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Merck
CN

V800060

Aniline

≥99%, liquid, suitable for analytical testing, Vetec™, LR grade

Synonym(s):

Aminobenzene, Benzenamine

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About This Item

Linear Formula:
C6H5NH2
CAS Number:
62-53-3
Molecular Weight:
93.13
UNSPSC Code:
12191502
PubChem Substance ID:
329829120
EC Number:
200-539-3
Beilstein/REAXYS Number:
605631
MDL number:
MFCD00007629
Assay:
≥99%
Grade:
LR
Bp:
184 °C (lit.)
Vapor pressure:
0.7 mmHg ( 25 °C)

Key Documents

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Product Name

Aniline, LR, ≥99%

InChI key

PAYRUJLWNCNPSJ-UHFFFAOYSA-N

InChI

1S/C6H7N/c7-6-4-2-1-3-5-6/h1-5H,7H2

SMILES string

Nc1ccccc1

grade

LR

vapor density

3.22 (185 °C, vs air)

vapor pressure

0.7 mmHg ( 25 °C)

product line

Vetec™

assay

≥99%

form

liquid

autoignition temp.

1139 °F

expl. lim.

11 %

dilution

(for analytical testing)

pH

8.8 (20 °C, 36 g/L)

bp

184 °C (lit.)

mp

−6 °C (lit.)

density

1.022 g/mL at 25 °C (lit.)

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Biochem/physiol Actions

The acute toxicity of aniline involves its activation in vivo to 4-hydroxyaniline and the formation of adducts with hemoglobin. In erythrocytes, this is associated with the release of iron and the accumulation of methemoglobin and the development of hemolytic anemia and inflammation of the spleen. Tumor formation is often observed in the spleen on prolonged administration.

Legal Information

Vetec is a trademark of Merck KGaA, Darmstadt, Germany

signalword

Danger

Hazard Classifications

Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Carc. 2 - Eye Dam. 1 - Muta. 2 - Skin Sens. 1 - STOT RE 1

target_organs

Blood

Storage Class

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

wgk

WGK 3

flash_point_f

158.0 °F - closed cup

flash_point_c

70 °C - closed cup

Regulatory Information

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Certificates of Analysis (COA)

Lot/Batch Number
MMBB4490
MMBB4611
MMBB4571
MMBB3872
MMBB3590

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Hongli Ji et al.
Molecular plant-microbe interactions : MPMI, 28(5), 519-533 (2015-01-22)
The nonprotein amino acid β-aminobutyric acid (BABA) is known to protect plants against various pathogens. The mode of action is relatively diverse and specific in different plant-pathogen systems. To extend the analysis of the mode of action of BABA to
S A Vaziri et al.
Pharmacogenetics, 11(1), 7-20 (2001-02-24)
Arylamines such as 2-naphthylamine and 4-aminobiphenyl are suspected human bladder procarcinogens that require bioactivation to DNA-reactive species to exert their carcinogenic potential. The goals of the present study were (i) to assay for the presence of the arylamine acetyltransferases NAT1
M Peluso et al.
Carcinogenesis, 21(2), 183-187 (2000-02-05)
The 'Mediterranean diet', a diet rich in cereals, fruit and vegetables, has been associated with lowering the risk of a variety of cancers of the digestive tract and the bladder. In a previous study, we showed that the high phenolic
J S Bus et al.
Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association, 25(8), 619-626 (1987-08-01)
Aniline and several structurally-related aromatic amines produce spleen tumours in rats given high doses of compound in 2-year bioassay studies. Evaluation of the pathogenesis of the splenic lesions and characterization of the disposition of radiolabelled aniline in animals suggests that
Conghui Tang et al.
Journal of the American Chemical Society, 134(46), 18924-18927 (2012-11-08)
A novel and efficient copper-catalyzed azidation reaction of anilines via C-H activation has been developed. This method, in which the primary amine acts as a directing group by coordinating to the metal center, provides ortho azidation products regioselectively under mild
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