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4-Aminobutyltriethoxysilane, an organosilicon chemical compound, is widely utilized in material science and surface chemistry. It is recognized for its ability to create a robust bond between organic and inorganic materials, serving as an adhesion promoter, coupling agent, or crosslinker. This versatile compound is a crucial element in sol-gel technology and is particularly known for enhancing the adhesion of polymers, thereby improving the performance of composite materials. However, due to its potentially harmful nature, it is essential to exercise proper safety measures during its handling.

3069-30-5

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3069-30-5 Usage

Uses

Used in Material Science:
4-Aminobutyltriethoxysilane is used as an adhesion promoter for improving the bond strength between organic and inorganic materials, which is crucial for the development of high-performance composite materials.
Used in Surface Chemistry:
In surface chemistry, 4-Aminobutyltriethoxysilane functions as a coupling agent, facilitating the interaction between different materials and enhancing their compatibility.
Used in Sol-Gel Technology:
4-Aminobutyltriethoxysilane is employed as a crosslinker in sol-gel technology, contributing to the formation of stable and durable materials with unique properties.
Used in Composite Material Production:
4-Aminobutyltriethoxysilane is used as a key component in the production of composite materials, where it enhances the adhesion of polymers, leading to improved overall performance.

Check Digit Verification of cas no

The CAS Registry Mumber 3069-30-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,0,6 and 9 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 3069-30:
(6*3)+(5*0)+(4*6)+(3*9)+(2*3)+(1*0)=75
75 % 10 = 5
So 3069-30-5 is a valid CAS Registry Number.
InChI:InChI=1/C10H25NO3Si/c1-4-12-15(13-5-2,14-6-3)10-8-7-9-11/h4-11H2,1-3H3

3069-30-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-triethoxysilylbutan-1-amine

1.2 Other means of identification

Product number -
Other names Silane,(4-aminobutyl)triethoxy

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:3069-30-5 SDS

3069-30-5Downstream Products

3069-30-5Relevant academic research and scientific papers

Discovering Partially Charged Single-Atom Pt for Enhanced Anti-Markovnikov Alkene Hydrosilylation

Chen, Yuanjun,Ji, Shufang,Sun, Wenming,Chen, Wenxing,Dong, Juncai,Wen, Junfeng,Zhang, Jian,Li, Zhi,Zheng, Lirong,Chen, Chen,Peng, Qing,Wang, Dingsheng,Li, Yadong

supporting information, p. 7407 - 7410 (2018/06/11)

The hydrosilylation reaction is one of the largest-scale application of homogeneous catalysis and is widely used to enable the commercial manufacture of silicon products. However, considerable issues including disposable platinum consumption, undesired side reactions and unacceptable catalyst residues still remain. Here, we synthesize a heterogeneous partially charged single-atom platinum supported on anatase TiO2 (Pt1δ+/TiO2) catalyst via an electrostatic-induction ion exchange and two-dimensional confinement strategy, which can catalyze hydrosilylation reaction with almost complete conversion and produce exclusive adduct. Density functional theory calculations reveal that unexpected property of Pt1δ+/TiO2 originates from atomic dispersion of active species and unique partially positive charge Ptδ+ electronic structure that conventional nanocatalysts do not possess. The fabrication of single-atom Pt1δ+/TiO2 catalyst accomplishes a reasonable use of Pt through recycling and maximum atom-utilized efficiency, indicating the potential to achieve a green hydrosilylation industry.

Process for making a silylisocyanurate

-

, (2008/06/13)

This invention provides a process for making a silylorganocarbamate or a silylisocyanurate which process comprises reacting an aminosilane with a dialkyl carbonate, diaryl carbonate or a mixture thereof in the presence of a basic catalyst to obtain the silylorganocarbamate; optionally, neutralizing the basic catalyst and residual aminosilane with a neutralizing agent; and adding a cracking catalyst and heating at subatmospheric pressure to obtain the silylisocyanurate; or heating a silylorganocarbamate at a temperature sufficient for dissociation of the carbamate at subatmospheric pressure in the presence of a cracking catalyst and a timerization catalyst to obtain a silylisocyanurate.

Azido-silane compositions

-

, (2008/06/13)

Azido-containing silane compositions of matter useful as coupling agents in the production of polymer composite articles.

Azido-silane compositions

-

, (2008/06/13)

Azido-containing silane compositions of matter useful as coupling agents in the production of polymer composite articles.

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