Skip to Content
Merck

Key Documents

View All Documentation

185868

N,N-Diethylaniline

≥99%

Synonym(s):

DEA

Sign In to View Organizational & Contract Pricing.

Select a Size

Change View

About This Item

Linear Formula:
(C2H5)2NC6H5
CAS Number:
91-66-7
Molecular Weight:
149.23
NACRES:
NA.22
PubChem Substance ID:
24851184
eCl@ss:
39030426
UNSPSC Code:
12352100
EC Number:
202-088-8
MDL number:
MFCD00009042
Beilstein/REAXYS Number:
742483
Assay:
≥99%
Form:
liquid
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist

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.)

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-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.

Still not finding the right product?

Explore all of our products under N,N-Diethylaniline

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

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

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
06420HJ
01630AJ
14706LH
S40285
06231JE

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

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

Visit the Document Library

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
View All Related Papers