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149381

Sigma-Aldrich

2,6-Diethylaniline

98%

Synonym(s):

2-Amino-1,3-diethylbenzene

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About This Item

Linear Formula:
(C2H5)2C6H3NH2
CAS Number:
579-66-8
Molecular Weight:
149.23
Beilstein:
1423626
EC Number:
209-445-7
MDL number:
MFCD00007753
UNSPSC Code:
12352100
PubChem Substance ID:
24848950
NACRES:
NA.22

vapor pressure

0.02 mmHg ( 20 °C)

Quality Level

100

Assay

98%

refractive index

n20/D 1.545 (lit.)

bp

243 °C (lit.)

density

0.906 g/mL at 25 °C (lit.)

SMILES string

CCc1cccc(CC)c1N

InChI

1S/C10H15N/c1-3-8-6-5-7-9(4-2)10(8)11/h5-7H,3-4,11H2,1-2H3

InChI key

FOYHNROGBXVLLX-UHFFFAOYSA-N

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General description

The 2,6-diethylaniline complexes with iodine, as a sigma-acceptor, were studied spectrophotometrically in chloroform, dichloromethane and carbontetrachloride solutions.

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H302

Precautionary Statements

P264 - P270 - P301 + P312 - P501

Hazard Classifications

Acute Tox. 4 Oral

Storage Class Code

10 - Combustible liquids

WGK

WGK 2

Flash Point(F)

239.0 °F - closed cup

Flash Point(C)

115 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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S J Logusch et al.
Journal of agricultural and food chemistry, 47(5), 2125-2129 (1999-12-20)
Rat liver tissue homogenates were utilized for in vitro enzymatic conversion of 2,6-diethylaniline (DEA) to the important alachlor metabolite 4-amino-3,5-diethylphenyl sulfate (ADEPS), which was also generated as a radiolabeled standard for use in metabolism studies. ADEPS formation in rodents is
Q Li et al.
Mutation research, 395(2-3), 151-157 (1998-02-18)
N,N-Diethylaniline is a reagent used in organic synthesis and is an important intermediate in the manufacturing of dyes. To evaluate its genotoxicity, we examined whether it can induce sister chromatid exchanges (SCEs) in human lymphocytes. We found that N,N-diethylaniline significantly
A D Kligerman et al.
Mutation research, 441(1), 95-101 (1999-05-04)
Alachlor is a widely used herbicide for which there is significant human exposure, principally through groundwater contamination and inhalation. Because alachlor is purported to be carcinogenic and mutagenic, we initiated studies to determine if induced cytogenetic damage could be used
Yongxia Zhang et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 85(1), 134-138 (2011-11-01)
In this letter, we report the first observation of metal-enhanced exciplex fluorescence, observed from anthracene in the presence of diethylaniline. Anthracene in the presence of diethylaniline in close proximity to Silver Island Films (SIFs) shows enhanced monomer and exciplex emission
R Galati et al.
Anticancer research, 18(2A), 979-982 (1998-06-06)
In order to estimate the environmental risk of the use of Alachlor, experiments on laboratory animals were conducted. Alachlor and 2,6 diethylaniline content in blood serum was quantified. Three groups of male ACI/T rats and C3H/FEJ mice were treated with
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