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A42409

Sigma-Aldrich

2-Aminobiphenyl

≥96.5% purity, powder or crystals

Sinónimos:

2-Biphenylylamine, 2-Phenylaniline

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About This Item

Fórmula lineal:
C6H5C6H4NH2
Número de CAS:
90-41-5
Peso molecular:
169.22
Beilstein/REAXYS Number:
471874
EC Number:
201-990-9
MDL number:
MFCD00007701
UNSPSC Code:
12171500
PubChem Substance ID:
24890839
NACRES:
NA.47

product name

2-Aminobiphenyl, ≥96.5% (GC)

vapor density

5.8 (vs air)

Quality Level

100

assay

≥96.5% (GC)

form

powder or crystals

autoignition temp.

842 °F

technique(s)

titration: suitable

impurities

<0.1% 4-aminobiphenyl

color

brown
 off-white to yellow

bp

299 °C (lit.)

mp

47-50 °C (lit.)

solubility

water: insoluble

density

1.16 g/cm3 at 21 °C

application(s)

diagnostic assay manufacturing
hematology
histology

storage temp.

room temp

SMILES string

Nc1ccccc1-c2ccccc2

InChI

1S/C12H11N/c13-12-9-5-4-8-11(12)10-6-2-1-3-7-10/h1-9H,13H2

InChI key

TWBPWBPGNQWFSJ-UHFFFAOYSA-N

Gene Information

human ... UGT1A4(54657)

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General description

2-Aminobiphenyl is a substrate for UGTs (UDP-glucuronosyltransferases), including UGT1A4, UGT2B13 and UGT2B16.

pictograms

Health hazardExclamation mark
GHS08,GHS07

signalword

Warning

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Chronic 3 - Carc. 2

Storage Class

11 - Combustible Solids

wgk_germany

WGK 2

flash_point_f

307.4 °F - closed cup

flash_point_c

153 °C - closed cup

ppe

Eyeshields, Gloves, type P3 (EN 143) respirator cartridges

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Certificados de análisis (COA)

Lot/Batch Number
SDBB0385
SDBB1036
STBL3323
STBK8194
STBK9634

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Y Yamazoe et al.
Xenobiotica; the fate of foreign compounds in biological systems, 14(7), 549-552 (1984-07-01)
The involvement of four forms of cytochrome P-450 in the activation of the promutagens, 3-amino-1-methyl-5H-pyrido[4,3-b]indole (Trp-P-2), 2-amino-6-methyl-dipyrido[1,2-a:3',2'-d]imidazole (Glu-P-1), 2-amino-3-methylimidazo[4,5-f]quinoline (IQ), 2-aminofluorene and 4-aminobiphenyl has been investigated using a Salmonella test system. A high-spin form, P-448 II-a, catalysed the activation of
S Kimura et al.
Carcinogenesis, 20(9), 1825-1830 (1999-09-02)
4-Aminobiphenyl (4-ABP), a potent carcinogen in rodents (liver cancer) and human (bladder cancer), is found as an environmental contaminant and in tobacco smoke. Hemoglobin adducts and lung DNA adducts of 4-ABP are found in tobacco smokers. In vitro metabolism studies
Identification of the rabbit liver UDP-glucuronosyltransferase catalyzing the glucuronidation of 4-ethoxyphenylurea (dulcin).
Uesawa Y, et al.
Drug Metabolism and Disposition, 32, 1476-1481 (2004)
R Harzmann et al.
Urologia internationalis, 35(5), 340-350 (1980-01-01)
It takes 24 months to induce preinvasive carcinomas in the urinary bladder of dogs as reported in the literature. The transplantation of chemically induced carcinomas has never been successful. Therefore, it was looked for methods which enable a shortening of
K M Abdo et al.
Fundamental and applied toxicology : official journal of the Society of Toxicology, 2(5), 201-210 (1982-09-01)
Diets containing 0.1 or 0.3% 2-biphenylamine hydrochloride were fed to groups of 50 Fischer 344 rats and 50 B6C3F1 mice of each sex for 104-106 weeks. Mean body weights of high-dose rats of both sexes and of low-dose male rats
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