bis[(2H5)benzyl](nitroso)amine

• ChemBase ID: 175441
• Molecular Formular: C14H14N2O
• Molecular Mass: 226.27376
• Monoisotopic Mass: 226.11061308
• SMILES: c1(CN(Cc2ccccc2)N=O)ccccc1
• Canonical SMILES: O=NN(Cc1ccccc1)Cc1ccccc1
• InChI: InChI=1S/C14H14N2O/c17-15-16(11-13-7-3-1-4-8-13)12-14-9-5-2-6-10-14/h1-10H,11-12H2
• InChIKey: RZJLAUZAMYYGMS-UHFFFAOYSA-N

NAMES AND DATABASE IDS

Names

• IUPAC name: bis[(^2H₅)benzyl](nitroso)amine
• IUPAC Traditional name: bis[(^2H₅)benzyl](nitroso)amine
• Synonyms: N-Nitroso-N-(phenylmethyl)benzenemethanamine-d10; Dibenzylnitrosamine-d10; N,N-Dibenzylnitrosamine-d10; NSC 338-d10; Nitrosodibenzylamine-d10; N-Nitrosodibenzylamine-d10

Database IDs

• PubChem SID: 164231351
• PubChem CID: 71751123

CALCULATED PROPERTIES

• H Acceptors: 2
• H Donor: 0
• LogD (pH = 5.5): 3.4873204
• LogD (pH = 7.4): 3.487557
• Log P: 3.48756
• Molar Refractivity: 69.2757 cm^3
• Polarizability: 26.127275 Å^3
• Polar Surface Area: 32.67 Å^2
• Rotatable Bonds: 5
• Lipinski's Rule of Five: true

DETAILS

Toronto Research Chemicals - N525452

Labelled N-Nitrosodibenzylamine. N-Nitrosodibenzylamine (NDBzA) is mutagenic to Salmonella typhimurium and induces DNA strand breaks in isolated rat hepatocytes.

REFERENCES

• Dunn, W. et al.: Bioorg. Chem., 10, 29 (1981)
• Rose, S. et al.: J. Med. Chem., 25, 769 (1981)
• Basak, S. et al.: J. Pharm. Sci., 73, 429 (1981)
• Zielenska, M. et al.: Mutation Res., 180, 11 (1981)