AAMA-d3, or 2-Amino-2-methyl-1-propanol-d3, is a deuterated derivative of 2-amino-2-methyl-1-propanol, which is an amino alcohol. This compound is characterized by the presence of a hydroxyl group (-OH) and an amino group (-NH2) attached to a branched carbon chain. The deuteration indicates that certain hydrogen atoms in the molecule have been replaced with deuterium, a stable isotope of hydrogen, which can be useful in various analytical techniques, including NMR spectroscopy. AAMA-d3 is typically utilized in research and development, particularly in studies involving metabolic pathways or as a tracer in chemical reactions. Its properties include being a colorless liquid with potential solubility in water and organic solvents, depending on the specific conditions. As with many amino alcohols, it may exhibit basicity due to the amino group and can participate in various chemical reactions, including those involving nucleophilic substitution or condensation. Safety data should be consulted for handling and storage, as with any chemical substance.

AAMA-d3

1795786-57-0: AAMA-d3, or 2-Amino-2-methyl-1-propanol-d3, is a deuterated derivative of 2-amino-2-methyl-1-propanol, which is an amino alcohol. This compound is characterized by the presence of a hydroxyl group (-OH) and an amino group (-NH2) attached to a branched carbon chain. The deuteration indicates that certain hydrogen atoms in the molecule have been replaced with deuterium, a stable isotope of hydrogen, which can be useful in various analytical techniques, including NMR spectroscopy. AAMA-d3 is typically utilized in research and development, particularly in studies involving metabolic pathways or as a tracer in chemical reactions. Its properties include being a colorless liquid with potential solubility in water and organic solvents, depending on the specific conditions. As with many amino alcohols, it may exhibit basicity due to the amino group and can participate in various chemical reactions, including those involving nucleophilic substitution or condensation. Safety data should be consulted for handling and storage, as with any chemical substance.

Stability Hygroscopic Applications Labelled N-Acetyl-S-(carbamoylethyl)-L-cysteine (A171870). N-Acetyl-S-(carbamoylethyl)-L-cysteine is the urinary metabolite of Acrylamide (AA). Acrylamide is formed during the heating of food and is classified as a genotoxic carcinogen. References Besaratinia, A., et al.: Mutat. Res., 80, 31 (2005), Bjellaas, T., et al.: Xenobiotica, 35, 1003 (2005), Bjellaas, T., et al.: Food Chem. Toxicol., 45, 1020 (2007), Bjellaas, T., et al.: Toxicol. Sci., 98, 110 (2007),

CAS 1795786-57-0

AAMA-d3

N-Acetyl-S-(carbamoylethyl)-L-cysteine-d3

Ref: TR-A171872