"silicone fluid"
- 6 Items Found-
أحادي الهيدروجين المتخلص من البوليديميثيلسيلوكسان، غير متماثل (SOD-H101)
1,Polymer Matrix Single-terminal Silicone Graft Modification Utilizing the unique terminal silicon-hydrogen bond (Si-H) of asymmetric PDMS, directional hydrosilylation reaction with unsaturated double bonds and active hydroxyl sites of polymers such as polyether, acrylic resin, epoxy resin and ...
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المونوديهيدروكسي المنهى البوليديميثيلسيلوكسان، غير مقاس ((SOD-Q403)
1. Asymmetric Controlled Cross-linking Silicone Precursor This product is a special asymmetric hydroxyl-terminated polydimethylsiloxane with unique monodihydroxy differential reactive structure. Different from symmetric bifunctional silicone monomers, its asymmetric hydroxyl activity gradient ...
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مونوكاربينول أنهى بولي ثنائي ميثيل سيلوكسان غير متماثل (SOD-Q203)
1. Asymmetric Single-ended Reactive Modification Precursor This product is a high-performance asymmetric functional polydimethylsiloxane with single carbinol active terminal group and opposite inert silicone terminal. Different from traditional double-ended hydroxyl silicone, it features unilateral ...
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1,1,1,3,5,5،5-HEPTAMETHYL-3-[(TRIMETHYLSILYL) OXY]TRISILOXANE (رقم CAS 17928-28-8)
1. High-Purity Low-Viscosity Silicone Fluid Synthetic Precursor 1,1,1,3,5,5,5-Heptamethyl-3-[(trimethylsilyl)oxy]trisiloxane is a fully methyl-substituted branched trisiloxane with ultra-low viscosity, high structural symmetry and excellent molecular stability. The completely saturated inert methyl ...
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تريميثيل سيلانول (TMS) (رقم CAS 1066-40-6)
1. Key Hydrolytic Intermediate for High-Purity Silicone Polymer Synthesis Trimethylsilanol is the most fundamental hydroxyl-functionalized monosilane intermediate in the organosilicon industry, possessing a single reactive silicon hydroxyl group and stable fully methylated saturated skeleton. It can ...
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تريكلور ((6-فينيلهيكسيل) سيلان (CAS NO. 18035-33-1)
1. High-efficiency Silylation & Surface Grafting Reagent This product is a high-activity trifunctional chlorosilane containing long-chain phenylalkyl structure. The three reactive Si-Cl bonds can undergo rapid hydrolysis and condensation reactions with hydroxyl groups on inorganic substrate surfaces...
