Items 81 to 90 of 112 total
Display:
| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
1-Pentadecanethiol | 25276-70-4 | sc-396836 | 1 g | $113.00 | ||
1-Pentadecanethiol is a significant compound in electronics, known for its ability to form robust self-assembled monolayers that enhance the stability and performance of electronic interfaces. Its long hydrocarbon chain contributes to hydrophobic interactions, optimizing surface energy and reducing noise in electronic components. The compound's thiol group enables strong binding to metal substrates, facilitating efficient electron transport and improving the reliability of nanoscale electronic devices. | ||||||
1-Undecanethiol | 5332-52-5 | sc-396838 | 5 g | $83.00 | ||
1-Undecanethiol plays a crucial role in electronics through its capacity to create highly ordered self-assembled monolayers, which improve the electrical properties of surfaces. The unique structure of its alkyl chain promotes effective van der Waals interactions, enhancing the mechanical stability of electronic components. Additionally, the thiol functional group allows for selective adsorption on metal surfaces, fostering enhanced charge transfer and minimizing interfacial resistance in nanoscale applications. | ||||||
Lithium difluoro(oxalato)borate | 409071-16-5 | sc-396975 | 25 g | $223.00 | ||
Lithium difluoro(oxalato)borate is notable in electronics for its exceptional ionic conductivity and electrochemical stability, making it an ideal electrolyte in advanced battery systems. Its unique coordination chemistry facilitates strong interactions with lithium ions, promoting efficient ion transport. The compound's ability to form stable complexes enhances its performance under varying temperatures, while its low viscosity contributes to improved ion mobility, crucial for high-performance energy storage solutions. | ||||||
(4-Phenoxyphenyl)diphenylsulfonium triflate | 240482-96-6 | sc-396963 | 1 g | $102.00 | ||
(4-Phenoxyphenyl)diphenylsulfonium triflate stands out in electronics due to its excellent photoinitiating properties, enabling rapid polymerization processes in photoresist applications. Its unique sulfonium structure allows for efficient charge transfer, enhancing the curing speed under UV light. The compound exhibits remarkable thermal stability, which is essential for maintaining performance in high-temperature environments. Additionally, its ability to generate reactive species upon irradiation facilitates precise patterning in microfabrication. | ||||||
(4-Phenylthiophenyl)diphenylsulfonium triflate | 111281-12-0 | sc-396964 | 1 g | $70.00 | ||
(4-Phenylthiophenyl)diphenylsulfonium triflate is notable in electronics for its exceptional electron-donating capabilities, which enhance conductivity in various applications. The compound's unique thiophenyl moiety contributes to its strong intermolecular interactions, promoting effective charge transport. Its high reactivity under UV light leads to rapid cross-linking in polymer matrices, making it ideal for advanced lithographic techniques. Furthermore, its stability under operational stress ensures reliable performance in demanding electronic environments. | ||||||
Germanium(II) telluride | 12025-39-7 | sc-397412 | 5 g | $136.00 | ||
Germanium(II) telluride is recognized in electronics for its intriguing semiconducting properties, particularly its narrow bandgap, which facilitates efficient charge carrier mobility. The compound exhibits strong covalent bonding between germanium and tellurium, leading to unique lattice dynamics that enhance thermal stability. Its anisotropic electrical conductivity allows for tailored electronic applications, while its ability to form heterostructures opens pathways for innovative device architectures. | ||||||
Poly(vinylidene fluoride) | 24937-79-9 | sc-264080 sc-264080A | 25 g 100 g | $31.00 $87.00 | ||
Poly(vinylidene fluoride) is a versatile polymer renowned for its piezoelectric and ferroelectric properties, which arise from its highly polar molecular structure. This polarity facilitates strong dipole interactions, enabling efficient energy conversion in sensors and actuators. Its crystalline phases exhibit distinct dielectric behaviors, allowing for tailored capacitance in electronic components. Additionally, the polymer's excellent thermal stability and mechanical strength enhance its performance in demanding electronic environments. | ||||||
12-Mercaptododecylphosphonic acid | 159239-33-5 | sc-396978 | 250 mg | $139.00 | ||
12-Mercaptododecylphosphonic acid is notable in electronics for its ability to form self-assembled monolayers, which enhance surface properties and improve adhesion in various substrates. The presence of the phosphonic acid group facilitates strong interactions with metal oxides, promoting effective passivation. Its long hydrocarbon chain contributes to hydrophobicity, while the thiol group enables robust bonding with metallic surfaces, optimizing electronic interfaces and enhancing device performance. | ||||||
8-Amino-1-octanethiol hydrochloride | 937706-44-0 | sc-396979 | 250 mg | $415.00 | ||
8-Amino-1-octanethiol hydrochloride exhibits unique properties in electronics through its ability to form stable thiol-metal bonds, enhancing the conductivity of metal surfaces. The amino group introduces polar interactions, which can modify surface charge and improve electron transfer rates. Its octane chain provides hydrophobic characteristics, while the hydrochloride form ensures solubility in various solvents, facilitating the creation of tailored nanostructures for advanced electronic applications. | ||||||
Bis(4-tert-butylphenyl)iodonium triflate | 84563-54-2 | sc-396952 sc-396952A sc-396952B sc-396952C | 1 g 5 g 100 g 500 g | $240.00 $500.00 $5000.00 $24000.00 | ||
Bis(4-tert-butylphenyl)iodonium triflate serves as a potent photoinitiator in electronic applications, exhibiting rapid decomposition under UV light to generate reactive radicals. Its bulky tert-butyl groups enhance solubility and reduce aggregation, promoting uniform polymerization in photoresists. The triflate counterion contributes to its stability and facilitates ionic interactions, optimizing charge transport in electronic materials. This compound's unique reactivity and structural features enable precise control over polymer network formation, crucial for advanced electronic devices. | ||||||