophoresis, 32(3-4), 398-407 (2011-02-08)
Nanoparticles exhibiting favorable surface-to-volume ratios create efficient stationary phases for electrochromatography. New nanomaterials derived from chitosan (CS) were immobilized onto modified capillaries for use as the chiral stationary phase (CSP) in open-tubular electrochromatography. This immobilization was achieved through the copolymerization
Elizabeth F Irwin et al.
Biomaterials, 32(29), 6912-6919 (2011-07-22)
We have developed a synthetic polymer interface for the long-term self-renewal of human embryonic stem cells (hESCs) in defined media. We successfully cultured hESCs on hydrogel interfaces of aminopropylmethacrylamide (APMAAm) for over 20 passages in chemically-defined mTeSR™1 media and demonstrated
Ali Ghadban et al.
Biomacromolecules, 13(10), 3108-3119 (2012-08-30)
Ionotropic gelation is particularly appealing for the formation of hydrogels because it takes place under mild conditions, is not thermoreversible, and does not involve toxic chemicals. A well-known example is the gelation of alginate in the presence of calcium ions
Sascha Engelhardt et al.
Biofabrication, 3(2), 025003-025003 (2011-05-13)
Two-photon polymerization (TPP) offers the possibility of creating artificial cell scaffolds composed of micro- and nanostructures with spatial resolutions of less than 1 µm. For use in tissue engineering, the identification of a TPP-processable polymer that provides biocompatibility, biofunctionality and

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