345667-02-9

Basic information

• Product Name: N-[4-(4-tert-butylphenyl)phenyl]hydroxylamine
• Synonyms: [1,1'-biphenyl]-4-amine, 4'-(1,1-dimethylethyl)-N-hydroxy-; 4'-tert-Butyl-N-hydroxybiphenyl-4-amine
• CAS NO: 345667-02-9
• Molecular Formula: C₁₆H₁₉NO
• Molecular Weight: 241.3282
• Mol File: 345667-02-9.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 373.8°C at 760 mmHg
• Flash Point: 110.6°C
• Density: 1.087g/cm³
• Vapor Pressure: 3E-06mmHg at 25°C
• Refractive Index: 1.598
• CAS DataBase Reference: N-[4-(4-tert-butylphenyl)phenyl]hydroxylamine(CAS DataBase Reference)
• NIST Chemistry Reference: N-[4-(4-tert-butylphenyl)phenyl]hydroxylamine(345667-02-9)
• EPA Substance Registry System: N-[4-(4-tert-butylphenyl)phenyl]hydroxylamine(345667-02-9)

Safety Data

• Hazardous Substances Data: 345667-02-9(Hazardous Substances Data)

Upstream product

• 279242-11-4 4'-tert-butyl-4-nitrobiphenyl 

Relevant articles and documents

Mutagenicity in Salmonella typhimurium TA98 and TA100 of nitroso and respective hydroxylamine compounds

Five aromatic nitroso compounds were prepared and their mutagenicity in Salmonella typhimurium strains TA98 and TA100 compared with that of the corresponding hydroxylamines and the previously studied nitroarenes. A remarkable correspondence of the dose-response curves was observed between the nitroso and the respective hydroxylamine compounds. This effect could be observed in TA98 and TA100. It was only marginally dependent on the metabolical activation by rat liver S9-mix. Even the presence of a bulky alkyl substituent either near to the functional group, or far away from it, previously shown to considerably influence the mutagenic properties of nitroarenes, does not remarkably affect the properties of the nitroso and hydroxylamine species. The similarity between the latter two is likely to be due to a fast reduction of the nitrosoarenes to the hydroxylamine species under the test conditions. It seems that enzymes are not responsible for that reduction step, because sterical crowding near the functional group does not influence that behaviour. The test results of the aromatic hydroxylamines bearing a bulky substituent show that there are at least two ways to influence the mutagenicity of an aromatic nitro compound by such a group. A substituent near the functional group (ortho-position) disturbs the enzymatic reduction of the nitro group, because 3-tert-butyl-4-hydroxylaminobiphenyl and its corresponding nitroso compound are highly mutagenic, whereas 3-tert-butyl-4-nitrobiphenyl was previously shown to be inactive even after addition of S9-mix. In contrast, 4′-tert-butyl-4-hydroxylaminobiphenyl with the tert-butyl group "far away" from the hydroxylamino functionality clearly shows decreased mutagenic activity suggesting a different influence of a substituent in that position. In addition, the substance shows only little cell toxicity even at higher concentrations. Both effects could be due to a reduced effective dose of the hydroxylamine in the cells compared to the non-alkylated compound, caused by a faster degradation of the hydroxylamine or a hindered interaction between that substance and the cells.