461121
对甲苯胺
99%
别名:
4-氨基甲苯, 4-甲基苯胺
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关于此项目
线性分子式:
CH3C6H4NH2
化学文摘社编号:
分子量:
107.15
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
203-403-1
Beilstein/REAXYS Number:
471281
MDL number:
Assay:
99%
Bp:
200 °C (lit.)
Vapor pressure:
1 hPa ( 42 °C), 7 hPa ( 68 °C)
InChI key
RZXMPPFPUUCRFN-UHFFFAOYSA-N
InChI
1S/C7H9N/c1-6-2-4-7(8)5-3-6/h2-5H,8H2,1H3
SMILES string
Cc1ccc(N)cc1
vapor density
3.9 (vs air)
vapor pressure
1 hPa ( 42 °C), 7 hPa ( 68 °C)
assay
99%
form
powder, crystals or chunks
autoignition temp.
899 °F
expl. lim.
6.6 %
bp
200 °C (lit.)
mp
41-46 °C (lit.)
density
0.973 g/mL at 25 °C (lit.)
Quality Level
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General description
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。
Application
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。
signalword
Danger
Hazard Classifications
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
存储类别
6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials
wgk
WGK 3
flash_point_f
188.6 °F - closed cup
flash_point_c
87 °C - closed cup
ppe
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
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
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
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