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51788

Supelco

Aniline

analytical standard

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About This Item

Formula condensata:
C6H5NH2
Numero CAS:
62-53-3
Peso molecolare:
93.13
Beilstein:
605631
Numero CE:
200-539-3
Numero MDL:
MFCD00007629
Codice UNSPSC:
41116107
ID PubChem:
329757742
NACRES:
NA.24

Grado

analytical standard

Livello qualitativo

100

Densità del vapore

3.22 (185 °C, vs air)

Tensione di vapore

0.7 mmHg ( 25 °C)

Saggio

≥99.5% (GC)

Temp. autoaccensione

1139 °F

Durata

limited shelf life, expiry date on the label

Limite di esplosione

11 %

tecniche

HPLC: suitable
gas chromatography (GC): suitable

Impurezze

≤0.1% water
<0.03% nitrobenzene (C6H5NO2)

Indice di rifrazione

n20/D 1.586 (lit.)
n20/D 1.586

P. eboll.

184 °C (lit.)

Punto di fusione

−6 °C (lit.)

Densità

1.022 g/mL at 25 °C (lit.)

applicazioni

environmental

Formato

neat

Stringa SMILE

Nc1ccccc1

InChI

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

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Categorie correlate

Applicazioni

Methyl heneicosanoate has been used as an internal standard in the quantitative determination of fatty acids and their isomers composition using gas chromatography method of analysis (GC).
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Azioni biochim/fisiol

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.

Avvertenze

Danger

Classi di pericolo

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

Organi bersaglio

Blood

Codice della classe di stoccaggio

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

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

158.0 °F - closed cup

Punto d’infiammabilità (°C)

70 °C - closed cup

Dispositivi di protezione individuale

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

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Certificati d'analisi (COA)

Lot/Batch Number
BCCG0453
BCCF2378
BCCB9893
BCCB8358
BCCB2627

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Sigma-Aldrich

175692

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Supelco

78891

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Cyclohexyl-13C6-amine 99 atom % 13C

Sigma-Aldrich

603694

Cyclohexyl-13C6-amine

Teaching Innovations in Lipid Science (2007)
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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