Items 1 to 10 of 112 total
Display:
Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
---|---|---|---|---|---|---|
11-Mercaptoundecanoic acid | 71310-21-9 | sc-251618 sc-251618A | 5 g 50 g | $97.00 $821.00 | 6 | |
11-Mercaptoundecanoic acid features a long hydrocarbon chain with a thiol group that imparts unique properties for electronic applications. Its ability to form self-assembled monolayers on metal surfaces enhances conductivity and stability. The thiol group facilitates strong metal-sulfur interactions, promoting effective charge transfer. Additionally, its amphiphilic nature allows for tailored surface modifications, optimizing electronic device performance through improved interface characteristics and reduced energy barriers. | ||||||
Triallyl Phosphate | 1623-19-4 | sc-489045 sc-489045A | 25 ml 100 ml | $258.00 $781.00 | ||
Triallyl Phosphate is a unique organophosphate compound characterized by its tri-allyl structure, which facilitates multiple pathways for reactivity. Its ability to engage in electrophilic interactions enhances its role in polymerization processes, particularly in the formation of cross-linked networks. The compound exhibits significant thermal stability and low viscosity, making it suitable for various electronic applications. Its distinct molecular interactions contribute to its effectiveness as a plasticizer and flame retardant in electronic materials. | ||||||
MOPS, Free Acid | 1132-61-2 | sc-216097 sc-216097A sc-216097B sc-216097C | 100 g 500 g 1 kg 5 kg | $46.00 $175.00 $226.00 $960.00 | 1 | |
MOPS, Free Acid, is characterized by its buffering capacity and pH stability, making it essential in electronic applications. Its unique structure allows for effective ionic interactions, enhancing solubility in aqueous environments. The acid's ability to form stable complexes with metal ions can influence charge transport properties, while its low viscosity aids in uniform dispersion within electronic materials. These features contribute to improved performance in various electrochemical systems. | ||||||
Selenium | 7782-49-2 | sc-250973 | 50 g | $61.00 | 1 | |
Selenium plays a pivotal role in electronics due to its semiconductor properties, enabling efficient charge carrier mobility. Its unique ability to form covalent bonds with other elements enhances its conductivity, making it ideal for photoconductive applications. Selenium's distinct crystal structure allows for anisotropic electrical properties, which can be exploited in photovoltaic cells. Additionally, its reactivity with halogens facilitates the formation of various compounds, broadening its utility in electronic devices. | ||||||
Biphenyl-4,4′-dithiol | 6954-27-4 | sc-252436 | 1 g | $320.00 | ||
Biphenyl-4,4'-dithiol exhibits remarkable properties in electronics, particularly due to its ability to form stable charge-transfer complexes. The presence of thiol groups enhances its electron-donating capacity, facilitating efficient charge transport in organic semiconductors. Its unique molecular structure allows for strong π-π stacking interactions, which improve conductivity and stability in thin-film applications. Additionally, the compound's reactivity with metal ions can lead to the formation of conductive metal-organic frameworks, expanding its potential in advanced electronic materials. | ||||||
L-Serine O-sulfate potassium salt | 17436-02-1 | sc-235478 | 25 mg | $229.00 | 3 | |
L-Serine O-sulfate potassium salt demonstrates intriguing properties in electronics, primarily through its ability to engage in ionic interactions that enhance conductivity. The sulfate group contributes to its solubility and facilitates charge mobility, making it suitable for use in electrochemical applications. Its unique molecular configuration allows for effective dipole-dipole interactions, which can improve the stability of electronic devices. Additionally, its reactivity with various substrates can lead to innovative pathways in material design. | ||||||
Mesoporphyrin IX dihydrochloride | 68938-72-7 | sc-235601 | 50 mg | $127.00 | 1 | |
Mesoporphyrin IX dihydrochloride exhibits remarkable characteristics in electronics, particularly due to its unique porphyrin structure that facilitates strong π-π stacking interactions. This arrangement enhances charge transfer efficiency, making it a candidate for organic semiconductors. Its ability to form stable complexes with metal ions can lead to tailored electronic properties, while its solubility in various solvents allows for versatile integration into electronic materials. The compound's distinct electronic states contribute to its potential in photonic applications. | ||||||
23-(9-Mercaptononyl)-3,6,9,12,15,18,21-Heptaoxatricosanoic Acid | 221222-49-7 | sc-216321 | 10 mg | $480.00 | ||
23-(9-Mercaptononyl)-3,6,9,12,15,18,21-Heptaoxatricosanoic Acid showcases intriguing properties in electronics, primarily due to its unique multi-oxime structure that promotes hydrogen bonding and dipole interactions. These features enhance its dielectric properties, making it suitable for capacitive applications. Additionally, its ability to form self-assembled monolayers can improve surface conductivity, while its tunable hydrophilicity allows for effective integration into various electronic substrates. | ||||||
3-Methyl-1-butanethiol | 541-31-1 | sc-231817 | 5 g | $65.00 | ||
3-Methyl-1-butanethiol exhibits notable characteristics in electronics, particularly through its thiol functional group, which facilitates strong nucleophilic interactions. This property enhances its reactivity in surface modification processes, allowing for the formation of robust metal-thiol bonds. Its unique steric configuration contributes to effective charge transport, while its volatility aids in vapor deposition techniques, making it a candidate for advanced electronic materials and sensor applications. | ||||||
Selenic acid solution | 7783-08-6 | sc-236872 sc-236872A | 25 ml 100 ml | $74.00 $253.00 | ||
Selenic acid solution is distinguished in electronics by its strong oxidizing properties, which enable it to facilitate the etching of semiconductor materials. Its ability to form selenate ions enhances surface reactivity, promoting effective adhesion in thin-film applications. The solution's high polarity and dipole moment contribute to its solvation dynamics, influencing charge carrier mobility. Additionally, its unique redox behavior allows for tailored electrochemical processes in device fabrication. |