7646-75-5

Usage

Uses

Used in Polymer and Composite Production:
Dimethylphenylsilanol sodium salt, 97% is used as a coupling agent or adhesion promoter in the production of polymers and composites. It enhances the compatibility and adhesion between different materials, improving the overall performance and durability of the final product.
Used in Surface Treatment for Various Materials:
In the Surface Treatment Industry, Dimethylphenylsilanol sodium salt, 97% is used as a surface treatment agent for materials such as glass, metal, and plastic. It provides enhanced adhesion and compatibility with other materials, allowing for better bonding and improved product performance.
Used in the Synthesis of Organosilicon Compounds:
Dimethylphenylsilanol sodium salt, 97% is utilized in the synthesis of various organosilicon compounds, which are used in the production of silicones, adhesives, and sealants. Its presence in these compounds contributes to the unique properties of these materials, such as their thermal stability, water resistance, and flexibility.

InChI:InChI=1/C8H11OSi.Na/c1-10(2,9)8-6-4-3-5-7-8;/h3-7H,1-2H3;/q-1;+1/rC8H11NaOSi/c1-11(2,10-9)8-6-4-3-5-7-8/h3-7H,1-2H3

Upstream product

• 5272-18-4 dimethylphenylsilanol 
• 768-33-2 phenyldimethylsilyl chloride 
• 56-33-7 1,1,3,3-tetramethyl-1,3-diphenyldisiloxane 
• 1825-58-7 dimethyl(ethoxy)phenylsilane 

Downstream Products

• 73703-38-5 bis(phenyldimethylsiloxy)methylsilane 
• 13360-20-8 (allyloxy)dimethylphenylsilane 
• 18758-83-3 3-(dimethyl-phenyl-silanyloxy)-1,1,5,5-tetramethyl-1,3,5-triphenyl-trisiloxane 
• 14920-92-4 pentamethyl(phenyl)disiloxane 
• 18848-30-1 1,1,5,5-tetramethyl-1,3,3,5-tetraphenyl-trisiloxane 
• 5272-18-4 dimethylphenylsilanol 
• 206128-80-5 (C₅H₅)Re(NO)(P(C₆H₅)3)(C(O)OSi(CH₃)2C₆H₅) 
• 192699-85-7 (η(5)-C5Me5)Re(CO)(NO)(COOSiMe2Ph) 
• 462-06-6 fluorobenzene 
• 73703-32-9 C₂₁H₃₄O₄Si₃ 

Relevant academic research and scientific papers

Synthesis and properties of ionic liquids with siloxane-functionalized cations

Four novel ionic liquids with siloxane-functionalized cations were synthesized and characterized. Their thermal stability was studied by the TG method; glass transition points, viscosities, and densities were also measured.

Preparation and characterization of the rhenium silyl esters (η5-C5Me5)(CO)(NO)ReC(O)OSiR3 (SiR3 = SiMe2Ph, SiEt3)

Three synthetic approaches to the rhenium silyl esters Cp * (CO)(NO)ReC(O)OSiEt3 (3) and Cp * (CO)(NO)ReC(O)OSiMe2Ph (4) were evaluated. (a) Treatment of a CH2Cl2 solution of Cp * (CO)2(NO)Re+BF-4 with a silanolate NaOSiEt3 (5) or NaOSiMe2Ph (6) provided 90% isolated yields of 3 and 4. These stable orange-yellow solids are extremely moisture sensitive: traces of water hydrolyze them to Cp * (CO)(NO)ReCO2H and the parent silanol. IR and NMR spectral data of 3 and 4 are consistent with nonchelating μ(η1-C:η1-O) metalloester structures. Less efficient preparative routes to 3 and 4 include treatment of (b) Cp * (CO)(NO)ReCO2H with the requisite chloroalkylsilane and NiPr2Et, and (c) Cp * (CO)(NO)ReCO-2Na+ (7Na+) with the chloroalkylsilane. The new rhenium CO2 adducts Cp * (CO)(NO)ReCO-2M+ (7Li+, 7Na+) were generated by deprotonation of Cp * (CO)(NO)ReCO2H with excess LiH or NaH THF suspensions at 0°C. Both 7Li+ and 7Na+ were characterized by their solution IR spectra and by the formation of their derivatives with silyl and tin chlorides.