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重要文件

551635

Sigma-Aldrich

三甲氧基[3-(甲氨基)丙基]硅烷

95%

同義詞:

N-甲基-3-(三甲氧基甲硅基)丙胺, [3-(甲氨基)丙基]三甲氧基硅烷

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About This Item

線性公式:
(CH3O)3Si(CH2)3NHCH3
CAS號碼:
分子量::
193.32
Beilstein:
2072720
EC號碼:
MDL號碼:
分類程式碼代碼:
12352103
PubChem物質ID:
NACRES:
NA.23
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化驗

95%

形狀

liquid

bp

106 °C (lit.)

密度

0.975 g/mL at 25 °C (lit.)

SMILES 字串

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 密鑰

DVYVMJLSUSGYMH-UHFFFAOYSA-N

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一般說明

三甲氧基[3-(甲基氨基)丙基]硅烷(MAPTMS)是一种可用于硅烷化表面固定的氨基烷基三甲氧基硅烷。[1][2]

應用

MAPTMS可以对SBA-15进行功能化修饰,后者有望用于吸收二氧化碳(CO2)以及用于新型传感器。[3][4]它也可以用于制备质子传导膜。[5]
将三甲氧基 [3-(甲氨基)丙基] 硅烷涂覆到基底上,通过聚合金纳米球制备金二聚体。[6] 硅烷可作为硅烷偶联剂制备二氧化硅纳米颗粒。2 可用于改性石英基片。[7]

特點和優勢

  • 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.

象形圖

Corrosion

訊號詞

Danger

危險聲明

危險分類

Eye Dam. 1

儲存類別代碼

10 - Combustible liquids

水污染物質分類(WGK)

WGK 3

閃點(°F)

179.6 °F - closed cup

閃點(°C)

82 °C - closed cup

個人防護裝備

Eyeshields, Gloves, type ABEK (EN14387) respirator filter


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存取文件庫

Functionalization of delaminated zeolite ITQ-6 for the adsorption of carbon dioxide.
Zukal A, et al.
Langmuir, 25(17), 10314-10321 (2009)
Amine-modified titania-silica hybrid gels as epoxidation catalysts.
Muller, CA, et al.
Applied Catalysis A: General, 201(2), 253-261 (2000)
Near-field imaging of surface-enhanced Raman active sites in aggregated gold nanoparticles.
Chemistry Letters (Jpn), 35(1), 78-79 (2006)
Vinyl sulfone: a versatile function for simple bioconjugation and immobilization.
Morales-Sanfrutos J, et al.
Organic & Biomolecular Chemistry, 8(3), 667-675 (2010)
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

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