175617
(3-Mercaptopropyl)trimethoxysilane
95%
Synonym(s):
3-(Trimethoxysilyl)-1-propanethiol
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About This Item
Linear Formula:
HS(CH2)3Si(OCH3)3
CAS Number:
Molecular Weight:
196.34
UNSPSC Code:
12352103
NACRES:
NA.23
PubChem Substance ID:
EC Number:
224-588-5
Beilstein/REAXYS Number:
2038119
MDL number:
InChI key
UUEWCQRISZBELL-UHFFFAOYSA-N
InChI
1S/C6H16O3SSi/c1-7-11(8-2,9-3)6-4-5-10/h10H,4-6H2,1-3H3
SMILES string
CO[Si](CCCS)(OC)OC
assay
95%
form
liquid
Quality Level
refractive index
n20/D 1.444 (lit.)
bp
213-215 °C (lit.)
density
1.057 g/mL at 25 °C (lit.)
storage temp.
2-8°C
General description
(3-Mercaptopropyl) trimethoxysilane (MPS) is predominantly used as a precursor for silica.
(3-mercaptopropyl)trimethoxysilane (MPTMS) is an organosilane with a thiol group, which can be used as a self-assembled monolayer (SAM). It can be used as a conjunction reagent to immobilize a variety of nanoparticles.
Application
MPTMS can be coated with TiO2, CeO2 and La2O3 for protection against corrosion on quaternary bronze in urban atmosphere. It can also be used as a silica nanofluid (NF) to modify the surface of berea sandstone to improve the enhanced oil recovery (EOR) area in the petroleum industry. MPTMS forms composites with kaolin, that can be used as an absorbent for the removal of heavy metals from wastewater. MPTMS can form a bilayer with multiwalled carbon nanotubes (MWNTs) on gold electrodes which can be used to study the electrochemical properties of fluphenazine.
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Aquatic Chronic 2 - Skin Sens. 1
Storage Class
10 - Combustible liquids
wgk
WGK 2
flash_point_f
204.8 °F - closed cup
flash_point_c
96 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
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Eduardo Reátegui et al.
Nature communications, 9(1), 175-175 (2018-01-14)
Extracellular vesicles (EVs) carry RNA, DNA, proteins, and lipids. Specifically, tumor-derived EVs have the potential to be utilized as disease-specific biomarkers. However, a lack of methods to isolate tumor-specific EVs has limited their use in clinical settings. Here we report
XPS and electrochemical evaluation of two-dimensional organic films obtained by chemical modification of self-assembled monolayers of (3-mercaptopropyl) trimethoxysilane on copper surfaces.
Sinapi F, et al.
Materials Science & Engineering. C, Materials For Biological Applications, 22(2), 345-353 (2002)
Lining Ju et al.
Scientific reports, 7(1), 14185-14185 (2017-10-29)
Conventional approaches for studying receptor-mediated cell signaling, such as the western blot and flow cytometry, are limited in three aspects: 1) The perturbing preparation procedures often alter the molecules from their native state on the cell; 2) Long processing time
Hydrolysis and condensation of self-assembled monolayers of (3-mercaptopropyl) trimethoxysilane on Ag and Au surfaces."
Thompson WR, et al.
Langmuir, 13(8), 2291-2302 (1997)
Synthesis and luminescence of (3-mercaptopropyl)-trimethoxysilane capped CdS quantum dots
Wuister SF, et al.
Journal of Luminescence, 102, 338-343 (2003)
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