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Merck
CN

89630

对甲苯胺

for spectrophotometric det. of Au, Tl(III), W, ≥99.0%

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:
106-49-0
分子量:
107.15
UNSPSC Code:
12352200
NACRES:
NA.21
PubChem Substance ID:
329769756
EC Number:
203-403-1
Beilstein/REAXYS Number:
471281
MDL number:
MFCD00007906
Assay:
≥99.0% (GC)
≥99.0%
Technique(s):
UV/Vis spectroscopy: suitable
Bp:
200 °C (lit.)
Vapor pressure:
1 hPa ( 42 °C)
7 hPa ( 68 °C)

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产品名称

对甲苯胺, for spectrophotometric det. of Au, Tl(III), W, ≥99.0%

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

≥99.0% (GC)
≥99.0%

form

crystals

autoignition temp.

899 °F

quality

for spectrophotometric det. of Au, Tl(III), W

expl. lim.

6.6 %

technique(s)

UV/Vis spectroscopy: suitable

bp

200 °C (lit.)

mp

41-46 °C (lit.)
42-45 °C

solubility

ethanol: 1 g/10 mL (Hot)

density

0.973 g/mL at 25 °C (lit.)

Quality Level

100

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相关类别

Other Notes

用于 Tl(III)、Au 和 W 分光光度测定的试剂

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

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历史批次信息供参考:

分析证书(COA)

Lot/Batch Number
BCCN1334
BCCM8077
BCCM0715
BCCM2400
BCCK4226

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N. Mishra et al.
Analyst, 112, 1131-1131 (1987)
G. Pfrepper
Fresenius Journal of Analytical Chemistry, 193, 179-179 (1963)
K.S. Patel et al.
Analytical Chemistry, 58, 1547-1547 (1986)
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
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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