Merck
CN

461121

Sigma-Aldrich

对甲苯胺

99%

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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:
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

1 hPa ( 42 °C)
7 hPa ( 68 °C)

检测方案

99%

形式

powder, crystals or chunks

自燃温度

899 °F

expl. lim.

6.6 %

bp

200 °C (lit.)

mp

41-46 °C (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-甲苯胺是一种芳族胺。可以通过均相液-液萃取和离子迁移谱(HLLE-IMS)在水样品中对其进行检测。

应用

p-甲苯胺可用于测定在非吸烟者和吸烟者(金色或黑色香烟)中芳香胺的血红蛋白加合物。 通过与水杨醛缩合,它可用于制备双齿席夫碱配体。

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

储存分类代码

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

WGK

WGK 3

闪点(°F)

188.6 °F - closed cup

闪点(°C)

87 °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

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Amin Ashori et al.
Bulletin of environmental contamination and toxicology, 94(4), 474-478 (2014-11-28)
In this research, homogeneous liquid-liquid extraction followed by ion mobility spectrometry (HLLE-IMS) with corona discharge ionization source has been developed for the determination of p-toluidine. The analyte was extracted by single-phase extraction in a ternary solvent system and then the
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)
M S Bryant et al.
Proceedings of the National Academy of Sciences of the United States of America, 85(24), 9788-9791 (1988-12-01)
Hemoglobin adducts of 15 aromatic amines were determined in nonsmokers and smokers of blond- or black-tobacco cigarettes living in Turin, Italy. The subjects were all males age 55 or less and were representative of the population previously examined in a
J C Kennelly et al.
Mutation research, 137(1), 39-45 (1984-07-01)
The conventional Ames assay metabolising system was confirmed to be deficient in its ability to N-acetylate. This may render the test less sensitive to compounds which normally have an acetylation step during their in vivo activation to carcinogens. The addition
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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