112763
二苯胺
99%, ReagentPlus®
别名:
N-Phenylbenzenamine, DBA, DFA, DPA
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关于此项目
线性分子式:
(C6H5)2NH
化学文摘社编号:
分子量:
169.22
NACRES:
NA.21
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
204-539-4
MDL number:
Beilstein/REAXYS Number:
508755
Assay:
99%
产品名称
二苯胺, ReagentPlus®, 99%
InChI key
DMBHHRLKUKUOEG-UHFFFAOYSA-N
InChI
1S/C12H11N/c1-3-7-11(8-4-1)13-12-9-5-2-6-10-12/h1-10,13H
SMILES string
N(c1ccccc1)c2ccccc2
vapor density
5.82 (vs air)
vapor pressure
1 mmHg ( 108 °C)
product line
ReagentPlus®
assay
99%
autoignition temp.
1175 °F
bp
302 °C (lit.)
mp
50-53 °C (lit.)
solubility
water: insoluble
Quality Level
Gene Information
human ... UGT1A4(54657)
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General description
二级芳香胺苯胺是苯胺的 N -取代衍生物。
Application
二苯胺可用于制备二苯胺试剂，通过比色法定量测定各种生物来源的核酸 (DNA)。它可以通过电化学和化学聚合的方法制备聚二苯胺 。也可作为气相色谱-质谱法测定毛发尼古丁的内标物。
Legal Information
ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany
signalword
Danger
Hazard Classifications
Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - STOT RE 2
target_organs
Kidney,Liver,spleen
存储类别
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
wgk
WGK 3
ppe
Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges
法规信息
危险化学品
此项目有
"Determination of hair nicotine by gas chromatography?mass spectrometry"
Man NC, et al
Journal of Chromatography. B, Analytical Technologies in the Biomedical and Life Sciences, 877(03), 339-342 (2009)
An improved diphenylamine method for the estimation of deoxyribonucleic acid.
Giles KW and Myers A.
Nature, 206(4979) , 93-93 (1965)
Soluble and methane sulfonic acid doped poly (diphenylamine)-synthesis and characterization.
Wen T-C, et al.
Materials Letters, 57(2), 280-290 (2002)
A study of the conditions and mechanism of the diphenylamine reaction for the colorimetric estimation of deoxyribonucleic acid.
K BURTON
The Biochemical journal, 62(2), 315-323 (1956-02-01)
John G Albeck et al.
Molecular cell, 49(2), 249-261 (2012-12-12)
The EGF-stimulated ERK/MAPK pathway is a key conduit for cellular proliferation signals and a therapeutic target in many cancers. Here, we characterize two central quantitative aspects of this pathway: the mechanism by which signal strength is encoded and the response
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