716448
3-Aminobiphenyl
97%
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1 G
MXP 2,266.00
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1 G
MXP 2,266.00
About This Item
Fórmula empírica (notación de Hill):
C12H11N
Número de CAS:
Peso molecular:
169.22
Número MDL:
Código UNSPSC:
12352100
ID de la sustancia en PubChem:
NACRES:
NA.22
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Ensayo
97%
Formulario
solid
mp
28-33 °C
grupo funcional
phenyl
cadena SMILES
Nc1cccc(c1)-c2ccccc2
InChI
1S/C12H11N/c13-12-8-4-7-11(9-12)10-5-2-1-3-6-10/h1-9H,13H2
Clave InChI
MUNOBADFTHUUFG-UHFFFAOYSA-N
Categorías relacionadas
Palabra de señalización
Warning
Frases de peligro
Consejos de prudencia
Clasificaciones de peligro
Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Órganos de actuación
Respiratory system
Código de clase de almacenamiento
11 - Combustible Solids
Clase de riesgo para el agua (WGK)
WGK 3
Punto de inflamabilidad (°F)
>230.0 °F - closed cup
Punto de inflamabilidad (°C)
> 110 °C - closed cup
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J W Gorrod et al.
Anticancer research, 6(4), 729-731 (1986-07-01)
The metabolism of 3-aminobiphenyl (3-ABP) and 3-acetamidobiphenyl (3-AABP) has been studied using fortified rat liver microsomal preparations. Metabolites in concentrates of ether extracts from hepatic microsomal preparations were analysed by TLC and GLC. The metabolites were characterised by a comparison
M Maclure et al.
American journal of public health, 79(10), 1381-1384 (1989-10-01)
The hypothesis that involuntary exposure to tobacco smoke--passive smoking--results in greater risk of cancer was assessed by measuring the levels of two known carcinogens in the blood of 57 nonsmokers with varying degrees of involuntary exposure, including six heavily exposed
J Esteban Castelao et al.
International journal of cancer, 110(3), 417-423 (2004-04-20)
Previous epidemiological studies of fruit and vegetable intake and bladder cancer risk have yielded inconsistent results, especially with respect to the role of cigarette smoking as a possible modifier of the diet-bladder cancer association. A population-based case-control study was conducted
M Kajbaf et al.
European journal of drug metabolism and pharmacokinetics, 12(4), 285-290 (1987-10-01)
[14C] 2-Aminobiphenyl is predominantly metabolised in vivo to 3- and 5-hydroxy conjugated derivatives in all species. In some species, 2-aminobiphenyl is also excreted to a small extent as N-conjugated derivatives. Renal excretion accounts for about 30-40% of the administered dose
Mohamadi Sarkar et al.
Toxicology and applied pharmacology, 213(3), 198-206 (2006-01-13)
Some aromatic amines are considered to be putative bladder carcinogens. Hemoglobin (Hb) adducts of 3-aminobiphenyl (3-ABP) and 4-aminobiphenyl (4-ABP) have been used as biomarkers of exposure to aromatic amines from cigarette smoke. One of the goals of this study was
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