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M6514

Sigma-Aldrich

3-(Trimethoxysilyl)propylmethacrylat

≥97%

Synonym(e):

Silan A174, [3-(Methacryloyloxy)propyl]trimethoxysilan

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About This Item

Lineare Formel:
H2C=C(CH3)CO2(CH2)3Si(OCH3)3
CAS-Nummer:
2530-85-0
Molekulargewicht:
248.35
Beilstein:
1952435
EG-Nummer:
219-785-8
MDL-Nummer:
MFCD00008593
UNSPSC-Code:
47101511
PubChem Substanz-ID:
24897091
NACRES:
NA.56

Qualitätsniveau

100

Assay

≥97%

Form

liquid

Brechungsindex

n20/D 1.431 (lit.)

bp

190 °C (lit.)

Dichte

1.045 g/mL at 25 °C (lit.)

Lagertemp.

2-8°C

SMILES String

CO[Si](CCCOC(=O)C(C)=C)(OC)OC

InChI

1S/C10H20O5Si/c1-9(2)10(11)15-7-6-8-16(12-3,13-4)14-5/h1,6-8H2,2-5H3

InChIKey

XDLMVUHYZWKMMD-UHFFFAOYSA-N

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Allgemeine Beschreibung

3-(Trimethoxysilyl)propyl methacrylate (TMSPMA) is a hydrophobic monomer. The presence of an additional functional group of acrylate facilitates TMSPMA for grafting polymerization on plastic surfaces. 3-(Trimethoxysilyl)propyl methacrylate undergoes first-order kinetic polymerization to form polyTMSPMA, which is a moisture stable polymer.

Anwendung

3-(Trimethoxysilyl)propyl methacrylate has been used in the following applications:
  • Isoelectric focusing can lead to pH gradient formation resulting in the swelling or shrinking of gel casts. This can be prevented by using 3-(Trimethoxysilyl)propyl methacrylate to link polyacrylamide gels to glass plates covalently.
  • In situ hybridization using 3-(Trimethoxysilyl)propyl methacrylate along with poly-L-lysine is a faster and durable method to attach cells, microscopic sections, and total organs to slides/other glass surfaces.
  • 3-(Trimethoxysilyl)propyl methacrylate is also used in the preparation of organic/inorganic hybrid nanomaterials.

Verpackung

Ein Produktdatenblatt mit der Beschreibung der Anwendung dieses Produktes wird mitgeliefert.

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Lagerklassenschlüssel

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WGK

WGK 1

Flammpunkt (°F)

197.6 °F - closed cup

Flammpunkt (°C)

92 °C - closed cup

Persönliche Schutzausrüstung

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

Analysenzertifikate (COA)

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Sigma-Aldrich

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An amphiphilic hydrogel of poly(2-hydroxyethyl methacrylate) cross-linked with tetraethyleneglycol diacrylate (TEGDA) was synthesized to contain the hydrophobic monomer 3-(trimethoxy-silyl) propyl methacrylate (PMA) and the pH-responsive, hydrophilic monomer N',N'-dimethylaminoethyl methacrylate (DMAEMA). The gels were separately loaded with two biomolecular probes, insulin
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