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Merck
CN

408123

[2-(Methacryloyloxy)ethyl]trimethylammonium methyl sulfate solution

80 wt. % in H2O

Synonym(s):

β-Methacryloyloxyethyltrimethylammonium methosulfate, (Methacryloyloxy)ethyltrimethylammonium methosulfate, (Trimethylammonio)ethyl methacrylate methyl sulfate, Ethanaminium, N ,N ,N -trimethyl-2-[(2-methyl-1-oxo-2-propenyl)oxy]-methyl sulfate

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About This Item

Linear Formula:
H2C=C(CH3)CO2CH2CH2N(CH3)3(OSO3CH3)
CAS Number:
6891-44-7
Molecular Weight:
283.34
UNSPSC Code:
12162002
PubChem Substance ID:
24865506
MDL number:
MFCD00078263

Key Documents

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InChI

1S/C9H18NO2.CH4O4S/c1-8(2)9(11)12-7-6-10(3,4)5;1-5-6(2,3)4/h1,6-7H2,2-5H3;1H3,(H,2,3,4)/q+1;/p-1

SMILES string

COS([O-])(=O)=O.CC(=C)C(=O)OCC[N+](C)(C)C

InChI key

IHBKAGRPNRKYAO-UHFFFAOYSA-M

contains

900 ppm monomethyl ether hydroquinone as inhibitor

concentration

80 wt. % in H2O

refractive index

n20/D 1.443

density

1.183 g/mL at 25 °C

pictograms

Exclamation mark
GHS07

signalword

Warning

hcodes

H315

Hazard Classifications

Skin Irrit. 2

Storage Class

10 - Combustible liquids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

Regulatory Information

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Certificates of Analysis (COA)

Lot/Batch Number
08718AD
08409DF

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Alicia K Friedman et al.
Soft matter, 12(47), 9477-9484 (2016-11-17)
Synthetic hydrogels were utilized to explore influence of both charge and phenylalanine-glycine (FG) repeat concentration on translocation of select proteins. Hydrogels studied represent a biomimetic platform of the nuclear pore complex (NPC) found in eukaryotic cells. Polyacrylamide/phenylalanine-serine-phenylalanine-glycine (FSFG) peptide copolymers
A Tezvergil-Mutluay et al.
Journal of dental research, 90(4), 535-540 (2011-01-08)
Matrix metalloproteinases (MMPs) bound to dentin contribute to the progressive degradation of collagen fibrils in hybrid layers created by dentin adhesives. This study evaluated the MMP-inhibiting potential of quaternary ammonium methacrylates (QAMs), with soluble rhMMP-9 and a matrix-bound endogenous MMP
C W Fuller et al.
European journal of biochemistry, 103(2), 421-430 (1980-01-01)
Using a new and simplified technique for covalent immobilization of adenine nucleotides [Fuller, C. W. and Bright, H. J., J. Biol. Chem. 252, 6631 (1977)], we have prepared immobilized NADH using two water-soluble polymers and tested these preparations for activity

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