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Sigma-Aldrich

3-(Trimethoxysilyl)propyl acrylate

92%, contains 100 ppm BHT as inhibitor

Synonym(s):

(3-Acryloyloxypropyl)trimethoxysilane

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About This Item

Linear Formula:
H2C=CHCO2(CH2)3Si(OCH3)3
CAS Number:
4369-14-6
Molecular Weight:
234.32
Beilstein:
2046320
MDL number:
MFCD00054803
UNSPSC Code:
12162002
PubChem Substance ID:
24871085
NACRES:
NA.23

Quality Level

100

Assay

92%

contains

100 ppm BHT as inhibitor

refractive index

n20/D 1.429 (lit.)

bp

68 °C/0.4 mmHg (lit.)

density

1.055 g/mL at 25 °C (lit.)

SMILES string

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

InChI

1S/C9H18O5Si/c1-5-9(10)14-7-6-8-15(11-2,12-3)13-4/h5H,1,6-8H2,2-4H3

InChI key

KBQVDAIIQCXKPI-UHFFFAOYSA-N

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General description

3-(Trimethoxysilyl)propyl acrylate is a reactive monomer that is majorly used as a silane coupling agent for the formation of hybrid compounds. It facilitates the formation of a hydrophobic surface by lowering the surface tension and increasing the wettability.

Pictograms

CorrosionExclamation mark
GHS05,GHS07

Signal Word

Danger

Hazard Statements

H314,H317,H332,H412

Hazard Classifications

Acute Tox. 4 Inhalation - Aquatic Chronic 3 - Eye Dam. 1 - Skin Corr. 1B - Skin Sens. 1

Storage Class Code

8A - Combustible corrosive hazardous materials

WGK

WGK 3

Flash Point(F)

253.4 °F - closed cup

Flash Point(C)

123 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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The purpose of this study was to determine whether the brushing durability of a titanium dioxide coating on a polymethyl methacrylate (PMMA) substrate was improved by prior treatment with an acryloxypropyl trimethoxysilane-based agent. Titanium dioxide coatings were obtained by spray-coating
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Additive manufacturing permits innovative soft device architectures with micron resolution. The processing requirements, however, restrict the available materials, and joining chemically dissimilar components remains a challenge. Here we report silicone double networks (SilDNs) that participate in orthogonal crosslinking mechanisms-photocurable thiol-ene
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