Items 211 to 220 of 289 total
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Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
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N-(2,2,2-Trichloroethoxy)carbonyl] Nortilidine-d3 | 1246820-72-3 | sc-474870 | 1 mg | $480.00 | ||
N-(2,2,2-Trichloroethoxy)carbonyl] Nortilidine-d3 is an isotopically labeled compound that offers unique insights into reaction pathways and molecular interactions. The presence of deuterium enhances mass spectrometry resolution, enabling precise tracking of reaction intermediates. As an acid halide, it exhibits distinct reactivity patterns, facilitating acylation and providing a deeper understanding of electrophilic behavior in various biochemical contexts. Its isotopic labeling allows for innovative studies in metabolic tracing and kinetic analysis. | ||||||
Tridecanoic Acid Ethyl-d5 Ester | 28267-29-0 (unlabeled) | sc-474874 | 25 mg | $380.00 | ||
Tridecanoic Acid Ethyl-d5 Ester is an isotopically labeled compound that serves as a valuable tool for studying lipid metabolism and fatty acid pathways. The incorporation of deuterium enhances its detection in analytical techniques, allowing for detailed examination of metabolic flux and enzymatic activity. As an ester, it participates in unique hydrolysis and transesterification reactions, providing insights into reaction kinetics and molecular dynamics in biochemical systems. Its isotopic labeling aids in elucidating complex biochemical interactions. | ||||||
2-(5Z)-5-Tetradecen-1-yl-cyclobutanone-D17 | sc-474877 | 1 mg | $380.00 | |||
2-(5Z)-5-Tetradecen-1-yl-cyclobutanone-D17 is an isotopically labeled compound that facilitates the investigation of lipid signaling and metabolic pathways. The presence of deuterium allows for enhanced tracking in mass spectrometry, enabling researchers to dissect reaction mechanisms and metabolic fluxes with precision. Its unique cyclobutanone structure contributes to distinct reactivity patterns, influencing molecular interactions and stability in various biochemical environments. | ||||||
3-Tridecylhexadecanoic Acid Ethyl-d5 Ester | sc-474881 | 10 mg | $430.00 | |||
3-Tridecylhexadecanoic Acid Ethyl-d5 Ester is an isotopically labeled fatty acid derivative that serves as a valuable tool for studying lipid metabolism and cellular dynamics. The incorporation of deuterium enhances its detectability in analytical techniques, allowing for detailed exploration of lipid interactions and metabolic pathways. Its long-chain structure influences hydrophobic interactions and membrane fluidity, providing insights into lipid behavior in biological systems. | ||||||
Tridehydro Pirlimycin-d5 | sc-474903 | 1 mg | $480.00 | |||
Tridehydro Pirlimycin-d5 is an isotopically labeled compound that facilitates advanced studies in biochemical pathways and molecular interactions. The presence of deuterium allows for precise tracking in mass spectrometry, enhancing the understanding of reaction kinetics and metabolic processes. Its unique structural features may influence binding affinities and conformational dynamics, offering insights into the behavior of similar compounds in various biochemical environments. | ||||||
3,4,5-Trimethoxybenzyl-d9 Bromide | sc-474916 | 10 mg | $430.00 | |||
3,4,5-Trimethoxybenzyl-d9 Bromide is an isotopically labeled compound that serves as a valuable tool for probing molecular dynamics and interactions. The incorporation of deuterium enhances its detectability in spectroscopic analyses, allowing for detailed investigations into reaction mechanisms and pathways. Its distinct electronic properties and steric effects can influence reactivity and selectivity in chemical reactions, providing insights into the behavior of related aromatic compounds in diverse biochemical contexts. | ||||||
6,10,11-Triethylcarbonate Daunomycinone-13CD3 8-Formaldehyde | sc-474933 | 0.25 mg | $430.00 | |||
6,10,11-Triethylcarbonate Daunomycinone-13CD3 8-Formaldehyde is an isotopically labeled compound that facilitates advanced studies in metabolic pathways and molecular interactions. The presence of deuterium allows for enhanced resolution in NMR and mass spectrometry, enabling researchers to trace reaction kinetics with precision. Its unique structural features may influence hydrogen bonding and steric hindrance, providing insights into the behavior of similar carbonyl-containing compounds in various biochemical environments. | ||||||
Triethylenephosphoramide-d12 | 1246816-29-4 | sc-474937 | 1 mg | $360.00 | ||
Triethylenephosphoramide-d12 is an isotopically labeled compound that serves as a valuable tool for probing molecular dynamics and interactions in biochemical systems. The incorporation of deuterium enhances the sensitivity of spectroscopic techniques, allowing for detailed analysis of reaction mechanisms and pathways. Its distinct phosphoramidate structure may alter electronic properties and reactivity, influencing nucleophilic attack and coordination with metal ions, thus providing deeper insights into phosphorous chemistry in biological contexts. | ||||||
Triethylmelamine-d5 | 16268-92-1 (unlabeled) | sc-474941 | 2.5 mg | $380.00 | ||
Triethylmelamine-d5 is an isotopically labeled compound that facilitates advanced studies in molecular behavior and interactions. The presence of deuterium isotopes enhances NMR and mass spectrometry sensitivity, enabling precise tracking of metabolic pathways and reaction kinetics. Its unique structure may influence hydrogen bonding and steric effects, providing insights into the dynamics of amine interactions in various biochemical environments, thus enriching our understanding of nitrogen chemistry. | ||||||
D-Threonine-4-13C-4,4,4-d3 | 632-20-2 (unlabeled) | sc-474980 | 2.5 mg | $360.00 | ||
D-Threonine-4-13C-4,4,4-d3 is an isotopically labeled amino acid that serves as a powerful tool for metabolic tracing and biochemical analysis. The incorporation of carbon-13 and deuterium isotopes allows for enhanced resolution in NMR spectroscopy, aiding in the elucidation of metabolic flux and enzymatic pathways. Its distinct isotopic signature can influence reaction kinetics and substrate specificity, providing valuable insights into the role of threonine in various biochemical processes. |