"liquid silicone lubricant"
- 15 Items Found-
1,1,1,3,5,5,5-ヘプタメチル−3−[TRIMETHYLSILYL) OXY]TRISILOXANE (CAS番号 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 siloxane skeleton eliminates active reactive groups, providing outstanding thermal stability, low volatility and low surface tension characteristics. It can be used as a high
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1"""""""""1,5,5-テトラメチル-3,3-ディフェニル-1,5-トリシロキサンデリル) DI-3,1-プロパネディリル]2-メチル-2-プロペノアート (CAS番号1581235-15-5)
1. High-temperature Resistant Silicone Polymer Intermediate This diphenyl trisiloxane monomer features rigid phenyl side groups and stable Si-O-Si backbone, possessing excellent high-temperature thermal stability and low-temperature toughness. It serves as a key structural intermediate for synthesizing high-performance phenyl-modified silicone resins and silicone rubbers, effectively improving the thermal oxidation resistance and service temperature range of silicone polymers
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デメチル-N-オクチルクロロシラン (CAS番号18162-84-0)
1. Linear Alkyl Modified Silicone Synthetic Monomer This product is a high-activity monofunctional alkyl chlorosilane with linear n-octyl and dimethyl composite alkyl structure. It can undergo controllable hydrolysis and graft copolymerization to introduce straight-chain octyl hydrophobic segments into silicone molecular chains. It effectively optimizes the surface lipophilicity, molecular chain flexibility and low-temperature fluidity of conventional dimethyl silicone
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モノビニール末端ポリダイメチルシロキサン,アシメトリック (SOD-V102)
1. Asymmetric Single-ended Addition Curing Modifier This product is a high-performance asymmetric functional polydimethylsiloxane with single terminal vinyl active group and opposite inert silicone structure. It features unilateral hydrosilylation reactivity without full cross-linking network restriction. It can undergo precise addition curing reaction with hydrogen-containing silicone monomers, enabling directional grafting modification. It effectively avoids excessive cross
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トリクロロオクタデシルシラン
(CAS NO.112 -04 -9) 1. Long-chain Alkyl Silicone Polymer Synthetic Monomer This product is a high-activity trifunctional long-chain alkyl chlorosilane with three hydrolyzable Si-Cl reactive sites and stable saturated octadecyl linear alkyl segments. It can undergo uniform hydrolysis and polycondensation reaction to synthesize high-stability long-chain alkyl modified silicone resin and polysiloxane polymers. It effectively improves the lipophilicity, film-forming property and
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モノヒドリド・ターミネートポリダイメチルシロキサン,非対称 (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 polyurethane is carried out under platinum catalysis to realize controllable single-terminal grafting of PDMS segments. It effectively avoids system curing, thickening and gelation
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モノカルビノール ポリダイメチルシロキサン ASYMMETRIC ((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 controllable reaction activity and no cross-linking saturation limitation. It can perform selective grafting and chain extension reaction with isocyanate, anhydride and carboxyl
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クロロジメチルプロピルシラン [ジメチルプロピルシリレーティング剤] (CAS No.17477-29-1)
1. Professional Dimethylpropylsilylating Reagent This product is a high-activity monofunctional alkyl chlorosilane specially used for dimethylpropylsilylation modification. The reactive silicon-chlorine bond can efficiently react with active hydrogen groups such as hydroxyl and carboxyl under mild conditions to complete selective silylation derivatization. It features stable grafting structure, low steric hindrance and high reaction controllability, which is widely used in
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BIS ((METHACRYLOXY) BUTYLPOLYDIMETHYLSILOXANE ((SOT-J305)) 試料の種類について
1. UV-curable Silicone Modified Monomer This product is a high-performance bifunctional active silicone polymer containing terminal methacryloxy unsaturated double bonds and flexible PDMS backbone. The terminal methacrylate groups possess excellent UV curing activity and free radical polymerization reactivity. It can be copolymerized and cross-linked with acrylic monomers under light initiation conditions, serving as a core functional monomer for synthesizing UV-curable
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1,1,5,5-テトラメチル-3,3-ディフェニルトリシロキサン (CAS No.17875-55-7)
1. High and Low Temperature Resistant Silicone Resin Modification This product is a typical diphenyl trisiloxane functional monomer with stable Si-O-Si backbone and rigid biphenyl structural units. It can be introduced into silicone resin and silicone rubber molecular chains to effectively improve high-temperature thermal oxidation stability and low-temperature flexibility of conventional dimethyl silicone materials, expanding the extreme temperature service range of silicone
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デメチロクタデチルクロロシラン (CAS No.18643-08-8)
1. Long-chain Alkyl Modified Silicone Synthetic Monomer This product is a high-activity monofunctional alkyl chlorosilane composed of dimethyl short-chain alkyl and long-chain octadecyl saturated alkyl structure. It can undergo controllable hydrolysis and grafting polymerization to introduce long hydrophobic alkyl segments into silicone molecular chains. It effectively optimizes the surface lipophilicity, molecular flexibility and low-temperature resistance of traditional
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クロロジオボチロクタデシルシラン (CAS No.162578-86-1)
1. Long-chain Alkyl Modified Silicone Monomer This product is a high-performance monofunctional alkyl chlorosilane containing dual isobutyl branched chains and long-chain octadecyl linear alkyl structure. With high reactive Si-Cl bond activity, it can undergo hydrolysis and polycondensation to introduce composite branched-linear alkyl segments into silicone molecular chains. It effectively improves the lipophilicity, molecular chain flexibility and low-temperature ductility