3179-76-8 Usage
Description
3-Aminopropyl-methyl-diethoxysilane, also known as (3-aminopropyl)diethoxymethylsilane, is a colorless transparent liquid that serves as a silane coupling agent. It is a versatile chemical compound with a unique structure that includes an aminopropyl group, a methyl group, and two diethoxysilane groups. This combination of functional groups allows it to form strong covalent bonds with various materials, making it a valuable component in a wide range of applications.
Uses
Used in Chemical Industry:
3-Aminopropyl-methyl-diethoxysilane is used as a silane coupling agent for enhancing the adhesion and compatibility between different materials. Its ability to form strong covalent bonds with a variety of substrates, such as glass, metal, and polymers, makes it an essential component in the production of coatings, adhesives, and sealants.
Used in Nanotechnology:
3-Aminopropyl-methyl-diethoxysilane is used as a precursor in the synthesis of nanoparticles and nanocomposites. Its functional groups enable the formation of stable colloidal suspensions and the development of novel materials with improved properties, such as enhanced mechanical strength, thermal stability, and electrical conductivity.
Used in Surface Modification:
3-Aminopropyl-methyl-diethoxysilane is used for modifying the surface properties of materials, such as improving their hydrophilicity, wettability, or biocompatibility. This surface modification can be applied to various materials, including plastics, ceramics, and metals, to tailor their properties for specific applications, such as biomedical devices, sensors, or environmental remediation technologies.
Used in Aromatics Industry:
3-Aminopropyl-methyl-diethoxysilane is used in the preparation of aromatic imine monolayers. The reaction of this silane coupling agent with aromatic imines results in the formation of well-ordered monolayers with potential applications in sensors, catalysis, and molecular electronics.
Flammability and Explosibility
Nonflammable
Safety Profile
Poison by intraperitoneal route.Moderately toxic by ingestion and skin contact. A skinirritant. When heated to decomposition it emits toxicfumes of NOx.
Check Digit Verification of cas no
The CAS Registry Mumber 3179-76-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,1,7 and 9 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 3179-76:
(6*3)+(5*1)+(4*7)+(3*9)+(2*7)+(1*6)=98
98 % 10 = 8
So 3179-76-8 is a valid CAS Registry Number.
InChI:InChI=1/C8H21NO2Si/c1-4-10-12(3,11-5-2)8-6-7-9/h4-9H2,1-3H3
3179-76-8Relevant articles and documents
ORGANOSILICON COMPOUND AND ITS PRODUCTION METHOD, COMPOUNDING AGENT FOR RUBBER, RUBBER COMPOSITION, AND TIRE
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, (2012/12/13)
A method for producing a sulfur-containing organosilicon compound capable of dramatically reducing hysteresis loss of the cured rubber composition and improving abrasion resistance and its production method are provided. A compounding agent for rubber containing the sulfur-containing organosilicon compound, a rubber composition prepared by blending such compounding agent for rubber, and a tire produced by using the cured rubber composition are also provided. The sulfur-containing organosilicon compound has a hydrolyzable silyl group, amino group, and mercapto group.
Platinum oxide (PtO2): A potent hydrosilylation catalyst
Sabourault, Nicolas,Mignani, Gerard,Wagner, Alain,Mioskowski, Charles
, p. 2117 - 2119 (2007/10/03)
(matrix presented) Platinum oxide was found to be a versatile and powerful hydrosilylation catalyst upon a wide variety of functionalized alkenes and especially aminated alkenes. Moreover, highly reproducible results and easy removal make this new catalys
Process for making a silylisocyanurate
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, (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.