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Sigma-Aldrich

Trimethoxy(2-phenylethyl)silane

98%

Synonym(s):

(2-Phenylethyl)trimethoxysilane

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About This Item

Linear Formula:
C6H5CH2CH2Si(OCH3)3
CAS Number:
49539-88-0
Molecular Weight:
226.34
Beilstein/REAXYS Number:
3031224
EC Number:
256-363-2
MDL number:
MFCD00053852
UNSPSC Code:
12352103
PubChem Substance ID:
24867446
NACRES:
NA.23

assay

98%

form

liquid

refractive index

n20/D 1.475 (lit.)

bp

95-96 °C/2 mmHg (lit.)

density

1.033 g/mL at 25 °C (lit.)

SMILES string

CO[Si](CCc1ccccc1)(OC)OC

InChI

1S/C11H18O3Si/c1-12-15(13-2,14-3)10-9-11-7-5-4-6-8-11/h4-8H,9-10H2,1-3H3

InChI key

UBMUZYGBAGFCDF-UHFFFAOYSA-N

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General description

Trimethoxy(2-phenylethyl)silane (TMPES) is a phenyl functionalized trialkoxy silane that can be used as a siloxane based precursor.

Application

TMPES can be used as a silane-based coating on quantum dot (QD) light emitting diodes to improve the adhesion of QDs and improve the thermal stability of the device. It may be used in the synthesis of pure silica zeolite molecular sieves.

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

10 - Combustible liquids

wgk_germany

WGK 3

flash_point_f

222.8 °F - closed cup

flash_point_c

106 °C - closed cup

ppe

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

Certificates of Analysis (COA)

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Organic-functionalized molecular sieves as shape-selective catalysts
Jones CW, et al.
Nature, 393(6680), 52-52 (1998)
Hydrolysis-condensation kinetics of different silane coupling agents
Brochier S, et al.
Phosphorus, Sulfur, and Silicon and the Related Elements, 186(2), 240-254 (2011)
Quantum dot-layer-encapsulated and phenyl-functionalized silica spheres for highly luminous, colour rendering, and stable white light-emitting diodes
Yoo H, et al.
Nanoscale, 7(30), 12860-12867 (2015)
Louise Stjern et al.
International journal of pharmaceutics, 531(2), 595-605 (2017-05-31)
Cyclodextrins (CDs) and mesoporous silica particles (MSPs) have been combined as composite carriers for controlled antibiotic release. CDs were employed as "gatekeeper" agents and grafted onto MSPs to retain drug molecules inside the MSP carrier. A variety of CDs (unfunctionalized
Emre Seyyal et al.
Analytica chimica acta, 964, 96-111 (2017-03-30)
Principles of sol-gel chemistry were utilized to create silica- and germania-based dual-ligand surface-bonded sol-gel coatings providing enhanced performance in capillary microextraction (CME) through a combination of ligand superhydrophobicity and π-π interaction. These organic-inorganic hybrid coatings were prepared using sol-gel precursors
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