Nitrosamine (redirect from N-nitroso) chemical structure R2N−N=O, where R is usually an alkyl group. They feature a nitroso group (NO+) bonded to a deprotonated amine. Most nitrosamines are carcinogenic... 11 KB (1,824 words) - 20:19, 29 March 2024 |
N-Nitrosodimethylamine (redirect from N-Methyl-N-nitroso-methanamine) N-Nitrosodimethylamine (NDMA), also known as dimethylnitrosamine (DMN), is an organic compound with the formula (CH3)2NNO. It is one of the simplest members... 25 KB (2,389 words) - 11:54, 10 April 2024 |
Nitrosation (section C-Nitroso compounds) converting organic compounds into nitroso derivatives, i.e., compounds containing the R-NO functionality. C-Nitroso compounds, such as nitrosobenzene... 3 KB (268 words) - 00:33, 29 August 2023 |
Due to the electronegativity difference between carbon and nitrogen, the nitroso group has a relatively strong -I effect, but not as strong as the nitro... 27 KB (2,728 words) - 23:10, 24 March 2024 |
that form N-nitroso compounds. A principal concern about sodium nitrite is Nitrosation/nitrosylation, the formation of carcinogenic nitroso-compounds in... 13 KB (1,371 words) - 18:23, 21 March 2024 |
Nitrosoproline (redirect from N-nitroso-L-proline) Nitrosoproline is a nitroso derivative of the amino acid proline. v t e... 1 KB (13 words) - 03:36, 18 December 2021 |
N-Nitroso-N-methylurea (NMU) is a highly reliable carcinogen, mutagen, and teratogen. NMU is an alkylating agent, and exhibits its toxicity by transferring... 5 KB (377 words) - 17:43, 30 March 2024 |