17905-99-6 Usage
Uses
Used in Silicone Polymer Synthesis:
TRIS(TRIMETHYLSILOXY)CHLOROSILANE is used as a coupling and crosslinking agent for the synthesis of silicone polymers, enhancing their properties and performance in various applications.
Used in Surface Modification Industry:
In the surface modification industry, TRIS(TRIMETHYLSILOXY)CHLOROSILANE is used as a surface modifier for glass, ceramic, and metal substrates. It improves the adhesion, durability, and other surface properties of these materials.
Used in Adhesives and Sealants Production:
TRIS(TRIMETHYLSILOXY)CHLOROSILANE is used as a precursor in the production of silicone rubber, adhesives, and sealants. It contributes to the development of high-performance adhesives and sealants with excellent bonding, flexibility, and resistance to environmental factors.
Used in Coatings Industry:
In the coatings industry, TRIS(TRIMETHYLSILOXY)CHLOROSILANE is used to formulate coatings with improved adhesion, durability, and resistance to chemicals, moisture, and temperature fluctuations.
Used in Electronics Industry:
TRIS(TRIMETHYLSILOXY)CHLOROSILANE is used in the electronics industry for the fabrication of encapsulants and potting compounds, providing protection to electronic components from environmental factors and mechanical stress.
Used in Textile Industry:
In the textile industry, TRIS(TRIMETHYLSILOXY)CHLOROSILANE is used to develop silicone-based softeners, water repellents, and other textile treatments, enhancing the performance and durability of fabrics.
Used in Cosmetics and Personal Care Industry:
TRIS(TRIMETHYLSILOXY)CHLOROSILANE is used in the cosmetics and personal care industry as a precursor for the production of silicone-based ingredients, such as emollients, conditioners, and skin protectants, which provide smoothness, softness, and moisture retention to the skin and hair.
Used in Medical Devices Industry:
In the medical devices industry, TRIS(TRIMETHYLSILOXY)CHLOROSILANE is used in the development of biocompatible materials and coatings for medical devices, improving their performance, durability, and patient safety.
Check Digit Verification of cas no
The CAS Registry Mumber 17905-99-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,9,0 and 5 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 17905-99:
(7*1)+(6*7)+(5*9)+(4*0)+(3*5)+(2*9)+(1*9)=136
136 % 10 = 6
So 17905-99-6 is a valid CAS Registry Number.
InChI:InChI=1/C9H27ClO3Si4/c1-14(2,3)11-17(10,12-15(4,5)6)13-16(7,8)9/h1-9H3
17905-99-6Relevant academic research and scientific papers
Utility of trichloroisocyanuric acid in the efficient chlorination of silicon hydrides
Varaprath, Sudarsanan,Stutts, Debra H.
, p. 1892 - 1897 (2007/10/03)
The potential of trichloroisocyanuric acid (TCCA) as a chlorination agent for efficient conversion of Si-H functional silanes and siloxanes to the corresponding Si-Cl functional moieties was explored. In comparison to methods using other chlorinating agents, TCCA is inexpensive, results in a much faster reaction and produces a high purity product with a conversion that is essentially quantitative. A variety of chloro derivatives of linear and cyclic structures have been synthesized from silicon hydrides using this reagent with impressive yields that typically exceed 90%: PhSiCl3 (97.5%); PhMeSiCl2 (95.5%); Ph3SiCl (97.5%); Vi3SiCl (98.7%); (EtO)3SiCl (99.7%); t-Bu3SiCl (～100%); (MeClSiO)4 (86.5%); (MeClSiO)5 (95%); (MeClSiO)7 (96.5%); Ph(OEt)2SiCl (98%); ClMe2SiOSiMe2Cl (98.6%); ClMe2SiOSiMeClOSiMe2Cl (94.6%); ClMe2Si(OSiMeCl)2OSiMe2C l (92.3%); (Me3SiO)3SiCl (97%); Me3SiOSiClPhOSiMe3 (99%); Me3SiO(SiMeClO)3SiMe3 (95.7%); ClSi(OSiMe3)2OSi(OSiMe3) 2Cl (93.6%). For monohydridosilanes, dichloromethane (CH2Cl2) was a suitable solvent in which nearly quantitative conversion was observed within several minutes following the addition of the silanes to TCCA. For certain cyclic and linear siloxanes, and especially silanes containing multiple hydrogen atoms on the same silicon for which the reaction is sluggish in CH2Cl2, tetrahydrofuran (THF) was the preferred solvent. For a sterically demanding silane that did not undergo chlorination even in THF viz., HSi(OSiMe3)2O-Si(OSiMe3)2H, 1,2-dichloroethane was the best solvent.
