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Merck

185868

Sigma-Aldrich

N,N-二乙基苯胺

≥99%

别名:

DEA

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About This Item

线性分子式:
(C2H5)2NC6H5
CAS号:
分子量:
149.23
Beilstein:
742483
EC號碼:
MDL號碼:
分類程式碼代碼:
12352100
eCl@ss:
39030426
PubChem物質ID:
NACRES:
NA.22

蒸汽密度

5.2 (vs air)

品質等級

蒸汽壓力

1 mmHg ( 49.7 °C)

化驗

≥99%

形狀

liquid

自燃溫度

1166 °F

折射率

n20/D 1.542 (lit.)

bp

217 °C (lit.)

mp

−38 °C (lit.)

溶解度

water: soluble 1g in 70ml at 12 °C
alcohol: slightly soluble
chloroform: slightly soluble
diethyl ether: slightly soluble

密度

0.938 g/mL at 25 °C (lit.)

SMILES 字串

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 密鑰

GGSUCNLOZRCGPQ-UHFFFAOYSA-N

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一般說明

N,N-二乙基苯胺与富勒烯形成电荷转移络合物

應用

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

訊號詞

Danger

危險分類

Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Aquatic Chronic 2 - Skin Irrit. 2 - STOT RE 2 Oral

儲存類別代碼

6.1C - Combustible, acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

水污染物質分類(WGK)

WGK 2

閃點(°F)

190.4 °F - closed cup

閃點(°C)

88 °C - closed cup

個人防護裝備

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter


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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
Fumihiro Ito et al.
Organic & biomolecular chemistry, 3(4), 674-681 (2005-02-11)
A convergent synthesis of kwakhurin (5), a characteristic estrogen-like isoflavone of Pueraria mirifica(Leguminosae), is described. Isoflavone skeleton 31 was constructed by Suzuki-Miyaura coupling of 3-bromochromone 26 (AC-ring) and arylboronic acid 30 (B-ring) in the presence of TBAB as an additive.
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
Photophysical properties of fullerenes and fullerene/N, N-diethylaniline charge-transfer complexes.
Wang Y.
The Journal of Physical Chemistry, 96(2), 764-767 (1992)
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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

实验方案

HPLC Analysis of Aniline Homologs on Discovery® C18

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