Items 231 to 240 of 381 total
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Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
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Allyltrimethoxysilane | 2551-83-9 | sc-239213 | 5 ml | $40.00 | ||
Allyltrimethoxysilane is a silicon compound characterized by its ability to form robust siloxane networks through its reactive allyl group. This compound exhibits unique reactivity due to the presence of methoxy groups, which enhance its nucleophilicity and facilitate cross-linking in polymer matrices. Its distinct molecular structure allows for selective interactions with various substrates, promoting efficient coupling reactions and enhancing material properties in silane-based formulations. | ||||||
Sodium metasilicate nonahydrate | 13517-24-3 | sc-251033 | 500 g | $159.00 | ||
Sodium metasilicate nonahydrate is a silicon compound notable for its high solubility in water, which facilitates the formation of silicate anions in solution. This compound exhibits unique properties such as strong alkalinity and the ability to act as a buffering agent, influencing reaction kinetics in various chemical processes. Its crystalline structure contributes to its stability and reactivity, enabling it to participate in hydrolysis and condensation reactions, which are essential in silicate chemistry. | ||||||
Octamethylcyclotetrasiloxane | 556-67-2 | sc-250610 | 25 g | $58.00 | ||
Octamethylcyclotetrasiloxane is a cyclic siloxane characterized by its unique ring structure, which allows for flexible molecular interactions and low viscosity. This compound exhibits distinct thermal stability and hydrophobic properties, making it an effective lubricant and surface modifier. Its ability to undergo dynamic equilibrium between cyclic and linear forms enhances its reactivity in polymerization processes, influencing the synthesis of silicone-based materials. | ||||||
(tert-Butyldimethylsilyloxy)acetaldehyde | 102191-92-4 | sc-253647 | 1 g | $128.00 | ||
(tert-Butyldimethylsilyloxy)acetaldehyde is a silicon compound notable for its unique silyl ether functionality, which enhances its reactivity in nucleophilic substitution reactions. The presence of the tert-butyl group provides steric hindrance, influencing reaction kinetics and selectivity. This compound can participate in various condensation reactions, facilitating the formation of complex siloxane networks. Its distinctive molecular structure contributes to its role in modifying surface properties and enhancing adhesion in polymer systems. | ||||||
Platinum(0)-1,3-divinyl-1,1,3,3-tetramethyldisiloxane complex solution | 68478-92-2 | sc-253281 | 5 g | $181.00 | ||
Platinum(0)-1,3-divinyl-1,1,3,3-tetramethyldisiloxane complex solution exhibits remarkable catalytic properties due to its unique platinum coordination with siloxane moieties. This interaction facilitates efficient cross-linking and polymerization processes, enhancing the formation of siloxane networks. The compound's dual vinyl and siloxane functionalities enable versatile reactivity, promoting distinct pathways in organosilicon chemistry. Its stability and reactivity profile make it a key player in advancing silicon-based materials. | ||||||
3-(Acryloyloxy)propyltrimethoxysilane | 4369-14-6 | sc-356617 sc-356617A | 5 g 25 g | $95.00 $328.00 | ||
3-(Acryloyloxy)propyltrimethoxysilane is a versatile silane compound characterized by its ability to form strong covalent bonds with various substrates through its acryloyloxy group. This functionality allows for efficient grafting onto surfaces, enhancing adhesion and compatibility in composite materials. The compound's trimethoxysilane groups facilitate hydrolysis and condensation reactions, promoting the formation of siloxane networks. Its unique reactivity and molecular structure enable tailored modifications in silicon chemistry, making it a significant contributor to material science advancements. | ||||||
Diphenyldifluorosilane | 312-40-3 | sc-285451 sc-285451A | 25 g 100 g | $173.00 $421.00 | ||
Diphenyldifluorosilane is a distinctive silicon compound known for its unique reactivity and molecular interactions. The presence of fluorine atoms enhances its electrophilic character, facilitating nucleophilic attack in various chemical pathways. This compound exhibits notable stability under certain conditions, allowing for selective reactions that can lead to the formation of siloxane bonds. Its diphenyl groups contribute to its hydrophobic nature, influencing surface properties and interactions in silicon-based materials. | ||||||
tert-Butyl(chloro)diphenylsilane | 58479-61-1 | sc-397881 | 2 g | $20.00 | ||
tert-Butyl(chloro)diphenylsilane is a silicon compound notable for its unique steric and electronic properties. The tert-butyl group imparts significant steric hindrance, influencing the reactivity of the silicon center and modulating its interactions with nucleophiles. This compound exhibits distinct pathways in cross-coupling reactions, where its chlorinated structure enhances reactivity. Additionally, its diphenyl moiety contributes to unique π-π stacking interactions, affecting solubility and stability in various media. | ||||||
3-Benzyloxy[6-[2-(tert-Butyldimethylsilyloxy)ethyl]methylamino]pyridine | 1076198-95-2 | sc-460317 | 100 mg | $300.00 | ||
3-Benzyloxy[6-[2-(tert-Butyldimethylsilyloxy)ethyl]methylamino]pyridine is a silicon compound characterized by its intricate molecular architecture, which promotes unique steric and electronic interactions. The tert-butyldimethylsilyloxy group enhances its solubility and stability, allowing for selective reactivity in diverse chemical environments. This compound's ability to engage in hydrogen bonding and π-π stacking interactions contributes to its distinctive behavior in silicon-based systems, influencing reaction kinetics and pathways. | ||||||
Hexamethyldisiloxane (analytical grade) | 107-46-0 | sc-250106 sc-250106A | 25 ml 100 ml | $17.00 $20.00 | ||
Hexamethyldisiloxane is a silicon compound notable for its unique siloxane backbone, which imparts flexibility and low surface tension. This compound exhibits remarkable hydrophobic properties, facilitating interactions with nonpolar solvents. Its structure allows for effective chain mobility, influencing viscosity and thermal stability. Additionally, the presence of silicon-oxygen bonds enhances its reactivity in condensation reactions, making it a versatile component in various silicon-based applications. |