
CAS 924-16-3: N-Nitrosodibutylamine
Formula:C8H18N2O
InChI:InChI=1S/C8H18N2O/c1-3-5-7-10(9-11)8-6-4-2/h3-8H2,1-2H3
InChI key:InChIKey=YGJHZCLPZAZIHH-UHFFFAOYSA-N
SMILES:N(CCCC)(CCCC)N=O
Synonyms:- 1-Butanamine, N-butyl-N-nitroso-
- Dibutylamine, N-nitroso-
- Di-n-butylnitrosamine
- N-Butyl-N-nitroso-1-butanamine
- Dibutylnitrosamine
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GB/T 24153-2009 Nitrosamines Mixture 137 100 µg/mL in Methanol
CAS:Controlled ProductColor and Shape:MixtureN-Nitroso-di-n-butylamine 10 µg/mL in Methanol
CAS:Controlled ProductFormula:C8H18N2OColor and Shape:Single SolutionMolecular weight:158.24N-Nitroso-Di-N-Butylamine (NDBA)
CAS:Formula:C8H18N2OColor and Shape:Yellow LiquidMolecular weight:158.25Nitrosamines Mixture 1013 2000 µg/mL in Dichloromethane
CAS:Controlled ProductFormula:C4H8N2O2Color and Shape:MixtureMolecular weight:116.12N-Nitroso-di-n-butylamine
CAS:N-Nitroso-di-n-butylamine is a nitrosamine that is a product of wastewater treatment. It has been shown to inhibit mitochondrial function and induce liver lesions in rats at high doses. N-Nitroso-di-n-butylamine is structurally similar to the natural substrate ribose, which leads to inhibition of xanthine oxidase, an enzyme involved in purine metabolism. The structural analysis revealed the presence of reactive sites that are susceptible to attack by nucleophiles, such as hydroxyl radicals or hydrogen peroxide. This indicates that N-Nitroso-di-n-butylamine may be a precursor for other carcinogenic compounds. NADH is reduced by NADH dehydrogenase (complex I) in mitochondria to produce NAD+, which subsequently donates electrons to the electron transport chain and generates ATP. The ability of NNDB to inhibit complex I activity was assessed using hl60Formula:C8H18N2OPurity:Min. 95%Molecular weight:158.24 g/mol