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Sigma-Aldrich

Trimethoxy[3-(methylamino)propyl]silane

95%

Synonym(s):

N-Methyl-3-(trimethoxysilyl)propylamine, [3-(Methylamino)propyl]trimethoxysilane

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About This Item

Linear Formula:
(CH3O)3Si(CH2)3NHCH3
CAS Number:
3069-25-8
Molecular Weight:
193.32
Beilstein:
2072720
EC Number:
221-334-5
MDL number:
MFCD00048021
UNSPSC Code:
12352103
PubChem Substance ID:
24879231
NACRES:
NA.23

Quality Level

200

Assay

95%

form

liquid

bp

106 °C (lit.)

density

0.975 g/mL at 25 °C (lit.)

SMILES string

CNCCC[Si](OC)(OC)OC

InChI

1S/C7H19NO3Si/c1-8-6-5-7-12(9-2,10-3)11-4/h8H,5-7H2,1-4H3

InChI key

DVYVMJLSUSGYMH-UHFFFAOYSA-N

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General description

Trimethoxy[3-(methylamino)propyl]silane (MAPTMS) is an aminoalkyltrimethoxysilane that can be used for silanization surface immobilization.

Application

MAPTMS can functionalize SBA-15 which can potentially be used for the absorption of carbon dioxide(CO2) and also in novel sensors. It can also be used in the preparation of proton conductive membranes.
Trimethoxy[3-(methylamino)propyl]silane was coated onto a substrate for the preparation of gold dimers by aggregating gold nanospheres. The silane may be used as a silane coupling agent to prepare silica nanoparticles. 2 It may be used to modify quartz substrates.

Pictograms

Corrosion
GHS05

Signal Word

Danger

Hazard Statements

H318

Precautionary Statements

P280 - P305 + P351 + P338

Hazard Classifications

Eye Dam. 1

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point(F)

179.6 °F - closed cup

Flash Point(C)

82 °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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Water-soluble conjugated polymer-induced self-assembly of gold nanoparticles and its application to SERS
Langmuir, 24(19), 10608-10611 (2008)
Yujie Zhang et al.
Journal of chromatography. A, 1626, 461366-461366 (2020-08-17)
An alternative method for efficient synthesis of urea-functionalized silanes was proposed on the basis of an N, N'-carbonyldiimidazole-mediated acyl-transfer reaction between various amino-containing building blocks. The employment of different parent aminosilanes and alkylamines afforded an array of urea-containing silanes, which
Covalent organic/inorganic hybrid proton-conductive membrane with semi-interpenetrating polymer network: preparation and characterizations.
Fu R, et al.
Journal of Power Sources, 179(2), 458-466 (2008)
Direct synthesis of highly ordered large-pore functionalized mesoporous SBA-15 silica with methylaminopropyl groups and its catalytic reactivity in flavanone synthesis.
Wang X, et al.
Microporous and Mesoporous Materials : The Official Journal of the International Zeolite Association, 85(3), 241-251 (2005)
Functionalization of delaminated zeolite ITQ-6 for the adsorption of carbon dioxide.
Zukal A, et al.
Langmuir, 25(17), 10314-10321 (2009)
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