- can be
categorized as C-
nitroso compounds (e.g., nitrosoalkanes; R−N=O), S-
nitroso compounds (nitrosothiols; RS−N=O), N-
nitroso compounds (e.g., nitrosamines...
-
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...
-
Nitrosoproline is a
nitroso derivative of the
amino acid proline. v t e...
-
possible carcinogens N-nitrosodiethylamine, N-methylnitrosobutyric acid, or N-
nitroso-N-methyl-4-aminobutyric acid in the
active pharmaceutical ingredient (API)...
- N-Nitrosodimethylamine (NDMA), also
known as
dimethylnitrosamine (DMN), is an
organic compound with the
formula (CH3)2NNO. It is one of the
simplest members...
- for the
process of
converting organic compounds or
metal complexes into
nitroso derivatives, i.e.,
compounds containing the R−NO functionality. The synonymy...
- 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...
- N-
Nitroso-N-methylurea (NMU) is a
highly reliable carcinogen, mutagen, and teratogen. NMU is an
alkylating agent, and
exhibits its
toxicity by transferring...
- 1-
Nitroso-2-naphthol is an
organic compound with the
formula C10H6(NO)OH. It is one of
several possible nitrosonaphthols, and the most
studied for applications...
- that form N-
nitroso compounds. A prin****l
concern about sodium nitrite is Nitrosation/nitrosylation, the
formation of
carcinogenic nitroso-compounds in...
