185868
N,N-二乙基苯胺
≥99%
别名:
DEA
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关于此项目
线性分子式:
(C2H5)2NC6H5
化学文摘社编号:
分子量:
149.23
NACRES:
NA.22
PubChem Substance ID:
eCl@ss:
39030426
UNSPSC Code:
12352100
EC Number:
202-088-8
MDL number:
Beilstein/REAXYS Number:
742483
Assay:
≥99%
Form:
liquid
vapor density
5.2 (vs air)
Quality Level
vapor pressure
1 mmHg ( 49.7 °C)
assay
≥99%
form
liquid
autoignition temp.
1166 °F
refractive index
n20/D 1.542 (lit.)
bp
217 °C (lit.)
mp
−38 °C (lit.)
solubility
water: soluble 1g in 70ml at 12 °C, alcohol: slightly soluble, chloroform: slightly soluble, diethyl ether: slightly soluble
density
0.938 g/mL at 25 °C (lit.)
functional group
amine
SMILES string
CCN(CC)c1ccccc1
InChI
1S/C10H15N/c1-3-11(4-2)10-8-6-5-7-9-10/h5-9H,3-4H2,1-2H3
InChI key
GGSUCNLOZRCGPQ-UHFFFAOYSA-N
General description
N,N-二乙基苯胺与富勒烯形成电荷转移络合物。
Application
N,N-二乙基苯胺被用于噁唑-5(4H)-酮的一锅合成。它被用于合成偶氮分散染料。它被用于通过克莱森重排制备6′-异戊二烯异黄酮。
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Danger
Hazard Classifications
Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Aquatic Chronic 2 - Skin Irrit. 2 - STOT RE 2 Oral
存储类别
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
wgk
WGK 2
flash_point_f
190.4 °F - closed cup
flash_point_c
88 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
法规信息
危险化学品
此项目有
Hikaru Fujita et al.
Chemical & pharmaceutical bulletin, 60(7), 907-912 (2012-07-14)
A method for one-pot synthesis of oxazol-5(4H)-ones has been developed using 4-(4,6-dimethoxy-1,3,5-triazin-2-yl)-4-methylmorpholinium chloride (DMT-MM), which is available for the activation of carboxylic acids in an aqueous solvent. The oxazolones were prepared by the N-acylation of amino acids with carboxylic acids
Sara Allin et al.
Health economics, policy, and law, 11(1), 39-65 (2015-05-23)
In spite of the vast number of studies measuring economic efficiency in health care, there has been little take-up of this evidence by policy-makers to date. This study provides an illustration of how a system-level study drawing on best practice
M R Yazdanbakhsh et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 77(5), 1084-1087 (2010-09-28)
A series of azo disperse dyes were synthesized by coupling reaction of N,N-diethylaniline, 2-anilinoethanol and N-phenyl-2,2'-iminodiethanol with diazotized aminothiazolyl derivatives as diazo components. These dyes have been prepared in good yields, and were characterized by UV-Vis, FT-IR and 1H NMR
全球贸易项目编号
| 货号 | GTIN |
|---|---|
| 185868-250ML | 04061838757661 |
| 185868-50ML | 04061836825546 |
| 185868-1L | 04061838757654 |