蒸汽密度
3.9 (vs air)
质量水平
蒸汽压
1 hPa ( 42 °C)
7 hPa ( 68 °C)
方案
99%
表单
powder, crystals or chunks
自燃温度
899 °F
expl. lim.
6.6 %
沸点
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
此项目有
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
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
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