Items 121 to 130 of 183 total
Display:
| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Felbamate-d4 | 106817-52-1 | sc-218465 | 5 mg | $398.00 | ||
Felbamate-d4 is a stable isotope-labeled variant of Felbamate, featuring deuterium substitutions that enhance its analytical traceability. The incorporation of deuterium alters the vibrational frequencies of molecular bonds, impacting reaction kinetics and thermodynamic properties. This modification allows for precise tracking in metabolic studies, revealing insights into molecular interactions and stability. Its distinct isotopic profile aids in elucidating complex biochemical pathways and enhancing the resolution of spectroscopic analyses. | ||||||
Granisetron-d3 | 109889-09-0 (unlabeled) | sc-280761 | 1 mg | $380.00 | ||
Granisetron-d3 is a stable isotope-labeled form of Granisetron, characterized by the incorporation of deuterium atoms. This substitution influences the molecule's vibrational modes, leading to unique isotopic effects that can alter reaction dynamics and enhance the specificity of analytical techniques. The presence of deuterium facilitates detailed studies of molecular interactions and pathways, providing a clearer understanding of kinetic behaviors and stability in various environments. | ||||||
Topotecan-d6 | 1044904-10-0 | sc-220273 | 1 mg | $380.00 | ||
Topotecan-d6 is a stable isotope-labeled variant of Topotecan, featuring deuterium substitutions that modify its molecular characteristics. These deuterium atoms enhance the compound's stability and alter its vibrational frequencies, which can influence reaction kinetics and thermodynamic properties. The isotopic labeling allows for precise tracking in complex systems, enabling researchers to investigate molecular interactions and pathways with greater accuracy and insight into its behavior in diverse chemical environments. | ||||||
rac Nebivolol-d4 (Major) | 138402-11-6 (unlabeled) | sc-219866 | 1 mg | $290.00 | ||
Rac Nebivolol-d4 (Major) is a stable isotope-labeled form of Nebivolol, distinguished by the incorporation of deuterium atoms. This modification affects its molecular dynamics, leading to altered rotational and vibrational modes that can influence reaction rates and mechanisms. The presence of deuterium enhances the compound's stability in various environments, facilitating detailed studies of its interactions and pathways in complex chemical systems, thereby providing deeper insights into its behavior. | ||||||
Candesartan-d5 | 1189650-58-5 | sc-217827 | 1 mg | $373.00 | ||
Candesartan-d5 is a stable isotope-labeled variant of Candesartan, featuring deuterium substitutions that modify its isotopic composition. This alteration influences its kinetic isotope effects, potentially affecting reaction pathways and rates in chemical processes. The presence of deuterium can enhance the stability of the compound in various conditions, allowing for precise tracking in metabolic studies and providing insights into molecular interactions and behavior in complex systems. | ||||||
Pemetrexed-d5 Disodium Salt | 150399-23-8 (unlabeled) | sc-219565 sc-219565A | 1 mg 10 mg | $338.00 $2800.00 | ||
Pemetrexed-d5 Disodium Salt is a stable isotope-labeled compound characterized by deuterium incorporation, which alters its isotopic signature. This modification can lead to unique reaction kinetics, influencing the rate and mechanism of chemical transformations. The presence of deuterium enhances the compound's stability, facilitating detailed studies of molecular interactions and dynamics in various environments, thereby offering insights into its behavior in complex chemical systems. | ||||||
Tamoxifen-ethyl-d5 | 157698-32-3 | sc-220186 | 1 mg | $330.00 | ||
Tamoxifen-ethyl-d5 is a stable isotope-labeled variant of Tamoxifen, featuring deuterium substitution that modifies its isotopic profile. This alteration can significantly impact its molecular interactions, particularly in hydrogen bonding and steric effects, leading to distinct reaction pathways. The deuterium incorporation enhances the compound's stability, allowing for precise tracking in kinetic studies and providing valuable insights into its behavior in diverse chemical environments and mechanisms. | ||||||
Dimethyl sulfoxide-d6 | 2206-27-1 | sc-257361 sc-257361A sc-257361B sc-257361C | 5 g 25 g 100 g 1 kg | $66.00 $158.00 $413.00 $4600.00 | 1 | |
Dimethyl sulfoxide-d6, a stable isotope variant, exhibits unique properties due to deuterium substitution, which influences its hydrogen bonding capabilities and solvent interactions. This modification enhances its role in studies of reaction kinetics, as the altered mass of deuterium affects the rate of isotopic exchange processes. Additionally, its distinct vibrational frequencies in infrared spectroscopy provide valuable insights into molecular conformations and solvation dynamics, enriching the understanding of solute-solvent interactions. | ||||||
Atrazine-d5 | 163165-75-1 | sc-217677 sc-217677A | 1 mg 10 mg | $292.00 $328.00 | ||
Atrazine-d5 is a stable isotope-labeled form of Atrazine, characterized by the incorporation of deuterium atoms. This modification influences its molecular dynamics, particularly in terms of vibrational frequencies and isotopic effects on reaction kinetics. The presence of deuterium alters the compound's interactions with enzymes and receptors, enabling enhanced specificity in studies of environmental fate and transport. Its unique isotopic signature facilitates advanced analytical techniques, providing deeper insights into its behavior in various chemical contexts. | ||||||
Coumarin-d4 | 185056-83-1 | sc-394031 | 5 mg | $440.00 | ||
Coumarin-d4 is a stable isotope-labeled variant of Coumarin, featuring deuterium substitutions that modify its spectral properties and molecular interactions. The incorporation of deuterium enhances its NMR characteristics, allowing for precise tracking in complex mixtures. This isotopic labeling influences reaction pathways and kinetics, providing insights into its behavior in photochemical processes. Its distinct isotopic profile aids in advanced analytical methodologies, enriching studies of its environmental and chemical dynamics. | ||||||