Items 31 to 40 of 112 total
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
N-[23-(9-Mercaptononyl)-3,6,9,12,15,18,21-Heptaoxatricosanyl]-N′-(biotinyl)ethylenediamine | sc-224116 | 2.5 mg | $490.00 | |||
N-[23-(9-Mercaptononyl)-3,6,9,12,15,18,21-Heptaoxatricosanyl]-N'-(biotinyl)ethylenediamine exhibits remarkable properties in electronics due to its multifunctional structure. The presence of multiple ether linkages enhances solubility and facilitates self-assembly into organized nanostructures. Its thiol group promotes strong interactions with metal surfaces, enabling efficient charge transfer. Additionally, the biotinyl moiety allows for specific binding, potentially enhancing sensor sensitivity and selectivity. | ||||||
Etioporphyrin I | 448-71-5 | sc-263319 sc-263319A | 100 mg 1 g | $259.00 $1644.00 | ||
Etioporphyrin I stands out in electronics for its unique electronic properties and ability to form stable complexes with metal ions. Its planar structure facilitates effective π-π stacking interactions, enhancing charge mobility. The presence of nitrogen atoms in the macrocycle contributes to its electron-donating capabilities, which can improve conductivity. Furthermore, its ability to undergo redox reactions allows for tunable electronic characteristics, making it a candidate for advanced electronic applications. | ||||||
Diphenyliodonium nitrate | 722-56-5 | sc-255116 | 25 g | $169.00 | ||
Diphenyliodonium nitrate exhibits remarkable properties in electronics due to its ability to generate reactive intermediates upon photolysis. This compound facilitates rapid electron transfer processes, enhancing the efficiency of charge carriers in various materials. Its unique structure allows for strong dipole interactions, which can influence the alignment of adjacent molecules, optimizing charge transport. Additionally, its role as a photoinitiator in polymerization reactions underscores its significance in developing advanced electronic components. | ||||||
Phosphonitrilic chloride trimer | 940-71-6 | sc-255423 sc-255423A sc-255423B sc-255423C | 25 g 100 g 500 g 1 kg | $224.00 $427.00 $1700.00 $3200.00 | ||
Phosphonitrilic chloride trimer is notable in electronics for its unique polymeric structure, which promotes strong intermolecular interactions. This compound exhibits high thermal stability and can form robust networks, enhancing dielectric properties in insulating materials. Its reactivity as an acid halide allows for selective functionalization, enabling tailored modifications that improve conductivity and charge mobility. These characteristics make it a key player in the development of advanced electronic devices. | ||||||
Phenylphosphonic acid | 1571-33-1 | sc-236378 sc-236378A | 5 g 100 g | $27.00 $30.00 | ||
Phenylphosphonic acid stands out in electronics due to its ability to form stable complexes with metal ions, enhancing charge transfer processes. Its unique phosphonic acid group facilitates strong hydrogen bonding, which can improve the mechanical properties of polymer matrices. Additionally, its reactivity allows for the formation of phosphonate esters, which can modify surface properties and enhance adhesion in electronic components. These features contribute to its role in optimizing performance in various electronic applications. | ||||||
1-Hexadecanethiol | 2917-26-2 | sc-237565 | 500 mg | $212.00 | ||
1-Hexadecanethiol is notable in electronics for its ability to self-assemble into well-ordered monolayers on metal surfaces, enhancing conductivity and stability. The long hydrophobic alkyl chain promotes strong van der Waals interactions, while the thiol group forms robust bonds with metal substrates, improving surface functionalization. This unique behavior aids in the development of biosensors and electronic devices, optimizing interfacial properties and charge transport efficiency. | ||||||
Methyl 3-mercaptopropionate | 2935-90-2 | sc-255279 sc-255279A | 25 g 100 g | $50.00 $76.00 | ||
Methyl 3-mercaptopropionate exhibits intriguing properties in electronics due to its unique thiol group, which facilitates strong interactions with metal surfaces, enhancing adhesion and stability. Its flexible molecular structure allows for effective self-assembly, creating organized layers that improve electronic performance. The presence of the ester group contributes to its reactivity, enabling diverse chemical modifications that can tailor surface characteristics for specific electronic applications. | ||||||
Silicon | 7440-21-3 | sc-250977 | 50 g | $90.00 | ||
Silicon is a pivotal element in electronics, characterized by its semiconductor properties that enable efficient charge carrier mobility. Its crystalline structure allows for effective doping, which fine-tunes electrical conductivity. The formation of a native oxide layer enhances stability and passivation, while its ability to form covalent bonds facilitates integration with various materials. Silicon's unique bandgap properties are crucial for the development of transistors and photovoltaic cells, driving innovation in electronic devices. | ||||||
Selenium oxychloride | 7791-23-3 | sc-236873 | 10 g | $145.00 | ||
Selenium oxychloride exhibits unique properties as an acid halide, particularly in its role as a precursor in electronic materials. Its molecular interactions enable the formation of selenium-based thin films, which are essential for optoelectronic applications. The compound's reactivity with various substrates allows for tailored surface modifications, enhancing charge transport. Additionally, its ability to form stable complexes with metal ions can influence electronic properties, making it a versatile component in advanced electronic systems. | ||||||
Telluric acid | 7803-68-1 | sc-251110 | 25 g | $149.00 | ||
Telluric acid serves as a pivotal compound in electronics, particularly due to its ability to form tellurium-based nanostructures. Its strong acidity facilitates the synthesis of tellurium oxides, which exhibit semiconducting properties. The compound's unique molecular interactions promote the formation of stable tellurium bonds, enhancing conductivity and enabling precise doping in semiconductor materials. This versatility makes it integral in developing advanced electronic devices and materials. | ||||||