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Merck
모든 사진(1)

주요 문서

551635

Sigma-Aldrich

Trimethoxy[3-(methylamino)propyl]silane

95%

동의어(들):

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

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크기 선택

25 ML
₩136,112
100 ML
₩401,636

₩136,112


예상 입고일2025년 4월 21일세부사항


벌크 견적 요청

크기 선택

보기 변경
25 ML
₩136,112
100 ML
₩401,636

About This Item

Linear Formula:
(CH3O)3Si(CH2)3NHCH3
CAS Number:
Molecular Weight:
193.32
Beilstein:
2072720
EC Number:
MDL number:
UNSPSC 코드:
12352103
PubChem Substance ID:
NACRES:
NA.23

₩136,112


예상 입고일2025년 4월 21일세부사항


벌크 견적 요청

Quality Level

분석

95%

양식

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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일반 설명

Trimethoxy[3-(methylamino)propyl] silane, also known as N-Methyl-3-(trimethoxysilyl)propylamine, is an aminoalkyl silane compound widely utilized in surface modification and as a precursor in the synthesis of functionalized materials. It is primarily employed for its ability to modify surfaces through silanization. This process enhances the adhesion properties of substrates, making it valuable in coatings, adhesives, and composites.

애플리케이션

  • Trimethoxy[3-(methylamino)propyl] silane is used ; As an amino precursor to synthesize nickel modified amino silica sols via hydrolysis method. which induces the formation of microporous membranes for methanol-selective, high-flux pervaporation. [1]
  • As a silane coupling agent in the synthesis of RuCl3/ZrSBA-15-AP catalysts, which facilitate the hydrogenation of CO2 to produce formic acid. [2]
  • As an amino polymer used in the modification of black phosphorus nanosheets, which are employed in sensors to detect trace amounts of CO2 at room temperature. [3]
  • in the surface modification of Au@SiO2 nanoparticles to create positively or negatively charged surfaces. This modification is utilized in Cu-doped TiO2 electrodes for electrochemiluminescence sensing applications. [4]
Trimethoxy[3-(methylamino)propyl]silane was coated onto a substrate for the preparation of gold dimers by aggregating gold nanospheres. [5] The silane may be used as a silane coupling agent to prepare silica nanoparticles. 2 It may be used to modify quartz substrates.[6]

특징 및 장점

  • Silanecoupling agents enhance adhesion between organic and inorganic materials,improving the strength and performance of glass-fiber reinforced plastics.
  • With two functionalgroups—one for organic and one for inorganic materials—this enables versatilebonding and enhanced performance across various materials.

픽토그램

Corrosion

신호어

Danger

유해 및 위험 성명서

예방조치 성명서

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

개인 보호 장비

Eyeshields, Gloves, type ABEK (EN14387) respirator filter


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문서 라이브러리 방문

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
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)
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)
Vinyl sulfone: a versatile function for simple bioconjugation and immobilization.
Morales-Sanfrutos J, et al.
Organic & Biomolecular Chemistry, 8(3), 667-675 (2010)
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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