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CAS:60111-47-9 | 3-[(dimethylvinylsilyl)oxy]-1,1,5,5-tetramethyl-3-phenyl-1,5-divinyltrisiloxane

CAS:60111-47-9 | 3-[(dimethylvinylsilyl)oxy]-1,1,5,5-tetramethyl-3-phenyl-1,5-divinyltrisiloxane

Molecular Formula:C18H32O3Si4
Molecular Weight:408.79
EINECS:262-056-4
Package:5g 25g 100g
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Product Introduction

Introduction of CAS:60111-47-9 | 3-[(dimethylvinylsilyl)oxy]-1,1,5,5-tetramethyl-3-phenyl-1,5-divinyltrisiloxane

 

Tris(vinyldimethylsiloxy)phenylsilane, also known as TDMPS, is a silane compound with a vinyl group on the siloxy bridge and a phenyl group attached to the silicon atom. It is an important chemical in the field of organic synthesis, as it is a versatile reagent used in many different types of reactions. TDMPS has been studied extensively for its unique properties, which make it useful in a variety of applications.

 

Specification of CAS:60111-47-9 | 3-[(dimethylvinylsilyl)oxy]-1,1,5,5-tetramethyl-3-phenyl-1,5-divinyltrisiloxane

 

ITEMS

SPECIFICATION

Boiling point

112~115℃/2mm

Purity

98%

Refractive index

1.4580 to 1.4620

Density

0.950 g/cm3

Color

Colorless to almost colorless

Form

transparency liquid

 

Research Application of CAS:60111-47-9 | 3-[(dimethylvinylsilyl)oxy]-1,1,5,5-tetramethyl-3-phenyl-1,5-divinyltrisiloxane

 

Surfactant Behavior and Micellization

Tris(vinyldimethylsiloxy)phenylsilane has been studied for its surfactant behavior. Chen and Tan (2020) synthesized and confirmed various trisiloxane surfactants, including bis(vinyldimethylsiloxy)methylsilylpropyl-imidazolium chloride, through techniques like NMR and mass spectrometry. They explored the micellization behavior of these compounds, finding that the critical micelle concentration values varied with the hydrophobicity of the siloxane groups and the cationic head groups. This research highlights the potential of tris(vinyldimethylsiloxy)phenylsilane derivatives in surfactant applications (Chen & Tan, 2020).

 

Polymer Synthesis and Study

Shapkin et al. (1989) researched the synthesis of three-dimensional polymers using tris-(3-chlorosulphenyl-2,4-pentadionates) of various metals with vinylsiloxane, a compound related to tris(vinyldimethylsiloxy)phenylsilane. They succeeded in obtaining crosslinked polyorganosiloxanes, providing insights into creating polymers with metal-tris-(3-chlorethylthio-2,4-pentanodionate) fragments in their backbone. This study opens up possibilities for the use of tris(vinyldimethylsiloxy)phenylsilane derivatives in innovative polymer synthesis (Shapkin, Svistunov & Shapkina, 1989).

 

Photoinitiation in Polymerization

Semenov et al. (1990) found that organopolysilanes, including trisilanes with structures similar to tris(vinyldimethylsiloxy)phenylsilane, are effective photoinitiators for the polymerization of vinyl-containing siloxane rubbers. Their research demonstrates the utility of such compounds in the photocuring process of polymers, suggesting potential applications in materials science and engineering (Semenov, Cherepennikova, Artemicheva & Razuvaev, 1990).

 

Organic Electroluminescence Devices

Research by Shu and Jing-Cu (2008) on conducting polymer polydimethylsiloxane (PDMS) for organic electroluminescence devices indirectly highlights the potential of tris(vinyldimethylsiloxy)phenylsilane-related compounds in the field of organic electronics. They investigated the preparation of an electrode consisting of a SiC thin film and PDMS, leading to insights into the conductivity and device properties in organic semiconductors. This research suggests the relevance of tris(vinyldimethylsiloxy)phenylsilane derivatives in the development of high-performance electrodes for organic electronic applications (Shu & Jing-Cu, 2008).

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