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175617

Sigma-Aldrich

(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:
4420-74-0
Molecular Weight:
196.34
Beilstein:
2038119
EC Number:
224-588-5
MDL number:
MFCD00004901
UNSPSC Code:
12352103
PubChem Substance ID:
24850516
NACRES:
NA.23

Assay

95%

form

liquid

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

SMILES string

CO[Si](CCCS)(OC)OC

InChI

1S/C6H16O3SSi/c1-7-11(8-2,9-3)6-4-5-10/h10H,4-6H2,1-3H3

InChI key

UUEWCQRISZBELL-UHFFFAOYSA-N

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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.

Pictograms

Exclamation markEnvironment
GHS07,GHS09

Signal Word

Warning

Hazard Statements

H302,H317,H411

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Chronic 2 - Skin Sens. 1

Storage Class Code

10 - Combustible liquids

WGK

WGK 2

Flash Point(F)

204.8 °F - closed cup

Flash Point(C)

96 °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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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)
Response surface approach for optimization of Hg (II) adsorption by 3-mercaptopropyl trimethoxysilane-modified kaolin minerals from aqueous solution.
Yilmaz S et al.
Korean Journal of Chemical Engineering, 34(8), 2225-2235 (2017)
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)
Baizhao Zeng et al.
Talanta, 64(2), 380-386 (2008-10-31)
A novel multi-walled carbon nanotubes/(3-mercaptopropyl)trimethoxysilane (MPS) bilayer modified gold electrode was prepared and used to study the electrochemcial behavior of fluphenazine and determine it. Fluphenazine could effectively accumulate at this electrode and produce two anodic peaks at about 0.78V and
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