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716448

Sigma-Aldrich

3-Aminobiphenyl

97%

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About This Item

Empirical Formula (Hill Notation):
C12H11N
CAS Number:
Molecular Weight:
169.22
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Assay

97%

form

solid

mp

28-33 °C

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

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

>230.0 °F - closed cup

Flash Point(C)

> 110 °C - closed cup


Certificates of Analysis (COA)

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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
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
G Ronco et al.
British journal of cancer, 61(4), 534-537 (1990-04-01)
In a previous study we found that aromatic amines, particularly 4-aminobiphenyl, formed haemoglobin adducts at higher concentrations in the blood of smokers compared to non-smokers. We re-analyse here data on haemoglobin adducts of 14 aromatic amines in order to ascertain
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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