Skip to Content
Merck
All Photos(2)

Documents

185868

Sigma-Aldrich

N,N-Diethylaniline

≥99%

Synonym(s):

DEA

Sign Into View Organizational & Contract Pricing
All Photos(2)

About This Item

Linear Formula:
(C2H5)2NC6H5
CAS Number:
91-66-7
Molecular Weight:
149.23
Beilstein:
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)

Quality Level

100

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

Looking for similar products? Visit Product Comparison Guide

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.

Signal Word

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 Code

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

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Customers Also Viewed

Slide 1 of 2

1 of 2

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
Photophysical properties of fullerenes and fullerene/N, N-diethylaniline charge-transfer complexes.
Wang Y.
The Journal of Physical Chemistry, 96(2), 764-767 (1992)
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
View All Related Papers

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service