Items 1 to 10 of 381 total
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Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
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Potassium silicate, anhydrous | 1312-76-1 | sc-272105 | 100 g | $37.00 | ||
Potassium silicate, anhydrous, is a versatile silicon compound known for its unique structural properties and reactivity. Its anhydrous form facilitates rapid dissolution in water, leading to the formation of silicate ions that can engage in various polymerization reactions. The compound exhibits strong ionic interactions, enhancing its stability and solubility in alkaline environments. Its ability to form silicate networks contributes to its role in modifying surface properties and influencing reaction kinetics in silicate-based systems. | ||||||
Trivinylmethylsilane | 18244-95-6 | sc-272754 | 1 g | $64.00 | ||
Trivinylmethylsilane is a silicon compound characterized by its unique vinyl groups, which enhance its reactivity in polymerization processes. The presence of these vinyl functionalities allows for efficient cross-linking and the formation of complex siloxane networks. This compound exhibits distinct thermal stability and can participate in hydrosilylation reactions, facilitating the incorporation of various functional groups. Its molecular structure promotes specific interactions that influence the kinetics of silane-based reactions, making it a key player in silicone chemistry. | ||||||
Silicon dioxide | 14808-60-7 | sc-203376 sc-203376A sc-203376B | 100 g 500 g 1 kg | $80.00 $100.00 $155.00 | ||
Silicon dioxide, a prominent silicon compound, exhibits a robust network structure that contributes to its exceptional hardness and chemical inertness. Its extensive hydrogen bonding and van der Waals interactions enhance its stability and influence its reactivity in various environments. As a key component in glass and ceramics, it plays a crucial role in determining physical properties like transparency and thermal resistance. Its unique surface characteristics also facilitate adsorption processes, impacting material interactions. | ||||||
Bis[3-(trimethoxysilyl)propyl]amine | 82985-35-1 | sc-239378A sc-239378 sc-239378B sc-239378C sc-239378D | 25 g 50 g 500 g 1 kg 5 kg | $31.00 $55.00 $510.00 $918.00 $2550.00 | ||
Bis[3-(trimethoxysilyl)propyl]amine is a versatile silicon compound characterized by its dual functionality, featuring both amine and silane groups. This structure enables strong covalent bonding with various substrates, enhancing adhesion and promoting cross-linking in polymer matrices. Its trimethoxysilyl groups facilitate hydrolysis, leading to siloxane bond formation, which significantly influences reaction kinetics. The compound's ability to form stable silane networks contributes to improved mechanical properties and durability in composite materials. | ||||||
1,3,5-Tris[(3,3,3-trifluoropropyl)methyl]cyclotrisiloxane | 2374-14-3 | sc-258948 sc-258948A | 5 g 25 g | $90.00 $270.00 | ||
1,3,5-Tris[(3,3,3-trifluoropropyl)methyl]cyclotrisiloxane is a unique silicon compound distinguished by its trifluoropropyl substituents, which impart exceptional hydrophobicity and chemical stability. The presence of multiple siloxane linkages enhances its ability to form robust networks, facilitating unique molecular interactions. Its distinct structure allows for tailored surface modifications, influencing adhesion properties and thermal resistance, making it suitable for specialized applications in materials science. | ||||||
n-Hexyltrimethoxysilane | 3069-19-0 | sc-269848 | 5 g | $24.00 | ||
n-Hexyltrimethoxysilane is a versatile silicon compound characterized by its long alkyl chain, which enhances its compatibility with organic materials. The trimethoxysilane groups facilitate hydrolysis and condensation reactions, promoting silane bonding to various substrates. This compound exhibits unique surface-active properties, improving wetting and adhesion. Its ability to form siloxane networks contributes to enhanced durability and resistance to environmental factors, making it significant in surface treatment applications. | ||||||
(Triethoxysilyl)cyclohexane | 18151-84-3 | sc-229567 | 5 g | $170.00 | ||
(Triethoxysilyl)cyclohexane is a unique silicon compound featuring a cyclohexane ring that imparts rigidity and steric hindrance, influencing its reactivity. The triethoxysilyl groups enable efficient hydrolysis, leading to the formation of siloxane bonds with substrates. This compound exhibits distinct hydrophobic characteristics, enhancing its compatibility with non-polar surfaces. Its molecular structure allows for tailored interactions in polymer matrices, promoting stability and enhancing mechanical properties in composite materials. | ||||||
Silicon carbide | 409-21-2 | sc-272454 | 500 g | $43.00 | ||
Silicon carbide is a remarkable silicon compound characterized by its strong covalent bonding and exceptional hardness. Its unique crystal structure facilitates diverse electronic and thermal properties, making it an excellent semiconductor. The compound exhibits high thermal conductivity and resistance to oxidation, which influences its reactivity in high-temperature environments. Additionally, its surface chemistry allows for effective functionalization, enhancing its interactions in various material systems. | ||||||
(Heptafluoropropyl)trimethylsilane | 3834-42-2 | sc-252877 | 1 g | $59.00 | ||
(Heptafluoropropyl)trimethylsilane is a distinctive silicon compound known for its unique fluorinated structure, which imparts exceptional hydrophobicity and low surface energy. This compound exhibits strong Si-C and Si-F bonds, influencing its reactivity and stability in various chemical environments. Its ability to form self-assembled monolayers enhances surface modification processes, while its distinct molecular interactions facilitate unique pathways in organosilicon chemistry, promoting diverse applications in material science. | ||||||
2-(4-Chlorosulfonylphenyl)ethyltrimethoxysilane | 126519-89-9 | sc-282650 sc-282650A | 5 g 25 g | $240.00 $357.00 | ||
2-(4-Chlorosulfonylphenyl)ethyltrimethoxysilane is a notable silicon compound characterized by its sulfonyl and trimethoxysilane functionalities. The presence of the chlorosulfonyl group enhances its reactivity, enabling efficient nucleophilic substitution reactions. This compound exhibits strong interactions with polar solvents, promoting adhesion and cross-linking in polymer matrices. Its unique molecular architecture facilitates the formation of siloxane networks, contributing to enhanced mechanical properties in composite materials. |