Items 201 to 210 of 223 total
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Triticonazole | 131983-72-7 | sc-204929 sc-204929A | 5 g 10 g | $138.00 $199.00 | ||
Triticonazole serves as an analytical standard characterized by its ability to engage in specific molecular interactions that facilitate the study of enzymatic pathways. Its unique structural features promote selective binding to target enzymes, allowing for detailed kinetic analysis. The compound's stability across a range of conditions enhances its reliability in analytical applications, while its distinct physicochemical properties enable comprehensive investigations into its reactivity and interaction profiles in various environments. | ||||||
Chromoionophore II | 136499-31-5 | sc-239550 sc-239550A | 10 mg 25 mg | $251.00 $510.00 | ||
Chromoionophore II is an analytical standard notable for its unique ability to selectively bind cations, enabling precise ion-selective measurements. Its distinct molecular architecture allows for efficient electron transfer processes, which are crucial in electrochemical applications. The compound exhibits remarkable photophysical properties, including fluorescence, that facilitate real-time monitoring of ion concentrations. Additionally, its stability under varying pH conditions makes it a reliable tool for studying ion transport mechanisms. | ||||||
Robenidine-d8 hydrochloride | 1173097-77-2 | sc-301699 | 10 mg | $288.00 | ||
Robenidine-d8 hydrochloride serves as a valuable analytical standard, distinguished by its isotopic labeling that enhances mass spectrometric analysis. This compound exhibits unique interactions with various analytes, allowing for improved specificity in detection. Its stable isotopic composition aids in the elucidation of reaction pathways and kinetics, providing insights into molecular behavior. Furthermore, its solubility characteristics facilitate diverse analytical applications, making it a versatile tool in chemical analysis. | ||||||
tert-Butanol | 75-65-0 | sc-251126B sc-251126 sc-251126A | 50 ml 500 ml 1 L | $41.00 $51.00 $68.00 | ||
tert-Butanol is a notable analytical standard characterized by its ability to engage in hydrogen bonding, which influences solvation dynamics and enhances chromatographic separation. Its unique steric hindrance affects reaction kinetics, allowing for the study of nucleophilic substitution mechanisms. Additionally, its high polarity and low viscosity contribute to its effectiveness in various analytical techniques, providing reliable calibration and improving the accuracy of quantitative analyses. | ||||||
cis-1,2-Dichloroethene | 156-59-2 | sc-257247 | 1 g | $39.00 | ||
Cis-1,2-Dichloroethene serves as a valuable analytical standard due to its distinct geometric configuration, which influences its reactivity and interaction with various solvents. The presence of chlorine atoms introduces significant dipole moments, enhancing its solubility in polar solvents. Its unique electronic structure facilitates specific reaction pathways, making it useful for studying electrophilic addition reactions. Additionally, its volatility and density characteristics aid in precise analytical measurements, ensuring reliable data in various applications. | ||||||
Indeno[1,2,3-cd]fluoranthene | 193-43-1 | sc-235356 | 20 mg | $415.00 | ||
Indeno[1,2,3-cd]fluoranthene is a polycyclic aromatic hydrocarbon that serves as an analytical standard, notable for its planar structure and strong π-π stacking interactions. These interactions enhance its stability and influence its behavior in chromatographic separations. Its distinct fluorescence properties allow for sensitive detection in analytical methods, while its hydrophobic nature affects solubility in organic solvents, making it a key compound for studying environmental samples and complex mixtures. | ||||||
Benzo[ghi]fluoranthene | 203-12-3 | sc-233952 | 100 mg | $1300.00 | ||
Benzo[ghi]fluoranthene is a polycyclic aromatic hydrocarbon recognized as an analytical standard, characterized by its unique electronic structure that facilitates electron transfer processes. Its rigid, fused-ring system promotes significant intermolecular interactions, impacting its adsorption characteristics in various analytical techniques. Additionally, its distinct spectral properties enable precise quantification in complex matrices, while its low volatility aids in stability during storage and analysis. | ||||||
Oxydemeton-methyl | 301-12-2 | sc-257950 | 50 mg | $294.00 | 1 | |
Oxydemeton-methyl serves as a critical analytical standard, notable for its unique reactivity and interaction with nucleophiles. Its structure allows for specific binding with target analytes, enhancing detection sensitivity in chromatographic methods. The compound exhibits distinct spectral features, facilitating accurate identification and quantification. Furthermore, its stability under various conditions ensures reliable performance in analytical applications, making it a valuable reference material for environmental monitoring. | ||||||
Formononetin | 485-72-3 | sc-202614 | 5 mg | $122.00 | 2 | |
Formononetin is an important analytical standard characterized by its ability to form stable complexes with metal ions, which can influence its reactivity in various analytical techniques. Its distinct UV-Vis absorption spectrum aids in precise quantification, while its solubility in organic solvents enhances its versatility in different analytical matrices. Additionally, the compound's unique structural features allow for selective interactions in chromatographic separations, improving resolution and accuracy in analytical assessments. | ||||||
β-Tocotrienol | 490-23-3 | sc-358854 | 100 mg | $2765.00 | ||
β-Tocotrienol serves as a vital analytical standard, notable for its unique antioxidant properties that facilitate the study of lipid peroxidation processes. Its distinct fluorescence characteristics enable sensitive detection in various assays, while its hydrophobic nature influences partitioning behavior in chromatographic techniques. The compound's ability to interact with cellular membranes provides insights into membrane dynamics, enhancing the understanding of lipid interactions in analytical contexts. | ||||||