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185868

Sigma-Aldrich

N,N-Diethylaniline

≥99%

Sinónimos:

DEA

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About This Item

Fórmula lineal:
(C2H5)2NC6H5
Número de CAS:
91-66-7
Peso molecular:
149.23
Beilstein/REAXYS Number:
742483
EC Number:
202-088-8
MDL number:
MFCD00009042
UNSPSC Code:
12352100
eCl@ss:
39030426
PubChem Substance ID:
24851184
NACRES:
NA.22

vapor density

5.2 (vs air)

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.)

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

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General description

N,N-Diethylaniline forms charge transfer complex with fullerenes.

Application

N,N-Diethylaniline was used in one-pot synthesis of oxazol-5(4H)-ones. It was used in the synthesis of azo disperse dyes. It was used to prepare 6′-prenylisoflavone via Claisen rearrangement.

signalword

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

Storage Class

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

wgk_germany

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

Certificados de análisis (COA)

Busque Certificados de análisis (COA) introduciendo el número de lote del producto. Los números de lote se encuentran en la etiqueta del producto después de las palabras «Lot» o «Batch»

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4,N,N-Trimethylaniline purum, ≥98.0% (GC)

Sigma-Aldrich

41700

4,N,N-Trimethylaniline

DAF-FM DA solution 5 mM in DMSO, ≥97% (HPLC)

Sigma-Aldrich

D2321

DAF-FM DA solution

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
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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