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About This Item
Empirical Formula (Hill Notation):
C12H11N
CAS Number:
Molecular Weight:
169.22
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
Assay:
97%
Form:
solid
Quality Level
assay
97%
form
solid
mp
28-33 °C
functional group
phenyl
SMILES string
Nc1cccc(c1)-c2ccccc2
InChI
1S/C12H11N/c13-12-8-4-7-11(9-12)10-5-2-1-3-6-10/h1-9H,13H2
InChI key
MUNOBADFTHUUFG-UHFFFAOYSA-N
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
>230.0 °F - closed cup
flash_point_c
> 110 °C - closed cup
Regulatory Information
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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 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
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
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 716448-1G | 04061825768755 |
