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About This Item
Linear Formula:
H2C=C(CH3)CO2(CH2)3Si(OCH3)3
CAS Number:
Molecular Weight:
248.35
UNSPSC Code:
47101511
NACRES:
NA.56
PubChem Substance ID:
EC Number:
219-785-8
Beilstein/REAXYS Number:
1952435
MDL number:
Product Name
3-(Trimethoxysilyl)propyl methacrylate, ≥97%
InChI key
XDLMVUHYZWKMMD-UHFFFAOYSA-N
InChI
1S/C10H20O5Si/c1-9(2)10(11)15-7-6-8-16(12-3,13-4)14-5/h1,6-8H2,2-5H3
SMILES string
CO[Si](CCCOC(=O)C(C)=C)(OC)OC
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
Quality Level
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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.
- 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.
General description
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.
Packaging
A product Information sheet is supplied which describes procedures for using this product.
Storage Class
10 - Combustible liquids
wgk
WGK 1
flash_point_f
197.6 °F - closed cup
flash_point_c
92 °C - closed cup
ppe
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
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Preparation of organic/inorganic hybrid nanomaterials using aggregates of poly (stearyl methacrylate)-b-poly (3-(trimethoxysilyl) propyl methacrylate) as precursor.
Junfeng Zhou.
Eur. Polymer J., 5, 1736-1743 (2007)
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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
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)
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