Stable Isotopes
Items 51 to 60 of 183 total
Display:
| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Simvastatin-d6 Hydroxy Acid, Ammonium Salt | 139893-43-9 (unlabeled) | sc-220105 sc-220105A | 1 mg 10 mg | $403.00 $2249.00 | 1 | |
Simvastatin-d6 Hydroxy Acid, Ammonium Salt, as a stable isotope, features deuterium substitution that modifies its hydrogen bonding capabilities, leading to altered solubility and reactivity profiles. This isotopic variation enhances its spectroscopic signatures, allowing for detailed analysis of molecular interactions. The presence of deuterium can also influence reaction pathways and kinetics, providing insights into mechanistic studies and the behavior of similar compounds in complex systems. | ||||||
tert-Butan(ol-d) | 3972-25-6 | sc-258200 | 5 g | $51.00 | ||
tert-Butan(ol-d), as a stable isotope, exhibits intriguing behavior due to its deuterium labeling, which modifies its vibrational modes and alters intermolecular forces. This substitution can affect solvation dynamics and reactivity in chemical processes, leading to unique kinetic profiles. Its distinct isotopic mass also influences isotope effects in reactions, providing insights into transition state stabilization and molecular interactions in complex systems. | ||||||
Ethylene glycol-d6 | 15054-86-1 | sc-257518 | 5 g | $540.00 | ||
Ethylene glycol-d6, as a stable isotope, showcases unique properties stemming from its deuterium substitution, which enhances its hydrogen bonding capabilities. This modification can lead to altered thermodynamic stability and changes in solubility patterns. The presence of deuterium also affects the reaction kinetics, allowing for detailed studies of molecular dynamics and isotope effects in various chemical environments, thereby enriching our understanding of molecular interactions and pathways. | ||||||
Trazodone-d6 Hydrochloride | 1181578-71-1 | sc-220319 | 1 mg | $380.00 | ||
Trazodone-d6 Hydrochloride, as a stable isotope, features deuterium substitution that modifies its molecular vibrations, leading to distinctive spectroscopic characteristics. This alteration enhances its detection in analytical techniques, facilitating the study of molecular interactions and reaction kinetics. The presence of deuterium can influence hydrogen bonding and solvation dynamics, providing insights into the behavior of complex molecular systems and enhancing the understanding of its reactivity in various chemical environments. | ||||||
Prostaglandin F2α-d4 | 34210-11-2 | sc-205468 sc-205468A | 50 µg 100 µg | $51.00 $130.00 | ||
Prostaglandin F2α-d4, as a stable isotope, exhibits distinctive characteristics due to its deuterium labeling, which influences its molecular interactions and reactivity. The incorporation of deuterium alters the vibrational frequencies of the molecule, providing insights into conformational dynamics. This isotope can also facilitate the exploration of metabolic pathways and enzymatic mechanisms, enhancing the understanding of reaction kinetics and molecular behavior in complex biological systems. | ||||||
2-Aminodipyrido [1,2-a]imidazole-13C2,15N Hydrochloride | 175028-40-7 (unlabeled) | sc-358861 | 1 mg | $726.00 | ||
2-Aminodipyrido [1,2-a]imidazole-13C2,15N Hydrochloride, as a stable isotope, showcases unique isotopic labeling that affects its electronic properties and bonding interactions. The presence of carbon-13 and nitrogen-15 isotopes can modify the molecule's resonance structures, influencing its reactivity and stability in various chemical environments. This isotope serves as a valuable tool for tracing reaction pathways and studying molecular dynamics, providing deeper insights into its behavior in complex systems. | ||||||
Benzoic acid-d | 406679-59-2 | sc-319853 | 10 g | $265.00 | ||
Benzoic acid-d, as a stable isotope, features deuterium substitution that alters its vibrational modes and hydrogen bonding characteristics. This modification enhances its solubility and reactivity in specific solvents, impacting reaction kinetics and equilibrium constants. The presence of deuterium can also influence isotope effects in chemical reactions, making it a useful probe for studying mechanistic pathways and molecular interactions in various environments. | ||||||
3-Aminobiphenyl-d9 | 1020718-93-7 | sc-206621 | 2.5 mg | $430.00 | ||
3-Aminobiphenyl-d9, as a stable isotope, exhibits unique isotopic labeling that influences its electronic properties and molecular dynamics. The incorporation of deuterium alters the vibrational frequencies of the amino and biphenyl groups, affecting their reactivity and interaction with other molecules. This modification can lead to distinct kinetic isotope effects, providing insights into reaction mechanisms and facilitating the study of molecular conformations in complex systems. | ||||||
Pyridoxal-methyl-d3 | 1173023-49-8 | sc-391412 | 1 mg | $500.00 | ||
Pyridoxal-methyl-d3, a stable isotope, exhibits unique isotopic labeling that facilitates advanced analytical techniques, particularly in mass spectrometry. The incorporation of deuterium alters the vibrational frequencies, enhancing the resolution of spectral data. This isotope's distinct mass allows for precise tracking of metabolic pathways and interactions in complex biological systems. Its modified kinetic properties can influence reaction rates, providing insights into enzymatic mechanisms and molecular dynamics. | ||||||
Quetiapine-d8 Fumarate | 1185247-12-4 | sc-219685 | 1 mg | $377.00 | ||
Quetiapine-d8 Fumarate, as a stable isotope, exhibits distinctive properties due to its deuterium-enriched structure. This isotopic substitution can lead to altered vibrational frequencies, impacting molecular interactions and stability. The presence of deuterium enhances the precision of NMR spectroscopy, allowing for detailed analysis of conformational dynamics. Additionally, its unique isotopic signature aids in tracing metabolic pathways, providing insights into reaction mechanisms and molecular behavior in complex systems. | ||||||