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Merck
CN

236314

Sigma-Aldrich

对甲苯胺

99.6%

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别名:
4-氨基甲苯, 4-甲基苯胺
线性分子式:
CH3C6H4NH2
CAS号:
分子量:
107.15
Beilstein:
471281
EC 号:
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22

蒸汽密度

3.9 (vs air)

质量水平

蒸汽压

0.26 mmHg ( 25 °C)
0.66 mmHg ( 38 °C)

检测方案

99.6%

形式

crystalline

自燃温度

899 °F

expl. lim.

6.6 %

pH值(酸碱度)

7.8 (7 g/L)

bp

200 °C (lit.)

mp

41-46 °C (lit.)

溶解性

water: soluble 135 part(lit.)
acetone: freely soluble(lit.)
alcohol: freely soluble(lit.)
carbon disulfide: freely soluble(lit.)
diethyl ether: freely soluble(lit.)
methanol: freely soluble(lit.)
oil: freely soluble(lit.)

密度

0.973 g/mL at 25 °C (lit.)

SMILES字符串

Cc1ccc(N)cc1

InChI

1S/C7H9N/c1-6-2-4-7(8)5-3-6/h2-5H,8H2,1H3

InChI key

RZXMPPFPUUCRFN-UHFFFAOYSA-N

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一般描述

p-甲苯胺可与儿茶酚胺发生氧化偶联反应,以在流动注射-分光光度法测定儿茶酚胺类药物过程中形成橙色水溶性染料

应用

p-甲苯胺已用于制备:
  • 芳香族偶氮化合物
  • 双齿Schiff碱配体(通过与水杨醛缩合)

警示用语:

Danger

危险分类

Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Aquatic Acute 1 - Aquatic Chronic 2 - Carc. 2 - Eye Irrit. 2 - Skin Sens. 1A

WGK

WGK 3

闪点(°F)

closed cup

闪点(°C)

closed cup

个人防护装备

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

法规信息

危险化学品

分析证书(COA)

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Flow injection-spectrophotometeric determination of some catecholamine drugs in pharmaceutical preparations via oxidative coupling reaction with< i> p</i>-toluidine and sodium periodate.
Abdulrahman LK, et al.
Analytica Chimica Acta, 538(1), 331-335 (2005)
Ruthenium (II) complexes containing bidentate Schiff bases and their antifungal activity.
Dharmaraj N, et al.
Transition Met. Chem. (London), 26(1-2), 105-109 (2001)
Paul G Stevenson et al.
Journal of chromatography. A, 1218(45), 8255-8263 (2011-10-11)
Several simple techniques are presented for the identification of the boundaries of chromatographic peaks. These methods provide a significant reduction in the time needed to perform the rapid, automatic calculation of the central peak moments and to evaluate the quality
Shunji Ito et al.
The Journal of organic chemistry, 70(6), 2285-2293 (2005-03-12)
[reaction: see text] N,N-Di(6-azulenyl)-p-toluidine (1a) and N,N,N',N'-tetra(6-azulenyl)-p-phenylenediamine (2a) and their derivatives with 1,3-bis(ethoxycarbonyl) substituents on each 6-azulenyl group (1b and 2b) were prepared by Pd-catalyzed amine azulenylation and characterized as a study into new aromatic amines for multistage amphoteric redox
D R Doerge et al.
Chemical research in toxicology, 4(5), 556-560 (1991-09-01)
The metabolism of three arylamine substrates by H2O2 in the presence of each of the peroxidative enzymes chloroperoxidase (CPX) and pea seed peroxygenase (PSM) was conducted with normal H2O2 and with 18O-labeled H2O2. The resulting C-nitroso aromatic metabolites were examined

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