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M6514

Sigma-Aldrich

3-(Trimethoxysilyl)propyl methacrylate

≥97%

Synonym(s):

Silane A174, [3-(Methacryloyloxy)propyl]trimethoxysilane

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25 ML
CN¥643.66
50 ML
CN¥852.80

CN¥643.66

Estimated to ship onApril 07, 2025Details

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25 ML
CN¥643.66
50 ML
CN¥852.80

About This Item

Linear Formula:
H2C=C(CH3)CO2(CH2)3Si(OCH3)3
CAS Number:
2530-85-0
Molecular Weight:
248.35
Beilstein:
1952435
EC Number:
219-785-8
MDL number:
MFCD00008593
UNSPSC Code:
47101511
PubChem Substance ID:
24897091
NACRES:
NA.56

CN¥643.66

Estimated to ship onApril 07, 2025Details

Request a Bulk Order

Assay

≥97%

form

liquid

refractive index

n20/D 1.431 (lit.)

bp

190 °C (lit.)

density

1.045 g/mL at 25 °C (lit.)

storage temp.

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

InChI key

XDLMVUHYZWKMMD-UHFFFAOYSA-N

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1 of 4

This Item
440159551635234893
3-(Trimethoxysilyl)propyl methacrylate ≥97%

M6514

3-(Trimethoxysilyl)propyl methacrylate

3-(Trimethoxysilyl)propyl methacrylate 98%

440159

3-(Trimethoxysilyl)propyl methacrylate

Trimethoxy[3-(methylamino)propyl]silane 95%

551635

Trimethoxy[3-(methylamino)propyl]silane

Ethyl methacrylate contains 15-20 ppm monomethyl ether hydroquinone as inhibitor, 99%

234893

Ethyl methacrylate

density

1.045 g/mL at 25 °C (lit.)

density

1.045 g/mL at 25 °C (lit.)

density

0.975 g/mL at 25 °C (lit.)

density

0.917 g/mL at 25 °C (lit.)

Quality Level

100

Quality Level

200

Quality Level

200

Quality Level

200

bp

190 °C (lit.)

bp

190 °C (lit.)

bp

106 °C (lit.)

bp

118-119 °C (lit.)

refractive index

n20/D 1.431 (lit.)

refractive index

n20/D 1.431 (lit.)

refractive index

-

refractive index

n20/D 1.413 (lit.)

storage temp.

2-8°C

storage temp.

-

storage temp.

-

storage temp.

2-8°C

General description

3-(Trimethoxysilyl)propyl methacrylate (TMSPMA) is a hydrophobic monomer.[1] The presence of an additional functional group of acrylate facilitates TMSPMA for grafting polymerization on plastic surfaces.[2] 3-(Trimethoxysilyl)propyl methacrylate undergoes first-order kinetic polymerization to form polyTMSPMA, which is a moisture stable polymer.[3]

Application

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.[4]
  • 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.[5]
  • 3-(Trimethoxysilyl)propyl methacrylate is also used in the preparation of organic/inorganic hybrid nanomaterials.[6]

Packaging

A product Information sheet is supplied which describes procedures for using this product.

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Product No.
Description
Pricing

Storage Class Code

10 - Combustible liquids

WGK

WGK 1

Flash Point(F)

197.6 °F - closed cup

Flash Point(C)

92 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves
  • Specification Sheet

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    Certificates of Analysis (COA)

    Lot/Batch Number
    MKCT4433
    MKCR5502
    MKCK3155
    MKCG8995
    MKBX0874V

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    ATRP of 3-(triethoxysilyl)propyl methacrylate and preparation of ?stable? gelable block copolymers
    Ming Xiong
    European Polymer Journal, 44, 3835-3841 (2008)
    Method for attachment of microscopic preparations on glass for in situ hybridization, PRINS and in situ PCR studies.
    H M Dyanov et al.
    BioTechniques, 18(5), 822-824 (1995-05-01)
    Bozhen Zhang et al.
    Journal of materials chemistry. B, 9(35), 7196-7204 (2021-07-23)
    Label-free cell sorting devices are of great significance for biomedical research and clinical therapeutics. However, current platforms for label-free cell sorting cannot achieve continuity and selectivity simultaneously, resulting in complex steps and limited reliability. Here, an immunoaffinity-based cell catch-transport-release thermo-chemo-mechanical
    Sean Brahim et al.
    Biomacromolecules, 4(5), 1224-1231 (2003-09-10)
    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
    M Aguadé et al.
    Proceedings of the National Academy of Sciences of the United States of America, 91(11), 4658-4662 (1994-05-24)
    Single-strand conformation polymorphism (SSCP) analysis followed by DNA sequencing of stratified sub-samples was used to survey DNA polymorphism in the su(s) and su(wa) regions in a natural population of Drosophila melanogaster. su(s) and su(wa) are located near the telomere of
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